Topic
Potassium dichromate
About: Potassium dichromate is a research topic. Over the lifetime, 1430 publications have been published within this topic receiving 18967 citations. The topic is also known as: Potassium dichromate(VI) & Chromium potassium oxide.
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TL;DR: Two new uranyl coordination compounds, [C9H17N2]3[(UO2)2(CrO4)2Cl2(H2O)2]Cl·5H 2O (1) and [C 9H 17N 2]3 [UO 2)(C2O4]Cl] (2), have been synthesized by adding potassium dichromate (K2Cr2O7) or oxal...
Abstract: Two new uranyl coordination compounds, [C9H17N2]3[(UO2)2(CrO4)2Cl2(H2O)2]Cl·5H2O (1) and (C9H17N2)[(UO2)(C2O4)Cl] (2), have been synthesized by adding potassium dichromate (K2Cr2O7) or oxal...
3 citations
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TL;DR: In this article, the problems in the practical work are analyzed and the effective adjustment and control methods are adopted to reduce errors and to ensure reality of the determined water sample, which is the national standard method for determining COD in the industrial wastewater.
Abstract: The potassium dichromate method is the national standard method for determining COD in the industrial wastewater.Based on massive experiments,accuracy,recovery of the method,standard solution's stability and the sampling method are discussed in this paper.The problems in the practical work are analyzed.The effective adjustment and control methods are adopted to reduce errors and to ensure reality of the determined water sample.
3 citations
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TL;DR: In this paper, a study of the adsorption of 51Cr from aqueous solutions of labelled potassium dichromate on to coarse magnesium powder at room temperature was made.
Abstract: A study has been made of the adsorption of 51Cr, from aqueous solutions of labelled potassium dichromate, on to coarse magnesium powder at room temperature. The measurement of the rate of uptake of 51Cr on the powder and comparison with a magnesium standard of known area has led to a simple method for the determination of the surface area of the powder.
3 citations
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TL;DR: In this paper, the instability of 5-(1H-benzimidazol-2-yl)-hetarene-2 carboxylic acids was investigated.
Abstract: Oxidation of 5-(1-methyl-1H-benzimidazol-2-yl)thiophene-, and -selenophene-2-carbaldehydes with potassium dichromate in 20% aqueous sulfuric acid afforded the corresponding carboxylic acids. Analogous reaction with 5-(1-methyl-1H-benzimidazol-2-yl)furan-2-carbaldehyde led to the formation of 1-methyl-1H-benzimidazole as a result of decarboxylation of the primary oxidation product and subsequent decomposition of the furan ring. Probable factors responsible for instability of 5-(1H-benzimidazol-2-yl)-hetarene-2-carboxylic acids were considered. The oxidation of 2-furylnaphtho[2,3-d]- and 2-hetarylphenanthro-[9,10-d]imidazoles gave, respectively, an anthraquinone analog and 6,7-quinones. π-Electron-rich heterocycles in 2-furyl- and 2-pyrrolylphenanthro[9,10-d]imidazoles were oxidized completely, being replaced by hydrogen.
3 citations
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10 Aug 2000
TL;DR: In this article, a mixture of 0.0005-1 wt.% compound(s) selected from alkali iodides, manganese dioxide, lithium chloride, potassium dichromate, magnesium acetate, calcium chloride, barium nitrate, copper (II) chloride, copper(II) sulfate, iron chloride, cerium sulfates, vanadium sulfate and/or hydroquinone is applied to the hair and washed off after about 5-50 minutes.
Abstract: In oxidative coloring of human hair, composition A, with pH \} 9, contains oxidation dye precursor(s) (I) and metal salt(s) and/or hydroquinone is mixed, immediately before application, with a composition B, containing (I) and alkali to increase the pH \> 9 and with an acidic hydrogen peroxide composition, giving a mixture with pH 8-10.5; applied to the hair; and washed off after 5-50 minutes. In oxidative coloring of human hair, composition A contains oxidation dye precursor(s) (I) and 0.0005-1 wt.% compound(s) selected from alkali iodides, manganese dioxide, lithium chloride, potassium dichromate, magnesium acetate, calcium chloride, barium nitrate, copper (II) chloride, copper(II) sulfate, iron chloride, cerium sulfate, vanadium sulfate and/or hydroquinone. Immediately before application, composition A, with pH \} 9, is mixed with a composition B, containing (I) and enough alkali to increase the pH to over 9 and (then) with an acidic hydrogen peroxide composition, so that the mixture has pH 8-10.5. It is applied to the hair and washed off after about 5-50 minutes.
3 citations