JPS5862025A - Manufacture of polycarbonate foamed body - Google Patents

Manufacture of polycarbonate foamed body

Info

Publication number
JPS5862025A
JPS5862025A JP56161137A JP16113781A JPS5862025A JP S5862025 A JPS5862025 A JP S5862025A JP 56161137 A JP56161137 A JP 56161137A JP 16113781 A JP16113781 A JP 16113781A JP S5862025 A JPS5862025 A JP S5862025A
Authority
JP
Japan
Prior art keywords
polycarbonate
mold
molded body
temperature
melting point
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
Application number
JP56161137A
Other languages
Japanese (ja)
Other versions
JPS634502B2 (en
Inventor
Kiyoyasu Fujii
藤井 清康
Koichi Horikawa
堀川 宏一
Yoichi Mikami
三上 陽一
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP56161137A priority Critical patent/JPS5862025A/en
Publication of JPS5862025A publication Critical patent/JPS5862025A/en
Publication of JPS634502B2 publication Critical patent/JPS634502B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING 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
    • B29K2069/00Use of PC, i.e. polycarbonates or derivatives thereof, as moulding material

Abstract

PURPOSE:To obtain a foamed body that has been uniformly and highly foamed, by heating a polycarbonate molded body impregnated with an organic solvent to at least its melting point in a mold, then cooling it to a specified temperature, and releasing the pressure in an approximately closed mold to allow it to foam. CONSTITUTION:The molded body of polycarbonate[e.g. polycarbonate prepared from carbonic acid and 2,2-bis(4-oxyphenyl) propane]is impregnated with an organic solvent having a boiling point lower than the glass transition point of said polycarbonate (e.g. cychlohexane and trichlorotrifluoroethane), then the molded body is introduced in a mold, is heated under pressure to a temperature of at least the melting point of said polycarbonate, and then is cooled to a temperature range of from the glass transition temperature to the melting point. Then the pressure is released, and the molded body is allowed to foam in an approximately closed mold to obtain a highly foamed polycarbonate molded body. If the foaming is effected in an approximately closed mold diverged in one direction, a foamed body having elongated cells and a skin can be obtained. USE:Dielectric material, heat insulating materials, and construction materials.

Description

【発明の詳細な説明】 本発明はポリカーボネート成形体から発泡体を製造する
方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing foam from polycarbonate moldings.

ポリカーボネート発泡体はそのすぐれた性質。Polycarbonate foam has excellent properties.

たとえば良好な電気的性質、高い耐熱性、良好な絨械的
性質、高い耐老化性、良好な耐水性等により、櫨々の用
途、たとえば断熱材料、鑓築材料等に好適に用いられる
ものである。
For example, due to its good electrical properties, high heat resistance, good carpeting properties, high aging resistance, and good water resistance, it is suitable for use in concrete applications such as insulation materials and construction materials. be.

従来よりポリカーボネートの発泡体は、他の熱町閣性樹
脂の発泡体と同様に熱分解型発泡剤又は揮発性有5ta
1剤を発泡剤として使用して製造する方法が知られてい
る。
Conventionally, polycarbonate foams, like other thermoplastic resin foams, have been made using thermally decomposable blowing agents or volatile foams.
A manufacturing method using one agent as a blowing agent is known.

しかしながら熱分解型発泡剤は分解するとアミノ基、=
ト”9ル基等O窒素を含む基を有する化金物が残存する
たハポリカーボ本−トが分解されるという欠点を有して
お参、揮発性有JIIail剤は上記欠点はないが、有
aim剤が含浸されたものを加熱し有機溶剤を気化膨張
することにより発泡させるため低倍率の発泡体しか得ら
れないという欠点を有していた。
However, when the thermally decomposable blowing agent decomposes, the amino group, =
However, volatile JIIail agents do not have the above disadvantages, but they do have the disadvantage that the hapolycarbohydrate remains decomposed due to metal compounds containing O nitrogen-containing groups such as nitrogen groups. Since foaming is performed by heating the material impregnated with the agent and vaporizing and expanding the organic solvent, it has the disadvantage that only a foam with a low magnification can be obtained.

