短程硝化反硝化工艺处理低C/N餐厨废水

针对餐厨废水的水质特点,提出低C/N下的短程硝化反硝化餐厨废水处理组合工艺。通过控制微氧区、好氧区DO分别为0.5 mg/L和2.5 mg/L;硝化液,微氧区混合液和污泥回流比分别为200%、100%和100%,可以实现NO-2-N累积率达到90%以上,COD、氨氮平均去除率为73.42%和98.57%。较低的C/N使得反硝化效果不佳,对反应器进水补充适量的甲醇作为碳源,在COD/TN约为4的情况下,以NO-2-N为主的反硝化可以使反应器对TN的去除率达到94%,出水各项指标符合相关排放标准,实现了餐厨废水高效和经济的生物脱氮。     

养殖废水SBR碳源投加实时控制研究

畜禽养殖废水是典型的高氨氮、低C/N比有机废水。常规生物处理工艺由于反硝化碳源不足导致脱氮效率较低。在2个平行运行的序批式反应器(SBR)中建立实时控制体系以研究投加猪粪浓浆作为外部碳源对脱氮除磷效果的影响。结果表明,根据ORP实时曲线特征优化碳源投加方案,可按水质变化情况适量补充所需碳源,增强体系脱氮效果,同时加强对磷的去除。在优化碳源投加的运行期NH4+-N及PO43-的去除率分别达到99%和69%。     

碳源对静置/好氧/缺氧SBR脱氮除磷性能的影响

以合成废水为研究对象,分别以丙酸钠、乙酸钠/丙酸钠(1∶2碳/碳)、乙酸钠和葡萄糖为外加碳源,建立同步脱氮除磷的静置/好氧/缺氧序批式反应器(SOA-SBR)。通过比较长期运行过程中各反应器的脱氮除磷效果,考察不同碳源对静置/好氧/缺氧SBR脱氮除磷性能的影响,并通过分析典型周期内氮、磷元素及微生物体内储能物质的变化,探究其影响机理。结果表明,丙酸钠为碳源时SBR能获得96%的最佳除磷效果以及78.3%的总氮去除率;乙酸钠为单一碳源时可取得92.3%的除磷率和93.7%的总氮去除率;而混合碳源对于氮、磷的去除能力介于丙酸钠和乙酸钠之间;葡萄糖为单一碳源时系统对于磷和总氮的去除率仅26%和36.7%。丙酸钠和乙酸钠均能取得良好的同步脱氮除磷效果,但乙酸钠对总氮去除能力更佳。通过分析典型周期中内聚物含量变化表明,微生物体内聚羟基脂肪酸酯(PHA)和糖原质含量的变化与系统反硝化能力和溶解性正磷酸盐(SOP)去除效果呈正相关性。     

CAS-BT复合反应器同步脱氮除磷试验研究

在CAST反应器中引入自制悬浮填料,构成了CAS-BT复合反应器,采用人工配制废水,对其同步脱氮除磷效果进行了试验研究.试验结果表明,当TN为178.05 mg/L、TP为28.32 mg/L时,CAS-BT工艺取得了很好的同步脱氮除磷效果,TN和TP的去除率分别达到97.55%和98.10%.进行同步脱氮除磷时,CAS-BT比其他的水处理工艺更具优势.     

PCL-SND系统的脱氮效果

以处理水产养殖水体中的含氮化合物为目的,采用气提反应器,建立以聚己内酯(polycaprolactone,PCL)为碳源和生物膜载体的同时硝化反硝化(simultaneous nitrification and denitrification,SND)系统(PCL-SND),研究其启动过程及脱氮效果以及水力停留时间(hydraulic retention time,HRT)对PCL-SND系统脱氮效果的影响。结果表明,在PCL填充率为10%,HRT为24 h,进水氨氮(NH+4-N)浓度为10 mg/L,硝态氮(NO-3-N)浓度为50 mg/L的条件下,系统运行45 d达到稳定状态,NH+4-N和TN的去除率分别为(76.55±0.98)%和(56.85±2.21)%。HRT对PCL-SND系统脱氮效果的研究表明,一定范围内,TN去除率随着HRT的减小而下降,出水NO-3-N浓度随着HRT的减小而升高,当HRT8 h,NH+4-N去除率基本稳定(85%~89%),HRT为24 h时,脱氮效果最好,TN和NH+4-N去除率分别为(68.56±1.64)%和(87.75±2.78)%,出水NO-3-N浓度(15.72±1.46)mg/L。p H和总碱度均随HRT的减小而下降,生物量却随HRT的减小而增大。     

