GB2327129A - Heat sensitive stencils - Google Patents
Heat sensitive stencils Download PDFInfo
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- GB2327129A GB2327129A GB9814940A GB9814940A GB2327129A GB 2327129 A GB2327129 A GB 2327129A GB 9814940 A GB9814940 A GB 9814940A GB 9814940 A GB9814940 A GB 9814940A GB 2327129 A GB2327129 A GB 2327129A
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- film
- support
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
- B41C1/00—Forme preparation
- B41C1/14—Forme preparation for stencil-printing or silk-screen printing
- B41C1/144—Forme preparation for stencil-printing or silk-screen printing by perforation using a thermal head
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N1/00—Printing plates or foils; Materials therefor
- B41N1/24—Stencils; Stencil materials; Carriers therefor
- B41N1/245—Stencils; Stencil materials; Carriers therefor characterised by the thermo-perforable polymeric film heat absorbing means or release coating therefor
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Printing Plates And Materials Therefor (AREA)
Abstract
A heat sensitive stencil comprises a porous support (10) and a thermoplastic resin film (20) laminated on the support. The surface of the resin film opposite to that contracting the support has a surface smoothness of at least 10,000 seconds. The heat sensitive stencil may be made by bonding the resin film to the porous support with an adhesive, while maintaining both the support and film under a specific tension. Another process of fabricating a heat sensitive stencil is disclosed, and which involves applying a coating composition containing a resin and first and second solvents having a specific solubility and specific evaporation rates, to one surface of the thermoplastic resin film, followed by drying the applied composition to form a porous support. In an alternative process of fabricating a heat sensitive stencil, a resin dissolved in a solvent, is applied to one surface of the thermoplastic resin film, to form a wet resin coating over this surface, followed by spraying vapours or fine droplets of a second solvent overthe wet coating, the second solvent being incapable of dissolving the resin, followed by drying the resin coating to form a porous support.
Description
TITLE OF THE INVENTION
Heat-Sensitive Stencil, Process of Fabricating Same
and Method of Producing Printing Master Using Same
BACKGROUND OF THE INVENTION
This invention relates to a heat-sensitive stencil, to a process of fabricating same and a method of producing a printing master using same.
One known heat-sensitive stencil is composed of an ink-permeable thin paper serving as an ink support and a thermoplastic resin film bonded with an adhesive to the support. The stencil is heated imagewise by, for example, a thermal head to perforate the heated portions of the thermoplastic resin film, thereby obtaining a printing master for reproducing images by mimeographic printing.
An overcoat layer is generally provided over a surface of the thermoplastic resin film to prevent the sticking of the film with the thermal head.
The known heat-sensitive stencil has a problem, because the heated portions are not completely perforated.
The portion of the stencil which remains unperforated results in a white spot in reproduced images obtained therefrom. This problem can be overcome by increasing thermal energy for the perforation. However, an increase of the thermal energy causes an increase of the master producing time as well as a shortened service life of the heating means.
A method has been proposed to increase the heat sensitivity of the stencil by reducing the thickness of the thermoplastic resin film, by using a low softening resin as the film or by using a resin having a great thermal shrinkage as the film. This method, however, requires an increased cost and, further, causes deterioration of physical properties of the stencil.
An attempt has also been made to increase the smoothness of the surface of the film with a view toward reducing perforation failure. JP-A-H5-212983 discloses a method of producing a smooth surface stencil by controlling a tension between a thermoplastic resin film and a support during lamination thereof. JP-A-H8-67081 discloses a method of producing a smooth surface stencil by heat-bonding a thermoplastic resin film and a support without using an adhesive. These methods give a smoothness of at most 5,000 seconds, even when the film originally has a surface smoothness of more than 10,000 seconds.
SUMMARY OF THE INVENTION
It has now been found that a surface smoothness of a stencil of 5,000 seconds is insufficient to prevent perforation failure, especially when the stencil is perforated by a thermal head with a small heat energy of not greater than 0.05 mJ/dot. The formation of printing masters with such a small energy is strongly desired in the field. It has also been found that a surface smoothness of at least 10,000 seconds, preferably 15,000 seconds, is required to obtain satisfactory perforation with a thermal energy of a thermal head of not greater than 0.05 mJ/dot.
