A Probability Model for Evaluating Building Contamination from an Environmental Event

ABSTRACT

Asbestos dust and bioaerosol sampling data from suspected contaminated zones in buildings allowed development of an environmental data evaluation protocol based on the differences in frequency of detection of a target contaminant between zones of comparison. Under the assumption that the two test zones of comparison are similar, application of population proportion probability calculates the significance of observed differences in contaminant levels. This was used to determine whether levels of asbestos dust contamination detected after a fire were likely the result of smoke-borne contamination, or were caused by pre-existing/background conditions.

Bioaerosol sampling from several sites was also used to develop the population proportion probability protocol. In this case, significant differences in indoor air contamination relative to the ambient conditions were identified that were consistent with the visual observations of contamination. Implicit in this type of probability analysis is a definition of “contamination” based on significant differences in contaminant levels relative to a control zone. Detection of a suspect contaminant can be assessed as to possible sources(s) as well as the contribution made by pre-existing (i.e., background) conditions, provided the test and control zones are subjected to the same sampling and analytical methods.     

An Investigation of Odors and Volatile Organic Compounds Released during Composting

ABSTRACT

The emissions of odors and volatile organic compounds produced from a commercial composting operation have been studied using a laboratory-scale composting system. The composting activity of a typical commercial compost feed was followed by monitoring the composting temperature, as well as the respiratory rate. Using a controlled aeration system, the gaseous volatiles produced were tested for odors using the "dilution-to-threshold" method, as well as gas composition, as determined by gas chromatography-mass spectrometry.

The results indicated that while there may be a reasonable correlation between the release of volatile organic compounds (VOCs) and odors, care has to be taken when trying to identify offensive odors with specific chemical species. However, the data obtained suggests that offensive odors formed during commercial composting may be due to sulfurous and nitrogenous compounds, although their concentrations in the compost gases may not be very high.

The major release of VOCs occurred during the first two weeks of composting, after which the gaseous releases fell dramatically as the composting process proceeded and temperatures started to fall.     

Impact of Indoor Environmental Parameters on Formaldehyde Concentrations in Unoccupied Research Houses

An environmental parameters study has examined the impact of indoor temperature (T) and relative humidity (RH) levels on formaldehyde (CH₂O) concentrations inside two unoccupied research houses where the primary CH₂O emitter is particleboard underlayment. The data were fit to a simple three-term, steady state model describing the T and RH dependence of CH₂O concentration in a single compartment with a single CH₂O emitter. The model incorporates an Arrhenius T dependence and a nonlinear RH dependence of the CH₂O vapor concentration within the solid CH₂O emitter. The RH dependence is based on Freundlich's theory of the adsorption of water vapor on solid surfaces. The model is used to estimate potential seasonal variation in CH₂O concentrations under specified experimental conditions inside the research houses. The modeled results indicate six- to ninefold variation between 18°C, 20% RH and 32°C, 80% RH, simulating potential winter/summer conditions with minimal indoor climate control. In comparison, Indoor conditions ranging from 20°C, 30% RH to 26°C, 60% RH yielded approximate two- to fourfold fluctuations in CH₂O concentration.

The research house data were also used to evaluate the limitations and applicability of more complex five-term models developed from small-scale chamber studies of the environmental dependence of CH₂O emissions from particleboard underlayment. These models also incorporate a linear T and RH dependence of the CH₂O transport rate through the CH₂O emitter in addition to the T and RH dependence of the CH₂O concentration within the emitter. Good correlation is observed between the results of the research house studies and 1) a selected (i.e., single) underlayment model over a broad range of environmental conditions and 2) a combined underlayment model over a restricted range of environmental conditions.     

Assessment of Arsenic Losses during Ashing: A Comparison of Two Methods Applied to Atmospheric Participates

A comparison was made of over 300 pairs of arsenic results from instrumental neutron activation and flameless atomic absorption analyses of atmospheric particulates collected on glass fiber filters. Atomic absorption analyses involved low temperature ashing of filters at high power levels. No matrix modification chemicals were added to the acid extract which was analyzed. Neutron activation results are on the average 9% higher than those obtained by atomic absorption and the difference is statistically significant. This small difference is probably due to the analytical techniques or acid extraction and not in any important way to losses during low temperature ashing. This conclusion is in sharp contrast to other recently reported situations where low temperature ashing losses in analyzing atmospheric particulate were sizable. Although the atmospheres sampled differed somewhat between these situations the most obvious difference was in the combustibility of the filters used in sampling.     

