Factors affecting oxygen-transfer rates in headspace-gas respirometers.

Satisfactory measures of the biological-oxygen-uptake rate in headspace-gas respirometers can only be achieved if the rate of oxygen transfer from the headspace gas to liquid is greater than the rate of oxygen uptake by microorganisms. In the authors' study, factors potentially affecting oxygen-transfer limitations in headspace-gas respirometers were evaluated quantitatively. Tests were conducted to measure maximum-oxygen-uptake rates by operating a respirometer under various test conditions. Analysis of respirometric data indicated that limiting oxygen-transfer rates were related to mixing intensity, length of magnetic stirring bar, volume of sample, and oxygen content in the headspace gas. A multivariable model was developed to describe the overall contribution of these factors to the limiting oxygen-transfer rate. This model should be useful for estimating maximum-oxygen-transfer rates for essentially all headspace-gas respirometers.     

非稳定状态下除磷过程的特点研究

为了研究非稳定状态下生物除磷的特点,采用序批式间歇反应器(SBR),通过不同的进水方式(连续进水和瞬时进水),系统地考察了进水体积、NOX-N、限制曝气等因素对除磷过程的影响。结果表明,在温度为(23±0.5)℃、pH为7.0～8.0时,厌氧搅拌期连续进水的比释磷量(单位质量污泥(以MLSS计)的释磷量(以PO43-P计))比瞬时进水时高出42.11%。在运行条件相似的情况下,厌氧搅拌期的比释磷量与每周期进水体积无关。相对于连续进水,瞬时进水更有助于促进微生物利用有机底物进行自身的生长。限制曝气对连续进水和瞬时进水的释磷过程都存在明显的影响,在DO小于0.1mg/L的情况下,2者的比释磷量相对非限制曝气时分别降低了57.14%和55.56%。在连续进水时,NOX-N的反硝化结束伴随着释磷速率的突然升高。利用贮存作用并不能每次都成功地抑制丝状菌污泥膨胀。     

Comparison of PM2.5 carbon measurement methods in Hong Kong, China

Samples from Hong Kong, China, were analyzed for organic carbon (OC), elemental carbon (EC), and total carbon (TC) by three thermal protocols (low-temperature IMPROVE and high-temperature STN and NIOSH) and two optical monitoring methods: reflectance and transmittance. Good agreement (+/-10%) for TC among the three protocols was observed for sample loadings of 1-55 microg m(-3). The two protocols using a reflectance pyrolysis correction showed best agreement for EC, with <20% differences found for approximately 80% of the samples. Hong Kong has a large diesel fleet, and for some heavily loaded samples the light transmittance was too low for quantitative detection, resulting in large uncertainties in the OC/EC split based on transmittance. Hong Kong experienced OC levels similar to those at US sites, but has much higher EC concentrations. OC/EC ratios range from 2 to 5 at two US sites and from 0.2 to 1.2 at three Hong Kong sites.     

Comparison of experimental ponds for the treatment of dye wastewater under controlled and semi-natural conditions

This study compares the performance of simulated shallow ponds vegetated with Lemna minor L. under controlled and semi-natural conditions for the treatment of simulated wastewater containing textile dyes. The objectives were to assess the water quality outflow parameters, the potential of L. minor concerning the removal of chemical oxygen demand (COD) and four azo dyes (Acid blue 113, reactive blue 198, Direct Orange 46 and Basic Red 46) and the plants’ growth rate. Findings show that all mean outflow values of COD, total dissolved solids (TDS) and electrical conductivity (EC) were significantly (p < 0.05) lower within the outdoor compared to the indoor experiment except the dissolved oxygen (DO). The COD removal was low for both experiments. The outflow TDS values were acceptable for all ponds. The pond systems were able to reduce only BR46 significantly (p < 0.05) for the tested boundary conditions. Removals under laboratory conditions were better than those for semi-natural environments, indicating the suitability of operating the pond system as a polishing step in warmer regions. The mean outflow values of zinc and copper were below the thresholds set for drinking and irrigation waters and acceptable for L. minor. The dyes inhibited the growth of the L. minor.     

