The development of low volatile organic compound emission house—a case study

An aim in developing low volatile organic compound (VOCs) emission house is to reduce the level of VOCs in domestic housing. In this study, a case study for the reduction of exposure to VOCs from a newly constructed residential house was presented. Before application, the construction materials used in the house were tested in an environmental chamber and low VOC emission materials were then selected. Design of the house abided by the following principals: maximizing the ventilation rate and avoiding the use of high VOC emission materials in the house. By improved building design and proper construction materials selection, risk of personal exposure to VOCs in the house was significantly reduced. The total VOCs (TVOCs) concentrations measured in the house ranged from non-detectable to 43 μg/m³. These values were much lower than the published values (0.48–31.7 mg/m³) for new houses in Scandinavian countries and in the USA. The low TVOCs concentrations obtained in this study probably resulted from the high ventilation rates and the use of low VOCs emission materials. This study also combined the results with the three traditional ways in improvement of IAQ. The results obtained in this study confirmed that the most effective strategy for controlling IAQ was pollution prevention and the next most important was the design of ventilation rates to handle uncontrollable sources. The effectiveness of aging as a means of indoor pollution control was also reviewed.     

Variations in amounts and potential sources of volatile organic chemicals in new cars

This study examines inter-brand, intra-brand and intra-model variations in volatile organic chemical (VOC) levels inside new cars. The effect of temperature on interior VOC levels was examined using model automobiles with and without the air-conditioning running. Potential sources of VOC were assessed by comparing VOC levels with two interior trims (leather and fabric) and by analyzing VOC emissions from various interior components. Five brands of new car, both domestic and imported, were tested. Twelve targeted VOCs were collected on solid sorbents and analyzed using thermal desorption and GC/FID. VOCs from interior parts and adhesives were identified using solid phase micro-extraction (SPME) coupled with GC/MS. The VOC concentrations varied markedly among brands and within models, and individual VOC levels ranged from below the detection limit (a few mug per cubic meter) to thousands of mug per cubic meter. The intra-model variability (mean, 47%) in the VOC levels was approximately 50% that within each brand (mean, 95%). Although interior trim levels affected VOC levels, the effects differed among brands. Reduction of the cabin temperature reduced most VOC levels, but the impact was not statistically significant. Screening tests for VOCs from interior parts revealed that butylated hydroxytoluene (BHT), a common anti-oxidant, was the most common chemical. Long-chain aliphatic hydrocarbons, particularly C14-C17, were identified in most grease (lubricant) samples, and toluene and xylenes were ubiquitously present in adhesive samples. Process-related compounds, such as plasticizer, were also identified in interior parts. In-cabin VOC levels varied significantly among makes/models and interior trims. Concerned consumers should purchase older new cars from manufacturers since VOC levels inside car cabins normally declines over time. Improved processes or materials with lower VOC emission potential should be used to minimize in-cabin VOC sources for new cars.     

Levels and sources of volatile organic compounds in homes of children with asthma

Many volatile organic compounds (VOCs) are classified as known or possible carcinogens, irritants, and toxicants, and VOC exposure has been associated with the onset and exacerbation of asthma. This study characterizes VOC levels in 126 homes of children with asthma in Detroit, Michigan, USA. The total target VOC concentration ranged from 14 to 2274 μg/m³ (mean = 150 μg/m³; median = 91 μg/m³); 56 VOCs were quantified; and d‐limonene, toluene, p, m‐xylene, and ethyl acetate had the highest concentrations. Based on the potential for adverse health effects, priority VOCs included naphthalene, benzene, 1,4‐dichlorobenzene, isopropylbenzene, ethylbenzene, styrene, chloroform, 1,2‐dichloroethane, tetrachloroethene, and trichloroethylene. Concentrations varied mostly due to between‐residence and seasonal variation. Identified emission sources included cigarette smoking, solvent‐related emissions, renovations, household products, and pesticides. The effect of nearby traffic on indoor VOC levels was not distinguished. While concentrations in the Detroit homes were lower than levels found in other North American studies, many homes had elevated VOC levels, including compounds that are known health hazards. Thus, the identification and control of VOC sources are important and prudent, especially for vulnerable individuals. Actions and policies to reduce VOC exposures, for example, sales restrictions, improved product labeling, and consumer education, are recommended.     

