Characterizing Indoor and Outdoor 15 Minute Average PM 2.5 Concentrations in Urban Neighborhoods

While a number of studies have looked at the relationship between outdoor and indoor particulate levels based on daily (24 h) average concentrations, little is known about the within-day variability of indoor and outdoor PM levels. It has been hypothesized that brief airborne particle excursions on a time scale of a few minutes to several hours might be of health significance. This article reports variability in measurements of daily (24 h) average PM 2.5 concentrations and short-term (15 min average) PM 2.5 concentrations in outdoor and indoor microenvironments. Daily average PM 2.5 concentrations were measured using gravimetry, while measurements of 15 min average PM 2.5 mass concentrations were made using a light scattering photometer whose readings were normalized using the gravimetric measurements. The measurements were made in 3 urban residential neighborhoods in the Minneapolis-St. Paul metropolitan area over 3 seasons: spring, summer, and fall of 1999. Outdoor measurements were made at a central monitoring site in each of the 3 communities, and indoor measurements were made in 9-10 residences (with nonsmoking occupants) in each community. Residential participants completed a baseline questionnaire to determine smoking status, sociodemographics, and housing characteristics. Outdoor PM 2.5 concentrations across the Minneapolis-St. Paul metropolitan area appear to be spatially homogeneous on a 24 h time scale as well as on a 15 min time scale. Short-term average outdoor PM 2.5 concentrations can vary by as much as an order of magnitude within a day. The frequency distribution of outdoor 15 min averages can be described by a trimodal lognormal distribution, with the 3 modes having geometric means of 1.1 w g/m 3 (GSD = 2.1), 6.7 w g/m 3 (GSD = 1.6), and 20.8 w g/m 3 (GSD = 1.3). There is much greater variability in the within-day 15 min indoor concentrations than outdoor concentrations (as much as ～40-fold). This is most likely due to the influence of indoor sources and activities that cause high short-term peaks in concentrations. The indoor 15 min averages have a bimodal lognormal frequency distribution, with the 2 modes having geometric means of 8.3 w g/m 3 (GSD = 1.66) and 35.9 w g/m 3 (GSD = 1.8), respectively. The correlation between the matched outdoor and indoor 15 min average PM 2.5 concentrations showed a strong seasonal effect, with higher values observed in the spring and summer ( R 2 adj = 0.49 - 0.33) and lower values in the fall ( R 2 adj = 0.13 - 0.13).     

Development and evaluation of a palm-sized optical PM2.5 sensor

A new palm-sized optical PM_2.5 sensor has been developed and its performance evaluated. The PM_2.5 mass concentration was calculated from the distribution of light scattering intensity by considering the relationship between scattering intensity and particle size. The results of laboratory tests suggested that the sensor can detect particles with diameters as small as ～0.3 µm and can measure PM_2.5mass concentrations as high as ～600 µg/m³. Year-round ambient observations were conducted at four urban and suburban sites in Fukuoka, Kadoma, Kasugai, and Tokyo, Japan. Daily averaged PM_2.5 mass concentration data from our sensors were in good agreement with corresponding data from the collocated standard instrument at the Kadoma site, with slopes of 1.07–1.16 and correlation coefficients (R) of 0.90–0.91, and with those of the nearest observatories of the Ministry of the Environment of Japan, at 1.7–4.1 km away from our observation sites, with slopes of 0.97–1.23 and R of 0.89–0.95. Slightly greater slopes were observed in winter than in summer, except at Tokyo, which was possibly due to the photochemical formation of relatively small secondary particles. Under high relative humidity conditions (>70%), the sensor has a tendency to overestimate the PM_2.5 mass concentrations compared to those measured by the standard instruments, except at Fukuoka, which is probably due to the hygroscopic growth of particles. This study demonstrates that the sensor can provide reasonable PM_2.5 mass concentration data in urban and suburban environments and is applicable to studies on the environmental and health effects of PM_2.5.

