Toxic Volatile Organic Compounds Research Articles

Volatile organic compounds in the atmosphere of Mexico City

The Mexico City Metropolitan Area (MCMA) is one of the most polluted megacities in North America. Therefore, it is an excellent benchmark city to understand atmospheric chemistry and to implement pilot countermeasures. Air quality in the MCMA is not within acceptable levels, mainly due to high ground levels of ozone (O3). Tropospheric O3 is a secondary pollutant formed from the oxidation of volatile organic compounds (VOCs) in the presence of nitrogen oxides and sunlight. To gain a better understanding of O3 formation in megacities, evaluate the effectiveness of already-implemented countermeasures, and identify new cost-effective alternatives to reduce tropospheric O3 concentrations, researchers and environmental authorities require updated concentrations for a broader range of VOCs. Moreover, in an effort to protect human health and the environment, it is important to understand which VOCs exceed reference safe values or most contribute to O3 formation, as well as to identify the most probable emission sources of those VOCs. In this work, 64 VOCs, including 36 toxic VOCs, were measured at four sites in the MCMA during 2011–2012. VOCs related to liquefied petroleum gas leakages exhibited the highest concentrations. Toxic VOCs with the highest average concentrations were acetone and ethanol. The toxic VOC benzene represented the highest risk to Mexican citizens, and toluene contributed the most to O3 formation. Correlation analysis indicated that the measured VOCs come from vehicular emissions and solvent-related industrial sources.

Occurrence and Concentrations of Toxic VOCs in the Ambient Air of Gumi, an Electronics-Industrial City in Korea.

This study was carried out to characterize the occurrence and concentrations of a variety of volatile organic compounds (VOCs) including aliphatic, aromatic, halogenated, nitrogenous, and carbonyl compounds, in the ambient air of Gumi City, where a large number of electronics industries are found. Two field monitoring campaigns were conducted for a one year period in 2003/2004 and 2010/2011 at several sampling sites in the city, representing industrial, residential and commercial areas. More than 80 individual compounds were determined in this study, and important compounds were then identified according to their abundance, ubiquity and toxicity. The monitoring data revealed toluene, trichloroethylene and acetaldehyde to be the most significant air toxics in the city, and their major sources were mainly industrial activities. On the other hand, there was no clear evidence of an industrial impact on the concentrations of benzene and formaldehyde in the ambient air of the city. Overall, seasonal variations were not as distinct as locational variations in the VOCs concentrations, whereas the within-day variations showed a typical pattern of urban air pollution, i.e., increase in the morning, decrease in the afternoon, and an increase again in the evening. Considerable decreases in the concentrations of VOCs from 2003 to 2011 were observed. The reductions in the ambient concentrations were confirmed further by the Korean PRTR data in industrial emissions within the city. Significant decreases in the concentrations of benzene and acetaldehyde were also noted, whereas formaldehyde appeared to be almost constant between the both campaigns. The decreased trends in the ambient levels were attributed not only to the stricter regulations for VOCs in Korea, but also to the voluntary agreement of major companies to reduce the use of organic solvents. In addition, a site planning project for an eco-friendly industrial complex is believed to play a contributory role in improving the air quality of the city.

Rethinking how volatiles are released from plant cells.

For plant volatile organic compounds (VOCs) to be emitted, they must cross membrane(s), the aqueous cell wall, and sometimes the cuticle, before moving into the gas phase. It is presumed that VOC movement through each barrier occurs via passive diffusion. However, VOCs, which are primarily nonpolar compounds, will preferentially partition into membranes, making diffusion into aqueous compartments slow. Using Fick's first law, we calculated that to achieve observed VOC emission rates by diffusion alone would necessitate toxic VOC levels in membranes. Here, we propose that biological mechanisms, such as those involved in trafficking other hydrophobic compounds, must contribute to VOC emission. Such parallel biological pathways would lower barrier resistances and, thus, steady-state emission rates could be maintained with significantly reduced intramembrane VOC concentrations.

