In Situ Study of the High-Temperature Solid-Phase Synthesis of Zinc Tungstate in the Zinc Oxide–Tungsten Oxide System

A. V. Mostovshchikov, D. S. Tokarev, F. A. Gubarev, A. V. Pirozhkov, D. V. Tikhonov
{"title":"In Situ Study of the High-Temperature Solid-Phase Synthesis of Zinc Tungstate in the Zinc Oxide–Tungsten Oxide System","authors":"A. V. Mostovshchikov,&nbsp;D. S. Tokarev,&nbsp;F. A. Gubarev,&nbsp;A. V. Pirozhkov,&nbsp;D. V. Tikhonov","doi":"10.1134/S1027451024701428","DOIUrl":null,"url":null,"abstract":"<p>Zinc tungstate is an inorganic luminescent material with the self-activation of luminescence when exposed to ultraviolet (UV) radiation, X-rays, and cathode rays. There are two ways to synthesize this compound: the liquid-phase sol-gel method and solid-phase high-temperature synthesis in an oxygen-containing environment. Phase transformations are studied during the solid-phase high-temperature synthesis of ZnWO<sub>4</sub> from a mixture of micron-sized powders of ZnO and WO<sub>3</sub> oxides upon heating to 900°C and storage for 30 min in air. It is experimentally established that during high-temperature solid-phase synthesis, in the entire studied temperature range, zinc oxide does not change its crystalline structure upon heating, while tungsten oxide undergoes a series of transformations from the monoclinic phase to the orthorhombic phase. The formation of the crystalline hexagonal phase of zinc tungstate begins in the temperature range from 700 to 750°C. At a maximum temperature of 900°C, the phases ZnWO<sub>4</sub> (monoclinic), ZnO (hexagonal), and WO<sub>3</sub> (orthorhombic) coexist simultaneously; further storage at this temperature leads to an increase in the content of the zinc-tungstate phase and a decrease in the concentration of other phases.</p>","PeriodicalId":671,"journal":{"name":"Journal of Surface Investigation: X-ray, Synchrotron and Neutron Techniques","volume":"18 6","pages":"1477 - 1481"},"PeriodicalIF":0.4000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Surface Investigation: X-ray, Synchrotron and Neutron Techniques","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1134/S1027451024701428","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHYSICS, CONDENSED MATTER","Score":null,"Total":0}
引用次数: 0

Abstract

Zinc tungstate is an inorganic luminescent material with the self-activation of luminescence when exposed to ultraviolet (UV) radiation, X-rays, and cathode rays. There are two ways to synthesize this compound: the liquid-phase sol-gel method and solid-phase high-temperature synthesis in an oxygen-containing environment. Phase transformations are studied during the solid-phase high-temperature synthesis of ZnWO4 from a mixture of micron-sized powders of ZnO and WO3 oxides upon heating to 900°C and storage for 30 min in air. It is experimentally established that during high-temperature solid-phase synthesis, in the entire studied temperature range, zinc oxide does not change its crystalline structure upon heating, while tungsten oxide undergoes a series of transformations from the monoclinic phase to the orthorhombic phase. The formation of the crystalline hexagonal phase of zinc tungstate begins in the temperature range from 700 to 750°C. At a maximum temperature of 900°C, the phases ZnWO4 (monoclinic), ZnO (hexagonal), and WO3 (orthorhombic) coexist simultaneously; further storage at this temperature leads to an increase in the content of the zinc-tungstate phase and a decrease in the concentration of other phases.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
氧化锌-氧化钨体系高温固相合成钨酸锌的原位研究
钨酸锌是一种无机发光材料,在紫外线、x射线和阴极射线照射下具有自激活发光特性。该化合物有两种合成方法:液相溶胶-凝胶法和固相含氧高温合成法。将微米级氧化锌和WO3氧化物混合粉末加热到900℃,在空气中储存30 min,研究了固相高温合成ZnWO4的相变。实验证实,在高温固相合成过程中,在整个研究温度范围内,氧化锌在加热后不改变其晶体结构,而氧化钨则经历了从单斜相到正交相的一系列转变。钨酸锌六方晶相的形成始于700 ~ 750℃。在最高温度900℃时,ZnWO4(单斜晶)、ZnO(六方晶)和WO3(正交晶)相同时存在;在此温度下进一步贮存会导致钨酸锌相含量的增加和其他相浓度的降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
0.90
自引率
25.00%
发文量
144
审稿时长
3-8 weeks
期刊介绍: Journal of Surface Investigation: X-ray, Synchrotron and Neutron Techniques publishes original articles on the topical problems of solid-state physics, materials science, experimental techniques, condensed media, nanostructures, surfaces of thin films, and phase boundaries: geometric and energetical structures of surfaces, the methods of computer simulations; physical and chemical properties and their changes upon radiation and other treatments; the methods of studies of films and surface layers of crystals (XRD, XPS, synchrotron radiation, neutron and electron diffraction, electron microscopic, scanning tunneling microscopic, atomic force microscopic studies, and other methods that provide data on the surfaces and thin films). Articles related to the methods and technics of structure studies are the focus of the journal. The journal accepts manuscripts of regular articles and reviews in English or Russian language from authors of all countries. All manuscripts are peer-reviewed.
期刊最新文献
Electrical Discharge Machining of Molybdenum Surface Determination of the Phase Composition of Vanadium Oxide Nanofibers Piezo-Photocatalytic Decomposition of Metronidazole Using ZnO Microtetrapods under Simulated Sunlight Study of the Initiation of Nuclear Reactions in Boron-Containing Targets by a Beam of Deuterium Ions with an Energy of <50 keV at the HELIS Ion Accelerator Surface Modification of Commercially Pure Titanium by Combining Plasma-Electrolytic Carburizing, Polishing, and Microarc Oxidation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1