高效阿特拉津降解菌株DNSIO降解条件优化

从长期施用阿特拉津的寒地黑土耕层（0～10cm）土壤中筛选到一株能以除草剂阿特拉津为氮源生长的降解菌株，结合16SrRNA序列分析结果，将该菌株命名为Arthrobacter sp．DNSl0。在接种量为10。CFU／mL的条件下，菌株DNSl0在24h内对100mg／L阿特拉津的降解率为99．41％。单因子实验结果表明，菌株DNSl0适宜生长和降解的条件范围是：温度25～35＇12，pH值5．0～8．0，培养液盐度0．1％～2％，对阿特拉津最大耐受浓度可达1200mg／L。正交实验法进一步表明，该菌株保持较好生长及降解能力的最优方案是温度30℃，pH值7．5，培养液盐度0．5％。影响其降解能力的环境因素的主次顺序依次是：温度〉盐度〉pH值。     

高效石油烃降解菌SKD-1的分离、筛选及其降解性能

从孤岛油田石油污染土壤中分离到一株高效石油降解菌，命名为SKD-1。该菌株菌落表面湿润光滑、边缘整齐、圆形、不透明、乳黄色，能够利用葡萄糖和淀粉作为其生长的碳源和能源，其最适生长环境为碱性（pH8-10），在分别以正十六烷烃和原油为惟一碳源，温度为30℃，摇床（180r／min）培养的条件下，菌株SKD-1的降解率分别为66．1％和36．9％。16SrRNA基因序列分析表明，菌株SKD-1与不动杆菌AcinetobactercalcoaceticusSY-1同源性达99％。结合菌株SKD．1菌落形态、理化性质以及系统发育分析，可以鉴定菌株SKD-1属于不动杆菌属（Acinetobactersp．），序列登录号为AB774229。     

烟酰胺降解菌的筛选及其降解特性

采用HPLC对某烟酰胺生产废水的主要成分进行分析，并模拟废水中的主要成分烟酰胺（nicotinamide）的浓度，对以烟酰胺为唯一碳源配制的培养基进行降解实验，获得有较佳降解率和生长能力的菌株YSI-1和YSI-2。结果表明．YSI菌株的混合菌降解效果优于单株菌，混合菌在初始OD600值为0．4，pH为7．0时，对浓度为2000mg／L的烟酰胺降解2d的降解率可达32．8％。延长处理时间或提高菌种的初始OD600值，烟酰胺的去除率均有较大的增加。     

耐酸厌氧消化污泥处理餐厨垃圾

采用耐酸驯化的厌氧消化污泥处理餐厨垃圾，在酸性条件下（pH=4．5），对实验装置容积负荷从1．0kgVS／（m3·d）分9次逐级增加到5．0kgVS／（m3·d）的过程进行了跟踪监测，并较深入地研究了驯化污泥代谢活性和处理效果。实验结果表明，pH4．5的耐酸厌氧消化污泥，最佳投加负荷约为4．5kgVS／（m3·d），此负荷下容积产气率，CH4含量平均值均达最大，分别为1．68m3／（m3·d），75．0％。耐酸厌氧消化装置持续增料运行46d，产甲烷菌仍能保持较高的活性，其COD去除率范围为40．4％-75．0％，仍能保持pH7．2时处理效果的65．0％-91．8％，表明在低pH、低碱度下实现稳定的产甲烷过程是可行的。     

TA高效降解菌株培养基的优化

对TA高效降解菌株的生长培养基进行了5因素2水平标准的正交设计，考察了碳源（精对苯二甲酸PTA）、氮源（NH4Cl）、磷源（K2HPO4）、生长因子（MgSO4、FeSO4、CaCl2的混合物）和酵母膏对菌体生长的影响。并与肉汤培养基相对照，得到TA高效降解菌株生长培养基为：PTA10g／L；NH4Cl 0．5g／L；K2HPO4 0．1g／L；生长因子（MgSO4 0．1g／L，FeSO4 0．01g／L，CaCl2 0．01g／L的混合物）；Y．E2．5g／L。     

