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Palladium platinum

Alkenes react with hydrogen in the presence of a platinum palladium rhodium or nickel catalyst to form the corresponding alkane... [Pg.272]

The conditions for hydrogenation of alkynes are similar to those employed for alkenes In the presence of finely divided platinum palladium nickel or rhodium two molar equivalents of hydrogen add to the triple bond of an alkyne to yield an alkane... [Pg.374]

The most obvious way to reduce an aldehyde or a ketone to an alcohol is by hydro genation of the carbon-oxygen double bond Like the hydrogenation of alkenes the reac tion IS exothermic but exceedingly slow m the absence of a catalyst Finely divided metals such as platinum palladium nickel and ruthenium are effective catalysts for the hydrogenation of aldehydes and ketones Aldehydes yield primary alcohols... [Pg.627]

Nitro groups are readily reduced to primary amines by a variety of methods Cat alytic hydrogenation over platinum palladium or nickel is often used as is reduction by iron or tin m hydrochloric acid The ease with which nitro groups are reduced is especially useful m the preparation of arylamines where the sequence ArH ArN02 ArNH2 IS the standard route to these compounds... [Pg.932]

Hydrogenation over a metal catalyst such as platinum palladium or nickel... [Pg.1211]

Dentistry. Most casting alloys meet the composition and properties criteria of specification no. 5 of the American Dental Association (37) which prescribes four types of alloy systems constituted of gold—silver—copper with addition of platinum, palladium, and 2inc. Composition ranges are specified, as are mechanical properties and minimum fusion temperatures. Wrought alloys for plates also may include the same constituents. Similarly, specification no. 7 prescribes nickel and two types of alloys for dental wires with the same alloy constituents (see Dental materials). [Pg.380]

Table 8 shows the supply to the Western world of platinum, palladium, and rhodium. For each metal. supply kicreased significantly ki the latter... [Pg.165]

The most significant PGM deposit in the United States is at Stillwater, Montana, where PGMs are mined as the primary product. The grade has been estimated as between 13 and 22 g/1, having a platinum—palladium ratio of 1 3.5. The first ore was extracted from Stillwater in 1987 and full production of 1000 t/d was reached in 1990. [Pg.166]

Selenium occurs in the slimes as intermetallic compounds such as copper silver selenide [12040-91 -4], CuAgSe disilver selenide [1302-09-6], Ag2Se and Cu2 Se [20405-64-5], where x < 1. The primary purpose of slimes treatment is the recovery of the precious metals gold, silver, platinum, palladium, and rhodium. The recovery of selenium is a secondary concern. Because of the complexity and variabiUty of slimes composition throughout the world, a number of processes have been developed to recover both the precious metals and selenium. More recently, the emphasis has switched to the development of processes which result in early recovery of the higher value precious metals. Selenium and tellurium are released in the later stages. Processes in use at the primary copper refineries are described in detail elsewhere (25—44). [Pg.327]

By-Product Recovery. The anode slime contains gold, silver, platinum, palladium, selenium, and teUurium. The sulfur, selenium, and teUurium in the slimes combine with copper and sUver to give precipitates (30). Some arsenic, antimony, and bismuth can also enter the slime, depending on the concentrations in the electrolyte. Other elements that may precipitate in the electrolytic ceUs are lead and tin, which form lead sulfate and Sn(0H)2S04. [Pg.203]

Gold Casting and Wrought Alloys. Gold alloys useful ki dentistry may contaki gold, silver, platinum, palladium, iridium, kidium, copper, nickel, tin, kon, and zkic. Other metals occasionally are found ki minor amounts. The effect of each of the constituents is empirical, but some observations have been made. [Pg.482]

Gold, platinum, palladium, and silver are the principal components of most of the solders used for joining both noble and base metal alloys. Some solders for base metal alloys also contain nickel, chromium, and/or cobalt as primary ingredients. [Pg.487]

Silver-containing catalysts are used exclusively in all commercial ethylene oxide units, although the catalyst composition may vary considerably (129). Nonsdver-based catalysts such as platinum, palladium, chromium, nickel, cobalt, copper ketenide, gold, thorium, and antimony have been investigated, but are only of academic interest (98,130—135). Catalysts using any of the above metals either have very poor selectivities for ethylene oxide production at the conversion levels required for commercial operation, or combust ethylene completely at useful operating temperatures. [Pg.458]

