Pulse Response Operando Spectroscopy for Resolving Transient Dynamics in the CrOx/Al2O3 Propane Dehydrogenation Catalyst

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Jason P. Malizia*, Stephen Kristy, Rong Xing, James Pittman, Shane Palmer, Shengguang Wang, Mingyong Sun and Rebecca Fushimi*, 
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Abstract

This work introduces an operando spectroscopy reactor based on the Temporal Analysis of Products (TAP) pulse response methodology. This “spectroTAP” reactor enables studies of complex catalyst processes by decoupling gas transport from kinetics under isothermal conditions, greatly simplifying the interpretation of both gas-phase and catalyst surface measurements. The spectroTAP is applied to a CrOx/Al2O3 catalyst used in the dynamic CATOFIN process for propane dehydrogenation (PDH). Four distinct regimes during PDH are resolved by tracking the Cr oxidation state with UV–vis diffuse reflectance spectroscopy in tandem with gas-phase products and reactants. We find that oxygen not associated with the Cr oxidation state must be removed before propane can reduce Cr6+ present in the CrOx lattice to Cr3+. After reduction, there is a transient period of rapid coking concomitant with the main PDH activity. This coking process diminishes much faster than the PDH activity, indicating that carbon deposited during this period does not block PDH active sites. Subsequent oxidative regeneration of the coked catalyst in spectroTAP resolves catalyst oxidation proceeding the carbon combustion. Regenerating the catalyst with large O2 pulses into an inert flow reveals Cr6+ oxides, not gaseous O2, as the species that directly react with surface carbon. These learnings gained from spectroTAP experiments provide a unique vantage point for the future design and operation of next-generation catalysts.

Abstract Image

脉冲响应操作光谱用于解析CrOx/Al2O3丙烷脱氢催化剂的瞬态动力学
本文介绍了一种基于产物时间分析(TAP)脉冲响应方法的operando光谱反应器。这种“spectroTAP”反应器通过在等温条件下将气体输运与动力学解耦,可以研究复杂的催化剂过程,大大简化了气相和催化剂表面测量的解释。该光谱仪应用于丙烷脱氢(PDH)动态CATOFIN工艺中使用的CrOx/Al2O3催化剂。通过紫外-可见漫反射光谱与气相产物和反应物串联跟踪Cr氧化态,解决了PDH过程中的四种不同制度。我们发现,在丙烷将CrOx晶格中的Cr6+还原为Cr3+之前,必须除去与Cr氧化态无关的氧。还原后,有一个短暂的快速焦化伴随着主要的PDH活性。这个焦化过程比PDH活性降低得快得多,这表明在此期间沉积的碳不会阻断PDH活性位点。随后在spectroTAP中焦化催化剂的氧化再生解决了碳燃烧过程中的催化剂氧化。用大的O2脉冲将催化剂再生成惰性流体,结果显示,与表面碳直接反应的是Cr6+氧化物,而不是气态O2。从spectroTAP实验中获得的这些知识为未来下一代催化剂的设计和操作提供了独特的优势。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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