Hydrophobized particles can accelerate nucleation of clathrate hydrates

被引:71
作者
Li, Huijuan [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
Hydrophobicity; Surfactant coating; Induction time; Probability distribution; Nucleation rate; NATURAL-GAS; CARBON-DIOXIDE; METHANE; WATER; KINETICS; GROWTH; HYDROGEN; DRY;
D O I
10.1016/j.fuel.2014.10.005
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
This paper reports the effects of glass particles coated by N,N-dimethyl-N-octadecyl-3-aminopropyl tri-methoxysilyl chloride (DMOAP) and octadecyltrichlorosilane (OTS) on the nucleation of tetrahydrofuran (THF), cyclopentane (CP), tetra-n-butyl ammonium bromide (TBAB) and methane (CH4) hydrates under static conditions with no agitation. Induction-time data were collected and statistically processed in the form of probability (P) distribution of samples undergoing no formation of clathrate hydrates as a function of time. Nucleation rate was calculated by fitting the P values to an equation based on the classical nucleation theory. It was found that within 12 h, the nucleation rates of all four hydrates were significantly increased by introducing OTS-coated (hydrophobic) surfaces. In contrast, DMOAP-coated (partly hydrophobic) glass surfaces and clean (hydrophilic) glass surfaces had no effect on the formation of CP and CH4 hydrates but showed relatively weak promotion effect on the formation of THF and TBAB hydrates. It was also found that the position where OTS-coated particles were loaded was of paramount importance for the nucleation of the hydrates with water-immiscible CP and CH4, and the appropriate loading position was at the guest/water interface. These results suggest that foreign particles when properly hydrophobized and loaded can accelerate clathrate hydrate nucleation. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:440 / 445
页数:6
相关论文
共 38 条
[1]   Interfacial mechanisms governing cyclopentane clathrate hydrate adhesion/cohesion [J].
Aman, Zachary M. ;
Brown, Erika P. ;
Sloan, E. Dendy ;
Sum, Amadeu K. ;
Koh, Carolyn A. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (44) :19796-19806
[2]   Equilibrium data of hydrogen, methane, nitrogen, carbon dioxide, and natural gas in semi-clathrate hydrates of tetrabutyl ammonium bromide [J].
Arjmandi, Mosayyeb ;
Chapoy, Antonin ;
Tohidi, Bahman .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2007, 52 (06) :2153-2158
[3]   Chemical physics: How to keep dry in water [J].
Ball, P .
NATURE, 2003, 423 (6935) :25-26
[4]   Formation of natural gas hydrates in marine sediments 1. Conceptual model of gas hydrate growth conditioned by host sediment properties [J].
Ben Clennell, M ;
Hovland, M ;
Booth, JS ;
Henry, P ;
Winters, WJ .
JOURNAL OF GEOPHYSICAL RESEARCH-SOLID EARTH, 1999, 104 (B10) :22985-23003
[5]  
BLOKZIJL W, 1993, ANGEW CHEM INT EDIT, V32, P1545, DOI 10.1002/anie.199315451
[6]   Gas Storage in "Dry Water" and "Dry Gel" Clathrates [J].
Carter, Benjamin O. ;
Wang, Weixing ;
Adams, Dave. J. ;
Cooper, Andrew I. .
LANGMUIR, 2010, 26 (05) :3186-3193
[7]   SURFACE VIBRATIONAL SPECTROSCOPIC STUDIES OF HYDROGEN-BONDING AND HYDROPHOBICITY [J].
DU, Q ;
FREYSZ, E ;
SHEN, YR .
SCIENCE, 1994, 264 (5160) :826-828
[8]   Effect of membrane surface roughness on colloid-membrane DLVO interactions [J].
Hoek, EMV ;
Bhattacharjee, S ;
Elimelech, M .
LANGMUIR, 2003, 19 (11) :4836-4847
[9]   Study of the structure of a water molecular assembly in a hydrophobic nanospace at low temperature with in situ X-ray diffraction [J].
Iiyama, T ;
Nishikawa, K ;
Suzuki, T ;
Kaneko, K .
CHEMICAL PHYSICS LETTERS, 1997, 274 (1-3) :152-158
[10]   ORIENTATION OF LIQUID-CRYSTALS BY SURFACE COUPLING AGENTS [J].
KAHN, FJ .
APPLIED PHYSICS LETTERS, 1973, 22 (08) :386-388