EP2076154A2 - Zusammensetzungen zur speziellen verwendung als lösungsmittel zur reinigung von lackierarbeiten - Google Patents
Zusammensetzungen zur speziellen verwendung als lösungsmittel zur reinigung von lackierarbeitenInfo
- Publication number
- EP2076154A2 EP2076154A2 EP07858540A EP07858540A EP2076154A2 EP 2076154 A2 EP2076154 A2 EP 2076154A2 EP 07858540 A EP07858540 A EP 07858540A EP 07858540 A EP07858540 A EP 07858540A EP 2076154 A2 EP2076154 A2 EP 2076154A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- compositions
- parts
- solvents
- compositions according
- 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.)
- Withdrawn
Links
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
- C09D9/00—Chemical paint or ink removers
- C09D9/005—Chemical paint or ink removers containing organic solvents
Definitions
- the present invention relates to the field of solvents, and more particularly the solvents used for cleaning paints.
- paint cleaning is intended to mean all the means for removing a partially dried but not totally aged paint or varnish (for example in the case of pickling), for example in the form of:
- chlorinated solvents and hydrocarbons eg white-spirit
- trichlorethylene banned from sale to the general public
- 2 - paraffinic hydrocarbons normal and iso: C8 to C12 content by weight of between 40 and 60%.
- 3 - cycloparaffinic hydrocarbons C9 to C12 content by weight generally close to 30% but up to 70%.
- the classic commercial white spirit contains 17 to 18% aromatics but its benzene content does not exceed the 0.1% limit beyond which the white spirit would be classified as a CMR substance (Carcinogenic / Mutagenic / Reprotoxic). ); the classic white spirit has the following labeling: Xn (harmful) - N (dangerous for the environment) with the risk phrases: R10 R51 / 53 R65 R66 R67
- the present invention relates to novel compositions based on ester (s) of fatty acids and oxygenated solvent (s).
- compositions according to the invention may be partially or completely derived from agromaterials and therefore will not include any labeling of (eco) toxicity, insofar as they are devoid of harmfulness but also flammability.
- compositions according to the invention comprise ⁇ from 10 to 90 parts by weight, and preferably from 30 to 70 parts by weight of at least one fatty acid ester, preferably methyl.
- oxygenated solvents mention may be made of diacetone alcohol (DAA) of formula
- the DAA is labeled Xi, irritating with the risk phrase R36. Mention may also be made of alkyl lactates (methyl, ethyl, propyl, butyl, etc.) or, for example, certain glycol ethers such as diethylene glycol mono-n-butyl ether.
- compositions according to the invention have the advantage of being non-(eco) toxic, non-flammable, of having a low vapor pressure and therefore a slow evaporation rate, a very low odor, while at the same time being effective for the cleaning of paint and varnish equivalent to that of the white spirit.
- compositions according to the invention have a slightly slower evaporation than the white spirit which, in addition to the environmental benefit, avoids the deterioration of the material stained with paints (brushes with glued bristles, unusable rollers, etc.). ) due to too fast drying.
- the fatty acid ester, and the solvent used in the compositions according to the invention are agromaterials.
- agromaterials include:
- DMI dimethylisosorbide
- compositions based on methyl esters of fatty acids derived from castor oil and dimethylisosorbide are particularly preferred by the applicant. These two components are not VOCs (volatile organic compounds) according to Directive 1999/13 / EC of March 11, 1999 which gives the following definition for VOCs: "Any organic compound, with the exception of methane, having a pressure of Steam equal to or greater than 10 Pa at 20 ° C or having a corresponding volatility under particular conditions of use. "
- compositions predominantly based on oxygenated solvent (s) are preferred, and preferably those comprising at least 70 parts by weight of DAA and / or DMI and less than 30 parts by weight. parts by weight of ester (s) of fatty acid.
