JP2000191880A - Gasket for refrigerator - Google Patents

Gasket for refrigerator

Info

Publication number
JP2000191880A
JP2000191880A JP36960498A JP36960498A JP2000191880A JP 2000191880 A JP2000191880 A JP 2000191880A JP 36960498 A JP36960498 A JP 36960498A JP 36960498 A JP36960498 A JP 36960498A JP 2000191880 A JP2000191880 A JP 2000191880A
Authority
JP
Japan
Prior art keywords
weight
conjugated diene
resin
olefin
copolymer
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
Application number
JP36960498A
Other languages
Japanese (ja)
Other versions
JP3667129B2 (en
Inventor
Keisuke Yagi
敬祐 八木
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP36960498A priority Critical patent/JP3667129B2/en
Priority to KR1019990013169A priority patent/KR19990083193A/en
Priority to TW088106152A priority patent/TWI225506B/en
Priority to MYPI99001537A priority patent/MY129280A/en
Publication of JP2000191880A publication Critical patent/JP2000191880A/en
Application granted granted Critical
Publication of JP3667129B2 publication Critical patent/JP3667129B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Refrigerator Housings (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a non-halogenated resin coping with environmental problems by using a resin composition obtained by mixing polypropylene, a hydrogenated block copolymer, a thermoplastic copolymer and a softner of a paraffin-based process oil, each mixing ratio being in a specific range. SOLUTION: 15-21 wt.% of polypropylene having MFR of 0.5-10, 25-41 wt.% of a hydrogenated block copolymer having a number average molecular weight of 100,000-200,000, the polymer block thereof comprising an aromatic vinyl compound and a conjugated diene compound as major components, the content of the aromatic vinyl compound being 5-50 wt.% and hydrogenation degree of the diene component being not less than 70%, 12-22 wt.% of a thermoplastic elastomer having xylene-insoluble content of 30-50 wt.% which is a dynamically or statically vulcanized mixture of ethylene-α.olefin(-conjugated diene) copolymer and an olefin-based resin and 26-38 wt.% of a softner having viscosity at 40 deg.C of 200-500 cSt and an aniline point of 130-160 deg.C.

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、ハロゲン等の有害
物質になる可能性が少ない樹脂を使用し環境問題に対応
した冷蔵庫ガスケットに関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a refrigerator gasket which uses a resin which is unlikely to become a harmful substance such as halogen and which is environmentally friendly.

【0002】[0002]

【従来の技術】一般に冷蔵庫ガスケットは軟質塩化ビニ
ルが使用されていたが通常冷蔵庫には食料品が貯蔵され
ており環境ホルモン等で問題になる塩化ビニル樹脂が環
境問題となっていた。また冷蔵庫の廃却時には塩化ビニ
ルの中にハロゲンを含むためダイオキシン等の問題があ
り簡単に焼却出来ない問題があった。それら問題を解決
するのに塩化ビニルを使用しない樹脂で検討を行ったが
摩耗性、コーナ部の熱溶着性が不十分、表面の粘着性が
ある等の不具合があるためにノンハロゲン樹脂の用途上
の制約が大きく、環境問題等で指摘されている塩化ビニ
ル樹脂で成形される冷蔵庫ガスケットの代替が進めない
ケースがよく発生していた。
2. Description of the Related Art In general, refrigerator gaskets are made of soft vinyl chloride, but foodstuffs are usually stored in refrigerators, and vinyl chloride resin, which is a problem with environmental hormones, has become an environmental problem. Further, when the refrigerator is disposed of, there is a problem that dioxin and the like cannot be easily incinerated because halogen is contained in vinyl chloride. In order to solve these problems, a study was conducted using a resin that does not use vinyl chloride.However, due to problems such as abrasion, insufficient heat welding at corners, and stickiness on the surface, the use of non-halogen resins was In many cases, the replacement of refrigerator gaskets made of vinyl chloride resin, which has been pointed out due to environmental issues, cannot be promoted.

【0003】[0003]

【発明が解決しようとする課題】本発明は、従来の塩化
ビニル樹脂で成形される冷蔵庫ガスケットと同じ特性を
有する環境ホルモン、ダイオキシン等の環境問題に対応
したハロゲンを含まない樹脂で成形された冷蔵庫ガスケ
ットを提供することにある。
SUMMARY OF THE INVENTION The present invention relates to a refrigerator molded from a halogen-free resin, such as environmental hormones and dioxins, having the same characteristics as conventional refrigerator gaskets molded from vinyl chloride resin. To provide a gasket.

