Carloa Andres Palacios_Química General - copia

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Anexo 2 Tarea 3 - Disoluciones y gases Tablas para el desarrollo de los ejercicios. Nombre y apellidos: Código (documento de identidad) Nombre del tutor: Programa académico: Ingeniería Industrial Ejercicio 1. Leyes de los gases ideales Tabla 1. Leyes de los gases ideales Número de estudiant e Ley de Boyle Ley de Charles Ley de Gay-Lussac 5 Un gas ocupa un volumen de V1 a una presión de P1. Si la temperatura permanece constante, ¿Cuál es la presión en mm de Hg, si se pasa a un recipiente de 3 litros? V 1 =1,5 L P 1 =5,50 torr 5,50 torr x 760 mmHg 1 torr = 4180 mmHg P 1 x V 1 = P 2 x V 2 Una llanta de un vehículo se llena con (V1) de aire a T1. Luego de rodar varios kilómetros la temperatura sube a (T2) ¿Cuánto será el volumen de aire (V2) en la llanta? V 1 = 23 L T 1 = 32°F T 2 = 74°F V 1 x T 2 = V 2 x T 1 V 2 = V 1 xT 2 T 1 Un gas se encuentra a una presión P 1 y una T 1 ¿Cuál será la presión si la temperatura se incrementa a T 2 ? P 1 =1,52 atm T 1 =35°C + 273,15 = 308,15K T 2 = 221 K P 1 x T 2 = P 2 x T 1 P 2 = P 1 xT 2 T 1

Número de estudiant e Ley de Boyle Ley de Charles Ley de Gay-Lussac P 2 = P 1 xV 1 V 2 P 2 = 4180 mmHg x 1,5 L 3 L P 2 = 2090 mmHg ( ° F − 32) × 5 9 = ° C T 1 = ( 32 − 32) × 5 9 = 0° C T 1 = 273K T 2 = ( 74 − 32) × 5 9 =23,33° C T 2 = 23,33° C + 273,15 T 2 = 296,48K V 2 = 23 L x 296,48 K 273,15 K V 2 = 25L P 2 = 1,52 atm x 221 K 308,15 K P 2 = 1,090 atm

Ejercicio 2: Gases ideales Tabla 2. Gases ideales Número de estudiant e Gases ideales 3 Una cantidad X 1 de gas ideal ocupa un volumen V 1 a una temperatura T 1 y, una presión P 1 que se debe calcular a partir de la ecuación de gases ideales. I. ¿Cuál es la presión que se requiere para comprimir ½ volumen del gas (V 2 ) contenedor a 200 °C? X 1 = 85,5 Kg NO x 1000 g 1 K g = 85500 g NO 85500 g NO x 1 mol NO 30 gNO = 2850 mol NO V 1 = 2,5 L T 1 = 82°C + 273,15 = 355,15 K T = 200°C + 273,15 = 473,15 K PV = nRT

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P 1 = nRT V P 1 = 2850 mol NO x 0,08205 at x L K x mol − g x 355,15 K 2,5 L P 1 =33219,66 at Para calcular la nueva presión P 2 del gas, debemos utilizar la ley de Boyle-Mariotte, que establece que la presión de un gas ideal es inversamente proporcional al volumen ocupado cuando la temperatura y la cantidad de sustancia se mantienen constantes P 1 x V 1 = P 2 x V 2 P 2 = P 1 xV 1 V 2 P 2 = 33219,66 at x 2,5 L 1,25 L P 2 = 66439,32 at II. Si se va a encerrar en un tanque de Volumen V 2 (correspondiente al punto I), el cual puede resistir una presión manométrica máxima de 6 atm, ¿cuál sería la máxima temperatura del gas si se desea que el tanque no estalle? PV = nRT Tmáx = PV nR

