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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">najo</journal-id><journal-title-group><journal-title xml:lang="en">Nanosystems: Physics, Chemistry, Mathematics</journal-title><trans-title-group xml:lang="ru"><trans-title>Наносистемы: физика, химия, математика</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2220-8054</issn><issn pub-type="epub">2305-7971</issn><publisher><publisher-name>Университет ИТМО</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17586/2220-8054-2016-7-1-234-243</article-id><article-id custom-type="elpub" pub-id-type="custom">najo-985</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="en"><subject>PAPERS, PRESENTED AT THE CONFERENCE</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>PAPERS, PRESENTED AT THE CONFERENCE</subject></subj-group></article-categories><title-group><article-title>Reactivity in combustion process for expanded graphites: influence of dimensional effect</article-title><trans-title-group xml:lang="ru"><trans-title>Reactivity in combustion process for expanded graphites: influence of dimensional effect</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>Logvinenko</surname><given-names>V. A.</given-names></name><name name-style="western" xml:lang="en"><surname>Logvinenko</surname><given-names>V. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Novosibirsk 630090</p></bio><bio xml:lang="en"><p>Novosibirsk 630090</p></bio><email xlink:type="simple">val@niic.nsc.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>Makotchenko</surname><given-names>V. G.</given-names></name><name name-style="western" xml:lang="en"><surname>Makotchenko</surname><given-names>V. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Novosibirsk 630090</p></bio><bio xml:lang="en"><p>Novosibirsk 630090</p></bio><email xlink:type="simple">mwg@niic.nsc.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Fedorov</surname><given-names>V. E.</given-names></name><name name-style="western" xml:lang="en"><surname>Fedorov</surname><given-names>V. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Novosibirsk 630090</p></bio><bio xml:lang="en"><p>Novosibirsk 630090</p></bio><email xlink:type="simple">fed@niic.nsc.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University</institution></aff><aff xml:lang="en"><institution>Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State University</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences</institution></aff><aff xml:lang="en"><institution>Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>14</day><month>08</month><year>2025</year></pub-date><volume>7</volume><issue>1</issue><issue-title>Special Issue: Proceedings of the 12th Biennial International Conference “Advanced Carbon Nanostructures” (ACNS’2015)</issue-title><fpage>234</fpage><lpage>243</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Logvinenko V.A., Makotchenko V.G., Fedorov V.E., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Logvinenko V.A., Makotchenko V.G., Fedorov V.E.</copyright-holder><copyright-holder xml:lang="en">Logvinenko V.A., Makotchenko V.G., Fedorov V.E.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" 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://nanojournal.ifmo.ru/jour/article/view/985">https://nanojournal.ifmo.ru/jour/article/view/985</self-uri><abstract><p>Thermal stability in combustion reaction for natural graphite, graphene and several expanded graphite phases were studied; the kinetic parameters of the oxidation reaction were calculated for two samples. Natural graphite (crystalline particles 200 – 300 µm) has the maximum stability (E1 = 201 ± 2 kJ/mol, lg A1 = 7.1 ± 0.1), while multilayer graphene is the most reactive (E2 = 120 ± 1 kJ mol−1, lg A2 = 4.3 ± 0.10). The different sample grain sizes and their different structures result in different thermal stabilities: both in the reaction zones location (i.e. in the topochemical equation forms), and in the kinetic parameters’ values.