JPH0449544A - Magneto-optical disk - Google Patents
Magneto-optical diskInfo
- Publication number
- JPH0449544A JPH0449544A JP15749590A JP15749590A JPH0449544A JP H0449544 A JPH0449544 A JP H0449544A JP 15749590 A JP15749590 A JP 15749590A JP 15749590 A JP15749590 A JP 15749590A JP H0449544 A JPH0449544 A JP H0449544A
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- magneto
- optical disk
- bonding
- curing
- 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
Links
- 230000001070 adhesive effect Effects 0.000 claims abstract description 30
- 239000000853 adhesive Substances 0.000 claims abstract description 29
- 239000007788 liquid Substances 0.000 claims abstract description 27
- 239000000758 substrate Substances 0.000 claims abstract description 18
- 238000007348 radical reaction Methods 0.000 claims abstract description 11
- 239000003504 photosensitizing agent Substances 0.000 claims abstract description 5
- 229920000768 polyamine Polymers 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 8
- 150000002505 iron Chemical class 0.000 claims description 7
- 150000001451 organic peroxides Chemical class 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 1
- 239000000178 monomer Substances 0.000 abstract description 9
- 229920000642 polymer Polymers 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 3
- 239000004014 plasticizer Substances 0.000 abstract description 3
- 239000011521 glass Substances 0.000 abstract description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 9
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- -1 triethylamine Chemical compound 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- YNVZDODIHZTHOZ-UHFFFAOYSA-K 2-hydroxypropanoate;iron(3+) Chemical compound [Fe+3].CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O YNVZDODIHZTHOZ-UHFFFAOYSA-K 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000004831 Hot glue Substances 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 229920006332 epoxy adhesive Polymers 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 159000000014 iron salts Chemical class 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- KUFDRRWNPNXBRF-UHFFFAOYSA-N 1,4,8,12-tetrazacyclopentadecane Chemical compound C1CNCCCNCCNCCCNC1 KUFDRRWNPNXBRF-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- DZZAHLOABNWIFA-UHFFFAOYSA-N 2-butoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCC)C(=O)C1=CC=CC=C1 DZZAHLOABNWIFA-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- CKKQLOUBFINSIB-UHFFFAOYSA-N 2-hydroxy-1,2,2-triphenylethanone Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C(=O)C1=CC=CC=C1 CKKQLOUBFINSIB-UHFFFAOYSA-N 0.000 description 1
- DIVXVZXROTWKIH-UHFFFAOYSA-N 2-hydroxy-1,2-diphenylpropan-1-one Chemical compound C=1C=CC=CC=1C(O)(C)C(=O)C1=CC=CC=C1 DIVXVZXROTWKIH-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- QCPOKPFKMYZWBC-UHFFFAOYSA-N 2-octoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCCCCCC)C(=O)C1=CC=CC=C1 QCPOKPFKMYZWBC-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- PKBRCANVDCVQJP-UHFFFAOYSA-L iron(2+);propanoate Chemical compound [Fe+2].CCC([O-])=O.CCC([O-])=O PKBRCANVDCVQJP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- GUAWMXYQZKVRCW-UHFFFAOYSA-N n,2-dimethylaniline Chemical compound CNC1=CC=CC=C1C GUAWMXYQZKVRCW-UHFFFAOYSA-N 0.000 description 1
- JDEJGVSZUIJWBM-UHFFFAOYSA-N n,n,2-trimethylaniline Chemical compound CN(C)C1=CC=CC=C1C JDEJGVSZUIJWBM-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 229920002601 oligoester Polymers 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- ROEHNQZQCCPZCH-UHFFFAOYSA-N tert-butyl 2-tert-butylperoxycarbonylbenzoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1C(=O)OC(C)(C)C ROEHNQZQCCPZCH-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は一対の基板を貼り合わせて構成され、ビデオデ
