利用空气自动监测车仪器对空气自动监测站仪器进行质量保证及质量控制的可行性分析

通过对辖区内空气自动监测车仪器与4家公司空气自动监测站仪器的比对分析,得出了空气自动监测车仪器与空气自动监测站仪器的PM10、SO2、NO2相对误差分别为:-32.8%、4.4%、-8.7%,仪器之间显现出良好的线性关系,从比对结果来看,利用空气自动监测车对空气自动监测站进行质量保证和质量控制是可行的.     

简易工况法排放检测限值的分析

根据哈尔滨某检测站的工况法排放检测数据,用SPSS数据分析软件对符合DB11／122—2006标准中规定的不同类别车辆的检测数据分别进行统计分析。结果表明,若在哈尔滨地区借鉴该标准,I类车与Ⅲ类车的部分限值需要调整,这为其他地区设定适合的限值提供了参考。     

类水滑石对污泥焚烧飞灰浸出液中磷的纯化

采用Mg-Fe型类水滑石（LDH）吸附剂提纯污泥焚烧飞灰（ISSA）浸出液中的磷,探究了吸附剂煅烧对磷吸附效果的影响及磷吸附和脱附机理.研究发现,在高浓度磷溶液（>1000mg/L）中,未煅烧的类水滑石（LDHu）磷吸附容量高于煅烧后的类水滑石（LDHc）.LDHu具有典型的层状结构,磷的吸附与脱附主要通过磷和金属离子沉淀-溶解、静电吸附-排斥、配位作用和离子交换实现.而LDHc层状结构消失,形成双金属氧化物,不存在明显的阴离子交换作用.经LDHu或LDHc吸附和NaOH溶液脱附后,ISSA浸出液均具有良好的磷纯化效果,磷相对纯度从36%分别上升至77%和69%,磷回收率分别为84%和57%.纯化后的溶液适合制备高值含磷产物.     

A database for integrated assessment of European agricultural systems

A major bottleneck for data-based policy making is that data sources are collected, managed, and distributed by different institutions, residing in different locations, resulting in conceptual and practical problems. The use of dispersed data for agricultural systems research requires the integration of data sources, which means to ensure consistency in data interpretations, units, spatial and temporal scales, to respect legal regulations of privacy, ownership and copyright, and to enable easy dissemination of data. This paper describes the SEAMLESS integrated database on European agricultural systems. It contains data on cropping patterns, production, farm structural data, soil and climate conditions, current agricultural management and policy information. To arrive at one integrated database, a shared ontology was developed according to a collaborative process, which facilitates interdisciplinary research. The paper details this process, which can be re-used in other research projects for integrating data sources.     

Distribution and persistence of carbaryl in some terrestrial and aquatic components of a forest environment

Abstract

An oil‐based formulation of carbaryl (1‐naphthyl N‐methyl‐carbamate) (Sevin‐2‐Oil) was applied twice by a fixed‐wing aircraft at a dosage rate of 280 g of A.I./ha/application to a coniferous forest near Allardville, New Brunswick. The highest concentrations of the chemical in fir foliage, litter and forest soil 1 h after application were respectively 4.20, 1.21 and 0.59 ppm (fresh weight). The residues dissipated rapidly and the DT50 values obtained from the depletion curves were 2.3 d for foliage and 1.5 d for litter and soil samples. Very low levels (<0.1 ppm) of carbaryl persisted in foliage and litter beyond the 10 d sampling period. The maximum residue level found in stream water was 0.314 ppm and more than 50% of it had dissipated within 1 h. Low but detectable levels (0.001 ppm) of the chemical persisted in water until the end of the 10 d sampling period. Sediment samples contained a maximum level of 0.04 ppm, which dissipated below the detection limit within 5 h. Brook trout and slimy sculpins captured in the stream 1 d after the spray contained on average about 0.04 ppm of carbaryl and none of it was found in 3 d postspray samples.     

An overview of the latest development of microencapsulation for agricultural products

Abstract

For the production of controlled‐release agricultural formulations microencapsulation technologies are now the most used. Over the past two decades enormous progress has been made in order to develop the technologies which allow us to produce formulations tailor made to reach the target and fitting our toxicological requirements. This lecture is devoted to the definition of the criteria for selection of an active ingredient for microencapsulation and to a detailed review of the various techniques used today in commerçai microencapsulated formulations.

Resources are increasingly allocated into microencapsulation research & development by many agrochemical companies. Therefore the next 20 years should continue to yield innovative ideas including significant improvement of the physico‐chemical and toxicological properties of the actual formulations on the market. Some of this new ideas are applied by our company in order to modify or improve those properties playing the key role in the intent for targeted activity:

√ Recombination during production or upon storage.

New protective colloides

Dermal toxicity (LD 50) ‐ secondary protective colloides.

√ Release rate parameters.

Modification by the change of mobility of the active ingredient from the core (solvent or fluid type) affecting transit time and therefore LD 50 values.

√ Oral toxicity (LD 50).

Graft copolymers irreversibly adsorbed to the capsule surface.     

Pentachlorotoluene and pentabromotoluene: Results of a subacute and a subchronic toxicity study in the rat

Abstract

Pentachlorotoluene (PCT) and pentabromotoiuene (PBT) are environmental contaminants detected in the Great Lakes ecosystem. In view of the paucity of toxicity data and the potential for human exposure, a subacute (28 day) and a subchronic (91 day) study were conducted in the rat. In the subacute study, groups of 10 male and 10 female rats were fed the diet containing PCT or PBT at 0, 0.5, 5.0, 50 or 500 ppm for 28‐days. In the subchronic study, the group size was increased to 15, the dose levels were 0, 0.05, 0.5, 5.0, 50 and 500 ppm in the diet and the exposure period was 91 days. Growth rate and food consumption were not affected by exposure to either chemical in the subacute and subchronic study. Clinical observations revealed no abnormalities. Decreased hemoglobin was observed in female rats fed 5.0 ppm PCT and higher levels in the subacute (28 day) study. In the same study the hematocrit value and erythrocyte numbers of females fed 5.0 or 500 ppm PCT diets were significantly lower than the control. In both subacute and subchronic studies mild dose‐dependent histopathological changes were observed in the thyroid, liver and kidney of rats fed PCT and PBT diets. In general male rats were more susceptible than females to the treatment of PCT and PBT. Based on these data, it was concluded that the no observable adverse effect level for PCT was 50 ppm in the diet (3.5 mg/kg b.w./day) and that of PBT was 5.0 ppm (0.35 mg/kg b.w./day).