It is an object of the present invention to provide a heat-sensitive stencil which can be thermally perforated uniformly with a thermal head using a small heat energy.
Another object of the present invention is to provide an economical process for the fabrication of a heat-sensitive stencil of the above-mentioned type.
It is a further object of the present invention to provide a method of forming a high quality printing master even using a small heat energy.
In accomplishing the foregoing objects, there is provided in accordance with one aspect of the present invention a heat-sensitive stencil comprising a porous support, and a thermoplastic resin film laminated on said support and having a surface smoothness of at least 10,000 seconds.
In another aspect, the present invention provides a process of fabricating a heat-sensitive stencil, comprising bonding a thermoplastic resin film having opposing first and second surfaces, said second surface having a surface smoothness of at least 10,000 seconds, to a porous support with an adhesive having a viscosity of at least 1,000 mPa s and containing a non-volatile matter such that said first surface faces on said support, said bonding being performed while maintaining each of said support and said film under a tension of at least 1 kgf/m in the same direction and while maintaining a ratio of the tension of said support in said direction to the tension of said film in said direction in the range of 1-4, said adhesive being used in such an amount that said nonvolatile matter is present between said film and said support in an amount of 0.05-1.0 g of per m2 of said film, so that said second surface of said film laminated on said support has a surface smoothness of at least 10,000 seconds.
In a further aspect, the present invention provides a process of fabricating a heat-sensitive stencil, comprising the steps of:
applying a coating composition to one of the both surfaces of a thermoplastic resin film, said composition containing a resin, a first solvent capable of dissolving said resin, and a second solvent substantially incapable of dissolving said resin and having an evaporation rate lower than that of said first solvent, said film having the other surface with a smoothness of at least 10,000 seconds; and
drying said applied composition to form a porous support on said one surface of said film.
The present invention also prcvides a process of fabricating a heat-sensitive stencil, comprising the steps of:
applying a solution of a resin in a first solvent to one of the both surfaces of a thermoplastic resin film to form a wet resin coating over said one surface, said film having the other surface with a smoothness of at least 10,000 seconds;
spraying vapors or fine droplets of a second solvent substantially incapable of dissolving said resin over said wet resin coating so that said second solvent is taken into said wet resin coating to cause a portion of said resin to precipitate; and
then drying said resin coating to form a porous support on said one surface of said film.
The present invention further provides a method of producing a printing master, comprising heating a heatsensitive stencil imagewise by a thermal head with heating energy of not greater than 0.05 mJ/dot, said stencil comprising a porous support, and a thermoplastic resin film laminated on said support and aving a surface smoothness of at least 10,000 second.
BRIEF DESCRIPTION OF THE DRAWINGS
Other objects, features and advantages of the present invention will become apparent from the detailed description of the preferred embod'-ents of the invention which follows, when considered in light of the accompanying drawings, in which:
Figs. 1-4 are sectional views schematically illustrating various embodiments of heat-sensitive stencils according to the present invention.
DETAILED DESCRIPTION OF THE PREFERRED
EMBODIMENTS OF THE INVENTION
Referring Figs. 1-4, designated generally as 101, 201, 301 and 401 are heat-sensitive stencils according to the present invention. The reference numeral 10 designates a porous support, 20 a thermoplastic resin film, 30 an overcoat layer and 40 a backcoat layer. The overcoat layer 30 and the backcoat layer 40 are optionally provided as desired.
The thermoplastic resin film 20 may be made of any conventionally employed resin such as a polyester resin.
The thickness of the film 20 is suitably determined with the consideration of easiness in handling during preparation of the stencil and desirable heat sensitivity during the perforation with a thermal head and is generally 0.5-10 pm, preferably 1.0-5.0 pm. It is important that the thermoplastic resin film 20 should have a surface smoothness of at least 10,000 seconds, preferably at least 15,000 seconds in order to achieve the objects of the present invention.
The term "smoothness" herein is as measured in accordance with Oken Smoothness Test Method described in
JAPAN TAPPI No. 5-B. An Oken-type smoothness measuring device (KY-55 manufactured by Kumagaya Riki Kogyo K. K.) is suitably used for this method. Before measurement of smoothness, samples are allowed to stand for 24 hours in an atmosphere maintained at a temperature of 200C and a relative humidity of 65 %. Measurement is made on arbitrary three areas of a sample and an average of the three measured values represents the smoothness of the film.
