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Melamine coating resins

There are a number of possible configurations for the substituents on melamine coating resins ... [Pg.1110]

Isobutanol is used as a chemical intermediate in the preparation of isobutyl esters, isobutyl amines, and in isobutylated urea or melamine-coating resins. Isobutanol is used as a solvent in coating formulations with or without the cosolvent n-butanol. Nitrocellulose lacquers use isobutanol as a latent solvent, while the alcohol is an active solvent in automotive and furniture finishes, lacquers thinners, and hot spray lacquers. [Pg.90]

Urea—formaldehyde resins are also used as mol ding compounds and as wet strength additives for paper products. Melamine—formaldehyde resins find use in decorative laminates, thermoset surface coatings, and mol ding compounds such as dinnerware. [Pg.497]

Catalysts. The alkanolamines continue to find use as blocked catalysts for textile resins, coatings resins, adhesives, etc. Of particular utifity in curing durable-press textiles is AMP-HCl. Other salts, such as those of the benzoin tosylate or A-toluenesulfonic acid, find utifity in melamine- or urea-based coatings (18) (see Amino resins and plastics). [Pg.19]

Melamine—Formaldehyde Resins. The most versatile textile-finishing resins are the melamine—formaldehyde resins. They provide wash-and-wear properties to ceUulosic fabrics, and enhance the wash durabiHty of flame-retardant finishes. Butylated melamine —formaldehyde resins of the type used in surface coatings may be used in textile printing-ink formulations. A typical textile melamine resin is the dimethyl ether of trimethylolmelamine [1852-22-8] which can be prepared as follows ... [Pg.330]

Some of the chemicals mentioned above and others, such as chlorinated mbber or paraffin, antimony trioxide, calcium carbonate, calcium borate, pentaerythrithol, alumina trihydrate, titanium dioxide, and urea—melamine—formaldehyde resin, may be used to formulate fire retardant coatings. Many of these coatings are formulated in such a way that the films intumesce (expand) when exposed to fire, thus insulating the wood surface from further thermal exposure. Fire retardant coatings are mostly used for existing constmction. [Pg.329]

The term aminoplastics has been coined to cover a range of resinous polymers produced by interaction of amines or amides with aldehydes. Of the various polymers of this type that have been produced there are two of current commercial importance in the field of plastics, the urea-formaldehyde and the melamine-formaldehyde resins. There has in the past also been some commercial interest in aniline-formaldehyde resins and in systems containing thiourea but today these are of little or no importance. Melamine-phenol-formaldehyde resins have also been introduced for use in moulding powders, and benzoguanamine-based resins are used for surface coating applications. [Pg.668]

At one time urea-formaldehyde was used extensively in the manufacture of plywood but the product is today less important than heretofore. For this purpose a resin (typically U-F molar ratio 1 1.8)-hardener mixture is coated on to wood veneers which are plied together and pressed at 95-110°C under pressure at 200-800 Ibf/in (1.38-5.52 MPa). U-F resin-bonded plywood is suitable for indoor application but is generally unsuitable for outdoor work where phenol-formaldehyde, resorcinol-fonnaldehyde or melamine modified resins are more suitable. [Pg.678]

Melamine (I,3,5-triamino-2,4,6-triazine) was first prepared by Liebig in 1835. For a hundred years the material remained no more than a laboratory curiosity until Henkel patented the production of resins by condensation with formaldehyde. Today large quantities of melamine-formaldehyde resins are used in the manufacture of moulding compositions, laminates, adhesives, surface coatings and other applications. Although in many respects superior in properties to the urea-based resins they are also significantly more expensive. [Pg.680]

The industrial production and application of reactive and non-reactive microgels in organic coatings such as binders or components of binders, e.g. together with, e.g. acrylic and/or melamine/formaldehyde resins, especially for automotive coatings, was reported in a number of publications between 1980 and... [Pg.220]

