JP2002371161A - Low hardness rubber composition - Google Patents

Low hardness rubber composition

Info

Publication number
JP2002371161A
JP2002371161A JP2001182751A JP2001182751A JP2002371161A JP 2002371161 A JP2002371161 A JP 2002371161A JP 2001182751 A JP2001182751 A JP 2001182751A JP 2001182751 A JP2001182751 A JP 2001182751A JP 2002371161 A JP2002371161 A JP 2002371161A
Authority
JP
Japan
Prior art keywords
hardness
rubber composition
rubber
low
peroxide
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.)
Withdrawn
Application number
JP2001182751A
Other languages
Japanese (ja)
Other versions
JP2002371161A5 (en
Inventor
Osamu Ando
理 安藤
Kazuhisa Senda
和久 仙田
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.)
Nok Corp
Original Assignee
Nok Corp
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 Nok Corp filed Critical Nok Corp
Priority to JP2001182751A priority Critical patent/JP2002371161A/en
Publication of JP2002371161A publication Critical patent/JP2002371161A/en
Publication of JP2002371161A5 publication Critical patent/JP2002371161A5/ja
Withdrawn legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Abstract

PROBLEM TO BE SOLVED: To provide a low hardness rubber composition having non-bleeding property, and suitably used as a molding raw material for a sealing material of electric parts such as a secondary battery, fuel cell, condenser. SOLUTION: This peroxide curable low hardness rubber composition consists of 95-30 wt.% EPDM having 10<4> -10<6> order of number-average molecular weight and 5-70 wt.% ethylene/an α-olefin copolymer having 10<3> -10<5> order of number- average molecular weight, and can give a cross-linked molded product having <=50 hardness (Duro A). Since the rubber having a low molecular weight is cured by a peroxide, the rubber composition does not have any bleeding material, and the low hardness rubber having the hardness as low as <=50 Duro A hardness if obtained.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、低硬度ゴム組成物
に関する。更に詳しくは、電気部品シール材の成形材料
などとして好適に用いられる過酸化物架橋性低硬度ゴム
組成物に関する。
The present invention relates to a low-hardness rubber composition. More specifically, the present invention relates to a peroxide-crosslinkable low-hardness rubber composition suitably used as a molding material of a sealing material for electric parts.

【0002】[0002]

【従来の技術】ニッケル水素二次電池、リチウムイオン
二次電池、固体高分子型燃料電池、アルミ電解コンデン
サ、電気二重層型コンデンサ等の電気部品用途に用いら
れるシール材料は、電解液、水蒸気等と直接接触する部
位に装着され、これらの内部液を外部に漏らさないと共
に、外部からの不純物を内部に侵入させないことが必要
である。
2. Description of the Related Art Sealing materials used for electric parts such as nickel metal hydride secondary batteries, lithium ion secondary batteries, polymer electrolyte fuel cells, aluminum electrolytic capacitors, electric double layer capacitors, etc. include electrolytes, water vapor and the like. It is necessary to prevent the internal liquid from leaking to the outside and to prevent impurities from the outside from entering the inside.

【0003】そのため、ガスケット、Oリング、パッキ
ン等のシール材が用いられているが、その場合耐熱性お
よび電気絶縁性を有することに加えて、シール材からの
滲出成分がないこと、シールの耐久性能を左右する耐圧
縮永久歪特性にすぐれていること、シール組込時の面圧
を低くするため材料硬度が低いことなどが要求されてい
る。
For this reason, sealing materials such as gaskets, O-rings and packings are used. In such a case, in addition to heat resistance and electric insulation, there is no oozing component from the sealing material, and the durability of the seal is high. It is required that the material has excellent compression set characteristics that affect the performance, and that the material hardness is low in order to reduce the surface pressure when the seal is assembled.

【0004】従来は、この種用途のガスケットとして、
ポリエチレン、ポリプロピレン等のポリオレフィン系樹
脂やオレフィン系熱可塑性エラストマーが用いられてい
るが、シールの耐久性という点からは不十分であった。
一方、低面圧化を目的として、オレフィン系ゴム材料中
に多量の可塑剤を配合し、低硬度化したものも知られて
いるが、シール系内への可塑剤等の滲出(抽出)という問
題もあり、実際の適用はみられなかった。
Conventionally, as a gasket for this kind of application,
Polyolefin-based resins such as polyethylene and polypropylene and olefin-based thermoplastic elastomers are used, but they are insufficient from the viewpoint of seal durability.
On the other hand, for the purpose of lowering the surface pressure, a large amount of a plasticizer is compounded in an olefin-based rubber material, and those having a reduced hardness are also known. There was a problem and no real application was seen.

