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1.
ABR-好氧颗粒污泥处理黄连素废水的启动研究   总被引:1,自引:0,他引:1  
实验研究了ABR-好氧颗粒污泥组合工艺处理黄连素制药废水的启动运行,通过分析发现,ABR装置在HRT为4 d,黄连素浓度为50 mg/L的运行方式下成功启动,反应器运行稳定后每个格室MLSS平均值分别为25 840、21 560、27 500和11 200 mg/L。以ABR出水为营养物,成功培养出粒径在2~10 mm,沉降速率为104~137 m/h,沉降性能优良的好氧颗粒污泥。该组合工艺在启动实验的末期,进水COD浓度为3 000~4 000 mg/L左右,出水COD浓度到达168.4~271mg/L,系统总的去除率保持在90%~95%之间,表明ABR-好氧颗粒污泥组合工艺能够有效地处理黄连素制药废水。  相似文献   

2.
常温下IC反应器启动过程中的颗粒污泥性能研究   总被引:6,自引:1,他引:5  
在常温下用自配葡萄糖废水启动IC反应器,研究了厌氧颗粒污泥的形成过程和特性。IC反应器进水浓度为3 000 mg COD/L,水温为14.5~26℃,25 d内形成了颗粒污泥。结果表明,随着运行时间和容积负荷的增加,颗粒污泥粒径逐渐增大。反应器启动完成后,反应器中2 mm的颗粒污泥增加到6.6%,0.3 mm的颗粒从57.7%减少到39.4%;VSS浓度从24.7 g/L上升到48.2 g/L;VSS/SS从34.4%增加到72.8%。颗粒污泥的沉降速度与颗粒粒径成正比,0.3~3 mm的颗粒污泥的沉降速度介于34.05~109.75 m/h之间,具有良好的沉降性能。初始接种污泥几乎没有产甲烷活性,与第30 d的初期颗粒污泥相比,成熟的颗粒污泥的产甲烷活性提高了46.7%。  相似文献   

3.
以絮状活性污泥为接种污泥,采用人工配制的模拟生活污水,分别在气提式序批反应器(SBAR)和序批式活性污泥反应器(SBR)中成功地培养出了成熟的好氧颗粒污泥.SBAR和SBR中的好氧颗粒污泥都具有稳定的基本形态结构,其微生物主要由杆菌和球菌组成,对COD的去除率可达到93%左右.对NH+4-N的去除率可达到98%以上.SBAR中好氧颗粒污泥的粒径主要分布、污泥体积指数(SVI)、比耗氧速率(SOUR)、TN去除率和TP去除率分别为0.45~2.00 mm、19.97 mL/g、47.68 g/(kg·h)、82%和65%;而SBR中好氧颗粒污泥的粒径主要分布、SVI、SOUR、TN去除率和TP去除率分别为0.18~1.00 mm、29.12 mL/g、43.21 g/(kg·h)、58%和50%.相对而言,SBAR更有利于好氧颗粒污泥的培养和运行.  相似文献   

4.
常温下向ABR反应器中加入惰性载体促进颗粒污泥形成   总被引:1,自引:1,他引:0  
常温条件下(21~25℃),用实验室规模的2个厌氧折流板反应器进行颗粒污泥培养实验,向其中一个反应器(称为B反应器)接种厌氧污泥的同时加入惰性载体,另一个反应器(称为A反应器)作为对照只接种厌氧污泥,考察了惰性载体对ABR反应器中颗粒污泥的形成和反应器运行效果的影响.结果表明,惰性载体的加入促进了反应器中颗粒污泥的形成,提高了反应器的处理效果.运行162 d后,B反应器每个隔室均出现大量颗粒污泥,4个隔室中粒径>0.5 mm的颗粒达到57.6%~72.7%;A反应器仅第1隔室中形成了大量颗粒污泥,其他3个隔室中粒径>0.5 mm的颗粒仅占11.3%~34.7%.COD去除率稳定保持在85%以上所需时间,B反应器比A反应器少用了51 d.  相似文献   

5.
聚丙烯酰胺废水的好氧颗粒污泥降解研究   总被引:1,自引:0,他引:1  
在序批式活性污泥反应器(SBR)内通过逐步提高进水中聚丙烯酰胺(PAM)的浓度实现了好氧颗粒污泥的驯化.经过43 d稳定运行,成功培养出性状良好且对PAM具有较高降解活性的PAM好氧颗粒污泥,其PAM平均降解速率达2.230 mg/(L·h).系统内PAM好氧颗粒污泥的混合液悬浮固体(MLSS)为9.85 g/L,污泥体积指数(SVI)为39.21 mL/g,湿污泥密度为1.034 g/cm3,平均粒径为1.85 mm,单个颗粒污泥的沉降速率为8.2~12.8 mm/s.  相似文献   

6.
以城市污水为处理对象,以絮状污泥为接种污泥,在连续流气提式好氧颗粒污泥流化床(CAFB)反应器中成功培养得到好氧颗粒污泥.探讨了CAFB中颗粒污泥的形成过程、生物多样性、有机物的去除行为及氮转化特性.研究结果表明,CAFB运行第7天颗粒污泥占主要优势,系统中依次出现原、后生动物,表明颗粒污泥趋于成熟.CAFB反应器中培养的好氧颗粒污泥具有良好的COD及NH4+-N去除能力.稳定运行阶段,当进水的COD容积负荷在1.5 ~3.5 kg COD/(m3·d)的范围时,COD的去除负荷稳定在1.0~2.0 kg COD/(m3·d).控制水力停留时间为(4 ±0.25)h、溶解氧质量浓度为(5 ±0.5) mg/L,可达到最高的硝化效率,但此控制条件下反硝化作用不明显.分析认为,作为完全混合式反应器的CAFB,需要较严格的控制溶解氧才能实现同步硝化反硝化作用.  相似文献   

