JP2003336021A - Tackifier resin emulsion and aqueous adhesive composition - Google Patents

Tackifier resin emulsion and aqueous adhesive composition

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Publication number
JP2003336021A
JP2003336021A JP2002146537A JP2002146537A JP2003336021A JP 2003336021 A JP2003336021 A JP 2003336021A JP 2002146537 A JP2002146537 A JP 2002146537A JP 2002146537 A JP2002146537 A JP 2002146537A JP 2003336021 A JP2003336021 A JP 2003336021A
Authority
JP
Japan
Prior art keywords
emulsion
tackifying resin
resin emulsion
parts
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2002146537A
Other languages
Japanese (ja)
Other versions
JP3925302B2 (en
Inventor
Yoshinori Takagi
芳徳 高木
Yosuke Tsushima
洋介 津島
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arakawa Chemical Industries Ltd
Original Assignee
Arakawa Chemical Industries Ltd
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Filing date
Publication date
Application filed by Arakawa Chemical Industries Ltd filed Critical Arakawa Chemical Industries Ltd
Priority to JP2002146537A priority Critical patent/JP3925302B2/en
Publication of JP2003336021A publication Critical patent/JP2003336021A/en
Application granted granted Critical
Publication of JP3925302B2 publication Critical patent/JP3925302B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

<P>PROBLEM TO BE SOLVED: To provide a tackifier resin emulsion excellent in emulsifying properties of the emulsion and storage stability, and an aqueous adhesive composition excellent particularly in initial adhesive properties and applicability not to speak of self-adhesive characteristics under ordinary conditions. <P>SOLUTION: The tackifier resin emulsion comprises a tackifier resin, an emulsifier and water, where a tackifier resin composition having an acid value of 90-220 and a softening point of 80-160°C is employed as the tackifier resin. The aqueous adhesive composition comprises at least one base polymer selected from the group consisting of an acrylic polymer emulsion, a rubber-based latex and a synthetic resin-based emulsion, and the tackifier resin emulsion. <P>COPYRIGHT: (C)2004,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、粘着付与樹脂エマ
ルジョンおよび水系接着剤組成物に関する。詳しくは、
エマルジョンの乳化性、貯蔵安定性および通常の条件下
における接着特性を向上させ得る粘着付与樹脂エマルジ
ョンおよび当該粘着付与樹脂エマルジョンを用いた、特
に初期接着性や塗工性に優れた水系接着剤組成物に関す
る。
TECHNICAL FIELD The present invention relates to a tackifying resin emulsion and a water-based adhesive composition. For more information,
A tackifying resin emulsion capable of improving the emulsifying property of an emulsion, storage stability and adhesive properties under normal conditions, and a water-based adhesive composition using the tackifying resin emulsion, which is particularly excellent in initial adhesiveness and coatability. Regarding

【0002】[0002]

【従来の技術】接着剤は、包装、建築、建材などの幅広
い分野で利用されており、一般的にはアクリル系重合体
等のベースポリマーに、タック等の粘着特性を付与する
ために粘着付与樹脂が添加されている。接着剤は、従
来、溶剤型が汎用されてきたが、近年では、大気汚染が
ないこと、安全衛生に優れていることおよび省資源に適
すること等の種々の利点を有する水系エマルジョン型接
着剤に転換されつつある。
2. Description of the Related Art Adhesives are used in a wide range of fields such as packaging, construction, and building materials. Generally, a base polymer such as an acrylic polymer is tackified in order to impart tackiness and other adhesive properties. Resin has been added. Conventionally, solvent-based adhesives have been widely used, but in recent years, water-based emulsion adhesives that have various advantages such as no air pollution, excellent safety and hygiene, and suitable for resource saving. It is being converted.

【0003】従来、水系接着剤としては、アクリル系重
合体エマルジョン、スチレン−ブタジエン共重合体ラテ
ックス、天然ゴムラテックス、クロロプレンラテックス
等をベースポリマーとし、これにロジン類、ロジン誘導
体、石油系樹脂、テルペン系樹脂、フェノール樹脂、ケ
トン樹脂等の粘着付与樹脂エマルジョンを配合してなる
水系接着剤組成物が知られている。通常、かかる粘着付
与樹脂エマルジョンには、ベースポリマーとの相溶性
や、接着物性が良好であることから、ロジン類やロジン
誘導体等のロジン系樹脂のエマルジョンが広く使用され
ている。
Conventionally, as a water-based adhesive, an acrylic polymer emulsion, a styrene-butadiene copolymer latex, a natural rubber latex, a chloroprene latex and the like have been used as a base polymer, on which rosins, rosin derivatives, petroleum resins and terpenes are added. A water-based adhesive composition containing a tackifying resin emulsion such as a base resin, a phenol resin, or a ketone resin is known. Usually, emulsions of rosin-based resins such as rosins and rosin derivatives are widely used for such tackifying resin emulsions because they have good compatibility with the base polymer and good adhesive properties.

【0004】しかし、これらロジン系樹脂のエマルジョ
ンを使用した場合も、水系接着剤において特に必要とさ
れる初期接着性や塗工性が不十分であり、これらを向上
させ得る水系接着剤が求められている。
However, even when these emulsions of rosin-based resins are used, the initial adhesiveness and coatability required for water-based adhesives are insufficient, and water-based adhesives that can improve these properties are required. ing.

【0005】[0005]

【発明が解決しようとする課題】本発明は、エマルジョ
ンの乳化性、貯蔵安定性に優れた粘着付与樹脂エマルジ
ョンおよび通常の条件下における粘着特性が優れるのは
勿論のこと、特に初期接着性や塗工性に優れた水系接着
剤組成物を提供することを目的とする。
DISCLOSURE OF THE INVENTION The present invention is not only excellent in the emulsifying property of an emulsion and the storage stability but also in the tackifying resin emulsion under ordinary conditions, and particularly in the initial adhesiveness and the coating property. It is an object to provide a water-based adhesive composition having excellent workability.

【0006】[0006]

【課題を解決するための手段】本発明者らは、前記従来
技術の課題を解決すべく、粘着付与樹脂の組成面から鋭
意検討を重ねた結果、粘着付与樹脂として、特定の酸価
と軟化点を有する粘着付与樹脂組成物を用いた粘着付与
樹脂エマルジョンを用いることにより、初期接着性や塗
工性に優れた水系接着剤組成物が得られ、特に、不飽和
酸変性ロジン類を含有する粘着付与樹脂組成物を用いた
粘着付与樹脂エマルジョンを用いることにより初期接着
性や塗工性を向上させうることを見出した。本発明はか
かる新たな知見に基づいて完成されたものである。
Means for Solving the Problems The inventors of the present invention have made earnest studies from the viewpoint of the composition of the tackifying resin in order to solve the above-mentioned problems of the prior art. As a result, the tackifying resin has a specific acid value and a softening property. By using a tackifying resin emulsion using a tackifying resin composition having points, a water-based adhesive composition having excellent initial adhesiveness and coatability can be obtained, and particularly, an unsaturated acid-modified rosin is contained. It has been found that the use of a tackifying resin emulsion containing the tackifying resin composition can improve the initial adhesiveness and coatability. The present invention has been completed based on this new finding.

