|Publication number||US3079351 A|
|Publication date||Feb 26, 1963|
|Filing date||Nov 26, 1958|
|Priority date||Nov 26, 1958|
|Publication number||US 3079351 A, US 3079351A, US-A-3079351, US3079351 A, US3079351A|
|Inventors||Bernard J Staneslow, Macaulay Norman|
|Original Assignee||Moore Business Forms Inc|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (9), Referenced by (36), Classifications (11)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 3,079,351 CQPYEIJG MATERHALS AND EMULSHONS Bernard J. Staneslow and Norman Macaulay, Niagara Falls, N.Y., assignors to Moore Business Forms, ind, Niagara Falls, N.Y., a corporation of Delaware 'No Drawing. Filed Nov. 26, 1958, Ser. No. 776,407 21 Claims. (Cl. 26li3) The present invention relates to a novel process for producing novel pressure-sensitive record or copying material and to the material thereby produced. The invention further relates to novel hot-melt emulsions for producing the novel pressure-sensitive record material of the invention.
The pressure-sensitive record or copying material which is still predominantly used in commerce today is the transfer paper commonly referred to as carbon paper. Such ordinary carbon paper usually consistts of paper coated with a homogeneous mixture of waxes and oils with a coloring material uniformly and homogeneously dispersed in the mixture. This homogeneous coating is generally applied to the surface of the sheets as a hot melt or molten mass. The resulting pressure-sensitive record material provides a mark under the pressure of writing, typing, etc. by transfer, at the areas of pressure, of a complete mass of the coating composition containing the color therein. In order to provide a reasonable degree of transfer when a copy is produced, the waxy con position which is transferred is, of necessity, relatively soft and of low tensile strength. The coating is, therefore prone to sent? or offset onto adjacent objects, including an adjacent sheet of clean paper. Furthermore, the mark or copy produced is prone to smudge on the receiving sheet and also to ofl'set onto the hands and clothing of the user.
Because of the shortcomings of ordinary carbon paper, a great deal of research effort has gone into the search for a more suitable copying material. One of the attempts to solve the shortcomings of carbon paper has employed a colorless dye intermediate which reacts to form a color only when brought into contact, with sufficient pressure, with a suitably prepared receptive sheet containing a reactant which will react with the colorless dye intermediate to form a colored image or marking. It was hoped that the use of the colorless marking materials would help in eliminating the offset which normally occurs with ordinary carbon paper.
However, to produce a sufliciently rapid development of color on the clay surface of the receiving sheet of such a system, very rapid adsorption of the dye interme diate into the clay surface is required. For this purpose, rapid migration of the dye intermediate to the clay surface from the transferred mass must take place and this could only be achieved in part by incorporating an excessive amount of solvent for the dye intermediate into the wax coating mixture. Consequently, the transfer mark or character was even more prone to smear than that produced with a good quality ordinary carbon paper. Since manifold systems employing sheets of transfer material require that the transfer surface be placed in contact with the receptive reactive surface over relatively long periods of time during storage, oiiset and un wanted production of color on the receptive sheet frequently occurred. In such a system, this difficulty could not easily be overcome. Consequently, in a manifold system, record sheets of this type, utilizing a colorless dye intermediate, possessed only the advantage that the dye intermediate did not form color on the hands and clothing of the user.
Over the years, efforts have been directed to a further type of pressure-sensitive copying material which employs, on one side of a sheet, a continuous coating containing discrete inclusions of a marking fluid. This type of system employs as the coating, a continuous film containing microscopic droplets of an oily marking material and is the type of system described in British Patent No. 392,220, United States Patents Nos. 2,299,694 and 2,374,862. In this type of copying sheet, the marking fluid may be colored, or it may be colorless but capable of forming a color upon chemical reaction with another chemical deposited on the contacting surface of the adjacent sheet. Under the pressure of writing or typing, the coating ruptures and droplets of marking fluid exude onto the copy sheet to provide a mark by direct color transfer or due to the color-forming chemical reaction which takes place between the co-reacting chemicals.
While this latter type of pressure-sensitive copying material provided certain advantages, it did not overcome all of the disadvantages of ordinary carbon paper. Furthermore, it brought about new disadvantages such as time-consuming, costly production operations and handling problems, with resulting high prices to the users which, in turn, have caused its commerecial use to lag.
By means of the present invention it is possible to overcome all of the diificulties of the prior systems mentioned hereinabove, and to provide pressure sensitive copying materials which are superior both in their properties and performances, and which may be efficiently and inexpensively produced.
it is an object of the present invention to provide a superior pressure sensitive copying material which eliminates the disadvantages of ordinary carbon papers as well as those of prior art copying materials, while retaining their better characteristics.
It is also an object of the present invention to provide a clean, non-smudging pressure-sensitive copying material Which eliminates staining and offsetting of color on to a contacting copy receiving sheet and which provides a copy which does not smear, stain or offset by virtue of the fact that the marking fluid which provides the copy is absorbed into the receiving surface of the copy sheet.
it is also an object of the present invention to provide a pressure-sensitive copying material having a continuous iupturable coating of a film-forming material meltable Within the range of -350 F. and containing dispersed therein discrete droplets of a non-viscous marking fluid which is capable of being exuded from the coating under writing pressure, to give a mark on an adjacent receiving surface, and which has superior copy writeoff intensity for both multiple as well as one-time use.
It is an additional object of the present invention to provide a pressure-sensitive copying material in which the non-viscous marking fluid is dispersed as discrete droplets throughout a scufi-resistant, non-transferable coating which is insensitive to drying out or humidity conditions and not subject to cracking with premature release of the marking fluid.
It is another object of the invention to provide stable emulsions of a non-viscous marking fluid dispersed as microscopic discrete liquid particles in a continuous phase of non-aqueous molten fluid composition, said dispersion of microscopic discrete liquid particles of marking fluid not being subject to coalescence on storage of the composition or during repeated solidification and remelting cycles.
Another object of the invention is to provide a molten coating composition readily applied to a web such as paper by conventional coating and printing equipment and methods, and which does not require the removal and/or recovery of volatile solvents or water.
