TW574339B - Adhesive composition for optical disks - Google Patents

Adhesive composition for optical disks Download PDF

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Publication number
TW574339B
TW574339B TW90119903A TW90119903A TW574339B TW 574339 B TW574339 B TW 574339B TW 90119903 A TW90119903 A TW 90119903A TW 90119903 A TW90119903 A TW 90119903A TW 574339 B TW574339 B TW 574339B
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Taiwan
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composition
meth
scope
acrylate
patent application
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TW90119903A
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Chinese (zh)
Inventor
Atsuya Takahashi
Masakatsu Ukon
Takayoshi Tanabe
Takashi Ukachi
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Jsr Corp
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J4/00Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/252Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
    • G11B7/256Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers improving adhesion between layers

Description

574339 A7 __B7 五、發明説明(1 ) 發明領域 (請先閲讀背面之注意事項再填寫本頁} 本發明有關一種可感光固化之組合物。此外,本發明 有關該組合物作爲供光碟使用之膠黏劑的用途。 背景 經濟部智慧財產局員工消費合作社印製 由電腦技術、電腦軟體技術、及通訊技術所代表之資 訊技術的最近發展使得可在高速下傳輸更多資料。如此一 來,則需要且發展了可在高密度下記錄更多資料之記錄媒 體。就該種高密度記錄媒體而言,D V D (數位式影像磁 碟或數位式多用途磁碟)已發展成爲下一世代之通用型記 錄媒體。D V D通常係藉著接合兩片磁碟而製得,因此需 要膠黏劑以黏著該兩磁碟。習用膠黏劑之實例係包括熱熔 性膠黏劑、熱可固化性膠黏劑、厭氣固化性膠黏劑。然而 ,此等習用膠黏劑具有各種缺點。例如,熱熔性膠黏劑具 有較差之熱安定性及耐候性,因此在高溫下軟化,導致磁 碟因爲膠黏性降低而分離或變形。而且,難以施加熱熔性 膠黏劑於具有作爲記錄膜之半透明薄膜的雙層D V D上, 因爲該熱熔性膠黏劑之透明性較差。熱可固化膠黏劑之問 題在於形成磁碟之基材在固化期間因熱而變形。或者,若 使用較低溫度,則固化該膠黏劑需要長周期之時間。厭氣 固化性膠黏劑具有較差之產能,因爲固化該膠黏劑需要較 長周期之時間。已有人提出光可固化之膠黏劑以解決此等 問題。例如,日本專利公開申請案編號1 4 2 5 4 5 / 1 9 86及編號8946 2/1 9 94揭示紫外光UV — -4 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 _ B7 五、發明説明(2 ) (請先閲讀背面之注意事項再填寫本頁} 可固化之樹脂膠黏劑’其含有胺基甲酸酯丙烯酸酯之主要 組份。然而,此等紫外光U V -可固化密度膠黏劑在磁碟 邊緣的固化性、對於形成半透明薄膜之黃金的膠黏性、耐 濕熱性及其類性質無法令人滿意。是故,本發明之目的係 提出一種供光碟使用之紫外光U V -可固化樹脂組合物, 其磁碟邊緣具有改良之固化性。 此外,本發明之目的係提出一種對於黃金或其類材料 之膠黏性改善之樹脂組合物。 此外,本發明之目的係提出一種在與習用膠黏劑比較 之下,具有改良之耐濕熱性的組合物。 發明槪述 經過徹底硏究的結果,本發明者發現前述目的可藉著 組合輻射-可固化寡聚物與以下組份(B )及/或(C ) 及(D )而達成。 經濟部智慧財產局員工消費合作社印製 是故,本發明提出一種組合物,其包含 (A )輻射可固化之寡聚物,以胺基甲酸酯(甲基) 丙烯酸酯爲佳,其可藉多元醇化合物、聚異氰酸酯化合物 、及含有羥基之(甲基)丙烯酸酯化合物進行反應而製得 ,及 (B )二烷基胺基苯甲酸酯。 此外,本發明提出一種組合物,其包含 (A )輻射可固化之寡聚物,以胺基甲酸酯(甲基) 丙烯酸酯爲佳,其可藉多元醇化合物、聚異氰酸酯化合物 -5- 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 574339 A7 ___B7 五、發明説明(3 ) 、及含有羥基之(甲基)丙烯酸酯化合物進行反應而製得 9 (請先閲讀背面之注意事項再填寫本頁) (C )(甲基)丙烯酸羥基烷酯,及 (D)至少一種選自包括2,2 —二甲氧基一 1 ,2 —二苯基乙一 1 一酮、2 -羥基—2 -甲基一 1 一苯基丙 - 1 -酮、及1 -羥基環己基苯基酮之群的化合物。574339 A7 __B7 V. Description of the invention (1) Field of invention (please read the notes on the back before filling out this page) The present invention relates to a photocurable composition. In addition, the present invention relates to the composition as a glue for optical discs. The use of adhesive. Background The recent development of information technology represented by computer technology, computer software technology, and communication technology printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs has enabled more data to be transmitted at high speeds. A recording medium capable of recording more data at a high density is needed and developed. As for such a high-density recording medium, a DVD (digital video disk or digital versatile disk) has been developed for the next generation Type recording media. DVDs are usually made by joining two magnetic disks, so an adhesive is needed to adhere the two magnetic disks. Examples of conventional adhesives include hot-melt adhesives, heat-curable adhesives Adhesives, anaerobic curable adhesives. However, these conventional adhesives have various disadvantages. For example, hot-melt adhesives have poor thermal stability and weather resistance. Therefore, it softens at high temperature, causing the magnetic disk to separate or deform due to reduced adhesiveness. Moreover, it is difficult to apply a hot-melt adhesive to a double-layer DVD having a translucent film as a recording film because of the hot-melt The adhesive has poor transparency. The problem with heat-curable adhesives is that the substrate forming the magnetic disk is deformed by heat during curing. Or, if a lower temperature is used, it takes a long time to cure the adhesive. . Anaerobic curable adhesives have poor productivity because curing the adhesive requires a longer cycle time. Light-curable adhesives have been proposed to solve these problems. For example, Japanese Patent Laid-Open Application No. 1 4 2 5 4 5/1 9 86 and number 8946 2/1 9 94 Reveal ultraviolet light UV — -4-This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) 574339 A7 _ B7 V. Invention Note (2) (Please read the precautions on the back before filling out this page} Curable resin adhesive 'it contains the main component of urethane acrylate. However, these ultraviolet light UV-curable density Adhesive in The curability of the edge of the disc, the adhesiveness to the gold forming the translucent film, the heat and humidity resistance, and other properties are not satisfactory. Therefore, the object of the present invention is to propose a UV-curable ultraviolet light for optical discs. The resin composition has improved curability at the edge of the magnetic disk. In addition, the object of the present invention is to provide a resin composition having improved adhesion to gold or the like. In addition, the object of the present invention is to provide a resin composition Compared with conventional adhesives, the composition has improved moisture and heat resistance. The invention has been thoroughly studied, and the inventors have found that the foregoing object can be achieved by combining a radiation-curable oligomer with the following components ( B) and / or (C) and (D). Therefore, the present invention proposes a composition containing (A) radiation-curable oligomer, preferably urethane (meth) acrylate, which can It is prepared by reacting a polyol compound, a polyisocyanate compound, and a (meth) acrylate compound containing a hydroxyl group, and (B) a dialkylaminobenzoate. In addition, the present invention provides a composition comprising (A) a radiation-curable oligomer, preferably a urethane (meth) acrylate, which can be borrowed from a polyol compound, a polyisocyanate compound-5- This paper size is in accordance with Chinese National Standard (CNS) A4 (210 X 297 mm) 574339 A7 ___B7 5. Description of the invention (3), and (meth) acrylic acid compounds containing hydroxyl groups are reacted to obtain 9 (please first (Please read the notes on the back and fill in this page) (C) At least one kind of hydroxyalkyl (meth) acrylate, and (D) selected from the group consisting of 2,2-dimethoxy-1, 2-diphenylethyl-1 1 Compounds of the group of ketones, 2-hydroxy-2-methyl-1,1-phenylpropan-1-one, and 1-hydroxycyclohexylphenyl ketone.

本發明組合物較佳係包含所有四種組份(A ) - ( D )° 本發明進一步提出該組合物作爲供光碟使用之膠黏劑 的用途,例如數位式多用途磁碟。 而且,本發明提出一種光碟,例如數位式多用途磁碟 ,其包含可藉著固化本發明組合物而製得之膠黏劑。 發明詳述 經濟部智慧財產局員工消費合作社印製 作爲組份(A )之寡聚物可爲任何適當之輻射可固化 寡聚物,例如(甲基)丙烯酸酯寡聚物。較佳組份(A ) 係爲胺基甲酸酯(甲基)丙烯酸酯寡聚物,其可藉著多元 醇化合物、聚異氰酸酯化合物、及含有羥基之(甲基)丙 烯酸酯化合物進行反應而製得。 就多元醇化合物而言,可使用聚醚多元醇、聚酯多元 醇、聚碳酸酯多元醇、聚己內酯多元醇、分子中具有兩個 或多個羥基之脂族烴、分子中具有兩個或多個羥基之脂環 族烴、分子中具有兩個或多個羥基之不飽和烴、及其類者 。此等多元醇可個別或兩種或多種組合使用。 -6- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 Α7 Β7 五、發明説明(4 ) 聚醚多元醇之實例有脂族聚醚多元醇、脂環族聚醚多 元醇、及芳族聚醚多元醇。 (請先閲讀背面之注意事項再填寫本頁) 脂族聚醚多元醇之實例有聚乙二醇、聚丙二醇、聚丁 二醇、聚己二醇、聚庚二醇、聚癸二醇、異戊四醇、二異 戊四醇、三羥甲基丙烷;多羥醇諸如氧化烯加成多元醇諸 如氧化乙烯加成三元醇之三羥甲基丙烷、氧化丙烯加成三 元醇之三羥甲基丙烷、氧化乙烯/氧化丙烯加成三元醇之 三羥甲基丙烷、氧化乙烯加成四元醇之異戊四醇、及氧化 乙烯加成六元醇之二異戊四醇;藉兩種或多種離子可聚合 之環狀化合物進行開環聚合所製得之聚醚多元醇;及其類 者。 經濟部智慧財產局員工消費合作社印製 離子可聚合之環狀化合物之實例有環醚諸如氧化乙烯 、氧化丙烯、丁烯一 1 一氧化物、氧化異丁烯、3,3 -雙(氯曱基)氧雜環丁烷、四氫呋喃、2 -甲基四氫呋喃 、二腭烷、三腭烷、四噚烷、氧化環己烯、氧化苯乙烯、 表氯醇、縮水甘油醚、烯丙基縮水甘油醚、碳酸烯丙酯縮 水甘油酯、單氧化丁二烯、單氧化異戊間二烯、乙烯基氧 雜環丁烷、乙烯基四氫呋喃、乙烯基氧化環己烯、苯基縮 水甘油醚、丁基縮水甘油醚、及苯甲酸縮水甘油酯。兩種 或多種離子可聚合環狀化合物之特例有四氫呋喃與氧化乙 烯、四氫呋喃與氧化丙烯、四氫呋喃與2 -曱基四氫呋喃 、四氫呋喃與3 -甲基四氫呋喃、氧化乙烯與氧化丙烯、 丁烯- 1 -氧化物與氧化乙烯、四氫呋喃、丁烯一 1 一氧 化物、及氧化乙烯之組合物、及其類者。 本紙張尺度適用中國國家標準(CNS ) A4規格(210Χ297公釐) 77 574339 A7 B7 五、發明説明(5 ) (請先閲讀背面之注意事項再填寫本頁) 藉此等離子可聚合環狀化合物及環狀亞胺諸如乙二亞 胺之開環共聚所製得之聚醚多元醇,亦可使用環內酯酸諸 如卢-丙內酯及乙醇酸交酯、或二甲基環聚矽氧烷。 脂環族聚醚多元醇之實例有氫化雙酚A之氧化烯加成 二元醇、氫化雙酚F之氧化烯加成二元醇、1 ,4 一環己 二醇之氧化烯加成二元醇及其類者。 芳族聚醚多元醇之實例有雙酚A之氧化烯加成二元醇 、雙酚F之氧化烯加成二元醇、氫醌之氧化烯加成二元醇 、萘氫醌之氧化烯加成二元醇、蒽氫醌之氧化烯加成二元 醇、及其類者。 脂族聚醚多元醇之實例有PTMG 650, PTMG 1000,PTMG 2000(Mitsubishi Chemical Corp.製造),PPG 1000,EXCENOL 1 020, EXCENOL 2020, EXCENOL 3020, EXCENOL 4020 (Asahi Glass Co·, Ltd.製造),PEG 1 000, 經濟部智慧財產局員工消費合作社印製The composition of the present invention preferably contains all four components (A)-(D). The present invention further proposes the use of the composition as an adhesive for an optical disc, such as a digital multi-purpose disk. Moreover, the present invention proposes an optical disc, such as a digital multi-purpose magnetic disc, which includes an adhesive that can be prepared by curing the composition of the present invention. Detailed description of the invention Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs The oligomers as component (A) may be any suitable radiation curable oligomers, such as (meth) acrylate oligomers. The preferred component (A) is a urethane (meth) acrylate oligomer, which can be reacted by reacting a polyol compound, a polyisocyanate compound, and a (meth) acrylate compound containing a hydroxyl group. be made of. As for the polyol compound, polyether polyol, polyester polyol, polycarbonate polyol, polycaprolactone polyol, aliphatic hydrocarbon having two or more hydroxyl groups in the molecule, Cycloaliphatic hydrocarbons having one or more hydroxyl groups, unsaturated hydrocarbons having two or more hydroxyl groups in the molecule, and the like. These polyols can be used individually or in combination of two or more. -6- This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) 574339 A7 B7 V. Description of the invention (4) Examples of polyether polyols are aliphatic polyether polyols, alicyclic polyether polyols Alcohols, and aromatic polyether polyols. (Please read the notes on the back before filling this page) Examples of aliphatic polyether polyols are polyethylene glycol, polypropylene glycol, polybutylene glycol, polyhexanediol, polyheptanediol, polydecanediol, Isopentaerythritol, diisopentaerythritol, trimethylolpropane; polyhydric alcohols such as alkylene oxide addition polyols such as trimethylolpropane of ethylene oxide addition triol, propylene oxide addition triol Trimethylolpropane, trimethylolpropane of ethylene oxide / propylene oxide addition triol, isoprene tetraol of ethylene oxide addition tetraol, and diisoprene tetraol of ethylene oxide addition hexaol Polyether polyols prepared by ring-opening polymerization of two or more ion-polymerizable cyclic compounds; and the like. Examples of ionic polymerizable cyclic compounds printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs are cyclic ethers such as ethylene oxide, propylene oxide, butene-1 monoxide, isobutylene oxide, 3,3-bis (chlorofluorenyl) Oxetane, tetrahydrofuran, 2-methyltetrahydrofuran, dioxane, trioxane, tetraoxane, cyclohexene oxide, styrene oxide, epichlorohydrin, glycidyl ether, allyl glycidyl ether, Allyl carbonate glycidyl ester, butadiene monooxide, isoprene monooxide, vinyloxetane, vinyl tetrahydrofuran, vinyl cyclohexene oxide, phenyl glycidyl ether, butyl glycidyl Glyceryl ether and glycidyl benzoate. Specific examples of two or more ionic polymerizable cyclic compounds are tetrahydrofuran and ethylene oxide, tetrahydrofuran and propylene oxide, tetrahydrofuran and 2-methyltetrahydrofuran, tetrahydrofuran and 3-methyltetrahydrofuran, ethylene oxide and propylene oxide, butene-1- Compositions of oxides and ethylene oxide, tetrahydrofuran, butene-1 monoxide, and ethylene oxide, and the like. This paper size applies Chinese National Standard (CNS) A4 specification (210 × 297 mm) 77 574339 A7 B7 V. Description of the invention (5) (Please read the precautions on the back before filling this page) The cyclic compounds can be polymerized by this plasma Polyether polyols prepared by ring-opening copolymerization of cyclic imines such as ethylene diimide. Cyclolactone acids such as lu-propiolactone and glycolide, or dimethylcyclopolysiloxane . Examples of alicyclic polyether polyols are alkylene oxide addition diols of hydrogenated bisphenol A, alkylene oxide addition diols of hydrogenated bisphenol F, and alkylene oxide addition diols of 1,4-monocyclohexanediol. Alcohol and its class. Examples of aromatic polyether polyols are oxyalkylene addition diols of bisphenol A, oxyalkylene addition diols of bisphenol F, oxyalkylene addition diols of hydroquinone, and oxyalkylene naphthalene hydroquinones Addition diols, anthrahydroquinone alkylene oxide addition diols, and the like. Examples of the aliphatic polyether polyol are PTMG 650, PTMG 1000, PTMG 2000 (manufactured by Mitsubishi Chemical Corp.), PPG 1000, EXCENOL 1 020, EXCENOL 2020, EXCENOL 3020, EXCENOL 4020 (manufactured by Asahi Glass Co., Ltd.) , PEG 1 000, printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs

Unisafe DC 1 100,Unisafe DC 1 800,Unisafe DCB 1100, Unisafe DCB 1 800 (Nippon Oil and Fats Co.,Ltd.製造),PPTG 1000, PPTG 2000, PPTG 4000, PTG 400, PTG 650, PTG 2000, PTG 3000,PTGL 1 000,PTGL 2000 (Hodogaya Chemical Co., Ltd.製造),PPG 400, PBG 400, Z-3001-4, Z-300 1 -5, PBG 2000, PBG 2000B (Daiichi Kogyo Seiyaku Co·,Ltd·製造),TMP30, PNT4 Glycol, ED A P4,ED A P8 (Nippon Ny ukazai Co.,Ltd.製 造)及Quadrol (Asahi Denka Kogyo Κ·Κ·製造)。芳族聚醚多兀 醇之市售產物實例有 Uniol DA400,DA700,DA1000,DB400 (Nippon Oil and Fats Co.,Ltd.製造)及其類者。 -8- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 B7 五、發明説明(6 ) (請先閲讀背面之注意事項再填寫本頁) 聚酯多元醇係藉著多羥醇與多元酸進行反應而製得。 多羥醇之實例有乙二醇、聚乙二醇、丙二醇、聚丙二醇、 丁二醇、聚丁二醇、1,4 一丁二醇、1,5 -戊二醇、 1 ,6 —己二醇、1 ,7 —庚二醇、1 ,8 —辛二醇、新 戊二醇、1 ,4 —環己二醇、1 ,4 一環己烷二甲醇、1 ,2 —雙(羥基乙基)環己烷、2,2 —二乙基—1 ,3 —丙二醇、3 —甲基一 1 ,5 -戊二醇、1 ,9 —壬烷二 醇、2 -甲基—1 ,8 -辛二醇、甘油、三羥甲基丙烷、 三羥甲基丙烷之氧化乙烯加成產物、三羥甲基丙烷之氧化 丙烯加成產物、三羥甲基丙烷之氧化乙烯與氧化丙烯加成 產物、山梨糖醇、異戊四醇、二異戊四醇、氧化烯加成多 元醇、及其類者。多元酸之實例有苯二甲酸、異苯二甲酸 、對苯二甲酸、順丁烯二酸、反丁烯二酸、己二酸、癸二 酸、及其類者。市告聚酯多元醇之實例有Kurapol P1010, Kurapol P2010, PMIPA, PKA-A, PKA-A2, PNA-2000 (Kuraray Co.,Ltd·製造)及其類者。 經濟部智慧財產局員工消費合作社印製 聚碳酸酯多元醇之實例有具有下式(1 )所示之聚碳 酸酯二醇: 0 ,II , HO—(R^O-C-O)—R^OH (1) 其中R1係表示具有2至2 0個碳原子之伸烷基、(聚)乙 二醇殘基、(聚)丙二醇殘基、或(聚)丁二醇殘基,且 m係爲由1至30之整數。 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) _ q 一 574339 A7 B7 五、發明説明(7 ) R 1所示之基團的特例有 自1 , 4 —— 丁 二醇、 1 5 - 戊 一 醇 、新戊 二醇 1, 6 -己 二 醇 1 5 4 - rm 場 己 院二 甲 醇 Λ 1,7 一庚 二 醇、 1 ,8 — 辛 二 醇 Λ 1, 9 — 壬二 醇 Λ 乙 二醇、 二( 乙 二醇 ) 、三 ( 乙 二 醇 ) 、四 ( 乙 二醇 ) Λ 丙 二醇、 二( 丙 二醇 ) 、 三 ( 丙 二 醇 ) 、四 ( 丙 二醇 ) 及 其 類者之 兩末 朗 去除 羥; 基所: 得 之 殘 基 Ο 聚碳 酸 酯 多元 醇 之 市 售產物的實例有 DN -980 Λ DN-981 Λ DN- 982、 DN- 9 83(Nippon Polyurethane Industry Co·,Ltd.製造)、PC-8000 (PPG 製造)、PN〇C 1000、PN〇C 2000、PMC 100、PMC 2000 (Kuraray Co., Ltd·製造)、PLACCEL CD-205, CD-208, CD-210, CD-220, CD-205PL,CD-208PL,CD-210PL,CD-220PL, CD-205HL,CD-208HL, CD-210HL, CD-220HL, CD-210T, CD-221T (Daicel Chemical Industries, Ltd.製造)及其類者。 (請先閲讀背面之注意事項再填寫本頁)Unisafe DC 1 100, Unisafe DC 1 800, Unisafe DCB 1100, Unisafe DCB 1 800 (manufactured by Nippon Oil and Fats Co., Ltd.), PPTG 1000, PPTG 2000, PPTG 4000, PTG 400, PTG 650, PTG 2000, PTG 3000, PTGL 1 000, PTGL 2000 (manufactured by Hodogaya Chemical Co., Ltd.), PPG 400, PBG 400, Z-3001-4, Z-300 1 -5, PBG 2000, PBG 2000B (Daiichi Kogyo Seiyaku Co. ,, Ltd.), TMP30, PNT4 Glycol, ED A P4, ED A P8 (manufactured by Nippon Ny ukazai Co., Ltd.) and Quadrol (manufactured by Asahi Denka Kogyo KK). Examples of commercially available products of aromatic polyether polyols include Uniol DA400, DA700, DA1000, DB400 (manufactured by Nippon Oil and Fats Co., Ltd.) and the like. -8- This paper size applies to Chinese National Standard (CNS) A4 (210X297 mm) 574339 A7 B7 V. Invention Description (6) (Please read the notes on the back before filling this page) Polyester polyols Polyol is prepared by reacting a polyhydric alcohol with a polybasic acid. Examples of polyhydric alcohols are ethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol, butylene glycol, polybutylene glycol, 1,4-monobutylene glycol, 1,5-pentanediol, 1,6-hexane Diol, 1,7-heptanediol, 1,8-octanediol, neopentyl glycol, 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, 1,2-bis (hydroxyethyl Group) cyclohexane, 2,2-diethyl-1,3-propanediol, 3-methyl-1,5-pentanediol, 1,9-nonanediol, 2-methyl-1,8 -Octanediol, glycerol, trimethylolpropane, ethylene oxide addition product of trimethylolpropane, propylene oxide addition product of trimethylolpropane, ethylene oxide and propylene oxide addition of trimethylolpropane Products, sorbitol, isopentaerythritol, diisopentaerythritol, alkylene oxide addition polyols, and the like. Examples of the polybasic acid are phthalic acid, isophthalic acid, terephthalic acid, maleic acid, fumaric acid, adipic acid, sebacic acid, and the like. Examples of commercially available polyester polyols include Kurapol P1010, Kurapol P2010, PMIPA, PKA-A, PKA-A2, PNA-2000 (manufactured by Kuraray Co., Ltd.) and the like. Examples of polycarbonate polyols printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs are polycarbonate diols having the following formula (1): 0, II, HO— (R ^ OCO) —R ^ OH (1 ) Wherein R1 represents an alkylene group having 2 to 20 carbon atoms, a (poly) ethylene glycol residue, a (poly) propylene glycol residue, or a (poly) butanediol residue, and m is represented by 1 An integer up to 30. This paper size applies the Chinese National Standard (CNS) A4 specification (210 X 297 mm) _ q 574339 A7 B7 V. Description of the invention (7) Specific examples of the groups shown in R 1 are from 1, 4-Ding Er Alcohol, 1 5-pentyl alcohol, neopentyl glycol 1, 6-hexanediol 1 5 4-rm changjiyuan dimethanol Λ 1,7 heptanediol, 1, 8 — octanediol Λ 1, 9 — Nonanediol Λ ethylene glycol, di (ethylene glycol), tri (ethylene glycol), tetra (ethylene glycol) Λ propylene glycol, di (propylene glycol), tri (propylene glycol), tetra (propylene glycol) and the like Examples of commercially available products of polycarbonate polyols are DN-980 Λ DN-981 Λ DN- 982 and DN-9 83 (Nippon Polyurethane Industry Co., Ltd.), PC-8000 (manufactured by PPG), PNOC 1000, PNOC 2000, PMC 100, PMC 2000 (manufactured by Kuraray Co., Ltd.), PLACCEL CD-205, CD-208, CD-210 , CD-220, CD-205PL, CD-208PL, CD-210PL, CD-220PL, CD-205HL, CD-208HL, CD-210HL, CD-220HL, CD-210T, CD-221T (Daicel Che mical Industries, Ltd.) and others. (Please read the notes on the back before filling this page)

