Teil 3: PCDD/F im Blutfett ausgewählter Personen

This study was designed to assess the degree of exposure to PCDD/F in 56 selected persons living in the vicinity of a former copper smelter located in Marsberg, Germany. The copper smelter was in operation until 1945. In 1991, high levels of PCDD/F were found particularly in materials from the slag dumps (10 000 – 100 000 ng TE/kg). The levels of PCDD/F in blood fat were used as parameters for individual PCDD/F exposure. Since only limited reference data for PCDD/F in human blood were available, blood samples of a reference group were analyzed in the same way. The criteria were collected from a group matched for sex, age (±3 years) and body mass. The median NATO/CCMS-Toxicity equivalency values (NATO/CCMS-TE-values) of the Marsberg group (43,2 pg NATO/CCMS-TE/g blood fat) and the reference group (43,0 pg NATO/CCMS-TE/g blood fat) were similar, whereas the arithmetic mean of the Marsberg group (52,7 pg NATO/CCMS-TE/g blood fat) was higher than that of the reference group (44,4 pg NATO/CCMS-TE/g blood fat). The frequency distribution of the individual TE-values of the Marsberg group was slightly shifted toward higher values. The individuals of the Marsberg group had significantly higher levels of PentaCDF, HexaCDF and HeptaCDF on average than the individuals of the reference group. On the basis of TE-values, the majority of the individuals from Marsberg did not have an increased body burden of PCDD/F. However, some individuals could be identified with TE-values exceeding background levels ranging up to 231 pg NATO/CCMS-TE/g blood fat. Although it must be assumed that the unusual congener pattern found in many of the test subjects is a result of ingestion of contaminated slag material or soil, the findings of this study could not verify this fact.     

Teil 1: PCDD/F in Böden,Vegetation und Kuhmilch

Soil samples were taken from residential gardens, grasslands and forests at 22 locations in Marsberg, North Rhine-Westphalia, and analyzed for PCDD/F. Sampling was concentrated on the vicinity of a former copper smelter where copper waste material (calledKieselrot) was deposited and emissions from former stacks contaminated a large land area. Maximum PCDD/F-concentrations were 407 ng TE GBA/kg dm in garden soil (0–30 cm depth), 98 ng TE BGA/kg dm in agricultural grassland (0–10 cm depth), 227 ng TE BGA/kg dm in wasteland, and up to 8073 ng TE BGA/kg dm in forest soils. PCDD/F-levels in soil decreased with increasing distance from the former sources providing a large historic emission problem, apart from the still existing kieselrot waste site. Ash residues from former flue gas duct showed up to 2,4 mg TE BGA/kg dm. PCDD/F-concentrations in vegetable samples from highly contaminated garden soils and grass from agricultural grassland were found to be relatively low in relation to soil values. PCDD/F-levels in salad showed a mean of 2,2 ng TE BGA/kg dm while grass concentrations were <6 ng TE BGA/kg dm. Thus, no correlation was found between soil and vegetation values with the exception for carrot roots where obviously a small transfer of PCDD/F between the two media took place. PCDD/F-content in grass taken over the vegetation period showed a tendency to increase toward the end of the growing season, which is probably related to changes in the dry matter yield over the season. No correlation was found in general between soil, grass and milk PCDD/F contents when all samples were taken from the same grassland. PCDD/F-concentrations in milk ranged between 0,6 and 1,1 pg TE BGA/g milkfat and were thus in the same range as consumer milk in the Federal Republic of Germany. PCDD/F in needles from conifers showed a clear relationship with respect to distance from the former waste site. The relatively high levels in conifer needles [36 ng TE BGA/kg dm] were obviously due to sporting activities (i.e. motocross racing where contaminated material was resuspended and deposited on surrounding trees).     

