Polyvinyl acetate-modified phenolic resin composition

Abstract

Adhesive compositions comprising a mixture of polyvinyl acetate and an alcohol soluble resol phenolic resin and about 2 to 20 parts by weight of lower polyhydric alcohol per 100 parts by weight of the resin solids have enhanced binding strengths on curing even after a prolonged open assembly time.

Description

BACKGROUND OF THE INVENTION

This invention relates to a polyvinyl acetate-modified phenolic resin composition having improved adhesion.

Polyvinyl acetate-modified phenolic resin is a thermosetting resin obtained by admixing an alcohol-soluble phenolic resin of the resol type with a polyvinyl acetate resin, and is characterized by properties different from those of alcohol-soluble resol type phenolic resin and of the vinyl acetate resin. Alcohol soluble resol resins (typified by resol resins soluble in lower monohydric alcohols such as methanol) are more particularly described in D. F. Gould "Phenolic Resins" Reinhold Publishing Corporation 1959, Chapter 3, the pertinent disclosure of which is incorporated herein by reference. Mixtures of phenolic resins and polyvinyl acetate are disclosed by Gould op cit page 95, lines 26-29. More specifically the polyvinyl-acetate modified phenolic resin is an advantageous adhesive in that it can meet the higher adhesive durability standard required in the specification of Type I plywood of JAS (Japanese Agricultural Standards) which is difficult to achieve with vinyl acetate resins. It is also advantageous in that the applicators and related equipment used with the resin mixture are washable with water, which advantage is not realizable in the case of alcohol-soluble resol type phenolic resins.

Adhesive compositions are prepared from such resins by the addition, directly before use, of a strongly acidic hardener such as benzenesulfonic acid or para-toluenesulfonic acid (used in sufficient proportion in the adhesive composition to impart a pH of about 0.1 to about 1.0 to the adhesive composition) which is applied onto the adherend. The resin-containing adherends are pressed under a pressure of about 2-15 kg/cm.sup.2 for about 5-20 hours at 15.degree.-40.degree. C. to cure the resin, thereby completing the adhesion. However, in comparison with alcohol-soluble resol type phenolic resins or vinyl acetate resins, the polyvinyl acetate-modified phenolic resins generally have a serious drawback in showing a significant loss in bonding strength when the socalled open assembly time, or the period between the coating of adhesive composition on the adherend and curing of the resin is long i.e. about 10 minutes or longer. The necessity of limiting open assembly time in using conventional polyvinyl acetate-modified phenolic resin compositions inevitably necessitates rapid processing in wood working plants, and eventually leads to defective adhesion of the resin product, particularly at high ambient temperatures.

This phenomenon can be ascribed to an insufficient flow of the adhesive composition when compressed after a prolonged open assembly time, and an insufficient bonding strength resulting therefrom due to the faster hardening speed of such an adhesive composition in comparison with that of ordinary alcohol-soluble resol type phenolic resins or of vinyl acetate resins, as the adhesive composition of polyvinyl acetate-modified phenolic resin containing a hardener already starts hardening on the adherend at normally encountered temperatures above 15.degree. C., and as the vinyl acetate resin used as its modifier is originally provided with a relatively fast drying speed.

SUMMARY OF THE INVENTION

It is now found that a sufficiently high bonding strength can be obtained even after a prolonged open assembly time by the addition of a saturated aliphatic polyhydric alcohol of 2 to 6 carbon atoms and 2 to 6 alcoholic hydroxy groups per molecule in an amount of about 2 to about 20 parts by weight to 100 parts by weight of polyvinyl acetate-modified phenolic resin solid. This may be ascribed to a suitable flow being retained by the plasticizing effect of polyhydric alcohol even after the adhesive composition of polyvinyl acetate-modified phenolic resin coated on the adherend hardens when compressed as explained above.

DETAILED DESCRIPTION OF THE INVENTION

The amount of polyhydric alcohol is preferably within a range of about 2 to about 20 parts by weight with respect to 100 parts by weight of polyvinyl acetate-modified phenolic resin solid. An addition in excess of this range results in reduced bonding strength due to an excessive plasticizing effect.

Generally the mixture of polyvinyl acetate and resol-type phenolic resin contains a weight ratio of vinyl acetate polymer to phenolic resin of from about 9:1 to about 1:1.

