AU637042B2 - Removable pressure-sensitive adhesive compositions comprising acrylic based emulsion polymers - Google Patents

Description

OPI DATE 10/07/90 AOJP DATE 09/08/90 APPLN. ID 29110 89 PCT NUMBER PCT/US88/04558

PCT

INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (51) International Patent CiOssification 4 (11) International Publication Number: WO 90/06976 C09J 7/02, 7/04, C08L 33/06 Al (43) International Publication Date: 28 June 1990 (28.06.90) (21) International Application Number: PCT/US88/04558 (81) Designated States: AT (European patent), AU, BE (European patent), CH (European patent), DE (European pa- (22) Intemational Filing Date: 20 December 1988 (20.12.88) tent), FR (European patent), GB (European patent), IT (European patent), JP, LU (European patent), NL (Eu- Avc 1 c-t -rJ o c..RR.Po '~r1o Zi ropean patent), SE (European patent).

(71) Applicat: AVERY INTERNATIONAL CRPORA- FION [US/US]; 150 North Orange Grove Boulevard, Pasadena, CA 91103 Published With international search report.

(72) Inventors: BERNARD, Margaret 485 Juniper Street, La Verne, CA 91750 BERMAN, Stansliv 16318 Clymer Street, Granada Hills, CA 91344 (US).

(74) Agent: DILLARD, David. Christie. Parker Hale, 350 West Colorado Blvd., P.O. Box 7068. Pasadena, CA 91109-7068 63 7042 REMOVABLE PRESSURE-SENSITIVE ADHESIVE COMPOSITIONS COMPRISING ACRYLIC BASED EMULSION POLYMERS (57) Abstract A removable pressure sensitive adhesive composition comprises an acrylic-based emulsion polymer having a gel content of from about 70 to about 90 The polymer comprises about 90 to 99.5 parts alkyl acrylate monomers, up to about 2 parts polar monomers and up to about one part of a multifunctional acrylate monomer. The polymer is synthesized in the presence of a combination of anionic and non-ionic emulsifiers wherein the amount of anionic emulsifier exceeds the amount of non-ionic emulsifier. The composition preferably comprises one or more adhesion stabalizers, preferably a plasticizer in an amount of up to about 3 weight and a protective colloid in an amount of up to about 1 by weight.

PCT/US88/04558 SWO 90/06976 1 -1- REMOVABLE PRESSURE-SENSITIVE ADHESIVE COMPOSITIONS COMPRISING ACRYLIC BASED EMULSION POLYMERS FIELD OF THE INVENTION This invention relates to pressure-sensitive adhesive compositions and more particularly to removable pressure-sensitive adhesive compositions comprising acrylic-based emulsion polymers having a gel content of from about 70% to about BACKGROUND OF THE INVENTION Removable pressure-sensitive adhesives are used on a variety of products including labels, tapes and the like to enable the product to adhere to a substrate and then later be removed from the substrate without difficulty and without leaving a stain or residue. To be suitable for such applications, the pressuresensitive adhesive must have good adhesion with low peel strength and must not exhibit a significant increase in adhesion over time. Optimally, the pressure-sensitive adhesive should exhibit such physical properties on a S variety of substrates.

One commercially available removable pressuresensitive adhesive is an acrylic emulsion polymer which has poor mandrel performance and exhibits excessive adhesion buildup on some substrates over time. The WO 90/06976 PCT/US88/04558 -2- 1 product also performs only at a narrow coat weight range of 18 to 20g/m 2 and tends to be expensive.

Another commercially available removable pressuresensitive adhesive is a formulated rubber composition which, over time, tends to phase separate. This results' in edge ooze, face bleed and, on some substrates, excessive adhesion buildup. This formulation can only be coated at low speeds and the convertibility is poor.

One attempt to improve the performance of removable pressure-sensitive adhesives formed by acrylic emulsions involved the blending of two commercial polymers mixed with fillers and ionic crosslinkering agents. This formulation, however, suffered from incompatibility as shown by two different glass transition temperatures.

In addition, the adhesive left stains on certair substrates.

Accordingly, there is a need for a removable pressure sensitive adhesive which demonstrates good adhesion and removability properties over a long period of time and on a wide variety of substrates.

SUMMARY OF THE INVENTION The present invention provides a removable pressure-sensitive adhesive (PSA) composition which, when coated onto a support, labeJ stock such as high gloss paper and electronic data processing paper, provides low peel adhesion on a variety of substrates without significant adhesion buildup over time.

The PSA composition comprises acrylic-based emulsion polymers having a gel content of from about to about 90 percent and a swell ratio of from about to about 25. The polymers comprise from about 90 to about 99.5 parts of alkyl acrylate monomers having from 1 to about 12 and preferably from about 4 to about 8 W90/06976 PCT/US88/04558 WO 90/06976 -3- 1 carbon atoms in the alkyl chain. The polymers further compriseup to about two parts of a polar monomer such -oU c^ of >cs+ ve- O-,.rrN rlr as methacrylic acid, andkup to about one part of a multifunctional acrylate monomer.

The PSA composition preferably comprises one or more adhesion stabilizers including a protective colloid in an amount up to about 1 percent by weight of the monomers and a plasticizer in an amount of up to about 3 percent by weight of the monomers.

The polymer is preferably synthesized in the presence of a combination of anionic and non-ionic emulsifiers or surfactants which form part of the PSA composition. The total amount of anionic and non-ionic emulsifiers is not more than about 4.0 percent by weight of the monomers and preferably not more than about 3.7 percent by weight. The ratio of anionic emulsifier to non-ionic emulsifier is greater than one. The amount of anionic emulsifier is from about 1.5 to about 3 percent by weight of the monomer and the amount of non-ionic emulsifier is from about 0.5 to about 2 percent by weight of the monomers.

WO 90/06976 PCT/US88/04558 -4- 1 DETAILED DESCRIPTION In accordance with the present invention, there is provided a removable pressure-sensitive adhesive (PSA) composition comprising acrylic-based emulsion polymers.

