EP0377935B1 - Höchst wärmeempfindlicher Mehrschichtfilm und Herstellungsverfahren für eine Schablone - Google Patents

Höchst wärmeempfindlicher Mehrschichtfilm und Herstellungsverfahren für eine Schablone Download PDF

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Publication number
EP0377935B1
EP0377935B1 EP19890307285 EP89307285A EP0377935B1 EP 0377935 B1 EP0377935 B1 EP 0377935B1 EP 19890307285 EP19890307285 EP 19890307285 EP 89307285 A EP89307285 A EP 89307285A EP 0377935 B1 EP0377935 B1 EP 0377935B1
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EP
European Patent Office
Prior art keywords
layer
peeling
functional layer
film
layers
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EP19890307285
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English (en)
French (fr)
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EP0377935A2 (de
EP0377935A3 (de
Inventor
Isao Yoshimura
Toshiaki Ohno
Hideo Hata
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Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
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Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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    • 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

Definitions

  • This invention relates to a novel high-sensitivity thermosensitive multilayer film and a method for the production of a stencil sheet using the film. More particularly, this invention relates to a high-sensitivity thermosensitive multilayer film suitable for use in the production of a stencil sheet for recording therein information on a given original by being perforated with the image or lettering of the information at a prescribed position by direct heating with the pulsating irradiation using a laser beam, particularly a semiconducting laser beam of low energy; a LED beam; indirect heating from heating a given original by flashing instantaneous irradiation using a flash lamp or a xynon-krypton lamp and transferring the heat to the film; or contact conduction of heat with a thermal head.
  • a known method comprises tightly superposing on the film surface of the stencil sheet an original having lettering or an image expressed thereon formed with ink or toner capable of absorbing a ray; causing the original to generate heat by means of an infrared ray or flash light from a xenon lamp; and conducting the heat to the film surface thereby melting the film causing the required perforation and consequently obtaining a suitable plate.
  • a known stencil sheet to be used in this method of plate making comprises a laminate produced by stretching a polyethylene terephthalate film in an independent form and to about 2 »m in thickness with an extremely expensive high-precision tenter and, at the same time, thoroughly heat-treating the film in the posterior part of the same tenter thereby crystallizing the resin of the film (to crystallinity of about 45% as determined by the density method) and subsequently superposing the resultant stretched film on a supporting member such as onion paper or sheet (in a meshed form) with the use of an adhesive agent.
  • this laminate possesses sufficient resistance to heat and exhibits highly satisfactory dimensional stability, it inevitably sustains scratches, wrinkles, warp, strain (uneven tention), and breakage because, during the aforementioned super-position of the film on the supporting member through the medium of the adhesive agent, the adhesion of the supporting member to the film occurs with surface irregularities of the supporting member persisting and manifesting themselves through the film surface to the extent that they jeopardize the microscopic smoothness of the film surface and disrupt the evenness of thickness of the film due to uneven application of the adhesive agent along the interface.
  • the superposition of one such polyethylene terephthalate film on the supporting member is carried out in a stretched state with meticulous care. In spite of the elaboration, it is difficult to obtain the laminate with fully satisfactory uniformity.
  • the plate for printing is made of a stencil sheet which has inferior quality due to the performance of the laminating method, it results in disadvantages such as the phenomenon of curling the separation of layers along the interface of adhesion, and heavy local deterioration of sensitivity or resolution.
  • high energy perforating means are used, this problem does not require a very serious consideration. The problem, however, dictates a very serious consideration when low energy perforating means are used.
  • Thermal heads provided with very small heating elements (10 to 16 dots/mm, for example) are utilized extensively in various types of printers, word processors, and facsimiles which are now tending toward digitization have been subjected to a special study aimed at miniaturization, improvement in operating speed, and economization of energy.
  • the stencil sheet to be used for the production of the plate is particularly required to exhibit high sensitivity and high resolution and possess a uniform quality.
  • the stencil sheet which is produced as described above is unsatisfactory in terms of the recovery of solvent and the speed of drying on account of the process of production and, moreover, is disadvantageous in inevitably losing locally the uniformity of thickness of the film and consequently having a restriction as to the lower limit of film thickness. Further, this method has no alternative but to use a film of low softening point because it is required to improve sensitivity in the state of low orientation.
  • the produced stencil sheet is preserved at a high temperature of about 50°C, for example, it is liable to induce the phenomenon of curling and, in an extreme case, the phenomenon of delamination.
  • the plate making is carried out by the use of a thermal head, the stencil sheet is liable to stick to the thermal head.
  • the stencil sheet is also disadvantageous in being deficient in resistance to the impact of printing and in resolution because it has conspicuously lower strength than the biaxially stretched film.
  • the method which comprises costretching a multilayer film combining a polyethylene terephthalate resin and a polypropylene resin, then heat-treating the costretched film at an elevated temperature in the range of 100° to 240 °C, for example, thereby thoroughly crystallizing the polyethylene terephthalate layer and imparting enhanced peeling property to the layer, and subsequently peeling and obtaining a film resistance to heat (useful as a thin-wall film for a condenser, for example) has been known to the art [Japanese Patent Application Disclosure SHO 60(1985)-178, 031].
  • the method which comprises subjecting the film of a similar layer combination to sequential biaxial stretching and then simultaneous biaxial stretching, subsequently heat-treating the stretched film at a temperature higher than the crystal melting point of polypropylene and lower than the crystal melting point of polyester thereby sufficiently promoting the crystallization of the polyester, and thereafter effecting the peeling has been known [Japanese Patent Application Disclosure SHO 61(1986) -31,236]. These methods are invariably based on the concept that since the peeling made during the course of stretching results in fracture of the film or in loss of uniformity of the film, the facility of peeling ought to be ensured by thoroughly carrying out the heat treatment mainly after the stretching thereby promoting the crystallization of polyester.
  • the invention described relates to a highly sensitive heat-sensitive film for stencil comprising a thermoplastic resin having a coefficient of temperature and melt viscosity ( ⁇ T/ ⁇ log VI) of not more than 100 and a thermal shrinkage (X%) at 100°C and a thermal shrinkage stress (Y g/mm2) at 100°C falling respectively in the ranges of the formulas; 15 ⁇ X ⁇ 80 and 75 ⁇ Y ⁇ 500 ; and both falling in the range of the formula; -8X+400 ⁇ Y ⁇ -10X+1000 ; having a thickness in the range of 0.5 to 15»m, and excelling in low-energy perforation property.
  • ⁇ T/ ⁇ log VI melt viscosity
  • X% thermal shrinkage
  • Y g/mm2 thermal shrinkage stress
  • the film of this invention highly effective in itself and is superior in a low temperature perforation property, capable of being perforated with a low energy thermal head or with a low energy flash irradiation for making a plate; expansion of perforations is small when the film is perforated; and its change with time (dimensional change) is small and its sizes are stable.
  • thermosensitive film In the technique of US 4766033 (especially Example 1), to facilitate stretching of the thermosensitive film, the film is made in multiple layers of which the thermosensitive film is central layer. However, since the thermosensitive film alone is peeled off and its film is laminated with porous supporting member, it is difficult to laminate, and further thermosensitive film easily tends to curl after laminate.
  • thermosensitive plate-making stencil sheet aims to provide a high-sensitivity thermosensitive multilayer film possing a flat smooth surface, having no possibility of sustaining qualitative defects such as scratches, wrinkles, warp, strain, float and fractures, and not entailing such adverse phenomena as curling and delamination and a stencil sheet capable of producing a plate for printing with high sensitivity and high resolution.
  • the inventors have continued various studies in search of a novel thermosensitive plate-making quality stencil sheet, to find that the stencil sheet aimed at is attained by superposing a functional layer (M) possessing specific properties found necessary during the course of plate making and printing desirably on either of the opposite surfaces of a specific peeling layer (P), further superposing a plate-making supporting layer (S) on the resultant composite of layers as an outermost layer contiguous to the functional layer and joining the layers by application of heat and pressure.
  • M functional layer
  • P specific peeling layer
  • S plate-making supporting layer
  • the present invention provides a high sensitivity thermosensitive costretched multilayer film comprising at least two functional layers (M) and at least one peeling layer (P), and having layer combination in which at least either of the outermost layers thereof is a functional layer (M) wherein said functional layers have a modulus of tensile elasticity of at least 196120kPa and consist of a thermoplastic resin layer possessing a thermal shrinkage ratio of at least 30%, a thermal shrinkage stress value in the range of 490 to 11,760 kPa (50 to 1,200 g/mm2), crystallinity of not more than 30% and a thickness in the range of 0.1 to 12 »m, said peeling layer contiguous to said functional layer possesses a Vicat softening point in the range of 30° to 120°C, contains at least one release agent, and consists of a different thermoplastic resin from that of said functional layer, and said two layers are easily peelable, peeling layer (P) exerts a compressive force by a compression strain in the range of 0.05 to 10
  • the present invention also provides a stencil sheet produced from the film and used for plate making, and a method for the production of the stencil sheet.
  • thermosensitive perforating stencil sheet obtained by attaching the porous supporting member to the costretched multilayer film consisting of the functional layer and the peeling layer and subsequently peeling the peeling layer is notably improved in terms of the efficiency of lamination of the film and the resistance of the plate-making stencil sheet to the phenomenon of curling over the countertype obtained by the lamination of single functional layer.
  • the film particularly with high perforation sensitivity is left standing for a long time especially at a relatively high temperature, it tends to curl and, in an extreme case, induce separation of the functional layer through delamination. This is mainly because the functional layer is liable to curl instantaneously immediately after the lamination owing to the tension exerted upon the film during the course of winding, whereas the porous supporting member kept in fast contact therewith is incapable of following this inclination.
  • the inventors have made various studies on this point, to find that generally desirable results are obtained by allowing the superposed composite of a plurality of layers inclusive of the functional layer in large collective thickness to be laminated with the supporting member and peeling the specific peeling layer from the produced film and that still better results are obtained by carrying out the costretching of the multilayer film in such a layer structure under such stretching conditions that the specific peeling layer contiguous to the functional layer is allowed to impart to the functional layer a compressive force proper for the functional layer. It has been further found that the aforementioned trouble is virtually completely prevented by subjecting the stretched costretched film to a suitable heatsetting treatment thereby imparting to the functional layer a compression enough to compensate for the shrinkage the functional layer is destined to sustain after the stretching.