ィスクやデジタルオーディオディスク、あるいは文書や
データのファイル用ディスクとして利用される密着貼り
合わせ型光磁気ディスクに係り、特に前記貼り合わせに
際して特定の接着剤を用いることにより、この部分に紫
外線等の光を照射して急速に硬化せしめて、まず貼り合
わせ面を仮固定し、これにより次の作業工程に移動可能
な状態を発現せしめ、次いで二液のラジカル反応により
硬化を完全に行い、この結果、貼り合わせ作業時間が極
度に短縮されるとともに貼り合わせが強固となり、かつ
加熱等の工程を必要とせずに低温で使用され、さらに情
報記録層を浸食せず、高信頼性を得る光磁気ディスクに
関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention is a close bonding type that is constructed by bonding a pair of substrates and is used as a video disc, digital audio disc, or document or data file disc. Regarding magneto-optical disks, in particular, by using a specific adhesive during the above-mentioned bonding, this part is irradiated with light such as ultraviolet rays and rapidly cured, first temporarily fixing the bonded surface, and then the next The material is made to be able to move during the work process, and then completely cured by a radical reaction between the two components.As a result, the bonding time is extremely shortened, the bond is strong, and processes such as heating are not required. The present invention relates to a magneto-optical disk that can be used at low temperatures without the need for information storage, does not erode the information recording layer, and has high reliability.
この種の光磁気ディスクは通常、一対の基板を貼り合わ
せて構成され、これらの貼り合わせ面の一方または両方
に情報記録層が設けられてなるものである。This type of magneto-optical disk is usually constructed by bonding a pair of substrates together, and an information recording layer is provided on one or both of these bonded surfaces.
この貼り合わせに当り、従来、エポキシ系接着剤、ウレ
タン系接着剤、紫外線硬化型接着剤、ホットメルト型接
着剤等の各種接着剤が用いられている。Conventionally, various adhesives such as epoxy adhesives, urethane adhesives, ultraviolet curing adhesives, and hot melt adhesives have been used for this bonding.
しかし、エポキシ系接着剤やウレタン系接着剤では硬化
速度が遅くて生産性に問題があり、紫外線硬化型接着剤
ではこの中に含有しているモノマー成分が基板や情報記
録層を浸食する恐れがあり、さらにホットメルト型接着
剤では耐熱性が低く、かつ接着強度に劣るという問題が
ある。However, epoxy adhesives and urethane adhesives have slow curing speeds, which poses productivity problems, and UV-curable adhesives have the risk of the monomer components contained therein corroding the substrate and information recording layer. Furthermore, hot melt adhesives have a problem of low heat resistance and poor adhesive strength.
特に近年、ISO規格に規定される80℃/85R)1
%で2000時間の耐久性が光磁気ディスクに要求され
るようになり、このため現状のホットメルトではこの要
求を満たし得ない。Especially in recent years, 80℃/85R)1 specified in the ISO standard
Magneto-optical disks are now required to have a durability of 2,000 hours in terms of 2000 hours, and current hot melts cannot meet this requirement.
そこで、本発明の目的は接着剤として特定のものを使用
することにより、この部分に紫外線等の光を照射して急
速に硬化せしめて、まず貼り合わせ面を仮固定し、これ
により次の作業工程に移動可能な状態を発現せしめ、次
いで二液のラジカル反応により硬化を完全に行い、この
結果、貼り合わせ作業時間が極度に短縮されるとともに
貼り合わせが強固となり、かつ加熱等の工程を必要とせ
ずに低温で使用され、さらに情報記録層を浸食せず、高
信頼性を確保し得、上述の公知技術に存する欠点を改良
した密着貼り合わせ型光磁気ディスクを提供することに
ある。Therefore, the purpose of the present invention is to use a specific adhesive, irradiate this area with light such as ultraviolet rays, and rapidly harden it, first temporarily fixing the bonded surface, and then use it for the next work. A state in which it can be transferred during the process is achieved, and then the two components are completely cured by a radical reaction. As a result, the bonding time is extremely shortened, the bonding becomes strong, and processes such as heating are not required. It is an object of the present invention to provide a closely bonded magneto-optical disk which can be used at low temperatures without corrosion, does not erode the information recording layer, can ensure high reliability, and has improved the drawbacks of the above-mentioned known techniques.
