空气清新剂中挥发性有机物的组成及其对室内空气质量的潜在影响

研究调查了广州市各大型超市销售的14个品牌,15种不同香型,共26个盒装空气清新剂中挥发性有机物（VOCs）的成分.通过顶空GC-MS分析获得的结果可以看出各个空气清新剂的成分组成差别较大,即使是相同香型的产品,其中的化合物种类和百分比浓度都不尽相同.定性出94种化合物,包括烯烃18种,醇类15种,醛类14种,酮类4种,醚类5种,酚类1种,酯类25种及其它化合物12种,其中萜类化合物约占总化合物数量的40%.β-月桂烯、罗勒烯、苧烯、苯乙醇、乙酸苄酯、β-蒎烯、β-水芹烯、伞花烃、1-甲基-4-（1-甲基乙烯基）苯、里拉醇等化合物在各种清新剂中出现频率为100%.空气清新剂中萜类化合物与臭氧反应,可生成二次有机气溶胶,对室内空气质量造成影响.     

Optimized porous clay heterostructure for removal of acetaldehyde and toluene from indoor air

Adsorption is the most widely used technology for the removal of indoor volatile organic compounds (VOCs). However, existing adsorbent-based technologies are inadequate to meet the regulatory requirement, due to their limited adsorption capacity and efficiency, especially under high relative humidity (RH) conditions. In this study, a series of new porous clay heterostructure (PCH) adsorbents with various ratios of micropores to mesopores were synthesized, characterized and tested for the adsorption of acetaldehyde and toluene. Two of them, PCH25 and PCH50, exhibited markedly improved adsorption capability, especially for hydrophilic acetaldehyde. The improved adsorption was attributed to their large micropore areas and high micropore-to-mesopore volume ratios. The amount of acetaldehyde adsorbed onto PCH25 at equilibrium reached 62.7 mg·g⁻¹, eight times as much as the amount adsorbed onto conventional activated carbon (AC). Even at a high RH of 80%, PCH25 removed seven and four times more of the acetaldehyde than AC and the unmodified raw PCHs did, respectively. This new PCH optimized for their high adsorption and resistance to humidity has promising applications as a cost-effective adsorbent for indoor air purification.     

室内空气中挥发性有机物污染与防治

论述了室内空气质量的重要性以及室内挥发性有机物（VOC）污染来源，介绍了评价V0C污染的量化指标VDC和减少室内VOC污染的措施和技术。     

Post-war levels of persistent organic pollutants (POPs) in air from Serbia determined by active and passive sampling methods

For the duration of the war accident in former Yugoslavia, several industrial and military targets were burnt and damaged, resulting in a significant release of persistent organic pollutants. Locations heavily targeted in the attacks were later defined by UNEP as four “hot spots”: Kragujevac, Novi Sad, Pancevo and Bor. We analyzed concentration levels of pollutants collected in 2004 and 2005 in air samples from the city of Kragujevac, Serbia, following the war accident of 1999. Pollutants included polycyclic aromatic hydrocarbons (PAHs), hexachlorocyclohexane (HCH), dichloro-diphenyl-trichloroethane (DDT), dichloro-diphenyl-dichloroethylene (DDE), dichloro-diphenyl-dichloroethane (DDD) and polychlorinated biphenyls (PCBs). We present results obtained during air sampling campaign conducted in July 2004 by the active sampling method; and during September 2004–June 2005 by the passive sampling method. Our findings show the occurrence of residual quantities of DDT, HCH, PCBs and PAHs in air samples. High levels of PCBs are probably due to the destruction of transformers during the war accident.     

Characteristics of carbonyls and volatile organic compounds (VOCs) in residences in Beijing,China

