添加堆肥和赤泥对土壤生物有效性Cd和Zn的影响

采用土壤培养实验,研究添加堆肥和赤泥对土壤中Zn和Cd生物有效性的影响。结果表明,单独添加堆肥或赤泥以及赤泥和堆肥一起添加到土壤,均可以降低土壤中的交换态Cd和Zn含量以及生物有效态Zn和Cd含量。与对照相比,培养1~3个月后,单独添加堆肥、单独添加赤泥和同时添加赤泥与堆肥导致土壤交换态Cd含量分别降低14%~18%、33.3%~46.1%和44.2%~57.7%;土壤交换态Zn含量分别降低54.4%~59%、100%和100%;土壤生物有效态Cd含量分别降低11.8%~14.7%、25.1%~33.7%和32.6%~43.9%;土壤生物有效态Zn含量分别降低14.1%~15.8%、59.7%~72.2%和43.2%~58.4%。     

高温堆肥与蚯蚓堆肥对城市污泥重金属形态的影响

采用高温堆肥和蚯蚓堆肥工艺,研究了城市污泥与锯末、粉煤灰或磷矿粉按不同比例混合堆肥前后重金属（Cu、Pb、Zn、Cd和As）交换态、碳酸盐结合态、铁锰氧化物结合态、有机结合态和残留态的变化。研究表明：高温堆肥和蚯蚓堆肥前后各试验污泥的重金属形态和含量呈现出不同的变化,都可以降低污泥中交换态Cu、Pb、Zn、Cd和As的含量;对于Cu和Pb,高温堆肥优于蚯蚓堆肥;对于Zn、Cd和As,蚯蚓堆肥优于高温堆肥。2种堆肥方式中,粉煤灰用量为10%的钝化效果优于20%,磷矿粉的钝化效果同粉煤灰一样。     

改性沸石对土壤铅、锌赋存形态的影响简

通过室内土壤培养实验,研究改性沸石对污染土壤中Pb、Zn赋存形态的影响。结果表明,土壤中的Pb主要是以Fe-Mn氧化物结合态存在,土壤Zn主要以残渣态存在。添加天然沸石和改性沸石不同程度地降低土壤酸提取态Pb、Zn的含量,提高土壤残渣态Pb、Zn的含量。与CK处理相比,添加4种沸石导致土壤酸提取态Pb含量降低8.7%~40.3%,土壤酸提取态Zn含量降低10.5%~49.8%（培养1个月）。硝酸钾改性沸石比天然沸石更能显著地降低土壤酸提取态Pb、Zn的含量,而氢氧化钠改性沸石和硝酸钾改性沸石比天然沸石更能显著地降低土壤酸提取态的Zn含量。培养1、2和3月后,不同沸石处理导致土壤残渣态Zn比率分别比CK处理提高14.4%~23.5%、19.6%~23.7%和1.9%~11.1%。研究结果表明,天然沸石经过一定方法改性后,是固定污染土壤Pb、Zn的潜在改良剂。     

氯化铁和硫酸铁对酸性土壤中有效态镉和铅污染的修复作用

采用浸泡实验法研究了氯化铁和硫酸铁对酸性土壤中有效态镉和铅污染的修复效果,结果表明,氯化铁和硫酸铁均能有效去除土壤有效态镉和铅污染,Fe(Ⅲ)用量为50～100 mmol/kg时,有效态Cd和Pb的去除效果可达70％～96％.氯化铁和硫酸铁能去除土壤中的水溶态、碳酸盐结合态、腐殖酸结合态、铁锰氧化物结合态和强有机结合态Cd和Pb及交换态Cd.氯化铁和硫酸铁对Cd均既有洗脱修复作用又有固定修复作用,且洗脱修复作用的贡献稍大;氯化铁用量较小时(50 mmol/kg)对Pb既有固定修复又有洗脱修复作用,固定修复作用稍大;用量较大时(100 mmol/kg),对Pb只有洗脱修复作用.硫酸铁对Pb的修复作用则以固定修复作用为主,洗脱修复作用很小.     

金矿区高浓度砷污染土壤的稳定化处理

以粉煤灰、干化污泥、粉碎花生壳、硫酸亚铁(Fe_2SO_4)和磷酸二氢钾(KH_2PO_4)为稳定剂对矿区高浓度As污染土壤进行处理,通过土壤理化性质、重金属形态和浸出浓度变化等综合评估稳定剂对高浓度砷污染土壤的稳定化处理效果。结果表明,添加稳定剂可以提高土壤pH值、有机质含量和阳离子交换量。粉煤灰、干化污泥、粉碎花生壳、硫酸亚铁对土壤中的As有较好的稳定化作用,其中硫酸亚铁对土壤中As的稳定效果最好。同时添加10%粉煤灰、10%干化污泥和1%硫酸亚铁后,土壤中可交换态As、碳酸盐结合态As、铁锰氧化物结合态As、有机结合态As含量显著降低,降幅分别为62.3%、55.2%、29.6%、58.2%,残渣态As含量增加8.1%。添加粉煤灰、干化污泥、硫酸亚铁能显著降低土壤中As的浸出浓度,而添加KH_2PO_4会使土壤中As浸出浓度增加,移动性增强。当同时添加10%粉煤灰、10%干化污泥、1%粉碎花生壳和1%硫酸亚铁后,As浸出浓度最低(0.93 mg·L~(-1)),稳定效果最好,稳定化效率达到了74.8%。土壤中As的浸出浓度与可交换态As和碳酸盐结合态As呈显著正相关,与残渣态As呈显著负相关,可交换态As、碳酸盐结合态As和残渣态-As含量是影响土壤中As浸出浓度变化的主要因素。     

