户用沼气模式生命周期减排清单与环境效益分析

相对于传统农业活动,以沼气为纽带的生态农业生产具有清洁的能源生产和高度闭环的废物回收处置等明显优势,在全国范围内得到入户推广。本文综合考虑沼气工程建造、使用和综合利用等生命周期过程,分析了典型户用沼气池综合利用各阶段环境节能减排清单,并在此基础上评价其环境效益。结果表明,"猪-沼-稻-果"综合农业利用模式下单位沼气池节能减排效果明显,其中CO2、PM10、CH4和CO净减排量分别达3 060.700kg、19.820kg、12.960kg和75.590kg,总净节能达9 068.4MJ。其中,玉米秸秆、沼液沼渣的利用和燃煤替代对温室效应的减缓明显,畜禽粪便的利用和燃煤的替代减缓了环境酸化以及富营养化过程,而光化学氧化的减缓主要来自玉米秸秆的利用而减少的CO、VOC的排放,沼气工程对人体毒害的减缓主要是来自燃煤替代而减少的SO2和PM10排放。户用沼气利用对各种环境影响均有减缓作用,其中对光化学氧化、富营养化、环境酸化和温室效应的改善最为显著,对于降低能源耗竭、减缓对人体的毒性也起到了较好的作用。     

Trace metal occurrence and distribution in sediments and mangroves,Pumicestone region,southeast Queensland,Australia

The Pumicestone region is a unique catchment in northern Moreton Bay, southeast Queensland. The region supports a wide range of land-use activities as well as attractions such as nature conservation areas. One environmental aspect that has not previously been addressed in this area is the occurrence of minor and trace metals in estuarine sediments associated with the main estuaries of the region. The trace metals included in this investigation are: vanadium, chromium, molybdenum, cobalt, nickel, copper, zinc, cadmium, lead and arsenic. To determine and evaluate the occurrence and distribution of metals in the area, several components have been analysed: bedrock material, pre-industrial settings, recent estuarine sediments, soils of estuarine origin and mangrove pneumatophores. The 40 sites chosen for sediment and soil samples cover a variety of estuarine settings and represent a range of natural conditions in terms of channel and bank morphology, tidal energy, vegetation cover, relationship to bedrock, water salinity and land disturbance. The chemical, mineralogical and statistical analyses employed in this study enabled (a) establishment of background values for the area, (b) determination of relationships between metals and (c) identification of sites with anomalous metal concentrations. All the metals found in the sediments of the area are sourced from the geological bedrock. The dominant trace elements identified in sediments are Zn, V and Cr. The remaining metals are highly variable spatially. All trace metals are controlled by the presence of Fe and Mn oxides, and by the grainsize of the sediment. Typically, fine-grained Fe-rich materials tend to adsorb more trace metals than sandy sediments. In soils that have developed from estuarine muds, some metals such as Cr, Mo, Pb and As tend to be in larger quantities than in the estuarine counterparts. Some of the elements, which occur in significant amounts in the sediment, have been detected in mangrove tissue (Avicenniamarina) such as V, Cr, Zn, Fe and Mn. Of particular note is Cu, which is present in mangrove tissue in quantities many times exceeding the sediment concentration. The comparative analysis of pre-industrial settings and recent sediments and soils highlighted some areas of metal enrichment such as acid-affected sites where oxidation of pyrite has mobilised metals from sediments; these metals are then redistributed in Fe-rich surficial layers. Disturbed banks within the estuaries are also likely to have low levels of metal enrichment due to boating activities.     

Absorbed dose delivered by alpha particles calculated in cylindrical geometry

The present work aims to develop a semi-analytical method to calculate the absorbed dose delivered by alpha particles in a cylindrical geometry. This method will be employed to reproduce the dose conversion coefficients or absorbed fraction of alpha particles in sensitive cells of the tracheobronchial tree obtained by NRC and ICRP, respectively. The difference caused by using water stopping power and tissue stopping power will also be investigated. Linear stopping powers for alpha particles in tissue and air were calculated, and the dependences of stopping powers on the traveled distance were established. A geometry model is set up for our calculations, and two different cases have been considered, namely the near-wall and far-wall cases. The total energy imparted to a unit-diameter sphere around a point is shown to be obtainable from a triple integral, which can be solved numerically. The absorbed dose is found to be independent of the diameter of the sphere being considered and additional assumptions about its diameter were not needed. The results obtained are in good agreement with those obtained previously by NRC and ICRP66. Using the semi-analytical method developed in the present work, the dose conversion coefficients or absorbed fraction previously obtained by NRC and ICRP, respectively, have been satisfactorily reproduced. Using the tissue stopping power instead of the water stopping power can slightly lower the values for dose conversion coefficients in the bronchial region.     