Combustion sources of particles: 2. Emission factors and measurement methods

Emissions from the combustion of biomass and fossil fuels are a significant source of particulate matter (PM) in ambient outdoor and/or indoor air. It is important to quantify PM emissions from combustion sources for regulatory and control purposes in relation to air quality. In this paper, we review emission factors for several types of important combustion sources: road transport, industrial facilities, small household combustion devices, environmental tobacco smoke, and vegetation burning. We also review current methods for measuring particle physical characteristics (mass and number concentrations) and principles of methodologies for measuring emission factors. The emission factors can be measured on a fuel-mass basis and/or a task basis. Fuel-mass based emission factors (e.g., g/kg of fuel) can be readily used for the development of emission inventories when the amount of fuels consumed are known. Task-based emission factors (g/mile driven, g/MJ generated) are more appropriate when used to conduct comparisons of air pollution potentials of different combustion devices. Finally, we discuss major shortcomings and limitations of current methods for measuring particle emissions and present recommendations for development of future measurement techniques.     

Effect of reducing conditions on sludge melting process

The objective of this study was to compare the effects of CO/CO(2) reducing conditions with those of air oxidizing conditions on the pouring temperature of the sludge melting process and the heavy metal leachability of the resultant sludge slag. Synthetic sludge ash composed of SiO(2), CaO and Al(2)O(3), as well as sewage sludge ash generated from a laboratory incinerator was employed. The experimental results indicated that the pouring temperatures are significantly reduced under the reducing conditions of CO/CO(2), or 24 and 77 degrees C lower than under air conditions for synthetic and sludge ash, respectively. The heavy metal leaching tests further indicate lower heavy metal concentrations present in the leachate under the reducing conditions, notably an order of magnitude lower in Zn. However, X-ray diffractogram indicates similar peaks for these two slags produced under different conditions.     

Shewanellasp．XB缺氧反硝化降解苯酚

苯酚的生物降解一直受到关注。以苯酚为惟一电子供体,研究了Shewanellasp．XB对苯酚的缺氧降解特性。研究结果表明,在反硝化条件下,当C／N为13．3时,苯酚可以完全降解,NO2--N积累量很少。另外,当加入氧化还原介体,如核黄素3μmol／L、AQDS0．01mmol／L、AQS0．05mmol／L和LQ0．01mmol／L时,苯酚降解速率分别为不加介体时的1．45、1．77、1．67和1．63倍。当以氯化铵代替硝酸盐时,苯酚也能进行厌氧发酵降解。另外,菌株XB反硝化降解苯酚可能是厌氧和好氧降解的混合过程。     

Degradation of herbicides in two sandy aquifers under different redox conditions.

We examined the potential for complete degradation (mineralisation) of the four [ring-U-14C]herbicides mecoprop, isoproturon, atrazine, and metsulphuron-methyl in two sandy aquifers representing aerobic, denitrifying, sulphate-reducing, and methanogenic conditions. Slurries with sediment and groundwater were set-up aerobically or anaerobically in the presence of the electron-acceptor prevailing at the sampling site, amended with 25 microg l(-1) herbicide, and incubated at 10 degrees C. Considerable mineralisation was only observed in sediment from the plough layer incubated aerobically. Here, 30% of 14C-mecoprop was recovered as 14CO2 after 15 days and 15% of isoproturon was recovered as 14CO2 after 267 days. Only 7% of mecoprop was recovered as 14CO2 after 313 days in sediment from the aquifer below sampled at 1.95-3.00 mbs (m below the surface). In denitrifying and methanogenic slurries, 3% of 14C added as mecoprop was recovered as 14CO2. Isoproturon was not mineralised except in the aerobic plough layer, and atrazine and metsulphuron-methyl were not mineralised under any of the conditions applied.     

Comparison of the droplet size spectra produced by rotary atomizers and hydraulic nozzles under simulated aerial application conditions

Abstract

A wind tunnel was used to characterize the droplet size spectra of liquid sprays from several different atomizers and nozzles used under simulated aerial application conditions. The atomizers included a D8–46 nozzle, a Through Valve Boom (TVB) nozzle, and rotary cage and drum atomizers.

The D8–46 hydraulic nozzle was evaluated, using water, at orientations of 0, 10, 20, 30, 40, 50, 60, 70, 80 and 90° relative to 145 and 180 km/h airstreams. The TVB nozzle was evaluated using water, water with isopropyl alcohol, and water with a non‐ionic surfactant at airstream velocities between 130 and 180 km/h. The rotary atomizers were evaluated at different rotation rates, flow rates of water and an insecticide, in 130 and 180 km/h airstreams.

