JPS63312332A - Polyolefin polymer foam - Google Patents
Polyolefin polymer foamInfo
- Publication number
- JPS63312332A JPS63312332A JP14773187A JP14773187A JPS63312332A JP S63312332 A JPS63312332 A JP S63312332A JP 14773187 A JP14773187 A JP 14773187A JP 14773187 A JP14773187 A JP 14773187A JP S63312332 A JPS63312332 A JP S63312332A
- Authority
- JP
- Japan
- Prior art keywords
- foam
- polymer
- polyester
- polyolefin resin
- resin
- 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
- 239000006260 foam Substances 0.000 title claims abstract description 31
- 229920000642 polymer Polymers 0.000 title abstract description 6
- 229920000098 polyolefin Polymers 0.000 title abstract 2
- 239000000835 fiber Substances 0.000 claims abstract description 23
- 229920000728 polyester Polymers 0.000 claims abstract description 16
- 229920005672 polyolefin resin Polymers 0.000 claims description 20
- 229920001225 polyester resin Polymers 0.000 claims description 5
- 239000004645 polyester resin Substances 0.000 claims description 5
- 229920005601 base polymer Polymers 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 description 16
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- -1 polypropylene Polymers 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 238000000465 moulding Methods 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920013716 polyethylene resin Polymers 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- 239000004641 Diallyl-phthalate Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003856 thermoforming Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
【発明の詳細な説明】 (産業上の利用分野〕 本発明はポリオレフィン系樹脂発泡体に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to a polyolefin resin foam.
更に詳しく熱変形率を大幅に改善したポリオレフィン系
樹脂発泡体に関する。More specifically, the present invention relates to a polyolefin resin foam with significantly improved thermal deformation rate.
ポリオレフィン系樹脂発泡体は車輌用内装材、断熱伺な
どに多用されている。たとえば自動車等の車輌用内装材
としてはドアの内張り、天井、インストルメントパネル
などに使用されている。一方断熱材としては冷蔵庫外壁
の充填材、建物内壁の充填材、水道、カス、蒸気などの
パイプライニング材などがあげられる。Polyolefin resin foams are widely used for vehicle interior materials, insulation panels, etc. For example, they are used as interior materials for vehicles such as automobiles, such as door linings, ceilings, and instrument panels. On the other hand, examples of heat insulating materials include fillers for the outer walls of refrigerators, fillers for the inner walls of buildings, and pipe lining materials for water, waste, steam, etc.
これらの用途において、ポリオレフィン系樹脂発泡体は
独立気泡であるため、発泡倍率を適度に選択することに
より、程よい弾力性と、すぐれた断熱性が得られ、低密
度で軽いというすぐれた特性を備えてはいるが、高温に
おける熱変形率が大きいという欠点がある。In these applications, polyolefin resin foams are closed cells, so by appropriately selecting the expansion ratio, it is possible to obtain moderate elasticity and excellent heat insulation, and it has excellent properties such as low density and lightness. However, it has the disadvantage of a large thermal deformation rate at high temperatures.
したがって熱成型をする場合、高温下での成型加工性が
むずかしく、精度のよい成型品か得られないという欠点
がある。Therefore, when thermoforming is carried out, there is a drawback that molding workability at high temperatures is difficult and it is difficult to obtain molded products with high precision.
本発明は上記の目的を達成するため、次の構成からなる
ものである。In order to achieve the above object, the present invention consists of the following configuration.
すなわち、架橋型ポリオレフィン系樹脂発泡体中に裁断
されたポリエステル繊維および/またはポリエステル系
樹脂が少なくとも1重量%含有されていることを特徴と
するポリオレフィン系樹脂発泡体である。That is, it is a polyolefin resin foam characterized in that the crosslinked polyolefin resin foam contains at least 1% by weight of cut polyester fibers and/or polyester resin.
本発明を更に詳しく説明する。The present invention will be explained in more detail.
