CA2166335A1 - Water soluble pyrolytic paint - Google Patents
Water soluble pyrolytic paintInfo
- Publication number
- CA2166335A1 CA2166335A1 CA002166335A CA2166335A CA2166335A1 CA 2166335 A1 CA2166335 A1 CA 2166335A1 CA 002166335 A CA002166335 A CA 002166335A CA 2166335 A CA2166335 A CA 2166335A CA 2166335 A1 CA2166335 A1 CA 2166335A1
- Authority
- CA
- Canada
- Prior art keywords
- metal
- paint
- water soluble
- boride
- pyrolytic
- 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
Links
- 239000003973 paint Substances 0.000 title claims abstract description 97
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 34
- 229910052751 metal Inorganic materials 0.000 claims abstract description 77
- 239000002184 metal Substances 0.000 claims abstract description 77
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 21
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 150000004767 nitrides Chemical class 0.000 claims abstract description 14
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims abstract description 14
- 239000001509 sodium citrate Substances 0.000 claims abstract description 14
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 13
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 13
- 239000000758 substrate Substances 0.000 claims abstract description 12
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 11
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims abstract description 11
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 11
- 239000000654 additive Substances 0.000 claims abstract description 10
- 230000000996 additive effect Effects 0.000 claims abstract description 10
- 239000002904 solvent Substances 0.000 claims abstract description 8
- 230000003014 reinforcing effect Effects 0.000 claims description 10
- 229910021332 silicide Inorganic materials 0.000 claims description 9
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 claims description 9
- LYCAIKOWRPUZTN-NMQOAUCRSA-N 1,2-dideuteriooxyethane Chemical compound [2H]OCCO[2H] LYCAIKOWRPUZTN-NMQOAUCRSA-N 0.000 claims description 7
- 150000002739 metals Chemical class 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 claims description 5
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 5
- 229910052721 tungsten Inorganic materials 0.000 claims description 5
- 239000010937 tungsten Substances 0.000 claims description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 3
- LGLOITKZTDVGOE-UHFFFAOYSA-N boranylidynemolybdenum Chemical compound [Mo]#B LGLOITKZTDVGOE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 3
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 claims description 3
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 claims description 3
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 3
- 229910052580 B4C Inorganic materials 0.000 claims description 2
- YXTPWUNVHCYOSP-UHFFFAOYSA-N bis($l^{2}-silanylidene)molybdenum Chemical compound [Si]=[Mo]=[Si] YXTPWUNVHCYOSP-UHFFFAOYSA-N 0.000 claims description 2
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 claims description 2
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 claims description 2
- 229910021343 molybdenum disilicide Inorganic materials 0.000 claims description 2
- 229910003470 tongbaite Inorganic materials 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- AUVPWTYQZMLSKY-UHFFFAOYSA-N boron;vanadium Chemical compound [V]#B AUVPWTYQZMLSKY-UHFFFAOYSA-N 0.000 claims 1
- 150000001247 metal acetylides Chemical class 0.000 claims 1
- 239000010936 titanium Substances 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 18
- 239000000377 silicon dioxide Substances 0.000 abstract description 9
- 239000002923 metal particle Substances 0.000 abstract description 8
- 238000002156 mixing Methods 0.000 abstract description 7
- 238000003756 stirring Methods 0.000 abstract description 4
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 abstract description 3
- 238000006482 condensation reaction Methods 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 33
- 238000010422 painting Methods 0.000 description 9
- 239000000470 constituent Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
- 229910052618 mica group Inorganic materials 0.000 description 5
- MHPGUDLSTATOHA-UHFFFAOYSA-N [Si]([O-])([O-])([O-])O[Si]([O-])([O-])[O-].[Mo+6] Chemical compound [Si]([O-])([O-])([O-])O[Si]([O-])([O-])[O-].[Mo+6] MHPGUDLSTATOHA-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000020169 heat generation Effects 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- XMIJDTGORVPYLW-UHFFFAOYSA-N [SiH2] Chemical compound [SiH2] XMIJDTGORVPYLW-UHFFFAOYSA-N 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 238000007592 spray painting technique Methods 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- -1 hydroxyl group ions Chemical class 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- XJKVPKYVPCWHFO-UHFFFAOYSA-N silicon;hydrate Chemical compound O.[Si] XJKVPKYVPCWHFO-UHFFFAOYSA-N 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/28—Nitrogen-containing compounds
-
- 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
- C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
-
- 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
- C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
- C09D1/02—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances alkali metal silicates
- C09D1/04—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances alkali metal silicates with organic additives
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
- C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
- C09D5/084—Inorganic compounds
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
Abstract
The present invention provides a water soluble, inorganic pyrolytic paint which, when dried to form a paint layer, generates heat from a whole surface of the paint layer by supplying electric current therethrough. The pyrolytic paint is prepared by mixing and stirring a mixture of metal carbide, metal oxide, metal nitride, metal boride and metal disilicide and/or additive metal and a solvent containing sodium citrate, ethylene glycol, silicic acid anhydride and/or sodium silicate and water. When painted on a substrate surface and dried, silicon dioxide component thereof forms insoluble macromolecular lands L by condensation reaction of silanol base which form a stable paint layer and metal particles M
thereof bridge the lands L and supported thereby to provide uniform electric resistance throughout a surface of the paint layer, so that the paint layer generate heat uniformly throughout the paint layer by supplying electric current therethrough.
