JPH04272939A - Foamable resin composition - Google Patents

Foamable resin composition

Info

Publication number
JPH04272939A
JPH04272939A JP3033143A JP3314391A JPH04272939A JP H04272939 A JPH04272939 A JP H04272939A JP 3033143 A JP3033143 A JP 3033143A JP 3314391 A JP3314391 A JP 3314391A JP H04272939 A JPH04272939 A JP H04272939A
Authority
JP
Japan
Prior art keywords
weight
resin
foaming
combustion ash
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.)
Granted
Application number
JP3033143A
Other languages
Japanese (ja)
Other versions
JP2589222B2 (en
Inventor
Motohiro Kondo
元博 近藤
Takamune Suzuki
隆領 鈴木
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.)
Toyota Motor Corp
Kojima Industries Corp
Original Assignee
Kojima Press Industry Co Ltd
Toyota Motor Corp
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 Kojima Press Industry Co Ltd, Toyota Motor Corp filed Critical Kojima Press Industry Co Ltd
Priority to JP3033143A priority Critical patent/JP2589222B2/en
Publication of JPH04272939A publication Critical patent/JPH04272939A/en
Application granted granted Critical
Publication of JP2589222B2 publication Critical patent/JP2589222B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To prepare the title compsn. which gives a light-wt. molded article having a fine and homogeneous cell structure without detriment to the physical properties. CONSTITUTION:The title compsn. comprises 100 pts.wt. thermoplastic resin contg. 40wt.% or lower ash having a specific surface area of 9X10<3>cm<2>/g or higher and 0.05-1.0 pt.wt. chemical blowing agent, and can be molded into a foamed article having a high foaming ratio and a high bending modulus.

Description

【発明の詳細な説明】[Detailed description of the invention]

【0001】0001

【産業上の利用分野】本発明は、発泡成形体を成形する
のに使用される発泡用樹脂組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a foaming resin composition used for molding foamed articles.

【0002】0002

【従来の技術】従来、発泡用樹脂組成物は、軽量化、低
コスト化が可能なため汎用的に使用されており、射出成
形用の発泡剤も各種上市され各種の熱可塑性樹脂に添加
して発泡成形が可能である。ところで、発泡用樹脂組成
物を高温で射出成形すると、発泡はしやすくなるが熱の
影響が大きくなり、成形品の物性の低下、外観不良がお
きやすくまた最大の問題点は歪みやそりが大きくなる。 このため低温で発泡成形できる樹脂組成物が求められて
いる。そのために化学発泡剤を使用して発泡させる組成
物が知られている。たとえば、特開平2−120334
号公報には射出成形用軟質発泡樹脂組成物として熱可塑
性ブロック共重合体40〜70重量%、ポリオレフィン
系樹脂10〜40重量%、ゴム用軟化剤5〜25重量%
とからなる樹脂組成物に、化学発泡剤を前記の組成物の
合計100重量部に対して0.2〜3重量部配合した組
成物が開示されている。
[Prior Art] Conventionally, foaming resin compositions have been widely used because they can be lightweight and cost-reduced, and various foaming agents for injection molding have been commercially available and are added to various thermoplastic resins. Foam molding is possible. By the way, when foaming resin compositions are injection molded at high temperatures, foaming becomes easier, but the effects of heat are greater, resulting in a decline in the physical properties of the molded product and poor appearance, and the biggest problem is that it causes large distortions and warpage. Become. Therefore, there is a need for a resin composition that can be foam-molded at low temperatures. For this purpose, compositions that are foamed using chemical foaming agents are known. For example, JP-A-2-120334
The publication describes a soft foam resin composition for injection molding containing 40 to 70% by weight of a thermoplastic block copolymer, 10 to 40% by weight of a polyolefin resin, and 5 to 25% by weight of a rubber softener.
A composition is disclosed in which 0.2 to 3 parts by weight of a chemical blowing agent is added to a resin composition consisting of the following, based on a total of 100 parts by weight of the above composition.

