中国环境监测
中國環境鑑測
중국배경감측
ENVIRONMENTAL MONITORING IN CHINA
2014年
1期
119-124
,共6页
李昆%赵高峰%周怀东%张盼伟%余丽琴%文武%刘晓茹%常佩丽
李昆%趙高峰%週懷東%張盼偉%餘麗琴%文武%劉曉茹%常珮麗
리곤%조고봉%주부동%장반위%여려금%문무%류효여%상패려
生物介质%溴代阻燃剂%凝胶渗透色谱%硅胶柱%气相色谱-负化学离子源质谱
生物介質%溴代阻燃劑%凝膠滲透色譜%硅膠柱%氣相色譜-負化學離子源質譜
생물개질%추대조연제%응효삼투색보%규효주%기상색보-부화학리자원질보
biological medium%brominated flame retardants%gel permeation chromatography%silica-gel column%gas chromatography-mass spectrometry-negative chemical ionization
建立了生物介质内22种多溴联苯( PBBs)和27种多溴联苯醚( PBDEs)的净化和分析方法。通过分析不同时间段凝胶渗透色谱( GPC)洗脱液中49种化合物含量,得出不同化合物凝胶色谱洗脱曲线。样品经过凝胶渗透色谱-混合硅胶柱净化后,再使用GC-( NCI)/MS对样品进行检测。实验结果表明,PBBs和PBDEs检出限分别为0?02~0?88 pg/g和0?01~74?00 pg/g。对实验过程进行验证发现,样品不同浓度加标回收率为80%~120%,相对标准偏差小于20%。该方法具有良好的净化效果、准确度和精密度,拥有良好的线性范围及检出限,满足生物介质中溴代阻燃剂的检测分析实际要求。
建立瞭生物介質內22種多溴聯苯( PBBs)和27種多溴聯苯醚( PBDEs)的淨化和分析方法。通過分析不同時間段凝膠滲透色譜( GPC)洗脫液中49種化閤物含量,得齣不同化閤物凝膠色譜洗脫麯線。樣品經過凝膠滲透色譜-混閤硅膠柱淨化後,再使用GC-( NCI)/MS對樣品進行檢測。實驗結果錶明,PBBs和PBDEs檢齣限分彆為0?02~0?88 pg/g和0?01~74?00 pg/g。對實驗過程進行驗證髮現,樣品不同濃度加標迴收率為80%~120%,相對標準偏差小于20%。該方法具有良好的淨化效果、準確度和精密度,擁有良好的線性範圍及檢齣限,滿足生物介質中溴代阻燃劑的檢測分析實際要求。
건립료생물개질내22충다추련분( PBBs)화27충다추련분미( PBDEs)적정화화분석방법。통과분석불동시간단응효삼투색보( GPC)세탈액중49충화합물함량,득출불동화합물응효색보세탈곡선。양품경과응효삼투색보-혼합규효주정화후,재사용GC-( NCI)/MS대양품진행검측。실험결과표명,PBBs화PBDEs검출한분별위0?02~0?88 pg/g화0?01~74?00 pg/g。대실험과정진행험증발현,양품불동농도가표회수솔위80%~120%,상대표준편차소우20%。해방법구유량호적정화효과、준학도화정밀도,옹유량호적선성범위급검출한,만족생물개질중추대조연제적검측분석실제요구。
A method has been developed for the clean-up and determination of 22 polybrominated biphenyls ( PBBs ) and 27 polybrominated diphenyl ethers ( PBDEs) in biological medium. The eluting profiles of 49 compounds were established according to the results of GC quantitation with the eluted liquids in different collecting time. The samples were purified using gel permeation chromatography ( GPC) to eliminate most of the lipids and waxes. Multi-layer silica gel was further used to remove the pigments. The quantitative analysis was performed with GC-( NCI )/MS for polybrominated biphenyls and polybrominated biphenyl ethers. The limits of detection of 22 PBBs were in range of 0?02-0?88 ng/L, while 27 PBDEs were in range of 0?01-74?00 ng/L. The average fortified and coefficients of variation of the method were determined. The results showed that recoveries were between 80%-120% and the relative standard deviations were less than 20%. This method is precise, sensitive and highly efficient in extraction. After routine applications, the results indicated that this method is suitable for the determination of BFRs contents in the biological medium.