Health risk assessment of toxic VOCs species for the coal fire well drillers.

In this study, the health risk of toxic volatile organic compounds (VOCs) species for well drillers, working at an exposure site around a well of underground coal fire site, was presented in a case of Shanxi province. The samples were collected by Teflon sampling bags and measured by gas chromatography-mass spectrometry (GC-MS). The results showed that isopropyl alcohol was the most abundant compound of VOCs, with the geometric mean concentrations of 1700.38 μg/m(3). The geometric mean concentrations of individual BTEX compounds obtained in all of the sampling campaign were 131.64, 10.15, 15.53, and 25.38 μg/m(3) for benzene, toluene, ethyl-benzene, and xylenes, respectively. Relative proportion of BTEX averaged as 8.5:0.7:1:1.6. High B/T ratio (13.0) and low T/E ratio (0.7) was observed in this study. For non-cancer risk in this study, the hazardous quotient (HQ) of 1,2-dibromoethane, 1,3-butadiene, and benzene was 17.91, 1.71, and 43.88, respectively, mean their non-cancer risk was at the level of definite concern. The HQ sum of 20 VOCs was 64.94, much higher than 1. The cancer risk values of benzene (7.01E-04), 1,2-dibromoethane (1.91E-04), carbon tetrachloride (1.55E-04), and 1,3-butadiene (1.09E-04) were greater than 10(-4), indicating that they were all definite risk. The total cancer risk of all VOCs species was 1.39E-03, almost 14 times more than the level of definite risk. The stochastic exposure assessment of all VOCs species total cancer risk using the Monte Carlo simulation analysis shows that 5 and 95 % cancer risks were predicted to be 7.60E-04 and 2.75E-03, respectively. The cancer risk for all VOCs species is unacceptable. The results of sensitivity analysis show that benzene, carbon tetrachloride, and 1,3-butadiene exposure account for more than 98 % contributions to the estimated risk for drillers, indicating that those VOCs species exposure has greater impact than other species on risk assessment. Both combined effects and independent effects of each VOCs species have to be considered.

Use of Soft Plasma Ionization Source at Evacuated Air Atmospheres in Time-of-Flight Mass Spectrometry to Suppress Fragmentation of Volatile Organic Compounds

ABSTRACT This study describes a measuring system for mass spectrometry, consisting of a glow discharge ionization source for soft plasma ionization and a time-of-flight mass spectrometer, to detect toxic volatile organic compounds rapidly and easily. It is the most important to determine how the complicated fragmentation of such compounds can be suppressed to occur so as to recognize the mass spectra of the volatile organic compounds as their fingerprints. The novelty of this work is that the optimal discharge condition for the soft plasma ionization–time-of-flight mass spectrometer system could be selected, so that the parent mass peak of analyte molecules could be observed both with high sensitivity and with little or no fragmentation of them. Use of air gas at a pressure of 1000 Pa provided the most favorable result for these criteria, whereas, in a previous report, the soft plasma ionization source operating with argon at a pressure of 346 Pa had yielded additional mass peaks of the fragmented species. The reason for this would be explained by the fact that energetic electrons in the plasma, which principally cause the fragmentation of the volatile organic compounds, have lower number density at higher gas pressures, through de-accelerated collisions with the plasma gas.