人群散发对高校教室室内TVOC浓度动态影响的实测分析

随机选取南京某高校10间在室人员密集的教室,在其使用期间对室内总挥发性有机化合物(TVOC)和CO₂浓度、温湿度,以及室内人员数量和典型活动状况(如开关门窗)等进行了连续监测和对比分析。研究结果表明:冬、春、夏季测试教室室内TVOC质量浓度分别为(363.1±121.7),(218.4±11.5),(583.3±38.9)μg/m³;室内TVOC浓度变化与CO₂类似,总体呈现先上升后下降的趋势,并与室内人员数量变化呈强正相关性;室内TVOC浓度水平存在季节性差异。室内总源强度的估算结果表明,室内不同样本数量的人群散发强度与室内TVOC浓度变化类似,随着人数变化,呈现出先逐渐增大,然后趋于相对稳定,最后逐渐减小的趋势。     

Measurement of volatile organic compounds in sediments of the Scheldt estuary and the Southern North Sea

The concentrations and distribution of 13 priority volatile organic compounds (VOCs) were determined in sediments of the Scheldt estuary and the Belgian continental shelf, using a modified Tekmar LSC 2000 purge-and-trap system coupled to GC-MS. The method allows a sample intake of up to 50 g wet weight and detection limits are between 0.003 ng/g (tetrachloromethane) and 0.16 ng/g (m- and p-xylene). The repeatability (n = 5) varied between 4% (benzene) and 17% (toluene) and the recoveries ranged from 59% (1,1-dichloroethane) to 99% (tetrachloromethane). Because of the nature of the contaminants, special attention was paid to analyte losses and contamination of the samples during storage aboard the research vessel. Spiked sediment samples were prepared in the laboratory and stored aboard under the same conditions as the environmental samples. The recoveries for these samples varied between 94 and 130%, which suggests that storage had no adverse effect on the samples. No detectable VOC concentrations were found for most of the sampling stations. However, in the Antwerp harbour area, significant concentrations of VOCs were found. The sorption behaviour as predicted from laboratory equilibrium partitioning experiments gives an indication of the in situ partitioning behaviour of VOCs. Although VOCs in sediments should, in general, not be regarded as a major problem in the marine environment, high local concentrations may be a cause of concern.     

Characterization of ozone precursor volatile organic compounds in urban atmospheres and around the petrochemical industry in the Tarragona region

This paper reports the results of an assessment of volatile organic compound (VOCs) levels in ambient air in samples collected at urban and industrial sites in southern Catalonia, which is home to one of the most important petrochemical complexes in southern Europe. This study contains data from a total of 192 samples collected in 2007, from May to October, at six air pollution measurement stations within the area of influence of several chemical and petrochemical industrial plants. The ambient air concentrations of a group of 65 VOCs, some of them ozone precursors, were determined by active sampling into sorbent tubes, thermal desorption and gas chromatography-mass spectrometry. At the same time, several meteorological parameters were also recorded, and levels of NO, NO₂ and O₃ measured by the automatic stations, have been included in the study as well. Ambient air profiles of the different areas were studied, and the ozone formation dependent on VOCs and NO₂ levels was also analysed, taking into account the photochemical ozone creation potential (POCP) for different groups of VOCs.     

Selection between alcohols and volatile fatty acids as external carbon sources for EBPR

The purpose of this paper is to provide a basis for selecting alcohols (i.e. ethanol and methanol) or short-chain volatile fatty acids (VFAs) (i.e. acetate and propionate) as the external carbon sources for enhanced biological phosphorus removal (EBPR) from wastewaters in adapted or unadapted activated sludge. When ethanol is used in an unacclimated process, a period of adaptation is required by polyphosphate-accumulating organisms (PAOs). From 0 to 140 days of ethanol acclimatizing, the P release and uptake rates increased to 6.2 and 7.0 mgP-PO(3)4(-)g(-1)VSSh(-1), respectively. PAOs in ethanol-enriched sludge produced poly-beta-hydroxyvalerate (PHV) (81.9%) as the main polyhydroxyalkanoate (PHA) and reached an effluent phosphate concentration close to zero (0.10 mgP-PO(3)4(-)L(-1)). On the other hand, methanol was not used by PAOs in 30-day ethanol-acclimated sludge in short-term tests. If EBPR needs to be incidentally supported by substrate addition, VFAs are preferred; for long-term addition also ethanol can be considered.     

