A novel bipolar charger for submicron aerosol particles using carbon fiber ionizers

A simple and novel bipolar charging device using carbon fiber ionizers was developed to neutralize submicron aerosol particles without the generation of ozone. The ion currents of the positive and negative ions generated by carbon fiber ionizers were so chosen as to optimize particle neutralization. The particle penetration, charging probability and charge distribution resulting from the charger were investigated and compared to those from a Kr-85 radioactive neutralizer for the particles in the size range of 20–120 nm. Size distributions for various laboratory-generated aerosols (sodium chloride, ammonium nitrate, ammonium sulfate and glutaric acid) neutralized by the charger were also investigated and compared to those obtained without neutralization. Particle penetration in the charger was over 90% for particles larger than 20 nm. Charging probability and charge distribution for the charger were in good agreement with those from Kr-85 neutralizer and with theoretical estimations. Size distributions observed for the charger and Kr-85 neutralizer were also in good agreement for particles of different concentrations and various chemical compositions. The newly developed bipolar carbon fiber charger can neutralize submicron particles, at least as effectively as currently available radioactive neutralizers and with negligible ozone generation which is its major advantage.     

Preparation of stable cross-linked enzyme aggregates (CLEAs) of NADH-dependent nitrate reductase and its use for silver nanoparticle synthesis from silver nitrate

The NADH-dependent nitrate reductase from Fusarium oxysporum cell extract was directly immobilized as cross linked enzyme aggregates (CLEAs) and investigated for the synthesis of silver nanoparticles by a reduction of silver nitrate. The effects of precipitant type and cross-linking on activity recovery of enzyme in CLEAs were studied. After aggregation of enzyme with ammonium sulfate followed by cross-linking formed aggregates for 4 h with 8 mM glutaraldehyde, 93% activity recovery was achieved in CLEAs with enhanced thermal stability at 50 °C and 40 °C. Scanning electron microscopy analysis showed that immobilized NADH-dependent nitrate reductase was of spherical structure. CLEAs showed 90% catalytic yield even after 4 cycles of repeated use in silver nanoparticle synthesis at pH 7.2 and temperature 35 °C.     

Abundance and size distribution of HULIS in ambient aerosols at a rural site in South China

HUmic-LIke Substances (HULIS) comprise a significant fraction of the water-soluble organic aerosol mass and influence the water uptake properties of aerosols in the atmosphere. In this work, the abundance and size distributions of HULIS in ambient aerosols were measured in a rural location in South China at a time with a visible presence of crop residue burning. PM_2.5 samples of fresh smoke from burning rice straw and sugar cane leaves were also collected and analyzed for HULIS and major aerosol constituents. HULIS were abundant in both ambient samples and in fresh biomass burning emissions, accounting for ～60% of the water-soluble organic carbon in the ambient aerosols and ～30% in the fresh biomass burning aerosols. In the particles in the range of 0.32–1.8 μm, the abundance of HULIS was 40–90% of the combined abundance of sulfate and ammonium, suggesting that HULIS should be considered when quantifying the role of sulfate aerosols serving as cloud condensation nuclei. The size distribution of HULIS was characterized by a dominant droplet mode with a mass median aerodynamic diameter (MMAD) in the range of 0.63–0.87 μm, accounting for 81% of the total HULIS mass, a minor condensation mode (12%, MMAD: 0.23–0.28 μm) and a coarse mode (7%, MMAD: 4.0–5.7 μm). The small amount of HULIS in the coarse mode indicated that soil-derived HULIS was a very minor source. On the basis of the size distribution characteristics, HULIS were postulated to have multiple sources, including secondary formation in cloud droplets, secondary formation through heterogeneous reactions or aerosol-phase reactions, and primary emissions from biomass burning.     

