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At least 163 records · Page 9Linked to original sources
PubMed1991

Biofiltration: an innovative air pollution control technology for VOC emissions.

Biofiltration is a relatively recent air pollution control (APC) technology in which off-gases containing biodegradable volatile organic compounds (VOC) or inorganic air toxics are vented through a biologically active material. This technology has been successfully applied in Germany and The Netherlands in many full-scale applications to control odors, VOC and air toxic emissions from a wide range of industrial and public sector sources. Control efficiencies of more than 90 percent have been achieved for many common air pollutants. Due to lower operating costs, biofiltration can provide significant economic advantages over other APC technologies if applied to off-gases that contain readily biodegradable pollutants in low concentrations. Environmental benefits include low energy requirements and the avoidance of cross media transfer of pollutants. This paper reviews the history and current status of biofiltration, outlines its underlying scientific and engineering principles, and discusses the applicability of biofilters for a wide range of specific emission sources.

Air Pollution↗
PubMed1995

Evaluation of VOC emission measurement methods for paint spray booths.

Interest in regulations to control solvent emissions from automotive painting systems is increasing, especially in ozone nonattainment areas. Therefore, an accurate measurement method for VOC emissions from paint spray booths used in the automotive industry is needed to ascertain the efficiency of the spray booth capture and the total emissions. This paper presents the results of a laboratory study evaluating potential VOC sampling and analytical methods used in estimating paint spray booth emissions, and discusses these results relative to other published data. Eight test methods were selected for evaluation. The accuracy of each sampling and analytical method was determined using test atmospheres of known concentration and composition that closely matched the actual exhaust air from paint spray booths. The solvent mixture to generate the test atmospheres contained a large proportion of polar, oxygenated hydrocarbons such as ketones and alcohols. A series of identical tests was performed for each sampling/analytical method with each test atmosphere to assess the precision of the methods. The study identified significant differences among the test methods in terms of accuracy, precision, cost, and complexity.

Air Pollutants↗
PubMed2002

Online hourly determination of 62 VOCs in ambient air: system evaluation and comparison with another two analytical techniques.

This paper presents results of the processing and validation of data collected by an automatic gas chromatograph (AGC). This system was used to monitor 62 volatile organic compounds (VOCs) in urban air in the Basque Country, Spain. The nonpolar compounds (C2-C10) identified-paraffins, olefins, aromatics, and chlorinated compounds-accounted for 88% of the mass of total non-methane hydrocarbons (TNMHCs) in ambient air. The evaluation of linearity, precision, detection limits (DLs), and stability of retention times (RTs) indicates that the equipment is suitable for measuring ambient air automatically for prolonged periods (6 months). The calibration of the equipment using response factors calculated on the basis of the effective carbon number (ECN) showed variations of over 10% for acetylene, isoprene, and n-hexane. The results provided by the automatic chromatograph correlated significantly with simultaneous results from other widely used techniques for determining VOCs in ambient air: (1) portable GC, equipped with photoionization detector (PID), and (2) active adsorption on Tenax-TA followed by thermal desorption and chromatographic analysis.

Air Pollutants↗
PubMed1999

Chamber assessment of formaldehyde and VOC emissions from wood-based panels.

Volatile organic emissions from particleboard, medium density fibreboard (MDF) and office furniture have been measured in dynamic environmental chambers, both small and room-sized. Characterisation of product emission properties in small chambers was possible when inter- and intra-sheet variations were considered. Formaldehyde emission factors for all products were approximately double European low-emission specifications and did not decay to the latter for several months. Long-term emission behaviour could not be predicted from short-term measurements. Volatile organic compounds (VOC) emissions were low for the MDF product, higher for particleboard, and highest for laminated office furniture. The compounds emitted differed from those reported in other countries. VOC emissions from the sheet products decreased more quickly than formaldehyde, reaching low levels within two weeks, except for MDF which was found to become a low-level source of hexanal after several months.

Air Pollution, Indoor↗
PubMed2001

Modeling the removal of VOC mixtures in biotrickling filters.