本発明に用いるポリオレフィン樹脂は低、中、高密度の
ポリエチレン樹脂は勿論、これらのポリエチレン樹脂に
おいてα−オレフィンが共重合された共重合ポリエチレ
ン樹脂、ポリプロピレン樹脂、エチレンおよび/または
ブテンが0.5〜35%ランダム、ブロック、ランダム
−ブロック状に共重合された共重合ポリプロピレン樹脂
があげられる。さらにこれらの樹脂に相溶性のあるエチ
レンを主成分とした共重合樹脂や石油樹脂を混合してな
る樹脂組成物であってもよい。The polyolefin resins used in the present invention include not only low-, medium-, and high-density polyethylene resins, but also copolymerized polyethylene resins in which α-olefin is copolymerized with these polyethylene resins, polypropylene resins, and ethylene and/or butene resins containing 0.5 to 0.5 to Examples include 35% random, block, and random-block copolymerized polypropylene resins. Furthermore, a resin composition formed by mixing a copolymer resin mainly composed of ethylene or a petroleum resin which is compatible with these resins may be used.
本発明に用いるポリオレフィン系樹脂発泡体は架橋型で
あることが好ましい。したがって架橋促進剤としてジビ
ニルベンゼン、ジアリルフタレート等を適宜の量添加す
ることができる。また発泡体の特性を損なうことのない
範囲で、着色用の顔料を始め、無機充填剤、熱安定剤、
紫外線吸収剤、酸化防止剤、造核剤などの添加剤を添加
することができる。The polyolefin resin foam used in the present invention is preferably a crosslinked type. Therefore, an appropriate amount of divinylbenzene, diallyl phthalate, etc. can be added as a crosslinking accelerator. In addition, pigments for coloring, inorganic fillers, heat stabilizers,
Additives such as ultraviolet absorbers, antioxidants, and nucleating agents can be added.
本発明に用いるポリエステル系繊維としてはボ1ノエチ
レンテレフタレートを始め、ポリエチレンテレフタレー
トにポリエチレンイソフタレートやポリブチレンテレフ
タレートを混合せしめたポリエステル繊維があげられる
。このほか共重合ポリエステル系繊維も勿論使用できる
。Examples of the polyester fiber used in the present invention include polyester fibers made of polyethylene terephthalate mixed with polyethylene isophthalate or polybutylene terephthalate. Of course, copolymerized polyester fibers can also be used.
これらの繊維は直径が2mm以下、繊維長が5mm以下
のものがよい。繊維の断面形状は問わないか、ls維に
付着している処理剤、油剤などの助剤は除去しておくこ
とが好ましい。These fibers preferably have a diameter of 2 mm or less and a fiber length of 5 mm or less. Although the cross-sectional shape of the fibers does not matter, it is preferable to remove auxiliary agents such as processing agents and oils adhering to the ls fibers.
また本発明に用いるポリエステル系樹脂は繊維と同様の
ポリマからなり、フィルムを含むシート状物を切断また
は破砕して20〜200メツシユの篩を通過するフレー
ク状のものを用いるのがよい。The polyester resin used in the present invention is made of the same polymer as fibers, and is preferably in the form of flakes that can be passed through a 20 to 200 mesh sieve by cutting or crushing a sheet-like material containing a film.
本発明において、ポリエステル繊維および/またはポリ
エステル系樹脂の含有量は、少なくとも1重量%である
ことが必要である。含有量がこれより少ないと、熱変形
率の改善効果が少ない。一方、含有量の上限は特に限定
するものではないか、その含有量は30重量%以下が好
ましい。含有量が多すぎると、発泡時、ガス扱けが生じ
ゃすくなる。In the present invention, the content of polyester fiber and/or polyester resin needs to be at least 1% by weight. If the content is less than this, the effect of improving the thermal deformation rate will be small. On the other hand, the upper limit of the content is not particularly limited, and the content is preferably 30% by weight or less. If the content is too high, it will be difficult to handle gas during foaming.
jqられた発泡体は内部にポリエステル系繊維やポリエ
ステル系フィルムのフレーク状物が分散しているため、
これらの物質が骨格となり、該発泡体を加熱、成型する
際、発泡体の熱変形を阻止するため、形態の安定した製
品とすることができる。Because the jqed foam has flakes of polyester fibers and polyester film dispersed inside it,
These substances form a skeleton and prevent the foam from being thermally deformed when the foam is heated and molded, so that a product with a stable shape can be obtained.