本発明の目的は上記欠点に鑑み発泡剤として有機溶剤を
使用し、高倍率の発泡体を製造する方法を提供すること
にある。又本発明の他の目的は表皮層を有し1強度の大
きい発泡体を製造する方法を提供するととkある。
SUMMARY OF THE INVENTION In view of the above drawbacks, it is an object of the present invention to provide a method for producing a foam with a high magnification by using an organic solvent as a blowing agent. Another object of the present invention is to provide a method for producing a foam having a skin layer and high strength.

即ち本発明O罫Wは。That is, the O-ruled W of the present invention is.

1 ポリカーボネート成形体に、該ボリカーボネー)0
ガラス転移温度より低い沸点を有する有機溶剤を含浸せ
しめ、成形用型に供給し、該型内で加圧しながら該ポリ
カーボネートの融点以上に加熱した後、該ポリカーボネ
ートのガラス転移温度〜融点の鉱度@固に冷却し。
1 Polycarbonate molded body, the polycarbonate) 0
The polycarbonate is impregnated with an organic solvent having a boiling point lower than the glass transition temperature, supplied to a mold, and heated in the mold to a temperature higher than the melting point of the polycarbonate while being pressurized. Cool thoroughly.

次いで解圧して略密閉された型内で発泡させることを特
徴とするポリカーボネート発泡体O製造方法及び 2、ポリカーボネート成形体に、該ポリカーボネートの
ガラス転移温度より低い沸点を有する有S嬉剤を含浸せ
しめ、成形用111c供給し。
A method for producing a polycarbonate foam O, which is characterized in that the pressure is then decompressed and the foam is foamed in a substantially sealed mold; , supplying 111c for molding.

該型内で加圧しながら該ポリカーボネートの融点以上に
加熱した黴、該ポリカーボネートOガフχ転移温度〜融
点の温度軸@に急冷し。
The mold is heated to a temperature above the melting point of the polycarbonate while being pressurized in the mold, and then rapidly cooled to a temperature axis from the polycarbonate O guff χ transition temperature to the melting point.

とを特徴とするポリカーボネートOIl造方法に存する
A method for producing polycarbonate oil is provided.

本発明vcおいて使用するポリカーボネートとは、炭酸
とグリコール又はビスフェノールとのポリエステルであ
って、分子flAKジフェニルアルカンを有する芳香族
ポリカーボネートは、結晶性がよく、融点が高く、耐熱
性、耐候性、耐酸性がすぐれているので好ましい、上記
芳香族ポリカーボネートとしては、たとえば2.2−ビ
ス(4−オキシフェニル)プロパン、 X、Z−ビス(
4−オキシフェニル)ブタン、1.1−ビス(4−第4
ジフエニル)シクロヘキサン、1.1−ビス(4−オキ
シフェール)ブタン、1.1−ビス(4−オキシフェニ
ル)インブタン、1.1−ビス(4−オキシフェニル)
エタン等のビスフェノールからのポリカーボネートがあ
げられる・ 本発明においては上記ポリカーボネートは成形体となさ
れるが、成形方法社従来公如O任意の方法が採用されて
よ(、たとえば押出成形。
The polycarbonate used in the VC of the present invention is a polyester of carbonic acid and glycol or bisphenol, and the aromatic polycarbonate having the molecule flAK diphenylalkane has good crystallinity, high melting point, heat resistance, weather resistance, and acid resistance. Examples of the above-mentioned aromatic polycarbonates, which are preferable because of their excellent properties, include 2,2-bis(4-oxyphenyl)propane, X,Z-bis(
4-oxyphenyl)butane, 1,1-bis(4-quaternary)
diphenyl)cyclohexane, 1.1-bis(4-oxyphenyl)butane, 1.1-bis(4-oxyphenyl)inbutane, 1.1-bis(4-oxyphenyl)
Examples include polycarbonates made from bisphenols such as ethane. In the present invention, the polycarbonate is formed into a molded body, but any conventional molding method may be employed (for example, extrusion molding).

射出成形、圧縮成形等があげられる。Examples include injection molding and compression molding.

