Atmospheric mineral particles collected at Qira in the Taklamakan Desert, China

Aerosol particles were collected in the situation of the widespread dust suspension on 21 February 1991 at Qira in the southern edge of the Taklamakan Desert, western China. The collected particles were examined by a transmission electron microscope equipped with an energy-dispersive X-ray (EDX) analyzer in order to obtain the size and elemental composition of individual mineral particles.On the basis of EDX analyses for 386 particles, mineral particles were present in high number fractions (>99%) of particles in the radius range of 0.1–4 μm. Particles mainly composed of silicates comprised 76% of mineral particles. “Ca-rich” particles were detected in 7% of all the particles. Ca in the particles would be present not only as CaCO₃ but also as an internal mixture of CaCO₃ and CaSO₄. Particles containing halite (NaCl) were detected in number proportions of about 10% and were mainly present in the radius range of 0.5 μm. Some halite particles would be modified by chemical reactions with sulfuric acid.     

Reactivity between PbSO4 and CaCO3 particles relevant to the modification of mineral particles and chemical forms of Pb in particles sampled at two remote sites during an Asian dust event

During the transboundary transport of anthropogenic heavy metals by mineral particles providing reaction sites, the divalent metal salt PbSO₄ can be converted to PbCO₃ in the presence of water. We carried out laboratory experiments to study the transformation process under various conditions by incorporating test particles comprising CaCO₃ of a particulate mineral component, PbSO₄, and NaCl. After the immersion of PbSO₄ particles in contact with CaCO₃ particles in a water droplet, the conversion of PbSO₄ into PbCO₃ was confirmed by the change in morphology of the original particles to stick or needle form; the percentages of the chemical forms relative to the total Pb were determined by X-ray absorption near edge structure (XANES) analysis. Approximately 60–80% of PbSO₄ was converted to PbCO₃ after 24 h. A small amount of stick particles was detected when NaCl particles attached to PbSO₄/CaCO₃ particles were exposed to air with a relative humidity (RH) of 80–90% for 24 h. XANES measurements of the samples revealed that the molar percentage of PbCO₃ relative to the total Pb content was 4%.Field experiments were also conducted to determine the chemical forms of the Pb particles during the Kosa (Asian dust storm) event. Samples were collected from two remote sites in Japan and Korea. The mass size distribution of Pb aerosols collected in Japan was bimodal with two peaks in the coarse mode; the enrichment factor of Pb suggested that its source was anthropogenic. Pb L3 edge XANES measurements of both samples indicated that they had similar shapes. These measurements also indicated that the major Pb components for the samples collected in Japan were PbO, PbSO₄ PbCl₂, and PbCO₃, with molar percentages of 44%, 30%, 21%, and 5%, respectively. No significant differences were found between the component ratios of the samples collected in Japan and Korea, suggesting that definite transformation did not occur during the transport of the Kosa particles from Korea to Japan. On the basis of these observations, we postulate that the transformation process either occurred mainly before the particles arrived at Korea or did not take place after the particles left continental Asia.     

矿物油淬火剂的环保问题探讨

矿物油碎火剂的污染问题已越来越引起人们的关注，特别是最近调查表明矿物油是地下水的主要污染源，对矿物油碎火剂进行环保治理的要求更是愈加迫切，首先列出了矿物油碎火剂的环境危害，然后对减少和消除矿物的污染，提出了五种可能的解决办法，延长使用寿命，再生处理，矿物碎火油配方的环保改进，开发新的碎火油和使用水基碎火剂等。     

