JP2003268298A - Heat-resistant adhesive - Google Patents

Heat-resistant adhesive

Info

Publication number
JP2003268298A
JP2003268298A JP2002076909A JP2002076909A JP2003268298A JP 2003268298 A JP2003268298 A JP 2003268298A JP 2002076909 A JP2002076909 A JP 2002076909A JP 2002076909 A JP2002076909 A JP 2002076909A JP 2003268298 A JP2003268298 A JP 2003268298A
Authority
JP
Japan
Prior art keywords
adhesive
group
heat
containing monomer
polar group
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.)
Pending
Application number
JP2002076909A
Other languages
Japanese (ja)
Inventor
Masahiro Ikeda
昌弘 池田
Hideki Goto
英樹 後藤
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP2002076909A priority Critical patent/JP2003268298A/en
Publication of JP2003268298A publication Critical patent/JP2003268298A/en
Pending legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide an adhesive usable under the environment of high temperature, whose adhesive strength is proper to surely fix a low rigidity material to a supporter when the material is subjected to processing and to easily separate it after the processing without giving damage and deformation thereto, and, in addition, no adhesive sticks or remains onto the separated material. <P>SOLUTION: The heat-resistant adhesive is composed mainly of a (meth) acrylic compound obtained by copolymerizing a monomer containing an acryloyl or methacryloyl group with a monomer containing a polar group and having an average molecular weight of 100,000-2,000,000, and a crossliking agent. The adhesive strength of its adhesive layer is 0.1-3.5 N/25 mm by JIS Z0237 after the treatment of heating for 6 hours at 180°C. <P>COPYRIGHT: (C)2003,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、高温環境下で使用
できる粘着剤に関するものである。
TECHNICAL FIELD The present invention relates to an adhesive which can be used in a high temperature environment.

【0002】[0002]

【従来の技術】プラスチックフィルムあるいは薄いガラ
ス板等の剛性が低い材料は破損し易い、或いはその切
断、搬送等の加工時にたわみ、平面を保つことが出来な
い等の理由から、平面を保つことのできる支持体に固定
して加工される。この固定手段としては、脱着が容易な
ことから吸引固定または粘着剤による固定といった方法
が採用されている。
2. Description of the Related Art A material having low rigidity such as a plastic film or a thin glass plate is liable to be broken, or is bent during processing such as cutting or conveying, and cannot be kept flat. It is processed by fixing it to a support that can be made. As the fixing means, a method such as suction fixing or fixing with an adhesive is adopted because it can be easily attached and detached.

【0003】しかしながら、吸引固定の場合は、作業中
にずれが生じたり、吸引の強さによっては材料が変形・
破損する恐れがある。
[0003] However, in the case of suction fixation, a shift may occur during work, or the material may be deformed or deformed depending on the strength of suction.
It may be damaged.

【0004】また、粘着剤により支持体に固定する方法
は、高温処理といった過酷な条件下では被支持体が剥離
したり、あるいは逆に固定後の脱着が困難で、脱着時に
被支持体が変形・損傷したりすることがあった。
Further, in the method of fixing to a support with an adhesive, the support is peeled off under severe conditions such as high temperature treatment, or conversely, it is difficult to remove the support after fixing, and the support is deformed during the removal.・ It was sometimes damaged.

【0005】[0005]

【発明が解決しようとする課題】本発明は上記の欠点を
解決するためになされたものであり、その目的とすると
ころは、薄いガラス板あるいはプラスチックフィルム等
の剛性が低い材料を、加工時には支持体に確実に固定
し、加工後支持体から剥離する必要性が生じた場合は、
材料に損傷を与えたり変形させることなく極めて容易に
剥離することができる適度な強度で固定することがで
き、しかも剥離後、材料に付着・残留しない高温環境下
で使用できる粘着剤を提供することにある。
SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned drawbacks, and an object thereof is to support a material having low rigidity such as a thin glass plate or a plastic film during processing. If it is necessary to firmly fix it to the body and peel it from the support after processing,
To provide a pressure-sensitive adhesive that can be fixed with an appropriate strength that can be peeled very easily without damaging or deforming the material, and that can be used in a high temperature environment that does not adhere to or remain on the material after peeling. It is in.

