AU635852B2 - Composition for paint-removal coatings on substrates - Google Patents

Composition for paint-removal coatings on substrates Download PDF

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Publication number
AU635852B2
AU635852B2 AU80294/91A AU8029491A AU635852B2 AU 635852 B2 AU635852 B2 AU 635852B2 AU 80294/91 A AU80294/91 A AU 80294/91A AU 8029491 A AU8029491 A AU 8029491A AU 635852 B2 AU635852 B2 AU 635852B2
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AU
Australia
Prior art keywords
component
composition according
pbw
hydroxyl
paint
Prior art date
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Ceased
Application number
AU80294/91A
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AU8029491A (en
Inventor
Friedrich Volker Beutelrock
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BEUTELROCK CAROLIN
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BEUTELROCK CAROLIN
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Publication of AU8029491A publication Critical patent/AU8029491A/en
Application granted granted Critical
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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/778Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur silicon
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/06Polyurethanes from polyesters

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Description

S F Ref: 186160 AUSTRAL 8 5 2 PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT
ORIGINAL
0,ee 0 @900 0* @0 0 0 *000 0
S
*0 000 5* *0 Name and Address of Applicant: Actual Inventor(s): Address for Service: Invention Title: Carolin Beutelrock Untertrave 105 2400 Lubeck FEDERAL REPUBLIC OF GERMANY Friedrich Volker Beutelrock Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Composition for Paint-Removal Coatings on Substrates The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845/3 P4004628.1 Nort2.br 1 Composition for Paint-Removal Coatings on Substrates In many towns, particularly in cities, paint sprayings, so-called "graffiti", are appearing to an increasing extent on public and private buildings and also on vehicles, particularly on railways and underground railway carriages. Although, on the one hand, graffiti have developed into an art form of its own and are often desirable for improving the appearance of depressing urban concrete districts, daubs devoid of any art, which are, to be found predominantly in towns as well as social and political words, are on the other hand, to be regarded as fouling the image of the town. To remove such paint sprayings from spray guns, officialdom and house owners have to spend large sums every year in order to bring buildings and railway and underground railway carriages back to their original condition. Not only that, but because of the penetration of the sprayed paint into the surface pores of buildings, irreparable damage often occurs, which can only be removed by expensive coatings which, in turn, considerably harm the visual appearance of a building.
e As a preventative measure against such foulings, wax-based coating agents are known which can be applied, for example, to the lower areas of buildings, which areas are particularly endangered by graffiti. Such coatings are to some extent paint rejecting and can be removed, together with the paint sprayings, by means of steam which S25 softens and dissolves the coating from the substrate. A particular of: disadvantage of such wax-based coating agents is the fact that after removal of the graffiti The coating must be renewed, which is an expensive matter.
The task facing the invention thus consists of obtaining an improved composition for paint-removal coatings on substrates, allowing easier removal of paint sprayings, without requiring subsequent reapplication to the substrate. This task is solved by the composition in accordance with the invention.
The composition of this invention for paint-removal coatings on substrates is characterised in that it contains: -2a) a branched, saturated, hydroxyl group-containing polyester having a hydroxyl number (mg KOH/g solid resin) of 180 to 320, a hydroxyl content, based on the solid resin, of 6 to 10%, and an acid number of 6 maximum; b) at least one polyisocynate; c) a polysiloxane modified polyisocynate; d) a curing catalyst for polyurethane; and e) at least one organic solvent.
