WO1999009102A1 - Resin composition for cards, and sheets and cards - Google Patents
Resin composition for cards, and sheets and cards Download PDFInfo
- Publication number
- WO1999009102A1 WO1999009102A1 PCT/JP1998/002545 JP9802545W WO9909102A1 WO 1999009102 A1 WO1999009102 A1 WO 1999009102A1 JP 9802545 W JP9802545 W JP 9802545W WO 9909102 A1 WO9909102 A1 WO 9909102A1
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- Prior art keywords
- card
- weight
- resin composition
- crystalline polyester
- resin
- Prior art date
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Classifications
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/04—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the shape
- G06K19/041—Constructional details
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/02—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the selection of materials, e.g. to avoid wear during transport through the machine
Definitions
- the present invention relates to a resin composition used for a material of a plastic card such as a magnetic stripe card and an IC card, and a sheet and a card produced on the card.
- plastic cards such as magnetic stripe cards and IC cards
- polychlorinated vinyl resin (hereinafter referred to as “PVC”) has been used.
- PVC polychlorinated vinyl resin
- magnetic stripe cards are made by laminating transparent oversheets with magnetic stripes above and below a white core sheet, bonding the layers together by hot pressing (hereinafter referred to as “lamination”), and then punching out the blade. It is manufactured by cutting into a card shape with a stamping machine and finally embossing with a stamping machine.
- the sheet is pre-applied with the printing power S required for the front card.
- PVC is suitable as a plastic card material because it can be mass-produced by calendering and has excellent secondary workability such as lamination suitability, peelability from the press plate after lamination, and embossing stamping. Material.
- polyester-based materials that are non-PVC-based card materials include, for example, substantially those in which the monomer component before polymerization is terephthalic acid and the diol components are ethylene glycol and cyclohexanedimethanol.
- non-crystalline polyester resins Compared to PVC, non-crystalline polyester resin has excellent laminating properties at low temperatures, good engraving properties, and excellent durability against repeated bending and twisting when it is made into a card. is there.
- non-crystalline polyester resins are still insufficient in terms of force secondary processing, which is attracting attention as a suitable card material. That is, when a card made of only an amorphous polyester resin is exposed to a high temperature, the card may be warped or embossed. Furthermore, when the punching into a card shape, greater elongation of the over sheet of male and female clearance blade Nuku out is flat punching member forces? Obtained Nikure. If the card was curled or if the cut surface of the card was not flat, not only the touch was poor, but also the cross section could be caught by the machine when inserting or removing the card from the card reader.
- non-PVC-based non-crystalline polyester resin with excellent environmental suitability is not enough in terms of the force s that is suitable for card base material s, and the secondary workability.
- improvements have been desired to satisfy the required secondary workability. Disclosure of the invention
- the present invention has been made to solve the above problems, and an object of the present invention is to provide a resin composition for a plastic card, a sheet, and a card made of a non-pVC resin which do not generate card warpage or emboss curl. To provide. Another object of the present invention is to provide a resin composition, a sheet and a card for a non-PVC-based resin, which has a flat punched-out cross section of the card. Still another object of the present invention is to provide a resin composition for non-PVC-based plastic forceps, a sheet and a card, which have improved releasability from a press plate.
- a first aspect of the resin composition for a card of the present invention is characterized by containing a substantially non-crystalline polyester-based resin as a main component.
- the second embodiment of the resin composition for a card of the present invention is used for a plastic card material.
- a third embodiment of the resin composition for a card according to the present invention is directed to a substantially non-crystalline polyester-based resin, wherein at least one of a powdered caic acid and a powdered magnesium silicate having an average particle size of 5 ⁇ m or less is used. Is contained in the range of 0.5 to 5.0% by weight with respect to the substantially non-crystalline polyester resin.
- a fourth aspect of the card resin composition of the present invention the substantially non-crystalline polyester Le resins, particulate having an average particle size of. 3 to 1 0 mu m and / or plate-like inorganic FILLER one
- the content is in the range of 2 to 10% by weight based on the substantially non-crystalline polyester resin.
- the resin composition for a card may be a polyester resin obtained by dehydrating and condensing a mixture of terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol from a non-crystalline polyester resin.
- the sheet of the present invention is characterized by being produced using any one of the resin compositions for cards.
- the card of the present invention is characterized by having a layer produced using any one of the above resin compositions for cards.
- the resin composition for a card is composed of a substantially non-crystalline polyester resin and polyethylene glycol and sodium alkylbenzene sulfonate in a weight ratio.
- Another aspect of the card of the present invention is a card having an oversheet as an outermost layer and a core sheet as an inner layer, wherein the core sheet is substantially made of an amorphous polyester-based resin, and the oversheet is made of glass. It is characterized by comprising a resin composition having a transition temperature of 90 to 140 ° C.
- the oversheet can be made of polycarbonate resin.
- the non-crystalline polyester resin may be a polyester resin obtained by dehydration-condensing a mixture of terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol.
- the resin composition of the present invention contains a substantially non-crystalline polyester resin as a main component.
- the polyester as used herein refers to a dehydrated condensate of a dicarboxylic acid and a diol.
- the “substantially non-crystalline polyester” used in the present invention refers to an acid component or a diol component of a monomer before polymerization. Alternatively, it is a transparent copolyester resin in which both the acid component and the diol component are composed of two or more components. What does not happen.
- terephthalic acid as the dicarboxylic acid, isophthalic acid, adipic acid, naphthalene dicarboxylic acid, and examples of the diol ethylene glycol, diethylene glycol, triethylene glycol, force s like Kisanjimeta Nord cyclohexylene.
- the combination of an acid component and a diol component is appropriately performed.
- the selection is appropriately performed.
- a polyester resin in which the acid component of the monomer before polymerization is terephthalic acid and the diol components are ethylene glycol and cyclohexane dimethanol (trade names: PETG, Eastman Chemical Co., Ltd.) is commercially available.
- an additive such as a coloring agent may be added.
- the polyethylene glycol to be added to the substantially non-crystalline polyester resin is not particularly limited, but a solid wax having a molecular weight of 1,000 to 500,000 can be easily mixed with the pellet, and a sheet. It is preferably used because it is difficult to volatilize due to the heat required when processing into steel.
- the sodium alkylbenzenesulfonate used here is not particularly limited in terms of the length of the alkyl group, but sodium laurylbenzenesulfonate is easily available commercially and can be suitably used.
- the ratio of polyethylene glycol to sodium alkylbenzene sulfonate added to the substantially non-crystalline polyester resin is preferably in the range of 1Z9 to 9/1 by weight.
- Polyethylene glycol and alkylbenzene sulfo added When the ratio of sodium phosphate is out of the above range, the peelability from the press plate after lamination is sufficient.
- a plastic card such as a magnetic stripe card or an IC card is formed by laminating a plurality of sheets, and the outermost layer is called an over-sheet and the inner layer is called a core sheet.
- the sheet size of the core layer and the overlayer to be laminated differs depending on the card manufacturer, and the overlayer may be slightly smaller than the core layer. Therefore, it is necessary to improve not only the releasability of the overlayer but also the core layer from the press plate.
- the added amount of polyethylene glycol and sodium alkyl benzene sulfonate is in the range of 0.1% by weight to 1.5% by weight based on 100% by weight of the amorphous polyester resin. It is preferably from 0.2% to 1.5% by weight, more preferably from 0.5% to 1.0% by weight.
- the sheet has excellent physical properties and printability.
- the printability means the familiarity between the ink used when printing on a sheet and the sheet. If the printability is poor, ink repelling may occur, making it impossible to print cleanly on the sheet.
- the resin composition is also excellent in antistatic properties, has the advantage that the sheet is not easily fed during printing due to static electricity, does not cause jumps, and has the advantage that sparks are less likely to occur during press work.
- a powdery keic acid having an average particle diameter of 5 ⁇ m or less and Z or a powdery magnesium silicate are added to a substantially non-crystalline polyester resin, and the polyester resin is added in an amount of 100% by weight. 0/0 5 against 5. by 0 weight 0/0 by containing, secured the transparency of the card, the force one de made does not occur cracking force of engraved portions, and flat punching member forces s obtained.
- Powdered caustic acid is transparent but hard, whereas powdered magnesium silicate is soft but has reduced transparency. Therefore, it may be appropriately selected according to the characteristics required for the sheet or the card.
- powdery The acid and the powdery magnesium silicate may be used alone, but may be used in combination. Therefore, the combination ratio and the like may be appropriately selected according to the properties required for the card and the like.
- the content with respect to the polyester resin is 0.5 to 5.0% by weight.
- the amount of the powdered caic acid is 0.5% by weight or more, the effect of improving the punched cross section can be obtained. Although the transparency does not decrease even if the amount of the powdered kaic acid exceeds 5.0% by weight, the hardness becomes hard, so that the abrasion of the punching blade and the cracking of the engraved portion are liable to occur. If the amount of the powdered magnesium silicate is 0.5% by weight or more, the effect of improving the punched cross section can be obtained. On the other hand, if the amount of the powdered magnesium silicate exceeds 5.0% by weight, abrasion of the punching blade and cracking of the stamped portion do not occur, but the transparency of the sheet is reduced.
- the powdery kaic acid and the powdery magnesium silicate used here have an average particle size of 5 ⁇ m or less. If powdered citric acid having an average particle size of more than 5 m is used, the punching blade force is easily worn when punching into a card shape, and the impact resistance of the sheet is reduced. This is because the stamp may be broken. Also, if powdered magnesium silicate having an average particle size of more than 5 m is used, transparency is reduced, and visibility of a pattern or a character may be reduced.
- plastic cards such as magnetic stripe cards and IC cards are formed by laminating a plurality of sheets, and the outermost layer is called an oversheet and the inner layer is called a core sheet.
- the card produced is intended to have a flat stamped cross-section, at least one of the core sheet and the oversheet contains such a powdered kaic acid and / or a powdered magnesium silicate.
- an overseat it is preferable to use an overseat for the following reasons. That is, usually, core sheet requires hiding property, and to be a base of the print layer or the print layer is required, which is titanium oxide power? Added. For this reason, it is unlikely that the core sheet will greatly expand due to the clearance between the male and female dies in the punching process. Therefore, it is preferably used for paper sheets with poor punching performance.
- a granular and / or plate-like inorganic filler having an average particle diameter of 3 to 10 m is added to the substantially non-crystalline polyester resin by adding 100% by weight of the non-crystalline polyester resin. by containing 2-1 0% by weight relative to the 0/0, it is possible to improve the embossing force one le of the card to be manufactured.
- the type of the inorganic filler used here is not particularly limited as long as its shape is granular or plate-like and the average particle is 3 to 10 z ⁇ m. Specific examples include talc, magnesium silicate, calcium carbonate, silica, myriki, or a mixture thereof. That is, needle-like materials such as glass fibers are not included.
- the average particle size of the inorganic filler is 3 m or more, the effect of preventing the occurrence of emboss curl is great, and when the average particle size is 10 m or less, the impact resistance of the obtained sheet is sufficient. Does not break.
- the amount of the inorganic filler added to the non-crystalline polyester resin is in the range of 2 to 10% by weight, the effect of improving the embossing force is large, and the problem of cracking of the engraved portion does not occur.
- At least one of them may be made of such a resin containing an inorganic filler, but the core sheet may be used for the following reasons. preferable.
- the core sheet is usually printed with personal information and the like, and is protected by an oversheet.
- Oversheets are used to protect the print of the core sheet and to decorate the print, and are often thin and transparent.
- the card is required to have an appropriate thickness and high light concealment and reflection properties due to the characteristics of the reader / writer, so the core sheet is thick and contains a coloring agent such as titanium oxide.
- the embossing process is performed after laminating the upper sheet and the core sheet, if the purpose is to improve the emboss curl, at least one of the core sheet and the over sheet is made of such a resin containing an inorganic filler. Any sheet may be used. However, as described above, usually, the core sheet is preferably used for the core sheet because the core sheet is thicker than the over sheet and the over sheet has transparency.
- the resin composition described above can be used to form a sheet by a known method such as, for example, a melt extrusion method, or a magnetic stripe card or a plastic card such as an IC card. Can also. Note that an antistatic agent or the like may be added to the core sheet.
- the core sheet is made of a substantially non-crystalline polyester resin
- the oversheet is made of a resin having a glass transition temperature of 90 to 140 ° C., whereby the heat resistance temperature of the card is improved. Can be raised.
- Such a core sheet is obtained by adding an additive, for example, a coloring agent such as titanium oxide, a slipping agent, an antistatic agent, etc. to a substantially non-crystalline polyester resin, and applying a melt extrusion method or the like. Therefore, it can be obtained.
- an additive for example, a coloring agent such as titanium oxide, a slipping agent, an antistatic agent, etc.
- the glass transition temperature of the oversheet is 90 ° C or more, the heat resistance of the card is sufficiently improved, and if it is 140 ° C or less, sufficient adhesion to the core sheet can be obtained during lamination. Thus, there is no need to raise the temperature to improve the fusibility, so the co-sheet does not flow and does not become thinner than the desired card thickness.
