JPS6055290B2 - Method for manufacturing polyethylene foam - Google Patents
Method for manufacturing polyethylene foamInfo
- Publication number
- JPS6055290B2 JPS6055290B2 JP54104626A JP10462679A JPS6055290B2 JP S6055290 B2 JPS6055290 B2 JP S6055290B2 JP 54104626 A JP54104626 A JP 54104626A JP 10462679 A JP10462679 A JP 10462679A JP S6055290 B2 JPS6055290 B2 JP S6055290B2
- Authority
- JP
- Japan
- Prior art keywords
- density polyethylene
- melting point
- foam
- density
- less
- 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
Links
Classifications
-
- B29C47/92—
Landscapes
- 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)
Description
【発明の詳細な説明】
本発明は、ポリエチレン発泡体の製造方法に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing polyethylene foam.
従来、熱可塑性樹脂を発泡させる方法としては、熱可塑
性樹脂と揮発性液体とを高圧高圧下に混合し、低圧帯域
へ押出して発泡させる方法が知られている。Conventionally, as a method for foaming a thermoplastic resin, a method is known in which a thermoplastic resin and a volatile liquid are mixed under high pressure and extruded into a low pressure zone to foam.
しカルながら、この方法はポリエチレンを発泡させると
、発泡体の気泡は大部分独立しており、フィルター等通
気性を要求される用途には全く通さない。本発明者は、
かかる欠点を改良する方法について鋭意研究した結果、
低密度ポリエチレン及び高密度ポリエチレンのメルトイ
ンデックス、混合比率、押出温度を特定することにより
、大部分の気泡が連通したポリエチレン発泡体を製造す
ることの出来る方法を見出すに到つた。However, in this method, when polyethylene is foamed, most of the cells in the foam are independent, and they are completely impermeable to applications that require air permeability, such as filters. The inventor is
As a result of intensive research into ways to improve these shortcomings,
By specifying the melt index, mixing ratio, and extrusion temperature of low-density polyethylene and high-density polyethylene, we have discovered a method that can produce polyethylene foam in which most of the cells are connected.
すなわち本発明の要旨はメルトインデックス10以上の
高密度ポリエチレンとメルトインデックス1以下の低密
度ポリエチレンを、高密度ポリエチレンの含量が1.9
53.5p−O、、量%以上で、p−O、’量%以下(
ρは高密度ポリエチレンの密度)になるように混合した
混合樹脂に常圧下での沸点が100℃以下の揮発性有機
液体を高温高圧下で混合し、この混合物を低密度ポリエ
チレンの融点以上にして高密度ポリエチレンの融点より
も10℃低い温度以下の温度まで冷却し、しかるのち低
圧帯域に押出すことを特徴とするポリエチレン発泡体の
製造方法に存する。That is, the gist of the present invention is to combine high-density polyethylene with a melt index of 10 or more and low-density polyethylene with a melt index of 1 or less, with a content of high-density polyethylene of 1.9.
53.5 p-O,, amount % or more, p-O, 'amount % or less (
A volatile organic liquid with a boiling point of 100°C or less under normal pressure is mixed with a mixed resin so that ρ is the density of high-density polyethylene), and the mixture is heated to a temperature higher than the melting point of low-density polyethylene. The present invention relates to a method for producing polyethylene foam, which comprises cooling to a temperature 10° C. lower than the melting point of high-density polyethylene, and then extruding it into a low-pressure zone.
本発明に用いられる高密度ポリエチレン(以下HDPE
と云う)とはエチレン単独重合体又はエチレンと他の少
量なモノマーとの共重合体であつてJISに6760に
より測定した密度がO、940y/ cc以上のポリエ
チレンを指す。High-density polyethylene (hereinafter referred to as HDPE) used in the present invention
) refers to polyethylene that is an ethylene homopolymer or a copolymer of ethylene and a small amount of other monomers, and has a density of O, 940y/cc or more as measured according to JIS 6760.
