JPH03366Y2 - - Google Patents
Info
- Publication number
- JPH03366Y2 JPH03366Y2 JP1985057448U JP5744885U JPH03366Y2 JP H03366 Y2 JPH03366 Y2 JP H03366Y2 JP 1985057448 U JP1985057448 U JP 1985057448U JP 5744885 U JP5744885 U JP 5744885U JP H03366 Y2 JPH03366 Y2 JP H03366Y2
- Authority
- JP
- Japan
- Prior art keywords
- film
- nameplate
- ethylene
- layer
- polyethylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- -1 polypropylene Polymers 0.000 claims description 35
- 239000004743 Polypropylene Substances 0.000 claims description 19
- 229920001155 polypropylene Polymers 0.000 claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- 229920001577 copolymer Polymers 0.000 claims description 16
- 239000004698 Polyethylene Substances 0.000 claims description 14
- 229920000573 polyethylene Polymers 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 11
- 239000005977 Ethylene Substances 0.000 claims description 11
- 229920001187 thermosetting polymer Polymers 0.000 claims description 10
- 239000000853 adhesive Substances 0.000 claims description 9
- 230000001070 adhesive effect Effects 0.000 claims description 9
- 238000007639 printing Methods 0.000 claims description 8
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 5
- 239000010410 layer Substances 0.000 description 29
- 238000002844 melting Methods 0.000 description 15
- 230000008018 melting Effects 0.000 description 15
- 239000007789 gas Substances 0.000 description 12
- 230000004927 fusion Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 230000008961 swelling Effects 0.000 description 8
- 238000007740 vapor deposition Methods 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 230000007423 decrease Effects 0.000 description 5
- 230000032798 delamination Effects 0.000 description 5
- 238000013213 extrapolation Methods 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000003851 corona treatment Methods 0.000 description 3
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920005676 ethylene-propylene block copolymer Polymers 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- 229920011250 Polypropylene Block Copolymer Polymers 0.000 description 1
- 238000003854 Surface Print Methods 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000003484 crystal nucleating agent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Physical Vapour Deposition (AREA)
Description
ãèæ¡ã®è©³çŽ°ãªèª¬æã
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éæ¿ã«é¢ããã[Detailed description of the invention] [Technical field of the invention] The invention relates to nameplates for thermosetting resin molded products.
In particular, it relates to a name plate for a circuit breaker with an overcurrent protection device made of phenolic resin or polyester resin.
åŸæ¥ããã¬ãŒã«ãŒçšéæ¿ãšããŠã¯ãã¢ã«ãèžç
ããªãšã¹ãã«ãã€ã«ã ã䜿çšãããŠããã
Conventionally, aluminum vapor-deposited polyester film has been used as nameplates for breakers.
ããããªãããç±ç¡¬åæ§æš¹èãäŸãã°ããšããŒ
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éŠæç³»ã®ã¬ã¹ãçºçããã®ã§ãããªãšã¹ãã«ç³»ã®
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ãŒã«ãŒããçºçããã¬ã¹ããã¬ãŒã«ãŒè¡šé¢ãšéæ¿
ãšã®éã«æºããéæ¿ãã¬ã¹å§ã§è¹ããããå¥ãã
ãçã®æ¬ ç¹ããã€ãã However, thermosetting resins such as phenolic resins emit ammonia, formalin gas, water vapor, etc., while polyester resins emit aromatic gases, so a polyester nameplate is attached to the breaker. Then, the gas generated from the breaker would accumulate between the breaker surface and the nameplate, causing problems such as the nameplate swelling or peeling off due to the gas pressure.
ããã§ãããã«ä»£ãéæ¿ãšããŠãããªãšã¹ãã«
ãã€ã«ã ã®éå±èžçããé¢ã«å€å質éšæãäŸãã°
çŽãæ¥åãããã®çŽé¢ã«æ¥çå€ãå¡åžããŠãã¬ãŒ
ã«ãŒã«è²Œä»ããããã«ãããã®ãææ¡ãããŠãã
ïŒå®éæ56â32357å·ïŒããã®éæ¿ã§ã¯ãç±ç¡¬åæ§
æš¹èããçºçããäžèšã¬ã¹ãçŽé¢ãä»ããŠæšªæ¹å
ã«éãããšã«ãã€ãŠåŸæ¥ã®æ¬ ç¹ã解æ¶ã§ãããšã
ãŠããã Therefore, an alternative nameplate has been proposed in which a porous material, such as paper, is bonded to the metal-deposited surface of a polyester film, and an adhesive is applied to this paper surface to attach it to the breaker. Utility Model Publication No. 56-32357), this nameplate states that the drawbacks of the prior art can be overcome by allowing the gas generated from the thermosetting resin to escape laterally through the paper surface.
ããããªããããããéæ¿ã§ã¯ãå±€éæ¥çåã
å£ãã貌ãä»ããéæ¿ãå¥é¢ãããšãä»åšããçŽ
ãè£ããå床ã®äœ¿çšãäžå¯èœã«ãªãæ¬ ç¹ããã€
ãã However, such nameplates have the disadvantage that interlayer adhesive strength is poor, and when the attached nameplate is peeled off, the intervening paper is torn, making it impossible to use it again.
ãŸããç±ç¡¬åæ§æš¹èããçºçããã¬ã¹ã¯ãçŽå±€
ãä»ããŠæšªæ¹åã«æåºãããã®ã§ãæåºçµè·¯ãé·
ããªããåŸã€ãŠããã°ãã°éæ¿ãè¹ããã ããå¥
é¢ããåé¡ç¹ããªãæ®åããŠããã In addition, the gas generated from the thermosetting resin is exhausted laterally through the paper layer, resulting in a long exhaust path, and therefore the problem of nameplate swelling and peeling still remains. Ta.
ç¹ã«å€§åã®éæ¿ã§ã¯ãçŽãä»ããŠæšªæ¹åã«ã¬ã¹
ãæŸåºããæ¬ ç¹ã匷ãçŸããåŸã€ãŠå€§åã®éæ¿ã«
çŽãä»åšãããããšã¯äžå¯èœã§ãã€ãã Particularly in large nameplates, the drawback of lateral gas release through the paper becomes more apparent, and it has therefore been impossible to interpose paper in large nameplates.