The removable PSA composition, when coated onto facestock to form a label or the like, exhibits low peel adhesion, preferably on the order of about 50 to about 300 N/m on stainless steel, and does not experience significant increase in peel adhesion with time and/or temperature.

The acrylic-based emulsion polymers comprise from about 90 to about 99.5 parts, hta i t bL JhL, and preferably about 98 parts alkyl acrylate monomers.

;e3, Oe.e: r, Meuns pe.-c¢-rr- b t- Amounts less than about 90 parts alkyl acrylate in the polymer tends to lower the gel content and raise the glass-transition temperature resulting in poor removable properties. Polymers having more than about 99.5 parts alkyl acrylate tend to have insufficient cohesive strength and leave stains or residue when peeled away from certain substrates.

The alkyl acrylate monomers preferably have from 1 to about 12 carbon atoms in the alkyl chain and more preferably most of the alkyl acrylate monomer comprises from about 4 to about 8 carbon atoms in the alkyl chain.

S 25 The lower alkyl acrylates, i.e. those having 1 to 3 carbon atoms in the alkyl chain, are not preferred as they tend to affect adhesion properties of the PSA composition, impart too low of an adhesion, on at least some substrates. Homopolymers of alkyl acrylates having more than 12 carbon atoms in the alkyl chain, tend to be crystalline and are not preferred. However, noncrystalline copolymers including aklyl acrylates having more than 12 carbon atoms in the alkyl chain may be used as desired.

X 01

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WO 90/06976 PCT/US88/04558 Accordingly, polymers in which at least the majority of the alkyl acrylate monomers have from about 4 to about 8 carbon atoms in the alkyl chain are presently preferred as providing the optimum balance of hardness, adhesion and removability. Exemplary preferred alkyl acrylates suitable for use in the present invention include 2-ethylhexyl acrylate, butyl acrylate, heptyl acrylate, octyl acrylate, isooctyl acrylate and isobutyl acrylate. 2-ethylhexyl acrylate is presently preferred.

If the polymer contains less than about 97 or 98 parts alkyl acrylate monomers, it is preferred that the polymer further comprise up to about 10 parts of any other monomer such as vinyl acetate or the like.

In addition to the alkyl acrylate monomer, the acrylic-based emulsion polymers comprise up to about 2 parts of one or more polar monomers such as methacrylic acid, acrylic ac i, itaconic acid, maleic acid, or acrylamide. The polar monomers impart mechanical stability and cohesive strength of the polymer.

The polymers of the present invention further comprise up to about one part and preferably from about 0.1 part to about 0.3 part of at least one multifunctional acrylate monomer. Including the multifunctional acrylate monomers enables the desired gel contents of the polymer to be obtained. That is, without the multifunctional acrylate monomer, the gel content of the polymer tends to be too low. For most polymer formulations, the multifunctional acrylate monomer must be present in an amount of at least about 0.1 percent to obtain the desired gel content.

It has been found that the amount of multifunctional acrylate monomer should not exceed about one percent as such amounts tend to reduce the stability of the acrylic-based emulsion from which the polymers WO 90/06976 PCT/US88/04558 -6- 1 are prepared, resulting in coagulation of the emulsion particles during preparation. Amounts of the multifunctional acrylate monomer above about 0.3 percent are not preferred as no additional benefit, i.e. no additional increase in gel content is typically observed. Examples of suitable multifunctional acrylates include polyethylene glycol diacrylate, hexane diol diacrylate, ethoxylated trimethylpropane triacrylate, pentaerythritol triacrylate and polypropylene glycol diacrylate. Hexane diol diacrylate is presently preferred.

An initiator induces polymerization of the monomers. Any suitable initiator may be used.

Preferred initiators include peroxides and peroxydisulfates. The initiator is preferrably present in an amount of about 0.1 percent to about 0.2 percent of the monomer weights. The presently preferred initiators are potassium persulfate and the t-butyl hydroperoxide, particularly in combination with each other in a ratio of from about 1:1 to about 1:3. Such combinations are preferred as they tend to provide optimum control of the rate of initiation and of the percentage conversion, i.e. the amount of polymer formed at a given time.

The acrylic-based emulsion polymers of the present invention have a gel content of from about 70 to about percent by weight and preferably from about 75 to about 83 percent. As used herein, "gel content" refers to the percentage by weight of the polymer that is insoluble in tetrahydrofuran, toluene or other similar organic solvent.

It has been found that acrylic-based emulsion polymers having a ge-1 content of less than about percent tend to exhibit too much adhesion, particularly upon aging, and hence are not suitable for applications WO 90/06976 PCT/US88/04558 -7- 1 requiring a removable adhesive. Polymers having a gel content of more than about 90 percent tend to exhibit too little adhesion and hence are too removable for most applications.

Acrylic-based emulsion polymers having gel contents below about 75 percent and above about 83 percent are not preferred because such polymers tend to exhibit too much or too little adhesion respectively on certain substrates. Acrylic-based emulsion polymers having a gel content of from about 75 to about 83 percent are presently preferred as they tend to exhibit the desired amount of adhesion and removability on most substrates, including polar, non-polar and porous substrates.

Exemplary substrates include polyethylene, polypropylene, fiberglass, appliance enamel, glass, formica, manila tags and recycled corrugated cardboard.

The acrylic-based emulsion polymers further comprise a swell ratio of from about 15 to about 25 and preferably from about 18 to about 23. s used herein, "swell ratio" refers to the amount of organic solvent, specifically tetrahydrofuran, which a polymer can absorb without dissolving. For example, a swell ratio of indicates that one gram of polymer can absorb 15 grams of solvent without dissolving.

The swell ratio provides an indirect evaluation of the cross-linking density of the polymers. A swell ratio above about 25 is not preferred because it tends to indicate insufficient crosslinking which results in the polymer having too much adhesion on at least some substrates. A swell ratio below about 15 is also not preferred as it tends to indicate too much crosslinking which typically results in too little adhesion on at least some substrates.

