Size-dependent characteristics of diurnal particle concentration variation in an underground subway tunnel.

Understanding characteristics of diurnal particle concentration variation in an underground subway tunnel is important to reduce subway passengers' exposure to high levels of toxic particle pollution. In this study, real-time particle monitoring for eight consecutive days was done at a shelter located in the middle of a one-way underground subway tunnel in Seoul, Republic of Korea, during the summer of 2015. Particle mass concentration was measured using a dust monitor and particle number concentration using an optical particle counter. From the diurnal variations in PM10, PM2.5, and PM1, concentrations of particles larger than 0.54 µm optical particle diameter were affected by train frequency whereas those of particles smaller than 0.54 µm optical particle diameter were not changed by train frequency. Number concentration of particles smaller than 1.15 µm optical particle diameter was dependent on outdoor ambient air particle concentration level, whereas that of particles larger than 1.15 µm optical particle diameter was independent of outdoor ambient air due to low ventilation system transmission efficiency of micrometer-sized particles. In addition, an equation was suggested to predict the diurnal particle concentration in an underground tunnel by considering emission, ventilation, and deposition effects.

Electrospun Magnetic Nanoparticle-Decorated Nanofiber Filter and Its Applications to High-Efficiency Air Filtration.

Filtration technology has been widely studied due to concerns about exposure to airborne dust, including metal oxide nanoparticles, which cause serious health problems. The aim of these studies has been to develop mechanisms for the continuous and efficient removal of metal oxide dusts. In this study, we introduce a novel air filtration system based on the magnetic attraction force. The filtration system is composed of a magnetic nanoparticle (MNP)-decorated nanofiber (MNP-NF) filter. Using a simple electrospinning system, we fabricated continuous and smooth electrospun nanofibers with evenly distributed Fe3O4 MNPs. Our electrospun MNP-NF filter exhibited high particle collection efficiency (∼97% at 300 nm particle size) compared to the control filter (w/o MNPs, ∼ 68%), with a ∼ 64% lower pressure drop (∼17 Pa) than the control filter (∼27 Pa). Finally, the filter quality factors of the MNP-NF filter were 4.7 and 11.9 times larger than those of the control filter and the conventional high-efficiency particulate air filters (>99% and ∼269 Pa), respectively. Furthermore, we successfully performed a field test of our MNP-NF filter using dust from a subway station tunnel. This work suggests that our novel MNP-NF filter can be used to facilitate effective protection against hazardous metal oxide dust in real environments.

Generation of Nanoparticles from Friction between Railway Brake Disks and Pads.

In this study, we measured the size distribution of particles ranging in size from 5.6 to 560 nm that were emitted between brake disks and pads under various braking conditions to observe and analyze changes to the resulting particle size distribution over braking time. A peak of 178-275 nm (200 nm peak) was observed in all braking conditions. However, the generation of spherical particles of a 10 nm range was observed only when the disk speed and brake force were above certain levels and intensified only when speed and brake force further increased. The total number concentration of ultrafine particles (no larger than 0.1 µm; PM0.1) generated was found to correlate with disk speed and brake force. Thus, the generation of nanoparticles resulting from disk speed and brake force was attributable primarily to increases in the contact surface temperature. The critical temperature for the generation of nanoparticles of a 10 nm range was found to be about 70 °C, which is the average temperature between the surface and the inside of the disk. If the speed or brake force was higher, that is, the temperature of the contact surface reached a certain level, evaporation and condensation took place. Vapor then left the friction surface, met with the air, and quickly cooled to form nanoparticles through nucleation. When the newly generated particles became highly concentrated, they grew through coagulation to form agglomerates or the vapor condensed directly onto the surface of existing particles of about 200 nm (formed by mechanical friction).

Aerosol-Processed Nanomaterials for Antimicrobial Air Filtration.

