Characteristics, influence factors, and health risk assessment of volatile organic compounds through one year of high-resolution measurement at a refinery.

From January 2020 to December 2020, high-resolution data of volatile organic compound (VOC) concentrations were monitored by online instruments at a petroleum refinery. The measurement results showed that the external contaminants, meteorological conditions and photochemical reactions had a great influence on the VOC data measured in the petroleum refineries. Some significant differences were observed in the emission composition of different refineries, while propene (34.2%), propane (10.2%), n-butane (5.6%), i-pentane (5.0%) were the dominant species emitted from the refinery in this study. The correlations between compounds with similar atmospheric lifetimes were strong (R2 > 0.9), which indicated that the diagnostic ratios of these compounds could be used as indicators to identify the refinery emission source. Chronic health effects of non-carcinogenic risk results showed that acrolein had the highest non-carcinogenic risk and other compound-specific health risks may be of less concern in the refining area. Halogenates and aromatics accounted for 97.4% of the total carcinogenic risk values, while 1,2-dibromoethane, chloromethane, benzene, trichloromethane, 1,2-dichloroethane contributed approximately 80% of the total carcinogenic risk assessment values. This research has recorded valuable data about the VOC emission characteristics from the perspective of the high-resolution monitoring of the petroleum refinery. The results of this work will provide a reference to accurately quantify and identify the emission of petroleum refineries and further throw some light on effective VOC abatement strategies.

Quantum-Dot-Based Lateral Flow Immunoassay for Detection of Neonicotinoid Residues in Tea Leaves.

Neonicotinoid insecticides are commonly used for pest control on tea plantations as a result of their broad-spectrum activity. However, neonicotinoid residues released from tea leaves into tea infusions pose a dietary risk to consumers. Therefore, a rapid, sensitive, and reliable on-site detection method for neonicotinoids is needed. We developed a quantum-dot-based fluorescent lateral flow immunochromatographic strip (LFICS) combined with a broad-specific antibody for detection of typical neonicotinoids (imidacloprid, imidaclothiz, and clothianidin), with sensitivities [50% inhibitory concentration (IC50)] of 0.104-0.33 ng/mL and visual detection limits of 0.5-1 ng/mL. The strip assay could be completed in less than 30 min. Using the LFICS to analyze spiked tea samples (green tea, black tea, and oolong tea), the average recovery of the three neonicotinoids ranged between 71 and 111%, with the coefficient of variation below 12%. The results from the LFICS tests for field samples were consistent with results from ultraperformance liquid chromatography-tandem mass spectrometry. The newly developed strip is a useful tool for the on-site detection of neonicotinoid residues in tea.

Enzyme-linked immunosorbent assay for the determination of five organophosphorus pesticides in camellia oil.

A matrix solid-phase dispersion and direct competitive enzyme-linked immunosorbent assay (MSPD-ELISA) was developed for five organophosphorus pesticides (OPs) in camellia oil. Seven haptens with different substituents in the aromatic ring were used to prepare different competitors; the ELISA showed highest sensitivity and specificity to OPs when the competitor had moderate heterology to the immunizing hapten. Several assay conditions were optimized to increase the ELISA sensitivity. The optimized ELISA for five OPs had 50% inhibitory concentrations of 6.3 ng/ml (parathion), 18.9 ng/ml (methyl parathion), 120.7 ng/ml (fenitrothion), 110.4 ng/ml (fenthion), and 20.7 ng/ml (phoxim). The average recoveries of five OPs in camellia oil ranged from 75.7 to 105.3%, with the interassay coefficient of variations ranging from 6.0 to 13.4%. Compared with the results previously reported, the ELISA that was developed in the present study showed a much higher sensitivity. Additionally, MSPD was used in the sample preparation to minimize the matrix effect. Recoveries from the method developed here were in agreement with those obtained by gas chromatography, which indicated that the detection performance of the MSPD-ELISA could meet the regulatory requirements of different governments and international organizations.