JP6872801B2 - Highly moisture-proof adhesive composition - Google Patents
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- JP6872801B2 JP6872801B2 JP2018051913A JP2018051913A JP6872801B2 JP 6872801 B2 JP6872801 B2 JP 6872801B2 JP 2018051913 A JP2018051913 A JP 2018051913A JP 2018051913 A JP2018051913 A JP 2018051913A JP 6872801 B2 JP6872801 B2 JP 6872801B2
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Description
本発明は、高防湿性接着剤組成物に関する。 The present invention relates to a highly moisture-proof adhesive composition.
従来、住宅のドア等の内装部材として、木質材料からなる枠体の両面に面材を接着したサンドイッチ構造を有するフラッシュパネルが用いられている。前記フラッシュパネルでは、高い防湿性能が必要とされる場合には、前記ドアの内部となる前記面材の裏面に防湿フィルムを接着することが行われている。ところが、このようにする場合には、前記面材の裏面に防湿フィルムを接着した後、該防湿フィルムに前記枠材を接着するという2つの製造工程が必要になる。 Conventionally, as an interior member of a door or the like of a house, a flash panel having a sandwich structure in which face materials are bonded to both sides of a frame made of wood material has been used. In the flash panel, when high moisture-proof performance is required, a moisture-proof film is adhered to the back surface of the face material which is the inside of the door. However, in this case, two manufacturing steps are required: after adhering the moisture-proof film to the back surface of the face material, and then adhering the frame material to the moisture-proof film.
一方、住宅等の内装部材に塗布して防湿性を付与する塗料として、塩化ビニリデン樹脂を含む防湿塗料組成物が知られている(例えば、特許文献1参照)。前記ビニリデン樹脂は結晶性が高いので、前記防湿塗料組成物の被膜によれば前記内装部材に優れた防湿性を付与することができる。 On the other hand, a moisture-proof coating composition containing a vinylidene chloride resin is known as a coating material that is applied to an interior member of a house or the like to impart moisture resistance (see, for example, Patent Document 1). Since the vinylidene resin has high crystallinity, the coating of the moisture-proof coating composition can impart excellent moisture-proof properties to the interior member.
前記フラッシュパネルにおいて、製造工程を簡略化するために、前記防湿フィルムに代えて前記塩化ビニリデン樹脂を含む建材用防湿塗料組成物を塗布して被膜を形成し、該被膜を接着剤として前記枠体を接着できれば好都合である。 In the flash panel, in order to simplify the manufacturing process, a moisture-proof coating composition for building materials containing the vinylidene chloride resin is applied instead of the moisture-proof film to form a film, and the film is used as an adhesive to form the frame. It would be convenient if they could be glued together.
しかしながら、前記塩化ビニリデン樹脂は接着剤として用いた場合、十分な接着性能を得ることができないという不都合がある。 However, when the vinylidene chloride resin is used as an adhesive, there is a disadvantage that sufficient adhesive performance cannot be obtained.
本発明は、かかる不都合を解消して、その被膜により塗布対象物に優れた防湿性を付与することができる一方、優れた接着性能を備える高防湿性接着剤組成物を提供することを目的とする。 An object of the present invention is to provide a highly moisture-proof adhesive composition having excellent adhesive performance while eliminating such inconveniences and imparting excellent moisture-proof properties to the object to be coated by the coating film. To do.
本発明者らは、塩化ビニリデン樹脂を含む防湿性塗料組成物を接着剤としたときに、十分な接着性能を得ることができない理由について、鋭意検討した。その結果、塩化ビニリデン樹脂の優れた結晶性が接着性能を阻害しており、結晶性を調整することにより優れた接着性能が得られることを見出し、本発明に到達した。 The present inventors have diligently investigated the reason why sufficient adhesive performance cannot be obtained when a moisture-proof coating composition containing a vinylidene chloride resin is used as an adhesive. As a result, it was found that the excellent crystallinity of the vinylidene chloride resin hinders the adhesive performance, and that the excellent crystallinity can be obtained by adjusting the crystallinity, and the present invention has been reached.