Copyright © 2018 American Association for Aerosol Research     

Indoor Sources of Ultrafine and Accumulation Mode Particles: Size Distributions,Size-Resolved Concentrations,and Source Strengths

Ultrafine (< 100 nm) and accumulation mode (0.1–1 μm) particles were monitored in an occupied suburban house at 5-minute intervals for 37 consecutive months between November 21, 1997 and December 31, 2000. Number concentrations for 126 particle sizes from 9.8–947 nm were measured in 259,176 scans. Of 282 separate activities, 18 were chosen for detailed analysis. These included cooking with a gas stove, toasting with electric toasters and toaster ovens, burning candles and incense, and using a gas-powered clothes dryer. Activities leading to increased particle concentrations occurred 17.5% of the time, and accounted for more than half the total concentration of ultrafines and about a quarter of the total accumulation mode particles. The average duration of elevated particle concentrations ranged from 20 minutes to 3 hours. Combustion of natural gas (boiling water, gas clothes dryer) showed number peaks near 10 nm, while the electric toaster and toaster oven had peaks close to 30 nm. More complex cooking (burners plus gas oven) produced peaks in the 35–50 nm range. Burning candles and incense resulted in peaks in the 60-nm range. Finally, outdoor sources peaked at nearly 70 nm, indicating the influence of aging in shifting modes to higher diameters. The highest mean number concentrations were due to complex cooking, producing average number concentrations of 35,000–50,000 cm^{? 3}, compared to 12,000 cm^?3 outdoors and less than 3500 cm^?3 indoors when no sources were observed. A strong contribution of the vented gas-powered clothes dryer was also noted (30,000 cm^{? 3}). Volume concentrations due to these combustion events ranged from < 1 (μm/cm)³ to nearly 100 (μm/cm)³. Source strengths were calculated for three common cooking types (boiling water, deep-frying, oven baking, and broiling) and ranged from 5 × 10 ¹² to 4 × 10 ¹³ particles per cooking event. The detailed concentration and size distribution data collected here may be useful for models of indoor air particle concentrations due to indoor sources and infiltration.     

Structural and electrical properties of magnetic ceramics of Co1−xCuxFe2O4 spinel nanoferrites

Abstract

Magnetic ceramics of the type of spinel nanoferrites of Co_1?xCu_xFe₂O₄ with Cu concentrations of x?=?0·00, 0·25, 0·50, 0·75 and 1·00 were prepared by chemical co-precipitation method. X-ray diffraction results confirmed the formation of a single spinel ferrite structure with crystallite size in the range of 20–63 nm. Scanning electron microscopy and EDS were used to study the morphological and compositional changes taking place with varying Cu concentration. DC electrical resistivity, activation energy and drift mobility are strongly influenced by both Cu concentration and temperature. Resistivities of the prepared magnetic ceramics were found to decrease with the increase in Cu concentration to follow Verwey mechanism. The semiconductor behaviour of the prepared nanoparticles was confirmed from the standard Arrhenius relation of resistivity versus temperature. The dielectric constants were measured in the frequency range of 100 Hz–3·0 MHz and are explained by the Maxwell–Wagner interfacial type of polarisation.     

Concentration and Size Distribution of Culturable Airborne Microorganisms in Outdoor Environments in Beijing,China

A one-year (from June 2003 to May 2004) study of airborne microbial concentration and size distribution was conducted systematically at three selected sampling sites in Beijing. Microbial samples were collected in triplicate for 3 min, 3 times per day, for 3 consecutive days of each month using FA-I sampler (imitated Andersen sampler, made by Applied Technical Institute of Liaoyang, China). Results showed that the concentration of total culturable microorganisms ranged from 4.8 × 10 ² colony forming units (CFU)/m ³ to 2.4 × 10 ⁴ CFU/m ³ , with an arithmetic mean of 3.7 × 10 ³ ± 2.1 × 10 ² (standard deviation) CFU/m ³ . As a whole, the percentage of airborne bacteria, accounting for 59.0% of the total culturable microorganisms, was significantly higher than those of airborne fungi (35.2%) and actinomycetes (5.8%). At RCEES (Research Center for Eco-Environmental Sciences—a culture and education area) and XZM (Xizhimen—a main traffic line), significantly higher percentages of airborne bacteria were found as compared to airborne fungi. No significant difference was observed between airborne bacteria and fungi at BBG (Beijing Botanical Garden—a green garden area). The total microbial concentration was significantly higher at RCEES than at XZM and BBG (*P < 0.05), and no significant difference between XZM and BBG was observed (P > 0.05). Total microbial concentrations were higher in summer and autumn, and lower in spring and winter at RCEES and XZM (*P < 0.05). At BBG, higher concentration was observed in summer during the sampling periods (***P < 0.001). The size distribution of airborne bacteria showed a skewed distribution at three sampling sites. The proportion of bacterial particles decreased gradually from Stage 1 ( > 7.0 μm) to Stage 6 (0.65 ～ 1.1 μm), and there was an obvious downtrend on Stage 2 (4.7 ～ 7.0 μm). Bacterial particles were mainly distributed at the first four Stages ( > 2.1 μm), accounting for 78.6% at RCEES, 84.0% at XZM, and 81.5% at BBG. The size distribution pattern of airborne fungi was found with normal logarithmic distribution at three sampling sites. Fungal particles were mainly distributed at Stage 3 (3.0 ～ 6.0 μ m), Stage 4 (2.0 ～ 3.5 μ m) and Stage 5 (1.0 ～ 2.0 μ m), composing 71.6% of the population at RCEES, 74.2% at XZM, and 68.3% at BBG. However, different distribution patterns were found in different dominant fungal genera. Cladosporium, Penicillium, and Aspergillus were present with normal logarithmic distribution, while Alternaria and sterile mycelia were found with skewed distribution. In opposition to the distribution pattern of fungal particles, the actinomycete particles at all sampling sites were primarily collected on Stage 1, Stage 5, and Stage 6, accounting for 61.1% at RCEES, 60.7% at XZM, and 64.8% at BBG.     