【0003】しかしこれらの発泡成形用樹脂組成物は、
成形性、外観、柔軟性の改良の提案はあるが、機械的強
度の低下の改善については殆ど提案されていない。発泡
成形品では、発泡状態を均一とするために気泡がミクロ
で均一に分散していることが必要である。特に気泡が大
きいとそこに応力集中が起こり、ミクロクレーズが発生
し物性の低下をきたす。このことは樹脂に粒子状の充填
剤を分散させた場合と同様で、分散粒子界面に応力が集
中するのと同じであると推定される。このため、発泡成
形品では発泡率を高くして軽量化すると成形品の剛性が
低下する傾向にある。したがって、発泡成形品は自動車
部品、電気部品などの構造部品では、使用が限定されほ
とんど利用されるに至ってない。
However, these foam molding resin compositions
Although there have been proposals for improving moldability, appearance, and flexibility, there have been almost no proposals for improving mechanical strength. In foam molded products, it is necessary that the air bubbles are uniformly dispersed in microscopic scales in order to achieve a uniform foaming state. In particular, if the bubbles are large, stress concentration occurs there, causing microcrazes and deterioration of physical properties. This is similar to the case where a particulate filler is dispersed in a resin, and it is presumed that stress is concentrated at the interface of the dispersed particles. For this reason, when a foam molded product is made lighter by increasing its foaming rate, the rigidity of the molded product tends to decrease. Therefore, foam molded products are of limited use in structural parts such as automobile parts and electrical parts, and are hardly ever used.

【0004】0004

【発明が解決しようとする課題】本発明は、上記の事情
に鑑みてなされたもので、物性の低下を抑え、そりや変
形などの外観品質の低下を極力おさえ構造部品として使
用可能な射出成形用の発泡用樹脂組成物とすることを目
的とする。
[Problems to be Solved by the Invention] The present invention has been made in view of the above circumstances, and provides injection molding that can be used as structural parts while suppressing deterioration of physical properties and minimizing deterioration of appearance quality such as warpage and deformation. The purpose is to create a foaming resin composition for use in

【0005】[0005]

【課題を解決するための手段】本発明の発泡用樹脂組成
物は、比表面積が9×103 cm3 /g以上の燃焼
灰を40重量%以下含む熱可塑性樹脂100重量部に対
して、化学発泡剤を0.05〜1.0重量部含んでなる
ことを特徴とする。燃焼灰は、比表面積が9×103 
cm3 /g以上の多孔質のものが使用される。燃焼灰
の比表面積が9×103 cm3 /g未満であると、
樹脂との密着性が低下して発泡成形体の物性が低下する
ので好ましくない。燃焼灰の粒径は重量平均粒径で1〜
20μmの範囲のものが発泡成形体中での分散性がよく
物性向上に寄与しやすくなるので好ましい。添加量は4
0重量%以下の充填量とする。添加量が40重量%を超
えると樹脂成分が少なくなり発泡しにくくなるので好ま
しくない。 さらにこの燃焼灰の一部を他のマイカ、タルクなどの充
填剤と併用することもできる。他の充填剤を燃焼灰と併
用する場合は、燃焼灰の添加量を超えない範囲で添加す
ることができる。充填剤の添加量が燃焼灰の量を超える
と燃焼灰の添加効果が消失して充填剤のみの場合の欠点
が発現するので好ましくない。すなわち、発泡成形体の
独立セルが大きくなり、そのため気泡に応力集中してミ
クロクレーズが発生して物性の低下を起こすこととなり
好ましくない。
[Means for Solving the Problems] The foaming resin composition of the present invention is a chemically foamed resin composition based on 100 parts by weight of a thermoplastic resin containing 40% by weight or less of combustion ash having a specific surface area of 9 x 103 cm3/g or more. It is characterized by containing 0.05 to 1.0 parts by weight of the agent. The specific surface area of combustion ash is 9×103
A porous material with a pore size of cm3/g or more is used. When the specific surface area of the combustion ash is less than 9 x 103 cm3/g,
This is not preferable because the adhesion with the resin decreases and the physical properties of the foamed molded product decrease. The particle size of combustion ash is 1 to 1 in terms of weight average particle size.
A thickness in the range of 20 μm is preferable because it has good dispersibility in the foamed molded product and easily contributes to improving the physical properties. The amount added is 4
The filling amount shall be 0% by weight or less. If the amount added exceeds 40% by weight, the resin component will decrease and foaming will become difficult, which is not preferable. Furthermore, a part of this combustion ash can also be used in combination with other fillers such as mica and talc. When other fillers are used together with combustion ash, they can be added in an amount that does not exceed the amount of combustion ash added. If the amount of filler added exceeds the amount of combustion ash, the effect of adding combustion ash will disappear and the disadvantages of using only filler will appear, which is not preferable. That is, the closed cells of the foamed molded product become large, which causes stress to concentrate on the bubbles and causes microcrazes, which is undesirable and causes deterioration of physical properties.

