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机构地区:[1]中国石化石油化工科学研究院,北京100083
出 处:《石油学报(石油加工)》2015年第5期1103-1109,共7页Acta Petrolei Sinica(Petroleum Processing Section)
基 金:国家重点基础研究发展计划"973"项目(2012CB224800)基金资助
摘 要:利用选择反应监测模式(SRM),建立了一种快速、灵敏的深度加氢脱硫柴油中二苯并噻吩类化合物(DBTs)的气相色谱-三重四级杆质谱(GC-QQQ-MS/MS)测定方法。以5种DBTs混合标样绘制标准曲线,对深度加氢柴油中的C0~C4烷基取代二苯并噻吩((C0~C4)DBTs)进行定量。实验结果表明,采用该方法可以避免柴油中其他化合物的干扰,快速准确测定深度加氢脱硫柴油中(C0~C4)DBTs的含量,而且重现性好,相对标准偏差低于10%,方法的线性相关系数R2〉0.9996,检出限和定量限分别在0.0006~0.0017mg/L和0.002~0.006mg/L范围,回收率在98.23%~114.59%范围。该方法适用于深度加氢脱硫柴油中DBTs的测定。An efficient and sensitive analytical method of gas chromatography-triple quadrupole mass spectrometry(GC-QQQ-MS/MS)with the selected reaction monitoring(SRM)for determination of dibenzothiophenes(DBTs)in deep hydrodesulfurized diesel was developed.The standard curves of DBTs were figured out,and the DBSs with alkyl chains of0 to 4carbon atoms((C0-C4)DBTs)in deep hydrodesulfurized diesel were analyzed quantitatively.The experimental data showed that the matrix interference during the determination of(C0-C4)DBTs could be effectively eliminated,and the(C0-C4)DBTs in deep hydrodesulfurized diesel could be rapidly and sensitivily determined by this method with the relative standard deviation of less than 10%and the linear correlation coefficients of more than 0.9996(R20.9996).For all(C0-C4)DBTs the detection limit(LOD)and quantitation limit(LOQ) were in the ranges of 0.0006- 0.0017 mg/L and 0.002-0.006mg/L,respectively,and the recoveries were in the range of 98.23%-114.59%.This method is suitable for the determination of DBTs in deep hydrodesulfurized diesel.
关 键 词:二苯并噻吩类化合物 气相色谱-三重四级杆质谱 柴油 选择反应监测 深度加氢脱硫
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