CEE353 Civil Engineering Materials Lab Manual-Updated Fall 2019 (1)

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CEE353/CNE353 C IVIL E NGINEERING M ATERIALS CEE353/CNE353 C IVIL E NGINEERING M ATERIALS Laboratory Instruction Manual
* Please check every Monday for updated lab manual
C IVIL E NGINEERING M ATERIALS Table of Contents LAB 1: MEASUREMENT CONCEPTS ........................................................................................................... 1 LAB 2: TENSION TEST OF STEEL AND ALUMINUM (ASTM E-8) & CHARPY V-NOTCH IMPACT TEST ON STEEL (ASTM E23) ......................................................................................................................... 5 Part 1: Tension Test of Steel and Aluminum .............................................................................................. 5 Part 2: CHARPY V-NOTCH IMPACT TEST ON STEEL (ASTM E23) ................................................. ................................ 14 Part I: Rebound Hammer (ASTM C805) .................................................................................................... 15 Part II: Ultrasonic Pulse Velocity (UPV) testing (ASTM C597) .............................................................. 17 Part III: Image Analysis using ImageJ Software ...................................................................................... 20 LAB 4: VISCOSITY OF LIQUIDS ............................................................................................................ 23 LAB 5: FIBER-REINFORCED COMPOSITES AND CREEP OF POLYMERS ....................................... 32 LAB 6: COMPRESSION TESTING OF WOOD ....................................................................................... 38 LAB 7 & 8: AGGREGATES ............................................................................................................................. 43 PART I: Sieve Analysis (ASTM C136) ........................................................................................................ 43 PART II: Specific Gravity and Absorption of Coarse Aggregate (ASTM C127) ..................................... 46 PART III: Dry Rodded Unit Weight and Voids in Aggregate (ASTM C29) ............................................ 48 PART IV: Specific Gravity and Absorption of Fine Aggregate (ASTM C128) ........................................ 49 PART V: Moisture Content of Aggregate Stockpiles (ASTM C566) ........................................................ 51 PART VI: Uncompacted Void Content of Fine Aggregate (ASTM C1252) and Coarse Aggregate (AASHTO T 326) ........................................................................................................................................... 52 LAB 9: MIXING CONCRETE AND FRESH PCC PROPERTIES .............................................................. 56 PART I Concrete Mixing (by weight) ................................................................................................. 56 PART II: Slump Test of Freshly Mixed Portland cement Concrete (ASTM C143) ............................. 59 PART III: Air Content of Freshly Mixed Concrete by Pressure Method (ASTM C231) ....................... 61 PART IV: Making and Curing Concrete Cylinders and Beams (ASTM C31) ........................................ 63 LAB 10: HARDENED PROPERTIES OF PCC ........................................................................................ 66 PART I: Compressive Strength of Cylindrical Concrete Specimens (ASTM C39) ................................. 66 PART II: Flexural Strength of Concrete (ASTM C78) ............................................................................... 68 PART III: Splitting Tensile Strength of Cylindrical Concrete Specimens (ASTM C496) ...................... 71 PART IV: Ultrasonic Pulse Velocity ........................................................................................................... 72 LAB 11: ASPHALT CEMENT TESTING AND GYRATORY COMPACTION .......................................... 74 PART I: Viscosity Determination of Asphalt Using a Rotational Viscometer (ASTM D4402) ............ 74 PART II: Penetration Test of Asphalt Binder (ASTM D5) ....................................................................... 77 PART III: Dynamic Shear Modulus of Asphalt Cement (ASTM D7175) ............................................. 80 PART IV: Gyratory Compaction (ASTM D6925) ....................................................................................... 82 LAB 12: ASPHALT CONCRETE TESTING ................................................................................................. 87 PART I: Theoretical Maximum Specific Gravity of Hot Mix Asphalt (ASTM D2041) .......................... 87 PART II: Bulk Specific Gravity of Compacted Bituminous Mixtures (ASTM D2726) .......................... 89 10 LAB 3: MICROSTRUCTURE OF MATERIALS AND NDT (ASTM C597 & C805) CEE353/CNE353
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PART III: Mechanical Test .................................................................................................................... 94 Notes - For these labs you will need to review the ASTM or AASHTO standards prior to coming to the lab and when performing calculations. ASTM standards can be obtained digitally by going to http://library.lib.asu.edu/record=e1001646~S3 . AASHTO standards can be found in Knovel. - Discussion questions may be modified during the course of the semester. Always pay attention to the TA in lab sessions for changes to the discussion questions.
Page 1 LAB 1: MEASUREMENT CONCEPTS Significance: Today’s lab will let you examine some of the most commonly-used laboratory measurement devices in Civil Engineering Materials experiments. These devices will be utilized in the upcoming labs throughout the semester, and therefore it is important to gain a good understanding of their characteristics, capabilities, and use. Apparatus: - Load cell - Strain gage - Dial gage - Proving ring - Linear Variable Displacement Transducer (LVDT) - Length measurement tools. Prior to this lab go to the internet and look up a photograph of a load cell, strain gage, dial gage, proving ring, and LVDT and search to learn about the essential function and operation of each device looking specifically for the physical quantity that each device measures and the overall method by which this physical measurement is taken. For example you should know that a proving ring measures mass/force and does this based on measuring the elastic deformation of a ring and then using this deformation with a known relationship between ring deformation and mass. Also make sure that you are familiar with all terms that are given in the procedure, e.g., what is meant by range, sensitivity or any other unfamiliar terms. Procedure: 1. Examine the dial gage, note its sensitivity and range, and state where it would be used in a real-life application. 2. Examine the strain gage and comment on its use. 3. Examine the load cell and comment on its use. 4. Examine the LVDT and comment on its use. a. For the LVDT: Using the micrometer, adjust the displacement, recording the five values “to the left,” and four values “to the right” of the zero point (see Table 1-1). b. Keep the following in mind: - Ideally, the LVDT is “zeroed” when the micrometer reads exactly 0.500 inches. - One “rotation” of the micrometer is equal to 0.025 inches of displacement. 5. Examine the proving ring and attached dial gauge, and comment on its use. Fill out Table 1-2 below, and keep the following in mind: - Before you start measuring, make sure that the large hand is exactly on zero, and adjust it if necessary. - Note the initial position of the small hand of the dial gage. One full “rotation” of the large dial corresponds to one increment of movement on the small dial. - With the dial gage in the protective “cage,” carefully stack the weights on.
Page 2 - Before you measure the unknown weight, check once again that the large hand is exactly on zero. 6. For the given specimens of concrete (or asphalt), use the appropriate techniques to accurately measure the lengths and the diameters. Make a table, providing the dimensions of these members, along with the values that you would use if you are to report this to a client. Results and Calculations: - Fill out the tables below and include these tables in your lab report write-up. - For the LVDT experiment, plot the displacement as a function of the voltage. After plotting the points, develop an equation for the line that represents the voltage displacement relationship and calculate the R 2 for this relationship (Microsoft Excel can do this for you). Show the best fit equation along with the R-squared value in the plot you create. - For the Dial Gage experiment, plot the weight as a function of the dial gauge reading. Calculate the “unknown” weight, using the equation of the line you graphed under “Results.” Again, show the equation and R-squared value on your graph, and label, by hand, the “unknown” weight as a point on your graph. The only actual calculation you must show is solving for the unknown weight. Note that for the latter result, you must convert the dial gage readings to actual displacements (inches). Do not forget to label all axes (with units), and include an original chart title. Table 1-1: Displacement with Corresponding Voltage Readings Displacement (mm) Distance from Zero Point (mm) Voltage Reading (V) 3. 00 - 1.00 2. 00 - 2 .00 1. 00 - 3. 00 0 .00 - 4 .00 5. 00 1. 00 4. 00 = “Zero Point” 0.000 9. 00 5 . 00 8. 00 4. 00 7. 00 3. 00 6 . 00 2. 00
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Page 3 Table 1-2: Dial Gage Readings for Various Weights on Proving Ring Weight (lbs) Dial Gage Reading (increments) Deformation (in.) Unknown Weight Notes:
Page 4 Group Discussion: 1. What is meant by accuracy, precision, and sensitivity, and how was this demonstrated in this lab? 2. Briefly explain how the micrometer works (i.e. what one full rotation of the rod means, the relationship between “horizontal” and “vertical” increments on the micrometer, and how the distances are converted to a voltage measurement.) What is the relationship between voltage and displacement, as examined in the LVDT experiment? Were the voltage readings within the linear range of the LVDT? After taking a few readings, was the voltage reading still zero when you returned to 0.500 inches on the micrometer? Explain. 3. Explain how the dial gage and proving ring work. What does one full rotation of the “big arm” mean? What does one incremental movement of the “small arm” mean? What is the sensitivity and range of the dial gage used? Based on your collected data, how much does the “unknown” weight weigh, and does this value make sense? 4. Is there any discrepancy in your data? Do your graphs look like what you expected? If yes, explain why. If not, did you encounter any sources of error during the experiment? Explain. Individual Discussion: 1. Include a brief description (2-3 sentences) of each device you examined. Comment on its use and real-life application.
Page 5 LAB 2: TENSION TEST OF STEEL AND ALUMINUM (ASTM E-8) & CHARPY V-NOTCH IMPACT TEST ON STEEL (ASTM E23) Part 1: Tension Test of Steel and Aluminum Significance: In this lab, you will observe the uniaxial tension testing of aluminum and steel samples, according to ASTM E8 Tension Testing of Metallic Materials. From the results of the tests, you will be able to graphically represent the stress-strain relationship, compare the yield strength and ultimate strength of the two materials, determine elongation and reduction in cross-sectional area, and find the Young’s Modulus and rupture strength of each specimen. Tension test of steel and aluminum https://www.youtube.com/watch?v=D8U4G5kcpcM ( Note that the sample geometry in this video will be different than the one we use for the lab, but the process will be similar ) Apparatus: - Small aluminum and steel rods - Instron testing machine - Caliper - Extensometer - A computer to generate the data points during the test. Procedure: 1. An overview of what will happen in today’s lab: a. A testing machine will apply a uniaxial tensile load at a controlled rate. The machine will be connected to a computer that automatically provides numerical values for the changing stress and strain during the testing. (I will post this data on Blackboard for you to access later on.) b. Two test specimens, one aluminum and one steel, will be loaded into the machine. Axial load will be applied to the specimen at a controlled rate, and this will cause axial stress within the gage length of the specimen. c. An extensometer will measure the deformation of each specimen. 2. Before testing, perform these steps: a. Using a permanent marker, mark a line on each end of the specimen, just before the threads. This will be L 0 , the original gage length. b. Using the caliper, measure this gage length three times, and average the measurements to get a “true” length. Measure the diameter of the specimen in three different places (i.e. near the two ends and in the middle), and use the average of these measurements as the “actual” diameter, d 0 . Record all measurements, and convert them to millimeters.
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Page 6 A f A 0 A 0 c. Determine the initial cross-sectional area, A 0 , of the specimen, in square millimeters. 3. During testing, take note of the following: a. How does each specimen visibly change as load is being applied? b. Can you identify the yield point as the computer is generating the stress-strain curve? c. How long did it take each specimen to reach its rupture strength? 4. After testing: a. Determine the gage length after rupture, L f , of the specimen. Line up exactly the two ends of the ruptured specimen, and measure between the gage length lines you marked earlier. Again, take three measurements with the caliper, and use the average as the “true” value. b. Determine the final cross-sectional area, using the narrowest diameter of the ruptured specimen. Again, you will need to line up the two ends of the ruptured specimen to make this measurement. Calculations: - Calculate the average initial length (L 0 ) and average final length (L f ) for each specimen. - Determine the percent elongation using the following equation. L f L 0 % Elongation = 100 L 0 - Calculate the average initial cross-sectional area (A 0 ) and average final cross- sectional area (A f ) for each specimen. - Determine the percent reduction in cross-sectional area using the following equation. % Reduction in Cross-Sectional Area = 100 Results: - Summarize your individual and average elongation and cross-sectional area results in Table 2-1 . - Plot the stress-strain curve for each specimen. Label the axes appropriately. Estimate the yield strength using the offset method (Section 7.7.1) and a 0.2% offset. You can draw the required line by hand, but be neat and use a straight edge. Report the yield strength according to the method given in the standard. You only need to report values in the units of psi. - On the same graphs above locate the ultimate strength and the rupture strength on each curve. Neatly label the yield strength, ultimate strength, and rupture strength on your graphs. - For each specimen, find Young’s Modulus. One way to do this is to create a graph that shows only the linear portion of the stress-strain curve. Develop a best-fit line for these points, and label the equation for the line. The slope of this line is Young’s Modulus. If you use this method, you do NOT need to include these separate graphs
Page 7 in your report. You are only responsible for finding Young’s Modulus, using your method of choice. Summarize these results in
Page 8 - Table 2-2.
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Page 9 Table 2-1: Specimen Dimensions Property Steel Aluminum Length Before Test: After Test: Before Test: After Test: L 1 = L 1 = L 1 = L 1 = L 2 = L 2 = L 2 = L 2 = (in. or mm) L 3 = L 3 = L 3 = L 3 = L 0 = L f = L 0 = L f = Diameter d 1 = d 1 = d 1 = d 1 = d 2 = d 2 = d 2 = d 2 = and Area (in. and in. 2 or d 3 = d 3 = d 3 = d 3 = mm andmm 2 ) d 0 = d f = d 0 = d f = A 0 = A f = A f = A f =
Page 10 Table 2-2: Aluminum and Steel Properties Material Property Steel Aluminum Estimated 0.2% offset yield strength (psi or MPa) Tensile strength (psi or MPa) Rupture strength (psi or MPa) Young’s Modulus (psi or MPa) Percent elongation (%) Percent reduction of cross- sectional area (%) Type of failure (ductile vs. brittle) Group Discussion: 1. Compare the two specimens. As a minimum, include in this comparison the following items: a. Which material provided higher yield strength? b. Did each of the specimens exhibit ductile or brittle failure, and how do you know? c. What was the plastic range of each specimen (Plastic range = difference between yield strength and ultimate strength)? d. Which specimen had the higher percent elongation, and how does this relate to ductility? e. How different were the Young’s Moduli and the rupture strengths of the two specimens? Individual Discussion: 1. Research the density of steel and aluminum. Combine this information with the results you obtained to discuss the possible industrial applications of each material?
