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JPS5829808B2 - Polyolefin resin - Google Patents

Polyolefin resin

Info

Publication number
JPS5829808B2
JPS5829808B2 JP50116320A JP11632075A JPS5829808B2 JP S5829808 B2 JPS5829808 B2 JP S5829808B2 JP 50116320 A JP50116320 A JP 50116320A JP 11632075 A JP11632075 A JP 11632075A JP S5829808 B2 JPS5829808 B2 JP S5829808B2
Authority
JP
Japan
Prior art keywords
foam
resin
weight
polyolefin resin
parts
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
Application number
JP50116320A
Other languages
Japanese (ja)
Other versions
JPS5240576A (en
Inventor
勇次 瀬尾
誠三郎 渡辺
英二 服部
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.)
Asahi Dow Ltd
Original Assignee
Asahi Dow 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 Asahi Dow Ltd filed Critical Asahi Dow Ltd
Priority to JP50116320A priority Critical patent/JPS5829808B2/en
Publication of JPS5240576A publication Critical patent/JPS5240576A/en
Publication of JPS5829808B2 publication Critical patent/JPS5829808B2/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0012Combinations of extrusion moulding with other shaping operations combined with shaping by internal pressure generated in the material, e.g. foaming
    • 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
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/022Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Molding Of Porous Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 本発明は、ポリオレフィン樹脂発泡体の押出発泡法によ
る製造方法の改良に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a method for producing a polyolefin resin foam by an extrusion foaming method.

ポリオレフィン樹脂、たとえば、低密度ポリエチレン樹
脂、高密度ポリエチレン樹脂、ポリプロピレン樹脂を押
出発泡するさいに、しばしば非常に微細な気泡を生じて
成形が困難になり、発泡体が波うったり、気泡が連続し
てしまったりする現象が生じることがあった。
When extruding and foaming polyolefin resins, such as low-density polyethylene resins, high-density polyethylene resins, and polypropylene resins, very fine bubbles are often produced, making molding difficult, resulting in wavy foam and continuous bubbles. There have been cases where the product has been damaged.

この現象の原因は不明であるが、気泡を比較的微小に制
御しようとして気泡調節剤を比較的多く使用した場合に
、特に多くあられれて、発泡体の押出成形を困難にして
いた。
The cause of this phenomenon is unknown, but when a relatively large amount of cell regulator is used in an attempt to control the bubbles to a relatively small size, a particularly large amount occurs, making extrusion molding of the foam difficult.

本発明者らは、この現象解決のため種々研究の結果、本
発明を完成したものである。
The present inventors completed the present invention as a result of various studies to solve this phenomenon.

本発明は、ポリオレフィン樹脂100重量部に対して、
1重量部以上の芳香族系石油樹脂を添加し、発泡剤を混
合して大気圧中に押出すことを特徴とするポリオレフィ
ン樹脂発泡体の製造方法である。
In the present invention, based on 100 parts by weight of polyolefin resin,
This is a method for producing a polyolefin resin foam, characterized by adding 1 part by weight or more of an aromatic petroleum resin, mixing with a blowing agent, and extruding into atmospheric pressure.

本発明に用いるポリオレフィン樹脂は、低密度ホリエチ
レン樹脂、高密度ポリエチレン樹脂、ポリプロピレン樹
脂、エチレンやプロピレンを主にし、若干の共重合成分
を含むエチレンプロピレン共重合樹脂、エチレン酢酸ビ
ニル共重合樹脂、エチレンメチルメタクリレート共重合
樹脂などを指す。
The polyolefin resins used in the present invention include low-density polyethylene resin, high-density polyethylene resin, polypropylene resin, ethylene-propylene copolymer resin containing mainly ethylene and propylene and some copolymer components, ethylene-vinyl acetate copolymer resin, ethylene-vinyl acetate copolymer resin, Refers to methyl methacrylate copolymer resin, etc.

本発明に用いる芳香族系石油樹脂とは、一般に石油樹脂
として知られる、分解ナフサ精製のさいに副生ずる低分
子量の樹脂であって、主成分は、スチレン、ビニルトル
エン、インデン等の低重合混合物であるとされている。
The aromatic petroleum resin used in the present invention is generally known as petroleum resin and is a low molecular weight resin produced as a by-product during the refining of cracked naphtha, and the main component is a low polymer mixture of styrene, vinyltoluene, indene, etc. It is said that

具体的な1例としては、商品名;ベトロジン(三井石油
化学社製)、商品名:ニスコレラ(東燃石油化学社製)
、その他数社の商品が市販され知られている。
As a specific example, product name: Vetrozin (manufactured by Mitsui Petrochemical Co., Ltd.), product name: Niscolella (manufactured by Tonen Petrochemical Co., Ltd.)
, and products from several other companies are commercially available and known.

