JPH01149840A - Production of foamed resin article - Google Patents
Production of foamed resin articleInfo
- Publication number
- JPH01149840A JPH01149840A JP62308248A JP30824887A JPH01149840A JP H01149840 A JPH01149840 A JP H01149840A JP 62308248 A JP62308248 A JP 62308248A JP 30824887 A JP30824887 A JP 30824887A JP H01149840 A JPH01149840 A JP H01149840A
- Authority
- JP
- Japan
- Prior art keywords
- foaming
- resin
- titanium
- foaming agent
- average particle
- 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.)
- Pending
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 21
- 239000011347 resin Substances 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 238000005187 foaming Methods 0.000 claims abstract description 16
- 239000002245 particle Substances 0.000 claims abstract description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 6
- 239000010936 titanium Substances 0.000 claims abstract description 6
- 239000006260 foam Substances 0.000 claims description 12
- 239000004604 Blowing Agent Substances 0.000 claims description 5
- 238000007664 blowing Methods 0.000 claims description 3
- 239000012943 hotmelt Substances 0.000 claims description 3
- 239000004088 foaming agent Substances 0.000 abstract description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract description 4
- 238000000576 coating method Methods 0.000 abstract description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 abstract description 3
- 239000011882 ultra-fine particle Substances 0.000 abstract description 3
- 239000004156 Azodicarbonamide Substances 0.000 abstract description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 abstract description 2
- 235000019399 azodicarbonamide Nutrition 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract description 2
- 239000011261 inert gas Substances 0.000 abstract description 2
- 229920001684 low density polyethylene Polymers 0.000 abstract description 2
- 239000004702 low-density polyethylene Substances 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract 3
- 229910001873 dinitrogen Inorganic materials 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- -1 polypropylene Polymers 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229920001780 ECTFE Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000019406 chloropentafluoroethane Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- NKZSPGSOXYXWQA-UHFFFAOYSA-N dioxido(oxo)titanium;lead(2+) Chemical compound [Pb+2].[O-][Ti]([O-])=O NKZSPGSOXYXWQA-UHFFFAOYSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000002666 chemical blowing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 1
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 239000000178 monomer 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
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000001294 propane Substances 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
- 239000004711 α-olefin Substances 0.000 description 1
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)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、電線の被覆をはじめ、シート、ホース、チュ
ーブ等への適用に好適な樹脂発泡体の製造方法に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for producing a resin foam suitable for application to electric wire coatings, sheets, hoses, tubes, and the like.
[従来の技術]
樹脂は、発泡させることにより電気特性、可撓性、熱絶
縁性等の各種特性の向上を図れるばかりでなく、軽量化
、低価格化も図れるため、幅広い用途に適用されている
。[Prior art] Resin is used in a wide range of applications because foaming not only improves various properties such as electrical properties, flexibility, and thermal insulation, but also makes it lighter and cheaper. There is.
従来、樹脂発泡体は、熱溶融押出可能な樹脂、発泡剤及
び発泡助剤を押出機に導入し、これらを均一に分散させ
てから押出して発泡させることにより製造されておりζ
発泡助剤としては窒化硼素が一般に使用されている。Conventionally, resin foams have been manufactured by introducing a hot-melt extrudable resin, a blowing agent, and a blowing aid into an extruder, uniformly dispersing these, and then extruding and foaming.
Boron nitride is commonly used as a foaming aid.
[発明が解決しようとする問題点]
近年、樹脂発泡体の発泡度を70%以上に高発泡化する
ことが各方面で検討されているが、上記した従来の製造
方法では、高発泡化することが極めて困難であり、特に
厚さ1mm以下の発泡体の場合に難しい。[Problems to be Solved by the Invention] In recent years, increasing the degree of foaming of resin foams to 70% or more has been studied in various fields. This is extremely difficult, especially for foams with a thickness of 1 mm or less.
本発明は、上記に基づいてなされたものであり、70%
以上の高発泡体を容易に得ることができる樹脂発泡体の
製造方法の提供を目的とするものである。The present invention has been made based on the above, and 70%
The object of the present invention is to provide a method for producing a resin foam that can easily produce the above-described highly foamed product.
[問題点を解決するための手段]
本発明の樹脂発泡体の製造方法は、発泡助剤として平均
粒径が0.2μm以下のチタン系超微粒子を用いること
を特徴とするものである。[Means for Solving the Problems] The method for producing a resin foam according to the present invention is characterized by using ultrafine titanium particles having an average particle size of 0.2 μm or less as a foaming aid.
