JP6104500B2 - Double-sided adhesive tape - Google Patents
Double-sided adhesive tape Download PDFInfo
- Publication number
- JP6104500B2 JP6104500B2 JP2011149978A JP2011149978A JP6104500B2 JP 6104500 B2 JP6104500 B2 JP 6104500B2 JP 2011149978 A JP2011149978 A JP 2011149978A JP 2011149978 A JP2011149978 A JP 2011149978A JP 6104500 B2 JP6104500 B2 JP 6104500B2
- Authority
- JP
- Japan
- Prior art keywords
- sensitive adhesive
- pressure
- adhesive tape
- double
- support
- 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.)
- Active
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
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- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
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- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 238000009864 tensile test Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XZHNPVKXBNDGJD-UHFFFAOYSA-N tetradecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCOC(=O)C=C XZHNPVKXBNDGJD-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 238000009823 thermal lamination Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000008096 xylene Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Images
Landscapes
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
本発明は、両面粘着テープに関し、特に、携帯用電子機器の筐体や部品の接合部において好適に使用される薄型の両面粘着テープ又はシートに関する。 The present invention relates to a double-sided pressure-sensitive adhesive tape, and more particularly to a thin double-sided pressure-sensitive adhesive tape or sheet that is suitably used in a joint portion of a casing or component of a portable electronic device.
粘着テープは、作業性に優れ、接着信頼性の高い接合手段として、OA機器や家電製品等の各産業分野において部品固定用途等に使用されている。これらOA機器は各種の高機能化と並行して、小型化や薄型化が図られており、パソコンやデジタルビデオカメラ、さらには、電子手帳、携帯電話、PHS、スマートフォン、ゲーム機器、電子書籍等の携帯電子端末においては特に小型化や薄型化の要請が高い。このような携帯電子端末等においては、主要構成部品の薄型化と共に、これらの固定に用いられる粘着テープにおいても薄型化が要求されている。 The adhesive tape has excellent workability and is used as a bonding means with high adhesion reliability in parts fixing applications and the like in various industrial fields such as OA equipment and home appliances. These OA devices have been reduced in size and thickness in parallel with various advanced functions, such as personal computers, digital video cameras, electronic notebooks, mobile phones, PHS, smartphones, game machines, electronic books, etc. In particular, there is a high demand for downsizing and thinning of portable electronic terminals. In such portable electronic terminals and the like, it is required to reduce the thickness of the main component parts and the adhesive tape used for fixing them.
例えば、支持体の両面に粘着剤層を有する両面接着テープ又はシートであって、支持体と、該支持体の両面に形成された2つの粘着剤層との厚みを含む総厚さが3μm以上かつ30μm未満であり、破断強度が2〜26MPa/10mm幅である両面接着テープ又はシートが開示されている(特許文献1)。また例えば、アクリル系の粘着剤を、芯材の両面に有する両面粘着テープであって、該芯材及び両面の粘着剤層を合わせた総厚さが30μm以下であり、両面の粘着剤層の厚さが、2〜10μmである両面粘着テープが開示されている(特許文献2)。 For example, a double-sided adhesive tape or sheet having pressure-sensitive adhesive layers on both sides of the support, the total thickness including the thickness of the support and two pressure-sensitive adhesive layers formed on both sides of the support being 3 μm or more And the double-sided adhesive tape or sheet | seat which is less than 30 micrometers and whose breaking strength is 2-26MPa / 10mm width is disclosed (patent document 1). Further, for example, a double-sided pressure-sensitive adhesive tape having an acrylic pressure-sensitive adhesive on both surfaces of the core material, the total thickness of the core material and the pressure-sensitive adhesive layer on both surfaces is 30 μm or less, A double-sided pressure-sensitive adhesive tape having a thickness of 2 to 10 μm is disclosed (Patent Document 2).
これら粘着テープ又はシートは、その総厚を非常に薄くすることで、薄型化の要請の高い携帯端末機器のクリアランス適合性を図っている。しかし、このような薄型粘着テープは、製造時にシワが入りやすいため、支持体にかかる張力ができるだけ低くなるように調整する工程等を有する製造方法によりシワを抑制しており、生産性が著しく低いものであった。また、薄型テープにおいては、生産時の支持体の送り出しや巻き取り時の切断や、使用時の切断を防ぐため支持体に一定の強度が必要となるが、支持体として樹脂フィルムを使用して薄型且つ高強度とするに際して延伸が行われることから、高温環境下での熱収縮が生じる場合があった。 These pressure-sensitive adhesive tapes or sheets have a very thin total thickness, thereby achieving clearance suitability for portable terminal devices that are highly demanded to be thin. However, since such a thin adhesive tape tends to wrinkle during production, wrinkles are suppressed by a production method including a step of adjusting the tension applied to the support to be as low as possible, and the productivity is extremely low. It was a thing. In addition, in thin tapes, a certain level of strength is required for the support in order to prevent the support from being cut out at the time of production, cutting during use, and cutting during use, but a resin film is used as the support. Since the film is stretched when it is thin and has high strength, heat shrinkage may occur in a high temperature environment.
本発明はこのような事情のもとで、携帯用電子機器の筐体や部品の接合部に用いられる薄型で、生産性・耐熱性に優れる両面粘着テープを提供することを目的としてなされたものである。 Under such circumstances, the present invention was made for the purpose of providing a thin double-sided adhesive tape excellent in productivity and heat resistance, which is used for a joint portion of a casing or component of a portable electronic device. It is.
本発明者らは上記の目的を達成するために鋭意検討した結果、特定の厚み、摩擦抵抗、熱収縮率をもつ芯材を使用することで、本目的を達成できることを見出し、本発明を完成するに至った。 As a result of intensive studies to achieve the above object, the present inventors have found that this object can be achieved by using a core material having a specific thickness, frictional resistance, and heat shrinkage rate, thereby completing the present invention. It came to do.
すなわち、本発明は、樹脂フィルムからなる支持体の両面に、粘着剤層を有する両面粘着テープであって、総厚みが2〜10μmであり、前記支持体の厚みが1〜3μm、熱収縮率が3%以下、動摩擦係数が0.20〜0.28である両面粘着テープを提供する。 That is, the present invention is a double-sided pressure-sensitive adhesive tape having a pressure-sensitive adhesive layer on both sides of a support made of a resin film, the total thickness is 2 to 10 μm, the thickness of the support is 1 to 3 μm, and the heat shrinkage rate Is a double-sided pressure-sensitive adhesive tape having a dynamic friction coefficient of 0.20 to 0.28.
本発明によれば、携帯電子機器の筐体や部品の接合部に用いられる、薄型で生産性・耐熱性に優れる両面粘着テープを提供することができる。 ADVANTAGE OF THE INVENTION According to this invention, the double-sided adhesive tape excellent in productivity and heat resistance used for the junction part of the housing | casing of portable electronic devices or components can be provided.
(両面粘着テープ)
本発明の両面粘着テープは、図1で示されるように、支持体の両面に粘着剤層を有する基材付き両面粘着テープであり、支持体と、該支持体の両面に形成された2つの粘着剤層との厚みを含む総厚みが2μm〜10μmである。このように本発明の粘着テープはきわめて薄く、スペースの少ない電子機器、特に携帯用電子機器の筐体や部品の接合部において好適に使用できる。また基材付きのため、連続的に粘着テープを打ち抜き加工する際にも加工性に優れる。
(Double-sided adhesive tape)
As shown in FIG. 1, the double-sided pressure-sensitive adhesive tape of the present invention is a double-sided pressure-sensitive adhesive tape with a base material having a pressure-sensitive adhesive layer on both sides of the support, and the support and the two formed on both sides of the support The total thickness including the thickness with the pressure-sensitive adhesive layer is 2 μm to 10 μm. As described above, the pressure-sensitive adhesive tape of the present invention is very thin and can be suitably used in the case of an electronic device having a small space, particularly a portable electronic device and a joint part. Moreover, since it has a base material, it is excellent in workability even when the adhesive tape is continuously punched.
図1は、本発明の両面粘着テープの一例を示す概略図である。図1の両面粘着テープにおいて1は支持体、2〜3は粘着剤層、4〜5は剥離ライナーである。両面粘着テープは、支持体1の各面に粘着剤層2、3が形成された構成を有しており、粘着剤層2、3は、各々、剥離ライナー4、5に保護されている。また、当該両面粘着テープは、剥離ライナー4と5とが接触するように重ね合わせられてロール状に巻回された形態とすることもできる。
FIG. 1 is a schematic view showing an example of the double-sided pressure-sensitive adhesive tape of the present invention. In the double-sided pressure-sensitive adhesive tape of FIG. 1, 1 is a support, 2-3 is an adhesive layer, and 4-5 are release liners. The double-sided pressure-sensitive adhesive tape has a structure in which pressure-sensitive
本発明の両面粘着テープの総厚み(テープ厚み)としては、2μm〜10μmであれば特に制限されないが、好ましくは3μm〜7μm、さらに好ましくは3μm〜5μmである。ここで、両面粘着テープの総厚みとは、剥離ライナーを除いた貼り付けに際して使用される厚み、すなわち、一方の粘着剤層表面から他方の粘着剤層表面にかけての厚みをいう。 Although it will not restrict | limit especially if it is 2 micrometers-10 micrometers as total thickness (tape thickness) of the double-sided adhesive tape of this invention, Preferably they are 3 micrometers-7 micrometers, More preferably, they are 3 micrometers-5 micrometers. Here, the total thickness of the double-sided pressure-sensitive adhesive tape refers to the thickness used for attachment excluding the release liner, that is, the thickness from one adhesive layer surface to the other adhesive layer surface.
また、本発明の両面粘着テープの粘着力は特に制限されるものではないが、0.5N/20mm〜12N/20mmが好ましい。さらに好ましくは、1〜8N/20mmである。上記範囲とすることで、接着時のハガレ、リワーク時の剥がしやすさを両立しやすい。粘着力はJISZ0237に準じて測定される。具体的には、ステンレス板(BA板)にPET25μmで裏打ちした粘着テープを貼り合せ、2kgローラーで1往復加圧し、23℃50%RHの条件下で1時間放置し、180°方向に300mm/minの速度で引き剥がし粘着力を測定する。
The adhesive strength of the double-sided pressure-sensitive adhesive tape of the present invention is not particularly limited, but is preferably 0.5 N / 20 mm to 12 N / 20 mm. More preferably, it is 1-8N / 20mm. By setting it as the above range, it is easy to achieve both peeling at the time of adhesion and ease of peeling at the time of rework. The adhesive strength is measured according to JISZ0237. Specifically, an adhesive tape lined with
また、本発明の両面粘着テープの保持力のズレ距離は特に制限されるものではないが、2mm以下が好ましく、より好ましくは0.5mm以下、さらに好ましくは0.1mm以下である。保持力のズレ距離が上記に範囲にあることで、高温で使用した際も充分な凝集力があり、反発力によるハガレや部品又は芯材の収縮を抑制することができる。保持力はJISZ0237に準じて測定される。具体的にはステンレス板(ヘアライン)にアルミ箔50μmで裏打ちした粘着テープを貼り合せ、2kgローラーで1往復加圧し、23℃50%RHの条件下で1時間放置する。さらに100℃で100gの荷重を鉛直方向にかけ、24時間後のズレ距離をノギスで測定する。 Moreover, although the shift | offset | difference distance of the holding force of the double-sided adhesive tape of this invention is not restrict | limited in particular, 2 mm or less is preferable, More preferably, it is 0.5 mm or less, More preferably, it is 0.1 mm or less. When the shift distance of the holding force is in the above range, there is sufficient cohesive force even when used at a high temperature, and it is possible to suppress the peeling or contraction of the component or the core material due to the repulsive force. Holding power is measured according to JISZ0237. Specifically, an adhesive tape lined with 50 μm aluminum foil is bonded to a stainless steel plate (hairline), pressed once with a 2 kg roller, and left at 23 ° C. and 50% RH for 1 hour. Further, a load of 100 g is applied in the vertical direction at 100 ° C., and the deviation distance after 24 hours is measured with a caliper.