</p></abstract><trans-abstract xml:lang="ru"><p>Thermal stability in combustion reaction for natural graphite, graphene and several expanded graphite phases were studied; the kinetic parameters of the oxidation reaction were calculated for two samples. Natural graphite (crystalline particles 200 – 300 µm) has the maximum stability (E1 = 201 ± 2 kJ/mol, lg A1 = 7.1 ± 0.1), while multilayer graphene is the most reactive (E2 = 120 ± 1 kJ mol−1, lg A2 = 4.3 ± 0.10). The different sample grain sizes and their different structures result in different thermal stabilities: both in the reaction zones location (i.e. in the topochemical equation forms), and in the kinetic parameters’ values.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>natural graphite</kwd><kwd>graphene</kwd><kwd>expanded graphite</kwd><kwd>thermal stability</kwd><kwd>non-isothermal kinetics</kwd><kwd>combustion</kwd></kwd-group><kwd-group xml:lang="en"><kwd>natural graphite</kwd><kwd>graphene</kwd><kwd>expanded graphite</kwd><kwd>thermal stability</kwd><kwd>non-isothermal kinetics</kwd><kwd>combustion</kwd></kwd-group><funding-group><funding-statement xml:lang="en">The work was supported by the Russian Scientific Foundation, Project 14-13-00674.</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">Buffat Ph., Borel J.P. Size effect on the melting temperature of gold particles. Phys. Rev., 1976, A 13, P. 2287–2298.</mixed-citation><mixed-citation xml:lang="en">Buffat Ph., Borel J.P. Size effect on the melting temperature of gold particles. Phys. Rev., 1976, A 13, P. 2287–2298.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Lai S.L., Carlsson J.R.A., Allen L.H. Melting point depression of Al clusters generated during the early stages of film growth: Nanocalorimetry measurements. Appl. Phys. Lett., 1998, 72, P. 1098–1100.</mixed-citation><mixed-citation xml:lang="en">Lai S.L., Carlsson J.R.A., Allen L.H. Melting point depression of Al clusters generated during the early stages of film growth: Nanocalorimetry measurements. Appl. Phys. Lett., 1998, 72, P. 1098–1100.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Bulavchenko A.I., Demidova M.G., Podlipskaya T.Yu., Tatarchuk V.V., Druzhinina I.A. Alekseev A.V., Logvinenko V.A., Drebushchak V.A. Microemulstion synthesis of powders of water soluble energy saturated salts. Russ. J. Inorg. Chem., 2012, 57(6), P. 769–776.</mixed-citation><mixed-citation xml:lang="en">Bulavchenko A.I., Demidova M.G., Podlipskaya T.Yu., Tatarchuk V.V., Druzhinina I.A. Alekseev A.V., Logvinenko V.A., Drebushchak V.A. Microemulstion synthesis of powders of water soluble energy saturated salts. Russ. J. Inorg. Chem., 2012, 57(6), P. 769–776.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Yusupov T.S., Shumskaya L.G., Burdukov A.P., Logvinenko V.A. Reactivity of coal of different stages of metamorphism in the processes of thermo-oxidative destruction. Chemistry for Sustainable Development, 2011, 19, P. 389–394.</mixed-citation><mixed-citation xml:lang="en">Yusupov T.S., Shumskaya L.G., Burdukov A.P., Logvinenko V.A. Reactivity of coal of different stages of metamorphism in the processes of thermo-oxidative destruction. Chemistry for Sustainable Development, 2011, 19, P. 389–394.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Backreedy R., Jones J.M., Pourkashanian M., Williams A. A study of the reaction of oxygen with graphite : Model chemistry. Faraday Discuss., 2001, 119, P. 385–394.</mixed-citation><mixed-citation xml:lang="en">Backreedy R., Jones J.M., Pourkashanian M., Williams A. A study of the reaction of oxygen with graphite : Model chemistry. Faraday Discuss., 2001, 119, P. 385–394.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Bews I.M., Hayhurst A.N., Richardson S.M, Taylor S.G. The order, Arrhenius parameters, and mechanism of the reaction between gaseous oxygen and solid carbon. Combust. Flame, 2001, 124, P. 231–245.</mixed-citation><mixed-citation xml:lang="en">Bews I.M., Hayhurst A.N., Richardson S.M, Taylor S.G. The order, Arrhenius parameters, and mechanism of the reaction between gaseous oxygen and solid carbon. Combust. Flame, 2001, 124, P. 231–245.