Volatile Organic Compounds Pollution Research Articles

Enhancing Oxygen Activation Ability by Composite Interface Construction over a 2D Co3O4-Based Monolithic Catalyst for Toluene Oxidation.

Developing robust metal-based monolithic catalysts with efficient oxygen activation capacity is crucial for thermal catalytic treatment of volatile organic compound (VOC) pollution. Two-dimensional (2D) metal oxides are alternative thermal catalysts, but their traditional loading strategies on carriers still face challenges in practical applications. Herein, we propose a novel in situ molten salt-loading strategy that synchronously enables the construction of 2D Co3O4 and its growth on Fe foam for the first time to yield a unique monolithic catalyst named Co3O4/Fe-S. Compared to the Co3O4 nanocube-loaded Fe foam, Co3O4/Fe-S exhibits a significantly improved catalytic performance with a temperature reduction of 44 °C at 90% toluene conversion. Aberration-corrected scanning transmission electron microscopy and theoretical calculation suggest that Co3O4/Fe-S possesses abundant 2D Co3O4/Fe3O4 composite interfaces, which promote the construction of active sites (oxygen vacancy and Co3+) to boost oxygen activation and toluene chemisorption, thereby accelerating the transformation of reaction intermediates through Langmuir-Hinshelwood (L-H) and Mars-van Krevelen (MvK) mechanisms. Moreover, the growth mechanism reveals that 2D Co3O4/Fe3O4 composite interfaces are generated in situ in molten salt, inducing the growth of 2D Co3O4 onto the surface lattice of 2D Fe3O4. This study provides new insights into enhancing oxygen activation and opens an unprecedented avenue in preparing efficient monolithic catalysts for VOC oxidation.

Advancements in miniaturized infrared spectroscopic-based volatile organic compound sensors: A systematic review

The global trends of urbanization and industrialization have given rise to critical environmental and air pollution issues that often receive insufficient attention. Among the myriad pollution sources, volatile organic compounds (VOCs) stand out as a primary cluster, posing a significant threat to human society. Addressing VOCs emissions requires an effective mitigation action plan, placing technological development, especially in detection, at the forefront. Photonic sensing technologies rooted in the infrared (IR) light and matter interaction mechanism offer nondestructive, fast-response, sensitive, and selective chemical measurements, making them a promising solution for VOC detection. Recent strides in nanofabrication processes have facilitated the development of miniaturized photonic devices and thus sparked growing interest in the creation of low-cost, highly selective, sensitive, and fast-response IR optical sensors for VOC detection. This review work thus serves a timely need to provide the community a comprehensive understanding of the state of the art in this field and illuminate the path forward in addressing the pressing issue of VOC pollution.

Analysis of Ozone and VOCs Pollution Characteristics, Sources, and Abatement Control Strategies in Hebi

In order to control the increasing ozone （O3） pollution in Hebi, Henan Province, clarifying the pollution characteristics of ozone and its precursors is vital. Therefore, we conducted a comprehensive analysis of O3 pollution utilizing the OFP-PMF-EKMA method combined with online hourly resolution monitoring data of conventional pollutants and volatile organic compounds （VOCs） in the summer of 2022 （June-September）. Ozone formation potential （OFP） was used to identify the key VOCs species, and the PMF model was used to identify the VOCs emission sources, whereas EKMA curves and scenario analysis were used to identify the main ozone control area in Hebi and to determine the reduction ratio of VOCs and NOx in a scientifically refined way. In 2022, Hebi had persistent O3 pollution, with the highest concentration in June. Conditions of high temperature, low humidity, and low atmospheric pressure contributed to the O3 accumulation. Aromatic and oxygenated volatile organic compounds （OVOCs） contributed significantly to the OFP and VOCs fraction, which were the dominant active substance and concentration dominant species. The results of the VOCs source analysis indicated that vehicle exhaust sources （25.3%） were the main source of atmospheric VOCs, followed by process sources （17.7%） and biomass combustion sources （17.6%）. Thus, emission sources associated with the combustion of fossil fuels and industrial production emissions were the most urgent sources of atmospheric VOCs to be controlled in Hebi. The O3 generation in Hebi occurred in the VOCs-sensitive zones, and the emission reduction results showed that a synergistic emission reduction of VOCs and nitrogen oxide （NOx） could effectively control O3 pollution with a 75% reduction in VOCs and a 10% reduction in NOx.