本発明の両面粘着テープの破断強度は、特に限定されるものではないが、30MPa〜200MPaが好ましく、さらに好ましくは40MPa〜120MPaである。破断強度は次の方法で測定できる。両面粘着テープを10mm幅に切断し、その表面に50mm間隔の標点をつけて試験片(10mm幅)を作製し、引張試験機を使用し、室温(23℃)で且つ65%RHの条件下、試験片のつかみ間隔(チャック間距離)50mm、引張速度200mm/minの条件で、試験片を引っ張り、試験片が破断した時点(少なくとも一部より亀裂が生じた時点)の荷重(応力)を測定し、該荷重を破断強度(MPa)とする。 The breaking strength of the double-sided pressure-sensitive adhesive tape of the present invention is not particularly limited, but is preferably 30 MPa to 200 MPa, and more preferably 40 MPa to 120 MPa. The breaking strength can be measured by the following method. Cut the double-sided adhesive tape to 10mm width, make a test piece (10mm width) with marks on the surface at intervals of 50mm, use a tensile tester, room temperature (23 ° C) and 65% RH condition Below, the load (stress) at the time when the test piece was pulled and the test piece broke (at least when a crack occurred from a part) under the conditions of 50 mm of the test piece gripping distance (distance between chucks) and a pulling speed of 200 mm / min. And the load is taken as the breaking strength (MPa).
(支持体)
支持体の厚みは1μm〜3μmである。好ましくは1.5μm〜2.5μmである。上記範囲の厚みとすることで、薄型でありながら、必要充分な耐熱性や接着性を発現させることができる。
(Support)
The thickness of the support is 1 μm to 3 μm. Preferably they are 1.5 micrometers-2.5 micrometers. By setting it as the thickness of the said range, necessary and sufficient heat resistance and adhesiveness can be expressed, although it is thin.
支持体の動摩擦係数は0.20〜0.28である。さらに好ましくは0.22〜0.26である。上記範囲にあることで、適度な滑り性が支持体にあり、薄膜であってもシワが入りにくく、粘着テープの生産性に優れる。支持体の動摩擦係数は下記方法で測定する。 The dynamic friction coefficient of the support is 0.20 to 0.28. More preferably, it is 0.22-0.26. By being in the said range, moderate slipperiness exists in a support body, even if it is a thin film, it is hard to wrinkle and it is excellent in productivity of an adhesive tape. The dynamic friction coefficient of the support is measured by the following method.
(支持体の動摩擦係数)
JISK7125に準じ、SUS鏡面とフィルム面の摩擦係数を測定する。図4のように裏打ち用片面粘着テープ「DIC製 PET50SER」21で裏打ちしたフィルム22を貼り、63mm×63mmのすべり片(重さ:1.96N)23と片面粘着テープ21が接するように固定する。次にそのすべり片に固定したフィルム22がSUS鏡面25と接するように置き、100mm/minですべり片23をロードセル26で引っ張り測定した。動摩擦係数は次式で算出する。
動摩擦係数[−]=動摩擦力[N]/1.96[N]
(Dynamic friction coefficient of support)
According to JISK7125, the friction coefficient between the SUS mirror surface and the film surface is measured. As shown in FIG. 4, a
Coefficient of dynamic friction [−] = Dynamic friction force [N] /1.96 [N]
本発明においては、上記動摩擦係数を有する支持体を適宜選択して使用すればよく、また、支持体の動摩擦係数は微量の無機粒子を添加する等の手法により制御することができる。このような無機粒子としては、例えば、シリカ、炭酸カルシウム、炭酸マグネシウム、炭酸バリウム、硫酸カルシウム、リン酸カルシウム、リン酸マグネシウム、酸化ケイ素、カオリン、酸化アルミニウム等の粒子を添加することが好ましい。 In the present invention, a support having the above dynamic friction coefficient may be appropriately selected and used, and the dynamic friction coefficient of the support can be controlled by a technique such as adding a trace amount of inorganic particles. As such inorganic particles, for example, particles such as silica, calcium carbonate, magnesium carbonate, barium carbonate, calcium sulfate, calcium phosphate, magnesium phosphate, silicon oxide, kaolin, and aluminum oxide are preferably added.
粒子の平均粒径は特に限定されるものではないが、0.1μm〜3μmが好ましい。その中でも0.2μm〜2.5μmが好ましい。該範囲とすることで、動摩擦係数を上記範囲に調整しやすく、テープ製造時のシワの発生を好適に抑制しやすくなる。また、当該範囲とすることで支持体の凹凸が大きくなりすぎず、ラミネート時に粘着剤層を追従させやすく、高温環境下での熱収縮の抑制にも貢献しやすくなる。 Although the average particle diameter of particle | grains is not specifically limited, 0.1 micrometer-3 micrometers are preferable. Among these, 0.2 μm to 2.5 μm is preferable. By setting it as this range, it becomes easy to adjust a dynamic friction coefficient to the said range, and it becomes easy to suppress suitably the generation | occurrence | production of the wrinkle at the time of tape manufacture. Moreover, by setting it as the said range, the unevenness | corrugation of a support body does not become large too much, it is easy to follow an adhesive layer at the time of lamination, and it becomes easy to contribute also to suppression of the heat shrink in a high temperature environment.
これら粒子の含有量は、特に限定されるものではないが、0.01〜1質量%であることが好ましい。より好ましくは0.02〜0.5質量%である。少なすぎると動摩擦力が大きくなり、多すぎると動摩擦力が小さくなりすぎる。 The content of these particles is not particularly limited, but is preferably 0.01 to 1% by mass. More preferably, it is 0.02-0.5 mass%. If the amount is too small, the dynamic friction force becomes large. If the amount is too large, the dynamic friction force becomes too small.
支持体の熱収縮率は3%以下である。より好ましくは2%以下であり、さらに好ましくは1%以下である。上記範囲にあることで、ラミネート時にフィルムに熱をかける場合に縮みが発生しにくく生産性に優れる。また、粘着テープとしての耐熱収縮性も高度に実現できる。支持体の熱収縮率は下記方法で測定する。 The thermal contraction rate of the support is 3% or less. More preferably, it is 2% or less, More preferably, it is 1% or less. By being in the above-mentioned range, when heat is applied to the film during lamination, shrinkage hardly occurs and the productivity is excellent. Moreover, the heat shrinkability as an adhesive tape can also be realized to a high degree. The thermal contraction rate of the support is measured by the following method.
JISC2151に従い次のとおり測定する。100mm×100mのフィルムを150℃の乾燥器に30分放置し、乾燥器に入れる前後でのサイズをノギスで測定し、算出する。
熱収縮率=100×(乾燥器に入れる前の長さ−乾燥器に入れた後の長さ)/乾燥器に入れる前の長さ
Measured as follows according to JISC2151. A 100 mm × 100 m film is allowed to stand in a dryer at 150 ° C. for 30 minutes, and the size before and after placing in the dryer is measured with a caliper and calculated.
Heat shrinkage rate = 100 × (length before being put in the dryer−length after being put in the dryer) / length before being put in the dryer
本発明においては、上記熱収縮率を有する支持体を適宜選択して使用すればよく、また、支持体の熱収縮率は熱固定等の手法により制御することができる。当該熱固定は、延伸後の樹脂フィルムに対し、160℃〜240℃で1秒〜600秒間の条件で行うことが好ましく、さらに好ましくは、170℃〜235℃、特に好ましくは、200〜230℃である。当該条件とすることで、支持体の熱収縮率を上記範囲に調整しやすく、また、支持体の耐加水分解性も向上させやすくなる。 In the present invention, a support having the above heat shrinkage may be appropriately selected and used, and the heat shrinkage of the support can be controlled by a technique such as heat fixation. The heat setting is preferably performed at 160 ° C. to 240 ° C. for 1 second to 600 seconds with respect to the stretched resin film, more preferably 170 ° C. to 235 ° C., and particularly preferably 200 to 230 ° C. It is. By setting it as the said conditions, it becomes easy to adjust the thermal contraction rate of a support body to the said range, and it becomes easy to improve the hydrolysis resistance of a support body.
上記厚み、動摩擦係数及び熱収縮率を有する支持体としては、例えば、三菱樹脂製K100−2.0WやK583−2.5Wがあげられる。 Examples of the support having the thickness, the dynamic friction coefficient, and the thermal contraction rate include K100-2.0W and K583-2.5W manufactured by Mitsubishi Plastics.
使用する支持体としては、上記特性を有するものであれば各種材質のものを使用でき、なかでも合成樹脂フィルムを好適に用いることができる。具体的には、例えば、ポリエチレンテレフタレート(PET)、ポリエチレンナフタレート(PEN)、ポリブチレンテレフタレート(PBT)等のポリエステル、ポリアミド(ナイロン)、全芳香族ポリアミド(アラミド)等のアミド系樹脂、ポリブチルアクリレート、ポリエチルアクリレート等のポリアクリレート系樹脂、メチルメタクリレート(PMMA)等のメタクリレート系樹脂、ポリスチレン、アクリロニトリル−スチレン共重合体(AS樹脂)、アクリロニトリル−ブタジエン−スチレン共重合体(ABS樹脂)等のスチレン系樹脂、ポリエーテルエーテルケトン(PEEK)、ポリエーテルケトンケトン等のポリエーテルケトン類、さらには、ポリエーテルスルホン(PES)、ポリスルホン、ポリ塩化ビニル(PVC)、ポリフェニレンスルフィド(PPS)、ポリイミド(PI)、ポリアミドイミド、ポリエーテルイミド(PEI)、ポリエステルイミド、ポリカーボネート(PC)、ポリアセタール、ポリアリーレンエーテル(ポリフェニレンエーテルなど)、ポリフェニレンスルフィド、ポリアリレート、ポリアリール、ポリウレタン類、エポキシ系樹脂などが挙げられる。これらの素材(プラスチック材)は単独で又は2種以上組み合わせて使用することができる。 As a support to be used, various materials can be used as long as they have the above characteristics, and among them, a synthetic resin film can be suitably used. Specifically, for example, polyesters such as polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), amide resins such as polyamide (nylon) and wholly aromatic polyamide (aramid), polybutyl Polyacrylate resins such as acrylate and polyethyl acrylate, methacrylate resins such as methyl methacrylate (PMMA), polystyrene, acrylonitrile-styrene copolymer (AS resin), acrylonitrile-butadiene-styrene copolymer (ABS resin), etc. Polystyrene ketones such as styrene resins, polyether ether ketone (PEEK), and polyether ketone ketone, as well as polyether sulfone (PES), polysulfone, polyvinyl chloride (PVC), Rephenylene sulfide (PPS), polyimide (PI), polyamideimide, polyetherimide (PEI), polyesterimide, polycarbonate (PC), polyacetal, polyarylene ether (polyphenylene ether, etc.), polyphenylene sulfide, polyarylate, polyaryl, polyurethane And epoxy resins. These materials (plastic materials) can be used alone or in combination of two or more.