【0006】[0006]

【課題を解決するための手段】すなわち本発明は、アク
リロイル基またはメタクリロイル基含有モノマーと、極
性基含有モノマーを共重合してなる平均分子量が10万〜
200万の(メタ)アクリル系化合物、及び架橋剤を主成
分とし、180℃、6時間加熱処理後の加熱処理後のJ
IS Z 0237による該粘着剤層の粘着強度が0.
1〜3.5N/25mmであることを特徴とする請求項1記
載の耐熱性粘着剤。 (2)極性基含有モノマーの極性基がカルボキシル基、
水酸基、アミノ基より選ばれる極性基である請求項1記
載の耐熱性粘着剤。である。
Means for Solving the Problems That is, the present invention has an average molecular weight of 100,000 to 100,000 obtained by copolymerizing an acryloyl group- or methacryloyl group-containing monomer and a polar group-containing monomer.
2 million (meth) acrylic compounds and cross-linking agent as main components, J after heat treatment after heat treatment at 180 ° C for 6 hours
The adhesive strength of the adhesive layer according to IS Z 0237 is 0.
The heat-resistant pressure-sensitive adhesive according to claim 1, wherein the heat-resistant pressure-sensitive adhesive is 1 to 3.5 N / 25 mm. (2) The polar group of the polar group-containing monomer is a carboxyl group,
The heat-resistant adhesive according to claim 1, which is a polar group selected from a hydroxyl group and an amino group. Is.

【0007】[0007]

【発明の実施の形態】次に本発明の耐熱性粘着剤につい
て詳細に説明する。本発明者らは、高温環境下において
も適度な粘着性を保つことができるよう種々の検討を行
った結果、平均分子量が10万〜200万の(メタ)アクリ
ル系共重合体を架橋させることで、上記の目的が達成で
きることを確認した。
BEST MODE FOR CARRYING OUT THE INVENTION Next, the heat-resistant adhesive of the present invention will be described in detail. The present inventors have conducted various studies so as to be able to maintain appropriate tackiness even in a high temperature environment, and as a result, crosslink a (meth) acrylic copolymer having an average molecular weight of 100,000 to 2,000,000. It was confirmed that the above objectives could be achieved.

【0008】加工時に浮きや剥離を生じさせず、加工後
に着脱が容易な粘着力としては、JIS Z 0237
による粘着力が0.1〜3.5N/25mmの範囲であるこ
とが好ましく、さらに好ましくは、1.5〜3.3N/25
mm、最も好ましくは2.0〜3.0N/25mmである。本
発明の耐熱性粘着剤は、耐熱性、特に高温での保持力に
優れ、材料と支持体とを必要かつ十分な接着強度で接着
させる。しかも、この接着強度が加熱により過度に高く
ならない。従って、材料を支持体から剥離する必要性が
生じた場合は、材料に損傷を与えたり変形させることな
く極めて容易に剥離することができ、しかも材料上に粘
着剤が残存しにくいという今までにない特徴をもつもの
である。
[0008] JIS Z 0237 has an adhesive force that does not cause floating or peeling during processing and is easy to attach and detach after processing.
It is preferable that the adhesive strength is in the range of 0.1 to 3.5 N / 25 mm, and more preferably 1.5 to 3.3 N / 25.
mm, most preferably 2.0 to 3.0 N / 25 mm. The heat-resistant pressure-sensitive adhesive of the present invention is excellent in heat resistance, especially holding power at high temperature, and bonds the material and the support with necessary and sufficient adhesive strength. Moreover, this adhesive strength does not become excessively high due to heating. Therefore, when it becomes necessary to peel the material from the support, it can be peeled very easily without damaging or deforming the material, and the adhesive does not easily remain on the material. It has a unique feature.

