JP2000001637A5 - - Google Patents
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- JP2000001637A5 JP2000001637A5 JP1998166470A JP16647098A JP2000001637A5 JP 2000001637 A5 JP2000001637 A5 JP 2000001637A5 JP 1998166470 A JP1998166470 A JP 1998166470A JP 16647098 A JP16647098 A JP 16647098A JP 2000001637 A5 JP2000001637 A5 JP 2000001637A5
- Authority
- JP
- Japan
- Prior art keywords
- release agent
- independently
- solvent
- water
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 239000003795 chemical substances by application Substances 0.000 claims description 16
- -1 Ethylene, propylene, butylene Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims description 4
- 239000003586 protic polar solvent Substances 0.000 claims description 3
- 239000003973 paint Substances 0.000 description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N methylene dichloride Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N n-methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- DRLRGHZJOQGQEC-UHFFFAOYSA-N 2-(2-methoxypropoxy)propyl acetate Chemical compound COC(C)COC(C)COC(C)=O DRLRGHZJOQGQEC-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atoms Chemical group C* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 230000001590 oxidative Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N γ-lactone 4-hydroxy-butyric acid Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 1
Description
【0002】
【従来の技術】
従来建造物等外壁の再塗装の為に旧塗膜を剥離する場合や、建造物床材等に用いるプラ
スティックタイルの敷き直しをする場合、剥離時間の短縮並びに作業の省力化を目的とし
て剥離剤が用いられてきた。この剥離剤は塩化メチレンを主成分とした塗料剥離剤や強ア
ルカリ水溶性の塗料剥離剤が主である。しかし昨今、環境意識の高まり等から、塩化メチ
レンを主剤とした塗料剥離剤やアルカリ水溶性塗料剥離剤を使用せず、物理的に剥離する
手法が試みられるようになった。0002.
[Conventional technology]
When peeling off the old paint film for repainting the outer wall of a conventional building, or when re-laying plastic tiles used for building flooring, etc., a peeling agent for the purpose of shortening the peeling time and saving labor. Has been used. This release agent is mainly a paint release agent containing methylene chloride as a main component and a strong alkali water-soluble paint release agent. However, in recent years, due to heightened environmental awareness, a method of physically peeling without using a paint stripper containing methylene chloride as a main component or an alkaline water-soluble paint stripper has been tried.
塩化メチレンを主剤とする剥離剤は環境影響や作業安全性、毒性の懸念があり、又、他の塩素系有機溶剤も環境問題を引き起こす可能性がある。強アルカリ水溶性剥離剤は、水酸化アルカリ金属による樹脂の酸化劣化をベースとする。上記同様に添加される促進剤の安定性、作業の安全性及び廃棄物処理が問題となっている。またかかる問題を解決するため、非塩素系溶剤型剥離剤が多数開発されているが、引火性の問題があったり、引火点を消したり水溶性化合物を添加するために有機溶剤が本来持つ剥離除去性能を犠牲にして水等を添加しいるものが殆どで、多くの非塩素系有機溶剤型剥離剤が含むN−メチル−2−ピロリドンは、不快なアミン臭を持ち、塩基性化合物の存在下では安定でない。A release agent containing methylene chloride as a main component has concerns about environmental impact, work safety, and toxicity, and other chlorine- based organic solvents may also cause environmental problems. The strong alkali water-soluble release agent is based on the oxidative deterioration of the resin due to the alkali metal hydroxide. The stability of the accelerator added in the same manner as described above, the safety of work, and the waste treatment are problems. In addition, many non-chlorine solvent type release agents have been developed to solve this problem, but there is a problem of flammability, and the release inherent in organic solvents to extinguish the flash point or add a water-soluble compound. Most of them add water etc. at the expense of removal performance, and N-methyl-2-pyrrolidone contained in many non-chlorine organic solvent type release agents has an unpleasant amine odor and the presence of basic compounds. Not stable below.
また、これらの非塩素系溶剤型剥離剤を外壁塗膜等に用いた場合、塗膜表面を急激に溶解する為、剥離剤が滑り落ちてしまう。また、溶解した塗膜は乾燥前の塗料と同一の状態となり、剥離剤の塗布効率及び作業場所への再付着、塗料の廃棄物処理等、全体的な作業効率が著しく低下する。この為、一般的には工場内作業等にて剥離剤に浸漬するような用途に使用されているのみである。In the case of using these non-chlorine-based solvent type release agent to the outer wall coating or the like, in order to rapidly dissolve the coating surface, the release agent will slide down. In addition, the dissolved coating film is in the same state as the paint before drying, and the overall work efficiency such as the application efficiency of the release agent, reattachment to the work place, and waste treatment of the paint is significantly reduced. For this reason, it is generally only used for applications such as immersing in a release agent in factory work or the like.
