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Publication numberUS3276933 A
Publication typeGrant
Publication dateOct 4, 1966
Filing dateSep 17, 1962
Priority dateSep 17, 1962
Publication numberUS 3276933 A, US 3276933A, US-A-3276933, US3276933 A, US3276933A
InventorsElmer J Brant
Original AssigneeRadiant Color Company
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Transfer sheet and method
US 3276933 A
Abstract  available in
Images(1)
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Claims  available in
Description  (OCR text may contain errors)

Oct. 4, 1966 E. J. BRANT 3,276,933

TRANSFER SHEET AND METHOD Filed Sept. 17, 1962 INVENTOR ELMER J. BRANT BY WM W ATTORNEYS United States Patent 3,276,933 TRANSFER SHEET AND METHOD Elmer J. Brant, Piedmont, Calif., assignor to Radiant Color Company, Oakland, Calif., a firm composed of Elmer J. Brant and Harry P. Locklin Filed Sept. 17, 1962, Ser. No. 224,891 11 Claims. (Cl. 156-230) This invention relates to transfers. More particularly it relates to dry strip transfers and to the separation 'of the transfer film directly from its backing or base.

In the preferred embodiment, the gist of the present invention lies in coating the transfer sheet "or film (which may have a visible image thereon) directly on the backing or base. This direct application is made possible by incorporating certain fatty acid esters of polyols into the composition of the transfer film. It has been discovered that the transfer'filrn may thereafter be integrally released'and removed from the backing sheet at the appropriate time. Further, the ease of release and removal of the transfer film' from the backing sheet is directly related to the amount of ester incorporated into the transfer film.

The present invention accordingly provides several advantages 'and improvements over prior art techniques. The previously used polyethylene coating on the backing sheet upon which the transfer film has been disposed is eliminated with attendant economic benefits and manufacturing simplification. More important, the present techniques is more positive and reliable in its operation. For example, where the previously used a polyethylene film at times exhibited a tendency to release at inopportune times, the present transfer film uniformly adheres to the backing sheet until used. Further, the transfer film may be made to adhere to the backing sheet as tenaciously as desired by simply adjusting the amount of the ester (to be particularly described hereinafter) to a lesser proportion in the transfer film. When release and separation is desired, the transfer film is still readily removed in one piece. Even at relatively high concentrations where release occurs quite readily, it will not occur before the application of some separation forces.

Thus one of the more outstanding features of the present discovery is the ability to control the degree of retention of the transfer film on the backing sheet by the amount of ester incorporated in the transfer film. As a result of this feature, it has become possible to manufacture feasible transfers of various sizes and shapes and designed for use under various conditions that have heretofore not been possible. In effect, the transfer, at least with respect to the strength of the bond between the transfer film and the backing sheet, can now be custom designed to meet the needs of the particular end use of the transfer.

In the accompanying drawings there is shown in:

FIG. 1, a schematic vertical section through a conventional transfer. 7

FIG. 2 shows a corresponding. schematic vertical section of a transfer made in accordance with the present invention.

I Dry strip transfers as conventionally available today and as illustrated in FIG. 1 consist of a thick paper backing 10 permanently coated with polyethylene or a polyethylene composition 11 on one surface thereof. Transfers are printed upon the polyethylene coated surface of the paper and may comprise a suitable clear resinous layer 12 with an image printed with a plurality of color layers 13, 14 thereon. Commonly, a suitable adhesive 15 is overprinted on the clear and colored layers 12, 13, 14. An adhesive release paper 16 is placed in contact and over adhesive layer 15 to protect the adhesive layer 15 "ice and prevent adherence to anything prior to use of the transfer.

The transfer is applied to any selected object or surface by removing the adhesive release paper 16 and pressing the transfer into contact with the surface, the adhesive layer 15 being disposed in contact with the surface. After a bond between the surface and adhesive layer 15 has been created, the backing sheet 10 together with the polyethylene layer 11 are simultaneously peeled away from the remainder ofthe transfer.

