Evaluation of low-VOC latex paints

Four commercially available low-volatile organic compound (VOC) latex paints were evaluated as substitutes for conventional latex paints by assessing both their emission characteristics and their performance as coatings. Bulk analysis indicated that the VOC contents of all four paints tested were considerably lower than those of conventional latex paints. Low VOC emissions were confirmed by small chamber emission tests. However, significant emissions of several aldehydes, especially formaldehyde which is a hazardous air pollutant, were detected in emissions from two of the four paints. American Society for Testing and Materials (ASTM) methods were used to evaluate the hiding power, scrub resistance, washability, dry to touch and yellowness index. The results indicated that one of the four low-VOC paints tested showed performance equivalent or superior to that of a conventional latex paint used as control. It was concluded that low-VOC latex paint can be a viable option to replace conventional latex paints for prevention of indoor air pollution. However, paints marketed as "low-VOC" may still have significant emissions of some individual VOCs, and some may not have performance characteristics matching those of conventional latex paints.     

面漆VOCs的散发特性研究

利用自制小型环境箱实验研究了面漆挥发性有机物(VOCs)的散发特性。研究结果表明，气流速率、涂层厚度、基底材料的特性以及基底的边缘效应等对面漆VOCs的散发特性有重要影响。高气流速度可以提高VOCs浓度的衰减速率，缩短面漆VOCs的蒸发时间；涂层越厚，环境箱内VOCs浓度越高，VOCs的蒸发时间越长：采用孔隙率较低的材料作基底，基底内VOCs的残存量低，可减轻建筑物使用后的VOCs低浓度污染。基底“边缘效应”可明显改变VOCs浓度随时间的变化关系。     

Factors controlling volatile organic compounds in dwellings in Melbourne,Australia

This study characterized indoor volatile organic compounds (VOCs) and investigated the effects of the dwelling characteristics, building materials, occupant activities, and environmental conditions on indoor VOC concentrations in 40 dwellings located in Melbourne, Australia, in 2008 and 2009. A total of 97 VOCs were identified. Nine VOCs, n‐butane, 2‐methylbutane, toluene, formaldehyde, acetaldehyde, d‐limonene, ethanol, 2‐propanol, and acetic acid, accounted for 68% of the sum of all VOCs. The median indoor concentrations of all VOCs were greater than those measured outdoors. The occupant density was positively associated with indoor VOC concentrations via occupant activities, including respiration and combustion. Terpenes were associated with the use of household cleaning and laundry products. A petroleum‐like indoor VOC signature of alkanes and aromatics was associated with the proximity of major roads. The indoor VOC concentrations were negatively correlated (P < 0.05) with ventilation. Levels of VOCs in these Australian dwellings were lower than those from previous studies in North America and Europe, probably due to a combination of an ongoing temporal decrease in indoor VOC concentrations and the leakier nature of Australian dwellings.     

TVOC and formaldehyde emission behaviors from flooring materials bonded with environmental-friendly MF/PVAc hybrid resins

Polyvinyl acetate (PVAc) was added as a replacement for melamine-formaldehyde (MF) resin in the formaldehyde-based resin system to reduce formaldehyde and volatile organic compound (VOC) emissions from the adhesives used between plywoods and fancy veneers. A variety of techniques, including 20-l chamber, field and laboratory emission cell (FLEC), VOC analyzer and standard formaldehyde emission test (desiccator method), were used to determine the formaldehyde and VOC emissions from engineered flooring bonded with five different MF resin and PVAc blends at MF/PVAc ratios of 100:0, 70:30, 50:50, 30:70 and 0:100. Although urea-formaldehyde (UF) resin had the highest formaldehyde emission, the emission as determined by desiccator method was reduced by exchanging with MF resin. Furthermore, the formaldehyde emission level was decreased with increasing addition of PVAc as the replacement for MF resin. UF resin in the case of beech was over 5.0 mg/l, which exceeded E2 (1.5-5.0 mg/l) grade. However, MF30:PVAc70 was 相似文献   

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.     

A review of the emission of VOCs from polymeric materials used in buildings

Building and furnishing materials and consumers products are important sources of formaldehyde and other volatile organic compounds (VOCs) in the indoor environment. The emission from materials is usually continuous and may last for many years in a building. The available evidence indicates that VOCs can cause adverse health effects to the building occupants and may contribute to symptoms of ‘Sick Building Syndrome’.

