Tunable catalytic properties of bi-functional mixed oxides in ethanol conversion to high value compounds
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作者:
Ramasamy, Karthikeyan K.
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Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USAPacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
Ramasamy, Karthikeyan K.
[1
]
Gray, Michel
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Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USAPacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
Gray, Michel
[1
]
Job, Heather
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Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USAPacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
Job, Heather
[1
]
Smith, Colin
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Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USAPacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
Smith, Colin
[1
]
Wang, Yong
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Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
Washington State Univ, Gene & Linda Voiland Sch Chem Engn & Bioengn, Pullman, WA 99164 USAPacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
Wang, Yong
[1
,2
]
机构:
[1] Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99354 USA
[2] Washington State Univ, Gene & Linda Voiland Sch Chem Engn & Bioengn, Pullman, WA 99164 USA
A highly versatile ethanol conversion process to selectively generate high value compounds is presented here. By changing the reaction temperature, ethanol can be selectively converted to >C-2 alcohols/oxygenates or phenolic compounds over hydrotalcite derived bi-functional MgO-Al2O3 catalyst via complex cascade mechanism. Reaction temperature plays a role in whether aldol condensation or the acetone formation is the path taken in changing the product composition. This article contains the catalytic activity comparison between the mono-functional and physical mixture counterpart to the hydrotalcite derived mixed oxides and the detailed discussion on the reaction mechanisms. (C) 2016 Published by Elsevier B.V.
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Inst Mil Engn, BR-22290270 Rio De Janeiro, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
Carvalho, Debora L.
;
de Avillez, Roberto R.
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Pontificia Univ Catolica Rio de Janeiro, BR-22453900 Rio De Janeiro, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
de Avillez, Roberto R.
;
Rodrigues, Michelly T.
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Inst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
Rodrigues, Michelly T.
;
Borges, Luiz E. P.
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Inst Mil Engn, BR-22290270 Rio De Janeiro, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
Borges, Luiz E. P.
;
Appel, Lucia G.
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Inst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
机构:
Inst Mil Engn, BR-22290270 Rio De Janeiro, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
Carvalho, Debora L.
;
de Avillez, Roberto R.
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机构:
Pontificia Univ Catolica Rio de Janeiro, BR-22453900 Rio De Janeiro, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
de Avillez, Roberto R.
;
Rodrigues, Michelly T.
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Inst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
Rodrigues, Michelly T.
;
Borges, Luiz E. P.
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Inst Mil Engn, BR-22290270 Rio De Janeiro, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil
Borges, Luiz E. P.
;
Appel, Lucia G.
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h-index: 0
机构:
Inst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, BrazilInst Nacl Tecnol, Div Catalise & Proc Quim, BR-21081312 Rio De Janeiro, RJ, Brazil