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X-a-GAL

The most extensive worldwide program on methanol blend gasoline was in Italy where from 1982 to 1987 a 1.9 x lO" m /yr (5 x 10 gal/yr) plant produced a mixture containing 69% methanol. The balance contained higher alcohols. This mixture was blended into gasoline at the 4.3% level and marketed successfully as a premium gasoline known as Super E (82). [Pg.88]

Storage. For receiving glycerol from standard 30.3-m (8000-gal) tank cars (36.3-t), a storage tank of 38—45-m ((10-12) x 10 — gal) capacity should be employed. Preferably it should be of stainless steel (304 or 316), of stainless- or nickel-clad steel, or of aluminum. Certain resin linings such as Lithcote have also been used. Glycerol does not seriously corrode steel tanks at room temperature but gradually absorbed moisture may have an effect. Therefore, tanks should be sealed with an air-breather trap. [Pg.349]

Older rerefining units used 2-5 kg/L of activated clay at 40—70°C and higher temperatures in place of TEE to clean the oil (80). More elaborate chemical and hydrotreating of used engine oils without a distillation step has been developed by Phillips Petroleum for processing 40,000 /yr (10 X 10 gal/yr). Establishment of a reflable feedstock supply is a critical consideration for larger rerefining plants. [Pg.256]

In contrast to predictions of eventual exhaustion of high grade domestic ores of many common metals, seawater is a virtually unlimited source of magnesium. It has been estimated that 1.306 x 10 metric tons of magnesium are present in each cubic kilometer (2.6 x 10 gal) of seawater and there is an estimated 1.3 x 10 km (3.4 x 10 ° gal) of seawater on earth (3). [Pg.313]

Many redundant safety features were provided at the SRP. These included a moderator dump tank, gadolinium nitrate solution as emergency absorber, continuously mnning diesel generators, and a 95 x 10 -L (25 x 10 -gal) elevated water tank for each reactor, for assurance of cooling. [Pg.219]

Vinyltoluene. Viayltoluene is produced by Dow Chemical Company and is used as a resia modifier ia unsaturated polyester resias. Its manufacture is similar to that of styrene toluene is alkylated with ethylene, and the resulting ethyltoluene is dehydrogenated to yield vinyltoluene. Annual production is ia the range of 18,000—23,000 t/yr requiring 20,000—25,000 t (6-7.5 x 10 gal) of toluene. [Pg.192]

The toluenesulfonic acid prepared as an iatermediate ia the preparation ofpara-cmso also has a modest use as a catalyst for various esterifications and condensations. Sodium salts of the toluenesulfonic acids are also used ia surfactant formulations. Annual use of toluene for sulfonation is ca 100,000-150,000 t (30-45 x 10 gal). [Pg.192]

Benzaldehyde. Annual production of ben2aldehyde requires ca 6,500—10,000 t (2-3 x 10 gal) of toluene. It is produced mainly as by-product during oxidation of toluene to benzoic acid, but some is produced by hydrolysis of ben2al chloride. The main use of ben2aldehyde is as a chemical intermediate for production of fine chemicals used for food flavoring, pharmaceuticals, herbicides, and dyestuffs. [Pg.192]

Ethanol s use as a chemical iatemiediate (Table 8) suffered considerably from its replacement ia the production of acetaldehyde, butyraldehyde, acetic acid, and ethyUiexanol. The switch from the ethanol route to those products has depressed demand for ethanol by more than 300 x 10 L (80 x 10 gal) siace 1970. This decrease reflects newer technologies for the manufacture of acetaldehyde and acetic acid, which is the largest use for acetaldehyde, by direct routes usiag ethylene, butane (173), and methanol. Oxo processes (qv) such as Union Carbide s Low Pressure Oxo process for the production of butanol and ethyUiexanol have totaUy replaced the processes based on acetaldehyde. For example, U.S. consumption of ethanol for acetaldehyde manufacture declined steadily from 50% ia 1962 to 37% ia 1964 and none ia 1990. Butadiene was made from ethanol on a large scale duriag World War II, but this route is no longer competitive with butadiene derived from petroleum operations. [Pg.415]

X. Chen, Z.-Y. Liu, J.-B. Zhang, W. Zheng, P. Kowal, and P. G. Wang, Reassembled biosynthetic pathway for large-scale carbohydrate synthesis a-Gal epitope producing superbug, ChemBioChem, 3 (2002) 47-53. [Pg.388]


See other pages where X-a-GAL is mentioned: [Pg.136]    [Pg.142]    [Pg.72]    [Pg.72]    [Pg.79]    [Pg.72]    [Pg.72]    [Pg.79]    [Pg.136]    [Pg.142]    [Pg.72]    [Pg.72]    [Pg.79]    [Pg.72]    [Pg.72]    [Pg.79]    [Pg.226]    [Pg.1]    [Pg.174]    [Pg.188]    [Pg.33]    [Pg.49]    [Pg.224]    [Pg.11]    [Pg.220]    [Pg.64]    [Pg.148]    [Pg.143]    [Pg.75]    [Pg.1]    [Pg.421]    [Pg.228]    [Pg.515]    [Pg.263]    [Pg.124]    [Pg.174]    [Pg.188]    [Pg.65]    [Pg.67]    [Pg.119]    [Pg.120]   
See also in sourсe #XX -- [ Pg.72 , Pg.73 , Pg.74 , Pg.75 , Pg.79 ]

See also in sourсe #XX -- [ Pg.72 , Pg.73 , Pg.74 , Pg.75 , Pg.79 ]




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