JPS601273A - Radiation-curing pressure-sensitive adhesive composition - Google Patents
Radiation-curing pressure-sensitive adhesive compositionInfo
- Publication number
- JPS601273A JPS601273A JP10976883A JP10976883A JPS601273A JP S601273 A JPS601273 A JP S601273A JP 10976883 A JP10976883 A JP 10976883A JP 10976883 A JP10976883 A JP 10976883A JP S601273 A JPS601273 A JP S601273A
- Authority
- JP
- Japan
- Prior art keywords
- radiation
- dithiol
- reaction product
- diacrylate
- oligomer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polymerisation Methods In General (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、薗い俊果力と候盾′註の1!!nた放列勝峻
化型感圧牲按盾剤組底吻に関了ゐ〇従来、感圧性の粘虐
テープ類において、phwの凝集力、接増力などの接涜
%憔忙発揮丁/bために、比較的高分子量、尚粘度の皿
台体(つまり、天然ゴム、合成ゴム前)に使用する必女
があった。このため、塗工の餘、巾伽浴卸J中におけゐ
俗准の状態として基材上に塗布しなけiLはならない。[Detailed Description of the Invention] The present invention is characterized by its great agility and strength! ! In the past, in pressure-sensitive viscous tapes, phw cohesive force, multiplication force, etc. Therefore, it was necessary to use it for plate bases with relatively high molecular weight and viscosity (that is, before natural rubber or synthetic rubber). For this reason, during coating, iL must be applied onto the substrate in a standard manner during the bathing process.
しかしながら、使用した人員の浴卸]に蒸発させ/)た
め、塗布俊の乾燥工程e(長時間弛必女と丁ゐ0しかも
、1配目的に使用される浴剤は揮発性であって燃えや丁
く、人体に悪影覧を及は丁ものか多いから、その1史用
力・しはししよ、火災発生の原因となったり%独々の公
告問題τ引き2こ丁、また、柱彼旧見地、並ひに、上6
1公害防止上の観点力・ら、その収直か不可避とされる
沼剤回収装置は、−飯に高1jbであって、かつ収備的
に人@h@i%忙必をとする0そこで。However, due to the drying process of the application (necessary long-term relaxation), the bath additives used for this purpose are volatile and flammable. In fact, there are many things that can cause negative effects on the human body, so one of them is that it can cause a fire, and the other is that it is a public notice issue of its own. Hashira He Old Viewpoint, Namihini, Part 6
1. From the perspective of pollution prevention, the swamp agent recovery equipment that is considered unavoidable is extremely expensive and requires a lot of people to collect. Therefore.
咋年いわゆる、省貴諒、省エネルギー、および無公否化
という児地力・ら感圧接涜剤の無浴創化4コ注目さ扛て
米た。無浴剤化対策として、エマルジョン型、ホットメ
ルト型などかめるが1%に歇状オリゴマー葡利用した放
射線硬化型感圧住徽廂剤が脚光才あびている。その理由
に、放射勝硬化型感圧性接腐剤では、前述の浴欣型感圧
性接治創の入点である有機浴剤オ原則として含んでいな
い、いわゆる無浴削化がiiJ能であり、あるいは含ん
でも少量であること、ざらに(1)姑住エネルギ線であ
る放射解忙用いるため、硬化(1台)反応か早い;(2
)硬化反応か進行丁ゐため、ボッドライフの調節が自由
に出来ゐ;(5)製造の際、太@な乾燥P葡必蛍としな
い;などの待e葡もっていゐためで必ゐ。ところか、こ
の放射側硬化型感圧・註接層沖]の場せでも、以下の難
点があな。つ丑り、一般にルせ(硬化)反応は放射勝照
痢候、発生したラジカルにより、小飽和二産結せへと進
行丁ゐが、反応速度か早く過剰に朱檎しやすい。(結果
としてカラス転移点か上昇する。)−f:れゆえ、形成
した皮膜はもろく、他端な場合、車台収縮か太きくキレ
ツτ生ずな。この状態の皮膜時性に訓べゐと、大きな破
〜[強匿に竹するが、伸びはほとんどなく、ゴム的住買
葡ボざない。一方過剰の朱橘忙仰飼丁ゐため、分子内の
小飽和二亜結台の杷対鼠に誠ら丁と局所的に反工し、が
進行して、全体としては光分な献果力か狗らrL&い結
