GB2073758A

GB2073758A - Pressure-sensitive adhesives

Info

Publication number: GB2073758A
Application number: GB8005185A
Authority: GB
Original assignee: Kendall Co
Current assignee: Kendall Co
Priority date: 1978-10-30
Filing date: 1980-02-15
Publication date: 1981-10-21
Also published as: AU531988B2; GB2073209B; FR2477172B1; NL186970B; CH644147A5; AT365219B; FR2477172A1; NL8001258A; BE881976A; AU5565180A; NL186970C; ATA105580A; BE537283A; DE3005381A1; NL80401C; GB2073209A; GB2073758B

Description

1 GB 2 073 758 A 1

SPECIFICATION Pressure-sensitive Adhesive

This invention relates to a composition useful as a pressure-sensitive adhesive which is a blend of a poly(vinyl lactam) and a copolymer of (1) an acrylic or methacrylic ester or a mixture of esters and (2) an ethylenically unsaturated acid, the blend possessing a unique combination of properties and 5 characteristics.

Pressure-sensitive adhesive compositions are commonly applied to the flexible backing or tape on which they are supported during use by coating them in the form of a solution or dispersion in a suitable vehicle such as an organic solvent or water or by coating them in the form of a hot melt free from vehicle. In order to be useful, pressure-sensitive adhesive compositions must possess not only 10 good tack but also good cohesive strength and the desired high degree of adhesion. All of these properties are generally interdependent, a change in one usually causing a change in the others. Although various low molecular weight homopolymers of alkyl acrylates have long been known to be tacky materials, they have possessed insufficient cohesive strength to be useful by themselves as pressure-sensitive adhesive, particularly those of the type used on tapes or backings intended to adhere to the skin, and it has been necessary to copolymerize them with selected other monomers to achieve the desired combination of properties, as described for example in Samour U.S. Patent 3,299,010.

It has also long been the practice to formulate pressure-sensitive adhesive compositions by blending together compatible components each of which in itself lacks one or more of the required properties but which combine to satisfy the requirements, as in the case of blends of two different hydrophobic water-insoluble copolymers as described in Guerin et al. U.S. Patent No. 4,045,517. It has also been proposed to react water-soluble poly(N-vinyl lactams) with polymeric carboxylic acids (including copolymers) to form water-insoluble compositions useful for a variety of purposes, as described in Stoner et al. U.S. Patent 2,901,457. As pointed out by Stoner et al. at column 4, lines 56-73, the reaction product there described always has substantially the same properties and contains the two polymeric components in the same proportions regardless of the proportions of the two used to make the product. The compositions of the present invention, on the other hand, vary in properties and in proportions of components depending upon proportions of starting materials. In Ono et al. U.S. Patent 3,975,570, it has been proposed to improve the moisture permeability of conventional pressure-sensitive adhe ives which are copolymers of alkyl acrylates with acrylic or methacrylic acid by blending with them hydroxyethyl cellulose, and it was stated that blends of such adhesives with poly(vinyl pyrroliclone) did not exhibit improved moisture permeability.

It has now been found that water-insoluble pressure-sensitive adhesive compositions having excellent tack, cohesion, and adhesion and capable of being applied to a backing by conventional hot melt coating equipment can be made by preparing an optically clear blend comprising a water-soluble poly(N-vinyl lactam) and a water-insoluble copolymer of (A) an ester or a mixture of esters having the structure R' 1 n2k'="-Co 1 U 1 K1 in which R' represents hydrogen or methyl and R, represents alkyl having 1 to 14 carbon atoms and (B) 40 from 1 to 12% preferably from 4 to 7% by weight of the copolymer of an ethylenic monomer containing an acid group, the copolymer being tacky, having a glass transition temperature below 01C, and having a viscosity of less than 50,000 cp at 350OF (1 76.7OC) and being soluble in organic solvents (i.e. substantially free from cross-linking), so that it possesses by itself insufficient cohesive strength to be useful as a pressure-sensitive adhesive.