Page 11 Part 2: CHARPY V-NOTCH IMPACT TEST ON STEEL (ASTM E23) Purpose: In the Charpy V-Notch lab, students will investigate the energy absorbed by different V- Notch steel specimens using an impact-testing machine. See schematic below for reference. The amount of energy required to break a material is used to rate the material’s toughness. Toughness is a function of the material’s temperature. Students will perform the Charpy V- Notch test on four different specimens with properties as follows: - Specimen #1: Soaked in isopropyl alcohol and dry ice mixture for 1 hour prior to testing. Approximate testing temperature : -40 ° C - Specimen #2: Soaked in a mixture of 30% isopropyl alcohol, 70% water, and dry ice for 1 hour prior to testing. Approximate testing temperature: -20 ° C - Specimen #3: Soaked in ice-water (using “regular” ice) for 1 hour prior to testing. Approximate testing temperature: 4 ° C - Specimen #4: Heated in the oven for 1 hour before testing. Approximate testing temperature: 40 ° C Overview of Testing Apparatus: The impact test machine consists of a 30-kg (66.14- lb) pendulum that is raised to a given height and locked in place. The specimen sits in the center position of the hammer’s path, with the “V” notch facing away from the swing of the hammer. A knob is used to control when the hammer is released. Once the pendulum is in full swing, it can be stopped by a small button that creates friction, slowing down the hammer’s motion. The top of the machine has a scale readout to indicate the energy in ft-lbs. As the hammer swings, a small cantilever handle moves the readout mark. Safety Precautions: The hammer is extremely heavy and can seriously injure a student who happens to be standing at the wrong place during testing. Follow the TA’s instructions carefully during this lab. But you should also make sure to adhere to the following rules: 1. Do not approach the hammer while being released or while in swing. 2. Never stand in front of the hammer’s swing path. 3. Make sure that someone is holding up the hammer while specimens are placed in position. Procedure: 1. Before testing, each specimen’s dimensions (length, width, height) will be recorded. The recorded data set will be provided to the students in order to determine the length, width, and height expansions after testing. Source: http://www.twi.co.uk/twiimages/ faqplm005f1.gif Figure 2-1: Charpy Test Apparatus
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Page 12 2. To account for the effects of friction, the impact machine will be calibrated by performing a free swing energy dissipation measurement. The calibration procedure “zeroes” the testing machine. The gage mark from the free swing will be used as the “zero” energy mark. 3. A thermometer will be used to double check the actual temperature of each specimen prior to testing. 4. A tong will be used to remove each specimen from the medium and place into testing position. In the meantime, a student will have to hold the hammer for safety reasons. 5. The gage mark on the readout will be moved to the high end of the scale prior to each trial. The swinging motion will bring the gage mark back up, indicating the actual energy measurement. 6. The hammer will be set in full swing and will break the steel specimen in two upon impact. The broken specimen will be collected using the tong, and at room temperature height, width, and length will be measured and recorded. 7. The fracture pattern of each specimen will be observed. Feel free to take pictures of the fracture surface of each specimen and comment on the fracture surface. Calculations: All units must be in English customary. Show numerical calculations (with units) when finding energy absorbed by each steel specimen. Also note the “zeroed” value of the testing machine. Results: - Summarize your measurements in Table 2-3 and Table 2-4. - Create a temperature versus energy plot, where the energy dissipated is shown as a function of temperature. - Connect your four data points using a curve-fit, and label the ductile-to-brittle transition zone.
Page 13 Table 2-3: Specimen Dimensions Dimension Specimen 1 (at -40 ° C) Specimen 2 (at -20 ° C) Specimen 3 (at 4 ° C) Specimen 4 (at 40 ° C) Length L 0 L f ΔL Width W 0 W f ΔW Height H 0 H f ΔH Table 2-4: Specimen Measurements and Observations Specimen # Actual Temp. ( ° C) Energy (ft-lbs) Fracture Pattern 1 2 3 4 Notes
Page 14 Group Discussion: 1. What were the typical failure modes? 2. Describe the failure surface (pictures or diagrams would be helpful), and comment on how temperature influences the type of failure mode. 3. Describe how the dimensions of each specimen changed. Which of the specimens exhibited the largest/smallest deformation, and why? What does this suggest about the packing of the atoms (closely packed vs. loosely packed)? Individual Discussion: 1. What is the relationship between testing temperature and energy required to break the steel specimen? 2. What does temperature versus energy relationship suggest about the toughness of the material at different temperatures? Appendix: Include any handwritten observations/drawings/calculations that you did during lab. Your actual typed-up calculations should go in the “Calculations” section.
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Page 15 LAB 3: MICROSTRUCTURE OF MATERIALS AND NDT (ASTM C597 & C805) Purpose: In this lab, you will examine microstructure assessment and nondestructive testing concepts by doing the following tasks: Predict the strength of concrete using a Rebound Hammer; Predict the elastic modulus of a material from the wave transmissions through the material; and Back-calculate material constituents, void fractions, etc. from non- destructive measurements and Image Analysis software. Equipment and Materials: - Rebound hammer - UPV meter - Calipers and scale - Image J software (Specimens to be scanned) - Concrete, Porous Concrete and Asphalt Concrete Specimens Table 3-1: Specimen Properties Sample Weight (lb) Length (in.) Void Ratio Poisson’s Ratio Porous 0.15 OPC 0.20 Asphalt 0.35
Page 16 Part I: Rebound Hammer (ASTM C805) Overview of Testing Apparatus: The rebound hammer consists of a spring- loaded steel hammer that when released strikes a steel plunger in contact with the concrete surface. The spring-loaded hammer must travel with a consistent and reproducible velocity. The rebound distance of the steel hammer from the steel plunger is measured on a linear scale attached to the frame of the instrument. The rebound value depends on the surface hardness of the concrete and can be related to the compressive strength of the material. Procedure: 1. Observe the rebound hammer. Note the different angling positions and associated curves on the chart provided. 2. Grind and clean the concrete surface by rubbing with the abrasive stone that accompanies the rebound hammer. 3. Firmly hold the hammer in a position that allows the plunger to strike perpendicular to the testing surface. 4. Slowly increase the pressure in the plunger by pressing down until you hear the “click” and the hammer impacts. 5. Push the small button near the end of the rebound hammer to hold the reading. 6. Using the appropriate line on the chart, record the rebound number to two significant digits. 7. Press the hammer all the way down to release the small button, and slowly lift up the hammer. This step resets the readout. 8. Repeat Steps 1-7 and take 10 readings from each testing area. Record your numbers in the table below and find the average value. 9. NOTE: if one data point is not within 7 units of the average, dismiss that data point. If more than 2 points are not within 7 units of the average, the test must be redone. Calculations: Average the rebound numbers and compressive strengths for each test area. Results: Summarize your measurements and calculations in Table 3-2 below.
Page 17 Table 3-2: Rebound Data Location 1: Breezeway Floor (sound) Location 2: Breezeway Floor (cracked) Location 3: Garden Walls Angle of Attack: Angle of Attack: Angle of Attack: Trial # Rebound Number Compressive Strength Rebound Number Compressive Strength Rebound Number Compressive Strength 1 2 3 4 5 6 7 8 9 10 Avg. Notes:
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Page 18 Part II: Ultrasonic Pulse Velocity (UPV) testing (ASTM C597) Overview of Testing Apparatus: This test is used to assess the uniformity and quality of concrete. It can indicate the presence of voids and cracks and estimate the depth of cracks. The pulse generator/receiver has a timer that measures the elapsed time between initiation of a wave at the generating transducer and the receipt of the wave at the receiving transducer. This time together with the knowledge of the length of the sample allows for the calculation of the wave velocity. This wave velocity, along with the density of the specimen, can then be used to calculate the elastic modulus of the given sample. * Note: The testing device has been previously calibrated so that any signal transmission delay between the 2 cylindrical probes in neglected in all velocity measurements. Procedure: 1. Before testing, each specimen’s dimensions (length, width, height) will be recorded. 2. Make sure that the surface of the specimen is clean. 3. Turn on the UPV testing device and navigate to the “Test” menu. 4. Input the length of the specimen. 5. Apply a dime-size amount of grease to the two cylindrical receivers in order to make sure that the sound wave transmits correctly. 6. Place the first concrete specimen between the cylindrical probes so that the diameters of the probes are lined up exactly. Make sure that the setup is stable enough and the receivers do not tip over. 7. Under the test menu, scroll down to the second line, and press the ENTER. This will start the sound wave transmission. Students should be hearing 10 fast clicks; the sending probe is set up to send 10 signals per 1 seconds. 8. Let the clicks run for about 5-7 times, and record the highest number on the readout. This is the ultrasonic pulse velocity. 9. Once you obtain the velocity measurement, hit the CANCEL button to end the test. The machine should return to the Test Menu. 10. Carefully remove the concrete specimen from the probes, and check the probes to see if additional grease is needed. 11. Repeat Steps 1-8 for the other 4 specimens, and record the ultrasonic pulse velocity for each. Calculations: Calculate the average pulse velocity of each specimen using the equation: Length Time The relationship between the elastic modulus, E, and the calculated pulse velocity is given by the following equation: V
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Page 19 1  4 G  2  K  V 3 (1) Where K = material bulk modulus; K E 3 1 2 E (2) G = material shear modulus; G 2 1 (3) = material density (units consistent with units of K and G), and = Poisson’s ratio of the specimen Substituting Eqns. (2) and (3) into Eqn. (1) gives: V Results: - Summarize the specimen properties in Table 3-3. - Summarize the UPV results in Table 3-4. Table 3-3: Specimen Properties Sample Weight (lb) Length (in.) Width (in.) Height (in.) Diameter (in.) Volume (in. 3 ) Density (lb/in. 3 ) Porous OPC Asphalt E 1 1 2  1
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Page 20 Table 3-4: Ultrasonic Pulse Velocities and Stiffness Values of Specimens Specimen Velocity (ft/s) Elastic Modulus (psi) Plain Concrete Pervious Concrete Asphalt Notes:
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Page 21 Part III: Image Analysis using ImageJ Software Procedure: Scanning Procedure: 1. Connect the scanner to one laptop per group 2. Open Windows Fax and Scan 3. Place the sample in the middle of the scanner 4. Press “New Scan” 5. In the pop-up window, choose Document, Color, and set the resolution to 600. 6. Make sure to crop and prepare the pictures as neatly as possible Analysis using ImageJ for circular sections: 1. Open the image using ImageJ. File>>Open 2. Crop the image to a circular shape. First select a circular region (Elliptical selection tool while pressing shift key). Then go to Image>>Crop. The actual diameter of the circular section is 95 mm. 3. To specify the outer edges to remove, go to >>Edit>>Selection>>Specify. Enter the dimensions 900H×900W, ensure Oval is checked and hit OK. Reposition the circle to include more of the concrete. 4. Remove the outer edges using Edit>>Clear outside. 5. Resize the image to 570 pixels by >>Image>>Adjust>>Size (make sure to maintain the aspect ratio). 6. Select a 400x400 pixels section on the processed image. Rectangular selection>>Edit>>Selection>>Specify. Crop the selection. 7. Save the image in .jpg format for future use. 8. Now you may analyze the images. 9. Check whether the image is 8-bit by going to Image>>Type. If it is not an 8-bit image select 8-bit. 10. Crop any unwanted sections out if required (scale bar, empty spaces around sample, etc.) 11. Threshold the pores (Black phase) by >>Image>>Adjust>>Threshold>>Apply (in the window). 12. Note: ImageJ will analyze the areas of the image that have a value=0. To check which section this corresponds to (pore/solid or aggregate/paste), hover over one of the sections and note down the value shown on the Fiji Menubar. 13. Remove the noise in the image by going to Process>>Noise>>Despeckle. Repeat the process until you get a better image if required. You can also use the short keys (Ctrl+Shift+R). 14. Set the measurement data to analyze by going to Analyze>>Set measurements. Another window will pop up and check for area, shape descriptors, perimeter etc. Make sure to select “Limit to threshold”. 15. Analyze the image by going to Analyze>>Analyze Particles. Select Summarize.
