<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T07:16:49Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/121916" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/121916</identifier><datestamp>2025-11-19T20:35:16Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478796</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Two Rate constant kinetic model for the chromium(III)-EDTA complexation reaction by numerical simulations</dc:title>
   <dc:creator>Pérez de Benito, Joaquín F.</dc:creator>
   <dc:subject>Crom</dc:subject>
   <dc:subject>Reaccions químiques</dc:subject>
   <dc:subject>Cinètica química</dc:subject>
   <dc:subject>Chromium</dc:subject>
   <dc:subject>Chemical reactions</dc:subject>
   <dc:subject>Chemical kinetics</dc:subject>
   <dc:description>The complexation reaction of Cr(III) ion in the presence of a large excess of EDTA does not follow a pseudo-first-order kinetics as sometimes suggested. There are two causes for the deviation from this simple behavior: the involvement of a long-lived intermediate, precluding the application of the steady-state approximation, and the autoinhibition provoked by the release of hydrogen ions from the organic ligand to the medium as the final Cr(III)-EDTA violet complex is formed. Numerical simulations have allowed obtaining for each kinetic experiment the values of two rate constants, k1 (corresponding to the formation of the long-lived intermediate from the reactants) and k2 (corresponding to the formation of the final complex product from the long-lived intermediate), as well as the number of hydrogens liberated per molecule of final complex product formed (Hkin). The results indicate that k1 is associated to a fast step (Ea = 87 ± 4 kJ mol-1) and k2 to a slow step (Ea = 120 ± 2 kJ mol-1), whereas the number of hydrogen ions lies within the range 0 &lt; Hkin &lt; 2 in all the kinetic runs. A mechanism in accordance with the experimental data has been proposed.</dc:description>
   <dc:date>2018-04-27T07:49:16Z</dc:date>
   <dc:date>2018-04-27T07:49:16Z</dc:date>
   <dc:date>2017-01-21</dc:date>
   <dc:date>2018-04-27T07:49:16Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:identifier>0538-8066</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/121916</dc:identifier>
   <dc:identifier>669296</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1002/kin.21070</dc:relation>
   <dc:relation>International Journal of Chemical Kinetics, 2017, vol. 49, p. 234-249</dc:relation>
   <dc:relation>https://doi.org/10.1002/kin.21070</dc:relation>
   <dc:rights>(c) Wiley, 2017</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>48 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Wiley</dc:publisher>
   <dc:source>Articles publicats en revistes (Ciència dels Materials i Química Física)</dc:source>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>