CHBE 2100 Exam 2 Fall 2019

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CHBE 2100 Exam #2, Fall 2019 page 1/1 ChBE 2100 Chemical Process Principles Fall 2019 Exam 02 There are 4 problems on this exam. There are some tables at the end of the exam that you may find useful. Please read the questions carefully. This exam is closed-book. However, you are allowed one 8.5" x 11" piece of paper with any information you want on it. These notes must be your own and may not be copied from another person. All other relevant information is provided. The use of wireless devices (e.g. cell phones, IR transmitters/receivers) is not permitted. The use of programmable calculators is only allowed if all relevant content has been erased from the calculator memory and the programmable features are not used. To receive full credit on each problem, it is advised to start with the appropriate full form of the balance equation(s) needed to solve the problem. Label all variables and equations. Include a brief word description to explain each step in your problem if appropriate. State all your assumptions clearly. Present your solution clearly. Numerical answers without units or explanations will not receive credit. Name: Section: A(9am) B(10am) C(2pm) (Please write your name on the back of the last page of the exam too) The work presented here is solely my own. | did not receive any assistance nor did | assist other students during the exam. | pledge that | have abided by the above rules and the Georgia Tech Honor Code. Signature: Problem 1 /35 Problem 2 /25 Problem 3 /15 Problem 4 125 Total /100
CHBE 2100 Exam #2, Fall 2019 page 2/10 Problem 1 (35 points) a) (2 points) The density of air increases as it flows through a tube. Under steady-state conditions, the volumetric flow rate of air at the outlet is less than / greater than / equal to the volumetric flow rate at the inlet. Explain your answer to receive credit. b) (3 points) On this phase diagram, identify which phase is present in each region. Solid: region A region B region C v 3 Liquid: region A region B region C ¢ B £ . Vapor: region A region B region C A C Temperature c) (15 points) Please answer the following questions with a brief answer of text and/or equations (i) (3 points) If a liquid is boiling, what is it vapor pressure equal to? (i) (3 points) If a single-component liquid is in equilibrium with a multicomponent vapor phase (that contains vaporized liquid), what is its vapor pressure equal to? (ii1) (3 points) A mixture of helium and benzene are in a sealed container. Initially the mixture is at its dew point. Then, the pressure is changed while the temperature is held constant. This causes the mixture to become superheated. What happened to the pressure? Why? pressure went up pressure went down pressure stayed the same Why: WP (W) 0k A-d D '8N q Y 59| T
CHBE 2100 Exam #2, Fall 2019 page 3/3 (iv) (3 points) The partition coefficient, K, of a butyl acetate/oil/water mixture is 0.28 (mass fraction of butyl acetate in oil/mass fraction of butyl acetate in water). Is butyl acetate more or less (circle one) soluble in oil than water? Explain your answer. (v) (3 points) The mole fraction of benzene is 0.2 in a two component benzene and toluene system. What is the bubble point temperature for this mixture? At this temperature, what is the vapor mole fraction of toluene? 