そこで、本発明の高防湿性接着剤組成物は、前記目的を達成するために、塩化ビニリデン樹脂を含むエマルジョンと、塩化ビニリデン樹脂の結晶化を阻害する結晶化阻害剤とを含む高防湿性接着剤組成物であって、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、前記結晶化阻害剤を1〜10質量部の範囲で含むことを特徴とする。 Accordingly, high moisture resistance adhesive composition of the present invention, in order to achieve the object, the emulsion containing vinylidene chloride resin, high moisture resistance adhesive comprising a crystallization inhibitor which inhibits crystallization of vinylidene chloride resin The agent composition is characterized by containing the crystallization inhibitor in the range of 1 to 10 parts by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin.
高防湿性接着剤組成物は、塩化ビニリデン樹脂を含むので、塗布対象物に塗布されたときにその乾燥被膜により優れた防湿性を付与することができる一方、前記結晶化阻害剤により塩化ビニリデン樹脂の結晶化を調整して優れた接着性能を得ることができる。 Since the highly moisture-proof adhesive composition contains a vinylidene chloride resin, it is possible to impart excellent moisture-proof properties to the dry film when it is applied to the object to be coated, while the vinylidene chloride resin is provided by the crystallization inhibitor. The crystallization of the resin can be adjusted to obtain excellent adhesive performance.
本発明の高防湿性接着剤組成物は、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、前記結晶化阻害剤の含有量が1質量部未満であるときには、該塩化ビニリデン樹脂の結晶性が過大になり、十分な接着性能を得ることができない。また、本発明の高防湿性接着剤組成物は、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、前記結晶化阻害剤の含有量が10質量部を超えるときには、該塩化ビニリデン樹脂の結晶性が過小になり、塗布対象物に十分な防湿性を付与できない。 In the highly moisture-proof adhesive composition of the present invention, when the content of the crystallization inhibitor is less than 1 part by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin, the crystallinity of the vinylidene chloride resin is high. It becomes excessive, sufficient adhesion performance that can not be be obtained. Further, in the highly moisture-proof adhesive composition of the present invention, when the content of the crystallization inhibitor exceeds 10 parts by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin, the crystallization of the vinylidene chloride resin is obtained. becomes too small, that can not be provided with sufficient moisture resistance to the object to be coated.
本発明の高防湿性接着剤組成物において、前記結晶化阻害剤としては、例えば、安息香酸エステル系可塑剤、アクリル系可塑剤、アジピン酸エーテル系可塑剤、コハク酸ジメチル、アジピン酸ジメチル、グルタル酸ジメチル、ジブチルジグリコール、ブチルカルビトールアセテートからなる群から選択される1種の化合物を用いることができる。 In the highly moisture-proof adhesive composition of the present invention, examples of the crystallization inhibitor include benzoic acid ester-based plasticizers, acrylic-based plasticizers, adipate ether-based plasticizers, dimethyl succinate, dimethyl adipate, and glutaric acid. One compound selected from the group consisting of dimethyl acid acid, dibutyl diglycol, and butyl carbitol acetate can be used.
本発明の高防湿性接着剤組成物は、さらに、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、粘性調整剤を0.1〜10質量部の範囲で含むことが好ましい。本発明の高防湿性接着剤組成物は、前記粘性調整剤を含むことにより、作業時の塗工性を上げるという効果を得ることができる。本発明の高防湿性接着剤組成物は、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、前記粘性調整剤の含有量が0.1質量部未満であるときには、塩化ビニリデン樹脂を含むエマルジョンの粘度が上がらず、塗工性を改善することができないことがある。また、本発明の高防湿性接着剤組成物は、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、前記粘性調整剤の含有量が10質量部を超えるときには、エマルジョンのショックが発生し、うまく混合することができないことがある。 The highly moisture-proof adhesive composition of the present invention further preferably contains a viscosity modifier in the range of 0.1 to 10 parts by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin. The highly moisture-proof adhesive composition of the present invention can have the effect of improving the coatability during work by containing the viscosity modifier. The highly moisture-proof adhesive composition of the present invention is an emulsion containing a vinylidene chloride resin when the content of the viscosity modifier is less than 0.1 parts by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin. The viscosity may not increase and the coatability may not be improved. Further, in the highly moisture-proof adhesive composition of the present invention, when the content of the viscosity modifier exceeds 10 parts by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin, a shock of the emulsion occurs, and the emulsion is successfully shocked. It may not be possible to mix.
