垃圾焚烧飞灰处理处置研究进展

针对作为危险废物的垃圾焚烧飞灰,介绍了近年来国内外对其进行处理处置的研究情况.飞灰的固化/稳定化处理主要从水泥(沥青)固化、熔融固化及化学药剂固化几方面进行论述,飞灰中重金属的提取主要从酸碱浸提、生物浸提、螯合剂浸提及电渗析法提取几方面进行论述.     

基于B/S+C/S的矿山安全标准化管理信息系统研究

首先介绍了安全标准化实施的关键步骤、技术特点及其在矿山的应用,通过现场调研、安全培训,危害辨识与风险评价、文件汇编等环节在山西某矿山建立了安全标准化管理信息系统,在此基础上开发了与之相配套的、基于B/S和C/S混合模式的、在局域网上运行的应用软件--矿山安全标准化管理信息系统.系统由统一信息发布平台、即时报警系统、安全记录管理系统、统计分析系统等14个子系统组成.系统的应用提升了矿山安全生产整体水平,实现了矿山安全标准化和信息化.     

基于GSM的远程家庭智能监控系统设计

针对现有的GSM无线网络,介绍了基于GSM的远程家庭智能报警系统的设计及实现方法.利用各种传感器对家中可能出现的各种意外情况进行采集,并通过PT2262/PT2272组建的家中内部无线网络及时向单片机进行中断报警.GSM模块在单片机控制下,利用GSM网络,将各种报警信息通过短信的方式发送到预先设定的手机中,达到了远程无线智能报警的功能.经过测试,该系统经济、可靠、稳定性高.家庭无需为传感器布线,具有广泛的市场推广价值.     

基于网络的智能视频监控系统的设计与实现

基于网络的智能视频监控就是将自动视频分析技术应用到网络视频监控系统中.提出了一种由分析单元、中心服务器和客户端3个部分组成的智能视频监控系统架构方案.通过对定标、DirectShow、TCP/RTP以及Xvid等关键技术在智能视频监控系统的3个组成部分中的作用来说明系统的设计方案,同时指出了实现自动视频分析的各种关键技术和方法.实验结果表明,该解决方案具有良好的可重用性和扩展性.     

WTO“稀土案”与中国自然资源出口管制的完善

举世瞩目的 WTO"稀土案"于2014年8月7日终落帷幕。同先前的"原料案"一样,中国还是难逃败诉的命运。上诉机构支持申诉方的大部分指控,再次否决了《1994年关税与贸易总协定》(General Agreement on Tariffs and Trade of 1994,以下简称GATT)第20条对中国《入世议定书》的可适用性,从而确认中国对稀土、钨、钼三种原材料采取的出口税及配额等管制措施违背了WTO相关规则和入世所作的特殊承诺。作为自然资源的进出口大国,在自然资源贸易纠纷(特别是出口管制问题)不断"升温"和WTO争端解决机制运用愈来愈频繁的今天,中国应认真总结和反思这场"稀土保卫战"失利带来的经验教训,以从源头上破解中国出口管制措施在WTO体制下遭遇的法律困境,避免今后类似案件败诉的重现。基于此,本文综合应用案例分析、文本分析、历史分析和比较分析等方法对"稀土案"争讼的焦点和争端解决机构(DSB)的裁决意见做了详尽的透析,结果发现此案中DSB的审理不同程度存在着解释僵化、无视中国缔约真意及主观随意、前后矛盾等失范之处,对中国颇为不公。不过,该案也从另外一方面暴露出中国出口管制立法的疏漏与实施缺陷。是故,本文建议中国:1请求部长级会议/总理事会对GATT与《入世议定书》关系做出统一解释,并单独将出口税承诺纳入减让表;2重视DSB既有的裁决思路,根据WTO规则修改相关出口管制法规;3加强资源开采的法律管控,提高资源税的征收标准;4确保对内外资源需求企业的管制一致,优化出口许可管理,努力从WTO法和国内法两个层面推动现行自然资源出口秩序的完善,使中国今后对自然资源的出口管制既能符合WTO规则又能达致确保本国经济可持续性发展之目的。     

基于卫星夜间灯光数据的中国分省碳排放时空模拟

中国能源统计数据"横向不可比,纵向不可加"现象依然突出,尤其是分省能源消费统计千差万别,给分省碳排放评估带来了较大困难,如何利用卫星遥感数据科学合理地估算中国分省碳排放是当前亟须研究的问题。本文运用DMSP/OLS全球稳定夜间灯光数据,在通过相互校正、年内融合和年际间校正等系列处理得到中国分省稳定夜间灯光数据的基础上,首先分别构建中国分省稳定夜间灯光亮度DN值与人均碳排放和单位面积碳排放之间的时空地理加权回归模型,两个模型整体效果均较好,拟合优度分别高达96.74%和99.24%;其次运用稳定夜间灯光亮度DN值对分省人均碳排放和单位面积碳排放进行时空模拟;最后运用人口规模和土地面积对分省碳排放进行估算。估算结果显示:(1)整体来看,2000—2013年年均碳排放模拟值与实际值6.3349×109t较为接近,两个模型的相对误差均在0.5%以内。(2)分年度来看,所有年份的相对误差均在5%以内,2006年分省加总碳排放模拟值与实际碳排放6.2036×109t最为接近,绝对误差和相对误差均较小,两个模型模拟值的相对误差均为0.04%。(3)分省域来看,2000—2013年年均碳排放模拟值与实际碳排放均非常接近,除海南和宁夏外,其余28个省区市的相对误差均在1%以内。(4)分年度分省域来看,以2013年为例,40%省份的相对误差在2%以内,70%省份的相对误差在5%以内。从整体、分年度、分省域、分年度分省域的估算结果来看,基于稳定夜间灯光数据的中国分省碳排放时空模拟效果良好。因此,运用卫星夜间灯光数据可以较为准确地对中国分省碳排放进行估算和预测,为卫星遥感影像数据服务分省碳排放监测和评估提供一种补充性参考。     

