Patent Application
20220411676
The present invention relates to an adhesive composition and a laminate.
Polyolefin-based resins, such as polypropylene and polyethylene, have been recently widely used as sheets, films, molded articles, and the like because they are inexpensive and have many excellent properties, such as moldability, chemical resistance, water resistance, and electrical characteristics.
However, unlike polar substrates of, for example, polyurethane-based resins, polyamide resins, acrylic resins, and polyester resins, substrates made of polyolefin-based resins (referred to below as “polyolefin-based substrates”) are nonpolar and crystalline and thus have the disadvantage that coating and bonding are difficult.
In recent years, there has been a growing demand for excellent adhesion not only between polyolefin-based substrates, but also between a polyolefin-based substrate and a different type of material, such as a polar plastic substrate (e.g., vinyl chloride (PVC) or polyester) or a metal.
As the main component of an adhesive between a polyolefin-based resin substrate and a different type of material, an adhesive composition containing a thermoplastic linear copolymer as a base resin, a modified polyolefin resin, and a tackifier (Patent Literature (PTL) 1), an adhesive composition containing a modified polyolefin, an aliphatic polyester-based resin, an olefin-based resin, and a tackifier (PTL 2), an adhesive composition containing a modified polyolefin, a thermoplastic resin, and a tackifier (PTL 3), and the like have been proposed.
PTL 1: JP2004-292716A
PTL 2: JP2014-234400A
PTL 3: JP2016-089060A
However, although all of the adhesive compositions proposed above show good adhesion between a polyolefin resin substrate and a metal (aluminum) and between a polyolefin resin substrate and a polyester (PET) substrate, the adhesion between a substrate other than aluminum or PET and a polyolefin resin substrate is unknown. In addition, they are all hot-melt adhesives, which require bonding at a high temperature of 180° C. An object of the present invention is to provide an adhesive composition that shows good adhesion between polyolefin resin substrates and various polar plastic substrates or metal substrates other than polyolefin resin substrates and that enables bonding at low temperatures.
To achieve the above object, the present inventors conducted extensive research and found that a specific combination of a modified polyolefin and an ethylene-α-olefin-diene rubber is effective. The present invention was thus proposed. Specifically, the present invention includes the following.
(1) An adhesive composition comprising an acid-modified polyolefin (A) and an ethylene-α-olefin-diene rubber (B), the ethylene-α-olefin-diene rubber (B) being present in an amount of 1 to 100 parts by mass per 100 parts by mass of the acid-modified polyolefin (A).
(2) An adhesive composition,
wherein the ethylene-α-olefin-diene rubber (B) has a weight average molecular weight (Mw) of 1,000 or more and 100,000 or less.
(3) The adhesive composition according to Item (1) or (2), wherein the acid-modified polyolefin (A) has an acid value of 2 to 50 mgKOH/g.
(4) The adhesive composition according to Items (1) to (3), further comprising a solvent (C).
(5) The adhesive composition according to any one of Items (1) to (4), wherein the solvent (C) comprises an alicyclic hydrocarbon solvent (C1) and an ester-based solvent or ketone-based solvent (C2).
(6) The adhesive composition according to any one of Items (1) to (5), wherein the mass ratio of the alicyclic hydrocarbon solvent (C1) to the ester-based solvent or ketone-based solvent (C2), (C1)/(C2), is 95/5 to 50/50.
(7) The adhesive composition according to any one of Items (1) to (6) for use in bonding a polyolefin resin substrate 1 and a substrate 2 different from the substrate 1.
(8) The adhesive composition according to any one of Items (1) to (7), wherein the acid-modified polyolefin (A) comprises propylene in an amount of 60 mol % or more.
(9) A laminate comprising a polyolefin resin substrate 1 and a substrate 2 different from the substrate 1, the substrate 1 and the substrate 2 being bonded with the adhesive composition according to any one of Items (1) to (8).