Pollution characteristics and potential health risk of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in soil/sediment from Baiyin City, North West, China

In order to better understand the environmental behaviors of persistent organic pollutants, the characteristics of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were investigated in twenty-three soil/sediment samples from Baiying City, Northwest China, in 2008. The possible sources and potential health risk of PCDD/Fs were also discussed. The concentrations of PCDD/Fs in nineteen soil samples varied between 20.13 and 496.26 pg/g dry weight (dw.), with an average value of 125.59 pg/g dw. The highest International Toxic Equivalent (I-TEQ) of PCDD/Fs (8.34 pg/g dw.) in soil was found at sample S1 collected from proximity to a copper metallurgy plant. The concentrations of PCDD/Fs in four sediment samples ranged from 37.69 to 491.49 pg/g dw., with an average value of 169.95 pg/g dw. The highest I-TEQ of PCDD/Fs (8.56 pg/g dw.) in sediment was found at sample S12 collected from the East big ditch with waste water discharged into the Yellow River. The results indicated that PCDD/Fs contamination of soil/sediment is originated from three sources: chlorine-containing chemicals, non-ferrous metal industrial PCDD/Fs emission and coal burning. The health risk exposure to PCDD/Fs through soil, dust ingestion and dermal absorption ranged from 0.0006 to 0.0134 pg/kg/day Word Health Organization’s toxic equivalent in 1998 (WHO₁₉₉₈-TEQ) with mean values 0.0032 pg WHO₁₉₉₈-TEQ for adults and varied between 0.0012 and 0.0256 pg/kg/day WHO₁₉₉₈-TEQ with mean values 0.006 pg/kg/day WHO₁₉₉₈-TEQ for children, respectively. These results indicated that health risk of PCDD/Fs for children should be paid more attention.     

Thermische Schlammkonditionierung nach dem Porteous-Verfahren

In Nuremberg (Germany), each year about 25,000 tons (dry matter) of sewage sludge are obtained as by-product of waste water treatment. The digested sludge consists of 96% water. Until 1992 it was thermally stabilized using the Porteous procedure: the sludge was heated in an autoclave up to a temperature of 180–200 °C at a pressure of 28 bar. After pressure reduction and moving to a thickener, a substantial part of the liquid could be removed. After running through a chamber filter, the sludge contained only about 50% dry matter. This treatment does not only remove water; organic matter is also degraded or evaporated. Between November 1991 and May 1992, the sludge was analyzed four times before and after the drying process and examined for heavy metals (Pb, Cd, Cr, Cu, Ni, Hg, Zn), polychlorinated biphenyls (PCB) and PCDD/F. The concentration of heavy metals and PCB (related to dry matter) increased by a faktor of 1.3 after the drying process. This effect may be explained by the decrease of organic matter during drying. In the case of PCDD/F, the ITQ increased by a factor of 3.2, for some congeners even by a factor of 8. The only explanation can be that during thermal conditioning PCDD/F is formed by precursors as chlorophenols. This formation is probably catalyzed by metals as copper or nickel and sped up by the higher temperatures.     

不同垃圾焚烧炉产生的PCDD/Fs和PCBs同类物的分布

要应用高分辨气相色谱一质谱联用技术，测定了3种垃圾焚烧炉产生的飞灰中17种PCDD／Fs和12种共平面PCBs的浓度及毒性当量，比较了PCDD／Fs和PCBs同类物分布的差异．结果表明，流化床焚烧炉和炉排焚烧炉产生的PCDD／Fs多于PCBs，而气化熔融焚烧炉产生的PCBs多于PCDD／Fs；产生的PCBs对总毒性当量的贡献都比较小；3种焚烧炉产生的PCDD／Fs同类物具有相似的浓度分布；流化床焚烧炉和炉排焚烧炉产生的PCBs同类物具有相似的浓度分布，而气化熔融焚烧炉产生的PCBs同类物分布与其他两种焚烧炉差别较大．     

Polychlorierte Dibenzo-p-dioxine und Dibenzofurane (PCDD/F)

Distillation residues of dry cleaning machines contain small quantities of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/F), independent of the type of solvent employed. PCDD/F were not only detectable in distillation residues using perchloroethylene as dry cleaning solvent, but also similar quantities and congeneric patterns of PCDD/F were found in residues from machines operated with stoddart solvent or CFC 113. Current results suggest that PCDD/F occurrence is linked to the dirt adhering to the textiles. Dirty textiles were a prerequisite for finding PCDD/F in the distillation residues. The congeneric patterns of the identified PCDD/F in the distillation residues were found to be similar as those from household dust, sewage sludge, as well as those from soil, sediments, and street dust. The investigations clearly show that perchloroethylene is not linked to PCDD/F formation. The freshly produced, commercial perchloroethylene as well as laboratory-distilled perchloroethylene did not contain any detectable quantities of PCDD/F. Also, the possibility of PCDD/F formation through decomposition reactions of the solvents during the dry cleaning process can be excluded on the basis of existing data.     