As noted above and in accordance with the present invention, the polyethylene coating 11 has been eliminated. In the preferred embodiment of the present invention, a backing sheet of glassine paper 17 is provided upon which a clear resinous film 18 is directly coated. As before, colored layers 19, 20 defining an image may be printed upon clear layer 18. An adhesive layer 21 is coated on the colored and clear layers and as before, an adhesive release paper 22 is provided. The present transfer is used by removing the adhesive release paper 22, applying the adhesive layer 21 to a selected object or surface, and causing it to bond thereto by means of pressure, for example, where adhesive layer 21 is a pressure sensitive adhesive. The image is then exposed to view through the clear layer 18 by removing glassine paper 17 by pulling and stripping it from clear layer 18.

The direct application of the clear layer 18 to backing sheet 17 with its subsequent capability of being integrally released therefrom is made possible by the incorporation in the clear layer 18 of a fatty acid ester of an alkyl polyol where the ester has at least two free hydroxyl groups in the molecule, i.e., the hydroxyl groups are not esterified during the formation of the ester and are not otherwise in a chemical combination.

For present purposes, suitable esters include all fatty acid esters of monomeric and polymeric alkyl polyols (which may also have various noninterfering substituents thereon) provided at least the minimum number of free hydroxyl groups is present. Preferably, the alkyl polyol is glycerol and the fatty acid portion of the ester is derived from a member of the group consisting of saturated and unsaturated fatty acids having up to about 30 carbon atoms. Accordingly, examples of suitable esters for incorporation in the clear resin layer include, but are not limited, to the following materials:

Glyceryl mono-oleate Glyceryl r'nono-stearate Glyceryl mono-laurate Glyceryl mono-ricinoleate Glyceryl tri-ricinoleate Polyethylene glycol fatty acid ester (Nopco Chemical Co., Catalog Item 1225-L) Whereas all of the above materials illustrate the principle of the invention wherein the requisite number of free hydroxyl groups are present in the molecule by attachment to carbon atoms having only hydrogen otherwise bonded to the hydroxyl containing carbon atom, it is to be noted that the hydroxyl groups may also be associated with non-carbon atoms or with carbon atoms having other than hydrogen atoms bonded thereto. Thus very suitable materials have been found to include esters wherein the hydroxyl groups are part of a sulfonic radical such as in sulfonated castor oil. It should also be noted that the requisite free hydroxyl groups may be contributed by the polyol and/ or by substituents in the fatty acid chain as in n'cinoleate esters.

The selected ester is incorporated into the clear resin, preferably during the formulation of the clear resin and prior to the coating of the clear'resin on the backing sheet, in an amount suflicient to permit integral release of the transfer film from the backing sheet. The precise amount will vary depending upon the clear resin employed, the surface characteristics of the backing sheet, and the type of release desired. In most cases it has been found that about .'3-20% by weight of ester to the clear resinformula (including solvents) provides the desired release characteristics to the transfer. Preferably the ester is added to the clear resin formula in an amountof about .3-5% by weight.

The clear resin is formed from materials Well known in the art and previously used for the formation of the transfer film so long as they are releasable from the backing sheet when used as noted herein. Most of the common film-forming resins have been found to be suitable for present purposes and include the following: vinyl resins,

cellulosic film forming resins such as nitrocellulose, cellulose acetate, and ethyl cellulose, and acrylic resins.

' Some of the polyester resins and particularly the alkyds are not adapted to the formation of the, clear resin-because of their poor or absence of release properties when in combination with the present esters. However, even these materials when used in combination with other suitable resins produce releasable clear resin films.

When desired the color layers printed on the clear film to form the composite transfer film may be made by any of the usual painting or printing processes using any of the various lacquers, paint, and resins normally employed for such purposes in the trade. A preferred technique for application of these layers is by the silk screen procedure.