A mathematical model was derived for describing removal of mixed VOC vapors in biotrickling filters (BTFs). The model accounts for potential process rate limitation by the availability of oxygen as well as for potential kinetic interactions among pollutants during their biodegradation. Without using any fitted parameter, the model was found capable of predicting experimentally obtained removal rates of mono-chlorobenzene (m-CB) and ortho-dichlorobenzene (o-DCB) vapors. Experimental results reported here show that m-CB removal is better than that of o-DCB. The two compounds were known to be involved in a kinetic cross-inhibition interaction when degraded in suspended culture. However, model sensitivity studies showed that cross-inhibition does not affect BTF performance due to the low pollutant concentrations involved. For the same reason, the influence of oxygen on BTF performance was found to be minimal under the conditions tested. The model was found to predict experimentally obtained values with less than 10% error in the majority of cases. Computations with an earlier model describing VOC removal in conventional biofilters showed that, for the model mixture used in this study (m-CB/o-DCB), removal rates obtained with BTFs are one to more than two orders of magnitude higher than those obtained with conventional biofilters. This is attributed to the larger active specific biofilm surface area in BTFs, obtained through the creation of favorable growth conditions for the biomass, and better moisture control.

Air Pollutants↗
PubMed2002

[Kinetic model and simulation of the adsorption-biofilm theory for the process of biopurifying VOC waste gases].

For the process of biopurifying waste gas containing VOC in low concentration by using a biological trickling filter, the related kinetic model and simulation of the new Adsorption-Biofilm theory were investigated in this study. By using the lab test data and the industrial test data, the results of contrast and validation indicated that the model had a good applicability for describing the practical bio-purification process of VOC waste gas. In the simulation study for the affection of main factor, such as the concentration of toluene in inlet gas, the gas flow and the height of biofilm-packing, a good pertinence was showed between calculated data and test dada, the interrelation coefficients were in 0.80-0.97.

Adsorption↗
PubMed2002

[Photocatalytic oxidation of airborne VOCs on TiO2].

Titanium dioxide(TiO2) was used to catalyze the photolysis of benzene, xylene, n-heptane, methanol, acetone, ethylether, formaldehyde, trichloroethylene and perchloroethlene in air. The photolysis was carried out with a high pressure mercury lamp. The degradation rate of these VOCs was more than 80 percent in five minuts except formaldehyde. The effects of catalyst amount, different types of TiO2 catalyst and density of UV on the degradation rate of the VOCs were also studied.

Air Pollution↗
PubMed2004

Volatile organic compound (VOC) analysis and sources of limonene, cyclohexanone and straight chain aldehydes in axenic cultures of Calothrix and Plectonema.

The volatile organic compounds (VOCs) in four standing cultures of axenic benthic cyanobacteria (Calothrix and Plectonema) were studied by GC/MS analysis. To verify the biogenic origin of the VOCs, 13C-labelling experiments were performed, and the differences in labelling were used to differentiate between biogenic and non-biogenic sources. Strongly labelled biogenic compounds were derived from the shikimate (cresol, skatole), isoprenoid (beta-cyclocitral, beta-ionone, geosmin) and fatty acid pathways (5Z-heptadecene, 3-octanone, 1-hexanol). New odour compounds derived from microorgansims were beta-cyclogeraniol, dihydro-beta-ionone and 2-hydroxy-2,6,6-trimethylcyclohexanone. The latter compound had already been found in lake water, but could not be assigned to a particular organism. Straight chain aldehydes (octanal, nonanal, decanal), cyclohexanone, cyclohexanol and limonene were unlabelled beyond their natural isotope ratio. Therefore, the biogenic origin of these compounds is doubtful despite their occurrence in axenic cultures. The observation that limonene was a racemate supports this view. The precursors and reactions that lead to the formation of these non-biogenic compounds are unknown and it may be that they are formed by the analytical procedures rather than then being present in the culture medium.

Aldehydes↗
PubMed2003

Study of VOC distribution in citrus fruits by chromatographic analysis.