115 110 105 Temperature (°C) 0 0.2 0.4 0.6 0.8 1.0 Mole fraction benzene P=1atm Touwoble = ___ °C Ytoluene bubble = mol toluene/mol e) (8 points) Assess the following statements by writing T (true) or F (false): - The elevation of the boiling point of a solution depends on the identity of the solute. ( - The elevation of the boiling point of a solution depends on the identity of the solvent. ( - In a solution, the higher the concentration of the solute, the higher the freezing point. ( - At higher altitudes, the boiling point of a solution is larger. ( - The vapor pressure of 1L of water at 25°C is equal to the vapor pressure of 3L of water at 25°C. ( - Water has only 1 triple point. () - If two compounds have very different vapor pressures, distillation can be used to separate them. (__) - Sea water has a lower vapor pressure than pure water. That's why sea water has a higher boiling point. () 113233142 09'0~"2t0) (N2 592 (9>
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CHBE 2100 Exam #2, Fall 2019 page 4/4 f) (7 points) During your undergraduate research work, you discovered that a newly-made solutioq was not properly labelled since it only shows the solute (glucose) and its mole fraction (Ygucose = 0.05) without naming the solvent and date of the preparation. There is another bottle containing the pure solvent, but the label is illegible. As a smart Yellow Jacket, you decide to apply your knowledge in colligative properties to identify the solvent. You measure the boiling points of the pure solvent and the glucose solution, and find that the change in boiling point of the solution is 2.61 °C. Therefore: (i) (5 points) Which of the following solvents could have been used? Justify your answer. - Acetic Acid - Water (ii) (2 points) What is the boiling point of the solution? °C R I)\e) \r\fle 1\1‘1 N
CHBE 2100 Exam #2, Fall 2019 page 5/5 Problem 2 (25 points) Contaminated soil can be remediated by injection of hot air and steam (i.e., water vapor) into the soil. To carry out this process, 30 of humid air at 100°C and 98.6 kPa with a dew point of 30°C is introduced into the contaminated soil. Once in the soil, the humid air cools to 14°C at a pressure of 109.1 kPa. Assume that all components of the soil remain in the solid state. What fraction of the water vapor originally introduced into the soil will condense after it is introduced into the soil, assuming no gas escapes from the soil. % 0 %)
CHBE 2100 Exam #2, Fall 2019 page 6/6 Problem 3 (15 points) A batch system contains 25 moles of diisopropyl ether and 75 moles of acetic acid at 1 atm and 25 °C. Upon adding water, you find that that the liquid separates into two phases: an organic phase (i.e., the phase with more diisopropyl ether) and an aqueous phase (i.e., the phase with more water). In order to dispose of this mixture, the mole fraction of diisopropy! ether should be no greater than 0.05 in the aqueous phase. Therefore, you decide to add just enough water to the mixture to achieve the target concentration in the aqueous phase. a) (5 points) Determine the mole fraction of water in the aqueous phase ___mol H,O/mol b) (6 points) Determine the number moles in the aqueous phase. ____moles ) (4 points) What is the amount (in kg) of water added? kg 100% acetic acid . e &N e s . . . R Of;\}. ‘7000 005 0.10 0.15 0.20 0.25 0.30 035 0.40 0.45 050 0.55 0.60 0.65 0.70 0.75 0.80 0.85 0.90 0.95 QQ (\9 O f\, [ @(3 'o’bo Mole frac H20 < S S\ wh'geo
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CHBE 2100 Exam #2, Fall 2019 page 7/7 Problem 4 (25 points) Toluene hydrodealkylation converts toluene (T) to benzene (B). In this process, toluene and hydrogen are converted to benzene and methane as shown in the formula below: (M (B) 1 CsHsCH3 + 1 H2 g 1 CsHs + 1 CH4 A reaction vessel for a toluene hydrodealkylation has two input streams, one containing H, gas (stream 1), and a second containing a mixture of benzene and toluene (stream 2). H, gas is flowing into the reaction vessel at a rate of 0.50 mol/min (stream 1), and a liquid mixture of benzene and toluene