Characteristics of Road Dust from Different Sampling Sites in Northern Taiwan

Abstract

Road dust contributes a large percentage of the atmosphere’s suspended particles in Taiwan. Three road dust samples were collected from downtown, electrical park, and freeway tunnel areas. A mechanical sieve separated the road dust in the initial stage. Particles >100 μm were 75%, 70%, and 60% (wt/wt), respectively, of the samples. Those particles <37 μm were resuspended in another mixing chamber and then collected by a Moudi particle sampler. The largest mass fraction of resuspended road dust was in the range of 1–10 μm. Ultrafine particles (<1 μm) composed 33.7, 17, and 7.4% of the particle samples (downtown, electrical park, and freeway tunnel, respectively). The road dust compositions were analyzed by inductively coupled plasma (ICP)-atomic emissions spectroscopy and ICP-mass spectrometry. The highest concentration fraction contained more aluminum (Al), iron (Fe), calcium (Ca), and potassium than other elements in the road dust particle samples. Additionally, the sulfur (S) content in the road dust from the electrical park and freeway tunnel areas was 2.1 and 3.4 times the downtown area sample, respectively. The sulfur originated from the vehicle and boiler oil combustion and industrial manufacturing processes. Furthermore, zinc (Zn) concentration in the tunnel dust was 2.6 times that of the downtown and electrical park samples, which can be attributed to vehicle tire wear and tear. Resuspended road dusts (<10 μm) from the downtown and freeway tunnel areas were principally 2.5–10 μm Al, barium (Ba), Ca, copper (Cu), Fe, magnesium (Mg), sodium (Na), antimony (Sb), and Zn, whereas arsenic (As), chromium (Cr), and nickel (Ni) were predominant in the ultrafine particle samples (<1 μm). Al, Ba, and Ca are the typical soil elements in coarse particles; and As, and Cr and Ni are the typical fingerprint of oil combustion and vehicle engine abrasion in ultrafine particles. There was a special characteristic of resuspension road dust at electrical park, that is, many elements, including As, Ba, Ca, cadmium, Cr, Cu, Fe, manganese (Mn), Ni, lead (Pb), S, vanadium (V), and Zn, were major in ultrafine particles. These elements should be attributed to the special manufacturing processes of electric products.     

电石炉气热能利用及除尘技术

介绍了将电石炉气直接引入余热锅炉燃烧及除尘技术,该技术在生产中显示了优越的工艺性能,是一种投资省、见效快、安全、经济、节能的可物的技术。     

Dust build-up on surfaces in the indoor environment

The concentration and the composition of dust in the indoor environment has been associated with reported symptoms of the sick building syndrome. Levels of airborne concentrations of dust particles are well known. However, the relation to dust on surfaces for office environments are not well described. In this study, 662 measurements were performed of surface dust concentrations on hard surfaces in 19 buildings within Harvard University based on a sticking gelatine foil method. The measure is the dust covered area of the surface as a percentage. In three offices, the build-up of dust on surfaces was measured for a period of five days. Close to these surfaces the airborne PM_2.5 and PM₁₀ particle mass concentrations were measured simultanously. A significant correlation between the dust build-up and the difference between the PM₁₀ and the PM_2.5 was established. The particle size distribution was measured by means of an Aerodynamic Particle Sizer. The mean dust build-up normalized with the measured PM₁₀ was approximately four times higher than the equivalent calculated by a deposition model. This may in part be due to the effect of preferred orientation when particles settle to a surface. Different data for dust on surfaces and airborne particles in offices were compared. The levels of airborne particles in offices in Europe seem to be higher than the levels in the US.     

Comparison of fine particles and the relationship between particle variations and meteorology at an urban site and a remote site in the Eastern United States