本発明において使用する有aim剤は上記ポリカーボネ
ートに含浸しうるものであって、ポリカーボネートのガ
ラス転移温度より低い沸点を有するものであり、沸点F
10℃以上であるのが好ましく、たとえばペンタン、イ
ンペンタン、ヘキサン、インへキサン、ヘプタン、オク
タン、シクロヘキサン等の脂肪族炭化水素、トリクロロ
トリフルオロエタン、ジクロロデトフフルオロエタン、
テトラクロgジフルオロエタン峰のフッ素化脂肪族炭化
水素、ベンゼン、トルエン、キシレン等O芳香族炭化水
嵩、ブチルアルコール、プロピルアルコール等のアルコ
ール、エーテルなどがあげられる。そしてポリカーボネ
ートに含浸された際にポリカーボネートと白化したり、
ポリカーボネートと反応しないものが好ましく、ペンタ
ン、インペンタン、ヘプタン、インへブタン、シクロヘ
キサン及びトリクロロトリフルオロエタンが好ましく、
より好ましくはシクロヘキサンとトリクロロトリフルオ
ロエタンである。
The aiming agent used in the present invention is one that can be impregnated into the polycarbonate, has a boiling point lower than the glass transition temperature of the polycarbonate, and has a boiling point of F
The temperature is preferably 10° C. or higher, and examples include aliphatic hydrocarbons such as pentane, impentane, hexane, inhexane, heptane, octane, and cyclohexane, trichlorotrifluoroethane, dichlorodetoffluoroethane,
Examples include fluorinated aliphatic hydrocarbons such as tetrachloride and difluoroethane, aromatic hydrocarbons such as benzene, toluene and xylene, alcohols such as butyl alcohol and propyl alcohol, and ethers. And when it is impregnated with polycarbonate, it turns white with polycarbonate,
Those that do not react with polycarbonate are preferred, and pentane, impentane, heptane, inhebutane, cyclohexane and trichlorotrifluoroethane are preferred;
More preferred are cyclohexane and trichlorotrifluoroethane.

本発明においてrt前記ポリカーボネート成形体に上記
有機溶剤が含浸されるのであるが、含浸方法は公短の任
意の方法が採用されてよく、たとえば圧力容器内にポリ
カーボネート成形体と有機溶剤及び必要−ならばiI[
嵩ガス、炭酸ガス崎の不活性ガス−を供給し、有機溶剤
の沸点以上に加熱し加圧する方法が採用される。
In the present invention, the polycarbonate molded body at rt is impregnated with the organic solvent, and any method, short or short, may be adopted as the impregnation method. For example, the polycarbonate molded body and the organic solvent are placed in a pressure vessel, and if necessary, baii[
A method is adopted in which a bulk gas, an inert gas such as carbon dioxide gas, is supplied, and the organic solvent is heated to a temperature higher than the boiling point and pressurized.

本発明においては有機溶剤が含浸されたポリカーボネー
ト成形体は次に成形用mに供給され、加圧されながらポ
リカーボネートの融点以上に加熱される。上記如μ条件
は特に限定されないがZoo−400秘−〇条件でプレ
スするのが好ましく又加熱条件にポリカーボネートの融
点より10〜40℃高い温度であるのが好ましい。
In the present invention, the polycarbonate molded body impregnated with an organic solvent is then fed to a molding m, and heated to a temperature higher than the melting point of the polycarbonate while being pressurized. The above-mentioned conditions are not particularly limited, but it is preferable to press under Zoo-400 conditions, and the heating condition is preferably 10 to 40° C. higher than the melting point of the polycarbonate.

本発明においては上記加熱加圧後ガラス転移温度〜融点
O11度範圃に冷却するのであるが、冷却は任意の方法
が採用されてよく、たとえば水冷、空冷等O方法あげら
れ、ポリカーボネート成形体は表向温度がガラス転移温
度より10〜40℃高い温度に冷却されるのが好ましい
In the present invention, after heating and pressurizing, the polycarbonate molded body is cooled to a temperature in the range of 11 degrees from the glass transition temperature to the melting point. Any method may be used for cooling, such as water cooling, air cooling, etc. It is preferable that the surface temperature is cooled to a temperature 10 to 40° C. higher than the glass transition temperature.

そして解圧するとポリカーボネート成形体は発泡を始め
るが本発明においてFi発発泡略密閉された型内で行う
、上記発泡は任意の方法が採用されてよく、たとえば解
圧すると共にポリカーボネート成形体を所定0**閉さ
れた金型に供給して発泡させる方法、プレスで加熱加圧
し。
When the pressure is released, the polycarbonate molded body starts foaming, but in the present invention, Fi foaming is carried out in a substantially closed mold. Any method may be used for the above foaming, for example, when the polycarbonate molded body is decompressed, the polycarbonate molded body is *Method of foaming by supplying it to a closed mold, heating and pressurizing it with a press.

