Benzene Series Research Articles

How the Most Neglected Residual Species in MOF-Based Catalysts Involved in Catalytic Reactions to Form Toxic Byproducts.

In recent years, multifarious new materials have been developed for environmental governance. Thereinto, metal organic framework (MOF)-based catalysts have been widely employed for heterogeneous catalysis because of their high porosity to confine noble metal particles faraway from aggregation. However, the potential reactions between residual species from the material synthesis process and target pollutants, which could form highly toxic byproducts, are often neglected. Herein, we took the widely used Zr-MOF, UiO-66, with highly thermal stability supported Pd catalysts as the example to investigate how the residual species in catalysts are involved in aromatic volatile organic compounds (VOCs) degradation reaction. The results showed that residual Cl species originated from the ZrCl4 metal precursor participated in the VOC degradation reaction, leading to the production of various chlorine-containing byproducts, even the hypertoxicity dioxin precursor, dichlorobenzene. Meanwhile, the chlorination mechanism for the formation of chlorine-containing byproducts was revealed by density functional theory calculation. Furthermore, the highly efficient residual Cl removal approaches are proposed. Importantly, the migration and transformation of residual Cl during the degradation of five benzene series VOCs are comprehensively studied and elucidated. We anticipate that these findings will raise alarm about the neglected issue of residual species in MOF-based catalysts for heterogeneous catalysis, especially environmentally friendly catalysis.

Determination of multiple restricted and prohibited ingredients in hair dyes using a novel 3D stationary phase coupled with gas chromatography-mass spectrometry

Hair dyes (HDs) are mainly composed of various benzene series, amines, and phenolic compounds. These ingredients are well known to have allergenic, teratogenic, and carcinogenic properties. As such, the presence of these ingredients in HDs has received increased attention in recent years. At present, the applications of traditional analytical and detection methods and commercial chromatographic columns are limited by problems such as poor qualitative analysis and inaccurate quantification. Thus, the development of new analytical and detection technologies and stationary phases is an urgent endeavor. Moreover, HDs contain complex compounds and exhibit significant matrix interference. Hence, appropriate sample pretreatment methods are necessary to analyze HDs. In this study, the 3D nonpolar rigid structure of triptycene (TP) was combined with the polar flexible chains of polyethylene glycol (PEG) to design and synthesize a TP derivative, TP-PEG, as a stationary phase for chromatographic columns. The stationary phase enabled the expansion of the selection range for polar and nonpolar analytes. Subsequently, gas chromatography-mass spectrometry (GC-MS) was used to quantitatively analyze 22 ingredients in HDs. The experimental results demonstrated that analytes with different polarities exhibited sharp and symmetrical peak shapes on the stationary phase, and all 22 analytes achieved baseline separation on the chromatographic column. The 22 ingredients in HDs showed good linear relationships within their respective ranges, with correlation coefficients greater than 0.9985. The average recovery rates at three spiked levels were in the range of 89.2%-103.2%, and RSDs were less than 5%. Compared with traditional methods, the proposed method has higher efficiency and better accuracy, thus verifying the excellent separation performance of the new stationary phase and the effectiveness of the established GC-MS detection method. The findings indicated the applicability of the developed method to the detection and analysis of various compounds in HDs.

Transmission of substituent effects in para-disubstituted benzenes: 13C chemical shift and Mulliken charge modeling of para carbon atoms via the Reynolds DSP model

The PM3 calculations of the Mulliken charge and the experimental 13C substituent chemical shifts (SCS) of para carbon for 17 para-disubstituted benzene series were investigated by correlation analysis. A significant correlation between the charge and the 13C SCS of the para carbon of the same series was observed. In mono-substituted benzene, the correlation of para13C SCS with Mulliken charges calculated by PM3 and Mulliken charge calculated by DFT(B3LYP) with basis set 6 311(dp)G of the same carbon is similar. All the substituent effects on the charge and 13C SCS were modeled by the Reynolds’ dual substituent parameter model (charge or 13C SCS = ρF σF + ρRσRo), where σF and σRo are the Reynolds’ field and resonance constants, respectively, and ρF and ρR are the field and resonance effects, respectively. The coefficients of determination for all series were significant. The concept of π-polarization was used to analyze variation in ρF. The interpretation of ρF showed parallels between the charge and 13C SCS. An enhanced ρF for a given series was attributed to the stabilization of the π-polarization charge at the para carbon. The ρR was a function of extended conjugation within the side chain. Parallelism of charge and 13C SCS of the ρR of the compared series were also observed, except in series with the reverse-substituent effect and the possession of a strong electronegative group, such as a nitro or azo group.