果となる。In the 18th century, Riki Koji and others attracted attention to the four types of pressure-sensitive sanitizing agents that are known for their value-saving, energy-saving, and non-public use. As a countermeasure for eliminating bath additives, radiation-curing pressure-sensitive stimulants that use 1% mitotic oligomers, such as emulsion type and hot melt type, are gaining attention. The reason for this is that radiation-curing pressure-sensitive adhesives do not, in principle, contain organic bath agents, which are the key to the bath-type pressure-sensitive wound treatment described above, making them so-called bath-free. , or even if it does contain a small amount, (1) the curing reaction is fast (1 unit) because it uses radiation decoupling, which is an energy ray; (2)
) Since the curing reaction is progressing, the body life can be adjusted freely; (5) During production, it is necessary to avoid drying too thickly. However, even with this radiation-side hardened pressure-sensitive layer, there are the following drawbacks. In general, the russet (hardening) reaction progresses to a low saturation reaction due to the generated radicals, but the reaction rate is too fast and it is easy to cause excessive oxidation. (As a result, the glass transition point rises.) -f: Therefore, the formed film is brittle, and in the other case, the chassis shrinks and thick cracks τ occur. If you learn about the properties of the film in this state, there will be a big break. On the other hand, due to the excessive amount of Zhu Citrus, there is a local reaction between the loquats and the rats of the small saturated two-dimensional structure in the molecule, which progresses and gives a light result as a whole. It's a powerful result.
以上のように、硬化反応を通#に制御し、感圧性抜屑酌
としての接酒狩性τ維付丁勺ことは離刀・しい状況にあ
った。そこで1本発明省らは特開1155−27511
号公報にs 7rX丁ように、ビニル基を有丁ゐ化合9
1jK多官能チオ一ル化合物に添加丁ゐことにより、放
射線によって良好に硬化し、市い#呆力と接盾性に肩丁
ゐことπ見出し提条した0刀・\ゐ組成’l’/Jか、
長打な依盾カン与えゐ坤田の肝鵬は、明らかではないか
。As described above, it is difficult to fully control the curing reaction and use a pressure-sensitive waste extractor to remove the liquid. Therefore, the Ministry of Invention et al.
As shown in the publication No. s 7r
By adding a 1jK polyfunctional thiol compound, it is well cured by radiation, and the composition 'l'/ J?
Isn't it obvious that Ikonden's key point is to give him long-hitting shots?
多′自tjbチオール化合物のSH希の放射杵t%応注
か篩いこと、′!またビニル基とSH基の反LL、がビ
ニル基とビニル糸の連鎖n台的戊応と競合しており、そ
の粕来映化物の架偏点間距離か艮〈なゐものと推定され
ゐ。Multi-tjb thiol compound SH rare radiation pestle t% pouring or sieving,'! In addition, the anti-LL of the vinyl group and the SH group competes with the chain reaction of the vinyl group and the vinyl thread, and it is presumed that the distance between the eccentric points of the kasurai film is different. .
しかしなから、このようなテスー−ル化8吻π含む組成
物よ!71ゐ粘盾創の揚せ、放射線により光分に硬化さ
せて噂)、悌かではあるか、チオール時雨−の不快臭忙
勺丁心といった問題がめった。そこで、さらに鋭意饋死
忙慮ねた鮎米、ジチオールとジアクリレートモノマとの
反五巳、物を使用丁nは、前−欠点か贋決さnゐことて
見い出し5本発明に刊達した。However, it is a composition containing such a tessellated 8 π! Problems such as 71゜ sticky wounds (rumored to have been hardened by radiation) and the unpleasant odor of thiols were common. Therefore, we have made further efforts to investigate the use of ayu-mai, dithiol, and diacrylate monomers, and have finally published the present invention under the heading 5. .
