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胡斌, Lei Wang, Bin Hu, *, Shengqing Li and Zucheng Jiang
J. Anal. At. Spectrom., 2001, 16, 847-851,-0001,():
-1年11月30日
An in-situ electrothermal fluorination-assisted matrix removal method was developed with PTFE as chemical modifier, and trace-levels of Cr, Co and V in ZrO2 powder were determined. The solid samples were directly introduced into the graphite furnace in the form of a slurry, where the Zr matrix reacted with the active carbon fluoride formed by electrothermal decomposition of PTFE during the pyrolysis stage. Without loss of analytes, the Zr matrix was completely vaporized and removed by the carrier gas. As a result, the matrix interference, which was serious without the modifier, was effectively suppressed, and the chemical attack of the excess of the Zr matrix on the graphite tube was also minimized. The standard additions calibration and the aqueous standard calibration were compared and similar results were obtained. The removal of matrix, the background absorption, the chemical modification of PTFE and the temperature-time program of the graphite furnace were investigated and optimized. The proposed method was applied to the direct determination of trace amounts of Cr, Co and V in ZrO2 powder with aqueous calibration and the results obtained were in good agreement with those obtained by pneumatic nebulization ICP-AES after digestion and separation of the matrix Zr with PMBP extraction. The detection limits of Cr, Co and V were 0.20, 0.32 and 3.7mg g21, respectively.
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胡斌, Zhefeng Fan, Bin Hu*, Zucheng Jiang
Spectrochimica Acta Part B 60 (2005) 65-71,-0001,():
-1年11月30日
A sensitive and simple method for low temperature electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP-OES) determination of V (Ⅳ) and V (Ⅴ) after separation/preconcentration by a micro-column packed with immobilized thenoyltrifluoroacetone (TTA) on microcrystalline naphthalene has been developed. Thenoyltrifluoroacetone was used as both a chelating agent for micro-column separation/preconcentration and a chemical modifier for ETV-ICP-OES determination of vanadium. Both vanadium species could be trapped by micro-column at pH 4.0, and the vanadate (VO2+) ion could be collected selectively at pH 2.4. Solid material loaded with analyte in the micro-column was dissolved with 100 AL of acetone containing 2.0 mmol L1 TTA and the vanadium was determined subsequently by ETV-ICP-OES. The concentration of vanadyl (VO2+) ion was calculated by subtracting the vanadate concentration from the total concentration of vanadium. Under the optimized experimental conditions, the detection limit (3r) for the preconcentration of 5mL of aqueous solution is 0.068 Ag L1 for both species and the relative standard deviations were 4.3% for vanadium (Ⅴ) and 4.8% for vanadium (Ⅵ) (c=10 Ag L1, n=7), respectively. The method was applied successfully to the determination of vanadium (Ⅳ) and vanadium (Ⅴ) in natural water samples.
Vanadium speciation, Microcrystalline naphthalene, Thenoyltrifluoroacetone, ETV-ICP-OES
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胡斌, Shuai Qin, Hu Bin, *, Qin Yongchao, Ruth Wanjau and Jiang Zucheng
J. Anal. At. Spectrom., 2000, 15, 1413-1416,-0001,():
-1年11月30日
A method is proposed to determine trace rare earth impurities in high-purity CeO2 by HPLC combined with electrothermal vaporization inductively coupled plasma atomic emission spectrometry (ETV-ICP-AES). The chromatographic retention behaviours of the matrix (Ce) and rare earth impurities were studied using 2-ethylhexyl hydrogen 2-ethylhexylphosphonate (P507) resin as the stationary phase and dilute nitric acid as the mobile phase. It was found that the matrix (Ce) can be separated quantitatively with dilute nitric acid as the mobile phase, and the rare earth impurities (Pr
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胡斌, Bing Cai, Bin Hu*, Hongchun Xiong, Zhenhuan Liao, Lesen Mao, Zucheng Jiang
Talanta 55 (2001) 85-91,-0001,():
-1年11月30日
A sensitive and rapid method for the determination of lanthanum, europium and ytterbium by inductively coupled plasma atomic emission spectrometry (ICP-AES) after solid-liquid extraction with microcrystalline naphthalene was developed. Analytes could be quantitatively adsorbed on tribromoarsenazo-cetylpyridinium bromide-naphthalene (TBA-CPB-naphthalene) packed in a column and determined by ICP-AES after desorption with 3mol l−1 HCl. The effect of various experimental parameters, such as pH, reagent amounts, naphthalene concentrations and diverse ions, on the determination of interesting elements were investigated in detail. Under the optimized experimental conditions, the detection limits of this method for La3+, Eu3+ and Yb3+ were 1.3-8.6ng ml−1, and the relative standard deviations obtained for nine replicate determinations at a concentration of 0.5gml−1 were 1.4-2.2%. The proposed method has been applied in the analysis of NIES CRM No.8 vehicle exhaust particulates and GBW 07602 GSV-1 bush branches and leaves for La, Eu and Yb, and La in NIST SRM 1752 citrus leaves samples; the analytical results were in good agreement with reference values.
Microcrystalline naphthalene, Lanthanum, europium and ytterbium, Tribromoarsenazo, Inductively coupled plasma atomic emission spectrometry, Environmental and biological samples
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胡斌, Linbo Xia, Bin Hu, *, Zucheng Jiang, Yunli Wu, and Yu Liang'
Analytical Chemistry, Vol. 76, No.10, May 15, 2004,-0001,():
-1年11月30日
A new method of single-drop microextraction combined with low-temperature electrothermal vaporization (LTETV)-ICPMS was proposed for the determination of trace Be, Co, Pd, and Cd with benzoylacetone (BZA) as both extractant and chemical modifier. Several factors that influence the microextraction efficiency, such as sample flow rate, microdrop volume, and extraction time, were investigated and the optimized microextraction conditions were established. Be, Co, Pd, and Cd in the postextraction organic phase were directly determined by LTETV-ICPMS with the use of BZA as chemical modifier. The chemical modification of BZA in LTETV-ICPMS was studied, and the factors affecting the formation of chelates and vaporization/ transportation of chelates were investigated. Under the optimized conditions, the detection limits of the method were 0.12, 0.99, 1.5, and 0.27pg/mL for Be, Co, Pd, and Cd, and the relative standard deviations for 0.1ng/mL Be, Co, Pd, and Cd were 16, 14, 14, and 11%, respectively. After 10min of extraction, the enrichment factors were 160 (Be), 125 (Co), 40 (Pd), and 180 (Cd). The proposed method was applied to the determination of trace Be, Co, Pd, and Cd in biological reference materials, and the determined values were in good greement with the certified values.
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