本発明に係るポリオレフィン系樹脂発泡体は次のような
用途に使用される。The polyolefin resin foam according to the present invention is used for the following purposes.
先ず自動車などの車輌用内装成型品のバット材が挙げら
れる。通常車輌用内装成型品は発泡体の一面に表皮材を
接合した積層体とし、更に基材と接合して内装成型品と
している。表皮材としてはポリオレフィン系樹脂シート
、ポリ塩化ビニル系樹脂シート、繊維を用いた編織物、
不織布等の布帛類があげられる。一方基材としてはAB
S樹脂シート、または成形品、ポリオレフィン系樹脂シ
ートもしくは成形品、ハードボードなどの成型品などが
あげられる。First, batt materials for molded interiors of vehicles such as automobiles are mentioned. Usually, molded interior parts for vehicles are formed into a laminate in which a skin material is bonded to one side of a foam, which is further bonded to a base material to form a molded interior part. The skin materials include polyolefin resin sheets, polyvinyl chloride resin sheets, knitted fabrics using fibers,
Examples include fabrics such as nonwoven fabrics. On the other hand, AB as a base material
Examples include S resin sheets or molded products, polyolefin resin sheets or molded products, and molded products such as hardboard.
本発明に係るポリオレフィン系樹脂発泡体の架橋方法は
電離性成eA線を用いる方法やジクミルパ一オキサイド
等の化学架橋剤を用いる化学架橋法があり、これらを単
独もしくは併用することもできる。The method for crosslinking the polyolefin resin foam according to the present invention includes a method using ionizable eA radiation and a chemical crosslinking method using a chemical crosslinking agent such as dicumyl peroxide, and these methods can be used alone or in combination.
さらに使用される発泡剤、発泡法も公知のものが使用で
きる。Furthermore, known foaming agents and foaming methods can be used.
本発明に係るポリオレフィン系樹脂発泡体は次のように
して製造することができる。The polyolefin resin foam according to the present invention can be manufactured as follows.
先ず、ポリオレフィン系樹脂(予め架橋剤、発泡剤、そ
の他の添加剤が添加されている場合は不要)に前記した
薬剤およびポリエステル系繊維もしくはフィルムのフレ
ーク状のものを混合した状態でエクストルーダに供給し
てシート状物とし、架橋、発泡処理を行うことにより得
ることができる。そして前記した積層体と基材を加熱加
圧成型もしくは加熱真空成型の手段により内装成型品と
する。First, a polyolefin resin (unnecessary if crosslinking agents, blowing agents, and other additives have been added in advance) is mixed with the above-mentioned chemicals and flakes of polyester fiber or film and fed to the extruder. It can be obtained by making a sheet-like product by crosslinking and foaming. Then, the above-described laminate and base material are formed into an interior molded product by means of heat pressure molding or heat vacuum molding.
本発明に係るポリオレフィン系樹脂発泡体を用いた前記
内装成型品は発泡体中にポリエステル系繊維やポリエス
テル系フィルムのフレーク状の骨材が分散埋設されてい
るため、これらの骨材が発泡体の熱変形を抑制すること
により、成型品の各部材間の接合部において熱変形によ
る隙間などの発生もなく、安定した形状の成型品が得ら
れる。In the interior molded product using the polyolefin resin foam according to the present invention, aggregates in the form of flakes of polyester fibers and polyester films are dispersed and embedded in the foam, so these aggregates By suppressing thermal deformation, a molded product with a stable shape can be obtained without the occurrence of gaps due to thermal deformation at the joints between the respective members of the molded product.
