不同温度对SBBR同步短程硝化反硝化处理炼油催化剂废水的影响

采用SBBR在溶解氧1.0 mg/L条件下考察了不同温度对实际炼油催化剂废水脱氮系统效能的影响.结果表明,SBBR容积负荷及同步硝化反硝化(SND)三氮去除率与进水氨氮浓度正相关.不同进水浓度下,反应器SND三氮去除率最高可达40％左右.33、30及28℃条件下,反应器亚硝积累率均可稳定保持在90％以上.不同温度下短程硝化反硝化pH值及ORP变化趋势基本一致,结合在线监控pH值及ORP变化规律调控反应时间,最大限度保证短程硝化的稳定性.     

炭管膜曝气生物膜反应器SNAD脱氮研究

以包裹无纺布的微孔炭管作为膜曝气生物膜反应器（MABR）的膜组件，进行了短程硝化，厌氧氨氧化和反硝化耦合脱氮(SNAD)研究。实验中，控制温度34±1℃，pH 7.5～8.5, HRT 8 h，通过逐步降低膜内压力使反应器中的溶解氧由8 mg/L逐步降低到0.5 mg/L以下。实验采用亚硝酸细菌挂膜，然后接种厌氧氨氧化细菌，实现在单一反应器中同时发生短程硝化、厌氧氨氧化和反硝化耦合脱氮功能。结果表明，经过180 d的连续稳定运行，氨氮去除率达到了93.4%，总氮去除率达到了92.5%，COD去除率达到97.2%, 氨氮去除负荷0.6 kg N/（m³ ·d）。适合SNAD工艺的最佳C/N比为0.2～0.6，当COD浓度过高时，会抑制厌氧氨氧化细菌，使SNAD工艺的处理效果明显下降。     

同步硝化反硝化工艺中DO浓度对N2O产生量的影响

采用序批式生物膜反应器(SBBR),在连续曝气全程好氧的运行条件下,考察不同溶解氧浓度对同步硝化反硝化脱氮性能及N2O产量的影响.控制溶解氧浓度恒定在1、2、2.5和3 mg/L.结果表明,DO为2 mg/L和2.5 mg/L时,氨氮去除率分别为97.9%和98.5%,同步硝化反硝化率均为99%.DO为2 mg/L时,...     

溶解氧和有机碳源对同步硝化反硝化的影响

利用SBR反应器,探讨了溶解氧(DO)和有机碳源(COD)对同步硝化好氧反硝化的影响.结果表明,DO范围在0.5～0.6 mg/L时最适合于同步硝化好氧反硝化脱氮.在同步硝化反硝化过程中出现了亚硝酸盐氮的积累,推断经由短程硝化反硝化途径.总氮的去除率随着COD/N(碳氮比)的增加而增加,当COD/N为10.05时,总氮去除率最高可达70.39%.继续增加碳氮比时,总氮去除率增加不多,并且还会导致硝化作用不完全.当存在足够的易降解有机碳源时,能发生完全的好氧反硝化作用.     

膜生物反应器同步硝化反硝化系统的研究

设计结构合理的膜生物反应器,驯化培养硝化污泥,复配反硝化细菌,构建了具有同步硝化反硝化功能且能去除COD的膜生物反应器系统.MLVSS的增高和污泥结构的改善为同步硝化反硝化提供条件.进水氨氮浓度在50 mg/L,MLVSS为8 g/L时,最佳HRT为4～6 h,气量控制在0.5 m3/h左右,TN去除率达80%以上.系统承受负荷变化范围0～0.36 kg N/(m3·d),TN去除率均能保持80%左右,COD去除率稳定在90%.系统投加粉末活性炭的方法可以改善污泥结构,进而减轻膜污染.在试验阶段内,添加了PAC的活性污泥MLVSS的高低对膜通量的影响不大,膜通量基本保持稳定.     

同步硝化反硝化生物脱氮技术研究

讨论了影响同步硝化反硝化反应的各参数,并进行了单因素实验与正交实验,获得了同步硝化反硝化生物脱氮工艺运行的最佳条件:DO浓度控制在0.5～2 mg/L,COD浓度为600～800mg/L,混合液悬浮固体(MLSS)为5000 mg/L,pH值在8.0左右,反应时间为6 h.在此条件下,氨氮及COD的去除率都较高,分别达85%和95%,总氮去除率为68 5%.     

DO对好氧颗粒污泥短程同步硝化反硝化脱氮的影响

以模拟城市污水为处理对象，研究了不同溶解氧下序批式活性污泥反应器（SBR）的短程同步硝化反硝化过程特征及处理效果。试验结果表明，溶解氧浓度是实现短程同步硝化反硝化的一个重要控制参数。在亚氮积累阶段，控制温度为28～32℃，pH值为7.5～7.8，当进水NH⁺₄-N为30 mg/L左右，COD为250 mg/L左右时，亚硝酸盐氮的积累率达到96%～98%。在试验阶段，常温下控制溶解氧在0.5～1.0 mg/L，可保证氨氮的去除率达到95%～97%，总氮的去除率达到82%～85%。     

固定化活性污泥实现短程硝化反硝化处理畜禽废水

以畜禽废水为处理对象,通过分别控制水力停留时间(HRT)、溶解氧(DO)、pH值、温度和碳氮比(C/N)等影响亚硝化的主要单因子,以使固定化活性污泥颗粒实现短程硝化反硝化反应,在连续流运行模式下进行废水脱氮实验,实验结果表明,单因子HRT为10 h,溶解氧为4 mg/L,pH值为8.5,温度为30℃,碳氮比为10时,对TN和COD的去除率分别为81.98%、93.79%;87.32%、98.35%;83.82%、93.93%;85%、97%;85.37%、97.28%,达到了理想的去除效果。     

泥炭作为缓释碳源对反硝化过程的影响

采用柱实验,以泥炭颗粒作为缓释碳源,探究不同水力停留时间(HRT)下泥炭颗粒对反硝化过程的影响。结果表明:(1)泥炭颗粒可作为有效缓释碳源,当HRT为6.67h时,脱氮效果最好,硝酸盐氮去除率能达到81.9%。(2)出水COD较低,最终为9～12mg/L,不会对水体造成二次污染;亚硝酸盐氮先升后降,最终均小于0.2mg/L,未出现积累现象,泥炭颗粒可作为生物脱氮反应器中长期运行的缓释碳源。     

生物膜反应器中低氨氮浓度废水的亚硝化

在连续流生物膜反应器中通过控制DO、pH和HRT,对低氨氮浓度废水进行了亚硝化的实验研究。结果表明,在进水氨氮浓度为35～45 mg/L,温度为34℃的情况下,当DO=1.4～1.5 mg/L,pH=8.3,HRT=6 h时,氨氮的去除率与亚硝态氮的积累率均可达到80%左右,实现了较好的氨氮降解及稳定的亚硝态氮的积累。     

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.     

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.     

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.     

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.     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.     

Synthesis and characterization of m- and p-methylbenzyl-mercapturic acids derived from m- and p-xylenes

Chemical synthesis and physical properties of two mercapturic acids suggested as urinary metabolites of m- and p-xylenes ace described. These compounds may be used for the identification and quantivative determination by high-performance liquid chromatography of the corresponding mercapturic acids in urine.     

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。