US3220845A - Epoxy resin impregnated photo base and method of preparation - Google Patents
Epoxy resin impregnated photo base and method of preparation Download PDFInfo
- Publication number
- US3220845A US3220845A US271863A US27186363A US3220845A US 3220845 A US3220845 A US 3220845A US 271863 A US271863 A US 271863A US 27186363 A US27186363 A US 27186363A US 3220845 A US3220845 A US 3220845A
- Authority
- US
- United States
- Prior art keywords
- paper
- epoxy resin
- glue
- sized
- photographic
- 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
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Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/775—Photosensitive materials characterised by the base or auxiliary layers the base being of paper
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Definitions
- the present invention relates to photographic material and more particularly to the base material supporting a photosensitive coating, and this application is a continuation in' part of our prior application Serial Number 861,764, filed Dec. 24, 1961, now abandoned.
- An object of the present invention is to provide an impregnant for relatively inexpensive base material to render the base material suitable for supporting a photosensitive material.
- Another object is to provide a photographic sheet having a relatively inexpensive porous base.
- a further object is to provide a treatment for paper to reduce hygroscopic properties and prevent physical States Patent changes caused by atmospheric moisture and to render a base paper chemically inert.
- Another object is to bind impurities in the paper or in animal glue sizes therein from migrating into a photosensitive coating on the paper.
- a further object is to provide a paper of improved strength and improved properties with respect to moisture content therein.
- Another object is to provide a treatment for inexpensive paper to render it suitable for photographic emulsions and provide long shelf life for a sensitized photographic paper made therefrom.
- the present invention provides for the treatment of paper made from any suitable material such as 100% rag, sulfate, or sulfite or combinations of rag and sulfate and sulfite papers, which base paper is impregnated and/or sized with animal glues and organic or inorganic glues and sizes which will provide free or reactive hydrogen groups for cross-linking when combined with a suitable resin material.
- a suitable resin material has been found to be epoxy resins in which the oxygen atom is connected to two adjacent carbon atoms whereby such oxygen atoms may react with free hydrogen groups and particularly the free hydrogen in the amino groups in the animal glues and sizes thereby forming a resinous bond and rendering the sizes non-reactive and binding any objectionable constituent materials'or impurities so that a coating of photosensitive material such as a coating of silver halide gelatin emulsion will not be adversely affected by the paper or the various constituent materials in the paper.
- the fibers are beaten together in a heater where the animal glues and/or sizes are added.
- the resulting paper may have many pores or interstices therein and the paper may 'be sutficiently porous to receive further treatment.
- the papers used are transparent or translucent similar to tracing paper so that developed images in photographic emulsions applied to the paper can be duplicated by contact printing.
- a further treatment according to the present invention is the addition of a solution of an epoxy resin such as that made and sold under the trade name of Epon, which is mixed with a suitable solvent.
- an epoxy resin such as that made and sold under the trade name of Epon
- the web of paper is passed through, a bath by complete immersion in a very liquid solution of epoxy resin so that the paper is completely impregnated, the excess resin being removed by any suitable means such as rollers, air bar, scraper, or the like and returned to the bath. Thereafter the resin retained in the paper is cured.
- the solvent for the resin is evaporated from the web of paper by passing the webthrough an oven or the like, the heating in the oven removes the solvent from the epoxy resin and assists in completing the cure of the epoxy resin impregnated paper.
- the resin reacts with the free hydrogen in the animal glue such as reacting with the hydrogen in the amino groups.
- the amino groups in the animal glue serve the function which had previouslybeen served by curing agents such as ethylenediamine, diethylenetriamine or other curing compounds for the epoxy resin.
- curing agents such as ethylenediamine, diethylenetriamine or other curing compounds for the epoxy resin.
- the present invention avoids these curing agents and avoids the toxic effect, the unpleasant odors and the skin irritations caused by these previously used curing agents for epoxy resins.
- the treatment of the paper web according to the present invention renders the paper non-reactive so that a subsequent coating on the epoxy resin impregnated animal glue sized paper will result in a stable product which will maintain its useful life for an extended period of time.