本発明の高防湿性接着剤組成物において、前記粘性調整剤としては、例えば、アクリル系粘性調整剤、ウレタン系粘性調整剤、ヒドロキシメチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロース、カルボキシメチルセルロース、キサンタンガム、ダイユータンガム、グアーガム、ポリアクリル酸ナトリウム、二酸化ケイ素からなる群から選択される1種の化合物を用いることができる。 In the highly moisture-proof adhesive composition of the present invention, examples of the viscosity adjusting agent include acrylic viscosity adjusting agents, urethane viscosity adjusting agents, hydroxymethyl celluloses, hydroxyethyl celluloses, hydroxypropyl methyl celluloses, carboxymethyl celluloses, xanthan gums, and Daiyutan. One compound selected from the group consisting of gum, guar gum, sodium polyacrylate, and silicon dioxide can be used.
次に、本発明の実施の形態についてさらに詳しく説明する。 Next, embodiments of the present invention will be described in more detail.
本実施形態の高防湿性接着剤組成物は、塩化ビニリデン樹脂を含むエマルジョンと、塩化ビニリデン樹脂の結晶化を阻害する結晶化阻害剤とを含み、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、前記結晶化阻害剤を1〜10質量部の範囲で含む。 The highly moisture-proof adhesive composition of the present embodiment contains an emulsion containing a vinylidene chloride resin and a crystallization inhibitor that inhibits the crystallization of the vinylidene chloride resin, with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin. , including the crystallization inhibitor in the range of 1 to 10 parts by weight.
前記塩化ビニリデン樹脂を含むエマルジョンは、塩化ビニリデン単量体の単独重合物を含むエマルジョンであってもよく、塩化ビニリデン単量体と、これと共重合可能な1種以上の他の単量体との共重合体のエマルジョンであってもよい。塩化ビニリデン共重合体ラテックスとしては、例えば、旭化成株式会社製、サランラテックス(登録商標)の各グレード品を用いることができる。 The emulsion containing the vinylidene chloride resin may be an emulsion containing a homopolymer of the vinylidene chloride monomer, and the vinylidene chloride monomer and one or more other monomers copolymerizable therewith may be used. It may be an emulsion of the copolymer of. As the vinylidene chloride copolymer latex, for example, each grade product of Saran Latex (registered trademark) manufactured by Asahi Kasei Corporation can be used.
また、前記結晶化阻害剤としては、例えば、安息香酸エステル系可塑剤、アクリル系可塑剤、アジピン酸エーテル系可塑剤、コハク酸ジメチル、アジピン酸ジメチル、グルタル酸ジメチル、ジブチルジグリコール、ブチルカルビトールアセテートからなる群から選択される1種の化合物を用いることができる。前記結晶化阻害剤は、TVOCを発生させる可能性があることから、沸点200℃以上の化合物であることがさらに好ましい。 Examples of the crystallization inhibitor include benzoic acid ester-based plasticizers, acrylic-based plasticizers, adipate ether-based plasticizers, dimethyl succinate, dimethyl adipate, dimethyl glutarate, dibutyl diglycol, and butyl carbitol. One compound selected from the group consisting of acetates can be used. The crystallization inhibitor is more preferably a compound having a boiling point of 200 ° C. or higher because it may generate TVOC.
また、本実施形態の高防湿性接着剤組成物は、さらに、前記塩化ビニリデン樹脂を含むエマルジョン100質量部に対し、粘性調整剤を0.1〜10質量部の範囲で含むことが好ましい。前記粘性調整剤としては、例えば、アクリル系粘性調整剤、ウレタン系粘性調整剤、ヒドロキシメチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロース、カルボキシメチルセルロース、キサンタンガム、ダイユータンガム、グアーガム、ポリアクリル酸ナトリウム、二酸化ケイ素からなる群から選択される1種の化合物を用いることができる。 Further, the highly moisture-proof adhesive composition of the present embodiment preferably further contains a viscosity modifier in the range of 0.1 to 10 parts by mass with respect to 100 parts by mass of the emulsion containing the vinylidene chloride resin. Examples of the viscosity adjusting agent include acrylic viscosity adjusting agents, urethane viscosity adjusting agents, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose, carboxymethyl cellulose, xanthan gum, Daiyutan gum, guar gum, sodium polyacrylate, and silicon dioxide. One compound selected from the group can be used.
