EP0221907A4 - PAINT COMPOSITION. - Google Patents
PAINT COMPOSITION.Info
- Publication number
- EP0221907A4 EP0221907A4 EP19860901311 EP86901311A EP0221907A4 EP 0221907 A4 EP0221907 A4 EP 0221907A4 EP 19860901311 EP19860901311 EP 19860901311 EP 86901311 A EP86901311 A EP 86901311A EP 0221907 A4 EP0221907 A4 EP 0221907A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- kgs
- bagasse
- insulating coating
- silica
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
-
- 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
-
- 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
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other 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
- C09D7/65—Additives macromolecular
-
- 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
- C09D7/66—Additives characterised by particle size
- C09D7/69—Particle size larger than 1000 nm
-
- 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
- C09D7/70—Additives characterised by shape, e.g. fibres, flakes or microspheres
-
- 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
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/26—Silicon- containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/02—Cellulose; Modified cellulose
Definitions
- PAINT COMPOSITION relates to coatings and paints and in particular, insulating coatings and paints which provide heat insulation.
- the paint industry has been, for many years trying to develop a thermo-insulating paint which can satisfactorily prevent heat loss or heat gain across painted surfaces.
- liquid will be understood to include amorphous, gelatinous, fluid and pourable substances.
- appearance of an asterisk (*) denotes that the substance mentioned is identified by its Trade Mark or registered Trade Mark.
- a high build coating is considered to be a coating, which when dried would be of a thickness in the range of 100 microns (approx . ) up to 5 mm (approx ) .
- an- insulating coating composition comprising:
- an insulating coating comprising:
- a method of producing an insulating coating including the steps of: (a) collecting bagasse; (b) grinding and/or particulating said bagasse to an average particle size of 0.01 mm to 5 mm; and
- Bagasse is a natural substance and is the term applied to the final crushed fibre remaining after milling of sugar cane. It consists of fibre (cellulose), water and a small quantity of sugar. It is generally used as or made into fuel, feed, and fibre board. Bagasse is the main source of fuel in the production of steam for mill operation. In some countries, bagasse is a raw material used for the manufacture of paper.
- an insulating paint comprising a paint base which produces when dried, a membrane of a substantially high build coating; and up to 60% by weight of a combination of silica and bagasse.
- the silica li ⁇ ed is a granular type having a hollow centre, whilst the bagasse is preferably dried then ground up to a consistency wherein the average size of particles is approximately 0.01 mm to 5 mm. Good results have been obtained with a silica known as Q-CEL 450* silica microspheres, which is combined with bagasse into a high build membrane paint.
- Q-CEL 450* or Q-CEL 500* are hollow organo silicon modified borosilicate microspheres and as a commercial product are sold as an odorless dry white powder.
- the microspheres are readily wetted out by organic fluids but resist wetting by water. They typically have a bulk
- liquid displacement 0.15 to 0.5 gm/cm with a mean particle size (diameter) of 65 to 70 microns ranging between 10 to 200 microns.
- silica can be utilised, such as hollow organo silicon modified borosilicate microspheres of different dimensions, solid glass microspheres, which are manufactured from A-glass, which are commercially available in graded sizes from 5 to 5000 microns; ceramic, polymeric and mineral microsperes. Further, combinations of these different "silicas" can be utilised.
- the natural substance bagasse can be replaced by an artifically manufactured substance whose chemical composition is any one of the following, or a combination of any one of the following:
- Impurities water, raw sugar and dirt
- the hardenable liquid base can be a paint or paint base such as an acrylic membrane paint, a copolymer resin, an alkyd resin and any other suitable coating, or liquid base, which will harden.
- Fig. 1 illustrates a test rig
- Fig. 2 is a graphical representation of the results of tests conducted over a 6 hour period on a dried film of a paint to the present invention
- Fig. 3 is a graphical representation of the results of tests conducted over a 48 hour period on the same film of that whose results are shown in Fig. 2.
- INSULATING PAINT EXAMPLE 1 A sample of insulating paint was produced from a paint base, this paint being of an acrylic membrane type as is commonly known in the industry. To this paint base was added 10% by weight of specially treated bagasse. This special treatment consisted of a ground down or particulate bagasse of approximately 0.01 mm to 0.5 mm. To this was further added 5% by weight of Q-CEL 450* spherical silica.
