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Thermo Answer

This document contains calculations related to thermodynamics and kinetics. It includes: 1) Calculations of temperature, pressure, volume, energy, and other properties using the gas laws and thermodynamic equations of state. 2) Derivations of heat, work, internal energy, and other thermodynamic quantities for processes like isothermal, adiabatic, isobaric, and more. 3) Applications of the ideal gas law, van der Waals equation of state, kinetic theory of gases, and other foundational relationships.
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0% found this document useful (0 votes)
51 views

Thermo Answer

This document contains calculations related to thermodynamics and kinetics. It includes: 1) Calculations of temperature, pressure, volume, energy, and other properties using the gas laws and thermodynamic equations of state. 2) Derivations of heat, work, internal energy, and other thermodynamic quantities for processes like isothermal, adiabatic, isobaric, and more. 3) Applications of the ideal gas law, van der Waals equation of state, kinetic theory of gases, and other foundational relationships.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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1.367.

Taking into account that v = (w't/c)2, we get

To— dt
yi+ (w,002 In [.`
1` ± + ) 2] = 3.5 months.
0
1.368. m/mo 1/V2 (1. --p) 70, where 13=v/c.
1.369. v (2 ri)/(1 = 0.6c, where c is the velocity
of light. The definition of density as the ratio of the rest mass of a
body to its volume is employed here.
1.370. (c — v)Ic = 1 — [1 + (m0c/p)2] -1/2 = 0.44%.
1.371. v = (chi) 1 = 1/,c
1.372. A = 0.42 m0 c2 instead of 0.14 m0c2.
1.373. v = 1/2cV 3 = 2.6.108 m/s.
1.374. For a < 1 the ratio is T/m0c2 < 4/3 0.013.
1.375. p =V T (T +2m0c2)1c = 1.09 GeV/c, where c is the velo-
city of light.
1.376. F = (I 1 ec) V T (T +2moc2), P = T I le.
1.377. p= 2nmv2/(1 — v2/c2).
1.378. v= Fct/Vmo2 c2 + F2t2, 1 =i1(moc2IF) 2 +c2t 2— M0C2/ F
1.379. F = m0c21a.
1.380. (a) In two cases: F v and F v; (b) Fl = mow V-1 —132,
mo w/(1 —p2)3/2,where 13= v/c•
1.382. 8' e 17(1 —13)/(1 +13), where f3 = V/c, V = 3/oc.
1.383. E2 — p2c2= m,;c4, where m0 is the rest mass of the par-
ticle.
1.384. (a) T = 2m0c2 (111 +7 72moc2 — 1) =777 MeV,
=---111/2/noT = 940 MeV/c; (b) V = ci/ T/(T 2m,c2) =2.12 .108 m/s.
1.385. M0-=-112mo 2m0c2)/c, V =c1/ T 1(T +2m0c2).
1.386. T' = 2T (T +2m0c2)1moc2=1.43 .103 GeV.
1.387. Ei max = ma -Fm?— (m2+ m3)2 c2. The particle mi has the
27no
highest energy when the energy of the system of the remaining
two particles m2 and m3 is the lowest, i.e. when they move as
a single whole.
oninioN2uc
'0 , Use the momentum conservation law
1.388. v/c = 1+ (nondau/c
(as in solving Problem 1.178) and the relativistic formula for
velocity transformation.
2.1. m = pV Ap/p0 =30 g, where p0 is the standard atmospher-
ic pressure.
2.2. p = 112 (piT 2ITi — Ap) = 0.10 atm.
2.3. ml/m2 = (1 — alM2)1(alMi — 1) = 0.50, where a =
mRT/pV.
Po (nil-Fr%) —1. 5 g/1
2.4. 0 RT (ml /M l -1-m2/M2)) •
2.5. (a) p = (v1 + v2 + v3) RT/V = 2.0 atm; (b) M =
v2M2 v31113)/(vi ± v2 v3) = 36.7 g/mol.
2.6. T olli 012— 1)/i (112 — 1) 0.42 kK.
In
2.7. n— In (1+ AIT/17) •
2.8. p =
2.9. t = (V/C) In 11 = 1.0 min.
2.10. AT = (mg PoAS) l/R ---- 0.9 K.
2.11. (a) Tmax = 3(PoIR)17 Pd 3a; (b) Tmax=Po/ePR.
2.12. Pmin = 2/117aTo.
2.13. dT/dh = —MgIR = —33 mK/m.
2.14. dT/dh = —Mg (n — 1)/nR.
2.15. 0.5 and 2 atm.
2.16. (a) h = RT IMg = 8.0 km; (b) h 1RTIMg = 0.08 km.
2.17. m = (1 — e -MghIRT) poSIg.
OP 00