本実施形態の高防湿性接着剤組成物は、住宅のドア、壁等の高い防湿性を必要とする内装材料等を塗布対象物として、該塗布対象物に優れた防湿性を付与する一方、その優れた接着性能により、該塗布対象物を他の被着材に接着する用途等に好適に用いることができる。このような用途として、例えば、フラッシュパネルの一方の面材を塗布対象物とし、該面材に枠体を接着する用途等を挙げることができる。 The highly moisture-proof adhesive composition of the present embodiment is applied to an interior material or the like that requires high moisture-proof properties such as a door or a wall of a house, and imparts excellent moisture-proof properties to the coated object. Due to its excellent adhesive performance, it can be suitably used for applications such as adhering the object to be coated to another adherend. Examples of such an application include an application in which one face material of a flash panel is used as an object to be coated and a frame body is adhered to the face material.
次に、本発明の実施例及び比較例を示す。 Next, Examples and Comparative Examples of the present invention will be shown.
〔実施例1〕
本実施例では、まず、ガラス製フラスコに塩化ビニリデン共重合ラテックス(旭化成株式会社製、商品名:サランラテックス L502、固形分50質量%)を93質量部取り、ステンレス製の撹拌羽で撹拌しながら、粘性調整剤(株式会社ADEKA製、商品名:アデカノール UH−420、固形分30質量%)2質量部と、結晶化阻害剤としてのジブチルジグリコール(日本乳化剤株式会社製)5質量部とを添加して、高防湿性接着剤組成物を得た。
[Example 1]
In this embodiment, first, 93 parts by mass of vinylidene chloride copolymer latex (manufactured by Asahi Kasei Co., Ltd., trade name: Saran latex L502, solid content 50% by mass) is taken in a glass flask, and the mixture is stirred with a stainless steel stirring blade. , 2 parts by mass of viscosity modifier (manufactured by ADEKA Co., Ltd., trade name: Adecanol UH-420, solid content 30% by mass) and 5 parts by mass of dibutyldiglycol as a crystallization inhibitor (manufactured by Nippon Emulsifier Co., Ltd.) Addition gave a highly moisture-proof adhesive composition.
次に、本実施例で得られた高防湿性接着剤組成物について、最低造膜温度、透湿抵抗、接着強さ、材料破断率をそれぞれ次のようにして測定した。結果を表1に示す。 Next, with respect to the highly moisture-proof adhesive composition obtained in this example, the minimum film-forming temperature, moisture permeation resistance, adhesive strength, and material breaking rate were measured as follows. The results are shown in Table 1.
〔最低造膜温度〕
本実施例で得られた高防湿性接着剤組成物を、各温度環境下で平滑なアルミニウム箔上にフィルムアプリケーターを用いて100μmの厚さに塗布し、透明な膜を形成する温度と膜を形成しない温度との境界を測定し、透明な膜を形成する温度を最低造膜温度とする。
[Minimum film formation temperature]
The highly moisture-proof adhesive composition obtained in this example is applied to a thickness of 100 μm on a smooth aluminum foil under each temperature environment using a film applicator, and the temperature and film for forming a transparent film are adjusted. The boundary with the temperature at which the film is not formed is measured, and the temperature at which the transparent film is formed is defined as the minimum film formation temperature.
〔透湿抵抗〕
JIS A 1324「建築材料の透湿性測定方法」5.2カップ法に基づいて測定する。
[Moisture permeation resistance]
Measured based on JIS A 1324 "Method for measuring moisture permeability of building materials" 5.2 cup method.
まず、本実施例で得られた高防湿性接着剤組成物を、ボード紙に接着剤を200g/m2の量で塗布し、2日間養生したものを試料とする。次に、前記試料の表面に予め透湿させる範囲がわかるように印を付け、吸湿剤として所定量の塩化カルシウムを収容した透湿カップに前記試料を取り付ける。 First, the highly moisture-proof adhesive composition obtained in this example is applied to a board paper at an amount of 200 g / m 2 and cured for 2 days as a sample. Next, the surface of the sample is marked in advance so that the range of moisture permeation can be seen, and the sample is attached to a moisture permeation cup containing a predetermined amount of calcium chloride as a hygroscopic agent.
前記透湿カップは、250mm角、深さ30mmの内寸を備える下部に、300mm角、深さ30mmの内寸を備える上部が連設され、下部と上部との間に段差部が形成されている。前記吸湿剤は前記透湿カップの下部に収容されており、前記試料は前記段差部に取り付けられる。 In the moisture permeable cup, an upper portion having an inner dimension of 300 mm square and a depth of 30 mm is continuously provided in a lower portion having an inner dimension of 250 mm square and a depth of 30 mm, and a step portion is formed between the lower portion and the upper portion. There is. The hygroscopic agent is housed in the lower part of the moisture permeable cup, and the sample is attached to the step portion.