The backing sheet may be any suitable surface for holding and releasing the transfer film. Preferred materials include vegetable parchment paper and glassine paper. It is desirable to calendar the backing sheetto obtain as high a gloss as possible.

Where an adhesive layer on the color and/or clear resins is desired, thechoice is again wide and in accordance with prior techniques. In the preferred embodiment a pressure sensitive adhesive is employed with a suitable protective adhesive release paper. it should be obvious that where an adhesive is applied to the resin layers it should be of the type permitting mechanical removal of the protective adhesive release paper from the adhesive layer without causing separation of the transfer film from the backing sheet. Mechanical disruption of the bond between the transfer film and the backing sheet occurs only when the adhesive layer has been bonded to a selected surface upon which the transfer film is tov ultimately rest. In the event that removal of the adhesive release paper disturbs the bond between the transfer film and the backing sheet, it would of course only be necessary to reduce the amount of fatty acid ester present in the transfer film.

The following example will illustrate the use of the present invention:

EXAMPLE 2 grams (4%) of glycerol mono-oleate was added to 50 grams of a clear resin film forming solution of ethyl cellulose. The mixture was stirred vigorously with a stirring rod until homogeneous. A thin coating of the mixture was then applied to a piece. of glassine paper (2-40 lbs. laminate, basis 24 x 36) by spreading and rubbing out with a finger tip. It was then allowed to dry. A piece of cellophane adhesive tape was then pressed into bonding contact with the dried coating and pulled away from the glassine paper. The clear resin-ester layer was integrally released and pulled away from the glassine paper.

Where colored resin layers are printed on the dried resin layer to form an image and then over coated with a suitable adhesive, the adhesive surface is pressed into contact with a suitable surface and the glassine paper is then stripped and removed to leave an integral resin layer on the selected surface. The material known as #9010 Pressure Sensitive Adhesive (Cudner & OConnor, Chicago, lllinois) has been used as a pressure sensitive adhesive for this purpose with'excellent results.

Plasticized ethyl cellulose lacquer Component: Amount in grams "Ethyl cellulose 75.0 Dow 276 V2, plasticizer 30.0 Xylene 150.0 Methyl isoamyl ketone 45.0

Plasticized nitrocellulose lacquer Component: Amount in grams Nitrocellulose 45.0 Duraplex ND78, plasticizing alkyd 90.0 Hercoflex 600, plasticizer 13.0 Methyl isoamyl ketone solvent 75.0 Xylene 60.0 Pent-oxone solvent (Shell) 30.0

Cellulose acetate butyrate lacquer Amount in grams Component:

Cellulose acetate butyrate 46.0

40% solution acryloid B82 in toluene 90.0

Plasticizer, Santicizer M17 (Monsanto plasticizer) 9.0

Xylene 55.0

Methyl isoamyl ketone 55.0

Pent-oxone solvent (Shell) 55.0

The various esters enumerated as examples hereinbefore have been incorporated at varying percentages in the above clear resins with successful releaseproperties being exhibited when the combined resin-ester was applied to glassine paper in the manner described above,

Various modifications to the composite transfer of the present invention will be suggested to those skilled in the art, a few of which are here mentioned.- The clearlayer, may be pigmented or dyed where an overall hue is desired for a background. If the clear layer is pigmented or dyed, the color layers can be omitted .and the pigmented clear layer cut' to any desired pattern or image. Another alternative (especially for interior uses where protection is not as vital) is to eliminate the clear layer and employ only resinous color layers. In this case the color layers cooperate directly with the backing sheet in the same way as the clear layer does and of course would have .a suitable ester incorporated therein for obtaining the release properties. Also, it should be noticed that the transfers of the present invention may 'be made for use so that any visual display which may be disposed on the clear layer can be viewed from either side of the transfer as desired by placing the display either' face up, or face down on the clear layer. Placing the display face uppermits for example, the attachment of a transfer to theinside of a window so that the display may be viewed through the window fromthe outside. A further modification would be to place two displays on the clear layer both face 'up and face down in back to back relation so that 'when the transfer is placed on a window it may be viewed from either side of the window. In this latter case an opaque layer between the back to back displays is necessary.

