JP2707458B2 - Acrylic syrup composition - Google Patents
Acrylic syrup compositionInfo
- Publication number
- JP2707458B2 JP2707458B2 JP30760088A JP30760088A JP2707458B2 JP 2707458 B2 JP2707458 B2 JP 2707458B2 JP 30760088 A JP30760088 A JP 30760088A JP 30760088 A JP30760088 A JP 30760088A JP 2707458 B2 JP2707458 B2 JP 2707458B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- acrylic syrup
- acrylic
- resin
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims description 47
- 239000006188 syrup Substances 0.000 title claims description 44
- 235000020357 syrup Nutrition 0.000 title claims description 44
- 239000000203 mixture Substances 0.000 title claims description 17
- 239000000178 monomer Substances 0.000 claims description 31
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 22
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 15
- 239000004925 Acrylic resin Substances 0.000 claims description 11
- 229920000178 Acrylic resin Polymers 0.000 claims description 9
- 229920001567 vinyl ester resin Polymers 0.000 claims description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 11
- 238000009835 boiling Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 8
- 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 6
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 6
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 239000003505 polymerization initiator Substances 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- HTWRFCRQSLVESJ-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCOC(=O)C(C)=C HTWRFCRQSLVESJ-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-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
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- ULQMPOIOSDXIGC-UHFFFAOYSA-N [2,2-dimethyl-3-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)COC(=O)C(C)=C ULQMPOIOSDXIGC-UHFFFAOYSA-N 0.000 description 1
- JUDXBRVLWDGRBC-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(COC(=O)C(C)=C)COC(=O)C(C)=C JUDXBRVLWDGRBC-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- SWHLOXLFJPTYTL-UHFFFAOYSA-N [2-methyl-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(COC(=O)C(C)=C)COC(=O)C(C)=C SWHLOXLFJPTYTL-UHFFFAOYSA-N 0.000 description 1
- HSZUHSXXAOWGQY-UHFFFAOYSA-N [2-methyl-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(C)(COC(=O)C=C)COC(=O)C=C HSZUHSXXAOWGQY-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005651 polypropylene glycol dimethacrylate Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、透明性、低収縮性及び耐煮沸性等に優れた
成形用のアクリルシロップ組成物に関するものである。The present invention relates to a molding acrylic syrup composition having excellent transparency, low shrinkage, boiling resistance and the like.
メタクリル酸メチルを主成分とするアクリルシロップ
組成物は、透明性、耐候性に優れていることからガラス
繊維強化板、キッチンカウンター台、洗面台等に使用さ
れている。また、最近ではポリエステルに変わる建築材
料としての期待も大きくなってきており、耐煮沸性、耐
熱性および耐衝撃性等の改善が望まれている。BACKGROUND ART An acrylic syrup composition containing methyl methacrylate as a main component is used for a glass fiber reinforced plate, a kitchen countertop, a wash basin, and the like because of its excellent transparency and weather resistance. Further, recently, there is a growing expectation as a building material replacing polyester, and improvements in boiling resistance, heat resistance, impact resistance and the like are desired.
一般に、メタクリル系樹脂の耐熱性を向上させる方法
としては、α−メチルスチレンを共重合させる方法(US
P 3,135,723)、無水マレイン酸を共重合させる方法
(特公昭45−31953号,特公昭49−10156号)、メチルメ
タクリレート、α−メチルスチレン及びマレイミドを共
重合させる方法(特開昭48−95490号)等数多くの方法
が挙げられる。Generally, as a method for improving the heat resistance of a methacrylic resin, a method of copolymerizing α-methylstyrene (US Pat.
P. 3,135,723), a method of copolymerizing maleic anhydride (JP-B-45-31953, JP-B-49-10156), a method of copolymerizing methyl methacrylate, α-methylstyrene and maleimide (JP-A-48-95490). ) And many other methods.
しかし、これらの方法はいずれも耐熱性は向上するも
のの、重合速度が著しく遅かったり、重合物の透明性、
耐候性および耐煮沸性が低下するなどの欠点がある。However, although the heat resistance of each of these methods is improved, the polymerization rate is extremely slow, the transparency of the polymer,
There are drawbacks such as a decrease in weather resistance and boiling resistance.
