US3804669A - Flame-resistant resistor coatings - Google Patents
Flame-resistant resistor coatings Download PDFInfo
- Publication number
- US3804669A US3804669A US18678771A US3804669A US 3804669 A US3804669 A US 3804669A US 18678771 A US18678771 A US 18678771A US 3804669 A US3804669 A US 3804669A
- Authority
- US
- United States
- Prior art keywords
- percent
- resistor
- flame
- resistant
- coatings
- 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.)
- Expired - Lifetime
Links
- 238000000576 coating method Methods 0.000 title abstract description 16
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229920001721 polyimide Polymers 0.000 claims abstract description 21
- 229920006389 polyphenyl polymer Polymers 0.000 claims abstract description 21
- 239000008199 coating composition Substances 0.000 claims description 27
- 239000009719 polyimide resin Substances 0.000 claims description 11
- 239000000460 chlorine Substances 0.000 claims description 7
- 239000011521 glass Substances 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 5
- 229910001887 tin oxide Inorganic materials 0.000 claims description 5
- 239000004642 Polyimide Substances 0.000 abstract description 10
- 239000010408 film Substances 0.000 description 24
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 239000011253 protective coating Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- BTAGRXWGMYTPBY-UHFFFAOYSA-N 1,2,3-trichloro-4-(2,3,4-trichlorophenyl)benzene Chemical compound ClC1=C(Cl)C(Cl)=CC=C1C1=CC=C(Cl)C(Cl)=C1Cl BTAGRXWGMYTPBY-UHFFFAOYSA-N 0.000 description 1
- PPBRFJLRPRQPEC-UHFFFAOYSA-N 1,3,4-trichloro-5-(2,3,5-trichlorophenyl)-2-(3,4,5-trichlorophenyl)benzene Chemical compound ClC1=CC(Cl)=C(Cl)C(C=2C(=C(Cl)C(=C(Cl)C=2)C=2C=C(Cl)C(Cl)=C(Cl)C=2)Cl)=C1 PPBRFJLRPRQPEC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- -1 tetracarboxylic acid dianhydride Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
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
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C09D179/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/92—Fire or heat protection feature
- Y10S428/921—Fire or flameproofing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31721—Of polyimide
Definitions
- An object of the present invention is to provide a flame-resistant organic coating composition suitable for the protection of film resistors.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
Flame resistant polyimide resistory coatings containing chlorinated polyphenyl and antimony trioxide.
Description
United States Patent 11 1 Bockstie, Jr. Apr. 16, 1974 FLAME-RESISTANT RESISTOR COATINGS [75] Inventor: Lawrence G. Bockstie, Jr., Bradford, [56] References cued UNITED STATES PATENTS 3,541,036 11/1970 Libackyi 117/161 P [73] Assgnee' Commg Glass 3,247,165 4 1966 Rodia 117 137 3,179,634 4/1965 Edwards 260/78 '11- 2 Filed. o /5 1971 3,034,939 5/1962 Newkirk 106/15 FP 3,108,019 10/1963 Davis 117/201 [21] Appl. No.: 186,787 3,440,215 4/1969 H0166 117/161 P Related Application Data Primary Examiner-Leon D Rosdol [62] Division of Ser. No. 652,412, July 1 l, 1967, Pat. No. Assistant F sposito Attorney, Agent, or Firm-Wa1ter S. Zebrowski [52] US. Cl 117/218, 117/137, 117/161, 1
117/201, 117/232 [57] F [51] Int Cl 344d 1/34 344d Flame reslstant p01y1m1de resistory coatmgs contam- [58] Field of Search 117/232, 201, 161 P, 137; mg chm'maed P1YPheYl and 106/15 FP; 260/28 TF 7 Claims, No Drawings FLAME-RESISTANT RESISTOR COATINGS This is a division of application Ser. No. 652,4l2, filed July ll, 1967.
BACKGROUND OF THE INVENTION The present invention relates to coating compositions for electrical resistors. More specifically, the present invention relates to flame-resistant organic coatings adapted for the protection of electrical film resistors against burning due to severe overload (up to l rated power). 1
THE PRIOR ART Recently, electrical film resistors have come into wide use. Normally, these film resistors comprise a substrate such as glass, coated with a thin film of resistor material such as tin oxide, for example. Also, it is known in the art to overcoat these film resistors with a protective layer. The prior art is faced with the problem, however, that these protective coatings due to the heat resulting from severe overloads on the film resistor, very often burn. This burning of the resistor coating not only results in the destruction of the resistor itself but, very often, results in damage to adjacent elements in the system in which it is employed. The consequent damage to electrical equipment and systems from this burning of resistor coatings has led to an intensive search for a flame-resistant coating, which will not burn due to the heat arising from severe overloads on the resistor.
