高效生物活性炭吸附工艺去除水体中甲基叔丁基醚的初步研究

通过对来自美国加州拉玛达(La Mirada)市污染点的原始菌源炭进行甲基叔丁基醚(MTBE)降解菌生物强化,试图建立具有更有效MTBE降解效果的生物活性炭(BAC)功能,尝试利用新形成的菌源炭覆盖新鲜椰壳活性炭(GAC)而达到新BAC功能的快速有效启动,并考察不同空床停留时间(EBCT)、GAC吸附饱和状态对BAC功能启动的影响。同时,对具有成熟BAC功能的炭柱中的混合菌落进行基于16SrDNA的聚合酶链反应(PCR)—变性梯度凝胶电泳(DGGE)分析,以确定混合菌落中的主要功能菌种属。结果表明,针对模拟的低MTBE浓度进水,新鲜GAC和菌源炭A添加体积分数分别为40%和60%的NAS柱出水MTBE质量浓度最终稳定低于0.005mg/L,平均去除率接近99%,出水MTBE完全达到美国环境保护署(EPA)的饮用水建议阈值(<20μg/L),建立了成熟的BAC功能;成熟的菌源炭可在30d左右通过覆盖法迅速实现新BAC功能的启动;EBCT的延长有利于新BAC功能的启动和维持,接种初期应尽量采用较长EBCT以保证取得足够和稳定的生物量;MTBE吸附饱和前后的GAC在启动新BAC功能时存在差异,鉴于吸附饱和GAC在接种初期会因MTBE解吸而造成出水MTBE浓度较高,建议采用新鲜活性炭覆盖需接种炭柱;BAC功能成熟炭柱中包括的5种主要菌种里有4种为未培养微生物,1种为未分类菌种,其理化性质和具体属性尚不明确。     

Carbon and hydrogen isotope effects during sorption of organic contaminants on carbonaceous materials

Stable carbon and hydrogen isotopes can be an efficient means to validate biodegradation of organic contaminants in groundwater since it results in an isotopic fractionation. A prerequisite in applying this method in the field is the proof that other processes decreasing the contaminant concentration are conservative with respect to isotope effects. In this paper we show for carbon isotopes of halogenated hydrocarbon compounds [trichloroethene (TCE), cis-dichloroethene (c-DCE), vinylchloride (VC)] and carbon and hydrogen isotopes of BTEX compounds (benzene, toluene, p-xylene) that no significant fractionation occurs during equilibrium sorption onto activated carbon, lignite coke and lignite. In general, effects were in the range of the reproducibility limit of the analytical instrument (0.5 per thousand for delta13C, and 8 per thousand for delta2H). This observation was made for fractions sorbed of less than 5% to more than 95%. Also for rate-limited sorption of TCE onto activated carbon, no significant fractionation in carbon isotopes could be observed. These findings support the assumption that for these classes of compounds, sorption processes in aquifer systems are conservative with respect to isotope effects.     

Distribution and fractionation of heavy metals in the Tisa (Tisza) River sediments

Introduction In this work, sediments of the River Tisa (Tisza) are studied to assess their environmental pollution levels for some major heavy metals, as well as to predict the investigated elements’ mobility on the basis of their association type with the substrate. The Tisa River catchments area is a subbasin of the River Danube. Part of this river, 166 km long, belongs to the Serbian province of Vojvodina, before it flows into the Danube. It has been chosen for our investigation, because it has been exposed to intense pollution in the last decades. Materials and Methods The river sediment samples were collected at 32 locations. The proportions of sand, silt and clay fractions were determined. The sequential extraction procedure following a modified Tessier method was applied for speciation of the metal forms in the collected samples. The metal concentrations of Zn, Cd, Pb, Ni, Cu, Cr, Fe and Mn in extracts were determined by atomic absorption spectroscopy. Results and Discussion Granulometric analysis showed that some 50% of the Tisa River sediments were silt and clay, while the rest was sand with quartz, as the main constituent. The average metal content of the surface river sediment samples for every fraction of sequential extraction was presented and discussed in relation to pH, Eh and metal fractionation. The average metal content from the Tisa River sediments, obtained as an average of the metal’s concentration released in all five sequential extraction fractions was compared with: average metal contents of the Tisa River sediments in Hungary, metal content in soils formed on the Tisa River alluvium of Vojvodina, average metal content in soils of Vojvodina, and average metal content in soils of Hungary. An assessment of metal pollution levels in Tisa River sediments was made by comparing mean values for obtained results for the Tisa River sediments with the freshwater sediment’s Quality Guidelines as published by US EPA, Environment Canada and soil standards for Serbia. Conclusion According to US EPA and Canadian Quality Guidelines for freshwater sediments, the concentration of heavy metals in Tisa sediments were: (a) much higher than defined concentrations below which harmful effects on river biota are unlikely to be observed, (b) below defined concentrations above which harmful effects on river biota are likely to be observed. The concentration levels of Pb, Ni, Cu and Cr in Tisa River sediments are safe when compared with Serbian MAQ (Maximum Allowed Quantity) standards for soils, but they are unsafe in the case of Zn and Cd. Recommendations and Outlook The quality of sediments in the Tisa River was on the border line between potentially polluted and polluted. This line could very easily be exceeded since the quality of sediments in the Tisa River in Hungary was already worse than in Serbia. These results indicated the need for further monitoring of heavy metals in that locality.     

