通过水包一氧化碳乳液形成的磺化水凝胶:抗生素去除的潜力。
Sulfonated Hydrogel Formed via CO-in-Water Emulsion: Potential in Antibiotic Removal.
作者信息
Xu Kaibo, Cao Liqin
机构信息
Key Laboratory of Oil and Gas Fine Chemicals, College of Chemistry, Ministry of Education & Xinjiang Uygur Autonomous Region, Xinjiang University, Urumqi 830017, China.
School of Science, Xihua University, Chengdu 610039, China.
出版信息
Gels. 2023 Aug 31;9(9):703. doi: 10.3390/gels9090703.
Herein, a green, carbon dioxide-in-water high-internal-phase emulsion (C/W HIPEs) was developed and stabilized with polyvinyl alcohol (PVA) for the formation of chitosan oligosaccharide/poly(acrylamide-co-sodium 4-styrene sulfonate) [COS/P(AM-co-SSS)] monolithic porous hydrogel. The obtained monolith was characterized via FT-IR and SEM. The SEM patterns depicted that the monoliths were interconnected, the void sizes were 78.5 µm, and the interconnected pore throats were 28 μm approximately. Mechanical measurement results indicated that the maximum compress stress of the monolith could reach 334.4 kPa at 90% strain, and it exhibited good mechanical stability. After 200 cycles of compression, it could still recover its original shape without cracking. The obtained COS-based monolith was selected to remove tetracycline (TC) for evaluating the adsorptive features of the interpenetrating pore-containing monolith. The monolithic COS/P(AM-co-SSS) hydrogel behaved with strong antibiotic adsorption capacity (1600.4 mg/g for TC). The adsorption process agreed well with the pseudo-second-order kinetic and Langmuir isothermal models. In addition, the porous monolith had a strong electrostatic force on TC according to the thermodynamic study. This work provides a green route for the development of novel monolithic hydrogels and highlights its potential application in the treatment of antibiotic-containing wastewater.
在此,开发了一种绿色的水包二氧化碳高内相乳液(C/W HIPEs),并用聚乙烯醇(PVA)进行稳定化处理,以形成壳寡糖/聚(丙烯酰胺 - 共 - 4 - 苯乙烯磺酸钠)[COS/P(AM - co - SSS)]整体式多孔水凝胶。通过傅里叶变换红外光谱(FT - IR)和扫描电子显微镜(SEM)对所得整体材料进行了表征。SEM图像显示,整体材料相互连通,孔隙尺寸为78.5 µm,相互连通的孔喉约为28 µm。力学测量结果表明,整体材料在90%应变下的最大压缩应力可达334.4 kPa,并且表现出良好的力学稳定性。经过200次压缩循环后,它仍能恢复其原始形状而不破裂。选择所得的基于COS的整体材料去除四环素(TC),以评估含互穿孔隙的整体材料的吸附特性。整体式COS/P(AM - co - SSS)水凝胶表现出很强的抗生素吸附能力(对TC的吸附量为1600.4 mg/g)。吸附过程与准二级动力学和朗缪尔等温模型吻合良好。此外,根据热力学研究,多孔整体材料对TC具有很强的静电力。这项工作为新型整体式水凝胶的开发提供了一条绿色途径,并突出了其在处理含抗生素废水方面的潜在应用。