PCT/US88/04558 WO 90/06976 -8- 1 While not critical, it is preferred that the glasstransition temperature (Tg) of the polymers be in the range from about -30'C to about -60'C and preferably from about -50'C to about -55C. It has been found that PSA compositions having a Tg from about -30'C to about and particularly from about -50'C to about exhibit the desired amount of tack, i.e. initial adhesion.

The soluble portion weight average molecular weight of the polymers is also not critical, but is preferably at least about 200,000. It has been found that polymers having a soluble portion weight average molecular weight of less than about 200,000 tend to exhibit too much adhesion and insufficient cohesive strength, resulting in residues being left on a substrate after removal of the PSA composition.

In addition to the acrylic-based emulsion polymers, the removablt. PSA composition preferably comprises one or more adhesion stabilizers to minimize peel adhesion buildup over time and/or with elevated temperatures.

Preferred adhesion stabilizers include one or more plasticizers and one or more protective colloids.

The plasticizer may be present in an amount of up to about 3 percent by weight based on the total weight of the monomers and is preferably present in an amount from about 1 percent to about 3 percent by weight.

Amounts below about 1 percent by weight are not preferred as the PSA compositions tend to exhibit insufficient removability on certain substrates, e.g.

polypropylene and formica, particularly upon aging.

However, for certain substrates, e.g. glass, a plasticizer need not be present. It is preferred that the plasticizer not exceed about 3 percent because the polymers tends to exhibit a reduction in shear properties and the PSA composition tends to exhibit WO 90/06976 PCT/ S88/04558 -9insufficient adhesion on certain substrates, e.g. glass, and hence is too removable from those substrates.

Any suitable plasticizer may be used. Preferred plasticizers are monomeric plasticizers including diakyl esters of dibasic acids such as dioctyl phthalate and dioctyl azelate. The presently preferred plasticizer is dioctyl azelate.

A protective colloid, also known in the art as a steric stabilizer, is preferably present in the PSA composition in an amount of up to about 1 percent by weight of the monomers and preferably from about percent to about 1 percent by weight of the monomers.

Compositions having less than about 0.5 percent by weight of the protective colloid arie not preferred because such .compositions tend to exhibit too great of an adhesion buildup on some substrates. For certain substrates, e.g. glass, the protective colloid need not be "present in the composition. If present, it is preferred that the, amount not exceed about 1 percent by weight because such compositions tend to exhibit too little adhesion and hence are too removable for some substrates.

Any suitable protective colloid may be used. The presently preferred protective colloid is a high molecular weight polyvinyl alcohol composition sold by Air Products under the trade name Vinol 540. This product is approximately 87 to 89% hydrolyzed, i.e.

polyvinyl acetate which has undergone about 89% hydrolysis to form polyvinyl alcohol, and has, according to the manufacturer, a molecular weight of about 105,000 to about 110,000. Other suitable protective colloids are believed to include polyethylene oxide and hydroxy ,ethyl cellulose.

To obtain emulsion polymers having the above parameters, it has been, found that the particle size of WO 90/06976 PCT/US88/04558 1 :he acrylic-based emulsion from which the polymers are synthesized should not exceed' about 210 nm. Such a particle size tends to stabilize the emulsion without decreasing the gel. content of the polymerized product.

It has also been determined that the preparation of.

acrylic-based emulsion polymers having gel content of from about 70 to about 90 percent with the desired peel adhesion requires the monomers to be polymerized in the presence of a -combination of anionic and non-ionic emulsifiers or surfactants.

The synthesis of the polymers in the presence of an anionic emulsifier alone was found to yield polymers with high gel content without coagulation but also with undesirably high peel adhesion and hence resulted in polymers that were insufficiently removable for the desired applications. It was further determined that the addition of a non-ionic emulsifier in combination with an anionic emulsifier reduced the peel adhesion of the polymers to the desired levels. The presence of a non-ionic emulsifier, however, tended to increase the particle size of the emulsion.

Accordingly, to maintain the desired parameters, the total amount of anionic and non-ionic emulsifiers is preferably maintained below about 4.0 percent by weight and more preferably below about 3.7 percent by weight based on the weight of the monomers. Emulsions having more than about 3.7 percent by weight emulsifiers and particularly more than about 4.0 percent by weight emulsifiers tend to have a reduced stability, e.g.

undergo coagulation, and hence are not preferred.

The amount of anionic emulsifier should be from about 1.5 to about 3.0 percent by weight and preferably from about 1.8 to about 2.1 percent by weight based on the weight of the monomers. When less than about percent by weight anionic emulsifier is used, the WO 90/06976 PCT/US88/04558 -11- 1 emulsion tends to lose stability resulting in coagulation of the emulsion particles.

The amount of non-ionic emulsifiers should be in the range of from about 10.5 to about 2.0 percent by weight and preferably frbomabout 1.3 to about 1.7 percent by weight based on the weight of the monomer.

Again, when less than about 0.5 percent non-ionic emulsifier is used, the emulsion tends to lose stability.

It has also been found that the weight ratio of anionic emulsifier to non-ionic emulsifier should be greater- than 1. That is, the amount of anionic emulsifier should exceed the amount of non-ionic emulsifier. If the ratio is below 1, the gel content tends to be low and the particle size of the emulsion tends to be high. A weight ratio of anionic to nonionic emulsifier of 2.1 to 1.5 is presently preferred.

The presently preferred anionic emulsifier is sodium sulfonate of ethoxylated octyl phenol sold by Rohm Haas under the tradename Triton X-200. Such an emulsifier contains about 20 moles of ethylene oxide per mole of ethoxylated octyl phenol. Other suitable anionic emulrifiers include alkyl polyether sulfosuccinates, alkylaryl polyether sulfosuccinates, alkylpolyether sulfonates and alkyl aryl polyether sulfonates.

WO 90/06976 PCT/14"S88/04558 -12- 1 The presently preferred non-ionic emulsifier is ethoxylated nonyl phenol sold by Rohm Haas under the tradename Triton N-11L. This emulsifier contains about moles of ethylene oxide per mole of ethoxylated nonyl phenol. Other suitable non-ionic emulsifiers include alkyl aryl polyether alcohols.