2.18. he = .c hp dh I p dh = RTI Mg.


2.19. (a) p = Po (1 — ah.)n , h <11a; (b) p = p 01 (1 + ah)n. Here
n = MglaRT o.
2.20. p p0elt1(02r2/2RT
2.21. pid =pRTIM =80 atm; p = pRTI(M — pb) — ap2/M2=
= 80 atm.
2.22. (a) T = a (V — b) (1 + 1))/RV (QV b) = 133 K; (b)
p = RTI(V — b) — alV2 =9.9 atm.
2.23. a = V2 (T1p2 — T 2pi)I(T 2 — T1) = 185 atm•12/mo12 , b
= V — R (T 2 — T1)I(p2 — pi) = 0.042 1/mol.
2.24. x = VZ (V — b)-2/1R7T3 — 2a (V — b)2].
2.25. T > a/bR.
2.26. U = pVl•y — 1) = 10 ML
2.27. AT = 1/2/Vv2 (' — 1)/R.
2.28. T = T1T2 + P2 V2)/(PiViT2 p2V2T1); P
(PiVi P2V2)/(Vi + V2).
2.29. AU = —poVATIT 0 (7 — 1) = —0.25 kJ, Q' —AU.
2.30. Q = A?/(? — 1) = 7 J.
2.31. A = RAT = 0.60 kJ, AU = Q — RAT = 1.00 kJ,
.17 = Ql(Q — RAT) = 1.6.
2.32. Q = vRT 0 (1 — 1/n) = 2.5 kJ.
2.33. vai (v1-1)___ .33.
vl (72 —1) ± V2 (71 -1)
2.34. cy = 0.42 J/(g•K), cp = 0.65 J/(g•K).
2.35. A RT (n — 1. — ln n).
2.36. A' = PoVo In [(n + 1)2/44
2.37. y = 1 + (n — 1)1(Q1vRT, — ln n) = 1.4.
2.38. See Fig. 13 where V is an isochore, p is an isobaric line, T
is an isothermal line, and S is an adiabatic line.
2.39. (a) T = T - niv = 0.56 kK; (b) A' = RT ivy
— 1)/(y — 1) = 5.6 kJ
2.40. The work in the adiabatic process is n = (iv -
-1)/(y — 1) In n = 1.4 times greater.
2.41. T = To [(71 + 1)2/401-1)/2.
2.42. v = 112yRT1(y — 1) M = 3.3 km/s.
2.43. Q = RAT (2 — y)/(y — 1).
2.45. Cr, = R (n — 7)/(n — — 1); Cn < 0 for 1 < n < T.
2.46. C = R (n y)1 (n — 1) (y — 1) = —4.2 J/(K•mol), where
n= In 13/In a.
2.47. (a) Q = R (n — y) AT 1(n — 1) (y — 1) = 0.11 kJ; (b)
A = —RAT1(n — 1) = 0.43 kJ.

(a) (6) I
Fig. 13.