thereof bridge the lands L and supported thereby to provide uniform electric resistance throughout a surface of the paint layer, so that the paint layer generate heat uniformly throughout the paint layer by supplying electric current therethrough.
Description
WATER SOLUBLE PYROLYTIC PAINT
Technical Field:
The present invention relates to a pyrolytic paint which paints a substrate and generates heat by a current flowing therethrough.
Background Art:
Japanese Patent Publication Nos. S49-28695 and S54-37707 propose pyrolytic paints which are organic, water soluble, electrically conductive paints consisting of ionomer resin or its water emulsion containing electrically conductive carbon black.
Since, however, these paints employ organic materials, they can be utilized only at a low temperature of 100C or lower and can not be utilized to generate heat to a middle temperature from 200C to 400C or higher.
An object of the present invention is to provide a water soluble inorganic pyrolytic paint capable of generating heat to a low temperature as well as middle temperature or higher.
Another object of the present invention is to provide a water soluble pyrolytic paint capable of painting various substrates such as ceramics, metal, wood and paper, etc., by suitable means including printing means such as gravure printing, screen printing or painting means such as spray painting, immersion painting.
Summary of the Invention:
A water soluble pyrolytic paint according to the present invention is formed by adding a solvent consisting of sodium citrate, ethylene glycol, silicic acid anhydride and/or sodium silicate and water to a mixture of metal carbide, metal oxide, metal nitride, metal boride and metal silicide and/or an additive metal and agitating them.
The water soluble pyrolytic paint according to the present invention can be regulated such that a coating layer of the paint contains 15-45 wt% metal carbide, 3-15 wt% metal oxide, 0.5-5 wt% metal nitride, 10-30 w% metal boride, 0.5-25 wt% metal cilicide, 10-25 wt% additive metal, 2-3 wt% sodium citrate, 2-2.5 wt% ethylene glycol and 5-10 wt% silicic acid anhydride and/or sodium silicate.
Further, the water soluble pyrolytic paint according to the present invention can be used as a heat generator for heating to a low and middle temperature or a high temperature by changing percentage of the respective constituents of the mixture contained in the coating layer.
The water soluble pyrolytic paint according to the present invention becomes a liquid having desired viscosity and desired thixotropy by mixing the mixture containing metal components with the solvent and agitating them. In such case, the various metals in the mixture form a kind of metal complex together with sodium citrate and ethylene glycol. On the other hand, silanol base of silicon dioxide contained in the mixture and the solvent are sequentially dehydrated and condensed when the paint on a desired, electrically non-conductive substrate is dried and fix the metal particles to a surface of the substrate.
This phenomenon can be considered as similar to random adhesion of sodium ions, hydroxyl group ions and water to siloxynesilanol surface, as shown by the following chemical formula:
_ Si - O- + H20~ Si - OH + OH-2- - Si - H -~ - Si - O - Si - + H20 As illustrated in Fig. 1, silicon dioxide component forms a stable paint layer in the form of non-soluble lands L of macromlecules resulting from condensation reaction of silanol base on a surface S of the substrate which may be of ceramics, metal, wood or paper. The paint layer is strongly and reliably adhered to the surface S even when the latter is flat and smooth.
An outer appearance of the paint layer thus formed, dehydrated and condensed depends upon configuration of various metal particles M, particle sizes and contents thereof and the ~ _ various metal particles M bridge between the lands L.
However, for the paint layer as the whole, the various metal particles M bridge the lands L in a dispersed form. This is realized by forming complexes in the stirring step of the metal mixture in a powder form, adding silicon dioxide and water to the stirred metal mixture and sufficiently mixing and agitating them.