  • the present invention provides a costretched multilayer film containing at least, two functional layers and at least one peeling layer, and having a layer combination in which at least either of the outermost layers thereof is a functional layer, characterized in that the functional layers consist of a thermoplastic resin layer exhibiting a thermal shrinkage ratio of at least 30%, a thermal shrinkage value of 490 to 11,760 kPa (50 to 1,200 kg/mm2), crystallinity of not more than 30% and possessing a thickness in the range of 0.1 to 12 »m, and the peeling layer contiguous to said functional layer possesses a Vicat softning point in the range of 30 to 120 °C, contains at least one release agent, and consists of a different thermoplastic resin from that of said functional layer, and said two layers are easily peelable, peeling layer exerts upon the functional layer at least one direction thereof a compression strain in the range of 0.05 to 10%.
  • the high-sensitivity thermosensitive multi layer film provided by this invention therefore, is such that the plate-making stencil sheet is vested
  • the term "functional layer” as used in the present invention refers to a resin layer adapted to record information therein by the perforation of pertinent lettering or image by virtue of the thermosensitive proprety of the resin.
  • the functional layer constitutes itself a resin layer which is intended to form a plate required, during the course of printing, to produce desired lettering, symbols, a photograph, or patterns on a surface given to be printed.
  • this layer is desirably formed of a substantially amorphous thermoplastic resin.
  • the thermoplastic resin which inherently has relatively high crystallinity and which, in the eventually formed multilayer film, assumes relatively low crystallinity, is embraced in the resin of the functional layer contemplated by this invention.
  • the material for the functional layer may be amorphous or crystalline thermoplastic resin.
  • the resin in the form contained in the finished film, is required to be in a substantially amorphous state exhibiting crystallinity of not more than 30%, desirably not more than 20%, and more desirably not more than 10% as measured by the density method.
  • the material for the functional layer is synthetic resin which, in a thoroughly annealed and equilibrium state exhibits the crystallinity mentioned above as determined by the DSC method.
  • this material is a resin which is constantly amorphous under ordinary conditions of production.
  • thermoplastic resins which answer the description given above include copolymerized polyester type resins, polyamide type resins, ethylenevinyl alcohol type copolymers, polycarbonate type resins, copolymerized polystyrene type resins, acryl type resins, vinyl chloride type resins, vinylidene chloride type copolymer resins, and polypropylene type resins, for example. These resins may be used either singly or in the form of a combination of two or more members (as a mixture or multilayer composite). The thermoplastic resins may be used mixed with other polymers, oligomers, plasticizers, etc.
  • copolymerized polyester type resin indicates a resin comprising two or more different species of either or both of the dicarboxylic acid moiety and the diol moiety of a polyester.
  • dicarboxylic acid moiety different species of the dicarboxylic acid moiety are used, combinations of terephthalic acid with other dicarboxylic acids such as, for example, aromatic dicarboxylic acids represented by isophthalic acid, phthalic acid, and 2,6-naphthalenedicarboxylic acid, aromatic dicarboxylic acids containing in the aromatic rings thereof substituents not contributing to the reaction of esterification, and aliphatic dicarboxylic acids represented by succinic acid and adipic acid are conceivable.
  • Two or more members selected from the group of dicarboxylic acids just mentioned may be used as the two or more species under discussion.
  • One preferred copolymerized polyester type resin is obtainable by preparing a diol moiety consisting mainly of ethylene glycol and additionally containing not more than 40 mol%, desirably 20 to 40 mol%, and more desirably 25 to 36 mol%, of 1,4-cyclohexane dimethanol and subjecting this diol moiety to polycondensation with a dicarboxylic acid moiety consisting mainly of terephthalic acid.
  • the raw material thus prepared in a thoroughly annealed and equilibrium state exhibits crystallinity of not more than 20% as determined by the DSC method.
  • the crystallinity is desired to be not more than 20%.
  • the material is desired to be in a substantially amorphous state (with crystallinity of not more than 10%), preferably a completely amorphous state.
  • Polyester which is not a copolymer can be used as the functional layer (M) by making it a film with crystallinity controlled in above-mentioned range.
  • One typical copolymerized polyester type resin answering this description is obtained by preparing dicarboxylic acid moiety consisting mainly of terephthalic acid and a diol moiety consisting of about 70 mol% of ethylene glycol and about 30 mol% of 1,4-cyclohexane dimethanol and copolymerizing these moieties.
  • the polyamide type resins which are usable herein include nylons 6, 66, 6-10, 11, and 12 and copolymerized nylons 6-66, 6-66-610 and 6-66-612, for example.
  • the copolymerized nylons prove particularly desirable.
  • these polyamide type resins copolymerized with a small amount of an aromatic dicarboxylic acid such as, for example, terephthalic acid, isophthalic acid or phthalic acid or an aromatic dicarboxylic acid containing a substituent making no contribution to the reaction of polymerization are also usable.
  • copolymers those which are obtained by suitably copolymerizing the aforementioned aromatic dicarboxylic acids prove desirable because they possess a rigid portion (effective in suitable improvement of the glass transition point) in the molecular structure and those obtained by copolymerizing a hydrocarbon moiety abounding with branches or a moiety possessing a saturated cycle or a polar group prove desirable because they are effective in lowering crystallinity and enhancing modulus of elasticity. With respect to the crystallinity, the rule already prescribed for the polyesters holds good on these copolymers.
  • the total proportion of such comonomers is generally not more than 30 mol%, preferably not more than 20 mol%.
  • the ethylene-vinyl alcohol copolymer is desired to possess an ethylene unit content in the range of 20 to 50 mol%, preferably 30 to 45 mol%.
  • the composition obtained by modifying the copolymer by incorporation therein of not more than 40% by weight of at least one resin selected from the group consisting of nylon type resins, polyester type resins, and ionomer type resins is also usable.
  • the polycarbonate type resins desirably use monomers liable to lower a softening point as compared with the conventional monmers or incorporate such monomers by copolymerization.
  • they may be produced in a form containing 5 to 40% by weight of other film-forming polymer.
  • copolymerized polystyrene type resins which are usable herein include those using acrylonitrile, acrylic esters, and diene type monomers as comonomers, for example.
  • those incorporating therein acrylic esters by copolymerization prove particularly desirable in terms of sensitivity.
  • the copolymerized polyesters prove particularly desirable in the sense that they possess sensitivity, strength, resistance to the impact of printing, and resistance to solvents in a balanced state.
  • thermoplastic resins of varying groups mentioned above may each incorporate therein not more than 50% by weight, based on the total amount of resin, of other polymer or oligomer.
  • additives such as, for example, fine powder of macromolecular compound, antioxidant, thermal stabilizer, plasticizer, macromolecular plasticizer, surfactant, slip additive, adjuvant, coloring agent, light-absorbing substance, filler of small specific heat, filler as good heat conductor in respective amounts incapable of impairing the properties required of the functional layer.
  • additives are silicones (liquid or particulate polymer), fluorine type polymer powder, silica, talc, calcium carbonate, carbon, graphite, alumina, various metals, and powdered oxides of such metals measuring 0.01 to 8 »m in average particle diameter.
  • the known monomers possessing such functions may be grafted to the resin of the functional layer (M) or to the surface region of the functional layer (M).
  • the thermoplastic resin incorporating therein a light-absorbing substance such as, for example, carbon, graphite, metal oxide, or coloring agent among other, additives mentioned above manifests heretofore unattainable outstanding effect and, as a synergistic effect with the specific polymer, a highly desirable perforating property.
  • thermoplastic resin to which above additives are added has same excellent effect regarding the super high speed plate-making which uses a solid laser, gas laser and others.
  • thermoplastic resin of which the functional layer is made is desired to possess a Vicat softening point measured in accordance with ASTM D-1525 (under a load of 1 kg at a temperature increasing rate of 2 °C/minute) in the range of 30° to 150 °C, desirably 40° to 130°C, and more desirably 50° to 120°C where the high performance in perforation is utilized to advantage.
  • thermoplastic film described above is usable not only for the thermosensitive plate-making stencil sheet but also as a paper for digital data recording and as a material for discs, sheets, and tapes or recording devices.
  • the material which has been perforated may be used as a filter material, a respiratory penetrating material, or a hygienic material, for example.
  • the functional layer of this invention is required to possess a modulus of tensile elasticity of at least 196120 kPa (20 kg/mm2), desirably not less than 294210 kPa (30 kg/mm2), more desirably not less than 490350 kPa (50 kg/mm2), still more desirably not less than 686490 kPa (70 kg/mm2), and most desirably not less than 980700 kPa (100kg/mm2).
  • the functional layer to be used possesses a modulus of tensile elasticity short of the lower limit mentioned above, there ensue many disadvantages that the film betrays weakness of nerve, the stencil sheet is so deficient in workability that it sustains elongation or fracture during the separation of the functional layer and the peeling layer, for example, the stencil sheet in storage is suffered to curl or delaminate with elapse of time, the film undergoes deterioration of dimensional stability or deformation or adhesion due to the pressure exerted during the course of plate-making step, and the stencil sheet suffers from such adverse phenomena as elongation and fracture during the course of printing.
  • the modulus of tensile elasticity is determined by the method specified in ASTM D 882-67 and is reported on the basis of the stress for 2% elongation taken as a modulus of 100%.
  • the functional layer is further required to possess a thermal shrinkage stress value in the range 490 to 11760 kPa (50 to 1200 g/mm2), desirably in the range 740 to 11760 kPa (75 to 1,200 g/mm2), and more desirably in tie range of 980 to 9800 kPa (100 to 1,000 g/mm2).
  • the thermal shrinkage stress value is determined by cutting, a strip 10 mm in width from a sample film containing the functional layer, setting the strip of film in place kept taut with the opposite ends thereof nipped in chucks each fitted with a strain gauge and separated from each other by a distance of 50 mm, immersing the sample film in silicone oil heated to varying temperatures and detecting the stress generated consequently in the sample film.
  • the value of stress is taken at the end of 10 seconds' immersion in the silicone oil when the oil temperature does not exceed 100°C and at the end of 5 seconds' immersion when the oil temperature exceeds 100 °C.
  • the value of stress is taken in the direction of stretching.
  • the film For a biaxially stretched film, the average of two values of stress taken in the longitudinal and lateral direction is recorded. (This method of reporting will apply invariably hereinafter.)
  • the film is desired to be biaxially stretched.
  • the film is rated as conforming to the present invention so long as some if not all of the values of shrinkage stress taken at varying temperatures fall in the range defined above.