本発明は、良好l放射線硬化11及び接渚力忙巾し、チ
オール化合物t(ありかちな不快7I−英気のない粘右
剤9c提供丁ゐものであめ。The present invention provides good l radiation curing 11 and sanding power, and thiol compounds (commonly unpleasant 7I - dull viscosity 9c).
丁lわ°ら、本発明に、ラジカル朱橋性エナレン性不記
・11に里粕8を分子内に・8丁ゐ放射綜級化型故状オ
リゴマー100M坑郁に対して、ジチオールとジアクリ
レートモノマと葡反比、芒せてなる化合9Aτ0.5〜
60皇i都言M1−勾ことにl特徴とする放射線硬化型
Iバ出性徽崩剤組成物であめ。In the present invention, we have added dithiol and dithiol to the 100M reactor of the radical-linked enalene. Acrylate monomer and inverse ratio, compound 9Aτ0.5~
60 Koitogen M1 - A radiation-curing type I-releaseable disintegrating agent composition characterized by the following characteristics:
本発明のml成?7において、姫力りするジチオールと
ジアクリレートモノマの反ふし、させてなる化89勿に
ついてH己丁と以Fの辿りとなな0つ1す。ml composition of the present invention? In 7, the reaction of the dithiol and the diacrylate monomer that binds the dithiol and the reaction of the diacrylate monomer result in a chemical reaction.
ジチオールの不快臭は、台数時の未反応めゐいは加水分
解した。41酉nヒテオールと宥えらKLゐ0そこで、
そのチオール葡一般に、水洗なとにより狛製し−C1除
去丁ゐが光分でlい0また、チオールはビニル糸q守に
アクロイル基と反応1註か良好でろ/)0以上の結果、
シナオール1モルに対してジアクリレートモノマイ0.
1〜1モル50℃〜120’Cで2時間以上均一に1W
件しなから、反応させ1面分子片化丁ゐと。The unpleasant odor of dithiol was caused by hydrolysis in the unreacted portions. There,
The thiol is generally made into a mold by washing with water, and the C1 removal rate is 10% by light.Also, the thiol reacts with the acroyl group on the vinyl thread.The result is 0 or more.
0.0% diacrylate monomer per mole of cinnaol.
1 to 1 mol 1W uniformly for 2 hours or more at 50℃ to 120'C
Therefore, it is possible to react and fragment the molecules on one side.
化合9/Jは5反応俊および放射勝照射欽もほとんど不
快臭オ壱しないこと忙見出した。It has been found that Compound 9/J has almost no unpleasant odor even after 5 reactions and irradiation.
X発明の鮒戚切においては、狗らnゐ粘燈テーフー類の
% 1nll上、放射1除硬化型敵状オリゴマー100
沖−車首15vc又」して上す已ジチオールとジアクリ
レートモノマの戊比、物で0.5〜60厘魚都用いるこ
とか灯よしいOo、5庫昂部禾44ではほとんど効朱か
なく、また60星稙部に越χなと。In the carp cutting of the invention
The ratio of dithiol and diacrylate monomer is 0.5 to 60 liters, which is good when using 0.5 to 60 liters of water. , I also met 60 Hoshi Tanabe.
# ’j’l 腺fj!l! 化性スジ;a−r−−ず
−6M I用スフ’ h 6 。# 'j'l gland fj! l! Curable streaks; a-r-zu-6M I stripes' h 6 .
