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Eco-friendly synthesis of chemically cross-linked chitosan/cellulose nanocrystal/CMK-3 aerogel based shape-stable phase change material with enhanced energy conversion and storage

纤维素 材料科学 纳米晶 壳聚糖 气凝胶 相变 环境友好型 化学工程 相变材料 相(物质) 储能 纳米技术 化学 有机化学 工程物理 工程类 物理 功率(物理) 生物 量子力学 生态学
作者
Miao Cheng,Yifan Yuan,Huaijia Jing,Jing Hu,Qianqian Liu,Tao Wei,Ruirui Wang,Wanfei Li,Бо Лю
出处
期刊:Carbohydrate Polymers [Elsevier BV]
卷期号:324: 121514-121514 被引量:30
标识
DOI:10.1016/j.carbpol.2023.121514
摘要

Phase change materials (PCMs) have attracted numerous attention owing to their high energy storage density, cost-effective and operationally simple, however, the "solid-liquid" leakage and limited solar absorbance seriously hinder their widespread applications. Herein, an innovative chitosan/cellulose nanocrystal/CMK-3 (CS/CNC/CMK-3) aerogel based shape-stable PCM (SSPCM) was successfully synthesized, in which chemically cross-linked CS and CNC acted as three-dimensional supporting skeleton, CMK-3 endowed solar-to-thermal energy conversion ability and the impregnating polyethylene glycol (PEG) acted as the latent heat storage unit. The as-synthesized CS/CNC/CMK-3 aerogel/PEG (CCCA/PEG) showed ultrahigh melting/crystallization enthalpy of 178.5/171.1 J g-1 and excellent shape stability. The PEG was effectively embedded into the hierarchical porous architecture and the composite PCM could preserve its original shape without any leakage even compressed above the melting point of PEG. Meanwhile, the CCCA/PEG exhibited robust thermal reliability with an ultralow enthalpy fading rate of 0.030 ± 0.012 % per cycle over 100 thermal cycles. Intriguingly, the introduction of CMK-3 also significantly improved the solar-to-thermal energy conversion performance of CCCA/PEG, and a high solar-to-thermal conversion efficiency of 93.1 % could be realized. This work provided a potential strategy to design and synthesize high-performance sustainable SSPCM, which showed tremendous potential in the practical solar energy harvesting, conversion and storage applications.
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