摘要
采用易于工业化的液相沉淀法,在十二烷基硫酸钠(SDS)和烷基多苷(APG)复配溶液的协同作用下,合成了收率98%左右的改性纳米氢氧化镁。通过沉降体积法,N2吸附,X射线衍射,红外光谱,透射电镜等手段对样品进行了表征分析,结果表明所得样品分散性好,结晶度高。相对于未改性样品,改性样品(复配表面活性剂质量比1∶1,添加量0.2%)的沉降百分含量提高了31.2%,比表面积增大了10.62 m2/g,堆密度降低了0.150 g/mL。通过机理探讨,发现SDS和APG可能以单分子层或双分子层形式吸附到样品表面,它们主要依靠长碳链的空间位阻效应影响晶核微粒的团聚,从而得到分散性优良的片状样品。
The surface modified nano-sized magnesium hydroxide was synthesized by mixed surfactant wet precipitation method(SDS and APG as modification) and yield is about 98%.The attained samples were characterized by sediment volume,N2 adsorption,X-ray diffraction,fourier transform infrared spectroscopy,transmission electron microscope.The experimental results show that the samples synthesized have good dispersion and crystal.Compared with the unmodified sample,when mass ratio of SDS and APG is 1 ∶1and 0.2% mix surfactant is added,sediment volume percent increases by 31.2%,surface area increases by 10.62 m2/g,and Bulk density declines by 0.150 g/mL.It is discovered that SDS and APG maybe adsorb the surface of sample via odd molecular or double molecular in order to arrest conglomeration of crystal and good dispersion sample is obtained.
出处
《盐业与化工》
CAS
2010年第3期12-16,共5页
Jounral of Salt and Chemical Industry
基金
山西省重点实验室开放基金(2008012013-11)
关键词
纳米氢氧化镁
复配的表面活性剂
改性
机理
nanometer magnesium hydroxide
mixed surfactants
modification
mechanism