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Siloxanes have been found widespread usages in our daily lives, but the knowledge on their migration, transformation and toxicity is still limited. Herein we explored the feasibility of using one-sided silica coated paper as filter membrane to capture siloxanes in the outdoor air, followed by direct mass spectrometric analysis. In contrast to mostly utilized fiber membrane, silica coated paper not only exhibited a higher selective sampling efficiency to three siloxanes with structures of H–[Si(CH3)2–O]7-9-NH2 from air, but also possessed a high tolerance to organic solvent during mass spectrometric analysis. Due to the above features, the analysis sensitivity of those siloxanes with silica coated paper has been improved 3.1–134.8 folds in contrast to those with commercial filter membrane. Furthermore, we monitored variation in the levels of those siloxanes for a period of one month, and found that a close association (R2 = 0.7924–0.9559) existed between their contents and climate parameters (e.g., temperature, weather, atmospheric pressure, humidity, wind direction and wind speed) as well as sampling volume. These knowledge provides a facile and effective methodology to both high-efficient sampling siloxanes and environmental assessment of siloxanes according to climate parameters.

Levoglucosan is used as a tracer of biomass burning; however, its determination often requires expensive analytical techniques. Therefore, this study describes the development of an inexpensive and useful method using paper-based analytical devices (PADs) to determine levoglucosan based on colorimetric measurements. The color intensities were correlated with the analytical concentrations and presented linear behavior in the range from 0 to 64.8 μg mL−1. The achieved limits of detection and quantification were 2 and 6 μg mL−1, respectively. The conversion rate of levoglucosan into glucose was 81 ± 8% and the average recovery was 105 ± 9%. Moreover, the method presented selectivity for levoglucosan, showing variation in colorimetric signal intensity lower than 8% in the presence of other saccharides (xylose, glucose, galactose, maltose, mannose, arabinose, and fructose). The accuracy of the method was confirmed by comparison with gas chromatography-mass spectrometry. The proposed method was explored to determine levoglucosan in samples of atmospheric particulate matter collected in Goiania city (Brazil) and the values ranged from 0.08 to 1.10 μg m−3, showing the high impact of the biomass burning to the particulate matter in the region's atmosphere. The method was also used to detect levoglucosan in rainwater samples. Therefore, the use of PADs can simplify fieldwork involving the determination of levoglucosan in atmospheric particulate matter.

The obnoxious odors generated from pulp and paper industries have been the cause of nuisance since the instigation of these industries. The objective of the study was to develop a metal oxide sensor based electronic nose for rapid measurement of odorant concentration and associated odor intensity of major reduced sulfur compounds emitted from different sources of these pulp and paper mills. The gas samples collected from the surroundings of major source points of industry were exposed to sensor array of the electronic nose and the change in voltage was measured and taken to PC through data acquisition cards. The same sets of samples were also tested with gas chromatography. The results of electronic nose and GC-FPD were correlated using response surface methodology to know the odorant concentration. The model fed with unknown industrial samples had more than 95% prediction capability. To determine odor intensity by electronic nose firstly a collective index was generated using SVD based 2-norm method (e-nose index) proportional to the sensors response relative to reference gas, methyl mercaptan. Secondly the e-nose index was associated with human expert evaluations. The training of the electronic nose enabled it to predict odorant concentration found at the industrial site and associated odor intensity in methyl mercaptan equivalent. The overall results of the experiments carried out suggest the potential of electronic nose as a device for on or off line measurement of odorant concentration and odor intensity.

Acidity is a critical characteristic of aerosol particles that impacts many atmospheric chemical reactions. However, the measurement of aerosol acidity remains challenging because of the high ionic strength of atmospheric aerosol particles. In this study, we developed and evaluated a direct method for measuring the pH of atmospheric aerosol samples using pH testing paper. We first examined the color responses of six pH testing papers under various ionic strengths and selected the best performing paper for further testing at higher ionic strength. This paper was then tested under realistic high-ionic-strength conditions created using hygroscopic equilibrium under high and constant relative humidity (RH). A KNO3 saturated solution was used to maintain an RH of 92% in an airtight box. Under these conditions, the hygroscopic constituents in aerosol particles form droplets of aqueous solutions that possess high ionic strength. On the basis of these results, a method for the direct pH measurement of aerosol particle samples was developed. The pH of the atmospheric aerosol samples was measured using this method under high RH to demonstrate its versatility. Our results indicate that this method requires more than approximately 12 μg per spot of fine (PM0.2–2.0 in this study) particles to form a detectable droplet. Compared with previous methods, our direct pH measurement method is simpler, more convenient, and reliable for wide application without excess dilution in practice, and it may be used to obtain important basic information required to study atmospheric aerosols.

On-site measurement of methanethiol (CH 3 SH) was performed for three years on ships and cars near a pulp and paper plant standing on the shore of Lake Baikal in Siberia, Russia, to investigate the behavior and impact of atmospheric CH 3 SH emitted from a point source. Despite its strong odor, there are few reports on atmospheric CH 3 SH, while many investigations have been carried out on dimethyl sulfide (DMS). In this work, CH 3 SH and DMS were measured every 15 min by a recently developed automated instrument based on single column trapping/separation and chemiluminescence measurement. Hydrogen sulfide, sulfur dioxide and ozone were also measured simultaneously by individual instruments. Of these sulfur compounds, CH 3 SH was dominant and its concentration sometimes reached several tens of ppbv. The concentration of CH 3 SH was high at night, because of the lack of photodecomposition and local winds from the mountain to the lake. Such time variation was marked in the summer. The CH 3 SH level decreased significantly downwind, while decreases in concentrations of other compounds such as DMS and SO 2 were relatively small. From these temporal and spatial variations, the behavior of CH 3 SH is described in this paper. The impact of CH 3 SH near the Siberian big sources is discussed with the presented data.

