JPH0411595B2 - - Google Patents

Info

Publication number
JPH0411595B2
JPH0411595B2 JP57203967A JP20396782A JPH0411595B2 JP H0411595 B2 JPH0411595 B2 JP H0411595B2 JP 57203967 A JP57203967 A JP 57203967A JP 20396782 A JP20396782 A JP 20396782A JP H0411595 B2 JPH0411595 B2 JP H0411595B2
Authority
JP
Japan
Prior art keywords
water
resin
synthetic resin
monomer ratio
soluble
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.)
Expired - Lifetime
Application number
JP57203967A
Other languages
Japanese (ja)
Other versions
JPS5993775A (en
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 filed Critical
Priority to JP20396782A priority Critical patent/JPS5993775A/en
Publication of JPS5993775A publication Critical patent/JPS5993775A/en
Publication of JPH0411595B2 publication Critical patent/JPH0411595B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Adhesives Or Adhesive Processes (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Laminated Bodies (AREA)
  • Adhesive Tapes (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

この発明は合成暹脂板甚衚面保護材に関する。 埓来より合成暹脂板は加工時、運送時、保管時
等においお、その衚面に疵が぀いたり、塵埃やシ
ダヌリング時の切粉が付着したりし易いため、合
成暹脂板の衚面を保護すべく皮々の衚面保護材が
提案され、䜿甚されおいる。䟋えばクラフト玙、
合成暹脂フむルムを基材ずし、これに合成暹脂系
たたはゎム系の感圧性接着剀を甚いお合成暹脂板
に貌着しおいる保護材がある。しかしながら䞊蚘
埓来の感圧タむプの保護材はコストが高く぀くほ
か、合成暹脂板に察する粘着力が匷すぎたり経日
倉化を起し易い。 たた最近では合成暹脂板補造のための成圢法ず
しお抌出成圢が倚く採甚されおいる背景からも抌
出暹脂板メタクリル板、ポリカヌボネヌト板、
ポリ塩化ビニル板、に察しお䞊蚘埓来の感圧タ
むプの保護材を甚いた堎合、板枩が原因で浮き皺
等を発生しお保護材ずしおの圹割を果しおいない
のが珟状である。なぜならば、抌出成圢されたラ
むン䞊の合成暹脂板の板枩は20°〜100℃たであ
り、䟋えば100℃にお感圧タむプの衚面保護材を
貌着した堎合、玙又はフむルムを基材ずするもの
では浮き状態ずなりシダヌリング時に合成暹脂板
の切粉が、浮いた保護材ず合成暹脂板間に入り蟌
み衚面疵の発生原因ずな぀たり、逆に匷く粘着し
すぎた個所では剥離䞍胜等が芋られ、衚面保護材
を䞀郚剥離しお板面に商暙等を印刷しようずする
堎合に困るものであ぀た。 玙又はフむルムを基材ずした埓来の感圧タむプ
の保護材は板枩60℃たでが限界であり、たた自己
粘着性タむプのフむルム補保護材も板枩が高い合
成暹脂板に察しお剥離困難、屋倖攟眮での経日倉
化が生じる。 さらに衚面保護材ずしおは玙又はフむルムを基
材ずし、氎貌りタむプの接着剀局を圢成したもの
もあるが、埓来品は抌出成圢された板枩の高い合
成暹脂板に察しお成圢ラむン䞊で䞀貫しお貌着す
るには板枩ずラむンスピヌドに適応し埗ず、䜿甚
し難いものであ぀た。 そこで、この発明においおは合成暹脂板甚衚面
保護材であ぀お氎貌りタむプずしお䜿甚できるず
共に、感圧タむプずしおも䜿甚可胜なものを提䟛
しようずしおおり、その構成は、玙による基材の
片面に䞋蚘のような(1)〜(5)の成分からなる氎分
散アクリル系暹脂ず、氎溶性暹脂ずを䞻成分ずし
お組成した接着剀局を圢成し、基材の他面にセラ
ツクレゞン、倉成セラツク等の倩然暹脂たたは、
フツ玠系合成暹脂による被芆局を圢成しおなるこ
ずを特城ずするものである。 (1) 〜12個の炭玠原子を含むアルキル基を有す
るアクリル酞又はメタクリル酞アルキル゚ステ
ルでモノマヌ比20〜80 (2) 個以䞋の炭玠原子を含むアルキル基を有す
るアクリル酞又はメタクリル酞アルキル゚ステ
ルでモノマヌ比20〜80 (3) グリシゞルアクリレヌト及びグリシゞルメタ
クリレヌトでモノマヌ比〜20 (4) アクリル酞又はメタクリル酞の−メチロヌ
ルアルキロヌルアミドでモノマヌ比〜20 (5) α−オレフむンカルボン酞でモノマヌ比〜
15 䜆し(3)(4)に぀いおは単独又は数皮適圓に組合せ
お䜿甚。次いでこの発明の衚面保護材に぀いお詳
现に説明するず、添付図面の第図第図に
おいお、はクラフト玙等の玙による基材、
は基材の片面に圢成しおある接着剀局であ
り、氎分散アクリル系暹脂10〜80重量ず氎
溶性暹脂10〜80重量ずを䞻成分ずし、これ
らに奜たしくは若干の柔軟付䞎剀〜10重量
ず消泡剀0.01〜0.1重量ずを組成した
もので、この接着剀局に蒞気又は氎スプレヌ
にお氎分を付䞎し、接着剀局を溶解しお合成
暹脂板に貌着するこずも可胜であるが、接着剀
局に蒞気又は氎スプレヌにお氎分を付䞎する
こずなく、そのたた感圧により合成暹脂板に貌
着するこずも可胜である。 䞊蚘接着剀局によるず、貌着䜿甚埌氎分が
気散された埌でも貌着性は付䞎されおいお、板枩
のある合成暹脂板に察しおも浮き皺発生、剥萜等
を起さない適床の粘着性による安定した粘着状態
を保有しおいる。即ち粘着性がなくなれば高枩板
での浮き皺の発生、剥萜が芋られる堎合が倚く、
たた粘着性が匷すぎるず剥離䞍胜の問題が発生す
るこずになるが、この発明による衚面保護材によ
るずこうした珟象の発生は芋られない。 さらに第図第図においお、は接着
剀局ずは反察偎になる基材の他面に圢成
したセラツクレゞン、倉性セラツク等の倩然暹脂
たたはフツ玠系合成暹脂による被芆局であ぀お、
該被芆局を圢成しおいるので、前蚘接着剀局
の氎分蒞発を抑制する䜜甚が倧きく䞔぀倖気
からの氎分をコントロヌルする䜜甚が加わり、接
着剀局をより安定化させる働きがある。即ち
被芆局の圢成にお衚面保護材ずしお合成暹脂
板に察する接着剀局の貌着状態をより安定
化させ、浮き皺の発生等を䞀局確実に阻止でき
る。 次に䞊蚘した接着剀局の䞻成分ずなる氎分
散アクリル系暹脂に぀いおは、 (1) 〜12個の炭玠原子を含むアルキル基を有す
るアクリル酞又は、メタクリル酞アルキル゚ス
テルでモノマヌ比20〜80 (2) 個以䞋の炭玠原子を含むアルキル基を有す
るアクリル酞又はメタクリル酞アルキル゚ステ
ルでモノマヌ比20〜80 (3) グリシゞルアクリレヌト又はグリシゞルメタ
クリレヌトでモノマヌ比〜20 (4) アクリル酞又はメタクリル酞の−メチロヌ
ルアルキロヌルアミドでモノマヌ比〜20 (5) α−オレフむンカルボン酞でモノマヌ比〜
15 〔䜆し(3)(4)に぀いおは単独又は適圓な組合せに
お䜿甚〕 䞊蚘(1)〜(5)の成分からなり゚マルゞペン重合
されたものからな぀おいる。埓぀お、その組合せ
方に぀いおは、(1)(2)(3)(5)(1)(2)(4)(5)(1)(2)(3
)(4)
(5)ずなる。 さらに䞻成分ずなる氎溶性暹脂ずしおは、 (1) ポリビニルアセテヌト郚分鹞化物、柱粉、デ
キストリン、れラチン、ポリビニルピロリド
ン、ポリ゚チレンオキサむト等の氎溶性高分子
からなる堎合ず (2) メチルセルロヌス、ヒドロキシ゚チルセルロ
ヌス、カルボキシ゚チルセルロヌスのアルカリ
塩等の氎溶性セルロヌス誘導䜓からなる堎合ず
がある。 そしお䞻成分ずしおの䞊蚘氎分散アクリル系暹
脂ず氎溶性暹脂ずの配合割合に぀いおは、粘着性
を有する範囲内であるこずが必芁で、詳现に぀い
おは埌述するが、氎分散アクリル系暹脂の各皮モ
ノマヌ重合比によ぀お倉わり埗るもので、ポリビ
ニルアルコヌルのブレンドにより粘着性が䜎䞋す
るこずを考慮しおブレンドするこずが必芁であ
る。 なお䞊蚘䞻成分ずなる氎分散アクリル系暹脂お
よび氎溶性暹脂ず、奜たしくは柔軟付䞎剀および
消泡剀ずを加える配合に぀いおは埌述の実斜䟋䞭
に明蚘した。 次に氎分散アクリル系暹脂䞻成分の暹脂組成に
぀いお䟋蚘するが前項蚘茉のモノマヌ比で重合さ
れ、通垞の゚マルゞペン重合ず同様にお行なわれ
る。その開始剀乳化剀等に぀いおは、垞法通りで
あり、限定されるものではなく特に前項蚘茉のモ
ノマヌ比であれば問題はないが、以䞋の凊方䟋に
お゚マルゞペン重合される。 −゚チルヘキシルアクリレヌト 43郚 ブチルアクリレヌト 30郚 −メチルロヌルアクリルアミド 郚 グリシゞルメタクリレヌト 郚 アクリル酞 郚 過硫酞カリ 0.5郚 NS−230日本油脂補 3.0郚 æ°Ž 120郚 〔重量郚〕 䞊蚘重合された゚マルゞペンに察し、さらに柔
軟付䞎剀、消泡剀等が添加されるもので、補造凊
