Comparison of VOC and ammonia emissions from individual PVC materials, adhesives and from complete structures

Emission rates of volatile organic compounds (VOCs) and ammonia measured from six PVC materials and four adhesives in the laboratory were compared to the emission rates measured on site from complete structures. Significantly higher specific emission rates (SERs) were generally measured from the complete structures than from individual materials. There were large differences between different PVC materials in their permeability for VOCs originating from the underlying structure. Glycol ethers and esters from adhesives used in the installation contributed to the emissions from the PVC covered structure. Emissions of 2-ethylhexanol and TXIB (2,2,4-trimethyl-1,3-pentanediol diisobutyrate) were common. High ammonia SERs were measured from single adhesives but their contribution to the emissions from the complete structure did not appear as obvious as for VOCs. The results indicate that three factors affected the VOC emissions from the PVC flooring on a structure: 1) the permeability of the PVC product for VOCs, 2) the VOC emission from the adhesive used, and 3) the VOC emission from the backside of the PVC product.     

Screening of household products for the emission of volatile organic compounds

10 household products, eight waxes or polishes, and two detergents have been screened by a headspace technique for the emission of volatile organic compounds (VOC). Using Tenax sampling and analysis by combined gas chromatography-mass spectrometry (GC-MS) more than 80 single compounds or groups of isomers have been identified, and semiquantitative data on the initial emission rates (emission rate immediately after application) have been obtained. Products fall into two groups: those containing water as a main (80 to 90%) constituent and those without water. The initial emission rate of the first group ranged from 0.2 to 2 μg cm⁻²min⁻¹, whereas the second group had higher emission rates of up to 430 μg cm⁻²min⁻¹. Products of the second group emit essentially hydrocarbons (alkanes, alkenes, and terpenes), whereas most products of the first group emit oxygenated compounds including terpene alcohols and their acetates, aliphatic alcohols and esters, and alkoxy-alcohols.     

Human impacts on methane emission from mangrove ecosystems in India

This study deals with the emission of methane in relation to changing environmental conditions and human impact, in three mangrove ecosystems of south India. Time-varying fluxes of methane adopting the close chamber technique were used to estimate CH₄ emission from an unpolluted site (Pichavaram mangroves) and two polluted sites viz. (1) Ennore Creek mangroves (affected by fertilizer effluents and crude oil discharges) and (2) Adyar estuary mangroves (affected by the discharges of organic and industrial wastes), covering monthly and seasonal variations. The results indicate annual average CH₄ emissions of 7.4, 5.02 and 15.4 mg m⁻² h⁻¹ from the sediment–water interface of the Pichavaram, Ennore Creek and Adyar estuary respectively. Emission characteristics obtained at Pichavaram mangroves represent a natural variability with changing physico-chemical factors, whereas the emission characteristics at Ennore Creek and Adyar estuary mangroves show anthropogenic influence. Several environmental factors such as oxygen availability, organic matter, soil physical and chemical properties, in addition to human-mediated interventions have been identified as influencing emission rates in the mangrove ecosystems. Preliminary CH₄ emission estimates for the mangrove ecosystems along the Indian sub- continent and the tropical and subtropical coastline of the world by linear extrapolation based on surface area range from 0.05 to 0.37 and 2.8 to 19.25 Tg CH₄ year⁻¹ respectively. Our results also highlight the impact of human activities on future emission of methane from the mangrove ecosystems. Received: 3 March 1999 / Accepted: 14 September 1999     

Emission modelling and validation of VOCs' source strengths in air-conditioned office premises

An emission model for indoor volatile organic compounds (VOCs) based on mass balance considerations has been presented and validated under steady state conditions. Comparison were made for the measured and predicted concentrations of 37 selected VOCs and TVOC through a case intervention study on the filters of the ventilation system in a new commercial air-conditioned office building. The intervention involved replacing media filters with electronic and carbon filtration. TVOC and 37 compounds selected for their health and comfort impact, representation of major chemical classes that occur in indoor air and their utility as markers of pollution sources were studied. The concentration levels predicted by the model were compared with actual measurements. Twenty-five target compounds and the TVOC were adequately described by the model where the measured concentrations were in agreement with the predicted concentrations. Modeling of the remaining 12 compounds was found to be affected by the emission rates that were occupant related.     

