磁性材料及器件
磁性材料及器件
자성재료급기건
JOURNAL OF MAGNETIC MATERIALS AND DEVICES
2014年
6期
20-22,80
,共4页
冯杰%邓黎明%蔡钢%刘曦
馮傑%鄧黎明%蔡鋼%劉晞
풍걸%산려명%채강%류희
Fe3O4纳米粒子%超顺磁性%超声辅助共沉淀%饱和磁化强度%分散性
Fe3O4納米粒子%超順磁性%超聲輔助共沉澱%飽和磁化彊度%分散性
Fe3O4납미입자%초순자성%초성보조공침정%포화자화강도%분산성
nano-Fe3O4%superparamagnetism%ultrasound-assisted coprecipitation%saturation magnetization%dispersity
采用超声波辅助部分还原共沉淀法制备超顺磁性Fe3O4纳米粒子。采用红外光谱仪(FT-IR)、X射线衍射(XRD)、振动样品磁强计(VSM)和粒径测试等手段对磁性纳米粒子进行表征,研究了不同表面改性剂(油酸、十二烷基苯磺酸钠、葡聚糖)对制备的磁性粒子的晶粒尺寸、磁性能及颗粒分散性的影响。结果表明,采用表面活性剂包覆改性后Fe3O4纳米粒子的XRD峰明显宽化,晶粒直径由未改性的18.5nm减小至6.0~9.0nm,饱和磁化强度因晶粒尺寸的减小而降低,且改性后颗粒在溶液中的分散性提高。
採用超聲波輔助部分還原共沉澱法製備超順磁性Fe3O4納米粒子。採用紅外光譜儀(FT-IR)、X射線衍射(XRD)、振動樣品磁彊計(VSM)和粒徑測試等手段對磁性納米粒子進行錶徵,研究瞭不同錶麵改性劑(油痠、十二烷基苯磺痠鈉、葡聚糖)對製備的磁性粒子的晶粒呎吋、磁性能及顆粒分散性的影響。結果錶明,採用錶麵活性劑包覆改性後Fe3O4納米粒子的XRD峰明顯寬化,晶粒直徑由未改性的18.5nm減小至6.0~9.0nm,飽和磁化彊度因晶粒呎吋的減小而降低,且改性後顆粒在溶液中的分散性提高。
채용초성파보조부분환원공침정법제비초순자성Fe3O4납미입자。채용홍외광보의(FT-IR)、X사선연사(XRD)、진동양품자강계(VSM)화립경측시등수단대자성납미입자진행표정,연구료불동표면개성제(유산、십이완기분광산납、포취당)대제비적자성입자적정립척촌、자성능급과립분산성적영향。결과표명,채용표면활성제포복개성후Fe3O4납미입자적XRD봉명현관화,정립직경유미개성적18.5nm감소지6.0~9.0nm,포화자화강도인정립척촌적감소이강저,차개성후과립재용액중적분산성제고。
Superparamagnetic Fe3O4 nanoparticles were synthesized via a modified coprecipitation method, and were characterized with FTIR, XRD, VSM and DLS, respectively. The influences of kinds of surfactants (oleic acid, sodium dodecyl benzene sulfonate and dextran) on the grain size, magnetic properties and dispersity were investigated. The results show that, the peaks of XRD patterns of the modified Fe3O4 nanoparticles have an obviously broadening. Comparing with unmodified sample, the mean grain size of modified Fe3O4 nanoparticles decrease from 18.5 nm to 6.0-9.0 nm, and the saturation magnetization decreases, which attributes to the decrease of crystalline size and a non-magnetic covering layer coated on the surface of Fe3O4 nanoparticle. And surfactants greatly improve the dispersion of Fe3O4 nanoparticles.