M. Mirbagheri , O. Mirzaee , M. Tajally , H. Shokrollahi
{"title":"球磨加热法制备Mn–Zn颗粒的合成、结构、高温行为及磁性能","authors":"M. Mirbagheri , O. Mirzaee , M. Tajally , H. Shokrollahi","doi":"10.1016/j.physo.2023.100139","DOIUrl":null,"url":null,"abstract":"<div><p>This paper has focused upon the synthesis, structure, hyperthermia and magnetic properties of the Mn–Zn particles prepared by a new combined ball milling and heating process. Normally, it is required that the partial pressure in the final sintering be controlled by the Mn–Zn ferrite preparation, yet in the current method the ferrite has been obtained with a nearly high purity. The nanocrystalline Mn<sub>1-x</sub>Zn<sub>x</sub>Fe<sub>2</sub>O<sub>4</sub> (x = 0.25, 0.5 and 0.75) powders were characterized using the X-ray diffractometer (XRD), field emission scanning electron microscope (FESEM), transmission electron microscope (TEM), Raman spectrometer (RS), Fourier-transform infrared spectrometer (FTIR), vibrating sample magnetometer (VSM) and specific absorption rate (SAR). The FTIR and Raman data confirmed the result of the XRD data and the presence of spinel structure. The zinc content affected the band lengths, cation distributions and particle sizes. The structural results revealed that as the Zn concentration increases, the particle size decreases and the other cations tend to go to the octahedral sites. The results demonstrated that the highest level of SAR corresponds to the efficient and non-toxic Mn<sub>0.75</sub>Zn<sub>0.25</sub>Fe<sub>2</sub>O<sub>4</sub> due to the suitable particle size and noticeable saturation magnetization.</p></div>","PeriodicalId":36067,"journal":{"name":"Physics Open","volume":"14 ","pages":"Article 100139"},"PeriodicalIF":0.0000,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Synthesis, structure, hyperthermia behavior and magnetic properties of Mn–Zn particles prepared by a new method of ball-milling and heating\",\"authors\":\"M. Mirbagheri , O. Mirzaee , M. Tajally , H. Shokrollahi\",\"doi\":\"10.1016/j.physo.2023.100139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This paper has focused upon the synthesis, structure, hyperthermia and magnetic properties of the Mn–Zn particles prepared by a new combined ball milling and heating process. Normally, it is required that the partial pressure in the final sintering be controlled by the Mn–Zn ferrite preparation, yet in the current method the ferrite has been obtained with a nearly high purity. The nanocrystalline Mn<sub>1-x</sub>Zn<sub>x</sub>Fe<sub>2</sub>O<sub>4</sub> (x = 0.25, 0.5 and 0.75) powders were characterized using the X-ray diffractometer (XRD), field emission scanning electron microscope (FESEM), transmission electron microscope (TEM), Raman spectrometer (RS), Fourier-transform infrared spectrometer (FTIR), vibrating sample magnetometer (VSM) and specific absorption rate (SAR). The FTIR and Raman data confirmed the result of the XRD data and the presence of spinel structure. The zinc content affected the band lengths, cation distributions and particle sizes. The structural results revealed that as the Zn concentration increases, the particle size decreases and the other cations tend to go to the octahedral sites. The results demonstrated that the highest level of SAR corresponds to the efficient and non-toxic Mn<sub>0.75</sub>Zn<sub>0.25</sub>Fe<sub>2</sub>O<sub>4</sub> due to the suitable particle size and noticeable saturation magnetization.</p></div>\",\"PeriodicalId\":36067,\"journal\":{\"name\":\"Physics Open\",\"volume\":\"14 \",\"pages\":\"Article 100139\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physics Open\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666032623000042\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Physics and Astronomy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physics Open","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666032623000042","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Physics and Astronomy","Score":null,"Total":0}
Synthesis, structure, hyperthermia behavior and magnetic properties of Mn–Zn particles prepared by a new method of ball-milling and heating
This paper has focused upon the synthesis, structure, hyperthermia and magnetic properties of the Mn–Zn particles prepared by a new combined ball milling and heating process. Normally, it is required that the partial pressure in the final sintering be controlled by the Mn–Zn ferrite preparation, yet in the current method the ferrite has been obtained with a nearly high purity. The nanocrystalline Mn1-xZnxFe2O4 (x = 0.25, 0.5 and 0.75) powders were characterized using the X-ray diffractometer (XRD), field emission scanning electron microscope (FESEM), transmission electron microscope (TEM), Raman spectrometer (RS), Fourier-transform infrared spectrometer (FTIR), vibrating sample magnetometer (VSM) and specific absorption rate (SAR). The FTIR and Raman data confirmed the result of the XRD data and the presence of spinel structure. The zinc content affected the band lengths, cation distributions and particle sizes. The structural results revealed that as the Zn concentration increases, the particle size decreases and the other cations tend to go to the octahedral sites. The results demonstrated that the highest level of SAR corresponds to the efficient and non-toxic Mn0.75Zn0.25Fe2O4 due to the suitable particle size and noticeable saturation magnetization.