Sustainable hydrate inhibition: Pectin and MEG synergy for deep-sea environments

IF 4.2 3区 工程技术 Q2 ENERGY & FUELS
Ankur Singh , Shanker Krishna , Ajay Suri , Lavish Kumar Singh , Isaac Wilson
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Abstract

To ensure the continuous operation of the oil and gas industry, it is imperative to maintain an uninterrupted flow of oil and gas through pipelines and pay specific attention to preventing disruptions caused by hydrate blockages. Kinetic hydrate inhibitors (KHIs) have garnered considerable interest due to their capacity for effective hydrate prevention with minimal dosages typically ranging from 0.5 wt% to 2 wt%, guaranteeing both safety and efficiency. While some KHIs, such as amino acids and certain classes of ionic liquids, are known to be biodegradable, it is crucial to explore, develop, and thoroughly evaluate more natural and sustainable alternatives to these KHIs. This study investigated the potential of pectin as a biodegradable HI and examines its performance in synergism with monoethylene glycol (MEG). To assess its inhibitory performance, we conducted measurements of the induction time (IT) and hydrate nucleation temperature (T0) essential for hydrate formation under different conditions. The experimental outcomes indicated that pectin demonstrated slightly lower performance in comparison with commercial KHIs. However, its performance improved significantly when combined with a concentration of MEG. A blend of 0.25 wt% pectin and 2 wt% MEG offered an IT of 6.53 h, while poly(vinyl pyrrolidone) (PVP) and poly(vinyl caprolactam) (PVCap) at 0.25 wt% provided ITs of 4.9 h and 5.9 h, respectively. IT escalated from 2.13 h at 0 wt% MEG to 7.99 h at a MEG concentration of 5 wt%, while T0 exhibited a notable decrease from 8.32 °C at 0 wt% MEG to 1.39 °C at 5 wt% MEG. The identified synergy between pectin and MEG in hydrate inhibition suggests substantial potential for advancing deep-sea hydrate risk management strategies in future research.
可持续水合物抑制:果胶和MEG在深海环境中的协同作用
为了确保油气行业的持续运行,必须保持油气通过管道的不间断流动,并特别注意防止水合物堵塞造成的中断。动能水合物抑制剂(KHIs)因其具有有效防止水合物的能力而获得了相当大的兴趣,其最小剂量通常为0.5 wt%至2 wt%,保证了安全性和有效性。虽然已知一些khi,如氨基酸和某些类型的离子液体是可生物降解的,但探索、开发和彻底评估这些khi的更天然和可持续的替代品至关重要。本研究探讨了果胶作为可生物降解HI的潜力,并考察了其与单乙二醇(MEG)协同作用的性能。为了评估其抑制性能,我们测量了不同条件下水合物形成所需的诱导时间(IT)和水合物成核温度(T0)。实验结果表明,与商业KHIs相比,果胶的性能略低。然而,当与MEG浓度结合使用时,其性能显著提高。0.25 wt%的果胶和2 wt%的MEG的混合物提供了6.53 h的ITs,而聚乙烯醇吡啶酮(PVP)和聚乙烯醇己内酰胺(PVCap)在0.25 wt%的ITs分别为4.9 h和5.9 h。当MEG浓度为5 wt%时,IT从0 wt%时的2.13 h上升到7.99 h,而T0则从0 wt% MEG时的8.32°C显著下降到5 wt% MEG时的1.39°C。果胶和MEG在水合物抑制中的协同作用表明,在未来的研究中,推进深海水合物风险管理策略具有巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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