C3-C14-alkyl nitrates in remote South Atlantic air

Alkyl nitrates with chain lengths up to fourteen carbons have been detected in the remote troposphere of the South Atlantic Ocean. The concentrations of numerous iso- and n-alkyl nitrates in the range of C3-C12 have been measured. Tenax-GC analysis was applied to determine short chain alkyl nitrates (< C6), while the novel detection of long chain iso- and n-alkyl nitrates was achieved with a high volume sampling technique using silica gel. C3-C12-alkyl nitrates show the lowest concentrations in the trade wind region (3.5 pptv). Higher concentrations in the west wind belt (11.1 pptv) reveal the influence of the South American continent as the source for the alkyl nitrates after long range transport. The concentrations of alkyl nitrates increase in proximity to South America. Measurements of long chain alkyl nitrates in rural air near the city of Ulm (Germany) are given for comparison. In addition, pattern analysis of long chain alkyl nitrates reveal this complex mixture of new compounds to be useful as trace indicators to distinguish continental and marine air masses. Despite the lower photochemical formation yields of primary n-alkyl nitrates compared to secondary n-alkyl nitrates, the primary n-alkyl nitrates are relatively increased in marine air. The reason for this finding cannot be explained so far, but the correlation of secondary/primary n-alkyl nitrates shows a significant differentiation of air samples with continental or marine character.     

Predicting change in fish mercury concentrations following reservoir impoundment

Fish mercury concentrations frequently increase after impoundment of a reservoir. Soil flooding releases organic matter and nutrients, providing food to bacterial communities that methylate inorganic mercury. Methylation and bioaccumulation are the primary pathways for mercury accumulation in fish. We investigated if changes in fish mercury concentrations could be predicted from the change in reservoir size. Data for three fish species, northern pike (Esox lucius), walleye (Stizostedion vitreum), and lake whitefish (Coregonus clupeaformis) from reservoirs in northern Manitoba and northern Quebec were used to evaluate four simple models of change in mercury with change in flooded area. For three additional fish species, all primary carnivores, the preferred model consisted of a single exponential enrichment term. This model successfully predicted two cases not used in model development-one with a large change in area and one with a small change in area. Models with good predictive skill can be developed when the underlying dynamics are known.     

Long-term dispersion and availability of metals from submarine mine tailing disposal in a fjord in Arctic Norway

Mining of Cu took place in Kvalsund in the Arctic part of Norway in the 1970s, and mine tailings were discharged to the inner part of the fjord, Repparfjorden. Metal speciation analysis was used to assess the historical dispersion of metals as well as their potential bioavailability from the area of the mine tailing disposal. It was revealed that the dispersion of Ba, Cr, Ni, Pb and Zn from the mine tailings has been limited. Dispersion of Cu to the outer fjord has, however, occurred; the amounts released and dispersed from the mine tailing disposal area quantified to be 2.5–10 t, less than 5% of Cu in the original mine tailings. An estimated 80–390 t of Cu still remains in the disposal area from the surface to a depth of 16 cm. Metal partitioning showed that 56–95% of the Cu is bound in the potential bioavailable fractions (exchangeable, reducible and oxidisable) of the sediments, totalling approximately 70–340 t, with potential for continuous release to the pore water and re-precipitation in over- and underlying sediments. Surface sediments in the deposit area were affected by elevated Cu concentrations just above the probable effect level according to the Norwegian sediment quality criteria, with 50–80% Cu bound in the exchangeable, reducible and oxidisable fractions, potentially available for release to the water column and/or for uptake in benthic organisms.     

Trace analysis of parabens preservatives in drinking water treatment sludge,treated, and mineral water samples

Parabens have been widely used as antimicrobial agents, mainly in food products, pharmaceuticals, and cosmetics. Although they are known as safe preservatives, they also cause some harm to human health, which has been discussed lately. Therefore, the aim of this study was to evaluate the occurrence of nine parabens (including isomers) in mineral and drinking waters, besides in drinking water treatment sludge (DWTS) samples with determination by liquid chromatography tandem mass spectrometry (LC-MS/MS). Both methods solid phase extraction (SPE) and QuEChERS were validated. Calibration curves showed a correlation coefficient of 0.99 for all compounds. LOQ values ranged from 0.04 to 4 μg L^?1 in aqueous matrices and from 5 to 500 ng g^?1 in DWTS. Recoveries between 70 and 115% were reached with RSD below 20% for all compounds in SPE whereas recoveries between 62 and 119% were found with RSD below 20% for almost all compounds in QuEChERS. Matrix effect had low values (<?20%); it was only above 20% for methylparaben in the SPE and for pentylparaben in the QuEChERS. Using a quick and simple extraction procedures with SPE, QuEChERS, and LC-MS/MS analyses, these methods proved to be selective and sensitive. They were successfully applied to real samples (treated water, mineral water, and sludge), and methylparaben was detected at concentration levels below 0.242 μg L^?1 in mineral and treated water samples and 10 ng g^?1 in DWTS samples.     

Determination of the nitrous oxide emission potential of deammonification under anoxic conditions

Various studies have been performed to determine nitrous oxide (N2O) emissions from conventional biological nitrogen removal processes in wastewater treatment like nitrification and denitrification in the main stream. However, with respect to the overall emissions of a wastewater treatment plant, part-stream treatment for high-strength wastewater (e.g., sludge liquor) is also expected to hold a significant emission potential because of high concentrations and extreme boundary conditions. This paper presents results from a laboratory-scale study on nitrous oxide production by biomass from a deammonification process (nitritation + anammox) under anoxic conditions. It was discovered that N2O formation results from incomplete endogenous denitrification rather than anammox and is dependent on substrate availability. Based on direct measurements of the dissolved N2O concentrations in a sequencing batch reactor, the dynamic behavior of N2O production is characterized in more detail. The results show that, during anoxic conditions, the N2O emission potential of deammonification is significantly lower than from conventional denitrification.     

Modelling the global heat balance

A previous model of the global heat balance has been expanded by including the influence of SO₂ pollution, water content of the atmosphere and cloudiness. It was found that the previous results were not changed significantly by this expansion of the model. The conclusions set up uising the previous model were still valid: (1) it is great importance to include the buffer capacity of the sea, including its dependence on pH and the temperature; (2) it is of importance to include natural climatic variations; (3) the dominanting factor is the trend in the consumption of fossil fuel.     

产业与环境：丹麦展望

近20-30年来,很多国家引进了综合性环境保护法律.然而,人们逐渐认识到,在进行具体技术调控的同时,也需要意识上和管理原则上的改变.为帮助各公司在公司层次上减少、评估、监测和控制环境影响,已经开发了各种环境管理技术.本文根据对丹麦公司的一次调查,论述了下列问题:这些技术是如何在工业中采用的?以及发生态度上的变化了吗?     

Engineering,Operation and Maintenance of Electrostatic Precipitators on Open Hearth Furnaces

The photochemical reaction of various olefins and nitrogen dioxide was studied under conditions of controlled temperature, pressure, and humidity in a 200 liter stirred glass reactor. The hydrocarbon concentration in the reactor during four and five hour irradiation periods was monitored with a flame ionization chromatograph. Reaction rate constants, based on three consecutive first order reactions, were calculated for reactor temperatures of 20, 25, 30, and 35 degrees centigrade. Activation energies for the three consecutive reactions were calculated from the Arrhenius equation. Branched and straight chain olefins were studied at initial concentrations of 5.0 to 10.0 parts per million.s