几种室内植物去除低分子羰基化合物

为了寻求治理室内挥发性有机污染物的措施,以豆瓣绿、鹅掌柴、富贵竹和袖珍椰子等4种常见室内植物为供试材料,采用五氟苯肼/气相色谱/质谱法(PFPH/GC/MSD)分析方法和动态熏气法开展了相关植物去除4种羰基化合物(乙醛、丙酮、丙醛和丁醛)的实验研究.结果表明,在有光照(3 000 lx)下,豆瓣绿、鹅掌柴、富贵竹和袖珍椰子4种植物对污染物的去除速率(μmol/(m2·h))范围分别为:0.24(丁醛)～1.36(丙酮)、0.25(丁醛)～0.69(乙醛)、0.07(丁醛)～0.30(乙醛)及0.57(丙醛)～0.75(乙醛),而在无光照下,相应的植物去除速率(μmol/(m2·h))分别为:0.07(丁醛)～0.27(丙酮)、0.09(丁醛)～0.29(乙醛)、0.02(丁醛)～0.22(乙醛)、0.13(乙醛)～0.45(丙酮),通过对比可以看出4种植物对C2～C4羰基化合物在光照下的去除效果明显优于在无光照的情况下.此外,4种供试植物对4种羰基化合物总的去除速率由大到小依次为:豆瓣绿(169.26μg/(m2 · h))＞袖珍椰子(149.23 μg/(m2 h))＞鹅掌柴(94.44 μg/(m2·h))＞富贵竹(29.85 μg/(m2·h)).     

利用废旧锌锰电池制备光催化剂净化甲苯

针对废旧锌锰电池回收利用难,以及光催化剂 TiO2活性低的问题,以废旧锌锰电池和商业二氧化钛为原料,通过球磨法制备了新型复合光催化剂.在紫外光灯照射下,进行了废旧锌锰电池复合改性TiO2对甲苯的光催化氧化实验,并重点探究空速、光照强度、相对湿度和氧气体积分数等关键实验条件对甲苯净化效率的影响.结果表明,改性后的催化剂对甲苯的净化能力大幅提高;当TiO2与废电池芯粉的质量比为2:1时,催化剂的催化效果最好,甲苯的净化效率提高了近45％;空速越大,催化剂对甲苯的净化效率越低;净化效率随光照强度的增加呈现先增加后保持不变的规律;催化剂在相对湿度为30％的条件下具有最佳的催化活性,氧气体积分数为15％时为净化效率达到最大.本研究结果可为废旧锌锰电池的回收利用提供新的思路.     

空气净化器检测用环境试验舱研制及性能评价

研制一种大型环境试验舱,该舱整体构造主要由内舱、外舱、空气净化系统、污染源发生装置和空气采样系统组成。其中,内舱为测试舱主体部分,体积为30 m3。对舱的性能进行评价测试,结果表明:温度和相对湿度的偏差分别为δT≤2.5℃和δRH≤5%;环境舱内外压差在0～5 Pa时,舱体泄漏量为0.03～1.02 m3/h;清洗后,舱内单项污染物本底浓度小于20μg/m3,总挥发性有机物(TVOC)小于90μg/m3;以质量分数为37%的甲醛溶液作代表性污染物,4种投放量下回收率分别为86.6%、83.4%、82.9%和81.5%;舱内温度为21℃,相对湿度为40%时,甲醛、苯、甲苯等3种污染物自衰减分别为6.7%、8.9%和4.7%。实验结果表明该试验舱应用性能良好,可用于检测空气净化器性能及净化效率。     

内、外循环空气净化系统理论模型构建与性能对比分析

室内空气污染对人类健康的影响日益受到关注,目前空气净化系统作为室内空气污染最有效的控制方式,逐渐受到人们的青睐。针对市场上常见的空气净化器和新风净化机这2种空气净化系统,为探究2种系统净化方式的异同,分别构建了内循环、外循环净化理论模型,实际实验验证模型具有正确性。应用模型对影响两系统净化效果的因素进行分析,结果表明,相同条件下,空气净化器对PM_(2.5)去除效率高于新风净化机,且均随着风量、一次通过净化效率、时间的增大而升高,随着房间体积的增大而降低,新风净化机存在最佳建筑物换气次数。室外PM_(2.5)浓度不影响2种空气净化系统对PM_(2.5)的去除率,但随着室外浓度增大,室内PM_(2.5)剩余浓度升高。     

室内空气总挥发性有机物净化实验装置设计及应用

为了探究进气流量和相对湿度对活性炭吸附法和光催化转化法动态净化室内空气中总挥发性有机物(TVOC)的影响,设计了一套包含活性炭吸附器和光催化反应器的多功能空气动态净化实验装置,并利用该装置进行了室内空气净化实验。通过设置不同进气条件(进气流量和相对湿度)对室内空气进行净化实验,采用气相色谱仪对样品TVOC浓度进行检测,并与未经净化处理的空气样品进行对比,计算TVOC去除率。结果表明:该实验装置能够实现连续进气且能对进气流量和相对湿度进行精准调节;随着进气流量增大,活性炭和光催化对TVOC去除率减小;随着进气相对湿度增大,活性炭对TVOC去除率减小,光催化对TVOC的去除率呈现先增大后减小的趋势。以上实验结果为气候舱空气净化系统、家用空气净化器及室内新风过滤系统等动态空气净化系统的设计提供了参考。     

