色谱 ›› 2016, Vol. 34 ›› Issue (5): 473-480.DOI: 10.3724/SP.J.1123.2016.02018

• 研究论文 • 上一篇    下一篇

高效液相色谱-串联质谱法同时测定废水中18种酚类污染物

罗碧容, 万旭, 邓星亮, 余媛媛, 谢振伟   

  1. 四川省环境监测总站, 四川 成都 610091
  • 收稿日期:2016-02-23 出版日期:2016-05-08 发布日期:2012-12-18
  • 通讯作者: 罗碧容
  • 基金资助:

    国家环境保护标准制定项目(2014-35).

Simultaneous determination of 18 phenol pollutants in waste water by high performance liquid chromatography- tandem mass spectrometry

LUO Birong, WAN Xu, DENG Xingliang, YU Yuanyuan, XIE Zhenwei   

  1. Sichuan Environmental Monitoring Center, Chengdu 610091, China
  • Received:2016-02-23 Online:2016-05-08 Published:2012-12-18
  • Supported by:

    Establishment item of National Standards for Environmental Protection (No. 2014-35).

摘要:

建立了上清液直接进样-高效液相色谱-串联质谱同时测定废水中18种酚类污染物的分析方法。取5.0 mL水样置于具塞离心管中,加氨水调节pH≥12,摇匀,加入1.0 mL二氯甲烷-正己烷(2: 1, v/v)混合溶液并振摇5 min, 4000 r/min离心5 min,用玻璃针筒抽取上清液并经0.22 μ m聚四氟乙烯滤膜过滤,用甲酸调节水样pH至中性;然后采用Thermo Hypersil ODS柱(100 mm×2.1 mm, 5.0 μ m)分离,以甲醇-0.01 mol/L甲酸铵-甲酸水溶液(pH 4.0)为流动相进行梯度洗脱,流速0.2 mL/min,柱温30℃,进样10 μ L,电喷雾负离子电离(ESI-)模式、多反应监测(MRM)模式进行检测,外标法定量。18种酚类化合物的峰面积与其质量浓度在一定浓度范围内均呈良好的线性关系(r2≥0.9991),方法检出限为0.10~0.88 μ g/L。测定低、中、高加标浓度的样品,18种酚类化合物的相对标准偏差为2.5%~9.9%(n=6);火工药剂废水与石油化工废水样品中的平均加标回收率为68.7%~118%(n=3)。此方法操作简单,灵敏度高,干扰小,分析速度快,可适用于环境废水中18种酚类污染物的同时分析。

关键词: 废水, 酚类污染物, 高效液相色谱-串联质谱法

Abstract:

A method was developed for the simultaneous determination of 18 phenol pollutants in waste water by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). A volume of 5.0 mL waste water was placed into a centrifuge tube. Ammonia was added to the waste water to adjust pH≥12. A volume of 1.0 mL methylene chloride-hexane solution (2: 1, v/v) was added to the waste water, then the centrifuge tube was oscillated for 5 min and centrifuged for 5 min at 4000 r/min. The water sample was filtered through a 0.22 μ m polytetrafluoroethylene (PTFE) microfiltration membrane and adjusted to neutral by formic acid. With methanol-0.01 mol/L ammonium formate/formic acid aqueous solution (pH 4.0) as mobile phase, the separation was performed on a Thermo Hypersil ODS column (100 mm×2.1 mm, 5.0 μ m) in gradient elution. The flow rate was 0.2 mL/min. The column temperature was 30℃. The samples were detected by multiple reaction monitoring (MRM) mode with negative electrospray ionization. The phenol pollutants were quantified by external standard method. The calibration curves of the phenol pollutants showed good linearities in a suitable range with correlation coefficients (r2) not less than 0.9991. The detection limits of phenol pollutants ranged from 0.10 μ g/L to 0.88 μ g/L. The relative standard deviations of phenol pollutants were 2.5%-9.9% (n=6). The average recoveries of the 18 phenol pollutants spiked in waste water samples ranged from 68.7% to 118%(n=3). The method has been proven to be sensitive, rapid and little interference. It is suitable for the determination of the 18 phenol pollutants simultaneously in environmental waste water.

Key words: high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), phenol pollutants, waste water

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