JP2009242512A - Adhesive composition - Google Patents
Adhesive composition Download PDFInfo
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- JP2009242512A JP2009242512A JP2008089256A JP2008089256A JP2009242512A JP 2009242512 A JP2009242512 A JP 2009242512A JP 2008089256 A JP2008089256 A JP 2008089256A JP 2008089256 A JP2008089256 A JP 2008089256A JP 2009242512 A JP2009242512 A JP 2009242512A
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- adhesive composition
- vinyl acetate
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Abstract
Description
本発明はホルムアルデヒド含有樹脂を使用することなく、干割れしやすい突板であっても干割れを防止でき、突板の接着に適した接着剤組成物に関する。 The present invention relates to an adhesive composition that can prevent dry cracking even if it is a veneer that is prone to dry cracking without using a formaldehyde-containing resin, and is suitable for adhesion of the veneer.
従来、合板などの木質基材に対して化粧紙や突板を接着する際には、尿素やメラミンとホルムアルデヒドを縮重合したアミノ系樹脂と酢酸ビニル系樹脂を混合した接着剤が用いられてきた。しかしながら、いわゆるシックハウス症候群の問題により、ホルムアルデヒドを一定量以上放散する建材は使用面積が制限される等、建材やこれに使用される接着剤はホルムアルデヒドを使用しないタイプのものが求められるようになった。 Conventionally, when a decorative paper or a veneer is bonded to a woody substrate such as plywood, an adhesive obtained by mixing an amino resin obtained by condensation polymerization of urea, melamine and formaldehyde and a vinyl acetate resin has been used. However, due to the problem of so-called sick house syndrome, building materials that dissipate more than a certain amount of formaldehyde have a limited use area. For example, building materials and adhesives used in these materials are required to be of a type that does not use formaldehyde. .
本発明者らは既にアミノ系樹脂を使用しないタイプの接着剤を提案しているが、メープル、松やケヤキのような干割れしやすい突板を接着した際は干割れが生じていた。
本発明はアミノ系樹脂のようなホルムアルデヒド含有樹脂を使用することなく、干割れしやすい突板であっても干割れを防止できる接着剤組成物を提供するものである。 This invention provides the adhesive composition which can prevent a dry crack even if it is a veneer which is easy to dry without using formaldehyde containing resin like an amino-type resin.
本発明者らが鋭意検討を重ねた結果、酢酸ビニル系樹脂エマルジョン(a)、ポリビニルアルコール(b)、水性エポキシ化合物(c)を含有することを特徴とする接着剤組成物により前記課題が解決されることを見出した。また、さらにイソシアネート化合物(d)を含有することが好ましく、前記ポリビニルアルコール(b)が、アセトアセチル基を含有することが好ましいことを併せて見出した。 As a result of intensive studies by the present inventors, the above problem is solved by an adhesive composition comprising a vinyl acetate resin emulsion (a), polyvinyl alcohol (b), and an aqueous epoxy compound (c). I found out that Moreover, it was found that the isocyanate compound (d) was further contained, and that the polyvinyl alcohol (b) preferably contained an acetoacetyl group.
本発明の接着剤組成物が干割れしやすい突板であっても干割れを防止できる理由は必ずしも定かではないが、突板に対して十分に強固な接着力を有する一方、突板の乾燥収縮による動きを緩和できる柔軟さを併せ持つことによるものと考えられる。 Although the reason why the adhesive composition of the present invention can prevent dry cracking even if it is a veneer that is prone to dry cracks is not necessarily clear, it has a sufficiently strong adhesive force to the veneer, while it moves due to dry shrinkage of the veneer. This is thought to be due to having the flexibility to alleviate the problem.
本発明の接着剤組成物は干割れしやすい突板であっても干割れを防止できるため、メープル、松やケヤキのような干割れしやすい突板でも問題なく接着することができる。また、ホルムアルデヒドの放散源となるアミノ系樹脂を使用していないため、住宅等に使用される建材の製造にも問題なく使用できる。 Since the adhesive composition of the present invention can prevent dry cracking even if it is a veneer that is prone to dry cracking, it can be bonded without problems even if it is a dry veneer such as maple, pine or zelkova. In addition, since no amino-based resin, which is a formaldehyde emission source, is used, it can be used without problems in the production of building materials used in houses and the like.
以下、本発明について詳細に説明する。 Hereinafter, the present invention will be described in detail.
