M. Davydova, A. R. Khaldeeva, A. Fedorova, M. Sokolova
{"title":"环氧氯丙烷橡胶硫化组促进剂的选择","authors":"M. Davydova, A. R. Khaldeeva, A. Fedorova, M. Sokolova","doi":"10.30791/1028-978x-2023-3-24-31","DOIUrl":null,"url":null,"abstract":"The effect of vulcanization accelerators on the structure and properties of rubbers based on Hydrin T6000 epichlorohydrin rubber has been studied. Mercaptobenzthiazole (MBT) in the amount of 1.5 pts.wt., tetramethylthiuram disulfide (TMTD) — 0.5 – 1.5 pst.wt. were used as accelerators and N,N’-diphenylguanidine (DPG) — 0.5 – 1.5 pst.wt., which represent a triple system of accelerators. The choice of accelerators is based on the possibility of obtaining a vulcanization spatial structure of different sulfide content: thiuram group accelerators promote the formation of mono-, disulfide bonds; guanidine — polysulfide bonds, and thiazole groups — from carbon-carbon to polysulfide with varying degrees of sulfide. According to the results of the study of physical and mechanical properties, the determination of the parameters of the spatial grid and the study of the dynamic behavior of rubber, differences were revealed due to the formation of a spatial structure with different types of cross-links and density. It is shown that rubber containing 1.5 pst. wt. MBT, 0.5 pst. wt. DFG and 0.5 – 1.0 pst.wt. TMTD due to the manifestation of a synergistic effect on the formation of a vulcanization network of a certain density and the ratio of poly-, di- and monosulfide cross-links. Thus, the use of a group of accelerators with different functional effects makes it possible to obtain vulcanizates with an optimal set of technological and operational properties.","PeriodicalId":20003,"journal":{"name":"Perspektivnye Materialy","volume":"42 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Choice of accelerators of the vulcanization group for rubbers based on epichlorohydrin rubber\",\"authors\":\"M. Davydova, A. R. Khaldeeva, A. Fedorova, M. Sokolova\",\"doi\":\"10.30791/1028-978x-2023-3-24-31\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The effect of vulcanization accelerators on the structure and properties of rubbers based on Hydrin T6000 epichlorohydrin rubber has been studied. Mercaptobenzthiazole (MBT) in the amount of 1.5 pts.wt., tetramethylthiuram disulfide (TMTD) — 0.5 – 1.5 pst.wt. were used as accelerators and N,N’-diphenylguanidine (DPG) — 0.5 – 1.5 pst.wt., which represent a triple system of accelerators. The choice of accelerators is based on the possibility of obtaining a vulcanization spatial structure of different sulfide content: thiuram group accelerators promote the formation of mono-, disulfide bonds; guanidine — polysulfide bonds, and thiazole groups — from carbon-carbon to polysulfide with varying degrees of sulfide. According to the results of the study of physical and mechanical properties, the determination of the parameters of the spatial grid and the study of the dynamic behavior of rubber, differences were revealed due to the formation of a spatial structure with different types of cross-links and density. It is shown that rubber containing 1.5 pst. wt. MBT, 0.5 pst. wt. DFG and 0.5 – 1.0 pst.wt. TMTD due to the manifestation of a synergistic effect on the formation of a vulcanization network of a certain density and the ratio of poly-, di- and monosulfide cross-links. Thus, the use of a group of accelerators with different functional effects makes it possible to obtain vulcanizates with an optimal set of technological and operational properties.\",\"PeriodicalId\":20003,\"journal\":{\"name\":\"Perspektivnye Materialy\",\"volume\":\"42 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Perspektivnye Materialy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.30791/1028-978x-2023-3-24-31\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Perspektivnye Materialy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30791/1028-978x-2023-3-24-31","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Choice of accelerators of the vulcanization group for rubbers based on epichlorohydrin rubber
The effect of vulcanization accelerators on the structure and properties of rubbers based on Hydrin T6000 epichlorohydrin rubber has been studied. Mercaptobenzthiazole (MBT) in the amount of 1.5 pts.wt., tetramethylthiuram disulfide (TMTD) — 0.5 – 1.5 pst.wt. were used as accelerators and N,N’-diphenylguanidine (DPG) — 0.5 – 1.5 pst.wt., which represent a triple system of accelerators. The choice of accelerators is based on the possibility of obtaining a vulcanization spatial structure of different sulfide content: thiuram group accelerators promote the formation of mono-, disulfide bonds; guanidine — polysulfide bonds, and thiazole groups — from carbon-carbon to polysulfide with varying degrees of sulfide. According to the results of the study of physical and mechanical properties, the determination of the parameters of the spatial grid and the study of the dynamic behavior of rubber, differences were revealed due to the formation of a spatial structure with different types of cross-links and density. It is shown that rubber containing 1.5 pst. wt. MBT, 0.5 pst. wt. DFG and 0.5 – 1.0 pst.wt. TMTD due to the manifestation of a synergistic effect on the formation of a vulcanization network of a certain density and the ratio of poly-, di- and monosulfide cross-links. Thus, the use of a group of accelerators with different functional effects makes it possible to obtain vulcanizates with an optimal set of technological and operational properties.