The experiment of injection molding, Dais-simulating test, morphological structure investigation(Scanning Electron Microscopy, SEM),X-ray photoelectron spectroscopy(XPS)were performed on mini-automobile spherical seat...The experiment of injection molding, Dais-simulating test, morphological structure investigation(Scanning Electron Microscopy, SEM),X-ray photoelectron spectroscopy(XPS)were performed on mini-automobile spherical seat which was made of thermoplastic polyester elastomer(TPEE)and oiled polyoxymethylene(POM),respectively. The friction-wear properties between the frictionl pair of polymer spherical seat and metallic(iron)spherical pin were studied. The test results indicate that the antifriction property of TPEE is superior to that of POM, while its surface chemical effect is inferior to that of POM.展开更多
Block copolymers are marked by alternation of hard blocks and soft blocks, whereby the hard blocks are believed to form crystalline domains in non-crystalline matrix formed by aggregation of the soft blocks and a frac...Block copolymers are marked by alternation of hard blocks and soft blocks, whereby the hard blocks are believed to form crystalline domains in non-crystalline matrix formed by aggregation of the soft blocks and a fraction of the hard blocks escaping crystallization. On the basis of this two-phase model a number of studies has been made varying the nature and length of hard and soft blocks. After reviewing some papers published in this field, it may be concluded that the system in which properties of thermoplastic elastomers are exhibited can be generally divided into three catalogues, they are polyurethane, polyether-ester, polyesteramide elastomers. Structure-property relationship of these thermoplastic elastomers are given in this paper.展开更多
For practicable elastomeric polyethylene,achieving high catalyst thermal stability and activity,along with precise control of polymer properties such as branching density,molecular weights,and distribution,is crucial ...For practicable elastomeric polyethylene,achieving high catalyst thermal stability and activity,along with precise control of polymer properties such as branching density,molecular weights,and distribution,is crucial but challenging.In this study,two sets of symmetricalα-diimine nickel complexes,each comprising four nickel bromide or chloride complexes,were synthesized and investigated their performance for ethylene polymerization under various reaction conditions.Upon activation with either Et2AlCl or MMAO cocatalysts,these complexes displayed not only high activity but also generated high molecular weight polyethylenes with controlled polydispersity and a substantial number of branches.The catalyst with the least steric hindrance displayed the remarkable high activity(up to 1.2×10^(7) g·mol^(-1)·h^(-1)).Notably,nickel bromides demonstrated higher activity compared to their chloride counterparts.The investigation into the effect of reaction temperature on catalytic performance revealed that NiBrMe-MMAO system displayed high thermal stability(activity up to 2.51×10^(6) g·mol^(-1)·h^(-1) at 100℃)and consistently yielded high polymer molecular weights with narrow polydispersity over a broad temperature range of 30-100℃.Of significant note,mechanical analysis of the resulting polyethylene demonstrated excellent ultimate tensile strength and high strain at break.Particularly,the polyethylene sample prepared at 100℃exhibited ultimate tensile strength up to 10 MPa with 1863%maximum strain at break and a strain recovery of up to 54.9%after ten cycles at a fixed strain of 300%,indicating excellent material properties of prepared thermoplastic polyethylene elastomers(TPE).展开更多
Abstract Biodegradable poly（ether-imide-ester） elasto- mers were synthesized from succinic acid, 1,4-butanediol, polyethylene glycol 1000 and N＇,N-bis（2-carboxyethyl）- pyromellitimide which was derived from pyrom...Abstract Biodegradable poly（ether-imide-ester） elasto- mers were synthesized from succinic acid, 1,4-butanediol, polyethylene glycol 1000 and N＇,N-bis（2-carboxyethyl）- pyromellitimide which was derived from pyromellitic dianhydride and glycine. The chemical structures, crystal- linities, thermal stabilities, mechanical properties, hydro- philicities and biodegradabilities of these elastomers were investigated. The hard segments of the linear aliphatic poly （ether-ester） exhibited monoclinic chain packing. Increas- ing the amount of aromatic bisimide moieties in the poly （ether-ester） reduced the crystallinity of the material and improved the thermal stability and tensile strength of the elastomers. In addition, introducing a suitable amount of aromatic bisimide moieties into the poly（ether-ester） backbones endowed the elastomers with improved biode- gradability but too many aromatic bisimide groups reduced the biodegradability of the elastomers.展开更多
基金FundedbyKeyScientificandTechnologicalProjectofHubeiProvince (No .96 1 0 2 1 70 94 )
文摘The experiment of injection molding, Dais-simulating test, morphological structure investigation(Scanning Electron Microscopy, SEM),X-ray photoelectron spectroscopy(XPS)were performed on mini-automobile spherical seat which was made of thermoplastic polyester elastomer(TPEE)and oiled polyoxymethylene(POM),respectively. The friction-wear properties between the frictionl pair of polymer spherical seat and metallic(iron)spherical pin were studied. The test results indicate that the antifriction property of TPEE is superior to that of POM, while its surface chemical effect is inferior to that of POM.
