JP2853952B2 - Foamable polyolefin resin composition - Google Patents
Foamable polyolefin resin compositionInfo
- Publication number
- JP2853952B2 JP2853952B2 JP5055802A JP5580293A JP2853952B2 JP 2853952 B2 JP2853952 B2 JP 2853952B2 JP 5055802 A JP5055802 A JP 5055802A JP 5580293 A JP5580293 A JP 5580293A JP 2853952 B2 JP2853952 B2 JP 2853952B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- resin
- foam
- polyolefin
- 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 - Lifetime
Links
- 229920005672 polyolefin resin Polymers 0.000 title claims description 37
- 239000011342 resin composition Substances 0.000 title claims description 7
- 229920005989 resin Polymers 0.000 claims description 19
- 239000011347 resin Substances 0.000 claims description 19
- -1 polypropylene Polymers 0.000 claims description 12
- 239000004743 Polypropylene Substances 0.000 claims description 9
- 229920001155 polypropylene Polymers 0.000 claims description 9
- 239000004711 α-olefin Substances 0.000 claims description 8
- 238000004132 cross linking Methods 0.000 claims description 7
- 239000011159 matrix material Substances 0.000 claims description 7
- 229920013716 polyethylene resin Polymers 0.000 claims description 7
- 239000000155 melt Substances 0.000 claims description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 5
- 239000004088 foaming agent Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 2
- 239000006260 foam Substances 0.000 description 33
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
- 239000005977 Ethylene Substances 0.000 description 9
- 230000005865 ionizing radiation Effects 0.000 description 9
- 230000007423 decrease Effects 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000005260 alpha ray Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- VJRITMATACIYAF-UHFFFAOYSA-N benzenesulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=CC=C1 VJRITMATACIYAF-UHFFFAOYSA-N 0.000 description 1
- 230000005250 beta ray Effects 0.000 description 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000005251 gamma ray Effects 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920005673 polypropylene based resin Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、発泡性ポリオレフィン
系樹脂組成物に関する。The present invention relates to a foamable polyolefin resin composition.
【0002】[0002]
【従来の技術】ポリオレフィン系樹脂発泡体は、柔軟
性、断熱性に優れており、従来より、天井、ドア、イン
ストルメントパネル等の車両用内装材として用いられて
きた。これらの内装材は、真空成形、圧縮成形等により
成形されるが、成形温度が高温であるため、耐熱性に優
れたポリプロピレン系樹脂を含有するポリオレフィン系
樹脂を発泡させた発泡体が主に用いられてきた。2. Description of the Related Art Polyolefin resin foams are excellent in flexibility and heat insulation, and have been used as interior materials for vehicles such as ceilings, doors and instrument panels. These interior materials are molded by vacuum molding, compression molding, etc., but since the molding temperature is high, a foam obtained by foaming a polyolefin resin containing a polypropylene resin having excellent heat resistance is mainly used. I have been.
【0003】しかしながら、ポリプロピレン系樹脂は、
架橋、発泡時に使用される電離性放射線、過酸化物等に
より分子鎖が切れて劣化し易いため、ポリプロピレン系
樹脂の他にポリエチレン系樹脂を含有するポリオレフィ
ン系樹脂を発泡させた発泡体が用いられるようになって
きた。[0003] However, polypropylene resins are
Crosslinking, ionizing radiation used at the time of foaming, the molecular chain is easily broken by peroxides and the like, so that a foam obtained by foaming a polyolefin resin containing a polyethylene resin in addition to a polypropylene resin is used. It has become.
【0004】上記ポリオレフィン系樹脂発泡体を製造す
る方法としては、例えば、特公昭46−38716号公
報及び特開昭64−87641号公報において、ポリオ
レフィン系樹脂シートを電離性放射線により架橋した
後、特定の発泡剤を用いて発泡させる方法が提案された
が、いずれも未架橋部分の劣化を防ぐことはできなかっ
た。[0004] As a method for producing the above-mentioned polyolefin resin foam, for example, Japanese Patent Publication No. 46-37716 and Japanese Patent Application Laid-Open No. 64-87641 disclose a method in which a polyolefin resin sheet is crosslinked with ionizing radiation and then crosslinked. However, none of these methods could prevent deterioration of the uncrosslinked portion.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記欠点に
鑑み、電離性放射線を照射されても劣化し難く、耐熱性
及び成形性に優れ、且つ、表皮材との接着性に優れた発
泡体を得ることのできる発泡性ポリオレフィン系樹脂組
成物を提供することを目的とする。SUMMARY OF THE INVENTION In view of the above-mentioned drawbacks, the present invention provides a foam which is hardly deteriorated even when irradiated with ionizing radiation, has excellent heat resistance and moldability, and has excellent adhesion to a skin material. An object of the present invention is to provide a foamable polyolefin-based resin composition from which a body can be obtained.