The adhesive composition of the present invention comprises an acid-modified polyolefin and an ethylene-α-olefin-diene rubber (B) and exhibits good elongation and excellent adhesion between a nonpolar substrate, such as polyolefin, and a different type of substrate, such as an acrylonitrile-butadiene-styrene copolymer (ABS), polycarbonate (PC), or like polar substrates, or metal, even when no curing agent is used. Moreover, since the adhesive composition can be applied by using a dry lamination process, equipment costs can be reduced, and the film thickness can be made thin. Further, the adhesive composition exhibits excellent adhesion even when heat bonding is performed at a low temperature of, for example, 90° C. or less, at which the thermal shrinkage effect on polyolefin substrates is small.
The adhesive composition of the present invention exhibits good adhesion not only to polyolefin substrates, but also to substrates of ABS resins, polycarbonates, polyethylene terephthalate (PET), polyvinyl chloride (PVC), acrylic resins, aluminum, and the like, and is thus useful as an adhesive for multi-substrates.
Further, since the adhesive composition of the present invention does not contain a curing agent, it can be easily peeled off from substrates by heat treatment even after bonding.
Embodiments of the present invention are described in detail below.
The acid-modified polyolefin (A) used in the present invention is not limited and is preferably obtained by grafting polypropylene with at least one of α,β-unsaturated carboxylic acid and acid anhydride thereof.
As polypropylene, homopolypropylene can be particularly preferably used, and a propylene-α-olefin copolymer can also be used. The propylene-α-olefin copolymer mainly comprises propylene that is copolymerized with an α-olefin. Examples of α-olefins include ethylene, 1-butene, 1-heptene, 1-octene, 4-methyl-1-pentene, vinyl acetate, and the like. These α-olefins can be used singly or in a combination of two or more. Preferred among these α-olefins are ethylene and 1-butene.
The acid-modified polyolefin (A) preferably contains, as an olefin component, propylene in an amount of 60 mol % or more, more preferably 70 mol % or more, even more preferably 80 mol % or more, and still even more preferably 90 mol % or more. The higher the propylene content, the better the adhesion to propylene substrates.
The molar ratio of propylene to 1-butene is preferably such that propylene/1-butene=100 to 60/0 to 40, more preferably 98 to 65/2 to 35, and even more preferably 90 to 70/10 to 30. When the molar percentage of propylene is 60% or more, excellent adhesion to polyolefin substrates is exhibited.
The total amount of the propylene component and the 1-butene component as olefin components is preferably 50 parts by mass or more, more preferably 55 parts by mass or more, even more preferably 60 parts by mass or more, and particularly preferably 65 parts by mass or more, based on the resin components taken as 100 parts by mass. The total amount of the propylene component and the 1-butene component may be 70 parts by mass. When the total amount of the propylene component and the 1-butene component is 50 parts by mass or more, the adhesion to polyolefin substrates is particularly good.
Examples of the at least one of α,β-unsaturated carboxylic acid and acid anhydride thereof include maleic acid, itaconic acid, citraconic acid, and acid anhydrides thereof. Among these, the acid anhydrides are preferable, and maleic anhydride is more preferable. Specific examples include maleic anhydride-modified polypropylene, maleic anhydride-modified propylene-ethylene copolymers, maleic anhydride-modified propylene-1-butene copolymers, maleic anhydride-modified propylene-ethylene-1-butene copolymers, and the like. These acid-modified polyolefins can be used singly, or in a combination of two or more. Among these, maleic anhydride-modified polypropylene is preferable.
The acid-modified polyolefin (A) preferably has an acid value of 2 to 50 mgKOH/g, more preferably 3 to 40 mgKOH/g, even more preferably 5 to 30 mgKOH/g, and particularly preferably 5 to 16 mgKOH/g. When the acid value is 2 mgKOH/g or more, the adhesive layer exhibits good elongation. When the acid value is 50 mgKOH/g or less, the solution stability at low temperatures tends to be good.