Cooling tower emissions are harmful for several reasons such as air polluting, wetting, icing and solid particle deposition, but mainly due to human health hazards (i.e. Legionella). There are several methods for measuring drift drops. This paper is focussed on the sensitive paper technique, which is suitable in low drift scenarios and real conditions. The lack of an automatic classification method motivated the development of a digital image process algorithm for the Sensitive Paper method. This paper presents a detailed description of this method, in which, drop-like elements are identified by means of the Canny edge detector combined with some morphological operations. Afterwards, the application of a J48 decision tree is proposed as one of the most relevant contributions. This classification method allows us to discern between stains whose origin is a drop and stains whose origin is not a drop. The method is applied to a real case and results are presented in terms of drift and PM10 emissions. This involves the calculation of the main features of the droplet distribution at the cooling tower exit surface in terms of drop size distribution data, cumulative mass distribution curve and characteristic drop diameters. The Log-normal and the Rosin–Rammler distribution functions have been fitted to the experimental data collected in the tests and it can been concluded that the first one is the most suitable for experimental data among the functions tested (whereas the second one is less suitable). Realistic PM10 calculations include the measurement of drift emissions and Total Dissolved Solids as well as the size and number of drops. Results are compared to the method proposed by the U.S. Environmental Protection Agency assessing its overestimation. Drift emissions have found to be 0.0517% of the recirculating water, which is over the Spanish standards limit (0.05%).

The concentration of polycyclic aromatic hydrocarbons (PAHs) in the ambient air from a massive open burning of joss paper was simultaneously measured at an open-burning site (OS) and a downwind site (DS) from 6 to 8 August 2006. A total of 16 major PAHs (particle-bound and gas-phase) concentrations were extracted by the Soxhlet analytical method and analyzed by gas chromatography. The dominant PAHs of the total mass of the organic compound at both the sampling sites were low-molecular-weight species. Further, the results showed that the start burning/end burning-dominant PAH concentration ratios at the OS and DS were 10 and 6.2, respectively. Diagnostic ratios were also used in this study to characterize and identify the PAH emission sources. The results suggest that the characterization of air pollutants emitted from open-burning joss paper lies between furnace-burning joss paper and wood combustion.

The emissions of polycyclic aromatic hydrocarbons (PAHs) were quantified for two joss paper furnaces burning two kinds of joss papers (recycled paper made and virgin bamboo made). A cyclone and a wet scrubber were installed in series on one of the two furnaces. Particulate and gaseous PAHs were collected with a sampling system meeting the criteria of U.S. EPA Modified Method 5. Twenty-one species of PAH were analyzed by GC/MS. Individual PAH emission factors vary from less than 1 mg kg −1 fuel to several tens of mg kg −1 fuel. The total (sum of 21 compounds) and the carcinogenic PAH (benz[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, indeno[1,2,3,-cd]pyrene, dibenz[a,h]anthracene) emission factors were not statistically different for the two furnaces and averaged 71.0 and 3.2 mg kg −1 , respectively. The PAH profiles showed a predominance of naphthalene (58.1%), phenanthrene (11.7%) and fluorene (7.5%). Of the two joss papers examined, bamboo-made joss paper showed less emission in both particulate and gaseous PAHs. For particulate and gaseous PAHs, the removal efficiencies of total PAHs by the air pollution control devices were 42.5% and 11.7%, respectively. PAH emission factors in high airflow conditions were generally lower than those in low airflow condition.

A lifecycle assessment to estimate greenhouse gas emissions in Australia from the paper cycle is summarised. The greenhouse gas emissions from paper in Australia in 1999/2000 were estimated to be 12.1 million tonnes (Mt) of CO2 equivalent. Nearly half of this amount consisted of CH4 emissions from landfilled waste paper. Various waste management options were modelled to investigate the greenhouse impact of a tonne of paper over its whole lifecycle. Options that keep paper out of landfills significantly reduce greenhouse emissions, waste-to-energy recovery being most effective. Recycling is also beneficial, and is of particular interest from a management perspective because it can be controlled by the pulp and paper industry. These findings can be extended to other wood-based and organic wastes.

High ozone levels are regularly reached during summer period in South-European urban areas, calling for careful design of primary pollutants emission reduction strategies. In this perspective the CALGRID modelling system has been applied to Milan metropolitan area, located in the Po Valley, the most industrialised and populated area in Italy. For the first modelling exercise, a simulation domain of 100×100 km2 has been considered and a summer period, characterised by high photochemical activity, has been selected. Hourly emissions have been derived by spatially and temporally disaggregating national inventories data, while standard upper-air and ground-based meteorological data have been used as input to the CALMET pre-processor. A careful analysis of simulation results versus local network monitoring data has revealed some critical points, related to both modelling assumptions and practical data availability. A satisfactory reproduction of daytime ozone behaviour has been, in fact, accomplished, both in urban and suburban sites, while nighttime primary pollutants accumulations and consequent ozone consumption simulated by the model have not found correspondence in the measurements. Nitrogen dioxide has been also successfully modelled, mostly in city surroundings, whereas higher discrepancies have been found in some urban stations. Possible explanations of these facts are discussed in the paper, giving an insight for further work.

Original editorial can be found at: http://www.sciencedirect.com/ Copyright Elsevier [Full text of this paper is not available in the UHRA]