- the glass transition temperature is determined from the peak of the loss modulus in the measurement of dynamic viscoelasticity at a frequency of 1 Hz. Specifically, the temperature dependence of the tensile modulus is measured using a viscoelastic spectrometer while applying a sinusoidally changing strain at a frequency of 1 Hz to the sample.
- the measurement conditions were as follows: the sample thickness was 1 mm, the maximum strain was 1%, the heating rate was 4 ° CZ min., Starting from room temperature, the tensile loss modulus E "showed a peak at the maximum force s , and the tensile storage modulus E 'was large. The temperature near the beginning of the decrease was defined as the glass transition temperature.
- a polycarbonate (hereinafter sometimes abbreviated as “PC”) resin is cited because it can be heat-fused with an amorphous polyester resin.
- PC polycarbonate
- copolymerized PC obtained by copolymerizing an aliphatic dicarboxylic acid, one obtained by adding a plasticizer to PC and adjusting the glass transition temperature to fall within the above range, and the like can also be used.
- a slipping agent, an antistatic agent, and the like may be added to these resins.
- the sheet can be obtained by a known method such as a melt extrusion method.
- PETG 667 manufactured by Yeastman Chemical Company
- titanium oxide as a white pigment
- polyethylene glycol molecular weight 3
- a sheet having a thickness of 400 / m was obtained by a T-die extrusion method using a mixture of (0000)) and sodium laurylbenzenesulfonate or another slip agent as shown in Table 1.
- the obtained sheet was pressed to a size of 200 mm ⁇ 200 mm, and two cut sheets were stacked and sandwiched between two chromium-plated steel sheets, and the pressing temperature was set at 120 ° C.
- the sample pressure was kept at 50 kgf Z cm 2 for 10 minutes. Then bring this to room temperature After cooling, the chrome plated steel sheet was taken out and the two chrome plated steel sheets were peeled off. The force required to peel off the chrome plated steel plate was evaluated by tactile sensation, and the peelability from the plated plate was evaluated.
- the surface tension of the obtained extruded sheet was measured using a wet index standard solution (manufactured by Nacalai Tesque).
- the evaluation criteria were as follows: Regarding the "peelability from the plating plate" in the table, “A” indicates that it can be easily peeled, and “B” indicates that it exhibits peelability with resistance but practical. Those that could not be evaluated were designated as “C.”
- the “Printability” was rated “A” for those with a surface tension of 38 dyne / cm or more, and “B” for those with a surface tension of 36 dyn eZcm or more and less than 38 dyne eZcm. And less than 36 dyne / cm were designated as “C”.
- the addition amount of the lubricant in the table is the Weight 0/0 when the PETG 6 763 1 00 and, PEG is an abbreviation for polyethylene glycol, LB S in abbreviation Natoriumu laurylbenzenesulfonate is there.
- Example 1-1 A sample for evaluation was prepared in the same manner as in Example 1-1 except that the type and amount of the slipping agent in Example I-11 were changed as shown in Tables 1 to 3.
- Example I-1 I-15 and Control I_1 I_8 the card having the structure of the present invention was found to be excellent in peelability and printability.
- the same result is obtained with a force obtained by laminating two sheets of substantially non-crystalline polyester resin containing a white pigment, and a force obtained by forming a core layer and an over layer. Obtainable.
- Example II-1 the same applies to other configurations.
- T-die extrusion of non-crystalline polyester obtained by adding titanium oxide to PE TG 6763 (manufactured by Istman Chemical Co., Ltd.) to a concentration of 10% by weight.
- PE TG 6763 manufactured by Istman Chemical Co., Ltd.
- a core sheet having a thickness of 560 m was obtained by the coating method.
- PETG6763 0.5 weight 0/0 to 100 weight 0/0 lauryl base sodium Nze Nsuruhon acid PETG6763 as a crystalline polyester, polyethylene glycol of molecular weight 3000 to those obtained by adding 0.5 wt%, average particle size as an additive 0.6% by weight of 3 m of citric acid was mixed, and an oversheet having a thickness of 100 m was obtained by a T-die extrusion method.
- the amounts of the additives shown in the table are% by weight with PETG 6763 being 100.
- a pattern is printed on both sides of the obtained core sheet by the silk screen printing method, oversheets are overlaid on both sides, sandwiched between two chrome plated steel sheets, and pressed at a temperature of 120 ° (:, sample pressure of 20 kgf Zcm 2 at 5 kgf Zcm 2) . After holding for 1 minute, it was cooled to room temperature, taken out of the chrome plating plate, and punched into a card shape with a punching blade composed of a male die and a female die, with a clearance of 30 m between the male die and the female die.
- the obtained card sample for evaluation was embossed by the following method using an electric enbosser, the foil of the engraved portion was transferred by a chipper, and the evaluation was performed according to the following criteria.
- the average particle size was determined as follows.
- the mode diameter was determined from the particle size distribution data measured by a sedimentation type particle size distribution analyzer S A—CP 2-20 (manufactured by Shimadzu Corporation), and the average particle size was determined.
- Example II—2 to ⁇ —5 Control II—1-111 to 9
- Example II-1 a card sample for evaluation was prepared in the same manner as in Example II-11 except that the types and amounts of additives added to the oversheet were changed as shown in Table 4. The same evaluation as in 1 was performed.
- the unit of the additive amount is% by weight ( As is evident from Table 4, a card using a resin containing caic acid with an average particle size of 5 or less and Z or magnesium silicate as an over-sheet produces a character breaking force of 5 'at the IJ mark. It was a transparent card with excellent transparency and a punched cross section.
- Respect PETG 6 7 (manufactured by Eastman Chemical Company) 6 3 1 0 0 part by weight as a non-crystalline polyester, 0 sodium lauryl benzene sulfonate. 5 wt 0/0, the molecular weight 3 0 0 0 polyethylene glycol 0. 5% by weight was added, and an oversheet having a thickness of 100 // m was obtained by a T-die extrusion method.
- a pattern is printed on both sides of the obtained core sheet, the oversheet is overlaid on both sides, sandwiched between two chrome-plated steel sheets, and kept at a press temperature of 120 ° C and a sample pressure of 20 kgf / cm2 for 5 minutes. After cooling to room temperature, it was taken out of the chrome plating plate and punched into a card shape with a punching blade composed of a male die and a female die to produce a card sample for evaluation.
- the obtained card sample for evaluation was embossed as described in Example II-11 using an electric enbosser, the foil at the engraved portion was transferred using a chipper, and evaluated according to the following evaluation criteria.
- the average particle size of the inorganic filler was determined as follows.
- the mode diameter was determined from the particle size distribution data measured by a sedimentation type particle size distribution analyzer S A—C P 2—20 (manufactured by Shimadzu Corporation), and the average particle size was determined.
- Example III-11 a card sample for evaluation was prepared in the same manner as in Example III-1, except that the type and amount of the inorganic filler added to the core sheet were changed as shown in Table 5. The same evaluation as in 1 was performed.
- PETG (Eastman) is a non-crystalline polyester containing terephthalic acid as the acid component and ethylene glycol (about 70 mol%) and cyclohexanedimethanol (about 30 mol 0 / o) as the diol component. 100 parts by weight of Titanium Co., Ltd. was added to 100 parts by weight of Titanium Co., Ltd., and a white core sheet having a thickness of 300 / m was obtained by a T-die extrusion method.
- a transparent oversheet having a thickness of 100 was obtained by a T-die extrusion method using Lexan SP101 (manufactured by Nihon Giplastic Co.), which is a copolymerized polycarbonate.
- the glass transition temperature of the over sheet is 130 ° C. However, the glass transition temperature was measured as follows.
- the temperature dependence of the tensile modulus was measured while applying a sinusoidally changing strain at a frequency of 1 Hz to the sample.
- the measurement conditions were: sample thickness lmm, maximum strain 1%, heating rate 4 ° C / min, and started at room temperature.
- the temperature near the point where the tensile loss elastic modulus E "shows a maximum peak and the tensile storage elastic modulus E, starts to decrease significantly is defined as the glass transition temperature.
- a loop coil for a four-turn antenna in which a copper wire having a wire diameter of 0.15 mm is wound around the obtained core sheet four times, and an IC chip having a size of 5 mm X 5 mm and a thickness of 0.35 mm, etc. Were arranged at equal intervals, temporarily fixed with a cyanoacrylate-based instant adhesive, and a core sheet was stacked so as to sandwich an IC chip and the like.
- Example IV-1 the oversheet was added to 100 parts by weight of Novalex polycarbonate (manufactured by Mitsubishi Engineering-Plastics Corporation) 100 parts by weight with plasticizer TCP (tricresyl phosphate, A card sample for evaluation was prepared in the same manner as in Example IV-1, except that an oversheet consisting of a mixture to which 5 parts by weight of Daihachi Chemical Co., Ltd.) was added was used.
- the glass transition temperature of the oversheet is 135 ° C Met.
- Example IV-2 an evaluation force sample was prepared in the same manner as in Example IV-2, except that the amount of the plasticizer TCP used for the oversheet was changed to 18 parts by weight.
- the glass transition temperature of the oversheet was 90 ° C.
- Example IV-1 An evaluation card sample was prepared in the same manner as in Example IV-1, except that in Example IV-1, the oversheet was replaced with an oversheet made of NOVAREX 720-2.
- the glass transition temperature of the oversheet was 155 ° C. Control IV—2
- Example IV-2 an evaluation force sample was prepared in the same manner as in Example IV-2, except that the amount of the plasticizer TCP used for the oversheet was changed to 25 parts by weight.
- the glass transition temperature of the oversheet was 80 ° C.
- Examples IV—1 to IV—3, Control IV—1 to! The following evaluation was performed on the evaluation card sample obtained in V-2.
- the “warpage” generated in the evaluation card sample was measured as follows. Place the evaluation card sample in an oven at a predetermined temperature, leave it for 24 hours, remove it, place the evaluation card sample cooled to room temperature on a horizontal plate, and set the maximum distance from the horizontal plate to the evaluation card sample surface ( (Including the thickness of the card sample). The set temperature of the oven was increased every 50 ° C from 50 ° C, and the maximum temperature at which the measured value did not exceed 2 mm was defined as the “heat-resistant temperature”.
- evaluation card sample was immersed in liquid paraffin at 150 ° C. for 5 minutes, it was taken out and the cross section of the peripheral portion of the evaluation card sample was visually observed.
- the heat resistance temperature of Examples IV-1 and IV-2 whose glass transition temperature is 90 ° C or more is 80 ° C, and that of Example IV-3 is 70 °, both of which are 70 ° C.
- the heat resistance temperature of Control IV-2 which is not less than C but has a glass transition temperature of less than 90 ° C, was 60. That is, the heat resistance temperature of Examples IV-1 to IV-3 is higher than the practical level, while that of Control IV-2 is lower than the practical level.
- Embodiment IV-1! V-3 obtained excellent results in both the card peeling test and the heat resistance test.
- Example IV-1 100 parts by weight of titanium oxide, 0.5 parts by weight of sodium ruralylbenzenesulfonate, and 100 parts by weight of the amorphous polyester (PETG6673) were used as the core sheet. After the addition of 0.5 parts by weight of polyethylene glycol having a molecular weight of about 300, and lamination using an oversheet having a size slightly smaller than the core sheet, the same procedure as in Example IV-1 was repeated. Got a sample.
- the powdered Ca-acid and Z or powdered magnesium silicate having an average particle size of 5 ⁇ 111 or less were added to the substantially non-crystalline polyester resin with respect to 100% by weight of the non-crystalline polyester resin.
- the resin composition containing 0.5 to 5.0% by weight has excellent transparency, does not cause character cracks in the engraved portion of the card, has a flat punched cross section, has a good feel, and has a good card reader. The cross section does not catch on the machine when moving in and out.
- the resin composition containing 0.5 to 5.0% by weight of the inorganic polyester resin of dog with respect to 100% by weight of the non-crystalline polyester resin has a small embossed curl without character breakage at the engraved portion. Therefore, the card does not catch on the machine when inserting or removing the card from the reader / writer.
- the core sheet is a sheet made of an amorphous polyester resin
- the oversheet is a plastic card made of a sheet with a glass transition temperature of 90 to 140 ° C. And solve card warpage.
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Abstract
Plastics are improved in secondary processabilities so as, e.g., not to suffer curling by embossing, not to suffer card warpage upon exposure to high temperatures, to give flat sections upon card formation by punching, and to have satisfactory releasability from the press plates. According to the properties required, various means are taken to modify substantially noncrystalline polyester resins. For example, a mixture of polyethylene glycol with a sodium alkylbenzenesulfonate in a weight ratio of from 1/9 to 9/1 is added to the resin in an amount of 0.2 to 1.5 % by weight. Alternatively, powdery silicic acid and/or powdery magnesium silicate each having an average particle diameter of 5 νm or smaller is incorporated in an amount of 0.5 to 5.0 % by weight, or a particulate and/or flaky inorganic filler having an average particle diameter of 3 to 10 νm is incorporated.