前述の目的を達成するため、本発明によれば、一対の基
板を貼り合わせて構成され、これら貼り合わせ面の少な
くとも一方の面に情報記録層が設けられた光磁気ディス
クにおいて、前記貼り合わせに際して有機過酸化物を含
むA液と、硬化促進剤を含むB液とからなる、ラジカル
反応により重合硬化する反応性二液型接着剤を用いるこ
とを特徴とし、かつ前記A液およびB液のいずれか一方
、または両方に光増感剤を含有せしめ、これらA1B液
を重ね合わせて、または混合して前記貼り合わせ面の一
方または両方の面に塗布し、次いでこの塗布部分に光を
照射して固着接合することを特特徴する。In order to achieve the above-mentioned object, according to the present invention, in a magneto-optical disk configured by bonding a pair of substrates together and having an information recording layer on at least one of the bonded surfaces, upon bonding, It is characterized by using a reactive two-component adhesive that polymerizes and cures by a radical reaction, consisting of a liquid A containing an organic peroxide and a liquid B containing a curing accelerator, and which is composed of a liquid A containing an organic peroxide and a liquid B containing a curing accelerator. One or both of them contains a photosensitizer, these A1B solutions are superimposed or mixed and applied to one or both of the bonded surfaces, and then this applied area is irradiated with light. It is characterized by a fixed bond.
以下、本発明を添付図面を用いて詳述する。Hereinafter, the present invention will be explained in detail using the accompanying drawings.
第1図は、本発明にかかる光磁気ディスクの分解図であ
って、プラスチック、ガラス等からなる一対の基板l、
1をラジカル反応による硬化機能と光照射による硬化機
能の両方を持ち備えた反応性二液型接着剤2を介して貼
り合わすことにより形成される。Aは一対の基板1.1
を貼り合わすことにより構成された本発明にかかる光磁
気ディスクの外観的斜視図である。FIG. 1 is an exploded view of a magneto-optical disk according to the present invention, which includes a pair of substrates l, made of plastic, glass, etc.
1 are bonded together via a reactive two-component adhesive 2 that has both a radical reaction-based curing function and a light irradiation-based curing function. A is a pair of substrates 1.1
1 is an external perspective view of a magneto-optical disk according to the present invention constructed by bonding together.
本発明に使用する反応性二液型接着剤において、A液は
メタアクリル酸エステル等の単量体およびオリゴマーを
主体とし、これに必要に応じて可溶性の重合体あるいは
可塑剤等を添加して均一溶液とし、この溶液100重量
部に対して有機過酸化物を0.1〜10重量部添加して
なるものである。このような有機過酸化物として具体的
には例えばベンゾイルパーオキサイド、ジ−t−ブチル
パーオキシフタレート、メチルエチルケトンパーオキサ
イド、t−ブチルハイドロパーオキサイド、クメンハイ
ドロパーオキサイド等が用いられる。In the reactive two-component adhesive used in the present invention, component A is mainly composed of monomers and oligomers such as methacrylic acid esters, to which a soluble polymer or plasticizer is added as necessary. A homogeneous solution is prepared by adding 0.1 to 10 parts by weight of an organic peroxide to 100 parts by weight of this solution. Specific examples of such organic peroxides include benzoyl peroxide, di-t-butyl peroxyphthalate, methyl ethyl ketone peroxide, t-butyl hydroperoxide, and cumene hydroperoxide.
