US2611718A - Glass fibers coated with werner type complex and method of making same - Google Patents
Glass fibers coated with werner type complex and method of making same Download PDFInfo
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- US2611718A US2611718A US734862A US73486247A US2611718A US 2611718 A US2611718 A US 2611718A US 734862 A US734862 A US 734862A US 73486247 A US73486247 A US 73486247A US 2611718 A US2611718 A US 2611718A
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- fibers
- glass fibers
- complex
- werner type
- carbon atoms
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Classifications
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/38—Organo-metal compounds
-
- 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
- Y10S220/00—Receptacles
- Y10S220/14—Plastic
-
- 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
- Y10S220/00—Receptacles
- Y10S220/23—Fiberglass
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/294—Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
- Y10T428/2958—Metal or metal compound in coating
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
Definitions
- This invention relates to reinforced synthetic resins or plastics, to a method of producing the same, and to fibrous products especially adapted as the reinforcing medium. More specifically, it relates to a method and reinforced by fibrous material incorporated in or bonded to the plastic.
- the invention hasas its object a reinforced resin or plastic article of high initial strength which will maintain the greater part of that strengthafter severe subjection to moisture.
- the tenacity of the bond between the fibers and plastic may be improved by employing certain unsaturated organic compounds in forming the complex, and that thebeneficial results may be obtained with acido groups containing only 3 to carbon atoms as well as with groups containing over ten carbon atoms.
- complexes are formed by following either of the procedures described in Example IV'and Example V of the above identified Iler patent, but employing, in place of stearic acid, various unsaturated acids including methacrylic, crotonic, furoic, furfurylacrylic and sorbic acid, and highly unsaturated acids derived'from linseed oil and from oiticia oil, and other unsaturated acids in which the unsaturation is in the alpha to beta position.
- various unsaturated acids including methacrylic, crotonic, furoic, furfurylacrylic and sorbic acid, and highly unsaturated acids derived'from linseed oil and from oiticia oil, and other unsaturated acids in which the unsaturation is in the alpha to beta position.
- a base solution of the complex in isopropyl alcohol was used in each case, the solution containing the complex in amounts equalling 6% of chromium, though other solvents such as ethyl, butyl, or propyl alcohol, and other concentrations, say 1 to might be employed.
- the reinforcing fiber may be in any of a number of fabricated forms.
- the fibers may be collected into short lengths of strands or yarns that are loosely associated together in masses, or in some cases bonded together by resinous binding materials into webs or mats.
- Yarns or strands of glass fibers may be interlaced to product where plastic is certain complexes of 6 Claims. (Cl. 117-72) 2 form interwoven or interknitted fabrics, or masses of separated or haphazardly arranged fibers may be bonded together into mats or webs.
- the fibers are associated together in yarns or strands they are commonly provided with coatings or sizings of a material such as starch, gelatin, polyvinyl alcohol or the like to aid in holding the fibers together in the strand, and also with coatings of oil, waxes, fats or other materials that lubricate the fiber surfaces.
- a material such as starch, gelatin, polyvinyl alcohol or the like to aid in holding the fibers together in the strand, and also with coatings of oil, waxes, fats or other materials that lubricate the fiber surfaces.
- the complex of the present invention may be applied to the fibers of any of the fabricated forms mentioned either by spraying or dipping. Usually a dilute solution of the complex is employed, for example, two parts of the previously mentioned base solution in 98 parts of water, but other concentrations may be employed if desired.
- the fibrous material is then dried either by exposing it to the air for the necessary lengthof time or by heating it to temperatures of from about 200 F. for approximately 15 minutesto about 225 F. for two or three minutes. The'dry ing renders the complexinsoluble in water.
- the binder and lubricant ordinarily present on'the fiber surfaces is removed prior to application of the complex. This removal may be accomplished by washing the fibrous material with water containing detergents or by cleaning the fibrous material with solvents depending upon the particular type of sizing present on the fiber surfaces. In all cases the sizing is easily removed by heating the fibrous material to temperatures in the neighborhood of 400 to 700 F. for several minutes to decompose and burn oil all organic material on the surfaces of the fibers.
- the fibrous material treated as just described is then combined with synthetic resins or plastics in conventional manner.
- Fabrics such as cloth or mats of fibers may be impregnated with resins in liquid state and then superposed in a mold and the resin impregnant cured under heat and pressure.
- Masses of loosely associated fibers or strands may be collected into preforms by usual practice and the preforms in turn impregnated with the resinous material which is then cured under heat and pressure.