An assessment of the toxicity of pyridinium chlorides and their biodegradation intermediates

Toxicity investigations were conducted for four pyridinium chlorides belonging to cationic surface-active substances (CSAS), which differed from each other in the numbers of methyl groups (CH(3)) in pyridinium ring.The crustacean Daphnia magna, the fish Lebistes reticulatus and the alga Scenedesmus quadricauda were chosen as biotests. Toxicity of examined preparations appeared to be very high but did not depend on their chemical structure. S. quadricauda was the most sensitive organism. Toxicity of intermediate products obtained in biological oxidation process was also examined. Biodegradation was conducted according to the "river water test". It was found that only partial degradation took place while pyridinium chlorides constituted main energy and carbon source. Presence of biodegradation intermediate products was shown on the basis of 1H NMR analysis. Intermediates were not toxic to any biotests.     

Volatile organic compounds in indoor environment and photocatalytic oxidation: state of the art

Volatile organic compounds (VOCs) are the major pollutants in indoor air, which significantly impact indoor air quality and thus influencing human health. A long-term exposure to VOCs will be detrimental to human health causing sick building syndrome (SBS). Photocatalytic oxidation of VOCs is a cost-effective technology for VOCs removal compared with adsorption, biofiltration, or thermal catalysis. In this paper, we review the current exposure level of VOCs in various indoor environment and state of the art technology for photocatalytic oxidation of VOCs from indoor air. The concentrations and emission rates of commonly occurring VOCs in indoor air are presented. The effective catalyst systems, under UV and visible light, are discussed and the kinetics of photocatalytic oxidation is also presented.     

Remediation of water pollution caused by pharmaceutical residues based on electrochemical separation and degradation technologies: A review

In the last years, the decontamination and disinfection of waters by means of direct or integrated electrochemical processes are being considered as a very appealing alternative due to the significant improvement of the electrode materials and the coupling with low-cost renewable energy sources. Many electrochemical technologies are currently available for the remediation of waters contaminated by refractory organic pollutants such as pharmaceutical micropollutants, whose presence in the environment has become a matter of major concern. Recent reviews have focused on the removal of pharmaceutical residues upon the application of other important methods like ozonation and advanced oxidation processes. Here, we present an overview on the electrochemical methods devised for the treatment of pharmaceutical residues from both, synthetic solutions and real pharmaceutical wastewaters. Electrochemical separation technologies such as membrane technologies, electrocoagulation and internal micro-electrolysis, which only isolate the pollutants from water, are firstly introduced. The fundamentals and experimental set-ups involved in technologies that allow the degradation of pharmaceuticals, like anodic oxidation, electro-oxidation with active chlorine, electro-Fenton, photoelectro-Fenton and photoelectrocatalysis among others, are further discussed. Progress on the promising solar photoelectro-Fenton process devised and further developed in our laboratory is especially highlighted and documented. The abatement of total organic carbon or reduction of chemical oxygen demand from contaminated waters allows the comparison between the different methods and materials. The routes for the degradation of the some pharmaceuticals are also presented.     

X-ray absorption spectroscopy studies of reactions of technetium, uranium and neptunium with mackinawite

Technetium, uranium and neptunium may all occur in the environment in more than one oxidation state (IV or VII, IV or VI and IV or V respectively). The surface of mackinawite, the first-formed iron sulfide phase in anoxic conditions, can promote redox changes so a series of laboratory experiments were carried out to explore the interactions of Tc, U and Np with this mineral. The products of reaction were characterised using X-ray absorption spectroscopy. Technetium, added as TcO4(-), is reduced to oxidation state IV and forms a TcS(2)-like species. On oxidation of the mackinawite in air to form goethite, Tc remains in oxidation state IV but in an oxide, rather than a sulfide environment. At low concentrations, uranium forms uranyl surface complexes on oxidised regions of the mackinawite surface but at higher concentrations, the uranium promotes surface oxidation and forms a mixed oxidation state oxide phase. Neptunium is reduced to oxidation IV and forms a surface complex with surface sulfide ions. The remainder of the Np coordination sphere is filled with water molecules or hydroxide ions.     

