Fast cost-effective synthesis of metal ions/biopolymer/silica composites by supramolecular hydrogels crosslink with superior tetracycline sorption performance

被引:8
|
作者
Qiao, Han [1 ,2 ]
Li, Binrui [2 ]
Hu, Shiwen [2 ]
Liu, Chongxuan [2 ]
机构
[1] Harbin Inst Technol, Sch Environm, Harbin 150090, Peoples R China
[2] Southern Univ Sci & Technol, Sch Environm Sci & Engn, State Environm Protect Key Lab Integrated Surface, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Tetracycline; Cu 3-CS 2-Si composites; Fast sorption kinetics; Broad working pH; Cu-O complexation; FUNCTIONALIZED MESOPOROUS SILICA; EFFECTIVE REMOVAL; AQUEOUS-SOLUTION; ADSORPTION; COMPLEXATION; ANTIBIOTICS; BEHAVIORS; NANOTUBES; KINETICS; SPONGE;
D O I
10.1016/j.chemosphere.2022.133821
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, a fast one-pot method was developed for the preparation of Cu/CS/Si ternary composites, which can efficiently remove antibiotic tetracycline from aqueous solutions. Our results demonstrated that the Cu and its content in the composites played a significant role in determining the physical properties and internal morphology of the Cu/CS/Si composites, which subsequently affected the efficiency of the composites for the sorptive removal of tetracycline. Among the studied composites, Cu3-CS2-Si materials had the largest sorption capacity for tetracycline (1076.7 mg/g) with a fast sorption kinetics (>99% in 30 min) under a broad working pH range (5-10). The results from the batch sorption experiments, together with spectroscopic and microscopic analyses, collectively indicated that Cu-tetracycline inner-sphere surface complexation through Cu-O bond was responsible for the tetracycline sorption on Cu3-CS2-Si. In addition, the Cu3-CS2-Si showed an excellent reusability in removing tetracycline. The desired sorption and reuse properties, coupled with the facile and costeffective synthesis method, indicated that Cu/CS/Si composites have a promising potential for the efficient removal of tetracycline from contaminated solutions.
引用
收藏
页数:9
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