Vv. Krishnan et al., Direct production of hydrogen peroxide with palladium supported on phosphate viologen phosphonate catalysts, J CATALYSIS, 196(2), 2000, pp. 366-374
The optimization of porous hafnium phosphate viologen phosphonate (HfPOPV(X
)) catalyst, [(HfF)(2)(PO4)(P3PCH2CH2-4,4'-bipyridinium-CH2CH2PO3)]F . 2H(2
)O with Pd-metal nanoaggregates, has been attempted. In addition to the dev
elopment of a novel technique for making this catalyst by hydrothermal inco
rporation, an extensive optimization of the process conditions to make hydr
ogen peroxide from H-2 and O-2 has been carried out. The optimal reaction m
edium for this process was methanol in conjunction with sulfuric acid. Unde
r atmospheric conditions, over 3.5 M H2O2 has been produced in 50 h. A tech
nique has also been developed to measure the water formed from the undesira
ble H2O2 reduction step that occurs in series-parallel. to the desired H2O2
production step. The selectivity toward the production of H2O2 in the case
of the hydrothermally incorporated catalysts is over 70% under atmospheric
conditions. The maximum rate of production of H2O2, achieved in anhydrous
methanol-H2SO4 media and hydrothermally incorporated Pd-HfPOPV(X) is about
4.1 mmol/(g min). However, the rate measured here is probably that of exter
nal mass transfer (at the liquid-gas interface) because the resistance due
to it is the rate-determining step. (C) 2000 Academic Press.