This study compared the variations in the mass of certain particles at an urban site, Washington, DC, and at a remote site, Shenandoah National Park, VA, in the eastern United States. Seven years (1991-1997) of Interagency Monitoring of Protected Visual Environments (IMPROVE) fine particulate matter (PM2.5), PM10, coarse fraction, SO4(2-), and total sulfur data were used for this study together with available meteorology/climatology data. Various statistical modeling and analysis procedures, including time series analysis, factor analysis, and regression modeling, were employed. Time series of the constituents were divided into four terms: the long-term mean, the intraannual perturbation, the interannual perturbation, and the synoptic perturbation. PM2.5 at the two sites made up approximately 72% of the total mass for PM10, and the coarse fraction made up the remaining 28%, on average. Thirty-one percent of the PM2.5 at the DC site and 42% at the Shenandoah site was SO4(2-), based on average data for the entire period. At the DC site, the two main contributors to the constituent mass were the long-term mean and the synoptic perturbation terms, and at the Shenandoah site, they were the long-term mean and the intra-annual perturbation terms. This suggested that the constituent mass at the two sites was affected by very different processes. The terms that provided the principal contribution to the constituent mass at the two sites were studied in detail. At the DC site, dew point trends, a climate variable, were the primary driver of the 7-year trends for PM2.5, PM10, the coarse fraction, and total sulfur, and SO2 emission trends were the primary driver of the trends for SO4(2-). SO2 emission trends influenced the trends for PM2.5 and total sulfur, appearing as the second term in the model, but only parameters dealing with climate trends had significant effects on the trends for PM10 and the coarse fraction. At the Shenandoah site, only parameters dealing with climate trends affected long-term particle trends.     

Seasonal variations of monoterpene emissions from Pinus densiflora in East Asia

The emission rates and compositions of monoterpene from Pinus densiflora were investigated in the Gumsung (GM) and Worak (WM) mountains. The standard emission rates (ERs: ERs is the monoterpene emission rate at standard temperature, 30 degrees C) from P. densiflora ranged from 0.817 to 1.704 (mugC/gdw-h). The ERs and beta-values of total monoterpene were measured at the two study sites (GM and WM). In the spring and summer, the ERs were the highest, while relatively low values (<0.058mugC/gdw-h) were measured in the autumn and winter. In GM and WM sites the beta-value obtained for the different seasons ranged from 0.047 to 0.179, with an average of 0.09. The major monoterpene compounds from P. densiflora were alpha-pinene, myrcene, beta-phellandrene, d-limonene and alpha-terpinene. The fractional compositions of individual monoterpene compounds were significantly different between the two test sites in the summer and winter. The ERs of the older group (31-40 years) were higher than those in the younger group (21-30 years). However, the monoterpene compositions were similar between the two age groups.     

Size distribution of particles emitted from grass fires in the Northern Territory,Australia

This study investigated particle size distributions from the burning of several grass species, under controlled laboratory conditions, and also in the field, conducted during the dry season in the Northern Territory, Australia. The laboratory study simulated conditions such as burning phases and burning rate, and particle diameter differed depending on the burning conditions. Under fast burning conditions, smaller particles were produced with a diameter in the range of 30–60 nm, while larger particles, with a diameter between 60 and 210 nm, were produced during slow burning. The airborne field measurements of biomass particles found that under the boundary layer most of the early dry season (EDS) particles came from fresh smokes with a count median diameter (CMD) of 83±13 nm, and most of the late dry season (LDS) particles came from aged smokes with a CMD of 127±6 nm. Vertical profiles of CMD showed that smaller particles were found higher within the atmosphere. These measurements provide insight into the scientific understanding of the properties of biomass burning particles in the Northern Territory, Australia.     

选矿技术在城市固体废弃物资源化中的应用

选矿技术作为一种成熟的矿物分离技术已广泛应用于城市固体废弃物资源化领域 ,促进了环境的保护和资源的综合回收 ;同时也开辟了选矿技术新的应用领域。结合实例介绍国内外常用的各种城市固体废弃物的分选工艺 ,指出选矿技术的运用对固体废弃物的资源化有着重要的实际意义     

Seasonal variations in VOC emission rates from gorse (Ulex europaeus)

