泰安降水中多环芳烃的浓度分布和来源分析

于2006年4月到2007年8月在泰安市城北设立采样点收集降水样品,对样品中的13种美国环保署(US EPA)优控多环芳烃(PAHs)及NO3-、SO42-等无机阴、阳离子进行了定量分析.测定结果表明,雨水样品中∑13PAHs含量范围在11.3～179.4ng/L之间,平均浓度为89.8ng/L;NO3-、SO42-分别在16.35～186.4ueq/L及53.83～721.9ueq/L之间;样品中无机阴、阳离子总和之比∑(+)/∑(-)的平均值为0.93.相关分析表明,样品中菲、芴、萤蒽等3、4环多环芳烃化合物含量较高;样品中的PAHs浓度与季节存在一定的相关性,但与样品中的NO3-、SO42-浓度间无明显的相关性;样品中的多环芳烃主要来源于煤炭、木材及石油的不完全燃烧.     

土壤和沉积物样品中均三嗪类农药测定相关保存条件探究

采用加速溶剂萃取-高效液相色谱法探究土壤和沉积物中11种均三嗪类农药测定相关保存条件。结果表明,在4℃以下避光、密封,标准贮备液可保存60 d;标准曲线系列溶液可重复使用11 d;阿特拉津等6种化合物的土壤样品可保存20 d,其他化合物可保存5 d~12 d;经过冷冻干燥处理,阿特拉津等7种化合物的沉积物样品可保存8 d,其他化合物可保存12 d;土壤提取液至少可保存60 d。     

顶空固相微萃取-毛细管气相色谱表面发射火焰光度法测定淡水中有机锡化合物

采用固相微萃取(SPME)技术对河水样品中的丁基锡化合物进行富集后直接用气相色谱分离测定.实验中应用了涂层性质和厚度各不相同的商品纤维,也应用了自制的吸附纤维,将所得结果进行比较,发现100μm聚二甲基硅氧烷涂层萃取各丁基锡化合物的灵敏度及重现性均是最好的.将依此为基础建立的SPME-GC-FPD方法用于河水中有机锡化合物的测定,方法非常灵敏和快速.     

GC-C-IRMS测定污染场地土壤中苯系物单体碳同位素比值

选取苯系物中的代表性组分苯、甲苯和二甲苯等化合物,通过热脱附、气相色谱质谱条件的优化及方法学考察,建立了热脱附进样-气相色谱-同位素比值质谱(GC-C-IRMS)测定苯系物单体碳同位素比值的方法。结果表明,单体化合物进样量在0.3μg以上均能满足测定要求;与直接进样方式相比,热脱附进样对单体碳同位素比值测定无分馏影响;标准溶液和苯系物土壤样品测定结果的RSD分别为1.0%~1.7%和0.3%~2.6%。     

直接进样-气相色谱质谱法同时测定固定污染源排气中的含氟温室气体

建立了一种直接进样-气相色谱质谱法同时分离和测定固定污染源排气中三氟甲烷、四氟甲烷、六氟乙烷和六氟化硫等含氟温室气体的方法。使用CP-Sillica PLOT毛细管填充柱可使上述4种目标化合物实现基线分离。分别用全扫描模式和选择离子扫描模式进行定量分析,方法检出限分别为0.12,0.19,0.10,0.08 mg/m~3和2.8,3.4,1.7,3.1μg/m~3。探讨了样品保存容器与保存时间对样品浓度衰减的影响,指出Tedlar采样袋或铝塑复合膜采样袋可以较长时间保存样品,在常温下,样品可保存至少7 d。实际样品测定结果表明方法快速、简便,适用于固定污染源排气中含氟温室气体的测定。     

高效液相色谱-二极管阵列检测器测定邻苯二甲酸酯色谱条件优化

采用高效液相色谱-二极管阵列检测器对6种PAEs类物质进行测定,并对梯度洗脱条件、流速、检测波长等影响化合物色谱响应的关键参数进行优化。综合考虑样品测试效率、分析精度、实际样品中存在杂质干扰等因素,确定以乙腈-水为流动相进行梯度洗脱,洗脱0~11 min流动相乙腈-水梯度比例为50∶50,11 min后流动相调整为100%乙腈,各化合物均能完全分离;色谱分析流速为0.8 m L/min;PAEs的最佳吸收波长为225 nm。在优化的色谱条件下,6种PAEs的线性良好,相关系数均大于0.999 8,仪器检出限为0.08~0.12 mg/L,保留时间、峰面积的相对标准偏差分别为0.02%~0.60%、0.13%~0.86%。方法灵敏度较高,适合土壤等邻苯二甲酸酯含量较高基质样品的快速分析。     