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Jianga W., Nadeaub G., Zaghibb K., Kinoshitaa K. Thermal analysis of the oxidation of natural graphite – effect of particle size. Thermoch. Acta, 2000, 351, P. 85–93.</mixed-citation><mixed-citation xml:lang="en">Jianga W., Nadeaub G., Zaghibb K., Kinoshitaa K. Thermal analysis of the oxidation of natural graphite – effect of particle size. Thermoch. Acta, 2000, 351, P. 85–93.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Makotchenko V.G., Grayfer E.D., Nazarov A.S., Kim S.-J., Fedorov V.E. The synthesis and properties of highly exfoliated graphites from fluorinated graphite intercalation compounds. Carbon, 2011, 49(10), P. 3233–3241.</mixed-citation><mixed-citation xml:lang="en">Makotchenko V.G., Grayfer E.D., Nazarov A.S., Kim S.-J., Fedorov V.E. The synthesis and properties of highly exfoliated graphites from fluorinated graphite intercalation compounds. Carbon, 2011, 49(10), P. 3233–3241.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Hummers Jr.W.S., Offeman R.E. Preparation of graphitic oxide. J. Am. Chem. Soc., 1958, 80(6), P. 1339.</mixed-citation><mixed-citation xml:lang="en">Hummers Jr.W.S., Offeman R.E. Preparation of graphitic oxide. J. Am. Chem. Soc., 1958, 80(6), P. 1339.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Rudorff W., Hofmann U. Uber Graphitsaltse. Z. Anorg. Allg. Chem. B, 1938, 238(1), P. 1–50.</mixed-citation><mixed-citation xml:lang="en">Rudorff W., Hofmann U. Uber Graphitsaltse. Z. Anorg. Allg. Chem. B, 1938, 238(1), P. 1–50.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Metrot A., Fisher J.E. Charge-transfer reactions during anodic oxidation of graphite in H2SO4. Synth. Met., 1981, 3, P. 201–207.</mixed-citation><mixed-citation xml:lang="en">Metrot A., Fisher J.E. Charge-transfer reactions during anodic oxidation of graphite in H2SO4. Synth. Met., 1981, 3, P. 201–207.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Avdeev V.V., Monyakina L.A., Nikolskaya I.V., Sorokina N.E., Semenenko K.N. The choice of oxidizers for graphite hydrogen sulfate chemical synthesis. Carbon, 1992, 30(6), P. 819–824.</mixed-citation><mixed-citation xml:lang="en">Avdeev V.V., Monyakina L.A., Nikolskaya I.V., Sorokina N.E., Semenenko K.N. The choice of oxidizers for graphite hydrogen sulfate chemical synthesis. Carbon, 1992, 30(6), P. 819–824.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Scherrer P. Bestimmung der Grösse und der Inneren Struktur von Kolloidteilchen Mittels Röntgenstrahlen, Nachrichten von der Gesellschaft der Wissenschaften, Göttingen. Mathematisch-Physikalische Klasse, 1918, 2, P. 98–100.</mixed-citation><mixed-citation xml:lang="en">Scherrer P. Bestimmung der Grösse und der Inneren Struktur von Kolloidteilchen Mittels Röntgenstrahlen, Nachrichten von der Gesellschaft der Wissenschaften, Göttingen. Mathematisch-Physikalische Klasse, 1918, 2, P. 98–100.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Netzsch Thermokinetics. http://www.netzsch-thermal-analysis.com/us/products-%20%20solutions/advanced-software/thermokinetics.html</mixed-citation><mixed-citation xml:lang="en">Netzsch Thermokinetics. http://www.netzsch-thermal-analysis.com/us/products-%20%20solutions/advanced-software/thermokinetics.html</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Moukhina E. Determination of kinetic mechanisms for reactions measured with thermoanalytical instruments. J. Therm. Anal. Calorim., 2012, 109, P. 1203–1214.</mixed-citation><mixed-citation xml:lang="en">Moukhina E. Determination of kinetic mechanisms for reactions measured with thermoanalytical instruments. J. Therm. Anal. Calorim., 2012, 109, P. 1203–1214.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Kissinger H.E. Reaction kinetics in differential thermal analysis. Anal. Chem., 1957, 29, P. 1702–1706.</mixed-citation><mixed-citation xml:lang="en">Kissinger H.E. Reaction kinetics in differential thermal analysis. Anal. Chem., 1957, 29, P. 1702–1706.