Fractionation and mobility of phosphorus in a sandy forest soil amended with biosolids

Goal, Scope and Background Biosolids, i.e., treated sewage sludge, are commonly used as a fertilizer and amendment to improve soil productivity. Application of biosolids to meet the nitrogen (N) requirements of crops can lead to accumulation of phosphorus (P) in soils, which may result in P loss to water bodies. Since 1996, biosolids have been applied to a Pinus radiata D. Don plantation near Nelson City, New Zealand, in an N-deficient sandy soil. To investigate sustainability of the biosolids application programme, a long-term research trial was established in 1997, and biosolids were applied every three years, at three application rates, including control (no biosolids), standard and high treatments, based on total N loading. The objective of this study was to evaluate the effect of repeated application of biosolids on P mobility in the sandy soil. Materials and Methods Soil samples were collected in August 2004 from the trial site at depths of 0–10, 10–25, 25–50, 50–75, and 75–100 cm. The soil samples were analysed for total P (TP), plant-available P (Olsen P and Mehlich 3 P), and various P fractions (water-soluble, bioavailable, Fe and Al-bound, Ca-bound, and residual) using a sequential P fractionation procedure. Results and Discussion Soil TP and Olsen P in the high biosolids treatment (equivalent to 600 kg N ha⁻¹ applied every three years) had increased significantly (P<0.05) in both 0–10 cm and 10–25 cm layers. Mehlich 3 P in soil of the high treatment had increased significantly only at 0–10 cm. Olsen P appeared to be more sensitive than Mehlich 3 P as an indicator of P movement in a soil profile. Phosphorus fractionation revealed that inorganic P (Al/Fe-bound P and Ca-bound P) and residual P were the main P pools in soil, whereas water-soluble P accounted for approximately 70% of TP in biosolids. Little organic P was found in either the soil or biosolids. Concentrations of water-soluble P, bioavailable inorganic P (NaHCO₃ Pi) and potentially bioavailable inorganic P (NaOH Pi) in both 0–10 and 10–25 cm depths were significantly higher in the high biosolids treatment than in the control. Mass balance calculation indicated that most P applied with biosolids was retained by the top soil (0–25 cm). The standard biosolids treatment (equivalent to 300 kg N ha⁻¹ applied every three years) had no significant effect on concentrations of TP, Mehlich 3 P and Olsen P, and P fractions in soil. Conclusions The results indicate that the soil had the capacity to retain most biosolids-derived P, and there was a minimal risk of P losses via leaching in the medium term in the sandy forest soil because of the repeated biosolids application, particularly at the standard rate. Recommendations and Perspectives Application to low-fertility forest land can be used as an environmentally friendly option for biosolids management. When biosolids are applied at a rate to meet the N requirement of the tree crop, it can take a very long time before the forest soil is saturated with P. However, when a biosolids product contains high concentrations of P and is applied at a high rate, the forest ecosystem may not have the capacity to retain all P applied with biosolids in the long term. ESS-Submission Editor: Dr. Jean-Paul Schwitzguébel jean-paul.schwitzguebel@epfl.ch     

土壤铜形态和生物有效性对施用生物质炭的响应

采用改进的Tessier方法对土壤Cu形态进行分级,研究了添加生物质炭对土壤重金属Cu形态、生物有效性和小麦生长及生理指标的影响。结果表明,石灰性土壤中Cu主要以碳酸盐结合态、氧化态和残渣态形式存在,三者占土壤Cu的90%以上。添加生物质炭后,土壤中的碳酸盐结合态铜、氧化态铜含量有所减少,但不显著;有机物结合态铜含量增加了131.25%,达到极显著水平,其中主要增加了紧有机结合态。添加生物质炭在培养一定时间后（30 d后）土壤有效态铜含量降低,120天时最大降低幅度达50.66%,添加生物质炭提高了冬小麦的根系重、茎秆干重、籽粒干重和灌浆期旗叶叶绿素含量,降低了根系、茎秆和籽粒的含铜量以及超氧化物歧化酶（SOD）活性,并随着生物质炭施用量的增加有显著性差异。综合看来,生物质炭对土壤铜污染具有钝化作用。     

