CATALYTIC WET OXIDATION OF P-COUMARIC ACID - PARTIAL OXIDATION INTERMEDIATES, REACTION PATHWAYS AND CATALYST LEACHING

Citation
D. Mantzavinos et al., CATALYTIC WET OXIDATION OF P-COUMARIC ACID - PARTIAL OXIDATION INTERMEDIATES, REACTION PATHWAYS AND CATALYST LEACHING, Applied catalysis. B, Environmental, 7(3-4), 1996, pp. 379-396
Citations number
16
Categorie Soggetti
Chemistry Physical","Engineering, Environmental
ISSN journal
09263373
Volume
7
Issue
3-4
Year of publication
1996
Pages
379 - 396
Database
ISI
SICI code
0926-3373(1996)7:3-4<379:CWOOPA>2.0.ZU;2-3
Abstract
The catalytic oxidation of p-coumaric acid, a compound representative of the polyphenolic fraction typically found in olive processing and w ine-distillery wastewaters, has been investigated using various homoge neous and heterogeneous catalysts. Experiments have been performed wit h homogeneous Fe2+, Cu2+, Zn2+ and Co2+ ions at pH = 1, and with metal oxide catalysts in suspension at pH 3.5, 7 and 12. Additional uncatal yzed experiments have been performed and the results are compared to t hose of the catalyzed runs. The temperature was 403 K and the oxygen p artial pressure was 2.8 MPa in all runs. The distribution of the react ion intermediates was determined, using HPLC and GCMS as the main anal ytical techniques, and reaction pathways are speculated. It was found that the use of catalysts could increase the rate of destruction of p- coumaric acid compared to the uncatalyzed reaction, while the distribu tion of the intermediate compounds was strongly dependent on the pH of the solution. A CuO . ZnO-Al2O3 heterogeneous catalyst was found to b e effective for the oxidation of p-coumaric acid although leaching of dissolved metals to the solution was found to occur. The stability of the heterogeneous catalysts was investigated by measuring the extent o f metal leaching into the solution. The results are discussed with res pect to the impact of various conditions (catalyst, pH) on the oxidati on of p-coumaric acid and compared to those of the uncatalyzed reactio n, studied in previous work.