また、B液は、メタアクリル酸エステル等の単量体およ
びオリゴマーを主体とし、これに必要に応じて可溶性の
重合体あるいは可塑剤等を添加して均一溶液とし、さら
にこの溶液100重量部に硬化促進剤を0.1〜5重量
部添加してなるものである。Liquid B is mainly composed of monomers and oligomers such as methacrylic acid ester, and if necessary, soluble polymers or plasticizers are added thereto to make a homogeneous solution, and then 100 parts by weight of this solution is added. It is made by adding 0.1 to 5 parts by weight of a curing accelerator.
前述において硬化促進剤はA液の重合硬化を促進するも
のであり、鉄塩と直鎖状ポリアミン類との配合液からな
る。該鉄塩と直鎖状ポリアミン類との配合比はモル比で
1:5〜1:400である。In the above description, the curing accelerator promotes polymerization and curing of liquid A, and is composed of a liquid mixture of iron salt and linear polyamines. The molar ratio of the iron salt to the linear polyamine is 1:5 to 1:400.
直鎖状ポリアミン類の比率が5より小さければ、接着力
が低下し、400よりも大であれば、硬化時間が長くな
るので、不適である。If the ratio of linear polyamines is less than 5, the adhesive strength will be reduced, and if it is more than 400, the curing time will be longer, which is unsuitable.
該鉄塩として、無機あるいは有機鉄塩があげられ、具体
的には、無水塩化第二鉄、硝酸第二鉄、乳酸鉄等である
。Examples of the iron salt include inorganic or organic iron salts, such as anhydrous ferric chloride, ferric nitrate, and iron lactate.
直鎖状ポリアミン類は一般式
(式中R+、 R2,Ra、R4はそれぞれ水素または
炭素数1〜8のアルキル基であり、nは1〜5の整数で
ある。)を有する化合物であり、具体的には、エチレン
ジアミン、ジエチレントリアミン、トリエチレンテトラ
ミン、テトラエチレンペンタミン、ペンタエチレンヘキ
サン等である。Linear polyamines are compounds having the general formula (wherein R+, R2, Ra, and R4 are each hydrogen or an alkyl group having 1 to 8 carbon atoms, and n is an integer of 1 to 5), Specifically, they include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexane.
前述の硬化促進剤はまた、鉄塩と環状ポリアミンとの配
合液であってもよい。この場合、該鉄塩と環状ポリアミ
ン類との配合比はモル比で1:1〜1:200である。The aforementioned curing accelerator may also be a liquid mixture of an iron salt and a cyclic polyamine. In this case, the molar ratio of the iron salt to the cyclic polyamine is 1:1 to 1:200.
環状ポリアミン類の比率が1よりも小さければ、接着力
が低下し、200よりも大であれば、硬化時間が長くな
るので、不適である。If the ratio of the cyclic polyamines is less than 1, the adhesive strength will be reduced, and if it is more than 200, the curing time will be longer, which is unsuitable.
該鉄塩としては前述と同様、無機あるいは有機鉄塩があ
げられ、具体的には、無水塩化第二鉄、硝酸第二鉄、乳
酸鉄等である。As mentioned above, examples of the iron salt include inorganic or organic iron salts, such as anhydrous ferric chloride, ferric nitrate, and iron lactate.
環状ポリアミン類は一般式
(式中、mlおよびm2はそれぞれ2〜8の整数であり
、nlおよびn、はそれぞれ0〜6の整数であってn+
+naが3以上であり、Xは1または2である。)有す
る化合物であり、具体的には、1.4,7.10−テト
ラアザシクロドデカン、1゜5.9.13−テトラアザ
シクロヘキサデカン、1゜4.8.11−テトラアザシ
クロテトラデカン、1゜4、 7.10.13.16−
ヘキサアザシクロオクタゾカン、1.4,8.12−テ
トラアザシクロペンタデカ、ン等である。Cyclic polyamines have the general formula (where ml and m2 are each an integer of 2 to 8, nl and n are each an integer of 0 to 6, and n+
+na is 3 or more, and X is 1 or 2. ), specifically, 1.4,7.10-tetraazacyclododecane, 1°5.9.13-tetraazacyclohexadecane, 1°4.8.11-tetraazacyclotetradecane, 1゜4, 7.10.13.16-
Hexaazacyclooctazocane, 1,4,8,12-tetraazacyclopentadecane, and the like.
