Volatile Organic Gases Research Articles

γ-irradiation induced zinc ferrites and their enhanced room-temperature ammonia gas sensing properties

Zinc ferrite (ZnFe2O4) nanoparticles (NPs), synthesized using a facile and cost-effective sol-gel auto-combustion method, were irradiated with 2 and 5 kGy γ-doses using 60Co as a radioactive source. Effect of γ-irradiation on the structure, morphology, pore-size and pore-volume and room-temperature (300 K) gas sensor performance has been measured and reported. Both as-synthesized and γ-irradiated ZnFe2O4 NPs reveal remarkable gas sensor activity to ammonia in contrast to methanol, ethanol, acetone and toluene volatile organic gases. The responses of pristine, 2 and 5 kGy γ-irradiated ZnFe2O4 NPs are respectively 55%, 66% and 81% @100 ppm concentration of ammonia, signifying an importance of γ-irradiation for enhancing the sensitivity, selectivity and stability of ZnFe2O4 NPs as ammonia gas sensors. Thereby, due to increase in surface area and crystallinity on γ-doses, the γ-irradiation improves the room-temperature ammonia gas sensing performance of ZnFe2O4.

Risk Analysis and Assessment to Enhance Safety in a Smart Kitchen

Cooking activity is accompanied with several risks, mainly for elderly people due to attention and memory impairment. Literature reveals that the kitchen is the second most common place for domestic accidents. We argue that enhancing safety during cooking activities could be achieved via designing a cooking-safe environment based on insightful risk analysis and assessment study. This paper presents our study on risk analysis and assessment during cooking, in order to build a cooking-safe environment. The study is based on theoretical and real-world experimentations. Risk analysis and assessment enabled us to determine the three major risks (i.e., fire, burn and intoxication by gas/smoke) and the pertinent parameters to quantify these risks. The results reveal that the pertinent parameters are: concentrations of volatile organic compounds, alcohol, and carbon monoxide gases in the cooking smoke, utensil temperature, burner temperature, relative humidity, and presence of a utensil on burner. We present in details our study on risk analysis and assessment, including the methodology and the findings.

Sensing and capture of toxic and hazardous gases and vapors by metal-organic frameworks.

Toxic and hazardous chemical species are ubiquitous, predominantly emitted by anthropogenic activities, and pose serious risks to human health and the environment. Thus, the sensing and subsequent capture of these chemicals, especially in the gas or vapor phase, are of extreme importance. To this end, metal-organic frameworks have attracted significant interest, as their high porosity and wide tunability make them ideal for both applications. These tailorable framework materials are particularly promising for the specific sensing and capture of targeted chemicals, as they can be designed to fit a diverse range of required conditions. This review will discuss the advantages of metal-organic frameworks in the sensing and capture of harmful gases and vapors, as well as principles and strategies guiding the design of these materials. Recent progress in the luminescent detection of aromatic and aliphatic volatile organic compounds, toxic gases, and chemical warfare agents will be summarized, and the adsorptive removal of fluorocarbons/chlorofluorocarbons, volatile radioactive species, toxic industrial gases and chemical warfare agents will be discussed.

Chromate membrane generation of volatile organic compounds standard gas mixtures at the ppm level

Chromate membrane generation of volatile organic compounds standard gas mixtures at the ppm level

Electrospinning Hetero-Nanofibers In₂O₃/SnO₂ of Homotype Heterojunction with High Gas Sensing Activity.

In2O3/SnO2 composite hetero-nanofibers were synthesized by an electrospinning technique for detecting indoor volatile organic gases. The physical and chemical properties of In2O3/SnO2 hetero-nanofibers were characterized and analyzed by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), Energy Dispersive X-Ray Spectroscopy (EDX), specific surface Brunauer–Emmett–Teller (BET) and X-ray photoelectron spectroscopy (XPS). Gas sensing properties of In2O3/SnO2 composite hetero-nanofibers were measured with six kinds of indoor volatile organic gases in concentration range of 0.5~50 ppm at the operating temperature of 275 °C. The In2O3/SnO2 composite hetero-nanofibers sensor exhibited good formaldehyde sensing properties, which would be attributed to the formation of n-n homotype heterojunction in the In2O3/SnO2 composite hetero-nanofibers. Finally, the sensing mechanism of the In2O3/SnO2 composite hetero-nanofibers was analyzed based on the energy-band principle.

