AU709752B2 - Laser-markable plastic labels - Google Patents
Laser-markable plastic labels Download PDFInfo
- Publication number
- AU709752B2 AU709752B2 AU26901/95A AU2690195A AU709752B2 AU 709752 B2 AU709752 B2 AU 709752B2 AU 26901/95 A AU26901/95 A AU 26901/95A AU 2690195 A AU2690195 A AU 2690195A AU 709752 B2 AU709752 B2 AU 709752B2
- Authority
- AU
- Australia
- Prior art keywords
- laser
- label
- core layer
- opaque material
- layer
- 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.)
- Ceased
Links
- 229920003023 plastic Polymers 0.000 title claims description 24
- 239000004033 plastic Substances 0.000 title claims description 24
- 239000000463 material Substances 0.000 claims abstract description 105
- 239000012792 core layer Substances 0.000 claims abstract description 55
- 229920002457 flexible plastic Polymers 0.000 claims abstract description 24
- 239000010410 layer Substances 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 45
- 230000008569 process Effects 0.000 claims description 29
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 25
- 230000000007 visual effect Effects 0.000 claims description 22
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000004408 titanium dioxide Substances 0.000 claims description 12
- 239000000853 adhesive Substances 0.000 claims description 11
- 230000001070 adhesive effect Effects 0.000 claims description 11
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 10
- 239000010445 mica Substances 0.000 claims description 7
- 229910052618 mica group Inorganic materials 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- 229920000098 polyolefin Polymers 0.000 claims description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- 230000001678 irradiating effect Effects 0.000 claims 1
- 238000002372 labelling Methods 0.000 abstract description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 44
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 42
- 239000000047 product Substances 0.000 description 23
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 21
- -1 conditioners Substances 0.000 description 21
- 239000011162 core material Substances 0.000 description 18
- 239000012141 concentrate Substances 0.000 description 16
- 239000000203 mixture Substances 0.000 description 16
- 229920001577 copolymer Polymers 0.000 description 15
- 238000007639 printing Methods 0.000 description 15
- 238000010330 laser marking Methods 0.000 description 14
- 229920000578 graft copolymer Polymers 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 13
- 230000009467 reduction Effects 0.000 description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 229920005629 polypropylene homopolymer Polymers 0.000 description 9
- 239000004743 Polypropylene Substances 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
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- 238000001125 extrusion Methods 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
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- 239000011159 matrix material Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
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- 239000000049 pigment Substances 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
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- 230000002411 adverse Effects 0.000 description 3
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- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
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- 238000005470 impregnation Methods 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000005549 size reduction Methods 0.000 description 2
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- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000013175 Crataegus laevigata Nutrition 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003522 acrylic cement Substances 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000000882 contact lens solution Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
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- 238000010348 incorporation Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- G—PHYSICS
- G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F3/00—Labels, tag tickets, or similar identification or indication means; Seals; Postage or like stamps
- G09F3/02—Forms or constructions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/267—Marking of plastic artifacts, e.g. with laser
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65C—LABELLING OR TAGGING MACHINES, APPARATUS, OR PROCESSES
- B65C3/00—Labelling other than flat surfaces
- B65C3/06—Affixing labels to short rigid containers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65C—LABELLING OR TAGGING MACHINES, APPARATUS, OR PROCESSES
- B65C9/00—Details of labelling machines or apparatus
- B65C9/46—Applying date marks, code marks, or the like, to the label during labelling
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D23/00—Details of bottles or jars not otherwise provided for
- B65D23/08—Coverings or external coatings
- B65D23/0842—Sheets or tubes applied around the bottle with or without subsequent folding operations
- B65D23/085—Sheets or tubes applied around the bottle with or without subsequent folding operations and glued or otherwise sealed to the bottle
-
- G—PHYSICS
- G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F3/00—Labels, tag tickets, or similar identification or indication means; Seals; Postage or like stamps
- G09F3/02—Forms or constructions
- G09F2003/0201—Label sheets intended to be introduced in a printer, e.g. laser printer
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Theoretical Computer Science (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Laminated Bodies (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
- Labeling Devices (AREA)
Abstract
Flexible plastic labels which exhibit excellent ink-printability, excellent laser-imprintability and excellent mechanical properties are produced by incorporating a suitable laser-opaque material into the core layer of a multilayer coextrudate of the type previously used for labeling flexible plastic bottles.
Description
WO 95134263 PCT/US95/06258 -1- LASER-MARKABLE PLASTIC LABELS BACKGROUND OF THE INVENTION The present invention relates to flexible, plastic labels for 'use on flexible plastic bottles, which labels are both ink printable and laser-markable.
Many commodities are supplied today in squeezable, flexible plastic bottles. Examples of such materials are household cleaning products such as sink and bathtub cleaners, liquid soaps and detergents and the like as well as personal care products such as shampoos, conditioners, lotions, suntan oils and the like.
Traditionally, flexible labels for squeezable, flexible plastic bottles have been made from paper coated with pressure sensitive adhesives. More recently, plastics have replaced paper to a large extent for this purpose. Plastic labels tend to exhibit a higher degree of flexibility, squeezability and a greater resistance to water and other chemicals than paper. Accordingly, plastic labels are becoming increasingly popular for use on flexible plastic bottles.
Attaching flexible plastic labels to flexible plastic bottles is normally accomplished in one of two ways. In one way, a pressure sensitive adhesive is applied to the label and the label attached to a previously formed bottle by pressure. In the other way, known as IMFL (In Mold Film Label), the label is placed into the mold used to form the bottle by blow molding and the label incorporated physically into the plastic bottle itself as part of the blow molding operation. In this procedure, a heat-activatable adhesive is normally applied to the label for firmly bonding the label to the bottle body.
In actual industrial practice, flexible plastic labels are attached to flexible plastic bottles at high rates of speed. For example, typical industrial applications using pressure sensitive labels can process as many as 200 bottles per minute and even up to 600 bottles per minute. In typical industrial applications for IMFL, 5 to 150 bottles per minute can be made with labels attached.
An important property of flexible plastic labels is that they are ink-printable. Ink printability depends both on the physical as well as chemical nature of the label surface to be printed.
Accordingly, it is important in producing such labels that the materials and processes used to form the labels give label products having the appropriate surface properties.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTIUS9S/06258 -2- In addition to surface properties, however, it is also important that labels exhibit appropriate gross mechanical properties. In order that the labels can flex with the bottles to which they are attached, they obviously must exhibit suitable flexibility, at least in one direction (usually the transverse direction). Moreover, in order that they can be effectively used in the modern, high-speed industrial processes described above, the labels must also exhibit additional properties such as die cutability, matrix stripability, dispensability with enough stiffness to be dispensed at high speed from a peel plate or handled for insertion in a mold) and the like. Also, pressure sensitive labels further need to be repositionable, when misapplied they can be easily peeled off the bottle in a single piece with all the adhesive remaining on the label.
In order to meet these requirements, much technology has been developed for the manufacture of flexible plastic labels. In accordance with one such development, the label body is made by coextruding a number of different plastic materials together to form a multilayer coextruded product. A real advantage of this approach is that the main body of the film can be formulated to maximize the desired gross mechanical properties of the label, while the skin layers of the product can be tailored for accepting printing ink, for receiving adhesives or both.
