Identification and Quantitative Analysis of Particulate Air Contaminants by X-Ray Diffraction Spectrometry

Because of the synergistic effects which take place from the mixing of gases and particulates in ambient air, it is important that the determination of air contaminants be carried out on the sample in its native state without imposing any further chemical recombination during the analysis. Since x-ray diffraction provides a chemically passive method of analysis and yields molecular rather than elemental information, we have undertaken the siudy of, and have successfully employed crystal diffraction lines as a qualitative and quantitative means for determining such materials as lime, calcium carbonate, road salt, coke dust, and aerosol from sinter emissions as well as several other less common industrial particulates in samples obtained from dustfall as dispersed in a matrix of powdered amorphous glass. Correlative to the above investigation this method was also extended to the study of such gases as sulfur dioxide which may be selectively fixed to an active surface.     

Day-of-Week Patterns in Toxic Air Contaminants in Southern California

Abstract

Day-of-week mean ambient concentrations were computed for six high-cancer-risk toxic air contaminants (TACs): 1,3-butadiene, benzene, acetaldehyde, formalde-hyde, carbon tetrachloride (CCl₄), and perchloroethylene. Data from six urban sites in southern California, from 1989 through 2001, were analyzed. Graphical displays were used to search for repeated patterns. Benzene and 1,3-butadiene, emitted mainly by mobile sources, exhibit distinctly lower concentrations on Sundays and slightly lower concentrations on Saturdays and Wednesdays. Acetaldehyde and formaldehyde show some trace of a weekly pattern similar to that of benzene and 1,3-butadiene, but the pattern is not strongly marked. Perchloroethylene, used primarily as a dry-cleaning solvent, is also distinctly lower on Sundays. CCl₄ does not show a dayof-week pattern.     

Mathematical Model for Photocatalytic Destruction of Organic Contaminants in Air

Abstract

Photocatalytic oxidation (PCO) was investigated in a bench-scale reactor for the abatement of two airborne organic contaminants: toluene and ethanol. A mathematical model that includes the impacts of light intensity, initial contaminant concentration, catalyst thickness, and relative humidity (RH) on the degradation of organic contaminants in a photocatalytic reactor was developed to describe this process. The commercially available catalyst Degussa-PtTiO₂ was selected to compare with the MTU-PtTiO₂-350 catalyst, which was synthesized by the sol-gel process, platinized, and calcined at 350 °C. For toluene removal using the MTU-PtTiO₂-350 catalyst, the degradation rate increased with increases in light intensity from 0.2 to 2.2 mW/cm² and in catalyst thickness from 0.00037 to 0.00361 cm. However, further increases in light intensity and catalyst thickness had only slight effect on the toluene degradation rate. Increasing the initial concentration from 6.29 to 127.9 μg/L and the RH from 10 to 85% resulted in decreases in the toluene degradation rate. For ethanol removal using the MTU-PtTiO₂- 350 catalyst, the degradation rate increased more rapidly with an increase in RH from 17 to 56%; the RH had little effect on the ethanol degradation rate while it further increased from 56% to 82%. We discuss applicability of the model to estimate the influence of process variables and to evaluate photocatalyst performance.     

Potential Impact on Standards for Toxic Air Contaminants

Since the Bhopal incident, the public has placed pressure on regulatory agencies to set community exposure limits for the dozens of chemicals that may be released by manufacturing facilities. More or less objective limits can be established for the vast majority of these chemicals through the use of risk assessment. However, each step of the risk assessment process (i.e., hazard identification, dose-response assessment, exposure assessment, and risk characterization) contains a number of pitfalls that scientists need to avoid to ensure that valid limits are established. For example, in the hazard identification step there has been little discrimination among animal carcinogens with respect to mechanism of action or the epidemiology experience. In the dose-response portion, rarely is the range of “plausible” estimated risks presented. Physiologically based pharmacokinetic (PB-PK) models should be used to understand the difference between the tissue doses and the administered dose, as well as the difference in target tissue concentrations of the toxicant between rodents and humans. Biologically-based models like the Moolgavkar-Knudson-Venzon (MKV) should be developed and used, when appropriate. The exposure assessment step can be significantly improved by using more sensitive and specific sampling and analytical methods, more accurate exposure parameters, and computer models that can account for complex environmental factors. Whenever possible, model predictions of exposure and uptake should be validated by biological monitoring of exposed persons (urine, blood, adipose) or by field measurements of plants, soil, fish, air, or water. In each portion of an assessment, the weight of evidence approach should be used to identify the most defensible value. In the risk characterization, the best estimate of the potential risk as well as the highest plausible risk should be presented. Future assessments would be much improved if quantitative uncertainty analyses were conducted. Procedures are currently available for making future assessments. By correcting some of these shortcomings in how health risk assessments have been conducted, scientists and risk managers should be better able to identify scientifically appropriate ambient air standards and emission limits.     

APM-3 Recommended Standard Methods for Continuing Air Monitoring for Gaseous Contaminants

The purpose of Manual APM-3 is to provide a guide which will help increase the uniformity between various surveys, and thereby increase the useability of the data by others.     