- Another unexpected and unobvious advantage of applying the epoxy resin directly to the paper without a curing agent is that the viscosity of the epoxy resin solution is kept in the desired liquid condition for the desired degree of penetration into the paper and there is no setting of the epoxy resin until the epoxy resin is in place within the interstices of the paper where the setting reaction with the animal glue occurs. Therefore the liquid epoxy resin solution applied to the paper in accordance with the present invention remains in constant uniform liquid condition during the entire application of the epoxy resin to the paper assuring uniform impregnation and treatment of the paper.
- the epoxy resin treating process according to the present invention therefore can be discontinued at any time by merely removing the paper from the solution of epoxy resin.
- the epoxy resin remaining in the immersion bath will not set and will remain liquid for use at a later time since no. setting or curing agent is present in the resin solution.
- the photographic emulsion coating can be applied by a meniscus coating method with a roller to a continuously moving web. of reactedepoxy resin impregnated paper. Since the epoxy resin and the animal glue sizes in the paper web have reacted, there should be no tendency toward further reaction which could adversely affect the photographic emulsion.
- the photographic emulsion may be in the form of a silver halide gelatin emulsion, a dichromate emulsion, an emulsion hardenable by means of diazido compound, or the like.
- Suitable liquid formula! lions having the desired low viscosity for impregnating the web of paper have been found to be:
- Epon 1001 percent 45 Toluene do 30-40 Ethyl acetate do 510 Xylene gram 30 Ethyl acetate gr Epon 1001 gr 30 Toluene gr 35 Xylene gr 35 Epon 834 gr 25 Epon 828 gr l5 Epon is a trade name of an epoxy resin composition and is described in Technical Publication SC-52-3l of the Shell Chemical Corporation published in 1952. The chemical structure of the Epon resin is indicated on page 7 of this publication to be as follows:
- Epon 1001,834, and 828 have the same chemical structural formula with only the n varying and have properties as indicated in the table on page 6 of the same publication.
- Epon 1001 has a melting point between 64 and 76 degrees centigrade and an epoxide equivalent of 450-525.
- Epon 834 is a liquid having a melting point between 20 and 28' degrees centigrade and an epoxide equivalent of 225-590.
- Epon-828 is a liquid with a melting point between 8 Ind 12 degrees Centigrade and an epoxide equivalent of 190-210.
- the paper with or without the photosensitive coating thereon may have images. drawn thereon so that photocopies may be altered and both positive and negative photocopies can be made.
- a non-reactive paper for use as a photographic base comprising a 100% cotton fiber paper sized with an animal glue leaving approximately 3% of the glue in the paper based on weight of the sized paper, epoxy resin of the general structure:
- n may vary within a range where the melting 4.
- the method providing non-reactive paper base for glue rendering the sized paper substantially non-reac- 5 photographic sheets to be subsequently coated with a tive with photographic sensitive coatings applied to the photosensitive coating comprising, treating a base paper paper. sheet which has been sized with animal glue in the manu- 2.
- a sheet material suitable for receiving photosensifacture thereof with an epoxy resin, of the general structive coatings comprising a good quality fibrous material ture:
- n may vary within a range where the melting sized with animal glue and reacted with epoxy resin of point is generally between 8 and 76 degrees centigrade the general structure: I and the epoxide equivalent is generally between 190 and 590 and without further catalyst, said resin being of thin wherein n may vary within a range where the melting consistency in an aqueous solution penetrating the pores point is generally between 8 and 76 degrees centigrade of the paper base and intermingling with the animal glue and the epoxide equivalent is generally between 190 and in intimate association whereby the epoxy resin is cured 590 and without further catalyst, said resin impregnated by the reaction with the animal glue in situ within the within the sheet material subsequent to the animal glue pores of the paper thereby coating impurities and presizing of the sheet material to cause the animal glue and venting further activity of the animal glue and impurities epoxy resin to combine forming a product which renders with a photosensitive coating to be subsequently applied.
- the animal glue and the sheet material substantially non- 6.
