AU600278B2

AU600278B2 - Primed polyolefin surfaces for epoxy adhesives

Info

Publication number: AU600278B2
Application number: AU74120/87A
Authority: AU
Inventors: Frank John Armatis Jr.; James Joseph Kobe; John Thomas Simpson
Original assignee: Minnesota Mining and Manufacturing Co
Current assignee: 3M Co
Priority date: 1986-06-11
Filing date: 1987-06-11
Publication date: 1990-08-09
Anticipated expiration: 2007-06-11
Also published as: KR950010586B1; CA1326626C; JPS6311339A; AU7412087A; KR880000495A

Description

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i S S R 28870 FORM COMMONWEALTH OF AUSTRALIA PATENTS ACT 1952 COMPLETE SPECIFICATION

(ORIGINAL)

F,'R OFFICE USE: P i SIrn Class Int Class 0000 0 0 0D 0 0 Oo 0 0 c0 00 0- 00 000 an 0 0 We A 00

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00 0 Complete Specification Lodged: Accepted: Published: Priority: Related Art: Name and Address of Applicant: Minnesota Mining and Manufacturing Company 3M Centre Saint Paul Minnesota 55144 UNITED STATES OF AMERICA Address for Service: Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Complete Specification for the invention entitled: Primed polyolefin surfaces for epoxy adhesives The following statement is a full description of this invention, including the best method of performing it known to me/us 5845/3 '4 It It

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41676 AUS 2A -1- Descriptio PRIMED POLYOLEFIN SURFACES FOR EPOXY ADHESIVES Technical Field This invention relates to polyolefin substrates having a primed surface which provides improved bonding of epoxy resin adhesives thereto and a method for adhering primed polyolefin substrates with epoxy resin adhesives.

Background For many years there has existed a desire for 10 polyolefin materials which can be bonded to other materials, metals, ceramics and wood, or to themselves with epoxy resin adhesives. Bonding of such materials with epoxy resin adhesives is often desirable, particularly when the bonded material is to be subjected to conditions of high temperature and high humidity.

Untreated polyolefin substrates, e.g., polyethylene, polypropylene or polyallomer which is a copolymer of polyethylene and polypropylene, are generally unreceptive to epoxy adhesives and much effort has been expended in the search for a technique which will easily and reliably increase adhesion without significantly changing the properties of the substrate. Surface modification techniques for enhancing adhesive bonding which have been examined are treatment with helium gas plasma, oxygen gas plasma and chromic acid. These treatments and other surface modification procedures have a common shortcoming in poor durability. Light rubbing of the surface causes a decrease in the effect, the altered surface being easily abraded.

Irradiation of polyolefin substrates, such as with an electron beam, to improve the adhesion of various coatings is also known and has been disclosed in U.S.

Patents No. 4,041,192 (Heger et No. 4,148,839 (Fydelor), No. 3,252,880 (Magat et al.) and No. 4,179,401 (Garnett et al.).

Polyolefin substrates have been provided with a treated surface for improved adhesion of pressure-sensitive adhesives. Such pressure-sensitive adhiesives include rubber-type adhesives such as those based on natural rubber and synthetic rubbers, styrene-butadiene, chloroprene, neoprene, and isobutylene rubbers and synthetic resin-type adhesives such as acrylic, polyvinyl chloride, polyvinyl acetate, and polyvinyl butyral adhesives. U.S. Patent No.

3,628,987 (Nakata et al.) discloses a pressure-sensitive #cc adhesive film wherein the film surface to which the adhesive p s is adhered has graft-polymerized thereto a vinyl monomer or diene monomer, the adhesive having a solubility parameter ,c near that of polymers of the vinyl or diene monomer. U.S.