Lower polyhydric aliphatic alcohols for use in the present invention are exemplified by ethylene glycol, propylene glycol, glycerine, diglycerine, sorbitol, etc. Mixtures of these and equivalent polyhydric alcohols can also be used. The present invention is further illustrated by the following examples, which shall not be construed as limiting the scope of this invention. In these examples parts percentages and proportions are by weight unless otherwise specified.

EXAMPLE 1

(1) addition to ethylene glycol to polyvinyl acetate-modified phenolic resin

Adhesive compositions were prepared by the addition, to 100 parts of a polyvinyl acetate-modified phenolic resin (a mixture of an aqueous emulsion of vinyl acetate homopolymer and methanolic resol-type phenol-formaldehyde resin having a resin solids content of 60%), of 0, 2, 6, 10, 14 and 18 parts of ethylene glycol and then 5 parts of hardener (50% aqueous benzenesulfonic acid solution).

(2) Adhesion of wood

Wood samples were bonded with the above-mentioned adhesive compositions under the following conditions. The compressive shear bonding strengths obtained are summarized in the following Table 1.

______________________________________Adherend white firMoisture content 10 - 20 %Coating amount 250 g/m.sup.2 (coated on one side)Open assembly time 20 minutes at 20.degree. CClosed assembly time 1 minute at 20.degree. CCompression Temperature 20.degree. C Pressure 8 kg/cm.sup.2 Time 20 hoursConditioning after 24 hours at 20.degree. Cremoval of pressure______________________________________ Table 1______________________________________Compressive shear bonding strength(according to JIS-K-6802-1973)______________________________________CompositionPolyvinyl acetate-modified phenolic resin 100 100 100 100 100 100(parts)Ethyelene glycol (parts) 0 2 6 10 14 18Hardener (parts) 5 5 5 5 5 5Amount of ethylene glycolwith respect to 100 partsof polyvinyl acetate- 0 3.3 10 17 23 30modified phenolic resinsolid (parts)Compressive shear bondingstrengthBonding strength innormal state (kg/cm.sup.2) 11.5 49.5 58.2 53.2 46.5 38.5Wood failure in normalstate (%) 0 61 71 85 58 25Bonding strength afterrepeated boiling peeled 18.3 21.5 23.2 17.3 15.6(kg/cm.sup.2)Wood failure afterrepeated boiling (%) peeled 29 60 70 25 18______________________________________ As shown in Table 1, the adhesive composition containing 3.3, 10 and 17 parts of ethylene glycol with respect to 100 parts of polyvinyl acetate-modified phenolic resin solid showed higher bonding strengths than in the other compositions.

EXAMPLE 2

(1) addition of sorbitol to polyvinyl acetate-modified phenolic resin

Adhesive compositions were prepared by the addition, to 100 parts of polyvinyl acetate-modified phenolic resin (resin solid content 60%), of 0, 4, 8, 12, 16 and 20 parts of 70% aqueous sorbitol solution, and then of 5 parts of hardener (50% aqueous paratoluenesulfonic acid solution).

(2) Adhesion of wood

The wood samples were bonded with the above-mentioned adhesive composition under the following conditions. The compressive shear bonding strengths of the bonded samples are summarized in the following Table 2.

______________________________________Adherend birchMoisture content 8 - 12 %Coating amount 250 g/m.sup.2 (coated on one side)Open assembly time 20 minutes at 25.degree. CClosed assembly time 1 minute at 25.degree. CCompression Temperature 25.degree. C Pressure 12 kg/cm.sup.2 Time 20 hoursConditioning afterremoval of pressure 24 hours at 25.degree. C______________________________________ Table 2______________________________________Compressive shear bonding strength(according to JIS-K-6802-1973)______________________________________CompositionPolyvinyl acetate-modified phenolic resin 100 100 100 100 100 100(parts)70% Aqueous sorbitolsolution (parts) 0 4 8 12 16 20Hardener (parts) 5 5 5 5 5 5Amount of sorbitolwith respect to 100parts of polyvinyl 0 4.7 9.3 14 18.7 23.3acetate-modifiedphenolic resinsolid (parts)Compressive shear bondingstrengthBonding strength innormal state (kg/cm.sup.2) 52.0 105 143 153 140 95.3Wood failure in normalstate (%) 0 22 40 38 28 11Bonding strength afterrepeated boiling (kg/cm.sup.2) peeled 18.2 48.5 52.3 31.6 12.3Wood failure afterrepeated boiling (%) peeled 11 35 37 15 3______________________________________ As shown in Table 2, the adhesive compositions containing 4.7, 9.3, 14 and 18.7 parts of sorbitol with respect to 100 parts of polyvinyl acetate-modified phenolic resin solid showed higher strengths than in the other compositions.

