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Feb 20, 2024
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Title: Buffer Preparations
Results
Weak acid, Strong acid, Weak base, and Strong base are combined to create buffer
solutions with a pH of 7.00. A given pKa of phosphate buffer is 7.2. Potassium phosphate
(K
2
HPO
4
174 g/mol) is the weak base, and potassium phosphate, monobasic (KH
2
PO
4
136
g/mol), as the weak acid. NaOH was the strong base. and HCl was the strong acid. Table 1
represents the buffer preparation calculation when acids and bases are paired in order to get the
mass. Table 2 reviews results of the pH for each of the buffer types and their average pH. The
ingredients were measured out with a target pH of 7.0, a volume of 50 mL, and a concentration
of 0.1M using the Henderson-Hasselbach equation. Table 3-4 represents the calculated pH and
the buffer capacity calculations.
Table 1 Buffer preparation for process 1-3
Method 1 (WA+WB)
Method 2 (WB +SA)
Method 3 (WA+SB)
Mass of KH2PO4
(g)
0.4216 g
XXXXXXXXXXX
0.68g
Mass of K2HPO4
(g)
0.330 g
0.871g
XXXXXXXXXXXX
Volume of 1 M HCI
(mL)
XXXXXXXXXXXX
3.1 mL
XXXXXXXXXXXX
Volume of 1 M
NaOH (mL)
XXXXXXXXXXXX
XXXXXXXXXXXX
1.9mL
Volume of H2O
(mL)
50 mL
46.9 mL
48.1 mL
Final Volume (mL)
50
50
50
For Table 1 Henderson-Hasselbach equation was used for method 2 and 3. Stoichiometry allows
the calculation of Method 1. The calculations were used with the pH given of 7.0, a volume of
50mL and 0.1M concentration.
Calculations
HA = H2PO4 = 136 g/mol
A-= HPO4^2 = 174 g/mol
7.0= 7.21 + log10 ([A-] / [HA] ) = -0.21 = log10([ A-] / [HA] )
([A-] / [HA] ) = 10^-0.21= 0.616
Method 1:
Final volume x concentration x nw = mass
0.616 [HA] + [A-] = 0.1 m :
1.616[HA]= 0.1 m
[HA] 0.1m / 0.616=
0.062
M
[A-] = 0.616 m x 0.062m =
0.038
M
Now ,
[HA]= 50 / 1000 L x 0.062m x 136g/ mol =
0.4216
g
[A-] = 50/1000 L x 0.038 m x 174 g/ mol =
0.330
g
Method 2
Equation: C1V1= C2V2
[A-1] : V1= 0.062m x 50 mL =
3.1 mL
[ HA] : V1 = 0.038 m x 50 mL =
1.9 mL
Method 3
mass = volume x concentration x nw
[A-] = 50 / 1000 mL x 0.1m x 136 g/ Mol =
0.68 g
[HA] = 50/1000 mL x 0.1m x 174g/mol =
0.87 g
Table 2: Ph measurements of buffers
Buffer
Measured Ph
Method 1 (WA+WB)
6.49
Method 2 (WB +SA)
6.58
Method 3 (WA+SB)
6.6
Average
6.56
Table 3 Buffer Capacity
Calculated pKa was measured by subtracting the literature pKa minus the pH given then subtract
the average pH in Table 2.
Literature Pka - ( pH given - average pH )
7.21 -( 7.0- 6.56 ) =6.77
Buffer
Starting Ph
Measured Ph after
addition
Calculated Ph
Buffer + 0.5 mL
HCI
6.58
6.51
6.77
Buffer + 0.5 mL
NaOH
6.6
6.9
6.77
Water + 50
μL HCI
7.58
3.02
6.77
Water + 50
μL
NaOH
7.58
10.86
6.77
Table 4: Buffer Capacity Calculation
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The initial calculation was determined by using the initial values in Method 1.
[HA] = ( 50/ 1000 L x 0.062 x 1000) = 3.1
[A-] = (50 /1000 L x 0.038 m x 1000 ) = 1.9
The change in mmol was determined by the equation below.
10^-6 x 500 microliters x 1 mol/ L x 1000 mmol = 0.5 mmol.