Control of VOC emission should increasingly become an important consideration for the design and manufacture of polymeric materials used in buildings. The EC Construction Products Directive ‘Essential Requirements’ set a framework for limiting the use of materials that could pose a health risk to building occupants. Furthermore, the on-going development of voluntary labelling schemes and data bases of material emissions that could be used by building designers, should further strengthen the demand for ‘low VOC emitting’ products.

This paper reviews available information about the emission of VOCs from polymeric building materials, the level of emissions in the indoor environment and the requirements for testing of the materials.     

Estimating person-to-person variability in VOC emissions from personal care products used during showering

An increasing fraction of volatile organic compounds (VOC) emissions come from the domestic use of solvents, contained within myriad commonplace consumer products. Emission rates are often poorly characterized and depend significantly on individual behavior and specific product formulation and usage. Time-concentration profiles of volatile organic compounds (VOCs) arising from the use of a representative selection of personal care products (PCPs) during showering are generated, and person-to-person variability in emissions calculated. A panel of 18 participants used a standardized set of products, dosages, and application times during showering in a controlled indoor bathroom setting. Proton transfer mass spectrometry was used to measure the in-room VOC evolution of limonene (representing the sum of monoterpenes), benzyl alcohol, and ethanol. The release of VOCs had reproducible patterns between users, but noticeable variations in absolute peak concentrations, despite identical amounts of material being used. The amounts of VOC emitted to air for one showering activity were as follows: limonene (1.77 mg ± 42%), benzyl alcohol (1.07 mg ± 41%), and ethanol (0.33 mg ± 78%). Real-world emissions to air were between 1.3 and 11 times lower than bottom-up estimates based on dynamic headspace measurements of product emissions rates, likely a result of PCPs being washed away before VOC evaporation could occur.     

Long-term Emission of Volatile Organic Compounds from Waterborne Paints – Methods of Comparison

The emission of volatile organic compounds (VOCs) from five different waterborne paints was measured in small climatic chambers under standard conditions over a one-year period. The aims of the study were to evaluate the time emission profiles and to develop methods for comparison of different paints. The paints were applied to tin-plated steel sheets. VOCs were sampled on Tenax TA and analysed by thermal desorption and gas chromatography. The chamber concentrations increased rapidly during the first few hours and then decreased as the emission rates dropped. A model expression including an exponentially decreasing emission rate of the paint film, the air exchange rate, and a normalization of the film thickness was fitted to the concentration versus time data. The time required to reach a given emission rate was estimated and found suitable for comparison of the emission of VOCs from the paints. It was found that data sampled within three weeks or less may be sufficient to predict the emission of VOCs up to one year. Reduction of long-term emissions may be achieved most efficiently by (1) substituting a more -volatile VOC whose emission is controlled by evaporation for a less volatile VOC characterized by diffusion-controlled emission and (2) reducing the paint film thickness rather than reducing the initial VOC content of the paint.     

UV-PCO device for indoor VOCs removal: Investigation on multiple compounds effect

Current design models for ultraviolet photocatalytic oxidation (UV-PCO) devices often assume that the air contains only one volatile organic compound (VOC) species or all the VOCs in the air can be treated on a non-interacting basis. However, trace-level multiple VOCs co-exist in most indoor environments. This paper assesses the significance of interference effects among different VOCs for indoor applications by full-scale “pull-down” experiments assisted with model simulations. Multiple versus single VOC tests were performed on selected groups of compounds under low concentration levels. Removal efficiency for each compound was calculated. It was found that the interference effect among test VOCs were generally small in the 2-VOC and 3-VOC mixture tests performed on toluene, ethylbenzene, octane, decane and dodecane with initial concentration of approximate 1 mg/m³ for each compound. However, in the 16 VOC mixture test, the interference effect among different VOCs became quite obvious, and compounds with lower removal efficiency in the single compound test appeared to also have relatively lower efficiency and more obvious delay period in the initial reaction. The L–H model appears to be able to account for this effect if reaction rate constants can be accurately estimated. Results, although limited, indicate that interference between multiple VOCs may not be neglected for the PCO reactor for indoor applications where the number of VOCs species is large and the TVOC concentration is high.     