空气中总悬浮颗粒物的X射线衍射定性分析研究

以天津市环境监测中心采集的空气中总悬浮颗粒物（ＴＳＰ）膜（９７１０１２号）为样品，使用日本理学Ｄ／ｍａｘＲＡＸ射线衍射仪对其进行化合物定性分析，并介绍样品的采集与制样方法、仪器测试条件。最后通过ＪＣＰＤＳＩＣＤＤ（国际粉末衍射数据中心）标准数据库检索出该样品所含的全部化合物     

郑州市不同季节空气中醛酮类化合物污染特征及来源

选择郑州市6个特征区域进行布点,在冬季和夏季,每季连续3 d采集样品,并采用2,4-二硝基苯肼吸附管吸附大气样品-高效液相色谱法测定大气中醛酮类化合物浓度水平。结果表明,郑州市大气中主要的醛酮类化合物是甲醛、乙醛、丙酮和2-丁酮,它们的小时平均质量浓度冬季分别为8.23、7.67、13.9、1.56μg/m3,夏季分别为15.4、10.3、17.1、3.30μg/m3,夏季浓度明显高于冬季;无论冬季或夏季昼间浓度均普遍高于夜间,甲醛、乙醛和丙酮的日变化最高质量浓度多出现在08:00~09:00或12:00~13:00或18:00~20:00等时段;甲醛、乙醛和丙酮在冬季相关性较好,具有相同的源和汇,甲醛和乙醛在夏季相关性较好,而甲醛、乙醛和丙酮在夏季的相关性较差。大气醛酮类化合物变化趋势表明,机动车尾气排放和光化学反应是郑州大气醛酮类化合物的重要来源。     

使用保留时间锁定和GC/MS对ppt级的农药进行定性和定量分析

在质谱全扫描模式下典型的农药定量限在亚ppm级范围。使用保留时间锁定气相色谱 /质谱方法 ,选择离子检测 ,实验室可以将目标化合物定量限降低至ppb级 (pg/μl)以下。如在方法中使用大体积进样 ,目标化合物可在ppt级进行定量。专门建立的 5 6 7种化合物的保留时间锁定农药质谱库 ,能够在很短的时间内从采集样品数据文件中自动筛选出这5 6 7种化合物。谱库也可以用于选择离子检测方法采集样品的快速筛选。使用化合物谱库信息 ,可以在 2小时之内建立一个包括 80种目标化合物的选择离子检测方法 ,而不需运行任何分析过程     

吹扫捕集气相色谱质谱法测定土壤中挥发性有机物

建立了吹扫捕集气相色谱质谱法同时测定土壤中卤代烃类、苯系物类、氯代苯类等二十多种挥发性有机物.使用模拟土壤和实际土壤样品优化了吹扫时间、吹扫温度等参数;采用内标法绘制了校正曲线,各目标化合物5个浓度水平的响应因子的相对标准偏差均小于20%,相关系数均大于0.999;测定了方法检出限,采用2g土壤,各目标化合物方法检出限界于0.02～1.00μg/kg;对两种总有机碳含量的实际土壤样品进行了加标回收实验,回收率范围64%～123%.     

乌鲁木齐市汽车尾气污染状况调查

对乌鲁木齐市主要街道受汽车尾气污染的调查和综合分析得到CO、NOx、HC的污染规律,主要街道路中心空气中CO、NOx日均值已超出国家大气环境质量二级标准,市区主要街道的人行道空气中NOx含量已超出二级标准,Ⅱ、Ⅲ类道路人行道空气中CO含量已超标;在三类街道中,Ⅰ类街道车流量最大,Ⅱ类次之,Ⅲ类最少,而汽车排放尾气对街道空气污染状况为Ⅲ类最重、Ⅱ类次之、Ⅰ类最轻。     

Gross alpha and beta radioactivity concentration in water, soil and sediment of the Bendimahi River and Van Lake (Turkey)

The concentrations of the natural radioactivity in water, soil and sediment samples collected from Bendimahi River which originates near the Tendürek Mountain (Van, Turkey), its tributaries and Van Lake (Turkey) were measured. The gross-alpha and gross-beta radioactivity concentrations were investigated in May and August in 2005. Determination of the gross-alpha and gross-beta radioactivity of river water, soil and sediment samples was obtained by using gas-flow proportional counter, PIC-MPC 9604-alpha/beta counter. In water samples, the obtained results show that in May; gross-alpha and gross-beta activity concentrations varied between 0.063-0.782 and 0.021-0.816 Bq l(-1) and in August the values were 0.009-0.037 and 0.081-3.116 Bq l(-1), respectively. The gross-alpha and gross-beta activity concentrations in soil samples ranged from 0.800 to 4.277 Bq g(-1) and 0.951 to 11.773 Bq g(-1) in May and 0.686 to 4.713 Bq g(-1) and 0.073 to 9.524 Bq g(-1) in August, respectively. Concentrations ranging from 0.782 to 4.596 Bq g(-1) and from 0.482 to 10.372 Bq g(-1) in May and from 0.580 to 5.824 Bq g(-1) and from 0.303 to 9.702 Bq g(-1) in August for gross-alpha and gross-beta radioactivity were observed in sediments, respectively.     

