新型高效生物反应器类型和应用

近年来高效生物反应器得到不断发展，出现了多种新型生物反应器。从厌氧升流式生物反应器发展的经验和反应器的特点出发，提出了升流式反应器的结构、三相分离器的形式和污泥颗粒化现象等3个新概念是高效新型反应器的基础，进而在广义升流式污泥床反应器概念的基础上，提出具有传质效率高、处理能力强、有机负荷高以及抗冲击负荷能力强等优点的第三代高效生物反应器概念。     

新型高效生物反应器类型和应用

近年来高效生物反应器得到不断发展,出现了多种新型生物反应器.从厌氧升流式生物反应器发展的经验和反应器的特点出发,提出了升流式反应器的结构、三相分离器的形式和污泥颗粒化现象等3个新概念是高效新型反应器的基础,进而在广义升流式污泥床反应器概念的基础上,提出具有传质效率高、处理能力强、有机负荷高以及抗冲击负荷能力强等优点的第三代高效生物反应器概念.     

气提式内循环膜生物反应器试验研究

针对膜生物反应器存在的膜污染和能耗高的问题，结合气提式内循环和一体式膜生物反应器处理废水的工艺特点，提出圆柱形套筒气提式内循环膜生物反应器。试验结果表明，同等曝气强度和曝气方式下，气提式内循环膜生物反应器中氧传质系数（KLa）高于一般膜生物反应器；膜间水流流速是一般膜生物反应器的1.53～2.44倍，提高了膜面的水力冲刷作用，可减缓膜污染；对反应器膜过滤性能的考察，表明气提式内循环膜生物反应器较一般膜生物反应器有更好的膜过滤性能和抗污染能力。反应器中添加内循环，污泥活性有所下降，但对实际废水的去除效果影响不大，污泥活性较为稳定。     

一种新型的生物处理技术—膜生物反应器

膜生物反应器是近年来发展起来的一种新型的处理技术,现就膜生物反应器的应用类型,机理进行阐述,并对膜生物反应器存在问题和应用前景作了说明,指出膜生物反应器将会成为２１世纪的一种重要的污水处理技术。     

厌氧生物反应器的设计,启动和运行控制方法

厌氧生物反应器的设计，启动和运行控制受施工因素的影响。根据作者的使用体会论述了利用实验室工作数据，指导有效地启动和稳定运行厌氧生物反应器的方法，提供了便于操作的工作程序以及厌氧生物反应器设计的基本方法，作者还就常用的厌氧生物反应器的特性，运行要点提出了建议。     

污水处理中膜生物反应器的脱氮途径

就膜生物反应器污水处理中的硝化与反硝化特性进行了总结。分析和评述了各种膜生物反应器脱氮工艺的原理、特点、实现条件和应用现状;重点推介了一些新型脱氮途径在膜生物反应器中的应用。     

树脂-气升式环流生物反应器的脱氮性能

为了提高废水生物处理过程的脱氮性能,设计了树脂-气升式环流生物反应器,通过实验考察了该反应器连续抗氨氮冲击的能力,并验证了反应器中吸附铵离子的强酸阳离子树脂生物再生的可行性,分析了生物再生机理。结果表明,原水中铵离子之外的阳离子的存在是实现树脂生物再生的关键。     

生物活性炭法深度处理纺织废水二级出水中生物活性的研究

采用上流式曝气生物活性炭法处理碱减量印染废水二级生物处理出水，利用TTC-脱氢酶活性（DHA）法监测反应器内DHA生物活性分布。研究发现反应器内生物炭表面附着生物膜活性较高，特别是反应器上部生物碳粒同样具有较高的DHA活性，这与反应器运行一年多能够保持对COD、色度和UV等较高去除率有一定关系。还研究了活性炭吸附、反应器反冲洗对DHA活性的影响。本研究为曝气生物活性炭法有效去除印染碱减量废水中难降解有机物提供了一定的理论依据。     

MBR在污水处理中的应用

膜生物反应器是生物降解与膜分离相互影响、共同作用的过程。综述了膜生物反应器在污水处理中的应用及发展方向。     

中空纤维膜生物反应器处理造纸废水

膜生物反应器是将膜分离技术与生物处理工艺相结合而开发的新型系统,是近年来新发展起来的高效废水处理技术。本实验采用了中空纤维膜组件和活性污泥反应器组成的分置式膜生物反应器,研究其在造纸废水处理中的特性影响因素。     

膜分离技术在油气回收中的应用

简单阐述了油气回收的意义,并对几种常用的油气回收方法进行了介绍,分析其优缺点,重点论述了膜分离技术在油气回收中的应用,以及国内外的进展情况和典型应用实例,最后对膜法油气回收与其它方法作了比较,对膜法回收现阶段的存在问题进行了剖析,并对今后的研究方向提出了建议。研究结果表明,膜法是一种大有前途的油气回收方法。     

