Kinetics of COx formation in the homogeneous metal/bromide-catalyzed aerobic oxidation of p-xylene
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作者:
Sun, Weizhen
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E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R ChinaE China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
Sun, Weizhen
[1
]
An, Meiying
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E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R ChinaE China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
An, Meiying
[1
]
Zhong, Weimin
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E China Univ Sci & Technol, Key Lab Adv Control & Optimizat Chem Proc, Minist Educ, Shanghai 200237, Peoples R ChinaE China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
Zhong, Weimin
[2
]
Zhao, Ling
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E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R ChinaE China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
Zhao, Ling
[1
]
机构:
[1] E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] E China Univ Sci & Technol, Key Lab Adv Control & Optimizat Chem Proc, Minist Educ, Shanghai 200237, Peoples R China
The homogeneous metal/bromide-catalyzed aerobic oxidation of p-xylene with different catalyst concentrations was carried out, and the formation kinetics of COx including CO2 and CO was measured. The simplified elementary steps for the formation of COx were summarized, on the basis of which the kinetic model of COx formation was established. The model calculations were in good agreement with the experimental data for the CO2 formation and also successfully captured the first peak of the CO formation rate as a function of time. The obtained rate constants have narrow confidence intervals, among which only k1 and k2 are the adjustable parameters for different catalyst conditions. The decarboxylation of the carboxyl group in aromatic acid, the oxidation of the aryl radical, and the destruction of acetic acid are the major sources of CO2. The formation of CO mainly results from the destruction of acetic acid and the oxidation of the aryl radical. (C) 2012 Wiley Periodicals, Inc. Int J Chem Kinet 44: 277283, 2012
机构:
EI DuPont Nemours & Co inc, Expt Stn, Cent Res & Dev, Wilmington, DE 19880 USAEI DuPont Nemours & Co inc, Expt Stn, Cent Res & Dev, Wilmington, DE 19880 USA
机构:
Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Williams, C. Luke
Vinter, Katherine P.
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Univ Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Vinter, Katherine P.
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Chang, Chun-Chih
Xiong, Ruichang
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Univ Delaware, Dept Chem & Biomol Engn, Colburn Lab, Newark, DE 19716 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Xiong, Ruichang
Green, Sara K.
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Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Green, Sara K.
Sandler, Stanley I.
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Univ Delaware, Dept Chem & Biomol Engn, Colburn Lab, Newark, DE 19716 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Sandler, Stanley I.
Vlachos, Dionisios G.
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Univ Delaware, Dept Chem & Biomol Engn, Colburn Lab, Newark, DE 19716 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Vlachos, Dionisios G.
Fan, Wei
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Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
Fan, Wei
Dauenhauer, Paul J.
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Univ Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
US DOE, Catalysis Ctr Energy Innovat, Frontier Res Ctr, Washington, DC 20585 USAUniv Minnesota, Dept Chem Engn Mat Sci, Minneapolis, MN 55455 USA
机构:
EI DuPont de Nemours & Co Inc, Cent Res & Dev, Expt Stn, Wilmington, DE 19880 USAEI DuPont de Nemours & Co Inc, Cent Res & Dev, Expt Stn, Wilmington, DE 19880 USA
机构:
East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R ChinaEast China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
Lyu, Quanming
Dong, Jian
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East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R ChinaEast China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
Dong, Jian
He, Renchu
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East China Univ Sci & Technol, Key Lab Adv Control & Optimizat Chem Proc, Minist Educ, Shanghai 200237, Peoples R ChinaEast China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
He, Renchu
Sun, Weizhen
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East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R ChinaEast China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
Sun, Weizhen
Zhao, Ling
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East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
XinJiang Univ, Sch Chem & Chem Engn, Urumqi 830046, Peoples R ChinaEast China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China