High activity and regenerability of a palladium-gold catalyst for chloroform degradation

BACKGROUND Chloroform (CF), a common groundwater contaminant, can be degraded in deionized water reductively using Pd and Pd‐Au catalysts under mild conditions (room temperature, atmospheric pressure) via hydrodechlorination (HDC). However, the performance of these catalysts under field‐like conditi...

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Published inJournal of chemical technology and biotechnology (1986) Vol. 91; no. 10; pp. 2590 - 2596
Main Authors Velázquez, Juan C, Leekumjorn, Sukit, Hopkins, Gary D, Heck, Kimberly N, McPherson, Jason S, Wilkens, John A, Nave, Bradley S, Reinhard, Martin, Wong, Michael S
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.10.2016
Wiley Subscription Services, Inc
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Summary:BACKGROUND Chloroform (CF), a common groundwater contaminant, can be degraded in deionized water reductively using Pd and Pd‐Au catalysts under mild conditions (room temperature, atmospheric pressure) via hydrodechlorination (HDC). However, the performance of these catalysts under field‐like conditions is unknown. This study evaluates the lab‐scale performance and optimal operating conditions for flow reactors using Pd/Al2O3 and Pd‐Au/Al2O3. RESULTS Both catalysts were active for CF HDC when tested using deionized water and groundwater spiked with CF. The Pd‐Au catalyst was ∼263× more active than the Pd catalyst using unbuffered deionized water (1550 mL‐gPd−1‐min−1 vs 5.89 mL‐gPd−1‐min−1), and was ∼137× more active using buffered groundwater (1030 mL‐gPd−1‐min−1 vs 7.53 mL‐gPd−1‐min−1). The buffer was a carbonate/citrate mixture optimized to prevent pH drop and scale formation from minerals present in groundwater. A catalytic flow process was designed using a buffer co‐feed and daily regeneration of the catalyst bed. Pd‐Au/Al2O3‐ and Pd/Al2O3‐containing reactors exhibited CF conversions of 65% and 32.5% over 18 days operating at a weight hourly space velocity of 30 h−1. CONCLUSIONS This study provides insights into strategies for long‐term operation of catalytic flow reactors to treat CF in groundwater, and shows the higher CF HDC catalytic efficiency of Pd‐Au over Pd. © 2015 Society of Chemical Industry
Bibliography:World Gold Council
National Science Foundation - No. CBET-1134535
Alliance for Graduate Education and Professoriate - No. AGEP
istex:77211EE791A722B847DC0985E10D6CE379DE2980
ArticleID:JCTB4851
ark:/67375/WNG-T1J2VJD0-R
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0268-2575
1097-4660
DOI:10.1002/jctb.4851