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Alumina chlorided

CYCLOADDITION Alumina chloride. l,2-Bis(trimethylsilyloxy)cyclo-butene. 2,2-Dimcthyl-3(2//)-furanone. Lthylaluminum dichloridc. Kctcnc diethyl acetal.. Methyl cyclobutene-carboxylate. Trimethyl-1,3-dioxolen-one. Zinc chloride. [Pg.466]

Alumina, chlorided alumina, Laser Raman spectra of chemisorbed 60... [Pg.121]

Alumina sulfate TR-Bond PLOT, Alumina Alumina chloride PLOT (Na SO /KOI)... [Pg.135]

Surface heterogeneity may be inferred from emission studies such as those studies by de Schrijver and co-workers on P and on R adsorbed on clay minerals [197,198]. In the case of adsorbed pyrene and its derivatives, there is considerable evidence for surface mobility (on clays, metal oxides, sulfides), as from the work of Thomas [199], de Mayo and co-workers [200], Singer [201] and Stahlberg et al. [202]. There has also been evidence for ground-state bimolecular association of adsorbed pyrene [66,203]. The sensitivity of pyrene to the polarity of its environment allows its use as a probe of surface polarity [204,205]. Pyrene or ofter emitters may be used as probes to study the structure of an adsorbate film, as in the case of Triton X-100 on silica [206], sodium dodecyl sulfate at the alumina surface [207] and hexadecyltrimethylammonium chloride adsorbed onto silver electrodes from water and dimethylformamide [208]. In all cases progressive structural changes were concluded to occur with increasing surfactant adsorption. [Pg.418]

Dioxan develops appreciable quantities of peroxides upon exposure to air or upon keeping. These can be eliminated by refluxing over anhydrous stannous chloride (compare Section VI, 12) or by filtration through a column of activated alumina. [Pg.177]

Aryl, heteroaryl, and alkenyl cyanides are prepared by the reaction of halides[656-658] or triflates[659,660] with KCN or LiCN in DMF, HMPA, and THF. Addition of crown ethers[661] and alumina[662] promotes efficient aryl and alkenyl cyanation. lodobenzene is converted into benzonitrile (794) by the reaction of trimethylsiiyl cyanide in EtiN as a solvent. No reaction takes place with aryl bromides and chlorides[663]. The reaction was employed in an estradiol synthesis. The 3-hydroxy group in 796 was derived from the iodide 795 by converting it into a cyano group[664]. [Pg.246]

In liquid-solid adsorption chromatography (LSC) the column packing also serves as the stationary phase. In Tswett s original work the stationary phase was finely divided CaCOa, but modern columns employ porous 3-10-)J,m particles of silica or alumina. Since the stationary phase is polar, the mobile phase is usually a nonpolar or moderately polar solvent. Typical mobile phases include hexane, isooctane, and methylene chloride. The usual order of elution, from shorter to longer retention times, is... [Pg.590]

Alumina trihydtate is also used as a secondary flame retardant and smoke suppressant for flexible poly(vinyl chloride) and polyolefin formulations in which antimony and a halogen ate used. The addition of minor amounts of either zinc borate or phosphoms results in the formation of glasses which insulate the unbumed polymer from the flame (21). [Pg.458]

Alumina Trihydrate. Alumina trihydrate is usually used as a secondary flame retardant in flexible PVC because of the high concentration needed to be effective. As a general rule the oxygen index of flexible poly(vinyl chloride) increases 1% for every 10% of alumina trihydrate added. The effect of alumina trihydrate on a flexible poly(vinyl chloride) formulation containing antimony oxide is shown in Figure 5. [Pg.461]

There are several processes available for the manufacture of cryoHte. The choice is mainly dictated by the cost and quaUty of the available sources of soda, alumina, and fluoriae. Starting materials iaclude sodium aluminate from Bayer s alumina process hydrogen fluoride from kiln gases or aqueous hydrofluoric acid sodium fluoride ammonium bifluoride, fluorosiUcic acid, fluoroboric acid, sodium fluosiUcate, and aluminum fluorosiUcate aluminum oxide, aluminum sulfate, aluminum chloride, alumina hydrate and sodium hydroxide, sodium carbonate, sodium chloride, and sodium aluminate. [Pg.144]

