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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Herald of Technological University</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Herald of Technological University</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>ВЕСТНИК ТЕХНОЛОГИЧЕСКОГО УНИВЕРСИТЕТА</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">3034-4689</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">62801</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>ХИМИЯ, ТЕХНОЛОГИЯ И ИСПОЛЬЗОВАНИЕ ПОЛИМЕРОВ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject></subject>
    </subj-group>
    <subj-group>
     <subject>ХИМИЯ, ТЕХНОЛОГИЯ И ИСПОЛЬЗОВАНИЕ ПОЛИМЕРОВ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">ПОЛУЧЕНИЕ 4,4'-БИС(2,6-ДИ-ТРЕТ-БУТИЛФЕНОЛА) И ПОЛИХИНОНА В РЕАКЦИИ ЩЕЛОЧНОГО ОКИСЛИТЕЛЬНОГО ДЕГИДРИРОВАНИЯ ГИДРОХИНОНА 3,3',5,5'-ТЕТРА-ТРЕТ-БУТИЛДИФЕНОХИНОНОМ</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>ПОЛУЧЕНИЕ 4,4'-БИС(2,6-ДИ-ТРЕТ-БУТИЛФЕНОЛА) И ПОЛИХИНОНА В РЕАКЦИИ ЩЕЛОЧНОГО ОКИСЛИТЕЛЬНОГО ДЕГИДРИРОВАНИЯ ГИДРОХИНОНА 3,3',5,5'-ТЕТРА-ТРЕТ-БУТИЛДИФЕНОХИНОНОМ</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Ахмадуллин</surname>
       <given-names>Р М</given-names>
      </name>
      <name xml:lang="en">
       <surname>Ахмадуллин</surname>
       <given-names>Р М</given-names>
      </name>
     </name-alternatives>
     <email>ahmadullinr@gmail.com</email>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Гатиятуллин</surname>
       <given-names>Д Р</given-names>
      </name>
      <name xml:lang="en">
       <surname>Гатиятуллин</surname>
       <given-names>Д Р</given-names>
      </name>
     </name-alternatives>
     <email>gatiyatullin@mail.ru</email>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Ахмадуллина</surname>
       <given-names>А Г</given-names>
      </name>
      <name xml:lang="en">
       <surname>Ахмадуллина</surname>
       <given-names>А Г</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Верижников</surname>
       <given-names>Л В</given-names>
      </name>
      <name xml:lang="en">
       <surname>Верижников</surname>
       <given-names>Л В</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-4"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Мукменева</surname>
       <given-names>Н А</given-names>
      </name>
      <name xml:lang="en">
       <surname>Мукменева</surname>
       <given-names>Н А</given-names>
      </name>
     </name-alternatives>
     <email>nmukmeneva@mail.ru</email>
     <xref ref-type="aff" rid="aff-5"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">КНИТУ</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">КНИТУ</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">КНИТУ</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">КНИТУ</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-3">
    <aff>
     <institution xml:lang="ru">предприниматель</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">предприниматель</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-4">
    <aff>
     <institution xml:lang="ru">предприниматель</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">предприниматель</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-5">
    <aff>
     <institution xml:lang="ru">КНИТУ</institution>
     <country>ru</country>
    </aff>
    <aff>
     <institution xml:lang="en">КНИТУ</institution>
     <country>ru</country>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2025-08-01T14:16:21+03:00">
    <day>01</day>
    <month>08</month>
    <year>2025</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2025-08-01T14:16:21+03:00">
    <day>01</day>
    <month>08</month>
    <year>2025</year>
   </pub-date>
   <volume>17</volume>
   <issue>6</issue>
   <fpage>160</fpage>
   <lpage>163</lpage>
   <history>
    <date date-type="received" iso-8601-date="2023-04-20T15:23:31+03:00">
     <day>20</day>
     <month>04</month>
     <year>2023</year>
    </date>
   </history>
   <self-uri xlink:href="https://vestniktu.ru/en/nauka/article/62801/view">https://vestniktu.ru/en/nauka/article/62801/view</self-uri>
   <abstract xml:lang="ru">
    <p>В работе рассмотрен способ получения 4,4'-бис(2,6-ди-трет-бутилфенола) путем дегидрирования гидрохинона 3,3',5,5'-тетра-трет-бутилдифенохиноном в толуоле в присутствии щелочного катализатора. В результате достигнут высокий выход 4,4'-бис(2,6-ди-трет-бутилфенола) и получен второй продукт полимерной природы «полихинон». </p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The paper considers process for 4,4'-bis(2,6-di-tert-butylphenol) preparing by dehydrogenation of hydroquinone with 3,3',5,5'-tetra-tert-butyldiphenoquinone in toluene in the presence of alkaline catalyst. As a result, high yield of 4,4'-bis(2,6-di-tert-butylphenol) is achieved and second product of polymeric nature - polyquinone is obtained. </p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>3</kwd>
    <kwd>3'</kwd>
    <kwd>5</kwd>
    <kwd>5'-тетра-трет-бутилдифенохинон</kwd>
    <kwd>4</kwd>
    <kwd>4'-бис(2</kwd>
    <kwd>6-ди-трет-бутилфенол)</kwd>
    <kwd>гидрохинон</kwd>
    <kwd>восстановление</kwd>
    <kwd>дегидрирование</kwd>
    <kwd>полихинон</kwd>
    <kwd>щелочной катализ</kwd>
    <kwd>3</kwd>
    <kwd>3'</kwd>
    <kwd>5</kwd>
    <kwd>5'-tetra-tert-butyldiphenoquinone</kwd>
    <kwd>4</kwd>
    <kwd>4'-bis(2</kwd>
    <kwd>6-di-tert-butylphenol)</kwd>
    <kwd>hydroquinone</kwd>
    <kwd>reduction</kwd>
    <kwd>dehydrogenation</kwd>
    <kwd>alkaline catalysis</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>3</kwd>
    <kwd>3'</kwd>
    <kwd>5</kwd>
    <kwd>5'-тетра-трет-бутилдифенохинон</kwd>
    <kwd>4</kwd>
    <kwd>4'-бис(2</kwd>
    <kwd>6-ди-трет-бутилфенол)</kwd>
    <kwd>гидрохинон</kwd>
    <kwd>восстановление</kwd>
    <kwd>дегидрирование</kwd>
    <kwd>полихинон</kwd>
    <kwd>щелочной катализ</kwd>
    <kwd>3</kwd>
    <kwd>3'</kwd>
    <kwd>5</kwd>
    <kwd>5'-tetra-tert-butyldiphenoquinone</kwd>
    <kwd>4</kwd>
    <kwd>4'-bis(2</kwd>
    <kwd>6-di-tert-butylphenol)</kwd>
    <kwd>hydroquinone</kwd>
    <kwd>reduction</kwd>
    <kwd>dehydrogenation</kwd>
    <kwd>alkaline catalysis</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
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