中国北方气候变化对小麦产量的影响——基于EPIC模型的模拟研究

中国的粮食产量在过去的几十年中一直保持着稳定的增长，农业技术在其中起到了重要的作用。但随着全球气候变暖及其导致的气候极端事件的增加，气候变化对作物生长和产量造成了不同的影响。选用美国农业部提出的EPIC（Environmental Policy Integrated Climate）农作物生长模型评价了气候变化对小麦产量的影响。基于EPIC模型，模拟了中国北方80个典型站点的春小麦和冬小麦1961—2005年期间的生长过程，分析了不同作物类型、不同灌溉类型和不同农业区域小麦产量的波动，以及生长季辐射、水分胁迫因子和温度胁迫因子对产量波动的影响。结果表明：在不考虑农业技术因素的条件下，辐射的波动是导致小麦产量波动的主要原因；温度胁迫的降低在一定程度上促进了小麦的增产。     

Industrial metabolism of chlorine: a case study of a chlor-alkali industrial chain

Substance flow analysis (SFA) is applied to a case study of chlorine metabolism in a chlor-alkali industrial chain. A chain-level SFA model is constructed, and eight indices are proposed to analyze and evaluate the metabolic status of elemental chlorine. The primary objectives of this study are to identify low-efficiency links in production processes and to find ways to improve the operational performance of the industrial chain. Five-year in-depth data collection and analysis revealed that system production efficiency and source efficiency continued increasing since 2008, i.e., when the chain was first formed, at average annual growth rates of 21.01 % and 1.01 %, respectively. In 2011, 64.15 % of the total chlorine input was transformed into final products. That is, as high as 98.50 % of the chlorine inputs were utilized when other by-products were counted. Chlorine loss occurred mostly in the form of chloride ions in wastewater, and the system loss rate was 0.54 %. The metabolic efficiency of chlorine in this case was high, and the chain system had minimal impact on the environment. However, from the perspectives of processing depth and economic output, the case study of a chlor-alkali industrial chain still requires expansion.     

废印制线路板真空热解产物分析

在自行设计的间歇式固定床真空热解装置中热解废印制线路板(PCB),对热解产物进行了分析.在热解温度为550 ℃、热解压力为20 kPa、恒温时间为60 min的条件下,得到的热解产物质量分数为:热解渣70%;热解油3%～4%;不可冷凝热解气26%～27%.经气相色谱-质谱联用(GC-MS)分析,热解油经常压蒸馏后得到的低沸点液态油中含有29种化合物,主要有苯酚、对异丙基酚、3-乙基酚、4-甲酚及2-溴苯酚,还含有少量含溴化合物和含氯化合物.热解油经简单的蒸馏就可达到回收酚类化合物的目的.热解渣经风选可实现铜与黏附有碳黑的玻璃纤维的分离,其中铜质量分数约30%,黏附有碳黑的玻璃纤维质量分数约70%.     

Traffic and meteorological impacts on near-road air quality: summary of methods and trends from the Raleigh Near-Road Study

A growing number of epidemiological studies conducted worldwide suggest an increase in the occurrence of adverse health effects in populations living, working, or going to school near major roadways. A study was designed to assess traffic emissions impacts on air quality and particle toxicity near a heavily traveled highway. In an attempt to describe the complex mixture of pollutants and atmospheric transport mechanisms affecting pollutant dispersion in this near-highway environment, several real-time and time-integrated sampling devices measured air quality concentrations at multiple distances and heights from the road. Pollutants analyzed included U.S. Environmental Protection Agency (EPA)-regulated gases, particulate matter (coarse, fine, and ultrafine), and air toxics. Pollutant measurements were synchronized with real-time traffic and meteorological monitoring devices to provide continuous and integrated assessments of the variation of near-road air pollutant concentrations and particle toxicity with changing traffic and environmental conditions, as well as distance from the road. Measurement results demonstrated the temporal and spatial impact of traffic emissions on near-road air quality. The distribution of mobile source emitted gas and particulate pollutants under all wind and traffic conditions indicated a higher proportion of elevated concentrations near the road, suggesting elevated exposures for populations spending significant amounts of time in this microenvironment. Diurnal variations in pollutant concentrations also demonstrated the impact of traffic activity and meteorology on near-road air quality. Time-resolved measurements of multiple pollutants demonstrated that traffic emissions produced a complex mixture of criteria and air toxic pollutants in this microenvironment. These results provide a foundation for future assessments of these data to identify the relationship of traffic activity and meteorology on air quality concentrations and population exposures.     