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Page 22 Calculations: Using the Paste/Aggregate and Solids/Void fractions extracted from the ImageJ software, and the elastic modulus of the pervious concrete in Part II, calculate the Elastic Modulus of the solids using the following formula. Note that this applies for both OPC, Porous and Asphalt Concrete: E conc =E solids V solids E voids V voids Noting that the elastic modulus of air is zero and 𝑉 𝑠 olids + 𝑉 𝑣 oid 𝑠 = 1 . Then, using the elastic modulus of the solids, calculate the elastic modulus of the paste using: E solids E paste V paste + E agg V agg
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Page 23 Results: Tabulate the program pore results as shown Table 3-5: Table 3-5: ImageJ Results Slice No. of Pores (Count) Total Area Area Fraction Mean size E paste or E soilds (psi) Notes:
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Page 24 Group Discussion: 1. Is the rebound hammer test a legitimate way to determine the strength of in-place concrete? Justify. 2. Are the estimated compressive strength values within the acceptable range for concrete? 3. Which surface had the highest estimated compressive strength, which had the lowest, and is this what you expected to see? If not, why not? What could be some reasons for the discrepancy? 4. How do the UPV values for the different mix design specimens compare? Which sample had the highest UPV value, which one had the lowest, and based upon the relative air void content, do the UPV values make sense? 5. Are the calculated stiffness values within the acceptable range for concrete? If not, what could have caused the discrepancy? 6. Which sample had the highest stiffness and lowest stiffness, and how does this relate to the amount of air voids in the sample? 7. How did the pervious concrete specimens compare and why? Individual Discussion: 1. If the aggregate content was 10% more what would happen to the elastic modulus of the resultant concrete? 2. If porosity is increased/decreased to 30% what would happen to the elastic modulus of the resultant pervious concrete? Appendix Include any handwritten observations/drawings/calculations that you did during lab. Your actual typed-up calculations should go in the “Calculations” section.
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Page 24 Significance: In this lab, you will be measuring the viscosity of different liquids through different methods: rolling-bottle viscometer, Figure 4-1(a); sinking-ball viscometer, Figure 4-1(b); and a Zahn cup viscometer, Figure 4-1(c). The rolling-bottle viscometer is useful for liquids with low viscosities, the sinking-ball useful for high viscosity liquids, and the Zahn cup can be used with liquids from a range of viscosities by changing the specific design details of the cup. Different experimental techniques will be required to obtain accurate measurements of this widely varying property of liquids. Figure 4-1. Viscometers used in this lab; (a) rolling-ball viscometer, (b) Sinking- ball viscometer, and (c) Zahn cup viscometer. Apparatus: - Sinking-Ball Viscometer: Single steel ball o Asphalt cement - Zahn Cup Viscometer o Oil samples and paint Procedure: Before testing: 1. Understand what needs to be done before starting the test. 2. During testing, take note of the following (include in report): 3. Does the way the vial with the viscous liquid is being held against the back of the ramp affect the result? 4. What is the purpose of waiting while testing the viscous liquid? (c) (a) (b) LAB 4: VISCOSITY OF LIQUIDS
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Page 25 5. Are the tests accurate? 6. Why does the mass and volume of the liquids in the vials have to be consistent? Rolling-Ball: 1. Hold vial with one finger at the top of the ramp and release. 2. Recording the rolling distance. 3. Repeat 5 times for each liquid and take the average value. Precautions Handle the vials as little as possible to avoid warming the liquid. For the more viscous liquid wait about 3 minutes before running the test to assure temperature is ambient. Release vial by lifting finger straight up. (Do not push or restrict the vial in any way) Sinking-Ball 1. Record height of container and the diameter of the steel ball. (Adding the two will give the initial height) 2. Place steel ball in the center of the binder. 3. Record the height of the steel ball every 3 minutes. 4. Keep recording until the steel ball disappears from view. Precautions Once the ball is placed on the surface it cannot be removed. Stokes law assumes that the particle is sinking in a fluid of infinite extent so there are no wall effects as it sinks. Zahn-Cup 1. Record cup number being used and sample number being tested. 2. Dip cup into fluid until it is completely submerged. 3. Remove the cup from the fluid in a gentle vertical motion and start the timer. 4. Observe the fluid coming from the bottom of the cup and stop the timer at the first break in the fluid stream. Record this time as the efflux time for the sample. 5. When diluting the paint samples carefully weigh in the mass of water added and blend thoroughly. We will add water at 0% (non-diluted), 10%, 20%, and 40% by mass. After testing: 1. Assure tables are filled completely. 2. Review calculation section and understand equations. Calculations: For each specimen, show (with both symbols and numbers) how you calculated: Zahn Cup Zahn cup and similar viscometers utilize the correlation between flow and viscosity. The time that it takes a fluid to flow is dependent on the orifice that it must flow out of, the volume of material above the orifice (the head), and the viscosity of the fluid. This correlation is repeatable and well known even though the mathematics are highly complex. The cup type viscometers use the repeatable nature of the physical system and sidestep the
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Page 26 complex mathematics with relatively simple empirical expressions to relate the effluent time to the viscosity. Since the physical conditions suggest that the drain time is dependent on the orifice diameter a different equation is used for each cup type. The equations are below where t is the efflux time in seconds and h is the viscosity in Centistokes. Cup #1, 1 . 1 t 29 Cup #2, 3 . 5 t 14 Cup #3, 11 . 7 t 7 . 5 Cup #4, 14 . 8 t 5 Cup #5, 23 t Likewise there are some general guidelines for selection of the correct cup for a given fluid. In general the following guidelines are suggested: Cup #1, 18 cSt 56 cSt Cup #2, 40 cSt 230 cSt Cup #3, 150 cSt 790 cSt Cup #4, 220 cSt 1100 cSt Cup #5, 460 cSt 1725 cSt Combining the equations above with these ranges in viscosity tells us that the typical Zahn cup test should take approximately 20 seconds and 80 seconds. Tests taking less than 20 seconds should use a smaller numbered cup and tests taking longer than 80 seconds should use a higher numbered cup (unless you are already using a #5 cup). Blending Liquids The Refutas equation suggests that the viscosity of a blend of two viscous liquids is given by: VBN 10 . 975  exp exp Blend   0 . 8 blend 14 . 534  VBN Blend a VBN A b VBN B VBN i 14 . 534 ln ln i 0 . 8 10 . 975 Where; Results: exp VBN a,b = = = exponential function (e j ), Viscosity Blending Number, Mass proportion of liquid a and liquid b (e.g., if a blend consisted of 40% liquid = A and 60% liquid B then a = 0.4 and b = 0.6), and Kinematic viscosity of the liquids (cSt).
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Page 27 - Summarize your results in Tables 4.1 and 4.2. - Plot the penetration in the sinking-ball viscometer versus time. - Use the penetration versus time data with Stokes Law to estimate the viscosity of the asphalt cement. - Plot the viscosity versus water content for the paint from the Zahn cup viscometer. Table 4-1: Penetration Depth with Time from Sinking-Ball Viscometer. Time Scale Reading Table 4-2: Zahn Cup Times. Sample Type Zahn Cup Used Test Number Zahn Time (sec) Viscosity (cSt) Oil #1 1 2 3 Oil #2 1 2 3 Latex Paint Non- Diluted 1 2 3 Latex Paint + 10% water 1
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Page 28 2 3 Latex Paint + 20% water 1 2 3 Latex Paint + 40% water 1 2 3 Group Discussion: 1. Discuss the results from these tests. Address all of the following issues in this discussion: a. What is viscosity? b. Why is the sinking-ball viscometer so important looking at it from an applications perspective? c. What effect does temperature have on viscosity? d. Does the viscosity calculated from Stokes Law seem reasonable for the given binder (why or why not)? e. Discuss any limitations of the test and testing equipment. f. As always ELABORATE when answering questions in the discussion. 2. Compare your water-paint blended viscosities to the Refutas equation predicted results. Discuss any similarities or differences in both the magnitude of these comparisons and the trend with respect to water content. Individual Discussion: 1. The two oil samples are standard SAE motor oils. Using your results estimate which two standard grade oils were tested and explain how you made this conclusion. Cite at least two corroborating references for the standard viscosity of these oils.
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Page 30 LAB 5: FIBER-REINFORCED COMPOSITES AND CREEP OF POLYMERS Objective I. Understand the influence of fiber orientation on composite properties (E in this case) II. Be able to use principles of deflection of beams to calculate their properties III. Be able to set up, conduct and report experimental data in concise engineering terms Materials and Equipment 1. Fiber reinforced composite sheet from which 5 different beam pieces have been cut with differing fiber angles (beam size 7 in. long × 1 in. wide × 1/8 in. deep); 2. A simply supported set up with a span of 6 in. Span is changeable to understand the effects of span on deflection; 3. A dial gauge for deformation measurements; 4. Weights that are incremental by 250 g. Overview of Testing Materials Fiber-reinforced sheets are made up of fibers woven into a cloth mat orienting fibers into two orthogonal directions: the warp direction (lengthwise in the loom) and the woof direction (across the loom). When such a mat is used as a composite, the resulting mechanical properties are influenced by this orientation and are not isotropic. The purpose of this experiment is to measure the variation of the elastic modulus with respect to the orientation of the woven reinforcing mat in a composite. The second purpose is to demonstrate another technique for measure the elastic modulus of a material. The fiber reinforcement is glass and the matrix is a polyester polymer, with the fibers being placed as several layers of woven mats. The orientation of the specimens that were cut is shown in Appendix A. the object is to find the elastic modulus of each sample and determine how this modulus varies with the angle from the warp of the reinforcing mat. Note: The shading of the mat in Appendix A does not necessarily represent the orientation of the reinforcing fibers. Procedure 1. Examine the dial gauge; note its sensitivity and range. Note down the specimen number being tested. 2. Before you start measuring, make sure that the large hand is exactly on zero, and adjust it if necessary. Ensure there is good contact between the gauge head and the fiber-reinforced composite specimen and that it is located at mid-span. 3. Carefully stack the weights at mid-span in 250 g increments, up to 1250 g. Gently tap the dial indicator to ensure the needle is not stuck and read and record the deflection readings at each load increment. 4. Remove all the loads and repeat the above process twice (three readings in total) and calculate the average. 5. Move to the next station and repeat.
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Page 31 Calculations The mid-span deflection for a simply supported beam is well established. Consult engineering references to identify the appropriate equation for a simply supported beam subjected to a center point load. This equation can be rearranged to yield: E P f b , h Results Record the deformation measurements in Table 0-1 and Table 0-2 . Using the results in Table 0-1 and Table 0-2, plot the graph of load ( P ) as a function of deflection ( ), similar to the one shown below in Figure 0-1. Use the same axes for all five beams and label them appropriately. Use a linear regression to find the slope P/ of each plot (show on plot) and use it to calculate the Young’s Modulus of each beam, as outlined in the Calculations section. Express the Young’s Modulus in units of pounds per square inch. Finally prepare a plot of the Young’s modulus, on the ordinate, versus fiber direction, on the abscissa. Using the plot, develop a simple equation that relates E to the fiber direction. Figure 0-1: Load versus deflection plot 𝑃 Where = mid-span deflection, P = applied load; and ? = a function of the beam’s width (b) and height (h) [consult the references to determine
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Page 32 Table 0-1: Dial Gauge Readings Sample Weight (g) Dial Gauge Readings Deformation (in.) Set 1 Set 2 Set 3 Average 1 250 500 750 1000 1250 2 250 500 750 1000 1250 3 250 500 750 1000 1250 4 250 500 750 1000 1250
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Page 33 Table 0-2: Dial Gauge Readings (continued) Sample Weight (g) Dial Gauge Readings Deformation (in.) Set 1 Set 2 Set 3 Average 5 250 500 750 1000 1250 Table 0-3: Specimen Material Properties Specimen Fiber Orientation ( ° ) Young’s Modulus (psi) Group Discussion: 1. Which fiber orientation do expect displayed the largest/smallest deformation? Why do you think this is? 2. What is the relationship between fiber orientation and the materials Young’s Modulus? 3. What do your findings suggest about the structural applications of these fiber- reinforced composite materials? 4. List at least three items made of Composites; identify the Matrix and Reinforcement materials for each. 5. List a few advantages and disadvantages of using fiber-reinforced composites for structural applications. 6. Is there any discrepancy in your data? Do your graphs look like what you expected? If yes, explain why. If not, did you encounter any sources of error during the experiment? Explain. Individual Discussion: 1. Most composites are Pseudo-Isotropic, Orthotropic or Anisotropic; what do these three terms mean? 2. What is the primary function of the matrix in a composite material?
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Page 34 Appendix Any handwritten notes, such as observations during testing, dial gauge measurements, etc.
