摘要
以氯化镁为镁源,氨水为沉淀剂,分别采用正向、反向和双向三种滴定过程制备Mg(OH)2,通过监测溶液动态pH值变化,并引入晶体生长驱动力指标S(镁与氢氧根离子积与容度积的比值取对数)来定量表示溶液滴定过程中动态过饱和度变化,SEM和XRD表征Mg(OH)2的结构和形貌。结果表明,正向滴定过程合成的Mg(OH)2晶粒大小混杂(100~600nm),反向滴定合成的晶粒偏小(200nm左右),双向滴定合成的晶粒粒径分布集中(400nm左右)。引入的S值较能准确地描述Mg(OH)2成核和晶体生长的规律,不同的滴定过程有不同的S值变化规律。联系S值的变化和晶体粒径的分布,认为S〉0时晶体成核占主导,S〈0时晶体生长占主导。通过动态控制溶液S值的动态变化,可以目的性地控制Mg(OH)2晶体的结构和形貌。
Magnesium hydroxide was prepared by ordinal-titration method, reverse-titration method and double-titration method, pH of the solution was controlled during the titration process, and S value, which point to the growth of Mg (OH)2 crystal force, was used to show the dynamic variation of supersaturation in quantity. The samples were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD). The results show that the Mg(OH) 2 by ordinal-titration was made up of the larger particle (600 nm)and smaller(-100nm) , while the particle size was decreased to 200 nm by reversetitration, and centered at 400 nm by double-titration. S value was obviously different in the three titration processes, and it could be used to describe the growth of Mg(OH) 2 crystal more exactly. Compared the S value with the particle size distribution of Mg (OH) 2, it can be inferred that when S 〉 0, nucleation is dominant ;S 〈 0, growth is dominant. Therefore, the morphologies and sizes of Mg ( OH ) 2 could be controlled by tuning the S value.
出处
《人工晶体学报》
EI
CAS
CSCD
北大核心
2008年第5期1249-1254,共6页
Journal of Synthetic Crystals
基金
浙江省科技厅重点资助项目(No.2006C21079)
关键词
氢氧化镁
滴定过程
晶体形貌
粒径
Mg( OH ) 2
titration process
crystal morphology
oarticle size