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ch03 PDF
ch03 PDF
16 × 6 × 2 m3 1000 kg
3.1 (a) m =
m 3 b
≈ 2 × 10 5 2 103 ≈ 2 × 105 kg gb gb gd i
8 oz 1 qt 106 cm3 1g 4 × 106
(b) m = ≈ ≈ 1 × 102 g / s
2s 32 oz 1056.68 qt cm 3
b3 × 10gd10 i
3
(d) dictionary
πD 2 L 314
. 4.5 ft 2 2
800 miles 5880 ft 7.4805 gal 1 barrel
V= =
4 4 1 mile 1 ft 3 42 gal
≈
d i d
3 × 4 × 5 × 8 × 10 2 × 5 × 10 3 × 7 i ≈ 1 × 10 7 barrels
4 × 4 × 10
995 kg 1 lb m 0.028317 m3
3.2 (a) (i) 3 3
= 62.12 lb m / ft 3
m 0.45359 kg 1 ft
995 kg / m3 62.43 lb m / ft 3
(ii) = 62.12 lb m / ft 3
1000 kg / m3
50 L 0.70 × 103 kg 1 m3
3.3 (a) = 35 kg
m3 103 L
3-1
3.3 (cont’d)
(d) Assuming that 1 cm3 kerosene was mixed with Vg (cm3 ) gasoline
d i d
Vg cm3gasoline ⇒ 0.70Vg g gasoline i
1dcm kerosenei ⇒ 0.82dg kerosenei
3
SG =
d0.70V + 0.82idg blendi = 0.78 ⇒ V
g
=
0.82 − 0.78
= 0.5 0 cm
3
50.0 kg L 5 Fr $1
3.4 In France: = $68.42
0.7 × 10
. kg 1L 5.22 Fr
50.0 kg L 1 gal $1.20
In U.S.: = $22.64
0.70 × 10
. kg 3.7854 L 1 gal
3.5
VB ( ft 3 / h ), m B ( lb m / h )
V ( ft 3 / h), SG = 0.850
VH ( ft 3 / h ), m H ( lb m / h ) 700 lb m / h
700 lb m ft 3
(a) V = = 1319
. ft 3 / h
h 0.850 × 62.43 lb m
V ft
m B = B
3
d i
0.879 × 62.43 lb m kg / h
= 54.88V b g
h bg ft 3
B
d hb
m = V 0.659 × 62.43 = 4114
H H . V kg / hg H b g
VB + VH = 1319
. ft 3 / h
m B + m H = 54.88VB + 4114
. VH = 700 lb m
⇒ V = 114 B . ft 3 / h ⇒ m = 628 lb / h benzene
B m
3-2
195.5 kg H 2SO 4 1 kg solution L
3.6 (a) V = = 445 L
0.35kg H 2SO 4 12563
. × 1000
. kg
(b)
195.5 kg H 2 SO 4 L
Videal =
18255
. × 1.00 kg
195.5 kg H 2 SO 4 0.65 kg H 2 O L
+ = 470 L
0.35 kg H 2 SO 4 1.000 kg
470 − 445
% error = × 100% = 5.6%
445
3.7 b gE
Buoyant force up = Weight of block down b g
Mass of oil displaced + Mass of water displaced = Mass of block
b g b
ρ oil 0.542 V + ρ H O 1 − 0.542 V = ρ c V
2
g
From Table B.1: ρ c = 2.26 g / cm3 , ρ w = 100
. g / cm3 ⇒ ρ oil = 3.325 g / cm3
moil = ρ oil × V = 3.325 g / cm3 × 35.3 cm3 = 117.4 g
moil + flask = 117.4 g + 124.8 g = 242 g
3.8 b g
Buoyant force up = Weight of block down b g
⇒ Wdisplaced liquid = Wblock ⇒ ( ρVg ) disp. Liq = ( ρVg ) block
Expt. 1: ρ w 15 b g
. A g = ρB 2A g ⇒ ρB = ρw × b g 15
2
.
ρ w =1.00 g/cm3
ρ B = 0.75 g / cm3 ⇒ SG b g B
= 0.75
bg b g
Expt. 2: ρ soln A g = ρ B 2 A g ⇒ ρ soln = 2 ρ B = 15
. g / cm3 ⇒ SG b g soln
= 15
.
3.9
Let ρ w = density of water. Note: ρ A > ρ w (object sinks)
2.05 kg 50 L 9.807 m / s2 1N
(b) Wbag = ρ bulkVg = = 100
. × 103 N
L 1 kg ⋅ m / s 2
Neglected the weight of the bag itself and of the air in the filled bag.