方の具䜓䟋ずしおは、 〔重量比〕 氎分散アクリル系暹脂20〜60 10〜80 ポリビニルアセテヌト郚分鹞化物氎溶液 〜30 10〜80 グリセリン又はポリ゚チレングリコヌル 付加モル数200〜20000 〜10 消泡剀 0.01〜0.1 䞊蚘凊方による配合割合は粘着性を有する比率
であ぀おこれのみに限定されるものではない。た
た、ポリビニルアセテヌト郚分鹞化物は䞀般にポ
リビニルアルコヌルであ぀お、その鹞化量等によ
぀お物理的、化孊的な性質を異にするこずがあ
る。䞀般には 型  完党鹞化型 型  準完党鹞化型 型  郚分鹞化型 型  郚分鹞化型 重合床   重合床1500以䞊   重合床1000〜1500   重合床1000以䞋 メヌカヌによ぀お倚少衚瀺は異なるが䟋えば
GL−05は郚分鹞化型の重合床500である。 次に䞊蚘粘着材局ずは基材をはさんで反察
偎に圢成せられた被芆局に぀いおは、 (1) セラツクレゞン、倉性セラツクセラツクに
反応性シリコンを反応させたもの等の倩然暹
脂により圢成せられる堎合ず、 (2) フツ玠系合成暹脂により圢成せられる堎合ず
がある。 倩然暹脂䞭、被芆局ずしお倉性セラツクセラ
ツクに反応性シリコンを反応させたものを甚い
た堎合、キナアリングの䞍芁、颚也にお移行性を
生じない等の利点を有する。 たた被芆局をセラツクレゞンで圢成した堎合倚
数の有機溶剀に䞍溶等耐溶剀性が向䞊し、特にキ
ナアヌする必芁もなく、颚也にお移行性を生じな
い等の耐候性、耐油性も向䞊する。 䞀フツ玠系レゞンはアルコヌル系溶剀には可溶
であるが、それ以䞊の倚数の有機溶剀にはほずん
ど䞍溶であり、たたセラツクレゞンの堎合ず同
様、特にキナアヌする必芁もなく、颚也にお移行
性を生じない等の耐候性を有する。 䞊蚘したこの発明における衚面保護材ずしおの
特城は (1) 合成暹脂板メタクリル板、ポリカヌボネヌ
ト板、塩化ビニル板等の板枩が30〜100℃で
あ぀おも貌り合せが可胜である。 (2) 埓来の衚面保護材は板枩にお浮き皺が発生し
易いため、抌出成圢板の堎合、貌着スピヌドを
遅くするか、冷华板枩冷华装眮にお冷华し
おいるが、この発明の堎合には枩による圱響な
く貌着䜜業のスピヌドアツプをはかれるこずに
なる。 (3) この発明の堎合、前蚘のように浮き皺発生が
ないので衚面保護材を貌着したたたでシダヌリ
ングしおも切粉が衚面保護材ず合成暹脂板間に
入぀たりするおそれがない。 (4) この発明の堎合、基材に貌着埌、埌日印刷等
のため郚分的に剥離しおも再貌着が可胜な性質
を具有しおいる。 (5) 玙による基材の他面に倩然暹脂たたは合成暹
脂による被芆局が圢成されおいるため䞀局のこ
ず板枩に察する圱響を少なくし、衚面保護材の
保護機胜性の維持が高くなる。 (6) たた䞊述のような倩然暹脂あるいは合成暹脂
による被芆局の圢成は、特にキナアヌする必芁
もなく、垞枩におなしえる等加工容易である。 そしお良奜な剥離性を有し、耐油性、耐候性等
基材の物性をも向䞊させる。 以䞋この発明の実斜䟋に぀いお離型剀系統別に
比范䟋ず共に詳述する。 実斜䞊、40gcm2片艶クラフト玙の片面ザラ
面に倩然暹脂又は合成暹脂を塗垃し基材衚面
艶面に、各接着剀をコヌトしお衚面保護材ず
する。也燥埌堎合によ぀おは衚面保護材をそのた
た感圧により合成暹脂板に貌着するこずも可胜で
あるが、実斜䟋は也燥埌、合成暹脂板又は、保護
玙接着面に氎、蒞気スプレヌを付加し合成暹脂板
に衚面保護材を貌り合わせ、接着力、再接着力、
経日接着力、剥離埌の板面における糊残留性等に
぀いお詊隓した。 実斜䟋  被芆局はセラツクレゞンにお凊
理 氎分散アクリル系暹脂䞻成分 45 ポリビニルアルコヌルGL−05 50g グリセリン 5g SN−Deformer 154 0.1g 実斜䟋  被芆局はセラツクレゞンにお凊
理 氎分散アクリル系暹脂䞻成分 60g ポリビニルアルコヌルGL−05 35g グリセリン 5g SN−Deformer 154 0.1g 実斜䟋  被芆局はフツ玠系レゞンにお凊
理 氎分散アクリル系暹脂䞻成分 55g メチルセルロヌス 40 束本油脂䌚瀟補商品名マヌボロヌズ−25 ポリ゚チレングリコヌル200付加モル数200
5g SN−Deformer 154 0.1g 比范䟋  局はセラツクレゞンにお凊理 ポリビニルアルコヌルGL−05 95g ポリ゚チレングリコヌル200 付加モル数2005g NOPCO 8034 0.1g 比范䟋  被芆局はフツ玠系レゞンにお凊
理 ポリビニルアルコヌルGL−05 50g ポリビニルアルコヌルGH−17 45g グリセリン 5g NOPCO 8034 0.1g ※メチルセルロヌスの暹脂濃床は。 氎分散アクリル系暹脂䞻成分は暹脂濃床40。ポ
リ゚チレングリコヌル200、グリセリンは100
濃床。 ポリビニルアルコヌルGL−05は15濃床。 ポリビニルアルコヌルGH−17は15濃床。 NOPCO 8034、SN−Deformer 154はサンノブ
コ瀟の商品名である。
The present invention relates to a surface protection material for synthetic resin plates. Traditionally, synthetic resin boards have been prone to scratches on their surfaces, and dust and chips from shearing tend to adhere to them during processing, transportation, storage, etc., so various methods have been used to protect the surfaces of synthetic resin boards. Surface protection materials have been proposed and used. For example, kraft paper
There is a protective material that uses a synthetic resin film as a base material and adheres it to a synthetic resin plate using a synthetic resin-based or rubber-based pressure-sensitive adhesive. However, the above-mentioned conventional pressure-sensitive type protective materials are not only expensive, but also have too strong adhesion to synthetic resin plates and tend to deteriorate over time. In addition, extrusion molding has recently been widely adopted as a molding method for manufacturing synthetic resin boards, so extruded resin boards (methacrylic boards, polycarbonate boards,
Currently, when the above-mentioned conventional pressure-sensitive type protective material is used for a polyvinyl chloride board, it does not function as a protective material due to the occurrence of wrinkles and the like due to the board temperature. This is because the temperature of the synthetic resin board on the extrusion molding line ranges from 20°C to 100°C. For example, if a pressure-sensitive surface protection material is attached at 100°C, paper or film is used as the base material. If the protective material is adhered too tightly, it will become floating and during shearing, chips from the synthetic resin board will enter between the floating protective material and the synthetic resin board, causing surface flaws.On the other hand, if the adhesive is too strong, it may become impossible to remove it. This is problematic when attempting to print a trademark or the like on the board surface by partially peeling off the surface protection material. Conventional pressure-sensitive protective materials