æ¬èæ¡ã¯ãäžèšåŸæ¥ã®æ¬ ç¹ã解æ¶ããç±ç¡¬åæ§
æš¹èããçºçããã¬ã¹ããéæ¿ã®åãæ¹åã«æåº
ããŠéæ¿ã®è¹ãã¿ãå¥ãããé²æ¢ããããšãã§
ãããã€å±€éå¥é¢ãçããªãéæ¿ãæäŸããããš
ãç®çãšãããã®ã§ããã
The present invention solves the above-mentioned conventional drawbacks, and can prevent the nameplate from swelling and peeling by discharging the gas generated from the thermosetting resin in the thickness direction of the nameplate, and also prevents delamination. The purpose is to provide a nameplate that is not available.
äžèšç®çãéæããæ¬èæ¡ã¯ãïŒè»žå»¶äŒžããªã
ããã¬ã³ãã€ã«ã ãšã該ãã€ã«ã ã®å°ãªããš
ãçé¢ã«ç©å±€ããããšãã¬ã³âãããã¬ã³å
±éå
äœãã€ã«ã ãŸãã¯ããªãšãã¬ã³ãã€ã«ã ãšã
ããªããåèšãã€ã«ã ã®è¡šé¢ã«å°å·å±€ãæãã
ãã€ã«ã ãŸãã¯ãã€ã«ã ã®è¡šé¢ã«100ã1000
â«ã®åãã§éå±èžçå±€ã圢æããã該éå±èžçå±€
äžã«æ¥çå€ãå¡åžãããŠããããšãç¹åŸŽãšããã
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The present invention to achieve the above object consists of a biaxially stretched polypropylene film A, and an ethylene-propylene copolymer film B or a polyethylene film C laminated on at least one side of the film A, and the surface of the film A is printed. has a layer,
100 to 1000 on the surface of film B or film C
It is characterized in that a metal vapor deposited layer is formed with a thickness of 1.5 Ã
, and an adhesive is applied on the metal vapor deposited layer.
以äžãæ¬èæ¡ãå³é¢ã«ããšãã説æããã Hereinafter, the present invention will be explained based on the drawings.
第ïŒå³ã«ãããŠãïŒã¯ãã¬ãŒã«ãŒã瀺ããç±ç¡¬
åæ§æš¹èãäŸãã°ããšããŒã«ç³»æš¹èããŸãã¯ããª
ãšã¹ãã«æš¹èã§è£œé ãããŠããã In FIG. 1, numeral 1 indicates a breaker, which is made of thermosetting resin, such as phenolic resin or polyester resin.
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瀺ãããŠããã A nameplate 2 is pasted on the breaker 1, on which rating information indicating the contents of the breaker, etc. are shown.
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ããªãããã¬ã³ãã€ã«ã ïŒã®å°ãªããšãçé¢ã«
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é¢ã«å°å·ïŒãæœãããŠããã FIG. 2 shows a first embodiment of the nameplate 2, in which an ethylene-propylene copolymer film B4 is laminated on at least one side of a biaxially stretched polypropylene film A3, a metal vapor deposited layer 5 is provided on the film B4, and an adhesive layer 5 is provided on the film B4. The agent 6 is applied, and the printing 8 is applied to the surface of the film A3.
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ããªãããã¬ã³ãã€ã«ã ïŒã®å°ãªããšãçé¢ã«
ããªãšãã¬ã³ãã€ã«ã ïŒãç©å±€ãããŠãã以å€
ã¯ç¬¬ïŒå®æœäŸãšåæ§ã§ããã FIG. 3 shows a second embodiment of the nameplate 2, which is the same as the first embodiment except that a polyethylene film C7 is laminated on at least one side of a biaxially stretched polypropylene film A3.
ããã§ãæ¬èæ¡ã«ãããŠäœ¿çšãããïŒè»žå»¶äŒžã
ãªãããã¬ã³ãã€ã«ã ïŒãæ§æããããªããã
ã¬ã³ã¯ãç¹ã«éå®ããããã®ã§ã¯ãªãããéåžžã§
ã¯ã¢ã€ãœã¿ã¯ããã¯ã€ã³ããã¯ã¹IIã85ïŒ
以äžã
奜ãŸããã¯90ïŒ
以äžã§ããã230âã§ã®ã¡ã«ãã€
ã³ããã¯ã¹MIã0.1ã50gïŒ10åãç¹ã«ïŒã20gïŒ
10åã®ç¯å²ã®ãã®ã奜ãŸããã Here, the polypropylene constituting the biaxially stretched polypropylene film A3 used in the present invention is not particularly limited, but usually has an isotactic index II of 85% or more,
It is preferably 90% or more, and the melt index MI at 230°C is 0.1 to 50 g/10 minutes, especially 1 to 20 g/10 minutes.
A duration of 10 minutes is preferred.
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ã§ããããšãæãŸããã As the second component other than propylene, for example, ethylene, butene, hexene, maleic anhydride, etc. may be copolymerized in random, block or graft copolymerization, but in view of the spirit of the present invention, homopolymers are preferred.
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ã§ããã Note that polypropylene contains known additives such as crystal nucleating agents, antioxidants, heat stabilizers, slip agents, antistatic agents, antiblocking agents, fillers,
It may also contain a viscosity modifier, a coloring inhibitor, and the like.
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äœãªã©ããã¬ã³ãããŠãè¯ãã As the ethylene-propylene copolymer film B4, a film containing 50% by weight or more of ethylene-propylene copolymer, which is a polymer mainly composed of random and block copolymers, is used, and α-olefin polymers such as polyethylene and polypropylene are used. You can also blend them.