Health-care products are a dominant application of various nanotechnologies. Silver nanoparticles are widely used in commercial products requiring antimicrobial activity. Due to the limitations of wet processing in nanotechnology applications, dry aerosol processes have been developed for indoor antimicrobial air filtration. In this work, various aerosol processes for the synthesis or generation of nanomaterials, natural-product nanoparticles, and hybrid nanoparticles are reviewed. Key aerosol processes and the morphologies of various antimicrobial nanoparticles generated using a variety of systems or deposited on filter fibers are introduced.

Detection of Carbonaceous Aerosols Released in CNT Workplaces Using an Aethalometer.

OBJECTIVES: Black carbon (BC) originating from various combustion sources has been extensively surveyed to characterize the effects of BC on global warming and human health, and many online monitors are available. In this study, BC was considered as a surrogate for carbon-based nanomaterials in an occupational health study. METHODS: Specifically, BC concentrations were monitored continuously with an aethalometer for 24h at four carbon nanotube (CNT) workplaces located in rural, urban, and industrial areas, which had different background air pollution levels. Average BC concentrations for both nonworking (background) and working periods were compared with the recommended exposure limit (REL) of 1 µg m(-3) for elemental carbon that was suggested by the National Institute for Occupational Safety and Health (NIOSH). RESULTS: Diurnal variation of BC concentrations indicated that BC measurements corresponded well with carbonaceous aerosols such as vehicle exhaust particles and CNT aerosols. In the rural CNT workplace, the average background BC concentration (0.36 µg m(-3)) was lower than the REL, but the BC concentration without background correction was higher than the REL during manufacturing hours. In this case, BC measurement is useful to estimate CNT exposure for comparison with the REL. Conversely, in the urban and industrial CNT workplaces, average background BC concentrations (2.05, 1.82, and 2.64 µg m(-3)) were well above the REL, and during working hours, BC concentrations were substantially higher than the background level at workplace C; however, BC concentrations showed no difference from the background levels at workplaces B and D. In these cases (B and D), it is hard to determine CNT exposure because of the substantial environmental exposures. CONCLUSION: Most of the urban ambient BC concentrations were above the REL. Therefore, further analysis and test methods for carbonaceous aerosols need to be developed so that the exposure assessment can be easily carried out at CNT workplaces with high background BC levels such as in urban and industrial areas.

Synthesis of hybrid carbon nanotube structures coated with Sophora flavescens nanoparticles and their application to antimicrobial air filtration.

Controlling airborne microorganisms has become increasingly important with increase in human indoor activities, epidemic disease outbreaks, and airborne pathogen transmission. Treatments using antimicrobial nanoparticles have shown promise because of the high surface-to-volume ratio of nanoparticles compared to their bulk counterparts, and their unique physical and chemical properties. In this study, hybrid nanostructures of multi-walled carbon nanotubes (MWCNTs) coated with antimicrobial, natural product (NP) nanoparticles were synthesized using a twin-head electrospray system (THES). The coated nanoparticles were then used in antimicrobial air filters to increase their antimicrobial efficiency. Electrosprayed droplets were converted to NP nanoparticles and MWCNTs through ethanol evaporation. Oppositely charged NP nanoparticles and MWCNTs were coagulated via Coulombic collisions to form hybrid nanoparticles that were deposited continuously onto an air filter medium. The size distribution and composition of the hybrid NP/MWCNT particles were characterized using a wide-range particle spectrometer (WPS) and transmission electron microscope (TEM). The concentration of hybrid NP/MWCNT nanoparticles was lower than that of NP nanoparticles but higher than that of MWCNTs and showed a bimodal size distribution with peak diameters of 21.1 and 49 nm. TEM analyses confirmed that the NP nanoparticles were attached to the MWCNT surface with a density of ~4-9 particles/MWCNT. When deposited onto the filter medium, NP/MWCNT particles formed dendrites on the filter׳s fiber surface. The filtration efficiency and pressure drop of the NP/MWCNT-coated filters were higher than those of pristine, NP nanoparticles-coated or MWCNTs-coated filters. The hybrid filter also exhibited stronger antimicrobial activity than those of NP or MWCNT-coated filters at identical deposited volumes (1.1×10-2 cm3/cm2 filter). Ninety-five percent of the tested bacterial aerosols were inactivated on the NP/MWCNTs filter while only <70% were inactivated on NP- or MWCNT-coated filters.