The above enumerated objects, as well as other objects, together with the advantages of the invention, will be readily comprehended by persons skilled in the art upon reference to this description;
The pressure-sensitive record material of the present invention consists of a Web support, such as paper, having coated on at least a portion of a surface thereof, a continuous film of a rupturable material meltable within the range of 130350 F. and containing dispersed therein, In roscopic discrete droplets of a non-viscous marking fluid such that, under pressure of pencil or machine writing, the film is ruptured and the marking fluid exuded to mark ah adjacent receiving sheet. This pressure-sensitive coating is characterized by being applied to the paper as a stable dispersion of marking fluid droplets in the molten 100% solids continuous phase and chilled thereon.
H Throughout the present application the term emulsion refers to a dispersion of marking fluid in the molten material of the continuous phase, regardless of whether or, not the marking fluid has been encapsulated in a protective shell previous to dispersion in the continuous phase. v
Themarkin'g fluid may be colored or colorless. It color1ess, it will form a color upon color reaction with a cd-reac'tant on an adjacent contacting sheet. I
The fluid of the marking fluid must be substantially insoluble in the film-forming material or the continuous Pha e.
Under pressure of Writingand typing, the film of the coating i sr'uptured and the marking fluid, by virtue of its iron-viscous nature, is exuded to give a mark on a reeeiving sheet. In the case of the marking fluid being colored, the receiving sheet may be just an ordinary sheet of paper into which the color fluid is absorbed. Inthe case 'of the marking fluid containing a color-forming dye intermediate, the receiving surface contains, impregna ted or coated thereon, the co-reactant necessary toproduce color by reaction with the exuded marking fluid.
Under the writing pressure, the marking fluid only is transferred to the receiving sheet, the film of the coating being of a nature such that no transfer of the film to the receiving sheet takes place. The mark on the receiving sheet is produced by absorption of the marking fluid into the surface of the receiving sheet and thus presents no surface deposit which might be susceptible to smudgin'g as in the common transferable Wax type of carbon paper and the transferable wax sheets of the prior art. In the coated sheet of the present invention, the markingfluid droplets are occluded within the film at the coating and the actual fluid is protected from confact "with hands and clothing and does not come into contact with thereceiving sheet until such time as the film is ruptured during the process of producing a copy. Thesurfaceof the coated sheet is, therefore, clean and non-'smud'ging. This cannot be said of the coatings utilizing nomo enous wax compositions, as the surface material in these coatings constitutes part of the transferable marking medium and is very susceptible to smudging, staining and ofisetting on contact with hands and the receiving sheet. v e
In previous copying materials coated from solvent solutio'ns, there has beenlittle control of droplet diameter,
and inadequate occlusion of surface droplets by these methods has resulted in the occurrence of very marked bleeding or marking fluid from the surface of such coating. Because of the preformed emulsion system utilized in the present invention, droplet size is uniform, and occlusion of surface droplets is much more complete, and insures cleanliness and negligible bleeding characteristics.
Emulsion systems which are necessary to give clean, non bleeding characteristics in coatings, have heretofore been confined to hydrophilic colloid materials because at their natural tendencies to stabilize aqueous emulsions. pnfortuna't'el'y, coatings prepared from these materials tend 't'o'c'rack and give unsatisfactory results because of the premature release of the marking fluid through the cracks which form.
The advantages of using film-forming materials other than humidity-susceptible, water-soluble, hydrophilic colloids in emulsion coatings are obvious, but the use of non-aqueous film formers has'previously been excluded because of the difliculty of preparing suitable nonaqueous emulsions. The present invention provides stable non-aqueous emulsions having excellent coating properties.
The greater proportion of copying and-record materials are presently manufactured by processes involving hot melt methods, and aqueous coatings are not readily adapt able to this equipment. Since the equipment required to process aqueous coatings is not generally utilized by manufacturers of, for example, manifolding business forms, the coated stock has generally to be brought in from an outside source. This involves the disadvantages of extra shipping and handling and burdensome inventories. The excessive handling particularly undesirable in pressure-sensitive systems wherein a colorless colorfor'rning dye intermediate is coated on one side of a paper and the receptive coating necessary to produce color is applied to the opposite side of the paper. It has been found that such sensitive paper is difiicult to supply in tight rolls and that the rolls require special handling to overchome premature offset. In addition, even with special precautions, waste of precoated materials during fabrication of such products as business forms, is excessive.
In order to minimize offsetting of the copying material, it is advantageous to the manufacturer of manifolding business forms to be able to apply the pressure-sensitive coating at the press at a location after the printing, punching, perforating, and slitting operations have taken place.
Water based coatings utilized in this manner are not feasible with the equipment presently used in the carbon coating and printing industry and to be of utility, it would be necessary either to install additional costly equipment or to obtain precoated materials from an outside source. In the latter case, the versatility and flexibility of manufacturing operations are considerably reduced but, in either case, costs are considerably higher.
One of the advantages of the copying material of the present invention is its direct utility on existing production equipment without additional limitations in manufacturing flexbility. One of the important contributing factors which made possible the advantages of the product of the invention is the nature of the continuous phase of the coating. The emulsions from which these coatings are produced will be described in greater detail hereinbelow.
The continuous phase of the coating and the emulsion comprises a hydrophobic film-forming material, which is in the solid state at ordinary temperatures at which the copying material is to be used and mel'table without decomposition at elevated temperatures up to about 350 F., and preferably between about and 320 F. This is one of the essential characteristics of the film-forming material. It is this characteristic which permits the application of the coating to paper employing a hot-melt technique.
The hydrophobic film-forming material of the continuous phase may consist of one or more components selected from a wide variety of materials, satisfying the conditions of thermoplasticity mentioned above. Generally, materials which give low viscosity and low coating temperatures are most desirable from the point of view or application case. However, the use of high melting, high viscosity polymers is not excluded from the scope of the invention since coatings having such materials as the main or sole constituent of the continuous phase can readily be coated on paper by extrusion methods, similar to the extrusion of sheet plastics.