- the invention has been found paticularly valu able in connection with resins of the low pressure thermosetting, non-condensing type.
- Resins that may be used with the invention are allyl type resins such as those disclosed in United States Patents Nos. 2,318,959, 2,385,911, and 2,401,549; styrene alkyd resins, for instance those disclosed in Patents Nos. 2,381,969, and 2,397,240; allyl co- 'No;2,37 3,06" 7 polymerized mixture of an unsaturated acid: such as maleic anhydride with an ole- 'finic compound such as dimethallyl ether; and
- dimethacrylates for instance, the resins disclosed in Patents Nos. 2,332,461 and 2,379,246.
- Styrene copolymers, bimethacrylates and styrene-meth-, acrylate copolymers may also be used.
- Low pressure phenolic resins of the conventional kind are also usable with the present invention.
- the invention also displays some benefit where natural rubber and synthetic rubber, such as a butadiene acrylonitrile copolymerization product is vulcanized in place on glass fiber surfaces.
- the preferable manner of applying the complex to the fiber surfaces is by the aftertreatments referred to above, it is also possible to apply the complexes to the fibers immediately after their formation and as they are collected into strands or mats. In these cases it is desirable to combine the complex with a sizing or binding material for the fibers that is in aqueous solution or dispersion, and to apply the resulting mixture as by spraying or wiping it onto the fibers as they are collected into a strand or by spraying or flowing the mixture onto the fibers as they are collected into a mat.
- a size or binder of this type may include about 2 to 15% synthetic resin such as methyl methacrylate, polystyrene, phenol formaldehyde, or other resin such as any of those previously mentioned, and .2 to 5% of the 6% base solution of the chromium complex.
- synthetic resin such as methyl methacrylate, polystyrene, phenol formaldehyde, or other resin such as any of those previously mentioned, and .2 to 5% of the 6% base solution of the chromium complex.
- Example P Per cent Polyvinyl acetate emulsion (50% solids) 5 Methacrylato chromic chloride (6% base solution) 2 Water 93 7
- Example I I a Per cent Polybutyl methacryla-te (50% water dispersion) l5 Furfurylacrylato chromic chloride (6% base solution) 5 Water 80 This composition is wiped onto the fiber surfaces as they are collected into a strand. The resulting strand may then be twisted and plyed with other yarns, the plyed yarns woven into cloth, and the cloth employed as the reinforcing fibrous material in a plastic laminate.
- An article of manufacture comprising glass fibers and a coating insolubilized on the glass fiber surfaces to render the surfaces more receptive to polyester resins, said coating comprising a complex compound of the Werner type in which a trivalent nuclear chromium atom is coordinated with an unsaturated acido group having from 3 to 7 carbon atoms in which the unsaturated group is between the alpha and beta carbon atoms.
- An article of manufacture comprising glass fibers and a coating of a copolymer of maleic anhydride and dimethallyl ether on the glass fiber surfaces and a, complex compound of the Werner type in which a trivalent nuclear chromium atom is coordinated with an alpha, beta unsaturated acido group having from 3 to 7 carbon atoms to improve the adherence of the resinous material to the glass fiber surfaces.
- a method of modifying glass fiber surfaces to make them more receptive to polyester resin comprising treating the glass fiber surfaces with a complex compound of the Werner type in which a trivalent nuclear chromium atom is coordinated with an alpha, beta unsaturated acido group having 3 to 7 carbon atoms and insolubilizing the Werner complex compound on the glass fiber surfaces by drying.
- the method of modifying glass fibers to make their surfaces more receptive to polyester resins comprising treating the glass fibers with a complex compound of the Werner type in which the trivalent nuclear chromium atom is coordinated with an acido group unsaturated between. the alpha and. beta position. and having from 3 to 7 carbon atoms, and baking the treated glass fibers at a temperature of about 225 F. to insolubilize the Werner complex compound on the glass fiber surfaces.
Description
Patented Sept. 23, 1952 -oN IT-E o STATE 2,611,718 FF E TYPE COMPLEX AND 'METHOD 1 OF ,1
MAKING SAME Robert Steinman,
Newark, Ohio, assignor to Owens-Corning Fiberglas Corporation, a corporation of Delaware NoDrawing. ApplicationMarch 14, 1947, Serial No. 734,862
This invention relates to reinforced synthetic resins or plastics, to a method of producing the same, and to fibrous products especially adapted as the reinforcing medium. More specifically, it relates to a method and reinforced by fibrous material incorporated in or bonded to the plastic.