A good description of how flexible plastic labels can be tailored to meet a variety of different physical requirements while still retaining ink-printability, both in the case of pressure sensitive adhesive labels and heat sensitive adhesive labels, can be found in U.S. 4,713,273; U.S. 4,888,075; U.S. 4,946,532; U.S. 5,143,570; U.S. 5,186,782 and U.S. 5,242,650, the disclosures of which are incorporated herein by reference.
One type of product that is often sold in flexible plastic bottles is pharmaceuticals such as contact lens solutions and various other health care products. In order to conform to various labeling laws and other legal requirements relating to such products, it is often necessary for the manufacturer to mark the product containers with the date of manufacture as well as the lot number of the material being sold. In the past, this has normally been done by marking a preprinted label, i.e. a label which has previously been printed with all of the desired information thereon other than the lot number and date, with the lot number and date immediately before or after the bottle is filled. Typically, this is done either by a thermal transfer process or other conventional ink-printing process. Unfortunately, such printing operations are very time consuming and hence represent a real bottleneck in mass producing individually marked flexible bottles rapidly and efficiently.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 -3- In order to overcome this drawback, it has been proposed to employ laser-marking technology to mark the date and lot number on individual bottles. In accordance with one such proposal, the date and lot number are marked directly on the bottle body. Most plastics, however, are transparent to laser light, and accordingly, it is necessary if adopting this proposal to incorporate a material which is opaque to laser light into the plastic forming the bottle body. Such materials are well known and exemplified, for example, in U.S. 4,595,647; U.S. 4,654,290; U.S. 4,753,863; U.S. 4,816,374 and U.S. 4,861,620. See also European Patent 0 190 997 as well as Kilp, Laser Marking of Plastics, Ortech International, Mississauga, Ontario, Canada, copyright ANTEC 1991, pp. 1901-1903. Each of these disclosures is also incorporated herein by reference.
Another material also known to impart laser markability to various types of plastics is titanium dioxide-coated mica particles.
Such materials are sold, for example, under the name AFFLAIR® by E.
Merk Company of Raway, New Jersey and MEARLIN® Lustre Pigments sold by the Mearl Corporation of New York, New York.
Unfortunately, such materials are comparatively expensive.
Accordingly, incorporating such materials into the plastic materials used to form the bodies of the flexible bottles is not cost effective.
In order to deal with this problem, it has also been proposed to laser imprint the labels used on the bottles rather than the bottles themselves. In accordance with one method of applying this technique, a preprinted label is provided with an ink-printed black field and the lot number and date laser imprinted on the black field by burning off the black ink with the laser. Because registration of the laser image with the black field becomes difficult at the high speeds involved in industrial operations, this technique requires a black field of relatively large size to be effective. This, in turn, is regarded by many as being aesthetically unpleasing and is therefore not desired.
Another technique proposed for laser marking flexible plastic labels is to make the labels from a vinyl plastic such as polyvinyl chloride. Carbon dioxide lasers produce high quality, good contrast marks ranging in color from gold to deep orange on polyvinyl chloride films. Unfortunately, many manufacturers also regard this coloration as being aesthetically unacceptable. Also, polyvinyl chloride contains chlorine as well as plasticizers and therefore often produces noxious by-products upon laser bombardment. Accordingly, laser marking of vinyl labels is not attractive.
Accordingly, it is an object of the present invention to provide a method for producing laser-markable labels whose backgrounds are transparent or light in color and which can be easily imprinted with SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 -4easily-readable, high intensity indicia by conventional laser marking technology.
In addition, it is a further object of the present invention to provide a method for producing laser-markable labels as described above which does not adversely affect the various other properties of the label such as ink-printability, die cutability, matrix stripability, dispensability, repositionability and the like.
It is a still further object of the present invention to provide a method for producing ink-printable, laser-markable, flexible, plastic labels which employs a minimum amount of additives and thus is inexpensive to carry out.
It is a still further object of the present invention to provide new flexible, plastic labels for use on flexible plastic bottles which meet all of the foregoing objects as well as to further provide web or sheet stock that can be processed by normal label manufacturing techniques and equipment to provide these labels.
SUMMARY OF THE INVENTION These and other objects are accomplished by the present invention which is based on the discovery that flexible plastic labels which exhibit excellent ink-printability, excellent laser-markability and excellent mechanical properties can be produced by incorporating a suitable laser-opaque material into the core layer of a multilayer coextrudate of the type previously used for labeling flexible plastic bottles.
Surprisingly, it has been found that by burying the laser-opaque materials in the core rather than in the surface layers of these multilayer coextrudates, neither the surface properties of the product, which control its ink-printability, nor the gross mechanical properties of the product, which control the ability of the product to be manipulated properly in modern high speed equipment, are compromised.
At the same time, it has also been found that intense, highly visible contrasting marks can be produced in light-colored or transparent coextrudates made in this manner using conventional laser marking technology even though the laser opaque materials are restricted to the core layer and not present in the product surface where the laser light first impinges on the product.
Accordingly, it is possible in accordance with the present invention to produce flexible, plastic labels for affixing to flexible plastic bottles, as well as webs or sheets of flexible plastic coextrudates useful in manufacturing such labels, which exhibit the same excellent combination of ink-printability and other mechanical properties as prior labels and which at the same time are readily laser-markable with conventional laser marking technology.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 DETAILED DESCRIPTION The present invention utilizes known laser marking technology to impart laser imprinted images to the unique, flexible, plastic labels made in accordance with the present invention.
These unique plastic labels are multilayer coextrudates which are produced by coextrusion of at least two different polymer materials to form a product with at least two and preferably at least three distinct polymer layers bonded together.
In general, such products are composed of an inner core layer and at least one outer skin layer. Usually, the product will have two outer skin layers, one on each side. One of these outer skin layers is typically intended to be ink printable (hereinafter "printing skin"), and accordingly the material used to form this layer and the manner of its extrusion are selected to maximize its ability to accept and retain printing ink. Usually, the other outer skin (hereinafter "bonding skin") is intended for bonding or facilitating bonding of the label to a bottle. Depending on the chemical nature of the core material, the method of bonding and the chemical nature of the bottle, this means that the bonding skin layer can either be adapted to receive a subsequently applied adhesive or, in fact, may constitute the adhesive itself.
For example, where a label having a highly olefinic core layer is intended to be bonded to a bottle with an acrylic latex-based pressure sensitive adhesive, the bonding skin is preferably a material which promotes adhesion of the acrylic adhesive to the olefin core, for example, an olefin copolymer containing polymerized vinyl acetate.
where, however, a label having a highly olefinic core layer is intended to be attached by IMFL to a highly olefinic bottle made, for example, from HDPE (high density polyethylene), the bonding skin layer can itself comprise the heat-activatable adhesive normally used for this purpose. A homopolymer or copolymer of ethylene or propylene is a good example of an appropriate material for this purpose.
The thickness of the inventive labels can vary widely.
Typically, they range between 0.5 and 15 mils, more preferably 1 to mils, even more preferably between about 2 and 5 mils, thick. Of this amount, the printing and bonding skins each occupy about 5 to percent of the thickness of the label, more typically about 10 to percent of the thickness of the label, while the core layer occupies the rest.
