Equilibrium Conditions for Semiclathrate Hydrates Formed with CO2, N2, or CH4 in the Presence of Tri-n-butylphosphine Oxide

被引:27
|
作者
Du, Jianwei [1 ]
Wang, Liguang [1 ]
机构
[1] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
SIMULATED FLUE-GAS; PHASE-EQUILIBRIUM; CARBON-DIOXIDE; DISSOCIATION ENTHALPIES; BROMIDE; METHANE; BUTYL; NITROGEN; SEPARATION; BEHAVIOR;
D O I
10.1021/ie403130h
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
We measured the thermodynamic stability conditions for the N-2, CO2, or CH4 semiclathrate hydrate formed from the aqueous solution of tri-n-butylphosphine oxide (TBPO) at 26 wt %, corresponding to the stoichiometric composition for TBPO center dot 34 center dot 5H(2)O. The measurements were performed in the temperature range 283.71-300.34 K and pressure range 0.35-19.43 MPa with the use of an isochoric equilibrium step-heating pressure-search method. The results showed that the presence of TBPO made these semiclathrate hydrates much more stable than the corresponding pure N-2, CO2, and CH, hydrates. At a given temperature, the semiclathrate hydrate of 26 wt % TB PO solution + CH4 was more stable than that of 26 wt % TBPO solution + CO2, which in turn was more stable than that of 26 wt % TBPO solution + N-2. We analyzed the phase equilibrium data using the Clausius-Clapeyron equation and found that, in the pressure range 0-20 MPa, the mean dissociation enthalpies for the semiclathrate hydrate systems of 26 wt % TBPO solution + N-2, 26 wt % TBPO solution + CO2, and 26 wt % TBPO solution + CH4 were 177.75, 206.23, and 159.00 kJ.mol(-1), respectively.
引用
收藏
页码:1234 / 1241
页数:8
相关论文
共 50 条
  • [1] Phase Equilibria and Dissociation Enthalpies of Tri-n-butylphosphine Oxide Semiclathrate Hydrates Incorporated with CH4, CO2, and H2
    Cha, Jong-Ho
    Kim, Eun Sung
    Lee, Ki Sun
    Kang, Jeong Won
    Kang, Jeong Won
    Kim, Ki-Sub
    JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2013, 58 (12): : 3494 - 3498
  • [2] Phase Equilibria of Double Semiclathrate Hydrates Formed with Tetraamylammonium Bromide Plus CH4, CO2, or N2
    Shi, Lingli
    Liang, Deqing
    JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2015, 60 (09): : 2749 - 2755
  • [3] Phase Equilibrium Conditions for the Double Semiclathrate Hydrate Formed with Tetraamylammonium Chloride Plus CH4, CO2, or N2
    Shi, Ling-Li
    Liang, De-Qing
    JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2014, 59 (11): : 3705 - 3709
  • [4] Equilibrium Conditions for Semiclathrate Hydrates Formed in the CH4 + N2 + O2 + Tetra-n-butyl Ammonium Bromide Systems
    Zhong, Dong-Liang
    Ye, Yang
    Yang, Chen
    JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2011, 56 (06): : 2899 - 2903
  • [5] Phase equilibrium measurements for clathrate hydrates of flue gas (CO2 + N2 + O2) in the presence of tetra-n-butyl ammonium bromide or tri-n-butylphosphine oxide
    Du, Jianwei
    Wang, Liguang
    JOURNAL OF CHEMICAL THERMODYNAMICS, 2015, 88 : 96 - 100
  • [6] Phase equilibrium for ionic semiclathrate hydrate formed with CO2, CH4, or N2 plus tetrabutylphosphonium bromide
    Suginaka, Takuya
    Sakamoto, Hiroki
    Iino, Kento
    Sakakibara, Yusuke
    Ohmura, Ryo
    FLUID PHASE EQUILIBRIA, 2013, 344 : 108 - 111
  • [7] Molecular Simulations of CO2/CH4, CO2/N2 and N2/CH4 Binary Mixed Hydrates
    A. A. Sizova
    S. A. Grintsevich
    M. A. Kochurin
    V. V. Sizov
    E. N. Brodskaya
    Colloid Journal, 2021, 83 : 372 - 378
  • [8] Molecular Simulations of CO2/CH4, CO2/N2 and N2/CH4 Binary Mixed Hydrates
    Sizova, A. A.
    Grintsevich, S. A.
    Kochurin, M. A.
    Sizov, V. V.
    Brodskaya, E. N.
    COLLOID JOURNAL, 2021, 83 (03) : 372 - 378
  • [9] Phase equilibria prediction model for semiclathrate hydrates formed from CH4, CO2, and N2 in the presence of tetra-n-butyl ammonium bromide
    Zhao, Wei-Long
    Yang, Chen
    Wang, Rui-Rui
    ENERGY SOURCES PART A-RECOVERY UTILIZATION AND ENVIRONMENTAL EFFECTS, 2016, 38 (05) : 621 - 627
  • [10] Phase Equilibrium Conditions of Tetrabutyl Ammonium Nitrate + CO2, N2, or CH4 Semiclathrate Hydrate Systems
    Du, Jian-Wei
    Liang, De-Qing
    Li, Dong-Liang
    Chen, Yu-Feng
    Li, Xin-Jun
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2011, 50 (20) : 11720 - 11723