【0009】本発明において用いられる(メタ)アクリ
ル系共重合体は、アクリロイル基またはメタクリロイル
基含有モノマーと極性基含有モノマーの共重合体であ
る。極性基含有モノマーが添加されることにより、本発
明の粘着剤は、支持体、特にガラス基板との十分な密着
性を得ることが出来る。アクリロイル基またはメタクリ
ロイル基含有モノマーとしては、例えば、2−エチルへ
キシルアクリレート、シクロへキシルアクリレート等が
挙げられるが、特にこれらに限定されるものではない。
The (meth) acrylic copolymer used in the present invention is a copolymer of an acryloyl group- or methacryloyl group-containing monomer and a polar group-containing monomer. By adding the polar group-containing monomer, the pressure-sensitive adhesive of the present invention can obtain sufficient adhesion to a support, particularly a glass substrate. Examples of the acryloyl group- or methacryloyl group-containing monomer include 2-ethylhexyl acrylate and cyclohexyl acrylate, but are not particularly limited thereto.

【0010】本発明で使用する極性基含有モノマーとし
ては、アクリル酸、メタクリル酸、アクリル酸ジメチ
ル、アクリロ二トリル、等に挙げられる、分子中にカル
ボキシル基、水酸基、アミノ基等の極性基を有する重合
性不飽和モノマーが好ましく、2−ヒドロキシエチルア
クリレート、β―カルボキシエチルアクリレート、メタ
クリル酸2−ヒドロキシエチル、メタクリル酸2−ヒド
ロキシプロピル、アクリロ二トリル、メタクリロ二トリ
ル、N−ビニル−2−ピロリドン等が挙げられる。
The polar group-containing monomer used in the present invention includes acrylic acid, methacrylic acid, dimethyl acrylate, acrylonitrile and the like, and has polar groups such as carboxyl group, hydroxyl group and amino group in the molecule. Polymerizable unsaturated monomers are preferable, such as 2-hydroxyethyl acrylate, β-carboxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, acrylonitrile, methacrylonitrile, and N-vinyl-2-pyrrolidone. Is mentioned.

【0011】本発明において用いられる(メタ)アクリ
ル系共重合体は、上記極性基含有モノマーから誘導され
る繰り返し単位を通常0.5〜30重量%、好ましくは3〜10
重量%の量で有しているのが望ましい。
The (meth) acrylic copolymer used in the present invention usually contains a repeating unit derived from the above polar group-containing monomer in an amount of 0.5 to 30% by weight, preferably 3 to 10% by weight.
It is desirable to have it in an amount of% by weight.

【0012】本発明において用いられる(メタ)アクリ
ル系共重合体の平均分子量は10万〜200万であり、好ま
しくは、50万〜100万である。上記(メタ)アクリル系共
重合体の平均分子量が最小値より小さい場合には、18
0℃、6時間加熱処理後の保持力が低下するため好まし
くない。また、平均分子量が最大値より大きい場合に
は、特性上は問題ないが、(メタ)アクリル系共重合体
を量産することが難しく、好ましくない。
The average molecular weight of the (meth) acrylic copolymer used in the present invention is 100,000 to 2,000,000, preferably 500,000 to 1,000,000. When the average molecular weight of the (meth) acrylic copolymer is smaller than the minimum value, 18
It is not preferable because the holding power after heat treatment at 0 ° C. for 6 hours decreases. Further, when the average molecular weight is larger than the maximum value, there is no problem in characteristics, but it is difficult to mass-produce the (meth) acrylic copolymer, which is not preferable.

【0013】上記(メタ)アクリル系共重合体は、ラジ
カル重合、溶液重合、乳化重合、懸濁重合、塊状重合等
のアクリル系共重合体が合成される通常の重合方法によ
って得ることが出来る。
The above-mentioned (meth) acrylic copolymer can be obtained by a usual polymerization method such as radical polymerization, solution polymerization, emulsion polymerization, suspension polymerization, bulk polymerization and the like for synthesizing an acrylic copolymer.

【0014】本発明の粘着剤には加熱処理による硬化を
行わせる為に、ポリイソシアネート化合物、エポキシ化
合物等の架橋剤を添加する。これらの架橋剤の添加量
は、特に限定はしないが、前述の(メタ)アクリル系共
重合体100重量部に対して0.1〜5重量部が好ましく、さ
らに好ましくは0.5〜2重量部である。添加量が下限値未
満の場合は硬化を十分に完了させることが難しく、また
その添加量が5.0重量部より多い場合には、高温での保
持力が低下することがある。
A crosslinking agent such as a polyisocyanate compound or an epoxy compound is added to the pressure-sensitive adhesive of the present invention in order to cure it by heat treatment. The addition amount of these crosslinking agents is not particularly limited, but is preferably 0.1 to 5 parts by weight, more preferably 0.5 to 2 parts by weight, based on 100 parts by weight of the above-mentioned (meth) acrylic copolymer. If the addition amount is less than the lower limit value, it is difficult to sufficiently complete the curing, and if the addition amount is more than 5.0 parts by weight, the holding power at high temperature may decrease.

