Synthesis and formation mechanism of amorphous silica particles via sol–gel process with tetraethylorthosilicate

材料科学 硅酸 成核 化学工程 傅里叶变换红外光谱 粒径 无定形固体 纳米颗粒 粒子(生态学) 光谱学 纳米技术 有机化学 化学 工程类 地质学 物理 海洋学 量子力学
作者
Xianfa Jiang,Xiaoning Tang,Lihong Tang,Bin Zhang,Huaming Mao
出处
期刊:Ceramics International [Elsevier BV]
卷期号:45 (6): 7673-7680 被引量:65
标识
DOI:10.1016/j.ceramint.2019.01.067
摘要

Silica microspheres with narrow particle size distribution and average diameter of 80–200 nm were prepared by hydrolysis and condensation of tetraethylorthosilicate (TEOS) in ethanol solution. Effects of TEOS, ammonia, water concentration, and temperature on particle size and morphology were investigated by laser particle size analysis and field emission scanning electron microscopy (FESEM), in conjunction with energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) spectroscopy. Monomer addition model was employed to analyze the stability of intermediate, as well as the direction in which the reaction of silica particles proceeds. The analysis was carried out by Materials Studio. Results demonstrated that particle size of Nano-silica increases with increasing concentrations of H2O, NH3·H2O, and TEOS in ethanol, whereas the size decreases with increasing temperature. In addition, when proper amount of H2O was added into NH3·H2O at suitable temperature, silicic acid can act as a nucleus for amorphous Nano-silica particles, forming microspheres with round and smooth surfaces. By contrast, when TEOS was used, resultant nanoparticles have poor surfaces. During nucleation process of Nano-silica, silicic acid can also acts as nucleating agent providing a platform for the growth of nanoparticles with symmetric structure. Findings further indicated that the reaction proceeds by first silicic acid participates in the reaction, and the dimer and trimer molecules then react with the surface of silicic acid molecules; the same products could be produced by different reactions.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Sun发布了新的文献求助10
1秒前
叶伟帮发布了新的文献求助10
1秒前
小毛驴完成签到,获得积分10
1秒前
愿713发布了新的文献求助10
1秒前
量子星尘发布了新的文献求助10
1秒前
花露水发布了新的文献求助10
1秒前
希望天下0贩的0应助佳佳采纳,获得10
2秒前
2秒前
叶伟帮发布了新的文献求助10
2秒前
亭子完成签到 ,获得积分10
2秒前
三点半完成签到 ,获得积分10
2秒前
2秒前
王翼完成签到,获得积分10
2秒前
香蕉觅云应助优雅的纸鹤采纳,获得10
3秒前
4秒前
4秒前
4秒前
共享精神应助teborlee采纳,获得10
5秒前
科研通AI5应助呜呜采纳,获得10
5秒前
彩色的德地完成签到,获得积分10
6秒前
研友_VZG7GZ应助tyZhang采纳,获得10
7秒前
鲑鱼归鱼完成签到,获得积分20
7秒前
7秒前
从容不乐发布了新的文献求助10
8秒前
Owen应助珍珠球采纳,获得10
8秒前
paz_1010完成签到,获得积分10
8秒前
8秒前
完美世界完成签到,获得积分10
9秒前
康康米其林完成签到,获得积分10
9秒前
9秒前
Ava应助贪玩菲音采纳,获得10
9秒前
9秒前
MZCCaiajie发布了新的文献求助10
9秒前
爱lx发布了新的文献求助10
10秒前
琦琦发布了新的文献求助10
10秒前
wh完成签到,获得积分10
10秒前
XU应助搞科研的小李同学采纳,获得10
10秒前
SciGPT应助bacteria采纳,获得10
11秒前
美丽万声完成签到 ,获得积分10
11秒前
所所应助潇飞天下采纳,获得10
11秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Acute Mountain Sickness 2000
Handbook of Milkfat Fractionation Technology and Application, by Kerry E. Kaylegian and Robert C. Lindsay, AOCS Press, 1995 1000
A novel angiographic index for predicting the efficacy of drug-coated balloons in small vessels 500
Textbook of Neonatal Resuscitation ® 500
The Affinity Designer Manual - Version 2: A Step-by-Step Beginner's Guide 500
Affinity Designer Essentials: A Complete Guide to Vector Art: Your Ultimate Handbook for High-Quality Vector Graphics 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 5071945
求助须知:如何正确求助?哪些是违规求助? 4292467
关于积分的说明 13374776
捐赠科研通 4113406
什么是DOI,文献DOI怎么找? 2252418
邀请新用户注册赠送积分活动 1257312
关于科研通互助平台的介绍 1190103