Soil pH and Anion Abundance Affects on Copper Adsorption

Abstract

Copper (Cu) input to agricultural soils results from Cu containing pesticides and/or that in soil amendments, such as manure or sewage sludge. Soil and soil solution properties influence the adsorption and desorption of Cu by the soil, which in turn determines its plant availability and/or phytotoxicities. Effects of different anion enrichment in the equilibrium solution on Cu adsorption by different soils (pH range of 6.2–9.9) were investigated in this study over a range of Cu concentrations. With Cu concentrations in the range of 0–100 mg L^?1 in the equilibration solution, 95–99% of applied Cu was adsorbed by all three soils. The adsorption of Cu was similar regardless of using either 0.01 M CaCl₂ or Ca(NO₃)₂ as the equilibration solution. When the Cu concentration in the equilibration solution was further increased in the range of 500–2000 mg L^?1, the adsorption of Cu decreased from 60 to 24% of applied Cu in two soils with pH 6.2–7.9. In a high pH soil (pH = 9.9), the Cu adsorption decreased from 77 to 34%. Addition of incinerated sewage sludge (ISS) to a Palouse silt loam soil (pH = 6.2) increased the Cu adsorption as compared to that by unamended soil. This was, in part, due to an increase in the soil suspension pH with ISS amendment.     

Heavy metal pollution status in surface sediments of Swan Lake lagoon and Rongcheng Bay in the northern Yellow Sea

The national ‘Shandong Peninsula Blue Economic Zone Development Plan’ compels the further understanding of the distribution and potential risk of metals pollution in the east coast of China, where the rapid economic and urban development have been taken off and metal pollution has become a noticeable problem. Surface sediments collected from the largest swan habitat in Asia, the Swan Lake lagoon and the surrounding coastal area in Rongcheng Bay in northern Yellow Sea, were analyzed for the total metal concentrations and chemical phase partitioning of five heavy metals (Cu, Zn, Pb, Cd, and Cr). Metal contents in the studied region have increased significantly in the past decade. The speciation analyzed by the sequential extraction showed that Zn and Cr were present dominantly in the residual fraction and thus of low bioavailability, while Cd, Pb and Cu were found mostly in the non-residual fraction thus of high potential availability, indicating significant anthropogenic sources. Among the five metals, Cd is the most outstanding pollutant and presents high risk, and half of the surface sediments in the studied region had a 21% probability of toxicity based on the mean Effect Range-Median Quotient. At some stations with comparable total metal contents, remarkably different non-residual fraction portions were determined, pointing out that site-specific risk assessment integrating speciation is crucial for better management practices of coastal sediments.     

Phosphorus fractionation and bio-availability in Taihu Lake(China) sediments

Introduction Sediment phosphorus has been recognized as the mostcritical nutrient limiting lake productivity (OECD, 1982).The concentration of phosphorus in the sediment is often1000 fold higher than that in lake water and its release…     

高原喀斯特土壤有机碳短期稳定的温度作用机制

探明有机碳稳定的温度作用机制,是评估全球变化背景下土壤碳源/汇演变趋势的关键.应用土壤密度分组和酸水解技术,采用红外线辐射增温法,对比研究不同升温情景下高原喀斯特土壤及其物理和生化组分中有机碳密度的短期(4a)变化特征.升温情景包括不升温(对照)、对称升温(全年同步升温2.0℃)和非对称升温(冬春/夏秋季升温幅度为2.5℃/1.5℃、3.0℃/1.0℃、3.5℃/0.5℃和4.0℃/0℃,低度、中度、高度和极端非对称升温),其中中度非对称升温与该区域多年升温情景类似.结果表明,不同升温情景下表层(0~15 cm)土壤有机碳密度在1.95~2.02 kg·m-2之间,其差异不显著,且与对照(1.94 kg·m-2)差异不显著.升温处理间土壤轻组和重组碳密度、重组顽固性碳密度差异不显著,且与对照差异不显著.5个升温处理轻组顽固性碳平均密度是对照的1.18倍,其中对称升温、低度和中度非对称升温处理显著高于对照.轻组顽固性碳密度和轻组顽固性碳指数随升温的非对称性增加而降低,其中对称升温处理均显著高于中度、高度和极端非对称升温.亚表层(15~30 cm)土壤及其物理和生化组分中有机碳密度对短期升温均不敏感.研究揭示:短期内,升温提高了高原喀斯特土壤非保护组分中有机碳顽固性.基于对称升温情景并不一定会误估全球变暖对土壤有机碳数量和土壤碳物理保护能力的影响,但可能会高估表层土壤(0~15 cm)非保护组分有机碳顽固性.     

城市污水处理厂进水氨氧化菌对活性污泥系统的季节性影响

为考察进水氨氧化菌(AOB)对活性污泥系统的季节性影响,对未设置初沉池的西安市第二污水处理厂中进水及活性污泥的氨氧化活性及群落结构进行长期调查分析.结果 表明,进水及活性污泥的比氨氧化速率(SAUR)分别为0.48 ～ 3.02 mg· (g·h)-1和0.68～2.25 mg·(g·h)-1,相关性分析结果显示进水S...