Patent No. 4,563,388 (Bonk et al.) discloses a polyolefin substrate having graft-polymerized thereto at least one monomer selected from the group consisting of acrylic acid, methacrylic acid and esters thereof; acrylamide; methacrylamide; sterically non-hindered tertiary alkyl acrylamides and methacrylamides having three or less carbo' ,atoms in the alkyl group; and N-vinyl pyrrolidone, and firmly adherently bonded to the graft-polymerized monomer an 25 acrylic type normally tacky and pre;.ure-sensitive adhesive.

A series of articles, "Surface Modification of Polyethylene by Radiation-Induced Grafting for Adhesive Boning. I. Relationship Between Adhesive Bond Strength and surface Composition," Yamakawa, J. Appl. Polym Sci, 3057-3072 (1976); "II. Relationship Between Adhesive Bond Strength and Surface Structure," Yamakawa et al., Macromolecules, 9, 754-758, (1976); "III. Oxidative Degradation and Stabilization of Grafted Layer," (S.

Yamakawa et al., J. Appln. Polym. Sci., 22, 2459-2470 (1978); "IV. Improvement in Wet Peel Strength," Yamakawa I -3et al., J. Appl. Polym. Sci., 25, 25-39 (1980), and "V.

Comparison with Other Surface Treatments," Yamakawa et al., J. Appl. Polym. Sci., 25, 40-49 (1980), disclose grafting of methyl acrylate (followed by saponification), vinyl acetate, acrylic acid, acrylamide, and methylolacrylamide to polyethylene by vapor-phase mutual grafting or liquid-phase preirradiation at thicknesses of grafted monomer of more than 10 micrometers to improve adhesion of epoxy adhesives.

Summary The present invention provides a polyolefin first substrate firmly adhered to a second substrate with an epoxy resin adhesive, said polyolefin first substrate having graft-polymerized thereto at least one monomer selected from the group consisting of sulfonic and carboxylic acids and alkyl esters thereof containing fewer than eight carbon atoms in the ester group, amides and mono- and di-substituted amides, alcohols, amines, epoxides, and and 7-membered heterocyclic rings having at least one oxygen and/or nitrogen atom in the ring, with the proviso that said monomer contain an ethylenically unsaturated polymerizable moiety, and that the graft-polymerized monomers are in a layer less than 5 micrometers in thickness and contacting said epoxy resin adhesive.

The present invention also provides a method for adhering a polyolefin first substrate to a second substrate with an epoxy resin adhesive comprising the steps of a) coating on said polyolefin first substrate a liquid monomer selected from the group consisting of sulfonic and carboxylic acids arid alkyl esters thereof containing fewer than e:Lght carbon atoms in the ester group, amides and mono- and di-substituted amides, alcohols, amines, epoxides, and and 7-membered heterocyclic rings having at least one oxygen and/or nitrogen atom in the ring, in a layer -4less than 5 micrometers in thickness with the proviso that said monomer contain an ethylenically unsaturated polymerizable moiety; b) irradiating the coated substrate with ionizing radiation to graft polymerize said monomer to said substrate; c) coating an epoxy resin adhesive on at least one of said graft-polymerized monomer surface of said I first substrate and (ii) a surface of said second substrate; d) contacting said surfaces and and i e) curing said epoxy resin adhesive.

Surprisingly excellent peel values, greater than 25 lb/in (440 N/dm), result when the grafted monomer layer is less than 5 micrometers thick. Good peel adhesion is also retained after exposure to water for a period of i about one week.

i Detailed Description SThe substrate of the invention is a polyolefin material, polyethylene, polyalkyl-a-olefins, and blends thereof, such as polyethylene, polypropylene, or polyallomer which is an ethylene/propylene copolymer.

These polyolefin materials can also contain small amounts, up to about 10 weight percent of modifying monomers, crosslinkable terpolymers, such as dicyclopentadiene and norborneene, and ionomers which enhance strength, such as acrylic acid. These terpolymers and ionomers are not present on the surface of the polyolefin materials in sufficient quantities to affect epoxy adhesive adhesion to Sthe polyolefin materials.