  • the shrinkage stress value in the aforementioned range is desired to be manifested at a temperature in the range of 60 to 150°C, desirably 60° to 140°C, more desirably 70° to 120 °C, and most desirably 70° to 110 °C.
  • the lower limit, 490 kPa (50 g/mm2) fixed for the thermal shrinkage stress value constitutes itself an essential basic property for efficient perforation to be made in the paper. If the thermal shrinkage stress value is smaller than this lower limit, the efficient perforation is not easily obtained by the thermal head method, for example. If this value exceeds 11760 kPa (1,200 g/mm2), the perforation tends to produce unduly wide bores, the film sustains strain, the paper curls, and the resolution is liable to degrade. If the shrinkage stress value is manifested at an unduly low temperature, there arise disadvantages that the resolution is degraded and the paper is suffered to curl because the dimensional stability is degraded and the perforation produces excessively wide bores. If the value is manifested at an unduly high temperature, there ensues a disadvantage that the sensitivity of perforation is degraded.
  • the film is required to possess a thermal shrinkage ratio of not less than 30%, desirably in the range of 30 to 90%, and more desirable in the range of 40 to 80%.
  • This thermal shrinkage ratio is determined by cutting from a given film a sample of the square of 50 mm, placing the sample film in a constant temperature bath set at a prescribed temperature, treating it therein for 10 minutes in a state allowed to shrink freely, finding the amount of shrinkage of the sample, and calculating it in percentage based on the original size.
  • the thermal shrinkage ratio in the aforementioned range is desired to be manifested at a temperature in the range of 60° to 170°C, desirably 60° to 160°C, more desirably 60° to 150 °C, and most desirably 65° to 140 °C. If the thermal shrinkage ratio is less than 50%, the efficient perforation is not easily obtained, the sensitivity degrades, and the dimensional stability and the resolution are liable to decline. Conversely, if the thermal shrinkage ratio exceeds 90%, the resolution and the dimensional stability are impaired and the stencil sheet is suffered to curl because the perforation produces unduly wide bores and the film sustains strain.
  • the functional layer in the stencil sheet of this invention has a thickness in the range of 0.1 to 12 »m, desirably 0.3 to 8»m, and more desirably 1 to 6 »m. If this thickness is less than 0.1 »m, the produced paper does not fit practical use because it is difficult to handle, deficient in strength, liable to produce excessively wide bores in perforation, and apt to sustain fracture during the course of perforation and exhibit insufficient resolution. Conversely, if the thickness exceeds 12 »m, the facility of perforation is lowered and the workability is degraded.
  • the functional layer is desired to have a thickness in the range of 0.3 to 5 »m, desirably 0.5 to 4 »m, more desirably 0.6 to 3 »m, and most desirably 0.7 to 2 »m.
  • the functional layer may be used not in a state superposed on the porous supporting member but in the form of a selfsupporting structure obtained by being superposed on a peelable base sheet of irregular surface, perforated, and then peeled or in the form perforated as applied on a platen roll of irregular surface.
  • the thickness of the functional layer is desired to be in the range of 5 to 12 »m, though it is not required to be specifically defined.
  • the functional layer in this invention is formed in a single-layer structure.
  • it may be formed in an at least two-layer structure by being superposed on one member selected from the group consisting of sensitizer layer, sensitivity adjusting layer, lubricant layer, hotmelt layer, antisticking layer, strength enhancing layer, dimensional stabilizer layer, and optical perforation layer.
  • the peeling layer in the stencil sheet of the present invention is required primarily for the impartation of highly desirable properties to the stencil sheet during the course of the stretching step. It is further useful for ensuring efficient transfer of additives to the functional layer as well as for protecting the surface of the functional layer and reinforcing the stencil sheet to withstand the impacts of handling and fabrication. It is destined to be peeled after the lamination of the film with the supporting member is completed or immediately before the plate-making step. This peeling layer, therefore, is required to be formed of a material easily peelable from the functional layer. This peeling strength of the peeling layer from the functional layer should not be such that the peeling of the peeling layer occurs during the course of stretching, lamination, or other work of handling.
  • the peeling layer fulfils the role of enabling the film to be smoothly stretched under the conditions under which the functional layer in its independent form would not be easily stretched and endowing the film with the compressive force for compensating the shrinkage force that the stretched functional layer assumes with the elapse of time.
  • the material for the peeling layer is a polyolefin type resin which exhibits a Vicat softening point of not more than 120°C, desirably not more than 110 °C, a crystal melting point not more than 160 °C and crystallinity in a thoroughly annealed state (determined by the DSC method) of not more than 60%.
  • the polyolefin type resins which are usable herein include ethylene type polymers, copolymer consisting of ethylene and a monomer having a polar group, ethylene- ⁇ -olefin copolymers, propylene type copolymers of relatively low crystallinity, polybutene-1 type copolymers, and copolymers of various polyolefins, for example.
  • ethylene type polymers copolymer consisting of ethylene and a monomer having a polar group
  • ethylene- ⁇ -olefin copolymers ethylene- ⁇ -olefin copolymers
  • propylene type copolymers of relatively low crystallinity polybutene-1 type copolymers
  • copolymers of various polyolefins for example.
  • the crystallinity is expressed as the sum calculated based on the mixing ratio of the component resins of the mixture.
  • Vicat softening point of a mixture is indicated at the value as measured in the mixture condition.
  • a mixture consisting mainly of a polyolefin type resin may be usable as the material for the peeling layer, and the polyolefin type resin containing up to 50% by weight of other thermoplastic resin may be desirably usable as the material for the peeling layer.
  • a mixture consisting mainly of an ethylene type copolymer and incorporating therein 5 to 50% by weight of an ethylene- ⁇ -olefin elastomer copolymer and a mixture consisting of 100 parts by weight of the mixture just mentioned and 5 to 100 parts by weight of a polypropylene type polymer may be used.
  • the ethylene type copolymers which are usable herein include ethylene-vinyl acetate copolymers (EVA) containing 5 to 25% by weight of vinyl acetate unit, copolymers of ethylene with a monomer selected from the group consisting of unsaturated aliphatic monocarboxylic acids and esters thereof, ionomer resins thereof, linear low-density polyethylene (LLDPE), very low-density polyethylene (VLDPE), and mixtures thereof, for example. More desirably, the ethylene type copolymers are LLDPE and VLDPE.
  • the permissible amount of additive is small, the uniformity of bleeding is impaired and the peeling property is jeopardized unless the heat-treatment is performed sufficiently.
  • the polymer or copolymer is used by the two-step bubble tubular stretching method, the nipped edges of the film before the stretching and the interface between the layers during the course of stretching are liable to sustain strain, possibly with the result that the separation occurs between other layers. This trend occurs particularly conspicuously when the stretching is performed by external force, for example performed by the tenter method.
  • the sequential biaxial stretching method separation between layers and non-uniform stretching are liable to occur in the portions nipped by the tenter clips.
  • thermoplastic resin used as the peeling layer is in the range from 30 to 120°C. If the Vicat softening point is lower than 30°C, the resin itself acquires an adhesive effect and renders the peeling difficult. If this temperature exceeds 120 °C, the resin is troubled with the problem about the behavior of additive bleeding.
  • the functional layer can easily be partially peeled and damaged since it becomes too hard to absorb partial strain during various operations and moreover the whole multilayer body of the functional layer and the peeling layer becomes more prone to tearing.
  • thermoplastic resin possesses in itself a satifactory stretching property and aids in the stretching of the other resin layer adjoining it and precludes the possible occurrence of the phenomenon of necking with the other resin layer in consequence of the stretching. While the costretching of the laminate is in process, the tight inter layer adhesive force manifests itself synergistically with the action of the additive to prevent the component layers from mutual separation. The synergistic effect is manifested in widening the range of optimum stretching conditions and facilitating the stabilization of the film. As the result, the stretching properties of the produced film such as the strength of the combined layers are improved and the stretching property of the functional layer is similarly improved.
  • thermoplastic resin or composition of which the peeling layer is formed in the light of the stretching property of the multilayer film incorporating the peeling layer by superposition, the compressive property of the peeling layer, the peeling layer's property with respect to bleeding of additive, and the affinity of the resin or composition for the other resin, is desired as a raw material to possess crystallinity of not more than 60% as determined by the DSC method.
  • the costretching cannot be smoothly performed when the optimum stretching condition for the resin or composition of the peeling layer differs widely from that for the resin off which the funtional layer is formed. It is, therefore, advantageous to use as the raw material for the peeling layer a resin which possesses a Vicat softening point not defferent by more than 100 °C from that of the resin for the functional layer.
  • the peeling layer is capable of exerting upon the functional layer in at least one direction thereof a compressive force producing a compression ratio in the range of 0.05 to 10%.
  • This compressive force may be generated from the resin layer in an independent from, i.e. from the single-layer structure or from an arbitrary layer in the combination of two or more resin layers, i.e. the composite structure, in an arbitrary amount.
  • the resin in the form of an amorphous polymer or copolymer possessing a Vicat softening point not less than 10°C lower than the stretching temperature, desirably higher than the stretching temperature, and especially at least not less than 10 °C higher than the stretching temperature forms a continuous phase.
  • the resin in the form of a crystalline polymer or copolymer possessing a melting point 2°C ⁇ 40°C higher than the stretching temperature and especially 5° to 30 °C higher than the stretching temperature or in the form of a mixture of two or more such polymers or copolymers is desired to form a thermoplastic resin composition of continuous phase.
  • the resin of the continuous phase is desired to be in a proportion of riot less than about 50% by volume, preferably not less than 60% by volume.
  • the thickness of the peeling layer (P) on account of the relation with the bleed out of additive and the compressive force, falls generally in the range of 2 to 20 »m, preferably in the range of 3 to 12 »m.
  • the modulus of tensile elasticity of the single layer is desired in the range of 49040 to 588420 kPa (5 to 60 kg/mm2). If the modulus is less than the lower limit of this range, the produced peeling layer is excessively soft and the compressive force and the facility of peeling are disadvantageous, for example. If the modulus exceeds the upper limit the peeling layer is notably deficient in the compressive force and the amount of compression, the facility of peeling, and the peeling during the course of stretching.
  • the peeling layer When the peeling layer is to be formed in a composite structure as generally desired, it is desirable to superpose on the peeling layer (P) at least two of the resin layers of severally different functions such as, for example, a resin layer serving the purpose of preventing the peeling layer from sustaining damage during the course of the peeling following the stretching step, a resin layer for effecting the transfer of additive bleed to the functional layer, and a resin layer for exertion of a proper compressive force on the functional layer.