Polychlorinated dibenzo-p-dioxins/furans and dioxin-like polychlorinated biphenyls in food and feed in the Lithuanian market

Foods and feeds were analyzed during the period of 2007–2014 employing validated and accredited methods based on gas chromatography–high-resolution mass spectrometry. Sampling has been carried out in-line with national monitoring programs as well as during import controls into Lithuania. Food samples such as eggs, milk, beef, pork, poultry, fats of plant and animal origin, fish, cod liver, and feed samples such as premixes, feeds of plant origin, compound feed, mineral feed, vegetable oil, and fish meals were analyzed. Most of the samples exhibited concentrations below maximum limits, except cod liver. Health impacts were assessed in respect to human daily intakes. Data between groups are compared.     

The conversion of chicken manure to biooil by fast pyrolysis I. Analyses of chicken manure,biooils and char by 13C and 1H NMR and FTIR spectrophotometry

Fast pyrolysis of chicken manure produced two biooils (Fractions I and II) and a residual char. All four materials were analyzed by chemical methods, ¹³C and 1H Nuclear Magnetic Resonance Spectrometry (¹³C and 1H NMR), and Fourier Transform Infrared Spectrosphotometry (FTIR). The char showed the highest C content and the highest aromaticity. Of the two biooils Fraction II was higher in C, yield and calorific value but lower in N than Fraction I. The S and ash content of the two biooil fractions were low. The Cross Polarization Magic Angle Spinning (CP-MAS) ¹³C NMR spectrum of the initial chicken manure showed it to be rich in cellulose, which was a major component of sawdust used as bedding material. Nuclear Magnetic Resonance (NMR) spectra of the two biooils indicated that Fraction I was less aromatic than Fraction II. Among the aromatics in the two biooils, we were able to tentatively identify N-heterocyclics like indoles, pyridines, and pyrazines. FTIR spectra were generally in agreement with the NMR data. FTIR spectra of both biooils showed the presence of both primary and secondary amides and primary amines as well as N-heterocyclics such as pyridines, quinolines, and pyrimidines. The FTIR spectrum of the char resembled that of the initial chicken manure except that the concentration of carbohydrates was lower.     

Effect of UV radiation and temperature on mineralization and volatilization of coumaphos in water

This study was undertaken to determine the dissipation and degradation of coumaphos [O-(3-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl) O,O-diethyl phosphorothioate] under different sunlight conditions and at different temperatures. The effect of the ultra violet (UV) component of solar radiation was also studied using quartz tubes in addition to other radiation in the visible range using glass tubes and the results were compared with those obtained under the dark light conditions. Water suspensions of coumaphos were incubated at three temperatures viz. 22°C, 37°C and 53°C in closed systems to study the effect of temperature. Volatilization, mineralization and degradation of coumaphos increased with an increase in temperature and exposure to solar radiation, particularly under the UV component of the solar radiation. Major loss of the pesticide occurred through volatilization. The optimum temperature for the degradation of coumaphos was found to be at 37°C. The data obtained from the mineralization and degradation studies indicated that 53°C crosses the biological range for suitable growth of microorganism. UV radiation exposure along with maintaining temperature at 37°C may prove useful in the dissipation and/or degradation of coumaphos prior to its disposal as waste from cattle dipping vats.     

Evaluation and validation of two different chromatographic methods (HPLC and LC-MS/MS) for the determination and confirmation of ochratoxin A in pig tissues

This study was undertaken to compare two different analytical methods for the determination and confirmation of ochratoxin A (OTA) in blood serum, kidney and liver of pigs. Sample clean-up was based on liquid-liquid phase extraction. The detection of OTA was accomplished with high-performance liquid chromatography (HPLC) combined either with fluorescence detection (FL) or electro spray ionization (ESI+) tandem mass spectrometry (MS–MS). Comparative method evaluation was based on the investigation of 90 samples of blood serum, kidney and liver per animal originating from different regions of Serbia. The analytical results are discussed in view of the respective method validation data and the corresponding experimental protocols. In general, analytical data obtained with (LC–MS–MS) liquid chromatography electro spray tandem mass spectro metry detection offered comparable good results at the sub-ppb concentration level. The results indicate that the liquid chromatography electro spray tandem mass spectrometric (LC-MS/MS) method was more specific and sensitive for the analysis and confirmation of ochratoxin A in pig tissues then high pressure liquid chromatography (HPLC) method after methylation of OTA.