Spatial distribution of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in soil around a municipal solid waste incinerator

Municipal solid waste incinerators (MSWIs) are usually considered to be important sources of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs). To examine the influence of PCDD/Fs emissions from a MSWI on the surrounding environment, 21 soil samples were collected from various sampling sites distributed at distances of 300–1,700 m away from the stack of a MSWI. International Toxic Equivalent (I-TEQ) concentrations ranged from 0.47 to 2.07 pg I-TEQ g^?1, with average and median concentrations of 1.08 and 1.05 pg I-TEQ g^?1, respectively. Comparison of the results presented herein with other worldwide studies suggested that the concentrations of PCDD/Fs in the ambient soil were relatively low, indicating a limited impact on the surrounding environment. The emission concentrations from the incinerator were the critical factor in generating an environmental impact on the surrounding environment. An exponential function was developed, indicating a slight decline in TEQs of PCDD/Fs with increasing distance from the MSWI stack. The ordinary kriging interpolation technique was selected to create a contour map, which intuitively showed that a limited surrounding area (≤1,000 m from the stack) was obviously influenced by the MSWI.     

PCDD/DFs and coplanar PCBs in fly ash samples from various types of incinerators in Taiwan

Polychlorinated dibenzo‐p‐dioxins and dibenzofurans (PCDD/DFs) and coplanar polychlorinated biphenyls (Co‐PCBs) were determined in fly ash samples from municipal solid waste (MSW), medical waste (MW), and electricity power plant incinerators in Taiwan. The average concentrations of PCDD/DFs and Co‐PCBs are 7.02 ng‐TEQ/g and 1.06 ng‐TEQ/g, respectively. The contributions to total TEQ are 24% from PCDDs, 64% from PCDFs, and 12% from Co‐PCBs, indicating that PCDFs generate the highest environmental impact and MSW and MW incinerators are potential Co‐PCBs contaminating sources. The levels of PCDD/DFs and Co‐PCBs found in ash samples increase from petroleum‐fired, coal‐fired, large municipal solid waste, small medical waste, to small municipal solid waste incinerators, and are generally lower than those from incinerators built earlier. All fly ash samples analyzed in this study were considered hazardous materials. More research is suggested to establish the relationship between the amounts of PCDD/DFs and Co‐PCBs in fly ash and in flue gas.     

利用EIA法快速筛查垃圾焚烧飞灰和烟气中的二恶英毒性水平

基于CAPE技术公司的兔子复合克隆抗体的二恶英(PCDD/F)酶免疫分析试剂盒,建立了快速检测垃圾焚烧飞灰和烟气中PCDD/F毒性(TEQ值)的方法.试剂盒的最低检测限为3.3pg·tube-1(即3.3pgTEQ每EIA试管),线性检测范围为10～30pg·tube-1.样品经甲苯索氏抽提后过硅胶柱连接小碳柱净化处理,TCDD/F的回收率大约为50%,与原飞灰PCDD/F分布模式相比净化处理后样品中的TCDD/F含量明显降低.用净化处理后的飞灰溶液作标准溶液,绘制PCDD/F剂量-效应关系曲线,定量分析了2个飞灰样品和2个烟气样品的TEQ浓度,结果表明分析样品的TEQ实测值(HRGC/HRMS分析获得)与预测值(标准曲线计算值)的相对偏差(Rd)均小于15%,说明用该方法定量分析垃圾焚烧飞灰和烟气中PCDD/F毒性是可行的.     