【0007】すなわち、本発明は、粘着付与樹脂、乳化
剤および水からなる粘着付与樹脂エマルジョンにおい
て、粘着付与樹脂として酸価が90〜220、かつ軟化
点が80〜160℃の粘着付与樹脂組成物を使用するこ
とを特徴とする粘着付与樹脂エマルジョン;アクリル系
重合体エマルジョン、ゴム系ラテックスおよび合成樹脂
系エマルジョンからなる群より選ばれる少なくとも一種
のベースポリマーと当該粘着付与樹脂エマルジョンとを
含有してなることを特徴とする水系接着剤組成物に関す
る。
That is, the present invention provides a tackifying resin emulsion consisting of a tackifying resin, an emulsifier and water, which is a tackifying resin composition having an acid value of 90 to 220 and a softening point of 80 to 160 ° C. A tackifying resin emulsion characterized by being used; comprising at least one base polymer selected from the group consisting of an acrylic polymer emulsion, a rubber latex and a synthetic resin emulsion, and the tackifying resin emulsion. And a water-based adhesive composition.

【0008】本発明で使用する粘着付与樹脂組成物とし
ては、酸価が90〜220、かつ軟化点が80〜160
℃となるものであれば、特に制限されず公知のものを使
用することができる。酸価が90に満たない場合は、塗
工性および粘着特性が低下し、220を超える場合は、
乳化時の安定性が低下し、かつ粘着特性が低下するため
好ましくない。また軟化点が80℃に満たない場合は、
粘着特性が低下し、160℃を超える場合は、乳化時の
安定性が低下し、かつ粘着特性が低下するため好ましく
ない。なお、粘着付与樹脂組成物の酸価を100〜13
0、かつ軟化点を90〜130とすることで粘着特性お
よび乳化特性がより向上するため好ましい。当該粘着付
与樹脂組成物は、通常、ロジン系樹脂、石油系樹脂、テ
ルペン系樹脂、フェノール樹脂、ケトン樹脂などの各種
公知の粘着付与樹脂を単独でまたは数種を混合したもの
を使用できる。
The tackifying resin composition used in the present invention has an acid value of 90 to 220 and a softening point of 80 to 160.
There is no particular limitation as long as it is at a temperature of ° C, and known materials can be used. If the acid value is less than 90, the coatability and adhesive properties will deteriorate, and if it exceeds 220,
It is not preferable because the stability at the time of emulsification is lowered and the adhesive property is lowered. If the softening point is below 80 ° C,
If the adhesive property is lowered and exceeds 160 ° C., the stability at the time of emulsification is lowered and the adhesive property is lowered, which is not preferable. The acid value of the tackifying resin composition is 100 to 13
It is preferable that the softening point is 0 and the softening point is 90 to 130 because the adhesive property and the emulsifying property are further improved. As the tackifying resin composition, various known tackifying resins such as rosin-based resins, petroleum-based resins, terpene-based resins, phenol resins, and ketone resins can be used alone or as a mixture of several kinds.

【0009】ロジン系樹脂としては、ガムロジン、ウッ
ドロジン、トール油ロジン等の原料ロジン;原料ロジン
の不均化物;原料ロジンを水素添加処理した安定化ロジ
ン;重合ロジン等のロジン類や、ロジン類のエステル化
物、フェノール変性物類、不飽和酸変性ロジン類等の各
種公知のものを特に制限なく使用できる。ロジン類のエ
ステル化物とは、前記ロジン類と多価アルコール類をエ
ステル化反応させたものをいう。多価アルコール類とし
ては、例えば、エチレングリコール、ジエチレングリコ
ール、プロピレングリコール、ネオペンチルグリコール
などの2価アルコール;グリセリン、トリメチロールエ
タン、トリメチロールプロパンなどの3価アルコール;
ペンタエリスリトール、ジグリセリンなどの4価アルコ
ール;ジペンタエリスリトールなどの6価アルコール等
が挙げられる。これら多価アルコール類は単独でまたは
数種を併用できる。ロジン類のフェノール変性物類と
は、上記したロジン類に、フェノールやアルキルフェノ
ールなどのフェノール類を付加させたものや、ロジン類
にフェノール類を付加させた後に前記した多価アルコー
ル類を用いてエステル化したもの、ロジン類にレゾール
型フェノール樹脂を反応させた、いわゆるロジン変性フ
ェノール樹脂、およびそのエステル化物等が挙げられ
る。不飽和酸変性ロジン類としては、前記原料ロジンを
マレイン酸、フマル酸、(メタ)アクリル酸(なお、
「(メタ)アクリル」とは「アクリル」または「メタク
リル」のことをいう。以下同様)等の不飽和酸で変性し
た不飽和酸変性ロジンや、そのエステル化物などが挙げ
られ、これら1種を単独で、または2種以上を混合して
使用できる。なお、不飽和酸変性ロジンのエステル化物
とは、前記不飽和酸変性ロジンと前記多価アルコール類
をエステル化反応させたものである。
Examples of rosin-based resins include raw rosins such as gum rosin, wood rosin and tall oil rosin; disproportionated raw rosins; stabilized rosins obtained by hydrogenating raw rosins; rosins such as polymerized rosins and rosins. Various known compounds such as esterified products, phenol modified products and unsaturated acid modified rosins can be used without particular limitation. The esterified product of rosin refers to an esterified product of the rosin and polyhydric alcohol. Examples of polyhydric alcohols include dihydric alcohols such as ethylene glycol, diethylene glycol, propylene glycol and neopentyl glycol; trihydric alcohols such as glycerin, trimethylolethane and trimethylolpropane;
Examples thereof include tetrahydric alcohols such as pentaerythritol and diglycerin; and hexahydric alcohols such as dipentaerythritol. These polyhydric alcohols can be used alone or in combination of several kinds. Phenol-modified products of rosins are those prepared by adding phenols such as phenol and alkylphenol to the above-mentioned rosins, or ester using polyhydric alcohols after adding phenols to rosins. Examples thereof include so-called rosins, so-called rosin-modified phenol resins obtained by reacting rosins with a resol-type phenol resin, and esterified products thereof. As the unsaturated acid-modified rosins, maleic acid, fumaric acid, (meth) acrylic acid (note that the raw material rosin is
“(Meth) acrylic” means “acrylic” or “methacrylic”. The same shall apply hereinafter) and the like, and unsaturated acid-modified rosin modified with an unsaturated acid, its esterified product, etc. may be used alone or in admixture of two or more. The esterified product of unsaturated acid-modified rosin is an esterified product of the unsaturated acid-modified rosin and the polyhydric alcohol.

