CA2017090A1 - Coating composition - Google Patents

Coating composition

Info

Publication number
CA2017090A1
CA2017090A1 CA 2017090 CA2017090A CA2017090A1 CA 2017090 A1 CA2017090 A1 CA 2017090A1 CA 2017090 CA2017090 CA 2017090 CA 2017090 A CA2017090 A CA 2017090A CA 2017090 A1 CA2017090 A1 CA 2017090A1
Authority
CA
Canada
Prior art keywords
polysiloxane
composition
composition according
water
emulsified
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.)
Abandoned
Application number
CA 2017090
Other languages
French (fr)
Inventor
Stephen Dunn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CA 2017090 priority Critical patent/CA2017090A1/en
Priority to GB9110046A priority patent/GB2244715B/en
Priority to AU77026/91A priority patent/AU651103B2/en
Priority to DE19914115857 priority patent/DE4115857A1/en
Priority to FR9106349A priority patent/FR2662171A1/en
Publication of CA2017090A1 publication Critical patent/CA2017090A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/46Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
    • C04B41/49Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Organo-clay compounds; Organo-silicates, i.e. ortho- or polysilicic acid esters ; Organo-phosphorus compounds; Organo-inorganic complexes
    • C04B41/4905Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Organo-clay compounds; Organo-silicates, i.e. ortho- or polysilicic acid esters ; Organo-phosphorus compounds; Organo-inorganic complexes containing silicon
    • C04B41/495Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Organo-clay compounds; Organo-silicates, i.e. ortho- or polysilicic acid esters ; Organo-phosphorus compounds; Organo-inorganic complexes containing silicon applied to the substrate as oligomers or polymers
    • C04B41/4961Polyorganosiloxanes, i.e. polymers with a Si-O-Si-O-chain; "silicones"
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/28Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
    • C03C17/30Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with silicon-containing compounds
    • 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
    • C09D183/00Coating 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
    • C09D183/04Polysiloxanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Structural Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)

Abstract

A B S T R A C T

A composition for coating porous and nonporous materials to render same water repellent with a composition consisting essentially of an alkyl polysiloxane and sodium silicate in an amount about 5% to 150% based on weight or volume of said polysiloxane.

Description

- ~ ~? l ;l ~ ~

This invention relates to a method for treating the surface of porous materials such as leather, canvas, fabrics, etc., and nonporous materials such as glass, plastics, metal, ceramics, etc., to make them repel water, to reduce the build-up of grime and dirt, to reduce the bonding of frost and ice and to inhibit the occurrence of rust.

Water can cause great damage to a wide range of materials.
It can reduce effective life, performance and appearance. Water can cause impaired vision, staining, soiling, corrosion and rusting, and can change electrical properties.

The water repellent products that are currently available have many disadvantages. They are often flammable, toxic or corrosive, and often contain acids such as sulphuric or hydrochloric. They are thus dangerous in preparation, transportation, in use.

The present invention provides a nonflammable water repellant product that is noncorrosive, nonabrasive, and nontoxic and does not contain acids or chlorides.

Currently available rain repellent products can be applied to only a few materials, and often they require extensive preparation of the surface to be treated, and special application methods. Current water repellent compositions often lack long life and durability and they often streak and smear.

Compositions containing acids should not be used on aircraft or automobile windshields because of the rubber or other materials used in mounting the windscreens.

It is, therefore, an object of the present invention to provide a novel water repellent composition which can be applied to a wide number of materials, both porous and nonporous, to make them water repellent.

Another objective of this invention is to make an improved water repellent composition which is nonflammable, nontoxic, noncorrosive, nonabrasive, free from acids and chlorides and which will not damage paint, dopes, fabrics, metals, glass, rubber, plastics, ceramics, and so on.

A further objective of the present invention is to make a water repellent composition that is very economical, easy to apply to surfaces of any shape, long-lasting, and durable.

A further object of the present invention is to provide a prcduct that does not materially alter the refractive index of glass or plastic transparencies and is able to resist W
deterioration.

20Still another object of the invention is to provide a composition that will not lose its effectiveness if it is subject to alcohol, de-icing fluids, gasoline, antifreeze, glycols, heat, or cold.

In a broad aspect, the present invention relates to a composition for coating porous and nonporous materials to render same water repellent with a composition consisting essentially of an alkyl polysiloxane having the formula:

o ' sio Wherein n being an integer greater than 1, R, a lower alkyl radical containing from 1 to 7 carbon atoms, and Ra hydrogen, a lower alkyl radical containing from 1 to 7 carbon atoms, or an aryl radical containing about 6 carbon atoms; and sodium silicate in an amount about 5% to 85% based on weight or volume of said polysiloxane.