From the compositions of the invention polyurethane are formed with the surprising effect of easy removability of paint sprayings, attributable, in particular, to the combination of components a) and The modified polyurethanes arising from the compositions of the invention bond firmly and durably to the substrate. Upon spraying with paint we get a dual effect. On the one hand, the substrate accepts the paint poorly and allows the paint to coagulate to a degree and to flow off the surface, which discourages the sprayer from spraying on such surfaces from the outset. On the other hand, paint sprayings can easily be removed from coating after drying, without, at the same time 20 attacking or removing the coating itself.
S .o The hydroxyl number preferably lies in the range 210 to 290, particularly in the range 240 to 280, the hydroxyl content in the range 7 to 9% and the acid number at 4.5 maximum.
So as to increase the water vapour permeability of the coating, which is of particular importance with bridge and underground constructions which come into contact with ground water, it is preferably that a part of component a) be replaced by a branched, S 30 saturated, hydroxyl group-containing polyester having a hydroxyl number of 120 to less than 180 and a hydroxyl content of 3 to less than 6%, Pe/ Et-h erand/or by a branched, saturated, hydroxyl group-contaiining-proyeate having a hydroxyl content of 8 to 14%. For preference 10 to 50% by wt.
of component a) is replaced by the other polyester or the polyether, special preference being for 20 to 40% by wt. Through the addition of polye-th er such aftolyc:tr with a lower hydroxyl content, or a polyester with a hydroxyl content in the range mentioned, the removability of paint -3sprayings is not adversely affected or only very slightly, while water vapour permeability is considerably increased.
po\yesker- If this addition component is aAe4lm.. e, its hydroxyl number preferably lies at 150 to 170 and its hydroxyl content preferably at 4 to With the polyether, the hydroxyl content is preferably 10 to 12%. Where, in the description and claims, percentages are used in connection with the hydroxyl content, percentages by weight are meant based on the solid content of the respective polyester or polyether.
As component there may be used basically any of the polyisocyanates usual for polyurethanes, especially diisocyanates, but also tri- and tetraisocyanates, or pre-polymers of the same. The polyisocyanates may be of an aromatic, aromatic-aliphatic, aliphatic, or cyclo-aliphatic nature. Since the compositions of the invention are, as a rule, used in the open air, and aromatic polyisocyanates give coatings with a deficient resistance to weathering, it is better to use
O
S* aliphatic polyisocyanates, particularly diisocyanates or their prepolymers, in the compositions of the invention.
When necessary, ordinary blocked polyisocyanates can be considered. These are ordinary commercial compounds, in which, for example, the isocyanate group may be blocked by reaction with an alcohol, with caprolactam, with a phenol or with a glycol. Blocked 25 polyisocyanates thus come into consideration if the compositions of the invention contain components a) to e) together in a uniform mixture.
With unblocked polyisocyanates it is advisable to pack and to store the agent as two components, with component a) contained in one package and components b) and c) in the other.
'Component c) is a polysiloxane modified polyisocyanate and may again be a di-, tri- or tetraisocyanate, but a diisocyanate is preferred and, especially one of an aliphatic nature. This is incorporated into the polyurethane by polymerisation so that the polysiloxane modification is fixed in the polyurethane polymer.
Moisture hardening systems also come up for consideration, which upon i exclusion of moisture are storage stable, and only harden under the 4 effect of atmospheric moisture.
Component d) consists of an ordinary curing catalyst for the preparation of polyurethanes. Such curing catalysts are for example, and in particular tertiary amines, quaternary ammonium salts and ester amines and also different metal compounds, such as zinc octoate or dibutyl tin dilaurate.