そして本発明においては該HDPEのうちメルトインデ
ックス(以下■?1と云う)が10以上のものが選択的
に用いられる。又、本発明に用いられる低密度ポリエチ
レン(以下LDPEと云う)とはエチレン単独重合体又
はエチレンと他の少量なモノマーとの共重合体であつて
JISに6760により測定した密度が0.930ダ/
cc以下のポリエチレンを指す。In the present invention, among the HDPEs, those having a melt index (hereinafter referred to as ?1) of 10 or more are selectively used. Furthermore, the low-density polyethylene (hereinafter referred to as LDPE) used in the present invention is an ethylene homopolymer or a copolymer of ethylene and a small amount of other monomers, and has a density of 0.930 Da as measured by JIS 6760. /
Refers to polyethylene of cc or less.
そして本発明においては該LDPEのうちMIが1以下
のものが選択的に用いられる。又、本発明に用いられる
揮発性有機液体は常圧下での沸点が100℃以下の有機
液体であり、例えはプロパン、ブタン、ペンタン等の脂
肪族炭化水素、ジクロルジフルオロメタン、ジクロロテ
トラフルオロエタン、トリクロロモノフルオロメタン等
のハロゲン化炭化水素等があげられる。In the present invention, among the LDPEs, those having an MI of 1 or less are selectively used. Further, the volatile organic liquid used in the present invention is an organic liquid having a boiling point of 100°C or less under normal pressure, and examples thereof include aliphatic hydrocarbons such as propane, butane, and pentane, dichlorodifluoromethane, and dichlorotetrafluoroethane. , halogenated hydrocarbons such as trichloromonofluoromethane, and the like.
本発明方法により大部分の気泡が連通したポリエチレン
発泡体を製造するには、まずMIlO以上のI−[DP
EとMIl以下のLDPEとをHDPEの含量が丹′量
%以上でh評量%以下になるように混合した混合樹脂に
前記揮発性有機液体を高温高圧下で混合するのである。In order to produce a polyethylene foam in which most of the cells are connected by the method of the present invention, first, I-[DP
The volatile organic liquid is mixed under high temperature and high pressure into a mixed resin in which E and LDPE of less than MII are mixed such that the content of HDPE is greater than T% and less than H%.
上記の如く、本発明においてHDPE及びLDPE(7
)MIが特定されるのは、HDPE(7)MIが1昧満
てある場合やLDPEのMIが1よりも大きい場合には
、得られる発泡体の50%以上の気泡が連通する様に1
U)PEの混合比率を高めると気泡の不均一が生じ良好
な発泡体が得られないことが種々の実験の結果判明した
ことにもとづ゛いている。この理由は明らかでないが、
低圧帯域へ押出される際の樹脂温度では、HDPEは固
体状態であり、MIが1昧満のFIDPEでは気泡膜の
強度が大きすぎて揮発性液体の気化圧力では充分発泡で
きず高度に発泡した発泡体が得られず、又、MIが1を
越えたLDPEを用いると発泡の際、気泡膜中の樹脂組
成が不均一となり、微小なりラックを生じ、ここから発
泡剤が逸散し、高度に発泡した発泡体が得られないこと
によるものと考えられる。又、HDPEとLDPEの混
合比率については、HDPEが前記含量よりも少ない場
合は充分連通した気泡構造とならず、逆にHDPEが前
記含量よりも多い場合には、均一な気泡構造の発泡体が
得られない。なお本発明において揮発性有機液体を混合
する順序は混合樹脂に揮発性有機液体を混合する場合に
限られることはなく、HDPE(5LDPEのいずれか
一方に揮発性有機液体を混合しておき、これに他方を混
合する順序で行つてもよい。As mentioned above, in the present invention, HDPE and LDPE (7
) MI is specified because HDPE (7) When the MI is less than 1 or when the MI of LDPE is larger than 1, the MI is specified so that 50% or more of the cells in the obtained foam are connected.