次に、前記透湿カップに取り付けられた前記試料の周囲をアルミニウムテープでシールする一方、該試料の透湿させる範囲以外の部分をパラフィンワックスでシールし、透湿させる範囲以外からの透湿が生じないようにする。 Next, while the periphery of the sample attached to the moisture permeable cup is sealed with aluminum tape, the portion of the sample other than the moisture permeable range is sealed with paraffin wax, and moisture permeable from the range other than the moisture permeable range. Prevent it from occurring.
次に、前記透湿カップを、23℃、相対湿度50%の環境の恒温恒湿槽内に静置し、所定の時間間隔毎に質量を測定し、その質量変化から次式に従って透湿抵抗(m2sPa/ng)を求める。 Next, the moisture permeable cup is allowed to stand in a constant temperature and humidity chamber in an environment of 23 ° C. and a relative humidity of 50%, the mass is measured at predetermined time intervals, and the moisture permeability resistance is measured according to the following formula from the mass change. ( M 2 spa / ng) is calculated.
透湿抵抗(m2sPa/ng)=(P1−P2)×A/G
P1:恒温恒湿槽内の空気の水蒸気圧(1405.5Pa、23℃、相対湿度50%の環境の水蒸気圧)
P2:透湿カップ内の空気の水蒸気圧(0Pa)
A:透湿面積(透湿させる範囲の面積、m2)
G:測定時間毎の質量の増加量(ng/s)
〔接着強さ、材料破断率〕
本実施例で得られた高防湿性接着剤組成物を、ラワン合板と合板裏打ちしたMDF(中密度繊維板)との接着面に200g/m2の塗布量(乾燥前の塗布量)で塗布し、20℃の環境下、圧締圧力0.01MPa、圧締時間1時間の条件で接着し、試験面積40mm×40mm、試験速度3.0mmの条件で平面引張り試験を行い、接着強さと材料破断率とを求めた。
Moisture permeation resistance (m 2 spa / ng) = (P 1 − P 2 ) × A / G
P 1 : Water vapor pressure of air in a constant temperature and humidity chamber (1405.5 Pa, 23 ° C, water vapor pressure in an environment with a relative humidity of 50%)
P 2 : Water vapor pressure of air in the moisture permeable cup (0 Pa)
A: Moisture permeable area (area of moisture permeable range, m 2 )
G: Mass increase per measurement time (ng / s)
[Adhesive strength, material breakage rate]
The highly moisture-proof adhesive composition obtained in this example is applied to the adhesive surface between Lauan plywood and MDF (medium density fiberboard) lined with plywood at a coating amount of 200 g / m 2 (application amount before drying). Then, in an environment of 20 ° C., bonding was performed under the conditions of a pressing pressure of 0.01 MPa and a pressing time of 1 hour, and a plane tensile test was conducted under the conditions of a test area of 40 mm × 40 mm and a test speed of 3.0 mm. The break rate was calculated.
〔実施例2〕
本実施例では、塩化ビニリデン共重合ラテックス(旭化成株式会社製、商品名:サランラテックス L502、固形分50質量%)を90質量部、粘性調整剤(株式会社ADEKA製、商品名:アデカノール UH−420、固形分30質量%)を5質量部、結晶化阻害剤としてのジブチルジグリコール(日本乳化剤株式会社製)を5質量部とした以外は、実施例1と全く同一にして高防湿性接着剤組成物を得た。
[Example 2]
In this example, 90 parts by mass of vinylidene chloride copolymer latex (manufactured by Asahi Kasei Co., Ltd., trade name: Saran latex L502, solid content 50% by mass), viscosity modifier (manufactured by ADEKA Co., Ltd., trade name: Adecanol UH-420) , Solid content 30% by mass) was 5 parts by mass, and dibutyldiglycol as a crystallization inhibitor (manufactured by Nippon Emulsifier Co., Ltd.) was 5 parts by mass. The composition was obtained.