  • a resin layer serving the purpose of preventing the peeling layer from sustaining damage during the course of the peeling following the stretching step
  • a resin layer for effecting the transfer of additive bleed to the functional layer and a resin layer for exertion of a proper compressive force on the functional layer.
  • the proportion of additive bleed, the uniformity of peeling, and desirably the control of the compressive force can be facilitated.
  • the P B layer which mainly combines flexibility, ability to contain the additive, and ability to effect additive bleedout can be cited.
  • the layer of the aforementioned thermoplastic resin or composition to be used in the single-layer structure mentioned above the (P B1 layer: referred to hereinafter as "main peeling layer") and the layer of an olefin type polymer or copolymer possessing a melting point lower than the stretching temperature or a composition consisting mainly of the polymer or copolymer (P B2 layer) are included in the category of P B mentioned above.
  • Desirable examples of the P B include the aforementioned EVA, ethylenically unsaturated monocarboxylic acids and derivatives thereof, and soft ethylene- ⁇ -olefin copolymers, for example.
  • the layer of an amorphous polymer or copolymer possessing a Vicat softening point not less than 10°C lower than the stretching temperature or a composition consisting mainly of the polymer or copolymer (included as P B3 in the aforementioned category of P B ) is another example.
  • the P B layer is desired to possess a modulus of tensile elasticity of not more than 490350 kPa (50 kg/mm2), preferably in the range of 49040 to 392280 kPa (5 to 40 kg/mm2). If the modulus of tensile elasticity exceeds the upper limit of the range, the produced peeling layer proves unsatisfactory with respect to fitness to the functional layer (M), abnormal delamination during the course of fabrication, compressive force, amount of compression, behavior of additive bleeding, and facility of peeling of the thin functional layer (M).
  • the P B layer is formed so as to adjoin the functional layer (M)
  • the interlayer disturbance with the functional layer (M) is prevented
  • the peeling is allowed to proceed smoothly at a high speed (100 to 200 m/minute) throughout the entire surface, and the possibility of the P A layer eating into the functional layer(M) and sustaining fracture the P A layer adjoin the functional layer (M) is precluded.
  • the layer of a polymer or copolymer of the polypropylene type possessing a crystal melting point generally higher than the stretching temperature and a Vicat softening point of not lower than 120 °C or a composition consisting mainly of the polymer or copolymer is used as an assisted peeling layer (P A ).
  • Group (I) combination of layers in the multilayer peeling layer consists of at least one layer selected from among the aforementioned P B1 , P B2 , and P B3 layers and at least one P A layer.
  • the layers selected from among the P B1 , P B2 , and P B3 are disposed on at least either, preferably both, of the opposite surfaces the P A layer.
  • the favorable arranging example of layers in this case is to arrange the aforesaid resin or the composition of resin having softer modulus of tensile elasticity (49040 to 490350 kPa (5 to 50 kg/mm2)) than (P A ) layer at least on one side of the (P A ) layer possessing the harder modulus of tensile elasticity to be mentioned later and the reason for this is as described as follows.
  • the functional layer (M) is desired to adjoin the layers selected from among the P B1 , P B2 , and P B3 .
  • Group (I I ) combination of layers consists similarly of at least one P B1 layer and at least one layer selected from between the P B2 and P B3 .
  • the order of arrangement of the component layers in this combination is arbitrary.
  • the resin layer capable of easily containing a release-promoting additive and readily bleed the contained additive is disposed to adjoin the functional layer.
  • the layer combination of Group (I ) include P B1 /P A , P B2 /P A , P B3 /P A , P B1 ,/P A /P B1 , P B2 /P A /P B2 , P B3 /P A /P B3 , P B1 /P A /P B2 /P B1 /P A /P B3 , and P B2 /P A /P B3 .
  • other layers may be freely incorporated in the combinations mentioned above.
  • the combination of Group (II) include P B2 /P B-1 /P B3 /P B1 , P B1 /P B2 /P B1 , and P B1 /P B3 /P B1 , preferably P B2 /P B1 /P B2 , P B3 /P B1 /P B3 , and P B2 /P B1 /P B3 .
  • other layers may be freely incorporated in the combinations mentioned above.
  • the thermoplastic resin of which the assisted peeling layer (P A ) intended for reinforcement is formed is desired to possess a Vicat softening point of higher than 120°C, desirably not lower than 130°C, and more desirably not lower than 135 °C, and modulus of tensile elasticity of not less than 490350 kPa (50 kg/mm2), and desirably not less than 686490 kPa (70 kg/mm2).
  • Propylene type polymers for example, are advantageously usable as such thermoplastic resins.
  • the propylene type polymers may be homopolymers or copolymers or mixtures thereof with not more than 40% by weight of other polymers such as, for example, polybutene-1.
  • thermoplastic resins include polybutene-1 type polymers and copolymers methylpentene type polymers and copolymers and compositions thereof, and other similar arbitrary polymers copolymers and compositions thereof.
  • these thermoplastic resins are used as mixed with 40 to 5% by weight of soft polymers or copolymers. The combination is especially effective in imparting a proper amount of compression to the functional layer (M).
  • soft polymers and copolymers usable for the mixture mentioned above elastomeric resins and rubbery resins prove particularly desirable. They include such known resins as ethylene- ⁇ -olefin copolymers, for example. It is essential that the layer of such a soft resin should be capable of being costretched with the other component layers including the functional layer (M) and capable of effectively imparting the aforementioned amount of compression.
  • the adhesive strength between these layers should be greater than the adhesive strength between the functional layer and either of the two layers mentioned above.
  • the thicknesses of the component layers of the peeling layer of multilayer structure are not particularly restricted.
  • the thickness of the P A layer is in the range of 0.5 to 20 »m, preferably 1 to 10 »m.
  • the thickness of the P B1 layer or the thickness of the layer selected from between the P B2 and P B3 expressed as a single thickness when the layers are used independently of each other or as a combined thickness when they are used in a multilayer state generally falls in the range of 1 to 20 »m, preferably 2 to 10 »m, in the light of the relation with the additive bleedout and the impartation of desired compressive force.
  • the peeling layer contemplated by the present invention must incorporate therein a suitable release agent to ensure smooth removal of the peeling layer from the functional layer, prevent the peeling layer from being accidentally removed from the functional layer during any of the steps other than the step of peeling, and allow the entire process to proceed smoothly.
  • the release agents which answer the description include esters of higher fatty acids with polyhydric alcohols, esters of higher fatty acids with polyoxyethylene type alcohols, nonionic surfactants such as polyoxyethylene alkyl ethers, higher alcohols and esters thereof, higher fatty acid amides, waxes, oligomers, silicone oils, fluorine type oils, and fluorilicate type macromolecular compounds, for example.
  • release agents mentioned above those which are in the liquid state at normal room temperature and possess a viscosity of not less than 100 mPa.s (100 c. poises) at 50 °C prove particularly desirable for the purpose of imparting a suitable peeling property. They are allowed to assume a pasty state at normal room temperature and desired to possess a melting point of not higher than 50°C.
  • the viscosity may be that of a single release agent used alone or that of a mixture of two or more release agents used jointly.
  • an antistatic agent, an antisticking agent, etc. may be added independently of one another or jointly with one another.
  • the amount of the release agent to be added is generally in the range of 0.2 to 5% by weight, based on the total weight of the thermoplastic resin of which the peeling layer is formed.
  • the release agent incorporated in the prescribed peeling layer after the peeling layer is superposed on the functional layer and the two a layers costretched, quickly bleeds to the surface of the peeling layer and facilitates the separation between the functional layer and the peeling layer.
  • the test for peeling strength between the peeling layer and the functional layer is carried out by peeling a sample test piece in the T-shape pattern by the aforementioned tensile test method, with the speed of tension fixed at 200 mm/min [Japanese Industrial Standard (JIS) K 6854].
  • the peeling strength is generally not more than 1.96Nm ⁇ 1(2 g/cm)of width, preferably not more than 0.98Nm ⁇ 1(1 g/cm)of width.
  • the peeling strength between the functional layer and the composite peeling layer as a whole is the same as that described above.
  • the peeling strength between the P B and P A layers must be greater than that between the functional layer and the P B layer so as to inhibit separation between the P B and P A layers.
  • the peeling strength under discussion is desired to be not less than 4.9Nm ⁇ 1(5 g/cm) of width, preferably not less than 9.8Nm ⁇ 1(10 g/cm)of width.
  • the acceleration of the speed of separation is attained advantageously by incorporating in the peeling layer a mixture of an oleic acid monoglyceride and a polyglycerin monooleate (prepared in mixing ratio of former/latter in the range of 1:4 to 4:1) in a proportion in the range of 0.5 to 3.0% by weight, based on the total weight of the peeling layer.
  • the peeling layer of this invention when necessary, may incorporate therein in addition to the release agent mentioned above various additives for improving the physical properties of the peeling agent and may further incorporate a layer adjoining the peeling layer and modifying the surface property of the functional layer.
  • various additives for improving the physical properties of the peeling agent and may further incorporate a layer adjoining the peeling layer and modifying the surface property of the functional layer.
  • the incorporation of an amino-modified silicone, a mercapto-modified silicone, or an epoxy-modified silicone as an antisticking agent in a small amount (such as, for example, 0.1 to 3% by weight) proves advantageous.
  • the peeling layer in the multilayer film of the present invention exerts upon the functional layer in at least one direction thereof a compressive force producing compression strain suitable but not so large as to impair the planarity of the functional layer.
  • the compressive force is exerted simultaneously in the longitudinal and lateral directions.
  • the expression "not impair the planarity" as used herein means that the functional layer of the film is not compelled by the compressive force to fold itself in a zigzagging force and entail the phenomenon of blushing.
  • the amount of compression strain determined by the method to be described specifically hereinafter is required to be in the range of 0.05 to 10%, desirably 0.1 to 5%, and more desirably 0.2 to 3%.
  • this ratio of compression is less than 0.05%, the phenomenon of curling (which possibly occurs after the multilayer film is superposed on the porous supporting member and then the peeling layer is peeled) cannot be fully precluded.
  • the compression ratio exceeds 10%, the multilayer film itself succumbs to the phenomenon of abnormal peeling and entails the phenomenon of blushing and the functional layer suffers the planarity thereof to be impaired after the removal thereof from the peeling layer subsequent to the super-position thereof on the supporting membrane and, moreover, the plate eventually produced entails the disadvantage that the uniformity of quality is jeopardized and the plate itself curls toward the supporting member side. This amount of contraction of compression strain does not always equal the amount of contraction which occurs after the superposition.