Distribution and Risk Assessment of VOCs in Road Dust Across Different Urban Areas

ABSTRACT Volatile organic compounds (VOCs) are significant pollutants in urban road dust, but their distribution and associated health risks remain unclear. VOC distribution in road dust from six distinct urban areas in Beijing Daxing District, China was systematically investigated. Eighteen VOCs were detected, with the highest load in commercial areas (7.73 μg/g), followed by industrial parks (6.38 μg/g), residential areas (3.35 μg/g), leisure areas (2.79 μg/g), traffic areas (2.01 μg/g) and urban-rural fringe (1.85 μg/g), much lower than in air and water phases. Typical VOCs in road dust include methyl tertiary butyl ether (MTBE) (0.82–1.24 μg/g), benzene series compounds (0.02–4.19 μg/g) and volatile halogenated alkanes (0.002-0.095 μg/g). Incomplete combustion of road vehicle fuels is the key source of VOCs. Particular attention was given to VOCs in typical sites within the urban-rural fringe, known for their unique pollution characteristics. The VOCs loads were ranked as follows: Gas Stations (2.61–2.62 μg/g) > Intersection (1.41 μg/g) > Main Road (1.34 μg/g) > University Gate (1.27 μg/g). Increased vehicle activity and frequent stalling contribute to higher VOCs accumulation in road dust. Health risk assessment indicates there is no appreciable non-carcinogenic risk associated with exposure to road dust VOCs. Further research should consider VOCs in the broader environmental context, including air and water.

Toxicity of soil leaching liquor from coking plant in developmental zebrafish embryos/larvae model.

The coking industry in China is the largest coke supplier in the world. Contaminated soil in industrial areas poses a serious threat to human and ecosystems. Most of the studies investigated the toxicity of soil from coking plant on soil microorganisms, while the toxic effects of soil leaching liquor on aquatics are limited. In this study, the composition of soil leaching liquor from a coking plant in Taiyuan (TY) was analyzed, and the developmental toxicity on zebrafish was evaluated. The results showed that a total of 91 polycyclic aromatic hydrocarbons were detected in the leaching liquor, followed by phenols and benzene series. The leaching liquor induced developmental impairment in zebrafish larvae, including delayed incubation, deficits in locomotor behavior, vascular and cardiac dysplasia, and impaired neurodevelopment. The results of metabolomics analysis showed that TY soil leaching liquor induced significant metabolic profile disturbances in zebrafish embryos/larvae. The developmental toxicity of the leaching liquor metabolic disorders may be associated with the leaching liquor-induced abnormalities in zebrafish embryonic development. Metabolic pathways were identified by arginine and proline metabolism, phosphotransferase system, starch and sucrose metabolism, steroid biosynthesis, beta-alanine metabolism, and nucleotide metabolism pathways.

Hollow Fiber Sensors with a Turn-On Fluorescence Response, Recycling, and Water Proofing for Monitoring Benzene Series

Hollow Fiber Sensors with a Turn-On Fluorescence Response, Recycling, and Water Proofing for Monitoring Benzene Series

Oxygen Vacancy Enabled Electronic Structure Engineering of Pt-WO3 Nanosheets toward Highly Efficient BTEX Sensing.

