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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">10.18412/1816-0387-2020-6-433-455</article-id><article-id custom-type="elpub" pub-id-type="custom">catal-726</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>КАТАЛИЗ В ХИМИЧЕСКОЙ И НЕФТЕХИМИЧЕСКОЙ ПРОМЫШЛЕННОСТИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CATALYSIS IN CHEMICAL AND PETROCHEMICAL INDUSTRY</subject></subj-group></article-categories><title-group><article-title>Современные тенденции в области процессов переработки линейных альфа-олефинов в технологически значимые продукты. Часть 1</article-title><trans-title-group xml:lang="en"><trans-title>Modern trends in the processing of linear alpha olefins to technologically important products. Part 1</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>Голубь</surname><given-names>Ф. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Golub</surname><given-names>F. S.</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>Болотов</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Bolotov</surname><given-names>V. A.</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>Пармон</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Parmon</surname><given-names>V. N.</given-names></name></name-alternatives><email xlink:type="simple">ctls@kalvis.ru</email><xref ref-type="aff" rid="aff-2"/></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 SB RAS, Novosibirsk</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Институт катализа им. Г.К. Борескова СО РАН, Новосибирск; Новосибирский государственный университет (НГУ)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Boreskov Institute of Catalysis SB RAS, Novosibirsk</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>25</day><month>11</month><year>2020</year></pub-date><volume>20</volume><issue>6</issue><fpage>433</fpage><lpage>455</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; LLC "KALVIS", 2020</copyright-statement><copyright-year>2020</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/726">https://www.catalysis-kalvis.ru/jour/article/view/726</self-uri><abstract><p>Линейные альфа-олефины (ЛАО) представляют собой класс химических соединений, применяемых в производстве высоко востребованных продуктов, таких как пластификаторы, различные синтетические смазочные материалы, поверхностно-активные вещества и сополимеры с улучшенными эксплуатационными характеристиками. Мировое потребление производных ЛАО ежегодно увеличивается, что обуславливает высокую вовлеченность в сферу переработки ЛАО как специалистов научных учреждений и университетов, так и научно-исследовательских отделов промышленных компаний. Анализ научной литературы за последние 10 лет обнаружил отсутствие обзоров общего характера, обсуждающих вопросы переработки ЛАО. Обзор направлен на освещение последних тенденций в процессах, связанных с переработкой ЛАО, содержащих 4 и более атомов углерода, в технологически значимые производные. Приведены общие сведения об основных продуктах, получаемых в ходе переработки ЛАО, способах получения и областях их применения. Кратко рассмотрены существующие технологические процессы получения производных ЛАО и применяемые в них катализаторы. Представлены современные тренды в области переработки ЛАО и перспективные направления усовершенствования существующих технологий, включая разработку новых типов катализаторов. Авторы обзора не претендуют на исчерпывающее или достаточно детальное изложение материала, поскольку основная задача обзора – дать общее представление об основных направлениях переработки ЛАО, используемых в этих процессах катализаторах и современных подходах к их улучшению.