Among the hydrophobic materials which can be used to produce the continuous phase, either singly or in com bination, are the thermoplastic acrylic resins, such as polymethyl methacrylate and its copolymers; cellulose derivatives, such as ethyl-cellulose and cellulose acetatebutyrate; coumarone-indene resins; petroleum hydrocarbon resins such as the Piccopale resins (thermoplastic hydrocarbon resins derived from high temperature cracking of petroleum consisting of a mixture of straight chain hydrocarbon resins in which considerable cyclic, but no aromatic structures, are present); isobutylene resins, such as poly-isobutylene; phenolic resins, such as Durez 219 (a terpene, phenolic, oil soluble thermoplastic resin having a melting point of about 270 F. and an acid number of about 65); polyamide resins, such as alkoxy sub stituted nylon; chemically modified rubbers, such as cyclized rubber; styrene resins, such as polystyrene; terpene resins, such as Piccolyte resins (a terpene polymer having a molecular weight of approximately 1200, a softening point of about 115 C., and a density of 15.5 C. or 0.980); vinyl resins, such as polyvinylacetate, and vinyl stearate and copolyrners; natural and synthetic waxes such as the vegetable waxes, candelilla (a hard vegetable wax composed of a high proportion of hydrocarbons and resins with a small amount of lactones, a melting point of 145 162 R, an acid number of 11-49, a saponification number of 4656 and a specific gravity of 0.982 to 0.993 at 15 C.), carnauba, and sugar cane waxes, hydrocarbon waxes such as parafiin, ozokerite, and microcrystalline waxes, mineral waxes such as montan and Utah wax (an amorphous mineral wax from Utah having a melting point of 73 C., a cloud point of 76 C. and an acid number of 0), synthetic waxes such as polyethylene and FT-ZOO wax (a synthetic mineral wax having a melting point of 2l2219 F., a saponiiication value of less than 0.5 and an acid value of 0) prepared by the Fischer-Tropsch process, and also chemically modified natural waxes such as chlorinated parafilns and oxidized microcrystalline waxes. The above materials are hydrophobic in nature, but hydrophilic materials may also be used. For example, polyethylene glycols which are solids at temperatures of normal usage, but meltable at temperatures between about 130 F. and 350 B, may be used. Thus, polyethylene glycol, molecular wt. 6000- 7500, melting point 140145 F., is suitable.
By dissolving those materials of high melting point and viscosity in the lower melting point materials such as the waxes, compositions have been obtained of excellent coating viscosity for carbon paper coating equipment yet possessing some of the properties of the higher melting constituent.
Although the addition of surface-active agent or protective colloid to the continuous phase composition generally enhances the stability of the emulsion or dispersion, excellent results have been obtained in accordance with the present invention, employing a wax such as candelilla as the sole component of the continuous phase with no emulsifying agent. As will be apparent to those skilled in the art, other waxes possessing a melting point above about 130 F. and less than about 350 F. may be employed.
One valuable addition to the continuous phase is a cyclized rubber resin. This resin imparts toughness to the coating film on the paper while also providing the important function of being an efiicient emulsion stabilizer. As little as 3% of this resin in a coating having paraffin wax as the sole component of the continuous phase, produces an emulsion of excellent stability otherwise unobtainable. Examples of this resin are Alpex resin and Pliolite resin. The latter resin may be produced by reacting rubber in solution with an amphoteric halide or chlorostannic acid and isolating the resulting cyclized resin. This resin is substantially a condensation derivative of rubber and its preparation is described in U.S. Patent No. 2,052,391.
One preferred continuous phase of the emulsion of the invention comprises one or more thermoplastic polymeric resins having a melting point of between about 130 and 350 F., constituting between about 25 and by weight of the film-forming material, between about 10 and 75% by weight of one or more hydrophobic waxes and between about 1 and 10% and preferably between about 2 and 5% by weight of a cyclized rubber resin.
The proportions of marking fluid containing the pig ment, dye, or dye intermediate, relative to the amount of film-forming component may vary over a wide range, depending upon the materials used. Best results have been obtained employing the marking fluid in an amount of between about 20 and 60%, preferably between about 35 and 50%, by weight of the total emulsion or coating composition.
The microscopic discrete liquid particles of the nonviscous marking iluid in the coating are desirably solutions or suspensions of a dye, pigment, or colorless colorforming dye intermediate in a liquid which is inert to and substantially insoluble in the molten continuous phase.
The marking fluid may comprise any non-viscous liquid, whether organic or inorganic, of such polarity as to render it substantially insoluble in the hydrophobic film-forming composition, which will provide a suspending or dissolving medium for the pigment, or colored dye or colorless color-forming dye intermediates. The non-viscous liquid should not be too viscous since it is important that it be able ot accommodate the pigment or dye without becoming so viscous as to lose its freefiowing characteristics. Desirably, the fluid medium (solvent or suspending liquid) shall have a low volatility, i.e., wherein less than about 10% of the liquid evaporates through the continuous film over a period of several years of normal storage. Liquids having vapor pressure of less than 0.01 mm. of mercury at 75 F. are particularly satisfactory in this respect. Additionally, the fluid shall desirably have a low freezing point, i.e., a freezing point of less than 0 F., preferably as low as 30 F. Also, the fluid shall desirably have a high boiling point which will provide reduced volatility at temperatures of use. Fluids having boiling points in excess of 212 F. are usually suitable in this respect. An additional important property of the fluid is that it have a flash point above the manufacturing temperatures. Fluids having a flash pointabove 212 F. are generally satisfactory. As those skilled in the art will appreciate, the product will be more useful, permanent and safe With liquids having higher boiling points and flash points and lower volatility and freezing points. Of course, as mentioned hereinabove, the fluid must not dissolve, or by encapsulation is prevented from dissolving, the film-former. Among the satisfactory fluids which may be employed are those listed below in Table l:
It is important that the marking fluid be of a nonviscous nature to permit it to exude readily from the coating of the copying material when subjected to writing pressures. Viscous or pasty fluid droplets, and par ticularly if the fluid comprises a small part of the coating, will not exude from the coating when subjected to writing pressure. Under such circumstances, instead of exuding, the marking fluid is transferred to the copy sheet together as a unit of the entire coating thereby causing copy smudging as is typical with ordinary carbon papers. To permit the marking fluid to exude from the coating without any transfer of coating fllm itself, it is desirable that the marking fluid have a viscosity of less than about 50,000 centipoises at 70 F., preferably between about 30 and 30,000 centipoises at 70 F., and for best results between about 50 and 5,000 centipoises at 70 F.
Another important feature which provides excellent exudation'of the marking fluid is to employ a coating emulsion containing substantial amounts of the marking fluid. It is generally advantageous to employ a coating emulsion containing at least about 20% up to about 60%, and preferably about 35 to 50%, by weight of marking fluid, based upon the total weight of coating emulsion.
