抗团聚剂:水合物结构、气体组成、水合物量和含水效果的研究

Morteza Aminnaji, A. Hase, L. Crombie
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引用次数: 0

摘要

动力学水合物抑制剂(KHIs)和抗团聚剂(AAs)被称为低剂量水合物抑制剂(LDHIs),已广泛用于石油和天然气作业中的天然气水合物预防。与热力学抑制剂(如甲醇和乙二醇)相比,它们具有显著的优势。虽然在KHIs评价方面已经做了大量的工作,但在水合物结构效应、气体成分、含水率和水合物含量方面的评价是AAs的主要目标。为了实验评估不同气体成分(从简单的甲烷系统到多组分天然气系统)中的各种商用原子吸收剂,进行了关井重新启动程序(使用视觉摇摆单元)。利用记录的压力-温度数据,分析了在原子吸收剂存在下水合物生长速率和水合物生成量的动力学。通过压降计算水合物生成量(WCH:水转化为水合物的百分比),建立压力-温度水合物闪蒸。步进加热平衡点测量的实验结果表明,在多组分天然气体系中,形成的水合物不是简单结构的II型水合物,而是按热力学稳定性的顺序形成的多种水合物结构或相。初步的实验研究结果表明,不同气体成分的原子吸收光谱的性能不尽相同。这可能是由于水合物结构对AAs性能的影响。例如,虽然市售的AA(如本文所测试的)不能防止甲烷体系中的水合物聚集/堵塞(体系中形成2%的水合物后发生堵塞),但它在天然气体系中表现出更好的性能。此外,在含AA的富天然气体系(高过冷温度为~ 15℃)中,视觉摇摆池中未观察到水合物堵塞现象,而在相同过冷温度下,贫天然气体系中出现了水合物结块和水合物堵塞现象。推测甲烷水合物结构I可能是导致AAs水合物堵塞失效的主要原因。结果表明,含水百分比、气相组成和AAs浓度对水合物生长速率和水合物堵塞有显著影响。除了增加对AAs现场应用的信心外,研究结果还可能在水合物结构对堵塞和水合物堵塞计算的影响方面具有新的应用前景。为了计算在AAs存在下水合物生长过程中转化为水合物的水的百分比,需要一个强大的压力-温度水合物闪变计算。
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Anti-Agglomerants: Study of Hydrate Structural, Gas Composition, Hydrate Amount, and Water Cut Effect
Kinetic hydrate inhibitors (KHIs) and anti-agglomerants (AAs) – known as low dosage hydrate inhibitors (LDHIs) – have been used widely for gas hydrate prevention in oil and gas operations. They offer significant advantages over thermodynamic inhibitors (e.g., methanol and glycols). While significant works have been done on KHIs evaluation, AAs suffer from their evaluation in terms of hydrate structural effect, gas composition, water cut, and hydrate amount, which are the main objectives of this work. A Shut-in-Restart procedure was carried out to experimentally evaluate (using a visual rocking cell) various commercial AAs in different gas compositions (from a simple methane system to multicomponent natural gas systems). The kinetics of hydrate growth rate and the amount of hydrate formation in the presence of AAs were also analysed using the recorded pressure-temperature data. The amount of hydrate formation (WCH: percentage of water converted to hydrate) was also calculated by pressure drop and establishing the pressure-temperature hydrate flash. The experimental results from the step heating equilibrium point measurement suggest the formation of multiple hydrate structures or phases in order of thermodynamic stability rather than the formation of simple structure II hydrate in the multicomponent natural gas system. The initial findings of experimental studies show that the performance of AAs is not identical for different gas compositions. This is potentially due to the hydrate structural effect on AAs performance. For example, while a commercially available AA (as tested here) could not prevent hydrate agglomeration/blockage in the methane system (plugging occurred after 2% hydrate formed in the system), it showed a much better performance in the natural gas systems. In addition, while hydrate plugging was not observed in the visual rocking cell in the rich natural gas system with AA (at a high subcooling temperature of ∼15°C), some hydrate agglomeration and hydrate plugging were observed for the lean natural gas system at the same subcooling temperature. It is speculated that methane hydrate structure I is potentially the main reason for hydrate plugging and failure of AAs. Finally, the results indicate that water cut%, gas composition, and AAs concentration have a significant effect on hydrate growth rate and hydrate plugging. In addition to increasing confidence in AAs field use, findings potentially have novel applications with respect to hydrate structural effect on plugging and hydrate plug calculation. A robust pressure-temperature hydrate flash calculation is required to calculate the percent of water converted to hydrate during hydrate growth in the presence of AAs.
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