表面技术
錶麵技術
표면기술
Surface Technology
2015年
9期
72-77
,共6页
复合纳米微粒%核-壳结构%Fe(NO3)3处理%磁化强度%抗腐蚀层
複閤納米微粒%覈-殼結構%Fe(NO3)3處理%磁化彊度%抗腐蝕層
복합납미미립%핵-각결구%Fe(NO3)3처리%자화강도%항부식층
composite nanoparticles%core-shell structure%Fe( NO3 ) 3 treatment%magnetization strength%anti-corrosion layer
目的:研究经Fe( NO3)3处理后γ-Fe2 O3/Ni2 O3复合纳米微粒稳定分散在磁性液体中的机理。方法使用共沉淀法制备FeOOH/Ni(OH)2前躯体,经FeCl2溶液处理后得到以γ-Fe2O3为核心,Ni2O3在外层,FeCl3·6H2 O在最外层的核-壳结构γ-Fe2 O3/Ni2 O3复合纳米微粒。用硝酸铁溶液对其进一步处理,使微粒表面性质稳定以适合配制离子型磁性液体。使用振动样品磁强计、透射电子显微镜、X射线衍射仪、X射线光电子能谱仪对硝酸铁处理后复合纳米微粒的磁性、形态、晶体结构、化学组成及结构进行分析。结果经硝酸铁处理后,微粒的磁性减弱,粒径略微变大,约为11 nm,但位于微粒核心的主要成分γ-Fe2O3保持不变,且在微粒表面包裹了一层Fe(NO3)3·9H2O抗腐蚀层。结论经Fe(NO3)3处理后微粒表面包裹的抗腐蚀层及配制磁性液体时微粒表面吸附同种H+或OH-形成的静电斥力,使微粒在磁性液体中稳定分散。
目的:研究經Fe( NO3)3處理後γ-Fe2 O3/Ni2 O3複閤納米微粒穩定分散在磁性液體中的機理。方法使用共沉澱法製備FeOOH/Ni(OH)2前軀體,經FeCl2溶液處理後得到以γ-Fe2O3為覈心,Ni2O3在外層,FeCl3·6H2 O在最外層的覈-殼結構γ-Fe2 O3/Ni2 O3複閤納米微粒。用硝痠鐵溶液對其進一步處理,使微粒錶麵性質穩定以適閤配製離子型磁性液體。使用振動樣品磁彊計、透射電子顯微鏡、X射線衍射儀、X射線光電子能譜儀對硝痠鐵處理後複閤納米微粒的磁性、形態、晶體結構、化學組成及結構進行分析。結果經硝痠鐵處理後,微粒的磁性減弱,粒徑略微變大,約為11 nm,但位于微粒覈心的主要成分γ-Fe2O3保持不變,且在微粒錶麵包裹瞭一層Fe(NO3)3·9H2O抗腐蝕層。結論經Fe(NO3)3處理後微粒錶麵包裹的抗腐蝕層及配製磁性液體時微粒錶麵吸附同種H+或OH-形成的靜電斥力,使微粒在磁性液體中穩定分散。
목적:연구경Fe( NO3)3처리후γ-Fe2 O3/Ni2 O3복합납미미립은정분산재자성액체중적궤리。방법사용공침정법제비FeOOH/Ni(OH)2전구체,경FeCl2용액처리후득도이γ-Fe2O3위핵심,Ni2O3재외층,FeCl3·6H2 O재최외층적핵-각결구γ-Fe2 O3/Ni2 O3복합납미미립。용초산철용액대기진일보처리,사미립표면성질은정이괄합배제리자형자성액체。사용진동양품자강계、투사전자현미경、X사선연사의、X사선광전자능보의대초산철처리후복합납미미립적자성、형태、정체결구、화학조성급결구진행분석。결과경초산철처리후,미립적자성감약,립경략미변대,약위11 nm,단위우미립핵심적주요성분γ-Fe2O3보지불변,차재미립표면포과료일층Fe(NO3)3·9H2O항부식층。결론경Fe(NO3)3처리후미립표면포과적항부식층급배제자성액체시미립표면흡부동충H+혹OH-형성적정전척력,사미립재자성액체중은정분산。
Objective To investigate the mechanism ofγ-Fe2 O3/Ni2 O3 composite nanoparticle stably dispersed in the ferrofluids after Fe( NO3 ) 3 treatment. Methods The FeOOH/Ni( OH) 2 precursor was prepared by coprecipitation, and was then treated with the FeCl2 solution to obtain composite nanoparticles containingγ-Fe2 O3 core, Ni2 O3 external shell and FeCl3 ·6H2 O outermost lay-er. The nanoparticles were then treated with Fe( NO3 ) 3 to obtain modified particles with stable surface properties for the preparation of ionic ferrofluids. The magneticity, morphology, crystal structure, chemical composition and structure of the composite nanoparti-cles after Fe( NO3 ) 3 treatment were analyzed by VSM, TEM, XRD, EDX and XPS. Results The particles after treatment were slightly larger ( about 11 nm) , but the major componentγ-Fe2 O3 located in the core of particles remained unchanged. And the sur-face of the particles was covered with a Fe(NO3)3·9H2O corrosion-resistant layer. Conclusion The corrosion-resistant layer cov-ering the particles after Fe( NO3 ) 3 treatment and the electrostatic repulsion formed by the same species H+ or OH- adsorbed onto the surface of the particles during the preparation of magnetic liquid made the particles stably dispersed in the ferrofluids.