A complete set of procedure for determination of multiresidue of pesticides in vegetables

A complete set of procedure for determination of multiresidue of pesticides in vegetables was presented in this paper.The complete set of procedure included three steps:bioassay,cholinesterase inhibition and GLC analysis.The samples could be identified to be contaminated with pesticides if 5% of house flies was knocked down in 50 tested house flies. Those samples contaminated with pesticides needed to be detected by AChE inhibition method.The qualitative and quantitative analyses were carried out by GLC.Recoveries ranged from 83.7% in Chinese cabbages to 105.6% in tomatoes for pyrethroids,and 84.0% in tomatoes to 102.7% in sweetbell redpeppes for organophosphorus compounds.Coefficients of variations ranged from 0.59% to organophosphorus compounds.Coefficients of variations ranged from 0.59% to 7.87% for pyrethroids. and 0.33% to 9.88% for organophosphorus compounds with vegetables. The complete set of procedure has been used successfully to analyze 7000 samples collected in Beijing. About 1% of the samp     

Humic acid and free radical in environment of Kaschin-Beck disease areas

The humic acid contents in drinking water and soil in Kaschin-Beck disease areas were found more than that of non-disease areas in this research. Changes of free radical concentration in drinking water were agreed with that of humic acid contents in drinking water of Kaschin-Beck disease areas. A positive correlation of free radical concentration and humic acid content in drinking water has been shown (r=0.913) . The structure of I. R. spectra of humic acid under ultraviolet light has been changed. Thus it indicated that free radical was resulted from benzoqiunonyl groups of humic acid in environment.     

Resourcefulization approaches to pollution control of chromate residues in China

Over 2 million tons of chromate residues as hazardous wastes have been accumulated from chromate production processes during the past more than 30 years in China. Some serious pollution problems have been caused due to no appropriate technology and management. Approaches are reviewed to pollution control of chromate residues by utilizing them as secondary resources in this paper. In addition to legislation for pollution control, chromate residues can be used as raw materials to produce a great diversity of useful industrial products. Strategies are also recommanded for the resourcefulization of chromate residues.     

三门火山盆地的层状矿床及其与盆地形成演化的关系

浙江三门中生代火山——沉积盆地的形成演化可分四个阶段。每一阶段均伴产有不同成因和各具特色的金属矿床,显示了陆相火山作用较为完整的成矿体系。其中层状矿床具有同生和后生的双重特征,多成因,多来源,是较典型的火山沉积——后期热液迭加改造型矿床。本文着重介绍它的主要特征及盆地的形成演化对火山成因矿床的控制。     

环境资源约束下中国工业绿色全要素水资源效率研究

通过构建RAM-SFA-RAM三阶段工业绿色全要素水资源效率测度模型，对其不同层面的效率值进行多维测度与比较分析，并利用空间Tobit模型对工业绿色全要素水资源效率的驱动机制进行实证检验.效率测度结果表明，环境因素与统计噪音是效率值计算中不可忽视的重要影响因素；全国样本的效率值在2000~2017年期间总体变化趋势是以持续上升为主，但距离理想发展状态还存在较大差距，具体阶段上可划分为“稳增期”、“振落期”和“提速期”；区域层面的检验中，东部效率具有较为显著的领先优势，而中部和东北部效率差异性相对较小，其变化曲线存在明显的“交互性”现象，西部则整体效率偏低；主要经济带的检验中，京津冀地区的工业绿色全要素水资源效率整体上要高于泛珠三角和泛长三角地区.驱动机制检验表明，基于全国样本维度的水资源禀赋、企业技术创新、用水结构和环境规制对工业绿色全要素水资源效率具有正向促进作用，而产业结构、城镇化率表现为负向抑制效应；在区域样本检验中，各影响要素在不同区域之间所呈现出的作用效果存在一定差异性，但产业结构调整、城镇化水平等应引起重视，不同区域需要依据其实际特点采取针对性的改进措施.     

环境与人口、经济和科技发展的协同探析

本文从环境与人口、经济和科技之间的相依关系出发，探讨了诸因素相互关联的内在协同机理，简析了IPAT模型的建构与应用。嗣后，利用IPAT模型解析了中国近15年来人口、经济和科技发展对环境影响的贡献差异；指出经济规模的迅速扩展和落后技术支持下的传统生产方式是加剧环境恶化的元凶，且技术转型期的负面影响也是不可忽视的重要因素；进而提出了中国未来环境与人口、经济和科技协同演化的对策措施。     

颗粒活性炭对UASB处理垃圾渗滤液促进作用的研究

通过对比研究,考查了用UASB处理垃圾渗滤液时,投加颗粒活性炭对加速UASB反应器中污泥颗粒化进程、缩短启动时间、提高处理效果的影响。结果显示:启动时间缩短了近1/3,最大有机负荷提高近40%且出现了更大颗粒污泥,但COD去除效率没有明显提高。     

分光光度法测定嘉陵江中总磷

采用美国HACH公司DR/5000紫外可见分光光度计,及其专用试剂测定嘉陵江(南充段)上游、下游水样中总磷含量.测定总磷含量(以PO3-4计)适用范围(0.06 mg/L～3.50 mg/L),精密度和灵敏度较好,准确度高,标准物质的回收率都近于100%.对于样品中存在的干扰因素进行了有效的消除.简化了实验操作过程,使测试方法更加简便、快捷、试剂用量少,该方法通过美国环保局(USEPA)认可.     