さらに、これらの重合方法をアクリルシロップに用い
る場合、アクリルシロップ中に残存する架橋性不飽和単
量体等の影響による、成形時の反応の遅さから効率良く
成形物を得られず、実用化するには問題が多い。Furthermore, when these polymerization methods are used for acrylic syrup, a molded product cannot be obtained efficiently due to the slow reaction during molding due to the influence of cross-linkable unsaturated monomers remaining in the acrylic syrup, and practical use is not possible. There are many problems to do.
アクリルシロップの物性の中で、特に耐煮沸性、耐熱
性を改善する方法として、グリコールジアクリレートま
たはジメタクリレートのような架橋性不飽和単量体を共
重合させることは有効な手段であるが、アクリルシロッ
プを成形可能なものにするためには、粘度を一定範囲内
に保たなければならない。Among the physical properties of acrylic syrup, especially as a method for improving boiling resistance and heat resistance, it is effective means to copolymerize a crosslinkable unsaturated monomer such as glycol diacrylate or dimethacrylate, In order to make the acrylic syrup moldable, the viscosity must be kept within a certain range.
その結果、アクリルシロップ中における樹脂分が少な
くなり、後重合し成形する時、成形物に割れ、ひけ(成
形時の部分的な波形の凹部のこと)等を生じてしまう。
また、粘度を成形可能なものに保ちながら樹脂分を多く
しようとすると分子量の低下を生じ、耐煮沸性、耐熱
性、強度および耐衝撃性が極端に低下してしまうという
欠点を有している。As a result, the resin content in the acrylic syrup is reduced, and the molded product cracks or sinks (a partially corrugated concave portion during molding) during post-polymerization and molding.
In addition, there is a drawback that if an attempt is made to increase the resin content while keeping the viscosity at a level capable of being molded, the molecular weight is reduced, and boiling resistance, heat resistance, strength and impact resistance are extremely reduced. .
そこで、本発明は、特に収縮率を小さくし、成形性を
改善し、さらに透明性を維持した耐煮沸性に優れたアク
リルシロップ組成物を提供することを課題とする。Therefore, an object of the present invention is to provide an acrylic syrup composition having a reduced shrinkage, improved moldability, and excellent transparency while maintaining transparency.
本発明者らは、前記課題を解決するために鋭意検討し
た結果、メタクリル酸メチルを主成分とするエチレン性
不飽和単量体と架橋性不飽和単量体からなる高度に架橋
させたアクリルシロップにラジカル重合可能な樹脂中に
二重結合をもった樹脂をブレンドすることで本発明の目
的が達成されることを見出し、本発明を完成させるに至
った。The present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, a highly crosslinked acrylic syrup composed of an ethylenically unsaturated monomer containing methyl methacrylate as a main component and a crosslinkable unsaturated monomer. It has been found that the object of the present invention can be achieved by blending a resin having a double bond in a radically polymerizable resin, thereby completing the present invention.
すなわち、本発明は次のA成分80〜20重量%とB成分
20〜80重量%からなるアクリルシロップ組成物に関する
ものである。That is, the present invention relates to the following 80 to 20% by weight of component A and component B
The present invention relates to an acrylic syrup composition comprising 20 to 80% by weight.
(a)A成分:メタクリル酸メチルを主成分とするエチ
レン性不飽和単量体の総モル数1に対し、架橋性不飽和
単量体を0.002〜0.03モル加え、共重合させて得られる
アクリルシロップのうち、重量平均分子量(MW)が2000
00〜800000、数平均分子量(MN)が20000〜100000で、
その比(MW/MN)が2〜40であるところの高架橋アクリ
ルシロップ。(A) Component A: Acrylic obtained by adding 0.002 to 0.03 mol of a crosslinkable unsaturated monomer to the total number of moles of ethylenically unsaturated monomer having methyl methacrylate as a main component, and copolymerizing the same. Syrup has a weight average molecular weight (MW) of 2000
00 to 800,000, number average molecular weight (MN) is 2000 to 100,000,
Highly crosslinked acrylic syrup whose ratio (MW / MN) is 2 to 40.
(b)B成分:エチレン性不飽和単量体を含有し、樹脂
中に少なくとも2つ以上のエチレン性不飽和基を有す
る、ビニルエステル樹脂またはアクリル樹脂を50〜90重
量%含有するアクリルシロップ。(B) Component B: an acrylic syrup containing an ethylenically unsaturated monomer and having 50 to 90% by weight of a vinyl ester resin or an acrylic resin having at least two or more ethylenically unsaturated groups in the resin.
