The microstructure and compression strengths of Ir-15 at. pct X (X ϭ Ti, Ta, Nb, Hf, Zr, or V) binary alloys at temperatures between room temperature and 1800 ЊC were investigated to evaluate the potential of these alloys for ultra-high-temperature use. The fcc and L1 2 two-phase structures of these alloys were examined by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The strengths of the Ir-Ta, -Nb, -Hf, and -Zr alloys were above 800 MPa at temperatures up to 1200 ЊC and about 200 MPa at 1800 ЊC. The strengths of these alloys under 1000 ЊC are equivalent to or higher than those of the commercially used Ni-base superalloys, MAR-M247 and CMSX-10. The Nb concentration dependence of strength was investigated using a series of Ir-Nb alloys with Nb concentrations from 0 to 25 at. pct. It was found that the Ir-base alloys were strengthened by L1 2 precipitation hardening. The potential of the Ir-base alloys for ultra-high temperature use is discussed.

Beyond Ni-Based Superalloys OverviewResearch on platinum-group-metal (PGM)-based intermetallic compounds, which are candidates as hightemperature structural materials, is reviewed in this article. The research reviewed focuses on PGM-based L1 2 and B2 compounds. Alloys with a face-centered cubic and L1 2 or B2 phase are also reviewed.

The surface electronic structure and CO-oxidation activity of Pt and Pt alloys, Pt3T (T = Ti, Hf, Ta, Pt), were investigated. At temperatures below 538 K, the CO-oxidation activities of Pt and Pt3T increased in the order Pt < Pt3Ti < Pt3hHf < Pt3Ta. The center-of-gravity of the Pt d-band (the d-band center) of Pt and Pt3T was theoretically calculated to follow the trend Pt3Ti < Pt3Ta < Pt3Hf < Pt. The CO-oxidation activity showed a volcano-type dependence on the d-band center, where Pt3Ta exhibited a maximum in activity. Theoretical calculations demonstrated that the adsorption energy of CO on the catalyst surface monotonically decreases with the lowering of the d-band center because of diminished hybridization of the surface d-band and the lowest-unoccupied molecular orbital (LUMO) of CO. The observed volcano-type correlation between the d-band center and the CO oxidation activity is rationalized in terms of the CO adsorption energy, which counterbalances the surface coverage by CO and the rate of CO oxidation.

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A platinum-based intermetallic phase with an early d-metal, Pt(3)Ti, has been synthesized in the form of nanoparticles (NPs) dispersed on silica (SiO(2)) supports. The organometallic Pt and Ti precursors, Pt(1,5-cyclooctadiene)Cl(2) and TiCl(4)(tetrahydrofuran)(2), were mixed with SiO(2) and reduced by sodium naphthalide in tetrahydrofuran. Stoichiometric Pt(3)Ti NPs with an average particle size of 2.5 nm were formed on SiO(2) (particle size: 20-200 nm) with an atomically disordered FCC-type structure (Fm3m; a = 0.39 nm). A high dispersivity of Pt(3)Ti NPs was achieved by adding excessive amounts of SiO(2) relative to the Pt precursor. A 50-fold excess of SiO(2) resulted in finely dispersed, SiO(2)-supported Pt(3)Ti NPs that contained 0.5 wt % Pt. The SiO(2)-supported Pt(3)Ti NPs showed a lower onset temperature of catalysis by 75 degrees C toward the oxidation reaction of CO than did SiO(2)-supported pure Pt NPs with the same particle size and Pt fraction, 0.5 wt %. The SiO(2)-supported Pt(3)Ti NPs also showed higher CO conversion than SiO(2)-supported pure Pt NPs even containing a 2-fold higher weight fraction of Pt. The SiO(2)-supported Pt(3)Ti NPs retained their stoichiometric composition after catalytic oxidation of CO at elevated temperatures, 325 degrees C. Pt(3)Ti NPs show promise as a catalytic center of purification catalysts for automobile exhaust due to their high catalytic activity toward CO oxidation with a low content of precious metals.