次に、本発明に係るポリオレフィン系樹脂発泡体は独立
気泡であり、断熱効果にすぐれており、断熱材として用
いられる。例えば、冷媒、温水の保温材としてのライニ
ング材、冷蔵庫の壁、ドアの充填材などがあげられる。Next, the polyolefin resin foam according to the present invention is a closed cell, has excellent heat insulating effect, and is used as a heat insulating material. Examples include refrigerants, lining materials for hot water insulation, and filling materials for refrigerator walls and doors.
特に、パイプやタンクなどのライニング材はその形状に
あわせて熱成型かなされるが、前)ホの如く熱変形率が
小さいので、他の樹脂からなるシートや基材との熱成型
によっても剥離しないというすぐれた特徴をもっている
。In particular, lining materials for pipes, tanks, etc. are thermoformed to suit their shape, but as shown in the previous example, their thermal deformation rate is low, so they can be easily peeled off by thermoforming with sheets or base materials made of other resins. It has the excellent feature of not
エチレンが4%共重合されたポリプロピレン樹脂80%
と、密度0.930C]/cm3、メルトインデックス
7.0のポリエチレン樹脂20%の樹脂混和物100重
量部に、熱分解型発泡剤を15重量部と架橋促進剤とし
てジアリルフタレートを5重量部配合してなる混合物に
、細かく砕断されたポリエチレンテレフタレート系ポリ
エステル繊維(100デニール、長さ1mm>を樹脂に
対して1重量部、5重量部又は10重量部均一に混合し
た組成物を、厚み2mmのシート状に成形した後、樹脂
に架橋結合を付与せしめた俊、発泡剤の分解温度以上に
加熱し発泡せしめた。80% polypropylene resin with 4% ethylene copolymerized
100 parts by weight of a 20% polyethylene resin mixture with a density of 0.930 C]/cm3 and a melt index of 7.0, 15 parts by weight of a pyrolytic blowing agent, and 5 parts by weight of diallyl phthalate as a crosslinking accelerator. A composition obtained by uniformly mixing 1, 5, or 10 parts by weight of finely chopped polyethylene terephthalate polyester fibers (100 denier, length 1 mm) with respect to the resin was added to the mixture to a thickness of 2 mm. After forming the resin into a sheet, the resin was heated to a temperature above the decomposition temperature of the foaming agent to form a cross-linked bond and foamed.
この発泡体を接着剤法によりポリプロピレン樹脂シート
と貼り合せた複合材を、加熱し真空成型法(金型直径5
0mm、深さ30mm>で成形をし、最も深いコーナ部
に於る仕上り状態(剥離、収縮性、エツジの仕上り性)
の良好なものが得られた。This foam is bonded to a polypropylene resin sheet using an adhesive method, and then the composite material is heated and vacuum formed (with a mold diameter of 5 mm).
0mm, depth 30mm>, and finish condition at the deepest corner (peeling, shrinkage, edge finish)
Good results were obtained.
一方、比較のため、ポリエステル繊維を混合しない発泡
体について、実施例と同じ成形をした結果、成形上りで
発泡体が収縮を起こし、接着界面の一部で剥離状態が観
察された。On the other hand, for comparison, a foam without polyester fiber mixed therein was molded in the same manner as in the example. As a result, the foam contracted after molding and a peeling state was observed at a part of the adhesive interface.
結果を第1表に示す。The results are shown in Table 1.
なお、ゲル分率及び接着剥離性は、次のように評価した
。In addition, the gel fraction and adhesive releasability were evaluated as follows.