A Sampling Protocol for Composting,Recycling, and Re-use of Municipal Solid Waste

Abstract

This article reports on development of a protocol for characterizing municipal solid waste (MSW). This protocol is similar to that recommended by the American Society for Testing and Materials but includes a distinction between pure and mixed loads of MSW. Thirteen component categories were used with a focus on material feed stock for composting, recycling, and reuse. The required number of samples was determined to achieve a 80%, 90%, and 95% statistical accuracy for characterizing MSW categories at 1% and 2% sampling error. This study found that a maximum of 25 randomly collected samples of 200 pounds will reflect each component category of mixed load MSW with at least a 95% confidence level and 2% error. This protocol was successfully tested in Monongalia County, West Virginia, to provide a “snapshot” MSW characterization during early summer.     

Tube-Immunoassay for Rapid Detection of Carbaryl Residues in Agricultural Products

An antibody-based rapid, quantitative, and qualitative tube enzyme-linked immunosorbent assay (tube-ELISA) was developed and used to determine carbaryl (1-naphthyl methylcarbamate) residues in agricultural products (apple, Chinese cabbage, rice, and barley). The tube-ELISA is a competitive immunoassay in which the antibody is coated in the polystyrene tube, with a dynamic range between 0.7 and 46.3 μg kg^?1. Carbaryl was extracted from each agricultural sample by hand-shaking with methanol and examined for application to on-site analysis. After the liquid extraction, the sample extracts diluted with buffer were analyzed by rapid tube-ELISA directly. The overall test time was around 15–30 min, including sample preparation and assay performance. The results obtained from tube-ELISA correlated well with high-performance liquid chromatography (R ² > 0.9). The study shows that tube-ELISA is useful as a quality control tool and can be used to quantitatively detect carbaryl as well.     

Estimation of Efficiency of Processing Soil Samples for Pesticide Residues Analysis

The efficiency of four sample processing methods was tested with eight different types of soils representing the major proportion of cultivated soils. The principle of sampling constant was applied for characterizing the efficiency of the procedures and testing the well-mixed status of the prepared soil. The test material was 14C-labeled atrazine that enabled keeping the random error of analyses ≤ about 1%. Adding water to the soil proved to be the most efficient and generally applicable procedure resulting in about 6% relative sample processing uncertainty for 20 g test portions. The expected error is inversely proportional to the mass of test portion. Smashing and manual mixing of soil resulted in about four times higher uncertainty than mixing with water. Grinding of soil is applicable for dry soils only, but the test procedure applied was not suitable for estimating a typical uncertainty of processing dry soil samples. Adding dry ice did not improve the efficiency of sample processing.     

Environmental release of dioxins from reservoir sources during beach nourishment programs

In late 1990s, USEPA/FDA made an important connection regarding the presence of elevated levels of dioxins (e.g., 1500 ng kg⁻¹ TEQ) in ball clays mined in Mississippi (USA) from a geological deposit dated to ∼40 million years (Mississippi Embayment) that stretches over several states (northern part of Mississippi to Kentucky) and levels of dioxins in selected animal food sources. Following a recent beach nourishment program along the mid-Atlantic coast of the US, a number of dark gray, blue tinted nuggets of varying sizes were found on beach strands and near the shoreline. Using the presence of these balls of clay (shape, color, and knowledge regarding their use in pottery) on the beach, together with our direct experience analyzing ball clays for dioxins, we made a possible association between these clays and elevated dioxins. Concerns regarding the potential of nourishment programs to cause severe damage to our beaches drove us to test the dioxin content of nourishment exposed clays. A number of the nuggets, along with freshly dredged and deposited sand (collected the morning after nourishment) with the same coloration, and others (sun-bleached), collected approximately 2 weeks after the completion of the nourishment efforts, were analyzed for the presence of PCDD/Fs, PCBs, and selected semi-volatile chlorinated organics. The clay PCDD/F WHO2005-TEQs (dry weight; ND = DL; EMPC = EMPC) ranged from 0.41 to 5.78 ng kg⁻¹ with an average of 2.64 ng kg⁻¹, whereas the sand sample’s TEQs ranged from 0.18 to 0.31 ng kg⁻¹ PCDD/F WHO-2005, with an average of 0.22 ng kg⁻¹. The average total tetra- through octachlorinated dibenzo-p-dioxin concentration was 2700 ng kg⁻¹ (with a maximum of 5800 ng kg⁻¹) for the clays and 8.5 ng kg⁻¹ (with a maximum of 16.8 ng kg⁻¹) for the sand samples. The congener 2,3,7,8-TCDD (TEF = 1) was detected in half of the clay samples (0.11-0.77 ng kg⁻¹). All of the clay and sand samples displayed an unambiguous and dominating 1,4,6,9-chlorination pattern across homolog groups. No other chlorinated aromatics were detected above background levels. The observations, along with the absence or an extremely low level of polychlorinated dibenzofurans, together with the mineralogical analysis, supports the conclusion that off-shore dredging activities are reaching reservoir sources containing dioxin-tainted, smectic/kaolinite clay minerals. Subsequent beach erosion provides additional environmental releases over time, as buried balls of clay from previous nourishment efforts become exposed.     