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Page 35 CREEP IN POLYMERS Objectives I. Explain the concept of creep and viscoelasticity using simple experimental tools II. Be able to predict the creep behavior of a polymer using simple equations for long term loading III. Understand the effects of molecular structure on long term deflections. IV. Understand the concept of fitting equations to describe observed physical phenomena Materials and Equipment - Samples with dimensions 12” long × 2” wide × 0.5” thick: a) Low molecular weight polyethylene b) High molecular weight polyethylene c) Polycarbonate d) Polystyrene e) Poly methyl methacrylate (PMMA) - Tip loads - Strain gauges - Data acquisition system that plots strains as a function of time The five different beams will be above or near their glass transition temperature at room temperature. However, their viscoelastic properties will be different owing to their different molecular structures and the fact that some of them are closer to their glass temperatures than others. Procedure A constant stress must be applied to the material to observe creep. A cantilever beam of each polymer will have a weight hung from its end, and the strain in the beam will be monitored as time passes. The loading situation is shown in Figure 0-1 below. The strain sensed by the gauge will be fed as an electrical signal to a recorder so that a plot of strain versus time will be obtained directly. Figure 0-1: Cantilever Beam Loading from side and end
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Page 30 Calculations: The stress at the gauge is given by: 2 Mh I = M P l = 3 12 bh I = The Burger’s model will be used to fit an equation for the creep curves obtained. A Burger’s model is shown below in Figure 2, where each of its mechanical elements has a constant associated with it. It should be noted that polymers are not actually made up of spring and dashpots, but it is merely a convenient way to visualize the various viscoelastic responses in order to derive an equation that describes them. Figure 0-2: Mechanical Representation of Burger's Model Burger’s equation for creep is: 2 2 1 1 2 1 1 1 E t t e E E = + +  𝜎 = stress 1. For each polymer, decide how many terms are required in the above equation based on the observed behavior. 2. Find the values of the constants in the equation, which will have units of a modulus or a viscosity. A BRIEF NOTE ON VISCOSITIES : Viscosity is defined as the ratio if sear stress to shear strain rate. In this experiment, normal stresses are applied and normal strain rates are measures, thus the viscosities calculated are not necessarily the same those measured in a classical shearing viscosity test (but are related). The viscosities in this experiment represent the “flow situation” and are the operant viscosities that allow the calculation of normal strains as a function of time where 1 2 where 𝜖 = strain and 𝜆 are model constants. A particular polymer may not exhibit all three fundamental responses (described by a separate term), in which case the term is simply dropped from the equation. The steps to fit the equation are as follows: ? = time 𝐸 , 𝜆 , 𝐸 1 2
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Page 31 when normal stresses are applied in the loading situation. Thus, the symbol 𝜆 is used to differentiate them from the true viscosity 𝜂 (which involves shear). The procedure for finding the values of these constants are based on the creep curve obtained from the experiment. A generalized version of the creep curve is shown below in Figure 0-3. Figure 0-3: Generalized Creep Curve 1. Section I of the curve is the instantaneous elastic response and is governed by the 𝐸 1 term, which is given by: E 1 = 2. Section III of the curve corresponds to the long-term viscous flow of the material and is associated with the 𝜆 1 , which is governed by the slope of the linear section III: 1 = 3. The extrapolation of the section III portion of the creep curve back till it intersects with zero time provides 𝜖 2 , which is the sum of both the instantaneous and delayed elastic strains. This, 𝜖 2 − 𝜖 1 represents the amount of delayed elastic strain and is governed by 𝐸 2 in the general equation, given by: 2 2 1 E = 4. The value 𝜆 2 controls the curvature of section II of the creep curve. It can be found by taking a data point within section II ( ? II , 𝜖 II ) and putting these into the overall equation with the previously calculated values of 𝐸 1 , 𝐸 2 and 𝜆 1 and solving for 𝜆 2 . It is best to do this along several points along the curved portion and using the average as 𝜆 2 . Section II Section I Section III Time
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Page 32 Perform a sanity check of your resulting equation by calculating several strains that should develop at several times during the first few minutes of loading. These calculated strains should be close to those that were actually measured. Use your equations to calculate the expected strain at the gauge if a 1 kg weight were hung on the beams for 1 month. Also, calculate the time that will be required for a 1 kg weight to generate a strain of 0.1 in/in (10%) at the gauge. Report these values in tabular form in your results. Include all calculations as part of the report! Results Of the five different beams, only the polystyrene and poly methyl methacrylate needs to be fit for an equation using the creep data using the calculations above. 1. Include a tabular summary of the constants for both polymers, with the moduli being reported as pounds per square inch (psi) and viscous constants in units of poise; 1 poise = 1 dyn · s/cm 2 . 2. Also include the strain v. time plots used for the calculations, adequately labeling the different sections and the corresponding model constants/variables on the plot (similar to Figure 0-3). Group Discussion: 1. Why are the materials “viscoelastic”? What is meant by this term? 2. Briefly talk about the various models used to represent viscoelastic materials and discuss their limitations. 3. Describe the three main stages of creep and what they represent. (Bonus: show a plot (strain as a function of time) representing the three main stages of creep with the stages adequately labeled). 4. How did the creep deformation of the five different beams differ? Which one demonstrated the most and least strain? 5. How did the strain v. time plot differ for each specimen? What does this tell you about their “spring and dashpot” behavior? 6. Understanding the relationship between instantaneous and delayed elastic response, how does the strain behave at prolonged periods? What do you think would happen after the load is removed? 7. How does temperature affect creep? 8. What are the real structural applications of creep? Individual Discussion: 1. Given that you have characterized a reference material with the Burger’s model. Examine the two scenarios below. Then identify and explain which model parameter will change and whether that parameter will increase or decrease. a. Under a fixed load, the instantaneous strain value is larger than that of the reference material. b. Under a fixed load, the instant strain value is the same as the reference material, but the rate of strain accumulation after 2 minutes is greater.
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Page 38
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Page 39 Significance: This test allows us to compare mechanical properties of various species and data for establishing strength functions. The test provides us with information about how the moisture content of wood influences the strength of wood in compression. Bending test on wood http://vimeo.com/1704966 (Note: This video is for bending test and you will be doing a compression test) Test Specimens: Table 0-1: Dimensions of Test Specimen Specimen Condition Average Initial Length (in. or mm) Average Initial Width (in. or mm) Average Initial Depth (in. or mm) Poplar Saturated Oven Dried Ambient Oak Saturated Oven Dried Ambient Apparatus: - Compression Testing Machine - Calipers and scale Procedure 1. Measure the length, width, and height of each specimen in 3 different places, and record the average values. 2. Measure the weight of each specimen and record the values. 3. Load the specimen vertically in the compression testing equipment so that the application of load is parallel to the direction of the grains. Additional Information : COMPRESSION TESTING OF WOOD Each group will receive 6 specimens: 1 saturated, 1 oven-dried and 1 ambient wood sample of both Poplar (Low Density Hardwood) and Oak (High Density Hardwood) wood species with the general dimension of 1.5”×1.5”×6”. Initial dimensions of samples subject to saturation or oven-drying will be provided by the TA. Summarize these values in the table below.
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Page 49 4. Apply load at a constant rate of 50lb/sec, or at a known constant rate that will run the test within a reasonable time (ASTM recommends a strain rate of 0.003 mm/mm (in/in)). 5. Continue loading the specimen until maximum load is reached, or if no peak is reached, until the load approaches a constant value. Observe when the specimen first starts to fail, and make note of any other observations during testing. 6. Stop the test. Remove the specimen from the machine and observe the failure type and direction of failure line. Calculations Calculate the stress and strain for each specimen (if you do not know how to calculate stress and strain review your statics and deformable solids notes). Calculate the moisture content of the saturated and ambient specimens using the equation: m m od 100 is the mass of the oven-dried wood. Results - Summarize the dimensions after testing in Table 0-2. - Summarize the sample dimensional properties in Table 0-3. - Summarize the characteristics of the test samples in Table 0-4 and Table 0-5. Table 0-2: Sample Dimensions After Testing Specimen Condition Average Final Length (in. or mm) Average Final Width (in. or mm) Average Final Depth (in. or mm) Poplar Saturated Oven Dried Ambient Oak Saturated Oven Dried Ambient where MC m od m od
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Page 41 Table 0-3: Sample Dimensional Properties Specimen Condition Change in Length (in. or mm) Change in Width (in. or mm) Change in Depth (in. or mm) Poplar Saturated Oven Dried Ambient Oak Saturated Oven Dried Ambient Table 0-4: Characteristics of Specimens in Compression Specimen Condition Volume (in. 3 or mm 3 ) Weight (kg or lb) Density (lb/in 3 or kg/m 3 ) Poplar Saturated Oven Dried Ambient Oak Saturated Oven Dried Ambient
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Page 42 Table 0-5: Characteristics of Specimens in Compression Specimen Condition Maximum Stress (psi or MPa) Maximum Strain Moisture Content (%) Failure Observations Poplar Saturated Oven Dried Ambient Oak Saturated Oven Dried Ambient Notes:
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Page 43 Group Discussion: 1. Note the type of timber used, and the rate of load application. Compare the six samples. Which samples displayed the most deformation (pictures or diagrams would be helpful)? Also describe how the dimensions of each specimen changed. 2. Is timber stronger when saturated, oven-dried or at ambient conditions? 3. Which type of timber was able to withstand the most applied pressure? How different were the failure strengths of each material? 4. How does the density of the timber affect its ability to withstand loads? 5. Which of the two materials was most affected by the saturation and drying process (compare with initial dimensions provided by the TA)? Why do you think this is? 6. Why is the moisture content of wood species important? Would the best wood to be used in outdoor structural purposes be the oven-dried wood? Why or why not? 7. What is meant by the Equilibrium Moisture Content (EMC)? Why is this important? 8. List a few advantages and disadvantages of drying timber for structural applications. 9. How do you think the timber would react if loaded perpendicular to the grain? Individual Discussion: 1. Explain what do your findings suggest about the nature and possible uses of each material?
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Page 44 Significance: In today’s lab, you will be performing many different experiments sieve analysis of a given mixture of aggregates, determining the dry rodded unit weight (DRUW) of a coarse aggregate, bulk specific gravity of a coarse and fine aggregate, moisture content of fine and coarse aggregate, and fine aggregate angularity. Sieve Analysis http://www.youtube.com/watch?v=-4qqqwzDWvI Coarse Aggregate Specific Gravity (at a minimum watch until 4:15) http://www.youtube.com/watch?v=O_Zi1U_IEaI&list=PLW9tOoRoXttcocpaa2WezVk _mbYcTSJqM Fine Aggregate Specific Gravity (at a minimum watch until 6:45) http://www.youtube.com/watch?v=D8YMIgW- 3UY&list=PLW9tOoRoXttcocpaa2WezVk_mbYcTSJqM Uncompacted Void Content http://www.youtube.com/watch?v=TJ7tOadgKyM PART I: Sieve Analysis (ASTM C136) Purpose: To determine the particle size distribution of an aggregate stockpile. Apparatus: - A mixture of fine and coarse aggregates that is at room temperature. - A stack of sieves arranged numerically from the pan (bottom container) to the top, as follows: Pan No.200 No.100 No.50 No.30 No.16 No.8 No. 4 3/8 in. 1/2 in. 3/4 in. - Mechanical sieve shakers that will help separate out the particle sizes. - Scales used to measure the mass of aggregate retained on each sieve. Procedure: 1. Measure the mass of the sample. This will be the original mass, M 0 . You will later compare this original mass to the cumulative mass after sieve analysis is done. 2. Check to make sure that the sieves are stacked in the correct order. 3. Carefully place the entire sample on the top sieve, and close the top sieve with a lid. 4. Place the stack of sieves into the sieve shaker, and agitate the sample for the time given by the TA. 5. Stop the sieve shaker, and carefully remove the stack of sieves, making sure that they stay in place. 6. Measure the mass of sample retained in each sieve. To do this, first place the empty container on the scale and tare it, then separately place the contents of each sieve into this container, and record the mass of each size increment. 7. Add up the masses retained on each sieve, and call this final mass M f (referred to as “Total” in the table). The final mass should be very close to M 0 . By convention, if the two amounts differ by more than 0.3%, the results cannot be accepted. (For the purposes of this lab we will ignore this requirement, but we will note it in the tables) 8. Re-stack the sieves in the correct order, making sure that they are “clean” enough for the next group to use. LAB 6 : AGGREGATES
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Page 45 Calculations: - Calculate the fineness modulus. - From your results, calculate the cumulative mass retained, the cumulative percent retained, and the percent passing for each sieve size (see sample Problem 5.3). Report all percentages to the precision specified in ASTM C136. In your report, under calculations, show one numerical example of how you obtained: cumulative mass retained, cumulative percent retained, and percent passing for a sieve size of your choice. Results: - Summarize the calculations for each sieve in Table 0-1 - Create a semi-log aggregate gradation chart just like the one on P. 499 of your textbook. Create the graph in Excel (or equivalent software) and make certain that you select a graph that correctly spaces the x-axis . - Create a 0.45-power chart like the one on P. 500 of your book (you may use the chart in Figure 0-1). Table 0-1: Results of Sieve Analysis Sieve Size Mass Retained (a), g Cumul. Mass Retained (b), g Cumul. Percent Retained (c) = (b)×100/Total Percent Passing (d)=100-(c) ¾ in. ½ in. 3/8 in. No. 4 No. 8 No. 16 No.30 No.50 No.100 No.200 Pan Total
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Figure 0-1: FHWA 0.45 Power Gradation Chart. Page 46
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Page 47 PART II: Specific Gravity and Absorption of Coarse Aggregate (ASTM C127) Purpose: To determine the mass-volume relationship quantities and water absorption potential of a coarse aggregate. Apparatus: - A sample of coarse aggregate that has been soaked (brought to 100% saturation) prior to lab. - Balance used to measure the dry mass, SSD mass, and submerged mass of the sample. - Wire basket used to immerse the coarse aggregate sample under water. - Towel/cloth used to quickly surface dry the sample. - Oven used to dry the sample so that the dry weight can be obtained. Procedure: 1. The coarse aggregate sample has already been soaked for 24+ hours prior to lab. 2. Take the tray out of the “water bath,” and try to remove as much water from the tray as you can. 3. Take the sample over to the wire basket, carefully dump the entire sample into the basket, and hang the basket from the scale so that the sample is submerged in the water. Record the scale reading as “C” this is the mass in water. 4. Carefully remove the wire basket from the tub, and dump all the aggregate onto the cloth/towel. Roll the sample in the towel until all visible films of water are removed. You do not have to “dry” the sample, just towel dry it enough to remove the moisture from the surface of the aggregate. 5. Record the mass of the sample after towel-drying, and call this “B” this is the saturated surface-dry mass. 6. Place the sample back into the original tray, and label the tray with your Group Name. Place the tray into the oven. The oven will be set at 110 ±5°C. Someone from your group will be responsible for coming back the next day and weighing the sample in order to get the oven-dry weight, “A.” Coordinate with your TA on the time that you will return Calculations: - Using the formulae from ASTM C127, show the numerical calculations for the following (don’t forget units on final answers and the required precision ): Bulk Specific Gravity (Equation 1) Bulk Specific Gravity (Saturated Surface Dry) (Equation 2) Apparent Specific Gravity (Equation 3) Absorption (%) (Equation 11) Results: - Use Table 0-2 and Table 0-3 to record the measurements Table 0-2: Coarse Aggregate Specific Gravity Measurements
