基于GT-Power柴油机颗粒捕集器捕集性能的仿真研究

利用GT-Power软件建立了柴油机颗粒捕集器(DPF)仿真模型,进行了仿真计算。研究了颗粒捕集器本身结构参数对其捕集效率与压降的影响。结果表明,影响颗粒捕集器捕集效率的主要参数有通道密度(CPSI)、过滤体孔隙率、过滤体微孔直径以及过滤壁厚度;影响颗粒物压降的主要参数有通道密度、过滤体渗透率、过滤体孔隙率以及过滤壁厚度。     

不同横截面形状异形纤维捕集颗粒物的数值模拟

基于离散相模型(DPM),模拟研究了不同横截面形状异形纤维在拦截和惯性碰撞2种机制下对颗粒物的捕集效率;考察了颗粒物粒径、入口风速、纤维填充率和纤维放置方式对不同横截面形状异形纤维捕集颗粒物效率的影响。结果表明,当颗粒物粒径为0.5~2.5 μm,入口风速为0.5 m·s⁻¹时,异形纤维对颗粒物的捕集效率随粒径的增加而增加,对粒径为1.5 μm及以上颗粒物的捕集效率明显增加;入口风速为0.2~0.6 m·s⁻¹时,颗粒物粒径为2.5 μm时,异形纤维对颗粒物的捕集效率均随入口风速的增加而增加;当填充率为1.2%~4.0%时,颗粒物粒径为2.5 μm时,异形纤维对颗粒物的捕集效率随填充率的增加而增加,其中横截面为正三角形的纤维对颗粒物的捕集效率均最大。异形纤维的径向异形度相同时,纤维边垂线与来流方向平行的放置方式对颗粒物的捕集效率较高。不同横截面形状异形纤维的径向异形度系数越小,对颗粒物的捕集效率受纤维的放置方式的影响越小。本研究可为新型纤维滤料的开发提供参考。     

布袋过滤除尘中气固两相流的格子Boltzmann模拟

使用格子Boltzmann方法对含尘气体通过布袋滤料纤维的流动进行了数值模拟,采用拉格朗日方法跟踪了颗粒相中每个粒子的位置和速度并进行单向耦合计算。分析了气流通过纤维捕集体过程中的压降的变化规律,结果与达西渗透定律吻合。与此同时,对粒径小于1μm的气溶胶粒子在布袋纤维捕集体上的沉积规律展开了讨论。结果表明,粒径小于0.01μm的粒子的捕集主要受粒子的布朗随机扩散效应的控制;粒径大于0.1μm的粒子则主要依靠纤维滤料的拦截作用而沉积在捕集体表面;而粒径在0.01～0.1μm范围的粒子则具有较低的捕集效率。模拟结果为研究袋式除尘的过滤机理提供了依据。     

粉尘颗粒在单纤维表面沉积的计算机模拟

采用随机模拟方法模拟研究了粉尘颗粒在单纤维表面上的沉积过程,Kuwabara流场用于计算粉尘颗粒运动的轨迹,模拟中考虑了粉尘颗粒的粒径分布和单纤维在气流作用下的扭曲行为对粉尘颗粒沉积的影响.模拟结果表明.粉尘颗粒在单纤维表面上的沉积形态与分布特征依赖于Stokes数、粉尘颗粒粒径分布和纤维扭曲程度;模拟获得的粉尘树枝结构与相关文献提供的实验结果相似.     

柴油机微粒捕集器复合再生性能及其场协同分析

基于柴油机微粒捕集器瞬态复合再生机理,建立了CFD三维仿真模型,并利用漩涡破碎燃烧模型和场协同数学模型对柴油机微粒捕集器瞬态复合再生过程的速度矢量和温度梯度进行了数值模拟和场协同分析,结果表明,再生时间为175 s时的微粒捕集器过滤体后端壁面峰值温度达到1 184 K,且其过滤体内速度矢量和温度梯度的协同度最好,最优燃烧再生区域所占最大比值为0.58,表明此时微粒捕集器过滤体内再生燃烧速率最大,其再生效率最高。     

料屉式颗粒床对高温含尘烟气的过滤特性

采用料屉式颗粒床过滤装置对工业生产过程中产生的高温烟气处理问题进行研究。装置包括粉尘输送装置和颗粒床过滤装置两部分,其中过滤装置采用分层料屉,可观察单层料屉粉尘捕集情况。考察了烟气温度、凝尘添加比例和滤料颗粒粒径等因素对颗粒床过滤特性的影响。结果表明：随烟气温度逐渐升高至凝尘熔点、滤料颗粒粒径的减小以及凝尘添加比例的增加,床层过滤效率及压降均会上升,颗粒床出口处粉尘浓度不断降低;其中凝尘添加比例对于过滤特性影响最显著。在实验范围内最佳过滤条件下,颗粒床过滤效率最高可达99.40%,出口处烟气质量浓度低至12.02 mg·m⁻³。通过考察首层料屉滤料表面粉尘粘结形貌,发现滤料层粘结面呈现“由中心向四周发散”的整体格局,颗粒表面有“锥形”粘结层出现。本研究结果可为提升料屉式颗粒床过滤除尘器的除尘功效提供参考。     