次に、本実施例で得られた高防湿性接着剤組成物について、最低造膜温度、透湿抵抗、接着強さ、材料破断率を、実施例1と全く同一にして測定した。結果を表1に示す。 Next, with respect to the highly moisture-proof adhesive composition obtained in this example, the minimum film-forming temperature, moisture permeation resistance, adhesive strength, and material breaking rate were measured in exactly the same manner as in Example 1. The results are shown in Table 1.
〔比較例1〕
本比較例では、塩化ビニリデン共重合ラテックス(旭化成株式会社製、商品名:サランラテックス L502、固形分50質量%)のみを接着剤組成物とした。
[Comparative Example 1]
In this comparative example, only vinylidene chloride copolymer latex (manufactured by Asahi Kasei Corporation, trade name: Saran Latex L502, solid content 50% by mass) was used as the adhesive composition.
次に、本比較例の接着剤組成物について、最低造膜温度、透湿抵抗、接着強さ、材料破断率を、実施例1と全く同一にして測定した。結果を表1に示す。 Next, for the adhesive composition of this comparative example, the minimum film forming temperature, moisture permeation resistance, adhesive strength, and material breaking rate were measured in exactly the same manner as in Example 1. The results are shown in Table 1.
〔比較例2〕
本比較例では、塩化ビニリデン共重合ラテックス(旭化成株式会社製、商品名:サランラテックス L502、固形分50質量%)を95質量部、粘性調整剤(株式会社ADEKA製、商品名:アデカノール UH−420、固形分30質量%)を5質量部とし、結晶化阻害剤を全く用いなかった以外は、実施例1と全く同一にして接着剤組成物を得た。
[Comparative Example 2]
In this comparative example, 95 parts by mass of vinylidene chloride copolymer latex (manufactured by Asahi Kasei Co., Ltd., trade name: Saran latex L502, solid content 50% by mass), viscosity modifier (manufactured by ADEKA Co., Ltd., trade name: Adecanol UH-420) , Solid content 30% by mass), and the same as in Example 1 except that no crystallization inhibitor was used to obtain an adhesive composition.
次に、本比較例で得られた接着剤組成物について、最低造膜温度、透湿抵抗、接着強さ、材料破断率を、実施例1と全く同一にして測定した。結果を表1に示す。 Next, with respect to the adhesive composition obtained in this comparative example, the minimum film forming temperature, moisture permeation resistance, adhesive strength, and material breaking rate were measured in exactly the same manner as in Example 1. The results are shown in Table 1.
表1から、塩化ビニリデン樹脂を含むエマルジョン(塩化ビニリデン共重合ラテックス)と、塩化ビニリデン樹脂の結晶化を阻害する結晶化阻害剤としてのジブチルジグリコールとを含む実施例1、2の高防湿性接着剤組成物によれば、最低造膜温度が5℃と低く、接着強さ及び材料破断率が大きく優れた接着性能を備える上、透湿抵抗も高く、塗布対象物に優れた防湿性を付与することができることが明らかである。 From Table 1, the highly moisture-proof adhesion of Examples 1 and 2 containing an emulsion containing a vinylidene chloride resin (vinylidene chloride copolymer latex) and dibutyldiglycol as a crystallization inhibitor that inhibits the crystallization of the vinylidene chloride resin. According to the agent composition, the minimum film-forming temperature is as low as 5 ° C., the adhesive strength and the material breaking rate are large, the adhesive performance is excellent, the moisture permeation resistance is high, and the object to be coated is provided with excellent moisture resistance. It is clear that it can be done.
一方、塩化ビニリデン樹脂を含むエマルジョン(塩化ビニリデン共重合ラテックス)のみからなるか、塩化ビニリデン樹脂を含むエマルジョン(塩化ビニリデン共重合ラテックス)と粘性調整剤とを含み、前記結晶化阻害剤を含まない比較例1、2の接着剤組成物によれば、透湿抵抗は実施例1、2よりも高いものの、最低造膜温度が23℃と高く、接着強さ及び材料破断率が小さく実質的に接着性能を備えていないことが明らかである。 On the other hand, a comparison consisting only of an emulsion containing a vinylidene chloride resin (vinylidene chloride copolymerized latex) or containing an emulsion containing a vinylidene chloride resin (vinylidene chloride copolymerized latex) and a viscosity modifier and not containing the crystallization inhibitor. According to the adhesive compositions of Examples 1 and 2, the moisture permeation resistance is higher than that of Examples 1 and 2, but the minimum film-forming temperature is as high as 23 ° C. It is clear that it does not have the performance.
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