【0004】[0004]

【課題を解決するための手段】本発明は、(a)メルト
フロ−(以下MFRと略す。:ASTM−D−1238
L条件、230℃。以下同条件)が0.5から10g/
10minのポリプロピレンを15から21重量% (b)ビニル芳香族化合物を主体とする重合体ブロック
Aの少なくとも1個以上と、共役ジエン化合物を主体と
する重合体ブロック体Bの少なくとも1個以上とを有
し、且つ、ビニル芳香族化合物の含有率が5から50重
量%の範囲にあり、共役ジエン化合物部分の70%以上
が水素添加されて、且つ、数平均分子量が10万から2
0万の水添ブロック共重合体を25から41重量% (c)動的または静的に加硫されたエチレン−α・ オ
レフィン共重合体ゴムとポリオレフィン系樹脂とのブレ
ンド体または、動的または静的に加硫されたエチレン−
α・ オレフィン−非共役ジエン共重合体ゴムとポリオ
レフィン系樹脂とのブレンド体でキシレン不溶分(溶出
条件;120℃×20時間浸せき後100メッシュで濾
過し100メッシュ残査を処理前の全体の重量で割り百
分率を求める。以下ゲル分率という)が30から50%
である熱可塑性エラストマーを12から22重量% (d)粘度(40℃)が300から500センチスト−
クスで、アニリン点が130から160℃であるパラフ
ィン系プロセスオイル軟化剤が26から38重量% よりなる樹脂を使用した冷蔵庫ガスケットである。
The present invention relates to (a) a melt flow (hereinafter abbreviated as MFR: ASTM-D-1238).
L condition, 230 ° C. Hereinafter, the same condition) is 0.5 to 10 g /
(B) at least one or more polymer blocks A mainly composed of a vinyl aromatic compound and at least one or more polymer blocks B mainly composed of a conjugated diene compound; And the content of the vinyl aromatic compound is in the range of 5 to 50% by weight, 70% or more of the conjugated diene compound is hydrogenated, and the number average molecular weight is 100,000 to 2%.
25 to 41% by weight of 100,000 hydrogenated block copolymer (c) A blend of a dynamically or statically vulcanized ethylene-α-olefin copolymer rubber and a polyolefin resin, or a dynamic or static blend Statically vulcanized ethylene
xylene-insoluble matter in a blend of α-olefin-non-conjugated diene copolymer rubber and polyolefin resin (elution condition; immersion at 120 ° C x 20 hours, filtration through 100 mesh, and 100 mesh residue as a whole before treatment) To obtain a gel percentage (hereinafter referred to as a gel fraction) of 30 to 50%.
12 to 22% by weight of a thermoplastic elastomer having a viscosity (40 ° C.) of 300 to 500 centist.
This is a refrigerator gasket using a resin containing 26 to 38% by weight of a paraffinic process oil softener having an aniline point of 130 to 160 ° C.

【0005】[0005]

【発明の実施の形態】樹脂組成中のポリプロピレンは、
得られる組成物に良好な外観、耐熱性を付与させる。ま
た、ポリプロピレンの種類としては特に規定せずホモポ
リプロピレン、ランダムポリプロピレン、ブロックポリ
プロピレンであってもよい。中でもホモポリプレピレン
が耐熱性の面で良好である。そのポリプロピレンは、M
FRが0.5から10g/10minのものでMFRが
0.5g/10min未満では組成物全体の流動性が低
くなり成形性が悪くなる。また10g/10minを越
えると水添ブロック共重合体が分散不良となり製品外観
にブツが発生したり、物性が不安定になり好ましくな
い。好ましくは、0.5から10g/10minであ
る。また添加量は15重量%未満では樹脂組成物全体の
流動性が低下し成形性が劣り、21重量%を柔軟性が損
なわれるため好ましく無い。必要に応じて上記の特性を
損なわない限り造核剤、帯電防止剤、耐候安定剤が含ま
れているポリプロピレンを使用してもよい。
DETAILED DESCRIPTION OF THE INVENTION The polypropylene in the resin composition is
Good appearance and heat resistance are imparted to the resulting composition. The type of polypropylene is not particularly limited, and may be homopolypropylene, random polypropylene, or block polypropylene. Among them, homopolypropylene is preferable in terms of heat resistance. The polypropylene is M
When the FR is 0.5 to 10 g / 10 min and the MFR is less than 0.5 g / 10 min, the flowability of the whole composition is lowered and the moldability is deteriorated. If it exceeds 10 g / 10 min, the hydrogenated block copolymer is poorly dispersed, resulting in uneven appearance of the product and unstable physical properties, which is not preferable. Preferably, it is 0.5 to 10 g / 10 min. If the addition amount is less than 15% by weight, the flowability of the entire resin composition is reduced, moldability is deteriorated, and flexibility is impaired at 21% by weight. If necessary, a polypropylene containing a nucleating agent, an antistatic agent and a weathering stabilizer may be used as long as the above properties are not impaired.