Aqueous VOCs in complex water environment of oil exploitation sites: Spatial distribution, migration flux, and risk assessment

Pollution of the aqueous environment by volatile organic compounds (VOCs) has caused increasing concerns. However, the occurrence and risks of aqueous VOCs in oil exploitation areas remain unclear. Herein, spatial distribution, migration flux, and environmental risks of VOCs in complex surface waters (including River, Estuary, Offshore and Aquaculture areas) were investigated at a typical coastal oil exploitation site. Among these surface waters, River was the most polluted area, and 1,2-Dichloropropane—which emerges from oil extraction activities—was the most prevalent VOC. Positive matrix factorization showed that VOCs pollution sources changed from oil exploitation to offshore disinfection activities along River, Estuary, Offshore and Aquaculture areas. Annual volatilization of VOCs to the atmosphere was predicted to be ∼34.42 tons, and rivers discharge ∼23.70 tons VOCs into the Bohai Sea annually. Ecological risk assessment indicated that Ethylbenzene and Bromochloromethane posed potential ecological risks to the aquatic environment, while olfactory assessment indicated that VOCs in surface waters did not pose an odor exposure risk. This study provides the first assessment of the pollution characteristics of aqueous VOCs in complex aqueous environments of oil exploitation sites, highlighting that oil exploitation activities can have nonnegligible impacts on VOCs pollution profiles.

Application of fluorescent carbon quantum dots functional modified carboxymethyl cellulose film in toluene gas specific detection

With the increasing consumption of organic solvents in chemical and pharmaceutical industries, the environment pollution of volatile organic compounds (VOCs) has become an urgent problem. Therefore, the rapid-visual detection method is of great significance in the analysis of VOCs. Based on the fluorescence quenching/enhancement mechanism of carbon quantum dots (CQDs), with the help of carboxymethyl cellulose membrane with porous and large specific surface area structure, a series of green CQDs@carboxymethyl cellulose composite film (CQDs@CMC composite film) was prepared in this study. In the typical-targeted pollutants (toluene) detection application, a fluorescence spectroscopy method was established which could achieve the high sensitivity and strong specificity detection. The mainly conclusions were as follows: The fluorescence spectrometric detection method for toluene: A kind of hydrophobic Lmi/Bet CQDs@CMC composite film was prepared and characterized with imidazole/betaine CQDs and porous carboxymethyl cellulose composite film as raw materials. The toluene detection performance was studied, and the recognition mechanism was explored. The results showed that toluene enhanced the fluorescence of Lmi/Bet CQDs@CMC composite film. The fluorescence intensity of composite films was proportional to toluene concentration when the toluene concentration ranged from 200 to 2200 mg/L. The detection limit of toluene was 1.169 mg/L, which provides a theoretical basis for the detection of toluene by fluorescence spectrometry.

Hierarchical porous carbon nanofibrous membranes with elaborated chemical surfaces for efficient adsorptive removal of volatile organic compounds from air

Volatile organic compounds (VOCs) in the air pose great health risks to humans and the environment. Adsorptive separation technology has proven effective in mitigating VOC pollution, with the adsorbent being the critical component. Therefore, the development of highly efficient adsorbent materials is crucial. Carbon nanofibers, known for their physical–chemical stability and rapid adsorption kinetics, are promising candidates for removing VOCs from the air. However, the relatively simple porous structures and inert surface chemical properties of traditional carbon nanofibers present challenges in further enhancing their application performance further. Herein, a hierarchical porous carbon nanofibrous membrane was prepared using electrospinning technology and a one-step carbonization & activation method. Phenolic resin and polyacrylonitrile were used as co-precursors, with silica nanoparticles serving as the dopant. The resulting membrane exhibited a specific surface area of up to 1560.83 m2/g and surfaces rich in functional O-/N- groups. With a synergistic effect of developed micro- and meso-pores and active chemical surfaces, the carbon nanofibrous membrane demonstrated excellent adsorption separation performance for various VOCs, with comparable adsorption capacities and fast kinetics. Moreover, the membrane displayed remarkable reusability and dynamic adsorption performance for different VOCs, indicating its potential for practical applications.