【0005】[0005]

【発明が解決しようとする課題】本発明の目的は、低硬
度でしかも非滲出性で、二次電池、燃料電池、コンデン
サ等の電気部品のシール材の成形材料などとして好適に
用いられる低硬度ゴム組成物を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a low-hardness and non-leaching material which is suitably used as a molding material for a sealing material for electric parts such as secondary batteries, fuel cells and capacitors. It is to provide a rubber composition.

【0006】[0006]

【課題を解決するための手段】かかる本発明の目的は、
数平均分子量Mnが104〜106オーダーのEPDM約95〜30重量
%および103〜105オーダーのエチレン・α-オレフィン共
重合ゴム約5〜70重量%よりなり、硬度(Duro A)が50以下
の架橋成形品を与える過酸化物架橋性低硬度ゴム組成物
によって達成される。
SUMMARY OF THE INVENTION The object of the present invention is as follows.
Approximately 95 to 30 weight of EPDM with number average molecular weight Mn of 10 4 to 10 6 order
% And an ethylene / α-olefin copolymer rubber of about 5 to 70% by weight on the order of 10 3 to 10 5 and a peroxide crosslinkable low hardness rubber composition which gives a crosslinked molded article having a hardness (Duro A) of 50 or less. Achieved by

【0007】[0007]

【発明の実施の形態】EPDM(エチレン・プロピレン・ジ
エン3元共重合ゴム)としては、数平均分子量Mnが104
106オーダーの市販品をそのまま用いることができる。
これとブレンドして用いられるエチレン・α-オレフィ
ン共重合ゴムとしては、エチレンにプロピレン、ブテン
-1、ペンテン-1、ヘキセン-1、ヘプテン-1、オクテン-1
等のα-オレフィンの少くとも一種を共重合させたMnが1
03〜105オーダーのゴム状共重合体であって、好ましく
はエチレン-プロピレン共重合ゴム(EPR)が用いられる。
DESCRIPTION OF THE PREFERRED EMBODIMENTS EPDM (ethylene-propylene-diene terpolymer rubber) has a number average molecular weight Mn of 10 4 or more.
Commercial products on the order of 10 6 can be used as they are.
Ethylene / α-olefin copolymer rubber used by blending with propylene
-1, pentene-1, hexene-1, heptene-1, octene-1
Mn obtained by copolymerizing at least one α-olefin such as
0 3 to 105 a rubbery copolymer of order, preferably ethylene - propylene copolymer rubber (EPR) is used.

【0008】EPDMとエチレン・α-オレフィン共重合ゴ
ムとは、前者が約95〜30重量%、好ましくは約90〜60重
量%の割合で、また後者が約5〜70重量%、好ましくは約1
0〜40重量%の割合でブレンドして用いられる。後者のブ
レンド割合がこれよりも少ないと、硬さが目的とする50
以下とはならず、一方これ以上の割合でブレンドして用
いられると、混練時にゴムの粘着が激しくなり、均一な
ゴムコンパウンドにまとめることができなくなる。ま
た、これらの各ブレンドゴム成分のMnが、それぞれ上記
範囲に限定されるのも、必要な可塑化効果を得るためで
ある。
[0008] EPDM and ethylene / α-olefin copolymer rubber are used in a proportion of about 95 to 30% by weight, preferably about 90 to 60% by weight, and about 5 to 70% by weight, preferably about 1
It is used by blending at a ratio of 0 to 40% by weight. If the blending ratio of the latter is lower, the hardness is
On the other hand, if the rubber is blended at a higher ratio and used, the rubber becomes strongly adhered at the time of kneading, making it impossible to form a uniform rubber compound. Further, the reason why Mn of each of these blend rubber components is limited to the above range is to obtain a necessary plasticizing effect.