The volumetric droplet size spectra parameters (D_vo.x) decreased as the angle of the D8–46 nozzle and the airstream velocity increased. Empirical models were developed to predict these values for different windspeed and nozzle angle conditions. The TVB nozzle produced larger droplets than the other atomizers under similar conditions, with a decrease in the D_vo.x parameter values as the airstream velocity increased.

The D_vo.x parameter values produced by the rotary atomizers increased as the liquid flow rate increased, and as the rotation rate and airstream velocity decreased, and were lower for the insecticide than for water. The slotted rotary drum atomizer gave the best control over droplet size, generally producing mono‐modal droplet size spectra where the other atomizers often produced bi‐ and multimodal spectra.     

Prediction of bioconcentration factors under non-equilibrium conditions

With the bioconcentration of lipophilic compounds by aquatic organisms when equilibrium between water and biota is attained, the logarithm of the bioconcentration factor has a direct linear relationship with the logarithm of the octanol/water partition coefficient. In practice, however, equilibrium may not be reached, particularly for more lipophilic compounds. It is shown theoretically, and confirmed by use of published experimental results on fish, that a different direct linear relationship also exists between the logarithms of the bioconcentration factor and the partition coefficient for compounds not achieving equilibrium after a specific exposure time. Thus, non-equilibrium bioconcentration factors can be predicted from their partition coefficients. The constants in the non-equilibrium linear equation are related to those from the relationships between equilibrium bioconcentration factors and the partition coefficients, and between the first-order clearance rate constants and the partition coefficients.     

硫酸盐还原条件下三氯乙烯的降解研究

三氯乙烯(TCE)是地下水和土壤中主要的有机污染物之一.以受TCE等氯代烃严重污染的地下泥样为材料,采用室内模拟的方法.研究硫酸盐初始质量浓度为100、500、2 500 mg/L时.硫酸盐对TCE降解的影响.结果表明.高浓度硫酸盐更有利于TCE的降解;在硫酸盐还原条件下,通过添加2-溴乙基磺酸钠抑制产甲烷菌.发现产甲烷菌在TCE的降解过程中起到很重要的作用;硫酸盐浓度变化与TCE降解趋势一致.     

Metabolism of fluvalinate in chickpea plants under sub-tropical conditions of northern India.

The metabolism of fluvalinate in chickpea plants in the field under sub-tropical climatic conditions has been investigated. Ten days after spraying with fluvalinate, leaves were collected and extracted in acetone. The extract was fractionated and the metabolites were identified by co-chromatography using TLC, GLC, and GC-MS. The anilino acid, a metabolite derived from ester cleavage, was the major metabolite present as both free and conjugated forms in chickpea leaves. 3-PBacid and 3-PBalc were minor metabolites. Glucose was found to be the major sugar conjugating with the metabolites.     

Fate and transport of N-nitrosamines under conditions simulating full-scale groundwater recharge operations.

The key objective of this study was to investigate the attenuation mechanisms of seven N-nitrosamine compounds at environmental concentrations and under conditions relevant to groundwater recharge operations. The study used a combination of controlled laboratory-scale soil-column experiments and groundwater monitoring at a full-scale river-bank filtration facility. Findings of the controlled column experiments suggest that N-nitrosodimethylamine and six other N-nitrosamines (N-nitrosodiethylamine, N-nitrosomethylethylamine, N-nitroso-n-propylamine, N-nitrosodi-n-butylamine, N-nitrosopiperidine, and N-nitrosopyrrolidine) are biodegradable under oxic and anoxic oxidation-reduction conditions. Half lives determined in this study for the targeted compounds varied between 1.3 and 7 days, which will ensure a removal to below detection limits (< 2 ng/L) within short travel times in groundwater recharge systems. Findings of this study suggest that complete removal of N-nitrosamines requires the presence of an adapted biocommunity, which will be established over several weeks to months.     

Biological decolorization of reactive anthraquinone and phthalocyanine dyes under various oxidation-reduction conditions.