【0006】[0006]
【課題を解決するための手段】本発明において使用され
る樹脂マトリックスは、ポリプロピレン系樹脂及びポリ
エチレン系樹脂からなる樹脂マトリックスである。上記
ポリプロピレン系樹脂は、プロピレンとプロピレン以外
のα−オレフィンとを構成単位とする樹脂である。上記
プロピレン以外のα−オレフィンとしては、例えば、エ
チレン、1−ブテン、1−ペンテン、1−ヘキセン、4
−メチル−1ペンテン、1−ヘプテン、1−オクテン等
が挙げられる。Means for Solving the Problems The resin matrix used in the present invention is a resin matrix composed of a polypropylene resin and a polyethylene resin. The polypropylene resin is a resin containing propylene and an α-olefin other than propylene as constituent units. Examples of the α-olefin other than propylene include ethylene, 1-butene, 1-pentene, 1-hexene,
-Methyl-1 pentene, 1-heptene, 1-octene and the like.
【0007】上記α−オレフィンの含有量は、少なくな
っても多くなっても得られる発泡体の成形性が低下する
ため、ポリプロピレン系樹脂中2〜10重量%に限定さ
れ、好ましくは2.2〜8重量%であり、より好ましく
は2.5〜6重量%である。The content of the above-mentioned α-olefin is limited to 2 to 10% by weight in the polypropylene resin, and preferably 2.2, since the moldability of the obtained foam is reduced whether the content is low or high. -8% by weight, more preferably 2.5-6% by weight.
【0008】上記ポリプロピレン系樹脂の重量平均分子
量/数平均分子量は、小さくなると得られる発泡体の成
形性が低下し、大きくなると得られる発泡体の耐熱性が
低下するため、3〜7に限定され、好ましくは3.3〜
6.5であり、より好ましくは3.5〜6である。The weight-average molecular weight / number-average molecular weight of the above polypropylene resin is limited to 3 to 7, since the moldability of the obtained foam decreases as the molecular weight decreases and the heat resistance of the obtained foam decreases as the molecular weight increases. , Preferably 3.3 to
6.5, more preferably 3.5-6.
【0009】上記ポリプロピレン系樹脂の含有量は、少
なくなると得られる発泡体の耐熱性が低下し、多くなる
と得られる発泡体の成形性が低下するため、樹脂マトリ
ックス中40〜90重量%に限定され、好ましくは45
〜85重量%である。The content of the above polypropylene resin is limited to 40 to 90% by weight in the resin matrix because the heat resistance of the obtained foam is reduced when the content is reduced, and the moldability of the obtained foam is reduced when the content is increased. , Preferably 45
~ 85% by weight.
【0010】上記ポリエチレン系樹脂のメルトインデッ
クスは、小さくなると得られる発泡体の成形性が低下
し、大きくなると得られる発泡体の耐熱性が低下するた
め、2〜50g/10分に限定され、好ましくは3〜3
0g/10分であり、より好ましくは4〜25g/10
分である。[0010] The melt index of the polyethylene resin is limited to 2 to 50 g / 10 minutes, because the lower the melt index, the lower the moldability of the obtained foam, and the higher the melt index, the lower the heat resistance of the obtained foam. Is 3 to 3
0 g / 10 min, more preferably 4 to 25 g / 10 min.
Minutes.
