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BACKGROUND: One of the most important industrial sources of volatile organic compounds (VOCs) is related to coating and painting applications. In this sense, photocatalytic oxidation can become an innovative and promising alternative for the remediation of air polluted by VOCs. In this study the UV photodegradation of m-xylene, toluene and n-butyl acetate, as representative compounds of paint solvents, was carried out in an annular reactor using a TiO 2 -glass wool supported catalyst.

A 0.75-m 3 pilot-scale biotrickling filter was run for over 1 yr in a Spanish furniture company to evaluate its performance in the removal of volatile organic compounds (VOCs) contained in the emission of two different paint spray booths. The first one was an open front booth used to manually paint furniture, and the second focus was an automatically operated closed booth operated to paint pieces of furniture. In both cases, the VOC emissions were very irregular, with rapid and extreme fluctuations. The pilot plant was operated at an empty bed residence time (EBRT) ranging from 10 to 40 sec, and good removal efficiencies of VOCs were usually obtained. When a buffering activated carbon prefilter was installed, the system performance was improved considerably, so a much better compliance with legal constraints was reached. After different shutdowns in the factory, the period to recover the previous performance of the biotrickling reactor was minimal. A weekend dehydration strategy was developed and implemented to control the pressure drop associated with excessive biomass accumulation.

International audienceThis paper deals with the 3-methylbutanal ((CH3)2CHCH2COH) removal with the help of a nonthermal surface plasma discharge coupled with photocatalysis. The capability of this process for gas treatment was studied. A planar reactor system was developed in order to perform the effect of adding photocatalytic material in plasma surface discharge barrier dielectric (SDBD) zone on (i) 3-methylbutanal removal, (ii) selectivity of CO2 and CO, (iii) byproducts formation such ozone formation. It was found that the influence of the UV light generated by SDBD reactor was very low. The activation of the photocatalyst media could be negligible. Whereas, the introduction of external UV light to the process improves significantly the removal efficiency of 3-methylbutanal (3MBA) and the mineralization. A synergetic effect was observed by combining plasma SDBD and photocatalysis from all experiments and with other pollutant such as trimethylamine (N(CH3)3). Moreover, the byproducts of 3MBA were identified and evaluated with plasma SDBD, photocatalysis and plasma SDBD/photocatalysis combination

The abatement of typical paint solvent compounds as individuals and in mixtures was carried out in an annular TiO 2 supported reactor, for concentrations up to 900 mg C m −3 . Two different fiberglass supports were compared, and the catalyst supported over a fiber mat showed better performance, with a lower pressure drop (>35% of reduction) and a slightly higher removal efficiency (about 2%) than that supported over glass wool. For every target compound in the whole range of relative humidity studied (4−75%), the photocatalytic activity increased with the air water content. The removal of the compounds in the binary and ternary mixtures was depressed, even >90% for toluene, compared with individual tests. Xylene was the main compound responsible for the inhibition effects in the mixtures, followed by toluene and butyl acetate. Photodegradation of individual compound data was well fitted by both simple and bimolecular Langmuir−Hinselwood (LH) kinetic models.