瑞典梅拉伦湖支流中的磷:分析馏分、人为贡献率及生物利用率

关于河流磷(P)浓度以及向瑞典第三大湖梅拉伦湖的磷输送量,现已在12条大支流中进行了为时35年的监测.在15个月时间内,对颗粒磷、悬浮物以及溶解活性磷进行了补充评价.按照水流加权平均数.颗拉磷占64%,溶解非活性磷占23%,溶解活性磷占13%,而且冬节性变化很大.对河流中的"背景"或"基准"磷输送量采用不同方法进行了估算,而人为对磷输送量的贡献呈现出随着时间推移而减少的趋势.对于排了水的耕地和森林覆盖地来说,藻类对颗粒磷的潜应利用率平均约为45%,而污水排放颗粒磷和藻类磷的利用率则较高.支流中的计算生物可利用总磷显示出与粗过滤水上测得的活性磷细等,同时有迹象表明在人为磷贡献率高的时期生物可利用磷的比例要比人为磷贡献率低的时期高.     

Women and community water supply programmes: An analysis from a socio-cultural perspective

Community water supply programmes are seen as instrumental in achieving the goal of ‘safe’ water for all. Women, a principal target group of these programmes, are to be benefited with greater convenience, enhanced socio‐cultural opportunities and better health for themselves and their families, provided through improved water facilities. Water supply programmes largely consist of three essential components, namely: technology, people and institutions. Although such programmes are intended to benefit women members of local communities, scant attention is paid to the impacts of the socio‐cultural context of the community on these programmes. This article explores the influence of social and cultural intricacies on the implementation of community water supply programmes, and assesses their effectiveness. The article offers important lessons for the design and implementation of this type of programme. It concludes that the local socio‐cultural context sets the stage for programme implementation, being a dynamic factor that determines actual access to water sources, more so than mere physical availability, which is often used as a criterion for programme performance. The article stresses the urgent need to integrate socio‐cultural factors as a fourth dimension in designing community water supply programmes, and suggests practical measures for enhancing the effectiveness of such programmes.     

Airborne thermal degradation products of polyurethene coatings in car repair shops

A methodology for workplace air monitoring of aromatic and aliphatic, mono- and polyisocyanates by derivatisation with di-n-butylamine (DBA) is presented. Air sampling was performed using midget impinger flasks containing 10 ml of 0.01 mol l(-1) DBA in toluene and a glass-fibre filter in series after the impinger flask, thereby providing the possibility of collecting and derivatising isocyanates in both the gas and particle phases. Quantification was made by LC-MS, monitoring the molecular ions [MH]+. Air samples taken with this method in car repair shops showed that many different isocyanates are formed during thermal decomposition of polyurethane (PUR) coatings. In addition to isocyanates such as hexamethylene (HDI), isophorone (IPDI), toluene (TDI) and methylenediphenyl diisocyanate (MDI), monoisocyanates such as methyl (MIC), ethyl (EIC), propyl (PIC), butyl (BIC) and phenyl isocyanate (PhI) were found. In many air samples the aliphatic monoisocyanates dominated. During cutting and welding operations, the highest levels of isocyanates were observed. In a single air sample from a welding operation in a car repair shop, the highest concentrations found were: MIC, 290; EIC, 60; PIC, 20; BIC, 9; PhI, 27; HDI, 105; IPDI, 39; MDI, 4; and 2,4-TDI and 2,6-TDI 140 microg m(-3). Monitoring the particle size distribution and concentration during grinding, welding and cutting operations showed that ultrafine particles (< 0.1 microm) were formed at high concentrations. Isocyanates with low volatility were mainly found in the particle phase, but isocyanates with a relatively high volatility such as TDI, were found in both the particle and gas phases.     

Solvent-free sampling with di-n-butylamine for monitoring of isocyanates in air

The solvent-free sampler for airborne isocyanates consisted of a polypropylene tube with an inner wall coated with a glass fibre filter, coupled in series with a 13 mm glass fibre filter. The filters were impregnated with reagent solution containing equimolar amounts of di-n-butylamine (DBA) and acetic acid. Air sampling was performed with an air flow of 0.2 l min(-1). The formed isocyanate-DBA derivatives were determined using liquid chromatography and tandem mass spectrometry. The sampler was investigated in regard to collection principle and extraction of the formed derivatives with good results. The possibility to store the sampler before sampling and to perform long-term sampling was demonstrated. Field extraction of the sampler was not necessary, as there was no difference between immediately extracted samples and stored ones (2 days). In comparative studies, the sampler was evaluated against a reference method, impinger-filter sampling with DBA as reagent. The ratios between the results obtained with the sampler and the reference in a test chamber at a relative humidity (RH) of 45% was in the range of 83-109% for isocyanates formed during thermal decomposition of PUR. At RH 95%, the range was 72-101% with the exception of isocyanic acid. In two field evaluations, the ratios for fast curing 2,4'- and 4,4'-methylene bisphenyl diisocyanate (MDI) was in the range 81-113% and for the 3-ring MDI the range was 54-70%. For the slower curing 1,6-hexamethylene diisocyanate (HDI) and HDI isocyanurate, the ratios were in the range 78-145%. In conclusion, the solvent-free sampler is a convenient alternative in most applications to the more cumbersome impinger-filter sampler.     

Pharmazeutisch aktive Substanzen in kleinen Fließgewässern

Background

Current hydrological research is increasingly focusing on pharmaceutically active compounds (PhACs). Concerning the issue of quality of drinking water, this problem has also become the focus of public interest. However, in spire of the fact that the fate of chemicals in surface waters has been assessed in great detail, the influence of groundwater-exchange is yet only little known.

