首页 | 本学科首页   官方微博 | 高级检索  
     

电泳沉积用羟基磷灰石稳定悬浮液的制备
引用本文:朱庆霞,韩丹,李双.电泳沉积用羟基磷灰石稳定悬浮液的制备[J].硅酸盐通报,2017,36(12):4122-4128.
作者姓名:朱庆霞  韩丹  李双
作者单位:景德镇陶瓷大学材料科学与工程学院,景德镇,333001
基金项目:国家自然科学基金(51462014)%江西省教育厅科研项目(GJJ160868)
摘    要:研究了羟基磷灰石粉体粒径、粉体预烧温度、陈化时间、分散溶剂、悬浮液固含量对羟基磷灰石悬浮液稳定性的影响,通过测定Zeta电位,吸光度等参数表征悬浮液稳定性,对悬浮液电泳沉积的涂层进行SEM表面形貌及粘结-拉伸结合强度的表征.结果表明:悬浮液颗粒越小,Zeta电位越高;对羟基磷灰石粉体预烧800℃,Zeta电位明显提高,且有利于涂层与基体的结合;悬浮液陈化48 h后,颗粒荷电性最佳,可得致密均匀的涂层;以乙二醇为分散溶剂可制备稳定的悬浮液,但乙醇溶剂更有利于涂层的电泳沉积;悬浮液固含量控制为20g/L时,涂层质量较好.

关 键 词:电泳沉积  羟基磷灰石  悬浮液稳定性  Zeta电位  

Preparation of Stabilized Hydroxyapatite Suspension for Electrophoretic Deposition
ZHU Qing-xia,HAN Dan,LI Shuang.Preparation of Stabilized Hydroxyapatite Suspension for Electrophoretic Deposition[J].Bulletin of the Chinese Ceramic Society,2017,36(12):4122-4128.
Authors:ZHU Qing-xia  HAN Dan  LI Shuang
Abstract:The effects of hydroxyapatite particle size , pre-treatment temperature , aging time , dispersion solvent and solid content on the stability of hydroxyapatite suspension were studied .The stability of suspension was characterized by zeta potential and absorbance parameters .And the surface morphologies of coatings were characterized by SEM .The bonding strength between the coating and substrate was tested by shear strength testing experiment .The results show that the smaller the suspension particles , the higher the Zeta potential .Pre-heat treatment at 800 ℃of apatite powders can improve the Zeta potential of suspensions and the bonding strength between the coating and the substrate .The suspension system charges best after aging for 48 h, dense and uniform coating can be obtained .Although stable suspension can be obtained by taking the ethylene glycol as dispersing solvent , ethanol solvent is more conducive to the electrophoretic deposition of the coating .The suspension solid content at 20 g/L can get better quality of coating .
Keywords:electrophoretic deposition  hydroxyapatite  suspension stability  Zeta potential  
本文献已被 CNKI 等数据库收录!
点击此处可从《硅酸盐通报》浏览原始摘要信息
点击此处可从《硅酸盐通报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号