【0011】上記ポリエチレン系樹脂としては、エチレ
ン単独重合体及びエチレンとエチレン以外のα−オレフ
ィンとの共重合体が挙げられ、これらが単独で用いられ
てもよいし併用されてもよい。上記エチレンの含有量
は、少なくなると得られる発泡体の成形性が低下するた
め、エチレンとエチレン以外のα−オレフィンとの共重
合体中80重量%以上であることが好ましい。Examples of the polyethylene resin include an ethylene homopolymer and a copolymer of ethylene and an α-olefin other than ethylene, and these may be used alone or in combination. The content of the ethylene is preferably 80% by weight or more in the copolymer of ethylene and an α-olefin other than ethylene, because the lower the content of ethylene, the lower the moldability of the obtained foam.
【0012】上記α−オレフィンとしては、例えば、1
−ブテン、1−ペンテン、1−ヘキセン、4−メチル−
1ペンテン、1−ヘプテン、1−オクテン等が挙げられ
る。上記ポリエチレン系樹脂の含有量は、少なくなると
得られる発泡体の成形性が低下し、多くなると得られる
発泡体の耐熱性が低下するため、樹脂マトリックス中1
0〜60重量%に限定され、好ましくは15〜55重量
%である。As the α-olefin, for example, 1
-Butene, 1-pentene, 1-hexene, 4-methyl-
1-pentene, 1-heptene, 1-octene and the like. As the content of the polyethylene resin decreases, the moldability of the obtained foam decreases, and as the content increases, the heat resistance of the obtained foam decreases.
It is limited to 0 to 60% by weight, preferably 15 to 55% by weight.
【0013】本発明において使用される架橋助剤として
は、例えば、ジビニルベンゼン、トリメチロールプロパ
ントリ(メタ)アクリレート、1,6−ヘキサンジオー
ルジ(メタ)アクリレート、1,9−ノナンジオールジ
(メタ)アクリレート、1,10−デカンジオールジ
(メタ)アクリレート、トリメリット酸トリアリルエス
テル、トリアリルイソシアヌレート、エチルビニルベン
ゼン等が挙げられ、これらが単独で用いられてもよいし
併用されてもよい。The crosslinking aid used in the present invention includes, for example, divinylbenzene, trimethylolpropane tri (meth) acrylate, 1,6-hexanediol di (meth) acrylate, and 1,9-nonanediol di (meth) acrylate. ) Acrylate, 1,10-decanediol di (meth) acrylate, triallylic acid triallyl ester, triallyl isocyanurate, ethylvinylbenzene, etc., which may be used alone or in combination .
【0014】上記架橋助剤の添加量は、少なくなっても
多くなっても得られる発泡体の成形性が低下するため、
樹脂マトリックス100重量部に対して0.5〜10重
量部に限定され、好ましくは0.8〜6重量部である。Regardless of whether the amount of the crosslinking aid is small or large, the moldability of the obtained foam is reduced.
The amount is limited to 0.5 to 10 parts by weight, preferably 0.8 to 6 parts by weight, based on 100 parts by weight of the resin matrix.
【0015】本発明において使用される熱分解型発泡剤
としては、例えば、アゾジカルボンアミド、ベンゼンス
ルホニルヒドラジド、ジニトロソペンタメチレンテトラ
ミン、トルエンスルホニルヒドラジド、4,4−オキシ
ビス(ベンゼンスルホニルヒドラジド)等が挙げられ、
これらが単独で用いられてもよいし併用されてもよい。Examples of the pyrolytic foaming agent used in the present invention include azodicarbonamide, benzenesulfonylhydrazide, dinitrosopentamethylenetetramine, toluenesulfonylhydrazide, 4,4-oxybis (benzenesulfonylhydrazide) and the like. And
These may be used alone or in combination.
【0016】上記熱分解型発泡剤の添加量は、少なくな
ると得られる発泡体の発泡性が低下し、多くなると得ら
れる発泡体の強度が低下するため、樹脂マトリックス1
00重量部に対して1〜50重量部に限定され、好まし
くは4〜25重量部である。When the amount of the above-mentioned pyrolytic foaming agent is small, the foamability of the obtained foam is reduced, and when the amount is large, the strength of the obtained foam is reduced.
The amount is limited to 1 to 50 parts by weight, preferably 4 to 25 parts by weight based on 00 parts by weight.