The overcoat layer 30 is provided over the thermoplastic resin film 20 and is brought into sliding contact with a thermal head in producing a printing master rom the stencil 201 or 401. The overcoat layer 30 functions to prevent the sticking between the thermal head and the stencil, so that the thermal head can smoothly run or slide on the stencil. The overcoat layer 30 can also serves to function as an antistatic layer. It is important that the overcoat layer 30 should have a surface smoothness of at least 10,000 seconds, preferably at least 15,000 seconds in order to achieve the objects of the present invention. The overcoat layer 30 may be a resin layer optionally containing one or more additives such as a metal salt of a fatty acid, a phosphate surfactant, a lubricant such as a silicone oil, or a fluorocarbon containing a perfluoroalkyl group, a lubricant and an antistatic agent. Alternatively, the overcoat layer 30 may be an oil layer or a layer of an inorganic or organic fine powder of, for example, a lubricant, an antistatic agent or a releasing agent. Since the overcoat layer 30 is formed on the thermoplastic resin film 20, the surface smoothness of the overcoat layer 30 generally depends upon that of the film 20.
The backcoat layer 40 is provided on the porous support 10 to improve the rigidity of the stencil, running or sliding property of the stencil on a master forming device and a printing device and to prevent the curling, static charging and blocking of the stencil. The backcoat layer 40 is desirably more porous than the porous support 10.
The porous support 10 may be a thin paper having a thickness of generally 5-70 urn, preferably 10-55 pm, and a basis weight of generally 5-15 g/m2 and formed of natural and/or synthetic fibers. The natural fibers may be, for example, those of wood, cotton, kozo (Broussonetia kazinoki), mitsumata (Edgeworthia papyrifera), ganpi (Wikstroemia sikokiana Fr, et Sav.), a flax plant, Manila hemp, straw and bagasse. The synthetic fibers may be, for example, polyester fibers, vinylon fibers, acrylic fibers, polyethylene fibers, polypropylene fibers, polyamide fibers and rayon fibers. Alternatively, the porous support 10 may be a porous resin layer.
When the porous support 10 is a thin paper, the stencil is prepared by the following process:
The thermoplastic resin film 20 and the porous support 10 are bonded to each other with an adhesive having a viscosity of at least 1,000 mPa s and containing a non-volatile matter. The film 20 has opposing first and second surfaces wherein at least the second surface has a surface smoothness of at least 10,000 seconds. The bonding is carried out such that the first surface of the film 20 faces on the support 10. During the bonding, each of the support 10 and the film 20 is subjected to a tension of at least 1 kgf/m in the same direction, while maintaining a ratio of the tension of the support 10 in that direction to the tension of the film 20 in that direction in the range of 1:1 to 4:1. The adhesive is used in such an amount that the non-volatile matter is present between the film 20 and the support 10 in an amount of 0.05-1.0 g of per m2 of the film 20 (namely per m2 of the bonding area). By bonding the film 20 and the support 10 in the above condition, the second surface of the film 20 laminated on the support 10 has a surface smoothness at least 10,000 seconds.
When the tension ratio is smaller than 1:1, the laminate is apt to curl. Too high a tension ratio in excess of 4:1 causes shrinkage of the film 20 so that the smoothness is significantly lowered. It is also important that a tension of at least 1 kgf/m should be applied to the film 20 in order to maintain the surface smoothness thereof.
The adhesive is a solvent solution of a resin such as an acrylic resin, a vinyl resin, an ethylene resin, an amide resin, an urethane resin or a cellulose resin. The viscosity of the adhesive should be at least 1,000 mPa s at the time the film 20 has just been brought into contact with the support 10 through the adhesive. The viscosity can be determined by previous experiments. It is preferred that the adhesive be applied to the film 20 rather than to the support 10 for reasons of obtaining a better smoothness of the film. The amount of the adhesive (solid matter) also has been found to have an influence upon the smoothness and should fall within the abovedescribed range.
When the porous support 10 is a porous resin layer, the stencil may be prepared by the following two processes.
In one process, a resin for forming the porous resin layer is first dissolved, completely or partly, in a mixed solvent including a first solvent (good solvent) capable of dissolving the resin and a second solvent (poor solvent) substantially incapable of dissolving the resin and having a lower evaporation rate than the first solvent, thereby te obtain a coating liquid in the form of a solution or a dispersion. Preferably the second solvent has a boiling point which is higher by 10-400C than that of the first solvent and which is preferably 1500C or less.
