Abstract
The misuse of pesticides poses a tremendous threat to human health. Excessive pesticide residues have been shown to cause many diseases. Many sensor detection methods have been developed, but most of them suffer from problems such as slow detection speed or narrow detection range. So, the development of rapid, direct and sensitive means of detecting trace amounts of pesticide residues is always necessary. A novel online sensor technique was developed for direct analysis of pesticides in complex matrices with no sample pretreatment. The portable sensor ion source consists of an MPT (microwave plasma torch) with desolventizing capability and an APCI (atmosphere pressure chemical ionization), which provides abundant precursor ions and a strong electric field. The performance which improves the ionization efficiency and suppresses the background signal was verified by using pesticide standard solution and pesticide pear juice solution measurements with an Orbitrap mass spectrometer. The limit of detection (LOD) and the limit of quantization (LOQ) of the method were measured by pear juice solutions that were obtained in the ranges of 0.034–0.79 μg/L and 0.14–1 μg/L. Quantitative curves were obtained ranging from 0.5 to 100 μg/L that showed excellent semi-quantitative ability with correlation coefficients of 0.985–0.997. The recoveries (%) of atrazine, imidacloprid, dimethoate, profenofos, chlorpyrifos, and dichlorvos were 96.6%, 112.7%, 88.1%, 85.5%, 89.2%, and 101.9% with the RSDs ranging from 5.89–14.87%, respectively. The results show that the method has excellent sensitivity and quantification capability for rapid and direct detection of trace pesticide.
Highlights
As a new sensor technology, mass spectrometry has been widely used in biology, medicine and the environment, etc
Laser mass spectrometry as an online sensor has great potential to be applied to industrial processes such as for the analysis of coffee roasting [1], and electrospray ionization mass spectrometry (ESI-MS) has been coupled with microdialysis sampling to perform in vivo chemical monitoring
We present a sensitive, portable and direct multi-mode ionization technique as an online sensor that integrates atmospheric pressure chemical ionization (APCI) and microwave plasma torch (MPT) sources with an Orbitrap mass spectrometer
Summary
As a new sensor technology, mass spectrometry has been widely used in biology, medicine and the environment, etc. Laser mass spectrometry as an online sensor has great potential to be applied to industrial processes such as for the analysis of coffee roasting [1], and electrospray ionization mass spectrometry (ESI-MS) has been coupled with microdialysis sampling to perform in vivo chemical monitoring. The imaging mass-spectrometry sensor is a powerful technique that allows for storing multiple time stamps in each pixel for each time-of-flight cycle to obtain more chemical information on a sample [3]. PTR-MS as a multipurpose sensor has been widely used in environmental, agri-food and health science sectors [4]. The development of new mass-spectrometry detection technology has great significance to expanding sensor application fields, such as high-sensitivity and rapid detection of complex substances
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