U) This is based on the fact that it has been found through various experiments that increasing the mixing ratio of PE causes non-uniformity of cells and makes it impossible to obtain a good foam. The reason for this is not clear, but
At the resin temperature when extruded to the low pressure zone, HDPE is in a solid state, and in FIDPE with an MI of less than 1, the strength of the bubble membrane was too large to be sufficiently foamed under the vaporization pressure of a volatile liquid, resulting in a high degree of foaming. If a foam cannot be obtained, and if LDPE with an MI of more than 1 is used, the resin composition in the foam film will become non-uniform during foaming, resulting in minute racks from which the foaming agent will escape, resulting in high This is thought to be due to the fact that a foamed product cannot be obtained. Regarding the mixing ratio of HDPE and LDPE, if the content of HDPE is less than the above content, the cell structure will not be sufficiently open, whereas if the content of HDPE is more than the above content, the foam will not have a uniform cell structure. I can't get it. Note that in the present invention, the order in which the volatile organic liquid is mixed is not limited to the case where the volatile organic liquid is mixed with the mixed resin; This may be done in the order of mixing one with the other.
次に本発明では前記で混合したHDPE,LDPE及び
揮発性有機液体の混合物をLDPEの融点以上にしてH
DPEの融点よりも10℃低い温度以下の温度まで冷却
し、しかるのち低圧帯域に押出すのであり、かくするこ
とにより大部分の気泡が連続した気泡構造を有し、発泡
倍率の大きいポリエチレン発泡体が得られるのである。
しかして、本発明における混合物の冷却は上記の通りで
あるので、本発明に用いられるHDPEの融点とLDP
Eの融点との差は10℃よりも大きいことが必要であり
、上記の如き特定の温度まて混合物を冷却する理由は、
押出温度がLDPEの融点以下の場合は、該混合物の一
部又は全部が固化し、均一な発泡体とならないか又は押
出すことが不可能となり、又、該混合物がHDPEの融
点より10℃低い温度より高い温度て押出される場合に
は、押出されると同時に発泡剤が樹脂より逸散し、高度
に発泡した発泡体は得られないことが判明したことにも
とずく。Next, in the present invention, the mixture of HDPE, LDPE and volatile organic liquid mixed above is heated to a temperature higher than the melting point of LDPE.
It is cooled to a temperature 10°C lower than the melting point of DPE, and then extruded into a low-pressure zone, thereby creating a polyethylene foam with a cell structure in which most of the cells are continuous and a high expansion ratio. is obtained.
Since the cooling of the mixture in the present invention is as described above, the melting point of HDPE used in the present invention and the LDP
It is necessary that the difference between the melting point of E and the melting point of
If the extrusion temperature is below the melting point of LDPE, part or all of the mixture will solidify and will not form a uniform foam or will be impossible to extrude, and if the mixture is 10°C lower than the melting point of HDPE. This is based on the fact that it has been found that if extrusion is carried out at a temperature higher than this temperature, the blowing agent escapes from the resin at the same time as it is extruded, and a highly foamed foam cannot be obtained.
又、本発明を工業的に連続して実施する一つの方法とし
ては、押出機ホッパーからLDPEとHDPEの予備混
合物を供給し、HDPEの融点以上の温度に熔融混練し
、押出機バレルの途中に設けた注入孔より揮発性有機液
体を注入し、樹脂と混合し、用いたLDPEの融点以上
にしてHDPEの融点より10℃低い温度以下に冷却し
た后、所望の形状の口金から大気中に押出し発泡させる
方法がある。In addition, one method for carrying out the present invention industrially and continuously is to supply a premix of LDPE and HDPE from an extruder hopper, melt and knead it to a temperature higher than the melting point of HDPE, and then add it to the middle of the extruder barrel. A volatile organic liquid is injected through the injection hole provided, mixed with the resin, cooled to a temperature higher than the melting point of the LDPE used and 10°C lower than the melting point of HDPE, and then extruded into the atmosphere through a mouthpiece of the desired shape. There is a way to make it foam.
