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Cobalt naphthalene

Methyl Methacrylate Cumene hydroperoxide Cobalt naphthalenate (6% Co)... [Pg.401]

Unsaturated polyesters are fast-curing, two-part systems that harden by the addition of catalysts, usually peroxides. Styrene monomer is generally used as a reactive diluent for polyester resins. Cure can occur at room or elevated temperature depending on the type of catalyst Accelerators such as cobalt naphthalene are sometimes incorporated into the resin to speed cure. Unsaturated polyester adhesives exhibit greater shrinkage during cure and poorer chemical resistance than epoxy adhesives. Certain types of polyesters are inhibited from curing by the presence of air, but they cure fully when enclosed between two... [Pg.465]

Fluorination of naphthalene in a stream of dilute fluorine over cobalt trifluoride yields a mixture of perfluorodecalins and partially fluorinated naphthalene derivatives that are fully fluorinated to perfluorodecalins by a subsequent treatment with dilute fluorine [23] Perfluorodecalins are also final products ot fluorination of tetralin over cobalt trifluoride at 250 °C. A more thorough investigation of this reacPon revealed seven additional compounds as products and intermediates [//] (equation 6). [Pg.124]

The surface analyses of the Co/MgO catalyst for the steam reforming of naphthalene as a model compound of biomass tar were performed by TEM-EDS and XPS measurements. From TEM-EDS analysis, it was found that Co was supported on MgO not as particles but covering its surface in the case of 12 wt.% Co/MgO calcined at 873 K followed by reduction. XPS analysis results showed the existence of cobalt oxide on reduced catalyst, indicating that the reduction of Co/MgO by H2 was incomplete. In the steam reforming of naphthalene, film-like carbon and pyrolytic carbon were found to be deposited on the surface of catalyst by means of TPO and TEM-EDS analyses. [Pg.517]

Keywords cobalt catalyst, naphthalene, steam reforming, biomass, gasification, tar 1. Introduction... [Pg.517]

Siunova, T., Anokhina, T., Mashukova, A., Kochetkov, V., and Boronin, A., Rhizosphere strain of Pseudomonas chlororaphis capable of degrading naphthalene in the presence of cobalt/nickel, Microbiology, 76 (2), 182-188, 2007. [Pg.428]

Two general approaches have been used to prepare the cobalt powders. The first method(34,37,42) used 2.3 equivalents of lithium along with naphthalene as an electron carrier in DME to reduce anhydrous cobalt chloride to a dark gray powder, L Use of cobalt bromides or iodides gave a... [Pg.235]

Cobalt acetate is used to make acetic acid out of butane palladium chlo-ride/cupric chloride is used to make MEK out of butylene and lo and behold, to make phthalic anhydride out of ortho-xylene or naphthalene, you use vanadium pentoxide. [Pg.433]

In a somewhat different approach, Asahi Glass KK have claimed [132] that the addition of a transition metal salt (e. g., cobalt-, copper-, lead-, cerium-, bismuth-, manganese-, chromium-, iron- chloride, or cobalt fluoride, etc.) greatly improves the ECF production of perfluorobicyclic compounds, derived from naphthalene, indene, benzofuran, phthalimide, indole, quinolizine, benzotriazole, and quinoline. [Pg.226]

The action of carbon tetrachloride or a mixture of chlorine with a hydrocarbon or carbon monoxide on the oxide.—H. N. Warren 9 obtained aluminium chloride by heating the oxide to redness with a mixture of petroleum vapour and hydrogen chloride or chlorine, naphthalene chloride or carbon tetrachloride was also used. The bromide was prepared in a similar manner. E. Demarpay used the vapour of carbon tetrachloride, the chlorides of chromium, titanium, niobium, tantalum, zirconium, cobalt, nickel, tungsten, and molybdenum H. Quantin, a mixture of carbon monoxide and chlorine and W. Heap and E. Newbery, carbonyl chloride. [Pg.216]

Chemicals which can damage (a) the liver include carbon tetrachloride, paracetamol, bromobenzene, isoniazid, vinyl chloride, ethionine, galactosamine, halothane, dimethyl-nitrosamine (b) the kidney include hexachlorobutadiene, cadmium and mercuric salts, chloroform, ethylene glycol, aminoglycosides, phenacetin (c) the lung include paraquat, ipomeanol, asbestos, monocrotaline, sulfur dioxide, ozone, naphthalene (d) the nervous system include MPTP, hexane, organophosphoms compounds, 6-hydroxydopamine, isoniazid (e) the testes include cadmium, cyclophosphamide, phthalates, ethanemethane sulfonate, 1,3-dinitrobenzene (f) the heart include allylamine, adriamycin, cobalt, hydralazine, carbon disulfide (g) the blood include nitrobenzene, aniline, phenyl-hydrazine, dapsone. [Pg.430]

