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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>8</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1997</Year>
					<Month>09</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>ELECTROCHEMICAL BEHAVIOUR OF U(V1)
NITRATE IN CHLOROFORM AT A MERCURY
ELECTRODE
THE DEPENDENCE ON SUPPORTING
ELECTROLYTE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31250</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>The mechanistic aspects of the electrochemical reduction of U(V1) nitrate at a
mercury electrode in chloroform, using three different supporting electrolytes, are
described. In the presence of tetrabutylarnmonium perchlorate (TBAP) as a neutral
electrolyte, UO  (NO )  , reduced in two irreversible electrochemical steps to form a U(V1)-U(V) binuclear complex and U(IV), respectively. In the presence of 0.75 M
piperidinium perchlorate (PP) + 0.25 M piperidine (P) as supporting electrolyte, the
reduction of U0  ( NO   )   occurred according to a one-electron irreversible process to U (V). The same behaviour was observed in the presence of 0.5 M tributylamrnonium perchlorate + 0.3 M tributylamine. The diffusion coefficients of U(VI) and U(VI)- U(V) binuclear complex determined by chronoamperometric measurement are 8.8 cm s  and  5.37 10  cm  s   respectively</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31250_7cc785bf3d68a7840ea16c08b2863213.pdf</ArchiveCopySource>
</Article>
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