In situ monitoring of crevice corrosion morphology of Type 316L stainless steel and repassivation behavior induced by sulfate ions
•Repassivation of crevice corrosion on Type 316L was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4.•The active dissolution of Type 316L stainless steel in 1M NaCl at pH 0.4 was slightly suppressed by SO42− ions in anodic polarization measurements.•The...
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Veröffentlicht in: | Corrosion science 2017-10, Vol.127, p.131-140 |
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creator | Aoyama, Takahito Sugawara, Yu Muto, Izumi Hara, Nobuyoshi |
description | •Repassivation of crevice corrosion on Type 316L was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4.•The active dissolution of Type 316L stainless steel in 1M NaCl at pH 0.4 was slightly suppressed by SO42− ions in anodic polarization measurements.•The accumulation of SO42− ions toward the crevice brought about the repassivation.
To analyze the repassivation mechanism induced by SO42− ions, in situ monitoring of the crevice corrosion morphology on Type 316L stainless steel was performed. The repassivation of the crevice corrosion was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4. The active dissolution of Type 316L stainless steel was suppressed by SO42− ions at pH 0.4 in anodic polarization measurements. The transition from active to passive states inside the crevice was likely promoted by SO42− ions. |
doi_str_mv | 10.1016/j.corsci.2017.08.005 |
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To analyze the repassivation mechanism induced by SO42− ions, in situ monitoring of the crevice corrosion morphology on Type 316L stainless steel was performed. The repassivation of the crevice corrosion was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4. The active dissolution of Type 316L stainless steel was suppressed by SO42− ions at pH 0.4 in anodic polarization measurements. The transition from active to passive states inside the crevice was likely promoted by SO42− ions.</description><identifier>ISSN: 0010-938X</identifier><identifier>EISSN: 1879-0496</identifier><identifier>DOI: 10.1016/j.corsci.2017.08.005</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Anodic polarization ; Austenitic stainless steels ; Corrosion ; Corrosion mechanisms ; Crevice corrosion ; Monitoring ; Potentiostatic ; Repassivation ; Stainless steel</subject><ispartof>Corrosion science, 2017-10, Vol.127, p.131-140</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright Elsevier BV Oct 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-7029f1da87cf96b1efa7d500e7b4f3d9c70aec701add7603bc7b0a3caf200823</citedby><cites>FETCH-LOGICAL-c400t-7029f1da87cf96b1efa7d500e7b4f3d9c70aec701add7603bc7b0a3caf200823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.corsci.2017.08.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids></links><search><creatorcontrib>Aoyama, Takahito</creatorcontrib><creatorcontrib>Sugawara, Yu</creatorcontrib><creatorcontrib>Muto, Izumi</creatorcontrib><creatorcontrib>Hara, Nobuyoshi</creatorcontrib><title>In situ monitoring of crevice corrosion morphology of Type 316L stainless steel and repassivation behavior induced by sulfate ions</title><title>Corrosion science</title><description>•Repassivation of crevice corrosion on Type 316L was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4.•The active dissolution of Type 316L stainless steel in 1M NaCl at pH 0.4 was slightly suppressed by SO42− ions in anodic polarization measurements.•The accumulation of SO42− ions toward the crevice brought about the repassivation.