The concentration of the resin in the mixed solvent solution is generally 2-50 % by weight, preferably 5-30 % by weight. The weight ratio of the first solvent to the second so vent, which has an influence upon the pore structure of the porous resin layer, is generally 40:60 to 95:5.
The thus obtained coating liquid is then applied over a surface of a thermoplastic resin film to form a wet resin coating. The application of the coating liquid may be carried out by any desired coating method such as blade coating, transfer roll coating, wire bar coating, reverse roll coating or gravure coating. In this case, it is preferred that the coating liquid immediately before being applied be heated at a temperature higher than that of the atmosphere at which the coating step is performed and which is generally room temperature. Thus, when the coating is performed with a die coater, the die from which the solution is applied to the thermoplastic resin film may be surrounded by a heating jacket to which a heating medium is fed. It is also preferred that coating liquid immediately after being applied to the thermoplastic resin film be cooled before the next drying step to a temperature lower by 2-300C, preferably 5-200C, than that of the coating liquid immediately before being applied.
The wet resin coating is then heated at a temperature below the boiling point of the second solvent but sufficient to vaporize part of the first solvent so that a portion of the resin precipitates. Subsequently, the coating is further heated preferably at 800C or less until the coating is completely dried. During the course of the vaporization of the solvents, there are formed a multiplicity of pores.
Examples of suitable poor and good solvents are shcwn in Table 1 below. As shown, good and poor solvents vary with the resin to be dissolved.
Table 1
Resin PVC*1 VCA*2 PB+3 PS*4 ANS*5 ALS*6 Solvent(b.p. C) Methanol(64.5) poor poor poor poor poor poor
Ethanol(78.3) poor poor poor - - poor
Ethyl acetate(77.1) - good poor good good Acetone (56.1) good good poor good good good
Methyl ethyl
ketone(79.6) good good poor good good good
Diethyl ether(34.5) poor - - poor poor poor
Tetrahydrofuran
(65-67) good good good good
Hexane(68.7) poor poor good poor poor
Heptane(98.4) poor poor poor poor poor poor Benzene(80.1) - poor good good good good Toluene(lI0.6) - good good good good good Xylene(139.1) - good good good good good Chloroform(61.2) - good good good good good
Carbon tetra
chloride(76.7) - good good good - Water(100.0) poor poor poor poor poor poor
*1 PVC: poly(vinyl chloride)
*2 VCA: vinyl chloride-vinyl acetate copolymer *3 PB: polybutylene *4 PS: polystyrene *5 ANS: acrylonitrile-styrene copolymer
*6 ABS: acrylonitrile-butadiene-styrene copolymer *7 MAR: methacrylic acid resin *8 PVA: poly(vinyl acetate)
*9 PC: polycarbonate
*10 AC: acetylcellulose resin
*11 AR: acrylate resin *12 VB: polyvinyl-butyral
Table 1 (continued)
Resin MAR+7 PVA*8 PC+9 AT* 10 At*11 VB*12 Solvent(b.p.oC1 Methanol(64.5) - good poor - poor good
Ethanol(78.3) - poor poor - poor good
Ethyl
acetate(77.1) good good poor good good good Acetone(56.1) good good poor good good good
Methyl ethyl
ketone(79.6) good good poor good - good
Diethyl
ether(34.5) - poor - - - poor
Tetrahydrofuran
(65-67) good - good good - good
Hexane(68.7) poor poor poor poor poor poor
Heptane(98.4) poor poor poor poor poor poor Benzene(80.1) good good good - good poor
Toluene(110.6) good good good poor good poor
Xylene(139.1) good good good poor good
Chloroform(61.2) good good good good good
Carbon tetra
chloride(76.7) - - good poor -
Water(100.0) poor poor poor poor poor poor
Any resin may be used for the formation of the porous layer. Illustrative of suitable resins of the porous layer are a vinyl resin such as poly(vinyl acetate), poly(vinyl butyral), poly(vinyl acetal), vinyl chloridevinyl acetate copolymer, vinyl chloride-vinylidene chloride copolymer or styrene-acrylonitrile copolymer; a polyamide such as nylon; polybutylene; polyphenylene oxide; (meth)acrylic ester; polycarbonate; or a cellulose derivative such as acetylcellulose, acetylbutylcellulose or acetylpropylcellulose. These resins may be used singly or in combination of two or more. It is preferred that the porous resin layer contain a resin capable of softening at a temperature at which the perforation by a thermal head is carried out, generally at a temperature of 150 C or less, for reasons of facilitating the perforation of the thermoplastic resin film.
