A Comprehensive Study of Synthesis and Analysis of Anisotropic Iron Oxide and Oxyhydroxide Nanoparticles / Е. О. Chernova, V. V. Botvin, M. R. Galstenkova [et al.]

Уровень набора: NanomaterialsАльтернативный автор-лицо: Chernova, Е. О., chemical engineer, Research Engineer of Tomsk Polytechnic University, 1997-, Elizaveta Olegovna;Botvin, V. V., chemist, Senior Researcher of Tomsk Polytechnic University, Candidate of chemical sciences, 1991-, Vladimir Viktorovich;Galstenkova, M. R., Mariya Romanovna;Mukhortova, Yu. R., Chemical engineer, Engineer of Tomsk Polytechnic University, 1976-, Yulia Ruslanovna;Vagner, D., Dmitry;Gerasimov, E., Evgeny;Surmeneva, M. A., specialist in the field of material science, engineer-researcher of Tomsk Polytechnic University, Associate Scientist, 1984-, Maria Alexandrovna;Kholkin, A. L., physicist, Director of the International Research Center for PMEM of the Tomsk Polytechnic University, Candidate of Physical and Mathematical Sciences, 1954-, Andrei Leonidovich;Surmenev, R. A., physicist, Associate Professor of Tomsk Polytechnic University, Senior researcher, Candidate of physical and mathematical sciences, 1982-, Roman AnatolievichКоллективный автор (вторичный): Национальный исследовательский Томский политехнический университет, Исследовательская школа химических и биомедицинских технологий, Международный научно-исследовательский центр "Пьезо- и магнитоэлектрические материалы";Национальный исследовательский Томский политехнический университет, Исследовательская школа химических и биомедицинских технологий, (2017- )Язык: английский.Страна: .Резюме или реферат: One-dimensional anisotropic nanoparticles are of great research interest across a wide range of biomedical applications due to their specific physicochemical and magnetic properties in comparison with isotropic magnetic nanoparticles. In this work, the formation of iron oxides and oxyhydroxide anisotropic nanoparticles (ANPs) obtained by the co-precipitation method in the presence of urea was studied. Reaction pathways of iron oxide and oxyhydroxide ANPs formation are described based on of X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and pulse magnetometry studies. It is shown that a nonmonotonic change in the Fe3O4 content occurs during synthesis. The maximum content of the Fe3O4 phase of 47.4% was obtained at 12 h of the synthesis. At the same time, the reaction products contain ANPs of a-FeOOH and submicron isotropic particles of Fe3O4, the latter formation can occur due to the oxidation of Fe2+ ions by air-oxygen and Ostwald ripening processes. A subsequent increase in the synthesis time leads to the predominant formation of an a-FeOOH phase due to the oxidation of Fe3O4. As a result of the work, a methodological scheme for the analysis of iron oxide and oxyhydroxide ANPs was developed..Примечания о наличии в документе библиографии/указателя: [References: 72 tit.].Тематика: электронный ресурс | труды учёных ТПУ | iron oxides | magnetite | anisotropic nanoparticles | co-precipitation | methodological scheme | оксиды железа | магнетит | наночастицы Ресурсы он-лайн:Щелкните здесь для доступа в онлайн
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[References: 72 tit.]

One-dimensional anisotropic nanoparticles are of great research interest across a wide range of biomedical applications due to their specific physicochemical and magnetic properties in comparison with isotropic magnetic nanoparticles. In this work, the formation of iron oxides and oxyhydroxide anisotropic nanoparticles (ANPs) obtained by the co-precipitation method in the presence of urea was studied. Reaction pathways of iron oxide and oxyhydroxide ANPs formation are described based on of X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and pulse magnetometry studies. It is shown that a nonmonotonic change in the Fe3O4 content occurs during synthesis. The maximum content of the Fe3O4 phase of 47.4% was obtained at 12 h of the synthesis. At the same time, the reaction products contain ANPs of a-FeOOH and submicron isotropic particles of Fe3O4, the latter formation can occur due to the oxidation of Fe2+ ions by air-oxygen and Ostwald ripening processes. A subsequent increase in the synthesis time leads to the predominant formation of an a-FeOOH phase due to the oxidation of Fe3O4. As a result of the work, a methodological scheme for the analysis of iron oxide and oxyhydroxide ANPs was developed.

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