JPH11263863A - Polyolefin resin foam and preparation thereof - Google Patents
Polyolefin resin foam and preparation thereofInfo
- Publication number
- JPH11263863A JPH11263863A JP10088200A JP8820098A JPH11263863A JP H11263863 A JPH11263863 A JP H11263863A JP 10088200 A JP10088200 A JP 10088200A JP 8820098 A JP8820098 A JP 8820098A JP H11263863 A JPH11263863 A JP H11263863A
- Authority
- JP
- Japan
- Prior art keywords
- fogging
- polyolefin resin
- resin foam
- odor
- polyolefin
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
- Processes Of Treating Macromolecular Substances (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)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ポリオレフィン系
樹脂発泡体およびその製造方法に関し、とくにフォギン
グテストで結晶の発生量が少なく、かつ臭気の少ないポ
リオレフィン系樹脂発泡体およびその製造方法に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyolefin resin foam and a method for producing the same, and more particularly to a polyolefin resin foam having a small amount of crystals in a fogging test and a low odor, and a method for producing the same.
【0002】[0002]
【従来の技術】ポリオレフィン系樹脂発泡体には、たと
えば車両用内装材等に用いられる場合に(たとえば、塩
化ビニルシートとともに用いられる場合に)、発泡剤の
分解によって生ずる副生物等による析出物によるくもり
(曇り)(本明細書では、以下「フォギング」と言う)
の問題がある。とくに、発泡剤としてアゾジカルボンア
ミドを用いるポリオレフィン系樹脂発泡体についても、
このような問題がある。2. Description of the Related Art Polyolefin resin foams, when used, for example, in interior materials for vehicles (for example, when used with vinyl chloride sheets), are formed by deposits such as by-products generated by decomposition of a foaming agent. Cloudy (cloudy) (hereinafter referred to as "fogging")
There is a problem. In particular, polyolefin resin foam using azodicarbonamide as a foaming agent,
There is such a problem.
【0003】また、上記フォギングの問題とともに、と
くに気温の高い、例えば夏場における車室内等において
臭気の問題がある。この臭気は、主として表皮材、例え
ば表皮材が軟質ポリ塩化ビニルシートの場合には可塑剤
と発泡体から出てくるアンモニア成分が臭気を発生させ
ると考えられる。[0003] In addition to the fogging problem, there is a problem of odor, particularly in a vehicle room or the like where the temperature is high, for example, in summer. It is considered that this odor is mainly caused by the skin material, for example, when the skin material is a soft polyvinyl chloride sheet, the plasticizer and the ammonia component coming out of the foamed body generate the odor.
【0004】このようなフォギングと臭気に関する問題
に対し、従来は、これらを一手法、たとえば一つの添加
剤にて、同時に解消するための有効な手段がなかった。Conventionally, there has been no effective means for solving such problems relating to fogging and odor by one method, for example, by one additive.
【0005】[0005]
【発明が解決しようとする課題】そこで本発明の課題
は、一つの添加剤で、フォギングテストにおいて析出物
の発生量の少なく、かつ、臭気の少ないポリオレフィン
系樹脂発泡体、およびその製造方法を提供することにあ
る。SUMMARY OF THE INVENTION An object of the present invention is to provide a polyolefin resin foam having a small amount of precipitates in a fogging test and a low odor, and a method for producing the same. Is to do.
【0006】[0006]
【課題を解決するための手段】上記課題を解決するため
に、本発明に係るポリオレフィン系樹脂発泡体は、フォ
ギング・臭気抑制剤を含有していることを特徴とするも
のからなる。このフォギング・臭気抑制剤は、1種の抑
制剤でありながらフォギングと臭気を同時に抑制できる
ものであり、代表的にはカーボンブラックを使用でき
る。In order to solve the above-mentioned problems, a polyolefin resin foam according to the present invention is characterized by containing a fogging / odor control agent. This fogging / odor suppressant can suppress fogging and odor at the same time while being a kind of suppressant. Typically, carbon black can be used.
