JPS6140345A - Polyolefin composition - Google Patents
Polyolefin compositionInfo
- Publication number
- JPS6140345A JPS6140345A JP59163329A JP16332984A JPS6140345A JP S6140345 A JPS6140345 A JP S6140345A JP 59163329 A JP59163329 A JP 59163329A JP 16332984 A JP16332984 A JP 16332984A JP S6140345 A JPS6140345 A JP S6140345A
- Authority
- JP
- Japan
- Prior art keywords
- carboxylic acid
- unsaturated carboxylic
- polyolefin
- olefin polymer
- anhydride
- 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.)
- Pending
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
■ 発明の目的
本発明は、塗装性、ホットスタンプ性などの二次加工性
に優れると共に、サーマルサイクル性およびウェルド部
の落球衝撃強度に優れるポリオレフィン組成物に関する
。DETAILED DESCRIPTION OF THE INVENTION (1) Object of the Invention The present invention relates to a polyolefin composition that is excellent in secondary processability such as paintability and hot stampability, as well as excellent thermal cycleability and drop impact strength of the weld portion.
ポリプロピレン、ポリエチレンなどのポリオレフィンは
加工性および耐衝撃性に優れ、かつ、安価であることよ
り雑貨品、自動車部品、弱電部品など多方面において用
いられている。ま丸EPDM、、SBRなどのゴム状物
質またはガラス繊維、メルク、シリカなどの無機質充填
剤を配合し耐衝撃性またはそり等の寸法安定性および剛
性を改善したポリオレフィン組成物も広く用いられてい
る。Polyolefins such as polypropylene and polyethylene have excellent processability and impact resistance, and are inexpensive, so they are used in many fields such as miscellaneous goods, automobile parts, and light electrical parts. Polyolefin compositions with improved dimensional stability and rigidity such as impact resistance or warpage are also widely used by blending rubber-like substances such as Mamaru EPDM, SBR, or inorganic fillers such as glass fiber, Merck, and silica. .
しかしながら、ポリオレフィン及びポリオレフィン組成
物は塗装、ホットスタンプなどの二次加工を行った場合
、密着力に劣り、さらに、環境温度変化に対する特性(
サーマルサイクル性)ならびにウェルド部の落球衝撃強
度に劣るといった問題点を有している。However, polyolefins and polyolefin compositions have poor adhesion when subjected to secondary processing such as painting and hot stamping, and furthermore, their properties against environmental temperature changes are poor.
It has problems such as poor thermal cycling properties) and falling ball impact strength of the weld part.
1 発明の構成
本発明者らは、従来のポリオレフィンおよびポリオレフ
ィン組成物における上述の問題点を解消すべく鋭意研究
した結果、ポリオレフィンと不飽和カルボン酸変性オレ
フィン重合体からなる組成物が、二次加工性、サーマル
サイクル性およびウェルド部の落球衝撃強度に優れるこ
とを見出し、本発明に到達したものである。1 Structure of the Invention The present inventors have conducted intensive research to solve the above-mentioned problems in conventional polyolefins and polyolefin compositions. The present invention was achieved based on the discovery that the ball has excellent properties such as thermal cycling properties, and the falling ball impact strength of the weld portion.
以下に本発明のポリオレフィン組成物について詳細に説
明する。The polyolefin composition of the present invention will be explained in detail below.
0ポリオレフイン
本発明において用いられるポリオレフィンとは、エチレ
ン、プロピレン、ブテン、インブレン、ペンテンなどを
単独または共重合して得られた重合体ならびπプロピレ
ンーエチレンブロックボリマーなどのブロックポリマー
が挙げられる。特にポリプロピレンが好ましい。0 Polyolefin Examples of the polyolefin used in the present invention include polymers obtained by singly or copolymerizing ethylene, propylene, butene, imbrene, pentene, etc., and block polymers such as π-propylene-ethylene block polymer. Particularly preferred is polypropylene.