さらに前述の硬化促進剤として、有機過酸化物とレドッ
クス系を形成する物質(レドックス系促進剤)を用いる
ことも出来る。このようなレドックス系促進剤としては
、例えばN、N’ ジメチルアニリン、N、N’ ジメ
チルトルイジン、トリエチルアミン等の第三級アミン類
、アルデヒドとアミンの縮合物、ナフテン酸コバルト、
プロピオン酸鉄などの金属石ケン類、有機金属錯体類、
チオ尿素又はその誘導体類などがある。Further, as the above-mentioned curing accelerator, a substance that forms a redox system with an organic peroxide (redox system accelerator) can also be used. Such redox promoters include, for example, N,N' dimethylaniline, N,N' dimethyltoluidine, tertiary amines such as triethylamine, condensates of aldehydes and amines, cobalt naphthenate,
Metal soaps such as iron propionate, organometallic complexes,
Examples include thiourea or its derivatives.
また、前述のA液、B液に於いて用いられる単量体は、
反応性モノマーであり、反応性モノマー類としては、メ
チルメタクリレート、2−ヒドロキシエチルメタクリレ
ート、2−ヒドロキシプロピメタルクリレート等のアク
リル酸エステルモノマー、メタクリル酸エステルモノマ
ーが用いられる。In addition, the monomers used in the above-mentioned liquids A and B are as follows:
It is a reactive monomer, and as the reactive monomers, acrylic acid ester monomers and methacrylic acid ester monomers such as methyl methacrylate, 2-hydroxyethyl methacrylate, and 2-hydroxypropimetal acrylate are used.
反応性オリゴマーとしては、ポリエーテルポリオールア
クリレート、ポリエーテルポリオールアクリレート、オ
リゴエステルアクリルレート等のアクリル又はメタクリ
ル系のオリゴマーが用いられ、同様にA液、B液に於い
て用いられる可溶性の重合体としては、アクリルエラス
トマー、SBR,NBR等の合成ゴム、及びABS、塩
化ビニル、PMMA、アルキッド樹脂等の合成樹脂等で
ある。As the reactive oligomer, acrylic or methacrylic oligomers such as polyether polyol acrylate, polyether polyol acrylate, and oligoester acrylate are used.Similarly, as the soluble polymers used in liquids A and B, , acrylic elastomer, synthetic rubber such as SBR, NBR, and synthetic resin such as ABS, vinyl chloride, PMMA, alkyd resin, etc.
本発明は前述のA液およびB液のいずれか一方、または
両方に光増感剤をAまたはB液100重量部に対して0
.5〜5重量部添加することを特徴とする。ここで、光
増感剤としては、例えばベンゾイン、ベンゾインメチル
エーテル、ベンゾインエチルエーテル、ベンゾインイソ
プロピルエーテル、ベンゾインブチルエーテル、ベンゾ
インオクチルエーテル、α−メチルベンゾイン、α−フ
ェニルベンゾイン、アセトフェノン、ベンゾフェノン等
のカルボニル化合物、ジフェニルスルフィド、ジフェニ
ルジスルフィド、ジチオカーバメート等の硫黄化合物、
アゾビスイソブチロニトリル、ヒドラゾン等のアゾ化合
物、その他金属カルボニルおよび色素類などがあげられ
る。In the present invention, one or both of the above-mentioned liquids A and B contains a photosensitizer at 0% per 100 parts by weight of liquid A or B.