The N-vinyl lactams, polymers of which can be used in the present invention include those having the structure IX, dr -c=o 1 'N 1 en=uji 2 in which X represents an alkylene bridge having three to five carbon atoms, such as 1 -vinyl-2 pyrrolidone, 1 -vinyl-5-methyl2-pyrrolidone, 1 -vinyl-2-piperidone, and N- vinyi-E-caprolactam; the 50 polymers may have molecular weights from 10,000 to 1,000,000 or more. Polymers of 1 -vinyl-2- 2 GB 2 073 758 A 2 pyrrolidone are preferred. The amount of polymeric N-vinyl lactam in the blend can vary from 1 to 30% by weight of the blend, depending upon the precise copolymer present and the precise properties desired in the blend.

The amount of copolymer present in the blend can be varied from 70 to 99% by weight of the blend. Preferably, the pressure-sensitive adhesive composition contains only the blend of polymeric N- 5 vinyl lactam and the specified copolymer, although small amounts of conventional additives such as stabilizing agents, may also be present to prevent deterioration of the blend during processing at elevated temperatures. Other conventional additives such as pigments, coloring agents and the like may also be present.

The ethylenic monomer containing an acid group which is copolymerizable with the ester can 10 contain a carboxylic acid group or sulfonic or phosphonic, such as acrylic or methacrylic acid, crotonic acid, maleic acid, 2-sulfoethyl methacrylate, and 1-phenyl vinyl phosphonic acid. Preferably the acid group in the ethylenic monomer is carboxylic, acrylic acid being the monomer of choice. The ester with which the ethylenically unsaturated monomeric acid is copolymerized may be for example butyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate and the c6rresponding methacrylates or mixtures thereof. 15 Esters of acrylic acid with mixtures of different alcohols having from 1 to 14 carbon atoms are preferred; particularly preferred are alkyl acrylates in which the alkyl groups have from 4 to 8 carbon atoms. The copolymer need not be one consisting solely of the specified ester monomer and ethylenic monomer containing an acid group but may contain up to 20%, by weight of the total copolymer, of another copolymerizable ethylenically unsaturated monomer such as vinyl acetate, styrene, or acrylonitrile. In general, the presence of such a third comonomer in the copolymer does not adversely affect the properties of the pressure-sensitive adhesive and may be desirable in some cases to reduce cost or to increase cohesive strength.

The blend can be made by mixing together solutions or dispersions of the polymeric N-vinyl lactam and of the copolymer in any desired vehicles or solvents which are miscible with each other, 25 then removing the vehicle or solvent, as by evaporation. It is also possible to blend the polymer or copolymer on conventional mixing equipment such as a two-roll mill or Sigma blade mixer.

In the case of those blends containing amounts of polymeric N-vinyl lactarrf near the upper end ot the specified range of proportions, i.e., from 10-30% by weight of the blend, the pressure-sensitive adhesive composition displays increased moisture vapor permeability as compared to compositions 30 containing smaller amounts of the polymer. This is an advantageous feature in the case of adhesive tapes or sheets having porous backing or reinforcement which are intended to be applied to the skin.

Although different polymers and copolymers are normally considered to be incompatible with one another when mixed, and incapable of forming a homogeneous blend having properties different from either of the components, the blends of the present invention are optically clear or at worst slightly 35 hazy in appearance, evidence that the blends are homogeneous at least to the extent that no discrete particles of either component greater than 4000 A in diameter are present. Because of this homogeneity, the low cohesive strength of the tacky copolymer is increased and the high fluidity is decreased by the presence in the blend of the polymeric N-vinyl lactam which acts as a reinforcing agent.

The blends of the present invention can be applied to any of the usual flexible backings or reinforcements employed in manufacturing adhesive tapes and sheets either by spreading, coating or casting a mixed solution or dispersion of the blend on the backing, then removing solvent or liquid vehicle, for example by evaporation; however, the blends possess the unique capability of being applied 46 in molten condition using conventional hot melt coating equipment because their hot melt viscosities are less than 100,000 cps at 3501F (1 76.70C); no curing or cross-linking of the blend is required.