The acid-modified polyolefin (A) may be chlorinated.
The melting point (Tm) of the acid-modified polyolefin (A) is preferably 50° C. or more and 130° C. or less. The melting point (Tm) of the acid-modified polyolefin (A) is more preferably 55° C. or more, and even more preferably 60° C. or more. The melting point (Tm) of the acid-modified polyolefin (A) is also more preferably 125° C. or less, even more preferably less than 120° C., still even more preferably 115° C. or less, and most preferably 110° C. or less. When the melting point is 50° C. or more, strong cohesive force derived from crystals is attained, and good adhesion is achieved. When the melting point is 130° C. or less, solution stability and flowability are good, and operability during bonding is excellent. In addition, bonding can be performed even at low temperatures.
The acid-modified polyolefin (A) preferably has a heat of fusion of 20 to 70 J/g, more preferably 25 to 65 J/g, and most preferably 30 to 60 J/g. When the heat of fusion is not less than the lower limit, strong cohesive force derived from crystals is attained, and good adhesion is achieved. When the heat of fusion is less than the upper limit, gelation is less likely to occur, and good solution stability is attained.
The acid-modified polyolefin (A) preferably has a weight average molecular weight (Mw) of 10,000 to 200,000, more preferably 20,000 to 180,000, even more preferably 30,000 to 160,000, particularly preferably 40,000 to 140,000, and most preferably 50,000 to 100,000. When the weight average molecular weight is 10,000 or more, strong cohesive force is attained, and good adhesion is achieved. When the weight average molecular weight is 200,000 or less, flowability is high, resulting in good operability during bonding, and good solution stability at low temperatures is attained.
The method for producing the acid-modified polyolefin (A) is not particularly limited. Examples of the method include a radical grafting reaction in which a radical species is formed in a polymer serving as a main chain, and unsaturated carboxylic acid and acid anhydride are graft-polymerized using the radical species as a polymerization starting point; and the like.
The radical generator is not particularly limited, and is preferably an organic peroxide. Examples of organic peroxides include, but are not limited to, peroxides, such as di-tert-butyl peroxyphthalate, tert-butyl hydroperoxide, dicumyl peroxide, benzoyl peroxide, tert-butyl peroxybenzoate, tert-butyl peroxy-2-ethylhexanoate, tert-butyl peroxypivalate, methyl ethyl ketone peroxide, di-tert-butyl peroxide, and lauroyl peroxide; azonitriles, such as azobisisobutyronitrile and azobisisopropionitrile; and the like.
These acid-modified polyolefins (A) may be used singly or in a combination of two or more.
The adhesive composition of the present invention contains an ethylene-α-olefin-diene rubber (B). The presence of the ethylene-α-olefin-diene rubber reduces the internal stress after formation of an adhesive film and imparts tackiness, thereby improving adhesion to substrates.
The ethylene-α-olefin-diene rubber (B) preferably contains ethylene in an amount of 30 mass % or more, more preferably 35 mass % or more, and even more preferably 40 mass % or more. The ethylene-α-olefin-diene rubber (B) also preferably contains ethylene in an amount of 95 mass % or less, more preferably 90 mass % or less, even more preferably 850 mass % or less, and particularly preferably 80 mass % or less.
Examples of the α-olefin component of the ethylene-α-olefin-diene rubber (B) include C3-20 olefins. These olefins can be used singly or in a combination of two or more. As the α-olefin, propylene is preferable, and only propylene is more preferable.
The amount of the diene component in the ethylene-α-olefin-diene rubber (B) is preferably 3 mass % or more, more preferably 6 mass % or more, and even more preferably 8 mass % or more. The amount of the diene component in the ethylene-α-olefin-diene rubber (B) is also preferably 30 mass % or less, more preferably 20 mass % or less, even more preferably 15 mass % or less, and particularly preferably 12 mass % or less.
