摘要
0 1mol/LHCl-4 0mg/mLTritonX 100-0 05mol/LBaCl2溶液体系的同步散射很弱,加入SO2-4浓度在4后,形成的(BaSO4)n微粒在470nm处产生一较强同步散射峰,SO2-2 0～80μg/mL浓度范围内与I470呈线性关系,据此建立了一个简便灵敏的测定水泥样品中硫酸根的同步散射光谱分析新方法。其相对标准偏差(RSD)在1 3%～2 7%之间,回收率在98 4%～101%之间。研究结果表明,由于静电引力SO2-4与Ba2+之间可形成BaSO4分子,而BaSO4分子间存在较强疏水作用力和分子间作用力可聚集形成(BaSO4)n微粒和固液界面,(BaSO4)n微粒和固液界面的形成是导致体系同步散射增强的根本原因。
There is very weak synchronous scattering for the system of 0.1 mol/L HCl - 4.0 mol/L Triton X-100 - 0.05 mol/L BaCl2. When SO42- is added, Ba2+ reacts with SO42- to form (BaSO4)n particles. The particle has a strong synchronous scattering peak at 470 nm. The synchronous scattering intensity at 470 nm is linear to SO42- concentration in the range of 2.0 - 80 μg/mL. And a novel synchronous scattering spectral method has been described for the determination of SO42- in cement samples. The method is simple and sensitive. Its RSD is in the range of 1.3% -2.7%, and the recovery is in the range of 98.4% - 101%.The results show that SO42- and Ba2+ combine to BaSO4 molecule by means of electrostatic force. The BaSO4 molecules form (BaSO4)n particles and solid-liquid interface owing to existence of strong hydrophobic interaction and intermolecular forces. Both of the particle and interface bring about the enhancement of synchronous scattering intensity.
出处
《冶金分析》
EI
CAS
CSCD
北大核心
2005年第2期13-16,共4页
Metallurgical Analysis
基金
国家自然科学基金(20175018
20036501)
广西自然科学基金资助项目
