W和b4c改性石英纤维/硼酚醛树脂陶瓷复合材料的高温抗弯强度、微观结构和相演化

He Ding, Sige Huang, Xiaofan Liu, Zongyi Deng, Minxian Shi, Zhixiong Huang, Yue Wu
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The results showed that the introduced refractory metal tungsten and the boron carbide can react to form tungsten borides and tungsten carbides at high temperature, and form a ceramic layer on the surface of the composite, which can fill the defects caused by pyrolysis of matrix and improve the high temperature performance of the composite. When the content of boron carbide was 10wt% and the content of tungsten powder was 30wt%, the flexural strength of the composite before and after heat treatment at 1200 °C were increased by 54.6% and 30.2% respectively compared with that without filler.Keywords: Refractory metalsBoron carbideBoron phenolic resinThermal protectionCeramizable compositesDisclaimerAs a service to authors and researchers we are providing this version of an accepted manuscript (AM). Copyediting, typesetting, and review of the resulting proofs will be undertaken on this manuscript before final publication of the Version of Record (VoR). During production and pre-press, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal relate to these versions also. Disclosure statementThe authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paperTable 1 Formulas of ceramizable compositesDownload CSVDisplay TableTable 2 Thermal decomposition properties of compositesDownload CSVDisplay TableFigure 1 Curing process curves of ceramizable phenolic resin compositesDisplay full sizeFigure 2 TGA and DTGA curves of the composites in air atmosphere (a: TGA curves; b: DTGA curves)Display full sizeFigure 3 Flexural strength of the composites treated at different temperaturesDisplay full sizeFigure 4 Surface morphology of the composites after being treated at different temperatures (a:600 °C;b:1000 °C)Display full sizeFigure 5 Surface morphology of B0W0 after being treated at 1400 °C and the corresponding EDS mapping results.Display full sizeFigure 6 Surface morphology of B0W30 after being treated at 1400 °C and the corresponding EDS mapping results.Display full sizeDisplay full sizeFigure 7 Surface morphology of B10W30 after being treated at 1400 °C and the corresponding EDS mapping results.Display full sizeFigure 8 XRD patterns of cracked products of the composites after being treated at various temperatures (a:B0W30;b:B10W30)Display full sizeFigure 9 Gibbs free energy change curves of the reactions. (reaction 1: the oxidation reaction of W; reaction 8 : the oxidation reaction of boron carbide)Display full sizeFigure 10 Surface morphologies of the composites after being treated at various temperatures (a: room temperature;b:600 °C;c:800 °C;d:1000 °C;e:1200 °C;f:1400 °C)Display full sizeFigure 11 Macroscopic side morphologies of the composite materials after being treated at various temperatures (a: 1400 °C;b:1200 °C;c:1000 °C;d:800 °C;e:600 °C;f:room temperature)Display full sizeFigure 12 Display full sizeDisplay full sizeAdditional informationFundingThis work was funded by the Independent Innovation Projects of the Hubei Longzhong Laboratory (2022ZZ-08), the Fundamental Research Funds for the Central Universities (2023-CL-B1-08) and the Industrialization Project of the Xiangyang Technology Transfer Center of Wuhan University of Technology (WXCJ-20220008).","PeriodicalId":16285,"journal":{"name":"Journal of Macromolecular Science, Part B","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"High temperature flexural strength, microstructure, and phase evolution of quartz fiber/boron phenolic resin ceramizable composite modified with W and B <sub>4</sub> C\",\"authors\":\"He Ding, Sige Huang, Xiaofan Liu, Zongyi Deng, Minxian Shi, Zhixiong Huang, Yue Wu\",\"doi\":\"10.1080/00222348.2023.2259172\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract:In order to investigate the effect of refractory metal on the high temperature properties of phenolic resin matrix composites, modified quartz fiber reinforced ceramizable composites were prepared by a molding process with a refractory component, tungsten, as the functional component and boron carbide as the ceramic forming agent. 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引用次数: 0