A well-engineered two-dimensional coral-like architecture CNWO3 for the effective removal of volatile organic compounds from indoor air

One of the promising strategies to enhance the photocatalytic performance of graphitic carbon nitride (CN) is to establish 2D photocatalysts with boosted morphology and adjusted charge transfer direction. Herein, a green and sustainable strategy (water used as solvent) is employed to fabricate a coral-like CNWO3 with highly desirable visible-light photocatalytic activity. The coral-like structure provides more atoms at the edges and corners to act as active antennae to enhance the photocatalytic activity. These new antennae generate various active sites that are short enough to drive strong visible light harvesting, while being large enough to prevent intense quantum confinement effects. Under visible-light irradiation (λ > 400 nm), the as-prepared photocatalyst effectively removes gaseous acetaldehyde (90.5 %) and toluene (73.4 %), the two most common volatile organic compounds (VOCs) in indoor air, possibly due to its unique structure. The DFT calculations clearly show that the interaction of acetaldehyde and toluene over CNWO3 is energetically more favorable than that over CN. Both the hydroxyl (OH) and superoxide (O2−) that are generated by the photocatalyst play a substantial role in VOCs degradation. This work highlights the solar-active photocatalysis development using a synergy of morphology and material nature for sophisticated gas-phase reactions to effectively solve VOCs pollution issues of the indoor environment.

Stereoscopic imaging of volatile organic compounds distribution in the region and tracing emission sources of volatile organic compounds using a novel movable single-photon ionization time-of-flight mass spectrometer.

This paper presents a newly developed high-performance mobile single-photon ionization time-of-flight mass spectrometry (M-SPI-TOFMS) system for on-line analysis and stereoscopic monitoring of complex gas mixtures. The system is designed for stereoscopic imaging to map the distribution of volatile organic compounds (VOCs) and trace their emission sources in urban areas and industrial parks. It mainly consists of a SPI-TOFMS instrument, a customized commercial vehicle, a meteorological five-parameter monitor with GPS, a high-power generator, and an uninterruptible power supply. The SPI technique, using a 118 nm VUV lamp, can ionize compounds with an ionization potential below 10.78 eV. Mass spectra obtained using this technique show the profiles of various VOCs and some inorganic compounds. The VOCs composition information and mobile location data are simultaneously sent to the GIS software. In GIS software, this data is used for real-time stereoscopic imaging of VOC distribution and precise tracking of VOC movement. The system can achieve a spatial data resolution of 0.69 mm at 25 km/h due to the microsecond detection speed of the M-SPI-TOFMS instrument. The laboratory test provides a rapid overview characterization of benzene, toluene, and xylene. The M-SPI-TOFMS has limits of detection and mass resolution of 33.7 pptv and 1060, respectively. Several field applications were carried out using M-SPI-TOFMS at various locations to identify VOC sources near different factories. The M-SPI-TOFMS system has a navigation monitoring speed of 25 km/h with a time resolution of 1 s. The widespread use of this system will provide accurate data to support environmental management departments in formulating VOCs pollution control policies and improving control efficiency.

Exogenous of different elicitors: proline and ornithine on Sansevieria trifasciata under particulate matter (PM) and volatile organic compounds (VOC).

Phytoremediation has become famous for removing particulate matter (PM) and volatile organic compounds (VOC) in situ. Plants for removing PM and VOC were associated with botanical biofilters to attract pollution to the plant. On the other hand, persistent pollution exposure can lower plant health and phytoremediation effectiveness; therefore, improving plant tolerance against stress is necessary. Various elicitors can enhance plant tolerance to certain stressors. This study aims to investigate different elicitors to maintain plant health and improve the use of plants in phytoremediation for PM and VOC pollution. This experiment used Sansevieria trifasciata hort. ex Prain under PM and VOC stress. Exogenous elicitors, such as proline, ornithine, and a commercial product, were applied to the leaf parts before exposure to PM and VOC stress. The initial concentrations of PM1, PM2.5, and PM10 were 300-350, 350-450, and 400-500µgm-3, respectively, while the VOC concentration was 2.5-3.0mgm-3. The plant was stressed for 7days. The result indicated that ornithine 10mM is vital in improving plant tolerance and inducing antioxidant enzymes against PM and VOC, while proline 50mM and a commercial product could not reduce plant stress. This study suggests that ornithine might be an important metabolite to improve plant tolerance to PM and VOC.

