Zr4+ and glutaraldehyde cross-linked polyethyleneimine functionalized chitosan composite: Synthesis, characterization, Cr(VI) adsorption performance, mechanism and regeneration

吸附 壳聚糖 复合数 再生(生物学) 化学 戊二醛 机制(生物学) 表征(材料科学) 材料科学 化学工程 纳米技术 有机化学 色谱法 复合材料 细胞生物学 生物 哲学 工程类 认识论
作者
Chunzi Xu,Yunlan Xu,Dengjie Zhong,Haixing Chang,Jiaxin Mou,Hui Wang,Hongyu Shen
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:239: 124266-124266 被引量:20
标识
DOI:10.1016/j.ijbiomac.2023.124266
摘要

In order to improve the stability, electrostatic interaction and ion exchange ability of chitosan for Cr (VI) removal, it is an effective strategy to introduce polyvalent metal ions and polymers into chitosan molecular chain through crosslinking. In this paper, Zr4+ and glutaraldehyde crosslinked polyethyleneimine functionalized chitosan (CGPZ) composite was successfully synthesized and characterized by XRD, SEM, FTIR, BET, and XPS. The results showed that polyethyleneimine was successfully grafted onto chitosan by Schiff base reaction, while the appearance of ZrO and ZrN bonds verified the successful preparation of CGPZ. The monolayer maximum adsorption capacity of Cr(VI) by CGPZ was 593.72 mg g−1 at 298 K and t = 210 min. The removal efficiency of 100 mg L−1 Cr(VI) reached 95.7 %. The thermodynamic, isotherm and kinetic results show that the adsorption process of Cr (VI) by CGPZ is a spontaneous endothermic process controlled by entropy, which accords with Freundlich model and pseudo-second-order kinetic model. The regeneration experiments show that both HCl and NaOH can effectively desorb Cr(III) and Cr(VI) from the adsorbent surface, and the adsorbent has good acid-base resistance and regeneration performance. The removal of Cr(VI) mainly involves electrostatic attraction, ion exchange, reduction and complexation. CGPZ can synergistically adsorb Cr(VI) by electrostatic interaction of -NH2/-C=N and ion exchange of Cl− ion in the center of Zr, then reduce Cr(VI) to Cr(III) (45.4 % at pH = 2.0) by the -OH group on its surface, and chelate Cr(III) through COO- and -NH- groups.
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