【0009】ブレンドゴムは、それの100重量部当り約
0.2〜10重量部、好ましくは約0.5〜8重量部の割合で用
いられる有機過酸化物によって架橋される。有機過酸化
物としては、一般に用いられているベンゾイルパーオキ
サイド、ジ第3ブチルパーオキサイド、ジクミルパーオ
キサイド、第3ブチルクミルパーオキサイド、1,3-ジ(第
3ブチルパーオキシ)イソプロピルベンゼン、2,5-ジメチ
ル-2,5-ジ(第3ブチルパーオキシ)ヘキサン、2,5-ジメチ
ル-2,5-ジ(第3ブチルパーオキシ)ヘキシン-3、m-トレイ
ルパーオキサイド、ジプロピオニルパーオキサイド等が
用いられる。
[0009] The blended rubber is used in an amount of about 100 parts by weight thereof.
It is crosslinked by an organic peroxide used in a proportion of 0.2 to 10 parts by weight, preferably about 0.5 to 8 parts by weight. Examples of the organic peroxide include commonly used benzoyl peroxide, di-tert-butyl peroxide, dicumyl peroxide, tert-butyl cumyl peroxide, 1,3-di (
(3-butylperoxy) isopropylbenzene, 2,5-dimethyl-2,5-di (tert-butylperoxy) hexane, 2,5-dimethyl-2,5-di (tert-butylperoxy) hexyne-3, m-Trail peroxide, dipropionyl peroxide and the like are used.

【0010】以上の各成分を必須成分とする組成物の調
製は、得られるゴム加硫成形品の硬さDuro Aが20〜50と
なるのを阻害しない範囲内で、ゴムの配合剤として一般
に用いられている2価金属の酸化物または水酸化物より
なる受酸剤、滑剤、多官能性架橋助剤、加硫促進剤等を
必要に応じて配合し、ニーダ、バンバリーミキサ、イン
タミックス、オープンロール等を用いて混練することに
よって行われる。ただし、導電性を付与させるカーボン
ブラック、カーボン繊維、金属粒子等の充填剤、抽出性
を伴う可塑剤、有機系老化防止剤あるいはイオウ系加硫
促進剤、塩素含有配合剤等の腐食を誘発させる配合剤等
の添加は行わないか、あるいはその配合量を極く少量に
とどめることが望ましい。そのため、充填剤としては、
シリカが好んで用いられる。
The preparation of a composition containing the above-mentioned components as essential components is generally carried out as a rubber compounding agent within a range that does not prevent the hardness Duro A of the obtained rubber vulcanized molded product from 20 to 50. An acid acceptor comprising a divalent metal oxide or hydroxide used, a lubricant, a multifunctional crosslinking aid, a vulcanization accelerator, etc. are blended as necessary, and a kneader, a Banbury mixer, an intermix, It is performed by kneading using an open roll or the like. However, it induces corrosion of fillers such as carbon black, carbon fiber, and metal particles that impart conductivity, a plasticizer with extractability, an organic aging inhibitor or a sulfur-based vulcanization accelerator, and a chlorine-containing compounding agent. It is desirable not to add a compounding agent or the like, or to keep the compounding amount to a very small amount. Therefore, as a filler,
Silica is preferably used.

【0011】組成物の架橋は、射出成形機、圧縮成形機
等を用いて、約150〜230℃の温度で約1〜10分間程度行
われ、必要に応じて約150〜180℃で約1〜15時間程度二
次架橋することも行われる。
The crosslinking of the composition is carried out at a temperature of about 150 to 230 ° C. for about 1 to 10 minutes by using an injection molding machine, a compression molding machine or the like, and if necessary at about 150 to 180 ° C. for about 1 to 10 minutes. Secondary crosslinking is also performed for about 15 hours.

【0012】[0012]

【発明の効果】本発明に係るゴム組成物は、低分子量分
のゴムが過酸化物架橋されるため、滲出分(抽出分)がな
くてDuro A硬度が50以下というゴムの低硬度化が達成さ
れる。このような性質を有する低硬度ゴム組成物は、二
次電池、燃料電池、アルミ電解コンデンサ、電気二重層
型コンデンサ等の電気部品に用いられる各種シール材の
成形材料として好適に用いられる。
According to the rubber composition of the present invention, since rubber having a low molecular weight is peroxide-crosslinked, there is no exudate (extractable component) and Duro A hardness of 50 or less can be reduced. Achieved. The low-hardness rubber composition having such properties is suitably used as a molding material for various sealing materials used for electric components such as secondary batteries, fuel cells, aluminum electrolytic capacitors, and electric double layer capacitors.