本発明において、熱溶融押出し可能な樹脂としては、低
密度ポリエチレン、中密度ポリエチレン、高密度ポリエ
チレン、ポリプロピレン、エチレン−αオレフィン共重
合体、エチレン−酢酸ビニル共重合体、エチレンとアク
リル系モノマとの共重合体、ポリブタンなどがあげられ
る。また、テトラフルオロエチレン−パーフルオロアル
キルビニルエーテル共重合体(PFA)、テトラフルオ
ロエチレン−ヘキサフルオロプロピレン共重合体(FE
P)、エチレン−テトラフルオロエチレン共重合体(E
TFE)、エチレン−クロロトリフルオロエチレン共重
合体(ECTFE)、ビニリデンフルオライド(PVd
F)などのふっ素糸樹脂もあげられる。In the present invention, hot melt extrudable resins include low density polyethylene, medium density polyethylene, high density polyethylene, polypropylene, ethylene-α olefin copolymer, ethylene-vinyl acetate copolymer, and combinations of ethylene and acrylic monomers. Examples include copolymers and polybutane. In addition, tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), tetrafluoroethylene-hexafluoropropylene copolymer (FE)
P), ethylene-tetrafluoroethylene copolymer (E
TFE), ethylene-chlorotrifluoroethylene copolymer (ECTFE), vinylidene fluoride (PVd
Fluorine thread resins such as F) can also be mentioned.
発泡剤としては、アゾジカルボンアミド、4,4′−オ
キシビスベンゼンスルホニルヒドラジド等の化学発泡剤
、窒素、アルゴン、炭酸ガス等の不活性気体、メタン、
プロパン、ブタン、ペンタン等の炭化水素、ジクロロジ
フルオロメタン、ジクロロモノフルオロメタン、モノク
ロロジフルオロメタン、モノクロロペンタフルオロエタ
ン、トリクロロモノフルオロメタン、トリクロロトリフ
ルオロメタン等のハリゲン化ぶつ化炭化水素といったも
のがあげられる。Examples of blowing agents include chemical blowing agents such as azodicarbonamide and 4,4'-oxybisbenzenesulfonyl hydrazide, inert gases such as nitrogen, argon, and carbon dioxide, methane,
Examples include hydrocarbons such as propane, butane, and pentane, and halogenated fluorinated hydrocarbons such as dichlorodifluoromethane, dichloromonofluoromethane, monochlorodifluoromethane, monochloropentafluoroethane, trichloromonofluoromethane, and trichlorotrifluoromethane.
発泡剤の添加方法としては、予め樹脂に発泡剤を含浸、
溶解させてもよく、また、押出機中に発泡剤を注入する
方法でもよい。The method of adding the foaming agent is to impregnate the resin with the foaming agent in advance,
It may be dissolved or a blowing agent may be injected into an extruder.
発泡助剤として使用されるチタン系超微粒子は、チタン
を含むものであればよく、酸化チタン、−酸化チタン、
チタン酸ジルコン酸鉛、チタン酸鉛、ランタン酸・ジル
コン酸・チタン酸鉛を代表とする。結晶形状は、アナタ
ーゼ型、ルチル型、アモルファスのいずれでもよいが、
平均粒径が0.2μm以下のものを使用することにより
、発泡度を著しく向上することが可能となる。特に、0
.05μm以下が好ましい。The titanium-based ultrafine particles used as a foaming aid may be those containing titanium, such as titanium oxide, -titanium oxide,
Representative examples include lead zirconate titanate, lead titanate, and lanthanic acid/zirconate/lead titanate. The crystal shape may be anatase type, rutile type, or amorphous, but
By using particles with an average particle size of 0.2 μm or less, the degree of foaming can be significantly improved. In particular, 0
.. The thickness is preferably 0.05 μm or less.
なお、樹脂発泡体は架橋、非架橋のいずれでもよい。架
橋する場合は、電子線、γ線等の電離性放射線の照射に
よる方法が好ましい。Note that the resin foam may be either crosslinked or non-crosslinked. In the case of crosslinking, a method using irradiation with ionizing radiation such as electron beams and gamma rays is preferred.
[発明の実施例]
第1表の各側に示す成分からなるコンパウンドを押出機
のホッパーから供給し、押出機の中間部でモノクロロペ
ンタフルオロエタンを4〜6kg/Cm”Gの圧力で注
入して溶融樹脂中に均一に分散させてから外径0.3m
mの導体外周に押出し被覆して厚さ0.3mmの発泡絶
縁被覆を形成した。[Embodiments of the Invention] A compound consisting of the components shown on each side of Table 1 was fed from the hopper of an extruder, and monochloropentafluoroethane was injected at a pressure of 4 to 6 kg/Cm''G in the middle of the extruder. After uniformly dispersing it in the molten resin, the outer diameter is 0.3 m.