【0017】本発明の発泡性ポリオレフィン系樹脂組成
物の構成は上述の通りであるが、得られる発泡体の物性
を損なわない範囲内で、フェノール系、リン系、アミン
系、イオウ系等の酸化防止剤、金属害防止剤、難燃剤、
充填剤、帯電防止剤、安定剤、顔料等が添加されてもよ
い。The composition of the foamable polyolefin-based resin composition of the present invention is as described above. However, as long as the physical properties of the obtained foam are not impaired, oxidation of phenol-based, phosphorus-based, amine-based, sulfur-based, etc. Inhibitor, metal harm inhibitor, flame retardant,
Fillers, antistatic agents, stabilizers, pigments and the like may be added.
【0018】本発明の発泡性ポリオレフィン系樹脂組成
物を用いて発泡体を製造する方法としては、例えば、所
定量の樹脂マトリックス、架橋助剤及び熱分解型発泡剤
を押出機に供給し、溶融混練して押出して発泡性ポリオ
レフィン系樹脂シートを得、得られた発泡性ポリオレフ
ィン系樹脂シートに電離性放射線を所定量照射し架橋さ
せて発泡性ポリオレフィン系樹脂架橋シートを得、得ら
れた発泡性ポリオレフィン系樹脂架橋シートを発泡炉に
供給して加熱発泡させる方法が挙げられる。As a method for producing a foam using the foamable polyolefin resin composition of the present invention, for example, a predetermined amount of a resin matrix, a crosslinking assistant and a pyrolytic foaming agent are supplied to an extruder and melted. The foamed polyolefin-based resin sheet is kneaded and extruded to obtain a foamable polyolefin-based resin sheet, and the obtained foamable polyolefin-based resin sheet is irradiated with a predetermined amount of ionizing radiation and crosslinked to obtain a foamable polyolefin-based resin crosslinked sheet. A method in which a crosslinked polyolefin resin sheet is supplied to a foaming furnace and foamed by heating is used.
【0019】上記電離性放射線としては、例えば、α
線、β線、γ線等が挙げられる。上記電離性放射線の照
射量は、少なくなっても多くなっても得られる発泡体の
成形性が低下するため、1〜20Mradが好ましい。Examples of the ionizing radiation include α
Ray, β ray, γ ray and the like. The irradiation amount of the ionizing radiation is preferably 1 to 20 Mrad because the moldability of the obtained foam is reduced even if the irradiation amount is small or large.
【0020】なお、上記樹脂マトリックスを溶融混練す
るのに用いられる装置としては、例えば、単軸押出機、
2軸押出機、バンバリーミキサー、ニーダーミキサー、
ロール等が挙げられる。The apparatus used for melt-kneading the resin matrix includes, for example, a single screw extruder,
Twin screw extruder, Banbury mixer, kneader mixer,
Rolls and the like.
【0021】[0021]
【実施例】次に、本発明の実施例を説明する。なお、
「部」とあるのは「重量部」を意味する。 実施例1 (1)発泡性ポリオレフィン系樹脂シートの製造 ポリプロピレン系樹脂として、エチレン含有量が4重量
%であり、重量平均分子量/数平均分子量が4.1であ
るエチレン−プロピレン共重合体70部、ポリエチレン
系樹脂として、メルトインデックス(MI)が7g/1
0分であり、密度が0.920g/cm3 であるポリエ
チレン30部、架橋助剤としてジビニルベンゼン3部、
熱分解型発泡剤としてアゾジカルボンアミド13部、酸
化防止剤として2,6−ジ−t−ブチル−p−クレゾー
ル0.3部及びジラウリルチオプロピオネート0.3
部、金属害防止剤としてメチルベンゾトリアゾール0.
5部を単軸押出機〔池貝鉄工社製、PCM−30〕に供
給し、温度190℃で溶融混練して押し出し、厚さ1m
mの発泡性ポリオレフィン系樹脂シートを得た。Next, embodiments of the present invention will be described. In addition,
“Parts” means “parts by weight”. Example 1 (1) Production of foamable polyolefin-based resin sheet As a polypropylene-based resin, 70 parts of an ethylene-propylene copolymer having an ethylene content of 4% by weight and a weight average molecular weight / number average molecular weight of 4.1. As a polyethylene resin, the melt index (MI) is 7 g / 1.
