One-pot preparation of mesoporous KPMoO ( = 1, 2, 3, 4) materials for oxidative desulfurization: electrochemically-active surface area (ECSA) determines their activity

A series of pure polyoxometalate salts, K x [PMo 12 O 40 ] 3− (K x PMo, x = 1, 2, 3, 4), have been successfully prepared via a one pot hydrothermal method using F127 as a template. These obtained K x PMo materials are mesoporous, and have high surface area (>40 m 2 g −1 ) without depending on the...

Full description

Saved in:
Bibliographic Details
Published inReaction chemistry & engineering Vol. 5; no. 9; pp. 1776 - 1782
Main Authors He, Jun, Guan, Lifang, Zhou, Yiqian, Shao, Peipei, Yao, Yue, Lu, Shuxiang, Kong, Lingbo, Liao, Xiaoyuan
Format Journal Article
LanguageEnglish
Published 25.08.2020
Online AccessGet full text

Cover

Loading…
More Information
Summary:A series of pure polyoxometalate salts, K x [PMo 12 O 40 ] 3− (K x PMo, x = 1, 2, 3, 4), have been successfully prepared via a one pot hydrothermal method using F127 as a template. These obtained K x PMo materials are mesoporous, and have high surface area (>40 m 2 g −1 ) without depending on the supports. In particular, these K x PMo materials display an increased efficiency towards oxidative desulfurization (ODS). These materials could be reused, and result in the complete desulfurization of diesel in 1 h. In addition, our experimental test shows that the high activity of K x PMo catalysts (such as K 1.0 PMo, K 2.0 PMo, K 3.0 PMo and K 4.0 PMo) are linearly correlated with their electrochemically-active surface area (ECSA). K 4.0 PMo has the largest ECSA value and exposes largest number anions ([PMo 12 O 40 ] 3− ), resulting in the best ODS activity. This study reveals the role of ECSA in the ODS reaction, providing a new understanding for ODS in mesoporous K x PMo materials. A series of pure polyoxometalate salts, K x [PMo 12 O 40 ] 3− (K x PMo, x = 1, 2, 3, 4), have been successfully prepared via a one pot hydrothermal method using F127 as a template.
Bibliography:10.1039/d0re00213e
Electronic supplementary information (ESI) available. See DOI
ISSN:2058-9883
DOI:10.1039/d0re00213e