Source apportionment and ozone formation potential of volatile organic compounds in Lagos (Nigeria)

Concentrations of volatile organic compounds (VOCs) of the city air in Oba Akran road, Lagos were investigated. The chlorinated VOCs and xylene in Oba Akran were high. The average benzene/toluene ratio in Oba Akran was 1.7 suggesting that vehicular emission was a possible VOC source in most areas of Oba Akran. The toluene/(m+p-xylene) ratio also suggests a common source of toluene and xylene at these sites, presumably organic solvent used by industries located at Oba Akran. Our results showed that 7.10 tons of CO ₂ equivalents of VOCs are being emitted per year from Oba Akran. Xylenes were found to be the largest contributor to the ozone formation followed by trichloroethylene. A multivariate statistical analysis (Factor analysis extracted with Principal Component Analysis) has been applied to a set of data, and it was found that the main principal components, extracted from the air VOC pollution data, were related to gasoline and oil combustion/industrial activities.     

Photolysis and photooxidation of typical gaseous VOCs by UV Irradiation: Removal performance and mechanisms

UV photodegradation of 27 typical VOCs was systematically investigated. Contribution of photolysis and photooxidation to VOCs removal was identified. Gaseous VOC could be partially converted to particles by 185/254 nm UV irradiation. The mineralization and conversion of 27 VOCs by UV irradiation were reported. Photodegradation by ultraviolet irradiation (UV) is increasingly applied in volatile organic compound (VOC) and odor gas treatments. In this study, 27 typical VOCs, including 11 hydrocarbons and 16 hydrocarbon derivatives, at 150–200 ppm in air and nitrogen gas were treated by a laboratory-scale UV reactor with 185/254 nm irradiation to systematically investigate their removal and conversion by UV irradiation. For the tested 27 VOCs, the VOC removal efficiencies in air were within the range of 13%–97% (with an average of 80%) at a retention time of 53 s, which showed a moderate positive correlation with the molecular weight of the VOCs (R = 0.53). The respective contributions of photolysis and photooxidation to VOC removal were identified for each VOC. According to the CO₂ results, the mineralization rate of the tested VOCs was within the range of 9%–90%, with an average of 41% and were negatively correlated to the molecular weight (R = -0.63). Many of the tested VOCs exhibited high concentration particulate matters in the off-gases with a 3–283 mg/m³ PM₁₀ range and a 2–40 mg/m³ PM_2.5 range. The carbon balance of each VOC during UV irradiation was analyzed based on the VOC, CO₂ and PM₁₀ concentrations. Certain organic intermediates and 23–218 ppm ozone were also identified in the off-gases. Although the UV technique exhibited a high VOC removal efficiency, its drawbacks, specifically low mineralization, particulate matters production, and ozone emission, must be considered prior to its application in VOC gas treatments.     

Chemical speciation and anthropogenic sources of ambient volatile organic compounds (VOCs) during summer in Beijing, 2004

Volatile organic compounds (VOCs) were measured at six sites in Beijing in August, 2004. Up to 148 VOC species, including C₃ to C₁₂ alkanes, C₃ to C₁₁ alkenes, C₆ to C₁₂ aromatics, and halogenated hydrocarbons, were quantified. Although the concentrations differed at the sites, the chemical compositions were similar, except for the Tongzhou site where aromatics were significantly high in the air. Based on the source profiles measured from previous studies, the source apportionment of ambient VOCs was preformed by deploying the chemical mass balance (CMB) model. The results show that urban VOCs are predominant from mobile source emissions, which contribute more than 50% of the VOCs (in mass concentrations) to ambient air at most sites. Other important sources are gasoline evaporation, painting, and solvents. The exception is at the Tongzhou site where vehicle exhaust, painting, and solvents have about equal contribution, around 35% of the ambient VOC concentration. As the receptor model is not valid for deriving the sources of reactive species, such as isoprene and 1,3-butadiene, other methodologies need to be further explored.     