Dispersion in Urban Environments; Comparison of Field Measurements with Wind Tunnel Results

A wind tunnel study was performed to determine the dispersion characteristics of vehicle exhaust gases within the urban canopy layer. The results were compared with those from a field monitoring station located in a street canyon with heavy traffic load. The agreement found was fair. In the second part of the paper it is shown how wind tunnel data can be utilized to supplement and thereby enhance the value of field data for model validation purposes. Uncertainty ranges were quantified which are inherent to mean concentration values measured in urban streets.     

Seasonal variation of nonylphenol concentrations and fluxes with influence of flooding in the Daliao River Estuary, China

Nonylphenol is an endocrine disruptor with harmful effects including feminization and carcinogenesis on various organisms. This study aims to investigate the distribution and ecological risks of nonylphenol in the Daliao River Estuary, China. Nonylphenol, together with other phenolic endocrine disruptors (bisphenol A, 4-t-butylphenol, 4-t-octylphenol, and 2,4-dichlorophenol), was detected in surface water and sediment on three cruises in May 2009, June 2010, and August 2010, respectively. A large flooding occurred during our sampling campaign in August and its effect on nonylphenol concentrations and fluxes in the estuary was therefore evaluated. The results showed that nonylphenol with a concentration range between 83.6–777 ng l^?1 and 1.5–456 ng?g^?1 dw in surface water and sediment was the most abundant among the phenolic compounds, accounting for 59.1–81.0 and 79.9–92.1 % of the total phenolic concentration in surface water and sediment, respectively. The concentrations recorded in May and June were comparable, whereas those in August were considerably higher, mainly due to the flush of flooding. The flooding also caused a 50 times increase in nonylphenol flux from the estuary into the adjacent Bohai Sea. Nonylphenol concentrations in the estuary have exceeded the threshold level of undesirable effects with a potential risk of harm to local species, especially benthic organisms.     

荆门市近十年大气降雨的变化特征分析

利用荆门市2001—2010年对城区和石化区的降水监测资料,研究分析了荆门市近十年来的大气降水量、pH及电导率的变化情况。结果表明:荆门市近十年来的年均降水量为793.27 mm,降水主要集中在5—8月,年降水量变化较大,基本呈周期性的波动趋势。荆门市城区降水的pH和电导率比较稳定,没有出现酸雨。石化区的降水年平均pH比城区低,年平均电导率比城区高,有酸雨发生,但污染并不严重。     

An assessment of air quality in Karachi,Pakistan

An atmospheric pollution survey was carried out at 13 sites in Karachi, Pakistan, simultaneously from 0600 h to 2100 h for 15 consecutive days in May 1990 which also included meteorological measurements. The monitoring sites were included along the prevailing wind patterns in Karachi. Carbon monoxide levels in the ambient air were found to reach 9–10 ppm along the busy urban streets whereas CO₂ level exceeded 370 ppm in these areas. Our survey indicates that NO₂ levels were exceeding U.S. ambient air quality standards. Maxmum NO₂ concentrations were observed (0.3–0.5 ppm) during the daytime from 0600 h to 2100 h. The surface ozone maximum around noon at the inland sites reached the levels of 40 ppb and 50 ppb respectively compared to upwind coastal Sites 1 level of 25 ppb. The Pb concentrations were approximately 3- to 7-fold higher than average, which corresponded well to urban air. Fossil fuel SO₄ (excess) and NO₃ were apportionally based on the assumption that these two anions were present as (NH₄)₂SO₄, and NH₄NO₃ in the aerosols. In the eastern part of the city atmospheric sulphate (SO₄) shows the combustion of coal as its source from the vicinity and downwind of a steel manufacturing plant.     

Traffic-generated noise pollution: exposure of road users and populations in Metropolitan Kuwait

