WO1986003767A1 - Marking materials - Google Patents
Marking materials Download PDFInfo
- Publication number
- WO1986003767A1 WO1986003767A1 PCT/US1985/002442 US8502442W WO8603767A1 WO 1986003767 A1 WO1986003767 A1 WO 1986003767A1 US 8502442 W US8502442 W US 8502442W WO 8603767 A1 WO8603767 A1 WO 8603767A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- marking
- base
- air permeability
- pore size
- marking material
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 54
- 230000035699 permeability Effects 0.000 claims abstract description 24
- 239000011148 porous material Substances 0.000 claims abstract description 19
- 239000012790 adhesive layer Substances 0.000 claims abstract description 11
- 239000002985 plastic film Substances 0.000 claims abstract description 5
- 229920006255 plastic film Polymers 0.000 claims abstract description 5
- 238000011156 evaluation Methods 0.000 description 11
- 239000010410 layer Substances 0.000 description 7
- 238000010276 construction Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- -1 polyethylene Polymers 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000003522 acrylic cement Substances 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 238000010943 off-gassing Methods 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 230000000007 visual effect Effects 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
- C09J7/26—Porous or cellular plastics
-
- 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
- G09F2003/023—Adhesive
- G09F2003/0236—Permeability
Definitions
- This invention relates to an improvement in marking materials for decoration and marking used by application to outdoor signs, gasoline tanks for two-wheeled vehicles, vehicular body surfaces and the like. More particularly, this invention relates to an improvement in air-permeable marking materials without causing peeling or blistering, etc. even on evolution of gases (outgassing) from the adherend to be applied.
- Figures 3 to 7 are sectional views illustrating conventional air-permeable marking materials wherein 1 is the base; 2 is the adhesive layer; 3 is a hole; 4 is a porous layer; 5 is the adherend; and 6 is the marking.
- a marking material shown in Figure 3 has a construction wherein an adhesive layer 2 is laminated to a base 1, and venting holes 3 are mechanically or chemically formed therein.
- a marking material as shown in Figure 4 has a construction, wherein a base 1 is formed from an air-permeable fibrous material.
- a marking material as shown in Figure 5 has a construction wherein an air-permeable porous layer 4 such as a foam, paper or fibrous material is formed between a base 1 and an adhesive layer 2. (See for example the laid-open publication of Japanese UM application Kokai (laid-Open) No. 90980/84).
- a marking material as shown in Figure 6 has a construction wherein an adhesive layer 2 is formed from an expanded porous material.
- an air-impermeable marking material having a construction wherein a base 1 is extremely thick (about 250 ⁇ m or above) and the strength thereof is increased to enclose an escaping gas .
- a desired marking is provided on the marking material of Figure 3 and has too large a pore size (usually formed by printing methods such as offset, gravure or screen printing, or coating methods such as roll coating or knife coating) , the surface conditions are bad with poor gloss, and the marking material cannot be put to vertical use. If the pore size is too small, pores are filled in forming the marking, and the air permeability is unfavorably inferior. The working of pore size is very difficult with bad workability.
- the base 1 has low mechanical strength and is easily broken.
- the smoothness of the base 1 is poor, and it is difficult to obtain a glossy marking material.
- the marking material shown in Figure 5 has porous layer 4 of low mechanical strength which not only tends to cause layer cleavage but also is incapable of outgassing outside, thereby causing blistering, etc. on application to an adherend evolving a great volume of gases (for example application to molded RIM bumpers or FRP plates or application to polyethylene containers filled with gasoline).
- the marking material shown in Figure 6 not only has a low bonding strength and tends to peel from the adherend but also is incapable of letting a large volume of gases escape to the outside, thereby causing blistering, - etc. in the same manner as the marking material shown in Figure 5.
- the marking material shown in Figure 7 arouses no problem in a short time after application to an adherend, but there is a problem of rather severe blistering, peeling, etc. with the lapse of time.
- a marking material comprising an adhesive layer on at least one surface of a base, said base being formed from a continuous porous plastic film having an average pore size of 0.2 to 50 ⁇ m, an air permeability of 2 to 120 sec/100 cc and a thickness of at least 20 ⁇ m.