  • the determination of the amount of compression is carried out by stretching a given multilayer film under prescribed conditions, removing the functional layer from the stretched film in the manner to be described hereinbelow, and performing a pertinent measurement on the removed functional layer.
  • the return of the functional layer to the original size after the removal from the film originates in the compressive force which the peeling layer exerts upon the functional layer after the stretching.
  • the ratio of compression of the functional layer can be controlled by varying the thickness of the peeling layer of a single-layer structure or the thicknesses of the component layers of the peeling layer of multilayer structure or by adjusting the stretching conditions and the heat setting conditions, for example.
  • the optimum magnitude of the amount of compression varies with the purpose for which the multilayer film is utilized or with the kind of the functional layer (M). In the case of a material of relatively low modulus of tensile elasticity or a soft material, for example, it is convenient to fix this magnitude at a slightly larger level. Generally, however, this magnitude is fixed in the aforementioned range.
  • the stretching conditions for the multilayer film have a direct effect on the performance of the functional layer and can be controlled by the heat-setting conditions after the stretching. In this case, it is convenient to use fixed values and employ the temperature of the heat setting aimed at a fixed amount of relaxation as a factor.
  • the relation between the functional layer and the peeling layer with respect to thermal shrinkage can be estimated by the determination of the temperature dependency of their elongation-contraction properties, namely the dependency of the ratio of shrinkage and the contractive stress.
  • the ratio of shrinkage of the peeling layer under the conditions of heat treatment must be greater than that of the functional layer. If this relation is reversed, the functional layer sometimes if not always exerts compression on the peeling layer. In this case, the resistance to the phenomenon of curling is rather jeopardized than improved.
  • the method to be adopted for the production of the multilayer film of this invention is not specifically restricted.
  • the production can be carried out by any of the known methods generally adopted for the production of any ordinary multilayer film.
  • the production is attained by melting the raw materials for the functional layer and the peeling layer in separate extruding machines, coextruding the molten raw materials through annular or T-type multilayer dies, suddenly cooling the extruded sheets of molten raw materials, and stretching the cooled sheets by the tenter method or the bubble method.
  • the stretching temperature (namely, the temperature of the part at which the stretching is started) to be selected should be capable of imparting a prescribed orientation to the functional layer formed of the specific resin and the peeling layer of single-layer structure is formed of the aforementioned resin and caused to incorporate therein the additives found necessary.
  • the peeling layer of multi layer structure it suffices to select resins and a layer combination as described above and, for the particular one of the component layers which adjoins the functional layer, select a resin incorporating therein necessary additives.
  • the stretching temperature generally is in the range of 60° to 150°C, desirably 70° to 130°C, and more desriably 80° to 120 °C.
  • the stretching is desired to be performed biaxially at a ratio approximately in the range of 4 to 49 times, preferably 8 to 36 times, the original surface area.
  • the material and thickness of the peeling layer are designed and the stretching conditions and the heat setting conditions are controlled so that the peeling layer will exert a prescribed compressive force upon the functional layer.
  • the bubble method proves particularly advantageous in the sense that it is capable of easily producing a high-sensitivity film by a simultaneous biaxial stretching operation at a high speed of transformation efficiently in a large volume.
  • the stretching is effected by applying an external force to the terminal parts of the superposed layers, the stretching is liable to entail mutual deviation between the layers and abnormal peeling.
  • These abnormal phenomena occur particularly conspiqicuously in a sequential biaxial stretching operation and the produced film is short of the tolerable level for this invention.
  • the allowable ranges for the stretching conditions (temperature, speed, and stretching ratio), therefore, are narrowed, rendering the production of a film of desired properties difficult. It also becomes difficult to ensure efficient impartation of peeling property, compressive force, and amount of compression.
  • the bubble method is not troubled with these adverse phenomena because the stretching force generated by the internal pressure is allowed to act uniformly on the entire surface.
  • the multilayer film of this invention consists of at least one functional layer and at least one peeling layer.
  • This peeling layer may be in a single-layer structure or in a multilayer structure.
  • M functional layers
  • P peeling layers
  • This multilayer film has a layer combination in which at least either, preferably both, of the outermost layers thereof is a functional layer.
  • the film inclusive of the opposite surface layers and the intermediate layers is desired to have a symmetrical layer structure.
  • the production of the high-sensitivity thermosensitive plate-making stencil sheet by the use of the multilayer film of this invention is attained by superposing plate-making quality supporting member at least one of the functional layers of the multilayer film and separating the film along the interface between a functional layer and a peeling layer thereof thereby giving rise to the paper aimed at.
  • the production is effected by preparing the multilayer film in such a manner that the peeling layer will exert the prescribed amount of compression on the functional layer, effecting the superposition of the supporting member as described above, and performing the aforementioned separation of the film thereby relieving the functional layer (M) of the compressive force.
  • an ink-pervious porous film or sheet adapted to meet the purpose for which the paper is intended or a base paper possessing a rugged surface can be used.
  • the supporting layers of the former class include Japanese paper and plain paper of the form of onion paper having a basis weight in the range of 3 to 15 g/m2 and similar sheets of synthetic fibers, natural fibers, regenerated fibers, and mixtures thereof, for example.
  • a mesh-screen type woven fabric formed of long fibers is another example.
  • the mesh-screen type woven fabric has a mesh size approximately in the range of 2 to 20 openings/mm (50 to 500 meshes), preferably 3 to 12 openings/mm (70 to 300 meshes).
  • the base paper possessing a rugged surface convenient for the sake of perforation may be cited as the specific supporting member, which is used in combination with a functional layer of relative large thickness approximately in the range of 6 to 18 »m with a peeling layer, for example, to form a laminate (for perforation), then the base paper with the functional layer peeled from the peeling layer, the functional layer is perforated with dot-like discrete holes arranged in a prescribed pattern, and put to use in printing in a state supporting thereon given information.
  • the base paper thus used has minute projections and depressions, specifically projections, arranged regularly,
  • the projections have a cross section of the shape of a circle, a rectangle, an ellipsis, a line, or continued meshes. These projections may be randomly laid. Preferably, they are regularly arranged. Generally, these projections have a height of not than 15 »m, desirably not less than 25 »m, and more desirably not less than 30 »m. In the case of discrete projections, the individual projections have a size in the range of 2.5 ⁇ 10 ⁇ 5 to 1.44 ⁇ 10 ⁇ 2 mm2 The propotion of the available surface area of the projections is approximately in the range of 1 to 35%.
  • projections constitute themselves in the portions of the base paper to be joined by lamination with the functional layer in a readily separable state.
  • the projections may be formed of the same material as the base paper of sheet or film by embossing, for example. Otherwise, they may be formed by the printing or resist method of patterning on the surface of film, sheet, paper, or fiber.
  • the supporting member described above is joined with the functional layer by the use of an adhesive agent or by thermal fusion or some other means.
  • the adhesive agent to be used for the lamination is not specifically restricted. Any of the conventional adhesive agents may be used.
  • the adhesive agents which are usable herein include an adhesive agent to be used as dissolved in a solvent ,an adhesive agent of the form of emulsionretex, an adhesive agent of a hot melt form, a powdery adhesive agent, adhesive agents of reaction hardening type resorting to the action of water, the mixture of two components, or the exposure to ultra-violet light or electron beam, and adhesive agents relying on the combination of such functions such as, for example, an adhesive agent of hot melt type having the consistency of emulsion, an adhesive agent vested with the function of emulsion, an adhesive agent vested with the function of emulsion in combination with the function of curing agent, and an adhesive agent formed by combining a solution of adhesive agent in a solvent and a reaction hardening type adhesive agent.
  • the amount of the adhesive agent to be used, as reduced to the solids content after the adhesion, is generally in the range of 0.1 to 8 g/m2, desirably 0.2 to 5 g/m2, and more desirably 0.3 to 3 g/m2 .
  • the method for the lamination is not specifically restricted. Any of the methods generally used for lamination may be selected to suit the kind of the adhesive agent to be used. This lamination is only required to join the desired supporting member to the thermoplastic resin film as the outermost layer of the multilayer film. For the application of the adhesive agent, a coating roll provided with a doctor knife is used, for example.
  • the multilayer film is superposed on the prescribed supporting layer.
  • This supporting layer must adjoin the functional layer constituting itself the outermost layer of the multilayer film.
  • a plurality of plate-making quality papers can be obtained at one time by joining the supporting member (S) to the functional layer (M) constituting itself the outermost layer, separating the superposed composite (plate-making stencil sheet consisting of the supporting layer and the functional layer, removing the peeling layer (P), performing the procedure described above on the functional layer (M) possessing an exposed surface, and sequentially repeating the procedure of peeling the superposed composite (plate-making stencil sheet) consisting of the supporting layer and the functional layer.
  • S stands for a porous supporting layer.
  • the multilayer film comprising the functional layer and the peeling layer is first prepared, and the paper-making stencil sheet aimed at is produced by laminating the supporting layer superposed on one of the opposite surfaces, or sequentially or simultaneously on both of the opposite surfaces and peeling from the peeling layer.
  • thermosensitive plate-making stencil sheet to be obtained by the method of this invention has a flat smooth film surface, has the feedom from scratches, wrinkles, warp, strain, and fractures as compared with the countertype obtained by the conventional method, and enjoys high sensitivity and high resolution and uniform quality. It can be advantageously utilized in a plate-making system which perforates information at a high speed with a low energy source.
  • the method of this invention is advantageous in that (1) it enables the supporting member to be uniformly superposed by lamination on a film of small thickness approximately in the range is not attained by the conventional method; (2) the lubricating treatment and the antistatic treatment for the film surface of the plate-making quality paper can be automatically effected by the bleeding from the peeling layer; (3) the phenomenon of curling otherwise generated in the plate-making quality paper owing to the time-course in consequence of the enhancement of sensitivity can be precluded substantially completely; (4) a plurality of plate-making quality papers can be obtained from one multilayer film; (5) the multilayer film having functional layers superposed one each on the opposite surfaces of the supporting member each through the medium the peeling layer can be used in its unaltered form as a finished product and is only required to be separated immediately prior to use and, therefore, the plate-making quality papers obtained therefrom the multilayer film are perfectly free from the phenomenon of curling, scratches, and dirt; (6) the lamination is carried out inexpensively; and (7) the peeling layers removed from the multilayer film can be
  • Perforating sensitivity is determined by printing pressure energy (mjoule) per dot when a given plate-making stencil sheet is perforated at regulated printing pressure energy by line-type thermal head of plate-making part of plate-making type automatic printer.