The porous resin layer can contain one or more additives such as a filler, an antistatic agent, a stickpreventing agent, a surfactant, an antiseptic agent and an antifoaming agent. Addition of a filler to the porous resin layer is desirable to control the strength, stiffness and the size of pores thereof. Use of a filler in the form of needles or plates is particularly preferred.
Illustrative of suitable fillers are needle-like natural mineral fillers such as magnesium silicate, sepiolite, potassium titanate, wollastonite, zonolite and gypsum fiber; needle-like synthetic mineral fillers such as nonoxide-type needle whiskers, oxide whiskers and mixed oxide whiskers; platy fillers such as mica, glass flakes and talc; pigments such as poly(vinyl chloride) particles, poly(vinyl acetate) particles, polymethyl acrylate particles, zinc oxide, titania, calcium carbonate and microcapsules (e.g. Matsumoto Microsphere); and natural or synthetic fibers such as carbon fiber, polyester fiber, glass fiber, vinylon fiber, nylon fiber and acrylic fiber.
The filler is generally used in an amount of 0.5-200 %, preferably 8-20 % based on the weight of the resin of the porous resin layer.
In the second process, a solution of a resin for the porous resin layer in a first solvent is prepared. The solution is applied over a surface of a thermoplastic resin film to form a wet resin coating over the surface.
Then, vapors or fine droplets of a second solvent substantially incapable of dissolving the resin are sprayed over the wet resin coating so that the second solvent is taken into the wet resin coating to cause a portion of the resin to precipitate. Thereafter, the resin coating is heated to dryness. The first and second solvents, the resin and optional additives used for the formation of the porous layer in the second method are similar to those described above in connection with the first method. In the second method, the size and number of pores may be controlled by the amount and particle size of the droplets of the second solvent. It is preferred that the thermoplastic resin film be previously applied with a spray of the second solvent before being applied with the solvent solution of the resin, since the contact area between the resulting porous resin layer and the thermoplastic resin film is decreased and, therefore, the stencil can be more easily perforated by a thermal head.
If desired, the above first and second methods may be combined for the fabrication of the stencil according to the present invention.
The heat-sensitive stencil thus formed by the above first or second methods has a porous resin layer serving as an ink support and formed on a thermoplastic resin film.
The stencil is adapted show an air permeability in the range of 3.0 cm3/cm2 sec to 200 cm3/cm2 sec, preferably 10 cm3/cm2 sec to 80 cm3/cm2 sec, in a portion thereof when the thermoplastic resin film of that portion is perforated to form perforations providing an open ratio SO/SP of at least 0.2, wherein SO represents a total area of the perforations and Sp represents the area of the portion.
The air permeability may be measured in the following manner. A square solid pattern (black pattern) with a size of 10 x 10 cm is read by a printer (PRIPORT VT 3820 manufactured by Ricoh Company, Ltd.) and a sample stencil is perforated with a thermal head in accordance with the read out pattern to form a printing master. The perforation operations are performed for five similar samples so that five printing masters having open ratios SO/SP of about 0.2, 0.35, 0.50, 0.65 and 0.80 are obtained.
The open ratio of a master may be measured by making a photomicrograph (magnification: 100) thereof. The photomicrograph is then magnification-copied (magnifying ratio: 200) using a copying machine (IMAGIO MF530 manufactured by Ricoh Company, Ltd.). Perforations shown in the copy are marked on an OHP film and then read by a scanner (300 DPI, 256 gradient). This is binarized with an image retouch software Adobe Photoshop 2.SJ. The open ratio of the perforations is measured using an image analysis software NIH IMAGE. The perforated portion of each of the printing masters is measured for the air permeability thereof by any conventional method. When at least one of the five masters has an air permeability in the range of 1.0 cm3/cm2 sec to 157 cm3/cm2sec, the stencil is regarded as falling within the scope of the present invention.
