色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2009年
6期
760-763
,共4页
刘志杏%郭平%王远兴%占春瑞%左海根
劉誌杏%郭平%王遠興%佔春瑞%左海根
류지행%곽평%왕원흥%점춘서%좌해근
气相色谱%苯丁锡%残留%柑橘
氣相色譜%苯丁錫%殘留%柑橘
기상색보%분정석%잔류%감귤
gas chromatography (GC)%fenbutatin oxide (FBT)%residue%orange
建立了气相色谱-火焰光度检测器测定柑橘类水果中苯丁锡残留量的检测方法.样品在酸性条件下经丙酮及正己烷萃取并浓缩,用正己烷溶解残渣,经乙基溴化镁衍生后,采用硅胶固相萃取柱净化,正己烷-二氯甲烷(体积比为4∶1)混合液洗脱,用毛细管气相色谱-火焰光度检测器(锡滤光片:610 nm)测定,外标法定量.结果表明:该方法的线性范围为0.2~2.0 mg/L,相关系数r≥0.999 5;当阴性脐橙样品中加标水平为0.1~0.4 mg/kg 时,苯丁锡的回收率为79.6% ~109.6%,相对标准偏差为3.60% ~9.05%,方法的检出限为0.1 mg/kg.该方法重复性好,灵敏度高,完全满足国内外柑橘类水果中苯丁锡残留分析的要求.
建立瞭氣相色譜-火燄光度檢測器測定柑橘類水果中苯丁錫殘留量的檢測方法.樣品在痠性條件下經丙酮及正己烷萃取併濃縮,用正己烷溶解殘渣,經乙基溴化鎂衍生後,採用硅膠固相萃取柱淨化,正己烷-二氯甲烷(體積比為4∶1)混閤液洗脫,用毛細管氣相色譜-火燄光度檢測器(錫濾光片:610 nm)測定,外標法定量.結果錶明:該方法的線性範圍為0.2~2.0 mg/L,相關繫數r≥0.999 5;噹陰性臍橙樣品中加標水平為0.1~0.4 mg/kg 時,苯丁錫的迴收率為79.6% ~109.6%,相對標準偏差為3.60% ~9.05%,方法的檢齣限為0.1 mg/kg.該方法重複性好,靈敏度高,完全滿足國內外柑橘類水果中苯丁錫殘留分析的要求.
건립료기상색보-화염광도검측기측정감귤류수과중분정석잔류량적검측방법.양품재산성조건하경병동급정기완췌취병농축,용정기완용해잔사,경을기추화미연생후,채용규효고상췌취주정화,정기완-이록갑완(체적비위4∶1)혼합액세탈,용모세관기상색보-화염광도검측기(석려광편:610 nm)측정,외표법정량.결과표명:해방법적선성범위위0.2~2.0 mg/L,상관계수r≥0.999 5;당음성제등양품중가표수평위0.1~0.4 mg/kg 시,분정석적회수솔위79.6% ~109.6%,상대표준편차위3.60% ~9.05%,방법적검출한위0.1 mg/kg.해방법중복성호,령민도고,완전만족국내외감귤류수과중분정석잔류분석적요구.
An analytical method for the determination of fenbutatin oxide ( FBT) residue in oranges by capillary gas chromatography-flame photometric detection ( GC-FPD) was devel-oped. The FBT was extracted with acetone-acetic acid (99= 1, v/v) and hexane, filtered and evaporated by nitrogen evaporator in a water bath at 35 ℃. The residue was dissolved in hex-ane. The FBT in the solvent was derivatized with ethyl magnesium bromide for 15 min, 1 mol/L hydrochloride was added, the supernatant was collected and the solvent was evaporated to get dry supernatants, then the supernatant was dissolved in hexane and cleaned up with a silica solid phase extraction column, eluted with 5 mL hexane-dichloromethane (4:1, v/v), deter-mined by GC. The standard curve was linear in the range of 0. 2 - 2. 0 mg/L. The correlation coefficients (r) were more than 0.999 5, the average recoveries were 79. 6%-109.6% with the relative standard deviations (RSDs) of 3. 60%-9. 04% at the spiked levels of 0. 1-0. 4 mg/kg, and the detection limit of fenbutatin oxide was 0.1 mg/kg. This method is suitable for the anal-ysis of fenbutatin oxide residue in orange products.