ESP粉尘收集性能的影响因素

为了进一步提高电除尘器的收尘效率,尤其是对高比电阻粉尘的收尘效率,依据非稳态静电收集理论,对影响电除尘器粉尘收集性能各项因素的作用程度及机理进行了进一步研究。实验研究了粉尘收尘效率与不同比电阻粉尘的最优极间距、最优工作电压、粉尘层厚度和比电阻之间的相互关系。研究结果表明,随着极间距的增加,对应比收尘极面积,对于不同比电阻粉尘的收尘效率的增加幅度是不同的,其中高比电阻粉尘的收尘效率增加的趋势更加显著;粉尘比电阻越高,所对应的最优极间距越大,宽间距电除尘器对捕集高比电阻粉尘具有一定优越性;在最优极间距条件下,粉尘比电阻越高,其所对应的最优工作电压越小;相对于正常比电阻粉尘,随极板沉积粉尘层厚度的增加,高比电阻粉尘的最佳收尘效率所对应的最优工作电压升高幅度较大,而且最优工作电压所对应的收尘效率下降显著。随粉尘比电阻的增大,电除尘器收尘效率逐渐降低,特别是当粉尘比电阻大于1011Ω.cm后,粉尘收尘效率显著下降。研究结果与非稳态静电收尘理论提出的观点相吻合,有助于透彻理解电场结构和运行参数与粉尘收集性能的关系,特别是对于今后研发提高高比电阻粉尘收集性能的针对性技术措施具有指导作用。     

直筒式旋风脉冲静电除尘器性能研究

实验研究了电压、入口粉尘浓度和入口风速对直筒式旋风脉冲静电除尘器除尘效率的影响,测定了在不同入口风速下除尘器的分级效率.结果表明,脉冲供电能显著提高除尘器的除尘效率和分级效率,在脉冲电压为80 kV、入口粉尘质量浓度为5.0 g/m3N、入口风速为7～10 m/s时,除尘效率在99%以上,并在实验的基础上分析了脉冲供电下除尘器的除尘机理.     

公路隧道空气颗粒物净化实验研究

研制了窄极距双区电除尘公路隧道空气颗粒物净化系统,研究了粉尘浓度、粉尘粒度、工作电压及电场风速等主要因素对其净化性能的影响。结果表明,该技术方案可行,颗粒物净化效率随粉尘浓度及电场风速增大而降低,随工作电压及粉尘粒径增高而提高。     

荷电水雾除尘器捕尘效率的实验研究

实验分析了影响荷电水雾除尘器除尘效率的主要因素,在此基础上提出了一种新的除尘效率数学模型,该模型明确地表达了过滤风速、喷雾量以及雾滴荷质比对除尘效率的贡献情况。对实验结果及数学模型的分析表明,对于带有振弦栅的荷电水雾除尘系统,喷雾量对除尘效率的影响比过滤风速及荷质比更为显著,新除尘效率模型的提出对指导生产具有重要意义。实验中同时确定了荷电水雾除尘器最佳操作参数,在粉尘入口浓度为412 mg/m3的情况下,当过滤风速为16 m/s,喷雾量为12×10-3 m3/min,雾滴荷质为3.5×10-4 c/kg时,除尘效率可达99.5%。     

原煤暗道通风除尘特征参数的数值模拟及优化

为了掌握输煤过程中原煤暗道粉尘运移扩散规律,确定最优排尘风速,进行通风除尘系统优化改造研究.以中煤平朔木瓜界选煤厂133暗道为研究背景,根据气固两相流理论,利用离散相模型对原煤暗道空间粉尘浓度进行了数值模拟,并与现场实际分布情况进行对比分析,模拟结果与实测数据基本一致.研究结果表明,暗道空间内皮带机尾及导料槽出口处粉尘浓度较大,并以给料机及机尾为中心径向逐步降低;最优排尘风速为2 m/s时,粉尘浓度下降幅度能达到97.2％,降尘效果显著,暗道空间内粉尘浓度保持在4 mg/m3以内.     