Tmáx = 6 atm x 1,25 L 2850 mol NO x 0,08205 at x L Kxmolg Tmáx = 0,032 K Ejercicio 3: Soluciones. Tabla 3. Soluciones Númer o de estudia nte Datos del ejercicio I II III 5 Estudiante 3: Se desea preparar 60 mL 0,5 N de una solución de HCl, a partir de un frasco almacén del ácido que se encuentra al 37% y cuya densidad es de 1,18 g/mL. I. ¿A qué concentración molar se encuentra el frasco almacén de ácido? II. ¿Cuál es Se desea preparar 60 mL 0,5 N de una solución de HCl, a partir de un frasco almacén del ácido que se encuentra al 37% y cuya densidad es de 1,18 g/mL. I. ¿A qué concentración molar se encuentra el frasco almacén de ácido? Eq g soluto = N x litro de solución 60 mL x 1 L 1000 mL = 0,06 ¿Cuál es el porcentaje peso a peso de la concentración molar final? Eq g soluto = N x litro de solución 60 mL x 1 L 1000 mL = 0,06 L Eq g soluto = 0,5 N x 0,06L Eq g soluto = 0,03 III. ¿Cuál es la fracción molar de soluto presente en la solución final? Xmolar = molessoluto molestotales 0,40 gHCl x 1 mol HCl 36,45 g = 0,0 Xmolar = 0,0109 mol 0,0109 moles Xmolar = 1

el porcentaje peso a peso de la concentración molar final? III. ¿Cuál es la fracción molar de soluto presente en la solución final? L Eq g soluto = 0,5 N x 0,06L Eq g soluto = 0,03 0,03 eq g HClx 36,45 g mol HCl 1 eq − g HCl ¿ 1,09 g mol HCl Masa HCl = 1,09 g HClx 37% /100 Masa HCl = 0,40 g HCl d = m V V = m d V = 0,40 gHCl 1,18 g / mL V = 0,3417 mL x 1 L 1000 mL = 0,0 0,03 eq g HClx 36,45 g mol HCl 1 eq − g HCl ¿ 1,09 g mol HCl % p p = masasoluto masasolución x 100% d = m V m = d xV m = 1,18 g / mL x 0,3417 mL m = 0,40 g % p p = 0,40 g 0,40 g x 100% % p p = 100%

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m = 0,40 g HClx 1 mol HCl 36,45 g = 0 M = moles desoluto litrosde solución M = 0,0109 mol HCl 0,000341 L M = 32,05 Ejercicio 4: Aplicación del tema Tabla 4. Aplicación del tema asignado Número de estudiante 3 Área de campo asignada Zootecnia Title In vitro fermentation characteristics of ruminant diets using ethanol extract of brown propolis as a nutritional additive Abstract The addition of levels of ethanol extract of brown propolis was evaluated by assessing diet degradation in rumen fluid and predicting cumulative in vitro gas production by nonlinear (dual pool logistic and exponential) models. A total of 35 g of crude propolis were extracted in 65 mL of cereal alcohol (95% ethanol). In a completely randomized factorial design, the experimental diets combined four concentrations of extracted propolis diluted in cereal alcohol (0, 50, 70, and 100% of propolis extract) and supplementation doses (4, 8, 12, 16, and 20 mL/kg dry matter), tested in triplicate. Diet

(400 g/kg Tifton hay and 600 g/kg concentrate) was incubated for 96 h carried out three times in three different weeks. There was significant interaction between extract concentration and dose on the dry matter (DM) degradability. Dry matter degradability of diet decreased exponentially as a function of the increase in dose (y = 678.55×dose –0.271 ). Pure alcohol treatment showed a negative exponential effect, with degradability of 303.61 g/kg when administered at a dose of 20 mL/kg DM. Treatment 100% ethanol extract reached the greatest degradability, estimated at 18.93 mL/kg DM. The treatment with 70% extract showed 6.35 mL/kg DM and the 50% extract, 7.65 mL/kg DM of minimum degradability. The reduction potential of pure ethanol was –0.32 mL gas/mL. Estimates of maximum gas production by dual pool logistic and exponential models were 13.10 mL and 12.07 mL for 100% extract, respectively. The 100% extract produced the highest gas production estimates, above 30 mL gas/100 mg DM of fermented diet. The degradation and fermentation of ruminant diet can be improved using 13 mL/DM kg of ethanol extract of propolis. feed additive; gas production; propolis; ruminal degradability; ruminant nutrition Introduction Propolis is a natural product with antimicrobial activity ( Park et al., 2000 ; Stradiotti Júnior et al., 2004b ). The chemical composition of propolis is quite complex and diversified because it depends on the ecology of plants visited by bees that produce it ( Ghisalberti, 1979 ). Several studies have demonstrated that the antimicrobial activity of propolis occurs by the inhibition of bacteria classified as Gram-positive ( Ghisalberti, 1979 ; Bankova et al., 2000 ; Vargas et al., 2004 ). However, the effects of dilution

