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1.
硝酸盐对反硝化除磷过程的影响分析 总被引:4,自引:1,他引:3
在厌氧/缺氧间歇反应器内考察了硝酸盐进水浓度及进水方式对反硝化除磷过程的影响。结果表明:在缺氧阶段,反硝化除磷菌(DPBs)可将硝酸盐转化为亚硝酸盐,当硝酸盐浓度较低时,DPBs以亚硝酸盐为电子受体吸磷。进水COD浓度为220 mg/L,正磷浓度为6.8 mg/L,硝酸盐初始浓度为26 mg/L时,系统达到最佳脱氮除磷效果,期间亚硝酸盐浓度积累至10.71 mg/L。采用连续流投加硝酸盐的方式更利于氮磷的高效去除。 相似文献
2.
研究了低温条件下,沸石和火山岩为载体,锯末为碳源的生物反应器对地下水中硝酸盐氮的去除效果。结果表明,在(14±1)℃,水力停留时间18 h,进水硝酸盐氮浓度为27 mg/L的条件下,以锯末为碳源能有效去除地下水中的硝酸盐,沸石为载体时对硝酸盐氮的平均去除率为98%;火山岩为载体时对硝酸盐氮的平均去除率为95%。实验过程中出现铵盐和亚硝酸盐的积累,出水中氨氮浓度为1~2.55 mg/L,亚硝酸氮浓度为0~0.98 mg/L。出水pH均介于7~8,满足饮用水标准中pH的要求(6.5~8.5)。 相似文献
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4.
针对受硝酸盐污染的水源水,以琼脂为反硝化细菌的碳源和微生物载体,通过生物反硝化作用脱除水源水中的硝酸盐,并利用曝气生物滤池(BAF)去除琼脂反应器出水中残留的少量CODMn和NO2--N等污染物。实验结果表明,水源水自然接种的条件下,可以顺利启动琼脂反应器;在温度为25℃左右,琼脂反应器在进水NO3--N约25 mg/L、水力停留时间1.5 h时,能获得70%的硝酸盐氮去除率;曝气生物滤池在水力停留时间0.5 h、气水比2.8时,可控制最终出水的CODMn和NO2--N分别在5.0 mg/L和0.10 mg/L以下;琼脂反应器的脱氮效果与温度、进水NO3--N浓度及水力停留时间等有关。研究指出,琼脂反应器与曝气生物滤池构成的组合系统能较好地脱除水源水中的硝酸盐并且能控制最终出水水质,不会导致二次污染,从而获得合格的饮用水源水。 相似文献
5.
以可生物降解聚合为碳源的固相反硝化可以避免水产养殖用水硝酸盐处理过程中碳源反复添加、碳源不足或过量等问题。水力停留时间(hydraulic retention time, HRT)是生物反应器运行管理的主要参数之一, 用固定膜反应器固相反硝化的方法研究了HRT对以聚己内酯(polycaprolactone,PCL)为碳源的反应器去除循环水养殖系统硝酸氮(浓度为170~197 mg·L-1)的效率的影响。 研究结果表明不同水力停留时间对硝酸盐去除效率差异显著。在HRT 为6 h和8 h时,硝酸盐速率分别为(0.55±0.32) g·(L·d)-1和(1.05±0.33) g·(L·d)-1,且出水亚硝氮浓度和氨氮浓度均明显低于进水浓度;在HRT为4 h和2 h时,进出水硝酸盐浓度差异不明显。电子扫描显微镜观察显示PCL表面生物膜主要为杆状菌,应用傅里叶红外扫描观察发现使用前后PCL的化学结构没有发生明显改变。应用高通量方法测定的微生物群落结构表明,62%的细菌为Proteobacteria(62%),在鉴定出的细菌中,食酸菌属(Acidovorax), 固氮螺菌属(Azospira),丛毛单胞菌属(Comamonas), 代尔夫特菌属(Diaphorobacter), 懒小杆属(Ignavibacterium), 弗拉特氏菌属(Frateuria)可以同时降解PCL和进行反硝化。 相似文献
6.
考察了水力停留时间(HRT)对阴离子交换膜生物反应器去除硝酸盐的影响。实验结果表明,当进水NO3-浓度在113.96~116.01 mg/L范围内,HRT从11.12 h降低到4.82 h,硝酸盐去除率降低,但出水中NO3--N浓度符合我国饮用水水质标准中10 mg/L的要求(NO3-浓度≤44.29 mg/L)。厌氧生物反应器具有良好的反硝化性能,出水NO3-浓度低于20 mg/L。硝酸盐膜通量随着HRT的增加而增加,出水pH值稳定在7左右。 相似文献
7.