Thermal exploitation of wastes with lignite for energy production

The thermal exploitation of wastewood with Greek lignite was investigated by performing tests in a laboratory-scale fluidized bed reactor, a 1-MW(th) semi-industrial circulating fluidized bed combustor, and an industrial boiler. Blends of natural wood, demolition wood, railroad sleepers, medium-density fiberboard residues, and power poles with lignite were used, and the co-combustion efficiency and the effect of wastewood addition on the emitted pollutants were investigated. Carbon monoxide, sulfur dioxide, and oxides of nitrogen emissions were continuously monitored, and, during the industrial-scale tests, the toxic emissions (polychlorinated dibenzodioxins and dibenzofurans and heavy metals) were determined. Ash samples were analyzed for heavy metals in an inductively coupled plasma-atomic emission spectroscopy spectrophotometer. Problems were observed during the preparation of wastewood, because species embedded with different compounds, such as railway sleepers and demolition wood, were not easily treated. All wastewood blends were proven good fuels; co-combustion proceeded smoothly and homogeneous temperature and pressure profiles were obtained. Although some fluctuations were observed, low emissions of gaseous pollutants were obtained for all fuel blends. The metal element emissions (in the flue gases and the solid residues) were lower than the legislative limits. Therefore, wastewood co-combustion with lignite can be realized, provided that the fuel handling and preparation can be practically performed in large-scale installations.     

Identification and level estimation of chlorinated neutral aromatic sulfur compounds and their alkylated derivatives in pulp mill effluents and sediments

Seven effluent samples from a modern pulp mill, in which chlorine and chlorine dioxide bleaching is used, and five sediment samples from the recipient watercourse were investigated for polychlorinated dibenzothiophenes (PCDBTs), polychlorinated thianthrenes (PCTAs), polychlorinated diphenylsulfides (PCDPSs) and for alkylated derivatives of these. Mainly di-, tri-, tetra- and pentachlorinated congeners were studied. Particles and filtrates from the effluents were analyzed separately. The concentration levels of the nonalkylated compounds were found to be higher in the filtrates than in the particles. Trichlorinated dibenzothiophenes and thianthrenes were found as the major congeners. Pentachlorinated derivatives were not found. Alkylated di- and trichlorodibenzothiophenes were detected in some samples, while alkylated chlorinated thianthrenes and diphenylsulfides were nondetectable. The estimated concentration levels of the compounds detected were in the range of 40–2700 pg/L in the pulp mill effluents and in the range of 2–40 pg/g dry weight in the sediments. Mixtures of methylated di- and trichlorodibenzothiophenes used as references in analyses were prepared from methylchlorobiphenyls. Some new pure model compounds were obtained by HPLC fractionation of the chlorination mixture of dibenzothiophene. Structures of these were determined by ¹H NMR.     

The metabolism of some chlorinated dibenzofurans by rats

Rats were given single oral doses of 2-chloro-, 2,8-dichloro-, 2,3,8-trichloro- and octachloro-dibenzofuran. Urine, faeces, fat and liver were analysed for starting materials and metabolites. The mono-, di- and trichlorodibenzofurans yielded mono- and dihydroxy derivatives, but metabolites containing sulphur were detected only with the mono- and dichlorodibenzofuran.Contrary to the chlorodibenzo-p-dioxins, where hydroxylated metabolites with substitution only at the 2,3-positions were isolated, chlorodibenzofuran-metabolites show a wider substitution pattern; five monohydroxy-derivatives were found, for instance, from 2,8-dichlorodibenzofuran.No metabolites were detected in urine, faeces and tissues of rats which were fed with octachlorodibenzofuran.     

Evaluation of retrofit crankcase ventilation controls and diesel oxidation catalysts for reducing air pollution in school buses

This study evaluates the effect of retrofit closed crankcase ventilation filters (CCFs) and diesel oxidation catalysts (DOCs) on the in-cabin air quality in transit-style diesel school buses. In-cabin pollution levels were measured on three buses from the Pueblo, CO District 70 fleet. Monitoring was conducted while buses were driven along their regular routes, with each bus tested three times before and three times after installation of control devices. Ultrafine number concentrations in the school bus cabins were 33–41% lower, on average, after the control devices were installed. Mean mass concentrations of particulate matter less than 2.5 μm in diameter (PM2.5) were 56% lower, organic carbon (OC) 41% lower, elemental carbon (EC) 85% lower, and formaldehyde 32% lower after control devices were installed. While carbon monoxide concentrations were low in all tests, mean concentrations were higher after control devices were installed than in pre-retrofit tests. Reductions in number, OC, and formaldehyde concentrations were statistically significant, but reductions in PM2.5 mass were not. Even with control devices installed, during some runs PM2.5 and OC concentrations in the bus cabins were elevated compared to ambient concentrations observed in the area. OC concentrations inside the bus cabins ranged from 22 to 58 μg m^?3 before and 13 to 33 μg m^?3 after control devices were installed. OC concentrations were correlated with particle-bound organic tracers for lubricating oil emissions (hopanes) and diesel fuel and tailpipe emissions (polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons). Mean concentrations of hopanes, PAH, and aliphatic hydrocarbons were lower by 37, 50, and 43%, respectively, after the control devices were installed, suggesting that both CCFs and DOCs were effective at reducing in-cabin OC concentrations.     