A Pt nanoparticle-immobilized WO3 material is a promising candidate for catalytic reactions, and the surface and electronic structure can strongly affect the performance. However, the effect of the intrinsic oxygen vacancy of WO3 on the d-band structure of Pt and the synergistic effect of Pt and the WO3 matrix on reaction performance are still ambiguous, which greatly hinders the design of advanced materials. Herein, Pt-decorated WO3 nanosheets with different electronic metal-support interactions are successfully prepared by finely tuning the oxygen vacancy structure of WO3 nanosheets. Notably, Pt-modified WO3 nanosheets annealed at 400 °C exhibit excellent benzene series (BTEX) sensing performance (S = 377.33, 365.21, 348.45, and 319.23 for 50 ppm ethylbenzene, benzene, toluene, and xylene, respectively, at 140 °C), fast response and recovery dynamics (10/7 s), excellent reliability (σ = 0.14), and sensing stability (φ = 0.08%). Detailed structural characterization and DFT results reveal that interfacial Ptδ+-Ov-W5+ sites are recognized as the active sites, and the oxygen vacancies of the WO3 matrix can significantly affect the d-band structure of Pt nanoparticles. Notably, Pt/WO3-400 with improved surface oxygen mobility and medium electronic metal-support interaction facilitates the activation and desorption of BTEX, which contributes to the highly efficient BTEX sensing performance. Our work provides a new insight for the design of high-performance surface reaction materials for advanced applications.

Simultaneously enhancing toluene adsorption and regeneration process by hierarchical pore in activated coke: a combined experimental and adsorption kinetic modeling study.

Activated coke is a type of commonly used adsorbent for benzene series VOCs such as toluene, but traditional microporous activated coke usually faces the challenge of poor regeneration performance. Herein, based on self-made activated cokes with typical pore configuration, we found that adsorption and regeneration of toluene can be simultaneously enhanced by constructing hierarchical pore in activated coke. Correlations of pore configuration with toluene adsorption capacity and regeneration efficiency reveal that micropore contributes for strong toluene adsorption; meso-macropore provides mass transfer channel for toluene desorption and regeneration process. Hierarchical porous activated coke prepared from Zhundong subbituminous coal not only achieves the highest toluene adsorption capacity of 340.92mg·g-1, but also can retain more than 90% of initial adsorption capacity after five adsorption-regeneration cycles. By contrast, micropore-dominant activated cokes can only retain 70% of initial adsorption capacity. Adsorption kinetic modelling on adsorption breakthrough curves shows that hierarchical porous activated coke prepared from Zhundong subbituminous coal exhibits high adsorption and diffusion rate constants of 14.39 and 33.45min-1, respectively, much higher than those of micropore-dominant activated cokes. Due to the accelerated surface adsorption and diffusion processes induced by meso-macropore, toluene adsorption and regeneration behavior can be simultaneously improved. Results from this work validated the role of pore hierarchy in toluene adsorption-regeneration process, providing guidance for designing high-performance activated coke with synergistically improved toluene adsorption capacity and regeneration performance.

A microchip gas chromatography column assembly with a 3D metal printing micro column oven and a flexible stainless-steel column

In this work, a microchip gas chromatography (GC) column assembly utilizing a three-dimensional (3D) printed micro oven and a flexible stainless steel capillary column was developed. The assembly's performance and separation capabilities were characterized. The key components include a 3D printed aluminum plate (7.50 × 7.50 × 0.16 cm) with a 3-meter-long circular spiral channel, serving as the oven, and the column coiled on the channel with an inner diameter of 320 μm and a stationary phase of OV-1. A heating ceramic plate was affixed on the opposite side of the plate. The assembly weighed 40.3 g. The design allows for easy disassembly, or stacking of heating devices and columns, enabling flexibility in adjusting column length. When using n-C13 as the test analyte at 140 °C, a retention factor (k) was 8.5, and 7797 plates (2599 plates/m) were obtained. The assembly, employing resistance heating, demonstrated effective separation performance for samples containing alkanes, aromatics, alcohols and ketones, with good reproducibility. The reduction in theoretical plates compared to oven heating was only 2.95 %. In the boiling point range of C6 to C18, rapid temperature programming (120 °C/min) was achieved with a power consumption of 119.512 W. The assembly was successfully employed to separate benzene series compounds, gasoline and volatile organic compounds (VOCs), demonstrating excellent separation performance. This innovative design addresses the challenges of the complexity and low repeatability of the fabrication process and the high cost associated with microchip columns. Furthermore, its versatility makes it suitable for outdoor analysis applications.