A review of airborne polycyclic aromatic hydrocarbons (PAHs) and their human health effects

Polycyclic aromatic hydrocarbons (PAHs) are a large group of organic compounds comprised of two or more fused benzene rings arranged in various configurations. PAHs are widespread environmental contaminants formed as a result of incomplete combustion of organic materials such as fossil fuels. The occurrence of PAHs in ambient air is an increasing concern because of their carcinogenicity and mutagenicity. Although emissions and allowable concentrations of PAHs in air are now regulated, the health risk posed by PAH exposure suggests a continuing need for their control through air quality management. In light of the environmental significance of PAH exposure, this review offers an overview of PAH properties, fates, transformations, human exposure, and health effects (acute and chronic) associated with their emission to the atmosphere. Biomarkers of PAH exposure and their significance are also discussed.     

A review of the significance and formation of chlorinated N-organic compounds in water supplies including preliminary studies on the chlorination of alanine,tryptophan, tyrosine,cytosine, and syringic acid

Nitrogenous organic compounds are of environmental significance because of their potential as both trihalomethane (THM) and nonpurgeable organic halide (NPOX) precursors. They additionally lead to falsely positive tests for free available chlorine (FAC) and are components in the reaction of chlorine to form dihaloacetonitriles (DHANs). A large number of naturally occurring nitrogenous compounds additionally react readily with aqueous chlorine exerting significant chlorine demand. Such reactions generally involve the substitution of chlorine for hydrogen on a nitrogen atom. Additionally, N-chloroorganic materials may be produced even when the precursor concentration is low owing to the rapid specific rate of formation. While previous attention has been largely focused on nonpolar chlorinated organic contaminants such as THMs, the wide distribution of N-organic compounds in water, as well as their general reactivity towards aqueous chlorine, warrant further attention and study to this group of materials. Preliminary studies on the chlorination of several N-organic compounds at a few chlorine-to-compound molar ratios at pH 7 and 4.7 over several reaction intervals are presented. NPOX formation was quite rapid and comprised the greatest proportion of the total organic halide formed for the conditions studied.     

Indoor air pollution due to organic gases and vapours of solvents in building materials

The emission of organic gases and vapours of solvent type from 42 commonly used building materials was measured under standard atmospheric conditions. An average of 22 compounds was found in the air around each building material, and the total concentration of gases and vapours was from 0.01 to 1410 mg/m³. The average arithmetic emission rate was 9.5 mg/m² h, and 52 different compounds were identified. A mathematical model was established for the indoor air concentrations of pollutants originating from building materials. The model was tested on three model rooms constructed from the materials investigated. The calculated total air concentrations of gases and vapours in the three rooms ranged from 1.6 to 23.6 mg/m³, and the number of compounds in the air from 23 to 32. These concentrations and number of compounds did not differ from those found in actual rooms similar in size and construction to the model rooms. The risks of health effects due to the compounds identified from the building materials were investigated, and criteria for future air quality standards are discussed. It is concluded that the possibility of negative health effects cannot be neglected, especially not for the more sensitive minority of the general population.     

Human exposure to PCDD/Fs in the UK: the development of a modelling approach to give historical and future perspectives

In order to assess the long-term impact of persistent organic contaminants such as polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) it is important to be able to quantify historical exposure. An understanding of past exposure is not only important to place our current body burdens in perspective, but is useful in assessing our potential future exposure. Unfortunately, very few direct measurements of our main source of exposure (i.e., food) over the past decades are available. This study attempts to reconstruct the historical exposure of the UK population to PCDD/Fs using a combination of emission estimates, information on environmental temporal trends derived from sediment cores and archived materials, and environmental/human fate modelling. Predicted adipose and blood lipid concentrations for a typical cross section of the population are derived over time (1920-2000), which is compared with measured data. The approach has been tested with two PCDDs and two PCDFs and showed encouraging agreement with measured data. Certain parts of the modelling methodology have been highlighted where there is still poor understanding of the processes governing fate and behaviour. These areas are discussed and recommendations for future improvements are made. The paper thus represents an initial modelling approach which defines both the historical (1920-present) and future (present-2020) fate of PCDD/Fs in the UK population.     