</p></abstract><trans-abstract xml:lang="en"><p>Linear alpha olefins (LAO) form a class of chemical compounds that are used in the production of highly marketable products, such as plasticizers, synthetic lubricants, surfactants and (co)polymers with the improved operating characteristics. Since the annual world consumption of LAO derivatives is growing, specialists from research institutes, universities and industrial laboratories become involved in LAO processing. The analysis of scientific literature published in recent ten years revealed the absence of general reviews devoted to LAO processing. This review considers modern trends in the processing of LAO, which contain four and more carbon atoms, to technologically important derivatives. General information on the main products obtained by LAO processing, methods of their production and application fields is reported. The existing technological processes used to obtain LAO derivatives as well as the catalysts employed in the processes are briefly described. The review presents modern trends in LAO processing and promising ways for enhancing the available technologies, particularly the development of new types of catalysts. Authors of the review make no pretence to a comprehensive or detailed presentation of the material; the main aim was to give a general idea of the main directions in LAO processing, the catalysts used in such processes, and the advanced approaches to their improvement.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>альфа-олефины</kwd><kwd>сополимеризация</kwd><kwd>оксосинтез</kwd><kwd>гидроформилирование</kwd><kwd>жирные спирты</kwd><kwd>алкилсульфаты</kwd><kwd>алкилэтоксисульфаты</kwd><kwd>этоксилирование</kwd><kwd>сульфатирование</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Alpha olefins</kwd><kwd>copolymerization</kwd><kwd>oxo-synthesis</kwd><kwd>hydroformylation</kwd><kwd>fatty alcohols</kwd><kwd>alkyl sulfates</kwd><kwd>alkyl ethoxy sulfates</kwd><kwd>ethoxylation</kwd><kwd>sulfation</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">Polyvinyl chloride compositions: US6608142B1 USA.</mixed-citation><mixed-citation xml:lang="en">Polyvinyl chloride compositions: US6608142B1 USA.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Impact modifier compositions for rigid PVC compositions of hydrocarbon rubbers and chlorinated polyethylene: US6849694B2 USA.</mixed-citation><mixed-citation xml:lang="en">Impact modifier compositions for rigid PVC compositions of hydrocarbon rubbers and chlorinated polyethylene: US6849694B2 USA.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Greiner E.C., Inoguchi Y. Chemical economics handbook: linear-alpha olefins, 2010.</mixed-citation><mixed-citation xml:lang="en">Greiner E.C., Inoguchi Y. Chemical economics handbook: linear-alpha olefins, 2010.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Marquis D., Sharman S., House R., Sweeney W. // Journal of the American Oil Chemists Society. 1966. V. 43. № 11. P. 607-614.</mixed-citation><mixed-citation xml:lang="en">Marquis D., Sharman S., House R., Sweeney W. // Journal of the American Oil Chemists Society. 1966. V. 43. № 11. P. 607-614.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Takada H., Ishiwatari R. // Environmental science &amp; technology. 1990. V. 24. № 1. P. 86-91.</mixed-citation><mixed-citation xml:lang="en">Takada H., Ishiwatari R. // Environmental science &amp; technology. 1990. V. 24. № 1. P. 86-91.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Белов Г. // Катализ в промышленности. 2014. № 3. С. 13–19.</mixed-citation><mixed-citation xml:lang="en">Белов Г. // Катализ в промышленности. 2014. № 3. С. 13–19.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Olefin production: US6455648B1 USA.</mixed-citation><mixed-citation xml:lang="en">Olefin production: US6455648B1 USA.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Ethylene oligomerization: EP0537609A EU.</mixed-citation><mixed-citation xml:lang="en">Ethylene oligomerization: EP0537609A EU.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Alpha-olefin production: US3647906A USA.</mixed-citation><mixed-citation xml:lang="en">Alpha-olefin production: US3647906A USA.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Process for preparing linear α-olefins: US4783573A USA.</mixed-citation><mixed-citation xml:lang="en">Process for preparing linear α-olefins: US4783573A USA.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Stache H.W. Anionic Surfactants: Organic Chemistry, 1995.