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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">From Chemistry Towards Technology Step-By-Step</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">From Chemistry Towards Technology Step-By-Step</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>От химии к технологии шаг за шагом</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="online">2782-1900</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">81468</article-id>
   <article-id pub-id-type="doi">10.52957/2782-1900-2024-4-4-89-99</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>Научные статьи</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>Scientific articles</subject>
    </subj-group>
    <subj-group>
     <subject>Научные статьи</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">Case study on 4-Isopropyl-ortho-xylene production</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Case study on 4-Isopropyl-ortho-xylene production</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Мазурин</surname>
       <given-names>Олег Анатольевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Mazurin</surname>
       <given-names>Oleg Anatolievich</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Шакун</surname>
       <given-names>Владимир Андреевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Shakun</surname>
       <given-names>Vladimir Andreevich</given-names>
      </name>
     </name-alternatives>
     <email>shakyh@mail.ru</email>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Нестерова</surname>
       <given-names>Татьяна Николаевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Nesterova</surname>
       <given-names>Tatiana Nikolaevna</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Востриков</surname>
       <given-names>Сергей Владимирович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Vostrikov</surname>
       <given-names>Sergey Vladimirovich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Курганова</surname>
       <given-names>Екатерина Анатольевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kurganova</surname>
       <given-names>Ekaterina Anatol'evna</given-names>
      </name>
     </name-alternatives>
     <email>kurganovaea@ystu.ru</email>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Кошель</surname>
       <given-names>Георгий Николаевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Koshel</surname>
       <given-names>Georgy Nikolaevich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>доктор химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
    <contrib contrib-type="author">
     <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0491-7452</contrib-id>
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Фролов</surname>
       <given-names>Александр Сергеевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Frolov</surname>
       <given-names>Aleksandr Sergeevich</given-names>
      </name>
     </name-alternatives>
     <email>frolovas@ystu.ru</email>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Honeywell Process Solutions</institution>
     <city>Москва</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Honeywell Process Solutions</institution>
     <city>Moscow</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">Самарский государственный технический университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Samara State Technical University</institution>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-3">
    <aff>
     <institution xml:lang="ru">Ярославский государственный технический университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Yaroslavl State Technical University</institution>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2023-12-23T00:00:00+03:00">
    <day>23</day>
    <month>12</month>
    <year>2023</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2023-12-23T00:00:00+03:00">
    <day>23</day>
    <month>12</month>
    <year>2023</year>
   </pub-date>
   <volume>4</volume>
   <issue>4</issue>
   <fpage>89</fpage>
   <lpage>99</lpage>
   <history>
    <date date-type="received" iso-8601-date="2023-11-03T00:00:00+03:00">
     <day>03</day>
     <month>11</month>
     <year>2023</year>
    </date>
    <date date-type="accepted" iso-8601-date="2023-11-29T00:00:00+03:00">
     <day>29</day>
     <month>11</month>
     <year>2023</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/81468/view">https://chemintech.ru/en/nauka/article/81468/view</self-uri>
   <abstract xml:lang="ru">
    <p>We have experimentally studied the alkylation reaction of o-xylene with propylene under kinetic control conditions followed by realkylation under thermodynamic control conditions. The paper provides an analysis of the alkylation reaction products obtained under kinetic control as well as kinetic analysis and thermodynamic analysis of the overalkylation process. The authors have considered the methyl group migration reactions during overalkylation and have given kinetic analyses of these reactions. We found that the optimal method for the preparation of 4 isopropyl-o-xylene is to conduct the process in two stages. The first one is a liquid-phase alkylation of o-xylene under kinetic control at 353 K. The second stage is liquid-phase realkylation of the obtained alkylation reaction mass until reaching thermodynamic equilibrium at a temperature range of 303-353 K under certain conditions. These conditions should ensure minimal migration of methyl groups, i.e. with minimum contact time and alkyl-/aryl- &lt; 0.5 ratio in the reaction products.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>We have experimentally studied the alkylation reaction of o-xylene with propylene under kinetic control conditions followed by realkylation under thermodynamic control conditions. The paper provides an analysis of the alkylation reaction products obtained under kinetic control as well as kinetic analysis and thermodynamic analysis of the overalkylation process. The authors have considered the methyl group migration reactions during overalkylation and have given kinetic analyses of these reactions. We found that the optimal method for the preparation of 4 isopropyl-o-xylene is to conduct the process in two stages. The first one is a liquid-phase alkylation of o-xylene under kinetic control at 353 K. The second stage is liquid-phase realkylation of the obtained alkylation reaction mass until reaching thermodynamic equilibrium at a temperature range of 303-353 K under certain conditions. These conditions should ensure minimal migration of methyl groups, i.e. with minimum contact time and alkyl-/aryl- &lt; 0.5 ratio in the reaction products.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>alkylation</kwd>
    <kwd>realkylation</kwd>
    <kwd>propylene</kwd>
    <kwd>sulphocationics</kwd>
    <kwd>o-xylene</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
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 <back>
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