Description
明細書 Specification
力一ド用樹脂組成物、 シートおよびカード Resin composition, sheet and card for forceps
技術分野 Technical field
本発明は、 磁気ストライプカード、 I Cカードなどのプラスチックカードの素 材に用いられる樹脂組成物、 カードに作製されるシートおよびカードに関するも のである。 背景技術 The present invention relates to a resin composition used for a material of a plastic card such as a magnetic stripe card and an IC card, and a sheet and a card produced on the card. Background art
磁気ストライプカードや I Cカードなどのプラスチックカードの素材として は、 従来よりポリ塩ィ匕ビニル系樹脂 (以下 「P V C」 という) が使われている。 磁気ストライプカードは、 一般に、 白色系のコアシートの上下に磁気ストライ プを設けた透明系のオーバーシートを重ねて熱プレスで層間を接着 (以下 「ラミ ネート」 という) した後、 これを打ち抜き刃でカード形状に切断し、 最後に刻印 機でエンボス刻印を行うことにより製造される。 As a material for plastic cards such as magnetic stripe cards and IC cards, polychlorinated vinyl resin (hereinafter referred to as “PVC”) has been used. In general, magnetic stripe cards are made by laminating transparent oversheets with magnetic stripes above and below a white core sheet, bonding the layers together by hot pressing (hereinafter referred to as “lamination”), and then punching out the blade. It is manufactured by cutting into a card shape with a stamping machine and finally embossing with a stamping machine.
I Cカードは種々の方法により製造される力 ?、 磁気ストライプカードの製造と 同様に、 2種類のシートを接着してカード素材を作製し、 後加工で I Cチップを 装着する凹み部を切削加工する方式が主流になりつつある。 Power IC card produced by a variety of methods?, Similarly to the production of magnetic stripe cards, to prepare a card material by bonding two sheets, cutting a recessed portion for mounting the IC chip in post-processing The system is becoming mainstream.
通常、 シートには前カードに必要とされる印刷力 S前もって施されている。 Usually, the sheet is pre-applied with the printing power S required for the front card.
P V Cはカレンダ一加工で大量に生産できる上に、 ラミネート適性、 ラミネー ト後のプレス板との剥離性、 エンボス刻印性などの二次加工性に優れているの で、 プラスチックカードの素材として好適な材料である。 PVC is suitable as a plastic card material because it can be mass-produced by calendering and has excellent secondary workability such as lamination suitability, peelability from the press plate after lamination, and embossing stamping. Material.
最近、 世の中のエコロジーブームに乗って、 非 P V C系のカード用素材のニー ズが高まってきており、 ポリスチレン系およびポリエステル系の材料が提案され ている。 Recently, the need for non-PVC-based card materials has been increasing in response to the ecology boom in the world, and polystyrene-based and polyester-based materials have been proposed.
しかし、 これらの非 P V C系のカード用素材である各種の耐衝撃性スチレンや ァクリロ二トリル zブタジエン zスチレン共重合体は、 カード形状に打ち抜いた 時の切断面のバリ (以下 「抜きバリ」 とレゝう) が大きく、 さらに、 カードにェン ボス刻印を行った後、 カードの反り (以下 「エンボスカール」 とレゝう) も大きく なるという問題があった。
また、 非 P V C系カード用素材であるポリエステル系材料としては、 例えば、 重合前のモノマ一の酸成分がテレフタール酸でありジォール成分がェチレングリ コールとシクロへキサンジメタノールであるような、 実質的に非結晶性であるポ リエステル系樹脂がある。 非結晶性ポリエステル系樹脂は P V Cと比較して、 低 温でのラミネート性に優れる上に、 刻印性もよく、 カード状にした場合の繰り返 し曲げ、 捩りへの耐久性に優れるという長所がある。 However, these non-PVC card materials, such as various impact-resistant styrene and acrylonitrile z-butadiene-styrene copolymers, have burrs on the cut surface when punched into a card shape (hereinafter referred to as “burr”). After embossing the card, the warpage of the card (hereinafter referred to as “embossed curl”) also increased. In addition, polyester-based materials that are non-PVC-based card materials include, for example, substantially those in which the monomer component before polymerization is terephthalic acid and the diol components are ethylene glycol and cyclohexanedimethanol. There are non-crystalline polyester resins. Compared to PVC, non-crystalline polyester resin has excellent laminating properties at low temperatures, good engraving properties, and excellent durability against repeated bending and twisting when it is made into a card. is there.
そこで非結晶性ポリエステル系樹脂は好適なカード用素材として注目されてい る力 二次加工性の点でまだ不十分なところがある。 すなわち、 非結晶性ポリエ ステル系樹脂のみからなるカードは高温にさらされると、 力一ドにそりが生じた り、 エンボスカールが生じたりする。 また、 カード形状に打ち抜くときに、 打ち 抜く刃の雄型と雌型のクリアランスでのオーバーシートの伸びが大きく、 フラッ トな打ち抜き断面力 ?得にくレ 。 カードがカールしていたり、 カードの打ち抜き断 面がフラッ トでないと、 手触り力悪いだけでなく、 カードリーダーへの出し入れ 時に断面が機械に引つかかる心配があつた。 Therefore, non-crystalline polyester resins are still insufficient in terms of force secondary processing, which is attracting attention as a suitable card material. That is, when a card made of only an amorphous polyester resin is exposed to a high temperature, the card may be warped or embossed. Furthermore, when the punching into a card shape, greater elongation of the over sheet of male and female clearance blade Nuku out is flat punching member forces? Obtained Nikure. If the card was curled or if the cut surface of the card was not flat, not only the touch was poor, but also the cross section could be caught by the machine when inserting or removing the card from the card reader.
あるいはまた、 プレス板に挟んでラミネートした後、 冷却してから取り出すと き、 プレス板への貼り付き力 ?非常に強力で、 実用可能なレベルの剥離性を得るこ とができないという問題があつた。 Alternatively, after the laminated sandwiched press plate, can and removed from cooled, sticking force of the press plate? Very powerful, the mediation impossible possible to get the release of the practical level Was.
以上述べたように、 非 P V C系であり環境適性に優れた非結晶性ポリエステル 系樹脂はカード用基材に適している面もある力 s、 未だ二次加工性の点において十 分でなく、 カードに使用する場合には要求に応じた二次加工性を満足するように 改良が望まれていた。 発明の開示 As described above, non-PVC-based non-crystalline polyester resin with excellent environmental suitability is not enough in terms of the force s that is suitable for card base material s, and the secondary workability. When used in cards, improvements have been desired to satisfy the required secondary workability. Disclosure of the invention
本発明は上記問題点を解決すべくなされたものであり、 本発明の目的は、 カー ドのそりやエンボスカールが生じない非 p V C系樹脂のプラスチックカード用樹 脂組成物、 シートおよびカードを提供することにある。 また、 本発明の別の目的 は、 カードの打ち抜き断面がフラッ トである非 P V C系樹脂のプラスチックカー ド用樹脂組成物、 シートおよびカードを提供することにある。 さらに本発明の他 の目的は、 プレス板からの剥離性が改良された、 非 P V C系樹脂のプラスチック 力一ド用樹脂組成物、 シートおよびカードを提供することにある。 The present invention has been made to solve the above problems, and an object of the present invention is to provide a resin composition for a plastic card, a sheet, and a card made of a non-pVC resin which do not generate card warpage or emboss curl. To provide. Another object of the present invention is to provide a resin composition, a sheet and a card for a non-PVC-based resin, which has a flat punched-out cross section of the card. Still another object of the present invention is to provide a resin composition for non-PVC-based plastic forceps, a sheet and a card, which have improved releasability from a press plate.
本発明のカード用樹脂組成物の第 1の態様は、 実質的に非結晶性のポリエステ ル系樹脂を主成分とすることを特徴とする。 A first aspect of the resin composition for a card of the present invention is characterized by containing a substantially non-crystalline polyester-based resin as a main component.
本発明のカード用樹脂組成物の第 2の態様は、 プラスチックカードの素材に用
いられる材料であって、 実質的に非結晶性のポリエステル系樹脂に、 ポリエチレ ングリコールとアルキルベンゼンスルホン酸ナトリゥムとを重量比で 1 Z 9〜 9 Z 1の割合で混合したものを、 0 . 1重量%〜 1 . 5重量%の範囲で添加したこ とを特徴とする。 The second embodiment of the resin composition for a card of the present invention is used for a plastic card material. A material obtained by mixing a substantially non-crystalline polyester-based resin with polyethylene glycol and sodium alkylbenzenesulfonate at a weight ratio of 1Z9 to 9Z1, 0.1 It is characterized in that it is added in the range of from 1.5% by weight to 1.5% by weight.
本発明のカード用樹脂組成物の第 3の態様は、 実質的に非結晶性のポリエステ ル系樹脂に、 平均粒径が 5 μ m以下の粉末状ケィ酸および粉末状マグネシゥムシ リケートの少なくとも 1つを、 前記実質的に非結晶性のポリエステル系樹脂に対 して 0 . 5〜 5 . 0重量%の範囲で含有することを特徴とする。 A third embodiment of the resin composition for a card according to the present invention is directed to a substantially non-crystalline polyester-based resin, wherein at least one of a powdered caic acid and a powdered magnesium silicate having an average particle size of 5 μm or less is used. Is contained in the range of 0.5 to 5.0% by weight with respect to the substantially non-crystalline polyester resin.
本発明のカード用樹脂組成物の第 4の態様は、 実質的に非結晶性のポリエステ ル系樹脂に、 平均粒径が 3〜 1 0 μ mの粒状および/または板状の無機フイラ一 を、 前記実質的に非結晶性のポリエステル系樹脂に対して 2〜 1 0重量%の範囲 で含有することを特徴とする。 A fourth aspect of the card resin composition of the present invention, the substantially non-crystalline polyester Le resins, particulate having an average particle size of. 3 to 1 0 mu m and / or plate-like inorganic FILLER one The content is in the range of 2 to 10% by weight based on the substantially non-crystalline polyester resin.
上記カード用樹脂組成物は、 非結晶性のポリエステル系樹脂がテレフタル酸と エチレングリコールと 1 , 4—シクロへキサンジメタノールとの混合物を脱水縮 合させたポリエステル系樹脂であることができる。 The resin composition for a card may be a polyester resin obtained by dehydrating and condensing a mixture of terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol from a non-crystalline polyester resin.
本発明のシートは、 上記カード用樹脂組成物のいずれかを用いて作製されるこ とを特徴とする。 The sheet of the present invention is characterized by being produced using any one of the resin compositions for cards.
本発明のカードは、 上記カード用樹脂組成物のいずれかを用いて作製された層 を有することを特徴とする。 The card of the present invention is characterized by having a layer produced using any one of the above resin compositions for cards.
ここで、 カード用樹脂組成物は、 実質的に非結晶性のポリエステル系樹脂に、 ポリエチレングリコールとアルキルベンゼンスルホン酸ナトリゥムとを重量比で Here, the resin composition for a card is composed of a substantially non-crystalline polyester resin and polyethylene glycol and sodium alkylbenzene sulfonate in a weight ratio.
1 / 9〜 9 Z 1の割合で混合したものを、 0 . 1重量%〜 1 . 5重量%の範囲で 添加した樹脂組成物であり、 該樹脂組成物を用いて作成したシート 2枚からなる カードであることカ?好ましい。 A resin composition in which a mixture of 1/9 to 9Z1 is added in a range of 0.1% by weight to 1.5% by weight. Two sheets prepared using the resin composition are used. it mosquitoes? preferably a made card.
本発明のカードの他の態様は、 最外層であるオーバーシートと内層であるコア シートを有するカードにおいて、 前記コアシートは実質的に非結晶性のポリエス テル系樹脂からなり、 前記オーバーシートはガラス転移温度が 9 0〜 1 4 0 °Cで ある樹脂組成物からなることを特徴とする。 Another aspect of the card of the present invention is a card having an oversheet as an outermost layer and a core sheet as an inner layer, wherein the core sheet is substantially made of an amorphous polyester-based resin, and the oversheet is made of glass. It is characterized by comprising a resin composition having a transition temperature of 90 to 140 ° C.
ここで、 オーバーシートはポリカーボネ一ト系樹脂からなることができる。 また、 非結晶性のポリエステル系樹脂は、 テレフタル酸とエチレングリコール と 1, 4 —シクロへキサンジメタノールとの混合物を脱水縮合したポリエステル 系樹脂であることができる。
発明を実施するための最良の形態 Here, the oversheet can be made of polycarbonate resin. The non-crystalline polyester resin may be a polyester resin obtained by dehydration-condensing a mixture of terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol. BEST MODE FOR CARRYING OUT THE INVENTION
本発明の樹脂組成物は実質的に非結晶性のポリエステル系樹脂を主成分とす る。 The resin composition of the present invention contains a substantially non-crystalline polyester resin as a main component.
