Low-Waste Synthesis and Properties of Highly Dispersed NiO·Al2O3 Mixed Oxides Based on the Products of Centrifugal Thermal Activation of Gibbsite

IF 2.8 Q2 ENGINEERING, CHEMICAL
A. Zhuzhgov, L. Isupova, E. A. Suprun, A. Gorkusha
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Abstract

This study revealed an increased reactivity of centrifugally thermoactivated products of gibbsite toward aqueous solutions of nickel nitrate at room temperature as well as under hydrothermal conditions. X-ray, thermal, microscopy, adsorption and chemical analysis methods were used to investigate and demonstrate the possibility of obtaining highly loaded mixed aluminum–nickel oxide systems, with a nickel content of ca. 33 wt.%, using a hydrochemical treatment at room temperature or a hydrothermal treatment of suspensions of the product of the centrifugal thermal activation of gibbsite in aqueous solutions of nickel nitrate. It was shown that the thermal treatment of xerogels—hydrochemical interaction products—in the range of 350–850 °C led to the formation of NiO phases and highly dispersed solid solutions of nickel based on the NiAl2O4 spinel structure, with different ratios and a high specific surface area of 140–200 m2/g. A hydrochemical treatment of suspensions at room temperature ensures that the predominant formation of the NiO phase is distributed over the surface of the alumina matrix after calcination, whereas hydrothermal treatment at 150 °C leads to a deeper interaction of the suspension components at the treatment step, which occurs after the thermal treatment of the formed xerogel in the predominant formation of poorly crystallized NiAl2O4 spinel (“protospinel”). The considered method makes it possible to obtain complex aluminum–nickel oxide systems with different phase ratios, decreases the number of initial reagents and synthesis steps, completely excludes waste and diminishes the total amount of nitrates by 75 wt.% compared to the classical nitrate scheme for the coprecipitation of compounds with a similar elemental composition.
基于赤铁矿离心热活化产物的高分散NiO·Al2O3混合氧化物的低废料合成及性能
本研究表明,在室温和水热条件下,三水铝石离心热活化产物对硝酸镍水溶液的反应性增强。x射线、热、显微镜、吸附和化学分析方法被用来研究和证明获得高负载的混合铝镍氧化物体系的可能性,镍含量约为33 wt.%,在室温下使用水化学处理或水热处理的悬浮液的产品的离心热活化在硝酸镍水溶液中。结果表明,在350 ~ 850℃范围内对干凝胶(水化学相互作用产物)进行热处理,形成了以NiAl2O4尖晶石结构为基础的NiO相和高度分散的镍固溶体,其比例不同,比表面积高达140 ~ 200 m2/g。在室温下对悬浮液进行水化学处理,确保焙烧后NiO相的主要形成分布在氧化铝基体表面,而在150°C下的水热处理导致悬浮液组分在处理步骤中发生更深的相互作用,这发生在形成的干燥凝胶在主要形成的不良结晶的NiAl2O4尖晶石(“原尖晶石”)的热处理之后。所考虑的方法使得获得具有不同相比的复杂铝镍氧化物体系成为可能,减少了初始试剂的数量和合成步骤,完全排除了浪费,并且与具有相似元素组成的化合物的经典硝酸盐共沉淀方案相比,减少了75%的硝酸盐总量。
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
ChemEngineering
ChemEngineering Engineering-Engineering (all)
CiteScore
4.00
自引率
4.00%
发文量
88
审稿时长
11 weeks
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