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Gaylord

Hydrides are available in many molecular sizes and possessing different reactivities. LiAIH reduces most unsaturated groups except alkenes and alkynes. NaBH is less reactive and reduces only aldehydes and ketones, but usually no carboxylic acids or esters (N.G. Gaylord, 1956 A. Haj6s, 1979). [Pg.96]

Gaylord, N. G, 1956, Reduction with Complex Metal Hydrides, Interscience New York... [Pg.368]

Acetal resins are typically suppHed in 25-kg multiwall bags and 500-kg Gaylords (rigid containers). Precompounded custom colors are available from manufacturers or the customer may use color concentrates. [Pg.60]

E. M. Fettes and F. O. Davis, in N. G. Gaylord, ed.. Polyethers, III, Polyalkylene Sulfides and Other Poly thioethers. Interscience PubHshers, New York,... [Pg.158]

Baked and Graphitized Products, Uses" under "Carbon" in ECT2nd ed., VoL 4, pp. 202—243, by W. M. Gaylord, Union Carbide Cotp. "AppHcations of Baked and Graphitized Carbon" under "Carbon (Carbon and Artificial Graphite)" in ECT 3rd ed., Vol. 4, pp. 596—622, by various authors. [Pg.523]

Gaylord and Miranda [Chem. Eng. Prog., 53, 139M (1957)] using a multitube cociirrent-flow faUing-film hydrochloric acid absorber for hydrogen chloride absorption found... [Pg.1402]

Numerous reports of comparable levels of success in correlating adhesion performance with the Scatchard-Hildebrand solubility parameters can be found in the literature [116,120-127], but failures of this approach have also been documented [128-132J. Particularly revealing are cases in which failure was attributed to the inability of the Scatchard-Hildebrand solubility parameter to adequately account for donor-acceptor (acid-base) interactions [130,132]. Useful reviews of the use of solubility parameters for choosing block copolymer compatibilizers have been prepared by Ohm [133] and by Gaylord [134]. General reviews of the use of solubility parameters in polymer science have been given by Barton [135], Van Krevelen [114], and Hansen [136]. [Pg.54]

Chevron Phillips Chemical Fleurchem Gaylord Chemical OxyChem... [Pg.57]

Gaylord Chemical Mallinckrodt Baker Merck (Germany)... [Pg.57]

Gayatri Minerals Chemicals, 171 Gaylord Chemical Corporation, 229 GE Petrochemicals, 229 GE Plastics, 229 GE Silicones, 229 GE Specialty Chemicals, 229 Gelest Inc., 229 GELVA , vinyl acetates, 71 GenCorp hic., 229... [Pg.333]

N. G. Gaylord, Reduction with Complex Metal Hydrides, Interscience, New York, 1956, KM6 pp. J. S. Pizey, Lithium Aluminium Hydride, Ellis Horwood, Ltd., Chichester, 1977,... [Pg.228]

See other pages where Gaylord is mentioned: [Pg.97]    [Pg.85]    [Pg.85]    [Pg.200]    [Pg.200]    [Pg.272]    [Pg.355]    [Pg.369]    [Pg.452]    [Pg.459]    [Pg.459]    [Pg.78]    [Pg.144]    [Pg.114]    [Pg.433]    [Pg.353]    [Pg.523]    [Pg.524]    [Pg.524]    [Pg.108]    [Pg.108]    [Pg.108]    [Pg.550]    [Pg.550]    [Pg.550]    [Pg.550]    [Pg.8]    [Pg.467]    [Pg.361]    [Pg.72]    [Pg.229]    [Pg.477]    [Pg.433]   
See also in sourсe #XX -- [ Pg.8 ]

See also in sourсe #XX -- [ Pg.217 ]

See also in sourсe #XX -- [ Pg.50 , Pg.107 ]



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