An optical fiber taper fluorescent probe for detection of nitro-explosives based on tetraphenylethylene with aggregation-induced emission

Abstract In this work, we report a novel optical fiber taper fluorescent probe for detection of nitro-explosives. The probe was fabricated by an in-situ photo-plating through evanescent wave and transmitted light initiated thiol-ene “click” reaction, from which a cross-linked fluorescence porous polymer film was covalently bonded on the surface of the fiber taper. The film exhibits well-organized porous structure due to the presence of polyhedral oligomeric vinylsilsesquioxane moieties, and simultaneously displays strong fluorescence from tetraphenylethylene with aggregation-induced emission property. These two characters make the probe show a remarkable sensitivity, anti-photo-bleaching and a repeatability in detection of TNT and DNT vapors by fluorescence quenching. In addition, the detection is not interfered in the presence of other volatile organic gases.

The MERMAID study: indoor and outdoor average pollutant concentrations in 10 low‐energy school buildings in France

Indoor air quality was characterized in 10 recently built energy-efficient French schools during two periods of 4.5days. Carbon dioxide time-resolved measurements during occupancy clearly highlight the key role of the ventilation rate (scheduled or occupancy indexed), especially in this type of building, which was tightly sealed and equipped with a dual-flow ventilation system to provide air refreshment. Volatile organic compounds (VOCs) and inorganic gases (ozone and NO2 ) were measured indoors and outdoors by passive techniques during the occupied and the unoccupied periods. Over 150 VOC species were identified. Among them, 27 species were selected for quantification, based on their occurrence. High concentrations were found for acetone, 2-butanone, formaldehyde, toluene, and hexaldehyde. However, these concentrations are lower than those previously observed in conventional school buildings. The indoor/outdoor and unoccupied/occupied ratios are informative regarding emission sources. Except for benzene, ozone, and NO2 , all the pollutants in these buildings have an indoor source. Occupancy is associated with increased levels of acetone, 2-butanone, pentanal, butyl acetate, and alkanes.

High-yield exfoliation of graphene using ternary-solvent strategy for detecting volatile organic compounds

Despite the great progress in the theory and experimental verification we made in past decade, the practical application of graphene is still hindered by the lack of efficient, economical, scalable, ease-processing exfoliation method. Herein, we propose a facile, low-cost, and efficient liquid-phase exfoliation process using low boiling-temperature solvent mixture to fabricate few-layer graphene in large scale. The Hansen solubility parameter theory was applied to help optimize the composition of solvent mixture. Aqueous-based ternary-solvent mixture, for the first time, was adapted to exfoliate graphene. We demonstrate that the exfoliation efficiency using ternary-solvent mixture surpasses that from binary-solvent approach. The final product concentration after optimization was over 260μg/ml. The concentrated graphene dispersion was used to fabricate gas sensor for detecting volatile organic gases. Taking advantage of large surface area, large number of adsorption sites, and well-preserved basal plane, the mass-produced graphene nanosheets exhibited promising sensing potential toward ethanol and methanol vapors.

Industrial odor sources and air pollutant concentrations in Globeville, a Denver, Colorado neighborhood

