The correlation between molecular structure and tendency to maintain or to destroy iron passivity in aqueous solutions—i. The electrostatic hypothesis
The electrostatic hypothesis of Cartledge relates the internal charge distribution of anions of the form XO 4 n− to their ability to maintain or to destroy passivity. Application of the hypothesis to other species is considered here. Certain soluble compounds, e.g. carboxylic acid salts, appear to c...
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Veröffentlicht in: | Corrosion science 1979, Vol.19 (2), p.123-130 |
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creator | Rostron, A.J. |
description | The electrostatic hypothesis of Cartledge relates the internal charge distribution of anions of the form XO
4
n−
to their ability to maintain or to destroy passivity. Application of the hypothesis to other species is considered here.
Certain soluble compounds, e.g. carboxylic acid salts, appear to conform. However there are some contradictions. Some of these are explained by hydrogen bonding, as with fluorine-containing compounds. With certain nitrogen-containing passivity stabilisers, in order to fit their behaviour to the hypothesis, rearrangement of an electron lone pair is postulated to occur when the compound adsorbs at the passive surface. |
doi_str_mv | 10.1016/0010-938X(79)90045-3 |
format | Article |
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4
n−
to their ability to maintain or to destroy passivity. Application of the hypothesis to other species is considered here.
Certain soluble compounds, e.g. carboxylic acid salts, appear to conform. However there are some contradictions. Some of these are explained by hydrogen bonding, as with fluorine-containing compounds. With certain nitrogen-containing passivity stabilisers, in order to fit their behaviour to the hypothesis, rearrangement of an electron lone pair is postulated to occur when the compound adsorbs at the passive surface.</description><identifier>ISSN: 0010-938X</identifier><identifier>EISSN: 1879-0496</identifier><identifier>DOI: 10.1016/0010-938X(79)90045-3</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><ispartof>Corrosion science, 1979, Vol.19 (2), p.123-130</ispartof><rights>1979</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c250t-23c9964e1006e5d09307b4746690c603657b1e8e0b5056ee748b0d96aa7ab0293</citedby><cites>FETCH-LOGICAL-c250t-23c9964e1006e5d09307b4746690c603657b1e8e0b5056ee748b0d96aa7ab0293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0010938X79900453$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Rostron, A.J.</creatorcontrib><title>The correlation between molecular structure and tendency to maintain or to destroy iron passivity in aqueous solutions—i. The electrostatic hypothesis</title><title>Corrosion science</title><description>The electrostatic hypothesis of Cartledge relates the internal charge distribution of anions of the form XO
4
n−
to their ability to maintain or to destroy passivity. Application of the hypothesis to other species is considered here.
Certain soluble compounds, e.g. carboxylic acid salts, appear to conform. However there are some contradictions. Some of these are explained by hydrogen bonding, as with fluorine-containing compounds. With certain nitrogen-containing passivity stabilisers, in order to fit their behaviour to the hypothesis, rearrangement of an electron lone pair is postulated to occur when the compound adsorbs at the passive surface.</description><issn>0010-938X</issn><issn>1879-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><recordid>eNp9UU1LAzEQDaJgrf4DDzmJHrbOfiWbiyDFLyh4qeAtZLNTGtluapKt9OaP8ODv85eYteLRQwgzvDfvzRtCTlOYpJCyS4AUEpFXz-dcXAiAokzyPTJKKy4SKATbJ6M_yCE58v4FALLYGZHP-RKpts5hq4KxHa0xvCF2dGVb1H2rHPXB9Tr0DqnqGhqwa7DTWxosXSnThfiodUPZYITaLTUuzlkr783GhFh2VL32aHtPvW37QcV_vX-YCR20McpElg9RXtPldm3DEr3xx-RgoVqPJ7__mDzd3syn98ns8e5hej1LdFZCSLJcC8EKTAEYlg2IHHhd8IIxAZpBzkpep1gh1CWUDJEXVQ2NYEpxVUMm8jE5281dOxtd-iBXxmtsW9UNlmWWM2BVySOw2AF1dOsdLuTamZVyW5mCHM4gh4zlkLHkQv6cQeaRdrWjYVxiY9BJr00MEBvj4uayseb_Ad9vOpPQ</recordid><startdate>1979</startdate><enddate>1979</enddate><creator>Rostron, A.J.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>1979</creationdate><title>The correlation between molecular structure and tendency to maintain or to destroy iron passivity in aqueous solutions—i. The electrostatic hypothesis</title><author>Rostron, A.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c250t-23c9964e1006e5d09307b4746690c603657b1e8e0b5056ee748b0d96aa7ab0293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rostron, A.J.</creatorcontrib><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Corrosion science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rostron, A.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The correlation between molecular structure and tendency to maintain or to destroy iron passivity in aqueous solutions—i. The electrostatic hypothesis</atitle><jtitle>Corrosion science</jtitle><date>1979</date><risdate>1979</risdate><volume>19</volume><issue>2</issue><spage>123</spage><epage>130</epage><pages>123-130</pages><issn>0010-938X</issn><eissn>1879-0496</eissn><abstract>The electrostatic hypothesis of Cartledge relates the internal charge distribution of anions of the form XO
4
n−
to their ability to maintain or to destroy passivity. Application of the hypothesis to other species is considered here.
Certain soluble compounds, e.g. carboxylic acid salts, appear to conform. However there are some contradictions. Some of these are explained by hydrogen bonding, as with fluorine-containing compounds. With certain nitrogen-containing passivity stabilisers, in order to fit their behaviour to the hypothesis, rearrangement of an electron lone pair is postulated to occur when the compound adsorbs at the passive surface.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/0010-938X(79)90045-3</doi><tpages>8</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals |
title | The correlation between molecular structure and tendency to maintain or to destroy iron passivity in aqueous solutions—i. The electrostatic hypothesis |
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