ここでいうポリエステルとは、 ジカルボン酸とジオールとの脱水縮合体をい レヽ 本発明に用いられる 「実質的に非結晶性のポリエステル」 とは、 重合前のモ ノマーの酸成分、 またはジオール成分、 あるいは酸成分とジオール成分との両方 が 2成分以上からなる透明な共重合ポリエステル系樹脂であつて、 例えばプレス 融着などの実用上頻繁に行われる熱加工を行っても、 結晶化による白濁を起こさ ないものをいう。 The polyester as used herein refers to a dehydrated condensate of a dicarboxylic acid and a diol. The “substantially non-crystalline polyester” used in the present invention refers to an acid component or a diol component of a monomer before polymerization. Alternatively, it is a transparent copolyester resin in which both the acid component and the diol component are composed of two or more components. What does not happen.
具体的には、 ジカルボン酸としてテレフタル酸、 イソフタル酸、 アジピン酸、 ナフタレンジカルボン酸などが挙げられ、 ジオールとしてはエチレングリコー ル、 ジエチレングリコール、 トリエチレングリコール、 シクロへキサンジメタ ノールなど力 s挙げられる。 酸成分およぴジォ一ル成分の組み合わせは適宜行われ るものとし、 また、 酸成分およびジオール成分がそれぞれ複数選択される場合に は、 その選択も適宜行われるものとする。 Specifically, terephthalic acid as the dicarboxylic acid, isophthalic acid, adipic acid, naphthalene dicarboxylic acid, and examples of the diol ethylene glycol, diethylene glycol, triethylene glycol, force s like Kisanjimeta Nord cyclohexylene. The combination of an acid component and a diol component is appropriately performed. When a plurality of acid components and a plurality of diol components are respectively selected, the selection is appropriately performed.
実質的に非結晶性のポリエステル系樹脂としては、 重合前のモノマーの酸成分 がテレフタル酸であり、 ジォール成分がェチレングリコールとシクロへキサンジ メタノールであるポリエステル系樹脂 (商品名: P E T G、 イーストマンケミカ ル社製) が、 商業的に入手可能なものとして挙げられる。 但し、 本発明において は、 着色剤などの添加剤が添加されていてもよい。 As a substantially non-crystalline polyester resin, a polyester resin in which the acid component of the monomer before polymerization is terephthalic acid and the diol components are ethylene glycol and cyclohexane dimethanol (trade names: PETG, Eastman Chemical Co., Ltd.) is commercially available. However, in the present invention, an additive such as a coloring agent may be added.
本発明においては、 実質的に非結晶性のポリエステル系樹脂に、 ポリエチレン グリコールおよびアルキルベンゼンスルホン酸ナトリゥムを添加することによ り、 カード作製の際のプレス板への貼り付き性を改良することができる。 In the present invention, by adding polyethylene glycol and sodium alkylbenzenesulfonate to a substantially non-crystalline polyester resin, it is possible to improve the sticking property to a press plate during card production. .
実質的に非結晶性のポリエステル系樹脂に添加されるポリエチレングリコール は特に限定されないが、 分子量 1 0 0 0〜5 0 0 0の固体ワックス状のものが、 ペレッ トと混合しやすく、 また、 シートに加工する際に必要とされる熱により揮 発しにくいので好んで使用される。 The polyethylene glycol to be added to the substantially non-crystalline polyester resin is not particularly limited, but a solid wax having a molecular weight of 1,000 to 500,000 can be easily mixed with the pellet, and a sheet. It is preferably used because it is difficult to volatilize due to the heat required when processing into steel.
ここで用いられるアルキルベンゼンスルホン酸ナトリゥムは、 アルキル基の長 さについては特に限定されないが、 ラウリルベンゼンスルホン酸ナトリウムが商 業的に入手しやすく、 好適に使用できる。 The sodium alkylbenzenesulfonate used here is not particularly limited in terms of the length of the alkyl group, but sodium laurylbenzenesulfonate is easily available commercially and can be suitably used.
実質的に非結晶性のポリエステル系樹脂に添加されるポリエチレングリコール とアルキルベンゼンスルホン酸ナトリゥムの比率は、 重量比で 1 Z 9〜 9 / 1の 範囲が好ましい。 添加されるポリエチレングリコールとアルキルベンゼンスルホ
ン酸ナトリゥムの比率がかかる範囲外のときは、 ラミネート後のプレス板からの 剥離性カ环十分となる。 The ratio of polyethylene glycol to sodium alkylbenzene sulfonate added to the substantially non-crystalline polyester resin is preferably in the range of 1Z9 to 9/1 by weight. Polyethylene glycol and alkylbenzene sulfo added When the ratio of sodium phosphate is out of the above range, the peelability from the press plate after lamination is sufficient.
一般に、 磁気ストライプカード、 I Cカード等のプラスチックカードは複数枚 のシートの積層からなり、 最外層をオーバ一シート、 内層をコアシートという。 ラミネートされるコア層とオーバ一層のシートサイズは、 カードメーカーによ り異なりコア層よりオーバ一層の方が若干小さいこともある。 そのため、 ォー バー層の剥離性のみならず、 コア層についてもプレス板からの剥離性を改良して おく必要がある。 Generally, a plastic card such as a magnetic stripe card or an IC card is formed by laminating a plurality of sheets, and the outermost layer is called an over-sheet and the inner layer is called a core sheet. The sheet size of the core layer and the overlayer to be laminated differs depending on the card manufacturer, and the overlayer may be slightly smaller than the core layer. Therefore, it is necessary to improve not only the releasability of the overlayer but also the core layer from the press plate.
実質的に非結晶性のポリエステル系樹脂を、 コア層とオーバ一層とからなる カードのコア層として使用する場合あるいはオーバー層として使用する場合、 ま たは、 コア層のみからなるカードのコア層として使用する場合のいずれでも、 ポ リエチレングリコールおよびアルキルベンゼンスルホン酸ナトリゥムの添加量 は、 非結晶性のポリエステル系樹脂 1 0 0重量%に対して、 0 . 1重量%〜 1 . 5重量%の範囲が好ましく、 0 . 2重量%〜 1 . 5重量%がさらに好ましく、 0 . 5重量%〜 1 . 0重量%が特に好ましい。 When a substantially non-crystalline polyester resin is used as a core layer of a card comprising a core layer and an over layer, or used as an over layer, or as a core layer of a card comprising only a core layer In any case, the added amount of polyethylene glycol and sodium alkyl benzene sulfonate is in the range of 0.1% by weight to 1.5% by weight based on 100% by weight of the amorphous polyester resin. It is preferably from 0.2% to 1.5% by weight, more preferably from 0.5% to 1.0% by weight.
ポリエチレングリコールぉよびァルキルべンゼンスルホン酸ナトリウムの添加 量が 0 . 1重量%以上ならば、 実用可能なレベルの剥離性が得られ、 0 . 2重 量%以上ならば十分な剥離性力得られる。 また、 これらの添加量が 1 . 5重量% 以下ならば、 シ一トの物性や印刷適性にも優れたものとなる。 ここで印刷適性と は、 シ一ト上に印刷する際に用いるインクとシートとの馴染みの良さを意味する ものとする。 印刷適性が悪い場合には、 インクのはじき等が生じてシートにきれ いに印刷ができない。 When the amount of polyethylene glycol and sodium alkylbenzenesulfonate is 0.1% by weight or more, a practical level of releasability is obtained, and when it is 0.2% by weight or more, sufficient releasability is obtained. . When the amount of these additives is 1.5% by weight or less, the sheet has excellent physical properties and printability. Here, the printability means the familiarity between the ink used when printing on a sheet and the sheet. If the printability is poor, ink repelling may occur, making it impossible to print cleanly on the sheet.
なお、 上記樹脂組成物は帯電防止性にも優れており、 静電気による印刷時の シートの送り不良ゃィンキの飛びが発生しにく く、 さらにプレス作業においてス パークが起こりにくいという利点もある。 The resin composition is also excellent in antistatic properties, has the advantage that the sheet is not easily fed during printing due to static electricity, does not cause jumps, and has the advantage that sparks are less likely to occur during press work.
本発明においては、 実質的に非結晶性であるポリエステル系樹脂に、 平均粒径 が 5 μ m以下の粉末状ケィ酸および Zまたは粉末状マグネシゥムシリケートを、 該ポリエステル系樹脂 1 0 0重量0 /0に対して 5〜 5 . 0重量0 /0含有すること により、 カードの透明性が確保され、 作製される力一ドは刻印部分の割れ力生じ ず、 かつ、 フラットな打ち抜き断面力 s得られる。 In the present invention, a powdery keic acid having an average particle diameter of 5 μm or less and Z or a powdery magnesium silicate are added to a substantially non-crystalline polyester resin, and the polyester resin is added in an amount of 100% by weight. 0/0 5 against 5. by 0 weight 0/0 by containing, secured the transparency of the card, the force one de made does not occur cracking force of engraved portions, and flat punching member forces s obtained.
粉末状ケィ酸は透明性を有するが硬く、 一方、 粉末状マグネシウムシリケート は軟らかいが透明性が低下する、 という性質を有する。 したがって、 シートまた はカード等に要求される特性に応じて適宜選択されるとよい。 また、 粉末状ケィ
酸と粉末状マグネシゥムシリケ一トは単独で用いられてもよいが、 併用してもよ いので、 カード等に要求される性質等に応じて併合割合など適宜選択されるとよ い。 ただし、 ポリエステル系樹脂に対する含有量は 0 . 5〜 5 . 0重量%であ る。 Powdered caustic acid is transparent but hard, whereas powdered magnesium silicate is soft but has reduced transparency. Therefore, it may be appropriately selected according to the characteristics required for the sheet or the card. In addition, powdery The acid and the powdery magnesium silicate may be used alone, but may be used in combination. Therefore, the combination ratio and the like may be appropriately selected according to the properties required for the card and the like. However, the content with respect to the polyester resin is 0.5 to 5.0% by weight.
粉末状ケィ酸の添加量が 0 . 5重量%以上ならば、 打ち抜き断面の改良効果が 得られる。 なお、 粉末状ケィ酸の添加量が 5 . 0重量%を越えても透明性の低下 はないが、 硬くなるので打ち抜き刃の磨耗や刻印部分の割れが起こり易くなる。 粉末状マグネシゥムシリケ一トの添加量が 0 . 5重量%以上ならば、 打ち抜き断 面の改良効果が得られる。 一方、 粉末状マグネシゥムシリケートの添加量が 5 . 0重量%を越えても打ち抜き刃の磨耗や刻印部分の割れは生じないが、 シートの 透明性は低下する。 If the amount of the powdered caic acid is 0.5% by weight or more, the effect of improving the punched cross section can be obtained. Although the transparency does not decrease even if the amount of the powdered kaic acid exceeds 5.0% by weight, the hardness becomes hard, so that the abrasion of the punching blade and the cracking of the engraved portion are liable to occur. If the amount of the powdered magnesium silicate is 0.5% by weight or more, the effect of improving the punched cross section can be obtained. On the other hand, if the amount of the powdered magnesium silicate exceeds 5.0% by weight, abrasion of the punching blade and cracking of the stamped portion do not occur, but the transparency of the sheet is reduced.
ここで用いられる粉末状ケィ酸および粉末状マグネシゥムシリケートは、 平均 粒径が 5 μ m以下であること力 s好ましい。 平均粒径が 5 mより大きい粉末状ケ ィ酸を用いると、 カード形状に打ち抜く際に打ち抜き刃力'磨耗し易く、 またシー トの耐衝撃性が低下し、 カードに刻印を打つたときに刻印部分が割れることがあ るからである。 また、 平均粒径が 5 mより大きい粉末状マグネシゥムシリケー トを用いると、 透明性が低下し、 図柄や文字等の視認性カ 氐下することがあるか らである。 It is preferable that the powdery kaic acid and the powdery magnesium silicate used here have an average particle size of 5 μm or less. If powdered citric acid having an average particle size of more than 5 m is used, the punching blade force is easily worn when punching into a card shape, and the impact resistance of the sheet is reduced. This is because the stamp may be broken. Also, if powdered magnesium silicate having an average particle size of more than 5 m is used, transparency is reduced, and visibility of a pattern or a character may be reduced.
通常、 磁気ストライプカード、 I Cカード等のプラスチックカードは、 複数枚 のシートの積層からなり、 最外層をオーバーシート、 内層をコアシートという。 作製されたカードがフラッ トな打ち抜き断面を有することを目的とする場合に は、 コアシートおよびオーバーシートの少なくとも一方が、 このような粉末状ケ ィ酸および/または粉末状マグネシゥムシリケートを含有する樹脂からなればよ いが、 以下の理由からオーバーシートであることが好ましい。 すなわち、 通常、 コアシートは隠蔽性を必要とし、 また印刷層あるいは印刷層の下地になることが 要求されるために、 酸化チタン力 ?添加されている。 そのためコアシートは、 打ち 抜き工程で打ち抜き刃の雄型と雌型のクリアランスで大きく伸びるということは 起こりにくい。 したがって打ち抜き加工性能等に劣るォ一パーシートに好んで使 用される。 Normally, plastic cards such as magnetic stripe cards and IC cards are formed by laminating a plurality of sheets, and the outermost layer is called an oversheet and the inner layer is called a core sheet. If the card produced is intended to have a flat stamped cross-section, at least one of the core sheet and the oversheet contains such a powdered kaic acid and / or a powdered magnesium silicate. However, it is preferable to use an overseat for the following reasons. That is, usually, core sheet requires hiding property, and to be a base of the print layer or the print layer is required, which is titanium oxide power? Added. For this reason, it is unlikely that the core sheet will greatly expand due to the clearance between the male and female dies in the punching process. Therefore, it is preferably used for paper sheets with poor punching performance.