The film resistors containing the protective coatings of the prior art suffer from the further disadvantage that upon severe overload the protective coatings not only burn, but become electrically conductive. This very often results in external arcing and a failure of the resistor to open the circuit in which it is contained. Accordingly, an intensive search has been conducted for a film resistor protective coating which will not burn under severe overload, and also cause the resistor to open the circuit in which it is contained.
It has been proposed to add several conventional flame-retardants to film resistor protective coatings. These efforts, however, have consistently met with failure. One drawback common to most of the conventional flame-retardant coatings is the fact that they become electrically conductive when the resistor is severely overloaded. This causes the resistor to burn, promotes severe external arcing and does not permit the resistor to open the circuit in which it is contained. Moreover, many of these conventional flame-retardant coatings were ineffective to inhibit burning at the extremely high temperatures (500-600C) attained in film resistors under severe overload.
An object of the present invention is to provide a flame-resistant organic coating composition suitable for the protection of film resistors.
A further object of the present invention is to provide a flame-resistant coating composition suitable for the protection of film resistors which will not burn at the high temperature attained in film resistors upon severe overload.
A further object of the present invention is to provide a flame-resistant coating composition suitable for the protection of film resistors which is resistant to burning and which at the same time promotes the destruction of the resistor during severe overload and thereby opens the circuit.
A further object of the present invention is to provide a flame-resistant coating composition suitable for the protection of film resistors which is a stable mixture, with long pot life and which forms a homogeneous, uniform layer upon coating film resistors.
A further object of the present invention is to provide a flame-resistant coating composition suitable for the protection of film resistors wherein the flame-resistant additive is compatible with the protective coating material and does not alter the chemical or dielectric properties thereof.
BRIEF SUMMARY OF THE INVENTION The objects of the present invention are achieved by the provision of a film resistor protective coating composition comprising a polyimide resin containing from about 1 to 60 percent, preferably from about 2 percent to about 10 percent of a chlorinated polyphenyl and from about 1 percent to about 50 percent, preferably from about 2 percent to about 10 percent of antimony trioxide.
It has recently been discovered that polyimide resins are highly suitable as coating compositions for the protection of film resistors due to their exceptional dielectric properties, their hardness and solvent resistant. Unfortunately, these polyimide resins are suspceptible to burning, at the high temperatures attained in film resistors due to severe overloads much in the same manner as described above. Applicant has found that the addition of from about 1 percent to about 60 percent of chlorinated polyphenyl and from about I to 50 percent of antimony trioxide to a polyimide resin results in a coating composition having vastly improved flameresistant properties. Thus, the coating compositions of the present invention are stable against burning, when resistors containing these coatings are placed under severe overload.
Moreover, the coating compositions of the present invention possess the additional property of being somewhat intumescent. This results in the phenomenon that, frequently, upon the film resistor attaining a high temperature due to severe overload, the coating of the present invention will swell and form a protective cocoon. This cocoon adds further to the protective qualities of the coating of the present invention in that it confines the external arcing. No other coating composition has been found which possesses this intumescent property. It is noteworthy that the polyimide resin coatings alone, i.e., without the addition of chlorinated polyphenyl or antimony trioxide, do not possess intumescent properties. Furthermore, the coating compositions are homogeneous and have long pot lives, unlike the heretofore employed flame-resistant coating compositions.
DETAILED DESCRIPTION OF THE INVENTION The polyimide resins suitable as a base material for the coating compositions of the present invention are described in U.S. Pat. No. 3,179,634. Generally, these cured resins are characterized by a recurring unit having the following structural formula:
wherein R is a tetravalent aromatic radical, preferably containing at least one ring of six carbon atoms, said ring characterized by benzenoid unsaturation, the four carbonyl groups being attached directly to separate carbon atoms in a ring and each pair of carbonyl groups being attached to adjacent carbon atoms in a ring of the R radical; and wherein R is a divalent benzenoid radical containing at least two rings of six carbon atoms, each ring characterized by benzenoid unsaturation, and in which no more than one of the valence bonds is located on any one of said rings of said R radical.
The most preferred of the polyimides is duPonts RK-692, which is a polyimide according to the above structural formula wherein R is and wherein R is Generally, these polyimides are prepared by reacting an appropriate organic diamine with a suitable tetracarboxylic acid dianhydride. This and other processes for the preparation of these polyimides are more specifically described in US. Pat. No. 3,179,634.
