JPS6398418A - Foamed and contracted film - Google Patents
Foamed and contracted filmInfo
- Publication number
- JPS6398418A JPS6398418A JP24468886A JP24468886A JPS6398418A JP S6398418 A JPS6398418 A JP S6398418A JP 24468886 A JP24468886 A JP 24468886A JP 24468886 A JP24468886 A JP 24468886A JP S6398418 A JPS6398418 A JP S6398418A
- Authority
- JP
- Japan
- Prior art keywords
- film
- roughness
- foamed
- foaming
- controlled
- 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.)
- Granted
Links
- 230000003746 surface roughness Effects 0.000 claims abstract description 15
- 229920006300 shrink film Polymers 0.000 claims description 15
- 239000006260 foam Substances 0.000 claims description 8
- 229920005672 polyolefin resin Polymers 0.000 claims description 6
- 238000004439 roughness measurement Methods 0.000 claims 1
- 238000001816 cooling Methods 0.000 abstract description 7
- 238000005187 foaming Methods 0.000 abstract description 7
- 238000009413 insulation Methods 0.000 abstract description 3
- 239000000498 cooling water Substances 0.000 abstract description 2
- 238000001125 extrusion Methods 0.000 abstract description 2
- 229920005989 resin Polymers 0.000 abstract description 2
- 239000011347 resin Substances 0.000 abstract description 2
- 238000004090 dissolution Methods 0.000 abstract 1
- 230000002349 favourable effect Effects 0.000 abstract 1
- 239000004088 foaming agent Substances 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- 235000019592 roughness Nutrition 0.000 description 5
- 230000003139 buffering effect Effects 0.000 description 4
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 239000002666 chemical blowing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 235000014214 soft drink Nutrition 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C61/00—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
- B29C61/003—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor characterised by the choice of material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/04—Polymers of ethylene
- B29K2023/06—PE, i.e. polyethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/10—Polymers of propylene
- B29K2023/12—PP, i.e. polypropylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/04—Condition, form or state of moulded material or of the material to be shaped cellular or porous
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2353/00—Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、清涼飲料ガラス容器等のシュリンクラベル
などに用いられる発泡収縮フィルムに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a foamed shrink film used for shrink labels for glass soft drink containers and the like.
(従来技術とその問題点〕
シュリンクラベルは、ポリエチレンなどの発泡倍率2〜
3倍程度の熱収縮性の樹脂フィルムからなり、その一方
の面には品名、販売者等を表示するための印刷が行われ
ており、これを筒状に巻回し、ガラス容器に挿通し、加
熱して収縮させることによりガラス容器に密着させて使
用に供される。(Prior art and its problems) Shrink labels are made of polyethylene with an expansion ratio of 2 to
It is made of a heat-shrinkable resin film that is about 3 times the size, and one side is printed to display the product name, seller, etc., and is rolled into a cylinder and inserted into a glass container. By heating and shrinking it, it is brought into close contact with a glass container for use.
このシュリンクラベルは、発泡フィルムからなるので機
械的な緩衝効果と保温断熱性を有し、特に炭酸飲料など
の清涼飲料水を収容するガラス製容器などの包装材料と
して好適なものである。Since this shrink label is made of a foamed film, it has a mechanical buffering effect and a heat-insulating property, and is particularly suitable as a packaging material for glass containers and the like containing soft drinks such as carbonated drinks.
ところで、このようなシュリンクラベルに用いられる発
泡収縮フィルムにあっては、緩衝効果および保温断熱性
を十分に得ようとすると、発泡倍率を高めることが必要
になる。ところが、発泡倍率を高めるとフィルム表面の
表面粗さが大きくなって、粗面となり、印刷仕上り状態
、特に鮮明性が、大きく低下し、意匠性に欠けると云う
不都合が生じる。逆に、印刷性を高めようとして発泡イ
8率を小さくすると、緩衝効果、保温断熱性が4−分に
得られないと云う不都合が生じる。By the way, in the case of a foamed shrink film used for such a shrink label, in order to obtain sufficient buffering effect and heat-insulating properties, it is necessary to increase the foaming ratio. However, when the expansion ratio is increased, the surface roughness of the film surface increases, resulting in a rough surface, resulting in a significant decrease in print finish, especially sharpness, and a lack of design. On the other hand, if the foaming ratio is reduced in an attempt to improve printability, there arises the disadvantage that the buffering effect and heat-insulating properties cannot be obtained within 4 minutes.
