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Use of TBzTD as Noncarcinogenic Accelerator for ENR/SiO2 Nanocomposites: Cured Characteristics, Mechanical Properties, Thermal Behaviors, and Oil Resistance

机译:使用TBZTD作为ENR / SiO2纳米复合材料的非可通癌促进剂:固化特性,机械性能,热行为和耐油性

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摘要

This study reported the use of tetrabenzylthiuram disulphide (TBzTD) as a noncarcinogenic accelerator in a traditional sulfur curing system of epoxidized natural rubber (ENR)/nanosilica (nSiO2) composites. ENR used in this work was synthesized via in situ epoxidation of natural rubber (NR) in the presence of performic acid generated from the reaction of formic acid and hydrogen peroxide at 50°C for 8 h to acquire the epoxide content of about 40 mol%. Accordingly, the resulting ENR was referred to as ENR 40. The curing characteristics, mechanical properties, thermal behaviors, dynamic mechanical properties, and oil resistance of ENR 40/nSiO2 nanocomposites filled with three loadings of nSiO2 (1, 2, and 3 parts per hundred parts of rubber) were investigated and compared with NR and neat ENR 40. The results revealed that the scorch and cure times of ENR 40/nSiO2 nanocomposites were slightly longer than those of NR but slightly shorter than those of ENR 40. The tensile properties and tear strength for both before and after aging of all ENR 40/nSiO2 nanocomposites were higher than those of ENR 40, while the glass transition temperature, storage modulus at −65°C, thermal stability, and oil resistance of ENR 40/nSiO2 nanocomposites were higher than those of NR and ENR 40.
机译:本研究报告说,在环氧化天然橡胶(ENR)/纳米硅(NSIO2)复合材料的传统硫固化体系中,使用四苄硫硫氨酰胺(TBZTD)作为非易生性促进剂。在该工作中使用的ENR通过在50℃的甲酸和过氧化氢的反应产生8小时的情况下通过原位环氧化通过天然橡胶(NR)的含量,以获得约40摩尔%的环氧化物含量。因此,所得的enR被称为ENR 40. enR 40 / NSIO2纳米复合材料的固化特性,机械性能,热行为,动态力学性能和耐油性填充有三个NSIO2(1,2和3份研究了一份橡胶)并与NR和整齐的恩恩40进行了比较。结果表明,ERN 40 / NSIO2纳米复合材料的烧焦和固化时间略高于NR,但略短于NR 40.拉伸性质在所有ENR 40 / NSIO2纳米复合材料的老化之前和之后的撕裂强度高于ENR 40,而玻璃化转变温度,储存量为-65℃,耐热稳定性和耐油性的耐磨性40 / NSIO2纳米复合材料高于NR和NR 40。

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