Divided metals

The catalyst is also employed in the form of the finely-divided metal deposited upon activated carbon (usually containing 5 or 10 per cent. Pd) two methods of preparation are described, in one reduction is effected with alkaline formaldehyde solution and in the other with hydrogen ... 

Fluorine is the most electronegative and reactive of all elements. It is a pale yellow, corrosive gas, which reacts with most organic and inorganic substances. Finely divided metals, glass, ceramics, carbon, and even water burn in fluorine with a bright flame. 

Strontium is softer than calcium and decomposes in water more vigorously. It does not absorb nitrogen below 380oC. It should be kept under kerosene to prevent oxidation. Freshly cut strontium has a silvery appearance, but rapidly turns a yellowish color with the formation of the oxide. The finely divided metal ignites spontaneously in air. Volatile strontium salts impart a beautiful crimson color to flames, and these salts are used in pyrotechnics and in the production of flares. Natural strontium is a mixture of four stable isotopes. 

The uncatalyzed addition of hydrogen to an alkene although exothermic is very slow The rate of hydrogenation increases dramatically however m the presence of cer tain finely divided metal catalysts Platinum is the hydrogenation catalyst most often used although palladium nickel and rhodium are also effective Metal catalyzed addi tion of hydrogen is normally rapid at room temperature and the alkane is produced m high yield usually as the only product... 

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... 

Chlorine Ammonia, acetylene, alcohols, alkanes, benzene, butadiene, carbon disulflde, dibutyl phthalate, ethers, fluorine, glycerol, hydrocarbons, hydrogen, sodium carbide, flnely divided metals, metal acetylides and carbides, nitrogen compounds, nonmetals, nonmetal hydrides, phosphorus compounds, polychlorobi-phenyl, silicones, steel, sulfldes, synthetic rubber, turpentine... 

Perchlorates Carbonaceous materials, flnely divided metals particularly magnesium and aluminum, sulfur, benzene, oleflns, ethanol, sulfur, sulfuric acid... 

The first process utilizes a bed of nickel catalyst which has been regenerated with hydrogen to reduce the nickel content to metallic form. The finely divided metal then reacts with impurities and retains them in the bed, probably as nickel oxide in the case of oxygen or as physisorbed compounds for other impurities. Periodically, the bed is regenerated at elevated temperature using hydrogen to restore the metallic content. The nickel process can be used and regenerated indefinitely. 

Slip casting of metal powders closely follows ceramic slip casting techniques (see Ceramics). SHp, which is a viscous Hquid containing finely divided metal particles in a stable suspension, is poured into a plaster-of-Paris mold of the shape desired. As the Hquid is absorbed by the mold, the metal particles are carried to the wall and deposited there. This occurs equally in all directions and equally for metal particles of all sizes which gives a uniformly thick layer of powder deposited at the mold wall. 

Ghalcogenides. Several sulfides are known, but only PuS has been studied ia detail. It is best produced by vacuum decomposition of PuH to finely divided metal at 400°C, followed by reaction with H2S, vacuum decomposition, and re-reaction with H2S several times. It is not attacked by H2O up... 

Stannic Oxide. Stannic oxide tin(IV) oxide, white crystals, mol wt 150.69, mp > 1600° C, sp gr 6.9, is insoluble in water, methanol, or acids but slowly dissolves in hot, concentrated alkaH solutions. In nature, it occurs as the mineral cassiterite. It is prepared industrially by blowing hot air over molten tin, by atomizing tin with high pressure steam and burning the finely divided metal, or by calcination of the hydrated oxide. Other methods of preparation include treating stannic chloride at high temperature with steam, treatment of granular tin at room temperature with nitric acid, or neutralization of stannic chloride with a base. 

In this method, a metal oxide or hydroxide is slurried in an organic solvent, neodecanoic acid is slowly added, and the mixture is refluxed to remove the water. Salts that are basic can be prepared by using less than stoichiometric amounts of acid. This method has been used in the preparation of metal salts of silver (80) and vanadium (81). The third method of preparation is similar to the fusion process, the difference is the use of finely divided metal as the starting material instead of the metal oxide or hydroxide. This method has been appHed to the preparation of cobalt neodecanoate (82). Salts of tin (83) and antimony (84) have been prepared by the fusion method, starting with lower carboxyHc acids, then replacing these acids with neodecanoic acid. 

