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G-acid

If a catalyst is to work well in solution, it (and tire reactants) must be sufficiently soluble and stable. Most polar catalysts (e.g., acids and bases) are used in water and most organometallic catalysts (compounds of metals witli organic ligands bonded to tliem) are used in organic solvents. Some enzymes function in aqueous biological solutions, witli tlieir solubilities detennined by the polar functional groups (R groups) on tlieir outer surfaces. [Pg.2700]

Hydroxamic acid formation resembles amide formation (pp. 117-119) and therefore certain other classes of substances will respond to the test, e.g., acid chlorides and acid anhydrides, but these substances are readily distinguished by other reactions. [Pg.334]

Sodium and potassium hydroxides. The use of these efficient reagents is generally confined to the drying of amines (soda lime, barium oxide and quicklime may also be employed) potassium hydroxide is somewhat superior to the sodium compound. Much of the water may be first removed by shaking with a concentrated solution of the alkali hydroxide. They react with many organic compounds (e.g., acids, phenols, esters and amides) in the presence of water, and are also soluble in certain organic liquids so that their use as desiccants is very limited... [Pg.142]

Spherical, pentagonal dodecahedrane is the thermodynamically most stable CjoHjo-polycycloalkane. It is the so-called CjjHjo stabilomer . It should therefore be available by thermod5mamically controlled, e.g. acid-catalyzed, isomerization of less stable C24H20-isomers. Experiments along this line, e.g. treatment of the basketene photo-dimer with Lewis... [Pg.334]

Acid Deposition. Acid deposition, the deposition of acids from the atmosphere to the surface of the earth, can be dry or wet. Dry deposition involves acid gases or their precursors or acid particles coming in contact with the earth s surface and thence being retained. The principal species associated with dry acid deposition are S02(g), acid sulfate particles, ie, H2SO4 and NH HSO, and HN02(g). Measurements of dry deposition are quite sparse, however, and usually only speciated as total and total NO3. In general, dry acid deposition is estimated to be a small fraction of the total... [Pg.377]

Other disazo dyes with good substantivity and high wet-fastness properties on polyamides are Acid Red 114 (40), made by coupling o-toHdine to phenol which is then coupled to G-acid, followed by reaction of the phenoHc hydroxyl group with -toluenesulfonyl chloride, and Acid Blue 113 (41) (metanilic acid — 1-naphthylamine — 8-anilino-1-naphthalenesulfonic acid). [Pg.435]

Acid DEG, mol/mol acid IR-120, g/100 g acid Temp, °C Reaction time, h Monoester, % conv Diester, % conv... [Pg.376]

Corrosion Probiems in Service. The wide variety of corrosive factors that are present in refining and petrochemical processing (e.g., acids, caustics, chlorides, sulfides, sulfates) give rise to a wide variety of corrosive attacks, some of which act ... [Pg.250]

Thermal degradation in contact with flame or red hot surfaces will produce highly-toxic gases, e.g. acid chlorides and phosgene. Reaction with freshly-galvanized surfaces may produce dichloroacetylene, which is also highly toxic. [Pg.139]

Decomposition of trichloroethylene can occur upon contact with naked flames, red-hot surfaces, hot elements of electric heaters, or intense UV light with the generation of acidic and highly-toxic products. The presence of reactive contaminants, e.g. acids, strong alkalis, highly-reactive metals, may also result in decomposition to similar products. [Pg.141]

Technology Description Hydrolysis is the process of breaking a bond in a molecule (which is ordinarily not water-soluble) so that it will go into ionic solution with water. Hydrolysis can be achieved by the addition of chemicals (e.g., acid hydrolysis), by irradiation (e.g., photolysis) or by biological action (e.g., enzymatic bond cleavage). The cloven molecule can then be further treated by other means to reduce toxicity. [Pg.148]

Take care when a hazardous substance (e.g. acid) is lifted. [Pg.1063]

Wood is particularly valuable for many conditions which are corrosive to common metals (e.g. acids and external exposure), and for contact with foodstuffs and beverages. It is not subject to corrosion in the electrochemical sense of the term applied to metals, but in saline conditions it can be attacked by the products of metal corrosion (alkali and iron salts) where poor technology or unsuitable wood species are used. Although wood is attacked by both extremely alkaline and acid conditions, particularly those which are oxidising, it can be employed over a wider pH range than most other materials. [Pg.957]

Thorium oxide on activated carbon was prepared by absorption of thorium nitrate from its solution in anhydrous acetone on the activated carbon Supersorbon. The excess solution was decanted, the catalyst was dried at 80 °C, and the adsorbed thorium oxide was decomposed by excess 5% ammonium hydroxide solution. After repeated washing and decanta-nation with distilled water and acetone, the catalyst was dried at 180°C. It was then stabilized by heating to 360°C for 5 hr in a stream of nitrogen. The content of thorium oxide was 2.9% (wt.). The BET surface area was 870 m2/g. Prior to kinetic measurements, the catalyst was modified by passing over acetic acid vapors (100 g acid/1 g catalyst). [Pg.27]

Lynch-Stewart, P. Wiken, E.B. Ironside, G. Acid Deposition on Prime Resource Lands in Eastern Canada, Canada Land Inventory Rept, No. 18, Lands Directorate, Environment Canada, Ottawa, Ontario, 1987. [Pg.62]


See other pages where G-acid is mentioned: [Pg.87]    [Pg.76]    [Pg.527]    [Pg.249]    [Pg.850]    [Pg.9]    [Pg.43]    [Pg.430]    [Pg.430]    [Pg.430]    [Pg.158]    [Pg.495]    [Pg.501]    [Pg.78]    [Pg.291]    [Pg.291]    [Pg.291]    [Pg.82]    [Pg.21]    [Pg.395]    [Pg.650]    [Pg.128]    [Pg.4]    [Pg.734]    [Pg.220]    [Pg.225]    [Pg.298]    [Pg.197]    [Pg.1065]    [Pg.552]    [Pg.552]    [Pg.110]    [Pg.372]    [Pg.103]    [Pg.114]    [Pg.141]   
See also in sourсe #XX -- [ Pg.555 ]

See also in sourсe #XX -- [ Pg.321 , Pg.324 ]

See also in sourсe #XX -- [ Pg.877 , Pg.884 , Pg.896 ]




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Barker, G, R., Nucleic Acids

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Henning, H. G., Gelbin, A., Advances Tetramic Acid Chemistry

Isodomoic acids G and

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Perchloric Acid G. S. Pearson

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