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机械活化辅助碳热还原法合成碳化钒

Synthesis of Vanadium Carbide by Mechanical Activation Assisted Carbothermic Reduction.

作者信息

Zaki Zaki I, El-Sadek Mohamed H, Ali Heba H, Ahmed Hesham

机构信息

Department of Chemistry, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.

Pyrometallurgy Department, Minerals Technology Division, Central Metallurgical R&D Institute (CMRDI), P.O Box 87, Cairo 11865, Egypt.

出版信息

Materials (Basel). 2020 Oct 2;13(19):4408. doi: 10.3390/ma13194408.

Abstract

Vanadium carbide is known, for its hardness and other unique properties, as a refractory material. The synthesis of vanadium carbide is always associated with the utilization of expensive active metals, such as aluminum, calcium and magnesium, as a reducing agent to extract the vanadium metal from its corresponding oxide, followed by carbidization. The carbidization of reduced vanadium requires a complicated process and elevated temperature. Mechanical activation to synthesize vanadium carbide from its corresponding oxide and carbon source represents a promising, straightforward and less energy-intensive route. In the present study, vanadium carbide is synthesized by the carbothermic reduction of a mechanically activated mixture of VO and carbon black as reducing agents without any additives. The reduction process is monitored by means of thermogravimetric analysis. The reduction products are characterized by X-ray diffraction and field emission scanning electron microscope. It is found that VC with an average crystallite size of 88 nm can be synthesized from a VO-C mixture after milling for 15 h and further heating at 1050 °C for 1 h in an inert atmosphere.

摘要

碳化钒因其硬度和其他独特性能而被视为一种耐火材料。碳化钒的合成总是与使用昂贵的活性金属(如铝、钙和镁)作为还原剂相关联,以便从相应的氧化物中提取钒金属,随后进行碳化。还原钒的碳化过程需要复杂的工艺和高温。通过机械活化由相应的氧化物和碳源合成碳化钒是一条有前景、直接且能耗较低的途径。在本研究中,通过碳热还原机械活化的VO和炭黑混合物作为还原剂来合成碳化钒,且不添加任何添加剂。通过热重分析监测还原过程。用X射线衍射和场发射扫描电子显微镜对还原产物进行表征。结果发现,在惰性气氛中研磨15小时并在1050℃进一步加热1小时后,可从VO - C混合物中合成平均微晶尺寸为88nm的VC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09b5/7579465/0793c81bf368/materials-13-04408-g001.jpg

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