石油樹脂を添加する量は、ポリオレフィン樹脂100重
量部に対して1重量部以上必要である。
The amount of petroleum resin added must be 1 part by weight or more per 100 parts by weight of polyolefin resin.

1重量部未満では、本発明の目的である異常発泡の防止
効果が充分でない。
If it is less than 1 part by weight, the effect of preventing abnormal foaming, which is the objective of the present invention, will not be sufficient.

添加量は1重量部以上で任意に選ぶことができ、添加量
が増すほど、異常発泡の防止効果は大きくなり、気泡径
が大きくなってくるので、気泡調節剤により気泡を調節
することが容易になる。
The amount added can be arbitrarily selected from 1 part by weight or more; the greater the amount added, the greater the effect of preventing abnormal foaming and the larger the cell diameter, making it easier to control the bubbles with a cell control agent. become.

また、石油樹脂添加の別の効果として、樹脂の流動性が
良くなってくるので、押出加工が容易になる利点がある
Another effect of adding petroleum resin is that the fluidity of the resin improves, making extrusion processing easier.

本発明において用いる発泡剤としては、プロパン、ブタ
ン、ペンタン、ヘキサンなどの炭化水素類、ジクロロジ
フロロメタン、トリクロロフロロメタン、ジクロロテト
ラフロロエタンなどのノ・ロゲン化炭化水素類、その化
ポリオレフィン樹脂の押出発泡用として知られた発泡剤
類を用いることができる。
The blowing agents used in the present invention include hydrocarbons such as propane, butane, pentane, and hexane; Foaming agents known for extrusion foaming can be used.

押出発泡体の気泡径を調節するために、各種の気泡調節
剤を使用することができる。
Various cell control agents can be used to control the cell size of the extruded foam.

また、着色剤、種々の安定剤や助剤類を用いたり、樹脂
として若干の他の樹脂類を、増量その他の目的で混合し
て使用することもできる。
Further, colorants, various stabilizers and auxiliary agents may be used, and some other resins may be mixed for the purpose of increasing the amount or for other purposes.

本発明の方法により得られるその他の効果として、発泡
体の成形後の収縮が少なくなること、および発泡体に対
する粘着剤や接着剤の接着性が改良されることが挙げら
れる。
Other benefits achieved by the method of the present invention include reduced shrinkage of the foam after molding and improved adhesion of adhesives and adhesives to the foam.

実施例 1 低密度ポリエチレン100重量部に対し、芳香族系石油
樹脂〔商品名;ベトロジン(三井石油化学社製)〕11
0重量を添加し、気泡調節剤としてメルク2重量部、滑
剤としてステアリン酸カルシウム0.5重量部を混合し
、発泡押出成形機に供給した。
Example 1 11 parts of aromatic petroleum resin [trade name: Vetrozin (manufactured by Mitsui Petrochemicals)] was added to 100 parts by weight of low-density polyethylene.
2 parts by weight of Merck as a foam regulator and 0.5 parts by weight of calcium stearate as a lubricant were mixed and the mixture was supplied to a foam extrusion molding machine.

発泡押出成形機中で、混練された樹脂に対して、樹脂1
00重量部当り20重量部のジクロロテトラフロロエタ
ンを圧入混練し、発泡押出の適温まで冷却して、管状発
泡体用の口金を通して、円管状の発泡体を押出した。
In the foaming extrusion molding machine, 1 resin is added to the kneaded resin.
20 parts by weight per 0.00 parts by weight of dichlorotetrafluoroethane were injected and kneaded, cooled to an appropriate temperature for foam extrusion, and a circular tubular foam was extruded through a die for tubular foam.

気泡径約0.4ミリの管状の良好な発泡体が得られた。A good tubular foam with a cell diameter of about 0.4 mm was obtained.

発泡体の押出直後の長さに対する、−週間経過して寸法
が安定して後の長さの減少をあられす収縮率は3%であ
った。
The shrinkage ratio of the foam to the length immediately after extrusion, which indicates a decrease in length after the dimension has stabilized after a period of -week, was 3%.