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Friedman H.L. Kinetics of thermal degradation of char-forming plastics from thermogravimetry. J. Polym. Sci., 1963, 6, P. 183–195.</mixed-citation><mixed-citation xml:lang="en">Friedman H.L. Kinetics of thermal degradation of char-forming plastics from thermogravimetry. J. Polym. Sci., 1963, 6, P. 183–195.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Ozawa T. A new method of analyzing thermogravimetric data. Bull. Chem. Soc. Japan, 1965, 38, P. 1881–1886.</mixed-citation><mixed-citation xml:lang="en">Ozawa T. A new method of analyzing thermogravimetric data. Bull. Chem. Soc. Japan, 1965, 38, P. 1881–1886.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Ozawa T. Estimation of activation energy by isoconversion methods. Thermochim. Acta, 1992, 203, P. 159– 165.</mixed-citation><mixed-citation xml:lang="en">Ozawa T. Estimation of activation energy by isoconversion methods. Thermochim. Acta, 1992, 203, P. 159– 165.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Flynn J.H., Wall L.A. General treatment of the thermogravimetry of polymers. J. Res. Nat. Bur. Stand., 1966, 70, P. 478–523.</mixed-citation><mixed-citation xml:lang="en">Flynn J.H., Wall L.A. General treatment of the thermogravimetry of polymers. J. Res. Nat. Bur. Stand., 1966, 70, P. 478–523.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Opfermann J., Kaisersberger E. An advantageous variant of the Ozawa-Flynn-Wall analysis. Thermochim. Acta, 1992, 203, P. 167–175.</mixed-citation><mixed-citation xml:lang="en">Opfermann J., Kaisersberger E. An advantageous variant of the Ozawa-Flynn-Wall analysis. Thermochim. Acta, 1992, 203, P. 167–175.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Opfermann J.R., Kaisersberger E., Flammersheim H.J. Model-free analysis of thermo-analytical data - advantages and limitations. Thermochim. Acta, 2002, 391, P. 119–127.</mixed-citation><mixed-citation xml:lang="en">Opfermann J.R., Kaisersberger E., Flammersheim H.J. Model-free analysis of thermo-analytical data - advantages and limitations. Thermochim. Acta, 2002, 391, P. 119–127.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Vyazovkin S. Model-free kinetics: staying free of multiplying entities without necessity. J. Therm. Anal. Calorim., 2006, 83, P. 45–51.</mixed-citation><mixed-citation xml:lang="en">Vyazovkin S. Model-free kinetics: staying free of multiplying entities without necessity. J. Therm. Anal. Calorim., 2006, 83, P. 45–51.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Simon P. Single-step kinetics approximation employing non-Arrhenius temperature functions. J. Therm. Anal. Calorim., 2005, 79, P. 703–708.</mixed-citation><mixed-citation xml:lang="en">Simon P. Single-step kinetics approximation employing non-Arrhenius temperature functions. J. Therm. Anal. Calorim., 2005, 79, P. 703–708.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Simon P. The single-step approximation: attributes, strong and weak sides. J. Therm. Anal. Calorim., 2007, 88, P. 709–715.</mixed-citation><mixed-citation xml:lang="en">Simon P. The single-step approximation: attributes, strong and weak sides. J. Therm. Anal. Calorim., 2007, 88, P. 709–715.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Borchard H.J., Daniels F. The application of differential thermal analysis to the study of reaction kinetics. J. Amer. Chem. Soc., 1957, 79, P. 41–46.</mixed-citation><mixed-citation xml:lang="en">Borchard H.J., Daniels F. The application of differential thermal analysis to the study of reaction kinetics. J. Amer. Chem. Soc., 1957, 79, P. 41–46.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Vyazovkin S., Burnham A.K., Criado J.M., Luis A., Perez-Maqueda L.A., Popescu C., Sbirrazzuoli N. ICTAC Kinetics Committee recommendations for performing kinetic computations on thermal analysis data. Thermochim. Acta, 2011, 520, P. 1–19.