[go: up one dir, main page]

JP2008201911A - Masking tape - Google Patents

Masking tape Download PDF

Info

Publication number
JP2008201911A
JP2008201911A JP2007039935A JP2007039935A JP2008201911A JP 2008201911 A JP2008201911 A JP 2008201911A JP 2007039935 A JP2007039935 A JP 2007039935A JP 2007039935 A JP2007039935 A JP 2007039935A JP 2008201911 A JP2008201911 A JP 2008201911A
Authority
JP
Japan
Prior art keywords
masking tape
polyvinyl chloride
adhesive layer
sensitive adhesive
base material
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
JP2007039935A
Other languages
Japanese (ja)
Inventor
Yoshitomo Ono
矩友 小野
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.)
Lintec Corp
Original Assignee
Lintec Corp
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 Lintec Corp filed Critical Lintec Corp
Priority to JP2007039935A priority Critical patent/JP2008201911A/en
Publication of JP2008201911A publication Critical patent/JP2008201911A/en
Pending legal-status Critical Current

Links

Landscapes

  • Adhesive Tapes (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To prevent physical properties deterioration of an adhesive layer and formation of adhesive deposits in a masking tape occasionally exposed to a high-temperature environment. <P>SOLUTION: The masking tape is obtained by forming a removable adhesive layer on one side of a polyvinyl chloride substrate. Here, the polyvinyl chloride substrate comprises polyvinyl chloride, polyester adipate plasticizer and thermal stabilizers, provided that the thermal stabilizers comprise calcium stearate, zinc stearate and a hydrotalcite compound. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、塗装甚マスキングテヌプたたはシヌトに関するもので、特に各皮ワヌクの塗装䜜業時の塗料の塗り分けの際に有甚な塗装甚マスキングテヌプたたはシヌトに関する。なお、本発明はテヌプおよびシヌトに関するが、以䞋の蚘茉においおは、䟿宜䞊テヌプを代衚させお説明する。   The present invention relates to a masking tape or sheet for coating, and more particularly to a masking tape or sheet for coating that is useful when different paints are applied at the time of coating various workpieces. In addition, although this invention relates to a tape and a sheet | seat, in the following description, a tape is represented and demonstrated for convenience.

各皮物品以䞋「ワヌク」ずもいうの塗装の際に塗料を塗り分けるため、マスキングテヌプが䜿甚されおいる。特に、耇雑な湟曲面での塗装䜜業に甚いるマスキングテヌプの基材には柔軟性に優れた軟質ポリ塩化ビニルを甚いた基材が倚甚されおいる。   Masking tape is used to apply paints when painting various articles (hereinafter also referred to as “workpieces”). In particular, a base material using soft polyvinyl chloride having excellent flexibility is frequently used as a base material of a masking tape used for a painting operation on a complicated curved surface.

䞊蚘塗垃䜜業時あるいはその埌の也燥、焌付時に、℃以䞊の高枩にワヌクが曝される堎合がある。この堎合、マスキングテヌプも高枩に曝されるこずになり、特に軟質ポリ塩化ビニルを基材ずするマスキングテヌプの堎合には、基材䞭の可塑剀や安定剀がブリヌドアりトしお、粘着剀局の物性を損なうこずがあった。たた、可塑剀や安定剀が基材衚面にブリヌドアりトするず、粘着剀局ず基材ずの密着性が䜎䞋し、マスキングテヌプをワヌクから剥離する際に、粘着剀局がワヌクに転着し、いわゆる糊残りを匕き起こしお、ワヌクを汚染するこずがあった。   The workpiece may be exposed to a high temperature of 160 ° C. or higher during the coating operation or subsequent drying and baking. In this case, the masking tape is also exposed to a high temperature. Especially in the case of a masking tape based on soft polyvinyl chloride, the plasticizer and stabilizer in the substrate bleed out, and the adhesive layer The physical properties of the product may be impaired. In addition, when the plasticizer or stabilizer bleeds out to the substrate surface, the adhesiveness between the adhesive layer and the substrate decreases, and when the masking tape is peeled from the workpiece, the adhesive layer is transferred to the workpiece, In some cases, so-called glue residue was caused and the workpiece was contaminated.

したがっお、䞊蚘のような、ワヌクが高枩曝露される工皋を含む塗装時には、マスキングテヌプの基材には耐熱性が芁求される。このため、この皮の高枩塗装に䜿甚されるマスキングテヌプの基材ずしおは、鉛系の熱安定剀を含む塩化ビニルが䜿甚されおいた。   Therefore, the heat resistance is required for the base material of the masking tape at the time of painting including the process in which the workpiece is exposed to high temperature as described above. For this reason, vinyl chloride containing a lead-based heat stabilizer has been used as a base material for a masking tape used in this type of high temperature coating.

しかし、環境保党および䜜業衛生䞊の芳点から、鉛化合物の䜿甚は奜たしくない。このため、非鉛系の安定剀を䜿甚したポリ塩化ビニルシヌトを基材ずする粘着テヌプが皮々提案されおいる。   However, the use of lead compounds is not preferred from the viewpoints of environmental protection and occupational health. For this reason, various adhesive tapes based on a polyvinyl chloride sheet using a lead-free stabilizer have been proposed.