(c) The limestone would fall short of filling three bags, because
– the powder would pack tighter than the original particles.
– you could never recover 100% of what you fed to the mill.
3-4
122.5 kg 9.807 m / s2 1N
3.11 (a) Wb = mb g = = 1202 N
1 kg ⋅ m / s2
Wb − WI (1202 N - 44.0 N) 1 kg ⋅ m / s2
Vb = = = 119 L
ρwg 0.996 kg / L × 9.807 m / s2 1N
m 122.5 kg
ρb = b = = 103
. kg / L
Vb 119 L
f
+
ρ nf JK ρ b
b
⇒ xf GH ρ f
−
1
ρ nf JK ρ ρ
b nf
⇒ xf =
1 / ρ f − 1 / ρ nf
1 / ρ b − 1 / ρ nf . − 1 / 1.1
1 / 103
(c) x f = = = 0.31
1 / ρ f − 1 / ρ nf 1 / 0.9 − 1 / 1.1
f
−
ρ nf JK lungs + Vother ) = mb GH ρ ρ JK
b nf
F 1 − 1 I = 1 − 1 − V +V
GH ρ ρ JK ρ ρ
⇒ xf
f m nf b nf
lungs
b
other
F 1 − 1 I − F V + V I F 1 1 I F 12. + 01. I
GH ρ ρ JK GH m JK GH 1.03 − 11. JK − GH 122.5 JK
b nf
lungs
b
other
⇒x = = = 0.25
f
F1− 1I FG 1 − 1 IJ
GH ρ ρ JK H 0.9 11. K f nf
3-5
3.12 (a)
4.5
. ρ − 539.03
From the plot above, r = 5455
(c) The measured solution density is 0.9940 g ILE/cm3 solution at 50oC. For the calculation
of Part (b) to be correct, the density would have to be changed to its equivalent at 47oC.
Presuming that the dependence of solution density on T is the same as that of pure water,
the solution density at 47oC would be higher than 0.9940 g ILE/cm3. The ILE mass flow
rate calculated in Part (b) is therefore too low.
3.13 (a)
1.20
1.00
Mass Flow Rate (kg/min)
y = 0.0743x + 0.1523
R 2 = 0.9989
0.80
0.60
0.40
0.20
0.00
0.0 2.0 4.0 6.0 8.0 10.0 12.0
Rotameter Reading
3-6
3.13 (cont’d)
b g
From the plot, R = 5.3 ⇒ m = 0.0743 5.3 + 01523
. = 0.55 kg / min
(b)
Rotameter Collection Collected Mass Flow Difference Mean Di
Reading Time Volume Rate Duplicate
(min) (cm3) (kg/min) (Di)
2 1 297 0.297
2 1 301 0.301 0.004
4 1 454 0.454
4 1 448 0.448 0.006
6 0.5 300 0.600
6 0.5 298 0.596 0.004 0.0104
8 0.5 371 0.742
8 0.5 377 0.754 0.012
10 0.5 440 0.880
10 0.5 453 0.906 0.026
1
Di =
5
b g
0.004 + 0.006 + 0.004 + 0.012 + 0.026 = 0.0104 kg / min
3-7
175 m3 1000 L 0.866 kg 1h
3.15 (a) m = 3
= 2526 kg / min
h m L 60 min
3-8
3.20 (a)
Unit Function
Crystallizer Form solid gypsum particles from a solution
Filter Separate particles from solution
Dryer Remove water from filter cake
0.35 kg C aSO 4 ⋅ 2 H 2 O
(b) m gypsum = 1 L slurry = 0 .35 kg C aSO 4 ⋅ 2 H 2 O
L slurry
0.35 kg CaSO4 ⋅ 2H2OL CaSO4 ⋅ 2H2O
Vgypsum = = 0151
. L CaSO4 ⋅ 2H2O
2.32 kg CaSO4 ⋅ 2H2O
0.35 kg gypsum 136.15 kg CaSO 4
CaSO 4 in gypsum: m = = 0.277 kg CaSO 4
172.18 kg gypsum
CaSO 4 in soln.: m =
b1− 0151
. g L sol 1.05 kg 0.209 kg CaSO 4
= 0.00186 kg CaSO 4
L 100.209 kg sol
3.21
45.8 L 0.90 kg kmol
= 0.5496
kmol U|
CSA:
min L 75 kg min
⇒
|V
0.5496
= 1.2
mol CSA
FB:
55.2 L 0.75 kg kmol
= 0.4600
kmol ||
0.4600 mol FB
min L 90 kg min W
She was wrong.