【0006】樹脂組成中の水添ブロック共重合体は、ビ
ニル芳香族化合物を主体とする重合体ブロックAの少な
くとも1個以上と、共役ジエン化合物を主体とする重合
体ブロック体Bの少なくとも1個以上とを有し、且つ、
ビニル芳香族化合物の含有率が5から50重量%の範囲
にあり、共役ジエン化合物部分の70%以上が水素添加
されて得られるものである。この水添ブロック共重合体
におけるビニル芳香族化合物としては、スチレン、α−
メチルスチレン、o,mおよびp−メチルスチレン、
1,3−ジメチルスチレン、ビニルナフタレン、ビニル
アントラセンなどがあげられる。なお、重合体Aはこれ
らの単独重合体または混合物よりなる重合体である。ま
た、共役ジエン化合物は、1,3−ブタジエン、イソプ
レン、2,3−ジメチル−1,3ブタジエン、1,3−
ペンタジエン、1,3−ヘキサジエンなどであり、重合
体ブロックBは、これらの単独重合体またはこれらの混
合物よりなる重合体である。前記水添ブロック共重合体
におけるビニル芳香族化合物の含有率は、5から50重
量%である。ビニル芳香族化合物の含有率がこの範囲を
はずれると組成物全体の剛性が高くなり柔軟性を維持で
きなくなる。
The hydrogenated block copolymer in the resin composition comprises at least one polymer block A mainly composed of a vinyl aromatic compound and at least one polymer block B mainly composed of a conjugated diene compound. Having the above, and
The content of the vinyl aromatic compound is in the range of 5 to 50% by weight, and 70% or more of the conjugated diene compound portion is obtained by hydrogenation. As the vinyl aromatic compound in the hydrogenated block copolymer, styrene, α-
Methylstyrene, o, m and p-methylstyrene,
Examples thereof include 1,3-dimethylstyrene, vinylnaphthalene, and vinylanthracene. Incidentally, the polymer A is a polymer composed of a homopolymer or a mixture thereof. The conjugated diene compounds include 1,3-butadiene, isoprene, 2,3-dimethyl-1,3 butadiene, 1,3-butadiene,
Examples thereof include pentadiene and 1,3-hexadiene, and the polymer block B is a homopolymer or a mixture of these. The content of the vinyl aromatic compound in the hydrogenated block copolymer is 5 to 50% by weight. If the content of the vinyl aromatic compound is out of this range, the rigidity of the whole composition becomes high, and the flexibility cannot be maintained.

【0007】水添ブロック共重合体の数平均分子量(M
n)は100,000以上、好ましくは、130,00
0から200,000の範囲であり、分子量分布Mw/
Mnは10以下(Mw:重量平均分子量)、好ましくは
5以下、さらに好ましくは、2以下である。数平均分子
量が100,000未満の場合、十分な耐油性を付与す
ることができない。また数平均分子量が200,000
を越えると極端に流動性が低下し成形出来なくなる。さ
らに、水添ブロック重合体は、共役ジエン部分の70%
以上が水素添加されたものである。共役ジエン部分の水
素添加率が70%未満では、極端に耐候性が劣り使用上
大きな制約ができ好ましくない。なお水添ブロック共重
合体の構造は、線状あるいは分岐状のいずれであっても
よい。また、本発明に使用される水添ブロック共重合体
は、これをさらに変性させたもの、すなわち、分子末端
または分子鎖中に水酸基、カルボキシル基、エポキシ基
等の極性基を具備するものもよい。また、ここに使用す
る水添ブロック共重合体は、数平均分子量が高いため流
動性が悪い。よって41重量%を越えると極端に流動性
悪くなりまた25重量%未満だと耐油性が損なわれれ
る。好ましくは27から33重量%である。
The number average molecular weight of the hydrogenated block copolymer (M
n) is at least 100,000, preferably 130,00
0 to 200,000, with a molecular weight distribution Mw /
Mn is 10 or less (Mw: weight average molecular weight), preferably 5 or less, more preferably 2 or less. When the number average molecular weight is less than 100,000, sufficient oil resistance cannot be provided. In addition, the number average molecular weight is 200,000
If it exceeds, the fluidity is extremely reduced and molding cannot be performed. Further, the hydrogenated block polymer has 70% of the conjugated diene portion.
The above is the result of hydrogenation. If the hydrogenation ratio of the conjugated diene portion is less than 70%, the weather resistance is extremely poor and the use is greatly restricted, which is not preferable. The structure of the hydrogenated block copolymer may be linear or branched. Further, the hydrogenated block copolymer used in the present invention may be a further modified one, that is, one having a polar group such as a hydroxyl group, a carboxyl group, or an epoxy group at the molecular terminal or in the molecular chain. . In addition, the hydrogenated block copolymer used here has a low number-average molecular weight and thus poor fluidity. Therefore, if it exceeds 41% by weight, the fluidity becomes extremely poor, and if it is less than 25% by weight, oil resistance is impaired. Preferably it is 27 to 33% by weight.