この際、通常用いられる気泡調整剤、着色剤、老化防止
剤、帯電防止剤等の添加剤を予め樹脂中に練込んでおく
か、あるいはホッパー又はバレルの途中から入れること
も可能である。本発明のポリエチレン発泡体の製造方法
は上述の通りの方法であるので、気泡の大部分が連通し
た連続気泡を有し、発泡倍率も高い良質なポリエチレン
発泡体を簡単に得ることが出来るのであり、得られた発
泡体は連続気泡が要求されるフィルター等の種々の用途
に使用され得る。At this time, commonly used additives such as a bubble control agent, colorant, antiaging agent, and antistatic agent may be kneaded into the resin in advance, or they may be added from the middle of the hopper or barrel. Since the method for manufacturing the polyethylene foam of the present invention is as described above, it is possible to easily obtain a high-quality polyethylene foam that has a majority of open cells and has a high expansion ratio. The resulting foam can be used in various applications such as filters where open cells are required.
以下本発明の実施例について説明する。Examples of the present invention will be described below.
実施例1及び比較例1
M113、密度0.965y/Cc融点135℃のE)
PEとMlO.3、密度0.923y/Ccl融点11
0℃のLDPEを第1表の割合で混合したものを、口径
50Tn1L/D=30の押出機に供給し、10kg/
Hの割合で押出し、バレルの途中に設けた発泡剤注入孔
よりジクロロテトラフルオロエタンを2.5k9/Hの
割合で注入し樹脂と混練し、樹脂温度を第1表に示され
る温度まで下げて調節した后、口径4T1mの円孔ノズ
ルから大気中に押出した。Example 1 and Comparative Example 1 M113, density 0.965y/Cc melting point 135°C E)
PE and MIO. 3. Density 0.923y/Ccl melting point 11
A mixture of LDPE at 0°C in the proportions shown in Table 1 was supplied to an extruder with a diameter of 50Tn1L/D=30, and 10kg/
Dichlorotetrafluoroethane was injected at a rate of 2.5k9/H through a blowing agent injection hole provided in the middle of the barrel, kneaded with the resin, and the resin temperature was lowered to the temperature shown in Table 1. After adjustment, it was extruded into the atmosphere through a circular hole nozzle with a diameter of 4T1 m.
気泡調整剤としてタルク微粉末を樹脂1(4)重量部に
対して0.5重量部の割合で樹脂に混合して用いた。得
られた発泡体を空気比較式比重計で、その連続気泡率を
測定した。結果は第1表の通りである。実施例2及び比
較例2
M112、密度0.94y/Ccl融点124℃のHD
PEとMlO.3、密度0.923y/Ccl融点11
0℃のLDPEを第2表の割合で混合したものを実施例
1で用いた押出機にて10kg/Hの割合で押出し、発
泡剤注入孔よりジクロロジフルオロメタンを2k9/H
の割合で注入し樹脂と混練し、樹脂温度を下げて112
℃に調節した后、口径47WLの円孔ノズルから大気中
に押出した。Fine talc powder was used as a foam regulator by mixing with the resin at a ratio of 0.5 parts by weight per 1 (4) parts by weight of the resin. The open cell ratio of the obtained foam was measured using an air comparison hydrometer. The results are shown in Table 1. Example 2 and Comparative Example 2 M112, HD with density 0.94y/Ccl melting point 124°C
PE and MIO. 3. Density 0.923y/Ccl melting point 11
A mixture of LDPE at 0°C in the proportions shown in Table 2 was extruded at a rate of 10kg/H using the extruder used in Example 1, and dichlorodifluoromethane was added at 2k9/H through the blowing agent injection hole.
