JP2017505706A - 基体上の老朽化被覆層を覆うための方法及び該方法における使用に好適な被覆組成物 - Google Patents
基体上の老朽化被覆層を覆うための方法及び該方法における使用に好適な被覆組成物 Download PDFInfo
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- JP2017505706A JP2017505706A JP2016535052A JP2016535052A JP2017505706A JP 2017505706 A JP2017505706 A JP 2017505706A JP 2016535052 A JP2016535052 A JP 2016535052A JP 2016535052 A JP2016535052 A JP 2016535052A JP 2017505706 A JP2017505706 A JP 2017505706A
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- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- XNFIRYXKTXAHAC-UHFFFAOYSA-N tralopyril Chemical compound BrC1=C(C(F)(F)F)NC(C=2C=CC(Cl)=CC=2)=C1C#N XNFIRYXKTXAHAC-UHFFFAOYSA-N 0.000 description 1
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- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- XVZMLSWFBPLMEA-UHFFFAOYSA-N trimethoxy(2-pyridin-2-ylethyl)silane Chemical compound CO[Si](OC)(OC)CCC1=CC=CC=N1 XVZMLSWFBPLMEA-UHFFFAOYSA-N 0.000 description 1
- FTDRQHXSYGDMNJ-UHFFFAOYSA-N trimethoxy(3-pyrrol-1-ylpropyl)silane Chemical compound CO[Si](OC)(OC)CCCN1C=CC=C1 FTDRQHXSYGDMNJ-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
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- 238000005303 weighing Methods 0.000 description 1
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- 229910052725 zinc Inorganic materials 0.000 description 1
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- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
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Abstract
Description
a)硬化性又は架橋性のオルガノシロキサンポリマー、有機ビスマス化合物及びシランカップリング剤を含む被覆組成物を提供すること、
b)前記被覆組成物の層を老朽化被覆層に塗布すること、及び
c)前記被覆組成物を硬化及び/又は架橋させて、硬化及び/又は架橋させられた被覆層を形成すること
によって覆う方法であって、
老朽化被覆層が、6ヶ月よりも前に塗布された被覆層である、方法に関連する。
a)線状及びトリフルオロメチル分岐のフッ素エンドキャップ処理ペルフルオロポリエーテル(例えば、Fomblin Y(登録商標)、Krytox K(登録商標)液、又は、Demnum S(登録商標)オイル);
b)線状のジオルガノ(OH)エンドキャップ処理ペルフルオロポリエーテル(例えば、Fomblin Z DOL(登録商標)、Fluorolink E(登録商標));
c)低MWのポリクロロトリフルオロエチレン(例えば、Daifloil CTFE(登録商標)液など)。
Q3Si−O−(SiQ2−O−)nSiQ3
