Oxygen
- Formula: O2
- Molecular weight: 31.9988
- IUPAC Standard InChIKey: MYMOFIZGZYHOMD-UHFFFAOYSA-N
- CAS Registry Number: 7782-44-7
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Molecular oxygen; Oxygen molecule; Pure oxygen; O2; Liquid oxygen; UN 1072; UN 1073; Dioxygen
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
- Data at other public NIST sites:
- Options:
Data at NIST subscription sites:
- NIST / TRC Web Thermo Tables, "lite" edition (thermophysical and thermochemical data)
- NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)
NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.
Phase change data
Go To: Top, Reaction thermochemistry data, References, Notes
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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 90.2 | K | N/A | Streng, 1971 | Uncertainty assigned by TRC = 0.2 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 54.8 | K | N/A | Streng, 1971 | Uncertainty assigned by TRC = 0.2 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Ttriple | 54.33 | K | N/A | Henning and Otto, 1936 | Uncertainty assigned by TRC = 0.06 K; temperature measured with He gas thermometer; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Tc | 154.58 | K | N/A | Pentermann and Wagner, 1978 | Uncertainty assigned by TRC = 0.0015 K; TRC |
Tc | 154.58 | K | N/A | Wagner, Ewers, et al., 1976 | Uncertainty assigned by TRC = 0.0015 K; TRC |
Tc | 155.15 | K | N/A | Cardoso, 1915 | Uncertainty assigned by TRC = 0.3 K; 4 determinations with same result; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Pc | 50.43 | bar | N/A | Wagner, Ewers, et al., 1976 | Uncertainty assigned by TRC = 0.005 bar; Vapour-pressure measurements give pc=5.04332 MPa at Tc from L.A.Weber, 1970 PRT, IPTS-68, PP+ differential pressure transducer.; TRC |
Pc | 50.0343 | bar | N/A | Cardoso, 1915 | Uncertainty assigned by TRC = 0.3039 bar; TRC |
Pc | 49.9228 | bar | N/A | Cardoso, 1915 | Uncertainty assigned by TRC = 0.3039 bar; TRC |
Pc | 49.8519 | bar | N/A | Cardoso, 1915 | Uncertainty assigned by TRC = 0.3039 bar; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ρc | 13.60 | mol/l | N/A | Pentermann and Wagner, 1978 | Uncertainty assigned by TRC = 0.014 mol/l; from density measurements 65 to 300 K, Tc from Weber, 1970; TRC |
Antoine Equation Parameters
log10(P) = A − (B / (T + C))
P = vapor pressure (bar)
T = temperature (K)
View plot Requires a JavaScript / HTML 5 canvas capable browser.
Temperature (K) | A | B | C | Reference | Comment |
---|---|---|---|---|---|
54.36 to 100.16 | 3.85845 | 325.675 | -5.667 | Brower and Thodos, 1968 | Coefficents calculated by NIST from author's data. |
54.36 to 154.33 | 3.9523 | 340.024 | -4.144 | Brower and Thodos, 1968 | Coefficents calculated by NIST from author's data. |
Reaction thermochemistry data
Go To: Top, Phase change data, References, Notes
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:
B - John E. Bartmess
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.