</mixed-citation><mixed-citation xml:lang="en">Stache H.W. Anionic Surfactants: Organic Chemistry, 1995.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Catalytic synthesis of linear alpha olefins: US3472910A USA.</mixed-citation><mixed-citation xml:lang="en">Catalytic synthesis of linear alpha olefins: US3472910A USA.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Process for preparing linear α-olefins: US9896391B2 USA.</mixed-citation><mixed-citation xml:lang="en">Process for preparing linear α-olefins: US9896391B2 USA.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Федоров А., Черкасова Е. // Вестник Казанского технологич. ун-та. 2016. Т. 19. № 7. С. 60–65.</mixed-citation><mixed-citation xml:lang="en">Федоров А., Черкасова Е. // Вестник Казанского технологич. ун-та. 2016. Т. 19. № 7. С. 60–65.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Process for converting paraffins to olefins: US4523045A USA.</mixed-citation><mixed-citation xml:lang="en">Process for converting paraffins to olefins: US4523045A USA.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Dehydrogenation catalyst composition: US4914075A USA.</mixed-citation><mixed-citation xml:lang="en">Dehydrogenation catalyst composition: US4914075A USA.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Jongsomjit B., Kaewkrajang P., Shiono T., Praserthdam P. Supporting effects of silica-supported methylaluminoxane (MAO) with zirconocene catalyst on ethylene/1-olefin copolymerization behaviors for linear low-density polyethylene (LLDPE) production // Industrial &amp; engineering chemistry research. 2004. V. 43. № 24. P. 7959-7963.</mixed-citation><mixed-citation xml:lang="en">Jongsomjit B., Kaewkrajang P., Shiono T., Praserthdam P. Supporting effects of silica-supported methylaluminoxane (MAO) with zirconocene catalyst on ethylene/1-olefin copolymerization behaviors for linear low-density polyethylene (LLDPE) production // Industrial &amp; engineering chemistry research. 2004. V. 43. № 24. P. 7959-7963.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Kaminsky W., Piel C., Scharlach K. // Macromolecular Symposia. Wiley Online Library. 2005, P. 25-34.</mixed-citation><mixed-citation xml:lang="en">Kaminsky W., Piel C., Scharlach K. // Macromolecular Symposia. Wiley Online Library. 2005, P. 25-34.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Al-Malaika S., Peng X. // Polymer degradation and stability. 2007. V. 92. № 12. P. 2136-2149.</mixed-citation><mixed-citation xml:lang="en">Al-Malaika S., Peng X. // Polymer degradation and stability. 2007. V. 92. № 12. P. 2136-2149.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Simanke A.G., Galland G.B., Freitas L., da Jornada J.A.H., Quijada R., Mauler R.S. // Polymer. 1999. V. 40. №. 20. P. 5489-5495.</mixed-citation><mixed-citation xml:lang="en">Simanke A.G., Galland G.B., Freitas L., da Jornada J.A.H., Quijada R., Mauler R.S. // Polymer. 1999. V. 40. №. 20. P. 5489-5495.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Kim J.D., Soares J.B. // Journal of Polymer Science Part A: Polymer Chemistry. 2000. V. 38. № 9. P. 1427-1432.</mixed-citation><mixed-citation xml:lang="en">Kim J.D., Soares J.B. // Journal of Polymer Science Part A: Polymer Chemistry. 2000. V. 38. № 9. P. 1427-1432.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Low density copolymer composition of two ethylene-α-olefin copolymers: US4438238A USA.</mixed-citation><mixed-citation xml:lang="en">Low density copolymer composition of two ethylene-α-olefin copolymers: US4438238A USA.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Spalding M.A., Chatterjee A. Handbook of Industrial Polyethylene and Technology: Definitive Guide to Manufacturing, Properties, Processing, Applications and Markets Set, 2017.</mixed-citation><mixed-citation xml:lang="en">Spalding M.A., Chatterjee A. Handbook of Industrial Polyethylene and Technology: Definitive Guide to Manufacturing, Properties, Processing, Applications and Markets Set, 2017.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Arndt J.-H., Brüll R., Macko T., Garg P., Tacx J. // Polymer. 2018. V. 156. P. 214-221.