2.48. (a) AU = aV,;(112 — 1)/(y — 1); (b) A = 112aq (112— 1);


(c) C = 1/2R (y + 1)/(y — 1).
2.49. (a) C = —R/(y — 1); (b) TV(Y-1-)/2 = const; (c) A =
= 2RT0(1 — -Y)12)/(7 - 1).
2.50. (a) A = (1 — a) RAT; (b) C = R/(y — 1) + R (1 — a);
C < 0 for a > y/(y — 1).
2.51. (a) A = AU (y — 1)/a; Q = AU El (y — 1)/al; (b) C
= R1(y — 1) + R/a.
2.52. (a) C = Cv + R/aV; (b) C = Cv + R/(1 + aV).
2.53. (a) C = TR/(y — 1) + aR/P017; (b) AU = Po (V2 -
- Vi)/(y — 1); A = Po (V2 — V1) 1 a In (v 21v1); Q = w (V2
- -

— 1) + a In (V2/V1).
2.54. (a) C = Cp + RTolaV; (b) Q = aEp (V2 — V1) +
RT 0 In (V2/V1).
2.55. (a) Ve 7R = const; (b) TeR/fw = const; (c) V — aT
-21

= const.
2.56. (a) A = a In II —RT0 (1— 1)/(y —1); (b) p -VY ea (v-i)/pv,.
= const.
V2 b ( 1
2.57. A=RT In —+ —
where a and b are Van
Fi —b a V2 VI-----)

der Waals constants.


2.58. (a) AU= alV alV 2=0.11 kJ; (b) Q=RT in V2 b
- =
=3.8 kJ.
2.59. (a) T (V — b)Ricv = const;
(b) Cp —CV — I-2a (V — RTV 3 •
vaV2 (y-1)
2.60. AT= Rv, (V„-{-v,) 3.0 K.
2.61. Q = Oa (V2 — V1)1VIV2 = 0.33 kJ.
2.62. n = p/kT = 1.105 cm-3; (1) = 0.2 mm.
2.63. p = (1 mRTI MV = 1.9 atm, where M is the mass
of an N2 mole.
2.64. n = (p/kT — p/m2)/(1 — ml/m2) = 1.6.1019 cm-3, where
ml and m2are the masses of helium and nitrogen molecules.
2.65. p = 2nmv2 cost 0 = 1.0 atm, where m is the mass of a
nitrogen molecule.
2.66. i = 2/(pv2 /p — 1) = 5.
2.67. v/vn + 2)/3i; (a) 0.75; (b) 0.68.
(3N — 3) kT for volume molecules.
2.68. (8)=
(3N — 5/2) kT for linear molecules.
1/2(N-1) and 1/(2N-5/3) respectively.
2.69. (a) CV =7/2R, y = 9/7; (b) CV = (3N — 5/2) R, y
= (6N — 3)/(6N — 5); (c) Cr = 3 (N — 1) R, y =
= (N — 213)/(N — 1).
1/(3N — 2) for volume molecules,
2.70. A/Q=
1/(3N — 3/2) for linear molecules.
For monoatomic molecules A/Q = 2/5.
2.71. M = RI(cp— cv.) = 32 g/mol. i = 2/(cp/cv — 1) = 5.
2.72. (a) i = 2 (CpIR — 1) = 5; (b) i = 2 [C/R 1/(n — 1)] =
= 3, where n = 1/2 is the polytropic index.
2.73. y = (5v1 7v2)/(3v1 5v2).
2.74. Increases by Aplp = Mv2IiRT = 2.2%, where i = 5.
2.75. (a) vn=-113RTIM= 0.47 km/s, (8)= 3/2kT = 6.0-10-21 J;
(b) 3 1/2kTlapd3= 0.15 m/s.
2.76. 11= 7.6 times.
2.77. Q = 112 — 1) imRTIM = 10 kJ.
2.78. Wsq= 172kTa = 6.3 • 10 12 rad/sec.
2.79. (€),..,t = kToi2/i = 0.7.10-2° J.
2.80. Decreases 11(11-1)/1times, where i = 5.
2.81. Decreases 11(i-10-2) = 2.5 times.
2.82. C = 1/2R (i 1) = 3R.
2.83. vp , = 112p/p = 0.45 km/s, (v) = 0.51 km/s,
= 0.55 km/s.
2.84. (a) 6NIN = (8/1/n) e-161 = 1.66%;
(b) ON IN = 12 1/-3/2n e-3/28i = 1.85%.
m (Av) MV2
2.85. (a) T = —380 K; (b) T = 2k =340 K.
k -v- 2 )2
i) 3kTo •ri
2.86. (a) T — 4k ln (v2/vi ) —330 K; (b) v= V m 1-1 •
2.87. T — 2k (i AvN)m 0)2— 0.37 kK.
m
3kT 1n (m2/m1)
2.88. v = =1.61 km/s.
M2 — 1
2.89. T = 113mv21k.
2.90. dN/N = (-7 2' ) 3/2 e-mv212hT 2nvl dvl dvx.
2akT
2.91. (vx )= 0, (I vx ) =1/.2kT I nm•
2.92. (v1) = kT/m.
2.93. v =1/4r1 (v), where (v) = li8kT/am.
Co