The decolorization of two anthraquinone dyes (Reactive Blue 4 [RB4] and Reactive Blue 19 [RB19]) and two phthalocyanine dyes (Reactive Blue 7 [RB7] and Reactive Blue 21 [RB21]) was investigated at an initial dye concentration of 300 mg/L using an unacclimated, enrichment culture. The culture was fed a mixture of organic compounds and maintained initially under aerobic conditions, and then progressively developed anoxic/ anaerobic conditions. Biotransformation-related decolorization of the dyes did not take place under aerobic conditions, but use of the feed organic mixture and biomass production by the enrichment culture were not affected. Complete ammonia removal occurred in the control and all dye-amended cultures. The development and extent of nitrification were much lower in the latter cultures, in which ammonia removal via air stripping was the dominant mechanism. Prolonged incubation of the culture under anoxic/anaerobic conditions with multiple carbon source additions resulted in a high decolorization extent of anthraquinone dyes (over 84%) and only partial decolorization of phthalocyanine dyes (49 to 66%). Development of significant methanogenic activity took place in the control and, to a lesser extent, in the two phthalocyanine dye-amended cultures, but the anthraquinone dyes severely inhibited the development of methanogenic activity. The RB4 and RB19 decolorization was attributed to nonreversible, microbially mediated dye transformation(s), demonstrated by the accumulation of decolorization products with absorbance maxima in the 420- to 460-nm region. The decolorization of RB4 and RB19 followed Michaelis-Menten kinetics. At an initial dye concentration of 300 mg/L, the observed maximum decolorization rate per unit biomass was 9.1 and 37.5 mg dye/mg volatile suspended solids x day for the RB4 and RB19, respectively. Thus, partial decolorization of reactive phthalocyanine dyes and extensive biological decolorization of reactive anthraquinone dyes is feasible only under anoxic/anaerobic conditions.     

Evaluation of VOC emission measurement methods for paint spray booths

Interest in regulations to control solvent emissions from automotive painting systems is increasing, especially in ozone nonattainment areas. Therefore, an accurate measurement method for VOC emissions from paint spray booths used in the automotive industry is needed to ascertain the efficiency of the spray booth capture and the total emissions. This paper presents the results of a laboratory study evaluating potential VOC sampling and analytical methods used in estimating paint spray booth emissions, and discusses these results relative to other published data. Eight test methods were selected for evaluation. The accuracy of each sampling and analytical method was determined using test atmospheres of known concentration and composition that closely matched the actual exhaust air from paint spray booths. The solvent mixture to generate the test atmospheres contained a large proportion of polar, oxygenated hydrocarbons such as ketones and alcohols. A series of identical tests was performed for each sampling/analytical method with each test atmosphere to assess the precision of the methods. The study identified significant differences among the test methods in terms of accuracy, precision, cost, and complexity.     

Comparison of translocation methods to conserve metallophyte communities in the Southeastern D.R. Congo

In southeastern Democratic Republic of Congo, unique metallophyte communities supporting numerous endemic species occurred on the highly mineralized copper cobalt (Cu–Co) hills throughout the province. These hills are economically valuable mineral reserves; mining activities represent therefore a threat to the long-term persistence of these communities. Ex situ conservation program was set up by a mining company to rescue and conserve the diversity of Cu–Co communities until restoration activities are initiated. Two kinds of Cu–Co communities: the steppe and the steppic savanna, were translocated using topsoil spreading and whole-turf translocation. In this study, we assessed the effectiveness of these two techniques in conserving Cu–Co communities and their potential use in future restoration programs. More than 2 years after the translocation, whole-turf translocation appeared to be the better technique for ex situ conservation of endemic Cu–Co species. Not only did whole-turf successfully translocate numerous target species that were not present in the topsoil areas, but it also resulted in fewer ruderal and non-target species compared to topsoil spreading. Topsoil spreading recorded low seedling emergence from seed bank due to large proportions of dormant seeds or the absence of a seed bank, especially for the steppic savanna. Restoration of the steppe is currently more successful than for steppic savanna where the lack of dominant and structuring species likely contributed to divergence in species composition compared to reference ecosystem. Our study stresses the fact that tropical old-growth grasslands, which require probably several centuries to assemble, are difficult to restore or translocate.     