- Figure 1 is a sectional view showing the marking material of this invention
- Figure 2 is a sectional view of a marking material of this invention, which is given marking and applied to an adherend;
- Figures 3 to 7 are sectional views illustrating conventional air-permeable marking materials wherein:
- 2 is the adhesive layer; 3 is a hole;
- Such materials have a construction wherein a base 1 is formed from a continuous porous plastic film having an average pore size of 0.2 to 50 ⁇ m, an air permeability of 2 to 120 sec/100 cc (measured by the Gurley method provided for in the JIS P8117) and a thickness of at least 20 ⁇ m, and an adhesive layer 2 contained on one side of the base 1.
- a release material may be further laminated to the surface of the adhesive layer 2 to facilitate the handling of the marking materials. If the average pore size is smaller than 0.2 ⁇ m, the holes are filled by the marking formed on the marking materials, and the air permeability is unfavor ⁇ ably inferior.
- the average pore ' size exceeds 50 ⁇ m, poor appearance of the marking is produced, and the material cannot be placed into practical use.
- the average pore size within the range of 20 to 20 ⁇ m is particularly preferred for providing glossy marking while obtaining effective air permeability. If the air permeability (measured in sec/100 cc by the Gurley method provided for in the JIS P8117) exceeds 2 sec/100 cc (the lower value meaning a greater air permeability, and the value exceeding 2 sec/100 cc meaning a smaller value, the surface smoothness of the base 1 is inferior, and poor appearance of the marking is produced. If the air permeability is below 120 sec/100 cc (the numerical value is increased in this case), the air permeability is unfavorably inferior.
- the air perme ⁇ ability of 10 to 50 sec/100 cm is more preferred, considering the strength and air permeability performance of the base 1.
- the thickness of the base 1 is below 20 ⁇ m, the area of th cut end surface of the marking materials is small, and the air permeability will be unfavorably inferior.
- the thickness of the base 1 is preferably in the range of 60 to 200 ⁇ m taking into account the stabilized air permeability, economic efficiency and workability, etc. of the marking materials.
- the base 1 of this invention can be produced by the respective methods of sintering, mixed extracting, phase separation and drawing as disclosed in the post-exam publication of Japanese Patent Kokoku (Post-Exam Publn.) No. 5327/84 and the like, and general-purpose thermoplastic materials such as vinyl chloride, polyethylene, acrylic, urethane and polypropy- lene may be used.
- An adhesive capable of providing sufficient adhesive force to the base to be laminated to the adherend may be sufficiently used, and a coating thickness within the ordinarily used range provides sufficient air permeability without performing working. Therefore, a general-purpose adhesive such as acrylic, rubber, silicone and the like may be used.
- the marking surface of the marking material similar to the above-mentioned (a) was inspected by visual examination, and evaluation was made on the following criteria:
- Table 1 shows evaluation results of tests with varying average pore size at a base thickness of 70 ⁇ m and an air permeability of 30 sec/100 cc.
- Table 2 shows evaluation results of tests with varying air permeability at a base thickness of 70 ⁇ m and an average pore size of 10 um.
- Table 3 shows evaluation results of tests with varying base thickness at an average base pore size of 10 ⁇ m and an air permeability of 30 sec/100 cc.
- Results x were obtained in both the blistering tests 1 and 2 of the conventional marking materials shown in Figures 3, 5, 6 and 7 cited above, and results x were obtained in the appearance conditions of the conventional marking material shown in Figure 4 cited above. Table 2
- Example 2 A continuous porous polypropylene film (manufactured by Sumitomo 3M Ltd.) was used as a base, and the surface of the base was primed with a chlorinated polypropylene (manufactured by Toyo Kasei Kogyo Co., Ltd.). An acrylic adhesive and a release material were laminated to the primed base similarly to Example 1 to form a marking material. Marking was provided on the base in the manner similar to Example 1, and evaluation of the aforesaid blistering tests (respectively collected in one mark since similar results were obtained in (T) and( ⁇ 2)) , appearance conditions and surface gloss was made. Evaluation results of this Example and a Comparative Example are shown in Tables 4 to 6.
- Table 4 shows evaluation results of tests with varying average pore size at a base thickness of 80 ⁇ m and an air permeability of 38 sec/100 cc.
- Table 5 shows evaluation results of tests with varying air permeability at a base thickness of 80 ⁇ m and an average pore size of 3.2 ⁇ m.
- Table 6 shows evaluation results of tests with varying base thickness at an average base pore size of 3.2 ⁇ m and an air permeability o 38 sec/100 cc.