A弁明において用いりことかでさゐ○ジチオールとして
は、レリえはエタノジチオール、ブタンシナオール、ヘ
キザメナレンシナオール、テカンメテレンジナオール、
エチレンクリコールビス(チオグリコレート)、エチレ
ンクリコール(β−メル〃フトフロヒオイート9ヘキサ
ンジオールテオグロビオイ・−ト青かあけらnる0藍り
、シアタリレートモノマとしては、エチレンクリコール
シアタリレート、テトラエテレングリコールジアクリレ
ート、1.6−ヘキサングリコールジアクリレート、ネ
オペンナルグリコールジアクリレート、エチレングリコ
ールジメタクリレート、1.6−ヘキサングリコールジ
アクリレート、ビスメタタリルオキシエナルンオスフエ
イト(レリえはE1丞化朱■衷KAYAMEj<PM−
2)、ポリエステルジアクリレート(8本化楽旧讐製曲
品名MANI)A)寺かめゐ。The dithiols used in A's defense include ethanodithiol, butansinaol, hexamenalensinaol, tecanmetherenedinaol,
Ethylene glycol bis(thioglycolate), ethylene glycol (β-merophthaloyl ester 9-hexane diol teoglobioate), cyatarylate monomer, ethylene glycol Recall siatarylate, tetraethene glycol diacrylate, 1,6-hexane glycol diacrylate, neopennal glycol diacrylate, ethylene glycol dimethacrylate, 1,6-hexane glycol diacrylate, bismethatharyloxyenalunosph Eight (Relie is E1 丞圱■衷KAYAMEj<PM-
2) Polyester diacrylate (manufactured by 8-piece manufacturer MANI) A) Terakamei.
次VC2t−,元明vCおr)ゐ分子内Vcフジカルq
す偏性エナレン性小胞′)flに厘結台9c市する放射
載映化型e、秋オリゴマとしては、玉鎖かアクリル畝ア
ルキルエステルあるいは、メタクリル咳アルキルエステ
ルイ低M台度に共座せしたオリゴマtはじめ、ポリオー
ルアクリレート、ポリエステルアクリレート、ウレタン
アクリレート、エポキシアクリレートなどの小胞4にM
帖台忙1勺子あたり1個以上木端あるいは狽り知にtつ
アクリル糸オリゴマ、さらにポリブタジェン、ホリクロ
ログレン、ポリインブレン寺の反工6性の2レホリマで
あるOLへそのオリゴマは敵状で、無俗剤であって、溶
剤忙使用しても少血である〇ざらにその粘度としては常
渦で10’cps〜5X106cpsの組曲であな。Next VC2t-, Genmei vC or) Intra-molecular Vc physical q
The obligate enallenoid vesicle') fl has a radiation-mounted type e, which is attached to the 9c, and the fall oligomer is a bead, an acrylic ridge alkyl ester, or a methacrylic ridge alkyl ester. M in vesicles 4 such as oligomers, polyol acrylate, polyester acrylate, urethane acrylate, and epoxy acrylate.
At least one acrylic thread oligomer per 1 strand of wood or twigs, as well as polybutadiene, polychlorogrene, and polyimbrin 2-reformer oligomers, which are 6 types of anti-corrosion oligomers, are hostile. It is a vulgar drug, and even if you use a solvent, it will cause a small amount of blood.The viscosity of the drug is 10'cps to 5x106cps in a normal vortex.
なお本発明に:h−いて時に好ましい結果が侍らnゐの
は反応性の商いアクリル糸の二皿結せ忙付与した万すゴ
マである。また、さらにこの放射腕硬化型液状オリゴマ
に枯漕付与剤忙刀Dλゐlす、史に心安に紀1して軟化
々1ハ敵化防止剤。In addition, in the present invention, the preferred result can be obtained by using a reactive acrylic thread with two threads tied together. In addition, this radial arm hardening type liquid oligomer is added with a drying agent Dλ, which is an anti-fog agent for softening and softening.
光積ハ1」、願′4−+なとτ混入丁ゐ礪せがめゐ。Mitsubishi HA 1'', request'4-+ and τ are mixed in.