【0007】また、本発明に係るポリオレフィン系樹脂
発泡体の製造方法は、発泡性ポリオレフィン系樹脂にフ
ォギング・臭気抑制剤を添加し、該樹脂組成物を所定形
状に成形した後発泡させることを特徴とする方法からな
る。The method for producing a polyolefin resin foam according to the present invention is characterized in that a fogging / odor control agent is added to a foamable polyolefin resin, and the resin composition is molded into a predetermined shape and then foamed. It consists of a method.
【0008】[0008]
【発明の実施の形態】以下に、本発明を、望ましい実施
の形態とともに詳細に説明する。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the present invention will be described in detail with preferred embodiments.
【0009】本発明は、ポリオレフィン系樹脂発泡体内
に、フォギング・臭気抑制剤を添加し、発泡剤の分解に
より発生する析出物の原因となる物質を抑制剤で減少さ
せることにより、フォギングテストにおいて発生する析
出物を減少させ、かつ同時に臭気の原因となる物質をも
減少させるものである。According to the present invention, a fogging / odor control agent is added to a polyolefin-based resin foam, and substances which cause precipitates generated by decomposition of the foaming agent are reduced by the inhibitor, thereby reducing the fogging test. This reduces the amount of precipitates generated, and at the same time reduces substances that cause odor.
【0010】すなわち、発泡体樹脂中にフォギング・臭
気抑制剤を含有し、フォギングテストにおいて析出物の
発生量の少なく、かつ臭気の少ないことを特徴とするポ
リオレフィン系樹脂発泡体である。[0010] That is, the present invention is a polyolefin-based resin foam which contains a fogging / odor control agent in the foam resin, generates a small amount of precipitates in a fogging test, and has a low odor.
【0011】本発明におけるオレフィン系樹脂として
は、たとえば、低密度、中〜高密度、直鎖状低密度など
のポリエチレン樹脂、エチレンと酢酸ビニルあるいは、
アクリル酸アルキルエステル、プロピレン等との共重合
体、ホモまたは共重合ポリプロピレン、塩素化ポリエチ
レン等の単独あるいは混合物を使用できる。The olefin resin in the present invention includes, for example, polyethylene resins having low density, medium to high density, linear low density, etc., ethylene and vinyl acetate, or
Alkyl acrylates, copolymers with propylene and the like, homo- or copolymerized polypropylenes, chlorinated polyethylenes and the like can be used alone or as a mixture.
【0012】本発明で使用される発泡剤としては、たと
えばアゾジカルボンアミドが使用され、その添加量は、
所望の発泡倍率により適宜調整されるが、一般的には樹
脂100重量部に対し2〜25重量部の範囲である。As the foaming agent used in the present invention, for example, azodicarbonamide is used.
Although it is appropriately adjusted depending on a desired expansion ratio, it is generally in a range of 2 to 25 parts by weight based on 100 parts by weight of the resin.
【0013】本発明で使用するフォギング・臭気抑制剤
としては、代表的にはカーボンブラックを用いる。中で
も、平均粒径が20〜150μmのカーボンブラックが
好ましく、より好ましく平均粒径が50μm以下のカー
ボンブラックである。とくに、多孔性のカーボンブラッ
クであると、吸着表面積が大きくとれるため、より好ま
しい。As the fogging / odor control agent used in the present invention, carbon black is typically used. Among them, carbon black having an average particle diameter of 20 to 150 μm is preferable, and carbon black having an average particle diameter of 50 μm or less is more preferable. In particular, porous carbon black is more preferable because the adsorption surface area can be increased.
【0014】カーボンブラックの含有量としては、ポリ
オレフィン系樹脂100重量部に対して0.05〜5重
量部の範囲が好ましく、より好ましくは0.1〜1重量
部の範囲である。The content of carbon black is preferably in the range of 0.05 to 5 parts by weight, more preferably 0.1 to 1 part by weight, based on 100 parts by weight of the polyolefin resin.