Evaluating the ability of a numerical weather prediction model to forecast tracer concentrations during ETEX 2

In this paper the meteorological processes responsible for transporting tracer during the second ETEX (European Tracer EXperiment) release are determined using the UK Met Office Unified Model (UM). The UM predicted distribution of tracer is also compared with observations from the ETEX campaign. The dominant meteorological process is a warm conveyor belt which transports large amounts of tracer away from the surface up to a height of 4 km over a 36 h period. Convection is also an important process, transporting tracer to heights of up to 8 km. Potential sources of error when using an operational numerical weather prediction model to forecast air quality are also investigated. These potential sources of error include model dynamics, model resolution and model physics. In the UM a semi-Lagrangian monotonic advection scheme is used with cubic polynomial interpolation. This can predict unrealistic negative values of tracer which are subsequently set to zero, and hence results in an overprediction of tracer concentrations. In order to conserve mass in the UM tracer simulations it was necessary to include a flux corrected transport method. Model resolution can also affect the accuracy of predicted tracer distributions. Low resolution simulations (50 km grid length) were unable to resolve a change in wind direction observed during ETEX 2, this led to an error in the transport direction and hence an error in tracer distribution. High resolution simulations (12 km grid length) captured the change in wind direction and hence produced a tracer distribution that compared better with the observations. The representation of convective mixing was found to have a large effect on the vertical transport of tracer. Turning off the convective mixing parameterisation in the UM significantly reduced the vertical transport of tracer. Finally, air quality forecasts were found to be sensitive to the timing of synoptic scale features. Errors in the position of the cold front relative to the tracer release location of only 1 h resulted in changes in the predicted tracer concentrations that were of the same order of magnitude as the absolute tracer concentrations.     

A New Instrument for Evaluating the Visual Quality of Air

Any device for assessing the visual quality of air must necessarily have an extremely high sensitivity since, at times, the Rayleigh scattering of air molecules is the determining factor. The integrating nephel-ometer of Brewer and Beuttell has been adapted for air quality measurement. It records the volume scattering coefficient and was reliable in over a month of continuous operation. The results may be interpreted in terms of visual range; if so the inherent noise in the system corresponds to more than 500 miles visual range with a 100-second response time. The low cost, simplicity, and sensitivity of the device make it appear useful for rapid evaluation of visual air quality. The design of the instrument will be presented, including both the optical and electronic components. The results of operation of the instrument in Seattle during days of moderate air pollution will be used to illustrate the utility of the device.     

Environmental impacts of the widespread use of chlorine-based disinfectants during the COVID-19 pandemic

Environmental Science and Pollution Research - Chlorinated disinfectants are widely used in hospitals, COVID-19 quarantine facilities, households, institutes, and public areas to combat the spread...     

Evaluating the use of occupational standards for controlling toxic air pollutants

Currently, the U.S. Environmental Protection Agency has established air standards for relatively few chemicals. As a result, state agencies are faced with controlling air contaminants for a large number of chemicals posing potential public health threats. Use of occupational standards as a basis for deriving ambient air guidelines is a method used by states to control air toxics. This standard development approach is reviewed by considering the differences in the health basis and numerical values which often occur among the occupational standards set by OSHA, NIOSH and ACGIH. This study indicated that careful selection should be made of the most appropriate occupational standard to use to protect public health. A comparison is made of chemicals regulated by various state air toxic programs using occupational standards lowered by a safety factor to concentrations established by the U.S. EPA. It was found that the air guidelines vary, but the degree of stringency can be comparable.     