A元ゆ」でいう放封寸綜とは、γ占注工不ルキー籾で、
α軸、β線、1勝、中1住子蔵、カロ連′亀十勝のよ′
)な竜維注故射巌並びに紫タシ勝τいう。箪喘陛飲豹綜
の場せの線型は、0.5〜50 Mradの軛囲T″l
1lj川できゐか、好ましくは1〜2゜M r a d
程度でめる0ま/’C紫タシタ1勝台、約780 nm
〜460 nmの波艮郵囲で1発生Wとしてr、h部上
の水銀ランプ寺か卒けらrL/)。また揚台によっては
硬化促進創(紫外線の礪せは増都創)を言上さ一+!:
ることもできゐが照射丁ゐ楠せ、鉤に注意忙要丁ゐ点は
照射雰−気である。っlす、発生したシジカルか望気中
のば索によって朗害避nゐので、揚台によるでは窒系な
との小活性カスで直換さrL心が、皮展上tフィルム寺
で被憶しても艮い。The ``Amotoyu'' refers to ``Gamma Zhanjuko Furuki'' rice,
α-axis, β-ray, 1 win, 1st year of junior high school, Sumikozo, Karo Ren ``Kame Tokachi no Yo''
) Na Ryūwei Shūsha Igan and Murasaki Tashikatsu τ. The linear shape of the drinking leopard ridge is 0.5 to 50 Mrad.
1 lj river, preferably 1~2° M r a d
0ma/'C Murasaki Tashita 1-win stand, approximately 780 nm
A wave of ~460 nm is generated in a range of 1 to 100 nm (W) and a mercury lamp on the r, h section (rL/). Also, depending on the lifting platform, hardening of the wound may be accelerated (ultraviolet rays may cause fading of the wound). :
It is also possible to do so, but the key point is the irradiation atmosphere. However, since the generated cysicals or airborne fibers can avoid harmful effects, the core is directly exchanged with a small amount of active gas such as nitrogen based on the lifting platform, and the core is covered with a film on the skin. It doesn't matter if I remember it.
以F、実施VIJ9cもって胱明丁ゐOlお、以下にお
いて都とあるのは血亀部忙ボ丁0
実抛例1、比軟例1,2゜
a)市分子倉チオール化8物のせ成
撹拌依、渦紋ば11 注入目τ督した6つロフラスコに
1.6−ヘキサンシオールジナオンロヒオネート1モル
イしこみ、60℃葦で昇藺丁ゐ。仄いで、での温度に抹
ちなから、攪拌し、e末の1.6ヘキサンジ万一ルシア
タリレー)0.5モルに徐々に60分力・けて注入し、
終了域、80°C筐で昇温し、6時間株繍1反尾、させ
て、無色巧明な菌分子量チオール化せ物τ(0たO
b)放射腋硬化型故状オリゴマーの甘酸アクリル赦ブチ
ル80都、グリシジルメタクリレート20sに触媒の存
在下で塊状Mせ葡竹ない、無俗剤のアクリル糸共産台体
に8成した。得らf′した故状オリゴマーの厘搬平均分
子亀は約5.11 ’00、粘度は2 X I D’c
ps(60°C)であった0次いで、アクリル鈑に10
部付〃U反応させ、狽1j炉に不縮第1二虚鮎甘葡付っ
たアクリル糸の放射艇硬化型敵状オリゴマτ8成した。Hereinafter, with implementation VIJ9c, the term ``capital'' refers to ``blood turtle''. Stir and vortex 11 Pour 1 mole of 1,6-hexanethioldinaonrochionate into a 6-bottle flask and heat at 60°C. Because it was a little fuzzy and the temperature did not change, it was stirred and gradually poured into 0.5 mol of 1.6 hexane difluoride (e) for 60 minutes.
At the end of the process, the temperature was raised to 80°C in a cabinet, and the strain was incubated for 6 hours. In the presence of a catalyst, 80% butyl and 20s of glycidyl methacrylate were used to form a lumpy mass of grapevine bamboo into an acrylic yarn composite body. The average molecular weight of the obtained oligomer f' is approximately 5.11'00, and the viscosity is 2 X I D'c.
ps (60°C), then 10 on the acrylic plate.