Seasonal variations of biogenic volatile organic compound (VOC) emission rates and standardised emission factors from gorse (Ulex europaeus) have been measured at two sites in the United Kingdom, from October 1994 to September 1995, within temperature and PAR conditions ranging from 3 to 34°C and 10–1300 μmol m⁻² s⁻¹, respectively. Isoprene was the dominant emitted compound with a relative composition fluctuating from 7% of the total VOC (winter) to 97% (late summer). The monoterpenes α-pinene, camphene, sabinene, β-pinene, myrcene, limonene, trans-ocimene and γ-terpinene were also emitted, with α-pinene being the dominant monoterpene during most the year. Trans-ocimene represented 33–66% of the total monoterpene during the hottest months from June to September. VOC emissions were found to be accurately predicted using existing algorithms. Standard (normalised) emission factors of VOCs from gorse were calculated using experimental parameters measured during the experiment and found to fluctuate with season, from 13.3±2.1 to 0.1±0.1 μg C (g dwt)⁻¹ h⁻¹ in August 1995 and January 1995, respectively, for isoprene, and from 2.5±0.2 to 0.4±0.2 μg C (g dwt)⁻¹ h⁻¹ in July and November 1995, respectively, for total monoterpenes. No simple clear relation was found to allow prediction of these seasonal variations with respect to temperature and light intensity. The effects of using inappropriate algorithms to derive VOC fluxes from gorse were assessed for isoprene and monoterpenes. Although on an annual basis the discrepancies are not significant, monthly estimation of isoprene were found to be overestimated by more than a factor of 50 during wintertime when the seasonality of emission factors is not considered.     

Indoor fine particles: the role of terpene emissions from consumer products

Consumer products can emit significant quantities of terpenes, which can react with ozone (O3). Resulting byproducts include compounds with low vapor pressures that contribute to the growth of secondary organic aerosols (SOAs). The focus of this study was to evaluate the potential for SOA growth, in the presence of O3, following the use of a lime-scented liquid air freshener, a pine-scented solid air freshener, a lemon-scented general-purpose cleaner, a wood floor cleaner, and a perfume. Two chamber experiments were performed for each of these five terpene-containing agents, one at an elevated O3 concentration and-the other at a lower O3 concentration. Particle number and mass concentrations increased and O3 concentrations decreased during each experiment. Experiments with terpene-based air fresheners produced the highest increases in particle number and mass concentrations. The results of this study clearly demonstrate that homogeneous reactions between O3 and terpenes from various consumer products can lead to increases in fine particle mass concentrations when these products are used indoors. Particle increases can occur during periods of elevated outdoor O3 concentrations or indoor O3 generation, coupled with elevated terpene releases. Human exposure to fine particles can be reduced by minimizing indoor terpene concentrations or O3 concentrations.     

Unavailability of polynuclear aromatic hydrocarbons from coal particles to the eastern oyster

The accumulation by oysters of polycyclic aromatic hydrocarbons (PAH) from coal dust entering the estuarine environment has been postulated in the vicinity of coal transfer operations. Oysters Crassostrea virginica were exposed to coal dust plus 15 day leachate at concentrations of 10 mg litre(-1) and 1 mg litre(-1) coal dust for 28 days in a flow-through test system. Potential effects of the exposures were measured by comparing the uptake of PAH and the growth of the exposed animals versus control groups. Oysters sampled at 7, 14 and 28 days did not exhibit an increase in PAH body burden over control animals provided the guts were first purged of particulates. Even at the high test concentrations (10 mg litre(-1)), no effect of the exposure on shell growth was observed.     

Pollution of the roadside environment by dust particles from road surface repairs

The purpose of the study is to investigate the practical aspects of environmental pollution near motorways by dust particles formed during repair works and to identify specific ways to improve the overall environmental situation near highways and reduce the level of pollution during road maintenance. The leading approach is a systematic analysis of the problems of environmental pollution by dust emissions in general. The study results reflect the entire volume of research efforts made to determine the optimal composition of the concrete mixture for road repairs, which allows reducing the emission of dust particles into the surrounding roadside environment and improves the environmental situation on the roadside.