</mixed-citation><mixed-citation xml:lang="en">Arndt J.-H., Brüll R., Macko T., Garg P., Tacx J. // Polymer. 2018. V. 156. P. 214-221.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">De S.K., White J.R., Limited R.T. Rubber Technologist's Handbook, 2001.</mixed-citation><mixed-citation xml:lang="en">De S.K., White J.R., Limited R.T. Rubber Technologist's Handbook, 2001.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Exxon mobil chemical: [сайт]. URL: https://www.exxonmobilchemical.com/en?ln=productsservices</mixed-citation><mixed-citation xml:lang="en">Exxon mobil chemical: [сайт]. URL: https://www.exxonmobilchemical.com/en?ln=productsservices</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Freeman A., Mantell S.C., Davidson J.H. // Solar energy. 2005. V. 79. № 6. P. 624-637.</mixed-citation><mixed-citation xml:lang="en">Freeman A., Mantell S.C., Davidson J.H. // Solar energy. 2005. V. 79. № 6. P. 624-637.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Polybutene Piping Systems Association: [сайт]. URL: https://www.pbpsa.com/pb-1-properties</mixed-citation><mixed-citation xml:lang="en">Polybutene Piping Systems Association: [сайт]. URL: https://www.pbpsa.com/pb-1-properties</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Проклеенная бумага и ее применение в процессах высокоскоростной переработки или репрографии: RU2202019C2 РФ.</mixed-citation><mixed-citation xml:lang="en">Проклеенная бумага и ее применение в процессах высокоскоростной переработки или репрографии: RU2202019C2 РФ.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Lappin G., Sauer J. Alpha olefins Applications Handbook, 1989.</mixed-citation><mixed-citation xml:lang="en">Lappin G., Sauer J. Alpha olefins Applications Handbook, 1989.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Klaue A., Kruck M., Friederichs N., Bertola F., Wu H., Morbidelli M. // Industrial &amp; Engineering Chemistry Research. 2018. V. 58. № 2. P. 886-896.</mixed-citation><mixed-citation xml:lang="en">Klaue A., Kruck M., Friederichs N., Bertola F., Wu H., Morbidelli M. // Industrial &amp; Engineering Chemistry Research. 2018. V. 58. № 2. P. 886-896.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">McDaniel M.P. // Advances in catalysis. 2010. V. 53 P. 123-606.</mixed-citation><mixed-citation xml:lang="en">McDaniel M.P. // Advances in catalysis. 2010. V. 53 P. 123-606.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Hamielec A.E., Soares J.B. // Polypropylene. 1999. V. 2. P. 446-453.</mixed-citation><mixed-citation xml:lang="en">Hamielec A.E., Soares J.B. // Polypropylene. 1999. V. 2. P. 446-453.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Kaminsky W. // Journal of Polymer Science Part A: Polymer Chemistry. 2004. V. 42. № 16. P. 3911-3921.</mixed-citation><mixed-citation xml:lang="en">Kaminsky W. // Journal of Polymer Science Part A: Polymer Chemistry. 2004. V. 42. № 16. P. 3911-3921.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Jeremic D. // Ullmann's Encyclopedia of Industrial Chemistry. 2000. P. 1-42.</mixed-citation><mixed-citation xml:lang="en">Jeremic D. // Ullmann's Encyclopedia of Industrial Chemistry. 2000. P. 1-42.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Langhauser F., Kerth J., Kersting M., Kölle P., Lilge D., Müller P. // Die Angewandte Makromolekulare Chemie: Applied Macromolecular Chemistry and Physics. 1994. V. 223. № 1. P. 155-164.</mixed-citation><mixed-citation xml:lang="en">Langhauser F., Kerth J., Kersting M., Kölle P., Lilge D., Müller P. // Die Angewandte Makromolekulare Chemie: Applied Macromolecular Chemistry and Physics. 1994. V. 223. № 1. P. 155-164.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Olabisi O., Adewale K. Handbook of Thermoplastics, 1997.</mixed-citation><mixed-citation xml:lang="en">Olabisi O., Adewale K. Handbook of Thermoplastics, 1997.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Olefin polymer and production processes thereof: US6838540B2, USA.</mixed-citation><mixed-citation xml:lang="en">Olefin polymer and production processes thereof: US6838540B2, USA.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Polymerisation catalysts: EP1131361B1 EU.