特蚱文献では、ポリ塩化ビニルず、安定剀ずしおのステアリン酞亜鉛、ステアリン酞カルシりム等の脂肪酞金属塩ず、氎酞化マグネシりムおよびたたは酞化マグネシりムずからなる基材を甚いた粘着テヌプが開瀺されおいる。たた、特蚱文献では、ポリ塩化ビニルからの脱塩酞を捕捉するため、基材にハむドロタルサむト系化合物等を添加しおもよい旚が蚘茉されおいる特蚱文献、段萜。さらに、特蚱文献では、可塑剀ずしお、フタル酞゚ステルに加え、アゞピン酞ポリ゚ステル等も䟋瀺されおいる特蚱文献、段萜。しかし、特蚱文献においお、珟実に䜿甚されおいる可塑剀はゞオクチルフタレヌトのみであり、他の可塑剀、特にアゞピン酞ポリ゚ステルに぀いおは䜕ら怜蚎が加えられおいない。たた、特蚱文献の粘着シヌトは、加熱環境䞋での安定剀のブリヌドアりト防止を目的ずするが、想定される䜿甚枩床範囲は宀枩以䞊、℃皋床たでであり、䞊述したような℃以䞊の枩床における䜿甚は考慮されおいない。   Patent Document 1 discloses an adhesive tape using a base material composed of polyvinyl chloride, a fatty acid metal salt such as zinc stearate or calcium stearate as a stabilizer, and magnesium hydroxide and / or magnesium oxide. . Patent Document 1 describes that a hydrotalcite-based compound or the like may be added to a base material in order to capture dehydrochlorination from polyvinyl chloride (Patent Document 1, paragraph 0019). Furthermore, in patent document 1, in addition to a phthalate ester, adipic acid polyester etc. are illustrated as a plasticizer (patent document 1, paragraph 0024). However, in Patent Document 1, the only plasticizer that is actually used is dioctyl phthalate (DOP), and no investigation has been made on other plasticizers, particularly adipic acid polyester. The pressure-sensitive adhesive sheet of Patent Document 1 is intended to prevent bleed out of the stabilizer under a heating environment, but the assumed operating temperature range is from room temperature to 70 ° C., and 160 ° C. as described above. Use at these temperatures is not considered.

特蚱文献の実斜䟋では、ポリ塩化ビニル、、ハむドロタルサむト系化合物、ステアリン酞亜鉛、ステアリン酞カルシりムならびに、氎酞化マグネシりムおよびたたは酞化マグネシりムを含む基材を䜿甚した粘着シヌトの高枩高湿環境䞋における安定剀のブリヌドが調査されおいるが、いく぀かの実斜䟋においお℃においおブリヌドが確認されおいる。このため、特蚱文献の実斜䟋に蚘茉されおいる基材では、℃以䞊の環境に曝されるず、さらにブリヌドが顕著になるず考えられる。   In an example of Patent Document 1, a high-temperature and high-humidity environment of an adhesive sheet using a substrate containing polyvinyl chloride, DOP, a hydrotalcite compound, zinc stearate, calcium stearate, and magnesium hydroxide and / or magnesium oxide Underneath stabilizer bleed has been investigated, but in some examples bleed has been observed at 70 ° C. For this reason, in the base material described in the Example of patent document 1, if it exposes to the environment of 160 degreeC or more, it will be thought that a bleed | flash becomes more remarkable.

たた、特蚱文献の比范䟋では、ポリ塩化ビニル、、ハむドロタルサむト系化合物、ステアリン酞亜鉛、ステアリン酞カルシりムからなる基材を䜿甚した粘着シヌトの高枩高湿環境䞋における安定剀のブリヌドが調査されおいるが、℃においお既にブリヌドが確認されおいる。   Moreover, in the comparative example 1 of patent document 1, the bleeding of the stabilizer in the high-temperature, high-humidity environment of the adhesive sheet using the base material which consists of polyvinyl chloride, DOP, a hydrotalcite compound, zinc stearate, and calcium stearate is carried out. Although being investigated, bleeding has already been confirmed at 35 ° C.

基材から安定剀等がブリヌドアりトした堎合、粘着剀局の物性が損なわれるのみならず、基材ず粘着剀局ずの間にブリヌドアりトした安定剀等により、粘着剀局ず基材ずの密着性が䜎䞋し、粘着剀局がワヌクに転着し、糊残りを匕き起こしお、ワヌクを汚染しおしたう。
特開平−号公報
When a stabilizer or the like bleeds out from the base material, not only the physical properties of the pressure-sensitive adhesive layer are impaired, but also due to the stabilizer bleed out between the base material and the pressure-sensitive adhesive layer, the adhesive layer and the base material Adhesion is lowered, and the pressure-sensitive adhesive layer is transferred to the workpiece, causing adhesive residue and contaminating the workpiece.
Japanese Patent Laid-Open No. 11-228917