、1T --. 經濟部智慧財產局員工消費合作社印製 聚己內酯多元醇之實例有藉ε -己內酯及多元醇諸如 乙二醇、聚乙二醇、丙二醇、聚丙二醇、丁二醇、聚丁二 醇、1 ,2 —聚丁二醇、1 ,6 -己二醇、新戊二醇、1 ’ 4 —環己烷二甲醇、或1 ,4 一丁二醇之加成反應所製 得之聚己內酯二醇。此等聚己內酯二醇之市售產物的實例 有 PLACCEL 205、205 AL、212、212 AAL、220、 220AL(Daicel Chemical Industries,Ltd.製造)及其類者。 分子中具有兩個或多個羥基之脂族烴的實例有乙二醇 、丙二醇、丁二醇、1,4一 丁二醇、1 ,5 —戊二醇、 1 ,6 —己二醇、1 ,7 —庚二醇、1 ,8- 辛二醇、1 ,9 —壬二醇、新戊二醇、2,2 —二乙基一 1 ,3 -丙 -10- 本紙張尺度適用中國國家標準(CNS ) A4規格(210'〆297公釐) 574339 A7 ____ B7 五、發明説明(8 ) 二醇、3 —甲基—1 ,5 -戊二醇、2 —甲基—1 ,8-辛二醇、具有末端羥基之氫化聚丁二烯、甘油、三羥甲基 丙烷、異戊四醇、山梨糖醇及其類者。 分子中具有兩個或多個羥基之脂環族烴之實例有1, 4 一環己二醇、1 ,4 —環己二甲醇、1 ,2 —雙(羥乙 基)環己烷、二羥甲基化合物或環戊二烯、三環癸烷二甲 醇及其類者。 分子中具有兩個或多個羥基之不飽和烴的實例有具有 末端羥基之聚丁二烯、具有末端羥基之聚異戊間二烯、及 其類者。 除前述多元醇以外之多元醇實例有ys -甲基- 5 -戊 內酯二醇、經篦麻油修飾之二醇、聚二甲基矽氧烷之末端 二醇化合物、經聚二曱基矽氧烷卡必醇修飾之二醇、及其 類者。 此等多元醇藉凝膠滲透層析(G P C )測定之經聚苯 乙烯降低的數量平均分子量以50 - 15,000爲佳, 尤其是250 — 800。 就聚異氰酸酯而言,以二異氰酸酯化合物爲佳。二異 氰酸酯化合物之實例有2,4 一二甲苯二異氰酸酯、2, 6 一二甲苯二異氰酸酯、1 ,3 —二甲苯二異氰酸酯、1 ,4 一二甲苯二異氰酸酯、1 ,5 —萘二異氰酸酯、間一 苯二異氰酸酯、對一苯二異氰酸酯、3 ,3’ 一二甲基一 4,4’ 一二苯基甲烷二異氰酸酯、4,4’ —二苯基甲 烷二異氰酸酯、3 ,3’ 一二甲基苯二異氰酸酯、4 ’ 4 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -11 - (請先閲讀背面之注意事項再填寫本頁) ^裝· 經濟部智慧財產局員工消費合作社印製 574339 Α7 Β7 五、發明説明(9 ) 〜聯苯二異氰酸酯、1 ,6 一己烷二異氰酸酯、異佛爾 (請先閲讀背面之注意事項再填寫本頁) 嗣二異氰酸酯、2,2,4 一三甲基伸己基二異氰酸酯、 雙(2 -異氰酸基乙基)反丁烯二酸酯、6 -異丙基一 1 ’ 3 -苯基二異氰酸酯、4 一二苯基丙烷二異氰酸酯、離 月安酸二異氰酸酯、氫化二苯基甲烷二異氰酸酯、氫化二甲 苯二異氰酸酯、四甲基二甲苯二異氰酸酯、及其類者。其 中’ 2,4一二甲苯二異氰酸酯、2 ,6 —二甲苯二異氰 酸酯、氫化二曱苯二異氰酸酯、異佛爾酮二異氰酸酯、氫 化二苯基甲烷二異氰酸酯及其類者特佳。此等二異氰酸酯 可個別或兩種或多種組合使用。 經濟部智慧財產局員工消費合作社印製 含有羥基之(甲基)丙烯酸酯在酯殘基中具有羥基。 例如(甲基)丙烯酸2 -羥基乙酯、(甲基)丙烯酸2 -羥基丙酯、(甲基)丙烯酸4一羥基丁酯、(甲基)丙烯 酸2 -羥基一 3 —苯氧丙酯、1 ,4 一丁二醇單(甲基) 丙烯酸酯、(甲基)丙烯醯磷酸2 -羥基烷酯、(甲基) 丙烯酸4-徑基環己酯、1 ’ 6 —己二醇單(甲基)丙烯 酸酯、新戊二醇單(甲基)丙烯酸酯、三羥甲基丙院二( 甲基)丙烯酸酯、三羥甲基乙烷二(甲基)丙燦酸酯、異 戊四醇三(甲基)丙烯酸酯、二異戊四醇五(甲基)丙燦 酸酯、具有下式(2 )之(甲基)丙烯酸酯及其類者: CH2=〒一 g-〇CH2CH广(Oj^CH2CH2CH2CH2CH2>n-〇H (2) R2 0 0 其中R2係表示氫原子或甲基,且η係爲由1至1 5之整數 -12- 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) 574339 A7 B7 五、發明説明(10) (請先閲讀背面之注意事項再填寫本頁) ,以1至4爲佳。此外,亦可使用藉著含有縮水甘油基之 化合物諸如烷基縮水甘油基醚、烯丙基縮水甘油基醚、或 (甲基)丙烯酸縮水甘油酯、及(甲基)丙烯酸之加成反 應所得的化合物。其中以(甲基)丙烯酸羥基烷酯諸如( 甲基)丙烯酸2 —羥基乙酯、(甲基)丙烯酸2 -羥基丙 酯、及(甲基)丙烯酸4 -羥基丁酯特佳。 合成該胺基甲酸酯(曱基)丙烯酸酯之方法並無特別 限制。例如,可採用以下方法(i )至(i i i )。 (i) 多異氰酸酯與含有羥基之(甲基)丙烯酸酯進行反應 ,形成之產物與該多元醇進行反應的方法。 (ii) 該多元醇、多異氰酸酯、及含有羥基之(甲基)丙儲 酸酯皆一起進行反應之方法。 (iii) 該多元醇與多異氰酸酯進行反應,且形成之產物與含 有羥基之(甲基)丙烯酸酯進行反應之方法。 經濟部智慧財產局員工消費合作社印製 較佳係使用每1 〇 〇重量份數反應產物爲 0 . 0 1 P e 1重量份數之量的尿烷化觸媒諸如環烷酸 銅、環烷酸鈷、環烷酸鋅、二月桂酸二正丁基錫、三乙胺 1 ’ 4 —* 氮雑 一^環〔2 · 2 · 2〕辛院、或 1 ,4 一 二氮雜一 2 -甲基二環〔2 _ 2 . 2〕辛烷合成本發明所 使用之胺基甲酸酯(甲基)丙烯酸酯。該反應通常係於由 0至9 0 °C之溫度下進行,以由1 〇至8 〇。〇爲佳。 本發明所使用之胺基甲酸酯(甲基)丙烯酸酯的數量 平均分子量以400 — 20,000爲佳,7 0 0 — 5,0 0 0特佳。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -13- 574339 A7 B7 五、發明説明(11) (請先閲讀背面之注意事項再填寫本頁) 就對於基材之膠黏性及組合物之黏度而言,本發明組 合物中胺基甲酸酯(甲基)丙烯酸酯相對於組合物總重之 比例較佳係2 0至8 0重量百分比。 本發明所使用之組份(B )的實例係包括二烷基胺基 苯甲酸之烷酯(甲酯、乙酯、丙酯、丁酯、異戊酯等)( 二烷基胺基苯甲酸烷酯)。供二烷基胺基使用之較佳烷基 包括具有1至6個碳原子之烷基。就酯殘基而言,以具有 1至6個碳原子之烷基爲佳。該二烷基胺基及羧酸酯較佳 係鍵結於苯環之對位。當置於兩磁碟間之組合物固化時, 該組份(B )防止膠黏,且改善磁碟邊緣之固化性。其中 ,以對-二曱基胺基苯甲酸乙酯爲佳。 作爲組份(B )之市售產物的實例有KAYACURE EPA, KAYACURE DMBI (Nippon Kayaku Co.,Ltd.製造)〇 就邊緣固化性及耐濕熱性而言,本發明組合物中組份 (B )相對於組合物總重之比例以〇 . 〇 5 - 5重量百分 比爲佳,0 · 1至3重量百分比更佳,〇 · 2 - 1重量百 分比特佳。 經濟部智慧財產局員工消費合作社印製 使用於本發明之組份(C )實例係包括(甲基)丙烯 酸C 1 一 C 6烷酯,例如(甲基)丙烯酸2 —羥基乙酯、 (甲基)丙烯酸2 -羥基丙酯、及(甲基)丙烯酸4 -羥 基丁酯。組份(C )改善耐濕熱性。其中,以(甲基)丙 烯酸4 -羥基丁酯爲佳。 作爲組份(C )之市售產物實例有HEA、ΗΡΑ、4HBA (Osaka Organic Chemical Industry Co.,Ltd.製造)、輕酯 Η〇Α -14- 本紙張尺度適用中國國家標隼(CNS ) Α4規格(210X 297公釐) 574339 A7 B7 五、發明説明(12 ) 、輕酯HOP-A、輕酯H〇、輕酯HOP、輕酯H〇B (Kyoeosha Chemical c〇·,Ltd.製造)及其類者。 (請先閱讀背面之注意事項再填寫本頁) 作爲組份(C )之(甲基)丙烯酸羥烷酯相對於該組 合物之總重的比例以5 - 7 0重量百分比爲佳,1 〇 一 5 0重量百分比更佳,以改善耐濕熱性。 組份(D )--感光起始劑一一係爲至少一種選自包 括2,2 -二甲氧基—1 ,2 —二苯基乙—i —酮、2 — 羥基一 2 -甲基一 1 一苯基丙一 1 一酮、及1 一羥基環己 基苯基酮之群的化合物。較佳係使用2,2 -二甲氧基-1 ’ 2 -二苯基乙—1_酮及2 —羥基-2 -甲基—1 — 苯基丙- 1 -酮之組合物。就而濕熱性及固化性而言,該 組份(D )於本發明組合物中相對於組合物總重之比例以 〇 . 01 - 1 5重量百分比爲佳,0 · 1 - 1〇重量百分 比更佳。 作爲組份(D )之市售產物實例有lrgacure 184、500、 651、Darocur 1173、4265 (Ciba Specialty Chemicals Co., Ltd.製造)及其類者。 經濟部智慧財產局員工消費合作社印製 較佳係添加含有甲氧基甲矽烷基之硫醇化合物於本發 明供光碟使用之膠黏性組合物中,以作爲組份(E ),而 改善對黃金之膠黏性。該含有甲氧基甲矽烷基之硫醇化合 物實例有氫硫基烷基單-、二-及三-甲氧基矽烷諸如r -氫硫基丙基三甲氧基矽烷、r -氫硫基丙基甲基單甲氧 基矽烷、及r -氫硫基丙基曱基二甲氧基矽烷。若使用組 份(E ),則就其對於黃金之膠黏性及耐濕熱性而言’在 -15- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 B7 五、發明説明(13) 本發明組合物中之比例相對於該組合物之總重較佳係爲 0 · 1 - 5重量百分比,0 · 3 - 3重量百分比更佳。 (請先閲讀背面之注意事項再填寫本頁) 可作爲組份(E )之市售產物實例包括SH 6 0 6 2 'AY43-062 ( Toray-Dow Corning Silicone Co., Ltd. 製造)、Sila-Ace S810 (Chisso Corp.製造)及〖314803 (31^11-, 1T-. Examples of polycaprolactone polyols printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs include ε-caprolactone and polyols such as ethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol, butane Addition of alcohol, polybutanediol, 1,2-polybutanediol, 1,6-hexanediol, neopentyl glycol, 1'4-cyclohexanedimethanol, or 1,4-monobutylene glycol Polycaprolactone diol prepared by the reaction. Examples of such commercially available products of polycaprolactone diol are PLACCEL 205, 205 AL, 212, 212 AAL, 220, 220AL (manufactured by Daicel Chemical Industries, Ltd.) and the like. Examples of aliphatic hydrocarbons having two or more hydroxyl groups in the molecule are ethylene glycol, propylene glycol, butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, neopentyl glycol, 2,2-diethyl-1,3-propane-10- This paper size applies to China National Standard (CNS) A4 specification (210'〆297 mm) 574339 A7 ____ B7 V. Description of the invention (8) Glycol, 3-methyl-1, 5-pentanediol, 2-methyl-1, 8 -Octanediol, hydrogenated polybutadiene with terminal hydroxyl groups, glycerol, trimethylolpropane, isoprene tetraol, sorbitol and the like. Examples of alicyclic hydrocarbons having two or more hydroxyl groups in the molecule are 1, 4-monocyclohexanediol, 1, 4-cyclohexanedimethanol, 1, 2-bis (hydroxyethyl) cyclohexane, dihydroxy Methyl compounds or cyclopentadiene, tricyclodecanedimethanol and the like. Examples of unsaturated hydrocarbons having two or more hydroxyl groups in the molecule are polybutadiene having terminal hydroxyl groups, polyisoprene having terminal hydroxyl groups, and the like. Examples of polyols other than the aforementioned polyols are ys-methyl-5 -valerolactone diol, diols modified with ramie oil, terminal diol compounds of polydimethylsiloxane, and polydifluorinated silicon Oxalcarbitol-modified diols and the like. These polyols have a reduced average molecular weight of polystyrene by gel permeation chromatography (GPC) of 50 to 15,000, especially 250 to 800. As the polyisocyanate, a diisocyanate compound is preferred. Examples of diisocyanate compounds are 2,4-xylene diisocyanate, 2,6-xylene diisocyanate, 1,3-xylene diisocyanate, 1,4-xylene diisocyanate, 1,5-naphthalene diisocyanate, M-phenylenediisocyanate, p-phenylenediisocyanate, 3,3'-dimethyl-4,4'-diphenylmethane diisocyanate, 4,4'-diphenylmethane diisocyanate, 3,3'- Dimethylbenzene diisocyanate, 4 '4 This paper size is applicable to Chinese National Standard (CNS) A4 specification (210X297 mm) -11-(Please read the precautions on the back before filling this page) Printed by the Bureau ’s Consumer Cooperatives 574339 Α7 B7 V. Description of the Invention (9) ~ Biphenyl diisocyanate, 1, 6-hexane diisocyanate, isophor (please read the precautions on the back before filling this page) 嗣 diisocyanate, 2,2,4 monotrimethylhexyl diisocyanate, bis (2-isocyanatoethyl) fumarate, 6-isopropyl-1 '3-phenyldiisocyanate, 4 one two Phenylpropane diisocyanate An month from acid diisocyanate, hydrogenated diphenylmethane diisocyanate, hydrogenated xylene diisocyanate, tetramethyl xylene diisocyanate, and those classes. Of these, '2,4-xylene diisocyanate, 2,6-xylene diisocyanate, hydrogenated diphenylbenzene diisocyanate, isophorone diisocyanate, hydrogenated diphenylmethane diisocyanate and the like are particularly preferred. These diisocyanates can be used individually or in combination of two or more. Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs. (Meth) acrylates containing hydroxyl groups have hydroxyl groups in the ester residues. For example, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 2-hydroxy-3 -phenoxypropyl (meth) acrylate, 1,4 monobutanediol mono (meth) acrylate, (meth) acrylic acid 2-hydroxyalkyl phosphate, 4-methylcyclohexyl (meth) acrylate, 1 '6-hexanediol mono ( (Meth) acrylate, neopentyl glycol mono (meth) acrylate, trimethylolpropane di (meth) acrylate, trimethylolethane di (meth) propionate, isoamyl Tetraol tri (meth) acrylate, diisopentaerythritol penta (meth) propionate, (meth) acrylates having the following formula (2) and the like: CH2 = 〒1-g-〇 CH2CH 广 (Oj ^ CH2CH2CH2CH2CH2 > n-〇H (2) R2 0 0 where R2 is a hydrogen atom or a methyl group, and η is an integer from 1 to 15-12- This paper applies the Chinese National Standard (CNS) ) A4 specification (210 × 297 mm) 574339 A7 B7 V. Description of the invention (10) (Please read the notes on the back before filling this page), preferably 1 to 4. In addition, you can also use A compound obtained by addition reaction of a glycidyl-containing compound such as an alkyl glycidyl ether, an allyl glycidyl ether, or glycidyl (meth) acrylate, and (meth) acrylic acid. Hydroxyalkyl (meth) acrylates such as 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and 4-hydroxybutyl (meth) acrylate are particularly preferred. The method of formate (fluorenyl) acrylate is not particularly limited. For example, the following methods (i) to (iii) can be used. (I) A polyisocyanate is reacted with a (meth) acrylate containing a hydroxyl group to form A method of reacting a product with the polyol. (Ii) A method of reacting the polyol, a polyisocyanate, and a (meth) propionate containing a hydroxyl group together. (Iii) A reaction of the polyol with a polyisocyanate. And the formed product is reacted with (meth) acrylic acid ester containing hydroxyl group. It is better to print the product by using the consumer cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs, which uses 1,000 parts by weight. The product is urethane catalysts such as copper naphthenate, cobalt naphthenate, zinc naphthenate, di-n-butyltin dilaurate, triethylamine 1 '4-1 parts by weight. * Aza-Cyclo [2 · 2 · 2] Xin Yuan, or 1, 4-Diaza- 2-methylbicyclo [2-2. 2] octane to synthesize the amino formic acid used in the present invention Ester (meth) acrylate. The reaction is usually carried out at a temperature from 0 to 90 ° C, preferably from 10 to 80.0. The urethane (methyl) used in the present invention ) The number average molecular weight of acrylate is preferably from 400 to 20,000, and particularly preferably from 700 to 5,000. This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) -13- 574339 A7 B7 V. Description of the invention (11) (Please read the precautions on the back before filling this page) In terms of properties and viscosity of the composition, the ratio of the urethane (meth) acrylate to the total weight of the composition in the composition of the present invention is preferably 20 to 80 weight percent. Examples of the component (B) used in the present invention include alkyl esters (methyl, ethyl, propyl, butyl, isoamyl, etc.) of dialkylaminobenzoic acid (dialkylaminobenzoic acid) Alkyl ester). Preferred alkyl groups for use with dialkylamino groups include alkyl groups having 1 to 6 carbon atoms. As the ester residue, an alkyl group having 1 to 6 carbon atoms is preferred. The dialkylamino group and the carboxylic acid ester are preferably bonded to the para position of the benzene ring. When the composition placed between two magnetic disks is cured, the component (B) prevents sticking and improves the curability of the disk edge. Among them, ethyl p-difluorenylaminobenzoate is preferred. Examples of commercially available products as component (B) are KAYACURE EPA, KAYACURE DMBI (manufactured by Nippon Kayaku Co., Ltd.). In terms of edge curability and moisture and heat resistance, component (B) in the composition of the present invention The ratio to the total weight of the composition is preferably from 0.05 to 5 weight percent, more preferably from 0.1 to 3 weight percent, and particularly from 0.2 to 1 weight percent. Examples of the component (C) printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs for use in the present invention include C 1 -C 6 alkyl (meth) acrylates, such as 2-hydroxyethyl (meth) acrylate, (formaldehyde) 2-hydroxypropyl acrylate and 4-hydroxybutyl (meth) acrylate. Component (C) improves damp heat resistance. Among them, 4-hydroxybutyl (meth) acrylate is preferred. Examples of commercially available products as the component (C) are HEA, HPA, 4HBA (manufactured by Osaka Organic Chemical Industry Co., Ltd.), light esters 〇Α -14- This paper applies Chinese National Standard (CNS) Α4 Specifications (210X 297 mm) 574339 A7 B7 5. Description of the invention (12), light ester HOP-A, light ester H0, light ester HOP, light ester HOB (manufactured by Kyoeosha Chemical Co., Ltd.) and Its kind. (Please read the precautions on the back before filling this page) As the component (C), the ratio of the hydroxyalkyl (meth) acrylate to the total weight of the composition is preferably 5-70 weight percent, 1 〇 A 50 weight percent is better to improve moisture and heat resistance. Component (D)-the photoinitiator is at least one selected from the group consisting of 2,2-dimethoxy-1, 2-diphenylethyl-i-one, and 2-hydroxy-2-methyl Compounds of 1 1 phenylpropanyl 1 ketone, and 1 hydroxycyclohexyl phenyl ketone. It is preferred to use a combination of 2,2-dimethoxy-1 '2-diphenylethyl-1-one and 2-hydroxy-2-methyl-1-phenylpropan-1-one. In terms of moist heat and curing properties, the proportion of the component (D) in the composition of the present invention with respect to the total weight of the composition is preferably 0.01 to 15 weight percent, and 0.1 to 10 weight percent. Better. Examples of commercially available products as component (D) include lrgacure 184, 500, 651, Darocur 1173, 4265 (manufactured by Ciba Specialty Chemicals Co., Ltd.) and the like. The printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs is better to add a thiol compound containing a methoxysilyl group to the adhesive composition for optical discs of the present invention as a component (E) to improve the The stickiness of gold. Examples of the methoxysilyl-containing thiol compound are hydrothioalkyl mono-, di-, and tri-methoxysilanes such as r-hydrothiopropyltrimethoxysilane, r-hydrothiopropyl Methylmethylmonomethoxysilane and r-hydrothiopropylfluorenyldimethoxysilane. If component (E) is used, in terms of its adhesion to gold and moisture and heat resistance, it is -15- This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) 574339 A7 B7 V. Explanation of the invention (13) The proportion in the composition of the present invention with respect to the total weight of the composition is preferably from 0. 1-5 weight percent, and more preferably from 0. 3 to 3 weight percent. (Please read the notes on the back before filling this page) Examples of commercially available products that can be used as component (E) include SH 6 0 6 2 'AY43-062 (manufactured by Toray-Dow Corning Silicone Co., Ltd.), Sila -Ace S810 (made by Chisso Corp.) and 314803 (31 ^ 11-

