JPS5968215A - Manufacture of polyolefin resin molded body foamed in mold - Google Patents
Manufacture of polyolefin resin molded body foamed in moldInfo
- Publication number
- JPS5968215A JPS5968215A JP57179374A JP17937482A JPS5968215A JP S5968215 A JPS5968215 A JP S5968215A JP 57179374 A JP57179374 A JP 57179374A JP 17937482 A JP17937482 A JP 17937482A JP S5968215 A JPS5968215 A JP S5968215A
- Authority
- JP
- Japan
- Prior art keywords
- particles
- expanded particles
- mold
- foamed
- polyolefin 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.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3461—Making or treating expandable particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/36—Feeding the material to be shaped
- B29C44/38—Feeding the material to be shaped into a closed space, i.e. to make articles of definite length
- B29C44/44—Feeding the material to be shaped into a closed space, i.e. to make articles of definite length in solid form
- B29C44/445—Feeding the material to be shaped into a closed space, i.e. to make articles of definite length in solid form in the form of expandable granules, particles or beads
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3415—Heating or cooling
- B29C44/3426—Heating by introducing steam in the mould
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
Landscapes
- Molding Of Porous Articles (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
【発明の詳細な説明】 方法に関する。[Detailed description of the invention] Regarding the method.
従来より合成樹脂発泡成型体、例えばポリスチレン発泡
成型体、ポリエチレン発泡成型体等が包装材、緩衝材、
浮揚材等多方面に用いられている。Conventionally, synthetic resin foam moldings, such as polystyrene foam moldings and polyethylene foam moldings, have been used as packaging materials, cushioning materials,
It is used in many ways such as flotation materials.
これらの発泡成型体は押出成熟法または予備発泡粒子を
用いる所謂ビーズ成型法により製造されている。ここで
ビーズ成型法により発泡成型体を得る場合には同一の樹
脂より予備発泡粒子を製造し、その予備発泡粒子を用い
て発泡成型体を製造しているが、粒子が適正な軟化状態
でないと得られる発泡成型体の外観、融着性等が損なわ
れるので成型温度を制御する必要がある。しかし々がら
、ポリオレフィン樹脂は適正な成型温度の幅が非常に狭
く、その条件の設定を厳格に行なう必要がある等、成型
性の面で未だ改良の余地を残しているものである。These foam molded bodies are manufactured by an extrusion maturation method or a so-called bead molding method using pre-expanded particles. When obtaining a foam molded product using the bead molding method, pre-expanded particles are produced from the same resin, and the pre-expanded particles are used to produce a foam molded product, but if the particles are not in an appropriate softened state. It is necessary to control the molding temperature since the appearance, fusion properties, etc. of the resulting foam molded product are impaired. However, polyolefin resins have a very narrow range of suitable molding temperatures, and the conditions must be set strictly, so there is still room for improvement in terms of moldability.
とを目的とするものであって、本発明者らは上記を成型
用型に混合充填した後加熱、発泡することにより成型性
、外観、融着性が良好な発泡成型体が広汎な温度条件下
で得られることを見出すと共にその製造方法の開発に成
功し、本発明を完成するに至った。The present inventors mixed and filled the above ingredients into a mold, then heated and foamed them, thereby producing a foam molded product with good moldability, appearance, and fusion properties under a wide range of temperature conditions. The present inventors have discovered that the following can be obtained and succeeded in developing a method for producing the same, thereby completing the present invention.
すなわち、本発明は融点が異なる29以上の同種のポリ
オレフィン樹脂予備発泡粒子を成型用型とするものであ
る。That is, the present invention uses pre-expanded polyolefin resin particles of the same type having different melting points of 29 or more as a mold.