The invention hasas its object a reinforced resin or plastic article of high initial strength which will maintain the greater part of that strengthafter severe subjection to moisture.
In a patent to Ralph K. Iler for Chemical Process and Product, No. 2,273,040, granted February 17, 1942, there is disclosed the manufacture of complex compounds of the Werner type in which a trivalent nuclear chromium atom is coordinated with an acyclic carboxylic acido group having at least ten carbon atoms. These complexes are disclosed as being initially water soluble, but as becoming water insoluble when dried upon fabric, and as imparting marked hydrophobic characteristics'to fabrics on which they are dried.
I have discovered that the Werner type properly applied to the surfaces of reinforcing fibers, such as glass fibers, employed to reinforce plastics greatly aids in maintaining the strength properties of the reinforced plastic in the presence of moisture. 1
More specifically, I have discoveredthat the tenacity of the bond between the fibers and plastic may be improved by employing certain unsaturated organic compounds in forming the complex, and that thebeneficial results may be obtained with acido groups containing only 3 to carbon atoms as well as with groups containing over ten carbon atoms.
In applications of the invention, complexes are formed by following either of the procedures described in Example IV'and Example V of the above identified Iler patent, but employing, in place of stearic acid, various unsaturated acids including methacrylic, crotonic, furoic, furfurylacrylic and sorbic acid, and highly unsaturated acids derived'from linseed oil and from oiticia oil, and other unsaturated acids in which the unsaturation is in the alpha to beta position.
A base solution of the complex in isopropyl alcohol was used in each case, the solution containing the complex in amounts equalling 6% of chromium, though other solvents such as ethyl, butyl, or propyl alcohol, and other concentrations, say 1 to might be employed. I
The reinforcing fiber may be in any of a number of fabricated forms. For instance, the fibers may be collected into short lengths of strands or yarns that are loosely associated together in masses, or in some cases bonded together by resinous binding materials into webs or mats. Yarns or strands of glass fibers may be interlaced to product where plastic is certain complexes of 6 Claims. (Cl. 117-72) 2 form interwoven or interknitted fabrics, or masses of separated or haphazardly arranged fibers may be bonded together into mats or webs.
Where the fibers are associated together in yarns or strands they are commonly provided with coatings or sizings of a material such as starch, gelatin, polyvinyl alcohol or the like to aid in holding the fibers together in the strand, and also with coatings of oil, waxes, fats or other materials that lubricate the fiber surfaces.
The complex of the present invention may be applied to the fibers of any of the fabricated forms mentioned either by spraying or dipping. Usually a dilute solution of the complex is employed, for example, two parts of the previously mentioned base solution in 98 parts of water, but other concentrations may be employed if desired. The fibrous material is then dried either by exposing it to the air for the necessary lengthof time or by heating it to temperatures of from about 200 F. for approximately 15 minutesto about 225 F. for two or three minutes. The'dry ing renders the complexinsoluble in water.
In most instances it has been found that better results are accomplished if the binder and lubricant ordinarily present on'the fiber surfaces is removed prior to application of the complex. This removal may be accomplished by washing the fibrous material with water containing detergents or by cleaning the fibrous material with solvents depending upon the particular type of sizing present on the fiber surfaces. In all cases the sizing is easily removed by heating the fibrous material to temperatures in the neighborhood of 400 to 700 F. for several minutes to decompose and burn oil all organic material on the surfaces of the fibers.
The fibrous material treated as just described is then combined with synthetic resins or plastics in conventional manner. Fabrics such as cloth or mats of fibers may be impregnated with resins in liquid state and then superposed in a mold and the resin impregnant cured under heat and pressure. Masses of loosely associated fibers or strands may be collected into preforms by usual practice and the preforms in turn impregnated with the resinous material which is then cured under heat and pressure.
The invention has been found paticularly valu able in connection with resins of the low pressure thermosetting, non-condensing type. Resins that may be used with the invention are allyl type resins such as those disclosed in United States Patents Nos. 2,318,959, 2,385,911, and 2,401,549; styrene alkyd resins, for instance those disclosed in Patents Nos. 2,381,969, and 2,397,240; allyl co- 'No;2,37 3,06" 7 polymerized mixture of an unsaturated acid: such as maleic anhydride with an ole- 'finic compound such as dimethallyl ether; and
dimethacrylatesfor instance, the resins disclosed in Patents Nos. 2,332,461 and 2,379,246. Styrene copolymers, bimethacrylates and styrene-meth-, acrylate copolymers may also be used. Low pressure phenolic resins of the conventional kind are also usable with the present invention. The invention also displays some benefit where natural rubber and synthetic rubber, such as a butadiene acrylonitrile copolymerization product is vulcanized in place on glass fiber surfaces.