Conventional pressure-sensitive adhesives containing copolymers of alkyl acrylates and acrylic or methacrylic acid of sufficiently high viscosity to have adequate cohesive strength, have a melt viscosity above 100,000 cps at 3501F (176.7 OC) and cannot be applied to a backing in molten condition using conventional equipment.

In order to achieve maximum stability and service life of the blend, it may be desirable to include in the pressure-sensitive adhesive composition, in addition to the polymeric N-vinyl lactam and the copolymer, a small amount of conventional stabilizer such as 1 % by weight of tetra kis-[2,4-di-tert butyl-phenyll-4,4'-biphenylylene-diphosphonite.

The following specific examples are intended to illustrate more fully the nature of the present 55 invention without acting as a limitation upon its scope. The molecular weights referred to herein are the peak molecular weights as determined by gel permeation chromatography.

A, Examples 1-15 A series of copolymers of alkyl acrylates with varying proportions of acrylic acid was prepared by conventional solution polymerization procedures by dissolving the desired proportions of monomers in 60 a suitable solvent such as benzene or ethyl acetate and by employing as the initiator of polymerization a small amount (0.1 % by weight of the monomers) of a free radical generator such as benzoyl peroxide or 2-t-butylazo-2-cyanopropane. Polymerization was carried out at 85-950C to a high degree of conversion, of the order of 97%, to provide copolymers having insufficient cohesive strength to be 3 GB 2 073 758 A 3 useful by themselves as pressure sensitive adhesives having molecular weights from 62,000 to 566,000. These copolymers after removal of the solvent by heating in vacuum were aggressively tacky in nature but lacked sufficient cohesive strength to be satisfactory pressure-sensitive adhesives by themselves. A tabulation of the copolymers and of their molecular weights follows:

Wt. Ratio of A crylic Acrylic Ester M04 Wt.

No Ester to A cid Thousands (1) n-Butyl 98:2 82 (2) 97:3 127 (3) 97:3 200 10 (4) 95:5 58 (5) 2-Ethyihexyl 98:2 566 (6) 2-Ethyihexyl 97:3 128 (7) 97:3 207 (8) 96.5:3.5 304 15 (9) 11 96:4 62 (10) 11 96:4 84 (11) 11 96:4 112 (12) 95.3A.7 105 (13) 94.5:5.5 85 20 (14) 94.5:5.5 105 (15) 93:7 105 A series of 1 -vinyl-2-pyrrolidone homopolymers all water-soluble but having different reported molecular weights, was obtained from commercial sources, as follows:

Polyvinyl Pyrrofidone 25 No. Mol. Wt., Thousands (1) 10 (2) 40 (3) 360 40 Blends of the foregoing two series in varying proportions by weight were then prepared as shown 30 in Table 1. In some cases, the acrylate copolymer, still in solution in the solvent in which it was polymerized, was mixed with a solution of the poly(vinyl pyrroliclone) in a compatible solvent such as chloroform and the two solvents were then removed by volatilization at reduced pressure. In other cases, the solvent was first removed from the solution of acrylate copolymer by heating at reduced pressure and the solvent-free copolymer was then blended with solvent free poly (vinyl pyrroliclone) by 35 milling on a heated 2-roll mill. The blend was then applied to a standard backing or support consisting of a 1. 5 mil polyethylene terephthalate film (Mylar (Registered Trade Mark)), the blends which were formed in solution being applied by speading the solution on the film before evaporating the solvent and the blends formed by milling being applied by calendering. The product in each case was a pressure-sensitive adhesive tape having an adhesive layer from 1-3 mils in thickness.