</mixed-citation><mixed-citation xml:lang="en">Vyazovkin S., Burnham A.K., Criado J.M., Luis A., Perez-Maqueda L.A., Popescu C., Sbirrazzuoli N. ICTAC Kinetics Committee recommendations for performing kinetic computations on thermal analysis data. Thermochim. Acta, 2011, 520, P. 1–19.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Vyazovkin S., Chrissafis K., Di Lorenzo M.L., Koga N., Pijolat M., Roduit B., Sbirrazzuoli N., Sun˜ol J.J. ICTAC Kinetics Committee recommendations for collecting experimental thermal analysis data for kinetic computations. Thermochim. Acta, 2014, 590, P. 1–23.</mixed-citation><mixed-citation xml:lang="en">Vyazovkin S., Chrissafis K., Di Lorenzo M.L., Koga N., Pijolat M., Roduit B., Sbirrazzuoli N., Sun˜ol J.J. ICTAC Kinetics Committee recommendations for collecting experimental thermal analysis data for kinetic computations. Thermochim. Acta, 2014, 590, P. 1–23.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Simon P., Thomas P., Dubaj T., Cibulkova Z., Peller A., Veverka M. The mathematical incorrectness of the integral isoconversional methods in case of variable activation energy and the consequences. J. Therm. Anal. Calorim., 2014, 115, P. 853–859.</mixed-citation><mixed-citation xml:lang="en">Simon P., Thomas P., Dubaj T., Cibulkova Z., Peller A., Veverka M. The mathematical incorrectness of the integral isoconversional methods in case of variable activation energy and the consequences. J. Therm. Anal. Calorim., 2014, 115, P. 853–859.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Sestak J. Is the original Kissinger equation obsolete today: not obsolete the entire non-isothermal kinetics? J. Therm. Anal. Calorim., 2014, 117, P. 3–7.</mixed-citation><mixed-citation xml:lang="en">Sestak J. Is the original Kissinger equation obsolete today: not obsolete the entire non-isothermal kinetics? J. Therm. Anal. Calorim., 2014, 117, P. 3–7.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Logvinenko V. Stability and reactivity of coordination and inclusion compounds in the reversible processes of thermal dissociation. Thermochim. Acta, 1999, 340-341, P. 293–299.</mixed-citation><mixed-citation xml:lang="en">Logvinenko V. Stability and reactivity of coordination and inclusion compounds in the reversible processes of thermal dissociation. Thermochim. Acta, 1999, 340-341, P. 293–299.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Logvinenko V. Solid state coordination chemistry. The quantitative thermoanalytical study of thermal dissociation reactions. J. Therm. Anal. Calorim., 2000, 60, P. 9–15.</mixed-citation><mixed-citation xml:lang="en">Logvinenko V. Solid state coordination chemistry. The quantitative thermoanalytical study of thermal dissociation reactions. J. Therm. Anal. Calorim., 2000, 60, P. 9–15.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Logvinenko V. Stability of supramolecular compounds under heating. Thermodynamic and kinetic aspects. J. Therm. Anal. Calorim., 2010, 101, P. 577–583.</mixed-citation><mixed-citation xml:lang="en">Logvinenko V. Stability of supramolecular compounds under heating. Thermodynamic and kinetic aspects. J. Therm. Anal. Calorim., 2010, 101, P. 577–583.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Logvinenko V., Drebushchak V., Pinakov D., Chekhova G. Thermodynamic and kinetic stability of inclusion compounds under heating. J. Therm. Anal. Calorim., 2007, 90, P. 23–30.</mixed-citation><mixed-citation xml:lang="en">Logvinenko V., Drebushchak V., Pinakov D., Chekhova G. Thermodynamic and kinetic stability of inclusion compounds under heating. J. Therm. Anal. Calorim., 2007, 90, P. 23–30.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Ginak A.Y., Dimshits V.A., Rosovskiy A.Ya. Kinetics of the anisotropic reactions. Part I. Theoretical model. Kinetika i katalis, 1989, 30, P. 83–91 (in Russian).</mixed-citation><mixed-citation xml:lang="en">Ginak A.Y., Dimshits V.A., Rosovskiy A.Ya. Kinetics of the anisotropic reactions. Part I. Theoretical model. Kinetika i katalis, 1989, 30, P. 83–91 (in Russian).</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>
