Chemical composition resorcinol-formaldehyde

However, lignin may find application as a suitable wood-composite adhesive in adhesive formulations if chemically modified in some manner. In this respect, the recent developments with soda bagasse lignin-resorcinol-formaldehyde and lignin-isocyanate adhesives allow for some cautious optimism for the future. 

The most common textile bonding compositions are, of course, the RFL (resorcinol-formaldehyde-latex) dips used to adhere tire carcass rubber to cord reinforcing members. A typical RFL composition calls for a latex terpolymer of styrene-butadiene-vinyl pyridine as well as the resorcinol and hexamethylene tetramine. Some natural rubber latex or regular SBR latex may also be added. The R F resin which forms in situ is able to react chemically with rayon by methylol etherification of the cellulose s hydroxyls. Similar reaction is likely with the amide groups of nylon fibers as shown in Figure 7. 

The phenolic family of adhesives are very diverse in their formulations and uses. Some are filled or modified with other polymers (vinyl, nitrile or epoxy). The composition depends largely on the intended use, e.g. for temperature and chemical resistance, or for water-proof wood bonding (phenol-resorcinol-formaldehyde). The majority are heat-curing although some wood-bonding adhesives can be cured at room temperature (RT). The comparison table includes Typical Use to differentiate between the types of adhesives. Phenolic adhesives are generally poorly represented by mechanical property data. 

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). 

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