Polyurethane coloration

Furfuryl alcohol, reacted with formaldehyde in the presence of acetic acid, is selective in yielding 2,5-bis(hydroxymethyl) furan. This crystalline solid monomer has been used in preparing polyesters and polyurethanes. Color stability has been a limitation in certain instances. Hydrogenation of 2,5-bis(hydroxy-methyl) furan to 2,5-bis(hyroxymethyl) tetrahydrofuran provides a water-white, stable, liquid diol that shows promise as a polyurethane/polyester component. In this instance, exceptionally color-stable products are produced (43). 

Uses. Neopentyl glycol is used extensively as a chemical intermediate in the manufacture of polyester resins (see Alkyd resins), polyurethane polyols (see Urethane polymers), synthetic lubricants, polymeric plasticizers (qv), and other polymers. It imparts a combination of desirable properties to properly formulated esterification products, including low color, good weathering and chemical resistance, and improved thermal and hydrolytic stabiUty. 

Acrylic Resins. The first synthetic polymer denture material, used throughout much of the 20th century, was based on the discovery of vulcanised mbber in 1839. Other polymers explored for denture and other dental uses have included ceUuloid, phenolformaldehyde resins, and vinyl chloride copolymers. Polystyrene, polycarbonates, polyurethanes, and acryHc resins have also been used for dental polymers. Because of the unique combination of properties, eg, aesthetics and ease of fabrication, acryHc resins based on methyl methacrylate and its polymer and/or copolymers have received the most attention since their introduction in 1937. However, deficiencies include excessive polymerization shrinkage and poor abrasion resistance. Polymers used in dental appHcation should have minimal dimensional changes during and subsequent to polymerization exceUent chemical, physical, and color stabiHty processabiHty and biocompatibiHty and the abiHty to blend with contiguous tissues. 

Paints are complex formulations of polymeric binders with additives including anti-corrosion pigments, colors, plasticizers, ultraviolet absorbers, flame-retardant chemicals, etc. Almost all binders are organic materials such as resins based on epoxy, polyurethanes, alkyds, esters, chlorinated rubber and acrylics. The common inorganic binder is the silicate used in inorganic zinc silicate primer for steel. Specific formulations are available for application to aluminum and for galvanized steel substrates. 

Electron beam-curable acrylate-modified colored polyurethanes. (Goodyear Tire and Rubber Co., USA). Jpn. Kokai Tokkyo Koho (1984), 4 pp. CODEN JKXXAF JP 59066413 A 19840414 Showa. Patent written in Japanese. Application JP 83-165284 19830909. Priority US 82-419864 19820920. CAN 101 73632 AN 1984 473632 CAPLUS. 

Polyurethane (PUR) is one of the most versatile plastics, due to the wide variation of the starting materials and by the use of practically all processing methods known in the plastics sector. Basically, what has been said in relation to the plastics considered so far can be applied to coloring PUR. 

P.Y.62 is thermally stable up to 250°C. It has a considerable effect on the shrinkage of HDPE and other partially crystalline polymers. The pigment is an equally suitable colorant for polystyrene and polyurethane and lends color to polypropylene spin dyeing products with minimal application requirements. 

P.O.34 is rarely used in polyolefins. In such media, it only withstands exposure to 200°C, and its opaque colorations show insufficient lightfastness. P.O.34 tends to bloom, especially in extrusion products made of low molecular weight LDPE types. The pigment is, however, recommended for a variety of other media. These range from aromatic polyurethane foams to cast resins of unsaturated polyester, in which the pigment slightly delays the hardening process. 

P.R.164 was also found in cast resin composed of methacrylate and unsaturated polyester. The pigment does not affect the hardening process of such media, which may be carried out, for instance, by using peroxides. An important field of application was in the coloration of various polyurethanes, for which the pigment was also sold in the form of a pigment preparation. 

The plastics industry uses P.R.222 primarily in polyurethane. The pigment exhibits average tinctorial strength. 1/3 SD colorations in HDPE, for instance (1% TiOz), are formulated at 0.23% pigment concentration. 

P.R.208 is also used in polyacrylonitrile spin dyeing. It exhibits excellent textile fastness properties and shows good lightfastness. Full shades (3% pigment concentration) equal step 7 on the Blue Scale, while very light (0.1% pigment) red specimens match step 5. The list of applications includes secondary acetate spin dyeing and mass coloration of polyurethane foam and elastomers. P.R.208 is inert to peroxides. 

P.Y.110 lends color to polystyrene and styrene containing plastics. It is a suitable candidate for unsaturated polyester and other cast resins, as well as for polyurethane. P.Y.110 is used to an appreciable extent in polypropylene spin dyeing, it is very lightfast in this medium. It is utilized in polyacrylonitrile spin dyeing and sometimes also in polyamide. Its fastness properties, however, especially its lightfastness, do not meet special application conditions (Sec. 1.8.3.8). 

A key factor in the preparation of polyurethanes is the reactivity of the isocyanates. Aromatic diisocyanates are more reactive than aliphatic diisocyanates, and primary isocyanates react faster than secondary or tertiary isocyanates. The most important and commercially most readily accessible diisocyanates are aliphatic and colorless hexamethylene-1,6-diisocyanate (HDI), isophorone diisocyanate (IPDI),and aromatic, brownish colored diphenylmethane-4,4 -diiso-cyanate (MDI), 1,5-naphthalenediisocyanate, and a 4 1 mixture of 2,4- and 2,6-toluenediisocyanates (TDI). 

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