The marking fluid may contain various amounts of solvent or suspending liquid depending upon the nature of and'amount of pigment or dye, the nature of the solvent or suspending liquid, and somewhat upon the nature of the film-forming or continuous phase of the coating emulsion.
The marking fluid may contain a colored pigment or dye or it may contain a colorless color-forming dye intermediate which will react to produce a color when brought into contact with a co-reactant. The line of demarcation between pigments and dyes is often diflicult to delineate. 'As used herein, a pigment is considered to be a colored or colorless color-forming substance which is insoluble in the fluid of the marking fluid.
A dye is herein considered to be a colored or colorless color-forming substance which is soluble in the fluid of the marking fluid.
Colored substances which may be employed include materials normally classified as pigments such as carbon blacks, iron blues, alkali blues, phthalocyanines, cadmium reds, uitrarnarine blues, phosphoand molybdotungstic acid laked colors; and materials normally classified as dyes such as di and tri-aryl methane dyes, e.g., malachite green and crystal violet, azo dyes, indigoid, thioindigoid and anthraquinone dyes, acridine, azine, oxazine, and thiazine dyes.
Among the usable color-forming dye intermediates are: stabilized diazonium salts, the carbinol, leuco and ether derivatives of the triaryl and diarylmethane dyes, and acid esters of leuco indigoid and thioindigoid dyes. Examples of suitable intermediates of diand triarylmethane dyes which may be employed are the butylethers of methyl violet 2B, methyl violet 10B, magenta, malachite green A, auramine derivatives such as N-acetyl auramine and leucoauramines.
One type of colorless color-forming dye system which may be advantageously employed in the copying products' 'of the invention is that described in British Patent No. "757,136. In accordance with that patent a colorless color-forming dye intermediate, such as an ether of a triphenylmethane dye-former is maintained in an alkaline condition by neutralizing the dye former with an alkaline substance, in which form the dye-former is colorless, and then producing a color by bringing the alkaline colorless'dyestuff into contact with an excess of an acid which converts the dye-former into a colored product. In accordance with one embodiment of the present invention the marking fluid may contain the colorless color-forming dye intermediate along with a small amount of a'nalkaline substance, such as sodium carbon ate, potassium hydroxide, organic alkali, etc.
In a manifolding set-of record forms, the emulsion containing the marking 'fluid' is coated on the back surface of *the'ssheets so that the coating can come in contact with the front surface of the sheets which follow the first sheet in the set. On the front surface of the sheets is placed a co-reactant for the dye intermediate. in order to produ ce a color.
Among the co-reactants which may be used in the coating composition for the front surface of the sheets are acids such as: tannic, gallic, citric, boric, tartaric, oxalic, and phospho-tungstic acids. Also one may employ other co-reactants such as: colloidal silicas, calcium silicate, attapulgite clay, and the like.
As will be apparent to those skilled in the art, from the teachings of this disclosure it is possible to incorporate the co-reactant into the marking fluid of the emulsion on the back surface of the sheets and to place the colorless color-forming dye intermediate on the front surface of the sheets. In either instance when pressure is exerted through two or more sheets in the manifolding set, rupture of the continuous film will produce intermixing of the reactive chemicals to produce a color or copy at the sites where pressure is applied.
Coatings weighing 1 to 12 lbs. per 500 sheets of 20 inch x 30 inch paper in which 20 to 60 percent of the weight of the coating consists of marking fluid have been found to be satisfactory. For one time use coatings, a desirable weight range is from 1 to 6 lbs., preferably 2 to 4 lbs., and for multiple use coatings, a desirable weight range is from 6 to 12 lbs., preferably 8 to 10 lbs. In addition to single-face coatings, double face coatings are desirable for certain uses.
The discrete microscopic particles of marking fluid contained in the coating and emulsion are desirably of from between about 0.1 and 70 microns in diameter. More desirably, the diameter of the liquid particles is from about 0.5 to 20 microns. For preferred results, it has been found that a droplet diameter of between about 1 and 5 microns is most satisfactory. When the particle size exceeds 20 microns in diameter, a coating containing the droplets on a paper surface may become slightly dirty to the touch because the diameter of the droplets is about the same as the thickness of the coating which is therefore easily broken. Below a diameter of one micron, the coating is less sensitive to rupture when subjected to the pressure employed to produce copying. Since it is desired to employ the coating of the invention in pressure-sensitive copying systems which do not require the use of excessive pressure, it is desirable to provide droplets having a diameter of from about 1 to 5 microns.
As will be appreciated by those skilled in the art, the sensitivity to rupture under pressure is dependent upon the size of the droplet as well as the nature of the film, with the large size droplets having greater tendency to rupture when subjected topressure than the smaller size droplets. The discontinuous phase of the emulsion shall constitute the marking fluid which comprises the pigment, colored dye or colorless color-forming dye intermediate suspended or dissolved in a non-volatile liquid. Emulsions are produced by placing the two mutually insoluble liquids in a blender or emulsifier and by agitation producing a stable emulsion with droplets of marking fluid of the desired particle size, desirably less than about 10 microns, and preferably 1 to 5 microns in diameter. The resulting emulsion can then be applied to paper by the standard coating or printing methods; such as, letter press, direct or offset gravure, direct or reverse roll, knife, flexographic, etc.
Among the important advantages of the emulsion coatings of the invention is the extreme flexibility and versatility in the manner in which they may be applied to web material, such as paper. These emulsion coatings are particularly satisfactory since they provide an excellent means of hot-melt spot application whereby prescribed areas on the backs or fronts of the sheets of paper may be coated.
In order more clearly to disclose the nature of the present invention, specific examples illustrating the practice of the invention will hereinafter be described. It should be understood, however, that this is done solely by way of example and is intended neither to delineate the scope of the invention nor limit the ambit of the appended claims. The amounts of components are given in terms of parts by weight, unless otherwise specified.
Example 1 This example describes the preparation of a preferred copying sheet according to the invention coated with a film comprising a continuous phase of a blend of cyclized rubber resin, polyterpene resin and a paraflin wax mixture, which film has disposed therein microscopic discrete liquid particles of a marking fluid containing a colored dye.