Regional modeling of secondary organic aerosol over China using WRF/Chem

Using a new generation air quality modeling system (WRF/Chem) fully coupled with secondary organic aerosol model (SORGAM), we investigate the spatial and temporal characteristics of secondary organic aerosol (SOA) as well as the relative contributions of anthropogenic and biogenic sources to the formation of SOA in 2006 over China. To improve SOA simulation, a parameterization scheme for the isoprene induced SOA formation was added in WRF/Chem. The simulated SOA concentrations show large temporal and spatial variability, with the highest levels occur in summer and the lowest concentrations occur in winter. The high SOA regions are located near 30°N in central China in summer, with values exceeding 8 μg m^?3, while they shift to South China, mainly in Pearl River Delta (PRD) region in winter, with the concentrations at or below 2 μg m^?3. Across the whole country, the average ground level SOA concentrations are 0.94, 2.54, 1.41, 0.43, and 1.34 μg m^?3 in spring, summer, autumn, winter, and year, respectively. Commonly, the SOA loading is mostly concentrated in the boundary layer (～70%). Although the SOA concentrations are dominated by biogenic sources in summer, the contributions of anthropogenic sources exceed biogenic sources over most areas in winter. On the national level, the anthropogenic sources contribute 35% of total SOA, with 41%, 26%, 39%, and 59% in spring, summer, autumn and winter, respectively. The estimated annual SOA production reaches 3.05 Tg yr^?1 over China, accounting for about 4–25% of global SOA formation. The modeled OC and EC concentrations as well as SOC to OC ratios are compared with the measurements and previous studies. The results suggest that the spatial and temporal characteristic of OC and EC levels is well captured by the model. However, the simulated SOA concentrations in this study might be underestimated by 0–75%. The modeling SOA in this paper are in agreement with other field and modeling studies, also showing the importance of SOA in total organic aerosol in China.     

A study of the scaling height of the tropospheric aerosol and its extinction coefficient profile

A method is proposed to determine a so-called scaling height of the tropospheric aerosol and the exponent-type aerosol extinction coefficient profile from the pyrheliometer or sunphotometer measurements and surface visibility data. Using the method, characteristics of seasonally/yearly mean scaling heights and aerosol extinction profiles over 11 sites in China during 1994–2001 are analyzed. The yearly-mean scaling heights over the 11 sites change between 1.30 and 2.67 km, and they are very variable for different seasons, being usually larger in spring. As far as the yearly-mean scaling heights of all 11 sites are concerned, they change between 1.88 and 2.11 km during 1994–2001, having an increasing trend. The scaling heights from pyrheliometer data are compared with those from AERONET sunphotometer data, and a good agreement between them is obtained.     

A miniature disk electrostatic aerosol classifier (mini-disk EAC) for personal nanoparticle sizers

We have developed a miniature disk electrostatic aerosol classifier (mini-disk EAC) for use in electrical mobility-based personal nanoparticle instrumentation for measurement of personal exposures to nanoaerosols. The prototype consists of two parallel disk electrodes separated by an electrically insulating spacer, to create the particle classification zone. The aerosol enters and exits the classification zone along the bottom disk electrode. An additional, particle-free sheath flow is used to improve the measurement resolution. The transmission measurement of the mini-disk EAC for DMA-classified particles shows that particle losses due to diffusion and electrical image forces were low. The particle penetration at 10 nm diameter (the designed lower size limit for the classifier) was 67% when the prototype was operated at the aerosol and sheath flow rates of 0.5 and 1.0 l min^?1, respectively. The performance of the mini-disk EAC was experimentally characterized using the particle cutoff curves that describe their penetration through the classifier as a function of applied voltage across the two disk electrodes. Based on the measurement of particle penetration at different aerosol and sheath flows, it was found that the aerosol and sheath flow rates of 0.5 and 1.5 l min^?1 were optimal for classifier operation. Finally, a semi-empirical model was also developed to describe the transfer function of the mini-disk EAC for non-diffusive particles.     