Preparation of porous SnO2 microcubes and their enhanced gas-sensing property

Porous SnO2 microcubes were obtained through a facile chemical solution route with subsequent calcination and acid-washing process. Their structures and morphology evolution were comprehensively characterized via X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, thermogravimetric–differential thermal analysis, and Brunauer–Emmett–Teller N2 adsorption–desorption analyses. The process of inducing porosity starts with a crystalline single-phase MnSn(OH)6 precursor formed by the co-precipitation of the metal ions from the aqueous solution. Thermal decomposition of the precursors leads to an intimate mixture of Mn3O4 and porous tetragonal SnO2. The SnO2 microcubes are obtained after a hydrothermal acid-washing process. A decomposition–aggregation–dissolution process is proposed to demonstrate the formation of such special structure. Furthermore, the gas-sensing properties of the as-prepared porous SnO2 microcubes were investigated in toxic volatile organic compounds, such as formaldehyde, ethanol, benzene, methanol, acetone, and toluene. The enhanced sensing performance of porous SnO2 microcubes was demonstrated. The detection limits of formaldehyde and ethanol were approximately 0.09 and 0.12ppm (signal-to-noise ratio, S/N=3), respectively, which substantially benefitted from their unique porous structure and large surface area.

Preparation of hollow porous SnO2 microcubes and their gas-sensing property

Hollow porous SnO2 microcubes were obtained through a facile chemical solution route with subsequent calcination and acid-washing process. The process of inducing porosity starts with a crystalline single-phase MnSn(OH)6 precursor formed by the co-precipitation of the metal ions from the aqueous solution. Thermal decomposition of the precursors leads to an intimate mixture of Mn3O4 and porous tetragonal SnO2. The hollow porous SnO2 microcubes are obtained after a simple acid-washing process. Furthermore, the gas-sensing properties of the hollow porous SnO2 microcubes were investigated in toxic volatile organic compounds, such as formaldehyde, toluene, benzene, methanol, acetone, and ethanol. The detection limits of formaldehyde and toluene were approximately 0.08 and 0.19ppm, respectively, which substantially benefitted from their hollow porous structure and large surface area.

Proton Transfer Reaction Time-of-Flight Mass Spectrometric (PTR-TOF-MS) determination of volatile organic compounds (VOCs) emitted from a biomass fire developed under stable nocturnal conditions

Combustion of solid and liquid fuels is the largest source of potentially toxic volatile organic compounds (VOCs), which can strongly affect health and the physical and chemical properties of the atmosphere. Among combustion processes, biomass burning is one of the largest at global scale. We used a Proton Transfer Reaction “Time-of-Flight” Mass Spectrometer (PTR-TOF-MS), which couples high sensitivity with high mass resolution, for real-time detection of multiple VOCs emitted by burned hay and straw in a barn located near our measuring station. We detected 132 different organic ions directly attributable to VOCs emitted from the fire. Methanol, acetaldehyde, acetone, methyl vinyl ether (MVE), acetic acid and glycolaldehyde dominated the VOC mixture composition. The time-course of the 25 most abundant VOCs, representing ∼85% of the whole mixture of VOCs, was associated with that of carbon monoxide (CO), carbon dioxide (CO2) and methane (CH4) emissions. The strong linear relationship between the concentrations of pyrogenic VOC and of a reference species (i.e. CO) allowed us to compile a list of emission ratios (ERs) and emission factors (EFs), but values of ER (and EF) were overestimated due to the limited mixing of the gases under the stable (non-turbulent) nocturnal conditions. In addition to the 25 most abundant VOCs, chemical formula and concentrations of the residual, less abundant VOCs in the emitted mixture were also estimated by PTR-TOF-MS. Furthermore, the evolution of the complex combustion process was described on the basis of the diverse types of pyrogenic gases recorded.

Adsorption equilibrium studies for O‐xylene vapour and modified clays system

Tunisian bentonites were used to prepare three modified clays: two organoclays by intercalating respectively didodecyldimethylammoniumbromide (DDMAC) and hexadecyltrimethylammoniumbromide (HDTMAC), and synthesis of NaX zeolite. The X‐ray diffraction, infrared and thermogravimetric analyses enabled us to differentiate between the structures obtained. Clay materials systems were used as adsorbent for the investigation of the adsorption isotherms and saturation capacity of O‐xylene, a toxic volatile organic compound, by gravimetric method at three different temperatures 20, 30, and 40 °C. The absolute values of the volatile organic compound adsorbed amounts in the intercalated clays (604 mg g−1) were higher than for the zeolite (296 mg g−1). The adsorption isotherms were analysed by the Freundlich and Langmuir equations. The latter was found to describe better the equilibrium adsorption data. Mass transfer coefficient of O‐xylene is evaluated using uptake curve method, and all values are in the order of 10−2 s−1. Copyright © 2014 John Wiley & Sons, Ltd.