Generally, polyimides wherein the degree of polymerization is controlled such that the resin has an inherent viscosity from about 30 to about 90 poises when measured at C. are suitable as base materials for the coating compositions of the present invention.
As mentioned above, the desirable flame-resistant and intumescent properties are imparted to the polyimide resin base material by incorporating therein from about 1 percent to about 60 percent of a chlorinated polyphenyl and from about 1 percent to about 50 percent of antimony trioxide.
The chlorinated polyphenyls are well known in the art, it being preferred that a chlorinated polyphenyl like Aroclor 5460, made by Monsanto, or similar chlorinated polyphenyls having about the same degree of polymerization and degree of chlorination be employed as one of the flame-resistant additives of the present invention.
Suitable chlorinated polyphenyl resins are those sold under the name Aroclor. These materials are prepared by the chlorination of crude biphenyl and are resinous materials possessing high melting points and containing from 18 to 66 percent chlorine. Useful chlorinated polyphenyl resins include Aroclor 1260, Aroclor 1262, Aroclor 1268, Aroclor 1270, Aroclor 4465, Aroclor 5442, Aroclor 2565, and Aroclor 5460, the most preferred being the latter, which has a softening point of about 100 105C.
The incorporation of chlorinated polyphenyl and antimony trioxide into the polyimide base material may be effected by any of the well known, conventional methods.
Film resistors are well known in the art and are generally manufactured as follows. A suitable substrate, such as glass, after being appropriately sensitized according to methods well known in the art is heated to a high temperature and coated with a thin spray ofa solution of stannic chloride. Upon contact of the stannic chloride solution with the hot glass surface, the stannic chloride is pyrolized to tin oxide which deposits out as an extremely thin uniform layer on said glass surface. This tin oxide layer acts as the resistor material. It is to be understood, however, that the coating compositions of the present invention are applicable for the protection of any resistor regardless of its method of preparation, composition, shape or structure.
The coating compositions according to the present invention may be applied to the film resistor by any of the well known coating methods. For example, the composition may be solvent sprayed onto the film resistor, or the film resistors may be dip-coated by immersion thereof in a suitable solution of the coating composition. The coatings may also be applied by brush or roller coating applications. It is to be further understood that the invention is not limited to any particular method of applying the novel coating compositions of the present invention and that any of the conventional, well known coating methods may be employed to effect the deposition of the flame-resistant coating composition on the resistor.
Suitable solvents for use in conjunction with the coating compositions of the present invention are any organic liquids capable of dissolving the components of the composition and which are chemically inert with respect thereto. Suitable solvents include the liquid dialkylcarboxylamides such as N,N-diethylacetamide and dimethyl sulfoxide, and N-methyI-Z-pyrrolidone.
It should also be understood that the coating compositions may be modified with inert pigments, dyes, inorganic and organic fillers as desired. For example, titanium dioxide, carbon, earth pigments or mixtures thereof may be added to the compositions to provide desired colors. Fillers such as asbestos, bentonites, silica, etc. may also be incorporated.
The invention is more specifically explained by the following illustrative examples which are not necessarily intended to be limiting. In these examples, all parts and percentages are by weight except as noted.
EXAMPLE I Parts Polyimide (DuPont RK-692) I00 Chlorinated Polyphenyl (Monsanto Arochlor 5460) I0 Antimony Trioxide 5 EXAMPLE II Parts Polyimide (DuPont RK-692) 100 Chlorinated Polyphenyl (Monsanto Aroclor 5460) 20 Antimony Trioxide l EXAMPLE III Parts Polyimide (DuPont RK-692) I00 Chlorinated Polyphenyl (Monsanto Aroclor 5460) Antimony Trioxide 10 The invention herein disclosed may be variously modified and embodied within the scope of the following claims.
What is claimed is:
l. A coated electrical resistor comprising a resistance layer coated with a stable, intumescent coating composition consisting essentially of a polyimide resin containing from about 1 percent to about 60 percent of a chlorinated polyphenyl and from about 1 percent to about 50 percent antimony trioxide, all percentages being weight percentages of the amount of polyimide resin, which coated electrical resistor upon electrical overload does not burn and which confines external electrical arcing.
2. The resistor of claim 1 wherein said coating composition contains from about 2 percent to about 10 percent of a chlorinated polyphenyl and from about 2 percent to about 10 percent of antimony trioxide.
3. The resistor of claim 1 wherein said polyimide resin is one having the recurring unit:
wherein R is a tetravelent radical containing at least one ring of six carbon atoms, said ring characterized by benzenoid unsaturation, the four carbonyl groups being attached directly to separate carbon atoms in a ring and each pair of carbonyl groups being attached to adjacent carbon atoms in a ring of the R radical; and wherein R is a divalent benzenoid radical containing at least two rings of six carbon atoms, each ring characterized by benzenoid unsaturation, and in which no more than one of the valence bonds is located on any one of said rings of said R radical.
