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Joel Ducoste

Publications and source records attributed to Joel Ducoste.

3 recordsLinked to original sources

Experimental measurements of fluence distribution in a UV reactor using fluorescent microspheres.

One concern with current techniques of UV reactor validation is that they provide only a measure of the mean UV fluence. In this research, the actual fluence distribution of a UV reactor is measured through the use of photochemically active fluorescent microspheres. Experimental tests were performed in a pilot-scale monochromatic UV 254 nm reactor operated at two flow rates. Analysis of the fluorescence intensity decay was performed using collimated beam experiments for determination of decay rate kinetics. A stochastic hierarchal process involving Bayesian statistics, and the Markov chain Monte Carlo integration technique was used to correlate the microsphere fluorescence intensity distribution to the UV fluence distribution. The experimental UV fluence distribution was compared with the fluence distribution predicted using a computational fluid dynamics model. The results showed that the fluorescent microspheres measured a wider distribution of UV fluences with a flow rate of 3 gpm than with 7.5 gpm. The principal differences between the modeled and the measured distribution were in the low UV fluences where the microspheres predicted lower fluence levels than the model. The use of microspheres is demonstrated as a novel technique for measurement of the fluence distribution in UV reactors. This technique has both fundamental and practical implications for reactor evaluation and testing and could improve confidence in the future use of mathematical models for UV reactor characterization. It also serves as a complement to biodosimetry testing by providing greater insights regarding reactor behavior and validation.

Bacillus subtilis↗

Impact of lamp shadowing and reflection on the fluence rate distribution in a multiple low-pressure UV lamp array.

Use of mathematical modeling for determination of ultraviolet (UV) fluence in disinfection reactors requires accurate knowledge of the fluence rate distribution in a multiple lamp array. A method for measuring the fluence rate among a multiple lamp array was demonstrated using spherical actinometry. A matrix of four low-pressure UV lamps in air were investigated to evaluate the potential for shadowing and reflection to impact the fluence rate within and surrounding the lamp array. Two fluence rate distribution models were tested to determine the ability to predict the fluence rate distribution measured by the actinometers. Shadowing proved to attenuate UV light. Reflection from the lamp surface added 3-9% to the fluence rate, depending upon position in the reactor. These effects, as well as the fluence rate at various points in the lamp matrix were effectively modeled using RAD-LSI and UVCalc3D fluence rate distribution models. At fluence rates above 8mWcm(-2), the actinometry measured fluence rate was lower than the modeled rate, presumably from saturation of the actinometer solution at high fluence rates (close to the lamp). With multiple lamp reactors, the impact of shadowing can significantly affect fluence rate distribution and thus the level of microbial inactivation. If shadowing is not included in fluence rate distribution models, the fluence rate will be over predicted in the shadow zone of a neighboring lamp, falsely skewing model inactivation predictions.

Disinfection↗

A non-biological surrogate for sequential disinfection processes.

An evaluation of Fluorescent YG-microspheres (Polysciences Inc.) was performed to simulate Cryptosporidium parvum (C. parvum) oocysts inactivation in treatment systems that utilize multiple disinfectants. Experiments were conducted in batch reactors that included an ozone primary stage and a secondary free chlorine treatment stage. A flow cytometer was used to track changes in the fluorescence intensity distribution due to exposure to the chemical disinfectant. Microsphere 'survival ratios' (N/No) were calibrated by selecting an appropriate fluorescence intensity threshold to replicate the inactivation of different C. parvum oocysts strains. Results showed that fluorescent microspheres displayed synergistic effects in the presence of two sequential disinfectants. In addition, microsphere structural tests showed that the polystyrene surface was damaged due to exposure to ozone. This polystyrene damage enhanced the diffusion of the secondary disinfectant into the microsphere, where dye was degraded in the opened polymer layer. As a result, YG-fluorescent microspheres is a promising non-biological technique that is capable of producing similar synergistic behavior as with C. parvum oocysts exposed to ozone followed by chlorine.

Animals↗