本発明においては、 実質的に非結晶性であるポリエステル系樹脂に、 平均粒径 が 3〜 1 0 mの粒状および または板状の無機フイラ一を、 該非結晶性ポリェ ステル系樹脂 1 0 0重量0 /0に対して 2〜 1 0重量%含有することにより、 作製さ れるカードのエンボス力一ル性を改良することができる。
ここで用いられる無機フィラーの種類は、 その形状が粒状または板状であり、 平均粒子が 3〜 1 0 z^ mであれば特に制限されるものではない。 具体的には、 タ ルク、 マグネシウムシリケート、 炭酸カルシウム、 シリカ、 マイ力あるいはこれ らの混合物等が挙げられる。 すなわちガラス繊維等の針状のものは含まない。 無機フィラーの平均粒径が 3 m以上ならばェンボスカールの発生を防止する 効果が大きく、 1 0 m以下ならば得られたシートの耐衝撃性も十分で、 カード に刻印を打ったときに刻印部分が割れることがない。 In the present invention, a granular and / or plate-like inorganic filler having an average particle diameter of 3 to 10 m is added to the substantially non-crystalline polyester resin by adding 100% by weight of the non-crystalline polyester resin. by containing 2-1 0% by weight relative to the 0/0, it is possible to improve the embossing force one le of the card to be manufactured. The type of the inorganic filler used here is not particularly limited as long as its shape is granular or plate-like and the average particle is 3 to 10 z ^ m. Specific examples include talc, magnesium silicate, calcium carbonate, silica, myriki, or a mixture thereof. That is, needle-like materials such as glass fibers are not included. When the average particle size of the inorganic filler is 3 m or more, the effect of preventing the occurrence of emboss curl is great, and when the average particle size is 10 m or less, the impact resistance of the obtained sheet is sufficient. Does not break.
非結晶性ポリエステル系榭脂に対する無機フィラーの添加量が 2〜 1 0重量% の範囲であるならば、 ェンボス力一ルの改良効果が大きく、 かつ刻印部分の割れ の問題も生じない。 When the amount of the inorganic filler added to the non-crystalline polyester resin is in the range of 2 to 10% by weight, the effect of improving the embossing force is large, and the problem of cracking of the engraved portion does not occur.
オーバーシートおよびコアシートを有する力一ドにおいてエンボスカールの改 良を目的とする場合には、 少なくとも一方が無機フィラーを含有するかかる樹脂 からなればよいが、 以下の理由からコアシートであることが好ましい。 For the purpose of improving the emboss curl in a force having an oversheet and a core sheet, at least one of them may be made of such a resin containing an inorganic filler, but the core sheet may be used for the following reasons. preferable.
すなわち、 通常、 コアシートには個人情報等の印刷が施されておりオーバー シートで保護されている。 オーバーシートは、 コアシートの印刷の保護さらには 印刷を装飾するために用いられ、 層厚は薄く透明であることが多い。 一般的に カードにはリーダライタの特性から相応の厚さと、 光に対する高い隠蔽性と反射 性とが要求されるので、 コアシートは層厚が厚く、 酸化チタン等の着色剤が添加 されていることが多い。 エンボス加工はォ一パーシートとコアシ一トとを積層し た後に施されるので、 エンボスカールの改良を目的とする場合には、 コアシート およびオーバーシートの少なくとも一方が無機フィラ一を含有するかかる樹脂か らなるシートであればよい。 ただし、 上述した通り、 通常、 コアシートはォー バーシ一トより厚いこと、 また、 オーバーシートは透明性を有することから、 コ ァシートに好んで使用される。 That is, the core sheet is usually printed with personal information and the like, and is protected by an oversheet. Oversheets are used to protect the print of the core sheet and to decorate the print, and are often thin and transparent. In general, the card is required to have an appropriate thickness and high light concealment and reflection properties due to the characteristics of the reader / writer, so the core sheet is thick and contains a coloring agent such as titanium oxide. Often. Since the embossing process is performed after laminating the upper sheet and the core sheet, if the purpose is to improve the emboss curl, at least one of the core sheet and the over sheet is made of such a resin containing an inorganic filler. Any sheet may be used. However, as described above, usually, the core sheet is preferably used for the core sheet because the core sheet is thicker than the over sheet and the over sheet has transparency.
本発明においては、 以上説明した樹脂組成物を用いて、 例えば溶融押し出し法 等の公知の方法によりシートに成形することができ、 また、 磁気ストライプカー ドゃ I Cカードなどのプラスチックカードを製造することもできる。 なお、 コア シートには帯電防止剤等を添加してもよい。 In the present invention, the resin composition described above can be used to form a sheet by a known method such as, for example, a melt extrusion method, or a magnetic stripe card or a plastic card such as an IC card. Can also. Note that an antistatic agent or the like may be added to the core sheet.
本発明においては、 コアシート力実質的に非結晶性のポリエステル系樹脂から なり、 オーバーシートがガラス転移温度 9 0〜 1 4 0 °Cの樹脂からなる構成をと ることにより、 カードの耐熱温度を上げることができる。 In the present invention, the core sheet is made of a substantially non-crystalline polyester resin, and the oversheet is made of a resin having a glass transition temperature of 90 to 140 ° C., whereby the heat resistance temperature of the card is improved. Can be raised.
かかるコアシートは実質的に非結晶性のポリエステル系樹脂に添加剤、 例えば 酸化チタン等の着色剤や滑り剤、 帯電防止剤等を添加して、 溶融押し出し法等に
よって得ることができる。 Such a core sheet is obtained by adding an additive, for example, a coloring agent such as titanium oxide, a slipping agent, an antistatic agent, etc. to a substantially non-crystalline polyester resin, and applying a melt extrusion method or the like. Therefore, it can be obtained.
オーバーシートのガラス転移温度が 9 0 °C以上ならばカードとしての耐熱性が 十分改良され、 1 4 0 °C以下ならばラミネートの際、 コアシ一トとの融着性が十 分得られる。 したがって融着性を改良するために高温にする必要がないので、 コ ァシートが流動化することもなく、 所望のカード厚みより薄くなることもない。 ガラス転移温度は周波数 1 H zでの動的粘弾性の測定における損失弾性率の ピークから求める。 具体的には、 粘弾性スぺクトロメーターを用いて、 資料に周 波数 1 H zの正弦波状に変化する歪みを加えながら、 引張弾性率の温度依存性を 測定する。 測定条件は試料厚み 1 mm、 最大歪み 1 %、 昇温速度 4 °CZ分で、 室 温からスタートし、 引張損失弾性率 E " 力 s極大のピークを示し、 引張貯蔵弾性率 E ' が大きく低下し始める付近の温度をガラス転移温度とした。 If the glass transition temperature of the oversheet is 90 ° C or more, the heat resistance of the card is sufficiently improved, and if it is 140 ° C or less, sufficient adhesion to the core sheet can be obtained during lamination. Thus, there is no need to raise the temperature to improve the fusibility, so the co-sheet does not flow and does not become thinner than the desired card thickness. The glass transition temperature is determined from the peak of the loss modulus in the measurement of dynamic viscoelasticity at a frequency of 1 Hz. Specifically, the temperature dependence of the tensile modulus is measured using a viscoelastic spectrometer while applying a sinusoidally changing strain at a frequency of 1 Hz to the sample. The measurement conditions were as follows: the sample thickness was 1 mm, the maximum strain was 1%, the heating rate was 4 ° CZ min., Starting from room temperature, the tensile loss modulus E "showed a peak at the maximum force s , and the tensile storage modulus E 'was large. The temperature near the beginning of the decrease was defined as the glass transition temperature.
ここで好ましく用いられるオーバ一シートとしては、 非結晶性ポリエステル系 樹脂と熱融着可能であるとの理由から、 ポリカーボネート (以下 「P C」 と略す こともある) 系樹脂が挙げられる。 また他にも、 脂肪族ジカルボン酸を共重合し た共重合 P Cや、 P Cに可塑剤を添加してガラス転移温度を上記範囲となるよう に調節したもの等も使用できる。 なお、 これらの樹脂に滑り剤や帯電防止剤等を 添加してもよい。 シートは溶融押し出し法等公知の方法によつて得ることができ る。 As an oversheet preferably used herein, a polycarbonate (hereinafter sometimes abbreviated as “PC”) resin is cited because it can be heat-fused with an amorphous polyester resin. In addition, copolymerized PC obtained by copolymerizing an aliphatic dicarboxylic acid, one obtained by adding a plasticizer to PC and adjusting the glass transition temperature to fall within the above range, and the like can also be used. Note that a slipping agent, an antistatic agent, and the like may be added to these resins. The sheet can be obtained by a known method such as a melt extrusion method.
なお、 本発明においては、 カードに要求される特性に応じて、 二次加工性を改 良するための上記手段を 2つ以上組み合わせて使用することもできる。 組み合わ せて使用する場合には、 それぞれの二次加工性を共に改良することができる。 以下に、 本発明を実施例を用いて具体的に説明する。 実施例 In the present invention, two or more of the above means for improving the secondary workability can be used in combination according to the characteristics required for the card. When used in combination, the secondary workability of each can be improved together. Hereinafter, the present invention will be described specifically with reference to Examples. Example
実例 I一 1 Example I-1
実質的に非結晶性であるポリエステル系樹脂として、 P E T G 6 7 6 3 (ィー ストマンケミカル社製) を 1 0 0重量部、 白色顔料として酸化チタンを 1 0重量 部、 およびポリエチレングリコール (分子量 3 0 0 0 ) とラウリルベンゼンスル ホン酸ナトリウムの混合物あるいは他の滑り剤を表 1に示すように用いて、 Tダ ィ押出法により厚さ 4 0 0 /^ mのシートを得た。 As a substantially non-crystalline polyester resin, 100 parts by weight of PETG 667 (manufactured by Yeastman Chemical Company), 10 parts by weight of titanium oxide as a white pigment, and polyethylene glycol (molecular weight 3 A sheet having a thickness of 400 / m was obtained by a T-die extrusion method using a mixture of (0000)) and sodium laurylbenzenesulfonate or another slip agent as shown in Table 1.
次いで、 得られたシートを 2 0 O mm X 2 0 0 mmの大きさに力ッ トし、 この カットしたシートを 2枚重ねて 2枚のクロムメッキ鋼板で挟み、 プレス温度 1 2 0 °C、 試料圧力 5 0 k g f Z c m2で 1 0分間保持した。 次いで、 これを室温まで
冷却した後クロムメツキ鋼板を取り出し、 2枚のクロムメツキ鋼板を引き剥がし た。 クロムメツキ鋼板を引き剥がすのに必要な力を触感で評価して、 メツキ板と の剥離性の評価を行った。 Next, the obtained sheet was pressed to a size of 200 mm × 200 mm, and two cut sheets were stacked and sandwiched between two chromium-plated steel sheets, and the pressing temperature was set at 120 ° C. The sample pressure was kept at 50 kgf Z cm 2 for 10 minutes. Then bring this to room temperature After cooling, the chrome plated steel sheet was taken out and the two chrome plated steel sheets were peeled off. The force required to peel off the chrome plated steel plate was evaluated by tactile sensation, and the peelability from the plated plate was evaluated.
また、 印刷適性を評価するため、 得られた押し出しシートの表面張力を濡れ指 数標準液 (ナカライテスク社製) を用いて測定した。 In order to evaluate printability, the surface tension of the obtained extruded sheet was measured using a wet index standard solution (manufactured by Nacalai Tesque).
ただし評価基準は、 表中の 「メツキ板との剥離性」 については、 容易に剥がす ことができるものを 「A」 、 抵抗はあるが実用可能な剥離性を示すものを 「B」 、 全く剥離できないものを 「C] とした。 また、 「印刷適性」 について は、 表面張力が 38 d y n e/c m以上あるものを 「A」 、 36 d y n eZ c m以上、 38 d y n eZc m未満のものを 「B」 、 36 d y n e / c m未満の ものを 「C」 とした。 However, the evaluation criteria were as follows: Regarding the "peelability from the plating plate" in the table, "A" indicates that it can be easily peeled, and "B" indicates that it exhibits peelability with resistance but practical. Those that could not be evaluated were designated as “C.” The “Printability” was rated “A” for those with a surface tension of 38 dyne / cm or more, and “B” for those with a surface tension of 36 dyn eZcm or more and less than 38 dyne eZcm. And less than 36 dyne / cm were designated as “C”.