A study on the relationship between biodegradability enhancement and oxidation of 1,4-dioxane using ozone and hydrogen peroxide

Advanced oxidation involving O₃/H₂O₂ was used to eliminate 1,4-dioxane and to enhance the biodegradability of dioxane-contaminated water. Oxidation experiments were carried out in a bubble column reactor operating in fed-batch. The rate of dioxane removal and enhancement in biodegradability was investigated at hydrogen peroxide to ozone ratios between 0 and 0.6 mol:mol and pH between 5 and 11. A theoretical model was also applied to predict the experimental data and to investigate the effects of dioxane concentration, pH, and H₂O₂ concentration. The model predictions fit the experimental data well and there was a linear correlation between dioxane oxidation and BOD enhancement. At low dioxane concentrations, the oxidation rate was first order and it gradually approached zero order with increasing dioxane concentration. Also, the biodegradability of the solution increased with pH up to about 9 and it stayed constant with further pH increase. Hydrogen peroxide initially enhanced dioxane removal and biodegradability enhancement of the solution. However, at H₂O₂:O₃ ratios greater than about 0.4-0.45 mol:mol, i.e. about 2.90 mM for H₂O₂ concentration, H₂O₂ had negative impacts and resulted in reduced dioxane removal and biodegradability increase.     

The biogenic volatile organic compounds emission inventory in France: application to plant ecosystems in the Berre-Marseilles area (France)

An inventory describing the fluxes of volatile organic compounds (VOCs), isoprene and monoterpenes, and other VOCs (OVOCs) from the biosphere to the atmosphere, has been constructed within the framework of the ESCOMPTE project (fiEld experimentS to COnstrain Models of atmospheric Pollution and Transport of Emissions). The area concerned, located around Berre-Marseilles, is a Mediterranean region frequently subject to high ozone concentrations. The inventory has been developed using a fine scale land use database for the year 1999, forest composition statistics, emission potentials from individual plant species, biomass distribution, temperature and light intensity. The seasonal variations in emission potentials and biomass were also taken into account. Hourly meteorological data for 1999 were calculated from ALADIN data and these were used to predict the hourly isoprene, monoterpene and OVOC fluxes for the area on a 1 kmx1 km spatial grid. Estimates of annual biogenic isoprene, monoterpene and OVOC fluxes for the reference year 1999 were 20.6, 38.9 and 13.3 kt, respectively, Quercus pubescens, Quercus ilex, Pinus halepensis and garrigue vegetation are the dominant emitting species of the area. VOC emissions from vegetation in this region contribute approximately 94% to the NMVOC (non-methane volatile organic compounds) of natural origin and are of the same order of magnitude as NMVOC emissions from anthropogenic sources. These results complete the global ESCOMPTE database needed to make an efficient strategy for tropospheric ozone reduction policy.     

Investigation of volatile organic compounds in office buildings in Bangkok,Thailand: Concentrations,sources, and occupant symptoms

To conserve energy, office buildings with air-conditioning systems in Thailand are operated with a tight thermal envelope. This leads to low fresh-air ventilation rates and is thought to be partly responsible for the sick building syndrome symptoms reported by occupants. The objectives of this study are to measure concentrations and to determine sources of 13 volatile organic compounds (VOCs) in office buildings with air-conditioning systems in the business area of Bangkok. Indoor and outdoor air samples from 17 buildings were collected on Tenax-TA^™ sorbent tubes and analyzed for individual VOCs by thermal desorption-gas chromatography/mass spectrometry (TD–GC/MS). Building ventilation was measured with a constant injection technique using hexafluorobenzene as a tracer gas. The results show that the VOC concentrations varied significantly among the studied buildings. The two most dominant VOCs were toluene and limonene with average concentrations of 110 and 60.5 μg m⁻³, respectively. A Wilcoxon sum rank test indicated that the indoor concentrations of aromatic compounds and limonene were statistically higher than outdoor concentrations at the 0.05 level, while the indoor concentrations of chlorinated compounds were not. Indoor emission factors of toluene and limonene were found to be highest with the average values of 80.9 and 18.9 μg m⁻² h⁻¹, respectively. Principal component analysis was applied to the emission factors of 13 VOCs, producing three components based on source similarities. Furthermore, a questionnaire survey investigation and field measurements of building air exchange pointed to indoor air complaints related to inadequate ventilation.     

