利用生态混凝土控制城市坡面暴雨径流污染试验研究

利用生态混凝土作为护坡材料,研究暴雨条件下生态混凝土控制山坡降雨径流污染的机理,以期对生态混凝土在城市护坡和护岸中的应用提供理论依据.研究结果表明,生态混凝土改变了雨水在坡面上的水文过程,阻延径流作用十分明显,有效地降低了污染物的负荷输出.生态混凝土试验小区(T2)与裸地(CK)和改良土壤小区(T1)相比,径流量分别减少了48%和24%,TN年度污染负荷(UPLRs)分别减少了53%和45%,溶解态氮(DN)减少了26%和28%,TP减少了57%和30%,溶解态磷(DP)降低了80%和33%,COD降低了62%和40%,TSS降低了56%和43%,产流时间和流量峰均明显滞后.另外,同植被覆盖良好的小区(T3)相比,生态混凝土对各种污染指标的控制效果没有明显差异,但其抗冲刷能力较强,更能适应城市护坡和护岸的需要.     

西安市城市主干道路面径流初期冲刷效应

以西安市城市主干道南二环太白路高架桥为路面径流采样区域,采用人工等时间间隔采样方法,在桥梁排水立管对2010年9—11月的3场径流事件进行全程采样,测试径流过程SS、COD、溶解性COD、NH3-N、Pb、溶解性Pb、Zn和溶解性Zn的浓度变化,研究路面径流的初期冲刷效应及其影响因素。结果表明,西安市城市主干道路面径流污染严重,降雨数小时后的末期径流仍具有较高的污染水平;径流过程污染物浓度变化规律与其赋存形态有关,SS、COD、Pb等以颗粒态为主的污染物的浓度随雨强变化剧烈波动,NH3-N、溶解态COD、溶解态Zn等以溶解态为主的污染物浓度变化受雨强影响较小,随径流过程呈逐渐减小趋势;路面径流初期冲刷现象并非普遍存在,与污染物的赋存状态和场次降雨特征密切相关,溶解态污染物易于出现初期冲刷现象,颗粒态污染物是否出现初期冲刷与场次降雨特征有关;测试的3场径流事件初期30%的径流携带的SS、COD、溶解性COD、NH3-N、Pb、Zn和溶解性Zn的负荷占场次径流总负荷的比例分别为21.8%～50.0%、25.5%～49.3%、36.3%～52.6%、52.6%～66.7%、26.8%～45.0%、27.2%～63.4%和36.2%～62.6%,表明仅对初期径流进行治理无法实现对西安市路面径流污染的有效控制。     

城市典型屋面径流的排污特征

对城市中典型的2种材料(油毡和水泥)屋面降雨径流中颗粒物(SS)、氮(N)和磷(P)污染物排放特征进行了研究。结果表明,屋面径流中颗粒物主要是以10~100μm粒径范围的颗粒物为主(约占75%),氮主要是以溶解态形式排放(80%~95%),且主要形式是以硝态氮和氨态氮为主,水泥屋面增加了径流中硝态氮的比例,而沥青屋面增加了氨态氮和溶解态有机氮的比例。而磷主要是以颗粒物形态排放(约占40%~70%,平均57.5%),且主要结合10~50μm粒径范围的颗粒物。去除10~50μm粒径颗粒物可以降低屋面径流中50%颗粒物和47.9%磷的排放,而氮却需采用不同处理方法。同时,EC和TSS与TN和TP相关关系表明,EC和TSS可分别作为屋面降雨径流溶解态氮和颗粒态磷污染程度检测和评价指示指标。研究结果为有效地去除降雨径流中污染物、降低城市面源污染对水环境的影响,提供了一定的科学依据。     

上海市城区径流污染及控制对策

随着城市点源污染控制程度的提高,雨水径流引起的面源污染日益突出.非渗透性地表径流污染成为城市水体污染的主要来源.对上海市城区非渗透性地表径流进行了为期3年的采样调查,监测了COD、BOD5、SS、NH3-N、TP和TN等污染物指标,并估算了单位面积径流年污染负荷.结合上海市实际情况,提出了城区径流污染控制的综合策略.     

