JPH0560413B2 - - Google Patents

Info

Publication number
JPH0560413B2
JPH0560413B2 JP24468886A JP24468886A JPH0560413B2 JP H0560413 B2 JPH0560413 B2 JP H0560413B2 JP 24468886 A JP24468886 A JP 24468886A JP 24468886 A JP24468886 A JP 24468886A JP H0560413 B2 JPH0560413 B2 JP H0560413B2
Authority
JP
Japan
Prior art keywords
film
roughness
foamed
jis
heat
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP24468886A
Other languages
Japanese (ja)
Other versions
JPS6398418A (en
Inventor
Kihachi Shishido
Takao Ookubo
Toshio Taka
Akihiro Hashimoto
Kazuo Yoneda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Resonac Holdings Corp
Original Assignee
Showa Denko KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Showa Denko KK filed Critical Showa Denko KK
Priority to JP24468886A priority Critical patent/JPS6398418A/en
Priority to PCT/JP1987/000009 priority patent/WO1990005758A1/en
Priority to US07/105,431 priority patent/US4740529A/en
Publication of JPS6398418A publication Critical patent/JPS6398418A/en
Publication of JPH0560413B2 publication Critical patent/JPH0560413B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0061Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C61/00Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
    • B29C61/003Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor characterised by the choice of material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/10Polymers of propylene
    • B29K2023/12PP, i.e. polypropylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/04Condition, form or state of moulded material or of the material to be shaped cellular or porous
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2353/00Characterised 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2423/00Characterised 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)