The mixer would come to a grinding halt and the motor would overheat.
3-9
0.09 mol CH 4
16.04 g 0.91 mol Air 29.0 g Air
3.23 M = + = 27.83 g mol
mol mol
700 kg kmol 0.090 kmol CH 4
= 2.264 kmol CH 4 h
h 27.83 kg 1.00 kmol mix
2.264 kmol CH 4 0.91 kmol air
= 22.89 kmol air h
h 0.09 kmol CH 4
2.264 kmol CH 4 0.95 kmol air
5% CH 4 ⇒ = 43.01 kmol air h
h 0.05 kmol CH 4
mi m M
3.24 xi = , ρi = i , ρ =
M Vi V
mi mi 1 mi2
A: ∑ xi ρi = ∑ M Vi
=
M
∑V ≠ρ Not helpful.
i
xi mi Vi 1 V 1
B: ∑ρ = ∑M m
=
M
∑ Vi = M = ρ Correct.
i i
1 xi 0.60 0.25 0.15
ρ
= ∑ = + +
ρ i 0.791 1.049 1.595
= 1.091 ⇒ ρ = 0.917 g / cm 3
R|20 × 80 = 64 mol CO
⇒S
2
3.25 (a) Basis: 100 mol N 2 ⇒ 20 mol CH 4 25
|T 20 × 40
25
= 32 mol CO
32 64
xCO = = 0.15 m ol C O / m ol , x C O 2 = = 0.30 m ol C O 2 / m ol
216 216
20 100
x CH 4 = = 0.09 mol CH 4 / mol , x N 2 = = 0.46 mol N 2 / mol
216 216
(b) M = ∑ yi M i = 015
. × 28 + 0.30 × 44 + 0.09 × 16 + 0.46 × 28 = 32 g / mol
3-10
3.26 (a)
Samples Species MW k Peak Mole Mass moles mass
Area Fraction Fraction
1 CH4 16.04 0.150 3.6 0.156 0.062 0.540 8.662
C2H6 30.07 0.287 2.8 0.233 0.173 0.804 24.164
C3H8 44.09 0.467 2.4 0.324 0.353 1.121 49.416
C4H10 58.12 0.583 1.7 0.287 0.412 0.991 57.603
3-11
3.26 (cont’d)
(8.7 × 10 6 × 0.40) kg C 44 kg CO 2
3.27 (a) = 1.28 × 10 7 kg CO 2 ⇒ 2.9 × 105 kmol CO 2
12 kg C
. × 10 6 × 0.26) kg C 28 kg CO
(11
= 6.67 × 10 5 kg CO ⇒ 2.38 × 10 4 kmol CO
12 kg C
( 3.8 × 10 5 × 0.10) kg C 16 kg CH 4
= 5.07 × 10 4 kg CH 4 ⇒ 3.17 × 10 3 kmol CH 4
12 kg C
(1.28 × 10 7 + 6.67 × 10 5 + 5.07 × 10 4 ) kg 1 metric ton metric tons
m= = 13,500
1000 kg yr
M = ∑y i M i = 0.915 × 44 + 0.075 × 28 + 0.01 × 16 = 42.5 g / mol
3-12
3.28 (cont’d)
55 gal 3.7854 L min 60 s
(b) t = V = = 144 s
V gal 87 L min
55 gal 3.7854 L 10 3 mL 1.03 g 0.0500 g H 2 SO 4 1 lbm
= 23.6 lb m H 2 SO 4
gal 1L mL g 453.59 g
V 87 L m 3 1 min
(c) u = = = 0.513 m / s
A min 1000 L 60 s (π × 0.06 2 / 4 ) m 2
L 45 m
t= = = 88 s
u 0.513 m / s
3.29 (a)
1.50 L C6H14(l)/min
n 3 (mol C6H14(l)/min)
n3 1147
.