本発明は、メタクリル酸メチルを主成分とするエチレ
ン性不飽和単量体と架橋性不飽和単量体を共重合させて
得られるアクリルシロップのうち、特に架橋密度を上げ
た高架橋アクリルシロップにビニルエステル樹脂または
アクリル樹脂を加えてなる透明性を維持した低収縮性・
耐煮沸性等に優れた成形用のアクリルシロップ組成物で
ある。The present invention is an acrylic syrup obtained by copolymerizing an ethylenically unsaturated monomer containing methyl methacrylate as a main component and a crosslinkable unsaturated monomer. Low shrinkage with transparency maintained by adding ester resin or acrylic resin
It is an acrylic syrup composition for molding excellent in boiling resistance and the like.
以下、本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail.
先ず、メタクリル酸メチルを主成分とするエチレン性
不飽和単量体の総モル数1に対し、架橋性不飽和単量体
を0.002〜0.03モル、好ましくは0.01〜0.02モル加え共
重合させて樹脂分10〜50重量%の高度に架橋したアクリ
ルシロップ(A)を得る。First, a crosslinkable unsaturated monomer is added in an amount of 0.002 to 0.03 mol, preferably 0.01 to 0.02 mol, based on the total number of moles of the ethylenically unsaturated monomer having methyl methacrylate as a main component of 1, and copolymerized. A highly crosslinked acrylic syrup (A) of 10 to 50% by weight is obtained.
この高架橋アクリルシロップ(A)の製法は、特に限
定しないが、アゾビス系、有機過酸化物系等の重合開始
剤を上記単量体の混合液中に加え、また必要に応じてn
−ドデシルメルカプタン、チオグリコール酸等の分子量
調整剤を加え、60〜120℃の間で加熱重合させ重合液の
粘度が2〜6poiseのところで重合禁止剤を加え冷却し、
目的とする高架橋アクリルシロップ(A)を得る。The method for producing the highly crosslinked acrylic syrup (A) is not particularly limited, but an azobis-based or organic peroxide-based polymerization initiator is added to a mixture of the above monomers, and if necessary, n
-Add a molecular weight modifier such as dodecyl mercaptan, thioglycolic acid, heat polymerization between 60 and 120 ° C, add a polymerization inhibitor when the viscosity of the polymerization solution is 2 to 6 poise, and cool.
The desired highly crosslinked acrylic syrup (A) is obtained.
この高架橋アクリルシロップ(A)は、重量平均分子
量(MW)が200000〜800000、数平均分子量(MN)が2000
0〜100000、その比(MW/MN)が2〜40、好ましくは5〜
30であるところのものが望ましい。This highly crosslinked acrylic syrup (A) has a weight average molecular weight (MW) of 200,000 to 800,000 and a number average molecular weight (MN) of 2,000.
0 to 100,000, the ratio (MW / MN) is 2 to 40, preferably 5 to
A value of 30 is desirable.
主成分として用いられるメタクリル酸メチルの使用量
は、エチレン性不飽和単量体の総モル数1のうち0.5〜
1.0モル、好ましくは0.7〜1.0モルである。最終成形物
の硬度、耐熱性および耐候性を考慮するとメタクリル酸
メチルが0.5モル未満では好ましくない。The amount of methyl methacrylate used as the main component is 0.5 to 1 in the total number of moles 1 of the ethylenically unsaturated monomer.
1.0 mole, preferably 0.7 to 1.0 mole. In consideration of the hardness, heat resistance and weather resistance of the final molded product, it is not preferable that the content of methyl methacrylate is less than 0.5 mol.
