对羧基苯基氨基马来酰亚胺-g-醋酸纤维素/ZrO2纳米复合海水淡化膜的合成与表征

IF 4.3 4区 环境科学与生态学 Q2 ENGINEERING, ENVIRONMENTAL
Water Reuse Pub Date : 2023-07-17 DOI:10.2166/wrd.2023.036
A. Abdel-Naby, Bushra A. Alabdullatif, Sarah Aldulaijan, Yanallah Alqarni
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引用次数: 0

摘要

对羧基苯基氨基马来酰亚胺(CHM)与醋酸纤维素(CA)反应生成改性醋酸纤维素聚合物(MCA),并用紫外/可见光谱、1H NMR和13C NMR对其进行了表征。反应的活性位点为(CHM)的-NH基团和CA的OAc基团。以过氧化苯甲酰为引发剂,将(CHM)接枝在CA的主链上建立支链。1H NMR和13C NMR结果表明,聚合物基体中存在(CHM)基团。采用相变技术制备了(CA-g-CHM) ZrO2薄膜。讨论了ZrO2含量对水通量的影响。利用SEM/EDS对膜的内容物和形态进行了表征。膜的形貌显示接枝部分,能谱分析证实了聚合物基质中存在氮原子。热重(TGA)测试结果表明,该膜具有较高的热稳定性,可以调节膜在脱盐过程中的性能。脱盐试验表明,膜对NaCl盐有脱盐作用,EDS和1H NMR结果表明膜对NaCl盐有脱盐作用。该膜具有良好的抗菌和抗真菌性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and characterization of p-carboxy phenyl amino maleimide-g-cellulose acetate/ZrO2 nanocomposite membrane for water desalination
The reaction of p-carboxy phenyl amino maleimide (CHM) with cellulose acetate (CA), led to the formation of a modified cellulose acetate polymer (MCA), which was characterized by UV/Vis, 1H NMR, and 13C NMR. The active sites of the reaction were the –NH group of (CHM) and the OAc of CA. CA was grafted with (CHM) to build branches on its main chains, using benzoyl peroxide as an initiator. The results of 1H NMR and 13C NMR revealed the presence of (CHM) moieties inside the polymeric matrix. The (CA-g-CHM) ZrO2 was fabricated into a membrane, using a phase inversion technique. The effect of ZrO2 content on the water flux was discussed. The SEM/EDS was also used to characterize the membrane contents and morphology. The morphology of the membrane showed the grafted parts and the EDS confirmed the presence of nitrogen atoms in the polymeric matrix. The thermogravimetry (TGA) results showed that the membrane exhibited high thermal stability which would adjust the membrane for the desalination process. The desalination test indicated the removal of NaCl salt by the membrane, as shown by the EDS and 1H NMR spectroscopy results. The membrane exhibited good antibacterial and antifungal properties.
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来源期刊
Water Reuse
Water Reuse Multiple-
CiteScore
6.20
自引率
8.90%
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0
审稿时长
7 weeks
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