Experimental determination of Ni isotope fractionation during Ni adsorption from an aqueous fluid onto calcite surfaces

被引:18
作者
Alvarez, Cristina Castillo [1 ]
Quitte, Ghylaine [2 ]
Schott, Jacques [1 ]
Oelkers, Eric H. [1 ,3 ,4 ]
机构
[1] Univ Toulouse, GET, CNRS, UMR 5563, F-31400 Toulouse, France
[2] Univ Toulouse, CNES, UPS, CNRS,UMR 5277,IRAP, F-31400 Toulouse, France
[3] UCL, London Geochem & Isotope Ctr LOGIC, Gower Pl, London, England
[4] Birkbeck Univ London, Gower Pl, London, England
关键词
Nickel isotopes; Calcite; Adsorption; X-RAY-DIFFRACTION; ZN2+ ADSORPTION; NICKEL; SORPTION; CARBONATE; FE; BIRNESSITE; SPECIATION; COMPLEXES; BORON;
D O I
10.1016/j.gca.2020.01.010
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The fractionation of Ni isotopes during Ni adsorption from aqueous fluids onto calcite surfaces was measured at 25 degrees C and as a function of pH from 7.7 to 8.9. Experiments showed that the percent Ni adsorbed and the degree of Ni isotope fractionation attained constant values in less than 30 hours after the calcite was exposed to the Ni bearing, calcite saturated aqueous solution. The percentage of Ni adsorbed from the fluid onto the calcite surfaces increased from 9 to 67% as the pH increased over this range. Calcite preferentially adsorbs light Ni isotopes during adsorption, resulting in a fractionation between adsorbed and aqueous, Delta Ni-60(calcite-fluid), of -0.52 +/- 0.16 parts per thousand. This value is pH independent, within uncertainty, over the experimental pH range. The preferential adsorption of light Ni isotopes into calcite likely results from the change in coordination environment between adsorbed and aqueous nickel; the Ni-O length in the Ni-CO3 bond formed at the calcite surface is greater than that in the Ni2+ aquo ion. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:26 / 36
页数:11
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