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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Kinetics and Catalysis</journal-id><journal-title-group><journal-title xml:lang="en">Kinetics and Catalysis</journal-title><trans-title-group xml:lang="ru"><trans-title>Кинетика и катализ</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0453-8811</issn><issn publication-format="electronic">3034-5413</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">660314</article-id><article-id pub-id-type="doi">10.31857/S0453881123050039</article-id><article-id pub-id-type="edn">MYRFJB</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Bimetallic Heterogeneous Catalysts for the Oxidation of Sulfur-Containing Compounds with Hydrogen Peroxide</article-title><trans-title-group xml:lang="ru"><trans-title>Биметаллические гетерогенные катализаторы окисления серосодержащих соединений пероксидом водорода</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Gul</surname><given-names>O. O.</given-names></name><name xml:lang="ru"><surname>Гуль</surname><given-names>О. О.</given-names></name></name-alternatives><email>lesi00gul@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Polikarpova</surname><given-names>P. D.</given-names></name><name xml:lang="ru"><surname>Поликарпова</surname><given-names>П. Д.</given-names></name></name-alternatives><email>polikarpova@petrol.chem.msu.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Akopyan</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Акопян</surname><given-names>А. В.</given-names></name></name-alternatives><email>polikarpova@petrol.chem.msu.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Anisimov</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Анисимов</surname><given-names>А. В.</given-names></name></name-alternatives><email>polikarpova@petrol.chem.msu.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Lomonosov Moscow State University, Department of Petroleum Chemistry 
and Organic Catalysis, Faculty of Chemistry</institution></aff><aff><institution xml:lang="ru">Московский государственный университет им. М.В. Ломоносова, кафедра химии нефти и органического катализа, химический факультет, ГСП-1</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-09-01" publication-format="electronic"><day>01</day><month>09</month><year>2023</year></pub-date><volume>64</volume><issue>5</issue><fpage>609</fpage><lpage>617</lpage><history><date date-type="received" iso-8601-date="2025-02-22"><day>22</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, О.О. Гуль, П.Д. Поликарпова, А.В. Акопян, А.В. Анисимов</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, О.О. Гуль, П.Д. Поликарпова, А.В. Акопян, А.В. Анисимов</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">О.О. Гуль, П.Д. Поликарпова, А.В. Акопян, А.В. Анисимов</copyright-holder><copyright-holder xml:lang="ru">О.О. Гуль, П.Д. Поликарпова, А.В. Акопян, А.В. Анисимов</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/0453-8811/article/view/660314">https://journals.eco-vector.com/0453-8811/article/view/660314</self-uri><abstract xml:lang="en"><p id="idm45181324086464">Bimetallic heterogeneous catalysts based on SBA-15 containing molybdenum and iron oxides were studied in the oxidation reactions of model mixtures of organosulfur compounds. Iron additive (in the form of iron(III) oxide) in the amount of 0.05 wt % to the catalyst 5%Mo/SBA-15 turns out to be the most effective. The catalysts were confirmed by a complex of physicochemical methods: low-temperature adsorption-desorption of nitrogen, X-ray phase analysis, transmission electron microscopy, X-ray photoelectron spectroscopy. The influence of the main oxidation parameters (reaction time, temperature, composition and amount of catalyst, amount of oxidizer) on the conversion of dibenzothiophene as a component of the model mixture weas investigated. Optimal oxidation conditions that allow to achieve total transformation of the substrate were selected: H<sub>2</sub>O<sub>2</sub> : S = 2 : 1, 0.5 wt % of the catalyst FeMo/SBA-15, 60 min, 60°C; catalysts can be used for at least 5 cycles without loss of activity during their intermediate washing from oxidation products.</p></abstract><trans-abstract xml:lang="ru"><p id="idm45181324084512">Биметаллические гетерогенные катализаторы на основе SBA-15, содержащие в своем составе оксиды молибдена и железа, исследованы в реакциях окисления модельных смесей сероорганических соединений. Добавка железа (в виде оксида железа(III)) в количестве 0.05 мас. % к катализатору 5% Мо/SBA-15 была наиболее эффективной. исследованы комплексом физико-химических методов: низкотемпературная адсорбция–десорбция азота, рентгенофазовый анализ, просвечивающая электронная микроскопия, рентгеновская фотоэлектронная спектроскопия. Оценено влияние основных параметров окисления (время Катализаторы реакции, температура, состав и количество катализатора, количество окислителя) на конверсию дибензотиофена как компонента модельной смеси. Подобраны оптимальные условия окисления, позволяющие достичь исчерпывающего превращения субстрата: мольное отношение H<sub>2</sub>O<sub>2</sub> : S = 2 : 1, 0.5 мас. % катализатора FeMo/SBA-15, 60 мин, 60°C. Катализаторы могут быть использованы не менее 5 циклов без потери активности при промежуточной промывке от продуктов окисления.</p></trans-abstract><kwd-group xml:lang="en"><kwd>oxidative desulfurization</kwd><kwd>dibenzothiophene</kwd><kwd>hydrogen peroxide</kwd><kwd>transition metal oxides</kwd><kwd>bimetallic catalyst</kwd><kwd>SBA-15</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>окислительное обессеривание</kwd><kwd>дибензотиофен</kwd><kwd>пероксид водорода</kwd><kwd>оксиды переходных металлов</kwd><kwd>биметаллический катализатор</kwd><kwd>SBA-15</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Zhang M., Liu J., Li H., Wei Y., Fu Y., Liao W., Zhu L., Chen G., Zhu W., Li H. // Appl. Catal. B: Environ. 2020. V. 271. P. 118936.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Lim X., Ong W. // Nanoscale Horizons. 2021. V. 6. № 8. 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