Exposure Characteristics of Nanoparticles as Process By-products for the Semiconductor Manufacturing Industry.

This study aims to elucidate the exposure properties of nanoparticles (NPs; <100 nm in diameter) in semiconductor manufacturing processes. The measurements of airborne NPs were mainly performed around process equipment during fabrication processes and during maintenance. The number concentrations of NPs were measured using a water-based condensation particle counter having a size range of 10-3,000 nm. The chemical composition, size, and shape of NPs were determined by scanning electron microscopy and transmission electron microscopy techniques equipped with energy dispersive spectroscopy. The resulting concentrations of NPs ranged from 0.00-11.47 particles/cm(3). The concentration of NPs measured during maintenance showed a tendency to increase, albeit incrementally, compared to that measured during normal conditions (under typical process conditions without maintenance). However, the increment was small. When comparing the mean number concentration and standard deviation (n ± σ) of NPs, the chemical mechanical polishing (CMP) process was the highest (3.45 ± 3.65 particles/cm(3)), and the dry etch (ETCH) process was the lowest (0.11 ± 0.22 particles/cm(3)). The major NPs observed were silica (SiO2) and titania (TiO2) particles, which were mainly spherical agglomerates ranging in size from 25-280 nm. Sampling of semiconductor processes in CMP, chemical vapor deposition, and ETCH reveled NPs were <100 nm in those areas. On the other hand, particle size exceeded 100 nm in diffusion, metallization, ion implantation, and wet cleaning/etching process. The results show that the SiO2 and TiO2 are the major NPs present in semiconductor cleanroom environments.

Catalytic oxidation of benzene with ozone over Mn/KIT-6.

Benzene is one of the target compounds to be removed from air owing to its carcinogenicity. In this study, benzene oxidation with ozone over a MnOx/KIT-6 catalyst was carried out for the first time. MnOx/KIT-6 was synthesized using two different Mn precursors: Mn acetate and Mn nitrate. The characteristics of the synthesized catalysts were examined by X-ray diffraction, X-ray photoelectron spectroscopy, temperature-programmed reduction, Brunauer-Emmett-Teller (BET) surface area, and N2 adsorption-desorption. The catalytic activity was found to be dependent on the amount of ozone consumed and the dispersion and reducibility of MnOx on the catalyst surface.

Catalytic oxidation of benzene using mesoporous alpha-Mn2O3.

The catalytic oxidation of benzene was carried out over mesoporous alpha-Mn2O3, MnOx/KIT-6, and bulk commercial Mn oxides (Mn2O3, MnO2, and MnO). The catalysts were characterized using X-ray diffraction, X-ray photoelectron spectroscopy, Brunauer-Emmett-Teller analysis, and temperature-programmed reduction analysis. MnOx/KIT-6, prepared by impregnating MnOx on KIT-6, exhibited a low activity for the oxidation of benzene, whereas mesoporous alpha-Mn2O3, manufactured using KIT-6 as the template, showed a high activity. The order of the activities of bulk Mn oxides for benzene decomposition was shown to be Mn2O3 > MnO2 > MnO. Therefore, the high activity of mesoporous alpha-Mn2O3 is attributed to the uniform distribution of highly active Mn2O3 in the mesoporous structure.

Preparation of monolithic cu(In0.7Ga0.3)Se2 nanopowders and subsequent fabrication of sintered CIGS films.

