Interfacial synergism of hollow mesoporous Pt/WO/SiO-TiO catalysts enable highly selective hydrogenolysis of glycerol to 1,3-propanediol
Nano Research, ISSN: 1998-0000, Vol: 16, Issue: 7, Page: 9081-9090
2023
- 5Citations
- 10Captures
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Metrics Details
- Citations5
- Citation Indexes5
- CrossRef2
- Captures10
- Readers10
- 10
Article Description
The selective hydrogenolysis of glycerol exhibits great prospects, while the catalysts with high selectivity and activity are still missing and need to be created urgently. Herein, we report the synthesis of hollow mesoporous Pt/WOSiO-TiO nanosphere catalysts with bi-functional interfaces synergistically for high efficiency conversion of glycerol to 1,3-propanediol. The hollow mesoporous Pt/WOSiO-TiO catalysts show a typical brick-concrete liked framework with a high surface area (179.3 mg), large mesopore size (10.6 nm), uniform particle size (~ 400 nm), and ultrathin shell thickness (~ 75 nm). The brick anatase nanocrystals and concrete amorphous SiO networks can selectively rivet Pt nanoparticles and WO nanocluster species, respectively, thus constructing two interfaces for effective adsorption, rapidly catalytic dehydration and hydrogenation processes. The hollow mesoporous Pt/WOSiO-TiO catalysts deliver a high selectivity of 53.8% for 1,3-propanediol (1,3-PDO) at a very high glycerol conversion of 85.0%. As a result, a favorable 1,3-PDO yield of 45.7% can be obtained with excellent stability, which is among the best performances of previously reported catalysts. This work paves a new way to synthesize catalysts with high selectivity, high activity and high stability.[Figure not available: see fulltext.].
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85160284570&origin=inward; http://dx.doi.org/10.1007/s12274-023-5712-0; https://link.springer.com/10.1007/s12274-023-5712-0; https://dx.doi.org/10.1007/s12274-023-5712-0; https://link.springer.com/article/10.1007/s12274-023-5712-0; http://sciencechina.cn/gw.jsp?action=cited_outline.jsp&type=1&id=7614624&internal_id=7614624&from=elsevier
Tsinghua University Press
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