Volatile organic compounds of Acacia longifolia and their effects on germination and early growth of species from invaded habitats

Acacia longifolia, a highly invasive species that invades coastal ecosystems in Mediterranean areas, produces significant impacts at different scales. Abundant foliage and thick canopies create a dense atmosphere that led us to hypothesise that the release of volatile organic compounds (VOCs) could play a role in the reduction of biodiversity observed in invaded areas. Therefore, we suggested that VOCs emitted by A. longifolia could exert inhibitory effects on physiological and biochemical parameters of native species. Using glass chamber bioassays, we evaluated the effect of aerial contact between VOCs from different plant parts of A. longifolia material and some native species. Volatile chemical composition was further analysed using GC-MS. Our results indicated that VOCs produced a notably reduction of seed germination. Furthermore, volatiles from leaves and flowers significantly decreased root length, shoot length and biomass for all species. Proline and malondialdehyde content did not significantly increase after contact with VOCs. Finally, chemical profile of VOCs from flowers, leaves and litter was significantly different, both qualitatively and quantitatively. As far as we know, our results constitute the first evidence of phytotoxicity induced by VOCs from A. longifolia, suggesting that flowers and leaves could influence its surrounding environment through VOCs release.     

Indoor air quality in elementary schools of Lisbon in spring

Analysis of indoor air quality (IAQ) in schools usually reveals higher levels of pollutants than in outdoor environments. The aims of this study are to measure indoor and outdoor concentrations of NO₂, speciated volatile organic compounds (VOCs) and carbonyls at 14 elementary schools in Lisbon, Portugal. The investigation was carried out in May–June 2009. Three of the schools were selected to also measure comfort parameters, such as temperature and relative humidity, carbon dioxide (CO₂), carbon monoxide (CO), total VOCs, and bacterial and fungal colony-forming units per cubic metre. Indoor concentrations of CO₂ in the three main schools indicated inadequate classroom air exchange rates. The indoor/outdoor (I/O) NO₂ ratio ranged between 0.36 and 0.95. At the three main schools, the total bacterial and fungal colony-forming units (CFU) in both indoor and outdoor air were above the advised maximum value of 500 CFU/m³ defined by Portuguese legislation. The aromatic compounds benzene, toluene, ethylbenzene and xylenes, followed by ethers, alcohols and terpenes, were usually the most abundant classes of VOCs. In general, the indoor total VOC concentrations were markedly higher than those observed outdoors. At all locations, indoor aldehyde levels were higher than those observed outdoors, particularly for formaldehyde. The inadequate ventilation observed likely favours accumulation of pollutants with additional indoor sources.     

Screening the emission sources of volatile organic compounds (VOCs) in China by multi-effects evaluation

We develop a multi-effect evaluation method to assess integrated impact of VOCs. Enable policy-makers to identify important emission sources, regions, and key species. Solvent usage and industrial process are the most important anthropogenic sources. Styrene, toluene, ethylene, benzene, and m/p-xylene are key species to be cut. Volatile organic compounds (VOCs) play important roles in the atmosphere via three main pathways: photochemical ozone formation, secondary organic aerosol production, and direct toxicity to humans. Few studies have integrated these effects to prioritize control measures for VOCs sources. In this study, we developed a multi-effects evaluation methodology based on updated emission inventories and source profiles, by combining the ozone formation potential (OFP), secondary organic aerosol potential (SOAP), and VOC toxicity data. We derived species-specific emission inventories for 152 sources. The OFPs, SOAPs, and toxicity of each source were estimated, the contribution and sharing of source to each of these adverse effects were calculated. Weightings were given to the three adverse effects by expert scoring, and then the integrated effect was determined. Taking 2012 as the base year, solvent use and industrial process were found to be the most important anthropogenic sources, accounting for 24.2% and 23.1% of the integrated effect, respectively, followed by biomass burning, transportation, and fossil fuel combustion, each had a similar contribution ranging from 16.7% to 18.6%. The top five industrial sources, including plastic products, rubber products, chemical fiber products, the chemical industry, and oil refining, accounted for nearly 70.0% of industrial emissions. Beijing, Chongqing, Shanghai, Jiangsu, and Guangdong were the five provinces contributing the largest integrated effects. For the VOC species from emissions showed the largest contributions were styrene, toluene, ethylene, benzene, and m/p-xylene.     