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ユリン
クラベルなどに用いられる発泡収縮フイルムに関
する。 〔従来技術とその問題点〕 シユリンクラベルは、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イルムから
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。 このシユリンクラベルは、発泡フイルムからな
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。 ところで、このようなシユリンクラベルに用い
られる発泡収縮フイルムにあつては、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
率を高めるとフイルム表面の表面粗さが大きくな
つて、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倍率
を小さくすると、緩衝効果、保温断熱性が十分に
得られないと云う不都合が生じる。 〔発明が解決しようとする問題点〕 そこで本発明にあつては、ポリオレフイン系樹
脂からなる発泡収縮フイルムにおいて、表裏面の
粗さを10〜20μm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A−B/A≧0.1とな る関係を満足させるようにして、上記相反する問
題を解決するようにした。 この発明における発泡収縮フイルムの表面粗さ
の測定は、JIS−B−0601で規定される方法によ
つて行われる。具体的には、触針式(JIS−B−
0651)、平均アラサ直読式(JIS−B−0655)、光
切断式(JIS−B−0653)、光波干渉式(JIS−B
−0652)、NFアラサ式(JIS−B−0656)などを
用いることができる。 発泡収縮フイルムの両面の粗さの絶対値が10μ
m未満では発泡倍率を低くせざるを得ず、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。また、A−B/A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。
したがつて、この発明の発泡収縮フイルムの平均
発泡倍率は約1.5〜2.0倍の範囲となる。また、延
伸倍率は3.5〜5.0倍の範囲が好適となる。 このような発泡収縮フイルムでは、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。 次に、このような発泡収縮フイルムの製法につ
いて説明する。 まず、ポリオレフイン系樹脂を用意する。ポリ
オレフイン系樹脂としては、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−プロピレンブロツクコポリマー、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。これらのポ
リオレフイ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。 この混合物をヘンシエルミキサー、タンブラー
などの混合機によつて均一にドライブレンドして
樹脂組成物とする。 ついで、この樹脂組成物を押出機を用いるイン
フレーシヨン法やT−ダイ法などによつて溶融押
出してフイ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
イルムの片面のみに小径の冷却ロールを接触させ
るか、あるいはこのフイ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、フイルム片
面のみを予備冷却する。この予備冷却によつてフ
イ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、この状態のフイルムは、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イ
ルムが得られる。 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イルムが得ら
れ、フイルム片側の予備冷却の度合を調節するこ
とにより、上記関係式;A−B/A≧0.1を満足する フイルムを得ることができる。 〔実施例〕 以下、実施例を示して作用、効果を明確にす
る。 別表に示した4種のポリオレフイン系樹脂(樹
脂タイプA、B、C、D)に重量比1〜1.5%の
発泡剤;アゾジカルボンアミドを添加した混合物
を、500mm巾のTダイを装備した65mm押出機を用
い、成形温度180〜200℃で押出し、ダイ直後の溶
融フイルムの片面にのみ冷却ロールを接触させる
予備冷却によつて厚み400μm、発泡倍率1.4〜2.0
倍の発泡シートを成形した。ついで、この発泡シ
ートを加熱ロール方式の一軸延伸機により延伸温
度115℃で延伸倍率4.0〜4.5倍に延伸して、厚さ
約90〜100μmの発泡収縮フイルムを得た。この
発泡収縮フイルムについて、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にしたがつて測定し、収縮率が40%の
時の温度をグラフから求めた。表面粗さは、(株)小
坂研究所製SE−3C万能表面形状測定器により、
JIS−B−0601−1982 10点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
記のように行つた。 ◎:非常に良好 ○:良好 △:やや不良 ×:不良 保温性は容量300mlのガラス容器にこのフイル
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、ガラス容器のフイル
ム部分を手で持つた時の熱の感じ方で評価した。 ○:1分以上手で持てる。 △:30秒以内なら手で持てる。 ×:10秒以内なら手で持てる。 比較として、従来の予備冷却しない方法で製造
した発泡収縮フイルムについても同様の検討を行
つた。 結果を別表に併せて示す。 別表の結果から明らかなように、この発明の発
泡収縮フイ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。 〔発明の効果〕 以上説明したように、この発明の発泡収縮フイ
ルムは、1枚のフイ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。 よつて、この発泡収縮フイルムは、例えばワン
ウエイ容器などのシリンクラベルなどに好適なも
のとなる。 【表】
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a foamed shrink film used for shrink labels for soft drink glass containers and the like. [Prior art and its problems] Shrink labels are made of a heat-shrinkable resin film, such as polyethylene, with a foaming ratio of about 2 to 3 times, and one side is printed to display the product name, seller, etc. This is done by winding it into a cylindrical shape, inserting it into a glass container, heating it and shrinking it, and then bringing it into close contact with the glass container for use. Since this Shrink label is made of a foamed film, it has a mechanical buffering effect and heat-insulating properties, and is particularly suitable as a packaging material for glass containers containing soft drinks such as carbonated drinks. By the way, in the case of the foamed shrinkage film used for such shrinkable labels, 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 increases, resulting in a rough surface, resulting in a disadvantage that the printed finish, especially the sharpness, is greatly reduced and the design is lacking. On the other hand, if the foaming ratio is reduced in an attempt to improve printability, there arises the disadvantage that sufficient buffering effect and heat-insulating properties cannot be obtained. [Problems to be Solved by the Invention] Therefore, in the present invention, the roughness of the front and back surfaces of the foamed shrink film made of polyolefin resin is set to be between 10 and 20 μm, and the roughness of the front surface is set to A and the back surface is set to have a roughness of A and a back surface. The above conflicting problems were solved by satisfying the relationship A-B/A≧0.1, where B is the roughness of the surface. The surface roughness of the foamed shrink film in this invention is measured by the method specified in JIS-B-0601. Specifically, the stylus type (JIS-B-
0651), average roughness direct reading type (JIS-B-0655), light cutting type (JIS-B-0653), light wave interference type (JIS-B
-0652), NF roughness formula (JIS-B-0656), etc. can be used. The absolute value of the roughness on both sides of the foam shrink film is 10μ
If it is less than m, the foaming ratio has to be lowered, and the insulation and heat retention properties and buffering effects are insufficient. Furthermore, if the thickness exceeds 20 μm, printability deteriorates on both the front and back surfaces, making it impossible to print clearly. Furthermore, if A-B/A is less than 0.1, the surface roughness will not be sufficiently reduced;