0 minutes, 30 parts of polyethylene having a density of 0.920 g / cm 3 , 3 parts of divinylbenzene as a crosslinking aid,
13 parts of azodicarbonamide as a thermal decomposition type blowing agent, 0.3 parts of 2,6-di-t-butyl-p-cresol and 0.3 part of dilaurylthiopropionate as antioxidants
Part, methylbenzotriazole 0.
5 parts were supplied to a single screw extruder [PCM-30, manufactured by Ikegai Iron Works Co., Ltd.], melted and kneaded at a temperature of 190 ° C. and extruded to a thickness of 1 m.
m of a foamable polyolefin resin sheet was obtained.
【0022】(2)ポリオレフィン系樹脂発泡体の製造 得られた発泡性ポリオレフィン系樹脂シートに加速電圧
700KVで電離性放射線を3Mrad照射して架橋させて発
泡性ポリオレフィン系樹脂架橋シートを得、得られた発
泡性ポリオレフィン系樹脂架橋シートを縦型熱風発泡炉
に供給し、炉内温度250℃、進入速度1.7m/秒、
巻取速度6.2m/秒で連続的に延伸して加熱発泡させ
てポリオレフィン系樹脂発泡体を得た。(2) Production of polyolefin-based resin foam The obtained foamable polyolefin-based resin sheet is irradiated with 3 Mrad of ionizing radiation at an accelerating voltage of 700 KV and crosslinked to obtain a foamed polyolefin-based resin crosslinked sheet. The foamed polyolefin-based resin crosslinked sheet is supplied to a vertical hot-air foaming furnace, the furnace temperature is 250 ° C., the approach speed is 1.7 m / sec,
The film was continuously stretched at a winding speed of 6.2 m / sec and heated and foamed to obtain a polyolefin resin foam.
【0023】(3)積層体の製造 得られたポリオレフィン系樹脂発泡体の表面をコロナ放
電処理し、2液硬化型ポリエステル系接着剤〔ポリエス
テル(日立化成ポリマー社製、商品名:ハイボン)、イ
ソシアネート(住友バイエルウレタン社製、商品名:D
esmodurR)〕を用い、厚さ0.65mmの塩化
ビニル樹脂及びアクリロニトリル−ブタジエン−スチレ
ン共重合樹脂の混合樹脂シートと接着して積層体を得
た。(3) Production of Laminate The surface of the obtained polyolefin resin foam is subjected to corona discharge treatment, and a two-component curable polyester adhesive [polyester (manufactured by Hitachi Chemical Co., Ltd., trade name: Hybon), isocyanate] (Sumitomo Bayer Urethane Co., Ltd., product name: D
esmodur (R)] and bonded to a 0.65 mm-thick mixed resin sheet of a vinyl chloride resin and an acrylonitrile-butadiene-styrene copolymer resin to obtain a laminate.
【0024】実施例2〜5、比較例1〜3 表1及び2に示した所定量(部)のエチレン−プロピレ
ン共重合体、ポリエチレン及び架橋助剤を用いた以外は
実施例1と同様にして、発泡性ポリオレフィン系樹脂シ
ート、ポリオレフィン系樹脂発泡体及び積層体を得た。Examples 2 to 5 and Comparative Examples 1 to 3 The same procedures as in Example 1 were carried out except that a predetermined amount (parts) of an ethylene-propylene copolymer, polyethylene and a crosslinking aid shown in Tables 1 and 2 were used. Thus, an expandable polyolefin-based resin sheet, a polyolefin-based resin foam, and a laminate were obtained.
【0025】[0025]
【表1】 [Table 1]
【0026】[0026]
【表2】 [Table 2]
【0027】発泡性ポリオレフィン系樹脂シートの評価 上記実施例1〜5及び比較例1〜3において得られた発
泡性ポリオレフィン系樹脂シートについて、電離性放射
線が照射される前後での重量平均分子量の比を測定して
評価し、得られた結果を表3及び4に示した。なお、上
記測定は、照射量2及び4Mradそれぞれについて行っ
た。Evaluation of Expandable Polyolefin Resin Sheet The ratio of the weight average molecular weight of the expandable polyolefin resin sheets obtained in Examples 1 to 5 and Comparative Examples 1 to 3 before and after irradiation with ionizing radiation was evaluated. Was measured and evaluated, and the obtained results are shown in Tables 3 and 4. The above measurement was performed for each of the irradiation doses of 2 and 4 Mrad.