Other NAD microspheres are composed of styrene, MMA, hydroxyethyl acrylate, acrylic acid and acrylonitrile and are blended with acrylic copolymers and melamine/formaldehyde resins [341,342]. Particles of this polymer are used as rheology modifiers to prevent sagging in automotive coatings and for controlling the orientation of metal flake pigments. [Pg.220]

Isocyanate and melamine-formaldehyde resins are commonly used as crosslinkers in automotive coatings. [Pg.77]

Clear coatings containing oligoester diols 1, 2, and 3 crosslinked with a hexakis(methoxymethyl)melamine (HMMM) resin were prepared, baked and tested. [Pg.325]

Another use of urea is for resins, which are used in numerous applications including plastics, adhesives, moldings, laminates, plywood, particleboard, textiles, and coatings. Resins are organic liquid substances exuded from plants that harden on exposure to air. The term now includes numerous synthetically produced resins. Urea resins are thermosetting, which means they harden when heated, often with the aid of a catalyst. The polymerization of urea and formaldehyde produces urea-formaldehyde resins, which is the second most abundant use of urea. Urea is dehydrated to melamine, which, when combined with formaldehyde, produces melamine-formaldehyde resins (Figure 96.2). Melamine resins tend to be harder and more heat-resistant than urea-formaldehyde resins. Melamine received widespread attention as the primary pet food and animal feed contaminant causing numerous cat and dog deaths in early... [Pg.289]

At an optimum addition level of only 1.5 w t %, nano-size magnesium-aluminum LDHs have been shown to enhance char formation and fire-resisting properties in flame-retarding coatings, based on an intumescent formulation of ammonium polyphosphate, pentaerythritol, and melamine.89 The coating material comprised a mixture of acrylate resin, melamine formaldehyde resin, and silicone resin with titanium dioxide and solvent. It was reported that the nano-LDH could catalyze the esterification reaction between ammonium polyphosphate and pentaerythritol greatly increasing carbon content and char cross-link density. [Pg.180]

In certain cases the acidity Melamine Formaldehyde resins (MF resins) or alkaline Polyurethane (also known us PU) resin (PUR resin) and alkali hardener (epoxy resin) can corrode or even totally dissolve the metallic pigments. In case of bronze pigments a color shift is possible. For these applications special metallic pigments are recommended, which are protected by an organic or inorganic coatings [14]. [Pg.219]

BERSET 2604 Is a melamine based resin with very low free formaldehyde content. It Is a very effective crosslinker and Insolublllzer for starch, protein, P.V.A., and latex In non-plgmented or pigmented coatings. When BERSET 2604 Is added to the coating color, good wet pick resistance and wet rub improvements are noticeable directly off the machine. [Pg.99]

Fig. 2 The o-P.s lifetime in the cylindrical pore at room temperature as a function of pore radius. In the model curve AR - 0.19 nm is assumed. The experimental points represent the peak value of the lifetime tjp and average hydraulic radius R. The triangles denote silica gels, dots - Vycor glasses, squares - melamine formaldehyde resins, diamond - Vycor glass with dextrane coating... Fig. 2 The o-P.s lifetime in the cylindrical pore at room temperature as a function of pore radius. In the model curve AR - 0.19 nm is assumed. The experimental points represent the peak value of the lifetime tjp and average hydraulic radius R. The triangles denote silica gels, dots - Vycor glasses, squares - melamine formaldehyde resins, diamond - Vycor glass with dextrane coating...

See other pages where Melamine coating resins is mentioned: [Pg.935]    [Pg.945]    [Pg.232]    [Pg.935]    [Pg.945]    [Pg.232]    [Pg.10]    [Pg.41]    [Pg.324]    [Pg.328]    [Pg.331]    [Pg.333]    [Pg.322]    [Pg.336]    [Pg.337]    [Pg.337]    [Pg.341]    [Pg.347]    [Pg.354]    [Pg.265]    [Pg.17]    [Pg.151]    [Pg.205]    [Pg.77]    [Pg.78]    [Pg.66]    [Pg.281]    [Pg.236]    [Pg.125]    [Pg.76]    [Pg.58]    [Pg.3322]   


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