Metals and alloys, the principal industrial metalhc catalysts, are found in periodic group TII, which are transition elements with almost-completed 3d, 4d, and 5d electronic orbits. According to theory, electrons from adsorbed molecules can fill the vacancies in the incomplete shells and thus make a chemical bond. What happens subsequently depends on the operating conditions. Platinum, palladium, and nickel form both hydrides and oxides they are effective in hydrogenation (vegetable oils) and oxidation (ammonia or sulfur dioxide). Alloys do not always have catalytic properties intermediate between those of the component metals, since the surface condition may be different from the bulk and catalysis is a function of the surface condition. Addition of some rhenium to Pt/AlgO permits the use of lower temperatures and slows the deactivation rate. The mechanism of catalysis by alloys is still controversial in many instances. [Pg.2094]

Starting with a ceramic and depositing an aluminum oxide coating. The aluminum oxide makes the ceramic, which is fairly smooth, have a number of bumps. On those bumps a noble metal catalyst, such as platinum, palladium, or rubidium, is deposited. The active site, wherever the noble metal is deposited, is where the conversion will actually take place. An alternate to the ceramic substrate is a metallic substrate. In this process, the aluminum oxide is deposited on the metallic substrate to give the wavy contour. The precious metal is then deposited onto the aluminum oxide. Both forms of catalyst are called monoliths. [Pg.480]

Another useful teehnique in kinetie studies is the measurement of the total pressure in an isothermal eonstant volume system. This method is employed to follow the eourse of homogeneous gas phase reaetions that involve a ehange in tlie total number of gaseous moleeules present in the reaetion system. An example is the hydrogenation of an alkene over a eatalyst (e.g., platinum, palladium, or niekel eatalyst) to yield an alkane ... [Pg.159]

Platinum, palladium, and rhodium will function well under milder conditions and are especially useful when other reducible functions are present. Freifelder (23) considers rhodium-ammonia the system of choice when reducing -amino nitriles and certain )5-cyano ethers, compounds that undergo extensive hydrogenolysis under conditions necessary for base-metal catalysis. [Pg.97]

Probably the most significant control technology breakthrough came m 1977, when Volvo released a computer-controlled, fuel-mjected vehicle equipped with a three-way catalyst. The new catalytic converters employed platinum, palladium, and rhodium to simultaneously reduce NO and oxidize CO and HC emissions under carefully controlled oxygen conditions. The new Bosch fuel injection system on the vehicle provided the precise air/fuel control necessary for the new catalyst to perform effectively. The combined fuel control and three-way catalyst system served as the foundation for emissions control on the next generation of vehicles. [Pg.451]

Direct hydroxylation of benzene to phenol could be achieved using zeolite catalysts containing rhodium, platinum, palladium, or irridium. The oxidizing agent is nitrous oxide, which is unavoidable a byproduct from the oxidation of KA oil (see KA oil, this chapter) to adipic acid using nitric acid as the oxidant. [Pg.273]

Platinum, palladium and the normal alloys of platinum used in industry are easily workable by the normal techniques of spinning, drawing, rolling, etc. To present a chemically clean surface of platinum and its alloys after fabrication, they may be pickled in hot concentrated hydrochloric acid to remove traces of iron and other contaminants —this is important for certain catalytic and high-temperature applications. In rolling or drawing thin sections of platinum, care must be taken to ensure that no dirt or other particles are worked into the metal, as these may later be chemically or elec-trolytically removed, leaving defects in the platinum. [Pg.942]

The most widely used methods for the application of coatings of gold, silver and the platinum group metals (platinum, palladium, rhodium, iridium, ruthenium, osmium) to base metals are mechanical cladding and electroplating. [Pg.557]

For the noble metals used in oxidation, the loading is about 0.1 oz per car, with calls for a million ounces per year. The current world production rates of platinum, palladium, and rhodium are 1.9, 1.6, and 0.076 million ounces respectively the current U,S. demand for platinum, palladium, rhodium, and ruthenium are 0.52, 0.72, 0.045, and 0.017 million ounces respectively (72, 73). The supply problem would double if NO reduction requires an equal amount of noble metal. Pollution conscious Japan has adopted a set of automobile emission rules that are the same as the U.S., and Western Europe may follow this creates a demand for new car catalysts approaching the U.S. total. The bulk of world production and potential new mines are in the Soviet Union and South Africa. The importation of these metals, assuming the current price of platinum at 155/oz and palladium at 78/oz, would pose a balance of payment problem. The recovery of platinum contained in spent catalysts delivered to the door of precious metal refiners should be above 95% the value of platinum in spent catalysts is greater than the value of lead in old batteries, and should provide a sufficient incentive for scavengers. [Pg.81]

