White catalyst

Similarly, allyhc C-H oxidation can streamline the constraction of oxygenated compounds by reducing functional group manipulations necessary for working with bisoxygenated intermediates. For example, a chiral allylic C-H oxidation/enzymatic resolntion seqnence furnished bisoxygenated compound 14 in 97% ee and in 42% overall yield in jnst 3 steps from a coimnercially available 

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Fig. 28. The cumulative COj/CO ratio for coke bum-off on spherical catalyst beads versus combustion temperature in air (O) white amorphous silica-alumina ( ) green Cr02-containing amorphous silica-alumina (M) macroporous white catalyst. The weight (mg) of the bead tested is denoted by the numerals adjacent to the respective symbol. Dashed line represents intrinsic ratios from carbon combustion research. From Weisz (1966).

Besides the one-pot process described above, the White catalyst catalyzes a chelate-controUed oxidative Heck arylation between a wide range of a-olefins and organoborane compounds in good yields and with excellent regio- and stereoselectivities (Figure 6). Unlike other Heck arylation methods, no Pd-H isomerization is observed under the mild reaction conditions. Aiyl boronic acids, styrenylpinacol boronic esters, and aryl potassium trifluoroborates (activated with boric acid) are aU compatible with the general reaction conditions. 

The sample in Fig. 3(a) is a common eggshell catalyst all the active metal is concentrated on the upper shell of the support grain. As a large grain was used for such a test, it is possible to observe a white heart due to "uncontaminated" alumina. On the contrary, the sonicated sample in Fig. 3(b) is characterized by a black halo due to the ruthenium atoms that migrated inside the support. This kind of catalyst is commonly called egg-white catalyst and is industrially prepared in the presence of citric or tartaric acid. Sonochemically the same result is obtained without using any chemical which could poison the active sites. 

CoAsS, are also used as sources. The ore is roasted and Co is precipitated as the hydroxide and then reduced to Co with carbon (hep below 417 - C, cep to m.p.). The metal is silvery white and readily polished. It dissolves in dilute acids and is slowly oxidized in air. Adsorbs hydrogen strongly. The main use of cobalt is in alloys. Cobalt compounds are used in paints and varnishes, catalysts. Cobalt is an essential element in the diet. World production 1976 32 000 tonnes metal. 

C (Mond process). The silver-white metal is ccp. The metal is not tarnished by air but is attacked by acids (except cone. HNO3). It is resistant to Fj. It is used extensively in alloys, particularly in steels and cast iron and as a coinage metal. Used in glass (green) in catalysts (particularly for hydrogenation). Western world production 1981 662 000 tonnes. 

Ethylene. Under the influence of pressure and a catalyst, ethylene yields a white, tough but flexible waxy sohd, known as Polythene. Polyethylene possesses excellent electric insulation properties and high water resistance it has a low specific gravity and a low softening point (about 110°). The chemical inertness oi Polythene has found application in the manufacture of many items of apparatus for the laboratory. It is a useful lubricant for ground glass connexions, particularly at relatively high temperatures. 

Miscellaneous Reactions. Sodium bisulfite adds to acetaldehyde to form a white crystalline addition compound, insoluble in ethyl alcohol and ether. This bisulfite addition compound is frequendy used to isolate and purify acetaldehyde, which may be regenerated with dilute acid. Hydrocyanic acid adds to acetaldehyde in the presence of an alkaU catalyst to form cyanohydrin the cyanohydrin may also be prepared from sodium cyanide and the bisulfite addition compound. Acrylonittile [107-13-1] (qv) can be made from acetaldehyde and hydrocyanic acid by heating the cyanohydrin that is formed to 600—700°C (77). Alanine [302-72-7] can be prepared by the reaction of an ammonium salt and an alkaU metal cyanide with acetaldehyde this is a general method for the preparation of a-amino acids called the Strecker amino acids synthesis. Grignard reagents add readily to acetaldehyde, the final product being a secondary alcohol. Thioacetaldehyde [2765-04-0] is formed by reaction of acetaldehyde with hydrogen sulfide thioacetaldehyde polymerizes readily to the trimer. 

Boron trifluoride [7637-07-2] (trifluoroborane), BF, was first reported in 1809 by Gay-Lussac and Thenard (1) who prepared it by the reaction of boric acid and fluorspar at duU red heat. It is a colorless gas when dry, but fumes in the presence of moisture yielding a dense white smoke of irritating, pungent odor. It is widely used as an acid catalyst (2) for many types of organic reactions, especially for the production of polymer and petroleum (qv) products. The gas was first produced commercially in 1936 by the Harshaw Chemical Co. (see also Boron COMPOUNDS). 

Thermoplastic resins produced from pure monomers such as styrene, alkyl-substituted styrenes, and isobutylene are produced commercially. An advantage of these resins is the fact that they are typically lighter in color than Gardner 1 (water-white) without being hydrogenated. Among the earliest resins in this category were those made from styrene and sold as Piccolastic. Styrene and alkyl-substituted styrenes such as a-methylstyrene are very reactive toward Friedel-Crafts polymerization catalysts. 

Lead Telluride. Lead teUuride [1314-91 -6] PbTe, forms white cubic crystals, mol wt 334.79, sp gr 8.16, and has a hardness of 3 on the Mohs scale. It is very slightly soluble in water, melts at 917°C, and is prepared by melting lead and tellurium together. Lead teUuride has semiconductive and photoconductive properties. It is used in pyrometry, in heat-sensing instmments such as bolometers and infrared spectroscopes (see Infrared technology AND RAMAN SPECTROSCOPY), and in thermoelectric elements to convert heat directly to electricity (33,34,83). Lead teUuride is also used in catalysts for oxygen reduction in fuel ceUs (qv) (84), as cathodes in primary batteries with lithium anodes (85), in electrical contacts for vacuum switches (86), in lead-ion selective electrodes (87), in tunable lasers (qv) (88), and in thermistors (89). 

Although white lead was the oldest white hiding pigment ia paints, it has been totally replaced by titanium dioxide, which has better covering power and is nontoxic (see Pigments). Nevertheless, basic lead carbonate has many other uses, including as a catalyst for the preparation of polyesters from... 

Nickel Oxalate. This salt, NiC204, mol wt 146.7, is produced as a greenish white crystalline dihydrate [6018-94-6]. It decomposes by heating at 320°C under vacuum into Ni metal and carbon dioxide. Nickel oxalate is used for the production of nickel catalysts and magnetic materials. 

A number of process improvements have been described, and iaclude the use of white mineral oil having a boiling range of 300—400°C (60) or the use of a mixture of cresols (61). These materials act to reduce the reaction mixture s viscosity, thus improving mixing. Higher sebacic acid yields are claimed by the use of catalysts such as barium salts (62), cadmium salts (63), lead oxide, and salts (64). 

Cobalt. Without a doubt cobalt 2-ethyIhexanoate [136-52-7] is the most important and most widely used drying metal soap. Cobalt is primarily an oxidation catalyst and as such acts as a surface or top drier. Cobalt is a transition metal which can exist in two valence states. Although it has a red-violet color, when used at the proper concentration it contributes very Httie color to clear varnishes or white pigmented systems. Used alone, it may have a tendency to cause surface wrinkling therefore, to provide uniform drying, cobalt is generally used in combination with other metals, such as manganese, zirconium, lead, calcium, and combinations of these metals. 

J. J. White, Eow Emission Catalysts for Natural Gas Engines, GRI Report 91/0214, Gas Research Institute, Chicago, Southwest Research Institute, San Antonio, SwRI 3178-22,1991. 

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