Reactions 1 to 50
By formula: O2- + O2 = (O2- • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 48. ± 20. | kJ/mol | AVG | N/A | Average of 5 out of 7 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 102. | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 130. | J/mol*K | PHPMS | Conway and Nesbit, 1968 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 13. ± 4.6 | kJ/mol | TDAs | Hiraoka, 1888 | gas phase; see also Sherwood, Hanold, et al., 1996. Aquino, Taylor, et al., 2001 calns indicate rectangular anion; B |
ΔrG° | 23. ± 4.2 | kJ/mol | IMRE | Payzant J.D. and Kebarle, 1972 | gas phase; B |
ΔrG° | 13. ± 4.2 | kJ/mol | IMRE | Pack and Phelps, 1971 | gas phase; B |
ΔrG° | 16.7 ± 2.1 | kJ/mol | IMRE | Parkes, 1971 | gas phase; B |
ΔrG° | 16. ± 4.2 | kJ/mol | TDAs | Conway and Nesbit, 1968 | gas phase; B |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
15. | 300. | DT | Pack and Phelps, 1971 | gas phase; M |
By formula: O2+ + O2 = (O2+ • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 41. ± 5. | kJ/mol | AVG | N/A | Average of 5 out of 6 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.7 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 104.7 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase; M |
ΔrS° | 84. | J/mol*K | PHPMS | Durden, Kebarle, et al., 1969 | gas phase; M |
ΔrS° | 86.2 | J/mol*K | PHPMS | Yang and Conway, 1964 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
16. | 300. | DT | Rakshit and Warneck, 1981 | gas phase; M |
14. | 300. | DT | Rakshit and Warneck, 1980 | gas phase; M |
14. | 296. | FA | Howard, Bierbaum, et al., 1972 | gas phase; M |
25. | 200. | FA | Adams and Bohme, 1970 | gas phase; M |
By formula: (HO2+ • 2O2) + O2 = (HO2+ • 3O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrH° | 13. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 76.6 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrS° | 84. | J/mol*K | N/A | Hiraoka, Saluja, et al., 1979 | gas phase; Entropy change calculated or estimated; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
4.6 | 105. | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; Entropy change calculated or estimated; M |
By formula: (O2- • 7N2 • O2) + N2 = (O2- • 8N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
ΔrH° | 6.40 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 74.9 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
ΔrS° | 75.3 | J/mol*K | N/A | Hiraoka, 1988, 2 | gas phase; Entropy change calculated or estimated; M |
By formula: O- + O2 = (O- • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 130. | kJ/mol | PDiss | Hiller and Vestal, 1981 | gas phase; From thermochemical cycle, ΔrH<; M |
ΔrH° | 163. | kJ/mol | PES | Novich, Engelking, et al., 1979 | gas phase; From thermochemical cycle, from EA(O3), D(O-O2) AND EA(O); M |
ΔrH° | 160. | kJ/mol | PDiss | Cosby, Moseley, et al., 1978 | gas phase; M |
ΔrH° | 180. | kJ/mol | CID | Lifschitz, Wu, et al., 1978 | gas phase; M |
By formula: (O2+ • O2) + O2 = (O2+ • 2O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 25. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrH° | 28.7 ± 0.3 | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 110. | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 133.0 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase; M |
By formula: (HO2+ • O2) + O2 = (HO2+ • 2O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 29. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrH° | 28. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 96.7 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrS° | 92. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
By formula: (O2+ • 3O2) + O2 = (O2+ • 4O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrH° | 10.3 ± 0.75 | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 88.7 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 100. | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase; M |
By formula: (O2+ • 2O2) + O2 = (O2+ • 3O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.4 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrH° | 10.6 ± 0.4 | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.2 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 82.8 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase; M |
