NMR based experiment of fluid invasion to natural gas hydrate reservoir and hydrate dissociation inhibition mechanism

被引:4
作者
Shao, Zihua [1 ]
Wang, Jintang [1 ,2 ,4 ]
Lv, Kaihe [1 ]
Wang, Zonglun [1 ]
Bai, Yujing [1 ]
Wang, Ren [3 ]
Sun, Jinsheng [1 ,3 ]
机构
[1] China Univ Petr East China, Sch Petr Engn, Qingdao 266580, Shandong, Peoples R China
[2] Minist Educ, Key Lab Unconvent Oil & Gas Dev, Qingdao 266580, Peoples R China
[3] CNPC Engn Technol R&D Co Ltd, Beijing 102206, Peoples R China
[4] China Univ Petr East China, Dept Petr Engn, Qingdao 266580, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Natural gas hydrate; NMR-based method; Invasion mechanism; Hydrate dissociation inhibition; BEARING SEDIMENTS; HEAT-TRANSFER;
D O I
10.1016/j.fuel.2023.129372
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
Hydrate dissociation inhibition has an important bearing on drilling safety for natural gas hydrate exploitation. A low-field NMR-based experimental method is developed for characterizing the hydrate dissociation inhibition effect during fluid invasion to hydrate-bearing sediment. The hydrate core sample is prepared by excess-gas method, and deionized water or hydrate dissociation inhibitor solution was injected at constant flow rate. In the presence of hydrate dissociation inhibitor, the invasion area is significantly reduced, and invasion fluid saturation was kept at 30 % instead of 80 % compared to water. Experimental techniques were used to reveal hydrate dissociation inhibition mechanism. Hydrate dissociation inhibitor at 1 % can reduce the thermal conductivity of aqueous solution from 0.5870 W center dot m(-1)center dot K-1 to 0.5710 W center dot m(-1)center dot K-1 at 4 degrees C, and increase the lowtemperature apparent viscosity from 1 mPa center dot s to 10 mPa center dot s, reducing the heat and mass transfer ability of drilling fluid with hydrate reservoirs. The surface tension of water was decreased from 72.8 mN center dot m(-1) to 59.94 mN center dot m(-1), which is conducive to the multi-point adsorption of inhibitors at the hydrate interface. The water activity was reduced from 1.000 to 0.985, showing little effect on the equilibrium temperature of hydrate phase. This work showcases the significance of hydrate dissociation inhibition during fluid invasion to hydrate-bearing sediment.
引用
收藏
页数:9
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