The contamination of various parts of citrus fruits by toluene (a representative of volatile organic compounds-VOCs) was analyzed. The model of contamination distribution, based on investigations of the sorption and accumulation of toluene in particular parts of citrus fruits was considered. Solvent extraction of components from fruit parts (waxy layer, cuticle, and pulp) was applied. The extracts were analyzed by gas chromatography. The sorption time profiles for such citrus fruits as kumquats and mandarins were determined by plotting the extracted mass, or the relationship C/C(0), versus the sorption time of toluene. After the sorption process the highest concentration of toluene was observed in the flavedo, where the oil glands of kumquats and mandarins are located. The data obtained prove that the high dissolution of aromatic hydrocarbons results from the presence of essential oils in the oil glands. The diffusion coefficients of toluene for the cuticle and pulp of kumquats were also calculated. The results of model investigations were compared with the actual concentration of toluene in kumquats, citrons, mandarins and oranges from outdoor stands and orchards.

Absorption↗
PubMed2006

Improvement of HS-SPME for analysis of volatile organic compounds (VOC) in water samples by simultaneous direct fiber cooling and freezing of analyte solution.

The sensitivity and precision of headspace solid-phase micro extraction (HS-SPME) at an analyte solution temperature (T (as)) of +35 degrees C and a fiber temperature (T (fiber)) of +5 degrees C were compared with those for HS-SPME at T (as) and T (fiber) of -20 degrees C for analysis of the volatile organic compounds benzene, 1,1,1-trichloroethane, trichloroethylene, toluene, o-xylene, ethylbenzene, m/p-xylene, and tetrachloroethylene in water samples. The effect of simultaneous fiber cooling and analyte solution freezing during extraction was studied. The compounds are of different hydrophobicity, with octanol/water partition coefficients (Kow) ranging from 126 and 2511. During a first set of experiments the polydimethylsiloxane (PDMS) SPME fiber was cooled to +5 degrees C with simultaneous heating of the aqueous analyte solution to +35 degrees C. During a second set of experiments, both SPME fiber holder and samples were placed in a deep freezer maintained at -20 degrees C for a total extraction time of 30 min. After approximately 2 min the analyte solution in the vial began to freeze from the side inwards and from the bottom upwards. After approximately 30 min the solution was completely frozen. Analysis of VOC was performed by coupling HS-SPME to gas chromatography-mass spectrometry (GC-MS). In general, i.e. except for tetrachloroethylene, the sensitivity of HS-SPME increased with increasing compound hydrophobicity at both analyte solution and fiber temperatures. At T (as) of +35 degrees C and T (fiber) of +5 degrees C detection limits of HS-SPME were 0.5 microg L(-1) for benzene, 1,1,1-trichloroethane, trichloroethylene, and tetrachloroethylene, 0.125 microg L(-1) for toluene, and 0.025 microg L(-1) for ethylbenzene, m/p-xylene, and o-xylene. In the experiments with T (as) and T (fiber) of -20 degrees C, detection limits were reduced for compounds of low hydrophobicity (Kow<501), for example benzene, toluene, 1,1,1-trichloroethane, and trichloroethylene. In the concentration range 0.5-62.5 microg L(-1), the sensitivity of HS-SPME was enhanced by a factor of approximately two for all compounds by performing the extraction at -20 degrees C. A possible explanation is that freezing of the water sample results in higher concentration of the target compounds in the residual liquid phase and gas phase (freezing-out), combined with enhanced adsorption of the compounds by the cooled fiber. The precision of HS-SPME, expressed as the relative standard deviation and the linearity of the regression lines, is increased for more hydrophobic compounds (Kow>501) by simultaneous direct fiber cooling and freezing of analyte solution. Background contamination during analysis is reduced significantly by avoiding the use of organic solvents.

Journal Article↗
PubMed2006

Heterogeneous optochemical VOC sensing layers selected by ESI-mass spectrometry.

Spin-coated films of 29H,31H-tetra-4-(2,4-di-tert-amylphenoxy)phthalocyanine (H(2)Pc) and [kappaP,mu-kappaS-(dppeS)Pt(CH(3))](2)[BF(4)](2) have been used as sensing layers deposited in thin film form for the detection of VOCs. The sensing behaviour of the blend was predicted on the basis of mass spectrometric determinations performed on H(2)Pc/Pt-complex solutions, by monitoring the formation of gas-phase ions at the electrospray interface. The addition of small amounts of acetonitrile produced a [M+41](+) peak whereas the addition of similar amounts of methanol, ethanol and isopropyl alcohol did not give the corresponding [M+ROH](+) species. These results were confirmed by sensing tests. A pure phthalocyanine optosensing element did not show relevant selectivity. Conversely, the heterogeneous sensing layer obtained by spin-coating deposition of a Pt-complex/H(2)Pc blend allowed the sensing of acetonitrile vapours with respect to the above mentioned alcohols.

