首页> 外文期刊>Macromolecules >Synthesis and evaluation of photoactive polyethylene terephthalate-g-ethylmethacrylate based on waste PET
【24h】

Synthesis and evaluation of photoactive polyethylene terephthalate-g-ethylmethacrylate based on waste PET

机译:基于废旧PET的光敏性聚对苯二甲酸乙二醇酯-g-甲基丙烯酸乙酯的合成与评价

获取原文
获取原文并翻译 | 示例
           

摘要

Waste polyethylene terephthalate (PET) was grafted with ethyl methacrylate monomer (EMA) using potassium persulphate; (KJPS) as initiator in absence/ presence of anatase and N-doped titanium dioxide; (TiO2 and N-doped TiO2) to produce a photoactive grafted copolymer that can be used in water treatment. Effect of various concentrations of monomer and initiator on grafting yield (G%) and grafting efficiency (GE%) were investigated. The effect of added TiO2 and N-doped TiO2 during grafting of waste PET on the photocatalytic activity of the resulting copolymer was also investigated. FTIR, TGA and SEM techniques were employed to characterize the prepared samples. Results revealed that optimum G% and GE% were obtained upon applying monomer and initiator concentrations of 2 x 10~(-3) and 1.5 x 10~(-3) mol/L at 70 °C after 300 minutes. The photocatalytic activity of the prepared grafted PET copolymer was evaluated by investigating the degradation of methylene blue dye using the grafted copolymer as photocatalyst. The results showed that the grafted PET containing N-doped TiO2 gave the highest rate of photocatalytic degradation of methylene blue using solar energy as a source of irradiation.
机译:使用过硫酸钾将废弃的聚对苯二甲酸乙二醇酯(PET)与甲基丙烯酸乙酯单体(EMA)接枝; (KJPS)在不存在/存在锐钛矿和N掺杂的二氧化钛的情况下作为引发剂; (TiO2和N掺杂的TiO2)生成可用于水处理的光敏接枝共聚物。研究了不同浓度的单体和引发剂对接枝率(G%)和接枝效率(GE%)的影响。还研究了在废PET接枝过程中添加的TiO2和N掺杂的TiO2对所得共聚物的光催化活性的影响。 FTIR,TGA和SEM技术用于表征制备的样品。结果表明,在70分钟300分钟后,施加单体和引发剂浓度分别为2 x 10〜(-3)和1.5 x 10〜(-3)mol / L可获得最佳的G%和GE%。通过研究使用接枝共聚物作为光催化剂的亚甲基蓝染料的降解来评估制备的接枝PET共聚物的光催化活性。结果表明,以太阳能为辐照源,含N掺杂TiO2的接枝PET对亚甲基蓝的光催化降解率最高。

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