汽车修理养护企业挥发性有机物排放控制标准探讨

通过对汽车修理养护企业喷烤漆废气排放现状进行调查分析,指出中国目前适用于控制汽车修理养护企业废气排放的标准《大气污染物综合排放标准》(GB 16297-1996)在实际运用中存在的问题。依据《制定地方大气污染物排放标准的技术方法》(GB/T 3840-1991)《大气污染物综合排放标准详解》《工作场所有害因素职业接触限值化学有害因素》(GBZ 2.1-2007)《工业企业设计卫生标准》(TJ 36-1979)、美国环保局多介质环境模型等,用不同方法计算汽车修理养护企业排放的废气中几种挥发性有机物的排放浓度和排放速率限值,并对监测结果进行评价分析,提出编制汽车修理养护企业废气排放控制标准的建议。     

定型机油烟废气监测分析方法初探

定型机废气污染是当前环境投诉的热点之一,油烟污染是定型机废气的主要问题,我国尚无定型机废气监测分析的标准方法。本文参照《餐饮业油烟排放标准》（试行）（GB 18483-2001）中的方法,比较了餐饮业油烟废气和定型机油烟废气在成分、排放方式等方面的相同点和不同点,从采样方法、采样时间等对定型机油烟废气的监测分析进行了初探,确定了定型机油烟废气竣工验收参考的采样方法和时间等要素。     

铬盐工业项目特征污染物的监测与数据问题分析

对铬及其化合物工业项目排放废气中特征污染物的监测方法和评价标准问题进行探讨,提出了验收监测应参考《大气污染物综合排放标准》(GB 16297—1996)的建议;通过对监测数据的合理性和逻辑性分析,提出了现场监测和数据审核的注意事项,应严格监控工况,并详细记录关键设备运行参数;提出应把废气中六价铬作为特征污染物控制指标,并结合新颁布的《环境空气质量标准》(GB 3095—2012)中对六价铬的要求,确定合理的排放限值,并研究适合的配套监测方法,为后续铬及其化合物工业污染物排放标准以及特征污染物监测方法的制修订提供技术依据。     

烟气连续监测系统的相对准确度检测

阐述了HJ／T76—2001《固定污染源排放烟气连续监测系统技术要求及检测方法》标准中烟气连续监测系统的相对准确度计算和相对准确度计算中存在的问题。对存在问题中的重复性或复现性的假设、B类不确定度的忽略、标准分析方法平均值的采用和偏差检验进行了探讨。     

生活垃圾焚烧炉烟气新标准可达性分析

对《生活垃圾焚烧污染控制标准》(GB 18485—2001)和《生活垃圾焚烧污染控制标准》(GB 18485—2014)中各项指标的排放限值作比较,并探讨了二噁英、重金属、酸性气体、烟尘、碳氧化物等烟气污染物的控制措施。结合2010—2014年浙江省部分生活垃圾焚烧厂"三同时"验收废气监测数据,对排放指标的达标情况作分析,结果表明,采用"3T+E"焚烧工艺+SNCR脱硝+半干法脱酸+活性炭喷射+布袋除尘器除尘的烟气污染控制技术,可以同时满足脱氮、脱酸、除尘,以及去除重金属和二噁英的要求。     

沥青烟中苯并(a)芘的等速采样与监测

新的大气污染综合排放标准对沥青及碳素制品生产和加工制定了沥青烟和苯并(a)芘的排放标准,然而空气和废气监测分析方法没有给出沥青烟气中苯并(a)芘的分析方法.为此,用色谱固定液滤筒及新设计的富集器等速采样,进行沥青烟苯并(a)芘的分析,为执行新的大气污染综合排放标准提供了实用技术.     