To analyze the repassivation mechanism induced by SO42− ions, in situ monitoring of the crevice corrosion morphology on Type 316L stainless steel was performed. The repassivation of the crevice corrosion was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4. The active dissolution of Type 316L stainless steel was suppressed by SO42− ions at pH 0.4 in anodic polarization measurements. The transition from active to passive states inside the crevice was likely promoted by SO42− ions.</description><subject>Anodic polarization</subject><subject>Austenitic stainless steels</subject><subject>Corrosion</subject><subject>Corrosion mechanisms</subject><subject>Crevice corrosion</subject><subject>Monitoring</subject><subject>Potentiostatic</subject><subject>Repassivation</subject><subject>Stainless steel</subject><issn>0010-938X</issn><issn>1879-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9UE1LxDAQDaLguvoPPAQ8t062tWkugogfCwte9uAtpMlEs9SkJm1hr_5ys6xnLzMD72N4j5BrBiUD1tzuSh1i0q5cAeMltCXA3QlZsJaLAmrRnJIFAINCVO37OblIaQcAmQsL8rP2NLlxol_BuzFE5z9osFRHnJ1Gmn1jSC74jMfhM_ThY3_At_sBacWaDU2jcr7HlPKF2FPlDY04qJTcrMaDssNPNbsQqfNm0mhot6dp6q0akWY8XZIzq_qEV397SbbPT9vH12Lz9rJ-fNgUugYYCw4rYZlRLddWNB1Dq7i5A0De1bYyQnNQmAdTxvAGqk7zDlSllV0BtKtqSW6OtkMM3xOmUe7CFH3-KJlomkpwAXVm1UeWzrlTRCuH6L5U3EsG8lC23Mlj2fJQtoRW5rKz7P4owxxgdhhlZqDPaV1EPUoT3P8Gvx7ujSY</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Aoyama, Takahito</creator><creator>Sugawara, Yu</creator><creator>Muto, Izumi</creator><creator>Hara, Nobuyoshi</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SE</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>201710</creationdate><title>In situ monitoring of crevice corrosion morphology of Type 316L stainless steel and repassivation behavior induced by sulfate ions</title><author>Aoyama, Takahito ; Sugawara, Yu ; Muto, Izumi ; Hara, Nobuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-7029f1da87cf96b1efa7d500e7b4f3d9c70aec701add7603bc7b0a3caf200823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Anodic polarization</topic><topic>Austenitic stainless steels</topic><topic>Corrosion</topic><topic>Corrosion mechanisms</topic><topic>Crevice corrosion</topic><topic>Monitoring</topic><topic>Potentiostatic</topic><topic>Repassivation</topic><topic>Stainless steel</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aoyama, Takahito</creatorcontrib><creatorcontrib>Sugawara, Yu</creatorcontrib><creatorcontrib>Muto, Izumi</creatorcontrib><creatorcontrib>Hara, Nobuyoshi</creatorcontrib><collection>CrossRef</collection><collection>Corrosion Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering 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>Aoyama, Takahito</au><au>Sugawara, Yu</au><au>Muto, Izumi</au><au>Hara, Nobuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ monitoring of crevice corrosion morphology of Type 316L stainless steel and repassivation behavior induced by sulfate ions</atitle><jtitle>Corrosion science</jtitle><date>2017-10</date><risdate>2017</risdate><volume>127</volume><spage>131</spage><epage>140</epage><pages>131-140</pages><issn>0010-938X</issn><eissn>1879-0496</eissn><abstract>•Repassivation of crevice corrosion on Type 316L was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4.•The active dissolution of Type 316L stainless steel in 1M NaCl at pH 0.4 was slightly suppressed by SO42− ions in anodic polarization measurements.•The accumulation of SO42− ions toward the crevice brought about the repassivation.
To analyze the repassivation mechanism induced by SO42− ions, in situ monitoring of the crevice corrosion morphology on Type 316L stainless steel was performed. The repassivation of the crevice corrosion was observed when the solution was changed from 1M NaCl to 0.88M Na2SO4 or to 1M NaCl-0.88M Na2SO4. The active dissolution of Type 316L stainless steel was suppressed by SO42− ions at pH 0.4 in anodic polarization measurements. The transition from active to passive states inside the crevice was likely promoted by SO42− ions.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.corsci.2017.08.005</doi><tpages>10</tpages></addata></record> |
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subjects | Anodic polarization Austenitic stainless steels Corrosion Corrosion mechanisms Crevice corrosion Monitoring Potentiostatic Repassivation Stainless steel |
title | In situ monitoring of crevice corrosion morphology of Type 316L stainless steel and repassivation behavior induced by sulfate ions |
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