EXAMPLE 3

(1) Addition of glycerine to polyvinyl acetate-modified phenolic resin

Adhesive compositions were prepared by the addition, to 100 parts of polyvinyl acetate-modified phenolic resin (resin solid content 60%), of 0 and 6 parts of glycerine and then of 5 parts of hardener (50% aqueous paratoluenesulfonic acid solution).

(2) Adhesion of wood

Wood samples were bonded with the above-mentioned adhesive compositions under the following conditions. The compressive shear bonding strength of these bonded samples are summarized in the following Table 3.

______________________________________Adherend Japanese cypressMoisture content 10 - 12 %Coating amount 250 g/m.sup.2 (coated on one side)Open assembly time 5, 10, 20 or 40 minutes at 20.degree. CClosed assembly time 1 minute at 20.degree. CCompression Temperature 20.degree. C Pressure 10 kg/cm.sup.2 Time 20 hoursConditioning afterremoval of pressure 24 hours at 20.degree. C______________________________________ Table 3__________________________________________________________________________Compressive shear bonding strength(according to JIS-K-6802-1973)__________________________________________________________________________CompositionPolyvinyl acetate-modified phenolic resin 100 100(parts)Glycerine (parts) 0 6Hardener (parts) 5 5Amount of glycerine withrespect to 100 parts ofpolyvinyl acetate- 0 10modified phenolic resinsolid (parts) (Without (With Polyhydric Alcohol) Polyhydric Alcohol)__________________________________________________________________________Open assembly time (minute) 5 10 20 40 5 10 20 40__________________________________________________________________________Compressive shear bondingstrengthBonding strength innormal state (kg/cm.sup.2) 79.3 63.2 21.5 peeled 61.5 68.5 75.3 69.4Wood failure innormal state (%) 86 28 0 peeled 63 71 83 75Bonding strength afterrepeated boiling 38.5 28.9 peeled peeled 35.2 39.2 38.9 37.6(kg/cm.sup.2)Wood failure afterrepeated boiling 68 25 peeled peeled 58 67 70 65(%)__________________________________________________________________________ As shown in Table 3, the adhesive composition containing 10 parts of glycerine with respect to 100 parts of polyvinyl acetate-modified phenolic resin solid showed higher bonding strengths for an open assembly time of about 10 minutes or longer in comparison with the adhesive composition with no addition of glycerine.

Claims

1. In an aqueous polyvinyl acetate-modified thermosetting resol phenolic resin adhesive composition wherein the weight ratio of polyvinyl acetate to resol resin is about 9:1 to about 1:1, the improvement wherein the composition comprises about 2 to about 20 parts per 100 parts by weight of the polyvinyl acetate modified phenolic resin solids of a lower saturated aliphatic polyhydric alcohol having 2 to 6 alcoholic hydroxy groups per molecule.

2. The composition as claimed in claim 1 wherein the phenolic resin is a phenol-formaldehyde resin.

3. The composition as claimed in claim 2 having a pH of about 0.1 to about 1.

4. The composition as claimed in claim 3 wherein the lower saturated polyhydric alcohol is selected from the group consisting of ethylene glycol, propylene glycol, glycerine, diglycerine, sorbitol and mixtures thereof.

5. The composition as claimed in claim 4 wherein the acid hardening agent is aqueous benzene sulfonic and the polyhydric alcohol is ethylene glycol.

6. The composition as claimed in claim 4 wherein the acid hardening agent is aqueous para-toluene sulfonic acid and the polyhydric alcohol is sorbitol.

7. The composition as claimed in claim 4 wherein the acid hardening agent is aqueous para-toluene sulfonic acid and the polyhydric alcohol is glycerine.