Dual anchoring strategy to construct low metal loading Co/BEA catalysts for propane dehydrogenation†

IF 4.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Yulai Lin , Jun Liang , Zijun Huang , Jiaming Dong , Yongming Luo , Dedong He
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引用次数: 0

Abstract

Cobalt-based catalysts have garnered significant attention in propane dehydrogenation (PDH) due to their cost-effectiveness and environmental compatibility, where the properties of Co species dictate catalytic performance. However, conventional synthesis methods fail to simultaneously achieve precise encapsulation and structural stabilization of Co sites under harsh PDH conditions. Herein, we propose an innovative dual-anchoring strategy that synergizes strong electrostatic adsorption (SEA) and secondary crystallization (SC) to engineer highly stable yet active Co centers at low metal loadings (actually 0.125 wt%). The SEA process enables directional anchoring of Co precursors within silanol nests of dealuminated BEA zeolite, while the SC treatment prevents Co aggregation. This synergistic approach yields tetrahedral Co2+ (Td-Co2+) sites with exceptional dispersion and optimized Lewis acidity, which achieved ultra-long PDH stability of up to 110 hours and specific activity surpassing most reported catalysts.

Abstract Image

构建低金属负荷Co/BEA丙烷脱氢催化剂的双锚定策略
钴基催化剂由于其成本效益和环境相容性在丙烷脱氢(PDH)中引起了极大的关注,其中Co物种的性质决定了催化性能。然而,在恶劣的PDH条件下,传统的合成方法无法同时实现Co位点的精确包封和结构稳定。在此,我们提出了一种创新的双锚定策略,该策略协同强静电吸附(SEA)和二次结晶(SC),以在低金属负载(实际为0.125 wt%)下设计高度稳定且活性的Co中心。SEA工艺可以将Co前体定向锚定在脱铝BEA沸石的硅醇巢内,而SC处理可以防止Co聚集。这种协同方法产生了四面体Co2+ (Td-Co2+)位点,具有优异的分散性和优化的Lewis酸度,实现了长达110小时的PDH稳定性,比活性超过了大多数报道的催化剂。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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