Volatile organic compounds (VOCs) and carbonyl compounds were measured both indoors and outdoors in 50 residences of Beijing in heating (December, 2011) and non-heating seasons (April/May, 2012). SUMMA canisters for VOCs and diffusive samplers for carbonyl compounds were deployed for 24 h at each site, and 94 compounds were quantified. Formaldehyde, acetone and acetaldehyde were the most abundant carbonyl compounds both indoors and outdoors with indoor median concentrations being 32.1, 21.7 and 15.3 μg·m⁻³, respectively. Ethane (17.6 μg·m⁻³), toluene (14.4 μg·m⁻³), propane (11.2 μg·m⁻³), ethene (8.40 μg·m⁻³), n-butane (6.87 μg·m⁻³), and benzene (5.95 μg·m⁻³) showed the high median concentrations in indoor air. Dichloromethane, p-dichlorobenzene (p-DCB) and toluene exhibited extremely high levels in some residences, which were related with a number of indoor emission sources. Moreover, isoprene, p-dichlorobenzene and carbonyls showed median indoor/outdoor (I/O) ratios larger than 3, indicating their indoor sources were prevailing. Chlorinated compounds like CFCs were mainly from outdoor sources for their I/O ratios being less than 1. In addition, indoor concentrations between two sampling seasons varied with different compounds. Carbonyl compounds and some chlorinated compounds had higher concentrations in the non-heating season, while alkanes, alkenes, aromatic compounds showed an increase in the heating season. Indoor concentration of VOCs and carbonyls were influenced by locations, interior decorations and indoor activities, however the specific sources for indoor VOCs and carbonyls could not be easily identified. The findings obtained in this study would significantly enhance our understandings on the prevalent and abundant species of VOCs as well as their concentrations and sources in Beijing residences.     

室内空气和灰尘中全(多)氟烷基化合物的研究进展

全(多)氟烷基化合物(per(poly)fluoroalkyl substances,PFASs)在环境各个介质及人体样品中广泛被检出,近年,在室内空气和灰尘中也普遍发现PFASs.研究表明,室内空气中PFASs的含量普遍高于室外空气,室内空气和灰尘中的PFASs可能是室外空气的污染来源及人体暴露源,因此室内环境中PFASs成为环境领域的又一个研究热点.但目前为止,我国还没有开展室内空气中PFASs的相关研究,室内灰尘中PFASs的研究也相对较少.本文就室内空气和灰尘中PFASs的采样与分析方法、污染现状、来源分析及人体暴露等4个方面进行了综合阐述,以期为我国室内环境中PFASs的研究提供参考.     

Passive sampling of PAHs in indoor air in Nepal

PAHs were sampled in ten homes in the Makwanpur region, Nepal. SPMDs and moss bags (Sphagnum girgensohnii) were used as passive samplers. Soot particles on the SPMD surfaces were also analyzed for PAHs. The overall PAH concentrations in SPMDs were significantly higher than those in moss bags. Total PAH mean concentrations of ten houses were 535μg/g lipid for SPMDs and 7.2 μg/g moss (dw) for moss bags. Ratios of phenanthrene/anthracene in indoor SPMDs and particulate matter varied from 2.9 to 3.5 and ratios of fluoranthene/pyrene varied from 1.1 to 1.4. The values for moss bags were respectively 1.7–3.6 and 0.8–2.4. These ratios indicate that the PAHs are from combustion origin. The PAH concentrations in ambient air were estimated as B(a)P TEQs and they were 17–64 times higher than acceptable limit for Finnish community air. Based on PAH levels in the gas phase (SPMD) we may expect PAHs to have an impact on respiratory disease prevalence in Nepalese villages. Both of the sampling methods were feasible in the difficult conditions under which the study was performed.     

郑州市环境空气中VOCs的污染特征及健康风险评价

挥发性有机物（VOCs）不但是引发霾和光化学烟雾等环境问题的重要原因,达到一定浓度时还对人类健康造成威胁.为研究中原地区环境空气中VOCs 污染状况,探查VOCs 对人群健康产生的风险,以中原地区核心城市-郑州为代表,于2012年─2013 年间,在郑州市区内布点,以苏玛罐采样/气相色谱-质谱法分析测定了VOCs 的时空分布,并使用健康风险评价四步法进行健康风险评价.郑州市环境空气中VOCs 年均浓度分布特征：以烷烃和芳香烃为主,分别占总量的23.8%和19.5%;年平均质量浓度,芳香烃类为131 μg·m^-3、烷烃类为118 μg·m^-3,酮类为84.3 μg·m^-3、卤代烷烃类为67.8 μg·m-3;单体化合物以丙酮（66.2 μg·m-3）、乙醇（27.5 μ·m-3）、正十-烷（24.4 μg·m-3）和甲苯（17.2 μg·m-3）质量浓度最高,污染程度在国内居于中等水平.VOCs 季均浓度分布特征：夏季高于冬季,但各类化合物在两季的浓度差异较大.VOCs 日均浓度变化特征：烷烃类和芳烃类化合物于10：00 出现浓度峰值,浓度变化趋势与交通量变化具有相关性.健康风险评价结果为：非致癌风险大于1,会对人群健康造成-定的非致癌危害;苯、四氯化碳、1,2-二氯乙烷、1,1,2-三氯乙烷、六氯丁二烯的致癌指数超过EPA 致癌风险值,但未超出OSHA 致癌风险.     