Exposure to volatile organic compounds: Comparison among different transportation modes

The increasing trend of promoting public transportation (bus tram, metro, train) and more environmental friendly and sustainable non fossil-fuel alternatives (walking, cycling etc) as substitutes for auto vehicles brings forward new questions with regard to pollutant levels to which commuters are exposed. In this study, three transportation modes (tram, auto vehicle and bicycle) are studied and concentration levels of 84 volatile organic compounds (VOCs) (hydrocarbons, aromatic hydrocarbons, oxygen containing hydrocarbons, terpenes and halogenated compounds) are measured along a route in the city of Ghent, Belgium. The concentration levels are obtained by active sampling on Tenax TA sorbent tubes followed by thermal desorption gas chromatography mass spectrometry (TD-GC-MS) using deuterated toluene as an internal standard. The median total VOC concentrations for the tram mode (33 μg/m³) is 1.7 times higher than that of the bicycle mode (20 μg/m³) and 1.5 times higher than for the car mode (22 μg/m³). It is found that aromatic hydrocarbons account for a significant proportion in the total VOCs concentration (TVOCs) being as high as 41–57%, 59–72% and 58–72% for the tram, car and bicycle respectively. In all transportation modes, there was a high (r > 0.6) degree of correlation between BTEX compounds, isopropylbenzene, n-propylbenzene, 1,3,5-trimethylbenzene and 1,2,4-trimethylbenzene. When comparing time weighed average concentrations along a fixed route in Ghent, it is found that commuters using the tram mode experience the highest TVOCs concentration levels. However, next to the concentration level to which commuters are exposed, the physical activity level involving the mode of transportation is important to assess the exposure to toxic VOCs. It is proven that the commuter using a bicycle (4.3 ± 1.5 μg) inhales seven and nine times more benzene compared to the commuter using the car and tram respectively, when the same route is followed.

Quantification of volatile organic compounds in smoke from prescribed burning and comparison with occupational exposure limits

Abstract. Prescribed burning represents a serious threat to personnel fighting fires due to smoke inhalation. The aim of this study was to investigate exposure by foresters to smoke from prescribed burning, focusing on exposure to volatile organic compounds (VOCs). The methodology for smoke sampling was first evaluated. Potentially dangerous compounds were identified among the VOCs emitted by smoke fires at four prescribed burning plots located around Corsica. The measured mass concentrations for several toxic VOCs were generally higher than those measured in previous studies due to the experimental framework (short sampling distance between the foresters and the flame, low combustion, wet vegetation). In particular, benzene, phenol and furfural exceeded the legal short-term exposure limits published in Europe and/or the United States. Other VOCs such as toluene, ethybenzene or styrene remained below the exposure limits. In conclusion, clear and necessary recommendations were made for protection of personnel involved in fighting fires.

Nematicidal activity of volatile organic compounds emitted by Brassica juncea, Azadirachta indica, Canavalia ensiformis, Mucuna pruriens and Cajanus cajan against Meloidogyne incognita