The organic solvent is added in sufficient an amount to provide easy handling. The individual components are, in many cases, already contained in a solvent so that such solvents automatically find their way in to the compositions of the invention with the individual components. During storage, in two separate containers, it is best that both of them contain an organic solvent. Basically all organic solvents may be considered which are inert to the polyester components and to the polyisocyanate components. Aromatic substances are preferred, such as xylene, solvent naphtha or the like, and/or esters, 9 such as, butyl acetate, methoxypropyl acetate, ethoxyethyl acetate or ethyglycol acetate, and ketones, such as methylisobutyl ketones or 20 methylethyl ketones.
S A particular favourable paint removing effect is obtained if, in addition to components a) to a polyester modified hydroxy functional polysiloxane is included as component for preference a 25 polyester modified hydroxy functional polydimethyl siloxane. This is best added in an amount of 0.5 to 5, preferably 1 to 3, pbw per 100 pbw of component a).
The compositions of the invention may moreover contain further additives which are usual in coating agents, such as flow agents, pigments, colorants, UV absorbers or the like, provided these materials do not have a detrimental effect on the required properties of the composition.
The optimum composition by weight can be determined by a series of tests. It is advisable that the composition contains, respectively, 100pbw of component 50 to 120, but preferably 60 to 90 pbw of I -o 3 p2 of -ompooennt- Cc)ar. o0,1 +o I bu+ prfe-Febly component 0.5 to 5, but preferably 0.1 to 0.5 pbw of component d).
As a whole, the composition of the invention, independent of whether it is present as a uniform mixture or in two separate containers, preferably contains, respectively, 100 pbw of component 50 to 500, preferably 100 to 250, and better still 140 to 180 pbw of component e).
The compositions of the invention may be applied to the substrates in different ways, such as, for example, by spraying, brushing on, rolling on or in any other usual manner.
Example 1 Component A Strongly branched, saturated, hydroxyl groupcontaining polyester with hydroxyl number (mg KOH/g solid resin) of about 265, a hydroxyl elo content (based on the weight of the solid resin) of about 8% and an acid number (mg KOH/g solid resin) of 4 maximum, as a 004* solution in methoxypropyl pbw S 20 17.63pbw Methoxypropyl pbw Ordinary commercial catalyst for preparation of the 0.13 pbw Flow 0.24 pbw 25 Polyester modified hydroxy functional 1.00 pbw UV 1.00 pbw Component B Prepolymer of aliphatic unmodified diisocyanate 97.00 pbw Polysiloxane modified 3.00 pbw Components A and B were mixed together in the ratio by wt. of 2:1 and applied as a coating to concrete. After curing (hardening) paints were sprayed on from ordinary spray guns. These were poorly accepted by the coating and ran off to some degree. After drying the coatings 6 of paint could easily and completely by removed by the usual cleaning agents.
Example 2 In the formulation of example 1 in component A, 30% by wt. of the 65% solution of the strongly branched, saturated, hydroxyl groupcontaining polyester was replaced by a 75% solution in xylene of a strongly branched, saturated hydroxyl group-containing polyester which was modified by a low molecular fatty acid. This polyester had a hydroxyl of about 165, a hydroxyl content of about 5% and an acid number of about The coatings obtained by this medium were characterised by an increased permeability to water vapour.
Example 3 The formulation of example 1 was repeated wit;h the variation that 20% of the 65% solution of the branched, saturated, hydroxyl groupcontaining polyester was replaced by a branched, saturated, hydroxyl **Goo: group-containing polyester free of solvent, having a hydroxyl content 0 0 of about 11.5% an equivalent weight of about 148, an acid number of less than 0.5 and a density of 200C according to DIN 51757, of 1.03 g1cd.
The composition gave a paint removed coating with about the same paint removing properties as the coatings of examples 1 and 3, but with a water Vapour permeability which was superior to that of example 1