本発明で用いる酢酸ビニル系樹脂エマルジョン(a)は、通常、ケン化度75〜99.5%、平均重合度300〜4000であるポリビニルアルコールのような水溶性高分子を保護コロイドとし、必要によって界面活性剤等の乳化剤を併用して、酢酸ビニル単独または酢酸ビニルと共重合可能な単量体を乳化重合することにより合成される。酢酸ビニルと共重合可能な単量体として、エチレン、アクリル酸、アクリル酸エステル類、バーサチック酸ビニルなどが挙げられる。エチレンと共重合したエチレン−酢酸ビニル共重合樹脂はガラス転移温度が低く柔軟であり、これを用いることが好ましい。また、エチレン−酢酸ビニル共重合樹脂エマルジョンやアクリル系樹脂エマルジョンのようにガラス転移温度が低い樹脂エマルジョンの存在下において、酢酸ビニル単独または酢酸ビニルと共重合可能な単量体を重合することにより、柔軟な酢酸ビニル系樹脂エマルジョンを得られ、これを用いることができる。さらに、カルボキシル基含有単量体やアセトアセチル基含有単量体を共重合した酢酸ビニル系樹脂エマルジョンを用いることにより、耐水性を向上することができる。 The vinyl acetate resin emulsion (a) used in the present invention usually has a water-soluble polymer such as polyvinyl alcohol having a saponification degree of 75 to 99.5% and an average polymerization degree of 300 to 4000 as a protective colloid. It is synthesized by emulsion polymerization of vinyl acetate alone or a monomer copolymerizable with vinyl acetate in combination with an emulsifier such as a surfactant. Examples of monomers copolymerizable with vinyl acetate include ethylene, acrylic acid, acrylic esters, and vinyl versatate. An ethylene-vinyl acetate copolymer resin copolymerized with ethylene has a low glass transition temperature and is flexible and is preferably used. In addition, by polymerizing vinyl acetate alone or a monomer copolymerizable with vinyl acetate in the presence of a resin emulsion having a low glass transition temperature such as an ethylene-vinyl acetate copolymer resin emulsion or an acrylic resin emulsion, A flexible vinyl acetate resin emulsion can be obtained and used. Furthermore, water resistance can be improved by using a vinyl acetate resin emulsion copolymerized with a carboxyl group-containing monomer or an acetoacetyl group-containing monomer.
ポリビニルアルコール(b)は、前記酢酸ビニル系樹脂エマルジョン中にも含まれるものであるが、酢酸ビニルなどの重合の際に保護コロイドとして消費されるため、重合後に別途添加されたポリビニルアルコールを示すものである。また、アセトアセチル基含有ポリビニルアルコールを用いることによって耐水性を向上させることができる。 Polyvinyl alcohol (b), which is also contained in the vinyl acetate resin emulsion, is consumed as a protective colloid during the polymerization of vinyl acetate or the like, and thus indicates polyvinyl alcohol added separately after polymerization. It is. Moreover, water resistance can be improved by using acetoacetyl group containing polyvinyl alcohol.
水性エポキシ化合物(c)は突板の干割れ防止を目的として添加される。水性エポキシ化合物は、エチレングリコール、プロピレングリコール、グリセリンなどの多価アルコールをグリシジルエーテル化した化合物である。なお、前記多価アルコールの全てのアルコール基がグリシジルエーテル化されている必要はない。水性エポキシ化合物の好ましい添加量は、(a)酢酸ビニル樹脂エマルジョン100重量部に対して5〜30重量部である。 The aqueous epoxy compound (c) is added for the purpose of preventing dry cracking of the veneer. The aqueous epoxy compound is a compound obtained by glycidyl etherification of a polyhydric alcohol such as ethylene glycol, propylene glycol, or glycerin. Note that it is not necessary that all alcohol groups of the polyhydric alcohol are glycidyl etherified. A preferable addition amount of the aqueous epoxy compound is 5 to 30 parts by weight with respect to 100 parts by weight of (a) the vinyl acetate resin emulsion.
イソシアネート化合物(d)の添加により耐水性を向上させることができるため、例えば1類浸せきはく離試験に合格する程度の耐水性が必要とされる場合はイソシアネート化合物を添加することが好ましい。イソシアネート化合物の具体例として、2,4’−ジフェニルメタンジイソシアネート(2,4’−MDI)、4,4’−ジフェニルメタンジイソシアネート(4,4’−MDI)、トリレンジイソシアネート、ナフタレンジイソシアネート等の芳香族イソシアネート類、ヘキサメチレンジイソシアネート、イソホロンジイソシアネート等の脂肪族ポリイソシアネート類等が挙げられる。前記酢酸ビニル系樹脂エマルジョン(a)の固形分100重量部に対し、イソシアネート化合物を1重量部以上用いることで耐水性の顕著な向上が見られる。一方、30重量部以上用いても耐水性は頭打ちとなり、混合後の増粘が速くなるため作業性が低下する。 Since the water resistance can be improved by adding the isocyanate compound (d), it is preferable to add an isocyanate compound, for example, when the water resistance is required to pass the type 1 immersion peel test. Specific examples of the isocyanate compound include aromatic isocyanates such as 2,4′-diphenylmethane diisocyanate (2,4′-MDI), 4,4′-diphenylmethane diisocyanate (4,4′-MDI), tolylene diisocyanate, and naphthalene diisocyanate. And aliphatic polyisocyanates such as hexamethylene diisocyanate and isophorone diisocyanate. By using 1 part by weight or more of the isocyanate compound with respect to 100 parts by weight of the solid content of the vinyl acetate resin emulsion (a), the water resistance is remarkably improved. On the other hand, even if it is used in an amount of 30 parts by weight or more, the water resistance reaches a peak, and the viscosity increases after mixing, so workability decreases.
