Reagents for High Temperature Aqueous Chemistry: Trifluoromethanesulfonic Acid and its Salts
The rate of decomposition of trifluoromethanesulfonic acid (HTFMS) in water is first order with respect to each of H + and TFMS − . The bimolecular rate coefficient k H can be represented by at ionic strength 1.0 mol kg −1 over the temperature range 571 < T < 593 K, although the decomposition...
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Veröffentlicht in: | Canadian journal of chemistry 1975-10, Vol.53 (20), p.3053-3059 |
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creator | Fabes, Leonard Swaddle, Thomas Wilson |
description | The rate of decomposition of trifluoromethanesulfonic acid (HTFMS) in water is first order with respect to each of H
+
and TFMS
−
. The bimolecular rate coefficient k
H
can be represented by
at ionic strength 1.0 mol kg
−1
over the temperature range 571 < T < 593 K, although the decomposition occurs by two pathways of comparable importance, one leading to C(II) and S(VI) and the other to C(IV) and S(IV). In alkaline solution, the rate of decomposition of TFMS
−
is first order in each of TFMS
−
and OH
−
, and the bimolecular rate coefficients k
OH
at ionic strength 2.3 are given by
This represents a single reaction pathway leading initially to C(II) and S(VI) and ultimately to CO
3
2−
, SO
4
2−
, F
−
, and H
2
, since C(II) (as formate) reduces aqueous alkali to H
2
under the reaction conditions. No decomposition of NaTFMS could be detected after 24 h at 620 K in neutral aqueous solution. HTFMS reduces certain aqueous species at significant rates at moderate temperatures (e.g., Fe(III) to Fe(II) at 470 K), and metals which depend on oxide films for their corrosion resistance are attacked by HTFMS even at 294 K (e.g., Ti dissolves giving Ti(H
2
O)
6
3+
). Otherwise, HTFMS and its salts have good potentialities as inert electrolytes for aqueous studies at high temperatures. |
doi_str_mv | 10.1139/v75-433 |
format | Article |
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+
and TFMS
−
. The bimolecular rate coefficient k
H
can be represented by
at ionic strength 1.0 mol kg
−1
over the temperature range 571 < T < 593 K, although the decomposition occurs by two pathways of comparable importance, one leading to C(II) and S(VI) and the other to C(IV) and S(IV). In alkaline solution, the rate of decomposition of TFMS
−
is first order in each of TFMS
−
and OH
−
, and the bimolecular rate coefficients k
OH
at ionic strength 2.3 are given by
This represents a single reaction pathway leading initially to C(II) and S(VI) and ultimately to CO
3
2−
, SO
4
2−
, F
−
, and H
2
, since C(II) (as formate) reduces aqueous alkali to H
2
under the reaction conditions. No decomposition of NaTFMS could be detected after 24 h at 620 K in neutral aqueous solution. HTFMS reduces certain aqueous species at significant rates at moderate temperatures (e.g., Fe(III) to Fe(II) at 470 K), and metals which depend on oxide films for their corrosion resistance are attacked by HTFMS even at 294 K (e.g., Ti dissolves giving Ti(H
2
O)
6
3+
). Otherwise, HTFMS and its salts have good potentialities as inert electrolytes for aqueous studies at high temperatures.</description><identifier>ISSN: 0008-4042</identifier><identifier>EISSN: 1480-3291</identifier><identifier>DOI: 10.1139/v75-433</identifier><language>eng</language><publisher>Ottawa, Canada: NRC Research Press</publisher><ispartof>Canadian journal of chemistry, 1975-10, Vol.53 (20), p.3053-3059</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c320t-ae12514c3252260deeb197244e7f15f6642145cac5c386f7e4391e107ebcef563</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://cdnsciencepub.com/doi/pdf/10.1139/v75-433$$EPDF$$P50$$Gnrcresearch$$H</linktopdf><linktohtml>$$Uhttps://cdnsciencepub.com/doi/full/10.1139/v75-433$$EHTML$$P50$$Gnrcresearch$$H</linktohtml><link.rule.ids>314,780,784,2930,27923,27924,64427,65005</link.rule.ids></links><search><creatorcontrib>Fabes, Leonard</creatorcontrib><creatorcontrib>Swaddle, Thomas Wilson</creatorcontrib><title>Reagents for High Temperature Aqueous Chemistry: Trifluoromethanesulfonic Acid and its Salts</title><title>Canadian journal of chemistry</title><addtitle>Revue canadienne de chimie</addtitle><description>The rate of decomposition of trifluoromethanesulfonic acid (HTFMS) in water is first order with respect to each of H
+
and TFMS
−
. The bimolecular rate coefficient k
H
can be represented by
at ionic strength 1.0 mol kg
−1