Determination of potentially bioaccumulating complex mixtures of organochlorine compounds in wastewater: a review

Organic chlorine compounds can be persistent environmental contaminants and may be accumulated through the food chain to the aquatic organisms, to fish and humans, depending basically on their hydrophobic properties. Consequently, there is an interest to measure these organic compounds from both the scientific and regulatory communities. The analytical essays have been improved for measuring specific organic chlorine compounds that present the most toxicological potential (polychlorinated biphenyls [PCBs], certain pesticides and dioxins), although they are tedious and time-consuming procedures. The existing tests to measure adsorbable organic halogens (AOX) or extractable organic halogens (EOX) do not distinguish the more hydrophobic organic chlorine matter. The intention of this paper is to make a review of the existing methods to measure the potentially bioaccumulating organochlorine compounds (OCs) from wastewater and propose a methodology to a standardisation procedure for complex mixtures of OCs in wastewater, such as pulp mill effluents. A new method has been proposed for determining the most hydrophobic part of the extractable organic halogens (EOX(fob)), the lowest reported value is 0.6 microg/l, expressed as chloride, and the relative standard deviation at 20 microg/l is 7% on laboratory samples and 30% on real effluents. This new procedure could be a valuable tool to complement environmental risk assessment studies of wastewater discharges.     

Polar organic pollutants in air: A review of collection and analysis

Pollutants which are capable of being extracted into nonpolar solvent such as hexane have received the greatest attention in environmental monitoring. However, the polar fraction, inherently more difficult to analyze, is currently undergoing closer scrutiny. Sampling methods specifically designed to entrap polar particles and vapors are compared. Ion-exchange and reversed-phase liquid chromatography columns are examples of such specific sampling techniques. Various extraction schemes are presented with their individual problems and capabilities. Although there are numerous papers on the analysis of polar organic pollutants, few report actual measurements of ambient air samples. Current reports on polar organic pollutants measured in air samples are summarized. Polar organics are generally divided into three categories: acidic, basic, and neutral. Analytical methods relating to the following categories of polar organic compounds are reviewed: (1) phenols, mono- and dicarboxylic acids, and sulfonic acids, (2) aliphatic and aromatic amines, and (3) alcohols, aldehydes and ketones, phthalate esters, isocyanates and N-nitrosamines. Derivatization techniques, such as ester formation, are compared to the analysis of the unsubstituted compound. The formation of such derivatives is often the best way to trace specific compounds at very low levels.     

Validation of the new passive monitor without a membrane in indoor air

A series of experiments were conducted to investigate the suitability of activated carbon cloth (ACC) strips for diffusive sampling of volatile organic compounds in air without using a membrane. Experiments were carried out in an environmental chamber and in an indoor air environment. The monitors were analyzed qualitatively by liquid extraction and gas chromatography-mass spectrometry and quantitatively by gas chromatography with a flame ionization detector. It was shown that ACC monitors can provide satisfactory quantitative data for a wide variety of volatile organic compounds in indoor air ranging in concentration from 1 mg/m³ to 0.02 g/m³. It was also observed that the absence of a membrane does not affect the linearity of the sampling rate. In addition, a packaging system has been developed that allows samples to be sent out and returned to the laboratory for analysis by mail. Recycling, a convenient procedure of exposure, delivery, and return by postal service, as well as simple analysis all show that this passive sampler substantially reduces the cost of monitoring, thus demonstrating its benefits in the determination of contamination sources within both large industrial sites or any other building where such an analysis may be required.     

Setting up the criteria and credit-awarding scheme for building interior material selection to achieve better indoor air quality

Methods, standards, and regulations that are aimed to reduce indoor air pollution from building materials are critically reviewed. These are classified as content control and emission control. Methods and standards can be found in both of these two classes. In the regulation domain, only content control is enforced in some countries and some regions, and asbestos is the only building material that is banned for building use. The controlled pollutants include heavy metals, radon, formaldehyde, and volatile organic compounds (VOCs). Emission rate control based upon environment chamber testing is very much in the nature of voluntary product labeling and ranking, and this mainly targets formaldehyde and VOC emissions. It is suggested that radon emission from building materials should be subject to similar emission rate control. A comprehensive set criteria and credit-awarding scheme that encourages the use of low-emission building material is synthesized, and how this scheme can be practiced in building design is proposed and discussed.     

Life cycle energy and CO2 emissions analysis of food packaging: an insight into the methodology from an Italian perspective

Packaging is strictly connected to environmental issues as it is a product characterised by high material consumption rate; it is often transported over long distances and has a short life. Providing environmental analysis is, therefore, urgent to identify energy and resources efficient solutions. The paper, taking advantage of a real case study, presents a life cycle-based comparative analysis among three different food packaging systems. The paper compares the life cycle of tin steel, polypropylene and glass-based packaging of an Italian preserves producer. The analysis leads to the conclusion that, for the baseline scenario, polypropylene packaging represents the greenest solution, whereas glass packaging is the worst choice. The paper presents a scenario analysis varying both the method used for accounting for recycling as well as the recycling rates of the packaging materials. Changes in overall results with parameters analysis changing are calculated and highlighted throughout the paper. The impact of a reuse policy of the glass-based solution is also analysed; a model for disposable glass packaging is proposed and the obtained results are compared with the single use polypropylene and tin steel-based packaging. In order to analyse the impact of different End of Life scenarios on the present case study, collecting as well as recycling rates of some European countries have been used. The results revealed a significant fluctuation both in energy consumption and in CO₂ emission as the nation changes. Summing up, a methodology for packaging environmental impact analysis is applied to a real case study, some crucial aspects of the methodology have been analysed in depth in order to give a contribution in packaging environmental impact analysis.     