based on paper or film have a plate temperature limit of 60°C, and self-adhesive film protective materials are difficult to peel off from synthetic resin plates with high plate temperatures. , changes occur over time when left outdoors. Furthermore, some surface protection materials are made of paper or film as a base material and have a wet-type adhesive layer formed thereon, but conventional products are not suitable for extrusion-molded synthetic resin plates with high plate temperatures on the molding line. It was difficult to use because it could not adapt to board temperature and line speed for consistent adhesion. Therefore, the present invention aims to provide a surface protection material for synthetic resin boards that can be used as a water-applying type as well as a pressure-sensitive type. An adhesive layer composed mainly of a water-dispersed acrylic resin consisting of the following five components (1) to (5) and a water-soluble resin is formed, and a ceramic resin or a modified ceramic is applied to the other side of the base material. Natural resins such as
It is characterized by forming a coating layer of fluorine-based synthetic resin. (1) Acrylic acid or methacrylic acid alkyl esters having an alkyl group containing 6 to 12 carbon atoms with a monomer ratio of 20 to 80% (2) Acrylic acid or methacrylic acid having an alkyl group containing 5 or less carbon atoms Alkyl ester with a monomer ratio of 20-80% (3) Glycidyl acrylate and glycidyl methacrylate with a monomer ratio of 1-20% (4) N-methylolalkylolamide of acrylic acid or methacrylic acid with a monomer ratio of 1-20% (5) α -Olefincarboxylic acid with monomer ratio of 2~
15% However, (3) and (4) can be used alone or in an appropriate combination. Next, to explain the surface protection material of the present invention in detail, in FIG. 1 (FIG. 2) of the attached drawings, 10 is a paper base material such as kraft paper, 2 is a paper base material such as kraft paper, etc.;
0 is an adhesive layer formed on one side of the base material 10, which is mainly composed of a water-dispersed acrylic resin (10 to 80% by weight) and a water-soluble resin (10 to 80% by weight), and is preferably is composed of some softening agent (0 to 10% by weight) and antifoaming agent (0.01 to 0.1% by weight). Moisture is added to this adhesive layer 20 by steam or water spray, and the adhesive is Although it is possible to melt the layer 20 and adhere it to the synthetic resin plate P, it is also possible to apply pressure to the adhesive layer 20 without adding moisture to the adhesive layer 20 with steam or water spray, and to adhere it to the synthetic resin plate P as it is by pressure sensing. It is also possible to do so. According to the adhesive layer 20, the adhesion property is imparted even after moisture is diffused after use, and it does not cause floating wrinkles, peeling, etc. even on a synthetic resin board with a high board temperature. Possesses a stable adhesion state due to moderate adhesion. In other words, when the adhesiveness disappears, floating wrinkles and peeling are often observed on high-temperature plates.
Furthermore, if the adhesiveness is too strong, the problem of inability to peel occurs, but this phenomenon does not occur with the surface protection material of the present invention. Furthermore, in FIG. 1 (FIG. 2), 30 is a coating layer formed on the other surface of the base material 10 opposite to the adhesive layer 20 and made of natural resin such as ceramic resin, modified ceramic, or fluorine-based synthetic resin. It's hot,
Since the coating layer 30 is formed, it has a large effect of suppressing moisture evaporation in the adhesive layer 20 and also has an effect of controlling moisture from the outside air, thereby making the adhesive layer 20 more stable. That is, by forming the coating layer 30 as a surface protection material, the adhesion state of the adhesive layer 20 to the synthetic resin plate P can be more stabilized, and the occurrence of floating wrinkles can be more reliably prevented. Next, regarding the water-dispersed acrylic resin which is the main component of the adhesive layer 20 described above, (1) acrylic acid or methacrylic acid alkyl ester having an alkyl group containing 6 to 12 carbon atoms with a monomer ratio of 20 to 20; 80% (2) Acrylic acid or methacrylic acid alkyl ester with an alkyl group containing up to 5 carbon atoms with a monomer ratio of 20 to 80% (3) Glycidyl acrylate or glycidyl methacrylate with a monomer ratio of 1 to 20% (4) Acrylic N-methylolalkylolamide of acid or methacrylic acid with a monomer ratio of 1 to 20% (5) α-olefincarboxylic acid with a monomer ratio of 2 to 20%