In most applications, manufacture of the inventive labels involves production of a continuous sheet or web of the coextrudate, orientation of the web or sheet usually in a single direction (machine direction) only, and finally cutting or otherwise subdividing the web or sheet into individual, discrete labels.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTIUTS95/06258 -6- In the case of pressure sensitive adhesive labels, the coextruded web or sheet after orientation is usually laminated to a release liner comprising the pressure sensitive adhesive, a release agent such as a silicone resin and a paper or film backing layer. The laminate so formed is then typically slit longitudinally into strips and the strips wound up on spools, which are stored and/or sold, as desired.
When it is desired to make and use labels, the laminate strip after unwinding from the spool is fed to a printer/die cutter. This machine ink prints the desired graphics on the coextrudate layer and immediately cuts this layer plus attached adhesive into individual labels. In this cutting operation, a small strip of the coextrudate layer is typically left between adjacent labels so that the coextrudate layer after cutting is composed of a plurality of individual, discrete labels plus an intergral matrix of coextrudate material surrounding the individual labels. This matrix is then removed leaving a strip comprising a continuous paper backing layer carrying discrete, physically separated labels thereon, each label comprising an inkprinted coextrudate with attached pressure sensitive adhesive mounted on the backing layer via a silicone release agent. This strip is then fed to an automatic label applying machine which manipulates the strip, for example, by sliding or rolling the strip around a peel plate at high speed, to cause the individual labels to automatically detach from the backing strip and be projected onto suitably placed bottles.
In the case of IMFL, the procedure is similar, except that the coextruded web or sheet is not laminated to a release layer. Rather, the web or sheet, after optional winding up into bulk rolls for storage, is slit and subjected to printing/die cutting with the individual labels produced thereby being bundled together in a stack.
The blow-molder then loads individual labels from the stack into the label magazine of his blow-molding machine for automatic incorporation into the blow molded bottles as part of the bottle forming operation.
In both IMFL and pressure sensitive adhesive labels, it is conventional to employ coextrudates which have been oriented in the longitudinal, or machine, direction only. Typically, orientation is done by stretching the coextrudate while still hot in the machine direction at a stretch ratio of about 2:1 to about 9:1, with stretch ratios of 4:1 to 6:1 being typical. This results in a significant decrease in overall film thickness as well as adjustment of the mechanical properties of the coextrudate in a known manner. For example, using a 5:1 stretch ratio will reduce the overall extrudate thickness from 16 mils at the extrusion nozzle to approximately 3.2 mils after stretching and will orient the polymer chains in the machine direction to thereby impart considerable stiffness in this direction SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTfUS95/06258 -7but not in the transverse direction. Other known methods for orienting polymer films, for example compression orientation or "blowing" a film produced by extrusion through an annular orifice, can be used.
The hot-stretched coextrudates produced as described above can also be annealed or "heat set" in accordance with known techniques.
Typically, this is done after extrusion and initial chilling of the extrudate by reheating the extrudate to an elevated temperature, for example, 300 0
F.
After coextrusion, orientation, heat setting, etc., the coextrudates can be directly processed into labels. More typically, however, the coextrudates are taken up wound around) suitable cores to form rolls of material typically containing 500 to 15,000, preferably 2,000 to 10,000, linear meters of material in the form of continuous sheets or webs. Such rolls, which can be subdivided radially cut in planes perpendicular to their axes to form rolls of smaller axial width) or left as is, can be stored, shipped and sold for use as needed.
Processes for forming coextrudates in the manner described above for use as flexible labels for flexible bottles are well known in the art and shown, for example, in the above-identified patents. Any such procedure can be used in accordance with the present invention.
The coextrudates of the present invention can be formed from any materials commonly employed for making coextrudate flexible plastic labels. For example, a suitable material for making the core layer for many applications in accordance with the present invention is polyethylene of low, medium or high density between 0.915 and 0.965 specific gravity. This is a relatively low cost, extrudable filmforming material whose stiffness is dependent, among other things, on the density selected and whose body and strength are sufficient for most uses. Polyethylene of lower densities, down to a specific gravity of 0.890, may be employed for greater flexibility.
A preferred material for the core layer is polypropylene (or a propylene copolymer) having a flex modulus ranging between about 130,000 and 300,000 psi at 73 0 depending on the stiffness desired.
Still other preferred materials for forming the core layer comprise copolymers of olefin monomers with ethylenically unsaturated carboxylic acid ester comonomers, such as ethylene-vinyl acetate copolymer, as well as blends of such copolymers with any and all of the other polymers and copolymers described above. Still other preferred materials comprise physical blends of polypropylene or copolymers of polypropylene and polyethylene and ethylene-vinyl acetate (EVA) in weight ratios ranging from 50/50 to 80/20, preferably 55/45 to 65/35.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTIUS95/06258 -8- For clear label applications, a physical blend of a copolymer of polypropylene and polyethylene and ethylene-vinyl acetate (EVA) is also preferred. For opaque film labels applications, a preferred core layer is a physical blend of polypropylene and EVA.
Polystyrene is also a candidate material for the core layer particularly where a stiffer label is desired.
In order to make core layers opaque, various inorganic fillers may be incorporated into the polymer forming the layer. Useful fillers include calcium carbonate, titanium dioxide and blends thereof.
Pigments and dyes can also be added for imparting color thereto.
Examples of materials found suitable for the skin layers of the inventive labels are materials which are formed predominantly from polyolefins. By being formed "predominantly from polyolefin" is meant that the layer is formed from a homopolymer or copolymer of a polyolefin or blends of such homopolymers and/or copolymers, with the proviso that at least 50% of the polymerized monomers in the layer are polyolefins. Examples of such materials are homopolymers and copolymers of ethylene and propylene such as polyethylene, polypropylene and ethylene/propylene copolymer, copolymers of olefin monomers with ethylenically unsaturated carboxylic acid or ethylenically unsaturated carboxylic acid ester comonomers such as ethylenevinyl acetate copolymer (EVA) and blends of such homopolymers and copolymers. In many applications, the polymers, copolymers and blends described above in connection with the core layer can be used.
Other materials useful for making the outer skin layers of the inventive labels include meltable film-forming substances used alone or in combination such as polyethylene methyl acrylic acid, polyethylene ethyl acrylate, polyethylene methyl acrylate, acrylonitrile butadiene styrene polymer, polyethylene vinyl alcohol, nylon, polybutylene, polystyrene, polyurethane, polysulfone, polyvinylidene chloride, polypropylene, polycarbonate, polymethyl pentene, styrene maleic anhydride polymer, styrene acrylonitrile polymer, ionomers based on sodium, potassium, calcium or zinc salts of ethylene/ methacrylic acid, polymethyl methacrylates, cellulosics, fluoroplastics, polyacrylonitriles, and thermoplastic polyesters.