By formula: (O2+ • 4O2) + O2 = (O2+ • 5O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrH° | 8. ± 3. | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 89.5 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 71.1 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase; M |
By formula: O3- + O2 = (O3- • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8.79 ± 0.84 | kJ/mol | TDAs | Hiraoka, 1988, 2 | gas phase; B,M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 79.5 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | -15.1 ± 2.1 | kJ/mol | TDAs | Hiraoka, 1988, 2 | gas phase; B |
By formula: NO- + O2 = (NO- • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12.1 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 60.7 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
-2. | 200. | FA | Dunkin, Fehsenfeld, et al., 1971 | gas phase; DG>; M |
By formula: (O2- • 6O2) + O2 = (O2- • 7O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 5.86 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67. | J/mol*K | N/A | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated; M |
By formula: (O2+ • 7O2) + O2 = (O2+ • 8O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.61 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | N/A | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated; M |
By formula: (O2+ • O2) + N2 = (O2+ • N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 42.3 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
By formula: (H3+ • O2) + O2 = (H3+ • 2O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 48.1 | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; From thermochemical cycle(O2H+)O2; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; From thermochemical cycle(O2H+)O2; M |
By formula: (O3- • 4O2) + O2 = (O3- • 5O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6.44 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; ΔrH, ΔrS approximate; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 68.6 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; ΔrH, ΔrS approximate; M |
By formula: H3+ + O2 = (H3+ • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 52.3 | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; From thermochemical cycle(O2H+)O2; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 82.0 | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; From thermochemical cycle(O2H+)O2; M |
(O2S- • 2 • ) + = (O2S- • 3 • )
By formula: (O2S- • 2O2S • O2) + O2S = (O2S- • 3O2S • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 15.1 ± 1.7 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 6. ± 13. | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
By formula: (O2S- • O2S • O2) + O2S = (O2S- • 2O2S • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 19.2 ± 1.7 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 10. ± 8.4 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
By formula: (O3S- • O2S • O2) + O2S = (O3S- • 2O2S • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 23.8 ± 2.5 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 15. ± 8.8 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
By formula: O+ + O2 = (O+ • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 179. | kJ/mol | PDiss | Hiller and Vestal, 1982 | gas phase; M |
ΔrH° | 200. | kJ/mol | PI | Linn, Ono, et al., 1981 | gas phase; M |
ΔrH° | 209. | kJ/mol | PDiss | Mosely, Ozenne, et al., 1981 | gas phase; M |
By formula: (O3S- • O2) + O2S = (O3S- • O2S • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 27.2 ± 3.3 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 18. ± 9.2 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
By formula: (O2S- • O2) + O2S = (O2S- • O2S • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 46.0 ± 4.2 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 26. ± 9.2 | kJ/mol | TDAs | Vacher, Jorda, et al., 1992 | gas phase; B |