  • Type 007 DPF manufactured by Riso Kagaku Sha optical density of solid black part (stable part of 5mm square solid black part of the original which is printed under standard conditions i.e. medium point of original density measure by making plate at original select letter mode) is measured by handy-type density meter DM-800 manufactured by Dainippon Screen Manufacturing Co. Ltd., and its value is not less than 1.0 when standard black sample (optical density 1.72, DIN 16536, type 47 B/P) is blank.
  • a given film sample is placed on a flat glass board, a Japanese paper of the form of onion paper made of polyester with good dimensional stability (METSUKE 12g/m2) is glued to the film by using 10 wt% methanol solution of vinylacetate type glue, and after drying, the sample is fixed with inside measurement 10cm ⁇ 10cm frame.
  • Two cutlines are made on the film diagonally so that the two lines cross at a right angle, the sample is left for one month at a given temperature, it is conditioned in the room with constant temperature of 23 °C and humidity 50 % RH for approximately 2 hours, and curling degree R is calculating by measuring radius r(mm) of the curl in vertical direction and horizontal direction and applying formula below. Though this curling degree should ideally be 0, practical allowable limit is about 7 to 8 and value more than 15 will made the product impractical. Delamination phenomena can after be seen if the curling degree exceeds 20.
  • Compression volume of the functional layer is determined by percentage of length of the film stretched,, to that of the original multilayer film when a given multilayer film which is cut out to be 1000mm ⁇ 50mm is aged for 24 hours in the room with constant temperature of 23 °C and relative humidity of 50% RH and measure functional layer after peeling from the peeling layer.
  • Each of the functional layer (M1), the peeling layer (P B2- 1) and the assisted layer (P A- 1) is fused by extruder and after extruding is completed so that structure of each layer may be M1/P B2- 1/P A- 1/P B2- 1/M1 from ring shape multilayer die, the layers are quenched to become hardened through refrigerant. Tube shape original roll is accordingly obtained.
  • this original roll is stretched to be bubble shape by being stretched in two directions simultaneously at stretching temperature of 102°C under the atmosphere so that resulted stretching rate may be 5.0 vertically and 5.0 horizontally and cooled by air at 20 °C.
  • Two edges of the film obtained above are slit and as result two films can be rolled by rewinders.
  • smooth stretching was conducted stably without shaking or puncture of bubble, and the film achieved is homogeneous.
  • no peeling (at niproll) occurred between layers prior to stretching or no partial peeling phenomenon can be seen at all.
  • Thickness of each layer of this multilayer film was 2/8/2/8/2 (»m). Compression volume of the functional layer was 1.1 % on average of vertical and horizontal direction.
  • M1/P A-3 /M1 which is combination of P A- 3 consisting of copolymer polypropylene only and layer M1 saw a lot of bubble shaking and puncture and could not be stretched homogeneously. Partial peeling prior to stretching occurred particularly at a part which is nipped by and slippage between layers and peeling during stretching often took place. Because of interlayer disturbance between layers M1 and P A- 1 one layer cuts into the other and thus the phenomenon was seen wherein layer M1 was torn at time of peeling.
  • a similar study was made as a comparative example on layer structure of M1/P A- 3/P B2- 1/P A- 3/M1. The result was of lower quality compared with the examples, and peeling phenomenon was apparent before and during stretching as seen in the previous comparative example as well as disorder between layer M1 and other layer and a lot of tearing of layer M1 at time of peeling.
  • polyester fiber fiber diameter 45 »m
  • secondly Japanese paper made of Manila hemp with Metsuke 8.7 g/m2 was used while as an adhesive agent ethylene-vinylacetate copolymer type resin resolved in methanol was used to laminate the said supporting member to both sides of the said multilayer film.
  • Amount of adhesive agent used here was 3.0 g/m2 terms of solid content.
  • Lamination was smooth in any case and there was no wrinkle, cut, or curling at time of drying which allowed homogeneous treatment.
  • the laminated body obtained is easy to handle, strong, while its layer M1 is protected from stain or cut and it was free from curling phenomenon after peeling.
  • This laminated body allowed easy peeling and was able to be used two stencil sheets.
  • tensile break strentgh was 178490 kPa (18.2 kg/mm2), tensile elongation at break 110 %, modulus of tensile elasticity 2158 mPa (220 kg/mm2), shrinkage stress value 42140 kPa (430g/mm2) (peak value at 85 °C ), thermal shrinkage ratio 78 % at 80 °C. All above results are average of vertical and horizontal direction and as well as results shown in later description.
  • Peeling between layer M1 and P B2- 1 was easy with its peeling force 0.784 Nm ⁇ 1 (0.8 g/cm) width which was appropriate.
  • the adhesive strength between layer P B2- 1 and layer P A- 1 was sufficient to allow no peeling.
  • the release agent provided a good bleedout over the interface with layer M1 and provided good peeling effect as well as appropriate adhesiveness between layer M1 and P B2- 1 to allow no break off of layers, wrinkle or float at all.
  • a test was done without release agent where layer M1 was torn and peeling was not smooth.
  • layers were subjected to dust, tearing, and wrinkle caused by spark.
  • Use of release agent not only permitted stable peeling effect between layers and other aforementioned effects but also stopped stick problem of line-type thermal head of printer (phenomenon where film sticks to thermal head, tears or sees wrinkles, causing distortion of art image which is formed by perforating).
  • the thickness of layer M1 was made at 0.5 »m and the same test was conducted to show almost the same property for film of said layer M1.
  • the compression ratio was 2.1 % on average of vertical and horizontal direction.
  • thickness of layer M1 was made at 10 »m and 12 »m, the film allowed homogeneous stretching and lamination compared with single M1 layer film. Homogeneous stretching was not possible due to puncture or extremely uneven thickness when thickness of single layer film was not more than 8 »m.
  • a non woven fabric made of polyester fiber with Metsuke 9.5 g/m2 was used with the film consisting of aforementioned functional layer (M1) which is 2 »m and 0.5 »m thick as supporting member, and was laid on both sides of aforementioned multilayer film with a methanol solution of ethylene-acetic acid vinyl copolymer type resin as an adhesive agent.
  • the amount of adhesive agent used was 3.5 g/m3 in terms of solid content.
  • both sides of this laminated member were peeled from the peeling layer portion (P B2- 1/P A- 1/ P B2- 1) at low tension of 1.96Nm ⁇ 1 (2 g/cm) width and at high speed of 200 m/min.
  • the peeling was made without difficulties and a desired stencil sheet was obtained.
  • the perforating sensitivity of the stencil sheet was measured to be at an ultra sensitive level of 0.03 mjoule for 0.5 »m thick M1, 0.04 mjoule for 1.0 »m thickness (the product obtained in the same way to possess all properties in the most favorable range, and the compression volume was 1.5 %).
  • the curling degree was also measured at an aging temperature of 40 °C and 50 °C to show 0 for all products at 40 °C and 0, 0, and 2 respectively for products of various thickness at 50°C.
  • the curling degree was measured when each of above layers M1 was peeled to be one separate film and laminated to non woven fabric (Metsuke 12.0 g/m2) made of aforementioned polyester type fiber without causing wrinkle.
  • the result was 8, 10 and 12 under aging at 40 °C and 25, 30, and 35 under aging at 50 °C while delamination phenomenon occurred when the stencil sheet using 1.0 »m and 2.0 »m, film was applied.
  • a stencil sheet was manufactured by using one sheet of crystalline polyethlene terephthalate film (crystallinity at density method;approx. 32 %) as the functional layer which was laminated with a supporting member similar to the aforementioned.
  • the perforating sensitivity of the stencil sheet was measured to be 0.12 mjoule for the one with 1.0 »m thickness and 0.13 mjoule for the one with 2.0 »m thickness.
  • the curling degree in this example was 8 for 40 °C aging and 16 for 50°C aging. From this result it can be concluded that a stencil sheet produced with a multilayer film of the present invention exhibits much higher perforating sensitivity and much better curling resistance after high temperature aging than the stencil sheet produced with commercial film.
  • Laminating film consisting of M1/P B2- 1/P A- 1/P B2- 1/M1 with respective thickness of 2/8/2/8/2 »m was manufactured in the same way as in example 1 except that resin consisting of layer M1 in the example 1 now includes 1 wt% of carbon black of which average particle diameter was 0.03 »m. All properties of this M layer film were in favorable range.
  • the stencil sheet consisting of M layer and supporting member was peeled off from original roll material which was obtained by laminating supporting member consisting of 200 mesh sheet to aforementioned multilayer film as was done in the example 1. Lamination was smooth and M layer of the stencil sheet had an even and flat face. The curling degree was 3 after 50 °C aging.
  • a polyethylene terephthalate film (thickness 2 »m) with a crystallinity of 45 % (by density method) and which includes 1 wt% carbon black with an average particle diameter of 0.03 »m was laminated as the supporting member to make a stencil sheet.
  • the perforating test was conducted, where in perforating was not possible at same amount of energy.
  • a multilayer film consisting of M1/P B2- 1/M1 with respective thicknesses of 2/15/2 (»m) was manufactured using the same films as used in example 1 for layer M and P B2- 1 under the same conditions except that the stretching temperature was set at 77°C, atmosphere temperature at 75 °C, stretching rate at vertically 4.0, horizontally 3.7 in addition to the one manufactured at same stretching temperature as example 1.
  • This example saw smooth stretching and no puncture or peeling phenomenon between layers occurred. All properties of M layer were in the most favorable range for this invention.
  • a multilayer product was obtained by using 8 openings/mm (200 mesh) sheet as supporting member and UV hardening agent as adhesive agent, and by laminating simultaneously the said supporting member to both sides of the said multilayer film.
  • Amount of hardening agent used was 0.4 g/m2.
  • Lamination was, smooth and a homogeneous original roll was obtained.
  • Compression volume of each multilayer film was measured to be -0.8 % (reducing) for the former and 1.5 % for the latter, and then perforating sensitivity of the stencil sheet for printing which was peeled off from multilayer product as was done in the example 1 was measured and proved to be ultra sensitive.
  • Curling degree was measured to be 14 and 2 (respectively) for 40 °C aging and 27 and 4 (respectively) for 50 °C aging.