The preferred materials to use in forming both the core and the skin layers of the inventive coextrudates are basically matters of choice and depend on the particular applications involved. The foregoing patents and publications incorporated herein by reference go into great detail in explaining how to pick particular materials for particular uses and these techniques can also be used in accordance with the present invention to design a particular coextrudate for a particular utility.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 -9- In accordance with the present invention, flexible plastic labels as described above are made laser-markable by including in the core layer of the label a laser-opaque material. By laser-opaque material is meant any material which will absorb or reflect laser light so as to cause marking of the polymer layer in which the laser-opaque material is contained. Surprisingly, it has been found that the intensity of the marks made as a result of laser marking will not be compromised, and in fact may be improved, by restricting the laseropaque materials to the core of the extrudate rather than in its skins.
Moreover, keeping the laser-opaque material out of the skins also has the beneficial effect of not deleteriously affecting the physical properties, particularly the smoothness of the skins or their chemical nature either. Furthermore, by keeping the laser-opaque material in the core only, the coextrudates can be made without adversely affecting the various mechanical properties such as dimensional stability, stiffness, high speed dispensability, die cutability, matrix stripability, repositionability and the like of the label product.
Any type of laser-opaque material can be employed in accordance with the present invention. In this connection, there are many materials known for their ability to absorb and/or reflect laser light of different wave lengths and energy densities and, as a result, "interact" with a polymer material in which they are contained to cause a visible mark to form. The type of "interaction," thermal degradation of the polymer, simple chemical reaction, generation of gas bubbles, etc., varies depending on the type and operation of the laser employed as well as the type of polymer material employed, and accordingly there must be a "match" of the laser-opaque material with the polymer employed as well as the type and operation of the laser employed. In accordance with the present invention, any known laseropaque material can be employed, so long as it "matches" both the polymer as well as the type and operation of the laser employed.
The preferred laser-opaque materials used in accordance with the present invention are solid, particulate materials. Solid particulate materials having a high aspect ratio, particularly those which have a platelet structure, are especially preferred. When particulate materials are used, it is preferable that they have an average particle size from 0.2 to 400, preferably 0.5 to 60, most preferably 1 to microns.
Examples of this type of laser-opaque materials for use in the present invention, particularly with respect to CO, TEA lasers as discussed below, are kaolin, mica, mixtures of mica and titanium dioxide and wollastonite. Also useful are the various types of laser markable materials shown in the following patents, the disclosures of which are incorporated herein by reference: European Patent 0 190 997; SUBSTITUTE SHEET (RULE 26) WO 95134263 PCT/US95/06258 U.S. 4,595,647; U.S. 4,654,290; U.S. 4,753,863; U.S. 4,816,374 and U.S.
4,861,620.
Especially preferred laser-opaque materials are titanium dioxide-coated mica particles. These materials are commercially available from E. Merck Corporation of Hawthorne, New York under the designation AFFLAIR® and The Mearl Corporation of New York, New York under the designation of MEARLIN® luster pigments. These materials typically have particle sizes of 1 to 200, preferably 1 to 60, more preferably 1 to 25 microns.
The amount of laser-opaque material to be incorporated into the core layer of the inventive coextrudate products can vary widely.
Basically, the minimum amount is that amount which is sufficient to form a visible marking of the desired intensity. The maximum amount, in turn, is usually dictated by economics, amounts over that necessary to produce a mark of a desired intensity being unnecessary. Typically, the amount will be on the order of 0.1 to 10 percent by weight, based on the weight of the material forming the core layer (including any other filler or pigment such as titanium dioxide, calcium carbonate and the like). More typically, the amount of laser-opaque material will be on the order of about 0.5 to 5 percent by weight.
In this regard, it is convenient to refer to the amount of laser opaque material in the core layer of the inventive labels in terms of effective thickness. By "effective thickness" is meant the number obtained by multiplying the thickness of the core layer, measured in mils, times the concentration of the laser-opaque material in the core layer, measured in weight percent expressed as a decimal. Measured in this way, it is preferable that the amount of laser opaque material in the core layer be enough so that the effective thickness thereof is 0.005 to 0.15, more preferably 0.01 to 0.10, even more preferably 0.02 to 0.06.
In order to laser imprint the desired image or information onto labels made in accordance with the present invention, the labels are irradiated with laser light containing or embodying the desired information or image therein.
As a practical matter, only three basic types of marking lasers are now available commercially. These are eximer lasers based on rare earth gas halides, Nd/YAG systems and pulsed carbon dioxide lasers. Of these, the Nd/YAG systems and carbon dioxide lasers are typically used for plastics. However, eximer lasers have also been used for this purpose. In accordance with the invention, each of these types of lasers can be used, although pulsed carbon dioxide TEA (transverse excited atmosphere) lasers are preferred from the point of view of cost and reliability.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 -11- The conditions of laser marking vary widely and are dependent on a number of factors such as the identity and amounts of laser-opaque materials in the films, film thickness and the like.
In the case of the preferred TEA carbon dioxide laser (wave length 10.6 micrometers infrared range), energy densities on the order of 0.8 to 36, preferably 1.8 to 28.8, Joules per square centimeter per pulse at pulse durations of 50 to 1,000, preferably 100 to 300, nanoseconds are appropriate.
The particular operating variables of the laser to employ in a particular embodiment of the invention can be easily determined by routine experimentation. As well appreciated by those skilled in the art, the rate in which energy is supplied by the laser should not be so great that the film is destroyed or otherwise unacceptably degraded but yet needs to be enough so that indicia of suitable intensity will be produced.
In order to imprint a label by the laser marking technique of the present invention, the laser beam generated by the laser is passed through a suitable stencil containing the desired information to generate an information-containing laser beam. This beam is then focused onto the label to be marked and the label irradiated with the laser light for the imprinting process. Exactly how this is done is well known to those skilled in the art of laser marking, and any conventional procedure for this purpose can be employed in accordance with thepresent invention.
WORKING EXAMPLES In order to more thoroughly illustrate the present invention, the following working examples are presented.
In these examples, a hot coextrudate was produced in accordance with the process described in U.S. 5,242,650 with a total thickness of 17.5 mils. The coextrudate was then hot stretched to make a film of mils. In each example, the coextrudate was made with two identical skins, each skin layer making up 10% of the total thickness of the coextrudate and the remainder comprising the core.
After manufacture, each film was them imprinted with a simulated date and lot code by means of a Blazer 6000 Pulsed Carbon Dioxide Laser made by Lasertechnics Corporation of Albuquerque, New Mexico. The laser beam produced was passed through a mask having a simulated date and lot code about one inch wide and then focused to a reduced size onto the target film to imprint the image thereon. Imprinting was done at different energy levels (3 and 4 Joules per pulse) and different reduction ratios (ratio of mask size to image size) In these experiments, the laser beam as produced by the laser has an energy density of 0.8 Joules/cm 2 at a maximum energy of SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95106258 -12- Joules. The energy density of the beam as it strikes the target can be reduced from this value by reducing the energy of the laser or increased by reducing (narrowing) the beam size between the mask and the surface of the target. In the following working examples, the approximate energy densities of the laser beam striking the targets were as follows: Pulse Energy 4 Joules 4 Joules 3 Joules 3 Joules Reduction Ratio 2.75:1 2.0:1 2.75:1 2.0:1 Energy Density 5 Joules/cm 2 3 Joules/cm 2 4 Joules/cm 2 2 Joules/cm 2 Two masks were used to optimize the width of the image to give four 0.95" character for the 2:1 size reduction (reduction ratio), and two rows of 0.90" characters for the 2.75:1 size reduction. The larger characters apparently influenced the visual impact of the mark, as the mark contrast seems to be higher for the larger mark than the energy density would predict, as more fully illustrated below." The laser produces silvery-gray laser imprinted marks. The images so produced were visually observed and rated using an arbitrary scale of from 0 (no mark) to 10 (black and very distinct).