【0008】本発明で使用される動的または静的に加硫
されたエチレン−α・ オレフィン共重合体ゴムとポリ
オレフィン系樹脂とのブレンド体または、動的または静
的に加硫されたエチレン−α・ オレフィン−非共役ジ
エン共重合体ゴムとポリオレフィン系樹脂とのブレンド
体でキシレン不溶分が30から50%である熱可塑性エ
ラストマーは、熱溶着特性と成形性向上に大きく寄与
し、また外観風合いついてもハロゲン樹脂表面状態に酷
似する特徴がある。共重合体ゴムにおけるα・オレフィ
ンは、炭素数3から15のものが適する。非共役ジエン
としてはジシクロペンタジエン、1,4−ヘキサジエ
ン、エチリデンノルボルネン、及びメチレンノルボルネ
ン等が使用できる。本発明においては入手の容易さ、耐
熱特性改良の観点からα・オレフィンとしてはポリプロ
ピレンが適する。従ってゴム成分としては、いわゆるE
PDMが好適となる。共重合体ゴムのエチレン/α・オ
レフィン比は、重量比で50/50から90/10、さ
らに好ましくは、60/40から80/20が適する。
The blend of the dynamically or statically vulcanized ethylene-α-olefin copolymer rubber and the polyolefin resin used in the present invention or the dynamically or statically vulcanized ethylene- A thermoplastic elastomer having a xylene-insoluble content of 30 to 50% in a blend of an α-olefin-non-conjugated diene copolymer rubber and a polyolefin resin greatly contributes to improvement in heat welding characteristics and moldability, and appearance. Also, there is a feature very similar to the surface state of the halogen resin. As the α-olefin in the copolymer rubber, one having 3 to 15 carbon atoms is suitable. As the non-conjugated diene, dicyclopentadiene, 1,4-hexadiene, ethylidene norbornene, methylene norbornene and the like can be used. In the present invention, polypropylene is suitable as the α-olefin from the viewpoint of availability and improvement of heat resistance. Therefore, the so-called E
PDM is preferred. The ethylene / α-olefin ratio of the copolymer rubber is preferably from 50/50 to 90/10 by weight, more preferably from 60/40 to 80/20.

【0009】加硫剤としては通常のゴム用の加硫剤を用
いることができ、特に硫黄の他にアルキルフェノ−ル・
ホルムアルデヒド樹脂、ジクミルペルオキシドのような
有機過酸化物が特に好適に用いられれる。加硫剤の他に
加硫助剤、酸化防止剤等を併用してもよい。アルキルフ
ェノ−ル・ホルムアルデヒド樹脂の添加量は共重合ゴム
100重量部に対して0.5重量部から15重量部の範
囲が強度と加工性のバランスの点で好ましい。有機過酸
化物の場合、共重合ゴム100重量部に対して0.05
重量部から1重量部の範囲が強度と加工性の点で好まし
い。共重合ゴム100重量部に対して、ポリオレフィン
系樹脂を5重量部以上含むことが加工性を保つために不
可欠である。共重合体ゴムとポリオレフィン系樹脂のブ
レンド体を動的に、溶融混練させながら、加硫剤を加え
て加硫させて本成分(c)が得られる。
As the vulcanizing agent, ordinary vulcanizing agents for rubber can be used, and in particular, in addition to sulfur, alkyl phenol
Organic peroxides such as formaldehyde resin and dicumyl peroxide are particularly preferably used. In addition to the vulcanizing agent, a vulcanizing aid, an antioxidant and the like may be used in combination. The addition amount of the alkylphenol-formaldehyde resin is preferably in the range of 0.5 to 15 parts by weight based on 100 parts by weight of the copolymer rubber in view of the balance between strength and processability. In the case of an organic peroxide, 0.05 wt.
The range of 1 part by weight to 1 part by weight is preferable in view of strength and workability. It is indispensable to contain 5 parts by weight or more of the polyolefin resin with respect to 100 parts by weight of the copolymer rubber in order to maintain processability. While dynamically blending and kneading the blend of the copolymer rubber and the polyolefin resin, a vulcanizing agent is added and vulcanized to obtain the component (c).