【0013】[0013]

【実施例】次に、実施例について本発明を説明する。Next, the present invention will be described with reference to examples.

【0014】 実施例 EPDM(三井化学製品EPT4045、Mn:105オーダー) 65重量部 エチレン・α-オレフィン共重合ゴム 35 〃 (ユニロイヤル製品トライレン65、Mn: 104オーダー) ホワイトカーボン(日本シリカ製品ニップシールLP) 15 〃 ポリメライズド (2,2,4-トリメチル-1,2-ジヒドロキノリン) 0.2 〃 ジクミルパーオキサイド 2 〃 以上の各成分をオープンロールで混練し、得られた混練
物について170℃、30分間のプレス架橋を行ない、150×
150×2mmのシート状に架橋成形した。
[0014] Example EPDM (Mitsui Chemicals product EPT4045, Mn: 10 5 order) 65 parts by weight of ethylene · alpha-olefin copolymer rubber 35 〃 (Uniroyal product Torairen 65, Mn: 10 4 order) white carbon (Nippon Silica Product Nip seal LP) 15 ポ リ Polymerized (2,2,4-trimethyl-1,2-dihydroquinoline) 0.2 〃 Dicumyl peroxide 2 〃 Each of the above components is kneaded with an open roll, and the obtained kneaded material is 170 ° C. Perform press crosslinking for 30 minutes, 150x
It was cross-linked into a 150 × 2 mm sheet.

【0015】このシート状架橋成形物について、次の各
項目の測定を行った。 硬さ(Duro A):JIS K6253準拠 引張強さ:JIS K6251準拠 伸び:JIS K6251準拠 圧縮永久歪:JIS K6262準拠(120℃、70時間) 体積固定抵抗:横河ヒューレットパッカード16008A Res
istivity Cellにより測定 アセトン抽出物:架橋ゴム5gをソックスレー抽出を行な
い、アセトン除去後の抽出物について粘稠の有無を目視
で観察
The following items were measured for the sheet-like crosslinked molded product. Hardness (Duro A): JIS K6253 compliant Tensile strength: JIS K6251 compliant Elongation: JIS K6251 compliant Compression set: JIS K6262 compliant (120 ° C, 70 hours) Volume fixed resistance: Yokogawa Hewlett Packard 16008A Res
Measured by istivity Cell Acetone extract: 5 g of crosslinked rubber is subjected to Soxhlet extraction, and the extract after acetone removal is visually observed for viscousness.

【0016】比較例1 実施例において、EPDM(EPT4045)の代りにEPDM(三井化学
製品EPT4010、Mn: 105オーダー)が100重量部用いられ、
エチレン・α-オレフィン共重合ゴムは用いられなかっ
た。
[0016] In Comparative Example 1 Example, EPDM instead of EPDM (EPT4045) (Mitsui Chemicals product EPT4010, Mn: 10 5 orders) are used 100 parts by weight,
No ethylene / α-olefin copolymer rubber was used.

【0017】比較例2 実施例において、EPDM量を20重量部に、またエチレン・
α-オレフィン共重合ゴム量を80重量部に変更した。混
練時にゴムの粘着が激しく、均一なゴムコンパウンドに
まとめることができず、成形不可であった。
Comparative Example 2 In the example, the amount of EPDM was adjusted to 20 parts by weight,
The amount of the α-olefin copolymer rubber was changed to 80 parts by weight. The rubber was strongly adhered during kneading and could not be formed into a uniform rubber compound, and molding was impossible.

【0018】比較例3 比較例1において、EPDM(EPT4010)の代りに、同量の油添
EPDM(三井化学製品EPT3041E)が用いられた。
Comparative Example 3 In Comparative Example 1, EPDM (EPT4010) was replaced with the same amount of oil-added oil.
EPDM (Mitsui Chemicals EPT3041E) was used.