本発明の接着剤組成物は前記各成分の他、公知の添加剤を用いることができる。例えば、増粘剤、充填材、pH調整剤、粘着付与樹脂、界面活性剤、防腐剤、消泡剤、防錆剤等が挙げられる。 In the adhesive composition of the present invention, known additives can be used in addition to the above components. For example, a thickener, a filler, a pH adjuster, a tackifier resin, a surfactant, an antiseptic, an antifoaming agent, an antirust agent, and the like can be given.
以下、実施例に基づいて本発明をより具体的に説明するが、本発明は実施例に制限されるものではない。 EXAMPLES Hereinafter, although this invention is demonstrated more concretely based on an Example, this invention is not restrict | limited to an Example.
アセトアセチル基含有ポリビニルアルコールであるゴーセファイマーZ−320(日本合成化学工業株式会社製、商品名)10重量部を水90重量部に分散させ、90℃で3時間加熱攪拌した後冷却し、重亜硫酸ソーダ0.1部を混合することにより、AA化PVA水溶液(1)を得た。 10 parts by weight of Goosephimer Z-320 (trade name, manufactured by Nippon Synthetic Chemical Industry Co., Ltd.), which is an acetoacetyl group-containing polyvinyl alcohol, is dispersed in 90 parts by weight of water, heated and stirred at 90 ° C. for 3 hours, and then cooled. AA-PVA aqueous solution (1) was obtained by mixing 0.1 part of sodium bisulfite.
エチレン−酢酸ビニル共重合樹脂エマルジョンであるAE−156(アイカ工業株式会社製)60重量部、前記AA化PVA水溶液(1)20重量部、小麦粉15重量部、イソシアネート化合物であるAUH−1(アイカ工業株式会社製)1重量部、水性エポキシ化合物であるグリセリンポリグリシジルエーテル7重量部を混合し、実施例1の接着剤組成物を得た。 60 parts by weight of AE-156 (manufactured by Aika Kogyo Co., Ltd.) which is an ethylene-vinyl acetate copolymer resin emulsion, 20 parts by weight of the AA-PVA aqueous solution (1), 15 parts by weight of flour, and AUH-1 (Aika) which is an isocyanate compound 1 part by weight manufactured by Kogyo Co., Ltd. and 7 parts by weight of glycerin polyglycidyl ether which is an aqueous epoxy compound were mixed to obtain an adhesive composition of Example 1.
表1記載の配合にて実施例1と同様に実施例、比較例の各接着剤組成物を調製した。 Each adhesive composition of Examples and Comparative Examples was prepared in the same manner as in Example 1 with the formulation shown in Table 1.
各接着剤組成物をJAS1類合板(12mm厚、F☆☆☆☆)に100g/m2となるよう塗布し、メープルの突板(0.25mm厚)を貼り合わせ、105℃、0.7MPaで60秒間圧締して突板化粧合板を作製した。各突板化粧合板について1類浸せきはく離試験および2類浸せきはく離試験を行い、規格に適合したものを○、適合しなかったものを×と評価した。また、各突板化粧合板の突板の状態を確認し、顕著な割れがないものを○、顕著な割れが目立つものを×と評価した。 Each adhesive composition was applied to JAS1 plywood (12 mm thick, F ☆☆☆☆) at 100 g / m 2, and a maple veneer (0.25 mm thick) was bonded together at 105 ° C. and 0.7 MPa. A veneer plywood was prepared by pressing for 60 seconds. Each veneer plywood was subjected to a type 1 immersion peel test and a type 2 immersion peel test, and the case of conforming to the standard was evaluated as ◯, and the case of not conforming was evaluated as ×. Moreover, the state of the veneer of each veneer decorative plywood was confirmed, and the case where there was no remarkable crack was evaluated as ○, and the case where the significant crack was conspicuous was evaluated as ×.