【0010】上記の成分(c)のゲル分率(溶出条件;
キシレン中で120℃×20時間浸せき後100メッシ
ュで濾過し、100メッシュ残査を処理前の全体の重量
で割り百分率を求める。)は30重量%〜50重量%が
好ましい。ゲル分率が30重量%未満ではコーナー部の
熱溶着性が不十分であり50重量%を越えると急激に摩
耗性が低下し不具合が生じる。成分(c)の配合量は、
12から22重量%の範囲で選ぶことができる。好まし
くは、16から20重量%である。12重量%未満だと
熱溶着性が不十分でまた軟化剤で使用されるオイルによ
る表面の粘着性を押さえられなくなり成型品の外観表面
に粘着性が大きくなり好ましくない。また22重量%を
越えると極端に強度が低下し摩耗性が低下する欠点があ
る。
The gel fraction of the above component (c) (elution conditions;
After immersion in xylene at 120 ° C. for 20 hours, the mixture is filtered with 100 mesh, and the 100 mesh residue is divided by the total weight before treatment to obtain a percentage. ) Is preferably 30% by weight to 50% by weight. When the gel fraction is less than 30% by weight, the heat-welding property of the corner portion is insufficient, and when it exceeds 50% by weight, the abrasion is rapidly reduced and a problem occurs. The amount of the component (c) is
It can be selected in the range of 12 to 22% by weight. Preferably, it is 16 to 20% by weight. If the content is less than 12% by weight, the heat-sealing property is insufficient, and the adhesiveness of the surface by the oil used as the softener cannot be suppressed, and the adhesiveness on the appearance surface of the molded product is undesirably increased. On the other hand, if it exceeds 22% by weight, there is a drawback that the strength is extremely reduced and the abrasion is reduced.

【0011】樹脂組成中の軟化剤は、組成物の軟化と流
動性を付与する特性がある。軟化剤の種類としては、相
溶性の面からパラフィン系オイルが妥当でブリ−ドの点
から粘度(40℃)が300から500センチスト−ク
ス、アニリン点が130から160℃の範囲のものを使
用する必要がある。添加量は、流動性、軟化効果、ブリ
−ド、表面のベトツキの点から26から38重量%にす
る必要がある。好ましくは、30から34重量%であ
る。
The softening agent in the resin composition has characteristics of softening the composition and imparting fluidity. As a kind of the softening agent, a paraffinic oil having a viscosity (40 ° C.) of 300 to 500 centistokes and an aniline point of 130 to 160 ° C. in terms of bleed is used from the viewpoint of compatibility. There is a need to. The amount of addition should be 26 to 38% by weight from the viewpoint of fluidity, softening effect, bleed, and surface tackiness. Preferably, it is 30 to 34% by weight.

【0012】さらに必要に応じて無機充填剤、造核剤、
外滑剤、内滑剤、光安定剤、紫外線吸収剤、抗酸化剤、
着色剤、表面改質剤を添加してもよい。本発明の組成物
を製造する方法としては、通常の樹脂組成物、ゴム組成
物の製造に用いられる一般的な全ての方法を採用でき
る。基本的には、機械的溶融混練方法であり、これらに
は単軸押出機、二軸押出機、バンバリ−ミキサ−、各種
ニ−ダ−、ブラベンダ−、ロ−ル等が用いられる。ま
た、この際溶融混練する温度は180から300℃の中
から好適に選ぶことができる。ここで得られた組成物
は、熱可塑性であるので一般に使用される熱可塑性樹脂
成形機を用いて成形することが可能である。
[0012] If necessary, an inorganic filler, a nucleating agent,
Outer lubricant, inner lubricant, light stabilizer, ultraviolet absorber, antioxidant,
You may add a coloring agent and a surface modifier. As a method for producing the composition of the present invention, all general methods used for producing ordinary resin compositions and rubber compositions can be employed. Basically, it is a mechanical melt kneading method, in which a single-screw extruder, a twin-screw extruder, a Banbury mixer, various kinds of kneaders, Brabenders, rolls and the like are used. At this time, the temperature for melt-kneading can be suitably selected from 180 to 300 ° C. Since the composition obtained here is thermoplastic, it can be molded using a commonly used thermoplastic resin molding machine.

【0013】これらで得られる樹脂を通常塩化ビニルで
使用している押し出し機で成形し冷蔵庫ガスケットが成
形できる。それら押し出し成形で得られる成形物を定尺
にカットし冷蔵庫鉄板と接触する面の袋にはマグネット
を挿入しコーナー部には形状保持させるために発泡体を
少し挿入しコーナー部同志を熱溶着させ冷蔵庫ガスケッ
トを得る。
A resin gasket can be formed by molding the obtained resin with an extruder usually used for vinyl chloride. Cut the molded product obtained by extrusion molding into a fixed size, insert a magnet in the bag on the surface that comes in contact with the refrigerator iron plate, insert a little foam in the corner part to keep the shape, and heat weld the corner parts together. Obtain a refrigerator gasket.