The end mmol was determined by subtracting the change from the initial values.
The above equations were used to determine the values of buffer solutions. However the same
process was used for unbuffered calculations, but instead of using 500 microliters, use 50. %0
microliters were added to the capacity experiment.
HA
Weak Acid (
buffered)
A-
Weak base (
buffered )
HA
Weak Acid (
unbuffered)
A-
Weak base (
unbuffered )
Initial mmol
3.1
1.9
3.05
1.85
Change in mmol
0.5
0.5
0.05
0.05
End mmol
2.6
1.4
2.55
1.35
Discussion
The purpose of the buffer lab was to prepare and measure the pH of three buffer types.
The calculations were found using the henderson-hasselbalch equation. Stoichiometry was used
for the solid potassium phosphate dibasic and monobasic, however amounts were added to a
liquid volume since it is solid. The liquid ingredients HCI and NaOH were massed using the
calculation form of C1V1= C2V2. During the lab, grams and milliliters were used to calculate
each buffer. Experimental errors could have occurred when calculating or rounding certain digits
before the final calculations. However, there was a minor error in the process when calculating
the mass amounts at the beginning of the lab.
When calculating the buffer capacity the henderson-hasselbalch equation was used again
to measure the three acids and the two acids with the pH closest to each other were chosen.
During the experiment HCI was added to one of the chosen and the other chosen acid was added
to NaOH then measured the pH for each new buffer. Buffer capacity calculations
The pK2 was calculated by using the assigned pH of 7.0 and subtracting the average pH,
then the literature pKa of 7.21 was subtracted. Example, ( 7.21- (7.0- 6.56)). The pH values
obtained were all less than the assigned pH given. This means that my prediction at the
beginning of the lab was satisfied. However, there might have been errors when conducting my
experiment such as errors with liquid transfer, solid massing errors or pH meter reading errors.
The experiment was designed and established to understand acid and base concentrations
and the usage of henderson-hasselbalch equation. The provided beakers were measured to be 50
mL. The solution volume was also 50 mL. This can cause accidents of spilling or splashing when
stirring or transferring the products between the cylinder and the beaker. It would be beneficial to
have larger beakers to hold the buffer solution.
Questions:
1.
Your goal is to make 100 ml of 0.1 M buffer at a pH of 4.7 using method #2. You are
given sodium acetate, HCl (1 M), The sodium salt of bicarbonate - NaHCO3 (salt of the
weak acid), and Sodium carbonate - Na2CO3 (its conjugate base). Determine which of
these four you will need and then show the calculations including the pKa value of the
chosen buffer.
The concentration of acid and salt should be the same. The concentration of sodium acetate =
0.05 acetic acid. The volume given is 100 mL, Moles = 0.005 moles. Take 0.005 mL of the 50
mL sodium acetate and react it with 50 mL of 0.05M HCl.
2.
2. You are given sodium acetate, HCl (1 M), NaHCO3, and Na2CO3. Determine which
of these four you will need and then show the calculations(include the pKa of the chosen
buffer) to make a buffer of pH 9.9 using method #2. Assume you are making 100 ml of a
0.1 M buffer.
Equation used: pH=pKa+log ([salt])/([acid])
9.9=10.1+log ([Na2CO3])/([NaHCO3]) —>
([Na2CO3])/([NaHCO3]) =0.63
[Na2CO3]+{NaHCO3]=0.1M
0.63[NaHCO3]+[NaHCO3]=0.1—-> [NaHCO3]= 0.0613M
Moles=Molarity x Volume=
0.0613 x 100/1000=0.00613 moles
[Na2CO3]=0.1-0.613=0.938 M or moles=0.0938
3.
3. By consulting a buffer table of pKa values, suggest a buffer system other than
phosphate or carbonate and calculate the raGo of the conjugate base/acid concentrations
to obtain a buffer at pH 6.6.
pH = pKa + log [base]/[acid] —> 6.6 = 6.49 + log [base]/[acid] → log [base]/ [acid] = 6.6-6.49
[ A- ]/[0.5 M ] =1.29 -> 0.65 M
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>
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