JPS5852328A - Production of polypropylene resin foam - Google Patents
Production of polypropylene resin foamInfo
- Publication number
- JPS5852328A JPS5852328A JP56149806A JP14980681A JPS5852328A JP S5852328 A JPS5852328 A JP S5852328A JP 56149806 A JP56149806 A JP 56149806A JP 14980681 A JP14980681 A JP 14980681A JP S5852328 A JPS5852328 A JP S5852328A
- Authority
- JP
- Japan
- Prior art keywords
- particles
- expanded
- expanded particles
- polypropylene resin
- internal pressure
- 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 description 18
- 239000011347 resin Substances 0.000 title claims description 18
- -1 polypropylene Polymers 0.000 title claims description 13
- 239000004743 Polypropylene Substances 0.000 title claims description 12
- 229920001155 polypropylene Polymers 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000006260 foam Substances 0.000 title description 7
- 239000002245 particle Substances 0.000 claims description 62
- 239000002253 acid Substances 0.000 claims description 3
- 239000004604 Blowing Agent Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000002612 dispersion medium Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 230000004927 fusion Effects 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 238000005187 foaming Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 229920013716 polyethylene resin Polymers 0.000 description 2
- 230000005070 ripening Effects 0.000 description 2
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 1
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 229920005676 ethylene-propylene block copolymer Polymers 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 229910001872 inorganic gas Inorganic materials 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229940073584 methylene chloride Drugs 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明はポリプロピレン系樹脂発泡成型体の製造方法に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a polypropylene resin foam molded article.
従来、ポリオレフィン系樹脂2例えばポリエチレン系樹
脂発泡成型体を得る方法として、架橋ポリエチレン樹脂
粒子より得られた予備発泡粒子を用いる方法が知られて
いる。この方法で社予備発泡粒子の発泡倍率に関係なく
予備発泡粒子に一定の内圧を付与し九後、成型を行なっ
て発泡成型体を得ているものである。BACKGROUND ART Conventionally, as a method for obtaining a polyolefin resin 2 such as a polyethylene resin foam molded article, a method using pre-expanded particles obtained from crosslinked polyethylene resin particles has been known. In this method, a constant internal pressure is applied to the pre-expanded particles regardless of the expansion ratio of the pre-expanded particles, and then the particles are molded to obtain a foamed molded article.
一方、ポリプロピレン系樹脂について妹、それ自身の性
質として機械的強度、耐熱性が大きく。On the other hand, regarding polypropylene resin, it has great mechanical strength and heat resistance as its own properties.
耐薬品性、耐油性、緩価性、低温特性が優れている等の
優れた性質を有することからその発泡成型体の開発が望
まれていたが、押出成形による板状またはシート状の簡
単な形状のものは製造されているものの複維な形状のも
の社得ることができなかった。しかしながら2本出願人
はさらに研究をすすめ九結果、予備発泡粒子を用いて成
型体を得る。所謂ビーズ成型法の開発に成功し、その予
備発泡粒子の製造法およびそれを用いる成型体の製造方
法を先に提案した。そこで、さらに改棗され良成型体の
製造方法を得るべく検討した結果、ポリプロピレン系樹
脂予備発泡粒子においては、ポリエチレン樹脂の場合の
ように発泡倍率に関係なく一定の粒子内圧を付与して成
型を行なったのでは一般に融着状態が良好で且つ収縮の
ない良好な成型体を得ることが困難であることが判明し
た。Due to its excellent properties such as chemical resistance, oil resistance, low temperature properties, and low-temperature properties, it has been desired to develop a foam molded product. Although products in the shape of fibers are manufactured, it was not possible to obtain products in the shape of multiple fibers. However, the applicant conducted further research and obtained a molded article using pre-expanded particles. We have successfully developed a so-called bead molding method, and have previously proposed a method for manufacturing pre-expanded particles and a method for manufacturing molded objects using it. Therefore, as a result of further investigation to obtain a method for manufacturing improved molded bodies, we found that polypropylene resin pre-expanded particles can be molded by applying a constant internal pressure to the particles regardless of the expansion ratio, as in the case of polyethylene resin. However, it has been found that it is generally difficult to obtain a molded body with a good welding state and no shrinkage.