(b) Hexane recovery = × 100% = × 100% = 76%
n1 0180
. 838 . b g
30 mL 1L 0.030 mol 172 g
3.30 = 0155
. g Nauseum
103 mL lL 1 mol
3-13
3.31 (a) kt is dimensionless ⇒ k (min -1 )
(b) A semilog plot of CA vs. t is a straight line ⇒ ln CA = ln CAO − kt
1 y = -0.4137x + 0.2512
0
-1 R2 = 0.9996
ln(CA) -2
-3
-4
-5
0.0 5.0 10.0
t (m in)
k = 0.414 min −1
ln CAO = 02512
. ⇒ CAO = 1286
. lb - moles ft 3
t ′bsg 1 min
t bming = = t ′ 60
60 s
C A = C A 0 exp(− kt )
b g b g b g
drop primes
0.06243C A′ = 1334
. exp −0.419t ′ 60 ⇒ C A mol / L = 214
. exp −0.00693t
t = 200 s ⇒ C A = 5.30 mol / L
280 cm Hg 10 mm 101325
. × 106 dynes cm2 1002 cm2 dynes
(d) = 3.733 × 1010
1 cm 760 mm Hg 2
1 m 2
m2
20 cm Hg 10 mm 1 atm
(e) 1 atm − = 0.737 atm
1 cm 760 mm Hg
3-14
3.32 (cont’d)
(f)
25.0 psig 760 mm Hg gauge b g = 1293 mm Hg bgaugeg
14.696 psig
(g)
b25.0 + 14.696gpsi 760 mm Hg
= 2053 mm Hg abs b g
14.696 psi
⇒ h (m) = 0111
. Pg (kPa)
Pg
Pg = 68 kPa ⇒ h = 0111
. × 68 = 7.55 m
FG
moil = ρV = 0.92 × 1000
kg IJ FG
π
16 2 3 IJ
H m3
× 7.55
K H
× ×
4
m = 14
. × 10 6 kg
K
(b) Pg + Patm = Ptop + ρgh
b g b g
68 + 101 = 115 + 0.92 × 1000 × 9.81 / 103 h ⇒ h = 5.98 m
3-15
3.35 b g
Δ P = Patm + ρgh − Pinside
= 1 atm − 1 atm +
b105
. g1000 kg 9.8066 m 150 m 12 m2 1N
m3 s2 1002 cm2 1 kg ⋅ m / s2
F=
154 N 65 cm2
= × ×
022481
. FG
lb f
= 2250 lb f
IJ
H K
4
100
. 10 N
cm2 1N
. × 62.43 lb m
14 1 ft 3 2.3 × 106 gal
3.36 m = ρV = 3
= 2.69 × 107 lb m
ft 7.481 gal
P = P0 + ρgh
. × 62.43 lb m 32.174 ft 30 ft
lb f 14 1 lb f 12 ft 2
= 14.7 2 +
in ft 3 s2 32.174 lb m ⋅ ft / s2 12 2 in 2
= 32.9 psi
π × 24 2 × 3 in 3 1 ft 3 8.0 × 62.43 lb m
3.37 (a) mhead = 3 3
= 392 lb m
4 12 in ft 3
392 lb m 32.174 ft / s 2 1 lb f
W = mhead g = = 392 lb f
32.174 lb m ⋅ ft / s 2
⎡⎣( 30 + 14.7 ) ⎤⎦ lb f π × 202 in 2
Fnet = Fgas − Fatm − W =
in 2 4
14.7 lbf π × 242 in 2
− 2 − 392 lb f = 7.00 × 103 lbf
in 4
F 7.000 × 10 lbf 3
32.174 lb m ⋅ ft/s 2
Initial acceleration: a = net = = 576 ft/s 2
mhead 392 lb m 1 lb f
(b) Vent the reactor through a valve to the outside or a hood before removing the head.
3-16
3.38 (a)
Pa = ρgh + Patm , Pb = Patm
If the inside pressure on the door equaled Pa , the force on
the door would be F = Adoor ( Pa − Pb ) = ρghAdoor
a Since the pressure at every point on the door is greater than
2m b
Pa , Since the pressure at every point on the door is greater
1m
than Pa , F >ρghAdoor
(b) Assume an average bathtub 5 ft long, 2.5 ft wide, and 2 ft high takes about 10 min to
fill.
V 5 × 25
. × 2 ft 3
Vtub = ≈ . ft 3 / min ⇒ V = 5 × 25
= 25 . = 125
. ft 3 / min
t 10 min
dP i g =
b g
25 + 5 m H 2 O 101.3 kPa
= 294 kPa
junction 10.33 m H 2 O
(c) The line could be clogged, or there could be a leak between the junction and the tap.
