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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">kemsu</journal-id><journal-title-group><journal-title xml:lang="ru">СибСкрипт</journal-title><trans-title-group xml:lang="en"><trans-title>SibScript</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2949-2122</issn><issn pub-type="epub">2949-2092</issn><publisher><publisher-name>Kemerovo State University</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">kemsu-279</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>Химия</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHEMISTRY</subject></subj-group></article-categories><title-group><article-title>К ВОПРОСУ О МЕХАНИЗМЕ ОБРАЗОВАНИЯ N2O В КАТАЛИЗИРУЕМОЙ РЕАКЦИИ МЕЖДУ ГИДРОКСИЛАММОНИЕМ И НИТРИТОМ В ВОДЕ, ЭТИЛЕНГЛИКОЛЕ И ДИОКСАНЕ</article-title><trans-title-group xml:lang="en"><trans-title>ABOUT THE MECHANISM FOR N2O FORMATION IN CATALYZED REACTION BETWEEN HYDROXYLAMMONIUM AND NITRITE IN WATER, ETHYLENE GLYCOL AND DIOXANE</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>Башмаков</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Bashmakov</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Башмаков Александр Сергеевич – кандидат физико-математических наук, доцент кафедры физической, коллоидной, аналитической и органической химии</p></bio><bio xml:lang="en"><p>Alexander S. Bashmakov – Candidate of Physics and Mathematics, Assistant Professor at the Department of Physical, Colloidal, Analytical and Organic Chemistry</p></bio><email xlink:type="simple">b2techcomp@rambler.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>Дягилева</surname><given-names>Е. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Dyagileva</surname><given-names>E. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дягилева Елена Павловна – кандидат химических наук, доцент кафедры физической, коллоидной, аналитической и органической химии</p></bio><bio xml:lang="en"><p>Elena P. Dyagileva – Candidate of Chemistry, Assistant Professor at the Department of Physical, Colloidal, Analytical and Organic Chemistry</p></bio><email xlink:type="simple">dyagilevaep@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>Кургачев</surname><given-names>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kurgachev</surname><given-names>D. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кургачев Дмитрий Андреевич – интерн кафедры фармацевтической химии</p></bio><bio xml:lang="en"><p>Dmitriy A. Kurgachev – Intern at the Department Pharmaceutical Chemistry</p></bio><email xlink:type="simple">Daemond91@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>Леонтьева</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Leonteva</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Леонтьева Елена Валерьевна – кандидат химических наук, доцент кафедры физической, коллоидной, аналитической и органической химии</p></bio><bio xml:lang="en"><p>Elena V. Leonteva – Candidate of Chemistry, Assistant Professor at the Department of Physical, Colloidal, Analytical and Organic Chemistry</p></bio><email xlink:type="simple">elena_leonteva@list.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Кемеровская государственная медицинская академия<country>Россия</country></aff><aff xml:lang="en">Kemerovo State Medical Academy<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2015</year></pub-date><pub-date pub-type="epub"><day>27</day><month>02</month><year>2016</year></pub-date><volume>0</volume><issue>4-3</issue><fpage>228</fpage><lpage>232</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Башмаков А.С., Дягилева Е.П., Кургачев Д.А., Леонтьева Е.В., 2015</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="ru">Башмаков А.С., Дягилева Е.П., Кургачев Д.А., Леонтьева Е.В.</copyright-holder><copyright-holder xml:lang="en">Bashmakov A.S., Dyagileva E.P., Kurgachev D.A., Leonteva E.V.</copyright-holder><license 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.sibscript.ru/jour/article/view/279">https://www.sibscript.ru/jour/article/view/279</self-uri><abstract><p>Газообразный продукт реакции между гидроксиламмонием и нитритом в этиленгликоле, диоксане, смеси этиленгликоль – диоксан идентифицирован как N2O. Показано, что эта реакция катализируется борной кислотой и ионами меди. Представлен механизм образования N2O в воде и органических растворителях. Полученные результаты позволяют оптимизировать условия получения N2O из солей гидроксиламмония и увеличить его выход.</p></abstract><trans-abstract xml:lang="en"><p>The gaseous product of the reaction between hydroxylammonium and nitrite in ethylene glycol, dioxane and ethylene glycol-dioxane mixture was identified as N2O. It was shown that this reaction is catalyzed by boron acid and copper ions. The mechanism for N2O formation and the influence of copper ions on it in water and organic solvents is discussed. The obtained results allow optimizing the conditions of obtaining N2O from hydroxylammonium salts and increasing its yield.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гидроксиламин</kwd><kwd>гидроксиламмоний</kwd><kwd>нитрит</kwd><kwd>азотистая кислота</kwd><kwd>азотноватистая кислота</kwd><kwd>оксид азота (I)</kwd><kwd>катализ ионами меди</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hydroxylamine</kwd><kwd>hydroxylammonium</kwd><kwd>nitrite</kwd><kwd>nitrous acid</kwd><kwd>hyponitrous acid</kwd><kwd>nitrogen oxide (I)</kwd><kwd>catalysis by copper ions</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">Audrieth L. F. Parallelism in the decomposition of ammonium, hydrazine, and hydroxylammonium nitrites. Hyponitrous acid as a hydroxylamino-nitrous acid // J. Phys. Chem. 1930. V. 34. № 3. P. 538 – 542.</mixed-citation><mixed-citation xml:lang="en">Audrieth L. F. 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