これらのなかでも、厚さ精度、経済性(コスト)、引張強度や加工性等の観点より、ポリエステルフィルムを好適に使用でき、ポリエチレンテレフタレートフィルムを特に好適に用いることができる。また、ポリエステルフィルムは二軸延伸したフィルムが好ましい。二軸延伸することで、高い強度を発現できる。 Among these, from the viewpoints of thickness accuracy, economy (cost), tensile strength, workability, and the like, a polyester film can be preferably used, and a polyethylene terephthalate film can be particularly preferably used. The polyester film is preferably a biaxially stretched film. High strength can be expressed by biaxial stretching.
以下、ポリエステルフィルムの製造方法に関して具体的に説明する。公知の手法により乾燥したまたは未乾燥のポリエステルチップ(ポリエステル成分)を必要に応じ着色顔料、あるいは着色顔料を高濃度に含むマスターバッチとを混練押出機に供給し、ポリエステル成分の融点以上である温度に加熱し溶融する。次いで、溶融したポリエステルをダイから押出し、回転冷却ドラム上でガラス転移温度以下の温度になるように急冷固化し、実質的に非晶状態の未配向シートを得る。この場合、シートの平面性を向上させるため、シートと回転冷却ドラムとの密着性を高めることが好ましく静電印加密着法および/または液体塗布密着法が好ましく採用される。溶融押出工程においても、押出機内でのポリエステルの滞留時間を短くすること、一軸押出機を使用する場合は原料をあらかじめ水分量が50ppm以下、好ましくは30ppm以下になるように十分乾燥すること、二軸押出機を使用する場合はベント口を設け、40ヘクトパスカル以下、好ましくは30ヘクトパスカル以下、さらに好ましくは20ヘクトパスカル以下の減圧を維持すること等の方法を採用する。 Hereinafter, the manufacturing method of a polyester film is demonstrated concretely. A polyester chip (polyester component) dried or undried by a known method is supplied to a kneading extruder with a coloring pigment or a master batch containing a high concentration of the coloring pigment as necessary, and a temperature equal to or higher than the melting point of the polyester component. Heat to melt. Next, the melted polyester is extruded from a die, and rapidly cooled and solidified on a rotary cooling drum so that the temperature is equal to or lower than the glass transition temperature, thereby obtaining a substantially amorphous unoriented sheet. In this case, in order to improve the flatness of the sheet, it is preferable to improve the adhesion between the sheet and the rotary cooling drum, and an electrostatic application adhesion method and / or a liquid application adhesion method are preferably employed. Also in the melt-extrusion step, shorten the residence time of the polyester in the extruder, and when using a single screw extruder, dry the raw material in advance so that the moisture content is 50 ppm or less, preferably 30 ppm or less. When a shaft extruder is used, a method is adopted in which a vent port is provided and a reduced pressure of 40 hectopascals or less, preferably 30 hectopascals or less, more preferably 20 hectopascals or less is maintained.
このようにして得られたシートを2軸方向に延伸してフィルム化する。延伸条件について具体的に述べると、前記未延伸シートを好ましくは縦方向に70〜145℃で2〜6倍に延伸し、縦1軸延伸フィルムとした後、横方向に90〜160℃で2〜6倍延伸を行い、熱固定工程に移る。さらにこの際、熱処理の最高温度ゾーンおよび/または熱処理出口のクーリングゾーンにおいて、縦方向および/または横方向に0.1〜20%弛緩する方法が好ましい。また、必要に応じて再縦延伸、再横延伸を付加することも可能である。 The sheet thus obtained is stretched in the biaxial direction to form a film. Specifically describing the stretching conditions, the unstretched sheet is preferably stretched 2 to 6 times at 70 to 145 ° C. in the longitudinal direction to form a longitudinal uniaxially stretched film, and then 2 to 90 to 160 ° C. in the lateral direction. Perform ~ 6 times stretching and move to heat setting step. Further, at this time, a method of relaxing 0.1 to 20% in the longitudinal direction and / or the transverse direction in the maximum temperature zone of the heat treatment and / or the cooling zone at the heat treatment outlet is preferable. Further, it is possible to add re-longitudinal stretching and re-lateral stretching as necessary.
なお、支持体は、単層、積層のいずれの形態を有していてもよく、構造上の制約を受けない。 The support may have any form of a single layer or a laminate, and is not subject to structural restrictions.
なお、支持体(特に、プラスチック材による支持体)の表面は、支持体上に形成される粘着剤層などとの密着性を高めるため、慣用の表面処理、例えば、クロム酸処理、オゾン暴露、火炎暴露、高圧電撃暴露、イオン化放射線処理等の化学的又は物理的方法による酸化処理等が施されていてもよく、下塗り剤によるコーティング処理等が施されていてもよい。 The surface of the support (particularly, a support made of a plastic material) has a conventional surface treatment, for example, chromic acid treatment, ozone exposure, etc., in order to enhance the adhesion with the pressure-sensitive adhesive layer formed on the support. Oxidation treatment by a chemical or physical method such as flame exposure, high-voltage impact exposure, ionizing radiation treatment, or the like may be performed, or a coating treatment with a primer may be performed.
(粘着剤層)
本発明の両面粘着テープの粘着剤層を形成する粘着剤としては、特に制限されず、例えば、アクリル系粘着剤、ゴム系粘着剤、シリコーン系粘着剤、ウレタン系粘着剤、ポリエステル系粘着剤、スチレン−ジエンブロック共重合体系粘着剤、ビニルアルキルエーテル系粘着剤、ポリアミド系粘着剤、フッ素系粘着剤、クリ−プ特性改良型粘着剤、放射線硬化型粘着剤などの公知の粘着剤から適宜選択して用いることができる。粘着剤は単独で又は2種以上組み合わせて使用することができる。
(Adhesive layer)
The pressure-sensitive adhesive forming the pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape of the present invention is not particularly limited. For example, an acrylic pressure-sensitive adhesive, a rubber-based pressure-sensitive adhesive, a silicone-based pressure-sensitive adhesive, a urethane-based pressure-sensitive adhesive, a polyester-based pressure-sensitive adhesive, Appropriately selected from known adhesives such as styrene-diene block copolymer adhesives, vinyl alkyl ether adhesives, polyamide adhesives, fluorine adhesives, improved creep characteristics adhesives, and radiation curable adhesives. Can be used. An adhesive can be used individually or in combination of 2 or more types.
粘着剤としては、特にアクリル系粘着剤が、接着信頼性が高いことから好適に用いることができる。アクリル系粘着剤は、アクリル系ポリマーを粘着性成分又は主剤とし、これに必要に応じて、架橋剤、粘着付与剤、軟化剤、可塑剤、充填剤、老化防止剤、着色剤などの適宜な添加剤が含まれている。アクリル系ポリマーは、(メタ)アクリル酸アルキルエステルを単量体主成分とするポリマーであり、必要に応じて(メタ)アルキルエステルに対して共重合が可能な単量体(共重合性単量体)を用いることにより調製されている。(メタ)アクリル酸アルキルエステルとしては、例えば、(メタ)アクリル酸メチル、(メタ)アクリル酸エチル、(メタ)アクリル酸プロピル、(メタ)アクリル酸イソプロピル、(メタ)アクリル酸ブチル、(メタ)アクリル酸イソブチル、(メタ)アクリル酸s−ブチル、(メタ)アクリル酸t−ブチル、(メタ)アクリル酸ペンチル、(メタ)アクリル酸ヘキシル、(メタ)アクリル酸ヘプチル、(メタ)アクリル酸オクチル、(メタ)アクリル酸2−エチルヘキシル、(メタ)アクリル酸イソオクチル、(メタ)アクリル酸ノニル、(メタ)アクリル酸イソノニル、(メタ)アクリル酸デシル、(メタ)アクリル酸イソデシル、(メタ)アクリル酸ウンデシル、(メタ)アクリル酸ドデシル、(メタ)アクリル酸トリデシル、(メタ)アクリル酸テトラデシル、(メタ)アクリル酸ペンタデシル、(メタ)アクリル酸ヘキサデシル、(メタ)アクリル酸ヘプタデシル、(メタ)アクリル酸オクタデシル、(メタ)アクリル酸ノナデシル、(メタ)アクリル酸エイコシルなどの(メタ)アクリル酸C1−20アルキルエステル[好ましくは(メタ)アクリル酸C4−18アルキル(直鎖状又は分岐鎖状のアルキル)エステル]などが挙げられる。(メタ)アクリル酸アルキルエステルは、目的とする粘着性などに応じて適宜選択することができる。(メタ)アクリル酸アルキルエステルは単独で又は2種以上組み合わせて使用することができる。 As the pressure-sensitive adhesive, an acrylic pressure-sensitive adhesive can be preferably used because it has high adhesion reliability. The acrylic pressure-sensitive adhesive has an acrylic polymer as a pressure-sensitive adhesive component or main ingredient and, as necessary, an appropriate agent such as a crosslinking agent, a tackifier, a softener, a plasticizer, a filler, an anti-aging agent, or a colorant. Additives are included. Acrylic polymer is a polymer that has (meth) acrylic acid alkyl ester as the main component of monomer and can be copolymerized with (meth) alkyl ester as needed (copolymerizable monomer) Body). Examples of the (meth) acrylic acid alkyl ester include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, isopropyl (meth) acrylate, butyl (meth) acrylate, (meth) Isobutyl acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, 2-Methylhexyl acrylate, isooctyl (meth) acrylate, nonyl (meth) acrylate, isononyl (meth) acrylate, decyl (meth) acrylate, isodecyl (meth) acrylate, undecyl (meth) acrylate , Dodecyl (meth) acrylate, tridecyl (meth) acrylate, (me ) Tetradecyl acrylate, pentadecyl (meth) acrylate, hexadecyl (meth) acrylate, heptadecyl (meth) acrylate, octadecyl (meth) acrylate, nonadecyl (meth) acrylate, eicosyl (meth) acrylate (meta) ) Acrylic acid C1-20 alkyl ester [preferably (meth) acrylic acid C4-18 alkyl (straight or branched alkyl) ester] and the like. The (meth) acrylic acid alkyl ester can be appropriately selected according to the intended tackiness and the like. The (meth) acrylic acid alkyl ester can be used alone or in combination of two or more.
