{"title":"粘土/SEBS插层复合材料的制备及性能研究","authors":"T. Yamaguchi, E. Yamada","doi":"10.2324/EJSM.2.1","DOIUrl":null,"url":null,"abstract":"Clay/polystyrene-b-poly(ethylene-co-butylene)-b-polystyrene triblock copolymer (SEBS) intercalated composites were prepared by melt-blending. The clays were a pristine montmorillonite (Mt) and three organically modified montmorillonites (organo-Mts) with different amounts of distearyldimethylammonium (D18) cation. The amounts of D18 were 50, 70 and 100% of the cation exchange capacity (denoted as D18Mt(50), D18Mt(70) and D18Mt(100), respectively). The clay/SEBS composites were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction analysis (XRD). The dynamic mechanical analysis (DMA) and the tensile properties were also examined.The size of agglomerated clay particles decreased with the increasing amount of D18. The FE-SEM image of D18Mt(100)/SEBS revealed that the clay particles were dispersed at the sub-μm level (100–500 nm). The XRD patterns suggested that the SEBS chains were inserted into the interlayers of the organo-Mts. The DMA curves indicated that the addition of the organo-Mts produced an increase in the storage modulus in the rubbery plateau region, but a slight decrease in the glass transition temperature of the polystyrene domains. The tensile properties of the organo-Mt/SEBS composites were higher than those of the unmodified Mt/SEBS. D18Mt(100)/SEBS displayed an improved tensile modulus, tear strength and hardness compared to pure SEBS, without sacrificing the tensile strength and elongation at break.","PeriodicalId":11628,"journal":{"name":"E-journal of Soft Materials","volume":"13 1","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Preparation and Properties of Clay/SEBS Intercalated Composites\",\"authors\":\"T. Yamaguchi, E. Yamada\",\"doi\":\"10.2324/EJSM.2.1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Clay/polystyrene-b-poly(ethylene-co-butylene)-b-polystyrene triblock copolymer (SEBS) intercalated composites were prepared by melt-blending. The clays were a pristine montmorillonite (Mt) and three organically modified montmorillonites (organo-Mts) with different amounts of distearyldimethylammonium (D18) cation. The amounts of D18 were 50, 70 and 100% of the cation exchange capacity (denoted as D18Mt(50), D18Mt(70) and D18Mt(100), respectively). The clay/SEBS composites were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction analysis (XRD). The dynamic mechanical analysis (DMA) and the tensile properties were also examined.The size of agglomerated clay particles decreased with the increasing amount of D18. The FE-SEM image of D18Mt(100)/SEBS revealed that the clay particles were dispersed at the sub-μm level (100–500 nm). The XRD patterns suggested that the SEBS chains were inserted into the interlayers of the organo-Mts. The DMA curves indicated that the addition of the organo-Mts produced an increase in the storage modulus in the rubbery plateau region, but a slight decrease in the glass transition temperature of the polystyrene domains. The tensile properties of the organo-Mt/SEBS composites were higher than those of the unmodified Mt/SEBS. D18Mt(100)/SEBS displayed an improved tensile modulus, tear strength and hardness compared to pure SEBS, without sacrificing the tensile strength and elongation at break.\",\"PeriodicalId\":11628,\"journal\":{\"name\":\"E-journal of Soft Materials\",\"volume\":\"13 1\",\"pages\":\"1-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"E-journal of Soft Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2324/EJSM.2.1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"E-journal of Soft Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2324/EJSM.2.1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Preparation and Properties of Clay/SEBS Intercalated Composites
Clay/polystyrene-b-poly(ethylene-co-butylene)-b-polystyrene triblock copolymer (SEBS) intercalated composites were prepared by melt-blending. The clays were a pristine montmorillonite (Mt) and three organically modified montmorillonites (organo-Mts) with different amounts of distearyldimethylammonium (D18) cation. The amounts of D18 were 50, 70 and 100% of the cation exchange capacity (denoted as D18Mt(50), D18Mt(70) and D18Mt(100), respectively). The clay/SEBS composites were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction analysis (XRD). The dynamic mechanical analysis (DMA) and the tensile properties were also examined.The size of agglomerated clay particles decreased with the increasing amount of D18. The FE-SEM image of D18Mt(100)/SEBS revealed that the clay particles were dispersed at the sub-μm level (100–500 nm). The XRD patterns suggested that the SEBS chains were inserted into the interlayers of the organo-Mts. The DMA curves indicated that the addition of the organo-Mts produced an increase in the storage modulus in the rubbery plateau region, but a slight decrease in the glass transition temperature of the polystyrene domains. The tensile properties of the organo-Mt/SEBS composites were higher than those of the unmodified Mt/SEBS. D18Mt(100)/SEBS displayed an improved tensile modulus, tear strength and hardness compared to pure SEBS, without sacrificing the tensile strength and elongation at break.