冷却した後プレスを拡開し、プレスの周囲にスペイサ−
を設置して発泡させる方法等があげられる。
After cooling, expand the press and place spacers around the press.
Examples include a method of installing foam and foaming.

又ポリカーボネート成形体を成形用型中で融点以上に加
熱加圧した後ガラス転移温度〜融点の温度範vs8c急
冷し、次いで成形用型を一方向に拡−し、拡開されかつ
略密閉された成形用型内で発泡させると、ポリカーボネ
ート成形体はIN−が遣く冷却され内部は冷却されず又
一方向にのみ発泡するので、表皮を有し、一方向に細長
い気泡を有する発泡体が得られる。
In addition, the polycarbonate molded body was heated and pressurized to a temperature above the melting point in a mold, and then rapidly cooled to a temperature range from the glass transition temperature to the melting point vs. When foamed in a mold, the polycarbonate molded body is cooled by IN-, but the inside is not cooled and foams only in one direction, resulting in a foamed body with a skin and elongated cells in one direction. It will be done.

崗ポリカーボネート威形体を製する際にポリカーボネー
トの成形に通常用いられている可履剤や滑剤を添加して
もよいし、又炭酸カルシウム、タルク、クレー、雲母粉
、パーライト、シリカ、カオリン、il祿上等の気泡4
11剤を添加してもよい。
When producing a polycarbonate shaped body, lubricants and lubricants that are commonly used in polycarbonate molding may be added, and calcium carbonate, talc, clay, mica powder, perlite, silica, kaolin, and other additives may be added. fine bubbles 4
11 agents may be added.

本発明の構成は上述のj#)であり、ポリカーボネート
成形体は有機溶剤が含浸され、成形用型内て加熱加圧さ
れた後ガラス転移温度〜融点の温度範囲に冷却されて、
解圧され略密閉型内で発泡されるので、含浸された有J
ll&溶剤は加熱加圧の際に気化して逃散せず、又発泡
の際にも大気中に逃散しないOで均一に発泡された高発
泡倍率の発泡体が得られる。又、急冷し、一方向に拡開
された略密閉型内で発泡されると表皮を有し、一方向に
細長い気泡を有する高発泡倍率の発泡体が得られる。又
本発明で使用する発泡剤は有a#1剤であるから、ポリ
カーボネートが分解するおそれがなく、ポリカーボネー
トの有する電気的性質、機械的性質、耐熱性、耐老化性
、耐水性等の特性が低下することがなく歌熱材料、電気
絶縁材料、am材料等に好適に使用される。
The structure of the present invention is the above-mentioned j#), in which a polycarbonate molded body is impregnated with an organic solvent, heated and pressurized in a mold, and then cooled to a temperature range from the glass transition temperature to the melting point.
Since the pressure is decompressed and foamed in a nearly closed mold, the impregnated
The ll&solvent does not vaporize and escape during heating and pressurization, and does not escape into the atmosphere during foaming, resulting in a foamed product uniformly foamed with O and having a high expansion ratio. Furthermore, when the material is rapidly cooled and foamed in a substantially closed mold expanded in one direction, a foam with a high expansion ratio having a skin and elongated cells in one direction can be obtained. Furthermore, since the blowing agent used in the present invention is an A#1 agent, there is no risk of polycarbonate decomposing, and the properties of polycarbonate such as electrical properties, mechanical properties, heat resistance, aging resistance, and water resistance are maintained. It does not deteriorate and is suitably used for thermal insulation materials, electrical insulation materials, am materials, etc.

次に本発明の製造方法を実施例によ炒説明する。Next, the manufacturing method of the present invention will be explained using examples.

