碳纳米管
自愈水凝胶
材料科学
蒸发
光热治疗
化学工程
多孔性
聚乙烯醇
纳米技术
焓
脱水
气凝胶
复合材料
化学
工程类
高分子化学
物理
热力学
生物化学
作者
Liming Zhao,Zhengpeng Yang,Jiaojiao Wang,Yun Zhou,Peng Cao,Jian Zhang,Peng Yuan,Yongyi Zhang,Qingwen Li
标识
DOI:10.1016/j.cej.2022.138676
摘要
Photothermal hydrogel, with an inherently modifiable hydrated network, has been widely demonstrated as a promising candidate for efficient water treatment. However, there are still great challenges in architecting abundant interfacial mass transfer channels and avoiding excessive polarity interaction in polymeric hydrogels. Here, a 3D interconnected topological porous hydrogel was proposed to enable cellular carbon nanotube (CNT) structures filled with hydrophilic and thermosensitive nanonetworks via infiltration and crosslinking of polyvinyl alcohol (PVA), polyethyleneimine (PEI) and carbon black particles (CBs). A detailed comparative investigation revealed that hosting with CBs/PVA/PEI polymeric nanonetworks in CNT cellular structures facilitated the interfacial dehydration and the decrease of evaporation enthalpy, confirming that such a novel topological structure leaded to a remarkable increase in hydratable and heatable interfaces. In this regard, the obtained hybrid hydrogel achieved a high water evaporation rate of 3.55 kg m−2h−1 with an efficiency of 92.0 % under 1 sun irradiation, and particularly a superior self-evaporation rate of 0.49 kg m−2h−1 in the dark. More importantly, such hybrid hydrogel demonstrated excellent evaporation performance in weak sunlight and highly humid environments. This work has shed light on new insights to manufacture porous and low-enthalpy photothermal hydrogels for advanced solar-driven water treatment technology.
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