The metal particles bridging the lands L and thus supported by the lands L have a uniform electrical resistance throughout the paint layer and generate heat when an Electric current flows therethrough. Temperature of the paint layer resulting from the heat generation depends upon constituents of the metal particle, ratios of them, configuration of them and densities of them, etc.
In another example of the water soluble pyrolytic paint according to the present invention, the paint layer dehydrated is further painted by a reinforcing paint of perhydropolysilazane or the like. With such reinforcing paint layer, glass particles G fill spaces between the lands L of the paint layer as illustrated in Fig. 2 to fix the metal particles M to the surface S of the substrate more strongly to thereby improve layer strength as well as thermal stability, electrical insulation and chemical resistance of the paint layer.
Further, the water soluble pyrolytic paint and the reinforcing paint can be heat-cured at a relatively low temperature to enhance dehydration and condensation thereof.
The transforming scheme by means of the reinforcing layer of perhydropolysilazane in air is formed by a glass film, that is, a ceramic film containing silicon dioxide as shown by the following chemical formula:
( SiH2 - NH-) + 2-~ SiO2 + NH3 ( SiH2 - NH-) + 2H20--~SiO2 + NH3 + 2H2 Brief Description of the Drawings Fig. 1 illustrates a structure of a paint layer formed by a pyrolytic paint according to the present invention;
Fig. 2 illustrates a structure of the paint layer shown in Fig. 1 with a reinforcing paint layer; and Fig. 3 is a front view of a test sample used in experiments of the present invention.
Detailed Description of the Preferred Embodiments Pyrolytic paints 1 to 4 having different constituents were prepared by mixing solvents containing sodium citrate, ethylene glycol, sodium silicate and water at different mixing rates with mixtures of titanium carbide, titanium oxide, aluminum nitride, chromium boride, molybdenum disilicide, tungsten and nickel at different mixing rates and stirring them.
Test samples of the pyrolytic paints 1 to 4 were painted on surfaces of composite mica plates (lOOmm X lOOmm X l.Omm) composed of natural mica and silicon and dried at 120C + 6C
such that the paints are heat-cured at a relatively low temperature, resulting in paint layers having thickness of 30 to 50 ~m. The constituents of these paint layers were as shown in Table 1 below:
Table 1 Constituent of paint Paint No. 1 No. 2 No. 3 No. 4 titanium carbide 16 wt~ 24 wt%34 wt%43 wt%
titanium oxide 10 wt% 7 wt%5 wt% 3 wt%
aluminum nitride 4 wt% 3.5wt%0.8wt%0.5wt%
chromium boride 15 wt% 17 wt%22 wt%20 wt%
molybdenum disilicate 21 wt% 18 wt%7 wt% 1 wt%
tungsten 9 wt% 10 wt%6 wt% 6 wt%
nickel 5 wt%9 wt% 12 wt% 11 wt%
sodium citrate 3 wt%2 wt% 3 wt% 2 wt%
ethylene glycol 2 wt%2.5wt% 2 wt% 2 wt%
sodium silicate 10 wt%6 wt% 5 wt% 9 wt%
water remnantremnant remnant remnant Each mica plate 1 was provided with electrodes 2 and 3 each 5 mm wide on opposite sides thereof and a power source 4 (DC 12V, 3A: AC 50V, 3A: AClOOV, 3A) was connected between the electrodes as shown in Fig. 3. Surface temperature was measured at a center point 6a and four points 6b to 6e located at 20 mm from an upper and lower edge of the plate and 25 mm from the left and right sides of the plate by using temperature measuring probes.
Table 2 shows maximum temperature and current supply time during which temperature of the paint layer on each plate increases from room temperature to the maximum temperature Tmax (C).
From this, it has been found that the temperature increase of each paint layer with respect to current supply time t (sec) varies in series or linearly. Further, it has been found that temperature at the measuring points increases substantially simultaneously with difference in maximum temperature Tmax between these measuring points being 0.1C or less. From these facts, it has been found that the paint layer generates heat uniformly.
Table 2 Paint No. 1 No. 2 No. 3 No. 4 DC12V Tmax ~C) 121C 218C 342C 402C
(3A) t (sec) 54 sec. 55 sec. 60 sec. 62 sec.
DC50V Tmax (C) 120~C 218C 343C 403C
(3A) t (sec) 25 sec. 30 sec. 36 sec. 40 sec.
(3A) t (sec) L0 sec. ~sCec 3~1sCec ~3C
[Experimental Example 2]
In the similar manner to the Experimental Example 1, composite mica plates were painted with pyrolytive paints 5 to 8 obtained by mixing and stirring a mixture of tungsten carbide, zirconium oxide, aluminum nitride, molybdenum boride, molybdenum disilicate and tungsten and a solvent containing sodium citrate, ethylene glycol, silicic acid anhydride and water and the paints on the mica plates were dried at 120C +
6C, resulting in paint layers having constituents shown in Table 3.