そこでこの発明にあっては、ポリオレフィン系樹脂から
なる発泡収縮フィルムにおいて、表裏面の粗さを10〜
20μ雇の間とするとともに表面の粗さをA、裏面の粗
さをBとすると
にして、上記相反する問題を解決するようにした。Therefore, in this invention, in a foam shrink film made of polyolefin resin, the roughness of the front and back surfaces is set to 10 to 10.
The above-mentioned conflicting problems were solved by setting the surface roughness to be 20 μm, and the surface roughness to be A, and the back surface roughness to B.
この発明における発泡収縮フィルムの表面粗さの測定は
、JIS−B−0601で規定される方法によって行わ
れる。具体的には、触針式(JIS−8−0651)、
平均アラサ直読式(JIS−B−0655) 、光切断
式(JIS−8−0653) 、光波干渉式(JIS−
8−0652) 、N Fアラサ式(JIS−8’−0
656)などを用いることができる。The surface roughness of the foamed shrink film in this invention is measured by the method specified in JIS-B-0601. Specifically, stylus type (JIS-8-0651),
Average roughness direct reading type (JIS-B-0655), optical cutting type (JIS-8-0653), light wave interference type (JIS-
8-0652), NF rough type (JIS-8'-0
656) etc. can be used.
発泡収縮フィルムの両面の粗さの絶対値が10μm未満
では発泡倍率を低くぜざるを得ず、断熱保温性、緩衝効
果が不十分である。また、20μmを越えると印刷性が
表面、裏面ともに低下し、鮮明な印刷が行えなくなる。If the absolute value of the roughness on both sides of the foam shrink film is less than 10 μm, the foaming ratio must be low, resulting in insufficient heat insulation and buffering effects. Furthermore, if the thickness exceeds 20 μm, printability deteriorates on both the front and back surfaces, making it impossible to print clearly.
また、A−B が0.1より未満であると、表面の粗
さが十分小さくならず、印刷面として不適であり、裏面
の粗さが十分に大きくならず、緩衝性、保温断熱性で不
利となる。したがって、この発明の発泡収縮フィルムの
平均発泡倍率は約1.5〜2.0倍の範囲となる。In addition, if A-B is less than 0.1, the surface roughness will not be sufficiently small, making it unsuitable as a printing surface, and the back surface roughness will not be sufficiently large, resulting in poor cushioning and heat-insulating properties. It will be disadvantageous. Therefore, the average expansion ratio of the foam shrinkage film of the present invention is in the range of about 1.5 to 2.0 times.
また、延伸倍率は3.5〜5.0倍の範囲が好適となる
。Further, the stretching ratio is preferably in the range of 3.5 to 5.0 times.
このような発泡収縮フィルムでは、表裏面の粗さが異な
り、一方の面は比較的平滑で印刷性に適し、他方の面は
比較的粗く、緩衝性が高く、保温断熱性が優れたものと
なる。In this type of foam shrink film, the front and back surfaces have different roughness, one side is relatively smooth and suitable for printing, and the other side is relatively rough and has high cushioning properties and excellent heat and insulation properties. Become.
次に、このような発泡収縮フィルムの製法について説明
する。Next, a method for manufacturing such a foam shrink film will be explained.
まず、ポリオレフィン系樹脂を用意する。ポリオレフィ
ン系樹脂としては、低密度ポリエチレン、高密度ポリエ
チレン、ポリプロピレン、エチレンープロピレンブロッ
クコボリマー、エチレン−プロピレンランダムコポリマ
ーなどやこれらのブレンドポリマーなどが用いられる。First, a polyolefin resin is prepared. As the polyolefin resin, low density polyethylene, high density polyethylene, polypropylene, ethylene-propylene block copolymer, ethylene-propylene random copolymer, and blend polymers thereof are used.