Goal

This study gives emphasis to the question of how transport and degradation of PhACs interact with the exchange of surface water with groundwater. Special interest is given to alternating groundwater regimes.

Methods

Based on a small stream system in the north of Berlin, Germany, a one-dimensional compartment-model was established using differential mass-balance. The stream which, at its mouth, discharges 0.3 m³ s^?1 is already well investigated and thus provides a good empirical data basis. The processes taken into account by the model were ‘exchange of surface-water with groundwater’, ‘decomposition’ as well as ‘transport’ of PhACs. Calculations were performed using the commonly used analgesic Diclofenac as an example and defining 81 scenarios by different groundwater regimes. Hasse Diagramm Technique was used to compare the scenarios.

Results

All scenarios show a big influence of groundwater-exchange to the fate and concentration of PhACs in surface waters. In the case of the modelled stream system, dilution by groundwater was more responsible for a decrease in concentration than degradation was. Furthermore, on the background of a standard scenario, the loss due to groundwater by 5.4 percent was in the same magnitude as the loss due to decomposition (9.7 percent). A crucial difference between punctual versus linear afflux of groundwater has not been observed.

Discussion

The alteration of discharge resulted in a big influence of the case differentiation between ‘constant velocity’ and ‘constant cross-section’. Furthermore, the model was based on the assumption that groundwater was unloaded with PhACs or diluted very well in comparison to the stream. In contrast, regarding measurements in the catchment, groundwater could even be a diffuse source of the contamination of the stream.

Conclusions

The fate of PhACs in our model is crucially driven by interactions with groundwater. Therefore, assessing the risk emanating from substances like Diclofenac, it is very important to regard their accessibility to decomposition as well as the morphology of the stream-system and its interactions with the groundwater.

Perspectives

In this model, the process of transport from the surface to groundwater back to the surface was dealt with insufficiently; in order to be able to observe fully developed interaction in a further step of modelling, a groundwater-transportmodel should be coupled completely with a surface-water-model.     

A Simple and Flexible Risk Assessment Method in the Work Environment

The existing risk assessment models in the work environment (on the basis of Standard No. BS 8800:1996; British Standards Institution, 1996) contain the need to determine the probability of the occurrence and the severity of consequences of the influence of hazardous factors on the worker. The determination of the probabilities of the influence of hazards (noise, vibration, chemicals, etc.) is complicated.

The authors of this article have developed a simple risk assessment method that does not contain the probabilities. The method is based on a 2-step model that could be enlarged into a 6-step model.

The implementation possibilities of the model are presented. The existing norms in the work environment in Estonia were analysed and the safety level of a wood-processing factory was determined.     

Modeling of Dry Injection Flue Gas Desulfurization

Dry processes for controlling sulfur dioxide emissions by injecting sodium based sorbents in the ductwork ahead of a bag filter are effective and more simple alternatives to conventional FGD processes. This paper presents a fundamental kinetic model of the dry injection process. Experimental data from pilot scale tests are reported. The model is shown to be applicable to the dry injection process. However, further experimental work is recommended to get a better understanding of the reaction mechanisms.     

Exposure to airborne organophosphates originating from hydraulic and turbine oils among aviation technicians and loaders

This study describes the potential for occupational exposure to organophosphates (OPs) originating from turbine and hydraulic oils, among ground personnel within the aviation industry. The OPs tri-n-butyl phosphate (TnBP), dibutyl phenyl phosphate (DBPP), triphenyl phosphate (TPP) and tricresyl phosphate (TCP) have been emphasized due to their use in such oils. Oil aerosol/vapor and total volatile organic compounds (tVOCs) in air were also determined. In total, 228 and 182 OPs and oil aerosol/vapor samples from technician and loader work tasks during work on 42 and 21 aircrafts, respectively, were collected in pairs. In general, the measured exposure levels were below the limit of quantification (LOQ) for 84%/98% (oil aerosol) and 82%/90% (TCP) of the samples collected during technician/loader work tasks. The air concentration ranges for all samples related to technician work were 相似文献   

酸化湖泊水生生物恢复的理论框架构建

在欧洲和北美广大地区,随着大气硫沉降的减少,地表水体酸度正在逐渐降低,但是对水质改善的生态响应过程却依然扑朔迷离.有些湖泊和河流的生物正在恢复,有些水体的生物并没有得到恢复.为理解这些生物响应的差异,有利于酸雨问题的有效管理,我们需要对下面2个问题有清晰的认识:①生物群落恢复所必须经历的生态步骤;②倘若恢复受阻,从哪里着手对恢复进程实施干预,如何干预.本文通过构建一套理论框架来回答上述问题.第一层框架是基于生态学考虑而构建的,通过决策树来反映生态恢复进程中必须经历的若干步骤,步骤之间则通过管理工具或对瓶颈的响应来连接.水质不佳,移生生物供给不足以建群,以及群落水平上对恢复动态变化的阻碍等等都可能成为恢复的瓶颈所在.第二层框架则是基于管理层次来构建的,为了克服瓶颈,框架指明从哪里着手对恢复进程实施干预,为建模来进一步将框架具体化,需要做哪些研究.一旦我们可以用模型来预测酸化水体生态恢复的速率和程度,对硫排放减少带来的效益评价就变得简单起来.而这些模型的构建需要充分认识恢复进程中的生态步骤.本文提出的理论框架将有助于我们朝这个目标迈进.