果胶驱动溶胶-凝胶法合成甲苯催化氧化MnOx的研究

Q3 Materials Science JCIS open Pub Date : 2023-04-01 DOI:10.1016/j.jciso.2023.100076
Jinggang Zhao , Peifen Wang , Jing Wang , Xiaoxun Ma , Lei Shi , Guangwen Xu , Abuliti Abudula , Guoqing Guan
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引用次数: 1

摘要

将一种新型的绿色果胶驱动的自燃烧溶胶凝胶成功应用于氧化锰催化剂的合成,与传统柠檬酸和甘氨酸驱动的溶胶凝胶合成氧化锰催化剂相比,该催化剂对甲苯的低温燃烧表现出优异的催化性能。表征结果表明,本方法合成的MnOx-P催化剂具有独特的分级介孔结构,结晶度较低,晶粒尺寸较小,活性物种丰富,结构缺陷。与传统溶胶-凝胶法合成的催化剂相比,MnOx-P催化剂具有优异的低温还原性能和更好的氧迁移率,这被认为是螯合和煅烧过程特定相互作用的结果。此外,MnOx-P催化剂在甲苯催化燃烧过程中表现出令人满意的长期稳定性和耐水性。
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Synthesis of MnOx from pectin-driven sol-gel route for catalytic oxidation of toluene

A novel green pectin-driven sol-gel with an auto-combustion route was successfully applied for the synthesis of manganese oxide catalysts, which exhibited superior catalytic performance for low-temperature combustion of toluene compared to those cases using manganese oxide catalysts synthesized by traditional citric acid and glycine-driven sol-gel routes. The characterization results showed that the MnOx-P catalyst synthesized by the present method exhibited a unique hierarchical mesoporous structure with lower crystallinity and smaller grain size, leading to abundant active species and defect structures. Comparing with the catalysts synthesized by those traditional sol-gel methods, the MnOx-P catalyst had excellent low-temperature reducible performance and better oxygen mobility, which is considered to be resulted from the specific interaction of chelation and calcination processes. In addition, the MnOx-P catalyst exhibited satisfactory long-term stability and water tolerance during catalytic toluene combustion process.

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来源期刊
JCIS open
JCIS open Physical and Theoretical Chemistry, Colloid and Surface Chemistry, Surfaces, Coatings and Films
CiteScore
4.10
自引率
0.00%
发文量
0
审稿时长
36 days
期刊最新文献
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