TY - JOUR
T1 - Novel nickel isolation procedure for a wide range of sample matrices without using dimethylglyoxime for isotope measurements using MC-ICP-MS
AU - Ratnayake, Dilan M.
AU - Tanaka, Ryoji
AU - Nakamura, Eizo
N1 - Funding Information:
The authors would like to thank members of the Pheasant Memorial Laboratory for the support in the laboratory, C. Sakaguchi and M. Yamanaka for helpful discussions and two anonymous reviewers for their constructive comments. We also thank K.C Hettiarachchi and H. Tripathi for improving the initial manuscript. Financial support for this project was provided by the Program for Promoting the Enhancement of Research University by MEXT and by JSPS KAKENHI grants ( 20K04108 ).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/10/9
Y1 - 2021/10/9
N2 - Nickel isotope ratios have traditionally been used as an important tracer in cosmochemistry, and recently, it has gained attention in geochemistry, biochemistry, and environmental sciences with the development of MC-ICP-MS. Purification of Ni before isotope measurement is mandatory for obtaining precise data, which has been commonly achieved with ion-exchange chromatography, employing dimethylglyoxime (DMG) as a chelating agent for Ni. However, it has been pointed out that the use of DMG can adversely affect the isotope measurement due to insufficient Ni recovery and mass bias during measurement caused by the remaining DMG. Ni isolation procedures without the usage of DMG were innovated, but they have disadvantages such as the necessity of complex separation methods, high Ni blank, and matrix-dependent Ni recovery. Here, we present a simple Ni isolation procedure without using DMG but with the aid of oxalic acid along with common inorganic acids, achieving near-complete recovery of Ni with low blanks [0.7 ± 0.3 ng (2SD, n = 4)] only using three ion exchange column steps. To validate our method and strengthen the Ni isotope database of reference materials, 60Ni/58Ni of 20 geological reference materials, covering wide matrix compositions, were measured by MC-ICP-MS using the double-spike method. The results have shown that high recovery of Ni, independent of the sample matrix elements was achieved (98 ± 4%) and the 60Ni/58Ni was measured with a 2SD of 0.006–0.084‰ from samples containing 100–200 ng Ni.
AB - Nickel isotope ratios have traditionally been used as an important tracer in cosmochemistry, and recently, it has gained attention in geochemistry, biochemistry, and environmental sciences with the development of MC-ICP-MS. Purification of Ni before isotope measurement is mandatory for obtaining precise data, which has been commonly achieved with ion-exchange chromatography, employing dimethylglyoxime (DMG) as a chelating agent for Ni. However, it has been pointed out that the use of DMG can adversely affect the isotope measurement due to insufficient Ni recovery and mass bias during measurement caused by the remaining DMG. Ni isolation procedures without the usage of DMG were innovated, but they have disadvantages such as the necessity of complex separation methods, high Ni blank, and matrix-dependent Ni recovery. Here, we present a simple Ni isolation procedure without using DMG but with the aid of oxalic acid along with common inorganic acids, achieving near-complete recovery of Ni with low blanks [0.7 ± 0.3 ng (2SD, n = 4)] only using three ion exchange column steps. To validate our method and strengthen the Ni isotope database of reference materials, 60Ni/58Ni of 20 geological reference materials, covering wide matrix compositions, were measured by MC-ICP-MS using the double-spike method. The results have shown that high recovery of Ni, independent of the sample matrix elements was achieved (98 ± 4%) and the 60Ni/58Ni was measured with a 2SD of 0.006–0.084‰ from samples containing 100–200 ng Ni.
KW - 3 column method
KW - Double spike method
KW - High recovery yield
KW - MC-ICP-MS
KW - Nickel isotope
KW - Oxalic acid
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U2 - 10.1016/j.aca.2021.338934
DO - 10.1016/j.aca.2021.338934
M3 - Article
C2 - 34556216
AN - SCOPUS:85112581860
SN - 0003-2670
VL - 1181
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
M1 - 338934
ER -