University of North Florida
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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

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Li-Ching Tian

Abbrev:
Tian, L.C.
Other Names:
Address:
Department of Chemistry, Nanjing University, Nanjing, 210 093, China
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Citations 2

"Sequential Determination Of Tin, Arsenic, Bismuth And Antimony In Marine Sediment Material By Inductively Coupled Plasma Atomic Emission Spectrometry Using A Small Concentric Hydride Generator And L-cysteine As Prereductant"
Fresenius J. Anal. Chem. 1998 Volume 361, Issue 2 Pages 155-157
Y.-L. Feng A, H.-Y. Chen A, H.-W. Chen A, Li-Ching Tian

Abstract: A hydride generation system using a small concentric hydride generator combined with inductively coupled plasma atomic emission spectrometry (ICP-AES) was established to determine tin, arsenic, bismuth and antimony in a marine sediment material with L-cysteine as a pre-reductant. Influences of concentrations of three kinds of acids (HCl, HNO3 and HClO4), L-cysteine, and sodium tetrahydroborate(III) as well as sodium hydroxide were investigated. The interferences from transition ions were found to be insignificant for determination of the four elements in presence of L-cysteine. Under optimized conditions the detection limits were 0.6 ng/mL for arsenic(III), 0.8 ng/mL for antimony(III), 1.7 ng/mL for tin(IV), and 1.2 ng/mL for bismuth(III). The method was applied to determine the four elements in standard marine sediment materials and the results were in agreement with certified values.
Tin Arsenic Bismuth Antimony Marine Mass spectrometry Phase separator Volatile generation Apparatus

"Determination Of Chemical Oxygen Demand In Aqueous Environmental Samples By Segmented Flow Injection Analysis"
Anal. Chim. Acta 1992 Volume 261, Issue 1-2 Pages 301-305
Li-Ching Tian* and Sao-Ming Wu

Abstract: A method is described for the determination of chemical oxygen demand (C.O.D) in aqueous environmental samples by segmented flow injection analysis. KMnO4 solution used as both an oxidant and a spectrophotometric reagent and D-glucose as a standard. When the reaction temperature is 95°C, the residence time is about 8 min and a sample throughput of 80/h can be achieved. The detection limit and relative standard deviation are 2 mg/litre and 0.7%, respectively, and the recovery is 85-95%. Chloride ion up to levels of 1500 mg/litre does not interfere with the results. C.O.D compared with those obtained using the Japanese Industrial Standard method and agreed within an error range of ±10%.
Chemical oxygen demand Environmental Spectrophotometry Interferences Method comparison Standard method Heated reaction