Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense M, Denmark.
Rapid Commun Mass Spectrom. 2022 Aug 30;36(16):e9339. doi: 10.1002/rcm.9339.
The type and quantity of environmentally problematic disinfection byproducts (DBPs) produced during chlorination of water depend on the natural organic matter and organic contaminants that raw water contains, and on the operational conditions of the drinking water treatment process. There is a need for a fast and quantitative method that determines which DBPs are produced and monitors the chemical dynamics during a drinking water treatment.
A small experimental chemical reactor (50 mL) was mounted directly onto the membrane inlet interface of a membrane inlet mass spectrometer (MIMS). In this setup, the membrane was the only separation between the reaction mixture in the chemical reactor and the open ion source of the mass spectrometer 2 cm away. Water samples to be chlorinated were placed in the reactor and the chlorination reaction was initiated by injection of hypochlorite. The formation of intermediates and products was monitored using either full-scan mass spectra or selected ion monitoring of relevant ions.
An algorithm for analyte quantification was successfully developed for analysis of the complex mixtures of phenol (a model for waterborne organic compounds), chlorinated intermediates and trihalomethane products which simultaneously pass the membrane into the mass spectrometer. The algorithm is based upon the combined use of standard addition and an internal standard, and all analytes could be quantified at nanomolar concentrations corresponding to realistic water treatment conditions. Experiments carried out in the temperature range 15-60°C showed that the reaction dynamics change with operational parameters, for example in tap versus deionized water.
We have successfully shown that an experimental laboratory reactor directly interfaced with a MIMS can be used for quantitative monitoring of the chemical dynamics during a water treatment. This technique could provide rapid assistance in the optimization of operating parameters for minimizing DBP production.
在对水进行氯化消毒时,产生的环境问题消毒副产物(DBP)的类型和数量取决于原水中的天然有机物和有机污染物,以及饮用水处理工艺的运行条件。因此,需要有一种快速定量的方法来确定产生了哪些 DBP,并监测饮用水处理过程中的化学动力学。
一个小型实验化学反应器(50 毫升)直接安装在膜进样接口质谱仪(MIMS)上。在这种设置中,膜是反应混合物在化学反应器和距离质谱仪 2 厘米的开放离子源之间的唯一分离物。要氯化的水样被放置在反应器中,通过注入次氯酸盐来引发氯化反应。通过全扫描质谱或相关离子的选择离子监测来监测中间产物和产物的形成。
成功地为分析酚(一种水载有机化合物的模型)、氯化中间体和三卤甲烷产物的复杂混合物开发了一种分析物定量算法,这些混合物同时通过膜进入质谱仪。该算法基于标准添加和内标物的联合使用,所有分析物都可以在纳摩尔浓度下进行定量,这对应于实际的水处理条件。在 15-60°C 的温度范围内进行的实验表明,反应动力学随操作参数而变化,例如在自来水和去离子水中。
我们已经成功地表明,与 MIMS 直接接口的实验实验室反应器可用于定量监测水处理过程中的化学动力学。这项技术可以为优化操作参数以最小化 DBP 生成提供快速帮助。