【0014】[0014]

【実施例】以下、本発明を実施例によって更に詳細に説
明するが、本発明は、これら実施例に限定されるもので
はない。実施例及び比較例において配合した各成分は、
以下の通りである。 <成分a(1)> JPO製ポリプロピレン(MFR=
1g/10min) <成分a(2)> JPO製ポリプロピレン(MFR=
15g/10min) <成分b(1)>旭化成工業(株)製 ポリスチレン−
水素添加されたブタジエン−ポリスチレンの構造を有す
る水添ブロック共重合体(スチレン含有率:30%、水
素添加率:70%以上、数平均分子量12万) <成分b(2)>旭化成工業(株)製 ポリスチレン−
水素添加されたブタジエン−ポリスチレンの構造を有す
る水添ブロック共重合体(スチレン含有率:30%、水
素添加率:70%以上、数平均分子量6万) <成分b(3)>クラレ製 ポリスチレン−水素添加さ
れたイソプレン−ポリスチレンの構造を有する水添ブロ
ック共重合体(スチレン含有率:30%、水素添加率:
70%以上、数平均分子量17万) <成分b(4)>クラレ製 ポリスチレン−水素添加さ
れたイソプレン−ポリスチレンの構造を有する水添ブロ
ック共重合体(スチレン含有率:30%、水素添加率:
70%以上、数平均分子量8万) <成分c(1)>日本合成ゴム(株)製エチレン−プロ
ピレン共重合体(ゲル分率0%) <成分c(2)>住友化学(株)製オレフィン系熱可塑
性樹脂(ゲル分率42%)<成分d(1)>出光興産製
パラフィン系プロセスオイル(粘度(40℃)=382
センチスト−クスアニリン点=144℃) <成分d(2)>出光興産製パラフィン系プロセスオイ
ル(粘度(40℃)=96センチスト−クスアニリン点
=128℃) <成分d(3)>出光興産製ナフテン系プロセスオイル
(粘度(40℃)=238センチスト−クスアニリン点
=90℃)
EXAMPLES Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. Each component blended in Examples and Comparative Examples,
It is as follows. <Component a (1)> Polypropylene (MFR =
<1g / 10min) <Component a (2)> JPO polypropylene (MFR =
15g / 10min) <Component b (1)> Polystyrene- manufactured by Asahi Kasei Corporation
Hydrogenated block copolymer having a structure of hydrogenated butadiene-polystyrene (styrene content: 30%, hydrogenation rate: 70% or more, number average molecular weight 120,000) <Component b (2)> Asahi Kasei Corporation ) Made of polystyrene
Hydrogenated block copolymer having a hydrogenated butadiene-polystyrene structure (styrene content: 30%, hydrogenation rate: 70% or more, number average molecular weight: 60,000) <Component b (3)> Kuraray polystyrene Hydrogenated block copolymer having a hydrogenated isoprene-polystyrene structure (styrene content: 30%, hydrogenation rate:
<70% or more, number average molecular weight 170,000) <Component b (4)> Hydrogenated block copolymer having a polystyrene-hydrogenated isoprene-polystyrene structure manufactured by Kuraray (styrene content: 30%, hydrogenation rate:
70% or more, number average molecular weight 80,000) <Component c (1)> Ethylene-propylene copolymer manufactured by Nippon Synthetic Rubber Co., Ltd. (gel fraction 0%) <Component c (2)> manufactured by Sumitomo Chemical Co., Ltd. Olefin-based thermoplastic resin (gel fraction 42%) <Component d (1)> Idemitsu Kosan's paraffin-based process oil (viscosity (40 ° C) = 382)
(Centisto-kus aniline point = 144 ° C.) <Component d (2)> Idemitsu Kosan's paraffin-based process oil (viscosity (40 ° C.) = 96 centist-kus aniline point = 128 ° C.) <Component d (3)> Idemitsu Kosan's naphthenic Process oil (viscosity (40 ° C) = 238 centistokes-Kusaniline point = 90 ° C)

【0015】上記成分の(a)から(d)をバンバリ−
ミキサ−で混練温度220℃で混練しその混練物をロ−
ルに通し薄いシ−ト状にした。それを粉砕機で粉砕し角
状のペレットを作成し熱可塑性樹脂を得た。それをφ5
0mm押出し機を用いて成形し、カット、マグネット挿
入、発泡体挿入、コーナー部熱溶着行程を得て冷蔵庫ガ
スケットを得る。それから所定のテストピースを切り出
し以下に挙げる項目の評価を行った。
The above components (a) to (d) are replaced with Banbury.
Kneading with a mixer at a kneading temperature of 220 ° C.
Into a thin sheet. It was pulverized by a pulverizer to form a square pellet to obtain a thermoplastic resin. Φ5
It is molded using a 0 mm extruder, and cuts, inserts a magnet, inserts a foam, and heat-welds a corner to obtain a refrigerator gasket. Then, a predetermined test piece was cut out and the following items were evaluated.

