JPS6249303B2 - - Google Patents
Info
- Publication number
- JPS6249303B2 JPS6249303B2 JP55027006A JP2700680A JPS6249303B2 JP S6249303 B2 JPS6249303 B2 JP S6249303B2 JP 55027006 A JP55027006 A JP 55027006A JP 2700680 A JP2700680 A JP 2700680A JP S6249303 B2 JPS6249303 B2 JP S6249303B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- ethylene
- heat
- ccl
- foaming
- 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
- 229920000642 polymer Polymers 0.000 claims description 17
- 238000005187 foaming Methods 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 7
- 239000004033 plastic Substances 0.000 claims description 7
- 239000004604 Blowing Agent Substances 0.000 claims description 6
- 229920001971 elastomer Polymers 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000005060 rubber Substances 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 claims description 4
- 239000002667 nucleating agent Substances 0.000 claims description 4
- 229920005676 ethylene-propylene block copolymer Polymers 0.000 claims description 3
- 238000000034 method Methods 0.000 description 23
- 239000006260 foam Substances 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000004088 foaming agent Substances 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229920005629 polypropylene homopolymer Polymers 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229920001821 foam rubber Polymers 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L59/00—Thermal insulation in general
- F16L59/14—Arrangements for the insulation of pipes or pipe systems
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Molding Of Porous Articles (AREA)
- Thermal Insulation (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
本発明は優れた耐熱性及び断熱性を有する断熱
管の製造方法の改良に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a method for manufacturing a heat insulating tube having excellent heat resistance and heat insulation properties.
従来断熱管は金属管の外側に発泡倍率2〜3倍
程度のポリエチレン発泡体による断熱層を形成せ
しめて製品としているものである。然しながら近
時省エネルギー化が必要不可欠とされ、放熱ロス
の少い断熱層として高発泡倍率を有する架橋ポリ
エチレン又はゴム発泡体を金属管の外側に被覆し
ているものであるが、これらの発泡体を被覆する
場合、その製造工程が極めて複雑であると共にコ
スト高となるという欠点があつた。 Conventionally, a heat insulating pipe is a product in which a heat insulating layer made of polyethylene foam having an expansion ratio of about 2 to 3 times is formed on the outside of a metal pipe. However, in recent years, energy saving has become essential, and the outside of the metal tube is coated with cross-linked polyethylene or rubber foam with a high expansion ratio as a heat insulating layer with low heat dissipation loss. In the case of coating, the manufacturing process is extremely complicated and costs are high.
又従来ポリプロピレン発泡体の製造法としてポ
リプロピレンを揮発性溶剤を用いて直接押出す方
法もあるがこの方法をポリプロピレン発泡断熱層
を有する断熱管の製造に応用した場合は次の欠点
を有するものである。この方法では高発泡ポリプ
ロピレン発泡体を製造することが出来るが、ポリ
プロピレンホモポリマーでは融点以下数10度(例
えば130℃程度)の如く、低温度にしなければな
らず、しかも2〜3℃いう厳しい温度制御を必要
とする。その結果、上記断熱管の製造に用いる場
合金属管の外側に、ポリマーを押出す際、金属管
からの冷却に影響されやすく良好な発泡押出が出
来ないものである。 Furthermore, as a conventional method for producing polypropylene foam, there is a method of directly extruding polypropylene using a volatile solvent, but when this method is applied to the production of heat-insulating pipes having a polypropylene foam heat-insulating layer, it has the following drawbacks. . With this method, highly expanded polypropylene foam can be produced, but with polypropylene homopolymer, the temperature must be kept as low as several tens of degrees below the melting point (for example, about 130 degrees Celsius), and moreover, the temperature must be kept at a severe temperature of 2 to 3 degrees Celsius. Requires control. As a result, when the polymer is extruded to the outside of the metal tube when used for manufacturing the above-mentioned heat-insulating tube, it is easily affected by cooling from the metal tube, and good foam extrusion cannot be achieved.
