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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">83155</article-id>
   <article-id pub-id-type="doi">10.52957/27821900_2020_01_161</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">Study of cyclohexylbenzene liquid-phase oxidation products composition</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Study of cyclohexylbenzene liquid-phase oxidation products composition</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <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>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>Коршунова</surname>
       <given-names>Александра Игоревна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Korshunova</surname>
       <given-names>Aleksandra Igorevna</given-names>
      </name>
     </name-alternatives>
     <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="2020-12-31T00:00:00+03:00">
    <day>31</day>
    <month>12</month>
    <year>2020</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2020-12-31T00:00:00+03:00">
    <day>31</day>
    <month>12</month>
    <year>2020</year>
   </pub-date>
   <volume>1</volume>
   <issue>1</issue>
   <fpage>161</fpage>
   <lpage>167</lpage>
   <history>
    <date date-type="received" iso-8601-date="2020-09-14T00:00:00+03:00">
     <day>14</day>
     <month>09</month>
     <year>2020</year>
    </date>
    <date date-type="accepted" iso-8601-date="2020-10-19T00:00:00+03:00">
     <day>19</day>
     <month>10</month>
     <year>2020</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/83155/view">https://chemintech.ru/en/nauka/article/83155/view</self-uri>
   <abstract xml:lang="ru">
    <p>The paper examines the contents of products of liquid-phase oxidation of cyclohexylbenzene. The study proves the existence of tertiary and secondary hydroperoxide in the oxidation products of cyclohexylbenzene. The hydroperoxides were determined directly by NMR1H-spectroscopy and indirectly by their products of reduction to ketones and alcohols. By comparing integral intensities of tertiary and secondary cyclohexylbenzene hydroperoxide proton signals, we can assume that the content of the latter is approximately 15-20% of the total hydroperoxide content present in the cyclohexylbenzene oxidation products. The general scheme of oxidative transformations of cyclohexylbenzene is compiled based on the experimental data obtained and the existing knowledge of the essence of liquid-phase oxidation of alkylsubstituted aromatic and cycloaliphatic hydrocarbons. The study shows a considerable decrease in selectivity of oxidation process when cyclohexylbenzene conversion increases up to 40-50%.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The paper examines the contents of products of liquid-phase oxidation of cyclohexylbenzene. The study proves the existence of tertiary and secondary hydroperoxide in the oxidation products of cyclohexylbenzene. The hydroperoxides were determined directly by NMR1H-spectroscopy and indirectly by their products of reduction to ketones and alcohols. By comparing integral intensities of tertiary and secondary cyclohexylbenzene hydroperoxide proton signals, we can assume that the content of the latter is approximately 15-20% of the total hydroperoxide content present in the cyclohexylbenzene oxidation products. The general scheme of oxidative transformations of cyclohexylbenzene is compiled based on the experimental data obtained and the existing knowledge of the essence of liquid-phase oxidation of alkylsubstituted aromatic and cycloaliphatic hydrocarbons. The study shows a considerable decrease in selectivity of oxidation process when cyclohexylbenzene conversion increases up to 40-50%.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>cyclohexylbenzene</kwd>
    <kwd>liquid-phase oxidation</kwd>
    <kwd>tertiary cyclohexylbenzene hydroperoxide</kwd>
    <kwd>secondary cyclohexylbenzene hydroperoxide</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
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