基于旱作农田面源污染控制的生态沟渠构建及其拦截效果研究

针对南方平原河网地区旱作农田径流排水特征,构建了一种混凝土多孔板结构的生态沟渠,有效过水断面为0.8m~2,稳定期沟壁和沟底净化植物生物量分别为0.54、0.36kg/m,并通过引入三维植被网护坡技术,在发挥生态拦截功能的同时,大大提高了沟渠抗坡面侵蚀强度。试验表明,径流排水的水力停留时间(HRT)达48h时,生态沟渠对悬浮物(SS)、总氮(TN)和总磷(TP)拦截率分别为50.5%、53.6%、56.1%。生态沟渠对硝态氮的拦截规律与TN一致,但对可溶性磷(DP)的拦截效果与传统水旱通用混凝土排水渠无明显差别,说明生态沟渠对TP的拦截主要表现在对颗粒吸附态磷的拦截。     

城市区域不同屋顶降雨径流水质特征

城市屋顶降雨径流是城市面源污染的主要组成部分之一。为了解城市不同屋顶降雨径流的水质特性,以重庆地区5种屋顶为例进行了20场降雨径流的水质监测。研究结果表明,不透水屋顶降雨径流污染物浓度均随降雨历时的延长而降低,混凝土屋顶降雨径流的COD、TP、TN、NH3-N平均浓度分别是瓦屋顶的1.6、1.7、1.4和1.5倍,且不透水屋顶降雨径流总氮的70%~80%为无机氮,总磷的20%~32%为磷酸盐;浅层屋顶降雨径流COD、TN、TP、NH3-N和NO-3-N浓度分别是深层绿色屋顶的0.25~0.26、0.3~0.5、0.07~0.09、0.3~0.6、0.05~0.06倍,且绿色屋顶降雨径流总氮的60%~80%为硝态氮。前期干旱天数和混凝土屋顶径流中的TN、接骨草屋顶径流中的氨氮浓度呈显著正相关关系,混凝土屋顶径流TP浓度与降雨强度显著正相关,降雨持续时间和瓦屋顶径流TSS平均浓度显著正相关。研究结果为城市建筑屋顶降雨径流的科学管理提供了参考。     

降雨促渗对地表径流污染物负荷影响模拟试验研究

建立模拟降雨装置,研究降雨条件下功能性材料与聚合物对降水土壤渗透性与地表径流污染负荷的影响.研究证实,沸石与PAM不仅能够促进降雨土壤水的入渗、延缓并减少地表径流,而且使土壤渗液和地表径流水质TSS、TN、TP、COD污染物负荷降低.以3 kg/hm2 PAM、3 kg PAM与7.5 t/hm2沸石、6 kg/hm2 PAM 3种方式处理,径流COD负荷为对照的39.12%～69.76%、26.14%～46.63%和20.60%～28.09%;TN、TP与TSS负荷较对照分别减少44.36%～96.47%、66.63%～98.99%、93.71%～99.62%和50.46%～98.40%、83.30%～99.31%、94.91%～99.72%和31.06%～77.23%、46.82%～86.22%、83.54%～95.33%.聚合物与功能性材料改良土壤是一种削减地表降雨径流非点源污染的有效手段.     

