CAPE 3311 Reaction Engineering Coursework 2 Name: Sharifah Irryanti Syd Hamdan Student ID: 200802028 Date of submission : 4th December 2015 Supervisor: Dr Xiaojun Lai Question 1 To determine the holding time to produce a desired product, which is 90% R, a graph of -1/rA against CA need to be plotted. For plug flow reactor, the area under the curve represents the holding time. a) Plug flow reactor Using integration method, A = ∫_(C_A)^(C_A0)▒1/〖-r〗_A dCA = 1/k ∫_(C_A)^(C_A0)▒1/(C_A C_R ) dCA = 1/k ∫_(C_A)^(C_A0)▒1/(C_A (1-C_A)) dCA since CR =1 - CA By partial fraction, 1/(C_A (1-C_A))= A/C_A + B/〖1-C〗_A A …show more content…
So, taking CA = 2.624 mol/L as the point where the reactor change, so size ratio of first reactor, V1 and second reactor, V2 = ([( 1.6437-0.01) (2.624-0.78)])/([(0.1452-0.01) (10-2.624)]) = 3.021 Conversion rate of first reactor, CA / CA0 = (2.624/10 ) x 100% = 26.24 % Question 3 A R rR = k1CA A + A S rS = k2CA2 a) Instantaneous fractional yield of R, φ (R/A)= (moles of R formed)/(moles of A reacted) = 〖dC〗_R/(-dC_A ) = r_R/〖-r〗_A = (k_1 C_A)/(k_1 C_A+2 k_2 C_A^2 ) Instantaneous fractional yield of R, φ (R/(R+S))= r_R/(r_R+r_S )= (k_1 C_A)/(k_1 C_A+ k_2 C_A^2 ) b) Since φ (R/A)= r_R/〖-r〗_A CR max = ∫_0^(C_AO)▒〖φ 〖dC〗_A 〗 = ∫_0^(C_AO)▒〖(k_1 C_A)/(k_1 C_A+2 k_2 C_A^2 ) 〖dC〗_A 〗 = ∫_0^(C_AO)▒〖k_1/(k_1+2 k_2 C_A ) 〖dC〗_A 〗 = ∫_0^(C_AO)▒〖1/([1+(2 k_2 C_A)/k_1 ]) 〖dC〗_A 〗 CR max = k_1/〖2k〗_2 [ln〖(1+(2 k_2 C_A)/k_1 〗) ] 1¦0 = k_1/〖2k〗_2 [ln〖(1+(2 k_2)/k_1 〗) ] Let k1/k2 = K CRmax = 1- 0.18 = 0.82 mol/L CR = K/2 [ln〖(1+(2 )/K〗) ] Assume two values of K so that a graph of CR against K can be …show more content…
The second reaction, which is decomposition of Y into Z is first order reaction, n =1. X Y Z - r Y = k CY where k2 = 1.5 hr-1 Since the first reaction is of zero order, k1 = C_Y/t = (100 mol/m^3)/(0.5 hr) = 200 mol/m3hr Calculating K from k1 and k2 : K = (k_2 C_XO)/k_1 = (1.5 ( 100 ))/200 = 0.75 CYmax/ CXO = (1 - e^(-K))/K = (1 - e^(-0.75))/0.75 = 0.70351 CYmax = 0.70351 x 100 = 70.351 mol/m3 tYmax = CXO / k1 = 100/200 tYmax = 0.5 hr b) After half an hour, all X have been reacted into Y, which then dissolve into X. At t = 1 hr, only Y and Z exist. When t > C_XO/k_1 CYmax/ CXO = (1 )/K (e^(K-k_2 t-e^(-k_2 t))) = (1 )/0.75 (e^(0.75-1.5(1) )- e^(-1.5(1) )) = 0.3323 Since all X has been converted into Y and Z, so X = Y + Z CZ = [1- 0.3323] x 100 = 66.77 mol/m3 Question 5 First order A R 1. At equilibrium, K = C_R/C_A = (C_AO X_Ae)/(C_AO (1-X_Ae))=X_Ae/(1-X_Ae ) X_Ae= K (1-X_Ae) X_Ae= K – K
Question3: Experiment 3 The unknown acid sample was 1 • Monoprotic Acid Trails Initial NaOH solution (mL) final NaOH solution (mL) The volume of NaOH to titrate the acid (mL) Amount of Unknown Acid sample 1 (g) The moles of the Unknown Acid (mol) Molar mass of the Unknown Acid (g/mol) A 3.38 28.31 24.93 0.150 0.0026 57.69 B 0.18 29.32 29.14 0.175 0.0029
The reaction was repeated 3 times and average rate noted. From these rates a graph was plotted which describes the relationship of the pressure produced and number of drops added. The reaction rates were measured by Kpa/min and were written to 4 figures for precise results. Time was measured by stop watch. Table 4 shows a summary of all the groups which participated in the lab session.