【0015】また本発明の粘着剤には、粘着強度を高め
るために、発明の目的を損なわない範囲内で、ロジン樹
脂、テルペン樹脂、クマロン樹脂、フェノール樹脂、ス
チレン樹脂、脂肪族系石油樹脂、芳香族系石油樹脂、脂
肪族芳香族共重合系石油樹脂等の粘着付与剤等を添加し
てもよい。
The adhesive of the present invention has a rosin resin, a terpene resin, a coumarone resin, a phenol resin, a styrene resin, an aliphatic petroleum resin, in order to enhance the adhesive strength, within the range not impairing the object of the invention. A tackifier such as an aromatic petroleum resin or an aliphatic aromatic copolymer petroleum resin may be added.

【0016】本発明において、粘着剤層の厚さは特に限
定されるものではないが、1〜50μmが好ましい。本発
明の粘着剤層は、粘着剤をそのまま、または適当な有機
溶剤により溶液化した後、支持体に塗工し、例えば80
〜100℃、30秒から1時間程度の加熱処理等により
乾燥させることにより得ることが出来る。
In the present invention, the thickness of the pressure-sensitive adhesive layer is not particularly limited, but is preferably 1 to 50 μm. For the pressure-sensitive adhesive layer of the present invention, the pressure-sensitive adhesive is applied to a support as it is or after being made into a solution with a suitable organic solvent.
It can be obtained by drying by heat treatment or the like at -100 ° C for 30 seconds to 1 hour.

【0017】本発明の粘着剤は、例えばガラス・プラス
チック等を含む支持体の表面に塗布等の手法で粘着剤層
を設け、該粘着剤層を介してガラス基板あるいはプラス
チックフィルム等の被接着体をサーマルラミネート機で
貼り合せることにより仮固定する等により使用できる。
The pressure-sensitive adhesive of the present invention is provided with a pressure-sensitive adhesive layer on the surface of a support containing, for example, glass or plastic by a method such as coating, and an adherend such as a glass substrate or a plastic film via the pressure-sensitive adhesive layer. Can be used by temporarily fixing them by pasting them with a thermal laminating machine.

【0018】[0018]

【実施例】以下本発明を実施例及び比較例により、更に
詳細に説明するが、本発明はこれらに限定するものでは
ない。
EXAMPLES The present invention will be described in more detail with reference to Examples and Comparative Examples, but the present invention is not limited thereto.

【0019】〔実施例1〕2−エチルへキシルアクリレ
ート90重量部と極性基含有モノマーである2−ヒドロキ
シルアクリレート10重量部とを共重合して得られた平均
分子量600000の共重合体100重量部に対し、酢酸エチル5
0重量部を25℃で十分に攪拌し、アクリル系化合物の酢
酸エチル混合溶液を150重量部得た。
Example 1 100 parts by weight of a copolymer having an average molecular weight of 600,000 obtained by copolymerizing 90 parts by weight of 2-ethylhexyl acrylate and 10 parts by weight of 2-hydroxyl acrylate which is a polar group-containing monomer. Against ethyl acetate 5
0 part by weight was sufficiently stirred at 25 ° C. to obtain 150 parts by weight of a mixed solution of an acrylic compound with ethyl acetate.

【0020】次に、上記の反応液150重量部(アクリル系
共重合体100重量部に相当)に、架橋剤として、ポリイソ
シアネ−ト化合物(日本ポリウレタン製:コロネート
L)0.5重量部を添加して十分に攪拌し、本発明の粘着剤
を得た。
Next, 150 parts by weight of the above reaction solution (corresponding to 100 parts by weight of the acrylic copolymer) was added as a crosslinking agent with a polyisocyanate compound (Nippon Polyurethane: Coronate).
L) 0.5 part by weight was added and sufficiently stirred to obtain an adhesive of the present invention.