The following examples were conducted: Example 1 A coextrudate having the following composition was produced: Table 1 Printing Skin Core Layer Bonding Skin Polypropylene homopolymer (HPP) Ethylene-vinyl acetate copolymer (EVA-18% VA) Calcium particulate carbonate concentrate particulate CaCO 3 in HPP) Ethylene-vinyl acetate copolymer (EVA-18% VA) Titanium dioxide concentrate Rutile TiO, in HPP) AFFLAIR 110 concentrate TiO 2 coated mica in HPP) Polypropylene homopolymer (HPP) Ethylene-vinyl acetate copolymer (EVA-18% VA) Weight The results are obtained by laser-imprinting their coextrudate in the manner described above.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTIUS95/06258 -13- Table 2 Concentration of AFFLAIR 110 Example in core
AFFLAIR
Effective Thickness Visual Intensity of Image at different energy intensities and Reduction Ratios 3 Joules RR RR 4 Joules RR RR 2:1 2.75:1 2:1 2.75:1 0.056* 7 7 7 (3.5 mils) x x x 0.056 Table 2 shows that the laser marking technique as described above produced images having a fairly high degree of contrast or intensity under essentially all the conditions tried in the experiment. This shows that images of good intensity can be produced in accordance with the present invention, even though the laser-opaque material is buried in the core and not present in the skin layers.
Examples 2-6 Example 1 was repeated except that initial film thickness was mils before stretching and final fill thickness was 3 mils after stretching. In addition, the amount of laser-opaque material in the core was varied from 0 to 3.8 weight percent, based on the weight of the core, to illustrate the effect of varying concentration of this material. The specific compositions of the different layers used in these examples is set forth in the following Table 3. Unless otherwise indicated, the polymers and copolymers used have the same compositions as in Example 1: Table 3 Printing Skin Core Layer Bonding Skin Polypropylene homopolymer Ethylene-vinyl acetate copolymer (EVA) Polypropylene-maleic anhydride graft copolymer (0.25 weight maleic anhydride) Propylene-ethylene random copolymer (3.2 weight ethylene) Ethylene-vinyl acetate copolymer (EVA) Titanium dioxide concentrate TiO 2 /50% polypropylene) Polypropylene-maleic anhydride graft copolymer AFFLAIR 110 concentrate (40% in EVA) Polypropylene homopolymer Ethylene-vinyl acetate copolymer Polypropylene-maleic anhydride graft polymer
X
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 -14- The following results were obtained: Table 4
AFFLAIR
Concentration i.e., Amount of EVA Example AFFLAIR 110' Concentration of AFFLAIR 110 in core (wt t) X AFFLAIR Effective Thickness Visual Intensity of Image at different energy densities and Reduction Ratios 3 Joules RR RR 2:1 2.75:1 4 Joules RR RR 2:1 2.75:1 0 0 3 3 4 4 5 6+ 7 0.6 .0144 2 2.4 0.96 .023 3 4.75 1.9 .0456 4+ 3.8 .0912 5+ *Equals X/0.4 since AFFLAIR is 40% of the AFFLAIR 110/EVA concentrate 2 3 5 The foregoing results show that the contrast of the visual images produced in accordance with the present invention increases proportionally with the effective thickness of the laser-opaque material in the core layer. In addition, these examples show that the images produced appear to be more intense at higher reduction ratios and also at higher laser impulse energy levels.
Examples 7-9 Example 1 was repeated except that the coextrudates in Examples 7 and 8 had the composition set forth in the following Tables 5 and 6: Table Printing Skin Core Layer Bonding Skin Polypropylene homopolymer (HPP) Ethylene-vinyl acetate copolymer (EVA) Polypropylene-maleic anhydride graft copolymer Propylene-ethylene copolymer Ethylene-vinyl acetate copolymer (EVA) Titanium dioxide concentrate Polypropylene-maleic anhydride graft copolymer AFFLAIR 110 concentrate (20% in EVA) Polypropylene homopolymer Ethylene-vinyl acetate copolymer Polypropylene-maleic anhydride graft polymer Table 6 Printing Skin Core Layer AFFLAIR 110 concentrate (20% in HPP) Ethylene-vinyl acetate copolymer (EVA) Polypropylene-maleic anhydride graft copolymer Propylene-ethylene copolymer Ethylene-vinyl acetate copolymer (EVA) Titanium dioxide concentrate Polypropylene-maleic anhydride graft copolymer SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 Printing AFFLAIR 110 concentrate (20% in HPP) Skin Ethylene-vinyl acetate copolymer (EVA) Polypropylene-maleic anhydride graft copolymer Bonding AFFLAIR 110 concentrate (20% in HPP) Skin Ethylene-vinyl acetate copolymer Polypropylene-maleic anhydride graft polymer In addition, in Example 9, a single layer extrudate was used, this single layer having the same composition as the core layer of Example 7 and the same overall thickness as the total extrudate thickness of Example 7.
The following results were obtained: Table 7 Relative Thickness of Concentration Layer of AFFLAIR Containing 110 in Visual Intensity of Image at Afflair Active Layer AFFLAIR Effective Differing Energy Intensities and Example (3 mils total) (wt Thickness Reduction Ratios 3 Joules 4 Joules RR RR RR RR 2:1 2.75:1 2:1 2.75:1 7 80% 1.0 .024 3 3 4 4+ 8 10% 8.0 .024 <1 Holes <1 Holes 9 100% 1.0 .030 3 3 4 4+ Examples 7 and 8 compare the effect of placing the laser-opaque material in the core rather than in the skin. In this regard, note that the calculations of effective thickness in Example 8 assume that only the outer skin layer is effected by the laser impregnation. In other words, in assessing the visual impact of a laser impregnation, any effect on the lower skin layer is disregarded.
Example 7, illustrating the present invention, shows that when the laser-opaque material is present in the core layer at an effective thickness of 0.024, visual images having significant contrast are produced at all operating conditions. On the other hand, when the same amount of laser-opaque material as used in the core of Example 7 is placed in the printing skin of the Example 8 composite, images with little if any contrast are produced at reduction ratios of 2:1, while holes are produced in the printing skin at the higher reduction ratio of 2.75:1. This shows that the images produced by laser marking are not simply a result of the amount of laser opaque material in the system but also depend on where it is located. In addition, this also shows that locating the laser opaque material in the core, rather than in the skin layer which first receives the laser light impinging on the article provides a significantly, and unexpectedly, superior result.
To show the effect of not having any skins at all, Example 9 was conducted. In this example, a single layer extrudate having the same SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTfS95/06258 -16thickness as the coextrudates of Examples 7 and 8 was filled with the same concentration of laser opaque material as in the core of the Example 7 coextrudate. This means that the Example 9 extrudate contained a significantly greater overall amount of laser-opaque material than the coextrudate of Example 7. Notwithstanding this greater amount of active ingredient, the images produced in the Example 9 coextrudate have essentially the same visual impact as those of the Example 7 coextrudate.