Emissions of VOCs,SVOCs, and mold during the construction process: Contribution to indoor air quality and future occupants’ exposure

Building materials and human activities are important sources of contamination indoors, but little information is available regarding contamination during construction process which could persist during the whole life of buildings. In this study, six construction stages on two construction sites were investigated regarding the emissions of 43 volatile organic compounds (VOCs), 46 semi-volatile organic compounds (SVOCs), and the presence of 4 genera of mold. Results show that the future indoor air quality does not only depend on the emissions of each building product but that it is also closely related to the whole implementation process. Mold spore measurements can reach 1400 CFU/m³, which is particularly high compared with the concentrations usually measured in indoor environments. Relatively low concentrations of VOCs were observed, in relation to the use of low emissive materials. Among SVOCs analyzed, some phthalates, permethrin, and hydrocarbons were found in significant concentrations upon the delivery of building as well as triclosan, suspected to be endocrine disruptor, and yet prohibited in the treatment of materials and construction since 2014. As some regulations exist for VOC emissions, it is necessary to implement them for SVOCs due to their toxicity.     

Volatile organic pollutants in new and established buildings in Melbourne, Australia

Volatile organic compounds (VOCs) within new and established buildings have been determined and factors significant to their presence have been identified. In established dwellings, total volatile organic compound (TVOC) concentrations were low, but were approximately four times higher than in outdoor air, showing a dominant effect of indoor sources. The presence of attached garages, site contamination and 'faulty' wool carpet were associated with higher indoor pollution. In three dwellings, unidentified sources of benzene were indicated. Much higher VOC concentrations were observed in new or renovated buildings, persisting above "baseline" levels for several weeks, concentration decay rate correlating with VOC molecular volume, indicating emissions were limited by material diffusion processes. VOC and formaldehyde emission decays in a new dwelling occurred by a double-exponential source model. This shows that persistent low levels of volatile organic pollutants in established dwellings can occur due to long-term emissions from building materials.     

Concentrations of Volatile Organic Compounds in Indoor Air – A Review

A review is presented of investigations of volatile organic compound (VOC) concentrations in indoor air of buildings of different classifications (dwellings, offices, schools, hospitals) and categories (established, new and complaint buildings). Measured concentrations obtained from the published literature and from research in progress overseas were pooled so that VOC concentration profiles could be derived for each building classification/category. Mean concentrations of individual compounds in established buildings were found to be generally below 50 μg/m³, with most below 5 μg/m³. Concentrations in new buildings were much greater, often by an order of magnitude or more, and appeared to arise from construction materials and building contents. The nature of these sources and approaches to reduce indoor air concentrations by limiting source VOC emissions is discussed. Total VOC (TVOC) concentrations were substantially higher than concentrations of any individual VOCs in all situations, reflecting the large number of compounds present, but interpretation of such measurements was limited by the lack of a common definition for TVOC relevant to occupant exposure.     

Source apportionment of volatile organic compounds in Hong Kong homes

Indoor volatile organic compound (VOC) data obtained in 100 Hong Kong homes were analyzed to investigate the nature of emission sources and their contributions to indoor concentrations. A principal component analysis (PCA) showed that off-gassing of building materials, household products, painted wood products, room freshener, mothballs and consumer products were the major sources of VOCs in Hong Kong homes. The source apportionments were then evaluated by using an absolute principal component scores (APCS) technique combined with multiple linear regressions. The results indicated that 76.5 ± 1% (average ± standard error) of the total VOC emissions in Hong Kong homes attributes to the off-gassing of building materials, followed by the room freshener (8 ± 4%), household products (6 ± 2%), mothballs (5 ± 3%) and painted wood products (4 ± 2%). Analysis on the source strength in the monitored homes revealed that although six indoor sources were identified and quantified in the Hong Kong homes, only some homes were responsible for the elevated concentrations of target VOCs emitted from these sources. The findings provide us the mechanism of reducing levels of indoor VOCs and ultimately lead to cost effective reduction in population exposures.     