【0021】上記のようにして得られた粘着剤を乾燥後
の塗布厚が20μmとなるように、中性洗剤で表面を洗
浄した0.7mm厚のガラス板に塗布し、80℃で10
分間乾燥させた。その後、厚さ200μmのポリエーテ
ルサルホン(PES)フィルムを、サーマルラミネ−ター
(エム・シー・ケイ社製)を用いて、圧力:0.7MPa、
温度:25℃の条件でラミネートし接着させた。こうして
接着したPESフィルムとガラス基板との接着力をJI
S Z 0237に準じて粘着強度を測定した。
The pressure-sensitive adhesive obtained as described above was coated on a glass plate having a thickness of 0.7 mm whose surface was washed with a neutral detergent so that the coating thickness after drying was 20 μm, and the temperature was maintained at 80 ° C. for 10 minutes.
Allow to dry for minutes. Then, a 200 μm thick polyether sulfone (PES) film was used with a thermal laminator (manufactured by MKK Co., Ltd.), pressure: 0.7 MPa,
Temperature: 25 ° C. were laminated and adhered. The adhesive strength between the PES film and the glass substrate bonded in this way is determined by JI
The adhesive strength was measured according to SZ0237.

【0022】これらをオーブンにて180℃で6時間加
熱し、その加熱処理中および加熱後のフィルムの剥がれ
・浮きを観察した。同様に加熱処理を行ったPESフィ
ルムとガラス基板との接着力をJIS Z 0237に
準じて粘着強度を測定した。その後、25℃で3分間冷
却してPESフィルムをガラス板から剥離し、そのとき
の剥離のしやすさ、およびPES基板への粘着剤の残留
性(糊残り)を目視観察して評価した。各項目の評価結
果を表1に示す。
These were heated in an oven at 180 ° C. for 6 hours, and the peeling / floating of the film was observed during and after the heat treatment. Similarly, the adhesive strength between the heat-treated PES film and the glass substrate was measured according to JIS Z 0237. Then, the PES film was peeled from the glass plate by cooling at 25 ° C. for 3 minutes, and the ease of peeling at that time and the residual property (adhesive residue) of the adhesive on the PES substrate were visually observed and evaluated. Table 1 shows the evaluation results of each item.

【0023】〔実施例2〕極性基含有モノマーがβ―カ
ルボキシエチルアクリレートである以外は、実施例1と
同様の方法で試料を作製し、実施例1と同様の項目につ
いて試験した。その結果を表1に示す。
Example 2 A sample was prepared in the same manner as in Example 1 except that the polar group-containing monomer was β-carboxyethyl acrylate, and the same items as in Example 1 were tested. The results are shown in Table 1.

【0024】〔実施例3〕実施例1において、アクリロ
イル基含有モノマーとして2−エチルへキシルアクリレ
ート70重量部、ブチルアクリレート20重量部を用い
たこと以外には、実施例1と同様の方法で試料を作製
し、実施例1と同様の項目について試験した。その結果
を表1に示す。
Example 3 A sample was prepared in the same manner as in Example 1 except that 70 parts by weight of 2-ethylhexyl acrylate and 20 parts by weight of butyl acrylate were used as the acryloyl group-containing monomer. Was prepared, and the same items as in Example 1 were tested. The results are shown in Table 1.

【0025】〔比較例1〕実施例1において、2−ヒド
ロキシルアクリレートを添加しないこと以外には、実施
例1と同様の方法で試料を作製し、実施例1と同様の項
目について試験した。その結果を表1に示す。
Comparative Example 1 A sample was prepared in the same manner as in Example 1 except that 2-hydroxyl acrylate was not added, and the same items as in Example 1 were tested. The results are shown in Table 1.

【0026】〔比較例2〕実施例1において、分子量50
000のアクリル系共重合体を用いたこと以外は、実施例
1と同様の方法で試料を作製し、実施例1と同様の項目
について試験した。その結果を表1に示す。
[Comparative Example 2] In Example 1, the molecular weight was 50.
A sample was prepared in the same manner as in Example 1 except that 000 acrylic copolymer was used, and the same items as in Example 1 were tested. The results are shown in Table 1.