两种常见植物净化室内空气的效果

为探讨家居植物对甲醛的吸收能力和对改善室内空气质量的效果,将库拉索芦荟（Aloevera）和虎尾兰（Sansevieria trifasciata）两种植物放置于相对封闭的环境中,进行16d的甲醛暴露实验。结果表明,虎尾兰的甲醛耐受性高于库拉索芦荟,在整个实验过程中都保持良好的生长状态,具有持续的甲醛去除能力（去除率达...     

Occurrence of benzotriazoles (BTRs) in indoor air from Albany,New York,USA, and its implications for inhalation exposure

Despite the widespread use of benzotriazoles as corrosion inhibitors in many household goods, studies on the occurrence of these compounds in indoor air are scarce. In this study, five benzotriazole derivatives were measured in 83 indoor air samples collected from various locations in Albany, New York, USA. Benzotriazoles were found in a majority of the indoor air samples, and the concentrations of their sum in bulk (vapor plus particulate phases) indoor air ranged from below the method limit of quantification to 492 ng·m^?3 (geometric mean: 5.8 ng·m^?3). The highest geometric mean concentration was found in air samples collected in parking garages (155 ng·m^?3), followed by barbershops (13.6), public places (11.5), auto repair shops (5.2), automobiles (4.5), homes (4.5), offices (3.7), and laboratories (2.8). Inhalation exposure to benzotriazoles was calculated on the basis of the measured geometric mean concentrations and air inhalation rate. The highest exposure dose was found for teenagers, with a geometric mean inhalation exposure dose of 79 ng·day^?1. The body-weight normalized exposure dose, however, was the highest for infants, at 3.2 ng·(kg bw)^?1·day^?1.     

Levels of selected urinary metabolites of volatile organic compounds in a representative sample of US adolescents

Data from National Health and Nutrition Examination Survey for the years 2011–2012 were used to evaluate the variability in the observed levels of 20 urinary metabolites of 16 parent volatile organic compounds by age, gender, race/ethnicity, and smoking status for adolescents aged 12–19 years. Smokers were found to have statistically significantly higher adjusted levels than nonsmokers for selected urinary metabolites of acrylonitrile (p < 0.05) and 1,3-butadiene (p < 0.05). For example, for N-Acetyl-S-(2-cyanoethyl)-L-cysteine, the adjusted levels for smokers were 29.2 ng/mL and 2.0 ng/mL for nonsmokers (p < 0.05). Females were found to have higher adjusted levels of selected metabolites of crotonaldehyde (p < 0.05), cyanide (p < 0.05), and tetrachloroethylene (p < 0.05) than males. For example, the adjusted levels of 2-Aminothiazoline-4-carboxylic acid or ATCA were 218.9 and 108.6 ng/mL for females and males, respectively (p < 0.05). Non-Hispanic whites (NHW) had higher adjusted levels than non-Hispanic blacks (NHB) for selected metabolites of N,N-dimethylformamide (p < 0.05) and ethylbenzene, styrene (p < 0.05). For example, for N-Acetyl-S-(N-methylcarbamoyl)-L-cysteine or AMCC, the adjusted levels for NHW and NHB were 122.7 and 80.2 ng/mL, respectively (p < 0.05). The reverse was true for selected metabolites of carbon-disulfide and tetrachloroethylene. For example, for N-Acetyl-S-(benzyl)-L-cysteine or BMA, adjusted levels for NHW and NHB were 6.7 and 10.3 ng/mL, respectively (p < 0.05).     

Target the neglected VOCs emission from iron and steel industry in China for air quality improvement

● Haze formation in China is highly correlated with iron and steel industry. ● VOCs generated in sinter process were neglected under current emission standard. ● Co-elimination removal of sinter flue gas complex pollutants are timely needed. Recent years have witnessed significant improvement in China’s air quality. Strict environmental protection measures have led to significant decreases in sulfur dioxide (SO₂), nitrogen oxides (NO_x), and particulate matter (PM) emissions since 2013. But there is no denying that the air quality in 135 cities is inferior to reaching the Ambient Air Quality Standards (GB 3095–2012) in 2020. In terms of temporal, geographic, and historical aspects, we have analyzed the potential connections between China’s air quality and the iron and steel industry. The non-target volatile organic compounds (VOCs) emissions from iron and steel industry, especially from the iron ore sinter process, may be an underappreciated index imposing a negative effect on the surrounding areas of China. Therefore, we appeal the authorities to pay more attention on VOCs emission from the iron and steel industry and establish new environmental standards. And different iron steel flue gas pollutants will be eliminated concurrently with the promotion and application of new technology.     