高盐废水盐度对中度嗜盐菌生长动力学的影响

高盐废水盐度变化是影响微生物生长的重要因素之一。研究以中度嗜盐菌Halomonassp．STSY．3为例，测定其在不同盐度下生长对数期末OD600,并以葡萄糖为限制性基质，利用Monod方程，对菌株进行生长动力学拟合。结果表明，Halomonassp．STSY-3的最适生长盐度为7％（以NaCl计），此盐度下其OD600 为2．56，而0%和34％盐度下OD600分别为0．47和0．06；Halomonassp．STSY-3的生长动力学模型与实验数据能较好地拟合，在最适生长盐度下动力学模型参数μmax 为2．257h-1，Ks为0．0082g／L。比较不同盐度下STSY-3生长动力学参数，得出中度嗜盐菌STSY-3的生长存在3个明显分区：最适盐度区（盐度2％～9％）、嗜盐过渡区（盐度9％～20％和0．68％～1．76％）及生长抑制区（盐度≤2％或≥20％）。其中嗜盐过渡区0．68％～1．76％由于范围较小，实际意义小，忽略不计。     

Fe^o／厌氧微生物体系降解2，4，6-三氯酚特性研究

通过摇床间歇实验，研究了厌氧微生物与零价铁（Fe^o）联合体系降解2，4，6-三氯酚（TCP）的特性，结果表明，在pH7．5，35℃，150r／min，Fe^o10g／L条件下，TCP初始浓度为30mg／L时，TCP降解的拟一级反应速率常数为0．0207h～，添加少量碳源可达到0．0390h^-1，其降解速率是前者的1．88倍；添加碳源的体系在220h内连续多次投加TCP降解率都达到80％以上，而不加碳源的体系在第2次投加TCP后降解率就只有30％左右；添加不同碳源，降解速率不同；添加2-溴乙烷磺酸钠（BESA）以及SO4^2-、NO3^-和S^2-对TCP降解有不同的抑制作用。     

不同pH下水葫芦与紫根水葫芦生长特性与净化效能对比研究

为了探讨不同pH条件下水葫芦与紫根水葫芦生长特性与净化效能的差异，以滇池草海原水为实验用水，利用HCl和NaOH稀溶液调节水体pH，设置3个pH处理，分别是8．00、9．50和11．00，开展了为期30d（重复3个周期）的静态模拟实验，结果表明，在实验条件下，pH过高会对水葫芦和紫根水葫芦的生长发育产生抑制作用，紫根水葫芦受到的抑制效果更为明显；水葫芦和紫根水葫芦的生长也会使水体pH降低至接近中性，水葫芦调节水体pH的能力更强；pH为8．00、9．50时，水葫芦和紫根水葫芦对水体氮磷污染物具有净化作用，水葫芦的净化能力更强；pH为11．00时，水葫芦和紫根水葫芦处理的水体氮磷浓度均表现起伏，表示在高碱度条件下，两者的净化能力减弱。     

温度对复合厌氧折流板膜生物反应器处理生活污水效能的影响

将新型CAMBR反应器（厌氧折流板反应器（ABR）与膜生物反应器（MBR）优化组合）用于处理生活污水，研究温度对该反应器处理效能的影响。实验水力停留时间7．5h，混合液回流比设置为200％，pH值为6．5～8．5，溶解氧3mg／L左右。控制3个温度梯度：高温（32～37％），中温（20～25℃），低温（5～10％），每个温度运行35d。结果表明，在高温条件下，系统出水COD、NH4．N、TN和TP平均浓度分别为25、0．5、12．5和0．7mg／L。在中温条件下，系统出水COD、NH4＋-N、TN和TP浓度分别30、1．2、12．5和0．4mg／L。在低温条件下，COD和TP分别经过15d和20d调整适应，出水可恢复至35mg／L和1mg／L。由于低温（10％以下）对硝化细菌产生强烈抑制，出水NH4＋-N去除率最终稳定在35％，TN去除率为40％。低温条件下，该反应器应用于污水处理中需注意适当保温，以保证出水水质。     