- a paper sheet for receiving a photographic coating on at least one surface thereof without adverse effect on v References Cited by h Examiner the photographic coating comprising a paper sheet having UNITED STATES PATENTS an animal glue sizing impregnated within said at least 0 2,330,116 3/1959 p et aL one surface thereof, and in which the said at least one 2 3 2 250 4 1959 Baker 260 6 surface has been thereafter treated with a very liquid and Y 2,913,356 11/1959 S h d 162 1 4 penetrating solution of an epoxy resin free of a curing 3,041,195 6/ 1962 Saewert et al. agent, said resin being of the general structure: 40 3,012,487 12/1963 Mika. /O ⁇ OH: OH CH: O CHgCHz-CH:[O 30CHr-H-CHzhOQ-OOCHs-Cfilfjfl,
- 21 may vary within a range where the melting FOREIGN PATENTSv point is generally between 8 and 76 degrees centigrade 586 856 11/1959 Canada and the epoxide equivalent is generally between 190 and 4/1959 Great B'ritain 590 and without further catalyst, and which solution of epoxy resin free of a curing agent penetrates said at least OTHER REFERENCES one surface of the paper sheet into effective intermingling Lee et a] p y Resins McGraw Hill Y 1957 combination with the amnie groups present in the animal page glue rendering the animal glue non-reactive, the cured Nebleuef Photography 5th 1952 -161 epoxy resin effectively coating objectionable impurities Neblette" F 6th edmon 1962 page in said paper sheet adjacent said at least one surface thereof so that said at least one surface of the paper sheet may receive a photographic coating.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
Description
Claims (2)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US271863A US3220845A (en) | 1963-04-10 | 1963-04-10 | Epoxy resin impregnated photo base and method of preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US271863A US3220845A (en) | 1963-04-10 | 1963-04-10 | Epoxy resin impregnated photo base and method of preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
US3220845A true US3220845A (en) | 1965-11-30 |
Family
ID=23037409
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US271863A Expired - Lifetime US3220845A (en) | 1963-04-10 | 1963-04-10 | Epoxy resin impregnated photo base and method of preparation |
Country Status (1)
Country | Link |
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US (1) | US3220845A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3478716A (en) * | 1963-03-07 | 1969-11-18 | Kimberly Clark Co | Printable paper product having a cellular coating containing pigment and a reaction product of protein and an epoxy resin defining the cell walls |
US20100008989A1 (en) * | 2008-06-12 | 2010-01-14 | Ishay Attar | Process for manufacture of gelatin solutions and products thereof |
US20100063459A1 (en) * | 2006-12-15 | 2010-03-11 | Orahn Preiss-Bloom | Gelatin-transglutaminase hemostatic dressings and sealants |
US20110086014A1 (en) * | 2008-06-18 | 2011-04-14 | Ishay Attar | Method for enzymatic cross-linking of a protein |
US8703117B2 (en) | 2008-06-18 | 2014-04-22 | Lifebond Ltd. | Cross-linked compositions |
US8961544B2 (en) | 2010-08-05 | 2015-02-24 | Lifebond Ltd. | Dry composition wound dressings and adhesives comprising gelatin and transglutaminase in a cross-linked matrix |
US9066991B2 (en) | 2009-12-22 | 2015-06-30 | Lifebond Ltd. | Modification of enzymatic crosslinkers for controlling properties of crosslinked matrices |
US11998654B2 (en) | 2018-07-12 | 2024-06-04 | Bard Shannon Limited | Securing implants and medical devices |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2880116A (en) * | 1955-11-01 | 1959-03-31 | Rohm & Haas | Coated materials and methods for producing them |
GB811153A (en) * | 1956-03-13 | 1959-04-02 | Ici Ltd | Improved photographic process |
US2882250A (en) * | 1955-07-07 | 1959-04-14 | Stauffer Chemical Co | Process for preparing epoxy resin modified proteins and compositions resulting therefrom |