The thickness of the polyolefin material is Sdetermined by the end use of the adhesive-coated product, typical thicknesses being in the range of about 0.025 to about 5.0 millimeters. The polyolefin material may contain additives, such as carbon black, calcium carbonate, silica, titanium dioxide, crosslinking agents, dispersants and extrusion aids, which are known in the art.

Various specific monomers suitable for graft-polymerization onto polyolefin substrates to promote adherence of epoxy adhesives to the substrate include acrylic acid, dimethylacrylamide, diethylacrylamide, dipropylacrylamide, hydroxyethylacrylate, butanedioldiacrylate, hexanedioldiacrylate, diethylaminoethylacrylate, glycidylmethacrylate, isobutylmethacrylate, cyclohexylmethacrylate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, hydantoini hexacrylate, 2-vinyl-4,4-dimethylazlactone, and N-vinyl-pyrrolidone.

adtt 15 The monomer composition generally contains about o, 1 60 to about 100 weight percent monomer. The monomer composition applied to the polyolefin substrate may contain Otvarious additive such as crosslinking agents, surfactants, 0o0 alcohols, and acids.

S 20 Crosslinking agents, some of which may also be monomers suitable for grafting onto the substrate themselves, may be added to further enhance heat resistance

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of the product. Examples of useful crosslinking agents include polyethyleneglycol diacrylate, pentaerythritol tetraacrylate, tetraethylene glycol dimethacrylate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, allyl methacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, thiodiethylene glycol diacrylate, and triallyl cyanurate. The preferred obodot crosslinking agents include polyethylene glycol diacrylate, tetraethylene glycol dimethacrylate, trimethylol propane triacrylate, and thiodiethylene glycol diacrylate.

Crosslinking agents may.be present in monomer compositions in amounts of about 0 to about 80 percent by weight, preferably 0 to about 40 percent by weight.

-I -6- Surfactants may be present in the monomer composition to improve the uniformity of the coating on the substrate.

The thickness of the monomer composition is preferably less than about 5 micrometers, more preferably less than about 1 micrometer and most preferably less than about 0.5 micrometer.

For uniform application of the monomer to the polyolefin substrate, the substrate is preferably treated to enable a polar liquid to wet the surface. This can be achieved by treating the substrate with an oxidizing agent such as nitric acid or chromic acid, or treating the substrate with flame, plasma discharge or corona discharge.

The preferred method of treatment is corona discharge.

The monomer may be graft-polymerized to the substrate by use of actinic radiation such as x-rays, beta rays, gamma rays, ultraviolet light, visible light and electron beam irradiation. The preferred method of graft-polymerization is by irradiation with an electron beam. The electron beam dosage is typically greater than about 0.05 Mrads, preferaby greater than about 0.5 Mrads, and more preferably in the range of about 2 to about Mrads.

The substrate to which the polyolefin material is to be adhered can be any substrate which bonds well with epoxy adhesives. Such substrates include, for example, metals such as aluminum, steel, galvanized steel, stainless steel, copper, and titanium, plastics, otheL than polyolefins, such as polycarbonate, polyvinyl chloride, polyester and fiber-reinforced polyester, polymethylmethacrylate, and acrylonit :ile-butadiene-styrene, and particularly those plastics which are high-temperature impact modified, natural and synthetic rubbers, such as polychloroprene, styrene-butadiene rubber, and nitrile rubber, ceramics, wood, painted surfaces, glass primed with silane and polyolefin having a monomer graft-polymerized thereto according to the present invention.

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-7- Epoxy adhesives useful in the present invention include any one- or two-part epoxy adhesives as long as the curing temperature required does not exceed the softening temperature of the polyolefin substrate. In use the epoxy adhesive may be applied to either the polyolefin substrate or to the substrate to which the polyolefin material is to be adhered or to both substrates. Typical epoxy adhesives include Scotch-Weld brand Epoxy Adhesives 1838 and 2216 B/A, each available from Minnesota Mining and Manufacturing Company.

t The advantages of the invention are illustrated by the following examples, it being understood that numerous 15 variations will be well within the ability of those skilled in the art.