また、前記(メタ)アルキルエステルに対して共重合可能な共重合性単量体としては、例えば、(メタ)アクリル酸、イタコン酸、マレイン酸、フマル酸、クロトン酸、イソクロトン酸などのカルボキシル基含有単量体又はその無水物;ビニルスルホン酸ナトリウムなどのスルホン酸基含有単量体;スチレン、置換スチレンなどの芳香族ビニル化合物;アクリロニトリルなどのシアノ基含有単量体;エチレン、プロピレン、ブタジエンなどのオレフィン類;酢酸ビニルなどのビニルエステル類;塩化ビニル;アクリルアミド、メタアクリルアミド、N−ビニルピロリドン、N,N−ジメチル(メタ)アクリルアミドなどのアミド基含有単量体;(メタ)アクリル酸ヒドロキシアルキル、グリセリンジメタクリレートなどのヒドロキシル基含有単量体;(メタ)アクリル酸アミノエチル、(メタ)アクリロイルモルホリンなどのアミノ基含有単量体;シクロヘキシルマレイミド、イソプロピルマレイミドなどのイミド基含有単量体;(メタ)アクリル酸グリシジル、(メタ)アクリル酸メチルグリシジルなどのエポキシ基含有単量体;2−メタクリロイルオキシエチルイソシアネートなどのイソシアネート基含有単量体の他、トリエチレングリコールジ(メタ)アクリレート、ジエチレングリコールジ(メタ)アクリレート、エチレングリコールジ(メタ)アクリレート、テトラエチレングリコールジ(メタ)アクリレート、ネオペンチルグリコールジ(メタ)アクリレート、1,6−ヘキサンジオールジ(メタ)アクリレート、トリメチロールプロパントリ(メタ)アクリレート、ペンタエリスリトールトリ(メタ)アクリレート、ジペンタエリスリトールヘキサ(メタ)アクリレート、ジビニルベンゼンなどの多官能性の共重合性単量体(多官能モノマー)などが挙げられる。共重合性単量体は単独で又は2種以上組み合わせて使用することができる。共重合性単量体としては、カルボキシル基などの官能基を有する改質用モノマーを好適に用いることができる。 Examples of the copolymerizable monomer copolymerizable with the (meth) alkyl ester include carboxyl groups such as (meth) acrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, and isocrotonic acid. -Containing monomers or anhydrides thereof; sulfonic acid group-containing monomers such as sodium vinyl sulfonate; aromatic vinyl compounds such as styrene and substituted styrene; cyano group-containing monomers such as acrylonitrile; ethylene, propylene, butadiene, etc. Olefins; vinyl esters such as vinyl acetate; vinyl chloride; amide group-containing monomers such as acrylamide, methacrylamide, N-vinylpyrrolidone, N, N-dimethyl (meth) acrylamide; hydroxyalkyl (meth) acrylate Contains hydroxyl groups such as glycerin dimethacrylate Monomers; amino group-containing monomers such as aminoethyl (meth) acrylate and (meth) acryloylmorpholine; imide group-containing monomers such as cyclohexylmaleimide and isopropylmaleimide; glycidyl (meth) acrylate and (meth) acrylic Epoxy group-containing monomers such as methyl glycidyl acid; isocyanate group-containing monomers such as 2-methacryloyloxyethyl isocyanate, triethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, ethylene glycol di (meta ) Acrylate, tetraethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, Pentaerythritol tri (meth) acrylate, dipentaerythritol hexa (meth) acrylate, a polyfunctional copolymerizable monomer (polyfunctional monomer) such as divinylbenzene, and the like. A copolymerizable monomer can be used individually or in combination of 2 or more types. As the copolymerizable monomer, a modifying monomer having a functional group such as a carboxyl group can be suitably used.
アクリル系ポリマーの質量平均分子量(Mw)は好ましくは50万〜120万である。さらに好ましくは70万〜120万である。最も好ましくは100万〜120万である。上記範囲にあることで、薄膜であっても充分な接着性・耐熱性を発現しやすい。分子量はGPCによってスチレン換算で測定される。 The mass average molecular weight (Mw) of the acrylic polymer is preferably 500,000 to 1,200,000. More preferably, it is 700,000 to 1,200,000. Most preferably, it is 1 million to 1.2 million. By being in the said range, even if it is a thin film, it is easy to express sufficient adhesiveness and heat resistance. The molecular weight is measured in terms of styrene by GPC.
本発明においては、粘着剤層の粘着力を向上させるため、粘着付与樹脂を添加することも好ましい。また、これら粘着付与樹脂を添加することで、引張強度や引張破断強度を高くすることができることから、使用するアクリル系共重合体に応じて、粘着付与樹脂を適宜添加することで、引張強度や引張破断強度を調整できる。本発明の両面粘着テープの粘着剤層に添加する粘着付与樹脂としては、例えば、ロジンやロジンのエステル化合物等のロジン系樹脂;ジテルペン重合体やα−ピネン−フェノール共重合体等のテルペン系樹脂;脂肪族系(C5系)や芳香族系(C9)等の石油樹脂;その他、スチレン系樹脂、フェノール系樹脂、キシレン樹脂等が挙げられる。そのなかでもn−ブチル(メタ)アクリレートを主たるモノマー成分とするアクリル系共重合体を使用した粘着剤組成物においては、薄型で粘着力と耐熱性を両立させるに際し、ロジン系樹脂とスチレン系樹脂を混合して使用することが好ましい。 In the present invention, it is also preferable to add a tackifier resin in order to improve the adhesive strength of the adhesive layer. In addition, by adding these tackifying resins, it is possible to increase the tensile strength and tensile rupture strength, so depending on the acrylic copolymer used, by appropriately adding a tackifying resin, the tensile strength and The tensile breaking strength can be adjusted. Examples of the tackifying resin added to the pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape of the present invention include rosin resins such as rosin and rosin ester compounds; terpene resins such as diterpene polymers and α-pinene-phenol copolymers. A petroleum resin such as an aliphatic (C5) or aromatic (C9); a styrene resin, a phenol resin, a xylene resin, and the like. In particular, in a pressure-sensitive adhesive composition using an acrylic copolymer having n-butyl (meth) acrylate as a main monomer component, a rosin-based resin and a styrene-based resin are used to achieve a thin and compatible adhesive force and heat resistance. Are preferably used in combination.
また初期接着力を上げるため、常温で液状の粘着付与樹脂を混合して使用することが好ましい。常温で液状の粘着付与樹脂としては、例えば、前記した常温で固体の粘着付与樹脂の液状樹脂や、プロセスオイル、ポリエステル系可塑剤、ポリブテン等の低分子量の液状ゴムが挙げられる。特にテルペンフェノール樹脂が好ましい。市販品としてはヤスハラケミカル社製YP−90L等がある。液晶粘着付与樹脂の添加量はアクリル系共重合体100質量部に対して1〜20質量部を添加するのが好ましい。 In order to increase the initial adhesive force, it is preferable to mix and use a tackifying resin that is liquid at room temperature. Examples of the tackifying resin that is liquid at normal temperature include liquid resins of the above-described tackifying resin that is solid at normal temperature, and low molecular weight liquid rubbers such as process oil, polyester plasticizer, and polybutene. A terpene phenol resin is particularly preferable. Commercially available products include YP-90L manufactured by Yasuhara Chemical. The addition amount of the liquid crystal tackifying resin is preferably 1 to 20 parts by mass with respect to 100 parts by mass of the acrylic copolymer.
粘着付与樹脂の添加量としては、アクリル系共重合体100質量部に対して20〜60質量部を添加するのが好ましい。より好ましくは30〜50質量部である。粘着付与樹脂を添加することにより粘着力を向上させることができる。 As addition amount of tackifying resin, it is preferable to add 20-60 mass parts with respect to 100 mass parts of acrylic copolymers. More preferably, it is 30-50 mass parts. Adhesive strength can be improved by adding a tackifying resin.
粘着剤のゲル分率は特に制限されるものではないが、5〜50%であることが薄膜であっても充分な接着性・耐熱性を発現しやすいため好ましく、10〜30%であることがより好ましく、さらに好ましくは15〜25%である。ゲル分率は、養生後の粘着剤層をトルエン中に浸漬し、24時間放置後に残った不溶分の乾燥後の質量を測定し、元の質量に対する百分率で表す。
ゲル分率=[(粘着剤層のトルエン浸漬後質量)/(粘着剤層のトルエン浸漬前質量)]×100
The gel fraction of the pressure-sensitive adhesive is not particularly limited, but it is preferably 5 to 50% because it is easy to express sufficient adhesiveness and heat resistance even in a thin film, and is preferably 10 to 30%. Is more preferable, and further preferably 15 to 25%. The gel fraction is expressed as a percentage with respect to the original mass by immersing the cured adhesive layer in toluene, measuring the mass after drying of the insoluble matter left after standing for 24 hours, and measuring the mass.
Gel fraction = [(mass after pressure-sensitive adhesive layer is immersed in toluene) / (weight of pressure-sensitive adhesive layer before immersion in toluene)] × 100
アクリル系ポリマーは、溶液重合法、エマルション重合法、紫外線照射重合法等の慣用の重合方法により調製することができる。 The acrylic polymer can be prepared by a conventional polymerization method such as a solution polymerization method, an emulsion polymerization method, or an ultraviolet irradiation polymerization method.
各粘着剤層の厚みとしては、特に制限されないが、0.5μm〜4μmが好ましく、さらに好ましくは1μm〜3μmである。上記範囲にあることで薄さと粘着物性を両立しやすい。特に0.5μm未満である場合は、接着力が著しく低下する。また、支持体の両面に形成された2つの粘着剤層の厚みは、同一であっても、異なっていてもよい。 Although it does not restrict | limit especially as thickness of each adhesive layer, 0.5 micrometer-4 micrometers are preferable, More preferably, they are 1 micrometer-3 micrometers. It exists in the said range and it is easy to make thinness and adhesive physical property compatible. In particular, when it is less than 0.5 μm, the adhesive strength is remarkably reduced. Moreover, the thickness of the two adhesive layers formed on both surfaces of the support may be the same or different.