A STUDY OF PROCESSES THAT GOVERN THE MAINTENANCE OF AEROSOLS IN THE MARINE BOUNDARY LAYER

We systematically evaluate the relative influence of sources and sinks of particles in the remote marine boundary layer (MBL) to elucidate the principal factors that govern MBL aerosol behavior. Processes considered include: (1) surface flux of dimethyl sulfide (DMS); (2) gas-phase oxidation of DMS to SO₂; (3) gas-phase oxidation of SO₂ to H₂SO₄; (4) mass transfer of SO₂ and H₂SO₄ to pre-existing particles; (5) homogenous nucleation of H₂SO₄/H₂O; (6) entrainment of air from the free troposphere; (7) deposition to the sea surface; (8) cycling of air through clouds and rain scavenging; (9) oxidation of SO₂ in sea salt aerosols and cloud droplets; and (10) sea-salt particle production at sea surface. The average aerosol number concentration is found to be quite sensitive to the rate of entrainment of aerosol-containing air from the free troposphere. The path that leads to the greatest accumulation of non-sea-salt (nss) sulfate involves SO₂ (rather than H₂SO₄) absorption into existing particles. Because of scavenging of SO₂ and H₂SO₄ by sea-salt aerosol, a considerable fraction of nss-sulfate is internally mixed with sea-salt aerosol. Under the conditions assumed in this study, MBL aerosol number concentration is dominated by free tropospheric aerosol under virtually all conditions, 89% in the base case, and even 69% at a 17 m s^-1 wind speed. Aerosol mass, on the other hand, is dominated by sea-salt particles, 62% in the base case and 98% at a wind speed of 17 m s^-1. Evaporation of cloud droplets provides 4.6% of the particle number in the base case, but 28% of the particle mass. At the high nucleation rate case considered here, there is notably little change in the overall contributions to aerosol number and mass from the base case; only about 5% of the total particle number is provided by nucleation events. Variation in precipitation frequency also has only a minor effect on the overall contributions. One concludes that the MBL aerosol is remarkably robust in the face of ever-changing conditions. Free tropospheric aerosol entrainment tends to sustain particle number concentrations, and sea-salt emissions maintain most of the aerosol mass. Cloud processing, while not a major contributor to aerosol number, does provide, except under high wind conditions, the order of 20% of the aerosol mass. Although nucleation occurs only infrequently and does not contribute appreciably to long-term average aerosol number or mass, nucleation is, nonetheless, the mechanism that replenishes aerosol number in brief, intense episodes when aerosol surface area levels are substantially reduced by precipitation.     

Au and Cu recovery from printed boards by decomposition of epoxy resin in supercritical water

The recovery of Au and Cu from a printed board using supercritical water was studied, and the effects of the treatment with and without an oxidant on the components of the printed board were compared.Over 99 wt.% of metallic Au and metallic Cu was recovered in the solid form by oxidant-free supercritical water treatment at 400 °C and 25 MPa. However, the maximal removal of solid organics was 70 wt.% due to char-generation. Promotion of hydrolysis and inhibition of char-generation enhanced the removal of solid organics to nearly 90 wt.% at 380 °C.Under oxidative conditions, complete separation of solid organics from the inorganics occurred within 60 min. Metallic Au was unaltered and successfully recovered. Over 90 wt.% of metallic Cu was oxidized within 5 min, and only Cu oxides were recovered after 30 min. Oxidation of organics was promoted by coexisting Cu compounds contained in the printed board.     

CFD simulations of enhanced condensational growth (ECG) applied to respiratory drug delivery with comparisons to in vitro data