Dominant Mechanisms that Shape the Airborne Particle Size and Composition Distribution in Central California

The size and composition of ambient airborne particulate matter is reported for winter conditions at five locations in (or near) the San Joaquin Valley in central California. Two distinct types of airborne particles were identified based on diurnal patterns and size distribution similarity: hygroscopic sulfate/ammonium/nitrate particles and less hygroscopic particles composed of mostly organic carbon with smaller amounts of elemental carbon. Daytime PM₁₀ concentrations for sulfate/ammonium/nitrate particles were measured to be 10.1 μ g m^?3, 28.3 μ g m^?3, and 52.8 μ g m^?3 at Sacramento, Modesto and Bakersfield, California, respectively. Nighttime concentrations were 10–30% lower, suggesting that these particles are dominated by secondary production. Simulation of the data with a box model suggests that these particles were formed by the condensation of ammonia and nitric acid onto background or primary sulfate particles. These hygroscopic particles had a mass distribution peak in the accumulation mode (0.56–1.0 μ m) at all times. Daytime PM₁₀ carbon particle concentrations were measured to be 9.5 μ g m^?3, 15.1 μ g m^?3, and 16.2 μ g m^?3 at Sacramento, Modesto, and Bakersfield, respectively. Corresponding nighttime concentrations were 200–300% higher, suggesting that these particles are dominated by primary emissions. The peak in the carbon particle mass distribution varied between 0.2–1.0 μ m. Carbon particles emitted directly from combustion sources typically have a mass distribution peak diameter between 0.1–0.32 μ m. Box model calculations suggest that the formation of secondary organic aerosol is negligible under cool winter conditions, and that the observed shift in the carbon particle mass distribution results from coagulation in the heavily polluted concentrations experienced during the current study. The analysis suggests that carbon particles and sulfate/ammonium/nitrate particles exist separately in the atmosphere of the San Joaquin Valley until coagulation mixes them in the accumulation mode.     

SO2 absorption/desorption performance of renewable phenol-based deep eutectic solvents

Six renewable DESs prepared from choline chloride (CC) and phenols (guaiacol, GC; cardanol, CL) with molar ratios of phenols to CC of 3:1, 4:1 and 5:1 were investigated to absorb SO₂ at 293.15–323.15 K and 0–1.0 bar. Results showed that DESs demonstrated satisfactory SO₂ absorption performance, and GC–CC (3:1) exhibited the maximum absorption capacity of 0.528 g SO₂ per g DES. The SO₂ enriched DESs could be easily regenerated and recycled five times. Moreover, the DESs exhibited high selectivity of SO₂/CO₂. Present DESs seem to be promising absorbents for SO₂ due to good performance.     

Wavelength Dependence of the Aerosol Angstrom Exponent and Its Implications Over Delhi,India

