Quantitative determination of volatile organic compounds in indoor dust using gas chromatography-UV spectrometry

A novel technique, gas chromatography-UV spectrometry (GC-UV), was used to quantify volatile organic compounds (VOCs) in settled dust from 389 residences in Sweden. The dust samples were thermally desorbed in an inert atmosphere and evaporated compounds were concentrated by solid phase micro extraction and separated by capillary GC. Eluting compounds were then detected, identified, and quantified using a diode array UV spectrophotometer. Altogether, 28 compounds were quantified in each sample; 24 of these were found in more than 50% of the samples. The compounds found in highest concentrations were saturated aldehydes (C5-C10), furfuryl alcohol, 2,6-di-tert-butyl-4-methylphenol (BHT), 2-furaldehyde, and benzaldehyde. Alkenals were also found, notably 2-butenal (crotonaldehyde), 2-methyl-propenal (methacrolein), hexenal, heptenal, octenal, and nonenal. The concentrations of each of the 28 compounds ranged between two to three orders of magnitude, or even more. These results demonstrate the presence of a number of VOCs in indoor dust, and provide, for the first time, a quantitative determination of these compounds in a larger number of dust samples from residents. The findings also illustrate the potential use of GC-UV for analysing volatile compounds in indoor dust, some of which are potential irritants (to the skin, eyes or respiratory system) if present at higher concentrations. The potential use of GC-UV for improving survey and control of the human exposure to particle-bound irritants and other chemicals is inferred.     

Emissions from small-scale energy production using co-combustion of biofuel and the dry fraction of household waste

In sparsely populated rural areas, recycling of household waste might not always be the most environmentally advantageous solution due to the total amount of transport involved. In this study, an alternative approach to recycling has been tested using efficient small-scale biofuel boilers for co-combustion of biofuel and high-energy waste. The dry combustible fraction of source-sorted household waste was mixed with the energy crop reed canary-grass (Phalaris Arundinacea L.), and combusted in both a 5-kW pilot scale reactor and a biofuel boiler with 140-180 kW output capacity, in the form of pellets and briquettes, respectively. The chlorine content of the waste fraction was 0.2%, most of which originated from plastics. The HCl emissions exceeded levels stipulated in new EU-directives, but levels of equal magnitude were also generated from combustion of the pure biofuel. Addition of waste to the biofuel did not give any apparent increase in emissions of organic compounds. Dioxin levels were close to stipulated limits. With further refinement of combustion equipment, small-scale co-combustion systems have the potential to comply with emission regulations.     

Do environmental management programs improve environmental performance trends? a study of standard & poors 500 companies

In this article, environmental management programs of Standard & Poors (S&P) 500 companies were evaluated using a series of industry and size-adjusted environmental trend indicators. The statistical analysis shows that a handful of corporate policy, governance, human resources, auditing, and financial parameters are highly relevant to improving corporate environmental performance. The results have implications for corporate environmental efforts as well as future government policies to foster environmental improvement.     

Organic carbon oxidation induced by large-scale shallow water intrusion into a vertical fracture zone at the Äspö Hard Rock Laboratory (Sweden)

Entrance tunnel construction at the Äspö Hard Rock Laboratory opened a conductive vertical fracture zone at a depth of 70 m on March 13, 1991. Three weeks later a sharp dilution front corresponding to 80% shallow water inflow to the originally saline fracture zone arrived at the entrance tunnel depth. In spite of this large inflow of shallow water, the fracture zone has remained persistently anoxic over a subsequent period. Results from gas sampling and ¹⁴C dating of dissolved organic and inorganic carbon conclusively show that recent organic carbon is being transported into the fracture zone and oxidized to carbon dioxide. These results are important when considering possible changes of redox status in the deep groundwater environment during construction and operation of a repository for spent nuclear fuel. Opening this fracture zone to large-scale surface water inflow adds reducing capacity in the form of organic carbon. This implies that the soil cover may provide important protection against input of dissolved oxygen to fractures being drained during the open phase of the repository.     

Evaluation of solid sorbents for sampling nitroglycerin,ethylene glycol dinitrate and isopropyl nitrate in work-room air

Activated charcoal, Amberlite XAD-2, and Amberlite XAD-7 have been evaluated for the solid sampling of airborne nitroglycerin, ethylene glycol dinitrate and isopropyl nitrate. With the use of diethyl ether for solvent desorption, XAD-2 was found superior for sampling nitroglycerin and ethylene glycol dinitrate. Both XAD-7 and activated charcoal gave high recoveries for isopropyl nitrate; charcoal had a greater capacity than XAD-7 for this compound, however.     