ポリオレフィンは公知の重合法により得ることができる
。なお、構造的にみるとアイソタテイックのものとアク
クチイックのものとがあるが本発明においては伺ら制限
はなく、いずれの構造のものも利用し得る。又、同様に
分子量に関しても%に制限はない。Polyolefins can be obtained by known polymerization methods. Note that, in terms of structure, there are two types: isotatic and actuistic, but there is no restriction in the present invention, and either structure can be used. Similarly, there is no limit to the percentage of molecular weight.
0不飽和力ルボン酸変性オレフイン重合体不飽和カルボ
ン酸変性オレフィン重合体とは、不飽和カルボン酸およ
び/またはその無水物(1)とオレフィン(it) i
たは、これら(i)、(ii)と他のエチレン系不飽和
単量体(iii)からなる重合体であるO不飽和カルボ
、ン酸変性オレフィン重合体の組成比には%に制限はな
いが、不飽和カルボン酸および/またはその無水物(i
) 0.01〜20重量%、オレフィン(ii) 99
.99〜5重量%および他のエチレン系不飽和単量体Q
ii) 0〜75重量%が特に好ましい0
不飽和カルボン酸および/またはその無水物(1)とし
ては、アクリル酸、メタクリル酸等のモノカルボン酸、
マレイン酸、フマル酸、イタコン酸等のジカルボン酸、
無水マレイン酸、無水イタコン酸等のジカルボン酸無水
物等々が挙げられ、特にジカルボン酸又はその無水物が
好ましい0
オレフィンとしては、エチレン、プロピレン、ブテン−
1,4メチルペンテン−1などが挙げラレ、特にエチレ
ン、プロピレンが好ましい。0 Unsaturated carboxylic acid-modified olefin polymer The unsaturated carboxylic acid-modified olefin polymer is composed of an unsaturated carboxylic acid and/or its anhydride (1) and an olefin (it) i
Or, there is no limit to the percentage of the composition ratio of the O-unsaturated carboxylic acid-modified olefin polymer, which is a polymer composed of these (i) and (ii) and other ethylenically unsaturated monomers (iii). However, unsaturated carboxylic acids and/or their anhydrides (i
) 0.01-20% by weight, olefin (ii) 99
.. 99-5% by weight and other ethylenically unsaturated monomers Q
ii) 0 to 75% by weight is particularly preferable. Examples of the unsaturated carboxylic acid and/or its anhydride (1) include monocarboxylic acids such as acrylic acid and methacrylic acid;
dicarboxylic acids such as maleic acid, fumaric acid, itaconic acid,
Examples include dicarboxylic anhydrides such as maleic anhydride and itaconic anhydride, with dicarboxylic acids or their anhydrides being particularly preferred.Olefins include ethylene, propylene, butene-
Examples include 1,4 methylpentene-1, and ethylene and propylene are particularly preferred.
また、エチレン系不飽和化置物としては、オレフィン類
、飽和カルボン酸成分EC2〜6を含むビニルエステル
類、飽和アルコール成分にC1〜8を含むアクリル酸お
よびメタクリル酸エステル類およびマレイン酸エステル
類、ノ10ゲン化ビニル類、ビニルエーテル類、N−ビ
ニルラクタム類、カルボン酸アミド類などが挙げられる
。In addition, as ethylenically unsaturated ornaments, olefins, vinyl esters containing saturated carboxylic acid components EC2-6, acrylic acid and methacrylic acid esters and maleic esters containing C1-8 saturated alcohol components, Examples include vinyl 10-genides, vinyl ethers, N-vinyl lactams, and carboxylic acid amides.
不飽和カルボン酸変性オレフィン重合体は種々の方法で
作ることができる。例えば、オレフィン(11)または
オレフィン(11)と他のエチレン系不飽和単量体01
1〕からなる重合体に不飽和カルボン酸および/または
その無水物(1)を混合加熱する方法により得られる。Unsaturated carboxylic acid-modified olefin polymers can be made in a variety of ways. For example, olefin (11) or olefin (11) and other ethylenically unsaturated monomers 01
1] and an unsaturated carboxylic acid and/or its anhydride (1) are mixed and heated.