Sumimoto introduced a new sebacic acid process including several catalytic hydrogenation reactions.342 The synthesis starts with naphthalene, which is first partially hydrogenated to tetralin over cobalt oxide or molybdenum oxide, then to decalin over ruthenium or iridium on carbon. The selectivity to cw-decalin is better than 90%. In a later phase of the synthesis 5-cyclododecen-l-one is hydrogenated over Raney nickel to obtain a mixture of cyclododecanone and cyclodode-canol in a combined yield of 90%. The selectivity of this step is not crucial since subsequent oxidation of either compound leads to the endproduct sebacic acid. [Pg.666]

Tricarbonyl(naphthalene)chromium, 19 Trimethylsilyl chlorochromate, 327 Cobalt Compounds Acylcobaltate complexes, 101 [Bis(salicylidene-y-iminopropyl)methyl-amine]cobalt(II), 41 Cobalt(II) chloride, 249 Cobalt zeolites, 296 Dicarbonylcyclopentadienylcobalt, 96 Di- x-carbonylhexacarbonyldicobalt,... [Pg.408]

Besides the direct photoreactions reported to date (see Figure 6.6), coordination entities also undergo the photosensitized modes in which they play the role of non-absorbing substrate. The application is usually connected with solving some mechanistic problems, as in the early study of cobalt(III) complexes with organic sensitizers, such as biacetyl, benzophenone, benzaldehyde, and naphthalene, which provided valuable mechanistic information about the excited states responsible for the photophysical, photoredox, and photosubstitution processes observed in cases of these complexes [105],... [Pg.58]

Figures 1.1 a-c show the relationships between the catalytic activity and the degree of development that have been studied in the hydrogenation of cyclohexanone, naphthalene, and benzene over single phase NiAl3 and Co2A19 alloys. The rates of hydrogenation peak at around 82-86% degrees of development with both the alloys, and tend to decrease markedly with further development, irrespective of the compounds hydrogenated. It is noted that the cobalt catalyst from Co2A19 is... Figures 1.1 a-c show the relationships between the catalytic activity and the degree of development that have been studied in the hydrogenation of cyclohexanone, naphthalene, and benzene over single phase NiAl3 and Co2A19 alloys. The rates of hydrogenation peak at around 82-86% degrees of development with both the alloys, and tend to decrease markedly with further development, irrespective of the compounds hydrogenated. It is noted that the cobalt catalyst from Co2A19 is...
Cobalt catalysts are generally known to be less active than nickel catalysts for the hydrogenation of aromatic compounds (see, e.g., Table 11.2).4,5 However, properly prepared reduced cobalt or Raney Co have been reported to be more active than the corresponding nickel catalysts in the hydrogenation of benzene13-15 and naphthalene.15... [Pg.417]

Amoco Amoco Chemicals Company, a subsidiary of Amoco Corporation, formerly Standard Oil Company (IN), is best known in the chemicals industry for its modification of the Mid-Century process for making pure terephthalic acid. p-Xylene in acetic acid solution is oxidized with air at high temperature and pressure. Small amounts of manganese, cobalt, and bromide are used as catalysts. The modification allows the use of terephthalic acid, rather than dimethyl terephthalate, for making fiber. The process can also be used for oxidizing other methylbenzenes and methyl-naphthalenes to aromatic carboxylic acids. See also Maruzen. [Pg.19]

UNIDAK A process for extracting naphthalene from reformer residues in petroleum refining. It includes a dealkylation stage to convert the naphthalene homologues to naphthalene. The process temperature is approximately 600°C the catalyst is based on cobalt/molybdenum. Developed by the Union Oil Company of California. [Pg.378]

Finely divided cobalt, as obtained from anydrous cobalt halides with Li/naphthalene in glyme, is converted to Co2(CO)g in good yields at 100 °C and 95 atm of pressure. [Pg.644]

Binuclear complexes of naphthalene (VIII) and of benzene (IX) with [Os(NH3)5]2+ and [Ru(NH3)5]2+ moieties were reported by Taube et al. (19), in which anti- //-1,2-rj2 3,4- 2) coordination of the arene is present. This bonding mode was first observed by Pasman et al. (20) in the binuclear Rhenium complex X. Wolczanski et al. (21) obtained complex XI from the mononuclear complex [Ta(0—Si Bu3)3 2-(N,C)-pyridine ] and benzene. Each tantalum atom is bound unsymmetrically to one C=C bond of benzene with a weak interaction to a third carbon atom the bonding may be described as a distorted tj3-enyl. In the dinuclear cobalt complex XII, the xylene functions as a bis(enyl)-ligand (12,22). [Pg.189]


See other pages where Cobalt naphthalene is mentioned: [Pg.548]    [Pg.135]    [Pg.548]    [Pg.135]    [Pg.421]    [Pg.236]    [Pg.173]    [Pg.280]    [Pg.458]    [Pg.327]    [Pg.82]    [Pg.153]    [Pg.273]    [Pg.38]    [Pg.663]    [Pg.471]    [Pg.58]    [Pg.67]    [Pg.201]    [Pg.394]    [Pg.13]    [Pg.379]    [Pg.162]    [Pg.1245]    [Pg.58]    [Pg.67]   
See also in sourсe #XX -- [ Pg.4 ]

See also in sourсe #XX -- [ Pg.429 ]




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