Carbendazim sorption-desorption in Vietnamese soils

Four Vietnamese soils (denoted AG, CT, ST and TG) which differed with respect to pH (pH 2.9-5.4), clay (17-50%) and organic matter (0.3-9.8%) content, were selected for sorption and desorption studies of carbendazim using the batch equilibration technique. Sorption increased with increasing organic carbon (OC) and clay content. Kd values for carbendazim sorption on AG, CT, ST, TG soils at initial concentration of 20 microg/g were 12.5, 127, 8.1 and 9.6 ml/g, respectively. The OC partition coefficients (Koc) for AG, CT, ST and TG were 1140, 1300, 2700 and 960 ml/g, respectively. Carbendazim was strongly sorbed and the binding was less reversible in the acid sulfate soil (CT), than in the other soils. The CT soil had both the highest OC content (9.8%) and the highest clay content (49.8%). The influence of pH on carbendazim sorption was studied in the ST and CT soils. Sorption of carbendazim by the sandy ST soil (OC 0.3%; clay content 26.3%) increased as the pH decreased, while sorption of carbendazim by the CT soil decreased as pH decreased.     

Evaluation of solid sorbents for sampling aliphatic and aromatic nitro compounds in work-room air

Amberlite XAD-2 and XAD-7 porous polymers were evaluated for the solid sampling of aliphatic and aromatic nitro compounds in work-room air. With the use of solvent desorption, XAD-2 gave 80–100% recovery of nitroaromatics, and XAD-7 85–100% recovery of nitroaliphatics. The compounds studied were nitromethane, nitroethane, 2-nitropropane, nitrobenzene, $\text{m}$-dinitrobenzene and 2,4,6-trinitrotoluene. All six compounds gave very poor recoveries from activated charcoal.     

Determination of Mancozeb in air. Occupational exposure during its use in control of potato late blight

A simple method for the determination of occupational exposure to Mancozeb (an ethylenebisdithio-carbamate) was evaluated. This method is based on filter sampling and determination of the manganese content in the samples by means of atomic absorption spectroscopy. The method shows good linearity and accuracy for determinations in the range 0.05 to 2 mg/m³. Exposure during field application of Mancozeb in potato cultivations was studied and was found, during preparation and filling of the spraying liquid, to be 0.22 mg/m³ on average (n=18). The highest individual eight-hour time-weighted average exposure was 0.05 mg/m³.     

Chemical ionisation mass spectra of urea derivatives of diisocyanates

The mass spectrometric behaviour of 9-(N-methylaminomethyl)-anthracene derivatives of diisocyanates and the commercial prepolymer of hexamethylenediisocyanate, N,N′2-tris(6-isocyanatohexyl)imidodicarbonic diamide, was studied. Both positive and negative ion chemical ionisation mass spectra with methane as the reagent gas were investigated and the positive ion spectra were found to be the most informative. They all showed quasimolecular ions, (M+1)⁺, as well as fragments useful for identification purposes.     

Effects of small-scale habitat fragmentation on predator–prey interactions in a temperate sea grass system

During the last decades, fragmentation has become an important issue in ecological research. Habitat fragmentation operates on spatial scales ranging over several magnitudes from patches to landscapes. We focus on small-scale fragmentation effects relevant to animal foraging decision making that could ultimately generate distribution patterns. In a controlled experimental environment, we tested small-scale fragmentation effects in artificial sea grass on the feeding behaviour of juvenile cod (Gadus morhua). Moreover, we examined the influence of fragmentation on the distribution of one of the juvenile cod’s main prey resources, the grass shrimp (Palaemon elegans), in association with three levels of risk provided by cod (no cod, cod chemical cues and actively foraging cod). Time spent by cod within sea grass was lower in fragmented landscapes, but total shrimp consumption was not affected. Shrimp utilised vegetation to a greater extent in fragmented treatments in combination with active predation. We suggest that shrimp choose between sand and vegetation habitats to minimize risk of predation according to cod habitat-specific foraging capacities, while cod aim to maximize prey-dependent foraging rates, generating a habitat-choice game between predator and prey. Moreover, aggregating behaviour in grass shrimp was only found in treatments with active predation. Hence, we argue that both aggregation and vegetation use are anti-predator defence strategies applied by shrimp. We therefore stress the importance of considering small-scale behavioural mechanisms when evaluating consequences from habitat fragmentation on trophic processes in coastal environments.