Liu Hongxu, Xie Junhao, Hu Ziyi, Zhao Jingxuan, Wang Ruijia, Qi Yuchao, Sun Shulin
School of Chemical Engineering, Changchun University of Technology, Changchun 130012, China; Engineering Research Center of Synthetic Resin and Special Fiber, Ministry of Education, Changchun University of Technology, Changchun 130012, China.
School of Chemical Engineering, Changchun University of Technology, Changchun 130012, China; Engineering Research Center of Synthetic Resin and Special Fiber, Ministry of Education, Changchun University of Technology, Changchun 130012, China.
Carbohydr Polym. 2024 Jan 1;323:121467. doi: 10.1016/j.carbpol.2023.121467. Epub 2023 Oct 7.
This work obtained separation membranes with UV-cleaning performance by adding TiO-g-CS/CNTs photocatalyst to the PVDF. The positively charged chitosan (CS) and negatively charged carboxylic carbon nanotube (CNTs-COOH) can be self-assembled into the bilayer structure on the surface of TiO particles through electrostatic attraction. The presence of many hydrophilic groups in CS and CNTs-COOH significantly improves the hydrophilicity of TiO-g-CS/CNTs-PVDF membrane, and helps TiO to be uniformly dispersed on the upper surface. TiO-g-CS/CNTs promote the change of pore structure and expand the flux of the modified membrane to 4.5 times that of pure PVDF. Zeta potential demonstrates that the TiO-g-CS particles successfully attracted CNTs in the PVDF matrix, and the membrane surface was still positively charged. Thus, the combined effect of the positively charged TiO-g-CS and the highly adsorbed CNTs enhanced the retention of the contaminants. More importantly, there is a charge transfer between the grafted CS and TiO interface to obtain a broader light absorption band. The excitation carriers provided by CNTs significantly contribute to the photocatalytic performance after transfer between TiO and CS; thus, TiO-g-CS/CNTs-PVDF produces higher photocatalytic activity for dye molecules (degradation rate > 97 %).
通过将TiO-g-CS/CNTs光催化剂添加到聚偏氟乙烯(PVDF)中,这项工作获得了具有紫外线清洁性能的分离膜。带正电荷的壳聚糖(CS)和带负电荷的羧基碳纳米管(CNTs-COOH)可以通过静电吸引自组装成TiO颗粒表面的双层结构。CS和CNTs-COOH中许多亲水性基团的存在显著提高了TiO-g-CS/CNTs-PVDF膜的亲水性,并有助于TiO均匀地分散在上表面。TiO-g-CS/CNTs促进了孔结构的变化,并将改性膜的通量扩大到纯PVDF的4.5倍。zeta电位表明,TiO-g-CS颗粒成功地在PVDF基质中吸引了CNTs,并且膜表面仍然带正电。因此,带正电的TiO-g-CS和高度吸附的CNTs的联合作用增强了对污染物的截留。更重要的是,接枝的CS和TiO界面之间存在电荷转移,以获得更宽的光吸收带。碳纳米管提供的激发载流子在TiO和CS之间转移后对光催化性能有显著贡献;因此,TiO-g-CS/CNTs-PVDF对染料分子产生更高的光催化活性(降解率>97%)。