化学研究与应用
化學研究與應用
화학연구여응용
CHEMICAL RESEARCH AND APPLICATION
2014年
7期
988-992
,共5页
朱建君%翟秋阁%李晓玲%朱锦锦%于心爱
硃建君%翟鞦閣%李曉玲%硃錦錦%于心愛
주건군%적추각%리효령%주금금%우심애
纳米SiO2%硅烷偶联剂%表面改性%界面相互作用
納米SiO2%硅烷偶聯劑%錶麵改性%界麵相互作用
납미SiO2%규완우련제%표면개성%계면상호작용
nano-SiO2%Silane coupling agent%surface modification%interface interaction
采用KH550为硅烷偶联剂对纳米SiO2进行改性,对改性前后的纳米SiO2采用XRD、TEM、FTIR、NMR等表征手段研究样品的微观结构、表面羟基含量、有机/无机界面相互作用等问题。实验结果表明,纳米SiO2经过KH550的改性,亲水性减弱、亲油性增强,表面质子运动活性也随之增加,并且KH550与SiO2有相互作用存在。29 Si核的NMR谱表明,由于KH550与纳米SiO2表面的偶极相互作用,分子运动变慢,使得纳米SiO2改性后的29 Si弛豫时间比改性前明显增加。
採用KH550為硅烷偶聯劑對納米SiO2進行改性,對改性前後的納米SiO2採用XRD、TEM、FTIR、NMR等錶徵手段研究樣品的微觀結構、錶麵羥基含量、有機/無機界麵相互作用等問題。實驗結果錶明,納米SiO2經過KH550的改性,親水性減弱、親油性增彊,錶麵質子運動活性也隨之增加,併且KH550與SiO2有相互作用存在。29 Si覈的NMR譜錶明,由于KH550與納米SiO2錶麵的偶極相互作用,分子運動變慢,使得納米SiO2改性後的29 Si弛豫時間比改性前明顯增加。
채용KH550위규완우련제대납미SiO2진행개성,대개성전후적납미SiO2채용XRD、TEM、FTIR、NMR등표정수단연구양품적미관결구、표면간기함량、유궤/무궤계면상호작용등문제。실험결과표명,납미SiO2경과KH550적개성,친수성감약、친유성증강,표면질자운동활성야수지증가,병차KH550여SiO2유상호작용존재。29 Si핵적NMR보표명,유우KH550여납미SiO2표면적우겁상호작용,분자운동변만,사득납미SiO2개성후적29 Si이예시간비개성전명현증가。
The surface of nano-SiO2 particles was modified with silane coupling agent(3-aminopropyl triethoxysilane,KH550). X-ray diffraction(XRD),Transmission electron microscope(TEM),Fourier transform infrared spectroscop(FTIR)and Nuclear Magnetic Resonance( NMR) were adopted to characterize and analyze microstructure,surface hydroxyl content,organic-inorganic interface in-teraction of the unmodified and modified nano-SiO2 particles. The results indicated that after surface modification, hydrophilic of nano-SiO2 weakened,hydrophobic of nano-SiO2 increased, and interactions between KH550 and nano-SiO2 existed. Moreover,29 Si NMR indicated that because of the existence of dipole interactions between KH550 and nano-SiO2 ,molecular motion slowed down, and 29 Si relaxation time of KH550 modified nano-SiO2 were longer than that of nano-SiO2 .