云贵高原湖区湖泊营养物生态分区技术方法研究

提出一种基于主成分分析、聚类分析、判别分析和空间自相关的分区模型,用于对云贵高原湖区湖泊营养物生态分区的研究.首先运用主成分分析方法对众多指标进行了降维综合处理,产生彼此互补相关又能综合反映湖区情况的4个新指标,累计贡献率达到93.69%,具有充分的代表性,构建了云贵高原湖区湖泊营养物生态分区指标体系.在此基础上,根据各区域新指标值,结合聚类模型初步将湖泊流域分为5类,再利用判别分析完成非湖泊流域的类别判别,最后运用空间自相关分析方法,按聚类结果进行全局自相关分析,Moran’sI为0.320,且检验值Z值为68.2,远大于临界值(显著水平1%所对应的临界值2.58),表明聚类结果与空间位置具有显著相关性,之后运用局部自相关对区域各因素的主成分综合得分的空间分布格局进行了量化分析,揭示了零散分类区块在空间地域分布上的关联和差异,根据关联结果完成最终的分区.结果表明,利用此分区模型可以尽量避免人为因素,得到更为客观的分区结果,具有良好的适应性和可行性,可为探索适合我国湖泊营养物生态分区的指标体系和分区技术方法,完成全国湖泊营养物生态分区和科学地制定我国湖泊营养物基准和富营养化控制标准提供技术支持.     

基于我国规范与PIARC标准的公路隧道需风量分析

以某长大高速公路隧道为例,结合我国隧道通风设计规范JTJ026.1-1999与PIARC2007标准(世界道路协会),针对不同行车速度,不同车辆更新情况、不同排放标准组合形式以及是否考虑NOx等情况,对各个不同工况的需风量分别进行计算,并从需风量计算方法、机动车排放量和污染物设计浓度三个方面对隧道需风量差异进行分析。研究结果表明:我国设计规范与PIARC2007存在较大差距,为了适应当前及今后我国交通量及机动车排放特点的发展趋势,我国现行规范应在机动车排放量、污染物设计浓度限值等方面做出必要改进以达到合理确定隧道需风量的目的。     

硫酸系统水平衡分析计算和生产实践

在硫酸系统中,通过水平衡分析计算烟气带入净化工序的SO2体积分数和含水量,确定净化工序的能力,控制干燥塔进口烟气温度,使干吸工序生产出合格产品;通过计算,烟气带入净化工序的水量小于产品带出的水量,制酸净化污水经过污水处理工序处理后返回到净化工序重复使用,实现净化污水零排放,消除对环境的污染.     

钢渣处理技术的环境性能比较

随着钢铁工业的快速发展,大量钢渣弃置堆积,不仅成为环境污染源,而且占用大量的土地。目前钢渣处理技术较多,其中主要的处理方法有冷弃法、热闷法、热泼法、浅盘法、水淬法、风淬法等。本研究采用生命周期评价方法,对主要钢渣处理技术进行评估,定义了生命周期评估边界和清单指标,建立了清单计算模型,得到了不同钢渣处理技术的生命周期清单。为了提高结果的可信性,对模型进行了不确定性分析。结果表明滚筒法和风淬法的环境性能较好,是值得推广的钢渣处理技术。     

四川某中小城镇污水处理厂进水水质统计分析

生活污水水质对处理工艺的选择、设计参数的选取以及稳定运行十分重要。运用SPSS软件,对四川某中小城镇污水处理厂为期一年的进水指标(水量、COD、氨氮、总磷、pH、SS)进行方差和相关性分析。方差分析结果显示进水量、氨氮和SS在月份和季节之间存在显著性差异,而总磷和pH仅在月份之间存在显著差异,COD在季度和月份之间无显著性差异;指标相关性分析表明,进水量和氨氮之间呈负相关,氨氮和总磷、COD和总磷之间呈正相关,且相关性显著。在此分析的基础上对污水处理厂设计、工艺选择及运行管理提出了一些建议。     

Effect of platinum on the photocatalytic degradation of chlorinated organic compound

TiO2 nanoparticles, doped with di erent Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO2, H2PtCl6 6H2O and methanol as the solvents. The physicochemical properties of Pt/TiO2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray di raction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO2 and Pt/TiO2 were evaluated. The average diameter and BET surface area of the TiO2 catalyst particles were 300 nm and 50 m2/g, respectively. The degradation e ciency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation e ciency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO2 process was capable of e ciently decomposing gaseous DCM in air.     