An odor of unknown origin described as a “tar” or “asphalt” smell has become unbearable for many of Globeville, CO, residents over the past few years. Residents report during odor events burning eyes and throat, headaches, skin irritation, and problems sleeping. This study was undertaken to identify the potential sources of the odor and the concentrations of air pollutants making up the odor by conducting meteorological correlations and sampling for a panel of volatile organic compounds (VOCs), sulfur gases, and polycyclic aromatic hydrocarbons (PAHs) in the neighborhood and near suspected sources. Wind speed and direction data collected every 1 min in the neighborhood indicate that when the odor is noticed, the community is directly downwind of a wood preservation facility and an asphalt roofing facility. Air samples collected during high-intensity odor events have shown concentrations of methylene chloride, hexane, toluene, naphthalene, dibenz[a,h]anthracene, benzo[g,h,i]perylene, and indeno[1,2,3-cd]pyrene, each at least two times higher than background concentrations. Naphthalene and the other PAHs are known pollutants emitted from wood treatment processes, and are known to have a coal tar odor. Naphthalene was present in a sample collected directly adjacent to the Koppers facility and was not present in any background samples. Single-compound odor and health thresholds, however, were never surpassed. Given the technical and regulatory challenges of sampling odors and controlling emissions, it is recommended that Globeville residents and neighboring industry pursue a “good neighbor policy” to solve the odor issue. Specific offending industrial processes could be identified for which there exist cost-effective control technologies that would reduce exposure to odors and air toxics in Globeville.Implications: Meteorological correlations and samples of volatile organic compounds (VOCs), sulfur gases, and polycyclic aromatic hydrocarbons (PAHs) in the Globeville, CO, neighborhood and near suspected sources during odor events indicate potential industrial sources of a transient and noxious odor. Legislative approaches have proven unfruitful and no health or odor thresholds were typically violated. New approaches are warranted to address odor mixture effects in neighborhoods near industrial facilities.

Emission of Volatile Organic Compounds and Greenhouse Gases from the Aerobic Bioremediation of Soils Contaminated with Diesel

Bioremediation processes have been credited for reducing high levels of organic contaminants from soils. However, during the bioremediation of soils contaminated with diesel, the conversion of heavy molecules to volatile organic compounds (VOCs) and greenhouse gases (GHGs) and the volatilization of light molecules can occur. The ongoing construction of a large petrochemical complex in Rio de Janeiro (COMPERJ) and the transportation of large volumes of oil by-products have raised serious concerns regarding accidents that may result in soil contamination. Bioremediation is a potential technique that can be applied to minimize damage from such contamination. The objective of this study was to characterize the emission of GHGs and VOCs during the bioremediation of soils contaminated with diesel oil. Soil samples contaminated with 0.5, 2.0, and 4.0 w/w% diesel oil were kept in glass rectors (2 L internal volume) for 3 months under anaerobic/anoxic conditions. The soil moisture was kept at 80 % of the field capacity. Bioremediation processes were investigated in regard to nutrient adjustment (biostimulation), no adjustment (natural attenuation), and sterilized soil (abiotic process). The gases emitted from various reactors were collected with coconut shell charcoal cartridges, and the GHGs were collected in Tedlar bags. The chemical analyses of GHGs and VOCs were performed using gas chromatography. The results indicated that air samples contained high concentrations of CO2, but low concentrations of CH4. Differences in the composition of the gas emitted, regarding CO2, were not statistically significant. Regarding VOC emissions, such as alkanes and alkenes (both branched), cycloalkanes, and aromatic-substituted compounds, the compounds with higher emissions were cycloalkanes and branched alkanes.

Aqueous organic chemistry in the atmosphere: sources and chemical processing of organic aerosols.

Over the past decade, it has become clear that aqueous chemical processes occurring in cloud droplets and wet atmospheric particles are an important source of organic atmospheric particulate matter. Reactions of water-soluble volatile (or semivolatile) organic gases (VOCs or SVOCs) in these aqueous media lead to the formation of highly oxidized organic particulate matter (secondary organic aerosol; SOA) and key tracer species, such as organosulfates. These processes are often driven by a combination of anthropogenic and biogenic emissions, and therefore their accurate representation in models is important for effective air quality management. Despite considerable progress, mechanistic understanding of some key aqueous processes is still lacking, and these pathways are incompletely represented in 3D atmospheric chemistry and air quality models. In this article, the concepts, historical context, and current state of the science of aqueous pathways of SOA formation are discussed.