【0019】以上の実施例および各比較例での測定およ
び評価結果は、次の表に示される。 表 測定・評価項目 実施例 比-1 比-3 硬さ (Duro A) 50 60 45 引張強さ (MPa) 6.6 8.9 6.7 伸び (%) 350 260 510 圧縮永久歪 (%) 11 8 15 体積固有抵抗 (MΩ・m) 2.1×1010 2.2×1010 2.1×1010 アセトン抽出物の粘稠性 なし なし あり
The results of measurement and evaluation in the above Examples and Comparative Examples are shown in the following table. Table Measurement / Evaluation items Example ratio-1 Comparison-3 Hardness (Duro A) 50 60 45 Tensile strength (MPa) 6.6 8.9 6.7 Elongation (%) 350 260 510 Compression set (%) 11 8 15 Volume resistivity (MΩ ・ m) 2.1 × 10 10 2.2 × 10 10 2.1 × 10 10 Viscosity of acetone extract No No Yes

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) H01M 2/08 H01M 2/08 X 8/02 8/02 S 8/10 8/10 Fターム(参考) 4J002 BB05X BB15W BB15X EK036 EK046 EK056 FD146 GJ02 5H011 AA17 FF01 GG02 HH02 JJ02 JJ25 JJ27 KK02 KK04 KK05 KK07 5H026 AA06 CX08 EE18 HH05 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) H01M 2/08 H01M 2/08 X 8/02 8/02 S 8/10 8/10 F term (reference) 4J002 BB05X BB15W BB15X EK036 EK046 EK056 FD146 GJ02 5H011 AA17 FF01 GG02 HH02 JJ02 JJ25 JJ27 KK02 KK04 KK05 KK07 5H026 AA06 CX08 EE18 HH05

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 数平均分子量Mnが104〜106オーダーのEP
DM約95〜30重量%および103〜105オーダーのエチレン・
α-オレフィン共重合ゴム約5〜70重量%よりなり、硬度
(Duro A)が50以下の架橋成形品を与える過酸化物架橋性
低硬度ゴム組成物。
An EP having a number average molecular weight Mn of the order of 10 4 to 10 6.
About 95 to 30% by weight of DM and about 10 3 to 10 5
α-Olefin copolymer rubber about 5-70% by weight, hardness
A peroxide-crosslinkable low-hardness rubber composition that gives a crosslinked molded article having a (Duro A) of 50 or less.
【請求項2】 電気部品シール材の成形材料として用い
られる請求項1記載の低硬度ゴム組成物。
2. The low-hardness rubber composition according to claim 1, which is used as a molding material for a sealing material for electric parts.
JP2001182751A 2001-06-18 2001-06-18 Low hardness rubber composition Withdrawn JP2002371161A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001182751A JP2002371161A (en) 2001-06-18 2001-06-18 Low hardness rubber composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001182751A JP2002371161A (en) 2001-06-18 2001-06-18 Low hardness rubber composition

Publications (2)

Publication Number Publication Date
JP2002371161A true JP2002371161A (en) 2002-12-26
JP2002371161A5 JP2002371161A5 (en) 2008-07-03

Family

ID=19022783

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001182751A Withdrawn JP2002371161A (en) 2001-06-18 2001-06-18 Low hardness rubber composition

Country Status (1)

Country Link
JP (1) JP2002371161A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004105160A1 (en) * 2003-05-22 2004-12-02 Nok Corporation Material for formation of seal for battery electrolyte
JP2008258221A (en) * 2007-03-31 2008-10-23 Nippon Chemicon Corp Electric double-layer capacitor
US8794477B2 (en) 2007-02-08 2014-08-05 Toyota Jidosha Kabushiki Kaisha Sealing material for high-pressure hydrogen container, and high-pressure hydrogen container

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004105160A1 (en) * 2003-05-22 2004-12-02 Nok Corporation Material for formation of seal for battery electrolyte
US8794477B2 (en) 2007-02-08 2014-08-05 Toyota Jidosha Kabushiki Kaisha Sealing material for high-pressure hydrogen container, and high-pressure hydrogen container
JP2008258221A (en) * 2007-03-31 2008-10-23 Nippon Chemicon Corp Electric double-layer capacitor

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