以红薯浸泡液为碳源的生物反硝化 总被引:3,自引:1,他引:2
为选择低碳氮比污水生物脱氮中合适的碳源,以搅拌罐浸泡淀粉类物质释放碳源,在确定利用红薯浸泡液为碳源后,以浸没式生物滤池为反应器进行生物反硝化实验。实验结果表明:20 g红薯置于2 L自来水中,采用250 r/m in的搅拌速度,搅拌频率为每搅拌3 h停1 h,2 d后得到的浸泡液COD浓度平均为5 921 mg/L,最高可超过7 000 mg/L;将此红薯浸泡液和污水以1∶50的流量比例,采用分别投加的方式进入反应器,污水中总氮、硝酸盐氮、亚硝酸盐氮及氨氮的平均去除率分别为88.6%、91.6%、88.2%和54.8%,出水COD平均在30 mg/L以下;在红薯浸泡液COD浓度为5 700 mg/L左右时,进水中亚硝酸盐氮浓度与硝酸盐氮浓度比为3∶2时总氮去除率为95.3%,当该比例为2∶3时总氮去除率为88.2%。研究表明,红薯浸泡液是一种经济合适的碳源,采用红薯浸泡液作为低碳氮比污水生物处理中反硝化的碳源是可行的。 相似文献
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9.
采用厌氧 缺氧SBR反应器对以硝酸盐作为电子受体的反硝化除磷过程进行了研究。结果表明 ,反硝化聚磷菌完全可以在厌氧 缺氧交替运行条件下得到富集。稳定运行的厌氧 缺氧SBR反应器的反硝化除磷效率 >90 % ,出水磷浓度 <1mg L。进水COD浓度对反硝化除磷的效率影响很大 ,在COD浓度 <180mg L时 ,进水COD浓度越高 ,除磷效率也就越高。较高浓度的进水COD浓度将导致有剩余的COD进入缺氧段 ,对反硝化吸磷构成不利影响。污泥龄为 16d时 ,厌氧 缺氧SBR反应器取得稳定和理想的反硝化除磷效果。污泥龄减少到 8d ,由于反硝化聚磷菌的流失导致反硝化除磷效率的下降。当污泥龄恢复到 16d时 ,经过一段时间的运行 ,反硝化聚磷菌重新得到富集 ,除磷效率恢复到 90 %以上。 相似文献
10.
玉米秸秆碳源释放特征及反硝化效果 总被引:4,自引:0,他引:4
通过静态和动态实验研究了玉米秸秆的碳源释放规律,并考察其浸出液作为反硝化碳源对高、中、低硝酸盐氮的去除效果。实验结果表明,玉米秸秆可有效地释放碳源物质,静态实验中,固液比为1:30时单位质量碳源释放的COD最多达254 mg/g,释放速率最快为13.37 mg/(g·d);动态实验中,秸秆长度为3 cm、水力停留时间(HRT)为48 h时,单位质量碳源释放的COD最多达826.26 mg/g,COD的速率最快为26.65 mg/(g·d)。反硝化过程中pH变化不明显,在7.0~8.0范围之间浮动。以玉米秸秆浸出液为反硝化碳源对中、低浓度的硝酸盐氮具有较好的去除效果,去除率保持在80%以上,甚至高达94%,但对高浓度的硝酸盐氮去除率仅在60%~80%之间。研究表明,玉米秸秆有较强的持续供碳能力,是一种经济合适的碳源材料,采用玉米秸秆浸出液作为去除地下水中硝酸盐氮的生物反硝化碳源是可行的。 相似文献
11.
Jaana Koistinen Sirpa Herve Raija Paukku Mirja Lahtiperä Jaakko Paasivirta 《Chemosphere》1997,34(12):2553-2569
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. 相似文献
12.
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. 相似文献
13.
G T Brooks 《Journal of environmental science and health. Part. B》2013,48(5):619-621
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. 相似文献
14.
Organochlorine compounds in a three-step terrestrial food chain 总被引:1,自引:0,他引:1
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. 相似文献
15.
Ralph A. Chapman Carol Harris 《Journal of environmental science and health. Part. B》2013,48(4-5):397-407
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. 相似文献
16.
Torben Nielsen Anders Feilberg Mona-Lise Binderup 《Environmental science and pollution research international》1999,6(3):133-137
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. 相似文献
17.
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. 相似文献
18.
Andreia Garcês Isabel Pires Paula Rodrigues 《Journal of environmental science and health. Part. B》2020,55(1):75-89
AbstractIn 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. 相似文献
19.
P.R. Fresquez J.D. Huchton M.A. Mullen L. Naranjo Jr. 《Journal of environmental science and health. Part. B》2013,48(5):611-622
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, 240Pu, 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. 相似文献
20.
Jennifer C. Anhalt Thomas B. Moorman William C. Koskinen 《Journal of environmental science and health. Part. B》2013,48(3):207-213
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. 相似文献