Effective EU and Member State policies for stimulating CCS

Although CO₂ capture and storage (CCS) is widely recognised as an option to mitigate climate change, consistent and effective EU policies to advance CCS are still absent. This paper discusses policy instruments for advancing large-scale deployment of CCS in the European Union, and evaluates them in a multi-criteria analysis. The EU Emissions Trading Scheme (EU-ETS) is a cost-effective instrument for limiting greenhouse gas emissions, but it is questionable whether its currently limited time horizon and short-trading periods will lead to substantial CCS diffusion. Complementary policies at the EU and the Member State level may repair this and provide sufficient incentives for CCS. Potential policies include financial instruments such as investment subsidies, a feed-in scheme, or a CO₂ price guarantee, as well as a CCS mandate or a low-carbon portfolio. These policy options differ with respect to their environmental effectiveness, possible interaction with the EU-ETS, costs and financial risk involved, and their competition with other mitigation options. Interactions between Member State policies and the EU-ETS are smaller in scope than those of EU-wide policies, but they are more likely to lead to displacement of financial resources from other low-carbon technologies. In addition, national policies may pose a significant part of the financial risk of CCS operations with Member States, reducing the operator's incentive to innovate. Overall, structural policies at the EU level, such as a mandate or a low-carbon portfolio standard would be more conducive for realising large-scale deployment of CCS across the EU as well as more acceptable to environmental organisations.     

Assessing the economic feasibility of regional deep saline aquifer CO2 injection and storage: A geomechanics-based workflow applied to the Rose Run sandstone in Eastern Ohio, USA

Typical top-down regional assessments of CO₂ storage feasibility are sufficient for determining the maximum volumetric capacity of deep saline aquifers. However, they do not reflect the regional economic feasibility of storage. This is controlled, in part, by the number and type of injection wells that are necessary to achieve regional CO₂ storage goals. In contrast, the geomechanics-based assessment workflow that we present in this paper follows a bottom-up approach for evaluating regional deep saline aquifer CO₂ storage feasibility. The CO₂ storage capacity of an aquifer is a function of its porous volume as well as its CO₂ injectivity. For a saline aquifer to be considered feasible in this assessment it must be able to store a specified amount of CO₂ at a reasonable cost per ton of CO₂. The proposed assessment workflow has seven steps that include (1) defining the storage project and goals, (2) characterizing the geology and developing a geomechanical model of the aquifer, (3) constructing 3D aquifer models, (4) simulating CO₂ injection, (5,6) evaluating CO₂ injection and storage feasibility (with and without injection well stimulation), and (7) determining whether it is economically feasible to proceed with the storage project. The workflow was applied to a case study of the Rose Run sandstone aquifer in the Eastern Ohio River Valley, USA. We found that it is feasible in this region to inject 113 Mt CO₂/year for 30 years at an associated well cost of less than US $1.31/t CO₂, but only if injectivity enhancement techniques such as hydraulic fracturing and injection induced micro-seismicity are implemented.     

Decomposition of paper wastes in presence of ceramics and cement raw material

Paper recycling is an environmental important activity that is carried out in all the countries, but during the recycling process a paper waste is produced. Generally these wastes are placed in landfill sites but it is possible to profit it as secondary fuel and raw material in manufacture furnaces.

In this work the combustion of the waste papers with cement and ceramic raw material has been studied with the objective to analyse the interaction of these substances with the emitted pollutants like PAHs and PCDD/Fs.

The results of the study show that the presence of inorganic material produces an increment in the lighter PAH emission but chlorinated compounds are not affected. The PCDD/F emission level found in the combustion of this waste is quite low compared with other wastes subjected to similar conditions.     

Mixing-controlled biodegradation in a toluene plume--results from two-dimensional laboratory experiments

Various abiotic and biotic processes such as sorption, dilution, and degradation are known to affect the fate of organic contaminants, such as petroleum hydrocarbons in saturated porous media. Reactive transport modeling of such plumes indicates that the biodegradation of organic pollutants is, in many cases, controlled by mixing and therefore occurs locally at the plume's fringes, where electron donors and electron-acceptors mix. Herein, we aim to test whether this hypothesis can be verified by experimental results obtained from aerobic and anaerobic degradation experiments in two-dimensional sediment microcosms. Toluene was selected as a model compound for oxidizable contaminants. The two-dimensional microcosm was filled with quartz sand and operated under controlled flow conditions simulating a contaminant plume in otherwise uncontaminated groundwater. Aerobic degradation of toluene by Pseudomonas putida mt-2 reduced a continuous 8.7 mg L(-1) toluene concentration by 35% over a transport distance of 78 cm in 15.5 h. In comparison, under similar conditions Aromatoleum aromaticum strain EbN1 degraded 98% of the toluene infiltrated using nitrate (68.5+/-6.2 mg L(-1)) as electron acceptor. A major part of the biodegradation activity was located at the plume fringes and the slope of the electron-acceptor gradient was steeper during periods of active biodegradation. The distribution of toluene and the significant overlap of nitrate at the plume's fringe indicate that biokinetic and/or microscale transport processes may constitute additional limiting factors. Experimental data is corroborated with results from a reactive transport model using double Monod kinetics. The outcome of the study shows that in order to simulate degradation in contaminant plumes, detailed data sets are required to test the applicability of models. These will have to deal with the incorporation of existing parameters coding for substrate conversion kinetics and microbial growth.     