7.
针对好氧颗粒污泥运行过程中稳定性较差的问题,在3个C/N比条件下,通过气升式内循环反应器对好氧颗粒污泥进行培养,分析了不同时期好氧颗粒污泥的沉降性能、粒径变化、进出水水质中有机物、胞外聚合物组分及含量变化,探讨了C/N比对好氧颗粒污泥稳定性的影响。结果表明,在C/N比分别为10、15和25的条件下,均能培养出好氧颗粒污泥,C/N比为15时,好氧颗粒污泥稳定性最优,此时好氧颗粒26 d内成NH_4~+-N和TP的去除率可达93%、75%和91%,松散型EPS和紧密型EPS的含量最高分别为44.97 mg·g~(-1)和54.20 mg·g~(-1)。在采用不同C/N比对好氧颗粒污泥的培养过程中,C/N比对好氧颗粒污泥稳定性有较大影响,其中松散型EPS与好氧颗粒污泥的稳定性呈正相关关系。  相似文献   

8.
在UASB反应器中接种好氧污泥培养厌氧颗粒污泥进行启动,研究不同浓度老龄(13年)垃圾渗滤液对处理效果的影响情况。通过保持进水COD浓度不变、逐步缩短HRT从而提高容积负荷到20 g COD/(L.d)的方法,可以培育出直径为1~3 mm颗粒污泥,最终产气量稳定在60~70 L/d,甲烷含量在50%~70%之间,COD去除率保持在90%左右,污泥层最底部MLSS为50 g/L。逐步提高进水中渗滤液的含量考察其对处理效果的影响,当进水为100%渗滤液时日产气量为500 mL/d、COD去除率仅为10%,表明渗滤液中多为难降解性有机物质。  相似文献   

9.
采用膜生物反应器进行含酚废水的处理,探讨投加好氧颗粒污泥对反应器中污泥性能的影响。结果表明,在膜生物反应器中投加好氧颗粒污泥能有效改善污泥性能,提高处理效果。从采用絮状污泥到逐渐增加好氧颗粒污泥投加量为100%的过程中,反应器中污泥浓度明显提高,MLSS由5 582 mg/L增加到8 168 mg/L;沉降性能得到改善,SVI由135.85 mL/g下降到29.36 mL/g;疏水性增强,Zeta电位由-20.302 mV升高到-4.325 mV;对含酚废水中COD、NH3-N的降解能力明显提高,COD、NH3-N、NO3-N去除率分别由87.3%、83.2%、55.3%增加到99.2%、94.9%、66.3%。改善了膜污染现象,膜通量衰减率由63.3%降低到42.8%。用二元多项式三维回归分析,得到污染物去除率关于好氧颗粒污泥投加量和反应器运行时间的二元方程,对指导好氧颗粒污泥膜生物反应器的连续运行具有重要意义。  相似文献   

10.
在UASB反应器中接种好氧污泥培养厌氧颗粒污泥进行启动,研究不同HRT对老龄(13年)垃圾渗滤液对处理效果的影响情况。通过保持进水COD浓度不变、逐步缩短HRT从而提高容积负荷到40 g COD/(L.d)的方法,可以培育出直径为1~3 mm颗粒污泥,最终产气量稳定在100 L/d,甲烷含量在60%~70%之间,COD去除率保持在90%左右,污泥层最底部MLSS为81 g/L。逐步提高HRT依次为6、12、24、48和72 h考察其对处理效果的影响,当HRT为24 h时处理效果最好,COD去除率最高达到35%左右。  相似文献   

11.
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   

12.
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   

13.
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   

14.
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.  相似文献   

15.
Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for 3H, 90Sr, 137Cs, totU, 238Pu, 239,240Pu, and 241Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of 90Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g‐1 [126E‐02 Bq kg‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g‐1 [518E‐02 Bq kg‐1]). The differences in 90Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y‐1 (1.0 ± 1.0 μSv y‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y‐1 (1000 μSv y‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.  相似文献   

16.
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.  相似文献   

17.
We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.  相似文献   

18.
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   

19.
A Natural Environment Research Council (NERC) funded Knowledge Transfer (KT) workshop was held in the United Kingdom (UK) to identify the needs and opportunities in the application of molecular biology and ‘omics’ techniques to environmental monitoring and risk assessment. Attendees highlighted a lack of effective communication between end-users and researchers as well as difficulties with data interpretation as reasons behind the slow uptake of molecular biology and omics techniques. A number of promising areas in which new techniques could be implemented at a practical level in the very near future were identified, thereby raising the profile of these recent technologies and providing vital proof of concept work. Molecular taxonomy, bacterial source tracking and pre-screening of chemicals for potential toxicities were all viewed as areas in which omics and molecular techniques could have immediate value, with the aim of reducing cost, increasing efficiency and providing more comprehensive data of improved quality.  相似文献   

20.
This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine~ amitrole~ simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log Kow) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.  相似文献   

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