本発明は優れた性質を有する嵐好なボリプロビレン系樹
脂発泡成型体の製造方法を提供することを目的とするも
のであって1本発明者らは上記目的を達成するために予
備発泡粒子の内圧と発泡倍率との関係に着目して鋭意研
究した結果、優れた性質を有する巌好な発泡成型体の製
造方法の確立に成功し1本発明を完成するに至った。An object of the present invention is to provide a method for producing a polypropylene resin foam molded product having excellent properties and good properties, and in order to achieve the above object, the present inventors have developed an internal pressure of pre-expanded particles. As a result of intensive research focusing on the relationship between foaming ratio and foaming ratio, we succeeded in establishing a method for producing a suitable foamed molded product with excellent properties, and completed the present invention.
すなわち2本発明は、予備発泡粒子の内圧と見掛は発泡
倍率が式: 0.01 m4F!0.5 xi (式中
。In other words, in the present invention, the internal pressure of pre-expanded particles and the apparent expansion ratio are expressed by the formula: 0.01 m4F! 0.5 xi (in the formula.
Pは予備発泡粒子の内圧(ゆ/j(G)) −vn F
i予備発泡粒子の見掛は発泡倍率をそれぞれ示す。)で
表わされる関係を有するポリプロピレン系樹脂予備発泡
粒子を用いて成型することを特徴とするポリプロピレン
系樹脂発泡成型体の製造方法を要旨とするものである。P is the internal pressure of pre-expanded particles (Y/j (G)) -vn F
i The appearance of pre-expanded particles indicates the expansion ratio. The gist of the present invention is a method for manufacturing a polypropylene resin foam molded article, which is characterized by molding using pre-expanded polypropylene resin particles having the relationship expressed by the following.
本発明に用いられるポリプロピレン系樹脂予備発泡粒子
の基材樹脂としては、プロピレン単独重合体、エチレン
−プロピレンランダム共重合体。The base resin of the pre-expanded polypropylene resin particles used in the present invention includes a propylene homopolymer and an ethylene-propylene random copolymer.
エチレン−プロピレンブロック共重合体勢が挙げられ、
これらは架橋したものまた祉無架橋のものいずれでもよ
いが特に無架橋のものに有益である。Examples include ethylene-propylene block copolymer configuration,
These may be either crosslinked or non-crosslinked, but non-crosslinked ones are particularly useful.
本発明に用いられるポリプロピレン系樹脂予備発泡粒子
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2重合体粒子内に揮発性発泡剤を含
有させる工程、 1!F閉容器内で重合体粒子を分散媒
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
の雰囲気下に放出する工程よりなる予備発泡方法によっ
て製造することがてきる。The pre-expanded polypropylene 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 the bipolymer particles, 1! F consists of a step of dispersing polymer particles in a dispersion medium and heating it to a predetermined temperature in a closed container, and a step of opening one end of the container and simultaneously releasing the particles and the dispersion medium into an atmosphere at a lower pressure than inside the container. It can be produced by a pre-foaming method.
この方法に用いる揮発性発泡剤としては2例えばプロパ
ン、ブタン、ペンタン、ヘキサン、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7
等で例示される狽式脂訪族炭化水素類及びトリクロロフ
ロロメタン、ジクロロシフ0ロメタン、ジクロロシフ0
ロメタン。Volatile blowing agents used in this method include 2, aliphatic hydrocarbons such as propane, butane, pentane, hexane, heptane, etc., cyclobutane, cyclopenta7, etc.
etc., and trichlorofluoromethane, dichlorosifu 0 romethane, dichlorosifu 0 romethane, etc.
Lomethane.
メチルクロライド、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ll#に@定されないが2通
常重合体粒子100重量部に対し5〜30重量部1!度
用いられる。揮発性発泡剤を重合体粒子に含有させる時
期は特に限定されない。Halogenated hydrocarbons such as methyl chloride, ethyl chloride, methylene chloride, etc. are used. The amount of this blowing agent added is not determined by ll#, but is usually 5 to 30 parts by weight per 100 parts by weight of the polymer particles. Used frequently. There is no particular limitation on the timing of incorporating the volatile blowing agent into the polymer particles.
従って予め重合体粒子に発泡剤を含有させておき。Therefore, the polymer particles should contain a foaming agent in advance.
この発泡剤を含有した重合体粒子を密閉容器内に入れて
該密閉容器内で分散媒に分散させてもよく。The polymer particles containing the blowing agent may be placed in a closed container and dispersed in a dispersion medium within the closed container.
