Clathrate Hydrate Formation: Dependence on Aqueous Hydration Number

被引:21
作者
Dec, Steven F. [1 ]
机构
[1] Colorado Sch Mines, Dept Chem & Geochem, Golden, CO 80401 USA
关键词
METHANE HYDRATE; GAS HYDRATE; ICE SURFACES; LIQUID WATER; XE-129; NMR; ETHANE; NUCLEATION; SIMULATIONS; SOLUBILITY; PRESSURE;
D O I
10.1021/jp9009977
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The formation of methane-ethane (C1-C2) clathrate hydrate was studied with high-resolution, solid-state (13)C NMR and density functional theory techniques. The (13)C NMR experiments yield a number of significant findings: (1) the hydration number of C2(aq) is 26, (2) the initial quantity of C2-5(12)6(2) sI hydrate cages outnumber C1-5(12) cages at 274 K, (3) C1-C2 sII hydrate forms at a C1-C2 gas phase composition where only sI hydrate is thermodynamically stable, (4) the initial composition of C1-C2 sII hydrate at 268 K contains less than the original amount of C 1, (5) a quasi-liquid water layer solvating both C I and C2 exists at 268 K, (6) any C1(qll) and C2(qll) present at 253 K is too small to be detected, (7) the initial amounts of C1-C2 sI and sII hydrates formed at 253 K are much smaller than those formed at 268 and 274 K, and (8) Cl(aq), C2(aq) and C1(qll), C2(qll) facilitate the formation of C1-C2 sI and sII clathrate hydrate at 268 and 274 K, respectively. On the basis of these experimental observations, a model is developed that states that the aqueous hydration number of the most water-soluble clathrate hydrate former controls the structure of the clathrate hydrate that forms during the initial stages of the clathrate hydrate formation reaction. For methane-ethane clathrate hydrate, this means that ethane in a water liquid phase or quasi-liquid layer eliminates or adds two water molecules to its hydration shell to form the ethane-filled 5(12)6(2) or 5(12)6(4) cage building blocks of structure I or structure II clathrate hydrate, respectively. Density functional theory computations on methane-filled 5(12), ;5(12)6(2), and 5(12)6(4) and ethane-filled 5(12)6(2), 5(12)6(3), and 5(12)6(4) clathrate hydrate cages yield the stabilization energy of the gas-filled cages and provide theoretical evidence consistent with the experimentally based clathrate hydrate formation model. The proposed model is found to explain the results of other clathrate hydrate formation reactions.
引用
收藏
页码:12355 / 12361
页数:7
相关论文
共 47 条
[1]  
[Anonymous], 2000, THESIS COLORADO SCH
[2]   MECHANISMS AND KINETICS OF HYDRATE FORMATION [J].
CHRISTIANSEN, RL ;
SLOAN, ED .
INTERNATIONAL CONFERENCE ON NATURAL GAS HYDRATES, 1994, 715 :283-305
[3]  
Davidson D., 1973, Water in Crystalline Hydrates Aqueous Solutions of Simple Nonelectrolytes, P115
[4]  
DAVIDSON DW, 1986, GEOCHIM COSMOCHIM AC, V50, P619, DOI 10.1016/0016-7037(86)90110-9
[5]   Direct measure of the hydration number of aqueous methane [J].
Dec, SF ;
Bowler, KE ;
Stadterman, LL ;
Koh, CA ;
Sloan, ED .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (02) :414-415
[6]   NMR study of methane plus ethane structure I hydrate decomposition [J].
Dec, Steven F. ;
Bowler, Kristen E. ;
Stadterman, Laura L. ;
Koh, Carolyn A. ;
Sloan, E. Dendy, Jr. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2007, 111 (20) :4297-4303
[7]  
Elwell D, 1975, CRYSTAL GROWTH HIGH, P273
[8]   THERMOPHYSICAL PROPERTIES OF ETHANE [J].
FRIEND, DG ;
INGHAM, H ;
ELY, JF .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1991, 20 (02) :275-347
[9]   ANOMALOUS HEAT-CAPACITY OF HYDROPHOBIC SOLVATION [J].
GILL, SJ ;
DEC, SF ;
OLOFSSON, G ;
WADSO, I .
JOURNAL OF PHYSICAL CHEMISTRY, 1985, 89 (17) :3758-3761
[10]   Low-Frequency Electrical Properties of Polycrystalline Saline Ice and Salt Hydrates [J].
Grimm, Robert E. ;
Stillman, David E. ;
Dec, Steven F. ;
Bullock, Mark A. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (48) :15382-15390