玉米干旱等级划分及气象产量评估方法

分别以(玉米年雨量平均值±0.5倍标准差)和(平均值±1.5倍标准差)界定不同等级的干旱年份,分析了干旱年对玉米产量的影响,通过对玉米生育期气象条件的分析,建立了玉米气象产量评估方程。     

基于RS/GIS和RUSLE的福建武步溪流域土壤侵蚀研究

将地理信息系统(GIS)、遥感技术(RS)和美国修正的通用土壤流失方程(RUSLE)相结合对武步溪流域的土壤侵蚀量进行计算.运用ERDASIMAGINE 8.4软件对武步溪流域2001年和2003年的遥感影像进行监督分类,结合数字高程模型(DEM)和土壤分布图在ArcView3.2软件平台上获取RUSLE模型中的LS、C、P、R因子,通过ArcView3.2软件进行数据处理和叠加分析,最终得到武步溪流域两个年份的土壤侵蚀等级的空间分布图及土壤侵蚀量.研究结果表明:2001年和2003年中度侵蚀及其以上等级的土壤侵蚀量分别占同年总侵蚀量的88.1%和59.8%,2001年的土壤侵蚀状况比2003年更为严重,其主要原因是2001年降雨侵蚀因子大于2003年的降雨侵蚀因子.改变不合理的土地利用方式将有利于改善该流域土壤流失状况.     

脱水污泥等温干燥特性实验研究及回归分析

利用热重差热分析仪（DTG）对脱水污泥进行干燥实验,测定干燥参数和干燥条件对脱水污泥等温干燥特性的影响,研究了3个温度水平（85℃,100℃,120℃）,5个空气流速（10mL/min,20mL/min,40mL/min,50mL/min,70mL/min）和3个升温速率（15℃/min,20℃/min,40℃/min）。结果表明,样品的干燥速率随着终温的升高、升温速率和空气流速的增大而加快。脱水污泥的干燥过程主要分为加速、恒速和降速3个阶段,且降速干燥段在整个干燥过程中所占的比例较大。其干燥数学模型符合Page方程,经拟合得到 。验证表明,拟合方程算得的MR值与实验结果比较接近。该模型方程可用于描述城市污水污泥的干燥。     

从璧山之痛到“治污典范”——重庆璧南河治污攻坚战

14条受污染的次级河流肯定能治好,璧南河就是最好的例子!2010年9月29日,在全市主城区次级河流综合整治现场工作会上,璧南河污染治理经验被作为次级河流治污典范向全市推广。璧南河,璧山境内最大的次级河流,璧山的母亲河,主河道全长73千米,流域面积441平方千米,涉及璧山境内9个镇街,县域70%以上的经济总量分布在沿河流域。水黑如墨,臭不可闻,鱼虾绝迹曾经是其真实的写照,老百姓怨声载道。按照     

Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous silicates hybrid materials

Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water. A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment.     

美国氮氧化物排放交易经验及启示

综述了美国氮氧化物排放交易项目的演进过程,总结其实践经验,并探讨美国经验对中国氮氧化物排放控制的借鉴意义。     

《环境工程》投稿指南

<正>一、征稿内容1.工业、厂矿和民用领域产生的废气、废水、固体废弃物等的防治和综合利用新技术。2.污染防治创新性改进的工艺、设备、方法、材料以及运行管理经验。3.各行业节能减排和清洁生产技术。4.受污染场地的修复技术。5.环境质量、污染物监测技术和环境评价领域的创新技术和经验。二、稿件具体要求     

Removal of phosphate from wastewater using alkaline residue

Alkaline residue(AR) was found to be an efficient adsorbent for phosphate removal from wastewater. The kinetic and equilibrium of phosphate removal were investigated to evaluate the performance of modified alkaline residue. After treatment by NaOH(AR-NaOH), removal performance was significantly improved, while removal performance was almost completely lost after treatment by HCl(AR-HCl). The kinetics of the removal process by all adsorbents was well characterized by the pseudo second-order model. The Langmuir model exhibited the best correlation for AR-HCl, while AR was effectively described by Freundlich model. Both models were well fitted to AR-NaOH. The maximum adsorption capacities calculated from Langmuir equation were in following manner: AR-NaOH AR AR-HCl. Phosphate removal by alkaline residue was pH dependent process. Mechanisms for phosphate removal mainly involved adsorption and precipitation, varied with equilibrium pH of solution. For AR-HCl, the acid equilibrium pH( 6.0) was unfavorable for the formation of Ca-P precipitate, with adsorption as the key mechanism for phosphate removal. In contrast, for AR and ARNaOH, precipitation was the dominant mechanism for phosphate removal, due to the incrase on pH( 8.0) after phosphate removal. The results of both XRD and SEM analysis confirmed CaHPO4·2H2O formation after phosphate removal by AR and AR-NaOH.     

怎样变信息为企业治污压力

污染控制的障碍到底是什么？这不只是一个技术问题或者资金问题．最核心的问题还是缺乏动力。这个动力原本应该源自严格的执法。源自司法介入的环境诉讼,但是我国现在还不具备这些。从国际经验看,环境保护需要广泛的社会参与,除了政府监管,包括立法、司法、环保行政部门的作为．还有市场手段和公众参与。在西方国家,司法手段可以起到非常重要的作用。而我国环境司法系统还需要进一步完善,这会是一个相当艰难和漫长的过程。     

基于车流和大气污染物浓度同步增量的机动车平均排放因子估算方法

机动车尾气排放已成为城市大气污染的主要来源并受到了高度关注.机动车排放因子是反映机动车排放状况的最基本参数,但实测排放因子代价较高、代表范围有限,基于国外排放模式估算的排放因子又与我国的实际排放状况存在一定差距.本研究首先基于早高峰时段车流量和道路附近大气污染物浓度呈近线性增加、气象条件和背景污染物浓度相对稳定的特征,将时段内污染物浓度的增加主要归因为车流的增加,从而建立车流和污染物浓度增量之间的关系;然后采用无限线源高斯扩散模式,反推道路实际行驶机动车的平均排放因子.以北京市一条主干道为例,利用早高峰车流量、污染物浓度、气象观测数据,进行了实例研究,并将研究结果同COPERT4排放模型的预测结果进行了对比.本研究和COPERT4排放模型预测的8月一氧化碳平均排放因子分别为2.0 g·km-1和1.2 g·km-1,12月分别为5.5 g·km-1和5.2 g·km-1.结果表明,本方法估算的机动车排放因子在数值大小及季节变化上均与COPERT4排放模型较为接近.所提方法通过消除背景浓度的干扰,为实时获取车队实际排放因子提供了一种新思路.