(ゲル分率)
発泡体を微細に裁断し、0.10精秤し、10○メツシ
ユの金網袋に入れ、130℃の熱テトラリンで抽出する
。残量の百分率をゲル分率として表示した。(Gel fraction) The foam was cut into fine pieces, weighed to a precision of 0.10, placed in a 10○ mesh wire mesh bag, and extracted with hot tetralin at 130°C. The percentage of remaining amount was expressed as gel fraction.
(接着剥離性) ○・・・基材側に発泡体が残っている状態。(adhesive releasability) ○: Foam remains on the base material side.
△・・・部分的に基材側に発泡体が全く残っていない状
態。△: A state in which no foam remained partially on the base material side.
本発明は上記した構成とすることにより、次のようなす
ぐれた作用効果を奏するものである。By having the above-described structure, the present invention achieves the following excellent effects.
(1)発泡体となるポリオレフィン系樹脂の中に該樹脂
よりもTm (DSC>の高いポリエステル系の繊維も
しくはフィルムのフレーク状物が分散埋設されて骨材を
形成し、該骨材のためにポリエステル系樹脂発泡体の熱
変形率を抑制する結果、加熱成型法を用いても複合材を
形成する各部材間に隙間を生ずることなく剥離がないの
で、安定した製品を得ることができ、製品の品質および
収率を著しく向上させることができる。(1) Polyester fibers or film flakes with a higher Tm (DSC> than the resin) are dispersed and buried in the polyolefin resin that becomes the foam to form an aggregate. As a result of suppressing the thermal deformation rate of the polyester resin foam, even when using the heat molding method, there are no gaps between the components forming the composite material and no peeling, making it possible to obtain stable products. can significantly improve the quality and yield of
(2) 本発明に係るポリオレフィン系樹脂発泡体は
該樹脂中に前記したポリエステル系繊維やフィルムのフ
レーク状物を混合したのち溶融成型するのであるから特
殊な装置を必要とせず既存の設備で容易に製造すること
ができる。(2) Since the polyolefin resin foam according to the present invention is melt-molded after mixing the above-mentioned polyester fibers and film flakes into the resin, it does not require special equipment and can be easily used with existing equipment. can be manufactured.
Claims (1)
たポリエステル繊維および/またはポリエステル系樹脂
が少なくとも1重量%含有されていることを特徴とする
ポリオレフィン系樹脂発泡体。(1) A polyolefin resin foam characterized in that the crosslinked polyolefin resin foam contains at least 1% by weight of cut polyester fibers and/or polyester resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14773187A JPS63312332A (en) | 1987-06-12 | 1987-06-12 | Polyolefin polymer foam |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14773187A JPS63312332A (en) | 1987-06-12 | 1987-06-12 | Polyolefin polymer foam |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63312332A true JPS63312332A (en) | 1988-12-20 |
Family
ID=15436876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP14773187A Pending JPS63312332A (en) | 1987-06-12 | 1987-06-12 | Polyolefin polymer foam |
Country Status (1)
Country | Link |
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JP (1) | JPS63312332A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5426155A (en) * | 1990-10-29 | 1995-06-20 | Akzo Nobel N.V. | Anti-reversion coagents for rubber vulcanization |
WO2009119907A1 (en) * | 2008-03-27 | 2009-10-01 | 住友化学株式会社 | Foam molded product and process for producing foam molded product |
WO2009119906A1 (en) * | 2008-03-27 | 2009-10-01 | 住友化学株式会社 | Molded foam and process for producing molded foam |
-
1987
- 1987-06-12 JP JP14773187A patent/JPS63312332A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5426155A (en) * | 1990-10-29 | 1995-06-20 | Akzo Nobel N.V. | Anti-reversion coagents for rubber vulcanization |
WO2009119907A1 (en) * | 2008-03-27 | 2009-10-01 | 住友化学株式会社 | Foam molded product and process for producing foam molded product |
WO2009119906A1 (en) * | 2008-03-27 | 2009-10-01 | 住友化学株式会社 | Molded foam and process for producing molded foam |
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