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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">chemicallytech</journal-id><journal-title-group><journal-title xml:lang="en">Fine Chemical Technologies</journal-title><trans-title-group xml:lang="ru"><trans-title>Тонкие химические технологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2410-6593</issn><issn pub-type="epub">2686-7575</issn><publisher><publisher-name>MIREA – Russian Technological University (RTU MIREA).</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">chemicallytech-468</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHEMISTRY AND TECHNOLOGY OF INORGANIC MATERIALS</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ХИМИЯ И ТЕХНОЛОГИЯ НЕОРГАНИЧЕСКИХ МАТЕРИАЛОВ</subject></subj-group></article-categories><title-group><article-title>The patterns of liquid-phase hydrogen peroxide decomposition over transition metal oxides anchored on mesoporous carbon surface</article-title><trans-title-group xml:lang="ru"><trans-title>Закономерности жидкофазного разложения H2O2 в присутствии закрепленных на мезопористом углеродном носителе оксидов переходных металлов</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гордиенко</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gordienko</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кафедра Физической химии им. Я.К. Сыркина, аспирант</p></bio><email xlink:type="simple">gordienkoaa@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соколова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Sokolova</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кафедра Физической химии им. Я.К. Сыркина, аспирант</p></bio><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Флид</surname><given-names>В. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Flid</surname><given-names>V. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кафедра Физической химии им. Я.К. Сыркина, заведующий кафедрой</p></bio><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>МИТХТ им. М.В. Ломоносова, 119571, Москва, пр-т Вернадского, д. 86</institution><country>Россия</country></aff><aff xml:lang="en"><institution>M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>28</day><month>06</month><year>2014</year></pub-date><volume>9</volume><issue>3</issue><fpage>51</fpage><lpage>56</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Gordienko A.A., Sokolova A.A., Flid V.R., 2014</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="ru">Гордиенко А.А., Соколова А.А., Флид В.Р.</copyright-holder><copyright-holder xml:lang="en">Gordienko A.A., Sokolova A.A., Flid V.R.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.finechem-mirea.ru/jour/article/view/468">https://www.finechem-mirea.ru/jour/article/view/468</self-uri><abstract><p>The article is devoted to peculiarities of liquid phase hydrogen peroxide decomposition over transition metal (Ag, Cu, Rh, Pd, N or Co) oxides anchored on mesoporous carbon support. The values of activation energy (Ea) and frequency factor (k0) of the catalytic reaction have been determined with kinetic data at 25–70°C. The reaction rate has been established to depend on the strength of the bond between the transition metal anchored and reactive oxygen species adsorbed. The contribution of free radical mechanism has been estimated with inhibitors of free hydroxy (HO∙) and super-oxide (O2 - ) radicals, e.g., dimethylsulfoxide and potassium chloride, respectively. The mechanism of the liquid phase hydrogen peroxide decomposition over the anchored transition metal oxides has been suggested to involve the formation of surface oxygen-containing transition metal complexes, their decomposition being the limiting step of the reaction.</p></abstract><trans-abstract xml:lang="ru"><p>Выявлены кинетические закономерности разложения Н2О2 в присутствии закрепленных на мезопористом углеродном носителе Сибунит оксидов переходных металлов (Co, Rh, Ni, Pd, Cu и Ag). Катализаторы охарактеризованы методами низкотемпературной (-196ºС) физической адсорбции азота и хемосорбции СО при 35ºС. Скорость реакции каталитического разложения Н2О2 при 25-70ºС измерена волюмометрическим методом. Установлено, что кинетика разложения Н2О2 зависит от характера взаимодействия поверхностных активных центров с носителем и стабильности кислородсодержащих поверхностных комплексов. На основании экспериментальных данных по влиянию ДМСО и KCl на кинетику каталитического разложения Н2О2 оценен возможный вклад радикально-цепного механизма реакции.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>пероксид водорода</kwd><kwd>каталитическое разложение Н2О2</kwd><kwd>закрепленные на Сибуните оксиды переходных металлов</kwd></kwd-group><kwd-group xml:lang="en"><kwd>liquid phase hydrogen peroxide decomposition</kwd><kwd>anchored transition metal oxides</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Cota H.M., Katan T., Chin M., Schoenweis F.J. Decomposition of dilute hydroge peroxide in alkaline solution // Nature. 1964. V. 4951. P. 1281-1289.</mixed-citation><mixed-citation xml:lang="en">Cota H.M., Katan T., Chin M., Schoenweis F.J. Decomposition of dilute hydroge peroxide in alkaline solution // Nature. 1964. V. 4951. 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