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1.
Sensors (Basel) ; 23(7)2023 Mar 30.
Article in English | MEDLINE | ID: mdl-37050676

ABSTRACT

Particle mass and particulate size are two important parameters used to characterize the aerosol. Currently, there are a few methods for measuring particle mass concentration and particle size. However, the existing methods have their own shortcomings. In this article, we describe a novel laser scattering instrument that measures mass concentration and particle size in real time over a wide concentration range. This instrument combines laser scattering and time-of-flight aerodynamics in one optical device. There are two innovations in this paper: (1) Two APD detectors are used to receive scattered light. One receives forward-scattered light and the other receives side-scattered light. The advantage is that the sensitivity of the detector is increased greatly, and the ratio of forward and side scattering is used to further obtain the size and shape information of the particles. (2) In order to measure the high concentrations of aerosol, a high-speed ADC and FPGA is combined to achieve an anti-overlap algorithm objective. It has been verified by experiments that the anti-overlapping algorithm can effectively improve the applicability of the aerodynamic particle size spectrometer under high concentration conditions.

2.
ACS Appl Mater Interfaces ; 13(43): 51535-51545, 2021 Nov 03.
Article in English | MEDLINE | ID: mdl-34672528

ABSTRACT

Efficient capture of benzoylurea insecticide (BU) residue in food is a vital procedure for food safe monitoring. Herein, a core-shell structured magnetic fluorinated covalent organic framework with good magnetic responsiveness and abundant fluorine affinity sites was successfully synthesized, suitable for magnetic solid-phase extraction (MSPE) of BUs. Using a room-temperature synthesis strategy, the magnetic fluorinated covalent organic framework was fabricated by in situ polymerization of 1,3,5-tris(4-aminophenyl) triazine (TAPT) and 2,3,5,6-tetrafluoroterephthaldehyde (TFTA) on the surface of carboxylated Fe3O4 nanoparticles. The competitive adsorption experiment and molecular simulation verified that this magnetic fluorinated covalent organic framework possesses favorable adsorption affinity for BUs. This magnetic fluorinated covalent organic framework could be easily regenerated and reused at least eight times with no reduction of enrichment performance. Combining this magnetic fluorinated covalent organic framework-based MSPE with high-performance liquid chromatography-tandem mass spectrometry, a novel sensitive method for the analysis of BUs was developed. In yellow wine and fruit juice samples, good linear correlations were obtained for BUs in the range of 10-2000 and 20-4000 ng·L-1, respectively. The limit of quantitation of the BUs ranged from 1.4 to 13.3 ng·L-1 in the two beverage matrices. Desirable precision was achieved, with intraday and interday relative standard deviations lower than 11%.


Subject(s)
Aldehydes/chemistry , Beverages/analysis , Food Analysis , Pesticide Residues/analysis , Phenylurea Compounds/analysis , Solid Phase Extraction , Triazines/chemistry , Aldehydes/chemical synthesis , Food Analysis/instrumentation , Halogenation , Magnetic Phenomena , Molecular Structure , Solid Phase Extraction/instrumentation , Triazines/chemical synthesis
3.
Food Chem ; 345: 128749, 2021 May 30.
Article in English | MEDLINE | ID: mdl-33302110

ABSTRACT

The development of sensitive method for analysis ofpesticide residue is of great significance to ensure food safety and promote globalization of food trade. An original method was proposed for analysis of phenoxy carboxylic acids (PCAs) pesticide in plant-derived food. To concentrate trace PCAs, the TAPT-DHTA-COF was fabricated by a facile room-temperature method and utilized as the solid phase extraction cartridge packing. The TAPT-DHTA-COF exhibited excellent adsorption capacity and recyclability towards PCAs. Theoretical simulation indicated that the adsorption of PCAs onto the TAPT-DHTA-COF was driven by hydrogen bond, halogen bond and π-π interaction. Using liquid chromatography tandem mass spectrometry for detection, good linearity ranged from 0.10 to 40 ng·g-1 and low limits of detection varied from 0.007 to 0.030 ng·g-1 were achieved for PCAs in rice, apple and greengrocery. The recoveries of PCAs from the spiked samples ranged from 81.2% to 107%. The reliability was verified by the accurate determination of certified reference materials.


Subject(s)
Carboxylic Acids/analysis , Food Analysis/methods , Food Contamination/analysis , Hydroxyl Radical/chemistry , Metal-Organic Frameworks/chemistry , Pesticide Residues/analysis , Plants, Edible/chemistry , Adsorption , Carboxylic Acids/chemistry , Carboxylic Acids/isolation & purification , Chromatography, Liquid , Limit of Detection , Pesticide Residues/chemistry , Pesticide Residues/isolation & purification , Reproducibility of Results , Solid Phase Extraction , Tandem Mass Spectrometry
4.
Anal Chim Acta ; 1126: 82-90, 2020 Aug 22.
Article in English | MEDLINE | ID: mdl-32736728

ABSTRACT

The facile fabrication of covalent organic frameworks (COFs) is significant for exploring and promoting their application. In this study, TAPA-TFPB-COFs with flower-shaped morphology, good crystallinity, and high surface area was prepared via a facile room-temperature method. The as-synthesized TAPA-TFPB-COFs exhibited great adsorption capacity towards quinolone antibiotics (QAs) and satisfying reusability. Utilizing the TAPA-TFPB-COFs as solid-phase extraction cartridge packing and liquid chromatography-tandem mass spectrometry as detector, a reliable and ultrasensitive method for the assay of QAs was developed. The linearity ranges of QAs extended from 0.5 to 200 ng L-1 with correlation coefficients higher than 0.9974, and the limits of detection varied from 0.02 to 0.11 ng L-1. The intra-day and inter-day precision were lower than 10.8% and 6.7%, respectively. The applicability of the developed method was evaluated through analyzing of tap water, spring water, chicken, and fish samples. The recoveries of QAs in spiked water and food samples varied from 80.0% to 107.6%. The reliability of the developed method was further verified by the accurate detection of QAs in a fish certified reference material.


Subject(s)
Metal-Organic Frameworks , Quinolones , Animals , Anti-Bacterial Agents , Chromatography, High Pressure Liquid , Limit of Detection , Reproducibility of Results , Solid Phase Extraction , Temperature
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