Floral scent variation in two <Emphasis Type="Italic">Antirrhinum majus</Emphasis> subspecies influences the choice of naïve bumblebees

Two wild subspecies of snapdragon, Antirrhinum majus, subspecies pseudomajus and striatum, differ in floral color and can be visually discriminated by insect visitors. The extent to which olfactory cues derived from floral scents contribute to discrimination between snapdragon subspecies is however unknown. We tested whether these two subspecies differ in floral scent and whether these olfactory differences are used by bumblebees (Bombus terrestris) to discriminate between them. We grew individuals of both subspecies, collected from a total of seven wild populations, under controlled conditions. We quantified the volatile organic compounds (VOCs) emitted by the flowers using gas-chromatography/mass-spectrometry/flame-ionization-detection. We studied antennal detection of VOCs by bumblebees, by means of electroantennogram study (EAG). We also performed behavioral experiments in a Y-maze to determine the innate response of bumblebees to the main floral VOCs emitted by our snapdragon subspecies. The floral scent of Antirrhinum majus pseudomajus contained three volatile benzenoids absent in the floral scent of Antirrhinum majus striatum. One of them, acetophenone, contributed over 69% of the absolute emissions of A. majus pseudomajus. These benzenoids elicited a significantly higher EAG response compared with other VOCs. In the Y-maze, bumblebees were significantly less attracted by acetophenone, suggesting an aversive effect of this VOC. Our findings indicate that bumblebees are able to discriminate between the two Antirrhinum majus subspecies. Differences in flower scent between these subspecies and olfactory bumblebee preferences are discussed in the light of biochemical constraints on VOCs synthesis and of the role of flower scent in the evolutionary ecology of A. majus.     

Selenium speciation in wheat grain varies in the presence of nitrogen and sulphur fertilisers

This study investigated whether selenium species in wheat grains could be altered by exposure to different combinations of nitrogen (N) and sulphur (S) fertilisers in an agronomic biofortification experiment. Four Australian wheat cultivars (Mace, Janz, Emu Rock and Magenta) were grown in a glasshouse experiment and exposed to 3 mg Se kg^?1 soil as selenate (Se^VI). Plants were also exposed to 60 mg N kg^?1 soil as urea and 20 mg S kg^?1 soil as gypsum in a factorial design (N + S + Se; N + Se; S + Se; Se only). Plants were grown to maturity with grain analysed for total Se concentrations via ICP-MS and Se species determined via HPLC-ICP-MS. Grain Se concentrations ranged from 22 to 70 µg Se g^?1 grain (dry mass). Selenomethionine (SeMet), Se-methylselenocystine (MeSeCys), selenohomolanthionine (SeHLan), plus a large concentration of uncharacterised Se species were found in the extracts from grains. SeMet was the major Se species identified accounting for between 9 and 24 µg Se g^?1 grain. Exposure to different N and S fertiliser combinations altered the SeMet content of Mace, Janz and Emu Rock grain, but not that of Magenta. MeSeCys and SeHLan were found in far lower concentrations (<4 µg Se g^?1 grain). A large component of the total grain Se was uncharacterisable (>30 % of total grain Se) in all samples. When N fertiliser was applied (with or without S), the proportion of uncharacterisable Se increased between 60 and 70 % of the total grain Se. The data presented here indicate that it is possible to alter the content of individual Se species in wheat grains via biofortification combined with manipulation of N and S fertiliser regimes. This has potential significance in alleviating or combating both Se deficiency and Se toxicity effects in humans.     

Effects of phosphorus sources on volatile organic compound emissions from <Emphasis Type="Italic">Microcystis flos</Emphasis>-<Emphasis Type="Italic">aquae</Emphasis> and their toxic effects on <Emphasis Type="Italic">Chlamydomonas reinhardtii</Emphasis>

There is diverse phosphorus (P) in eutrophicated waters, but it is considered as a crucial nutrient for cyanobacteria growth due to its easy precipitation as insoluble salts. To uncover the effects of complex P nutrients on the emission of volatile organic compounds (VOCs) from cyanobacteria and their toxic effects on other algae, the VOCs from Microcystis flos-aquae supplied with different types and amount of P nutrients were analyzed, and the effects of VOCs and their two main compounds on Chlamydomonas reinhardtii growth were investigated. When M. flos-aquae cells were supplied with K₂HPO₄, sodium pyrophosphate and sodium hexametaphosphate as the sole P source, 27, 23 and 29 compounds were found, respectively, including furans, sulfocompounds, terpenoids, benzenes, aldehydes, hydrocarbons and esters. With K₂HPO₄ as the sole P source, the VOC emission increased with reducing P amount, and the maximum emission was found under Non-P condition. In the treatments of M. flos-aquae VOCs under Non-P condition and two main terpenoids (eucalyptol and limonene) in the VOCs, remarkable decreases were found in C. reinhardtii cell growth, photosynthetic pigment content and photosynthetic abilities. Therefore, we deduce that multiple P nutrients in eutrophicated waters induce different VOC emissions from cyanobacteria, and P amount reduction caused by natural precipitation and algal massive growth results in more VOC emissions. These VOCs play toxic roles in cyanobacteria becoming dominant species, and eucalyptol and limonene are two toxic agents.     