Table 3 Constituent of paint Paint No. 1 No. 2 NQ. 3 No. 4 tungsten carbide 18 wt% 26 wt% 33 wt% 42 wt%
zirconium oxide 12 wt% 13 wt% 4 wt% 3 wt%
aluminum nitride 5 wt% 3 wt% 0.6wt% 0.7wt%
molybdenum boride 11 wt% 14 wt% 26 wt% 16 wt%
molybdenum disilicate 21 wt%13 wt% 4 wt% 3 wt%
tungsten 14 wt% 16 wt% 20 wt% 21 wt%
sodium citrate 3 wt% 3 wt% 2 wt% 2 wt%
ethylene glycol 2 wt% 2 wt% 2 wt% 2 wt%
silicic acid anhydride 9 wt%7 wt% 6 wt% 8 wt%
water remnant remnant remnant remnant Maximum temperature Tmax (oC) of the paint layers and current supply time t (sec) were measured in the similar manner to that in the Experimental Example 1. The result of the measurement is shown in Table 4.
Table 4 Paint No. 5 No. 6 No. 7 No. 8 DC12V Tmax (C) 133C 224C 347C 401C
(3A) t (sec) 58 sec. 65 sec. 58 sec. 62 sec.
DC50V Tmax (C) 136C 223C 347C 401C
(3A) t (sec) 32 sec. 36 sec. 41 sec. 42 sec.
DClOOV Tmax (C) 135C 226C 348C 401C
(3A) t (sec) 15 sec. 19 sec. 20 sec. 20 sec.
The temperature increasing rate and the temperature distribution were similar to those in the Experimental Example 1.
Although details are omitted for simplicity of description, it has been found that pyrolytic paint for low and middle temperature range preferably contains metal carbide 15 to 30 wt%, metal oxide 5 to 10 wt%, metal nitride 3 to 5 wt%, metal boride 10 to 15 wt%, metal silicide 10 to 25 wt%, additive metal 10 to 20 wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5 wt% and silicic acid anhydride and/or sodium silicate 5 to 10 wt%. Further, it has been found that pyrolytic paint for high temperature range preferably contains metal carbide 25 to 45 wt%, metal oxide 3 to 5 wt%, metal nitride 0.5 to 1 wt%, metal boride 15 to 30 wt%, metal silicide 0.5 to 10 wt%, additive metal 15 to 25 wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5 wt% and silicic acid anhydride and/or sodium silicate 5 to 10 wt%.
Other metal carbide than those mentioned in the Experimental Examples 1 and 2 may include boron carbide, chromium carbide, etc. Similarly, other metal oxide may include cellium oxide, aluminum oxide, etc., and other metal boride may include titanium boride, etc. Further, it should be noted that the present invention is not limited to the metal mixture of single metal carbide, single metal oxide, single metal nitride and single metal boride. That is, a plural kinds of metal carbide, etc., may be included in the mixture.
[Experimental Example 3]
On the paint layer of any of pyrolytic paints of the Experimental Examples 1 and 2, a reinforcing coating of perhydropolysilazane is formed by painting and the coating was dried at 120C + 6C so that the latter is heat cured at relatively low temperature. It is preferable in order to prevent clacks from occurring after the drying step that the silicon dioxide ceramic coating of perhydropolysilazane is painted on the paint layer to a thickness of in the order of 3~m.
The paint layer strength, the thermal stability, the electric insulation and the chemical resistance of the paint layer having the reinforcing coating were measured and summarized below:
Strength of Paint layer: Pencil Hardness 9H (MV Hardness 600) Thermal Stability : Maximum Durable Temperature Heat Cycle: Durable in -40C
to 400C
Electric Insulation : 101Q /square cm 216633~
Chemical Resistance : 1000 A/min.
(Conc.: hydrofluolic acid 1 +
nitric acid 99) As described, the pyrolytic paint according to the present invention can generate heat enough to make temperature of the paint as high as 400 C or more which is about 4 or more times the maximum temperature achievable by the known pyrolytic paint, with superior temperature rising characteristics. Further, the heat generation in the present pyrolytic paint layer is uniform throughout the surface of the paint layer.
Further, since the silicon dioxide component adheres to a painting surface while forming the lands, it is possible to form a paint layer strongly adhered to a surface of a substrate which may be of ceramics, metal, wood or paper.
