Role of polymer network and gelation kinetics on the mechanical properties and adsorption capacity of chitosan hydrogels for dye removal

被引:22
作者
de Luna, Martina Salzano [1 ,2 ]
Altobelli, Rosaria [1 ]
Gioiella, Lucia [1 ]
Castaldo, Rachele [1 ,3 ]
Scherillo, Giuseppe [1 ]
Filippone, Giovanni [1 ]
机构
[1] Univ Naples Federico II, Dept Chem Mat & Prod Engn INSTM Consortium UdR Na, Piazzale Tecchio 80, I-80125 Naples, Italy
[2] Natl Res Council Italy UoS Napoli Portici, Inst Polymers Composites & Biomat, Piazzale E Fermi 1, I-80055 Portici, Naples, Italy
[3] Natl Res Council Italy Headquarter, Inst Polymers Composites & Biomat, Via Campi Flegrei 34, I-80078 Pozzuoli, Naples, Italy
关键词
dye adsorption; hydrogels; mechanical properties; rheology; structure-property relations; INDIGO CARMINE DYE; AQUEOUS-SOLUTIONS; WASTE-WATER; FOOD DYES; DERIVATIVES; ADSORBENTS; FILMS; COMPOSITE;
D O I
10.1002/polb.24436
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Chitosan (CS) hydrogels are receiving growing attention as adsorbents for water purification purposes. The conditions of preparation of this class of materials play a crucial in the determination of their performances; however, this aspect is often neglected in the literature. In this study, we deal with this issue, focusing on the structure-property relationships of CS hydrogels obtained by phase inversion method. We show that the concentration of the starting solution determines the density and strength of intermolecular interactions, and that the gelation kinetics dictates the hydrogel structure at the microscale. Consequently, even subtle changes in the preparation protocol can cause significant differences in the performances of CS hydrogels in terms of mechanical properties and dye adsorption capacity. The observed trends are often neither trivial nor monotonic. Nonetheless, we demonstrate that they can be interpreted looking at the CS network structure, which can be inferred by rheological measurements. (c) 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017, 55, 1843-1849
引用
收藏
页码:1843 / 1849
页数:7
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