また従来法では上記の如くポリプロピレンホモ
ポリマーを使用しているため発泡剤にはCCl2F−
CClF2などのような常温常圧で液体の特定の発泡
剤しか使用することが出来ず、そのため発泡後発
泡組織が収縮してしまい、断熱管の製造にはかか
る従来法は使用、不可能のものである。 In addition, since the conventional method uses polypropylene homopolymer as mentioned above, CCl 2 F− is used as a blowing agent.
Only certain foaming agents that are liquid at room temperature and pressure, such as CClF 2 , can be used, and as a result, the foam structure shrinks after foaming, making it impossible to use conventional methods for manufacturing insulated pipes. It is something.
更にこの方法による場合には曲げ加工を行うと
その表面にわれ、又はひびを発生するおそれがあ
つた。 Furthermore, when this method is used, there is a risk that the surface will crack or crack when the bending process is performed.
本発明はかかる欠点を改善せんとして鋭意研究
を行つた結果、耐熱性並に断熱性に優れ、しかも
工程が容易にして且つ低コストの断熱管の製造方
法を見出したものである。即ち本発明方法はエチ
レン1〜15%を含有するエチレン−プロピレンブ
ロツク共重合体60〜90重量%とプラスチツク又は
ゴム40〜10重量%とからなる混合ポリマー100重
量部に気泡核形成剤0.1〜10重量部及び発泡剤と
してCCl3F、CClF2−CClF2、CCl2F2から選ばれ
た1種又は2種以上を主体とする揮発性溶剤を
夫々添加した組成物を金属管の外側に押出し加熱
発泡せしめることを特徴とするものである。 The present invention has been made as a result of intensive research aimed at improving these drawbacks, and as a result has discovered a method for manufacturing an insulated tube that has excellent heat resistance and heat insulation properties, is easy to process, and is low cost. That is, in the method of the present invention, 100 parts by weight of a mixed polymer consisting of 60 to 90% by weight of an ethylene-propylene block copolymer containing 1 to 15% of ethylene and 40 to 10% by weight of plastic or rubber are added with 0.1 to 10 parts by weight of a cell nucleating agent. A composition to which a volatile solvent mainly consisting of one or more selected from CCl 3 F, CClF 2 -CClF 2 and CCl 2 F 2 is added as a foaming agent is extruded to the outside of a metal tube. It is characterized by heating and foaming.
本発明方法によれば、上記の如く混合ポリマー
を使用することにより押出操作が容易にして且つ
長時間安定して操業が行いうるものであるが、そ
の理由は次の如くと推考される。即ち通常プラス
チツクを発泡せしめるにおいて最適なポリマーの
弾性は、ずり弾性率が2×106〜5×106dyn/cm2
とされている。ポリマーを揮発性溶剤により発泡
せしめる発泡機構は押出機内のポリマーを溶剤で
膨潤せしめ融点以下の温度で押出機ダイスより押
出せしめ、しかも更に溶剤の蒸発潜熱を利用して
冷却させつつ一気に発泡させるものであるが、こ
の間に上記の如き数値の発泡に適した弾性率をも
つ状態になるものと考えられる。 According to the method of the present invention, by using the mixed polymer as described above, the extrusion operation can be facilitated and the operation can be carried out stably for a long time.The reasons for this are thought to be as follows. That is, the optimal polymer elasticity for foaming plastics is usually a shear modulus of 2×10 6 to 5×10 6 dyn/cm 2 .
It is said that The foaming mechanism that foams a polymer with a volatile solvent swells the polymer in an extruder with a solvent, extrudes it from an extruder die at a temperature below its melting point, and further uses the latent heat of vaporization of the solvent to cool it and foam it all at once. However, it is thought that during this time it will be in a state where it has an elastic modulus suitable for foaming with the above numerical value.
なお溶剤を使用する場合には従来はポリマーを
140℃以下の温度にしなければならないと共にそ
の適正温度範囲は±2℃の如く極めて狭いもので
あるが、本発明方法においてはポリマーは融点以
下10℃程度の範囲においても十分高発泡のものを
うることが出来、その適正温度範囲も±6℃の如
く広いものである。 When using solvents, conventionally polymers were used.