Polysiloxanes alone have virtually no ability to adhere and to be a durable water repellent product and it is necessary to add an agent so as to have the composition adhere to a surface and to make the surface water repellent. The addition of sodium silicate as described herein accomplishes this.

Not all polysiloxanes are effective. Examples of suitable polysiloxanes are phenylmethylpolysiloxane, polydimethylsiloxane, methylhydrogen polysiloxane. They are available from Dow Corning.

The amount of sodium silicate relative to the above polysiloxanes has a wide range of effectiveness. Ratios from 5%
- 150% sodium silicate by weight or volume, with a preferred range of 40% - 60% sodium silicate to polysiloxane are within the effective ranges of the present invention.

The active ingredients, polysiloxane and sodium silicate, can be used in solution alone but other compounds can be advantageously added.

Moreover, the composition is still effective in diluted form. Dilution is accomplished by adding an emulsifier to a suitable polysiloxane, so that there is a silicone content of 30%
- 70%, and then adding water to make the desired composition.
Dilutions of up to two hundred (200) parts water to one (1) part polysiloxane emulsion are possible.

It is a very important part of this invention that the relatively expensive polysiloxane can be emulsified and then diluted with water without loss of effectiveness. As only a very thin film of the composition should be applied to the material dilution is desired from a technical consideration as well as an economic consideration.
:.
The amount of dilution that is possible has a wide range.
The applicant has successfully tested two hundred parts water to one part emulsified polysiloxane but the preferred amount is forty to sixty (40-60) parts water to one (1) part emulsified polysiloxane.

The composition has been successfully tested over the following ranges:
* 400 parts of emulsified polydimethylsiloxane (30% - 70%
silicone or emulsified phenylmethylpolysiloxane (30% -70% silicone) * 400 - 80,000 parts water * 40 - 600 parts sodium silicate.

The preferred composition is:
* 400 parts of emulsified polydimethylsiloxane (55% - 65%
silicone) or emulsified phenylmethylpolysiloxane) * 18,000 - 22,000 parts water * 180 - 220 parts sodium silicate.
, .
Preparation of the composition is easy and safe. The emulsified polysiloxane and water are thoroughly mixed and then the sodium silicate is added and thoroughly mixed. The materials are mixed at normal room temperature.

:

Examples of suitable formulations follow:

Example 1 1 litre of a suitable polysiloxane was mixed with one-half litre of sodium silicate and 40 litres of water.

Example 2 1 litre of a suitable polysiloxane was mixed with one litre of sodium silicate and 60 litres of water.

Example 3 1 litre of a suitable polysiloxane was mixed with one-fifth litre of sodium silicate and one hundred litres of water.

Example 4 1 litre of a suitable polysiloxane was mixed with one-half litre of sodium silicate and five litres of water. lml of - glycerine (USP) was then added.

Example 5 1 litre of a suitable polysiloxane was mixed with one-half litre of sodium silicate and eighty litres of water. lml of propylene glycol was then added.

-' , ' Example 6 1 litre of a suitable polysiloxane was mixed with three-quarters litre of sodium silicate and one-hundred and twenty litres of water. lml of glycerine (USP) was then added.

~X3~D19_~
1 litre of a suitable polysiloxane was mixed with one-half litre of sodium silicate and 10 litres of water.

Example 8 1 litre of a suitable polysiloxane was used with 1~ litres of sodium silicate and 50 litres of water.

In each of the foregoing examples, the polysiloxane utilized was Dow Corning 346 Silicone Emulsion. The sodium starting silicate solution in each case was an aqueous solution containing 37.6% sodium silicate.

In certain uses it could be desirable to include additional polishing compounds. Adding one (1) part propylene glycol (USP) or one (1) part glycerine (USP) to the above preferred composition adds to polishing characteristics. As a variation of the foregoing one half (%) part propylen~e glycol (USP) plus one half (~) part glycerine (USP) may be adqed. Care must be taken not to add these additional polishing ing~eqte~ts in exce~

of the foregoing as this could cause a smearing effect in application.

The composition should be stored at above freezing temperatures. However, if it freezes it may be thawed at room temperature and there will be no loss of effectiveness.

To apply, one first cleans and dries the surface to be treated. A clean dry cloth is moistened with the composition, which is applied lightly over the entire surface. It is allowed to partially air dry and then buffed. Only a thin film is required. The composition can also be easily applied by brush or spray.

