颗粒化序列间歇式活性污泥反应器工艺处理化粪池污水

在序列间歇式活性污泥反应器(SBR)中成功培养出适应化粪池污水水质的好氧颗粒污泥.并将其应用于化粪池污水的处理.在好氧颗粒污泥培养的第15天左右,SBR中开始出现细小的颗粒,然后微生物在其上繁殖生长使颗粒逐渐增大而成熟;在第24天时,SBR中絮状活性污泥已基本实现了颗粒化.培养出的好氧颗粒污泥对化粪池污水有稳定的处理效果,在进水完全为化粪池污水时,COD、NH_4~+-N、TN的平均去除率分别为77%、61%、47%.但是,由于化粪池污水COD较低,因此无法维持较高的生物量,在后期的稳定运行过程中MLSS始终维持在2 500 mg/L左右.好氧颗粒污泥的同步硝化反硝化作用是其稳定脱氮的保证.     

Organic aerosol characterization by complementary measurements of chemical bonds and molecular fragments

Organic aerosol chemical markers from normalized concentrations of independent measurements of mass fragments (using Aerosol Mass Spectrometry, AMS) are compared to bond-based functional groups (from Fourier Transform Infrared spectroscopy, FTIR) during eight field projects in the western hemisphere. Several field projects show weak correlations between alcohol group fractions and m/z 60 fractions, consistent with the organic hydroxyl groups and the fragmentation of saccharides, but the weakness of the correlations indicate chemical differences among the relationships for ambient aerosols in different regions. Carboxylic acid group fractions and m/z 44 fractions are correlated weakly for three projects, with correlations expected for aerosols dominated by di-acid compounds since their fragmentation is typically dominated by m/z 44. Despite differences for three projects with ratios of m/z 44 to m/z 57 fragments less than 10, five projects showed a linear trend between the project-average m/z 44 to m/z 57 ratio and the ratio of acid and alkane functional groups. While this correlation explains only a fraction of the fragment and bond variability measured, the consistency of this relationship at multiple sites indicates a general agreement with the interpretation of the relative amount of m/z 44 as a carboxylic acid group marker and m/z 57 as an alkane group marker.     

High time-resolved measurements of organic air toxics in different source regimes

High time-resolved (HTR) measurements can provide significant insight into sources and exposures of air pollution. In this study, an automated instrument was developed and deployed to measure hourly concentrations of 18 gas-phase organic air toxics and 6 volatile organic compounds (VOCs) at three sites in and around Pittsburgh, Pennsylvania. The sites represent different source regimes: a site with substantial mobile-source emissions; a residential site adjacent to a heavily industrialized zone; and an urban background site. Despite the close proximity of the sites (less than 13 km apart), the temporal characteristic of outdoor concentrations varied widely. Most of the compounds measured were characterized by short periods of elevated concentrations or plume events, but the duration, magnitude and composition of these events varied from site to site. The HTR data underscored the strong role of emissions from local sources on exposure to most air toxics. Plume events contributed more than 50% of the study average concentrations for all pollutants except chloroform, 1,2-dichloroethane, and carbon tetrachloride. Wind directional dependence of air toxic concentrations revealed that emissions from large industrial facilities affected concentrations at all of the sites. Diurnal patterns and weekend/weekday variations indicated the effects of the mixing layer, point source emissions patterns, and mobile source air toxics (MSATs) on concentrations. Concentrations of many air toxics were temporally correlated, especially MSATs, indicating that they are likely co-emitted. It was also shown that correlations of the HTR data were greater than lower time resolution data (24-h measurements). This difference was most pronounced for the chlorinated pollutants. The stronger correlations in HTR measurements underscore their value for source apportionment studies.     

Effect of typhoon on atmospheric particulates in autumn in central Taiwan

Previous studies have suggested that the ongoing global climate change will likely increase the intensity and frequency of extreme weather, such as typhoons. Since the beginning of global warming, it has become necessary to understand the influence of typhoons on air quality. Rare data, especially particulate measurements data could be used to establish the relationship between the air pollution and typhoons. One of main limiting factors is that most of the previous chemical analyses of particulates used a relatively long sampling time, which could dilute the temporal impact of particulate characteristics and their sources. This work, depending more time-resolved measurements, focus on the characteristics and sources of high particulate matter levels and the influence of typhoons and the Pacific high system. Depending on the measurements, two pollutant groups were clearly identified in this work. The first pollutant group was the emissions from neighboring riverbeds under the strong circulation of the typhoon in the driest season and characterized as high coarse particle concentrations with high mass fraction of Ca²⁺. The second pollutant group was characterized as the formation and transport of secondary particles with prevalent ions of NH₄⁺, NO₃^?, and SO₄^2? and occurred in the sea-land breeze circulation under the influence the Pacific high system.     