なお、 表中の滑り剤の添加量は、 PETG 6 763を 1 00としたときの重 量0 /0であり、 PEGはポリエチレングリコールの略号であり、 LB Sはラウリル ベンゼンスルホン酸ナトリゥムの略号である。 実例 I一 2〜 I— 5、 対照 I一;!〜 I— 8 The addition amount of the lubricant in the table is the Weight 0/0 when the PETG 6 763 1 00 and, PEG is an abbreviation for polyethylene glycol, LB S in abbreviation Natoriumu laurylbenzenesulfonate is there. Examples I-1 2 to I-5, Control I-1; ~ I— 8
実例 I一 1において、 滑り剤の種類および添加量を表 1〜表 3に示すように変 更した以外は実例 1— 1と同様にして、 評価用サンプルを作製した。 A sample for evaluation was prepared in the same manner as in Example 1-1 except that the type and amount of the slipping agent in Example I-11 were changed as shown in Tables 1 to 3.
得られた評価用サンプルについて、 実例 I— 1と同様の評価を行った。 これら の評価結果を表 1〜表 3にまとめて示した。 About the obtained evaluation sample, the same evaluation as Example I-1 was performed. Tables 1 to 3 summarize the evaluation results.
[表 1] [table 1]
実 施 例 Example
1-1 1-2 1-3 1-4 1-5 滑り剤の種類 PEG 0.02重量% PEG 0.18重量% PEG 0.5重量% PEG 0.15重量% PEG 1.35重量1 ¾ および直 LBS 0.18重量% LBS 0.02重量% LBS 0.5重量% LBS 1.35重量% LBS 0.15重量%1-1 1-2 1-3 1-4 1-5 types PEG 0.02 wt% of slip agent PEG 0.18 wt% PEG 0.5 wt% PEG 0.15 wt% PEG 1.35 wt 1 ¾ and straight LBS 0.18 wt% LBS 0.02 wt% LBS 0.5% by weight LBS 1.35% by weight LBS 0.15% by weight
PEG/LBSの 1/9 9/1 5/5 1/9 9/1 重量比率 1/9 9/1 5/5 1/9 9/1 weight ratio of PEG / LBS
総添加量 0.2重量% 0.2重量% 1.0重量% 1.5重量% 1.5重量% メ ッキ板 B B A A A との剥離性 Total addition amount 0.2% by weight 0.2% by weight 1.0% by weight 1.5% by weight 1.5% by weight Peeling property from Mac board B B A A A
印刷適正 A A A B B
[表 2 ] Printability AAABB [Table 2]
[¾ 3 ] [¾ 3]
実例 I— 1 I 一 5、 対照 I _ 1 I _ 8より明らかなように、 本発明の構成 からなるカードは剥離性および印刷適性に優れていることがわかる。 また、 上述 した実例は白色顔料を含有した実質的に非結晶性ポリエステル系樹脂からなる シートを 2枚ラミネートしたものである力'、 コア層とオーバー層とからなる力一 ドでも同様の結果を得ることができる。 もちろん、 その他の構成であっても同様 である。 実例 II一 1 As is clear from Example I-1 I-15 and Control I_1 I_8, the card having the structure of the present invention was found to be excellent in peelability and printability. In addition, in the above-described example, the same result is obtained with a force obtained by laminating two sheets of substantially non-crystalline polyester resin containing a white pigment, and a force obtained by forming a core layer and an over layer. Obtainable. Of course, the same applies to other configurations. Example II-1
[コアシートの作製] [Preparation of core sheet]
非結晶性ポリエステルとして P E TG 6 7 6 3 (ィ一ストマンケミカル社製) に酸化チタンをその濃度が 1 0重量%となるように添加したものを Tダイ押し出
し法によって厚さ 560 mのコアシートを得た。 T-die extrusion of non-crystalline polyester obtained by adding titanium oxide to PE TG 6763 (manufactured by Istman Chemical Co., Ltd.) to a concentration of 10% by weight. A core sheet having a thickness of 560 m was obtained by the coating method.
[オーバーシートの作製] [Production of oversheet]
結晶性ポリエステルとして PETG6763の 100重量0 /0にラウリルべンゼ ンスルホン酸ナトリウムを 0. 5重量0 /0、 分子量 3000のポリエチレングリ コールを 0. 5重量%添加したものに、 添加剤として平均粒径 3 mのケィ酸を 0. 6重量%混合し、 Tダイ押し出し法によって厚さ 100 mのオーバーシー トを得た。 なお、 表中の添加剤の添加量は PETG 6763を 100としたとき の重量%である。 0.5 weight 0/0 to 100 weight 0/0 lauryl base sodium Nze Nsuruhon acid PETG6763 as a crystalline polyester, polyethylene glycol of molecular weight 3000 to those obtained by adding 0.5 wt%, average particle size as an additive 0.6% by weight of 3 m of citric acid was mixed, and an oversheet having a thickness of 100 m was obtained by a T-die extrusion method. The amounts of the additives shown in the table are% by weight with PETG 6763 being 100.
[カードの作製] [Preparation of card]
得られたコアシートの両面にシルクスクリーン印刷法で絵柄を印刷し、 両面に オーバーシートを重ね、 2枚のクロムメツキ鋼板で挟み、 プレス温度 1 20° (:、 試料圧力 20 k g f Zcm2にて 5分間保持した後、 室温まで冷却し、 クロムメッ キ板から取り出し、 雄型と雌型からなる打ち抜き刃でカード形状に打ち抜いた。 なお、 雄型と雌型のクリアランスは 30 mであった。 A pattern is printed on both sides of the obtained core sheet by the silk screen printing method, oversheets are overlaid on both sides, sandwiched between two chrome plated steel sheets, and pressed at a temperature of 120 ° (:, sample pressure of 20 kgf Zcm 2 at 5 kgf Zcm 2) . After holding for 1 minute, it was cooled to room temperature, taken out of the chrome plating plate, and punched into a card shape with a punching blade composed of a male die and a female die, with a clearance of 30 m between the male die and the female die.
得られた評価用カードサンプルに、 電動ェンボッサーを用いて以下に示す方法 でエンボス刻印を行い、 チッパーにて刻印部分の箔を転写し、 下記基準に従い評 価を行った。 なお、 平均粒径は以下のようにして求めた。 The obtained card sample for evaluation was embossed by the following method using an electric enbosser, the foil of the engraved portion was transferred by a chipper, and the evaluation was performed according to the following criteria. The average particle size was determined as follows.
エンボス刻印: Embossed stamp:
J I S X- 6301にある 「6. エンボス文字の位置 ·形!犬♦寸法」 に準じ て、 「1234 5678 9012」 と刻印した。 In accordance with “6. Position of embossed characters and shape! Dog dimensions” in JIS X-6301, “1234 5678 9012” was engraved.
[平均粒径の測定] [Measurement of average particle size]
沈降式粒度分布測定装置 S A— CP 2— 20 ( (株) 島津製作所製) により測 定された粒度分布データからモード径を求めて、 平均粒径とした。 The mode diameter was determined from the particle size distribution data measured by a sedimentation type particle size distribution analyzer S A—CP 2-20 (manufactured by Shimadzu Corporation), and the average particle size was determined.
[評価] [Evaluation]
得られた評価用カードサンプルの打ち抜き断面のフラッ ト性を指触で評価し た。 コアシートに印刷された絵柄の視認性、 および刻印部分の文字割れを目視評 価した。 その結果を表 4に示す。 なお、 評価基準は下記の通りである。 打ち抜き断面の評価基準: The flatness of the punched cross section of the obtained evaluation card sample was evaluated by finger touch. The visibility of the pattern printed on the core sheet and the breakage of the characters in the engraved part were visually evaluated. The results are shown in Table 4. The evaluation criteria are as follows. Evaluation criteria for punched section:
A ザラツキが全く感じられない A Zaratsuki is not felt at all
B ザラツキがわずかに感じられる B Slightly noticeable
C ザラツキが大きい C Zaratsuki is large
絵柄の視認性の評価基準:
A 絵柄がはつきりと視認できる Evaluation criteria for visibility of picture: A The pattern is clearly visible
B わずかにくもった感じ B Slightly cloudy feeling
C くもった感じ C
刻印部分の割れの評価基準: Evaluation criteria for cracks in the engraved part:
A 割れが見られない A No crack is seen
B 割れている部分がある 実例 II— 2 〜Π— 5、 対照 II— 1 〜11一 9 B There is a cracked part. Example II—2 to Π—5, Control II—1-111 to 9
実例 Π— 1において、 オーバーシートに添加される添加剤の種類と量を表 4に 示すように変更した以外は実例 II一 1と同様にして、 評価用カードサンプルを作 製し、 実例 II— 1と同様の評価を行った。 In Example II-1, a card sample for evaluation was prepared in the same manner as in Example II-11 except that the types and amounts of additives added to the oversheet were changed as shown in Table 4. The same evaluation as in 1 was performed.
得られた結果をまとめて表 4に示す。 Table 4 summarizes the obtained results.
[表 4 ] [Table 4]
注) 添加剤の添加量の単位は 重量% である (
表 4から明らかなように、 平均粒径が 5 以下のケィ酸および Zまたはマグ ネシゥムシリケートを含有する樹脂をオーバ一シートとして用いたカードは、 亥 IJ 印部分の文字割れ力5'生じることなく、 透明性に優れ、 打ち抜き断面がフラッ トな カードであった。 実例 III一 1 Note) The unit of the additive amount is% by weight ( As is evident from Table 4, a card using a resin containing caic acid with an average particle size of 5 or less and Z or magnesium silicate as an over-sheet produces a character breaking force of 5 'at the IJ mark. It was a transparent card with excellent transparency and a punched cross section. Example III-1
[コアシートの作製] [Preparation of core sheet]
非結晶ポリエステルとして P E T G 6 7 6 3 (ィーストマンケミカル社製) に、 酸化チタンをその濃度が 5重量%となるように添加したものに、 無機フィ ラーとして表 5に示す平均粒径 4 mのタルク 5重量%を混合して、 Tダイ押し 出し法によって厚さ 5 6 0 のコアシ一トを得た。 なお、 表中のフィラーの添 加量は P E T G 6 7 6 3を 1 0 0としたときの重量%である。 A non-crystalline polyester made by adding titanium oxide to PETG 676 3 (manufactured by Yeastman Chemical Co., Ltd.) to a concentration of 5% by weight, and having an average particle size of 4 m shown in Table 5 as an inorganic filler 5% by weight of talc was mixed, and a core sheet having a thickness of 560 was obtained by a T-die extrusion method. Note that the amount of filler added in the table is% by weight when PETG 667 is 100.
[オーバーシートの作製] [Production of oversheet]
非結晶ポリエステルとして P E T G 6 7 6 3 (イーストマンケミカル社製) 1 0 0重量部に対して、 ラウリルベンゼンスルホン酸ナトリウムを 0 . 5重量0 /0、 分子量 3 0 0 0のポリエチレングリコールを 0 . 5重量%添加し、 Tダイ押し出 し法によって、 厚さ 1 0 0 // mのオーバーシートを得た。 Respect PETG 6 7 (manufactured by Eastman Chemical Company) 6 3 1 0 0 part by weight as a non-crystalline polyester, 0 sodium lauryl benzene sulfonate. 5 wt 0/0, the molecular weight 3 0 0 0 polyethylene glycol 0. 5% by weight was added, and an oversheet having a thickness of 100 // m was obtained by a T-die extrusion method.
[カードの作製] [Preparation of card]
得られたコアシートの両面に絵柄を印刷し、 両面にオーバーシートを重ね、 2 枚のクロムメッキ鋼板で挟み、 プレス温度 1 2 0 °C、 試料圧力 2 0 k g f / c m2 にて 5分間保持した後、 室温まで冷却し、 クロムメツキ板から取り出し、 雄型と 雌型とからなる打ち抜き刃でカード形状に打ち抜いて評価用カードサンプルを作 製した。 得られた評価用カードサンプルに、 電動ェンボッサーを用いて実施例 II 一 1で説明したようなエンボス刻印を行い、 チッパーを用いて刻印部分の箔を転 写し、 下記評価基準に従い評価を行った。 なお、 無機フィラーの平均粒径は以下 のようにして求めた。 A pattern is printed on both sides of the obtained core sheet, the oversheet is overlaid on both sides, sandwiched between two chrome-plated steel sheets, and kept at a press temperature of 120 ° C and a sample pressure of 20 kgf / cm2 for 5 minutes. After cooling to room temperature, it was taken out of the chrome plating plate and punched into a card shape with a punching blade composed of a male die and a female die to produce a card sample for evaluation. The obtained card sample for evaluation was embossed as described in Example II-11 using an electric enbosser, the foil at the engraved portion was transferred using a chipper, and evaluated according to the following evaluation criteria. The average particle size of the inorganic filler was determined as follows.
[平均粒径の測定] [Measurement of average particle size]
沈降式粒度分布測定装置 S A— C P 2— 2 0 ( (株) 島津製作所製) から測定 された粒度分布データからモ一ド径を求めて、 平均粒径とした。 The mode diameter was determined from the particle size distribution data measured by a sedimentation type particle size distribution analyzer S A—C P 2—20 (manufactured by Shimadzu Corporation), and the average particle size was determined.