【0015】このようにフォギング・臭気抑制剤として
カーボンブラックを含有していると、フォギングの原因
となる析出物が物理的に吸着されるとともに、臭気の原
因となる尿素等も吸着され、フォギングと臭気の両方が
同時に抑制される。When carbon black is contained as a fogging / odor control agent, precipitates that cause fogging are physically adsorbed, and urea and the like that cause odors are also adsorbed. Both odors are suppressed at the same time.
【0016】本発明で使用されるフォギング・臭気抑制
剤の添加方法としては特に限定されるものではないが、
好ましくは抑制剤を含有したペレットで添加するのがよ
い。The method of adding the fogging / odor control agent used in the present invention is not particularly limited.
Preferably, it is added in the form of pellets containing an inhibitor.
【0017】発泡性樹脂組成物シートには、難燃剤、着
色剤、抗酸化剤、充填剤、発泡助剤、滑剤、架橋助剤等
を必要により適量添加することができる。To the foamable resin composition sheet, an appropriate amount of a flame retardant, a coloring agent, an antioxidant, a filler, a foaming aid, a lubricant, a crosslinking aid, and the like can be added as required.
【0018】本発明は、架橋ポリオレフィン系樹脂発泡
体にも適用でき、架橋発泡体とする場合は、一般的には
電子線による方法や、ジクミルパーオキサイド等の有機
過酸化物による化学架橋による方法が取られるが、架橋
反応性ビニルメトキシシラン等を樹脂にグラフトまたは
共重合した樹脂を用い電子線照射法や化学架橋方法も適
用できる。また、各種の架橋方法を併用して使用しても
よい。The present invention can also be applied to a crosslinked polyolefin resin foam. In the case of forming a crosslinked foam, it is generally carried out by a method using an electron beam or a chemical crosslinking using an organic peroxide such as dicumyl peroxide. Although a method can be adopted, an electron beam irradiation method or a chemical cross-linking method using a resin obtained by grafting or copolymerizing a cross-linking reactive vinylmethoxysilane or the like to the resin can also be applied. Further, various crosslinking methods may be used in combination.
【0019】架橋度は好ましくは、30〜70%が好ま
しく、より好ましくは50〜60%である。The degree of crosslinking is preferably 30 to 70%, more preferably 50 to 60%.
【0020】このような本発明に係るポリオレフィン系
樹脂発泡体は、フォギングや臭気が問題となる車両用内
装材に好適なものである。Such a polyolefin resin foam according to the present invention is suitable for a vehicular interior material in which fogging and odor are problematic.
【0021】[0021]
【実施例】以下に、本発明を実施例に基づいて説明す
る。実施におけるフォギングと臭気は、以下の方法で評
価した。 (1)フォギングテスト HAAKEのフォギング試験装置を用いて、100℃、
3時間加熱後、常温で1時間冷却した。サンプルは片面
に0.6mmの塩化ビニルのシートを接着し、塩化ビニ
ルシート面を上にしてテストを行った。析出物の有無は
50倍の顕微鏡で観察した。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below based on embodiments. Fogging and odor in the implementation were evaluated by the following methods. (1) Fogging test Using a HAAKE fogging test apparatus, 100 ° C.
After heating for 3 hours, it was cooled at room temperature for 1 hour. The sample was tested with a 0.6 mm vinyl chloride sheet adhered to one side and the vinyl chloride sheet side up. The presence or absence of the precipitate was observed under a microscope of 50 times.