.. It is characterized by adding 5 to 5 parts by weight. Examples of the photosensitizer include carbonyl compounds such as benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin butyl ether, benzoin octyl ether, α-methylbenzoin, α-phenylbenzoin, acetophenone, and benzophenone; Sulfur compounds such as diphenyl sulfide, diphenyl disulfide, dithiocarbamates,
Examples include azo compounds such as azobisisobutyronitrile and hydrazone, other metal carbonyls, and pigments.
本発明は前述のA液およびB液を重ねわせで、または混
合して貼り合わせ面に塗布し、次いでこの塗布部分に光
を照射して固着接合し、光磁気ディスクを貼り合わせる
。In the present invention, the above-mentioned liquids A and B are applied to the bonding surfaces in an overlapping manner or in a mixed manner, and then the coated areas are irradiated with light to firmly bond and bond the magneto-optical disks.
上述の貼り合わせをさらに具体的に述べれば、先ずアプ
リケーターによって該A液およびB液を混合した後、貼
り合わせ面に塗布し、貼り合わせ、若しくは、接合する
。この時点で、A液中の有機過酸化物は、B液中の反応
促進剤によって分解し、通常のラジカル反応によって重
合が進行するのであるが、その重合過程の初期、つまり
、接着剤が未硬化で、まだ流動するような段階で該接着
剤の露出部(表面)に光を照射すれば、光の当たる部分
については光によるラジカル反応も同時に進行すること
になり、特に光の照射エネルギーを加減することにより
、秒単位で当該部分を硬化せしめることが可能となり、
即ち極めて短時間に仮固定の状態に至らしめることがで
きる。又、最終的には上述の如き、重合開始剤によるカ
シカル重合も、完結することになり、完全な硬化・接着
が行われるものである。To describe the above-mentioned bonding more specifically, first, the A liquid and the B liquid are mixed with an applicator, and then applied to the bonding surface and bonded or bonded. At this point, the organic peroxide in Solution A is decomposed by the reaction accelerator in Solution B, and polymerization proceeds by a normal radical reaction. If the exposed part (surface) of the adhesive is irradiated with light while it is still flowing during curing, a radical reaction due to the light will also proceed at the same time in the exposed part, and in particular, the energy of the light irradiation will be reduced. By adjusting the amount, it is possible to harden the area in seconds.
In other words, it is possible to achieve a temporarily fixed state in an extremely short time. Furthermore, as described above, the radical polymerization by the polymerization initiator is also completed, and complete curing and adhesion are achieved.
A液、B液は、必ずしも混合して吐出する必要はなく、
A液、B液の重ね塗りに於いても全く同様の効果を有す
るものである。Liquid A and liquid B do not necessarily need to be mixed and discharged.
Exactly the same effect can be obtained even when the A liquid and the B liquid are overcoated.
なお、本発明において照射する光は、例えば光源からの
光を用いることができ、具体的には、水銀灯、キセノン
ランプ、ケミカルランプ又は、メタルハライドランプ等
が用いられる。Note that the light to be irradiated in the present invention can be, for example, light from a light source, and specifically, a mercury lamp, a xenon lamp, a chemical lamp, a metal halide lamp, or the like is used.
このようにしてなる本発明は使用する接着剤がラジカル
反応による硬化機能と光照射による硬化機能の両方を兼
ね備えてなるものであるので、貼り合わせ作業に要する
時間が極度に短縮され、かつ各部材の接合が強固である
。In the present invention, the adhesive used has both a radical reaction-based curing function and a light irradiation-based curing function, so the time required for bonding work is extremely shortened, and each member can be cured easily. The bond is strong.
第2図および第3図はそれぞれ本発明にかかる光磁気デ
ィスクの構成を表した断面図である。第2図および第3
図に示されるように、本発明にかかる光磁気ディスクA
は一対の基板1.1の貼り合わせ面1a、 laの少な
くとも一方の面、好ましくは両方の面に情報記録層3を
有し、この情報記録層3を保護膜4で覆った後、この保
護膜4上に反応性二液型接着剤2を介在させ、基板1.