A number of tests, for a wide range of purposes, with the composition has been done. One of the most important uses is to repel rain from windscreens on aircraft, motor vehicles such as automobiles, trucks, boats. All of the glass on the driver's side of an automobile was treated and then driven in moderate to cloudburst rain conditions. The rain on the treated glass formed into innumerable tiny beads that did not coalesce. These tiny beads were blown off the qlass as the speed approached 30 - 40 m.p.h., and the visibility was excellent without the use of the windshield wipers. The untreated glass had the typical water sheeting and impaired to zero visibility. Subsequently, all the glass on two cars was treated and after six months during which time the cars had been washed approximately twice weekly in 2l ~Jv~J ~

typical service station mechanical car washes, windshield wipers were still not required.

Another important feature of the present invention is that - it inhibits the bonding of frost and ice to the treated surface.
This is not to say that it prevents frost and ice from forming on the treated surface, but that it makes it much easier to remove. Several different types of glass, each about one foot square, were coated with the composition and then sprayed with water. They were then placed in a deep freeze for several hours so the water would freeze. When the treated glass was removed from the freezer there were hundreds of tiny frozen beads on the surface which were removed with gentle scraping. The freezing/scraping tests were repeated 47 times without loss of efficiency.

Moreover, the composition of the present invention is useful in coating aircraft wings to render de-icing more efficient.
Also, the composition of the present invention may be used to coat boats and water craft to inhibit ice and dirt build-up. The composition may also be used as a treatment for snow skis, to decrease their friction against snow.

The removal of insect splatter on a windshield that has been treated with the composition is facilitated.

..

The composition can be applied to leather goods such as shoes, coats, belts, etc., to make them water repellent. In addition to the water repellency the leather, especially shoes, takes on a lustre and shine.

The composition was applied to a new steel chisel, a new saw, a new pair of pliers and an iron bar. They were left outside on moist dirt and exposed to the elements. After eight months there was no sign of rust.

The composition was applied to one half of a silver wine cooler. After several weeks there was only a small amount of tarnish on the treated surface whereas the untreated surface had the usual unattractive tarnish build-up.

The composition was applied to a two gallon brass pail and the tarnish build-up has been greatly reduced.

The composition was applied to the plastic water container for a household humidifier system. It has inhibited scaling from the minerals in the water from adhering to the treated surface.
It is thus much easier to clean the humidifier water pan.

The composition was sprayed on the leaves of indoor tropical plants found in homes and offices. The leaves took a very pleasant shine than enhances their appearance. After eight months (at the time of writing) the plants have not shown any deleterious effect and in fact have prospered.

It is to be understood that the examples described above are not meant to limit the scope of the present invention. It is expected that numerous variants will be obvious to the person skilled in the coating composition formulation art, without any departure from the spirit of the present invention. The appended claims, properly construed, form the only limitation upon the scope of the present invention.

Claims (8)

1. A composition for coating porous and nonporous materials to render same water repellent with a composition consisting essentially of an alkyl polysiloxane having the formula:

n n being an integer greater than 1; R1 a lower alkyl radical containing from 1 to 7 carbon atoms; and R2 hydrogen, a lower alkyl radical containing from 1 to 7 carbon atoms, or an aryl radical containing about 6 carbon atoms;

and sodium silicate in an amount about 5% to 150% based on weight or volume of said polysiloxane.
2. A composition according to Claim l wherein said composition further contains a polysiloxane emulsifier so that the emulsified polysiloxane contains 30% - 70% silicone to which is added up to 200 parts water per one part of emulsified polysiloxane.
3. A composition according to Claim 1 wherein said composition further contains one part propylene glycol (USP) or glycerine (USP) per 400 parts of emulsified polysiloxane.
4. A composition according to Claim 1 wherein said composition further contains one half part propylene glycol and one half of one part glycerine (USP) per 400 parts emulsified polysiloxane.
5. A composition according to Claim 1 wherein said alkyl polysiloxane is phenylmethyl polysiloxane.
6. A composition according to Claim 1 wherein said alkyl polysiloxane is methylhydrogen polysiloxane.
7. A composition according to Claim 1 wherein n has a value about 4-950.
8. A composition according to Claim 1 wherein said alkyl polysiloxane is polydimethyl siloxane.