Understanding the effect of plant volatile organic compounds (VOCs) on soil nematodes and water may explain plant damage in the field and how some nematode management strategies reduce soil nematode populations. M. incognita is a damaging plant pathogenic nematode that affects crops worldwide. The aims of this study were to evaluate the effect of the VOCs emitted by five common crops used for soil incorporation to control the second-stage juveniles (J2) of Meloidogyne incognita. To investigate the “in vitro” role of water in the relationship between nematodes and plant VOCs. And to identify the volatile molecules by gas chromatography (GC/MS). The method used permitted the volatile molecules from macerated plant organs to only contact the J2 nematodes by air. Plants organs from all plants macerated with and without water emitted VOCs that immobilized J2 nematodes, with higher levels emitted when the plant organs were macerated without water. Only water exposed to VOCs from neem and mustard leaves were capable of immobilizing M. incognita J2. The M. incognita J2 exposed to neem and mustard VOCs and inoculated in tomato seedlings resulted in reduced gall formation and nematode reproduction, showing the nematicidal effect of the plant-emitted VOCs. GC/MS analysis revealed the presence of 58 and 32 molecules in the VOCs emitted from neem and mustard macerates, respectively. Alcohols were found in both the neem and mustard VOCs. Esters were found in the neem VOCs, and sulfur-containing compounds, mostly isothiocyanates, were found in mustard. Our results demonstrate that plant VOCs contain diversified molecules that affect M. incognita mobility, pathogenicity and reproduction. Nematode toxic VOCs may be retained in water, which prevents the VOCs from escaping into the air and causing the water to become toxic to nematodes. These data may explain part of the role of VOCs in the biofumigation process, through plant incorporation with the soil, and suggests that irrigation performed directly after incorporation may trap the VOCs in soil water and thereafter retain nematode toxicity longer than incorporation that is performed later.

Emission Characteristics of Particulate Matter and Volatile Organic Compounds in Cow Dung Combustion

Biomass fuel is used for cooking and heating, especially in developing countries. Combustion of biomass fuel can generate high levels of indoor air pollutants, including particulate matter (PM) and volatile organic compounds (VOCs). This study characterized PM and VOC emissions from cow dung combustion in a controlled experiment. Dung from grass-fed cows was dried and combusted using a dual-cone calorimeter. Heat fluxes of 10, 25, and 50 kW/m(2) were applied. The concentrations of PM and VOCs were determined using a dust spectrometer and gas chromatography/mass spectrometry, respectively. PM and VOC emission factors were much higher for the lower heat flux, implying a fire ignition stage. When the heat flux was 50 kW/m(2), the CO2 emission factor was highest and the PM and VOC emission factors were lowest. Particle concentrations were highest in the 0.23-0.3 μm size range at heat fluxes of 25 and 50 kW/m(2). Various toxic VOCs, including acetone, methyl ethyl ketone, benzene, and toluene, were detected at high concentrations. Although PM and VOC emission factors at 50 kW/m(2) were lower, they were high enough to cause extremely high indoor air pollution. The characteristics of PM and VOC emissions from cow dung combustion indicated potential health effects of indoor air pollution in developing countries.

Removal of beta-pinene and limonene using compost biofilter

Composting is widely used for the treatment of solid organic wastes; however, emissions from composting are becoming a threat to humans due to the release of toxic volatile organic compounds (VOCs). VOCs from composting operations are characterized by high flow rates and, normally, low pollutant concentration. Typical VOCs include a large amount of terpenes (∼65% of total VOCs). This study was to investigate the efficiency of biofiltration in controlling terpene emissions from composting operations using a laboratory-scale unit. The performance of a biofilter was investigated as a function of inlet flow rate, inlet concentration, and bed length/bed diameter (L/D) ratio of bed. At the lowest total inlet flow rate, removal efficiency of limonene and β-pinene was more than 90%. With the decrease in inlet concentration and increase in L/D ratio, the removal efficiency was effectively increased. Removal efficiency of more than 85% for Limonene and 45% for β-Pinene was attained at a loading rate of 55 g/m3-hr. The maximum elimination capacity was found for 109.7 g/m3-hr for limonene and 10.3 g/m3-hr for β-pinene at a critical loading of 150.1 g/m3-hr. Based on this study, the compost bed could function as a biofilter for controlling terpene odors during the composting process. Implications: The purpose of this research project is to investigate the efficiency of biofiltration in controlling limonene and β-pinene emissions from composting operations using a laboratory scale. In addition, the performance of a biofilter as a function of inlet flow rate, inlet concentration, and L/D ratio of bed was evaluated. Establishing a nexus between the operational parameters and efficiency would be useful in design and operation of compost bed as a biofilter for controlling terpene odors during the composting process.

