|
|||||
|
|
| 气相色谱-质谱法测定水体中5种典型有机紫外防晒剂 | |
| 引用本文： | 丁怡然,黄云,赵婷婷,蔡倩,罗玉,黄斌,张榆霞,潘学军.气相色谱-质谱法测定水体中5种典型有机紫外防晒剂[J].色谱,2014,32(6):629-634. |
| 作者姓名： | 丁怡然 黄云 赵婷婷 蔡倩 罗玉 黄斌 张榆霞 潘学军 |
| 作者单位： | 1. 昆明理工大学环境科学与工程学院, 云南 昆明 650500; 2. 云南省环境监测中心站, 云南 昆明 650034 |
| 基金项目： | 国家自然科学基金项目(21267012);高等学校博士学科点专项科研基金项目(20125314110003);云南省应用基础研究计划项目(2012FB124) |
| 摘 要： | 建立了水体中5种典型有机紫外防晒剂甲氧基肉桂酸乙基己酯(ethylhexyl methoxycinnamate,EHMC)、二苯酮-3(benzophenone-3,BP-3)、4-甲基苄亚基樟脑(4-methylbenzylidene camphor,4-MBC)、奥克立林(octocrylene,OC)和胡莫柳酯(homosalate,HMS)的气相色谱-质谱检测方法。对HMS、BP-3衍生化条件进行了系统的优化。以100μL双(三甲基硅烷基)三氟乙酰胺(N,O-bis(trimethylsilyl)trifluoroacetamide,BSTFA)为衍生化试剂,在100℃下反应100 min。水样固相萃取选用Oasis HLB萃取柱(0.5 g),洗脱溶剂为乙酸乙酯-二氯甲烷(1∶1,v/v),水样pH3~5。该方法对5种化合物的检出限范围为0.5~1.2 ng/L,定量限范围为1.4~4.0 ng/L。最佳实验条件下,加标水样回收率为87.85%~102.34%,相对标准偏差(n=3)均小于5%。该方法成功地应用于昆明市第一污水厂进出口水样中目标物质的分析。 |
| 关 键 词： | 衍生化 固相萃取 气相色谱-质谱法 有机紫外防晒剂 水样 |
| 收稿时间： | 2014-01-20 |
Determination of five representative ultraviolet filters in water by gas chromatography-mass spectrometry |
|
| DING Yiran;HUANG Yun;ZHAO Tingting;CAI Qian;LUO Yu;HUANG Bin;ZHANG Yuxia;PAN Xuejun.Determination of five representative ultraviolet filters in water by gas chromatography-mass spectrometry[J].Chinese Journal of Chromatography,2014,32(6):629-634. | |
| Authors: | DING Yiran;HUANG Yun;ZHAO Tingting;CAI Qian;LUO Yu;HUANG Bin;ZHANG Yuxia;PAN Xuejun |
| Affiliation: | 1. Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming 650500, China; 2. Yunnan Environmental Monitoring Center, Kunming 650034, China |
| Abstract: | A method for the determination of five representative organic UV filters: ethylhexyl methoxycinnamate (EHMC), benzophenone-3 (BP-3), 4-methylbenzylidene camphor (4-MBC), octocrylene (OC), homosalate (HMS) in water was investigated. The method was based on derivatization, solid phase extraction (SPE), followed by determination with gas chromatography-mass spectrometry (GC-MS). The variables involved in the derivatization of BP-3 and HMS were optimized, and SPE conditions were studied. For derivatization, 100 μL N,O-bis(trimethylsilyl) trifluoroacetamide (BSTFA) was used as derivatization reagent and reacted with BP-3 and HMS at 100 ℃ for 100 min. For SPE, the pH value of water sample was adjusted to 3-5. The Oasis HLB cartridges were employed and the solution of ethyl acetate and dichloromethane (1:1, v/v) was used as the eluting solvent, and good recoveries of the target compounds were obtained. The limits of detection (LODs) and the limits of quantification (LOQs) for the five target compounds in water samples were 0.5-1.2 ng/L and 1.4-4.0 ng/L, respectively. The recoveries of spiked water samples were 87.85%-102.34% with good repeatability and reproducibility (RSD<5%, n=3) for all the target compounds. Finally, the validated method was applied to analysis the representative UV filters in water samples collected from a wastewater treatment plant in Kunming city of Yunnan province. |
| Keywords: | derivatization solid phase extraction (SPE) gas chromatography-mass spectrometry (GC-MS) organic ultraviolet filters water sample |
| 本文献已被 CNKI 等数据库收录！ | |
| 点击此处可从《色谱》浏览原始摘要信息 | |
| 点击此处可从《色谱》下载全文 | |