The ethylene-α-olefin-diene rubber (B) preferably has a weight average molecular weight (Mw) of 10,000 or more and 200,000 or less, more preferably 15,000 or more and 180,000 or less, even more preferably 20,000 or more and 160,000 or less, particularly preferably 30,000 or more and 140,000,0 or less, still even more preferably 40,000 or more and 120,000 or less, and most preferably 45,000 or more and 100,000 or less. When the weight average molecular weight is 10,000 or more, the compatibility with the acid-modified polyolefin (A) is favorable, a stress relaxation effect is exhibited, and adhesion tends to be good. When the weight average molecular weight is 100,000 or less, the compatibility with the acid-modified polyolefin (A) is significantly improved.
The amount of the ethylene-α-olefin-diene rubber (B) added is preferably 1 part by mass or more and 100 parts by mass or less, more preferably 5 parts by mass or more and 80 parts by mass or less, even more preferably 8 parts by mass or more and 75 parts by mass or less, particularly preferably 12 parts by mass or more and 70 parts by mass or less, and still even more preferably 15 parts by mass or more and 65 parts by mass or less, and most preferably 18 parts by mass or more and 60 parts by mass or less, per 100 parts by weight of the acid-modified polyolefin (A). When the amount of the ethylene-α-olefin-diene rubber (B) is 1 part by mass or more, the compatibility with the acid-modified polyolefin (A) is favorable, a stress relaxation effect is exhibited, and adhesion tends to be good. When the amount of the ethylene-α-olefin-diene rubber (B) is 100 parts by mass or less, favorable tackiness is exhibited, and adhesion is improved.
The ethylene-α-olefin-diene rubber (B) may be in any form. The ethylene-α-olefin-diene rubber (B) is particularly preferably semi-solid or liquid at room temperature. When a coating film is formed, high adhesion and good elongation are achieved.
The viscosity of the ethylene-α-olefin-diene rubber (B) at 60° C. is preferably 100 Pa·S or more and 2,000 Pa·S or less, more preferably 200 Pa·S or more and 1,800 Pa·S or less, even more preferably 300 Pa·S or more and 1,600 Pa·S or less, particularly preferably 400 Pa·S or more and 1,500 Pa·S or less, still even more preferably 500 Pa·S or more and 1,400 Pa·S or less, and most preferably 600 Pa·S or more and 1,300 Pa·S or less. When the viscosity is 100 Pa·S or more, adhesion is exhibited. When the viscosity is 2,000 Pa·S or less, the compatibility with other components is good.
The adhesive composition of the present invention may contain a solvent (C). The solvent (C) is not particularly limited as long as it can dissolve or disperse the acid-modified polyolefin (A) and the ethylene-α-olefin-diene rubber (B). An alicyclic hydrocarbon solvent (C1) and an ester-based solvent or ketone-based solvent (C2) are preferable.
Examples of the alicyclic hydrocarbon solvent (C1) include cyclohexane, methylcyclohexane, ethylcyclohexane, and the like. Examples of the ester-based solvent or ketone-based solvent (C2) include ethyl acetate, propyl acetate, butyl acetate, methyl ethyl ketone, and the like. Among these, methylcyclohexane and methyl ethyl ketone are preferable. These may be used singly or in a combination of two or more.
The solvent (C) for use in the present invention may be a mixed solvent containing the alicyclic hydrocarbon solvent (C1) and the ester-based solvent or ketone-based solvent (C2). Using a mixed solvent of the alicyclic hydrocarbon solvent and the ester-based solvent or ketone-based solvent improves the solubility of the adhesive composition.
When the mixed solvent is used, the mass ratio of the alicyclic hydrocarbon solvent (C1) to the ester-based solvent or ketone-based solvent (C2), (C1)/(C2), is preferably within the range of 99/1 to 50/50, more preferably 95/5 to 60/40, and particularly preferably 90/10 to 70/30. If the amount of the alicyclic hydrocarbon (C1) is larger than the above range, the viscosity may be high, and coating unevenness may occur, resulting in a decrease in adhesion. When the alicyclic hydrocarbon (C1) in the above range is contained, the solubility of the resins is good.