0ポリオレフイン組成物
本発−明のポリオレフィン組成物は、上述のポリオレフ
ィンと不飽和カルボン酸変性オレフィン重合体とからな
る0それぞれの重合体における組成比率には特に制限は
ないが、本発明の目的ならびに最終組成物の加工性の面
よりポリオレフィン99.9〜50重量%および不飽和
カルボン酸変性オレフィン重合体0.1〜50重量%で
あることが好ましい。0 Polyolefin Composition The polyolefin composition of the present invention is composed of the above-mentioned polyolefin and an unsaturated carboxylic acid-modified olefin polymer. Although there is no particular restriction on the composition ratio of each polymer, it satisfies the objectives of the present invention and From the viewpoint of processability of the final composition, it is preferable that the polyolefin content be 99.9 to 50% by weight and the unsaturated carboxylic acid-modified olefin polymer be 0.1 to 50% by weight.
さらに混合方法としては、バンバリーミキサ−1−軸押
出機、混線ブロックを有する二軸押出機等を用いた公知
の混合方法が挙げられる。Furthermore, the mixing method includes a known mixing method using a Banbury mixer, a single-screw extruder, a twin-screw extruder having a cross-wire block, and the like.
なお、ポリオレフィンと不飽和カルボン酸変性オレフィ
ン重合体とを混合する際、EPDM、SBR等のゴム状
重合体ならびにガラス繊維、メルク、シリカ、石綿、珪
酸塩、酸化チタン、黒鉛、硫化モリブデン等の充填剤を
はじめ、公知の染顔料、安定剤、可塑剤、帯電防止剤、
紫外線吸収剤、滑剤等の添加も十分可能である。In addition, when mixing the polyolefin and the unsaturated carboxylic acid-modified olefin polymer, filling with rubber-like polymers such as EPDM, SBR, glass fiber, Merck, silica, asbestos, silicate, titanium oxide, graphite, molybdenum sulfide, etc. agents, known dyes and pigments, stabilizers, plasticizers, antistatic agents,
It is also possible to add ultraviolet absorbers, lubricants, etc.
以下に実施例音用いて本発明を具体的に説明するが本発
明は、これらによって何ら制限されるものでない。The present invention will be specifically explained below using examples, but the present invention is not limited to these in any way.
〈
※1 住友化学社製”ノーブレンW −100※2 住
友化学社製“ノープレンAW−564”※3 日本ビー
ケミカル社製ウレタン系塗料” R−263″(プライ
マー゛なし)全試験片に塗布、乾燥。塗膜に縦横者10
本のカットを入れ、接着テープによる剥離試験を行い、
10/’1oo’以上の剥離を不良とした。< *1 Noprene W-100 manufactured by Sumitomo Chemical Co., Ltd. *2 “Noprene AW-564” manufactured by Sumitomo Chemical Co., Ltd. *3 Urethane paint “R-263” manufactured by Nippon Bee Chemical Co., Ltd. (without primer) applied to all test pieces, Drying.10 horizontal and vertical marks on the coating film.
A cut was made in the book and a peel test was performed using adhesive tape.
Peeling of 10/'1oo' or more was considered defective.
※4 アルミホイールを試験片上にホントスタンプ(2
00℃、3kg/crl、3秒)した後、ア徴
ルミホイー“ル上Vc従横各10本のカッ)を入れ、接
着テープによる剥離試験を行い、10/、88以上の剥
離を不良とした。*4 Real stamp the aluminum wheel on the test piece (2
00°C, 3kg/crl, 3 seconds), 10 pieces of Vc each on the upper and lower sides of the aluminum wheel were inserted, and a peel test was performed using adhesive tape. .
※5 内径30霧、高さ50謳の円筒状の金属(厚さ1
m+n ) k用いてインサート成形し、内径27.
5mm、外径33.5m+n、高さ50mの成形品を作
成した。*5 Cylindrical metal with an inner diameter of 30 mm and a height of 50 mm (thickness 1
Insert molded using m+n) k, inner diameter 27.
A molded product with a diameter of 5 mm, an outer diameter of 33.5 m+n, and a height of 50 m was created.