PCDD/Fs emission, risk characterization, and reduction in China’s secondary copper production industry

Secondary copper production is one of the key polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) emission sources in China, but research and data on this issue are rare. In 2004, when the Stockholm Convention entered into force in China, PCDD/Fs emissions from secondary copper production contributed to 32.2% of the total release. In this paper, PCDD/Fs emission dynamics from secondary copper industry were discussed and cumulative risks were characterized. From 2004 to 2009, industrial policies played an indirect role in PCDD/Fs reduction, but its effects are still limited. The Yangtze River Delta, Pearl River Delta and central regions were among the top three of dioxin emissions from secondary copper production in China. Shanghai, Shandong, Zhejiang, and Jiangxi had comparatively higher accumulated risk and were recommended as the priority regions for promoting PCDD/Fs emission control in China. From 2009 to 2015, the PCDD/Fs emission dynamics in the secondary copper industry were presented through simulation. PCDD/Fs emission equations were established, resulting in the recommendation of control technology conversion rate at 30% for small scale smelters and 51%–57% for large and medium-sized enterprises in 2015. In conclusion, both indirect policy and direct control technology retrofitting should be integrated for more effective PCDD/Fs emission reduction in secondary copper industry.     

The Distribution and Impacts of Dioxins and Polychlorinated Biphenyls in the Taiwan Er-Jen River

The distribution and impacts of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/DFs) and polychlorinated biphenyls (PCBs) in the Taiwan Er-Jen River were investigated by monitoring fish distribution and measuring PCDD/DFs and PCBs levels in sediment and fish samples. Most of the fish collected are pollution-resistant species such as Oreochromis spp, Liza macrolepsis, Channa spp and Megalops cyprinoides. the most polluted river sections are in the upstream where large amount of waste effluents from households, livestock rearing and nearby dumping sites were discharged into the river, and the lower reaches of the river where metal recovery activities including open burning of waste electrical wire/scrap occurred. Sediment samples collected near the burning site show 2,3,7,8-TCDD toxicity equivalents (TEQ) ranging from 0.014 to 14.2 ng g^-1 by PCDD/DFs and from 0.015 to 1.03 ng g^-1 by coplanar PCBs (Co-PCBs). the fish samples show TEQ ranging from 0.029 to 0.615 ng g^-1 by PCDD/DFs and from 0.012 to 0.12 ng g^-1 by Co-PCBs. Possible PCDD/DFs sources are discharged PCBs, open burning of waste wire/scrap, and pentachlorophenol. the consumption of these fish will cause an average intake of 54 pg kg^-1 d^-1 TEQ. the prevention of direct discharge of livestock and the dumping of waste effuents into River Er-Jen as well as the control of metal recovery activities appears to be the first step toward the restoration of River Er-Jen.     

The Distribution and Impacts of Dioxins and Polychlorinated Biphenyls in the Taiwan Er-Jen River

Abstract

The distribution and impacts of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/DFs) and polychlorinated biphenyls (PCBs) in the Taiwan Er-Jen River were investigated by monitoring fish distribution and measuring PCDD/DFs and PCBs levels in sediment and fish samples. Most of the fish collected are pollution-resistant species such as Oreochromis spp, Liza macrolepsis, Channa spp and Megalops cyprinoides. the most polluted river sections are in the upstream where large amount of waste effluents from households, livestock rearing and nearby dumping sites were discharged into the river, and the lower reaches of the river where metal recovery activities including open burning of waste electrical wire/scrap occurred. Sediment samples collected near the burning site show 2,3,7,8-TCDD toxicity equivalents (TEQ) ranging from 0.014 to 14.2 ng g^?1 by PCDD/DFs and from 0.015 to 1.03 ng g^?1 by coplanar PCBs (Co-PCBs). the fish samples show TEQ ranging from 0.029 to 0.615 ng g^?1 by PCDD/DFs and from 0.012 to 0.12 ng g^?1 by Co-PCBs. Possible PCDD/DFs sources are discharged PCBs, open burning of waste wire/scrap, and pentachlorophenol. the consumption of these fish will cause an average intake of 54 pg kg^?1 d^?1 TEQ. the prevention of direct discharge of livestock and the dumping of waste effuents into River Er-Jen as well as the control of metal recovery activities appears to be the first step toward the restoration of River Er-Jen.     