摘要

摘要:为研究难熔金属对酚醛树脂基复合材料高温性能的影响,以难熔成分钨为功能组分,碳化硼为陶瓷成型剂,采用成型工艺制备了改性石英纤维增强陶化复合材料。研究了碳化硼和碳化钨对复合材料耐热性能的影响。结果表明:引入的难熔金属钨与碳化硼在高温下反应生成碳化钨和碳化钨,并在复合材料表面形成陶瓷层,可以填补基体热解产生的缺陷,提高复合材料的高温性能。当碳化硼含量为10wt%,钨粉含量为30wt%时,复合材料在1200℃热处理前后的抗折强度比未添加填料的复合材料分别提高了54.6%和30.2%。关键词:难熔金属硼碳硼酚树脂热保护陶化复合材料免责声明作为对作者和研究人员的服务,我们提供这个版本的接受手稿(AM)。在最终出版版本记录(VoR)之前,将对该手稿进行编辑、排版和审查。在制作和印前,可能会发现可能影响内容的错误,所有适用于期刊的法律免责声明也与这些版本有关。公开声明:作者声明,他们没有已知的竞争经济利益或个人关系,可能会影响本文所报道的工作。表1可陶化复合材料的配方下载csv显示表2复合材料的热分解性能下载csv显示表图1可陶化酚醛树脂复合材料的固化过程曲线显示完整尺寸图2复合材料在空气气氛中的TGA和DTGA曲线(a:TGA曲线;图4不同温度(a:600℃;b:1000℃)处理后的复合材料表面形貌图5 1400℃处理后的B0W0表面形貌及相应的EDS映射结果。图6 1400℃处理后的B0W30表面形貌及相应的EDS测绘结果图7 1400℃处理后的B10W30表面形貌及相应的EDS测绘结果。图8不同温度下复合材料裂解产物的XRD图谱(a:B0W30;b:B10W30)图9反应的吉布斯自由能变化曲线(反应1:W的氧化反应;图10不同温度(a:室温;b:600℃;C:800℃;d:1000℃;e:1200℃;f:1400℃)处理后的复合材料表面形貌图11不同温度(a: 1400℃;b:1200℃;C:1000℃;d:800℃;e:600℃;f:本工作由湖北省隆中实验室自主创新专项(2022ZZ-08)、中央高校基本科研业务费专项(2023-CL-B1-08)和武汉理工大学襄阳技术转移中心产业化项目(WXCJ-20220008)资助。
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High temperature flexural strength, microstructure, and phase evolution of quartz fiber/boron phenolic resin ceramizable composite modified with W and B 4 C
Abstract:In order to investigate the effect of refractory metal on the high temperature properties of phenolic resin matrix composites, modified quartz fiber reinforced ceramizable composites were prepared by a molding process with a refractory component, tungsten, as the functional component and boron carbide as the ceramic forming agent. The effects of the tungsten and the boron carbide on the heat resistance of the composite were investigated. The results showed that the introduced refractory metal tungsten and the boron carbide can react to form tungsten borides and tungsten carbides at high temperature, and form a ceramic layer on the surface of the composite, which can fill the defects caused by pyrolysis of matrix and improve the high temperature performance of the composite. When the content of boron carbide was 10wt% and the content of tungsten powder was 30wt%, the flexural strength of the composite before and after heat treatment at 1200 °C were increased by 54.6% and 30.2% respectively compared with that without filler.Keywords: Refractory metalsBoron carbideBoron phenolic resinThermal protectionCeramizable compositesDisclaimerAs a service to authors and researchers we are providing this version of an accepted manuscript (AM). Copyediting, typesetting, and review of the resulting proofs will be undertaken on this manuscript before final publication of the Version of Record (VoR). During production and pre-press, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal relate to these versions also. Disclosure statementThe authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paperTable 1 Formulas of ceramizable compositesDownload CSVDisplay TableTable 2 Thermal decomposition properties of compositesDownload CSVDisplay TableFigure 1 Curing process curves of ceramizable phenolic resin compositesDisplay full sizeFigure 2 TGA and DTGA curves of the composites in air atmosphere (a: TGA curves; b: DTGA curves)Display full sizeFigure 3 Flexural strength of the composites treated at different temperaturesDisplay full sizeFigure 4 Surface morphology of the composites after being treated at different temperatures (a:600 °C;b:1000 °C)Display full sizeFigure 5 Surface morphology of B0W0 after being treated at 1400 °C and the corresponding EDS mapping results.Display full sizeFigure 6 Surface morphology of B0W30 after being treated at 1400 °C and the corresponding EDS mapping results.Display full sizeDisplay full sizeFigure 7 Surface morphology of B10W30 after being treated at 1400 °C and the corresponding EDS mapping results.Display full sizeFigure 8 XRD patterns of cracked products of the composites after being treated at various temperatures (a:B0W30;b:B10W30)Display full sizeFigure 9 Gibbs free energy change curves of the reactions. (reaction 1: the oxidation reaction of W; reaction 8 : the oxidation reaction of boron carbide)Display full sizeFigure 10 Surface morphologies of the composites after being treated at various temperatures (a: room temperature;b:600 °C;c:800 °C;d:1000 °C;e:1200 °C;f:1400 °C)Display full sizeFigure 11 Macroscopic side morphologies of the composite materials after being treated at various temperatures (a: 1400 °C;b:1200 °C;c:1000 °C;d:800 °C;e:600 °C;f:room temperature)Display full sizeFigure 12 Display full sizeDisplay full sizeAdditional informationFundingThis work was funded by the Independent Innovation Projects of the Hubei Longzhong Laboratory (2022ZZ-08), the Fundamental Research Funds for the Central Universities (2023-CL-B1-08) and the Industrialization Project of the Xiangyang Technology Transfer Center of Wuhan University of Technology (WXCJ-20220008).
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