【0022】(2)臭気 昭和54年度環境庁委託研究における「悪臭物質の測定
等に関する研究報告書」(日本環境衛生センター)の2
48〜250頁に記載されている、臭気強度の5点測定
法により判定した。ランク1に近づく程臭気強度は低
く、ランク5に近づく程臭気強度は高い。(2) Odor "Research Report on Measurement of Odorous Substances" commissioned by the Environment Agency in 1979 (Japan Environmental Health Center)
The odor intensity was determined by a five-point measurement method described on pages 48 to 250. The closer to rank 1, the lower the odor intensity, and the closer to rank 5, the higher the odor intensity.
【0023】実施例1〜5 プロピレンにエチレンを4重量%ランダム共重合したプ
ロピレン系樹脂(メルトインデックス2.0)80重量
部、低密度ポリエチレン(密度0.915、メルトイン
デックス8.0)20重量部に発泡剤としてアゾジカル
ボンアミド10重量部、架橋助剤としてジビニルベンゼ
ン4重量部、熱安定剤として“Irgnox”1010
を0.2重量部加え、フォギング・臭気抑制剤として平
均粒径50μmのカーボンブラックをそれぞれ0.1、
0.5、1.0、3.0、5.0重量部に調整し、ヘン
シェルミキサーで予備混合し、その混合物を90mmφ
一軸押出機(L/D=25)に投入し、発泡剤が分解し
なうよう平均樹脂温度を180℃以下に調整して混練押
出し、Tダイより押出して、それぞれ、厚み1.75m
m、幅410mmの発泡性樹脂組成物シートを5種類成
形した。Examples 1 to 5 80 parts by weight of a propylene resin (melt index 2.0) obtained by random copolymerization of propylene with 4% by weight of ethylene and 20 parts by weight of low density polyethylene (density 0.915, melt index 8.0) Parts by weight of azodicarbonamide as a foaming agent, 4 parts by weight of divinylbenzene as a crosslinking aid, and "Irgnox" 1010 as a heat stabilizer.
0.2 parts by weight of a carbon black having an average particle size of 50 μm as a fogging / odor control agent.
The mixture was adjusted to 0.5, 1.0, 3.0, and 5.0 parts by weight, and preliminarily mixed with a Henschel mixer.
The mixture was charged into a single screw extruder (L / D = 25), kneaded and extruded while adjusting the average resin temperature to 180 ° C. or lower so that the foaming agent was not decomposed, and extruded from a T-die, each having a thickness of 1.75 m.
Five types of foamable resin composition sheets having a width of 410 mm and a width of 410 mm were formed.
【0024】次に、それぞれの発泡性樹脂組成物シート
に電子線照射機(800kV)を用いて5Mradの電
子線量を照射して架橋させ、発泡性樹脂組成物架橋シー
トとした。Next, each foamable resin composition sheet was irradiated with an electron dose of 5 Mrad using an electron beam irradiator (800 kV) to crosslink, thereby obtaining a foamable resin composition crosslinked sheet.
【0025】次に、それぞれの発泡性樹脂組成物シート
を発泡装置内で、発泡剤の分解温度以上の約230〜2
40℃に加熱し、架橋発泡体を製造した。Next, each foamable resin composition sheet is placed in a foaming apparatus at a temperature of about 230 to 2 which is higher than the decomposition temperature of the foaming agent.
Heating to 40 ° C. produced a crosslinked foam.
【0026】比較例1 フォギング・臭気抑制剤を含有しない以外は上記実施例
と同様にして発泡体を製造した。Comparative Example 1 A foam was produced in the same manner as in the above example except that no fogging / odor control agent was contained.
【0027】上記6種類の発泡体について、上述のフォ
ギングテストで析出物の発生量および、臭気を調べた。
結果を表1に示す。With respect to the six types of foams, the amount of precipitates and the odor were examined by the fogging test described above.
Table 1 shows the results.