或いは重合体粒子と発泡剤を密閉容器内に入れて骸密閉
容器内でそれらを分散媒に分散させつつ重合体粒子に発
泡剤を含有させてもよい。また密閉II容器内前記粒子
を所定温度に加熱する過1!1において、或いは加熱し
た後Ksi−いて発泡剤を密閉容器内に入れて前記粒子
と発泡剤を分散させつつ前記粒子に発泡剤を含有させて
もよい。冑、*記粒子に発泡剤を含有させるときの温度
も任意であり。Alternatively, the polymer particles and the blowing agent may be placed in a closed container and dispersed in a dispersion medium in the closed container so that the polymer particles contain the blowing agent. In addition, in step 1.1 of heating the particles to a predetermined temperature in a sealed II container, or after heating, a blowing agent is placed in the airtight container and the blowing agent is applied to the particles while dispersing the particles and the blowing agent. It may be included. The temperature at which the blowing agent is incorporated into the particles marked with * is also arbitrary.
養に限定されない。It is not limited to nutrition.
この方法では1重合体粒子と揮発性発泡剤を別々に威い
祉揮発性発泡剤を重合体粒子に含有させた後2分散媒に
分散させるが、このとき要すれば分散剤1例えば微粒状
の酸化アルミニラムシよび酸化チタン、塩基性員酸!グ
ネシウム、塩基性巌酸亜鉛、縦酸カルシウム等を用いる
ことができる。In this method, 1 polymer particles and a volatile blowing agent are separately dispersed, and the volatile blowing agent is incorporated into the polymer particles, and then dispersed in 2 dispersion media. Aluminum oxide and titanium oxide, basic acid! Gnesium, basic zinc sulfate, calcium sulfate, etc. can be used.
この分散剤の添加量は通常1重合体粒子100重量11
に対し0.01〜10重量部である。tた1分散媒は重
合体粒子を溶解させない溶媒であればよく2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
ノール郷のうちの1種又はそれらの2種以上の混合物が
例示されるが通常は水が好ましい。The amount of this dispersant added is usually 1 polymer particle 100 weight 11
The amount is 0.01 to 10 parts by weight. The dispersion medium may be any solvent that does not dissolve the polymer particles.For example, one of water, ethylene glycol, glycerin, methanol, and ethanol, or a mixture of two or more thereof, is exemplified, but it is usually used. Water is preferred.
この方法では、容器の一端を開放して重合体粒子と分散
媒とを同時に1!器内よりも低圧の雰囲気下に放出する
が、このときの容器内の圧力は揮発性発泡剤の蒸気圧以
上または以下のいずれでもよく・放出する雰囲気は通常
常圧の雰囲気が選ばれる。In this method, one end of the container is opened and the polymer particles and the dispersion medium are mixed at the same time. It is discharged into an atmosphere with a lower pressure than the inside of the container, but the pressure inside the container at this time may be either higher than or lower than the vapor pressure of the volatile blowing agent.The atmosphere to be discharged is normally selected to be a normal pressure atmosphere.
このようKして得られる予備発泡粒子は1発泡時の温度
、圧力等によっても異なるが通常3〜60倍の見掛は発
泡倍率を有する。The pre-expanded particles obtained in this manner usually have an apparent expansion ratio of 3 to 60 times, although this varies depending on the temperature, pressure, etc. at the time of one expansion.
この予備発泡粒子内次いで例えば常温、常圧下3〜72
時間程度熟成され2次いて無機ガスまたは無機ガスと揮
発性発泡剤との混合ガスによJ) 0.3〜8kg/f
f1(G)で3〜72時間加圧熟成され、この加圧熟成
によって予備発泡粒子内KO33〜51’#/aII(
G)好ましくは3kf/j(G)以下の内圧が付与され
る。Inside this pre-expanded particle, for example, 3 to 72
0.3 to 8 kg/f
f1 (G) for 3 to 72 hours, and this pressure aging causes KO33 to 51'#/aII (
G) An internal pressure of preferably 3 kf/j (G) or less is applied.
ここで無機ガスとしてれ、空気、窒素、アルゴン。Here, the inorganic gases are air, nitrogen, and argon.
ヘリウム等が用いられる。Helium or the like is used.
なお、予備発泡粒子が加圧熟成*KL、かるべき内圧を
有する場合は、加圧熟成社会らずしも必要ではない。Note that, if the pre-expanded particles have pressure ripening*KL and a suitable internal pressure, pressure ripening is not necessary.
