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				<datestamp>2013-12-31T06:16:57Z</datestamp>
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	<dc:title xml:lang="en-US">Kinetics and mechanism of oxidation of amido black by sodium  N-halo-p-toluenesulfonamides in acidic medium: Spectrophotometric approach</dc:title>
	<dc:creator>Shubha, Jayachamarajapura Pranesh</dc:creator>
	<dc:creator>Vinutha, Kotabagi</dc:creator>
	<dc:creator>Puttaswamy, Puttaswamy</dc:creator>
	<dc:subject xml:lang="en-US">Azo dye</dc:subject>
	<dc:subject xml:lang="en-US">Amido black</dc:subject>
	<dc:subject xml:lang="en-US">Chloramine-T</dc:subject>
	<dc:subject xml:lang="en-US">Bromamine-T</dc:subject>
	<dc:subject xml:lang="en-US">Acidic medium</dc:subject>
	<dc:subject xml:lang="en-US">Oxidation kinetics</dc:subject>
	<dc:description xml:lang="en-US">The kinetics of oxidative decolorization of amido black (AB, Naphthol blue black) by chloramine-T (CAT) and bromamine-T (BAT) in acidic medium has been investigated spectrophotometrically (λmax = 618 nm) at 298 K. Kinetic runs were performed under pseudo first-order conditions of [Oxidant]o &gt;&gt; [AB]o. Under identical experimental conditions, reactions with both the oxidants follow identical kinetics with a first-order dependence on each [Oxidant]o and [AB] and a fractional-order dependence on [HClO4]. Stoichiometry of the reaction was found to be 1:4 and the oxidation products were identified. The reaction was studied at different temperatures and various activation parameters have been computed. Effects of p-toluenesulfonamide, halide ions, ionic strength and dielectric constant of the medium have been investigated. Reaction mixture fails to induce polymerization of acrylonitrile. The rate of oxidation of AB is about three-fold faster with BAT as compared to CAT. This may be attributed to the difference in electrophilicity of Cl+ and Br+ ions and also the Vander Waals radii of chlorine and bromine. Plausible mechanism and related rate law have been deliberated for the observed kinetics.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2013-12-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/806</dc:identifier>
	<dc:identifier>10.5155/eurjchem.4.4.408-413.806</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 4 No. 4 (2013): December 2013; 408-413</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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