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Inhibition-Promotion: Dual Effects of Polyvinylpyrrolidone (PVP) on Structure-II Hydrate Nucleation

机译:抑制促进:聚乙烯吡咯烷酮(PVP)对结构II水合物成核的双重影响

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摘要

Polyvinylpyrrolidone (PVP) is known as a kinetic hydrate inhibitor (KHI) and its inhibiting effect on hydrate nucleation and growth has been widely studied and acknowledged. In this work, the effect of PVP on methane-propane hydrate nucleation was examined in high-pressure autoclave at isothermal conditions. We examined PVP at ultralow concentrations of SO and 100 ppm to avoid overlapping effects on nucleation and growth and maintain focus on the nucleation stage of the process. Two experimental pressures (P-exp = 6.1 or 9.0 MPa), two cooling rates (2 K/h or 6 K/h), and six subcooling levels (Delta T) ranging from 6.37-10.05 K were applied to induce nucleation. The induction time for hydrate nucleation increased with PVP present at ultralow concentrations, but intriguingly, PVP demonstrated dual effects of inhibition and promotion on hydrate nucleation rate at the experimental pressures examined. The switch from promoting to inhibiting effect on nucleation rate was seemingly not affected by pressure or cooling rate, but rather dependent on the degree of subcooling, Delta T. As compared to systems without inhibitor, PVP reduced the stationary nucleation rate at Delta T > 9 K. At subcooling levels between 6-9 K, PVP tended to promote the process through an increased nucleation rate. This is the first time a promoting effect of PVP alone on hydrate nucleation rate has been experimentally observed and reported. The cause remains unclear. We propose a hypothesis that the docking orientation of PVP polymers relative to the water cages on the surface of hydrate embryos is a function of temperature and applied subcooling level. Subsequently, a switch of the spatial configuration of PVP molecules could either inhibit or promote hydrate nucleation rate. The experimental study gives new insight into KHI working mechanisms. Further investigations are required to improve our understanding of the observed dual effects of PVP on gas hydrate nucleation.
机译:聚乙烯吡咯烷酮(PVP)被称为动力学水合物抑制剂(KHI),其对水合物成核和生长的抑制作用已得到广泛研究和认可。在这项工作中,在等温条件下的高压高压釜中检查了PVP对甲烷-丙烷水合物成核的影响。我们检查了SO和100 ppm超低浓度下的PVP,以避免对成核和生长产生重叠影响,并保持对工艺成核阶段的关注。施加两个实验压力(P-exp = 6.1或9.0 MPa),两个冷却速率(2 K / h或6 K / h)和六个范围在6.37-10.05 K的过冷度(ΔT)以诱导成核。水合物成核的诱导时间随超低浓度PVP的存在而增加,但有趣的是,在所考察的实验压力下,PVP表现出抑制和促进水合物成核速率的双重作用。从成核速率的促进作用到抑制作用的转变似乎不受压力或冷却速率的影响,而是取决于过冷度DeltaT。与没有抑制剂的系统相比,PVP降低了Delta T> 9时的固定成核速率K.在6-9 K之间的过冷度下,PVP倾向于通过增加成核速率来促进该过程。这是首次通过实验观察和报道了单独的PVP对水合物成核速率的促进作用。原因尚不清楚。我们提出一个假设,即PVP聚合物相对于水合物胚表面上的水笼的对接取向是温度和所施加的过冷度的函数。随后,PVP分子空间构型的改变可能会抑制或促进水合物成核速率。实验研究为KHI工作机制提供了新的见解。需要进一步的研究来增进我们对观察到的PVP对气体水合物成核作用的双重影响的理解。

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  • 来源
    《Energy & fuels》 |2016年第9期|7646-7655|共10页
  • 作者单位

    Univ Stavanger, Fac Sci & Technol, Dept Petr Engn, N-4036 Stavanger, Norway;

    Univ Stavanger, Fac Sci & Technol, Dept Petr Engn, N-4036 Stavanger, Norway;

    Univ Stavanger, Fac Sci & Technol, Dept Math & Nat Sci, N-4036 Stavanger, Norway;

    Univ Stavanger, Fac Sci & Technol, Dept Petr Engn, N-4036 Stavanger, Norway|Norwegian Univ Sci & Technol, Fac Engn Sci & Technol, Dept Petr Engn & Appl Geophys, NTNU, N-7491 Trondheim, Norway;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 00:39:59

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