is flowing into the reaction vessel at 0.40 mol/min (stream 2). Inside the reaction vessel, gas (stream 3) and liquid (stream 4) phases are in equilibrium. The mole fraction of benzene in the liquid phase (stream 4)is 0.20. The system is initially at a temperature of 70°C and a pressure of 4 atm; at these conditions, the fractional conversion of toluene is negligible (i.e., there is no chemical reaction). a.) (15 points) Assume that no reaction occurs. Calculate the mole fractions of all components in the gas phase. Y3 toluene = Y3 hydrogen = y3,benzene = What are the molar flow rates of the gas and liquid streams leaving the vessel? What is the molar flow rate of toluene entering the vessel? N3 gases = mol/min Na jiquids = mol/min N2 toluene = mol/min b.) (10 points) Increasing reaction temperature typically helps reactions occur. The temperature of the reaction vessel is increased to 80°C while keeping pressure constant at 4 atm so that 50% of toluene undergoes the hydrodealkylation reaction. The flow rate and composition of streams 1 and 2 are the same as in part (a). The reaction vessel is designed such that equilibrium can be assured between exiting liquid and gas streams (after the reaction has occurred), and the molar fractions in the liquid stream are measured to be X4 penzene = 0.555, and X4 wiuene = 0.445. Determine the molar flow rate of gases leaving the reaction vessel, and give two reasons why this value is different than the value calculated in part (a). Also determine the partial pressure of CH, leaving the reactor. N3 gases = mol/min Pj3cns = atm Reason #1: Reason #2: €0t '\90 1°0"1590 ‘bhgo LOW0 ' 9tco0 (Y9800
CHBE 2100 Exam #2, Fall 2019 page 8/8 TABLE B.4 Antoine Equation Constants” B Tr+C Example: The vapor pressure of acetaldehyde at 25°C is determined as follows: 1600017 e - orvy < —_ 108, Pyi,0(25°C) = 800552 =T 591E00 2.9551 log,,p" = A p inmmHbg 7T in°C = pi,ol25°C) = 1077 = 902 mm Hg Compound Formula Range (°C) A B < Acctaldehyde C.H O 0210344 8.00552 1600017 291809 Acetic acid GHO: 298101265 7.38782 1533313 222309 Acetic acid* CH;0, 01036 718807 1416.7 225 Acctic anhydnde CyH.O5 628101394 714948 1444718 199817 Acctone 31,0 12910553 711714 1210595 229.664 Acrvlic aaid C:Hi 0, 20.0 10 70.0 5.65204 648.629 154.683 Ammonia* NH; 83 10 60 7.55466 1002711 247885 Aniline C;N 102.6 1o 185.2 7.32010 1731.515 206.049 Benzene CeHe 14.5 10 80.9 6.89272 1203531 219888 Toluene g 35301115 695805 1346773 219.693 L.1.1-Trichlorocthane CHLCl S4t016Y9 8.6434 2136.621 302.769 1.1.2-Trichlorocthane CHCl SO0t 113.7 6.95185 1314.410 209.197 Trichlorocthylene CHCl5 17.8 10 86.5 6.51827 1018.603 192.731 Vinyl acctate C:H,.O, 21.810 720 7.21010 1296.130 226.655 Water* H.0O 010 60 8.10765 1750.286 35.000 Water* H,0 60 1o 150 7.96681 1668.210 228.000 m-Xylene m-Cellyy 539.210 1400 700646 1460.183 214.827 o-Xylene o-Cilly, 63.510 1454 7.00154 1476.393 213872 p-Xylene p-Cslly 583101393 6.98320 1451.792 215111
CHBE 2100 Exam #2, Fall 2019 Table B.S Properties of Saturated Steam: Temperature Table® page 9/9 V(m’/kg) U(kJikg) H{kJ/kg) T(°C) P(bar) Water Steam Water Steam Water Evaporation Steam 0.01 0.00611 0.001000 206.2 zero 23756 +0.0 2501.6 2501.6 2 0.00705 0.001000 1799 8.4 23783 8.4 2496.8 25052 4 0.00813 0.001000 157.3 168 23811 16.8 2492.1 2508.9 6 0.00935 0.001000 137.8 252 23838 252 2487 4 25126 8 0.01072 0.001000 121.0 336 23866 336 2482.6 2516.2 10 0.01227 0.001000 106.4 420 123893 420 2477.9 2519.9 12 0.01401 0.001000 938 504 23921 504 24732 2523.6 14 0.01597 0.001001 829 588 23948 58.8 2468.5 2527.2 16 0.01817 0.001001 734 67.1 23976 67.1 2463.8 25309 18 0.02062 0.001001 65.1 75.5 24003 755 2459.0 2534.5 20 0.0234 0.001002 578 83.9 24030 839 2454.3 25382 