State-of-the-Art Materials for Adsorptive Heat Energy Conversion

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Abstract

The chapter is focused on state of the art of materials for adsorptive heat energy conversion basic principles for substantiation of working pair choice. Types of heat storage materials based on heat storage mechanism were compared. Sensible heat mechanism of thermal energy is based on increasing the temperature of the material. Phase-change mechanism of heat energy storage concerns with alternating reversible processes of phase-changing. As a rule, they are mainly melting-crystallization. Thermo-chemical heat energy storage mechanism is based on reversible chemical reactions. Limitations of conventional sensible heat storage are shown to lowest density of heat energy storage determined by sensible heat of materials, which led to large mass storage units and additional needs of large areas and building volumes, calculated according to heat storage density, constant changing the temperature when discharged, the need for a large overheating of heat storage media. The main defects of phase-change materials are instability of properties of heat-accumulating substances in multiple cycles of crystallization – melting, degradation in time, corrosion activity, the need for developed surfaces of heat exchange and environmental danger. Commercilisation of thermal chemical storage materials is strongly limited by high operating temperatures of thermal chemical storage materials, which are unacceptable for systems of district heating and decentralized heat supply due to sanitary regulations, impropriety for multifold cycling because of irreversibility of a wide range of chemical reactions. Perspective of adsorptive heat energy storage and conversion is shown. Interval of operating temperatures and heat storage density of conventional adsorptive materials are shown to be intermediate between phase-change and thermal chemical heat storage materials. Properties of probable adsorptive heat storage materials were analysed according with literary data. Low adsorptive capacity of conventional adsorbents results in low heat of adsorption and heat energy storage density. Salts forming crystalline hydrate occur to exhibit rather high energy storage density of 1.9–2.7 GJ/m3 of crystalline hydrate, but their application is strongly inhibited not only by physical and chemical instability along with the corrosive activity of these salts at high temperatures, but instability in multifold cycling, degradation in time, and an underdeveloped heat exchange surface. As engineering solution, modification of conventional adsorbents with salt can be considered. Composites ‘salt inside porous matrix' is shown to be promising alternative to conventional adsorbents. Main advantages of these materials are low regeneration temperature and high adsorptive capacity. Crucial impediments of industrial introduction of composite adsorbents ‘salt inside porous matrix' is shown to be complex technology of their production based on rather expensive dry and wet impregnation of porous media by crystalline hydrate solutions. As an alternative, sol gel method for obtaining composite adsorbents ‘silica gel – crystalline hydrate' developed by authors is suggested. The adsorption properties of the obtained composite adsorbents ‘silica gel – sodium sulphate' and ‘silica gel – sodium acetate' are shown to be non-linear combinations of characteristics of silica gel and massive salt. The key distinction of kinetics of adsorption of water vapor with massive salts and composites obtained with sol gel method is shown to be difference limitative stage of process. The adsorption of water with massive crystalline hydrates is shown to be complicated by kinetic limitations. For composite adsorbents limiting stage is water transport through the pore system. Composites ‘slilica gel – crystalline hydrate' are shown to be a promising material for adsorptive heat energy storage and conversion.
最先进的吸附热能转换材料
本章重点介绍了吸附热能转换材料的最新研究进展,以及工作对选择的基本原理。根据储热机理对不同类型的储热材料进行了比较。热能的显热机理是建立在提高材料温度的基础上的。热能储存的相变机理涉及交替可逆的相变过程。通常,它们主要是熔融结晶。热化学储热机理是建立在可逆化学反应基础上的。传统的显热蓄热的局限性表现在最低的热能储存密度由材料的显热决定,这导致了大容量的存储单元和额外的需要大面积和建筑体积,根据蓄热密度计算,排放时不断改变温度,需要较大的过热蓄热介质。相变材料的主要缺陷是:积热物质在结晶-熔化多循环过程中性能不稳定、及时降解、腐蚀活性强、需要发达的换热面和环境危险性大。热化学储存材料的商业化受到热化学储存材料的高工作温度的强烈限制,由于卫生法规,这对于区域供热和分散供热系统是不可接受的,由于大范围化学反应的不可逆性,多次循环是不合适的。展望了吸附式热能储存与转化的前景。传统吸附材料的工作温度间隔和蓄热密度介于相变和热化学储热材料之间。根据文献资料分析了可能的吸附性储热材料的性能。传统吸附剂的吸附能力较低,导致吸附热和蓄热密度较低。形成结晶水合物的盐具有较高的储能密度(1.9 ~ 2.7 GJ/m3),但由于盐在高温下的物理化学不稳定性和腐蚀性,以及多次循环的不稳定性、及时降解的不稳定性和不发达的换热表面,极大地抑制了它们的应用。作为工程解决方案,可以考虑用盐对常规吸附剂进行改性。多孔盐基复合材料是传统吸附剂的理想替代品。这些材料的主要优点是再生温度低,吸附能力高。复合吸附剂“多孔基质内盐”的工业引入的关键障碍是其生产技术复杂,其生产工艺基于晶体水合物溶液对多孔介质进行干湿浸渍的相当昂贵的工艺。作为一种替代方法,建议采用溶胶-凝胶法制备复合吸附剂“硅胶-结晶水合物”。所得的“硅胶-硫酸钠”和“硅胶-乙酸钠”复合吸附剂的吸附性能是硅胶和块状盐特性的非线性组合。用溶胶-凝胶法获得的大质量盐和复合材料吸附水蒸气动力学的关键区别在于过程的不同限制阶段。大量结晶水合物对水的吸附由于动力学限制而变得复杂。对于复合吸附剂,限制阶段是水通过孔隙系统的输送。“硅凝胶-结晶水合物”复合材料是一种很有前途的吸附式热能储存和转化材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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