本発明において、ポリオレフィン樹脂予備発泡粒子の材
質としては、例えば低密度ポリエチレン(以下、LDP
Eと略称する。)、直鎖低密度ポリエチレン(以下、L
LDPEと略称する。)、高密度ポリエチレン(以下、
HDPEと略称する0)等のポリエチレン、ポリプロピ
レン単独重合体、゛エチレンープロピレンランダム共重
合体、エチレン−プロピレンブロック共重合体等のポリ
プロピレン系樹脂、エチレン−α−オレフィン共重合体
、プロピレン−α−オレフィン共重合体、エチレン−ブ
タジェン共重合体、ポリブテン等が挙げられる。尚、上
記ポリオレフィン樹脂は架橋したもの無架橋のものいず
れも用いることができる。In the present invention, the material of the polyolefin resin pre-expanded particles is, for example, low density polyethylene (hereinafter referred to as LDP).
It is abbreviated as E. ), linear low-density polyethylene (hereinafter referred to as L
It is abbreviated as LDPE. ), high-density polyethylene (hereinafter referred to as
Polyethylene such as HDPE (0), polypropylene homopolymer, polypropylene resin such as ethylene-propylene random copolymer, ethylene-propylene block copolymer, ethylene-α-olefin copolymer, propylene-α- Examples include olefin copolymers, ethylene-butadiene copolymers, polybutenes, and the like. The above polyolefin resin may be either crosslinked or non-crosslinked.
本発明に用いられるポリオレフィン樹脂予備発泡粒子は
例えば次のような予備発泡方法によって製造することが
できる。すなわち、密閉容器内でポリオレフィン樹脂粒
子内に揮発性発泡剤を含有させる工程、孝排溶壜哨千樹
脂粒子を分散媒に分散させ所定温度に加熱する工程、お
よび容器の一端を開放し、上記粒子と分散媒を同時に容
器内よりも低圧の雰囲気に放出する工程よりなる予備発
泡方法によって製造することができる。The pre-expanded polyolefin resin particles used in the present invention can be produced, for example, by the following pre-expanding method. That is, a step of incorporating a volatile blowing agent into polyolefin resin particles in a closed container, a step of dispersing the resin particles in a dispersion medium and heating them to a predetermined temperature, and a step of opening one end of the container and performing the above-mentioned steps. It can be produced by a pre-foaming method comprising a step of simultaneously releasing the particles and the dispersion medium into an atmosphere at a lower pressure than in the container.
上記方法に用いる揮発性発泡剤としては、例えハフロパ
ン、′ブタン、ペンタン、ヘキサノ、ヘプタン等で例示
される脂肪族炭化水素類、シクロブタン、シクロペンタ
ン等で例示される環式脂肪族炭化水素類、およびトリク
ロロフロロメタン、ジクロロジフロロメタン、ジクロロ
テトラフロロエタン、メチルフクロライド、エチルクロ
ライド、メチレンクロライド等で例示されるハロゲン化
炭化水素類等が使用される。この発泡剤の添加量は通常
樹脂粒子ioo重量部に対し5〜40重量部重量部−ら
れる。Volatile blowing agents used in the above method include aliphatic hydrocarbons such as haflopane, 'butane, pentane, hexano, heptane, etc., cyclic aliphatic hydrocarbons such as cyclobutane, cyclopentane, etc. Also used are halogenated hydrocarbons such as trichlorofluoromethane, dichlorodifluoromethane, dichlorotetrafluoroethane, methylfluorochloride, ethyl chloride, and methylene chloride. The amount of the blowing agent added is usually 5 to 40 parts by weight per 100 parts by weight of the resin particles.
上記方法では樹脂粒子と揮発性発泡剤を別々に蹟
或いは揮発性発泡剤を樹脂粒子に含有させハ雰散媒に分
散させるが、このとき要すれば分散剤、例えば微粒状の
酸化アルミニウムおよび酸化チタン、塩基性炭酸マグネ
シウム、塩基性炭酸亜鉛、炭酸カルシウム等を用いるこ
とができる。この分散剤の添加量は樹脂粒子100重量
部に対し0,01〜10重量部である。また分散媒は樹
脂粒子を溶解させない溶媒であればよく、例えば水、エ
チレングリコール、グリセリン、メタノール、エタノー
ル等のうちの1種またはそれらの2種以上の混合物が例
示されるが、通常は水が好ましい。In the above method, the resin particles and the volatile blowing agent are separated separately or the volatile blowing agent is contained in the resin particles and dispersed in the atmospheric dispersion medium. Titanium, basic magnesium carbonate, basic zinc carbonate, calcium carbonate, etc. can be used. The amount of the dispersant added is 0.01 to 10 parts by weight per 100 parts by weight of the resin particles. The dispersion medium may be any solvent that does not dissolve the resin particles, and examples include water, ethylene glycol, glycerin, methanol, ethanol, etc., or a mixture of two or more thereof, but water is usually used. preferable.