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Page 48 Air Water Dry Mass Sample (A), g SSD Mass Sample (B), g Submerged Mass (C), g Table 0-3: Coarse Aggregate Specific Gravity Values Quantity Value Bulk Specific Gravity (OD) Bulk Specific Gravity (SSD) Apparent Specific Gravity Absorption % Notes:
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Page 49 PART III: Dry Rodded Unit Weight and Voids in Aggregate (ASTM C29) Purpose: To determine the dry compacted unit weight of a coarse aggregate stockpile. Apparatus: - Balance used to measure the mass of the sample - Tamping Rod - A cylindrical metal measure - Scoop for filling the measure with the aggregate Procedure: 1. Dry the aggregate sample to a constant mass, in an oven at 110 ± 5 ° C (This has already been done for you). 2. Fill the cylindrical measure one third full and level the surface with your fingers. 3. Rod the layer of aggregate with 25 strokes of the tamping rod evenly distributed over the surface. When rodding the first layer do not allow the rod to strike the bottom of the measure forcibly. 4. Fill the measure two-thirds full and again level and rod as above. When rodding this layer apply only enough force to cause the rod to penetrate to the first layer. 5. Finally fill the measure to overflowing and again rod as above. When rodding this layer apply enough force to cause the rod to penetrate to the second layer. 6. Level the surface of the aggregate with a straightedge in such a way that any slight projections of the larger pieces of the coarse aggregate approximately balance the larger voids in the surface below the top of the measure. 7. Determine the mass of the measure plus its contents and the mass of the measure alone. 8. Convert all of your masses to weights. Calculations: - Using the formulae from ASTM C29, show the numerical calculations for the following ( don’t forget units on final answers and the required precision ): Dry Rodded Unit Weight (DRUW) or bulk density (Equation 1) Voids % (Equation 4). Results: - Table 0-4 can be used to record the values you determine in the laboratory. Table 0-4: Dry Rodded Unit Weight and Voids Volume (ft 3 ) W measure (lb) W total (lb) DRUW (lb/ft 3 ) Voids (%) 0.25
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Page 50 PART IV: Specific Gravity and Absorption of Fine Aggregate (ASTM C128) Purpose: To determine the mass-volume relationships and water absorption potential of a fine aggregate. Apparatus: - Mold and Tamper. - Heat Gun to help us getting the sample to SSD. - Mason jar and pycnometer lid. - A balance or scale. - An oven Procedure: CONE TEST FOR SURFACE MOISTURE 1. Hold the mold on a firm non-absorbent surface. 2. Place a portion of the sample in the mold until overflowing. 3. Lightly tap the sample into the mold with 25 light taps of the tamper. 4. Lift the mold vertically, looking for the fine aggregate to slump slightly. TEST FOR SPECIFIC GRAVITY 1. The first step in this lab will be to calibrate the pycnometer. In order to do so, weigh the empty jar and then add water up to the calibration mark and weigh it again with the water. 2. Partially fill mason jar with water. 3. Weigh out 500 g ± 10g of SSD fine aggregate (Make sure to record the exact amount that you weighed). 4. Introduce the SSD fine aggregate into the mason jar and add more water to about 90% of jar capacity. 5. Place the lid and roll or agitate the mason jar to remove air bubbles for 5 min (be sure not to spill the contents of the jar). 6. Once full agitated add water to the calibrated mark. 7. Weight the mason jar with the fine aggregate and water up to the calibration mark. 8. Label a bowl with your group name and number. Remove fine aggregate from mason jar, place in your labeled bowl. 9. Place the sample in a oven at 110 ± 5 °C, and dry it to constant mass 10. Someone from your group will be responsible for coming back the next day and weighing the sample. Coordinate with your TA on the time that you will return. Calculations: - Using the formulae from ASTM C128, show the numerical calculations for the following (don’t forget the required precision ): Bulk Specific Gravity (Equation 1) Bulk Specific Gravity (Saturated Surface Dry) (Equation 3) Apparent Specific Gravity (Equation 5)
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Page 51 Absorption (%) (Equation 19) Results: - Table 0-5 and Table 0-6 can be used to record the values you determine in the laboratory. Table 0-5: Fine Aggregate Specific Gravity Measurements OD Specimen (A), g Pycnometer+Water (B), g Pycnometer+Sample+Water (C), g SSD Sample (S), g Table 0-6: Fine Aggregate Specific Gravity Values Quantity Value Bulk Specific Gravity (OD) Bulk Specific Gravity (SSD) Apparent Specific Gravity Absorption % Notes:
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Page 52 PART V: Moisture Content of Aggregate Stockpiles (ASTM C566) Purpose: To determine the amount of water held within an aggregate stockpile. Apparatus: - Balance - Oven - Sample container Procedure: 1. Determine the mass of the sample container and the weigh the aggregate sample. 2. Place the sample container in the oven until it is completely dry. 3. Someone from your group will be responsible for coming back the next day and weighing the sample in order to get the mass of the dried sample, after it has cooled. Calculations: - Calculate the moisture content using Equation 1 from ASTM C566. Results: - Use Table 0-7 to write your results. Table 0-7: Moisture Content Measurements Material Mass Container (g) Mass Sample (g) SP Mass Sample+ Container (g) OD Mass Sample+ Container (g) Moisture Content (%) Sand Coarse Aggregate Describe the Visual Condition of the Sand: Describe the Visual Condition of the Coarse Aggregate: Notes:
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Page 53 Figure 0-2: Fine Aggregate Angularity Test Apparatus PART VI: Uncompacted Void Content of Fine Aggregate (ASTM C1252) and Coarse Aggregate (AASHTO T 326) Purpose: To estimate the angularity of fine aggregate and coarse aggregate particles. Significance: This test method provides the void content of the fine aggregate and coarse aggregate which depends on the particle shape and texture. An increase in void content indicates a greater angularity or rougher surface texture. Apparatus: - Cylindrical Measure - Funnel - Funnel Stand - Glass Plate - Pan - Metal Spatula - Scale Procedure for determination of void content of fine aggregate 1. Weigh out the fine aggregate. 2. Position the jar and funnel in the stand and center of the cylindrical measure. 3. Use a finger to block the opening of the funnel and pour the test sample into the funnel. 4. Remove the finger and allow the sample to fall freely into the cylindrical measure. 5. After the funnel empties, strike off excess heaped fine aggregate from the cylindrical measure by a simple rapid pass of the spatula. 6. Try to avoid any vibration or any disturbance that can cause compaction of the fine aggregate. 7. Brush any grains from the outside and determine the mass of the cylindrical measure and contents. 8. Repeat the procedure for a second time. Procedure for determination of void content of coarse aggregate 1. Weigh out 5000 ± 10 g of coarse aggregate. 2. Center the cylindrical measure under the cylindrical hopper. Close and lock the gate of the hopper.
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Page 54 3. Use a finger to block the opening of the door and pour the aggregate sample into the funnel. 4. Remove the finger and allow the sample to fall freely into the cylindrical measure. 5. After the funnel empties, strike off excess heaped coarse aggregate from the cylindrical measure by a simple rapid pass of the spatula. 6. Try to avoid any vibration or any disturbance that can cause compaction of the coarse aggregate. 7. Remove any aggregate that fell outside the cylindrical measure and determine the mass of the cylindrical measure and its contents. 8. Retain all aggregate particles to perform the test for second time. Calculations: - Use the formulae from ASTM C1252 (Test Method A) and AASHTO T 326 to calculate the uncompacted voids in the materials. Results: - Use Table 0-8 to record the measurements from the test. Table 0-8: Uncompacted Voids for Fine Aggregate Sample Volume Container (V), mL Mass Sample (F), g Specific Gravity (G) Voids (U), % Aggregate 1 100 Aggregate 2 100 Glass Beads 1 100 Glass Beads 2 100 Table 0-9: Uncompacted Voids for Coarse Aggregate Sample Volume Container (V), mL Mass Sample (F), g Specific Gravity (G) Voids (U), % Aggregate 1 Aggregate 2 Figure 9-3: Angularity Test of Coarse Aggregates
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Page 55 Marble 1 Marble 2 Notes:
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Page 56 Group Discussion: 1. Using your gradation analysis and the stockpile definitions given in ASTM D448, determine the most likely aggregate stockpile that you sieved. 2. List and discuss three potential problems with a sieve analysis. How would each problem affect the test results? 3. In ASTM C128 and ASTM C127, what would be the consequences of failing to dry the aggregate to SSD before weighing it? Use a simple numerical example to prove your conclusion. 4. How is absorption of the aggregate related to the workability of concrete and to the amount of binder that is needed in an AC mix? 5. The method to find the specific gravity of coarse and fine aggregates is different, but both are based on the same basic physical phenomenon. What is this phenomenon? Explain the formulas used to calculate the fine and coarse specific gravities as well as the absorption. 6. Why is it important to calculate the specific gravity for both dry and SSD condition? Individual Discussion: 1. Look back at all of your calculated quantities (specific gravity, gradation, etc.) and assess their accuracy. Do any seem unusual? If so indicate which numbers are unusual. What are the expected range of values for the quantities measured, and why you think the numbers you obtained were right or wrong (experimental error, miscalculation, etc.). The answer to this problem will be unique to your team. Mis-identifying valid numbers as invalid will cost just as many points as not identifying questionable values . Even though this lab has 6 parts, you do NOT need to write four separate lab reports. Under “Apparatus and Procedure,” describe what each part of the lab entailed. You can put all your calculations under the same “Calculations” section (but be sure to clearly identify the calculations associated with each part).
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Page 57 In today’s four-part concrete lab, groups will create molds consisting of cement, aggregates, and water. The lab will consist of mixing a batch, performing a slump and air voids test, and preparing beams and cylinders to be used for further testing in lab the following two weeks. Prior to this lab you should watch the following videos: Mixing PCC http://www.youtube.com/watch?v=KNb0IbYrK8E Slump test https://www.youtube.com/watch?v=lwZf217v5XA Measuring yield test https://www.youtube.com/watch?v=2o9QFeDoIJU Measuring air voids of PCC air method https://www.youtube.com/watch?v=CfVaR79OgX8 Measuring air voids of PCC volume method https://www.youtube.com/watch?v=_Gq8PWmi7LQ Casting cylinders https://www.youtube.com/watch?v=TnEq-8I5Jn8 PART I Concrete Mixing (by weight) The lab class will be separated into 6 teams and 5 students for this lab. Each team will create a PCC mixture at a specific w/c ratio as shown in Table 0-1: Table 0-1: Water/Cement Ratio per Team Team Water/Cement Ratio 1 & 2 0.40 3 & 4 0.48 5 & 6 0.55 Since the aggregate is not at the saturated surface-dry (SSD) condition the aggregate will absorb water from the system (if it is in the air dried condition) or provide excess water to the system (if it is in the saturated surface wet condition) The w/c ratio is the weight of the free moisture above the absorption value divided by the weight of cement. Your TA should therefore provide you with the absorption of your aggregate and the moisture content of your aggregate. The amount of concrete you need to mix was calculated based upon the dimensions of the different molds and pressure meter you will be using: 1. 6 cylinders, 8” in height, and 4” in diameter 2. 1 beam, 4”x 4” x 18” 3. 1 cylinder, 12” in height, and 6”in diameter 4. 1 slump cone, (assumed to be a cylinder in order to stay conservative), 12” in height, and 6” in diameter (average) 5. 1 cylindrical pressure meter, 8.5” in height, and 8” in diameter LAB 7 : MIXING CONCRETE AND FRESH PCC PROPERTIES
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Page 58 The TA will provide you with the mix design for your team before the lab begins. Write this information down in Table 0-2. To develop these mix designs the TA used the properties shown in Table 0-3. Also, the amount of mixing water provided by the TA incorporates the water that will be absorbed by the aggregate. General Mixing Procedure: 1. Using a plastic bucket, scoops, and containers provided, measure out each ingredient on a scale. Make sure you zero the scale with the empty container on it, so that you are only weighing the materials, not the container also. 2. Wet the mixer and the wooden beam molds when used for the first time to avoid absorbing some of the mixing water. 3. Place the ingredients into the mixer in the following order: a. Fine aggregates (sand) b. Coarse aggregates c. Mix the coarse and fine aggregates for 1 minute d. Add 1 ½ lb of water e. Cement, in 2 equal increments. Continuously mix for about 30 seconds between each increment. f. Water, in 2 equal increments. Continuously mix for about 30 seconds between each increment. g. Mix the complete batch for an additional 5 minutes to ensure full distribution. Results: - Use Table 0-4 to record the actual batch weights for each team Table 0-2: Trial Batch Weights Material Trial Batch Wts. (lb) Teams 1 & 2 Teams 3 & 4 Teams 5 & 6 w/c Ratio 0.4 0.48 0.55 Cement Coarse Aggregate Fine Aggregate Water Table 0-3: Specific Gravity of Component Materials Material Dry Specific Gravity SSD Specific Gravity Water Content (%) Cement 3.15 N/A N/A
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Page 59 Coarse Aggregate Fine Aggregate Table 0-4: Actual Batch Weights Team Cement (lb) Coarse Aggregate (lb) Fine Aggregate (lb) Water (lb) 1 2 3 4 5 6 Notes:
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Page 60 Figure 0-1: Measuring the slump of freshly mixed PART II: Slump Test of Freshly Mixed Portland cement Concrete (ASTM C143) Purpose: To measure the slump of a freshly mixed PCC sample. Significance: The slump test is used to measure the consistency of freshly mixed PCC Apparatus: - Slump cone - Base - Tamping rod Procedure: 1. Place the base on the plastic sheet on the floor. 2. Place the slump cone on top of the base, and lock it in place. 3. Pour a 3” thick layer of concrete into the cone through the top opening. 4. Once poured, use the taming rod to agitate the sample 25 times 10 times in the center, and 15 times around the edges. 5. Pour a 4” thick layer of concrete into the cone. Agitate this layer 25 times also (10 times in the center and 15 times around the edges), making sure to reach into the underlying layer with the tamping rod. 6. Pour a 5” thick layer of concrete into the cone, so that there is a “hump” on the top of the cone. This hump will go down once you agitate the sample. Again, rod the topmost layer 25 times, making sure to reach into the underlying (second) layer, but not into the first layer. 7. After the top layer has been rodded, strike off the surface of concrete by screening and rolling the tamping rod across the top opening. 8. Release the clutches on the base, and lift up the cone vertically, without any horizontal or torsional motion. 9. Once the sample comes out, flip the cone upside down, and place it next to the sample, with the smaller opening on the bottom 10. Measure the slump by placing the tamping rod across the larger opening of the mold, and comparing the height of the sample to the height of the mold (see picture above). 11. Record the slump. 12. Repeat procedure 2 more times for a total of three replicates Results: - Use Table 0-5 to write down your results.
