Depressurization-induced gas production from class 1 hydrate deposits

被引:312
作者
Moridis, George J. [1 ]
Kowalsky, Michael B. [1 ]
Pruess, Karsten [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Earth Sci, Dept Hydrogeol, Berkeley, CA 94720 USA
关键词
D O I
10.2118/97266-PA
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
Class 1 hydrate deposits are characterized by a hydrate-bearing layer underlain by a two-phase zone involving mobile gas. Two kinds of deposits are investigated. The first involves water and hydrate in the hydrate zone (Class I W), while the second involves gas and hydrate (Class 1G). We introduce new models to describe the effect of the presence of hydrates on the wettability properties of porous media. We determine that large volumes of gas can be readily produced at high rates for long times from Class 1 gashydrate accumulations by means of depressurization-induced dissociation using conventional technology. Dissociation in Class 1W deposits proceeds in distinct stages, while it is continuous in Class 1G deposits. To avoid blockage caused by hydrate formation in the vicinity of the well, wellbore heating is a necessity in production from Class I hydrates. Class 1W hydrates are shown to contribute up to 65% of the production rate and up to 45% of the cumulative volume of produced gas; the corresponding numbers for Class I G hydrates are 75% and 54%. Production from both Class 1W and Class 1G deposits leads to the emergence of a second dissociation front (in addition to the original ascending hydrate interface) that forms at the top of the hydrate interval and advances downward. In both kinds of deposits, capillary pressure effects lead to hydrate lensing (i.e., the emergence of distinct banded structures of alternating high/low hydrate saturation, which form channels and shells and have a significant effect on production).
引用
收藏
页码:458 / 481
页数:24
相关论文
共 30 条
[1]  
Bejan A., 1984, CONVECTION HEAT TRAN
[2]  
Brooks R.H., 1966, J. Irrig. Drain. Div.-ASCE, V92, P61
[3]   Determination of the intrinsic rate of ethane gas hydrate decomposition [J].
Clarke, M ;
Bishnoi, PR .
CHEMICAL ENGINEERING SCIENCE, 2000, 55 (21) :4869-4883
[4]  
Dallimore S.R., 1999, GEOL SURV CAN BULL, V544, P1
[5]  
Holder G.D., 1982, SPE, V11105, DOI [10.2118/11105-MS, DOI 10.2118/11105-MS]
[6]   KINETICS OF METHANE HYDRATE DECOMPOSITION [J].
KIM, HC ;
BISHNOI, PR ;
HEIDEMANN, RA ;
RIZVI, SSH .
CHEMICAL ENGINEERING SCIENCE, 1987, 42 (07) :1645-1653
[7]   Comparison of kinetic and equilibrium reaction models in simulating gas hydrate behavior in porous media [J].
Kowalsky, Michael B. ;
Moridis, George J. .
ENERGY CONVERSION AND MANAGEMENT, 2007, 48 (06) :1850-1863
[8]  
KURIHARA M, 2005, SCI RESULTS MALLIK 2, V585
[9]  
Kurihara M., 2005, 5 INT C GAS HYDRATES
[10]  
Leverett MC, 1941, T AM I MIN MET ENG, V142, P152, DOI 10.2118/941152-G