The temperature must be 140°C or lower, and the appropriate temperature range is extremely narrow, such as ±2°C, but in the method of the present invention, the polymer can be foamed to a sufficiently high degree even within a range of about 10°C below its melting point. The appropriate temperature range is as wide as ±6°C.
又本発明方法において発泡剤として常温常圧の
下で揮発性気体を使用しうる理由については次の
如くと推考される。即ち従来方法においてはポリ
マーは著しく低温にしなければならないため、常
温常圧にて液体の蒸発潜熱の大きい溶剤を使用し
なければならないが、本発明方法においてはポリ
マーはその融点以下の近傍にて高発泡化せしめう
るため常温、常圧にてガス状の溶剤を使用するこ
とが出来る。 The reason why a volatile gas can be used as a blowing agent at room temperature and pressure in the method of the present invention is considered to be as follows. In other words, in the conventional method, the polymer must be kept at an extremely low temperature, and a solvent with a high latent heat of vaporization must be used as a liquid at room temperature and pressure, but in the method of the present invention, the polymer has a high temperature near its melting point. A gaseous solvent can be used at room temperature and pressure because it can cause foaming.
又本発明方法においては発泡後の断熱層に収縮
が全くおこらず表面平滑美麗なものをうることが
出来る。 In addition, in the method of the present invention, the heat insulating layer after foaming does not undergo any shrinkage and can have a smooth and beautiful surface.
なお本発明方法により得た断熱管は曲げ加工を
行つたとしても、何等われを生じないものであ
る。 Note that the heat insulating tube obtained by the method of the present invention does not exhibit any cracks even if it is bent.
次に本発明方法において、混合ポリマーとして
MI0.1〜40、エチレン1〜15%を含有するエチレ
ン−プロピレン共重合体を使用する理由は、押出
時における溶融弾性率が前記の如く2×106〜5
×106dyn/cm2であり且つ耐熱性に優れているた
めである。従つて押出条件に厳しい制限を必要と
せず容易にポリマーを押出すことが出来るもので
ある。又この共重合体に混合可能なプラスチツ
ク、ゴムを配合する理由は該共重合体に適度の軟
性を附与せしめるためである。即ち本発明方法に
おいては低温にて押出発泡を行うため、発泡体が
脆くなるおそれがあるが、上記の如くプラスチツ
ク、ゴムを添加することにより、この脆性を改善
するものである。 Next, in the method of the present invention, as a mixed polymer
The reason for using an ethylene-propylene copolymer containing MI 0.1-40 and ethylene 1-15% is that the melt modulus during extrusion is 2 x 10 6 - 5 as mentioned above.
This is because it is 10 6 dyn/cm 2 and has excellent heat resistance. Therefore, the polymer can be easily extruded without requiring severe restrictions on extrusion conditions. The reason why plastics and rubbers that can be mixed with this copolymer are blended is to impart appropriate flexibility to the copolymer. That is, in the method of the present invention, since extrusion foaming is carried out at a low temperature, there is a risk that the foam will become brittle, but this brittleness can be improved by adding plastic or rubber as described above.
このゴムとしては、エチレン−プロピレンゴ
ム、ポリイソブチレン、シス1・4ポリブタジエ
ン、ブチルゴム等はプラスチツクとしてはポリブ
テン−1、低、中、高密度ポリエチレン、エチレ
ン−酢酸ビニルコポリマー、エチレン−αオレフ
イン(プロピレン)コポリマー等である。特にプ
ロピレン成分が10〜60重量%望ましくは20〜50重
量%含有のエチレン−プロピレンゴムが好まし
い。 Examples of this rubber include ethylene-propylene rubber, polyisobutylene, cis 1.4 polybutadiene, butyl rubber and plastics such as polybutene-1, low, medium and high density polyethylene, ethylene-vinyl acetate copolymer, ethylene-α olefin (propylene). copolymers, etc. In particular, ethylene-propylene rubber containing a propylene component of 10 to 60% by weight, preferably 20 to 50% by weight is preferred.