Enhanced condensational growth (ECG) is a newly proposed concept for respiratory drug delivery in which a submicrometer aerosol is inhaled in combination with saturated or supersaturated water vapor. The initially small aerosol size provides for very low extrathoracic deposition, whereas condensation onto droplets in vivo results in size increase and improved lung retention. The objective of this study was to develop and evaluate a CFD model of ECG in a simple tubular geometry with direct comparisons to in vitro results. The length (29 cm) and diameter (2 cm) of the tubular geometry were representative of respiratory airways of an adult from the mouth to the first tracheobronchial bifurcation. At the model inlet, separate streams of humidified air (25, 30, and 39 °C) and submicrometer aerosol droplets with mass median aerodynamic diameters (MMADs) of 150, 560, and 900 nm were combined. The effects of condensation and droplet growth on water vapor concentrations and temperatures in the continuous phase (i.e., two-way coupling) were also considered. For an inlet saturated air temperature of 39 °C, the two-way coupled numerical (and in vitro) final aerosol MMADs for initial sizes of 150, 560, and 900 nm were 1.75 μm (vs. 1.23 μm), 2.58 μm (vs. 2.66 μm), and 2.65 μm (vs. 2.63 μm), respectively. By including the effects of two-way coupling in the model, agreements with the in vitro results were significantly improved compared with a one-way coupled assumption. Results indicated that both mass and thermal two-way coupling effects were important in the ECG process. Considering the initial aerosol sizes of 560 and 900 nm, the final sizes were most influenced by inlet saturated air temperature and aerosol number concentration and were not largely influenced by initial size. Considering the growth of submicrometer aerosols to above 2 μm at realistic number concentrations, ECG may be an effective respiratory drug delivery approach for minimizing mouth–throat deposition and maximizing aerosol retention in a safe and simple manner. However, future studies are needed to explore effects of in vivo boundary conditions, more realistic respiratory geometries, and transient breathing.     

Optimizing endopectinase production from date pomace by Aspergillus niger PC5 using response surface methodology

In the first stage of experiments, a two-level fractional factorial design was used for screening of the most important factors among concentration of ammonium sulfate, potassium dihydrogen phosphate and date pomace, pH, total spore amount, aeration rate and fermentation time for the production of endopectinase from date pomace by Aspergillus niger PC5. Based on the results of first stage, ammonium sulfate (0.25–0.45%), pH (4.82–6.12) and fermentation time (50–90 h) were selected to be studied further. In the second stage, response surface methodology was used to determine the optimum fermentation conditions for production of the enzyme. Second stage results showed that, fermentation time was the most significant factor on endopectinase activity. After modeling of the fermentation process, maximum amounts of endopectinase (10.88 U ml^?1) predicted to be in the following fermentation conditions: pH of medium 5, ammonium sulfate concentration of 0.3% and fermentation time of 76.05 h.     

Hybrid carbon source for single-walled carbon nanotube synthesis by aerosol CVD method

The conductivity enhancement of single-walled carbon nanotube (SWCNT) films was achieved by increasing the bundle length in an aerosol CVD synthesis method with the help of two carbon sources. Carbon monoxide provides carbon at temperatures below 900 °C, while ethylene takes over at higher temperatures. The significant decrease in the sheet resistance at the 90% transmittance was observed from 3500 to 7500 Ω/sq. for pure CO system via 1909 and 1709 Ω/sq. for CO–H₂ system to 291 and 358 Ω/sq. in the presence of C₂H₄ at 900 and 1100 °C, respectively. Doping the film with a gold chloride solution in acetonitrile allowed us to create the transparent conductive films with the sheet resistance as low as 73 Ω/sq. at a transmittance of 90%.     

Colossal permittivity in (In1/2Nb1/2)xTi1−xO2 ceramics prepared by a glycine nitrate process

(In + Nb) co-doped TiO₂ nanoparticles with very low dopant concentrations were prepared using a glycine nitrate process. A pure rutile—TiO₂ phase with a dense microstructure and homogeneous dispersion of dopants was achieved. By doping TiO₂ with 1.5% (In + Nb) ions, a very high dielectric permittivity of ε′ = 42,376 and low loss tangents of tanδ = 0.06 (at room temperature) were achieved. The large conduction activation energy at the grain boundary decreased with decreasing dopant concentration. The colossal permittivity was primarily attributed to the internal barrier layer capacitor (IBLC) effect. The dominant effect of interfacial polarization at the non–Ohmic sample–electrode contact was observed when the dopant concentration was ≤1.0 mol%. Interestingly, the sample–electrode contact and resistive–outer surface layer effects, i.e., surface barrier layer capacitor (SBLC) effect, has also an effect on the colossal dielectric response in (In + Nb) co-doped TiO₂ ceramics.     

