分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2010年
1期
67-71
,共5页
林福华%邱宁宁%黄晓佳%袁东星
林福華%邱寧寧%黃曉佳%袁東星
림복화%구저저%황효가%원동성
搅拌棒固相萃取%整体材料%高效液相色谱%双酚A%辛基酚%壬基酚
攪拌棒固相萃取%整體材料%高效液相色譜%雙酚A%辛基酚%壬基酚
교반봉고상췌취%정체재료%고효액상색보%쌍분A%신기분%임기분
Stir bar sorptive extraction%Monolithic material%High performance liquid chromatography/diode array detector%Bisphenol A%Octyphenol%Nonylphenol
建立了简单、快速、灵敏测定水环境中的双酚A(BPA)、辛基酚(OP)、壬基酚(NP)的方法.以聚(N-乙烯基咪唑-二乙烯基苯)整体材料为涂层的搅拌棒同相萃取技术富集目标物,然后与高效液相色谱-二极管阵列检测器联用测定水样品中烷基酚类污染物.考察了萃取时间、解析时间、样品基质的pH值、离子强度等实验条件对萃取效率的影响.在最佳条件下,3种目标化合物的线性范围是1.0~200μg/L,检出限LOD(S/N=3)在0.13~0.66μg/L之间,定量限LOQ(S/N=10)在0.44~2.μg/L之间.在对海水和污水处理厂的实际水样测定中,3种目标化合物的不同加标水平的回收率为37.8%~101.1%.本方法具有简便、快速、高效、灵敏等优点.
建立瞭簡單、快速、靈敏測定水環境中的雙酚A(BPA)、辛基酚(OP)、壬基酚(NP)的方法.以聚(N-乙烯基咪唑-二乙烯基苯)整體材料為塗層的攪拌棒同相萃取技術富集目標物,然後與高效液相色譜-二極管陣列檢測器聯用測定水樣品中烷基酚類汙染物.攷察瞭萃取時間、解析時間、樣品基質的pH值、離子彊度等實驗條件對萃取效率的影響.在最佳條件下,3種目標化閤物的線性範圍是1.0~200μg/L,檢齣限LOD(S/N=3)在0.13~0.66μg/L之間,定量限LOQ(S/N=10)在0.44~2.μg/L之間.在對海水和汙水處理廠的實際水樣測定中,3種目標化閤物的不同加標水平的迴收率為37.8%~101.1%.本方法具有簡便、快速、高效、靈敏等優點.
건립료간단、쾌속、령민측정수배경중적쌍분A(BPA)、신기분(OP)、임기분(NP)적방법.이취(N-을희기미서-이을희기분)정체재료위도층적교반봉동상췌취기술부집목표물,연후여고효액상색보-이겁관진렬검측기련용측정수양품중완기분류오염물.고찰료췌취시간、해석시간、양품기질적pH치、리자강도등실험조건대췌취효솔적영향.재최가조건하,3충목표화합물적선성범위시1.0~200μg/L,검출한LOD(S/N=3)재0.13~0.66μg/L지간,정량한LOQ(S/N=10)재0.44~2.μg/L지간.재대해수화오수처리엄적실제수양측정중,3충목표화합물적불동가표수평적회수솔위37.8%~101.1%.본방법구유간편、쾌속、고효、령민등우점.
A method for the determination of bisphenol A, octyphenol, nonylphenol in water samples was developed using stir bar sorptive extraction (SBSE) based on poly (vinylimidazole-divinylbenzene) monolithic material (SBSEM) combined with high performance liquid chromatography with diode array detection.To achieve the optimum extraction performance, several main extraction parameters, including extraction and desorption time, pH value and contents of inorganic salt in the sample matrix, were investigated.Under the optimized experimental conditions, the method showed good linearity and repeatability, low detection limits (S/N = 3) and quantification limits (S/N = 10) of the proposed method for the target compounds were achieved within the range of 0.13-0.66 and 0.44-2.19 μg/L, respectively.The extraction performance of SBSEM to the target compounds was also compared with commercial SBSE which used polydimethylsiloxane as coating.The proposed method was successfully applied to the determination of the target compounds in water samples.The recoveries of spiked target compounds in real samples ranged from 37.8%-101.1%.The results indicated that the developed method possessed advantages such as sensitivity, simplicity, low cost and high feasibility.