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1,1-二甲基肼在Pt/SiO催化剂上转化的机理研究。

Mechanistic study of 1,1-dimethylhydrazine transformation over Pt/SiO catalyst.

作者信息

Smirnov Andrei V, Kots Pavel A, Panteleyev Maksim A, Ivanova Irina I

机构信息

Department of Chemistry, Lomonosov Moscow State University Leninskiye Gory 1, bld. 3 11991 Moscow Russia.

A.V. Topchiev Institute of Petrochemical Synthesis Leninskiye prospect 29 11991 Moscow Russia.

出版信息

RSC Adv. 2018 Nov 1;8(64):36970-36979. doi: 10.1039/c8ra07769j. eCollection 2018 Oct 26.

DOI:10.1039/c8ra07769j
PMID:35558958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9089307/
Abstract

Catalytic oxidation of 1,1-dimethylhydrazine (UDMH) with molecular oxygen over Pt/SiO was studied by FTIR spectroscopy coupled with online MS monitoring of the gas phase. An unusual two-step oxidation process was detected in experiments with the pulse UDMH feeding: initial UDMH oxidation over a fresh platinum surface quickly terminates due to the blockage of active sites; a time-separated second oxidation step corresponds to combustion of the surface residue. This residue consists of C[triple bond, length as m-dash]N nitrile groups formed decomposition of the products of non-oxidative UDMH conversion, such as dimethylamine. The two-step oxidation picture is observed over a broad range of reaction temperatures and oxygen to UDMH ratios.

摘要

通过傅里叶变换红外光谱(FTIR)结合气相在线质谱监测,研究了在Pt/SiO上用分子氧催化氧化偏二甲肼(UDMH)的过程。在脉冲进料UDMH的实验中检测到一个不寻常的两步氧化过程:在新鲜铂表面上最初的UDMH氧化由于活性位点的堵塞而迅速终止;时间上分开的第二步氧化对应于表面残留物的燃烧。该残留物由非氧化UDMH转化产物(如二甲胺)分解形成的C≡N腈基组成。在很宽的反应温度和氧与UDMH比例范围内都观察到了两步氧化情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/750a/9089307/fb79a996fa39/c8ra07769j-f7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/750a/9089307/8e227ea19e16/c8ra07769j-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/750a/9089307/fb79a996fa39/c8ra07769j-f7.jpg

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