By-product water formed in the methanation reactions is condensed by either refrigeration or compression and cooling. The remaining product gas, principally methane, is compressed to desired pipeline pressures of 3.4—6.9 MPa (500—1000 psi). Einal traces of water are absorbed on siHca gel or molecular sieves, or removed by a drying agent such as sulfuric acid, H2SO4. Other desiccants maybe used, such as activated alumina, diethylene glycol, or concentrated solutions of calcium chloride (see Desiccants). [Pg.75]

Natural gas contains both organic and inorganic sulfur compounds that must be removed to protect both the reforming and downstream methanol synthesis catalysts. Hydrodesulfurization across a cobalt or nickel molybdenum—zinc oxide fixed-bed sequence is the basis for an effective purification system. For high levels of sulfur, bulk removal in a Hquid absorption—stripping system followed by fixed-bed residual clean-up is more practical (see Sulfur REMOVAL AND RECOVERY). Chlorides and mercury may also be found in natural gas, particularly from offshore reservoirs. These poisons can be removed by activated alumina or carbon beds. [Pg.276]

In 1976 the first section of a new smelting process that requited 30% less electric power than the best Hah-HAroult cehs came on stream. In this process, alumina, carbon, and chlorine reacted to produce aluminum chloride and carbon dioxide. The aluminum chloride was electrolyzed in bipolar electrode cehs to produce aluminum and chlorine and the chlorine was recycled to make more aluminum chloride. After six years of operation, the plant... [Pg.100]

Anhydrous aluminum chloride, AIQ, is manufactured primarily by reaction of chlorine [7782-50-5] vapor with molten aluminum and used mainly as a catalyst in organic chemistry ie, in Friedel-Crafts reactions (qv) and in proprietary steps in the production of titanium dioxine [13463-67-7] Ti02, pigment. Its manufacture by carbochlorination of alumina or clay is less energy-intensive and is the preferred route for a few producers (19). [Pg.136]

Both the Toth and Alcoa processes provide aluminum chloride for subsequent reduction to aluminum. Pilot-plant tests of these processes have shown difficulties exist in producing aluminum chloride of the purity needed. In the Toth process for the production of aluminum chloride, kaolin [1332-58-7] clay is used as the source of alumina (5). The clay is mixed with sulfur and carbon, and the mixture is ground together, pelletized, and calcined at 700°C. The calcined mixture is chlorinated at 800°C and gaseous aluminum chloride is evolved. The clay used contains considerable amounts of silica, titania, and iron oxides, which chlorinate and must be separated. Silicon tetrachloride and titanium tetrachloride are separated by distillation. Resublimation of aluminum chloride is requited to reduce contamination from iron chloride. [Pg.147]

The large majority of activated alumina products are derived from activation of aluminum hydroxide, rehydrated alumina, or pseudoboehmite gel. Other commerical methods to produce specialty activated aluminas are roasting of aluminum chloride [7446-70-0], AIQ calcination of precursors such as ammonium alum [7784-25-0], AlH2NOgS2. Processing is tailored to optimize one or more of the product properties such as surface area, purity, pore size distribution, particle size, shape, or strength. [Pg.155]

Chlorides may be found in natural gas, particularly associated with offshore reservoirs. Modified alumina catalysts have been developed to irreversibly absorb these poisons from the feed gas. [Pg.346]

Many forms of chromatography have been used to separate mixtures of quinoline and isoquinoline homologues. For example, alumina saturated with cobalt chloride, reversed-phase Hquid chromatography, and capillary gas chromatography (gc) with deactivated glass columns have all been employed (38,39). [Pg.390]


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See also in sourсe #XX -- [ Pg.126 , Pg.127 , Pg.128 , Pg.129 ]




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