</mixed-citation><mixed-citation xml:lang="en">Polymerisation catalysts: EP1131361B1 EU.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Supported polyolefin catalyst for the (co-)polymerization of ethylene in gas phase: EP0453088A1 EU.</mixed-citation><mixed-citation xml:lang="en">Supported polyolefin catalyst for the (co-)polymerization of ethylene in gas phase: EP0453088A1 EU.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Ushakova T., Starchak E., Krasheninnikov V., Samoilenko A., Ivchenko P., Nifant’ev I., Novokshonova L. // Kinetics and Catalysis. 2012. V. 53. № 1. P. 75-83.</mixed-citation><mixed-citation xml:lang="en">Ushakova T., Starchak E., Krasheninnikov V., Samoilenko A., Ivchenko P., Nifant’ev I., Novokshonova L. // Kinetics and Catalysis. 2012. V. 53. № 1. P. 75-83.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Czaja K., Białek M., Utrata A. // Journal of Polymer Science Part A: Polymer Chemistry. 2004. V. 42. № 10. P. 2512-2519.</mixed-citation><mixed-citation xml:lang="en">Czaja K., Białek M., Utrata A. // Journal of Polymer Science Part A: Polymer Chemistry. 2004. V. 42. № 10. P. 2512-2519.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Fujita T., Kawai K. // Topics in Catalysis. 2014. V. 57. № 10-13. P. 852-877.</mixed-citation><mixed-citation xml:lang="en">Fujita T., Kawai K. // Topics in Catalysis. 2014. V. 57. № 10-13. P. 852-877.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Makio H., Terao H., Iwashita A., Fujita T. // Chemical reviews. 2011. V. 111. № 3. P. 2363-2449.</mixed-citation><mixed-citation xml:lang="en">Makio H., Terao H., Iwashita A., Fujita T. // Chemical reviews. 2011. V. 111. № 3. P. 2363-2449.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Furuyama R., Mitani M., Mohri J.-i., Mori R., Tanaka H., Fujita T. // Macromolecules. 2005. V. 38. № 5. P. 1546-1552.</mixed-citation><mixed-citation xml:lang="en">Furuyama R., Mitani M., Mohri J.-i., Mori R., Tanaka H., Fujita T. // Macromolecules. 2005. V. 38. № 5. P. 1546-1552.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Gagieva S.C., Tuskaev V., Takazova R., Buyanovskaya A., Smirnova O., Bravaya N., Bulychev B. // Russian Chemical Bulletin. 2019. V. 68. № 11. P. 2114-2118.</mixed-citation><mixed-citation xml:lang="en">Gagieva S.C., Tuskaev V., Takazova R., Buyanovskaya A., Smirnova O., Bravaya N., Bulychev B. // Russian Chemical Bulletin. 2019. V. 68. № 11. P. 2114-2118.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Mun T.C. Production of Polyethylene Using Gas Fluidized Bed Reactor // Hydrocarbon Processing. 2003.</mixed-citation><mixed-citation xml:lang="en">Mun T.C. Production of Polyethylene Using Gas Fluidized Bed Reactor // Hydrocarbon Processing. 2003.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Carraher C.E., Craver C.D. Applied polymer science: 21st century, 2000.</mixed-citation><mixed-citation xml:lang="en">Carraher C.E., Craver C.D. Applied polymer science: 21st century, 2000.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Wagner J.D., Lappin G.R., Zietz J.R. Alcohols, Higher Aliphatic, Synthetic Processes // Kirk‐Othmer Encyclopedia of Chemical Technology. 2000.</mixed-citation><mixed-citation xml:lang="en">Wagner J.D., Lappin G.R., Zietz J.R. Alcohols, Higher Aliphatic, Synthetic Processes // Kirk‐Othmer Encyclopedia of Chemical Technology. 2000.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Апостолов С., Бабаш С., Белкина Е., Беренц А. Новый справочник химика и технолога. Сырье и продукты промышленности органических и неорганических веществ. Ч. 2. 2006.</mixed-citation><mixed-citation xml:lang="en">Апостолов С., Бабаш С., Белкина Е., Беренц А. Новый справочник химика и технолога. Сырье и продукты промышленности органических и неорганических веществ. Ч. 2. 2006.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Process for the production of 7-17 C aliphatic alcohols comprises cobalt catalyzed hydroformylation of 3-16C olefins whereby the organic phase is extracted with a water containing liquid: DE10227995A1 Germany.