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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">82437</article-id>
   <article-id pub-id-type="doi">10.52957/27821900_2022_01_88</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">The reaction of cyclohexylbenzene oxidation in the presence of solvents</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>The reaction of cyclohexylbenzene oxidation in the presence of solvents</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <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-1"/>
    </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-1"/>
    </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-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Кабанова</surname>
       <given-names>Виктория Сергеевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kabanova</surname>
       <given-names>Viktoriya Sergeevna</given-names>
      </name>
     </name-alternatives>
     <email>kabanovavs@ystu.ru</email>
     <bio xml:lang="ru">
      <p>аспирант химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>graduate student of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <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="2022-03-23T00:00:00+03:00">
    <day>23</day>
    <month>03</month>
    <year>2022</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2022-03-23T00:00:00+03:00">
    <day>23</day>
    <month>03</month>
    <year>2022</year>
   </pub-date>
   <volume>3</volume>
   <issue>1</issue>
   <fpage>88</fpage>
   <lpage>94</lpage>
   <history>
    <date date-type="received" iso-8601-date="2022-02-16T00:00:00+03:00">
     <day>16</day>
     <month>02</month>
     <year>2022</year>
    </date>
    <date date-type="accepted" iso-8601-date="2022-03-21T00:00:00+03:00">
     <day>21</day>
     <month>03</month>
     <year>2022</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/82437/view">https://chemintech.ru/en/nauka/article/82437/view</self-uri>
   <abstract xml:lang="ru">
    <p>The paper concerns the process of aerobic liquid-phase oxidation of cyclohexylbenzene to hydroperoxide in the presence of different solvents. It has been found that it is preferable to carry out the reaction in an acetonitrile medium. We investigate the effect of different process parameters on the oxidation of cyclohexylbenzene in this solvent. Based on the results of the research, conditions were chosen that make it possible to achieve a hydrocarbon conversion rate of 11% in 2.5 hours with a hydroperoxide formation selectivity of about 93%. The average oxidation rate of cyclohexylbenzene increases about 1.3 times in compare with the process carried out in the absence of solvent.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The paper concerns the process of aerobic liquid-phase oxidation of cyclohexylbenzene to hydroperoxide in the presence of different solvents. It has been found that it is preferable to carry out the reaction in an acetonitrile medium. We investigate the effect of different process parameters on the oxidation of cyclohexylbenzene in this solvent. Based on the results of the research, conditions were chosen that make it possible to achieve a hydrocarbon conversion rate of 11% in 2.5 hours with a hydroperoxide formation selectivity of about 93%. The average oxidation rate of cyclohexylbenzene increases about 1.3 times in compare with the process carried out in the absence of solvent.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>cyclohexylbenzene</kwd>
    <kwd>aerobic liquid phase oxidation</kwd>
    <kwd>cyclohexylbenzene hydroperoxide</kwd>
    <kwd>solvents for liquid phase oxidation processes</kwd>
    <kwd>acetonitrile</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
 <back>
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</article>