- the viscosity of the compositions according to the invention also depends on the length of the fatty chain of the fatty acid ester (s): (for example, the coconut methyl ester (mainly based on C12 laurate) has a lower viscosity than that of the Esteral A-type C18 methyl ester Using a shorter fatty chain ester in the composition according to the invention reduces the viscosity of the final composition.
- compositions according to the invention may furthermore contain surfactants, preferably nonionic surfactants, and advantageously surfactants based on agromaterials, for example fatty esters, in particular sucrose fatty esters, with a hydrophilic head. based on sugars and a hydrophobic part consisting of a fatty chain derived from vegetable matter.
- surfactants preferably nonionic surfactants, and advantageously surfactants based on agromaterials, for example fatty esters, in particular sucrose fatty esters, with a hydrophilic head. based on sugars and a hydrophobic part consisting of a fatty chain derived from vegetable matter.
- the compositions according to the invention may further contain compatibilizing agents used as additives for the use of formulations in very high humidity conditions such as dimethylsulfoxide (DMSO) or hexylene glycol.
- DMSO dimethylsulfoxide
- hexylene glycol hexylene glycol
- This composition is tested for the elimination of paints and varnishes on a large number of supports. It is found that it has a good ability to clean these supports, particularly for glycerol, alkyd paints; moreover, it has a higher viscosity than the white spirit.
- composition has a lower evaporation rate than white spirit Example 2
- the measurement of the evaporation rate is based on monitoring the mass of the mixture left in a container over time.
- the initial rates of evaporation are similar for compositions based on Esterol A ® / DAA or white spirit (of the order of 0.025 g / h).
- the ester remains Methyl (Esterai A ® or EMC) which avoids the dry setting of the layering material (advantage over the white spirit).
- Esterai A ® / DMI agrosolvents given the very low vapor pressures, evaporation becomes extremely slow which is sought.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0654242A FR2907128B1 (fr) | 2006-10-12 | 2006-10-12 | Compositions utilisables notamment comme solvants pour le nettoyage de peintures |
PCT/FR2007/052110 WO2008043954A2 (fr) | 2006-10-12 | 2007-10-10 | Compositions utilisables notamment comme solvants pour le nettoyage de peintures |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2076154A2 true EP2076154A2 (de) | 2009-07-08 |
Family
ID=38009235
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07858540A Withdrawn EP2076154A2 (de) | 2006-10-12 | 2007-10-10 | Zusammensetzungen zur speziellen verwendung als lösungsmittel zur reinigung von lackierarbeiten |
Country Status (6)
Country | Link |
---|---|
US (1) | US8299008B2 (de) |
EP (1) | EP2076154A2 (de) |
JP (1) | JP5301447B2 (de) |
CN (1) | CN101583298B (de) |
FR (1) | FR2907128B1 (de) |
WO (1) | WO2008043954A2 (de) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2368971B1 (de) * | 2010-03-18 | 2014-06-18 | DENOLLE, Yann | Verwendung einer Mischung von Fettsäuremethylestern in C16-C20-Rizinusöl mit mindestens einem Glyzerid-Ethoxyl als Reinigungssubstanz |
CN103160161B (zh) * | 2011-12-16 | 2015-06-17 | 天津立昌科技有限公司 | 一种漆膜剥离剂 |
