JPH0451573B2 - - Google Patents
Info
- Publication number
- JPH0451573B2 JPH0451573B2 JP28529386A JP28529386A JPH0451573B2 JP H0451573 B2 JPH0451573 B2 JP H0451573B2 JP 28529386 A JP28529386 A JP 28529386A JP 28529386 A JP28529386 A JP 28529386A JP H0451573 B2 JPH0451573 B2 JP H0451573B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- component
- acrylate
- methacrylate
- 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
Links
- 239000000178 monomer Substances 0.000 claims description 20
- 239000008199 coating composition Substances 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000000694 effects Effects 0.000 description 9
- 230000002265 prevention Effects 0.000 description 9
- 239000000203 mixture Substances 0.000 description 6
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- XHAFIUUYXQFJEW-UHFFFAOYSA-N 1-chloroethenylbenzene Chemical compound ClC(=C)C1=CC=CC=C1 XHAFIUUYXQFJEW-UHFFFAOYSA-N 0.000 description 1
- OLQFXOWPTQTLDP-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCO OLQFXOWPTQTLDP-UHFFFAOYSA-N 0.000 description 1
- RWXMAAYKJDQVTF-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl prop-2-enoate Chemical compound OCCOCCOC(=O)C=C RWXMAAYKJDQVTF-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-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
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-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
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- YKXAYLPDMSGWEV-UHFFFAOYSA-N 4-hydroxybutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCO YKXAYLPDMSGWEV-UHFFFAOYSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 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
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 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
- 238000001035 drying Methods 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
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- MDNFYIAABKQDML-UHFFFAOYSA-N heptyl 2-methylprop-2-enoate Chemical compound CCCCCCCOC(=O)C(C)=C MDNFYIAABKQDML-UHFFFAOYSA-N 0.000 description 1
- SCFQUKBBGYTJNC-UHFFFAOYSA-N heptyl prop-2-enoate Chemical compound CCCCCCCOC(=O)C=C SCFQUKBBGYTJNC-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 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
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 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
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- -1 α-alkylstyrene Chemical compound 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Description
(発明の利用分野)
本発明は、被覆用組成物、特に可塑化ポリ塩化
ビニル用の被覆用組成物に関する。
(従来技術)
近年、各種基材表面に汚れ防止機能を付与する
要望が高く、多くの被覆用組成物が提案されてい
る。例えば、メチルメタクリレートを主体とした
重合体を被覆する方法あるいは、さらにフツ素系
モノマーやシリコン系モノマーとの共重合体を被
覆組成物として使用することが提案されている。
従来、この種の被覆用組成物の適用例として
は、繊維やじゆうたんに揆水揆油機能を付与する
ことが知られている。
この場合、シリコン樹脂の本来の機能は発揮し
ているが可塑化ポリ塩化ビニルを基材とする表面
に使用した場合は上記性質に同時に要求される汚
れ防止効果が得られなかつた。
この理由は明らかではないが基材が異なると、
同質の作用を示すとは考えられない面があり、こ
のような欠点を解決できる被覆用組成物の開発が
望まれていた。
(発明が解決しようとする問題点)
本発明の目的は、基材との密着に優れ、かつ長
期間優れた汚れ防止機能を発揮する被覆用組成物
を提供することである。
(問題を解決するための手段)
本発明を概説すると、
A 構造式
で表わされる単量体1〜40重量%
B (イ) アクリル酸又はメタクリル酸アルキルエ