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is understood that certain q al ges andmodifications may be practiced .Wlthin the spirit of the invention as limited only by the scope of the appended claims.

What is claimed is:

1. A transfer comprising: a paper backing sheet selected from the group consisting of glassine and vegetable parchment; a film of resin disposed directly on said paper backing sheet of the type that is releasable from the paper sheet by inclusion of an ester as specified hereinafter in the resin film; and about .320% by weight of the formula (including solvents) of the transfer film resin of an ester operable to cause integral release of the transfer film from the paper at a preselected time only, said ester being a fatty acid ester of an alkyl polyol and having at least two free hydroxyl groups.

2. A transfer in accordance with claim 1 wherein said ester is about .3-5% by weight of the formula (including solvents) of said transfer film and wherein said backing sheet is glassine paper.

3. A transfer film in accordance with claim 1 wherein said ester is a mono-ester of glycerol and the fatty acid portion of the ester is derived from a number of the group consisting of saturated and unsaturated fatty acids having up to about 30 carbon aoms.

4. A transfer in accordance with claim 1 wherein said ester is glyceryl mono-oleate.

5. A transfer in accordance with claim 1 wherein said ester is glyceryl mono-ricinoleate.

6. A transfer in accordance with claim 1 wherein said ester is glyceryl tri-ricinoleate.

7. A transfer in accordance with claim 1 wherein said ester is glyceryl mono-laur-ate.

8. A transfer in accordance with claim 1 wherein said ester is sulfonated castor oil.

9. A transfer comprising a glassine paper backing sheet, a releasable clear resinous transfer film directly coated on said backing sheet, said transfer film formula (including solvents) having incorporated therein about .3-5% by weight of a fatty acid ester of an alkyl polyol, said ester having at least two free hydroxyl groups, a color image printed on the exposed side of said transfer film, an adhesive on the exposed side of said color image and remainder of the exposed side of said transfer film for the bonding thereof to a selected surface, and an adhesive release paper on the said adhesive for protecting said adhesive prior to bonding, said adhesive release paper being mechanically removable from said adhesive Without separating said transfer film from said glassine backing sheet, said fatty acid ester permitting the mechanical separation of said glassine paper backing sheet from said transfer after said adhesive has bonded said color image and transfer film to a selected surface, the resistance to separation of said glassine paper backing sheet from said clear resin film being directly related to the amount of said fatty acid ester incorporated in said transfer film, the resistance increasing with decreasing ester concentration.

10. A method of transferring a releasable resinous film having an image thereon from a glassine paper backing sheet to a selected surface which comprises incorporating into said resinous film formula (including solvents) about .3-20% of a fatty acid ester of an alkyl polyol operable to cause integral release of said resinous film from the glassine paper backing sheet at a preselected time only wherein the ester contains at least two free hydroxyl groups whereby a mechanically disruptable bond is formed between said backing sheet and said resinous film directly related to the amount of the ester incorporated therein, ease of disruption increasing with increasing ester concentration, coating said resinous film with an adhesive, placing said resinous film with its adhesive coating in contact with a selected surface to bond said film to said surface, and stripping the backing sheet from the film to expose the film.

11. A method in accordance with claim 10 wherein said ester is a fatty acid ester of glycerol wherein the acid derived chain has up to about 30 carbon atoms.

References Cited by the Examiner UNITED STATES PATENTS 2,308,900 1/ 1943 Tryon et al. 161406 2,596,179 5/1952 Seymour 161406 2,774,745 12/ 1956 Hedlund 260-13 X 2,811,475 10/ 1957 Edge 161406 3,013,917 12/1961 Karlan et al 161235 3,065,120 11/1962 Avelar 161- 406 3,131,106 4/1964 Mackenzie 161-406 3,170,809 2/ 1965 Barbour 11736.4

EARL M. B ERGERT, Primary Examiner.