Measurement and modeling of oxidation rate of hydrogen isotopic gases by soil

Measurements of oxidation rate of hydrogen isotopic gases by soil were made to model HT oxidation rate by soil. Soil was sampled at a cultivated farmland and laboratory measurements of the oxidation rate of H(2) and D(2) gases simulating HT gas were carried out under controlled conditions of soil. The oxidation rate increased with increase of H(2) or D(2) concentration in air and nearly saturated at high concentration. The oxidation rate was low under extremely dry and wet soil conditions and was the highest at soil water content of 8-14 w/w%. The oxidation rate increased exponentially with increasing soil temperature and was the highest at 46 degrees C. Michaelis constant K(m) increased exponentially with increasing soil temperature. Oxidation rate of H(2) was generally higher than that of D(2), while K(m) of H(2) was generally lower than that of D(2). From these results, oxidation rate of HT was modeled as a product of the functions that represent dependency on each soil factor.     

Potential use of solar energy for waste activated sludge treatment

The use of solar energy as a disintegration unit operation for waste activated sludge was tested in a pilot plant. The effect of the treatment process on chemical oxygen demand (COD), total suspended solids (TSS), settling time and filtration index was investigated in single (solar) and sequential processes (solar & biological). Solar oxidation was found to be a good sludge disintegration technology. Available solar photons were utilised to degrade the soluble organic matter and release the cell liquids. The highest COD and TSS removal efficiencies were obtained by the month of June. Sequential process efficiencies were related to accumulate solar photons, aerobic treatment time and operational condition. Sequential process resulted in COD and TSS removal efficiency of 16% and 13%, respectively. Increasing aerobic treatment time and/or mixing the oxidised sludge with fresh sludge improved COD and TSS removal efficiencies to 23% and 27%, respectively. The use of sequential processes improves the settling tendency of sludge by bio-oxidation of the released portions and eliminates protein charge effect on sludge settling.     

Recent advances in the bioremediation of arsenic-contaminated groundwater

The biological treatment of groundwater is used primarily to remove electron donors from water sources, providing (biologically) stable drinking water, which preclude bacterial regrowth during subsequent water distribution. To the electron donors belong also the dissolved metal cations of ferrous iron and manganese, which are common contaminants found in most (anaerobic) groundwater. The removal of iron and manganese is usually accomplished by the application of chemical oxidation and filtration. However, biological oxidation has recently gained increased importance and application due to the existence of certain advantages, over the conventional physicochemical treatment. The oxidation of iron and manganese is accelerated by the presence of certain indigenous bacteria, the so-called "iron and manganese oxidizing bacteria." In the present paper, selected long-term experimental results will be presented, regarding the bioremediation of natural groundwater, containing elevated concentrations of iron and arsenic. Arsenic is considered as a primary pollutant in drinking water due to its high toxicity. Therefore, its efficient removal from natural waters intended for drinking water is considered of great importance. The application of biological processes for the oxidation and removal of dissolved iron was found to be an efficient treatment technique for the simultaneous removal of arsenic, from initial concentrations between 60 and 80 microg/l to residual (effluent) arsenic concentrations lower than the limit of 10 microg/l. The paper was focused on the removal of As(III) as the most common species in anaerobic groundwater and generally is removed less efficiently than the oxidized form of As(V). To obtain information for the mechanism of As(III) removal, X-ray photoelectron spectroscopy (XPS) analyses were applied and it was found that As(III) was partially oxidized to As(V), which enabled the high arsenic removal efficiency over a treatment period of 10 months.     

Profile of Methane Concentrations in Soil and Atmosphere in Alpine Steppe Ecosystem on Tibetan Plateau