A radiation-curing type oligomer τ8 of acrylic thread was formed by reacting with the acrylic thread and attaching the unshrinkable first and second imaginary sweet potatoes to the furnace.
以上のようVCC甘心f′した2臼ノゴマ一100部に
ヌ」してS a)で台ノ戊した尚分子員チオール化せ敏
1τ20都励力1して、放射蛛硬化型感圧性法虐剤粕成
物πft−成した。仄に比軟νす1として、上述のチオ
ール化付物τ旨まlいオリゴマー単独1
9C組by、吻に選ひ、比軟例2としてはa)の化合物
V(代えて)゛クンジチオール忙10酢刀nえlcもの
τ組成物に遇ひ、反膜彎性の比軟に竹なった。As mentioned above, we added 100 copies of VCC's 2000 pieces to 100 copies of VCC, and then used the thiolated member 1 τ 20 and expelled 100 copies in S a). A drug residue product πft- was prepared. As a relatively soft example 1, the above-mentioned thiolated adduct τ tasty oligomer alone 19C group is selected as the snout, and as a relatively soft example 2, the compound V of a) (instead of) ``cundithiol'' I encountered the τ composition of the 10th grader NLC, and it became bamboo with a softer antimembrane curvature ratio.
皮膜げ、−f:れそれの組峨吻オシリコーン処坤し7’
1lfW#に一定厚み(?J 1 [11111) 俸
布シ、最大)JIJ連電圧電圧21vleV嶽褒圧指型
篭子勝)JIJ連器(EBG)によV%全索雰囲気下(
取紫龜度400p戸)で1発生させた電子腺1mAで1
0M r a d照付1丁ゐことにより、爪台。網状化
させて、1手IJ又した。Film removal, -f:Resore no assembly silicone treatment 7'
1lfW# constant thickness (?
1 electronic gland generated at 1 mA at 400p
0M rad with 1 light and a nail stand. I made it into a mesh and did one IJ again.
そして、そn−t’nの皮膜にテンシロン引労・2試験
恢で伸び率、破師f5虫度ン測定した。幀朱は衣1の則
りであったOな吃・、引り1ナリ速吸は200mm/分
(20°C)である。Then, the elongation rate and breakage rate f5 of the film were measured using Tensilon tension test and 2 tests. Horiaki was according to the rule of clothing 1, and the pulling speed was 200 mm/min (20°C).
衣1皮膜有性
実施?lJ 1の組W、物は元号、ゴム的性看忙ボ丁こ
とがわかったので、次にそrLぞnの組成物音0.02
5mm厚のポリエステルフィルム(東しく一製5曲品名
、ルミラー$25)K抜溝剤層の厚みか0.015mm
K1心ように塗布し、前述と同様に電子巌葡照荊し、接
漕力、M巣力を両足した0
結果に表2にボす。Clothes 1 film sexual implementation? lJ 1's group W, the thing is the era name, and I found out that it is a rubber sex nurse bocho, so next I will write the composition sound of sorLzon 0.02
5mm thick polyester film (Toshikuichi 5-piece product name, Lumirror $25) Thickness of K groove removal agent layer: 0.015mm
Apply the same coating to the K1 core, apply the electron beam as described above, and add the contact force and M force to the results, which are shown in Table 2.
表2 粘瘤テーグの特・注比較
注) IIJIS−C−2107KllLで測定(扱*
犀: SUS 450 BA板)2165℃の力D#1
1Jll:進試彫d日山J葡竹lい俵宥力のヱ冒力11
オ%でボした0
(壇加か少ないはと艮好)
3)ベータライト板にて何里51]Og 、 20℃で
60分段のす7′L、距離τ測知C
粕来より、チオールによる不快美もなく、一定の嵯集力
忙待ち、経時変化の少ない粘看テープでめゐ刀為ら1%
性の優itた感圧性依潰剤であゐことは明ら〃・である
。Table 2 Comparison of special and custom made viscous Teig
Rhinoceros: SUS 450 BA plate) 2165℃ force D#1
1 Jll: Shinshibori d Hiyama J Sochiku l Tawara Appeasement's Evolving Power 11
3) How many miles on the beta light board 51] Og, 60 minutes at 20℃ Step 7'L, distance τ measurement C From Kasurai, There is no unpleasant appearance caused by thiol, and the adhesive tape has a certain concentration and little change over time.