【0028】[0028]
【表3】 [Table 3]
【0029】[0029]
【表4】 [Table 4]
【0030】ポリオレフィン系樹脂発泡体の評価 上記実施例1〜5及び比較例1〜3において得られたポ
リオレフィン系樹脂発泡体について、見かけ密度 (g/
cm3)及び120℃におけるキシレン抽出残分値(重量
%)を測定し、更に、耐熱性を調べて評価し、得られた
結果を表5及び6に示した。Evaluation of Polyolefin Resin Foam The apparent density (g / g) of the polyolefin resin foams obtained in Examples 1 to 5 and Comparative Examples 1 to 3 was measured.
cm 3 ) and the residue of xylene extraction (% by weight) at 120 ° C. were measured and further evaluated by examining heat resistance. The obtained results are shown in Tables 5 and 6.
【0031】上記120℃におけるキシレン抽出残分値
は、ポリオレフィン系樹脂発泡体を0.1g採取してそ
の気泡を潰し、温度120℃のキシレン50ml中で2
4時間保持した後、200メッシュの金網を透過させた
残存物の乾燥重量(g)を量り、次式(3)により算出
した。 残分値(重量%)=(残存物の乾燥重量/0.1)×100 (3)The value of the residue of xylene extraction at 120 ° C. was determined by extracting 0.1 g of a polyolefin resin foam, crushing the bubbles, and adding 2 g in 50 ml of xylene at 120 ° C.
After holding for 4 hours, the dry weight (g) of the residue that had passed through a 200-mesh wire net was weighed and calculated by the following equation (3). Residual value (% by weight) = (dry weight of residue / 0.1) × 100 (3)
【0032】上記耐熱性は、ポリオレフィン系樹脂発泡
体を温度140℃、圧力100kg/cm2で熱圧プレスし、
該ポリオレフィン系樹脂発泡体中の気泡を観察し、気泡
が破壊しなかった場合は○、気泡が破壊した場合は×と
して示した。The above heat resistance is determined by hot pressing a polyolefin resin foam at a temperature of 140 ° C. and a pressure of 100 kg / cm 2 ,
The bubbles in the polyolefin-based resin foam were observed. When the bubbles did not break, the result was indicated by ○, and when the bubbles were broken, the result was indicated by ×.
【0033】[0033]
【表5】 [Table 5]
【0034】[0034]
【表6】 [Table 6]
【0035】積層体の評価 上記実施例1〜5及び比較例1〜3において得られた積
層体について、外観を観察して評価した後、H/D値を
測定して強度及び成形性を評価し、剥離強度を測定して
ポリオレフィン系樹脂発泡体と表皮材との接着性を評価
し、得られた結果を表7及び8に示した。上記外観は、
目視にて、膨れ、へこみ、表面荒れ等が観察されなかっ
た場合は○、1箇所でも観察された場合は×として示し
た。Evaluation of Laminate The laminate obtained in each of Examples 1 to 5 and Comparative Examples 1 to 3 was observed and evaluated for appearance, and then measured for H / D value to evaluate strength and formability. Then, the peel strength was measured to evaluate the adhesiveness between the polyolefin resin foam and the skin material, and the obtained results are shown in Tables 7 and 8. The above appearance is
When no swelling, dent, surface roughness, or the like was observed, the result was indicated by ○, and when even one portion was observed, the result was indicated by ×.
【0036】上記H/D値は、得られた積層体を遠赤外
線ヒーターで加熱してポリオレフィン系樹脂発泡体の表
層部分の温度を150〜160℃に昇温し、直径100
mmの円柱状メス型金型を用いて真空成形し、得られた
成形品の深さH(cm)及び直径D(cm)を測定して
その比H/Dを計算した。The H / D value was determined by heating the obtained laminate with a far-infrared heater to raise the temperature of the surface layer of the polyolefin resin foam to 150 to 160 ° C.
