|
Type
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Journal
Article
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|
Author
|
Jennifer
K. Edwards
|
|
Author
|
Simon
J. Freakley
|
|
URL
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|
|
Series
|
Perspectives
in the H2O2 direct synthesis reaction process
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|
Volume
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248
|
|
Pages
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3-9
|
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Publication
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Catalysis
Today
|
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Date
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June
15, 2015
|
|
Abstract
|
The
direct synthesis of hydrogen peroxide has attracted considerable research
interest into catalysts which could provide an alternative to the current
industrial process. Many catalyst systems have been evaluated, most of which
utilize Pd as the active component. The activity of the catalysts can be
promoted in a number of ways, either by addition of a second metal, or by
adding promoters into the reactant phase such as acid and halides. Acidic
supports can increase the activity of catalysts without addition of aqueous
acids by minimizing the decomposition of hydrogen peroxide, and catalysts can
be doped with halide ions to minimize the non-selective hydrogenation reaction.
The addition of gold to form bimetallic particles has also been shown to
increase hydrogen peroxide yield by increasing hydrogen selectivity without
the need to add acid and halides.
Recent research on the direct synthesis of hydrogen peroxide has focused on the use of continuous reactor systems such as membrane, fixed bed and microreactors. Recent literature regarding catalyst design and continuous process development as well as historical perspective of the process is discussed in this review. |
Thursday, August 6, 2015
Advances in the direct synthesis of hydrogen peroxide from hydrogen and oxygen
Advances
in the direct synthesis of hydrogen peroxide from hydrogen and oxygen
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