</mixed-citation><mixed-citation xml:lang="en">Process for the production of 7-17 C aliphatic alcohols comprises cobalt catalyzed hydroformylation of 3-16C olefins whereby the organic phase is extracted with a water containing liquid: DE10227995A1 Germany.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Zakzeski J., Lee H.R., Leung Y.L., Bell A.T. // Applied Catalysis A: General. 2010. V. 374. № 1-2. P. 201-212.</mixed-citation><mixed-citation xml:lang="en">Zakzeski J., Lee H.R., Leung Y.L., Bell A.T. // Applied Catalysis A: General. 2010. V. 374. № 1-2. P. 201-212.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Sandee A.J., Reek J.N., Kamer P.C., van Leeuwen P.W. // Journal of the American Chemical Society. 2001. V. 123. № 35. P. 8468-8476.</mixed-citation><mixed-citation xml:lang="en">Sandee A.J., Reek J.N., Kamer P.C., van Leeuwen P.W. // Journal of the American Chemical Society. 2001. V. 123. № 35. P. 8468-8476.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Takahashi K., Yamashita M., Nozaki K. // Journal of the American Chemical Society. 2012. V. 134. № 45. P. 18746-18757.</mixed-citation><mixed-citation xml:lang="en">Takahashi K., Yamashita M., Nozaki K. // Journal of the American Chemical Society. 2012. V. 134. № 45. P. 18746-18757.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Kamer P.C., Van Leeuwen P.W., Reek J.N. // Accounts of chemical research. 2001. V. 34. № 11. P. 895-904.</mixed-citation><mixed-citation xml:lang="en">Kamer P.C., Van Leeuwen P.W., Reek J.N. // Accounts of chemical research. 2001. V. 34. № 11. P. 895-904.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Conley B.L., Pennington-Boggio M.K., Boz E., Williams T.J. // Chemical reviews. 2010. V. 110. № 4. P. 2294-2312.</mixed-citation><mixed-citation xml:lang="en">Conley B.L., Pennington-Boggio M.K., Boz E., Williams T.J. // Chemical reviews. 2010. V. 110. № 4. P. 2294-2312.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Fogg D.E., dos Santos E.N. // Coordination chemistry reviews. 2004. V. 248. № 21-24. P. 2365-2379.</mixed-citation><mixed-citation xml:lang="en">Fogg D.E., dos Santos E.N. // Coordination chemistry reviews. 2004. V. 248. № 21-24. P. 2365-2379.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Torres G.M., Frauenlob R., Franke R., Börner A. // Catalysis Science &amp; Technology. 2015. V. 5. № 1. P. 34-54.</mixed-citation><mixed-citation xml:lang="en">Torres G.M., Frauenlob R., Franke R., Börner A. // Catalysis Science &amp; Technology. 2015. V. 5. № 1. P. 34-54.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Srivastava V.K., Shukla R.S., Bajaj H.C., Jasra R.V. // Applied Catalysis A: General. 2005. V. 282. № 1-2. P. 31-38.</mixed-citation><mixed-citation xml:lang="en">Srivastava V.K., Shukla R.S., Bajaj H.C., Jasra R.V. // Applied Catalysis A: General. 2005. V. 282. № 1-2. P. 31-38.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Wu L., Fleischer I., Jackstell R., Profir I., Franke R., Beller M. // Journal of the American Chemical Society. 2013. V. 135. № 38. P. 14306-14312.</mixed-citation><mixed-citation xml:lang="en">Wu L., Fleischer I., Jackstell R., Profir I., Franke R., Beller M. // Journal of the American Chemical Society. 2013. V. 135. № 38. P. 14306-14312.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Ropartz L.C., Morris R.E., Foster D.F., Cole-Hamilton D.J. // Journal of Molecular Catalysis A: Chemical. 2002. V. 182. P. 99-105.</mixed-citation><mixed-citation xml:lang="en">Ropartz L.C., Morris R.E., Foster D.F., Cole-Hamilton D.J. // Journal of Molecular Catalysis A: Chemical. 2002. V. 182. P. 99-105.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Takahashi K., Nozaki K. // Organic letters. 2014. V. 16. № 22. P. 5846-5849.</mixed-citation><mixed-citation xml:lang="en">Takahashi K., Nozaki K. // Organic letters. 2014. V. 16. № 22. P. 5846-5849.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Konya D., Almeida Leñero K.Q., Drent E. // Organometallics. 2006. V. 25. № 13. P. 3166-3174.</mixed-citation><mixed-citation xml:lang="en">Konya D., Almeida Leñero K.Q., Drent E. // Organometallics. 2006. V. 25. № 13. P. 3166-3174.