Absorption performance and mechanism of volatile organic compounds by phosphonium ionic liquids with different anions

AbstractBACKGROUNDThe emission of volatile organic compounds (VOCs) seriously harms the environment and human health. The prevention and control of VOCs pollution is a major challenge in the research field. Aiming at VOCs pollution treatment using green solvents, the absorptions of trichloromethane by synthesized tributyl(propyl)phosphonium bis(trifluoromethylsulfonyl)imide ([P4443][Tf2N]), tributyl(propyl)phosphonium tetrafluoroborate ([P4443][BF4]), tributyl(propyl)phosphonium trifluoroacetic acid ([P4443][CF3COO]) and xylene by trioctyl(propyl)phosphonium bis(trifluoromethylsulfonyl)imide ([P8883][Tf2N]) and trioctyl(propyl)phosphonium tetrafluoroborate ([P8883][BF4]) were experimentally measured. The mechanism of trichloromethane and xylene being absorbed by PILs with different anions was further discussed through simulation calculation.RESULTSThe phosphonium‐based ionic liquids (PILs) process excellent absorption capacity, such as [P4443][CF3COO] with the static saturation absorbing capacity up to 2.843 g/g for trichloromethane. PILs have a certain selective absorption ability for xylene, which has the highest absorption for o‐xylene reaching 1.462 g/g. The absorption energy data also prove that [CF3COO]− anion preferentially interacts with trichloromethane. Combine with the most stable structures of VOCs absorbed by PILs, the results of the Mulliken charge and frontier molecular orbitals indicate that PILs anions play a major role in chlorinated alkanes, and form hydrogen bonds with them. In addition, the cation can form C‐H…π bond interaction with xylene.CONCLUSIONThe experimental and calculated results showed that PILs is a promising adsorbent for trichloromethane and xylene. It provides reference for PILs designed to deal with VOCs in the future.This article is protected by copyright. All rights reserved.

Novel approach for identifying VOC emission characteristics based on mobile monitoring platform data and deep learning: Application of source apportionment in a chemical industrial park

Refined volatile organic compound (VOC) emission characteristics are crucial for accurate source apportionment in chemical industrial parks. The data from mobile monitoring platforms in chemical industrial parks contain pollution information that is not intuitively displayed, requiring further excavation. A novel approach was proposed to identify VOC emission characteristics using the class activation map (CAM) technology of convolutional neural network (CNN), which was applied on the mobile monitoring platform data (MD) derived from a typical fine chemical industrial park. It converts a large amount of monitoring data with high spatiotemporal complexity into simple and interpretable characteristic maps, effectively improving the identification effect of VOC emission characteristics, supporting more accurate source apportionment of VOC pollution around the park. Using this method, the VOC emission characteristics of eight key factories were identified. VOC source apportionment in the park was conducted for one day using a positive matrix factorization (PMF) model and seven combined factor profiles (CFPs) were calculated. Based on the identified VOC emission characteristics, the main pollution sources and their contributions to surrounding schools and residential areas were determined, revealing that one pesticide factory (named LKA) had the highest contribution ratio. The source apportionment results indicated that the impact of the chemical industrial park on the surrounding areas varied from morning to afternoon, which to some extent reflected the intermittent production methods employed for fine chemicals.

Environmental radon, fracking wells, and lymphoma in dogs.

