TY - JOUR

T1 - A new digestion and chemical separation technique for rapid and highly reproducible determination of Lu/Hf and Hf isotope ratios in geological materials by mc-ICP-MS

AU - Bizzarro, Martin

AU - Baker, J.A.

AU - Ulfbeck, D.

PY - 2003/7/1

Y1 - 2003/7/1

N2 - A new digestion procedure and chemical separation technique has been developed for measurement of Lu/Hf and Hf isotope ratios that does not require high-pressure bombs or use of HF or HClO acids. Samples are digested in dilute HCl or HNO after flux-fusion at 1100 °C in the presence of lithium metaborate. High field strength elements (HFSE) and rare earth elements (REE) are separated from this solution by co-precipitation with iron hydroxide. The dissolved precipitate (in 2 mol l HCl) is loaded directly onto a standard cation exchange column which separates remaining sample matrix from the heavy REE (Lu+Yb), and the middle-light REE and HFSE (Hf). The middle-light REE and individual HFSE are then separated (10.5, 9 and 6 mol l HCl) using a miniaturized column containing TEVA spec resin which provides a REE-, Ti- and Zr-free Hf cut. This chemical separation scheme can also be readily adapted for isotopic analysis of the Sm-Nd system and/or the other HFSE (Ti, Zr). Total procedural blanks for this technique are <100 pg and <2 pg for Hf and Lu, respectively, even when digesting large (0.5 g) samples. We present data from replicate digestions of international rock reference materials which demonstrate this technique routinely reproduces Lu/Hf ratios to <0.2% (2s) and 176Hf/177Hf isotope ratios to <30 ppm (2s). Moreover, the technique is matrix-independent and has been successfully applied to analysis of diverse materials including basalts, meteorites, komatiites, kimberlites and carbonatites. The relative simplicity of this technique, coupled with the ease of digestion (and samplespike equilibration) of large difficult-to-dissolve samples, and the speed (2 days) with which samples can be digested and processed through the chemical separation scheme makes it an attractive new method for preparing samples for Lu-Hf isotopic investigation.

AB - A new digestion procedure and chemical separation technique has been developed for measurement of Lu/Hf and Hf isotope ratios that does not require high-pressure bombs or use of HF or HClO acids. Samples are digested in dilute HCl or HNO after flux-fusion at 1100 °C in the presence of lithium metaborate. High field strength elements (HFSE) and rare earth elements (REE) are separated from this solution by co-precipitation with iron hydroxide. The dissolved precipitate (in 2 mol l HCl) is loaded directly onto a standard cation exchange column which separates remaining sample matrix from the heavy REE (Lu+Yb), and the middle-light REE and HFSE (Hf). The middle-light REE and individual HFSE are then separated (10.5, 9 and 6 mol l HCl) using a miniaturized column containing TEVA spec resin which provides a REE-, Ti- and Zr-free Hf cut. This chemical separation scheme can also be readily adapted for isotopic analysis of the Sm-Nd system and/or the other HFSE (Ti, Zr). Total procedural blanks for this technique are <100 pg and <2 pg for Hf and Lu, respectively, even when digesting large (0.5 g) samples. We present data from replicate digestions of international rock reference materials which demonstrate this technique routinely reproduces Lu/Hf ratios to <0.2% (2s) and 176Hf/177Hf isotope ratios to <30 ppm (2s). Moreover, the technique is matrix-independent and has been successfully applied to analysis of diverse materials including basalts, meteorites, komatiites, kimberlites and carbonatites. The relative simplicity of this technique, coupled with the ease of digestion (and samplespike equilibration) of large difficult-to-dissolve samples, and the speed (2 days) with which samples can be digested and processed through the chemical separation scheme makes it an attractive new method for preparing samples for Lu-Hf isotopic investigation.

UR - http://www.scopus.com/inward/record.url?scp=1942427361&partnerID=8YFLogxK

U2 - 10.1111/j.1751-908X.2003.tb00641.x

DO - 10.1111/j.1751-908X.2003.tb00641.x

M3 - Journal article

AN - SCOPUS:1942427361

VL - 27

SP - 133

EP - 145

JO - Geostandards and Geoanalytical Research

JF - Geostandards and Geoanalytical Research

SN - 1639-4488

IS - 2

ER -