Article(id=1304141574422688241, tenantId=1146029695717560320, journalId=1303687303576780880, issueId=1304141567850213817, articleNumber=null, orderNo=null, doi=10.3969/j.issn.1009-3842.2026.03.011, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1758988800000, receivedDateStr=2025-09-28, revisedDate=1766073600000, revisedDateStr=2025-12-19, acceptedDate=null, acceptedDateStr=null, onlineDate=1788861181120, onlineDateStr=2026-09-08, pubDate=1782576000000, pubDateStr=2026-06-28, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788861181120, onlineIssueDateStr=2026-09-08, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788861181120, creator=13701087609, updateTime=1788861181120, updator=13701087609, issue=Issue{id=1304141567850213817, tenantId=1146029695717560320, journalId=1303687303576780880, year='2026', volume='', issue='3', pageStart='1', pageEnd='134', issueExtLink='null', onlineDate='null', pubDate='1782576000000', pubDateStr='2026-06-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788861179554, creator='13701087609', updateTime=1788924930580, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304408959088092087, tenantId=1146029695717560320, journalId=1303687303576780880, issueId=1304141567850213817, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304408959088092088, tenantId=1146029695717560320, journalId=1303687303576780880, issueId=1304141567850213817, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=95, endPage=103, ext={EN=ArticleExt(id=1304141574653374962, articleId=1304141574422688241, tenantId=1146029695717560320, journalId=1303687303576780880, language=EN, title=Fundamental Research on Carbothermal Reduction of WO3 to Prepare WO2, columnId=1304141568877814747, journalTitle=Copper Engineering, columnName=Material Preparation and Process Engineering, runingTitle=null, highlight=null, articleAbstract=

WO2 is the important intermediate product during the carbothermal reduction of WO3 to WC, and the systematical analysis of the reduction behavior of WO3 to WO2 has a significant role on the efficient preparation of WC. Reaction behavior of carbothermal reduction of WO3 to WO2 was investigated with adaptation of thermogravimetric (TG), X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and thermodynamic calculation technologies. Influences of different parameters, such as reduction temperature, C/WO3 molar ratio, and reaction time, on the phase transition and morphological evolution during the process were considered. Results of non-isothermal reduction experiment from room temperature to 1200 ℃ showed that WO3 was preferentially reduced into WO2.72, then to WO2, and finally to metallic W. Phase transition law agreed well with thermodynamic theoretical calculation result. In the range of 1000 to 1050 ℃, with the increase of C/WO3 molar ratio, the relative content of WO2.72 in the reaction product gradually decreased, while that of WO2 increased. Single-phase WO2 can be prepared at the C/WO3 molar ratio of 1.1. However, when the C/WO3 molar ratio increased to 1.2, W formed due to the excess C. During the whole carbothermal reduction process, granular WO3 was first in contact with honeycomb activated carbon. As the increase of reaction time, heat transfer process began and then chemical reaction between the two reactants occurred to form columnar WO2.72. Subsequently, the columnar WO2.72 was further reduced into elliptical WO2. Based on experimental results, the optimal conditions for preparing well-dispersed WO2 were determined as follows: reduction temperature of 1050 ℃, C/WO3 molar ratio of 1.1, and reaction time of 90 min.

, authors=Chunhua Yang1, Yulong Zhang2, Lu Wang1, 2, Aiguo Zhu3, authorsList=Chunhua Yang, Yulong Zhang, Lu Wang, Aiguo Zhu, authorCompany=null, correspAuthors=Lu Wang, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1304141575890694643, articleId=1304141574422688241, tenantId=1146029695717560320, journalId=1303687303576780880, language=CN, title=碳热还原WO3制备WO2基础研究, columnId=1304141569037198301, journalTitle=铜业工程, columnName=材料制备与加工工程, runingTitle=null, highlight=null, articleAbstract=

WO2是碳热还原WO3制备WC的重要中间产物,系统研究WO3→WO2的碳热还原行为对高效制备WC至关重要。以Ar为反应气氛,结合热重(TG),X射线衍射(XRD),场发射扫描电子显微镜(FESEM)和热力学计算等方法,对碳热还原WO3制备WO2的反应行为进行了研究,重点考察了还原温度、C/WO3摩尔比和反应时间对制备进程中样品物相转变和形貌演变的影响。结果表明,在室温至1200 ℃的变温实验中,WO3优先还原成WO2.72,之后还原成WO2,最后生成金属W。物相转变规律与热力学理论计算结果相符。在1000~1050 ℃范围内,随着C/WO3摩尔比的增加,反应产物中WO2.72含量逐渐降低,WO2含量逐渐升高,并且在C/WO3摩尔比为1.1时可得单相WO2。在整个碳热还原过程中,颗粒状WO3优先与蜂窝状活性炭充分接触并均匀混合。随着反应时间的增加,两者间开始进行热量传输并发生反应生成柱状WO2.72。之后,柱状WO2.72再进一步被还原成椭圆形WO2。并据此得出了制备分散性良好WO2的最佳条件:还原温度为1050 ℃,C/WO3摩尔比为1.1,反应时间为90 min。

, authors=杨春华1, 张宇龙2, 王璐1, 2, 朱爱国3, authorsList=杨春华, 张宇龙, 王璐, 朱爱国, authorCompany=null, correspAuthors=王璐, authorNote=

杨春华(1988—),男,江苏泰州人,工程师,研究方向:材料成型与调控,E-mail:

, correspAuthorsNote=
王璐,副教授,E-mail:
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杨春华(1988—),男,江苏泰州人,工程师,研究方向:材料成型与调控,E-mail:

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杨春华(1988—),男,江苏泰州人,工程师,研究方向:材料成型与调控,E-mail:

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碳热还原WO3制备WO2基础研究
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杨春华 1 , 张宇龙 2 , 王璐 1, 2 , 朱爱国 3
铜业工程 | 材料制备与加工工程 2026,(3): 95-103
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铜业工程 |材料制备与加工工程 2026 , (3) : 95 -103
碳热还原WO3制备WO2基础研究
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杨春华1 , 张宇龙2, 王璐1, 2 , 朱爱国3
作者信息
  • 1.泰州伍伦肱智能科技有限公司,江苏 泰州 225502
  • 2.武汉科技大学 钢铁冶金及资源利用教育部重点实验室,湖北 武汉 430081
  • 3.江苏省安全生产宣传教育中心,江苏 南京 210042
通讯作者:
王璐,副教授,E-mail:
作者简介:

杨春华(1988—),男,江苏泰州人,工程师,研究方向:材料成型与调控,E-mail:

Fundamental Research on Carbothermal Reduction of WO3 to Prepare WO2
Chunhua Yang1 , Yulong Zhang2, Lu Wang1, 2 , Aiguo Zhu3
Affiliations
  • 1.Taizhou Wulungong Intelligent Technology Co.,Ltd.,Taizhou 225502,China
  • 2.Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education,Wuhan University of Science and Technology,Wuhan 430081,China
  • 3.Publicity and Education Center of Work Safety of Jiangsu Province,Nanjing 210042,China
出版时间: 2026-06-28 doi: 10.3969/j.issn.1009-3842.2026.03.011
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WO2是碳热还原WO3制备WC的重要中间产物,系统研究WO3→WO2的碳热还原行为对高效制备WC至关重要。以Ar为反应气氛,结合热重(TG),X射线衍射(XRD),场发射扫描电子显微镜(FESEM)和热力学计算等方法,对碳热还原WO3制备WO2的反应行为进行了研究,重点考察了还原温度、C/WO3摩尔比和反应时间对制备进程中样品物相转变和形貌演变的影响。结果表明,在室温至1200 ℃的变温实验中,WO3优先还原成WO2.72,之后还原成WO2,最后生成金属W。物相转变规律与热力学理论计算结果相符。在1000~1050 ℃范围内,随着C/WO3摩尔比的增加,反应产物中WO2.72含量逐渐降低,WO2含量逐渐升高,并且在C/WO3摩尔比为1.1时可得单相WO2。在整个碳热还原过程中,颗粒状WO3优先与蜂窝状活性炭充分接触并均匀混合。随着反应时间的增加,两者间开始进行热量传输并发生反应生成柱状WO2.72。之后,柱状WO2.72再进一步被还原成椭圆形WO2。并据此得出了制备分散性良好WO2的最佳条件:还原温度为1050 ℃,C/WO3摩尔比为1.1,反应时间为90 min。

WO2  /  WO3  /  碳热还原  /  物相转变  /  形貌演变  /  基础研究

WO2 is the important intermediate product during the carbothermal reduction of WO3 to WC, and the systematical analysis of the reduction behavior of WO3 to WO2 has a significant role on the efficient preparation of WC. Reaction behavior of carbothermal reduction of WO3 to WO2 was investigated with adaptation of thermogravimetric (TG), X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and thermodynamic calculation technologies. Influences of different parameters, such as reduction temperature, C/WO3 molar ratio, and reaction time, on the phase transition and morphological evolution during the process were considered. Results of non-isothermal reduction experiment from room temperature to 1200 ℃ showed that WO3 was preferentially reduced into WO2.72, then to WO2, and finally to metallic W. Phase transition law agreed well with thermodynamic theoretical calculation result. In the range of 1000 to 1050 ℃, with the increase of C/WO3 molar ratio, the relative content of WO2.72 in the reaction product gradually decreased, while that of WO2 increased. Single-phase WO2 can be prepared at the C/WO3 molar ratio of 1.1. However, when the C/WO3 molar ratio increased to 1.2, W formed due to the excess C. During the whole carbothermal reduction process, granular WO3 was first in contact with honeycomb activated carbon. As the increase of reaction time, heat transfer process began and then chemical reaction between the two reactants occurred to form columnar WO2.72. Subsequently, the columnar WO2.72 was further reduced into elliptical WO2. Based on experimental results, the optimal conditions for preparing well-dispersed WO2 were determined as follows: reduction temperature of 1050 ℃, C/WO3 molar ratio of 1.1, and reaction time of 90 min.

WO2  /  WO3  /  carbothermal reduction  /  phase transition  /  morphology evolution  /  fundamental research
杨春华, 张宇龙, 王璐, 朱爱国. 碳热还原WO3制备WO2基础研究. 铜业工程, 2026 , (3) : 95 -103 . DOI: 10.3969/j.issn.1009-3842.2026.03.011
Chunhua Yang, Yulong Zhang, Lu Wang, Aiguo Zhu. Fundamental Research on Carbothermal Reduction of WO3 to Prepare WO2[J]. Copper Engineering, 2026 , (3) : 95 -103 . DOI: 10.3969/j.issn.1009-3842.2026.03.011

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doi: 10.3969/j.issn.1009-3842.2026.03.011
  • 接收时间:2025-09-28
  • 首发时间:2026-09-08
  • 出版时间:2026-06-28
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  • 收稿日期:2025-09-28
  • 修回日期:2025-12-19
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    1.泰州伍伦肱智能科技有限公司,江苏 泰州 225502
    2.武汉科技大学 钢铁冶金及资源利用教育部重点实验室,湖北 武汉 430081
    3.江苏省安全生产宣传教育中心,江苏 南京 210042

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王璐,副教授,E-mail:
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2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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