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Enhanced clathrate hydrate formation kinetics at near ambient temperatures and moderate pressures: Application to natural gas storage

机译:在接近环境温度和中等压力下增强包合物水合物形成动力学:在天然气存储中的应用

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SNG (solidified natural gas) technology via clathrate hydrates is a potential method for large scale stationary storage of natural gas. Clathrate hydrate formation kinetics in presence of methane and 5.6 mol% tetrahydrofuran (THF) was investigated in an unstirred reactor configuration at moderate pressure and temperature conditions. It is well known that the presence of THF generally improves the thermodynamic stability of the resulting hydrate. In order to study the scale-up potential of this approach, kinetics of hydrate growth at temperatures close to ambient conditions and moderate pressures is required. Hydrate formation experiments were performed at three different temperatures - 283.2 K, 288.2 K and 293.2 K and at experimental pressures of 7.2 MPa, 5.0 and 3.0 MPa. Further, we report a synergistic effect of kinetic promotion of mixed methane hydrate formation by coupling THF and sodium dodecyl sulfate (SDS) at 293.2 K. For the first time, we observe rapid mixed methane/THF hydrate formation kinetics at 293.2 K in presence of just 100 ppm sodium dodecyl sulfate surfactant with methane gas uptake of 3.45 (+/- 0.17) kmol/m(3) of water in 1 h. This is also the first study to demonstrate such rapid hydrate formation kinetics with significant methane storage capacity at temperature of 293.2 K (closer to the ambient temperature). Further, substantial methane gas uptake of 3.52 (+/- 0.13) kmol/m(3) of water is possible even at reduced experimental pressure of 3.0 MPa and 283.2 K in 2 h. Minimal energy requirement in an unstirred reactor for mixed methane/THF hydrate formation storage can propel the SNG technology for large scale commercial deployment. Further improvement in the process can be achieved by optimizing the cooling requirement through innovative reactor design and operating the process in a semi-batch or continuous mode. (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过包合物水合物的SNG(固态天然气)技术是大规模固定存储天然气的一种潜在方法。在温和的压力和温度条件下,在无搅拌的反应器配置中研究了在甲烷和5.6 mol%四氢呋喃(THF)存在下的笼形水合物形成动力学。众所周知,THF的存在通常会改善所得水合物的热力学稳定性。为了研究这种方法的放大潜力,需要在接近环境条件和中等压力的温度下水合物生长的动力学。在三个不同的温度-283.2 K,288.2 K和293.2 K以及7.2 MPa,5.0和3.0 MPa的实验压力下进行水合物形成实验。此外,我们报告了通过在293.2 K下偶合THF和十二烷基硫酸钠(SDS)动力学促进混合甲烷水合物形成动力学的协同效应。首次,我们观察到在293.2 K存在下快速的甲烷/ THF水合物混合动力学形成动力学。仅仅100 ppm的十二烷基硫酸钠表面活性剂,在1小时内甲烷气体吸收3.45(+/- 0.17)kmol / m(3)的水。这也是第一个证明在293.2 K(更接近环境温度)的温度下具有显着甲烷存储能力的快速水合物形成动力学的研究。此外,即使在2个小时内降低了3.0 MPa和283.2 K的实验压力下,仍可能吸收3.52(+/- 0.13)kmol / m(3)水的大量甲烷气体。在非搅拌反应器中用于混合甲烷/ THF水合物形成物存储的最小能量需求可以推动SNG技术用于大规模商业部署。通过创新的反应器设计优化冷却要求,并以半间歇或连续模式运行过程,可以进一步改善过程。 (C)2016 Elsevier Ltd.保留所有权利。

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