Etsu Chemical Co.,Ltd.製造)。 除組份(C )以外而分子中含有至少一個(曱基)丙 烯醯基之(甲基)丙烯酸酯化合物可添加於本發明組合物 中。含有一個(甲基)丙烯醯基之單官能基化合物及含有 兩個或多個(甲基)丙烯醯基之多官能基化合物中之任何 一種皆可使用。此等化合物可於適當之比例下使用。 經濟部智慧財產局員工消費合作社印製 前述單官能基化合物之實例係包括(甲基)丙嫌酸甲 酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基 )丙烯酸異丙酯、(甲基)丙烯酸丁酯、(甲基)丙烯酸 戊酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第三丁酯 、(甲基)丙烯酸戊酯、(甲基)丙烯酸異戊酯、(甲基 )丙烯酸己酯、(甲基)丙烯酸庚酯、(甲基)丙烯酸辛 酯、(曱基)丙烯酸異辛酯、(甲基)丙烯酸2—乙基己 酯、(甲基)丙烯酸壬酯、(曱基)丙烯酸癸酯、(甲基 )丙烯酸異癸酯、(甲基)丙烯酸十一碳酯、(甲基)丙 烯酸十二碳酯、(甲基)丙烯酸月桂酯、(甲基)丙嫌酸 十八碳酯、(甲基)丙烯酸硬脂酯、(甲基)丙嫌酸四氫 糠酯、(甲基)丙烯酸丁氧乙酯、(甲基)丙燦酸乙氧基 一乙一醇酯、(甲基)丙烯酸;酯、(甲基)丙燒酸環己 -16- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(14) 胃曰、(甲基)丙烯酸苯氧乙酯、聚乙二醇單(甲基)丙烯 酸酉旨、聚丙二醇單(甲基)丙烯酸酯、甲氧基乙二醇單( 甲基)丙烯酸酯、(甲基)丙烯酸乙氧乙酯、(甲基)丙 矯酸乙氧基乙氧乙酯、曱氧基聚乙二醇(甲基)丙烯酸酯 、.甲氧丙基丙二醇(甲基)丙烯酸酯、(甲基)丙烯酸二 環戊二烯酯、(甲基)丙烯酸二環戊酯、(甲基)丙烯酸 二環戊烯酯、(甲基)丙烯酸三環癸酯、(甲基)丙烯酸 宿酯、(甲基)丙烯酸異萡酯、(甲基)丙烯酸金剛酯、 (甲基)丙烯酸二甲基胺基乙酯、(甲基)丙烯酸二乙基 胺基乙酯、(甲基)丙烯酸7-胺基一3,7—二甲基辛 酯、(甲基)丙烯醯嗎啉、2 —(甲基)丙烯醯氧乙基苯 二甲酸、2 — (甲基)丙烯醯氧乙基六氫苯二甲酸、2 -(甲基)丙烯醯氧丙基苯二甲酸、2 —(甲基)丙烯醯氧 丙基四氫苯二甲酸、2 -(甲基)丙醯氧丙基六氫苯二 甲酸、2—(甲基)丙烯醯氧乙基丁二酸、(甲基)丙烯 酸三氟乙酯、(甲基)丙烯酸四氫丙酯、(甲基)丙燃酸 六氟丙酯、(甲基)丙烯酸八氟戊酯、(甲基)丙烯酸十 七氟癸酯、單〔2 -(甲基)丙烯醯氧乙基〕磷酸酯、單 〔2 -(甲基)丙烯醯氧乙基〕二苯基磷酸酯、單〔2 — (甲基)丙烯醯氧丙基〕磷酸酯、及下式(3 )至(5) 所示之化合物: CH^C—C-0—(R3〇)p~⑶ R4 〇 (請先閱讀背面之注意事項再填寫本頁) ;衣· 訂 d 本紙張尺度適用中國國家標準(CNS ) A4規格(21 OX 297公釐) 574339 A7 B7 五、發明説明(15 ) 其中R3係表示具有2 - 6個碳原子之伸烷基或羥基伸烷基 ’ R4係表示氫原子或甲基,R5係表示氫原子或具有1至 1 2個碳原子之院基,且p係爲由〇至2 0之整數;Etsu Chemical Co., Ltd.). In addition to component (C), a (meth) acrylate compound containing at least one (fluorenyl) acrylfluorenyl group in the molecule may be added to the composition of the present invention. Any one of a monofunctional compound containing one (meth) acrylfluorenyl group and a polyfunctional compound containing two or more (meth) acrylfluorenyl groups can be used. These compounds can be used in an appropriate ratio. Examples of the printing of the aforementioned monofunctional compounds by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs include methyl (meth) propanoate, ethyl (meth) acrylate, propyl (meth) acrylate, (meth) acrylic Isopropyl ester, butyl (meth) acrylate, amyl (meth) acrylate, isobutyl (meth) acrylate, third butyl (meth) acrylate, amyl (meth) acrylate, (meth) ) Isoamyl acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, isooctyl (fluorenyl) acrylate, 2-ethylhexyl (meth) acrylate , Nonyl (meth) acrylate, decyl (fluorenyl) acrylate, isodecyl (meth) acrylate, undecyl (meth) acrylate, dodecyl (meth) acrylate, (meth) Lauryl acrylate, stearyl (meth) propionic acid, stearyl (meth) acrylate, tetrahydrofurfuryl (meth) propionic acid, butoxyethyl (meth) acrylate, (methyl) ) Propanoic acid ethoxy monoethylene glycol ester, (meth) acrylic acid; ester, Methyl) cyclohexyl-16- This paper size is in accordance with Chinese National Standard (CNS) A4 (210X297 mm) 574339 A7 B7 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 5. Description of the invention (14) Stomach said , Phenoxyethyl (meth) acrylate, polyethylene glycol mono (meth) acrylate, polypropylene glycol mono (meth) acrylate, methoxyethylene glycol mono (meth) acrylate, (formaldehyde) Base) ethoxyethyl acrylate, ethoxyethoxyethyl (meth) propanoate, ethoxy polyethylene glycol (meth) acrylate, methoxypropyl propylene glycol (meth) acrylate, Dicyclopentadienyl (meth) acrylate, dicyclopentyl (meth) acrylate, dicyclopentenyl (meth) acrylate, tricyclodecyl (meth) acrylate, ethyl (meth) acrylate , Isoamyl (meth) acrylate, adamantyl (meth) acrylate, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, (meth) acrylate 7 -Amino- 3,7-dimethyloctyl ester, (meth) acrylic morpholine, 2 — ( ) Acrylic acid oxyethyl phthalic acid, 2- (meth) acrylic acid oxyethyl hexahydrophthalic acid, 2- (meth) acrylic acid oxypropyl phthalic acid, 2- (meth) acrylic acid Hydroxypropyltetrahydrophthalic acid, 2- (meth) propoxypropylhexahydrophthalic acid, 2- (meth) acrylic acid, oxyethylsuccinic acid, trifluoroethyl (meth) acrylate Ester, tetrahydropropyl (meth) acrylate, hexafluoropropyl (meth) propionate, octafluoropentyl (meth) acrylate, heptafluorodecyl (meth) acrylate, mono [2-( (Meth) acryloxyethyl] phosphate, mono [2- (meth) acryloxyethyl] diphenyl phosphate, mono [2- (meth) acryloxypropyl] phosphate, and Compounds represented by the following formulas (3) to (5): CH ^ C—C-0— (R3〇) p ~ ⑶ R4 〇 (Please read the precautions on the back before filling out this page); Paper size applies Chinese National Standard (CNS) A4 specification (21 OX 297 mm) 574339 A7 B7 V. Description of the invention (15) where R3 represents an alkylene or hydroxyalkylene having 2 to 6 carbon atoms' R4 Department representation A hydrogen atom or a methyl group, R5 represents a hydrogen atom or a radical having 1 to 12 carbon atoms, and p is an integer from 0 to 20;

Ch^?~m~(orV~〇CH2Ch ^? ~ M ~ (orV ~ 〇CH2

(4) 其中R6係表示氫原子或甲基,R7係表示具有2 — 8個碳 原子之伸烷基,且q係爲由0至8之整數;(4) wherein R6 represents a hydrogen atom or a methyl group, R7 represents an alkylene group having 2 to 8 carbon atoms, and q is an integer from 0 to 8;

CHCH

CH3 〇. fC—C—(〇R9C)[—〇CH2—〒——CH r~CH3 〇. FC—C— (〇R9C) [— 〇CH2—〒——CH r ~

L II IJ o o CH, 0- (請先閱讀背面之注意事項再填寫本頁)L II IJ o o CH, 0- (Please read the notes on the back before filling this page)

CC

Rio R11 (5) 其中R8係表示氫原子或甲基,R9係表示具有2 — 8個碳 原子之伸烷基,r係爲由0至8之整數,且R1Q及R11係 表示氫原子或具有1 - 6個碳原子之烷基。 經濟部智慧財產局員工消費合作社印製 此等單官能基化合物之市售產物實例係包括Aronix M101,M102,M110,M113,M114,M117,M120,M152,M154, M5300,M5400,M5500, M5600 (Toagosei Co·,Ltd.製造), KAYARAD TC-110S, R128H, R629, R644 (Nippon Kayaku Co., Ltd 製造),IPAA,AIB,SBAA,TBA,IAAA,HEXA,CHA, N〇AA, I〇AA, INAA, LA, TDA, MSAA, CAA, HDAA, LTA, STA,ISAA-1, 〇DAA,NDAA, IBXA,ADAA,TCDA,2-MTA, DMA,Viscoat #150,#150D,#155,#158,#160,#190,#190D, #192, #193, #220, #320, #2311HP, #2000, #2100, #2150, #2180, MTG (Osaka Organic Chemical Industry Co·,Ltd.製造 -18- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(16 ) ),NK Ester M-20G,M-40G,M-90G,M-230G,CB-1,SA,S, AMP-10G, AMP-20G, AMP-60G, AMP-90G, A-SA, NLA (Shin- Nakamura Chemical Co.,Ltd.製造),ACM〇(Kojin Co.,Ltd.製 造)、輕丙烯酸酯IA-A,L-A,S-A,B〇-A,EC-A,MTG-A,DPM-A, PO-A, P-2O0A, THF-A, IB-XA, HOA-MS, HOA-MPL, HOA-MPE, HOA-HH, IO-A, BZ-A, NP-EA, NP-10EA, HOB-A, FA-108、環氧酯 M-600A、輕酯 P-M (Kyoeisha Chemical Co·,Ltd· 製造)、FA-511,FA-512A,FA-513A (Hitachi Chemical Co., Ltd·製造),AR-100,MR-100,MR-200,MR-260 (Daihachi Chemical Co.,Ltd.製造),JAMP-100,JAMP-514,JPA-514 (Johoku Chemical Co.,Ltd·製造)及其類者。 前述多官能基化合物之實例係包括乙二醇二(甲基) 丙儲酸酯、丙二醇二(甲基)丙燒酸酯、1 ,4- 丁二醇 二(甲基)丙烯酸酯、1 ,6 —己二醇二(甲基)丙烯酸 酯、1 ,9 一壬二醇二(曱基)丙烯酸酯、二(乙二醇) 二(甲基)丙烯酸酯、三(乙二醇)二(甲基)丙烯酸酯 '四(乙二醇)二(甲基)丙烯酸酯、丙二醇二(甲基) 丙烯酸酯、二(丙二醇)二(甲基)丙烯酸酯、三(丙二 醇)二(甲基)丙烯酸酯、聚丙二醇二(甲基)丙烯酸酯 、新戊一醇一(甲基)丙烯酸酯、羥基特戊酸新戊二醇二 (甲基)丙烯酸酯、三羥甲基丙烷三(甲基)丙烯酸酯、 異戊四醇三〔甲基)丙烯酸酯、異戊四醇四(甲基)丙燒 酸酯、二(三經甲基丙烷)四(甲基)丙烯酸酯' 二異戊 四醇五(甲基)丙烯酸酯、二異戊四醇六(甲基)丙烯酸 (請先閲讀背面之注意事項再填寫本頁) 1裝. 訂Rio R11 (5) where R8 represents a hydrogen atom or a methyl group, R9 represents an alkylene group having 2 to 8 carbon atoms, r is an integer from 0 to 8, and R1Q and R11 represent a hydrogen atom or having Alkyl of 1 to 6 carbon atoms. Examples of commercially available products printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs of these monofunctional compounds include Aronix M101, M102, M110, M113, M114, M117, M120, M152, M154, M5300, M5400, M5500, M5600 ( (Manufactured by Toagosei Co., Ltd.), KAYARAD TC-110S, R128H, R629, R644 (manufactured by Nippon Kayaku Co., Ltd), IPAA, AIB, SBAA, TBA, IAAA, HEXA, CHA, NOA, IAA , INAA, LA, TDA, MSAA, CAA, HDAA, LTA, STA, ISAA-1, 〇DAA, NDAA, IBXA, ADAA, TCDA, 2-MTA, DMA, Viscoat # 150, # 150D, # 155, # 158 # 160, # 190, # 190D, # 192, # 193, # 220, # 320, # 2311HP, # 2000, # 2100, # 2150, # 2180, MTG (manufactured by Osaka Organic Chemical Industry Co., Ltd.- 18- This paper size is in accordance with Chinese National Standard (CNS) A4 specification (210X297 mm) 574339 A7 B7 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 5. Description of the invention (16)), NK Ester M-20G, M-40G , M-90G, M-230G, CB-1, SA, S, AMP-10G, AMP-20G, AMP-60G, AMP-90G, A-SA, NLA (manufactured by Shin- Nakamura Chemical Co., Ltd.) ACM〇 (manufactured by Kojin Co., Ltd.), light acrylate IA-A, LA, SA, B0-A, EC-A, MTG-A, DPM-A, PO-A, P-2O0A, THF- A, IB-XA, HOA-MS, HOA-MPL, HOA-MPE, HOA-HH, IO-A, BZ-A, NP-EA, NP-10EA, HOB-A, FA-108, epoxy ester M -600A, light ester PM (manufactured by Kyoeisha Chemical Co., Ltd.), FA-511, FA-512A, FA-513A (manufactured by Hitachi Chemical Co., Ltd.), AR-100, MR-100, MR-200 , MR-260 (manufactured by Daihachi Chemical Co., Ltd.), JAMP-100, JAMP-514, JPA-514 (manufactured by Johoku Chemical Co., Ltd.) and the like. Examples of the aforementioned polyfunctional compound include ethylene glycol di (methyl) propionate, propylene glycol di (meth) propionate, 1,4-butanediol di (meth) acrylate, 1, 6 —Hexanediol di (meth) acrylate, 1,9-nonanediol di (fluorenyl) acrylate, di (ethylene glycol) di (meth) acrylate, tri (ethylene glycol) di ( Meth) acrylates' tetra (ethylene glycol) di (meth) acrylate, propylene glycol di (meth) acrylate, di (propylene glycol) di (meth) acrylate, tri (propylene glycol) di (methyl) Acrylates, polypropylene glycol di (meth) acrylates, neopentyl alcohol mono (meth) acrylates, neopentyl glycol di (meth) acrylates of hydroxyvaleric acid, trimethylolpropane tris (methyl) ) Acrylate, Isopentaerythritol tri [meth] acrylate, Isopentaerythritol tetra (meth) propionate, Di (trimethyl methacrylate) tetra (meth) acrylate 'Diisoprene Alcohol penta (meth) acrylate, diisopentaerythritol hexa (meth) acrylic acid (Please read the notes on the back first Fill in this page again) 1 Pack. Order