主成分として用いられるメタクリル酸メチル以外のエ
チレン性不飽和単量体としては、例えばメタクリル酸エ
チル、メタクリル酸ブチル、メタクリル酸イソブチル、
メタクリル酸2−エチルヘキシル、メタクリル酸ラウリ
ル、メタクリル酸プロピル、メタクリル酸イソプロピ
ル、メタクリル酸2−ヒドロキシエチル、メタクリル酸
2−ヒドロキシプロピル、メタクリル酸3−ヒドロキシ
プロピル、メタクリル酸等のメタクリル酸及びそのエス
テル類、アクリル酸メチル、アクリル酸エチル、アクリ
ル酸ブチル、アクリル酸プロピル、アクリル酸イソプロ
ピル、アクリル酸2−エチルヘキシル、アクリル酸ラウ
リル、アクリル酸2−ヒドロキシエチル、アクリル酸等
のアクリル酸及びそのエステル類、その他、酢酸ビニ
ル、アクリロニトリル、アクリルアミド、メタクリルア
ミド、スチレン、α−メチルスチレン、無水マレイン酸
等がある。Examples of ethylenically unsaturated monomers other than methyl methacrylate used as the main component include, for example, ethyl methacrylate, butyl methacrylate, isobutyl methacrylate,
Methacrylic acid and its esters such as 2-ethylhexyl methacrylate, lauryl methacrylate, propyl methacrylate, isopropyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 3-hydroxypropyl methacrylate, methacrylic acid, Acrylic acid and its esters such as methyl acrylate, ethyl acrylate, butyl acrylate, propyl acrylate, isopropyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate, 2-hydroxyethyl acrylate, acrylic acid, etc., Examples include vinyl acetate, acrylonitrile, acrylamide, methacrylamide, styrene, α-methylstyrene, and maleic anhydride.
また、架橋性不飽和単量体としては、例えば、エチレ
ングリコールジメタクリレート、ジエチレングリコール
ジメタクリレート、トリエチレングリコールジメタクリ
レート、ポリエチレングリコールジメタクリレート、1,
3−ブチレングリコールジメタクリレート、1,3−プロピ
レングリコールジメタクリレート、1,4−ブチレングリ
コールジメタクリレート、ポリプロピレングリコールジ
メタクリレート、1,6−ヘキサンジオールジメタクリレ
ート、ネオペンチルグリコールジメタクリレート、トリ
メチロールプロパントリアクリレート、トリメチロール
プロパントリメタクリレート、トリメチロールエタント
リアクリレート、トリメチロールエタントリメタクリレ
ート、テトラメチロールメタントリアクリレート、テト
ラメチロールメタントリメタクリレート、テトラメチロ
ールメタンテトラアクリレート等が挙げられるが、この
架橋性アクリルシロップを得るためには、特にポリエチ
レングリコールジメタクリレートが望ましい。Examples of the crosslinking unsaturated monomer include, for example, ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, polyethylene glycol dimethacrylate,
3-butylene glycol dimethacrylate, 1,3-propylene glycol dimethacrylate, 1,4-butylene glycol dimethacrylate, polypropylene glycol dimethacrylate, 1,6-hexanediol dimethacrylate, neopentyl glycol dimethacrylate, trimethylolpropane triacrylate , Trimethylolpropane trimethacrylate, trimethylolethane triacrylate, trimethylolethane trimethacrylate, tetramethylolmethane triacrylate, tetramethylolmethanetrimethacrylate, tetramethylolmethanetetraacrylate, and the like.In order to obtain this crosslinkable acrylic syrup In particular, polyethylene glycol dimethacrylate is desirable.
架橋性不飽和単量体の添加量は、エチレン性不飽和単
量体の総モル数1に対して、0.002〜0.03モルである。
ただし、架橋性不飽和単量体は、分子量の幅も広く、一
分子中の二重結合の数も異なるものが多く存在するた
め、これらの添加量は一分子中に含まれる二重結合の数
(n)によって規定することが望ましい。The amount of the crosslinkable unsaturated monomer to be added is 0.002 to 0.03 mol per 1 mol of the total number of ethylenically unsaturated monomers.
However, crosslinkable unsaturated monomers have a wide range of molecular weights and many have different numbers of double bonds in one molecule.Therefore, the amount of these added is the amount of double bonds contained in one molecule. It is desirable to define by the number (n).
一般式で表すと一分子中に二つ以上の二重結合を有す
る架橋性不飽和単量体の添加量は、0.01/n〜0.06/nモル
である。When represented by the general formula, the amount of the crosslinkable unsaturated monomer having two or more double bonds in one molecule is 0.01 / n to 0.06 / n mol.
本発明で使用する架橋性不飽和単量体は、一分子中に
二重結合を2〜4個有する場合、すなわち、n=2〜4
の場合である。The crosslinkable unsaturated monomer used in the present invention has 2 to 4 double bonds in one molecule, that is, n = 2 to 4
Is the case.
n=2の場合、その使用量は、0.005〜0.03モル、n
=3の場合、その使用量は、0.0034〜0.02モル、n=4
の場合、その使用量は、0.0025〜0.015モルである。When n = 2, the amount used is 0.005 to 0.03 mol, n
= 3, the amount used is 0.0034-0.02 mol, n = 4
In this case, the amount used is 0.0025 to 0.015 mol.
