Rohit R. Powar, Ashok B. Gadkari, Pravina B. Piste, Dnyandevo N. Zambare
{"title":"Synthesis and characterization study of dual phase mixed zinc cobalt ferrite nanoparticles prepared via chemical co-precipitation method","authors":"Rohit R. Powar, Ashok B. Gadkari, Pravina B. Piste, Dnyandevo N. Zambare","doi":"10.5185/amp2018/6997","DOIUrl":null,"url":null,"abstract":"Nanoparticles of Zinc substituted Cobalt ferrite powders having general formula ZnxCo1-xFe2O4 (x = 0, 0.25, 0.5, 0.75, 1.0) have been produced by using analytical grade nitrates and hexadecyltrimethylammonium bromide (CTAB) as structure directing reagent via Chemical co-precipitation method. The structure and morphology of prepared polycrystalline ferrite nanoparticles were investigated by X-ray diffraction (XRD), Fourier Transform Infrared Radiation (FTIR) and Scanning electron microscopy (SEM) respectively. Thermogravimetric differential analysis (TG/DTA) technique gives information about ferrite phase formation occurs beyond 450 oC. The XRD analysis confirms the establishment of the cubic spinel structure with the presence of minor secondary phase of α-Fe2O3 (hematite) at a calcination temperature of 650 oC. The polycrystalline mixed zinc cobalt ferrite nanoparticles showed a dual phase and crystallite size lies in the range 6-11 nm. FE-SEM microstructure shows the nearly spherical polycrystalline nanoparticles with a particle size in between 0.11-0.20 μm. The FT-IR spectra display two significant strong absorption bands nearby in the range of 400 cm and 600 cm on the tetrahedral and octahedral sites respectively. Copyright © 2018 VBRI Press.","PeriodicalId":7297,"journal":{"name":"Advanced Materials Proceedings","volume":"6 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials Proceedings","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5185/amp2018/6997","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
化学共沉淀法制备双相混合锌钴铁氧体纳米颗粒的合成及表征研究
采用化学共沉淀法,以分析级硝酸盐和十六烷基三甲基溴化铵(CTAB)为结构导向剂,制备了通式为ZnxCo1-xFe2O4 (x = 0、0.25、0.5、0.75、1.0)的锌取代钴铁氧体纳米颗粒。采用x射线衍射(XRD)、傅里叶变换红外辐射(FTIR)和扫描电镜(SEM)对制备的多晶铁氧体纳米颗粒的结构和形貌进行了研究。热重差析(TG/DTA)技术提供了450℃以上铁氧体相形成的信息。XRD分析证实,在650℃的煅烧温度下,形成了立方尖晶石结构,α-Fe2O3(赤铁矿)次级相少量存在。多晶混合锌钴铁氧体纳米颗粒呈双相结构,晶粒尺寸在6 ~ 11 nm之间。FE-SEM显微结构显示为近球形多晶纳米颗粒,粒径在0.11 ~ 0.20 μm之间。FT-IR光谱分别在四面体和八面体的400 cm和600 cm附近有两个明显的强吸收带。版权所有©2018 VBRI出版社。
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