An experimental study of air entrainment and oxygen transfer at a water jet from a nozzle with air holes.

An adequate supply of dissolved oxygen is important in natural rivers and in some water treatment processes. The dissolved oxygen concentration can be enhanced by entraining air bubbles in a receiving pool. When a water jet impinges a receiving pool at rest, air bubbles may be entrained and carried away below the pool free surface. This process is called plunging water jet entrainment and aeration. This paper describes an experimental study of the air entrainment rate and oxygen transfer efficiency of circular nozzles with and without air holes. In particular, the effect of varying the number, positions, and open/close status of the air holes is investigated. A negative pressure occurred depending on the air holes opened on the circular nozzles. This phenomenon affected the water jet expansion, water jet shape, air entrainment, and bubble penetration depth and, hence, the oxygen transfer efficiency. It was demonstrated that the air entrainment rate and the oxygen transfer efficiency of the circular nozzles with air holes were better than those of the circular nozzles without air holes. Therefore, adding air holes to a simple, circular nozzle could lead to a significantly increased air entrainment rate and oxygen transfer efficiency.     

Aerosol formation yields from the reaction of catechol with ozone

The formation of secondary organic aerosol from the gas-phase reaction of catechol (1,2-dihydroxybenzene) with ozone has been studied in two smog chambers. Aerosol production was monitored using a scanning mobility particle sizer and loss of the precursor was determined by gas chromatography and infrared spectroscopy, whilst ozone concentrations were measured using a UV photometric analyzer. The overall organic aerosol yield (Y) was determined as the ratio of the suspended aerosol mass corrected for wall losses (M_o) to the total reacted catechol concentrations, assuming a particle density of 1.4 g cm^?3. Analysis of the data clearly shows that Y is a strong function of M_o and that secondary organic aerosol formation can be expressed by a one-product gas–particle partitioning absorption model. The aerosol formation is affected by the initial catechol concentration, which leads to aerosol yields ranging from 17% to 86%. The results of this work are compared to similar studies reported in the literature.     

Aerosol light scattering measurements as a function of relative humidity

The hygroscopic nature of atmospheric fine aerosol was investigated at a rural site in the Great Smoky Mountains National Park during July and August 1995. Passing the sample aerosol through an inlet, which housed an array of Perma Pure diffusion dryers, controlled the sample aerosol's relative humidity (RH). After conditioning the aerosol sample in the inlet, the light scattering coefficient and the aerosol size distribution were simultaneously measured. During this study, the conditioned aerosol's humidity ranged between 5% < RH < 95%. Aerosol response curves were produced using the ratio bspw/bspd; where bspw is the scattering coefficient measured at some RH greater than 20% and bspd is the scattering coefficient of the "dry" aerosol. For this work, any sample RH values below 15% were considered dry. Results of this investigation showed that the light scattering ratio increased continuously and smoothly over the entire range of relative humidity. The magnitude of the ratio at a particular RH value, however, varied considerably in time, particularly for RH values greater than approximately 60%. Curves of the scattering coefficient ratios as a function of RH were generated for each day and compared to the average 12-hour chemical composition of the aerosol. This comparison showed that for any particular RH value the ratio was highest during time periods of high sulfate concentrations and lowest during time periods of high soil or high organic carbon concentrations.     

Design and Operating Parameters for a Large Ambient Aerosol Chamber

Recent investigations of ambient aerosol behavior over urban areas have pointed out the need for controlled experimental data to link together field investigation results and computer simulation studies. This paper describes the design considerations, construction details and operating parameters of a large (8000 ft³) outside reaction chamber constructed in rural North Carolina. The chamber is triangular in cross-section, 20 ft wide, 20 ft high and 40 ft long, and is covered with clear 5 ml Teflon film. The outdoor location of the chamber permits the reaction volume to be exposed to the natural conditions of temperature and solar radiation. A recirculating air system allows the air in the chamber to be passed through an “absolute” fiberglas filter for adjustment of condensation nuclei concentration and also through driers for humidity adjustment. Internal fans are provided for mixing of the chamber contents without use of the recirculating system so that various degrees of turbulence can be approximated. A sampling line from the chamber passes directly to an instrument room, located directly under the chamber, where direct analyses for particle composition, concentration, and size, and gas composition and concentration are carried out. Parameters which can be varied in this system include number, size, distribution, and chemical composition of pre-existing nuclei, as well as humidity, solar radiation, temperature, and trace gas concentration and composition.     