A molten mixture having a temperature of 240 F. was prepared by mixing together and heating 180 parts of Schenectady resin ST-S 115 (a polyterpene resin made from pinenes having a melting point of about 239 F.), 70 parts of FT-200 parafiin wax (a synthetic high molecular weight aliphatic hydrocarbon wax having a melting point of 210-214 F. and having a molecular weight of about 750 corresponding to a long hydrocarbon chain containing about 50-55 carbon atoms per molecule, produced by the Fischer-Tropsch process), 50 parts of microcrystalline paraffin wax (Warco 180, a hard, brittle, white microcrystalline petroleum wax having a melting point of 180185 R, an acid number of 0, a saponification number of 0), 65 parts of paraffin wax having a melting point of 135 F., and 20 parts of cyclized rubber resin (Alpex resin). The resulting mixture, having its temperature maintained at 240 F., was passed through a homogenizing mill and was then mixed with a solution of 28 parts of crystal violet dye dissolved in 257 parts of polyethylene glycol having a molecular weight of 400. The solution of the dye in polyethylene glycol had a viscosity of 156 centipoises at 70 F. when measured on the Brookfield viscometer using the No. 2 spindle at a speed of 60 rpm. Homogenization by passing the hot mixture through the homogenizing mill was then continued for 3 minutes thereby providing an excellent stable emulsion of liquid dye-containing particles of 1-10 microns diameter uniformly dispersed in the wax and resin base. The resulting emulsion was stable over a period of 72 hours while maintained in the molten condition at 240 F. Upon solidification and remelting at 240 F., with stirring, no separation of the emulsion could be observed.
The molten emulsion (at a temperature of 240 F.) was coated on paper, the excess being removed by means of a doctor bar to provide a coating weight of 3 pounds per 500 sheet ream of paper of 20 inches by 30 inches size. The discrete fluid particles of marking liquid were retained in the coating upon cooling. The resulting coated sheets provided excellent copying paper when used in the manner that ordinary carbon paper is used. The copying paper possessed excellent cleanliness and nonsmear characteristics, with little ofiset. Copies made with this paper were characterized by a strong color, good definition and legibility and excellent resistance to smudging.
Example 2 This example describes the preparation or" a copying system according to the invention in which the backs of sheets of paper are coated with a film comprising a continuous phase of a blend of cyclized rubber resin, polyterpene resin and a hydrophobic paraflin wax containing microscopic discrete liquid particles of a marking fluid containing a colorless color-forming dye intermediate capable of forming color upon reaction with an acidic material.
About 65 parts of Schenectady resin ST-5l15, 45 parts of FT-200 paraflin wax and 5 parts of cyclized rubber resin (Alpex resin) were mixed and melted together by heating them to a temperature of 240 F. A solution of 5 parts of p-phenylleucoauramine dissolved in parts of polyalkylene glycol (Ucon LB1145, a polyalkylene glycol having a viscosity index of 137, a pour point of 20 F., a flash point of 430 F. and a density at 60 F. of 1.003) containing 2 to 3 drops of ethanolamine was heated to 240 F. and added with rapid agitation to the mixture of resins and wax which had also been maintained at a temperature of 240 F. until a finely dispersed stable emulsion was formed. This emulsion was. spot printed onto the backs of sheets of paper by a flexographic process to provide sheets of paper having certain areas coated with the colorless, color-forming coating. When these sheets were in register with an adjacent receptive surface of paper coated with an acidic material, such as tannic acid, or other co-reactants such as calcium silicate, and the writing pressure applied to the copying sheet, the liquid discrete particles of colorless color-forming marking material exuded from the emulsion coating onto the adjacent receptive surface to provide a blue mark. Copies made with this paper were characterized by strong color, good definition and legibility and excellent resistance to smudging or offset.
Example 3 This example describes the preparation of a preferred copying sheet according to the invention in which the discrete liquid particles of marking fluid contain a colored pigment.
About 25 parts of iron blue pigment were dispersed in parts of polyethylene glycol having a molecular weight of about 400. This dispersion had a viscosity of 456 centipoises at 70 F. when measured on the Brookfield viscometer using a No. 2 spindle at 60 rpm. A molten mixture was prepared by mixing and heating together at a temperature of 240 F., 65 parts of Schenectady resin ST-S 115, 45 parts of FT-200 paraflin wax and 5 parts of cyclized rubber resin (Alpex resin). Into the molten mixture of resins and wax, was emulsified by violent agitation, parts of polyethylene glycol (mol wt. 400) marking fluid containing the iron pigment. The resulting molten emulsion, maintained at a temperature of 240 F. was applied to the backs of sheets of paper. The resulting copying paper provided excellent copying when used in the manner that ordinary carbon paper is used. It was characterized by excellent cleanliness and resistance to smearing and produced very little offset. Copies made with this paper possessed a strong color, excellent definition and legibility, and resistance to smudging.
Example 4 This example describes the preparation of a copying sheet in accordance with the invention coated with a film comprising a continuous phase of a polyterpene resin which film has disposed therein microscopic discrete liiquid particles of a marking fluid containing a colored A melt having a temperature of 240 F. was prepared by heating 385 parts of Schenectady resin ST5115, 20 parts Alpex resin and 100 parts 100 second Saybolt mineral oil. This melt at a temperature of 240 F. was then mixed with a solution of 15 parts of crystal violet dye dissolved in parts of polyethylene glycol having a molecular weight of 400. The dye solution had a viscosity of 156 centipoises at 70 F. when measured on the Brookfield viscometer using a No. 2 spindle at a speed of 60 r.p.m. Homogenization by passing the hot mixture through the homogenizing mill was then continued for 3 minutes thereby providing an emulsion of liquid dye-containing particles of 110 microns diameter dispersed in the resin base.
The molten emulsion (at a temperature of 240 F.) was coated on paper, the excess being removed by means 11 of a doctor 'barto provide a coating weight of 3pounds per 500 sheet ream of paper of 20 inches by 30 inches size. The discrete fluid particles of marking liquid were retained in the coating upon cooling. The resulting coated sheets provided excellent copying paper when used in the manner that ordinary carbon paper is used.
Example 5 This example describes the preparation of copying sheets in accordance with the invention coated with a film comprising a continuous phase of cyclized rubber resin and paraffin wax, which film has disposed therein microscopic discrete liquid particles of marking fluid containing a colored dye.
