Hydrodehalogenation of chlorobenzene on activated carbon and activated carbon supported catalysts.

Abstract:

:Chlorinated aromatic compounds in (waste) gases can be removed and/or dehalogenated by passing over a bed of activated carbon (AC) in a hydrogen containing atmosphere. Dehalogenation of the model compound chlorobenzene (PhCl) to HCl is complete at 490 degrees C--rather than the approximately 900 degrees C needed for the mere gas-phase reaction--but part of the benzene moieties is retained on the AC, resulting in its rather rapid deactivation, apparently due to a large decrease in surface area. Therefore, <1 mmol PhCl per gram of 'catalyst' could be processed. At 600 degrees C chlorobenzene yields 100% of both HCl and benzene, but still the AC lost most of its activity in time. Performances are compared of three different commercial ACs. As a HCl-washed AC is just as active, metals are not involved. This acid-washed AC was used as a support for 10 wt% Ni or Fe catalysts. While Fe did not show appreciable activity, results with Ni are promising. The yields of HCl and benzene from PhCl are approximately 100% already at T<400 degrees C, and T(50%) congruent with 260 degrees C, over 200 degrees C lower than with AC alone. There is no appreciable decrease of activity after having injected >20 mmol PhCl per gram of catalyst at partial conversion.

journal_name

Chemosphere

journal_title

Chemosphere

authors

Santoro D,de Jong V,Louw R

doi

10.1016/s0045-6535(02)00579-9

subject

Has Abstract

pub_date

2003-03-01 00:00:00

pages

1255-60

issue

9

eissn

0045-6535

issn

1879-1298

pii

S0045-6535(02)00579-9

journal_volume

50

pub_type

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