この架橋性不飽和単量体の添加量が、0.002モル未満
の場合は、アクリルシロップの架橋密度が小さすぎ、本
発明の目的とする高架橋アクリルシロップは得られな
い。また、0.03モルを越える場合は、共重合時に温度制
御がしにくく、暴走し易く、仮に共重合させたとして
も、その重合度が小さすぎて成形材料として好ましくな
い。When the amount of the crosslinkable unsaturated monomer is less than 0.002 mol, the crosslink density of the acrylic syrup is too small, and the highly crosslinked acrylic syrup intended for the present invention cannot be obtained. On the other hand, if it exceeds 0.03 mol, it is difficult to control the temperature at the time of copolymerization, runaway easily, and even if copolymerized, the degree of polymerization is too small, which is not preferable as a molding material.
次に加えるビニルエステル樹脂およびアクリル樹脂に
ついて、 ビニルエステル樹脂としては、ビスフェノール系エポ
キシアクリレート樹脂、ノボラック系エポキシアクリレ
ート樹脂、イソフタル酸系ビニル変性不飽和ポリエステ
ル樹脂等が挙げられる。Next, regarding the vinyl ester resin and the acrylic resin to be added, examples of the vinyl ester resin include a bisphenol-based epoxy acrylate resin, a novolak-based epoxy acrylate resin, and an isophthalic acid-based vinyl-modified unsaturated polyester resin.
これらのビニルエステル樹脂は50〜90重量%含有さ
れ、その粘度が3〜100poiseであるところのアクリルシ
ロップとして用いられる。These vinyl ester resins are used as an acrylic syrup containing 50 to 90% by weight and having a viscosity of 3 to 100 poise.
一方、アクリル樹脂については、例えば、特開昭61−
19601号中に示されるような方法で、アクリル樹脂中に
グリシジル基含有単量体を共重合させておき、グリシジ
ル基を2個以上有する共重合体とし、これをグリシジル
基との反応性を有する単量体を含むエチレン性不飽和単
量体中に50〜90重量%含有させ、樹脂中のグリシジル基
の1〜100%を前記エチレン性不飽和単量体と反応せし
めた2個以上のエチレン性不飽和基を有する樹脂を含有
する、粘度3〜100poiseであるアクリルシロップ又はア
クリル樹脂中にグリシジル基と反応性を有するエチレン
性不飽和単量体を共重合させておき、これにグリシジル
基含有エチレン性不飽和単量体を1〜100%反応せしめ
た2つ以上のエチレン性不飽和基を有する樹脂を含有す
る、粘度3〜100poiseのアクリルシロップとして用いら
れる。このようなB成分のアクリルシロップとしては、
市販のアクリル樹脂SM−100B−4、SM−100B−3(いず
れも、三井東圧化学(株)製、商品名)がある。On the other hand, for acrylic resin, for example,
By a method as shown in 19601, a glycidyl group-containing monomer is copolymerized in an acrylic resin to obtain a copolymer having two or more glycidyl groups, which has reactivity with a glycidyl group. Two or more ethylenes containing 50 to 90% by weight of an ethylenically unsaturated monomer containing a monomer and reacting 1 to 100% of glycidyl groups in the resin with the ethylenically unsaturated monomer; An ethylenically unsaturated monomer having a reactivity with a glycidyl group is copolymerized in an acrylic syrup or an acrylic resin having a viscosity of 3 to 100 poise containing a resin having a glycidyl group. It is used as an acrylic syrup having a viscosity of 3 to 100 poise containing a resin having two or more ethylenically unsaturated groups obtained by reacting 1 to 100% of an ethylenically unsaturated monomer. As such an acrylic syrup of the component B,
There are commercially available acrylic resins SM-100B-4 and SM-100B-3 (both manufactured by Mitsui Toatsu Chemicals, Inc., trade names).
これらのアクリルシロップを前記した高架橋アクリル
シロップ(A成分)に混合し、合計量として100重量%
とする。These acrylic syrups are mixed with the above-mentioned highly crosslinked acrylic syrup (component A), and the total amount is 100% by weight.
