JPH04345635A - Lightweight resin molding and its production - Google Patents
Lightweight resin molding and its productionInfo
- Publication number
- JPH04345635A JPH04345635A JP3148026A JP14802691A JPH04345635A JP H04345635 A JPH04345635 A JP H04345635A JP 3148026 A JP3148026 A JP 3148026A JP 14802691 A JP14802691 A JP 14802691A JP H04345635 A JPH04345635 A JP H04345635A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- foaming
- weight
- expansion ratio
- molding
- 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
- 229920005989 resin Polymers 0.000 title claims abstract description 52
- 239000011347 resin Substances 0.000 title claims abstract description 52
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000000465 moulding Methods 0.000 title abstract description 13
- 239000004604 Blowing Agent Substances 0.000 claims abstract description 14
- 229920005990 polystyrene resin Polymers 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 238000005187 foaming Methods 0.000 claims description 21
- 229920001955 polyphenylene ether Polymers 0.000 claims description 13
- 238000010097 foam moulding Methods 0.000 claims description 11
- 239000004088 foaming agent Substances 0.000 claims description 11
- 239000006260 foam Substances 0.000 claims description 8
- -1 polyphenylene Polymers 0.000 abstract description 8
- 238000000034 method Methods 0.000 abstract description 5
- 229920000265 Polyparaphenylene Polymers 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 7
- 239000011324 bead Substances 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 4
- 239000000470 constituent Substances 0.000 description 3
- 239000013585 weight reducing agent Substances 0.000 description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- QQOMQLYQAXGHSU-UHFFFAOYSA-N 2,3,6-Trimethylphenol Chemical compound CC1=CC=C(C)C(O)=C1C QQOMQLYQAXGHSU-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、装置類の構成材として
適用可能な1.5ないし15倍程度の低発泡倍率で十分
な強度を有する軽量樹脂成形体ならびにかかる成形体を
短時間で製造し得る製造方法に関する。[Industrial Application Field] The present invention is directed to a lightweight resin molded article that has sufficient strength at a low expansion ratio of about 1.5 to 15 times and can be used as a constituent material for equipment, and to produce such a molded article in a short time. The present invention relates to a possible manufacturing method.
【0002】0002
【従来の技術】近年、省エネルギーの観点から、自動車
の重量を軽減して燃料消費率を向上せしめる努力が続け
られている。金属材料を樹脂成形品に置換することによ
り軽量化が図られているが、さらにより軽量化された構
造材を得るために、薄肉成形が採用される機運にある。
しかし、大型成形品では中空となるものが多いため、強
度的に限度があり、極端な薄肉化は困難である。2. Description of the Related Art In recent years, from the viewpoint of energy conservation, efforts have been made to reduce the weight of automobiles and improve their fuel consumption rates. Weight reduction has been achieved by replacing metal materials with resin molded products, but thin-walled molding is now being adopted in order to obtain even lighter structural materials. However, since many large molded products are hollow, there is a limit to their strength, and it is difficult to make them extremely thin.
【0003】このような薄肉成形に代えて発泡成形が注
目されている。発泡による成形体の軽量化は、機能性樹
脂、すなわちエンジニアリングプラスチックといわれて
いる各種樹脂類の機械的ないしは物理的特性を発揮する
状態で行なわれなければならない。Foam molding is attracting attention as an alternative to such thin wall molding. Reducing the weight of a molded article by foaming must be carried out in a state that exhibits the mechanical or physical properties of functional resins, that is, various resins called engineering plastics.
【0004】従来行なわれていた、単に化学的または物
理的な発泡剤を基材樹脂に混合することによって射出成
形を行なう発泡成形では、たかだか5ないし10%の軽
量化が達せられるにすぎない。大幅な軽量化を達成する
ためには、ポリスチレンのビーズを用いた、いわゆる型
物の発泡成形が有効であることが知られている。しかし
、従来のポリスチレンの発泡成形体は、発泡倍率が40
ないし100倍程度の高発泡が多く、構造剤としての十
分な強度を得ることができなかった。[0004] Conventional foam molding, in which injection molding is carried out simply by mixing a chemical or physical blowing agent with a base resin, can only achieve a weight reduction of 5 to 10% at most. It is known that foam molding using polystyrene beads is effective in achieving significant weight reduction. However, conventional polystyrene foam moldings have an expansion ratio of 40.
There were many cases of high foaming of about 100 to 100 times, and it was not possible to obtain sufficient strength as a structuring agent.
【0005】もし、構造材として十分な強度を保持し得
る、例えば15倍程度の比較的低い発泡倍率の発泡成形
を行なおうとすると、従来2分程度であった成形時間が
10ないし20分のように長くなり、生産性が大幅に低
下する。この傾向は、発泡倍率の低い樹脂成形体を得よ
うとすればするほど著しくなる。If one attempts to carry out foam molding at a relatively low expansion ratio of, for example, about 15 times, which can maintain sufficient strength as a structural material, the molding time, which conventionally takes about 2 minutes, will take 10 to 20 minutes. This results in a long process and a significant drop in productivity. This tendency becomes more pronounced the more one attempts to obtain a resin molded article with a lower expansion ratio.
【0006】[0006]
【発明が解決しようとする課題】本発明は、構成材とし
も適用可能な機械的または物理的特性を保持する比較的
低倍率の発泡状態にある軽量樹脂成形体を提供すること
、並びにそのような軽量樹脂成形体を製造する方法を提
供することことを課題とする。SUMMARY OF THE INVENTION It is an object of the present invention to provide a lightweight resin molded article in a foamed state with a relatively low magnification that maintains mechanical or physical properties that can be used as a constituent material. An object of the present invention is to provide a method for manufacturing a lightweight resin molded body.
【0007】[0007]
【課題を解決するための手段】この課題は、ポリスチレ
ン系樹脂95ないし5重量%とポリフェニレンエーテル
系樹脂5ないし95重量%とを混合した基材樹脂に対し
て、3重量%以下の発泡剤を含有させて発泡加工し、1
.5ないし15倍の発泡倍率に形成された、軽量樹脂発
泡成形体、並びに、ポリスチレン系樹脂95ないし5重
量%とポリフェニレンエーテル系樹脂5ないし95重量
%とからなる基材樹脂を予備発泡せしめ、その後該予備
発泡の行なわれている基材樹脂に対して、3重量%以下
の発泡剤を混合し、所望型内で1.5ないし15倍の低
発泡倍率の二次発泡成形を行なう、軽量樹脂発泡成形体
の製造方法によって解決される。[Means for Solving the Problem] This problem is achieved by adding 3% by weight or less of a blowing agent to a base resin that is a mixture of 95 to 5% by weight of a polystyrene resin and 5 to 95% by weight of a polyphenylene ether resin. 1.
.. A lightweight resin foam molded body formed with an expansion ratio of 5 to 15 times, and a base resin consisting of 95 to 5% by weight of polystyrene resin and 5 to 95% by weight of polyphenylene ether resin are pre-foamed, and then A lightweight resin that is prepared by mixing 3% by weight or less of a blowing agent with the pre-foamed base resin and performing secondary foam molding at a low expansion ratio of 1.5 to 15 times in a desired mold. The problem is solved by a method for manufacturing a foam molded article.
【0008】本発明において用いられるポリスチレン系
樹脂とは、ポリスチレン、ポリスチレン−ブタジエン共
重合体、ポリスチレン−アクリロニトリル共重合体、ス
チレンのグラフト共重合体等のように、スチレンを主成
分とする重合樹脂および共重合樹脂等を総称するもので
ある。また、これらを主成分とする多樹脂との混合樹脂
をも含むものである。The polystyrene resin used in the present invention refers to polymer resins containing styrene as a main component, such as polystyrene, polystyrene-butadiene copolymer, polystyrene-acrylonitrile copolymer, styrene graft copolymer, etc. It is a general term for copolymer resins, etc. It also includes mixed resins with multiple resins containing these as main components.
【0009】また、本発明において使用されるポリフェ
ニレンエーテル系樹脂とは、一般式[0009] The polyphenylene ether resin used in the present invention has the general formula
【化1】
(ここに、R1、R2、R3およびR4は、それぞれ独
立して、水素原子、ハロゲン原子、アルキル基、アルコ
キシ基およびハロゲン原子とフェニル環との間に、少な
くとも2個の炭素原子を有するハロアルキル基またはハ
ロアルコキシ基で第3α−炭素を含まないものから選ば
れた一価置換基を表わし、またnは重合度を表わす整数
である)で表わされる重合体の総称であって、上記一般
式(化1)で表わされる重合体の一種単独であっても、
2種以上が組み合わされた共重合体であってもよい。好
ましい具体例では、R1 およびR2が炭素原子数1な
いし4のアルキル基であり、R3およびR4が水素原子
もしくは炭素原子数1ないし4のアルキル基である。例
えば、ポリ(2,6−ジメチル−1,4−フェニレン)
エーテル、ポリ(2,6−ジエチル−1,4−フェニレ
ン)エーテル、ポリ(2−メチル−6−エチル−1,4
−フェニレン)エーテル、ポリ(2−メチル−6−プロ
ピル−1,4−フェニレン)エーテル、ポリ(2,6−
ジプロピル−1,4−フェニレン)エーテル、ポリ(2
−エチル−6−プロピル−1,4−フェニレン)エーテ
ルなどが挙げられる。(Here, R1, R2, R3 and R4 are each independently a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and at least two carbon atoms between the halogen atom and the phenyl ring) represents a monovalent substituent selected from a haloalkyl group or a haloalkoxy group having a tertiary α-carbon, and n is an integer representing the degree of polymerization), Even if one kind of the polymer represented by the above general formula (Chemical formula 1) is used alone,
It may also be a copolymer in which two or more types are combined. In a preferred embodiment, R1 and R2 are C1-C4 alkyl groups, and R3 and R4 are hydrogen atoms or C1-C4 alkyl groups. For example, poly(2,6-dimethyl-1,4-phenylene)
Ether, poly(2,6-diethyl-1,4-phenylene) ether, poly(2-methyl-6-ethyl-1,4)
-phenylene) ether, poly(2-methyl-6-propyl-1,4-phenylene) ether, poly(2,6-
dipropyl-1,4-phenylene) ether, poly(2
-ethyl-6-propyl-1,4-phenylene) ether and the like.
【0010】また、PPE共重合体としては、上記ポリ
フェニレンエーテル繰り返し単位中にアルキル三置換フ
ェノール、例えば2,3,6−トリメチルフェノールを
一部含有する共重合体を挙げることができる。また、こ
れらのPPEにスチレン系化合物がグラフトした共重合
体であってもよい。Examples of the PPE copolymer include copolymers containing a portion of alkyl trisubstituted phenol, such as 2,3,6-trimethylphenol, in the polyphenylene ether repeating unit. Moreover, a copolymer obtained by grafting a styrene compound onto these PPEs may also be used.
【0011】本発明の基材樹脂は、ポリスチレン系樹脂
95ないし5重量%に対してポリフェニレンエーテル系
樹脂5ないし95重量%を混合したものである。PS樹
脂に適宜量のPPE樹脂を混合することにより所望の発
泡倍率を得ることができる。上述の範囲において、1.
5ないし15倍程度の比較的低い発泡倍率を達成するこ
とができる。The base resin of the present invention is a mixture of 95 to 5% by weight of a polystyrene resin and 5 to 95% by weight of a polyphenylene ether resin. A desired expansion ratio can be obtained by mixing an appropriate amount of PPE resin with the PS resin. In the above range, 1.
Relatively low expansion ratios of the order of 5 to 15 times can be achieved.
【0012】PPE樹脂が、5重量%未満になると所望
の低発泡倍率で止めることが困難になる。短時間で成形
しようとすると高発泡倍率、例えば30倍程度になり、
所望強度が得られなくなる。なお、成形温度を低下せし
め、長時間成形を行うことにより低発泡倍率とすること
は可能であるが、生産性が低くなり、当然生産コストは
上昇せざるを得ない。[0012] When the PPE resin is less than 5% by weight, it becomes difficult to maintain the desired low expansion ratio. If you try to mold it in a short time, the expansion ratio will be high, for example around 30 times,
Desired strength cannot be obtained. Although it is possible to achieve a low foaming ratio by lowering the molding temperature and performing molding for a longer time, the productivity will be lower and production costs will inevitably increase.
【0013】上記とは逆に、ポリフェニレンエーテル系
樹脂を95重量%よりも多く混合した樹脂を基材とした
場合には、発泡のために必要とする温度が急激に高くな
るため、所要時間も長くなり、設備費をも含めて、生産
コストが上昇する。In contrast to the above, when the base material is a resin containing more than 95% by weight of polyphenylene ether resin, the temperature required for foaming increases rapidly, and the time required for foaming also increases. This increases production costs, including equipment costs.
【0014】本発明においては、基材樹脂の発泡剤含有
率は、3重量%以下でなければならない。ここでいう発
泡剤含有率とは、発泡成形における予備発泡(一次発泡
)を終え、実用上必要とされる製品の形を作る、いわゆ
る発泡成形(又は二次成形)の前における発泡剤の含有
量をいう。なお、予備発泡前の発泡剤の含有率は実際上
任意であるが、工業的生産上のコストを考慮すると7%
以下であることが望ましい。In the present invention, the foaming agent content of the base resin must be 3% by weight or less. The blowing agent content here refers to the content of the blowing agent after the pre-foaming (primary foaming) in foam molding and before the so-called foam molding (or secondary molding) that creates the shape of the product that is practically required. Refers to quantity. The content of the blowing agent before pre-foaming is practically arbitrary, but considering the cost of industrial production, it is set at 7%.
The following is desirable.
【0015】このように、予備発泡が終わり発泡成形を
行なう前の基材樹脂における発泡剤含有率が3重量%以
下であることが、低発泡成形体を短い成形サイクルで製
造することを特徴とする本発明においては特に重要であ
る。さらに、3重量%以上では、長期間の寸法安定性が
悪く、常温放置で5/1000以上の寸法変化が認めら
れる。これに対して本発明のように発泡剤含有率を3重
量%以下にすることによって、1/1000以下の寸法
変化に抑制されることが確認された。[0015] As described above, the characteristic that the foaming agent content in the base resin after pre-foaming and before foam molding is 3% by weight or less is that a low-foam molded article can be produced in a short molding cycle. This is particularly important in the present invention. Further, if the content is 3% by weight or more, long-term dimensional stability is poor, and a dimensional change of 5/1000 or more is observed when left at room temperature. On the other hand, it was confirmed that by setting the blowing agent content to 3% by weight or less as in the present invention, the dimensional change was suppressed to 1/1000 or less.
【0016】[0016]
【実施例】以下、実施例に即して本発明の内容を開示す
る。図1は発泡剤の含有率を横軸にとり、発泡倍率を縦
軸とするグラフである。図から明らかなように、発泡剤
の含有量が3重量%以上では、たとえPS系樹脂にPP
E系樹脂を混合したとしても急激な発泡が生じ、結果的
に高発泡となる。しかし、発泡剤の含有率が3重量%以
下になると発泡速度が緩やかになり、制御し易くなる。
この場合の発泡は、均一な微細独立気泡で、構造体とし
て必要な1.5ないし15倍の低発泡倍率の成形体を得
ることができる。このような比較的低い発泡倍率の成形
体は自動車をはじめ、家電製品、OA機器等の構成材と
して有用であり、工業的にも利用価値が高いものである
。[Examples] The contents of the present invention will be disclosed below with reference to Examples. FIG. 1 is a graph in which the horizontal axis represents the foaming agent content and the vertical axis represents the foaming ratio. As is clear from the figure, if the blowing agent content is 3% by weight or more, even if the PS resin contains PP.
Even when E-based resin is mixed, rapid foaming occurs, resulting in high foaming. However, when the content of the foaming agent is 3% by weight or less, the foaming speed becomes slower and easier to control. In this case, the foaming can produce a molded article with uniform fine closed cells and a low expansion ratio of 1.5 to 15 times, which is necessary for a structural body. Molded bodies with such a relatively low expansion ratio are useful as constituent materials for automobiles, home appliances, office automation equipment, etc., and have high industrial utility value.
【0017】本発明の実施例においては、基材樹脂とし
てポリスチレン樹脂とポリフェニレンエーテル樹脂とを
、表1に示す割合で混合したものを使用した。この基材
樹脂からなるビーズに対して、発泡剤であるn−ブタン
を表1に示した比率となるように含浸させた。In the examples of the present invention, a mixture of polystyrene resin and polyphenylene ether resin in the proportions shown in Table 1 was used as the base resin. The beads made of this base resin were impregnated with n-butane, which is a foaming agent, at the ratio shown in Table 1.
【表1】[Table 1]
【0018】このように形成されたビーズを、表1に示
すように水蒸気によって2分間加熱し、予備発泡ビーズ
を得た。この予備発泡ビーズの発泡倍率および発泡剤の
含有量は表1に示す通りである。The beads thus formed were heated with water vapor for 2 minutes as shown in Table 1 to obtain pre-foamed beads. The expansion ratio and foaming agent content of the pre-expanded beads are shown in Table 1.
【0019】さらに、上記予備発泡ビーズを表1に記し
た成形条件の下に発泡加工(二次発泡)させ、この場合
野発泡倍率と、発泡剤の含有量および成形品外観とを評
価した。Furthermore, the above pre-expanded beads were subjected to foaming processing (secondary foaming) under the molding conditions shown in Table 1, and the initial foaming ratio, foaming agent content, and appearance of the molded product were evaluated.
【0020】さらに、このようにして得られた成形品を
表1に示すような条件により熱風オーブン中で10時間
熟成し、同じく発泡倍率、発泡剤の含有量、および成形
品外観を評価した。Furthermore, the molded product thus obtained was aged in a hot air oven for 10 hours under the conditions shown in Table 1, and the expansion ratio, foaming agent content, and appearance of the molded product were similarly evaluated.
【0021】なお、発泡倍率は、基材樹脂の比重(=1
.06)を成形品の比重で除すことにより求めた。また
、発泡剤の含有量は、250度Cで10分間加熱した場
合の揮発減量率をいう。Note that the expansion ratio is based on the specific gravity of the base resin (=1
.. 06) by the specific gravity of the molded article. Moreover, the content of the foaming agent refers to the volatilization loss rate when heated at 250 degrees C for 10 minutes.
【0022】比較例1、2は、基材樹脂の組成が本発明
の範囲外である場合、また、比較例3、4は、発泡成形
時の発泡剤の含有量が本発明の範囲外である場合を示し
たものである。Comparative Examples 1 and 2 are cases where the composition of the base resin is outside the range of the present invention, and Comparative Examples 3 and 4 are cases where the content of the blowing agent during foam molding is outside the range of the invention. This shows a certain case.
【0023】[0023]
【発明の効果】本発明によれば、従来のポリスチレン樹
脂発泡成形体の1.5ないし15倍の低発泡成形体を得
るのに必要な成形時間を大幅に短縮することができ、か
つ発泡状態が安定したことから、生産性が著しく向上し
た。さらに、ポリフェニレンエーテル樹脂を混合したこ
とから、耐熱性の向上が図れた。また、発泡剤の使用量
を低減することができ、また、用途如何によっては、熟
成工程を省略することも可能であり、かかる点からも生
産性の向上に寄与することができる。Effects of the Invention According to the present invention, the molding time required to obtain a low-foam molded product 1.5 to 15 times that of conventional polystyrene resin foam molded products can be significantly shortened, and the foamed state can be reduced. As a result, productivity has improved significantly. Furthermore, since polyphenylene ether resin was mixed, heat resistance was improved. Furthermore, the amount of blowing agent used can be reduced, and depending on the application, it is also possible to omit the aging step, which can also contribute to improving productivity.
【0024】なお、本発明にかかる軽量樹脂発泡成形体
は、使用する発泡剤を低減させており、残留発泡材含有
量も減少していることから、二次成形後の常温放置およ
び熱風オーブンによる熟成後における長期寸法安定性も
格段に向上する。かかる特性は、大型成形体、例えば自
動車の計器板(インパネ)のような全長の長い部品を製
作する場合にあっては、特に重要である。従来のような
長期寸法変化の大きい成形品にあっては、製造後所定部
位に取り付けるまでに、長期間にわたる安定化時間が必
要であった。それに対し、本発明にかかる軽量樹脂成形
体では、長期寸法安定性が大幅に向上し、その寸法変化
、主として収縮は、従来の数分の1程度となる利点が得
られる。[0024] The lightweight resin foam molded article according to the present invention uses less blowing agent and has a lower residual foaming material content, so it can be left at room temperature or heated in a hot air oven after secondary molding. Long-term dimensional stability after aging is also significantly improved. Such characteristics are particularly important when producing large molded objects, for example, parts with a long overall length such as an automobile instrument panel. Conventional molded products that undergo large long-term dimensional changes require a long period of stabilization time after manufacture before being attached to a predetermined location. In contrast, the lightweight resin molded article according to the present invention has the advantage that its long-term dimensional stability is greatly improved, and its dimensional change, mainly shrinkage, is about a fraction of that of conventional products.
【図1】 発泡剤の含有量と発泡倍率との関係を示す
グラフである。FIG. 1 is a graph showing the relationship between foaming agent content and foaming ratio.
Claims (2)
重量%とポリフェニレンエーテル系樹脂5ないし95重
量%とを混合した基材樹脂に対して、3重量%以下の発
泡剤を含有させて発泡加工し、1.5ないし15倍の発
泡倍率に形成されたことを特徴とする軽量樹脂発泡成形
体。[Claim 1] Polystyrene resin 95 to 5
The base resin is a mixture of 5% to 95% by weight of polyphenylene ether resin and 3% by weight or less of a foaming agent to form a foaming ratio of 1.5 to 15 times. A lightweight resin foam molded product characterized by:
重量%とポリフェニレンエーテル系樹脂5ないし95重
量%とからなる基材樹脂を予備発泡せしめ、その後該予
備発泡の行なわれている基材樹脂に対して、3重量%以
下の発泡剤を混合し、所望型内で1.5ないし15倍の
低発泡倍率の二次発泡成形を行なうことを特徴とする軽
量樹脂発泡成形体の製造方法。[Claim 2] Polystyrene resin 95 to 5
Pre-foaming a base resin consisting of 5 to 95 wt% of a polyphenylene ether resin, and then mixing 3 wt% or less of a blowing agent with respect to the pre-foamed base resin; A method for producing a lightweight resin foam molded article, which comprises performing secondary foam molding at a low expansion ratio of 1.5 to 15 times in a desired mold.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148026A JP2511743B2 (en) | 1991-05-23 | 1991-05-23 | Lightweight resin molding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148026A JP2511743B2 (en) | 1991-05-23 | 1991-05-23 | Lightweight resin molding |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04345635A true JPH04345635A (en) | 1992-12-01 |
JP2511743B2 JP2511743B2 (en) | 1996-07-03 |
Family
ID=15443454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3148026A Expired - Fee Related JP2511743B2 (en) | 1991-05-23 | 1991-05-23 | Lightweight resin molding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2511743B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003078517A3 (en) * | 2002-03-20 | 2004-02-05 | Polimeri Europa Spa | Compositions based on expandable vinylaromatic polymers with an improved expandability |
GB2453512A (en) * | 2007-10-08 | 2009-04-15 | Gurit | Composite laminated articles having foam cores |
US8465832B2 (en) | 2007-10-08 | 2013-06-18 | Gurit (Uk) Ltd. | Composite laminated article and manufacture thereof |
JP2017088834A (en) * | 2015-11-17 | 2017-05-25 | 旭化成株式会社 | Expanded material |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63150337A (en) * | 1986-10-27 | 1988-06-23 | ゼネラル・エレクトリック・カンパニイ | Low density particle of polyphenylene ether resin |
JPH02218727A (en) * | 1988-11-14 | 1990-08-31 | Mitsui Toatsu Chem Inc | Production of heat-resistant foamed sheet |
-
1991
- 1991-05-23 JP JP3148026A patent/JP2511743B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63150337A (en) * | 1986-10-27 | 1988-06-23 | ゼネラル・エレクトリック・カンパニイ | Low density particle of polyphenylene ether resin |
JPH02218727A (en) * | 1988-11-14 | 1990-08-31 | Mitsui Toatsu Chem Inc | Production of heat-resistant foamed sheet |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003078517A3 (en) * | 2002-03-20 | 2004-02-05 | Polimeri Europa Spa | Compositions based on expandable vinylaromatic polymers with an improved expandability |
CN100408617C (en) * | 2002-03-20 | 2008-08-06 | 波利玛利欧洲股份公司 | Compositions based on expandable vinylaromatic polymers with an improved expandability |
GB2453512A (en) * | 2007-10-08 | 2009-04-15 | Gurit | Composite laminated articles having foam cores |
GB2453512B (en) * | 2007-10-08 | 2009-11-25 | Gurit | Composite laminated article and manufacture thereof |
US8465832B2 (en) | 2007-10-08 | 2013-06-18 | Gurit (Uk) Ltd. | Composite laminated article and manufacture thereof |
JP2017088834A (en) * | 2015-11-17 | 2017-05-25 | 旭化成株式会社 | Expanded material |
Also Published As
Publication number | Publication date |
---|---|
JP2511743B2 (en) | 1996-07-03 |
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