It is clear that it is a pressure-sensitive crushing agent with superior properties.
実施例2.比較Vす5
C)商分子諏ナオール化せ二吻の合成
実施?l11のa)と同様な装置により、デカンメチレ
ンジチオール1モルとテトラエチレングリコールアタリ
レート0,5モル忙反応させて合成した。Example 2. Comparison Vsu5 C) Synthesis of commercial molecule sulnaolization of two proboscises? Synthesis was carried out by reacting 1 mole of decane methylene dithiol with 0.5 mole of tetraethylene glycol arylate using the same apparatus as in a) of 111.
d)液状オリゴマー〇せ敢
アクリル咳エテル10都、アクリル散ブチル70台hメ
タタリル敵ダリシジル20Hi+塗実施?lJ 1と同
様に、!甘し、その俊、アクリルM10部付加させて、
アクリル糸の放射餓映化B1〆に状オリゴマ9c台戟し
た。d) Liquid oligomer 〇 10 units of acrylic cough ether, 70 units of acrylic powder, h 20 Hi+ application of metataryl enemy darisidil? Similar to lJ 1,! Sweet, Sono Shun, let me add 10 copies of acrylic M.
The acrylic yarn was radiated into B1 and the oligomer 9c was used.
次にこのオリゴマーにC)のチオール化8物會20部茄
加して放射緻映化型感圧性俊庸削組成vlJ葡作成した
。次に比較νす6として1)の・チオール化合収1の代
りに、デヵンメテレンジテオールオ泗び 10 都深加
して組成物としたO
そnぞnの組成物〒0.06mm厚のポリエチレンフィ
ルムに、鑑庸剤層の厚みか0.006mmKなるように
塗布し、リニアフィラメント型の電子線照射に匣(En
ergy 5cience Inc。Next, 20 parts of the thiolated 8 compound C) was added to this oligomer to prepare a radiation-imaging pressure-sensitive agility composition vlJ. Next, as a comparison v6, instead of 1) thiol compound yield 1, decanemethane ditheol was added and 10% of the composition was prepared. It was coated on a polyethylene film with a thickness of 0.06 mm so that the thickness of the identification agent layer was 0.006 mmK, and a box (En) was applied to the linear filament type electron beam irradiation.
ergy 5science Inc.
I!A曲品名エレクトロカーテンンで加速′電圧165
kv、ビーム電冗5 mA 2用い、望系雰囲気下(酸
2#Us o oppm)で5Mradの電子線照射し
1表囲保餓用の枯后フィルムτ製埴し、特性の#’F
′iun 91:イ丁7.z−+;io (表6ン表5
枯涜フィルム将狂としての比較
4) 枯眉フィルム忙貼f1けたSO8仮τJISB7
777Vc準じテ、8IllI′lIエリクセン絞9π
イ丁ない室崗1日恢のフィルムの自然剥離状態τ観祭。I! A song name Acceleration with electrocurtain voltage 165
Using a beam electric current of 5 mA and 2 mA, 5 Mrad electron beam irradiation was performed in a positive atmosphere (acid 2 # Us o oppm) to form a drying film τ for surface preservation, and the characteristic #'F was obtained.
'iun 91: i-cho 7. z−+;io (Table 6 Table 5
Comparison as a dry film general 4) dry eyebrow film busy paste f1 digit SO8 provisional τJISB7
Same as 777Vc, 8IllI'lI Eriksen diaphragm 9π
A look at the natural peeling state of the film after one day of use.