And
混合したアクリルシロップに含まれる架橋性不飽和単
量体の量は、A成分とB成分を混合した状態で混合液中
に含まれる量が1〜30重量%であり、好ましくは3〜20
重量%である。1重量%未満では、耐煮沸性が不十分と
なり、30重量%を越えると、本来目的としている低収縮
性の効果が損なわれるおそれがあり好ましくない。The amount of the crosslinkable unsaturated monomer contained in the mixed acrylic syrup is 1 to 30% by weight, preferably 3 to 20% by weight in the mixed solution in which the component A and the component B are mixed.
% By weight. If it is less than 1% by weight, the boiling resistance becomes insufficient, and if it exceeds 30% by weight, the originally intended effect of low shrinkage may be impaired, which is not preferred.
A成分とB成分の混合量は、用いる高架橋アクリルシ
ロップおよびアクリルシロップそれぞれに含まれる樹脂
分によるが、A成分/B成分=20/80〜80/20が望ましい。The mixing amount of the component A and the component B depends on the resin content contained in each of the highly crosslinked acrylic syrup and the acrylic syrup to be used, but it is desirable that the component A / B component = 20/80 to 80/20.
一般に低収縮化剤として異種樹脂を混合すると透明性
が低下し、白濁する傾向があるが、本発明で得られるA
成分を用いると透明性は損なわれない。In general, when a different resin is mixed as a low-shrinkage agent, transparency tends to decrease, and the mixture tends to be cloudy.
Use of the components does not impair transparency.
また、本発明によって得られるA成分は、単独での攪
拌混合が困難となる傾向があるが、B成分を混合すると
容易に攪拌混合ができる。特に無機充填剤を用いると通
常のアクリルシロップに比べて増粘しにくく充填剤の高
充填が可能となる。本発明で得られたアクリルシロップ
組成物は、必要に応じて無機フィラー、その他の充填
剤、顔料、染料等の着色剤、重合開始剤、重合促進剤等
の添加剤を配合し、金型、樹脂型、ガラス型等の型枠に
注入し、加圧または常圧下、加熱もしくは室温にて硬化
させ、大理石調の成形品を得ることができる。The component A obtained by the present invention tends to be difficult to stir and mix alone, but when the component B is mixed, stirring and mixing can be easily performed. In particular, when an inorganic filler is used, it is difficult to increase the viscosity as compared with ordinary acrylic syrup, and the filler can be filled at a high level. The acrylic syrup composition obtained in the present invention is blended with additives such as inorganic fillers, other fillers, pigments, coloring agents such as dyes, polymerization initiators, polymerization accelerators, if necessary, a mold, It is poured into a mold such as a resin mold or a glass mold and cured under heating or room temperature under pressure or normal pressure to obtain a marble-like molded product.
以下、本発明を実施例及び比較例により具体的に説明す
る。Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples.
実施例1〜4 温度計、攪拌機を有するフラスコにメタクリル酸メチ
ル1000gとポリエチレングリコール#400ジメタクリレー
ト(NK エステル9G,新中村化学(株)製,商品名)55g
を仕込み、分子量調整剤n−ドデシルメルカプタン5.0g
を加え、80℃まで加温した後、重合開始剤アゾビスイソ
ブチロニトリル0.01gを加え、90℃にて5時間反応を行
ない、粘度4.5poise(MN:42000,MW:450000,MW/MN:10.
7)のA成分(I)を得た。Examples 1 to 4 In a flask having a thermometer and a stirrer, 1000 g of methyl methacrylate and 55 g of polyethylene glycol # 400 dimethacrylate (NK ester 9G, manufactured by Shin-Nakamura Chemical Co., Ltd., trade name)
Was charged, and a molecular weight modifier n-dodecyl mercaptan 5.0 g
After heating to 80 ° C, 0.01 g of azobisisobutyronitrile, a polymerization initiator, was added, and the mixture was reacted at 90 ° C for 5 hours, and had a viscosity of 4.5 poise (MN: 42000, MW: 450,000, MW / MN). :Ten.
7) A component (I) was obtained.