Jm 本紙張尺度適财目®家標準(CNS ) A4規格(210X297公餐) -19- 574339 A7 --- B7 五、發明説明(17) (請先閲讀背面之注意事項再填寫本頁) 醋、(甲基)丙烯酸三羥甲基丙烷三氧乙酯、(甲基)丙 矯酸Η羥甲基丙烷多氧乙酯、(甲基)丙烯酸三羥甲基丙 院三氧丙酯、(甲基)丙烯酸三羥甲基丙烷多氧乙酯、三 (2 —羥基乙基)異氰尿酸酯二(甲基)丙烯酸酯、三( 2 -羥基乙基)異氰尿酸酯三(甲基)丙烯酸酯、氧化乙 燃加成雙酚Α二(甲基)丙烯酸酯、氧化乙烯加成雙酚ρ 一(甲基)丙燒酸酯、氧化丙嫌加成雙酣A二(甲基)丙 烯酸酯、氧化丙烯加成雙酚F二(甲基)丙燒酸酯、三環 癸烷二曱醇二(甲基)丙烯酸酯、雙酚A二環氧基二(甲 基)丙烯酸酯、雙酚F二環氧基二(甲基)丙烯酸酯、雙 〔2 -(甲基)丙烯醯氧乙基〕磷酸酯、雙〔2 一(甲基 )丙烯醯氧丙基〕磷酸酯、三〔2 -(甲基)丙烯醯氧乙 基〕磷酸酯、及其類者。 經濟部智慧財產局員工消費合作社印製Jm The paper size is suitable for households ® Standards (CNS) A4 (210X297 meals) -19- 574339 A7 --- B7 V. Description of the invention (17) (Please read the precautions on the back before filling this page) Vinegar , Trimethylolpropane trioxyethyl (meth) acrylate, trimethylolpropane polyoxyethyl (meth) propionate, trimethylolpropane trimethacrylate (meth) acrylate, ( Trimethylolpropane polyoxyethyl methacrylate, tris (2-hydroxyethyl) isocyanurate di (meth) acrylate, tris (2-hydroxyethyl) isocyanurate tri ( Methacrylic acid esters, bisphenol A di (meth) acrylate added with ethylene oxide, ethylene oxide bisphenol ρ mono (meth) propionate, propylene oxide bispyridine A bis (a) Base) acrylate, propylene oxide addition of bisphenol F di (meth) propionate, tricyclodecanediethanol di (meth) acrylate, bisphenol A diepoxy di (meth) acrylic acid Ester, bisphenol F diepoxy di (meth) acrylate, bis [2- (meth) acryloxyethyl] phosphate, bis [2-mono (meth) acryloxy] Yl] phosphate, tris [2 - (meth) Bing Xixi oxo ethyl] phosphate, and by categories. Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs

此等多官能基化合物之市售產物實例係包括SA- 1002、 SA-2006 、 SA-2007 、 SA-4100 、 SA-5001 、 SA-6000 、 SA-7600 、SA-8000、SA-9000(Mitsubishi Chemical Corp.製造)、 Viscoat #195, #195D, #214HP, #215, #215D, #230, #230D, #260,#295,#295D,#300,#310HP,#310HG, #312, #335HP, #335D, #360, GPT, #400, #540, #700, GPT, Viscoat 3PA (Osaka Organic Chemical Industry Co·,Ltd.製造),KAYARAD MANDA, R-526, NPGDA, PEG400DA, R-167, HX-220, HX-620, R-551, R-712, R-604, R-684, GPO-303, TMPTA, THE-330, TPA-320, TPA-3 30, PET-30, RP-1040, T-1420, DPHA, D-310, D-330, DPCA-20, DPCA-30, DPCA-60, DPCA-120 (Nippon 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公釐) .20- 574339 A7 B7 五、發明説明(18 ) (請先閲讀背面之注意事項再填寫本頁)Examples of commercially available products of these multifunctional compounds include SA-1002, SA-2006, SA-2007, SA-4100, SA-5001, SA-6000, SA-7600, SA-8000, SA-9000 (Mitsubishi (Manufactured by Chemical Corp.), Viscoat # 195, # 195D, # 214HP, # 215, # 215D, # 230, # 230D, # 260, # 295, # 295D, # 300, # 310HP, # 310HG, # 312, # 335HP, # 335D, # 360, GPT, # 400, # 540, # 700, GPT, Viscoat 3PA (manufactured by Osaka Organic Chemical Industry Co., Ltd.), KAYARAD MANDA, R-526, NPGDA, PEG400DA, R-167 , HX-220, HX-620, R-551, R-712, R-604, R-684, GPO-303, TMPTA, THE-330, TPA-320, TPA-3 30, PET-30, RP- 1040, T-1420, DPHA, D-310, D-330, DPCA-20, DPCA-30, DPCA-60, DPCA-120 (Nippon This paper size applies to China National Standard (CNS) A4 specification (210X297 mm) .20- 574339 A7 B7 V. Description of Invention (18) (Please read the precautions on the back before filling this page)