これらのポリオレフィン系樹脂にアソビスイソブチロニ
トリル、アゾジカルボンアミド、N、N’ −ジニトロ
ソペンタメチレンテトラミンなどの化学発泡剤を0.1
〜1,5重量%添加する。これ以外に酸化防止剤、滑剤
、可塑剤、帯電防止剤などの添加剤を必要に応じて所要
量添加することができる。A chemical blowing agent such as azobisisobutyronitrile, azodicarbonamide, or N,N'-dinitrosopentamethylenetetramine is added to these polyolefin resins at 0.1
Add ~1.5% by weight. In addition, additives such as antioxidants, lubricants, plasticizers, and antistatic agents may be added in required amounts as necessary.
この混合物をヘンシェルミキサー、タンブラ−などの混
合機によって均一にトライブレンドして樹脂組成物とす
る。This mixture is homogeneously triblended using a mixer such as a Henschel mixer or a tumbler to obtain a resin composition.
ついで、この樹脂組成物を押出機を用いるインフレーシ
ョン法やT−ダイ法などによって溶融押出してフィルム
化するとともに発泡させる。この成形の際、押出ダイス
直後で吐出された溶融状フィルムの片面のみに小径の冷
却ロールを接触させるか、あるいはこのフィルムの片面
にのみ少量の冷却水を噴射するなどの手段により、フィ
ルム片面のみを予備冷却する。この予備冷却によってフ
ィルム片面側の発泡セルの生長および化学発泡剤の分解
が抑制され、発泡が抑制された状態となるついで、この
状態のフィルムは、冷却ロール等で冷却されたうえ、延
伸加工されて発泡収縮フィルムが得られる。Next, this resin composition is melt-extruded to form a film and foamed by an inflation method using an extruder, a T-die method, or the like. During this forming process, only one side of the film can be formed by contacting only one side of the molten film immediately after the extrusion die with a small-diameter cooling roll, or by spraying a small amount of cooling water only on one side of the film. Pre-cool. This preliminary cooling suppresses the growth of foam cells on one side of the film and the decomposition of the chemical blowing agent, resulting in a state where foaming is suppressed.The film in this state is then cooled with a cooling roll, etc., and then stretched. A foamed shrink film is obtained.
このような製法により、表面と裏面とで発泡倍率が異な
り、表面粗さが異なるフィルムが得られ、フィルム片側
の予備冷却の度合を調節することにるフィルムを得るこ
とができる。By such a manufacturing method, it is possible to obtain a film in which the front and back surfaces have different expansion ratios and different surface roughnesses, and it is possible to obtain a film in which the degree of preliminary cooling on one side of the film can be adjusted.
以下、実施例を示して作用、効果を明確にする。 Hereinafter, examples will be shown to clarify the functions and effects.
種々のポリオレフィン系樹脂を用いて、押出機のダイス
直後の溶融フィルムの片面にのみ冷却ロールを接触させ
る方法により、この発明の発泡収縮フィルムを得た。こ
の発泡収縮フィルムについて、機械方向の収縮率が40
%となる温度(40%収縮温度)、表面粗さ、印刷仕上
り、保温性について測定した。40%収縮温度は、各温
度における機械方向の熱収縮率をJIS−Z−1709
にしたがって測定し、収縮率が40%の時の温度をグラ
フから求めた。表面粗さは、■小成研究所製5E−3C
万能
平均粗さ法により求めた。印刷仕上りは、肉眼で観察し
、その評価を下記のように行った。The foamed shrink films of the present invention were obtained using various polyolefin resins by a method in which a cooling roll was brought into contact with only one side of the molten film immediately after the extruder die. This foamed shrink film has a shrinkage rate of 40 in the machine direction.
% temperature (40% shrinkage temperature), surface roughness, print finish, and heat retention properties were measured. The 40% shrinkage temperature is the heat shrinkage rate in the machine direction at each temperature according to JIS-Z-1709.
The temperature was determined from the graph when the shrinkage rate was 40%. The surface roughness is ■5E-3C manufactured by Kosei Research Institute
It was determined by the universal average roughness method. The print finish was visually observed and evaluated as follows.
◎:非常に良好
○:良 好
Δ:やや不良
×:不 良
保温性は容量300dのガラス容器にこのフィルムを巻
き、収縮させ、水を充填して70℃の恒温槽に1時間放
置後、取り出し、ガラス容器のフィルム部分を手で持っ
た時の熱の感じ方で評価した。◎: Very good ○: Good Δ: Slightly poor ×: Poor Heat retention was determined by wrapping this film around a glass container with a capacity of 300 d, shrinking it, filling it with water, and leaving it in a constant temperature bath at 70°C for 1 hour. It was evaluated by how hot it felt when the film part of the glass container was taken out and held in the hand.