The porous resin layer preferably has an average pore diameter of 2-50 urn, more preferably 5-30 Wm, for reasons of proper ink permeability. The porous resin layer preferably has a thickness of 5-100 um, more preferably 6-50 from, for reasons of proper stiffness of the stencil and proper ink transference. The density of the porous resin layer is preferably 0.01-1 g/cm3, more preferably 0.1-0.7 g/cm3, for reasons of proper stiffness and mechanical strengths. If desired, an adhesive layer may be interposed between the porous resin layer and the thermoplastic resin film.
The following examples will further illustrate the present invention. Parts and percentages are by weight.
Example 1
An urethane resin adhesive containing substantially no volatile matters was applied to one surface of a porous sheet support, made of a polyester fiber (0.2 denier: 10 %, 0.5 denier: 40 %, 1.2 denier: 50 %) and having a base weight of 10 g/m2, in an amount of 0.5 g per m2 of the surface. The adhesive when applied to the porous support had a temperature of 900C and a viscosity of 1,300 aPa (measured by B-type viscometer). After the temperature of the adhesive applied to the surface of the support had been lowered to about 500C, a biaxially oriented polyester film having a thickness of about 1.S urn and a surface smoothness of more than 30,000 seconds was applied thereon, while maintaining the film and the support under tensions of 2 kgf/m and 5 kgf/m, respectively, in the same direction. The assembly was then allowed to be cooled to room temperature while maintaining the tensions applied to the film and the support unchanged. A liquid containing a silicone resin and a cationic antistatic agent was applied on the back side of the polyester film opposite the support and dried to form a stick preventing layer (overcoat layer), thereby obtaining a heat-sensitive stencil according to the present invention having a structure shown in Fig. 2.
Comparative Example 1
Example 1 was repeated in the same manner as described except that the amount of adhesive was increased to 1.5 g/m2.
Comparative Example 2
Example 1 was repeated in the same manner as described except that the adhesive when applied to the porous support had a temperature of 1200C and a viscosity of 600 mPa s.
Comparative Example 3
Example 1 was repeated in the same manner as described except that the tension applied to the support was increased to 10 kgf/m.
Example 2
Poly(vinyl butyral) 4 parts
Methanol 33.6 parts
Water 2.8 parts
The above composition was stirred to dissolve the resin in the mixed solvent and allowed to quiescently stand to remove foams. The solution was then uniformly applied to a biaxially stretched polyester film (thickness: 1.5 um, surface smoothness: more than 30,000 seconds) with a wire bar at a temperature of 200C and a relative humidity of 60 %, thereby to form a wet coating having a deposition amount of 7.0 g/cm2 (on dry basis).
This was allowed to stand as such for 15 seconds and then placed in a drying chamber at 500C for 1 minute to dry the coating and to a porous layer. A liquid containing a silicone resin and a cationic antistatic agent was applied on the back side of the polyester film opposite the porous layer and dried to form a stick preventing layer (overcoat layer), thereby obtaining a heat-sensitive stencil according to the present invention having a structure shown in Fig. 2.
Example 3
Cellulose acetate butylate
(softening point: 1310C) 5 parts
Methyl ethyl ketone 85 parts
The above composition was stirred to dissolve the resin in the solvent and allowed to quiescently stand to remove foams. The solution was then uniformly applied to a biaxially stretched polyester film (thickness: 1.5 Wm, surface smoothness: more than 30,000 seconds) with a wire bar at a temperature of 300C and a relative humidity of 90 %, thereby to form a wet coating having a deposition amount of 7.0 g/cm (on dry basis). Fine droplets of water were sprayed for 15 seconds from Humidiffer UV-107D (manufactured by Hitachi Inc.) over the surface of the wet coating placed at a distance 10 cm away from the
Humidiffer. This was allowed to stand as such for 1 minute and then placed in a drying chamber at 500C for 2 minutes to dry the coating. The dried coating was a porous layer. A liquid containing a silicone resin and a cationic antistatic agent was applied on the back side of the polyester film opposite the porous layer and dried to form a stick preventing layer (overcoat layer), thereby obtaining a heat-sensitive stencil according to the present invention having a structure shown in Fig. 2.