Aerosol speciation and mass prediction from toluene oxidation under high NOx conditions

A kinetically based gas-particle partitioning box model is used to highlight the importance of parameter representation in the prediction of secondary organic aerosol (SOA) formation following the photo-oxidation of toluene. The model is initialized using experimental data from York University's indoor smog chamber and provides a prediction of the total aerosol yield and speciation. A series of model sensitivity experiments were performed to study the aerosol speciation and mass prediction under high NO_x conditions (VOC/NO_x = 0.2). Sensitivity experiments indicate vapour pressure estimation to be a large area of weakness in predicting aerosol mass, creating an average total error range of 70 μg m^?3 (range of 5–145 μg m^?3), using two different estimation methods. Aerosol speciation proved relatively insensitive to changes in vapour pressure. One species, 3-methyl-6-nitro-catechol, dominated the aerosol phase regardless of the vapour pressure parameterization used and comprised 73–88% of the aerosol by mass. The dominance is associated with the large concentration of 3-methyl-6-nitro-catechol in the gas-phase. The high NO_x initial conditions of this study suggests that the predominance of 3-methyl-6-nitro-catechol likely results from the cresol-forming branch in the Master Chemical Mechanism taking a significant role in secondary organic aerosol formation under high NO_x conditions. Further research into the yields and speciation leading to this reaction product is recommended.     

Phosphorus quantity-intensity relationships and agronomic measures of P in surface layers of soil from a long-term slurry experiment

Soils from a long-term slurry experiment established in 1970 at Hillsborough, Northern Ireland, were used in the experiment. The site has a clay loam soil overlying Silurian shale. Seven treatments were used with three replicate plots per treatment. Control plots were treated with mineral fertiliser supplying 200 kg N, 32 kg P and 160 kg K ha(-1) yr(-1). Slurry treatment plots were in two blocks and treated with either pig or cow slurry supplied at 50, 100 or 200 m3 ha(-1) yr(-1). Agronomic measures of P determined on 10-cm soil cores were compared with measured P quantity/intensity (Q/I) parameters from fitted sorption and desorption isotherms. Phosphorus affinity constant was found to be significantly and negatively correlated with P loading of soils. Desorption rate coefficient also increased significantly with increase in P loading from slurry, although there was no significant difference between slurry types (cow vs. pig). In contrast, while agronomic measures of P (water-soluble P, Olsen P, calcium chloride-extractable P, degree of P saturation (DPS)) also correlated significantly with P loading and total P (TP) in the soils, there was a separation and significant differences between the cow and pig slurry treatment blocks, with the former being much lower. Phosphorus inputs to pig slurry treated plots were much higher than to equivalent cow slurry plots over the first 15 years of the study but declined sharply over the most recent 10 years to more or less par. Conventional measures of agronomic P such as Olsen P and DPS, measure only P accumulation over the longer term and indicated only the higher content of P accumulating in soil of pig slurry treatments. Risk of P loss estimated by Q/I parameters appeared to show very similar behaviour between the two slurry types in line with more recent manurial additions but in contradiction of P accumulation statistics.     

Variability of parameters measured during the resuspension of sediments with a particle entrainment simulator

The release of contaminants from sediments is an important problem facing environmental managers concerned with issues such as maintenance dredging, habitat restoration and dredge spoil placement. While there are laboratory methods to assess the remobilization of contaminants from resuspended sediments, little is known about how their operating characteristics influence a sediments response to resuspension. In this study, a particle entrainment simulator (PES) for resuspending sediments was evaluated by assessing variability among replicates and over operation time (12 h) for three estuarine sediments. These sediments varied in physical and chemical properties as well as the degree of metal contamination. Results showed that under identical resuspension conditions, there was low variability among sediment replicates. Sediment properties and the degree of metal contamination affected the magnitude and variation in water column parameters and contaminant release. Fine-grained sediments affected water column parameters, which stabilized over several hours of resuspension. While metal concentrations in the aqueous and particulate samples varied throughout operation, variation was highest for Cd and Ni. Compared to other methods used to evaluate the effects of sediment resuspension, the PES has operational advantages such as the ability to monitor water column conditions and resuspend sediment at specified energy levels. Overall, the PES provided reproducible conditions of resuspension effects among sediments varying in composition and contamination, demonstrating its value as a tool to evaluate contaminant mobility.     