over the temperature range 571 < T < 593 K, although the decomposition occurs by two pathways of comparable importance, one leading to C(II) and S(VI) and the other to C(IV) and S(IV). In alkaline solution, the rate of decomposition of TFMS
−
is first order in each of TFMS
−
and OH
−
, and the bimolecular rate coefficients k
OH
at ionic strength 2.3 are given by
This represents a single reaction pathway leading initially to C(II) and S(VI) and ultimately to CO
3
2−
, SO
4
2−
, F
−
, and H
2
, since C(II) (as formate) reduces aqueous alkali to H
2
under the reaction conditions. No decomposition of NaTFMS could be detected after 24 h at 620 K in neutral aqueous solution. HTFMS reduces certain aqueous species at significant rates at moderate temperatures (e.g., Fe(III) to Fe(II) at 470 K), and metals which depend on oxide films for their corrosion resistance are attacked by HTFMS even at 294 K (e.g., Ti dissolves giving Ti(H
2
O)
6
3+
). Otherwise, HTFMS and its salts have good potentialities as inert electrolytes for aqueous studies at high temperatures.</description><issn>0008-4042</issn><issn>1480-3291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1975</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLw0AURgdRsFbxL8xKQYjOMw93pagVCoLGnRCmkzvNSF7eSYT-eyPtVlcfHxzO4hByydkt5zK7-050pKQ8IjOuUhZJkfFjMmOMpZFiSpySsxA-p5swoWfk4xXMFtohUNchXfltRXNoekAzjAh08TVCNwa6rKDxYcDdPc3Ru3rssGtgqEwLYaxd13pLF9aX1LQl9ZPtzdRDOCcnztQBLg47J--PD_lyFa1fnp6Xi3VkpWBDZIALzdV0tBAxKwE2PEuEUpA4rl0cK8GVtsZqK9PYJaBkxoGzBDYWnI7lnFzvvRa7EBBc0aNvDO4KzorfKMUUpZiiTOTNnmzRIgQwaKt_4Ku_4QNU9KWTP6iBcL0</recordid><startdate>19751015</startdate><enddate>19751015</enddate><creator>Fabes, Leonard</creator><creator>Swaddle, Thomas Wilson</creator><general>NRC Research Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19751015</creationdate><title>Reagents for High Temperature Aqueous Chemistry: Trifluoromethanesulfonic Acid and its Salts</title><author>Fabes, Leonard ; Swaddle, Thomas Wilson</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-ae12514c3252260deeb197244e7f15f6642145cac5c386f7e4391e107ebcef563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fabes, Leonard</creatorcontrib><creatorcontrib>Swaddle, Thomas Wilson</creatorcontrib><collection>CrossRef</collection><jtitle>Canadian journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fabes, Leonard</au><au>Swaddle, Thomas Wilson</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reagents for High Temperature Aqueous Chemistry: Trifluoromethanesulfonic Acid and its Salts</atitle><jtitle>Canadian journal of chemistry</jtitle><addtitle>Revue canadienne de chimie</addtitle><date>1975-10-15</date><risdate>1975</risdate><volume>53</volume><issue>20</issue><spage>3053</spage><epage>3059</epage><pages>3053-3059</pages><issn>0008-4042</issn><eissn>1480-3291</eissn><abstract>The rate of decomposition of trifluoromethanesulfonic acid (HTFMS) in water is first order with respect to each of H
+
and TFMS
−
. The bimolecular rate coefficient k
H
can be represented by
at ionic strength 1.0 mol kg
−1
over the temperature range 571 < T < 593 K, although the decomposition occurs by two pathways of comparable importance, one leading to C(II) and S(VI) and the other to C(IV) and S(IV). In alkaline solution, the rate of decomposition of TFMS
−
is first order in each of TFMS
−
and OH
−
, and the bimolecular rate coefficients k
OH
at ionic strength 2.3 are given by
This represents a single reaction pathway leading initially to C(II) and S(VI) and ultimately to CO
3
2−
, SO
4
2−
, F
−
, and H
2
, since C(II) (as formate) reduces aqueous alkali to H
2
under the reaction conditions. No decomposition of NaTFMS could be detected after 24 h at 620 K in neutral aqueous solution. HTFMS reduces certain aqueous species at significant rates at moderate temperatures (e.g., Fe(III) to Fe(II) at 470 K), and metals which depend on oxide films for their corrosion resistance are attacked by HTFMS even at 294 K (e.g., Ti dissolves giving Ti(H
2
O)
6
3+
). Otherwise, HTFMS and its salts have good potentialities as inert electrolytes for aqueous studies at high temperatures.</abstract><cop>Ottawa, Canada</cop><pub>NRC Research Press</pub><doi>10.1139/v75-433</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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issn | 0008-4042 1480-3291 |
language | eng |
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source | NRC Research Press; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry |
title | Reagents for High Temperature Aqueous Chemistry: Trifluoromethanesulfonic Acid and its Salts |
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