Since, therefore, it is possible to reliably paint a flat and smooth surface. Further, since the present pyrolytic paint is water-soluble, inorganic paint, any substrate surface can be painted by any of the printing means such as gravure printing or screen printing, etc., and painting means such as brush painting, spray painting or immersion painting, etc., even if the substrate surface has a three-dimensional configuration.
Further, there is no generation of undesired gas in the drying step after the painting and thus there is no environmental pollution problem.
In the pyrolytic paint according to the present invention, electric power supplied thereto is not lost as optical energy and heat generation from the ceramics component is performed by radiation of far-infrared ray. Thus, substantially the whole electric power supplied can be converted into thermal energy which can be derived very efficiently.
In addition, by forming the reinforcing layer on the paint layer, the mechanical strength, the thermal stability, the electric insulation and the chemical resistance of the paint layer can be improved remarkably.
Technical Field:
The present invention relates to a pyrolytic paint which paints a substrate and generates heat by a current flowing therethrough.
Background Art:
Japanese Patent Publication Nos. S49-28695 and S54-37707 propose pyrolytic paints which are organic, water soluble, electrically conductive paints consisting of ionomer resin or its water emulsion containing electrically conductive carbon black.
Since, however, these paints employ organic materials, they can be utilized only at a low temperature of 100C or lower and can not be utilized to generate heat to a middle temperature from 200C to 400C or higher.
An object of the present invention is to provide a water soluble inorganic pyrolytic paint capable of generating heat to a low temperature as well as middle temperature or higher.
Another object of the present invention is to provide a water soluble pyrolytic paint capable of painting various substrates such as ceramics, metal, wood and paper, etc., by suitable means including printing means such as gravure printing, screen printing or painting means such as spray painting, immersion painting.
Summary of the Invention:
A water soluble pyrolytic paint according to the present invention is formed by adding a solvent consisting of sodium citrate, ethylene glycol, silicic acid anhydride and/or sodium silicate and water to a mixture of metal carbide, metal oxide, metal nitride, metal boride and metal silicide and/or an additive metal and agitating them.
The water soluble pyrolytic paint according to the present invention can be regulated such that a coating layer of the paint contains 15-45 wt% metal carbide, 3-15 wt% metal oxide, 0.5-5 wt% metal nitride, 10-30 w% metal boride, 0.5-25 wt% metal cilicide, 10-25 wt% additive metal, 2-3 wt% sodium citrate, 2-2.5 wt% ethylene glycol and 5-10 wt% silicic acid anhydride and/or sodium silicate.
Further, the water soluble pyrolytic paint according to the present invention can be used as a heat generator for heating to a low and middle temperature or a high temperature by changing percentage of the respective constituents of the mixture contained in the coating layer.
The water soluble pyrolytic paint according to the present invention becomes a liquid having desired viscosity and desired thixotropy by mixing the mixture containing metal components with the solvent and agitating them. In such case, the various metals in the mixture form a kind of metal complex together with sodium citrate and ethylene glycol. On the other hand, silanol base of silicon dioxide contained in the mixture and the solvent are sequentially dehydrated and condensed when the paint on a desired, electrically non-conductive substrate is dried and fix the metal particles to a surface of the substrate.
This phenomenon can be considered as similar to random adhesion of sodium ions, hydroxyl group ions and water to siloxynesilanol surface, as shown by the following chemical formula:
_ Si - O- + H20~ Si - OH + OH-2- - Si - H -~ - Si - O - Si - + H20 As illustrated in Fig. 1, silicon dioxide component forms a stable paint layer in the form of non-soluble lands L of macromlecules resulting from condensation reaction of silanol base on a surface S of the substrate which may be of ceramics, metal, wood or paper. The paint layer is strongly and reliably adhered to the surface S even when the latter is flat and smooth.
An outer appearance of the paint layer thus formed, dehydrated and condensed depends upon configuration of various metal particles M, particle sizes and contents thereof and the ~ _ various metal particles M bridge between the lands L.
However, for the paint layer as the whole, the various metal particles M bridge the lands L in a dispersed form. This is realized by forming complexes in the stirring step of the metal mixture in a powder form, adding silicon dioxide and water to the stirred metal mixture and sufficiently mixing and agitating them.
The metal particles bridging the lands L and thus supported by the lands L have a uniform electrical resistance throughout the paint layer and generate heat when an Electric current flows therethrough. Temperature of the paint layer resulting from the heat generation depends upon constituents of the metal particle, ratios of them, configuration of them and densities of them, etc.
