Resols acid cure

Phenol-Resole (Alcohol-Based) IMT-1312MS, INT-12 Phenol-Resole (Acid Cured) INT-1848PN... 

The importance of the nature of the catalyst on the hardening reaction must also be stressed. Strong acids will sufficiently catalyse a resol to cure thin films at room temperature, but as the pH rises there will be a reduction in activity which passes through a minimum at about pH 7. Under alkaline conditions the rate of reaction is related to the type of catalyst and to its concentration. The effect of pH value on the gelling time of a casting resin (phenol-formaldehyde ratio 1 2.25) is shown in Figure 23.15. 

Acid Curing. Urea-formaldehyde resins and resol-phenol-formaldehyde resins can be acid-cured by wastes from the production of maleic anhydride [1902]. The waste from the production of maleic anhydride contains up to 50% maleic anhydride, in addition to phthalic anhydride, citraconic anhydride, benzoic acid, o-tolulic acid, and phthalide. The plugging solution is prepared by mixing a urea-formaldehyde resin with a phenol-formaldehyde resin, adding the waste from production of maleic anhydride, and mixing thoroughly. 

Equation (2.47) is quite similar to Eq. (2.44), which means that acidic curing of resols is possible and may be achieved at room temperature by a variety of strong organic and inorganic acids. 

Baekeland [8, 9] was granted a patent in 1909 describing his alkaline-catalyzed Bakelite resins ( resoles ) and also the acid-cured novolak product. He conceived the idea of using counterpressure during hot cure to prevent bubbles and foaming from heat and was able to produce strong cured resinous products. 

Acid-curing resoles can be processed by hand-lamination, spray-up lamination, winding, and by infusion-technology, as well as by processes familiar from fiber-composite polymer (FCP) technology. Acid-resistant machine components and molds have to be used, and the shorter open times compared to polyester resins have to be taken into consideration. Compression processing, which is suitable for novolacs and resoles, requires ventilation strokes — as in most processing methods with closed molds - to let the developing water vapor escape. 

Phenolic Resins. Phenohc resins (qv) are formed by the reaction of phenol [108-95-2] C H O, and formaldehyde [50-00-0] CH2O. If basic conditions and an excess of formaldehyde are used, the result is a resole phenohc resin, which will cure by itself Hberating water. If an acid catalyst and an excess of phenol are used, the result is a novolac phenohc resin, which is not self-curing. Novolac phenohc resins are typically formulated to contain a curing agent which is most often a material known as hexamethylenetetraamine [100-97-0] C H22N4. Phenohc resin adhesives are found in film or solution... 

Most phenohc foams are produced from resoles and acid catalyst suitable water-soluble acid catalysts are mineral acids (such as hydrochloric acid or sulfuric acid) and aromatic sulfonic acids (63). Phenohc foams can be produced from novolacs but with more difficulty than from resoles (59). Novolacs are thermoplastic and require a source of methylene group to permit cure. This is usually suppHed by hexamethylenetetramine (64). 

Alkaline Catalysts, Resoles. Resole-type phenoHc resins are produced with a molar ratio of formaldehyde to phenol of 1.2 1 to 3.0 1. For substituted phenols, the ratio is usually 1.2 1 to 1.8 1. Common alkaline catalysts are NaOH, Ca(OH)2, and Ba(OH)2. Whereas novolak resins and strong acid catalysis result in a limited number of stmctures and properties, resoles cover a much wider spectmm. Resoles may be soHds or Hquids, water-soluble or -insoluble, alkaline or neutral, slowly curing or highly reactive. In the first step, the phenolate anion is formed by delocali2ation of the negative charge to the ortho and para positions. 

In some resole appHcations, such as foam and foundry binders, a rapid cure of a Hquid resin is obtained at RT with strong acid. The reactions proceed in the same manner as those of novolak resin formation. Methylol groups react at ortho and para phenoHc hydrogen to give diphenyknethane units (41). 

Resoles are usually those phenolics made under alkaline conditions with an excess of aldehyde. The name denotes a phenol alcohol, which is the dominant species in most resoles. The most common catalyst is sodium hydroxide, though lithium, potassium, magnesium, calcium, strontium, and barium hydroxides or oxides are also frequently used. Amine catalysis is also common. Occasionally, a Lewis acid salt, such as zinc acetate or tin chloride will be used to achieve some special property. Due to inclusion of excess aldehyde, resoles are capable of curing without addition of methylene donors. Although cure accelerators are available, it is common to cure resoles by application of heat alone. 

The PVF is made by acidic reaction between poly(vinyl alcohol) (PVA) and formaldehyde. The poly(vinyl alcohol) is, in turn, made by hydrolysis of poly(vinyl acetate) or transesterification of poly(vinyl acetate). Thus, residual alcohol and ester functionality is usually present. Cure reportedly occurs through reaction of phenolic polymer hydroxyls with the residual hydroxyls of the PVA [199]. The ester residues are observed to reduce bond strength in PVF-based systems [199]. This does not necessarily extend to PVF-P adhesives. PVF is stable in strong alkali, so participation of the acetals in curing is probably unimportant in most situations involving resoles. PVF is physically compatible with many phenolic resins. 

Youngquist etal. (1988) found improvements in both resin distribution and IB values when suitable emulsifiers were used in conjunction with waterborne resins, but considered it unlikely that the improvement in performance could be justified on cost grounds. It was postulated that acetylated wood interfered with the polymerization of the resin, so that it was not fully cured. It has also been suggested that acetic acid, which may be released during board pressing, could accelerate resin curing of resol type resins. In a study to determine whether this was so, acetylation of wood was found to slightly reduce... 

Carbohydrate-phenolic-based resins have shown promise for partial replacement of phenol and formaldehyde in exterior plywood adhesives (7,2). Such resins are produced in a two-stage reaction sequence. First, the carbohydrate is reacted with phenol, and sometimes urea, under acid catalysis at elevated temperatures (up to 150 °C), to produce an acid-stage resin. The acid-stage resin is then made basic, formaldehyde added, and the reaction continued at lower temperatures to produce a resol-type resin. Adhesives formulated from these resins have curing speeds consistent with present-day plywood production needs in the western United States, veneers are typically dried to 0 to 7% moisture content and the adhesive cured by hot pressing the panels at approximately 140 to 150 °C and 1.2 MPa. 

Curing Catalysts. If resol is heated to a high temperature, it can be cured without catalyst but in order to make curing it at an ambient temperature (room temperature), an acidic catalyst must be used. Both organic acid and inorganic acid catalysts can be used. Inorganic acids used include hydrochloric acid, sulfuric acid, and phosphoric acid, whUe benzene sulfonic acid, toluene sulfonic acid, and phenol sulfonic acid, are organic acids used. 

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