Melamine-form aldehyde

USA American Cyanamid Cymel 10776 9481 107 T Based on melamine-form-aldehyde resin and cellulose filler processable by moulding and injection moulding... 

Melamine-form aldehyde (MF) Stvrene-butadiene rubber (SBR)... 

Ibrahim NA (1992) New cation exchange composite based upon cellulose/melamine form-aldehyde/citric acid reaction products. J Appl Polym Sci 46 829-834... 

Group of plastics whose resins are formed by the condensation of melamine and aldehydes. 

Fig. 2.22 Temperature dependence of oxygen index for various plastics 1 rigid PVC, can not be measured above 105 due to softening 2 asbestos-filled phenol/form-aldehyde moulding compound 3 epoxy-modified melamine moulding compound 4 phenol/ formaldehyde moulding compound filled with wood flour 5 glass fibre-filled epoxy resin moulding...

A non-oxidizing alkyd contains non-drying (saturated) oils or fatty acids and therefore the alkyd is not capable of forming coherent film by air oxidation. Hence, the non-oxidizing alkyd is used as polymeric plasticizer or as hydroxyl-functional resin, which is cross-linked by melamine-formaldehyde or irrea-form-aldehyde resins or by isocyanatecross-linkers. The oil length for non-oxidizing alkyds is usually formulated below than 45% (Wicks et al., 1999). 

Resorcinol-formaldehyde resins are cold-setting adhesives for wood structures. Urea-formaldehyde adhesives, commonly modified with melamine formaldehyde, are used in the production of plywood and in wood veneering for interior applications. Phenol-form-aldehyde and resorcinol-formaldehyde adhesive systems have the best heat and weather resistance. 

A recent innovation in in-situ microencapsulation is the development of acid-triggered release of pesticide from the microcapsules [12]. Diols and aldehydes are reacted to form an acid labile acetal moiety. The acetal is then reacted with isocyanate to create a prepolymer. The prepolymer is a polyisocyanate cmitaining the acid labile moiety and suitable for in-situ shellwall polymerization. The prepolymer is dissolved into a pesticide, emulsified into water, and shellwall formed in-situ. Under alkaline or neutral pH conditions in a container, the insecticide is safely contained in the microcapsules. Acid could be added to the spray tank to rapidly release capsule contents prior to application. Alternate shellwall chemistry for in-situ microencapsulation utilizes etherified urea-formaldehyde prepolymers in the oil phase that are self-condensed with acid catalyst to produce encapsulating aminoplast shellwalls [13]. This process does not have the problem of continuing CO2 evolution. Water-soluble urea-formaldehyde and melamine-formaldehyde prepolymers can be selected to microencapsulate water or aqueous solutions [14]. 

The polyols for rigid foams (referred to as rigid polyols) discussed before (Chapters 13 and 14), are based on the alkoxylation of different polyols or polyamines, commercialised in a relatively high purity form. Some important starters for rigid polyols are obtained by the synthesis of the starter in situ, before the alkoxylation reaction, by the condensation reaction of some aromatic compounds (phenols, melamine and so on) with aldehydes (mainly formaldehyde), followed by the reaction of the resulting condensate with alkylene oxides. Some important rigid polyols based on the condensates mentioned are ... 

Aminoresins or aminoplastics cover a range of resinous polymers produced by reaction of amines or amides with aldehydes [14,46,47]. Two such polymers of commercial importance in the field of plastics are the urea-formaldehyde and melamine-formaldehyde resins. Formaldehyde reacts with the amino groups to form aminomethylol derivatives which undergo further condensation to form resinous products. In contras to phenolic resins, products derived from urea and melamine are colorless. 

Amino Rosins. Amino resins are the reaction product of an aldehyde with a compound containing an amino (—NH2) group (see Amino Resins). Both urea and melamine react with formaldehyde, first by addition to form methy-lol compounds, and then by condensation to form cross-linked polymers through methylene bridge and methylene ether formation. The cross-linking reactions are exothermic and produce water and formaldehyde as volatile products in reactions similar to resole phenolics, illustrated in equation 3. Urea-formaldehyde and melamine-formaldehyde account for the bulk of the amino resins. Their characteristics include water solubility and unlimited colorability with dyes and pigments. Applications include decorative high pressure phenolic laminates, adhesives in the laminated wood and furniture industries, and as an additive to textile fabrics to impart wash and wear properties. 

For the purposes of this chapter, aminopolymers are defined as polymers formed by the interaction of amines or amides with aldehydes. Of the various polymers of this type which have been investigated, only two are currently of appreciable commercial importance, namely urea-formaldehyde and melamine-formaldehyde polymers. In addition, melamine-phenol-formaldehyde and benzoguanamine-formaldehyde polymers find limited application. In the past there has been some commercial interest in thiourea-formaldehyde and aniline-formaldehyde polymers but these products are now of little importance. The aforementioned polymers form the contents of this chapter. 

Other thermosets besides phenol-aldehyde which are formed into network polymers by similar reactions are urea-aldehyde and melamine-aldehyde polymers. 

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