Effect of Ag addition on performance of Au/TS-1-B catalyst in gas phase propylene epoxidation

YANG Jia; ZHANG Zhihua; FENG Xiang; DUAN Xuezhi; ZHOU Jinghong; ZHOU Xinggui

doi:10.11949/j.issn.0438-1157.20160281

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Effect of Ag addition on performance of Au/TS-1-B catalyst in gas phase propylene epoxidation

更新时间：2025-12-10

- Effect of Ag addition on performance of Au/TS-1-B catalyst in gas phase propylene epoxidation
- CIESC Journal Issue 9, Pages: 3684-3691(2016)
- 作者机构：
  
  华东理工大学化学工程联合国家重点实验室,上海,200237
- 作者简介：
- 基金信息：
- DOI：10.11949/j.issn.0438-1157.20160281
  CLC： 643.32
- Online First：05 September 2016，
  
  Published：05 September 2016
- 稿件说明：
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YANG Jia, ZHANG Zhihua, FENG Xiang, et al. Effect of Ag addition on performance of Au/TS-1-B catalyst in gas phase propylene epoxidation[J]. CIESC Journal, 2016, (9): 3684-3691.
DOI：

YANG Jia, ZHANG Zhihua, FENG Xiang, et al. Effect of Ag addition on performance of Au/TS-1-B catalyst in gas phase propylene epoxidation[J]. CIESC Journal, 2016, (9): 3684-3691. DOI： 10.11949/j.issn.0438-1157.20160281.

摘要

以堵孔钛硅分子筛（TS-1-B）为载体，通过沉积-沉淀法制备了金催化剂（Au/TS-1-B）和金-银双金属催化剂（Au-Ag/TS-1-B），考察两个催化剂在丙烯气相环氧化反应中的稳定性，并利用HRTEM、Py-GC-MS和UV-vis DRS等手段对金属颗粒粒径变化、结焦量及结焦种类等进行了表征。结果表明，Ag的引入显著降低了催化剂表面焦类物质总量和结焦中低聚烯烃的相对含量，从而显著提升了催化剂的稳定性。

Abstract

Propylene epoxide (PO)

as a versatile bulk chemical intermediate

is widely used in the production of a variety of derivatives. Direct propene epoxidation with molecular H2 and O2 to synthesize PO is a greener

simpler and more sustainable route compared with traditional chlorohydrin and several organic hydroperoxide processes. In this study the uncalcined titanium silicate-1 with blocked micropores (TS-1-B) was used to support Au nanoparticles (Au/TS-1-B) for direct propylene epoxidation with hydrogen and oxygen. Au-Ag/TS-1-B was prepared by sequential deposition-precipitation method followed by in-situ reduction to improve the performance of the catalyst. After introducing Ag

the catalytic stability was improved. UV-vis DRS analysis showed the existence of Ag-Au bimetallic particles. It was observed from HRTEM results that the metal particle size was much smaller on Au-Ag/TS-1-B than on Au/TS-1-B and the particle size of the metal particles on both catalysts did not change during the reaction process. Moreover

pyrolysis GC-MS results showed less coke was formed on Au-Ag/TS-1-B and coke could be reduced by regeneration. All these accounted for the significantly improved activity and stability of Au-Ag/TS-1-B catalyst.

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