【0010】石油系樹脂としては、C5系石油樹脂、C
9系石油樹脂、C5−C9共重合系石油樹脂、石油留分
を精製して得られた1種または数種のモノマーを重合さ
せて得られるピュアモノマー樹脂、ジシクロペンタジエ
ン系石油樹脂や、これらの水素化物等を例示できる。
As the petroleum resin, C5 petroleum resin, C
9-based petroleum resin, C5-C9 copolymer-based petroleum resin, pure monomer resin obtained by polymerizing one or several kinds of monomers obtained by purifying petroleum fractions, dicyclopentadiene-based petroleum resin, and these And the like.

【0011】テルペン系樹脂としては、α−ピネン樹
脂、β−ピネン樹脂や、α−ピネン、β−ピネン等のテ
ルペン類とスチレン等の芳香族モノマーを共重合させた
芳香族変性のテルペン系樹脂や、これらの水素化物等を
例示できる。
As the terpene resin, an α-pinene resin, a β-pinene resin, or an aromatic-modified terpene resin obtained by copolymerizing terpenes such as α-pinene and β-pinene with an aromatic monomer such as styrene. And hydrides thereof can be exemplified.

【0012】フェノール樹脂とは、一般に、フェノール
類とホルムアルデヒドの縮合物をいい、フェノール類と
しては、フェノール、m−クレゾール、3,5−キシレ
ノール、p−アルキルフェノール、レゾルシンなどが挙
げられ、これらとホルムアルデヒドをアルカリ触媒で付
加反応させたレゾールや、酸触媒で縮合反応させて得ら
れるノボラック等を例示できる。また、ロジンにフェノ
ールを酸触媒で付加させ熱重合することにより得られる
ロジンフェノール樹脂等も例示できる。
The phenol resin generally refers to a condensate of phenol and formaldehyde, and examples of the phenol include phenol, m-cresol, 3,5-xylenol, p-alkylphenol, resorcin, and the like. Examples thereof include resole obtained by addition reaction of alkanol with an alkali catalyst, and novolac obtained by condensation reaction with an acid catalyst. Further, a rosin phenol resin obtained by adding phenol to rosin with an acid catalyst and thermally polymerizing the same can be exemplified.

【0013】ケトン樹脂とは、メチルエチルケトン、メ
チルイソブチルケトン、アセトフェノン、シクロヘキサ
ノン、またはメチルシクロヘキサノンとホルムアルデヒ
ドの縮合物等をいう。
The ketone resin means methyl ethyl ketone, methyl isobutyl ketone, acetophenone, cyclohexanone, or a condensation product of methylcyclohexanone and formaldehyde.

【0014】これら酸価が90〜220、かつ軟化点が
80〜160℃である粘着付与樹脂組成物としては、不
飽和酸変性ロジン類が好ましく、特に、不飽和酸変性ロ
ジン類と他の粘着付与樹脂の混合物を用いた場合には、
初期接着性および塗工性の向上が著しいため好ましい。
このときに不飽和酸変性ロジン類と併用する粘着付与樹
脂としては、特に制限されないが、ロジン系樹脂を用い
た場合が初期接着性および粘着特性の点から好ましい。
なお、この場合の不飽和酸変性ロジン類含有量として
は、通常70%以下、好ましくは60%以下、更に好ま
しくは50%以下である。含有量が70%を越える場合
には乳化時の安定性が低下し、かつ粘着特性が低下する
傾向にあり適当ではない。
As the tackifying resin composition having an acid value of 90 to 220 and a softening point of 80 to 160 ° C., unsaturated acid-modified rosins are preferable, and particularly unsaturated acid-modified rosins and other adhesives. When a mixture of applied resins is used,
It is preferable because the initial adhesiveness and coatability are remarkably improved.
At this time, the tackifying resin used in combination with the unsaturated acid-modified rosin is not particularly limited, but it is preferable to use a rosin-based resin from the viewpoint of initial adhesiveness and tackiness.
The unsaturated acid-modified rosin content in this case is usually 70% or less, preferably 60% or less, and more preferably 50% or less. If the content exceeds 70%, the stability at the time of emulsification tends to decrease and the adhesive property tends to decrease, which is not suitable.

【0015】本発明で使用する乳化剤としては、重量平
均分子量が10万以下、好ましくは5万以下の各種公知
のアニオン系乳化剤やノニオン系乳化剤を単独でまたは
数種を混合して特に制限無く使用できる。重量平均分子
量を10万以下とすることにより乳化能の低下を防ぎ、
製品粘度が高くなりすぎないため好ましい。例としては
α−オレフィンスルホン化物、アルキルサルフェート、
アルキルフェニルサルフェート、ポリオキシエチレンア
ルキルフェニルエーテルサルフェート、ポリオキシエチ
レンアラルキルフェニルエーテルのスルホコハク酸のハ
ーフエステル塩、アルキルサルコシネート、ロジン石鹸
等のアニオン系乳化剤や、ポリオキシエチレンアルキル
エーテル等のノニオン系乳化剤を例示でき、これらの1
種を単独でまたは2種以上を混合して使用できる。乳化
剤の使用量は、通常粘着付与樹脂100重量部に対し、
固形分換算で1〜10重量部程度、好ましくは1〜5重
量部である。乳化剤の使用量が1重量部より少ない場合
には乳化が困難となり、また、10重量部より多い場合
には耐水性、粘着性能が低下する傾向があるため好まし
くない。
As the emulsifier used in the present invention, various known anionic emulsifiers and nonionic emulsifiers having a weight average molecular weight of 100,000 or less, preferably 50,000 or less are used alone or in combination of several kinds without particular limitation. it can. By setting the weight average molecular weight to 100,000 or less, reduction of emulsifying ability is prevented,
It is preferable because the product viscosity does not become too high. Examples include α-olefin sulfonates, alkyl sulfates,
Alkyl phenyl sulphate, polyoxyethylene alkyl phenyl ether sulphate, polyoxyethylene aralkyl phenyl ether half ester salt of sulfosuccinic acid, alkyl sarcosinate, anionic emulsifiers such as rosin soap and nonionic emulsifiers such as polyoxyethylene alkyl ether And one of these
The seeds may be used alone or in combination of two or more. The amount of emulsifier used is usually 100 parts by weight of tackifying resin,
It is about 1 to 10 parts by weight, preferably 1 to 5 parts by weight in terms of solid content. When the amount of the emulsifier used is less than 1 part by weight, emulsification becomes difficult, and when it is more than 10 parts by weight, water resistance and adhesive performance tend to be deteriorated, which is not preferable.

