职业与健康 ›› 2023, Vol. 39 ›› Issue (6): 760-763.

• 论著 • 上一篇    下一篇

连续流动分析仪同时测定生活饮用水中挥发酚、氰化物、阴离子合成洗涤剂和硫化物含量

邹柯婷1, 巩胜利2, 赵桂鹏1, 何丰瑞1, 程训强3, 秦国富1   

  1. 1.西安市疾病预防控制中心理化检验科,陕西 西安 710054;
    2.武警甘肃省总队医院医学影像科,甘肃 兰州 730000;
    3.上海宝中盈仪器仪表有限公司,上海 201108
  • 收稿日期:2022-06-29 修回日期:2022-08-01 发布日期:2026-03-04
  • 通信作者: 秦国富,主管技师,E-mail:qinguofu123@126.com
  • 作者简介:邹柯婷,女,工程师,主要从事食品安全检测与药物分析工作。
  • 基金资助:
    陕西省重点研发计划项目(2021SF-468); 西安市卫生健康委一般研究项目(2020yb45)

Simultaneous determination of volatile phenol,cyanide,anionic synthetic detergent and sulfide in drinking water by continuous flow analyzer

ZOU Ke-ting1, GONG Sheng-li2, ZHAO Gui-peng1, HE Feng-rui1, CHENG Xun-qiang3, QIN Guo-fu1   

  1. 1. Physical and Chemical Laboratory,Xi'an Center for Disease Control and Prevention,Xi'an Shaanxi 710054,China;
    2. Medical Imaging Department,Gansu Provincial Armed Police Corps Hospital,Gansu Lanzhou 730000,China;
    3. Shanghai Baozhongying Instrument Co.,Ltd,Shanghai 201108,China
  • Received:2022-06-29 Revised:2022-08-01 Published:2026-03-04
  • Contact: QIN Guo-fu,Technician,E-mail:qinguofu123@126.com

摘要: 目的 建立连续流动分析仪同时测定生活饮用水中挥发酚、氰化物、阴离子合成洗涤剂和硫化物的方法。方法 采用在线蒸馏,馏出物在碱性铁氰化钾存在下与4-氨基安替比林反应,利用分光光度法测定挥发酚的含量,采用在线蒸馏,馏出物与氯胺-T反应,再与异烟酸-吡唑酮反应生成蓝色化合物,利用分光光度法测定氰化物的含量,在线萃取,利用亚甲蓝分光光度法测定阴离子合成洗涤剂的含量,利用硫离子与N,N-二甲基对苯二胺二盐酸盐反应生成蓝色化合物进行测定硫化物含量。结果 挥发酚与氰化物在质量浓度为2~100 μg/L时,线性相关系数r≥0.999 9,检出限分别为0.2和0.4 μg/L,相对标准偏差分别为0.75%~2.80%和0.36%~2.26%,加标回收率为98.0%~103.6%和101.0%~102.0%。阴离子合成洗涤剂与硫化物在质量浓度为20~1 000 μg/L时,线性相关系数为0.999 5和0.999 9,检出限分别为4.4和1.6 μg/L,相对标准偏差为0.55%~1.08%和0.33%~1.97%,加标回收率为93.6%~95.8%和99.0%~101.9%。与国家标准方法相比,差异无统计学意义(P>0.05)。结论 所建立的方法比国标法省时省力、检出限更低、精密度与准确度更好、污染更小,更适于大批量样品的分析测定。

关键词: 挥发酚, 氰化物, 阴离子合成洗涤剂, 硫化物, 连续流动分析仪

Abstract: Objective To establish a method for simultaneous determination of volatile phenol,cyanide,anionic synthetic detergent and sulfide in drinking water by continuous flow analyzer. Methods Using on-line distillation,the distillate reacted with 4-aminoantipyrine in the presence of basic potassium ferricyanide,and the content of volatile phenol was determined by spectrophotometry. Using on-line distillation,the distillate reacted with chloramine-T,and then reacted with isonicotinic acid pyrazolone to form blue compounds,the content of cyanide was determined by spectrophotometry. Usingon-line extraction,the content of anionic synthetic detergent was determined by methylene blue spectrophotometry,and sulfide was determined by the reaction of sulfur ion with N,N-dimethyl-p-phenylenediamine dihydrochloride. Results When the mass concentration of volatile phenol and cyanide was 2-100μg/L,the linear correlation coefficients(r) were≥0.999 9,and the detection limits were 0.2 and 0.4 μg/L respectively,the relative standard deviations were 0.75%-2.80% and 0.36%-2.26% respectively,and the recoveries were 98.0%-103.6% and 101.0%-102.0% respectively. When the mass concentration of anionic synthetic detergent and sulfide was 20-1000 μg/L,the linear correlation coefficients were 0.9995 and 0.999 9 respectively,and the detection limits were 4.4 and 1.6 μg/L respectively,the relative standard deviations were 0.55%-1.08% and 0.33%-1.97% respectively,and the recoveries were 93.6%-95.8% and 99%-101.9% respectively. Compared with the national standard method,the difference was not statistically significant. Conclusion Compared with the national standard method,this method saves time and labor,has lower detection limit,better precision and accuracy,less pollution,and is more suitable for the analysis and determination of large quantities of samples.

Key words: Volatile phenol, Cyanide, Anionic synthetic detergent, Sulfide, Continuous flow analyzer

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