Multicentric lymphoma (ML) in dogs resembles non-Hodgkin lymphoma (NHL) in humans. Human NHL is associated with multiple environmental exposures, including to radon and volatile organic compounds (VOCs). The objective of this study was to determine whether ML in dogs was associated with environmental radon or proximity to horizontal oil and drilling (fracking), a source of VOC pollution. We identified dogs from the Golden Retriever Lifetime Study that developed ML (n = 52) along with matched controls (n = 104). Dog home addresses were categorized by Environmental Protection Agency radon zone and average residential radon by county, as well as by distance from fracking and associated wastewater wells. We found no significant differences in county level radon measurements. Individual household radon measurements were not available. There was no difference in residential proximity to active fracking wells between dogs with ML and unaffected dogs. While dogs with ML lived closer to wastewater wells (123 vs 206 km; P = .01), there was no difference in the percentage of cases vs controls that lived in close proximity (20 km) to a fracking well (11.5% for cases, 6.7% for controls; OR 1.81, 95% CI 0.55 to 5.22; P = .36), or a wastewater well (6.7% for cases, 4.4% for controls; P > .99). These data suggest that more proximate sources of chemical exposures need to be assessed in dogs with ML, including measurements of individual household radon and household VOC concentrations.

High-solution emission characters and health risks of volatile organic compounds for sprayers in automobile repair industries.

The increasing automobile repair industries (ARIs) with spray facilities have become an important volatile organic compound (VOC) pollution source in China. However, the VOC health risk assessment for long-term exposure in ARIs has not been well characterized. In this study, though sampled VOCs from 51 typical ARIs in Beijing, the relationship between emission patterns, average daily exposure concentrations (EC), and health risks was comprehensively analyzed with the health assessment method. Results showed that concentrations of 117 VOCs from the samples ranged from 68.53 to 19863.32 μg·m-3, while the ARI operator's daily VOC inhalation EC was 11.24-1460.70 μg·m-3. The organic VOC (OVOC) concentration accounted for 73.16 ~ 94.52% in the solvent-based paint workshops, while aromatics were the main VOC component in water-based paint spraying (WPS) workshops, accounting for 70.08%, respectively. And the method of inhalation exposure health risk assessment was firstly used to evaluate carcinogenicity and non-carcinogenicity risk for sprayers in ARIs. The cumulative lifetime carcinogenic risk (LCR) for 24 sampled VOCs were within acceptable ranges, while the mean hazard index (HI) for 1 year with 44 sampled VOCs was over 1. Among them, ethyl alcohol had a high carcinogenic risk in both mixed water-based paint (MP) and solvent-based paint workshops. The mean HI associated with aromatics were 2.88E - 3 and 4.30E - 3 for 1 h in MP and WPS workshops. O-ethyl toluene and acetone are VOC components that need to be paid attention to in future paint raw materials and spraying operations. Our study will provide the important references for the standard of VOC occupational exposure health limits in ARIs.

Quantitative analysis on chemical influence of modified activated carbon in TSA/PSA for methanol via alterable phosphorus functional groups and stable structure

Volatile organic compounds (VOCs) emissions cause serious health problems and environmental pollution, and modified activated carbon is widely used in the treatment of VOCs pollution. Methanol was selected as adsorbate and activated carbon with alterable phosphorus functional groups was synthesized as adsorbent. In the absence of the influence of the physical properties, the chemical functional groups influence coefficient (AC) was proposed, which can be used to analysis and predict the influence of chemical functional groups specially. The results show that the performances including adsorption capacity and enrichment ratio are positively related to the AC whether in temperature swing adsorption (TSA) or pressure swing adsorption (PSA). By comparison, the adsorption capacity of PSA is greater than that of TSA because of the higher efficiency caused by faster cycle. Further research on process showed that the curve character of TSA, including breakthrough time and equilibrium time, is highly related with AC, but the curve character of PSA is mainly depended on the state of activated carbon. Therefore, the attenuation of TSA is mainly caused by the change of chemical functional groups, while the attenuation of PSA is mainly caused by the failure of activated carbon.

A prediction index of the volatile organic compounds pollution conditions in a chemical industrial park based on atmospheric stability

Volatile organic compounds (VOCs), as common precursors of ozone (O3) and fine particulate matter (PM2.5), are a focus of air pollution prevention and control. Furthermore, with the rapid development of industry, industrial sources have become the largest source of anthropogenic VOCs emissions, leading to economic development while causing great harm to the environment. It is becoming meaningful to efficiently predict the future total volatile organic compounds (TVOC) pollution conditions in chemical industrial parks (CIPs), which can assist managers in carrying out corporate emission management in advance. In this study, TVOC monitoring data and meteorological data from January 1, 2022, to December 31, 2022, were used to innovatively construct the TVOC pollution index. This index comprehensively considers the atmospheric stability and localized horizontal diffusion conditions and can quickly and accurately predict the variations in the TVOC in a CIP in the next 7 days. In addition, we used synoptic weather patterns and backward trajectory analysis to explore the mechanism of VOCs pollution formation in a CIP. The results show that the combined influences of a westerly wind pattern, temperatures above 30 °C, a subtropical high pressure system, more upwind pollutants, and the horizontal and vertical diffusion conditions in the CIP were unfavorable, leading to VOCs pollution.