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Page 61 Table 0-5: Summary of Slump Test Results Team Trial Slump (in.) Team Trial Slump (in.) 1 1 2 1 2 2 3 3 3 1 4 1 2 2 3 3 5 1 6 1 2 2 3 3 Notes:
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Page 62 PART III: Air Content of Freshly Mixed Concrete by Pressure Method (ASTM C231) Purpose: To determine the air void content of freshly mixed PCC using an air meter. Significance: Air content is an important for the workability of freshly mixed concrete and for the strength and durability of hardened concrete. The air content of freshly mixed concrete is important for the proper proportioning of the mix. Apparatus: - Cylindrical volume measure - Balance or scale - Tamping rod used to agitate the samples - Mallet for striking side of container - Pressure meter Procedure: The operating instructions for the pressure meter are as follows: 1. Fill the base with a sample of fresh concrete, placing the concrete in the base by tamping. Place the concrete in three layers of approximately equal volume. Rod each layer 25 times uniformly. Rod the first layer throughout its depth. For each upper layer, allow the rod to penetrate through the layer being rodded and into the layer below approximately 1 in. After each layer is rodded, tap the sides of the bowl 10 to 15 times with a mallet to close any voids. Wipe the straight edge clean. 2. Weigh the container with the concrete sample, so you can calculate the unit weight of the concrete (TA will give you the volume of the measure). 3. Clamp on the cover with the petcocks open. 4. Using the rubber syringe, inject water through one petcock, while leaving the other petcock open. 5. Using the black built-in pump, pump up air to the “initial pressure” line on the dial gage. 6. Wait a few seconds for the compressed air to cool to normal temperature and then bleeding off, as needed. 7. Close both petcocks and press down on “thumb lever” to release the air into the base. Hold thumb lever down for a few seconds, lightly tapping the gauge with the finger to stabilize the hand on the dial. 8. DO NOT TILT THE METER AT ANY TIME. 9. Read the percent of air in concrete on dial. Record the air content below. 10. Open the petcocks to release the pressure and then remove the cover. Clean up the base, cover, and petcocks, using the hose. 11. Repeat this procedure one more time. Results: - Use Table 0-6 to write the results from each team.
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Page 63 Table 0-6: Summary of Unit Weight and Void Content Measurements Team Trial Volume of Measure (cf) Weight of Sample (lbs) Unit Weight (pcf) Air Content (%) 1 1 0.25 2 0.25 2 1 0.25 2 0.25 3 1 0.25 2 0.25 4 1 0.25 2 0.25 5 1 0.25 2 0.25 6 1 0.25 2 0.25 Notes:
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Page 64 PART IV: Making and Curing Concrete Cylinders and Beams (ASTM C31) Purpose: To determine how to make and cure concrete cylindrical and beam specimens. Significance: There are standardized requirements for making and curing Portland cement concrete specimens. The specimens will be used in next week’s lab to determine the strength and quality of the mix design. Apparatus: - Seven cylindrical plastic molds with covers (6 = 8” x 4”, 1 = 12” x 6” ) - One beam mold, with dimensions 4”x4”x18” - Tamping rod used to agitate the samples - Mallet for striking side of container - Concrete curing chamber in Concrete Lab Procedure: CYLINDERS: 1. Obtain two plastic cylinders for each sample you are to cast. 2. Coat the inside of each cylinder using a paper towel and the release agent. Be sure to thoroughly coat inside to promote release of the cylinder after initial cure. 3. Fill up the first-third of the cylinder with concrete. Using the tamping rod, rod the sample 25 times (10 times in the center and 15 times around the edges). 4. After the first layer has been rodded, tap the outside of the cylinder 10-15 times. 5. Add the second layer of concrete, so that the cylinder is 2/3 full. Use the tamping rod to agitate the sample 25 times as described above. Make sure that to “reach” into the first layer when rodding. Once done rodding, tap the outside of the cylinder 10-15 times. 6. Fill up the last third of the cylinder. Rod the sample again, making sure to “reach” into the second layer, but not the bottommost layer. Once done rodding, tap the outside of the cylinder 10-15 times. 7. Once done rodding and tapping, scrape off the top of the cylinder so that the sample has a smooth surface. 8. Do NOT cover the samples with the lid this will be done just before you leave the lab. 9. Let the samples sit for one day. Come back the day after lab, and place the samples in the curing chamber located in the concrete lab. Make sure to label the samples with each group’s number and lab day. 10. The cylinders will cure in a curing chamber for one week. Remove the samples from the curing chamber just before the following week’s lab. BEAMS: 1. Pick a beam mold. Groups with the same water content should share beam mold trays (i.e. Group 1 and 2 share a tray, Group 3 and 4 share a tray, and Group 5 and 6 share a tray). 2. Fill the beam mold with an even 2” layer of concrete. Using the tamping rod, rod the sample 60 times, making sure that you tamp the entire area evenly.
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Page 65 3. Fill the remaining 2 inches of the mold, and tamp the sample again 60 times. Make sure you “reach” into the underlying layer, but do not touch the very bottom of the mold. 4. Once done tamping, scrape off any excess concrete from the surface. Try to get the surface of the beam to be as smooth as possible. Do not cover the beam. 5. Let the beam sit for 1 day. Come back the day after lab and remove the sample from the mold. 6. Place the beam into the curing container, next to your group’s cylinder samples. Label your beam with your group number and lab day. 7. The beam will cure in water for 1 week. You will remove the samples from the curing medium just before the following week’s lab. Results: - Use Table 0-7 to summarizing the water-cement ratio, slump, unit weight, and air voids of the three different mixes: Table 0-7: Water Content, Slump, Unit Weight, and Air Voids of the Six Teams Team Actual Water- Cement Ratio Slump (in) Unit Weight (pcf) Air Voids (%) 1 2 3 4 5 6 Notes:
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Page 66 Group Discussion: 1. Go to ASTM C143, Section 9 and identify the allowable variability for the slump test. If each team represents a “Single - Operator”, which teams produced acceptable slump data and which teams produced unacceptable data? List three possible errors that could have occurred and explain if those errors would increase or decrease the measured slump. 2. Do you see any trends between water cement ratio and slump, unit weight, and air voids? How do these trends compare with your expectations? Be as specific as possible and include the amount of change you expect with changes in water cement ratio (it is insufficient to say you expect slump to increase/decrease with increases in water cement ratio, instead make sure you explain how much the value should change with the given water cement ratio changes). If expected trends are not met give three reasons why you think this occurred. Be sure to include example calculations in the appendix for any analysis that you perform. Individual Discussion: 1. Based on each team’s actual mixing results and what you know about the effects of water cement ratio on the strength and workability of PCC. Order the teams from 1 t o 3 based on which team you think will have the highest compressive strength. If you think more than one team will have the same (or approximately the same) strength then rank both equally. Explain your ranking.
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Page 67 In today’s lab, you will observe the behavior of last week’s concrete cylinders under a compressive load, and the behavior of the concrete beam under flexural testing. Prior to this lab you should watch the following videos to have a general idea about the nature of the different tests. The exact protocols followed in the lab may be slightly different than these videos. All of your writing should reflect what was actually done in the lab. In today’s lab, you will observe the behavior of concrete cylinders under a compressive load after 7 days of time in the curing room (depending on the semester schedule). Prior to this lab you should watch the following videos: Compression Test on Concrete https://www.youtube.com/watch?v=IR1U_bBiJic (fast forward to approximately 4:20 mark for testing. Prior to this is sample preparation, and we follow a different method) Splitting Tension Test http://www.youtube.com/watch?v=m bAeHLwvQ Flexural test on concrete https://www.youtube.com/watch?v=--ah--2R0wo&x-yt- cl=84924572&x-yt-ts=1422411861 PART I: Compressive Strength of Cylindrical Concrete Specimens (ASTM C39) Purpose: To measure the compressive strength of laboratory cast PCC samples. Significance: The compressive strength of concrete is a vital part of construction. It is a universal measure of the quality of the concrete mix. Apparatus: - A loading machine with two steel breaking blocks the upper block is spherically seated, and the bottom block is a solid surface. Test Specimens: - The specimens used will be the same specimens we molded in last week’s lab. The dimensions of all specimens are 4 inches in diameter, and 8 inches in height. LAB 8 : HARDENED PROPERTIES OF PCC
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Page 68 Procedure: 1. Using the digital caliper, measure the diameter of the two specimens in two different locations near the middle height of the specimen. Measure the diameter at a right- angle to the specimen. Report your values to the nearest 0.01 in (or to the nearest 0.25mm) and average them. This will be the “actual” diameter. 2. Put the breaking blocks on the machine into position. 3. Clean the surfaces of the breaking blocks and of the specimen. 4. Place a Neoprene cap on each side of the specimen. 5. Seat the specimen into the spherically-seated block, aligning the specimen’s axis with that of the block. 6. Apply a compressive load continuously (without shocks or breaks). The load we’ll be applying will be moving at 0.5% strain/minute. 7. Continue applying the load until the specimen breaks. During loading, observe the specimen for crack development, and once the test is finished, note the type of failure (failure angle, how long it took to fail, etc.). 8. Record the maximum load carried by the specimen during the test. Calculations: - Calculate the compressive strength of the PCC in pounds per square inch. Results: - Report the f c value of each specimen in tabular form ( follow precision specified in standard ). Also, record the maximum load it carried: Table 8-1: Properties of 7-day Old Concrete Cylinders Specimen ID# Max. Load (lbs) f c (psi) Failure Observations a Team Sample 1 1 2 3 2 1 2 3 3 1 2 3
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Page 69 4 1 2 3 5 1 2 3 6 1 2 3 a brittleness, surface texture, angle of breakage, level of crushing, time to fail, etc. PART II: Flexural Strength of Concrete (ASTM C78) Purpose: To measure the flexural strength of a laboratory cast PCC beam under four point (third point) loading conditions. Significance: Like the compression test, the flexural strength of concrete also indicates quality. Apparatus: - Loading machine that is capable of delivering loads at a constant rate. Force must be applied perpendicular to the face of the specimen and applied without any eccentricity. Test Specimens: - The specimen used will be the beam molded in last week’s lab. Its dimensions are 4” by 4” by 18”. Procedure: 1. Mark each specimen 1 in. from each side and then divide the span of the beam L by 3. Mark each section as shown in Figure 8-1.
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Page 70 2. Turn the test specimen on its side so that it is positioned exactly as it was molded, and center it on the bearing blocks. 3. Center the loading apparatus with respect to the applied force. Bring the load-applying blocks in contact with the surface of the specimen at the third points between the supports. 4. If there exists a gap in excess of 25 mm (0.004 in.) between the load-applying blocks , the supports, and the specimen, grind or cap the contact surfaces of the specimen, or shim with leather strips. 5. Apply the load rapidly up to about 50% of the breaking load. Then, apply the load continuously at a rate that constantly increases the extreme fiber stress between 125psi and 175 psi (860kPa and 1210kPa) per minute. The rate we’re using is 0.05 in/minute. Continue loading until rupture occurs. Calculations: - Calculate the modulus of rupture using either Equation 2 or Equation 3 in ASTM C78. Follow precision requirements. If the fracture occurs outside of the acceptable range for ASTM C78 make a note of this and use Equation 3. Results: - Summarize your findings in Table 8-2 and Table 8-3: Table 8-2: Dimensions of Flexural Test Specimen Team Average width (in.) Average depth (in.) Span length (in.) Line of Fracture Location a 1 2 3 6. Measure the dimensions of the specimen to the nearest 0.05in (1.3mm) using the digital caliper. Take three measurements across each dimension, and average these to find the average width, average depth, and average length. Locate the line of fracture location at the section of fracture and record your findings in the table below.
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Page 71 4 5 6 a middle third, outside the middle third but acceptable, outside middle third and unacceptable Table 8-3: Properties of Concrete Beam used in Flexural Bending Test Team Maximum applied load (lb) Modulus of rupture (psi) Existing defects in specimen prior to testing 1 2 3 4 5 6 a surface voids, pre-existing cracks, uneven surface, etc.