according to the type of propolis still have to be elucidated to obtain solutions with sufficient active principle to obtain such effects on the rumen microbiota. According to Mirzoeva et al. (1997) , propolis and some of its components, such as caffeic acid phenethyl ester and quercetin, are bacteriostatic to Gram-positive and some Gram-negative bacteria, inhibiting their motility, likely because they modify the bionergenic status of bacterial membranes. This action is similar to that of ionophores, which are commonly included in ruminant diet because of their conditioning role in the ruminal environment, capable of improving the utilization of metabolic energy and decreasing lactate levels and protein deamination ( Prado et al., 2010 ). Like ionophores, propolis has been used as an additive in ruminant nutrition to inhibit the production of gases, particularly methane, and to decrease nitrogen losses during ruminal fermentation ( Stradiotti Júnior et al, 2001 ; Stradiotti Júnior et al., 2004a ; Ítavo et al., 2011 ; Heimbach et al., 2014 ). Silva et al. (2014) studied the effects of dietary brown propolis on nutrient intake and digestibility in feedlot lambs compared with monensin and concluded that the addition of brown propolis has the same effect as monensin, with neither of them maximizing nutrient availability in diets for feedlot lambs at seven months of age. According to Makkar (2005) , in vitro gas production has been considered a suitable method to assess the action of phytochemicals on ruminal microbial fermentation. Groot et al. (1996) reported that different nonlinear models with specific assumptions and parameters are available to fit curves of cumulative in vitro gas production, allowing degradation parameters to be determined and increasing understanding of fermentation

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kinetics. The present study tested the addition of different concentrations and doses of brown propolis extract to ruminant diet and evaluated the effects of this supplementation on diet degradation in rumen fluid, in addition to assessing the kinetics of cumulative in vitro gas production through exponential ( Ørskov and McDonald, 1979 ) and dual pool logistic ( Schofield et al., 1994 ) nonlinear models. Discussion Ethanol propolis extract showed contents of wax (29.90 mg/mL), dry residue (151.28 mg/mL), total phenols (27.65 mg/mL), and total flavonoids (13.98 mg/mL) above the quality parameters established by Brazilian law (IN.3, Brasil, 2001 ), which determines minimum levels of 0.25% flavonoids (2.5 mg/mL) and 0.50% phenolic compounds (5.0 mg/mL). Dry matter degradability decreased exponentially as a function of the increase in doce.Thus, including increasing doses of pure ethanol in the rumen fluid has a negative effect on microbial activity and substrate fermentation by anaerobic microorganisms in the rumen fluid. Likewise, the negative control also decreased cumulative in vitro gas production, yielding 6.9 and 7.9 mL/100 mg DM according to the dual pool logistic and exponential models, respectively. The use of 100% extract resulted in the highest in vitro degradability, which suggests that components in the propolis extract promoted increasing degradation of diet DM in the rumen fluid, likely through the selection and stimulation of certain rumen bacteria,

especially the Gram-negative variety. The antimicrobial action of propolis on bacterial growth, membrane potential, and motility was studied by Mirzoeva et al. (1997) . They found that propolis affects the permeability of the bacterial inner membrane to ions and causes dissipation of membrane potential, hindering ATP synthesis, ion transport, and motility of Gram-positive bacteria. The antibacterial activity of propolis against Gram-positive bacteria is strong but limited against Gram-negative bacteria ( Bankova et al., 1999 ; Marcucci et al., 2001 ; Packer and Luz, 2007 ). Although the cell walls of Gram-negative bacteria are less rigid than those of their Gram-positive counterparts, their higher resistance to propolis likely results from the higher complexity of these structures, with liposaccharides and high lipid content ( Vargas et al., 2004 ). The flavonoids contained in the propolis extract act against microorganisms through inhibition of cell membrane function, bacterial activity, or synthesis of nucleic acid ( Cushnie and Lamb, 2005 ). This explains the higher degradability and cumulative gas production of diets, added with propolis extract in relation to the negative control, which had complete bactericidal action. The treatment with 70 and 50% extract showed minimum degradability estimates close to 7 mL/kg DM (6.35 and 7.65 mL/kg DM, respectively). These similar estimates indicates that even after extract dilution in 30 or 50% water, microbial fermentation and gas production are still affected. The results suggest that the content of 13.98 mg/mL flavonoids in the extract was probably capable of affecting fermentation in rumen fluid, acting through bacteria selection. The dilution of propolis ethanol extract in water reduced its bacteriostatic action, given