  • the said supporting member was laminated with 2 »m thick crystal (crystallinity 45 % under density method) polyethylene phthalate film which was commercially available.
  • the product was subjected to wrinkle and lamination (possible only by applying stronger tension to vertical direction and horizontal direction) and the resulted film had inferior quality of wrinkles, uneven coating of adhesive agent, breaking and distortion.
  • concavity and convexity of the supporting member was copied to the surface of film and though the surface appeared to be more or less flat initially, curling degree was 8 after 24 hour aging at room temperature (23 °C), 12 for 40°C aging, and 15 for 50 °C aging.
  • Original roll was obtained by manufacturing a sheet shape pattern wherein there were convexities with 40 »m height and 20 »m diameter at 150 mesh intervals under resist method and thickness of the base part was 50 »m, using this pattern as a mount, laying and hardening multilayer film consisting of M1/P B1- 3/M1 (thickness 8/8/8 (»m)) obtained by the same method as in aforementioned example 3 after coating UV hardening agent to convex portion. Then a stencil sheet consisting of layer M1 and the mount was peeled off from above original roll and it was discovered that the surface of film possessed excellent evenness. Film property of layer M1 was in the most favorable range for the present invention.
  • Functional layer (M1), peeling layer (P B1- 1) and peeling layer (P B2- 1) are separately fused by extruder and though a ring shaped multilayer die the layers were extruded together to become multilayer tube shape with M1/P B2- 1/P B1- 1/P B2- 1/M1 structure before it was quenched to be hardened by refrigerant to obtain tube shape original roll.
  • This original roll was then heated to 105 °C and stretched simultaneously to two directions in bubble shape at speed of 50 m/min, and at 103°C heat so that the roll may be stretched 5.0 times vertically and 5.0 times horizontally before the product was cooled to 20°C to obtain 1100 mm folding width film folded by deflater.
  • the film was further submitted to heatset treatment under 75°C atomosphere for 5 seconds to be reduced by 3 % vertically and 5 % horizontally and then pressed by roll heated to 70°C for 0.5 second before two edges of the film were slit and rolled as two films. Accordingly multilayer film with thickness in order of 1.0/4/3/4/1.0 (»m) was obtained.
  • the multilayer film obtained by above-mentioned method possessed small peeling strength of 0.784Nm ⁇ 1 (0.8 g/cm) width between functional layer part (M1) and peeling layer part (P B2- 1) to allow easy peeling at 200 m/min speed. Compression rate of functional layer part after peeled as above was 1.2 % on average of vertical and horizontal direction.
  • Aforementioned functional layer part (M1) possessed tensile break strength 156910 kPa (16 kg/mm2), tensile elongation at break 100 %, elastic modulus in tenstion 2158 mPa (220 kg/mm2), shrinkage stress value at peak 4704 kPa (480 g/mm2) at 85 °C, 3430 kPa (350 g/mm2) at 100°C, thermal shrinkage ratio 5 % at 70 °C, 30 % at 80°C, 58 % at 90°C and 70 % at 100°C.
  • Peeling layer part possessed a thermal shrinkage ratio 15 % at 70°C, 43 % at 80°C, 71 % at 90°C and 76 % at 100°C. These values are all average of vertical and horizontal direction.
  • Multilayer film was manufactured in same conditions as in example 5 except that thickness of functional layer was made 0.5 »m, 2 »m or 6 »m. This example also permitted homogeneous laying of supporting member. Compression volume of functional layer peeled off from these multilayer films and curling degree of the stencil sheet made of these multilayer films are shown in table 1.
  • Co-stretching by bubble method in stretching condition same as example 1 followed by press roll treatment at 70°C for 0.5 sec. was applied to multilayer film (sample No. 1) consisting of M1/P B1- 2/M1 which was manufactured using functional layer (M1) and peeling layer (P B1- 2), multiayer film (sample No.2) consisting of M1/P B1- 2/P A- 2/P B1- 2/M1 which was manufactured using functional layer (M1), peeling layer (P B1- 2) and assisted peeling layer (P A- 2), multilayer film consisting of M2/P B2- 2/P A- 1/P B2- 2/M2 (sample No.3) which was manufactured using functional layer (M1), ethylene-vinylacetate copolymer (acetic acid vinyl unit content 10 wt%, melt index 1.0, Vicat softening point 81°C, fusion point 95 °C) containing 3 wt% mixture of 2 to 1 oleic acid monoglyceride and
  • stretching in the material No.3 was made with conditions where stretching temperature was set at 90 °C and atomosphere at 87 °C.
  • M2 showed tensile break strength 137300 kPa (14 kg/mm2), tensile elongation at break 70 %, modulus of tensile elasticity 2452 mPa (250 kg/mm2), peak of shrinkage stress value 5880 kPa (600 g/mm2) at 110 °C and 2550 kPa (260 g/mm2) at 100°C , and thermal shrinkage ratio 10 % at 80°C, 35 % at 100 °C and 55 % at 140 °C.
  • Stencil sheet was manufactured using above in the same way as example 1.
  • Table 3 shows compression volume of functional layer of these samples and curling degree and perforating sensitivity when original paper was manufactured.
  • Multilayer film (sample G) consisting of layer structure M1/PP/M1 and using only functional layer (M1) and crystalline polypropylene (shortened as PP) Used as content of P A- 1 as peeling agent, and multilayer film (sample H) consisting of layer structure M3/PP/M3 and using functional layer (M3) and above PP as peeling layer were manufactured in tha same way as in example 1. These had tendency to cause peeling between layers during stretching operation.
  • Table 4 shows test results on shrinkage rate (reverse of compression rate) as well as curling degree at time, of peeling of functional layer in the sample G and H.
  • crystal fusion energy of sample H was 33.5 J/g (8 cal/g) and based on this crystallinity (calculated using crystal fusion energy 125.6 J/g (30 cal/g) of crystal polyethylene terephthalate) was calculated to be about 26 %.
  • This film also exhibited heat shrinkage rate 7 % at 100°C, 20 % at 140 °C and 40 % at 160 °C.
  • Quenched original roll was heated to 80 °C before functional layer (M3) of sample H in comparative example 2, stretched by vertically 3.0 magnitude and by horizontally 3.0 in tenter of the following step at 90 °C, and multilayer film consisting of M3/PP/M3-1.0/5/1.0 (»m) was manufactured after the sample was heatset at 150 °C for 5 sec.
  • This multilayer film has cleavage in the tenter, the dislocation between film layers and the non-uniformity of thickness. And the separation of the functional layer and the peeling layer could't be made smoothly and the breakage was observed.
  • Curling degree was 5 vertically and 3 horizontally at 30 °C, 14 vertically and 8 horizontally at 40°C, and 25 ventically and 20 horizontally at 50 °C.
  • the perforating sensitivity of stencil sheet using this film was 0.10 mjoule.
  • the functional layer (M4), the peeling layer (P B1- 3) and the assisted peeling layer (P A- 1) were separately fused by extruder and through ring shape multilayer die the layer was extruded together to become multilayer tube shape with M4/P B1- 3/P A- 1/P B1- 3/M4 structure before it was quenched to be hardened by refrigerant to obtain tube shape original roll. Then the original roll was cooled by air of 20°C after the simultaneous biaxial stretching into a bubble shape at 100°C so that the roll may be stretched 3.0 times vertically and 3.0 times horizontally. Two edges of the film were slit and rolled up by rewinder as two films.
  • each layer in this laminating film was 1/8/2/8/1 (»m).
  • the peeling force between the functional layer part (M4) and the peeling layer part (P B1- 3) is as small as 0.98 Nm ⁇ 1 (1.0 g/cm) width in the multilayer film obtained in above-mentioned way, and the multilayer film was readily releasable.
  • the compressibility of the functional layer after peeling was 2.7 % on an average of length/width.
  • the thermal shrinkage rate at 100 °C of the layer (M4) was 43 % and the thermal shrinkage stress value of the layer (M4) was 4510 kPa (460 g/mm2). Both values are the avarage value of length/width.
  • the perforating sensitivity of the stencil sheet obtained by peeling of the peeling layer was high sensitivity level of 0.08 mjoule after laminating the non woven fabric of polyester fiber in the same way as example 1.
  • the curling degree of the stencil sheet obtained in this way was 0 at 30°C, 2 at 40 °C and 5 at 50 °C.
  • M4 layer was peeled to be a single layer for comparison the curling degree was respectively 8, 30, 40 and delamination phenomenon occurred.
  • the functional layer (M5), the peeling layer (P B1- 3) and tha peeling layer (P A- 1) were extruded through ring shape multilayer die to become tube shape with M5/P B1- 3/P A- 1/P B1- 3/M5 structure before it was quenched to be hardened by refrigerant to obtain tube shape original roll. Then the original roll was cooled by air at 20 °C after the simultaneous biaxial stretching in bubble shape at 90°C so that the roll may be stretched 3.0 times vertically and 3.0 times horizontally. Two edges of the film were slit and rolled up by rewinder as two films. The thickness of each layer in this laminating film was 1/6/2/6/1 (»m)
  • the peeling force between the functional layer (M5) and the peeling layer was as small as 1.0 g/cm width in the multilayer film obtaied in aforesaid way, and the multilayer film was readily releasable.
  • the shrinkage rate of the functional layer after peeling was 0.3 % on an average of length/width.
  • the shrinkage rate of the functional layer (M5) at 100°C was 63 % and the shrinkage stress at 70°C was 2060 kPa (210 g/mm2). Both values are the average value of length/width (crystallinity:14%).
  • the perforating sensitivity of the stencil sheet obtained by peeling of the peeling layer was high sensitivity level of 0.07 mjoule after laminating the non woven fabric of polyester fiber in the same way as example 1.
  • the curling degree of the stencil sheet obtained in this way was 0 at 30°C, 5 at 40 °C and 8 at 50 °C.
  • the original roll was cooled by air at 20°C after the simultaneous biaxial stretching in bubble shape at 130°C so that the roll may be stretched 1.5 times vertically and 1.5 times horizontally.
  • the thickness of each layer in the obtained laminating film (M1/P B2- 1/P A- 1/P B2- 1/M1) was 3/3/6/3/3/ »m.
  • the peeling force between the functional layer (M1) and the peeling layer in the obtained multilayer film was 5.39 Nm ⁇ 1 (5.5 g/cm) width and this multilayer film was a little bit hard to peel and was easy to be torn.
  • the shrinkage rate of the fanctional layer (M1) at 100 °C was 23 % and its balanced value was 28 % with the temperature of 110°C.