【0006】この燃焼灰は、流動床ボイラー、微粉炭ボ
イラーで可燃物を燃焼した際に発生する灰である。この
燃焼灰の灰分組成は、使用した可燃物により左右される
が、灰形状の安定性の点から石炭を10重量%以上含む
可燃物を燃焼した際に排出される灰であることが好まし
い。熱可塑性樹脂は射出成形できるものであれば、いず
れも使用できる。たとえば、ポリエチレン、ポリプロピ
レン、ポリスチレン、ABS、AS、ナイロン、ポリエ
ステル、塩化ビニル、などの単独または共重合体などの
公知の樹脂がいずれも使用できる。
[0006] This combustion ash is ash generated when combustible materials are burned in a fluidized bed boiler or a pulverized coal boiler. The ash composition of this combustion ash depends on the combustible material used, but from the viewpoint of stability of the ash shape, it is preferably ash that is discharged when a combustible material containing 10% by weight or more of coal is burned. Any thermoplastic resin that can be injection molded can be used. For example, any known resin such as a single or copolymer of polyethylene, polypropylene, polystyrene, ABS, AS, nylon, polyester, vinyl chloride, etc. can be used.

【0007】化学発泡剤は0.05〜1.0重量部の範
囲で熱可塑性樹脂100重量に対して添加するのが好ま
しい。0.05重量部以下ではほとんど樹脂発泡ができ
ないので好ましくない。一方1.0重量部を超えて添加
しても発泡倍率が増えないばかりか、成形後に成形品が
発泡し寸法安定性を維持できず物性低下をひきおこして
割れなどが起きるので好ましくない。
The chemical blowing agent is preferably added in an amount of 0.05 to 1.0 parts by weight per 100 parts by weight of the thermoplastic resin. If the amount is less than 0.05 part by weight, resin foaming will hardly be possible, which is not preferable. On the other hand, if it is added in an amount exceeding 1.0 parts by weight, not only will the expansion ratio not increase, but the molded product will foam after molding, making it impossible to maintain dimensional stability, resulting in deterioration of physical properties and cracking, which is not preferable.

【0008】また化学発泡剤は配合する樹脂と同種の樹
脂でマスターバッチ状にしたものが成形時ホッパー中で
の分散・取扱がよくなるので好ましい。この場合マスタ
ーバッチの使用量は化学発泡剤の含有量に応じて添加量
が決められる。たとえば、10重量部含有のマスターバ
ッチでは添加量は0.5〜10重量部の範囲となる。化
学発泡剤としては有機・無機のいずれも使用できる。例
えば、無機系としては、重炭酸ナトリウム、炭酸アンモ
ニウム、亜硝酸アンモニウム、ホウ水素化ナトリウムな
どが挙げられる。有機系としては、アゾジカルボンアミ
ド、アゾビスホルムアミド、イソブチロニトリル、ジア
ゾアミノベンゼンなどのアジド化合物、N、N’−ジニ
トロソペンタメチレンテトラミン、N、N’−ジニトロ
テレフタルアミド等のニトロソ化合物などが挙げられる
。さらに、これらの発泡剤の分解助剤として、一般に知
られている無機系のステアリン酸亜鉛、酢酸亜鉛、有機
系のグリセリン、ジエチレングリコール等および混合系
を用いてもよい。また、有機・無機発泡剤の混合系を用
いてもよい。
[0008] Furthermore, it is preferable that the chemical blowing agent be prepared in the form of a masterbatch using the same type of resin as the resin to be blended, since this facilitates dispersion and handling in the hopper during molding. In this case, the amount of masterbatch used is determined depending on the content of the chemical blowing agent. For example, in a masterbatch containing 10 parts by weight, the amount added is in the range of 0.5 to 10 parts by weight. Both organic and inorganic chemical blowing agents can be used. For example, inorganic systems include sodium bicarbonate, ammonium carbonate, ammonium nitrite, sodium borohydride, and the like. Examples of organic compounds include azide compounds such as azodicarbonamide, azobisformamide, isobutyronitrile, and diazoaminobenzene, and nitroso compounds such as N,N'-dinitrosopentamethylenetetramine and N,N'-dinitroterephthalamide. can be mentioned. Furthermore, as a decomposition aid for these blowing agents, generally known inorganic zinc stearate, zinc acetate, organic glycerin, diethylene glycol, etc., and mixed systems may be used. Further, a mixed system of organic and inorganic blowing agents may be used.