- the base of the marking materials of this invention is formed from a continuous porous plastic film having an average pore size of 0.2 to 50 ⁇ m, an air permeability of 2-120 sec/100 cc and a thickness of 20 ⁇ m or above, and marking having good matte to glossy appearance conditions can be provided on the base. Furthermore, a marking material having sufficient air permeability can be obtained even if marking is provided all over the surface. Since there is no porous layer between the base and the adhesive layer, the marking materials having a high strength can be provided without causing layer cleavage.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Theoretical Computer Science (AREA)
- Adhesive Tapes (AREA)
- Laminated Bodies (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Glass Compositions (AREA)
- General Preparation And Processing Of Foods (AREA)
Abstract
A marking material comprising an adhesive layer on at least one surface of a base, the base comprising a continuous porous plastic film having an average pore size of 0.2 to 50 gammam, an air permeability of 2 to 120 sec/100 cc and a thickness of at least 20 mum.
Description
MARKING MATERIALS
Technical Field
This invention relates to an improvement in marking materials for decoration and marking used by application to outdoor signs, gasoline tanks for two-wheeled vehicles, vehicular body surfaces and the like. More particularly, this invention relates to an improvement in air-permeable marking materials without causing peeling or blistering, etc. even on evolution of gases (outgassing) from the adherend to be applied.
Background Art Prior art air-permeable marking materials are explained by referring to Figures 3 to 7 wherein Figures 3 to 7 are sectional views illustrating conventional air-permeable marking materials wherein 1 is the base; 2 is the adhesive layer; 3 is a hole; 4 is a porous layer; 5 is the adherend; and 6 is the marking.
A marking material shown in Figure 3 has a construction wherein an adhesive layer 2 is laminated to a base 1, and venting holes 3 are mechanically or chemically formed therein.
A marking material as shown in Figure 4 has a construction, wherein a base 1 is formed from an air-permeable fibrous material. A marking material as shown in Figure 5 has a construction wherein an air-permeable porous layer 4 such as a foam, paper or fibrous material is formed between a base 1 and an adhesive layer 2. (See for example the laid-open publication of Japanese UM application Kokai (laid-Open) No. 90980/84).
A marking material as shown in Figure 6 has a construction wherein an adhesive layer 2 is formed from an expanded porous material.
Furthermore, as shown in Figure 7, there is an air-impermeable marking material having a construction wherein a base 1 is extremely thick (about 250 μm or
above) and the strength thereof is increased to enclose an escaping gas .
If a desired marking is provided on the marking material of Figure 3 and has too large a pore size (usually formed by printing methods such as offset, gravure or screen printing, or coating methods such as roll coating or knife coating) , the surface conditions are bad with poor gloss, and the marking material cannot be put to vertical use. If the pore size is too small, pores are filled in forming the marking, and the air permeability is unfavorably inferior. The working of pore size is very difficult with bad workability.
In the marking material shown in Figure 4, the base 1 has low mechanical strength and is easily broken. The smoothness of the base 1 is poor, and it is difficult to obtain a glossy marking material.
The marking material shown in Figure 5 has porous layer 4 of low mechanical strength which not only tends to cause layer cleavage but also is incapable of outgassing outside, thereby causing blistering, etc. on application to an adherend evolving a great volume of gases (for example application to molded RIM bumpers or FRP plates or application to polyethylene containers filled with gasoline). The marking material shown in Figure 6 not only has a low bonding strength and tends to peel from the adherend but also is incapable of letting a large volume of gases escape to the outside, thereby causing blistering, - etc. in the same manner as the marking material shown in Figure 5.
The marking material shown in Figure 7 arouses no problem in a short time after application to an adherend, but there is a problem of rather severe blistering, peeling, etc. with the lapse of time.
Summary of the Invention
In accordance with the invention, there is provided a marking material comprising an adhesive layer
on at least one surface of a base, said base being formed from a continuous porous plastic film having an average pore size of 0.2 to 50 μm, an air permeability of 2 to 120 sec/100 cc and a thickness of at least 20 μm. Thus, the object of this invention is to provide marking materials to which a marking of good appearance conditions can be given without causing problems of peeling, blistering, etc. even on application to adherends evolving a great volume of gases.
Brief Description of the Drawings
Figure 1 is a sectional view showing the marking material of this invention;
Figure 2 is a sectional view of a marking material of this invention, which is given marking and applied to an adherend;
Figures 3 to 7 are sectional views illustrating conventional air-permeable marking materials wherein:
1 is the base;
2 is the adhesive layer; 3 is a hole;
4 is a porous layer;
5 is the adherend; and
6 is the marking.