- TEST APPARATUS - (See Fig. 1) The apparatus consisted of 2 cylindrical chambers 1 and 2 fabricated from galvanised sheet steel of 1 mm thickness. Each chamber 1 and 2 has two concentric cylinders 3 and 4 of height 60 cm. Inner cylinder 3 has a 30 cm diameter and outer cylinder 4 has a 40 cm diameter with space 5 between filled with insulation 6 and end spaces sealed with galvanised sheet. Chambers 1 and 2 have galvanised sheet flanges 7 at each end, being some 60 cm square with 30 cm hole 8 in centre and 3 heat sensitive probes 9 sited 120 apart, round the periphery, spaced 5 cm from one end.
- Chambers 1 and 2 are stacked vertically. Lower chamber 2 is heated as required and upper chamber 1 is at ambient temperature of laboratory area, being open at the top.
- chambers 1 and 2 and their volume is an optimum compromise between 2 conflicting factors: 1. It should be large enough to permit valid testing (a sample of membrane say 600-1000 square cm, is a reasonable size) and avoid the difficulties inherent in arranging a very small heat supply with adequate control; and 2. It should be small enough not to require excessive heat input, with the control and insulation problems inherent in containing large amounts of heat, and particularly, circulating air currents minimized so that the temperature measured on both membrane (15) surfaces is sensibly the temperature over the total area.
- incandescent lamp 12 as the heat source in the bottom of lower chamber 2 and having an electric current supply at 50 hertz, variable ⁇ in steps of 1 volt, which is read on a meter connected across the unit input.
- Voltage variation is by WF8(G.R.) Variac* rated at 10 amps, with 60 volts connected across its 0-280V winding, so providing an effective 'band-spread' of more than 4 times that of the Variac. scale.
- Probes 9 were 5 cm from flange 7 in each chamber 1 and 2 because:
- Sample membrane 15 was clamped between flanged ends 7 of the chambers 1 and 2 and through bolted to prevent air leakage. Heat was supplied to bottom chamber 1 and temperature recorded as the.i * average between 3 probes, which differed slightly due to unavoidable air current. Chamber 2 therefore proved,* close to ideal. Probes in top chamber 1 showed no variation, as- predicted.
- the insulating paint of example 1 is a heat barrier, providing almost 99% insertion loss when tested under conditions simulating actual use on roofs and similar use.
- Fig. 2 the lefthand margin represents degrees celcius whilst the the bottom margin represents hours from the start of the test.
- the upper graph represents the temperature of the membrane whilst the lower graph represents the ambient temperature.
- the heat source remained stable at 40°C, one hour after the start of the test run.
- the 3 probes read to within 1°C of each other.
- Fig. 3 the lefthand margin represents degrees Celcius whilst the bottom margin represents the time of day with ambient temperature being varied according to natural conditions over a 48 hour period.
- the figures at the bottom margin represent the time on a 24 hour clock.
- the upper graph represents the temperature of the membrane whilst the lower graph represents ambient temperature.
- the tested membrane had one smooth and one rough surface. As the membrane tested was not of continuous cross-section, (in fact varying from approx 0.2 mm to approx 0.6 mm in some places), this exaggerated the reading for the heat gain of the membrane.
- THERMALLY INSULATING COMPARATIVE EXAMPLE CONTROL
- the tests conducted oir membrane and membrane on galvanised sheet were compared to a "Batt", which is a type of fibreglass insulation used generally by the building industry to insulate roofs and other building elements.
- the batt tested was a rated R2.5 (see Standards Association of Australia A.S. 2627 Part 1, 1983). When tested under the same conditions as the membrane and membrane on galvanised sheet, the performance of the batt was not significantly different from that of the membranes.
- the galvanised sheet metal was placed in the test apparatus and the obverse side was subjected to a temperature of 40 C.
- the initial temperature measurement on the reverse side was measured at 30.6°C at an ambient temperature of 21.1°C, and was measured one hour after the 40°C temperature had stabilised in the heat source chamber.