また上記の方法では容器の一端を開放して樹脂粒子と分
散媒とを同時に容器内よりも低圧の雰囲気に放出するが
、このときの容器内の温度は90〜170℃が好ましく
、圧力は揮発性発泡剤の蒸気圧以上または未満のいずれ
でもよく、放出する雰囲気は通常常圧の雰囲気が選ばれ
る。In addition, in the above method, one end of the container is opened and the resin particles and dispersion medium are simultaneously released into an atmosphere with a lower pressure than the inside of the container. At this time, the temperature inside the container is preferably 90 to 170°C, and the pressure is set to evaporate. The pressure may be higher than or lower than the vapor pressure of the foaming agent, and the atmosphere to be discharged is normally selected to be at normal pressure.
このようにして得られるポリオレフィン樹脂予備発泡粒
子は揮発性発泡剤の量、温度、圧力等によっても異なる
が、通常5〜50倍の見掛は発泡倍率を有する。また得
られた予備発泡粒子に揮発性発泡剤または後述する無機
ガス等により内圧を付与した後加熱して見掛は発泡倍率
20〜150倍の予備発泡粒子を得ることもできる。The polyolefin resin pre-expanded particles thus obtained usually have an apparent expansion ratio of 5 to 50 times, although this varies depending on the amount of volatile blowing agent, temperature, pressure, etc. Further, it is also possible to obtain pre-expanded particles having an apparent expansion ratio of 20 to 150 times by applying internal pressure to the obtained pre-expanded particles using a volatile blowing agent or an inorganic gas as described below and then heating them.
得られた予備発泡粒子は要すれば常温常圧下熟揮°発性
発泡剤との混合ガスにより加圧熟成して粒子内に内圧を
付与する。無機ガスとしては、例えば空気、窒素、アル
ゴン、ヘリウノ、等が用いられる。The obtained pre-expanded particles are aged under normal temperature and pressure, if necessary, with a mixed gas with a volatile foaming agent to impart internal pressure to the inside of the particles. As the inorganic gas, for example, air, nitrogen, argon, helium, etc. are used.
本発明において、ポリオレフィン樹脂予備発泡粒子は融
点の異なる粒子を混合するが、融点の差は通常2〜35
℃であるが、好ましくは3〜20℃、さらに好ましくは
5〜15℃である。また粒子の混合は同種類のもの、例
えばポリエチレン系樹脂−ポリエチレン系樹脂、ポリプ
ロピレン系樹脂−ポリプロピレン系樹脂によシ行なう必
要がある。異種のものの場合には樹脂間の親和性の問題
等により融着の良好な発泡成型品を得ることが困難であ
る。In the present invention, the polyolefin resin pre-expanded particles are mixed with particles having different melting points, and the difference in melting point is usually 2 to 35.
℃, preferably 3 to 20℃, more preferably 5 to 15℃. It is also necessary to mix particles of the same type, for example, polyethylene resin-polyethylene resin, polypropylene resin-polypropylene resin. In the case of different types of resins, it is difficult to obtain a foam molded product with good fusion bonding due to affinity problems between the resins.
上記の予備発泡粒子を成型用型内に混合充填するに当っ
て、融点が高い粒子Aと低い粒子Bとの混合比A二Bは
特に限定されないが、1:5〜5:1の範囲が好ましい
。また予備発泡粒子の混合充填は融点が同じ粒子が集合
せず分散状態で行なうことが好ましい。When mixing and filling the above pre-expanded particles into a mold, the mixing ratio A to B of particles A with a high melting point and particles B with a low melting point is not particularly limited, but is preferably in the range of 1:5 to 5:1. preferable. In addition, it is preferable that the pre-expanded particles be mixed and filled in a dispersed state without particles having the same melting point being aggregated.