Biocompatible Materials↗
PubMed2006

Kinetics of photocatalytic VOCs abatement in a standardized reactor.

A standardized micro-pilot scale continuous flow apparatus has been built up, using two types of differential photoreactors, and equipped with a refined control of the working conditions in order to study the photocatalytic degradation as a way to abate VOCs in air. Kinetic measurements have been carried out on trichloroethylene (TCE), methanol and benzene as model pollutants. The absence of diffusional limitation and of reaction product effect on the kinetics have both been demonstrated under our working conditions. The influences of concentration, light flux and temperature on the initial degradation rate have been studied. A simple Langmuir-Hinshelwood kinetic model has been verified for TCE and methanol, whereas benzene degradation was more complex and did not follow this simple mechanism. The determined experimental data aim at being useful in the scaling-up of photocatalytic reactors.

Air Pollutants↗
PubMed2006

Development of a simple, accurate SPME-based method for assay of VOCs in column breakthrough experiments.

Solid-phase microextraction (SPME) with gas chromatography is to be used for assay of effluent liquid samples from soil column experiments associated with VOC fate/transport studies. One goal of the fate/transport studies is to develop accurate, highly reproducible column breakthrough curves for 1,2-cis-dichloroethylene (cis-DCE) and trichloroethylene (TCE) to better understand interactions with selected natural solid phases. For SPME, the influences of the sample equilibration time, extraction temperature and the ratio of volume of sample bottle to that of the liquid sample (V(T)/V(w)) are the critical factors that could influence accuracy and precision of the measured results. Equilibrium between the gas phase and liquid phase was attained after 200 min of equilibration time. The temperature must be carefully controlled due to variation of both the Henry's constant (K(h)) and the fibre/gas phase distribution coefficient (K(fg)). K(h) decreases with decreasing temperature while K(fg) increases. Low V(T)/V(w) yields better sensitivity but results in analyte losses and negative bias of the resultant assay. High V(T)/V(w) ratio yields reduced sensitivity but analyte losses were found to be minimal, leading to better accuracy and reproducibility. A fast SPME method was achieved, 5 min for SPME extraction and 3.10 min for GC analysis. A linear calibration function in the gas phase was developed to analyse the breakthrough curve data, linear between a range of 0.9-236 microgl(-1), and a detection limit lower than 5 microgl(-1).

Chromatography, Gas↗
PubMed2006

Influence of physicochemical treatments on spent palladium based catalyst for catalytic oxidation of VOCs.

To recycle the spent catalyst for the removal of VOCs, the benzene, toluene, and xylene (BTX) complete oxidations were studied over pretreated palladium based spent catalyst in a fixed bed flow reactor system at atmospheric pressure. Two different pretreatment methods with gas (air and hydrogen) and acid aqueous solution (HCl, H(2)SO(4), HNO(3), H(3)PO(4) and CH(3)COOH) were used to investigate the catalytic activity of spent catalyst. The properties of the spent and pretreated Pd based catalyst were characterized by XRD, BET, TEM, ICP, and XPS. The results of light-off curves indicate that the catalytic activity of toluene oxidation for pretreated samples is in the order of hydrogen>air>HNO(3)>CH(3)COOH>H(2)SO(4)>H(3)PO(4)>HCl. In addition, the air and the acid aqueous pretreated catalyst activities were significantly decreased compared to that of the spent (or parent) catalyst. Moreover, hydrogen pretreated (or reduced) catalysts having mainly metallic form show the best performance in removing the toluene vapours compared to other pretreated samples. The reduction temperature made a significant difference in the catalytic performance of the spent catalyst pretreated with hydrogen. XPS results clearly supported that the palladium state of the spent catalysts pretreated at 300 degrees C was shifted more toward metallic form than other reduced catalysts. Furthermore, the results of a long-term test and catalytic activity of aromatic hydrocarbons also supported that the hydrogen pretreated spent catalyst was a good candidate for removing toxic compounds.

