Spontaneous generation of stable CO2 emulsions via the dissociation of nanoparticle-aided CO2 hydrate

被引:8
作者
Kim, Seunghee [1 ]
Zadeh, Amin Hosseini [1 ]
Nole, Michael [2 ]
Daigle, Hugh [3 ]
Huh, Chun [3 ]
Kim, Ijung [4 ]
机构
[1] Univ Nebraska Lincoln, Dept Civil & Environm Engn, Omaha, NE 68182 USA
[2] Sandia Natl Labs, Albuquerque, NM 87123 USA
[3] Univ Texas Austin, Dept Petr & Geosyst Engn, Austin, TX 78712 USA
[4] Hongik Univ, Dept Civil & Environm Engn, Seoul, South Korea
关键词
Gas hydrate; Carbon dioxide; Nanoparticles; Emulsion; Foam; CO2; utilization; IN-WATER EMULSIONS; SILICA NANOPARTICLES; MOLECULAR-DYNAMICS; GAS; DIOXIDE; SURFACTANTS; METHANE; STORAGE; FOAMS; CONVERSION;
D O I
10.1016/j.petrol.2021.109203
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 study finds that CO2 hydrate dissociation spontaneously generates fine-textured emulsions or foams, and that the phase state of CO2 which was used to form hydrate determines the stability of the emulsion or foam when hydrate is dissociated in an aqueous dispersion of hydrophilic silica nanoparticles. This process suggests an energy-efficient method of generating stable emulsions for high-pressure applications without a need for mechanical energy input. We proved experimentally that the CO2 hydrate phase could be used to generate foams and emulsions because the hydrate formation process naturally disconnects a hydrate guest molecule phase from the bulk water phase. During dissociation, easy adsorption of nanoparticles at CO2-water interfaces hinders the coalescence of bubbles. As a result, CO2 emulsions or foams were generated upon the completion of hydrate dissociation. The CO2 emulsions generated remained fairly stable, while the CO2 foams generated became unstable and the buoyant force of the CO2 bubbles led to their coalescence. The concepts experimentally proven here could be applicable to any suitable clathrate compound undergoing a solid to a liquid phase transition.
引用
收藏
页数:8
相关论文
共 48 条
[1]   Immiscible Foam for Enhancing Oil Recovery: Bulk and Porous Media Experiments [J].
Andrianov, A. ;
Farajzadeh, R. ;
Nick, M. Mahmoodi ;
Talanana, M. ;
Zitha, P. L. J. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2012, 51 (05) :2214-2226
[2]   Surface modification of silica nanoparticles to reduce aggregation and nonspecific binding [J].
Bagwe, RP ;
Hilliard, LR ;
Tan, WH .
LANGMUIR, 2006, 22 (09) :4357-4362
[3]   Microsecond Molecular Dynamics Simulations of the Kinetic Pathways of Gas Hydrate Formation from Solid Surfaces [J].
Bai, Dongsheng ;
Chen, Guangjin ;
Zhang, Xianren ;
Wang, Wenchuan .
LANGMUIR, 2011, 27 (10) :5961-5967
[4]   Oil-in-Water Emulsions for Encapsulated Delivery of Reactive Iron Particles [J].
Berge, Nicole D. ;
Ramsburg, C. Andrew .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (13) :5060-5066
[5]  
Binks Bernard P., 2006, COLLOIDAL PARTICLES
[6]   Aqueous foams stabilized solely by silica nanoparticles [J].
Binks, BP ;
Horozov, TS .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (24) :3722-3725
[7]   Particles as surfactants - similarities and differences [J].
Binks, BP .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2002, 7 (1-2) :21-41
[8]  
Blasco J, 2016, MARINE ECOTOXICOLOGY: CURRENT KNOWLEDGE AND FUTURE ISSUES, P1
[9]   CO2/water interfacial tensions under pressure and temperature conditions of CO2 geological storage [J].
Chiquet, Pierre ;
Daridon, Jean-Luc ;
Broseta, Daniel ;
Thibeau, Sylvain .
ENERGY CONVERSION AND MANAGEMENT, 2007, 48 (03) :736-744
[10]   Effect of surfactants on the interfacial tension and emulsion formation between water and carbon dioxide [J].
da Rocha, SRP ;
Harrison, KL ;
Johnston, KP .
LANGMUIR, 1999, 15 (02) :419-428