The methane concentration profile from -1.5m depth in soil to 32m height in air was measured in alpine steppe located in the permafrost area. Methane concentrations showed widely variations both in air and in soil during the study period. The mean concentrations in atmosphere were all higher than those in soil, and the highest methane concentration was found in air at the height of 16m with the lowest concentration occurring at the depth of 1.5m in soil. The variations of atmospheric methane concentrations did not show any clear pattern both temporally and spatially, although they exhibited a more steadystable state than those in soil. During the seasonal variations, the methane concentrations at different depths in soil were significantly correlated （R^2〉0.6） with each other comparing to the weak correlations （R^2〈0.2） between the atmospheric concentra- tions at different heights. Mean methane concentrations in soil significantly decreased with depth. This was the compositive influence of the decreasing production rates and the increasing methane oxidation rates, which was caused by the descent soil moisture with depth. Although the methane concentrations at all depths varied widely during the growing season, they showed very distinct temporal variations in the non-growing season. It was indicated from the literatures that methane oxidation rates were positively correlated with soil temperature. The higher methane concentrations in soil during the winter were determined by the lower methane oxidation rates with decreasing soil temperatures, whereas methane production rates had no reaction to the lower temperature. Relations between methane contribution and other environmental factors were not discussed in this paper for lacking of data, which impulse us to carry out further and more detailed studies in this unique area.     

分布式能量系统在我国未来20年能源发展战略中的地位

为了使分布式能量系统（Distributed Energy System,简称DES）在我国更好地发展，本文从我国未来20年的能源发展战略出发，介绍了我国能源发展中依然存在的矛盾和问题，并通过对分布式能量系统组成、特点的研究，认为目前正是分布式能量系统发展的良好机遇：通过对分布式能量系统利用方式的研究，指出了分布式能量系统将在我国未来20年能源发展战略中的地位以及需要解决的相关问题。     

中国建筑业能源效率省际差异及其影响因素分析

我国建筑业存在着高消耗、高污染和低能效等问题。提高建筑业能源效率、降低能源消耗对实现社会经济的可持续发展具有重要意义。本文以中国区域建筑业为研究对象,在全要素能源效率的框架下,基于30个省份2005-2008年的面板数据,利用DEA方法对各省的建筑业能源效率进行测度和评价。结果表明:不同省份建筑业能源效率存在较大差异,其中黑龙江、上海和浙江效率最高,各年的效率值均为1,内蒙古和山东的效率最低,各年的效率值均不足0.3。在此基础上,本文从能源消费结构、产业发展程度、产业组织特征、辅助产业发展程度和科技水平5个方面选取10个变量,利用Tobit回归模型,分析了各变量对能源效率的影响。结果表明:能源消费结构、产业发展程度、产业集中度、市场化程度和外商投资等是导致能源效率省际差异的主要因素。本文建议,应通过提高电力等高效能源的消费比重、适度调整产业结构、提高产业集中度、加强外资引进等措施来提高建筑业能源效率。     

Changing energy intensity in China:a decomposition analysis

This study proposed a decomposition method based on the normalized quadratic shadow unit cost function to explore the determinants of the change in energy intensity in China from 1985 to 2010.The decomposition analysis indicates that (1) the improvement in technical efficiency dramatically reduced the energy intensity,whereas technological change played only a minor role,which could be attributed to a rebound effect;(2) the aggregated allocation effect was small because the change in the allocative distortion between capital and energy significantly enhanced energy intensity but was partly offset by the effect stemming from the change in the allocative distortion between capital and energy;and (3) the substitution of energy for labor increased energy intensity,but the aggregated substitution effect significantly reduced energy intensity because the substitution of capital for energy reduced energy intensity to a great extent.These findings were obtained at the national level and varied at die regional level.     

小城镇能源优化配置研究

构建我国能源安全体系面临诸多困境。小城镇能源保障是其最薄弱的环节之一。但小城镇能源保障及其优化配置问题并没有得到政府、学术界应有的重视。通过与城市的比较分析。得出小城镇能源类型和结构特征，指出能源自然禀赋构成小城镇能源类型和结构的“本底”。社会经济发展水平。产业结构变迁主宰小城镇能源类型和结构变迁。在此基础上，提出了小城镇能源优化配置战略目标和导向。根据这一目标和导向，对小城镇能源优化配置的政策措施进行初步探讨。包括编制小城镇能源资源利用规划；加快可再生能源的应用技术研究；建立小城镇能源资源分配、开发、流通的市场机制；保护小城镇能源资源；优化小城镇产业结构。大力推动循环经济；推广分布式能源供给模式，提高小城镇能源供给安全。     

Energy Analysis of Sugarcane Production in Morocco

An energy analysis of sugarcane production in small and large farms was made in Morocco. Total energy expenditures were 64.90 and 47.83 GJ/ha and energy outputs were 100.80 and 85.80 GJ/ha in large and small farms, respectively. The output/input energy ratios were 1.6 and 1.8. The energy intensity lies between 0.7 and 0.8 MJ/kg and is one of the highest among sugarcane producing countries. Irrigation is the most energy consuming operation with about 50% of total energy inputs. Electricity, fertilizers, fuel, and machinery are the main energy inputs. The influence of the different inputs is discussed and practical measures for energy saving and environmental conservation based on energy analysis are discussed.     

