Interaction Between the Cyclopentane Hydrate Particle and Water Droplet in Hydrocarbon Oil

被引:23
作者
Chen, Zihui [1 ]
Liu, Bo [1 ]
Manica, Rogerio [1 ]
Liu, Qingxia [1 ]
Xu, Zhenghe [1 ]
机构
[1] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 1H9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
SURFACTANT ADSORPTION; INTERFACIAL-TENSION; STABILITY; EMULSIONS; ASPHALTENES; COMPONENTS; BEHAVIOR; FILMS;
D O I
10.1021/acs.langmuir.9b03887
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The presence of immiscible water drops in bulk hydrocarbon is likely to bridge hydrate particles to cause hydrate agglomeration, leading to potential pipeline blockage. This can become a major challenge for flow assurance in offshore petroleum transportation. To avoid hydrate aggregation, the attachment between hydrate and water drops should be avoided. In this study, we used our home-designed integrated thin film drainage apparatus to investigate the interactions between a hydrate particle and a water drop inside model oil (i.e., mixture of cyclopentane and toluene with a volumetric ratio of 1:1). Our experiments showed that asphaltenes, a natural component in crude oil, were an effective inhibitor for the attachment between water drops and hydrate particles. Without asphaltenes in the system, the water drop adhered to the hydrate particle immediately after the two surfaces contacted. By adding 0.03 g/L asphaltenes into the oil phase, the attachment was delayed by 0.7 s when the applied preload force was set to around 0.05 mN. By increasing the asphaltenes addition to 0.05 g/L, the attachment between the hydrate and water drop was prevented even when the contact time lasted up to 25 s. This phenomenon could be explained by the adsorption of an asphaltenes layer along the interface between the aqueous drop and hydrocarbon. Measurements of the dynamic interfacial tension and trumping ratio confirmed the presence of the adsorption layer. The addition of 0.6 mol/L NaCl or 0.3 mol/L CaCl2 in the aqueous drop could further enhance the strength of the adsorption layer. Results of this research provide understanding of the benefits of asphaltenes and salt in preventing hydrate agglomeration.
引用
收藏
页码:2063 / 2070
页数:8
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[1]   Surfactant Adsorption and Interfacial Tension Investigations on Cyclopentane Hydrate [J].
Aman, Zachary M. ;
Olcott, Kyle ;
Pfeiffer, Kristopher ;
Sloan, E. Dendy ;
Sum, Amadeu K. ;
Koh, Carolyn A. .
LANGMUIR, 2013, 29 (08) :2676-2682
[2]   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
[3]  
[Anonymous], CLATHRATE HYDRATES N
[4]   Adhesion force between cyclopentane hydrates and solid surface materials [J].
Aspenes, G. ;
Dieker, L. E. ;
Aman, Z. M. ;
Hoiland, S. ;
Sum, A. K. ;
Koh, C. A. ;
Sloan, E. D. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2010, 343 (02) :529-536
[5]   Influence of Interaction Between Heavy Oil Components and Petroleum Sulfonate on the Oil-Water Interfacial Tension [J].
Bai, Jin-Mei ;
Fan, Wei-Yu ;
Nan, Guo-Zhi ;
Li, Shui-Ping ;
Yu, Bao-Shi .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 2010, 31 (04) :551-556
[6]   Accurate description of phase diagram of clathrate hydrates at the molecular level [J].
Belosludov, Rodion V. ;
Subbotin, Oleg S. ;
Mizuseki, Hiroshi ;
Kawazoe, Yoshiyuki ;
Belosludov, Vladimir R. .
JOURNAL OF CHEMICAL PHYSICS, 2009, 131 (24)
[7]   Interfacial tension of bitumen-water interfaces. Part 1: Influence of endogenous surfactants at acidic pH [J].
Chaverot, P. ;
Cagna, Alain ;
Glita, Sylvie ;
Rondelez, Francis .
ENERGY & FUELS, 2008, 22 (02) :790-798
[8]   Review of natural gas hydrates as an energy resource: Prospects and challenges [J].
Chong, Zheng Rong ;
Yang, She Hern Bryan ;
Babu, Ponnivalavan ;
Linga, Praveen ;
Li, Xiao-Sen .
APPLIED ENERGY, 2016, 162 :1633-1652
[9]  
Demir A. B., 2016, SPE W REG M
[10]   Surface tension isotherms for surfactant adsorption layers including surface aggregation [J].
Fainerman, VB ;
Miller, R .
LANGMUIR, 1996, 12 (25) :6011-6014