2.94. p = 2mvx• vx dn (vx) = nkT , where dn (vx) =

(m12nkT) 1/2 n • e-m4/2hT dvx.


2.95. (1/v) =1/2mInkT = 4n (v).
2.96. dN/N= 21s (nkT)-3/2e-ena dc; ep,=1/2kT; no.
2.97. SNIN = 3 6n e-3126i= 0.9%.
CO

Q AN 231 8 e-e/kT de.


2.90 — = 1/
(nkT) 312 J
The principal contribution to the value of the integral is provided
by the smallest values of a, namely a x a o. The slowly varying factor
lii-can be taken from under the radical sign if ascribed the constant
value 1/- so. Then
AN 1 N = 2 V eolnkT e-sona
2.99. (a) vp,. = 1/3kT/m; (b) a pr =kT.
00

2.100. dv = dn (42143-t)v cos 0 = n (2kT/am)I/2sin 0 cos 0 de.


v=-0
n/2
2.101. dv = dn (d52/4n) v cos 0 = n (m/2akT)3/2 e-mv2/ 211Tv3 dv.
e=o
2.102. F = (kT I Ah) ln = 0.9.10-0 N.
2.103. NA = (6RT Ind3Apgh) ln 6.4.1023 mo1-1.
2.104. 11/10 = ec.m2-m1vninT = 1.39 .
kT In (n21%)
2.105. h —
(m2 mi) g •

2.106. Will not change.


2.107. (U) = kT. Does not depend.
2.108. w riliT I M1 N 70 g.
2RTp In 1
2.109. M —
(P— Po) (r2— r?) 0)2 •
2.110. co = V (2RT M12) ln rl = 280 rad/s.
2.111. (a) dN = no e-ar2/hT4ar2 dr; (b) kT/a; (c) dN =
= (a/akT)3/2 e-ar2/14T4TEr2 dr; (d) Will increase 13/2-fold.
2.112. (a) dN= (2nno/a3/2) e-UMT VU dU; (b) Up,=1/2kT.
2.113. In the latter case.
2.114. (a) II= 1 — ni-- ? = 0.25; (b) = 1 — ni /Y-1= 0.18.
2.115. 8 = (1 — 11)/1 = 9.
2.116. -11 = 1 — 2T3/(T1 + T2).
2.117. n = — = 60%.
2.118. 11 = 1 — n-(1-1/1)•
2.119. 71 = 1 — (n + 7)41 + yn)
2.120. In both cases 11 =1
- 1
2.121. In both cases Ti =1 n
2.122. =1 :nn •
1-"I
n 1
2.123. (a) 11=1— ‘,7 --
-