This shows that burying the laser-opaque material in the core and thereby keeping the laser-opaque material out of the skins does not adversely impact the contrast or intensity of the images produced.
This, in turn, shows that images of acceptable contrast can be produced with less overall laser-opaque material and further that this advantageous result can be obtained while the outer and inner skin layers are maintained free of this material so that they can retain their smoothness and ink-printability properties. This also means that it is possible to adopt the use of laser marking with opaque materials in such a way that the laser opaque material is kept away from the mechanical equipment involved in processing, such as the die lips of the extrusion die, or the calender rolls used in subsequent processing.
This prevents die lines from appearing in the product as well as excessive wear on the die lips and other equipment which would otherwise occur.
Incidentally, note that the results obtained in Example 7 are almost identical to those obtained in Example 4 in which the coextrudate had an effective thickness of laser-opaque material of 0.023. This, in turn, shows that "effective thickness" is a meaningful number.
Examples 10-14 Examples 2 to 6 were repeated except that the Afflair additive was Afflair 100, rather than Afflair 110. Afflair 100 is slightly larger in particle size, and as can be seen below appears to be slightly less effective.
Also, in some of Examples 10-14, a single layer extrudate was produced rather than a multi-layer extrudate, while in one of these examples, Example 14, the extrudate was not oriented after extrusion but was simply produced as cast.
SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCT/US95/06258 -17- The results obtained are set forth in the following Table 8: Table 8 Concentration of
AFFLAIR
Total 100 in MDO' Visual Intensity of Image Multi thickness Active or Effect. at Different Energy Intensi- Example Layer? mils Layer Cast Thick. ties and Reduction Ratios 3 Joules 4 Joules RR RR RR RR 2:1 2.75:1 2:1 2.75:1 No 2.8 0.9 MDO .0252 2+ 3 3 Holes 11 Yes 3.5 0.9 MDO .0252 2+ 3 3 4 12 No 3.0 0.9 MDO .027 2+ 3 3 4 13 Yes 3.5 2.1 MDO .0588 4 4 4+ 14 No 3.0 2.1 Cast .0588 4 4 4 4 Oriented in the machine direction only Comparison of Examples 10 and 11 in the above Table 8 shows that providing an extrudate with protective skins as accomplished in accordance with the present invention, does not hurt and also may even prevent burn through at more intense conditions. Note in particular that the composite of Example 11 is essentially the same as Example in terms of the active thickness and active ingredient concentration, the only difference between that in Example 11, protective skins having no laser-opaque material therein are provided. This is significant in that it shows the coextrudated skins can be fine tuned to meet performance criteria without reducing laser-markability at the same additive cost.
Comparison of Example 12, in which a single layer extrudate thicker than that of Example 10 and hence having more overall laseropaque material than in Examples 10 or 11 (0.027 effective thickness rather than 0.0252) shows that the visual impact of this extrudate is no better than that of the coextrudate of Example 11 even though the extrudate of Example 12 has more laser-opaque material.
Examples 13 and 14 are comparable in that both have the same effective thickness of laser-opaque material. However, the Example 14 product, which is a single layer extrudate not subjected to orientation, provides a visual impact which is noticeably less intense than that provided by the Example 13 product which is composed of multiple layers having been oriented in the machine direction. This shows that the combination of burying the laser-opaque material in the core and orienting in at least the machine direction facilitates reduction in the amount of expensive laser-opaque material necessary to produce a visually acceptable image.
SUBSTITUTE SHEET (RULE 26) WO 95134263 PCTIUS95/06258 -18- Example The procedure of Examples 2 to 7 was repeated except that the thickness of the coextrudate passing out of the extrusion die was 12.5 mils and the coextrudate so made was stretched to a final product thickness of 2.5 mils. Also, the composition of the individual layers of the coextrudate was changed so that the coextrudate product was a slightly hazy, essentially transparent film. The compositions of the individual layers of the coextrudate are set forth in the following Table 9: Table 9 Printing Polypropylene homopolymer Skin Ethylene-vinyl acetate copolymer (EVA) Polypropylene-maleic anhydride graft copolymer Core Layer Propylene-ethylene copolymer Ethylene-vinyl acetate copolymer (EVA) 32.5 Polypropylene-maleic anhydride graft copolymer AFFLAIR 110 concentrate (40% in EVA) Bonding Polypropylene homopolymer Skin Ethylene-vinyl acetate copolymer (EVA) Polypropylene-maleic anhydride graft copolymer The results obtained are set forth in the following Table Table Concentration of AFFLAIR 110 in Active AFFLAIR 110 Visual Intensity of Images in Layer Effective at Different Energy Intensities and Example (wt Thickness Reduction Ratios 3 Joules 4 Joules RR RR RR RR 2:1 2.75:1 2:1 2.75:1 1.0 0.020 8 8 8 8 From Table 10, it can be seen that under all operating conditions, a very high visual impact image was produced even though the effective thickness of the laser-opaque material in the active layer was relatively low. This illustrates that the present invention is particularly .effective in providing laser-markable images on transparent labels.
Example 16 The following example demonstrates the present invention is readily applicable to making in-mold, machine direction oriented labels.
The recipe for an opaque white flexible film with a print layer, and an adhesive layer, is as follows: SUBSTITUTE SHEET (RULE 26) WO 95/34263 PCTUS95/06258 -19- Table 11 Top Polypropylene homopolymer Ethylene-vinyl acetate copolymer (EVA) Central Propylene-ethylene copolymer Ethylene-vinyl acetate copolymer (EVA) Titanium dioxide concentrate AFFLAIR 110 concentrate (16% in EVA) Bottom Low-density polyethylene (LDPE) 24 Ethylene-vinyl acetate copolymer (EVA) Anti-block concentrate (20% in polyethylene) 36 The above film was coextruded as in previous Examples 2 through 7, but the coextrudate thickness was 20 mils, and stretching was done to produce a film of 4.0 mils. As in the previous examples, the thickness of the top and bottom layers were each 10% of the total, the central layer making up the remaining Table 12 Concentration of AFFLAIR 110 in Active Visual Intensity of Images at in Layer Effective Different Energy Intensities and Example (wt Thickness Reduction Ratios 3 Joules 4 Joules RR RR RR RR 2:1 2.75:1 2:1 2.75:1 16 0.8 0.020 2+ 2+ 4 4 Although only a few embodiments of the present invention have been described above, it should be appreciated that many modifications can be made without departing from the spirit and scope of the present invention. For example, although the multi-layer coextrudates of the present invention have been described above in terms of three layers, it should be appreciated that any number of plural layers can be employed. For example, where necessary, suitable tie layers for bonding dissimilar skin and core layers can be employed. In addition, a bonding skin layer may be unnecessary in some instances, particularly wherein a heat sensitive adhesive exhibiting good adhesion to the core layer is or will be employed. All such modifications are intended to be included in within the scope of the present invention, which is to be limited only by the following claims.