Each of the thus obtained heat-sensitive stencils was measured for surface smoothness, open ratio, air permeability, perforation efficiency and printed image quality. The surface smoothness, open ratio and air permeability were measured by the methods described previously. The perforation efficiency was measured by perforating a sample with a thermal head of 600 dots/in at an energy of 0.03 mJ/dot using PRIPORT VT 3820 (manufactured by Ricoh Company Ltd.) to form 10x10 dots.
The perforated sample was observed with a microscope (magnification: 110) and the dots actually perforated were counted. The perforation efficiency is expressed as a percentage of the number of the perforated dots based on 10x10 dots. Image quality was evaluated with naked eyes for prints (solid pattern image) obtained using sample stencil with respect to white spots and blurs. Evaluation was made by comparison with the image obtained using a commercial stencil (VT2 Master manufactured by Ricoh
Company Ltd.) and rated as follows: 5: much better, 4: slightly better, 3: comparable, 2: slightly inferior, 1: much inferior. The results are shown in Table 1.
Table 1
Example Smooth- Open Air Per- Perfora- Image ness ratio meability tion Effi- quality (sec) (%) (cm3/cm2-sec) ciency (%) Example 12,000 20 9 100 5 1 35 14 48 19 63 25 79 30 Compa- 4,700 20 9 92 2 native 35 13 Example 48 17 1 63 20 79 28 Compa- 6,400 20 8 95 3 rative 35 12 Example 48 16 2 63 21 79 29 Compa- 2,900 20 5 89 rative 35 11 Example 48 14 3 63 19 79 27 Example 22,000 20 4 100 5 2 35 9 48 12 63 16 79 24 Example 21,000 20 4 100 5 3 35 9 48 13 63 16 79 25 e invention may be embodied in other specific forms without departing from the spirit or essential cnaracteristics thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all the changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
The teachings of Japanese Patent Application =. H9200897, filed July 10, 1997 and entitled "Heat-Sensitive
Stencil Master, Process of Preparing Same and Method of
Preparing Printing Master", inclusive of the specification, claims and drawings, are hereby incorporated by reference herein.
Claims (8)
1. A heat-sensitive stencil comprising a porous support, and a thermoplastic resin film laminated on said support and having a surface smoothness of at least 10,000 seconds.
2. A heat-sensitive stencil as set forth in claim 1, wherein said film is laminated on said support with an adhesive layer interposed therebetween.
3. A heat-sensitive stencil as set forth in claim 1, further comprising an overcoat layer provided on said film and having a surface smoothness of at least 10,000 seconds.
4. A process of fabricating a heat-sensitive stencil, comprising bonding a thermoplastic resin film having opposing first and second surfaces, said second surface having a surface smoothness of at least 10,000 seconds, to a porous support with an adhesive having a viscosity of at least 1,000 mPa s and containing a non-volatile matter such that said first surface faces on said support, said bonding being performed while maintaining each of said support and said film under a tension of at least 1 kgf/m in the same direction and while maintaining a ratio of the tension of said support in said direction to the tension of said film in said direction in the range of 1-4, said adhesive being used in such an amount that said nonvolatile matter is present between said film and said support in an amount of 0.05-1.0 g of per m2 of said film, so that said second surface of said film laminated on said support has a surface smoothness of at least 10,000 seconds.
5. A process as set forth in claim 4, further comprising applying a coating liquid to said thermoplastic resin film, and drying said applied liquid to form an overcoat layer thereon.
6. A process of fabricating a heat-sensitive stencil, comprising the steps of:
applying a coating composition to one of the both surfaces of a thermoplastic resin film, said composition containing a resin, a first solvent capable of dissolving said resin, and a second solvent substantially incapable of dissolving said resin and having an evaporation rate lower than that of said first solvent, said film having the other surface with a smoothness of at least 10,000 seconds; and
drying said applied composition to form a porous support on said one surface of said film, so that said the other surface of said film laminated on said support has a surface smoothness of at least 10,000 seconds.
7. A process of fabricating a heat-sensitive stencil, comprising the steps of:
applying a solution of a resin in a first solvent to one of the both surfaces of a thermoplastic resin film to form a wet resin coating over said one surface, said film having the other surface with a smoothness of at least 10,000 seconds;
spraying vapors or fine droplets of a second solvent substantially incapable of dissolving said resin over said wet resin coating so that said second solvent is taken into said wet resin coating to cause a portion of said resin to precipitate; and
then drying said resin coating to form a porous support on said one surface of said film, so that said the other surface of said film laminated on said support has a surface smoothness of at least 10,000 seconds.
