1983
DOI: 10.5271/sjweh.2384
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Sampling and analysis of hexavalent chromium during exposure to chromic acid mist and welding fumes.

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Cited by 14 publications
(16 citation statements)
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“…The diphenylcarbazide (DPC) complexing reagent was prepared by dissolving 0.25 g of DPC in 50 ml of acetone in a 100 ml volumetric flask and adding water to volume. 4 Standards for determination of total chromium were prepared from a commercial atomic absorption spectrometry (AAS) standard solution (Cr 1.000 g ml 21 , BDH, Poole, Dorset, UK). Standards of hexavalent chromium were diluted from a stock solution (1.000 g ml 21 ) made by dissolving potassium dichromate in water.…”
Section: Chemicalsmentioning
confidence: 99%
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“…The diphenylcarbazide (DPC) complexing reagent was prepared by dissolving 0.25 g of DPC in 50 ml of acetone in a 100 ml volumetric flask and adding water to volume. 4 Standards for determination of total chromium were prepared from a commercial atomic absorption spectrometry (AAS) standard solution (Cr 1.000 g ml 21 , BDH, Poole, Dorset, UK). Standards of hexavalent chromium were diluted from a stock solution (1.000 g ml 21 ) made by dissolving potassium dichromate in water.…”
Section: Chemicalsmentioning
confidence: 99%
“…Hexavalent chromium was determined using spectrophotometry after DPC complexation. 4 A 2 ml aliquot was withdrawn from each sample and transferred to a 15 ml calibrated flask. Complexing reagent (1 ml), 0.5 m sulfuric acid (5 ml) and water to volume were added and the sample was left to stand for 10 min to allow formation of the complex.…”
Section: Determination Of Chromium In Tanned Leathermentioning
confidence: 99%
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“…If Cr(VI) seems to be quantitatively extracted without degradation for C1 and C3, its extraction with ammonium/ammonia buffer solution is accompanied with its reduction for C2 and C4. The literature reveals that an alkaline medium allows the stabilisation of Cr(VI) by decreasing its oxidant power and no reduction was observed in presence of metals such as Fe(II), Mn(II), or Ni(II) [14,15]. However, the buffer solution used has a high ionic strength that allows a good stripping of the coating but, unfortunately, potentially oxidizable compounds can also be extracted.…”
Section: Optimisation Of Cr(vi) Extraction From Coatingsmentioning
confidence: 93%
“…Cr(VI) being a strong oxidant in acid solution, it is recommended to use slightly acid or alkaline solutions to stabilise it during extraction. However, for pH between 4 and 5, Cr(VI) reduction into Cr(III) was evidenced [14,15]. Thus, it seems preferable to use more alkaline solutions such as phosphate buffer (pH 8) [16,17,18,19], ammonium/ammonia buffer (8<pH<9) [19,20,21,22], alkaline digestion with a carbonate/sodium hydroxide mixture (pH 12) [23,24,25,26,27], or sodium hydroxide at pH 13 [20,26].…”
Section: Hexavalent Chromium Extraction From Coatingsmentioning
confidence: 98%