Ureas, polymeric

The reaction conditions can be varied so that only one of those monomers is formed. 1-Hydroxy-methylurea and l,3-bis(hydroxymethyl)urea condense in the presence of an acid catalyst to produce urea formaldehyde resins. A wide variety of resins can be obtained by careful selection of the pH, reaction temperature, reactant ratio, amino monomer, and degree of polymerization. If the reaction is carried far enough, an infusible polymer network is produced. 

Uses. Furfuryl alcohol is widely used as a monomer in manufacturing furfuryl alcohol resins, and as a reactive solvent in a variety of synthetic resins and appHcations. Resins derived from furfuryl alcohol are the most important appHcation for furfuryl alcohol in both utihty and volume. The final cross-linked products display outstanding chemical, thermal, and mechanical properties. They are also heat-stable and remarkably resistant to acids, alkaUes, and solvents. Many commercial resins of various compositions and properties have been prepared by polymerization of furfuryl alcohol and other co-reactants such as furfural, formaldehyde, glyoxal, resorcinol, phenoHc compounds and urea. In 1992, domestic furfuryl alcohol consumption was estimated at 47 million pounds (38). 

Partially polymerized resins of urea are used by the textile industry to impart permanent-press properties to fabrics (see also Textiles, finishing). 

THPC—Amide Process. The THPC—amide process is the first practical process based on THPC. It consists of a combination of THPC, TMM, and urea. In this process, there is the potential of polymer formation by THPC, melamine, and urea. There may also be some limited cross-linking between cellulose and the TMM system. The formulation also includes triethanolamine [102-71-6J, an acid scavenger, which slows polymerization at room temperature. Urea and triethanolamine react with the hydrochloric acid produced in the polymerization reaction, thus preventing acid damage to the fabric. This finish with suitable add-on passes the standard vertical flame test after repeated laundering (80). 

Another useful reaction is the reaction of water with isocyanate to generate CO2 and urea groups which modify the polymeric stmcture. This vigorous reaction is also a prime source of exothermic heat to drive equation 3 to completion. 

In recent years, synthetic polymeric pigments have been promoted as fillers for paper. Pigments that ate based on polystyrene [9003-53-6] latexes and on highly cross-linked urea—formaldehyde resins have been evaluated for this appHcation. These synthetic pigments are less dense than mineral fillers and could be used to produce lightweight grades of paper, but their use has been limited in the United States. 

Association Complexes. The unshared electron pairs of the ether oxygens, which give the polymer strong hydrogen bonding affinity, can also take part in association reactions with a variety of monomeric and polymeric electron acceptors (40,41). These include poly(acryhc acid), poly(methacryhc acid), copolymers of maleic and acryflc acids, tannic acid, naphthoHc and phenoHc compounds, as well as urea and thiourea (42—47). 

Continuous production of urea—formaldehyde resins has been described in many patents. In a typical example, urea and formaldehyde are combined and the solution pumped through a multistage unit. Temperature and pH are controlled at each stage to achieve the appropriate degree of polymerization. The product is then concentrated in a continuous evaporator to about 60—65% soflds (31). 

Ammonia is used in the fibers and plastic industry as the source of nitrogen for the production of caprolactam, the monomer for nylon 6. Oxidation of propylene with ammonia gives acrylonitrile (qv), used for the manufacture of acryHc fibers, resins, and elastomers. Hexamethylenetetramine (HMTA), produced from ammonia and formaldehyde, is used in the manufacture of phenoHc thermosetting resins (see Phenolic resins). Toluene 2,4-cHisocyanate (TDI), employed in the production of polyurethane foam, indirectly consumes ammonia because nitric acid is a raw material in the TDI manufacturing process (see Amines Isocyanates). Urea, which is produced from ammonia, is used in the manufacture of urea—formaldehyde synthetic resins (see Amino resins). Melamine is produced by polymerization of dicyanodiamine and high pressure, high temperature pyrolysis of urea, both in the presence of ammonia (see Cyanamides). 

In the manufacture of highly resident flexible foams and thermoset RIM elastomers, graft or polymer polyols are used. Graft polyols are dispersions of free-radical-polymerized mixtures of acrylonitrile and styrene partially grafted to a polyol. Polymer polyols are available from BASF, Dow, and Union Carbide. In situ polyaddition reaction of isocyanates with amines in a polyol substrate produces PHD (polyhamstoff dispersion) polyols, which are marketed by Bayer (21). In addition, blending of polyether polyols with diethanolamine, followed by reaction with TDI, also affords a urethane/urea dispersion. The polymer or PHD-type polyols increase the load bearing properties and stiffness of flexible foams. Interreactive dispersion polyols are also used in RIM appHcations where elastomers of high modulus, low thermal coefficient of expansion, and improved paintabiUty are needed. 

Urea and poly(vinyl alcohol) form a polymeric carbamate ester (123—126) ... 