基于混沌、灰色理论模型,预测煤矿生产中安全状况的对比分析

建立煤矿安全生产状况预测的非线性回归模型、混沌动力学模型、灰色模型和灰色残差模型,用4种模型对我国百万吨煤矿死亡率进行预测分析,其结果表明:混沌动力学预测模型和非线性回归模型使用参数较少、计算简单,易于推广,但预测精度尚不高,误差较大;使用灰色残差模型进行预测,虽然计算复杂,但预测精度较高,验证2007年度百万吨死亡率相对误差仅为0.96%,煤炭生产的安全性指标百万吨死亡率宜采用残差模型进行预测。笔者认为,灰色残差模型在对煤矿安全生产的宏观管理领域有广泛的应用前景。     

橡胶促进剂M盐废水生物处理技术研究

为探讨微生物技术在橡胶促进剂M盐废水处理中的应用,利用高效优势蘸强化A2O工艺对橡胶促进剂M盐废水进行处理,整个系统运行过程分为污泥的培养与驯化阶段及稳定运行阶段。在稳定运行阶段COD0平均去除率达90．71％,氨氮平均去除率达78．31％。以Mn^2＋、Fe^2＋、Mg^2＋、Ni^2＋为4个影响因子,通过正交实验分析无机离子对橡胶促进剂M盐废水中有机物降解的促进作用。由实验数据的摄差大小可知,各无机离子对优势复合菌降解橡胶有机废水的影响从大到小依次为：Mn^2＋、Fe^2＋、Ni^2＋和Mg^2＋。4种离子最佳质量浓度组合为：0．500mg／L的Mn^2＋、1．00mg／L的Fe^2＋、35．0mg／L的Mg^2＋和0．025mg／L的Ni^2＋。     

啤酒酵母吸附Cu^2＋的模拟实验

研究了啤酒酵母吸附重金属Ｃｕ２＋离子的可行性及反应条件对去除作用的影响．结果表明：用啤酒酵母处理Ｃｕ２＋,在起始浓度ρ０为２０～４００ｍｇ／Ｌ的范围内,吸附量ｗ为２．９８～１２．０３ｍｇ／ｇ,说明用啤酒酵母去除重金属Ｃｕ２＋是可行的．吸附反应在１０～２０ｍｉｎ基本达到吸附平衡．最适反应温度（θ）和ｐＨ分别为１５～２０℃和４．０～６．０,酵母细胞有一最适投加用量．Ｆｒｅｕｎｄｌｉｃｈ吸附等温方程的分析表明,η与重金属离子种类有关,与酵母细胞种类关系较小;ｋ值与酵母种类和重金属离子种类有关．     

蔬菜作物施用耐氨固氮菌的增产效果

研究在小区试验条件下,施用耐氨固氮型的催娩克氏菌和阴沟肠杆菌混合菌剂对蔬菜生长和产量的影响。结果表明,施用耐氨固氮菌可促进蔬菜生长,提高产量并改善品质,供试蔬菜的平均增产率达20％,增产效果明显。     

上海地区农业气象灾害监测警示系统的研究

上海地区农业气象灾害监不系统是以实时气象数据为基础,根据农业气象灾害指标进行了评判分析,反映了农业气象灾害,接着,基于Activex的Web/GIS平台展示灾害的分布,并通过Internet网络,提供了多用户服务。     

固相微萃取-气相色谱/质谱联用法测定饮用水中苯类化合物

用固相微苹取(ＳＰＭＥ)－气相色谱/质谱联用法测定饮用水中苯类化合物,以１００μｍ ＰＤＭＳ(聚二甲基硅氧烷)萃取针提取、浓缩、分离与测定九种目标化合物．萃取时间经优化选定为８ｍｉｎ,而热解析时间设定为２ｍｉｎ． 本方法的相对标准偏差小于５%,线性范围宽(２０ｎｇ·ｍｌ－１－１００００ｎｇ·ｍｌ－１),多数化合物的检测限低于５μｇ·ｌ－１．饮用水样品检测显示,样品加标回收率范围在８４%至１１０%内．