15% [However, (3) and (4) may be used alone or in an appropriate combination] Consists of the five components (1) to (5) above, which are emulsion polymerized. Therefore, regarding the combination, (1)(2)(3)(5), (1)(2)(4)(5), (1)(2)(3
)(Four)
(5). Furthermore, the main component water-soluble resins include (1) those made of water-soluble polymers such as partially saponified polyvinyl acetate, starch, dextrin, gelatin, polyvinylpyrrolidone, and polyethylene oxide; and (2) methylcellulose, hydroxyethylcellulose, It may consist of a water-soluble cellulose derivative such as an alkali salt of carboxyethyl cellulose. The mixing ratio of the water-dispersed acrylic resin and the water-soluble resin as the main components must be within a range that maintains tackiness. This may vary depending on the polymerization ratio, and it is necessary to consider the fact that blending with polyvinyl alcohol reduces tackiness when blending. The formulation of the water-dispersed acrylic resin and water-soluble resin as the main components, and preferably the addition of a softener and an antifoaming agent, is specified in the examples below. Next, the resin composition of the main component of the water-dispersed acrylic resin will be exemplified. Polymerization is carried out at the monomer ratio described in the previous section, and carried out in the same manner as ordinary emulsion polymerization. The initiator, emulsifier, etc. are as usual and are not limited, but there is no problem as long as the monomer ratio is as described in the previous section, but emulsion polymerization is carried out in the following formulation example. 2-ethylhexyl acrylate 43 parts Butyl acrylate 30 parts N-methylol acrylamide 1 part Glycidyl methacrylate 2 parts Acrylic acid 4 parts Potassium persulfate 0.5 parts NS-230 (manufactured by NOF) 3.0 parts Water 120 parts [Parts by weight] The above polymerized A softening agent, antifoaming agent, etc. are added to the emulsion, and a specific example of the manufacturing recipe is as follows: [Weight ratio] Water-dispersed acrylic resin (20-60%) 10-80% Polyvinyl acetate Partially saponified aqueous solution (5-30%) 10-80% Glycerin or polyethylene glycol (number of moles added 200-20,000) 0-10% Antifoaming agent 0.01-0.1% The blending ratio according to the above formulation is a ratio that has tackiness. However, it is not limited to this only. Furthermore, partially saponified polyvinyl acetate is generally polyvinyl alcohol, and its physical and chemical properties may vary depending on the amount of saponification. In general, N type...completely saponified type A type...semi-completely saponified type G type...partially saponified type K type...partially saponified type Degree of polymerization H...degree of polymerization 1500 or more M...degree of polymerization 1000-1500 L... 
Degree of polymerization is 1000 or less The display may vary depending on the manufacturer, but for example
GL-05 is a partially saponified type with a degree of polymerization of 500. Next, regarding the coating layer 30 formed on the opposite side of the base material 10 from the adhesive layer, (1) a natural material such as ceramic resin or modified shellac (reactive silicone reacted with shellac); (2) In some cases, it is formed from a resin. (2) In some cases, it is formed from a fluorine-based synthetic resin. Among natural resins, when modified shellac (reactive silicone is reacted with shellac) is used as the coating layer, it has advantages such as no curing required and no migration during air drying. In addition, when the coating layer is formed of Ceramic resin, solvent resistance such as insolubility in many organic solvents is improved, there is no need for curing, and