Inject at a ratio of 112, mix with resin, lower the resin temperature
After adjusting the temperature to .degree. C., it was extruded into the atmosphere through a circular hole nozzle with a diameter of 47WL.
気泡調整剤を実施例1と同様に用いた。得られた結果は
第2表の通りてある。比較例3M15、密度0.957
y/Ccl融点128゜C(7)HDPE4O重量部と
MlO.く密度0.923y/Ccl融点110℃のL
DPE6O重量部を実施例1と同じ押出機を用いて、1
0k9/(Iの割合て押出し、発泡剤注入孔よりジクロ
ロテトラフルオロエタンを2.5kg/Hの割合で注入
し、樹脂と発泡剤を混練したのち混合物を115℃まて
冷却して、口径477!77!の円孔ノズルから大気中
へ押し出した。A cell control agent was used in the same manner as in Example 1. The results obtained are shown in Table 2. Comparative example 3M15, density 0.957
y/Ccl melting point 128°C (7) parts by weight of HDPE4O and MIO. L with density 0.923y/Ccl melting point 110℃
Using the same extruder as in Example 1, 1 part by weight of DPE6O was added.
Extrude at a rate of 0k9/(I, inject dichlorotetrafluoroethane at a rate of 2.5kg/H from the blowing agent injection hole, knead the resin and blowing agent, cool the mixture to 115°C, and make a caliber of 477 It was extruded into the atmosphere through the circular hole nozzle of !77!.
Claims (1)
とメルトインデックス1以下の低密度ポリエチレンを、
高密度ポリエチレンの含量が1.95/ρ−0.9重量
%以上で3.5/ρ−0.9重量%以下(ρは高密度ポ
リエチレンの密度)になるように混合した混合樹脂に常
圧下での沸点が100℃以下の揮発性有機液体を高温高
圧下で混合し、この混合物を低密度ポリエチレンの融点
以上にして高密度ポリエチレンの融点よりも10℃低い
温度以下の温度まで冷却し、しかるのち低圧帯域に押出
すことを特徴とするポリエチレン発泡体の製造方法。1 High-density polyethylene with a melt index of 10 or more and low-density polyethylene with a melt index of 1 or less,
Always use a mixed resin mixed so that the content of high-density polyethylene is 1.95/ρ-0.9% by weight or more and 3.5/ρ-0.9% by weight or less (ρ is the density of high-density polyethylene). Volatile organic liquids with a boiling point under pressure of 100°C or less are mixed under high temperature and high pressure, and the mixture is cooled to a temperature equal to or higher than the melting point of low-density polyethylene and 10°C lower than the melting point of high-density polyethylene, A method for producing polyethylene foam, characterized in that it is then extruded into a low pressure zone.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54104626A JPS6055290B2 (en) | 1979-08-16 | 1979-08-16 | Method for manufacturing polyethylene foam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54104626A JPS6055290B2 (en) | 1979-08-16 | 1979-08-16 | Method for manufacturing polyethylene foam |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5628837A JPS5628837A (en) | 1981-03-23 |
| JPS6055290B2 true JPS6055290B2 (en) | 1985-12-04 |
Family
ID=14385642
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54104626A Expired JPS6055290B2 (en) | 1979-08-16 | 1979-08-16 | Method for manufacturing polyethylene foam |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6055290B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997018260A1 (en) * | 1995-11-15 | 1997-05-22 | Asahi Kasei Kogyo Kabushiki Kaisha | Pre-expanded polyethylene beads and process for the production thereof |
| US6541533B2 (en) | 2001-01-10 | 2003-04-01 | Jsp Corporation | Extruded polyolefin resin foam |
| JP5005173B2 (en) * | 2005-02-08 | 2012-08-22 | ダイセルノバフォーム株式会社 | Resin composition for foam and foam using the same |
-
1979
- 1979-08-16 JP JP54104626A patent/JPS6055290B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5628837A (en) | 1981-03-23 |
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