大气中氟化物污染的生物学指标监测评价

植物对HF气体的敏感性是由多种因素相互作用而成的复杂综合性状,常用于定性描述大气环境质量状况。通过在密闭的培养瓶中一次性通入不同体积浓度的HF气体,以不同浓度HF胁迫下的不同类型植物为例,观察其在不同时间的外观伤害症状和细胞膜透性与HF浓度的关系。结果表明：不同植物对HF的敏感性不同;低浓度长时间和高浓度短时间的症状基本相同;植物细胞膜透性数据即电导率直接反映植物受损程度。综合植物外观症状指标与生理生化指标并赋予不同权重值,建立相对定量化的大气质量生物学指标评价模式,以定量的判断HF气体对植物的伤害,为应用植物监测和评价大气环境质量提供理论和实践依据。     

Photochemical transformations of selected organic chemicals in two phase system

The photodegradation of some aromatic sulfur compounds dissolved in n‐hexane and spread as a thin liquid film on water was investigated. Dibenzothiophene and diphenylsulfide were found to be the most reactive towards photooxidation process among the compounds studied. The degraded compounds were investigated by HPLC and GC/MS.     

山东重点城市空气质量及其与气象要素的关系

利用山东省济南、青岛2001—2010年以及其他7个重点城市2005—2010年逐日空气污染指数（API）和同期的常规气象资料,运用统计方法,分析了各市空气质量年、季变化特征,并利用SPSS软件进一步分析探讨了API指数与风速、气温、降水、湿度、日照时数等气象因子的相关关系。结果表明：济南由于受能源结构、地形、气象条件等因素的影响,API指数累年平均值最大达到91.2,沿海城市空气质量明显好于内陆城市,日照 API 指数最小仅为56.5;从年际变化来看,济南由于加强对空气污染的治理,空气质量明显改善,API指数呈逐年下降趋势,其他城市有不同程度的增加或减小。空气质量具有明显的季节变化,各城市均是夏季空气质量最好,优良率天数频率最多,冬季最差,济南冬季发生轻微污染以上天数的频率最大占39.8%;各城市均以 PM10为首要污染物出现的频率为最多,出现以 NO2、SO2为首要污染物频率最多的城市分别是枣庄、潍坊,出现空气质量为优频率最多的城市是日照;各城市4季 API 指数与同期常规气象要素密切相关,4季API指数与降水均呈负相关,除济南春季外,与风速基本呈负相关,春、夏、秋3个季节API指数与相对湿度基本均成负相关,冬季API指数与日照时数成负相关、与气温、相对湿度成正相关。     

大气中持久性有机污染物的采样技术进展

大气是全球持久性有机污染物(persistent organic polutants,POPs)监测的重要环境介质,大气中POPs的采样技术是准确表征大气中POPs赋存水平的关键所在。近年来大气中POPs的采样技术发展很快。本文介绍了大气中POPs的两类采样方法:主动采样法(active air sampling,AAS)和被动采样法(passive air sampling,PAS),总结了新型吸附材料和新型采样器研发的成果,讨论了不同类型的采样方法的特点,对比分析了不同采样方法获得的POPs监测数据,并提出今后应用不同POPs大气采样技术在监测数据可对比性研究方面值得关注的问题。     

沙尘与大雾天气对京津石空气质量影响

采用北京、天津、石家庄2001-2010年沙尘与大雾天气的统计数据以及城市空气污染指数（API）,分析北京、天津、石家庄3市空气污染指数变化特征及大雾和沙尘天气下北京、天津、石家庄3市空气质量情况,进而得出沙尘大雾天气对京津石空气质量的影响。结果表明：2001-2010年间北京、天津、石家庄3市API总体呈下降趋势,天津、石家庄相对于北京空气质量改善较为明显,且空气质量夏季〉秋季〉春冬季。沙尘天气条件下,北京、天津、石家庄3市API平均值分别为255、179和167,空气质量出现良的比率天津为24%,北京、石家庄为10%左右,出现重污染的比率北京高达50%以上,天津和石家庄均在20%左右;3市沙尘天气高频次均出现在3-5月份,但北京沙尘天气发生次数远大于天津和石家庄。大雾天气条件下,北京、天津、石家庄3市API平均值为185、130和167,空气质量出现优或良的比率：天津〉石家庄〉北京,北京和石家庄出现重污染的比率均接近30%,天津不到10%,所以大雾天气对3市空气质量影响较小,大雾天气频次的变化波动并未对该地区空气质量的年际变化造成显著影响,3市高频次大雾天气集中在10-12月份,对该时段内空气污染呈现加重趋势有一定的贡献。所以沙尘和大雾天气均对北京、天津和石家庄空气质量存在不利影响,其中对北京影响最为严重,对天津影响最轻。整体上沙尘对3市的空气质量影响较大,大雾天气影响较小。     

