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Evaluation of various types' equations of state for prediction of rate of double gas hydrate formation based on Kashchiev model in flow loop apparatus

机译:基于环流装置中的Kashchiev模型评估各种状态方程以预测双气体水合物生成速率

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This paper compares the effects of using various types of equations of state such as Peng Robinson (PR), Soave Redlich Kwong (SRK), Esmaeilzadeh - Roshanfeker (ER), Patel Teja (PT) and Valderrama-Patel -Teja (VPT) on the rate of hydrate formation based on the Kashchiev model for gaseous mixtures with experimental data points obtained in a mini flow loop apparatus in presence of the kinetic inhibitors (such as modified starch and L-tyrosine) at various pressures (1-4 MPa) and specified temperature (277.15 K). For this purpose, a laboratory mini flow loop apparatus was set up to measure the rate of gas hydrate formation when a hydrate forming mixture is contacted with water in the presence or absence of dissolved inhibitor under suitable temperature and pressure conditions. In each experiment, a water blend saturated with pure gas is circulated up to a required pressure. Pressure is maintained at a constant value during experimental runs by means of the required gas make-up. The total average absolute deviation was found to be 18.7%, 19.8%, 19.2%, 20.2% and 20.7% of the PR, ER, SRK, VPT and PT equations of state for calculating of gas consumption for gaseous mixtures during gas hydrate formation (in the presence and absence of kinetic gas hydrate inhibitor), respectively. Comparison results between the calculated and experimental data points of gas consumption were obtained in a flow loop indicate that the PR and ER equations of state have lower errors than the SRK, VPT and PT equations of state for this model.
机译:本文比较了使用诸如彭·罗宾逊(PR),索夫·雷德利希·K(Soave Redlich Kwong)(SRK),埃斯梅埃扎德(Esmaeilzadeh-Roshanfeker)(ER),帕特尔·特亚(Patel Teja)(PT)和瓦尔德拉玛-帕特尔(Pader-Tetel)-特亚(VPT)等各种状态方程的影响基于Kashchiev模型的气体混合物的水合物形成速率,该气体混合物具有在各种压力(1-4 MPa)和动力学抑制剂(例如改性淀粉和L-酪氨酸)存在下的微型流动回路装置中获得的实验数据点,并且指定温度(277.15 K)。为此目的,建立了实验室微型流动回路设备,以在合适的温度和压力条件下,在有或没有溶解抑制剂的情况下,将水合物形成混合物与水接触时,测量气体水合物形成的速率。在每个实验中,将充满纯净气体的水混合物循环至所需压力。在实验运行期间,通过所需的气体补充将压力保持在恒定值。发现总平均绝对偏差为PR,ER,SRK,VPT和PT状态方程的18.7%,19.8%,19.2%,20.2%和20.7%,用于计算天然气水合物形成过程中气态混合物的耗气量(分别在存在和不存在动力学气体水合物抑制剂的情况下)。在流动环路中获得的耗气量计算值和实验数据点之间的比较结果表明,该模型的PR和ER状态方程比SRK,VPT和PT状态方程具有更低的误差。

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