Effect of Temperature on Phase and Alumina Extraction Efficiency of the Product from Sintering Coal Fly Ash with Ammonium Sulfate

A new developed technology for extracting alumina from coal fly ash was studied in this paper. In this technology, coal fly ash is first sintered with ammonium sulfate, forming ammonium aluminum sulfate in the resultant product, where alumina can be easily leached without using any strong acid or alkali. The products obtained under different sintering conditions were characterized by X-ray diffractometry. Alumina extraction efficiency of these products was also investigated. The results show that the sintering temperature and time substantially influence the phase composition and alumina extraction efficiency of sintered products, while the heating rate has little influence. The optimal sintering condition is 400 °C for 3 h in air with a heating rate of 6 °C·min^− 1. Under the optimal sintering condition, the alumina extraction efficiency from as-sintered coal fly ash can reach 85% or more.     

Experimental measurements and computational modeling of aerosol deposition in the Carleton-Civic standardized human nasal cavity

Aerosol deposition in the novel, “Carleton-Civic” standardized geometry of the human nasal cavity was studied both numerically and experimentally. Inhalation flow rates varied from 30 to 90 L/min in the experiments, and aerosol droplets had diameters ranging from 1.71 to 9.14 μm (impaction parameters ranging from 123.3 to 2527.6 μm L/min). For the numerical simulations, both the RANS/EIM (Reynolds averaged Navier–Stokes equations for the gas phase and eddy-interaction random walk models for the particulate phase) and large eddy simulations were used. The mechanism of aerosol deposition in the standardized nasal cavity was dominated by inertial impaction. Deposition data from the standardized nasal cavity transected cited in vitro data based on individual subjects. The data also correlated very well with cited in vivo measurements but generally showed less aerosol deposition for a given value of the impaction parameter. Regional deposition characteristics within the nasal passages were also investigated both experimentally and numerically and new trends of regional deposition versus impaction parameter are discussed. These trends provide new insight into the general deposition behaviour of various sized aerosols within the human nasal cavity.     

Chemical characterisation of marine aerosol at Amsterdam Island during the austral summer of 2006–2007

Atmospheric aerosols were collected in separate fine (<2.5 μm) and coarse (>2.5 μm) size fractions in the period December 2006–March 2007 at Amsterdam Island in the southern Indian Ocean. A major objective of the study was to assess biogenic impact on the marine aerosol. The samples were analysed for organic carbon, water-soluble organic carbon, major inorganic ionic species, and organic species, including methanesulphonate (MSA), dicarboxylic acids, and organosulphates. The concentrations of sea salt, non-sea-salt sulphate, and water-soluble and water-insoluble organic matter (WSOM and WIOM) were estimated. Sea salt dominated the composition of the aerosol and accounted for 83% and 91% of the sum of the mass of the four aerosol types in the fine and coarse size fractions, respectively. WSOM, which can serve as a proxy for biogenic secondary organic aerosol (SOA), accounted for only 2.8% of the sum of the mass of the four aerosol types in the fine size fraction. MSA was the dominating organic compound with a median concentration of 47 ng m^?3. The organosulphates were characterised as sulphate esters of hydroxyl acids and a dihydroxylaldehyde, which may originate from the oxidation of algal/bacterial unsaturated fatty acid residues. No evidence was found for isoprene SOA.     

Comparison of the operational characteristics between a nitrifying membrane bioreactor and a pre-denitrification membrane bioreactor process

