This article describes the overall development, including formulation and calibration, of linear and nonlinear multiple regression models for predicting total trihalomethane formation potential and kinetics during the chlorination of natural waters. The rationale behind each model formulation is discussed, and statistics relating to the calibration of each model are presented. The testing and attempted validation of these models are also addressed. Each model is subjected to a sensitivity analysis and a validation analysis using data derived from the literature.

Removal of dissolved organic and inorganic contaminants is an anticipated benefit of the biofiltration of drinking water; however, common biofiltration design and operational practices do not seek to enhance the biological activities associated with those removals. A pilot‐scale study identified two enhancement strategies—nutrient and peroxide dosing—that improved both water quality and hydraulic performance of a biofilter. These strategies control the formation of extracellular polymeric substances (a potential foulant of biological filters) while maintaining or increasing microbial activity. Biofilter nutrient enhancement was found to decrease terminal head loss by ~ 15% relative to a control filter with no nutrient enhancement. Nutrient enhancement also sustainably decreased breakthrough of 2‐methylisoborneol (MIB), manganese (Mn), and dissolved organic carbon (DOC). Peroxide enhancement was performed to increase oxidative action of biofilter microorganisms and promote the oxidation of inactive biomass. Peroxide enhancement decreased terminal head loss up to ~ 60% relative to the control filter, while maintaining MIB, Mn, and DOC treatment performance. This case study is an important step in moving the practice of biofiltration from a passive process to a purposefully operated biological system, i.e., engineered biofiltration.

No abstract

A magnetically agitated photocatalytic reactor (MAPR) has been developed and assessed for oxidation of phenol. The MAPR uses a titanium dioxide composite photocatalyst with a ferromagnetic barium ferrite core. The catalyst motion was controlled with a dual-component magnetic field. First, a permanent magnet above the reactor provided a static magnetic field to counteract the force of gravity, hence increasing catalyst exposure to UV. Second, an alternating magnetic field generated by a solenoid was used to agitate the catalyst, thus increasing mass transfer between pollutants and byproducts to the catalyst. Optimal performance of the MAPR was achieved with the permanent magnet present and 1 A of alternating current to the solenoid between 20 and 80 Hz. Operating with a 60-Hz signal at 1 A with the permanent magnet present and 100 mg of catalyst, the system reduced an 11 mg/L phenol concentration by97% and decreased nonpurgeable dissolved organic carbon by 93% in 7 h using three 8-W 365-nm peak UV lamps.

Haloacetic acids (HAAs) are environmentally and medically important chemicals. No analytical method is currently available to analyze EPA-regulated HAAs in biological samples at environmentally relevant low concentrations. Clinical studies of this class of chemicals are also limited by the lack of analytical techniques of high sensitivity and precision. We now report a new analytical method using gas chromatography/ion trap mass spectrometry for quantifying nine HAAs present inplasma, urine, and water at picogram per milliliter levels. The derivatization reactions of HAAs with pentafluorobenzyl bromide were optimized and detection with an electron capture negative ion chemical ionization mode was employed to enhance the sensitivity. Selected ion monitoring and selected reaction monitoring methods were utilized for quantitation. The detection limits of HAAs in plasma, urine, and water were 25-1000 pg/mL. Accuracies varied from 86.6 to 118.1% (intraday) and 81.7 to 119.6% (interday). Precisions (CV) varied from 0.9 to 19.9% (intraday) and 0.8 to 19.8% (interday), and linearities (r2) varied from 0.9732 to 0.9998 (intraday) and 0.9422 to 0.9987 (interday), respectively. Methyl tertbutyl ether and diethyl ether provided the highest extraction recoveries for the HAAs (74.9-107.2%). The method was applied successfully to a kinetic investigation of low levels of HAAs in humans consuming chlorinated drinking water.