北京市大气挥发性有机物(VOCs)的污染特征及来源

挥发性有机物(VOCs)的排放是大气污染的重要来源,已经成为我国最重要的环境问题之一,北京市的污染尤为严重。本文对北京市近年来大气挥发性有机物、苯系物的污染情况和来源以及不同控制措施下挥发性有机物的浓度变化进行了总结概括,并对今后的研究进行了展望。     

Characteristics of major volatile organic hazardous air pollutants in the urban air of Kaohsiung city

The concentrations and characteristics of volatile organic hazardous air pollutants (HAPs) in the urban city of Kaohsiung from motor vehicles and dense pollutant sources has become a national concern. To continuously monitor volatile organic HAPs, sampling sites were selected near the four air-quality monitoring stations established by Ethe nvironmental Protection Administration of Taiwan ROC, namely Nan-tz, Tso-ying, San-min and Hsiao-kang, from north to south. An on-site automated online monitor of volatile organic compounds (VOCs) was used for continuous monitoring. This study performed two consecutive days of 24-h monitoring of five volatile organic HAPs form August to October 2005 at the four monitoring sites, which cover the northern, central, and southern areas of Kaohsiung city. The average monitored concentration was 2.78–4.84 ppb for benzene, 5.90–9.66 ppb for toluene, 3.62–5.90 ppb for ethylbenzene, 3.73–5.34 ppb for m,p-xylene, 3.38–4.22 ppb for o-xylene, and 4.48–7.00 ppb for styrene. The average monitored concentrations of the major volatile organic HAPs tended to follow the pattern San-min > Nan-tz > Hsiao-kang > Tso-ying. Among all the species monitored in this study, toluene had the highest ambient concentration, followed by styrene, m,p-xylene, ethylbenzene, o-xylene, and benzene. The results showed that the concentration at night was higher than that in the day for toluene at Nan-tz, San-min, Hsiao-kang, and for benzene at Nan-tz and Hsiao-kang.     

广州市饮用水中挥发性有机物的研究

饮用水中的挥发性有机化合物（VOCs）来源于水源水受到的环境污染或是在净化消毒工艺处理工程中反应产生的副产物,可对人体健康造成极大的危害。改革开放以来,广州人口和经济得到突飞猛进的发展,也带来了包括饮用水安全在内的诸多严重的社会和环境问题。虽然饮用水中VOCs的研究已经得到越来越多的重视,但是目前对广州市饮用水中挥发性有机物的研究还鲜有报道。本文在广州市中心城区选取15个不同位置的采样点进行了自来水水样采集,并利用吹扫-捕集-气相色谱-质谱（GC-MS）联用系统分析技术测定水中 VOCs 的种类和三卤甲烷的质量浓度。结果表明,广州市中心城区的自来水中VOCs有20种,以三卤甲烷（THMs）和芳香烃类为主,占了所检出的物质总量的78%以上。THMs中四种化合物（氯仿、一溴二氯甲烷、二溴一氯甲烷、溴仿）的检出率达100%,总三卤甲烷的平均质量浓度为46.46μg· L-1,最大值为53.31μg· L-1,最小值39.91μg· L-1。根据2006版国家饮用水标准,四种三卤甲烷质量浓度均低于标准限值,符合标准要求。对市面上一般的瓶装水的研究发现,瓶装水中三卤甲烷的质量浓度非常低,总三卤甲烷平均质量浓度仅为1.47μg·L-1,约是自来水中质量浓度的1/30。为了解温度及煮沸对自来水中 THMs 质量浓度的影响,本研究设计了实验进行探究。结果发现加热至沸腾过程中,THMs质量浓度随温度升高而升高,而沸腾后THMs骤降,煮沸5 min可降低水中约95%的THMs,接近瓶装水中THMs质量浓度。