ãšãã¬ã³æåã®å«æéã¯0.5ã50ééïŒ
ã奜ãŸ
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ã¯ãšãã¬ã³âãããã¬ã³ã©ã³ãã å
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ã³ã®åèšãšãã¬ã³éãäºãã The content of the ethylene component is preferably 0.5 to 50% by weight, and in the case of a blend, the content of the ethylene component refers to the total ethylene content of the ethylene-propylene random copolymer, ethylene-propylene block copolymer, and polyethylene.
ããªãããã¬ã³ããã¬ã³ãããå Žåã50ééïŒ
ãè¶ãããšéå±èžçèã®ä»çåãäœäžã奜ãŸãã
ãªãã 50% by weight when blending polypropylene
Exceeding this is not preferable because the adhesion of the metal vapor-deposited film decreases.
ããªãšãã¬ã³ãã€ã«ã ïŒãšããŠã¯ãäœå¯åºŠã
ãªãšãã¬ã³ãé«å¯åºŠããªãšãã¬ã³ãçŽéåäœå¯åºŠ
ããªãšãã¬ã³ãªã©ã®ãã€ã«ã ãçšããããå¯åºŠã¯
0.91ã0.96ã®ç¯å²ã®ãã®ã奜ãŸããã As the polyethylene film C7, films such as low-density polyethylene, high-density polyethylene, and linear low-density polyethylene are used, and the density is
A range of 0.91 to 0.96 is preferred.
ä»ã®ããªãªã¬ãã€ã³ããã¬ã³ãããå Žåã¯ã20
ééïŒ
以äžã奜ãŸããã If blending other polyolefins, 20
It is preferably less than % by weight.
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ãã¯ããªãšãã¬ã³ãã€ã«ã ã®è¡šé¢ç²ãã¯ãè·æ¶
ãå€èŠ³ãšããã«ã¯ãRaã0.20ã1.5ÎŒmã奜ãŸã
ããé¡ç¶å
æ²¢ã®å€èŠ³ãšããã«ã¯ãRaã0.12ÎŒm以
äžã奜ãŸããã The surface roughness of the ethylene-propylene copolymer film B or polyethylene film C is preferably Ra of 0.20 to 1.5 ÎŒm in order to have a matte appearance, and Ra of 0.12 ÎŒm or less to have a mirror-like appearance. is preferred.
ãªããRaãšã¯ãäžå¿ç·å¹³åç²ãïŒã«ãããªã
å€0.25mmïŒã®ããšã§ãããJIS  060ã«ããšã
ããã®ã§ããã Note that Ra refers to center line average roughness (cutoff value 0.25 mm) and is based on JIS B 060.
Raã0.20ã1.5ÎŒmãšããã«ã¯ããšã³ãã¹æ³ãç¡
æ©ç²åãæ·»å ããæ¹æ³ãªã©ã§ãè¯ãããäžèšã«ç€º
ããšãã¬ã³âããªãããã¬ã³ãããã¯å
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䜿çšããã®ããã奜ãŸããã To adjust Ra to 0.20 to 1.5 ÎŒm, an embossing method or a method of adding inorganic particles may be used, but it is more preferable to use the ethylene-polypropylene block copolymer shown below.
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±éåäœã§ã100ã
165âã«è解ããŒã¯ã®é ç¹ãïŒç¹ä»¥äžæããã
ã®ãB. It is a block copolymer with an ethylene component of 5 to 50% by weight and the rest being propylene as the main component, and 100 to 50% by weight.
Items with three or more melting peaks at 165â.
ã ãšãã¬ã³æåïŒã50ééïŒ
ã§ä»ã¯ãããã¬ã³
ãäž»æåãšãããããã¯å
±éåäœã§ãè解ããŒ
ã¯ã126â以äžã140âæªæºã140â以äžã160â
以äžã«ïŒç¹ã¥ã€æãåã
ã®ããŒã¯ã§ã®è解ç±ïŒš
ïŒïŒïŒšïŒã
0.3âŠïŒšïŒïŒïŒïŒšïŒïŒïŒšïŒïŒâŠ0.7
ãæºè¶³ãããã®ã(b) It is a block copolymer with an ethylene component of 5 to 50% by weight and the other main component being propylene, with a melting peak of 126°C or higher and lower than 140°C, and 140°C or higher and lower than 160°C.
The heat of fusion H at each peak has one point each below.
1. H2 satisfies 0.3âŠH1/(H1+H2)âŠ0.7.
ã€ãããããã®åæã«ãããŠãããšãã¬ã³æ
åãïŒïŒïŒšïŒã®é¢ä¿ãäžèšç¯å²ããå€ãããšã
è·æ¶ãæ§ãæªåããå¹åžã«ã ã©ãçããŠå€èŠ³ãæª
ããªããéå±èžçèãšã®ä»çåãäœäžãããªã©ã®
æ¬ ç¹ãçããã If the relationship between the ethylene component, H1, and H2 is outside of the above range for either a or b,
This results in drawbacks such as poor erasability, unevenness in unevenness, poor appearance, and reduced adhesion to metal vapor deposited films.
Raã0.12ÎŒm以äžãšããã«ã¯ããšãã¬ã³æåïŒ
ã15ééïŒ
ã奜ãŸããã¯ïŒã10ééïŒ
ã®ãšãã¬ã³
âãããã¬ã³ã©ã³ãã å
±éåäœãããã¯ããªãšã
ã¬ã³ã䜿çšããã®ã奜ãŸããã To make Ra 0.12ÎŒm or less, ethylene component 1
Preferably, ~15% by weight of ethylene-propylene random copolymer or polyethylene is used, preferably 2-10% by weight.
ãšãã¬ã³âãããã¬ã³ã©ã³ãã å
±éåäœã®ãšã
ã¬ã³æåãïŒééïŒ
ã奜ãŸããã¯ïŒééïŒ
æªæºã§
ã¯éå±èžçèãšã®ä»çåãäœäžãã15ééïŒ
ã奜
ãŸããã¯10ééïŒ
ãè¶ãããšè¡šé¢å
沢床ãäœäž
ããå€èŠ³ãæªåããã If the ethylene component of the ethylene-propylene random copolymer is less than 1% by weight, preferably less than 2% by weight, the adhesion to the metal vapor deposited film will decrease, and if it exceeds 15% by weight, preferably 10% by weight, the surface gloss will decrease. and the appearance deteriorates.