While the preferable manner of applying the complex to the fiber surfaces is by the aftertreatments referred to above, it is also possible to apply the complexes to the fibers immediately after their formation and as they are collected into strands or mats. In these cases it is desirable to combine the complex with a sizing or binding material for the fibers that is in aqueous solution or dispersion, and to apply the resulting mixture as by spraying or wiping it onto the fibers as they are collected into a strand or by spraying or flowing the mixture onto the fibers as they are collected into a mat. A size or binder of this type may include about 2 to 15% synthetic resin such as methyl methacrylate, polystyrene, phenol formaldehyde, or other resin such as any of those previously mentioned, and .2 to 5% of the 6% base solution of the chromium complex. Examples of fiber-treating compositions of this type are as follows:
Example P Per cent Polyvinyl acetate emulsion (50% solids) 5 Methacrylato chromic chloride (6% base solution) 2 Water 93 7 Example I I a Per cent Polybutyl methacryla-te (50% water dispersion) l5 Furfurylacrylato chromic chloride (6% base solution) 5 Water 80 This composition is wiped onto the fiber surfaces as they are collected into a strand. The resulting strand may then be twisted and plyed with other yarns, the plyed yarns woven into cloth, and the cloth employed as the reinforcing fibrous material in a plastic laminate.
The adhesion of the plastic to the fibers, and
the consequent initial strength of the laminate or fiber-reinforced article, was found to be increased by each of the complexes employed; but a far greater advantage was the fact that the treatment mitigated the deterioration in strength due to exposure to moisture, and the longer and more severe the exposure to moisture, the more marked became the superiority of the treated laminates. It is believedthat the conjugated group in. the complex aids in obtaining a good bond. All unsaturated organic acido groups available for test gave positive results, but preference is given to the monovalent aliphatic acido group with uh.- saturated carbon-to-carbon linkage adjacent the alpha carbon atomtherein.
Examples QH2=C(Cl-l3) -COOH, CH2=CHCOOH Reference is made to my copending application Ser; No- 741,939, filed on. April 16, 1947, now Patent 2,552,910 which describes and claims. the
broad concept of treating glass fiber surfaces with a Werner type complex compound having an acido group of 1 to 6 carbon atoms which contains a functional group to improve the adhesion of certain materials for the glass fiber surfaces.
While the ultimate object is a strong and moisture-resistant reinforced plastic, it will be readily understood that the fiber of glass or the like, treated with the chrome complex so as to be ready for use as reinforcement for plastics, is likewise an article of commerce, usable for manufacture with plastics into any desired articles.
Iclaim:
1. An article of manufacture comprising glass fibers and a coating insolubilized on the glass fiber surfaces to render the surfaces more receptive to polyester resins, said coating comprising a complex compound of the Werner type in which a trivalent nuclear chromium atom is coordinated with an unsaturated acido group having from 3 to 7 carbon atoms in which the unsaturated group is between the alpha and beta carbon atoms. 1
2. An article of manufacture comprising glass fibers and a coating of a copolymer of maleic anhydride and dimethallyl ether on the glass fiber surfaces and a, complex compound of the Werner type in which a trivalent nuclear chromium atom is coordinated with an alpha, beta unsaturated acido group having from 3 to 7 carbon atoms to improve the adherence of the resinous material to the glass fiber surfaces.
3. An article of manufacture as claimed in claim 1 inwhich the acido group is a metha crylate.
e. A method of modifying glass fiber surfaces to make them more receptive to polyester resin comprising treating the glass fiber surfaces with a complex compound of the Werner type in which a trivalent nuclear chromium atom is coordinated with an alpha, beta unsaturated acido group having 3 to 7 carbon atoms and insolubilizing the Werner complex compound on the glass fiber surfaces by drying.
5. The method of modifying glass fibers to make their surfaces more receptive to polyester resins comprising treating the glass fibers with a complex compound of the Werner type in which the trivalent nuclear chromium atom is coordinated with an acido group unsaturated between. the alpha and. beta position. and having from 3 to 7 carbon atoms, and baking the treated glass fibers at a temperature of about 225 F. to insolubilize the Werner complex compound on the glass fiber surfaces.