氐温喹啉降解菌的筛选及降解性能

从吉林石化污水处理厂的活性污泥中驯化、筛选获得一株降解效率高且生长速率快高效耐冷菌，命名为WS-5。该菌能以喹啉作为惟一的碳源、氮源及能源。结合菌体的形态观察、生理生化特性实验及16SrDNA序列同源性对比分析，鉴定菌株WS-5为恶臭假单胞菌（Pseudomonasputida）。不同降解条件下的实验结果表明，菌株WS-5的最佳降解条件是投菌量为15％，pH值范围在8～10，摇床转速为100r／min。最佳降解环境下对200mg／L的喹啉在132h降解率达到了85．3％。菌株WS-5对初始喹啉浓度为50、100、200和300mg／L的初始喹啉浓度分别在36、72、192和262h内完全降解。这将为今后在低温条件下处理含喹啉废水提供技术指导。     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.     

Quantification of carbamazepine and atrazine and screening of suspect organic contaminants in surface and drinking waters

A new approach for the identification of suspect trace organic contaminants in drinking and surface waters is presented. Samples were initially analyzed using a target determination method for two contamination tracers, carbamazepine (CBZ) and atrazine (ATZ). This method used offline solid-phase extraction and online solid-phase extraction techniques coupled to liquid chromatography-triple quadrupole mass spectrometry to accelerate the sample preparation process and improve method performance. CBZ and ATZ were found respectively in 31% and 56% of the samples, and concentrations were usually <20 ng L⁻¹. These samples were re-analyzed with a similar method on a quadrupole time-of-flight mass spectrometer to identify suspect contaminants by means of exact mass measurements and isotope patterns. A database of 264 common organic contaminants was built and used in conjunction with a Molecular Feature algorithm to identify the presence of these substances in drinking and surface water collected from different sources at various locations across Canada. Several organic contaminants were identified in the samples, but only the presence of caffeine, desethylatrazine, simazine and venlafaxine could be verified by comparison to pure standards. The presence of desethylatrazine was also confirmed by MS/MS experiments. These results suggest that target analysis for tracers of organic contamination may be a helpful tool to prioritize samples which should be further screened for suspect contaminants. This study also shows that the combination of separation techniques (offline and online SPE, LC) contribute to advance the applicability of high-resolution mass spectrometry for the identification of trace organic contaminants by accelerating the preparation step, reducing complexity and increasing analyte concentrations for optimal detection.     

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.     

剩余污泥浓缩脱水投药量优化和模型建立

应用高分子阳离子絮凝剂（CPF-100）和聚丙烯酰胺（PAM）对污水厂剩余污泥进行浓缩脱水实验，研究表明：CPF-100的浓缩脱水效果优于PAM；当CPF-00投加量为1．16‰时，污泥沉降性能改善程度为37．51％；且在CPF-100投加量逐渐增大的初始阶段，污泥沉降性能改善程度随投加量的增加而增大，但CPF-100投加量也不宜过大，当CPF-100投加量超过1．16‰后，反而会使浓缩脱水效果变差。同时，建立了污泥沉降性能改善程度与絮凝剂CPF-100投加量、沉降时间之间的数学模型，其能较好地反映污水厂剩余污泥的浓缩脱水效果。     

Effects of compositional heterogeneity and nanoporosity of raw and treated biomass-generated soot on adsorption and absorption of organic contaminants

A biomass-generated soot was sequentially treated by HCl-HF solution, organic solvent, and oxidative acid to remove ash, extractable native organic matter (EOM), and amorphous carbon. The compositional heterogeneity and nano-structure of the untreated and treated soot samples were characterized by elemental analysis, thermal gravimetric analysis, BET-N₂ surface area, and electron microscopic analysis. Sorption properties of polar and nonpolar organic pollutants onto the soot samples were compared, and individual contributions of adsorption and absorption were quantified. The sorption isotherms for raw sample were practically linear, while were nonlinear for the pretreated-soot. The removal of EOM enhanced adsorption and reduced absorption, indicating that EOM served as a partitioning phase and simultaneously masked the adsorptive sites. By drastic-oxidation, the outer amorphous carbon and the inner disordered core of the soot particles were completely removed, and a fullerene-like nanoporous structure (aromatic shell) was created, which promoted additional π-π interaction between phenanthrene and the soot.     

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.