次いで、得られたA成分(I)にB成分を第1表に示
すように加え、それぞれのアクリルシロップ組成物を得
た。なお、B成分であるビニルエステル樹脂の三井東圧
化学(株)社製SM100B−3は、ビスフェノール系エポキ
シ樹脂690gにメタクリル酸200gとトリエチルアミン0.5g
を滴下しながら付加反応して得られたビニルエステル樹
脂に、スチレンモノマー600gを加えてなる2個以上のエ
チレン性不飽和基を有するビニルエステル樹脂60重量%
のアクリルシロップである。また、三井東圧化学(株)
社製SM100B−4は、スチレン、メタクリル酸メチル、グ
リシジルメタアクリレートを共重合させて得られたアク
リルパウダー300gにメタクリル酸メチル100g、スチレン
200gを仕込み、メタクリル酸500gを滴下し、付加反応さ
せてなる、2個以上のエチレン性不飽和基を有するアク
リル樹脂を60重量%含有するアクリルシロップである。Next, B component was added to the obtained A component (I) as shown in Table 1 to obtain respective acrylic syrup compositions. In addition, SM100B-3 manufactured by Mitsui Toatsu Chemicals Co., Ltd., a vinyl ester resin as the B component, is obtained by adding 690 g of a bisphenol-based epoxy resin to 200 g of methacrylic acid and 0.5 g of triethylamine.
Is added to the vinyl ester resin obtained by the addition reaction, and 600 g of a styrene monomer is added to the vinyl ester resin having 60% by weight of a vinyl ester resin having two or more ethylenically unsaturated groups.
Acrylic syrup. In addition, Mitsui Toatsu Chemical Co., Ltd.
Company SM100B-4, styrene, methyl methacrylate, glycidyl methacrylate 300 g of acrylic powder obtained by copolymerization, 100 g of methyl methacrylate, styrene
An acrylic syrup containing 60% by weight of an acrylic resin having two or more ethylenically unsaturated groups, prepared by charging 200 g, dropping 500 g of methacrylic acid, and performing an addition reaction.
実施例5〜8 温度計、攪拌機を有するフラスコにメタクリル酸メチ
ル900gとスチレン100g、トリメチロールプロパントリメ
タクリレート(NK エステルTMPT,新中村化学(株)
製,商品名)20gを仕込み、分子量調整剤n−ドデシル
メルカプタン5.0gを加え、80℃まで加温後、重合開始剤
アゾビスイソブチロニトリル0.01gを加え、90℃にて7
時間反応を行ない、粘度4.3poise(MN:35000,MW:50000
0,MW/MN:14.3)のA成分(II)を得た。Examples 5 to 8 In a flask having a thermometer and a stirrer, 900 g of methyl methacrylate and 100 g of styrene, trimethylolpropane trimethacrylate (NK ester TMPT, Shin-Nakamura Chemical Co., Ltd.)
20 g, and 5.0 g of n-dodecyl mercaptan, a molecular weight modifier, was heated to 80 ° C., and 0.01 g of azobisisobutyronitrile, a polymerization initiator, was added.
Time reaction, viscosity 4.3poise (MN: 35000, MW: 50000)
0, MW / MN: 14.3).
次いで、得られたA成分(II)に実施例1〜4と同様
のB成分を第1表に示すように加え、それぞれのアクリ
ルシロップ組成物を得た。Next, the same B component as in Examples 1 to 4 was added to the obtained A component (II) as shown in Table 1 to obtain respective acrylic syrup compositions.
比較例1〜3 温度計、攪拌機を有するフラスコにメタクリル酸メチ
ル800gとスチレン200g、エチレングリコールジメタクリ
レート(NK エステル1G,新中村化学(株)製,商品
名)5.0gを仕込み、分子量調整剤n−ドデシルメルカプ
タン5.0gを加え、80℃まで加温した後、重合開始剤アゾ
ビスイソブチロニトリル0.01gを加え、90℃にて9時間
反応を行ない、粘度4.5poise(MN:20000,MW:45000,MW/M
N:2.25)のA成分(III)を得た。Comparative Examples 1 to 3 A flask having a thermometer and a stirrer was charged with 800 g of methyl methacrylate, 200 g of styrene, and 5.0 g of ethylene glycol dimethacrylate (NK ester 1G, manufactured by Shin-Nakamura Chemical Co., Ltd., trade name). After adding 5.0 g of dodecyl mercaptan and heating to 80 ° C., 0.01 g of azobisisobutyronitrile polymerization initiator was added, and the mixture was reacted at 90 ° C. for 9 hours, and had a viscosity of 4.5 poise (MN: 20000, MW: 45000, MW / M
N: 2.25) A component (III) was obtained.
次いで、得られたA成分(III)に実施例1〜4と同
様のB成分および市販の低収縮化剤を第1表に示すよう
に加え、それぞれのアクリルシロップ組成物を得た。な
お、ここで用いた市販の低収縮化剤は、ポリ酢酸ビニル
系低収縮化剤である。Next, the same component B as in Examples 1 to 4 and a commercially available low-shrinking agent were added to the obtained component A (III) as shown in Table 1 to obtain respective acrylic syrup compositions. The commercially available low-shrinking agent used here is a polyvinyl acetate-based low-shrinking agent.
