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    <subfield code="a">10.1002/kin.21760</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">ART-2025-140340</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Glarborg, Peter</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Decomposition of CH3NH2: Implications for CHx/NHy radical–radical reactions</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2025</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Experiments on methylamine () decomposition in shock tubes, flow reactors, and batch reactors have been re‐examined to improve the understanding of hydrocarbon/amine interactions and constrain rate constants for  +  reactions. In high‐temperature shock tube experiments, the rapid thermal dissociation of  provides a fairly clean source of  and  radicals, allowing an assessment of reactions of  with  and NH. At the lower temperatures in batch and flow reactors,  is mostly consumed by reaction with H to form  + ; these results are useful in determining the fate of the  radical. Interpretation of these data, along with flow reactor data for the /H system at lower temperature, indicates that at temperatures up to about 1400 K at atmospheric pressure and above 2000 K at 100 atm, the  +  reaction forms mainly methylamine. At sufficiently high temperature, H‐abstraction to form  + NH and addition–elimination to form  + H become competitive. The  + NH reaction, with a rate constant close to collision frequency, forms  + H, also leading into the hydrocarbon amine pool. Thus, methylamine can be expected to be an important intermediate in co‐combustion of natural gas and ammonia, and more work on the chemistry of  is desirable.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/955413/EU/Sustainable technologies for future long distance shipping towards complete decarbonisation/ENGIMMONIA</subfield>
    <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 955413-ENGIMMONIA</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MICINN/PID2021-12432OB-I00</subfield>
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    <subfield code="u">http://creativecommons.org/licenses/by/3.0/es/</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Alzueta, Maria U.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-4679-5761</subfield>
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    <subfield code="1">5005</subfield>
    <subfield code="2">790</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Ing.Quím.Tecnol.Med.Amb.</subfield>
    <subfield code="c">Área Tecnologi. Medio Ambiente</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">57, 1 (2025), 77-90</subfield>
    <subfield code="p">Int. j. chem. kinet.</subfield>
    <subfield code="t">INTERNATIONAL JOURNAL OF CHEMICAL KINETICS</subfield>
    <subfield code="x">0538-8066</subfield>
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    <subfield code="a">2024-12-20-12:05:37</subfield>
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