Kayaku Co·,Ltd.製造),Aronix M_210,M-208,M-215,M-220, M-225,M233,M-240,M-245,M-260,M-270,M-305,M-309, M-310,M-315,M-320,M-350,M-360,M-400,M-408,M-450 (Toagosei Co·,Ltd.製造),SR-212,SR-213,SR- 355 (Sartomer Co·,Ltd·製造),SP- 1 506,SP- 1 507,SP- 1 509,SP-1519-1,SP-1 563,SP-2500,VR60,VR77,VR90 (Showa Highpolymer Co·, Ltd.製造)、輕酯P-2M (Kyoeisha Chemical Co·,Ltd·製造), EB-169,ΕΒ·179,EB-3603,R-DX63 1 82 (Diacel-UCB Co.,Ltd· 製造)及其類者。 可添加除組份(D )以外之感光起始劑於本發明組合 物中。該其他感光起始劑之實例係包括3 -曱基乙醯苯、 經濟部智慧財產局員工消費合作社印製 2,2 -二甲氧基一 2 -苯基乙醯苯、咕噸酮、芴酮、苯 甲醛、芴、蒽醌、三苯胺、卡唑' 3 —甲基乙醯苯、二苯 基甲酮、4一氯二苯基甲酮、4,4’ 一二甲氧基二苯基 甲酮、4,4’ 一二甲基二苯基甲酮、安息香乙醚、安息 香丙醚、Mi c 1 i 1 e r氏酮、二甲醇縮苄酮、1 一( 4_異丙苯基)一2 -羥基一 1 一甲基丙—1_酮、1 一 (4 一十二碳基苯基)一 2 —羥基一 2 —甲基丙-1—酮 、4 - (2 —羥基乙氧基)苯基一(2 -羥基一 2 -丙基 )酮、2 —甲基—1—〔4 一(甲硫基)苯基〕一 2 —嗎 啉一丙一 1 一酮、2,4,6 -三甲基苄醯基苯基膦酸酯 、氧化2,4,6 -三甲基苄醯基二苯基膦、2 -苄基一 2 -二曱基胺基一 1 一(4 一嗎啉苯基)一丁 — 1 一酮、 氧化雙(2 ,6 —二甲氧基苄醯基)一 2 ,4 ,4 —三甲 -21 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210、〆297公釐) 574339 A7 B7 五、發明説明(19) (請先閲讀背面之注意事項再填寫本頁) 基戊基膦、苄醯甲酸甲酯、噻噸酮、二乙基噻噸酮、2 -異丙基噻噸酮、2 -氯基噻噸酮、及寡聚〔2 —羥基—2 一甲基一 1 一 〔4 一(1—甲基乙烯基)苯基〕丙酮。此 等化合物可用以增加表面固化性及該組合物之固化速度。 若與化合物(D )組合使用,則此等其他感光起始劑相對 於該其他感光起始劑及化合物(D )之組合含量較佳係最 高達70重量百分比。 此等其他感光起始劑之市售產物的實例係包括 IRGACURE 261、369、907、819、1700、1 800、1 850、2959 、CGI-403、Darocur 95 3、1116、1 664、2273(Ciba Specialty Chemicals Co.,Ltd.製造)、Lucirin TP〇,LR8728,LR8893 (BASF 製造)、Ubecryl P36 (UCB 製造)、VICURE5 5 (Akzo 製 造)、ESACURE KIP 100F,KIP 150 (Lamberti 製造)、 KAYACURE CTX,DETX, BP-100, BMS,及 2-EAQ (Nippon Kayaku Co·,Ltd·製造)。 經濟部智慧財產局員工消費合作社印製 除組份(E )以外之矽烷偶聯劑可添加於本發明組合 物中。矽烷偶聯劑之實例係包括T -氫碳基丙基甲基單乙 氧基矽烷、7 -氫硫基丙基二乙氧基矽烷、T -氫硫基丙 基三乙氧基矽烷、/3 -氫硫基乙基單乙氧基矽烷、/3 -氫 硫基乙基三乙氧基矽烷、N -(2 -胺基乙基)一 3 -胺 基丙基甲基二曱氧基矽烷、N -(2 —胺基乙基)一 3 -胺基丙基三曱氧基矽烷、r -胺基丙基三乙氧基矽烷、τ -縮水甘油氧基丙基三甲氧基矽烷、r -縮水甘油氧基丙 基甲基二甲氧基矽烷、2 -(3,4 一環氧基環己基)乙 -22- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 __B7 五、發明説明(20 ) (請先閲讀背面之注意事項再填寫本頁) 基二甲氧基砍院、T -氯基丙基甲基二甲氧基砂院、r__ 氯丙基三甲氧基矽烷、及T -甲基丙烯醯氧丙基三甲氧基 矽烷。此等矽烷偶聯劑之市售產品的實例係包括Sila_Ace S310、 S311、 S320、 S321、 S330、 S510、 S520、 S530、 S610 、S620、S710(Chisso Corp·製造)、SH6060、SZ6023、 SZ6030、SH6040、SH6076、SZ6083(T〇ray-D〇w Corning Silicone Co., Ltd·製造)、KBM403、KBM503、KBM602、 KBM603、KBE903 (Shin-Etsu Chemical Industries Co·,Ltd.製 造)。 經濟部智慧財產局員工消費合作社印製 可添加除了含有丙烯酸基之化合物以外的輻射可聚合 化合物於本發明組合物中。該化合物之實例係包括N -乙 烯基吡咯烷酮、N -乙烯基己內醯胺、乙酸乙烯酯、丙酸 乙烯酯、苯乙烯、二乙烯基苯、及不飽和聚酯。前述不飽 和聚酯包括具有輻射可聚合不飽和雙鍵之二羧酸與醇類的 酯類。具有輻射可聚合不飽和雙鍵之二羧酸的實例係包括 順丁烯二酸酐、衣康酸、及反丁烯二酸。醇類之實例係包 括單羥基醇,例如甲醇、乙醇、正丙醇、異丙醇、正丁醇 、異丁醇、第二丁醇、第三丁醇、正己醇、環己醇、及2 一乙基己醇;(多)乙二醇諸如乙二醇、二(乙二醇)、 及三(乙二醇);(多)丙二醇諸如丙二醇、二(丙二醇 )、及三(丙二醇)·,二羥基醇諸如1 ,6 -己二醇;及 三羥基醇諸如甘油及三羥甲基丙烷。 而且,可添加環氧樹脂、聚醯胺、聚醯胺醯亞胺、聚 胺基甲酸酯、聚丁二烯、氯丁二烯、聚醚、聚酯、戊二烯 -23- 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 574339 A7 B7 五、發明説明(21 ) (請先閱讀背面之注意事項再填寫本頁) 衍生物、SB S (苯乙烯/ 丁二烯/苯乙烯嵌段共聚物) 、氫化SBS、S I S (苯乙烯/異戊間二烯/苯乙烯嵌 段共聚物)、石油樹脂、二甲苯樹脂、酮樹脂、含氟之寡 聚物、矽酮型寡聚物、聚醚型寡聚物、及其類者於本發明 化合物中,以作爲其他添加劑。 而且,可添加塗料添加劑諸如抗氧化劑、紫外光U V 吸收劑、光安定劑、防老化劑、消泡劑、勻平劑、抗靜電 劑、界面活性劑、防腐劑、熱-聚合抑制劑、增塑劑、及 潤溼改良劑於本發明組合物中。抗氧化劑之實例係包括 Irganox 245、259、565、1010、1 035、1076、1081、1098、 1 222、及 1 330 (Ciba Specialty Chemicals Co.,Ltd.製造)。 紫外光U V吸收劑之實例係包括苯并三唑型及三畊型 紫外光U V吸收劑。此等紫外光U V吸收劑之市售產品包 括 Tinuvin P、234、320、326、327、328、213、400 (Ciba Specialty Chemicals Co.,Ltd·製造)、Sumisorb 110、130、 140、220、250、300 ' 320、340、350、及 400 (Sumitomo Chemical Industries Co.,Ltd.製造)。 經濟部智慧財產局員工消費合作社印製 光安定劑之實例係包括Tinuvin 144、292、622LD (Ciba Specialty Chemicals Co·,Ltd·製造)、Sanol LS440、LS770 (S a n k y o C o ·, L t d ·製造)及 s u m i s o r b T M - 0 6 1 (S u m i t o m o(Made by Kayaku Co., Ltd.), Aronix M_210, M-208, M-215, M-220, M-225, M233, M-240, M-245, M-260, M-270, M-305, M-309, M-310, M-315, M-320, M-350, M-360, M-400, M-408, M-450 (manufactured by Toagosei Co., Ltd.), SR-212, SR -213, SR-355 (manufactured by Sartomer Co., Ltd.), SP-1 506, SP-1 507, SP-1 509, SP-1519-1, SP-1 563, SP-2500, VR60, VR77, VR90 (manufactured by Showa Highpolymer Co., Ltd.), light ester P-2M (manufactured by Kyoeisha Chemical Co., Ltd.), EB-169, EB · 179, EB-3603, R-DX63 1 82 (Diacel-UCB Co ., Ltd.) and others. A photosensitive initiator other than the component (D) may be added to the composition of the present invention. Examples of such other photoinitiators include 3 -fluorenylacetophenone, printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs, 2,2-dimethoxy-2-phenylethylacetophenone, galanthone, pyrene Ketones, benzaldehyde, pyrene, anthraquinone, triphenylamine, carbazole '3-methylacetophenone, diphenylmethanone, 4-chlorodiphenylmethanone, 4,4'-dimethoxydiphenyl Methyl ketone, 4,4 'dimethyldiphenyl ketone, benzoin ether, benzoin propyl ether, Mi c 1 i 1 er ketone, dimethanol ketal, 1- (4-cumene) 1 2-hydroxy-1 1-methylpropan-1-one, 1 1- (4-dodecylphenyl) -1 2-hydroxy-2 2-methylpropan-1-one, 4-(2-hydroxyethoxy Phenyl) phenyl mono (2-hydroxy-2 propyl) ketone, 2-methyl-1- [4-mono (methylthio) phenyl] 2- 2-morpholine propyl 1-one, 2, 4 , 6-trimethylbenzylfluorenylphenyl phosphonate, 2,4,6-trimethylbenzylfluorenyldiphenylphosphine, 2-benzyl-2-difluorenylamino-1 1- (4 Monomorpholine phenyl) monobutan-1 monoketone, bis (2,6-dimethoxybenzylfluorenyl) -2, 4, 4 — Top 3-21-This paper size applies to Chinese National Standard (CNS) A4 specifications (210, 〆297 mm) 574339 A7 B7 V. Description of invention (19) (Please read the notes on the back before filling this page ) Isopentylphosphine, methyl benzamidine formate, thioxanthone, diethylthioxanthone, 2-isopropylthioxanthone, 2-chlorothioxanthone, and oligo [2-hydroxy-2 Methyl 1- [4-((1-methylvinyl) phenyl] acetone. These compounds can be used to increase the surface curability and the curing speed of the composition. If used in combination with compound (D), the content of these other photoinitiators relative to the combination of the other photoinitiators and compound (D) is preferably up to 70% by weight. Examples of commercially available products of these other photosensitive initiators include IRGACURE 261, 369, 907, 819, 1700, 1 800, 1 850, 2959, CGI-403, Darocur 95 3, 1116, 1 664, 2273 (Ciba Specialty Chemicals Co., Ltd.), Lucirin TP〇, LR8728, LR8893 (manufactured by BASF), Ubecryl P36 (manufactured by UCB), VICURE5 5 (manufactured by Akzo), ESACURE KIP 100F, KIP 150 (manufactured by Lamberti), KAYACURE CTX, DETX, BP-100, BMS, and 2-EAQ (manufactured by Nippon Kayaku Co., Ltd.). Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs Silane coupling agents other than component (E) may be added to the composition of the present invention. Examples of the silane coupling agent include T-hydrocarbonpropylmethylmonoethoxysilane, 7-hydrothiopropyldiethoxysilane, T-hydrothiopropyltriethoxysilane, / 3-Hydroxythioethylmonoethoxysilane, / 3-hydrothioethyltriethoxysilane, N- (2-aminoethyl) -3-aminopropylmethyldioxo Silane, N- (2-aminoethyl) -3-aminopropyltrimethoxysilane, r-aminopropyltriethoxysilane, τ-glycidyloxypropyltrimethoxysilane, r -Glycidyloxypropylmethyldimethoxysilane, 2-(3,4 monoepoxycyclohexyl) ethyl-22- This paper size is applicable to China National Standard (CNS) A4 (210X297 mm) 574339 A7 __B7 V. Description of the invention (20) (Please read the precautions on the back before filling in this page) Didimethoxy cutting institute, T-chloropropylmethyldimethoxy sand institute, r__chloropropyl Trimethoxysilane and T-methacryloxypropyltrimethoxysilane. Examples of commercially available products of these silane coupling agents include Sila_Ace S310, S311, S320, S321, S330, S510, S520, S530, S610, S620, S710 (made by Chisso Corp.), SH6060, SZ6023, SZ6030, SH6040 , SH6076, SZ6083 (manufactured by Toray-Dow Corning Silicone Co., Ltd.), KBM403, KBM503, KBM602, KBM603, KBE903 (manufactured by Shin-Etsu Chemical Industries Co., Ltd.). Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs. A radiation polymerizable compound other than the compound containing an acrylic group may be added to the composition of the present invention. Examples of the compound include N-vinylpyrrolidone, N-vinylcaprolactam, vinyl acetate, vinyl propionate, styrene, divinylbenzene, and unsaturated polyester. The aforementioned unsaturated polyesters include esters of dicarboxylic acids and alcohols having a radiation polymerizable unsaturated double bond. Examples of dicarboxylic acids having a radiation polymerizable unsaturated double bond include maleic anhydride, itaconic acid, and fumaric acid. Examples of alcohols include monohydric alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, second butanol, third butanol, n-hexanol, cyclohexanol, and 2 Monoethylhexanol; (poly) ethylene glycols such as ethylene glycol, di (ethylene glycol), and tris (ethylene glycol); (poly) propylene glycols such as propylene glycol, di (propylene glycol), and tri (propylene glycol) · Dihydroxy alcohols such as 1,6-hexanediol; and trihydroxy alcohols such as glycerol and trimethylolpropane. In addition, you can add epoxy resin, polyamide, polyamide imidate, polyurethane, polybutadiene, chloroprene, polyether, polyester, pentadiene-23- this paper Standards are applicable to Chinese National Standard (CNS) A4 (210 X 297 mm) 574339 A7 B7 V. Description of the invention (21) (Please read the notes on the back before filling this page) Derivatives, SB S (styrene / butylene Diene / styrene block copolymer), hydrogenated SBS, SIS (styrene / isoprene / styrene block copolymer), petroleum resin, xylene resin, ketone resin, fluorine-containing oligomer, Silicone oligomers, polyether oligomers, and the like are among the compounds of the present invention as other additives. Moreover, coating additives such as antioxidants, ultraviolet light absorbers, light stabilizers, anti-aging agents, defoamers, leveling agents, antistatic agents, surfactants, preservatives, thermal-polymerization inhibitors, Plasticizers and wetting improvers are used in the compositions of the present invention. Examples of the antioxidant include Irganox 245, 259, 565, 1010, 1 035, 1076, 1081, 1098, 1 222, and 1 330 (manufactured by Ciba Specialty Chemicals Co., Ltd.). Examples of the ultraviolet light UV absorber include benzotriazole-type and three-till UV light absorbers. Commercial products of these ultraviolet light UV absorbers include Tinuvin P, 234, 320, 326, 327, 328, 213, 400 (manufactured by Ciba Specialty Chemicals Co., Ltd.), Sumisorb 110, 130, 140, 220, 250 , 300 '320, 340, 350, and 400 (manufactured by Sumitomo Chemical Industries Co., Ltd.). Examples of light stabilizers printed by employees' cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs include Tinuvin 144, 292, 622LD (manufactured by Ciba Specialty Chemicals Co., Ltd.), Sanol LS440, LS770 (manufactured by Ankyo Co., L td.) ) And sumisorb TM-0 6 1 (S umitomo

Chemical Industries Co.,Ltd.製造)。 防老化劑之實例係包括酚型防老化劑、烯丙胺型防老 化劑、及酮胺型防老化劑。此等防老化劑之市售品係包括 Antigene W,S,P,3C,6C,RD-G,FR,及 AW (Sumitomo -24- 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X297公羞) 574339 A7 B7 五、發明説明(22)(Manufactured by Chemical Industries Co., Ltd.). Examples of the anti-aging agent include a phenol type anti-aging agent, an allylamine type anti-aging agent, and a ketoamine type anti-aging agent. Commercially available products of these anti-aging agents include Antigene W, S, P, 3C, 6C, RD-G, FR, and AW (Sumitomo -24- This paper is in accordance with China National Standard (CNS) A4 (210 X297) Public shame) 574339 A7 B7 V. Description of invention (22)