What percent of oxygen is in the following compounds NO2 H2O Na2Cr2O7 A compound contains 22.1% Al, 25.4% P, and 52.4% O. What is the empirical formula of this compound? A compound contains 8.28 g C and 1.72 g H What is the empirical formula
We were able to calculate qsol, qrxn, and ΔH using: qsol= mcT qsol+qrxn=0 Hrxn=qrxnmol
To determine the rate of reaction there are many method to be used for example, measuring the mass after the product has been added and measuring the difference in mass on the duration of a digital scale. Another method, which will be used in this experiment is using a gas syringe to measure the volume of the gas which has been produced. The cylinder inside, will be pushed out to show a quantitative presentation of the volume produced by the reaction. Hypothesis
SECS 20 SECS 40 SECS 60 SECS 80 SECS 100 SECS 120 SECS TRIAL 1 0.04 0.107 0.166 0.225 0.266 0.288 0.323 TRIAL 2 0.082 1.205 0.289 0.352 0.399 0.439 0.472 TRIAL 3 0.04 0.104 0.156 0.201 0.232 0.26 0.28 pH: 5 (TRANSMITTANCE
(150.22g/mol)(3.5 x 10^-3 mol of nucleophile) = 0.525 g Actual yield = 0.441 g, Percent Yield = (0.441g/0.525g) x 100% = 84% 10. Percent recovery from recrystallization = (0.172g/0.441g) x 100% = 38% 11.
The final product weight for percent yield was only the solid E product, which missed one half of the final product produce. If both products were weight, the percent yield would have been larger that it was. Instead of 22.33%, it could have been 44.66%. To prove that both products were obtained, but only one of the two products was analyze, a TLC plate of the DCM layer, that contains both products, and of the final product, was obtain.
(0.01 moles of NaOH) x (1 mole Ca(OH)2/ 2 moles of NaOH) = 0.005 moles of Ca(OH)2 Tube 1: (0.0020 moles of CaCl2) x (1 mole Ca(OH)2/ 1 mole of CaCl2) = 0.002 moles of Ca(OH)2 (0.002 moles of Ca(OH)2) x (74.08 grams/mole) = 0.1 grams = theoretical yield Tube 2: (0.0035 moles of CaCl2) x (1 mole Ca(OH)2/ 1 mole of CaCl2) = 0.004 moles of Ca(OH)2 (0.004 moles of Ca(OH)2) x (74.08 grams/mole) = 0.3 grams= theoretical yield Tube 3 (0.0050 moles of CaCl2) x (1 mole Ca(OH)2/ 1 mole of CaCl2) = 0.005 moles of Ca(OH)2 (0.005 moles of Ca(OH)2) x (74.08 grams/mole) = 0.4 grams =theoretical yield Tube
Controlled Concentration of amylase Amount of amylase/starch Ph of the amylase/starch The concentration of the Amylase was kept at 1% at at times throughout the experiment. 5cm3 of both will be used in each reaction. pH of the Amylase/starch will be kept the same.
Predict/ roughly determine the Vmax and ½ Vmax values from the peak of the graph, where the slope of the graph levels off (the asymptotical line). Predict/ roughly determine the Km by reading off of the graph the corresponding substrate concentration on the x-axis for the ½ Vmax value. Plot a Lineweaver-Burke graph (the inverse of the velocity of the reaction vs. the inverse of the substrate concentration). Calculate accurate Vmax and Km values using the following equation for the Lineweaver-Burk
How does the amount of baking soda mixed with vinegar affect the volume of gas produced? The rate of reaction is the increase or decrease time taken at which the products are formed or concentration increase or decrease between a reaction of two or more substances. In the reaction, new bonds are formed whilst others have been broken.
℃^(-1)×6.40℃±3.1 %=1337.6 J±4.06 % ∆H=(-1337.6 J±4.06 %) /(0.025 mol ±0.16 %)= -53504 J m〖ol〗^(-1)±4.22 % ∆H=-53504 J m〖ol〗^(-1)±4.22 %÷1000=-54 kJ m〖ol〗^(-1)±4.22 % Conclusion and
The gradient gave the value of K, the rate constant for the reaction. Figure 2 shows the plotted graph Figure 2. From the
QUESTION 1 Define net price. How do you calculate the list price when the net price and trade discount rate are known? What are the steps to calculate the net price equivalent rate and then how to get the net price? What are the steps to calculate the single equivalent discount rate and then how to get the trade discount amount? Give an example of each net price equivalent rate and single equivalent discount rate.