In another example of the water soluble pyrolytic paint according to the present invention, the paint layer dehydrated is further painted by a reinforcing paint of perhydropolysilazane or the like. With such reinforcing paint layer, glass particles G fill spaces between the lands L of the paint layer as illustrated in Fig. 2 to fix the metal particles M to the surface S of the substrate more strongly to thereby improve layer strength as well as thermal stability, electrical insulation and chemical resistance of the paint layer.
Further, the water soluble pyrolytic paint and the reinforcing paint can be heat-cured at a relatively low temperature to enhance dehydration and condensation thereof.
The transforming scheme by means of the reinforcing layer of perhydropolysilazane in air is formed by a glass film, that is, a ceramic film containing silicon dioxide as shown by the following chemical formula:
( SiH2 - NH-) + 2-~ SiO2 + NH3 ( SiH2 - NH-) + 2H20--~SiO2 + NH3 + 2H2 Brief Description of the Drawings Fig. 1 illustrates a structure of a paint layer formed by a pyrolytic paint according to the present invention;
Fig. 2 illustrates a structure of the paint layer shown in Fig. 1 with a reinforcing paint layer; and Fig. 3 is a front view of a test sample used in experiments of the present invention.
Detailed Description of the Preferred Embodiments Pyrolytic paints 1 to 4 having different constituents were prepared by mixing solvents containing sodium citrate, ethylene glycol, sodium silicate and water at different mixing rates with mixtures of titanium carbide, titanium oxide, aluminum nitride, chromium boride, molybdenum disilicide, tungsten and nickel at different mixing rates and stirring them.
Test samples of the pyrolytic paints 1 to 4 were painted on surfaces of composite mica plates (lOOmm X lOOmm X l.Omm) composed of natural mica and silicon and dried at 120C + 6C
such that the paints are heat-cured at a relatively low temperature, resulting in paint layers having thickness of 30 to 50 ~m. The constituents of these paint layers were as shown in Table 1 below:
Table 1 Constituent of paint Paint No. 1 No. 2 No. 3 No. 4 titanium carbide 16 wt~ 24 wt%34 wt%43 wt%
titanium oxide 10 wt% 7 wt%5 wt% 3 wt%
aluminum nitride 4 wt% 3.5wt%0.8wt%0.5wt%
chromium boride 15 wt% 17 wt%22 wt%20 wt%
molybdenum disilicate 21 wt% 18 wt%7 wt% 1 wt%
tungsten 9 wt% 10 wt%6 wt% 6 wt%
nickel 5 wt%9 wt% 12 wt% 11 wt%
sodium citrate 3 wt%2 wt% 3 wt% 2 wt%
ethylene glycol 2 wt%2.5wt% 2 wt% 2 wt%
sodium silicate 10 wt%6 wt% 5 wt% 9 wt%
water remnantremnant remnant remnant Each mica plate 1 was provided with electrodes 2 and 3 each 5 mm wide on opposite sides thereof and a power source 4 (DC 12V, 3A: AC 50V, 3A: AClOOV, 3A) was connected between the electrodes as shown in Fig. 3. Surface temperature was measured at a center point 6a and four points 6b to 6e located at 20 mm from an upper and lower edge of the plate and 25 mm from the left and right sides of the plate by using temperature measuring probes.
Table 2 shows maximum temperature and current supply time during which temperature of the paint layer on each plate increases from room temperature to the maximum temperature Tmax (C).
From this, it has been found that the temperature increase of each paint layer with respect to current supply time t (sec) varies in series or linearly. Further, it has been found that temperature at the measuring points increases substantially simultaneously with difference in maximum temperature Tmax between these measuring points being 0.1C or less. From these facts, it has been found that the paint layer generates heat uniformly.
Table 2 Paint No. 1 No. 2 No. 3 No. 4 DC12V Tmax ~C) 121C 218C 342C 402C
(3A) t (sec) 54 sec. 55 sec. 60 sec. 62 sec.
DC50V Tmax (C) 120~C 218C 343C 403C
(3A) t (sec) 25 sec. 30 sec. 36 sec. 40 sec.
(3A) t (sec) L0 sec. ~sCec 3~1sCec ~3C
[Experimental Example 2]
In the similar manner to the Experimental Example 1, composite mica plates were painted with pyrolytive paints 5 to 8 obtained by mixing and stirring a mixture of tungsten carbide, zirconium oxide, aluminum nitride, molybdenum boride, molybdenum disilicate and tungsten and a solvent containing sodium citrate, ethylene glycol, silicic acid anhydride and water and the paints on the mica plates were dried at 120C +
6C, resulting in paint layers having constituents shown in Table 3.