An overview of commercially used brominated flame retardants,their applications,their use patterns in different countries/regions and possible modes of release

Brominated flame retardants (BFRs) are used in a variety of consumer products and several of those are produced in large quantities. These compounds have been detected in environmental samples, which can be attributed to the anthropogenic uses of these compounds. Brominated flame retardants are produced via direct bromination of organic molecules or via addition of bromine to alkenes; hence, an overview of the production and usage of bromine over the past three decades is covered. Production, application, and environmental occurrence of high production brominated flame retardants including Tetrabromobisphenol A, polybrominated biphenyls, Penta-, Octa-, Deca-brominated diphenyl ether (oxide) formulation and hexabromocyclododecane are discussed.     

The determination of γ-ray absorbed dose rates in air above igneous and sedimentary rocks on SW dartmoor

Calculations have been made to determine the γ-ray absorbed dose rate in air above different types of rock using a single group radiation attenuation model. The results obtained are then compared with dose rates measured with a compensated environmental Geiger-Muller counter. The measurements were made above granite, slate, and dolerite and also on alluvium overlying granite. The comparison shows good agreement between measured and calculated dose rates taking into account the limitations inherent in both the calculations and measurements.     

Effect of mixing chamber venturi,injection timing,compression ratio and EGR on the performance of dual-fuel engine operated with HOME and CNG

Stringent environmental policies and the ever increasing demand for energy have triggered interest in novel combustion technologies that use alternative fuels as energy sources. Of these, pilot-ignited compressed natural gas (CNG) engines that employ small biodiesel pilot to ignite a premixed natural gas–air mixture have received considerable attention. This paper discusses the effect of mixing chamber venturi, injection timing, compression ratio and exhaust gas recirculation (EGR) on the performance of dual-fuel engine operated on biodiesel derived from honge oil and is called honge oil methyl ester (HOME) and CNG. The proposed study mainly focuses on the manifold induction of CNG along with HOME injection. However, CNG can also be injected using port or direct gas injector (Lakshmanan and Nagarajan 2010, Energy 35, pp. 3172–3178). The future study will involve these methods of CNG injection. From this study, it is concluded that an advanced injection timing and an increased compression ratio resulted in increased brake thermal efficiency and reduced smoke, hydrocarbons and carbon monoxide emissions. However, nitrogen oxides (NO _x ) emission increased significantly. The increased NO _x emission was effectively reduced with EGR method. A mixing chamber venturi of 3 mm size, injection timing of 27° before top dead centre (BTDC), compression ratio of 17.5 and 10% EGR were found to be optimum for the modified compression ignition engine that was operated on CNG–HOME dual-fuel mode.     

A first European scale multimedia fate modelling of BDE-209 from 1970 to 2020

The European Variant Berkeley Trent (EVn-BETR) multimedia fugacity model is used to test the validity of previously derived emission estimates and predict environmental concentrations of the main decabromodiphenyl ether congener, BDE-209. The results are presented here and compared with measured environmental data from the literature. Future multimedia concentration trends are predicted using three emission scenarios (Low, Realistic and High) in the dynamic unsteady state mode covering the period 1970–2020. The spatial and temporal distributions of emissions are evaluated. It is predicted that BDE-209 atmospheric concentrations peaked in 2004 and will decline to negligible levels by 2025. Freshwater concentrations should have peaked in 2011, one year after the emissions peak with sediment concentrations peaking in 2013. Predicted atmospheric concentrations are in good agreement with measured data for the Realistic (best estimate of emissions) and High (worst case scenario) emission scenarios. The Low emission scenario consistently underestimates measured data. The German unilateral ban on the use of DecaBDE in the textile industry is simulated in an additional scenario, the effects of which are mainly observed within Germany with only a small effect on the surrounding areas. Overall, the EVn-BTER model predicts atmospheric concentrations reasonably well, within a factor of 5 and 1.2 for the Realistic and High emission scenarios respectively, providing partial validation for the original emission estimate. Total mean MEC:PEC shows the High emission scenario predicts the best fit between air, freshwater and sediment data. An alternative spatial distribution of emissions is tested, based on higher consumption in EBFRIP member states, resulting in improved agreement between MECs and PECs in comparison with the Uniform spatial distribution based on population density. Despite good agreement between modelled and measured point data, more long-term monitoring datasets are needed to compare predicted trends in concentration to determine the rate of change of POPs within the environment.     