The molded product was vacuum-formed using a cylindrical female mold having a diameter of mm, the depth H (cm) and the diameter D (cm) of the obtained molded product were measured, and the ratio H / D was calculated.
【0037】上記剥離強度は、得られた積層体を切断し
て作製した幅25mm、長さ100mmの寸法の試験片
を用い、オートグラフ〔島津製作所製、DCS−500
0〕にて温度20℃又は120℃で5分間保持した後、
剥離させた際の強度(kg/25mm)をそれぞれ測定
した。The peel strength was measured using an autograph [DCS-500, manufactured by Shimadzu Corporation] using a test piece having a width of 25 mm and a length of 100 mm produced by cutting the obtained laminate.
0] at 20 ° C. or 120 ° C. for 5 minutes,
The strength (kg / 25 mm) at the time of peeling was measured.
【0038】[0038]
【表7】 [Table 7]
【0039】[0039]
【表8】 [Table 8]
【0040】[0040]
【発明の効果】本発明の発泡性ポリオレフィン系樹脂組
成物の構成は上述の通りであるから、電離性放射線を照
射されても劣化し難く、耐熱性及び成形性に優れ、且
つ、表皮材との接着性に優れたポリオレフィン系樹脂発
泡体が得られる。The composition of the foamable polyolefin resin composition of the present invention is as described above, so that it is hardly deteriorated even when irradiated with ionizing radiation, is excellent in heat resistance and moldability, and is excellent in skin material. A polyolefin-based resin foam having excellent adhesiveness can be obtained.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平4−248847(JP,A) 特開 平5−1170(JP,A) 特開 昭56−34732(JP,A) 特開 昭64−87641(JP,A) 特開 平2−102234(JP,A) 特開 平2−175227(JP,A) 特開 昭60−36535(JP,A) 特開 昭62−256842(JP,A) 特開 平3−152136(JP,A) (58)調査した分野(Int.Cl.6,DB名) C08J 9/00 - 9/42 C08L 23/04 - 23/16──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-4-248847 (JP, A) JP-A-5-1170 (JP, A) JP-A-56-34732 (JP, A) JP-A 64-64 87641 (JP, A) JP-A-2-102234 (JP, A) JP-A-2-175227 (JP, A) JP-A-60-36535 (JP, A) JP-A-62-256842 (JP, A) JP-A-3-152136 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) C08J 9/00-9/42 C08L 23/04-23/16
Claims (1)
フィンとを構成単位とし、上記α−オレフィン含有量が
2〜10重量%であり、重量平均分子量/数平均分子量
が3〜7であるポリプロピレン系樹脂40〜90重量%
と、メルトインデックスが2〜50g/10分であるポ
リエチレン系樹脂10〜60重量%とからなる樹脂マト
リックス100重量部、架橋助剤0.5〜10重量部及
び熱分解型発泡剤1〜50重量部よりなることを特徴と
する発泡性ポリオレフィン系樹脂組成物。1. A polypropylene resin comprising propylene and an α-olefin other than propylene as constituent units, wherein the α-olefin content is 2 to 10% by weight and the weight average molecular weight / number average molecular weight is 3 to 7 40-90% by weight
And 100 to 100 parts by weight of a resin matrix composed of 10 to 60% by weight of a polyethylene resin having a melt index of 2 to 50 g / 10 minutes, 0.5 to 10 parts by weight of a crosslinking aid, and 1 to 50 parts by weight of a pyrolytic foaming agent A foamable polyolefin-based resin composition comprising:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5055802A JP2853952B2 (en) | 1993-03-16 | 1993-03-16 | Foamable polyolefin resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5055802A JP2853952B2 (en) | 1993-03-16 | 1993-03-16 | Foamable polyolefin resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06263907A JPH06263907A (en) | 1994-09-20 |
JP2853952B2 true JP2853952B2 (en) | 1999-02-03 |
Family
ID=13009056
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5055802A Expired - Lifetime JP2853952B2 (en) | 1993-03-16 | 1993-03-16 | Foamable polyolefin resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2853952B2 (en) |
-
1993
- 1993-03-16 JP JP5055802A patent/JP2853952B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH06263907A (en) | 1994-09-20 |
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