Example 1 Into a polyallomer resin, available from Tennessee 0 Eastman under the trade designation Tenite M 5321E, was milled 1% carbon black by weight. The composition was then extruded as a sheet having a thickness of about millimeter, after which one surface was corona-treated by passing the sheet through a 1 millimeter air gap between a chlorinated polyethylene-coated electrode and a grounded aluminum cylinder. The frequency of the unit was 16 kHz, the total input power being 1.5 kw and the exposure time of the sample being on the order of 0.6-1.0 sec. Over the corona-treated surface was then applied a blend of 80 parts by weight N,N-dimethyl acrylamide, 20 parts by weight trimethylol propane triacrylate, and 0.5 part by weight of a fluorochemical acrylate oligomer (a wetting and leveling agent commercially available from 3M Company as FC 4 3 0TM).

The blend, which had a viscosity of 2.3 cps at 25QC, was applied to the corona-treated polyallomer surface using a No. 200 quad knurled gravure roll in combination with a doctor blade, minimizing the coating thickness to less than one micrometer. The coated surface was then exposed to c_ -8electron beam irradiation at a dosage of about 4 Mrads and a voltage of 150-250 kv in a nitrogen atmosphere. The thickness of the grafted layer was found to be less than 0.4 micrometer using attenuated total reflection-infrared spectroscopy.

A cold-rolled steel panel x 12" x 0.32" (10 cm x 30 cm x 0.8 cm), designated 80-730F cold-rolled steel, B unpolished, 17603001, available from Advanced Coating Technologies, Inc., Hillsdale, Michigan) was wiped three times wi-ii methyl ethyl ketone to remove any surface oil present. Scotch-Weld® brand Epoxy Adhesive 1838-L B/A translucent was prepared by mixing together 6 parts by weight base and 5 parts by weight accelerator. The adhesive was coated on the steel panel and a one-inch wide x six-inch 15 long strip of polyallomer having the N,N-dimethyl 0 og acrylamide/trimethylolpropane triacrylate grafted thereto 0, was placed on the adhesive with the grafted surface a 0 contacting the adhesive and an end of the polyallomer 000 a extending beyond the plate. A 4,5 lb (2 kg) roller was b 20 rolled across the steel plate/adhesive/polyallomer composite twice. The composite, in which the epoxy adhesive layer was about 0.004 inch (0.1 mm) thick, was placed in an oven at ooo 170°F (77°C) for 2 hours. The oven was then turned off and o0 the composite was allowed to cool overnight (16 hours).

O 0 Adhesion was determined by pulling the polyallomer from o Q steel plate at a 90° angle and a rate of 12 inches (30 cm) per minute. No adhesive failure occurred. The polyallomer adherend failed at a force of about 40 lb/in (700 N/dm).

ooao aooa -9- Comparative Examples 1-3 In Comparative Examples 1-3, untreated polyallomer, polyallomer which had been corona-treated as in Example 1, and polyallomer which had been corona-treated and subjected to electron beam radiation as in Example 1 but with no monomer present, respectively were tested for adhesion as in Example 1. The results are shown in Table 1.

Example 2-19 In Examples 2-19, various monomers set forth in Table 1 were graft-polymerized onto polyallomer as described in Example 1 except thnat the monomer was applied by wiping the polyallomer with a paper towel moistened with the monomer and the dosage of electron beam irradiation was about 5 Mrads. In each of Examples 2-12 and 14-19, 95 parts by weight of the indicated monomer was mixed with 5 parts by weight trimethylolpropane triacrylate, as crosslinking agent and in Example 13 the trimethylolpropane triacrylate was applied as a 50 weight percent solution in acetone.

Composites were prepared as in Example 1 and tested for adhesion. The results are set forth in Table 1.