Genetic variability in triticale x bread wheat derivatives under normal and phosphorus stress regimes

Twenty six hexaploid triticale (X Triticosecale Wittmack) X bread wheat (Triticum aestivum L. em Thell) derivatives, along with 2 bread wheat and 2 triticale checks, were grown in normal and P-stress environments. Spikes/plant and grain yield/plant, followed by peduncle length, Were the most sensitive to phosphorus deficiency, which also caused a delay in heading and maturity. The heritability and genetic advance for grain yield/plant were high in the stress environment, reflecting the effectiveness of direct selection. The 1000-grain weight, grains/spike and plant height were the important traits for phenotypic selections in both the environments.     

地下水中VOC挥发因子模型的研究

建立了一个计算地下水中挥发性有机物（VOC）挥发因子的模型.选用半挥发性的1,2,4-三氯苯和挥发性的四氯乙烯为VOC的代表,分别计算了非饱和区土壤为砂土和粘土时的挥发因子.结果表明：蒸发使VOC的挥发因子增大,而下渗则使VOC的挥发因子减小;不论VOC的挥发性强弱,蒸发（下渗）对挥发因子的影响均比较明显;蒸发情况下,非饱和区土壤性质对挥发因子的影响不明显,而下渗情况下,非饱和区土壤性质对挥发因子的影响则趋于明显;此外,当非饱和区土壤为粘土时,VOC的挥发因子受蒸发（下渗）的影响更明显.     

根表铁膜对水稻铅吸收转运的影响

通过温室土壤盆栽试验研究不同生育期水稻根表铁膜形成对水稻吸收和转运Pb的影响。结果表明,两种水稻根表铁膜形成量(以DCB-Fe含量计)及铁膜中吸附的Pb量均随着生育期的延长而减少。水稻根表铁膜Fe含量与铁膜吸附的Pb量呈显著的正相关关系(r=0.798,p0.01)。水稻根系和茎叶吸收积累Pb随着不同品种和不同生育期而变化。品种NK57籽粒Pb含量显著高于品种YD6,前者为后者的1.9倍。从富集系数和分配比率来看,Pb主要富集在水稻的铁膜和根系中,而积累在茎叶和籽粒中的比率较少。Pb从水稻根表铁膜、根系和茎叶向籽粒中的转运系数在两个水稻品种间差异均不显著。水稻分蘖期和孕穗期根表铁膜量与根系Pb含量均呈显著的正相关关系(p0.05),但是成熟期水稻根表铁膜量与根系、茎叶和籽粒中Pb含量相关性均不显著,说明根表铁膜形成对水稻分蘖期和孕穗期吸收积累Pb有一定影响,但对水稻成熟期根系、茎叶和籽粒吸收积累Pb影响不大。     

Maize field odorscape during the oviposition flight of the European corn borer

Most crop pests find a suitable host through chemical cues released from plants, but little is known about the odorscape encountered by host-seeking gravid females under natural, outdoor conditions. In this field study, the volatile organic compound (VOC) composition of maize (Zea mays, L.), a host for the European corn borer (ECB) (Ostrinia nubilalis Hüb.) was characterized during the oviposition flight and compared with a forest odorscape. VOCs from maize fields and the forest atmosphere were collected by solid phase microextraction and characterized by gas chromatography-mass spectrometry. The electroantennographic (EAG) response of female ECB antennae to candidate VOCs was tested. Analyses revealed clear differences between the maize field and the forest odorscapes, mainly composed of ubiquitous VOCs but in specific ratios. The maize field odorscape is more complex than the forest odorscape for maize found 18 VOCs but only eight in the forest. Both biotopes shared seven VOCs—green leaf volatiles (GLV), monoterpènes (MT) and homoterpenes. In addition, we found in the forest a distinctive sesquiterpene (SQT) identified as isoledene. The highest EAG responses were elicited by two GLVs and a MT shared by the two biotopes. SQT elicited weak EAG responses, except β-farnesene, only found in the maize field odorscape. Our results suggest that the two biotopes produce specific chemical signatures that insects may use as host cues. To the best of our knowledge this paper is the first report on the maize odorscapes under field conditions. The putative role of the VOCs in host plant detection and selection is discussed.     