管状体の表面とアクリル系粘着剤を塗布した塩化ビニル
の粘着フィルムとの剥離強度を、速度400mm/mm
、20℃において☆☆浪1定すると、180 ?720
mmであった。
The peel strength between the surface of the tubular body and a vinyl chloride adhesive film coated with an acrylic adhesive was measured at a speed of 400 mm/mm.
, if the ☆☆ wave is constant at 20℃, it will be 180? 720
It was mm.

比較例 1 実施例1において、石油樹脂(商品名:ベトロジン)を
添加することなく、実施例1をくりかえした。
Comparative Example 1 Example 1 was repeated without adding petroleum resin (trade name: Vetrogin).

非常に微細な気泡の発泡体が得られたが、発泡体の断面
は、はg三角形に変形してしまい、円管状の発泡体の成
形は不可能であった。
Although a foam with very fine cells was obtained, the cross section of the foam was deformed into a triangular shape, making it impossible to mold the foam into a cylindrical shape.

寸法の収縮率は12%であり、表面の剥離強度は45グ
/20m7ILであった。
Dimensional shrinkage was 12% and surface peel strength was 45 g/20 m7IL.

実施例 2 高密度ポリエチレン100重量部に対し、芳香族石油樹
脂〔商品名:ニスコレラ(東燃石油化学社製)〕330
重量を添加する以外は、実施例1と同様にして、気泡径
約0.6ミリの管状の良好な発泡体を得た。
Example 2 330 parts of aromatic petroleum resin [trade name: Niscolella (manufactured by Tonen Petrochemical Co., Ltd.)] was added to 100 parts by weight of high-density polyethylene.
A good tubular foam with a cell diameter of about 0.6 mm was obtained in the same manner as in Example 1 except that the weight was added.

収縮率は8%で、剥離強度は200グ/20山であった
The shrinkage rate was 8%, and the peel strength was 200 g/20 peaks.

比較例 2 芳香族石油樹脂(商品名:ニスコレラ)を添加すること
なく、実施例2をくり返した。
Comparative Example 2 Example 2 was repeated without adding aromatic petroleum resin (trade name: Niscolella).

比較例1同様に非常に微細な気泡の発泡体を生じ、断面
ははg三角形になって、円管状の発泡体を成形できなか
った。
As in Comparative Example 1, a foam with very fine cells was produced and the cross section was triangular, making it impossible to mold a cylindrical foam.

実施例3〜5および比較例3〜4 次表の組成による以外は、実施例1と同様の操作により
発泡体を得た。
Examples 3 to 5 and Comparative Examples 3 to 4 Foams were obtained in the same manner as in Example 1 except for the compositions shown in the following table.

発泡体の収縮率、剥離強度は次表に示すとおりである。The shrinkage rate and peel strength of the foam are shown in the table below.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリオレフィン樹脂100重量部に対して、1重量
部以上の芳香族系石油樹脂を添加し、発泡剤を混合して
大気圧中に押出すことを特徴とするポリオレフィン樹脂
発泡体の製造方法。
1. A method for producing a polyolefin resin foam, which comprises adding 1 part by weight or more of an aromatic petroleum resin to 100 parts by weight of a polyolefin resin, mixing with a blowing agent, and extruding the mixture into atmospheric pressure.
JP50116320A 1975-09-29 1975-09-29 Polyolefin resin Expired JPS5829808B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50116320A JPS5829808B2 (en) 1975-09-29 1975-09-29 Polyolefin resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50116320A JPS5829808B2 (en) 1975-09-29 1975-09-29 Polyolefin resin

Publications (2)

Publication Number Publication Date
JPS5240576A JPS5240576A (en) 1977-03-29
JPS5829808B2 true JPS5829808B2 (en) 1983-06-24

Family

ID=14684055

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50116320A Expired JPS5829808B2 (en) 1975-09-29 1975-09-29 Polyolefin resin

Country Status (1)

Country Link
JP (1) JPS5829808B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5755694A (en) * 1980-09-19 1982-04-02 Matsushita Electric Ind Co Ltd Manufacture of vibration diaphragm
JPH0349873Y2 (en) * 1986-12-09 1991-10-24

Also Published As

Publication number Publication date
JPS5240576A (en) 1977-03-29

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