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Cuny G.D., Buchwald S.L. // Journal of the American Chemical Society. 1993. V. 115. № 5. P. 2066-2068.</mixed-citation><mixed-citation xml:lang="en">Cuny G.D., Buchwald S.L. // Journal of the American Chemical Society. 1993. V. 115. № 5. P. 2066-2068.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Hydroformylation process: US4593127A USA.</mixed-citation><mixed-citation xml:lang="en">Hydroformylation process: US4593127A USA.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Pruett R.L., Smith J.A. // The Journal of Organic Chemistry. 1969. V. 34. № 2. P. 327-330.</mixed-citation><mixed-citation xml:lang="en">Pruett R.L., Smith J.A. // The Journal of Organic Chemistry. 1969. V. 34. № 2. P. 327-330.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Arderne C., Holzapfel C.W., Bredenkamp T. // ChemCatChem. 2016. V. 8. № 6. P. 1084-1093.</mixed-citation><mixed-citation xml:lang="en">Arderne C., Holzapfel C.W., Bredenkamp T. // ChemCatChem. 2016. V. 8. № 6. P. 1084-1093.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Suerbaev K.A., Kudaibergenov N.Z., Vavasori A. // Russian Journal of General Chemistry. 2017. V. 87. № 4. P. 707-712.</mixed-citation><mixed-citation xml:lang="en">Suerbaev K.A., Kudaibergenov N.Z., Vavasori A. // Russian Journal of General Chemistry. 2017. V. 87. № 4. P. 707-712.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Chepaikin E., Bezruchenko A., Suerbaev K.A., Shalmagambetov K. // Petroleum Chemistry. 2006. V. 46. № 2. P. 117-121.</mixed-citation><mixed-citation xml:lang="en">Chepaikin E., Bezruchenko A., Suerbaev K.A., Shalmagambetov K. // Petroleum Chemistry. 2006. V. 46. № 2. P. 117-121.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Akiri S.O., Ojwach S.O. // Catalysts. 2019. V. 9. № 2. P. 143.</mixed-citation><mixed-citation xml:lang="en">Akiri S.O., Ojwach S.O. // Catalysts. 2019. V. 9. № 2. P. 143.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Hydroformylation process: US6331656B1 USA.</mixed-citation><mixed-citation xml:lang="en">Hydroformylation process: US6331656B1 USA.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Hydroformylation: US7405329B2 USA.</mixed-citation><mixed-citation xml:lang="en">Hydroformylation: US7405329B2 USA.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Process for hydroformylation of an olefin: US5105018A USA.</mixed-citation><mixed-citation xml:lang="en">Process for hydroformylation of an olefin: US5105018A USA.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Cornils B., Herrmann W.A., Xu J.-H., Zanthoff H.-W. Catalysis from A to Z: a concise encyclopedia, 2020.</mixed-citation><mixed-citation xml:lang="en">Cornils B., Herrmann W.A., Xu J.-H., Zanthoff H.-W. Catalysis from A to Z: a concise encyclopedia, 2020.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Rosales M., González A., González B., Moratinos C., Pérez H., Urdaneta J., Sánchez-Delgado R.A. // Journal of organometallic chemistry. 2005. V. 690. № 12. P. 3095-3098.</mixed-citation><mixed-citation xml:lang="en">Rosales M., González A., González B., Moratinos C., Pérez H., Urdaneta J., Sánchez-Delgado R.A. // Journal of organometallic chemistry. 2005. V. 690. № 12. P. 3095-3098.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Makado G., Morimoto T., Sugimoto Y., Tsutsumi K., Kagawa N., Kakiuchi K. // Advanced Synthesis &amp; Catalysis. 2010. V. 352. № 2‐3. P. 299-304.</mixed-citation><mixed-citation xml:lang="en">Makado G., Morimoto T., Sugimoto Y., Tsutsumi K., Kagawa N., Kakiuchi K. // Advanced Synthesis &amp; Catalysis. 2010. V. 352. № 2‐3. P. 299-304.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Cowan-Ellsberry C., Belanger S., Dorn P., Dyer S., McAvoy D., Sanderson H., Versteeg D., Ferrer D., Stanton K. // Critical reviews in environmental science and technology. 2014. V. 44. № 17. P. 1893-1993.</mixed-citation><mixed-citation xml:lang="en">Cowan-Ellsberry C., Belanger S., Dorn P., Dyer S., McAvoy D., Sanderson H., Versteeg D., Ferrer D., Stanton K. // Critical reviews in environmental science and technology. 2014. V. 44. № 17. P. 1893-1993.