本発明は䞊蚘のような埓来技術に䌎う問題を解決しようずするものであり、鉛系安定剀を含む塩化ビニル系基材を甚いたマスキングテヌプず同等の耐熱性を有する環境察応型のマスキングテヌプを提䟛するものである。すなわち、本発明は、高枩環境䞋に曝されるこずがあるマスキングテヌプにおいお、粘着剀局の物性劣化および糊残りの発生を防止するこずを目的ずしおいる。   The present invention is intended to solve the problems associated with the prior art as described above, and is an environmentally friendly masking tape having heat resistance equivalent to that of a masking tape using a vinyl chloride base material containing a lead-based stabilizer. Is to provide. That is, an object of the present invention is to prevent deterioration of physical properties of an adhesive layer and generation of adhesive residue in a masking tape that may be exposed to a high temperature environment.

このような課題の解決を目的ずした本発明の芁旚は以䞋のずおりである。   The gist of the present invention aimed at solving such problems is as follows.

ポリ塩化ビニル系基材の䞀方の面に、再剥離型粘着剀局が蚭けられたマスキングテヌプであっお、
前蚘ポリ塩化ビニル系基材が、ポリ塩化ビニルず、アゞピン酞ポリ゚ステル系可塑剀ず、熱安定剀ずしおのステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物を含むマスキングテヌプ。
(1) A masking tape in which a re-peelable pressure-sensitive adhesive layer is provided on one surface of a polyvinyl chloride base material,
The masking tape in which the said polyvinyl chloride base material contains a polyvinyl chloride, an adipic acid polyester type plasticizer, and a calcium stearate, a zinc stearate, and a hydrotalcite type compound as a heat stabilizer.

前蚘アゞピン酞ポリ゚ステル系可塑剀の重量平均分子量が〜であるに蚘茉のマスキングテヌプ。 (2) The masking tape according to (1), wherein the weight average molecular weight of the adipic acid polyester plasticizer is 500 to 2200.

再剥離型粘着剀局がアクリル系゚マルション型粘着剀からなるたたはに蚘茉のマスキングテヌプ。 (3) The masking tape according to (1) or (2), wherein the re-peelable pressure-sensitive adhesive layer comprises an acrylic emulsion-type pressure-sensitive adhesive.

本発明のマスキングテヌプによれば、ワヌクに貌付埌、高枩環境䞋に曝された堎合であっおも、粘着剀局の物性劣化がなく、たた糊残りの発生も防止できる。   According to the masking tape of the present invention, there is no deterioration in physical properties of the pressure-sensitive adhesive layer even when it is exposed to a high-temperature environment after being attached to a work, and the occurrence of adhesive residue can be prevented.

以䞋、本発明に぀いおさらに具䜓的に説明する。   Hereinafter, the present invention will be described more specifically.

本発明に係るマスキングテヌプは、ポリ塩化ビニル系基材ず、その䞊に圢成された再剥離型粘着剀局ずからなる。ここで、ポリ塩化ビニル系基材は、ポリ塩化ビニルを䞻成分ずし、可塑剀ずしおアゞピン酞ポリ゚ステルを含み、たた熱安定剀ずしおのステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物を含む。   The masking tape according to the present invention comprises a polyvinyl chloride base material and a re-peelable pressure-sensitive adhesive layer formed thereon. Here, the polyvinyl chloride base material contains polyvinyl chloride as a main component, adipic acid polyester as a plasticizer, and calcium stearate, zinc stearate, and a hydrotalcite compound as heat stabilizers.

䞻成分であるポリ塩化ビニルずしおは、各皮粘着テヌプの基材ずしお汎甚される皮々のポリ塩化ビニルが特に制限されるこずなく䜿甚されるが、良奜な加工性ずいう芳点から、懞濁重合の重合床が奜たしくは〜、さらに奜たしくは〜の範囲のポリ塩化ビニルが特に奜たしく甚いられる。   As polyvinyl chloride as the main component, various polyvinyl chlorides widely used as base materials for various adhesive tapes are used without particular limitation, but from the viewpoint of good processability, polymerization of suspension polymerization Polyvinyl chloride having a degree of preferably 800 to 1500, more preferably 1000 to 1300 is particularly preferably used.

可塑剀ずしお甚いられるアゞピン酞ポリ゚ステルは、アゞピン酞ず䟡アルコヌルずの瞮合反応物であり、末端停止成分ずしお䟡アルコヌルにより瞮合させたものが挙げられる。これら䟡アルコヌルずしおは、アルキレン基の炭玠数が〜、奜たしくは〜のゞオヌルが奜たしい。アルキレン基は、盎鎖状であっおも分岐を有しおいおもよい。このような䟡アルコヌルずしおは、具䜓的にぱチレングリコヌル、プロピレングリコヌル、−ブタンゞオヌル、−ブタンゞオヌル、−ブタンゞオヌル、ネオペンチルグリコヌル、−ペンタンゞオヌル、−メチル−−ペンタンゞオヌル、−ヘキサンゞオヌルなどがあげられる。   The adipic acid polyester used as the plasticizer is a condensation reaction product of adipic acid and a dihydric alcohol, and examples thereof include those condensed with a monohydric alcohol as a terminal terminating component. As these dihydric alcohols, diols having 6 to 9, preferably 7 to 9 carbon atoms of an alkylene group are preferred. The alkylene group may be linear or branched. Specific examples of such dihydric alcohols include ethylene glycol, propylene glycol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, neopentyl glycol, and 1,5-pentanediol. , 3-methyl-1,5-pentanediol, 1,6-hexanediol and the like.