【0016】粘着付与樹脂の乳化方法は特に制限され
ず、公知の乳化方法である高圧乳化法、反転乳化法、超
音波乳化法、溶剤乳化法などのいずれの方法を採用して
もよいが、完全無溶剤が要求される用途には反転乳化法
を採用すれば良い。反転乳化法の場合は、前記粘着付与
樹脂組成物を軟化点以上で溶融し、これに乳化剤を練り
込んでいき、次いで水を添加して転相させてエマルジョ
ンを得ることができる。
The emulsification method of the tackifying resin is not particularly limited, and any known emulsification method such as a high pressure emulsification method, an inversion emulsification method, an ultrasonic emulsification method and a solvent emulsification method may be adopted. The reverse emulsification method may be adopted for applications where complete solvent-free is required. In the case of the inversion emulsification method, the above tackifying resin composition is melted at a softening point or higher, an emulsifier is kneaded into this, and then water is added to cause phase inversion to obtain an emulsion.

【0017】かくして得られた粘着付与樹脂エマルジョ
ンの固形分濃度は特に限定されないが、通常20〜70
重量%程度となるように適宜に調整して用いる。また、
得られたエマルジョンの平均粒子径は、通常0.1〜2
μm程度であり、大部分は0.5μm以下の粒子として
均一に分散している。また、該エマルジョンは白色ない
し乳白色の外観を呈し、pH値は2〜9程度で、粘度は
通常10〜500mPa・s程度である。
The solid content concentration of the tackifying resin emulsion thus obtained is not particularly limited, but is usually 20 to 70.
It is used by appropriately adjusting it so as to be about% by weight. Also,
The average particle size of the obtained emulsion is usually 0.1 to 2
It is about μm, and most of them are uniformly dispersed as particles of 0.5 μm or less. The emulsion has a white or milky white appearance, a pH value of about 2 to 9 and a viscosity of about 10 to 500 mPa · s.

【0018】本発明の水系粘・接着剤組成物は、アクリ
ル系重合体エマルジョン、ゴム系ラテックスおよび合成
樹脂系エマルジョンからなる群より選ばれる少なくとも
一種のベースポリマーに、前記粘着付与樹脂エマルジョ
ンを配合してなるものである。
The water-based adhesive / adhesive composition of the present invention comprises the tackifying resin emulsion blended with at least one base polymer selected from the group consisting of an acrylic polymer emulsion, a rubber latex and a synthetic resin emulsion. It will be.

【0019】前記粘着付与樹脂エマルジョンと併用する
アクリル系重合体エマルジョンとしては、特に制限はな
く、各種のものを使用できる。当該アクリル系重合体エ
マルジョンは、(メタ)アクリル酸エステルを一括仕込
み重合法、モノマー逐次添加重合法、乳化モノマー逐次
添加重合法、シード重合法等の公知の乳化重合法により
容易に製造することができる。
The acrylic polymer emulsion used together with the tackifying resin emulsion is not particularly limited, and various kinds can be used. The acrylic polymer emulsion can be easily produced by a known emulsion polymerization method such as batch-charging method of (meth) acrylic acid ester polymerization method, monomer sequential addition polymerization method, emulsion monomer sequential addition polymerization method, and seed polymerization method. it can.

【0020】使用される(メタ)アクリル酸エステルと
しては、たとえば、(メタ)アクリル酸メチル、(メ
タ)アクリル酸エチル、(メタ)アクリル酸ブチル、
(メタ)アクリル酸2−エチルヘキシル、(メタ)アク
リル酸グリシジル、(メタ)アクリル酸2−ヒドロキシ
エチル等をあげることができ、これらを単独でもしくは
二種以上を混合して用いる。また、得られるアクリル系
重合体エマルジョンに貯蔵安定性を付与するため、前記
(メタ)アクリル酸エステルに換えて(メタ)アクリル
酸を少量使用してもよい。さらに所望により(メタ)ア
クリル酸エステル重合体の接着特性を損なわない程度
で、たとえば、酢酸ビニル、スチレン等の共重合可能な
モノマーを併用できる。なお、アクリル系重合体エマル
ジョンに用いられる乳化剤としては、アニオン性乳化
剤、ノニオン性乳化剤、部分ケン化ポリビニルアルコー
ル等の各種公知のものを使用でき、その使用量は重合体
100重量部に対して0.1〜5重量部程度、好ましく
は0.5〜3重量部である。
Examples of the (meth) acrylic acid ester used include methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate,
Examples thereof include 2-ethylhexyl (meth) acrylate, glycidyl (meth) acrylate, and 2-hydroxyethyl (meth) acrylate. These may be used alone or in admixture of two or more. Further, in order to impart storage stability to the obtained acrylic polymer emulsion, a small amount of (meth) acrylic acid may be used instead of the (meth) acrylic acid ester. Further, if desired, a copolymerizable monomer such as vinyl acetate or styrene can be used in combination to the extent that the adhesive property of the (meth) acrylic acid ester polymer is not impaired. As the emulsifier used in the acrylic polymer emulsion, various known emulsifiers such as anionic emulsifiers, nonionic emulsifiers and partially saponified polyvinyl alcohol can be used, and the amount thereof is 0 based on 100 parts by weight of the polymer. 0.1 to 5 parts by weight, preferably 0.5 to 3 parts by weight.

【0021】アクリル系重合体エマルジョンと粘着付与
樹脂エマルジョンの使用割合は、アクリル系重合体エマ
ルジョン100重量部(固形分換算)に対して、粘着付
与樹脂エマルジョンを通常10〜100重量部程度(固
形分換算)するのが好ましい。粘着付与樹脂エマルジョ
ンが10重量部に満たない場合には、粘着付与樹脂を添
加することによる改質がほとんど認められない場合があ
り、また100重量部を越える場合には凝集力が低下す
る傾向にある。
The ratio of the acrylic polymer emulsion to the tackifying resin emulsion used is usually about 10 to 100 parts by weight (solid content) with respect to 100 parts by weight (solid content) of the acrylic polymer emulsion. (Converted) is preferable. If the tackifying resin emulsion is less than 10 parts by weight, the modification due to addition of the tackifying resin may hardly be observed, and if it exceeds 100 parts by weight, the cohesive force tends to decrease. is there.