  • the shrinkage stress (equals to peak value) at 100 °C was 440 kPa (45 g/mm2). These values are the average of length/width.
  • Comparative example 5 was proceeded in the same way as example 1 except for the final thickness of the functional layer of 15 »m. Enough perforation could't be acquired even though the perforating sensitivity of the obtained stencil sheet was measured to be 0.13 mjoule.

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Claims (14)

  1. Hoch-wärmeempfindliche Mehrschichtfolie mit gemeinsam verstreckten Schichten, die mindestens zwei funktionelle Schichten (M) und mindestens eine Abschälschicht (P) umfaßt und eine Schichtkombination aufweist, in der mindestens eine ihrer äußersten Schichten eine funktionelle Schicht (M) ist, wobei die funktionellen Schichten einen Zugelastizitätsmodul von mindestens 196120 kPa haben und aus einer thermoplastischen Harzschicht bestehen, die eine Wärmeschrumpfungsrate von mindestens 30%, einen Wärmeschrumpfungs-Spannungswert im Bereich von 490 bis 11760 kPa (50 bis 1200 g/mm²), eine Kristallinität von nicht mehr als 30% und eine Dicke im Bereich von 0,1 bis 12 »m aufweist, wobei die an diese funktionelle Schicht angrenzende Abschälschicht einen Vicat-Erweichungspunkt im Bereich von 30 bis 120°C hat, mindestens ein Trennmittel enthält und aus einem thermoplastischen Harz besteht, das verschieden von dem der funktionellen Schicht ist, und diese beiden Schichten leicht abschälbar sind und die Abschälschicht (P) durch eine Kompressionsspannung im Bereich von 0,05 bis 10% in mindestens einer Richtung eine Kompressionskraft auf diese funktionelle Schicht (M) ausübt.
  2. Hoch-wärmeempfindliche Mehrschichtfolie nach Anspruch 1, wobei der die funktionelle Schicht (M) bildende Film die Wärmeschrumpfungsrate von mindestens 30% bei einer Temperatur im Bereich von 60 bis 170°C und den Wärmeschrumpfungs-Spannungswert von 490 bis 11760 kPa (50 bis 1200 g/mm²) bei einer Temperatur im Bereich von 60 bis 150°C aufweist.
  3. Hoch-wärmeempfindliche Mehrschichtfolie nach Anspruch 1, wobei die durch DSC bestimmte Kristallinität des Materials der Abschälschicht (P) nicht mehr als 60% der durchschnittlichen Kristallinität des diese Schicht bildenden gesamten Harzes beträgt.
  4. Hoch-wärmeempfindliche Mehrschichtfolie nach Anspruch 1, wobei die Anschälschicht (P) aus einer Mehrschicht-Abschälschicht besteht, die aus mindestens einer Hilfs-Anschälschicht (PA) und mindestens einer Trennmittel enthaltenden Haupt-Anschälschicht (PB) gebildet ist und die Hilfs-Abschälschicht aus einem thermoplastischen Harz gebildet ist, das einen Kristallschmelzpunkt, der hoher ist als die Verstreckungstemperatur der funktionellen Schicht, und einen Vicat-Erweichungspunkt von mehr als 120°C hat.
  5. Hoch-wärmeempfindliche Mehrschichtfolie nach Anspruch 1 oder Anspruch 3, wobei die Anschälschicht (P) aus mindestens einer Hilfs-Anschälschicht (PA) und mindestens einer Trennmittel enthaltenden Haupt-Abschälschicht (PB), die an eine der Oberflächen der Hilfs-Abschälschicht (PA) angrenzt und leicht von der Funktionsschicht (M) abschälbar ist, besteht und wobei diese Abschälschichten so übereinander gelagert sind, daß eine Trennung zwischen PB und PA überhaupt nicht oder nur unter einer Abschälkraft eintritt, die größer ist als die für die Trennung zwischen M und PB.
  6. Hoch-wärmeempfindliche Mehrschichtfolie nach Ansprüchen 1, 2 und 5, wobei die funktionellen Schichten auf beide Oberflächenschichten der Mehrschichtfolie laminiert sind.
  7. Hoch-wärmeempfindliche Mehrschichtfolie nach Anspruch 1, wobei die funktionelle Schicht (M) hauptsächlich aus mindestens einem Harz gebildet ist, das unter Copolymeren vom Polyestertyp, Copolymeren vom Nylontyp, Copolymeren vom Polycarbonattyp und Copolymeren vom Ethylen-Vinylalkohol-Typ ausgewählt ist, die jeweils in Form der Folie eine im wesentlichen amorphe Textur annehmen und einen Vicat-Erweichungspunkt im Bereich von 40 bis 150°C aufweisen.
  8. Verfahren zur Herstellung einer hoch-wärmeempfindlichen Schablonenplatte aus einer Mehrschichtfolie mit gemeinsam verstreckten Schichten nach einem der vorhergehenden Patentansprüche, das dadurch gekennzeichnet ist, daß ein poröses Trägerteil (S) auf mindestens eine der funktionellen Schichten aufgelegt wird und danach die Mehrschichtfolie an der Grenzfläche zwischen der funktionellen Schicht (M) und der Anschälschicht (P) getrennt wird, wobei die funktionelle Schicht (M) von der Kompressionskraft befreit wird, die durch die Anschälschicht (P) ausgeübt wird, und wobei die Beständigkeit der Schablonenplatte gegen Wellenbildung erhöht wird.
  9. Verfahren nach Anspruch 8, wobei die funktionellen Schichten auf beide Oberflächenschichten der Mehrschlchtfolie auflaminiert sind.
  10. Verfahren nach Anspruch 8 oder Anspruch 9, wobei die Anschälschicht (P) aus einer mehrschichtigen Anschälschicht besteht, die aus einer Hilfs-Anschälschicht (PA) und einer auf einer Oberfläche der Hilfs-Abschälschicht (PA) angeordneten Trennmittel enthaltenden Haupt-Anschälschicht (PB) gebildet ist und die Hilfs-Abschälschicht (PA) aus einem thermoplastischen Harz gebildet ist, das eine Kristallisationstemperatur höher als die Verstreckungstemperatur der funktionellen Schicht und einen Vicat-Erweichungspunkt von mehr als 120°C aufweist.
  11. Verfahren nach Anspruch 8, wobei die funktionelle Schicht (M) hauptsächlich aus mindestens einem Harz gebildet ist, das unter Copolymeren des Polyestertyps, Copolymeren des Nylontyps, Copolymeren des Polycarbonattyps und Copolymeren des Ethylen-Vinylalkohol-Typs ausgewählt ist, die jeweils eine im wesentlichen amorphe Textur in der Form einer Folie annehmen und einen Vicat-Erweichungspunkt im Bereich von 40°C bis 150°C besitzen.
  12. Laminat, in dem ein poröses Trägerteil (S) auf mindestens zwei funktionellen Schichten (M) in einer Mehrschichtfolie mit gemeinsam verstreckten Schichten angeordnet ist, die mindestens eine funktionelle Schicht (M) und mindestens eine Abschälschicht (P) aufweist und eine Schichtenkombination hat, in der mindestens eine ihrer äußersten Schichten eine funktionelle Schicht (M) ist, wobei die funktionelle Schicht aus einer thermoplastischen Harzschicht besteht, die eine Wärmeschrumpfungsrate von mindestens 30%, einen Wärmeschrumpfungs-Spannungswert im Bereich von 490 bis 11760 kPa (50 bis 1200 g/mm²), eine Kristallinität von nicht mehr als 30% und eine Dicke im Bereich von 0,1 bis 12 »m hat und die an die funktionelle Schicht angrenzende Abschälschicht einen Vicat-Erweichungspunkt im Bereich von 30 bis 120°C hat, ein Trennmittel enthält und aus einem thermoplastischen Harz besteht, das verschieden von dem der funktionellen Schicht ist, wobei die zwei Schichten leicht voneinander abschälbar sind, die Anschälschicht (P) durch eine Kompressionsspannung im Bereich von 0,05 bis 10% in mindestens einer Richtung eine Kompressionskraft auf die funktionelle Schicht (M) ausübt.
  13. Laminat nach Anspruch 12, wobei die funktionellen Schichten auf beide Oberflächenschichten der Mehrschichtfolie laminiert sind.
  14. Laminat nach Anspruch 12 oder Anspruch 13, wobei die funktionelle Schicht (M) hauptsächlich aus mindestens einem Harz gebildet ist, das unter Copolymeren des Polyestertyps, Copolymeren des Nylontyps, Copolymeren des Polycarbonattyps und Copolymeren des Ethylen-Vinylalkohol-Typs ausgewählt ist, die jeweils in Form der Folie eine im wesentlichen amorphe Textur annehmen und einen Vicat-Erweichungspunkt im Bereich von 40 bis 150°C besitzen.
EP19890307285 1989-01-12 1989-07-19 Höchst wärmeempfindlicher Mehrschichtfilm und Herstellungsverfahren für eine Schablone Expired - Lifetime EP0377935B1 (de)

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US5888653A (en) * 1993-11-17 1999-03-30 Toray Industries, Inc. Heat-sensitive mimeograph stencil
FI104887B (fi) * 1994-06-16 2000-04-28 Enso Gutzeit Oy Tuotepakkauksen kansi ja menetelmä sen valmistamiseksi
JPH08175045A (ja) * 1994-12-21 1996-07-09 Riso Kagaku Corp 孔版印刷用原紙
JP3621425B2 (ja) * 1996-06-24 2005-02-16 イーストマン ケミカル カンパニー 収縮フィルム用可塑化ポリエステル
DE29814711U1 (de) * 1998-08-17 1998-10-22 Haverkamp SST Sicherheitstechnik GmbH, 48165 Münster Mehrschichtige Schutzfolie und Flächenelement mit verschleißgeschützter Oberfläche
CN1122636C (zh) * 2001-03-19 2003-10-01 李洪岭 一种从硼泥中回收硼酸的方法
JP4734764B2 (ja) * 2001-05-29 2011-07-27 アイシン精機株式会社 自動車用モール及びその製造方法
CN109304955B (zh) * 2017-07-26 2020-05-12 大勤化成股份有限公司 转印膜结构及其制法与立体转印品及其制法
EP3677434B1 (de) * 2017-08-31 2022-10-19 FUJIFILM Corporation Lithografische originaldruckplatte und verfahren zur herstellung einer lithografischen druckplatte
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EP0377935A3 (de) 1991-07-17
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