区域分工与合作视角下区域产业同构问题及优化路径

区域间产业结构的同构与异构取决于在市场调节和宏观调控中生产要素的结构与流动特征,其特征量的相似性导致产业结构的同构,产业同构在一定时空条件下具有合意性。随着区域经济一体化进程的加快,其非合意性愈显突出。区域产业同构优化的本质动力在于生产要素结构及其流动特征量的变化,通过不同层级区域产业规划战略和区域间经济合作实现生产要素的合理组合与流动,以产业集群化之路实现区域产业结构的高级化,使区域产业结构朝着优化、持续方向发展。     

电力行业的节能减排与低碳经济

中国能源结构以煤为主,火电行业是碳排放量的主体,面对低碳经济的发展模式,电力行业势必将成为CO2减排的主力军。目前,火电行业通过"上大压小"政策,实现结构减排;通过提高电力工业的烟气脱硫,实现工程减排;通过扩大清洁能源的比例,减少煤炭消耗总量,实现总量减排。使用清洁能源是实现碳减排的有效途径。指出了电力行业"节能减排"的现状和措施,分析了电力行业在"低碳经济"中所面临的新形势,并对低碳电力技术的研究与运用进行了展望,阐述了通过利用清洁能源促进碳减排的迫切性和必要性。     

Environmental assessment of garden waste management in the Municipality of Aarhus, Denmark

An environmental assessment of six scenarios for handling of garden waste in the Municipality of Aarhus (Denmark) was performed from a life cycle perspective by means of the LCA-model EASEWASTE. In the first (baseline) scenario, the current garden waste management system based on windrow composting was assessed, while in the other five scenarios alternative solutions including incineration and home composting of fractions of the garden waste were evaluated. The environmental profile (normalised to Person Equivalent, PE) of the current garden waste management in Aarhus is in the order of −6 to 8 mPE Mg⁻¹ ww for the non-toxic categories and up to 100 mPE Mg⁻¹ ww for the toxic categories. The potential impacts on non-toxic categories are much smaller than what is found for other fractions of municipal solid waste. Incineration (up to 35% of the garden waste) and home composting (up to 18% of the garden waste) seem from an environmental point of view suitable for diverting waste away from the composting facility in order to increase its capacity. In particular the incineration of woody parts of the garden waste improved the environmental profile of the garden waste management significantly.     

Plant steroid hormones produced under Ni stress are involved in the regulation of metal uptake and oxidative stress in Brassica juncea L

Brassinosteroids (BRs) are involved in the amelioration of various biotic and abiotic stresses. With an aim to explore the role of BRs under heavy metal stress, plants of Brassica juncea L. were grown in pots. The plants were subjected to various concentrations of Nickel metal (0.0, 0.2, 0.4 and 0.6 mM) and harvested on 60th day in order to observe the expression of these hormones. The isolated BRs from the leaves of Brassica plants characterized by GC-MS include 24-Epibrassinolide (24-EBL), Castasterone, Dolicholide and Typhasterole. The effect of isolated 24-EBL was studied on Ni metal uptake and antioxidative defense system in 60 d old plants of Brassica. It was observed that 24-EBL significantly increased the activities of stress ameliorating enzymes and lowered the metal uptake in plants. This is the first report in B. juncea L. plants showing the expression of BRs under metal treatments and effect of the isolated 24-EBL on metal uptake and in oxidative stress management.     

阿坝州大骨节病和扶贫开发决策中AHP方法的应用

大骨节病防治和扶贫开发试点工作涉及阿坝州的经济、社会、生态等各方面，且州内各县、乡、村情况各异，众多具体措施关系复杂。为了提高决策质量，使试点工作取得“优化举措、重点突破”的效果，应用AHP方法建立了定量模型。     

臭氧同时脱硫脱硝技术研究进展

对利用臭氧同时脱硫脱硝技术进行了综述，分析了臭氧对NOx的脱除机理。臭氧同时脱硫脱硝技术具有明显的一体化脱除特性，但臭氧的发生费用却制约了它的应用。介绍了目前国外在工程上应用的低温氧化技术（LOTOX），分析了其脱除效果及优缺点。     

解磷微生物肥料的研究与进展

磷是植物生长必需的矿物质元素之一，在土壤中易被固定降低其有效性，目前，研究和生产含有解磷功能的微生物有机肥料是转化土壤中无效磷、提高磷肥利用率的有效途径之一。叙述了解磷微生物犯料中微生物的种类、生态分布规律和影响高效解磷微生物选育的外部因素，概述了解磷微生物菌肥的应用和研究进展，探讨了解磷微生物肥料的应用价值。为解磷微生物未来的研究重点提出理论依据。．     

腐熟蓝藻与厌氧污泥混合厌氧发酵特性

采用批次小试实验对不同腐熟程度的蓝藻进行厌氧发酵产沼气实验研究。结果表明,新鲜蓝藻在30-35℃时腐熟7 d后,可在35℃的厌氧温度下获得最高的产气速率和246 mL/g COD的产气量,产气潜力为354 mL/g（VS）。厌氧反应15 d后,累计产气量、COD和VFA浓度趋于稳定。淀粉酶和脱氢酶的活性在厌氧反应初期受到抑制,蛋白酶活性和辅酶F420浓度在厌氧系统中逐渐增加,分别在第6天达到27.66μmol/（g VS·min）和第15天达到0.62μmol/g（VS）。15-18d是腐熟蓝藻适宜的中温厌氧发酵时间,少于以新鲜蓝藻为基质的厌氧消化时间。蓝藻腐熟过程促进了厌氧反应,腐熟7 d的蓝藻厌氧系统具有更高的微生物活性和产甲烷能力。     

The effect of alkyl chain length on the degradation of alkylimidazolium- and pyridinium-type ionic liquids in a Fenton-like system

Background, aim, and scope  Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them, the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride. Materials and methods  The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide. All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with the aid of ¹H NMR. Results  Degradation of ionic liquids in this system was quite effective. Increasing the H₂O₂ concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance to degradation was weaker, the shorter the alkyl chain. Discussion  The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Conclusions  The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium chloride when the resistance of imidazolium ionic liquids decreases with increasing H₂O₂ concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Recommendations and perspectives  Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the future structural design as well as tailor the technological process of these chemicals