(剥離ライナー)
本発明の両面粘着テープは、粘着剤層を保護するために、各粘着剤層表面に剥離ライナーが設けられていても良い。当該剥離ライナーとしては、公知の剥離ライナーを適宜選択して使用すればよく、例えば、ポリエチレン、ポリプロピレン、エチレン−プロピレン共重合体等のエチレン−α−オレフィン共重合体や、これらの混合物からなるポリオレフィン系樹脂等の各種樹脂フィルムからなる剥離ライナーを好ましく使用でき、これら樹脂フィルムは発泡形状のものであってもよい。また、樹脂フィルム以外にも、和紙、洋紙、グラシン紙等の紙、不織布、金属箔等も使用できる。さらには、これらが積層された複合シートであってもよい。
(Release liner)
In the double-sided pressure-sensitive adhesive tape of the present invention, a release liner may be provided on the surface of each pressure-sensitive adhesive layer in order to protect the pressure-sensitive adhesive layer. As the release liner, a known release liner may be appropriately selected and used, for example, an ethylene-α-olefin copolymer such as polyethylene, polypropylene, ethylene-propylene copolymer, or a polyolefin composed of a mixture thereof. A release liner made of various resin films such as resin can be preferably used, and these resin films may be foamed. In addition to the resin film, paper such as Japanese paper, western paper, glassine paper, non-woven fabric, metal foil, and the like can also be used. Furthermore, a composite sheet in which these are laminated may be used.
これら剥離ライナーの表面は、易剥離性を付与するために剥離処理層が設けられていることが好ましい。剥離処理層としては、両面粘着テープの剥離ライナー用に使用される各種の剥離処理剤により形成することができ、このような剥離処理剤としては、例えば、シリコーン系、フッ素系、長鎖アルキル系剥離処理剤等を好ましく使用できる。また、剥離処理層は、上記の樹脂フィルム上に、ラミネートやコーティングにより形成されていてもよい。 The surface of these release liners is preferably provided with a release treatment layer in order to impart easy peelability. The release treatment layer can be formed of various release treatment agents used for release liners for double-sided pressure-sensitive adhesive tapes. Examples of such release treatment agents include silicone-based, fluorine-based, and long-chain alkyl-based agents. A release treatment agent or the like can be preferably used. The release treatment layer may be formed on the above resin film by lamination or coating.
剥離ライナーの剥離力は、使用態様等に応じて適宜調整すればよいが、粘着剤層に対する剥離力が0.01〜2N/20mm、好ましくは0.05〜0.15N/20mmとすることで、剥離ライナーを剥離する際に、両面粘着テープの変形を抑制しやすくなるため好ましい。剥離力は剥離ライナー又は50μm厚さのPET裏打ちした粘着剤層を0.3〜10m/minの速度で180°方向に剥離して測定できる。 The release force of the release liner may be appropriately adjusted according to the use mode and the like, but the release force for the pressure-sensitive adhesive layer is 0.01 to 2 N / 20 mm, preferably 0.05 to 0.15 N / 20 mm. When peeling the release liner, it is preferable because deformation of the double-sided pressure-sensitive adhesive tape is easily suppressed. The peeling force can be measured by peeling a release liner or a 50 μm thick PET-backed pressure-sensitive adhesive layer in a 180 ° direction at a speed of 0.3 to 10 m / min.
(製造方法)
本発明の両面粘着テープは、公知の製造方法により製造でき、例えば、支持体の一面に粘着剤を塗布して、第1の粘着剤層を形成した後、又は第1の粘着剤層の形成とともに、支持体の他方の面に粘着剤を塗布して、第2の粘着剤層を形成する製造方法や、剥離ライナーに粘着剤を塗布して粘着剤層付きの剥離ライナーを形成し、これを支持体の両面に貼り合わせる製造方法等があげられる。
特に、本発明においては、下記の工程(A1)(B1)(A2)(B2)を具備する両面粘着テープの製造方法などが好ましく挙げられる。
工程(A1):剥離ライナーの剥離処理面に、粘着剤を塗布して剥離ライナー上に粘着剤層を形成する工程
工程(B1):支持体の一方の表面に、剥離ライナー上に形成された粘着剤層を貼り合わせて、支持体上に第1の粘着剤層を形成する工程
工程(A2):もう一方の剥離ライナーの剥離処理面に、粘着剤を塗布して剥離ライナー上に粘着剤を形成する工程
工程(B2):粘着剤層、剥離ライナー付きの支持体のもう一方の支持体表面に、剥離ライナー上に形成された粘着剤層を貼り合せて、第2の粘着剤層を形成する工程
(Production method)
The double-sided pressure-sensitive adhesive tape of the present invention can be produced by a known production method. For example, after the pressure-sensitive adhesive is applied to one surface of the support to form the first pressure-sensitive adhesive layer, or the first pressure-sensitive adhesive layer is formed. In addition, a manufacturing method in which a second pressure-sensitive adhesive layer is formed by applying a pressure-sensitive adhesive to the other surface of the support, or a pressure-sensitive adhesive is applied to the release liner to form a release liner with a pressure-sensitive adhesive layer. The manufacturing method etc. which stick together to both surfaces of a support are mention | raise | lifted.
In particular, in the present invention, a method for producing a double-sided pressure-sensitive adhesive tape comprising the following steps (A1), (B1), (A2), and (B2) is preferred.
Step (A1): A step of applying a pressure-sensitive adhesive to the release treatment surface of the release liner to form a pressure-sensitive adhesive layer on the release liner. Step (B1): formed on the release liner on one surface of the support. A step of forming a first pressure-sensitive adhesive layer on the support by laminating the pressure-sensitive adhesive layer Step (A2): A pressure-sensitive adhesive is applied to the release treatment surface of the other release liner, and the pressure-sensitive adhesive is formed on the release liner. Step (B2): The second pressure-sensitive adhesive layer is formed by laminating the pressure-sensitive adhesive layer formed on the release liner on the other surface of the pressure-sensitive adhesive layer and the support with the release liner. Forming process
当該工程を有する製造方法の概略図を図2〜3に示す。図2〜3の製造方法においては、剥離ライナー11の剥離処理面に、粘着剤塗工装置12により粘着剤を塗布し、乾燥及び/又は紫外線照射装置13にて粘着剤を乾燥及び/又は硬化させて、粘着剤層付き剥離ライナーが得られる(工程(A1))。得られた粘着剤層付き剥離ライナーの粘着剤層と支持体14とをラミネートロール15を通じて貼り合わせて、支持体/粘着剤層/剥離ライナーが積層された片面粘着テープ16が得られる(工程(B1))。次いで、他の剥離ライナー17の剥離処理面に、粘着剤塗工装置12により粘着剤を塗布し、乾燥及び/又は紫外線照射装置13にて粘着剤を乾燥及び/又は硬化させて、粘着剤層付き剥離ライナーを得た後(工程(A2))、当該粘着剤層付き剥離ライナーの粘着剤層と、工程(B1)を経て得られた支持体/粘着剤層/剥離ライナーが積層された片面粘着テープ16の支持体表面とを、ラミネートロール15を通じて貼り合わせて、支持体の両面に粘着剤層を有する両面粘着テープ18が得られる。当該製造方法においては、剥離ライナー11及び17、支持体14、片面粘着テープ16、両面粘着テープ18は、それぞれロール状から繰り出すか、ロール状に巻回されることが製造工程上有利であるため好ましい。
The schematic of the manufacturing method which has the said process is shown to FIGS. In the manufacturing method of FIGS. 2 to 3, an adhesive is applied to the release treatment surface of the
本発明の両面粘着テープは、支持体の片面に、剥離ライナー上に形成された粘着剤層を貼り合わせて、支持体上に第1の粘着剤層を形成する際に、支持体にかかる張力を実質0にしなくても通常の張力範囲で、支持体の厚みが非常に薄くても、シワ等を生じさせず、良好な状態で両面粘着テープを製造することができる。 The double-sided pressure-sensitive adhesive tape of the present invention has a tension applied to a support when a pressure-sensitive adhesive layer formed on a release liner is bonded to one side of the support to form a first pressure-sensitive adhesive layer on the support. Even if the thickness of the support is very thin, the double-sided pressure-sensitive adhesive tape can be produced in a good state without causing wrinkles or the like even if the thickness of the support is very thin.
従って、本発明の両面粘着テープとしては、図2〜3で示されるように、工程(A1)、工程(B1)、工程(A2)および工程(B2)を具備する製造方法により好適に作製することができる。特に、これらを具備する製造方法を用いることにより、シワ等を生じさせず、安定して、ロール状に巻回された形態の両面粘着テープ又はシートを製造することができる。 Therefore, as shown in FIGS. 2 to 3, the double-sided pressure-sensitive adhesive tape of the present invention is preferably produced by a production method comprising the step (A1), the step (B1), the step (A2) and the step (B2). be able to. In particular, by using a production method comprising these, it is possible to produce a double-sided pressure-sensitive adhesive tape or sheet that is stably wound into a roll without causing wrinkles or the like.
剥離ライナー上の粘着剤とフィルムを貼り合わせる工程では熱をかけてラミネートすること(熱ラミ)が好ましい。温度は40℃〜80℃が好ましい。熱をかけることによって、薄い粘着剤層であっても、すべり性の良い微細な凹凸があるフィルムの凹凸に追従しやすくなる。温度が低すぎると粘着剤とフィルムの密着性が低下し、温度が高すぎるとシワが発生する。本発明の粘着テープはフィルムが低い熱収縮率をもつため、熱をかけた際にも縮みによるシワが発生しにくく、生産性に優れる。 In the step of bonding the adhesive on the release liner and the film, it is preferable to laminate by applying heat (thermal lamination). The temperature is preferably 40 ° C to 80 ° C. By applying heat, even a thin pressure-sensitive adhesive layer can easily follow the unevenness of a film having fine unevenness with good sliding properties. When the temperature is too low, the adhesiveness between the pressure-sensitive adhesive and the film is lowered, and when the temperature is too high, wrinkles are generated. In the pressure-sensitive adhesive tape of the present invention, since the film has a low heat shrinkage rate, wrinkles due to shrinkage hardly occur even when heat is applied, and the productivity is excellent.
通常、3μm以下の薄い支持体を用いる場合は、製造時の支持体の張力を極めて低い状態(ほぼ0)にしないと、支持体と粘着テープを貼り合せる際に、支持体にシワ等がはいり易い。また支持体の張力をそのように調整するのは難しい。しかし本発明においては、特定の摩擦係数を有する支持体を用いているため、特段の製造シワ等を生じさせず、良好な状態でロール状に巻回された形態の両面粘着テープを安定して製造することができる。本発明に使用する支持体であれば、10〜300N/mの張力をかけることができる。そのなかでも30〜120N/mの張力が好ましい。 Normally, when a thin support of 3 μm or less is used, the support is not wrinkled when the support and the adhesive tape are bonded unless the tension of the support at the time of manufacture is extremely low (approximately 0). easy. Also, it is difficult to adjust the tension of the support in that way. However, in the present invention, since a support having a specific coefficient of friction is used, a double-sided pressure-sensitive adhesive tape wound in a roll state in a good state can be stably produced without causing special production wrinkles or the like. Can be manufactured. If it is a support body used for this invention, the tension | tensile_strength of 10-300 N / m can be applied. Of these, a tension of 30 to 120 N / m is preferable.