Gaseous chemical compounds in indoor and outdoor air of 602 houses throughout Japan in winter and summer

A nationwide survey of indoor air quality in Japan was conducted using four types of diffusive samplers. Gaseous chemical compounds such as carbonyls, volatile organic compounds (VOC), acid gases, basic gases, and ozone were measured in indoor and outdoor air of 602 houses throughout Japan in winter and summer. Four kinds of diffusive samplers were used in this study: DSD-BPE/DNPH packed with 2,4-dinitrophenyl hydrazine and trans-1,2-bis(2-pyridyl)ethylene coated silica for ozone and carbonyls; VOC-SD packed with Carboxen 564 particles for volatile organic compounds; DSD-TEA packed with triethanolamine impregnated silica for acid gases; and DSD-NH3 packed with phosphoric acid impregnated silica for basic gases. These samplers are small and lightweight and do not require a power source, hence, it was possible to obtain a large number of air samples via mail from throughout Japan. Almost all compounds in indoor air were present at higher levels in summer than in winter. In particular, formaldehyde, toluene, and ammonia were strongly dependent on temperature, and their levels increased with temperature. The nitrogen dioxide concentration in indoor air particularly increased only during winter and was well correlated with the formic acid concentration (correlation coefficient=0.959). Ozone concentrations in indoor air were extremely low compared with the outdoor concentrations. Ozone flowing from outdoor air may be decomposed quickly by chemical compounds in indoor air; therefore, it is suggested that the indoor/outdoor ratio of ozone represents the ventilation of the indoor environment.

Measurement of Chemical Compounds in Indoor and Outdoor Air in Chiba City Using Diffusive Sampling Devices

Indoor air quality (IAQ) is a major concern, because people on average spend the vast majority of their time indoors and they are repeatedly exposed to indoor air pollutants. In this study, to assess indoor air quality in Chiba City, gaseous chemical compounds were surveyed using four types of diffusive sampler. Gaseous chemical compounds such as carbonyls, volatile organic compounds (VOC), acid gases, basic gases, and ozone were measured in indoor and outdoor air of 50 houses throughout Chiba City in winter and summer. Four types of diffusive sampler were used in this study: DSD-BPE/DNPH packed with 2,4-dinitrophenyl hydrazine and trans-1,2-bis(2-pyridyl)ethylene-coated silica for ozone and carbonyls; VOC-SD packed with Carboxen 564 particles for volatile organic compounds; DSD-TEA packed with triethanolamine-impregnated silica for acid gases; and DSD-NH3 packed with phosphoric acid-impregnated silica for basic gases. Almost all compounds in indoor air were detected at higher concentrations in summer than in winter. However, the nitrogen dioxide concentration in indoor air particularly increased only in winter, which well correlated with the formic acid concentration (correlation coefficient=0.974). The compound with the highest concentrations in indoor air was p-dichlorobenzene, with recorded levels of 13,000 μg m(-3) in summer and 1,100 μg m(-3) in winter in indoor air. p-Dichlorobenzene in summer and nitrogen dioxide in winter are detected at markedly high concentrations. Pollution control and continuous monitoring of IAQ are indispensable for human health.

4種の拡散サンプラーを用いる札幌市における屋内外のガス状化学物質の実態調査

Gaseous chemical compounds such as carbonyls, volatile organic compounds (VOC), acid gases, basic gases, and ozone were measured in indoor and outdoor air of 40 houses throughout Sapporo city in the winter (January to March, 2012 and 2013) and summer (July to September, 2012) using four kinds of diffusive samplers. Almost all compounds in indoor air were present at higher levels in the summer than in the winter. The indoor concentrations of acetaldehyde and p-dichlorobenzene exceeded the Health, Labour and Welfare, Japan guideline in three and two houses, respectively. The mean concentrations of formaldehyde were 27 μg m−3 in the summer and 17 μg m−3 in the winter, and showed that the summer concentration was 1.6-fold higher than that in the winter. Nitrogen dioxide was present in extremely high concentrations in the winter, and it was suggested that the sources of nitrogen dioxide in indoor air are kerosene heaters, unvented gas stoves and heaters. Formic acid was generated by combustion because the nitrogen dioxide concentration in indoor air was well correlated with the formic acid concentration (correlation coefficient = 0.947). In outdoor air, the negative correlation between nitrogen dioxide and ozone was observed during the winter. It was suggested that the reaction of nitric oxide and ozone may influence the formation of nitrogen dioxide.