Chemical Industries Co.,Ltd.製造)。 (請先閲讀背面之注意事項再填寫本頁) 消泡劑之實例係包括不含矽原子或氟原子之有機共聚 物,諸如尸1(^:^11八(:-202、八(:-300、八(:-303、八0-326?、八(:- 900、AC-1190、AC-2000 (Kyoeisha Chemical Co·,Ltd.製造) 、含有矽原子之消泡劑諸如Flowlen AC-901、AC-950、AC-1140、 A〇-3、 A〇-4〇H (Kyoeisha Chemical Co·, Ltd· 製造 )、 FS- 1 265、SH200、SH5500、SC5540、SC5570、F-l、SD5590 (Toray-Dow Corning Silicone Co.,Ltd.製造)、及含有氟原子 之消泡劑諸如 MEGAFAC F-142D、F-144D、F-178K、F-179、 F- 8 1 5 (Dainippon Ink and Chemicals, Inc.製造)。 勻平劑之實例係包括 Polyflow No.7,No.38,No.50E,S, 75,No.75, No.77, No.90, No.95, No.300, No.460, ATF,^ KL-245(Kyoeisha Chemical Co·,Ltd.製造)。此等添加劑之添加 量可視情況決定,其限制條件爲不對本發明目的有負面之 影響。 經濟部智慧財產局員工消費合作社印製 本發明組合物之黏度以10 — 10,〇〇〇mPa · s爲佳,50 — 5,OOOmPa · s更佳,尤其是 150 — 2,000mPa.s〇 較佳係添加各組份使形成之固化產物的玻璃態化溫度 介於—3 0至2 0 0 °C之範圍內,以由〇至1 2 0°C爲佳 。若玻璃態化溫度太低,則固化產物可能在夏天或在高溫 下密閉日照房中軟化,使得基材可能因爲膠黏性降低而位 移或移動。若玻璃態化溫度太高,則膠黏性可能不足或該 基材可能在掉落或彎曲時斷裂。 本紙張尺度適用中g]國家標準(CNS ) A4規格(210X 297公釐) -25 - 574339 A7 B7 五、發明説明(23) (請先閱讀背面之注意事項再填寫本頁) 本發明所使用之”玻璃態化溫度”意指在1 0振盪頻 率下使用動態黏彈性測量裝置測量時,損失正切値( tan5)之最大値。 本發明組合物較佳係藉著照射紫外光、可見光、電子 束、或其類者而固化。例如,本發明化合物在施加於基材 之間使得膠黏層之厚度爲1 0 - 1 0 0微米時,使用劑量 爲5 0 - 2 0 0 0毫焦耳/厘米2之金屬鹵化物燈照射該化 合物,即可輕易地固化。 本發明化合物之感光固化產物較佳係具有優越之透明 性。例如,固化組合物之6 0微米厚層在6 0 0 - 7 0 0 奈米下具有9 0百分比或更高之透光度。若該透光度低於 9 0百分比,則光碟之外觀可能受損。而且,用以讀取儲 存於磁碟中之資料的光係因固化產物之膠黏層而減少,因 而阻礙讀取操作。因此,較佳係藉著組合各組份,使得該 固化產物之透光度介於前述範圍內,而製備本發明組合物 0 經濟部智慧財產局員工消費合作社印製 較佳係添加各組份,使得本發明組合物之感光固化產 物在25 °C下具有1 · 5 1 - 1 · 70之折射率。若感光 固化產物之折射率超出此範圍,則在讀取儲存磁碟中之資 料時,可能產生問題。 本發明化合物對於各式各樣之材料具有良好膠黏性, 包括塑料諸如聚碳酸酯(P C )及聚甲基丙烯酸甲酯( PMMA)、金屬(例如黃金、銀、及錦)、及無機化合 物(例如玻璃)。因此,該組合物適於作爲供光碟使用之 -26- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(24) 膠黏劑。 實施例 使用實施例描述本發明,其應不限制本發明。 胺基甲酸酯丙烯酸酯(組份(A ))之合成: 合成例1 裝置有攪拌器及溫度計之1公升可分離燒瓶中置入 209克異佛爾酮二異氰酸酯、0 · 2克3,5 —二—第 三丁基一4一羥基甲苯、及〇.8克二月桂酸二正丁基錫 。該混合物經攪拌,且於冷水浴中於乾燥空氣中冷卻至 1 0 °C。於1 0 — 3 5 °C下緩緩添加1 〇 9克丙烯酸2 — 羥基乙酯歷經一小時,並使之反應。添加3 0 5 . 5克平 均分子量爲 6 5 0 之聚 丁二醇(Mitsubishi Chemical Corp. 製造之” P T M G 6 5 0 ” )之後,該混合物於4 0 -6 0 t下於攪拌下進行反應5小時。去除反應產物,以得 到數量平均分子量爲1 3 0 0之胺基甲酸酯丙烯酸酯( A 1 )。 合成例2 使用與合成例1相同之方式得到數量平均分子量爲 1650之胺基甲酸酯丙烯酸酯(A2),不同處使用4 8 0克平均分子量爲1 0 〇 0之聚丁二醇(Mitsubishi Chemical Corp.製造之” P T M G 1 0 〇 〇 ’’ )取代合成 (請先閲讀背面之注意事項再填寫本頁) ¾衣·(Manufactured by Chemical Industries Co., Ltd.). (Please read the notes on the back before filling this page.) Examples of defoamers include organic copolymers that do not contain silicon or fluorine atoms, such as corpse 1 (^: ^ 11 eight (: -202, eight (:- 300, eight (: -303, eight 0-326 ?, eight (: -900, AC-1190, AC-2000 (manufactured by Kyoeisha Chemical Co., Ltd.), defoamers containing silicon atoms such as Flowlen AC-901 , AC-950, AC-1140, A〇-3, A〇-4〇H (manufactured by Kyoeisha Chemical Co., Ltd.), FS-1 265, SH200, SH5500, SC5540, SC5570, Fl, SD5590 (Toray- (Dow Corning Silicone Co., Ltd.), and defoamers containing fluorine atoms such as MEGAFAC F-142D, F-144D, F-178K, F-179, F- 8 1 5 (Dainippon Ink and Chemicals, Inc. Manufacturing) Examples of leveling agents include Polyflow No. 7, No. 38, No. 50E, S, 75, No. 75, No. 77, No. 90, No. 95, No. 300, No. 460 , ATF, ^ KL-245 (manufactured by Kyoeisha Chemical Co., Ltd.). The addition amount of these additives can be determined according to the situation, and its limitation is not to have a negative impact on the purpose of the present invention. Making the invention The viscosity of the composition is preferably from 10 to 10,000 mPa · s, more preferably from 50 to 5,000 mPa · s, especially from 150 to 2,000 mPa · s. Preferably, each component is added so as to form a cured product. The glass transition temperature is in the range of -30 to 200 ° C, preferably from 0 to 120 ° C. If the glass transition temperature is too low, the cured product may be in summer or at high temperatures Softening in a closed sunlight room may cause the substrate to be displaced or moved due to reduced adhesiveness. If the glass transition temperature is too high, the adhesiveness may be insufficient or the substrate may break when dropped or bent. Dimensions of this paper In application g] National Standard (CNS) A4 specification (210X 297 mm) -25-574339 A7 B7 V. Description of the invention (23) (Please read the precautions on the back before filling this page) The "glass" used in the present invention “State temperature” means the maximum value of the loss tangent (tan5) when measured using a dynamic viscoelasticity measuring device at a frequency of 10 oscillations. The composition of the present invention is preferably irradiated with ultraviolet light, visible light, electron beam, or Others are cured. For example, when the compound of the present invention is applied between substrates so that the thickness of the adhesive layer is 10 to 100 micrometers, a metal halide lamp with a dose of 50 to 2000 millijoules / cm2 is used to irradiate the compound. Compounds, which can be easily cured. The photosensitive cured product of the compound of the present invention preferably has superior transparency. For example, a 60 micron thick layer of a cured composition has a light transmittance of 90 percent or more at 600 to 700 nanometers. If the light transmittance is less than 90%, the appearance of the disc may be damaged. Moreover, the light used to read the data stored in the magnetic disk is reduced due to the adhesive layer of the cured product, which hinders the reading operation. Therefore, it is better to prepare the composition of the present invention by combining the components so that the light transmittance of the cured product is within the aforementioned range. , So that the photosensitive cured product of the composition of the present invention has a refractive index of 1 · 5 1-1 · 70 at 25 ° C. If the refractive index of the photosensitive cured product exceeds this range, problems may occur when reading the data in the storage disk. The compounds of the present invention have good adhesion to a wide variety of materials, including plastics such as polycarbonate (PC) and polymethyl methacrylate (PMMA), metals (such as gold, silver, and brocade), and inorganic compounds (E.g. glass). Therefore, the composition is suitable for use as an optical disc. -26- This paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 574339 A7 B7 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 24) Adhesive. Examples The present invention is described using examples, which should not limit the present invention. Synthesis of urethane acrylate (component (A)): Synthesis Example 1 A liter separable flask equipped with a stirrer and a thermometer was placed in 209 g of isophorone diisocyanate, 0.2 g of 3, 5-Di-tert-butyl-4-hydroxytoluene and 0.8 g of di-n-butyltin dilaurate. The mixture was stirred and cooled to 10 ° C in dry air in a cold water bath. Slowly add 109 g of 2-hydroxyethyl acrylate at 10 to 35 ° C over an hour and allow it to react. After adding 3.05 g of polybutylene glycol ("PTMG 6 50" manufactured by Mitsubishi Chemical Corp.) having an average molecular weight of 6 50, the mixture was reacted under stirring at 40-60 t. 5 hour. The reaction product was removed to obtain a urethane acrylate (A 1) having a number average molecular weight of 1,300. Synthesis Example 2 A urethane acrylate (A2) having a number average molecular weight of 1650 was obtained in the same manner as in Synthesis Example 1, except that 480 g of polybutanediol (Mitsubishi) having an average molecular weight of 1,000 was used. "PTMG 1 0 00" manufactured by Chemical Corp.) instead of synthesis (Please read the precautions on the back before filling this page)

、1T d 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -27- 574339 A7 B7 五、發明説明(25) 例1所使用之聚丁二醇。 (請先閲讀背面之注意事項再填寫本頁) 實施例1 在裝置有攪拌器之反應器中置入4 0克在合成例1中 合成之胺基甲酸酯丙烯酸酯(A 1 )、2 0克丙烯酸4 -經基丁酯(C 1 )( Osaka Organic Chemical Industry Co., Ltd.製造之” 4HBA” )、15克氧化乙烯加成雙酚A二 丙儲酸酯(F 1 ) (Showa Highpolymer Co·,Ltd.製造之” VR77” ) 、25克乙二醇二丙烯酸酯(F2)(、 1T d This paper size applies to Chinese National Standard (CNS) A4 specification (210X297mm) -27- 574339 A7 B7 V. Description of the invention (25) Polybutylene glycol used in Example 1. (Please read the precautions on the back before filling this page) Example 1 Put 40 g of urethane acrylate (A 1), 2 synthesized in Synthesis Example 1 in a reactor equipped with a stirrer 0 g of 4-butyl acrylate (C 1) ("4HBA" manufactured by Osaka Organic Chemical Industry Co., Ltd.), 15 g of ethylene oxide added to bisphenol A dipropionate (F 1) (Showa "VR77" manufactured by Highpolymer Co., Ltd.), 25 g of ethylene glycol diacrylate (F2) (

Kyoeosha Chemical Co·,Ltd.製造之”輕丙烯酸酯 4 E G A ” )、3克2 ,2 —二甲氧基—1 ,2 —二苯基乙一1 一 酮(Ciba Specialty Chemicals Co·,Ltd.製造之 ” Irgacure 651 ” )、3克2 —羥基—2 —甲基一 1—苯基丙一 1—酮("Light Acrylate 4 EGA" manufactured by Kyoeosha Chemical Co., Ltd.), 3 g of 2,2-dimethoxy-1,2-diphenylethylene-1 monoone (manufactured by Ciba Specialty Chemicals Co., Ltd.) "Irgacure 651"), 3 grams of 2-hydroxy-2-methyl-1,1-phenylpropan-1-one (

Ciba Specialty Chemicals Co·,Ltd·製造之” Darocur 1173” 經濟部智慧財產局員工消費合作社印製 )、〇 · 5克二甲基胺基苯甲酸乙酯(Nippon Kayaku Co., Ltd.製造之” KAYACURE EPA” )、1克r —氫硫基丙基三 甲氧基石夕院(Toray-Dow Corning Silicone Co.,Ltd.製造之” SH6062 ” )、及0 . 3克2,2 —硫二伸乙基雙〔 3 -(3,5 -二一第三丁基一 4 一羥基苯基)丙酸酯) (CibaSpecialty Chemicals Co.,Ltd.製造之 ” Irganox 1035” )。該混合物於5 0 t下攪拌一小時,以得到實施例1之 組合物。"Darocur 1173" manufactured by Ciba Specialty Chemicals Co., Ltd. (printed by the Consumer Cooperative of Intellectual Property Bureau, Ministry of Economic Affairs), 0.5 g of dimethylaminobenzoate (manufactured by Nippon Kayaku Co., Ltd. " KAYACURE EPA "), 1 gram of r-Hydroxythiopropyltrimethoxy-Shi Xiyuan (" SH6062 "manufactured by Toray-Dow Corning Silicone Co., Ltd.), and 0.3 grams of 2,2-thiodiethylene glycol Bis [3- (3,5-di-tertiary-butyl-4 monohydroxyphenyl) propionate) ("Irganox 1035" manufactured by Ciba Specialty Chemicals Co., Ltd.). The mixture was stirred at 50 t for one hour to obtain the composition of Example 1.

實施例2 - Q -28- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 574339 A7 B7 五、發明説明(26 ) (請先閲讀背面之注意事項再填寫本頁) 實施例2 - 9使用與實施例1相同之方式製備用以形 成塗膜之組合物,不同處係改變組份。表1所示之各組份 如下。表1中之組份的用量係以重量份數表示。 組份(B ) B1 :對—二甲基胺基苯甲酸乙酯(Nippon Kayaku Co., Ltd.製造之” KAYACUREEPA” ) B 2 :二甲基胺基苯甲酸異戊酯(Nippon Kayaku Co_,Ltd· 製造之” KAYACUREDMBI” ) 組份(C ) C 1 :丙烯酸 4 —羥基丁酯(Osaka Organic ChemicalExample 2-Q -28- This paper size applies to Chinese National Standard (CNS) A4 (210X 297 mm) 574339 A7 B7 V. Description of Invention (26) (Please read the precautions on the back before filling this page) Implementation Examples 2 to 9 The composition for forming a coating film was prepared in the same manner as in Example 1, except that the composition was changed. The components shown in Table 1 are as follows. The amounts of the components in Table 1 are expressed in parts by weight. Component (B) B1: Ethyl p-dimethylaminobenzoate ("KAYACUREEPA" manufactured by Nippon Kayaku Co., Ltd.) B2: Isoamyl dimethylaminobenzoate (Nippon Kayaku Co., Ltd · "KAYACUREDMBI") Component (C) C 1: 4-Hydroxybutyl Acrylate (Osaka Organic Chemical

Industry Co.,Ltd.製造之 ” 4 — Η B A ” ) 組份(D ) D1 : 2 ,2 —二甲氧基一 1 ,2_二苯基乙一 1_酮( Ciba Specialty Chemicals Co.,Ltd.製造之” Irgacure 651” ) 經濟部智慧財產局員工消費合作社印製 D2 : 2 —羥基—2 -甲基_1 一苯基—丙—1-酮(Ciba Specialty Chemicals Co.,Ltd·製造之” Darcur 1173” ) 組份(E ) E 1 : r —氫硫基丙基三甲氧基石夕院(Toray-Dow Corning 3山(:〇1^0〇.,1^(1.製造之”3116062”) -29- 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 574339 A7 B7 五、發明説明(27) 其他紺份 (請先閲讀背面之注意事項再填寫本頁) 氧化乙烯加成雙酚A二(甲基)丙烯酸酯(Showa Highpolymer Co·,Ltd.製造之” V R — 7 7 ” ) 乙二醇二丙烯酸酯(Kyoeosha Chemical Co·,Ltd.製造之” 輕丙烯酸酯4 E G A ” ) 丙烯酸苯氧乙酯(Daiichi Kogyo Seiyaku Co·,Ltd.製造之” NewFrontierPHE” ) 2 -甲基-1 —〔4—(甲硫基)苯基〕—2 -嗎啉基— 丙—1 —酮(Ciba Specialty Chemicals Co·,Ltd·製造之” Irgacure 907” ) 2,2_硫二伸乙基雙〔3 -(3,5 -二一第三丁基一 4 —羥基苯基)丙酸酯〕(Ciba Specialty Chemicals Co·, Ltd·製造之 ” Irganox 1035” ) 邊緣固化性、耐濕熱性、及對所製備之組合物的基材 (實施例1 - 9之組合物)之膠黏性係如下文所述般地測 量及評估。 經濟部智慧財產局員工消費合作社印製 -30- 574339 A7 B7 五、發明説明(28) (請先閲讀背面之注意事項再填寫本頁) 膠黏性時,該組合物之邊緣固化性評斷爲”佳”。在照射 劑量爲2 5 0毫焦耳/厘米2之後不具有膠黏性時,該化合 物之邊緣固化性評斷爲”優”。 {21 耐濕熱性 使用如前述第(1 )項所述之方式,在5 0 0毫焦耳 /厘米2下照射該組合物,以使基材黏著。放置在9 〇 °c溫 度及9 8 %RH相對溼度下之等溫等濕器中之後,在膠黏 層或介於該膠黏劑與基材之間的界面上發現異常諸如發泡 或腐蝕時,該組合物之耐濕熱性評斷爲”差”。若未發現 異常,則該組合物之耐濕熱性評斷爲”佳”。 ill相對於某材之膠黏件 經濟部智慧財產局員工消費合作社印製 該組合物使用濺鍍方法施加於蒸發於P C基材上之鋁 膜或金膜上。該組合物於氮氛圍中照射1 〇 〇毫焦耳/厘 米2之劑量,得到厚度爲5 0微米之組合物固化薄膜。固化 之薄膜進行交叉切割玻璃紙帶剝離試驗。當鋁膜或金膜不 自P C基材移除時,該組合物之膠黏性評斷爲”佳”。當 移除一或多個方塊時,該組合物之膠黏性評斷爲”差”。"4-—Η BA" manufactured by Industry Co., Ltd.) Component (D) D1: 2,2-dimethoxy-1,2-diphenylethylene-1_one (Ciba Specialty Chemicals Co., Ltd. Manufactured by "Irgacure 651") D2 printed by the Consumer Cooperative of Intellectual Property Bureau of the Ministry of Economic Affairs: 2-Hydroxy-2-methyl-1 monophenyl-propan-1-one (Ciba Specialty Chemicals Co., Ltd. “Darcur 1173”) Component (E) E 1: r —Hydroxythiopropyltrimethoxy stone wicker house (Toray-Dow Corning 3 Hill (: 〇1 ^ 0〇., 1 ^ (1.Manufactured by "3116062" ”) -29- This paper size applies to Chinese National Standard (CNS) A4 (210 X 297 mm) 574339 A7 B7 V. Description of the invention (27) Other documents (Please read the notes on the back before filling this page) Ethylene oxide addition of bisphenol A di (meth) acrylate ("VR — 7 7" manufactured by Showa Highpolymer Co., Ltd.) Glycol diacrylate (light acrylic acid manufactured by Kyoeosha Chemical Co., Ltd.) Esters 4 EGA ") Phenoxyethyl acrylate (" NewFrontierPHE "manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) 2 -Methyl-1— [4- (methylthio) phenyl] -2—morpholinyl—propan-1-one ("Irgacure 907" manufactured by Ciba Specialty Chemicals Co., Ltd.) 2,2_sulfur Ethylene bis [3- (3,5-di-third-butyl-4-hydroxyphenyl) propionate] ("Irganox 1035" manufactured by Ciba Specialty Chemicals Co., Ltd.) Edge curability, Moisture and heat resistance, and the adhesiveness to the substrate of the prepared composition (compositions of Examples 1 to 9) were measured and evaluated as described below. Printed by the Consumer Cooperative of Intellectual Property Bureau, Ministry of Economic Affairs- 30- 574339 A7 B7 V. Description of the invention (28) (Please read the precautions on the back before filling this page) When adhesive, the edge curability of the composition is judged as "good". The irradiation dose is 2 5 0 When there is no adhesiveness after millijoules / cm2, the edge curability of the compound is judged as "excellent". {21 Moisture and heat resistance Use the method described in item (1) above at 500 millijoules / The composition was irradiated at cm 2 to make the substrate adhere. After being placed in an isothermal humidifier at a temperature of 90 ° C and a relative humidity of 98% RH, abnormalities such as foaming or corrosion were found on the adhesive layer or the interface between the adhesive and the substrate At this time, the composition was judged to be "poor" in damp heat resistance. If no abnormality was found, the composition was judged to be "good" in damp heat resistance. ill Relative to an adhesive part of a material Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs This composition is applied to an aluminum or gold film evaporated on a PC substrate using a sputtering method. The composition was irradiated with a dose of 1000 mJ / cm2 in a nitrogen atmosphere to obtain a composition cured film having a thickness of 50 microns. The cured film was subjected to a cross-cut cellophane tape peel test. When the aluminum film or gold film was not removed from the PC substrate, the adhesiveness of the composition was judged as "good". When one or more squares were removed, the composition was evaluated as "poor".