Cost. The catalytically active component(s) in many supported catalysts are expensive metals. By using a catalyst in which the active component is but a very small fraction of the weight of the total catalyst, lower costs can be achieved. As an example, hydrogenation of an aromatic nucleus requires the use of rhenium, rhodium, or mthenium. This can be accomplished with as fittie as 0.5 wt % of the metal finely dispersed on alumina or activated carbon. Furthermore, it is almost always easier to recover the metal from a spent supported catalyst bed than to attempt to separate a finely divided metal from a liquid product stream. If recovery is efficient, the actual cost of the catalyst is the time value of the cost of the metal less processing expenses, assuming a nondeclining market value for the metal. Precious metals used in catalytic processes are often leased. 

Catalysts vary both in terms of compositional material and physical stmcture (18). The catalyst basically consists of the catalyst itself, which is a finely divided metal (14,17,19) a high surface area carrier and a support stmcture (see Catalysts, supported). Three types of conventional metal catalysts are used for oxidation reactions single- or mixed-metal oxides, noble (precious) metals, or a combination of the two (19). 

Many finely divided metal powders in suspension in air are potential e] losion hazards, and causes for ignition of such dust clouds are numerous [Hartmann and Greenwald, Min. MetalL, 26, 331 (1945)]. Concentration of the dust in air and its particle size are important fac tors that determine explosibility. Below a lower Umit of concentration, no explosion can result because the heat of combustion is insufficient to propagate it. Above a maximum limiting concentration, an explosion cannot be produced because insufficient oxygen is available. The finer the particles, the more easily is ignition accomplished and the more rapid is the rate of combustion. This is illustrated in Fig. 20-7. 

In this article, we will discuss the use of physical adsorption to determine the total surface areas of finely divided powders or solids, e.g., clay, carbon black, silica, inorganic pigments, polymers, alumina, and so forth. The use of chemisorption is confined to the measurements of metal surface areas of finely divided metals, such as powders, evaporated metal films, and those found in supported metal catalysts. 

The rates of gas-solid reaetions are surfaee area dependent, so finely-divided metals, eoal ete. may be prone to oxidation leading to spontaneous eombustion. A eombustible dust will burn mueh more rapidly than the bulk sold, and if dispersed in air eause a dust explosion (refer to Table 6.2). 

Ammonia, acetylene, butadiene, butane or other petroleum gases, sodium carbide, turpentine, benzene, or finely-divided metals Water... 

Segregate stoeks of ehlorine from aeetylene, hydrogen, ammonia and fuel gases and ensure no aeeidental eontaet with ethers, hydroearbons and other organies and finely divided metals. Never mix ehlorine with another gas in the eylinder. 

Chemical Reactivity - Reactivity with Water No reaction Reactivity with Common Materials When mixed with combustible materials or finely divided metals, can become explosive Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. 

Gattermann s Method.— Accoiding to this method the diazonium bromide is first picparcd and then decomposed by finely divided metallic copper. The 50 grams /-toluidine is dissohed in 200 c.c. liydrobromic acid previously diluted with too c.c. water and diazoliscd in the usual way. To this solution... 

The phenol is reduced with hydrogen in presence of finely divided metallic nickel which acts as a catalyst. The apparatus is shown in Fig. 79. 

Two other factors are noteworthy the deleterious effects on chemical and mechanical properties of small amounts of impurities residual from extraction of the metal, and its toxicity. The first of these factors is obviated by vacuum melting the raw metal (for purification) as an essential prerequisite to further processing. The toxicity of beryllium is essentially a pulmonary problem and great care must be taken in handling the finely divided metal or its compounds. In practice, this type of activity is usually carried out under well-ventilated conditions. Certain tolerance levels for atmospheric beryllium are now internationally accepted and merit careful study before work on beryllium is embarked upon. 

Investigation into the effect has been mainly devoted to reactions with red fuming nitric acid . It seems that in red fuming nitric acid a preliminary reaction results in the formation of a surface deposit of finely divided metallic titanium ignition or pyrophoricity can then be initiated by any slight impact or friction. The tendency to pyrophoricity increases as the nitrogen dioxide content of the nitric acid rises from zero to maximum solubility at about 20%, but decreases as the water content rises, the effect being nearly completely stifled at about 2% water. 

Fig. 14-15. X-Ray diffraction patterns of finely divided metallic copper, aluminum, and...

SwedP42115 (1917) CA 11, 2154 (1917) (Expls prepd by mixing alkali or Amm perchlorates with finely divided metallic Zn and combustible non-nitrogenous compds that are not reduced by Zn) 3) Colver (19l8), 286, 680 684 689 4) Barnett (1919), 112-13... 

There are three main types of pyrophoric agents white phosphorus and other inorganic non metals, finely divided metals, and certain organometallic compds... 

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