Urea-formaldehyde resins applications

Application Urea-formaldehyde resins are used as adhesives in the wood-working industry and are typically used in the production of plywood and particle board. They are available as concentrated solutions or in powder form as a result of the spray-drying process. 

By far the preponderance of the 3400 kt of current worldwide phenolic resin production is in the form of phenol-formaldehyde (PF) reaction products. Phenol and formaldehyde are currently two of the most available monomers on earth. About 6000 kt of phenol and 10,000 kt of formaldehyde (100% basis) were produced in 1998 [55,56]. The organic raw materials for synthesis of phenol and formaldehyde are cumene (derived from benzene and propylene) and methanol, respectively. These materials are, in turn, obtained from petroleum and natural gas at relatively low cost ([57], pp. 10-26 [58], pp. 1-30). Cost is one of the most important advantages of phenolics in most applications. It is critical to the acceptance of phenolics for wood panel manufacture. With the exception of urea-formaldehyde resins, PF resins are the lowest cost thermosetting resins available. In addition to its synthesis from low cost monomers, phenolic resin costs are often further reduced by extension with fillers such as clays, chalk, rags, wood flours, nutshell flours, grain flours, starches, lignins, tannins, and various other low eost materials. Often these fillers and extenders improve the performance of the phenolic for a particular use while reducing cost. 

There is an obligation to respect limits of residual monomer rates. For example, after application of urea-formaldehyde resin, the residual rate of formaldehyde is limited according to national regulations... 

Other applications for phenolics are switchgears, handles, and appliance parts, such as washing machine agitators (that s why they re usually black). Phenolics are widely used to bond plywood, particularly exterior and marine grades. Although urea-formaldehyde resins are cheaper for this purpose, they were not nearly as water-resistant and have been limited to interior grades. Abrasive wheels and brake linings also are bonded with phenolic adhesives. 

Urea-formaldehyde resins are generally prepared by condensation in aqueous basic medium. Depending on the intended application, a 50-100% excess of formaldehyde is used. All bases are suitable as catalysts provided they are partially soluble in water. The most commonly used catalysts are the alkali hydroxides. The pH value of the alkaline solution should not exceed 8-9, on account of the possible Cannizzaro reaction of formaldehyde. Since the alkalinity of the solution drops in the course of the reaction, it is necessary either to use a buffer solution or to keep the pH constant by repeated additions of aqueous alkali hydroxide. Under these conditions the reaction time is about 10-20 min at 50-60 C. The course of the condensation can be monitored by titration of the unused formaldehyde with sodium hydrogen sulfite or hydroxylamine hydrochloride. These determinations must, however, be carried out quickly and at as low temperature as possible (10-15 °C), otherwise elimination of formaldehyde from the hydroxymethyl compounds already formed can falsify the analysis. The isolation of the soluble condensation products is not possible without special precautions, on account of the facile back-reaction it can be done by pumping off the water in vacuum below 60 °C imder weakly alkaline conditions, or better by careful freeze-drying. However, the further condensation to crosslinked products is nearly always performed with the original aqueous solution. 

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... 

It is important to realize that a thermosetting polymer reacted to high (but not full) conversion contains a small fraction of free monomers if the monomers are volatile, their emissions may produce forbidden contamination levels, particularly for indoor applications. The decline in the use of urea-formaldehyde resins in agglomerated wood panels resulted from contamination problems associated with formaldehyde emission. 

Formaldehyde evolution, at the hot press and in applications where adequate ventilation is lacking, result in relatively high levels of free formaldehyde fumes with the urea-formaldehyde resins. 

Urea is used as a solid fertilizer, a liquid fertilizer and miscellaneous applications such as animal feed, urea, formaldehyde resins, melamine, and adhesives. Presently, the most popular nitrogen fertilizer is a urea-ammonium nitrate solution. Urea-formaldehyde resins have large use as a plywood adhesive. Melamine-formaldehyde resins are used as dinnerware and for extra-hard surfaces (Formica ). The melamine is synthesized by condensation of urea molecules. 

Urea-formaldehyde resins are used for applications in which the panel is not in contact with water. For applications with high level of humidity, the phenol-formaldehyde resins are required. In all cases, free formaldehyde constitutes a dangerous pollutant that is slowly released and can be particularly toxic in confined rooms. Recent research has been done to substitute this type of resin by natural binders, such as cross-linkable proteins (Silvestre et al., 2000 Yang et al., 2006). 

Most furfural is produced from corncobs and oat and rice hulls, primarily by the Quaker Oats Company. The product is used in the chemical industry as a solvent and in wood rosin refining. A large amount of furfural is treated further to give furfuryl alcohol. The furfuryl alcohol is added to urea-formaldehyde resins in applications for adhesives and foundry core binders. 

Most of the formaldehyde produced is consumed in the production of urea-formaldehyde resins and phenol-formaldehyde resins. These cross-linked polymer products are in turn used in adhesive and laminate applications. 

Before the advent of oxygenate ethers like MTBE, formaldehyde production was the largest single application of methanol, with at least 16 manufacturers and consuming over 30% of the methanol produced. Formaldehyde is used in the manufacture of urea-formaldehyde resins, phenol-formaldehyde resins, melamine-formaldehyde resins, acetal resins, acetylenic chemicals, etc. The reactions involved in formaldehyde synthesis are ... 

The total world production of urea is about 100 million tons per year. By far the largest part of it is used as a nitrogen fertilizer both in solid form and in solution this consumes approximately 87% of all urea production. It is also a livestock feed additive (5%) and a raw material for urea-formaldehyde resins (6%) and melamine (1%). Other applications (1%) include its use as deicing agent, raw material for fine chemicals (cyanuric acid, sulfamic acid), formation of crystalline clathrates, and so on. 

The main application fields of aldehyde scavengers are PET (more specifically wafer bottles made from PET), and polyacetals such as POM or polymers synthesized from formaldehyde such as urea-formaldehyde resins. 

A large number of commercially important condensation polymers are employed as homopolymers. These include those polymers that depend on crystallinity for their major applications, such as rylons and fiber-forming polyesters, and the bulk of such important thermosetting materials like phenolics and urea-formaldehyde resins. In many applications, condensation polymers are used as copolymers. For example, fast-setting phenolic adhesives are resorcinol-modified, while melamine has sometimes been incorporated into the urea-formaldehyde resin structure to enhance its stability. Copolyesters find application in a fairly broad spectrum of end uses. 

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