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Page 72 PART III: Splitting Tensile Strength of Cylindrical Concrete Specimens (ASTM C496) Purpose: To measure the splitting tensile strength (Brazilian Test strength) of a laboratory cast PCC sample. Significance: The splitting tensile strength of PCC is another indicator of the tensile properties of PCC and is also used to design structural lightweight concrete members. Apparatus: - Testing Machine - Supplementary Bearing Bar or Plate Procedure: 1. Draw diametric lines on each end of the specimen using a suitable device that will ensure that they are in the same axial plane. 2. Determine the diameter of the specimen by averaging three diameters measured near the ends and the middle of the specimen. 3. Determine the length of the specimen by averaging at least two length measurements taken in the plane containing the lines marked on the two ends. 4. Center one of the strips along the center of the lower-bearing block. Then, place the specimen on the strip and align so that the lines marked on the ends of the specimen are vertical and centered over the strip. 5. Place the second strip lengthwise on the cylinder, centered on the lines marked on the ends of the cylinder. Make sure that the projection of the two lines marked intersects the center of the upper bearing plate. 6. Apply the load continuously at a constant rate within the range of 100 to 200 psi/min splitting tensile stress until failure. 7. Record the maximum load applied. Calculations: - In order to calculate the splitting tensile strength of your specimen refer to Equation 1 from the ASTM C496 standard. Results: - Use Table 8-4 and write the results from each team.
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Page 73 Table 8-4: Splitting Tensile Strength of Concrete Team Diameter (in.) Max Load (lb) Splitting Tensile Strength (psi) 1 2 3 4 5 6 PART IV: Ultrasonic Pulse Velocity Group Discussion: 1. Give typical values for the 7 day compressive strength of PCC. Cite your reference for these values and provide a second reference that confirms this range of values. Then comment on your 7 day strength tests with respect to these values. Are they higher, lower, approximately the same, etc. Also, comment on your overall trends with respect to water/cement ratio and the trends that are typically reported, e.g., are your results the same or different and how are they different from those typically observed. If differences in either the compressive strength or trends with water/cement ratio are observed speculate as to why these differences occurred. 2. List and discuss the sequence of events that led up to the failure of a concrete cylinder in direct compression. Explain why a tensile failure in PCC is very rapid and brittle in comparison. 3. Suppose that an overnight rainstorm increased the % total moisture content for all aggregates by 2.5 percentage above those that were used in the mix you made (e.g. if the water content for the aggregates in your mix was 1% then the new water content would be 3.5%). What effect could this change have in terms of strength and workability if you weighed in the same amount of aggregate, free water, and cement? Quantify these effects as much as possible. For example it is insufficient to simply say that the strength would increase/decrease you should discuss how much of increase or decrease you would expect. 4. Compare the UPV elastic modulus with the elastic modulus determined by ASTM C469. 5. Compare the lab results for compression and elastic modulus at 7 days and compression, splitting tension, and modulus of rupture at 14/21 days to the ACI *For the Ultrasonic Pulse Velocity refer to Lab 3 Part II*
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Page 74 predictions that are shown below. Use the average f c values for these calculations. Create a summary table with the measured and predicted values from each team. Estimate the error of the predictions based on the equation shown in the table below. Discuss how well these equations predicted the measurements. Quantity Relationship Error Modulus of Rupture f r 7 . 5 f c Error Measured Predicted 100 Measured Splitting Tension f ct 6 f c Elastic Modulus E 57 , 000 f c 6. The most general form of Abram’s law for portland cement concrete is summarized below. a. Determine the values of coefficients A and B for both the 7 day and 14/21 day strengths. b. Assuming a linear relationship between these coefficients and time, estimate the values of A and B for the 28 day case and predict the 28 day compressive strength of your PCC. c. Compare your predictions to the rule of thumb that is typically used to estimate the 28 day compressive strength from the 7 day strength. d. Discuss three reasons why these two predictions do or do not match well. A f c B w / c Individual Discussion: 1. In this lab we have tried to examine the effects of water cement ratio on PCC strength, modulus, workability, and void content. Suppose you are in charge of a lab that is responsible for developing a very high strength concrete for use by a small Southeast Asian country. Devise a study to comprehensively evaluate the effects of air void content on the engineering behavior of PCC for structural application. Include in this study the specific experiments that are necessary, appropriate standard specification designations, necessary replicates, mixing conditions, air void levels to study, component materials to include, etc. Include all the details necessary for a technician to take your document and carry out the study. In a separate section of your answer include a list of any information that you cannot readily assume, but that would need to be found out before embarking on this study. You may type your answer to this discussion question, but your answer should be unique. Copying another person’s answer or replicating another person’s answer in a close way will result in penalties to both parties.
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Page 75 PART I: Viscosity Determination of Asphalt Using a Rotational Viscometer (ASTM D4402) Purpose: To determine the rotational viscosity of asphalt cement binder at elevated temperatures. Significance: Asphalt viscosity is important for quality control and quality assurance. It allows proper handling of asphalt and is used to find the mixing and compaction temperatures of asphalt concrete. Apparatus: - Rotational viscometer. - Spindles (No. 27). - Thermosel system. Procedure: 1. Initial setup including powering the Thermosel and initial temperature equilibrium has already been performed by your TA. 2. Remove the sample holder with the test specimen from the oven. 3. Place the loaded chamber back into the thermo-container using the extracting tool. 4. Lower the viscometer and align the thermo-container. 5. Insert the spindle into the liquid in the chamber and couple it to the viscometer. 6. Allow the asphalt to come to the equilibrium temperature (about 15minutes). 7. Start the viscometer at 20rpm. 8. Record three readings, taken at 60-second intervals, at each test temperature in the table below. Calculations: - Average the three viscosity readings taken at each test temperature. Results: - Record your measurements in Table 0-1. - Plot your data on the viscosity chart shown in Figure 0-1. Table 0-1: Viscometer Readings for Asphalt Binder Test Temperature (°C) Viscometer Reading 1 Viscometer Reading 2 Viscometer Reading 3 Average Viscometer Reading (cP) 135 LAB 9 : ASPHALT CEMENT TESTING AND GYRATORY COMPACTION
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Page 76 160
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Figure 0-1. Temperature-Viscosity chart for identifying mixing and compaction temperatures.
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Page 78 PART II: Penetration Test of Asphalt Binder (ASTM D5) Purpose: To measure the penetration of an unknown asphalt cement binder at two different temperatures. Prior to the lab watch https://www.youtube.com/watch?v=HQH5Wf07tRk Significance: The penetration test is used to measure binder consistency. A higher penetration value indicates a softer consistency. Apparatus: - Penetration apparatus and needle (Each increment on the dial gage is equal to 1/10 mm), sample container of binder, water bath, transfer dish, thermometer Procedure: 1. Clean and dry the needle with a clean cloth, and insert it into the penetrometer. For room temperature of 25 ° C, place a 50-gram mass on top of the needle, so that the total moving load comes to 100 grams. For 4 ° C, place the 50-gram and the 100-gram mass on top of the needle, so that the total moving load comes to 200 grams. 2. Place the sample container in a transfer dish, and transport the specimen over to the penetrometer. The transfer dish is vital to keeping the temperature of the sample constant. 3. Place the transfer dish on the stage of the penetrometer. 4. Using the large dial, adjust the moving head of the penetrometer so that the needle is positioned close to the surface of the binder. Using the smaller controller right above the needle, make fine adjustments to the needle. Position the needle so that it just barely touches the surface of the binder. 5. Move the top black handle down so that the “gap” between the two measuring rods is closed. This is the “base” position. 6. Mark the base reading in the table below, under “start.” 7. With the metallic button in the “up” position, press the red button. The timer will start, and the needle will penetrate the sample for 5 seconds. 8. Again, move the top black handle down so that the gap is closed. This is the “end” position. 9. Mark the dial gage reading from the “end” position in the table below. The difference between the “end” and the “base” reading is the penetration value (or pen value). 10. Repeat Steps 1-11 in three different positions throughout the surface of the binder. 11. Each member from the team will perform this test at 25 °C and only one per team at 4°C. Calculations: - Using the following formula to calculate the viscosity, in centipoises Results: - State the average penetration value for each of the two test temperatures in Table 0-2 and Table 0-3. - Use Table 0-4 to summarize the average penetration values from each team.
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Page 79 Table 0-2: Penetration Values at 4 ° C Temp. 4°C Group 1 4°C Group 2 Trial # 1 2 3 4 5 6 Start End Difference Start End Difference Start End Difference Average Table 0-3: Penetration Values at 25 ° C Trial Measure S1 S 2 S 3 S 4 S 5 S 6 Average 1 Start End Diff. 2 Start End Diff. 3 Start
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Page 80 End Diff. Table 0-4: Penetration Values from All Teams Group Team Machine 4 ° C Penetration (avg.) 4 ° C Viscosity (avg.), cP 25 ° C Penetration (avg.) 25 ° C Viscosity (avg.), cP 1 1 2 3 2 4 5 6 Notes:
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Page 81 PART III: Dynamic Shear Modulus of Asphalt Cement (ASTM D7175) Purpose: To determine the dynamic shear modulus, |G*|, and phase angle, , of an unknown asphalt cement binder. Significance: The Dynamic Shear Rheometer is an important apparatus in characterizing asphalt cement binder. The dynamic shear modulus is an indicator of the stiffness or resistance of asphalt binder to deformation under load. The dynamic modulus and phase angle define the resistance to shear deformation of the asphalt binder in the linear viscoelastic range. The linearity test sets the linear viscoelastic limits. Apparatus: - A Dynamic Shear Rheometer Procedure: SHEAR MODULUS 1. Place the 25 mm upper and lower plates. 2. Set the gap as follow: a. Observe the upper and lower plate measuring contact by rotating the upper plate and slowly lowering the tube with the knob on the right hand side of the DSR until the plate stops rotating b. Raise or lower the vernier scale ring so that when the tube is bottomed out against the scale collar, the plates are just touching. This is ZERO gap position c. Adjust the gauge to read zero by rotating the zero with the indicator, then tighten the Allen screw d. Raise the upper plate using the position adjustment knob on the right to allow clearance for setting the gap e. Rotate the micrometer stop adjustment knob turning it counterclockwise to the desired gap (1.05 mm for the 25 mm plates) 3. Loading the sample: a. Place the sample in the center of the bottom plate b. Lower the upper plate onto the sample, slowly squeezing the sample between the plates until you reach the stop setting (1.05 mm) c. Trim the excess material with the trimming tool 4. Once the sample is trimmed, remove the extra 50 microns from the gap turning the stop adjustment knob clockwise 50 microns. Turn the right position adjustment knob counterclockwise to lower the upper plate to this setting 5. Place the plastic cover and let the water run at test temperature. LINEARITY TEST 1. After shear modulus test is done. Change the test mode to Linearity Test on the DSR Software. 2. The test will start running at a 2% strain and be increased in 2% increments up to 30%. Record all shear modulus (G*) for each strain level. You should have a total of 15 readings.