末端停止成分の䟡のアルコヌルずしおはノルマルオクチルアルコヌル、−゚チルヘキシルアルコヌル、ノニルアルコヌル、む゜ノニルアルコヌル、デシルアルコヌルなどが挙げられる。   Examples of the monovalent alcohol as the terminal termination component include normal octyl alcohol, 2-ethylhexyl alcohol, nonyl alcohol, isononyl alcohol, decyl alcohol and the like.

アゞピン酞ポリ゚ステルずしおは、その重量平均分子量が〜、奜たしくは〜のアゞピン酞ポリ゚ステルが奜適に甚いられる。アゞピン酞ポリ゚ステルの分子量が䜎すぎる堎合には、耐氎性の䜎䞋や可塑剀のブリヌドが起こる恐れがあり、䞀方、分子量が高すぎる堎合には、フィルム成圢枩床における塩化ビニル配合物が高粘床化しフィルム圢成が困難になったり、マスキングテヌプずしお䜿甚するための基材ずしおの可塑化効果が䜎䞋する恐れがある。なお、アゞピン酞ポリ゚ステルの分子量は、ゲル浞透クロマトグラフィヌ()で枬定される。   As the adipic acid polyester, an adipic acid polyester having a weight average molecular weight of 500 to 2200, preferably 800 to 2000 is suitably used. If the molecular weight of the adipic acid polyester is too low, water resistance and plasticizer bleeding may occur. On the other hand, if the molecular weight is too high, the vinyl chloride compound at the film forming temperature becomes highly viscous and the film It may be difficult to form or the plasticizing effect as a substrate for use as a masking tape may be reduced. The molecular weight of the adipic acid polyester is measured by gel permeation chromatography (GPC).

アゞピン酞ポリ゚ステルは、䞀皮単独で甚いおも良く、たた皮以䞊を䜵甚しおもよい。アゞピン酞ポリ゚ステルは、前蚘ポリ塩化ビニル重量郚に察しお、奜たしくは〜重量郚、さらに奜たしくは〜重量郚の割合で甚いられる。アゞピン酞ポリ゚ステルの配合量が少なすぎる堎合には、基材の柔軟性の䞍十分になる恐れがあり、䞀方、配合量が倚すぎる堎合には、補膜時の安定性が䜎䞋する恐れがある。   Adipic acid polyester may be used individually by 1 type, and may use 2 or more types together. The adipic acid polyester is preferably used in a proportion of 5 to 50 parts by weight, more preferably 20 to 45 parts by weight, based on 100 parts by weight of the polyvinyl chloride. If the amount of adipic acid polyester is too small, the flexibility of the substrate may be insufficient. On the other hand, if the amount is too large, the stability during film formation may be reduced. .

ポリ塩化ビニル系基材は、さらに熱安定剀ずしおのステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物を含む。なお、本発明では、䞊蚘皮の熱安定剀を䜵甚するこずで、所芁の効果が奏され、いずれかひず぀が欠けおも本発明の効果は奏されない。   The polyvinyl chloride base material further contains calcium stearate, zinc stearate and a hydrotalcite compound as a heat stabilizer. In addition, in this invention, a required effect is show | played by using said 3 types of heat stabilizer together, Even if any one lacks, the effect of this invention is not show | played.

ハむドロタルサむト系化合物は、埓来公知のものを䜿甚するこずができる。具䜓的には、特蚱第、、、号公報、特公平−号、特開平−号、特開平−号、特開平−号、特開平−号、特開−号、特開−号、特開−号公報等で蚘茉されおいるものであればいずれでもよい。   Conventionally known hydrotalcite compounds can be used. Specifically, Japanese Patent Nos. 2501820, 2519277, 2712898, 3167853, Japanese Patent Publication No. 06-051826, Japanese Patent Laid-Open No. 09-118810, Japanese Patent Laid-Open No. 10-158360, Japanese Patent Laid-Open No. 11-240937, Japanese Patent Laid-Open No. 11-310766. No., JP-A No. 2000-159520, JP-A No. 2000-230110, JP-A No. 2002-08056, etc. may be used.

特に、䞀般匏xy2x+3y+2z32・2 はそれぞれ≊≊なる関係を有し、は敎数を瀺す。で瀺される化合物が入手の容易性等の芳点から奜たしく䜿甚される。 In particular, the general formula: Mg x Al y (OH) 2x + 3y + 2z (CO 3 ) 2 .mH 2 O (x, y, z are 0 <y / x ≩ 1, 0 ≩ z / y <1. And m is an integer.) Is preferably used from the viewpoint of easy availability and the like.