In addition to the anionic and non-ionic emulsifiers, the gel content and particle size is preferably controlled by the inclusion of a small amount of electrolyte such as tetrasodium pyrophosphate, -ammonium phosphate di- or mono-basic or the like in the emulsion. Tetrasodium pyrophosphate is presently preferred. The amount of electrolyte is preferably from about 0.15 to about 0.3 percent by weight based on the weight of the monomers. Less than about 0.15 percent by weight is not preferred because the gel content of the polymers tends to be too low. Use of more than about 0.3 percent by weight electrolyte is not preferred because it adversely affects the stability of the emulsion and the particle size tends to be high.

In addition to the various components mentioned above, the PSA composition may contain small amounts of various, other fillers such as coloring agents, e.g., like carbon black, titanium dioxide, organic dyes and the like, and thickening agents.

A preferred method for preparing acrylic-based.

emulsion polymers of the present invention comprises first preparing a catalyst feed and a pre-emulsion feed.

The catalyst feed comprises water and catalyst. Any suitable catalyst may be utilized. Sodium formaldehyde sulfoxylate is presently preferred. The pre-emulsion comprises the alkyl acrylate monomers, polar monomers, multifunctional acrylate i/onomers, plasticizer initiator, anionic and non-ionic emulsifiers and water.

WO 90/06976 PCT/US88/04558 -13- 1 In the method, catalyst and pre-emulsion feeds are ,added simultaneously to a suitable reactor. The feed rates for the catalyst and pre-emulsion feeds are adjusted so that tie monomers and catalyst are added to the reactor over a period of from about 2 to about 4 hours. After about 20% to about 60%, and preferably about 40 percent of the pre-emulsion feed and catalyst feed have been added, the pH of the resulting emulsion is adjusted to about 6.3 to about 6.5 by the addition of sodium bicarbonate or the like. At this point, the protective colloid is mixed with the catalyst feed. The catalyst feed and the pre-emulsion feeds are again added simultaneously to the reactor at the desired rates preferably over a period of about 1 to about 2 hours whereby the feeds end simultaneously.

It is not presently preferred to add the protective colloid to the monomers before polymerization begins because coagulation of the particles tends to occur. It is also not preferred to add the protective colloid after all polymerization has occurred because the protective colloid tends to be non-uniformly disbursed or distributed throughout the polymer which results in a reduced initial adhesion of the polymer and lower overall performance of the adhesive.

Polymerization results in the formation of a latex having a viscosity typically in the range of from about 2500 to about 3500 centipoise. If required for" the particular coating technique used, the viscosity can be increased by the addition of a thickener. A presently preferred thickener is ASE 60, a polyelectrolyte sold by Rohm Haas.

Once the viscosity has been adjusted to the desired level, if required, the latex can be applied to label facestock ;:or other backing material by conventional techniques such as die coating and roll coating.

WO 90/06976 PCT/US88/04558 -14- 1 Coating speeds of up to about 600 feet per minute can be used. Preferred coating thicknesses are from about to about 25 grams per square meter.

To enhance the anchorage of the PSA adhesive to the facestock, it is greferred to first apply a thin layer of primer coating, generally in the range of 1 to 6 grams per square meter onto the facestock. Commercially available permanent or semi-permanent pressure-sensitive adhesives or ethylene vinyl acetate polymer formulations having a peel adhesion of more than about 300N/m 2 are suitable as primers.

The 'SA compositions of the present invention provide stable long-term adhesion on a variety of substrates. Typical adhesions are on the order of about 50 to about 300 N/m on stainless steel. The compositions exhibit good temperature resistance, maintaining stability at temperatures of up to 100oC and preferably up to 130'C or more, good repositionability and good mandrel performance. Mandrel performance refers to the ability of the adhesive composition to adhere to a small diameter, 0.5 to 1.0 inches.

EXAMPLE 1 To a one liter, four necked jacketed reactor equipped with thermocouple, reflux condenser, stainless steel blade stirrer and nitrogen inlet tube, were charged 90 grams of deionised water, 1.2g of tetrasodium pyrophosphate (TSPP) and 0.1g of Aerosol MA-80, an anionic surfactant sold by American Cyanamid. A monomer mix consisting of 240g of 2-ethylhexyl acrylate, 152g of butyl acrylate, 8g of methacrylic acid, 8g of dioctyl azelate, O.8g of hexane diol diacrylate and 0.4g of t-.butyl hydroperoxide was added to 130g of water containing 30g of Triton X-200 and 6g of Triton N-lll and was agitated for sufficient time until the formation WO 90/069-8 PCT/ US8/04558 1 of a stable pre-emulsion feed. To the reactor charge was added 29g of the above pre-emulsion and the contents of the flask were agitated while purging nitrogen for 15-20 minutes and then heated to 40'C. At 40*C a solution of the initiator containing 0.2g of potassium persulfate, 0.03g of FeEDTA in 6g of water was added.

After about two minutes, 1.6g of a catalyst feed solution prepared by adding 0.4g of sodium formaldehyde sulfoxylate to 80g of water was added. After about 4 minutes when the peak exotherm was observed, the preemulsion feed and the catalyst B were added at rates of and 0.47g/min respectively. After 10 minutes the pre-emulsion feed rate was increased to 3g/min. A second catalyst feed solution was prepared by adding of a 10% solution of Vinol 540 to 40% of the first catalyst. After about 60% of the monomer feed was in, the second catalyst feed was added at a rate of lg/min.

Simultaneously, a solution of Ig of sodium bicarbonate (in 12g of water was added dropwise over a period of 15 minutes. The rate of agitation was increased from time to time to ensure proper mixing. When all the feeds were in, the temperature was raised to 60*C and maintained for 0.5 hr. The composition was then cooled and filtered through 100 mesh nylon sieve. The resulting composition had a solids content of 54%, a percent congulum of less than 0.01% and a viscosity of about 3600 centipoise as measured by a Brookfield viscometer.

