Relationship between chlorine consumption and chlorination by-products formation for model compounds

The objective of this research is to investigate the relationship between chlorine decay and the formations of disinfection by-products (DBP), including trichloromethane (TCM) and chloroacetic acid (CAA) in the presence of four model compounds, i.e., resorcinol, phloroglucinol, p-hydroxybenzoic acid, and m-hydroxybenzoic acid. The chlorine degradation in model compounds with OH and/or COOH functional groups were rapid after chlorination. The TCM yields of carboxylic group substituted compounds (3-hydroxybenzoic acid [3-HBA], 4-hydroxybenzoic acid [4-HBA]) were found to be lower than that of the m-dihydroxy substituted compounds. Phloroglucinol, with one more OH substitution group than resorcinol, tends to form significant amounts of CAA after chlorination. However, it was observed that with the COOH substitution of 3-HBA and 4-HBA tend to exhibit more CAA formation potential than resorcinol. The developed parallel second and first-order reaction model for chlorine demand has been successfully utilized for TCM, CAA and DBP formation modeling. A high correlation between CAA and TCM was observed for the model compounds.     

Degradation of carbofuran in water by solar photocatalysis in presence of photosensitizers

The effect of the presence of photosensitizers, methylene blue (MB) and rose Bengal (RB), on the degradation of carbofuran (2,3-dihydro-2,2-dimethylbenzofuran-7-yl methylcarbamate) in water in a solar photocatalytic system was investigated. It was found that as compared to MB, RB generally showed a stronger effect on the decomposition of carbofuran under comparable conditions. Among the conditions studied, adding 2 x 10(-6) M of RB, that corresponding to 2% of the initial concentration of carbofuran solution in the system, rendered the most effective degradation of carbofuran. As a result, a carbofuran removal percentage of 69.9%, a mineralization efficiency of 28.0%, and a microtoxicity reduction of 65.0% could be achieved. The degradation and mineralization of carbofuran was found to follow the pseudo-first order reaction kinetics. The decomposition mechanism of carbofuran was further investigated through identification of the intermediates to elaborate the influence of dye photosensitizer on the solar photocatalysis of carbofuran in water. On the basis of the intermediates identified, including carbofuran phenol, 3-hydroxy carbofuran phenol, and substituted alcohols (3-phenoxy 1-propanol, 2-ethyl 1-hexanol, 2-butoxyl ethanol), it appears that hydrolysis and hydroxylation were the two key mechanisms for decomposing carbofuran during the process of solar photocatalysis with the aid of dye photosensitizer.     

A CRAZY IDEA ON URBAN WATER MANAGEMENT?1

ABSTRACT. High percentage of imperviousness in the city is the source of storm runoff. Roof area contributes significantly to the imperviousness. An attempt to make use of roofs as urban flood control device and water conservation measure is advocated. Two different schemes, one for built-up industrial-commercial area, the other for residential area, are suggested. The former utilizes the roof as detention reservoir for flood control, the latter employs recharge pit to convert runoff into ground water resource. The proposed schemes are not only hydrologically, hydraulically and structurally sound but also economically feasible. It is worth considering in the future planning of urban renewal and urban development.     

Remediation of a nonachloro biphenyl congener with zero-valent iron in subcritical water

Dechlorination of a nonachloro biphenyl congener with zero-valent iron in water under high temperature and pressure was investigated over time. Temperature has the main influence on the speed of dechlorination. Determination of polychlorinated biphenyls (PCBs) according to the grade of chlorination was performed by gas chromatography with mass selective detection in single ion monitoring mode. Dechlorination results in a variety of lower chlorinated biphenyls. The level of chlorination decreases with time. The amount of PCB molecules decreases to one-third within 90 min at 250 degrees C and 100 atm. However, no increase of biphenyl could be detected over time. A first-order kinetic model fitted the data obtained.     