Performance enhancement analysis of a liquid desiccant dehumidifier with internal cooling for indoor benzene removal

Indoor volatile organic compounds (VOCs) pollution is becoming increasingly serious, posing a huge threat to human health. The removal of VOCs has always been a challenge in air purification processes. In this regard, conventional VOC removal methods are often not ideal. Liquid desiccant (LD) dehumidification is a new removal method proposed recently and becoming increasingly used in many applications. Previous studies dealing with LD mainly focused on adiabatic dehumidifiers, but the results are not very promising. The main reason for this is the significant temperature rise of the LD solution, which seriously affects the mass transfer of the VOC. To enhance mass transfer performance, it is important to suppress temperature rise. In this study, internal cooling (IC) technology is introduced to enhance benzene mass transfer. A mathematical model is established for modeling and assessing the mass transfer process. The benzene transfer characteristics are studied and compared, considering dehumidifiers with and without IC. The effects of the cooling water, air, LD solution, and transfer parameters on the benzene mass transfer performance are evaluated and identified. Additionally, the distribution differences of the key parameters along the dehumidifier are revealed. The results indicated that benzene transfer performance can be significantly enhanced by adopting IC, with a performance improvement of 28.42%. This improvement is attributed to the decrease in the LD solution temperature caused by IC and the corresponding Henry’s constant. The cooling water parameters, airflow rate, LD solution status, and NTUbenzene are the key factors affecting the removal performance. Overall, employing IC can effectively improve the transfer driving force for benzene, resulting in better benzene transfer performance. This study demonstrates the feasibility and promising potential of using IC technology to enhance benzene transfer in LD dehumidifiers.

Conversion of waste cork to N-doped porous carbons by urea-assisted hydrothermal method for enhanced VOC capture

Converting waste resources into porous carbon for pollutants capture is an effective strategy to achieve the environmental goal of “treating waste with waste”. Cork is an ideal precursor of porous carbons due to its ordered honeycomb-like cell structure and layered composition distribution. Herein, N-doped porous carbons (PCs) were prepared via two steps of urea-assisted hydrothermal carbonization and chemical activation to mitigate volatile organic compounds (VOCs) pollution. Results indicated that the obtained PC4-800 exhibited remarkable features for adsorption including high total pore volume (0.97 cm3/g) and specific surface area (1864.89 m2/g), as well as abundant N-containing functional groups. The excellent pore structure was primarily owing to the corrosion of the carbon matrix by the gas produced from the reaction of K2CO3 and N-containing functional groups. The adsorption results showed that the PC4-800 have an outstanding toluene adsorption capacity (867.03 mg/g) that outperforming majority of adsorbents previously reported. There are substantial pores in N-doped PCs with a pore width of 1.71–2.28 nm, which is 3 to 4 times the molecular dynamic diameter of toluene, and plays a crucial role in the absorption process. Moreover, the promotional influence of N-functional groups on the toluene adsorption process was verified through DFT calculation by Gaussian imitating, where N-6 generated π-electron enrichment sites on the surface of N-doped PCs, facilitating π-π dispersion with the benzene ring in toluene. This study provides a new strategy to convert waste cork into high-performance adsorbents for VOCs removal.

