Journal
SEPARATION AND PURIFICATION TECHNOLOGY
Volume 237, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.seppur.2019.116366
Keywords
Ultrafiltration; Oxyfluorfen; Non-polar organochlorine; BDD; Electrochemical oxidation
Categories
Funding
- European Union [CTM2016-76197-R]
- CONACyT, Mexico [CVU 264785]
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The present work deals with the use of ultrafiltration as a pre-concentration stage in the electrochemical degradation of a non-polar organochlorine compound (oxyfluorfen) with boron-doped diamond (BDD) anodes. The first stage of the work consisted in evaluating the performance of a pilot scale ultrafiltration unit to concentrate a solution of a commercial formulation of oxyfluorfen (Barre (R)) at total recirculation mode. The ultrafiltration membrane exhibited a total rejection of oxyfluorfen, around 70% rejection of TOC and a permeate flux of 285.1 L h(-1) m(-2) at 4 bar and 25 degrees C. The rejection of oxyfluorfen is higher than expected due to the presence of surfactant compounds in the commercial formulation selected, which promotes a mechanism of micellar enhanced ultrafiltration. Next, a discontinuous ultrafiltration test was performed, maintaining this high rejection of oxyfluorfen and observing a limited contribution of fouling mechanisms, according to the adjustment of the data to fouling models. Regarding the electrochemical oxidation of the concentrate with BDD anodes, it was observed an increase in the specific power consumption from 590 kWh kg(-1) for the raw solution to 882 kWh kg(-1) for the concentrate. This unexpected result can be explained due to the limited rejection of the soluble fraction in the ultrafiltration stage, what produced a lower concurrence of oxidants in the electrochemical oxidation step. According to these results, it can be stated that it is worth using ultrafiltration as a concentration stage for commercial formulations of non-polar organochlorines with both high rejection and flux, although it should be combined with degradation technologies different from electrochemical oxidation.
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