,
(b) = 1
ni — 1 y (n-1) 0-1
(n—i)
2.124. (a) 11= 1 n-1-1-(y — 1) n Inn '
n-1+(y-1)Inn
(b) it =1 y (n-1)
- (T 1) In v
2.125. —
ti In v —1)/(y —1) '
(t— 1) In n
2.126. rl =
ti In n (T-1) y/(y —1) •
2.127. 11-1 2 7+1/T
(1-1-v) (1-1-177)
2.128. The inequality .Q 1— 8Q; <0 becomes even stronger
T2
when Ti is replaced by T,,,„„ and T2 by Trnin Then Qiirmax
Q;amin< O. Hence
Qi —Q; Tnta:m—aTurin pdp
< or 1<llcarnot• (61 41
2.129. According to the Carnot theorem P
WW 1 =dTIT. Let us find the expressions
for 811 and 8Q1. For an infinitesimal Carnot
cycle (e.g. parallelogram 1234 shown in
Fig. 14)
lkfc/V
SA = dp-dV = (OpIOT)vdT • dV,
= p dV = away), + p] dV.
[( Fig. 14.
It remains to substitute the two latter expressions into the former one.
Ryln1.
2.130. (a) AS = 19 JAK • mol); (b) AS — yRy In1 n = —

= 25 J/(K • mol).
2.131. n = eAs/". = 2.0.
2.132. AS = vR ln n = 20 PK.
2.133. AS = M y-1
In n = —10 37K.
2.134. AS = In a — in 6) vR/(? — 1) = —11 J/K.
yin
2.135. 152-S1=-•vR (In a =1.0 J/K.
(n 'OR
2.136. AS =
(n-1) (v —1) In T.
2.137. AS —v(+1).R
v
71
ln a 46 J/K.
2.138. V7n Vo/a (1 +1').
2.139. T = To+ (R/a) In (V/Vo)•
2.140. AS = R In [(V2 — b)/(Vi— b)].
2.141. AS = Cv In (T2/T1) + R In [(V2— b)/(Vi — b)].
2.142. S = aT3/3.
2.143. AS = m [a In (T2/T1) + b (T 2 — T
Ti)] = 2.0 kJ/K. C>0
2.144. C = Sin; C <0 for n <0.
2.145. T = T oes-sox. See Fig. 15.
2.146. (a) C= —air; (b) Q.- a In (T1/T2);
(c) A = a In (Ti/T2) + Cv T2)• C<0
2.147. (a) = (n — 1)/2n; (b) = (n —
—1)/(n + 1).
2.148. AS = vR In n = 20 J/K. so
2.149. AU = (2Y-1— 1) RT0/(y —1), AS Fig. 15.
= R In 2.
2.150. The pressure will be higher after the fast expansion.
2.151. AS = v1R In (1 + n) + v2 R In (1 + 1/n) = 5.1 J/K.
2.152. AS = m1cl In (T/Ti) + m2c2 In (T/T 2) = 4.4 J/K, where
7' = + m2c2 T2)/(m1c1 + m2c2), c1 and c2 are the specific
heat capacities of copper and water.
+ Ts)2
2.153. AS = Cv In (T 4Ti rg >0.
2.154. (a) P .112N; (b) N — hrog(t2IT) 80, where 10-2 s is
the mean time which takes a helium atom to cover distances of
the order of the vessel's dimensions.
2.155. Op,. = Ar1/1(N/2)!P = 252. Pnia = 52p7.12N = 24.6%.
N!
2.156. Po,— • 1/32, 5/32, 10/32, 10/32, 5/32, 1/32
n! (N—n)! 2N '
respectively.
2.157. Pn=
n1ovNI where p.V /V°.
2.158. d= )376/Icn0re= 0.4 fun, where no is Loschmidt's num-
ber; (n) = 1.0 .106.
2.159. Will increase S2/00 = (1 + AT/To)iNA/2 = 101.31.10"
times.
2.160. (a) Ap = 4a/d = 13 atm; (b) Ap = 8a/d = 1.2.10-3atm.
2.161. h = 4alpgd = 21 cm.
2.162. a = 1/8pod (1. — re/n)/(112 — 1).
2.163. p = po + p gh 4a/d 2.2 atm.
2.164. h= [Po (n3— 1) + 4a (n2— 1)/d1/pg = 5 m.
2.165. Ah = 4a I cos 0 I (d2 — dOldid 2pg = 11 mm.

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