Activity of metal phosphate catalyst in selective reduction of NO with C3H6
was investigated. It was found that Co-3(PO4)(2) and GaPO4 exhibited high
catalytic activities in NO selective reduction with C3H6 Among the metal ph
osphates tested, Co-3(PO4)(2) exhibited the highest activity. In addition,
thermal stability of this catalyst is sufficient to meet practical applicat
ion. Co-3(PO4)(2) catalyst, therefore, is promising as a thermostable de-NO
, catalyst for lean combustion engines. Selective reduction of NO hardly pr
oceeded when CH4 was used as reductant. It was found, however, that loading
Pt on Co-3(PO4)(2) is effective for improving the activity in selective re
duction of NO. The reaction mechanism in reduction of NO over Co-3(PO4)(2)
catalyst was further studied with temperature programmed desorption (TPD) t
echniques. Results of NO-TPD and NO direct decomposition experiments sugges
ted that N-2 was formed by the dissociative adsorption of NO which is the i
nitial reaction step in NO reduction. On the other hand, adsorption of oxyg
en on this catalyst is too strong to desorb. Therefore, it is considered th
at propene as a reductant removes the surface oxygen formed by decompositio
n of NO. In conclusion, this study revealed that Co-3(PO4)(2) is highly act
ive and selective in reduction of NO with hydrocarbon, in the presence of o
xygen.