黑道凶日研究

本文提出的优势期和优势值是灾害年内出现机会最多的日期和强度，其中优势期就是黑道凶日。统计表明，黑道凶日位于节气日和节气之间的黄金分割日及其附近，在时空分布上具有许多特点。     

Low-reactive circulating fluidized bed combustion (CFBC) fly ashes as source material for geopolymer synthesis

In this contribution, low-reactive circulating fluidized bed combustion (CFBC) fly ashes (CFAs) have firstly been utilized as a source material for geopolymer synthesis. An alkali fusion process was employed to promote the dissolution of Si and Al species from the CFAs, and thus to enhance the reactivity of the ashes. A high-reactive metakaolin (MK) was also used to consume the excess alkali needed for the fusion. Reactivities of the CFAs and MK were examined by a series of dissolution tests in sodium hydroxide solutions. Geopolymer samples were prepared by alkali activation of the source materials using a sodium silicate solution as the activator. The synthesized products were characterized by mechanical testing, scanning electron microscopy (SEM), X-ray diffractography (XRD), as well as Fourier transform infrared spectroscopy (FTIR). The results of this study indicate that, via enhancing the reactivity by alkali fusion and balancing the Na/Al ratio by additional aluminosilicate source, low-reactive CFAs could also be recycled as an alternative source material for geopolymer production.     

Co-metabolic transformation of the neonicotinoid insecticide imidacloprid by the new soil isolate Pseudoxanthomonas indica CGMCC 6648

A new imidacloprid (IMI) degrading bacterium Z-9 (deposited number CGMCC 6648) was isolated and identified as Pseudoxanthomonas indica by 16S rRNA gene analysis. Two metabolites were identified as olefin and 5-hydroxy IMI by liquid chromatography-mass spectrometry and nuclear magnetic resonance analysis. P. indica CGMCC 6648 degraded 70.1% of IMI (1.22 mmol L^?1) and formed 0.93 mmol L^?1 5-hydroxy IMI and 0.05 mmol L^?1 olefin IMI in 6 days and in the presence of 100 mmol L^?1 glucose. The half-life of IMI degradation was 3.6 days. P. indica CGMCC 6648 transforms IMI via a co-metabolism mechanism and different carbohydrates have significant effects on 5-hydroxy IMI formation, whereas different organic acids have substantial effects on olefin IMI production. Lactose is the best co-substrate for IMI degradation and 5-hydroxy IMI formation with 0.77 mmol L^?1 degraded and 0.67 mmol L^?1 formed in 48 h, respectively. Pyruvate is the best co-substrate for olefin IMI formation with 0.17 mmol L^?1 produced in 96 h for all carbon sources tested. Pyruvate significantly stimulates the conversion of 5-hydroxy IMI to olefin IMI, whereas glucose slightly inhibits this reaction. P. indica CGMCC 6648 rapidly degrades IMI and forms olefin IMI, which may enhance its potential for biodegradation of IMI and increase its insecticidal activity, which can decrease the IMI dosage required.     

PRB技术修复铬污染地下水的试验研究

以铬污染地下水为研究对象,用零价铁作为反应介质设计了可渗透反应墙(PRB),对零价铁处理铬污染地下水的处理效果和长期稳定性进行了研究。对不同粒径的铁粉处理效果进行对比,发现铁粉粒径越小,处理效果越好。用铁粉作为PRB反应介质,对PRB处理铬污染地下水的长期稳定性进行了研究。试验结果表明,采用Fe0-PRB原位技术处理铬污染地下水,铁粉粒径越小处理废水的水质越好,但介质粒径越小,反应器渗透系数越小,处理水量显著减少;且铁粉在处理含铬废水时生成了大量的难溶化合物,容易造成填料堵塞,导致铁粉利用效率不高。因此有必要研制铁粉复合填料,增大填料的渗透性,提高填料处理含铬废水时铁粉的利用效率。     