【0009】この組成物を形成するには、たとえば、燃
焼灰を通常の混合機を用いて熱可塑性樹脂と混合し、こ
れに化学発泡剤を添加するか、あるいは、3者を一緒に
混合してもよい。たとえば押出機やミキサーなどで混合
して成形される。この組成物には、酸化防止剤、滑剤、
着色剤、紫外線吸収剤、帯電防止剤、分散剤などを添加
することもできる。
[0009] To form this composition, for example, the combustion ash may be mixed with a thermoplastic resin using a conventional mixer, to which a chemical blowing agent may be added, or the three may be mixed together. It's okay. For example, they are mixed and molded using an extruder or mixer. The composition includes antioxidants, lubricants,
Colorants, ultraviolet absorbers, antistatic agents, dispersants, etc. can also be added.

【0010】0010

【発明の作用および効果】この発泡樹脂組成物は、充填
剤として特定性状の燃焼灰が特定量含まれている。この
燃焼灰は樹脂のマトリックス層に均一に分散して樹脂層
を補強している。このため発泡された成形品では樹脂の
マトリックス層が均一であるので、気泡が大きくならず
均一に分散できる。
Effects and Effects of the Invention This foamed resin composition contains a specific amount of combustion ash having specific properties as a filler. This combustion ash is uniformly dispersed in the resin matrix layer and reinforces the resin layer. For this reason, in a foamed molded product, the resin matrix layer is uniform, so the bubbles do not become large and can be uniformly dispersed.

【0011】従来の充填剤を含む発泡成形体では樹脂と
充填剤との密着性が悪いため、樹脂と充填剤との界面に
ボイドができやすい。そのため発泡圧がボイドの界面に
一気にかかり大きな気泡セルが発生するために曲げ弾性
率などの剛性の著しい低下をきたす。ところが本発明の
燃焼灰は、多孔質で樹脂との密着性がよいので上記のよ
うな大きなボイドはない。そして小さい気泡が多くかつ
均一に分散して発泡率を高め、かつ発泡成形体の物性の
低下が抑制できる。
[0011] In conventional foam molded articles containing fillers, the adhesion between the resin and the filler is poor, so voids are likely to form at the interface between the resin and the filler. Therefore, foaming pressure is applied all at once to the void interface, generating large bubble cells, resulting in a significant decrease in rigidity such as flexural modulus. However, the combustion ash of the present invention is porous and has good adhesion to the resin, so there are no large voids as described above. In addition, many small bubbles are uniformly dispersed, increasing the foaming rate and suppressing deterioration of the physical properties of the foam molded product.

【0012】この結果、軽量化できかつ高い剛性を示す
ので構造部品として自動車などに使用できる、発泡射出
成形品が得られる。
[0012] As a result, a foam injection molded product can be obtained which can be used as a structural part in automobiles and the like because it is lightweight and exhibits high rigidity.

【0013】[0013]

【実施例】以下、実施例により具体的に説明する。熱可
塑性樹脂としてポリプロピレン樹脂(商品名J−200
3G、出光石油化学(株)社製)85重量部に、比表面
積が1.3×104 cm3 /gの平均粒径4.9μ
mで組成を表1に示す燃焼灰15重量部との混合物に化
学発泡剤を1.5重量部添加してNo.1の発泡樹脂組
成物とした。ポリプロピレン樹脂80重量
[Examples] Hereinafter, the present invention will be explained in detail using examples. Polypropylene resin (product name J-200) is used as a thermoplastic resin.
3G, manufactured by Idemitsu Petrochemical Co., Ltd.) to 85 parts by weight, a specific surface area of 1.3 x 104 cm3/g and an average particle size of 4.9μ
1.5 parts by weight of a chemical blowing agent was added to a mixture with 15 parts by weight of combustion ash whose composition is shown in Table 1. The foamed resin composition was prepared as No. 1 foamed resin composition. Polypropylene resin 80 weight

【0014】[0014]