Effects of trichloroethylene on community structure and activity of methanotrophs in landfill cover soils

Landfill cover soil (LCS) plays an important role in mitigating the emission of CH4 and volatile organic gases from landfills to the atmosphere. In this study, effect of trichloroethylene (TCE) on community structure and activity of methanotrophs, as well as TCE degradation efficiency was investigated in waste biocover soil (WBS), which was collected from a landfill bioreactor treating organic waste, in comparison with LCS. The CH4 oxidation activity and TCE degradation rate were higher in WBS compared to those in LCS. The TCE degradation rates in both soils were enhanced with the increase of TCE concentration within 50 ppmv. Compared to LCS, the TCE inhibitory concentration that caused inhibition of CH4 oxidation activity was greater for WBS. The abundance of mmoX was similar in both soils during the whole experiment, while the average abundance of pmoA in WBS was about two orders of magnitudes higher than in LCS. Type I methanotrophs (Methylocaldum, Methylomonas, Methylosarcina and Methylobacter) and type II methanotrophs (Methylocystis) were abundant in both soils. Among them, type I methanotrophs Methylocaldum and Methylobacter dominated in WBS, while type II methanotrophs Methylocystis predominated in LCS. The relative abundance of Methylobacter increased with an increase of TCE concentration and exposure time in both soils, especially in WBS, indicating that Methylobacter seemed tolerant to TCE and/or may play an important role in the TCE degradation.

Human Health Risk Assessment of a landfill based on volatile organic compounds emission, immission and soil gas concentration measurements

A Human Health Risk Assessment (HHRA) was required for a closed landfill located in Cerdanyola del Vallès (Barcelona, Spain). The HHRA had two objectives, to evaluate the present risk of the identified receptors in the area and to safely develop the future urban planning of the area, therefore 3 scenarios for the current situation and 4 for the future situation were developed.After reviewing the existing data and exploring the needs of information, the assessment in this study was focused on the measurement of volatile organic compounds (VOCs) fluxes from the subsoil (emission from the landfill at 5 points), concentrations of VOCs in the air (immission in 4 urban sites) and concentration of VOCs in soil–gas (measurements at 5m below ground surface outside the landfill at 8 sites). Around 70 VOCs were analyzed by using multi-sorbent tubes and Thermal Desorption Gas Chromatography (TD–GC–MS). The VOCs that were detected and quantified include alkanes, aromatic hydrocarbons, alcohols, ketones, halocarbons, aldehydes, esters, terpenoids, ethers and some nitrogenated and sulfur compounds, furans and carboxylic acids. Specific mercury flux measurements were performed in a hot spot by using carulite tubes, that were also analyzed by using Thermal Decomposition, Amalgamation, and Atomic Absorption Spectrophotometry.Results showed average values of volatile emission fluxes ranging from non-detected to 331μgm−2day−1 (dichlorodifluoromethane). In the case of immission, the concentration of VOCs measured in the air of populated area surrounding the landfill ranged values from non-detected to 42.0μgm−3 (acetic acid). The soil–gas measurements in piezometers around the landfill showed individual VOC values with a maximum 830μgm−3 for dichlorodifluoromethane.With the obtained fluxes and concentrations in air and soil–gas, USEPA methodology and modeling was used to evaluate equivalent concentration in the scenarios considered. Toxicity values from IRIS database were used to finally obtain chemical risk indicators. Admissible risk indicators were obtained in all scenarios. The VOCs that contributed more to risk indexes in RH2 were trichloroethylene, trimethylbenzene, chloroform, 1,2-dichloroethane and carbon tetrachloride. The carcinogenic risk in RH7 was linked to the presence of benzene and chloroform. The comparison of the measurements of the present work with other landfills evidence that HHRA in ambient air would be needed in order to perform a correct landfill management.

Diffusion of volatile organics through porous snow: impact of surface adsorption and grain boundaries