The adhesive properties of the tape were then determined with the results set forth in the following table. The probe tack was determined by means of a Polyken probe tack tester as described in U.S. Patent 3,214,971 having the following 4 functional parts: (1) a cylindrical steel probe attached to the compression loaded spring of (2) a series L Hunter mechanical force gauge (Hunter Spring Company, Brochure 750/FG, revised February 1961), (3) an annulus having an opening slightly larger than the diameter of the probe and (4)-a carrierfor the annulus which moves down to bring the annulus around the probe and then up to remove the annulus therefrom. The carrier moves at a speed of 0.1 inch (0.254 cm) per second. At the beginning of the test, the carrier is at its uppermost point of travel and the annulus rests upon the carrier so that the opening in the annulus is in line with the probe positioned beneath it. In carrying out the test, a strip of tape is placed upon the annulus, adhesive side 50 down, and spanning the annulus, opening. As the carrier is driven downwardly by the synchronous motor, the adhesive surface exposed through the opening is brought into contact with the flat surface of the probe so that the tape and the annulus attached thereto are suspended on the probe as the carrier continues farther on its downward path. The carrier then reverses its movement returning to pickup the annulus, thereby separating the tape from the probe surface. Separation begins after one 55 second contact between the probe and the adhesive. The force required to separate the tape from the probe is recorded on a gauge. The recorded value is the probe tack value. Measurements were made employing a loading of 100 grams/cm.l.

The peel adhesion values represent the.forces required to remove a oneinch wide adhesive tape from a stainless steel surface after contact therewith for 2 minutes at a temperature of about 751F 60 (23.90C). The tape is stripped from the surface at an angle of 1801 at a rate of 12 inches (30.5 cm.) per minute.

4 GB 2 073 758 A The creep resistance values are determined by providing a polished stainless steel tube, one inch in outside diameter, mounted horizontally within a constant temperature chamber maintained at 1 04'F+2F (40'C+ 1. 1 IC). The tube is provided with a slot 1/16 inch (0. 159 cm). wide extending along its upper face parallel to the tube axis. A six inch (15.24 cm.) length of adhesive tape to be tested is draped over the tube with its adhesive surface in contact with the tube and with its free ends 5 extending downwardly approximately the same distance on opposite sides of the tube, the tape extending across the slot perpendicularly thereto. Each length of tape is not over one-inch (2.54 cm.) wide and to each of its lower ends is secured a weight of one pound (454 grm.) per inch (2.54 cm) of tape width. After the weighted tape has been maintained in the chamber for 15 minutes, it is severed transversely along the gap in the slot and the time in hours required for downward movement of each 10 end by a distance of one half inch is measured. The creep resistance is expressed in hours.

The melt viscosity at 350IF (1 76.71C) is measured as Brookfield Thermosel (Viscometer Model

RVT) viscosity using a No. SC4-27 spindle at 2.5 rpm.

The results are as follows:

1 f r Table 1

Creep in hour A cryllc Poly(vinyl Wt. Ratio Viscosity at Probe Tack Adhesion to RoundBarat Copolymer No. pyrrolidone) No. Copolymer PVP 176.7 'C. cps x 10-3 at 100g1CM2 Steel ozlin. width 100 IF. 3 7. 8 'C, hours 1 3 90:10 <100 404 5.0 100+ 1 2 90:10 <100 930 48.0 0.3 3 2 87:13 <100 228 43.0 100+ 4 2 93:7 <100 336 44.5 1.1 4 2 90:10 <100 166 33.5 1.3 2 95:5 <100 398 40 10.0 1 90:10 <100 300 33 100+ 2 90:10 <100 262 31.5 100+ 3 90:10 <100 238 18.0 100+ 7 2 90:10 <100 140 - 100+ 7 2 85:15 <100 152 100+ 8 2 90:10 <100 308 - 100+ 8 2 85:15 <100 216 - 100+ 9 1 94:6 4 944 47 0.2 9 2 94:6 6.3 260 53 7.0 9 2 92:8 15.0 250 35 11.4 9 3 98:2 25.0 518 28 2.6 1 94:6 7.0 972 74 0.2 2 96:4 15.0 332 27 4.2 3 98:2 58.0 684 46 3.8 11 1 94:6 24.0 460 50 11.2 11 2 96:4 38.0 262 26 16.6 12 2 96:4 44.0 218 21 40.0 13 2 96:4 22.0 296 30 22.0 14 2 96:4 60.0 190 23 100+ 2 96:4 98.0 144 18 100+ Certain compositions of blends of alkyl acrylate copolymers containing higher proportions of PVP possess two times or greater water permeability (Table 11) than the conventional non-blended acrylate pressure sensitive'adhesives. Water permeability of an adhesive is a desirable characteristic especially in health care adhesive tape products for application to skin. It is measured by ASTM E96 Procedure E.