This study was carried out in metropolitan Kuwait with a sound level meter to assess peak hour and off-peak hour noise level. In local/collector streets, noise ranged between 56.0 to 79.2 dBA and 55.3 to 76.4 dBA; in arterial streets, 62.3 to 89.2 dBA and 59.6 to 78.9 dBA; and in freeways, 66.7 to 94.8 dBA and 64.9 to 89.1 dBA during peak and off-peak hour respectively. Values were higher than their prescribed standards which may pose a significant impact on quality of life. Findings of this research have shown that the level of traffic-generated noise pollution in Kuwait urban area is high enough to adversely affect the human health and well-being of its residents. Over 1,400 subjects responded to a randomly administered survey that assessed the physical health, personal well-being, and mental health. People residing in neighborhoods exposed to higher noise levels have significantly higher stress and noise annoyance levels and also adversely affected their sense of well-being. In the responder analysis, those people living in quiet neighborhoods had significantly higher mean scores in general health (35 points higher, p < 0.05), sense of vitality (30 points higher, p < 0.05), and mental health (20 points higher, p < 0.05) when compared to the other group. In addition, the component scores of stress and noise sensitivity for the participants living in quiet neighborhoods had significantly lower values (30 points lower and 59 points lower, respectively) than that of the participants living in noisy neighborhood. With the rapid expansion of the infrastructures in metropolitan Kuwait, it is virtually definite that traffic noise will shortly assume a dangerous dimension, and will be a ground of escalating fear for both the public and liable policy-makers. The quality of life in metropolitan Kuwait will certainly be negatively affected.     

Can NO(2) be used to indicate ambient and personal levels of benzene and 1,3-butadiene in air?

The aim of this study was to investigate the relation between two toxic volatile organic compounds, 1,3-butadiene and benzene, and a commonly used indicator of vehicle exhaust fumes, NO(2). This was to see if NO(2) can be used to indicate personal exposure to carcinogenic substances or at least estimate ambient levels measured at a stationary point. During the winter of 2001, 40 randomly selected persons living in the City of Umea (in the north of Sweden) were recruited to the study. Personal measurements of 1,3-butadiene, benzene and NO(2) were performed for one week, and were repeated for 20 of the 40 participants. Additional information was gathered using a diary kept by each participant. During the same time period weekly stationary measurements were performed at one urban background station and one street station in the city centre. The results from the personal measurements showed a negligible association of NO(2) with 1,3-butadiene (r= 0.06) as well as with benzene (r= 0.10), while the correlation coefficient between 1,3-butadiene and benzene was high and significant (r= 0.67). In contrast to the personal measurements, the stationary measurements showed strong relations between 1,3-butadiene, benzene and NO(2) both within and in-between the street and urban background station. This study supports NO(2) as a potential indicator for 1,3-butadiene and benzene levels in streets or urban background air, while the weak relations found for the personal measurements do not support the use of NO(2) as an indicator for personal 1,3-butadiene and benzene exposure.     

Assessment of some trace heavy metals and radioactivity concentration in water of Bendimahi River Basin (Van, Turkey)

The levels of heavy metals were determined in the water of Bendimahi River Basin, statistically analysed and compared to natural gross radioactivity concentration. Fifteen samples of water were collected from Bendimahi River and Van Lake for two seasons in 2005. Water samples were analyzed for eight trace elements and concluded together with gross-alpha and gross-beta radioactivity concentrations. Atomic absorption spectrometry (AAS) was used to determine the concentrations of heavy metals in water samples collected from Bendimahi River basin. Correlation analysis was made for radioactivity and heavy metal concentrations and the Pearson correlation coefficients between gross-alpha and gross-beta radioactivity and heavy metal were determined. The concentrations of all metals were found to be higher than WHO, EC, EPA and TSE-266 guidelines for drinking water, except for Zn and Cu. Generally, the heavy metal concentrations in water samples obtained in May and in August were found to be in sequence of Fe>Zn>Pb>Cr>Cu>Mn>Co>Cd and Fe>Zn>Cu>Pb>Cr>Mn>Co>Cd, respectively. The gross-alpha and gross-beta activity concentration varies between 0.063 and 0.782, 0.021 and 0.816 Bq l(-1) in samples collected in May, and 0.009 and 0.037, 0.081 and 3.116 Bq l(-1) in samples collected in August.     

广州不同环境空气PM2.5中金属元素污染特征与风险评价

根据2015年广州城区磨碟沙、内陆郊区天湖和近海郊区万顷沙不同环境空气PM_2.5中金属元素（Pb、Cd、Cr、Ni、As等23种）监测数据，分析其污染特征与富集程度，并评估潜在生态风险和健康风险，为大气污染风险防控提供支持。结果显示：广州大气PM_2.5中金属K、Na、Fe、Ca、Al和Zn含量相对较高。总元素浓度总体呈冬季最高、夏季最低的特征，且随PM_2.5污染加重而升高，但总元素在PM_2.5中的占比下降。Cd、Se、Zn、Cu、Mo、Pb和Na富集严重（富集因子>100），体现了人类活动的重要影响，磨碟沙城区站富集因子通常高于另2个站点。广州大气总金属元素潜在生态危害程度为"很强"，Cd贡献为主，Pb、Cu和As元素贡献分别在天湖、磨碟沙和万顷沙位列第二。As、Cr和Mn是大气金属元素健康风险的主要贡献者；磨碟沙的总致癌效应风险高于万顷沙和天湖，但万顷沙的总非致癌效应风险最高。