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Olins

Multiple bonds in acyclic compounds in bicycloalkanes, tricycloalkanes, and polycycloalkanes, double bonds having priority over triple bonds and in heterocyclic systems whose names end in -etine, -oline, or -olene... [Pg.20]

Olin Corporation Augusta, Ga. 101.6 1965 01in EllF mercury 1... [Pg.480]

Hardness. The hardness (qv), or related property abrasiveness, is an important filler property. Hardness is determined by comparison to materials of known hardness on the Mohs scale. On this nonlinear scale, diamond is rated 10, quartz 7, calcite 3, and talc 1. The abrasiveness of a filler is also dependent on psd and the presence of impurities, eg, ka olin clay (Mohs hardness of 3) can be quite abrasive because of the presence of quartz impurities. [Pg.368]

The simplest was Olin s Thermolia 101, tetrakis(2-chloroethyl) ethylenediphosphate [33125-86-9] C QH2QCl40gP2 (77), used extensively ia flexible foams (78,79). This compound has been discontinued, reportedly because of by-product problems. [Pg.477]

Handbook of Aromatic Fluorine Compounds, Olin Corp., Stamford, Coim., 1976. [Pg.342]

The first large-scale use of hydrazine was as fuel for the rocket-powered German ME-163 fighter plane during World War II. Production in the United States began in 1953 at the Lake Charles, Louisiana plant of the Olin Corp., a facility then having a capacity of 2040 metric tons. In 1992 world capacity was about 44,100 metric tons N2H4. [Pg.273]

MMHa.nd UDMH. MonomethyUiydrazine and yyz -dimethylhydrazine are manufactured by Olin Corp. using the same Raschig process and equipment employed for anhydrous hydrazine. Chloramine, prepared as described above, reacts with methylamine or dimethylamine instead of with... [Pg.282]

The estimated world production capacity for hydrazine solutions is 44,100 t on a N2H4 basis (Table 6). About 60% is made by the hypochlorite—ketazine process, 25% by the peroxide—ketazine route, and the remainder by the Raschig and urea processes. In addition there is anhydrous hydrazine capacity for propellant appHcations. In the United States, one plant dedicated to fuels production (Olin Corp., Raschig process), has a nominal capacity of 3200 t. This facihty also produces the two other hydrazine fuels, monomethyUiydrazine and unsymmetrical dimethyUiydrazine. Other hydrazine fuels capacity includes AH in the PRC, Japan, and Russia MMH in France and Japan and UDMH in France, Russia, and the PRC. [Pg.285]

Oxygen scavengers other than hydrazine are also used, especially catalyzed sodium sulfite, which reacts rapidly with oxygen even at room temperatures to form sodium sulfate. Catalyzed hydrazine formulations are now commercially available that react with oxygen at ambient temperatures at rates comparable to catalyzed sulfite (189). At elevated temperatures, the reaction rates are all similar. Table 14 Hsts the standard hydrazine solution products offered by Olin Corp. for sale to the water-treatment market. Other concentrations are available and other companies offer similar products. [Pg.290]


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See also in sourсe #XX -- [ Pg.642 ]




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