ステル 40〜95重量部
(ロ) α、β−エチレン性不飽和カルボン酸のヒ
ドロキシアルキル含有エステル 5〜20重量部
(ハ) その他の共重合性ビニル単量体
0〜40重量部
よりなる単量体99〜60重量%を構成単量体とする
重合体を塗膜形成成分とする被覆用組成物に関す
る。
本発明者等の研究によると前記従来知られてい
る汚れ防止剤のフツ素系共重合体やシリコン系共
重合体を被覆して形成される塗膜は架橋による高
分子化がなされておらず、このために汚れ防止機
能が持続しないという知見を得た。
本発明は、この知見に基づき完成したもので、
シリコン含有単量体とα、β−エチレン性不飽和
単量体組成とを構成単量体とする重合体を製造す
る場合に、分子内にOH基を含有する架橋性単量
体を必須単量体成分として重合させることによ
り、汚れ防止機能を長時間持続させることに成功
したのである。
本発明をより詳細に説明すると、被覆用組成物
の塗膜形成成分のうち、A、成分のシリコン含有
単量体としては、次に示す構造式で表わされる化
合物を使用する。
この場合、分子中のメチレン基の数(m)を1
〜6に限定するのは、6以上になれば共重合性に
劣るためである。
B成分の単量体組成としては、(イ)アクリル酸又
はメタクリル酸アルキルエステル、(ロ)α、β−エ
チレン性不飽和カルボン酸のヒドロキシアルキル
含有エステルおよび(ハ)その他の共重合性ビニル単
量体よりなるものである。
アクリル酸又はメタクリル酸アルキルエステル
の例としては、メチルアクリレート、メチルメタ
ルクリレート、エチルアクリレート、エチルメタ
クリレート、n−プロピルアクリレート、n−プ
ロピルメタクリレート、イソプロピルアクリレー
ト、イソプロピルメタクリレート、ブチルアクリ
レート、ブチルメタクリレート、ラウリルアクリ
レート、ラウリルメタクリレート、ステアリルア
クリレート、ステアリルメタクリレート、ヘキシ
ルアクリレート、2−エチルヘキシルメタクリレ
ート、ヘプチルアクリレート、ヘプチルメタクリ
レートなどがあり、アルキル基内に炭素原子約20
までを有する同様なエステルが使用できる。
(ロ)成分のα、β−エチレン性不飽和カルボン酸
のヒドロキシアルキル含有エステルとしては、2
−ヒドロキシエチルアクリレート、2−ヒドロキ
シエチルメタクリレート、2−ヒドロキシプロピ
ルアクリレート、2−ヒドロキシプロピルメタク
リレート、3−ヒドロキシプロピルアクリレー
ト、3−ヒドロキシプロピルメタクリレート、4
−ヒドロキシブチルメタクリレート、ジエチレン
グリコールモノアクリレート、ジエチレングリコ
ールモノメタクリレートなどが使用できる。
(ハ)成分のその他の共重合性ビニル単量体として
は、スチレン、α−アルキルスチレン、α−クロ
ロスチレン、ビニルトルエン、アクリロニトリ
ル、酢酸ビニル等がある。
B成分の単量体組成物の使用割合は、(イ)成分が
40〜95重量部、(ロ)成分が5〜20重量部、及び(ハ)成
分が0〜40重量部の範囲である。
本発明においては、特に(ロ)成分の配合量が汚れ
防止効果の長期持続性に影響を及ぼし、(ロ)成分が
5重量部未満であれば、持続性が得られず、一方
20重量部を越えると、塗膜に粘着性が生じる原因
となり好ましくない。
本発明では、A成分とB成分の組成配合は、A
成分1〜40重量%、B成分60〜99重量%の割合と
することが必要である。
これは、A成分が1重量%未満では、汚れ防止
効果の長期持続性に影響を及ぼし、一方40重量%
を越えるとシリコン基の揆水、揆油性による汚れ
防止効果より、粘着性が増し汚れ防止効果が悪く
なるためである。
本発明における重合反応は、A成分とB成分を
混合撹拌の後、フラスコ中に数回に分けて分添
し、還流温度で8〜12時間撹拌を行つてなされ
る。本発明で使用する有機溶剤としては、メタノ
ール、エタノール、プロパノール等のアルコール
系、アセトン、メチルエチルケトン、メチルイソ
ブチルケトン、シクロヘキサノン等のケトン系、
酢酸エチル、酢酸ブチル等のエステル系、及びベ
ンゼン、トルエン、キシレン等の炭化水素系が適
当である。本発明の被覆用組成物は、可塑化ポリ
塩化ビニルを基材とするテント、シート、成形
品、人造レザー、壁紙等の表面被覆に適してい
る。
しかし、可塑化ポリ塩化ビニルを基材とする場
合、可塑剤のブリードにより被覆膜の密着が悪く
なることがあり、可塑剤のブリードを防止する目
的で、プライマー層を形成することが好ましい。
以下、本発明をより具体的に説明するため実施
例を示す。なお実施例中、部はすべて重量部であ
る。
実施例 1
かくはん装置、温度計及び還流冷却器を備えた
3四つ口フラスコに、シリコン系アクリルモノ
マー(商品名X−22−5002 信越化学社製)5
部、メチルメタクリレート75部、2−エチルヘキ
シルアクリレート5部、2−ヒドロキシエチルア
クリレート5部、スチレン10部、ジターシヤリー
ブチルパーオキサイド3部、トルエン100部を仕
込み還流下で、8時間撹拌を行い共重合体を調製
した。ついで、トルエン312部を加えて樹脂固形
分を20重量%に調製した被覆用組成物をえた。
実施例2〜4及び比較例1〜4
実施例1と同様の方法において、単量体組成を
第1表に示す内容にかえる以外はすべて同じ方法
で反応を行い共重合体を調製し、さらにトルエン
を加えて樹脂固形分が20重量%の被覆用組成物を
それぞれえた。
FIELD OF THE INVENTION The present invention relates to coating compositions, in particular coating compositions for plasticized polyvinyl chloride. (Prior Art) In recent years, there has been a strong demand for imparting stain prevention functions to the surfaces of various substrates, and many coating compositions have been proposed. For example, it has been proposed to coat with a polymer mainly composed of methyl methacrylate, or to use a copolymer with a fluorine-based monomer or a silicon-based monomer as a coating composition. Conventionally, as an example of application of this type of coating composition, it has been known to impart a water-repelling oil function to fiber yarn. In this case, although the original function of the silicone resin was exhibited, when it was used on a surface based on plasticized polyvinyl chloride, the stain prevention effect required at the same time as the above-mentioned properties could not be obtained. The reason for this is not clear, but when the base material is different,