Use of an inverse dispersion technique for estimating ammonia emission from surface-applied slurry

Ammonia (NH₃) emission from land application of manure is typically measured using the integrated horizontal flux (IHF) micrometeorological method. However, there are some situations in which alternative techniques (such as an inverse dispersion modelling technique) might be preferable, for example when measuring from large or irregularly shaped source areas. In this study, an inverse dispersion technique using the backward Lagrangian stochastic (bLS) model, with 2 different experimental configurations, was compared with the Integrated Horizontal Flux method (i.e. IHF), which was used as reference technique. Pig slurry was surface-applied at 125 kg N ha^?1 to bare soil on a large plot (80 × 125 m). Cumulative emissions were 19.3, 21.2 and 18.4 kg N ha^?1 from the IHF and the bLS technique (experimental configurations I and II), respectively. Mean flux within each sampling period as estimated by the two techniques compared extremely well, with a slope not significantly different from 1 and r² of 0.99. Although limited in extent, this dataset agree with a previous study in demonstrating the use of the bLS technique with longer period time-averaged concentration measurements.     

Electrical Measurement of the Mass Concentration of a Self-Preserving Aerosol Size Distribution

Recently fifty-eight measurements of urban aerosol size distributions by Clark have shown that these distributions agree quite well with the self preserving form proposed by Friedlander within the size range of 0.05 to 5 microns radius. This paper shows that for an aerosol obeying the self preserving distribution model, the volume concentration (and, hence, the mass concentration for constant density) is directly proportional to the electric current collected when the aerosol is unipolarly charged, passed through a weak electric field to remove particles smaller than 0.05 micron and then collected by a current collector. It is shown that the linear relation between the mass concentration and collected current is independent of the unipolar charging method used. A test of this theory using Clark’s electric counter data was encouraging and suggests that the electric measurement of urban aerosol mass concentrations by properly designed instruments may be feasible.     

Design and Testing of a New Size Classifying Isokinetic Sequential Aerosol Sampler

Two versions of a size-classifying isokinetic sequential aerosol sampler (SCISAS) have been designed, built, tested, and deployed in a field program in the southwestern United States. The SCISAS units can operate at unattended sites, exposing four or more filter types simultaneously, in two size ranges, for six sampling time Intervals. Design considerations included theoretical estimates of aerosol particle losses in the 0-15 μm size range.

SCISAS prototypes have been tested to evaluate their sampling efficiency as a function of flow rate, the sensitivity of the sampling efficiency to isokinetic matching within the SCISAS sampling stack, the equivalency of their sampling ports, and their passive deposition characteristics. The prototypes were also compared to several other types of aerosol filtration samplers already in common use. These tests show that particle loss mechanisms within the SCISAS usually cause no more than 5 percent losses, and that the SCISAS units agree, within one to two measurement uncertainty intervals, with other types of aerosol samplers.     

Aerosol analysis by field desorption mass spectrometry combined with a new sampling technique

Analyses of inorganic and organic aerosols by Field Desorption Mass Spectrometry at high resolution are presented in this article. The method is unique in giving direct semi-quantitative information on intact inorganic salts, as they are present in the sample. Airborn polar organic compounds are also readily detected. Due to the high sensitivity of the method, sub-microgram quantities are sufficient for an analysis. Aerosols can therefore be collected by direct impaction on the field emitter which is subsequently transferred into the mass spectrometer. Advantages of this procedure are its relative simplicity and rapidity, providing information complementary to established methods of aerosols analysis.     

Mathematical modelling of flue-gas desulphurisation using lime slurry in a turbulent contact absorber

A mathematical model has been developed for absorption of SO₂ from flue gases using lime slurry in Turbulent Contact Absorbers (TCA). In this model, the TCA was simulated by considering it as a falling film absorption system. Turbulent effects were taken into account by using eddy viscosity and eddy diffusivity. The system of partial differential equations of mass transfer with moving boundaries was solved numerically in order to obtain the concentration profiles of the reactants, the thickness of the reaction zone and the outlet gas concentration. A bench-scale TCA was built up, and the mathematical model was evaluated against experimental data obtained from the built device. The model predictions showed good agreement with the experimental data and literature data.     