EXAMPLE 2 Example No. 1 was repeated with the following changes. No polyvinyl alcohol, Vinol 540 was added in .the later part of the catalyst feed. The kettle charge had 120g of water and 1.2g of TSPP. The catalyst feed had 100g of water. The resulting WO 90/06976 PCT/US88/04558 -16- 1 composition had a solids content of 51.4%, less than 0.01% coagulum and a viscosity of 300 centipolse.

EXAMPLE 3 Example No. 1 was repeated with the exception that the monomer mix contained no dioctyl azelate and the kettle charge was the same as in Example 2. The resulting composition had a solids content of 51% less than 0.01% coagulum and a viscosity of 2700 centipoise.

EXAMPLE 4 Example 1 was repeated with the exception that no polyvinyl alcohol (Vinol 540) or dioctyl azelate was added.

EXAMPLE To the same setup as in Example 1 were added 90g of water, 1.2g of TSPP, 0.04g of FeEDTA and 0.4g of an anionic surfactant sold by American Cyanamid. A monomer pre-emulsion feed was made, by dissolving 30g of Triton X-200 in 150g of water and adding to it with agitation a slow stream of monomer mix consisting of 240g of 2-ethylhexyl acrylate, 152g of butyl acrylate, 8g of methacrylic acid, 0.8g of hexanediol diacrylate and 0.Sg of t-butyl hydroperoxide. After agitating for hr., 29g of the pre-emulsion feed was added to the reactor charge and was heated to 40'C. At this temperature, 2g of catalyst feed prepared by dissolving 0.64g of sodium formaldehyde sulfoxylate in 75g of water was added. When the temperature increased to 45*C the pre-emulsion and catalyst feeds were added over a period of 3 hrs. ensuring proper mixing. At the end of feeds, the temperature was raised to 60'C, maintained for hr. and cooled. The composition was filtered through SWO 90/06976 PCT/US88/04558 0 9 -17- 1 100 mesh nylon sieve. The composition had a solids content of 55%, and less than 0.01% coagulum.

EXAMPLE 6 Example 1 was repeated with 0.4g. of hexanediol diacrylate and with a constant feed rate of the preemulsion for three hours. The resulting composition had a solids constant of 54%.

EXAMPLE 7 Example 1 was repeated with 0.2g of t-butyl hydroperoxide, 1.0g of hexanediol diacrylate and 4g of methacrylic acid in the pre-emulsion feed. The catalyst feed had 0.2g of sodium formaldehyde sulfoxylate in total. The catalyst feed was added at a rate of 0.,67g/min. after the addition of 40% of the preemulsion feed.

EXAMPLE 8 The removability of the compositions of Examples 1- 7 were determining by measuring the 90' peel adhesion values initially and at regular intervals for a period of up to 2 weeks at ambient conditions and at one week at High gloss paper facestock was first coated with a primer of formulated Airflex 400 (an ethylene vinyl acetate polymer sold by Air Products) containing fillers to improve coatability and anchorage, to a coat weight of 1.5-3g/m 2 The compositions of Examples 1-7 were coated onto a silicone release liner to a coat weight of 15-25 g/m 2 and dried for 10 minutes at 70'C. The adhesive compositions were then transferred to the primed facestock. Standard sample sizes were cut and tested for 90' peel adhesion on appliance enamel according to PSTC )No. 2, Fifth Edition, utilizing a WO 90/06976PC/S8045 PCT/US88/04558 -18- 1 minute dwell.

in Table 1.

The results of the tests are shown below SAMPLE %GEL Ex. -1 79 Ex. 2 75 Ex. 3 78 Ex. 4 76 Ex. 5 83 Ex. 6 65 ci clean removal pt paper tare spt slight paper COAT WT. Z2-INITIAL 18 160 ci 17 190 Ci TABLE 1

ADHIESION

24 HIR.

180 c1 210 ci 160 C1 I WK. 50'c 200 cl 250 ci 280 cI 300 spt 325 spt 2 WK RM. TEMP.

140 CI 450 pt 256 spt 18-2 0 20-22 18-20 165 250 ci WO, 90/06976 PCT/1JS88/04558 1 EXAMPLE 9 The removability of the compositions of Examples 1 and 3 were determined on various substrates. The procedure followed was the same as set forth in Example 8. The results are shown in Table 2 below.

AIESIOI (t1,M 2

J

SA?IE FACE STC tv-- rmt- FIEIER- APPLTAW.2 RECIRIM LTnYIEN m~py1Dhe GtASS ENAMEL CORR)GAIM

(A~

C:

DC. 1 High Glos i'aper Ex. I HNigh Gow Paper EX. 1 High Gloss Paper D)c. 1 High Glos Paper De.1 IHigh G1666 Paper IEc.I EDP Dc. I ED Ex.I EDP IDC. 3 High Gloss Paper E~c. 3 High Gloss Paper ci clean riimwal Initial 123 ci I1wek 140 cl 4,wekS 140 ci 9 weks 105 ci .12 weeks 88cl 1L23 cl 105 ci 105 cl 53 ci GUM' ituffc~ PWUA

TAG

53 cl, 105 ci 70 cl 53 ci 140 ci 123 Cl 70 ci 140 ci 105 CI 140 ci 1L23 Cir 140 Ci 140 cl 223 CIL 123 cl 105 ci 123 CI 105 ci, 175cl 1L23 cl 140 CI Initial 1 Veek 4 w~eeks 8 weks 12 weelw initial 8s Ci 53 cl 53 CI 70 ci 53 CI Be Val 53 ,51 70 CIL 70 Ci 95 3fr, 70Ocl 5 lScl 123 CI 88 ci 175 cl 123 Cl 53 ci 105 cl 53 ci 70 cl Be ci so CI as CiL 70 CI 70 CI 8s CI 70 cl 140 cl 158 CI 140 ci 140 CIL 175 ci 123 cl.

Be Ci 123 -CI 105 CI 140 ci 130 CI 123 Cl 140 Ci 140 CI 140 CIL 15" ci m ~ci 53 Ci 53 CI 53 ci 105 CI 105 ci 100 CIL 140 CI 140 ci 140 cl 175 cl 157 C1 130 ci.