双区式电凝并技术对提高细微粉尘凝并效率的影响

为了进一步提高电凝并装置对细微粉尘的凝并效率,降低细微粉尘对人体的危害,设计一种由双极芒刺预荷电区和平行板收尘区组成的双区芒刺式电凝并装置,通过实验探究了安装双区芒刺预荷电装置、极配间距、外加电压3个凝并参数对细微粉尘凝并效率的影响。结果表明:当外加电压≤13 kV时,细微粉尘的凝并效率随外加电压的升高而增大,而当外加电压13 kV时,电凝并效率无明显提高;安装双极芒刺预荷电装置和缩短极配间距都可以有效提高细微粉尘凝并效率,当外加电压为13 kV时,极配间距由0.03 m缩短至0.02 m,各粒径粉尘的凝并效率均有10%以上的提高。根据实验结果可以得出,细微粉尘电凝并最优实验参数为安装双极芒刺预荷电装置、极配间距0.02 m、外加电压13 kV。以上研究结果可为电凝并技术的推广及工业应用提供参考。     

SZD组合电收尘器在回收水泥粉尘中的应用

组合式电收尘系将电旋风、电抑制、电凝聚等三种复式收尘机理组合为一体，兼具电器和机械收尘的最佳特性，在捕集高浓度高比电阻、微颗粒粉尘等工业收尘中以高效可靠，结构简便，价格便宜，维修方便等优点深受广大用户欢迎。     

双极电袋复合除尘器的增效减阻效应

为提高现有电袋复合除尘器的除尘效率,降低压力损失,改进清灰效果,设计出一种线管式双极电袋复合除尘器,并对其增效减阻作用和单极电袋复合除尘器进行了对比研究。在硅微粉中位径1.74μm、过滤风速3 m·min~(-1)、入口粉尘浓度2 500 mg·m~(-3)的实验条件下,双极电袋复合除尘器比单极电袋复合除尘器的粉尘透过率、压力损失分别降低25%、27%以上。为分析双极荷电粉尘的静电凝并增效作用,测定了滤料表面沉积粉尘层的粒度分布,发现单极荷电和双极荷电沉积尘的中位径分别为1.83μm和1.92μm,表明双极荷电粉尘具有较好的静电凝并作用,所形成的较粗团聚颗粒物不易透过滤料,使除尘效率提高。为阐明双极荷电粉尘的减阻作用,采用自然堆积法测出双极荷电粉尘的堆积密度小于单极荷电粉尘,证明粉尘双极荷电后会在滤料表面形成较蓬松的粉尘层,这将有助于降低压力损失、提高清灰效果。     

基于非稳态静电收尘理论的电除尘器运行参数的研究

为了进一步提高电除尘器的收尘效率,满足国家新的烟尘排放标准,依据研究建立的非稳态静电收集理论,提出了电除尘器供电电压及振打周期的优化措施.非稳态静电收尘理论研究与实验研究表明,收尘效率对供电电压存在一最大值,且此最佳供电电压是随极板沉积粉尘层比电阻、粉尘层厚度等动态变化的;振打周期的长短与粉尘层比电阻有关.据此提出的运行参数优化结果表明,对于比电阻不同的粉尘,电除尘器收尘效率最高时对应的供电电压随粉尘层比电阻的增大而降低,对于同一粉尘,最佳供电电压随粉尘层厚度的增长而提高;粉尘层比电阻低于1011Ω·cm时,一般保持极板粉尘层厚度在3～5 mm以内为佳,对于高比电阻粉尘应寻求适宜的清灰方式保障极板处于清洁状态.     

电袋复合除尘器阻力特性研究

利用电袋复合除尘器试验平台,探讨了清洁滤料过滤阻力特性、电场与过滤风速对过滤阻力的影响及本体阻力与测试风量的关系。结果表明:清洁滤料过滤阻力与过滤风速成线性关系,滤料阻力系数为5.39×10~7 m~(-1);无电场作用下,过滤阻力增长率为2.31Pa/min;而65kV电场作用下,过滤阻力增长率仅为0.63Pa/min,主要因为在电场作用下,颗粒层渗透率增大,且荷电粉尘在滤料表面排列疏松,空隙较多,过滤阻力增加慢,可以有效延长喷吹时间,减少喷吹过程对滤袋的冲刷;过滤阻力增长率随过滤风速的增加而增加,过滤风速由0.65m/min增加到0.97m/min,过滤阻力增长率由0.13Pa/min增加到0.63Pa/min;电袋复合除尘器本体阻力(ΔP,Pa)和测试风量(Q,m~3/s)的拟合方程为ΔP=72.15Q~2+25.07Q。     

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.     