Pesticides in rainfall in Europe

Papers and published reports investigating the presence of pesticides in rainfall in Europe were reviewed. Approximately half of the compounds that were analysed for were detected. For those detected, most concentrations were below about 100 ng/l, but larger concentrations, up to a few thousand nanograms per litre, were detected occasionally at most monitoring sites. The most frequently detected compounds were lindane (gamma-HCH) and its isomer (alpha-HCH), which were detected on 90-100% of sampling occasions at most of the sites where they were monitored. For compounds developed more recently, detection was usually limited to the spraying season. A classification of pesticides according to their deposition pattern is proposed.     

Main products and kinetics of the thermal degradation of polyamides

The thermal degradation of the polyamides (PA) 6, 12, 66 and 612 was investigated by means of thermal analysis/mass spectrometry (TA-MS) and pyrolysis in a german standard oven. Sample masses were about 20 and 40 mg. The heating rates used in the dynamic studies were 1, 5 and 10 K min(-1). Both air and nitrogen atmospheres were utilized. The kinetic parameters were calculated from the TA-MS measurements and the main decomposition products were registered online. The evolved products from the pyrolysis oven were captured and analyzed off-line by GC/MS.     

Residual metal concentrations in soils and leaf accumulations in tobacco a decade following farmland application of municipal sludge

The objectives of this investigation were to examine the long-term residual effects of metal loading through sewage sludge applications on the total vs. diethylene triamine pentacetic acid (DTPA) extractable metal concentrations in soil and leaf accumulations in tobacco. Maryland tobacco (Nicotiana tabacum L.), cv. 'MD 609', was grown in 1983 and 1984 at two sites in Maryland that had been amended in 1972 with dewatered, digested sewage sludge from washington, DC, at rates equal to 0, 56, 112 and 224 mg ha(-1). The metal concentrations in the sludge, in mg kg(-1) dry weight, were: 1300 Zn, 570 Cu, 280 Pb, 45 Ni and 13 Cd. Soil samples collected from the surface horizon and composite leaf samples of cured tobacco were analyzed for total Zn, Cu, Mn, Fe, Pb, Ni and Cd concentrations. The soil samples were also examined for soil pH and DTPA extractable metals. Equations were generated using polynomic and stepwise regression analyses which described the relationships between total vs. DTPA extractable soil metals, and between DTPA soil and soil pH vs. plant metal concentrations, respectively. Significant increases were observed for both total and DTPA extractable metal concentrations for all metals, with all but total Mn and Ni being significant for linear and quadratic effects regarding sludge rates. However, linear relationships were found between DTPA extractable vs. total soil concentrations for all elements except Pb and Ni which were quadratic. Significant increases in plant Zn, Cu, Mn, Ni and Cd and decreases in Fe were observed with increased sludge rates. Plant Pb levels were unaffected by sludge applied Pb. Linear relationships were observed between plant Zn and Cd and DTPA soil metal levels: however, Mn and Cu levels were described by quadratic and cubic relationship, respectively. Relationships between plant Fe and Pb and DTPA extractable concentrations were nonsignificant. Additional safeguards to protect crop contamination from heavy metals such as Cd were discussed.     

Identification of volatile organic components in mussel

Volatile components in mussels were isolated by freeze vacuum distillation and over 100 components were identified by gas chromatography-mass spectrometry. Phenylalkanes were newly detected. Several halogenated compounds were observed.     

In situ and laboratory bioassays using Poecilia reticulata Peters, 1859 in the biomonitoring of an acidic lake at Camaçari, BA, Brazil

The suitability and viability of acute in situ bioassays were investigated in the biomonitoring program of an acidic lake contaminated with sulphur residues. Responses of organisms observed in laboratory and in situ bioassays were also assessed to determine whether or not they were similar and comparable, regarding accuracy and precision. Newborn Poecilia reticulata were employed as test organisms and exposed to the same water samples under in situ and laboratory conditions. Mortality/immobility was the endpoint assessed and dead/immobile organisms were counted at various time intervals during exposure. The mean calculated LT50 values and 95% confidence intervals were 1.61 (1.36-1.87) h in the laboratory bioassays and 0.72 (0.55-0.89) h in the in situ bioassays. Statistical comparison of these values revealed a significant difference (p<0.05). In situ bioassays were more accurate than those carried out in the laboratory, demonstrating higher sensitivity and better reproduction of what occurs in nature, while laboratory bioassays were more precise.