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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">alternative</journal-id><journal-title-group><journal-title xml:lang="ru">Альтернативная энергетика и экология (ISJAEE)</journal-title><trans-title-group xml:lang="en"><trans-title>Alternative Energy and Ecology (ISJAEE)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1608-8298</issn><publisher><publisher-name>Международный издательский дом научной периодики "Спейс</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15518/isjaee.2019.16-18.27-36</article-id><article-id custom-type="elpub" pub-id-type="custom">alternative-1726</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>Водородная экономика</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Hydrogen Economy</subject></subj-group></article-categories><title-group><article-title>Низкотемпературное парциальное окисление этанола на катализаторе Ni/ZnO</article-title><trans-title-group xml:lang="en"><trans-title>Low-temperature partial oxidation of ethanol on Ni/ZnO catalyst</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6609-399X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лапин</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Lapin</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. техн. наук, ст. научный сотрудник,</p><p>д. 6, ул. Академика Осипьяна, г. Черноголовка, Московская обл., 142432</p></bio><bio xml:lang="en"><p>Ph.D. in Engineering, Senior Researcher,</p><p>6 Academician Osipyan Str., Chernogolovka, Moscow Reg., 142432</p></bio><email xlink:type="simple">lapin@iptm.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9717-8865</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гринько</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Grinko</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. хим. наук, мл. научный сотрудник,</p><p>д. 6, ул. Академика Осипьяна, г. Черноголовка, Московская обл., 142432</p></bio><bio xml:lang="en"><p>Ph.D. in Chemistry, Junior Researcher,</p><p>6 Academician Osipyan Str., Chernogolovka, Moscow Reg., 142432</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9289-6435</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бежок</surname><given-names>В. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Bezhok</surname><given-names>V. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>мл. научный сотрудник,</p><p>д. 6, ул. Академика Осипьяна, г. Черноголовка, Московская обл., 142432</p></bio><bio xml:lang="en"><p>Junior Researcher,</p><p>6 Academician Osipyan Str., Chernogolovka, Moscow Reg., 142432</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вяткин</surname><given-names>А. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Vyatkin</surname><given-names>A. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р физ.-мат. наук, профессор, зам. директора,</p><p>д. 6, ул. Академика Осипьяна, г. Черноголовка, Московская обл., 142432</p></bio><bio xml:lang="en"><p>D.Sc. in Physics and Mathematics, Professor, Deputy Director,</p><p>6 Academician Osipyan Str., Chernogolovka, Moscow Reg., 142432</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУН Институт проблем технологии микроэлектроники и особочистых материалов Российской академии наук (ИПТМ РАН)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Microelectronics Technology and High Purity Materials (IMT RAS)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>29</day><month>07</month><year>2019</year></pub-date><volume>0</volume><issue>16-18</issue><fpage>27</fpage><lpage>36</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Международный издательский дом научной периодики "Спейс, 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Международный издательский дом научной периодики "Спейс</copyright-holder><copyright-holder xml:lang="en">Международный издательский дом научной периодики "Спейс</copyright-holder><license xlink:href="https://www.isjaee.com/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.isjaee.com/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.isjaee.com/jour/article/view/1726">https://www.isjaee.com/jour/article/view/1726</self-uri><abstract><p>Исследован процесс парциального окисления этанола в кварцевом микрореакторе при атмосферном давлении в области температур 300–450 °С на никелевом катализаторе (20 мас %), нанесенном на оксид цинка. Ректификат этанола (азеотропная смесь состава 95,6 мас.% этанола и 4,4 мас.% воды) подавался в реактор со скоростью 0,4–1,3 г/час перистальтическим насосом сначала в испаритель, а затем в виде газовой фазы – в реактор. В качестве источника кислорода использовали воздух, который подавался воздушным насосом в реактор, и его поток регулировался ротаметром, чтобы молярное соотношение «кислород – этанол» изменялось в интервале 0,45–2,0. Никелевый катализатор приготовлялся пропиткой промышленного порошка оксида цинка нитратом никеля с последующим прокаливанием и восстановлением оксида никеля до металлического никеля. Анализ газообразных продуктов осуществляли на газовом хроматографе «Цвет-500», детектор – катарометр.