浸渍滤膜采样——氟离子选择电极测定废气中氟化物

废气中氟化物的测定,通常采用碱液吸收——氟离子选择电极测定的方法.该方法分析部分具有快速、灵敏、适用范围宽、方法简便、准确、选择性好等优点.但现场采样部分较繁琐,不适用于根据GBJ4—3排放标准设计的排放浓度(1～10)毫克/米~3范围内氟化物的测定.本文采用《空气和废气监测分析方法》(以下简称《方法》)介绍的碳酸氢钠甘油浸渍滤膜——氟离子选择电极测定空气中氟化物的方法,对废气中氟化物含量进行测定,得到了满意的结果.     

测定环境空气中砷及其化合物的方法改进

对《空气和废气监测分析方法》中砷的采样和测定方法进行了改进,并在云南某炼铜厂环境空气中含砷监测进行了实际验证。结果表明,方法的检出限、精密度、准确度均能满足测定的要求,并且更适合测定高浓度砷。     

杭州市燃煤废气中重金属排放清单建立

采用基于燃料消耗的排放因子法,以污染源普查动态更新数据为基础,建立了2010年杭州市燃煤废气中重金属(汞、砷、铅、镉、总铬、镍、锑等7种)排放清单。结果表明,2010年杭州市燃煤废气中汞、砷、铅、镉、总铬、镍、锑的年排放量分别为194.2、252.9、1 915.7、53.9、3 390.4、1 465.4、101.0 kg。燃煤废气中重金属的排放主要集中在燃煤消耗较高的拱墅区和江干区,其次是上城区,这3个区燃煤废气中重金属的排放量之和超过全市的95%。燃煤废气中重金属的排放量与燃煤量密切相关,但锅炉燃烧方式、除尘脱硫设施对重金属排放也起到了决定性作用。     

生活垃圾焚烧烟气中重金属排放水平及影响因素分析

通过对浙江省生活垃圾焚烧炉排放烟气中重金属的监测,分析生活垃圾焚烧烟气中重金属排放水平。结果表明,汞及其化合物的检出率最高,为95.7%,其次为铬和锰,检出率均为60%,且在不同的焚烧炉中重金属排放浓度差异较大,检出率最低的为铊和镉,且排放浓度均较低;焚烧炉排放烟气中汞及其化合物、镉+铊及其化合物、锑+砷+铅+铬+钴+铜+锰+镍及其化合物排放浓度均低于国标排放限值,最大占标率分别为76%、4%、21.9%。焚烧烟气中的重金属含量与焚烧垃圾中的重金属含量有关,烟气通过废气处理设施,可有效地减少重金属等污染物的排放。     

Arsenic exposure in Hungary, Romania and Slovakia

Inorganic arsenic is a potent human carcinogen and toxicant which people are exposed to mainly via drinking water and food. The objective of the present study was to assess current exposure to arsenic via drinking water in three European countries. For this purpose, 520 individuals from four Hungarian, two Slovakian and two Romanian countries were investigated by measuring inorganic arsenic and methylated arsenic metabolites in urine by high performance liquid chromatography with hydride generation and inductively coupled plasma mass spectrometry. Arsenic in drinking water was determined by atomic absorption spectrometry. Significantly higher concentrations of arsenic were found in both the water and the urine samples from the Hungarian counties (median: 11 and 15 microg dm(-3), respectively; p < 0.001) than from the Slovakian (median: 0.94 and 4.5 microg dm(-3), respectively) and Romanian (median: 0.70 and 2.1 microg dm(-3), respectively) counties. A significant correlation was seen between arsenic in water and arsenic in urine (R(2)= 0.46). At low water arsenic concentrations, the relative amount of dimethylarsinic acid (DMA) in urine was increased, indicating exposure via food. Also, high body mass index was associated with higher concentrations of arsenic in urine (p= 0.03), mostly in the form of DMA. Smokers had significantly higher urinary arsenic concentrations than non-smokers (p= 0.03). In conclusion, elevated arsenic exposure via drinking water was prevalent in some of the counties. Exposure to arsenic from food, mainly as DMA, and cigarette smoke, mainly as inorganic arsenic, are major determinants of arsenic exposure at very low concentrations of arsenic in drinking water.     