Acids↗
PubMed2005

A macrokinetic model for dimensioning of biofilters for VOC and odour treatment.

Biofiltration is a cost-effective and environmentally sustainable technology for the treatment of exhaust gases from a variety of sources. Although the process setup is relative simple, many physical, chemical, and microbiological processes are involved. Microkinetic models attempting to cover all of these processes are often more complex than reliable; on the other hand, many macrokinetic approaches have a tendency to oversimplification. In order to develop a simple and accurate protocol to derive biofilter design criteria from experimental trials, a macrokinetic model based on chemical engineering fundamentals was developed. The model covers first-order kinetics as well as kinetics shifting from first-order at low substrate concentrations to zero-order at elevated concentrations and can be applied to single VOCs and odours as measured by olfactometry.

Bioreactors↗
PubMed2001

Comparison of models for describing measured VOC emissions from wood-based panels under dynamic chamber test condition.

Measured emission factors are the experimental data used to represent emission characteristics of volatile organic compounds (VOCs) from testing materials under dynamic chamber test conditions. A simple empirical model that describes the measured emission factors will be very useful for practical purposes. In this study, a power law model was compared with a widely used first-order exponential decay model in their ability to describe measured emission factors of wood-based panel materials. It was demonstrated that the power law model is a better choice than the first-order model for describing emission characteristics for short-term (less than 100 h) experimental data. The power law model was also more superior in predicting long-term (up to 900 h) emission factors.

Air Pollution, Indoor↗
PubMed2001

A dual-adsorbent preconcentrator for a portable indoor-VOC microsensor system.

The development and testing of a miniature dual-adsorbent preconcentrator for a microsensor-based analytical system designed to determine complex volatile organic chemical (VOC) mixtures encountered in indoor working environments at low part-per-billion levels is described. Candidate adsorbents were screened for thermal-desorption bandwidth and breakthrough volume against 20 volatile organic vapors and subsets thereof as a function of several relevant variables. A glass capillary (1.1 mm i.d.) packed with 3.4 mg of Carbopack X and 1.2 mg of Carboxen 1000 provides sufficient capacity for a 1-L dry-air sample containing all 20 vapors at concentrations of 100 ppb as well as providing a composite half-height peak width of <3 s at a desorption temperature of 300 degrees C and a flow rate of 4 mL/min. Required adsorbent masses increase to 7.0 and 1.5 mg, respectively, for the same mixture at component concentrations of 1 ppm. Vapor breakthrough volumes for the Carbopack X are unaffected by humidity from 0 to 100%RH, but those for the Carboxen 1000 are significantly reduced, requiring an additional 0.9 mg of the latter to avoid premature breakthrough at the 100 ppb level. Good peak shapes, efficient chromatographic separation of preconcentrated sample mixture components, and detection limits in the low-parts-per-billion range using an integrated surface-acoustic-wave (SAW) sensor are achieved. Preconcentrator design and operating parameters are considered in terms of the vapor bed-residence times and breakthrough volumes in the context of the modified Wheeler equation.

Adsorption↗
PubMedDate not supplied

Feasibility study of a compact process for biological treatment of highly soluble VOCs polluted gaseous effluent.

Volatile organic compounds (VOCs), representing a wide range of products mainly generated by industrial activity, are involved in air pollution. This study deals with a new biological treatment process of gaseous effluent combining a gas/liquid contactor called an "aero-ejector" and a membrane bioreactor. Combining these two innovative technologies enables a high elimination efficiency to be reached. We first focus on transfer phenomena characterization in a pilot installation on a laboratory scale, using a gaseous effluent polluted with a low ethanol concentration (7.1 x 10(-3) kg.m(-3)). These experiments demonstrated the good transfer performances since 90% of the ethanol was absorbed in the liquid phase in one step. After this physical characterization, the biological aspect of the system was studied using the yeast Candida utilis as microorganism. During the experiment, no ethanol was measured in the fermentation broth nor in the outlet gas, confirming the efficiency of ethanol elimination by C. utilis. The experimental procedure emerging from the present study strongly validates the suitability of this process for ethanol removal from air.

Absorption↗