8. A method of producing a printing master, comprising heating a heat-sensitive stencil imagewise by a thermal head with a heating energy of not greater than 0.05 mJ/dot, said stencil comprising a porous support, and a thermoplastic resin film laminated on said support and having a surface smoothness of at least 10,000 seconds.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9200897 | 1997-07-10 | ||
JP19679998A JP3632056B2 (en) | 1997-07-10 | 1998-06-26 | Master for thermal stencil printing and its plate making method |
Publications (3)
Publication Number | Publication Date |
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GB9814940D0 GB9814940D0 (en) | 1998-09-09 |
GB2327129A true GB2327129A (en) | 1999-01-13 |
GB2327129B GB2327129B (en) | 2000-11-08 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB9814940A Expired - Lifetime GB2327129B (en) | 1997-07-10 | 1998-07-09 | Heat-sensitive stencil,process of fabricating same and method of producing printing master using same |
Country Status (1)
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GB (1) | GB2327129B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2350691A (en) * | 1999-05-31 | 2000-12-06 | Tohoku Riko Kk | Thermosensitive stencil |
EP1066979A2 (en) * | 1999-07-07 | 2001-01-10 | Riso Kagaku Corporation | High-sensitive stencil sheet and method for producing the same |
EP1090777A2 (en) * | 1999-10-08 | 2001-04-11 | Ricoh Company, Ltd | Heat-sensitive stencil and process of fabricating the same |
EP1293358A2 (en) * | 2001-09-18 | 2003-03-19 | Riso Kagaku Corporation | Source sheet for stencil printing, plate manufacturing method, and stencil printing method |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11739229B2 (en) * | 2020-05-27 | 2023-08-29 | Riso Kagaku Corporation | Treatment liquid for screen printing plate and method for treating screen printing plate |
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GB1404696A (en) * | 1973-08-01 | 1975-09-03 | Asahi Dow Ltd | Heat-sensitive copying method for preparing printing stencils |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2350691A (en) * | 1999-05-31 | 2000-12-06 | Tohoku Riko Kk | Thermosensitive stencil |
GB2350691B (en) * | 1999-05-31 | 2001-07-25 | Tohoku Riko Kk | Thermosensitive stencil production method thereof thermosensitive stencil printing master making apparatus and thermosensitive stencil printing apparatus |
US6393979B1 (en) | 1999-05-31 | 2002-05-28 | Ricoh Company, Ltd. | Thermosensitive stencil, production method thereof, thermosensitive stencil printing master making apparatus and thermosensitive stencil printing apparatus |
EP1066979A2 (en) * | 1999-07-07 | 2001-01-10 | Riso Kagaku Corporation | High-sensitive stencil sheet and method for producing the same |
EP1066979A3 (en) * | 1999-07-07 | 2001-04-11 | Riso Kagaku Corporation | High-sensitive stencil sheet and method for producing the same |
EP1090777A2 (en) * | 1999-10-08 | 2001-04-11 | Ricoh Company, Ltd | Heat-sensitive stencil and process of fabricating the same |
EP1090777A3 (en) * | 1999-10-08 | 2002-05-22 | Ricoh Company, Ltd | Heat-sensitive stencil and process of fabricating the same |
US6889605B1 (en) | 1999-10-08 | 2005-05-10 | Ricoh Company, Ltd. | Heat-sensitive stencil, process of fabricating same and printer using same |
EP1293358A2 (en) * | 2001-09-18 | 2003-03-19 | Riso Kagaku Corporation | Source sheet for stencil printing, plate manufacturing method, and stencil printing method |
EP1293358A3 (en) * | 2001-09-18 | 2003-08-13 | Riso Kagaku Corporation | Source sheet for stencil printing, plate manufacturing method, and stencil printing method |
US6841233B2 (en) | 2001-09-18 | 2005-01-11 | Riso Kagaku Corporation | Source sheet for stencil printing, plate manufacturing method, and stencil printing method |
Also Published As
Publication number | Publication date |
---|---|
GB2327129B (en) | 2000-11-08 |
GB9814940D0 (en) | 1998-09-09 |
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