中华纸业
中華紙業
중화지업
CHINA PULP & PAPER INDUSTRY
2014年
4期
15-20
,共6页
多环芳烃%超声萃取%纸质食品接触材料%气相色谱/质谱-选择离子监测法
多環芳烴%超聲萃取%紙質食品接觸材料%氣相色譜/質譜-選擇離子鑑測法
다배방경%초성췌취%지질식품접촉재료%기상색보/질보-선택리자감측법
polycyclic aromatic hydrocarbons%ultrasonic extraction%paper packaging materials intended to come into contact with foodstuffs%gas chromatography/mass spectrometry-selected ion monitor technique
建立了一个气相色谱/质谱-选择离子监测方法,对纸质食品接触材料中18种禁用多环芳烃进行了同时测定,该方法以正己烷/丙酮(1∶1)为提取溶剂,40℃下超声提取纸质食品接触材料中的多环芳烃,提取产物经硅胶固相萃取柱净化后进行气相色谱/质谱-选择离子监测法测定,外标法定量。在S/N=3的条件下,各目标化合物的检出限为0.1~1.0μg/kg。方法的加标平均回收率为55.98~95.62%,相对标准偏差为2.87~6.98%,线性相关系数均大于0.997。该方法快速简便,定性准确,检出限低,可完全满足多环芳烃检测的技术要求,可用于食品接触材料中18种禁用多环芳烃的同时测定。采用该方法对市售食品接触材料进行测试,结果在米黄色再生包装纸袋中检出高含量的菲。
建立瞭一箇氣相色譜/質譜-選擇離子鑑測方法,對紙質食品接觸材料中18種禁用多環芳烴進行瞭同時測定,該方法以正己烷/丙酮(1∶1)為提取溶劑,40℃下超聲提取紙質食品接觸材料中的多環芳烴,提取產物經硅膠固相萃取柱淨化後進行氣相色譜/質譜-選擇離子鑑測法測定,外標法定量。在S/N=3的條件下,各目標化閤物的檢齣限為0.1~1.0μg/kg。方法的加標平均迴收率為55.98~95.62%,相對標準偏差為2.87~6.98%,線性相關繫數均大于0.997。該方法快速簡便,定性準確,檢齣限低,可完全滿足多環芳烴檢測的技術要求,可用于食品接觸材料中18種禁用多環芳烴的同時測定。採用該方法對市售食品接觸材料進行測試,結果在米黃色再生包裝紙袋中檢齣高含量的菲。
건립료일개기상색보/질보-선택리자감측방법,대지질식품접촉재료중18충금용다배방경진행료동시측정,해방법이정기완/병동(1∶1)위제취용제,40℃하초성제취지질식품접촉재료중적다배방경,제취산물경규효고상췌취주정화후진행기상색보/질보-선택리자감측법측정,외표법정량。재S/N=3적조건하,각목표화합물적검출한위0.1~1.0μg/kg。방법적가표평균회수솔위55.98~95.62%,상대표준편차위2.87~6.98%,선성상관계수균대우0.997。해방법쾌속간편,정성준학,검출한저,가완전만족다배방경검측적기술요구,가용우식품접촉재료중18충금용다배방경적동시측정。채용해방법대시수식품접촉재료진행측시,결과재미황색재생포장지대중검출고함량적비。
An effective gas chromatography/mass spectrometry-selected ion monitoring method was established for the simultaneous determination of the contents of 18 kinds of banned polycyclic aromatic hydrocarbons (PAHs) in paper packaging materials intended to come into contact with foodstuffs. PAHs in paper packaging materials intended to come into contact with foodstuffs were ifrst ultrasonically extracted at 40℃, using hexane/acetone (1:1) as the extraction solvent, then the extract was purified by silica solid phase extraction column, followed by the analysis of gas chromatography/mass spectrometry-selected ion monitor technique. The concentration of each analytes was calibrated by external standard method. The detection limits changed from 0.1μg/kg to 1.0μg/kg at the condition of signal to noise (S/N) of 3. The spiked average recoveries varied from 55.98% to 95.62% while the relative standard deviation (RSD) changed from 2.87% to 6.98%. At the same time, the coefficients were all larger than 0.997. The proposed method was simple, rapid, accurate and sensitive, and could satisfy completely the demand of the analysis of PAHs in paper packaging materials intended to come into contact with foodstuffs. This method was applied to the simultaneous determination of PAHs in commercially available paper packaging materials intended to come into contact with foodstuffs and phennanthrene of high content was detected in a warm beige regenerated packing bag.