式中、それぞれの基において、Qは、1個〜10個の炭素原子を有する炭化水素鎖を表し、nは、シリコーンオイルが20mPa s〜5000mPa sの粘性を有するような整数である。Q基の少なくとも10%が一般にはメチル基であり、Q基の少なくとも2%がフェニル基である。最も好ましくは、−SiQ2−O−ユニットの少なくとも10%がメチル−フェニルシロキサンユニットである。最も好ましくは、上記シリコーンオイルはメチル終端ポリ(メチルフェニルシロキサン)である。このオイルは好ましくは、粘性が20mPa s〜1000mPa sである。好適なシリコーンオイルの様々な例が、Bluestar Siliconesによって、Rhodorsil Huile 510V100、及び、Rhodorsil Huile 550の商標で販売されている。シリコーンオイルにより、水生動植物汚損に対する被覆物系の耐性が改善される。
P1-Si(P2)2-[-O-Si(P3)2-]a-[-O-Si(P3)(P4)-]b-O-Si(P2)2-P1
式中、
・P1は、同じ又は異なっていてもよく、アルキル基、アリール基及びアルケニル基から選択され、但し、アルキル基、アリール基及びアルケニル基は必要に応じて、アミン基、式OP5の酸素含有基(式中、P5は水素又はC1〜6アルキルである)、及び、−P6−N(P7)−C(O)−P8−C(O)−XP3に従う官能基
(式中、
・P6は、1個〜12個の炭素原子のアルキル、ヒドロキシアルキル、カルボキシアルキル、及び、10個までの炭素原子のポリオキシアルキレンから選択される;
・P7は、水素、1個〜6個の炭素原子のアルキル、ヒドロキシアルキル、カルボキシアルキル、及び、1個〜10個の炭素原子のポリオキシアルキレンから選択される;P7は、環を形成するためにP8に結合する場合がある;
・P8は、1個〜20個の炭素原子を有するアルキル基である;
・P9は、水素、又は、1個〜10個の炭素原子を有するアルキル基(但し、アルキル基は必要に応じて、酸素含有基又は窒素含有基により置換される)である;
・Xは、O、S及びNHから選択される)
から選択される;
・但し、オルガノシリコーンポリマーにおける少なくとも1つのP1基が、上記式に従う官能基又はその塩誘導体である;
・P2は、同じ又は異なっていてもよく、アルキル、アリール及びアクレニル(aklenyl)から選択される;
・P3及びP4(これらは同じ又は異なっていてもよい)は、アルキル、アリール、キャップ化又は非キャップ化のポリオキシアルキレン、アルカリール、アラルキレン及びアルケニルから選択される;
・aは0〜50,000の整数である;
・bは0〜100の整数である;かつ
・a+bは少なくとも25である。
・P2、P3及びP4は独立して、メチル及びフェニルから選択され、より好ましくはメチルである。
・P6は、1個〜12個の炭素原子を有するアルキル基であり、より好ましくは2個〜5個の炭素原子を有するアルキル基である。
・P7は、水素、又は、1個〜4個の炭素原子を有するアルキル基である。
・P8は、2個〜10個の炭素原子を有するアルキル基である。
・P9は、水素、又は、1個〜5個の炭素原子を有するアルキル基である。
・Xは酸素原子である。
・a+bは100から300にまで及ぶ。
a)硬化性又は架橋性のオルガノシロキサンポリマー、有機ビスマス化合物及びシランカップリング剤(これらは、本明細書中においてさらに詳しく記載される通りである)を含む被覆組成物を提供すること、
b)前記被覆組成物の少なくとも1つの層を基体上の老朽化被覆層に塗布すること、
c)前記少なくとも1つの層の被覆組成物を硬化及び/又は架橋させて、硬化及び/又は架橋させられた被覆層を前記基体に形成すること、及び
d)前記被覆された基体を水域環境に置くこと
によって防止する方法であって、
老朽化被覆層が、6ヶ月よりも前に塗布された被覆層である、方法に関連する。
被覆組成物の実施例A〜実施例Fを、各成分を適切な金属容器に(小数点以下2桁の天秤で)正確に計り取り、気密蓋で密封することによって調製した。これらの被覆物はその後、ブラシにより基体に塗布する1分前に、パレットナイフを使用して混合された。成分が表1に列挙される。実施例Bが、本発明に従うものである。それ以外の実施例は比較用の実施例である。
接着試験が、被覆物を基体に塗布し、乾燥させた48時間後に行われる。試験を、X印をナイフで被覆物に切り込むことによって行う。X印をその後、2つの被覆物の間の接着における何らかの弱いところを強調するために布きれでこすった。塗膜間の接着に、表3に示される評価システムを使用して、0〜5のスコアを与えた。
Claims (15)
- a)硬化性又は架橋性のオルガノシロキサンポリマー、有機ビスマス化合物及びシランカップリング剤を含む被覆組成物を提供すること、
b)前記被覆組成物の層を基体上の老朽化被覆層に塗布すること、
c)前記被覆組成物を硬化及び/又は架橋させて、硬化及び/又は架橋させられた被覆層を形成すること
によって基体上の老朽化被覆層を覆う方法であって、
老朽化被覆層が6ヶ月よりも前に塗布された被覆層である、方法。 - 前記老朽化被覆層は硬化又は架橋させられたオルガノシロキサンポリマーを含む、請求項1に記載の方法。
