Song Tianyi, Zhang Jinhai, Li Wei, Ma Jie, Hu Shen, Liu Jianxiu, Li Xiaonan, Hu Wenfeng, Lan Chunming, Tian Guohua, Jin Tingxiang, Han Yuexin, Wang Jiancheng, Gong Junjie, Cheng Chuanxiao
School of Energy and Power Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002, China.
Longhua Technology Group (Luoyang) Co., Ltd., LuoYang 471026, China.
ACS Omega. 2023 Oct 25;8(44):41232-41242. doi: 10.1021/acsomega.3c04578. eCollection 2023 Nov 7.
Rapid formation of the CO hydrate can be significantly induced by the gaseous thermodynamic promoter 1,1,1,2-tetrafluoroethane(R134a) due to the mild phase equilibrium conditions, although the formation mechanism and dynamic behavior are not clear. Therefore, a visual experimental system was developed to study the effects of different concentrations of R134a on the induction time, gas consumption, and growth morphology of the CO hydrate. At the same time, the combined effects under stirring and sodium dodecyl sulfate (SDS) systems were also studied. In addition, visualization and experimental model diagrams were combined to explain the fast formation mechanism of the R134a/CO hydrate. The results show that the CO hydrate average conversion rate was increased by more than 63% with the addition of mixed trace R134a(7%). A special phenomenon is found that two temperature peaks appear on the hydrate formation temperature curve, corresponding to two different stages of hydrate formation when stirring or SDS is added to the mixed gas reaction system. Furthermore, the gas consumption in stirring and SDS systems increases by 9 and 44%, respectively. Finally, it is also found that the R134a/CO mixed hydrate formed under the action of SDS has a "capillary" mechanism, which provides a gas-liquid phase exchange channel and a large number of nucleation sites for CO hydrate, thus promoting the formation of CO hydrate. This paper provides a novel, simple, and efficient method for CO hydrate gas storage technology.
气态热力学促进剂1,1,1,2-四氟乙烷(R134a)可通过温和的相平衡条件显著诱导CO水合物的快速形成,尽管其形成机理和动力学行为尚不清楚。因此,开发了一种可视化实验系统,以研究不同浓度的R134a对CO水合物诱导时间、气体消耗和生长形态的影响。同时,还研究了搅拌和十二烷基硫酸钠(SDS)体系下的联合作用。此外,结合可视化和实验模型图来解释R134a/CO水合物的快速形成机理。结果表明,添加混合微量R134a(7%)时,CO水合物的平均转化率提高了63%以上。发现一个特殊现象,即水合物形成温度曲线上出现两个温度峰值,分别对应于在混合气体反应体系中添加搅拌或SDS时水合物形成的两个不同阶段。此外,搅拌和SDS体系中的气体消耗分别增加了9%和44%。最后,还发现SDS作用下形成的R134a/CO混合水合物具有“毛细管”机制,为CO水合物提供了气液相交换通道和大量成核位点,从而促进了CO水合物的形成。本文为CO水合物储气技术提供了一种新颖、简单且高效的方法。