105 Ci 105 Ci 105 Ci 123 CI 123 CI V9i 95 CI 140 cl 70 CI.

as CI 53 ci 70 CI 123 ci 90 ci 110 ci 1week 67 cl at 195 ci 275 pt 105 cl 110 71 172 cl pt- paper tarm vsi very slight leginess sf0 sictit fiber 1!ick (picks up fibers of Mrdx~ard) WO 90/06976 PCT/ US88/04558 -22- 1 The above description has been presented with reference to preferred compositions and preparatory methods. Workers skilled in the art and technology to which this invention pertains will appreciate that alterations and changes in the described compositions and method can be 'practiced without meaningfully departing from the principles, spirit and scope of this invention.

Accordingly, the foregoing description should not be read as pertaining only to the precise compositions and procedures described, but rather should be read consistent with and as support for the following claims which are to have their fullest fair scope.

Claims (31)

1. A removable pressure-sensitive adhesive composition comprising: an acrylic-based emulsion polymer having a gel content of from a 70 percent to 4te"t 90 percent comprising: from -a 90 to a~o-99.5 parts of at least one alkyl acrylata monomer; c vc.,oc,+ up to £u.i-2 parts of at least one polar monomer; and ositve up to aut one part of at least one multifunctional acrylate monomer; an anionic emulsifier in an amount of from *ebet 1.5% to about-3.0% by weight based on the weight of the monomers; a nonionic emulsifier in an amount of from to-b 2.0% by weight based on the weight of the monomers; and wherein the total amount of the arionic a-d non-ionic emulsifiers is not more than -abeet- 4.0% by weight based on the weight of the monomers and wherein the weight ratio of anionic emulsifier to nonionic emulsifier is at least abkot one.

2. A removable pressure-sensitive adhesive composition as claimed in claim 1 further comprising at least one adhesion stabilizer.

3. A removable pressure-sensitive adhesive composition as claimed in claim 2 wherein the adhesion stabilizer is a plasticizer in an aeunt up to about 3% by weight based on the weight of the monomers. WO 90/06976 PCr/S8804558 S4. A removable pressure-sensitive adhesive composition as claimed in claim 2 wherein an adhesion stabilizer is a protective colloid in an amount up to -abpu 1% by weight based on the weight of the monor.ers. A removable pressure-sensitive adhesive composition as claimed in claim 1 further comprising at least one electrolyte in an amount of up to-4bout-0.3% by weight based on the weight of the monomers.

6. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein the acrylic based emulsion polymer has a gel content of from 4bou-t- to about 83 percent.

7. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein the acrylic- based, emulsion polymer has a swell ratio of from abo;-- to ab 4

8. A removable pressure-sensitive adhesive composition as claimed in claim 7 wherein the acrylic- based emulsion polymer has a swell ratio of from about 18 to abe- 23.

9. A removable pressure-sensitive adhesive, composition as claimed in claim 1 comprising a glass- transition temperature of from eabeut -3,0"C to abe-t -606C. A removable pressure-sensitive adhesive composition as claimed in claim 1 comprising a glass- transition temperature. of from -b 5 0 -50'C to -eo-- WO 90/06976 PcT/US88/04558 1 11. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein the anionic emulsifier is present in an amount of from abe#t 1.8% to aou- 2.1% by weight based on the weight of the monomers.

12. A removable pressure-sensi-ive adhesive composition as claimed in claim 1 wherein the nonionic emulsifier is present in an amount of from aebet 1.3% to -eboe- 1.7% by weight based on the weight of the monomers.

13. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein the total amount of the anionic and nonionic emulsifiers is not more than by weight based on the total weight of the monomers.

14. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein the acrylic based emulsion polymer comprises about 98 parts alkyl acrylate monomers. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein at least a majority of the alkyl acrylate monomers of the acrylic- based emulsion polymer have from a.Amwt 4 to bout 8 carbon atoms in the alkyl chain.

16. A removable pressure-sensitive adhesive composition as claimed in claim 1 comprising a peel adhesion-in the range of from eka:-t-50 to .ae4t 300 N/m 2 on stainless steel. WO 90/06976 PCT/US88/04558 -26- 1 17. A removable pressure-sensitive adhesive composition having a peel adhesion of from a&Beet 50 to be, t-300 N/m 2 on stainless steel comprising: an acrylic-based emulsion polymer having a molecular weight of at least 4abat- 200,000, a gel content of from abut 70 percent to about 90 percent, a swell ratio of from aieak 15 to -bet- 25 and a glass transition temperature of from aout -60'C to 0ea comprising: from -Ut 90 to abAut °9.5 parts of at least one alkyl acrylate monomer having from one to a ealt twelve carbon atoms in the alkyl chain; C,_pc+n*eoo loTt up to abou 2 parts of at least one polar monomer; and from -abhu 0.1 to about 0.3 parts of at least one multifunctional acrylate monomer; a plasticizer in an amount up to aheot 3% by weight based on the weight of the monomers; a protective colloid in an amount up to ae-out 1% by weight based on the weight of the monomers; an anionic emulsifier in an amount of ,from abou. 1.5% to -ai-t 3.0% by weight based on the weighti of the monomers; a nonionic emulsifier in an amount of from abh 0.5% to aboe 2.0% by weight based on the weight of the monomers; and wherein the total amount of the anionic and nonionic emulsifiers is not more than a~he- 4% by weight based on the weight of the monomers and wherein the weight ratio of anionic emulsifier to nonionic emulsifier is at least about one. WO 90/06976 PC/US8/04558 -27- 1 18. A ,removable pressure-sensitive adhesive composition as claimed in claim 17 further comprising at least one electrolyte in an amount of up to -hetu-0.3% by weight based on the weight of the monomers.

19. A removable pressure-sensitive adhesive composition as claimed in claim 17 wherein the acrylic based emulsion polymer has a gel content of from -aiot- to e.t 83 percent. A removable pressure-sensitive adhesive composition as claimed in claim 17 wherein the acrylic- based emulsion polymer has a swell ratio of from-ee 18 to et 23.