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Hutchinson E., Manchester K.E., Winslow L. // The Journal of Physical Chemistry. 1954. V. 58. № 12. P. 1124-1127.</mixed-citation><mixed-citation xml:lang="en">Hutchinson E., Manchester K.E., Winslow L. // The Journal of Physical Chemistry. 1954. V. 58. № 12. P. 1124-1127.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Penfold J., Thomas R.K., Li P., Petkov J.T., Tucker I., Cox A.R., Hedges N., Webster J.R., Skoda M.W. // Langmuir. 2014. V. 30. № 32. P. 9741-9751.</mixed-citation><mixed-citation xml:lang="en">Penfold J., Thomas R.K., Li P., Petkov J.T., Tucker I., Cox A.R., Hedges N., Webster J.R., Skoda M.W. // Langmuir. 2014. V. 30. № 32. P. 9741-9751.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Kosswig K. Surfactants, Ullmann's Encyclopedia of Industrial Chemistry, 2000.</mixed-citation><mixed-citation xml:lang="en">Kosswig K. Surfactants, Ullmann's Encyclopedia of Industrial Chemistry, 2000.</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Process for the preparation of alkanol alkoxylates: EP0082554B1 EU.</mixed-citation><mixed-citation xml:lang="en">Process for the preparation of alkanol alkoxylates: EP0082554B1 EU.</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Heterogeneous alkoxylation using anion-bound metal oxides: US5136106A USA.</mixed-citation><mixed-citation xml:lang="en">Heterogeneous alkoxylation using anion-bound metal oxides: US5136106A USA.</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Continuous process for producing linear, secondary, aliphatic alcohol ethoxylates: US4927954A USA.</mixed-citation><mixed-citation xml:lang="en">Continuous process for producing linear, secondary, aliphatic alcohol ethoxylates: US4927954A USA.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Di Serio M., Lengo P., Gobetto R., Bruni S., Santacesaria E. // Journal of Molecular Catalysis A: Chemical. 1996. V. 112. № 2. P. 235-251.</mixed-citation><mixed-citation xml:lang="en">Di Serio M., Lengo P., Gobetto R., Bruni S., Santacesaria E. // Journal of Molecular Catalysis A: Chemical. 1996. V. 112. № 2. P. 235-251.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Condensation of alkylene oxides: US3328467A USA.</mixed-citation><mixed-citation xml:lang="en">Condensation of alkylene oxides: US3328467A USA.</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Ethoxylation with strontium bases: US4223164A USA.</mixed-citation><mixed-citation xml:lang="en">Ethoxylation with strontium bases: US4223164A USA.</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Barium oxide/cresylic acid catalyzed ethoxylation: US4210764A USA.</mixed-citation><mixed-citation xml:lang="en">Barium oxide/cresylic acid catalyzed ethoxylation: US4210764A USA.</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Domingo X. Anionic Surfactants: Organic Chemistry: Alcohol and alcohol ether sulfates, 1996.</mixed-citation><mixed-citation xml:lang="en">Domingo X. Anionic Surfactants: Organic Chemistry: Alcohol and alcohol ether sulfates, 1996.</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Integrated system for the continuous production of alcohol sulfates: US3370926A USA.</mixed-citation><mixed-citation xml:lang="en">Integrated system for the continuous production of alcohol sulfates: US3370926A USA.</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Process for the production of alcohol sulfates: US3337601A USA</mixed-citation><mixed-citation xml:lang="en">Process for the production of alcohol sulfates: US3337601A USA</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Ингибирование нарастаний в реакционных сосудах: EA200101220A1 Евразия.</mixed-citation><mixed-citation xml:lang="en">Ингибирование нарастаний в реакционных сосудах: EA200101220A1 Евразия.</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Cox M.F. // Journal of the American Oil Chemists Society. 1989. V. 66. № 11. P. 1637-1646.</mixed-citation><mixed-citation xml:lang="en">Cox M.F. // Journal of the American Oil Chemists Society. 1989. V. 66. № 11. P. 1637-1646.</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>