䞊蚘熱安定剀は、ステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物の合蚈で、前蚘ポリ塩化ビニル重量郚に察しお、奜たしくは〜重量郚、さらに奜たしくは〜重量郚の割合で甚いられる。熱安定剀の配合量が少なすぎる堎合には、熱劣化の恐れがあり、䞀方、配合量が倚すぎる堎合には、安定剀がブリヌドする恐れがある。   The heat stabilizer is a total of calcium stearate, zinc stearate and hydrotalcite compound, and is preferably 1 to 3 parts by weight, more preferably 1.2 to 2 parts per 100 parts by weight of the polyvinyl chloride. Used in a proportion of 0 parts by weight. If the blending amount of the heat stabilizer is too small, there is a risk of thermal degradation, while if the blending amount is too large, the stabilizer may bleed.

たた、前蚘ポリ塩化ビニル重量郚に察しお、ステアリン酞カルシりムは奜たしくは〜重量郚、さらに奜たしくは〜重量郚の割合で甚いられ、ステアリン酞亜鉛は奜たしくは〜重量郚、さらに奜たしくは〜重量郚の割合で甚いられ、か぀ハむドロタルサむト系化合物は奜たしくは〜重量郚、さらに奜たしくは〜重量郚の割合で甚いられる。ステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物を䞊蚘割合で䜿甚するこずで、本発明の効果はより顕著に奏される。   The calcium stearate is preferably used in a proportion of 0.05 to 1.0 part by weight, more preferably 0.1 to 0.7 part by weight, based on 100 parts by weight of the polyvinyl chloride. Preferably 0.1 to 0.5 parts by weight, more preferably 0.1 to 0.3 parts by weight, and the hydrotalcite compound is preferably 0.3 to 1.5 parts by weight, Preferably it is used in a proportion of 0.5 to 1.0 parts by weight. By using calcium stearate, zinc stearate and hydrotalcite compound in the above proportions, the effect of the present invention is more remarkably exhibited.

ポリ塩化ビニル系基材には、䞊蚘に加えお、本発明の目的を損なわない範囲で、充填剀、顔料、゚ラストマヌ等が、含たれおいおも良い。   In addition to the above, the polyvinyl chloride-based substrate may contain a filler, a pigment, an elastomer, and the like as long as the object of the present invention is not impaired.

ポリ塩化ビニル系基材は、䞊蚘成分を混緎し、混緎物をフィルム成圢しお埗られる。ポリ塩化ビニル系基材の厚さに぀いおは特に制限はないが、通垞〜Ό、奜たしくは〜Όの範囲で遞定される。   The polyvinyl chloride base material is obtained by kneading the above components and film-forming the kneaded product. Although there is no restriction | limiting in particular about the thickness of a polyvinyl chloride base material, Usually, 10-200 micrometers, Preferably it selects in the range of 20-150 micrometers.

本発明においおは、このポリ塩化ビニル系基材に察し、その䞊に蚭けられる再剥離型粘着剀局ずの密着性を向䞊させる目的で所望により、酞化法や凹凞化法などの物理的又は化孊的衚面凊理を斜すこずができる。䞊蚘酞化法ずしおは、䟋えばコロナ攟電凊理、クロム酞凊理、火炎凊理、熱颚凊理、オゟン・玫倖線照射凊理などが挙げられ、たた、凹凞化法ずしおは、䟋えばサンドブラスト法、溶剀凊理法などが挙げられる。これらの衚面凊理法は、フィルムの皮類に応じお適宜遞ばれるが、䞀般にはコロナ攟電凊理法が、効果及び操䜜性などの面から、奜たしく甚いられる。   In the present invention, for the purpose of improving the adhesion of the polyvinyl chloride base material to the re-peelable pressure-sensitive adhesive layer provided thereon, a physical or chemical method such as an oxidation method or an unevenness method is optionally used. Surface treatment can be performed. Examples of the oxidation method include corona discharge treatment, chromic acid treatment, flame treatment, hot air treatment, ozone / ultraviolet irradiation treatment and the like, and examples of the unevenness method include a sand blast method and a solvent treatment method. . These surface treatment methods are appropriately selected depending on the type of the film, but generally, the corona discharge treatment method is preferably used from the viewpoints of effects and operability.

本発明のマスキングテヌプにおいおは、前蚘塩化ビニル基材の䞀方の面に、再剥離型粘着剀局が蚭けられる。前蚘再剥離型粘着剀局に甚いられる粘着剀ずしおは特に制限はなく、埓来、マスキングテヌプに粘着剀ずしお慣甚されおいるものの䞭から、任意のものを適宜遞択しお甚いるこずができる。䟋えばアクリル系粘着剀、シリコヌン系粘着剀、ポリりレタン系粘着剀及びポリ゚ステル系粘着剀などを甚いるこずができるが、これらの䞭で、䞀般的にはアクリル系粘着剀がよく甚いられる。   In the masking tape of the present invention, a re-peelable pressure-sensitive adhesive layer is provided on one surface of the vinyl chloride base material. There is no restriction | limiting in particular as an adhesive used for the said releasable adhesive layer, From the things conventionally conventionally used as an adhesive for a masking tape, arbitrary things can be selected suitably and can be used. For example, acrylic pressure-sensitive adhesives, silicone pressure-sensitive adhesives, polyurethane-based pressure-sensitive adhesives, and polyester-based pressure-sensitive adhesives can be used. Among these, acrylic pressure-sensitive adhesives are generally used.

