高级检索

    两性离子共聚物/聚吡咯复合冻胶的光热水蒸发

    Photothermal Water Evaporation of Zwitterionic Copolymer/Polypyrrole Composite Cryogels

    • 摘要: 在海水的界面光热水蒸发过程中,盐结晶会极大降低蒸发器的蒸发效率。为此,使用两性离子单体甲基丙烯酰乙基磺基甜菜碱(SBMA)与亲水性单体丙烯酰胺(AM)进行冷冻共聚,制备了两性离子共聚物冻胶。通过氧化偶联聚合原位负载聚吡咯,构建光热水蒸发器,利用两性离子的抗聚电解质效应提高蒸发器的耐盐性。通过优化冻胶的共聚组成,结合扫描电子显微镜对不同组成冻胶的孔结构进行微观表征,并采用暗蒸发实验测定其等效蒸发焓。结果表明:当入射光强为1 kW/m2(即在一个太阳光强度照射下)时,蒸发器的纯水蒸发速率最高可达2.39 kg/(m2·h);在8 h的海水蒸发实验中未发生盐结晶现象,最高蒸发速率达到2.41 kg/(m2·h),平均蒸发速率为2.23 kg/(m2·h)。收集的水达到了饮用水标准。

       

      Abstract: During the interfacial photothermal water evaporation process of seawater, salt crystallization significantly reduces the evaporation efficiency of the evaporator. To address this challenge, a series of zwitterionic copolymer cryogels were synthesized through cryogenic copolymerization of the zwitterionic monomer, sulfobetaine methacrylate, and the hydrophilic monomer, acrylamide. Subsequently, a photothermal water evaporator was constructed by in-situ loading polypyrrole via oxidative coupling polymerization. The salt resistance of the evaporator was enhanced through the anti-polyelectrolyte effect of the zwitterionic side groups and the water convection between the bulk water and the evaporation surface. To systematically clarify the dependence of equivalent evaporation enthalpy on copolymer composition and pore architecture, we optimized the copolymerization composition of cryogels. Scanning electron microscopy was used to observe the pore structures of cryogels with different compositions. Additionally, dark evaporation experiments were performed to determine their equivalent evaporation enthalpies. Under simulated one-sun illumination (incident intensity: 1 kW/m2), the evaporator achieved a maximum evaporation rate of 2.39 kg/(m2·h) for pure water. In an 8 h seawater evaporation test, no salt crystallization was observed while the evaporator achieved a peak evaporation rate of 2.41 kg/(m2·h) with an average value of 2.23 kg/(m2·h). Notably, the quality of the collected water meets the drinking water standards.

       

    /

    返回文章
    返回