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Page 82 Results: - Use Table 0-5 to write down the results from all groups. - In Table 0-6 record the readings for the linearity test. - Your TA will send you data for the other tests needed to determine the asphalt binder grade. Table 0-5: DSR Test Results Team Aging Level Temperature (°C) |G*| (Pa) Phase Angle (degree) 1 2 3 4 5 6 Table 0-6: Linearity Test Results Strain (%) Shear Modulus |G*| (Pa) Strain (%) Shear Modulus |G*| (Pa) Strain (%) Shear Modulus |G*| (Pa) 2 12 22 4 14 24 6 16 26 8 18 28 10 20 30 Notes:
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Page 83 PART IV: Gyratory Compaction (ASTM D6925) Purpose: To demonstrate the use and functionality of the Superpave gyratory compactor. Watch the following video https://www.youtube.com/watch?v=2xpfiqF1kiw Significance: The device is used for the Superpave volumetric mix design of asphalt concrete mixes and for field quality control during the construction of HMA pavements. The gyratory compactor is used to create samples that will ultimately be used to determine the asphalt content and aggregate gradation for asphalt concrete mixtures. Different trial specimens, with different aggregate gradations and asphalt contents are prepared, and they are compacted using the gyratory compactor. For Superpave requirements the internal angle of gyration is 1.16 degrees, the compaction rate is 30 gyrations per minute, and the vertical pressure is 600 kPa (87 psi). The number of gyrations used to achieve different levels of compaction is as follows: - N ini the number of gyrations represents the initial compaction level that helps identify “tender” mixes. Such mixes lack stability during construction, and they tend to displace rather than compact under loads. - N des the number of gyrations necessary to achieve a level of compaction that represents the compaction level just after the end of the construction process. - N max the anticipated compaction level that is achieved at the end of the pavement’s lifetime. Depending on the projected number of equivalent single axle loads (ESALs) the pavement is going to experience, the number of gyrations varies. For light traffic, with ESALS of less than 0.3 million applications of load, the maximum number of gyrations (N max ) is 75, whereas for heavy traffic, with ESALs exceeding 30 million applications of load, the maximum number of gyrations is up to 205. You can find a summary table of this information in Table 9.9 on page 367 of your book. Apparatus: - Superpave Gyratory Compactor Sample Preparation: Each group will make 2 replicates of their mix design. The asphalt content for each mix will vary; some will have 5.0, 5.5 and 6% asphalt content by weight. The materials used in this mix design have the properties summarized in Table 0-7. The mix design will be given by your TA. You can write your mix design in Table 0-8. For this exercise we will be designing the asphalt mixture for a traffic level of 2 million EASAL ( N ini = 7, N des = 75, N max = 115 ). Table 0-7: Material Specific Gravities Material Specific Gravity Asphalt Cement 1.030 Coarse Aggregate Fine Aggregate
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Page 84 Table 0-8: Asphalt Mixture Design for each Team Team Coarse Aggregate (g) Fine Aggregate (g) Asphalt (g) 1 2 3 4 5 6 Procedure: MIXING ASPHALT CONCRETE 1. Weigh out the appropriate amounts of the required aggregate size fractions and combine in a bowl to the proper batch weight. Typically, a batch weight of 4500 - 4700 grams of aggregate will provide enough material for a finished specimen height of 115 ± 5 mm, if the combined aggregate specific gravity is between 2.55 - 2.70. 2. Heat the binder and the combined aggregate in an oven to the appropriate mixing temperature for the binder to be used. This ensures that the binder is fluid enough to coat the aggregate particles. 3. Place the heated aggregate in the mixing bowl and thoroughly dry mix the sample. Make a crater in the center of the aggregate in the bowl and weigh in the required amount of binder. Begin mixing immediately. A mechanical mixer may be used. 4. Determine the proper compaction temperature range for the binder used. 5. After mixing, spread the loose mixture in a flat, shallow pan and short term condition the mixture as detailed in AASHTO R 30. 6. Place the compaction mold and base plate in an oven to preheat to the required compaction temperature. 7. Bring the mixture to the proper compaction temperature, by placing it in another oven at the compaction temperature (normally there would be an aging step, but we will omit this process for this lab). 8. Once compaction temperature is reached proceed with compaction. GYRATORY COMPACTION OF ASPHALT CONCRETE 1. Verify all settings for angle, pressure and number of gyrations. 2. Verify the height recording device is turned on and is reading in the proper units. 3. When the compaction temperature has been reached, remove the mold and base plate from the oven. Put the base plate in position in the mold and place a paper disk in the bottom of the mold. 4. Charge the mixture into the mold in one lift. A funnel or other device may be used to place the mixture into the mold. Take care to avoid segregating the mix in the mold,
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Page 85 but work quickly so that the mixture does not cool excessively during loading. Level the mix in the mold and place a paper disk on top. 5. Place the mold in the gyratory. 6. Press mold lower and once the mold is lowered press mold lock to secure the mold and then press start. 7. The gyratory will stop automatically when the specified number of gyrations has been reached. 8. Remove the mold from the compactor and extrude the specimen from the mold. Take care not to distort the specimen when removing the specimen from the mold. A cooling period of 5 to 10 minutes may be necessary with some mixtures; a fan may help speed the cooling process. Remove the paper disks while the specimen is still warm to avoid excessive sticking. Calculations: - Estimate the G mb of each compacted sample by using the measured height and assuming a smooth walled cylinder. Results: - Summarize the results from each compaction in Table 0-9. - Summarize the actual asphalt contents that were blended in the laboratory in Table 0-10 (you will use the actual asphalt contents in Lab 13). Table 0-9: Compaction Results for Each Team Team Sample Height (mm) Bulk Specific Gravity ( Estimated ) @ N ini @ N des @ N max @ N ini @ N des @ N max 1 1 2 2 1 2 3 1 2 4 1 2 5 1 2 6 1
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Page 86 Table 0-10: Actual Asphalt Content for Each Sample Team Target Asphalt Mass (g) Actual Asphalt Mass (g) 1 2 3 4 5 6 Notes: 2
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Page 87 Group Discussion: 1. Estimate the proper mixing and compaction temperatures for your binder. Then, discuss three consequences that might occur during the mixing and compaction process if your thermosel was mis-calibrated so that the actual temperature of the sample was 5 ° above the recorded temperature. 2. Determine the strain limit for your asphalt binder at the test temperature where you performed the test. Use a threshold error of 90% of the |G*| value at 2% strain in this determination. Include in this answer a logarithmic plot of |G*| versus strain level and a vertical line indicating where you determined the limit to exist (include sample calculations in the appendix to support this strain level). Based on this plot, what would be the consequence on the asphalt binder grade if the |G*|/sin( ) test was performed at too high of a strain level. 3. For the 25 ° C penetration tests, evaluate each member of your team and determine who performed the penetration test with an acceptable level of repeatability. For 4 ° C penetration results assess your team’s results for acceptability. Show your assessment and discuss the results (refer to ASTM D5 for appropriate thresholds). 4. For both the 25 ° C and 4 ° C penetration tests use the average values from each team to assess the within laboratory and between laboratory precision. Treat all teams in a group as a single laboratory and the two groups as two separate laboratories. Discuss the results (threshold values can be found in ASTM D5). 5. Briefly summarize the general procedure for preparing, placing, and compacting samples using the gyratory compactor. What criteria are considered choosing the materials and when putting together the mix design? Individual Discussion: 1. Determine the standard PG grade of your asphalt binder. Show all the steps you took in determining this grade.
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Page 88 PART I: Theoretical Maximum Specific Gravity of Hot Mix Asphalt (ASTM D2041) Purpose: To determine the maximum theoretical specific gravity of an asphalt concrete mixture. Significance: Theoretical Maximum Specific Gravity (G mm ) is used to calculate the percent of air voids in a compacted HMA. The values for G mm will depend on the mix design and the aggregates used. Air void content is an important indicator of the quality of an asphalt concrete mixture. Due to the time requirements we will only be performing two of these tests per group. Apparatus: - Vacuum Container - Balance - Vacuum Pump - Mechanical Shaker Procedure: 1. The first step is to weigh the container with water (D). 2. Separate the particles of the HMA sample by hand, taking care to avoid fracturing the aggregate. 3. Place sample into the container and determine the mass and designate the net mass of the sample as A. 4. Add enough water to cover the sample completely. 5. Remove air trapped in the sample by applying gradually increased vacuum for 15 minutes. Make sure to agitate the container and contents using the mechanical shaker. 6. After vacuum, fill up the container with water, close the cap and weigh the container filled with water and the mix sample (E). Calculations: - Using the formulae from AASHTO T209, show the numerical calculations for the maximum specific gravity (don’t forget the required precision ). Results: - Summarize your results in Table 0-1 LAB 1 0 : ASPHALT CONCRETE TESTING
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Page 89 Table 0-1: Maximum Specific Gravity Test Team Mass Sample (OD) (A), g Mass Container+ Water (D), g Mass Container+ Water+Sample (E), g Maximum Specific Gravity 1 2 3 4 5 6 Notes:
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Page 90 PART II: Bulk Specific Gravity of Compacted Bituminous Mixtures (ASTM D2726) Purpose: To determine the bulk specific gravity of an asphalt concrete sample. Significance: The outcome of the Bulk Specific Gravity of Compacted Bituminous Material’s test is used in the void analysis of the compacted asphalt mix. The air void content of an asphalt concrete mixture is an important indicator of quality. Test Specimens: Students will be using the specimens that were compacted during the Preparation of Asphalt Concrete Specimens Using the Gyratory Compactor lab. Fill in Table 0-2 Table 0-2: G mm values Asphalt Content (%) Maximum Specific Gravity Apparatus: - A balance suitable for suspending specimens into a water bath and measuring the submerged weight. Procedure: 1. Weigh the specimen in air, and record the mass as A. 2. Immerse the specimen in water that is at 25±1°C (77±2°F) while it is suspended from the balance for 3 to 5 minutes. Record the immersed mass as C. 3. Remove the specimen from the water bath, and surface dry it by blotting with a damp cloth. Weigh the specimen, and record the surface-dry mass as B. Calculations: - Using the formulae from ASTM D2726, show the numerical calculations for the bulk specific gravity and water absorption (don’t forget the required precision ). Designate the specific gravity determined by these equations as G mb ( measured )@ N max
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Page 91 - Compare your measured G mb to the G mb calculated for N max from your previous lab (see Table 13-9) and calculate the correction factor, C. G mb measured @ N max C G mb estimated @ N max - Use the correction factor to calculate the G mb (c orrected ) for each sample from Lab 12 at N ini and N des (assume C is constant for both samples of a given team). G mb corrected C G mb estimated - Use the G mm in Table 0-2 and the G mb ( corrected )@N des to compute the air void content at N des . P 1 G mb corrected @ N des 100 a G mm - Average and report the air void content for each compacted asphalt concrete sample. - For each sample, calculate %G mm @N ini , %G mm @N des , %G mm @N max , VMA @ N des and VFA @ N des G mb corrected % G mm G mm 100 VMA 100 % G mm @ N design G mm R s G sb VFA ( VMA P a ) VMA 100 In the VMA equation you will need to calculate the G sb of your fine and coarse aggregate blend (G sb values were given in the previous lab). The R s variable represents the proportion of aggregate in the mix; M coarse M fine R s M M M coarse fine asphalt Results: - Report the bulk specific gravity (G mb ) value and the water absorption (%) at N des ., Table 0-3. - Report the correction values for each team in Table 0-4 - Report G mb ( Corrected ), %G mm @N ini , %G mm @N des, and %G mm @N max for each team in Table 0-5. - Report the air void content, VMA, and VFA at N des in Table 0-6
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Page 92 - Create a plot of air void content versus asphalt content using all 12 of the lab samples and identify the asphalt content that should yield an air void content of 4%. - Create similar plots for VMA and VFA at N des and indicate whether the mix design meets the required specifications (your TA will inform you about the type of mixture you are working with so that you can identify these specifications). Table 0-3: Density Results for Each Team Team Sample Mass Sample (A), g Saturated Surface Dry Mass (B), g Immersed Mass (C), g Bulk Specific Gravity @ N max Water Absorption (%) 1 1 2 1 3 1 4 1 5 1 6 1 Table 0-4: Summary of Correction Values for Each Team Team Sample C 1 1 2 1 3 1 4 1 5 1 6 1 Bulk Specific Gravity ( Measured )@N max Bulk Specific Gravity ( Estimated )@N max
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Page 93 Table 0-5: Corrected Bulk Specific Gravity and %G mm Team Sample Bulk Specific Gravity ( Corrected ) %Gmm @ N ini @ N des @ N max @ N ini @ N des @ N max 1 1 2 2 1 2 3 1 2 4 1 2 5 1 2 6 1 2
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Page 94 Table 0-6: Volumetric Properties of Sample Specimens at N des Team Sample Air Void Content @ N des (%) VMA @ N des VFA @ N des 1 1 2 2 1 2 3 1 2 4 1 2 5 1 2 6 1 2 Notes:
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Page 95 PART III: Mechanical Test Purpose: To evaluate the moisture susceptibility of an asphalt concrete mixture. Significance: The significance of this test is evaluating the sensitivity of a given material to the negative effects of moisture, which can erode the bond between aggregate and asphalt and negatively impact the long-term performance of the material. Specimens, Apparatus, and Procedure: Your TA will explain and show you the basic procedure for the indirect tension test. You will combine your testing efforts with another team to learn about the impacts of moisture damage in asphalt concrete. One of the samples that you compacted last week has been cut into two test specimens prior to the lab. Also prior to the lab one of the test specimens has been saturated with water via vacuum saturation and then left overnight in a 60 ° C water bath. Depending on the material and the void structure, this water may react with the asphalt cement to degrade the adhesive bond between the aggregate and asphalt (we refer to this as stripping since it visually appears that the asphalt has been stripped away from the aggregate surface). If severe enough the strength of the sample can be negatively affected and you will visually see evidence of the moisture damage. Approximately 2.5 hours before the lab this water bath was cooled to the testing temperature of approximately 25C. The second specimen was also submerged in the same water bath (although protected from the water) to ensure that both specimens were at the same test temperature. The indirect tension test is an incredibly popular test for asphalt concrete for three essential reasons; 1) it is relatively quick to do, 2) it provides an indication of the tensile properties of the sample, and 3) the sample geometry involves a thin asphalt concrete disk that can be easily obtained from in-service pavements, which are built-up in lifts of approximately 1-3 inch layers of asphalt. The test is very similar to the splitting tension test that we say in portland cement concrete, except we use a thin sample. When loaded along the diametrical axis the sample experiences compressive stress in the vertical direction and a mostly uniform tensile stress in the horizontal direction. You may not be able to visualize that there is tensile stress in the horizontal direction, but think about how the splitting tension test failed, it was a vertical crack, driven by the horizontal tensile stresses. Calculations: - Observe and record the peak force from the computer screen. - Calculate the tensile strength by using the following formula (be aware of units!): S t 2 P t d S t = Tensile strength (psi),
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Page 96 P = Maximum load (lbf), t d = = Thickness of the specimen (in.), and Diameter of the specimen (in.). - Compile the tensile strength for both the non-moisture conditioned sample and the moisture conditioned sample and calculate the tensile strength ratio (TSR), defined as: TSR S t Moisture Conditioned S t Dry - Visually observe the failure surface and comment on whether you see any visual evidence of stripping. Table 0-7: Air Void Content for Each Sample at N des Sample Peak Load (lbf) Maximum Stress (psi) TSR Comments Moisture Conditioned Non-Moisture Conditioned Notes:
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Page 97 Group Discussion: 1. Use the heights of your samples to estimate the bulk specific gravity of all the compacted samples at N ini , N des , and N max (assume a smooth walled cylinder for this purpose). a. Average the replicate tests and summarize the results in a table. b. Explain whether the true G mb should be larger or smaller than your estimate. c. Discuss your expectations with respect to specific gravity and asphalt content. If the measured data do not support this expectation provide three possible reasons why. d. Will the following changes likely increase, decrease, or have no effect on the density of a compacted asphalt concrete sample; 1) using coarse aggregate with a higher density, 2) using coarse and fine aggregates with greater angularity, and 3) using aggregates with greater absorption. 2. Most agencies consider an acceptable mixture one that exhibits a TSR value above 0.8. Does your mixture meet this criterion? 3. Speculate on what would happen to the dry tensile strength if the test were performed at a higher temperature. Would you expect an increase or decrease in tensile strength as the temperature increased? Individual Discussion: 1. Explain why you cannot compare the TSR results from the teams that tested other asphalt contents to accurately assess the impacts of asphalt content on moisture damage susceptibility. Then design a group of experiments that would let you identify the effect of increasing asphalt content on moisture susceptibility. This experimental design should be clear enough that a technician working in the laboratory would have enough details to conduct your experiment. Hint: Technicians and TA’s like tables that neatly summarize everything (identify the asphalt contents, air void contents, test rates, replicates, and all other necessary information).
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