Hydrated Calcium Silicate Supported CaMoO4 as an Efficient and Recyclable Catalyst for Selective Oxidation of Para-Alkylphenols with Hydrogen Peroxide
MoO 4 2− -H 2 O 2 is an efficient oxidation system for the conversion of para -alkyl-phenols to high value-added para -peroxyquinols and para -quinols, but its large-scale application is still limited to difficulty in catalyst recovery. This paper discloses that a hydrated calcium silicate (CS)-supp...
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Veröffentlicht in: | Catalysis letters 2024-02, Vol.154 (2), p.553-568 |
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Sprache: | eng |
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Zusammenfassung: | MoO
4
2−
-H
2
O
2
is an efficient oxidation system for the conversion of
para
-alkyl-phenols to high value-added
para
-peroxyquinols and
para
-quinols, but its large-scale application is still limited to difficulty in catalyst recovery. This paper discloses that a hydrated calcium silicate (CS)-supported calcium molybdate (CM) catalyst (CMS) is easily fabricated in high-yield and large-scale by simple coprecipitation. Compared to the unsupported CM and Na
2
MoO
4
, CMS has an enhanced catalytic activity for the selective oxidation of
para
-alkyl-phenols, but also it shows a drastically improved selectivity for the target products, which can achieve 84% conversion and 100% selectivity for the goal products in catalyzing the oxidation of 2,4-xylenol with H
2
O
2
in water. Also, it is very efficient for the selective oxidation of other
p
-alkyl substituted phenols in water or methanol, especially including the highly selective oxidation of
p
-cresol which is easy to be overoxidized. More importantly, the CMS catalytic system can be conveniently recovered and repeatedly run without significant activity loss, showing a good reusability. In situ UV-DRS and FT-IR spectra, as well as H
2
O
2
decomposition experiments support that the alkaline CS carrier can induce the reaction of CMS with H
2
O
2
to preferentially generate the mono-/di-peroxomolybdates as the key species for the selective oxidation of
para
-alkyl-phenols.
Graphical Abstract |
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ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-023-04334-x |