Abstract. Release of trace gases from surface snow on earth drives atmospheric chemistry, especially in the polar regions. The gas-phase diffusion of methanol and of acetone through the interstitial air of snow was investigated in a well-controlled laboratory study in the temperature range of 223 to 263 K. The aim of this study was to evaluate how the structure of the snowpack, the interaction of the trace gases with the snow surface, and the grain boundaries influence the diffusion on timescales up to 1 h. The diffusive loss of these two volatile organics into packed snow samples was measured using a chemical ionization mass spectrometer. The structure of the snow was analysed by means of X-ray-computed micro-tomography. The observed diffusion profiles could be well described based on gas-phase diffusion and the known structure of the snow sample at temperatures ≥ 253 K. At colder temperatures, surface interactions start to dominate the diffusive transport. Parameterizing these interactions in terms of adsorption to the solid ice surface, i.e. using temperature-dependent air–ice partitioning coefficients, better described the observed diffusion profiles than the use of air–liquid partitioning coefficients. No changes in the diffusive fluxes were observed by increasing the number of grain boundaries in the snow sample by a factor of 7, indicating that for these volatile organic trace gases, uptake into grain boundaries does not play a role on the timescale of diffusion through porous surface snow. For this, a snow sample with an artificially high amount of ice grains was produced and the grain boundary surface measured using thin sections. In conclusion, we have shown that the diffusivity can be predicted when the structure of the snowpack and the partitioning of the trace gas to solid ice is known.

Highly Sensitive and Selective Gas Sensor Using Hydrophilic and Hydrophobic Graphenes

New hydrophilic 2D graphene oxide (GO) nanosheets with various oxygen functional groups were employed to maintain high sensitivity in highly unfavorable environments (extremely high humidity, strong acidic or basic). Novel one-headed polymer optical fiber sensor arrays using hydrophilic GO and hydrophobic reduced graphene oxide (rGO) were carefully designed, leading to the selective sensing of volatile organic gases for the first time. The two physically different surfaces of GO and rGO could provide the sensing ability to distinguish between tetrahydrofuran (THF) and dichloromethane (MC), respectively, which is the most challenging issue in the area of gas sensors. The eco-friendly physical properties of GO allowed for faster sensing and higher sensitivity when compared to previous results for rGO even under extreme environments of over 90% humidity, making it the best choice for an environmentally friendly gas sensor.

A Novel Tool for Noninvasive Diagnosis and Tracking of Patients with Inflammatory Bowel Disease

The pathogenesis of inflammatory bowel disease (IBD) involves the role of bacteria. These bacteria ferment nonstarch polysaccharides in the colon producing a fermentation profile that through altered gut permeability can be traced in urine. We proposed to track the resultant volatile organic compounds or gases that emanate from urine using noninvasive real-time tools, specifically by electronic nose and Field Asymmetric Ion Mobility Spectrometer (FAIMS) instruments. The aim of this study was to determine the utility of electronic nose and FAIMS instruments to detect and track the fermentation profile of patients with IBD. Sixty-two individuals were recruited, 48 individuals with IBD (24 with Crohn's disease and ulcerative colitis, respectively) and 14 controls. The disease activity was recorded, and urine samples were collected. The headspace (the air above the sample) was analyzed using the electronic nose and FAIMS instruments. Electronic nose data analysis was conducted through (1) Principal Component Analysis (data were analyzed together without previous categorization); and (2) Discriminant Function Analysis (samples were precategorized [clinical groups]). The FAIMS data were processed by Fisher's Discriminant Analysis (precategorized [clinical groups]). Both technologies consistently showed the ability to separate those with IBD and controls with a >75% accuracy; P < 0.001. In a smaller subgroup (n = 24), we also demonstrated that the electronic nose and FAIMS instruments can distinguish between active disease and those in remission. The fermentation profile or fermentome is disparate in those with IBD compared with controls--a reflection of the bacterial diversity in health and disease. This profile also changes (and was tracked) as the disease is induced into remission. Thus, the electronic nose and FAIMS instruments offer the potential of a noninvasive real-time diagnostic tool for point of care clinical use.

Preparation and characterization of hydrophobic porphyrin nanoaggregates dispersed in polyvinyl alcohol films

It is known that among other applications porphyrin aggregates can be used in the detection of volatile organic compounds (VOC) and gases and vapors in general. However, the use of porphyrins for this purpose has been limited by the fact that usually the porphyrin and the polymer employed as a matrix are soluble in different media, such as polyvinyl alcohol and tetraphenylporphyrin, respectively. In this paper, we discuss how starting from stable aqueous solutions of hydrophobic porphyrins one can use the drop coating method to prepare polyvinyl alcohol polymer matrices containing porphyrin aggregates. The resulting solid films were characterized by optical techniques, and we have used UV-vis absorption spectroscopy to analyze how they interact with vapors of HCl , NO2 and NH3 .