北京市农业区不同使用类型土壤中二噁英类分析

2005年6—7月采集了北京市农业区不同使用类型土壤样品24个,分别为蔬菜地8个、粮地8个、果园地8个,采用高分辨气质联机对17种二噁英类进行了分析.结果表明:所有样品中二噁英浓度范围为,0.26—5.74(平均值为1.51)pgI-TEQ.g-1;蔬菜地浓度范围为,0.26—5.62(平均值1.75)pgI-TEQ.g-1;粮地浓度范围为,0.45—5.74(平均值2.02)pgI-TEQ.g-1;果园地浓度范围为,0.34—2.02(平均值0.73)pgI-TEQ.g-1;三种类型中粮食地浓度最高,其次为蔬菜地,果园地浓度最低.与国外农业区土壤中的二噁英浓度相比而言,北京市相对较低.所有样品中,样品8和16浓度异常高,但是8.3%(2:24)的高浓度样品数并不代表对人体有害.由于样品24处于垃圾焚烧炉旁边,也对此进行了详细的分析.样品中二噁英类物质形态分布出现了极大的离散性,这表明农田土壤中二噁英可能是多种因素综合作用的结果,例如:除草剂的使用、秸秆等固体废弃物的焚烧、汽车尾气排放等.     

Oral bioaccessibility of inorganic contaminants in waste dusts generated by laterite Ni ore smelting

The laterite Ni ore smelting operations in Niquelândia and Barro Alto (Goiás State, Brazil) have produced large amounts of fine-grained smelting wastes, which have been stockpiled on dumps and in settling ponds. We investigated granulated slag dusts (n = 5) and fly ash samples (n = 4) with a special focus on their leaching behaviour in deionised water and on the in vitro bioaccessibility in a simulated gastric fluid, to assess the potential exposure risk for humans. Bulk chemical analyses indicated that both wastes contained significant amounts of contaminants: up to 2.6 wt% Ni, 7580 mg/kg Cr, and 508 mg/kg Co. In only one fly ash sample, after 24 h of leaching in deionised water, the concentrations of leached Ni exceeded the limit for hazardous waste according to EU legislation, whereas the other dusts were classified as inert wastes. Bioaccessible fractions (BAF) of the major contaminants (Ni, Co, and Cr) were quite low for the slag dusts and accounted for less than 2 % of total concentrations. In contrast, BAF values were significantly higher for fly ash materials, which reached 13 % for Ni and 19 % for Co. Daily intakes via oral exposure, calculated for an adult (70 kg, dust ingestion rate of 50 mg/day), exceeded neither the tolerable daily intake (TDI) nor the background exposure limits for all of the studied contaminants. Only if a higher ingestion rate is assumed (e.g. 100 mg dust per day for workers in the smelter), the TDI limit for Ni recently defined by European Food Safety Authority (196 µg/day) was exceeded (324 µg/day) for one fly ash sample. Our data indicate that there is only a limited risk to human health related to the ingestion of dust materials generated by laterite Ni ore smelting operations if appropriate safety measures are adopted at the waste disposal sites and within the smelter facility.     

Site-specific bioaccumulation of polychlorinated dibenzo-<Emphasis Type="Italic">p</Emphasis>-dioxins and polychlorinated dibenzofurans (PCDD/PCDFs) in mothers and their infants living in vicinity of Bien Hoa airbase,Southern Vietnam

