Abstract

Via a mild thermal precipitation and aging process, polycrystalline hydrated nickel oxalate nanofibers were synthesized using nickel chloride and ammonium oxalate as raw materials, with pH 8.0 and temperature 60 °C. Atomic absorption spectrometer (AAS), organic elemental analyzer (OEA), fourier transform infrared spectroscopy (FT-IR), thermogravimetry-derivative thermogravimetry (TG-DTG), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to characterize the products properties. The results demonstrated that the product was hydrated nickel oxalate. The sizes of hydrated nickel oxalate nanofibers were 100–150 nm in diameter, and 0.5–5.0 μm in length. A rational mechanism based on coordination self-assembly was discussed for the selective formation of the polycrystalline hydrated nickel oxalate nanofibers.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.