4. The resistor of claim 1 wherein said chlorinated polyphenyl is one containing from 18 to 66 percent chlorine.
5. The resistor of claim 3 wherein said coating composition contains 20 percent chlorinated polyphenyl containing from l8 to 66 percent chlorine and 10 percent antimony trioxide.
6. The resistor of claim 1 comprising a substrate having coated thereon a thin resistance layer of tin oxide.
7. The resistor of claim 6 wherein said substrate is glass.
Claims (6)
- 2. The resistor of claim 1 wherein said coating composition contains from about 2 percent to about 10 percent of a chlorinated polyphenyl and from about 2 percent to about 10 percent of antimony trioxide.
- 3. The resistor of claim 1 wherein said polyimide resin is one having the recurring unit:
- 4. The resistor of claim 1 wherein said chlorinated polyphenyl is one containing from 18 to 66 percent chlorine.
- 5. The resistor of claim 3 wherein said coating composition contains 20 percent chlorinated polyphenyl containing from 18 to 66 percent chlorine and 10 percent antimony trioxide.
- 6. The resistor of claim 1 comprising a substrate having coated thereon a thin resistance layer of tin oxide.
- 7. The resistor of claim 6 wherein said substrate is glass.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18678771 US3804669A (en) | 1967-07-11 | 1971-10-05 | Flame-resistant resistor coatings |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65241267A | 1967-07-11 | 1967-07-11 | |
| US18678771 US3804669A (en) | 1967-07-11 | 1971-10-05 | Flame-resistant resistor coatings |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3804669A true US3804669A (en) | 1974-04-16 |
Family
ID=26882411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US18678771 Expired - Lifetime US3804669A (en) | 1967-07-11 | 1971-10-05 | Flame-resistant resistor coatings |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3804669A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3916073A (en) * | 1974-03-11 | 1975-10-28 | Gen Instrument Corp | Process for passivating semiconductor surfaces and products thereof |
| US3935369A (en) * | 1973-11-02 | 1976-01-27 | Western Electric Company, Inc. | Methods of manufacturing an insulated conductor and product produced thereby |
| US4308197A (en) * | 1980-04-21 | 1981-12-29 | Mcdonnell Douglas Corporation | Fire resistant composites |
| US20050126681A1 (en) * | 2000-05-03 | 2005-06-16 | L&P Property Management Company | Composite carpet cushion and process |
| US20070154716A1 (en) * | 2005-12-30 | 2007-07-05 | Saint-Gobain Performance Plastics Corporation | Composite material |
| US20070154717A1 (en) * | 2005-12-30 | 2007-07-05 | Saint-Gobain Performance Plastics Corporation | Thermally stable composite material |
| US20070152195A1 (en) * | 2005-12-30 | 2007-07-05 | Saint-Gobain Performance Plastics Corporation | Electrostatic dissipative composite material |
| US20080224366A1 (en) * | 2005-12-30 | 2008-09-18 | Saint-Gobain Performance Plastics Corporation | Water resistant composite material |
| US20090093581A1 (en) * | 2007-10-04 | 2009-04-09 | Saint-Gobain Performance Plastics Corporation | Thermally stable composite material formed of polyimide |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034939A (en) * | 1960-01-07 | 1962-05-15 | St Regis Paper Co | Laminating method and composition |
| US3108019A (en) * | 1958-02-14 | 1963-10-22 | Corning Glass Works | Method of stabilizing the electrical resistance of a metal oxide film |
| US3179634A (en) * | 1962-01-26 | 1965-04-20 | Du Pont | Aromatic polyimides and the process for preparing them |
| US3247165A (en) * | 1962-11-15 | 1966-04-19 | Minnesota Mining & Mfg | Polyimides |
| US3440215A (en) * | 1965-03-17 | 1969-04-22 | Gen Electric | Aromatic polyimides |
| US3541036A (en) * | 1967-03-30 | 1970-11-17 | Du Pont | Polyamic acid polymer dispersion |
-
1971
- 1971-10-05 US US18678771 patent/US3804669A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3108019A (en) * | 1958-02-14 | 1963-10-22 | Corning Glass Works | Method of stabilizing the electrical resistance of a metal oxide film |
| US3034939A (en) * | 1960-01-07 | 1962-05-15 | St Regis Paper Co | Laminating method and composition |
| US3179634A (en) * | 1962-01-26 | 1965-04-20 | Du Pont | Aromatic polyimides and the process for preparing them |