10. A composition according to Claim 1 wherein said composition further contains water as a solvent and diluent.
CA 2017090 1990-05-17 1990-05-17 Coating composition Abandoned CA2017090A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA 2017090 CA2017090A1 (en) 1990-05-17 1990-05-17 Coating composition
GB9110046A GB2244715B (en) 1990-05-17 1991-05-09 Coating composition
AU77026/91A AU651103B2 (en) 1990-05-17 1991-05-15 Polysiloxane coating composition
DE19914115857 DE4115857A1 (en) 1990-05-17 1991-05-15 MIXTURE FOR COATING THE SURFACE OF POROUS AND NON-POROUS MATERIALS
FR9106349A FR2662171A1 (en) 1990-05-17 1991-05-17 WATER REPELLENT COMPOSITION FOR POROUS OR NON - POROUS MATERIALS.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA 2017090 CA2017090A1 (en) 1990-05-17 1990-05-17 Coating composition

Publications (1)

Publication Number Publication Date
CA2017090A1 true CA2017090A1 (en) 1991-11-17

Family

ID=4145014

Family Applications (1)

Application Number Title Priority Date Filing Date
CA 2017090 Abandoned CA2017090A1 (en) 1990-05-17 1990-05-17 Coating composition

Country Status (5)

Country Link
AU (1) AU651103B2 (en)
CA (1) CA2017090A1 (en)
DE (1) DE4115857A1 (en)
FR (1) FR2662171A1 (en)
GB (1) GB2244715B (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3142854A1 (en) * 1981-10-29 1983-05-11 Bayer Ag, 5090 Leverkusen 1-CYCLOPROPYL-6-FLUOR-1,4-DIHYDRO-4-OXO-7-PIPERAZINO-CHINOLINE-3-CARBONIC ACIDS, METHOD FOR THE PRODUCTION THEREOF AND THEIR CONTAINING ANTIBACTERIAL AGENTS
US5607503A (en) * 1993-09-03 1997-03-04 Refract-A-Gard Pty Limited Silica-based binder
DE4419257A1 (en) * 1994-06-01 1995-12-07 Wacker Chemie Gmbh Process for water-repellent impregnation of gypsum
US5685506A (en) * 1995-03-31 1997-11-11 General Electric Company Insect abatement system
FR2782522B1 (en) 1998-08-19 2003-10-03 Atochem Elf Sa WATERPROOFING COMPOSITION
DE10019782A1 (en) * 2000-04-20 2001-10-25 Volkswagen Ag Sensor for cars uses dirt repellent window layers allows wide choice of location at reduced cost
DE60235887D1 (en) * 2001-05-08 2010-05-20 Danish Technological Inst Ener ICE-NUCKING ANTI-SHAFT
DE10260377A1 (en) * 2002-12-16 2004-07-08 Ami Agrolinz Melamine International Gmbh Hydrophobing additive, hydrophobized sheet and a method for hydrophobing

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1069257A (en) * 1962-12-21 1967-05-17 Dunlop Rubber Co Improvements in or relating to wheels
JPS5571767A (en) * 1978-11-21 1980-05-30 Osaka Packing Seizosho:Kk Corrosionproof composition
US4244849A (en) * 1979-08-06 1981-01-13 Dow Corning Corporation Silicone emulsion which provides an elastomeric product and methods for preparation
JPS5650166A (en) * 1979-09-26 1981-05-07 Isao Kiyosue Manufacture of new construction material
US4448919A (en) * 1982-09-30 1984-05-15 Kansai Paint Company Anti-icing compositions
US4433069A (en) * 1983-01-03 1984-02-21 Dow Corning Corporation Method for preparing flame resistant polysiloxane foams and foams prepared thereby
JPS6096650A (en) * 1983-10-31 1985-05-30 Toray Silicone Co Ltd Production of aqueous silicone emulsion composition
JPS6151069A (en) * 1984-08-20 1986-03-13 Kansai Paint Co Ltd Anti-icing paint composition
DE3503957C1 (en) * 1985-02-06 1986-10-09 GfO Gesellschaft für Oberflächentechnik mbH, 7070 Schwäbisch Gmünd Coating agent for anti-reflective coatings and process for its production
FR2621921B1 (en) * 1987-10-20 1990-02-23 Rhone Poulenc Chimie AQUEOUS SILICONE EMULSION WHICH CAN CROSSLINK TO AN ELASTOMER BY REMOVING WATER

Also Published As

Publication number Publication date
FR2662171A1 (en) 1991-11-22
GB2244715B (en) 1994-06-01
DE4115857A1 (en) 1991-11-21
AU651103B2 (en) 1994-07-14
AU7702691A (en) 1991-11-21
GB2244715A (en) 1991-12-11
GB9110046D0 (en) 1991-07-03

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