A Framework for Risk Characterization of Environmental Pollutants

Risk characterization is defined by both the U.S. National Academy of Sciences and the U.S. EPA as the estimation of human health risk due to harmful (i.e., toxic or carcinogenic) substances or organisms. Risk characterization studies are accomplished by integrating quantitative exposure estimates and dose-response relationships with the qualitative results of hazard identification.

A Risk Characterization Framework has been developed to encourage a systematic approach for analysis and presentation of risk estimates. This methodology subdivides the four common components of the risk assessment process into ten elements. Each of these elements is based on a term in a predictive risk equation. The equation allows independent computations of exposure, dose, lifetime individual risk, and risk to affected populations. All key assumptions in the predictive risk equation can be explicitly shown. This is important to understand the basis and inherent uncertainties of the risk estimation process.

The systematic treatment of each of the ten elements in this framework aids in the difficult job of comparing risk estimates by different researchers using different methodologies. The Risk Characterization Framework has been applied to various indoor and outdoor air pollutants of a carcinogenic nature. With further development, it also promises to be applicable to noncarcinogenic effects.     

Evaluating the cytotoxicity of palladium/magnetite nano-catalysts intended for wastewater treatment

Palladium/magnetite nanoparticulate catalysts were developed for efficient elimination of halogenated organic pollutants from contaminated wastewater. Particle recovery from treated water can be ensured via magnetic separation. However, in worst-case scenarios, this catalyst removal step might fail, leading to particle release into the environment. Therefore, a toxicological study was conducted to investigate the impact of both pure magnetite and palladium/magnetite nanoparticle exposure upon human skin (HaCaT) and human colon (CaCo-2) cell lines and a cell line from rainbow trout gills (RTgill-W1). To quantify cell viability after particle exposure, three endpoints were examined for all tested cell lines. Additionally, the formation of reactive oxygen species was studied for the human cells. The results showed only minor effects of the particles on the tested cell systems and support the assumption that palladium/magnetite nano-catalysts can be implemented for a new wastewater treatment technology in which advantageous catalyst properties outweigh the risks.     

An Evaluation of the Kriging Method to Predict 7-h Seasonal Mean Ozone Concentrations for Estimating Crop Losses

Using kriging, a statistical technique, the National Crop Loss Assessment Network (NCLAN) program estimated growing season 5-month (May-September) ambient 7-h mean O₃ concentrations for each of the major crop growing areas of the United States for 1978-1982. The O₃ estimates were used to predict economic benefits anticipated by lowering O₃ levels in the United States. This paper reviews NCLAN’s use of kriging to estimate 7-h seasonal mean O₃ concentrations for crop growing regions. Although the original kriging program used by NCLAN incorrectly calculated the diagonal elements of the kriging equations, this omission did not result in significant errors in the predicted estimates. Most of the data used in estimating the 7-h seasonal values were obtained from urban areas; the use of these data tended to underestimate the 7-h seasonal O₃ concentrations in rural areas. It is recommended that only O₃ data that are representative of agricultural areas and have been collected under accepted quality assurance programs be used In future kriging efforts.     

Environmental fate and bioavailability of agent orange and its associated dioxin during the vietnam war

