Flower-like microparticles and novel superparamagnetic properties of new binary Co<inf>1/2</inf>Fe<inf>1/2</inf>(H<inf>2</inf>PO<inf>4</inf>)<inf>2</inf>·2H<inf>2</inf>O obtained by a rapid solid state route at ambient temperature

A new binary Co1/2Fe1/2(H2PO4)2·2H2O was synthesized by a simple, rapid and cost-effective method using CoCO3-Fe(c)-H3PO4system at ambient temperature. Thermal treatment of the obtained Co1/2Fe1/2(H2PO4)2·2H2O at 600 °C yielded as a binary cobalt iron cyclotetraphosphate CoFeP4O12. The FTIR and XRD...

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Bibliographic Details
Main Authors: Banjong Boonchom, Montree Thongkam, Samart Kongtaweelert, Naratip Vittayakorn
Other Authors: King Mongkut's Institute of Technology Ladkrabang
Format: Article
Published: 2018
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/27540
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Institution: Mahidol University
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Summary:A new binary Co1/2Fe1/2(H2PO4)2·2H2O was synthesized by a simple, rapid and cost-effective method using CoCO3-Fe(c)-H3PO4system at ambient temperature. Thermal treatment of the obtained Co1/2Fe1/2(H2PO4)2·2H2O at 600 °C yielded as a binary cobalt iron cyclotetraphosphate CoFeP4O12. The FTIR and XRD results of the synthesized Co1/2Fe1/2(H2PO4)2·2H2O and its final decomposed product CoFeP4O12indicate the monoclinic phases with space group P21/n and C2/c, respectively. The particle morphologies of both binary metal compounds appear the flower-like microparticle shapes. Room temperature magnetization results show novel superparamagnetic behaviors of the Co1/2Fe1/2(H2PO4)2·2H2O and its final decomposed product CoFeP4O12, having no hysteresis loops in the range of ±10,000 Oe with the specific magnetization values of 0.045 and 12.502 emu/g at 10 kOe, respectively. The dominant physical properties of the obtained binary metal compounds (Co1/2Fe1/2(H2PO4)2·2H2O and CoFeP4O12) are compared with the single compounds (M(H2PO4)2·2H2O and M2P4O12; where M = Co, Fe), indicating the presence of Co ions in substitution position of Fe ions. © 2009 Elsevier Ltd. All rights reserved.