构建新农村防震减灾规划体系的初步探讨

本文从地震灾害的破坏概况入手,结合当前新农村防震减灾规划存在的问题,揭示了新农村防震减灾规划体系要点,以供读者把握我国新农村规划建设的整体印象,在新农村规划中具有一定的理论价值和实际指导意义。     

混凝-活性炭-膜工艺处理黄磷化工渗滤液的研究

采用混凝-活性炭-膜工艺对黄磷化工渗滤液进行处理,重点考察了该工艺对有机物的去除机制.实验结果表明,混凝剂硫酸铝的投加量为0.2g/L时,渗滤液中各污染物去除率较好;颗粒活性炭对渗滤液中有机物的吸附容量几乎不受渗滤液pH的影响,吸附等温线更符合修正的Freundlich模型,拟二级动力学模型能更好地定量描述有机物在颗粒活性炭上的吸附过程;膜处理进一步提高了剩余有机物和其他污染物的去除率.     

Cu-SBA-15催化湿式过氧化氢氧化水溶液中罗丹明B

采用水热晶化法合成了不同含铜量的Cu—SBA-15介孔分子筛，并且用XRD、N2吸附、TEM以及uV—vis对所合成的样品进行表征。以Cu—SBA-15为催化剂，H2O2为氧化剂，催化湿式过氧化水溶液中的罗丹明B，主要考察H2O2浓度、催化剂用量、处理温度、初始pH等因素对罗丹明B氧化效果的影响。结果表明，在同样的处理条件下罗丹明的脱色率明显高于TOC去除率，处理温度、初始pH对罗丹明B的脱色与氧化有重要影响。在罗丹明B初始浓度100mg／L，H2O2初始浓度1．8g／L，催化剂量0．3g／L，温度60℃，pH为7．0，处理时间100min时，罗丹明B的脱色率为98．6％，TOC去除率为62．8％。     

气溶胶中有机物的研究进展和前景

首先指出了气溶胶中有机物的研究意义 ,接着介绍了目前对气溶胶中有机物的化学组成、来源和成因、环境和健康效应的认识 ,综述了分析测试方法的研究现状 ,并评述了其研究前景     

中国煤炭消费对PM2.5污染的影响研究

国务院颁布的《大气污染防治行动计划》明确提出制定国家煤炭消费总量中长期控制目标,到2017年,煤炭占能源消费总量比重降低到65%以下,然而煤炭消费对PM_(2.5)污染的贡献到底多大,这是当前亟待研究的科学问题。为定量分析煤炭消费对我国PM_(2.5)污染的影响,本研究首先计算了2012年煤炭消费产生的大气污染物排量,然后利用CAMx空气质量模型,分别采用组分分析法和情景模拟法两种方法研究了煤炭消费对全国PM_(2.5)污染的影响。组分分析法研究表明,煤炭消费对全国PM_(2.5)年均浓度的贡献率约为61%,其中煤炭直接燃烧、煤炭相关行业的贡献率分别约为37%、24%;情景模拟法研究表明,煤炭消费对全国PM_(2.5)年均浓度的贡献率约为56%。因此,我国由于煤炭消费对全国PM_(2.5)年均浓度的贡献率为56%~61%。     

Spatial Extent of Sediment Toxicity in U.S. Estuaries and Marine Bays

Acute, laboratory toxicity tests were performed by the National Oceanic and Atmospheric Administration (NOAA) on 1543 surficial sediment samples collected during 1991 through 1997 throughout 25 estuaries and marine bays. Selected areas were sampled along the Atlantic, Gulf of Mexico, and Pacific coasts. The toxicity of each sample was determined with 10-day amphipod survival tests performed with solid-phase (bulk) sediments. Collectively, the 1543 samples tested through 1997 represented a total area of approximately 7300 km². Toxicity was observed with the amphipod survival tests in samples that represented approximately 6% of the combined area. Using similar tests conducted on samples collected in different, but overlapping, study areas, the U.S. Environmental Protection Agency (EPA) estimated that approximately 7% of the combined estuarine area sampled was toxic. Generally, toxicity was most severe in northeastern and southwestern estuaries and least prevalent in southeastern and northwestern areas. However, considerable portions of the Pacific coast have not been tested with the same methods. In tests of CYP1A enzyme induction (n=464), samples were toxic that represented about 5% of the combined study areas. Toxicity was much more widespread, however, when the results of two sub-lethal tests were analyzed. Significant results occurred in samples that represented approximately 25% and 39% of the study areas in tests of sea urchin fertilization (n=1309) and microbial bioluminescence (n=1215), respectively.