本発明では、予備発泡粒子の内圧と見掛は発泡倍率が式
:0.01軍≦P乙0.5 m (式中、P拡予備発泡
粒子の内圧(ゆ/m(G)) 2mは予備発泡粒子の見
掛は発泡倍率をそれぞれ示す。〕で表わされる関係を有
するポリプロピレン系樹脂予備発泡粒子が用いられる。In the present invention, the internal pressure of the pre-expanded particles and the apparent expansion ratio are calculated using the formula: 0.01≦P0.5 m (wherein, the internal pressure of the P-expanded pre-expanded particles (Y/m (G)) 2 m is The appearance of the pre-expanded particles indicates the expansion ratio.] Pre-expanded polypropylene resin particles are used which have the following relationship.
内圧が0.01m未満の場合および0.5 mを超える
場合には、成型時1通常の水蒸気量でれ融着状態が悪(
(0,Siaを超える場合には成型体内部の融着が悪い
)、良好な成型体は得られず、融着状態を改善するため
に水蒸気量を多くすると成型体の収縮が大きくなってし
まい実用的でなく、また水蒸気を多量用いるため冷却水
を多量必要とし、結局多量のエネルギーを消費するため
コスト高となり、かつ生産性も低下する。予備発泡粒子
の内圧と見掛は発泡倍率f14IK好ましい範囲は式:
0.015m≦P≦0.1 m (式中、Pおよび翼は
前記と同じ意味を有する。)で表わされる範囲である。If the internal pressure is less than 0.01 m or more than 0.5 m, the fusion state may be poor due to the normal amount of water vapor during molding (1).
(If it exceeds 0, Sia, the fusion inside the molded body is poor), a good molded body cannot be obtained, and if the amount of water vapor is increased to improve the fusion state, the shrinkage of the molded body increases. It is not practical, and since it uses a large amount of water vapor, it requires a large amount of cooling water, which ultimately consumes a large amount of energy, resulting in high costs and reduced productivity. The internal pressure and appearance of pre-expanded particles are the expansion ratio f14IK, and the preferred range is the formula:
The range is 0.015 m≦P≦0.1 m (in the formula, P and blades have the same meanings as above).
本発!jlにおいて、予備発泡粒子の見掛は発泡倍率と
は、予備発泡粒子の見掛は密度を重合体粒子の樹脂密度
で除し良値の逆数である。ここで予備発泡粒子の見掛社
密度社例えば所定容積のメスシリンダーに予備発泡粒子
を充填した後重量を一定し1重量/体積により求められ
る。The real deal! In jl, the apparent expansion ratio of the pre-expanded particles is the reciprocal of the apparent density of the pre-expanded particles divided by the resin density of the polymer particles. Here, the density of the pre-expanded particles is determined by filling a graduated cylinder with a pre-expanded volume with the pre-expanded particles and keeping the weight constant, for example, 1 weight/volume.
本発明において、予備発泡粒子の内圧を例えば加圧熟成
によシ付与した場合において1粒子内に導入されるガス
を例えば空気とし友場合、予備発泡粒子の内圧は9次式
:
(式中、0.082社気体定数、tは気温。In the present invention, when the internal pressure of the pre-expanded particles is imparted by, for example, pressure aging, and the gas introduced into each particle is, for example, air, the internal pressure of the pre-expanded particles is determined by the following formula: 0.082 gas constant, t is temperature.
1.0332は*tm−をゆ/−に変換するための係数
を示す。)
Kよ)求めることができる。1.0332 indicates a coefficient for converting *tm- to yu/-. ) K) can be found.
上記の如き予備発泡粒子を用いて成型するKJiってれ
、予備発泡粒子を閉鎖し得るが密閉し得ない金型に充填
し1例えば1.0〜L 5 kII/cj(G) o水
蒸気を用いて加熱膨張させ、m;11シorttm体を
得ることができる。When molding is performed using the pre-expanded particles as described above, the pre-expanded particles are filled into a mold that can be closed but cannot be sealed, and then filled with water vapor of 1.0 to 1.0 to L5 kII/cj (G) o. A m;11 orttm body can be obtained by heating and expanding the m;
本発明により得られるボップロピレン系樹脂発泡成型体
は、緩衡材、包装材、車輌部材、II築資材1食品*a
、断熱材、浮揚材等に用いることができる。The BOPP propylene resin foam molded product obtained by the present invention can be used as a buffering material, a packaging material, a vehicle component, II construction material 1 food*a
It can be used for insulation materials, flotation materials, etc.
