Xiaoming Wang, Li Li, Yan Lin, Jin Xu, Jiatao Zhao, Xiaoguang Zhang*, Fei Wang* and Xiaolin Wang,
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引用次数: 0
摘要
将多孔介质用作促进甲烷水合物形成的固定床在基于水合物的能源储存方面具有巨大潜力。本研究首次制备并采用了具有一体式结构和超轻重量的石墨烯气凝胶(GA)作为甲烷水合物形成的固定床。特别是全面研究了石墨烯气凝胶的填充率和疏水亲水特性对促进效率的影响。在 84-95% 的范围内,填充率越低,促进效率越高,当填充率为 84% 时,甲烷储存量和表观储存量分别从 114.4 ± 7.6 和 52.4 ± 6.7 V/V 提高到 146.3 ± 6.5 和 91.1 ± 13.0 V/V。低温扫描电子显微镜(Cryo-SEM)显示,水合物形成于 GA 的内孔,但同时也发现了空孔的存在,表明部分反应溶液从 GA 中迁移出来。幸运的是,通过调节 GA 的亲水疏水特性,可以控制水合物生长过程中反应溶液的迁移,从而优化甲烷的储存能力。更重要的是,与传统介质相比,GA 在重力储存能力方面具有卓越的优势,因此在作为超轻固定床用于水合物储能的工业应用方面具有巨大潜力。
Methane Hydrates Formed in a Porous Graphene Aerogel for Energy Storage
The use of porous media as a fixed bed for promoting methane hydrate formation has been endowed with great potential in hydrate-based energy storage. In this work, a graphene aerogel (GA) with a one-piece structure and ultralight weight was prepared and adopted for the first time as a fixed bed for methane hydrate formation. In particular, the effects of the filling ratio and hydrophobic–hydrophilic properties of GA on the promotion efficiency were comprehensively investigated. In the range of 84–95%, a lower filling ratio resulted in higher promotion efficiency, which at 84% increased the methane storage capacity and apparent storage capacity from 114.4 ± 7.6 and 52.4 ± 6.7 V/V to 146.3 ± 6.5 and 91.1 ± 13.0 V/V, respectively. Cryo-scanning electron microscopy (Cryo-SEM) demonstrated that the hydrates formed in the inner pores of GA but also revealed the existence of empty pores, indicating that part of the reaction solution migrated out of the GA. Fortunately, by regulating the hydrophilic–hydrophobic properties of GA, the migration of the reaction solution during hydrate growth could be controlled, and the methane storage capacity could be optimized. More importantly, GA produced excellent advantages in terms of gravimetric storage capacity over traditional media and, therefore, produced great potential in serving as an ultralight fixed bed for the industrial application of hydrate-based energy storage.
期刊介绍:
The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials.
Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.