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合成气转化过程中促进作用对锚定胶体氧化铁纳米颗粒生长的影响。

Influence of Promotion on the Growth of Anchored Colloidal Iron Oxide Nanoparticles during Synthesis Gas Conversion.

作者信息

Krans N A, Weber J L, van den Bosch W, Zečević J, de Jongh P E, de Jong K P

机构信息

Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

出版信息

ACS Catal. 2020 Feb 7;10(3):1913-1922. doi: 10.1021/acscatal.9b04380. Epub 2020 Jan 8.

DOI:10.1021/acscatal.9b04380
PMID:32064142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7011703/
Abstract

Using colloidal iron oxide nanoparticles with organic ligands, anchored in a separate step from the supports, has been shown to be beneficial to obtain homogeneously distributed metal particles with a narrow size distribution. Literature indicates that promoting these particles with sodium and sulfur creates an active Fischer-Tropsch catalyst to produce olefins, while further adding an H-ZSM-5 zeolite is an effective way to obtain aromatics. This research focused on the promotion of iron oxide colloids with sodium and sulfur using an inorganic ligand exchange followed by the attachment to H-ZSM-5 zeolite crystals. The catalyst referred to as FeP/Z, which consists of iron particles with inorganic ligands attached to a H-ZSM-5 catalyst, was compared to an unpromoted Fe/Z catalyst and an Fe/Z-P catalyst, containing the colloidal nanoparticles with organic ligands, promoted after attachment. A low CO conversion was observed on both FeP/Z and Fe/Z-P, originating from an overpromotion effect for both catalysts. However, when both promoted catalysts were washed (FeP/Z-W and Fe/Z-P-W) to remove the excess of promoters, the activity was much higher. Fe/Z-P-W simultaneously achieved low selectivity toward methane as part of the promoters were still present after washing, whereas for FeP/Z-W the majority of promoters was removed upon washing, which increased the methane selectivity. Moreover, due to the addition of Na+S promoters, the iron nanoparticles in the FeP/Z(-W) catalysts had grown considerably during catalysis, while those in Fe/Z-P(-W) and Fe/Z(-W) remained relatively stable. Lastly, as a large broadening of particle sizes for the used FeP/Z-W was found, where particle sizes had both increased and decreased, Ostwald ripening is suggested for particle growth accelerated by the presence of the promoters.

摘要

使用带有有机配体的胶体氧化铁纳米颗粒,在与载体分开的步骤中进行锚定,已被证明有利于获得尺寸分布窄且均匀分布的金属颗粒。文献表明,用钠和硫对这些颗粒进行促进可生成活性费托催化剂以生产烯烃,而进一步添加H-ZSM-5沸石是获得芳烃的有效方法。本研究重点在于通过无机配体交换用钠和硫促进氧化铁胶体,随后将其附着到H-ZSM-5沸石晶体上。将称为FeP/Z的催化剂(由附着有无机配体的铁颗粒与H-ZSM-5催化剂组成)与未促进的Fe/Z催化剂以及Fe/Z-P催化剂进行比较,Fe/Z-P催化剂含有带有有机配体的胶体纳米颗粒,在附着后进行促进。在FeP/Z和Fe/Z-P上均观察到低的CO转化率,这源于两种催化剂的过度促进效应。然而,当对两种促进的催化剂进行洗涤(FeP/Z-W和Fe/Z-P-W)以去除过量的促进剂时,活性要高得多。Fe/Z-P-W同时实现了对甲烷的低选择性,因为洗涤后仍有部分促进剂存在,而对于FeP/Z-W,大部分促进剂在洗涤时被去除,这增加了甲烷选择性。此外,由于添加了Na+S促进剂,FeP/Z(-W)催化剂中的铁纳米颗粒在催化过程中显著生长,而Fe/Z-P(-W)和Fe/Z(-W)中的铁纳米颗粒保持相对稳定。最后,由于发现使用过的FeP/Z-W的粒径大幅变宽,粒径既有增大也有减小,因此认为奥斯特瓦尔德熟化是由促进剂的存在加速的颗粒生长过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/f062946079be/cs9b04380_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/b0d17ad9de07/cs9b04380_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/0bbd1ea83c71/cs9b04380_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/8c40244f7576/cs9b04380_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/ee87249bf5a8/cs9b04380_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/f062946079be/cs9b04380_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/b0d17ad9de07/cs9b04380_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/0bbd1ea83c71/cs9b04380_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/8c40244f7576/cs9b04380_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/ee87249bf5a8/cs9b04380_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2d/7011703/f062946079be/cs9b04380_0005.jpg

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