ãªããé æ žå€ãæ·»å ãããªã©ããŠçµæ¶åé床ã
éãããã°ãè¡šé¢å
沢床ã¯ããã«åäžããã Incidentally, if the crystallization rate is increased by adding a nucleating agent, etc., the surface glossiness can be further improved.
ããªãšãã¬ã³ãçšããå Žåãé¡é¢ç¶å
æ²¢ãåŸã
ããããå¯åºŠã0.93ãè¶ãããšå¹³æ»æ§ã¯æªåãã
åŸåã«ããã When polyethylene is used, specular gloss can be obtained, but if the density exceeds 0.93, smoothness tends to deteriorate.
æ¬èæ¡ã«ãããŠãããªãããã¬ã³ãã€ã«ã ïŒ
ãšãã¬ã³âãããã¬ã³å
±éåäœãã€ã«ã ããŸã
ã¯äžèšããªãããã¬ã³ãã€ã«ã ïŒããªãšãã¬ã³
ãã€ã«ã ã®ïŒå±€ç©å±€ãã€ã«ã ã®åãã¯ïŒã
80ÎŒmã§ããããã€ã«ã ããã³ãã€ã«ã ã®å
ãã¯å
±ã«0.5ã10ÎŒmã§ããã In this invention, polypropylene film A/
The thickness of the ethylene-propylene copolymer film B or the two-layer laminated film of the polypropylene film A/polyethylene film C is 8 to 8.
The thickness of film B and film C are both 0.5 to 10 ÎŒm.
éå±èžçå±€ïŒãšã¯ãèžçãããéå±ã®å±€ãæ
ããéå±ã¯ç¹ã«éå®ãããªããã¢ã«ãããŠã ã奜
ãŸããããŸãèžçæ¹æ³ãç¹ã«éå®ããããé»ç±å
ç±æº¶èèžçæ³ãã€ãªã³ããŒã èžçæ³ãã¹ããã¿ãª
ã³ã°æ³ããããã¯ã€ãªã³ãã¬ãŒãã€ã³ã°æ³ãªã©ã
çšããããšãã§ããã The metal vapor deposited layer 5 refers to a vapor deposited metal layer, and the metal is not particularly limited, but aluminum is preferable. Further, the vapor deposition method is not particularly limited, and an electric heating fusion vapor deposition method, an ion beam vapor deposition method, a sputtering method, an ion plating method, or the like can be used.
ãªãç©å±€ãã€ã«ã ã®è¡šé¢ã¯ãã³ããæŸé»åŠçã
é
žåŠçãç«çœåŠççã®è¡šé¢åŠçãæœã掻æ§åãã
æ¹ãè¯ãããã®éãçªçŽ ã¬ã¹äžãããã¯çªçŽ ãã
ã³äºé
žåççŽ æ··åã¬ã¹äžã§ã³ããæŸé»åŠçããã
æ¹ã奜ãŸããã The surface of the laminated film has been subjected to corona discharge treatment,
It is better to perform surface treatment such as acid treatment or fire treatment for activation, and in this case, it is preferable to perform corona discharge treatment in nitrogen gas or a mixed gas of nitrogen and carbon dioxide.
ç²çå€ïŒã¯ç¹ã«éå®ãããªãããæå§æ¥çå€ã
å€ã䜿çšãããã The adhesive 6 is not particularly limited, but pressure-sensitive adhesives are often used.
æå§æ¥çå€ãšããŠã¯ãã¢ã¯ãªã«é
žãšã¹ãã«ç³»ã®
ãã®ãäžè¬ã«äœ¿çšãããã As the pressure sensitive adhesive, acrylic ester type adhesives are generally used.
éå±èžçå±€ïŒã®åãã¯ãéåžžã§ã¯100ã1000â«
ã§ããã奜ãŸããã¯200ã700â«ã§ããã The thickness of the metal vapor deposition layer 5 is usually 100 to 1000 Ã
.
and preferably 200 to 700 Ã
.
ãã®åãã100â«ã奜ãŸããã¯200â«ã«æºããªã
ãšå
ç·åå°çãäœäžããéããŠèŠããããéå±å
æ²¢ãæžå°ããé»ã€ãœãå€èŠ³ãšãªã奜ãŸãããªãã If the thickness is less than 100 Ã
, preferably less than 200 Ã
, the light reflectance decreases, the film becomes transparent, the metallic luster decreases, and a blackish appearance becomes undesirable.
ãŸãã1000â«ã奜ãŸããã¯700â«ãè¶ãããšã¬
ã¹ééæ§ãæªããªããè¹ããå¥ãããªã©ãçºçã
ãã Moreover, if it exceeds 1000 Ã
, preferably 700 Ã
, gas permeability deteriorates, causing swelling, peeling, etc.
å°å·å±€ïŒã¯ãéšåå°å·ïŒæåãæš¡æ§ãªã©ïŒãå
š
é¢å°å·ã®ãããã«ããèšããããŠãè¯ããå€è²é
ãå°å·ã«ããèšããããŠãè¯ãã The printed layer 8 may be provided by either partial printing (letters, patterns, etc.) or full-surface printing, or may be provided by multicolor overlapping printing.
å°å·ãããã«çŸããèŠããããèæ©èæ§ãäžå±€
è¯ããããããå°å·å±€ã®äžã«éææš¹èãã³ãŒãã€
ã³ã°ãããããã€ã«ã ãã©ãããŒããããããŠã
è¯ãã In order to make the print look more beautiful and to improve its abrasion resistance, the print layer may be coated with a transparent resin or a film may be laminated thereon.
å°å·ã€ã³ããç¹ã«éå®ãããã®ã§ã¯ãªããã°ã©
ãã€ããªãã»ãããUVãªã©ããããã®ã€ã³ãã
䜿çšããŠãè¯ãããŸããå°å·ã€ã³ãä»çåãåäž
ãããããããã€ã«ã ã®è¡šé¢ã«ã¢ã³ã«ãŒã³ãŒã
å±€ãèšããããšãã§ããã The printing ink is not particularly limited either, and any ink such as gravure, offset, UV, etc. may be used. Furthermore, an anchor coat layer may be provided on the surface of the film A in order to improve printing ink adhesion.