Comparison of Black Carbon,Total Organic Carbon,and PAH Concentrations in Surface Sediments from Two Main Rivers in Henan Province,China

Black carbon (BC) in surface sediments from Henan section of Yellow River and Huaihe River, China, was determined. Average content of BC in Huaihe River was 0.33%, higher than that in Yellow River (n?=?23) with mean value of 0.15%. Distribution patterns of BC in Yellow River and Huaihe River were similar, namely that tributaries had higher BC content than main stream. In addition, BC content in the mainstream of Yellow River and Huaihe River decreased with altitude. The BC content presented a significant positive correlation with clay (r?=?0.672; p?<?0.01) content in Yellow River, while neither did in Huaihe River. The ratio of BC/TOC ranged from 1.8–57.4% (median 29.6%), evidencing pyrogenic fossil fuel source of BC in Yellow River. Relatively low values of BC/TOC in Huaihe River (5.3%–28.8%, median 7.5%,) reflected that the origin of BC is from burning of biomass. In addition, Pearson rank correlation analysis showed that BC was in strong correlation with lighter PAH in Yellow River, while BC was in significant correlation with heavier PAH in Huaihe River. The ratio of BC/TOC indicated that BC in Yellow River mainly came from fossil fuel combustion, while BC in Huaihe River was primarily from biomass burning.     

Separation and capture of CO2 from large stationary sources and sequestration in geological formations--coalbeds and deep saline aquifers

The topic of global warming as a result of increased atmospheric CO2 concentration is arguably the most important environmental issue that the world faces today. It is a global problem that will need to be solved on a global level. The link between anthropogenic emissions of CO2 with increased atmospheric CO2 levels and, in turn, with increased global temperatures has been well established and accepted by the world. International organizations such as the United Nations Framework Convention on Climate Change (UNFCCC) and the Intergovernmental Panel on Climate Change (IPCC) have been formed to address this issue. Three options are being explored to stabilize atmospheric levels of greenhouse gases (GHGs) and global temperatures without severely and negatively impacting standard of living: (1) increasing energy efficiency, (2) switching to less carbon-intensive sources of energy, and (3) carbon sequestration. To be successful, all three options must be used in concert. The third option is the subject of this review. Specifically, this review will cover the capture and geologic sequestration of CO2 generated from large point sources, namely fossil-fuel-fired power gasification plants. Sequestration of CO2 in geological formations is necessary to meet the President's Global Climate Change Initiative target of an 18% reduction in GHG intensity by 2012. Further, the best strategy to stabilize the atmospheric concentration of CO2 results from a multifaceted approach where sequestration of CO2 into geological formations is combined with increased efficiency in electric power generation and utilization, increased conservation, increased use of lower carbon-intensity fuels, and increased use of nuclear energy and renewables. This review covers the separation and capture of CO2 from both flue gas and fuel gas using wet scrubbing technologies, dry regenerable sorbents, membranes, cryogenics, pressure and temperature swing adsorption, and other advanced concepts. Existing commercial CO2 capture facilities at electric power-generating stations based on the use of monoethanolamine are described, as is the Rectisol process used by Dakota Gasification to separate and capture CO2 from a coal gasifier. Two technologies for storage of the captured CO2 are reviewed--sequestration in deep unmineable coalbeds with concomitant recovery of CH4 and sequestration in deep saline aquifers. Key issues for both of these techniques include estimating the potential storage capacity, the storage integrity, and the physical and chemical processes that are initiated by injecting CO2 underground. Recent studies using computer modeling as well as laboratory and field experimentation are presented here. In addition, several projects have been initiated in which CO2 is injected into a deep coal seam or saline aquifer. The current status of several such projects is discussed. Included is a commercial-scale project in which a million tons of CO2 are injected annually into an aquifer under the North Sea in Norway. The review makes the case that this can all be accomplished safely with off-the-shelf technologies. However, substantial research and development must be performed to reduce the cost, decrease the risks, and increase the safety of sequestration technologies. This review also includes discussion of possible problems related to deep injection of CO2. There are safety concerns that need to be addressed because of the possibilities of leakage to the surface and induced seismic activity. These issues are presented along with a case study of a similar incident in the past. It is clear that monitoring and verification of storage will be a crucial part of all geological sequestration practices so that such problems may be avoided. Available techniques include direct measurement of CO2 and CH4 surface soil fluxes, the use of chemical tracers, and underground 4-D seismic monitoring. Ten new hypotheses were formulated to describe what happens when CO2 is pumped into a coal seam. These hypotheses provide significant insight into the fundamental chemical, physical, and thermodynamic phenomena that occur during coal seam sequestration of CO2.