Chlorination mechanism of benzene series in aqueous system under the combined action of Cl- and multiple free radicals

In this study, non-targeted analysis revealed that the Fe2+/perodisulfate/Cl- system degraded aniline (AN) and nitrobenzene (NB), yielding 7 types and 4 types of aromatic chlorides, respectively. In order to explore their chlorination mechanism and the influence of different functional groups, various reactions (radical adduct formation (RAF), hydrogen atom abstraction (HAA) and single electron transfer (SET)) of benzene series with various functional group with sulfate radical (SO4·-), hydroxyl radical (·OH), chlorine radical (·Cl) and dichloride anion radicals (Cl2·-) were explored by Gibbs free energy (ΔG), and the subsequent reactions of SET and HAA products (organic free radical) were innovatively explored by ΔG. This study revealed that the reaction between benzene compounds containing electron-donating groups and ·Cl was dominated by HAA rather than RAF; the reaction between benzene compounds containing electron-withdrawing groups and ·Cl was dominated by RAF. Aromatic compounds containing electron-donating groups can undergo SET reaction and generate aromatic chlorides in the presence of O2 and Cl-. Combined with the product analysis, it was found that the HAA reaction of aromatic compounds will lead to the obvious formation of biphenyl compounds and aromatic chlorides in the presence of Cl-. Compared with the conditions of RAF of ·Cl and chlorination of SET products, the chlorination reaction between HAA products and Cl- is ubiquitous, which is more likely to be the key to the formation of aromatic chlorides in mixed systems. This study provides a theoretical basis for further study on the formation risk of chlorinated products in advanced oxidation process.

Fostering a Holistic Understanding of the Full Volatility Spectrum of Organic Compounds from Benzene Series Precursors through Mechanistic Modeling.

A comprehensive understanding of the full volatility spectrum of organic oxidation products from the benzene series precursors is important to quantify the air quality and climate effects of secondary organic aerosol (SOA) and new particle formation (NPF). However, current models fail to capture the full volatility spectrum due to the absence of important reaction pathways. Here, we develop a novel unified model framework, the integrated two-dimensional volatility basis set (I2D-VBS), to simulate the full volatility spectrum of products from benzene series precursors by simultaneously representing first-generational oxidation, multigenerational aging, autoxidation, dimerization, nitrate formation, etc. The model successfully reproduces the volatility and O/C distributions of oxygenated organic molecules (OOMs) as well as the concentrations and the O/C of SOA over wide-ranging experimental conditions. In typical urban environments, autoxidation and multigenerational oxidation are the two main pathways for the formation of OOMs and SOA with similar contributions, but autoxidation contributes more to low-volatility products. NOx can reduce about two-thirds of OOMs and SOA, and most of the extremely low-volatility products compared to clean conditions, by suppressing dimerization and autoxidation. The I2D-VBS facilitates a holistic understanding of full volatility product formation, which helps fill the large gap in the predictions of organic NPF, particle growth, and SOA formation.

Ordered mesoporous hairbrush-like nanocarbon assembled microfibers for solid-phase microextraction of benzene series in oilfield sewage.

The development of advanced functional nanomaterials for solid-phase microextraction (SPME) remains an imperative aspect of sample pretreatment. Herein, we introduce a novel SPME fiber consisting of graphene fibers modified with ordered mesoporous carbon nanotubes arrays (CNTAs) tailored for the determination of benzene series in oilfield wastewater, which is synthesized by an ionic liquid-assisted wet spinning process of graphene nanosheets, followed by a precisely controlled growth of metal-organic framework and subsequent pyrolysis treatment. The resulting robust microfiber structure resembles a "hairbrush" configuration, with a crumpled graphene fiber "stem" and high-order mesoporous CNTAs "hairs". This unique architecture significantly enhances the SPME capacity, as validated by gas chromatography-mass spectrometry. The hairbrush-like nanocarbon assembled microfibers possess structural characteristics, a high specific surface area, and numerous binding sites, offering efficient enrichment of benzene series compounds in oilfield wastewater, including benzene, ethylbenzene, m-xylene, p-xylene, and toluene. Our analysis demonstrates that these microfibers exhibit broad linear ranges (0.2-600μg L-1), low detection limits (0.005-0.03mg L-1), and excellent repeatability (3.2-5.5% for one fiber, 2.1-6.7% for fiber-to-fiber)for detection. When compared to commercial alternatives, these hairbrush-like nanocarbon-assembled microfibers exhibit significantly enhanced extraction efficiency for benzene series compounds.