Cu(In,Ga)Se2 (CIGS) is a compound semiconductor and is one of the most attractive light-absorbing materials for use in thin film solar cells. Among the various approaches to prepare CIGS thin films, the powder process offers an extremely simple and materials-efficient method. Here, we report the mechano-chemical preparation of CIGS compound powders suitable for fabrication of CIGS films by a powder process. We found that the CIGS phase was formed from the elemental powders of Cu, In, and Se and liquid Ga using high energy milling process with a milling time as short as 40 min at 200 rpm due to a self-accelerating exothermic reaction. The morphology and size of the CIGS powders changed with a function of the milling speed (100-300 rpm), leading to an optimal condition of milling at 200 rpm for 120 min. We also found that it was difficult to obtain a monolithic phase of the CIGS powders without severe particle aggregation by mechano-chemical milling alone. Therefore, in combination with the milling, subsequent heat-treatment at 300 degrees C was performed, which successfully provided monolithic CIGS nanopowders suitable for powder process. When a thin film was fabricated from the monolithic CIGS nanopowders, a highly dense film with large crystalline grains was obtained. The CIGS film preserved its chemical composition of CuIn0.7Ga0.3Se2 after sintering as evidenced by Raman spectroscopy, EDS and SAED pattern of transmission electron microscopy. The film was also found suitable for a light absorbing layer of CIGS solar cells with its band gap energy of 1.14 eV evaluated by transmittance spectroscopy.

Detection and characterization of nanomaterials released in low concentrations during multi-walled carbon nanotube spraying process in a cleanroom.

Release of nanomaterials was assessed in a cleanroom workplace designed for the handling of multi-walled carbon nanotubes. During the process, the nanotubes were sprayed in a chamber fitted with an exhaust duct system. The front door of the spraying chamber was completely closed, but rear end of the chamber was partially open. Throughout a series of spray processes, three detectors - an optical particle counter, a nanoparticle aerosol monitor, and an aethalometer - counted and characterized particles escaping the chamber. Concentrations of particle surface area and black carbon emitted by the spraying were assessed assuming zero background aerosol concentration in the cleanroom. Very low concentrations of black carbon, 0.4 µg/m(3), were observed. In conclusion, in a cleanroom, low concentrations of nanomaterials were detected to be emitted from a spraying chamber into the workplace. The level of particles reaching the workplace was sufficiently low to have made their detection difficult in a normal environment. Both target nanomaterial and non-intended incidental nanomaterials were released during spraying. Despite the use of exhaust duct system in the process chamber, workers would be exposed to some particles if the chamber were partially open. The exhaust duct system was not enough to remove all the particles released in the chamber.

Airborne estimation of SO2 emissions rates from a coal-fired power plant using two top-down methods: A mass balance model and Gaussian footprint approach.

In this study, two top-down methods-mass balance and Gaussian footprint-were used to determine SO2 emissions rates via three airborne sampling studies over Korea's largest coal power plant in October 2019 and 2020. During the first two flights in October 2019, mass balance approaches significantly underestimated the SO2 emissions rates by 75 % and 28 %, respectively, as obtained from the real-time stack monitoring system. Notably, this large discrepancy accounted for the insufficient number of transects altitudes and high levels of background SO2 along the upwind side. Alternatively, the estimated SO2 emissions rates of the third flight (October 2020) displayed a difference of <10 % from rea-time monitoring data (630 vs. 690 kg·hr-1), owing to the enhanced vertical resolution with increased transects and lower background SO2 levels. In contrast to the mass balance method, Gaussian footprints offered significantly improved accuracy (relative error: 41 %, 32 %, and 2 % for Flights 1, 2, and 3, respectively). This relatively good performance was attributed to prior emissions knowledge via the Clean Air Policy Support System (CAPSS) emissions inventory and its unique ability to accurately estimate stack-level SO2 emissions rates. Theoretically, the Gaussian footprint was less prone to sparse transects and upwind background levels. However, it can be substantially influenced by atmospheric stability and consequently by effective stack heights and dispersion parameters; basically, all factors with minimal-to-no influence on the mass balance approach. Conversely, the mass balance method was the only plausible approach to estimate unidentified source emissions rates when well-defined prior emission information was unknown. Here, the footprint approach supplemented the mass balance method when the emission inventories were known, and employing both strategies approaches greatly enhanced the integrity of top-down emissions inventories from the power plant sources, thus, supporting their potential for ensuring operational compliance with SO2 emissions regulation.