SUBSTITUTE SHEET (RULE 26) m Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification, they are to be interpreted as specifying the presence of the stated features, integers, steps or components referred to, but not to preclude the presence or addition of one or more other feature, integer, step, component or group thereof.
8/1/99TD8991
Claims (3)
1999-07-02 15:56 CALLINAN LAWRIE -21 The claims defining the Invention are as follows; 1. A process for forming a visual image on an ink-printable, flexible, plastic label, said label including a coextrudate of a core layer and at least one skin layer, said core layer containing a laser-opaque material therein, said skin layer being free of laser opaque material and further being capable of receiving and retaining an Ink-printed Image thereon, said process including irradlatihg said coextrudate with laser light in the form of said printed image to cause said ink-printed visual Image to form In said core layer.
2. The process of Claim 1, wherein said at least one skin layer has an ink-printed image thereon. 5
3. The process of Claim 1 or Claim 2, wherein the thickness of said 90:0 core layer is at least 50% of the thickness of said coextrudate. The process of any one of Claims 1 to 3, wherein the thickness of said at least one skin layer is from 5 to 15% of the thickness of said S S coextrudate. 5. The process of any one of Claims 1 to 5, wherein said core 16yer and said at least one skin layer are formed predominantly from polyolefin. 6. The process of any one of Claims 1 to 5, wherein said laser- opaque material is titanium dioxide-coated mica. 7. The process of Claim 6, wherein the particle size of said laser- opaque material is from 0.5 to 200 microns. 8. The process of any one of the preceding Claims, wherein the effective thickness (as hereinbefore defined) of said laser-opaque material In said core layer is from 0.005 to 0.15. 9. The process of any one of the preceding Claims, wherein said core layer and said at least one skin layer contain copolymerized vinyl acetate. The process of any one of the preceding Claims, wherein said coextrudate contains a skin layer on each side of said core layer. 11. An ink-printable, flexible, plastic label capable of generating a Visual image therein when irradiated with laser light, said label including a coextrudate I' I 1 02/07 99 FRI 15:48 [T/RX NO 8637 00 02/07 '99 FRI 15:48 [TX/RX NO 8637] E008 61 3 98194600 P.09 1999-07-02 15:57 CRLLINRN LAWRIE 6 8960 P0 22- of a core layer and at least one skin layer, said core layer containing a laser- opaque material responsive to said laser light in an amount sufficient to c~use a visual image to form in the areas of said core layer which are irradiated With said laser light, said at least one skin layer being capable of receiving and retaining an Ink-printed image thereon, said at feast one skin layer also being free of said laser-opaque material. 1 2. The label of Claim 11, wherein said core layer and said at least one skin layer are formed predominantly from polyolef in. 1 3. The label of Claim 11 or Claim 12, wherein the effective thickness 000eq: (as hereinbefore defined) of said laser-opaque material In said core layer I$ from 5 0.005 to 0. 14. The label of any one of Claims 11 to 13, wherein the particle size of said laser-opaque material is from 0.5 to 400 microns. The label of any one of Claims 11 to 15, wherein said laser-qpaque material is titanium dioxide-coated mica. 16. The label of any one of Claims 11 to 15, wherein said core layer and said at least one skin layer contain copolymerized vinyl acetate, 17. The label of any one of Claims 11 to 16, wherein said coextrudate Is oriented In a single direction only. 18. The label of any one of Claims 11 to 17, wherein said label 25 Includes a first skin layer on one side of said core layer and a second skin layer on the other side of said core layer, said first skin layer being free of said laser- :opaque material. 1 9. The label of Claim 18, wherein said second skin layer Is also -free of said laser-opaque material. 20, The label of Claim 18 or Claim 1 9, wherein said second layer includes a heat activated adhesive. 21. The label of Claim 1 9, further including a pressure sensitive adhesive attached to said second skin layer. 22. A combination Including a flexible plastic bottle and the label of V7 002/07 '99 FRI 15:48 [TX/RX NO 8637] ZI009 1999-07-02 15:57 CRLLINAN LAWRIE 61 3 98194600 23 claim 11 Integrally attached to said bottle. 23. The combination of Claim 22, wherein said label is attached to said bottle by means of a pressure sensitive adhesive. 24. The combination of Claim 22, wherein said label Is attached to said bottle by means of a heat activatable adhesive. 25. A process for affixing a label to a flexible plastic bottle, said label being integrally affixed to said bottle and capable of flexing with said bottle without detachment therefrom, said label bearing an ink-printed Image as well as a laser-generated image, said process including affixing the label of Claim 11 to said bottle after said ink-printed image is applied to said label and thereafter marking said laser-generated image on said label by Irradiating said label with laser light embodying said laser-generated image. 26. A bottle having a label affixed thereto by the process of Claim 27. A coextrudate useful for the manufacture of labels by subdividing said coextrudate into a plurality of said labels, said coextrudate including a flexible web or sheet of plastic material, said web or sheet being formed from a core layer and at least one skin layer, said core layer containing a laser-opaque material responsive to laser light in an amount sufficient to cause a visual image to form in the areas of said core layer which are irradiated with said laser light, said at least one skin layer being capable of receiving and retaining an Ink- printed image thereon, said at least one skin layer also being free of said laser- opaque material. 28. A roll of material including the coextrudate of Claim 27 In the form a. of a continuous web or sheet having a length of at least 500 meters, said web or sheet being wound around itself to form said roll. 29. The process of any one of Claims 1 to 10, wherein the identity and amount of said laser-opaque material In said core Is sufficient so that said visual image forms when said label is irradiated with a pulsed laser, The process of Claim 29, wherein said pulsed laser produces laser light with a pulse duration of from 50 to 1,000 nanoseconds. i li U r 02/07 '99 FRI 15:48 [TX/RX NO 8637] R010 1999-07-02 15:58 CALLINFN LAWRIE 61 3 98194600 P.11 24- 31. The process of Claim 30, wherein said laser is a C0 2 laser producing laser light with a wave length of 10.6 micrometers. 32. The process of Claim 31, wherein the energy density of said laser light is from 0.8 to 36 Joules per square centimeter per pulse. 33. The process of Claim 32, wherein the amount of said laser-opaque material in said core layer is from 0,1 to 10 weight percent based on the weight of said core layer. 