本発明の両面粘着テープを、ロール状に巻回された形態の両面粘着テープとして得る場合には、その長さは、長尺帯状の長さであれば特に制限されないが、通常、5m以上(好ましくは10m以上、さらに好ましくは20m以上)である。両面粘着テープを巻回された形態且つ長尺とした場合には、両面粘着テープを前もって部品の形状に切断加工する場合や、シーリング加工、プレス加工する場合等の作業性が良好となる。 When the double-sided pressure-sensitive adhesive tape of the present invention is obtained as a double-sided pressure-sensitive adhesive tape wound in a roll shape, the length is not particularly limited as long as it is a long belt-like length, but usually 5 m or more ( Preferably it is 10 m or more, more preferably 20 m or more. When the double-sided pressure-sensitive adhesive tape is wound and long, workability such as when the double-sided pressure-sensitive adhesive tape is cut into parts in advance, sealing, or pressing is improved.
本発明の両面粘着テープは、薄層化を要求されている接合部材、特に、接合部品間のクリアランスが従来両面粘着テープによる接合がなされていなかったような極狭小な場合(例えば、クリアランスが10μm以下の領域)での部品間の接合に好適に適用できる。なかでも、使用時に熱を発生するパソコン、デジタルカメラ、デジタルビデオカメラ等のOA機器や、電子手帳、携帯電話、PHS、スマートフォン、ゲーム機器、電子書籍等の携帯電子端末等の部品固定用途、例えばLCDモジュール、バックライトユニット、反射、遮光、放熱、磁性シート等の部品固定用途に好適に使用できる。特に、本発明の両面粘着テープは、極めて薄型でありながら耐熱性が良好であるため、使用により熱を発生する電子部品に貼り付けられる放熱シートや、磁性シートの固定に特に好適に使用できる。また、本発明の両面粘着テープは、このような極狭小なクリアランスに適用できる耐熱性に優れた薄型のテープでありながら、製造に際して支持体にかける張力を低くするといった特別な製造方法を使用しなくとも、シワの発生等を生じることなく好適に製造できる。 The double-sided pressure-sensitive adhesive tape of the present invention is a joining member that is required to be thinned, particularly when the clearance between joining parts is extremely small as in the case where the conventional double-sided pressure-sensitive adhesive tape has not been joined (for example, the clearance is 10 μm). The present invention can be suitably applied to joining between parts in the following areas). In particular, for fixing parts such as OA devices such as personal computers, digital cameras and digital video cameras that generate heat during use, and electronic electronic notebooks, mobile phones, PHS, smartphones, game devices, electronic books and other portable electronic terminals, for example It can be suitably used for fixing components such as LCD modules, backlight units, reflection, light shielding, heat dissipation, and magnetic sheets. In particular, since the double-sided pressure-sensitive adhesive tape of the present invention is extremely thin and has good heat resistance, it can be particularly suitably used for fixing a heat-dissipating sheet or a magnetic sheet that is attached to an electronic component that generates heat when used. In addition, the double-sided pressure-sensitive adhesive tape of the present invention is a thin tape excellent in heat resistance that can be applied to such an extremely narrow clearance, but uses a special production method such as reducing the tension applied to the support during production. Even if it does not, it can manufacture suitably, without producing wrinkles etc.
(放熱シート固定用途での使用法)
放熱シートは局所的な高温部に設置することで、熱を電子機器の全面に放熱し、いわゆるホットスポットを解決する役目を持つ。放熱シートに使用するグラファイトシートは、人工グラファイトシートや天然グラファイトシートの2種類がある。人工グラファイトシートとしては、ポリイミドフィルムのような有機フィルムを高温の不活性ガス雰囲気中で熱分解して得られる熱分解グラファイトシートがある。また、天然グラファイトシートは、天然の黒鉛を酸処理した後、加熱膨張させた黒鉛粉末を加圧してシート状にしたものがある。放熱シートに使用するグラファイトシートは、皺が少ない方が、放熱性が良いため、皺の少ない人工グラファイトシートが好適に用いられる。放熱シートに使用するグラファイトシートの厚さは、10〜100μmであることが好ましく、15〜50μmであることが更に好ましい。厚さを当該範囲とすることで、薄型携帯電子端末機器に好適に用いられる。
(Usage for fixing heat dissipation sheet)
By installing the heat-dissipating sheet in a local high-temperature part, the heat-dissipating sheet dissipates heat to the entire surface of the electronic device, thereby solving a so-called hot spot. There are two types of graphite sheets used for the heat dissipation sheet: artificial graphite sheets and natural graphite sheets. As the artificial graphite sheet, there is a pyrolytic graphite sheet obtained by pyrolyzing an organic film such as a polyimide film in a high-temperature inert gas atmosphere. In addition, there is a natural graphite sheet in which natural graphite is acid-treated and then heated and expanded into graphite powder. As the graphite sheet used for the heat dissipation sheet, an artificial graphite sheet with less wrinkles is preferably used because heat dissipation is better when there are fewer wrinkles. The thickness of the graphite sheet used for the heat radiating sheet is preferably 10 to 100 μm, and more preferably 15 to 50 μm. By setting the thickness within this range, it can be suitably used for a thin portable electronic terminal device.
本発明の粘着テープで貼り合せることで、テープの熱抵抗を低減でき、厚み方向の熱伝導率を向上できるため、放熱性を向上できる。また薄型化も可能である。 By bonding with the adhesive tape of the present invention, the thermal resistance of the tape can be reduced and the thermal conductivity in the thickness direction can be improved, so that the heat dissipation can be improved. Thinning is also possible.
(磁性シート固定用途での使用法)
磁性シートは、電子機器の筐体内面や各種電子部品の外面など、電磁波を遮断したい箇所に貼着され、これにより、外来電磁波が電子機器内部へ透過するのを防止したり、電子機器の内部から外部へ電磁波が漏出するのを防止したりすることができる。磁性シートは、Ni系フェライト磁性体粉末、Mg系フェライト磁性体粉末、Mn系フェライト磁性体粉末、Ba系フェライト磁性体粉末、Sr系フェライト磁性体粉末、Fe−Si合金粉末、Fe−Ni合金粉末、Fe−Co合金粉末、Fe−Si−Al合金粉末、Fe−Si−Cr合金粉末、鉄粉末、Fe系アモルファス、Co系アモルファス、Fe基ナノ結晶体等からなるシートであり、厚みが厚いほうが磁性的性能を発揮しやすい。この固定に粘着テープが用いられるが、本発明の粘着テープで固定することで、磁性シートを厚くしても、複合体(磁性シートと粘着テープの貼り合せ品)として薄型化できる。
(Usage for fixing magnetic sheet)
The magnetic sheet is affixed to places where electromagnetic waves are to be blocked, such as the inner surface of the casing of electronic devices and the outer surfaces of various electronic components, thereby preventing external electromagnetic waves from penetrating into the electronic device or inside the electronic device. It is possible to prevent electromagnetic waves from leaking from the outside. Magnetic sheets are Ni-based ferrite magnetic powder, Mg-based ferrite magnetic powder, Mn-based ferrite magnetic powder, Ba-based ferrite magnetic powder, Sr-based ferrite magnetic powder, Fe-Si alloy powder, Fe-Ni alloy powder. , Fe-Co alloy powder, Fe-Si-Al alloy powder, Fe-Si-Cr alloy powder, iron powder, Fe-based amorphous, Co-based amorphous, Fe-based nanocrystal, etc. Easy to demonstrate magnetic performance. An adhesive tape is used for this fixing. By fixing with the adhesive tape of the present invention, even if the magnetic sheet is thickened, it can be thinned as a composite (bonded product of magnetic sheet and adhesive tape).
以下に、この発明の実施例を記載して、より具体的に説明する。 Examples of the present invention will be described below in more detail.
(粘着剤の調製例1)
n−ブチルアクリレート:97.98部と、アクリル酸:2部と、4−ヒドロキシブチルアクリレート:0.02部とを、アゾビスイソブチロニトリル:0.2部を重合開始剤として、酢酸エチル溶液中で、80℃で8時間溶液重合を行って、重量平均分子量:90万のアクリル系ポリマーを得た。該アクリル系ポリマー:100部に、重合ロジンエステル(商品名「D−135」荒川化学社製):5部と、不均化ロジンエステル(商品名「KE−100」荒川化学社製):20部、石油樹脂(商品名「FTR6100」:25部)を加えて、酢酸エチルを加え、固形分40%の粘着剤溶液を調整した。さらにイソシアネート系架橋剤(商品名「NC40」DIC社製):0.8部を加えて、均一になるように撹拌して混合することにより、粘着剤Aを調製した。ゲル分率は20%であった。
(Adhesive Preparation Example 1)
n-butyl acrylate: 97.98 parts, acrylic acid: 2 parts, 4-hydroxybutyl acrylate: 0.02 part, azobisisobutyronitrile: 0.2 part as a polymerization initiator, ethyl acetate In the solution, solution polymerization was performed at 80 ° C. for 8 hours to obtain an acrylic polymer having a weight average molecular weight of 900,000. The acrylic polymer: 100 parts, polymerized rosin ester (trade name “D-135” manufactured by Arakawa Chemical Co., Ltd.): 5 parts, and disproportionated rosin ester (trade name “KE-100” manufactured by Arakawa Chemical Co., Ltd.): 20 Part, petroleum resin (trade name “FTR6100”: 25 parts) was added, and ethyl acetate was added to prepare an adhesive solution having a solid content of 40%. Further, an adhesive A was prepared by adding 0.8 parts of an isocyanate-based crosslinking agent (trade name “NC40” manufactured by DIC), and stirring and mixing so as to be uniform. The gel fraction was 20%.
(粘着剤の調製例2)
n−ブチルアクリレート:97.98部と、アクリル酸:2部と、4−ヒドロキシブチルアクリレート:0.02部とを、アゾビスイソブチロニトリル:0.3部を重合開始剤として、酢酸エチル溶液中で、90℃で6時間溶液重合を行って、重量平均分子量:50万のアクリル系ポリマーを得た。該アクリル系ポリマー:100部に、重合ロジンエステル(商品名「D−135」荒川化学社製):5部と、不均化ロジンエステル(商品名「KE−100」荒川化学社製):20部、石油樹脂(商品名「FTR6100」:25部)を加えて、酢酸エチルを加え、固形分40%の粘着剤溶液を調整した。さらにイソシアネート系架橋剤(商品名「NC40」DIC社製):1.5部を加えて、均一になるように撹拌して混合することにより、粘着剤Bを調製した。ゲル分率は30%であった。
(Adhesive Preparation Example 2)
n-butyl acrylate: 97.98 parts, acrylic acid: 2 parts, 4-hydroxybutyl acrylate: 0.02 part, azobisisobutyronitrile: 0.3 part as a polymerization initiator, ethyl acetate In the solution, solution polymerization was performed at 90 ° C. for 6 hours to obtain an acrylic polymer having a weight average molecular weight of 500,000. The acrylic polymer: 100 parts, polymerized rosin ester (trade name “D-135” manufactured by Arakawa Chemical Co., Ltd.): 5 parts, and disproportionated rosin ester (trade name “KE-100” manufactured by Arakawa Chemical Co., Ltd.): 20 Part, petroleum resin (trade name “FTR6100”: 25 parts) was added, and ethyl acetate was added to prepare an adhesive solution having a solid content of 40%. Furthermore, 1.5 parts of isocyanate-based crosslinking agent (trade name “NC40” manufactured by DIC) was added, and the mixture was stirred and mixed uniformly to prepare an adhesive B. The gel fraction was 30%.