Study on the effect of residential interior decoration on children’s respiratory diseases: A field trial conducted in Chongqing, China

Pollutants such as formaldehyde, benzene series compounds and total volatile organic compounds (TVOC) released by residential interior decoration activities (including household renovation and new furniture) pose a severe threat to children’s respiratory health. To study the effect of indoor decoration on children’s respiratory diseases and provide suggestions to prevent it, we conducted a cross-sectional questionnaire survey amongst 6547 preschoolers from 34 kindergartens in Chongqing, China, and selected 39 houses to measure their indoor air pollutants concentrations. The results showed that household decoration, during pregnancy and early childhood, would increase the risk of children’s rhinitis, asthma and pneumonia. Vacancy time after the completion of decoration, furniture pieces and decoration materials significantly affected the concentration of formaldehyde, xylene and TVOC, which could pose a potential risk to children’s respiratory health. The concentration of xylene and TVOC and the incidence of children’s asthma and pneumonia were both negatively correlated with the vacancy time. Decoration materials such as composite and ceramic tile/stone/cement flooring and water-based/latex/oil-based paints emit more gaseous pollutants than solid wood flooring and wallpaper, respectively, which were more likely to increase the risk of children’s respiratory diseases. Adequate ventilation and air purification can reduce the impact of home decoration.

Optimizing carbon sources regulation in the biochemical treatment systems for coal chemical wastewater: Aromatic compounds biodegradation and microbial response strategies

The complex composition of coal chemical wastewater (CCW), marked by numerous highly toxic aromatic compounds, induces the destabilization of the biochemical treatment system, leading to suboptimal treatment efficacy. In this study, a biochemical treatment system was established to efficiently degrade aromatic compounds by quantitatively regulating the dosage of co-metabolized substrates (specifically, the chemical oxygen demand (COD) Glucose: COD Sodium acetate = 3:1, 1:3, and 1:1). The findings demonstrated that the system achieved optimal performance under the condition that the ratio of COD Glucose to COD Sodium acetate was 3:1. When the co-metabolized substrate was added to the system at an optimal ratio, examination of pollutant removal and cumulative effects revealed that the removal efficiencies for COD and total organic carbon (TOC) reached 94.61 % and 86.40 %, respectively. The removal rates of benzene series, nitrogen heterocyclic compounds, polycyclic aromatic hydrocarbons, and phenols were 100 %, 100 %, 63.58 %, and 94.12 %, respectively. Research on the physiological response of microbial cells showed that, under optimal ratio regulation, co-metabolic substrates led to a substantial rise in microbial extracellular polymeric substances (EPS) secretion, particularly extracellular proteins. When the system reached the end of its operation, the contents of loosely bound EPS (LB-EPS) and tightly bound EPS (TB-EPS) for proteins in the optimal group were 7.12 mg/g-SS and 152.28 mg/g-SS, respectively. Meanwhile, the ratio of α-Helix / (β-Sheet + Random coil) and the proportion of intermolecular interaction forces were also increased in the optimal group. At system completion, the ratio of α-Helix / (β-Sheet + Random coil) reached 0.717 (LB-EPS) and 0.618 (TB-EPS), respectively. Additionally, the proportion of intermolecular interaction forces reached 74.83 % (LB-EPS) and 55.03 % (TB-EPS). An in-depth analysis of the metabolic regulation of microorganisms indicated that the introduction of optimal ratios of co-metabolic substrates contributed to a noteworthy upregulation in the expression of Catechol 2,3-dioxygenase (C23O) and Dehydrogenase (DHA). The expression levels of C23O and DHA were measured at 0.029 U/mg Pro·g MLSS and 75.25 mg TF·(g MLSS·h)−1 (peak value), respectively. Correspondingly, enrichment of aromatic compound-degrading bacteria, including Thauera, Saccharimonadales, and Candidatus_Competibacter, occurred, along with the upregulation of associated functional genes such as Catechol 1,2-dioxygenase, Catechol 2,3-dioxygenase, Protocatechuate 3,4-dioxygenase, and Protocatechuate 4,5-dioxygenase. Considering the intricate system of multiple coexisting aromatic compounds in real CCW, this study not only obtained an optimal ratio for carbon source addition but also enhanced the efficient utilization of carbon sources and improved the capability of the system to effectively degrade aromatic compounds. Additionally, this paper established a theoretical foundation for metabolic regulation and harmless treatment within the biochemical treatment of intricate systems, exemplified by real CCW.