Contaminants of food

A scheme has been developed to rank 70 industrial organic chemicals in order of their priority for further study as potential contaminants of food. Numerical scales were developed for the following seven key criteria concerning environmental issues, food and toxicity:

-Production volume

-Pattern of usage

-Possible fate in the environment

-Likelihood of chemical entering the food chain

-Mechanism of entry into the food chain

-Persistence and accumulation in the food chain

-Toxicity.

Each chemical was assigned a score for the above criteria, which were combined to give an overall ranking for the chemicals. This scheme has been endorsed by the MAFF Steering Group on Chemical Aspects of Food Surveillance. It will be used in the assessment of relative priorities for further non-statutory surveillance for these contaminants in the UK food supply.     

Recommended Procedures for Measuring Odorous Contaminants in the Field

Although the perception of odorous contaminants cannot be precisely described, certain basic facts about human olfaction are known. With known facts or principles, it is possible to investigate odorous contaminants for air pollution control purposes. Odor remains, however, a very intangible commodity. Odorous contaminant investigations must be tailored to the individual problem or locality. Consequently, methods herein described were designed for individuals who have a working knowledge of either odor or air pollution problems. Background references are available for workers who are not familiar with either field.^1-8 This method will describe generalized facts concerning odors as well as subjective and objective methods for measuring odorous contaminants in the field. The use of specific portions of the method depends upon each individual investigation.     

催化湿式氧化法稀土系列催化剂的研究进展

催化湿式氧化法在废水处理中,对高浓度难降解有机物及有毒有害物质具有很好的处理效果,并且具有适应范围广、处理效率高、反应速度快、二次污染低等优点,近年来成为国内外研究的热点.而其中研制具有较高活性、普适性、耐久性的高效催化剂仍是该技术研究的热点和工业应用的关键.因此,有必要阐述近年有关催化剂的研究进展及发展方向.     

微生物降解土壤中石油污染物的研究进展

石油的开采、加工、输送及使用过程中，对大气、土壤、水体带来了严重污染，目前在利用微生物降解石油污染物的研究已有很多，并筛选出许多可降解石油污染物的细菌和真菌，这些菌株在降解过程中，主要受营养元素和表面活性的影响，特别是在多环芳烃的微生物降解方面，因此，针对国内外在石油污染物生物降解方面的研究成果进行了综述及展望。     

Contaminants in waste foundry sand and its leachate

The environmental characteristics of Waste Foundry Sands (WFS), including chemicals in WFS and its leachate, are essential in understanding the environmental impact, rational disposal and potential development of beneficial applications of this solid industrial waste. This paper presents an assessment of broad-spectrum chemicals (metallic, non-metallic and organic chemicals) in aspects of their statistics (mean, median and the 95th percentile) in dry-weight WFS and WFS leachates based on laboratory measurements of 594 WFS samples from 123 foundry facilities in the USA. Results indicate that WFS is basically not hazardous except a risk associated with WFS from copper-based foundry facilities. Leachability of metallic chemicals varies among investigated WFS. A clear delineation between different leaching protocols is implicated.     

Analysis of Temporal and Spatial Dichotomous PM Air Samples in the El Paso-Cd. Juarez Air Quality Basin

ABSTRACT

This paper presents and discusses the results obtained from the gravimetric and chemical analyses of the 24-hr average dichotomous samples collected from five sites in the El Paso-Cd. Juarez air quality basin between August 1999 and March 2000. Gravimetric analysis was performed to determine the temporal and spatial variations of PM_2.5 (particulate matter less than 2.5 um in diameter) and PM2.5-10 (particulate matter less than 10 μm but greater than 2.5 μm in diameter) mass concentrations. The results indicate that ~25% of the PM10 (i.e., PM2.5 + PM2.5-10) concentration is composed of PM2.5. Concurrent measurements of hourly PM concentrations and wind speed showed strong diurnal patterns of the regional PM pollution. Results of X-ray fluorescence (XRF) elemental analyses were compared to similar but limited studies performed by the Texas Natural Resource Conservation Commission (TNRCC) in 1990 and 1997. Major elements from geologic sources—Al, Si, Ca, Na, K, Fe, and Ti—accounted for 35% of the total mass concentrations in the PM2.5-10 fraction, indicating that geologic sources in the area are the dominant PM sources. Levels of toxic trace elements, mainly considered as products of anthropogenic activities, have decreased significantly from those observed in 1990 and 1997.     

Statistical Analysis of Trends in Urban Ozone Air Quality

The purpose of this paper is to demonstrate the use of some statistical methods for examining trends in ambient ozone air quality downwind of major urban areas. To this end, daily maximum 1 -hr ozone concentrations measured over New Jersey, metropolitan New York City and Connecticut for the period 1980 to 1989 were assembled and analyzed. This paper discusses the application of the bootstrap method, extreme value statistics and a nonparametric test for evaluating trends in urban ozone air quality. The results indicate that although there is an improvement in ozone air quality downwind of New York City, there has been little change in ozone levels upwind of New York City during this ten-year period.     