【0007】
【課題を解決するための手段】
上記問題点を解決するための本発明の剥離剤は、第1に下記(ア),(イ),(ウ)を
含み、且つ実質量の塩素化溶剤を含まない組成物からなることを特徴としている。
(ア)95〜10w%の下式Iのエチレン、プロピレン、ブチレングリコールエーテルエ
ステル
O
‖
R1O−(CH2−CHR2O)n−C−R3 (I)
(上式中、R 1 は独立にC 1 〜C 4 アルキル基でR 2 は独立に水素、メチル、エチルであり、
R 3 は独立にC 1 〜C 4 アルキル基であり、nは1〜4である)
(イ)0〜30w%の有機プロトン性溶媒
(ウ)5〜80w%の水
第2に有機プロトン性溶媒が3〜18個の炭素原子を有するアルコールであることを特
徴としている。
第3に塩基性もしくは酸性化合物を含むことを特徴としている。
第4に上記記載の組成物を増粘し、塗布性及び作業性を改善したことを特徴としている
。0007
[Means for solving problems]
The release agent of the present invention for solving the above problems is characterized in that it first comprises a composition containing the following (a), (b) and (c) and not containing a substantial amount of a chlorinating solvent. It is said.
(A) Ethylene, propylene, butylene glycol ether ester of the formula I of 95-10 w%
O
‖
R 1 O- (CH 2- CHR 2 O) n- CR 3 (I)
(In the above equation, R 1 is independently a C 1 to C 4 alkyl group and R 2 is independently hydrogen, methyl, and ethyl.
R 3 is independently a C 1 to C 4 alkyl group, n is 1 to 4)
(A) 0 to 30 w% of organic protic solvent (c) 5 to 80 w% of water Secondly, the organic protic solvent is an alcohol having 3 to 18 carbon atoms.
Thirdly, it is characterized by containing a basic or acidic compound.
Fourth, the composition described above is thickened to improve coatability and workability.
【0009】
【発明の実施の形態】
以下本発明の実施形態につき詳述すると、本発明においては外壁等の塗膜並びにプラス
ティックタイルの剥離除去に有効な組成物で下記(ア),(イ),(ウ)を含み、且つ実
質量の塩素化溶剤を含まない組成物で、その剥離除去効率が良く、あらゆる面で安全性の
高い剥離剤及び剥離方法が提供される。
(ア)95〜10w%の下式Iのエチレン、プロピレン、ブチレングリコールエーテルエ
ステル
O
‖
R1O−(CH2−CHR2O)n−C−R3 (I)
(上式中、R1は独立にC1〜C4アルキル基でR2は独立に水素、メチル、エチルであり、
R3は独立にC1〜C4アルキル基であり、nは1〜4である)
(イ)0〜30w%の有機プロトン性溶媒
(ウ)5〜80w%の水
そして好ましくは、エチレン、プロピレン並びにブチレングリコールエーテルエステル
を有効量含有し、不燃化及び適量の溶剤を容易に塗布する為に水を10%以上添加し、水
溶性増粘剤を例えば、天然ポリマー誘導体やポリアクリレートのアルカリ金属塩やアンモ
ニウム塩を用い適当に増粘された剥離剤とする。0009
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, embodiments of the present invention will be described in detail. In the present invention, a composition effective for peeling and removing a coating film such as an outer wall and plastic tiles, which contains the following (a), (b), and (c), and has a substantial amount. A peeling agent and a peeling method which are not chlorinated solvent-free, have good peeling removal efficiency, and are highly safe in all aspects.
(A) Ethylene, propylene, butylene glycol ether ester of the formula I of 95-10 w%
O
‖
R 1 O- (CH 2- CHR 2 O) n- CR 3 (I)
(In the above formula, R 1 R 2 in C 1 -C 4 alkyl Le groups independently are independently hydrogen, methyl, ethyl,
R 3 is independently a C 1 to C 4 alkyl group, n is 1 to 4)
(A) 0 to 30 w% organic protonic solvent (c) 5 to 80 w% water And preferably, an effective amount of ethylene, propylene and butylene glycol ether ester is contained, and a non-combustible and an appropriate amount of solvent is easily applied. Therefore, 10% or more of water is added to prepare a water-soluble thickener, for example, a release agent appropriately thickened by using an alkali metal salt or an ammonium salt of a natural polymer derivative or polyacrylate.
