Study of the ion exchange selectivity of layered titanosilicate Na3(Na,H)Ti2O2[Si2O6]2 • 2H2O, AM-4, for strontium

被引:15
作者
Decaillon, JG
Andrès, Y
Mokili, BM
Abbé, JC
Tournoux, M
Patarin, J
机构
[1] GEPEA, Ecole Mines Nantes, F-44070 Nantes 03, France
[2] Univ Nantes, CNRS UMR 6457, Ecole Mines Nantes, Lab Subatech, Nantes 03, France
[3] IRCCyN, Delegat CNRS, F-44321 Nantes 03, France
[4] Inst Mat Jean Rouxel, Lab Chim Solides, F-44072 Nantes 03, France
[5] CNRS, UPRES A 7016, Lab Mat Mineraux, F-68093 Mulhouse, France
关键词
D O I
10.1081/SEI-120003027
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper describes for the first time the sorption behaviour of a titanosilicate, AM-4, that exhibits an extremely high affinity for strontium in neutral and alkaline media. The ion exchange selectivity of this layered titanosilicate is explained in relation to the crystalline structure. The simple approach which consists in studying carefully the distribution of formal charges of oxygens in the anionic framework and calculating a normalized bond length in order to measure the ion stability in its site has enabled us to account for the AM-4 performances for the strontium remediation in competition with alkali and alkaline earth metal ions, The Sr uptake amounts as a function of the pH were determined, they can be correlated to the formal charges of Si-O-nbo. The effect of sodium, potassium, calcium and magnesium on the Sr2+ ions sorption was also studied in binary solutions Sr2+/Na+, Sr2+/K+, Sr2+/Ca2+, Sr2+/Mg2+. The determination of the equilibrium constant Sr2+/2Na(+) and of the ion competitive effects with adsorption data have shown that Ca2+ is the most efficient to reduce the uptake of Sr2+. The preliminary Kd values provide an indication that this exchanger may act as a sorber for groundwater and nuclear remediation applications.
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页码:273 / 291
页数:19
相关论文
共 26 条
[1]  
Aimin Z, 1995, J RADIOANAL NUCL CHE, V198, P375
[2]  
Anthony R. G., 1993, Waste Management, V13, P503, DOI 10.1016/0956-053X(93)90080-G
[3]   Syntheses, X-ray powder structures, and preliminary ion-exchange properties of germanium-substituted titanosilicate pharmacosiderites:: HM3(AO)4(BO4)3•4H2O (M = K, Rb, Cs; A = Ti, Ge; B = Si, Ge) [J].
Behrens, EA ;
Poojary, DM ;
Clearfield, A .
CHEMISTRY OF MATERIALS, 1998, 10 (04) :959-967
[4]   Assessment of a sodium nonatitanate and pharmacosiderite-type ion exchangers for strontium and cesium removal from DOE waste simulants [J].
Behrens, EA ;
Sylvester, P ;
Clearfield, A .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (01) :101-107
[5]   Evaluation of synthetic inorganic ion exchangers for cesium and strontium removal from contaminated groundwater and wastewater [J].
Bortun, AI ;
Bortun, LN ;
Clearfield, A .
SOLVENT EXTRACTION AND ION EXCHANGE, 1997, 15 (05) :909-929
[6]   Ion exchange properties of the sodium phlogopite and biotite [J].
Bortun, AI ;
Bortun, LN ;
Khainakov, SA ;
Clearfield, A .
SOLVENT EXTRACTION AND ION EXCHANGE, 1998, 16 (04) :1067-1090
[7]   THERMODYNAMIC PROPERTIES OF STRONG ELECTROLYTES IN AQUEOUS-SOLUTIONS [J].
BROMLEY, LA .
AICHE JOURNAL, 1973, 19 (02) :313-320
[8]   LOCAL-STRUCTURE OF ALKALINE-EARTH BOROALUMINATE CRYSTALS AND GLASSES .1., CRYSTAL CHEMICAL CONCEPTS STRUCTURAL PREDICTIONS AND COMPARISONS TO KNOWN CRYSTAL-STRUCTURES [J].
BUNKER, BC ;
KIRKPATRICK, RJ ;
BROW, RK .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1991, 74 (06) :1425-1429
[9]  
BUNKER BC, 1994, TWRSPP94085 PAC NW L, P1
[10]   PREPARATION, STRUCTURE, AND ION-EXCHANGE PROPERTIES OF NA4TI9O20.XH2O [J].
CLEARFIELD, A ;
LEHTO, J .
JOURNAL OF SOLID STATE CHEMISTRY, 1988, 73 (01) :98-106