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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">10.17586/2220-8054-2025-16-4-472-482</article-id><article-id custom-type="elpub" pub-id-type="custom">najo-1447</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>CHEMISTRY AND MATERIALS SCIENCE</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ХИМИЯ И НАУКА О МАТЕРИАЛАХ</subject></subj-group></article-categories><title-group><article-title>Phase formation in the BiPO4–YPO4–(H2O) system</article-title><trans-title-group xml:lang="ru"><trans-title>Фазообразование в системе BiPO4–YPO4–(H2O)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0008-8804-4732</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Осминина</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Osminina</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="en"><p>Alena A. Osminina </p><p>St. Petersburg</p></bio><email xlink:type="simple">alenaosminina3001@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4345-6086</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Еловиков</surname><given-names>Д. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Elovikov</surname><given-names>D. P.</given-names></name></name-alternatives><bio xml:lang="en"><p>Dmitry P. Elovikov</p><p>St. Petersburg</p></bio><email xlink:type="simple">syncdima@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2807-375X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Проскурина</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Proskurina</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="en"><p>Olga V. Proskurina </p><p>St. Petersburg</p></bio><email xlink:type="simple">proskurinaov@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="en">Branch of Petersburg Nuclear Physics Institute named by B. P. Konstantinov of National Research Centre “Kurchatov Institute” – Institute of Silicate Chemistry;&#13;
Ioffe Institute;&#13;
St. Petersburg State Institute of Technology<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="en">Branch of Petersburg Nuclear Physics Institute named by B. P. Konstantinov of National Research Centre “Kurchatov Institute” – Institute of Silicate Chemistry;&#13;
St. Petersburg Electrotechnical University “LETI”<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="en">Ioffe Institute;&#13;
St. Petersburg State Institute of Technology<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>03</day><month>09</month><year>2025</year></pub-date><volume>16</volume><issue>4</issue><fpage>472</fpage><lpage>482</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Osminina A.A., Elovikov D.P., Proskurina O.V., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Осминина А.А., Еловиков Д.П., Проскурина О.В.</copyright-holder><copyright-holder xml:lang="en">Osminina A.A., Elovikov D.P., Proskurina O.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://nanojournal.ifmo.ru/jour/article/view/1447">https://nanojournal.ifmo.ru/jour/article/view/1447</self-uri><abstract><p>This work is devoted to the study of phase equilibria in the BiPO4–YPO4–(nH2O) system under mild conditions. It was shown that using the precipitation method leads to crystallization of the samples into the rhabdophane phase YPO4 · nH2O and the ximengite phase BiPO4. Hydrothermal treatment of the samples at 160◦C results in the gradual transformation of hexagonal yttrium phosphate with a rhabdophane-type structure into tetragonal xenotime YPO4, and hexagonal bismuth phosphate with a ximengite-type structure into monoclinic bismuth phosphate (space group P 21/n). The transformation into the stable phases of xenotime and monoclinic bismuth phosphate is almost complete after 28 days of isothermal holding under hydrothermal conditions at 160◦C. Moreover, the lower the content of the second component in samples containing both Bi and Y, the faster the structural transformation into the stable phase proceeds. A solid solution based on monoclinic bismuth phosphate with the composition Bi0.94Y0.06PO4 is formed in the system. Before disappearing, the rhabdophane-type phase represents a solid solution with the composition Y0.8Bi0.2PO4 · nH2O. The crystallite sizes of all phases increase with an increase in the bismuth content in the system.</p></abstract><trans-abstract xml:lang="ru"><sec><title>Работа посвящена изучению фазовых равновесий в системе BiPO4-YPO4-(nH2O) в мягких условиях. Показано, что при использовании метода осаждения образцы кристаллизуются в фазах рабдофана YPO4·nH2O и ксименгита BiPO4. Гидротермальная обработка образцов при 160°C приводит к постепенной трансформации гексагонального фосфата иттрия со структурой рабдофана в тетрагональный ксенотим YPO4 и гексагонального фосфата висмута со структурой ксименгита в моноклинный фосфат висмута (P21/n). Трансформация в устойчивые фазы ксенотима и моноклинного фосфата висмута завершается практически полностью через 28 дней изотермической выдержки в гидротермальных условиях при 160°C. Причем, чем меньше второго компонента в образцах, содержащих как Bi, так и Y, тем быстрее идет процесс структурной трансформации в устойчивую фазу. В системе формируется твёрдый раствор на основе моноклинного фосфата висмута состава Bi0,94Y0,06PO4. Фаза со структурой рабдофана перед исчезновением представляет собой твердый раствор состава Y0,8Bi0,2PO4·nH2O. Размеры кристаллитов всех фаз возрастают с увеличением доли висмута в системе</title></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>нанокристаллы</kwd><kwd>фазообразование</kwd><kwd>фосфат висмута</kwd><kwd>ортофосфат иттрия</kwd><kwd>гидротермальный синтез</kwd></kwd-group><kwd-group xml:lang="en"><kwd>nanocrystals</kwd><kwd>phase formation</kwd><kwd>bismuth phosphate</kwd><kwd>yttrium orthophosphate</kwd><kwd>hydrothermal synthesis</kwd></kwd-group><funding-group xml:lang="en"><funding-statement>The authors are grateful to Corresponding Member of the Russian Academy of Sciences V. V. Gusarov for his attention to the work and valuable comments, as well as D. P. Danilovich for his help in conducting the research. The work of A. A. O. and D. P. E. was carried out with the support of the Russian Science Foundation project No. 24-13-00445. Scanning electron microscopy and elemental analyses of samples were performed employing the equipment of the Engineering Center of the St. Petersburg State Institute of Technology. X-ray diffraction studies were carried out using the DRON-8 diffractometer in the laboratory of new inorganic materials (Ioffe Institute).</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">Sankar S., RajA.N., Jyothi C.K., Warrier K.G.K., Padmanabhan P.V.A. Room temperature synthesis of high temperature stable lanthanum phosphate-yttria nanocomposite. 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