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Carbon forms

The corrosion rate of steel in carbonic acid is faster than in hydrochloric acid Correlations are available to predict the rate of steel corrosion for different partial pressures of CO2 and different temperatures. At high temperatures the iron carbonate forms a film of protective scale on the steel s surface, but this is easily washed away at lower temperatures (again a corrosion nomogram is available to predict the impact of the scale on the corrosion rate at various CO2 partial pressures and temperatures). [Pg.94]

Carbon forms a number of oxides in addition to carbon monoxide and dioxide but they are beyond the scope of this book. [Pg.185]

When carbon forms four covalent bonds with halogen atoms the second quantum level on the carbon is completely filled with electrons. Most of the reactions of the Group IV tetrahalides require initial donation by a Lewis base (p. 91) (e.g. water, ammonia) which attaches initially to the tetrahalide by donation of its electron pair. Hence, although the calculated free energy of a reaction may indicate that the reaction is energetically favourable, the reaction may still not proceed. Thus we find that the tetrahalides of carbon... [Pg.195]

Molten Carbonate Fuel Cell. The electrolyte ia the MCFC is usually a combiaation of alkah (Li, Na, K) carbonates retaiaed ia a ceramic matrix of LiA102 particles. The fuel cell operates at 600 to 700°C where the alkah carbonates form a highly conductive molten salt and carbonate ions provide ionic conduction. At the operating temperatures ia MCFCs, Ni-based materials containing chromium (anode) and nickel oxide (cathode) can function as electrode materials, and noble metals are not required. [Pg.579]

The proposed mechanism for producing ethanol [64-17-5] from butane involves -scission of a j -butoxy radical (eq. 38). The j -butoxy radicals are derived from j -butylperoxy radicals (reaction 14 (213)) and/or through some sequence involving reaction 33. If 25% of the carbon forms ethanol, over 50% must pass through the j -butoxy radical. Furthermore, the principal fate of j -butoxy radicals must be the P-scission reaction the ethoxy radical, on the other hand, must be converted to ethanol efficiently. [Pg.343]

The water—carbon slurry formed in the quench vessel is separated from the gas stream and flows to the carbon recovery system needed for environmental reasons and for better thermal efficiency. The recovered carbon is recycled to the reactor dispersed in the feedstock. If the fresh feed does not have too high an ash content, 100% of the carbon formed can be recycled to extinction. [Pg.423]

Travertine is a calcium carbonate formed by chemical precipitation from natural hot-water mineral springs. In appearance and use it is closely akin to... [Pg.164]

Normal, hydrated, and the basic magnesium carbonates react with acids to yield salts which can be recovered by crystallization (43). Magnesium carbonate forms many double salts, some of which are Hsted ia Table 5. [Pg.342]

The solvent, a solution of either sulfuric acid or sodium carbonate, forms the stable complex uranyl ions U02(S04) "2) U02(SO ) )... [Pg.172]

Nickel Fluoroborate. Fluoroboric acid and nickel carbonate form nickel fluoroborate [14708-14-6] Ni(BF 2 6H20. Upon crystallization, the high purity product is obtained (47). Nickel fluoroborate is used as the electrolyte ia specialty high speed nickel plating. It is available commercially as a concentrated solution. [Pg.11]

Some companies have used the Merseburg process to manufacture ammonium sulfate from gypsum, but the process is only economically attractive where sulfur is unavailable or very expensive (32), and is thus not used in the United States. Ammonium carbonate, formed by the reaction of ammonia and carbon dioxide in an aqueous medium, reacts with suspended, finely ground gypsum. Insoluble calcium carbonate and an ammonium sulfate solution are formed. [Pg.368]

Silicon (3), which resembles metals in its chemical behavior, generally has a valence of +4. In a few compounds it exhibits a +2 valence, and in silicides it exists as a negative ion and largely violates the normal valency rules. Silicon, carbon, germanium, tin, and lead comprise the Group 14 (IVA) elements. Silicon and carbon form the carbide, SiC (see Carbides). Silicon and germanium are isomorphous and thus mutually soluble in all proportions. Neither tin nor lead reacts with silicon. Molten silicon is immiscible in both molten tin and molten lead. [Pg.525]

Boron and carbon form one compound, boron carbide [12069-32-8] B C, although excess boron may dissolve ia boron carbide, and a small amount of boron may dissolve ia graphite (5). Usually excess carbon appears as graphite, except for the special case of boron diffused iato diamonds at high pressures and temperatures, eg, 5 GPa (50 kbar) and 1500°C, where boron may occupy both iaterstitial and substitutional positions ia the diamond lattice, a property utilized ia synthetic diamonds (see Carbon, diamond, synthetic). [Pg.219]

Carbon Composites. In this class of materials, carbon or graphite fibers are embedded in a carbon or graphite matrix. The matrix can be formed by two methods chemical vapor deposition (CVD) and coking. In the case of chemical vapor deposition (see Film deposition techniques) a hydrocarbon gas is introduced into a reaction chamber in which carbon formed from the decomposition of the gas condenses on the surface of carbon fibers. An alternative method is to mold a carbon fiber—resin mixture into shape and coke the resin precursor at high temperatures and then foUow with CVD. In both methods the process has to be repeated until a desired density is obtained. [Pg.275]

Hydroxyhc Compounds. Chloioformates on reaction with water give the patent hydroxy compound, HCl, and CO2 as weU as the symmetrical carbonate formed by the reaction of the hydroxy compound with chloroformate. [Pg.38]