     

Chemical characterization of fine particles from on-road vehicles in the Wutong tunnel in Shenzhen, China

Vehicle populations in China have been increasing sharply since 1990s. Vehicle emissions including various gaseous pollutants and particulate matter cause deterioration of air quality. However, measurements of particulate mater from on-road vehicles in China are scarcely reported, and thus the chemical compositions of particles emitted from vehicles in China are unknown. In this research, tunnel experiments were performed to measure PM2.5 in the Wutong tunnel, Shenzhen, China. Detailed PM2.5 chemical compositions, with organic compounds determined by GC/MS, in the tunnel were presented. Elemental carbon and organic matter composed 63% and 34% of the total PM2.5 mass in the Wutong tunnel, respectively. Alkanes, PAHs, hopanes, fatty acids, and dicarboxylic acids were the major identified organic compounds, and their source profiles in the PM2.5 in the Wutong tunnel were characterized. The comparisons of our measurements with those in the literature were also made to demonstrate the characteristics of the vehicle source profiles in the Wutong tunnel. The experimental results in this paper can improve understanding of particulate matter emitted from vehicles in China.     

Seasonal variations of hydroxylated and methoxylated brominated diphenyl ethers in blue mussels from the Baltic Sea

Hydroxylated polybrominated diphenyl ethers (OH-PBDEs) and methoxylated polybrominated diphenyl ethers (MeO-PBDEs) found at high levels in the Baltic biota are mainly natural products, but can also be formed through metabolism or abiotic oxidation of polybrominated diphenyl ethers (PBDEs). The formation of OH-PBDEs is of concern since there is growing evidence of phenolic toxicity. This study investigates seasonal variations in levels of OH-PBDEs and MeO-PBDEs, focusing on an exposed species, the blue mussel (Mytilus edulis), sampled in the Baltic Sea in May, June, August and October of 2008. Both the OH-PBDE and MeO-PBDE levels in the mussels showed seasonal variations from May to October, the highest concentration of each congener appearing in June. The seasonal variation was more marked for OH-PBDEs than in MeO-PBDEs, but all congeners showed the same trends, except 6-MeO-BDE47 and 2′-MeO-BDE68, which did not significantly decline in concentrations after June. Biotic or abiotic debromination is suggested as a possible reason for the rapid decrease in methoxylated penta- and hexa-BDE concentrations observed in blue mussels from June to August, while the tetraBDE concentrations were stable. In addition, 1,3,7/1,3,8-tribrominated dibenzo-p-dioxins showed the same seasonal variation. The seasonal variations indicates natural formation and are unlikely to be due to transformation of anthropogenic precursors. The levels of PBDEs were fairly constant over time and considerably lower than those of the OH-PBDEs and MeO-PBDEs. The timing of the peaks in concentrations suggests that filamentous macro-algae may be important sources of these compounds found in the blue mussels from this Baltic Sea location.     

Ammonia emissions from different pig production scales and their temporal variations in the North China Plain

ABSTRACT

Pig production systems in China are shifting from small to industrial scale. Significant variation in housing ammonia (NH₃) emissions can exist due to differences in diet, housing design, and management practices. However, there is a knowledge gap regarding the impacts of farm-scale in China, which may be critical in identifying hotspots and mitigation targets. Here, continuous in-situ NH₃ concentration measurements were made at pig farms of different scales for sows and fattening pigs over periods of 3–6 days during two different seasons (summer vs. winter). For the sow farms, NH₃ emission rates were greater at the small farm (summer: 0.52 g pig^?1 hr^?1; winter: 0.21 g pig^?1 hr^?1) than at the large farm (summer: 0.34 g pig^?1 hr^?1; winter: 0.12 g pig^?1 hr^?1). For the fattening pig farms, NH₃ emission rates were greater at the large farm (summer: 0.22 g pig^?1 hr^?1; winter: 0.16 g pig^?1 hr^?1) than at the small farm (summer: 0.19 g pig^?1 hr^?1; winter: 0.07 g pig^?1 hr^?1). Regardless of farm scale, the NH₃ emission rates measured in summer were greater than those in winter; the NH₃ emission rates were greater in the daytime than at the nighttime; a positive relationship (R² = 0.06–0.68) was established between temperature and NH₃ emission rate, whereas a negative relationship (R² = 0.10–0.47) was found between relative humidity and NH₃ emission rate. The effect of farm-scale on indoor NH₃ concentration could mostly be explained by the differences in ventilation rates between farms. The diurnal variation in NH₃ concentration could be partly explained by ventilation rate (R² = 0.48–0.78) in the small traditional farms and by emission rate (R² = 0.26–0.85) in the large industrial farms, except for the large fattening pig farm in summer. Overall, mitigation of NH₃ emissions from sow farms should be a top priority in the North China Plain.