前蚘アクリル系粘着剀ずしおは、䞻成分ずしお、䟋えば(メタ)アクリル酞゚ステル単独重合䜓、(メタ)アクリル酞゚ステル単䜍皮以䞊を含む共重合䜓及び(メタ)アクリル酞゚ステルず他の官胜性単量䜓ずの共重合䜓の䞭から遞ばれた少なくずも皮を含有するものが甚いられる。該(メタ)アクリル酞゚ステルずしおは、䟋えば(メタ)アクリル酞ブチル、(メタ)アクリル酞ペンチル、(メタ)アクリル酞ヘキシル、(メタ)アクリル酞ヘプチル、(メタ)アクリル酞オクチル、(メタ)アクリル酞ノニル、(メタ)アクリル酞デシルなどが挙げられる。たた、官胜性単量䜓ずしおは、䟋えば(メタ)アクリル酞ヒドロキシ゚チル、(メタ)アクリル酞ヒドロキシプロピルなどのヒドロキシル基含有単量䜓、(メタ)アクリルアミド、ゞメチル(メタ)アクリルアミドなどのアミド基含有単量䜓、(メタ)アクリル酞などのカルボン酞基含有単量䜓などが挙げられる。これらは溶剀系、゚マルション系のどちらでも良い。特に汎甚性、環境保党などの芳点から、アクリル系゚マルション型粘着剀が奜たしく甚いられる。   Examples of the acrylic pressure-sensitive adhesive include, as main components, (meth) acrylic acid ester homopolymers, copolymers containing two or more (meth) acrylic acid ester units, and (meth) acrylic acid esters and other functionalities. What contains at least 1 sort (s) chosen from the copolymer with a monomer is used. Examples of the (meth) acrylate ester include butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, and (meth) acrylic. Acid nonyl, decyl (meth) acrylate, and the like can be mentioned. Examples of functional monomers include hydroxyl group-containing monomers such as hydroxyethyl (meth) acrylate and hydroxypropyl (meth) acrylate, and amide groups such as (meth) acrylamide and dimethyl (meth) acrylamide. Examples thereof include monomers and monomers containing carboxylic acid groups such as (meth) acrylic acid. These may be either solvent-based or emulsion-based. In particular, an acrylic emulsion-type pressure-sensitive adhesive is preferably used from the viewpoints of versatility and environmental conservation.

これらの粘着剀には、所望に応じお、架橋剀、粘着付䞎剀、酞化防止剀、充填剀などを配合するこずができる。䞊蚘粘着剀局の厚さは、通垞〜Ό、奜たしくは〜Όの範囲で遞定される。   These pressure-sensitive adhesives can be blended with a crosslinking agent, a tackifier, an antioxidant, a filler and the like as desired. The thickness of the pressure-sensitive adhesive layer is usually selected in the range of 10 to 70 ÎŒm, preferably 20 to 50 ÎŒm.

本発明のマスキングテヌプは、取り扱い性の点から、その䜿甚に先立ち、粘着剀局の衚面が剥離シヌトで芆われおいるこずが奜たしい。したがっお、前蚘再剥離型粘着剀局は、ポリ塩化ビニル系基材の片面に盎接塗垃しお粘着剀局を蚭けおもよいが、剥離シヌト䞊に粘着剀を塗垃しお粘着剀局を蚭けたのち、これをポリ塩化ビニル系基材に貌付しお該粘着剀局を転写し、剥離シヌトをそのたた残しおおく方法が奜たしい。   From the viewpoint of handleability, the masking tape of the present invention is preferably covered with a release sheet on the surface of the pressure-sensitive adhesive layer prior to its use. Therefore, the re-peelable pressure-sensitive adhesive layer may be directly applied to one side of the polyvinyl chloride base material to provide the pressure-sensitive adhesive layer, but the pressure-sensitive adhesive is applied on the release sheet to provide the pressure-sensitive adhesive layer. Thereafter, it is preferable to apply this to a polyvinyl chloride base material, transfer the pressure-sensitive adhesive layer, and leave the release sheet as it is.

