Optimum phase-behavior formulation of surfactant/oil/water systems for the determination of chromium in heavy crude oil and in bitumen-in-water emulsion

被引:26
作者
Burguera, JL
Avila-Gómez, RM
Burguera, M
de Salager, RA
Salager, JL
Bracho, CL
Burguera-Pascu, M
Burguera-Pascu, C
Brunetto, R
Gallignani, M
de Pefia, YP
机构
[1] Univ Los Andes, IVAIQUIM, Fac Sci, Merida 5101A, Venezuela
[2] Univ Los Andes, FIRP, Fac Engn, Merida 5101, Venezuela
[3] Univ Los Andes, Fac Odontol, Merida 5101, Venezuela
关键词
heavy crude oils; three-phase behavior; ET AAS; chromium;
D O I
10.1016/S0039-9140(03)00275-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An "oil in water" formulation was optimized to determine chromium in heavy crude oil (HCO) and bitumen-in-water emulsion (Orimulsion-400(R)) samples by transversally heated electrothermal atomic absorption spectrometry (TH-ET AAS) using Zeeman effect background correction. The optimum proportion of the oil-water mixture ratio was 7:3 v/v (70 ml of oil as the internal phase) with a non-ionic surfactant concentration (Intan-100) in the emulsion of 0.2% w/w. Chromium was deter-mined in different crude oil samples after dilution of the emulsions 1:9 v/v with a 0.2% w/w solution of surfactant in order to further reduce the viscosity from 100 to 1.6 cP and at the same time to bring the concentration of chromium within the working range of the ET AAS technique. The calibration graph was linear from 1.7 to 100 mug Cr l(-1). The sensitivity was of 0.0069 s 1 mug(-1), the characteristic mass (m(o)) was of 5.7 pg per 0.0044 s and the detection limit (3sigma) was of 0.52 mug l(-1). The relative standard deviation of the method, evaluated by replicate analyses of three crude oil samples varied in all cases between 1.5 and 2.6%. Recovery studies were performed on four Venezuelan crude oils, and the average chromium recovery values varied between 95.9-104.8, 90.6-107.6, 95.6-104.0 and 98.8-103.9% for the Cerro Negro, Crudo Hamaca and Boscan crude oils and for the Orimulsion(R)-400, respectively. The results obtained in this work for the Cerro Negro, Crudo Hamaca and Boscan crude oils and for the Orimulsion(R)-400 following the proposed procedure were of 0.448 +/- 0.008, 0.338 +/- 0.004 0.524 +/- 0.021 and 0.174 +/- 0.008 mg Cr l(-1), respectively, which were in good agreement with the values obtained by a tedious recommended standard procedure (respectively: 0.470 +/- 0.05, 0.335 +/- 0.080, 0.570 +/- 0.021 and 0.173 +/- 0.009 mg Cr l(-1)). (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:353 / 361
页数:9
相关论文
共 31 条
[11]  
FILBY RH, 1975, ROLE TRACE METALS PE
[12]  
*I PETR, 1990, STAND METH AN TEST P, V2
[13]   PRE-CONCENTRATION AND X-RAY-FLUORESCENCE DETERMINATION OF VANADIUM, NICKEL AND IRON IN RESIDUAL FUEL OILS AND IN PARTICULATE MATERIAL FROM OIL-FIRED SOURCES [J].
IWASAKI, K ;
TANAKA, K .
ANALYTICA CHIMICA ACTA, 1982, 136 (APR) :293-299
[14]   Determination of trace elements in naphtha by inductively coupled plasma mass spectrometry using water-in-oil emulsions [J].
Kumar, SJ ;
Gangadharan, S .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1999, 14 (06) :967-971
[15]   FOAMING PROPERTIES OF SURFACTANT-OIL-WATER SYSTEMS IN THE NEIGHBORHOOD OF OPTIMUM FORMULATION [J].
LACHAISE, J ;
BREUL, T ;
GRACIAA, A ;
MARION, G ;
MONSALVE, A ;
SALAGER, JL .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 1990, 11 (05) :443-453
[16]  
LAYRISSE I, 1984, REV TEC INTEVEP, V4, P3
[17]   DETERMINATION OF TRACE-METALS IN CRUDE-OIL BY INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY WITH MICROEMULSION SAMPLE INTRODUCTION [J].
LORD, CJ .
ANALYTICAL CHEMISTRY, 1991, 63 (15) :1594-1599
[18]   The utility of a W-Ir permanent chemical modifier for the determination of Ni and V in emulsified fuel oils and naphtha by transverse heated electrothermal atomic absorption spectrometer [J].
Meeravali, NN ;
Kumar, SJ .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (05) :527-532
[19]  
MILLER JN, 2000, STAT CHEMOMETRIC ANA
[20]   Miniemulsion formation by transitional inversion [J].
Miñana-Perez, M ;
Gutron, C ;
Zundel, C ;
Anderez, JM ;
Salager, JL .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 1999, 20 (03) :893-905