- BAGASSE 90 Kgs.
- SILICA Hollow organo silicon modified borosilicate microspheres: 30 Kgs. This amount represents approx 4.2% by weight of the total composition
- Water To Viscosity BAGASSE 42.0 Kgs. This amount represents approx 12.7% by weight of total composition excluding water added for viscosity.
- SILICA Hollow organo silicon modified borosilicate: 14.0 Kgs. This amount represents approx 4.2% be weight of total composition excluding water added for viscosity.
- BAGASSE 36 Kgs. This amount represents approx 8.8% by weight of the total composition.
- SILICA Hollow organo silicon modified borosilicate microspheres: 12 Kgs. This amount represents approx 2.9% by weight of the total composition.
- BAGASSE 15 Kgs. This amount represents 11.8% by weight of the total composition.
- SILICA Hollow organo silicon modified borosilicate microspheres: 6 Kgs. This amount represents 4.7% by weight of the total composition.
- BAGASSE 10 Kgs. This amount represents approx 8.4% by weight of the total composition.
- SILICA Hollow organo silicon modified borosilicate microspheres: 5 Kgs. This amount represents approx 4.2% by weight of the total composition
- Example 7 COPOLYMER HARDENABLE BASE
- BAGASSE 15 Kgs. This amount represents approx 12.2% by weight of the total composition.
- SILICA A Hollow organo silicon modified borosilicate microspheres: 5 Kgs. This amount represents approx 4.1% by weight of the total composition.
- Example 8 COPOLYMER HARDENABLE BASE HARDENABLE BASE:
- BAGASSE 15 Kgs. This amount represents 10.7% by weight of the total composition.
- SILICA Hollow organo silican modified borosilicate microspheres: 5 Kgs.
- Example 9 STYRENE ACRYLIC HARDENABLE BASE, HARDENABLE BASE:
- SILICA Hollow organo silicon modified borosilicate microspheres: 65 Kgs. This amount represents approx 9.0% by weight of the total composition.
- BAGASSE 112 Kgs. This amount represents approx 33.9% by weight of total composition excluding water added for viscosity.
- SILICA Hollow organo silicon modified borosilicate
- Example 11 ALKYD RESIN BASS'
- BAGASSE 153 Kgs. This amount represents approx 34.8% by weight of the total composition.
- SILICA Hollow orgono silican modified borosilicate microspheres: 40 Kgs. This amount represents approx 9.1% by weight of the total composition
- BAGASSE 190 Kgs This amount represents approx 39% by weight of the total composition excluding white spirits added to viscosity.
- SILICA Hollow organo silicon modified borosilicate microspheres: 45 Kgs.
- Example 13 STYRENE ACRYLIC HARDENABLE BASE.
- HARDENABLE BASE STYRENE ACRYLIC HARDENABLE BASE.
- Water To Viscosity BAGASSE 195 Kgs. This amount represents approx 45.4% by weight of total composition excluding water added for viscosity.
- All examples of iasulating paints mentioned above can be varied and modified to suit particular applications, conditions and purposes.
- the formulas and compositions may require pigmentation, thereby possibly changing the %-by weight of bagasse and silica.
- silica hollow organo silicon modified borosilicate microspheres
- Q-CEL* The particular brand of silica (hollow organo silicon modified borosilicate microspheres) utilised is Q-CEL*.
- an asterisk (*) denotes that the substance mentioned is identified by its Trade Mark or registered Trade Mark.
- PRODUCTION OF INSULATING COATING When producing .a paint or coating in accordance with the present invention the hardenable liquid base mixture is manufactured separately. To this mixture particulated bagasse is added, being of an average particle size of 0.01 mm to 5 mm, and most preferably 0.01 mm to 0.5 mm. To produce bagasse of the preferred sizes, the raw material is ground or particulated by any means available.
- the silica is then added. If the silica utilised is hollow organo silicon modified borosilicate microspheres, then it must be the last component added, as the hollow nature of the spheres is such that the sphere can be broken.
- silica can make upto 50% by weight of the total composition.