Ultrathin photonic crystal based on photo-crosslinked polymer and metal–organic framework for highly sensitive detection and discrimination of benzene series vapors

Volatile organic compounds (VOCs) have always been a major concern as a global environmental problem. As a low-cost, high-efficiency and visual sensor, photonic crystals (PCs) have been actively studied in VOCs detection. Herein, a one-dimensional PC sensor for visual sensing of highly toxic benzene series VOC vapors is prepared for the first time by integrating a new photo-crosslinked polymer-poly(styrene-benzoylphenyl acrylate) P(St-BPA) and a high specific surface area metal–organic framework (MOF) MIL-101(Cr). The PC can detect VOCs quantitatively and visually, and clearly distinguish 7 benzene series vapors. The detection limit of the benzene series VOCs is as low as 0.06–3.45 g/m3. Meanwhile, owing to the ultra-thin layer and porous structure, the PC can reach a response equilibrium to the VOCs within 1–2.6 s. Moreover, the PC has a good organic vapor tolerance and can maintain stable optical performance after 1000 times of reuse in VOCs. Besides, 4 other PCs assembled with different aryl polymers and MOFs are first fabricated and their sensing performance to benzene series VOCs are studied and compared, which provides a valuable reference for the selection of materials for the preparation of such PC sensors.

Organic Geochemical Evidence for the Formation of Condensate from Coaly Source Rocks in the Wumaying Buried Hill of the Huanghua Depression, Bohai Bay Basin.

Although oil and gas from coaly source rocks have been widely discovered worldwide, the role of oil generated from coal measures in marine-continental coaly deposits during the Carboniferous-Permian period in the Bohai Bay Basin has long been a subject of debate. The recent discovery of a condensate reservoir in the Wumaying buried hill within the Huanghua Depression of the Bohai Bay Basin offers new potential insights into this issue. In this study, we employed organic geochemical methods to explore the possibility of the Carboniferous-Permian coal deposit being a primary source of the condensate. The distribution of light hydrocarbons and the biomarker assemblage indicate that the condensate did not undergo significant secondary alterations such as thermal cracking, gas invasion fractionation, or biodegradation. The hydrocarbon generation potential of the Carboniferous-Permian coaly source rocks suggests that they could be an important contributor to the formation of condensate. High pristine/phytane ratios (1.0-7.5), an abundant presence of benzene series, and the dominance of C29 steranes (>50%) within the condensate could be indicative of coaly organic matter. These features are comparable to those found in coaly source rocks. Moreover, the stable carbon isotopic compositions of n-alkanes in the condensate, ranging from -26.0 to -30.0‰, correlate well with those from coaly mudstone (-25.4 to -30.0‰). This suggests that the condensate of the Wumaying buried hill may predominantly originate from the Carboniferous-Permian coaly mudstone. When integrated with the geological background, the results distinctly demonstrate that the Carboniferous-Permian coaly source rocks have significantly contributed to the formation of the condensate reservoir in the Wumaying buried hill. This provides an essential reference for future exploration of oil and gas resources derived from the carboniferous-Permian coaly source rocks in the Bohai Bay Basin.