Real‐world volatile organic compound emission rates from seated adults and children for use in indoor air studies

Human beings emit many volatile organic compounds (VOCs) of both endogenous (internally produced) and exogenous (external source) origin. Here we present real‐world emission rates of volatile organic compounds from cinema audiences (50‐230 people) as a function of time in multiple screenings of three films. The cinema location and film selection allowed high‐frequency measurement of human‐emitted VOCs within a room flushed at a known rate so that emissions rates could be calculated for both adults and children. Gas‐phase emission rates are analyzed as a function of time of day, variability during the film, and age of viewer. The average emission rates of CO₂, acetone, and isoprene were lower (by a factor of ~1.2‐1.4) for children under twelve compared to adults while for acetaldehyde emission rates were equivalent. Molecules influenced by exogenous sources such as decamethylcyclopentasiloxanes and methanol tended to decrease over the course of day and then rise for late evening screenings. These results represent average emission rates of people under real‐world conditions and can be used in indoor air quality assessments and building design. Averaging over a large number of people generates emission rates that are less susceptible to individual behaviors.     

Characterizing sources and emissions of volatile organic compounds in a northern California residence using space‐ and time‐resolved measurements

We investigate source characteristics and emission dynamics of volatile organic compounds (VOCs) in a single‐family house in California utilizing time‐ and space‐resolved measurements. About 200 VOC signals, corresponding to more than 200 species, were measured during 8 weeks in summer and five in winter. Spatially resolved measurements, along with tracer data, reveal that VOCs in the living space were mainly emitted directly into that space, with minor contributions from the crawlspace, attic, or outdoors. Time‐resolved measurements in the living space exhibited baseline levels far above outdoor levels for most VOCs; many compounds also displayed patterns of intermittent short‐term enhancements (spikes) well above the indoor baseline. Compounds were categorized as “high‐baseline” or “spike‐dominated” based on indoor‐to‐outdoor concentration ratio and indoor mean‐to‐median ratio. Short‐term spikes were associated with occupants and their activities, especially cooking. High‐baseline compounds indicate continuous indoor emissions from building materials and furnishings. Indoor emission rates for high‐baseline species, quantified with 2‐hour resolution, exhibited strong temperature dependence and were affected by air‐change rates. Decomposition of wooden building materials is suggested as a major source for acetic acid, formic acid, and methanol, which together accounted for ~75% of the total continuous indoor emissions of high‐baseline species.     

Non-agricultural sources of groundwater nitrate: a review and case study

Nitrate is often seen as an agricultural pollutant of groundwater and so is expected to be at higher concentrations in the groundwaters surrounding a city than in those beneath it. However the difference between rural and urban nitrate concentrations is often small, due to the non-agricultural sources of nitrogen that are concentrated in cities. This paper illustrates the source and significance of non-agricultural nitrogen for groundwater and presents a case study of nitrate loading in the city of Nottingham. Major sources of nitrogen in urban aquifers are related to wastewater disposal (on-site systems and leaky sewers), solid waste disposal (landfills and waste tips). The major sources of nitrogen in the Nottingham area are mains leakage and contaminated land with approximately 38% each of a total load of 21 kg N ha(-1) year(-1).     

