额济纳河水质污染特征

对额济纳河历年水质监测数据的分析表明 :额济纳河为四级中度污染水体 ,污染有加重趋势 ;主要污染因子是总硬度、悬浮物 ;流域内水土流失及风沙较多是造成污染的主要因素     

高效染料脱色菌的分离鉴定及其脱色特性

从印染废水的处理装置中分离到多株脱色菌，其中一株高效脱色菌经鉴定为腐败希瓦氏菌（Shewanella putrefaciens)。该菌株在合适条件下能有效地去除印染生产上常用的多种染料，在6h内对活性艳红染料的去除率可达到99%-100%，实验还对充氧，温度及共代谢碳源等诸因子对该菌脱色能力的影响进行了研究。     

Metabolic diversity in epibiotic microflora associated with the Pompeii wormsAlvinella pompejana andA. caudata (Polychaetae: Annelida) from deep-sea hydrothermal vents

Specimens of alvinellid polychaetes (Alvinella pompejana Desbruyères and Laubier, 1980 andA. caudata Desbruyères and Laubier, 1986) and their tubes were sampled from deep-sea hydrothermal vents at 13°N from the manned submersible Nautile during the Hydronaut cruise (October to November 1987) on the East Pacific Rise. Samples were subjected to bacterial analysis aboard the mother ship Nadir to detect bacteria involved in the nitrogen and sulphur cycles, in non-specific heterotrophic processes, and displaying resistance to selected heavy metals. Cultures were incubated at different temperatures under atmospheric and in situ (250 atm) pressures. Bacterial growth was observed in enrichment cultures for most metabolic types screened. Heavy-metal-resistant bacteria were also detected in many samples. No filamentous bacterial form was observed in the cultures. The results demonstrate a high metabolic diversity in episymbiotic flora, indicating that the worm (A. pompejana orA. caudata), its tube and its epiflora represent a complex micro-ecosystem.     

Dynamique du phytoplancton et matière organique particulaire dans la zone euphotique de l'Atlantique Equatorial

At two fixed stations in the Equatorial Atlantic Ocean (0°–4° W), the physical, chemical and biological properties of the euphotic layer were determined for 14 d (Station A: 5–18 February, 1979) and 13 d (Station B: 20 October–7 November, 1979), respectively. The stability of the water column allowed comparison of 3 different “systems”: (i) a well-illuminated and nitrate-depleted mixed layer; (ii) a chlorophyll maximum layer (chl a _max) in the thermocline which is poorly illuminated (6.3% of surface irradiance); (iii) a well-illuminated but nitrate-rich (>0.9 μg-at l^-1) mixed layer. In each layer the particulate organic carbon (COP), nitrogen (NOP) and phosphorus (POP) contents were measured and compared with the phytoplankton biomass. In the chlorophyll maximum layer, the phytoplankton biomass contributed significantly to the total particulate organic matter (between 55 and 75%). In the nitrate-depleted mixed layer, the results varied according to whether the regression technique [COP=f(chl a)] was used, or the chl a synthesis during the incubation of the samples. With the former technique, the phytoplankton carbon (C _p) content appeared minimal, because the y intercept, computed using all the data of the water column, was probably overestimated for this layer. POP would be more associated with living protoplasm than with carbon and nitrogen in the three layers. In the chlorophyll a maximum layer it constitutes a valuable detritus-free biomass measurement, since 80% of the POP consist of phytoplankton phosphorus. The assimilation numbers (NA=μg C μg chl a ^-1 h^-1) were high in all three layers, but the highest values were recorded in the nitrate-depleted mixed layer (NA=15 μg C μg chl a ^-1 h^-1). In the chlorophyll maximum layer, light would be a limiting factor during incubation: between 10²⁵ and 8.10²⁴ quanta m^-2 d^-1 NA and light are positively correlated independant of nitrate concentration. The growth rates of phytoplankton (μ) were estimated and compared to the maximum expected growth rate. Our main conclusion was that despite very low biomass and nutrient content, the mixed layer was in a highly dynamic state, as evidenced by high rates of phytoplankton growth and short nutrient turnover times (1 d or less for PO-P₄ in the mixed layer versus 3 d in the thermocline). The presence of nitrate in the water column allows the development of a higher phytoplankton biomass but does not increase growth rate.     

Contribution of the gasoline distribution cycle to volatile organic compound emissions in the metropolitan area of Mexico City

Gasoline distribution in the metropolitan area of Mexico City (MAMC) represents an area of opportunity for the abatement of volatile organic compound (VOC) emissions. The gasoline distribution in this huge urban center encompasses several operations: (1) storage in bulk and distribution plants, (2) transportation to gasoline service stations, (3) unloading at service stations' underground tanks, and (4) gasoline dispensing. In this study, hydrocarbon (HC) emissions resulting from breathing losses in closed reservoirs, leakage, and spillage from the operations just listed were calculated using both field measurements and reported emission factors. The results show that the contribution of volatile HC emissions due to storage, distribution, and sales of gasoline is 6651 t/year, approximately 13 times higher than previously reported values. Tank truck transportation results in 53.9% of the gasoline emissions, and 31.5% of emissions are generated when loading the tank trucks. The high concentration of emissions in the gasoline transportation and loading operations by tank trucks has been ascribed to (1) highly frequent trips from distribution plant to gasoline stations, and vice versa, to cope with excessive gasoline sales per gasoline station; (2) low leakproofness of tank trucks; and (3) poor training of employees. In addition, the contribution to HC evaporative and exhaust emissions from the vehicles of the MAMC was also evaluated.     

