Breaking of Water-in-Crude-Oil Emulsions. 3. Influence of Salinity and Water-Oil Ratio on Demulsifier Action

被引:74
作者
Borges, Belsay [2 ]
Rondon, Miguel [1 ]
Sereno, Onelys
Asuaje, Juan
机构
[1] Univ Simon Bolivar, Dept Termodinam & Fenomenos Transferencia, Caracas 1080 A, Venezuela
[2] Univ Simon Bolivar, Dept Quim, Caracas 1080 A, Venezuela
关键词
AFFINITY INVERSION; PHASE-BEHAVIOR; SURFACTANT; SYSTEMS; FORMULATION; STABILITY; ASPHALTENES; INTERFACE; SIZE;
D O I
10.1021/ef8008822
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
The stability of water-in-diluted-crude-oil emulsions is found to depend upon the water-phase salinity and the water-oil ratio for different asphaltene and demulsifier concentrations. It is reported that the most stable emulsions are formed when one of the phase volumes largely exceeds the other and that the minimum stability is found at the formulation for which the emulsion inversion takes place. For asphaltene concentrations over 500 ppm, this occurs at a volumetric fraction between 0.3 and 0.7 and, in this range, the higher the water-phase content, the lower the required demulsifier concentration. It is also determined that there is an optimum value of the demulsifier concentration that promotes the fastest separation. At a fixed asphaltene concentration, an increase in salinity generally leads to a lower demulsifier requirement. Finally, at higher asphaltene concentrations, simultaneous increases in salinity and demulsifier concentration are required to attain an optimal rate of emulsion breaking.
引用
收藏
页码:1568 / 1574
页数:7
相关论文
共 36 条
[1]   Asphaltenes and other natural Surfactants from cerro Negro crude oil. Stepwise adsorption at the water/toluene interface: Film formation and hydrophobic effects [J].
Acevedo, S ;
Borges, B ;
Quintero, F ;
Piscitelly, V ;
Gutierrez, LB .
ENERGY & FUELS, 2005, 19 (05) :1948-1953
[2]   Apparent equilibration time required for surfactant-oil-water systems to emulsify into the morphology imposed by the formulation.: Part 2:: Effect of sec-butanol concentration and initial location [J].
Alvarez, G ;
Antón, R ;
Marfisi, S ;
Márquez, L ;
Salager, JL .
LANGMUIR, 2004, 20 (13) :5179-5181
[3]  
ANGLE CW, 2001, ENCY HDB EMULSION TE, V24, P541
[4]  
[Anonymous], J COLLOID INTERFACE
[5]   EMULSION INSTABILITY IN THE 3-PHASE BEHAVIOR REGION OF SURFACTANT ALCOHOL OIL BRINE SYSTEMS [J].
ANTON, RE ;
SALAGER, JL .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1986, 111 (01) :54-59
[6]   The theory of emulsification, V [J].
Bancroft, WD .
JOURNAL OF PHYSICAL CHEMISTRY, 1913, 17 (06) :501-519
[7]   A CORRELATION FOR PHASE-BEHAVIOR OF NON-IONIC SURFACTANTS [J].
BOURREL, M ;
SALAGER, JL ;
SCHECHTER, RS ;
WADE, WH .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1980, 75 (02) :451-461
[8]   FACTORS AFFECTING EMULSION STABILITY, AND HLB CONCEPT [J].
BOYD, J ;
SHERMAN, P ;
PARKINSONL, C .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1972, 41 (02) :359-+
[9]   DYNAMICS OF LIQUID LIQUID-PHASE INVERSION USING NONIONIC SURFACTANTS [J].
BROOKS, BW ;
RICHMOND, HN .
COLLOIDS AND SURFACES, 1991, 58 (1-2) :131-148
[10]  
DAVIS HT, 1993, P WORLD C EM PAR FRA, V4, P69