以上説明したように9本発明は、見掛は発泡倍率と内圧
0@係を特定し九予備発泡粒子を用いて*mすることに
よシ9粒子関の融着状態が良好で成型時の収縮が少ない
優れた性質の発泡成型体を得ることができる。As explained above, the present invention specifies the apparent expansion ratio and internal pressure of 0@, and uses pre-expanded particles to achieve a good fusion state of the particles during molding. It is possible to obtain a foamed molded product with excellent properties and less shrinkage.
以下、実施例および比較例を掲げて本発明をさらに詳細
にvl明する。Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.
実11〜6および比較例1〜5
エチレン−プロピレンランダム共重合体樹脂粒子(実1
1〜6)100重量部、第1表に示す量のジクロルシフ
0ロメタン、酸化アルミニウム0.5重量部および水2
50重量部を密閉容器内に入れ、攪拌下、第1表に示す
所定温度に昇温し。Examples 11 to 6 and Comparative Examples 1 to 5 Ethylene-propylene random copolymer resin particles (Example 1
1-6) 100 parts by weight, dichloromethane in the amounts shown in Table 1, 0.5 parts by weight of aluminum oxide and 2 parts by weight of water.
50 parts by weight was placed in a closed container, and the temperature was raised to the predetermined temperature shown in Table 1 while stirring.
容器内の圧力を約30 ky/j(G)K保持しながら
容器の一端を開放し、樹脂粒子と水とを同時に大気下へ
放出し、乾燥して第1表に示す見掛は発泡倍率を有する
種々の予備発泡粒子を得た。While maintaining the pressure inside the container at about 30 ky/j (G)K, open one end of the container, release the resin particles and water into the atmosphere at the same time, and dry them to give the apparent foaming ratio shown in Table 1. Various pre-expanded particles were obtained.
得られた予備発泡粒子を常温常圧にて5o時間放置した
後、25℃、 0.3〜6. Ok&/j (G)の空
気にて50時間加圧熟成して第1表に示す内圧を付与し
た。しかる後成瀧用金型に充填し、13〜6.5ゆ/j
(G)の水蒸気圧にて酸層を行なりえ。得られた威薯体
の融着状mシよび収縮の度合いを調べた。The obtained pre-expanded particles were left at room temperature and pressure for 5 hours, and then heated at 25°C for 0.3-6. Pressure aging was carried out for 50 hours in Ok&/j (G) air to give the internal pressure shown in Table 1. After that, fill the mold for forming waterfall and 13 to 6.5 yu/j.
Perform the acid layer at the water vapor pressure of (G). The degree of fusion and shrinkage of the resulting specimen was examined.
Claims (1)
≦P≦0.5 wL(式中、P社予備発泡粒子の内圧(
k#/aj(G)) 、 11社予備発泡粒子の見掛は
発泡倍率をそれぞれ示す。)で表わされる関係を有する
ポリプロピレン系樹脂予備発泡粒子を用いて酸部するこ
とを臀黴とするポリプロピレン系樹脂発泡成層体の製造
方法。The internal pressure and apparent expansion ratio of pre-expanded particles are expressed by the formula: 0.01m
≦P≦0.5 wL (in the formula, the internal pressure of Company P pre-expanded particles (
k#/aj(G)), the appearance of pre-expanded particles from 11 companies indicates the expansion ratio, respectively. ) A method for producing a foamed polypropylene resin laminate, which involves treating pre-expanded polypropylene resin particles with an acid moiety.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56149806A JPS5943493B2 (en) | 1981-09-22 | 1981-09-22 | Manufacturing method of polypropylene resin foam molding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56149806A JPS5943493B2 (en) | 1981-09-22 | 1981-09-22 | Manufacturing method of polypropylene resin foam molding |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5852328A true JPS5852328A (en) | 1983-03-28 |
JPS5943493B2 JPS5943493B2 (en) | 1984-10-22 |
Family
ID=15483114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56149806A Expired JPS5943493B2 (en) | 1981-09-22 | 1981-09-22 | Manufacturing method of polypropylene resin foam molding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5943493B2 (en) |
-
1981
- 1981-09-22 JP JP56149806A patent/JPS5943493B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5943493B2 (en) | 1984-10-22 |
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