Platinum sintering

Most reforming catalysts would start platinum sintering at around 480°C in Nj, but any oxygen present may protect the catalysts from sintering during the dehydration step. 

Figure 31 Platinum sintering under different atmospheres. Catalyst 1 0, H2 ...

Figure 34 Platinum sintering under hydrogen. Comparison between Pt/Al203 and Pt-Ge/Al203. T = 923 K H2 = 2000 L h-i kg-. ...

The packaging approach utilized for tliis battery is similar to that for nickel—hydrogen single cylindrical cells as shown in Figure 23. The sdv er electrode is typically the sintered type used in rechargeable sdv er—zinc cells. The hydrogen electrode is a Teflon-bonded platinum black gas difhision electrode. 

A typical converter is made up of multiple furnaces, each of which contains 8 to 10 reactors. Each reactor is made up of 10 to 30 sintered alumina tubes lined with platinum. The furnaces are direct fired with natural gas to 1200—1300°C. A typical furnace can produce about 125 t per month of hydrogen cyanide. Catalyst life is approximately 10,000 h. 

Nonselective catalytic reduction systems are often referred to as three-way conversions. These systems reduce NO, unbumed hydrocarbon, and CO simultaneously. In the presence of the catalyst, the NO are reduced by the CO resulting in N2 and CO2 (37). A mixture of platinum and rhodium has been generally used to promote this reaction (37). It has also been reported that a catalyst using palladium has been used in this appHcation (1). The catalyst operation temperature limits are 350 to 800°C, and 425 to 650°C are the most desirable. Temperatures above 800°C result in catalyst sintering (37). Automotive exhaust control systems are generally NSCR systems, often shortened to NCR. 

CjgHjoOgNa. SHgO, m.p. 304° (dec.), after sintering at 285°, acid to litmus, decolourises permanganate absorbs 2 mols, of hydrogen ir presence of platinum oxide as a catalyst. 

Platinum serves as the catalyst for the oxidation of CO and hydrocarbons. It is relatively insensitive to contamination by lead or sulfur. At high temperatures it is not known to dissolve in the washcoat, but sintering into larger particles may lead to a substantial loss of platinum surface area with dramatic consequences for the overall oxidation activity. 

SEM and EDS analysis of the platinum-doped tungsten oxide photocatalyst after sintering showed the presence of platinum particles on the surface of the tungsten oxide. 

Figure 4 is a back-scattered electron image of the sintered platinum-doped tungsten oxide photocat yst (the bri t spheres are platinum). Analysis of the sintered platinum-doped tungsten oxide by ESCA reveal that the platinum the surface is Pt. ... 

We used polycrystalline films of ZnO and Sn02 as adsorbents. The films were deposited from the water suspension of respective oxides on quartz substrates. These substrates contained initially sintered contacts made of platinum paste. The gap between contacts was of about lO" cm. All samples were initially heated in air during one hour at T 500 C. We used purified molecular oxygen an acceptor particle gas. H and Zn atoms as well as molecules of CO were used as donor particles. We monitored both the kinetics of the change of ohmic electric conductivity and the tangent of inclination angle of pre-relaxation VAC caused by adsorption of above gases and the dependence of stationary values of characteristics in question as functions of concentrations of active particles. 

When a platinum wire (which may have been hot) was dipped for a flame test into a sintered funnel containing the air-dried complex, detonation occurred. This may have been due to heat and/or friction on a compound containing both strongly oxidising and reducing radicals. Avoid dipping (catalytically active) platinum wire into bulk samples of materials of unknown potential. 

X-Ray studies confirm that platinum crystallites exist on carbon supports at least down to a metal content of about 0.03% (2). On the other hand, it has been claimed that nickel crystallites do not exist in nickel/carbon catalysts (50). This requires verification, but it does draw attention to the fact that carbon is not inert toward many metals which can form carbides or intercalation compounds with graphite. In general, it is only with the noble group VIII metals that one can feel reasonably confident that a substantial amount of the metal will be retained on the carbon surface in its elemental form. Judging from Moss s (35) electron micrographs of a reduced 5% platinum charcoal catalyst, the platinum crystallites appear to be at least as finely dispersed on charcoal as on silica or alumina, or possibly more so, but both platinum and palladium (51) supported on carbon appear to be very sensitive to sintering. 

---