6. The method of modifying glass fiber surfaces to make them more receptive to polyester resins comprising treating the glass fibers with a complex compound of the Werner type in which the trivalent nuclear chromium atom is. coordinated with a methacrylate group.
ROBERT STEINMAN.
REFERENCES CITED The following references are of. record in the file of this patent:
UNITED STATES PATENTS
Claims (1)
1. AN ARTICLE OF MANUFACTURE COMPRISING GLASS FIBERS AND A COATING INSOLUBILIZED ON THE GLASS FIBER SURFACES TO RENDER THE SURFACES MORE RECEPTIVE TO POLYESTER RESINS, SAID COATING COMPRISING A COMPLEX COMPOUND OF THE WERNER TYPE IN WHICH A TRIVALENT NUCLEAR CHROMIUM ATOM IS COORDINATED WITH AN UNSATURATED ACIDO GROUP HAVING FROM 3 TO 7 CARBON ATOMS IN WHICH THE UNSATURATED GROUP IS BETWEEN THE ALPHA AND BETA CARBON ATOMS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US734862A US2611718A (en) | 1947-03-14 | 1947-03-14 | Glass fibers coated with werner type complex and method of making same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US734862A US2611718A (en) | 1947-03-14 | 1947-03-14 | Glass fibers coated with werner type complex and method of making same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2611718A true US2611718A (en) | 1952-09-23 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US734862A Expired - Lifetime US2611718A (en) | 1947-03-14 | 1947-03-14 | Glass fibers coated with werner type complex and method of making same |
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| Country | Link |
|---|---|
| US (1) | US2611718A (en) |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2702241A (en) * | 1950-10-07 | 1955-02-15 | Hawley Products Co | Glass fiber material |
| US2733182A (en) * | 1956-01-31 | Prdcess and product | ||
| US2746896A (en) * | 1951-12-06 | 1956-05-22 | Lof Glass Fibers Co | Reinforced plastic articles |
| US2757104A (en) * | 1953-04-15 | 1956-07-31 | Metalholm Engineering Corp | Process of forming precision resistor |
| US2764085A (en) * | 1952-01-10 | 1956-09-25 | Dick Co Ab | Masters for planographic printing |
| US2775022A (en) * | 1950-10-23 | 1956-12-25 | Archibald H Davis | Siliceous strand |
| US2797163A (en) * | 1952-11-22 | 1957-06-25 | Walter J Smith | Method of making filter media |
| DE1022380B (en) * | 1954-09-17 | 1958-01-09 | Reichhold Chemie Ag | Process for the production of shatterproof laminated glass |
| US2859109A (en) * | 1954-12-31 | 1958-11-04 | Hawley Products Co | Felted products containing glass filaments |
| US2932601A (en) * | 1954-11-12 | 1960-04-12 | Hawley Products Co | Process of preparing felted products containing hydratable and non-hydratable fibers |
| US2971907A (en) * | 1955-08-17 | 1961-02-14 | Walter J Smith | Filter media and method of making |
| US3014835A (en) * | 1957-12-23 | 1961-12-26 | Armstrong Cork Co | Water-laid inorgainic product |
| US3031099A (en) * | 1953-06-19 | 1962-04-24 | White Sewing Machine Corp | Pressure vessel and method of making the same |
| US3047156A (en) * | 1959-05-01 | 1962-07-31 | Smith Corp A O | Reinforced plastic porous tubular structure and method of manufacture |
| US3054695A (en) * | 1957-06-24 | 1962-09-18 | Loeb Leopold | Procedure for producing textiles resistant to chemical warfare liquids |
| US3068125A (en) * | 1957-06-24 | 1962-12-11 | Jr Robert L Clayton | Treatment of textile materials for repellency to chemical warfare liquids |
| US3081195A (en) * | 1959-07-13 | 1963-03-12 | Owens Corning Fiberglass Corp | Glass fibers coated with an organosilicon polyol |
| US3085919A (en) * | 1958-01-31 | 1963-04-16 | Exxon Research Engineering Co | Laminated articles of reinforced plastics and methods of making same |
| US3097963A (en) * | 1959-03-30 | 1963-07-16 | Owens Corning Fiberglass Corp | Sized glass fibers and composition |
| US3282338A (en) * | 1962-06-06 | 1966-11-01 | Continental Oil Co | Method for consolidating material |
| US3310457A (en) * | 1962-11-29 | 1967-03-21 | Du Pont | Glass-reinforced epoxide resin laminate and method of making same |
