The synthesis and evaluation of two new gas hydrate kinetic inhibitors

IF 5 3区 工程技术 Q2 ENERGY & FUELS Natural Gas Industry B Pub Date : 2026-04-01 Epub Date: 2026-04-22 DOI:10.1016/j.ngib.2026.03.002
Huang Liu , Minghao Liu , Jianfen Du , Qingping Li , Ping Guo , Yanghui Liu
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Abstract

Gas hydrate plugging is a common yet hazardous problem during oil and gas reservoir exploitation, compelling the petroleum industry to invest substantial resources annually in mitigation strategies. Two novel hydrate kinetic inhibitors (HKIs), a PVP derivative (PVP-DP) and a PVCap derivative (PVCap-DP), were synthesized and systematically evaluated. Structural characterization by FT-IR, NMR, and TG analyses confirmed increased molecular weights and the introduction of additional polar functional groups relative to the present polymers. In pure water at a subcooling temperature of 6.2 K and a concentration (Cp) of 1 wt%, the methane hydrate induction times (Ih) for PVP-DP and PVCap-DP were 358 min and 395 min, respectively. These values significantly exceed those observed in distilled water (23 min) and in systems containing commercial HKIs, such as PVP (138 min) and VC-713 (272 min). Increasing Cp to 3 wt% further prolonged Ih to 911 min and 964 min, respectively. Even at a higher subcooling of 8.4 K, Ih remained considerable at 126 min and 158 min, demonstrating sustained inhibition under more severe thermodynamic driving forces. Synergistic effects were observed when HKIs (3 wt%) were combined with glycol (1 wt%), resulting in Ih values of 230 min and 268 min. Increasing the glycol concentration to 3 wt% maintained a strong inhibition performance, with Ih values of 211 min and 238 min even at a subcooling of 9 K. In addition, both derivatives exhibited effective inhibition in water/diesel emulsion systems. At 6.2 K subcooling, the PVP-DP (3 wt%)–water/diesel emulsion system achieved an Ih of 404 min, which was markedly longer than that of the uninhibited water/diesel emulsion (51 min), although the emulsion phase moderately reduced the inhibitor efficiency. Overall, PVP-DP and PVCap-DP demonstrate strong kinetic inhibition performance against the formation of natural gas hydrate in both aqueous and emulsion systems, indicating promising application potential in complex production environments.
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两种新型天然气水合物动力学抑制剂的合成与评价
天然气水合物堵塞是油气开发过程中常见而又危险的问题,迫使石油工业每年投入大量资源用于缓解策略。合成了PVP衍生物(PVP- dp)和PVCap衍生物(PVCap- dp)两种新型水合物动力学抑制剂(HKIs),并对其进行了系统评价。通过FT-IR, NMR和TG分析的结构表征证实了相对于现有聚合物的分子量增加和引入了额外的极性官能团。在过冷温度为6.2 K、浓度为1 wt%的纯水条件下,PVP-DP和PVCap-DP的甲烷水合物诱导时间分别为358 min和395 min。这些值明显超过在蒸馏水(23分钟)和含有商业HKIs的系统中观察到的值,例如PVP(138分钟)和VC-713(272分钟)。将Cp增加至3 wt%,可使Ih分别延长至911 min和964 min。即使在更高的过冷度8.4 K时,Ih在126 min和158 min时仍然相当可观,在更严重的热力学驱动力下显示出持续的抑制作用。当HKIs (3 wt%)与乙二醇(1 wt%)联合使用时,观察到协同效应,导致Ih值为230 min和268 min。将乙二醇浓度增加到3wt %,保持了较强的缓蚀性能,即使在过冷9 K时,Ih值仍为211 min和238 min。此外,这两种衍生物在水/柴油乳液体系中都表现出有效的抑制作用。在6.2 K过冷时,PVP-DP (3 wt%) -水/柴油乳化液体系的Ih达到404 min,明显高于未抑制的水/柴油乳化液(51 min),尽管乳化液相适度降低了抑制剂的效率。总的来说,PVP-DP和PVCap-DP在水体系和乳液体系中对天然气水合物的形成都有很强的动力学抑制作用,在复杂的生产环境中具有广阔的应用前景。
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来源期刊
Natural Gas Industry B
Natural Gas Industry B Earth and Planetary Sciences-Geology
CiteScore
5.80
自引率
6.10%
发文量
46
审稿时长
79 days
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