BACKGROUND: In 1996, the Committee on the Assessment of Wartime Exposure to Herbicides in Vietnam of the National Academy of Sciences' Institute of Medicine (IOM) issued a report on an exposure model for use in epidemiological studies of Vietnam veterans. This exposure model would consider troop locations based on military records; aerial spray mission data; estimated ground spraying activity; estimated exposure opportunity factors; military indications for herbicide use; and considerations of the composition and environmental fate of herbicides, including changes in the TCDD content of the herbicides over time, the persistence of TCDD and herbicides in the environment, and the degree of likely penetration of the herbicides into the ground. When the final report of the IOM Committee was released in October 2003, several components of the exposure model envisioned by the Committee were not addressed. These components included the environmental fate of the herbicides, including changes in the TCDD content over time, the persistence of TCDD and herbicides in the environment, and the degree of likely penetration of herbicides into the ground. This paper is intended to help investigators understand better the fate and transport of herbicides and TCDD from spray missions, particularly in performing epidemiological studies. METHODS: This paper reviews the published scientific literature related to the environmental fate of Agent Orange and the contaminant, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), and discusses how this affected the potential exposure to TCDD of ground troops in Vietnam. Specifically, the mechanisms of dissipation and degradation as they relate to environmental distribution and bioavailability are addressed. RESULTS: The evaluation of the spray systems used to disseminate herbicides in Vietnam showed that they were capable of highly precise applications both in terms of concentrations sprayed and area treated. Research on tropical forest canopies with leaf area indices (a measure of foliage density) from 2 to 5 indicated that the amount of herbicide and associated TCDD reaching the forest floor would have been between 1 and 6% of the total aerial spray. Studies of the properties of plant surface waxes of the cuticle layer suggested that Agent Orange, including the TCDD, would have dried (i.e., be absorbed into the wax layer of the plant cuticle) upon spraying within minutes and could not be physically dislodged. Studies of Agent Orange and the associated TCDD on both leaf and soil surface have demonstrated that photolysis by sunlight would have rapidly decreased the concentration of TCDD, and this process continued in shade. Studies of 'dislodgeable foliar residues' (DFR, the fraction of a substance that is available for cutaneous uptake from the plant leaves) showed that only 8% of the DFR was present 1 hr after application. This dropped to 1% of the total 24 hrs after application. Studies with human volunteers confirmed that after 2 hrs of saturated contact with bare skin, only 0.15-0.46% of 2,4,5-T, one of the phenoxy acetic acid compounds that was an active ingredient of Agent Orange, entered the body and was eliminated in the urine. CONCLUSIONS: The prospect of exposure to TCDD from Agent Orange in ground troops in Vietnam seems unlikely in light of the environmental dissipation of TCDD, little bioavailability, and the properties of the herbicides and circumstances of application that occurred. Photochemical degradation of TCDD and limited bioavailability of any residual TCDD present in soil or on vegetation suggest that dioxin concentrations in ground troops who served in Vietnam would have been small and indistinguishable from background levels even if they had been in recently treated areas. Laboratory and field data reported in the literature provide compelling evidence on the fate and dislodgeability of herbicide and TCDD in the environment. This evidence of the environmental fate and poor bioavailability of TCDD from Agent Orange is consistent with the observation of little or no exposure in the veterans who served in Vietnam. Appreciable accumulation of TCDD in veterans would have required repeated long-term direct skin contact of the type experienced by United States (US) Air Force RANCH HAND and US Army Chemical Corps personnel who handled or otherwise had direct contact with liquid herbicide, not from incidental exposure under field conditions where Agent Orange had been sprayed.     

Preparation of Activated Carbons from Raw and Biotreated Agricultural Residues for Removal of Volatile Organic Compounds

ABSTRACT

Activated carbons with diverse physical and chemical properties were produced from four agriculture residues, including raw barley husk, biotreated barley husk, rice husk, and pistachio shell. Results showed that with adequate steam activation (30–90 min, 50% H₂O_(g)/50% N₂), activated carbons with surface areas between 360 and 950 m² g^?1 were developed. Further increases in the activation time destroyed the pore structure of activated carbons, which resulted in a decrease in the surface area and pore volume. Biotreated agricultural residues were found to be suitable precursors for producing mesoporous activated carbons. The oxygen content of activated carbons increased with increasing activation time. Results from X-ray photoelectron spectroscopy examination further suggested that H₂O molecules react with the carbon surface, enhancing the deconvoluted peak area of carbonyl and carboxyl groups. Equilibrium adsorption of toluene indicated that the adsorption capacities increased with an increase in the inlet toluene concentration and a decrease in temperature. The adsorption isotherms were successfully fitted with Freundlich, Langmuir, and Dubinin– Radushkevich equations. Activated carbons derived from agricultural residues appear to be more applicable to adsorb volatile organic compounds at a low concentration and high-temperature environment.

IMPLICATIONS This paper presents data on the preparation of activated carbons from agricultural residues, especially the waste from biohydrogen generation. Experimental results indicated that with proper carbonization and steam activation, activated carbons with diverse characteristics can be produced from various agricultural residues. The resulting activated carbons effectively adsorb toluene. This work provides useful information for reutilization of these agricultural residues, helping in decreasing the cost of biological waste treatment and providing a cost-effective alternative to conventional adsorbent production and application.