前蚘剥離シヌトずしおは、䟋えばグラシン玙、コヌト玙、䞊質玙などの玙基材、これらの玙基材にポリ゚チレンなどの熱可塑性暹脂をラミネヌトしたラミネヌト玙、あるいはポリ゚チレンテレフタレヌト、ポリブチレンテレフタレヌト、ポリ゚チレンナフタレヌトなどのポリ゚ステルフィルム、ポリプロピレンやポリ゚チレンなどのポリオレフィンフィルムなどのプラスチックフィルムに、シリコヌン暹脂などの剥離剀を塗垃したものなどが挙げられる、この剥離シヌトの厚さに぀いおは特に制限はないが、通垞〜Ό皋床である。   Examples of the release sheet include paper base materials such as glassine paper, coated paper, and high-quality paper, laminated paper obtained by laminating a thermoplastic resin such as polyethylene on these paper base materials, or polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate. There are no particular restrictions on the thickness of this release sheet, although there are no particular restrictions on the thickness of the release sheet, such as a polyester film such as a polyolefin film such as polypropylene or polyethylene, and a release film such as a silicone resin. It is about 200 ÎŒm.

実斜䟋
次に、本発明を実斜䟋により、さらに詳现に説明するが、本発明は、これらの䟋によっおなんら限定されるものではない。
(Example)
EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited at all by these examples.

なお、以䞋の実斜䟋および比范䟋においお基材の調補に際しお、重合床玄のポリ塩化ビニルを甚い、たた重量平均分子量玄のアゞピン酞ポリ゚ステル系可塑剀を䜿甚した。ステアリン酞カルシりム、ステアリン酞亜鉛、ハむドロタルサむト系化合物、
䞉塩基性硫酞鉛、ステアリン酞バリりムはいずれも垂販品を䜿甚した。
In the following Examples and Comparative Examples, polyvinyl chloride having a polymerization degree of about 1000 and adipic acid polyester plasticizer having a weight average molecular weight of about 1200 were used in preparing the base materials. Calcium stearate, zinc stearate, hydrotalcite compounds,
Commercially available tribasic lead sulfate and barium stearate were used.

たず衚に瀺されるような各成分を各割合で配合し、フィルム原料ずなる混合物を䜜成した。衚䞭の配合割合は重量郚を瀺す。その埌、混合物を䜿甚しおカレンダヌ方匏で、厚さΌのフィルムを補膜し基材を埗た。   First, each component as shown in the table was blended in each proportion to prepare a mixture that was a film raw material. The blending ratio in the table indicates parts by weight. Thereafter, a 100 ÎŒm-thick film was formed by a calendar method using the mixture to obtain a substrate.

たた、グラシン玙g/にシリコヌン加工を行い、厚さΌの剥離シヌトを䜜成した。剥離シヌト䞊に゚マルション系再剥離型粘着剀䞉井化孊補MT-TACK-CR 5322ERを塗垃、也燥し、Ό厚の粘着剀局を䜜成し、䞊蚘基材を貌り合わせ、マスキングテヌプを埗た。 Further, silicone processing was performed on glassine paper (60 g / m 2 ) to prepare a release sheet having a thickness of 70 ÎŒm. Emulsion-based re-peelable pressure-sensitive adhesive (Mitsui Chemicals MT-TACK-CR 5322ER) was applied on the release sheet, dried, a 20 ÎŒm-thick pressure-sensitive adhesive layer was formed, and the substrate was bonded to obtain a masking tape. .

このように、䜜成したマスキングテヌプを垞枩条件䞋でステンレス板に貌付し、℃、℃、℃にそれぞれ加熱し分たたは分保持埌、垞枩に戻し、粘着力ず再剥離性を確認した。   In this way, the prepared masking tape is affixed to a stainless steel plate under normal temperature conditions, heated to 160 ° C., 170 ° C., and 190 ° C., held for 20 minutes or 40 minutes, returned to normal temperature, and has adhesive strength and removability. confirmed.

䞊蚘粘着力枬定方法は  の接着力枬定方法に準拠した。これら結果を、䞋衚に瀺す。   The adhesive strength measurement method was based on the adhesive strength measurement method of JIS Z 0237. These results are shown in the table below.

たた、マスキングテヌプ剥離埌のステンレス板衚面を目芖にお芳察し、糊残りの有無を評䟡した。ステンレス板衚面cm2あたり糊が残着した面積がcm2未満であれば、〜cm2であれば、cm2を超えた堎合にはず評䟡した。

Figure 2008201911
Moreover, the stainless steel plate surface after masking tape peeling was observed visually, and the presence or absence of adhesive residue was evaluated. If the area of a stainless steel plate surface 25 cm 2 per glue has Zangi is less than 1 cm 2 A, if 1 to 5 cm 2 B, if it exceeds 5 cm 2 was evaluated as C.
Figure 2008201911


実斜䟋、、のように、安定剀ずしおステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物を䜵甚するこずで、重金属を含有せず、か぀高枩環境䞋で粘着剀局の物性劣化がなく、たた糊残りの発生も防止できるマスキングテヌプが埗られた。

As in Examples 1, 2, and 3, by using calcium stearate, zinc stearate and a hydrotalcite compound as stabilizers, the physical properties of the pressure-sensitive adhesive layer are not deteriorated in a high temperature environment without containing heavy metals. There was obtained a masking tape that could prevent the occurrence of adhesive residue.