1を貼り合わせることにより構成される。FIGS. 2 and 3 are cross-sectional views showing the structure of a magneto-optical disk according to the present invention, respectively. Figures 2 and 3
As shown in the figure, a magneto-optical disk A according to the present invention
has an information recording layer 3 on at least one surface, preferably both surfaces, of the bonded surfaces 1a and 1a of a pair of substrates 1.1, and after covering this information recording layer 3 with a protective film 4, this protective layer 3 is formed. A reactive two-component adhesive 2 is interposed on the film 4, and the substrate 1.
1 by pasting them together.
反応性二液型接着剤2は第2図に示されるように、基板
C1の両方の貼り合わせ面1a(実際には保護膜4の上
面)に塗布されてもよ(、また、第3図に示されるよう
にいずれか一方の面(片面)に塗布されてもよい。The reactive two-component adhesive 2 may be applied to both bonding surfaces 1a (actually, the upper surface of the protective film 4) of the substrate C1 as shown in FIG. It may be applied to either one side (single side) as shown in .
上述の本発明では、反応性二液型接着剤を用いて一対の
基板を貼り合わせたから、この反応性二液型接着剤の特
性により、この部分に紫外線等の光を照射して急速に硬
化せしめて、まず貼り合わせ面を仮固定し、これにより
次の作業工程に移動可能な状態を発現せしめ、次いで二
液のラジカル反応により硬化を完全に行い、この結果、
貼り合わせ作業時間が極度に短縮されるとともに貼り合
わせが強固となり、かつ加熱等の工程を必要とせずに低
温で使用可能であり、さらに情報記録層を浸食せず、高
信頼性をも確保できる。さらに、耐熱性、高接着強度を
も確保できる。すなわち、基板は光照射により位置ずれ
を防止するのに充分な初期接着力で数秒前後で仮固定さ
れ、その後接着剤は二液のラジカル反応により完全硬化
し、最終的には160℃以上の耐熱性と、充分な熱時強
度を発揮する。In the present invention described above, a pair of substrates are bonded together using a reactive two-component adhesive, so due to the characteristics of this reactive two-component adhesive, this area can be irradiated with light such as ultraviolet rays to rapidly cure. At the very least, the bonded surfaces are first temporarily fixed, thereby creating a state in which they can be moved to the next work process, and then completely cured by a radical reaction between the two components.As a result,
The bonding time is extremely shortened, the bond is strong, and it can be used at low temperatures without the need for heating or other processes. Furthermore, the information recording layer does not erode, ensuring high reliability. . Furthermore, heat resistance and high adhesive strength can also be ensured. In other words, the substrate is temporarily fixed in a few seconds by light irradiation with sufficient initial adhesive force to prevent positional displacement, and then the adhesive is completely cured by a radical reaction between the two components, and finally has a heat resistance of 160°C or higher. It exhibits excellent properties and sufficient strength when heated.
以上のとおり、本発明は一対の基板の貼り合わせに当り
、反応性二液型接着剤を用いたから、作業性、生産性が
向上することはもちろん、高信頼性をも確保でき、さら
に耐熱性に優れるとともに、高接着強度を確保でき、実
用上有用な発明である。As described above, since the present invention uses a reactive two-component adhesive to bond a pair of substrates together, it not only improves workability and productivity, but also ensures high reliability. This is a practically useful invention as it is excellent in adhesive properties and can ensure high adhesive strength.
第1図は本発明にかかる光磁気ディスクの分解図を示し
、第2図および第3図はそれぞれ、本発明にかかる光磁
気ディスクの断面図を示す。
1・・・基板、 1a・・・貼り合わせ面、2・・・
反応性二液型接着剤、
3・・・情報記録層、 4・・・保護膜、A・・・光
磁気ディスク。FIG. 1 shows an exploded view of a magneto-optical disk according to the invention, and FIGS. 2 and 3 each show a sectional view of the magneto-optical disk according to the invention. 1... Substrate, 1a... Bonding surface, 2...
