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超声辅助提取/单颗粒电感耦合等离子体质谱法测定防晒化妆品中的纳米二氧化钛
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作者单位
梁维新,刘宁,郭鹏然,严冬 1.广东省测试分析研究所广东省化学危害应急检测技术重点实验室2.安捷伦科技(中国)有限公司安捷伦-中广测联合技术中心 
基金项目:广东省科学院科技创新发展专项(2016GDASPTGDASCX-0203);国家自然科学基金项目(21777150,21707128);广东省科技计划项目(2017A070702017)
中文摘要:建立了超声辅助提取/单颗粒电感耦合等离子体质谱(SP-ICP-MS)测定防晒化妆品中纳米TiO2的方法。考察了停留时间、纳米粒子数量及浓度等分析条件,确定了防晒化妆品中纳米TiO2的最佳萃取条件以及测定方法,对比了不同萃取溶剂对防晒霜中纳米TiO2的提取效果。结果表明,在采用01% Tritonx-100(Tx-100)以及5%乙醇作为萃取剂超声辅助提取,测定停留时间为3 ms,待测样品中纳米颗粒的数量浓度低于4×107 个/mL条件下,该法可准确测定防晒化妆品中的纳米TiO2,对防晒化妆品中纳米TiO2的数量浓度检出限(LODconc)为1×104 个/mL,纳米颗粒粒度检出限(LODsize)为35 nm。方法简单快捷、灵敏度高、准确性良好,可同时对防晒化妆品中TiO2进行浓度测定及粒度分布表征。
中文关键词:单颗粒电感耦合等离子体质谱法  超声辅助提取  纳米TiO2  防晒化妆品
 
Determination of Nano TiO2 in Sunscreen by Single Particle Inductively Coupled Plasma-Mass Spectrometry with Ultrasound assisted Extraction
Abstract:A novel method combining ultrasound assisted extraction with single particle inductively coupled plasma-mass spectrometry(SP-ICP-MS)was developed for the analysis of nano TiO2 in sunscreen.To obtain the optimal extraction and analysis conditions,the experimental factors such as extraction solvents,dwell time and number concentration of nano TiO2 were investigated.Result showed that the optimum dwell time was 3 ms and the upper concentration limit for nano TiO2 was 4×107 particles/mL.The nano TiO2 in sunscreen could be extracted effectively by ultrasound assisted extraction with 01% Tritonx-100 and 5% ethanol as extracting agents.The method could be used for the detection on nano TiO2 in sunscreen with a detection limit for number concentration(LODconc)of 1×104 particles/mL and a detection limit for particle size(LODsize)of 35 nm.With the advantages of simplicity,rapidness,good sensitivity and accuracy,the method could be applied in the simultaneous determination and characterization on concentration and particle size distribution of nano TiO2 in sunscreen.
Key Words:single particle inductively coupled plasma-mass spectrometry(SP-ICP-MS)  ultrasound assisted extraction  nano TiO2  sunscreen
引用本文:梁维新,刘宁,郭鹏然,严冬.超声辅助提取/单颗粒电感耦合等离子体质谱法测定防晒化妆品中的纳米二氧化钛[J].分析测试学报,2018,37(10):1238-1243.
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