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				<datestamp>2016-09-30T03:57:42Z</datestamp>
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	<dc:title xml:lang="en-US">Synthesis, characterization and thermal decomposition of 2’-amino-6’-(1H-indol-3-yl)-1-methyl-2-oxospiro-[indoline-3,4’-pyran]-3’,5’-dicarbonitrile under non-isothermal condition in nitrogen atmosphere</dc:title>
	<dc:creator>Nalini, Ganesan</dc:creator>
	<dc:creator>Jayachandramani, Natesan</dc:creator>
	<dc:creator>Suresh, Radhakrishnan</dc:creator>
	<dc:creator>Thanikachalam, Venugopal</dc:creator>
	<dc:creator>Manikandan, Govindasamy</dc:creator>
	<dc:subject xml:lang="en-US">Spirooxindole</dc:subject>
	<dc:subject xml:lang="en-US">Coats-Redfern method</dc:subject>
	<dc:subject xml:lang="en-US">Thermal decomposition</dc:subject>
	<dc:subject xml:lang="en-US">Flynn-Wall-Ozawa method</dc:subject>
	<dc:subject xml:lang="en-US">Thermodynamic parameters</dc:subject>
	<dc:subject xml:lang="en-US">Kissinger-Akahira-Sunose method</dc:subject>
	<dc:description xml:lang="en-US">The kinetics and decomposition of a new spirooxindole compound, 2’-amino-6’-(1H-indol-3-yl)-1-methyl-2-oxospiro[indoline-3,4’-pyran]-3’,5’-dicarbonitrile was studied by thermo gravimetric technique under non-isothermal conditions. The kinetic parameters were calculated using model-free (Friedman, Kissinger-Akahira-Sunose and Flynn-Wall-Ozawa methods) and model-fitting (Coats-Redfern) methods. The results of the Friedman isoconversional analysis of the thermo gravimetric data suggested that the investigated decomposition process follows a single-step.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2016-09-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/1442</dc:identifier>
	<dc:identifier>10.5155/eurjchem.7.3.380-386.1442</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 7 No. 3 (2016): September 2016; 380-386</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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