纺织品%全氟化合物%痕量分析%液相色谱串联质谱法%同位素内标法
紡織品%全氟化閤物%痕量分析%液相色譜串聯質譜法%同位素內標法
방직품%전불화합물%흔량분석%액상색보천련질보법%동위소내표법
textile%perfluorinated compounds (PFCs)%trace analysis%high performance liquid chromatography-mass spectrometry (HPLC/MS/MS)%isotope-labeled internal standard method
采用超声法提取纺织品中的全氟化合物.以C18为分析柱,甲醇-5 mmol/L乙酸铵为梯度洗脱淋洗液,13 min内即可分离全氟已酸(PFHxA),全氟辛酸 (PFOA),全氟壬酸(PFNA),全氟癸酸 (PFDA),全氟十一酸(PFuDA),全氟十二酸(PFDoA),全氟丁烷磺酸(PFBS),全氟已烷磺酸(PFHxS),全氟辛烷磺酸(PFOS),全氟癸烷磺酸(PFDS) 10 种分析物.以313.1/268.9, 12.9/368.9, 462.9/418.9, 512.7/468.9, 562.7/518.9, 612.8/568.9, 298.8/99, 399.2/99, 498.8/99, 599/99分别对PFHxA,PFOA,PFNA,PFDA,PFuDA,PFDoA,PFBS,PFHxS,PFOS,PFDS 进行监控和定量分析.利用同位素内标法进行定量,线性范围和添加回收率分别为0.5~10μg/m2、84.6%~111.8%,检出限为0.5 μg/m2,低于欧盟指定针对纺织品1 μg/m2 的限定.结果表明,本方法准确、快速,并成功用于20种纺织品实样的检测.
採用超聲法提取紡織品中的全氟化閤物.以C18為分析柱,甲醇-5 mmol/L乙痠銨為梯度洗脫淋洗液,13 min內即可分離全氟已痠(PFHxA),全氟辛痠 (PFOA),全氟壬痠(PFNA),全氟癸痠 (PFDA),全氟十一痠(PFuDA),全氟十二痠(PFDoA),全氟丁烷磺痠(PFBS),全氟已烷磺痠(PFHxS),全氟辛烷磺痠(PFOS),全氟癸烷磺痠(PFDS) 10 種分析物.以313.1/268.9, 12.9/368.9, 462.9/418.9, 512.7/468.9, 562.7/518.9, 612.8/568.9, 298.8/99, 399.2/99, 498.8/99, 599/99分彆對PFHxA,PFOA,PFNA,PFDA,PFuDA,PFDoA,PFBS,PFHxS,PFOS,PFDS 進行鑑控和定量分析.利用同位素內標法進行定量,線性範圍和添加迴收率分彆為0.5~10μg/m2、84.6%~111.8%,檢齣限為0.5 μg/m2,低于歐盟指定針對紡織品1 μg/m2 的限定.結果錶明,本方法準確、快速,併成功用于20種紡織品實樣的檢測.
채용초성법제취방직품중적전불화합물.이C18위분석주,갑순-5 mmol/L을산안위제도세탈림세액,13 min내즉가분리전불이산(PFHxA),전불신산 (PFOA),전불임산(PFNA),전불계산 (PFDA),전불십일산(PFuDA),전불십이산(PFDoA),전불정완광산(PFBS),전불이완광산(PFHxS),전불신완광산(PFOS),전불계완광산(PFDS) 10 충분석물.이313.1/268.9, 12.9/368.9, 462.9/418.9, 512.7/468.9, 562.7/518.9, 612.8/568.9, 298.8/99, 399.2/99, 498.8/99, 599/99분별대PFHxA,PFOA,PFNA,PFDA,PFuDA,PFDoA,PFBS,PFHxS,PFOS,PFDS 진행감공화정량분석.이용동위소내표법진행정량,선성범위화첨가회수솔분별위0.5~10μg/m2、84.6%~111.8%,검출한위0.5 μg/m2,저우구맹지정침대방직품1 μg/m2 적한정.결과표명,본방법준학、쾌속,병성공용우20충방직품실양적검측.
Ultrasonic method was used to extract PFCs from textiles,and the pretreatment process is convenient.The ten kinds of target compounds,i.e.PFHxA,PFOA,PFNA,PFDA,PFuDA,PFDoA,PFBS,PFHxS,PFOS,and PFDS were separated on C18 reversed phase column in 13 min with step methanol-5 mmoL/L ammonium acetate as the mobile phase.Monitor and qualitative analysis of PFHxA,PFOA,PFNA,PFDA,PFuDA,PFDoA,PFBS,PFHxS,PFOS,PFDS were undertaken at 313.1/268.9,412.9/368.9,462.9/418.9,512.7/468.9,562.7/518.9,612.8/568.9,298.8/99,399.2/99,498.8/99,599/99 respectively.Isotope-labeled internal standard method was used to carry out such tests as the limit of detection,linear range,and recovery range.The results showed they were 0.5μg/m2,0.5-10μg/m2, and 84.6%-111.8%, respectively .It should be pointed out that the limit of detection is 0.μ/m2 by this method which is lower than 1μg/m2 regulated for textiles by EU. This method was accurate and swift,which has been successfully applied to analyze 20 real textile samples.