关于燃煤电厂环境影响评价工作中的一些问题

对燃煤电厂的环评工作中，项目选址、总平面布置、污染防治与清洁生产：冷却塔噪声等一些值得注意的问题进行了探讨，并提出了一些初步意见。     

天然气应用对兰州大气环境的影响

煤烟型污染是兰州市大气污染严重的主要原因之一，西气东输工程对改变兰州市能源结构，改善城市环境质量具有非常重要的意义。根据兰州市大气污染现状和特性，以2000年为基准，分析研究了兰州市利用天然气前后能源结构，主要污染源及大气污染物排放量的变化。针对污染源状况和兰州市天然气用气规划，选用适宜模式预测了兰州市利用天然气后的各主要污染物的年平均浓度，计算了空气质量的改善程度。     

应用植物酯酶抑制技术测定蔬菜水果中农药残留量

应用植物酯酶的抑制技术,测定蔬菜水果中有机磷和氨基甲酸酯类农药残留量的简易薄层—植物酶抑制(TLC-EI)法。该法对多种农药的最小检出量为毫微克(ng)级,最小检出浓度为0.01pm,添加回收率在80％以上。     

Spatial PM2.5 mobile source impacts using a calibrated indicator method

Motor vehicles are major sources of fine particulate matter (PM_2.5), and the PM_2.5 from mobile vehicles is associated with adverse health effects. Traditional methods for estimating source impacts that employ receptor models are limited by the availability of observational data. To better estimate temporally and spatially resolved mobile source impacts on PM_2.5, we developed an approach based on a method that uses elemental carbon (EC), carbon monoxide (CO), and nitrogen oxide (NO_x) measurements as an indicator of mobile source impacts. We extended the original integrated mobile source indicator (IMSI) method in three aspects. First, we generated spatially resolved indicators using 24-hr average concentrations of EC, CO, and NO_x estimated at 4 km resolution by applying a method developed to fuse chemical transport model (Community Multiscale Air Quality Model [CMAQ]) simulations and observations. Second, we used spatially resolved emissions instead of county-level emissions in the IMSI formulation. Third, we spatially calibrated the unitless indicators to annually-averaged mobile source impacts estimated by the receptor model Chemical Mass Balance (CMB). Daily total mobile source impacts on PM_2.5, as well as separate gasoline and diesel vehicle impacts, were estimated at 12 km resolution from 2002 to 2008 and 4 km resolution from 2008 to 2010 for Georgia. The total mobile and separate vehicle source impacts compared well with daily CMB results, with high temporal correlation (e.g., R ranges from 0.59 to 0.88 for total mobile sources with 4 km resolution at nine locations). The total mobile source impacts had higher correlation and lower error than the separate gasoline and diesel sources when compared with observation-based CMB estimates. Overall, the enhanced approach provides spatially resolved mobile source impacts that are similar to observation-based estimates and can be used to improve assessment of health effects.

Implications: An approach is developed based on an integrated mobile source indicator method to estimate spatiotemporal PM_2.5 mobile source impacts. The approach employs three air pollutant concentration fields that are readily simulated at 4 and 12 km resolutions, and is calibrated using PM_2.5 source apportionment modeling results to generate daily mobile source impacts in the state of Georgia. The estimated source impacts can be used in investigations of traffic pollution and health.     

氧化-混凝法处理碱性高砷废水的实验研究

对碱性高砷废水的处理进行了研究 ,针对常规混凝法除砷的缺点提出了氧化 混凝工艺。结果表明 ,用氧化 混凝工艺除砷效果显著 ,废水经处理后砷含量低于 0 5mg/L ,符合国家排放标准。氧化 混凝除砷的最佳工艺条件为 :pH值为 6— 7,H2 O2 用量为 2 5 % ,氧化时间为 10min ,Fe2 (SO4) 3 用量为 2 5g/L ,PAM用量为 11 2 5mg/L。