About 3.0 parts of cyclized rubber resin (Alpex resin) was dissolved at 200 F. in 54.3 parts of a close-cut paraflin wax having a melting point of 155 F. (5512 wax, a close out parafiin wax having a melti g point of 153 F., a penetration value of at 77 F., and a specific gravity at 60 F. of 0.928),. crystal violet dye in 38.5 parts of polyethylene glycol- (molecular wt. 400) at 200 F. was. homogenized into the wax solution and the resulting emulsion coated at 180 F. on to 9 lb. carbonizing tissue to give a coating weight of 2 /2 lbs., ",x 3050 0 sheet ream. The resulting coated sheets provided excellent copy and manifolding qualities when used as a copying paper.
Example 6 This example describes a hot melt emulsion system in accordance with the present invention employing a colored dye in the marking fluid.
A melt was prepared at 200 F. of 35.7 parts Sun Wax 5512, 9.7 parts oxidized microcrystalline wax having amelting point of l95200 F. (Cardis I, an emulsifiable oxidized petroleum wax having a melting point of 195- 200 F., a penetration value of 1 to 2, an acid number of 12 to 16, and a saponification number of 55 to 65), 3.0- parts Alpex resin and 9.0 parts natural hydrocarbon resin (Parco #200 resin, a natural fossil hydrocarbon resin having an average molecular weight of about 732, a softening point of 160-170 C., an acid number of 68,v an iodine value or 140-150 and a specific gravity of 1.03 to 1.06). A solution of 4.2 parts of crystal violet dye in 38.4 parts of polyethylene glycol (molecular weight 400). (the solution having a Brookfield viscosity of 156.- centipoises at 70 F.) was slowly added to the wax mixture at 200 F. with rapid agitation in a Kady- Mill. An excellent hot-melt emulsion was produced of very uniform size distribution between 1 and. 10 microns diameter. When coated on paper, an excellent copying paper resulted.
Example 7 This example describes a copying system of the invention employing coating having a continuous phase of a polyethylene and wax blend.
About 3.0 parts Alpex resin, 12.6 parts polyethylene resin (grade 629, a low molecular weight emulsifiable grade of polyethylene having a melting point of 208212 R, an acid No. of 14-17 and a saponification No. of 14 17) and 4.5 parts sugar cane wax and 37.5 parts Sun Wax 5512 were melted together at 205 F. To this mixture was added at 205 F. a solution of 4.2 parts crystal violet dye in 38.4 parts polyethylene glycol 400 (the solution having a Brookfield viscosity of 156 centipoises at 70 F.) and the emulsion so formed agitated thoroughly. An excellent stable low viscosity emulsion was obtained which coated well at 205 F. on 9 lb. carbonizing tissue by a scrape bar method. An excellent copying paper resulted giving an intense mark on a copy paper.
Example 8 This example describes the preparation of a preferred copying material according to the invention coated with a film comprisinga continuous phase of a blend of cyclized' A. solution of 4.2 parts rubber resin, a resin and a hydrophobic paraflin wax, which film has disposed therein microscopic discrete liquid particles of a colorless marking fluid containing a colorforming dye intermediate.
About 7 parts of colorless methyl violet carbinol were dissolved in a mixture of 50 parts of ethoxytriglycol, 50 parts of polyethylene glycol having a molecular weight of 400, and 2 parts of sodium hydroxide. The resulting solution had a viscosity of 47 centipoises at 70 F. when measured on the Brookfield viscometeremploying a No. 2. spindle at a speed of 60 rpm. The resulting solution was emulsified by rapid agitation into a molten mixture prepared by mixing and heating together at 240 F., 360 parts of PT-200" parafiin wax, 21 parts of coumaroneindene resin having a melting point of 185 F. ('Piccopale and 70 parts of cyclized rubber resin (Pliolite N The resulting molten emulsion was coated ontothe backs of sheets of paper and upon cooling-provided a copy material having colorless fluid inclusions of I marking fluid microscopically dispersed throughout the continuous coating of themixture of'resins and wax. The same sheets of paper were treated on the front surfaces with tannic acid. When these sheets were collated in manifold form, with the tannic acid treated surfaces in. contact with the colorless coating, and writing pressure applied to the front of the top sheet, a copy was produced on the fronts of all the sheets in the manifold. Copiesmade. with this paper were characterized by strong, color, Substantially no offset,v good definition and legibility and excellent resistance to smudging.
Example 9 This example describes the preparation of 9. copying; material employing Candelilla. wax as the film-former of the paper coating.
About 8 parts of crystal violet dye were dissolved in- 92 parts of thiodiethyleneglycol. The resulting solution had a viscosity oi 75 centipoises. at 7 0 F. when measured. on the Brookfield viscometer employing a No. 2 spindle at a speed of 60 r.p.m. 25. parts of the resulting solution was heated to 175 F. and mixed with parts of Candelilla wax molten at a temperature of F. with rapid agitation in a Kady ill for 10 minutes. The resulting emulsion contained microscopic discrete fluid inclusions of the. crystal violet dye solution dispersed throughout the continuous phase of Candelilla wax; The resultant. molten emulsion was coated onto one side of the sheets of paper and the excess removed with a doctor blade after which the coating was set by passing the, coated paper over cold rollers. Thev copying material thus prepared provided excellent write-oil properties and was much freer of offset and smudging than ordinary carbon paper.
Example 10 This example describes the preparation of copying sheets. according to the invention in which both the continuous. phase and the dispersed phasev are Water insoluble.
A dye solution was prepared by dissolving 28 grams of crystal violet dye into 257 grams polyepichlorohydrin of molecular weight 450 (Poiyglycol 166-450). A melt was prepared at 200 F. of 300 grams paraflin wax (#5512 wax), 65 grams Cardis I wax, and 25 grams Alpex resin. The dye solution at 200 F. was added to this melt at 200 F. with vigorous agitation in a Waring Blender. After homogenizing for 3 minutes at high speed, the resulting emulsion was coated at 200 F. by a gravity method onto 9 lb. Champlain carbonizing tissue to give a coating weight of 3 lbs. for a 500 sheet ream of sheets 20 inches by 30 inches.
As will be apparent to those skilled in the art other marking fluids, dyes, pigments and film-formers may be employed within the concept of the present invention.
The terms and expressions which we have employed are used as terms of description and not of limitation, and
13 we have no intention, in the use of such terms and expressions, of excluding any equivalents of the features shown and described or portions thereof, but we recognize that various modifications are possible within the scope of the invention claimed.