【0028】[0028]
【表1】 [Table 1]
【0029】実施例6〜8 プロピレンにエチレンを4重量%ランダム共重合したプ
ロピレン系樹脂(メルトインデックス2.0)80重量
部、低密度ポリエチレン(密度0.915、メルトイン
デックス8.0)20重量部に発泡剤としてアゾジカル
ボンアミドをそれぞれ5、10、15重量部、架橋助剤
としてジビニルベンゼン4重量部、熱安定剤として“I
rgnox”1010を0.2重量部加え、フォギング
・臭気抑制剤として平均粒径50μmのカーボンブラッ
クを5.0重量部に調整し、ヘンシェルミキサーで予備
混合し、その混合物を90mmφ一軸押出機(L/D=
25)に投入し、発泡剤が分解しないよう平均樹脂温度
を180℃以下に調整して混練押出し、Tダイより押出
して、それぞれ、厚み1.75mm、幅410mmの発
泡性樹脂組成物シートを3種類成形した。Examples 6 to 8 80 parts by weight of a propylene resin (melt index 2.0) obtained by random copolymerization of propylene with 4% by weight of ethylene and 20 parts by weight of low density polyethylene (density 0.915, melt index 8.0) 5, 10 and 15 parts by weight of azodicarbonamide as a foaming agent, 4 parts by weight of divinylbenzene as a crosslinking aid, and "I" as a heat stabilizer.
RGNOX "1010 was added in an amount of 0.2 part by weight, carbon black having an average particle diameter of 50 μm was adjusted to 5.0 parts by weight as a fogging / odor suppressant, and premixed with a Henschel mixer. The mixture was mixed with a 90 mmφ single screw extruder (L). / D =
25), kneaded and extruded while adjusting the average resin temperature to 180 ° C. or lower so that the foaming agent is not decomposed, and extruded from a T-die to obtain a foamable resin composition sheet having a thickness of 1.75 mm and a width of 410 mm. Type molded.
【0030】次に、それぞれの発泡性樹脂組成物シート
に電子線照射機(800kV)を用いて5Mradの電
子線量を照射して架橋させ、発泡性樹脂組成物架橋シー
トとした。Next, each foamable resin composition sheet was irradiated with an electron dose of 5 Mrad using an electron beam irradiator (800 kV) to crosslink, thereby obtaining a foamable resin composition crosslinked sheet.
【0031】次に、それぞれの発泡性樹脂組成物シート
を発泡装置内で、発泡剤の分解温度以上の約230〜2
40℃に加熱し、架橋発泡体を製造した。Next, each foamable resin composition sheet is placed in a foaming apparatus at a temperature of about 230 to 2 which is higher than the decomposition temperature of the foaming agent.
Heating to 40 ° C. produced a crosslinked foam.
【0032】比較例2〜4 抑制剤を含有しない以外は実施例6〜8と全く同様にし
て発泡体を製造した。Comparative Examples 2 to 4 Except that no inhibitor was contained, foams were produced in exactly the same manner as in Examples 6 to 8.
【0033】上記6種類の発泡体について、前述の方法
で析出物の有無および臭気を調べた。結果を表2に示
す。With respect to the above six types of foams, the presence of precipitates and the odor were examined by the aforementioned method. Table 2 shows the results.
【0034】[0034]
【表2】 [Table 2]
【0035】実施例9〜11 プロピレンにエチレンを4重量部ランダム共重合したプ
ロピレン系樹脂(メルトインデクス2.0)80重量
部、低密度ポリエチレン(密度0.915、メルトイン
デックス8.0)20重量部に発泡剤としてアゾジカル
ボンアミドをそれぞれ10重量部、架橋助剤としてジビ
ニルベンゼン4重量部、熱安定剤として“Irgno
x”1010を0.2重量部加え、フォギング・臭気抑
制剤として平均粒径50μmのカーボンブラックを5.
