垃圾焚烧飞灰对染料（亚甲基蓝）的吸附性能

以垃圾焚烧飞灰为吸附剂对亚甲基蓝进行了吸附脱色实验。主要探讨了飞灰粒径、用量、温度、pH值和初始浓度等因素对亚甲基蓝吸附的影响，同时分析了吸附上清液中重金属Pb和Cr的浸出毒性。研究结果表明，在25—45℃、pH值2～12、飞灰用量1～5g范围内，经过180min吸附，亚甲基蓝的脱色率都达75％以上，最高可达99．46％。实验还得出，除重金属Pb外，吸附上清液中重金属的浸出量远远低于《危险废物鉴别标准浸出毒性鉴别》的限定值。因此，若能降低重金属Pb的浸出，飞灰将具有应用于处理染料废水的巨大潜力。     

赭石对模拟重金属废水的吸附效果研究

采用模拟重金属废水的正交试验设计，进行赭石对模拟重金属废水的吸附效果研究，探讨pH、赭石加入量和振荡时间等影响因素对吸附效果的影响。结果表明，在一定pH、赭石加入量和振荡时间条件下，赭石对6种重金属（Pb、Cd、Mn、Zn、Cr和Ni）均有较好吸附效果，对Pb、Cd、Mn、Zn和Cr的最大吸附率可达100%，对Ni的吸附率达8963%。处理后废水中重金属达到污水排放标准。各影响因素对Mn、Zn和Cr吸附效率的影响大小表现为：pH＞赭石加入量＞振荡时间，Ni和Cd表现为：赭石加入量＞pH＞振荡时间，Pb表现为：pH＞振荡时间＞赭石加入量。赭石对废水中重金属吸附的最佳条件为赭石加入量40 g/L，pH 10～10.5，振荡时间2 h。     

重金属的生物吸附技术研究

利用生物包括发酵工业的菌丝体废渣或海洋微生物对重金属的吸附作用，来治理重金属造成的污染，其具有原料丰富，成本低，处理效率高等优点，是目前国外研究较多的一种处理重金属污染的方法。本文从生物吸附的概念、机理、吸附剂的性能，以及生物吸附剂的固定化等诸方面进行了综述。同时阐述了生物对重金属吸附技术研究的发展趋势和应用前景。     

生物吸附重金属的研究进展

从生物吸附的概念、吸附重金属的机理、吸附剂的种类以及生物细胞的固定化、生物吸附工艺过程等方面进行了综述，同时阐述了生物吸附重金属的技术研究进展和应用前景展望。     

麦饭石对重金属离子的吸附作用研究

研究了麦饭石对重金属离子，如Ｐｂ＾２＋、Ｃｕ＾２＋，Ｚｎ＾２＋，Ｃｄ＾２＋的吸附作用，实验结果表明，麦饭石对重金属离子具有较强的吸附性能，ｐＨ是影响吸附的主要因素，探讨了麦饭石吸附作用机理，认为离子交换和表面络合反应是主要的吸附形式。并结合对实际重金属废水的吸附净化作用讨论麦饭石在废水处理方面应用的可行性。     

非固定化和固定化啤酒酵母对Cd2+和Cu2+的吸附特性研究

对比了不同吸附剂对重金属的吸附效果，同时研究了啤酒酵母的固定化方法、菌体用量对吸附效果的影响、非固定化和固定化啤酒酵母吸附热力学特性。研究结果表明，非固定化死啤酒酵母对Cd²⁺的单位菌体吸附量是常用吸附剂活性炭的3倍；由1∶3的海藻酸钠与碱处理啤酒酵母（w/w）制得的固定化颗粒吸附效果最好；菌体用量的增加会降低单位菌体对重金属的吸附量；啤酒酵母对重金属的吸附位点有限，Cd²⁺的实际最大吸附量为13.95 mg/g，Cu²⁺为7.67 mg/     

北运河表层沉积物对重金属Cu、Pb、Zn的吸附

首先分析了北运河6个采样点表层沉积物中重金属含量及相关基本特征。通过实验室模拟实验,利用分配系数Kd评价沉积物对重金属Cu、Pb、Zn的吸附特性,进一步考察了水体pH变化和有机质对重金属在北运河沉积物上吸附的影响。结果表明,沉积物中重金属的含量顺序为Zn>Cu>Pb,去除有机质后,沉积物对重金属的吸附能力显著降低,但各采样点中的重金属含量,沉积物对重金属吸附能力,以及沉积物中的有机质含量并没有明显相关性,这可能是因为不同采样点中有机质种类与结构不同导致的。总之,北运河沉积物对Pb有很强的吸附能力,其次是Cu和Zn,而且,Cu、Zn、Pb的吸附量随着pH的升高逐渐增大,水体pH值对于Zn的吸附影响更大。     

半焦吸附养殖废水中的重金属

采用生物质半焦作为吸附剂处理养殖废水中的重金属,并对半焦吸附重金属的吸附容量及吸附效率进行了分析和评估。实验结果表明,生物质半焦对养殖废水中Cu、Zn、Pb和Cd 4种重金属具有较好的吸附效果,吸附容量分别为22.4、19.03、17.30和16.94 mg/g,且吸附率均达到70%以上,氮磷的影响吸附不超过30%。重金属离子在半焦表面上的吸附过程符合Langmuir等温吸附模型,且主要为单分子层表面吸附。由此生物质半焦作为廉价高效的吸附剂处理养殖废水中重金属技术上可行,为养殖废水中重金属吸附研究及生物质半焦资源化利用提供新途径。     

重金属与土壤微生物的相互作用及污染土壤修复

阐述了微生物与重金属间的相互作用，指出土壤重金属污染影响微生物活性、生物量，且重金属对微生物具有一定的生态毒性。可通过微生物的氧化-还原作用、生物吸附富集和溶解作用，达到修复重金属污染土壤的目的。     

玉米芯对废水重金属的吸附机制及影响因素

分析了玉米芯对重金属的吸附机理及影响吸附量的因素，并对发展动向作了探讨。     

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.     

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.     

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.     

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.