æ¬èæ¡ã®éæ¿ã補é ããã«éããŠã¯ãããªãã
ãã¬ã³ãæš¹è枩床ã§320âãè¶ããªã枩床ã奜ãŸ
ããã¯200ã300âã§è解ããäžæ¹ããšãã¬ã³âã
ããã¬ã³å
±éåäœãŸãã¯ããªãšãã¬ã³ãæš¹è枩床
300âãè¶ããªã枩床ã奜ãŸããã¯200âã§è解
ããå£éããå
±æŒåºããŠå·åŽãã©ã äžã«ãã€ã¹ã
ããããšã«ãã€ãŠãç¡å»¶äŒžïŒå±€ç©å±€ãã€ã«ã ã補
é ããã In manufacturing the nameplate of the present invention, polypropylene is melted at a resin temperature not exceeding 320°C, preferably 200-300°C, while ethylene-propylene copolymer or polyethylene is melted at a resin temperature of
An unstretched two-layer laminate film is produced by melting at a temperature not exceeding 300°C, preferably 200°C, coextruding from a die and casting onto a cooling drum.
次ãã§ãã€ã¹ãããäžèšãã€ã«ã ãïŒè»žé
åã
ããŠãïŒè»žå»¶äŒžç©å±€ãã€ã«ã ãåŸãã Next, the cast film is biaxially oriented to obtain a biaxially stretched laminated film.
é
åãäžããæ¹æ³ã¯ãå
¬ç¥ã®æ¹æ³ãäŸãã°ããŒ
ã«å»¶äŒžãå§å»¶ããã³ã¿ãŒå»¶äŒžããã€ã¹ã¯å»¶äŒžãã
ã«ã延䌞ããã³ãã®çµåããªã©ãçšããããšãã§
ããã As a method for imparting orientation, known methods such as roll stretching, rolling, tenter stretching, disk stretching, belt stretching, and combinations thereof can be used.
以äžè¿°ã¹ãããã«æ¬èæ¡ã«ããã°ãïŒè»žå»¶äŒžã
ãªãããã¬ã³ãã€ã«ã ã®å°ãªããšãçé¢ã«ããš
ãã¬ã³âãããã¬ã³å
±éåäœãã€ã«ã ãŸãã¯ã
ãªãšãã¬ã³ãã€ã«ã ãç©å±€ããããã€ã«ã ã®
è¡šé¢ã«å°å·å±€ãæãããã®ãã€ã«ã ãŸãã¯ãã€
ã«ã ã®è¡šé¢ã«100ã1000â«ã®åãã§éå±èžçå±€
ã圢æããããã®éå±èžçå±€äžã«æ¥çå€ãå¡åžã
ããŠããã®ã§ãäžèšã®å¹æãå¥ããããšãã§ã
ãã
As described above, according to the present invention, the ethylene-propylene copolymer film B or the polyethylene film C is laminated on at least one side of the biaxially stretched polypropylene film A, and the surface of the film A has a printing layer. Since a metal vapor deposition layer is formed on the surface of film B or film C to a thickness of 100 to 1000 Ã
, and an adhesive is applied onto this metal vapor deposition layer, the following effects can be achieved.
〠éæ°æ§ã«å¯ãããªãããã¬ã³ãã€ã«ã ã䜿çš
ããŠããã®ã§ãç±ç¡¬åæ§æš¹èæå補åããçºç
ããã¬ã¹ã容æã«æåºããããšãã§ãããB. Since polypropylene film with high breathability is used, gas generated from thermosetting resin molded products can be easily discharged.
åŸã€ãŠãæ¬èæ¡ã®éæ¿ã¯åŸæ¥ã®ããã«è¹ãã
ã ããå¥é¢ããããšããªããé·æã«ããã€ãŠäœ¿
çšããããšãã§ããã Therefore, the nameplate of the present invention does not swell or peel off unlike conventional plates, and can be used for a long period of time.
ã æ¬èæ¡ã®éæ¿ã§ã¯ãç±ç¡¬åæ§æš¹èæå補åã
ãçºçããã¬ã¹ããéæ¿ã®åãæ¹åã«æåºãã
ããšãã§ããã(b) With the nameplate of the present invention, gas generated from the thermosetting resin molded product can be discharged in the thickness direction of the nameplate.
åŸã€ãŠãéæ¿ã®å€§å°ã«é¢ä¿ããããšããªãã
åŸæ¥ã¯ç¹ã«å¥é¢ãåé¡ã«ãªã€ã倧åã®éæ¿ã補
é ããããšãã§ããã Therefore, it is not related to the size of the nameplate,
It is possible to manufacture large nameplates, for which peeling has traditionally been a problem.
ã éå±èžçå±€ããšãã¬ã³âãããã¬ã³å
±éåäœ
ãŸãã¯ããªãšãã¬ã³ã«åœ¢æãããŠããã®ã§ãä»
çåã匷ããæ¬èæ¡ã®éæ¿ãç±ç¡¬åæ§æš¹èæå
åããå¥é¢ããŠãå±€éå¥é¢ãçããããšããª
ãã容æã«å䜿çšããããšãã§ãããC. Since the metal vapor deposition layer is formed of ethylene-propylene copolymer or polyethylene, it has strong adhesion, and even when the nameplate of the present invention is peeled off from a thermosetting resin molded product, delamination does not occur and it is easy to do so. can be reused.
ãªããæ¬èæ¡ã§äœ¿çšããçšèªã®èª¬æãäžèšã«è¿°
ã¹ãã Note that the terms used in the present invention will be explained below.