表1顯示接合藉濺鍍p c基材所製備之p C基材及鋁 基材的結果,及接合藉濺鑛p C基材所製備之P C基材及 黃金基材的結果。實施例7之組合物——不含組份(B ) 具有相對差之邊緣固化性,但具有良好之耐濕熱性。 實施例8及9之組合物——非組合含有組份(C )及(D -31 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 574339 A7 B7 五、發明説明(29) ),具有相對較差之耐濕熱性,但具有良好之邊緣固化性 。實施例6之組合物--不含組份(E ) - -對於黃金具 性 黏 膠 之 差 較 對 相 有 (請先閲讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 -32- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 A7 B7 五、發明説明(30) 經濟部智慧財產局員工消費合作社印製 £ 實施例 σ\ 〇 CSI CN un r-H CO _ 酬 〇〇 〇 ν〇 CO CN1 m· CO c〇 t _丨_ < CO 〇 CNI UO CN1 cn CO τ—Η CO v〇 CN UO CN| VO CO CO < < CO S 〇 Csl 寸 τ—Η CO 寸 CO CN| Η CO fl CO 〇 〇 CO cn r Ή CO ο CSI 〇 l£l CN1 CO CO cn 〇 CN1 cn CO !' < cn Τ-Η Τ—Η 氧化乙烯加成雙酚A二(甲基)丙烯酸酯 (重量份數) 乙二醇二丙烯酸酯 丙烯酸苯氧乙酯 s CNI r—H Q s 2-甲基-l-[4-(甲硫基)苯基]-2-嗎啉-丙-1-酮 卜 HI 城 1 11 CO ώ U 55 命邐 l\] 1I77 *民 π橄 3¾ PC基材與鋁基材之組合物 邊緣固化性 耐濕熱性 黃金基材與鋁基材之組合物 邊緣固化性 耐濕熱性 (請先閲讀背面之注意事項再填寫本頁) ;裝· 訂 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -33-Table 1 shows the results of joining the PC substrate and the aluminum substrate prepared by sputtering the PC substrate and the results of joining the PC substrate and the gold substrate prepared by sputtering the PC substrate. The composition of Example 7-without component (B), has relatively poor edge-curing properties, but has good moist-heat resistance. Compositions of Examples 8 and 9-non-combination containing components (C) and (D -31-this paper size applies Chinese National Standard (CNS) A4 specifications (210X 297 mm) 574339 A7 B7 V. Description of the invention ( 29)), has relatively poor heat and humidity resistance, but has good edge curing. The composition of Example 6-does not contain component (E)--the difference between gold viscose is relatively different (please read the precautions on the back before filling out this page) Employee Cooperative of Intellectual Property Bureau of the Ministry of Economic Affairs Printing-32- This paper size is in accordance with Chinese National Standard (CNS) A4 (210X297 mm) 574339 A7 B7 V. Description of Invention (30) Printed by the Consumer Cooperative of Intellectual Property Bureau of the Ministry of Economic Affairs £ Example σ \ 〇CSI CN un rH CO _ Complement 〇〇〇〇ν〇CO CN1 m · CO c〇t _ 丨 _ < CO 〇CNI UO CN1 cn CO τ—Η CO v〇CN UO CN | VO CO CO < < CO S 〇 Csl inch τ—Η CO inch CO CN | Η CO fl CO 〇〇CO cn r Ή CO ο CSI 〇l £ l CN1 CO CO cn 〇CN1 cn CO! '≪ cn Τ-Η Τ—Η ethylene oxide addition Bisphenol A di (meth) acrylate (parts by weight) ethylene glycol diacrylate phenoxyethyl acrylate CNI r—HQ s 2-methyl-l- [4- (methylthio) phenyl] -2-morpholine-propan-1-one BU HI City 1 1 1 CO trophy U 55 命 逦 l] 1I77 * 民 π olive 3¾ PC substrate and aluminum substrate composition edge curing moist heat resistance Gold substrate and aluminum substrate composition edge curing moist heat resistance (please (Please read the notes on the back before filling this page); The size of the binding and binding paper is applicable to China National Standard (CNS) A4 (210X297 mm) -33-

Claims (1)

574339574339 A8 B8 C8 D8 修正替換本 日 六、申請專利範圍 附件2: 第90 1 1 9903號專利申請案 、 中文申請專利範圍無劃線替換本 民國92年4月17日修正 1 . 一種組合物,其包含: (a) 20 — 80重量%的輻射可固化之寡聚物;及 (b) 〇 · 05 - 5重量%的二烷基胺基苯甲酸酯, 相對於組合物總重,其中該輻射可 元醇化合物、多異氰酸酯化合物 丙烯酸酯化合物進行反應所製得。 2 .如申請專利範圍第1項之組合物,另包含(甲基 )丙烯酸羥烷酯。 3 ·如申請專利範圍第2項之組合物,其中該組合物 係包含相對於該組合物之總重爲 甲基)丙烯酸羥烷酯。 4 .如申請專利範圍第1項之 固化之寡聚物係藉著多 及含有羥基之(甲基) 一 7 0重量百分比之 (請先閱讀背面之注意事項再填寫本頁) 訂 經濟部智慧財產局員二消费合作让卬製 組合物,其進一步包含 2 —二苯基乙—1-.酮 2 —羥基一 2 -甲基—1 —苯基丙一 1 一酮、及1 一羥 選自包括2,2 -二甲氧基 基環己基苯基酮之群的化合物。 5 _如申請專利範圍第2項之組合物,其進一步包含 選自包括2,2 -二甲氧基—1 ,2 —二苯基乙—1—酮 、2 -經基—2 —甲基—1 —苯基丙—1 一酮 '及1 一經 基環己基苯基酮之群的化合物。 .一種組合物,其包含 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 574339 經濟部智慧財產局員工消費合作社印製 A8 B8 C8 D8 六、申請專利範圍 (a) 20-80重量%的輻射可固化之寡聚物; (b) 〇 . 〇5 — 5重量%的二烷基胺基苯甲酸酯; (c) 5 — 7 0重量%的(甲基)丙烯酸羥基烷酯, 及 (d) 〇 . 01-15重量%的至少一種選自2,2 一二甲氧基一 1 ,2 —二苯基乙—1—酮、2 —羥基一2 一甲基一 1 —苯基丙一 1 一酮、及1 —羥基環己基苯基酮 之群的化合物,相對於組合物總重,其中該輻射可固化之 寡聚物係藉著多元醇化合物、多異氰酸酯化合物、及含有 羥基之(甲基)丙烯酸酯化合物進行反應所製得。 7 .如申請專利範圍第1或6項之組合物,其中該組 合物係包含對-二甲基胺基苯甲酸乙酯。 8 _如申請專利範圍第1或6項之組合物,其係進一 步包含 (e )具有甲氧甲矽烷基之硫醇化合物。 9 ·如申請專利範圍第8項之組合物,其中該組合物 係包含相對於該組合物總重爲0 · 1 - 5重量百分比之.該 硫醇化合物。 1 〇 ·如申請專利範圍第1或6項之組合物,其中該 多元醇化合物係具有2 5 0 - 8 0 0之數量平均分子量。 1 1 ·如申請專利範圍第1或6項之組合物,其中該 組合物係包含(甲基)丙烯酸羥基C : 一 C 6烷酯。 1 2 ·如申請專利範圍第1或6項之組合物,其中該 組合物係包含(甲基)丙烯酸4 -羥基丁酯。 (請先閱讀背面之注意事項再填寫本頁)A8 B8 C8 D8 Amendment and Replacement Today 6. Attachment to Patent Scope Annex 2: Patent Application No. 90 1 1 9903, Chinese Application for Patent Scope Unlined Replacement Amendment 1. April 17, 1992 Amendment 1. A composition comprising : (A) 20-80% by weight of a radiation-curable oligomer; and (b) 0.05-5% by weight of a dialkylaminobenzoate relative to the total weight of the composition, wherein the radiation It can be obtained by reacting an alcohol compound and a polyisocyanate compound with an acrylate compound. 2. The composition according to item 1 of the patent application scope, further comprising a hydroxyalkyl (meth) acrylate. 3. The composition according to item 2 of the patent application range, wherein the composition comprises hydroxyalkyl methacrylate relative to the total weight of the composition. 4. If the solidified oligomer in item 1 of the scope of patent application is based on polymethylated and (hydroxy) -containing (methyl)-70% by weight (please read the precautions on the back before filling this page). A member of the property bureau, a consumer cooperative composition, further comprises 2-diphenylethyl-1-.one, 2-hydroxy-1, 2-methyl-1, phenylpropanyl, 1-ketone, and 1-hydroxyl selected from Compounds including the group of 2,2-dimethoxycyclohexylphenyl ketones. 5 _ The composition according to item 2 of the scope of patent application, further comprising a member selected from the group consisting of 2,2-dimethoxy-1, 2-diphenylethyl-1-one, 2-meryl-2-methyl —1 —Phenylpropanone-1 ketone 'and 1-Cyclohexylphenyl ketone compounds. A composition containing the paper size applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 574339 Printed by the Consumers' Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs A8 B8 C8 D8 6. Scope of patent application (a) 20-80 Radiation curable oligomers by weight; (b) 0.05 to 5% by weight of dialkylaminobenzoate; (c) 5 to 70% by weight of (meth) acrylic hydroxyalkane Ester, and (d) at least one of 0.01-15% by weight selected from the group consisting of 2,2-dimethoxy-1,2-diphenylethyl-1-one, 2-hydroxy-2, methyl-1 The compounds of the group of —phenylpropanone monoone and 1 —hydroxycyclohexylphenyl ketone relative to the total weight of the composition, wherein the radiation-curable oligomer is made of a polyol compound, polyisocyanate compound, And a hydroxyl group-containing (meth) acrylate compound. 7. The composition according to claim 1 or 6, wherein the composition comprises ethyl p-dimethylaminobenzoate. 8 _ The composition according to item 1 or 6 of the scope of patent application, which further comprises (e) a thiol compound having a methoxysilyl group. 9. The composition according to item 8 of the scope of patent application, wherein the composition comprises the mercaptan compound in an amount of 0. 1 to 5 weight percent relative to the total weight of the composition. 1 0. The composition according to item 1 or 6 of the scope of patent application, wherein the polyhydric alcohol compound has a number average molecular weight of 250 to 800. 1 1 · The composition according to item 1 or 6 of the scope of patent application, wherein the composition comprises a hydroxy C: -C 6 alkyl (meth) acrylate. 1 2 The composition according to item 1 or 6 of the scope of patent application, wherein the composition comprises 4-hydroxybutyl (meth) acrylate. (Please read the notes on the back before filling this page) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -2 _ 574339 A8 B8 C8 D8 六、申請專利範圍 1 3 .如申請專利範圍第1或6項之組合物·,其中該 組合物係包含2,2 -二甲氧基一 1 ,2 -二苯基乙一 1 —酮及2 -羥基—2 —甲基—1 —苯基丙—1 —酮。 1 4 ·如申請專利範圍第1或6項之組合物,其中該 固化組合物之6 0微米厚層在6 0 0 - 7 0 0奈米下係具 有9 0百分比或更高之透光度。 1 5 ·如申請專利範圍第1或6項之組合物,其中該 組合物係具有150-2, OOOmPa·s之黏度。 1 6 ·如申請專利範圍第1或6項之組合物,其中該 組合物係作爲供光碟使用之膠黏劑。 1 7 .如申請專利範圍第1 6項之組合物,其中該光 碟係爲數位式多用途磁碟。 1 8 · —種包含膠黏劑之光碟,該膠黏劑係藉著使如 申請專利範圍第1或6項之組合物進行固化所製得。 1 9 ·如申請專利範圍第1 8項之光碟,其中該光碟 係爲數位式多用途磁碟。 -- (請先聞讀背面之注意事項再填寫本頁) 、言 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)This paper size applies to China National Standard (CNS) A4 specification (210X297 mm) -2 _ 574339 A8 B8 C8 D8 VI. Application for patent scope 1 3. For the composition of patent application scope 1 or item 6, where the combination The system contains 2,2-dimethoxy-1,2-diphenylethyl-1-one and 2-hydroxy-2-methyl-1-phenylpropan-1-one. 1 4 · The composition according to item 1 or 6 of the scope of patent application, wherein the 60 micron thick layer of the cured composition has a light transmittance of 90 percent or more at 600 to 700 nanometers. . 15 · The composition according to item 1 or 6 of the scope of patent application, wherein the composition has a viscosity of 150-2,000 mPa · s. 16 · The composition according to item 1 or 6 of the patent application scope, wherein the composition is used as an adhesive for optical discs. 17. The composition according to item 16 of the scope of patent application, wherein the optical disc is a digital versatile disk. 1 8 · An optical disc containing an adhesive, which is prepared by curing a composition such as those in the scope of claims 1 or 6 of the patent application. 19 · The optical disc of item 18 in the scope of patent application, wherein the optical disc is a digital versatile disk. -(Please read the precautions on the back before filling out this page), and printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs This paper size applies to China National Standard (CNS) A4 (210X297 mm)
TW90119903A 2000-08-15 2001-08-14 Adhesive composition for optical disks TW574339B (en)

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