气升式环流生物膜反应器硝化反硝化除磷过程的研究

针对反硝化聚磷菌的生物学特性,设计并制作了硝化反硝化除磷气升式环流生物膜反应器,并就其对生活污水的脱氮、脱碳和除磷过程进行了试验.试验结果表明,当进水COD为309.8 mg/L、NH4 -N为116.0 mg/L、PO34-P为10.5 mg/L时,它们的去除率分别为95.3%、94.6%和73.1%.通过间歇试验表明该反应器可以实现反硝化除磷.     

(AO)_2SBR同步脱氮除磷的研究

以人工配水为研究对象,采用厌氧/好氧/缺氧/好氧交替运行的序批式反应器,研究了(AO)2SBR系统同步脱氮除磷的效果,并结合批式实验讨论了同步脱氮除磷的反应机理。研究结果表明,该系统以厌氧1.5 h、好氧1 h、缺氧3h、好氧0.5 h的方式运行,在DO=2.5 mg/L,SRT=15 d的条件下,具有良好的脱氮除磷效果,配水中的总氮、总磷、COD和总有机碳的去除率分别为96.26%、99.87%、90.46%和85.57%。批式实验表明,合成的内碳源越多,氨氮的硝化越充分,反硝化除磷越多。     

低曝气下PAC强化SBR工艺同步脱氮除磷

采用序批式反应器(SBR)处理模拟生活污水,研究不同曝气量(30、24、18和12 L/h)下活性污泥同步脱氮除磷规律,并在最佳曝气量下,比较了粉末活性炭-序批式反应器(PAC-SBR)和SBR的脱氮除磷效率,分析了低曝气下PAC-SBR的运行特性和优越性。实验结果表明,当曝气量为24 L/h时,SBR内出水效果较好,其COD、TN和TP的平均去除率分别可以达到90.02%、81.13%和88.12%。在这个最佳曝气量下,PAC-SBR具有明显的优势,其COD、TN和TP的平均去除率均高于SBR,并且PAC-SBR具有较好的污泥沉降性能和较高的活性污泥浓度。在PAC-SBR中,活性污泥以PAC作为微生物载体强化了生物降解效果,并改善了低曝气下污泥絮体的结构,促使反应器内先后形成缺氧-厌氧-微氧/缺氧-缺氧的环境,利于同步硝化反硝化和反硝化聚磷,提高了PAC-SBR的同步脱氮除磷效率。     

连续流反应器中培养好氧颗粒污泥的运行效能研究

在连续流完全混合反应器(CSTR)中,采用不同进水方式,以乙酸钠作为碳源配制的人工配水作为原水,对好氧颗粒污泥的运行效能进行了试验研究。研究表明,采用不同进水方式运行的2个反应器在颗粒污泥出现后,运行效能差别不大;好氧颗粒污泥反应器运行高效稳定,在水力停留时间为1.5h、COD容积负荷为1.0kg/(m3·d)的条件下,对COD、TP、NH4+-N和TN的去除率分别为90%、85%、95%和60%,并具有明显的脱氮除磷效果;反应器中存在同步硝化反硝化现象。     

一株耐盐好氧反硝化细菌的分离鉴定及其脱氮特性

从处理高盐废水的生物接触氧化工艺成熟活性污泥中分离得到一株耐盐好氧反硝化细菌F10.根据形态学特征、生理生化以及16S rRNA基因序列测定分析,初步判定该菌株为盐单胞菌属(Halomonas sp.).菌株能在盐度为3%~7%的培养基中良好的生长及脱氮,最适盐度为3%(以Na Cl计),最适碳源为乙酸钠,最适p H为7~8,最适温度为30℃.该菌株能利用NO-3-N进行反硝化作用,在盐度为3%的反硝化培养基中24 h内对NO-3-N的去除率达到92.6%,36 h基本完全去除。该菌株在3%盐度下表现出良好的异养硝化-好氧反硝化性能,初始硝态氮浓度在270 mg/L时,菌株的脱氮率可达90%以上,氨氮的去除率可达75%以上,脱氮过程中无NO-2-N积累,可实现同步硝化反硝化,具有一定的工程应用价值。     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and desorption behavior of chloroanilines and chlorophenols on montmorillonite and kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