In some respects, it is difficult to believe that they would exhibit the same effects, and it has been desired to develop a coating composition that can solve these drawbacks. (Problems to be Solved by the Invention) An object of the present invention is to provide a coating composition that has excellent adhesion to a substrate and exhibits an excellent stain prevention function for a long period of time. (Means for solving the problem) To outline the present invention, A Structural formula 1 to 40% by weight of the monomer represented by B (a) Acrylic acid or methacrylic acid alkyl ester 40 to 95 parts by weight (b) Hydroxyalkyl-containing ester of α,β-ethylenically unsaturated carboxylic acid 5 to 20 parts by weight (c) Other copolymerizable vinyl monomers
The present invention relates to a coating composition whose film-forming component is a polymer containing 99 to 60% by weight of monomers consisting of 0 to 40 parts by weight. According to the research conducted by the present inventors, the coating film formed by coating the fluorine-based copolymer or silicone-based copolymer of the conventionally known antifouling agent is not polymerized by crosslinking. It was found that the stain prevention function does not last for this reason. The present invention was completed based on this knowledge,
When producing a polymer having a silicon-containing monomer and an α,β-ethylenically unsaturated monomer composition as constituent monomers, a crosslinkable monomer containing an OH group in the molecule is used as an essential monomer. By polymerizing it as a polymeric component, they were able to maintain its stain prevention function for a long time. To explain the present invention in more detail, among the coating film forming components of the coating composition, as component A, a silicon-containing monomer, a compound represented by the following structural formula is used. In this case, the number of methylene groups in the molecule (m) is 1
The reason why it is limited to 6 to 6 is because if it is 6 or more, copolymerizability is poor. The monomer composition of component B includes (a) acrylic acid or methacrylic acid alkyl ester, (b) hydroxyalkyl-containing ester of α,β-ethylenically unsaturated carboxylic acid, and (c) other copolymerizable vinyl monomers. It consists of a quantity. Examples of acrylic acid or methacrylic acid alkyl esters include methyl acrylate, methyl metal acrylate, ethyl acrylate, ethyl methacrylate, n-propyl acrylate, n-propyl methacrylate, isopropyl acrylate, isopropyl methacrylate, butyl acrylate, butyl methacrylate, lauryl acrylate. , lauryl methacrylate, stearyl acrylate, stearyl methacrylate, hexyl acrylate, 2-ethylhexyl methacrylate, heptyl acrylate, heptyl methacrylate, etc., which have about 20 carbon atoms in the alkyl group.