The aerosol optical depth (AOD), Angstrom coefficients (α and β), and the second-order Angstrom exponent (α′) obtained by Microtops-II sun photometer have been analyzed in the spectral range 0.34–0.87 μm over the urban polluted city of Delhi, India for the period 2007–2008, aiming at investigating the physical and optical properties of aerosols. The average values of AOD at 500 nm, α and β (in the range 340–870 nm) are found to be 0.78 ± 0.32, 0.78 ± 0.28, and 0.45 ± 0.21, respectively, for the entire period of observations. The AOD data show significant curvature in the lnτ versus lnλ relationship suggesting different dominant aerosol types depending on season. In order to analyze further the curvature effect and the relative dominance of aerosol size, α has been calculated in three wavelength bands, i.e., shorter (0.34–0.50 μm), longer (0.675–0.87 μm), and broad (0.34–0.87 μm) during four seasons, summer (April–June), monsoon (July–September), winter (October–January), and spring (February–March) accompanied with calculations of α′, which quantifies the deviation of logarithmic behavior of AOD with lnλ. The α′ values are found to be positive and higher in the months of October–December and mostly negative in February and March, while close to zero values of α′ are found in April–August. These results indicate that winter season exhibits dominance of fine-mode aerosols while summer relatively higher concentration of coarse-mode particles. On the other hand, monsoon and spring seasons revealed the presence of mixed type, both fine- and coarse-mode aerosols over Delhi.     

Associations of Fungal Aerosols,Air Pollutants,and Meteorological Factors

The relationships between fungal aerosols and air pollutants meteorological factors were investigated in the Taipei urban area. In summer, it was observed that geometric mean (GM) concentrations of airborne fungal aerosols were 2,835 CFU m^-3 and 2,651 CFU m^-3 at Kuting and Hsichih stations, respectively. In winter, GM levels of airborne fungi were 1,107 CFU m I 3 and 2,248 CFU m^-3 at Kuting and Hsichih stations, respectively. Moreover, fungal aerosol concentrations were observed to highly depend on weather conditions, and the highest concentration of total colony counts appeared when the temperature was 25-30 C, the RH was 60-70% , and the wind speed was > 1 m s^-1 and from the S-SE wind direction. In addition, total fungal concentrations were negatively correlated with ozone concentrations, and concentration of Cladosporium spp. was positively correlated with hydrocarbons. PM₁₀ were positively correlated with Penicillium and the yeasts in Hsichih station. Our results demonstrated that airborne fungal aerosols are definitely correlated with air pollutants and meteoro logical factors. The complex dynamic interactions were indicated to occur among bioaerosols, air pollutants, and meteorological factors.     

Sequestration of CO2 using microorganisms and evaluation of their potential to synthesize biomolecules

ABSTRACT

Microalgae are the unicellular or multicellular photosynthetic microorganisms that can efficiently fix carbon dioxide (CO₂) from various sources such as the environment, industrial flue gas, and some carbonate salts. In the present study, one green microalgal strain and a cyanobacterial consortium were used separately for the sequestration of CO₂ at different pHs (7–11), at different initial concentrations of CO₂ (5–20%), and at various inoculum sizes (5–12.5%). The maximum sequestration of CO₂ was found to be 74.37 ± 0.49% and 71.12 ± 0.05% at 5% and 15% CO₂ for green algae and cyanobacterial consortium. The biomass generated after sequestration of CO₂ was utilized for the synthesis of biomolecules.     

Surfactants in sediment of Itanhaém Estuary,São Paulo,Brazil

This study investigated surfactant levels in the sediment of Itanhaém Estuary through colorimetric methods with methylene blue active substances (MBAS). Samples were collected with a Van Veen bottom sampler at eight sampling points during autumn, winter, and spring of 2015. The results demonstrate growing detergent deposition in the sediment of the estuary. Surfactant concentration was higher (16.18 μg MBAS g⁻¹) around the sewage treatment plant (STP) than in the estuary in autumn, after the vacation/summer season when the population of the city had increased due to tourism. There was a significant (p < 0.05) reduction in detergent concentration (to 14.94 μg MBAS g⁻¹) in winter, after school vacation, while in spring the surfactants concentration for the STP was high only for the sampling points nearer the ocean. Surfactant concentrations differed significantly among sampling points (p < 0.05), with them being higher at those closer to the STP. Enrichment with high loads from anthropogenic sources associated with urbanization and tourism was responsible for the greater surfactant concentrations in areas near the STP. In conclusion, more efficient treatment of domestic effluent of the city of Itanhaém is needed, as is the control of clandestine discharge into the river since the accumulation of detergents in sediment can have harmful effects on aquatic life.     