なおプラスチツクゴムの添加量を10〜40重量%
に限定した理由は10重量%未満では、発泡体の脆
性を改善することが出来ず、40重量%を越えると
好適な粘弾性のものがえられず気泡が破れ高倍率
の発泡体をうることが出来ない。 The amount of plastic rubber added should be 10 to 40% by weight.
The reason for this limitation is that if it is less than 10% by weight, the brittleness of the foam cannot be improved, and if it exceeds 40% by weight, suitable viscoelasticity cannot be obtained and the bubbles will burst, resulting in a foam with a high magnification. I can't.
又本発明方法において使用する核形成剤として
は微粉末シリカ、炭酸カルシウム、クレー、ホウ
酸、酒石酸等であるが、特に微粉末のシリカが好
ましい。 Nucleating agents used in the method of the present invention include finely powdered silica, calcium carbonate, clay, boric acid, tartaric acid, etc., and finely powdered silica is particularly preferred.
なおその添加量を0.1〜10重量部特に0.5〜40重
量部と限定したが、その理由は、0.1重量部未満
の場合には微細気泡の発泡体をうることが出来
ず、又10重量部を越えた場合には発泡体が脆くな
るためである。 The amount added was limited to 0.1 to 10 parts by weight, especially 0.5 to 40 parts by weight, because if it was less than 0.1 part by weight, it would not be possible to obtain a foam with fine cells; This is because if it exceeds the limit, the foam becomes brittle.
又本発明方法において使用する発泡剤として、
CCl3F、CClF2−CClF2、CCl2F2に限定した理由
は、この発泡剤により得た発泡体を断熱管の断熱
層として使用した場合、該断熱層にしわ、収縮等
がおこらないためである。 Further, as a blowing agent used in the method of the present invention,
The reason for limiting CCl 3 F, CClF 2 -CClF 2 and CCl 2 F 2 is that when the foam obtained with this foaming agent is used as a heat insulating layer of a heat insulating pipe, wrinkles, shrinkage, etc. will not occur in the heat insulating layer. It's for a reason.
この発泡剤をポリマー内に圧入する方法として
はベントタイプスクリユーを使用してシリンダ中
途よりベント部に圧入すればよい。 The blowing agent can be press-fitted into the polymer by using a vent-type screw and press-fitting it into the vent part from the middle of the cylinder.
又これらに顔料、各種充填材、難熱材、酸化防
止剤、銅害防止剤、紫外線防止剤等を添加しても
よい。 Further, pigments, various fillers, heat retardants, antioxidants, copper damage inhibitors, ultraviolet inhibitors, etc. may be added to these.
而して本発明方法は上記の如き混合ポリマーに
核形成剤及び発泡剤を添加した組成物を通常の工
程により金属管の外側に押出し、加熱発泡せしめ
ればよい。 According to the method of the present invention, a composition prepared by adding a nucleating agent and a foaming agent to the above-mentioned mixed polymer is extruded to the outside of a metal tube through a conventional process, and the mixture is heated and foamed.
次に本発明方法の実施例について説明する。 Next, examples of the method of the present invention will be described.
実施例 1
エチレン−プロピレンブロツク共重合体(エチ
レン成分4%、MI0.7)80重量%とエチレンプロ
ピレンゴム(プロピレン成分26重量%)20重量%
からなる混合ポリマー100重量部に微粉末シリカ
10重量部ベントタツプ65mmφの押出機に供給して
溶融混練した後、該押出機のベルト部にCCl2F26
重量部を圧入し、該ポリマー中に溶解させ、クロ
スヘツド内を通過する15.88φの銅パイプの外側
に上記組成物を158℃にて押出発泡せしめて断熱
層を形成せしめて断熱銅管をえた。Example 1 80% by weight of ethylene-propylene block copolymer (ethylene component: 4%, MI 0.7) and 20% by weight of ethylene propylene rubber (propylene component: 26% by weight)
A mixed polymer consisting of 100 parts by weight of finely powdered silica
After supplying 10 parts by weight to an extruder with a vent tap of 65 mmφ and melting and kneading, CCl 2 F 2 6 was added to the belt section of the extruder.