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.     

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.     

Biochemical interaction of six op delayed neurotoxicants with several neurotargets

Abstract

Five organophosphorous insecticides: Leptophos, EPN, Cyano‐fenphos, trichloronate and salithion proved to cause irreversible ataxia not only to chicken but also to mice and sheep. TOCP was included as a reference. Cyanofenphos blocked the catecholamine B‐receptor binding activity with ³H‐norepinephrine at a level similar to that of the specific inhibitor propranolol in the mouse heart preparation. In the lamb heart preparation, the B‐receptor was more sensitive to Leptophos, salithion and TOCP than to propranolol. The six compounds and their oxons were screened for their in‐vitro inhibition to monamine oxidase (MAO), acetyl cholinesterase (AChE) and neurotoxic esterase (NTE) in the brain of either mouse, lamb or chicken. It is believed that their AChE inhibition stands for their acute toxicity, while NTE inhibition is responsible for their paralytic ataxia.     

土壤中砷的化学平衡

本文比较详细地综述了砷的化学特性,环境背景值及来源和循环,土壤中砷的三大化学平衡即沉淀溶解平衡,氧化还原平衡,吸附解吸平衡,以及微生物对砷的转化。     

Elemental uptake by edible herbs and lettuce (Latuca sativa)

The total concentration of toxic elements (aluminum, cadmium, chromium and lead) and selected macro and micro elements (iron, manganese, copper and zinc) are reported in six leafy edible vegetation species, namely lettuce, spinach, cabbage, chards and green and red types of Amaranth herbs. Although spinach and chards had greater than 125 mv of iron, both the amaranthus herbs recorded > than 320 μ g g^{? 1} dry weight. In both the spinach and chard species, the Mn and Zn levels were appreciable recording > 225 μ g g^{? 1} and 150 μ g g^{? 1} dry weight, respectively. Aluminum concentrations were (in μ g g^{? 1} dry weight) lettuce (10), cabbage (11), spinach (167), chards (65), amaranthus green (293) and amaranthus red (233). All the micro and macro elements and the toxic elements (Ni, Cr, Cd and Pb) elements analyzed, were below the recommended maximum permitted levels (RMI) in vegetables. Further the elemental uptake and distribution of the nine elements, at three growth stages of the lettuce plant grown on soil bed under controlled conditions are detailed. In the soil, except for iron (16%), greater than 33% of the other cations were in exchangeable form. Generally in the lettuce plant, roots retained much of the iron (> 224 μ g g^{? 1}) and aluminum (> 360 μ g g^{? 1}), while leaves had less than 200 μ g g^{? 1} of iron and 165 μ g g^{? 1} of Al. Although the concentrations of elements marginally decreased with growth, the lettuce leaves had significant amounts of Mn (30 μ g g^{? 1}), Zn (50 μ g g^{? 1}) and Cu (3.6 μ g g^{? 1}). Some presence of lead in leaves (2.0 μ g g^{? 1}) was noticed, but all the toxic and other elements analyzed were well below the RMI values for the vegetables.     

The dissipation of nonlyphenol in stream and pond water under simulated field conditions

Abstract

The dissipation of 1.0 ppm nonylphenol in stream and pond water, incubated in flasks at 16°C under simulated field conditions up to 44 days indicated that the half‐life was 2.5 days if the flasks were open, and 16 days if they were closed. A transformed product was detected in the closed flasks.

Translocation of nonylphenol in water occurred when treated water samples were incubated in the presence of sediment. After 10 days, nonylphenol was detected only in the sediment, but not in water (detection limit = 10 ppb). About 80% of the nonylphenol was degraded in 71 days, but no degradation occurred if the water and the sediment were autoclaved prior to incubation.