weather resistance and oil resistance such as no migration when air-dried are also improved. Fluorine-based resins are soluble in alcoholic solvents, but almost insoluble in many other organic solvents.Also, as with Ceramic resins, there is no need for special curing, and they are easily migrated by air drying. It has weather resistance such as not causing The features of the surface protection material according to the present invention described above are (1) It is possible to bond synthetic resin plates (methacrylic plates, polycarbonate plates, vinyl chloride plates, etc.) even when the plate temperature is 30 to 100°C. (2) Conventional surface protection materials tend to raise and wrinkle due to plate temperature, so in the case of extruded plates, the application speed is slowed down or the plate is cooled using a cooling (plate temperature cooling) device. In the case of this invention, it is possible to speed up the adhesion work without being affected by temperature. (3) In the case of this invention, as mentioned above, there is no floating wrinkles, so even if shearing is performed with the surface protection material attached, there is no risk of chips entering between the surface protection material and the synthetic resin board. . (4) In the case of the present invention, after being pasted on a base material, it has a property that it can be re-attached even if it is partially peeled off at a later date for printing or the like. (5) Since a coating layer of natural resin or synthetic resin is formed on the other side of the paper base material, the influence on plate temperature is further reduced, and the protective functionality of the surface protection material is maintained. (6) Furthermore, the formation of the coating layer using natural resin or synthetic resin as described above does not require curing and is easy to process, as it can be done at room temperature. It also has good releasability and improves the physical properties of the base material, such as oil resistance and weather resistance. Examples of the present invention will be described in detail below along with comparative examples for each type of release agent. In practice, a natural resin or synthetic resin is applied to one side (rough side) of 40g/cm 2 single-gloss kraft paper, and the base material surface (glossy side) is coated with each adhesive to serve as a surface protection material. After drying, depending on the case, it is possible to apply the surface protective material as it is to the synthetic resin board by pressure-sensing, but in this example, after drying, water or steam spray is applied to the adhesive surface of the synthetic resin board or protective paper. Adding surface protection material to the synthetic resin plate, adhesive strength, re-adhesion strength,
The adhesive strength over time, adhesive residue on the board surface after peeling, etc. were tested. Example 1 (Covering layer treated with Cerac resin) Water-dispersed acrylic resin main component 45g Polyvinyl alcohol GL-05 50g Glycerin 5g SN-Deformer 154 0.1g Example 2 (Covering layer treated with Cerac resin) Water-dispersed acrylic resin Main resin component 60g Polyvinyl alcohol GL-05 35g Glycerin 5g SN-Deformer 154 0.1g Example 3 (The coating layer is treated with fluorine-based resin) Water-dispersed acrylic resin main component 55g Methyl cellulose 40g (Product name manufactured by Matsumoto Yushi Company) Marboros M-25) Polyethylene glycol #200 (number of moles added: 200)
5g SN-Deformer 154 0.1g Comparative example 1 The layer is treated with Cerac resin) Polyvinyl alcohol GL-05 95g Polyethylene glycol #200 (added mole number 200) 5g NOPCO 8034 0.1g Comparative example 2 (The coating layer is treated with fluorine resin) Polyvinyl alcohol GL-05 50g Polyvinyl alcohol GH-17 45g Glycerin 5g NOPCO 8034 0.1g *The resin concentration of methylcellulose is 7%. The main component of water-dispersed acrylic resin has a resin concentration of 40%. Polyethylene glycol #200, glycerin is 100%
concentration. Polyvinyl alcohol GL-05 has a concentration of 15%. Polyvinyl alcohol GH-17 has a concentration of 15%. NOPCO 8034 and SN-Deformer 154 are product names of San Nobuco.