21. A removable pressure-sensitive adhesive composition as claimed in claim 17 comprising a glass- transition temperature of from atut -50*C to ab11

22. A removable pressure-sensitive adhesive composition as claimed in claim 17 wherein the anionic emulsifier is present in an amount of from ajawa 1.8% to ebet- 2.1% by weight based on the weight of the monomers.

23. A removable pressure-sensitiVei adhesive composition as claimed in claim 17 wherein the nonionic emulsifier is present in an amount of from abot 1.3% to 4ae-it 1.7% by weight based on the weight of the monomers. WO 90/06976 PCT/ S88/0558 -28- 1 24. A removable pressure-sensitive adhesive composition as claimed in claim 1 wherein the total amount of the anionic and nonionic emulsifiers is not more than abeei 3.7% by weight based on the total weight of the monomers. A removable pressure-sensitive adhesive composition as claimed in claim 17 wherein the acrylic based emulsion polymer comprises about 98 parts alkyl acrylate monomers.

26. A removable pressure-sensitive adhesive composition as claimed in claim 17 wherein at least a majority of the alkyl acrylate monomers of the acrylic- based emulsion polymer have from ebet 4 to abt 8 carbon atoms in the alkyl chain.

27. An acrylic-based emulsion polymer having a gel content of from aija- 70% to a~it 90%, said acrylic- based emulsion polymer comprising: a, from 90 to bt 99.5 parts of at least one alkyl acrylate monomer having from one to abawk twelve carbon atoms in the alkyl chain; b. jup to .abeu 2 parts of at least one polar monomer; and c. Lup to abt one part of at least one multifunctional acrylate monomer.

28. An acrylic-based emulsion polymer as claimed in claim 27 having a gel content of from i4o 75% to abte 83%. WO 90/06976 PCT/US88/04558 -29- 1 29. An acrylic-based emulsion polymer as claimed in claim 27 comprising about 98 parts alkyl acrylate monomers.

30. An acrylate-based emulsion polymer as claimed in claim 27 wherein at least most of the alkyl acrylate monomers comprise from aheat- 4 to aet~- 8 carbon atoms in the alkyl chain.

31. An acrylic-based emulsion polymer as claimed in claim 27 comprising about 2 parts of a polar monomer.

32., An acrylic-based emulsion polymer as claimed in claim 27 comprising from bett 0.1 to abeet-0.3 parts multifunsional acrylate monomer.

33. An acrylic-based emulsion polymer as claimed in claim 27 comprising a swell ratio of from eabet' 15 to -abeo-

34. An acrylic-based emulsion polymer as claimed in claim 33 comprising a swell ratio of from a~tk t 18 to ctb 23.

35. An acrylic-based emulsion polymer as claimed in claim 27 comprising a glass-transition temperature of from aeot -30"C to ~bet

36. An acrylic-based emulsion polymer as claimed in claim 35 comprising a glass-transition temperature of from -4Ut -50C to bet- w 1 WO 90/06976 PC'i/US88/04558 1 37. A removable pressureP sensitive adhesive construction comprising: a face stock; a primer coating comprising an adhesive having a peel adhesion of at least abqeW 300 N/m 2 on stainless steel; and a removable adhesive coating over the primer coating comprising a removable pressure-sensitive adhesive composition comprising: an acrylic-based emulsion polymer having a gel content of from a"P-'t 70 percent to percent comprising: from abut 90 to a 99.5 parts of at least one alkyl acrylate monomer having from one to e t.Q twelve carbon atoms in the alkyl chain; c c 1 o .W ,up to al4,- 2 parts of at least one polar monomer; and ai e. c-ooM up to aa one part of at least one multifunctional monomer; an anionic emulsifier in an amount of from e 1.5% to 3.0% by weight based on the weight of the monomers; a nonionic emulsifier in an amount of from a 0.5% to-a by weight based on the weight of the monomers; and wherein the total amount of the anionic and nonionic emulsifiers is not more than a 4% by weight based on the weight of the monomers and the weight ratio of anionic emulsifier to non-ionic emulsifier is at least about one.

38. A removable pressure sensitive adhesive construction as claimed. in claim 37 wherein the primer coating has a coating weight of ao-u1 to-eke 6 grams per square meter. WO 90/06976 PCT/US88/04558 -31- 1 39. A removable pressure sensitive adhesive construction as claimed in claim 37 wherein the removable adhesive coating has a coating weight of from -abot 15 to about 25 grams per square meter. A removable pressure sensitive adhesive construction as claimed in claim 37 wherein the primer coating comprises a permanent of semi-permanent pressure sensitive adhesive or an ethylene vinyl acetate pollner formulation.

41. A method for making a removable pressure sensitive adhesive composition comprising: preparing a catalyst feed comprising catalyst and water; preparing a pre-emulsion feed comprising: water; from abeutk 90 to aeeMt 99.5 parts of at least one alkyl acrylate monomer having from one to -abut twelve carbon atoms in the alkyl chain; jsi+;eonoA-up to -abq 2 parts of at least one polar monomer; ci. posi\)Q '.mi up to about one part of at least one multifunctional acrylate monomer; from abt 0.1 to abt 0.2 parts of an initiator; and an anionic emulsifier in an amount of from abeot 1.5% to -ao" 3.0% by weight based on the weight of the monomers; a nonionic emulsifier in an amount of from abeat 0.5% to about 2.0% by weight based on the weight of the monomers; and wherein the total amount of the anionic and nonionic emulsifiers in not more than about.- 4% by weight based on the weight of the monomer and the WO :90/06976 PCT/US88/04558 -32- weight ratio of anionic emulsifier to nonionic emulsifier is at least about one; simultaneously introducing the catalyst feed and the pre-emulsion feed into a reactor at predetermined rates to thereby form the acrylic-based emulsion polymer

42. A method as claimed in claim 41 wherein the pre-emulsion feed further compricas a plasticizer in an amount of up to a 4 3% by weight based upon the total weight of the monomers.

43. A method as claimed in claim 41 wherein the pre-emulsion feed further comprises an electrolyte in an amount of up to ab 0.3% by weight based upon the total weight of the monomers.