By formula: (O2- • 2N2 • O2) + N2 = (O2- • 3N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.3 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 76.6 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: (O2- • 3N2 • O2) + N2 = (O2- • 4N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.2 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: (O2- • 4N2 • O2) + N2 = (O2- • 5N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8.1 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 81.6 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: (O2- • 5N2 • O2) + N2 = (O2- • 6N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.6 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 81.6 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: (O2- • 6N2 • O2) + N2 = (O2- • 7N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.1 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.7 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: (O2- • N2 • O2) + N2 = (O2- • 2N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.7 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 74.9 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: (NO- • 2O2) + O2 = (NO- • 3O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.8 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 65.7 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
By formula: (NO- • 3O2) + O2 = (NO- • 4O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.2 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67.4 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
By formula: (NO- • 4O2) + O2 = (NO- • 5O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9.8 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 80.3 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
By formula: (NO- • O2) + O2 = (NO- • 2O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12.1 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 65.7 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1991 | gas phase; M |
By formula: (HO2+ • 3O2) + O2 = (HO2+ • 4O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 88.3 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (HO2+ • 4O2) + O2 = (HO2+ • 5O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 91.6 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (HO2+ • 5O2) + O2 = (HO2+ • 6O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 93.3 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (HO2+ • 6O2) + O2 = (HO2+ • 7O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 94.1 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (HO2+ • 7O2) + O2 = (HO2+ • 8O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 88.3 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (HO2+ • 8O2) + O2 = (HO2+ • 9O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 86.2 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (HO2+ • O2) + H2 = (HO2+ • H2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 17. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 71. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
By formula: (O2- • O2) + N2 = (O2- • N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 69.0 | J/mol*K | PHPMS | Hiraoka, 1988, 2 | gas phase; M |
By formula: 2C2H6S + O2 = 2C2H6OS
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -277.7 ± 0.84 | kJ/mol | Cm | Douglas, 1946 | liquid phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -278.3 ± 0.8 kJ/mol; At 291°K; ALS |
By formula: C2H6O2S = C2H6OS + 0.5O2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 243.3 ± 0.84 | kJ/mol | Cm | Douglas, 1946 | liquid phase; Reanalyzed by Cox and Pilcher, 1970, Original value = 246.9 ± 0.8 kJ/mol; At 291°K; ALS |
By formula: (O2- • 2O2) + O2 = (O2- • 3O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 89.1 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 3O2) + O2 = (O2- • 4O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 64.4 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 4O2) + O2 = (O2- • 5O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6.4 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 64.4 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 5O2) + O2 = (O2- • 6O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67.8 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2+ • 5O2) + O2 = (O2+ • 6O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 90.8 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2+ • 6O2) + O2 = (O2+ • 7O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 2. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 91.6 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