昆明主城区城市地表径流污染特征分析

昆明市位于滇池上游,城市地表径流污染负荷对滇池水质具有直接影响。通过对昆明主城区内不同功能区12个监测点7次降雨径流过程水样的采集与分析,研究了昆明主城区城市地表径流污染特征。结果表明,昆明主城区城市地表径流中TSS、COD、TN和TP的多场降雨平均浓度分别为182.8、138.2、2.37和0.43 mg/L。不同功能区的地表径流水质存在显著差异(p<0.05);各功能区径流污染负荷顺序为:公路区>商业区>住宅区>文教区;不同功能区单场降雨径流水质动态变化规律是:污染物浓度在降雨径流初期相对较高,中后期浓度快速下降,并逐渐趋于稳定;地表利用功能、降雨特征和交通流量是影响城市地表径流水质的主要因素;城市地表径流中COD、TN、TP与TSS之间有较好的相关性,说明大部分的污染物质是以颗粒吸附态存在。     

北京市城区雨水径流污染控制与节能减排

节能减排是目前中国建设和谐社会、实施可持续发展的重大战略方针.随着城市生活污水处理率和工业废水达标率的不断提高以及清洁生产技术与管理体系的大力推行,城市雨水径流污染在水环境污染排放总量中所占比例越来越大.以北京市为例,2006年城八区生活污水处理率已达到90.0%.雨水径流COD排放量占废水COD排放总量的33.39%,足见城市径流污染已成为节能减排的重要方面,亟需全社会的广泛关注.控制城市雨水径流污染应从加强雨水径流污染的监管力度下手,建立以市场激励为主、政府管制为辅的雨水政策框架.     

人工湿地对城市住宅区降雨径流中铅的去除效果研究

根据重庆市棕榈泉住宅区雨水径流处理人工湿地的进水特点和运行特点,考察了该人工湿地恒定负荷下对铅的长期去除效果和单场降雨冲击负荷下铅的去除效果。结果表明,住宅区径流中铅浓度随季节性降雨特征变化明显,主要以非溶解态存在。在平均HRT为56 h的日常进水负荷下,人工湿地对铅长期表现出明显而稳定的去除作用,平均去除率达到84.9%,去除负荷达到10.5 mg/(m2.d),出水浓度和去除率受季节变化影响不明显。铅浓度在人工湿地内沿程下降,湿地系统前端潜流床内的去除作用最为明显。在冲击负荷分别为7.3和8.7倍日常负荷、持续时间分别为1.5和2.5 h的两场降雨中,人工湿地铅平均去除率分别为73.22%和38.12%。人工湿地对暴雨高冲击负荷具有明显的缓冲作用,对铅的去除效果受单场降雨进水流量曲线、进水水质曲线以及雨前储存容积大小的影响明显。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

The variation of street air levels of PAH and other mutagenic PAC in relation to regulations of traffic emissions and the impact of atmospheric processes

The occurrence of particle associated PAH and other mutagenic PAC was determined in 1996 in the street air of Copenhagen. In addition, particle extracts were tested for mutagenicity. The measurements were compared with previous measurements in 1992/1993. The levels had decreased in this period. The decrease was caused by an implementation of light diesel fuels for buses and the exchange of older petrol-driven passenger cars with catalystequipped new ones. About 65% of the reduction was caused by the application of the light diesel fuels. Under special conditions, chemical processes in the atmosphere produced many more mutagens than the direct emissions. The concentrations of S-PAC and N-PAC were 10 times lower than those of PAH, while the levels of oxy-PAH were in the same order of magnitude as those of PAH. Benzanthrone, an oxy-PAH, is proposed to be formed in the atmosphere in addition to direct emissions. Benzo(a)pyrene, often applied as an air quality criteria indicator, was photochemically degraded in the atmosphere. A strong increase in the mutagenic activities was observed to coincide with a depletion of benzo(a)pyrene.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

Teratological effects of pesticides in vertebrates: a review

Abstract

In the last decades, the use and misuse of pesticides in the agriculture have increased, having a severe impact on ecosystems and their fauna. Although the various effects of pesticides on biodiversity have been already documented in several studies, to our knowledge no consistent overview of the impact of pesticides in vertebrates, both terrestrial and aquatic, is available. In this review, we try to present a concise compilation of the teratogenic effects of pesticides on the different classes of vertebrates – mammals, birds, reptiles, amphibians and fish.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.