Similar esters with up to can be used. (B) As the hydroxyalkyl-containing ester of α,β-ethylenically unsaturated carboxylic acid, 2
-Hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, 3-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 4
-Hydroxybutyl methacrylate, diethylene glycol monoacrylate, diethylene glycol monomethacrylate, etc. can be used. Other copolymerizable vinyl monomers of component (iii) include styrene, α-alkylstyrene, α-chlorostyrene, vinyltoluene, acrylonitrile, vinyl acetate, and the like. The usage ratio of the monomer composition of component B is as follows:
The range is 40 to 95 parts by weight, 5 to 20 parts by weight of component (b), and 0 to 40 parts by weight of component (c). In the present invention, the blending amount of component (B) in particular affects the long-term sustainability of the stain prevention effect, and if component (B) is less than 5 parts by weight, sustainability cannot be obtained;
If it exceeds 20 parts by weight, it is undesirable because it causes the coating film to become sticky. In the present invention, the composition of component A and component B is
It is necessary to set the proportions to be 1 to 40% by weight of component and 60 to 99% by weight of component B. This means that if the A component is less than 1% by weight, it will affect the long-term sustainability of the stain prevention effect, whereas if the A component is less than 1% by weight, the
This is because, if it exceeds the stain-preventing effect due to the water-repellent and oil-repellent properties of the silicone base, the tackiness increases and the stain-preventing effect becomes worse. The polymerization reaction in the present invention is carried out by mixing and stirring component A and component B, then adding the mixture in several portions into a flask, and stirring at reflux temperature for 8 to 12 hours. Examples of organic solvents used in the present invention include alcohols such as methanol, ethanol, and propanol; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone;
Ester systems such as ethyl acetate and butyl acetate, and hydrocarbon systems such as benzene, toluene and xylene are suitable. The coating composition of the present invention is suitable for surface coating of tents, sheets, molded articles, artificial leather, wallpaper, etc., which are based on plasticized polyvinyl chloride. However, when plasticized polyvinyl chloride is used as a base material, the adhesion of the coating film may deteriorate due to bleeding of the plasticizer, so it is preferable to form a primer layer for the purpose of preventing bleeding of the plasticizer. Examples will be shown below to more specifically explain the present invention. In the examples, all parts are parts by weight. Example 1 Silicone-based acrylic monomer (trade name:
75 parts of methyl methacrylate, 5 parts of 2-ethylhexyl acrylate, 5 parts of 2-hydroxyethyl acrylate, 10 parts of styrene, 3 parts of ditertiary butyl peroxide, and 100 parts of toluene were charged and stirred for 8 hours under reflux. A polymer was prepared. Then, 312 parts of toluene was added to obtain a coating composition having a resin solid content of 20% by weight. Examples 2 to 4 and Comparative Examples 1 to 4 Copolymers were prepared by carrying out reactions in the same manner as in Example 1, except that the monomer composition was changed to that shown in Table 1. Toluene was added to obtain each coating composition with a resin solids content of 20% by weight.
【表】
|
CH3
実験例
実施例1〜4及び比較例1〜4でえられた被覆
用組成物を用いて、PVC帆布(商品名 クラフ
タ−K355 クラレ社製)にグラビアプリンター
(95メツシユ)で塗布し、80℃で1分乾燥させて
塗布片を作成した。
それぞれの塗布片の性能をテストした結果は第
2表に示す通りであつた。【table】
|
CH3
Experimental Example Using the coating compositions obtained in Examples 1 to 4 and Comparative Examples 1 to 4, the coating compositions obtained in Examples 1 to 4 and Comparative Examples 1 to 4 were applied to a PVC canvas (trade name: Crafter K355, manufactured by Kuraray Co., Ltd.) using a gravure printer (95 mesh), and heated at 80°C. After drying for 1 minute, a coated piece was prepared. The performance of each coated piece was tested and the results are shown in Table 2.