3-17
b g
3.41 (a) P1 + ρ A g h1 + h2 = P2 + ρ B gh1 + ρ C gh2
b g
⇒ P1 − P2 = ρ B − ρ A gh1 + ρ C − ρ A gh2b g
(b) P1 = 121 kPa +
LMb10. − 0.792g g 981 cm 30.0 cm + b137 . − 0.792g g 981 cm 24.0 cmOP
N cm s 3 2
cm 3
s2 Q
F 1 dyne I F
×G
I = 123.0 kPa
H 1 g ⋅ cm / s K H 1.01325 × 10 dynes / cm JK
J G 101325
. kPa
2 6 2
3.42 (a) Say ρt (g/cm3) = density of toluene, ρm (g/cm3) = density of manometer fluid
500 − h
ρ t g (500 − h + R ) = ρ m gR ⇒ R =
ρm
−1
ρt
(i) Hg: ρ t = 0.866, ρ m = 13.6, h = 150 cm ⇒ R = 238
. cm
(ii) H 2 O: ρ t = 0.866, ρ m = 100
. , h = 150 cm ⇒ R = 2260 cm
Use mercury, because the water manometer would have to be too tall.
(b) If the manometer were simply filled with toluene, the level in the glass tube would be at
the level in the tank.
Advantages of using mercury: smaller manometer; less evaporation.
(c) The nitrogen blanket is used to avoid contact between toluene and atmospheric oxygen,
minimizing the risk of combustion.
3.43 gb
Patm = ρ f g 7.23 m ⇒ ρ f =
P
7.23 g
atm
⇒ Pa − Pb = 81
. mm Hg
. psi 760 mm Hg
75
3.44 (a) Δh = 900 − hl = = 388 mm Hg ⇒ hl = 900 − 388=512 mm
14.696 psi
3-18
3.45 (a) h = L sin θ
b g b g
(b) h = 8.7 cm sin 15° = 2.3 cm H 2 O = 23 mm H 2 O
= 393 mm Hg
b g
(b) lnV = n ln ΔP + ln K
4.5
4
-2.5 -2 -1.5 -1 -0.5 0
ln( P)
3-19
3.47 (cont’d)
b gb g
(c) h = 23 ⇒ ΔP = 0.02274 23 = 0.523 mm Hg ⇒ V = 183 0.523 b g 0.5
= 132 mL s
132 mL 0.791 g 104 g 1 mol
= 104 g s = 180
. mol s
s mL s 58.08 g
85° C 10
. °K 85° C 18
. °F 85° C 1.8° R
(c) ΔT = = 85° K; = 153° F; = 153° R
. °C
10 1° C . °C
10
D D
(c) T1 = 15D C ⇒ 100D L ; T2 = 43 C ⇒1000 L
T (D C) = aT (D L) + b
a=
b43 − 15gD C = 0.0311FG D C IJ ; . DC
b = 15 − 0.0311 × 100 = 119
b1000 - 100gD L H D LK
T (D C) = 0.0311T (D L) + 11.9 and
⇒
T (D L) =
1
⎡0.0940T (o FB)+4.00-11.9 ⎤⎦ = 3.023T (o FB)-254
0.0311 ⎣
3-20
3.50 bT g = 100° C bT g
b H 2O m AgCl = 455° C
(a) V b mVg = aT b° Cg + b
5.27 = 100a + b a = 0.05524 mV ° C
⇒
24.88 = 455a + b b = −0.2539 mV
b g
V mV = 0.05524T ° C − 0.2539 b g
⇓
b g
T ° C = 1810
. V mV + 4.596 b g
. mV→136
(b) 100 . mV ⇒1856
. °C →2508
. °C ⇒ =
b . − 1856
dT 2508 g
. °C
= 326
. °C / s
dt 20 s
3.51 (a) ln T = ln K + n ln R T = KR n
n=
b
ln 250.0 110.0 g = 1184
b
ln 40.0 20.0 g .
ln K = ln 1100
. − 1184 . ) = 1154
. (ln200 . ⇒ K = 3169
. ⇒T = 3169
. R1184
.
F 320 IJ
(b) R = G
1/1.184
H 3169
. K
= 49.3
Pbatmg =
b g P′ psig + 14696
.
bg d i
, V L = V ′ ft ×
. ft 3
28317
3
.
14696 L
T ′(D F) − 32
b g b
n mol = n ′ lb - moles × g 453.59 mol
lb − moles
, T(D K) =
1.8
+ 27315
.
⇒
b P′ + 14.696g × V ′ × 28317 = 0.08206 × n ′ ×
453.59 L (T ′ − 32)
×M
O
. P
+ 27315
14.696
.
