Third phase formation revisited:: The U(VI), HNO3-TBP, n-dodecane system

被引:138
作者
Chiarizia, R
Jensen, MP
Borkowski, M
Ferraro, JR
Thiyagarajan, P
Littrell, KC
机构
[1] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[2] Argonne Natl Lab, IPNS Div, Argonne, IL 60439 USA
关键词
third phase formation; tributylphosphate; uranyl nitrate; small angle neutron; scattering; EXAFS;
D O I
10.1081/SEI-120017545
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, the system U(VI), HNO3-tri-n-butylphosphate (TBP), n-dodecane has been revisited with the objective of gaining information on the coordination chemistry and structural evolution of the species formed in the organic phase before and after third phase formation. Chemical analyses, spectroscopic and EXAFS data indicate that U(VI) is extracted as the UO2(NO3)(2).2TBP adduct, while the third phase species have the average composition UO2(NO3)(2).2TBP.HNO3. Small-angle neutron scattering (SANS) measurements on TBP solutions loaded with only HNO3 or with increasing amounts of U(VI) have revealed the presence, before phase splitting, of ellipsoidal aggregates with the major and minor axes up to about 64 and 15 Angstrom, respectively. The formation of these aggregates, very likely of the reverse micelle-type, is observed in all cases, that is, when only HNO3, only UO2(NO3)(2), or both HNO3 and UO2(NO3)(2) are extracted by the TBP solution. Upon third phase formation, the SANS data reveal the presence of smaller aggregates in the light organic phase, while the heavy organic phase contains pockets of diluent, each with an average of about two molecules of n-dodecane.
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页码:1 / 27
页数:27
相关论文
共 53 条
[41]  
Osseo-Asare K., 2002, P INT SOLV EXTR C IS, P118
[42]   AGGREGATION, REVERSED MICELLES, AND MICROEMULSIONS IN LIQUID-LIQUID-EXTRACTION - THE TRI-NORMAL-BUTYL PHOSPHATE-DILUENT-WATER-ELECTROLYTE SYSTEM [J].
OSSEOASARE, K .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 1991, 37 (1-2) :123-173
[43]   VOLUME CHANGES AND DISTRIBUTION OF HCL AND H2O IN THE TRI-N-BUTYL PHOSPHATE H2O-HCL LIQUID LIQUID-SYSTEM - A REVERSED MICELLAR PHENOMENOLOGICAL MODEL [J].
OSSEOASARE, K .
COLLOIDS AND SURFACES, 1990, 50 :373-392
[44]   Analysis of small-angle scattering data from colloids and polymer solutions: modeling and least-squares fitting [J].
Pedersen, JS .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 1997, 70 :171-210
[45]   THE PREPARATION AND INFRA-RED ABSORPTION SPECTRA OF SEVERAL COMPLEXES OF BIS-(2-ETHYLHEXYL)-PHOSPHORIC ACID [J].
PEPPARD, DF ;
FERRARO, JR .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1959, 10 (3-4) :275-288
[46]   A review of third phase formation in extraction of actinides by neutral organophosphorus extractants [J].
Rao, PRV ;
Kolarik, Z .
SOLVENT EXTRACTION AND ION EXCHANGE, 1996, 14 (06) :955-993
[47]  
Schaekers J. M., 1991, SCI TECHNOLOGY TRIBU, VIV, P71
[48]  
Solovkin AS, 1960, RUSS J INORG CHEM, V5, P1026
[49]   THE PHYSIOCOCHEMICAL PROPERTIES OF PURE NITRIC ACID [J].
STERN, SA ;
MULLHAUPT, JT ;
KAY, WB .
CHEMICAL REVIEWS, 1960, 60 (02) :185-207
[50]   The time-of-flight small-angle neutron diffractometer (SAD) at IPNS, Argonne National Laboratory [J].
Thiyagarajan, P ;
Epperson, JE ;
Crawford, RK ;
Carpenter, JM ;
Klippert, TE ;
Wozniak, DG .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1997, 30 :280-293