Restructuring of Ag catalysts for methanol to formaldehyde conversion studied using in situ X-ray ptychography and electron microscopy

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Srashtasrita Das, Maik Kahnt, Youri van Valen, Tina Bergh, Sara Blomberg, Mikhail Lyubomirskiy, Christian G. Schroer, Hilde J. Venvik, Thomas L. Sheppard
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Abstract

Dynamic restructuring of silver catalysts during the industrial conversion of methanol to formaldehyde leads to surface faceting and pinhole formation. Subsequent sintering under reaction conditions, followed by increased pressure drop and decreased catalyst activity requires catalyst bed replacement after several months of operation. This necessitates a comprehensive understanding of the bulk catalyst restructuring under exposure to different gas environments. In this work, Ag restructuring was studied at elevated temperatures under different reactive and inert gas environments. Bubble formation within catalysts of 5–8 μm thickness was visualized in real-time using in situ X-ray ptychography. Stepwise heating up to 650 °C in combination with imaging was used to determine the effect of temperature on silver restructuring. Dynamic changes within the catalyst were further quantified in terms of relative changes in mass on selected regions at a constant temperature of 500 °C. Quantitative assessment of dynamic changes in the catalyst resulting from bubble growth and movement revealed the influence of temperature, time, and gas environment on the degree of restructuring. Post-mortem scanning electron microscopy with energy-dispersive X-ray spectroscopy mapping confirmed the redistribution of material as a consequence of bubble rupture and collapse. The formation of pores and cavities under different gas environments was additionally confirmed using a fixed bed reactor, and subsequent examination using focused-ion beam milling, providing detailed analysis of the surface structure. This study demonstrates the unique advantage of correlative hard X-ray and electron microscopy for quantitative morphological studies of industrial catalysts.

Abstract Image

利用原位 X 射线层析成像和电子显微镜研究甲醇到甲醛转化过程中银催化剂的结构重组
在甲醇到甲醛的工业转化过程中,银催化剂的动态重组会导致表面刻面和针孔的形成。随后,催化剂在反应条件下发生烧结,压降增大,催化剂活性降低,因此需要在运行数月后更换催化剂床层。这就需要全面了解催化剂在不同气体环境下的结构重组。在这项工作中,研究了在不同反应性气体和惰性气体环境下高温条件下的 Ag 重组。利用原位 X 射线层析技术实时观察了厚度为 5-8 μm 的催化剂内部气泡的形成。将催化剂逐步加热至 650 °C,同时进行成像,以确定温度对银重组的影响。在 500 ℃ 恒温条件下,根据选定区域质量的相对变化,进一步量化了催化剂内部的动态变化。对气泡生长和移动导致的催化剂动态变化的定量评估显示了温度、时间和气体环境对重组程度的影响。死后扫描电子显微镜和能量色散 X 射线光谱图证实了气泡破裂和坍塌导致的材料重新分布。此外,还使用固定床反应器确认了不同气体环境下孔隙和空腔的形成,随后使用聚焦离子束铣进行了检查,提供了表面结构的详细分析。这项研究证明了硬 X 射线和电子显微镜在对工业催化剂进行定量形态研究方面的独特优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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