化学工程
蒸发
自愈水凝胶
材料科学
海水
石墨烯
氧化物
多孔性
纳米技术
复合材料
高分子化学
物理
地质学
工程类
冶金
海洋学
热力学
作者
Chen Yang,Hongsen Qiu,Xianfeng Li,Qikun Tong,Martin Jensen,Qing Li,Ning Wang
标识
DOI:10.1016/j.apsusc.2022.152483
摘要
Three-Level pore structure with ultrahigh transport enhances the salt-resistant, antifouling performance and reduces the water evaporation enthalpy and increases the water evaporation rate of the hydrogel. • Three-level pore structure hydrogels (TLPSHs) were prepared by PVA and rGO. • The micro-environment was proposed to explain the decrease of evaporation enthalpy. • The TLPSHs with 88 % porosity has more than 97 % sunlight absorption. • The TLPSHs shown a stable evaporation rate of 1.65 kg m -2 h −1 . Photothermal evaporation materials have drawn attention owing to their high solar energy utilization. In this work, a series of three-level pore structure hydrogels (TLPSHs) consisting of polyvinyl alcohol (PVA), graphene oxide (GO) or reduced graphene oxide (rGO) are prepared. The hydrogel with PVA crosslinked with rGO shows the most promising properties mainly owing to its three-level pore structure being a combination of nanosized pores for low enthalpy water evaporation and a broad distribution of micronsized pores facilitating water transport into said nanosized pores. When varying the content of rGO/PVA between 5 and 15 wt%, the 10 wt% loading gives the highest water evaporation rate and energy conversion efficient owing to its microstructure combining intra water hydrogen disruption and water transport. The TLPSHs with 88 % porosity has more than 97 % sunlight absorption throughout the UV–Vis-NIR spectrum and stable evaporation rate (1.65 kg m -2 h −1 ) under 1 sun irradiation. The hydrogel rejects salt by having a higher temperature than the surrounding seawater which causes salt to precipitate in the water rather than on the hydrogel evaporator when the saturation limit is reached. Lastly, the scalability and real life applicability is demonstrated through outdoor experiments on seawater.
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