Gas hydrate formation probability and growth rate as a function of kinetic hydrate inhibitor (KHI) concentration

被引:59
作者
Lim, Vincent W. S. [1 ]
Metaxas, Peter J. [1 ]
Stanwix, Paul L. [1 ]
Johns, Michael L. [1 ]
Haandrikman, Gert [2 ]
Crosby, Daniel [3 ]
Aman, Zachary M. [1 ]
May, Eric F. [1 ]
机构
[1] Univ Western Australia, Sch Engn, Fluid Sci & Resources, 35 Stirling Highway, Perth, WA 6009, Australia
[2] Shell Global Solut Int BV, POB 3800, NL-1030 BN Amsterdam, Netherlands
[3] Shell Int Explorat & Prod Inc, POB 432,3333 Highway 6 South, Houston, TX 77210 USA
基金
澳大利亚研究理事会;
关键词
Gas hydrates; Formation probability; Subcooling; Kinetic hydrate inhibitors; Growth; CLATHRATE HYDRATE; POLYVINYLPYRROLIDONE PVP; DRIVING-FORCE; METHANE; NUCLEATION; CRYSTALLIZATION;
D O I
10.1016/j.cej.2020.124177
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Kinetic hydrate inhibitors (KHIs) are polymeric based chemicals that delay the nucleation and/or suppress the growth rate of gas hydrate crystals. While KHIs have been used successfully to mitigate hydrate blockage risk during oil and gas production, the mechanisms by which they function remain unclear. In this work, multiple high-pressure stirred automated lag time apparatus (HPS-ALTA) were used to investigate the impact of a KHI on the subcooling formation probability distributions of methane hydrates and the subsequent initial growth rates. Over 3000 hydrate formation events were measured around 12 MPa using seven independent HPS-ALTA cells with KHI concentrations of up to 3 wt% in water. The addition of KHI made hydrate formation much less stochastic: significant reductions occurred in both the width of the formation probability distribution for a given cell, and in the offsets between distributions measured with different cells. Average initial hydrate growth rates were reduced by approximately a factor of 5 as KHI concentration increased, even though the average driving force (subcooling) increased by a factor of up to 3. However, above a KHI concentration of 0.3 wt%, a diminishing return was observed in both the nucleation delay and growth rate suppression. A Classical Nucleation Theory (CNT) framework was applied to investigate whether polymer adsorption onto active nucleation sites could explain the observed delay in formation onset. However, the CNT kinetic parameter extracted from the measured formation probability data increased with concentration, which is opposite to the dependence predicted by the polymer-adsorption model of nucleation suppression by KHIs.
引用
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页数:10
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