R. I. SMITH, M. L. KATZ, Assistant Examiners.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2308900 *Mar 23, 1939Jan 19, 1943Transograph CorpShading film
US2596179 *Jan 4, 1951May 13, 1952B B Chem CoSupported adhesive sheet material unit and method of making the same
US2774745 *Nov 17, 1952Dec 18, 1956Dow CorningHigh-slip nitrocellulose lacquers
US2811475 *Oct 26, 1953Oct 29, 1957Brittains LtdTransfer paper and dry-strip transfers made with such paper
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US3170809 *May 4, 1962Feb 23, 1965Oxford Paper CoTransfer sheet and process of making
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3432376 *Jan 28, 1964Mar 11, 1969Letraset International LtdDry transfer sheets and processes for using the same
US3510385 *Aug 2, 1966May 5, 1970Letraset International LtdDry transfer assembly
US3516904 *Apr 7, 1966Jun 23, 1970Diamond Int CorpHeat transfer decalcomania for application to plastic bottles made from a laminate of a polyamide adhesive,a printed layer,and a wax like heat release layer
US3847725 *Nov 28, 1969Nov 12, 1974Avery Products CorpDry transfer materials
US3896249 *Apr 4, 1973Jul 22, 1975Johnson Matthey Co LtdSelf-adhesive transfers
US3900586 *Dec 20, 1972Aug 19, 1975Australia Res LabElectrostatic duplicating process
US3924026 *Jan 28, 1974Dec 2, 1975Henry S PenfieldImage preservation and transfer process
US3928710 *Jul 10, 1973Dec 23, 1975Letraset International LtdHeat activated transfers
US3930921 *Aug 13, 1973Jan 6, 1976Barrett & CompanyThermoplastic adhesive acrylic layer
US3940864 *Mar 25, 1974Mar 2, 1976Contemporary, Inc.Plastic plates adapted to be imprinted and methods of manufacturing and imprinting on plastic plates
US4068028 *Jun 9, 1971Jan 10, 1978Unical CorporationApparatus and method of producing transparent labels with printing on the adhesive and product produced thereby
US4171785 *Jun 30, 1977Oct 23, 1979The Boeing CompanyApparatus and method for manufacturing laminar flow control aircraft structure
US5573865 *May 24, 1995Nov 12, 1996Minnesota Mining And Manufacturing CompanyGraphics transfer article
US5681631 *Feb 14, 1995Oct 28, 1997Minnesota Mining And Manufacturing CompanyOverlay composites
US5851614 *Dec 10, 1996Dec 22, 1998Buck; Ronald MarkSelf-adhesive opaque dry transfer decals
US5852121 *Jun 9, 1997Dec 22, 1998Minnesota Mining And Manufacturing CompanyElectrostatic toner receptor layer of rubber modified thermoplastic
US6254970Oct 8, 1998Jul 3, 2001International Playing Card & Label Co.Ink and adhesive lacquer of heat activated polyester formed on transfer release agent; packages
US6322874May 24, 1995Nov 27, 20013M Innovative Properties CompanyBlend of an acrylic resin, a vinyl resin, a solution or dispersion grade rubber and a plasticizer; adhering to a first major surface of a crack resistant film; durability and flexibility
EP0279986A1 *Dec 8, 1987Aug 31, 1988Alza CorporationSkin permeation enhancer compositions using glycerol monolaurate
WO1979000103A1 *Jul 10, 1978Mar 8, 1979Stauffer Chemical CoMetallized decorative film laminate and process
Classifications
U.S. Classification156/230, 156/249, 428/914, 524/733
International ClassificationB44C1/17
Cooperative ClassificationB44C1/1741, Y10S428/914
European ClassificationB44C1/17H4