実施例1 プレス板に内形が120X126■の正方形であ抄厚さ
が1MOスペーサーを載置し、スペーサー内に粒状のポ
リカーボネート樹脂〔帝人化虞社製、−品名パンライト
に−1100,2J−ビス(4−オキシフェニル)プロ
パンからのポリカーボネート〕を供給し、280℃、1
50秘−の条件で5分間プレス成形し、ポリカーボネー
ト板を得た。
Example 1 A spacer with a square inner diameter of 120 x 126 cm and a paper thickness of 1 MO was placed on a press plate, and a granular polycarbonate resin [manufactured by Teijin Kago Co., Ltd., product name: Panlite-1100, 2J] was placed inside the spacer. polycarbonate from bis(4-oxyphenyl)propane] and heated at 280°C for 1
Press molding was carried out for 5 minutes at 50°C to obtain a polycarbonate plate.

得られたポリカーボネート板とシクロへ牛サン3tを5
Lの圧力容器に供給し、170℃に保たれたオイルバス
で80分間加熱してポリカーボネート板にシクロヘキサ
ンを含浸せしめた。
Add 3 tons of beef sun to the obtained polycarbonate plate and cyclo
The mixture was supplied to a pressure vessel of 1.5 mm and heated in an oil bath maintained at 170° C. for 80 minutes to impregnate the polycarbonate plate with cyclohexane.

圧力容器内を室温まで冷却した後ポリカーボネート板を
取り出して重蓋を測定したところ、シクロへ牛サンが1
9重量哄含浸していた。
After cooling the inside of the pressure vessel to room temperature, we took out the polycarbonate plate and measured the heavy lid.
It was impregnated with a weight of 9 g.

上記シクロヘキサンが含浸したポリカーボネート板を前
記スペーサーに供給し、前記プレスで240℃、150
4/−の条件で5分間加熱加圧し、加圧したままプレス
の電源を切断して160℃に冷却し、次に解圧すると同
時にプレス板を引き上げスペーサーを内形が3・o x
s s 。
The polycarbonate plate impregnated with cyclohexane was supplied to the spacer, and the plate was heated at 240°C and 150°C in the press.
Heat and pressurize for 5 minutes under the condition of 4/-, turn off the power to the press and cool it to 160℃ while keeping the pressure applied, then simultaneously lift the press plate and place the spacer with an inner diameter of 3.0 x
ss.

■の正方形てあり厚さが9−のスペーサーに取伽代えて
再びプレスし放置したところ、36゜X3fiOX9箇
のポリカーボネート発泡体が得られた1発泡気泡は略球
形であり、均一に分散しており、見掛は比重はQO44
であった。
When I replaced the spacer with a square spacer with a thickness of 9 mm and pressed it again and left it to stand, a 36° x 3fiOX polycarbonate foam with 9 points was obtained.The foamed cells were approximately spherical and were uniformly dispersed. The apparent specific gravity is QO44.
Met.

実施例2 プレス板に内形が1@0X16(1−の正方形で°あり
厚さが1mのスペーサーを載置し、スペーサー内に粒状
のポリカーボネート樹脂〔奇人化成社製、商品名パンラ
イトL−1250,!。
Example 2 A spacer with an inner diameter of 1@0x16 (1-) square with a thickness of 1 m was placed on a press plate, and a granular polycarbonate resin [manufactured by Kijin Kasei Co., Ltd., trade name: Panlite L-] was placed inside the spacer. 1250,!

2−ビス(4−オキシフェニル)プロパンから049カ
ーボネート〕を供給し、ZSO℃、1sOKf/aIi
の条件でS分間プレス成形しポリカーボネート板を得た
049 carbonate] from 2-bis(4-oxyphenyl)propane, ZSO°C, 1sOKf/aIi
A polycarbonate plate was obtained by press molding for S minutes under the following conditions.

得られたポリカーボネート板を使用し実施例1で行った
と同様にシクロヘキサンを含浸せしめたところ1!L8
重量哄含浸した。
When the obtained polycarbonate plate was impregnated with cyclohexane in the same manner as in Example 1, 1! L8
Impregnated by weight.

上記シクロヘキサンが含浸したポリカーボネート板を内
径がxsoxxsoxso(iさ)−である雌金型に供
給し、雄金型で240℃、1504/jO糸件で6分間
加熱加圧し、加圧したまま、水で金型内向が1110℃
になるように急冷し1次に解圧すると共k、雄金型を雄
金型と雌金型との間隔が2s■になるように引き上げて
固定したところ、1l10X180X25のポリカーボ
ネート発泡体が得られた。
The above polycarbonate plate impregnated with cyclohexane was fed into a female mold with an inner diameter of The inward direction of the mold is 1110℃.
When the male mold was pulled up and fixed so that the distance between the male mold and the female mold was 2 seconds, a polycarbonate foam of 1 l 10 x 180 x 25 was obtained. Ta.

