An in-situ versatile screening method for identifying SVOC sources in indoor environments.

Indoor semivolatile organic compounds (SVOCs) pose a substantial threat to human health. However, identifying the sources of these emissions has been challenging owing to the scarcity of convenient and practical on-site methodologies. Herein, a novel method for source screening was proposed using aluminum silicate sampling strips to adsorb SVOCs from the surface air of indoor materials. The adsorbed SVOC levels indicate the emission intensity of these materials into indoor environments. Additionally, compact sampling strips can be readily fixed to any vertical surface using a static sticker, facilitating the characterization of various materials in practical settings. Laboratory-simulated experiments demonstrated the capability of the proposed method to differentiate between source and non-source materials within a 10-cm distance in the same space. In practical scenarios, the primary emission sources identified via this method exhibited a consistent correlation with the contents of the corresponding materials obtained from the traditional solvent-extraction method. As the adsorbed SVOCs were directly transferred to a GC-MS through thermal desorption instead of the solvent-extraction procedure, the proposed method demonstrated several-fold improvements in analytical sensitivity and efficiency. Using this versatile screening technique, some emerging and important SVOC species were identified within specific indoor materials. Eliminating these sources has been demonstrated as an effective approach to mitigate SVOC pollution. Overall, the proposed method offers a powerful tool for managing indoor pollutants and safeguarding human health.

Dust phase and window film phase phthalates in dormitories: profile characteristics, source screening, and estimated gas-phase concentration and dermal exposure comparison.

Recently, phthalate exposure has become a major public health concern. However, gaps still remain in our understanding of phthalate profile characteristics, source screening, and gas-phase estimation. This study measured phthalate concentrations in dust and window films in 101 dormitories at 13 universities in Beijing, China, from October to December 2019. Based on the phthalate concentrations in the dust and window films, we estimated the gas-phase phthalate concentrations using steady-state and instantaneous equilibrium models, respectively, and male and female students' dermal exposure using the Monte Carlo simulation. Commonly used materials and supplies were screened for phthalate sources and evaluated using the positive matrix factorization (PMF) model. The results showed that the detection frequency of ten phthalates ranged from 79.2 to 100% in dust and from 84.2 to 100% in window films. Dicyclohexyl phthalate (DCHP), di-(2-ethylhexyl) phthalate (DEHP), and dibutyl phthalate (DBP) were the most abundant phthalates in both indoor media and were also predominant in the indoor materials and supplies. The PMF results indicated that the potential sources of phthalates in dust and window films had both similarities and differences. Indoor door seals, paint, coatings, cables, air-conditioning rubber cable ties, wallpaper, and window seals were highly probable sources of phthalates. The gas-phase phthalate concentrations estimated using the two methods differed, especially for phthalates with high octanol-air partition coefficients (Koa), varying by 1-2 orders of magnitude. Moreover, compared with related studies, the gas-phase concentrations were significantly underestimated for phthalates with high Koa values, while the estimated gas-phase concentrations of phthalates with low Koa values were closer to the measured values. The estimated dermal exposure using the two methodologies also considerably differed. Such findings suggest that more attention should be focused on the exposure risk from the dust phase and window film phase phthalates.

Modulating the metal center in MIL-101 for the piezoelectric catalytic synthesis of hydrogen peroxide.

Modulation of metal centers is a promising strategy to boost catalytic performance. Two structurally identical MOFs with different metal centers, namely MIL-101(Cr) and MIL-101(Fe), were synthesized. MIL-101(Cr) exhibits superior H2O2 yield due to Cr's electron-donating ability. This work helps in developing the rational design and optimization of MOF catalysts for catalytic reactions.

Strong temperature influence and indiscernible ventilation effect on dynamics of some semivolatile organic compounds in the indoor air of an office.