(実施例1)
先ず、剥離フィルム(商品名「PET38×1K0」)に前記粘着剤Aを乾燥厚みが1.5μmとなるようロールコーターにて塗工し、100℃で1分乾燥し、これを支持体であるポリエステルフィルム(商品名「K100−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.26、熱収縮率:1.4%)に貼り合せる。この時の支持体の繰り出し張力は50N/mであり、剥離フィルムの貼り合せ張力は300N/mであった。次に、剥離フィルム(商品名)「PET25×1A3」に前記粘着剤Aを乾燥厚みが1.5μmとなるようロールコーターにて塗工し、100℃で1分乾燥し、前記支持体の粘着されていない面に貼り合せ、両面粘着テープ(厚み:5μm)を得た。
Example 1
First, the pressure-sensitive adhesive A is applied to a release film (trade name “PET38 × 1K0”) with a roll coater so that the dry thickness is 1.5 μm, and dried at 100 ° C. for 1 minute, and this is a support. A polyester film (trade name “K100-2.0W” manufactured by Mitsubishi Chemical Polyester Co., Ltd .; thickness: 2 μm, dynamic friction coefficient: 0.26, heat shrinkage ratio: 1.4%) is bonded. At this time, the feeding tension of the support was 50 N / m, and the bonding tension of the release film was 300 N / m. Next, the pressure-sensitive adhesive A was applied to a release film (trade name) “PET25 × 1A3” with a roll coater so that the dry thickness was 1.5 μm, and dried at 100 ° C. for 1 minute. A double-sided pressure-sensitive adhesive tape (thickness: 5 μm) was obtained by pasting on the surface that was not provided.
(実施例2)
粘着剤Aの乾燥厚みを1.5μの代わりに4μmにした以外は実施例1と同様にして、両面粘着テープ(厚み:10μm)を得た。
(Example 2)
A double-sided pressure-sensitive adhesive tape (thickness: 10 μm) was obtained in the same manner as in Example 1 except that the dry thickness of the pressure-sensitive adhesive A was changed to 4 μm instead of 1.5 μm.
(実施例3)
粘着剤Aの乾燥厚みを1.5μの代わりに0.5μmにした以外は実施例1と同様にして、両面粘着テープ(厚み:3μm)を得た。
(Example 3)
A double-sided pressure-sensitive adhesive tape (thickness: 3 μm) was obtained in the same manner as in Example 1 except that the dry thickness of the pressure-sensitive adhesive A was changed to 0.5 μm instead of 1.5 μm.
(実施例4)
支持体として、ポリエステルフィルム(商品名「K100−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.26、熱収縮率:1.4%)の代わりに、ポリエステルフィルム(商品名「K583−2.5W」三菱化学ポリエステル社製;厚さ:2.5μm、動摩擦係数:0.27、熱収縮率:1.5%)を用いた以外は実施例1と同様にして、両面粘着テープ(厚み:5.5μm)を得た。
Example 4
Instead of a polyester film (trade name “K100-2.0W” manufactured by Mitsubishi Chemical Polyester; thickness: 2 μm, dynamic friction coefficient: 0.26, thermal shrinkage: 1.4%) as a support, a polyester film ( The product name “K583-2.5W” manufactured by Mitsubishi Chemical Polyester; thickness: 2.5 μm, dynamic friction coefficient: 0.27, heat shrinkage ratio: 1.5%) was used in the same manner as in Example 1. A double-sided pressure-sensitive adhesive tape (thickness: 5.5 μm) was obtained.
(実施例5)
イソシアネート系架橋剤の添加量を0.8部の代わりに1.5部にした以外は実施例1と同様に両面粘着テープ(厚み:5.0μm)を得た。ゲル分率は30%であった。
(Example 5)
A double-sided pressure-sensitive adhesive tape (thickness: 5.0 μm) was obtained in the same manner as in Example 1 except that the amount of the isocyanate-based crosslinking agent added was 1.5 parts instead of 0.8 parts. The gel fraction was 30%.
(実施例6)
イソシアネート系架橋剤の添加量を0.8部の代わりに5.0部にした以外は実施例1と同様に両面粘着テープ(厚み:5.0μm)を得た。ゲル分率は50%であった。
(Example 6)
A double-sided pressure-sensitive adhesive tape (thickness: 5.0 μm) was obtained in the same manner as in Example 1 except that the amount of the isocyanate-based crosslinking agent added was 5.0 parts instead of 0.8 parts. The gel fraction was 50%.
(実施例7)
イソシアネート系架橋剤の添加量を0.8部の代わりに0.5部にした以外は実施例1と同様に両面粘着テープ(厚み:5.0μm)を得た。ゲル分率は5%であった。
(Example 7)
A double-sided pressure-sensitive adhesive tape (thickness: 5.0 μm) was obtained in the same manner as in Example 1 except that the addition amount of the isocyanate crosslinking agent was changed to 0.5 part instead of 0.8 part. The gel fraction was 5%.
(実施例8)
粘着剤Aの代わりに粘着剤Bを用いた以外は実施例1と同様に両面粘着テープ(厚み:5.0μm)を得た。ゲル分率は30%であった。
(Example 8)
A double-sided pressure-sensitive adhesive tape (thickness: 5.0 μm) was obtained in the same manner as in Example 1 except that the pressure-sensitive adhesive B was used instead of the pressure-sensitive adhesive A. The gel fraction was 30%.
(比較例1)
支持体として、ポリエステルフィルム(商品名「K100−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.26、熱収縮率:1.4%)の代わりに、ポリエステルフィルム(商品名「C660−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.30、熱収縮率:1.6%)を用いた以外は実施例1と同様にして、両面粘着テープ(厚み:5μm)を得た。
(Comparative Example 1)
Instead of a polyester film (trade name “K100-2.0W” manufactured by Mitsubishi Chemical Polyester; thickness: 2 μm, dynamic friction coefficient: 0.26, thermal shrinkage: 1.4%) as a support, a polyester film ( Product name “C660-2.0W” manufactured by Mitsubishi Chemical Polyester; thickness: 2 μm, dynamic friction coefficient: 0.30, heat shrinkage: 1.6%) An adhesive tape (thickness: 5 μm) was obtained.
(比較例2)
支持体として、ポリエステルフィルム(商品名「K100−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.26、熱収縮率:1.4%)の代わりに、ポリエステルフィルム(商品名「2DC61」東レ社製;厚さ:1.8μm、動摩擦係数:0.32、熱収縮率:1.5%)を用いた以外は実施例1と同様にして、両面粘着テープ(厚み:4.8μm)を得た。
(Comparative Example 2)
Instead of a polyester film (trade name “K100-2.0W” manufactured by Mitsubishi Chemical Polyester; thickness: 2 μm, dynamic friction coefficient: 0.26, thermal shrinkage: 1.4%) as a support, a polyester film ( Product name “2DC61” manufactured by Toray Industries, Inc .; thickness: 1.8 μm, dynamic friction coefficient: 0.32, heat shrinkage: 1.5%) : 4.8 μm).
(比較例3)
支持体として、ポリエステルフィルム(商品名「K100−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.26、熱収縮率:1.4%)の代わりに、ポリエステルフィルム(商品名「K917−1.5W」三菱化学ポリエステル社製;厚さ:1.5μm、動摩擦係数:0.27、熱収縮率:30%)を用いた以外は実施例1と同様にして、両面粘着テープ(厚み:4.5μm)を得た。
(Comparative Example 3)
Instead of a polyester film (trade name “K100-2.0W” manufactured by Mitsubishi Chemical Polyester; thickness: 2 μm, dynamic friction coefficient: 0.26, thermal shrinkage: 1.4%) as a support, a polyester film ( Product name “K917-1.5W” manufactured by Mitsubishi Chemical Polyester; thickness: 1.5 μm, dynamic friction coefficient: 0.27, heat shrinkage ratio: 30%) An adhesive tape (thickness: 4.5 μm) was obtained.
(比較例4)
支持体として、ポリエステルフィルム(商品名「K100−2.0W」三菱化学ポリエステル社製;厚さ:2μm、動摩擦係数:0.26、熱収縮率:1.4%)の代わりに、ポリエステルフィルム(商品名「S25」ユニチカ社製;厚さ:25μm、動摩擦係数:0.28、熱収縮率:1.0%)を用いた以外は実施例1と同様にして、両面粘着テープ(厚み:28μm)を得た。
(Comparative Example 4)
Instead of a polyester film (trade name “K100-2.0W” manufactured by Mitsubishi Chemical Polyester; thickness: 2 μm, dynamic friction coefficient: 0.26, thermal shrinkage: 1.4%) as a support, a polyester film ( Double-sided pressure-sensitive adhesive tape (thickness: 28 μm) in the same manner as in Example 1 except that the product name “S25” manufactured by Unitika Co., Ltd .; thickness: 25 μm, dynamic friction coefficient: 0.28, heat shrinkage rate: 1.0% was used. )
(支持体の動摩擦係数)
JISK7125に準じ、SUS鏡面とフィルム面の摩擦係数を測定した。図4のように裏打ち用片面粘着テープ「DIC製 PET50SER」21で裏打ちしたフィルム22を貼り、63mm×63mmのすべり片(重さ:1.96N)23と片面粘着テープ21が接するように固定した。次にそのすべり片に固定したフィルム22がSUS鏡面25と接するように置き、100mm/minですべり片23をロードセル26で引っ張り測定した。動摩擦係数は次式で算出した。
動摩擦係数[−]=動摩擦力[N]/1.96[N]
(Dynamic friction coefficient of support)
In accordance with JISK7125, the friction coefficient between the SUS mirror surface and the film surface was measured. As shown in FIG. 4, a
Coefficient of dynamic friction [−] = Dynamic friction force [N] /1.96 [N]
(支持体の収縮率)
JISC2151に従い測定した。100mm×100mのフィルムを150℃の乾燥器に30分放置し、乾燥器に入れる前後でのサイズをノギスで測定し、算出した。表には流れ(MD)・幅(TD)の最大値を記載した。
熱収縮率=100×(乾燥器に入れる前の長さー乾燥器に入れた後の長さ)/乾燥器に入れる前の長さ
(Shrinkage rate of support)
It measured according to JISC2151. A 100 mm × 100 m film was left in a drier at 150 ° C. for 30 minutes, and the size before and after placing in the drier was measured with a caliper and calculated. The table shows the maximum values of flow (MD) and width (TD).