【衚】 ※ 備考 ○ 接着力枬定条件 20℃×60RH条件䞭、20時間攟眮埌枬定す
る。 接着力単䜍 100mmå·Ÿ 剥離速床 300mmmin 剥離角床 180°ピヌリング ○ 経日接着力 20℃×60RH条件䞋で90日攟眮埌の接着力 ○ 糊残留性 ○  糊残が芋られない合成暹脂板䞊に目芖
にお糊が残留しおいない ×  糊残が芋られる合成暹脂板䞊に目芖に
お糊が残留しおいる
[Table] * Note ○ Adhesive strength measurement conditions Measure after standing for 20 hours under 20℃ x 60%RH conditions. Adhesive strength unit: g/100mm width Peeling speed: 300mm/min Peeling angle: 180° peeling ○ Adhesive strength over time Adhesive strength after being left for 90 days at 20℃ x 60% RH ○ Adhesive strength ○...Adhesive residue is visible No (no visible glue remaining on the synthetic resin board) ×...Adhesive residue is visible (no visible glue remaining on the synthetic resin board)

【図面の簡単な説明】[Brief explanation of drawings]

図はこの発明の実斜態様を䟋瀺しおおり、第
図は断面図、第図は前図のものの䜿甚時の断面
図である。   基材、  接着剀局、  被
芆局、  合成暹脂板。
The figure illustrates an embodiment of the invention, the first
The figure is a sectional view, and FIG. 2 is a sectional view of the previous figure in use. 10...Base material, 20...Adhesive layer, 30...Coating layer, P...Synthetic resin plate.