式Iにおいて、R1は独立にC1〜C4アルキル基でR2は独立に水素、メチルもしくはエチルであり、R3は独立にC1 〜C4アルキル基であり、nは1〜4個である。R1並びにR3アルキル基は分枝鎖又は非分枝鎖であってよい。このアルキル基の例は、メチル、エチル、n−プロピル、イソブロピル、n−ブチルもしくはイソブチルである。プロピル及びブチル基のうち、n−プロピル及びn−ブチルが浸透と溶解のバランス上好ましい。式Iの最も好ましいエチレン、プロピレン並びにブチレングリコールエーテルエステルは、R1、R2並びにR3がメチルであるものである。In Formula I, R 1 is an independently C 1 to C 4 alkyl group, R 2 is an independent hydrogen, methyl or ethyl, R 3 is an independent C 1 to C 4 alkyl group, and n is 1 to 4. It is an individual. The R 1 and R 3 alkyl groups may be branched or unbranched. Examples of this alkyl group are methyl, ethyl, n-propyl, isobropil, n-butyl or isobutyl. Of the propyl and butyl groups, n-propyl and n-butyl are preferable in terms of the balance between permeation and dissolution. The most preferred ethylene, propylene and butylene glycol ether esters of Formula I are those in which R 1 , R 2 and R 3 are methyl.
備考1)表中の略号は下記の意味を示す。([表2]においても同じ)
MDPGAC…ジプロピレングリコールモノメチルエーテル
アセテート
DEG …ジエチレングリコール
MDPG …ジプロピレングリコールモノメチルエーテル
NMP …N−メチル−2−ピロリドン
GB …γ−ブチロラクトン
2)試験片の塗料がスクレバーにより剥離除去するに十分な軟らかさになった場合
をすべて「○」で表す。「×」は塗布された本発明の組成物又は塗布された比較
溶剤が十分な効果がないことを意味し、「△」はさらに放置すれば除去可能とな
ることを意味する。又、除去可能なものの除去容易性を5段表示し、5を最良と
する。
Remarks 1) The abbreviations in the table have the following meanings. (The same applies to [Table 2])
MDPGAC ... Dipropylene glycol monomethyl ether
Acetate DEG ... Diethylene glycol MDPG ... Dipropylene glycol Monomethyl ether NMP ... N-Methyl-2-pyrrolidone GB ... γ-Butyrolactone 2) When the paint on the test piece becomes soft enough to be peeled off by the scrubber, "○" Is represented by. “X” means that the applied composition of the present invention or the applied comparative solvent is not sufficiently effective, and “Δ” means that it can be removed if left unattended. In addition, the ease of removal of removable items is displayed in 5 stages, and 5 is the best.
Claims (1)
い組成物からなる外壁等の塗膜並びにプラスティックタイル用剥離剤。
(ア)95〜10w%の下式Iのエチレン、プロピレン、ブチレングリコールエーテルエ
ステル
(上式中、R1は独立にC1〜C4アルキル基でR2は独立に水素、メチル、エチルであり、
R3は独立にC1〜C4アルキル基であり、nは1〜4である)
(イ)0〜30w%の有機プロトン性溶媒
(ウ)5〜80w%の水A release agent for a coating film such as an outer wall and a plastic tile, which comprises the following (a), (b), and (c) and does not contain a substantial amount of a chlorinating solvent.
(A) Ethylene, propylene, butylene glycol ether ester of the formula I of 95-10 w%
(In the above formula, R 1 R 2 in C 1 -C 4 alkyl Le groups independently are independently hydrogen, methyl, ethyl,
R 3 is independently a C 1 to C 4 alkyl group, n is 1 to 4)
(A) 0 to 30 w% organic protic solvent (c) 5 to 80 w% water
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16647098A JP2000001637A (en) | 1998-06-15 | 1998-06-15 | Release agent for coating film of outer wall or the like and plastic tile and peeling |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16647098A JP2000001637A (en) | 1998-06-15 | 1998-06-15 | Release agent for coating film of outer wall or the like and plastic tile and peeling |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000001637A JP2000001637A (en) | 2000-01-07 |
JP2000001637A5 true JP2000001637A5 (en) | 2005-10-20 |
Family
ID=15832000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16647098A Pending JP2000001637A (en) | 1998-06-15 | 1998-06-15 | Release agent for coating film of outer wall or the like and plastic tile and peeling |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2000001637A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4610920B2 (en) * | 2004-03-30 | 2011-01-12 | スイショウ油化工業株式会社 | Release agent composition and method for producing the same |
JP5226213B2 (en) * | 2004-07-14 | 2013-07-03 | 日立マクセル株式会社 | Coating material release agent and coating material release sheet |
WO2006013714A1 (en) * | 2004-07-14 | 2006-02-09 | Sliontec Corporation | Method of stripping coating material |
CN108084815A (en) * | 2017-12-19 | 2018-05-29 | 宁波爱克创威新材料科技有限公司 | A kind of alternating flashing light inner wall decorative coating and preparation method thereof |
-
1998
- 1998-06-15 JP JP16647098A patent/JP2000001637A/en active Pending
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