WO2015108874A1 (en) | 2014-01-16 | 2015-07-23 | Elevance Renewable Sciences, Inc. | Olefinic ester compositions and their use in oil- and gas-related applications |
JP2017110173A (ja) * | 2015-12-15 | 2017-06-22 | 実 岡部 | 洗浄剤,消臭剤および抗菌剤ならびに洗浄,消臭または抗菌方法 |
US11873464B2 (en) * | 2021-08-10 | 2024-01-16 | Herman Kron | Paint brush cleaning and gum remover composition comprising isopropylamine alkylbenzenesulfonate |
KR20240049821A (ko) | 2021-08-23 | 2024-04-17 | 바이오버라티브 테라퓨틱스 인크. | 바큘로바이러스 발현 시스템 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0407959A2 (de) * | 1989-07-11 | 1991-01-16 | Lion Corporation | Verfahren zur Herstellung von Polyolfettsäure-Monoestern |
JPH08218010A (ja) * | 1995-02-13 | 1996-08-27 | Neos Co Ltd | 水溶性塗料剥離剤 |
US5824326A (en) * | 1997-06-27 | 1998-10-20 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Activity enhancement of ferulic acid with dimethyl isosorbride in cosmetic compositions |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954648A (en) * | 1969-12-22 | 1976-05-04 | Pennwalt Corporation | Coatings removal composition containing an alkali metal hydroxide, an oxygenated organic solvent, and an amine |
US5258070A (en) * | 1992-07-10 | 1993-11-02 | Charles Monteleone | Nail lacquer remover comprising propylene carbonate, propylene glycol and dimethyl isosorbide |
JPH10330795A (ja) * | 1997-06-03 | 1998-12-15 | Mitsubishi Rayon Co Ltd | エアゾール型スプレー洗浄剤および洗浄方法 |
DE19737071C2 (de) * | 1997-08-26 | 1999-09-09 | Henkel Kgaa | Abbeizmittel |
JPH1192696A (ja) * | 1997-09-22 | 1999-04-06 | Neos Co Ltd | 常温乾燥塗料用水溶性剥離剤 |
US6191087B1 (en) * | 1999-09-03 | 2001-02-20 | Vertec Biosolvents, Llc | Environmentally friendly solvent |
US6284720B1 (en) * | 1999-09-03 | 2001-09-04 | Vertec Biosolvents, Llc | Environmentally friendly ink cleaning preparation |
US6096699A (en) * | 1999-09-03 | 2000-08-01 | Ntec Versol, Llc | Environmentally friendly solvent |
SE516120C2 (sv) * | 2000-03-02 | 2001-11-19 | Stripp Chemicals Ab | Medel för rengöring, såsom borttagning av färg |
CN2423972Y (zh) * | 2000-04-19 | 2001-03-21 | 王建 | 索轨道式墙面喷涂清洗机 |
DE10048797A1 (de) * | 2000-10-02 | 2002-04-18 | Bayer Ag | Wirkstoffhaltige Emulsionen |
-
2006
- 2006-10-12 FR FR0654242A patent/FR2907128B1/fr not_active Expired - Fee Related
-
2007
- 2007-10-10 US US12/444,494 patent/US8299008B2/en not_active Expired - Fee Related
- 2007-10-10 JP JP2009531884A patent/JP5301447B2/ja not_active Expired - Fee Related
- 2007-10-10 WO PCT/FR2007/052110 patent/WO2008043954A2/fr active Application Filing
- 2007-10-10 EP EP07858540A patent/EP2076154A2/de not_active Withdrawn
- 2007-10-10 CN CN2007800378390A patent/CN101583298B/zh not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0407959A2 (de) * | 1989-07-11 | 1991-01-16 | Lion Corporation | Verfahren zur Herstellung von Polyolfettsäure-Monoestern |
JPH08218010A (ja) * | 1995-02-13 | 1996-08-27 | Neos Co Ltd | 水溶性塗料剥離剤 |
US5824326A (en) * | 1997-06-27 | 1998-10-20 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Activity enhancement of ferulic acid with dimethyl isosorbride in cosmetic compositions |
Also Published As
Publication number | Publication date |
---|---|
FR2907128A1 (fr) | 2008-04-18 |
FR2907128B1 (fr) | 2012-08-31 |
WO2008043954A3 (fr) | 2008-05-29 |
CN101583298B (zh) | 2012-03-14 |
US20100137182A1 (en) | 2010-06-03 |
JP2010506024A (ja) | 2010-02-25 |
JP5301447B2 (ja) | 2013-09-25 |
US8299008B2 (en) | 2012-10-30 |
WO2008043954A2 (fr) | 2008-04-17 |
CN101583298A (zh) | 2009-11-18 |
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