- bagasse can make upto 50% by weight of the total composition.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Nanotechnology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU9629/85 | 1985-03-08 | ||
AUPG962985 | 1985-03-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0221907A1 EP0221907A1 (en) | 1987-05-20 |
EP0221907A4 true EP0221907A4 (en) | 1987-07-23 |
Family
ID=3770967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19860901311 Withdrawn EP0221907A4 (en) | 1985-03-08 | 1986-02-28 | PAINT COMPOSITION. |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP0221907A4 (xx) |
JP (1) | JPS62502408A (xx) |
KR (1) | KR910000413B1 (xx) |
BR (1) | BR8605817A (xx) |
DK (1) | DK535286A (xx) |
FI (1) | FI864546A (xx) |
GR (1) | GR860573B (xx) |
IL (1) | IL78120A0 (xx) |
IN (1) | IN166824B (xx) |
MY (1) | MY102434A (xx) |
NO (1) | NO864458D0 (xx) |
PT (1) | PT82104B (xx) |
WO (1) | WO1986005195A1 (xx) |
ZA (1) | ZA861474B (xx) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2626679B2 (ja) * | 1987-03-25 | 1997-07-02 | 義之 大串 | 結露防止機能を有する断熱材 |
FR2624531B1 (fr) * | 1987-12-14 | 1989-10-20 | Gomez Daniel | Procede de preparation d'un materiau contenant une charge vegetale, utilisation notamment dans le domaine des papiers et cartons |
AUPQ707900A0 (en) | 2000-04-20 | 2000-05-18 | Hutton, Lawrence | Coating composition |
KR100559959B1 (ko) * | 2003-05-17 | 2006-03-13 | 조광페인트주식회사 | 건축용 수성도료의 제조방법 |
CN106905752A (zh) * | 2016-12-09 | 2017-06-30 | 西华大学 | 同时具有隔热性和高热反射率的空心陶瓷微珠 |
PL423413A1 (pl) * | 2017-11-10 | 2019-05-20 | Kofarb Spolka Z Ograniczona Odpowiedzialnoscia | Sposób produkcji masy termoizolacyjnej na bazie mikrosfer mineralnych |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2947713A (en) * | 1954-10-07 | 1960-08-02 | Cabot Godfrey L Inc | Protective coating compositions comprising pyrogenic silica |
DE1519152A1 (de) * | 1962-09-29 | 1970-03-12 | Gruenzweig & Hartmann | Spritzbarer Belag zur Koerperschalldaempfung von Bauteilen |
US3969128A (en) * | 1973-12-06 | 1976-07-13 | Bhaskar Raj Urs | Pigment additive for protective and decorative coatings |
DE3113136A1 (de) * | 1980-04-14 | 1982-03-18 | Vianova Kunstharz AG, 8402 Werndorf | Fassadenfarbe |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1466597A (fr) * | 1965-12-15 | 1967-01-20 | Matière utilisable comme enduit ou crépi pour le bâtiment et procédé pour la fabrication et l'application de la matière conforme à celle obtenue ou similaire | |
DE2445075C3 (de) * | 1973-09-21 | 1979-04-12 | The Fujikura Cable Works, Ltd., Tokio | Verfahren zum Aufbringen einer Schicht aus kunststoffbeschichteten Teilchen aus anorganischem Material |
JPS5328292A (en) * | 1976-08-30 | 1978-03-16 | Hitachi Cable Ltd | Laying do uble messenger cable in duct line |
JPS53111336A (en) * | 1977-03-11 | 1978-09-28 | Toray Ind Inc | Coating composition |
US4240936A (en) * | 1979-05-03 | 1980-12-23 | Henning William J | Aqueous insulative coating compositions containing kaolin and staple fibers |
SE427012B (sv) * | 1979-08-16 | 1983-02-28 | Nielsen Hilmer R | Impregneringskomposition innehallande ett alkaliextrakt av ett lingocellulosamaterial, forfarande for dess framstellning och anvendning av kompositionen for framstellning av byggelement |