References
Go To: Top, Phase change data, Reaction thermochemistry data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Streng, 1971
Streng, A.G.,
Miscibility and Compatibility of Some Liquid and Solidified Gases at Low Temperature,
J. Chem. Eng. Data, 1971, 16, 357. [all data]
Henning and Otto, 1936
Henning, F.; Otto, J.,
Vapor pressure curves and triple points in the temperature region from 14 to 90 k,
Phys. Z., 1936, 37, 633-8. [all data]
Pentermann and Wagner, 1978
Pentermann, W.; Wagner, W.,
New pressure-density-temperature measurements and new rational equations for the saturated liquid and vapor densities of oxygen,
J. Chem. Thermodyn., 1978, 10, 1161-1172. [all data]
Wagner, Ewers, et al., 1976
Wagner, W.; Ewers, J.; Pentermann, W.,
A New Vapor-Pressure Measurement and a New Rational Vapor-Pressure Equation for Oxygen,
J. Chem. Thermodyn., 1976, 8, 1049. [all data]
Cardoso, 1915
Cardoso, E.,
Study of the Critical Point of Several Difficultly LIquifiable Gases: Nitrogen, Carbon Monoxide, Oxygen and Methane,
J. Chim. Phys. Phys.-Chim. Biol., 1915, 13, 312. [all data]
Brower and Thodos, 1968
Brower, G.T.; Thodos, G.,
Vapor Pressures of Liquid Oxygen Between the Triple Point and Critical Point,
J. Chem. Eng. Data, 1968, 13, 2, 262-264, https://doi.org/10.1021/je60037a038
. [all data]
Hiraoka, 1988
Hiraoka, K.,
A Determination of the Stabilities of O2+(O2)n and O2-(O2)n with n = 1 - 8 from Measurements of the Gas-Phase Ion Equilibria,
J. Chem. Phys., 1988, 89, 5, 3190, https://doi.org/10.1063/1.454976
. [all data]
Conway and Nesbit, 1968
Conway, D.C.; Nesbit, L.E.,
Stability of O4-,
J. Chem. Phys., 1968, 48, 1, 509, https://doi.org/10.1063/1.1667956
. [all data]
Hiraoka, 1888
Hiraoka, K.,
A Determination of the Stability of O2+(O2)n and O2-(O2)n with n=1-8 from Measurements of the Gas Phase Ion Equilibria,
J. Chem. Phys., 1888, 89, 5, 3190, https://doi.org/10.1063/1.454976
. [all data]
Sherwood, Hanold, et al., 1996
Sherwood, C.R.; Hanold, K.A.; Garner, M.C.; Strong, K.M.; Continetti, R.E.,
Translational Spectroscopy Studies of the Photodissociation Dynamics of O4-,
J. Chem. Phys., 1996, 105, 24, 10803, https://doi.org/10.1063/1.472888
. [all data]
Aquino, Taylor, et al., 2001
Aquino, A.J.A.; Taylor, P.R.; Walch, S.P.,
Structure, properties, and photodissociation of O-4(-),
J. Chem. Phys., 2001, 114, 7, 3010-3017, https://doi.org/10.1063/1.1288379
. [all data]
Payzant J.D. and Kebarle, 1972
Payzant J.D.; Kebarle, P.,
Kinetics and Reactions Leading to O2-(H2O)n in Moist Oxygen,
J. Chem. Phys., 1972, 56, 7, 3482, https://doi.org/10.1063/1.1677723
. [all data]
Pack and Phelps, 1971
Pack, J.L.; Phelps, A.V.,
Hydration of Oxygen Negative Ions,
Bull. Am. Phys. Soc., 1971, 16, 214. [all data]
Parkes, 1971
Parkes, D.A.,
Electron Attachment and Negative Ion-Molecule Reactions in Pure O2,
Trans. Farad. Soc., 1971, 97, 711, https://doi.org/10.1039/tf9716700711
. [all data]
Conway and Janik, 1970
Conway, D.C.; Janik, G.S.,
Determination of the Bond Energies for the Series O2 - O2+ through O2 - O10+,
J. Chem. Phys., 1970, 53, 5, 1859, https://doi.org/10.1063/1.1674262
. [all data]
Durden, Kebarle, et al., 1969
Durden, D.A.; Kebarle, P.; Good, A.,
Thermal Ion-Molecule Reaction Rate Constants at Pressures up to 10 torr with a Pulsed Mass Spectrometer. Reactions in Methane, Krypton, and Oxygen,
J. Chem. Phys., 1969, 50, 2, 805, https://doi.org/10.1063/1.1671133
. [all data]
Yang and Conway, 1964
Yang, J.H.; Conway, D.C.,
Bonding in Ion Clusters. I. O4+,
J. Chem. Phys., 1964, 40, 6, 1729, https://doi.org/10.1063/1.1725389
. [all data]
Rakshit and Warneck, 1981
Rakshit, A.B.; Warneck, P.,
Formation and Reactions of O2+.CO2, O2+.H2O and O2+(CO2)2 Ions,
Int. J. Mass Spectrom Ion Phys., 1981, 40, 2, 135, https://doi.org/10.1016/0020-7381(81)80037-X
. [all data]
Rakshit and Warneck, 1980
Rakshit, A.B.; Warneck, P.,
A Drift Chamber Study of the Formation of Water Cluster Ions in Oxygen,
J. Chem. Phys., 1980, 73, 10, 5074, https://doi.org/10.1063/1.439985
. [all data]
Howard, Bierbaum, et al., 1972
Howard, C.J.; Bierbaum, V.M.; Rundle, H.W.; Kaufman, F.,
Kinetics and Mechanism of Formation of Water Cluster Ions from O2+ and H2O+,
J. Chem. Phys., 1972, 57, 8, 3491, https://doi.org/10.1063/1.1678783
