Formaldehyde

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Gas phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
GT - Glushko Thermocenter, Russian Academy of Sciences, Moscow

Quantity Value Units Method Reference Comment
Δfgas-27.701kcal/molReviewChase, 1998Data last reviewed in March, 1961
Δfgas-25.95 ± 0.11kcal/molCmFletcher and Pilcher, 1970ALS
Quantity Value Units Method Reference Comment
Δcgas-136.42 ± 0.10kcal/molCmFletcher and Pilcher, 1970Corresponding Δfgas = -25.95 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS
Δcgas-134.1kcal/molCcbWartenberg and Lerner-Steinberg, 1925Gas phase; Corresponding Δfgas = -28.3 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS
Quantity Value Units Method Reference Comment
gas,1 bar52.330cal/mol*KReviewChase, 1998Data last reviewed in March, 1961

Constant pressure heat capacity of gas

Cp,gas (cal/mol*K) Temperature (K) Reference Comment
7.94950.Thermodynamics Research Center, 1997p=1 bar. Recommended entropies and heat capacities are in good agreement with other statistically calculated values [ Thompson, 1941, Pillai M.G.K., 1961, Gurvich, Veyts, et al., 1989]. Please also see Chao J., 1980, Chao J., 1986.; GT
7.949100.
7.954150.
8.007200.
8.293273.15
8.458 ± 0.005298.15
8.470300.
9.379400.
10.45500.
11.52600.
12.50700.
13.37800.
14.14900.
14.811000.
15.381100.
15.881200.
16.311300.
16.681400.
17.011500.
17.641750.
18.092000.
18.422250.
18.672500.
18.862750.
19.023000.

Gas Phase Heat Capacity (Shomate Equation)

Cp° = A + B*t + C*t2 + D*t3 + E/t2
H° − H°298.15= A*t + B*t2/2 + C*t3/3 + D*t4/4 − E/t + F − H
S° = A*ln(t) + B*t + C*t2/2 + D*t3/3 − E/(2*t2) + G
    Cp = heat capacity (cal/mol*K)
    H° = standard enthalpy (kcal/mol)
    S° = standard entropy (cal/mol*K)
    t = temperature (K) / 1000.

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Temperature (K) 298. to 1200.1200. to 6000.
A 1.24134117.05370
B 22.283101.475740
C -10.72050-0.284677
D 1.8839100.019016
E 0.131734-3.725902
F -28.52751-40.78219
G 48.3906162.69551
H -27.70010-27.70010
ReferenceChase, 1998Chase, 1998
Comment Data last reviewed in March, 1961 Data last reviewed in March, 1961

References

Go To: Top, Gas phase thermochemistry data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Chase, 1998
Chase, M.W., Jr., NIST-JANAF Themochemical Tables, Fourth Edition, J. Phys. Chem. Ref. Data, Monograph 9, 1998, 1-1951. [all data]

Fletcher and Pilcher, 1970
Fletcher, R.A.; Pilcher, G., Measurements of heats of combustion by flame calorimetry, Trans. Faraday Soc., 1970, 66, 794-799. [all data]

Wartenberg and Lerner-Steinberg, 1925
Wartenberg, H.; Lerner-Steinberg, Heat of formation of formaldehyde, Z. Angew. Chem., 1925, 38, 591-592. [all data]

Thermodynamics Research Center, 1997
Thermodynamics Research Center, Selected Values of Properties of Chemical Compounds., Thermodynamics Research Center, Texas A&M University, College Station, Texas, 1997. [all data]

Thompson, 1941
Thompson, H.W., Thermodynamic functions and equilibria of formaldehyde, deuteroformaldehyde, phosgene and thiophosgene, Trans. Faraday Soc., 1941, 37, 251-260. [all data]

Pillai M.G.K., 1961
Pillai M.G.K., Potential energy constants, rotational distortion constants, and calculated thermodynamic properties for some planar XYZ2 molecules, J. Mol. Spectrosc., 1961, 6, 465-471. [all data]

Gurvich, Veyts, et al., 1989
Gurvich, L.V.; Veyts, I.V.; Alcock, C.B., Thermodynamic Properties of Individual Substances, 4th ed.; Vols. 1 and 2, Hemisphere, New York, 1989. [all data]

Chao J., 1980
Chao J., Perfect gas thermodynamic properties of methanal, ethanal and their deuterated species, Thermochim. Acta, 1980, 41, 41-54. [all data]

Chao J., 1986
Chao J., Thermodynamic properties of key organic oxygen compounds in the carbon range C1 to C4. Part 2. Ideal gas properties, J. Phys. Chem. Ref. Data, 1986, 15, 1369-1436. [all data]


Notes

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