| US3247165A (en) * | 1962-11-15 | 1966-04-19 | Minnesota Mining & Mfg | Polyimides |
| US3440215A (en) * | 1965-03-17 | 1969-04-22 | Gen Electric | Aromatic polyimides |
| US3541036A (en) * | 1967-03-30 | 1970-11-17 | Du Pont | Polyamic acid polymer dispersion |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3935369A (en) * | 1973-11-02 | 1976-01-27 | Western Electric Company, Inc. | Methods of manufacturing an insulated conductor and product produced thereby |
| US3916073A (en) * | 1974-03-11 | 1975-10-28 | Gen Instrument Corp | Process for passivating semiconductor surfaces and products thereof |
| US4308197A (en) * | 1980-04-21 | 1981-12-29 | Mcdonnell Douglas Corporation | Fire resistant composites |
| US20050126681A1 (en) * | 2000-05-03 | 2005-06-16 | L&P Property Management Company | Composite carpet cushion and process |
| US20070154716A1 (en) * | 2005-12-30 | 2007-07-05 | Saint-Gobain Performance Plastics Corporation | Composite material |
| US20070154717A1 (en) * | 2005-12-30 | 2007-07-05 | Saint-Gobain Performance Plastics Corporation | Thermally stable composite material |
| US20070152195A1 (en) * | 2005-12-30 | 2007-07-05 | Saint-Gobain Performance Plastics Corporation | Electrostatic dissipative composite material |
| US20080224366A1 (en) * | 2005-12-30 | 2008-09-18 | Saint-Gobain Performance Plastics Corporation | Water resistant composite material |
| US20090093581A1 (en) * | 2007-10-04 | 2009-04-09 | Saint-Gobain Performance Plastics Corporation | Thermally stable composite material formed of polyimide |
| US8309645B2 (en) * | 2007-10-04 | 2012-11-13 | Saint-Gobain Performance Plastics Corporation | Thermally stable composite material formed of polyimide |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3804669A (en) | Flame-resistant resistor coatings | |
| US2686738A (en) | Dispersion of polymeric trifluorochloroethylene, method of preparing said dispersion, and method of coating a base therewith | |
| US4578427A (en) | Coating resin composition | |
| US4238528A (en) | Polyimide coating process and material | |
| US2258222A (en) | Methyl aryl silicones and insulated conductors and other products utilizing the same | |
| US3411122A (en) | Electrical resistance element and method of fabricating | |
| KR102417428B1 (en) | Polyamic acid composition comprising alicyclic monomer and trasparent polyimide film using the same | |
| CN109897180B (en) | Polyamide acid solution, transparent polyimide resin film using same, and transparent substrate | |
| US4161564A (en) | Coating formulation, method, and coated substrate | |
| US3803103A (en) | Polyimides from dimer diamines and electrical insulation | |
| KR880001751A (en) | Polytetrafluoroethylene containing coating composition and use thereof | |
| US3104985A (en) | Conducting polymer compositions | |
| US3741929A (en) | Inorganic flameproofing composition for organic materials | |
| US3669738A (en) | Polyester coated wire | |
| US5688841A (en) | Antistatic aromatic polyimide film | |
| US2522501A (en) | Vinyl diaryl ether polymers | |
| KR101292993B1 (en) | Polyimide resin, and liquid crystal alignment layer and polyimide film using the same | |
| US3655607A (en) | Flame-resistant resistor coatings | |
| US2995688A (en) | Electrical device and dielectric material therefor | |
| JPS58103559A (en) | Flame retardant polyamide | |
| US3377310A (en) | Coating compositions containing crosslinkable polyamides dissovled in phenolic solvents | |
| US3788997A (en) | Resistance material and electrical resistor made therefrom | |
| US2686770A (en) | Dispersion of fluorochlorocarbon polymers | |
| US2624777A (en) | Insulated electrical conductor | |
| US2866764A (en) | Ink for printing electrical circuits, process for printing a polymer surface therewith, and resulting article |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: VISHAY INTERTECHNOLOGY, INC., 63 LINCOLN HIGHWAY, Free format text: ASSIGNMENT OF ASSIGNORS INTEREST. SUBJECT TO LICENSE RECITED;ASSIGNOR:CORNING GLASS WORKS;REEL/FRAME:004821/0304 Effective date: 19871110 Owner name: VISHAY INTERTECHNOLOGY, INC.,PENNSYLVANIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CORNING GLASS WORKS;REEL/FRAME:004821/0304 Effective date: 19871110 |
