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Co-Precipitation of Fe—Cu Bimetal Oxalates in an Aqueous Solution and Their Thermally Induced Decomposition

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F21%3A73607917" target="_blank" >RIV/61989592:15310/21:73607917 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/ejic.202100581" target="_blank" >https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/ejic.202100581</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/ejic.202100581" target="_blank" >10.1002/ejic.202100581</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Co-Precipitation of Fe—Cu Bimetal Oxalates in an Aqueous Solution and Their Thermally Induced Decomposition

  • Popis výsledku v původním jazyce

    This work focuses on the preparation of bimetal Fe−Cu oxalates by a co-precipitation reaction in an aqueous solution and subsequently on their thermally induced decomposition. The formation of solid solutions of Fe−Cu oxalates with various Fe/Cu ratios was studied by energy dispersive X-ray analysis, X-ray powder diffraction, transmission 57Fe Mössbauer spectroscopy, and scanning electron microscopy. The results suggest that the bimetal Fe−Cu oxalate precipitated in a structure similar to β-FeC2O4 ⋅ 2H2O. The maximum relative amount of Cu obtained within the bimetal oxalate was approximately 40 %. However, the single bimetal phase composition was obtained only for a limited range of Fe/Cu ratios. The Fe-rich samples contained also β-FeC2O4 ⋅ 2H2O, while the Cu-rich samples were predominantly composed of CuC2O4 ⋅ nH2O and contained much lower amounts of Fe than expected. The thermal decomposition of the prepared oxalate with the nominal Fe/Cu ratio of 65/35 was studied by in-situ X-ray powder diffraction in combination with ex-situ Mössbauer spectroscopy. The mixing of both metals at the molecular level allowed the preparation of copper ferrite particles at a relatively low temperature of 470 °C.

  • Název v anglickém jazyce

    Co-Precipitation of Fe—Cu Bimetal Oxalates in an Aqueous Solution and Their Thermally Induced Decomposition

  • Popis výsledku anglicky

    This work focuses on the preparation of bimetal Fe−Cu oxalates by a co-precipitation reaction in an aqueous solution and subsequently on their thermally induced decomposition. The formation of solid solutions of Fe−Cu oxalates with various Fe/Cu ratios was studied by energy dispersive X-ray analysis, X-ray powder diffraction, transmission 57Fe Mössbauer spectroscopy, and scanning electron microscopy. The results suggest that the bimetal Fe−Cu oxalate precipitated in a structure similar to β-FeC2O4 ⋅ 2H2O. The maximum relative amount of Cu obtained within the bimetal oxalate was approximately 40 %. However, the single bimetal phase composition was obtained only for a limited range of Fe/Cu ratios. The Fe-rich samples contained also β-FeC2O4 ⋅ 2H2O, while the Cu-rich samples were predominantly composed of CuC2O4 ⋅ nH2O and contained much lower amounts of Fe than expected. The thermal decomposition of the prepared oxalate with the nominal Fe/Cu ratio of 65/35 was studied by in-situ X-ray powder diffraction in combination with ex-situ Mössbauer spectroscopy. The mixing of both metals at the molecular level allowed the preparation of copper ferrite particles at a relatively low temperature of 470 °C.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    21001 - Nano-materials (production and properties)

Návaznosti výsledku

  • Projekt

  • Návaznosti

    S - Specificky vyzkum na vysokych skolach

Ostatní

  • Rok uplatnění

    2021

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY

  • ISSN

    1434-1948

  • e-ISSN

  • Svazek periodika

    2021

  • Číslo periodika v rámci svazku

    37

  • Stát vydavatele periodika

    DE - Spolková republika Německo

  • Počet stran výsledku

    10

  • Strana od-do

    3886-3895

  • Kód UT WoS článku

    000693316600001

  • EID výsledku v databázi Scopus

    2-s2.0-85114159322