The influence of ventilation on indoor/outdoor air contaminants in an office building

The air quality in a newly built preschool was investigated in a longitudinal study. Typical air contaminants emanating from building materials were determined, their variation over time (0–18 months) was measured, and the influence of the ventilation system (81%–91% recirculation of return air) on contaminant concentrations was studied. Volatile organic compounds were sampled by adsorption on porous polymer, analysed by a GC/FID system, and identified by MS. A spatial build-up in concentration (ppb or μg/m³ levels) is evident for all the organic compounds, as well as for CO₂, from the outdoor air, through the ventilation system, and through the rooms to the exhaust air. The longitudinal comparison over time shows that all the organic compounds decline in concentration mainly within the first 6 months of occupancy: 1-butanol 4–14 times, toluene and pentanal + hexanal 2–4 times, while formaldehyde remained at a constant low level of 90 ppb (110 μg/m³). It is difficult to believe that the problems of poor air quality in 100 preschools in Stockholm are caused by the organic compounds alone unless interactions occur. A preschool building needs to be gassed off during the first 6 months after its construction with no recirculation of return air allowed (outdoor air rate approx 4–5 ach). During at least 1–2 additional years, it is desired that the recirculation rate of return air is restricted, perhaps to 50%.     

Removal of trace organic contaminants from domestic wastewater: A meta-analysis comparison of sewage treatment technologies

Trace organic contaminants (TrOCs), such as endocrine disrupting compounds (EDCs) and pharmaceuticals and personal care products (PPCPs), represent global threats to aquatic animals and ecosystems. A major source of TrOCs in the aquatic environment is via the discharge of treated sewage, so there is an urgent need to evaluate the comparative efficiencies of the most widely used sewage treatment technologies as regards elimination of these compounds from wastewater. To address this need, 976 published articles were compiled focusing on estimates of removal (%) for 20 common environmental TrOCs, from five major sewage treatment technologies: conventional activated sludge (CAS), oxidation ditch (OD), membrane bioreactor (MBR), ponds and constructed wetlands (PCW), and trickling biological filters (TBF). A quantitative meta-analysis was performed to compare standardized relative removal efficiencies (SREs) of the compounds amongst these technologies, and where possible potential sources of heterogeneity were considered (e.g., flow rates and chemical sorption potential). The results indicate that the most widely used CAS treatment and the less common TBF provide comparatively poor overall removal of common organic micropollutants. Membrane bioreactors appear to be capable of achieving the greatest overall removal efficiencies, but the sustainability and economic viability of this option has been questioned. Treatment with OD systems may be more economical while still achieving comparatively high removal efficiencies, and the analysis revealed OD to be the best option for targeting highly potent estrogenic EDCs. This study offers a unique global assessment of TrOC removal via leading sewage treatment technologies, and is an important step in the identification of effective options for treating municipal sewage.     

Pollutant emission rates from indoor combustion appliances and sidestream cigarette smoke

Particulate and gaseous emissions from indoor combustion appliances and smoking can elevate the indoor concentrations of various pollutants. Indoor pollutant concentrations resulting from operating one of several combustion appliances, or from sidestream tobacco smoke, were measured in a 27-m³ environmental chamber under varying ventilation rates. The combustion appliances investigated were gas-fired cooking stoves, unvented kerosene-fired space heaters, and unvented natural-gas-fired space heaters. Results showed elevated levels of carbon dioxide, carbon monoxide, nitric oxide, nitrogen dioxide, formaldehyde, and suspended particles from one or more of the pollutant sources investigated. Our findings suggest that, of the sources examined in this study, nitrogen dioxide from combustion appliances and particles from sidestream cigarette smoke are the most serious contaminants of indoor air, if we use existing standards and guidelines as the criteria. An emission rate model was used to quantify the strengths of the pollutant sources, which are reported in terms of the mass of pollutant emitted per energy unit of fuel consumed (in the case of gas and kerosene appliances) and per mass of tobacco combusted (in the case of smoking).