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Desalination via formation of binary clathrate hydrates.

机译:通过形成二元笼形水合物进行脱盐。

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摘要

Desalination through formation of single-component hydrates, actively pursued in the 1970s, suffers from fact that these hydrates usually require low temperatures and/or high pressures to form. This dissertation focuses on binary clathrate hydrates, where the larger hydrate former occupies the larger cavities of a sII-type hydrate and the smaller helper gas occupies the smaller cavities. Binary hydrates, which can be formed at higher temperatures and/or lower pressures than single-component hydrates, could potentially lower the cost of hydrate-based desalination.;In this dissertation, the thermodynamics and kinetics of formation of cyclopentane-methane and cyclopentane-carbon dioxide hydrates in fresh water and brine solutions are studied experimentally. Hydrate formation experiments were conducted in a stirred tank in the 280-295K and 1-3 MPa range and at different stirring rates. From the temporal evolution of pressure and temperature, the hydrate formation rate and the fractional occupancy of the small cavity by the helper gas were extracted. In freshwater, the hydrate growth rate mainly depends on the degree of subcooling and the extent of hydrate formation, with the mass transfer of the helper gas being an important rate-controlling factor. Salt is found to affect the binary hydrate formation process in two ways. First, it shifts the hydrate equilibrium curves so it takes a higher pressure (at the same temperature) to achieve the same degree of subcooling. Second, the concentration polarization associated with rejection of salt by the growing hydrates particles imposes a moderate mass transfer resistance on the hydrate formation process. Nevertheless, the binary hydrate growth rate in brine solutions is found to be comparable to that in fresh water under the same subcooling level.;Poor mixing was found to be an issue during the formation of cyclopentane-carbon dioxide hydrates, but not in the case of cyclopentane-methane hydrates. Nevertheless, the hydrate formation rates for both systems were found to be comparable. A new displacement washing procedure to separate the hydrate crystals from brine has been developed and experimentally tested, demonstrating good hydrate recovery ratio and washing efficiency.
机译:在1970年代积极进行的通过形成单组分水合物进行脱盐的事实是,这些水合物通常需要低温和/或高压才能形成。本文主要研究二元包合物水合物,其中较大的水合物前体占据sII型水合物的较大腔体,较小的辅助气体占据较小的腔体。与单组分水合物相比,二元水合物可以在更高的温度和/或更低的压力下形成,可以潜在地降低基于水合物的脱盐的成本。实验研究了淡水和盐水溶液中的二氧化碳水合物。在280-295K和1-3 MPa范围内的搅拌釜中以不同的搅拌速率进行水合物形成实验。从压力和温度的时间演化过程中,提取出水合物的形成速率和辅助气体在小腔中的占比。在淡水中,水合物的生长速率主要取决于过冷程度和水合物形成的程度,辅助气体的传质是重要的速率控制因素。发现盐以两种方式影响二元水合物的形成过程。首先,它会移动水合物平衡曲线,因此需要较高的压力(在相同的温度下)才能达到相同的过冷度。第二,与增长的水合物颗粒排斥盐分有关的浓度极化对水合物形成过程施加了适度的传质阻力。然而,在相同的过冷度下,盐水溶液中的二元水合物增长率仍可与淡水相当。在环戊烷-二氧化碳水合物的形成过程中发现混合不良是一个问题,但情况并非如此环戊烷甲烷水合物。然而,发现两个系统的水合物形成速率是可比较的。已经开发出了一种新的置换洗涤程序,用于从盐水中分离出水合物晶体,并进行了实验测试,证明了良好的水合物回收率和洗涤效率。

著录项

  • 作者

    Cai, Lichao.;

  • 作者单位

    Princeton University.;

  • 授予单位 Princeton University.;
  • 学科 Chemical engineering.
  • 学位 Ph.D.
  • 年度 2016
  • 页码 147 p.
  • 总页数 147
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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