The solvent (C) may be contained in an amount of 10 to 2000 parts by mass per 100 parts by mass of the acid-modified polyolefin (A). The amount of the solvent (C) is preferably 25 parts by mass or more and 1500 parts by mass or less, more preferably 50 parts by mass or more and 1000 parts by mass or less, even more preferably 100 parts by mass or more and 900 parts by mass or less, and still even more preferably 100 parts by mass or more and 800 parts by mass or less, per 100 parts by mass of the acid-modified polyolefin (A). When the amount of the solvent (C) is within the above range, it is advantageous in terms of production and transportation costs.
The adhesive composition of the present invention may contain various additives, such as plasticizers, curing accelerators, flame retardants, pigments, and antiblocking agents, in addition to the acid-modified polyolefin (A) and the ethylene-α-olefin-diene rubber (B), as long as the performance of the present invention is not impaired.
The adhesive composition of the present invention preferably contains the acid-modified polyolefin (A) and the ethylene-α-olefin-diene rubber (B) in a total amount of 5 mass % or more and 40 mass % or less. The total amount of the acid-modified polyolefin (A) and the ethylene-α-olefin-diene rubber (B) in the adhesive composition is more preferably 7 mass % or more, even more preferably 10 mass % or more, and particularly preferably 13 mass % or more. The total amount of the acid-modified polyolefin (A) and the ethylene-α-olefin-diene rubber (B) in the adhesive composition is also preferably 40 mass % or less, more preferably 35 mass % or less, even more preferably 30 mass % or less, and particularly preferably 25 mass % or less. When the total amount of the acid-modified polyolefin (A) and the ethylene-α-olefin-diene rubber (B) in the adhesive composition is within the above range, the storage stability is good, and the coating properties tend to be good.
The curing agent is not particularly limited and generally refers to a known curing agent. Examples include epoxy curing agents, isocyanate curing agents, oxazoline group-containing or carbodiimide group-containing compounds, silane coupling agents, and the like.
The laminate of the present invention is one in which a polyolefin resin substrate 1, and a polyolefin substrate 1 or a different type of substrate 2 are laminated using the adhesive composition of the present invention. The different type of substrate 2 is a substrate different from the polyolefin substrate 1. For example, if the polyolefin substrate 1 is polypropylene, the different type of substrate 2 is an ABS resin, a polycarbonate, or the like other than polypropylene.
The laminate of the present invention is useful, for example, for vehicle parts, such as automobile parts (e.g., bumpers, instrument panels, trim, and garnishes) and interior materials of bullet trains; home appliance parts such, as TVs, washing machines, refrigerator parts, air conditioner parts, and vacuum cleaner parts; mobile devices and communication devices, such as mobile phone devices and notebook computers; touch panels for various devices; and daily necessities.
The lamination may be performed using a previously known laminate production technique. Although there is no particular limitation, for example, the adhesive composition may be applied to the surface of a substrate using a suitable coating means, such as an applicator or a bar coater, followed by drying. After drying, another substrate may be stacked and bonded (laminate bonding or heat seal bonding) to the coating surface while the layer of the adhesive composition (adhesive layer) formed on the surface of the substrate is in a molten state, to thus obtain a laminate. Sufficient adhesion can be ensured when either laminate bonding or heat seal bonding is used as the method for producing the laminate.
The thickness of the adhesive layer formed from the adhesive composition is not particularly limited, and is preferably 0.5 to 60 μm, more preferably 1 to 50 μm, and even more preferably 2 to 40 μm.
