2-200

TABLE 2-179 Enthalpies and Gibbs Energies of Formation, Entropies, and Net Enthalpies of Combustion of Inorganic and Organic Compounds at 298.15 K (Concluded)
Ideal gas enthalpy Ideal gas Gibbs energy Ideal gas Standard net enthalpy
Cmpd. of formation, of formation, entropy, of combustion,
no. Name Formula CAS no. Mol. wt. J/kmol × 1E-07 J/kmol × 1E-07 J/(kmolK) × 1E-05 J/kmol × 1E-09
301 Propionitrile C3H5N 107-12-0 55.079 5.18 9.74949 2.8614 −1.8007
302 Propyl acetate C5H10O2 109-60-4 102.132 −46.48 −32.04 4.023 −2.672
303 Propyl amine C3H9N 107-10-8 59.110 −7.05 4.17 3.242 −2.165
304 Propylbenzene C9H12 103-65-1 120.192 0.79 13.76 4.0014 −4.95415
305 Propylene C3H6 115-07-1 42.080 2.023 6.264 2.67 −1.9262
306 Propyl formate C4H8O2 110-74-7 88.105 −40.76 −29.36 3.678 −2.041
307 2-Propyl mercaptan C3H8S 75-33-2 76.161 −7.59 −0.218 3.243 −2.3398
308 Propyl mercaptan C3H8S 107-03-9 76.161 −6.75 0.2583 3.365 −2.3458
309 1,2-Propylene glycol C3H8O2 57-55-6 76.094 −42.15 −30.4 3.52 −1.6476
310 Quinone C6H4O2 106-51-4 108.095 −12.29 −6.92 3.205 −2.658
311 Silicon tetrafluoride F4Si 7783-61-1 104.079 −161.494 −157.27 2.82651 0.7055
312 Styrene C8H8 100-42-5 104.149 14.74 21.39 3.451 −4.219
313 Succinic acid C4H6O4 110-15-6 118.088 −82.29 −69.73 4.034 −1.3591
314 Sulfur dioxide O2S 7446-09-5 64.064 −29.684 −30.012 2.481
315 Sulfur hexafluoride F6S 2551-62-4 146.055 −122.047 −111.653 2.91625 0.924
316 Sulfur trioxide O3S 7446-11-9 80.063 −39.572 −37.095 2.5651 0.1422
317 Terephthalic acid C8H6O4 100-21-0 166.131 −71.79 −59.9 4.48 −3.0576
318 o-Terphenyl C18H14 84-15-1 230.304 27.66 42.3 5.263 −9.053
319 Tetradecane C14H30 629-59-4 198.388 −33.244 6.599 7.0259 −8.73282
320 Tetrahydrofuran C4H8O 109-99-9 72.106 −18.418 −7.969 2.9729 −2.325
321 1,2,3,4-Tetrahydronaphthalene C10H12 119-64-2 132.202 2.661 16.71 3.6964 −5.3575
322 Tetrahydrothiophene C4H8S 110-01-0 88.171 −3.376 4.59 3.1 −2.76549
323 2,2,3,3-Tetramethylbutane C8H18 594-82-1 114.229 −22.56 2.239 3.893 −5.0639
324 Thiophene C4H4S 110-02-1 84.140 11.544 12.67 2.784 −2.4352
325 Toluene C7H8 108-88-3 92.138 5.017 12.22 3.2099 −3.734
326 1,1,2-Trichloroethane C2H3Cl3 79-00-5 133.404 −14.2 −8.097 3.371 −0.9685
327 Tridecane C13H28 629-50-5 184.361 −31.177 5.771 6.6337 −8.1229
328 Triethyl amine C6H15N 121-44-8 101.190 −9.58 11.41 4.054 −4.0405
329 Trimethyl amine C3H9N 75-50-3 59.110 −2.431 9.899 2.87 −2.2449
330 1,2,3-Trimethylbenzene C9H12 526-73-8 120.192 −0.95 12.61 3.805 −4.934
331 1,2,4-Trimethylbenzene C9H12 95-63-6 120.192 −1.38 11.71 3.961 −4.9307
332 2,2,4-Trimethylpentane C8H18 540-84-1 114.229 −22.401 1.394 4.2296 −5.06528
333 2,3,3-Trimethylpentane C8H18 560-21-4 114.229 −21.845 1.828 4.2702 −5.06876
334 1,3,5-Trinitrobenzene C6H3N3O6 99-35-4 213.105 6.24 26.79 4.435 −2.6867
335 2,4,6-Trinitrotoluene C7H5N3O6 118-96-7 227.131 4.34 28.44 4.607 −3.2959
336 Undecane C11H24 1120-21-4 156.308 −27.043 4.116 5.8493 −6.9036
337 1-Undecanol C11H24O 112-42-5 172.308 −41.9 −9.177 6.363 −6.726
338 Vinyl acetate C4H6O2 108-05-4 86.089 −31.49 −22.79 3.28 −1.95
339 Vinyl acetylene C4H4 689-97-4 52.075 30.46 30.6 2.794 −2.362
340 Vinyl chloride C2H3Cl 75-01-4 62.498 2.845 4.195 2.7354 −1.178
341 Vinyl trichlorosilane C2H3Cl3Si 75-94-5 161.490 −48.116 −42.5514 3.73966 −1.544
342 Water H2O 7732-18-5 18.015 −24.1814 −22.859 1.88724
343 m-Xylene C8H10 108-38-3 106.165 1.732 11.876 3.5854 −4.3318
344 o-Xylene C8H10 95-47-6 106.165 1.908 12.2 3.5383 −4.333
345 p-Xylene C8H10 106-42-3 106.165 1.803 12.14 3.52165 −4.333
The compounds are considered to be formed from the elements in their standard states at 298.15 K and 101,325 Pa. These include C (graphite) and S (rhombic). Enthalpy of combus-
tion is the net value for the compound in its standard state at 298.15 K and 101,325 Pa. Products of combustion are taken to be CO2 (gas), H2O (gas), Cl2 (gas), Br2 (gas), I2 (gas), SO2 (gas),
N2 (gas), P4O10 (crystalline), SiO2 (crystobalite), and Al2O3 (crystal, alpha).
Values in this table were taken from the Design Institute for Physical Properties (DIPPR) of the American Institute of Chemical Engineers (AIChE), copyright 2007 AIChE and reproduced with permission of
AICHE and of the DIPPR Evaluated Process Design Data Project Steering Committee. Their source should be cited as R. L. Rowley, W. V. Wilding, J. L. Oscarson, Y. Yang, N. A. Zundel, T. E. Daubert, R. P. Dan-
ner, DIPPR® Data Compilation of Pure Chemical Properties, Design Institute for Physical Properties, AIChE, New York (2007).