Exploring the relationship between landscape characteristics and urban vibrancy: A case study using morphology and review data

Urban vibrancy is a vital component that supports urban form and is dependent on the physical entities in urban landscapes. Thus, the relationship between urban landscapes and urban vibrancy is a major concern for city planners. While existing studies mainly capture mixed land use, density, and accessibility properties of the physical environment, urban characteristics depicted by the city morphologies have seldom been addressed. To fill this gap, a novel framework is proposed in this paper to explore the relationship between landscape characteristics and urban vibrancy. First, research approaches for delineating multi-level urban landscape characteristics – including places, land use, and single and multiple landscape elements – using spatial metrics were analysed. Then, place-based reviews from social media data were applied as proxies to quantitatively measure urban vibrancy. Finally, regression analyses were proposed to assess the relationship between landscape characteristics and urban vibrancy. Satisfactory regression model performances were attained with adjusted R² values of 0.65, 0.65, 0.66, and 0.67 at each landscape characteristic level. The results indicate that changes in urban vibrancy are variable and highly dependent on the proposed multi-level characteristics. These findings may provide guidance for city planning and urban landscape design.     

外伤性骨折与类风湿性关节炎患病率的关系研究

目的研究外伤性骨折对类风湿性关节炎患病率的影响。方法 2010年12月对甘肃省庆阳地区38~52岁的30名外伤性骨折患者类风湿性关节炎的患病情况进行问卷调查,了解患者在性别、年龄、骨折后感染史及类风湿性关节炎患病率等方面的差异。结果 30名外伤性骨折患者中,有5名在骨折后患上了类风湿性关节炎,其患病率(16.7%)远远高出正常人群(0.3%~1.5%);同时女性发病率(37.5%)也明显高于男性(9.09%)。结论外伤性骨折会使类风湿性关节炎的患病率明显升高。     

Modeling volatile organic compound (VOC) concentrations due to material emissions in a real residential unit. Part I: Methodology and a preliminary case study

High volatile organic compound (VOC) concentrations following building decoration have been observed frequently. In reality, however, residents do not know the indoor VOC concentration levels until the buildings are tested, which seldom provides a preventive measure. While several indoor air quality (IAQ) simulation programs have been developed to predict indoor contaminant levels, case studies in the literature are scarce regarding the predictability of indoor VOC concentrations as well as how such predictions could be performed in real buildings. In this paper, we intended to conduct a proof-of-concept study whether simulations can help to reveal some of the key features of VOC concentrations during indoor decoration process. We conducted a case study, simulated and measured the VOC concentrations of a residential unit during the room decoration process. Results show that while certain agreement was achieved between the measurement and simulation, application of IAQ models to real buildings is challenging under the best of circumstances—single zone spaces with very few emission materials inside.     

Emission factors and characteristics of criteria pollutants and volatile organic compounds (VOCs) in a freeway tunnel study

Carbon monoxide (CO), nitrogen oxide (NO(x)), hydrocarbon (HC), sulfur oxide (SO(2)), particulate matter <10 microm (PM(10)), and 57 VOC species of emissions were confirmed in a freeway tunnel in southern Taiwan. Emission factors were 1.89 (CO), 0.73 (NO(x)), 0.46 (HC), 0.02 (SO2) and 0.06 (PM(10)) g/km-vehicle for all vehicle fleets. Heavy-duty truck and trailer vehicles contributed 20% of the emissions on workdays and 9.5% on weekends in this study. Paraffins and aromatics were the main VOC groups in the tunnel. Isopentane, toluene, n-pentane, isoprene, 2,3-dimethylbutane, acetone, 2-methylpentane, 1-hexene, 1,2,4-trimethybenzene, 1-butene and propene emissions were the major VOC species. Their emission factors were over 10 mg/km-vehicle. Rainfall and high humidity in the tunnel could have reduced the VOC concentrations and increased the portion of aromatics. In addition to paraffins, olefins, and aromatic compounds, oxygenated compounds (i.e., acetone) were found. The pollutant ratios between the inside center and the outside of the tunnel were about 2-3 for CO, SO2, and PM(10) and 42 for NO(x). In addition, the emission factors of the vehicles could reflect real-world vehicle emissions on the highway and be used as baseline information for development of a vehicle control strategy.     

混凝土氯离子扩散性能与时间关系的试验研究

通过设计的考虑单一养护时间因素的试验,用NEL法测定了不同配合比、标准养护时间不同的混凝土的氯离子扩散系数.试验的结果表明,混凝土扩散系数随着养护时间的延长而降低,在混凝土成型250d后扩散系数的降低幅度明显减缓.