铁改性海泡石除锑的影响因素研究

选择廉价海泡石, 用氯化铁对其改性。研究铁改性海泡石对锑的吸附特性。结果表明,氯化铁浓度、吸附时间、初始锑浓度以及温度等因素对锑的吸附影响较大,溶液初始pH影响不明显。在初始锑浓度50 mg/L,pH 6.8,5%氯化铁改性海泡石投加量为2 g/L,吸附90 min, 温度35℃下,吸附量可达21.6 mg/g。海泡石对吸附锑具有缓冲特性,溶液的初始pH值在3.1～10.1范围时,吸附后溶液的最终pH值为8～8.5。IMS吸附锑是放热过程。改性后海泡石比表面积增大,表面羟基数量增加,导致其吸附能力增强。通过XRD谱图并未发现铁晶体的存在。     

ABR反应器的两种快速启动方法对比

ABR反应器的启动是ABR反应器能否高效稳定运行的关键,其影响因素很多。为了更好地实现ABR反应器的启动,提出了通过2种不同启动方法的对比,即1^#反应器采用好氧预挂膜的方法,2^#反应器采用低负荷启动法,得出的结论为,好氧预挂膜启动法的启动时间短,COD去除率高,出水pH稳定,颗粒状污泥生长情况较好,是一种可推广的启动方法。     

脂肪酰基氨基酸对矿物润滑油生物降解性的影响研究

通过生物降解试验研究了N-月桂酰基谷氨酸、N-月桂酰基甘氨酸、N-月桂酰基丙氨酸和N-油酰基甘氨酸4种脂肪酰基氨基酸对HVI 350矿物润滑油生物降解性的影响,采用高倍电子显微镜分析了生物降解过程中微生物数量和形态变化。结果表明,在矿物润滑油中添加少量脂肪酰基氨基酸后,矿物润滑油的生物降解性能明显改善,且生物降解过程中微生物数量增多、形态发生变化,这可能是脂肪酰基氨基酸增加了微生物的营养,且具有表面活性,有利于细胞的吸收,从而促进了矿物润滑油生物降解。     

砒霜生产化工厂危险废物处置工程设计

通过对砒霜生产化工厂原场址废渣及污染场地调查的基础上,进行了处置方案比选及技术经济比较,确定了就地安全填埋的处置方案。根据区域性危险废物集中安全填埋场的设计经验,本工程采用先进的HDPE双层防渗的安全填埋方式,并设置了雨水分流系统、渗滤液收集系统、封场处理和填埋气体导排系统,整个场区布置合理,对周围环境的影响小,投资少,取得了良好的社会效益和环境效益,并对危险废物处理处置工程设计中应注意的问题提出了建议。     

聚合氯化铝铁去除微污染水体中藻类的研究

以聚合氯化铝铁(PAFC)为絮凝剂,H2O2为预氧化剂,用正交实验研究了PAFC处理微污染水体中藻类和降低浊度,得出正交实验中各因素的主次关系及对除藻和除浊度的影响,研究表明,ρPAFC是影响除藻和除浊度的重要因素.在最佳处理条件,即ρPAFC为20 mg/L,ρH2O2为6 mg/L,pH为7,搅拌时间为4 min,能使水体中藻细胞街度从9.4×107 cells/L降至3.16×106 cells/L,除藻率为96.6%,浊度降至0.70 NTU,除浊度率达93.0%.     

垃圾填埋场微生物气溶胶粒径分布研究

为了了解垃圾填埋场微生物气溶胶粒径分布规律,在北京市某垃圾卫生填埋场填埋区、渗滤液处理区、生活区分别选定监测点,利用安德森六级微生物采样器,对填埋场空气微生物进行了系统的定点取样、测定和分析。研究结果表明,空气细菌粒径分布均为第Ⅰ级(>8.2 μm)最高,填埋区空气细菌粒径呈偏态分布,渗滤液处理区、生活区分别在第Ⅳ级和第Ⅲ级出现第2个峰值。携带细菌的可吸入微粒在渗滤液处理区比例最大。空气真菌与放线菌均在第Ⅳ级分布最高,携带真菌和放线菌的可吸入粒子的比例显著大于细菌(P<0.05)。填埋区不同作业时段空气微生物粒径在各级分布比例基本一致。填埋区细菌气溶胶中值直径为5.7 μm,渗滤液处理区为3.7 μm,生活区为5.3 μm,显著大于真菌气溶胶和放线菌气溶胶的中值直径(P<0.05)。