Deep learning-assisted phase equilibrium analysis for producing natural hydrogen

被引:33
作者
Zhang, Tao [1 ]
Zhang, Yanhui [1 ]
Katterbauer, Klemens [2 ]
Al Shehri, Abdallah [2 ]
Sun, Shuyu [1 ]
Hoteit, Ibrahim [1 ]
机构
[1] King Abdullah Univ Sci & Technol, Thuwal, Saudi Arabia
[2] Saudi Aramco, Dhahran, Saudi Arabia
关键词
White hydrogen; Phase equilibrium; Flash calculation; Thermodynamics -informed neural; network; EQUATION-OF-STATE; HYDRATE; PROPANE; VOLUME; CAPILLARITY; TEMPERATURE; MIXTURES; DIOXIDE; MOLES;
D O I
10.1016/j.ijhydene.2023.09.097
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of natural hydrogen is an emerging topic in the current energy transition trend. The production process involves compositional multiphase flow via subsurface porous media. This makes studying the compositional phase equilibrium behavior essential for reliable reservoir simulation and prediction. Herein, we develop an iterative flash calculation scheme and a deep learning algorithm using a thermodynamics-informed neural network (TINN) to perform accurate, robust, and fast phase equilibrium calculations for realistic fluid mixtures of natural hydrogen. The application of TINN architecture can accelerate the calculations for nearly 20 times. The effect of capillarity on phase equilibrium states is demonstrated. Based on simulation results, suggestions for the natural hydrogen industry chain are provided to control the possible phase transitions under certain environmental conditions that may be observed in the natural hydrogen reservoirs, storage and transportation facilities. The extremely low critical temperature of hydrogen challenges the robustness of flash calculations but facilitates the separation of impurities by liquefying certain undesired species. Moreover, phase transitions under control can be an effective approach for carbon dioxide capture and sequestration with optimized operating conditions over the phase equilibrium analysis. (c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:473 / 486
页数:14
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