0重量部に調整し、ヘンシェルミキサーで予備混合し、
その混合物を90mmφ一軸押出機(L/D=25)に
投入し発泡剤が分解しないよう平均樹脂温度を180℃
以下に調整して混練押出し、Tダイより押出して、それ
ぞれ、厚み1.75mm、幅410mmの発泡性樹脂組
成物シートを成形した。Examples 9 to 11 4 parts by weight of propylene with ethylene 80 parts by weight of a propylene resin (melt index 2.0) obtained by random copolymerization, 20 parts by weight of low density polyethylene (density 0.915, melt index 8.0) Parts by weight of azodicarbonamide as a foaming agent, 4 parts by weight of divinylbenzene as a crosslinking aid, and "Irgno" as a heat stabilizer.
x "1010 was added in an amount of 0.2 part by weight, and carbon black having an average particle size of 50 m was used as a fogging / odor control agent.
0 parts by weight, pre-mixed with Henschel mixer,
The mixture is put into a 90 mmφ single screw extruder (L / D = 25), and the average resin temperature is set to 180 ° C. so that the foaming agent is not decomposed.
The following adjustments were made, kneaded and extruded, and extruded from a T-die to form foamable resin composition sheets each having a thickness of 1.75 mm and a width of 410 mm.
【0036】次に、それぞれの発泡性樹脂組成物シート
に電子線照射機(800kV)を用いてそれぞれ3、
5、7Mradの電子線量を照射して架橋させ、発泡性
樹脂組成物架橋シートとした。Next, each of the foamable resin composition sheets was treated with an electron beam irradiator (800 kV) to obtain 3, respectively.
The crosslinked sheet was irradiated with an electron dose of 5.7 Mrad to form a crosslinkable resin composition crosslinked sheet.
【0037】次に、それぞれの発泡性樹脂組成物シート
を発泡装置内で、発泡剤の分解温度以上の約230〜2
40℃に加熱し、架橋発泡体を製造した。Next, each foamable resin composition sheet is placed in a foaming apparatus at a temperature of about 230 to 2 which is higher than the decomposition temperature of the foaming agent.
Heating to 40 ° C. produced a crosslinked foam.
【0038】比較例5〜7 抑制剤を含有しない以外は実施例9〜11と全く同様に
して発泡体を製造した。Comparative Examples 5 to 7 Foams were produced in exactly the same manner as in Examples 9 to 11, except that no inhibitor was contained.
【0039】上記6種類の発泡体について、前述の方法
で析出物の有無および臭気を調べた。結果を表3に示
す。With respect to the above six types of foams, the presence or absence of precipitates and the odor were examined by the above-described method. Table 3 shows the results.
【0040】[0040]
【表3】 [Table 3]
【0041】表1〜表3から明らかなように、フォギン
グ・臭気抑制剤としてカーボンブラックを含有すること
により、フォギングと臭気の両方がともに良好に抑えら
れる。As is apparent from Tables 1 to 3, both fogging and odor can be suppressed well by containing carbon black as a fogging / odor suppressing agent.
【0042】[0042]
【発明の効果】本発明によれば、ポリオレフィン系樹脂
発泡体中にフォギング・臭気抑制剤を含有することによ
り、フォギングテストにおいて析出物の発生量の少な
く、かつ臭気も少ない発泡体を製造することができる。According to the present invention, a polyolefin resin foam contains a fogging / odor control agent to produce a foam having a reduced amount of precipitates and a reduced odor in a fogging test. Can be.
フロントページの続き (51)Int.Cl.6 識別記号 FI C08L 23/10 C08L 23/10 // B29C 47/14 B29C 47/14 B29K 23:00 27:00 105:04 105:24 B29L 7:00 31:58 Continued on the front page (51) Int.Cl. 6 Identification code FI C08L 23/10 C08L 23/10 // B29C 47/14 B29C 47/14 B29K 23:00 27:00 105: 04 105: 24 B29L 7:00 31:58
Claims (10)
ことを特徴とするポリオレフィン系樹脂発泡体。1. A polyolefin-based resin foam containing a fogging / odor control agent.
のカーボンブラックからなる、請求項1のポリオレフィ
ン系樹脂発泡体。2. The method according to claim 1, wherein the inhibitor has an average particle size of 20 to 150 μm.