that it lowers the content of active compounds in the diet. Propolis flavonoids, such as galangine, quercetin, pinocembrin, and kaempferol, are natural polyphenolic compounds widely spread among seed plants. Propolis also contains aromatic acids and esters, aldehydes and ketones, terpenoids and phenylpropanoids (such as caffeic and chlorogenic acids), esteroids, amino acids, polysaccharides, hydrocarbons, fatty acids, and low amounts of a number of compounds ( Bankova et al., 2000 ; Packer and Luz, 2007 ; Lustosa et al., 2008 ), which are considered as total phenols (27.65 mg/mL) in the analysis. Park et al. (1998) found that flavonoids are mostly extracted in ethanol solutions at 60 to 80% concentration, which inhibits microbial growth satisfactorily. They also report that ethanol extracts at 70 to 80% show significant antioxidant activity, similar to that observed with 100% extract in the present study , in addition to being beneficial to ruminal diet degradability and in vitro gas production. Oliveira et al. (2004) studied the effects of monensin and propolis extract on in vitro degradability of crude protein from different nitrogen sources using ruminal fluid from cattle grazing Brachiaria spp. grass. They found that both monensin and propolis extract reduced the production of ammonia from highly degradable protein sources; however, propolis was better because it reduced deamination ( Stradiotti Júnior et al., 2001 ), which can increase microbial activity and efficiency, given that rumen bacteria optimize the use of dietary nitrogen sources. This corroborates with the present study, in which in vitro degradability was higher in diets added with propolis extract . As estimated by both dual pool logistic and exponential models, extract concentration and dose also affected cumulative gas production . The negative control without propolis

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(pure ethanol) decreased gas production, likely because of its bactericidal action, which eliminated rumen fluid microorganisms. The reduction potential estimated by the dual pool logistic model was –0.32 mL of gas per milliliter of ethanol added. Similarly, the estimates provided by the exponential model indicated a negative effect of the negative control using pure ethanol, with similar reduction potential of –0.32 mL of gas per milliliter of ethanol. Alcohol acts on protein denaturation and lipid solubilization. There may be side effects on the interference of metabolism and eventual lysis of cells. Proteins can be denatured by extremes of pH and by certain miscible organic solvents such as alcohol ( Nelson and Cox, 2012 ). The result of cumulative in vitro gas production suggests that in vitro gas production increases with dose of propolis ethanol extract due to the higher dietary flavonoid and total phenol content. The maximum cumulative in vitro gas production predicted by both models using 100% ethanol extract of propolis were obtained with doses of 13.10 mL and 12.07 mL, respectively. Ítavo et al. (2011) suggested the use of brown propolis extract for 15 mL/kg DM as a substitute for sodium monensin to improve feed conversion in confined lambs. In the present study, a positive effect was obtained using 13 mL/kg DM, which reinforces the importance of in vitro analysis given that the results produced may be economically beneficial in large-scale administration. In another work, Ítavo et al (2011) concluded that different levels of green propolis extract in the diet of feedlot lambs did not influence nutrient digestibility and recommended the inclusion of 7.60 mL (2.1189 mg of dry matter and 0.1123 mg of flavonoids) of green propolis extract/day in