Implications: The present study firstly examined the farm-scale effect of ammonia emissions in the North China Plain. Of all farms, the sow farm was identified as the greatest source of ammonia emission. Regardless of farm scale, ammonia emission rates were observed to be higher in summer. Ammonia concentrations were mostly higher in the large industrial farms partly due to lower ventilation rates than in the small traditional farms.     

Road Dust Resuspension in the Vicinity of Limestone Quarries in Jordan

Abstract

Many areas in Jordan suffer from elevated levels of coarse particulate matter (PM₁₀). One potentially significant source of the observed PM is the resuspension of road dust in the vicinity of limestone quarries. To obtain data to assess the impact from this source, PM₁₀ road dust resus-pension factors near Abusiiah, a town to the north east of Amman surrounded by many quarries and brick factories, were measured. Measurements included PM₁₀ mass, particle size distributions, wind speed, and wind direction.The results showed that PM₁₀ concentrations could be as high as 600 µg/m³, and most of the airborne PM is in the coarse fraction. Loading trucks play a major role in resus-pending road dust, with an observed PM₁₀ emission rate of >6000 mg/km.     

Interspecific and geographical variations of trace element concentrations in Pectinidae from European waters

Cd, Cu and Zn were analysed in the organs and tissues of the three scallop species from the Bay of Biscay, the variegated Chlamys varia L., the queen scallop Aequipecten opercularis L. and the common scallop Pecten maximus L. for interspecific comparisons. In P. maximus the greatest concentrations of Cd and Cu were found in the digestive gland, whereas the two other species showed similar levels of Cd between digestive gland and kidneys and higher renal Cu concentrations. However, the digestive gland of all Pectinidae species contained from 75% to 93% and 52% to 74% of the total body burdens of Cd and Cu, respectively. Whatever the species, kidneys displayed the highest Zn concentrations, which therefore contained from 53% to 97% of the total body burden of this metal. Also using reported results, ratios between the concentrations in the digestive gland and that in the kidneys discriminated two groups of Pectinidae: (1) the Pecten group (P. maximus, P. jacobeus and Adamussium colbecki) with a Cd ratio > or = 4, a Cu ratio > or = 1 and a Zn ratio > 20x10(-3); (2) the Chlamys group with a Cd ratio < or = 1, a Cu ratio < or = 1 and a Zn ratio < or = 6x10(-3). However, no differences in the detoxification processes in the digestive gland were found between groups in this study. 72-80% of the total Cd was found to be soluble, probably bound to metalloproteins such as metallothioneins, while Cu and Zn were mainly found associated to the insoluble fraction of the digestive gland cells whatever the species. Queen scallops from the Faroe Islands were also considered to examine variations of the metal concentrations due to the geographical origin. In this northern area, queen scallops displayed Cd concentrations 2, 4 and 6 times higher in kidneys, muscle and digestive gland, respectively, compared to those from the Bay of Biscay. Consequently, the Cd concentrations in the whole soft parts of the queen scallops were more than 6 times higher in the Faroe Islands than in the Bay of Biscay. In contrast to Cd, both Cu and Zn concentrations in the whole soft parts were 2 times lower in the Faroe Islands, suggesting lower bioavailability of these essential elements.