Temporal characteristics from continuous measurements of PM2.5 and speciation at the Taipei Aerosol Supersite from 2002 to 2008

This study uses monitoring data collected at the Taipei Aerosol Supersite from March 2002 to February 2008 to analyze characteristics such as seasonal fluctuations, diurnal variations, and photochemical-related variations of PM_2.5 chemical compositions. The results indicate that the average of PM_2.5 mass concentration in Taipei during this period is 30.3 ± 16.0 μg m^?3. The highest average concentration of PM_2.5 components is that of sulfate, which accounts for 21.1% of the PM_2.5 mass, followed by organic carbon (OC) at 15.9%, nitrate at 5.8%, and elemental carbon (EC) at 5.4%. Concentrations of EC, OC, and nitrate have distinctive but similar seasonal fluctuations, which is highest in spring and lowest in fall. Sulfate concentration has less seasonal fluctuations, and the highest value appears during the fall. Similarly, concentrations of EC, OC, and nitrate have notable diurnal variations; however, the diurnal variation of sulfate concentration is not very apparent. These observation data show that EC, OC, and nitrate in PM_2.5 in the Taipei metropolis come mainly from local emissions, while sulfate comes mainly from the regional transport of pollutants. This is likely because Taiwan is located on the lee zone of the Asian prevailing winds from fall to spring; its air quality is frequently affected by the transport of air pollutants from Mainland China. In addition, the extent of increase in aerosols is much higher than that of CO, indicating the formation of secondary aerosol when photochemical activity is strong. Based on six years of observation data, this study explores three potential scenarios to set up Taiwan's PM_2.5 air quality standard (AQS). The analysis indicates that the optimum standard for 24-h air quality of PM_2.5 should be around 50 μg m^?3.     

Remobilization of polycyclic aromatic hydrocarbons during the resuspension of Yangtze River sediments using a particle entrainment simulator

Remobilization of 16 polycyclic aromatic hydrocarbons (PAHs) during sediment resuspension was investigated using a particle entrainment simulator at shear stress from 0.2 to 0.5Nm(-2), typical of the energy levels present in many tidally driven aquatic environments. The results suggested that desorption from the entrained particles was the primary source of dissolved PAHs. summation operatorPAHs concentrations in particles on volume normalization increased about four times. However, on mass weight basis, summation operatorPAHs concentrations decreased from 6039.74+/-138.28microgkg(-1) to 1665.39+/-112.26microgkg(-1). The same trend was observed for individual PAHs. Dissolved concentrations of PAHs demonstrated significant differences depending on molecular weight and applied shear. The distribution of PAHs between particle and water phase suggested that for three-ring PAHs, the amounts of PAHs in particles were higher than the predicted values during our experiments. This might be due to presence of another active sorbent.     

Emissions of ammonia, hydrogen sulfide, and odor before, during, and after slurry removal from a deep-pit swine finisher

It is a common practice in the midwestern United States to raise swine in buildings with under-floor slurry storage systems designed to store manure for up to one year. These so-called "deep-pit" systems are a concentrated source for the emissions of ammonia (NH3), hydrogen sulfide (H2S), and odors. As part of a larger six-state research effort (U.S. Department of Agriculture-Initiative for Future Agriculture and Food Systems Project, "Aerial Pollutant Emissions from Confined Animal Buildings"), realtime NH3 and H2S with incremental odor emission data were collected for two annual slurry removal events. For this study, two 1000-head deep-pit swine finishing facilities in central Iowa were monitored with one-year storage of slurry maintained in a 2.4 m-deep concrete pit (or holding tank) below the animal-occupied zone. Results show that the H2S emission, measured during four independent slurry removal events over two years, increased by an average of 61.9 times relative to the before-removal H2S emission levels. This increase persisted during the agitation process of the slurry that on average occurred over an 8-hr time period. At the conclusion of slurry agitation, the H2S emission decreased by an average of 10.4 times the before-removal emission level. NH3 emission during agitation increased by an average of 4.6 times the before-removal emission level and increased by an average of 1.5 times the before-removal emission level after slurry removal was completed. Odor emission increased by a factor of 3.4 times the before-removal odor emission level and decreased after the slurry-removal event by a factor of 5.6 times the before-removal emission level. The results indicate that maintaining an adequate barn ventilation rate regardless of animal comfort demand is essential to keeping gas levels inside the barn below hazardous levels.     