高炉除尘灰细微颗粒物单/双预荷电强化滤袋过滤特性

传统袋式除尘器对于细微颗粒物的捕集效率不甚理想,在袋式除尘器入口前增加预荷电装置是一种切实可行的强化其过滤特性的技术手段。设计搭建线板式直流高压预荷电器,研究了不同正/负匹配电压及风速对于双极预荷电高炉除尘灰电凝并行为的影响规律,对比分析了滤袋对未荷电、单极负荷电以及双极荷电高炉除尘灰细微颗粒物 (PM _2.5) 的捕集效率与压差特性,得到了不同预荷电方式高炉除尘灰细微颗粒物在滤袋表面沉积的微观形貌结构。结果表明：随着过滤风速 (1.5~0.5 m·s⁻¹及匹配负电压 (−16~−12 kV) 的降低,双极荷电颗粒物凝并效率提高;高炉除尘灰细微颗粒物单/双预荷电均能提高滤袋的过滤效率;对于粒径＜0.5 μm颗粒,双极预荷电技术对滤袋捕集效率的强化效果好于单极预荷电技术;对粒径为0.5~2.5 μm颗粒,单极预荷电技术的强化效果超过了双极预荷电技术;颗粒物单/双预荷电技术还使得滤袋阻力增量值及其增长速率值降低,且单极预荷电技术对于阻力降低效果更为明显。本研究可为利用单/双预荷电技术提升传统袋式除尘器对高炉除尘灰中细微颗粒物的捕集脱除特性提供参考。     

PPS滤布对柴油机排放PM的过滤效率

基于柴油机实验台架和颗粒捕集装置,采用聚苯硫醚(PPS)针刺毡滤布过滤柴油机排放的颗粒物(PM)。利用称重法,以Whatman玻璃纤维滤纸为对比滤纸,间接测试了3种PPS滤布的过滤效率;同时实验探索了表面涂覆聚四氟乙烯的PPS滤布的深床过滤时间。实验结果表明,3种滤布在180℃的加热条件下将出现颜色和形态的变化;3种滤布在深床过滤期对PM的平均过滤效率分别为78.8%、76.9%和83.7%;表面涂覆聚四氟乙烯的PPS滤布的深床过滤时间为15~20 min,此后其过滤效率可接近100%。     

孔道结构对柴油机微粒捕集器工作特性的影响

针对柴油机微粒捕集器中灰烬颗粒的沉积特征,设计了一种非对称孔道微粒捕集器,基于非对称孔道微粒捕集器对微粒捕集器再生模型进行修正,分析了非对称孔道对微粒捕集器再生特性的影响。研究结果表明,增大过滤体进出口截面比能减少微粒捕集器的压力损失,降低碳烟再生时过滤壁面的最大温度,且非对称孔道能减少灰烬沉积对再生时壁面最大温度的影响,因此根据过滤体壁面厚度适当增大进出口孔道截面比可以有效提升过滤体的碳烟承载量,延长微粒捕集器的车载使用寿命。     

新型电袋复合除尘器性能研究

为了提高布袋除尘器对细微粒子的捕集效率,同时降低压力损失,提出了一种新型的电袋复合除尘器,并利用这种新型的除尘器对2 500目的超细滑石粉进行了实验研究。通过普通布袋过滤、电袋复合过滤的对比实验研究,得到了电场强度、气布比、压损、清灰周期和除尘效率等参数的变化规律。实验结果表明,使用新型的复合除尘器过滤粉尘时,粉尘在进入袋室之前就被荷电,通过在滤料表面施加较强的静电场,使得被处理粉尘在滤料的表面有序堆积和排列,能有效地降低压力损失,提高过滤风速,除尘效率均达到97%以上。Vf=3.5 m/min,U=12.3 kV时,新型复合除尘器与普通布袋过滤相比压力损失降低了90 Pa;PM2.5的捕集效率提高了5.9%;清灰周期从10 min延长至36 min。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

The variation of street air levels of PAH and other mutagenic PAC in relation to regulations of traffic emissions and the impact of atmospheric processes

The occurrence of particle associated PAH and other mutagenic PAC was determined in 1996 in the street air of Copenhagen. In addition, particle extracts were tested for mutagenicity. The measurements were compared with previous measurements in 1992/1993. The levels had decreased in this period. The decrease was caused by an implementation of light diesel fuels for buses and the exchange of older petrol-driven passenger cars with catalystequipped new ones. About 65% of the reduction was caused by the application of the light diesel fuels. Under special conditions, chemical processes in the atmosphere produced many more mutagens than the direct emissions. The concentrations of S-PAC and N-PAC were 10 times lower than those of PAH, while the levels of oxy-PAH were in the same order of magnitude as those of PAH. Benzanthrone, an oxy-PAH, is proposed to be formed in the atmosphere in addition to direct emissions. Benzo(a)pyrene, often applied as an air quality criteria indicator, was photochemically degraded in the atmosphere. A strong increase in the mutagenic activities was observed to coincide with a depletion of benzo(a)pyrene.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

Teratological effects of pesticides in vertebrates: a review

Abstract

In the last decades, the use and misuse of pesticides in the agriculture have increased, having a severe impact on ecosystems and their fauna. Although the various effects of pesticides on biodiversity have been already documented in several studies, to our knowledge no consistent overview of the impact of pesticides in vertebrates, both terrestrial and aquatic, is available. In this review, we try to present a concise compilation of the teratogenic effects of pesticides on the different classes of vertebrates – mammals, birds, reptiles, amphibians and fish.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.