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Biofiltration of a styrene/acetone vapor mixture in two reactor types under conditions of acetone overloading
Author(s) -
Paca Jan,
Halecky Martin,
Novak Vratislav,
Jones Kim,
Kozliak Evguenii
Publication year - 2012
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/jctb.3732
Subject(s) - acetone , styrene , chemistry , biofilter , solvent , biodegradation , polystyrene , solubility , chromatography , waste management , organic chemistry , polymer , engineering , copolymer
Abstract BACKGROUND: Evaluation of the biodegradation interactions between styrene and acetone, two typical paint solvents and vapor phase pollutants differing in water solubility and biodegradability, was conducted both in a trickle bed reactor (TBR) and a biofilter (BF). The loading rate experiments were performed by increasing the acetone concentration in the inlet air while keeping the styrene concentration and loading rate constant. RESULTS: At acetone loading rates (OL AC ) between 25 and 35 g c m −3 h −1 , the BF featured greater steady state performance characteristics for styrene degradation. At OL AC between 35 and 48 g c m −3 h −1 , a decline of removal efficiency (RE) was observed for both pollutants, due to the system's overloading with acetone. Increasing OL AC above 52‐55 g c m −3 h −1 in both reactors resulted in drifts of RE and EC over time to much lower values. A step‐drop of acetone loading rate back to OL AC of 3 g c m −3 h −1 (g c denotes grams of carbon) resulted in lag periods lasting for several hours. CONCLUSIONS: Two important issues inherent for acetone biofiltration, e.g., from paint booths or polystyrene production, were identified: (1) poor performance at high loadings of this aggressive solvent and (2) acetone back‐stripping into the air following periods of high overloading. Copyright © 2012 Society of Chemical Industry