Many manmade organic air pollutants are semivolatile and primarily used and exposed indoors. It remains unclear how indoor environmental parameters affect indoor air dynamics of semivolatile organic compounds (SVOCs) in real-world indoor conditions, which directly relates to human exposure. By making time-resolved SVOC measurements over multiple weeks in an office, we characterized the indoor air dynamics of six representative SVOCs which were mainly present in the gas phase and of indoor origins, and investigated the effects of the temperature and ventilation rate. The six species include di-isobutyl phthalate and di-n-butyl phthalate, as well as two n-alkanes and two siloxanes. Airborne concentrations of all six SVOCs responded strongly and quickly to changes in the indoor temperature. The temperature dependence of individual species can be well fitted in the form of the van't Hoff equation, and explained 65-86% of the observed variation in the logarithm-transformed concentrations. In contrast, increasing the ventilation rate by a factor of 3-5 for hours at a constant temperature had no discernible influence on the SVOC concentrations. Further kinetic modeling analysis suggests that the observed fast temperature response and indiscernible ventilation effect are both associated with SVOC sorption onto indoor surfaces, which dramatically slows the response of SVOC concentration to changes in the ventilation rate and speeds up the response to changes in the temperature. These results highlight the importance of sorption reservoirs on regulating indoor SVOC dynamics and also have important implications for controlling and assessing indoor air exposure to SVOCs.

Method Development for Direct Multielement Quantification by LA-ICP-MS in Food Samples.

A novel calibration strategy for the accurate determination of essential and toxic elements in both plant-based and animal-based foods was developed by synthesizing spiked agarose gels as matrix-matched external standards and carbon as the internal standard (IS). Aqueous solutions of agarose (4%, m/v) with defined amounts of the analytes were cast on a mold and then dried to form the agarose-gel standards. The spatial distributions of the analytes in the gel were examined using surface- and depth-mapping laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS) protocols, and the gel homogeneity was found to be excellent (i.e., relative standard derivation <10%). Recovery of the 19 spiked elements in the gel standards was in the range of 86.9-94.7%. The limits of detection (LODs) ranged from 0.0005 (Rb) to 33.7 µg g-1 (S). Analysis results were in good agreement with certified values for various certified reference materials (CRMs). Furthermore, a porous rubber sample supporter was developed to improve the analysis throughput by about 3-fold.

Liquid Spray Dielectric Barrier Discharge Induced Plasma-Chemical Vapor Generation for the Determination of Lead by ICPMS.

In the present study, a novel and sensitive liquid spray dielectric barrier discharge induced plasma-chemical vapor generation technique (LSDBD-CVG) is developed for the determination of lead concentration by inductively coupled plasma mass spectrometry (ICPMS). The dissolved Pb2+ is readily converted to volatile species by LSDBD plasma induced chemical processes in the presence of 5% (v/v) formic acid in a supporting electrolyte (HCl, 0.01 mol L-1). In this LSDBD approach, the sample solution is converted to aerosol and simultaneously mixed with the DBD plasma generated at the nozzle of a pneumatic nebulizer, which greatly facilitates Pb vapor generation because of the enhanced interaction of sprayed analytes and the plasma. Optimal conditions for LSDBD-CVG were identified, and the interference effects from other metal ions were assessed. Under optimized conditions, the detection limit of Pb was found to be 0.003 µg L-1. The repeatability, expressed as the relative standard deviation (RSD) of the peak height, for the five replicate measurements of 0.03 and 1 µg L-1 lead standard, were 2.1% and 1.7%, respectively. Compared with other vapor generation methods, this new LSDBD-CVG offers several advantages including no requirement of unstable reagents, fast response, and easy coupling with flow injection, along with high tolerance for coexisting ions. The accuracy of the proposed method is demonstrated by successful analysis of Pb in reference material of stream sediment (GBW07311), soil (GBW07403), basalt (BCR-2), and simulated water sample (GBW08601). The proposed LSDBD-CVG extends the scope of elements accessible by plasma-CVG and provides an alternative efficient green approach for the vapor generation of Pb.