【0027】〔比較例3〕実施例1において作成した粘
着剤層の代わりに、接合テープ(商品名:Y−4910
J、住友3M社製)を用いたこと以外は実施例1と同様
の方法で試料を作製し、実施例1と同様の項目について
試験した。その結果を表1に示す。
[Comparative Example 3] Instead of the adhesive layer prepared in Example 1, a joining tape (trade name: Y-4910) was used.
J, manufactured by Sumitomo 3M Ltd.) was used to prepare a sample in the same manner as in Example 1, and the same items as in Example 1 were tested. The results are shown in Table 1.

【0028】[0028]

【表1】 [Table 1]

【0029】[0029]

【発明の効果】本発明によれば、被接着体となるガラス
・プラスチック等をその加工時、搬送時等の工程内にお
いて支持体に必要かつ十分な接着強度で固定することが
出来る為、被接着体に緻密な処理が可能となる。また、
高温条件下においても浮きや剥がれが発生せず、しか
も、この接着強度が加熱などにより過度に高くならな
い。さらに、被接着体を支持体から剥離する必要性が生
じた場合は、被接着体に損傷を与えたり変形することな
く、しかも被支持体上に粘着剤を残さず、極めて容易に
剥離することが可能となる。
EFFECTS OF THE INVENTION According to the present invention, glass, plastic, etc. to be adhered can be fixed to a support with necessary and sufficient adhesive strength during the process of processing, conveying and the like. The adhesive body can be processed in detail. Also,
Floating or peeling does not occur even under high temperature conditions, and the adhesive strength does not become excessively high due to heating or the like. Furthermore, when it becomes necessary to peel the adherend from the support, it is extremely easy to peel without damaging or deforming the adherend and leaving no adhesive on the support. Is possible.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 アクリロイル基またはメタクリロイル基
含有モノマーと、極性基含有モノマーを共重合してなる
平均分子量が10万〜200万の(メタ)アクリル系化合
物、および架橋剤を主成分とし、180℃、6時間加熱
処理後のJIS Z0237による該粘着剤層の粘着強
度が0.1〜3.5N/25mmであることを特徴とする耐
熱性粘着剤。
1. A main component is a (meth) acrylic compound having an average molecular weight of 100,000 to 2,000,000 obtained by copolymerizing an acryloyl group- or methacryloyl group-containing monomer and a polar group-containing monomer, and a crosslinking agent at 180 ° C. A heat-resistant pressure-sensitive adhesive characterized in that the pressure-sensitive adhesive layer according to JIS Z0237 after 6 hours of heat treatment has an adhesive strength of 0.1 to 3.5 N / 25 mm.
【請求項2】 極性基含有モノマーの極性基がカルボキ
シル基、水酸基、アミノ基より選ばれる極性基である請
求項1記載の耐熱性粘着剤。
2. The heat-resistant adhesive according to claim 1, wherein the polar group of the polar group-containing monomer is a polar group selected from a carboxyl group, a hydroxyl group and an amino group.
JP2002076909A 2002-03-19 2002-03-19 Heat-resistant adhesive Pending JP2003268298A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002076909A JP2003268298A (en) 2002-03-19 2002-03-19 Heat-resistant adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002076909A JP2003268298A (en) 2002-03-19 2002-03-19 Heat-resistant adhesive

Publications (1)

Publication Number Publication Date
JP2003268298A true JP2003268298A (en) 2003-09-25

Family

ID=29205498

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002076909A Pending JP2003268298A (en) 2002-03-19 2002-03-19 Heat-resistant adhesive

Country Status (1)

Country Link
JP (1) JP2003268298A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007262320A (en) * 2006-03-29 2007-10-11 Asahi Glass Co Ltd Double-sided pressure sensitive adhesive sheet or tape for glass
JP2018177843A (en) * 2017-04-04 2018-11-15 デンカ株式会社 Adhesive tape and method of manufacturing electronic component

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007262320A (en) * 2006-03-29 2007-10-11 Asahi Glass Co Ltd Double-sided pressure sensitive adhesive sheet or tape for glass
JP2018177843A (en) * 2017-04-04 2018-11-15 デンカ株式会社 Adhesive tape and method of manufacturing electronic component

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