Bien Hoa airbase is located in Dong Nai Province (Southern Vietnam). Several sites within the airbase are highly contaminated by Agent Orange/Dioxin, and thus, they are also commonly named as an Agent Orange/Dioxin hotpot. In the present study, 36 maternal milk samples were collected from primiparas who have lived at least 5 years in four wards, Buu Long, Quang Vinh, Trung Dung and Tan Phong, which are closed to Bien Hoa airbase in order to investigate the level and distribution of Agent Orange/Dioxin exposure in different local communities. The mean concentrations of PCDD/PCDFs in four investigated wards range from 6.4 to 13.6 pgTEQ/g lipid. The highest mean TEQ of PCDD/PCDFs was observed in Buu Long ward (13.6 pgTEQ/g lipid), followed by Tan Phong ward (12.3 pgTEQ/g lipid), and the lowest value was observed in Trung Dung ward (6.4 pgTEQ/g lipid). The mean concentration of 2,3,7,8-TCDD in Buu Long (7.6 pg/g lipid) was approximately 2–6 times higher than those in Tan Phong (3.9 pg/g lipid), Quang Vinh (2.3 pg/g lipid), or Trung Dung (1.2 pg/g lipid). These results imply site-specific exposure to PCDD/PCDFs in different local communities living around Bien Hoa airbase. The mean values of daily intake of dioxin estimated for the breast fed infants living in Buu Long, Quang Vinh, Trung Dung and Tan Phong were about 80, 37.5, 31.7 and 58 pg TEQ/kg bw/day, respectively.     

典型电子垃圾拆解区二噁英污染特征、相分配及暴露风险

选取南方某典型电子垃圾拆解区不同作业区为研究对象,重点研究了拆解地大气中二噁英的污染特征、气相-颗粒相分配及呼吸暴露风险。通过对5个采样点（包括1个背景点）的研究发现,电子垃圾拆解作业区颗粒相ΣPCDD/Fs的质量浓度为：20.64-56.14 pg·m^-3,毒性当量为：I-TEQ 0.293-1.490 pg·m^-3;气相ΣPCDD/Fs的质量浓度为：3.861-19.29 pg·m^-3,毒性当量为：I-TEQ 0.384-2.150 pg·m^-3。背景点大气中二噁英浓度相对较低,颗粒相和气相样品中质量浓度值分别为：3.734 pg·m^-3和2.637 pg·m^-3,毒性当量仅为I-TEQ 0.176-0.267 pg·m^-3;要明显低于电子垃圾拆解区。基于污染物气相-颗粒相分配系数与蒸汽压的关系对二噁英的气-固分配行为研究显示,除了拆解混合作业区有较好的分配系数（-0.64）外,其它监测点位二噁英的气-固平衡状态较弱（-0.27--0.03）,更多的是以低分子量的单体化合物赋存于气相样品中。对拆解区二噁英呼吸暴露风险研究结果表明,儿童呼吸暴露风险要高于成年人;同时无论是儿童还是成年人,其二噁英的呼吸暴露量均要高于国内外城市报道的二噁英人体呼吸暴露量,说明本次监测的电子垃圾拆解区存在的潜在健康风险不容忽视。     

Distribution,seasonal variation and inhalation risks of polychlorinated dibenzo-<Emphasis Type="Italic">p</Emphasis>-dioxins and dibenzofurans,polychlorinated biphenyls and polybrominated diphenyl ethers in the atmosphere of Beijing,China

Spatial distribution, seasonal variation and potential inhalation risks of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) were investigated in the atmosphere of Beijing, using passive air samplers equipped with polyurethane foam disks. Concentrations of ΣPCDD/Fs, ΣPCBs and ΣPBDEs ranged from 8.4 to 179 fg WHO₂₀₀₅-TEQ/m³, 38.6–139 and 1.5–176 pg/m³, respectively. PCDFs showed higher air concentrations than those of PCDDs, indicating the influence of industrial activities and other combustion processes. The non-Aroclor congener, PCB-11, was detected in air (12.3–99.4 pg/m³) and dominated the PCB congener profiles (61.7–71.5% to ∑PCBs). The congener patterns of PBDEs showed signatures from both penta-BDE and octa-BDE products. Levels of PCDD/Fs, PCBs and PBDEs at the industrial and residential sites were higher than those at rural site, indicating human activities in urban area as potential sources. Higher air concentrations of PCDD/Fs, PCBs and PBDEs were observed in summer, which could be associated with atmospheric deposition process, re-volatilization from soil surface and volatilization from use of technical products, respectively. Results of inhalation exposure and cancer risk showed that atmospheric PCDD/Fs, dioxin-like PCBs and PBDEs did not cause high risks to the local residents of Beijing. This study provides further aid in evaluating emission sources, influencing factors and potential inhalation risks of the persistent organic pollutants to human health in mega-cities of China.     