Comparison of two methods for obtaining degradation half-lives

Given the paucity of experimental degradation half-life data for most organic chemicals, there is a compelling incentive to use available estimation software when undertaking assessments of chemical persistence and mass balance modeling studies. In this study, half-life data obtained from estimation software for a set of 233 organic chemicals in air, water, soil and sediments were shown to differ significantly from half-life data listed in handbooks. It is suggested that the widely available and used estimation software, EPIWIN (Estimations Program's Interface for Windows), overestimates the reactivity of persistent organic pollutants (POPs). Reasons for this overestimation are explored. It is concluded that the maximum "default half-life values" used by the EPIWIN software are too short for estimating half-lives of highly persistent chemicals such as PCBs. There is a need for estimation software such as EPIWIN to be more thoroughly calibrated against experimental derived half-life data for a wide range of chemicals, including potential POPs, thus improving their reliability.     

Formaldehyde emission—Comparison of different standard methods

The emission of formaldehyde is an important factor in the evaluation of the environmental and health effects of wood-based board materials. This article gives a comparison between commonly used European test methods: chamber method [EN 717-1, 2004. Wood-based panels—determination of formaldehyde release—Part 1: formaldehyde emission by the chamber method. European Standard, October 2004], gas analysis method [EN 717-2, 1994. Wood-based panels—determination of formaldehyde release—Part 2: formaldehyde release by the gas analysis method, European Standard, November 1994], flask method [EN 717-3, 1996. Wood-based panels—determination of formaldehyde release—Part 3: formaldehyde release by the flask method, European Standard, March 1996], perforator method [EN 120, 1993. Wood based panels—determination of formaldehyde content—extraction method called perforator method, European Standard, September 1993], Japanese test methods: desiccator methods [JIS A 1460, 2001. Building boards. Determination of formaldehyde emission—desiccator method, Japanese Industrial Standard, March 2001 and JAS MAFF 233, 2001] and small chamber method [JIS A 1901, 2003. Determination of the emission of volatile organic compounds and aldehydes for building products—small chamber method, Japanese Industrial Standard, January 2003], for solid wood, particleboard, plywood and medium density fiberboard.The variations between the results from different methods can partly be explained by differences in test conditions. Factors like edge sealing, conditioning of the sample before the test and test temperature have a large effect on the final emission result. The Japanese limit for F **** of 0.3 mg l⁻¹ (in desiccator) for particleboards was found to be equivalent to 0.04 mg m⁻³ in the European chamber test and 2.8 mg per 100 g in the perforator test. The variations in inter-laboratory tests are much larger than in intra-laboratory tests; the coefficient of variation is 16% and 6.0% for the chamber method, 25% and 3.5% for the gas analysis method and 15% and 5.2% for the desiccator method.     

Evaluation of TCDD biodegradability under different redox conditions

Polychlorinated dibenzo-p-dioxins have been generated as unwanted by-products in many industrial processes. Although their widespread distribution in different environmental compartments has been recognized, little is known about their fate in the ultimate environment sinks. The highly stable dioxin isomer 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) has been called the most toxic compound known to man. In this laboratory microcosm study, TCDD bioavailability was evaluated under five reduction/oxidation (redox) conditions including aerobic biodegradation, aerobic cometabolism, methanogenesis, iron reduction, and reductive dechlorination. Activated sludge and aquifer sediments from a TCDD and a pentachlorophenol (PCP) contaminated site were used as the inocula. Acetate, sludge cake, and cane molasses were used as the primary substrates (carbon sources) in cometabolism and reductive dechlorination microcosms. After a 90-day incubation period, microcosms constructed under reductive dechlorination conditions were the only treatment showing promising remediation results. The highest TCDD degradation rate [up to 86% of TCDD removal (with an initial concentration of 96 microg/kg of soil)] was observed in the microcosms with anaerobic activated sludge as the microbial inocula and sludge cakes as the primary substrates. Except for reductive dechlorination microcosms, no significant TCDD removal was observed in the microcosms prepared under other conditions. Thus, application of an effective primary substrate to enhance the reductive dechlorination process is a feasible method for TCDD bioremediation. Bioremediation expense can be significantly reduced by the supplement of some less expensive alternative substrates (e.g., sludge cakes, cane molasses). Results would be useful in designing a scale-up in situ or on-site bioremediation system such as bioslurry reactor for field application.     

Assessment of stream biological responses under multiple-stress conditions

Background, aim and scope  

Due to the numerous anthropogenic stress factors that affect aquatic ecosystems, a better understanding of the adverse consequences on the biological community of combined pressures is needed to attain the objectives of the European Water Framework Directive. In this study we propose an innovative approach to assess the biological impact of toxicants under field conditions on a large spatial scale.