A foamed insulating coating with a thickness of 0.3 mm was formed by extrusion coating on the outer periphery of the conductor.
なお、発泡体の押出条件は、30 m m押出機を用い
、L/D = 25、圧縮比−2,5である。シリンダ
の設定温度は、ポリエチレンの場合は180℃、ふっ素
樹脂の場合は290℃である。The extrusion conditions for the foam were as follows: using a 30 mm extruder, L/D = 25, and compression ratio -2.5. The set temperature of the cylinder is 180°C for polyethylene and 290°C for fluororesin.
実施例及び比較例の発泡絶縁被覆の発泡度について評価
した結果を第1表に示す。なお、発泡度は次式から求め
た。Table 1 shows the results of evaluating the degree of foaming of the foamed insulation coatings of Examples and Comparative Examples. Note that the degree of foaming was determined from the following formula.
発泡度−(1−(ρ/ρ。)] X100 [%1(
ρ:発泡体の比重、ρ。:非発泡体の比重)第1表から
明らかな通り、実施例1〜5では70%以上の高発泡体
が得られたのに対し、比較例1〜3では60%程度の発
泡度しか達成できなかった。Foaming degree-(1-(ρ/ρ.)] X100 [%1(
ρ: Specific gravity of the foam, ρ. : Specific gravity of non-foamed material) As is clear from Table 1, in Examples 1 to 5, highly foamed products of 70% or more were obtained, whereas in Comparative Examples 1 to 3, only about 60% of foaming was achieved. could not.
「発明の効果」
以上説明してきた通り、本発明によれば70%を越える
高発泡の樹脂発泡体を容易に実現することができる。"Effects of the Invention" As explained above, according to the present invention, a resin foam with a high foaming rate exceeding 70% can be easily realized.
7一71
Claims (1)
出機に導入し、溶融樹脂中に発泡剤及び発泡助剤を均一
に分散させてから押出して樹脂発泡体を製造する方法に
おいて、上記発泡助剤として平均粒径が0.2μm以下
のチタン系超微粒子を用いることを特徴とする樹脂発泡
体の製造方法。(1) In a method of manufacturing a resin foam by introducing hot-melt extrudable resin, a blowing agent, and a blowing aid into an extruder, uniformly dispersing the blowing agent and blowing aid in the molten resin, and then extruding the resin. . A method for producing a resin foam, characterized in that ultrafine titanium particles having an average particle size of 0.2 μm or less are used as the foaming aid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62308248A JPH01149840A (en) | 1987-12-04 | 1987-12-04 | Production of foamed resin article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62308248A JPH01149840A (en) | 1987-12-04 | 1987-12-04 | Production of foamed resin article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01149840A true JPH01149840A (en) | 1989-06-12 |
Family
ID=17978722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62308248A Pending JPH01149840A (en) | 1987-12-04 | 1987-12-04 | Production of foamed resin article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01149840A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5622663A (en) * | 1995-06-14 | 1997-04-22 | Dow Corning Corporation | Method for preparing a continuous foam profile containing a filamentary core |
WO2003000792A1 (en) * | 2001-06-26 | 2003-01-03 | Daikin Industries, Ltd. | Resin composition, process for production thereof, and foam-insulated electric wire |
JP2011073209A (en) * | 2009-09-29 | 2011-04-14 | Dainippon Printing Co Ltd | Foamed decorative sheet |
-
1987
- 1987-12-04 JP JP62308248A patent/JPH01149840A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5622663A (en) * | 1995-06-14 | 1997-04-22 | Dow Corning Corporation | Method for preparing a continuous foam profile containing a filamentary core |
WO2003000792A1 (en) * | 2001-06-26 | 2003-01-03 | Daikin Industries, Ltd. | Resin composition, process for production thereof, and foam-insulated electric wire |
US7241826B2 (en) | 2001-06-26 | 2007-07-10 | Daikin Industries, Ltd. | Resin composition, process for production thereof, and foam-insulated electric wire |
JP2008174752A (en) * | 2001-06-26 | 2008-07-31 | Daikin Ind Ltd | Resin composition and method for producing it and foam-insulated electric wire |
US7884148B2 (en) * | 2001-06-26 | 2011-02-08 | Daikin Industries, Ltd. | Resin composition, method of producing same, and foam-insulated electric wire |
JP2012001733A (en) * | 2001-06-26 | 2012-01-05 | Daikin Industries Ltd | Resin composition, method of producing same, and foam-insulated electric wire |
JP2011073209A (en) * | 2009-09-29 | 2011-04-14 | Dainippon Printing Co Ltd | Foamed decorative sheet |
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