Pd-Cu catalysts supported on anion exchange resin for the simultaneous catalytic reduction of nitrate ions and reductive dehalogenation of organochlorinated pollutants from water
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Titre | Pd-Cu catalysts supported on anion exchange resin for the simultaneous catalytic reduction of nitrate ions and reductive dehalogenation of organochlorinated pollutants from water |
Type de publication | Journal Article |
Year of Publication | 2019 |
Auteurs | Bradu C, Capat C, Papa F, Frunza L, Olaru E-A, Crini G, Morin-Crini N, Euvrard E, Balint I, Zgura I, Munteanu C |
Journal | APPLIED CATALYSIS A-GENERAL |
Volume | 570 |
Pagination | 120-129 |
Date Published | JAN 25 |
Type of Article | Article |
ISSN | 0926-860X |
Mots-clés | Anion exchange resin, Hydrodechlorination, Nitrate reduction, Pd-Cu catalyst, Water treatment |
Résumé | The present work proposes the simultaneous removal of these classes of pollutants by a catalytic hydrotreatment processes. For this purpose, bimetallic Pd-Cu catalysts (with mass ratio Pd:Cu of 4:1) supported on macroporous strong base anion resin were prepared by different methods. The catalysts were characterized (by XRD, SEMEDX, XPS, AAS and H-2 chemisorption) and tested in a continuous flow system. The selected catalyst preparation protocol consists in a two-step method, which implies the deposition of palladium by ion exchange and the subsequent deposition of copper by controlled reaction on the surface of the pre-reduced palladium. The effectiveness of the catalyst in the simultaneous reduction of nitrate and hydrodechlorination of 4-chlorophenol was demonstrated. By adjusting the initial pH and the flow rate of the aqueous solution, nearly complete hydrodechlorination of 4-chlorophenol can occur together with selective nitrate reduction at a conversion of 95% and a selectivity to N-2 of 92% (this value contains the contribution of all gaseous products, including the eventually formed NOx). The bimetallic catalyst was found to remains relatively stable after 100 h of test time. |
DOI | 10.1016/j.apcata.2018.11.002 |