不同品种水稻对Cu积累分配的差异

以21个水稻品种（包括常规稻、二系杂交稻、三系杂交稻）为材料,通过室内盆栽试验探讨了Cu在不同品种水稻根-茎-叶-籽粒（糙米）中的积累分配的差异。结果表明,供试水稻品种根、茎、叶、籽粒中Cu含量的均值分别是67.35、16.24、8.29、11.62mg·kg-1,多数水稻品种Cu的含量顺序是根茎籽粒（糙米）叶,但也有少部分水稻品种Cu的含量顺序是根籽粒（糙米）茎叶。各器官的Cu含量在不同品种间存在显著差异,其中以根和籽粒Cu含量的差异最大,茎次之,叶最小。常规稻根部Cu含量显著低于杂交稻,而叶中Cu含量显著高于杂交稻,但两者的茎和籽粒中Cu含量没有明显的差异。三系杂交稻根、茎、籽粒Cu含量显著高于二系杂交稻,而叶的Cu含量两者差异不显著。不同遗传背景的水稻各器官对Cu积累也存在不同程度的差异。相关分析结果表明,不同品种水稻相邻器官（根与茎,茎与叶）的Cu含量呈极显著正相关,相间器官（根与叶、籽粒,茎与籽粒）的Cu含量呈显著正相关,地上部各器官Cu的转运系数相互之间呈极显著的正相关。     

2种常规水稻Cd、Zn吸收与器官分配的生育期变化：品种、土壤和Cd处理的影响

Cd在土壤-作物-膳食食物链中的迁移是人类对环境Cd暴露及其健康风险的主要途径,而水稻是子粒Cd积累最强的大宗作物之一.采用全生育期淹水盆栽试验研究了2种常规水稻(高Cd吸收品种“苏香粳1号”和低Cd吸收品种“99-22”)在添加Cd(2mg·kg-1)和不添加Cd处理下对2种土壤(红沙泥田,乌栅土)中Cd、Zn的吸收及其生育期变化.结果表明:1)常规水稻对Cd、Zn的吸收积累受土壤、品种和外源Cd的影响.Cd处理、土壤、品种间的正交互作用(高Cd吸收品种植于高Cd处理且Cd有效性高的红壤中)使常规稻植株Cd/Zn比成数十倍提高,从而使子粒Cd/Zn比产生强烈升高;2)水稻对Cd、Zn的吸收强度因不同生育期而异,Cd吸收的主要时期是分蘖期和成熟期,而Zn吸收的主要时期则是分蘖期、抽穗期和灌浆期.在整个生育期中,水稻Cd吸收伴随着对Zn的排斥现象,这在高Cd吸收下尤为强烈;3)水稻各器官对Cd、Zn的吸收分配无论是同品种的生育期间抑或同生育期时的不同品种间均有显著差异.Cd积累量为根系>穗粒>茎叶,而Zn却表现为茎叶>根系、穗粒.观察到水稻吸收的Cd在生育后期向穗粒的强烈运移.相对于低Cd吸收品种来说,Cd向穗粒转运较强,而Zn的转运较弱是高Cd吸收品种子粒Cd积累强而Cd/Zn比高的植株因素.     

预浓缩/柱箱制冷GCMS/FID法测定大气中117种挥发性有机物

建立了罐采样、吸附剂辅助电子制冷预浓缩-柱箱制冷GCMS/FID同时测定大气中117种挥发性有机物(VOCs)的方法。样品经填充吸附剂的电子制冷预浓缩系统除水、除CO₂、浓缩和热脱附后,采用柱箱制冷及GCMS/FID的多维切割单元,将5种C₂-C₃组分切到二维色谱柱进行分离并进入FID检测,甲醛及其他111种VOCs组分留在一维色谱柱进行分离并进入MS检测,甲醛采用SIM模式检测,其余化合物采用Scan模式检测。FID采用外标法定量,MS采用内标法定量。考查了预浓缩系统条件、多维切割条件、质谱条件、气相条件等参数对测试结果的影响,对比了常温柱箱法和柱箱制冷法的效果,并评估了在此优化条件下的方法性能。117种VOCs在0.5—20 nmol·mol^-1(甲醛2.5—100 nmol·mol^-1)范围内线性关系良好,相关系数(R)在0.9924—0.9999,方法检出限为0.071—0.718μg·m^-3,定量限为0.284—2.872μg·m^-3。     

易挥发有机化合物在Pt/Al_2O_3-Si纤维催化剂上的低温氧化

本文合成了一种新型的Pt负载在Al_2O_3涂膜强力富硅纤维载体的催化剂,研究低温下催化易挥发有机化合物的行为.用四种有机化合物检验实验参数对催化剂分解有机化合物分解率的影响.讨论了流速、浓度、有机物的本性、预热温度、反应热等参数的影响,并给出了催化剂对苯、甲苯在特定实验条件下的活化能、反应级数和指前因子的数值.     