What is claimed is:
1. A pressure-sensitive copying material comprising a web having on at least a portion of a side thereof a coating having a melting point of between about 130 and 350 F., and consisting of a hydrophobic thermopla tic film-forming material, said film-forming material, having uniformly dispersed therein microscopic discrete non-viscous liquid droplets of a marking liquid which is substantially insoluble in said hydrophobic thermoplastic film-forming material, said coating when subjected to writing pressure, being rupturable thereby permitting the microscopic discrete liquid droplets to exude and produce a mark on an adjacent sheet.
2. A pressure-sensitive copying material as defined by claim 1 in which the marking liquid has a viscosity of less than about 50,000 centipoises at 70 F.
3. A pressure-sensitive copying material as defined by claim 1 in which the marking liquid has a viscosity of between about 30 and 30,000 centi oises at 70 F.
4. A pressure-sensitive copying material as defined by claim 1 in which the marking liquid comprises between about 20% and 60% of the weight of the coating.
5. A pressure-sensitive copying material comprising a web having on at least a portion of a side thereof a coating having a melting point of between about 130 and 350 F., said coating having a continuous phase of a hydrophobic thermoplastic film-forming material, said film-forming material which comprises between about 40% and 80% of the coating, and having a discontinuous phase comprising microscopic discrete non-viscous liquid droplets of a marking fluid substantially uniformly dispersed throughout the continuous phase.
6. A pressure-sensitive copying material comprising a web having on at least a portion of a side thereof a coating having a melting point of between about 130 and 350 F., and comprising a continuous phase of a rupturable hydrophobic thermoplastic film-forming material consisting of a polymer selected from the class consisting of natural hydrocarbon and coumarone-indene resins, a compatible waxy material and a hydrocarbon-soluble protective colloid and a discontinuous phase comprising microscopic discrete liquid droplets of a non-viscous marking fluid substantially uniformly dispersed throughout the continuous phase.
7. A pressure-sensitive copying material as defined by claim 6 wherein the polymer material comprises between about 25 and 80% by weight of the continuous phase, the compatible waxy material between about 10 and 75% by weight of the continuous phase, and the protective colloid between about 1 and 10% by weight of the continuous phase.
8. A stable hot-melt emulsion comprising a continuous phase of a hydrophobic thermoplastic film-forming composition being substantially a rigid solid at room tempera ture and having a melting point of between about 130 and 350 13., having dispersed therein microscopic discrete liquid droplets of a non-viscous marking fluid.
9. A stable hot-melt emulsion as defined by claim 8 in which the marking fluid has a viscosity of less than about 50,000 centipoises at 70 F.
10. A stable hot-melt emulsion as defined by claim 8 in which the marking fluid has a viscosity of between about 30 and 30,000 centipoises at 70 F.
11. A stable hot-melt emulsion as defined by claim 8 in which the liquid component of the marking fluid comprises between about 20 and 60% by weight of the total emulsion.
12. A stable hot-melt emulsion as defined by claim 8 in which the continuous phase contains at least one waxy material.
13. A stable hot-melt emulsion as defined by claim 8 in which the continuous phase comprises a polymeric resin selected from the class consisting of natural hydrocarbon and coumarone-indene resins having a melting point at a temperature of between about 130 and 350 F.
14. A stable hot-melt emulsion as defined by claim 12 in which the continuous phase comprises at least one WaXy and at least one thermoplastic polymeric material.
,15. A stable hot-melt emulsion as defined by claim 8 in which the continuous phase contains a protective colloid.
16. A stable hot-melt emulsion comprising a continuous phase having a melting point of between about 130 and 350 F., comprising about 25 to of a polymeric hydrophobic thermoplastic film-forming material selected from the class consisting of natural hydrocarbon and coumarone-indene resins, about 10 to 75% of a compatible waxy material and from 1 to 10% of a cyclized rubber resin and a discontinuous phase comprising microscopic discrete liquid droplets of a non-viscous marking fluid substantially uniformly dispersed throughout the continuous phase.
17. A process for producing a pressure-sensitive copying material comprising a web having on at least a portion of a side thereof a coating having a melting point of between about and 350 F., comprising a continuous phase of a hydrophobic thermoplastic film-forming material having dispersed therein microscopic discrete nonviscous liquid droplets of a marking fluid substantially uniformly dispersed throughout, said coating, when sub jected to writing pressure being rupturable, thereby permitting the microscopic discrete liquid droplets to exude and produce a mark on an adjacent sheet, which process comprises applying the molten coating to a sheet and permitting it to cool.
18. A process for producing a pressure-sensitive copying sheet as defined by claim 17 in which the marking fluid has a viscosity of less than about 50,000 centipoises at 70 F.
19. A process for producing a pressure-sensitive copying sheet as defined by claim 17 in which the marking fluid has a viscosity of between about 30 and 30,000 centipoises at 70 F.
20. A process for producing a pressure sensitive copying sheet as defined by claim 17 in which the continuous phase contains a waxy material.
21. A process for producing a pressure-sensitive copying sheet as defined by claim 17 in which the continuous phase contains a hydrocarbon-so1uble protective colloid.