○:1分以分子上手てる。○: Molecular success for more than 1 minute.
△:30秒以内なら手で持てる。△: Can be held in hand for less than 30 seconds.
×:10秒以内なら手で持てる。×: Can be held in hand for less than 10 seconds.
比較として、従来の予備冷却しない方法で製造した発泡
収縮フィルムについても同様の検討を行った。For comparison, a similar study was conducted on a foam shrink film produced using a conventional method without pre-cooling.
結果を別表に併せて示す。The results are also shown in the attached table.
別表の結果から明らかなように、この発明の発泡収縮フ
ィルムは良好な印刷性と保温性とを兼ね備えていること
がわかる。As is clear from the results in the attached table, the foamed shrink film of the present invention has both good printability and heat retention.
以上説明したように、この発明の発泡収縮フィルムは、
1枚のフィルムの一方の面が比較的平滑となり、他方の
面が比較的粗くなるので、平滑面は印刷適性が良好とな
り、粗面側は保温性、緩衝性を十分保持するものとなる
。As explained above, the foamed shrink film of the present invention is
Since one side of one film is relatively smooth and the other side is relatively rough, the smooth side has good printability, and the rough side has sufficient heat retention and cushioning properties.
よって、この発泡収縮フィルムは、例えばワンウェイ容
器などのシリンクラベルなどに好適なものとなる。Therefore, this foamed shrink film is suitable for, for example, shrink labels for one-way containers and the like.
Claims (1)
て、 このフィルムの表面の粗さをA、裏面の粗さをBとする
と、 AおよびBは10〜20μmであり、 かつ(A−B/A)≧0.1である(粗さ測定はJIS
−B−0601による。)ことを特徴とする発泡収縮フ
ィルム。[Claims] In a foam shrinkable film made of a polyolefin resin, where the surface roughness of the film is A and the back surface roughness is B, A and B are 10 to 20 μm, and (A-B /A) ≧0.1 (roughness measurement is JIS
- According to B-0601. ) A foam shrink film characterized by:
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24468886A JPS6398418A (en) | 1986-10-15 | 1986-10-15 | Foamed and contracted film |
US07/105,431 US4740529A (en) | 1986-01-07 | 1987-01-07 | Heat resistant foamed shrinkable film |
PCT/JP1987/000009 WO1990005758A1 (en) | 1986-01-07 | 1987-01-07 | Heat-resistant foam-shrinkable film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24468886A JPS6398418A (en) | 1986-10-15 | 1986-10-15 | Foamed and contracted film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6398418A true JPS6398418A (en) | 1988-04-28 |
JPH0560413B2 JPH0560413B2 (en) | 1993-09-02 |
Family
ID=17122461
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24468886A Granted JPS6398418A (en) | 1986-01-07 | 1986-10-15 | Foamed and contracted film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6398418A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005241157A (en) * | 2004-02-27 | 2005-09-08 | Kyoraku Co Ltd | Foam duct |
WO2007034884A1 (en) * | 2005-09-22 | 2007-03-29 | Nissei Industrial Co., Ltd. | Foamed film for shrink labels |
JP2010203772A (en) * | 2010-06-25 | 2010-09-16 | Kyoraku Co Ltd | Foam duct |
-
1986
- 1986-10-15 JP JP24468886A patent/JPS6398418A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005241157A (en) * | 2004-02-27 | 2005-09-08 | Kyoraku Co Ltd | Foam duct |
WO2007034884A1 (en) * | 2005-09-22 | 2007-03-29 | Nissei Industrial Co., Ltd. | Foamed film for shrink labels |
JP2007084696A (en) * | 2005-09-22 | 2007-04-05 | Nissei Kagaku Kk | Foamed film for shrinkable label |
JP2010203772A (en) * | 2010-06-25 | 2010-09-16 | Kyoraku Co Ltd | Foam duct |
Also Published As
Publication number | Publication date |
---|---|
JPH0560413B2 (en) | 1993-09-02 |
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