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141.
142.
地下水浅埋区某加油站特征污染物空间分布简 总被引:2,自引:0,他引:2
加油站渗漏污染地下水已经是一个世界性的问题。由于浅埋区加油站储罐与地下水密切接触,更加剧储罐的腐蚀。为揭示加油站渗漏的典型污染物石油烃(TPH)、苯系物(BTEX)、萘和甲基叔丁基醚(MTBE)在该水文地质条件下的迁移变化,在浅埋区某加油站开展了平、枯、丰水期的地下水监测工作。在水平分布上,TPH、BTEX、萘基本相似,均在加油岛附近形成高浓度区,而MTBE则更易随地下水流动而迁移,呈现出不同的污染晕。在垂直分布上,地下水的水位变动是污染物浓度分布的主要影响因素。 相似文献
143.
关伟 《辽宁城乡环境科技》2000,20(4):40-41
介绍了脂肪聚氧乙烯醚(0~15)羧酸盐的合成和性能。通过正交确定了较佳的合成工艺条件,并对其进行红外光谱的实验测试。 相似文献
144.
Detection of a Toxic Product Released by a Polyurethane-Containing Film Using a Composting Test Method Based on a Mineral Bed 总被引:1,自引:0,他引:1
Maurizio Tosin Francesco Degli-Innocenti Catia Bastioli 《Journal of Polymers and the Environment》1998,6(2):79-90
The degradation of a film containing a 4,4diphenyl methane diisocyanate (MDI) poly(€-caprolactone)-based polyurethane was followed in a test system based on a mineral solid bed designed to facilitate analysis of break-down products released under composting conditions. The use of a mineral solid bed can help extraction and analytical procedures which could be hindered by the heterogeneous nature of compost. The fermentation conditions are typical of the composting environment and generate a powerfully degradative environment. The film fully disintegrated within 30 days of treatment. Analysis on the mineral bed extracts showed that: (i) about 40% of the initial polyurethane was still present in the bed extracts; (ii) this residue was strongly degraded in the poly(€-caprolactone) part, while the urethane part was almost completely recovered (from 80 to 95%, according to the measurement method); (iii) 4,4 diamino diphenyl methane (MDA), a very dangerous product of MDI, was released during biodegradation. The results indicate that a mineral bed can be employed to study degradation and metabolites formation in solid phase fermentation and that the MDI-based polyurethanes are not susceptible of a full degradation during composting and maintain the potential of a slow release of MDA into the environment after soil application. 相似文献
145.
研究了185nm紫外光降解水中二苯甲酮和孔雀石绿和总有机碳(TOC)的规律.研究了浓度、体积、流速、pH等因素对二苯甲酮的降解效果的影响.通过改变污染物初始浓度、体积、流量、pH值以及添加无机离子来讨论185nm紫外光对孔雀石绿的降解效果,探讨了降解的最佳条件.降解达到了治理水中二苯甲酮和孔雀石绿污染的目的.用这种方法降解水中二苯甲酮和孔雀石绿,去除率能够达到99.9%以上,是一种非常有效的治理污染方法.实验同时验证了185nm UV降解水中的二苯甲酮和孔雀石绿符合准一级动力学规律. 相似文献
146.