Comparison of the sources and oxidative potential of PM2.5 during winter time in large cities in China and South Korea.

Regional air pollution is rising in Northeast Asia due to increasing energy consumption resulting from a growing population and intensifying industrialization. This study analyzes the sources of air pollution using fine particulate matter (PM2.5) sampling from the atmosphere over Korea and China. We then use this analysis to further investigate the relationship between organic compounds (source tracers) and the oxidative potential of PM2.5. The PM2.5 concentration during winter measured at a measurement stations in Korea showed no significant variation year-to-year. The PM2.5 concentrations measured during winter at a site near Beijing, China were 62.45 µg/m3 in 2018 and 33.07 µg/m3 in 2020. The sources, as determined from PMF, were analyzed at a site in Korea, the sources as secondary nitrate (34.10 %), secondary sulfate (20.20 %), coal combustion (4.01 %), vehicle emission (8.55 %), cooking and biomass burning (18.39 %), dust (8.45 %), and SOA (6.29 %) were identified. At a site in China, secondary nitrate (17.54 %), secondary sulfate (12.03 %), coal combustion (15.53 %), vehicle emission (12.43 %), cooking and biomass burning (9.25 %), dust (26.40 %), secondary organic aerosol (6.82 %) were identified. Our results show secondary organic carbon had a positive association with oxidative potential in Korea while primary organic carbon presented higher correlation with oxidative potential in China. Further, the ECMWF Reanalysis v5 (ERA5) wind field during the high PM2.5 events demonstrated airflow from the west coast of China resulting in high polar organic compounds at the Korean monitoring site. The results further support that aged PM2.5, which contains secondary products, leads to increased oxidative potential. The results presented explain the high concentrations of secondary products and the impact on the biological activities of PM2.5, supporting additional actions to address the impacts of long-range transport of PM2.5.

Catalytic oxidation of benzene with ozone over nanoporous Mn/MCM-48 catalyst.

The catalytic oxidation of a representative volatile organic compound, benzene, with ozone at a low temperature was investigated. A nanoporous MCM-48 material with a high specific surface area was used as the support for the catalytic oxidation for the first time. Mn, which has high activity at a low temperature, was used as the metal catalyst. To examine the effect of the Mn precursor, MCM-48 was impregnated with two different Mn precursors: Mn acetate and Mn nitrate. The characteristics of the synthesized catalysts were analyzed by Brunauer Emmett Teller surface area, X-ray diffraction, X-ray photoelectron spectroscopy, and temperature-programmed reduction. MCM-48 impregnated with Mn acetate showed higher catalytic activity than MCM-48 impregnated with Mn nitrate. This result was attributed to the better dispersion within nanoporous MCM-48 and higher oxygen mobility of Mn oxides produced by Mn acetate. The catalytic activity was also shown to depend closely on the ozone concentration.

Preparation of airborne Ag/CNT hybrid nanoparticles using an aerosol process and their application to antimicrobial air filtration.