[評価] [Evaluation]
得られた評価用カードサンプルのエンボスカールを、 J I S X— 6 3 0 1 ( 4 . 2 . 5 「カードの反り」 ) に従って測定した。 また刻印部分の文字割れを 目視評価を行った。 これらの結果をまとめて表 5に示す。
P /02545 The emboss curl of the obtained card sample for evaluation was measured in accordance with JISX-6301 (4.2.5 "Curve of card"). In addition, the character breakage of the engraved part was visually evaluated. Table 5 summarizes these results. P / 02545
14 実例 III— 2〜III— 6、 対照 ΠΙ— 1〜 III— 6 14 Example III—2 to III—6, control ΠΙ—1 to III—6
実例 III一 1において、 コアーシ一トに添加される無機フィラーの種類と量を表 5に示すように変更した以外は実例 ΙΠ— 1と同様にして、 評価用カードサンプル を作製し、 実例 ΙΠ— 1と同様の評価を行った。 In Example III-11, a card sample for evaluation was prepared in the same manner as in Example III-1, except that the type and amount of the inorganic filler added to the core sheet were changed as shown in Table 5. The same evaluation as in 1 was performed.
得られた結果をまとめて表 5に示す。 Table 5 summarizes the obtained results.
[表 5 ] [Table 5]
表 5から明らかなように、 平均粒径が 3〜 1 0 mの無機フィラーを 2〜 1 0 重量%含有する樹脂をコアシートとして用いたカードは、 エンボスカールがな く、 かつ、 刻印部分 (エンボス加工部分) の文字割れが生じることのないフラッ トなカードであった。 実例 IV— 1 As is clear from Table 5, a card using a resin containing an inorganic filler having an average particle diameter of 3 to 10 m and containing 2 to 10% by weight as a core sheet has no embossed curl, and has an engraved portion ( It was a flat card with no character breakage (embossed part). Example IV—1
[コアシートの作製]
酸成分がテレフ夕ル酸、 ジォ一ル成分がェチレングリコール (約 7 0モル % ) とシクロへキサンジメタノール (約 3 0モル0 /o) の非結晶性ポリエステルである P E T G (イーストマンケミカル社製) 1 0 0重量部に対して酸ィ匕チタンを 1 0 重量部添加し、 Tダイ押し出し法により厚さ 3 0 0 / mの白色コアシートを得 た。 [Preparation of core sheet] PETG (Eastman) is a non-crystalline polyester containing terephthalic acid as the acid component and ethylene glycol (about 70 mol%) and cyclohexanedimethanol (about 30 mol 0 / o) as the diol component. 100 parts by weight of Titanium Co., Ltd. was added to 100 parts by weight of Titanium Co., Ltd., and a white core sheet having a thickness of 300 / m was obtained by a T-die extrusion method.
[オーバーシートの作製] [Production of oversheet]
共重合ポリカーボネートであるレキサン S P 1 0 1 0 (二ホン ジ一ィープラ スチック社製) を用いて、 Tダイ押し出し法により厚さ 1 0 0 の透明ォー バーシートを得た。 なお、 オーバ一シートのガラス転移温度は 1 3 0 °Cである。 ただし、 ガラス転移温度は以下のように測定した。 A transparent oversheet having a thickness of 100 was obtained by a T-die extrusion method using Lexan SP101 (manufactured by Nihon Giplastic Co.), which is a copolymerized polycarbonate. The glass transition temperature of the over sheet is 130 ° C. However, the glass transition temperature was measured as follows.
ガラス転移温度の測定: Measurement of glass transition temperature:
(株) 東洋精機製作所の粘弾性スぺクトロメーターを用いて、 試料に周波数 1 H zの正弦波状に変化する歪みを加えながら、 引張弾性率の温度依存性を測定し た。 測定条件は、 試料厚み l mm、 最大歪み 1 %、 昇温速度は 4 °C/分で、 室温 からスタートした。 引張損失弾性率 E " が極大のピークを示し、 引張貯蔵弾性率 E, が大きく低下し始める付近の温度をガラス転移温度とした。 Using a viscoelastic spectrometer of Toyo Seiki Seisaku-sho, the temperature dependence of the tensile modulus was measured while applying a sinusoidally changing strain at a frequency of 1 Hz to the sample. The measurement conditions were: sample thickness lmm, maximum strain 1%, heating rate 4 ° C / min, and started at room temperature. The temperature near the point where the tensile loss elastic modulus E "shows a maximum peak and the tensile storage elastic modulus E, starts to decrease significantly is defined as the glass transition temperature.
[評価用カードサンプルの作製] [Production of evaluation card sample]
得られたコアシートに線径 0 . 1 5 mmの銅線を 4周回した 4回卷アンテナ用 ループコイルおよび縦横 5 mm X 5 mmの大きさで、 厚さ 0 . 3 5 mmの I C チップ等を等間隔で配置し、 シァノアクリレート系瞬間接着剤で仮止めして、 I Cチップ等を間に挟むようにコアシートを重ねた。 A loop coil for a four-turn antenna in which a copper wire having a wire diameter of 0.15 mm is wound around the obtained core sheet four times, and an IC chip having a size of 5 mm X 5 mm and a thickness of 0.35 mm, etc. Were arranged at equal intervals, temporarily fixed with a cyanoacrylate-based instant adhesive, and a core sheet was stacked so as to sandwich an IC chip and the like.
オーバーシート、 I Cチップ等を仮止めしたコアシート、 コアシート、 および オーバ一シ一トをこの順で重ねて、 外側のオーバーシートをそれぞれ表面が鏡面 であるクロムメツキ鋼板で挟んだ。 次いで、 プレス温度 1 3 0 °C、 試料圧力 1 5 k g f Z c m2で 1 0分間ラミネートした後、 室温まで冷却し、 カード形状に打ち 抜き評価用カードサンプルを得た。 実例 IV— 2 The oversheet, the core sheet to which the IC chip, etc. were temporarily fixed, the core sheet, and the oversheet were stacked in this order, and the outer oversheet was sandwiched between chrome plated steel plates each having a mirror-finished surface. Next, after laminating at a press temperature of 130 ° C. and a sample pressure of 15 kgf Z cm 2 for 10 minutes, the laminate was cooled to room temperature, and punched into a card shape to obtain a card sample for evaluation. Example IV—2
実例 IV— 1において、 オーバ一シ一トをポリカーボネートであるノバレックス 7 0 2 2 (三菱エンジニアリングプラスチック社製) 1 0 0重量部に対して、 可 塑剤 T C P (トリクレジルフォスフヱート、 大八化学社製) を 5重量部添加した 混合物からなるオーバ一シートに代えた以外は実例 IV— 1と同様にして、 評価用 カードサンプルを作製した。 なお、 オーバーシートのガラス転移温度は 1 3 5 °C
であった。 実例 IV— 3 In Example IV-1, the oversheet was added to 100 parts by weight of Novalex polycarbonate (manufactured by Mitsubishi Engineering-Plastics Corporation) 100 parts by weight with plasticizer TCP (tricresyl phosphate, A card sample for evaluation was prepared in the same manner as in Example IV-1, except that an oversheet consisting of a mixture to which 5 parts by weight of Daihachi Chemical Co., Ltd.) was added was used. The glass transition temperature of the oversheet is 135 ° C Met. Example IV—3
実例 IV— 2において、 オーバーシートに用いる可塑剤 T C Pの添加量を 1 8重 量部に変更した以外は実例 IV— 2と同様にして評価用力一ドサンプルを作製し た。 なお、 オーバーシートのガラス転移温度は 9 0 °Cであった。 対照 IV— 1 In Example IV-2, an evaluation force sample was prepared in the same manner as in Example IV-2, except that the amount of the plasticizer TCP used for the oversheet was changed to 18 parts by weight. The glass transition temperature of the oversheet was 90 ° C. Control IV—1
実例 IV— 1において、 オーバーシートをノバレックス 7 0 2 2からなるォー パーシートに代えた以外は実例 IV— 1と同様にして評価用カードサンプルを作製 した。 なお、 オーバーシートのガラス転移温度は 1 5 5 °Cであった。 対照 IV— 2 An evaluation card sample was prepared in the same manner as in Example IV-1, except that in Example IV-1, the oversheet was replaced with an oversheet made of NOVAREX 720-2. The glass transition temperature of the oversheet was 155 ° C. Control IV—2
実例 IV— 2において、 オーバーシートに用いる可塑剤 T C Pの添加量を 2 5重 量部に変更した以外は、 実例 IV— 2と同様にして評価用力一ドサンプルを作製し た。 なお、 オーバーシ一トのガラス転移温度は 8 0 °Cであった。 実例 IV— 1〜IV— 3、 対照 IV— 1〜! V— 2において得られた評価用カードサン プルについて、 以下の評価を行った。 In Example IV-2, an evaluation force sample was prepared in the same manner as in Example IV-2, except that the amount of the plasticizer TCP used for the oversheet was changed to 25 parts by weight. The glass transition temperature of the oversheet was 80 ° C. Examples IV—1 to IV—3, Control IV—1 to! The following evaluation was performed on the evaluation card sample obtained in V-2.
[評価] [Evaluation]
以下に示す耐熱性試験および力一ド剥離試験を行った。 The following heat resistance test and force peel test were performed.
耐熱性試験: Heat resistance test:
以下のようにして評価用カードサンプルに生じる 「そり」 を測定した。 所定温 度のオーブン中に評価用カードサンプルを入れ、 2 4時間放置した後取り出し、 室温まで冷やした評価用カードサンプルを水平板上に置き、 水平板から評価用 カードサンプル表面までの最大距離 (カードサンプルの厚みを含む) を測定す る。 オーブンの設定温度は 5 0 °Cから 5 °Cごとに高く していき、 測定値が 2 m m を越えない最高温度を 「耐熱温度」 とした。 The “warpage” generated in the evaluation card sample was measured as follows. Place the evaluation card sample in an oven at a predetermined temperature, leave it for 24 hours, remove it, place the evaluation card sample cooled to room temperature on a horizontal plate, and set the maximum distance from the horizontal plate to the evaluation card sample surface ( (Including the thickness of the card sample). The set temperature of the oven was increased every 50 ° C from 50 ° C, and the maximum temperature at which the measured value did not exceed 2 mm was defined as the “heat-resistant temperature”.
カード剥離試験: Card peel test:
評価用カードサンプルを 1 5 0 °Cの流動パラフィン中に 5分間浸漬した後、 取 り出して評価用カードサンプルの周辺部の断面を目視観察した。 After the evaluation card sample was immersed in liquid paraffin at 150 ° C. for 5 minutes, it was taken out and the cross section of the peripheral portion of the evaluation card sample was visually observed.
カード剥離試験の結果、 ガラス転移温度が 1 4 0 °C以下である実例 IV— 1〜IV 一 3および対照 IV— 2で得られた評価用力一ドサンプルは剥離が見られなかった
if、 ガラス転移温度が 1 4 0 °C以下である対照 IV— 1で得られた評価用力一ドサ ンプルは剥離が見られた。 As a result of the card peeling test, no peeling was observed in the evaluation force samples obtained in Examples IV-1 to IV-13 and Control IV-2 in which the glass transition temperature was 140 ° C or lower. If, the evaluation force sample obtained in Control IV-1 with a glass transition temperature of 140 ° C or lower showed peeling.
また、 耐熱性試験により、 ガラス転移温度が 9 0 °C以上である実例 IV— 1、 IV - 2の耐熱温度は 8 0 °Cであり、 実例 IV— 3は 7 0 となり、 ともに 7 0 °C以上 であるが、 ガラス転移温度が 9 0 °C未満である対照 IV— 2の耐熱温度は 6 0でで あった。 すなわち、 実例 IV— 1〜IV— 3の耐熱温度は実用レベル以上であるが、 対照 IV— 2は実用レベル以下である。 According to the heat resistance test, the heat resistance temperature of Examples IV-1 and IV-2 whose glass transition temperature is 90 ° C or more is 80 ° C, and that of Example IV-3 is 70 °, both of which are 70 ° C. The heat resistance temperature of Control IV-2, which is not less than C but has a glass transition temperature of less than 90 ° C, was 60. That is, the heat resistance temperature of Examples IV-1 to IV-3 is higher than the practical level, while that of Control IV-2 is lower than the practical level.
以上述べたように、 実施例 IV— 1〜! V— 3はカード剥離試験および耐熱性試験 ともに優れた結果を得た。 実例 IV— 4 As described above, Embodiment IV-1! V-3 obtained excellent results in both the card peeling test and the heat resistance test. Example IV—4
実例 IV— 1において、 コアシートとして非結晶性ポリエステル (P E T G 6 7 6 3 ) 1 0 0重量部に対して酸化チタンを 1 0重量部、 ラルリルベンゼンスルホ ン酸ナトリウムを 0 . 5重量部、 分子量約 3 0 0 0のポリエチレングリコールを 0 . 5重量部添加したものを用い、 コアシートより若干サイズの小さいオーバー シートを用いてラミネートした以夕 は実例 IV— 1と同様にして、 評価用カードサ ンプルを得た。 In Example IV-1, 100 parts by weight of titanium oxide, 0.5 parts by weight of sodium ruralylbenzenesulfonate, and 100 parts by weight of the amorphous polyester (PETG6673) were used as the core sheet. After the addition of 0.5 parts by weight of polyethylene glycol having a molecular weight of about 300, and lamination using an oversheet having a size slightly smaller than the core sheet, the same procedure as in Example IV-1 was repeated. Got a sample.
