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Urea-formaldehyde (UF), also known as urea-methanal, so named for its common synthesis pathway and overall structure, [1] is a nontransparent thermosetting resin or polymer. It is produced from urea and formaldehyde. These resins are used in adhesives, plywood, particle board, medium-density fibreboard (MDF), and molded objects.
Melting point: −92 °C (−134 °F; 181 K) ... Two steps in formation of urea-formaldehyde resin, which is widely used in the production of particle board.
The structure of the molecule of urea is O=C(−NH 2) 2.The urea molecule is planar when in a solid crystal because of sp 2 hybridization of the N orbitals. [8] [9] It is non-planar with C 2 symmetry when in the gas phase [10] or in aqueous solution, [9] with C–N–H and H–N–H bond angles that are intermediate between the trigonal planar angle of 120° and the tetrahedral angle of 109.5°.
Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9 Acetic acid: 1.04 117.9 3.14 16.6 ...
These included other types of cast phenolic resins similar to Catalin, and urea-formaldehyde resins, which could be made in brighter colors than polyoxybenzylmethyleneglycolanhydride. [4] [9] Once Baekeland's heat and pressure patents expired in 1927, Bakelite Corporation faced serious competition from other companies.
The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.
Biotin, a water-soluble B vitamin, is a bicyclic urea.. In chemistry, ureas are a class of organic compounds with the formula (R 2 N) 2 CO where R = H, alkyl, aryl, etc. Thus, in addition to describing the specific chemical compound urea ((H 2 N) 2 CO), urea is the name of a functional group that is found in many compounds and materials of both practical and theoretical interest.
To make polyoxymethylene copolymer, formaldehyde is generally converted to trioxane (specifically 1,3,5-trioxane, also known as trioxin). [18] This is done by acid catalysis (either sulfuric acid or acidic ion-exchange resins ) followed by purification of the trioxane by distillation and/or extraction to remove water and other active hydrogen ...