分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2014年
9期
1354-1358
,共5页
于彦彬%张嵘%李莉%杨君%谭丕功%刘宗兴
于彥彬%張嶸%李莉%楊君%譚丕功%劉宗興
우언빈%장영%리리%양군%담비공%류종흥
液相色谱-串联质谱法%苯氧羧酸类除草剂%固相萃取%土壤
液相色譜-串聯質譜法%苯氧羧痠類除草劑%固相萃取%土壤
액상색보-천련질보법%분양최산류제초제%고상췌취%토양
Solid phase extraction%Liquid chromatography tandem mass spectrometry%Phenoxy acid herbicides%Soil
建立了基质校正液相色谱-串联质谱( HPLC-MS/MS)同时测定土壤中9种苯氧羧酸类除草剂残留量的分析方法。样品用含1.5%甲酸的乙腈溶液超声提取两次,提取液经氨基柱净化后,使用C18色谱柱,以含甲酸的水溶液和甲醇为流动相,在梯度条件下进行分离。在多级反应离子监测( MRM)负离子模式下进行质谱数据采集,采用两对离子进行定性和定量分析。9种苯氧羧酸类除草剂在2~250μg/L浓度范围内呈线性关系,相关系数为0.9929~0.9972;检出限在1.7~3.8μg/kg之间。土壤中9种苯氧羧酸类除草剂的3个浓度水平加标的平均回收率为85.3%~110.0%,相对标准偏差在3.2%~12.0%之间。
建立瞭基質校正液相色譜-串聯質譜( HPLC-MS/MS)同時測定土壤中9種苯氧羧痠類除草劑殘留量的分析方法。樣品用含1.5%甲痠的乙腈溶液超聲提取兩次,提取液經氨基柱淨化後,使用C18色譜柱,以含甲痠的水溶液和甲醇為流動相,在梯度條件下進行分離。在多級反應離子鑑測( MRM)負離子模式下進行質譜數據採集,採用兩對離子進行定性和定量分析。9種苯氧羧痠類除草劑在2~250μg/L濃度範圍內呈線性關繫,相關繫數為0.9929~0.9972;檢齣限在1.7~3.8μg/kg之間。土壤中9種苯氧羧痠類除草劑的3箇濃度水平加標的平均迴收率為85.3%~110.0%,相對標準偏差在3.2%~12.0%之間。
건립료기질교정액상색보-천련질보( HPLC-MS/MS)동시측정토양중9충분양최산류제초제잔류량적분석방법。양품용함1.5%갑산적을정용액초성제취량차,제취액경안기주정화후,사용C18색보주,이함갑산적수용액화갑순위류동상,재제도조건하진행분리。재다급반응리자감측( MRM)부리자모식하진행질보수거채집,채용량대리자진행정성화정량분석。9충분양최산류제초제재2~250μg/L농도범위내정선성관계,상관계수위0.9929~0.9972;검출한재1.7~3.8μg/kg지간。토양중9충분양최산류제초제적3개농도수평가표적평균회수솔위85.3%~110.0%,상대표준편차재3.2%~12.0%지간。
A method for the determination of 9 phenoxy acid herbicides in soil by solid phase extraction and LC/MS/MS with matrix correction was developed. The sample was treated by ultrasonic extraction twice with 1. 5% formic acid in acetonitrile. The extract was cleaned up with NH2 solid phase extraction column. A C18 column with formic acid in pure water/methanol mixture as the mobile phase was used under gradient elution. Mass spectral acquisition was done in negative ion mode by multiple reactions monitoring ( MRM ) . Two transitions per compound were used to provide qualitative and quantitative analysis. There were good linear relationships in the range of 2-250 μg/L for 9 phenoxy acid herbicides. The correlation coefficients were in the range of 0 . 9927-0 . 9972 . The method detection limits were in the range of 1 . 66-3 . 82 μg/kg . The average recoveries at three spiked levels ( 10 , 40 , 200 μg/kg ) ranged from 85 . 3% to 110 . 0% with the relative standard deviations (RSD) of 3. 2%-12%.