A weight part was press-fitted and dissolved in the polymer, and the above composition was extruded and foamed at 158°C on the outside of a 15.88φ copper pipe passing through the crosshead to form a heat insulating layer to obtain a heat insulating copper pipe.
斯くして得た断熱銅管における断熱層の気泡径
は細く、その密度は0.08g/m2であつた。 In the thus obtained heat-insulating copper tube, the bubble diameter of the heat-insulating layer was small, and its density was 0.08 g/m 2 .
実施例 2
揮発性発泡剤としてCCl2F2とCCl3Fとを1:
1にて混合したものを10重量部を使用した以外は
すべて実施例1と全く同様にして、断熱銅管をえ
た。Example 2 CCl 2 F 2 and CCl 3 F as volatile blowing agents at 1:1
A heat-insulating copper tube was obtained in the same manner as in Example 1 except that 10 parts by weight of the mixture in Example 1 was used.
この断熱銅管の断熱層は細目にして、密度は
0.042g/m2であつた。 The insulation layer of this insulated copper pipe is fine and the density is
It was 0.042g/ m2 .
以上詳述した如く本発明方法によれば耐熱性及
び断熱性に優れ、給湯用、暖房用として極めて有
用なものである。 As detailed above, the method of the present invention has excellent heat resistance and heat insulation properties, and is extremely useful for hot water supply and space heating.
Claims (1)
ピレンブロツク共重合体60〜90重量%とプラスチ
ツク、又はゴム40〜10重量%とからなる混合ポリ
マー、100重量部に気泡核形成剤0.1〜10重量部及
び発泡剤としてCCl3F、CClF2−CClF2、CCl2F2
から選ばれた1種又は2種以上を主体とする揮発
性溶剤を夫々添加した組成物を金属管の外側に押
出し発泡せしめることを特徴とする断熱管の製造
方法。1 100 parts by weight of a mixed polymer consisting of 60 to 90% by weight of an ethylene-propylene block copolymer containing 1 to 15% of ethylene and 40 to 10% by weight of plastic or rubber, and 0.1 to 10 parts by weight of a cell nucleating agent. and CCl 3 F, CClF 2 −CClF 2 , CCl 2 F 2 as blowing agents.
1. A method for producing a heat insulating tube, which comprises extruding and foaming a composition containing one or more volatile solvents selected from the following to the outside of a metal tube.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2700680A JPS56122841A (en) | 1980-03-04 | 1980-03-04 | Production of heat insulating pipe |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2700680A JPS56122841A (en) | 1980-03-04 | 1980-03-04 | Production of heat insulating pipe |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56122841A JPS56122841A (en) | 1981-09-26 |
JPS6249303B2 true JPS6249303B2 (en) | 1987-10-19 |
Family
ID=12209025
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2700680A Granted JPS56122841A (en) | 1980-03-04 | 1980-03-04 | Production of heat insulating pipe |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56122841A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008275146A (en) * | 2007-04-06 | 2008-11-13 | Sekisui Chem Co Ltd | Composite pipe and its manufacturing method |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58208327A (en) * | 1982-05-30 | 1983-12-05 | Dainichi Nippon Cables Ltd | Resin composition for molding heat-insulating foam layer |
JPS60255834A (en) * | 1984-05-31 | 1985-12-17 | Idemitsu Petrochem Co Ltd | Production of polypropylene resin foam |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2411949C2 (en) * | 1974-03-13 | 1984-09-06 | Kabel- und Metallwerke Gutehoffnungshütte AG, 3000 Hannover | Process for the continuous production of heat-insulated line pipes |
JPS543874A (en) * | 1977-06-13 | 1979-01-12 | Mitsui Toatsu Chem Inc | Molded product of foamed polypropylene and vessel therefrom |
-
1980
- 1980-03-04 JP JP2700680A patent/JPS56122841A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008275146A (en) * | 2007-04-06 | 2008-11-13 | Sekisui Chem Co Ltd | Composite pipe and its manufacturing method |
Also Published As
Publication number | Publication date |
---|---|
JPS56122841A (en) | 1981-09-26 |
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