The life table and competing risks

The concept of the life table originated in longevity studies of man, where it was always presented as a subject peculiar to public health, demography, and actuarial science. As a result, its development has not received sufficient attention in the field of statistics. Actually, the problems of mortality studies are similar to those of reliability theory and life testing, and they may be described in terms familiar to the statistically oriented mind. From a statistical point of view, human life is a random experiment and its outcome, survival or death, ss subject to chance. The life table systematically records the outcomes of many such experiments for a large number of individuals over a period of time. Thus, the quantities in the table are random variables subject to established statistical analysis. The purpose of this presentation is to discuss the life table from a statistical viewpoint.     

SELECTED NUTRIENTS AND HEAVY METALS IN SEWAGE SLUDGE FROM NEW JERSEY POTWs1

ABSTRACT: In order to determine appropriate application rates and to ensure low pollutant levels in sewage sludge, knowing the chemical composition of sewage sludge is of great importance in a land application program. The objective of this study is to evaluate the variability of selected chemical characteristics of sewage sludge from New Jersey publicly owned treatment works (POTWs). Measurements of total Kjeldahl nitrogen (TKN), NH₄⁺‐N, P, K⁺, Cd, Cu, Pb, and Zn reported by 98 facilities in the 1996 and 1997 New Jersey Sludge Quality Assurance Regulations (SQAR) reports were statistically analyzed. Sewage sludge from Category 5 POTWs (greater than 10 percent industrial input) showed higher Cd, Cu, and Pb concentrations than Category 3 and Category 4 facilities (less than 10 percent industrial input). Even though only two years of data were analyzed, there was an indication that Cd and Pb concentrations in sewage sludge are decreasing with time. The yearly mean of only a few facilities exceeded the federal pollution concentration limits (40 CFR Part 503, Table 3). Phosphorus and Cd values showed the highest variability within facilities based on the coefficient of variation. Due to the variability of sewage sludge constituents, the use of the yearly rolling mean of nutrient concentrations to determine application rates was considered inadequate. An actual analysis of the sewage sludge to be applied is more appropriate to determine application rates than historical data.     

Supercritical fluid extraction of polycyclic aromatic hydrocarbons from white pine (Pinus strobus) needles and its implications

A supercritical fluid extraction (SFE) method was developed for the extraction of polycyclic aromatic hydrocarbons (PAHs) from fresh and fallen pine needles. Toluene-modified CO2 was used as the extracting fluid, and the extracted PAHs were analyzed by GC-MS. Using a two-stage extraction procedure, a static extraction at 180 degrees C and a dynamic extraction at 60 degrees C, and an in-cell silica gel plug plus a post-oven silica gel column, the extraction and fractionation of PAHs can be accomplished in one step. Over a seven month period, a significant variation was observed for PAHs in urban samples, while PAHs in mountain samples were at much lower levels (by a factor of approximately 8) and showed little seasonal change. Although dry fallen needles and fresh needles contained similar amounts of PAHs, in the fallen needles the lower molecular weight PAHs were partially lost while the higher molecular weight PAHs were slightly enriched. Pollution in urban areas was found to be highly localized, and buildings and trees are believed to be important factors in the restriction of atmospheric PAHs.     

Paper fibers as a carbon source for the de novo formation of polychlorinated dioxins and furans

The formation of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDDs/Fs) from carbon that was produced by the pyrolysis of paper fibers and from wood charcoal was investigated experimentally. Fibers obtained from filter paper were pyrolyzed at 300° and 800°C to produce low- and high-temperature carbon samples. The two types of carbon and wood charcoal were mixed with silica (SiO₂) and trace copper oxide to produce three synthetic fly ash samples. Experiments to measure the formation of PCCDs/Fs from the three ash samples were conducted using a bench-scale reactor. The two carbon samples derived from paper fibers generated more PCDDs/Fs than was generated by the wood charcoal. The PCDDs/Fs generated by the low-temperature carbon and by the wood charcoal were dominated by the lower-chlorinated PCDFs. Such unique homologue distribution patterns are very similar to those generated by the open burning of household waste. The high-temperature carbon generated more highly chlorinated PCDDs/Fs. The effect of pyrolysis temperature on the de novo formation of PCDDs/Fs from residual carbon is discussed. Paper and paper products contained in household waste are likely to be the source of unburned carbon that contributes to high PCDD/F emissions in the open burning of household waste.