A single submerged membrane bioreactor (MBR) for nitrification of ammonium and a pre-denitrification MBR process for total nitrogen (TN) removal were investigated in comparison. A single nitrifying MBR was fed with synthetic ammonium wastewater of up to 900 mgN/l without organics so that the MBR was maintained as a pure nitrifying system. A high nitrifying capacity around 1.8 kgNH₄-N/m³/day was achieved while keeping the ammonium oxidation rate above 98%. Sludge volume index (SVI) gradually decreased down to less than 50 indicating good settleability of nitrifying sludge. The increase of suction pressure was less than 5 cm Hg over 7-months of operation. TN removal efficiency was determined in a pre-denitrification configuration with an anoxic reactor. Synthetic wastewater of 1200 mgCOD/l and 200 mgN/l was fed to the system at loads of 2.4 kgCOD/m³/day and 0.4 kgN/m³/day, respectively. As the internal recycle ratio from aerobic to anoxic zone increased from 2 to 6, TN removal efficiency was enhanced from 70 ± 9 to 89 ± 3%. With the sludge concentration of around 12,000 mg/l, SVI was highly fluctuated from 60 to 350 indicating the partial deterioration of sludge settleability. The suction pressure after 8 months of operation increased to above 10 cm Hg which is higher than that in a single nitrifying MBR. The concentration of extracellular polymeric substances (EPS), especially for carbohydrate content, was higher in the operation of a pre-denitrification MBR process than in a single nitrifying MBR. It is likely that the sludge characteristic such as settleability is related with membrane fouling but, further extensive study is needed. The performance of a pre-denitrification MBR process was also verified with real petrochemical nitrogen wastewater.     

Three phase partitioning coupled with ultrasound for the extraction of ursolic acid and oleanolic acid from Ocimum sanctum

In this study, three phase partitioning (TPP) is coupled with ultrasound for the extraction of ursolic acid (UA) and oleanolic acid (OA) from Ocimum sanctum leaves and process has been optimized to obtain maximum recovery. TPP is a relatively novel bioseparation technique used for the extraction, concentration and purification of enzymes and natural products. The technique of TPP was explored for the extraction of ursolic acid (UA) and oleanolic acid (OA) from O. sanctum leaves. The influence of various process parameters (pH, ammonium sulfate saturation, crude extract to t-butanol ratio, time and feed loading) on the extraction efficiency was investigated to get highest yield. The optimized conditions were found to be as follows: time – 120 min, pH – 7, ammonium sulfate saturation – 50% w/v, crude extract to t-butanol ratio – 1:1 and feed loading – 7.5% w/v. The highest yield obtained for UA and OA was 79.48% and 80.67% respectively under optimized conditions of TPP. Compared with TPP higher yield (83.36% and 85.58%) was obtained by ultrasound assisted TPP (UATPP) at 40 kHz and 180 W power and the time required was only 14 min as compared to 120 min of TPP. The extraction yield obtained was also compared with conventional solvent extraction and TPP-ultrasound was found to be an attractive technique for the extraction of UA and OA from O. sanctum leaves.     

Slurry explosive detonation synthesis and characterization of 10 nm TiO2

TiO₂ was prepared by detonating a slurry explosive made of Ti precursor, ammonium nitrate, cyclotrimethylenetrinitramine (RDX), and polystyrene (EPS). X-ray diffraction, transmission electron microscopy, energy dispersive X-ray spectrometry, Fourier transform infrared spectroscopy, and UV–vis diffuse reflection spectroscopy revealed that the sample was composed of mixed crystals of rutile and anatase TiO₂ with irregular spherical shapes and 10 nm particle size. The minimum energy gap of the sample was 2.9 eV. An ideal TiO₂ explosive was prepared from a precursor/ammonium nitrate/RDX ratio of 1:1:0.6 and 2 g of EPS as a density modifier.     

Estimating black carbon aging time-scales with a particle-resolved aerosol model

Understanding the aging process of aerosol particles is important for assessing their chemical reactivity, cloud condensation nuclei activity, radiative properties and health impacts. In this study we investigate the aging of black carbon containing particles in an idealized urban plume using a new approach, the particle-resolved aerosol model PartMC-MOSAIC. We present a method to estimate aging time-scales using an aging criterion based on cloud condensation nuclei activation. The results show a separation into a daytime regime where condensation dominates and a nighttime regime where coagulation dominates. There is also a strong dependence on supersaturation threshold. For the chosen urban plume scenario and supersaturations ranging from 0.1% to 1%, the aging time-scales vary between 11 and 0.068 h during the day, and between 54 and 6.4 h during the night.