Evaluation of a Denuder-MOUDI-PUF Sampling System to Measure the Size Distribution of Semi-Volatile Polycyclic Aromatic Hydrocarbons in the Atmosphere

This study describes a field comparison conducted between 2 methods employing different MOUDI impactor configurations to evaluate their performance in sampling and measurement of the size distribution of 15 priority pollutant polycyclic aromatic hydrocarbons (PAHs). Samples were collected during 24 h periods approximately every 7th day, beginning at 8:00 AM, in 2 different sites of the Los Angeles Basin. One site was near Central Los Angeles in an area impacted by high vehicular traffic, whereas the other site was located about 60 km downwind of central Los Angeles (receptor site). Particle samples from about 43 m 3 of air were collected using collocated MOUDI impactors and classified in 3 aerodynamic diameter size intervals: 0-0.18 w m (ultrafine mode I), 0.18-2.5 w m (accumulation mode II), and 2.5-10 w m (coarse mode III). One MOUDI operated in the conventional mode, the other with a vapor trapping system that included an XAD-4 coated annular denuder placed upstream of the impactor and a polyurethane foam plug (PUF) placed in series behind the impactor. PAHs were separated and quantified by HPLC with fluorescence detection optimized for the highest sensitivity. The results showed that for both sites, using either sampling system, the size distributions obtained are similar for the less volatile PAHs (log [ p ° L ] h m 3.2), but different for the more volatile PAHs (log [ p ° L ] S m 2.06). In the central Los Angeles site, the largest PAH fraction was found in the 0-0.18 w m (mode I) size range, typical of primary emissions. At the downwind location, the largest fraction was in the 0.18-2.5 w m (mode II) size range, consistent with an "aged" aerosol. At both sites, albeit not statistically significant, the mean regular to denuded MOUDI mass ratios were 33-36% and 11-19% higher, respectively, for the more volatile and the less volatile PAH groups. Sampling with the regular MOUDI configuration is simpler and thus recommended for measurement of the size distribution of PAHs in either group.     

Observations of Twelve USEPA Priority Polycyclic Aromatic Hydrocarbons in the Aitken Size Range (10–32 nm D p )

Particle size distribution measurements of twelve USEPA priority pollutant polycyclic aromatic hydrocarbons (PAHs)—collected in Riverside, California, down to 10 nm aerodynamic diameter (D_p)—observed on integrated nocturnal samples (7:00 p.m.-6:30 a.m.) revealed that between 46 and 100% of the mass of particles in the Aitken size range was found in the 10–18 nm size bin. Particles in this size range have high alveolar deposition efficiency.     

DISTRIBUTION DATA FOR THE SYSTEM Th(NO3)4:UO2(NO3)2:HNO3/30 % TBP IN DODECANE

Abstract

Distribution data for the systems Th(NO₃)₄:HNO₃/30 % TBP in dodecane and Th(NO₃)₄:UO₂(NO₃)₂:HNO₃/30 % TBP in dodecane have been evaluated experimentally. By means of these data a caleulationa1 model has been derived which makes it possible to determine data in the investigated range. A method is also described for the evaluation of distribution data at very low thorium concentrations.     

Direct thermal drying of sludge using flue gas and its environmental benefits

This paper reported a sludge disposal technology that uses 100–200°C flue gas to dry sludge through a systematic analysis of the relationship between sludge drying rate/temperature and moisture content. Using this direct drying technology, the sludge drying capacity for the dryer tested can reach 86?tons?d^?1 at 160°C. The experimental results show this technology can also preserve 95% calorific value in the sludge, and remove 16–42% PM_2.5, 26–55% PM₁₀, and 7–25% SO₂ from the flue gas. The exhaust gas from the sludge dryer consists mainly of chain alkanes while benzenes only 9.65% when dried at 100°C.     

Characterization of Radioactive Aerosols in Florida Phosphate Processing Facilities

The health risks to workers in the Florida phosphate industry resulting from chronic inhalation of radionuclide-containing aerosols have not been adequately addressed. The present study establishes a database of information on the particle size distribution, density, shape, chemical composition, and radioactivity concentration for six phosphate facilities in the northern and central regions of the state. A seven-stage cascade impactor was employed to sample aerosols at various processing areas in these plants. Aerosol mass loadings are lowest mainly at shipping areas where they are approximately one order of magnitude less than at granulator areas within equivalent particle size intervals. Aerosol mass concentrations increase as the aerosol size increases for the majority of the plants and operational areas. The aerosol loading at each area varies widely depending on plant, and the variance is largest at the storage areas due to the variability of mechanical operations and patterns of building ventilation. The density of bulk dry product, settled dust, and airborne particles are between 1.6 to 1.7 g/cm ³ . Under electron microscopy, the particles appear as spheroids or rough spherical fragments across all plants, work areas, and sampled size intervals. The main elemental components of large-sized and medium-sized aerosols are similar to those found in the bulk dry product. For small-sized aerosols (0.2–0.4 μ m), the fraction of phosphorus is very small in comparison to elemental impurities such as silicon and sulfur. The ²³⁸ U decay series was found in both bulk dry product, settled dust, and airborne particles collected via high-volume samplers. The ²³⁸ U, ²²⁶ Ra, and ²¹⁰ Pb radioactivity concentrations in bulk dry product and settled dust from central Florida range from 63–112 pCi/g, 0.8–1.5 pCi/g, and 7–9 pCi/g, respectively. No significant differences in the radioactivity concentrations of ²³⁸ U and ²²⁶ Ra were found between dry product, settled dust, and sampled aerosols. However, ²¹⁰ Pb is highly concentrated in aerosols up to 25–87 pCi/g, most likely due to the deposition of ambient airborne radon decay products on workplace aerosols. The database of worker aerosol physicochemical characteristics established in this study for the Florida phosphate industry can be directly used for more realistic assessments of worker inhalation dose, thus providing a more firm basis for assessing the adequacy of existing respiratory and other radiological protection policies.     