CA586856A (en) * | 1959-11-10 | Glaser David | Curing epoxy resins with polyamine and polyamide | |
US2913356A (en) * | 1955-06-28 | 1959-11-17 | Shell Dev | Preparation of paper having improved wet strength |
US3012487A (en) * | 1959-04-10 | 1961-12-12 | Shell Oil Co | Polyepoxide compositions |
US3041195A (en) * | 1959-02-26 | 1962-06-26 | Swift & Co | Wrinkle-finish compositions and method of producing same |
-
1963
- 1963-04-10 US US271863A patent/US3220845A/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA586856A (en) * | 1959-11-10 | Glaser David | Curing epoxy resins with polyamine and polyamide | |
US2913356A (en) * | 1955-06-28 | 1959-11-17 | Shell Dev | Preparation of paper having improved wet strength |
US2882250A (en) * | 1955-07-07 | 1959-04-14 | Stauffer Chemical Co | Process for preparing epoxy resin modified proteins and compositions resulting therefrom |
US2880116A (en) * | 1955-11-01 | 1959-03-31 | Rohm & Haas | Coated materials and methods for producing them |
GB811153A (en) * | 1956-03-13 | 1959-04-02 | Ici Ltd | Improved photographic process |
US3041195A (en) * | 1959-02-26 | 1962-06-26 | Swift & Co | Wrinkle-finish compositions and method of producing same |
US3012487A (en) * | 1959-04-10 | 1961-12-12 | Shell Oil Co | Polyepoxide compositions |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3478716A (en) * | 1963-03-07 | 1969-11-18 | Kimberly Clark Co | Printable paper product having a cellular coating containing pigment and a reaction product of protein and an epoxy resin defining the cell walls |
US9636433B2 (en) | 2006-12-15 | 2017-05-02 | Lifebond Ltd | Gelatin-transglutaminase hemostatic dressings and sealants |
US20100063459A1 (en) * | 2006-12-15 | 2010-03-11 | Orahn Preiss-Bloom | Gelatin-transglutaminase hemostatic dressings and sealants |
US8722039B2 (en) | 2006-12-15 | 2014-05-13 | Lifebond Ltd. | Gelatin-transglutaminase hemostatic dressings and sealants |
US9655988B2 (en) | 2006-12-15 | 2017-05-23 | Lifebond Ltd | Gelatin-transglutaminase hemostatic dressings and sealants |
US9017664B2 (en) | 2006-12-15 | 2015-04-28 | Lifebond Ltd. | Gelatin-transglutaminase hemostatic dressings and sealants |
US20100008989A1 (en) * | 2008-06-12 | 2010-01-14 | Ishay Attar | Process for manufacture of gelatin solutions and products thereof |
US20110086014A1 (en) * | 2008-06-18 | 2011-04-14 | Ishay Attar | Method for enzymatic cross-linking of a protein |
US8703117B2 (en) | 2008-06-18 | 2014-04-22 | Lifebond Ltd. | Cross-linked compositions |
US9044456B2 (en) | 2008-06-18 | 2015-06-02 | Lifebond Ltd. | Cross-linked compositions |
US9066991B2 (en) | 2009-12-22 | 2015-06-30 | Lifebond Ltd. | Modification of enzymatic crosslinkers for controlling properties of crosslinked matrices |
US10202585B2 (en) | 2009-12-22 | 2019-02-12 | Lifebond Ltd | Modification of enzymatic crosslinkers for controlling properties of crosslinked matrices |
US8961544B2 (en) | 2010-08-05 | 2015-02-24 | Lifebond Ltd. | Dry composition wound dressings and adhesives comprising gelatin and transglutaminase in a cross-linked matrix |
US11998654B2 (en) | 2018-07-12 | 2024-06-04 | Bard Shannon Limited | Securing implants and medical devices |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SECURITY NATIONAL BANK, A NATIONAL BANKING ASSOCIA Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CHASE MANHATTAN BANK, N.A. THE; A NATIONAL BANKING Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CHEMICAL BANK, A BANKING INSTITUTION OF NY. Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CONTINENTAL ILLINOIS NATIONAL BANK & TRUST CO., OF Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: BANK OF CALIFORNIA N.A. THE; A NATIONAL BANKING AS Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CHEMICAL BANK, A BANKING INSTITUTION OF, NEW YORK Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 |