Table 1 Example Comp 1 Comp 2 Comp 3 2 3 4 0 5 6 7 8 9 10 11 12 13 14 0oi 16 17 18 19 Mon omier acrylic acid dimethylacrylamide diethylacrylamide dipropylacrylamide hydroxyethylacrylate butanedioldiacrylate hexanedioldiacrylate diethylaminoethylacrylate glycidyl methacrylate isobutylmethacrylate cyclohexylmethacrylate trimethyloipropane triacrylate t rime thyloipropane trimethacrylate pentaerythritol triacrylate pentaerythritol tetraacrylate hydantoin hexacrylate 2-vinyl-4 ,4 -dime thylazl ac tone N-vinylpyrrolidone Adhesion (N/din) 16 17

PAD

PAS

PAB

PAD

PAS

PAB

26

PAD

PAS

33

PAB

PAD

*polyallomer aO'herend break Examples 20 and 21 To 20 mil (0.5 mm) thick polyallrner sheet material was grafted a monomer mixture of 80 parts by weight diethylacrylamide, 20 parts by weight trimethylolpropane triacrylate, and 0.5 parts FC 430 as in Example 1.

rold-rolled mild steel plates (3"1 x 7"1 x 1/8"1 (7.5 cm x 17.5 -11cm x 2.2 cm) Type 1018 available from Paper Calmenson Co., St. Paul, Minnesota) were abraded by hand using Grade 36 sandpaper, followed by Grade 80 sandpaper, and then a Grade abrasive bristle brush, and then degreased with methyl ethyl ketone. The steel plates were then coated with Scotch-Weld R brand Epoxy Primer 1945, available from Minnesota Mining and Manufacturing Co., at a thickness of about 1-2 mil (0.025-0.05 mm) and allowed to dry for about ten minutes.

In Example 20, Scotch-Weld R brand Epoxy Adhesive rrt 1838-L B/A Translucent, available from Minnesota Mining and Manufacturing Co. was prepared by mixing equal volumes of 15 base and accelerator. The adhesive was coated on the primed ,i steel plate. The grafted surface of a 1 inch x 8 inch piece of the polyallomer was laid over the adhesive as in Example i 1 and a second steel plate was placed on top of the polyallomer to effect uniform contact between the polyallomer material and the adhesive, The thus-formed Scomposite was allowed to cure at room temperature (731F, 23 0 C) for three days, The top steel plate was then removed and the composite was soaked in water at room temperatu' for 13 days. When the composite was tested using t!: peel test as in Example 1, the polyallo.ei adherent i before any bond failure occurred, In Example 21 a composite was ripared ard t..

as in Example 20 except that the adhesiv' :sed was Scotch-Weld brand 2216 B/A Structural Adhesive (a parts by Svolume base mixed with 3 parts by volume accelerator).

Again, the polyallomer adherend broke before any bond failure occurred.

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Claims

1. An article comprising a polyolefin first substrate adhered to a second substrate coated with an epoxy adhesive, said polyolefin first substrate having graft-polymerized thereto at least one monomer selected from the group consisting of sulfonic and carboxylic acids and alkyl esters thereof containing fewer than eight carbon atoms in the ester group, amides and mono- and di-substituted amides, alcohols, amines, epoxides, and and 7-membered heterocyclic rings having at least one Soxygen and/or nitrogen atom in the ring, with the provisos that said monomer contain an ethylenically unsaturated polymerizable moiety and that said graft-polymerized monomers are in a layer less than 5 micrometers in thickness and contacting said epoxy adhesive.

2. The article of claim 1 wherein said graft-polymerized monomers are dimethylacrylamide and trimethylolpropane triacrylate.

3. The articles of claim 2 wherein said monomers are present in a ratio of 80 parts by weight dimethylacrylamide to 20 parts by weight trimethylolpropane triacrylate.

4. The article of claim 3 further comprising a wetting agent in said graft-polymerized layer. c 5. The article of claim 1 wherein said polyolefin first substrate is polyallomer.