Levels and patterns of polychlorinated biphenyls in residues from incineration of established source-classified MSW in China

Municipal solid waste (MSW) source-classified collection represents an advancement in resource cycling and secondary pollution control in China. Comparative experiments were performed to assess the levels and patterns of polychlorinated biphenyls in bottom ash, fly ash from boiler, and fly ash from bag filter from an MSW incineration plant with source-classified collection of MSW. Polychlorinated biphenyls were concentrated in the bag filter fly ash and in the bottom ash. The total amount of polychlorinated biphenyls was much lower than in fly ashes and bottom ash from traditional mixed waste incineration. Total concentration of coplanar polychlorinated biphenyls and toxic equivalent quantities were also reduced. Due to variations of feed waste, complete combustion, including continuously high incineration temperature, low CO concentrations and high air excess ratio were observed. Incineration temperature showed a negative correlation, while CO concentration showed a positive correlation with total and coplanar polychlorinated biphenyls, indicating that the latter can be reduced by controlling combustion conditions related to properties of feed waste.     

Teil 2: PCDD/F,Biphenyle und Organochlorpestizide in Frauenmilch

After the discovery of high dioxin levels (>100 000 ng TE BGA/kg) in copper slag (Kieselrot) from a specific chlorinating roasting process performed in Marsberg, human milk samples from mothers living in Marsberg were analyzed for polychlorinated dibenzo-p-dioxins (PCDD), dibenzofurans (PCDF) and other pollutants. PCDD/F levels in all samples were comparable with levels in human milk samples from other locations in the Federal Republic of Germany. An increase in congeners, especially of those predominating in ?Kieselrot“, could not be measured. Although several thousand tons of dioxin contaminated copper slag still lie on the slagheap, a higher burden in human milk from Marsberg could not be observed.     

Legacies and health risks of heavy metals,polybrominated diphenyl ethers,and polychlorinated dibenzo-dioxins/furans at e-waste recycling sites in South China

● Heavy metals and organic toxins may persist in legacy sites for a long time. ● Contaminants pose potential harms to the nearby community (HI > 1). ● PCDD/Fs had the risk of endocrine disruption and reproductive risk. ● Further intervention is needed to reduce pollution and related risks. Informal electronic-waste (e-waste) recycling sites pose substantial health risks to surrounding environments and populations, yet they are not properly regulated. In this study, the soil levels of copper, lead, cadmium, eight polybrominated diphenyl ethers (PBDEs), and 18 polychlorinated dibenzo-dioxins/furans (PCDD/Fs) were measured at two e-waste recycling sites in South China between 2014 and 2019. Both sites have been abandoned for natural restoration. Our results indicate that the mean Cd and PCDD/F levels at Site A in 2019 were higher than those recommended by current safety guidelines. Meanwhile, the highest exposure among children was 1.36 × 10⁻² mg/(kg·d) for Cu, followed by 5.05 × 10⁻³ mg/(kg·d) for Pb, 9.71 ng/(kg·d) for PBDEs, and 6.82 ng TEQ/(kg·d) for PCDD/Fs. Children were at elevated risk for health problem posed by Pb and Cu exposure at both sites (hazard quotient > 1) and by PCDD/Fs at Site A. Further risk assessment was conducted on the target organs and endpoints of heavy metals and PCDD/Fs. The hazard index (HI) for the target organ mixed-risk of heavy metals was high (HI = 1.27), as was that of PCDD/Fs (HI = 1.66), which can disrupt endocrine function and pose a risk of reproductive toxicity in children. Owing to incomplete cleaning, contaminants persist in soils over long periods and may harm nearby environments and communities. Our study demonstrates that heavy metal, PBDE, and PCDD/F contamination have not yet been remediated, and intervention is needed to reduce pollution and associated risks in areas affected by e-waste.