(1) ã¢ã€ãœã¿ã¯ããã¯ã€ã³ããã¯ã¹II
è©Šæã®ãã€ã«ã ïŒWmgïŒãçŽïŒcmå¹³æ¹ã®å€§ã
ãã«åããããããœãã¯ã¹ã¬ãŒæœåºåšã«å
¥ãã沞
éš°ïœâããã¿ã³ã§12æéæœåºããã(1) Isotactic Index II A sample film (Wmg) is cut into approximately 1 cm square pieces, placed in a Soxhlet extractor, and extracted with boiling n-heptane for 12 hours.
次ãã§ããã®è©Šæãåãåºãã80âã100mmHg
ã§ïŒæéç空也ç¥ããåŸãééã枬å®ããã Next, take out this sample and heat it at 80â and 100mmHg.
After vacuum drying for 2 hours, the weight is measured.
ãã®ééãWâ²ïŒmgïŒãšãããšãã¢ã€ãœã¿ã¯ã
ãã¯ã€ã³ããã¯ã¹ã¯ã次åŒã§æ±ããããã If its weight is W' (mg), the isotactic index is calculated by the following formula.
ã¢ã€ãœã¿ã¯ããã¯ã€ã³ããã¯ã¹ïŒïŒ
ïŒ
ïŒ100ÃWâ²ïŒïŒ·
(2) ã¡ã«ãã€ã³ããã¯ã¹MI
ASTM â1238â57Tã«åŸã€ãŠ230âã§æž¬å®
ããã Isotactic Index (%) = 100 x W'/W (2) Melt Index MI Measured at 230°C according to ASTM D-1238-57T.
(3) è解ããŒã¯ã®é ç¹
PerkinâElmer瀟補瀺差走æ»ç±éèšModel
DSCâïŒåãçšãã5mgã®è©Šæã20âïŒåã®ææž©
é床ã§280âãŸã§ææž©ãïŒåä¿æããåŸãåé床
ã§å·åŽããå床ææž©ããæã®ãããããã»ã«ã³ã
ã©ã³ã®è解æ²ç·ãåãã(3) Vertex of melting peak Perkin-Elmer differential scanning calorimeter model
So-called second-run melting occurs when a 5 mg sample is heated to 280°C at a heating rate of 20°C/min, held for 5 minutes, cooled at the same rate, and heated again using the DSC-2 model. Take a curve.
(4) èè§£ç± ç¬¬ïŒå³ã第ïŒå³ã«äŸã瀺ãã(4) Heat of fusion Examples are shown in FIGS. 4 and 5.
è解ããŒã¯ã®ãã¡ãäœæž©åŽã®è解ããŒã¯ã
ïŒãé«æž©åŽã®è解ããŒã¯ãïŒãšããããŸãã
åã
ã®è解ããŒã¯ã®é ç¹ãããªãã¡ããŒã¯ã®æ¥µå°
ç¹ãïŒïŒ¢ãšãã該é ç¹ã®æž©åºŠãåã
TmïŒïŒ
TmïŒãšããã Among the melting peaks, the melting peak on the low temperature side is P
1. The melting peak on the high temperature side is P2. Also,
The apex of each melting peak, that is, the minimum point of the peak, is defined as A and B, and the temperatures at the apex are Tm1 and Tm1, respectively.
Let it be Tm2.
次ã«è解ç±ã®æ±ãæ¹ã第ïŒå³ã®ç¬¬ïŒããŒã¯ïŒ°ïŒ
ã§ç€ºãããŸãåœè©²åžåã®éå§ç¹ïŒŽïŒãšçµç¹ïŒŽïŒã
çŽç·ïŒç¬¬ïŒå³ã®ç Žç·ïŒ£ïŒã§çµã³åºç·ãšããã Next, we will explain how to calculate the heat of fusion at the first peak P1 in Figure 4.
Indicated by First, the starting point T1 and the ending point T2 of the absorption are connected by a straight line (broken line C in FIG. 4) to form a baseline.
ããŒã¯ååã®çŽç·éšåã®è£å€ç·ãšåºç·ãšã®äº€ç¹
ãïŒãããŒã¯åŸåã®çŽç·éšåã®è£å€ç·ãšåºç·ãš
ã®äº€ç¹ãïŒãšããããŒã¯ã»è£å€ç·ã»åºç·ã§å²ãŸ
ããéšåïŒæç·éšåïŒã®é¢ç©ããè解ç±ïŒšïŒãšã
ããåæ§ã«ç¬¬ïŒããŒã¯ïŒ°ïŒã§ã®è解ç±ïŒšïŒãæ±ã
ãã The intersection of the extrapolation line of the linear part in the first half of the peak and the baseline is T5, the intersection of the extrapolation line of the linear part of the latter half of the peak with the baseline is T6, and the area of the part surrounded by the peak, extrapolation line, and baseline (shaded part) is is the heat of fusion H1. Similarly, the heat of fusion H2 at the second peak P2 is determined.
ãã ãã第ïŒå³ã«ç€ºãããã«ã第ïŒããŒã¯ïŒ°ïŒ
ã®çµäºç¹ïŒŽïŒãšç¬¬ïŒããŒã¯ïŒ°ïŒã®éå§ç¹ïŒŽïŒãé
ãªããäžã€ã®ç¹ïŒ€ãšãªããïŒãšïŒŽïŒãçµã¶åºç·
ããå€ããå Žåã¯ãç¹ïŒ€ããåçŽã«äžãããåº
ç·ïŒ£ãšã®äº€ç¹ãïŒãšããŠããŒã¯åŸåïŒç¬¬ïŒããŒ
ã¯ïŒ°ïŒã®å Žåã¯ããŒã¯ååïŒã®çŽç·éšåãšïŒŽïŒã
çµã¶ç·ãè£å€ç·ãšã¿ãªããŠé¢ç©ãæ±ããã However, as shown in FIG. 5, the first peak P1
The end point T2 and the start point T3 of the second peak P2 overlap to form one point D, and if it deviates from the baseline C connecting T1 and T4, the intersection with the baseline C drawn perpendicularly from point D is set as T9. The area is determined by regarding the line connecting the second half (the first half of the peak in the case of the second peak P2) straight line portion and T9 as an extrapolation line.
以äžãæ¬èæ¡ã®å®æœäŸãè¿°ã¹ãã Examples of the present invention will be described below.