22 0.0264 0.001002 515 922 24058 922 2449.6 2541.8 24 00298 0.001003 45.9 100.6 24085 100.6 2444.9 2545.5 25 0.0317 0.001003 434 104.8 24099 1048 24425 25473 26 0.0336 0.001003 41.0 1089 24112 1089 2440.2 2549.1 28 0.0378 0.001004 36.7 117.3 24140 1173 24354 25529 30 0.0424 0.001004 329 1257 24167 1257 2430.7 2556.4 32 00475 0.001005 29.6 1340 24194 1340 2425.9 2560.0 34 0.0532 0.001006 26.6 1424 24221 1424 24212 2563.6 36 0.0594 0.001006 240 150.7 24248 1507 2416.4 25672 38 0.0662 0.001007 21.6 159.1 24275 1591 24117 2570.8 ‘From R. W. Haywood, Thermodynamic Tables in SI (Metric) Units, Cambridge University Press, London, 1968.V = specific volume, U = specific internal energy,and # = specific enthalpy. Note: KJ/kg % 0.4303 = Buu/lb,. Table B.1 Selected Physical Property Data Compound Formula Mol. Wt. SG T (°C) BH,(T,) To(°C) AH,(T,) Tc(K) Pc(atm) ] - ) ki/mol ki/mol Ac. Acid C:H:0; 60.05 1.049 16.6 12.09 118.2 24.39 594.8 57.1 Water H;0 18.016 1.00¥ 0.00 6.0095 100.00 40.656 647.4 218.3
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CHBE 2100 Exam #2, Fall 2019 FACTORS FOR UNIT CONVERSIONS Quantity Eyuivalent Values Mass Length Volume Force Pressure 11t i 1056.68 qt 28317 em’ i ATOMIC WEIGHTS ANDNUMBERS Tkg = 1000g = 0.001 metric ton = 2.20462 b, = 35.27392 oz 1bg = 160z = 510 “ton = 453593 g = 0.453593 kg Im = 100cm = 1000 mm = 10° microns (um) = 10'” angstroms (A) 39.37in. = 32808 ft = 1.0936 yd = 0.0006214 mile 12in. = 1/3vd = 03048 m = 3048 cm tm’ = 1000L = 10°ecm® = 10° mL = 353145 ft" = 220.83 imperial gallons = 264.17 gal Lit = 1728in = 7.4805 gal = 0.028317 m’® = 28317 L IN = Tkgm's” = 107 dynes = 10° g-emis® = 0.22481 Iby Liby = 32174 Iby fUs” = 44482 N = 4.4482 % 10° dynes latm = 1.01325 % 10° N/m? (Pa) = 1.01325 % 10" dynes/cm’ 760 mm Hg at (°C (torr) = Atomic weights apply 1o naturally sccurring isotopic compositions and are based on an atomic mass of 12 Atomic Atomic Atomic Atomic Element Smbol Nambor W cight Clement Svbol Number Weight Actimum Ac 84 - Iridium Ir 7 1922 Aluminum Al 13 26915 Iron e 26 SS847 Amerikium Am s Krypton Kr 36 K380 Antimony o 1 12178 Lanthanum fa 57 13891 Argon Ar = 30948 Lawrencium Lr 103 Arsenic As 33 7406 Lead Pt 82 20719 Astatine AL 83 Lithium Li 3 £03G Barnum Ba 5n 13734 Lutctivm Lu 71 17497 Berkelium Bk 7 Magnesium Mg 12 2312 Rervibum e 4 GUI12 Manganes Mn 25 S4.9380 Hismuth %] K3 20 O Mendclevium Md 1 - Baoron n s 1081 Mercury Hg R 20059 Bromine Br 35 79.%4 Molybdenum Mo 42 9304 Cadmium «d a5 11240 Neadymium Nd o0 14424 Calcrar Ca 20 40.08 Neon Ne 10 20083 Californium [8] % - Neplunium Np a3 - Carbon 8 6 1201115 Nickel Ni P2 871 Cerum Ce Rt ] 140012 Niobium Nh 41 92906 Cosium s 55 132U Nitrogen N 7 140067 Chlonng 1 17 35353 Nobzlium No 102 Chromium Cr p2 | $1.%96 Osmium n 75 1902 obait (o pa) SN 0332 Uxypen (8] 1 189993 Copper Cu bl 63540 Palladium ra 46 106.4 Curium Cm 9% Phosphorus 4 1s U573 Dysprosium Dy 0 162.50 Platinum [ 195.00 Einsteinium Es (2] - Plutomium Py 94 - Erbium Fr (2] 16726 Polonium o 54 Furopium Fu [l 151 9% Potassium K 19 VR (1] Formuum Fm 1w ~ Prascodymium Pr 4 JEAT i Flucring I 9 IR9RE Promethium Pm 6l Francium Ir 87 Protsctinium " 9l Gadodinium G (2] 15728 Radium Ra XK Coathum o i w7 Radon Rn L - Guormanium Ge 32 728 Rhenium Re Al 1862 Crald Au 9 196,967 Rhodium Rh 44 1. Hatnwm H n 178 40 Rubidium Rb 37 BLS7 Helwm He 1002 Rathcnmum Ru 14 107 Holmwen Ho 67 1624.9% Samarium Sm a2 15035 Hydrogen H i LOO797 Scambium S 2 4495 = 101.325 kPa = 1.01325 bar 10.333 m H2O at 4°C THE GAS CONSTANT 8314 m*-Pa’(mol-K) 0.08314 L-bar/(mol-K) 0.08206 L-atm/(mol-K) 62.36 L-mm He/(mol-K} 0.7302 ' -atm/{Ib-mole -°R) 10.73 ft*- psia/(1b-mole “R ) 8.314 Jimol-K) LOX7 cal/{mol-K} L987 Bu/(Ib-mole-*R) page 10/10