Heat shrinkage rate = 100 × (length before being put in the dryer−length after being put in the dryer) / length before being put in the dryer
(ゲル分率)
実施例・比較例に使用した粘着剤をPET25μmフィルム(ユニチカ社製S25)に乾燥厚さ30μmとなるよう塗工する。養生後、トルエン中に浸漬し、24時間放置後に残った不溶分の乾燥後の質量を測定し、元の質量に対する百分率で表す。
ゲル分率=[(粘着剤層のトルエン浸漬後質量)/(粘着剤層のトルエン浸漬前質量)]×100
(Gel fraction)
The pressure-sensitive adhesive used in Examples and Comparative Examples is applied to a
Gel fraction = [(mass after pressure-sensitive adhesive layer is immersed in toluene) / (weight of pressure-sensitive adhesive layer before immersion in toluene)] × 100
(評価)
実施例、比較例に係る両面粘着テープについて、生産性、クリアランスの適合性、粘着力、高温保持力、耐熱収縮性をそれぞれ、下記の測定方法又は評価方法により測定又は評価した。評価結果は表1に示した。
(Evaluation)
About the double-sided adhesive tape which concerns on an Example and a comparative example, productivity, the suitability of clearance, adhesive force, high temperature holding power, and heat-resistant shrinkage were measured or evaluated by the following measuring method or evaluation method, respectively. The evaluation results are shown in Table 1.
(生産性)
ロール状に、シワなく良好な形態で両面粘着テープを作製することができるか否かで、判断し、作製できるものを「○」、作製できなかったものを「×」として評価した。評価結果は、表1の「生産性の可否」の欄に示した。
(productivity)
Judgment was made based on whether or not a double-sided pressure-sensitive adhesive tape could be produced in a roll and in a good form without wrinkles, and evaluation was made as “◯” for those that could be produced and “×” for those that could not be produced. The evaluation results are shown in the column of “productivity availability” in Table 1.
(クリアランスの適合性の評価方法)
両面粘着テープを、部品間のクリアランスが10μm以下となる部分に適用して、該クリアランスに適合させることができるか否かで判断し、適合できるものを「○」、適合できないものを「×」として評価した。評価結果は、表1の「クリアランスの適合性」の欄に示した。
(Evaluation method of clearance suitability)
Apply double-sided adhesive tape to the part where the clearance between parts is 10 μm or less, and judge whether it can be adapted to the clearance. As evaluated. The evaluation results are shown in the “clearance suitability” column of Table 1.
(粘着力の測定方法)
両面粘着テープを20mm幅に切断し、PET25μmで裏打ちした試験片を作製し、該試験片(20mm幅)について、JISZ−0237に準じて、テンシロン引張試験機を用いて、ピール粘着力(剥離角度:180°、引張速度:300mm/min、23℃×65%RH、被着体:ステンレス板)を測定した。測定結果は、表1の「粘着力(N/20mm)」の欄に示した。
(Measurement method of adhesive strength)
A double-sided adhesive tape was cut to a width of 20 mm, and a test piece backed with 25 μm of PET was prepared. The test piece (20 mm width) was peeled off using a Tensilon tensile tester according to JISZ-0237. : 180 °, tensile speed: 300 mm / min, 23 ° C. × 65% RH, adherend: stainless steel plate). The measurement results are shown in the column of “Adhesive strength (N / 20 mm)” in Table 1.
(高温保持力)
両面粘着テープを20mm幅に切断し、PET25μmで裏打ちした試験片を作製し、該試験片(20mm幅)について、JISZ−0237に準じて、鉛直方向に100g(20mm×20mm)の荷重をかけ、100℃雰囲気下で24時間放置し、24時間後のズレ距離を測定した。測定結果は、表1の「粘着力(N/20mm)」の欄に示した。
(High temperature holding power)
A double-sided pressure-sensitive adhesive tape was cut to a width of 20 mm, and a test piece backed with
(耐熱収縮性)
両面粘着テープを50mm×50mmに切断し、アルミ板に貼り合せ、100℃に72時間放置し、縮み距離を測定し、下記評価基準で評価した。
◎:0.1mm未満
○:0.1〜0.5mm
×:0.5mmを超える
(Heat-resistant shrinkage)
The double-sided adhesive tape was cut into 50 mm × 50 mm, bonded to an aluminum plate, left at 100 ° C. for 72 hours, the shrinkage distance was measured, and evaluated according to the following evaluation criteria.
A: Less than 0.1 mm O: 0.1-0.5 mm
×: Over 0.5 mm
表1より明らかなように、実施例1〜8の本発明の両面粘着テープは厚みが10μm以下と非常に薄膜であっても耐熱収縮性・生産性に優れていた。一方、比較例1,2のテープは生産時に支持体にシワが入りやすく、生産性に劣った。また比較例3の粘着テープは耐熱収縮性が著しく悪かった。比較例4のテープは厚く、スペースの無い部分で使用ができないものであった。 As is clear from Table 1, the double-sided pressure-sensitive adhesive tapes of the present invention of Examples 1 to 8 were excellent in heat shrinkage and productivity even if they were very thin films with a thickness of 10 μm or less. On the other hand, the tapes of Comparative Examples 1 and 2 were inferior in productivity because wrinkles were easily formed on the support during production. The pressure-sensitive adhesive tape of Comparative Example 3 was extremely poor in heat shrinkage. The tape of Comparative Example 4 was thick and could not be used where there was no space.
1 支持体
2,3 粘着剤層
4,5 剥離ライナー
11,17 剥離ライナー
12 粘着剤塗工装置
13 乾燥及び/又は紫外線照射装置
14 支持体
15 ラミネートロール
16 片面粘着テープ
18 両面粘着テープ
21 裏打ち用片面粘着テープ
22 フィルム(試験片)
23 すべり片
24 台座
25 SUS板
26 ロードセル(引張試験機)
DESCRIPTION OF SYMBOLS 1
23 Sliding
Claims (8)
工程(A1):剥離ライナーの剥離処理面に、粘着剤を塗布して前記剥離ライナー上に前記粘着剤層を形成する工程と、
工程(B1):前記支持体の一方の表面に、前記工程(A1)によって得られた剥離ライナー上に形成された前記粘着剤層を貼り合わせて、前記支持体上に第1の粘着剤層を形成する工程と、
工程(A2):前記剥離ライナーの他の剥離処理面に、粘着剤を塗布して前記剥離ライナー上に粘着剤を形成する工程と、
工程(B2): 前記工程(A2)を経て得られた粘着剤層付き剥離ライナーの粘着剤層と、前記工程(B1)を経て得られた支持体/粘着剤層/剥離ライナーが積層された片面粘着テープの支持体表面とを、ラミネートロールを通じて貼り合わせて、第2の粘着剤層を形成する工程、とを有する、ポリエステルフィルムからなる支持体の両面に、アクリル系粘着剤層を有する両面粘着テープの製造方法において、
総厚みが2〜10μmであり、前記支持体の厚みが1〜3μm、熱収縮率が3%以下、動摩擦係数が0.20〜0.28であって、放熱シートまたは磁性シートの固定に使用することを特徴とする両面粘着テープの製造方法。 A method for producing a double-sided pressure-sensitive adhesive tape having an acrylic pressure-sensitive adhesive layer on both sides of a support made of a polyester film,
Step (A1): Applying an adhesive to the release treatment surface of the release liner to form the adhesive layer on the release liner;
Step (B1): The pressure-sensitive adhesive layer formed on the release liner obtained in the step (A1) is bonded to one surface of the support, and the first pressure-sensitive adhesive layer is formed on the support. Forming a step;
Step (A2): a step of applying an adhesive to the other release treatment surface of the release liner to form an adhesive on the release liner;
Step (B2): The pressure-sensitive adhesive layer of the release liner with the pressure-sensitive adhesive layer obtained through the step (A2) and the support / pressure-sensitive adhesive layer / release liner obtained through the step (B1) were laminated. The both surfaces which have an acrylic adhesive layer on both surfaces of the support body which consists of a polyester film which have the process of bonding together the support body surface of a single-sided adhesive tape through a laminate roll, and forming a 2nd adhesive layer. In the method for producing an adhesive tape,
The total thickness is 2 to 10 μm, the thickness of the support is 1 to 3 μm, the heat shrinkage rate is 3% or less, the dynamic friction coefficient is 0.20 to 0.28, and it is used for fixing the heat dissipation sheet or the magnetic sheet. A method for producing a double-sided pressure-sensitive adhesive tape , comprising:
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JP2014105262A (en) * | 2012-11-27 | 2014-06-09 | Nippon Shokubai Co Ltd | Double-sided adhesive tape |
JP5887602B2 (en) * | 2013-03-28 | 2016-03-16 | 東洋インキScホールディングス株式会社 | Moisture curable hot melt adhesive |
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WO2015151223A1 (en) * | 2014-03-31 | 2015-10-08 | リンテック株式会社 | Double-sided adhesive sheet and double-sided adhesive sheet manufacturing method |
JP2016151006A (en) * | 2015-02-19 | 2016-08-22 | Dic株式会社 | Adhesive sheet, manufacturing method therefor and electronic device |
JP2016155950A (en) * | 2015-02-25 | 2016-09-01 | Dic株式会社 | Tacky-adhesive sheet, production method thereof, and electronic equipment |
JP6589359B2 (en) * | 2015-05-01 | 2019-10-16 | 三菱ケミカル株式会社 | Colored polyester film for adhesive tape substrate and adhesive tape |
JP6609983B2 (en) * | 2015-05-01 | 2019-11-27 | 三菱ケミカル株式会社 | Polyester film for adhesive tape substrate and adhesive tape |
JP6485213B2 (en) * | 2015-05-25 | 2019-03-20 | 三菱ケミカル株式会社 | Polyester film for adhesive tape substrate and adhesive tape |
JP2017014332A (en) * | 2015-06-29 | 2017-01-19 | Dic株式会社 | Adhesive tape and manufacturing method therefor, article and portable electronic terminal |
JP6365506B2 (en) * | 2015-10-31 | 2018-08-01 | 三菱ケミカル株式会社 | Laminated polyester film |
JP6428662B2 (en) * | 2016-01-27 | 2018-11-28 | 三菱ケミカル株式会社 | Laminated polyester film |
KR101828519B1 (en) * | 2016-04-08 | 2018-02-12 | 주식회사 영우 | Apparatus and method for manufacturing a heat-radiating film using a roll-to-roll process, and a method and apparatus for manufacturing a thermally conductive composite sheet using a roll-to-roll process including the heat- |
JP6859248B2 (en) * | 2017-10-26 | 2021-04-14 | 日本カーバイド工業株式会社 | Adhesive film and adhesive sheet |
JP6947605B2 (en) * | 2017-10-26 | 2021-10-13 | 日本カーバイド工業株式会社 | Adhesive film and adhesive sheet |
JP6747464B2 (en) * | 2018-03-02 | 2020-08-26 | 三菱ケミカル株式会社 | Laminated polyester film |
JP7463148B2 (en) * | 2019-03-18 | 2024-04-08 | 積水化学工業株式会社 | Adhesive Tape Roll |
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