期刊
GELS
卷 8, 期 9, 页码 -出版社
MDPI
DOI: 10.3390/gels8090546
关键词
cationic enteromorpha polysaccharide; hydrogel; structural; adsorption
资金
- Natural Science Foundation of Tianjin City [20JCYBJC00830]
- Basic Research Fund of The Central Public Welfare Scientific Research Institutions [K-JBYWF-2019-ZT02, K-JBYWF-2019-T06]
In this study, EPS polysaccharides were extracted from Enteromorpha prolifera and cationic modification was performed to obtain CAEPS hydrogel. The structural characteristics of EPS and CAEPS-based hydrogel were analyzed, showing that CAEPS hydrogels have higher porosity, apparent density, and hydrophilicity compared to EPS hydrogels. The adsorption mechanism of the hydrogels on three typical pollutants in water was studied, with the results indicating that the adsorption isotherms of both hydrogels followed the Langmuir model and the adsorption capacity of CAEPS hydrogels was higher than that of EPS hydrogels.
Hydrogels with polysaccharides as high polymer substrates have surprising advantages in wastewater treatment with complex components. Therefore, in this study, polysaccharides named EPS were extracted from Enteromorpha prolifera, a coastal pollutant with a wide range of sources, and cationic modification was performed to obtain CAEPS, the hydrogel with a double network structure was prepared based on EPS and CAEPS. Meanwhile, the structural characteristic of EPS and CAEPS-based hydrogel were identified by HPLC, AFM, FT-IR, TGA, SEM-EDS, Pore size distribution, and WCA, which showed that the porosity, apparent (skeletal) density, and hydrophilicity of CAEPS-hydrogels. We used nonlinear isotherms to uncover the adsorption mechanism of hydrogel applied to the water environment containing three typical pollutants (Methylene blue, Cefuroxime, and Cr (VI)). The results showed that the adsorption isotherm of the two hydrogels fit the Langmuir isotherm model, which indicated the monolayer adsorption of the pollution factor onto EPS- and CAEPS-hydrogels. The maximum adsorption capacities of CAEPS-hydrogels were higher than EPS-hydrogels, which indicated the microstructure and adsorption performance of the CAEPS-hydrogel are strengthened.
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