The polyolefin resin substrate may be suitably selected from previously known polyolefin resins. For example, polyethylene, polypropylene, ethylene-propylene copolymers, and the like may be used without limitation. Among these, it is preferable to use a cast polypropylene film (also referred to below as “CPP”). The thickness of the polyolefin resin substrate is not particularly limited, and is preferably 20 to 100 μm, more preferably 25 to 95 μm, and even more preferably 30 to 90 μm. The polyolefin resin substrate may contain a pigment and various additives or may be subjected to surface treatment, if necessary.
The polyolefin resin substrate may be suitably selected from previously known polyolefin resins. For example, polyethylene, polypropylene, ethylene-propylene copolymers, and the like may be used without limitation. Among these, it is preferable to use a polypropylene test plate. The thickness of the polyolefin resin substrate is not particularly limited, and is preferably 0.1 to 100 mm, more preferably 0.5 to 90 mm, and even more preferably 1 to 80 mm. The polyolefin resin substrate may contain a pigment and various additives or may be subjected to surface treatment, if necessary.
The different type of substrate may be a film or a molded article. ABS resins, polycarbonates, polyvinyl chloride, acrylic resins, Al foil, and the like can be used. Although there is no particular limitation, commercially available test plates can be used. The thickness of the different type of substrate is not particularly limited, and is preferably 0.1 to 100 mm, more preferably 0.5 to 90 mm, and even more preferably 1 to 80 mm. The different type of substrate may be subjected to surface treatment or may be untreated. In either case, comparable effects can be exhibited.
The present invention is described in detail below with reference to Examples; however, the present invention is not limited to these Examples.
100 parts by mass of polypropylene (Tm: 80° C.; weight average molecular weight: 135,000), 150 parts by mass of toluene, 8.5 parts by mass of maleic anhydride, and 4 parts by mass of di-tert-butyl peroxide were placed in a 1-L autoclave. The mixture was heated to 140° C. and then further stirred for 1 hour. After the reaction was completed, the reaction liquid was poured into a large amount of methyl ethyl ketone to deposit the resin. This resin was further washed several times with methyl ethyl ketone to remove unreacted maleic anhydride. The resulting resin was dried under reduced pressure to thus obtain a maleic anhydride-modified polypropylene (A-1; acid value: 12 mgKOH/g-resin; weight average molecular weight: 60,000; Tm: 80° C.; heat of fusion: 31 J/g), which is an acid-modified polyolefin.
A maleic anhydride-modified polypropylene (A-2; acid value: 12 mgKOH/g-resin; weight average molecular weight: 45,000; Tm: 80° C.; heat of fusion: 33.5 J/g), which is an acid-modified polyolefin, was obtained in the same manner as in Production Example 1, except that another polypropylene (Tm: 80° C.; weight average molecular weight: 45,000) was used in place of the polypropylene used in Production Example 1.
A maleic anhydride-modified propylene-butene copolymer (A-3; acid value: 12 mgKOH/g-resin; weight average molecular weight: 90,000; Tm: 80° C.; heat of fusion: 47.9 J/g), which is an acid-modified polyolefin, was obtained in the same manner as in Production Example 1, except that a propylene-butene copolymer (Tm: 83° C.; propylene: 80 mol %; butene: 20 mol %) was used in place of the polypropylene used in Production Example 1.
A maleic anhydride-modified propylene-butene copolymer (A-4; acid value: 12 mgKOH/g-resin; weight average molecular weight: 90,000; Tm: 95° C.; heat of fusion: 55.7 J/g), which is an acid-modified polyolefin, was obtained in the same manner as in Production Example 1, except that a propylene-butene copolymer (Tm: 98° C.; propylene: 85 mol %; butene: 15 mol %) was used in place of the polypropylene used in Production Example 1, and the amount of maleic anhydride was 12 parts by mass.