Table 3 Constituent of paint Paint No. 1 No. 2 NQ. 3 No. 4 tungsten carbide 18 wt% 26 wt% 33 wt% 42 wt%
zirconium oxide 12 wt% 13 wt% 4 wt% 3 wt%
aluminum nitride 5 wt% 3 wt% 0.6wt% 0.7wt%
molybdenum boride 11 wt% 14 wt% 26 wt% 16 wt%
molybdenum disilicate 21 wt%13 wt% 4 wt% 3 wt%
tungsten 14 wt% 16 wt% 20 wt% 21 wt%
sodium citrate 3 wt% 3 wt% 2 wt% 2 wt%
ethylene glycol 2 wt% 2 wt% 2 wt% 2 wt%
silicic acid anhydride 9 wt%7 wt% 6 wt% 8 wt%
water remnant remnant remnant remnant Maximum temperature Tmax (oC) of the paint layers and current supply time t (sec) were measured in the similar manner to that in the Experimental Example 1. The result of the measurement is shown in Table 4.
Table 4 Paint No. 5 No. 6 No. 7 No. 8 DC12V Tmax (C) 133C 224C 347C 401C
(3A) t (sec) 58 sec. 65 sec. 58 sec. 62 sec.
DC50V Tmax (C) 136C 223C 347C 401C
(3A) t (sec) 32 sec. 36 sec. 41 sec. 42 sec.
DClOOV Tmax (C) 135C 226C 348C 401C
(3A) t (sec) 15 sec. 19 sec. 20 sec. 20 sec.
The temperature increasing rate and the temperature distribution were similar to those in the Experimental Example 1.
Although details are omitted for simplicity of description, it has been found that pyrolytic paint for low and middle temperature range preferably contains metal carbide 15 to 30 wt%, metal oxide 5 to 10 wt%, metal nitride 3 to 5 wt%, metal boride 10 to 15 wt%, metal silicide 10 to 25 wt%, additive metal 10 to 20 wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5 wt% and silicic acid anhydride and/or sodium silicate 5 to 10 wt%. Further, it has been found that pyrolytic paint for high temperature range preferably contains metal carbide 25 to 45 wt%, metal oxide 3 to 5 wt%, metal nitride 0.5 to 1 wt%, metal boride 15 to 30 wt%, metal silicide 0.5 to 10 wt%, additive metal 15 to 25 wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5 wt% and silicic acid anhydride and/or sodium silicate 5 to 10 wt%.
Other metal carbide than those mentioned in the Experimental Examples 1 and 2 may include boron carbide, chromium carbide, etc. Similarly, other metal oxide may include cellium oxide, aluminum oxide, etc., and other metal boride may include titanium boride, etc. Further, it should be noted that the present invention is not limited to the metal mixture of single metal carbide, single metal oxide, single metal nitride and single metal boride. That is, a plural kinds of metal carbide, etc., may be included in the mixture.
[Experimental Example 3]
On the paint layer of any of pyrolytic paints of the Experimental Examples 1 and 2, a reinforcing coating of perhydropolysilazane is formed by painting and the coating was dried at 120C + 6C so that the latter is heat cured at relatively low temperature. It is preferable in order to prevent clacks from occurring after the drying step that the silicon dioxide ceramic coating of perhydropolysilazane is painted on the paint layer to a thickness of in the order of 3~m.
The paint layer strength, the thermal stability, the electric insulation and the chemical resistance of the paint layer having the reinforcing coating were measured and summarized below:
Strength of Paint layer: Pencil Hardness 9H (MV Hardness 600) Thermal Stability : Maximum Durable Temperature Heat Cycle: Durable in -40C
to 400C
Electric Insulation : 101Q /square cm 216633~
Chemical Resistance : 1000 A/min.
(Conc.: hydrofluolic acid 1 +
nitric acid 99) As described, the pyrolytic paint according to the present invention can generate heat enough to make temperature of the paint as high as 400 C or more which is about 4 or more times the maximum temperature achievable by the known pyrolytic paint, with superior temperature rising characteristics. Further, the heat generation in the present pyrolytic paint layer is uniform throughout the surface of the paint layer.
Further, since the silicon dioxide component adheres to a painting surface while forming the lands, it is possible to form a paint layer strongly adhered to a surface of a substrate which may be of ceramics, metal, wood or paper.
Since, therefore, it is possible to reliably paint a flat and smooth surface. Further, since the present pyrolytic paint is water-soluble, inorganic paint, any substrate surface can be painted by any of the printing means such as gravure printing or screen printing, etc., and painting means such as brush painting, spray painting or immersion painting, etc., even if the substrate surface has a three-dimensional configuration.
