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.     

采出水中硫酸钙在膨润土表面的沉积过程

微生物在采出水处理中的应用越来越广泛,但污水中的硫酸钙等在微生物表面的沉积会降低微生物的处理效果。为了研究硫酸钙垢在颗粒表面的沉积过程,利用光学显微镜、激光粒度仪测定了硫酸钙垢在粘土颗粒表面的生长形态以及粒径的大小与时间的关系;通过溶液析晶过程中电导率的变化,探索了垢在表面反应阶段的结晶动力学;同时对垢沉积过程中Zeta电位的变化规律进行研究。结果表明,硫酸钙在膨润土表面反应阶段为一级反应,反应速率常数为0.00675 min-1;10 min以后电导率不变进入晶粒长大期。晶体在粘土表面沉积过程中颗粒呈现大小循环变化趋势,总体在9~17μm之间变化。硫酸钙在膨润土表面沉积过程的Zeta电位由最大值的-34.6 m V逐渐恒定到-5~-7 m V。     

用废玻璃和废铝制备耐磨复合材料的工艺研究

以废玻璃和废铝为原料,采用搅拌浇铸法制备玻璃/铝基废弃物复合材料.研究了玻璃颗粒形态、粒径、含量及制备工艺(温度、搅拌方式、时间)对复合材料微观组织和力学性能(如抗拉强度、耐磨强度)的影响.结果表明,玻璃颗粒较均匀地分布于铝基体中,界面结合良好;玻璃颗粒质量分数为10%～15%时,与铝基体相比,复合材料的耐磨性能提高较...     

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。     

基本单分散气溶胶透过率测试中真实值的计算

通过对高效、超高效滤料透过率测试台工作原理的分析得到:利用基本单分散粒子作为气溶胶测得的透过率关系与滤料真正的透过率-粒径曲线有区别,实际上是所使用实验气溶胶的综合透过率。详细研究了真正透过率与实验透过率的关系、误差和偏离产生原因,最终提出了一种独特的计算方法,实现了根据实验得到的表观透过率-粒径关系,就可以计算出真实透过率-粒径曲线,并得到了采用较为理想的实验气溶胶测试出的真实透过率的实际验证,这将大大提高高效、超高效滤料性能测试台的精度,拓展了其应用范围,为高效滤料的过滤理论和应用研究提供了比较理想的测试手段。     

好氧颗粒污泥强化解体实验与机理研究

在120r／min的搅拌及pH=1的强酸条件下,进行好氧颗粒污泥的强化解体实验,研究颗粒污泥的总数、平均粒径和粒径分布的变化情况。在15h实验时间内,搅拌强化解体的颗粒平均粒径从1230μm降至320μm,颗粒总数从30个／mL增至193个／mL。强酸强化解体结果类似,但解体时间为110h。搅拌比强酸对颗粒解体的强化作用更明显。粒径分布结果显示,小颗粒所占比例明显增加。颗粒解体过程中粒径分布均符合对数正态分布,但颗粒粒径的期望值石,随解体时间明显减小。根据颗粒的解体机理,即4种解体类型：破碎、破裂、剥落和研磨,结合实验结果,将解体过程分为对数期、平缓期、二次对数期和稳定期。     

超细无碱玻纤复合滤料的过滤性能

袋式除尘是一种高效的除尘技术,对PM_(2.5)具有较高的过滤效率,但是其运行阻力较大,因此,研发高效、低阻过滤材料是解决大气污染问题的关键所在。以耐高温的PPS纤维针刺布为上下层,超细无碱玻纤为中间层,经过超声波粘合或线缝合技术制备了多层复合过滤材料,研究了滤料在容尘状态下的过滤效率、过滤阻力,以及孔径变化。结果表明,该复合滤料的初始阻力低于150 Pa,容尘后对0.2~2μm的颗粒物的过滤效率达80%以上;随着粉尘的沉积,滤料的过滤效率有了较大提高,对1μm以上颗粒物的过滤效率可达99.99%以上,对最易透过粒径(MPPS)的过滤效率达95%以上;过滤前后,滤料的孔径分布发生了变化,过滤后滤料出现了1~5μm的孔径分布。该复合滤料在工业高温粉尘过滤中将会有较好的应用前景。     

活性炭负载I-TiO_2对气体中甲苯的吸附

利用溶胶凝胶-浸渍烧结法制备了碘掺杂二氧化钛修饰的活性炭复合吸附剂。利用XRD、SEM、BET、Boehm滴定、亚甲蓝吸附值等手段研究了活性炭负载前后表面结构与性质。利用动态吸附实验研究了活性炭负载I-TiO_2复合材料(IT/AC)和再生IT/AC对气体中甲苯的吸附。考察了活性炭粒径、气体的流速、吸附床层高度和气体中甲苯的浓度对活性炭吸附性能的影响及甲苯在活性炭固定床上的吸附动力学。结果表明:由于介孔I-TiO_2和活性炭的协同作用,负载适量I-TiO_2对活性炭结构和吸附性能影响较小。活性炭的粒径越小、复合材料的吸附穿透点和饱和吸附量越大;气体的流速和甲苯的初始浓度越大,复合材料的吸附穿透点越小但饱和吸附量越大。YOON-NELSON模型可以预测复合材料吸附甲苯的动力学过程。     

不同形态有机物对自我造粒流化床中颗粒特性的影响

研究了溶解态、胶体态及颗粒态有机物对自我造粒流化床中颗粒特性的影响.研究表明,有机物的形态对颗粒粒径和有效密度有较大影响,即溶解态有机物形成的颗粒粒径最小,胶体态有机物形成的颗粒粒径次之,颗粒态有机物形成的颗粒粒径最大;有效密度规律则相反.此外,颗粒的平均粒径、平均有效密度沿床层高度的变化有不同分布,即自我造粒流化床底部形成的颗粒有效密度最大,但同种原水水质条件下颗粒粒径没有变化规律.     

含重金属Cu元素模拟尘源气溶胶的试验研究

重金属元素易富集于大气颗粒物中且会对人体造成较大危害,为进一步提高高效空气过滤器性能,有针对性地去除含重金属元素的颗粒物,提出了有关过滤器测试标准要求外的新的人工尘源气溶胶发生溶液CuSO4,并从相关性、粒谱分布、分散度等方面对其能否满足测试气溶胶的要求进行验证分析。结果表明:(1)CuSO4和KCl间的相关系数(R2)为0.991 52,相关性很好;NaCl、KCl和CuSO4气溶胶的几何标准差分别为0.88、0.85、0.81,呈单分散且分散程度接近,可很好地满足测试气溶胶要求。(2)随发生溶液浓度的增加,气溶胶峰值粒径增大,导致分散度增加;随喷气压的增加,气溶胶峰值粒径减小,分布趋于集中。发生溶液浓度和喷气压对CuSO4和KCl气溶胶峰值粒径、粒子数浓度和分散度作用规律的一致性进一步证明了CuSO4气溶胶作为测试气溶胶的可行性。     

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.     

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.     

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.     

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.