Role of Water on the Precipitation and Deposition of Asphaltenes in Packed-Bed Microreactors

被引:23
作者
Hu, Chuntian [1 ]
Sabio, Jasmine C. [1 ]
Yen, Andrew [2 ]
Joshi, Nikhil [3 ]
Hartman, Ryan L. [1 ]
机构
[1] Univ Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
[2] Nalco Champ, Sugar Land, TX 77478 USA
[3] Anadarko Petr Corp, The Woodlands, TX 77380 USA
关键词
ALKYLBENZENE-DERIVED AMPHIPHILES; COLLOIDAL PARTICLES; TEMPERATURE-RANGE; AGGREGATION; STABILIZATION; PERMEABILITY; DISSOLUTION; KINETICS; CLASSIFICATION; SOLUBILITY;
D O I
10.1021/ie5038775
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Water naturally comprises some fraction of virtually all petroleum reservoirs worldwide, yet its existence introduces complexity to asphaltene precipitation and deposition mechanisms. This global problem not only impacts upstream conventional and unconventional energy production but also influences downstream chemical refining, the construction industry, and the transportation sector. A transparent packed-bed microreactor (mu PBR) with inline analytics was designed to merge two fields of science, oilfield chemistry and microchemical systems, to investigate the role of water on the molecular-to-the-microscale deposition of asphaltenes in quartz porous media. Porosity loss and permeability impairment of the porous media for water mass fractions of <0:001 to 34.5 wt % were investigated. Interestingly, a switch in the mechanism of water (from 0.030 to 3.18 wt %) on the accumulation was discovered. Analyses of porosity permeability relationships revealed competition between adsorption and desorption followed by pore throat plugging via mechanical entrapment for all mass fractions of water studied. Soluble water molecules were also found to decrease the asphaltene nanopartide collision efficiency within quartz porous Media where trace amounts existed (i.e., in the range of <0.001 to 0.030 wt % water), whereas higher mass fractions (>0.030 wt %) created the possibility of emulsion water blocking with more particles (relatively speaking) depositing on pore throat surfaces, precipitating by heterogeneous nucleation at asphaltene-water interfaces and/or experiencing catalyzed nanoaggregation at interfaces. In general, the water fraction was found to control the number of closed pore throats that interconnect the quartz porous media. Transparent packed-bed microreactors that bridge molecular-to-microscale understanding of asphaltene water interactions are promising as tools for the advancement of asphaltene science and risk management during hydrocarbon production.
引用
收藏
页码:4103 / 4112
页数:10
相关论文
共 69 条
[1]   Viscosity of N-pentane, N-heptane and their mixtures within the temperature range from 298 degrees K up to critical points at the saturation vapor pressure [J].
Abdulagatov, IM ;
Rasulov, SM .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1996, 100 (02) :148-154
[2]   Asphaltene precipitation and deposition in the near wellbore region: a modeling approach [J].
Almehaideb, RA .
JOURNAL OF PETROLEUM SCIENCE AND ENGINEERING, 2004, 42 (2-4) :157-170
[3]   Molecular Orientation of Asphaltenes and PAH Model Compounds in Langmuir-Blodgett Films Using Sum Frequency Generation Spectroscopy [J].
Andrews, A. Ballard ;
McClelland, Arthur ;
Korkeila, Oona ;
Demidov, Alexander ;
Krummel, Amber ;
Mullins, Oliver C. ;
Chen, Zhan .
LANGMUIR, 2011, 27 (10) :6049-6058
[4]  
[Anonymous], P SPE INT S FORM DAM
[5]  
[Anonymous], GEOPHYS RES LETT
[6]  
[Anonymous], ENCY POLYM SCI ENG
[7]  
[Anonymous], 2007, ASPHALTENES HEAVY OI
[8]   Dispersant adsorption during asphaltene aggregation studied by fluorescence resonance energy transfer (FRET) [J].
Arteaga-Larios, F ;
Cosultchi, A ;
Pérez, E .
ENERGY & FUELS, 2005, 19 (02) :477-484
[9]   The viscosity of toluene in the temperature range from 210 to 370 K at pressures up to 30 MPa [J].
Assael, MJ ;
Dalaouti, NK ;
Polimatidou, S .
INTERNATIONAL JOURNAL OF THERMOPHYSICS, 1999, 20 (05) :1367-1377
[10]   Structure and collapse of particle monolayers under lateral pressure at the octane/aqueous surfactant solution interface [J].
Aveyard, R ;
Clint, JH ;
Nees, D ;
Quirke, N .
LANGMUIR, 2000, 16 (23) :8820-8828