基于二次能源省际调配的中国分省CO2排放量计算

节能减排目标任务的制定需要依据科学合理的CO2排放量测算。现有的IPCC提供的CO2排放量计算方法仅考虑一次能源燃料所产生的CO2,未考虑到二次能源省际调配的情况,不能真实反映各省CO2排放情况。本研究提出了考虑二次能源省际调配情况下CO2排放量的计算方法,并以2009年的数据为例,对各省能源消费CO2排放量进行了计算。考虑二次能源省际调配后,传统的能源大省如内蒙古、山西的CO2排放总量下降,东部沿海省份的CO2排放总量上升。中西部地区的CO2排放强度仍显著高于东部地区。中西部地区存在能源利用效率低、能源加工技术设备落后的情况,导致了西部地区的CO2排放强度偏高。建议中央在实施西部大开发"十二五"规划时,应当加强对中西部地区能源加工行业的投资,改善能源加工技术,改良加工设备,提高能源加工效率,降低CO2排放强度。建议由能源调入省向能源调出省份实施补偿。该部分补偿资金用于调出省的能源产业升级改造,以顺利实现节能减排的目标。     

Energy intensity and its determinants in China: an empirical study based on ARDL-VECM approach

The present study aims to better understand the relationship between energy intensity and its determinants including energy price, technological progress, economic structure, and energy mix using the autoregressive distributed lag(ARDL) bounds approach and vector error correction model technique. Based on China's time series over 1985-2014, the ARDL bounds approach yields empirical evidence that confirms the existence of long run relationship between energy price, technological progress, economic structure, energy mix, and energy intensity. The results show that technological progress is an important driver for the declining energy intensity in short and long run. Energy price has not been demonstrated as an important role in decreasing energy intensity in the short run. The high share of coal use in total energy use may be responsible for China's high energy intensity.However, the relative change in economic sectors plays a minor role in energy intensity reduction during the past years. In the long run, technological progress, energy mix and energy prices Granger cause energy intensity, but not vice versa except for the energy mix.     

Energy Embodied in Goods in International Trade of China: Calculation and Policy Implications

In recent years, China’s energy demand and Greenhouse gas (GHG) emissions have grown very fast, quite an amount of which was exported as energy embodied in goods in international trade rather than consumed domestically. Starting from the concept of embodied energy, based on input-output energy analysis approach, in this paper the energy embodied in goods in international trade of China during the period from 2001 to 2006 is calculated. The results show that although China has become a net importer of petroleum since 1993, China is a net exporter of embodied energy due to international trade in goods. In 2002, the total amount of energy embodied in exported goods was about 410 million tce (ton of coal equivalent, hereinafter referred to as "tce"). Eliminating the amount of energy embodied in imported goods of about 170 million tce, the net export of embodied energy was about 240 million tce, accounting for 16% of the aggregate primary energy consumption of that very year in China, and the net export of embodied emissions was about 150 million tons of carbon. With the rapid growth of China’s international trade, assuming no structural input-output changes of among sectors, in 2006 the net export of embodied energy went up to about 630 million tce, an increase of 162 % over 2002. In addition, this paper also analyzes the possible sources of error in calculation, and also discusses the policy implications according to the result of the calculation.     

Emissions from heated indoor dust

Settled indoor dust was collected from a university building, and the fine fraction was heated in the temperature range of 50-250 degrees C. Emissions of compounds were analysed and identified in a system consisting of a thermal desorption unit coupled to a gas chromatograph-mass spectrometer (GC-MS). The heating took place in both an oxidative (air) and an inert (He) atmosphere. The results indicate that oxidation of adsorbed compounds occurred, as well as decomposition of the dust itself. The emission in air started somewhere between 150 and 200 degrees C, with aldehydes and ketones as the main compounds. When heated in the inert atmosphere, semivolatile organic compounds (SVOCs) were emitted at temperatures above 150 degrees C. These compounds were not found in the air system, probably due to oxidation. Based on the obtained results we recommend that the temperature of hot surfaces in indoor environments should be kept below 150 degrees C to avoid oxidation of indoor dust and minimise the emissions.