Carbon nanotubes (CNTs) have been widely used in a variety of applications because of their unique structure and excellent mechanical and electrical properties. Additionally, silver (Ag) nanoparticles exhibit broad-spectrum biocidal activity toward many different bacteria, fungi, and viruses. In this study, we prepared Ag-coated CNT hybrid nanoparticles (Ag/CNTs) using aerosol nebulization and thermal evaporation/condensation processes and tested their usefulness for antimicrobial air filtration. Droplets were generated from a CNT suspension using a six-jet collison nebulizer, passed through a diffusion dryer to remove moisture, and entered a thermal tube furnace where silver nanoparticles were generated by thermal evaporation/condensation at ∼980 °C in a nitrogen atmosphere. The CNT and Ag nanoparticle aerosols mixed together and attached to each other, forming Ag/CNTs. For physicochemical characterization, the Ag/CNTs were introduced into a scanning mobility particle sizer (SMPS) for size distribution measurements and were sampled by the nanoparticle sampler for morphological and elemental analyses. For antimicrobial air filtration applications, the airborne Ag/CNT particles generated were deposited continuously onto an air filter medium. Physical characteristics (fiber morphology, pressure drop, and filtration efficiency) and biological characteristics (antimicrobial tests against Staphylococcus epidermidis and Escherichia coli bioaerosols) were evaluated. Real-time SMPS and transmission electron microscopy (TEM) data showed that Ag nanoparticles that were <20 nm in diameter were homogeneously dispersed and adhered strongly to the CNT surfaces. Because of the attachment of Ag nanoparticles onto the CNT surfaces, the total particle surface area concentration measured by a nanoparticle surface area monitor (NSAM) was lower than the summation of each Ag nanoparticle and CNT generated. When Ag/CNTs were deposited on the surface of an air filter medium, the antimicrobial activity against test bacterial bioaerosols was enhanced, compared with the deposition of CNTs or Ag nanoparticles alone, whereas the filter pressure drop and bioaerosol filtration efficiency were similar to those of CNT deposition only. At a residence time of 2 h, the relative microbial viabilities of gram-positive S. epidermidis were ∼32, 13, 5, and 0.9% on the control, CNT-, Ag nanoparticle-, and Ag/CNT-deposited filters, respectively, and those of gram-negative E. coli were 13, 2.1, 0.4, and 0.1% on the control, CNTs, Ag nanoparticles, and Ag/CNTs, respectively. These Ag/CNT hybrid nanoparticles may be useful for applications in biomedical devices and antibacterial control systems.

Effect of Mn precursors on benzene oxidation with ozone over MnOx/MCM-41 at low temperature.

Low temperature benzene oxidation in the presence of ozone on MnOx/MCM-41 catalysts has been studied. MnOx/MCM-41 catalysts were prepared from two different precursors, Mn(NO3)2 and Mn(CH3COO)2, and these samples were characterized by N2 sorption, X-ray diffraction, X-ray photoelectron spectroscopy and temperature programmed reduction. The characterization results showed that the MnOx/MCM-41 prepared from Mn(CH3COO)2 had higher oxygen mobility and dispersion than the MnOx/MCM-41 from Mn(NO3)2. As a result, the MnOx/MCM-41 obtained from Mn(CH3COO)2 showed higher catalytic activity for the oxidation of benzene using ozone; however, without ozone, the catalytic activity was negligible.

Electrospray-assisted ultraviolet aerodynamic particle sizer spectrometer for real-time characterization of bacterial particles.

The ultraviolet aerodynamic particle sizer (UVAPS) spectrometer is a novel, commercially available aerosol counter for real-time, continuous monitoring of viable bioaerosols based on the fluorescence induced from living microorganisms. For aerosolization of liquid-based microorganisms, general aerosolization methods such as atomization or nebulization may not be adequate for an accurate and quantitative characterization of the microorganisms because of the formation of agglomerated particles. In such cases, biological electrospray techniques have an advantage because they generate nonagglomerated particles, attributable to the repulsive electrical forces among particles with unipolar charges. Biological electrosprays are quickly gaining potential for the detection and control of living organisms in applications ranging from mass spectrometry to developmental microbiology. In this study, we investigated the size distribution, total concentration, and fluorescence percentage of bacterial particles in a real-time manner by electrospray-assisted UVAPS. A suspension containing Escherichia coli as a test microorganism was sprayed in a steady cone-jet mode using a specially designed electrospray system with a point-to-orifice-plate configuration based on charge-reduced electrospray size spectrometry. With the electrospray process, 98% of the total E. coli particle number concentration had a size of <1 mum and the geometric mean diameter was 0.779 mum, as compared with the respective values of 78% and 0.907 mum after nebulization. The fractions of fluorescence responsive particles and of particles that contained viable organisms in culture were 12% and 7%, respectively, from the electrospray process and 34% and 24% from nebulization. These results demonstrate that (1) the presence of agglomerated particles can lead to markedly overestimated fluorescence and culturability percentages compared with the values obtained from nonagglomerated particles, and (2) electrospray-assisted UVAPS can provide more accurate and quantitative real-time characterization of liquid-based microorganisms, owing to the generation of nonagglomerated particles.