【0022】また、ゴム系ラテックスとしては、水系粘
・接着剤組成物に用いられる各種公知のものを使用でき
る。例えば天然ゴムラテックス、スチレン−ブタジエン
共重合体ラテックス、クロロプレンラテックス等が挙げ
られる。
As the rubber-based latex, various known ones used in water-based adhesive / adhesive compositions can be used. Examples thereof include natural rubber latex, styrene-butadiene copolymer latex, and chloroprene latex.

【0023】ゴム系ラテックスと粘着付与樹脂エマルジ
ョンの使用割合は、ゴム系ラテックス100重量部(固
形分換算)に対して、粘着付与樹脂エマルジョンを通常
10〜150重量部程度(固形分換算)とするのが好ま
しい。粘着付与樹脂エマルジョンが10重量部に満たな
い場合は、粘着付与樹脂を添加することによる改質がほ
とんど認められない場合があり、また150重量部を越
える場合には凝集力が低下する傾向にある。
The use ratio of the rubber-based latex and the tackifying resin emulsion is usually about 10 to 150 parts by weight (solid content) with respect to 100 parts by weight of rubber latex (solid content). Is preferred. If the tackifying resin emulsion is less than 10 parts by weight, the modification due to addition of the tackifying resin may be hardly observed, and if it exceeds 150 parts by weight, the cohesive force tends to decrease. .

【0024】さらに、合成樹脂系エマルジョンとして
は、水系接着剤組成物に用いられる各種公知のものを使
用でき、例えば酢酸ビニル系エマルジョン、エチレン−
酢酸ビニル共重合体エマルジョン、ウレタン系エマルジ
ョン等の合成樹脂エマルジョンがあげられる。
As the synthetic resin emulsion, various known ones used in water-based adhesive compositions can be used, for example, vinyl acetate emulsion and ethylene-based emulsion.
Examples thereof include synthetic resin emulsions such as vinyl acetate copolymer emulsions and urethane emulsions.

【0025】合成樹脂系エマルジョンと粘着付与樹脂エ
マルジョンの使用割合は、合成樹脂系エマルジョン10
0重量部(固形分換算)に対して、粘着付与樹脂エマル
ジョンの添加量を10〜100重量部程度(固形分換
算)とするのが好ましい。粘着付与樹脂エマルジョンが
10重量部に満たない場合には、粘着付与樹脂を添加す
ることによる改質がほとんど認めらない場合があり、ま
た100重量部を越える場合には凝集力が低下する傾向
にある。
The ratio of the synthetic resin emulsion and the tackifying resin emulsion used is as follows.
It is preferable that the addition amount of the tackifying resin emulsion is about 10 to 100 parts by weight (solid content conversion) with respect to 0 part by weight (solid content conversion). If the tackifying resin emulsion is less than 10 parts by weight, the modification due to the addition of the tackifying resin may hardly be recognized, and if it exceeds 100 parts by weight, the cohesive force tends to decrease. is there.

【0026】本発明の水系接着剤組成物は、アクリル系
重合体エマルジョン、ゴム系ラテックスおよび合成樹脂
系エマルジョンからなる群より選ばれる少なくとも一種
のベースポリマーおよび粘着付与樹脂エマルジョンを必
須成分として構成されるが、これらのほかに、必要に応
じて消泡剤、増粘剤、充填剤、酸化防止剤、耐水化剤、
造膜助剤、保水剤等を添加することができる。
The water-based adhesive composition of the present invention comprises at least one base polymer selected from the group consisting of an acrylic polymer emulsion, a rubber latex and a synthetic resin emulsion and a tackifying resin emulsion as essential components. However, in addition to these, if necessary, antifoaming agent, thickener, filler, antioxidant, water resistance agent,
A film-forming aid, a water retention agent, etc. can be added.

【0027】[0027]

【発明の効果】本発明により得られる粘着付与樹脂エマ
ルジョンは、貯蔵安定性が良好であり、作業性に優れる
などの特徴を有する。また得られた水系接着剤組成物
は、粘着付与樹脂エマルジョンに起因する当該特徴を有
し、しかも優れた初期接着性や塗工性を有する。
EFFECTS OF THE INVENTION The tackifying resin emulsion obtained by the present invention is characterized by good storage stability and excellent workability. Further, the obtained water-based adhesive composition has the characteristics due to the tackifying resin emulsion and has excellent initial adhesiveness and coatability.

【0028】[0028]

【実施例】以下に、製造例、実施例及び比較例を挙げて
本発明を詳細に説明するが、本発明はこれら各例に限定
されるものではない。尚、各例中、部及び%は重量基準
である。
EXAMPLES The present invention will be described in detail below with reference to production examples, examples and comparative examples, but the present invention is not limited to these examples. In each example, parts and% are based on weight.

【0029】製造例1(アクリル系重合体エマルジョン
の製造例) 撹拌装置、還流冷却管、滴下ロートおよび窒素導入管を
備えた四つ口フラスコに、窒素ガス気流下、70℃で、
水43部およびアニオン性乳化剤としてポリオキシエチ
レンアルキルスルホコハク酸2ナトリウム(当該アルキ
ルの炭素数は12〜14、エチレンオキサイドの重合度
7)0.9部を溶解した。また、(1)スチレン20
部、2−エチルヘキシルアクリレート25部およびアク
リル酸2部と、(2)触媒(過硫酸カリウム)0.2
部、pH調整剤(重曹)0.1部および水8.8部を、
それぞれ別々の滴下ロートから、1/10量ずつ滴下
し、70℃で窒素ガス気流下にて30分間予備反応を行
ない、その後、(1)および(2)の9/10量を2時
間かけて滴下重合を行なった。(1)および(2)の全
量を滴下し終った後、70℃で1時間完結反応を行な
い、室温に冷却後、100メッシュ金網ろ過を行ないな
がら取り出し、固形分48.2%のアクリル系重合体エ
マルジョンを得た。
Production Example 1 (Production Example of Acrylic Polymer Emulsion) A four-necked flask equipped with a stirrer, a reflux condenser, a dropping funnel and a nitrogen inlet tube was placed under a nitrogen gas stream at 70 ° C.
43 parts of water and 0.9 part of disodium polyoxyethylene alkyl sulfosuccinate as the anionic emulsifier (the alkyl has 12 to 14 carbon atoms and the degree of polymerization of ethylene oxide is 7) were dissolved. Also, (1) styrene 20
Part, 2-ethylhexyl acrylate 25 parts and acrylic acid 2 parts, and (2) catalyst (potassium persulfate) 0.2
Parts, pH adjusting agent (baking soda) 0.1 parts and water 8.8 parts,
From each separate dropping funnel, 1/10 amount was added dropwise, and a preliminary reaction was performed at 70 ° C. under a nitrogen gas stream for 30 minutes, and then 9/10 amounts of (1) and (2) were taken over 2 hours. Dropwise polymerization was performed. After the addition of all the amounts of (1) and (2) was completed, the reaction was completed at 70 ° C. for 1 hour, cooled to room temperature, and then taken out through 100 mesh wire mesh filtration to obtain an acrylic-based polymer with a solid content of 48.2%. A combined emulsion was obtained.

