The Chemistry of Phenolic Resins: The Formation, Structure and Reactions of Phenolic Resins and Related Products |
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acidic conditions Adler aldehydes alkaline amines ammonia Applied Chem Arkiv Kemi Mineral Auwers benzaldehyde catalyst CH₂ CH2 CH2 CH₂OH CH2OH CH2OH CH2OH CH3 CH3 CH2OH CH3 CH3 CH3 CH3 OH Chem chroman compounds condensation reaction cure dehydration dialcohol diazonium compounds dibenzyl ether dihydroxydibenzyl ethers dihydroxydiphenylalkanes dihydroxydiphenylmethanes equation esters Euler formaldehyde formation formed Geol H. L. Bender heating hexa hexamethylenetetramine Hultzsch hydrogen hydroxybenzyl Kemi ketones Kunststoffe Lebach Mannich bases methylene bridge methylene derivatives methylol group mole mole of phenol moles of formaldehyde Monatsh N. J. L. Megson novolac resins obtained OH CH2OH OH CH3 OH OH One-Stage resins ortho oxidation p-cresol phenol alcohols phenol-aldehyde phenolic hydroxyl group phenolic resins prepared quinone methide ratio react reaction mixture reaction of phenol reactive resole resorcinol S. R. Finn saligenin sodium sodium sulfite substituents sulfuric acid temperature tion unsaturated Vanscheidt xanthene Ziegler Zigeuner Zinke он он он