実施例の各接着剤組成物を用いた場合、得られた突板化粧合板には顕著な割れがなかった。また、実施例1、2のようにイソシアネート化合物を用いることによって、高度の耐水性を得ることができる。一方、比較例の各接着剤組成物を用いた場合は顕著な割れが目つ結果であり、イソシアネート化合物を用いたことによって耐水性に優れる比較例2においても割れが発生していた。したがって、耐水性と割れの評価は必ずしも一致しないことが分かる。 When each adhesive composition of an Example was used, there was no remarkable crack in the obtained veneer decorative plywood. Moreover, high water resistance can be obtained by using an isocyanate compound like Example 1,2. On the other hand, when each adhesive composition of a comparative example was used, the remarkable crack was a result, and the crack also generate | occur | produced also in the comparative example 2 which is excellent in water resistance by using an isocyanate compound. Therefore, it turns out that water resistance and the evaluation of a crack do not necessarily correspond.
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| JP2008089256A JP2009242512A (en) | 2008-03-31 | 2008-03-31 | Adhesive composition |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010229307A (en) * | 2009-03-27 | 2010-10-14 | Aica Kogyo Co Ltd | Method for producing adhesive composition and veneer decorative material |
Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS555937A (en) * | 1978-06-27 | 1980-01-17 | Koyo Sangyo Kk | Adhesive composition |
| JPS58217571A (en) * | 1982-06-11 | 1983-12-17 | Nippon Synthetic Chem Ind Co Ltd:The | emulsion composition |
| JPS591581A (en) * | 1982-06-28 | 1984-01-06 | Nippon Synthetic Chem Ind Co Ltd:The | wood adhesive composition |
| JPS60240777A (en) * | 1984-05-15 | 1985-11-29 | Aica Kogyo Co Ltd | Two-pack, water-dispersed adhesive |
| JPH04255785A (en) * | 1991-02-06 | 1992-09-10 | Aica Kogyo Co Ltd | Two-pack type composition adhesive |
| JPH05117618A (en) * | 1991-04-01 | 1993-05-14 | Nippon Shokubai Co Ltd | Two-pack, water-based adhesive composition |
| JPH09188862A (en) * | 1996-01-08 | 1997-07-22 | Sumitomo Chem Co Ltd | Aqueous emulsion adhesive |
| JPH09249865A (en) * | 1996-03-18 | 1997-09-22 | Sekisui Chem Co Ltd | Adhesive composition and paper tube using the same |
| JPH10219219A (en) * | 1997-02-05 | 1998-08-18 | Kuraray Co Ltd | Water-based adhesive |
| JP2004197049A (en) * | 2002-12-20 | 2004-07-15 | Nippon Nsc Ltd | Water-base adhesive |
| JP2006290928A (en) * | 2005-04-06 | 2006-10-26 | Aica Kogyo Co Ltd | Adhesive composition |
| JP2007246828A (en) * | 2006-03-17 | 2007-09-27 | Aica Kogyo Co Ltd | Adhesive composition and adhesive agent for woodworking comprising the same |
-
2008
- 2008-03-31 JP JP2008089256A patent/JP2009242512A/en active Pending
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS555937A (en) * | 1978-06-27 | 1980-01-17 | Koyo Sangyo Kk | Adhesive composition |
| JPS58217571A (en) * | 1982-06-11 | 1983-12-17 | Nippon Synthetic Chem Ind Co Ltd:The | emulsion composition |
| JPS591581A (en) * | 1982-06-28 | 1984-01-06 | Nippon Synthetic Chem Ind Co Ltd:The | wood adhesive composition |
| JPS60240777A (en) * | 1984-05-15 | 1985-11-29 | Aica Kogyo Co Ltd | Two-pack, water-dispersed adhesive |
| JPH04255785A (en) * | 1991-02-06 | 1992-09-10 | Aica Kogyo Co Ltd | Two-pack type composition adhesive |
| JPH05117618A (en) * | 1991-04-01 | 1993-05-14 | Nippon Shokubai Co Ltd | Two-pack, water-based adhesive composition |
| JPH09188862A (en) * | 1996-01-08 | 1997-07-22 | Sumitomo Chem Co Ltd | Aqueous emulsion adhesive |
| JPH09249865A (en) * | 1996-03-18 | 1997-09-22 | Sekisui Chem Co Ltd | Adhesive composition and paper tube using the same |
| JPH10219219A (en) * | 1997-02-05 | 1998-08-18 | Kuraray Co Ltd | Water-based adhesive |
| JP2004197049A (en) * | 2002-12-20 | 2004-07-15 | Nippon Nsc Ltd | Water-base adhesive |
| JP2006290928A (en) * | 2005-04-06 | 2006-10-26 | Aica Kogyo Co Ltd | Adhesive composition |
| JP2007246828A (en) * | 2006-03-17 | 2007-09-27 | Aica Kogyo Co Ltd | Adhesive composition and adhesive agent for woodworking comprising the same |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010229307A (en) * | 2009-03-27 | 2010-10-14 | Aica Kogyo Co Ltd | Method for producing adhesive composition and veneer decorative material |
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