6. The article of claim 1 wherein the thickness of said graft-polymerized monomer layer is less than about 1 micrometer. I Z-i A t v e f f/ ^y1 I 2 ~UII-i~LIII-_I~--. F -snuc- air~Y1 rr~- I- *ir~- 0 0 000 o 9 0 00 0 000000 0 0 0000 0oo 00 0 o j 0000 0 S000 0 0 0 0 00 03 GoI 00 0 0 0 000 o 0 0 0 9 09

7. The article of claim 1 wherein the thickness of said graft-polymerized Ifonomer layer is less than about micrometer.

8. The article of claim 1 wherein said second substrate is metallic.

9. The article of claim 1 wherein said article has a peel value of at least 25 lb/in (440 N/dm). The article of claim 1 wherein the strength of the bond between said epoxy and said graft-polyzmerized surface of said polyolefin substrate is greater than the strength of a polyallomer sheet having a thickness of millimeter.

11. An article comprising a polyolefin first substrate adhered to a second substrate with an epoxy resin adhesive, said polyolefin first substrate having graft-polymerized thereto at 1. one monomer selected from the group consisting of sulfonic and carboxylic acids and alkyl esters thereof containing fewer than eight carbon atoms in the ester group, amides and mono and di-substituted amides, ;alcohols, amines, epoxides, and and 7-membered heterocyclic rings having at least one oxygen and/or nitrogen atom in the ring, with the proviso that said monomer contain an ethylenically unsaturated polymerizable moiety and that said graft-polynmerized monomers are in a layer less than 5 micrometers in thickness, which awaft-polymerized monomer contacts said adhesive and provides a 900 peel back value of at least 25 lb/in (440 N/dm).

12. A method for adhering a polyolefin first substrate to a second substrate with an epoxy adhesive comprising the steps of -14 Ij a) coating on said polyolefin eirst substrate a liquid monomer selected from the group consisting of sulfonic and carboxylic acids and alkyl esters thereof containing fewer than eight carbon atoms in the ester group, amides and mono- and di-substituted amides, alcohols, amines, epoxides, and and I 7-membered heterocyclic rings having at least one oxygen and/or nitrogen atom in the ring, in a layerless than 5 micrometers in thickness, with the proviso that said monomer contain an ethylenically unsaturated polymerizable moiety; i b) irradiating the coated substrate with ionizing J .radiation to graft polymerize said monomer to said substrate; c) coating an epoxy adhesive on at least one of (i) said graft-polymerized monomer surface of said first j ssubstrate and (ii) a surface of said second substrate; d) contacting said surfaces and and e) curing said epoxy adhesive. i 13. The method of claim 12 wherein said monomer Sis coated at a thickness of less than about 1 micrometer.

14. The method of claim 12 wherein said monomer i is coated at a thickness of about 0.5 micrometer. I 15. The method of claim 12 wherein said ionizing Sradiation is electron beam radiation.

16. The method of claim 15 wherein said electron j beam radiation is at a dosage of 0.05 Mrads to 0.5 Mrads.

17. The method of claim 12 wherein said monomers are dimethylacrylamide and trimethylolpropane triacrylate. AA'\ @1< 1 I 18. The method of claim 17 wherein said monomers are present in a ratio of 80 parts by weight dimethylacrylamide to 20 parts by weight trimethlolpropane triacrylate. I 19. The method of claim 18 further comprising a wetting agent coated with said liquid monomer. j 20. The method of claim 12 further comprising i corona-treating said polyolefin first substrate prior to I coating said polyolefin first substrate with said liquid monomer. i 21. An article comprising a polyolefin first substrate adhered to a second substrate coated with an epoxy adhesive, substantially as defined herein with reference to the Examples other than comparative examples.

22. A method for adhering a polyolefin first substrate to a second substrate with an epoxy adhesive substantially as described herein with reference to the Examples other than comparative examples. DATED this TWENTY SECOND day of MAY 1990 Minnesota Mining and Manufacturing Company Patent Attorneys for the Applicant SPRUSON FERGUSON I 1 I 1 1