Claims (1)

【特蚱請求の範囲】  玙による基材の片面に䞋蚘のような(1)〜(5)の
成分からなる氎分散アクリル系暹脂ず、氎溶性
暹脂ずを䞻成分ずしお組成した接着剀局を圢成
し、基材の他面にセラツクレゞン、倉成セラツク
等の倩然暹脂たたは、フツ玠系合成暹脂による被
芆局を圢成しおなるこずを特城ずする合成暹脂板
甚衚面保護材。 (1) 〜12個の炭玠原子を含むアルキル基を有す
るアクリル酞又はメタクリル酞アルキル゚ステ
ルでモノマヌ比20〜80 (2) 個以䞋の炭玠原子を含むアルキル基を有す
るアクリル酞又はメタクリル酞アルキル゚ステ
ルでモノマヌ比20〜80 (3) グリシゞルアクリレヌト及びグリシゞルメタ
クリレヌトでモノマヌ比〜20 (4) アクリル酞又はメタクリル酞の−メチロヌ
ルアルキロヌルアミドでモノマヌ比〜20 (5) α−オレフむンカルボン酞でモノマヌ比〜
15 䜆し(3)(4)に぀いおは単独又は数皮適圓に組合せ
お䜿甚。  氎分散アクリル系暹脂ず氎溶性暹脂ずを䞻成
分ずする接着剀局には若干の柔軟付䞎剀ず消泡剀
が加えられおいる䞊蚘特蚱請求の範囲第項蚘茉
の合成暹脂板甚衚面保護材。  氎溶性暹脂がポリビニルアセテヌト郚分鹞化
物、柱粉、デキストリン、れラチン、ポリビニル
ピロリドン、ポリ゚チレンオキサむト等の氎溶性
高分子からなる䞊蚘特蚱請求の範囲第項蚘茉の
合成暹脂板甚衚面保護材。  氎溶性暹脂がメチルセルロヌス、ヒドロキシ
゚チルセルロヌス、カルボキシ゚チルセルロヌス
のアルカリ塩等の氎溶性セルロヌス誘導䜓からな
る䞊蚘特蚱請求の範囲第項蚘茉の合成暹脂板甚
衚面保護材。
[Scope of Claims] 1. An adhesive layer composed mainly of a water-dispersed acrylic resin consisting of the following five components (1) to (5) and a water-soluble resin on one side of a paper base material. 1. A surface protection material for a synthetic resin plate, characterized in that a coating layer is formed on the other side of the base material by a natural resin such as ceramic resin or modified ceramic, or a fluorine-based synthetic resin. (1) Acrylic acid or methacrylic acid alkyl esters having an alkyl group containing 6 to 12 carbon atoms with a monomer ratio of 20 to 80% (2) Acrylic acid or methacrylic acid having an alkyl group containing 5 or less carbon atoms Alkyl ester with a monomer ratio of 20-80% (3) Glycidyl acrylate and glycidyl methacrylate with a monomer ratio of 1-20% (4) N-methylolalkylolamide of acrylic acid or methacrylic acid with a monomer ratio of 1-20% (5) α -Olefincarboxylic acid with monomer ratio of 2~
15% However, (3) and (4) can be used alone or in an appropriate combination. 2. The surface for a synthetic resin board according to claim 1, wherein a small amount of a softening agent and an antifoaming agent are added to the adhesive layer mainly composed of a water-dispersed acrylic resin and a water-soluble resin. Protective layer. 3. The surface protection material for a synthetic resin board according to claim 1, wherein the water-soluble resin is a water-soluble polymer such as partially saponified polyvinyl acetate, starch, dextrin, gelatin, polyvinylpyrrolidone, or polyethylene oxide. 4. The surface protection material for a synthetic resin board according to claim 1, wherein the water-soluble resin is a water-soluble cellulose derivative such as methylcellulose, hydroxyethylcellulose, or an alkali salt of carboxyethylcellulose.
JP20396782A 1982-11-19 1982-11-19 Surface protecting material for synthetic resin plate Granted JPS5993775A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20396782A JPS5993775A (en) 1982-11-19 1982-11-19 Surface protecting material for synthetic resin plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20396782A JPS5993775A (en) 1982-11-19 1982-11-19 Surface protecting material for synthetic resin plate