【0016】(1)引っ張り強度:JISK6301準
拠(引っ張り速度200mm/分) 評価記号と判定基準1 ○:10Mpa以上 ×:10Mpa未満 (2)成形性と外観: φ50mm押出し機での押出し性とその表面特性の外観
を目視及び触感で評価した。 評価記号と判断基準2 ○:表面状態にベタツキが無くまた大きな異物等による
欠点もなく軟質PVCと同等に成形出来る。 ×:表面状態がベトツキがあるかまたは大きな異物欠点
があるかまたは軟質PVCと同等に成形できない。 (3)柔軟性:硬度:JIS K6301(JIS A
型、5秒後の値) 評価記号と判定基準3 ○:80未満 ×:80以上
(1) Tensile strength: JIS K6301 (tensile speed: 200 mm / min) Evaluation symbol and criteria 1 ○: 10 Mpa or more ×: less than 10 Mpa (2) Formability and appearance: Extrudability with a 50 mm extruder and its surface The appearance of the properties was evaluated visually and by touch. Evaluation symbol and criterion 2 ○: There is no stickiness in the surface state, and there is no defect due to large foreign matter and the like, and it can be molded as soft PVC. X: The surface condition is sticky, has a large foreign matter defect, or cannot be molded as well as soft PVC. (3) Flexibility: Hardness: JIS K6301 (JIS A
(Value after 5 seconds) Evaluation symbol and criterion 3 ○: less than 80 ×: 80 or more

【0017】(4)コーナー部熱溶着性 押出しで成形されたのもの同士を合わせ熱溶着機で20
0℃で約1〜2分処理後90℃ピール試験で溶着強度を
従来の塩化ビニル樹脂の溶着強度との比較で百分率で求
めた。 評価記号と判定基準4 ○:耐PVC溶着強度比率60%以上 ×:耐PVC溶着強度比率60%未満 (5)耐油性:大豆油に浸せきし40℃×48時間で放
置。その後の重量変化率を求めた 評価記号と判定基準5 ○:重量変化率10%未満 ×:重量変化率10%以上 (6)ブリ−ド特性:促進耐候試験(サンシャインウェ
ザ−、ブラックパネル温度63℃、雨有り×300hr
s)後の試験片表面状態を観察した。 評価記号と判定基準6 ○:ブリ−ド無し ×:ブリ−ド有り (7)冷蔵庫での開閉試験:冷蔵庫にガスケットを取り
付け1万回/日の割合いで20万回開閉試験を行う。 評価記号と判定基準7 ○:20万回の開閉試験で異常無し。 ×:破れ等の不具合が確認される。 これらの結果を検討結果を表1〜3に示した。
(4) Heat-welding property at the corners
After treating at 0 ° C. for about 1 to 2 minutes, the welding strength was determined by percentage in comparison with the welding strength of a conventional vinyl chloride resin in a 90 ° C. peel test. Evaluation symbol and criterion 4 :: PVC welding strength ratio of 60% or more ×: PVC welding strength ratio of less than 60% (5) Oil resistance: immersed in soybean oil and left at 40 ° C. for 48 hours. Subsequent evaluation of the weight change rate and evaluation criteria 5: Less than 10% weight change ×: More than 10% weight change (6) Bleed characteristics: Accelerated weathering test (sunshine weather, black panel temperature 63) ℃, with rain x 300hr
The surface condition of the test piece after s) was observed. Evaluation symbol and judgment criteria 6 ○: No bleed ×: With bleed (7) Opening / closing test in refrigerator: A gasket is attached to the refrigerator, and open / close test is performed 200,000 times at a rate of 10,000 times / day. Evaluation symbol and judgment standard 7 :: No abnormality in 200,000 open / close tests. ×: Defects such as tears are confirmed. These results are shown in Tables 1 to 3.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【表2】 [Table 2]

【0020】[0020]

【表3】 [Table 3]

【0021】[0021]