| US3311528A (en) * | 1962-12-05 | 1967-03-28 | Owens Corning Fiberglass Corp | Neoprene-glass fiber structures and method for preparation |
| US4251577A (en) * | 1979-07-09 | 1981-02-17 | Owens-Corning Fiberglas Corporation | Asphalt-coated glass fibers |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2273040A (en) * | 1940-09-26 | 1942-02-17 | Du Pont | Chemical process and product |
| US2341885A (en) * | 1941-06-10 | 1944-02-15 | Frank J Sowa | Process for coating plastic materials and the product produced |
| US2356161A (en) * | 1941-07-18 | 1944-08-22 | Du Pont | Chemical process and products |
| US2544666A (en) * | 1946-04-27 | 1951-03-13 | Du Pont | Werner-type chromium compounds as laminating and coating compositions |
-
1947
- 1947-03-14 US US734862A patent/US2611718A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2273040A (en) * | 1940-09-26 | 1942-02-17 | Du Pont | Chemical process and product |
| US2341885A (en) * | 1941-06-10 | 1944-02-15 | Frank J Sowa | Process for coating plastic materials and the product produced |
| US2356161A (en) * | 1941-07-18 | 1944-08-22 | Du Pont | Chemical process and products |
| US2544666A (en) * | 1946-04-27 | 1951-03-13 | Du Pont | Werner-type chromium compounds as laminating and coating compositions |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2733182A (en) * | 1956-01-31 | Prdcess and product | ||
| US2702241A (en) * | 1950-10-07 | 1955-02-15 | Hawley Products Co | Glass fiber material |
| US2775022A (en) * | 1950-10-23 | 1956-12-25 | Archibald H Davis | Siliceous strand |
| US2746896A (en) * | 1951-12-06 | 1956-05-22 | Lof Glass Fibers Co | Reinforced plastic articles |
| US2764085A (en) * | 1952-01-10 | 1956-09-25 | Dick Co Ab | Masters for planographic printing |
| US2797163A (en) * | 1952-11-22 | 1957-06-25 | Walter J Smith | Method of making filter media |
| US2757104A (en) * | 1953-04-15 | 1956-07-31 | Metalholm Engineering Corp | Process of forming precision resistor |
| US3031099A (en) * | 1953-06-19 | 1962-04-24 | White Sewing Machine Corp | Pressure vessel and method of making the same |
| DE1022380B (en) * | 1954-09-17 | 1958-01-09 | Reichhold Chemie Ag | Process for the production of shatterproof laminated glass |
| US2932601A (en) * | 1954-11-12 | 1960-04-12 | Hawley Products Co | Process of preparing felted products containing hydratable and non-hydratable fibers |
| US2859109A (en) * | 1954-12-31 | 1958-11-04 | Hawley Products Co | Felted products containing glass filaments |
| US2971907A (en) * | 1955-08-17 | 1961-02-14 | Walter J Smith | Filter media and method of making |
| US3054695A (en) * | 1957-06-24 | 1962-09-18 | Loeb Leopold | Procedure for producing textiles resistant to chemical warfare liquids |
| US3068125A (en) * | 1957-06-24 | 1962-12-11 | Jr Robert L Clayton | Treatment of textile materials for repellency to chemical warfare liquids |
| US3014835A (en) * | 1957-12-23 | 1961-12-26 | Armstrong Cork Co | Water-laid inorgainic product |
| US3085919A (en) * | 1958-01-31 | 1963-04-16 | Exxon Research Engineering Co | Laminated articles of reinforced plastics and methods of making same |
| US3097963A (en) * | 1959-03-30 | 1963-07-16 | Owens Corning Fiberglass Corp | Sized glass fibers and composition |
| US3047156A (en) * | 1959-05-01 | 1962-07-31 | Smith Corp A O | Reinforced plastic porous tubular structure and method of manufacture |
| US3081195A (en) * | 1959-07-13 | 1963-03-12 | Owens Corning Fiberglass Corp | Glass fibers coated with an organosilicon polyol |
| US3282338A (en) * | 1962-06-06 | 1966-11-01 | Continental Oil Co | Method for consolidating material |
| US3310457A (en) * | 1962-11-29 | 1967-03-21 | Du Pont | Glass-reinforced epoxide resin laminate and method of making same |
| US3311528A (en) * | 1962-12-05 | 1967-03-28 | Owens Corning Fiberglass Corp | Neoprene-glass fiber structures and method for preparation |
| US4251577A (en) * | 1979-07-09 | 1981-02-17 | Owens-Corning Fiberglas Corporation | Asphalt-coated glass fibers |
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