Exposure assessment of carbon nanotube manufacturing workplaces.

Seven CNT (carbon nanotube) handling workplaces were investigated for exposure assessment. Personal sampling, area sampling, and real-time monitoring using an SMPS (scanning mobility particle sizer), dust monitor, and aethalometer were performed to characterize the mass exposure, particle size distribution, and particle number exposure. No workplace was found to exceed the current ACGIH (American Conference of Governmental Industrial Hygienists) TLVs (threshold limit values) and OELs (occupational exposure levels) set by the Korean Ministry of Labor for carbon black (3.5 mg/m(3)), PNOS (particles not otherwise specified; 3 mg/m(3)), and asbestos (0.1 fiber/cc). Nanoparticles and fine particles were most frequently released after opening the CVD (chemical vapor deposition) cover, followed by catalyst preparation. Other work processes that prompted nanoparticle release included spraying, CNT preparation, ultrasonic dispersion, wafer heating, and opening the water bath cover. All these operation processes could be effectively controlled with the implementation of exposure mitigation, such as engineering control, except at one workplace where only natural ventilation was used.

Monitoring multiwalled carbon nanotube exposure in carbon nanotube research facility.

With the increased production and widespread use of multiwalled carbon nanotubes (MWCNTs), human and environmental exposure to MWCNTs is inevitably increasing. Therefore, this study monitored the possible exposure to MWCNT release in a carbon nanotube research laboratory. To estimate the potential exposure of researchers and evaluate the improvement of the workplace environment after the implementation of protective control measures, personal and area monitoring were conducted in an MWCNT research facility where the researchers handled unrefined materials. The number, composition, and aspect ratio of MWCNTs were measured using scanning transmission electron microscopy with an energy-dispersive x-ray analyzer. The gravimetric concentrations of total dust before any control measures ranged from 0.21 to 0.43 mg/m(3), then decreased to a nondetectable level after implementing the control measures. The number of MWCNTs in the samples obtained from the MWCNT blending laboratory ranged from 172.9 to 193.6 MWCNTs/cc before the control measures, and decreased to 0.018-0.05 MWCNTs/cc after the protective improvements. The real-time monitoring of aerosol particles provided a signature of the MWCNTs released from the blending equipment in laboratory C. In particular, the number size response of an aerodynamic particle sizer with a relatively high concentration in the range of 2 to 3 microm in aerodynamic diameter revealed the evidence of MWCNT exposure. The black carbon mass concentration also increased significantly during the MWCNT release process. Therefore, the present study suggests that the conventional industrial hygiene measures can significantly reduce exposure to airborne MWCNTs and other particulate materials in a nano research facility.

Inactivation of S. epidermidis, B. subtilis, and E. coli bacteria bioaerosols deposited on a filter utilizing airborne silver nanoparticles.

In the present study, a control methodology utilizing airborne silver nanoparticles is suggested and tested with respect to its potential to control Gram-positive Staphylococcus epidermidis and Bacillus subtilis, and Gram-negative Escherichia coli bacteria bioaerosols deposited on filters. As it is known that the Gram-negative bacteria are sensitive to airflow exposure, the main focus of this study for testing the airborne silver nanoparticles effect was the Gram-positive Staphylococcus epidermidis and Bacillus subtilis bacteria bioaerosols whereas Escherichia coli bioaerosols were utilized for comparison. Airborne bacteria and airborne silver nanoparticles were quantitatively generated in an experimental system. Bioaerosols deposited on the filter were exposed to airborne silver nanoparticles. The physical and biological properties of the airborne bacteria and airborne silver nanoparticles were measured via aerosol measurement devices. From the experimental results, it was demonstrated that this method utilizing airborne silver nanoparticles offers potential as a bioaerosol control methodology.