改性沸石对土壤铅、锌赋存形态的影响

通过室内土壤培养实验,研究改性沸石对污染土壤中Pb、Zn赋存形态的影响。结果表明,土壤中的Pb主要是以Fe—Mn氧化物结合态存在,土壤zn主要以残渣态存在。添加天然沸石和改性沸石不同程度地降低土壤酸提取态Pb、zn的含量,提高土壤残渣态Pb、zn的含量。与CK处理相比,添加4种沸石导致土壤酸提取态Pb含量降低8．7％-40．3％,土壤酸提取态zn含量降低10．5％-49．8％（培养1个月）。硝酸钾改性沸石比天然沸石更能显著地降低土壤酸提取态Pb、zn的含量,而氢氧化钠改性沸石和硝酸钾改性沸石比天然沸石更能显著地降低土壤酸提取态的zn含量。培养1、2和3月后,不同沸石处理导致土壤残渣态zn比率分别比CK处理提高14．4％～23．5％、19．6％～23．7％和1．9％-11．1％。研究结果表明,天然沸石经过一定方法改性后,是固定污染土壤Pb、zn的潜在改良剂。     

餐厨垃圾与铬污染土壤混合堆肥中铬形态的转化

进行了不同比例铬污染土壤与餐厨垃圾混合堆肥实验,分析了堆肥过程铬形态的变化、浸出液毒性以及种子发芽指数.结果表明,堆肥实验后,堆肥物料中可交换态和碳酸盐结合态的铬含量逐渐减少,最多可分别减少82.6%和72.69%,有机结合态的铬含量明显增加,最大增幅为106.58%;堆肥物料浸出液铬的浓度低于国家危险废物鉴别标准,浸...     

公路两侧土壤中铅和镉污染以及存在形态分布的分析

测定了土壤中铅、镉总量,并采用五级连续浸提法和石墨炉原子吸收分光光度法对北京市3条典型公路两侧的土壤样品中铅和镉的存在形态分布进行了测定.结果表明,所选3条公路出京方向右侧的土壤铅和镉污染严重,其铅、镉总量分别是北京地区土壤铅和镉含量背景值的1.62～6.69、5.97～18.74倍.土壤中铅主要以铁锰氧化物结合态、碳酸盐结合态、有机结合态和残渣态等形式存在,镉主要以铁锰氧化物结合态和残渣态形式存在,而活性强的离子交换态浓度均较低.不容忽视的是,铅和镉的碳酸盐结合态在碱性条件下稳定,但是具有遇酸释放的隐患.     

冻融循环及有机肥配施对黑土中镉形态的影响

以黑龙江黑土为对象,研究了冻融循环及有机肥配施量对黑土中镉形态分布的影响。对配施不同有机肥的土壤样品进行5次冻融循环,采用电感耦合等离子质谱仪(ICP-MS)分析土壤样品中镉的赋存形态。结果表明,冻融循环数及有机肥的配施有助于降低黑土中的总镉量;冻融循环会促使黑土中的镉由交换态、碳酸盐结合态、有机结合态向铁锰氧化物结合态和残渣态转化,而增加有机肥配施量会使黑土中的镉由交换态向其他形态转化。因此,冻融循环及有机肥配施有助于降低土壤中镉的生物有效性,进而降低其环境风险。     

氮肥对污染农田土壤中铅的调控效应

用铅污染农田土壤做盆栽试验,研究了氮肥品种和施用量对小白菜吸收铅及土壤中铅形态的影响.结果表明,在氮肥施用量相同的条件下,施用不同形态氮肥对小白菜地上部及根系吸收铅有显著影响;适量的NH4NO3不会对小白菜地上部造成显著影响,增施Ca(NO3)2也不会造成小白菜地上部含铅量的继续增加;各施氮处理的土壤pH较不施氮处理的土壤pH均有不同程度的降低,且以(NH4)2SO4处理的土壤pH下降幅度最大,施用Ca(NO3)2的处理的土壤pH变化不显著;氮肥在一定程度上会影响土壤中各形态含铅量,其中对交换态、碳酸盐结合态、无定形氧化锰结合态,无定形氧化铁结合态及有机结合态含铅量影响较大,但并未改变各形态铅的分布顺序;小白菜吸收的铅主要来源于土壤中的交换态铅,但也可吸收部分碳酸盐结合态铅、铁锰氧化物结合态铅及有机结合态铅,甚至可吸收部分残渣态铅.     

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。     

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.     

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。     

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.     

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.     

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.     

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.