Detailed Description Marking materials of this invention are explained by referring to Figure 1. Such materials have a construction wherein a base 1 is formed from a continuous porous plastic film having an average pore size of 0.2 to 50 μm, an air permeability of 2 to 120 sec/100 cc (measured by the Gurley method provided for in the JIS P8117) and a thickness of at least 20 μm, and an adhesive layer 2 contained on one side of the base 1. A release material may be further laminated to the surface of the adhesive layer 2 to facilitate the handling of the marking materials.
If the average pore size is smaller than 0.2 μm, the holes are filled by the marking formed on the marking materials, and the air permeability is unfavor¬ ably inferior. If the average pore' size exceeds 50 μm, poor appearance of the marking is produced, and the material cannot be placed into practical use. The average pore size within the range of 20 to 20 μm is particularly preferred for providing glossy marking while obtaining effective air permeability. If the air permeability (measured in sec/100 cc by the Gurley method provided for in the JIS P8117) exceeds 2 sec/100 cc (the lower value meaning a greater air permeability, and the value exceeding 2 sec/100 cc meaning a smaller value, the surface smoothness of the base 1 is inferior, and poor appearance of the marking is produced. If the air permeability is below 120 sec/100 cc (the numerical value is increased in this case), the air permeability is unfavorably inferior. The air perme¬ ability of 10 to 50 sec/100 cm is more preferred, considering the strength and air permeability performance of the base 1.
In the case of marking 6 provided on the whole surface of the marking materials as shown in Figure 2, a number of holes on the surface of the marking materials are filled by the marking 6 (ink or clear coating) to thus reduce the air permeability. However, an escaping gas A evolved from the adherend escapes even from the cut end surfaces of the marking materials. If the thickness of the base 1 is below 20 μm, the area of th cut end surface of the marking materials is small, and the air permeability will be unfavorably inferior. The thickness of the base 1 is preferably in the range of 60 to 200 μm taking into account the stabilized air permeability, economic efficiency and workability, etc. of the marking materials. The base 1 of this invention can be produced by the respective methods of sintering, mixed extracting, phase separation and drawing as disclosed in the
post-exam publication of Japanese Patent Kokoku (Post-Exam Publn.) No. 5327/84 and the like, and general-purpose thermoplastic materials such as vinyl chloride, polyethylene, acrylic, urethane and polypropy- lene may be used.
An adhesive capable of providing sufficient adhesive force to the base to be laminated to the adherend may be sufficiently used, and a coating thickness within the ordinarily used range provides sufficient air permeability without performing working. Therefore, a general-purpose adhesive such as acrylic, rubber, silicone and the like may be used.
Examples The marking materials of this invention are described in more detail by way of the following non-limiting examples.
Example 1
To a vinyl chloride organosol (manufactured by
Sumitomo 3M Ltd.), was added 20% by weight of ethyl alcohol, and the resulting mixture was stirred with a propeller mixer at 800 rpm for 15 min. The stirred mixture was cast to form a continuous porous base by the phase separation method. An acrylic adhesive having a dry thickness of 30 μm (manufactured by Sumitomo 3M Ltd. ) and a release material were laminated to base 1 to form a marking material. The whole base surface of the resulting marking material was printed with a #3900 series ink manufactured by Sumitomo 3M Ltd. by screen printing.
After drying, the printing was similarly coated with "Clear Coating GA-11® manufactured by Sumitomo 3M Ltd. to a dry thickness of about 10 μm. The resultant marking material was used to carry out the following tests:
(a) Blistering test l) A 500-cc wide-mouthed polyethylene bottle manufactured by Sanko Plastic K.K. was filled with
gasoline, and sealed, followed by application of the above-mentioned material to the surface of the bottle. The marking material was allowed to stand at 25 C and 65% RH for one month, and inspected visually for blistering. (2) The above-mentioned marking material was applied to an RIM molded article of an automobile bumper (manufactured by Mitsubishi Belting Ltd.) within 24 hours after molding. The resulting molded article was placed in an oven at 80 C for 48 hours and then inspected visually for blistering.
Evaluation was made on the following criteria in both tests(T) and( ).