- 工程c)で形成される前記硬化させられた被覆層は水域環境における汚損を阻止することができる汚損剥離被覆物である、請求項1又は2のいずれかに記載の方法。
- 前記老朽化被覆層は、水没及び非水没を交互に受けることになる人工構造物のある領域、例えば船の外殻に位置する老朽化した汚損剥離被覆層である、請求項1から3のいずれかに記載の方法。
- 工程c)で形成される前記硬化させられた被覆層がさらに1つ又はそれ以上の被覆組成物の層により覆われる、請求項1から4のいずれかに記載の方法。
- 前記シランカップリング剤がアミノ官能性シラン又はエポキシ官能性シランである、請求項1から5のいずれかに記載の方法。
- 前記シランカップリング剤がC2〜C10アルコキシ基を含むアミノ官能性シランである、請求項6に記載の方法。
- 前記シランカップリング剤がアミノシラン、例えばN−2−アミノエチル−3−アミノプロピルトリメトキシシランなどである、請求項1から7のいずれかに記載の方法。
- 前記有機ビスマス化合物がビスマスのカルボン酸塩、例えばネオデカン酸ビスマスである、請求項1から8のいずれかに記載の方法。
- 前記被覆組成物が、0.2重量%〜2.0重量%の前記有機ビスマス化合物と、0.1重量%〜1.0重量%の前記シランカップリング剤とを含む(但し、重量は被覆組成物の総重量に基づく)、請求項1から9のいずれかに記載の方法。
- 前記硬化性オルガノシロキサンポリマーは、一般構造−[SiR1R2−O]−の繰り返しユニット(式中、R1及びR2は独立して、水素、アルキル、アリール、アラルキル、及びビニル基から選択される)を含む、請求項1から10のいずれかに記載の方法。
- R1及びR2が独立してメチル及びフェニルから選択され、好ましくはR1及びR2がメチルである、請求項11に記載の方法。
- 請求項1から12のいずれかに記載される方法に従って被覆されている、水没及び非水没を交互に受けることになる基体、例えば船殻。
- a)硬化性又は架橋性のオルガノシロキサンポリマー、有機ビスマス化合物及びシランカップリング剤を含む被覆組成物を提供すること、
b)前記被覆組成物の少なくとも1つの層を基体上の老朽化被覆層に塗布すること、
c)前記少なくとも1つの被覆組成物の層を硬化及び/又は架橋させて、硬化及び/又は架橋させられた被覆層を前記基体に形成すること、及び
d)前記被覆された基体を水域環境に置くこと
によって水域環境における基体の汚損を防止する方法であって、
老朽化被覆層が6ヶ月よりも前に塗布された被覆層である、方法。 - 水域環境におけるバイオフィルム及び/又は水生生物の汚損を防止するための老朽化被覆層により既に覆われている基体における、請求項1から12のいずれかで定義されるような被覆組成物の被覆物としての使用であって、老朽化被覆層が6ヶ月よりも前に塗布された被覆層である、使用。
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- 2014-12-01 US US15/039,274 patent/US20170051159A1/en not_active Abandoned
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JP2021080336A (ja) * | 2019-11-15 | 2021-05-27 | 谷口 孝 | 撥水性に優れた硬化性樹脂組成物 |
JP7357870B2 (ja) | 2019-11-15 | 2023-10-10 | 孝 谷口 | 撥水性に優れた硬化性樹脂組成物 |
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ES2666412T3 (es) | 2018-05-04 |
JP6385437B2 (ja) | 2018-09-05 |
AU2014359446A1 (en) | 2016-05-26 |
EP3077468B1 (en) | 2018-02-28 |
MX2016006848A (es) | 2016-09-13 |
CN105745290B (zh) | 2021-03-23 |
EP3077468A2 (en) | 2016-10-12 |
WO2015082408A2 (en) | 2015-06-11 |
KR20160091915A (ko) | 2016-08-03 |
CN105745290A (zh) | 2016-07-06 |
US20170051159A1 (en) | 2017-02-23 |
DK3077468T3 (en) | 2018-05-22 |
CL2016001296A1 (es) | 2016-10-28 |
KR102354241B1 (ko) | 2022-01-21 |
WO2015082408A3 (en) | 2016-04-14 |
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