环境测试舱自吸附甲醛重释放规律与影响因素研究

广泛用于板材污染物释放量测试、空气净化产品净化效果测试等实验中的环境测试舱,往往由于其内壁黏附性杂质而对目标测试物产生不可忽视的自吸附作用,自吸附污染物将作为二次释放源出现重释放,研究目标测试物的自吸附消耗量及重释放规律,探索有效控制措施,有利于对环境测试舱实验应用及室内污染控制提出指导性实际意义。分别选取0.2%甲醛溶液、大芯板作为同一自制玻璃环境测试舱2期实验(I期、Ⅱ期)的不同甲醛释放源,通过近90 d追踪测试,经不同释放源、不同控制条件下舱内壁自吸附甲醛的多次重释放实验,结合非线性拟合分析方法,总结出舱内壁自吸附甲醛重释放甲醛浓度变化符合一阶递增指数函数:y=A1×exp(-x/t1)+y0,(A1<0、t1>0)。曲线参数y0值可用于评价实验条件下测试舱内自吸附甲醛残余量;y0值与环境舱舱体材质、环境温湿度、舱外甲醛浓度及空气交换手段有关,而与释放源及其释放平衡浓度高低无明显关系。大开舱门短时间抽气式空气交换对舱内自吸附甲醛残余有适度清除效果,使y0值降低,同时有利于再次平衡状态的快速建立;而长时间的无动力空气交换,或者自来水洗及去离子水洗等处理手段对舱内壁自吸附甲醛残余无明显清除作用。     

电解铝烟尘渣处理方法的探讨

关于电解铝烟气净化工程,提出了某些改进:净化工程的含氟烟灰加石灰水处理,按分子比CaO/Na_2O=0.9～1.1、灰/水=10～3揽拌1小时,可溶性氟盐转化为不溶性的CaF_2,含20～25％CaF_2的残渣可用作矿化剂;含10～30g/LNa_2O、5～20g/LAl_2O_3的浸出液返回烟气净化流程。另外还提出用含氟或含碱的废水化灰,以补充烟气蒸发的水。     

不同改性方式对竹炭净化气态氮氧化物效果的影响

为了研究不同表面改性方法对竹炭空气净化效果的影响,测定了化学药剂活化、超声处理、微波处理后的改性竹炭对低浓度氮氧化物的净化效果。结果表明:活化剂浸渍后的竹炭,对氮氧化物净化效率降低,净化速度减慢;微波功率越大、辐照时间越长,改性后竹炭对氮氧化物处理效率越大,但辐照时间达到一定程度后,竹炭对氮氧化物的处理效率增大变得缓慢;超声处理后的竹炭对NO的处理效率比改性前有明显提高。BET测试结果表明,竹炭产品用微波和超声处理后,平均孔径、微孔表面积和比表面积均比活化前增大;而经过活化剂浸渍后,微孔面积和比表面积都显著下降。因此建议采用微波及超声方式对竹炭进行活化。     

电凝并式空气净化单元对颗粒物和甲醛净化效果的实验

研究一种新型电凝并式空气净化单元对室内空气中颗粒物和甲醛的净化效果.实验结果表明,高压高频(HV-HF)电凝并装置能促使小粒子相互凝并为较大的电中性的粒子团,这些具有较高比表面积的电中性粒子团进入室内空间,能继续粘附空气中及物体表面上的颗粒,形成更大的粒子团,从而易于被净化单元中的中效过滤器捕集,而且该净化单元对于大粒子(粒径＞0.7μm)浓度较高的场所净化效果更加明显.另外,室内空气中吸附在颗粒物表面的甲醛也随之被高效去除.该净化单元的投入使用,起到了提高过滤效率、去除气溶胶小粒子、降低能耗、进一步改善室内空气品质等多重功效.     

生物膜填料塔净化模拟烟气和电厂烟气中SO2和NOx的对比实验

对生物膜填料塔对模拟烟气和电厂烟气的净化效果进行了实验研究。实验对比分析了在相同的实验条件下生物膜填料塔对不同烟气中SO2和NOx的净化效率。实验结果表明,在循环液温度在24～35℃、空床停留时间（EBRT）为60s、喷淋量为8～10L／h、脱硫塔的pH为0．8～1．5、脱氮塔的pH为7．5～8．0的条件下,生物膜填料塔对模拟烟气和电厂烟气中SO2的净化效率都很高,但模拟烟气条件下的总脱氮率的平均值为80％,而在电厂烟气条件下只有35％。经分析认为,脱氮率产生差异的主要原因是电厂烟气中杂质的影响,以及烟气中氧气含量的不同,同时因为生长条件不同从而驯化出的微生物群体组成也不同。     

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.     

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.     

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.     

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 and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

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.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

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.     

Knowledge transfer initiative between molecular biologists and environmental researchers and regulators

A Natural Environment Research Council (NERC) funded Knowledge Transfer (KT) workshop was held in the United Kingdom (UK) to identify the needs and opportunities in the application of molecular biology and ‘omics’ techniques to environmental monitoring and risk assessment. Attendees highlighted a lack of effective communication between end-users and researchers as well as difficulties with data interpretation as reasons behind the slow uptake of molecular biology and omics techniques. A number of promising areas in which new techniques could be implemented at a practical level in the very near future were identified, thereby raising the profile of these recent technologies and providing vital proof of concept work. Molecular taxonomy, bacterial source tracking and pre-screening of chemicals for potential toxicities were all viewed as areas in which omics and molecular techniques could have immediate value, with the aim of reducing cost, increasing efficiency and providing more comprehensive data of improved quality.     

Sorption and predicted mobility of herbicides in Baltic soils

This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine～ amitrole～ simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log K_ow) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.