ラミネート後、 冷却してから評価用カードサンプルを取り出すとき、 メツキ板 との剥離性力 ?非常に軽く、 得られたカードの外観、 耐熱性も実例 IV— 1と同様、 優れたものであった。 以上詳しく説明したように、 実質的に非結晶性のポリエステル系樹脂に、 ポリ エチレングリコールとアルキルベンゼンスルホン酸ナトリウムとを重量比で 1 Z 9〜 9 / 1の割合で混合したものを添加量が 0 . 1重量%〜 1 . 5重量%の範囲 で添加したカード用樹脂組成物は、 ラミネート後のプレス板からの剥離性に優 れ、 かつ、 透明性、 印刷適性にも優れ、 磁気ストライプカードや I Cカードの素 材として好適に使用できるものであることが分かつた。 After lamination, when taking out an evaluation card sample was cooled, peelability force between plated plate? Very light, the appearance of the resultant card, similar to the heat resistance illustrative IV- 1, was excellent . As described in detail above, a mixture of a substantially non-crystalline polyester resin and a mixture of polyethylene glycol and sodium alkylbenzene sulfonate at a weight ratio of 1Z9 to 9/1 is added in an amount of 0. The resin composition for cards added in the range of 1% by weight to 1.5% by weight has excellent releasability from the press plate after lamination, and also has excellent transparency and printability. It has been found that it can be suitably used as an IC card material.
また、 実質的に非結晶性ポリエステル系樹脂に、 平均粒径が 5 ^ 111以下である 粉末ケィ酸および Zまたは粉末状マグネシゥムシリケートを非結晶性ポリエステ ル系樹脂 1 0 0重量%に対して 0 . 5〜 5 . 0重量%含有する樹脂組成物は、 透 明性に優れ、 カードの刻印部分に文字割れが生じず、 打ち抜き断面がフラッ トで あり、 手触りが良好で、 カードリーダ一への出し入れの際に断面が機械にひっか ることもない。
さらにまた、 実質的に非結晶性であるポリエステル系樹脂に、 平均粒径が 3 〜 1 0 mの、 粒状およひ 7または板^!犬の無機フイラ一を該非結晶性ポリエステル 系樹脂 1 0 0重量%に対して 0 . 5〜 5 . 0重量%含有する樹脂組成物は、 刻印 部分の文字割れが生じることなく、 エンボスカールも小さいので、 リーダライタ への出し入れの際に、 カードが機械に引つかかることもない。 In addition, the powdered Ca-acid and Z or powdered magnesium silicate having an average particle size of 5 ^ 111 or less were added to the substantially non-crystalline polyester resin with respect to 100% by weight of the non-crystalline polyester resin. The resin composition containing 0.5 to 5.0% by weight has excellent transparency, does not cause character cracks in the engraved portion of the card, has a flat punched cross section, has a good feel, and has a good card reader. The cross section does not catch on the machine when moving in and out. Furthermore, a substantially non-crystalline polyester-based resin, having a mean particle size of 3 to 10 m, and a granular and / or platen! The resin composition containing 0.5 to 5.0% by weight of the inorganic polyester resin of dog with respect to 100% by weight of the non-crystalline polyester resin has a small embossed curl without character breakage at the engraved portion. Therefore, the card does not catch on the machine when inserting or removing the card from the reader / writer.
また、 コアシートが非結晶性ポリエステル樹脂からなるシートであり、 ォー バーシートはガラス転移温度が 9 0〜 1 4 0 °Cであるシートからなるプラスチッ クカードは、 オーバーシートとの剥離を起こすことなく、 カードのそりを解決で きる。
The core sheet is a sheet made of an amorphous polyester resin, and the oversheet is a plastic card made of a sheet with a glass transition temperature of 90 to 140 ° C. And solve card warpage.
Claims
1 . 実質的に非結晶性のポリエステル系樹脂を主成分とすることを特徴とする 力一ド用樹脂組成物。 1. A resin composition for forceps comprising a substantially non-crystalline polyester resin as a main component.
2 . プラスチックカードの素材に用いられる材料であって、 実質的に非結晶性 のポリエステル系樹脂に、 ポリエチレングリコールとアルキルベンゼンスルホン 酸ナトリウムとを重量比で 1 Z 9〜 9 Z 1の割合で混合したものを、 0 . 1重 量%〜 1 . 5重量%の範囲で添加したことを特徴とする請求の範囲第 1項に記載 のカード用樹脂組成物。 2. A material used as a material for plastic cards, in which polyethylene glycol and sodium alkylbenzene sulfonate are mixed in a weight ratio of 1Z9 to 9Z1 to a substantially non-crystalline polyester resin. 2. The card resin composition according to claim 1, wherein said resin composition is added in a range of 0.1% by weight to 1.5% by weight.
3 . 実質的に非結晶性のポリエステル系樹脂に、 平均粒径が 5 μ m以下の粉末 状ケィ酸および粉末状マグネシウムシリケートの少なくとも 1つを、 前記実質的 に非結晶性のポリエステル系樹脂に対して 0 . 5〜5 . 0重量%の範囲で含有す ることを特徴とする請求の範囲第 1項または第 2項に記載のカード用樹脂組成 物。 3. At least one of a powdered caic acid and a powdered magnesium silicate having an average particle size of 5 μm or less is added to the substantially non-crystalline polyester resin to the substantially non-crystalline polyester resin. 3. The card resin composition according to claim 1, wherein said resin composition is contained in a range of 0.5 to 5.0% by weight.
4 . 実質的に非結晶性のポリエステル系樹脂に、 平均粒径が 3〜 1 0 μ mの粒 状または板状の無機フィラーを、 前記実質的に非結晶性のポリエステル系樹脂に 対して 2〜 1 0重量%の範囲で含有することを特徴とする請求の範囲第 1項また は第 2項に記載のカード用樹脂組成物。 4. Add a granular or plate-like inorganic filler having an average particle size of 3 to 10 μm to the substantially non-crystalline polyester-based resin. The card resin composition according to claim 1 or 2, wherein the resin composition is contained in an amount of from 10 to 10% by weight.
5 . 実質的に非結晶性のポリエステル系樹脂に、 平均粒径が 3〜 1 0 mの粒 状および板状の無機フイラ一を、 前記実質的に非結晶性のポリエステル系樹脂に 対して 2〜 1 0重量%の範囲で含有することを特徴とする請求の範囲第 1項また は第 2項に記載のカード用樹脂組成物。 5. Into the substantially non-crystalline polyester resin, a granular or plate-like inorganic filler having an average particle size of 3 to 10 m is added to the substantially non-crystalline polyester resin. The card resin composition according to claim 1 or 2, wherein the resin composition is contained in an amount of from 10 to 10% by weight.
6 . 前記非結晶性のポリエステル系樹脂が、 テレフタル酸とエチレングリコー ルと 1, 4ーシクロへキサンジメタノールとの混合物を脱水縮合させたポリエス テル系樹脂であることを特徴とする請求の範囲第 1項から第 5項のいずれかに記 載のカード用樹脂組成物。 6. The non-crystalline polyester resin is a polyester resin obtained by dehydrating and condensing a mixture of terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol. A resin composition for a card according to any one of Items 1 to 5.
7 . 請求の範囲第 2項〜第 6項に記載のいずれかのカード用樹脂組成物からな
ることを特徴とするシ一ト。 7. The card resin composition according to any one of claims 2 to 6. A sheet characterized by the following.
8 . 請求の範囲第 2項〜第 6項に記載のいずれかのカード用樹脂組成物からな る層を含むことを特徴とする力一ド。 8. A force plate comprising a layer comprising the resin composition for a card according to any one of claims 2 to 6.
9 . 前記カード用樹脂組成物が、 実質的に非結晶性のポリエステル系樹脂に、 ポリエチレングリコールとアルキルベンゼンスルホン酸ナトリゥムとを重量比で9. The resin composition for a card comprises a substantially non-crystalline polyester resin, polyethylene glycol and sodium alkyl benzene sulfonate in a weight ratio.
1 Z 9〜 9 / 1の割合で混合したものを、 0 . 1重量%〜 1 . 5重量%の範囲で 添加した樹脂組成物であり、 該樹脂組成物からなる層を 2層含むことを特徴とす る請求の範囲第 8項に記載のカード。 1 Z is a resin composition in which a mixture of 9 to 9/1 is added in a range of 0.1% by weight to 1.5% by weight, and two layers of the resin composition are included. The card according to claim 8, which is characterized by the features.
1 0 . 最夕層であるオーバーシートと内層であるコアシートを有するカードに おいて、 前記コアシートは実質的に非結晶性のポリエステル系樹脂からなり、 前 記オーバーシートはガラス転移温度が 9 0〜 1 4 0 °Cである樹脂組成物からなる ことを特徴とするカード。 10. In a card having an oversheet as an outermost layer and a core sheet as an inner layer, the core sheet is substantially made of an amorphous polyester resin, and the oversheet has a glass transition temperature of 9. A card comprising a resin composition having a temperature of 0 to 140 ° C.
1 1 . 前記オーバーシートがポリカーボネ一ト系樹脂からなることを特徴とす る請求の範囲第 1 0項に記載のカード。 11. The card according to claim 10, wherein the oversheet is made of a polycarbonate-based resin.
1 2 . 前記非結晶性のポリエステル系樹脂が、 テレフタル酸とエチレングリ コールと 1, 4ーシクロへキサンジメタノールとの混合物を脱水縮合したポリエ ステル系樹脂であることを特徴とする請求の範囲第 1 0項または第 1 1項のいず れかに記載のカード。
12. The non-crystalline polyester resin is a polyester resin obtained by dehydrating and condensing a mixture of terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol. A card according to either paragraph 10 or paragraph 11.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000509772A JP3628256B2 (en) | 1997-08-19 | 1998-06-09 | Resin composition for card, sheet and card |
AU75529/98A AU7552998A (en) | 1997-08-19 | 1998-06-09 | Resin composition for cards, and sheets and cards |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22238797 | 1997-08-19 | ||
JP9/222387 | 1997-08-19 | ||
JP31824997 | 1997-11-19 | ||
JP9/318248 | 1997-11-19 | ||
JP31824897 | 1997-11-19 | ||
JP9/318249 | 1997-11-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1999009102A1 true WO1999009102A1 (en) | 1999-02-25 |
Family
ID=27330662
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1998/002545 WO1999009102A1 (en) | 1997-08-19 | 1998-06-09 | Resin composition for cards, and sheets and cards |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP3628256B2 (en) |
AU (1) | AU7552998A (en) |
TW (1) | TW426702B (en) |
WO (1) | WO1999009102A1 (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1047723A1 (en) * | 1998-01-21 | 2000-11-02 | Eastman Chemical Company | Modified polyester with improved processability and adhesion in extrusion coating applications |
JP2001129935A (en) * | 1999-11-08 | 2001-05-15 | Dainippon Printing Co Ltd | Plastic sheet base material for card and plastic card |
JP2001151996A (en) * | 1999-11-25 | 2001-06-05 | Okamoto Ind Inc | Soft polyester based resin composition and film produced therefrom |
JP2002067554A (en) * | 2000-08-24 | 2002-03-08 | Dainippon Printing Co Ltd | Plastic card |
JP2002309068A (en) * | 2001-04-17 | 2002-10-23 | Dainippon Printing Co Ltd | Material for card and evaluation thereof |
JP2003044822A (en) * | 2001-08-03 | 2003-02-14 | Toppan Printing Co Ltd | Card |
JP2003058849A (en) * | 2001-08-10 | 2003-02-28 | Hitachi Chem Co Ltd | Ic card |
JP2009040052A (en) * | 2008-08-26 | 2009-02-26 | Mitsubishi Plastics Inc | Sheet for card, and card manufactured using the same |
FR2944024A1 (en) * | 2009-04-01 | 2010-10-08 | Cgl Pack Service | Thermoformable sheet material comprises amorphous polyethylene terephthalate and talc, and a mineral colorant, where the talc is present in the form of grains having a size of specified range |
WO2011145589A1 (en) * | 2010-05-19 | 2011-11-24 | 三菱化学株式会社 | Sheet for cards and card |
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JP2001129935A (en) * | 1999-11-08 | 2001-05-15 | Dainippon Printing Co Ltd | Plastic sheet base material for card and plastic card |
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Also Published As
Publication number | Publication date |
---|---|
TW426702B (en) | 2001-03-21 |
JP3628256B2 (en) | 2005-03-09 |
AU7552998A (en) | 1999-03-08 |
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