An Analysis of Ozone Generation in Irradiated Houston Air

Ambient ozone measurements in the United States and many other countries are traceable to a National Institute of Standards and Technology Standard Reference Photometer (NIST SRP). The NIST SRP serves as the highest level ozone reference standard in the United States, with NIST SRPs located at NIST and at many U.S. Environmental Protection Agency (EPA) laboratories. The International Bureau of Weights and Measures (BIPM) maintains a NIST SRP as the reference standard for international measurement comparability through the International Committee of Weights and Measures (CIPM). In total, there are currently NIST SRPs located in 20 countries for use as an ozone reference standard. A detailed examination of the NIST SRP by the BIPM and NIST has revealed a temperature gradient and optical path-length bias inherent in all NIST SRPs. A temperature gradient along the absorption cells causes incorrect temperature measurements by as much as 2 °C. Additionally, the temperature probe used for temperature measurements was found to inaccurately measure the temperature of the sample gas due to a self-heating effect. Multiple internal reflections within the absorption cells produce an actual path length longer than the measured fixed length used in the calculations for ozone mole fractions. Reflections from optical filters located at the exit of the absorption cells add to this effect. Because all NIST SRPs are essentially identical, the temperature and path-length biases exist on all units by varying amounts dependent upon instrument settings, laboratory conditions, and absorption cell window alignment. This paper will discuss the cause of, and physical modifications for, reducing these measurement biases in NIST SRPs. Results from actual NIST SRP bias upgrades quantifying the effects of these measurement biases on ozone measurements are summarized.

Implications: NIST SRPs are maintained in laboratories around the world underpinning ozone measurement calibration and traceability within and between countries. The work described in this paper quantifies and shows the reduction of instrument biases in NIST SRPs improving their overall agreement. This improved agreement in all NIST SRPs provides a more stable baseline for ozone measurements worldwide.     

Closed-Loop Recovery of Site Remediation Gas Phase Contaminants

A novel gas phase treatment system (contaminant absorption and recovery [CAR]) for removal and subsequent recycling of gas phase VOCs from soil vapor extraction/gas stripping systems has been developed. Gas phase removal efficiencies using a packed column contactor exceed 99 percent The VOC-laden absorption fluid is subsequently vacuum-stripped of the VOCs, allowing potential condensation into liquid solvent concentrates. Partition coefficients for trichloroethylene (TCE) in triethylene glycol (TEG) ranged to ca. 5.0 mole fraction gas/mole fraction liquid, indicating a significant capacity for removal from the gas phase. Results of pilot-scale operation indicate favorable removal efficiencies and cost-effective performance in comparison to GAC or thermal destruction processes. System mass transfer coefficient predictions were done, using a variety of mathematical models and compared to experimental results. A modified Mangers and Ponten correlation was found to describe system mass transfer coefficients well. The impact of water carry-over on TCE/TEG partitioning was found to be significant. The standard change in entholpy (ΔH°) and the standard change in volume (ΔV°) values were also calculated, and predictions of temperature and pressure on system performance were evaluated.     

Contaminants in the coastal karst aquifer system along the Caribbean coast of the Yucatan Peninsula, Mexico

Intensive land development as a result of the rapidly growing tourism industry in the “Riviera Maya” region of the Yucatan Peninsula, Mexico may result in contamination of groundwater resources that eventually discharge into Caribbean coastal ecosystems. We deployed two types of passive sampling devices into groundwater flowing through cave systems below two communities to evaluate concentrations of contaminants and to indicate the possible sources. Pharmaceuticals and personal care products accumulated in the samplers could only have originated from domestic sewage. PAHs indicated contamination by runoff from highways and other impermeable surfaces and chlorophenoxy herbicides accumulated in samplers deployed near a golf course indicated that pesticide applications to turf are a source of contamination. Prevention and mitigation measures are needed to ensure that expanding development does not impact the marine environment and human health, thus damaging the tourism-based economy of the region.     

An Analysis of State Air Pollution Conrol Expenditures

Air pollution control, a significant problem facing state governments, receives a varying amount of fiscal resources in each state. The purpose of this paper is to examine social, economic, and political factors that may be related to state air pollution control expenditures. The indicators of the social-economic factors are urbanization, industrial pollution potential, income, and industrialization. The indicators of the political system are interparty competition, malapportionment, voter participation, local control effort, and general state expenditure efforts. The findings show that the few states expending for air pollution control in 1963 were, for the most part, characterized by a high level of economic development. In 1967, states at all levels of economic development allocated revenues for air pollution, although the more developed continued to hold an edge. In neither year did the political variables differentiate between levels of expenditure. The reasons advanced for the expenditure behavior in 1963 are the historical predominance of local control and the structural limitations of state governments. The wider, and increased, expenditures in 1967 are assessed to be the result of federal grants, the vigorous effort put forth by state control officials, and the increased public concern for the problem.