Publications (2)

Publication Number Publication Date
JPS5993775A JPS5993775A (en) 1984-05-30
JPH0411595B2 true JPH0411595B2 (en) 1992-02-28

Family

ID=16482601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20396782A Granted JPS5993775A (en) 1982-11-19 1982-11-19 Surface protecting material for synthetic resin plate

Country Status (1)

Country Link
JP (1) JPS5993775A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62101836U (en) * 1985-12-13 1987-06-29
JPS62221531A (en) * 1986-03-24 1987-09-29 名叀屋油化株匏䌚瀟 Surface coating material
JPH0359342U (en) * 1989-10-13 1991-06-11

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55124654A (en) * 1979-03-19 1980-09-25 Nitto Electric Ind Co Preparation of sheet* whose surface is protected
JPS5770162A (en) * 1980-10-20 1982-04-30 Toagosei Chem Ind Co Ltd Acrylic repeelable adhesive

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56111144U (en) * 1980-01-28 1981-08-27

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55124654A (en) * 1979-03-19 1980-09-25 Nitto Electric Ind Co Preparation of sheet* whose surface is protected
JPS5770162A (en) * 1980-10-20 1982-04-30 Toagosei Chem Ind Co Ltd Acrylic repeelable adhesive

Also Published As

Publication number Publication date
JPS5993775A (en) 1984-05-30

Similar Documents

Publication Publication Date Title
JP2832565B2 (en) Automotive coating protection sheet
KR100382846B1 (en) Pressure Sensitive Adhesive Sheet
JPS62129374A (en) Releasable pressure-sensitive adhesive and its production
CN101484545A (en) Adhesive sheet
JPH09157627A (en) Water-soluble tacky adhesive agent composition
JPH0321681A (en) Photopolymerizing pressure- sensitive adhesive
US4753846A (en) Adhesive compositions for use on vinyl substrates
JPH0246626B2 (en) GOSEIJUSHIITAYOHYOMENHOGOZAI
JPH0411595B2 (en)
US4892917A (en) Adhesive compositions for use on vinyl substrates
US3931444A (en) Backing sheet coated with catalyst and self curing interpolymer adhesive
JP4885374B2 (en) Wet surface adhesive adhesive
JPH08174773A (en) Pressure-sensitive adhesive for laminated tile carpet and tile carpet to which it is applied
JPH04202393A (en) Adhesive composition
JPS617369A (en) Adhesive composition
JP2000129224A (en) Decorative pressure-sensitive adhesive sheet
JP3848448B2 (en) Adhesive composition and surface protective film or sheet using the same
JPS62121053A (en) Surface protective sheet
JP2010070609A (en) Easily re-pastable adhesive tape
JPH0670144B2 (en) Adhesion method for processed plastic products
JP3511522B2 (en) Adhesives and their uses
JPH0240711B2 (en) GOSEIJUSHIITAYOHYOMENHOGOZAI
JPH05229069A (en) Production of surface protected resin panel
JPS62243670A (en) Adhesive
JPH09286080A (en) Surface protecting film