(g) No occurrence of blistering
Q Occurrence of minute blistering / Occurrence of partial blistering x Occurrence of blistering on the whole surface (b) Appearance conditions
The marking surface of the marking material similar to the above-mentioned (a) was inspected by visual examination, and evaluation was made on the following criteria:
(g) Very glossy
Q Glossy (Good appearance conditions)« Matte x Rough surface (Bad appearance, i.e., without gloss and bad conditions relative to the spread of ink) (c) Surface gloss
Gloss of the marking surface of the marking material similar to the above-mentioned (a) was measured at 60 (a digital gloss meter "VG-2P-D3" manufactured by Nippon Denshoku Kogyo Co., Ltd. was used). Results of evaluation of the Example and the
Comparative Example are shown in Tables 1 to 3.
Table 1 shows evaluation results of tests with varying average pore size at a base thickness of 70 μm and an air permeability of 30 sec/100 cc.
Table 2 shows evaluation results of tests with varying air permeability at a base thickness of 70 μm and an average pore size of 10 um.
Table 3 shows evaluation results of tests with varying base thickness at an average base pore size of 10 μm and an air permeability of 30 sec/100 cc.
Table 1
Results x were obtained in both the blistering tests 1 and 2 of the conventional marking materials shown in Figures 3, 5, 6 and 7 cited above, and results x were obtained in the appearance conditions of the conventional marking material shown in Figure 4 cited above.
Table 2
Table 3
Example 2 A continuous porous polypropylene film (manufactured by Sumitomo 3M Ltd.) was used as a base,
and the surface of the base was primed with a chlorinated polypropylene (manufactured by Toyo Kasei Kogyo Co., Ltd.). An acrylic adhesive and a release material were laminated to the primed base similarly to Example 1 to form a marking material. Marking was provided on the base in the manner similar to Example 1, and evaluation of the aforesaid blistering tests (respectively collected in one mark since similar results were obtained in (T) and(~2)) , appearance conditions and surface gloss was made. Evaluation results of this Example and a Comparative Example are shown in Tables 4 to 6.
Table 4 shows evaluation results of tests with varying average pore size at a base thickness of 80 μm and an air permeability of 38 sec/100 cc. Table 5 shows evaluation results of tests with varying air permeability at a base thickness of 80 μm and an average pore size of 3.2 μm. Table 6 shows evaluation results of tests with varying base thickness at an average base pore size of 3.2 μm and an air permeability o 38 sec/100 cc.
Table 4
Table 6
As explained above, the base of the marking materials of this invention is formed from a continuous porous plastic film having an average pore size of 0.2 to
50 μm, an air permeability of 2-120 sec/100 cc and a thickness of 20 μm or above, and marking having good matte to glossy appearance conditions can be provided on the base. Furthermore, a marking material having sufficient air permeability can be obtained even if marking is provided all over the surface. Since there is no porous layer between the base and the adhesive layer, the marking materials having a high strength can be provided without causing layer cleavage.
Claims
1. Marking material comprising an adhesive layer on at least one surface of a base, said base being formed from a continuous porous plastic film having an average pore size of 0.2 to 50 μm, an air permeability of 2 to 120 sec/100 cc and a thickness of at least 20 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019860700562A KR930010441B1 (en) | 1984-12-14 | 1985-12-10 | Marking materials |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59/262993 | 1984-12-14 | ||
JP59262993A JPS61141477A (en) | 1984-12-14 | 1984-12-14 | Marking material |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1986003767A1 true WO1986003767A1 (en) | 1986-07-03 |
Family
ID=17383405
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1985/002442 WO1986003767A1 (en) | 1984-12-14 | 1985-12-10 | Marking materials |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0203996A1 (en) |
JP (1) | JPS61141477A (en) |
KR (1) | KR930010441B1 (en) |
CA (1) | CA1282287C (en) |