【発明の効果】本発明によれば、熱溶着等の2次加工が
良好で成形品の表面も艶消しでかつ柔軟でべたつきが少
なく強度、耐油性等のバランスのとれた成形加工幅の広
い外観良好なノンハロゲン熱可塑性樹脂を使用すること
で、塩化ビニルで成形される冷蔵庫ガスケットと同じ特
性をもつ環境問題に対応した冷蔵庫ガスケットが得られ
る。
According to the present invention, the secondary processing such as heat welding is good, and the surface of the molded product is matte, flexible, less sticky, and has a wide molding processing width balanced in strength, oil resistance and the like. By using a non-halogen thermoplastic resin having a good appearance, a refrigerator gasket which has the same characteristics as a refrigerator gasket formed of vinyl chloride and is compatible with environmental issues can be obtained.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(a)メルトフロ−が0.5から10g/
10minのポリプロピレンを15から21重量% (b)ビニル芳香族化合物を主体とする重合体ブロック
Aの少なくとも1個以上と、共役ジエン化合物を主体と
する重合体ブロック体Bの少なくとも1個以上とを有
し、且つ、ビニル芳香族化合物の含有率が5から50重
量%の範囲にあり、共役ジエン化合物部分の70%以上
が水素添加されて、且つ、数平均分子量が10万から2
0万の水添ブロック共重合体を25から41重量% (c)動的または静的に加硫されたエチレン−α・ オ
レフィン共重合体ゴムとポリオレフィン系樹脂とのブレ
ンド体または、動的または静的に加硫されたエチレン−
α・ オレフィン−非共役ジエン共重合体ゴムとポリオ
レフィン系樹脂とのブレンド体でキシレン不溶分が30
から50%である熱可塑性エラストマーを12から22
重量% (d)粘度(40℃)が300から500センチスト−
クスで、アニリン点が130から160℃であるパラフ
ィン系プロセスオイル軟化剤が26から38重量% よりなる樹脂を使用した冷蔵庫ガスケット。
(1) Melt flow is from 0.5 to 10 g /
(B) at least one or more polymer blocks A mainly composed of a vinyl aromatic compound and at least one or more polymer blocks B mainly composed of a conjugated diene compound; And the content of the vinyl aromatic compound is in the range of 5 to 50% by weight, 70% or more of the conjugated diene compound is hydrogenated, and the number average molecular weight is 100,000 to 2%.
25 to 41% by weight of 100,000 hydrogenated block copolymer (c) A blend of a dynamically or statically vulcanized ethylene-α-olefin copolymer rubber and a polyolefin resin, or a dynamic or static blend Statically vulcanized ethylene
α-olefin-non-conjugated diene copolymer rubber and polyolefin resin blend with 30 xylene insolubles
12 to 22% thermoplastic elastomer
% By weight (d) Viscosity (40 ° C.) of 300 to 500 centi-
A refrigerator gasket using a resin containing 26 to 38% by weight of a paraffinic process oil softener having an aniline point of 130 to 160 ° C.
JP36960498A 1998-04-27 1998-12-25 Refrigerator gasket Expired - Fee Related JP3667129B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP36960498A JP3667129B2 (en) 1998-12-25 1998-12-25 Refrigerator gasket
KR1019990013169A KR19990083193A (en) 1998-04-27 1999-04-14 Thermoplastic resin composition and refrigerator gasket
TW088106152A TWI225506B (en) 1998-04-27 1999-04-16 Thermoplastic resin composition and refrigerator gasket
MYPI99001537A MY129280A (en) 1998-04-27 1999-04-20 Refrigerator gasket

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP36960498A JP3667129B2 (en) 1998-12-25 1998-12-25 Refrigerator gasket

Publications (2)

Publication Number Publication Date
JP2000191880A true JP2000191880A (en) 2000-07-11
JP3667129B2 JP3667129B2 (en) 2005-07-06

Family

ID=18494861

Family Applications (1)

Application Number Title Priority Date Filing Date
JP36960498A Expired - Fee Related JP3667129B2 (en) 1998-04-27 1998-12-25 Refrigerator gasket

Country Status (1)

Country Link
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030096571A (en) * 2002-06-14 2003-12-31 전영식 The Profile gasket and Thermoplastics compound for Profile gasket
WO2004033974A1 (en) * 2002-10-10 2004-04-22 Young Sig Jun Profile gasket and composition thereof
JP2010085063A (en) * 2008-10-02 2010-04-15 Toshiba Corp Refrigerator

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030096571A (en) * 2002-06-14 2003-12-31 전영식 The Profile gasket and Thermoplastics compound for Profile gasket
WO2004033974A1 (en) * 2002-10-10 2004-04-22 Young Sig Jun Profile gasket and composition thereof
US7687131B2 (en) * 2002-10-10 2010-03-30 Young Sig Jun Profile gasket and composition thereof
JP2010085063A (en) * 2008-10-02 2010-04-15 Toshiba Corp Refrigerator

Also Published As

Publication number Publication date
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