23℃×2時間→80℃×2時間→23℃×2時間→−
30℃×2時間→23℃×2時間を1サイクルとする試
験f:4サイクル行い試験終了後の成形品表面全観察、
ひび割れ等のるるものを不良とした。23℃ x 2 hours → 80℃ x 2 hours → 23℃ x 2 hours → -
Test f: 1 cycle of 30°C x 2 hours → 23°C x 2 hours: Perform 4 cycles and observe the entire surface of the molded product after the test,
Items with cracks, etc. were considered defective.
※6 ゲート間隔100mmの2つのゲート(各2、5
X 2. Ortan )より溶融樹脂(230℃)
を射出し、厚さ3wn縦横各150瓢の試験片を作成す
る。*6 Two gates with a gate interval of 100mm (2 and 5 gates each)
X 2. Ortan) from molten resin (230℃)
A test piece with a thickness of 3wn and 150 gourds each in the vertical and horizontal directions was prepared.
試験片を治具(高さ80rrrm、内径120yo+。Place the test piece in a jig (height 80rrrm, inner diameter 120yo+.
外径126 rrrm )の上に載せ、マイナス30℃
に調整された低温室で1#の鋼球を試験片中心部(ウェ
ルド部)K:落下させ、試験片が破壊しない最大エネル
ギー値(kg・cm )を求める。(Outer diameter: 126 rrrm) and heat at -30°C.
A 1# steel ball is dropped from the center (weld part) of the test piece in a cold room adjusted to , and the maximum energy value (kg·cm ) at which the test piece does not break is determined.
厘 発明の効果
不飽和カルボン酸変性オレフィン重合体を配合してなる
ポリオレフィン組成物は、ポリオレフィンに比べ、著し
く優れた二次加工性、サーマルサイクル性および落球衝
繋強度(ウェルド部)を有する。Effects of the Invention A polyolefin composition containing an unsaturated carboxylic acid-modified olefin polymer has significantly superior secondary processability, thermal cyclability, and falling ball impact strength (weld portion) compared to polyolefins.
Claims (1)
重合体とからなることを特徴とするポリオレフィン組成
物。 2)ポリオレフィンが99.9〜50重量%、不飽和カ
ルボン酸変性オレフィン重合体が0.1〜50重量%で
ある特許請求の範囲第1項記載のポリオレフィン組成物
。[Scope of Claims] 1) A polyolefin composition comprising a polyolefin and an unsaturated carboxylic acid-modified olefin polymer. 2) The polyolefin composition according to claim 1, wherein the polyolefin is 99.9 to 50% by weight and the unsaturated carboxylic acid-modified olefin polymer is 0.1 to 50% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59163329A JPS6140345A (en) | 1984-08-01 | 1984-08-01 | Polyolefin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59163329A JPS6140345A (en) | 1984-08-01 | 1984-08-01 | Polyolefin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6140345A true JPS6140345A (en) | 1986-02-26 |
Family
ID=15771781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59163329A Pending JPS6140345A (en) | 1984-08-01 | 1984-08-01 | Polyolefin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6140345A (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57182340A (en) * | 1981-05-07 | 1982-11-10 | Asahi Chem Ind Co Ltd | Polyethylene composition |
| JPS60124645A (en) * | 1983-12-09 | 1985-07-03 | Mitsubishi Petrochem Co Ltd | Glass fiber reinforced resin composition |
| JPS60248741A (en) * | 1984-05-23 | 1985-12-09 | Achilles Corp | Polyolefin molded article |
-
1984
- 1984-08-01 JP JP59163329A patent/JPS6140345A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57182340A (en) * | 1981-05-07 | 1982-11-10 | Asahi Chem Ind Co Ltd | Polyethylene composition |
| JPS60124645A (en) * | 1983-12-09 | 1985-07-03 | Mitsubishi Petrochem Co Ltd | Glass fiber reinforced resin composition |
| JPS60248741A (en) * | 1984-05-23 | 1985-12-09 | Achilles Corp | Polyolefin molded article |
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