References tilted in the file of this patent UNITED STATES PATENTS 2,413,432 Carson Dec. 31, 1946 2,663,656 Miller et al Dec. 22, 1953 2,710,263 Clark et al. June 7, 1955 2,711,375 Sandberg June 21, 1955 2,732,795 Brandt et al. Jan. 31, 1956 2,755,202 Balon et al. luly 17, 1956 2,820,717 Newman et a1 Ian. 21, 1958 3,016,308 Macaulay Jan. 9, 1962 3,020,170 Macaulay Feb. 6, 1962
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2413432 *||Jul 28, 1943||Dec 31, 1946||Wingfoot Corp||Rubber derivative products|
|US2663656 *||May 15, 1952||Dec 22, 1953||Minnesota Mining & Mfg||Heat-sensitive copying paper|
|US2710263 *||Feb 2, 1951||Jun 7, 1955||Minnesota Mining & Mfg||Heat-sensitive copying-paper|
|US2711375 *||Feb 19, 1954||Jun 21, 1955||Ncr Co||Pressure sensitive manifold sheet|
|US2732795 *||Dec 11, 1952||Jan 31, 1956||Stencil sheet assesfblx and cushion|
|US2755202 *||Sep 17, 1954||Jul 17, 1956||Du Pont||Stabilized coloring compositions and methods of making and using same|
|US2820717 *||Aug 17, 1953||Jan 21, 1958||Columbia Ribbon Carbon Mfg||Manifold sheet and composition therefor|
|US3016308 *||Aug 6, 1957||Jan 9, 1962||Moore Business Forms Inc||Recording paper coated with microscopic capsules of coloring material, capsules and method of making|
|US3020170 *||Oct 12, 1960||Feb 6, 1962||Moore Business Forms Inc||Transfer sheet and composition therefor|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3303046 *||Dec 30, 1963||Feb 7, 1967||Ibm||Method for making liquid-filled porous plastics and products|
|US3342622 *||Aug 10, 1964||Sep 19, 1967||Gestetner Ltd||Typewriter ribbon impregnated with ink comprising heat-polymerizable ester monomer|
|US3628979 *||Jun 20, 1968||Dec 21, 1971||Columbia Ribbon & Carbon||Transfer elements and method of making same|
|US3977992 *||Nov 8, 1971||Aug 31, 1976||Minnesota Mining And Manufacturing Company||Controlled release capsules|
|US3985840 *||Dec 20, 1973||Oct 12, 1976||Minnesota Mining And Manufacturing Company||Method of introducing microporosity into membranes and making capsules having microporous capsule walls|
|US4002458 *||Jul 30, 1975||Jan 11, 1977||Minnesota Mining And Manufacturing Company||Controlled release capsules|
|US4063754 *||May 7, 1976||Dec 20, 1977||The Mead Corporation||Process for the production of pressure sensitive carbonless record sheets using novel hot melt systems and products thereof|
|US4137343 *||Aug 29, 1977||Jan 30, 1979||The Mead Corporation||Process for producing pressure-sensitive carbonless transfer sheets|
|US4139218 *||Aug 29, 1977||Feb 13, 1979||The Mead Corporation||Process for producing pressure-sensitive carbonless manifolds|
|US4139392 *||Aug 29, 1977||Feb 13, 1979||The Mead Corporation||Chromogenic hot melt coating compositions|
|US4143890 *||Dec 6, 1976||Mar 13, 1979||The Mead Corporation||Pressure-sensitive carbonless transfer sheets using hot melt systems|
|US4171981 *||Apr 29, 1977||Oct 23, 1979||The Mead Corporation||Process for the production of hot melt coating compositions containing microcapsules|
|US4201404 *||May 17, 1978||May 6, 1980||Minnesota Mining And Manufacturing Company||Pressure-sensitive marking materials|
|US4208460 *||Nov 21, 1977||Jun 17, 1980||Blockfabrik Lichtensteig, AG||Process for producing paper having a coating of pressure-sensitive transfer copying material|
|US4235458 *||Jan 8, 1979||Nov 25, 1980||The Mead Corporation||Process for the production of hot melt coating compositions containing microcapsules|
|US4238549 *||Nov 27, 1978||Dec 9, 1980||Columbia Ribbon And Carbon Mfg. Co., Inc.||Transfer elements|
|US4327127 *||Jun 16, 1980||Apr 27, 1982||Columbia Ribbon & Carbon Mfg. Co., Inc.||Process for making transfer elements|
|US4336067 *||Mar 27, 1980||Jun 22, 1982||The Mead Corporation||Hot melt chromogenic coating composition|
|US4339143 *||Dec 18, 1979||Jul 13, 1982||Mishima Paper Co., Ltd.||Pressure-sensitive recording material|
|US4371634 *||Nov 16, 1981||Feb 1, 1983||Basf Aktiengesellschaft||Microcapsule-containing wax composition|
|US4372581 *||Oct 20, 1980||Feb 8, 1983||Hermann Schumacher||Pressure sensitive copying material|
|US4675236 *||Oct 30, 1985||Jun 23, 1987||Ohkawara Kokohki Co., Ltd.||Mono-core type microcapsules and process for producing them|
|US4693321 *||Nov 18, 1985||Sep 15, 1987||Conoco Inc.||Method using encapsulated flow improvers to reduce turbulence|
|US4729792 *||May 22, 1986||Mar 8, 1988||The Standard Register Company||Microcapsules, printing inks and their production|
|US4732810 *||Dec 23, 1985||Mar 22, 1988||Pilot Ink Co., Ltd.||Reversible temperature-indicating composition|
|US4889877 *||Jan 7, 1988||Dec 26, 1989||The Standard Register Company||High solids CB printing ink|
|US4898780 *||Jan 7, 1988||Feb 6, 1990||The Standard Register Company||Production of microcapsules|
|US4935260 *||Sep 19, 1988||Jun 19, 1990||Shlenker Robin R T||Covering such as a suit, glove, condum or sheath forming a chemical barrier against harmful agents and methods of making the same|
|US4940738 *||Aug 11, 1989||Jul 10, 1990||The Standard Register Company||High solids CB printing ink containing a protective colloid blend|
|US4940739 *||Dec 27, 1988||Jul 10, 1990||The Standard Register Company||Process for making a high solids CB printing ink|
|US5549924 *||Aug 15, 1994||Aug 27, 1996||Robin Renee Thill Shlenker||Method of forming a membrane, especially a latex or polymer membrane, including a deactivating barrier and indicating layer|
|US5679399 *||Jun 7, 1995||Oct 21, 1997||Bio Barrier, Inc.||Method of forming a membrane, especially a latex or polymer membrane, including multiple discrete layers|
|US5965276 *||Aug 13, 1997||Oct 12, 1999||Bio Barrier, Inc.||Method of forming a membrane especially a latex or polymer membrane including multiple discrete layers|
|DE2818976A1 *||Apr 28, 1978||Nov 2, 1978||Mead Corp||Verfahren zur herstellung einer heissen, geschmolzenen, mikrokapseln enthaltenden beschichtungsmasse|
|DE2820600A1 *||May 11, 1978||Dec 21, 1978||Mead Corp||Verfahren zur herstellung von mikrokapsel-beschichtungskompositionen mit pigmentartikeln und daraus hergestellten kompositionen|
|WO1980001263A1 *||Dec 18, 1979||Jun 26, 1980||Mishima Paper Co Ltd||Pressure-sensitive recording material|
|U.S. Classification||503/208, 503/214, 428/914, 427/146, 524/377, 524/526, 524/517|
|Cooperative Classification||Y10S428/914, B41M5/10|