The polyolefin-based resin foam according to claim 1, comprising carbon black.
からなる、請求項1または2のポリオレフィン系樹脂発
泡体。3. The polyolefin resin foam according to claim 1, wherein said inhibitor comprises porous carbon black.
00重量部に対し0.1〜15重量部含有されている、
請求項1ないし3のいずれかに記載のポリオレフィン系
樹脂発泡体。4. The method according to claim 1, wherein the inhibitor is a polyolefin resin.
0.1 to 15 parts by weight with respect to 00 parts by weight,
The polyolefin resin foam according to any one of claims 1 to 3.
1ないし4のいずれかに記載のポリオレフィン系樹脂発
泡体。5. The polyolefin resin foam according to claim 1, wherein the main component is polypropylene.
いずれかに記載のポリオレフィン系樹脂発泡体。6. The polyolefin resin foam according to claim 1, which is a crosslinked foam.
いし6のいずれかに記載のポリオレフィン系樹脂発泡
体。7. The polyolefin resin foam according to claim 1, which is used for an interior material for a vehicle.
グ・臭気抑制剤を添加し、該樹脂組成物を所定形状に成
形した後発泡させることを特徴とする、ポリオレフィン
系樹脂発泡体の製造方法。8. A method for producing a polyolefin-based resin foam, comprising adding a fogging / odor control agent to a foamable polyolefin-based resin, molding the resin composition into a predetermined shape, and then foaming the resin composition.
いる、請求項8のポリオレフィン系樹脂発泡体の製造方
法。9. The method for producing a polyolefin resin foam according to claim 8, wherein carbon black is used as said inhibitor.
がポリプロピレンである、請求項8または9のポリオレ
フィン系樹脂発泡体の製造方法。10. The method for producing a polyolefin resin foam according to claim 8, wherein the main component of the expandable polyolefin resin is polypropylene.
Priority Applications (1)
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JP08820098A JP3861447B2 (en) | 1998-03-17 | 1998-03-17 | Polyolefin resin foam and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP08820098A JP3861447B2 (en) | 1998-03-17 | 1998-03-17 | Polyolefin resin foam and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH11263863A true JPH11263863A (en) | 1999-09-28 |
JP3861447B2 JP3861447B2 (en) | 2006-12-20 |
Family
ID=13936266
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP08820098A Expired - Lifetime JP3861447B2 (en) | 1998-03-17 | 1998-03-17 | Polyolefin resin foam and method for producing the same |
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JP (1) | JP3861447B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102012005146A1 (en) | 2011-03-15 | 2012-09-20 | Sumitomo Chemical Co., Ltd. | Resin composition and luminaire components made therefrom |
WO2019189836A1 (en) | 2018-03-30 | 2019-10-03 | 積水化学工業株式会社 | Polyolefin resin foam, method for producing polyolefin resin foam, and molded body |
CN112752791A (en) * | 2018-09-28 | 2021-05-04 | 积水化学工业株式会社 | Crosslinked polyolefin resin foam |
-
1998
- 1998-03-17 JP JP08820098A patent/JP3861447B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102012005146A1 (en) | 2011-03-15 | 2012-09-20 | Sumitomo Chemical Co., Ltd. | Resin composition and luminaire components made therefrom |
US8895644B2 (en) | 2011-03-15 | 2014-11-25 | Sumitomo Chemical Company, Limited | Resin composition and lighting fixture components made of the same |
WO2019189836A1 (en) | 2018-03-30 | 2019-10-03 | 積水化学工業株式会社 | Polyolefin resin foam, method for producing polyolefin resin foam, and molded body |
CN112752791A (en) * | 2018-09-28 | 2021-05-04 | 积水化学工业株式会社 | Crosslinked polyolefin resin foam |
Also Published As
Publication number | Publication date |
---|---|
JP3861447B2 (en) | 2006-12-20 |
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