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GC-MS法测定塑胶跑道面层中的6种有害物质
引用本文:周良春,张晓飞,马俊辉,李双琦.GC-MS法测定塑胶跑道面层中的6种有害物质[J].塑料,2020,49(1):134-138.
作者姓名:周良春  张晓飞  马俊辉  李双琦
作者单位:成都产品质量检验研究院有限责任公司,国家包装产品质量监督检验中心,成都市产品质量监督检验院,四川,成都610100;成都产品质量检验研究院有限责任公司,国家包装产品质量监督检验中心,成都市产品质量监督检验院,四川,成都610100;成都产品质量检验研究院有限责任公司,国家包装产品质量监督检验中心,成都市产品质量监督检验院,四川,成都610100;成都产品质量检验研究院有限责任公司,国家包装产品质量监督检验中心,成都市产品质量监督检验院,四川,成都610100
摘    要:建立了检测塑胶跑道面层中6种有害物质(环己基异氰酸酯(CHI)、2,4-甲苯二异氰酸酯(2,4-TDI)、2,6-甲苯二异氰酸酯(2,6-TDI)、六亚甲基二异氰酸酯(HDI)、萘-1,5-二异氰酸酯(NDI)和4,4'-二苯基甲烷二异氰酸酯(4,4'-MDI))含量的GC-MS检测方法,分别讨论了定量方式和萃取时间对6种有害物质回收率的影响。将样品剪碎至10~20目(0.85~2.00 mm)的颗粒,用10 mL乙酸乙酯萃取,室温下超声20 min,提取液用DB-17MS石英毛细管色谱柱(30 m×0.25 mm×0.25μm)分离,采用GC-MS法并选择离子检测,内标法定量。结果表明,在0.5~100.0 mg/L(4,4'-MDI在1.0~100.0 mg/L)浓度范围内,线性良好,相关系数均大于0.998,方法检出限范围为2.0~10.0 mg/kg,定量限范围为6.0~20.0 mg/kg;加标平均回收率在80.1%~100.8%之间,相对标准偏差(n=6)小于5.2%。该方法快速、准确,适用于塑胶跑道面层中有害物质的测定。

关 键 词:气相色谱质谱法  塑胶跑道  二异氰酸酯  超声提取  有害物质

Determination of 6 Harmful Substances in Surface Layer of Plastic Runway by Gas Chromatography-Mass Spectrometry
ZHOU Liangchun,ZHANG Xiaofei,MA Junhui,LI Shuangqi.Determination of 6 Harmful Substances in Surface Layer of Plastic Runway by Gas Chromatography-Mass Spectrometry[J].Plastics,2020,49(1):134-138.
Authors:ZHOU Liangchun  ZHANG Xiaofei  MA Junhui  LI Shuangqi
Affiliation:(Chengdu Institute of Product Quality Inspection and Research Co.,Ltd.,National Center for Packaging Material Quality Supervision and Inspection,Chengdu Institute of Product Quality Supervision and Inspection,Chengdu,Sichuan 610100,China)
Abstract:A method was developed for the determination of 6 harmful substances(cyclohexyl isocyanate(CHI),2,4-toluene diisocyanate(2,4-TDI),2,6-toluene diisocyanate(2,6-TDI),hexamethylene diisocyanate(HDI),naphthalene-1,5-diisocyanate(NDI)and 4,4'-diphenylmethane diisocyanate(4,4'-MDI))in surface layer of plastic runway by gas chromatography-mass spectrometer(GC-MS).The effects of recovery of 6 harmful substances by different quantitative methods and extraction time were discussed,respectively.The samples were cut to 20 to 10 meshe sieve(0.85~2.00 mm),extracted with 10 mL ethyl acetate for 20 min at room temperature.The samples were separated into DB-17MS quartz capillary column(30 m×0.25 mm×0.25μm).The samples were separated by GC-MS and quantified by internal standard method.The results showed that the correlation coefficientsr were more than 0.998,in the range of 0.5~100.0 mg/L(4,4'-MDI,0.5~100.0 mg/L).The limits of detection(LODs)were 2.0~10.0 mg/kg,the limits of quantitation(LOQs)were 6.0~20.0 mg/kg.The average recovery rate ranged from 80.1%to 100.8%,and the relative standard deviations(n=6)were less than 5.2%.This method could be suitable for the determination of harmful substances in surface layer of plastic runway rapidly and accurately.
Keywords:gas chromatography-mass spectrometry  plastic runway  diisocyanate  ultrasonic extraction  harmful substances
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