Isocyanatocyclohexane and isothiocyanatocyclohexane levels in urban and industrial areas and possible emission-related activities

Isocyanatocyclohexane and isothiocyanatocyclohexane are becoming relevant compounds in urban and industrial air, as they are used in important amounts in automobile industry and building insulation, as well as in the manufacture of foams, rubber, paints and varnishes. Glass multi-sorbent tubes (Carbotrap, Carbopack, Carboxen) were connected to LCMA-UPC pump samplers for the retention of iso- and isothiocyanatocyclohexanes. The analysis was performed by automatic thermal desorption (ATD) coupled with capillary gas chromatography (GC)/mass spectrometry detector (MSD). TD-GC/MS was chosen as analytical method due to its versatility and the possibility of analysis of a wide range of volatility and polarity VOC in air samples. The method was satisfactory sensitive, selective and reproducible for the studied compounds. The concentrations of iso- and isothioisocyanatocyclohexanes were evaluated in different urban, residential and industrial locations from extensive VOC air quality and odour episode studies in several cities in the Northeastern edge of Spain. Around 200–300 VOC were determined qualitatively in each sample. Higher values of iso- and isothiocyanatocyclohexane were found in industrial areas than in urban or residential locations. The concentrations ranged between n.d.−246 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively, for industrial areas. On the other hand, urban and residential locations showed concentrations ranging between n.d.−164 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively. The site location (urban or industrial), the kind and nearness of possible iso- and isothiocyanatocyclohexane emission activities (industrial or building construction) and the changes of wind regimes throughout the year have been found the most important factors influencing the concentrations of these compounds in the different places.     

Degradation in soil and water and ecotoxicity of rimsulfuron and its metabolites.

The degradation and ecotoxicity of sulfonylurea herbicide rimsulfuron and its major metabolites were examined in batch samples of an alluvial sandy loam and in freshwater. An HPLC-DAD method was adapted to simultaneously identify and quantify rimsulfuron and its metabolites, which was successfully validated by GC-MS analysis. In aqueous solutions, pure rimsulfuron was rapidly hydrolyzed into metabolite 1 (N-(4,6-dimethoxypyrimidin-2-yl)-N-(3-(ethylsulfonyl)-2-pyridinylurea)), which itself was transformed into the more stable metabolite 2 (N-((3-(ethylsulfonyl)-2-pyridinyl)-4,6-dimethoxy-2-pyrimidineamine)), with half-life (t(1/2)) values of 2 and 2.5 days, respectively. Hydrolysis was instantaneous under alkaline conditions (pH = 10). In aqueous suspensions of the alluvial soil (pH = 8), formulated rimsulfuron had a half-life of 7 days, whereas that of metabolite 1 was similar to that in water (about 3.5 days). The degradation of the two major metabolites was also studied in soil suspensions with the pure compounds at concentrations ranging from 1 to 10 mg l(-1). The half-life of metabolite 1 ranged from 3.9 to 5 days, close to the previous values. Metabolite 2 was more persistent and its degradation is strongly dependent on the initial concentration (C0): half-life values ranged from 8.1 to 55 days at 2-10 mg l(-1), respectively. These values are higher than those determined from the kinetics of metabolite 1 transformation into metabolite 2 (t(1/2) = 8-19 days). The ecotoxicity of the three chemicals was evaluated through their effect on Daphnia magna and Vibrio fischeri (Microtox bioassay). No effect was observed on D. magna with 24 and 48 h acute toxicity tests. Similarly, no toxic effect was observed with the Microtox test for the three chemicals in the range of concentrations tested that included the field application dose. Thus, being of low persistence and lacking acute toxicity, these chemicals present a low environmental risk. However, chronic effects should be studied in order to confirm the safety of rimsulfuron and its major metabolites.