【表】
ただし、汚れ防止性試験は、次のようにして行
つた。
塗布片(3cm×3cm)を第3表に示す汚れ成分
を入れたガラス容器に浸し80℃の乾燥機中で15分
間放置した後、さらにこれを3分間振盪するとい
う操作を4回くり返し、塗布片をとり出して水で
洗浄の後、その表面の汚れの割合を目視で判定し
た。
又、耐屈曲性試験は、塗布片を屈曲試験機に取
付け、1万回の屈曲を行なつた後、前記の汚れ成
分中に塗布片を入れ、3分間振盪した後とり出し
て、表面のクラツク発生割合を目視で判定した。
さらに、耐候性試験は、サンシヤインウエザー
オメータにて試験した後、塗布片表面のクラツク
発生割合を目視で判定した。
表中、
◎…全くなく優れる
○…少し発生
△…目立つ程度に発生
×…全面発生[Table] However, the stain prevention test was conducted as follows. A coated piece (3 cm x 3 cm) was immersed in a glass container containing the stain components shown in Table 3, left in a dryer at 80°C for 15 minutes, and then shaken for an additional 3 minutes. Repeat this process 4 times. After removing the piece and washing it with water, the percentage of dirt on its surface was visually determined. In addition, in the bending resistance test, the coated piece was attached to a bending tester and flexed 10,000 times, then the coated piece was placed in the dirt component mentioned above, shaken for 3 minutes, taken out, and the surface The crack occurrence rate was determined visually. Furthermore, the weather resistance test was conducted using a sunshine weather meter, and then the crack occurrence rate on the surface of the coated piece was visually determined. In the table, ◎...Not at all, excellent ○...Slight occurrence △...Conspicuous occurrence ×...Full surface occurrence
【表】【table】
【表】
(発明の効果)
以上の説明により明らかなように、本発明の被
覆用組成物は、汚れ防止性に優れ、しかもその効
果が長期間にわたり継続され、しかも屈曲しても
クラツクが入りにくいという作用効果を奏するも
のである。[Table] (Effects of the Invention) As is clear from the above explanation, the coating composition of the present invention has excellent stain prevention properties, maintains this effect for a long period of time, and does not crack even when bent. It has the effect of being difficult to use.
Claims (1)
ステル 40〜95重量部 (ロ) α、β−エチレン性不飽和カルボン酸のヒ
ドロキシアルキル含有エステル 5〜20重量部 (ハ) その他の共重合性ビニル単量体
0〜40重量部 よりなる単量体99〜60重量%を構成単量体とする
重合体を塗膜形成成分とする被覆用組成物。[Claims] 1 A Structural formula 1 to 40% by weight of the monomer represented by B (a) Acrylic acid or methacrylic acid alkyl ester 40 to 95 parts by weight (b) Hydroxyalkyl-containing ester of α,β-ethylenically unsaturated carboxylic acid 5 to 20 parts by weight (c) Other copolymerizable vinyl monomers
A coating composition whose coating film-forming component is a polymer containing 99 to 60% by weight of monomers consisting of 0 to 40 parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28529386A JPS63137934A (en) | 1986-11-28 | 1986-11-28 | Coating composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28529386A JPS63137934A (en) | 1986-11-28 | 1986-11-28 | Coating composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63137934A JPS63137934A (en) | 1988-06-09 |
| JPH0451573B2 true JPH0451573B2 (en) | 1992-08-19 |
Family
ID=17689647
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28529386A Granted JPS63137934A (en) | 1986-11-28 | 1986-11-28 | Coating composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63137934A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01131254A (en) * | 1987-08-14 | 1989-05-24 | Mitsubishi Kasei Vinyl Co | Molded vinyl chloride based resin product |
-
1986
- 1986-11-28 JP JP28529386A patent/JPS63137934A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63137934A (en) | 1988-06-09 |
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