文摘Block copolymers are marked by alternation of hard blocks and soft blocks, whereby the hard blocks are believed to form crystalline domains in non-crystalline matrix formed by aggregation of the soft blocks and a fraction of the hard blocks escaping crystallization. On the basis of this two-phase model a number of studies has been made varying the nature and length of hard and soft blocks. After reviewing some papers published in this field, it may be concluded that the system in which properties of thermoplastic elastomers are exhibited can be generally divided into three catalogues, they are polyurethane, polyether-ester, polyesteramide elastomers. Structure-property relationship of these thermoplastic elastomers are given in this paper.
基金This work was financially supported by the Chemistry and Chemical Engineering Guangdong Laboratory(Nos.2111018 and 2132012)Q.M.would like to express gratitude towards the Foreign Youth Talent Program(No.QN2022030008L)for their support.
文摘For practicable elastomeric polyethylene,achieving high catalyst thermal stability and activity,along with precise control of polymer properties such as branching density,molecular weights,and distribution,is crucial but challenging.In this study,two sets of symmetricalα-diimine nickel complexes,each comprising four nickel bromide or chloride complexes,were synthesized and investigated their performance for ethylene polymerization under various reaction conditions.Upon activation with either Et2AlCl or MMAO cocatalysts,these complexes displayed not only high activity but also generated high molecular weight polyethylenes with controlled polydispersity and a substantial number of branches.The catalyst with the least steric hindrance displayed the remarkable high activity(up to 1.2×10^(7) g·mol^(-1)·h^(-1)).Notably,nickel bromides demonstrated higher activity compared to their chloride counterparts.The investigation into the effect of reaction temperature on catalytic performance revealed that NiBrMe-MMAO system displayed high thermal stability(activity up to 2.51×10^(6) g·mol^(-1)·h^(-1) at 100℃)and consistently yielded high polymer molecular weights with narrow polydispersity over a broad temperature range of 30-100℃.Of significant note,mechanical analysis of the resulting polyethylene demonstrated excellent ultimate tensile strength and high strain at break.Particularly,the polyethylene sample prepared at 100℃exhibited ultimate tensile strength up to 10 MPa with 1863%maximum strain at break and a strain recovery of up to 54.9%after ten cycles at a fixed strain of 300%,indicating excellent material properties of prepared thermoplastic polyethylene elastomers(TPE).
文摘Abstract Biodegradable poly（ether-imide-ester） elasto- mers were synthesized from succinic acid, 1,4-butanediol, polyethylene glycol 1000 and N＇,N-bis（2-carboxyethyl）- pyromellitimide which was derived from pyromellitic dianhydride and glycine. The chemical structures, crystal- linities, thermal stabilities, mechanical properties, hydro- philicities and biodegradabilities of these elastomers were investigated. The hard segments of the linear aliphatic poly （ether-ester） exhibited monoclinic chain packing. Increas- ing the amount of aromatic bisimide moieties in the poly （ether-ester） reduced the crystallinity of the material and improved the thermal stability and tensile strength of the elastomers. In addition, introducing a suitable amount of aromatic bisimide moieties into the poly（ether-ester） backbones endowed the elastomers with improved biode- gradability but too many aromatic bisimide groups reduced the biodegradability of the elastomers.