34. The process of any one of Claims 8 to 10 and 29 to 33, wherein said effective thickness of said laser opaque material In said core layer (as Shereinbefore defined) from 0.01 to 0.10. 15 35. The process of Claim 34, wherein said effective thickness is from S 0.02 to 0.06. 36. The label of any one of Claims 11 to 21, wherein the identity and amount of said laser-opaque material in said core is sufficient so that said visual image forms when said label Is Irradiated with a pulsed laser. 37. The label of Claim 36, wherein said pulsed laser produces laser light with a pulse duration of from 50 to 1,000 nancseconds. 38. The label of Claim 36, wherein said laser is a CO 2 laser producing laser light with a wave length of 10.6 micrometers. 39. The label of Claim 38, wherein the energy density of said laser length is from 0.8 to 36 Joules per square centimeter per pulse. The label of any one of Claims 11 to 21 and 36 to 39, wherein the amount of said laser-opaque material in said core layer is 0.1 to 10 weight percent based on the weight of said core layer. 41. The label of any one of Claims 11 to 21 and 36 to 40, wherein said effective thickness (as hereinbefore defined) of said laser-opaque material in said core layers from 0.01 to 0.10, 42. The label of Claim 41, wherein said effective thickness (as hereinbefore defined) is from 0.02 to 0.06. 43. A process for forming a visual image on an ink-printable, fledxble, /21r 1 9I.,P.z1 02/07 '99 FRI 15:48 [TX/RX NO 8637] IM011 P. 12 1 1999-07-02 15:59 CRLLINRN LRWRIE 6 8960 P1 61 3 98194600 25 plastic label, substantially as described herein with reference to any one of the Examples. 44. An ink-printable, flexible, plastic label, as claimed In Claim 11, substantially as described herein with reference to any one of the Examplbe. Dated this 2 11d day of July, 1999 S 9e*S 99 0 *990 0e 9* 9 *9 09 9 *900 S. 9 SS .9 AVERY DENNISON By their Patent Attorneys: CALLINAN LAWRIE foe. 0 of9 ,7~rn~%91.Eg.25 02/07 '99 FRI 15:48 [TX/RX NO 86371 R j012
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US25930194A | 1994-06-13 | 1994-06-13 | |
US08/259301 | 1994-06-13 | ||
PCT/US1995/006258 WO1995034263A1 (en) | 1994-06-13 | 1995-06-06 | Laser-markable plastic labels |
Publications (2)
Publication Number | Publication Date |
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AU2690195A AU2690195A (en) | 1996-01-05 |
AU709752B2 true AU709752B2 (en) | 1999-09-09 |
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AU26901/95A Ceased AU709752B2 (en) | 1994-06-13 | 1995-06-06 | Laser-markable plastic labels |
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EP (1) | EP0766546B1 (en) |
AT (1) | ATE201318T1 (en) |
AU (1) | AU709752B2 (en) |
BR (1) | BR9508699A (en) |
CA (1) | CA2192850A1 (en) |
DE (1) | DE69521045T2 (en) |
ES (1) | ES2157329T3 (en) |
WO (1) | WO1995034263A1 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19509505C1 (en) * | 1995-03-16 | 1996-01-25 | Beiersdorf Ag | Multilayer laser codable label |
FR2762425B1 (en) * | 1997-04-18 | 1999-06-04 | Chevillot Sa | INFALSIFIABLE, INDELEBILE AND CONTRAST MARKING OF OBJECTS AND PARTICULARLY LABELS |
US6054006A (en) * | 1997-12-01 | 2000-04-25 | Great Pacific Enterprises, Inc., Through Its Division, Montebello Packaging | Method and apparatus for applying a printed label to a metal container and the labeled container produced thereby |
DE19913323B4 (en) * | 1999-03-24 | 2004-03-25 | Cleanpack Gmbh Innovative Verpackungen | Method of making labels |
US6180318B1 (en) | 1999-05-19 | 2001-01-30 | 3M Innovative Properties Company | Method of imaging an article |
US8048605B2 (en) | 2001-03-16 | 2011-11-01 | Datalase Ltd | Laser-markable compositions |
JP3913680B2 (en) | 2001-03-16 | 2007-05-09 | データレイズ・リミテッド | Composition for laser marking |
FR2833518B1 (en) | 2001-12-14 | 2004-06-25 | Gemplus Card Int | LASER MARKED INFORMATION MEDIUM |
US9387652B2 (en) * | 2005-01-10 | 2016-07-12 | Avery Dennison Corporation | Removable curl labels |
WO2008057926A2 (en) | 2006-11-02 | 2008-05-15 | Avery Dennison Corporation | Emulsion adhesive for washable film |
AT507507A1 (en) * | 2008-11-03 | 2010-05-15 | Teich Ag | CIRCUIT BOARD |
JP5379859B2 (en) | 2008-11-05 | 2013-12-25 | エグザテック・リミテッド・ライアビリティー・カンパニー | Partial marking of coated plastic substrate |
DE202009002784U1 (en) | 2009-02-27 | 2009-05-20 | Dittrich, Alwin | Labeled sheet material and labeling device |
CA2757447C (en) | 2009-03-30 | 2017-10-24 | Avery Dennison Corporation | Removable adhesive label containing high tensile modulus polymeric film layer |
CN102449677B (en) | 2009-03-30 | 2016-02-03 | 艾利丹尼森公司 | Containing the removable adhesive label with hydrophilic macromolecule membranous layer |
US20120018098A1 (en) | 2009-03-30 | 2012-01-26 | Avery Dennison Corporation | Removable Adhesive Label Containing Inherently Shrinkable Polymeric Film |
BR112012004532A2 (en) * | 2009-08-31 | 2017-05-30 | 3M Innovative Proferties Company | "laser engraving process articles" |
US10687588B2 (en) | 2014-10-22 | 2020-06-23 | 3M Innovative Properties Company | Printed components and methods for making the same |
CA3071576C (en) * | 2017-08-11 | 2023-07-04 | Husky Injection Molding Systems Ltd. | Molded article, container and a method for printing thereon |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4816374A (en) * | 1985-04-12 | 1989-03-28 | Societe D'applications Plastiques Rhone-Alpes (Sapra) | Method of making a plastic material sensitive to laser radiation and enabling it to be marked by a laser, and articles obtained thereby |
Family Cites Families (1)
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US5143570A (en) * | 1985-02-05 | 1992-09-01 | Avery Dennison Corporation | Composite facestocks and liners |
-
1995
- 1995-06-06 BR BR9508699A patent/BR9508699A/en not_active IP Right Cessation
- 1995-06-06 AU AU26901/95A patent/AU709752B2/en not_active Ceased
- 1995-06-06 EP EP95922091A patent/EP0766546B1/en not_active Expired - Lifetime
- 1995-06-06 AT AT95922091T patent/ATE201318T1/en not_active IP Right Cessation
- 1995-06-06 WO PCT/US1995/006258 patent/WO1995034263A1/en active IP Right Grant
- 1995-06-06 ES ES95922091T patent/ES2157329T3/en not_active Expired - Lifetime
- 1995-06-06 DE DE69521045T patent/DE69521045T2/en not_active Expired - Fee Related
- 1995-06-06 CA CA002192850A patent/CA2192850A1/en not_active Abandoned
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4816374A (en) * | 1985-04-12 | 1989-03-28 | Societe D'applications Plastiques Rhone-Alpes (Sapra) | Method of making a plastic material sensitive to laser radiation and enabling it to be marked by a laser, and articles obtained thereby |
Also Published As
Publication number | Publication date |
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BR9508699A (en) | 1997-08-12 |
WO1995034263A1 (en) | 1995-12-21 |
EP0766546A1 (en) | 1997-04-09 |
EP0766546A4 (en) | 1997-09-03 |
ATE201318T1 (en) | 2001-06-15 |
AU2690195A (en) | 1996-01-05 |
ES2157329T3 (en) | 2001-08-16 |
EP0766546B1 (en) | 2001-05-23 |
DE69521045D1 (en) | 2001-06-28 |
CA2192850A1 (en) | 1995-12-21 |
DE69521045T2 (en) | 2001-09-06 |
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