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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="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">catal</journal-id><journal-title-group><journal-title xml:lang="ru">Катализ в промышленности</journal-title><trans-title-group xml:lang="en"><trans-title>Kataliz v promyshlennosti</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1816-0387</issn><issn pub-type="epub">2413-6476</issn><publisher><publisher-name>LLC "KALVIS"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18412/1816-0387-2017-3-236-242</article-id><article-id custom-type="elpub" pub-id-type="custom">catal-461</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="ru"><subject>ОТЕЧЕСТВЕННЫЕ КАТАЛИЗАТОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>DOMESTIC CATALYST</subject></subj-group></article-categories><title-group><article-title>Новый катализатор гидроизомеризации н-алканов, модифицированный наноразмерными карбидами молибдена, и его каталитические свойства в процеcсе гидроизомеризации дизельных фракций. Часть 2. Приготовление бифункциональных катализаторов гидроизомеризации</article-title><trans-title-group xml:lang="en"><trans-title>New Catalyst Modified with Nanosize Molybdenum Carbides for Hydroisomerization of n-Alkane, its Catalytic Behavior in the Process of Hydroisomerization of Diesel Fractions. Part 2. Preparation of Hydroisomerization Bifunctional Catalysts</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>Ечевский</surname><given-names>Г. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Echevsky</surname><given-names>G. V.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.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>Токтарев</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Toktarev</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.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>Аксенов</surname><given-names>Д. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Aksenov</surname><given-names>D. G.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.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>Коденев</surname><given-names>Е. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Kodenev</surname><given-names>E. G.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт катализа им. Г.К. Борескова СО РАН, Новосибирск</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Boreskov Institute of Catalysis, Novosibirsk</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>22</day><month>09</month><year>2017</year></pub-date><volume>17</volume><issue>3</issue><fpage>236</fpage><lpage>242</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; LLC "KALVIS", 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">LLC "KALVIS"</copyright-holder><copyright-holder xml:lang="en">LLC "KALVIS"</copyright-holder><license xlink:href="https://www.catalysis-kalvis.ru/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.catalysis-kalvis.ru/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.catalysis-kalvis.ru/jour/article/view/461">https://www.catalysis-kalvis.ru/jour/article/view/461</self-uri><abstract><p> </p><p>Цель данной работы – разработка нового катализатора гидроизомеризации на основе карбидов молибдена, устойчивого к воздействию сернистых соединений и обеспечивающего получение низкозастывающих дизельных топлив с такими же показателями, как при использовании платиносодержащих катализаторов. В первой части работы были синтезированы и изучены носители различной пористой структуры и кислотности (Beta, ZSM-5, ZSM-12, SAPO-31). Во второй части работы исследованы бифункциональные катализаторы, приготовленные модифицированием этих носителей наноразмерными карбидами молибдена. Содержание Мо2С в образцах одинаково (10 % в пересчете на МоО3). Проведено испытание катализаторов в модельной реакции гидроизомеризации н-декана. Наиболее эффективным оказался катализатор на основе силикоалюмофосфата ATO (SAPO-31). С целью оптимизации его состава приготовлены укрупненные партии образцов с разным содержанием Мо2С (5, 7 и 10 % в пересчете на МоО3). Исследованы их каталитические свойства в процессе гидроизомеризации реальных дизельных фракций. Выявлено оптимальное содержание Мо2С (7 мас.%) в бифункциональном катализаторе.</p></abstract><trans-abstract xml:lang="en"><p>The studies were aimed at the development of hydroisomerization catalysts based on nanosize molybdenum carbides. These catalysts were expected to be resistant to sulfur compounds and applicable for synthesis of low pour point diesel fuels similar in parameters to the fuel synthesized over platinum catalysts. Part I dealt with synthesis and characterization of supports with different porous structures and acidities (Beta, ZSM-5, ZSM-12, SAPO-31). Part 2 of the work was devoted to studies of bifunctional catalysts prepared by modifying these supports with nanosize molybdenum carbides. All the samples bore identical amounts of Mo2C (10 % expressed in terms of the equivalent amount of MoO3). The catalysts were tested using a model reaction of isomerization of n-decane. The catalyst based on silicoaluminophosphate ATO (SAPO-31) was most active to isomerization. Larger batches of the catalysts with different Mo2C contents (5, 7 and 10 expressed in terms of the equivalent amount of MoO3) were prepared to optimize the composition. The catalytic properties were studied using hydroisomerization of actual diesel fractions. The optimal content of Mo2C (7 wt %) in the bifunctional catalyst was determined.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>молибден</kwd><kwd>карбиды</kwd><kwd>кислотный носитель</kwd><kwd>цеолиты</kwd><kwd>силикоалюмосиликаты</kwd><kwd>катализатор</kwd><kwd>гидроизомеризация</kwd><kwd>дизельные топлива</kwd></kwd-group><kwd-group xml:lang="en"><kwd>molybdenum</kwd><kwd>carbides</kwd><kwd>acidic support</kwd><kwd>zeolites</kwd><kwd>silicoaluminosilicates</kwd><kwd>catalyst</kwd><kwd>hydroisomerization</kwd><kwd>diesel fuel</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">Marafi M., Stanislaus A., Furimsky E. Handbook of Spent Hydroprocessing Catalyst // Elsevier Amsterdam, 2010.</mixed-citation><mixed-citation xml:lang="en">Marafi M., Stanislaus A., Furimsky E. Handbook of Spent Hydroprocessing Catalyst // Elsevier Amsterdam, 2010.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Уржунцев Г.А., Коденев Е.Г., Ечевский Г.В. // Катализ в промышленности. Т. 16. № 3. 2016. С. 31—37.</mixed-citation><mixed-citation xml:lang="en">Уржунцев Г.А., Коденев Е.Г., Ечевский Г.В. // Катализ в промышленности. Т. 16. № 3. 2016. С. 31—37.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