Arsenic transformations in terrestrial small mammal food chains from contaminated sites in Canada

Arsenic in terrestrial contaminated sites has the potential to cause harm to residential wildlife. The aim of this study was to determine the arsenic species in wild rodents living in arsenic contaminated habitats, specifically deer mice from Yellowknife, NT and meadow voles from Seal Harbour, NS, along with co-located plants. Methanol : water (1 : 1) extractions were used to optimize the extraction of methylated arsenic(v) species. Total arsenic concentrations were substantially higher in the Yellowknife deer mice (1.7-3.2 μg kg(-1) wet weight in livers) and Seal Harbour meadow voles (0.67-0.97 μg kg(-1) wet weight in livers) living on the contaminated sites with respect to the surrounding background locations (0.12-0.34 μg kg(-1) wet weight in livers). Around 50% of arsenic could be identified in Yellowknife deer mouse tissues, but only <10% was identified in Seal Harbour vole tissues; inorganic arsenic (iii and v) and dimethylarsinic acid were all found. Monomethylarsonic acid was only detected in both the mice and voles living in the contaminated sites. In the Yellowknife food chain, methyl arsenic (v) proportions increased from plants to mouse inner organs, but the trend was not for clear as the Seal Harbour food chain. Seal Harbour voles may be sequestering arsenic in a less mobile form, rather than transforming it.     

微波消解-原子荧光法测定环境空气中的砷

建立了浸渍滤膜吸附-微波消解-原子荧光法测定环境空气中的砷的方法，改进了原有的采样方法，有效地克服了原方法中湿法消解的缺点，并大大降低了检出限，能够满足《环境空气质量标准》（GB3095—2012）中对砷排放的参考浓度限值要求。     

Arsenic contamination and speciation in surrounding waters of three old cinnabar mines

The impact of arsenic pollution in waters from the surroundings of three abandoned Hg mines in Northern Spain, as well as reaching the Caudal River, was evaluated. For assessing the factors controlling arsenic release, an extensive study based on the physicochemical characterization and multivariate statistical analysis of waters upstream and downstream each mine site was performed. Waters downstream of the La Soterra?a mine present the highest arsenic concentrations, up to 38.8 mg L(-1), coming mainly from the solubilisation of calcium, magnesium and strontium arsenates at a pH close to neutral. Although arsenic concentrations downstream of La Pe?a are markedly lower, these values remain too high, indicating that the encapsulation carried out in this spoil heap is insufficient. In addition, the high water flow in this point involves an extremely high input of arsenic to the surroundings (0.3 g s(-1)). Waters close to tailings from Los Rueldos suffer from acid mine drainage, provoking an important solubilisation of arsenic and heavy metals, a situation which is rapidly softened with distance. The study of arsenic speciation reveals the omnipresence of As(v) in waters from the three mines, whereas in La Pe?a low amounts of As(iii) were also detected. Different preservation methods for As speciation were compared, such as the addition of HCl, EDTA and the storage of samples without any additive, and no alteration of samples in any case up to nine months after the collection was observed. A study of seasonal variations of As and the main parameters affecting its concentration and speciation was completed throughout a year, showing no remarkable dependency with rainfall for any studied variable.     

高效液相色谱-原子荧光光谱联用分析土壤中形态砷

采用高效液相色谱(HPLC)-原子荧光光谱(AFS)联用技术分析土壤中亚砷酸盐[As(Ⅲ)]、二甲基砷(DMA)、一甲基砷(MMA)和砷酸盐[As(Ⅴ)]等4种形态砷,以磷酸为提取剂、抗坏血酸为还原剂,优化了水浴提取条件。As(Ⅲ)、DMA、MMA和As(Ⅴ)在7 min之内实现了完全分离,在1.00μg/L～100μg/L范围内线性良好,实验室检出限分别为0.25μg/L、0.36μg/L、0.39μg/L和0.51μg/L,土壤标准样品平行测定的RSD≤7.4%,加标回收率为79.5%～95.0%,提取率为74.6%～90.4%。     