å®æœäŸ ïŒ
230âã®ã¡ã«ãã€ã³ããã¯ã¹ïŒMIïŒ1.0ãIIã95
ïŒ
ã®ããªãããã¬ã³ãšãMIã3.0ããšãã¬ã³æå
20ééïŒ
ããããã¬ã³æå80ééïŒ
ã§DSCã®è
解ããŒã¯ã®é ç¹ã124âã145âã159âã®ïŒç¹ã«
ããããã«éåãããšãã¬ã³âãããã¬ã³ããã
ã¯å
±éåäœãäºå±€å£éã§å
±æŒåºãã40âã®å·åŽã
ã©ã ã«å·»ãä»ããã·ãŒãç¶ã«æ圢ãã瞊æ¹åã«
130âã§4.5åã暪æ¹åã«155âã§10åé次äºè»žå»¶
䌞ãã160âã§ç±åºå®ããã
Example 1 Melt index (MI) 1.0 at 230°C, II 95
% polypropylene, MI 3.0, ethylene content
An ethylene-propylene block copolymer polymerized with 20% by weight and 80% by weight of propylene component so that the apex of the DSC melting peak was at three points of 124°C, 145°C, and 159°C was coextruded with a two-layer die. Wrap it around a cooling drum at â, form it into a sheet, and roll it vertically.
It was sequentially biaxially stretched 4.5 times at 130°C and 10 times in the transverse direction at 155°C, and heat set at 160°C.
次ãã§ã³ããæŸé»åŠçãæœãã50ÎŒmïŒããªãã
ãã¬ã³å±€48ÎŒmãå
±éåäœå±€2ÎŒmïŒã®ãã€ã«ã ã
åŸãããã®ãã€ã«ã è¡šé¢ã®ãã¬åŒµåã¯äž¡é¢ãšã36
ãã€ã³ïŒcmã§ãããå
±éåäœå±€ã®è¡šé¢ç²ãRaã
0.28ÎŒmã§ãåªããè·æ¶ãæ§ãæããŠããã Then, a corona discharge treatment was performed to obtain a film of 50 ÎŒm (polypropylene layer: 48 ÎŒm, copolymer layer: 2 ÎŒm). The wetting tension on the surface of this film is 36 on both sides.
dyne/cm, and the surface roughness Ra of the copolymer layer is
It had a diameter of 0.28 ÎŒm and had excellent erasing properties.
æ¬ãã€ã«ã ã®å
±éåäœå±€è¡šé¢ã«ç空èžçæ³ã§ã¢
ã«ãããŠã ãçŽ400â«èžçããå察é¢ïŒããªãã
ãã¬ã³å±€ïŒã«ã°ã©ãã€å°å·ããã Approximately 400 Ã
of aluminum was deposited on the surface of the copolymer layer of this film using a vacuum deposition method, and gravure printing was performed on the opposite side (polypropylene layer).
æŽã«ã¢ã«ãããŠã èžçé¢ã«ç²çå€ãå¡åžããæ¶
ãéå
æ²¢ãæããéæ¿ãäœæããã Furthermore, an adhesive was applied to the aluminum vapor-deposited surface to create a nameplate with an eraser luster.
以äžã®ããã«ããŠäœæããéæ¿ãé»ç£æ¥è§Šåšã®
ã¢ãŒã«ãã±ãŒã¹ïŒããšããŒã«æš¹è補ïŒã«è²Œãä»
ãã80âã95ïŒ
RHã§16æéæŸçœ®ããããéæ¿ã®
è¹ãããå¥ããçŸè±¡ã¯å
šãã¿ãããªãã€ãã The nameplate created as described above was attached to the molded case (made of phenolic resin) of the electromagnetic contactor and left at 80â and 95%RH for 16 hours, but no swelling or peeling of the nameplate was observed. Ta.
ãŸããéæ¿ãäžèšã¢ãŒã«ãã±ãŒã¹ã«å¯Ÿã貌ãä»
ããå¥é¢ãïŒåç¹°ãè¿ããããèžçå±€ãªã©ã§ã®å±€
éå¥é¢çŸè±¡ã¯ã¿ãããªãã€ãã Further, although the nameplate was pasted on the molded case and peeled off three times, no delamination phenomenon was observed in the vapor deposited layer or the like.
æ¯èŒäŸ ïŒ
å®æœäŸïŒã§åŸãããéæ¿ã®èžçé¢ãšå°å·é¢ãé
ã«ãããã®ãäœæããïŒèžçé¢âŠâŠããªãããã¬
ã³å±€ãå°å·é¢âŠâŠãšãã¬ã³âãããã¬ã³å
±éåäœ
å±€ïŒãComparative Example 1 The nameplate obtained in Example 1 was created with the vapor-deposited side and the printed side reversed (vapor-deposited side: polypropylene layer, printed side: ethylene-propylene copolymer layer).
å®æœäŸïŒãšåæ§ã«è²Œãä»ãè©Šéšãå®æœããã A pasting test was conducted in the same manner as in Example 1.
éæ¿ã«è¹ããšå¥ããçŸè±¡ã¯ã¿ãããªãã€ããã
éæ¿ãå¥é¢ãããšéå±èžçå±€âãã€ã«ã éã§å±€é
å¥é¢ãçºçããã Although no swelling or peeling was observed on the nameplate,
When the nameplate was peeled off, delamination occurred between the metal vapor deposited layer and the film.
æ¯èŒäŸ ïŒ
25ÎŒmã®ããªãšãã¬ã³ãã¬ãã¿ã¬ãŒããã€ã«ã
ãçšããŠå®æœäŸïŒãšåæ§ã«ããŠéæ¿ãäœæããã
ãã®éæ¿ãå®æœäŸïŒãšåæ§ã«è²Œãä»ãè©Šéšãå®æœ
ãããšãããè¹ããå¥ããçŸè±¡ãçºçãããComparative Example 2 A nameplate was created in the same manner as in Example 1 using a 25 ÎŒm polyethylene terephthalate film.