得られた発泡体は約1−の表面層を有し、厚さ方向易こ
細長い気泡が均一に分散しており、発泡倍率Fizts
倍であった。
The obtained foam has a surface layer of about 1 -, in which elongated cells that are easy to shrink in the thickness direction are uniformly dispersed, and the foaming ratio is Fizts.
It was double that.

実施例3 プレス板に内形が160X160■の正方形であり、厚
さがas−のスペーサーを1aIIL。
Example 3 A spacer having a square inner shape of 160 x 160 cm and a thickness of as-1 was placed on a press plate.

スペーサー内に粒状Oポリカーボネート樹脂〔奇人化成
社製、商品名パンライ)L−1250W、2!−ビス(
4−オキシフェニル)プロパンからのポリカーボネート
〕を供給し、280℃、180 ?、4−の条件でS分
間プレス成形し、ポリカーボネート板を得た。
Inside the spacer is granular O polycarbonate resin (manufactured by Kijin Kasei Co., Ltd., trade name Panrai) L-1250W, 2! −Bis(
Polycarbonate from 4-oxyphenyl)propane] was supplied at 280°C and 180°C. , 4- for S minutes to obtain a polycarbonate plate.

得られたポリカーボネート板とトリクロロトリフルオロ
エタン3tをStの圧力容器に供給し、170℃に保た
れたオイルパスで3時間加熱してポリカーボネート板に
トリクロロトリフルオロエタンを含浸せしめた。圧力容
器内を室温まで冷却した後ポリカーボネート板を取抄出
して重量を測定したところ、トリクロロトリフルオロエ
タンがla5重量哄含浸していた。
The obtained polycarbonate plate and 3 tons of trichlorotrifluoroethane were supplied to a St pressure vessel and heated in an oil path kept at 170° C. for 3 hours to impregnate the polycarbonate plate with trichlorotrifluoroethane. After cooling the inside of the pressure vessel to room temperature, the polycarbonate plate was taken out and its weight was measured, and it was found that it was impregnated with trichlorotrifluoroethane in an amount of 15 kg by weight.

上記トリクロロトリフルオロエタンが含浸したポリカー
ボネート板を実施例2で使用した雌金IJIK供給し、
雄金型テ240 Kl:、13 OJlz/mO条件で
10分間開熱加圧し、加°圧した家まで水で金型内面が
186’に、なるように急冷し、解圧すると共に雄金型
と雌金型の間隔が20■になるように雄金型を引き上げ
て固定したところ、1@0X160X20■の発泡体が
得られた。
The polycarbonate plate impregnated with the above trichlorotrifluoroethane was supplied to the female gold IJIK used in Example 2,
The male mold was heated and pressurized for 10 minutes under the conditions of 240 Kl:, 13 OJlz/mO, and the pressurized body was rapidly cooled with water until the inner surface of the mold became 186', and as the pressure was released, the male mold and When the male mold was pulled up and fixed so that the distance between the female molds was 20 square, a foam of 1@0×160×20 square was obtained.

得られた発泡体は約(LllllIO表向を有しており
、厚さ方向に細長い気泡が均一に分散しており1発泡倍
率は3&8倍であった。
The obtained foam had a surface of about (LllllIO), elongated cells were uniformly dispersed in the thickness direction, and the foaming ratio was 3 and 8 times.

特許出願人 積水化学工業株式会社 代表者藤沼基利patent applicant Sekisui Chemical Co., Ltd. Representative Mototoshi Fujinuma

Claims (1)