the diet of confined lambs to maximize efficiency,. The findings indicate that dietary propolis improves DM degradation, likely through bacterial selection by bacteriostatic action and cumulative gas production. However, the dose of extract needed to improve diet degradability is limited, as shown by the quadratic behavior of the estimates. This is probably related to the rumen environment; that is, the in vitro assay does not include factors such as passage rate and gradual extract dilution, which can impair the optimal action of propolis solutions as a diet additive because of their alcohol content. The highest gas production estimates (above 30 mL gas/100 mg fermented DM) were obtained with the diet with 100% ethanol extract of propolis. In a study on the addition of residues from alcoholic extraction of brown propolis to a ruminant diet, Heimbach et al. (2014) reported 18.18 mL in vitro gas production using a dose of 10 g/kg DM and incubation in ruminal fluid of lambs. In bovine ruminal fluid, the highest gas production they reported is 16.89 mL, obtained with diet with residue inclusion of 5 g/kg DM. The diet tested also consisted of Tifton hay combined with corn and soybean meal-based concentrate, but using a 50:50 roughage:concentrate ratio. The dose of 20 mL of 70% extract exhibited average gas production of 18.26 mL/100 mg DM, which is close to the value of 18.78 mL reported by Heimbach et al. (2014) . The difference in gas production estimates using 70 and 100% extracts and the results found by those authors are likely related to the phenol and total flavonoid content in the extracts. The propolis extraction residue tested contained 0.24 mg of total phenols and 0.35 mg of total flavonoids per gram of dry residue, whereas 100% extract exhibited 151.28 mg/mL of dry residue, 27.65 mg/mL of phenols, and 13.98 mg/mL of total

flavonoids. Given the higher phenol and flavonoid content in propolis extract compared with its residue, the higher effect of the former on ruminal fluid bacteria is expected, along with higher degradability and in vitro gas production. Thus, the diets added with 100% ethanol extract of brown propolis may lead to the greatest degradability rates and cumulative in vitro gas production. Conclusion The diets added with 100% ethanol extract of brown propolis prepared with 35 g of propolis and 65 mL of cereal alcohol promote the greatest diet degradability and cumulative in vitro gas production. Ethanol extract of brown propolis can be included as nutritional additive in ruminant diets. The maximum dose of 100% propolis extract supplementation recommended, which improves degradation and fermentation of ruminant diets, is 13 mL/kg DM. Reference - Brasil. Ministério da Saúde. Agência Nacional de Vigilância Sanitária. 2001. Legislação. Instrução Normativa n.3, de 19 de janeiro de 2001. Aprova os regulamentos técnicos de identidade e qualidade de apitoxina, cera de abelha, geléia real, pólen apícola, própolis e extrato de própolis. Brasília, DF. - Campos, F. P.; Bose, M. L. V.; Boin, C.; Lanna, D. P. D. and Morais, J. P. G. 2000. Avaliação do sistema de monitoramento computadorizado de digestão in vitro Desaparecimento da matéria seca e/ou FDN pela produção de gás. Revista Brasileira de Zootecnia 29:537-544. - Cushnie, T. P. and Lamb, A. J. 2005. Detection of galangin-induced cytoplasmic membrane damage in Staphylococcus aureus by measuring potassium loss. Journal of Ethnopharmacology 101:243-248. - Funari, C. S. and Ferro, V. O. 2006. Análise de própolis. Ciência Tecnologia

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Alimentos 26:171-178. - Ghisalberti, E. L. 1979. Propolis: a review. Bee World 60:59-84. - Goering, H. K. and Van Soest, P. J. 1970. Forage fiber analyses (apparatus, reagents, procedures, and some applications). Agriculture Handbook, 379. US Department of Agriculture, Washington, DC. - Referencia (Normas APA): Brown, T., Lemay, E., Murphy, C., Bursten, B., Woodward, P. (2014). Química, la ciencia central . (pp. 383-402, 425- 440, 513-529, 530-550). Biblioteca Virtual UNAD https://www-ebooks7-24-com.bibliotecavirtual.unad.edu.co/? il=971 Petrucci, R., Herring, F., Madura, J., Bissonnette, C. (2017). Química general principios y aplicaciones modernas . (11a. ed.). (pp. 111-137, 465-480). Biblioteca Virtual UNAD https://www-ebooks7-24- com.bibliotecavirtual.unad.edu.co/?il=5838

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