Hydrogenation catalysts,such as platinum, palladium, nickel, and so on. In this case the reaction is the reverse of double-bond hydrogenation (15-11 and 15-15), and presumably the mechanism is also the reverse, though not much is known. Cyclohexene has been detected as an intermediate in the... [Pg.1510]

Moreau-Colin ML (1972) Electronic Spectra and Structural Properties of Complex Tetracyanides of Platinum, Palladium and Nickel. 10 167-190 Morf WE, see Simon W (1973) 16 113-160... [Pg.251]

The active catalyst platinum, palladium and smaller amounts of rhodium. The total weight of these metals used per converter is less than 2 g. [Pg.107]


See other pages where Palladium platinum is mentioned: [Pg.771]    [Pg.484]    [Pg.43]    [Pg.43]    [Pg.172]    [Pg.176]    [Pg.156]    [Pg.200]    [Pg.220]    [Pg.41]    [Pg.383]    [Pg.49]    [Pg.383]    [Pg.48]    [Pg.942]    [Pg.558]    [Pg.96]    [Pg.571]    [Pg.171]    [Pg.248]    [Pg.76]   


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1,5-Cyclooctadiene, iridium complex palladium and platinum complexes

Allyl Complexes of Palladium and Platinum

Bivalent Nickel, Platinum, and Palladium

Bond Lengths in Palladium and Platinum Analogues

By Palladium and Platinum Catalysts

Catalysis Induced by Platinum and Palladium Nanoparticles

Catalyst platinum/palladium partial oxidation

Colloidal Platinum and Palladium Catalysts by Paal

Complexes of Platinum and Palladium

Compounds of Nickel, Palladium and Platinum

Contain Nickel, Palladium and Platinum

Containing Nickel, Palladium, and Platinum Chains

Gold-Palladium or Platinum

Group 10 (Nickel, Palladium and Platinum)

Group 10 (VIII palladium and platinum

Group 10 Palladium Platinum

Group 10 palladium and platinum

Group VIII Nickel, Palladium and Platinum

Group VIIIC Nickel, Palladium, and Platinum

Hydrogenation palladium/platinum catalyst

Nickel palladium-platinum triad

Nickel, Palladium and Platinum

Nickel, Palladium, and Platinum Complexes Derived from OFCOT

Nickel, Platinum, and Palladium Complexes

Organometallic Compounds of Palladium and Platinum

Organometallic Reactions Involving Hydro-Nickel, -Palladium, and -Platinum Complexes

Osmium-platinum cluster Palladium complex

Palladium and Platinum Catalysts

Palladium and platinum

Palladium and platinum valence

Palladium platinum-carbon

Palladium, Platinum, Silver, and Gold

Palladium, Platinum, Silver, and Gold Porphyrins

Phosphine complexes of platinum and palladium

Phosphine palladium and platinum complexes

Phosphine, bis phenyl-, palladium complex platinum complexes

Phosphine, bis[2 ethyljphenyl-, palladium complex platinum complexes

Platinum and Palladium Black Catalysts by Willstatter

Platinum and Palladium Drugs for Cancer Treatments

Platinum family metals palladium

Platinum group elements palladium

Platinum or Palladium

Platinum palladium compounds

Platinum palladium mixture, thermally

Platinum-palladium catalysts

Platinum-palladium hydrogenolysis

Platinum-palladium poly

Platinum-palladium, isocyanides

Platinum— and Palladium—Amine Complexes

Quadruply Bridged Dinuclear Complexes of Platinum, Palladium

Quadruply Bridged Dinuclear Complexes of Platinum, Palladium, and Nickel

Recent Advances in the Stereochemistry of Nickel, Palladium, and Platinum

Separating Platinum, Palladium, Iridium, Osmium, Rhodium and Ruthenium

Supported catalysts palladium, platinum complexes

Supports palladium and platinum

Transition metals Palladium Platinum Rhenium Rhodium

Zerovalent nickel, palladium and platinum

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