【表1】 部、燃焼灰15重量部、マイカ5重量部との混合物に化
学発泡剤を1.5重量部添加してNo.2の発泡樹脂組
成物とした。比較としてポリプロピレン樹脂80重量部
、燃焼灰の変わりに公知の充填剤のタルク20重量部と
の混合物に化学発泡剤を1.5重量部添加してNo.3
の発泡樹脂組成物とした。但し、化学発泡剤はポリスレ
ンEE−205(6)(永和化成(株)製)を用いた。 これはLDPEをキャリアレジンとする10重量%のマ
スターバッチで、分解温度160〜220℃である。こ
の3種の樹脂組成物を樹脂温度を変えて射出成形してそ
の発泡率を調べた。
[Table 1] 1.5 parts by weight of a chemical blowing agent was added to a mixture of 15 parts by weight of combustion ash and 5 parts by weight of mica. A foamed resin composition of No. 2 was prepared. For comparison, No. 1 was prepared by adding 1.5 parts by weight of a chemical blowing agent to a mixture of 80 parts by weight of polypropylene resin and 20 parts by weight of talc, a known filler instead of combustion ash. 3
A foamed resin composition was prepared. However, polysrene EE-205(6) (manufactured by Eiwa Kasei Co., Ltd.) was used as the chemical blowing agent. This is a 10% by weight masterbatch using LDPE as a carrier resin and has a decomposition temperature of 160-220°C. These three types of resin compositions were injection molded at different resin temperatures and their foaming rates were examined.

【0015】発泡率=1−(発泡後の成形品の重量)/
(発泡無し成形品の重量)である。 表2に得られた成形体の比重を示す。この比重の測定は
上記の温度で成形した成形品より試験片を切り出し、A
STM−D792に基づいて測定した。この比重をもと
に発泡率を算出した。図1に成形温度と発泡率との関係
のグラグを示す。燃焼灰を含まないNo.3は発泡率が
低い。一方燃焼灰を使用したNo.1、2は発泡率が高
くなっており発泡性が良いことを示している。
[0015] Foaming rate=1-(weight of molded product after foaming)/
(Weight of molded product without foaming). Table 2 shows the specific gravity of the molded product obtained. To measure this specific gravity, cut out a test piece from the molded product molded at the above temperature, and
Measured based on STM-D792. The foaming rate was calculated based on this specific gravity. Figure 1 shows a graph of the relationship between molding temperature and foaming rate. No. containing no combustion ash. 3 has a low foaming rate. On the other hand, No. 1 using combustion ash. Nos. 1 and 2 have a high foaming rate, indicating good foamability.

【0016】さらに、上記の成形品の曲げ弾性率を(A
STM−D790に基づき)測定し
Furthermore, the bending elastic modulus of the above molded article is (A
(Based on STM-D790)

【0017】[0017]

【表2】 発泡率との関係を図2の線グラフで示した。燃焼灰を含
まないNo.3に比べてNo.1、2は弾性率が著しく
向上していることを示している。すなわち、燃焼灰を含
む場合は、発泡率が大きくなり、従来の充填剤のものに
比べて物性も向上していることを示している。No.2
の燃焼灰にさらにマイカを添加することにより発泡率お
よび物性ともに向上していることを示している。
[Table 2] The relationship with foaming rate is shown in the line graph of FIG. No. containing no combustion ash. No.3 compared to No.3. 1 and 2 indicate that the elastic modulus is significantly improved. That is, when combustion ash is included, the foaming rate increases and the physical properties are also improved compared to those using conventional fillers. No. 2
This shows that both the foaming rate and physical properties are improved by adding mica to the combustion ash.

【0018】また図3にNo.1とNo.3を210℃
で射出成形した成形品の8倍に拡大した厚み2mmの断
面の模式図を示す。No.3の充填剤にタルクを用いた
もの(b)では、大きな気泡が存在しているが、No.
1の燃焼灰を含むもの(a)では、燃焼灰の樹脂中での
分散性がよいので気泡が大きくならず、小気泡で均一に
広がっておりそのため機械的強度の低下が少ないものと
推定される。
[0018] Also, in Fig. 3, No. 1 and no. 3 at 210℃
This is a schematic diagram of a 2 mm thick cross section of a molded product injection molded in 8 times enlarged. No. In No. 3 (b), in which talc was used as the filler, large air bubbles were present;
In case 1 (a) containing combustion ash, the combustion ash has good dispersibility in the resin, so the bubbles do not become large, and the small bubbles are spread uniformly, so it is presumed that there is little decrease in mechanical strength. Ru.

【図面の簡単な説明】[Brief explanation of the drawing]

【図1】  発泡成形樹脂温度と発泡率との関係のグラ
フ。
FIG. 1 is a graph of the relationship between foam molding resin temperature and foaming rate.