Substrate effects on VOC emissions from an interior finishing varnish

The effects of four substrates—an aluminium board, a plasterboard, a gypsum board and a plywood board—on volatile organic compound (VOC) emissions from an interior finishing varnish were investigated using a dynamic environmental chamber. Four major VOCs, including toluene, ethylbenzene, m,p-xylene and o-xylene, were identified in the varnish emissions. The average amount of VOCs emitted from the painted aluminium substrate was approximately 65% more than that from the painted plywood substrate during the $\text{10}\text{h}$ test period. The results indicated that most VOC emissions from the painted aluminium substrate occurred in the early stage through an evaporation-like processes. However, the majority of the VOC from the plywood substrate was emitted in a later stage through a diffusion-like process. The present work confirmed that the type of substrates had a marked influence on the VOC emissions resulting from varnish.     

Ozone reaction with clothing and its initiated VOC emissions in an environmental chamber

Human health is adversely affected by ozone and the volatile organic compounds (VOCs) produced from its reactions in the indoor environment. Hence, it is important to characterize the ozone‐initiated reactive chemistry under indoor conditions and study the influence of different factors on these reactions. This investigation studied the ozone reactions with clothing through a series of experiments conducted in an environmental chamber under various conditions. The study found that the ozone reactions with a soiled (human‐worn) T‐shirt consumed ozone and generated VOCs. The ozone removal rate and deposition velocity for the T‐shirt increased with the increasing soiling level and air change rate, decreased at high ozone concentrations, and were relatively unaffected by the humidity. The deposition velocity for the soiled T‐shirt ranged from 0.15 to 0.29 cm/s. The ozone‐initiated VOC emissions included C6–C10 straight‐chain saturated aldehydes, acetone, and 4‐OPA (4‐oxopentanal). The VOC emissions were generally higher at higher ozone, humidity, soiling of T‐shirt, and air change rate. The total molar yield was approximately 0.5 in most cases, which means that for every two moles of ozone removed by the T‐shirt surface, one mole of VOCs was produced.     

The effect of temperature on the emission of formaldehyde and volatile organic compounds (VOCs) from laminate flooring — case study

The effect of temperatures of 23, 29, 50°C on formaldehyde and volatile organic compounds (VOCs) emission from laminate flooring Type A (with particleboard as substrate) and Type B (with high density fibre (HDF)) was examined. At 23 and 29°C the measurements did not show any emissions of formaldehyde and very low emissions of VOCs. At a temperature of 50°C, Type A showed a high initial emission of formaldehyde and VOCs, which decreased with time. The emission from Type B was much lower. In conclusion, some laminate flooring may affect the chemical contamination of indoor air with the use of floor heating.     

Contribution of human‐related sources to indoor volatile organic compounds in a university classroom

Although significant progress has been made in understanding the sources and chemistry of indoor volatile organic compounds (VOCs) during the past decades, much is unknown about the role of humans in indoor air chemistry. In the spring of 2014, we conducted continuous measurements of VOCs using a proton transfer reaction mass spectrometer (PTR‐MS) in a university classroom. Positive matrix factorization (PMF) of the measured VOCs revealed a ‘human influence’ component, which likely represented VOCs produced from human breath and ozonolysis of human skin lipids. The concentration of the human influence component increased with the number of occupants and decreased with ventilation rate in a similar way to CO₂, with an average contribution of 40% to the measured daytime VOC concentration. In addition, the human skin lipid ozonolysis products were observed to correlate with CO₂ and anticorrelate with O₃, suggesting that reactions on human surfaces may be important sources of indoor VOCs and sinks for indoor O₃. Our study suggests that humans can substantially affect VOC composition and oxidative capacity in indoor environments.     

确定建筑材料有害物散发量的三种传质模型

室内空气污染源散发量的确定是建立室内空气质量(IAQ)模型的重要步骤之一。目前研究建筑装饰材料和建筑涂料散发污染物的模型主要有经验模型和理论模型两类。经验模型简洁，但应用受到测试条件的限制，不具有普适性。基于传质理论而提出的理论模型目前研究较多，本文对研究建筑材料散发有害物的三个传质模型进行了评述。VB模型是一个简单的溶剂基室内涂料散发的总挥发性有机物(TVOC)的传质模型，低估了污染物的长期散发量。对流传质模型是基于界面平衡所导出的稳态模型，适用于固体和液体等材料的散发过程。Yang等提出的四层传质模型通常需与数值求解结合，计算较麻烦，但能较好地确定建筑材料散发挥发性有机物的散发量。     

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.