表6より、不快莫もなく、帷時笈化の少ない絞υ性も艮
好な表■抹暎用枯眉フィルムであめことがわかった。From Table 6, it was found that the dry eyelash film for eyelids was free of discomfort and had good squeezing properties with less curling.
以上のよシに本発明によ扛は1分士内に小飽オロニ虚結
台τ肩する放射線硬化型散状オリゴマーにシナオールと
アルキル貼オキサイドとの反応生j戊物τ麻力1丁ゐこ
とtζよジ、不快臭のない商いl!従振力と接層時1王
のしtt7ζI翳出性按膚創π提供すゐことが内油とな
った。As described above, according to the present invention, a reaction product of cinnaol and an alkyl-attached oxide to a radiation-curable dispersed oligomer, which has a small amount of imaginary condensation within 1 minute, can be produced. This is a trade without unpleasant odors! When the vibrational force and the contact with the layer were applied, it became the inner oil to provide the tt7ζI exposed skin wound.
−W2O−-W2O-
Claims (1)
子内に1丁ゐ放射勝硬化型敵状オリゴマ100崖輩郡に
対し、シナオール1モルにジアクリレートモノマτ0.
1〜1モル)y、1乙、させてなゐ化合吻忙0.5〜6
0皇重都含南丁ゐことτ鉤ばと丁ゐ放射勝硬化型感出注
恢腐酌組成物。1. For 1 mole of cinnaol and 1 mole of cinnaol and 0.00 diacrylate monomer per 1 mole of radical-containing ethylenically unsaturated organic nail lees and 100 units of radiation-curing enemy oligomer in the molecule.
1 to 1 mole) y, 1 mol, 0.5 to 6
A radiation-curing type sensitized injection molding composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10976883A JPS6020427B2 (en) | 1983-06-17 | 1983-06-17 | Radiation-curable pressure-sensitive adhesive composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10976883A JPS6020427B2 (en) | 1983-06-17 | 1983-06-17 | Radiation-curable pressure-sensitive adhesive composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS601273A true JPS601273A (en) | 1985-01-07 |
JPS6020427B2 JPS6020427B2 (en) | 1985-05-22 |
Family
ID=14518734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10976883A Expired JPS6020427B2 (en) | 1983-06-17 | 1983-06-17 | Radiation-curable pressure-sensitive adhesive composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6020427B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63196680A (en) * | 1987-02-12 | 1988-08-15 | Hitachi Chem Co Ltd | Radiation-curable pressure-sensitive adhesive composition |
US4891152A (en) * | 1987-12-28 | 1990-01-02 | Hughes Aircraft Company | Dispersion of liquid crystal droplets in a photopolymerized matrix and devices made therefrom |
US5278199A (en) * | 1990-01-12 | 1994-01-11 | Asahi Denka Kogyo K.K. | Actinic radiation-reactive pressure-sensitive adhesive composition wherein adhesiveness is reduced upon irradiation |
-
1983
- 1983-06-17 JP JP10976883A patent/JPS6020427B2/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63196680A (en) * | 1987-02-12 | 1988-08-15 | Hitachi Chem Co Ltd | Radiation-curable pressure-sensitive adhesive composition |
US4891152A (en) * | 1987-12-28 | 1990-01-02 | Hughes Aircraft Company | Dispersion of liquid crystal droplets in a photopolymerized matrix and devices made therefrom |
US5278199A (en) * | 1990-01-12 | 1994-01-11 | Asahi Denka Kogyo K.K. | Actinic radiation-reactive pressure-sensitive adhesive composition wherein adhesiveness is reduced upon irradiation |
US5360873A (en) * | 1990-01-12 | 1994-11-01 | Asahi Denka Kogyo K.K. | Actinic radiation-reactive pressure-sensitive adhesive composition |
Also Published As
Publication number | Publication date |
---|---|
JPS6020427B2 (en) | 1985-05-22 |
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