【図2】  発泡率と曲げ弾性率との関係のグラフ。FIG. 2 is a graph of the relationship between foaming rate and flexural modulus.

【図3】  発泡成形体の気泡の状態を示す模式図。FIG. 3 is a schematic diagram showing the state of bubbles in a foamed molded product.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】  比表面積が9×103 cm3 /g
以上の燃焼灰を40重量%以下含む熱可塑性樹脂100
重量部に対して、化学発泡剤を0.05〜1.0重量部
含んでなることを特徴とする発泡用樹脂組成物。
[Claim 1] Specific surface area is 9×103 cm3/g
Thermoplastic resin 100 containing 40% by weight or less of combustion ash of
A foaming resin composition comprising 0.05 to 1.0 parts by weight of a chemical foaming agent.
JP3033143A 1991-02-27 1991-02-27 Foaming resin composition Expired - Fee Related JP2589222B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3033143A JP2589222B2 (en) 1991-02-27 1991-02-27 Foaming resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3033143A JP2589222B2 (en) 1991-02-27 1991-02-27 Foaming resin composition

Publications (2)

Publication Number Publication Date
JPH04272939A true JPH04272939A (en) 1992-09-29
JP2589222B2 JP2589222B2 (en) 1997-03-12

Family

ID=12378368

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3033143A Expired - Fee Related JP2589222B2 (en) 1991-02-27 1991-02-27 Foaming resin composition

Country Status (1)

Country Link
JP (1) JP2589222B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017206624A (en) * 2016-05-19 2017-11-24 富士高分子工業株式会社 Normal temperature thermally conductive and high temperature adiabatic composition
JP2020075997A (en) * 2018-11-07 2020-05-21 株式会社日本触媒 Composite material and production method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1248618C (en) 2001-03-19 2006-04-05 西铁城钟表株式会社 Length adjustment device of band-shaped ornament

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6339932A (en) * 1986-08-05 1988-02-20 Mitsubishi Petrochem Co Ltd Expandable resin composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6339932A (en) * 1986-08-05 1988-02-20 Mitsubishi Petrochem Co Ltd Expandable resin composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017206624A (en) * 2016-05-19 2017-11-24 富士高分子工業株式会社 Normal temperature thermally conductive and high temperature adiabatic composition
JP2020075997A (en) * 2018-11-07 2020-05-21 株式会社日本触媒 Composite material and production method thereof

Also Published As

Publication number Publication date
JP2589222B2 (en) 1997-03-12

Similar Documents

Publication Publication Date Title
US6723793B2 (en) Blends of ethylenic polymers with improved modulus and melt strength and articles fabricated from these blends
US5567742A (en) Dimensionally-stable polypropylene foam expanded with inorganic blowing agents
US5366675A (en) Foamable polyethylene-based composition for rotational molding
EP1373401B1 (en) Blends of ethylenic polymers with improved modulus and melt strength and articles fabricated from these blends
CA2128007C (en) Dimensionally-stable polypropylene foam expanded with inorganic blowing agents
JPS6245256B2 (en)
JP2002275298A (en) Open-cell foam of polyethylene resin composition
JPH04272939A (en) Foamable resin composition
JPH09202837A (en) Foamed particle of electrically conductive polypropylene resin and its production
JPS60252636A (en) Preparation of preexpanded particle
JP4231251B2 (en) Polypropylene resin pre-expanded particles and in-mold expanded molded articles using the same
JP3674832B2 (en) Wood powder highly filled foamable resin composition and foamed molded article
JPH061874A (en) Preexpanded polyethylene resin particle
JP4196238B2 (en) Foaming agent composition and method for producing thermoplastic resin foam
JPH07228721A (en) Production of polypropylene resin foam particle
JPS5827726A (en) Foamed rubber-modified styrene resin composition
JP2023146523A (en) Expandable resin composition, expandable resin molded body and production method of the same
JPH06172572A (en) Cycloolefin resin foam
JP4306059B2 (en) Thermoplastic elastomer composition and foam
JP3463978B2 (en) Foam molding material
JP3307670B2 (en) Method for producing thermoplastic polyester elastomer foam
JP3628169B2 (en) Method for producing polyolefin resin pre-expanded particles
JPS60110733A (en) Expandable polyolefin resin composition
JPH0547578B2 (en)
JPH02284933A (en) Production of foamed styrene resin board

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees