Selected ATcT [1, 2] enthalpy of formation based on version 1.130 of the Thermochemical Network [3]

This version of ATcT results[4] was generated by additional expansion of version 1.128 [5,6] to include with the calculations provided in reference [4].

Hydrogen peroxide

Formula: HOOH (cr,l)
CAS RN: 7722-84-1
ATcT ID: 7722-84-1*500
SMILES: OO
InChI: InChI=1S/H2O2/c1-2/h1-2H
InChIKey: MHAJPDPJQMAIIY-UHFFFAOYSA-N
Hills Formula: H2O2

2D Image:

OO
Aliases: Hydrogen peroxide; Dioxidane; Dihydrogen peroxide; Hydrogen dioxide; Dihydrogen dioxide; Albone; Oxydol; Perhydrol; Superoxol; HOOH; H2O2
Relative Molecular Mass: 34.01468 ± 0.00062

   ΔfH°(0 K)   ΔfH°(298.15 K)UncertaintyUnits
-193.105-187.287± 0.077kJ/mol

Top contributors to the provenance of ΔfH° of HOOH (cr,l)

The 20 contributors listed below account only for 84.7% of the provenance of ΔfH° of HOOH (cr,l).
A total of 39 contributors would be needed to account for 90% of the provenance.

Please note: The list is limited to 20 most important contributors or, if less, a number sufficient to account for 90% of the provenance. The Reference acts as a further link to the relevant references and notes for the measurement. The Measured Quantity is normaly given in the original units; in cases where we have reinterpreted the original measurement, the listed value may differ from that given by the authors. The quoted uncertainty is the a priori uncertainty used as input when constructing the initial Thermochemical Network, and corresponds either to the value proposed by the original authors or to our estimate; if an additional multiplier is given in parentheses immediately after the prior uncertainty, it corresponds to the factor by which the prior uncertainty needed to be multiplied during the ATcT analysis in order to make that particular measurement consistent with the prevailing knowledge contained in the Thermochemical Network.

Contribution
(%)
TN
ID
Reaction Measured Quantity Reference
24.7237.9 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.925 ± 0.073 kJ/molScatchard 1952, 3rd Law, apud Gurvich TPIS
17.3240.1 HOOH (g) → 2 OH (g) ΔrH°(0 K) = 17051.8 ± 3.4 cm-1Luo 1992
8.2121.2 1/2 O2 (g) H2 (g) → H2O (cr,l) ΔrH°(298.15 K) = -285.8261 ± 0.040 kJ/molRossini 1939, Rossini 1931, Rossini 1931b, note H2Oa, Rossini 1930
5.8237.4 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.92 ± 0.15 kJ/molMaass 1924, 3rd Law, apud Gurvich TPIS
5.3236.3 HOOH (cr,l) → H2O (cr,l) + 1/2 O2 (g) ΔrH°(293.15 K) = -23.48 ± 0.03 (×2.229) kcal/molRoth 1930, est unc
5.1237.7 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.75 ± 0.16 kJ/molEgerton 1951, 3rd Law, apud Gurvich TPIS
4.0236.4 HOOH (cr,l) → H2O (cr,l) + 1/2 O2 (g) ΔrH°(293.15 K) = -23.47 ± 0.02 (×3.83) kcal/molMatheson 1929, est unc
2.42277.7 CH4 (g) + 2 O2 (g) → CO2 (g) + 2 H2O (cr,l) ΔrH°(298.15 K) = -890.578 ± 0.078 kJ/molSchley 2010
2.22279.1 H2 (g) C (graphite) → CH4 (g) ΔrG°(1165 K) = 37.521 ± 0.068 kJ/molSmith 1946, note COf, 3rd Law
2.1236.1 HOOH (cr,l) → H2O (cr,l) + 1/2 O2 (g) ΔrH°(300.05 K) = -23.44 ± 0.02 (×5.301) kcal/molGiguere 1955
0.7237.1 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.47 ± 0.40 (×1.044) kJ/molNBS Tables 1989
0.7238.3 HOOH (cr,l) → HOOH (g) ΔrH°(273.15 K) = 12.616 ± 0.1 kcal/molGiguere 1962, est unc
0.7238.4 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 12.337 ± 0.1 kcal/molGiguere 1962, est unc
0.7238.5 HOOH (cr,l) → HOOH (g) ΔrH°(318.15 K) = 12.119 ± 0.1 kcal/molGiguere 1962, est unc
0.7238.6 HOOH (cr,l) → HOOH (g) ΔrH°(333.15 K) = 11.949 ± 0.1 kcal/molGiguere 1962, est unc
0.7238.1 HOOH (cr,l) → HOOH (g) ΔrH°(300.05 K) = 12.315 ± 0.1 kcal/molGiguere 1955, note H2O2c
0.7238.2 HOOH (cr,l) → HOOH (g) ΔrH°(273.15 K) = 12.59 ± 0.1 kcal/molFoley 1951, note H2O2b
0.5111.11 H2O (g) → O (g) + 2 H (g) ΔrH°(0 K) = 917.80 ± 0.15 kJ/molThorpe 2021
0.5153.1 OH (g) → [OH]+ (g) ΔrH°(0 K) = 104989 ± 5 (×2.278) cm-1Wiedmann 1992, note unc
0.5221.4 HOOH (g) → 2 H (g) + 2 O (g) ΔrH°(0 K) = 1054.84 ± 0.56 kJ/molHarding 2008

Top 10 species with enthalpies of formation correlated to the ΔfH° of HOOH (cr,l)

Please note: The correlation coefficients are obtained by renormalizing the off-diagonal elements of the covariance matrix by the corresponding variances.
The correlation coefficient is a number from -1 to 1, with 1 representing perfectly correlated species, -1 representing perfectly anti-correlated species, and 0 representing perfectly uncorrelated species.


Correlation
Coefficent
(%)
Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass
ATcT ID
70.2 Hydrogen peroxideHOOH (g)OO-129.417-135.403± 0.058kJ/mol34.01468 ±
0.00062
7722-84-1*0
70.2 Hydrogen peroxideHOOH (g, para)OO-129.417-135.403± 0.058kJ/mol34.01468 ±
0.00062
7722-84-1*2
70.2 Hydrogen peroxideHOOH (g, ortho)OO-129.397-135.403± 0.058kJ/mol34.01468 ±
0.00062
7722-84-1*1
52.4 HydroxylOH (g)[OH]37.27937.518± 0.022kJ/mol17.00734 ±
0.00031
3352-57-6*0
52.4 Hydroxyde[OH]- (g)[OH-]-139.063-139.030± 0.022kJ/mol17.00789 ±
0.00031
14280-30-9*0
52.3 WaterH2O (g, ortho)O-238.617-241.805± 0.022kJ/mol18.01528 ±
0.00033
7732-18-5*1
52.3 WaterH2O (g, para)O-238.902-241.805± 0.022kJ/mol18.01528 ±
0.00033
7732-18-5*2
52.3 WaterH2O (g)O-238.902-241.805± 0.022kJ/mol18.01528 ±
0.00033
7732-18-5*0
52.3 WaterH2O (l, eq.press.)O-285.801± 0.022kJ/mol18.01528 ±
0.00033
7732-18-5*589
52.3 WaterH2O (l)O-285.800± 0.022kJ/mol18.01528 ±
0.00033
7732-18-5*590

Most Influential reactions involving HOOH (cr,l)

Please note: The list, which is based on a hat (projection) matrix analysis, is limited to no more than 20 largest influences.

Influence
Coefficient
TN
ID
Reaction Measured Quantity Reference
0.556237.9 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.925 ± 0.073 kJ/molScatchard 1952, 3rd Law, apud Gurvich TPIS
0.522239.3 HOOH (cr,l) → HOOH (aq) ΔrH°(298.15 K) = -3.39 ± 0.40 kJ/molNBS Tables 1989
0.477239.2 HOOH (cr,l) → HOOH (aq) ΔrH°(298.15 K) = -0.819 ± 0.100 kcal/molGiguere 1955, est unc
0.131237.4 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.92 ± 0.15 kJ/molMaass 1924, 3rd Law, apud Gurvich TPIS
0.115237.7 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.75 ± 0.16 kJ/molEgerton 1951, 3rd Law, apud Gurvich TPIS
0.058236.3 HOOH (cr,l) → H2O (cr,l) + 1/2 O2 (g) ΔrH°(293.15 K) = -23.48 ± 0.03 (×2.229) kcal/molRoth 1930, est unc
0.044236.4 HOOH (cr,l) → H2O (cr,l) + 1/2 O2 (g) ΔrH°(293.15 K) = -23.47 ± 0.02 (×3.83) kcal/molMatheson 1929, est unc
0.023236.1 HOOH (cr,l) → H2O (cr,l) + 1/2 O2 (g) ΔrH°(300.05 K) = -23.44 ± 0.02 (×5.301) kcal/molGiguere 1955
0.017237.1 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 51.47 ± 0.40 (×1.044) kJ/molNBS Tables 1989
0.016238.2 HOOH (cr,l) → HOOH (g) ΔrH°(273.15 K) = 12.59 ± 0.1 kcal/molFoley 1951, note H2O2b
0.016238.5 HOOH (cr,l) → HOOH (g) ΔrH°(318.15 K) = 12.119 ± 0.1 kcal/molGiguere 1962, est unc
0.016238.3 HOOH (cr,l) → HOOH (g) ΔrH°(273.15 K) = 12.616 ± 0.1 kcal/molGiguere 1962, est unc
0.016238.1 HOOH (cr,l) → HOOH (g) ΔrH°(300.05 K) = 12.315 ± 0.1 kcal/molGiguere 1955, note H2O2c
0.016238.6 HOOH (cr,l) → HOOH (g) ΔrH°(333.15 K) = 11.949 ± 0.1 kcal/molGiguere 1962, est unc
0.016238.4 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 12.337 ± 0.1 kcal/molGiguere 1962, est unc
0.000237.6 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 47.51 ± 3.1 (×1.414) kJ/molEgerton 1951, 2nd Law, apud Gurvich TPIS
0.000237.3 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 47.95 ± 4.4 kJ/molMaass 1924, 2nd Law, apud Gurvich TPIS
0.000237.8 HOOH (cr,l) → HOOH (g) ΔrH°(298.15 K) = 52.2 ± 10 kJ/molScatchard 1952, 2nd Law, apud Gurvich TPIS


References
1   B. Ruscic, R. E. Pinzon, M. L. Morton, G. von Laszewski, S. Bittner, S. G. Nijsure, K. A. Amin, M. Minkoff, and A. F. Wagner,
Introduction to Active Thermochemical Tables: Several "Key" Enthalpies of Formation Revisited.
J. Phys. Chem. A 108, 9979-9997 (2004) [DOI: 10.1021/jp047912y]
2   B. Ruscic, R. E. Pinzon, G. von Laszewski, D. Kodeboyina, A. Burcat, D. Leahy, D. Montoya, and A. F. Wagner,
Active Thermochemical Tables: Thermochemistry for the 21st Century.
J. Phys. Conf. Ser. 16, 561-570 (2005) [DOI: 10.1088/1742-6596/16/1/078]
3   B. Ruscic and D. H. Bross,
Active Thermochemical Tables (ATcT) values based on ver. 1.130 of the Thermochemical Network. Argonne National Laboratory, Lemont, Illinois 2023; available at ATcT.anl.gov
[DOI: 10.17038/CSE/1997229]
4   N. Genossar, P. B. Changala, B. Gans, J.-C. Loison, S. Hartweg, M.-A. Martin-Drumel, G. A. Garcia, J. F. Stanton, B. Ruscic, and J. H. Baraban
Ring-Opening Dynamics of the Cyclopropyl Radical and Cation: the Transition State Nature of the Cyclopropyl Cation
J. Am. Chem. Soc. 144, 18518-18525 (2022) [DOI: 10.1021/jacs.2c07740]
5   B. Ruscic and D. H. Bross
Active Thermochemical Tables: The Thermophysical and Thermochemical Properties of Methyl, CH3, and Methylene, CH2, Corrected for Nonrigid Rotor and Anharmonic Oscillator Effects.
Mol. Phys. e1969046 (2021) [DOI: 10.1080/00268976.2021.1969046]
6   J. H. Thorpe, J. L. Kilburn, D. Feller, P. B. Changala, D. H. Bross, B. Ruscic, and J. F. Stanton,
Elaborated Thermochemical Treatment of HF, CO, N2, and H2O: Insight into HEAT and Its Extensions
J. Chem. Phys. 155, 184109 (2021) [DOI: 10.1063/5.0069322]
7   B. Ruscic,
Uncertainty Quantification in Thermochemistry, Benchmarking Electronic Structure Computations, and Active Thermochemical Tables.
Int. J. Quantum Chem. 114, 1097-1101 (2014) [DOI: 10.1002/qua.24605]
8   B. Ruscic and D. H. Bross,
Thermochemistry
Computer Aided Chem. Eng. 45, 3-114 (2019) [DOI: 10.1016/B978-0-444-64087-1.00001-2]

Formula
The aggregate state is given in parentheses following the formula, such as: g - gas-phase, cr - crystal, l - liquid, etc.

Uncertainties
The listed uncertainties correspond to estimated 95% confidence limits, as customary in thermochemistry (see, for example, Ruscic [6]).
Note that an uncertainty of ± 0.000 kJ/mol indicates that the estimated uncertainty is < ± 0.0005 kJ/mol.

Website Functionality Credits
The reorganization of the website was developed and implemented by David H. Bross (ANL).
The find function is based on the complete Species Dictionary entries for the appropriate version of the ATcT TN.
The molecule images are rendered by Indigo-depict.
The XYZ renderings are based on Jmol: an open-source Java viewer for chemical structures in 3D. http://www.jmol.org/.

Acknowledgement
This work was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences and Biosciences under Contract No. DE-AC02-06CH11357.