Nanocrystalline ZrO(2) and Pt-doped ZrO(2) catalysts for low-temperature CO oxidation

Zirconia (ZrO(2)) nanoparticles were synthesized by solution combustion using urea as an organic fuel. Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), transmission electron microscopy (TEM), UV–vis and Fourier transform infrared (FTIR) measurements were performed in order to characterize the catalyst. The calculated crystallite size of ZrO(2,) calculated with the help of the Scherrer equation, was around 30.3 nm. The synthesized ZrO(2) was scrutinized regarding its role as catalyst in the oxidation of carbon monoxide (CO). It showed 100% CO conversion at 240 °C, which is the highest conversion rate reported for ZrO(2) in literature to date. It is found that through solution combustion, Pt(2+) ions replace Zr(4+) ions in the ZrO(2) lattice and because of this, oxygen vacancies are formed due to charge imbalance and lattice distortion in ZrO(2). 1% Pt was doped into ZrO(2) and yielded excellent CO oxidation. The working temperature was lowered by 150 °C in comparison to pure ZrO(2). Further, it is highly stable for the CO reaction (time-on-stream ≈ 40 h). This is because of a synergic effect between Pt and Zr components, which results in an increase of the oxygen mobility and oxygen vacancies and improves the activity and stability of the catalyst. The effects of gas hourly space velocity (GHSV) and initial CO concentration on the CO oxidation over Pt(1%)-ZrO(2) were studied.