Cheng Chuanxiao, Wang Fan, Zhang Jun, Qi Tian, Jin Tingxiang, Zhao Jiafei, Zheng Jili, Li Lingjuan, Li Lun, Yang Penglin, Lv Shuai
School of Energy and Power Engineering, Zhengzhou University of Light Industry, Zhengzhou 450002, China.
Key Laboratory of Ocean Energy Utilization and Energy Conservation of Ministry of Education, Dalian University of Technology, Dalian 116024, China.
ACS Omega. 2019 Jul 1;4(7):11397-11407. doi: 10.1021/acsomega.9b01187. eCollection 2019 Jul 31.
Cold storage using hydrates for cooling is a high-efficiency technology. However, this technology suffers from problems such as the stochastic nature of hydrate nucleation, cyclic hydrate formation instability, and a low cold discharge rate. To solve these problems, it is necessary to further clarify the characteristics of hydrate formation and dissociation in different systems. First, a comparative experimental study in pure water and sodium dodecyl sulfate (SDS) solution systems was conducted to explore the influence of SDS on the morphology of the hydrate and the time needed for its formation under visualization conditions. Subsequently, the cyclic hydrate formation stability was investigated at different test temperatures with two types of SDS solution systems-with or without a porous medium. The induction time, full time, and energy consumption time ratio of the first hydrate formation process and the cyclic hydrate reformation process were analyzed. Finally, thermal stimulation combined with depressurization was used to intensify hydrate dissociation compared with single thermal stimulation. The results showed that the growth morphology of hydrate and the time required for its formation in the SDS solution system were obviously different than those in pure water. In addition, the calculation and comparison results revealed that the induction time and full time of cyclic hydrate reformation were shorter and the energy consumption time ratio was smaller in the porous medium. The results indicated that a porous medium could improve the cyclic hydrate formation process by making it more stable and by decreasing time and energy costs. Thermal stimulation combined with depressurization at different backpressures (0.1, 0.2, 0.3, and 0.4 MPa) effectively promoted the decomposition of hydrates, and with the decrease in backpressure, the dissociation time decreased gradually. At a backpressure of 0.1 MPa, the dissociation time was reduced by 150 min. The experimental results presented the formation and dissociation characteristics of 1,1,1,2-tetrafluoroethane hydrates in different systems, which could accelerate the application of gas hydrates in cold storage.
利用水合物进行冷藏是一种高效技术。然而,该技术存在诸如水合物成核的随机性、循环水合物形成的不稳定性以及冷排放率低等问题。为了解决这些问题,有必要进一步阐明不同系统中水合物形成和解离的特性。首先,在纯水和十二烷基硫酸钠(SDS)溶液系统中进行了对比实验研究,以探讨SDS在可视化条件下对水合物形态及其形成所需时间的影响。随后,在不同测试温度下,使用两种类型的SDS溶液系统(有或没有多孔介质)研究了循环水合物形成的稳定性。分析了首次水合物形成过程和循环水合物再形成过程的诱导时间、完全形成时间和能耗时间比。最后,与单一热刺激相比,采用热刺激与减压相结合的方式强化水合物解离。结果表明,SDS溶液系统中水合物的生长形态及其形成所需时间与纯水中明显不同。此外,计算和比较结果表明,在多孔介质中,循环水合物再形成的诱导时间和完全形成时间较短,能耗时间比更小。结果表明,多孔介质可以通过使循环水合物形成过程更稳定、减少时间和能源成本来改善该过程。在不同背压(0.1、0.2、0.3和0.4MPa)下,热刺激与减压相结合有效地促进了水合物的分解,并且随着背压的降低,解离时间逐渐减少。在背压为0.1MPa时,解离时间减少了150分钟。实验结果展示了1,1,1,2 - 四氟乙烷水合物在不同系统中的形成和解离特性,这可以加速气体水合物在冷藏中的应用。