上記予備発泡粒子の融点の一例を挙げると下記の如くで
ある。An example of the melting point of the pre-expanded particles is as follows.
基 材 樹 脂 融 点
(OLDPK 98〜110
L L D P g 115〜130HDPE
130〜138
また予備発泡粒子は3種類以上混合することもでき、そ
の場合には融点の差がより太きいものも成型できる効果
がある。Base material resin melting point (OLDPK 98~110 LLDP g 115~130HDPE
130-138 Moreover, three or more types of pre-expanded particles can be mixed, and in this case, there is an effect that particles having a larger difference in melting point can also be molded.
本発明において成型用型としては、型面に加熱媒体が通
過する小孔を有する通常の金型を用いることができ、ま
た加熱媒体としては0.8〜5.Oq/ ca (G)
の水蒸気を用いることができる。これにより予備発泡粒
子を加熱発泡して型通りのの発泡成成型体は例えば、包
装材、緩衝材、保温材、断熱材、建築資材、車輌部材、
浮揚材、食品容器等に用いることができる。In the present invention, as the mold for molding, an ordinary mold having small holes on the mold surface through which a heating medium passes can be used, and the heating medium is 0.8 to 5. Oq/ca (G)
water vapor can be used. As a result, the pre-expanded particles are heated and foamed to produce a foam molded product that can be used, for example, in packaging materials, cushioning materials, heat insulating materials, insulation materials, building materials, vehicle components, etc.
It can be used for flotation materials, food containers, etc.
以上説明したように、本発明によれば、同種の融点が異
なる2種類以上のポリオレフィン樹脂予備発泡粒子を成
型用型に混合、充填して加熱、発泡するので成型性が良
好なものであり、かつ得られる発泡成型体は良好な外観
、融着性等を有するものでろる。As explained above, according to the present invention, two or more types of polyolefin resin pre-expanded particles of the same type with different melting points are mixed and filled into a mold, heated and foamed, so that moldability is good. The foamed molded product obtained also has good appearance, fusion properties, etc.
以下、調製例、実施例および比較例を掲げて本発明をさ
らに詳細に説明する。Hereinafter, the present invention will be explained in further detail with reference to Preparation Examples, Examples, and Comparative Examples.
調製例A−に
第1表に示す融点を有する基材樹脂粒子100重量部、
第1表に示す種類および使用量の揮発性発泡剤、分散剤
および分散媒をオートクレーブに入れ、攪拌下100〜
165℃の温度に加熱し、オートクレーブの一端を開放
して樹脂粒子と水とを同時に大気下に放出し、第1表に
示す発泡倍率を有する予備発泡粒子を得だ。In Preparation Example A-, 100 parts by weight of base resin particles having the melting point shown in Table 1,
Volatile blowing agents, dispersants, and dispersion media of the types and amounts shown in Table 1 were placed in an autoclave, and the
The autoclave was heated to a temperature of 165°C, one end of the autoclave was opened, and the resin particles and water were simultaneously discharged into the atmosphere to obtain pre-expanded particles having the expansion ratio shown in Table 1.
実施例1〜9 および比較例1〜11
調製例により得られた予備発泡粒子(A−K)を常温常
圧下48時間放置した後、該粒子に空気により(18K
P/c4(G)の内圧を付与した後、長さ300朋、幅
300mw厚さ30+gの金型に、第2表に示す如く同
種の融点が異なる粒子を混合、充填し、0.8〜4KP
/JG)の水蒸気で加熱発泡させて発泡成成型性、外観
、融着性を測定した。結果を第2表に示す。Examples 1 to 9 and Comparative Examples 1 to 11 After leaving the pre-expanded particles (A-K) obtained in the Preparation Example at room temperature and normal pressure for 48 hours, the particles were heated with air (18K).
After applying an internal pressure of P/c4 (G), particles of the same kind with different melting points as shown in Table 2 are mixed and filled into a mold with a length of 300 mm, a width of 300 mw, and a thickness of 30+ g. 4KP
/JG) was heated and foamed with water vapor, and the foam moldability, appearance, and fusion properties were measured. The results are shown in Table 2.