【0030】実施例1 重合ロジンエステル(商品名「ペンセルD−125」:
軟化点125℃:酸価15;荒川化学工業(株)製)6
0部とマレイン化変性ロジン(商品名「SS−14」:
軟化点110℃:酸価285;荒川化学工業(株)製)
40部からなる粘着付与樹脂組成物を、180℃にて約
1時間溶融した後、150℃まで冷却した。次いでアニ
オン性乳化剤(商品名「モノゲンY−100」、第一工
業製薬(株)製)5部添加し、加圧条件下で120℃、
60分混練りを行った。更に水105部を添加し10分
間攪拌することにより、固形分50%の粘着付与樹脂の
エマルジョンを得た。
Example 1 Polymerized rosin ester (trade name "Pencel D-125":
Softening point 125 ° C .: Acid value 15; Arakawa Chemical Industry Co., Ltd.) 6
0 parts and maleic modified rosin (trade name "SS-14":
Softening point 110 ° C: Acid value 285; Arakawa Chemical Industry Co., Ltd.)
A tackifying resin composition consisting of 40 parts was melted at 180 ° C. for about 1 hour and then cooled to 150 ° C. Next, 5 parts of an anionic emulsifier (trade name “Monogen Y-100”, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) was added, and 120 ° C. under pressure.
Kneading was performed for 60 minutes. Further, 105 parts of water was added and stirred for 10 minutes to obtain an emulsion of a tackifying resin having a solid content of 50%.

【0031】実施例2 実施例1において、粘着付与樹脂組成物を、重合ロジン
エステル(商品名「ペンセルD−125」:軟化点12
5℃:酸価15;荒川化学工業(株)製)40部とマレ
イン化変性ロジン(商品名「SS−14」:軟化点11
0℃:酸価285;荒川化学工業(株)製)60部に代
えて用いた以外は実施例1と同様にして粘着付与樹脂の
エマルジョンを得た。
Example 2 In Example 1, the tackifying resin composition was prepared by polymerizing rosin ester (trade name "Pencel D-125": softening point 12).
5 ° C .: acid value 15; Arakawa Chemical Industries Co., Ltd. 40 parts and maleated modified rosin (trade name “SS-14”: softening point 11)
0 ° C .: Acid value 285; manufactured by Arakawa Chemical Industry Co., Ltd.) In the same manner as in Example 1 except that 60 parts were used to obtain a tackifying resin emulsion.

【0032】実施例3 実施例1において、粘着付与樹脂組成物を、重合ロジン
エステル(商品名「ペンセルD−125」:軟化点12
5℃:酸価15;荒川化学工業(株)製)30部とマレ
イン化変性ロジン(商品名「SS−14」:軟化点11
0℃:酸価285;荒川化学工業(株)製)70部に代
えて用いた以外は実施例1と同様にして粘着付与樹脂の
エマルジョンを得た。
Example 3 In Example 1, the tackifying resin composition was prepared by polymerizing rosin ester (trade name "Pencel D-125": softening point 12).
5 ° C .: Acid value 15; Arakawa Chemical Co., Ltd. 30 parts and maleated modified rosin (trade name “SS-14”: softening point 11)
An emulsion of a tackifying resin was obtained in the same manner as in Example 1 except that 70 parts of 0 ° C .: acid value of 285; manufactured by Arakawa Chemical Industry Co., Ltd. was used.

【0033】実施例4 実施例1において、粘着付与樹脂組成物を、ロジンエス
テル(商品名「ペンセルGA−90」:軟化点90℃:
酸価3;荒川化学工業(株)製)60部とマレイン化変
性ロジン(商品名「SS−14」:軟化点110℃:酸
価285;荒川化学工業(株)製)40部に代え、15
0℃にて約1時間溶融した後、100℃まで冷却した以
外は実施例1と同様にして粘着付与樹脂のエマルジョン
を得た。
Example 4 In Example 1, the tackifying resin composition was treated with a rosin ester (trade name "Pencel GA-90": softening point 90 ° C .:
Acid value 3; Arakawa Chemical Industry Co., Ltd. 60 parts and maleic modified rosin (trade name "SS-14": softening point 110 ° C .: acid value 285; Arakawa Chemical Industry Co., Ltd.) 40 parts, 15
An emulsion of the tackifying resin was obtained in the same manner as in Example 1 except that the mixture was melted at 0 ° C for about 1 hour and then cooled to 100 ° C.

【0034】実施例5 実施例1において、粘着付与樹脂組成物を、フマル化ロ
ジンエステル(商品名「マルキードNo.30A」:軟
化点115℃:酸価190;荒川化学工業(株)製)に
代えて用いた以外は実施例1と同様にして粘着付与樹脂
のエマルジョンを得た。
Example 5 In Example 1, the tackifying resin composition was applied to a fumarized rosin ester (trade name "Marquide No. 30A": softening point 115 ° C: acid value 190; manufactured by Arakawa Chemical Industry Co., Ltd.). An emulsion of the tackifying resin was obtained in the same manner as in Example 1 except that the emulsion was used instead.

【0035】比較例1 実施例1において、粘着付与樹脂組成物を、重合ロジン
エステル(商品名「ペンセルD−125」:軟化点12
5℃:酸価15;荒川化学工業(株)製)10部とマレ
イン化変性ロジン(商品名「SS−14」:軟化点11
0℃:酸価285;荒川化学工業(株)製)90部に代
えて用いた以外は実施例1と同様にして粘着付与樹脂の
エマルジョンを得た。
Comparative Example 1 In Example 1, the tackifying resin composition was prepared by polymerizing rosin ester (trade name "Pencel D-125": softening point 12).
5 ° C .: acid value 15; Arakawa Chemical Co., Ltd. 10 parts and maleated modified rosin (trade name “SS-14”: softening point 11)
0 ° C .: Acid value 285; manufactured by Arakawa Chemical Industry Co., Ltd.) An emulsion of a tackifying resin was obtained in the same manner as in Example 1 except that 90 parts were used.