Claims (5)

1. A composition for paint-removal coatings on substrates, characterised in that it contains: a branched, saturated, hydroxy group-containing polyester having a hydroxyl number (mg KOH/g solid resin) of from 180 to 320, a hydroxyl content, based on the solid resin, of 6 to 10% and having an acid number of 6 as the maximum, at least one polyisocynate, a polysiloxane modified polyisocynate, a polyurethane curing catalyst, and at least one organic solvent.
2. A composition according to claim 1, in that it contains, as a partial replacement of component a corresponding amount of a branched, saturated, hydroxyl group-containing polyester having a hydroxyl number of 120 to less than 180 and a hydroxyl content of 3 to less than 6% and/or a branched, saturated hydroxyl group-containing polyether having a hydroxyl content of 8 to 14%.
3. A composition according to claim 2 in that from 10 to 50% by wt of component is replaced.
4. A composition according to claim 2 or claim 3 in that the hydroxyl group-containing polyester has a hydroxyl number of from 150 to
170. ::th 5. A composition according to any one of claims 2 to 4 in that the hydroxyl group-containing polyester has a hydroxyl content of from 4 25 to 6. A composition according to any one of claims 2 to 5 in that the hydroxyl group-containing polyether has a hydroxyl content of from to 12%. 7. A composition according to any one of claims 1 to 6, 30 characterised in that it contains, in addition, a polyester modified hydroxy functional polysiloxane. 8. A composition according to claim 7 characterised In that the polysiloxane is polydlmethylsiloxane. 9. A composition according to any one of claims 1 to 8, characterised In that it contains, in addition, a flow agent. 8 A composition according to any one of claims 1 to 9 characterised in that it contains, as component a branched, saturated, hydroxyl group-containing polyester having a hydroxyl number of from 210 to 290, a hydroxyl content of 7 to 9% and an acid number of 4.5 maximum. 11. A composition according to claim 10 characterised in that the hydroxyl number is from 240 to 280. 12. A composition according to any one of claims 1 to 11 characterised in that it contains, respectively, 100 pbw of component 50 to 120 pbw of component 0.5 to 5 pbw of component and 0.01 to 1 pbw of component 13. A composition according to claim 12 characterised in that it contains 60 to 90 pbw of component 14. A composition according to claim 12 or claim 13 characterised in that it contains 1 to 3 pbw of component A composition according to any one of claims 12 to 14 characterised in that it contains 0.1 to 0.5 pbw of component 16. A composition according to any one of claims 1 to characterised in that it contains 100 pbw of component and 100 to 250 pbw of component 17. A composition accordiHg to claim 16 characterised in that it contains 140 to 180 pbw of component S18. A composition according to any one of claims 7 to 17 characterised in that it contains, respectively, 100 pbw of component (a) 25 and 0.5 to 5 pbw of component 19. A composition according to claim 18 characterised in that it contains 1 to 3 pbw of component 20, A composition for paint-removal coatings on substrates substantially as hereinbefore described with reference to any one of the 30 Examples. S DATED this NINTH day of DECEMBER 1992 Carolin Beutelrock Patent Attorneys for the Applicant SPRUSbN FERGUSON 2326U/jj ABSTRACT Composition for Paint-Removal Coatings on Substrates Compositions for paint-removal coatings on substrates which provide easy removal of paint, without their having to be applied again afterwards, are characterised in that they contain: a) a branched, saturated, hydroxy group-containing polyester having a hydroxyl number (mg KOH/g solid resin) of from 180 to 320, a hydroxyl content, based on the solid resin, of 6 to 10%, and an acid number of 6 as the maximum, b) at least one polyisocynate, c) a polysiloxane modified polyisocynate, d) a polyurethane curing catalyst, and e) at least one organic solvent. b 4
AU80294/91A 1990-02-15 1991-07-09 Composition for paint-removal coatings on substrates Ceased AU635852B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19904004628 DE4004628A1 (en) 1990-02-15 1990-02-15 MEDIUM FOR PAINT-REPELLENT COATING OF SUBSTRATES

Publications (2)

Publication Number Publication Date
AU8029491A AU8029491A (en) 1993-01-14
AU635852B2 true AU635852B2 (en) 1993-04-01

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AU80294/91A Ceased AU635852B2 (en) 1990-02-15 1991-07-09 Composition for paint-removal coatings on substrates

Country Status (5)

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EP (1) EP0442272A3 (en)
JP (1) JPH04356572A (en)
AU (1) AU635852B2 (en)
DE (1) DE4004628A1 (en)
PT (1) PT96765A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103910853A (en) * 2012-12-31 2014-07-09 陶氏环球技术有限公司 Siloxane-carbamate group fouling-release coating

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0808881B1 (en) * 1996-05-23 1999-09-22 Ewald Dörken Ag Coating from a powder paint having an antisticking effect and process for its preparation

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3376657D1 (en) * 1982-08-04 1988-06-23 Dow Corning Siloxane polyester compositions and use thereof
DE3535283A1 (en) * 1985-10-03 1987-04-09 Byk Chemie Gmbh POLYSILOXANES CONTAINING POLYESTER GROUPS FOR VARNISHES AND MOLDS AND THE USE THEREOF
JPS63277222A (en) * 1987-02-16 1988-11-15 Sanyo Chem Ind Ltd Curing resin
CA2005546A1 (en) * 1988-12-14 1990-06-14 Kenneth R. Strudwick Silicone modified polyurethanes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103910853A (en) * 2012-12-31 2014-07-09 陶氏环球技术有限公司 Siloxane-carbamate group fouling-release coating
CN103910853B (en) * 2012-12-31 2016-05-18 陶氏环球技术有限公司 The stained desorption coating of siloxanes-carbamate groups

Also Published As

Publication number Publication date
DE4004628A1 (en) 1991-08-22
PT96765A (en) 1991-10-31
EP0442272A2 (en) 1991-08-21
JPH04356572A (en) 1992-12-10
EP0442272A3 (en) 1992-03-18
AU8029491A (en) 1993-01-14

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