Bimetallic MOF derived mesoporous structure of Ru doped SnO2 enable high-sensitivity gas sensors for triethylamine in high humidity

Mesoporous metal oxides have been reported as promising semiconductor gas sensing materials, showing great potential in detecting volatile organic compound (VOC) pollutants in the air. Here, we present the use of mesoporous Ru doped SnO2 oxide semiconductor, derived from a bimetallic organic framework (MOF), as a composite material for high-performance TEA gas sensing. Mesoporous structure of bimetallic MOF-derived composites synthesised using a one-step method, has a high porosity and large specific surface area (69.48 m2 g−1), which can enhance the number of sensing reaction sites and improve its capturing ability for the target gas. Moreover, the in-situ substitution of Ru3+ ions for Sn4+ ions can adjust the carrier concentration. Therefore, the synthesized mesoporous 0.4 mol% Ru-SnMOF@SnO2 exhibits high sensitivity, excellent selectivity, fast response kinetics, and good long-term stability for TEA sensing at 250 °C. Exceptionally, there is still an impressive response (S = 125.5–100 ppm) to triethylamine at 80 % RH. The relative humidity was set at 25 °C.

Thermocatalytic oxidation of a binary mixture of formaldehyde and toluene at ambient levels by a titanium dioxide supported platinum catalyst

The thermocatalytic oxidative potential of various supported noble metal catalysts (SNMCs) is well-known for hazardous volatile organic compounds (VOCs), e.g., formaldehyde (FA) and toluene. However, little is known about SNMC performance against ambient VOC pollution with low concentration (subppm levels) relative to industrial effuluents with high concentrations (several hundred ppm). Here, the thermocatalytic oxidation performance of a titanium dioxide (TiO2)-supported platinum catalyst (Pt/TiO2) has been evaluated for a low-concentration binary mixture of FA and toluene at low temperatures and in the dark. A sample of TiO2 containing 1 wt% Pt with thermal reduction pre-treatment under hydrogen achieved 100 % conversion of FA (500 ppb) and toluene (100 ppb) at 130 °C and a gas hourly velocity of 59,701 h−1. Its catalytic activity was lowered by either a decrease in catalyst mass or an increase in VOC concentration, relative humidity, or flow rate. In situ diffuse reflectance infrared Fourier transform spectroscopy, density functional theory simulations, and molecular oxygen (O2) temperature–programmed desorption experiments were used to identify possible VOC oxidation pathways, reaction mechanisms, and associated surface phenomena. The present work is expected to offer insights into the utility of metal oxide-supported Pt catalysts for the low-temperature oxidative removal of gaseous VOCs in the dark, primarily for indoor air quality management.

Pollution characteristics and secondary formation potential of volatile organic compounds in the multi-industrial city of Ulsan, Korea

The secondary formation of ozone and aerosols due to volatile organic compounds (VOCs) has drawn increased attention in Ulsan, a multi-industrial city in South Korea. In this study, 52 VOCs were measured at 40 sites in four industrial (petrochemical, nonferrous, automobile, and shipbuilding) complexes and five urban sites using passive air samplers. The concentration of aromatics (44.6 μg/m3) accounted for 70.3% of the total VOC concentration (63.4 μg/m3), which was significantly higher than those of alkanes (27.5% and 17.4 μg/m3) and alkenes (2.15% and 1.37 μg/m3). The highest concentrations of total VOCs and aromatics were observed at the shipbuilding industrial complex, whereas the concentration of alkanes and alkenes was the highest in the petrochemical industrial complex. The positive matrix factorization (PMF) model suggested five major VOC sources in urban areas: (1) petrochemical production processes, (2) fuel combustion and evaporation, (3) urban emissions sources, (4) solvent use, and (5) painting and metal surface coating. The PMF result indicated that the distances from the four industrial complexes substantially affected VOC pollution in the urban areas. Moreover, aromatics (e.g., m,p-xylenes, toluene, ethylbenzene, o-xylene, and 1,2,4-trimethylbenzene) exhibited higher ozone formation potential (OFP) and secondary organic aerosol formation potential (SOAFP), which were mainly emitted from solvent use and painting in the shipbuilding and automobile industrial complexes. The petrochemical industrial complex close to densely populated urban areas also contributed significantly to secondary formation potential. In conclusion, our study revealed that elevated levels of aromatics were associated with increased OFP and SOAFP. Additionally, the four industrial complexes exhibited varying impacts on pollution characteristics in urban areas. These findings have practical implications, as they can inform the development of industry-specific management strategies for mitigating VOC pollution and secondary formation in multi-industrial cities.