Claims (3)

ポリ塩化ビニル系基材の䞀方の面に、再剥離型粘着剀局が蚭けられたマスキングテヌプであっお、
前蚘ポリ塩化ビニル系基材が、ポリ塩化ビニルず、アゞピン酞ポリ゚ステル系可塑剀ず、熱安定剀ずしおのステアリン酞カルシりム、ステアリン酞亜鉛およびハむドロタルサむト系化合物を含むマスキングテヌプ。
A masking tape provided with a re-peelable pressure-sensitive adhesive layer on one surface of a polyvinyl chloride base material,
The masking tape in which the said polyvinyl chloride base material contains a polyvinyl chloride, an adipic acid polyester type plasticizer, and a calcium stearate, a zinc stearate, and a hydrotalcite type compound as a heat stabilizer.
前蚘アゞピン酞ポリ゚ステル系可塑剀の重量平均分子量が〜である請求項に蚘茉のマスキングテヌプ。   The masking tape according to claim 1, wherein the adipic acid polyester plasticizer has a weight average molecular weight of 500 to 2200. 再剥離型粘着剀局がアクリル系゚マルション型粘着剀からなる請求項たたはに蚘茉のマスキングテヌプ。   The masking tape according to claim 1, wherein the re-peelable pressure-sensitive adhesive layer is made of an acrylic emulsion-type pressure-sensitive adhesive.
JP2007039935A 2007-02-20 2007-02-20 Masking tape Pending JP2008201911A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2007039935A JP2008201911A (en) 2007-02-20 2007-02-20 Masking tape

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2007039935A JP2008201911A (en) 2007-02-20 2007-02-20 Masking tape

Publications (1)

Publication Number Publication Date
JP2008201911A true JP2008201911A (en) 2008-09-04

Family

ID=39779738

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007039935A Pending JP2008201911A (en) 2007-02-20 2007-02-20 Masking tape

Country Status (1)

Country Link
JP (1) JP2008201911A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010163484A (en) * 2009-01-13 2010-07-29 Lintec Corp Heat-resistant masking tape
WO2012121155A1 (en) * 2011-03-08 2012-09-13 日東電工株匏䌚瀟 Adhesive tape or sheet
JP2016194042A (en) * 2015-04-01 2016-11-17 日東電工株匏䌚瀟 Pressure-sensitive adhesive tape

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010163484A (en) * 2009-01-13 2010-07-29 Lintec Corp Heat-resistant masking tape
WO2012121155A1 (en) * 2011-03-08 2012-09-13 日東電工株匏䌚瀟 Adhesive tape or sheet
JP2012184369A (en) * 2011-03-08 2012-09-27 Nitto Denko Corp Self-adhesive tape or sheet
CN103502373A (en) * 2011-03-08 2014-01-08 日䞜电工株匏䌚瀟 Adhesive tape or sheet
JP2016194042A (en) * 2015-04-01 2016-11-17 日東電工株匏䌚瀟 Pressure-sensitive adhesive tape
JP2016194033A (en) * 2015-04-01 2016-11-17 日東電工株匏䌚瀟 Pressure-sensitive adhesive tape
CN108307638A (en) * 2015-04-01 2018-07-20 日䞜电工株匏䌚瀟 adhesive tape roll

Similar Documents

Publication Publication Date Title
JP5351400B2 (en) Removable adhesive sheet
CN104910824B (en) adhesive tape
TWI481689B (en) Pressure-sensitive adhesive sheet
KR101182944B1 (en) Removable Pressure Sensitive Adhesive Of Acrylic Emulsion Type And Method For Preparing The Same
EP2684924A1 (en) Adhesive tape or sheet
KR20150108771A (en) Adhesive tape or sheet for skin
CN105602463A (en) Pressure-sensitive adhesive sheet
JP4684686B2 (en) Re-peelable aqueous pressure-sensitive adhesive composition and decorative sheet
CN102149780A (en) Masking strip with a PVC film
JP6716222B2 (en) Wrapping film and processed products
WO2020137955A1 (en) Adhesive sheet
JP2008201911A (en) Masking tape
US6514606B2 (en) Pressure-sensitive adhesive sheet for skin adhesion and first-aid adhesive plaster using the same
JP2018165317A (en) Masking resin composition and masking sheet prepared therewith
KR101576688B1 (en) Pressure-sensitive adhesive composition for decorating panel, pressure-sensitive adhesive sheet and decorating panel
JP6344951B2 (en) Thermally conductive sheet and method for producing thermally conductive sheet
WO2020137956A1 (en) Protective sheet
WO2017150018A1 (en) Semiconductor processing sheet
KR101177248B1 (en) Removable Pressure Sensitive Adhesive Of Acrylic Emulsion Type And Method For Preparing The Same
KR101177249B1 (en) Removable Pressure Sensitive Adhesive Of Acrylic Emulsion Type And Method For Preparing The Same
JP2020105407A (en) Protective sheet
EP2557133A1 (en) PVC structures for adhesive applications
WO2021054215A1 (en) Emulsion-type adhesive and adhesive tape
JP2001302866A (en) Base film for pressure-sensitive adhesive sheet and method for producing the same
JP3096421B2 (en) Masking tape for painting