1 N 1.8 Q
0.08206 × 14.696 × 453.59
b
⇒ P ′ + 14.696 × V ′ = g 28.317 × 18.
b
× n ′ × T ′ + 459.7 g
b g
⇒ P′ + 14.696 V ′ = 1073
. n′ T ′ + 459.7 b g
3-21
3.52 (cont’d)
′ =
b500 + 14.696g × 35. = 0.308 lb - mole
10.73 × b85 + 459.7g
(b) ntot
(c) T ′ =
b3000 + 14.696g × 35. − 459.7 = 2733D F
10.73 × 0.308
b g b
3.53 (a) T ° C = a × r ohms + b g
0 = 23624
. a +b UV ⇒ a = 10634
.
b g
⇒ T ° C = 10634 b g
. r ohms − 25122
.
. a + bW
100 = 33028 b = −25122
.
n ′ 12186
=
. P′ V ′
⇒ n ′ =
.
0016034 b g d
P′ mm Hg V ′ m3 min i
60 760 T ′ + 27316
. 60 b g
T ′ ° C + 27316
.
r1 = 26159
. ⇒ T1 = 26.95° C
⇒ r2 = 26157
. ⇒ T2 = 26.93° C
r3 = 44.789 ⇒ T3 = 2251
. °C
⇒ h2 = 156 mm ⇒ P2 = 9119
. mm Hg
h3 = 74 mm ⇒ P3 = 829.9 mm Hg
3-22
3.53 (cont’d)
(d) n1 =
b0.016034gb987.9gb947 60g = 0.8331 kmol CH min
26.95 + 27316
4
.
n2 =
b0.016034gb9119. gb195g = 9.501 kmol air min
26.93 + 27316
.
n3 = n1 + n2 = 10.33 kmol min
(e) V3 =
b
n3 T2 + 27316
. g b
=
gb. + 27316
10.33 2251 . g
= 387 m3 min
0.016034 P3 b gb
0.016034 829.9 g
0.8331 kmol CH 4 16.04 kg CH 4 kg CH 4
(f) = 13.36
min kmol min
0.21× 9.501 kmol O2 32.0 kg O2 0.79 × 9.501 kmol N2 28.0 kg N2 kg air
+ = 274
min kmol O2 min kmol N2 min
13.36 kg CH 4 min
xCH4 = = 0.0465 kg CH 4 kg
(13.36 + 274) kg / min
3-23
3.54 (cont’d)
4 CONTINUE
CALL LS (X, Y, NT, SLOPE, INTCPT)
b
KO = EXP INTCPT g
E = −8.314 = SLOPE
WRITE (6, 5) KO, E
2 FORMAT (' TEMPERATURE (K): ', F6.2, /
* ' TIME CA', /,
* ' (MIN) (MOLES)', /
* 100 (IX, F5.2, 3X, F7.4, /))
3 FORMAT (' K (L/MOL – MIN): ', F5.3, //)
5 FORMAT (/, ' KO (L/MOL – MIN) : ', E 12.4, /, ' E (J/MOL): ', E 12.4)
END
SUBROUTINE LS (X, Y, N, SLOPE, INTCPT)
REAL X(100), Y(100), SLOPE, INTCPT, SX, SY, SXX, SXY, AN
INTEGER N, J
SX=0
SY=0
SXX=0
SXY=0
DO 10 J=1,N
SX = SX + X(J)
SY = SY + Y(J)
SXX = SXX + X(J)**2
SXY = SXY + X(J)*Y(J)
10 CONTINUE
AN = N
SX = SX/AN
SY = SY/AN
SXX = SXX/AN
SXY = SXY/AN
SLOPE = (SXY – SX*SY)/(SXX – SX**2)
INTCPT = SY – SLOPE*SX
RETURN
END
$ DATA [OUTPUT]
65.0 4 TEMPERATURE (K): 367.15
94.0 6 TIME CA
10.0 8.1 (MIN) (MOLS/L)
20.0 4.3 10.00 0.1246
30.0 3.0 20.00 0.0662
40.0 2.2 30.00 0.0462
50.0 1.8 40.00 0.0338
3-24
3.54 (cont’d)
b g
K L / MOL ⋅ MIN : 0.707 bat 94°Cg
110. 6
10.0 3.5
20.0 1.8 TEMPERATURE (K): 383.15
30.0 1.2 #
40.0 0.92 b g
K L / MOL ⋅ MIN : 1.758
50.0 0.73
60.0 0.61 #
127. 6
# b g
K0 L / MOL − MIN : 0.2329E + 10
# ETC E bJ / MOLg: 0.6690E + 05
3-25