It is unsuitable as a printing surface, the roughness of the back surface is not large enough, and it is disadvantageous in terms of cushioning properties and heat insulation properties.
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. Further, the stretching ratio is preferably in the range of 3.5 to 5.0 times. In such a 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. Next, a method for producing such a foam shrink film will be explained. 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. Chemical blowing agents such as azobisisobutyronitrile, azodicarbonamide, and N,N'-dinitrosopentamethylenetetramine are added to these polyolefin resins.
Add 0.1-1.5% by weight. In addition, additives such as antioxidants, lubricants, plasticizers, and antistatic agents may be added in required amounts as necessary. This mixture is uniformly dry-blended using a mixer such as a Henschel mixer or a tumbler to obtain a resin composition. Next, this resin composition is melt-extruded to form a film and foamed by an inflation method or a T-die method using an extruder. During this forming process, a small-diameter cooling roll is brought into contact with only one side of the molten film discharged immediately after the extrusion die, or a small amount of cooling water is injected onto only 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 foaming agent, resulting in a state in which foaming is suppressed. Next, the film in this state is cooled with a cooling roll or the like and then stretched to obtain a foamed shrink film. By such a manufacturing method, a film with different expansion ratios and different surface roughness can be obtained on the front and back sides, and by adjusting the degree of preliminary cooling on one side of the film, the above relational expression; A-B/A≧0.1 can be obtained. It is possible to obtain a film that satisfies the following. [Example] Hereinafter, an example will be shown to clarify the action and effect. A mixture of the four types of polyolefin resins (resin types A, B, C, and D) shown in the attached table with a blowing agent of 1 to 1.5% by weight; It is extruded using an extruder at a molding temperature of 180 to 200°C, and pre-cooled by contacting only one side of the molten film with a cooling roll immediately after the die to a thickness of 400 μm and an expansion ratio of 1.4 to 2.0.
A foam sheet of twice the size was molded. Next, this foamed sheet was stretched using a heated roll type uniaxial stretching machine at a stretching temperature of 115° C. and a stretching ratio of 4.0 to 4.5 times to obtain a foamed shrink film having a thickness of about 90 to 100 μm. For this foamed shrink film, the shrinkage rate in the machine direction is
The temperature at 40% (40% contraction temperature), surface roughness, print finish, and heat retention were measured. 40% shrinkage temperature is the JIS heat shrinkage rate in the machine direction at each temperature.
-Z-1709, and the temperature when the shrinkage rate was 40% was determined from the graph. The surface roughness was measured using an SE-3C universal surface profile measuring device manufactured by Kosaka Laboratory Co., Ltd.
It was determined by JIS-B-0601-1982 10-point average roughness method. The print finish was visually observed and evaluated as follows. ◎: Very good ○: Good △: Slightly poor ×: Poor Heat retention was determined by wrapping this film around a 300ml glass container, shrinking it, filling it with water, leaving it in a constant temperature bath at 70℃ for 1 hour, and then taking it out. The evaluation was based on the feeling of heat when holding the film part of the glass container in your hand. ○: Can be held in hand for more than 1 minute. △: Can be held in hand for up to 30 seconds. ×: Can be held in hand for less than 10 seconds. For comparison, a similar study was conducted on a foamed shrink film produced using a conventional method without pre-cooling. The results are also shown in the attached table. 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. [Effects of the Invention] As explained above, in the foam shrinkage film of the present invention, one side of one film is relatively smooth and the other side is relatively rough, so the smooth surface has good printability. Therefore, the rough side retains sufficient heat retention and cushioning properties. Therefore, this foamed shrink film is suitable for, for example, shrink labels for one-way containers and the like. 【table】

Claims (1)

【特許請求の範囲】 1 ポリオレフイン系樹脂からなる発泡収縮フイ
ルムにおいて、 このフイ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イル
ム。
[Scope of Claims] 1. In a foamed shrink film made of 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 in accordance with JIS-B-0601).
JP24468886A 1986-01-07 1986-10-15 Foamed and contracted film Granted JPS6398418A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP24468886A JPS6398418A (en) 1986-10-15 1986-10-15 Foamed and contracted film
PCT/JP1987/000009 WO1990005758A1 (en) 1986-01-07 1987-01-07 Heat-resistant foam-shrinkable film
US07/105,431 US4740529A (en) 1986-01-07 1987-01-07 Heat resistant foamed 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 JPS6398418A (en) 1988-04-28
JPH0560413B2 true 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)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4822670B2 (en) * 2004-02-27 2011-11-24 キョーラク株式会社 Foam duct
JP4818671B2 (en) * 2005-09-22 2011-11-16 日生化学株式会社 Foam film for shrink labels
JP5372844B2 (en) * 2010-06-25 2013-12-18 キョーラク株式会社 Foam duct

Also Published As

Publication number Publication date
JPS6398418A (en) 1988-04-28

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