Table 11

Water Vapor Creep in hour Transmission Rate A crylic Poly(vinyl Wt. Ratio Probe Tack Adhesion to Round Bar at in gms of waterl Copolymer No. pyrrolidone) No. Copolymer.PVP at 100glCM2 steel ozlin. width 100'F. 37.8'C, hours 1 00IN2124 hrs 2 87:13 252 26.6 7.9 110 6 2 75:25 187 20.0 100+ 91.0 6 3 75.25 143 1 16.7 100+ 95.0 cn bi -j M CD G1 6 GB 2 073 758 A 6 The blend in each of the examples is an optically clear mixture, and, as can be seen from the foregoing, all of the blends form useful pressuresensitive adhesive tapes. It is also clear from the foregoing tabulation what effect is produced by variations in the dmount of acrylic acid present in the copolymer, the molecular weight of the copolymer, the relative proportion of copolymer to poly(vinyl pyrrolidone), and the molecular weight of the poly(vinyl pyrrolidone). The properties of other blends of the present invention can readily be determined by extrapolation or interpolation from the results set forth above, bearing in mind that in general lesser amounts of acid comonomers are required, when a sulfonic or phosphonic acid group is present, to achieve the same effect as when a carboxylic acid group is used.

Similar results can be obtained using copolymers of acrylic acid with other alkyl acrylates or 10 mixtures thereof and by using other water-soluble polyvinyl lactams in place of poly(vinyl pyrrolidone).

Claims

1. A composition comprising an optically clear blend of (1) a watersoluble polymer of a vinyl lactam having the structure dr FX-, -c= 0 1 'N / 1 CH=CH2 in which X represents an alkylene bridge having three to five carbon atoms, and (2) a tacky waterinsoluble copolymer comprising (A) an ester or a mixture of esters having the structure R' 1 1-12C=C-C=0 1 U 1 K1 in which R' represents hydrogen or methyl and R, represents alkyl having from 1 to 14 carbon atoms and (B) from 1 to 12% by weight, based on the copolymer (2) of an ethylenic monomer containing an 20 acid group, said polymer (1) being present in an amount from 1 to 30% by weight of the blend, said copolymer (2) being present in an amount from 70 to 99% by weight of the blend, having a glass transition temperature below 01C, and being substantially free from cross- linking with a viscosity of less than 50,000 cp at 350117 (1 76.7OC) so that it possesses by itself insufficient cohesive strength to be useful as a pressure-sensitive adhesive.

2. A composition as claimed in Claim 1 in which X represents -CH-CH 27CHi-.

3. A composition as claimed in Claim 1 or 2 in which R' represents hydrogen.

4. A composition as claimed in Claim 1, 2 or 3 in which R, represents alkyl having from 4 to 8 carbon atoms.

5. A composition as claimed in Claim 4 in which R, represents n-butyl.

6. A composition as claimed in Claim 4 in which R, represents 2ethylhexy].

7. A composition as claimed in any one of the preceding claims in which the monomer (B) contains a carboxyl group.

acrylic acid.

8. A composition as claimed in any one of the preceding claims in which said monomer (B) is

9. A composition as claimed in any one of Claims 2 to 8 inclusive in which the amount of polymer is from 1 to 8% by weight of the blend.

10. A composition according to Claim 1, substantially as hereinbefore described.

11. An adhesive sheet material comprising a flexible backing and supported thereon a pressure40 sensitive adhesive layer comprising a composition as claimed in any one of Claims 1 to 10.

12. The features as herein disclosed, or their equivalents, in any novel selection.

Printed for Her Majesty's Stationery Office by the Courier Press, Leamington Spa, 1981. Published by the Patent Office, 25 Southampton Buildings, London, WC2A 1 AY, from which copies may be obtained.

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