【0036】比較例2 実施例1において、粘着付与樹脂組成物を、重合ロジン
エステル(商品名「ペンセルD−125」:軟化点12
5℃:酸価15;荒川化学工業(株)製)に代えて用い
た以外は実施例1と同様にして粘着付与樹脂のエマルジ
ョンを得た。
Comparative Example 2 In Example 1, the tackifying resin composition was prepared by polymerizing rosin ester (trade name "Pencel D-125": softening point 12).
5 ° C .: Acid value 15; A tackifying resin emulsion was obtained in the same manner as in Example 1 except that it was used instead of Arakawa Chemical Industry Co., Ltd.

【0037】比較例3 実施例1において、粘着付与樹脂組成物を、ロジンエス
テル(商品名「スーパーエステルA−75」:軟化点7
5℃:酸価7;荒川化学工業(株)製)に代え、150
℃にて約1時間溶融した後、90℃まで冷却した以外は
実施例1と同様にして粘着付与樹脂のエマルジョンを得
た。
Comparative Example 3 In Example 1, the tackifying resin composition was mixed with rosin ester (trade name "Super Ester A-75": softening point 7).
5 ° C: Acid value 7; 150 in place of Arakawa Chemical Industry Co., Ltd.
An emulsion of a tackifying resin was obtained in the same manner as in Example 1 except that the mixture was melted at 90 ° C for about 1 hour and then cooled to 90 ° C.

【0038】比較例4 実施例1において、粘着付与樹脂組成物を、ガムロジン
(軟化点75℃:酸価175)に代え、150℃にて約
1時間溶解した後、90℃まで冷却した以外は実施例1
と同様にして粘着付与樹脂のエマルジョンを得た。
Comparative Example 4 Except that the tackifying resin composition in Example 1 was replaced with gum rosin (softening point 75 ° C .: acid value 175), the mixture was dissolved at 150 ° C. for about 1 hour and then cooled to 90 ° C. Example 1
An emulsion of the tackifying resin was obtained in the same manner as in.

【0039】比較例5 実施例1において、粘着付与樹脂組成物を、ロジンエス
テル(商品名「KE−364C」:液状:酸価35;荒
川化学工業(株)製)に代え、60℃にて約1時間保温
した後、55℃まで冷却した以外は実施例1と同様にし
て粘着付与樹脂のエマルジョンを得た。
Comparative Example 5 In Example 1, the tackifying resin composition was replaced with a rosin ester (trade name "KE-364C": liquid: acid value 35; manufactured by Arakawa Chemical Industry Co., Ltd.) at 60 ° C. An emulsion of a tackifying resin was obtained in the same manner as in Example 1 except that the temperature was kept for about 1 hour and then cooled to 55 ° C.

【0040】[0040]

【表1】 [Table 1]

【0041】実施例および比較例で行った、粘着付与樹
脂のエマルジョン化における作業性の良否(問題無くエ
マルジョン調製が可能かどうか)を目視判定した。判定
結果を表2に示す。 〇:問題無し。(乳化性良好) △:やや問題あり。(乳化性やや不良(少量の凝集物の
発生が見られる)) ×:問題あり。(乳化性不良(凝集物の発生が多く見ら
れる))
The workability in the emulsification of the tackifier resin (whether or not the emulsion can be prepared without problems), which was carried out in Examples and Comparative Examples, was visually judged. The judgment results are shown in Table 2. ◯: No problem. (Good emulsification property) Δ: Some problem. (Slightly poor emulsifiability (a small amount of aggregates are observed)) x: There is a problem. (Poor emulsifiability (many aggregates are seen))

【0042】実施例および比較例で行った、粘着付与樹
脂のエマルジョン化における貯蔵安定性の良否を40℃
の恒温槽中に2週間静置後、粘度、pH及び粒子径の経
時変化を測定した。判定結果を表2に示す。 〇:変化なし △:若干変化あり ×:変化あり
The storage stability in the emulsification of the tackifying resin was 40 ° C.
After standing in the constant temperature bath for 2 weeks, changes in viscosity, pH and particle size with time were measured. The judgment results are shown in Table 2. ◯: No change △: Slight change X: Change

【0043】[0043]

【表2】 [Table 2]

【0044】水系粘着剤組成物の性能評価 製造例1で得られたアクリル系重合体エマルジョン10
0部(固形換算)に、前記実施例および比較例で得られ
た粘着付与樹脂エマルジョン70部(固形換算)を混合
した調製物に、さらに充填剤(商品名「エスカロン#1
00」、三共精粉(株)製)125部(固形換算)、保
水剤(商品名「トリプロピレングリコール」、東京化成
工業(株)製)10部、増粘剤(商品名「プライマルA
SE−60」、日本アクリル社(株)製)0.5部(固
形換算)を添加しアンモニア水にて増粘させて接着剤組
成物を得た。得られた水系接着剤組成物を、以下の性能
評価方法にて各種試験を行った。
Performance Evaluation of Aqueous Adhesive Composition Acrylic polymer emulsion 10 obtained in Production Example 1
A preparation prepared by mixing 0 parts (solid basis) with 70 parts (solid basis) of the tackifying resin emulsions obtained in the above Examples and Comparative Examples was further added with a filler (trade name "ESCALON # 1".
00 ", manufactured by Sankyo Seiko Co., Ltd., 125 parts (solid basis), water retention agent (trade name" Tripropylene glycol ", manufactured by Tokyo Kasei Kogyo Co., Ltd.) 10 parts, thickener (trade name" Primal A ").
SE-60 "(manufactured by Japan Acrylic Co., Ltd.) 0.5 part (solid basis) was added and thickened with aqueous ammonia to obtain an adhesive composition. Various tests were performed on the obtained water-based adhesive composition by the following performance evaluation methods.