Surface oxidation short of combustion, or using nitric acid or potassium permanganate solutions, produces regenerated humic acids similar to those extracted from peat or soil. Further oxidation produces aromatic acids and oxaUc acid, but at least half of the carbon forms carbon dioxide. [Pg.224]

Mechanical properties depend on the alloying elements. Addition of carbon to the cobalt base metal is the most effective. The carbon forms various carbide phases with the cobalt and the other alloying elements (see Carbides). The presence of carbide particles is controlled in part by such alloying elements such as chromium, nickel, titanium, manganese, tungsten, and molybdenum that are added during melting. The distribution of the carbide particles is controlled by heat treatment of the solidified alloy. [Pg.372]

Sodium chloride and sodium cyanide are isomorphous and form an unintermpted series of mixed crystals. The ferrocyanide ion has a marked effect on the habit of sodium cyanide crystallized from aqueous solution (50). Sodium cyanide and sodium carbonate form a molten eutectic at approximately 53 wt % sodium carbonate and 465°C. The specific conductivity of molten 98% sodium cyanide is 1.17 S /cm (51). [Pg.381]

Carbon blacks are synthetic materials which essentially contain carbon as the main element. The structure of carbon black is similar to graphite (hexagonal rings of carbon forming large sheets), but its structure is tridimensional and less ordered. The layers of carbon blacks are parallel to each other but not arranged in order, usually forming concentric inner layers (turbostratic structure). Some typical properties are density 1.7-1.9 g/cm pH of water suspension 2-8 primary particle size 14-250 nm oil absorption 50-300 g/100 g specific surface area 7-560 m /g. [Pg.636]


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Allotropic forms of carbon

Calcium carbonate natural forms

Carbon Bond-Forming Reactions of Organoboranes

Carbon Bonding-Forming Reactions in Organic Synthesis

Carbon Double Bond Forming Reactions

Carbon allotropic forms

Carbon as Structure-Forming Element in Porous Fuel Cell Electrodes

Carbon bond-forming reactions

Carbon chain-forming properties

Carbon dioxide amorphous solid form

Carbon dioxide formed from uric acid

Carbon elemental forms

Carbon emission, forms

Carbon forming reactions

Carbon forms, production

Carbon fullerenes allotropic forms

Carbon heteroatom bond forming reactions aminals, formation

Carbon hydrogen bond forming reactions

Carbon hydrogen bond forming reactions hydrogenation

Carbon in the form of carbonate ions

Carbon many forms

Carbon novel forms

Carbon polymorphic forms

Carbon properties of crystalline forms

Carbon reference form

Carbon standard elemental form

Carbon tested forms

Carbon, fixed forms

Carbon, fixed forms radioactive

Carbon- and water-based life forms

Carbon-Heteroatom Bond forming Processes

Carbon-Heteroatom Bond-Forming or Cleaving Reactions

Carbon-Heteroelement Bond-Forming Reactions

Carbon-boron bond forming reactions

Carbon-fluorine bond forming reactions

Carbon-fluorine bond forming reactions alkenes

Carbon-forming propensity

Carbon-halogen bond forming reactions

Carbon-heteroatom bond forming

Carbon-heteroatom bond forming reactions

Carbon-iodine bond forming reactions

Carbon-nitrogen bond forming reactions Michael addition

Carbon-nitrogen bond forming reactions cyclization

Carbon-nitrogen bond forming reactions intramolecular cyclization

Carbon-nitrogen bond forming reactions ketones

Carbon-nitrogen bond forming reactions oxidative cyclization

Carbon-nitrogen bond forming reactions reaction

Carbon-nitrogen bond forming reactions reductive-cyclization

Carbon-nitrogen bond-forming reactions

Carbon-oxygen bond forming reactions

Carbon-phosphorus bond forming reactions

Carbon-sulfur bond-forming reactions

Carbonic acid forms

Carbons forms, mechanical properties

Carbon—sulfur bond forming reactions formation

Conductivity in Allotropic Forms of Carbon

Conversion into Other Forms of Carbon

Crystalline forms of carbon

Different Forms of Carbon

Elemental Forms of Carbon

Elimination reactions forming carbon-oxygen double bonds with

Eliminations to Form Carbon-Oxygen Double Bonds Oxidation Reactions

Forming Carbon Dioxide

Forms of Carbons Deposits

Forms of carbon

Gaseous Forms of Carbon

High-surface-area active carbon formed

Ligands forming metal-carbon multiple bonds

Ligands forming several metal-carbon single

Miscellaneous Carbon-Heteroatom Bond-Forming Reactions

New Forms of Carbon

OTHER FORMS OF CARBON AND GRAPHITE

Other Forms of Carbon

Palladium-Catalyzed Carbon-Heteroatom Bond Forming Reactions

Reactions in which carbon-cobalt bonds are formed

Solid Ceo A New Form of Carbon

Solid forming component, carbon

Structure of a-Class Carbonic Anhydrase from Human Erythrocytes (the High Activity form HCA II)

Synthesis of Alkylamines and Related Compounds through Nitrogen-Carbon(sp3) Bond-Forming Reactions

Synthesis of Ynamides and Related Compounds through Nitrogen-Carbon(sp) Bond-Forming Reactions

The Forms of Carbon

Types of bonds formed by the carbon atom

VGCFs, carbon nanotubes form

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