WO (1) | WO1986003767A1 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2645473A1 (en) * | 1989-03-31 | 1990-10-12 | Minnesota Mining & Mfg | APPLICATION TAPE AND TRANSFER ARTICLE COMPRISING SUCH A RIBBON |
WO1995027014A1 (en) * | 1994-04-04 | 1995-10-12 | Minnesota Mining And Manufacturing Company | Microparticle-containing pressure sensitive adhesive tape |
US5512612A (en) * | 1994-04-04 | 1996-04-30 | Minnesota Mining And Manufacturing Company | Pressure sensitive adhesive employing a water-dispersible polymer and articles made there from |
WO2002067592A1 (en) * | 2001-02-21 | 2002-08-29 | Sony Corporation | Data transmission method and device |
WO2002084918A3 (en) * | 2001-04-13 | 2004-12-02 | Nitto Denko Corp | Sealing material for electrical/electronic appliance |
EP1510991A3 (en) * | 2003-08-26 | 2006-01-18 | Nitto Denko Corporation | Label and ventilation housing using the same |
US20150247064A1 (en) * | 2012-09-28 | 2015-09-03 | Lintec Corporation | Adhesive sheet and method for manufacturing adhesive sheet |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0416479U (en) * | 1990-05-31 | 1992-02-10 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3854581A (en) * | 1972-04-10 | 1974-12-17 | Monarch Marking Systems Inc | Pressure-sensitive material and supporting material combination |
FR2288626A1 (en) * | 1974-10-23 | 1976-05-21 | Seilib | Document markers anchored by pressure on adhesive loaded foam - for use on or to anchor various surfaces without damage to the substrate |
US4169184A (en) * | 1973-05-07 | 1979-09-25 | Joseph Pufahl | Adhesive coated impregnated polyurethane foam |
-
1984
- 1984-12-14 JP JP59262993A patent/JPS61141477A/en active Granted
-
1985
- 1985-12-10 WO PCT/US1985/002442 patent/WO1986003767A1/en not_active Application Discontinuation
- 1985-12-10 KR KR1019860700562A patent/KR930010441B1/en not_active Expired - Fee Related
- 1985-12-10 EP EP86900474A patent/EP0203996A1/en not_active Withdrawn
- 1985-12-13 CA CA000497556A patent/CA1282287C/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3854581A (en) * | 1972-04-10 | 1974-12-17 | Monarch Marking Systems Inc | Pressure-sensitive material and supporting material combination |
US4169184A (en) * | 1973-05-07 | 1979-09-25 | Joseph Pufahl | Adhesive coated impregnated polyurethane foam |
FR2288626A1 (en) * | 1974-10-23 | 1976-05-21 | Seilib | Document markers anchored by pressure on adhesive loaded foam - for use on or to anchor various surfaces without damage to the substrate |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2645473A1 (en) * | 1989-03-31 | 1990-10-12 | Minnesota Mining & Mfg | APPLICATION TAPE AND TRANSFER ARTICLE COMPRISING SUCH A RIBBON |
WO1995027014A1 (en) * | 1994-04-04 | 1995-10-12 | Minnesota Mining And Manufacturing Company | Microparticle-containing pressure sensitive adhesive tape |
US5512612A (en) * | 1994-04-04 | 1996-04-30 | Minnesota Mining And Manufacturing Company | Pressure sensitive adhesive employing a water-dispersible polymer and articles made there from |
US5609932A (en) * | 1994-04-04 | 1997-03-11 | Minnesota Mining And Manufacturing Company | Microparticle-containing pressure sensitive adhesive tape |
US5626955A (en) * | 1994-04-04 | 1997-05-06 | Minnesota Mining And Manufacturing Company | Microparticle-containing pressure sensitive adhesive tape |
US5641567A (en) * | 1994-04-04 | 1997-06-24 | Minnesota Mining And Manufacturing Company | Pressure sensitive adhesive(s) and articles(s) |
WO2002067592A1 (en) * | 2001-02-21 | 2002-08-29 | Sony Corporation | Data transmission method and device |
WO2002084918A3 (en) * | 2001-04-13 | 2004-12-02 | Nitto Denko Corp | Sealing material for electrical/electronic appliance |
EP1510991A3 (en) * | 2003-08-26 | 2006-01-18 | Nitto Denko Corporation | Label and ventilation housing using the same |
US20150247064A1 (en) * | 2012-09-28 | 2015-09-03 | Lintec Corporation | Adhesive sheet and method for manufacturing adhesive sheet |
US9752061B2 (en) * | 2012-09-28 | 2017-09-05 | Lintec Corporation | Adhesive sheet and method for manufacturing adhesive sheet |
Also Published As
Publication number | Publication date |
---|---|
KR870700085A (en) | 1987-02-28 |
CA1282287C (en) | 1991-04-02 |
EP0203996A1 (en) | 1986-12-10 |
JPH0431396B2 (en) | 1992-05-26 |
JPS61141477A (en) | 1986-06-28 |
KR930010441B1 (en) | 1993-10-25 |
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