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用于高效收集大气水的TpPa-1共价有机框架增强两性离子水凝胶

TpPa-1 COFs-Enhanced Zwitterion Hydrogel for Efficient Harvesting of Atmospheric Water.

作者信息

Liu Yueli, Fu Jingchao, Zhu Yuhao, Chen Wen

机构信息

State Key Laboratory of Silicate Materials for Architectures, School of Materials Science and Engineering, Wuhan University of Technology, Wuhan, 430070, P. R. China.

Sanya Science and Education Innovation Park, Wuhan University of Technology, Sanya, 572024, P. R. China.

出版信息

ChemSusChem. 2024 Jun 10;17(11):e202400030. doi: 10.1002/cssc.202400030. Epub 2024 Apr 19.

DOI:10.1002/cssc.202400030
PMID:38536019
Abstract

Zwitterionic hydrogel, serving as carriers for hygroscopic salts, holds significant potential in atmospheric water harvesting. However, their further application is limited by structural collapse in high-concentration salt solution and poor photothermal conversion performance. Herein, the graded pore structure of poly-3-[dimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azaniumyl]propane-1-sulfonate (PDMAPS) zwitterionic hydrogel/TpPa-1 covalent organic frameworks (COFs)/LiCl composite (named as PCL composite hydrogel) is proposed, which leads to the accelerated diffusion effect for water molecules. As a result, the vapor adsorption capacity of the optimal composite hydrogel (PCL-42) reaches 2.88 g g within 12 hours under conditions of 25 °C and 90 % RH. Simultaneously, the maximum temperature of PCL-42 composite could reach 53.9 °C after 9 minutes under a simulated solar intensity of 1.0 kW m, releasing 91 % of the adsorbed water in 3 hours, providing a promising prospect for efficient solar-driven atmospheric water harvesting. One cycle could collect 7.55 g of fresh water under outdoor conditions, and the maximum daily water production may reach 2.71 kg kg. The reason lies in that TpPa-1 COFs lead hydrogel to form a gradient pore structure, which may accelerate the transport of water molecules, increase the loading capacity of LiCl and enhance the photothermal property.

摘要

两性离子水凝胶作为吸湿盐的载体,在大气水收集方面具有巨大潜力。然而,它们的进一步应用受到高浓度盐溶液中结构坍塌和光热转换性能差的限制。在此,提出了聚-3-[二甲基-[2-(2-甲基丙烯酰氧基)乙基]铵基]丙烷-1-磺酸盐(PDMAPS)两性离子水凝胶/TpPa-1共价有机框架(COFs)/LiCl复合材料(命名为PCL复合水凝胶)的分级孔结构,这导致了水分子的加速扩散效应。结果,在25°C和90%RH的条件下,最佳复合水凝胶(PCL-42)的蒸汽吸附容量在12小时内达到2.88 g g。同时,在1.0 kW m的模拟太阳强度下,PCL-42复合材料在9分钟后最高温度可达53.9°C,在3小时内释放91%的吸附水,为高效太阳能驱动的大气水收集提供了广阔前景。一个循环在室外条件下可收集7.55 g淡水,最大日产水量可达2.71 kg kg。原因在于TpPa-1 COFs使水凝胶形成梯度孔结构,这可能加速水分子的传输,增加LiCl的负载量并增强光热性能。

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