第 2 表
※1−成型性は成型可能な蒸気圧の幅により次の如く判
定した。Table 2 *1 - Moldability was determined as follows based on the range of moldable vapor pressure.
0、4 KP/ cイ以上 00.2〜0.4
KP/c4%J ”0、2 Ky / cA
未満 ×※2−外観は成型体の表面状態により
下記の如く判定した。0,4 KP/c or more 00.2~0.4
KP/c4%J ”0,2 Ky/cA
Less than × *2 - Appearance was determined as follows based on the surface condition of the molded product.
平 滑 ○若干の凹凸
△
凹凸著しい ×
※3−融着性は発泡成型体を折り曲げたときの状態によ
り下記の如く判定した。Smooth ○ Some unevenness
△ Significant unevenness × *3 - Fusion adhesion was determined as follows based on the state of the foamed molded product when it was folded.
融着している ○ 部分的に割れる △Fused ○ Partially cracked △
Claims (1)
の製造方法。A method for producing two or more polyolefin foam molded products of the same type having different melting points.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57179374A JPS5968215A (en) | 1982-10-13 | 1982-10-13 | Manufacture of polyolefin resin molded body foamed in mold |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57179374A JPS5968215A (en) | 1982-10-13 | 1982-10-13 | Manufacture of polyolefin resin molded body foamed in mold |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5968215A true JPS5968215A (en) | 1984-04-18 |
JPS6244778B2 JPS6244778B2 (en) | 1987-09-22 |
Family
ID=16064732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57179374A Granted JPS5968215A (en) | 1982-10-13 | 1982-10-13 | Manufacture of polyolefin resin molded body foamed in mold |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5968215A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0279455A2 (en) * | 1987-02-20 | 1988-08-24 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for production of expansion-molded articles of linear low density polyethylene resins |
US5128183A (en) * | 1990-08-01 | 1992-07-07 | Borden, Inc. | Modified polyolefin film with stable twist retention, dead fold properties and barrier characteristics |
US6087446A (en) * | 1996-03-20 | 2000-07-11 | Hercules Incorporated | Masterbatch formulations for polyolefin applications |
US6255395B1 (en) | 1999-03-22 | 2001-07-03 | Hercules Incorporated | Masterbatches having high levels of resin |
WO2018105394A1 (en) * | 2016-12-07 | 2018-06-14 | 三菱電機株式会社 | Foamed heat-insulating material production method and foamed heat-insulating material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5151020B2 (en) * | 2005-02-01 | 2013-02-27 | 株式会社カネカ | Thermoplastic resin in-mold foam molding |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5214739A (en) * | 1975-07-21 | 1977-02-03 | Teijin Hercules Kk | Process for recovery of terephthalic acid |
-
1982
- 1982-10-13 JP JP57179374A patent/JPS5968215A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5214739A (en) * | 1975-07-21 | 1977-02-03 | Teijin Hercules Kk | Process for recovery of terephthalic acid |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0279455A2 (en) * | 1987-02-20 | 1988-08-24 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for production of expansion-molded articles of linear low density polyethylene resins |
US5128183A (en) * | 1990-08-01 | 1992-07-07 | Borden, Inc. | Modified polyolefin film with stable twist retention, dead fold properties and barrier characteristics |
US6087446A (en) * | 1996-03-20 | 2000-07-11 | Hercules Incorporated | Masterbatch formulations for polyolefin applications |
US6281290B1 (en) | 1996-03-20 | 2001-08-28 | Eastman Chemical Company | Compositions, processes for making, and articles of polyolefins, high density polyethylene and hydrocarbon resin |
US6255395B1 (en) | 1999-03-22 | 2001-07-03 | Hercules Incorporated | Masterbatches having high levels of resin |
WO2018105394A1 (en) * | 2016-12-07 | 2018-06-14 | 三菱電機株式会社 | Foamed heat-insulating material production method and foamed heat-insulating material |
Also Published As
Publication number | Publication date |
---|---|
JPS6244778B2 (en) | 1987-09-22 |
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