Interaction between components of electroplating industry wastes. Influence of the receiving water on the toxicity of the effluent

A copper-cadmium-nickel-zinc mixture was assessed in seven different river waters to study metal toxicity to the ciliate protozoan Colpidium campylum, the interactions occurring between metals, and the influence of the receiving water on toxicity. In the range of concentrations tested, which are representative of electroplating industry wastes, the main part of the toxicity can be attributed to copper and to cadmium-copper synergy. A classification of waters, based on a principal component analysis (PCA), was used to examine the main parameters of the water, which can affect the toxicity of metal mixtures. It appears that the mineralization of the water, more than the total organic carbon (TOC), is an important parameter for the expression of toxicity. A strategy for the estimation of ecotoxicological hazard assessment, based on a simplified factorial experiment is proposed. It enables one to study, in a two-step bioassay, the toxicity of an effluent, the influence of river water on its toxicity, and the effects of contact time and dilution. By applying PCA to data from very different waters, it may be possible to estimate the ecotoxicological risk associated with the discharge of an effluent, on the basis of the chemistry of the receiving water.     

Removal of arsenic(V) from aqueous solutions using iron-oxide-coated modified activated carbon.

Removal of arsenic(V) from aqueous solutions was evaluated with the following three different sorption materials: coal-based activated carbon 12 x 40 (activated carbon), iron(II) oxide (FeO)/activated carbon-H, and iron oxide. The apparent characteristics and physical chemistry performances of these adsorbents were investigated by X-ray diffraction, nitrogen adsorption, and scanning electronic microscope. Also, batch experiments for arsenic removal were performed, and the effects of pH value on arsenic(V) removal were studied. The results suggest that the main phases of the iron oxide surface are magnetite, maghemite, hematite, and goethite; fine and uniform iron oxide particles can cover activated carbon surfaces and affect the surface area or pore structures of activated carbon; adsorption kinetics obey a pseudo-first-order rate equation; and adsorption capacities of adsorbents are affected by the values of pH. The optimum value of pH for iron oxide lies in a narrow range between 4.0 and 5.5, and arsenic(V) removal by FeO/activated carbon-H is ideal and stable in the pH range 3 to 7, while activated carbon has the lowest adsorption capacity in the entire pH range. Also, the adsorption characteristics of FeO/activated carbon-H composites and virgin activated carbon match well the Langmuir adsorption model, while those of iron oxide fit well the Freundlich adsorption model.     

Real-time black carbon personal exposure levels in microenvironments: Home to home on a round-trip,Hanoi–Singapore

Little is known about personal exposure levels of black carbon (BC), a fraction of PM2.5, specifically in the transport microenvironments. In this study, real-time personal exposure to BC recorded by a portable microAeth AE51 was investigated in microenvironments in a round-trip from Hanoi (Vietnam) directly to Singapore. Personal exposure to BC was monitored in microenvironments at residential flat, in various surface modes of transport (taxi, bus, train), at the airports, and on the airplanes. The study found that personal exposure levels of BC in Singapore were higher than those in Hanoi for the same type of microenvironment in general for most of the microenvironments, except for smoking rooms. The highest exposures in each city were in smoking room in Noi Bai International Airport (NIA) and at bus station in Singapore, reached 98,709 ng/m3 and 44,513 ng/m3, respectively; the lowest personal exposure level was in-flight (approximately 250 ng/m3) for both trips. It is also remarkable that personal exposure to BC in indoor microenvironments was higher than outdoor levels.

Implications: Real-time personal exposure to BC was investigated in microenvironments in a round trip from Hanoi (Vietnam) directly to Singapore. BC personal exposure levels in Singapore were higher than those in Hanoi for the same type of microenvironment except for smoking rooms. Personal exposure to BC levels in indoor microenvironments was higher than in outdoor microenvironments. The highest levels of exposure were 98,709 ng/m3 in the smoking room at Noi Bai International Airport (Hanoi) and 44,513 ng/m3 at the bus station in Changi (Singapore). The lowest BC level was in-flight for both trips, at approximately 250 ng/m3.     

Photocatalytic degradation of atrazine by porphyrin and phthalocyanine complexes

This study principally focused on a new kind of photochemical reaction catalyst: porphyrin and phthalocyanine complexes. In a first step, the preparation of the catalysts was optimized. A resin has been chosen to be the support of the complexes. Efficiency of catalytic activity is performed on the degradation of a pesticide: atrazine. The best atrazine degradation occurs with 4.6% of complexes versus substrate. The role of the surface has also been shown to be important. Then, their performances were demonstrated in terms of kinetics and degradation routes, compared to a classical catalyst: titanium dioxide. This study seeks to assess the efficiency of these systems both in a mercury lamp reactor and under solar irradiation which reduces energy costs. The best atrazine degradation half-life found for the complexes is about 200 min with the iron phthalocyanine. These catalysts exhibit particular oxidation activities. Indeed, the degradation routes have been found different between the semi-conductor and the metallic complexes. These complexes are able to cleave the triazinic ring more efficiently than the titanium dioxide.