【0045】(接着性能試験)以下の試験方法により接
着特性を評価した。 (1)塗布性 上記水系接着剤組成物を繊維強化セメント板の平滑面へ
の塗布性をこて伸び、くし目立ち及びこて切れを相対的
に目視評価した。評価結果を表3に示す。 ○:良好 △:若干不良(塗布時にたれ等少し有り) ×:不良(塗布時にたれ等有り) (2)初期接着強さ 幅70mm、長さ150mm及び厚さ8mmの繊維強化
セメント板の平滑面にJIS Z 1525に規定する
粘着テープを中央部に30mm幅の接着面が残るように
貼り付け、その面に上記水系接着剤組成物を、くし目ご
てで均一に塗布する。粘着テープは、塗布後直ちに剥が
して取り去る。オープンタイム20分又は60分の後
に、幅25mm、長さ200mmのビニル床シートを貼
り合わせ、ビニル床シートの上から約5kgのハンドロ
ーラーで2回往復して圧着後、ビニル床シート上面に1
cm2当たり質量10gの重りを載せ1時間養生する。
その後、ビニル床シートの片端に200gの重りを吊る
し、90度ではく離した時の全面はく離するまでの時間
を測定した。評価結果を表3に示す。 (3)90度はく離接着強さ 養生時間を168時間に変更した以外は初期接着性と同
様の方法により試験片を作成した。その後、90度はく
離接着強さ試験用ジグを用いて変位速度200mm/m
inで90度はく離接着強さを測定した。評価結果を表
4に示す。 (4)引張接着強さ 鋼製アタッチメントに幅40mm、長さ40mmのビニ
ル床タイルの平滑面を接着剤(商品名「ボンドクイック
メンダー」、コニシ(株)製)で接着加工し、試験用床
タイルを作成した。幅70mm、長さ70mm及び厚さ
8mmの繊維強化セメント板の平滑面に上記水系接着剤
組成物を適当量載せ、くし目ごてで均一に塗布する。オ
ープンタイム20分又は60分の後に、試験用床タイル
を載せ、更に、試験用床タイルの上に質量1kgの重り
を5秒間載せた後、重りを取り除き、168時間養生す
る。その後、引張強さ試験用ジグを用いて変位速度3m
m/minで引張接着強さを測定した。評価結果を表4
に示す。
(Adhesive Performance Test) The adhesive properties were evaluated by the following test methods. (1) Coatability The coatability of the above water-based adhesive composition to the smooth surface of the fiber-reinforced cement plate was trowel-stretched, and comb-out and trowel breakage were relatively visually evaluated. The evaluation results are shown in Table 3. ◯: Good Δ: Slightly bad (slightly dripping during application) X: Bad (slightly dripping during application) (2) Initial adhesive strength Width 70 mm, length 150 mm and thickness 8 mm Smooth surface of cement board Then, a pressure-sensitive adhesive tape defined in JIS Z 1525 is attached so that an adhesive surface having a width of 30 mm remains in the central part, and the above water-based adhesive composition is uniformly applied to the surface with a comb edge. The adhesive tape should be peeled off immediately after application. After 20 minutes or 60 minutes of open time, a vinyl floor sheet with a width of 25 mm and a length of 200 mm is stuck together, and after reciprocating twice with a hand roller of about 5 kg from above the vinyl floor sheet, pressure bonding, and then 1 on the top surface of the vinyl floor sheet.
A weight with a mass of 10 g per cm 2 is placed and cured for 1 hour.
Then, a weight of 200 g was hung on one end of the vinyl floor sheet, and the time until peeling off the entire surface at 90 ° was measured. The evaluation results are shown in Table 3. (3) 90 degree peeling adhesive strength A test piece was prepared in the same manner as the initial adhesiveness except that the curing time was changed to 168 hours. Then, using a jig for 90 degree peeling adhesion strength test, the displacement speed is 200 mm / m.
The 90 degree peel adhesion strength was measured in. The evaluation results are shown in Table 4. (4) Tensile bond strength Steel attachments are bonded to the smooth surface of vinyl floor tiles with a width of 40 mm and a length of 40 mm with an adhesive (trade name "Bond Quick Mender", manufactured by Konishi Co., Ltd.), and the test floor is used. Created a tile. An appropriate amount of the above water-based adhesive composition is placed on a smooth surface of a fiber-reinforced cement plate having a width of 70 mm, a length of 70 mm and a thickness of 8 mm, and the mixture is uniformly applied with a comb edge. After the opening time of 20 minutes or 60 minutes, the test floor tile is placed, and a weight having a mass of 1 kg is placed on the test floor tile for 5 seconds, and then the weight is removed and curing is performed for 168 hours. After that, using a jig for tensile strength test, displacement speed 3m
The tensile adhesive strength was measured at m / min. Table 4 shows the evaluation results
Shown in.

【0046】[0046]

【表3】 [Table 3]

【0047】[0047]

【表4】 [Table 4]

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 粘着付与樹脂、乳化剤および水からなる
粘着付与樹脂エマルジョンにおいて、粘着付与樹脂とし
て酸価が90〜220、かつ軟化点が80〜160℃の
粘着付与樹脂組成物を使用することを特徴とする粘着付
与樹脂エマルジョン。
1. A tackifier resin emulsion comprising a tackifier resin, an emulsifier and water, wherein a tackifier resin composition having an acid value of 90 to 220 and a softening point of 80 to 160 ° C. is used. Characterized tackifying resin emulsion.
【請求項2】 粘着付与樹脂組成物が、不飽和酸変性ロ
ジン類を含有することを特徴とする請求項1に記載の粘
着付与樹脂エマルジョン。
2. The tackifying resin emulsion according to claim 1, wherein the tackifying resin composition contains unsaturated acid-modified rosins.
【請求項3】 粘着付与樹脂組成物中の不飽和酸変性ロ
ジン類の含有量が70重量%以下である請求項2に記載
の粘着付与樹脂エマルジョン。
3. The tackifying resin emulsion according to claim 2, wherein the content of the unsaturated acid-modified rosin in the tackifying resin composition is 70% by weight or less.
【請求項4】 アクリル系重合体エマルジョン、ゴム系
ラテックスおよび合成樹脂系エマルジョンからなる群よ
り選ばれる少なくとも一種のベースポリマーと請求項1
〜3のいずれかに記載の粘着付与樹脂エマルジョンとを
含有してなることを特徴とする水系接着剤組成物。
4. At least one base polymer selected from the group consisting of acrylic polymer emulsion, rubber latex and synthetic resin emulsion.
4. A water-based adhesive composition comprising the tackifying resin emulsion according to any one of 3 to 3.
【請求項5】 アクリル系重合体エマルジョンおよび/
または合成樹脂系エマルジョン100重量部(固形分換
算)に対して、請求項1〜3のいずれかに記載の粘着付
与樹脂エマルジョン10〜100重量部(固形分換算)
を配合してなる請求項4に記載の水系接着剤組成物。
5. An acrylic polymer emulsion and / or
Alternatively, 10 to 100 parts by weight of the tackifying resin emulsion according to any one of claims 1 to 3 (based on the solid content) relative to 100 parts by weight of the synthetic resin emulsion (based on the solid content).
The water-based adhesive composition according to claim 4, which comprises:
【請求項6】 ゴム系ラテックス100重量部(固形分
換算)に対して、請求項1〜3のいずれかに記載の粘着
付与樹脂エマルジョン10〜150重量部(固形分換
算)を配合してなる請求項4に記載の水系接着剤組成
物。
6. A composition comprising 10 to 150 parts by weight (as solid content) of the tackifying resin emulsion according to claim 1 to 100 parts by weight (as solid content) of a rubber latex. The water-based adhesive composition according to claim 4.
JP2002146537A 2002-05-21 2002-05-21 Tackifying resin emulsion and aqueous adhesive composition Expired - Lifetime JP3925302B2 (en)

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