Drosophila melanogaster as a model to characterize fungal volatile organic compounds

Fungi are implicated in poor indoor air quality and may pose a potential risk factor for building/mold related illnesses. Fungi emit numerous volatile organic compounds (VOCs) as alcohols, esters, ethers, ketones, aldehydes, terpenoids, thiols, and their derivatives. The toxicity profile of these VOCs has never been explored in a model organism, which could enable the performance of high throughput toxicological assays and lead to a better understanding of the mechanism of toxicity. We have established a reductionist Drosophila melanogaster model to evaluate the toxicity of fungal VOCs. In this report, we assessed the toxicity of fungal VOCs emitted from living cultures of species in the genera, Trichoderma, Aspergillus, and Penicillium and observed a detrimental effect on larval survival. We then used chemical standards of selected fungal VOCs to assess their toxicity on larval and adult Drosophila. We compared the survival of adult flies exposed to these fungal VOCs with known industrial toxic chemicals (formaldehyde [37%], xylene, benzene, and toluene). Among the tested fungal VOC standards, the compounds with eight carbons (C8) caused greater truncation of fly lifespan than tested non-C8 fungal VOCs and industrial toxins. Our data validate the use of Drosophila melanogaster as a model with the potential to elucidate the mechanistic attributes of different toxic VOCs emitted by fungi and also to explore the potential link between reported human illnesses/symptoms and exposure to water damaged and mold contaminated buildings.

BTX abatement using Chilean natural zeolite: the role of Brønsted acid sites

In wastewater treatment facilities, air quality is not only affected by conventional unpleasant odour compounds; toxic volatile organic compounds (VOCs) are also found. In this study, the adsorptive capacity of Chilean natural zeolite toward VOC removal was evaluated. Moreover, the influence of zeolite chemical surface properties on VOC elimination was also investigated. Three modified zeolite samples were prepared from a natural Chilean zeolite (53% clinoptilolite, 40% mordenite and 7% quartz). Natural and modified zeolite samples were characterised by nitrogen adsorption at 77 K, elemental analyses and X-ray fluorescence (XRF). Chemical modifications of natural zeolite showed the important role of Brønsted acid sites on the abatement of VOCs. The presence of humidity has a negative effect on zeolite adsorption capacity. Natural zeolites could be an interesting option for benzene, toluene and xylene vapour emission abatement.

Spatial variability in levels of benzene, formaldehyde, and total benzene, toluene, ethylbenzene and xylenes in New York City: a land-use regression study

BackgroundHazardous air pollutant exposures are common in urban areas contributing to increased risk of cancer and other adverse health outcomes. While recent analyses indicate that New York City residents experience significantly higher cancer risks attributable to hazardous air pollutant exposures than the United States as a whole, limited data exist to assess intra-urban variability in air toxics exposures.MethodsTo assess intra-urban spatial variability in exposures to common hazardous air pollutants, street-level air sampling for volatile organic compounds and aldehydes was conducted at 70 sites throughout New York City during the spring of 2011. Land-use regression models were developed using a subset of 59 sites and validated against the remaining 11 sites to describe the relationship between concentrations of benzene, total BTEX (benzene, toluene, ethylbenzene, xylenes) and formaldehyde to indicators of local sources, adjusting for temporal variation.ResultsTotal BTEX levels exhibited the most spatial variability, followed by benzene and formaldehyde (coefficient of variation of temporally adjusted measurements of 0.57, 0.35, 0.22, respectively). Total roadway length within 100 m, traffic signal density within 400 m of monitoring sites, and an indicator of temporal variation explained 65% of the total variability in benzene while 70% of the total variability in BTEX was accounted for by traffic signal density within 450 m, density of permitted solvent-use industries within 500 m, and an indicator of temporal variation. Measures of temporal variation, traffic signal density within 400 m, road length within 100 m, and interior building area within 100 m (indicator of heating fuel combustion) predicted 83% of the total variability of formaldehyde. The models built with the modeling subset were found to predict concentrations well, predicting 62% to 68% of monitored values at validation sites.ConclusionsTraffic and point source emissions cause substantial variation in street-level exposures to common toxic volatile organic compounds in New York City. Land-use regression models were successfully developed for benzene, formaldehyde, and total BTEX using spatial indicators of on-road vehicle emissions and emissions from stationary sources. These estimates will improve the understanding of health effects of individual pollutants in complex urban pollutant mixtures and inform local air quality improvement efforts that reduce disparities in exposure.

