Direct production of hydrogen peroxide with palladium supported on phosphate viologen phosphonate catalysts

Citation
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
Citations number
22
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
JOURNAL OF CATALYSIS
ISSN journal
00219517 → ACNP
Volume
196
Issue
2
Year of publication
2000
Pages
366 - 374
Database
ISI
SICI code
0021-9517(200012)196:2<366:DPOHPW>2.0.ZU;2-Q
Abstract
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.