厦门市隧道中挥发性有机物污染研究

选择厦门市典型的7个隧道,采用三段预浓缩和气相色谱-质谱联用方法,对隧道口和隧道内空气中的VOCs进行了分析研究。结果表明：隧道内VOCs污染一般比隧道口严重,而当隧道口受到周围VOCs污染的影响时,将导致隧道口VOCs污染比隧道内严重;甲苯、乙醇、对二甲苯、邻二甲苯、1,2,4-三甲苯为本研究主要的活性组分,甲苯对隧道空气的光化学活性贡献最大;BTEX分析显示,除汽车尾气外,其它源也会对隧道内苯系物的污染有较大的影响;对隧道内和隧道口VOCs相关性分析发现,1,3-丁二烯、丙烯醛、二氯甲烷、正己烷、1,1-二氯乙烷、4-乙基甲苯、氟利昂-12、一氯甲烷的相关性较好,表明在隧道内和隧道口这些物质具有相同的来源。     

烟草对砷的吸收累积特征及其健康风险研究

以福建省主栽烟草品种翠碧1号、K326和云烟87为材料,在外源砷添加量为0、10、20、40、70和100 mg·kg~(-1)的土壤中进行盆栽试验,探讨砷对烟草的毒害效应以及砷在土壤-烟草体系中的迁移累积特征,并对植烟土壤中砷的安全临界值进行计算。结果表明,在砷毒害下,烟草生长受到抑制,且烟草根系生长受抑制程度最强。随着砷添加量的增加,土壤中有效砷含量和烟草各部位砷含量均显著提高(P 0.05),砷在根系中的含量最高,在茎中的含量最低。砷处理下各部位间的转移系数表现为TF_((茎-叶)) TF_((土-根)) TF_((根-茎)),且外源砷的增加促进砷从茎到叶片中转移。38.28%～74.37%的砷富集在烟草根部,上部叶中砷的富集量最少(4.61%～11.7%),且所研究的3个烟草品种中翠碧1号对砷的富集能力最强。根据通过吸烟进入人体砷的限量以及土壤有效砷含量与烟草中部叶砷含量的回归模型,推算出翠碧1号、K326和云烟87的植烟土壤有效砷的安全临界值分别为14.17、14.31和11.86 mg·kg~(-1)(磷酸二氢钠浸提)。并将福建省植烟土壤有效砷的安全临界值拟定为11.86 mg·kg~(-1)(磷酸二氢钠浸提)。本研究结果为福建省烟草安全生产提供一定技术指导。     

污泥好氧发酵过程中挥发性有机物（VOCs）污染风险研究

污泥好氧堆肥发酵过程所产生的可挥发性有机物已经成为重要的二次污染物,采用气质联用（GC/MS）的方法分析了郑州某污泥处置厂发酵车间不同位置的挥发性有机物（VOCs）组分。结果表明：污泥堆肥过程可检测出的VOCs共有19种,主要致臭组分是甲硫醇、二甲二硫醚、甲硫醚,它们在所有采气点中的质量浓度均高于检知嗅阈值,对人类嗅觉具有较大危害;总挥发性有机物（TVOC）的质量浓度由堆体内部产生时的47.2 mg·m-3,降为车间工人活动处的1.73 mg·m-3,迁移过程中总浓度减少了96.3%;利用最大增量反应活性法研究VOCs的反应活性和对近地层臭氧的生成潜势影响,VOCs组分中烷烃、芳香烃、酮类、烯烃类的最大臭氧生成潜势值依次增加,其中,最大臭氧生成潜势值（OFP）贡献量最高的组分为1-丁烯和丙烯,OFP分别达到了947.70μg·m-3和875.67μg·m-3,存在大气污染风险。通过主要VOCs组分间的相关性分析,发现甲硫醇宜作为评估VOCs排放情况的指示气体,其在工人活动处的质量浓度为0.04 mg·m-3,远低于GBZ 2—2002《工作场所有害因素职业接触限值》所规定的2.5 mg·m-3限量值。