University of North Florida
Browse the Citations
-OR-

Contact Info

Stuart Chalk, Ph.D.
Department of Chemistry
University of North Florida
Phone: 1-904-620-1938
Fax: 1-904-620-3535
Email: schalk@unf.edu
Website: @unf

View Stuart Chalk's profile on LinkedIn

Mohammad B. Shabani

Abbrev:
Shabani, M.B.
Other Names:
Address:
Department of Chemistry, Faculty of Science, The University of Tokyo, Hongo 113, Tokyo, Japan
Phone:
NA
Fax:
NA
Email:

Citations 2

"Sample Introduction By Online Two-stage Solvent Extraction And Back-extraction To Eliminate Matrix Interference And To Enhance Sensitivity In The Determination Of Rare-earth Elements With Inductively Coupled Plasma Mass Spectrometry"
Anal. Chem. 1991 Volume 63, Issue 19 Pages 2099-2105
Mohammad B. Shabani and Akimasa Masuda

Abstract: The described system contained a Gilson eight-channel peristaltic liquid delivery pump and Viton and Tygon tubes for feeding the organic and aqueous solution, respectively, while the extraction and back-extraction, respectively, were performed in 1- and 2-m Teflon coils each with a segmentor at the inlet and a sandwich-type Teflon phase separator (Sanuki Kogyo Co. Ltd., Tokyo, Japan) at the outlet and Teflon connecting tubes. The rare-earth elements were extracted from the sample solution (2 mL min-1) into a 0.1 M solution of bis-(2-ethylhexyl) hydrogen phosphate - 2-ethylhexyl dihydrogen phosphate (13:7) in hexane (0.6 mL min-1). The ensuing separated organic phase was mixed with octyl alcohol - heptane (1:1; 0.6 mL min-1) and then back-extracted with aqueous 2 M HNO3 containing 50 ng mL-1 of Cd as internal standard (0.4 mL min-1). The separated aqueous phase was then analyzed in a VG PlasmaQuad instrument with a Jarrell - Ash nebulizer (conditions detailed). The method was applied to synthetic sea water samples (enrichment factor 10; detection limits ranging from 0.16 pg g-1 of Tb, Ho or Lu to 1.2 pg g-1 of Nd) and to JG1a and JB1 standard rock and Jilin chondrite rock samples giving results which agreed with those obtained previously (procedures detailed).
Metals, rare earth Uranium Yttrium Mass spectrometry Spectrophotometry Spectrophotometry Sample preparation Interferences Preconcentration Sensitivity Solvent extraction

"Determination Of Trace Rhenium In Seawater By Inductively Coupled Plasma Mass Spectrometry With Online Preconcentration"
Anal. Chim. Acta 1992 Volume 261, Issue 1-2 Pages 315-321
Mohammad B. Shabani* and Akimasa Masuda

Abstract: An online column pre-concentration method is described for the determination of Re in seawater by inductively coupled plasma mass spectrometry. Minicolumns of 2 sizes (7 mm x 2 mm i.d. and 14 mm x 2 mm i.d.) containing the anion-exchange resin Dowex 1-X8 were used for the quant. pre-concentration of Re in seawater. The concentrated Re was eluted from the column with HNO3. A simple calibration technique with Lu as internal standard and also isotope dilution were used for the determination of Re in seawater. Enrichment factors of 38- or 101-fold were obtained using 10- or 50 mL seawater samples, respectively., and the relative standard deviations for replicate measurements (n = 3) were 2.62% for natural seawater and 0.34% for synthetic seawater. The detection limits after online pre-concentration of 10 and 50 mL of seawater were 0.27 and 0.1 pg/mL, respectively. Almost no contamination blank signal or matrix interferences were observed
Rhenium Sea Mass spectrometry Preconcentration Interferences Dowex