Brominated flame retardants and polychlorinated biphenyls in fish from the river Scheldt, Belgium 总被引:1,自引:0,他引:1
Roosens L Dirtu AC Goemans G Belpaire C Gheorghe A Neels H Blust R Covaci A 《Environment international》2008,34(7):976-983
Levels of polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDs), and polychlorinated biphenyls (PCBs) were measured in several fish species originating from the river Scheldt (Belgium). Five sampling locations were chosen in a highly industrialized area along the river, while two ponds in the vicinity of the river served as reference sites. The present study is a follow-up of a survey performed in 2000 which reported extremely high levels of PBDEs and HBCDs in eel (Anguilla anguilla) collected from the same region (Oudenaarde, Flanders). The sum of tri- to hepta-BDE congeners (2270+/-2260 ng/g lipid weight (lw), range 660-11500 ng/g lw) and total HBCDs (4500+/-3000 ng/g lw, range 390-12100 ng/g lw) were one order of magnitude higher than levels usually reported from freshwater systems, indicating the presence of point sources. In most samples, levels of total HBCDs were higher than those of PBDEs, probably due to the high density of factories using HBCD as an additive brominated flame retardant (BFR). The high values of HBCDs were confirmed by both gas- and liquid-chromatography-mass spectrometry. Although BFR levels were between the highest ever reported in freshwater ecosystems, PCBs could be detected at even higher concentrations (16000+/-14300 ng/g lw, range 3900-66600 ng/g lw), being among the highest levels recorded in Belgium. The inter-sampling site variation of PBDEs, HBCDs and PCBs was comparable. All locations presented similar PBDE congener profiles, with BDE 47 being the dominant congener, followed by BDE 100, BDE 99 and BDE 49, probably originating from the former use of the penta-BDE technical mixture. In order to estimate the impact of these point sources on human exposure, we further focussed on eels which showed a considerable decrease in the PBDE and HBCD levels between 2000 and 2006. Due to the wide span in concentrations between the different sampling locations, a variable contribution to the total human exposure through local eel consumption was estimated. The calculated daily intake ranged from 3 ng to 330 ng PBDEs/day for normal eel consumers, but was as high as 9800 ng PBDEs/day for anglers, which may be considered at risk. 相似文献
147.
Yue Li Yan-Ping Duan Fan Huang Jing Yang Nan Xiang Xiang-Zhou Meng Ling Chen 《Waste management (New York, N.Y.)》2014,34(6):1059-1065
Very few data for polybrominated diphenyl ethers (PBDEs) were available in the electronic waste (e-waste) as one of the most PBDEs emission source. This study reported concentrations of PBDEs in e-waste including printer, rice cooker, computer monitor, TV, electric iron and water dispenser, as well as dust from e-waste, e-waste dismantling workshop and surface soil from inside and outside of an e-waste recycling plant in Shanghai, Eastern China. The results showed that PBDEs were detected in the majority of e-waste, and the concentrations of ΣPBDEs ranged from not detected to 175 g/kg, with a mean value of 10.8 g/kg. PBDEs were found in TVs made in China after 1990. The mean concentrations of ΣPBDEs in e-waste made in Korea, Japan, Singapore and China were 1.84 g/kg, 20.5 g/kg, 0.91 g/kg, 4.48 g/kg, respectively. The levels of ΣPBDEs in e-waste made in Japan far exceed the threshold limit of RoHS (1.00 g/kg). BDE-209 dominated in e-waste, accounting for over 93%. The compositional patterns of PBDEs congeners resembled the profile of Saytex 102E, indicating the source of deca-BDE. Among the samples of dust and surface soil from a typical e-waste recycling site, the highest concentrations of Σ18PBDEs and BDE-209 were found in dust in e-waste, ranging from 1960 to 340,710 ng/g and from 910 to 320,400 ng/g, which were 1–2 orders of magnitude higher than other samples. It suggested that PBDEs released from e-waste via dust, and then transferred to surrounding environment. 相似文献
148.
采用动态吸附法研究了5种活性炭纤维(ACF)对乙醇、乙醚及模拟混合废气中的乙醇和乙醚的吸附性能。实验结果表明:当ACF-1,ACF-2,ACF-3,ACF-4分别吸附乙醇和乙醚时,在室温、乙醇质量浓度12.0 mg/L、乙醚质量浓度13.0 mg/L的条件下,4种ACF对乙醇的穿透吸附量和饱和吸附量分别为60~70 mg/g和339~409 mg/g,对乙醚的穿透吸附量和饱和吸附量分别为50~65 mg/g和301~344 mg/g;在室温、模拟混合废气中乙醇和乙醚的质量浓度均为11.6 mg/L、吸附时间120 min的条件下,具有较大的比表面积和微孔体积的ACF-5对乙醇的吸附量为205 mg/g,对乙醚的吸附量为223 mg/g;在脱附真空度-0.95 Pa、脱附时间20 min的条件下,经17 次使用的ACF-5对模拟混合废气中乙醇和乙醚的穿透吸附量均为87 mg/g,穿透时间均为12 min。 相似文献
149.