Chemical cleaning of fouled PVC membrane during ultrafiltration of algal-rich water

Cleaning of hollow-fibre polyvinyl chloride (PVC) membrane with di erent chemical reagents after ultrafiltration of algal-rich water was investigated. Among the tested cleaning reagents (NaOH, HCl, EDTA, and NaClO), 100 mg/L NaClO exhibited the best performance (88.4% 1.1%) in removing the irreversible fouling resistance. This might be attributed to the fact that NaClO could eliminate almost all the major foulants such as carbohydrate-like and protein-like materials on the membrane surface, as confirmed by Fourier transform infrared spectroscopy analysis. However, negligible irreversible resistance (1.5% 1.0%) was obtained when the membrane was cleaning by 500 mg/L NaOH for 1.0 hr, although the NaOH solution could also desorb a portion of the major foulants from the fouled PVC membrane. Scanning electronic microscopy and atomic force microscopy analyses demonstrated that 500 mg/L NaOH could change the structure of the residual foulants on the membrane, making them more tightly attached to the membrane surface. This phenomenon might be responsible for the negligible membrane permeability restoration after NaOH cleaning. On the other hand, the microscopic analyses reflected that NaClO could e ectively remove the foulants accumulated on the membrane surface.     

Effect of manufacturing methods of AgCl/Al2O3 catalyst on selective catalytic reduction of NOx

The AgCl/Al2O3 catalyst has potential for use in the selective catalytic reduction (SCR) of NOx. A compound hydrocarbon, following oxygenation is used as a type of reducing agent. In this experiment, the AgCl/Al2O3 catalyst was produced by four different methods, and the differences among their reduction catalysis of NOx were compared. Ethanol was used as a type of reducing agent. X-ray diffraction analysis was performed to study the crystalline structure and scanning electron microscope and transmission electron microscope (TEM) were applied to determine the microindentation. The results indicated that, in the range of 350–400°C, there was no significant difference on the NOx reduction rate; however, there was dispersion at high and low temperature ranges. The size of the AgCl particles was about 20–100 nm.     

Methanotrophic community structure of aged refuse and its capability for methane bio-oxidation

Aged refuse from waste landfills closed for eight years was examined and found to contain rich methanotrophs capable of biooxidation for methane. Specially, community structure and methane oxidation capability of methanotrophs in the aged refuse were studied. The amount of methanotrophs ranged 61.97 103–632.91 103 cells/g (in dry basis) in aged refuse from Shanghai Laogang Landfill. Type I and II methanotrophs were found in the aged refuse in the presence of sterilized sewage sludge and only Type I methanotrophs were detected in the presence of nitrate minimal salt medium (NMS). The clone sequences of the pmoA gene obtained from the aged refuse were similar to the pmoA gene of Methylobacter, Methylocaldum, and Methylocystis, and two clones were distinct with known genera of Type I methanotrophs according to phylogenetic analysis. Aged refuse enriched with NMS was used for methane biological oxidation and over 93% conversions were obtained.     

气候谈判国际阵营变化的经济学分析

气候谈判关乎各国在气候秩序中的权力与义务关系,涉及到各国经济发展的根本利益,已经成为国际政治博弈的新舞台。当前,欧盟与美国正在突破＂共同但有区别的责任＂原则,争夺气候变化谈判中的领导权;发展中国家阵营逐步分化为＂基础四国＂＂小岛屿国家＂＂最贫穷国家＂等。从长期来看,在气候变化问题上,各国有一致的利益,各国际阵营若能表现出更合作的态度——发达国家更负责地转变为低碳生产和生活模式,更慷慨和带有诚意地协助发展中国家减排,发展中国家更深刻地认识到碳排放空间的来之不易和低碳生产生活的迫切性,实现自觉减排——就能帮助遭遇＂囚徒困境＂的世界各国离开个体理性的＂纳什均衡＂,趋向集体理性的＂帕累托最优＂。