83 parts by mass of the maleic anhydride-modified polypropylene (A-1) obtained in Production Example 1, 17 parts by mass of an ethylene-α-olefin-diene rubber (EPDM) (B-1), 540 parts by mass of cyclohexane, and 60 parts by mass of methyl ethyl ketone were placed in a 500-ml four-necked flask equipped with a water-cooled reflux condenser and a stirrer. The mixture was heated to 70° C. with stirring, followed by continuous stirring for 1 hour. The mixture was then cooled to obtain an adhesive composition 1. A laminate was produced using the adhesive composition 1 by the following method.
A cast polypropylene film (Pylen (registered trademark) Film-CT produced by Toyobo Co., Ltd.; thickness: 80 μm) (which may be referred to below as “CPP”) was used as a polyolefin resin substrate. The obtained adhesive composition was applied to the polyolefin resin substrate with an applicator so that the film thickness of the adhesive layer after drying was 20 μm. The coating surface was dried with a hot air dryer at 100° C. for 3 minutes to obtain the polyolefin resin substrate on which an adhesive layer having a film thickness of 20 μm was laminated. A polypropylene (PP) test plate (produced by Nippon Testpanel Co., Ltd.; thickness: 2 mm), an ABS test plate (produced by Nippon Testpanel Co., Ltd.: thickness: 2 mm), and a polycarbonate (PC) test plate (produced by Nippon Testpanel Co., Ltd.; thickness: 2 mm) were bonded to the surface of the adhesive layer at a heat-sealing temperature of 90° C. (55° C. on the test plate side) and 0.3 MPa for 15 seconds using a heat seal tester (TP-701-B) produced by Tester Sangyo Co., Ltd., followed by aging at room temperature for one day, thereby obtaining laminates. The adhesion in the obtained laminates was evaluated. Table 1 shows the results.
Adhesive compositions 2 to 11 were produced in the same manner as in Example 1, except that the acid-modified polyolefins (A) and the ethylene-α-olefin-diene rubbers (B) shown in Table 1 were used. Laminates were produced using the obtained adhesive compositions 2 to 11 in the same manner as in Example 1, and adhesion evaluation was performed. Table 1 shows the evaluation results.
The ethylene-α-olefin-diene rubbers (B) shown in Table 1 are as follows.
B-1: Trilene (registered trademark) 65 (Mw: 47,000; ethylene-propylene-diene rubber; diene component: 10 mass %) produced by Lion Elastomers
B-2: Trilene (registered trademark) 67 (Mw: 39,000; ethylene-propylene-diene rubber; diene component: 9.5 mass %) produced by Lion Elastomers
B-3: Trilene (registered trademark) 77 (Mw: 27,000; ethylene-propylene-diene rubber; diene component: 10.5 mass %) produced by Lion Elastomers
A laminate of a polyolefin resin substrate (CPP film) and an aluminum substrate (produced by Nippon Testpanel Co., Ltd.; thickness: 2 mm) was produced using the adhesive composition 1 of Example 1 by the method described in the production of a laminate (heat seal bonding) described above. The adhesive composition 1 achieved good adhesion (peel strength) of 10 N/15 mm. The adhesive compositions 2 to 11 also achieved good adhesion.
Analytical measurement and evaluation of the thus-obtained acid-modified polyolefins, stress relaxing agents, tackifiers, adhesive compositions, and laminates were performed in the following manner.
The acid value (mgKOH/g-resin) in the present invention refers to the amount of KOH required to neutralize 1 g of acid-modified polyolefin (A), and was measured in accordance with the test method of JIS K0070 (1992). Specifically, 1 g of the acid-modified polyolefin was dissolved in 100 g of xylene adjusted to a temperature of 100° C., and then titrated with a 0.1 mol/L potassium hydroxide ethanol solution (trade name: 0.1 mol/L Potassium Hydroxide Ethanolic Solution, produced by Wako Pure Chemical Industries, Ltd.) using phenolphthalein as an indicator at the same temperature. The amount of potassium hydroxide required for titration was converted into milligrams to calculate the acid value (mgKOH/g).
