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Synthesis of Calcium Ferrite Nanoparticles (CaFe_2O_4-NPs) Using Auto-Combustion Method for Targeted Drug Delivery

机译:使用自燃方法对靶向药物递送的自燃方法合成铁氧体纳米粒子(CaFe_2O_4-NPS)

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In this paper, we report the synthesis process development of calcium ferrite nanoparticles (CaFe_2O_4 NPs) using auto-combustion method. The process started by mixing the calcium nitrate Ca(NO_2)_3 and ferric nitrate Fe(NO_3)_3 dissolved in 150mL of distilled water with an addition of citric acid as a chelating agent. The mixture was synthesized through sol-gel combustion method and then calcined at 550°C to obtain powders. The crystalline structure and surface morphology of CaFe_2O_4 NPs were observed and characterized by using XRD and FESEM measurement, while the magnetic property of the synthesize particles was analyzed by using VSM. Analysis results through XRD showed that an orthorhombic structure of calcium ferrite NPs was observed. The analysis using the transmission electron microscopy (FESEM) and VSM measurement showed that the particle size of CaFe_2O_4 nanoparticles ranging from 5 To 20 nm was obtained. While the magnetic saturation (M_s) was 31.1emu/g for auto-combustion method with good magnetic properties. The magnetic property of the synthesized particles was also compared with that synthesized using a standard sol-gel method. This work will give important information about an alternative technique to synthesize the Calcium Ferrite magnetic nanoparticles used for targeted drug delivery application.
机译:在本文中,我们使用自燃方法报道了铁素体纳米粒子(Cafe_2O_4 NPS)的合成过程开发。通过将溶解在150ml蒸馏水中的硝酸钙Ca(NO_2)_3和铁硝酸铁Fe(NO_3)_3的方法开始,加入柠檬酸作为螯合剂。通过溶胶 - 凝胶燃烧方法合成混合物,然后在550℃下煅烧以获得粉末。通过使用XRD和FESEM测量,观察和表征CaFe_2O_4 NP的结晶结构和表面形态,同时通过使用VSM分析合成颗粒的磁性。通过XRD分析结果表明,观察到铁素体NP的正晶间结构。使用透射电子显微镜(FESEM)和VSM测量的分析表明,获得从5至20nm的CaFe_2O_4纳米颗粒的粒度。虽然磁饱和度(M_S)为31.1EMU / g,用于具有良好磁性的自燃方法。将合成颗粒的磁性与使用标准溶胶 - 凝胶法合成的合成的磁性相比。这项工作将提供关于合成用于靶向药物递送应用的钙铁氧体磁性纳米粒子的替代技术的重要信息。

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