Reactive two-component adhesive, 3... Information recording layer, 4... Protective film, A... Magneto-optical disk.
Claims (3)
合わせ面の少なくとも一方の面に情報記録層が設けられ
た光磁気ディスクにおいて、前記貼り合わせに際して有
機過酸化物を含むA液と、硬化促進剤を含むB液とから
なる、ラジカル反応により重合硬化する反応性二液型接
着剤を用いることを特徴とし、かつ前記A液およびB液
のいずれか一方、または両方に光増感剤を含有せしめ、
これらA、B液を重ね合わせて、または混合して前記貼
り合わせ面の一方または両方の面に塗布し、次いでこの
塗布部分に光を照射して固着接合することを特徴とする
密着貼り合わせ型光磁気ディスク。(1) In a magneto-optical disk constructed by bonding a pair of substrates and having an information recording layer provided on at least one of the bonded surfaces, during the bonding, a liquid A containing an organic peroxide and a curing It is characterized by using a reactive two-component adhesive that polymerizes and cures by a radical reaction, consisting of a B solution containing an accelerator, and a photosensitizer in either or both of the A solution and B solution. Contains,
A close bonding type characterized in that these A and B liquids are layered or mixed and applied to one or both of the bonded surfaces, and then the coated area is irradiated with light to firmly bond. magneto-optical disk.
前記硬化促進剤は鉄塩と直鎖状ポリアミンをモル比で1
:5〜1:400の比率で配合した配合液であり、該直
鎖状ポリアミンは次式の一般式を有する化合物である光
磁気ディスク。 ▲数式、化学式、表等があります▼ 式中R_1、R_2、R_3、R_4はそれぞれ水素ま
たは炭素数1〜8のアルキル基であり、nは1〜5の整
数である。(2) In the magneto-optical disk according to claim 1,
The curing accelerator contains iron salt and linear polyamine in a molar ratio of 1.
:5 to 1:400, and the linear polyamine is a compound having the following general formula. ▲There are mathematical formulas, chemical formulas, tables, etc.▼ In the formula, R_1, R_2, R_3, and R_4 are each hydrogen or an alkyl group having 1 to 8 carbon atoms, and n is an integer of 1 to 5.
硬化促進剤は鉄塩と環状ポリアミンとをモル比で1:1
〜1:200の比率で配合した配合液であり、該環状ポ
リアミンは次式の一般式を有する化合物である組立方法
。 ▲数式、化学式、表等があります▼ 式中、m_1およびm_2はそれぞれ2〜8の整数であ
り、n_1およびn_2はそれぞれ0〜6の整数であっ
てn_1+n_2が3以上であり、Xは1または2であ
る。(3) In the magneto-optical disk according to claim 1,
The curing accelerator is iron salt and cyclic polyamine in a molar ratio of 1:1.
An assembly method in which the cyclic polyamine is a compound having the following general formula: ▲There are mathematical formulas, chemical formulas, tables, etc.▼ In the formula, m_1 and m_2 are each an integer from 2 to 8, n_1 and n_2 are each an integer from 0 to 6, and n_1+n_2 is 3 or more, and X is 1 or It is 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15749590A JPH0449544A (en) | 1990-06-18 | 1990-06-18 | Magneto-optical disk |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15749590A JPH0449544A (en) | 1990-06-18 | 1990-06-18 | Magneto-optical disk |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0449544A true JPH0449544A (en) | 1992-02-18 |
Family
ID=15650934
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15749590A Pending JPH0449544A (en) | 1990-06-18 | 1990-06-18 | Magneto-optical disk |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0449544A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013227426A (en) * | 2012-04-25 | 2013-11-07 | Kaneka Corp | Two-component photo-curable composition |
-
1990
- 1990-06-18 JP JP15749590A patent/JPH0449544A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013227426A (en) * | 2012-04-25 | 2013-11-07 | Kaneka Corp | Two-component photo-curable composition |
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