US4277355A (en) * | 1979-09-28 | 1981-07-07 | Alexander Farcnik | Insulative fireproof textured coating |
JPS5958065A (ja) * | 1982-09-29 | 1984-04-03 | Toray Ind Inc | 防曇性被膜 |
ZA85159B (en) * | 1984-02-01 | 1986-09-24 | Ppg Industries Inc | Coating compositions containing polymeric microparticles |
JPH0580474A (ja) * | 1991-09-19 | 1993-04-02 | Fuji Photo Film Co Ltd | 写真要素 |
JPH068466A (ja) * | 1992-06-25 | 1994-01-18 | Canon Inc | インク容器、これを用いた記録ヘッドユニットおよびこれを搭載する記録装置 |
JP3369020B2 (ja) * | 1995-02-17 | 2003-01-20 | 日本電子株式会社 | 超小型走査電子顕微鏡 |
-
1986
- 1986-02-25 IN IN163/DEL/86A patent/IN166824B/en unknown
- 1986-02-27 ZA ZA861474A patent/ZA861474B/xx unknown
- 1986-02-27 PT PT82104A patent/PT82104B/pt unknown
- 1986-02-28 WO PCT/AU1986/000048 patent/WO1986005195A1/en not_active Application Discontinuation
- 1986-02-28 GR GR860573A patent/GR860573B/el unknown
- 1986-02-28 KR KR1019860700775A patent/KR910000413B1/ko not_active IP Right Cessation
- 1986-02-28 EP EP19860901311 patent/EP0221907A4/en not_active Withdrawn
- 1986-02-28 BR BR8605817A patent/BR8605817A/pt unknown
- 1986-02-28 JP JP61501505A patent/JPS62502408A/ja active Pending
- 1986-03-11 IL IL78120A patent/IL78120A0/xx unknown
- 1986-11-07 DK DK535286A patent/DK535286A/da not_active Application Discontinuation
- 1986-11-07 FI FI864546A patent/FI864546A/fi not_active IP Right Cessation
- 1986-11-07 NO NO864458A patent/NO864458D0/no unknown
-
1987
- 1987-04-11 MY MYPI87000473A patent/MY102434A/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2947713A (en) * | 1954-10-07 | 1960-08-02 | Cabot Godfrey L Inc | Protective coating compositions comprising pyrogenic silica |
DE1519152A1 (de) * | 1962-09-29 | 1970-03-12 | Gruenzweig & Hartmann | Spritzbarer Belag zur Koerperschalldaempfung von Bauteilen |
US3969128A (en) * | 1973-12-06 | 1976-07-13 | Bhaskar Raj Urs | Pigment additive for protective and decorative coatings |
DE3113136A1 (de) * | 1980-04-14 | 1982-03-18 | Vianova Kunstharz AG, 8402 Werndorf | Fassadenfarbe |
Non-Patent Citations (3)
Title |
---|
CHEMICAL ABSTRACTS, vol. 79, 1973, pages 62-63, abstract 6414r, Columbus, Ohio, US; & ZA-A-72 02 322 (PLASTI-FIBRE FORMULATIONS INC.) 17-11-1972 * |
CHEMICAL ABSTRACTS, vol. 89, no. 20, November 1978, page 84, abstract 165087j, Columbus, Ohio, US; & JP-A-78 28 292 (MARUMASA KAGAKU K.K.) 14-08-1978 * |
See also references of WO8605195A1 * |
Also Published As
Publication number | Publication date |
---|---|
BR8605817A (pt) | 1987-08-11 |
NO864458L (no) | 1986-11-07 |
IL78120A0 (en) | 1986-07-31 |
JPS62502408A (ja) | 1987-09-17 |
MY102434A (en) | 1992-06-30 |
DK535286A (da) | 1986-11-10 |
DK535286D0 (da) | 1986-11-07 |
FI864546A0 (fi) | 1986-11-07 |
GR860573B (en) | 1986-06-27 |
EP0221907A1 (en) | 1987-05-20 |
NO864458D0 (no) | 1986-11-07 |
KR870700232A (ko) | 1987-05-30 |
IN166824B (xx) | 1990-07-21 |
ZA861474B (en) | 1986-10-29 |
WO1986005195A1 (en) | 1986-09-12 |
KR910000413B1 (ko) | 1991-01-25 |
FI864546A (fi) | 1986-11-07 |
PT82104B (en) | 1987-06-08 |
PT82104A (en) | 1986-03-01 |
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