Anna Christiansson Johan Eriksson Daniel Teclechiel Åke Bergman 《Environmental science and pollution research international》2009,16(3):312-321
Background, aim, and scope Decabromodiphenyl ether (DecaBDE) is used as an additive flame retardant in polymers. It has become a ubiquitous environmental
contaminant, particularly abundant in abiotic media, such as sediments, air, and dust, and also present in wildlife and in
humans. The main DecaBDE constituent, perbrominated diphenyl ether (BDE-209), is susceptible to transformations as observed
in experimental work. This work is aimed at identifying and assessing the relative amounts of products formed after UV irradiation
of BDE-209.
Materials and methods BDE-209, dissolved in tetrahydrofuran (THF), methanol, or combinations of methanol/water, was exposed to UV light for 100
or 200 min. Samples were analyzed by gas chromatography/mass spectrometry (electron ionization) for polybrominated diphenyl
ethers (PBDEs), dibenzofurans (PBDFs), methoxylated PBDEs, and phenolic PBDE products.
Results The products formed were hexaBDEs to nonaBDEs, monoBDFs to pentaBDFs, and methoxylated tetraBDFs to pentaBDFs. The products
found in the fraction containing halogenated phenols were assigned to be pentabromophenol, dihydroxytetrabromobenzene, dihydroxydibromodibenzofuran,
dihydroxytribromodibenzofuran, and dihydroxytetrabromodibenzofuran. The PBDEs accounted for approximately 90% of the total
amount of substances in each sample and the PBDFs for about 10%.
Discussion BDE-209 is a source of PBDEs primarily present in OctaBDEs but also to some extent in PentaBDEs, both being commercial products
now banned within the EU and in several states within the USA. It is notable that OH-PBDFs have not been identified or indicated
in any of the photolysis studies performed to date. Formation of OH-PBDFs, however, may occur as pure radical reactions in
the atmosphere.
Conclusions Photolysis of decaBDE yields a wide span of products, from nonaBDEs to hydroxylated bromobenzenes. It is evident that irradiation
of decaBDE in water and methanol yields OH-PBDFs and MeO-PBDFs, respectively. BDE-202 (2,2′,3,3′,5,5′,6,6′-octabromodiphenyl
ether) is identified as a marker of BDE-209 photolysis.
Recommendations and perspectives BDE-209, the main constituent of DecaBDE, is primarily forming debrominated diphenyl ethers with higher persistence which
are more bioaccumulative than the starting material when subjected to UV light. Hence, DecaBDE should be considered as a source
of these PBDE congeners in the environment.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
150.
Foster WG Gregorovich S Morrison KM Atkinson SA Kubwabo C Stewart B Teo K 《Chemosphere》2011,84(10):1301-1309
Polybrominated diphenyl ethers (PBDEs), widely used as flame retardants in commercial products, have become ubiquitous environmental contaminants. Although adult human exposure to PBDEs is well documented, developmental exposure is less well characterized. The objectives of this study were to measure maternal and fetal exposure to nine PBDE congeners and to investigate potential associations with birth weight. PBDE congeners were quantified in maternal serum at 24-28 weeks of pregnancy, delivery, and umbilical cord serum (UCS) by gas chromatography-mass spectrometry (GC/MS/MS). Complete blood sample sets were obtained from 97 pregnant women (mean age 33.1 ± 0.5 years). PBDE-28, -47 and -99 were quantified in all samples tested and PBDE-47 was the most abundant congener measured in both maternal (mid-pregnancy and delivery samples geometric mean = 26.9 and 26.9, respectively) and UCS (GM = 56.0 ng g−1 lipid). The UCS concentration for all congeners with the exception of PBDE-153 was higher vs. maternal delivery samples (p < 0.001). Only the UCS concentration of PBDE-17 and -99 were significantly associated (β = −49.860, p = 0.032, and β = −3.645, p = 0.05) with birth weight. However, after adjustment for potential confounders only the association between PBDE-99 and birth weight remained significant (β = −3.951 and p = 0.016). We conclude that: the fetus is exposed to PBDEs from at least the second trimester of pregnancy onward; PBDE congeners are higher in UCS compared to maternal serum samples collected at delivery; and that developmental PBDE exposure is potentially associated with lower birth weight. 相似文献