44. A method as claimed in claim 41 further comprising introducing a protective colloid into the catalyst feed in an amount of up to about-1% by weight based upon the total weight of the monomers after from -abt 20% to aut 60% of the catalyst and pre-emulsion feeds have been introduced into the reactor and then cotinuing to introduce the catalyst and pre-emulsion feids into the reaction chamber. INTERiNATIONAL SEARCH REPORT Agiolicallon No _2CT/US8 8/04558 L. CLASSIFICATION Of 5 JICT MAT+tft st,*etas classification syrnbols OD7;"i, indicall1) 3 Acccroong 10o1 lnifal'ofldl Ptesnt ClAae'ficstion (PC) of to both National Classification and IPC IPC C09J 7/02, 7/04 C08L 33/06 T1 -fO _q-'241560; 526/75,3,17(321,324 WI FIELDS SIARCHED Miniomum 0ocuniation Searched Classification Systemn Classification Symbeols U. S. 428/355,500 526/75,317,321,324 524/5 ocurnwntation Starched other than Minimum Oocumientallon tie the tlten that such Oocumeorts are Included in the Filds Soafehed' Wl. DOCUMIENTS CONSIOERES TO 8E 1111LSVANT I& Categor'y *I Citation of Oocumvent. l aith indication. where aofslt.of the relevant massages i' helevant to Claim me. Is X A, 3,922,464 (Silver et. NOVEMBER 1975. A U.S,11 A 3,971,766 (Ono et. 27 July

1976. A A~ 3, 988, 392 (ameda et-. al.) 26 OCTOBER 1976. A Al 3,992,485 (Kosugi et. al.) 16 NOVEMBER 1976. A A, .4,033,918 (Hauber) 5 JULY 1977. X A, 4,110,290 (Mori et. al.) 27-36 29 AUGUST 1978. See Column 3, Example 1, Column 4, 3,ines -1-20. X A, 4,456,734 (Lizhdner et. al.) 27-36 26 JUNE 1984.- Se e column 3, the Examples. A A, 4,599,265 (Esmay) 8 JULY 1986. *SPecia CRIOgW611 01 cited d11CUmenIA ts later document vublished alter the intemnational fnate discumienti dolln tme general late Of the an Rhich is not or Oriority date and not in conflict wih n euca l"A conviderad to be of pauuo nivc cited to understand the *nnClor theory unttell'in the (E alng dten bu ul"e n ratrteinentoa documen"t 61 Particular relevance: the clairmed love~to fl~ng del.cannot be censivered novel or cannot be ceneeere to -V documentm which ma throw iouble en fonoitv cisien(sP of 4nvolve an Inventive step wh6Cht li cited to eGAtabig the sUbllcahe date of another y" document of Oorbcula, reloeec the clalimed invention Cilaobeors other epecilal reaaen Joe esogfisidl anniaf be considered Ie invelves an invenitve en elent the 0dacumnt role"li to en odlesure. use, eishibition at documet to comb~noe with oe or mere other Such 44mu- othor means miont,. such coffnbinabenif "eno obweus to a version sbda Sdecument Pubisehed Wleir to Mhe lntemasional filing date, but in the art. late than the prinuy date cillimed 14,* decunmon Member of the "aMo Patent family IVd. CEIMPICAION 0alo of the Actual Com ldn of lte Intemahnalt Seach I Oats of M c Report 06 MARCH 1989- -6omasenal 5.aiching Author"t I Signllgotku'cud I ISA/USHERBERT J. LILLING Porm faCTflAJ2I 0Ieocndy mime)I 1 3561ig lfbaAi.Iia~woe N& p /US88/04558 FURrTIfR INFORMATION CONTIMU90 PRO011-THE SECONDS *1411 X 4,629,663 (Brown et. al) 27-36 Y 16 DECEMBER 1986. See Table B, Example 13 in particular. 1-26P37-44 'Y U.S. A, 4,645,711 (Winslow et. al) 1-44 24 FEBRUARY 1987. See Table I.. A, 4,716,194 (Walker et. al.) 27-36 29 DECEMBER 1987. See column 1, Y lines 60-67, column 2, lines 45-54, 1-26, 37-44 column 3, lines 37-45, column 4, lines 9-19,36-40,,Table X=V Ex. OSSEV~llNS 120' VQ OSIVATONSWHERE CERTAIN CLAIMS WERE FOUND UNSILARCNASLE Is This intenm01oal rA mom Mego #108 bo"Ibliho i mooed~ @of.0.1 doin onw Lends, IW (al torlb leftiag mavens- Clim. ovinbees it'~DOIly144*£j' n I~A ouu ob ~dIdb eAM~E.ea.p 2Q2 cWaM numbers. .becase "Ie ret, to "s ftho -w MPON W do Pat comoly wth to rsabod toquke. Monts to OWCA em t tt mef me.,mIgtdletqhl koweb 1114011 be oslng VA U. I P VtQ3 OaSglVAflONS WHEOM UMfT OF INVammoi Io LACIe i This Inraons! Soowdap Aemoe 11101 InII11d 1 kwpl "Wtet n1 thil k eMWO 00oe go ft""w: IO As A rotulmi oadlal sesas Ieee weeo pi I#y* OW11 f soged. Wei beornallod sooc 9040 ""mAM 111 00abMo climst of the Mlaomaeuul aeg~tae. theonrsessoma o-'W abnabed sgtio tinhch Isot sweh "M blowfel @Pd-cvrsol NW o-u "dinoe owbn ors 11101 1114W o1V b11 1h geoi C..aegomd. WIN boAbNOad 0orth frit10 So ewdo to tin* muo firsmesol in oft del..s; X is covete by dol muabevs: all s iactibldmcotuld h eschodwlth~ouleln imflg muese oe h htmadSe0dgA otyI bill. aymoo 0mw it~omt e. Re~aron Pretsst o] The adolfoma somh Iso, Were occomwahod by so"Cac3 5.0001 03 "Go piut accompamlod MW popwt hoo ofd&emal seaah less. Fin. fCtLh2 I pawg.ho" PAW It" 66