. [all data]
Adams and Bohme, 1970
Adams, N.G.; Bohme, D.,
Flowing Afterglow Studies of Formation and Reactions of Cluster Ions of O2+, O2-, and O-,
J. Chem. Phys., 1970, 52, 6, 3133, https://doi.org/10.1063/1.1673449
. [all data]
Hiraoka and Mori, 1989
Hiraoka, K.; Mori, T.,
Gas Phase Stabilities of the Cluster Ions H+(CO)2(CO)n, H+(N2)2(N2)n and H+(O2)2(O2)n with n = 1 - 14,
Chem. Phys., 1989, 137, 1-3, 345, https://doi.org/10.1016/0301-0104(89)87119-8
. [all data]
Hiraoka, Saluja, et al., 1979
Hiraoka, K.; Saluja, P.P.S.; Kebarle, P.,
Stabilities of Complexes (N2)nH+, (CO)nH+ and (O2)nH+ for n = 1 to 7 Based on Gas Phase Ion Equilibrium Measurements,
Can. J. Chem., 1979, 57, 16, 2159, https://doi.org/10.1139/v79-346
. [all data]
Hiraoka, 1988, 2
Hiraoka, K.,
Determination of the Stabilities of O3-(N2)n, O3-(O2)n, and O4-(N2)n from Measurements of the Gas Phase Equilibria,
Chem. Phys., 1988, 125, 2-3, 439, https://doi.org/10.1016/0301-0104(88)87096-4
. [all data]
Hiller and Vestal, 1981
Hiller, J.F.; Vestal, M.L.,
Laser Photodissociation of O3- by Triple Quadrupole Mass Spectrometry,
J. Chem. Phys., 1981, 74, 11, 6096, https://doi.org/10.1063/1.441053
. [all data]
Novich, Engelking, et al., 1979
Novich, S.E.; Engelking, P.C.; Jones, P.L.; Futrell, J.H.; Lineberger, W.C.,
Laser photoelectron, photodetachment, and photodestruction spectra of O3-,
J. Chem. Phys., 1979, 70, 2652. [all data]
Cosby, Moseley, et al., 1978
Cosby, P.C.; Moseley, J.T.; Peterson, J.R.; Ling, J.H.,
Photodissociation spectroscopy of O3,
J. Chem. Phys., 1978, 69, 2771. [all data]
Lifschitz, Wu, et al., 1978
Lifschitz, C.; Wu, R.L.C.; Tiernan, T.O.; Terwillinger, D.T.,
Negative Ion - Molecule Reactions of Ozone and Their Implications on the Thermochemistry of O3-,
J. Chem. Phys., 1978, 68, 1, 247, https://doi.org/10.1063/1.435489
. [all data]
Hiraoka and Yamabe, 1991
Hiraoka, K.; Yamabe, S.,
Cluster Ions: Gas Phase Stabilities of NO+(O2)n and NO+(CO2)n with n = 1 - 5,
J. Chem. Phys., 1991, 95, 9, 6800, https://doi.org/10.1063/1.461518
. [all data]
Dunkin, Fehsenfeld, et al., 1971
Dunkin, D.B.; Fehsenfeld, F.C.; Schelmetekopf, A.L.; Ferguson, E.E.,
Three-Body Association Reactions of NO+ with O2, N2, and CO2,
J. Chem. Phys., 1971, 54, 9, 3817, https://doi.org/10.1063/1.1675432
. [all data]
Speller and Fitaire, 1983
Speller, C.V.; Fitaire, M.,
Proceedings of the 16th International Conference on Phenomena of Ionized Gases, H. Boetticher, H. Wenk and E. Shulz - Gulde, ed(s)., ICPIG, Dusseldorf, 1983, 568. [all data]
Vacher, Jorda, et al., 1992
Vacher, J.R.; Jorda, M.; Leduc, E.; Fitaire, M.,
A Determination of the Stabilities of Negative Ion Clusters in SO2 and SO2-O2 Mixtures,
Int. J. Mass Spectrom. Ion Proc., 1992, 114, 3, 149, https://doi.org/10.1016/0168-1176(92)80033-W
. [all data]
Hiller and Vestal, 1982
Hiller, J.F.; Vestal, M.L.,
Laser Photodissociation of O3+ and the Energetics of Ozone and its Ions,
J. Chem. Phys., 1982, 77, 3, 1248, https://doi.org/10.1063/1.444000
. [all data]
Linn, Ono, et al., 1981
Linn, S.H.; Ono, Y.; Ng, C.Y.,
A Study of the Ion - Molecule Half Reactions O2+(a4piu, v)...(O2)m ---> O2m+1 + O, m=1, 2, 3, Using the Molecular Beam Photoionization Method,
J. Chem. Phys., 1981, 74, 6, 3348, https://doi.org/10.1063/1.441487
. [all data]
Mosely, Ozenne, et al., 1981
Mosely, J.T.; Ozenne, J.B.; Cosby, P.C.,
Photofragment Spectroscopy of O3+,
J. Chem. Phys., 1981, 74, 1, 337, https://doi.org/10.1063/1.440839
. [all data]
Douglas, 1946
Douglas, T.B.,
Heats of formation of liquid methyl sulfoxide and crystalline methyl sulfone at 18°,
J. Am. Chem. Soc., 1946, 68, 1072-1076. [all data]
Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G.,
Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]
Notes
Go To: Top, Phase change data, Reaction thermochemistry data, References
- Symbols used in this document:
Pc Critical pressure T Temperature Tboil Boiling point Tc Critical temperature Tfus Fusion (melting) point Ttriple Triple point temperature ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔrS° Entropy of reaction at standard conditions ρc Critical density - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
- Customer support for NIST Standard Reference Data products.