首页> 外文期刊>Journal of Applied Polymer Science >Synthesis and properties of high oil-absorbent 4-tert-butylstyrene-EPDM-divinylbenzene graft terpolymer
【24h】

Synthesis and properties of high oil-absorbent 4-tert-butylstyrene-EPDM-divinylbenzene graft terpolymer

机译:高吸油性4-叔丁基苯乙烯-EPDM-二乙烯基苯接枝三元共聚物的合成与性能

获取原文
获取原文并翻译 | 示例
           

摘要

The graft crosslinking polymerization of 4-tent-butylstyrene (tBS) and divinylbenzene (DVB) onto ethylene-propylene-diene (EPDM) was carried out in toluene by using benzoyl peroxide (BPO) as an initiator. The synthesized graft terpolymer, tBS-EPDM-DVB (PBED), was extracted with tetrahydrofuran (THF) into gel (called as PBED I) and sol, and then they were identified by infrared (IR) spectroscopy. The effects of solvent amount, molar ratio of DVB to tBS, EPDM content, initiator concentration, reaction temperature, and reaction time on the graft crosslinking polymerization were examined. Among them, solvent amount and molar ratio of DVB to tBS were the important factors for this reaction system. Maximum oil absorbency of PBED I was 84.0 g/g but its oil-absorption kinetic rate was very low. Sol PBED can be reused as oil absorbent (named as PBED II) through photocrosslinking by ultraviolet light irradiation. Although the oil absorbencies of PBED II were lower than those of PBED I in most cases, their oil absorption kinetic rates were higher than oil absorbencies of PBED I. The highest value of oil absorbency of PBED II was 56.0 g/g. The thermal stability of PBED I was studied by TGA. (C) 2002 Wiley Periodicals, Inc. [References: 26]
机译:通过使用过氧化苯甲酰(BPO)作为引发剂,在甲苯中进行了4-帐篷丁基苯乙烯(tBS)和二乙烯基苯(DVB)在乙烯-丙烯-二烯(EPDM)上的接枝交联聚合反应。将合成的接枝三元共聚物tBS-EPDM-DVB(PBED)用四氢呋喃(THF)萃取到凝胶(称为PBED I)和溶胶中,然后通过红外(IR)光谱进行鉴定。考察了溶剂量,DVB与tBS的摩尔比,EPDM含量,引发剂浓度,反应温度和反应时间对接枝交联聚合的影响。其中,DVB与tBS的溶剂量和摩尔比是该反应体系的重要因素。 PBED I的最大吸油量为84.0 g / g,但其吸油动力学速率非常低。 Sol PBED可以通过紫外线照射进行光交联而重新用作吸油剂(命名为PBED II)。尽管在大多数情况下PBED II的吸油率低于PBED I,但它们的吸油动力学速率高于PBED I的吸油率。PBEDII的吸油率最高值为56.0 g / g。 TGA研究了PBED I的热稳定性。 (C)2002 Wiley Periodicals,Inc. [参考:26]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号