Further, there is no generation of undesired gas in the drying step after the painting and thus there is no environmental pollution problem.
In the pyrolytic paint according to the present invention, electric power supplied thereto is not lost as optical energy and heat generation from the ceramics component is performed by radiation of far-infrared ray. Thus, substantially the whole electric power supplied can be converted into thermal energy which can be derived very efficiently.
In addition, by forming the reinforcing layer on the paint layer, the mechanical strength, the thermal stability, the electric insulation and the chemical resistance of the paint layer can be improved remarkably.
Claims (7)
1. A water soluble pyrolytic paint characterized by comprising a mixture of at least one metal carbide, at least one metal oxide, at least one metal nitride, at least one metal boride, at least one metal silicide and at least one additive metal and a solvent comprising sodium citrate, ethylene glycol, silicic acid anhydride and/or sodium silicate and water, said mixture and said solvent being mixed and stirred.
2. A water soluble pyrolytic paint claimed in claim 1, characterized by that said water soluble pyrolytic paint, after dried to form a paint layer on a substrate, comprises metal carbide 15 to 45 wt%, metal oxide 3 to 10 wt%, metal nitride 0.5 to 5 wt%, metal boride 10 to 30 wt%, metal silicide 0.5 to 25 wt%, additive metal 10 to 25wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5 wt% and silicic acid anhydride and/or sodium silicate to 10 wt%.
3. A water soluble pyrolytic paint claimed in claim 1, characterized by that said water soluble pyrolytic paint, after dried to form a paint layer on a substrate, comprises metal carbide 15 to 30 wt%, metal oxide 5 to 10 wt% metal nitride 3 to 5 wt%, metal boride 10 to 15 wt%, metal nitride 3 to 5 wt%, metal boride 10 to 15 wt%, metal silicide 10 to 25 wt%, additive metal 10 to 20 wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5% wt% and silicic acid anhydride and/or sodium silicate 5 to 10 wt%.
4. A water soluble pyrolytic paint claimed in claim 1, characterized by that said water soluble pyrolytic paint, after dried to form a paint layer, comprises metal carbide 25 to 45 wt%, metal oxide 3 to 5 wt%, metal nitride 0.5 to 1 wt%, metal boride 15 to 30 wt%, metal silicide 0.5 to 10 wt%, additive metal 15 to 25 wt%, sodium citrate 2 to 3 wt%, ethylene glycol 2 to 2.5 wt% and silicic acid anhydride and/or sodium silicate 5 to 10 wt%.
5. A water soluble pyrolytic paint claimed in claim 1, characterized by that said metal carbide is at least one metal carbide selected from a group consisting of titanium carbide, tungsten carbide, boron carbide, chromium carbide and carbides of equivalent metals, that said metal oxide is at least one metal oxide selected from a group consisting of titanium oxide, zirconium oxide, cellium oxide and oxides of other equivalent metals, that said metal nitride is at least one metal nitride selected from a group consisting of aluminum nitride and nitrides of other equivalent metals, that said metal boride is at least one metal boride selected from a group consisting of chromium boride, molybdenum boride, vanadium boride, titanium boride and borides of other equivalent metals, that said metal silicide is at least one metal silicide selected from a group consisting of molybdenum disilicide and cilicides of other equivalent metals and that said additive metal is at least one metal selected from a group consisting of tungsten, nickel and other equivalent metals.
6. A water soluble pyrolytic paint claimed in any of claims 1 to 5, characterized by that said water soluble pyrolytic paint, after dried to form a paint layer, is painted with a reinforcing paint formed of perhydropolysilazane or the like.
7. A water soluble pyrolytic paint claimed in any of claims 1 to 6, characterized by that said water soluble pyrolytic paint and said reinforcing paint are heat-cured at relatively low temperature, respectively.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002166335A CA2166335A1 (en) | 1995-12-29 | 1995-12-29 | Water soluble pyrolytic paint |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002166335A CA2166335A1 (en) | 1995-12-29 | 1995-12-29 | Water soluble pyrolytic paint |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2166335A1 true CA2166335A1 (en) | 1997-06-30 |
Family
ID=4157259
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002166335A Abandoned CA2166335A1 (en) | 1995-12-29 | 1995-12-29 | Water soluble pyrolytic paint |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2166335A1 (en) |
-
1995
- 1995-12-29 CA CA002166335A patent/CA2166335A1/en not_active Abandoned
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| Date | Code | Title | Description |
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| FZDE | Discontinued |