双道原子荧光同时测定海水中痕量砷和汞

建立了双道原子荧光同时测定海水中痕量砷和汞的方法。在试验条件下,砷和汞测定的相对标准偏差≤4．0％．加标回收率在92．0％～104％之间。方法操作简便,灵敏快速,适用于海水及其他水体中砷和汞的测定。     

Arsenic speciation in human hair: a new perspective for epidemiological assessment in chronic arsenicism

The analysis for arsenic in hair is commonly used in epidemiological studies to assess exposure to this toxic element. However, poor correlation between total arsenic concentration in hair and water sources have been found in previous studies. Exclusive determination of endogenous arsenic in the hair, excluding external contamination has become an analytical challenge. Arsenic speciation in hair appears as a new possibility for analytical assessing in As-exposure studies. This study applied a relative simple method for arsenic speciation in human hair based on water extraction and HPLC-HG-ICP-MS. The concentration of arsenic species in human hair was assessed in chronically As(V)-exposed populations from two villages (Esqui?a and Illapata) of the Atacama Desert, Chile. The arsenic concentrations in drinking water are 0.075 and 1.25 mg L(-1), respectively, where As(V) represented between 92 and 99.5% of the total arsenic of the consumed waters. On average, the total arsenic concentrations in hair from individuals of Esqui?a and Illapata were 0.7 and 6.1 microg g(-1), respectively. Four arsenic species, As(III), DMA(V), MMA(V) and As(V), were detected and quantified in the hair extracts. Assuming the found species in extracts represent the species in hair, more than 98% of the total arsenic in hair corresponded to inorganic As. On average, As(III) concentrations in hair were 0.25 and 3.75 microg g(-1) in Esqui?a and Illapata, respectively; while, the As(V) average concentrations were 0.15 and 0.45 microg g(-1) in Esqui?a and Illapata, respectively. Methylated species represent less than 2% of the extracted As (DMA(V)+ MMA(V)) in both populations. As(III) in hair shows the best correlation with chronic exposure to As(V) in comparison to other species and total arsenic. In fact, concentrations of As(total), As(III) and As(V) in hair samples are correlated with the age of the exposed individuals from Illapata (R= 0.65, 0.69, 0.57, respectively) and with the time of residence in this village (R= 0.54, 0.71 and 0.58, respectively).     

Arsenic concentration and speciation of the marine hyperaccumulator whelk Buccinum undatum collected in coastal waters of Northern Britain

European whelks (Buccinum undatum) have shown to accumulate high levels of arsenic. Since the accumulation process is not well understood it is necessary to gain information about the geographical variability of the arsenic concentration in them. Here we show that the mean arsenic concentrations of the whelks are site specific and vary by a factor of 3.5 in ten different geographical locations. At fishing grounds where whelks exhibited low arsenic concentrations the arsenic concentration increased linearly with size, whereas the whelks with high arsenic levels from a different location showed no correlation. Although the overall arsenic concentration in the whelks differed between 45 and 655 mg kg(-1) d.w., the inorganic arsenic concentration did not exceed 0.4 mg kg(-1) d.w. The main arsenic compound is arsenobetaine, which is widely considered as non-toxic. The exposure to toxic inorganic arsenic when eating whelks cannot be estimated from their size or their total arsenic concentration.     

微波消解-氢化物发生原子荧光光度法 测定土壤中的砷

建立了微波消解一氢化物发生原子荧光光度法测定土壤中砷的方法。对微波消解条件进行了优化，用5mL硝酸和2mL过氧化氢的混合酸作消解溶剂，在设定的微波条件下砷提取完全。用5％的盐酸作为反应载流，12g／L硼氢化钾与0．5％氢氧化钠的混合液为还原剂，直接定容后应用HG．AFS测定，并通过测定国家标准参考物质和加标回收实验，对方法进行了验证。实际土壤加标同收率97％～103％。