得られた成形板の全てについて、以下の評価を行なっ
た。The following evaluations were performed on all of the obtained molded plates.
(成形性) □透明性:光線透過率(%)(日本電色工業(株)製,N
D−101D) □割れ・ひけ:◎……全く生じなかった ○……縁の一部に生じた △……面の一部に生じた ×……全面に生じた (300時間煮沸試験) □白化・黄変:◎……全く生じず、透明であった ○……透明であった △……生じているが、僅かに透明であっ
た ×……不透明であった 〔発明の効果〕 本発明は、特に収縮率を小さくし、成形性を改善し、
さらに、透明性を維持した耐煮沸性に優れたアクリルシ
ロップ組成物である。(Moldability) □ Transparency: Light transmittance (%) (Nippon Denshoku Industries Co., Ltd., N
D-101D) □ Cracks and sink marks:…: Not generated at all…: Generated on a part of the edge △: Generated on a part of the surface ×: Generated on the entire surface (300 hours boiling test) □ Whitening / yellowing:…: Not generated at all, transparent ○: Transparent △: Generated, but slightly transparent ×: opaque [Effect of the Invention] The present invention particularly reduces the shrinkage, improves the moldability,
Furthermore, it is an acrylic syrup composition which is excellent in boiling resistance while maintaining transparency.
Claims (1)
量%からなるアクリルシロップ組成物。 (a)A成分:メタクリル酸メチルを主成分とするエチ
レン性不飽和単量体の総モル数1に対し、架橋性不飽和
単量体を0.002〜0.03モル加え、共重合させて得られる
アクリルシロップのうち、重量平均分子量(MW)が2000
00〜800000、数平均分子量(MN)が20000〜100000で、
その比(MW/MN)が2〜40であるところの高架橋アクリ
ルシロップ。 (b)B成分:エチレン性不飽和単量体を含有し、樹脂
中に少なくとも2つ以上のエチレン性不飽和基を有す
る、ビニルエステル樹脂またはアクリル樹脂を50〜90重
量%含有するアクリルシロップ。1. An acrylic syrup composition comprising the following A component (80 to 20% by weight) and B component (20 to 80% by weight). (A) Component A: Acrylic obtained by adding 0.002 to 0.03 mol of a crosslinkable unsaturated monomer to the total number of moles of ethylenically unsaturated monomer having methyl methacrylate as a main component, and copolymerizing the same. Syrup has a weight average molecular weight (MW) of 2000
00 to 800,000, number average molecular weight (MN) is 2000 to 100,000,
Highly crosslinked acrylic syrup whose ratio (MW / MN) is 2 to 40. (B) Component B: an acrylic syrup containing an ethylenically unsaturated monomer and having 50 to 90% by weight of a vinyl ester resin or an acrylic resin having at least two or more ethylenically unsaturated groups in the resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30760088A JP2707458B2 (en) | 1988-12-05 | 1988-12-05 | Acrylic syrup composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30760088A JP2707458B2 (en) | 1988-12-05 | 1988-12-05 | Acrylic syrup composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02153913A JPH02153913A (en) | 1990-06-13 |
JP2707458B2 true JP2707458B2 (en) | 1998-01-28 |
Family
ID=17971004
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30760088A Expired - Fee Related JP2707458B2 (en) | 1988-12-05 | 1988-12-05 | Acrylic syrup composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2707458B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003073430A (en) * | 2001-09-04 | 2003-03-12 | Sumitomo Chem Co Ltd | Resin composition, molded article and method for producing molded article |
EP2740764A4 (en) * | 2012-02-13 | 2014-09-17 | Panasonic Corp | RESIN COMPOSITION (METH) ACRYLATE AND CURED PRODUCT USING THE SAME |
JP6189613B2 (en) * | 2013-03-18 | 2017-08-30 | スタンレー電気株式会社 | Aspherical lens and manufacturing method thereof |
JPWO2015025876A1 (en) * | 2013-08-20 | 2017-03-02 | 三菱レイヨン株式会社 | Dispersed acrylic copolymer |
-
1988
- 1988-12-05 JP JP30760088A patent/JP2707458B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH02153913A (en) | 1990-06-13 |
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