</p><p>Показано, что разработанный ранее катализатор Ni/ZnO имеет высокую эффективность при парциальном окислении этанола в области низких температур. Основными продуктами этого процесса являются водород, метан, монооксид и диоксид углерода. С увеличением молярного соотношения «кислород – этанол», содержание водорода в продуктах процесса уменьшается (от 60 об.% до 25 об.%), а двуокиси углерода, наоборот, увеличивается (от 26 об.% до 65 об.%). Выход водорода составлял при температуре 450 °С 1 моль на 1 моль этанола.</p><p>Монооксид углерода наблюдается при малом соотношении «кислород – этанол» (до 0,85). Установлено, что при большем соотношении монооксид углерода отсутствует во всей исследованной области температур. Конверсия этанола протекает интенсивно, и уже при температуре 450 °С этанол конверсирован практически полностью. Большое содержание метана (20–30 об.%) в продуктах реформинга указывает на то, что начальной стадией процесса является окисление этанола с последующим разложением образующегося ацетальдегида на метан и монооксид углерода. Незначительное содержание воды в питающей смеси приводит к практически полному отсутствию шифт-реакции, при этом моноокись углерода окисляется кислородом до двуокиси углерода. Пониженное содержание метана в сравнении с процессом водно-парового реформинга этанола может быть объяснено частичным его окислением до двуокиси углерода, о чем свидетельствует высокое содержание последнего в продуктах реформинга. </p></abstract><trans-abstract xml:lang="en"><p>The paper investigates the partial oxidation of ethanol process in a quartz microreactor at atmospheric pressure in the temperature range 300–450 °C on a nickel catalyst (20 wt%) deposited on zinc oxide. Rectified ethanol (an azeotropic mixture of 95.6 wt.% ethanol and 4.4 wt.% water) is fed into the reactor at a rate of 0.4–1.3 g / hour by a peristaltic pump, first into the evaporator, and then as a gas phase into the reactor. Air is used as a source of oxygen which is supplied by an air pump to the reactor and its flow is controlled by a rotameter so that the oxygen-ethanol molar ratio varied between 0.45 and 2.0. The nickel catalyst is prepared by impregnating industrial zinc oxide powder with nickel nitrate, followed by calcination and reduction of nickel oxide to metallic nickel. Analysis of gaseous products is performed on a Tsvet-500 gas chromatograph. The detector is a katharometer.</p><p>A catalyst Ni/ZnO developed earlier is shown to have high efficiency in the partial oxidation of ethanol at low temperatures. The main products of this process are hydrogen, methane, carbon monoxide and dioxide. With an increase in the oxygen-ethanol molar ratio, the hydrogen content in the products of the process decreases (from 60 to 25 vol.%), carbon dioxide, on the contrary, increases (26 to 65 vol.%). The hydrogen yield is 1 mol per 1 mol of ethanol at a temperature of 450 °C.</p><p>Carbon monoxide is observed with a low ratio of oxygen-ethanol (up to 0.85). With a higher ratio, carbon monoxide is absent in the entire temperature range studied. The conversion of ethanol proceeds intensively and already at a temperature of 450 °C ethanol is converted almost completely. A high methane content (20–30% vol.%) in reforming products indicates that the initial stage of the process is the oxidation of ethanol followed by decomposition of the resulting acetaldehyde into methane and carbon monoxide.</p><p>The insignificant water content in the supply mixture leads to an almost complete absence of a shift reaction. Carbon monoxide is then oxidized with oxygen to carbon dioxide. The reduced methane content in comparison with the process of water-steam ethanol reforming can be explained by its partial oxidation to carbon dioxide, which explains the high content of the latter in reforming products. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>низкотемпературное парциальное окисление</kwd><kwd>этанол</kwd><kwd>никелевый катализатор</kwd><kwd>водород</kwd><kwd>метан</kwd><kwd>кислород</kwd><kwd>диоксид углерода</kwd><kwd>монооксид углерода</kwd><kwd>микрореактор</kwd><kwd>конверсия</kwd><kwd>реформинг</kwd></kwd-group><kwd-group xml:lang="en"><kwd>low-temperature partial oxidation</kwd><kwd>ethanol</kwd><kwd>nickel catalyst</kwd><kwd>hydrogen</kwd><kwd>methane</kwd><kwd>oxygen</kwd><kwd>carbon dioxide</kwd><kwd>carbon monoxide</kwd><kwd>microreactor</kwd><kwd>conversion</kwd><kwd>reforming</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена по государственному заданию № 007-00220-18-00.</funding-statement><funding-statement xml:lang="en">The work was performed according to the state task number 007-00220-18-00.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Edwards, P.P. 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