A case study on suspended particles in a natural gas urban transmission and distribution network

Suspended particles in the natural gas transmission and distribution network of the city of Kerman, Iran were investigated. Particle concentration and size distribution were measured in different locations of the natural gas pipeline network. Particle samplings were carried out in two seasons: summer, when there is the lowest consumption, and winter, when there is the highest consumption of natural gas. Additional particle characterization was carried out by scanning electron microscopy coupled with energy dispersion X-ray (SEM/EDX) and X-ray diffraction(XRD) analyses. Particle concentration was found to be significantly higher in winter as compared to summer. The range of particle concentrations in summer was from 0.12 mg/Nm³ at the end of the pipeline to 4.7 mg/Nm³ at the network entrance, and from 0.30 mg/Nm³ to 22.1 mg/Nm³ in winter. Particle size distribution showed a higher frequency of smaller particles in winter than in summer. Larger particles were more likely to exist at the network entrance as compared to the exit. The average particle size ranged from 181 μm at the network end to 253 μm at the entrance in summer, and from 74 μm to 209 μm in winter. Particle characterization confirmed the presence of corrosion products in the suspended particles.     

Preparation of Al2O3–SiC composite powder from kyanite tailings via carbothermal reduction process

ABSTRACT

Al₂O₃–SiC composite powders were prepared from kyanite tailings mixed with 20% excess carbon coke via carbothermal reduction (CR) reaction. The optimised synthesis condition for synthesising Al₂O₃–SiC composite powders was at 1600°C for 6?h. The equilibrium relationship curves of the condensed phases were presented and the temperature dependence of the phase composition was also studied. The results show that irregular Al₂O₃ and SiC grains first formed at 1500°C, and the elements C, O, Al, and Si randomly distributed in the each crystal particles. The amount of Al₂O₃–SiC composites increased with the increasing synthesis temperature and reaction time. Finally, Al₂O₃–SiC composite bulk materials were further prepared by pressureless sintering using the synthesised Al₂O₃–SiC composite powders as raw materials, and their mechanical properties were investigated in detail. All these results indicate that the CR method can offer a niche application for the development of kyanite tailings.     

Wire-mesh honeycomb catalysts for selective catalytic reduction of NO with NH3

Both flat and corrugated wire mesh sheets were coated with aluminum powder by using electrophoretic deposition (EPD) method. Controlled thermal sintering of coated samples yielded uniform porous aluminum layer with a thickness of 100 μm that was attached firmly on the wire meshes. Subsequent controlled calcination formed a finite thickness of Al₂O₃ layer on the outer surface of each deposited aluminum particles, which resulted in the formation of Al₂O₃/Al double-layered composite particles that were attached firmly on the wire surface to form a certain thickness of porous layer. A rectangular-shaped wire-mesh honeycomb (WMH) module with triangular-shaped channels was manufactured by packing alternately the flat sheet and corrugated sheet of the Al₂O₃/Al-coated wire meshes. This WMH was further coated with V₂O₅-MoO₃-WO₃ catalyst by wash-coating method to be applied for the selective catalytic reduction (SCR) of NO with NH₃. With an optimized catalyst loading of 16 wt%, WMH catalyst module shows more than 90% NO conversion at 240 °C and almost complete NO conversion at temperatures higher than 300 °C at GHSV 5,000 h⁻¹. When compared with conventional ceramic honeycomb catalyst, WMH catalyst gives NO conversion higher by 20% due to reduced mass transfer resistance by the existence of three dimensional opening holes in WMH.