Photocatalytic performance of cylindrical reactor inserted with UV light-emitting-diodes for purification of low-level toxic volatile organic compounds

The present study investigated the photocatalytic performance of a cylindrical reactor inserted with UV light-emitting-diodes for the decomposition of low-level (0.1ppm) gas-phase organic compounds (benzene, toluene, ethyl benzene and xylene (BTEX)). The morphological and optical properties of photocatalysts (Degussa P-25 TiO2) baked at different temperatures were determined using a range of spectral instruments. The photocatalyst baked at 350°C exhibited the highest conversion efficiencies for both benzene and toluene (81 and ∼100%, respectively). The conventional lamp showed a higher conversion efficiency for benzene compared to the 380-nm UV-LED and a higher conversion efficiency for benzene and toluene than the 365-nm UV-LED. However, the ratios of conversion efficiency to electric power consumption were 2.5–3.0 times higher for the latter light source than the former source. Moreover, as the residence time increased from 0.2 to 1.2min, the average conversion efficiencies for BTEX of the 3-h photocatalytic process increased from nearly zero to 81%, 7 to nearly 100%, 20 to nearly 100%, and 29–30 to nearly 100%, respectively. The cylindrical photocatalytic reactor inserted with UV-LEDs could be energy-efficiently applied for the decomposition of low-level toxic compounds after optimization of the operating conditions.

CuO/zeolite catalyzed oxidation of gaseous toluene under microwave heating

The development of a combined process of catalytic oxidation and microwave heating for treatment of toluene waste gas was described in this work. Toluene, a typical toxic volatile organic compound, was oxidized through a fixed bed reaction chamber containing zeolite-supported copper oxide (CuO/zeolite) catalyst mixed with silicon carbide (SiC), an excellent microwave-absorbing material. The target compound was efficiently degraded on the surface of the catalyst at high reaction temperature achieved by microwave-heated SiC. A set of experimental parameters, such as microwave power, air flow and the loading size of CuO etc., were investigated, respectively. The study demonstrated these parameters had critical impact on toluene degradation. Under optimal condition, 92% toluene was removed by this combined process, corresponding to an 80%–90% TOC removal rate. Furthermore, the catalyst was highly stable even after eight consecutive 6-h runs. At last, a hypothetical degradation pathway of toluene was proposed based on the experimental data obtained from gas chromatography-mass spectrum and Fourier transform infrared spectroscopy analyses.

Removal of mixture of VOCs by nonthermal plasma

Nonthermal plasma treatment is one of the promising air-cleaning technologies to remove dilute volatile organic compounds (VOCs) in air. Present study deals with the removal of dilute VOCs mixture in a dielectric barrier discharge reactor with sintered metal fiber as the inner electrode. Electrical characterization of the reactor including the experimental system and the reactor design has been studied. Typical results during abatement of VOCs mixture of n-propanol, p-xylene, and Dioxane (DOX) highlighted the potential of the plasma processing to decompose toxic VOCs. It has been observed that the order of removal efficiency of VOCs follows n-propanol > p-xylene > DOX, which explain their chemical bond strength and molecule stability.