Thermosetting Reactive Polymers. Materials used as thermosetting polymers include reactive monomers such as urea—formaldehyde, phenoHcs, polyesters, epoxides, and vinyls, which form a polymerized material when mixed with a catalyst. The treated waste forms a sponge-like material which traps the soHd particles, but not the Hquid fraction the waste must usually be dried and placed in containers for disposal. Because the urea—formaldehyde catalysts are strongly acidic, urea-based materials are generally not suitable for metals that can leach in the untrapped Hquid fractions. Thermosetting processes have greater utiHty for radioactive materials and acid wastes. 

Scotts technology (17) uses fluid-bed (Wurster column) technology to apply polymeric coatings to a number of fertilizer substrates including urea, potassium nitrate, potassium sulfate, and monoammonium phosphate (MAP). The coating material is appHed as a water-borne latex onto the fluidized substrate. As the substrate is fluidized with warm air (40—50°C), water is driven off and the latex coalesces into a continuous film around the fertilizer particle. The particular latex compositions used have selected glass-transition and blocking temperatures, which enable quick removal of the water before the soluble fertilizer core dissolves. This obviates the need to use precoats prior to the latex appHcation. 

Handling and Storage. Cyanamide solution dimerizes to dicyandiamide and urea with the evolution of heat and a gradual increase in alkalinity accelerating the reaction. Storage above 30°C without pH stabilizer leads to excessive dimerization and can result in violent exothermic polymerization. Cyanamide should be stored under refrigeration and the pH tested periodically. Stabilized cyanamide can be kept at ambient temperature for a few weeks. 

Currently, there is continuing work on an iadustry standard method for the direct determination of monomer, dimer, and trimer acids. Urea adduction (of the methyl esters) has been suggested as a means of determining monomer ia distilled dimer (74). The method is tedious and the nonadductiag branched-chain monomer is recovered with the polymeric fraction. A micro sublimation procedure was developed as an improvement on urea adduction for estimation of the polymer fraction. Incomplete removal of monomer esters or loss of dimer duriag distillation can lead to error (75). 

Imidazolidin-2-one, 4,5-dihydroxy-4,4-di(p-bromophenyl)-reactions with urea, 5, 406 Imidazolidin-2-one, 1,3-divinyl-polymerization, 1, 280 I midazolidin-2-one, 1 -ethyl-3-vinyl-polymerization, 1, 279 Imidazolidin-2-one, 4-methylene-synthesis, 5, 140... 

Urea is sufficiently important as an additive to PF resins for OSB to warrant some discussion. It has had a large favorable economie impact on the OSB industry. When used, it is generally added after the polymerization is complete. Thus, it is not part of the polymer and does not have any direet effect on polymer resistance to hydrolysis, as might be expected if it was part of the polymer backbone. Under alkaline pH conditions, urea-formaldehyde adducts do not polymerize at a rate that is significant compared to the PF polymerization therefore, the urea does not participate signifieantly in the euring proeess of the PF, despite the faet that it is present during the cure. Since urea is not present in the cured PF polymer per se, it does not detract from the durability of the polymer. Despite this, it is possible to see redueed OSB durability as a result of formulated urea if its use has led to actual PF polymer application rates that are too low. 

Even though UF adducts are known to be present in OSB, formaldehyde emissions are not elevated over those expected of an unmodified PF. There are three reasons for this. First, the molar ratio of formaldehyde-to-urea in these situations is very low. It is at least an order of magnitude lower than practical molar ratios for curable UF resin binders. Second, UF adducts are quite stable under the alkaline conditions that prevail in PF-bonded OSB. Finally, the urea only reacts with the formaldehyde that was left behind during polymerization and would have been largely emitted in pressing and cool-down. Urea additions have been shown to reduce PF formaldehyde emissions from hot pressing [121 ]. 

Dunky, M., Urea-formaldehyde glue resins. In Salamone, J.C. (Ed.), Polymeric Materials Encyclopedia, Vol. 11. CRC Press, Boca Raton, FL, 1996. 

Urea has no promoting effect on the A AM polymerization initiated with Ce(lV) ion. Recently, Qiu et al. [24] have studied the effect of N-acryloyl-N -4-tolylurea (ATU), N-methacryloyl-N -4-tolylurea (MTU), and N-acetyl-N -4-tolylurea (AcTU) on A AM polymerization initiated with Ce(IV) ion and found that these three urea compounds have a high promoting effect on the polymerization of AAM. The data are cited in Table 4. 

Uses of Formaldehyde. Formaldehyde is the simplest and most reactive aldehyde. Condensation polymerization of formaldehyde with phenol, urea, or melamine produces phenol-formaldehyde, urea formaldehyde, and melamine formaldehyde resins, respectively. These are important glues used in producing particle hoard and plywood. 

This group includes many plastics produced by condensation polymerization. Among the important thermosets are the polyurethanes, epoxy resins, phenolic resins, and urea and melamine formaldehyde resins. 

A variety of methylols are possible due to the availability of six hydrogens in melamine. As with urea formaldehyde resins, polymerization occurs by a condensation reaction and the release of water. 

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