Nutrient removal from biogas slurry and biogas upgrading by microalgae-fungi-bacteria co-cultivation under different carbon nanotubes concentration

In this study, Chlorella vulgaris, Ganoderma lucidum, and endophytic bacteria were co-cultivated with the stimulation of strigolactone analogs GR24 to prepare pellets. During the purification of biogas slurry and biogas, multi-walled carbon nanotubes (MWCNTs) were introduced to enhance the removal efficiencies of nutrients and CO₂. The results showed that both GR24 and MWCNTs affected the purification of biogas slurry and biogas. The maximum chemical oxygen demand, total nitrogen, total phosphorus, and CO₂ removal efficiencies of the Chlorella vulgaris-Ganoderma lucidum-endophytic bacterial symbionts were 82.57 ± 7.96% (P < 0.05), 82.14 ± 7.87% (P < 0.05), 84.27 ± 7.96% (P < 0.05), and 63.93 ± 6.22% (P < 0.05), respectively, with the induction of 10⁻⁹ M GR24 and 1 mg L⁻¹ MWCNTs. Moreover, the growth and photosynthetic performance of the symbionts were consistent with the removal effects. The Chlorella vulgaris-Ganoderma lucidum-endophytic bacterial symbionts obtained high growth rates and enzyme activity with the maximum growth rate of 0.365 ± 0.03 d⁻¹, mean daily productivity of 0.182 ± 0.016 g L⁻¹ d⁻¹, and carbonic anhydrase activity of 31.07 ± 2.75 units, respectively. These results indicated that an appropriate concentration of GR24 and MWCNTs could promote the growth of symbionts, reinforce the purification effects of biogas slurry and biogas, and provide a new idea for the simultaneous purification of wastewater and biogas.

     

Degradation of 2,4,6-trinitrotoluene in water and soil slurry utilizing a calcium peroxide compound

The degradation of 2,4,6-trinitrotoluene was examined in pure water and contaminated soil slurry using calcium peroxide as a source of solid hydrogen peroxide and oxygen. The extent of TNT oxidation was compared with that obtained by using hydrated lime, which is normally generated by slurrying CaO2 in water and contained in CaO2 technical formulation (approximately 50%, w/w). Complete TNT degradation occurred between 280 min, 0.1% CaO2/Ca(OH)2 and 20 min, 1% CaO2/Ca(OH)2. A large part of the generated oxidation products, 80-90%, were absorbed on the solid calcium hydroxide, whereas the remaining 10-20% was detected in solution until 48 h. Removal of nitro groups was extremely effective in CaO2 slurry, where all the nitrogen (3 mol per mol of TNT) was removed from TNT within 240 min. Respect to calcium hydroxide, the peroxy compound liberated H2O2 in solution, 370 mg l-1 at 0.2% CaO2, w/v, which then decomposed within 480 min. Most of the 14C-TNT was retained more strongly on the calcium hydroxide generated by slurrying CaO2. This pool remained adsorbed on the solid until pH dropped below 5.8. The treatment of a contaminated soil slurry, 700 mg TNT kg-1, reduced CH3CN extractable TNT below 20 mg kg-1 at very low concentration of CaO2/Ca(OH)2, approximately 0.2%, w/w. Both oxidants do not lead to soil sterilization as the phosphorus added to neutralize the pH serves as a source of nutrient for the soil biomass.     

Aerosol laser ablation mass spectrometry of suspended powders from PM sources and its implications to receptor modeling

Primary sources of particulate matter (PM) were analyzed by suspending powdered samples into an aerosol laser ablation mass spectrometer (LAMS). PM sources studied included vehicle exhaust particulates, dust from a non-ferrous smelter, cement powder, incinerator fly ash, two coal fly ash samples, and two soils. Marker peaks signified certain PM source sectors: construction particles could be distinguished by abundant Ca and Ca compounds, fuel combustion was marked by elemental carbon clusters, and nonferrous industrial particles showed inorganic As, Cu, Pb, Zn, and SOx. In addition to the distinction between particles from these different source sectors, mass spectral results also showed that for a single source, different particle types existed, and among different sources within a sector, similar spectra were present. The aerosol LAMS results show the difficulty in differentiating among separate fly ash sources as well as among different soil samples. A particle class balance receptor model that measures the amount of specific particle types rather than the amount of a chemical component is suggested as a means of source apportionment when particle spectra with overlapping source possibilities occur. The assumptions and limitations of receptor modeling aerosol LAMS data are also described. In particular, methods need to be developed to account for the contribution of secondary sources.