The weight average molecular weight in the present invention is a value measured with an Alliance e2695 gel permeation chromatograph (referred to below as “GPC”; standard substance: polystyrene resin, mobile phase: tetrahydrofuran, column: Shodex KF-806 and KF-803, column temperature: 40° C., flow rate: 1.0 ml/min, detector: photodiode array detector (wavelength: 254 nm=ultraviolet light)) produced by Nihon Waters K.K.
The melting point and heat of fusion in the present invention are values measured with a differential scanning calorimeter (referred to below as “DSC”; Q-2000 produced by TA Instruments Japan Inc.) from the top temperature and area of the melting peak when a sample is maintained at −50° C. for 5 minutes, melted by heating at a rate of 10° C./min, maintained at 200° C. for 2 minutes, cooled to −50° C. at a rate of 10° C./min to achieve resinification, and melted again by heating at a rate of 10° C./min.
The laminates were cut into 15-mm strips, and adhesion was evaluated using a 180° peel test according to the following criteria.
In the 180° peel test, the peel strength was measured at a tensile rate of 50 mm/min at 25° C. in accordance with the test method of ASTM-D1876-61 by using a Tensilon RTM-100 produced by Orientec Corporation. The average of two test values was defined as the peel strength (N/15 mm) between a polyolefin resin substrate and a different type of substrate.
The elongation of a coating film in the present invention was determined by preparing a cast film with a thickness of 50 μm and performing measurement at a tensile rate of 50 mm/min at 25° C. by using a Tensilon RTM-100 produced by Orientec Corporation. The cast film was prepared in the following manner. Each of the obtained adhesive compositions was individually applied to a Teflon sheet with an applicator so that the film thickness of the adhesive layer after drying was 50 μm. The coating surface was dried with a hot air dryer at 100° C. for 10 minutes to obtain the Teflon sheet on which an adhesive layer having a film thickness of 50 μm was laminated. The coating film was peeled off from the Teflon sheet and cut to a size of 60 long×15 mm wide. The distance between chucks (initial length of the coating film) was set to 30 mm, and the elongation was calculated according to the following formula.
{(length of coating film at break−initial length of coating film)/initial length of coating film}×100(%)
From the evaluation of adhesion and elongation in the present invention, evaluation was performed according to the following criteria.
A: The average of adhesion (peel strengths) to the three substrates (PP, ABS, and PC) was 14 (N/15 mm) or more, and the elongation (elongation at break) was 550 (% GL) or more.
B: (i) The average of adhesion (peel strengths) to the three substrates (PP, ABS, and PC) was 7 (N/15 mm) or more, and the elongation (elongation at break) was less than 550 (% GL) and 350 (% GL) or more, or (ii) the average of adhesion (peel strengths) to the three substrates (PP, ABS, and PC) was less than 14 (N/15 mm) and 7 (N/15 mm) or more, and the elongation (elongation at break) was 550 (% GL) or more.
C: The average of adhesion (peel strengths) to the three substrates (PP, ABS, and PC) was less than 7 (N/15 mm), or the elongation (elongation at break) was less than 350 (% GL).
The adhesive composition of the present invention contains an acid-modified polyolefin and a thermoplastic resin, and exhibits excellent adhesion between a nonpolar substrate, such as a polyolefin, and a different type of substrate, such as a polar substrate or a metal, even when no curing agent is used. Moreover, since the adhesive composition can be applied by using a dry lamination process, equipment costs can be reduced, and the film thickness can be made thin. Further, the adhesive composition exhibits excellent adhesion and good elongation even when heat bonding is performed at a low temperature of, for example, 90° C. or less, at which the thermal shrinkage effect on polyolefin substrates is small. Thus, the adhesive composition of the present invention can be widely used as an adhesive for various applications, including for decorative films and paint films, in which various types of substrates are bonded together.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-216781 | Nov 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/042128 | 11/11/2020 | WO |