In-situ growth of MIL-101(Fe) onto PET base for high-efficiency adsorption of low concentrations benzene series VOCs and easy recycling

With the proliferation of vehicles in households, people are spending more and more time in their cars, so it is important to ensure the air quality and safety of the car. In this research, environmentally friendly, green PET@PDA@MIL-101(Fe) (PPM) was prepared by in-situ solvothermal growth and acid etching methods, which was categorized by SEM, FTIR, XRD, XPS, and BET. PPM was used to adsorb benzene, toluene, and m-xylene at low concentrations. The maximum amount of adsorption of PET@PDA@MIL-101(Fe) (PPM) for benzene, toluene, and m-xylene was 68.72 mg/g, 91.63 mg/g, and 78.47 mg/g respectively. The adsorption process of PPM is well fitted by the pseudo-first-order kinetic model and Langmuir isothermal adsorption model. Furthermore, PPM exhibited excellent toluene removal performance in simulated vehicles and excellent cycling capability in adsorption-desorption experiments. As a result, PPM can be used to treat and manage toluene volatile organic compounds (VOCs) at low concentrations.

Selective separation characteristics and mechanism of oil substances with different occurrence states in coal chemical wastewater

In response to the complex nature of oil substances in coal chemical wastewater (CCW), and the challenges they pose in separation and removal, this study conducted a detailed analysis of the occurrence, composition, and content of oil substances in CCW. The selective separation characteristics and mechanisms of various materials for oil substances in different occurrence states were explored. The results revealed four main states of oil substances in CCW: suspended oil, dispersed oil, emulsified oil, and dissolved oil, with respective contented of 37.17 %, 27.82 %, 17.79 %, and 17.22 %. These oil substances primarily consisted of alkanes, aromatic hydrocarbons, benzene series, and phenolic compounds, with a total concentration of 2942.18 mg/L. Based on the investigation of the characteristics of oil substances and relevant characterization analyses, the study further explored the selective separation characteristics and mechanisms of different materials for oil substances in various occurrence states. The results indicated that activated carbon, resin, fiber balls, and oil-absorbing felt exhibited excellent selective removal efficiency for dissolved oil, emulsified oil, suspended oil, and dispersed oil, with removal rates of 79.28 %, 63.33 %, 66.89 %, and 55.54 %, respectively. These findings provide theoretical support for the selective separation and recovery of oil substances in CCW, showcasing significant practical applications.

Health damage assessment of commuters and staff in the metro system based on field monitoring-A case study of Nanjing.

The metro has emerged as a major mode of transportation. A significant number of commuters and staff in the metro system are exposed to air pollutants because of its shielded environment, and substantial health damage requires quantitative assessment. Previous studies have focused on comparing the health impacts among different transportation modes, overlooking the specific population characteristics and pollutant distribution in metro systems. To make improvements, this study implements field monitoring of the metro's air environment utilizing specialized instruments and develops a health damage assessment model. The model quantifies health damage of two main groups (commuters and staff) in metro systems at three different areas (station halls, platforms, and metro cabins) due to particulate matter 10 and benzene series pollution. A case study of Nanjing Metro Line 3 was conducted to demonstrate the applicability of the model. Health damage at different metro stations was analyzed, and the health damage of commuters and staff was assessed and compared. This study contributes to enhancing research on health damage in the metro systems by providing a reference for mitigation measures and guiding health subsidy policies.

Adsorbate dissociation due to heteromolecular electronic energy transfer from fluorobenzene thin films.

Study of the near-UV photodissociation dynamics for monolayer (ML) quantities of CH3I on thin films of a series of fluorobenzenes and benzene (1-25 ML) grown on a Cu(100) substrate finds that in addition to gas-phase-like neutral photodissociation, CH3I dissociation can be enhanced via electronic energy transfer to the CH3I following photoabsorption in several of the thin films studied. Distinct CH3 photofragment kinetic energy distributions are found for CH3I photodissociation on C6H5F, 1,4-C6H4F2 and C6H6 thin films, and distinguished from neutral photodissociation pathways using polarized incident light. The effective photodissociation cross section for CH3I on these thin films is increased as compared to that for the higher F-count fluorobenzene thin films due to the additional photodissociation pathway available. Quenching by the metal substrate of the photoexcitation via this new pathway suggests a significantly longer timescale for excitation than that of neutral CH3I photodissociation. The observations support a mechanism in which neutral photoexcitation in the thin film (i.e. an exciton) is transported to the interface with CH3I, and transfers the electronic excitation to the CH3I which then dissociates. The unimodal CH3 photofragment distribution and observed kinetic energies on the fluorobenzene thin films suggest that the dissociation occurs via the 3Q1 excited state of CH3I.