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11. |
Preconcentration and Spectrophotometric Determination of Chromium (VI) and Total Chromium in Drinking Water by the Sorption of Chromium Diphenylcarbazone with Surfactant Coated Alumina |
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Analytical Letters,
Volume 29,
Issue 11,
1996,
Page 2007-2014
JamshidL. Manzoori*,
MohammadH. Sorouraddin,
Farzaneh Shemiran,
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摘要:
A simple and inexpensive method for determining chromium (VI) in drinking water by spectrophotometry after preconcentration with sodium dodecyl sulphate (SDS) coated alumina column is described. Chromium(VI) is reacted with diphenylcarbazide (DPC) and the Cr-DPC complex is quantitatively adsorbed onto a SDS coated alumina column from 800 ml of sample solution. The complex is then eluted with a 8 ml mixture of methanol, acetone and hydrochloric acid and determined by spectrophotometry. Total chromium can be determined after oxidation of chromium (III) to chromium (VI) by KMnO4. The relative standard deviation (10 replicate analyses) at the 10 μg l−1of chromium (VI) and 10 μg l−1of total chromium were 3.5% and 3.4% and corresponding limits of detection (based on 3 σ) were 0.040 μg l−1and 0.033 μg l−1, respectively.
ISSN:0003-2719
DOI:10.1080/00032719608000807
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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12. |
Kinetic Flow Injection Spectrophotometric Determination of Nitrite by its Catalytic Effect on the Oxidation of Chlorophosphonazo-pN by Bromate |
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Analytical Letters,
Volume 29,
Issue 11,
1996,
Page 2015-2023
Chen Xingguo,
Wang Ketai,
Hu Zhide,
Zhao Zhengfeng,
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PDF (283KB)
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摘要:
A flow injection kinetic method has been developed for the determination of nitrite, based on its catalytic effect on bromate oxidation of chlorophosphonazo-pN in H2SO4medium. The reaction is followed spectrophotometrically by measuring the decrease in the absorbance at 551 nm. The sampling frequency was 83 h−1. The calibration curve was linear between 0.050 and 1.00 μg/ml, and the detection limit was 0.018 μg/ml. The proposed method was applied to the determination of nitrite in waters and soil with satisfactory results.
ISSN:0003-2719
DOI:10.1080/00032719608000808
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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13. |
Separation and Determination of D-Gluconic Acid Produced During Fermentation by Capillary Zone Electrophoresis |
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Analytical Letters,
Volume 29,
Issue 11,
1996,
Page 2025-2037
ZiPing Zhang,
ZhiDe Hu*,
GengLiang Yang,
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PDF (363KB)
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摘要:
A novel method was developed for separation and determination of D-gluconic acid produced during fermentation by capillary zone electrophoresis (CZE) with direct UV detection at 214 nm, using selected carrier electrolyte composed of 6 mM potassium biphthalate, 50 mM disodium hydrogen phosphate and 15% (v/v) acetonitrile. The effects of concentration of phthalate, phosphate and organic modifier (acetonitrile), as well as temperature for the separation were investigated. The method is simple, inexpensive and will make it very useful in the gluconic acid industry.
ISSN:0003-2719
DOI:10.1080/00032719608000809
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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14. |
The H-Point Standard Additions Method When the Matrix Effect is Absent. Application to the Determination of Certain Cephalosporins and their Acid-Induced Degradation Products |
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Analytical Letters,
Volume 29,
Issue 11,
1996,
Page 2039-2054
Pilar Campíns-Falcó,
Luisa Gallo-Martínez,
Adela Sevillano-Cabeza,
Francisco Bosch-Reig,
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PDF (525KB)
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摘要:
This paper discusses the requirements and scope of application of the H-point Standard Additions Method (HPSAM) when the matrix effect is absent. It is demonstrated that the HPSAM calibration method works well with slopes of calibration graphs as standards. It is applied to the resolution of binary mixtures of intact and acid degraded cephalosporins. The results obtained are better than those obtained by second derivative spectrophotometry.
ISSN:0003-2719
DOI:10.1080/00032719608000810
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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15. |
Resolution of Overlapping Bands – An Idea for Quantitative Analysis of Undefined Mixturesa |
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Analytical Letters,
Volume 29,
Issue 11,
1996,
Page 2055-2069
Liudmil Antonov,
Daniela Nedeltcheva,
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PDF (438KB)
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摘要:
A method for quantitative analysis of multicomponent mixtures with unknown individual spectra of the components, based on resolution of overlapping bands, is developed and its reliability is illustrated in analysis of both model and real mixtures. The two-step optimization procedure allows attainment of high precision, the molar parts and the individual spectra of the components. This approach could be used in molecular spectroscopy (UV-Vis-NIR, IR, Raman and CD spectroscopy) as well as in chromatography.
ISSN:0003-2719
DOI:10.1080/00032719608000811
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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16. |
List of Contributors |
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Analytical Letters,
Volume 29,
Issue 11,
1996,
Page -
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PDF (26KB)
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ISSN:0003-2719
DOI:10.1080/00032719608000814
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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