When this nameplate was subjected to a pasting test in the same manner as in Example 1, swelling and peeling phenomena occurred.
æ¯èŒäŸ ïŒ
25ÎŒmã®ããªãšãã¬ã³ãã¬ãã¿ã¬ãŒããã€ã«ã
ã®çé¢ã«ã¢ã«ãããŠã ã400â«ç空èžçããå察
é¢ã«ã°ã©ãã€å°å·ãæœãã次ãã§èžçé¢äžã«
20gïŒm2ã®èèçŽã貌åãããæŽã«ãã®äžã«æ¥ç
å€ãå¡åžããŠéæ¿ãäœæãããComparative Example 3 400 Ã
of aluminum was vacuum-deposited on one side of a 25 ÎŒm polyethylene terephthalate film, gravure printing was performed on the other side, and then aluminum was deposited on the other side.
A nameplate was created by laminating 20 g/m 2 tissue paper and then applying adhesive on top of it.
ãã®éæ¿ãå®æœäŸïŒãšåæ§ã«è²Œãä»ãè©Šéšãå®
æœãããšãããäžéšã«è¹ããå¥ããçŸè±¡ã確èªã§
ããã When this nameplate was subjected to a pasting test in the same manner as in Example 1, swelling and peeling phenomena were observed in some parts.
ãŸããéæ¿ãå¥é¢ãããšçŽã®éšåã§å±€éå¥é¢ã
çºçããã Furthermore, when the nameplate was peeled off, delamination occurred in the paper part.
第ïŒå³ã¯éæ¿ã貌ãä»ãããã¬ãŒã«ãŒã®æèŠ
å³ã第ïŒå³ã¯æ¬èæ¡ã®ç¬¬ïŒå®æœäŸã瀺ãæ¡å€§æé¢
å³ã第ïŒå³ã¯æ¬èæ¡ã®ç¬¬ïŒå®æœäŸã瀺ãæ¡å€§æé¢
å³ã第ïŒå³ããã³ç¬¬ïŒå³ã¯ãšãã¬ã³âãããã¬ã³
å
±éåäœã®è解æ²ç·ã®äŸã瀺ãå³ã§ããã
ïŒâŠâŠéæ¿ãïŒâŠâŠïŒè»žå»¶äŒžããªãããã¬ã³ã
ã€ã«ã ãïŒâŠâŠãšãã¬ã³âãããã¬ã³å
±éåäœã
ã€ã«ã ãïŒâŠâŠéå±èžçå±€ãïŒâŠâŠæ¥çå€å±€ãïŒ
âŠâŠããªãšãã¬ã³ãã€ã«ã ãïŒâŠâŠå°å·å±€ãïŒ
âŠâŠäœæž©åŽã®è解ããŒã¯ãïŒâŠâŠé«æž©åŽã®è解
ããŒã¯ãïŒâŠâŠäœæž©åŽè解ããŒã¯ã®è解ç±ã
ïŒâŠâŠé«æž©åŽè解ããŒã¯ã®è解ç±ã
Fig. 1 is a perspective view of a breaker with a nameplate attached, Fig. 2 is an enlarged sectional view showing the first embodiment of the invention, Fig. 3 is an enlarged sectional view showing the second embodiment of the invention, and Fig. 4 is an enlarged sectional view showing the second embodiment of the invention. 5 and 5 are diagrams showing examples of melting curves of ethylene-propylene copolymers. 2... Nameplate, 3... Biaxially stretched polypropylene film, 4... Ethylene-propylene copolymer film, 5... Metal vapor deposition layer, 6... Adhesive layer, 7
...Polyethylene film, 8...Printing layer, P1
...melting peak on the low temperature side, P2...melting peak on the high temperature side, H1...heat of fusion of the melting peak on the low temperature side, H
2...Heat of fusion at the high temperature side melting peak.
Claims (1)
ã«ã ã®å°ãªããšãçé¢ã«ç©å±€ããããšãã¬ã³â
ãããã¬ã³å ±éåäœãã€ã«ã ãŸãã¯ããªãšãã¬
ã³ãã€ã«ã ãšãããªããåèšãã€ã«ã ã®è¡šé¢
ã«å°å·å±€ãæãããã€ã«ã ãŸãã¯ãã€ã«ã ã®
è¡šé¢ã«100ã1000â«ã®åãã§éå±èžçå±€ã圢æã
ãã該éå±èžçå±€äžã«æ¥çå€ãå¡åžãããŠããã
ãšãç¹åŸŽãšããç±ç¡¬åæ§æš¹èæååçšéæ¿ã A biaxially stretched polypropylene film A, and an ethylene film laminated on at least one side of the film A.
It consists of a propylene copolymer film B or a polyethylene film C, and has a printing layer on the surface of the film A, and a metal vapor deposited layer with a thickness of 100 to 1000 Ã is formed on the surface of the film B or film C, and the metal A nameplate for thermosetting resin molded products that is characterized by having an adhesive coated on the vapor deposited layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1985057448U JPH03366Y2 (en) | 1985-04-19 | 1985-04-19 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1985057448U JPH03366Y2 (en) | 1985-04-19 | 1985-04-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61173339U JPS61173339U (en) | 1986-10-28 |
JPH03366Y2 true JPH03366Y2 (en) | 1991-01-09 |
Family
ID=30581987
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1985057448U Expired JPH03366Y2 (en) | 1985-04-19 | 1985-04-19 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03366Y2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5632357B2 (en) * | 1974-10-30 | 1981-07-27 | ||
JPS5849963A (en) * | 1982-07-21 | 1983-03-24 | Hitachi Ltd | Laser printer |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5632357U (en) * | 1979-08-21 | 1981-03-30 |
-
1985
- 1985-04-19 JP JP1985057448U patent/JPH03366Y2/ja not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5632357B2 (en) * | 1974-10-30 | 1981-07-27 | ||
JPS5849963A (en) * | 1982-07-21 | 1983-03-24 | Hitachi Ltd | Laser printer |
Also Published As
Publication number | Publication date |
---|---|
JPS61173339U (en) | 1986-10-28 |
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