【特許請求の範囲】 L ポリカーボネート成形体に、該ポリカーボネートの
ガラス転移温度より低い沸点を有する有機溶剤を含浸せ
しめ、成形用型に供給し、該型内で加圧しながら該ポリ
カーボネートの融点以上に加熱した後、該ポリカーボネ
ートのガラス転移湿度〜融点の温度範禰に冷却し1次い
で解圧して略W閉された型^で発泡させることを特徴と
するポリカーボネート発泡体の製造方法。 2 ポリカーボネートが芳香族ポリカーボネートである
特許請求の範囲部1項記載の製造方法。 亀 有機溶剤の沸点が0℃以上である特許請求の範11
111項又は第2項ε戟O1l造方法。 表 ポリカーボネート成形体に、該ポリカーボネートの
ガラス転移温度より低い沸点を有する有機溶剤を含浸せ
しめ、成形用型に供給し、該型内で加圧しながら該ポリ
カーボネートの融点以上に加熱した後、該ポリカーボネ
ートのガラス転移感度−一点の温度範囲に急冷し、次い
で成るポリカーボネートの製造方法。 翫 ポリカーボネートか芳香族ポリカーボネートである
特許請求の範囲端4項記載の製造方法。 亀 有機溶剤の沸点が0℃以上である特許請求のm11
14項又Fi第S項記載の製造方法。
[Claims] L A polycarbonate molded body is impregnated with an organic solvent having a boiling point lower than the glass transition temperature of the polycarbonate, supplied to a mold, and heated to a temperature higher than the melting point of the polycarbonate while being pressurized in the mold. After that, the polycarbonate foam is cooled to a temperature range from the glass transition humidity to the melting point of the polycarbonate, and then depressurized and foamed in a substantially W-closed mold. 2. The manufacturing method according to claim 1, wherein the polycarbonate is an aromatic polycarbonate. Tortoise Claim 11 in which the boiling point of the organic solvent is 0°C or higher
Item 111 or Item 2 ε戟O1l manufacturing method. Table: A polycarbonate molded body is impregnated with an organic solvent having a boiling point lower than the glass transition temperature of the polycarbonate, supplied to a mold, and heated to a temperature higher than the melting point of the polycarbonate while pressurizing within the mold. Glass Transition Sensitivity - A method of manufacturing polycarbonate consisting of rapid cooling to a temperature range and then subsequent cooling. The manufacturing method according to claim 4, wherein polycarbonate or aromatic polycarbonate is used. Kame Patent claim m11 in which the organic solvent has a boiling point of 0°C or higher
The manufacturing method described in Section 14 or Fi Section S.
JP56161137A 1981-10-08 1981-10-08 Manufacture of polycarbonate foamed body Granted JPS5862025A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56161137A JPS5862025A (en) 1981-10-08 1981-10-08 Manufacture of polycarbonate foamed body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56161137A JPS5862025A (en) 1981-10-08 1981-10-08 Manufacture of polycarbonate foamed body

Publications (2)

Publication Number Publication Date
JPS5862025A true JPS5862025A (en) 1983-04-13
JPS634502B2 JPS634502B2 (en) 1988-01-29

Family

ID=15729291

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56161137A Granted JPS5862025A (en) 1981-10-08 1981-10-08 Manufacture of polycarbonate foamed body

Country Status (1)

Country Link
JP (1) JPS5862025A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06100724A (en) * 1992-09-18 1994-04-12 Sekisui Plastics Co Ltd Production of synthetic resin expansion molded body good in dimensional stability
JP2007516107A (en) * 2003-05-17 2007-06-21 マイクログリーン・ポリマーズ・インコーポレーテッド Production of fully reusable foamed polymer from recycled materials

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01188806A (en) * 1988-01-22 1989-07-28 Nippon Telegr & Teleph Corp <Ntt> Light receiving device with multi-layer film filter and its manufacture
JPH03223705A (en) * 1989-12-12 1991-10-02 Hitachi Cable Ltd Optical multiplexing/demultiplexing device and optical multiplexing/demultiplexing module

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06100724A (en) * 1992-09-18 1994-04-12 Sekisui Plastics Co Ltd Production of synthetic resin expansion molded body good in dimensional stability
JP2007516107A (en) * 2003-05-17 2007-06-21 マイクログリーン・ポリマーズ・インコーポレーテッド Production of fully reusable foamed polymer from recycled materials

Also Published As

Publication number Publication date
JPS634502B2 (en) 1988-01-29

Similar Documents

Publication Publication Date Title
US5234640A (en) Process of producing thermoplastic polyester series resin foamed
US3812225A (en) Method of manufacturing foamed crosslinked polyolefin slabs involving multiple expansion techniques and direct gas pressure
EP0585378B1 (en) Foam blowing agent composition and process for producing foams
JPH06500806A (en) Sulfone polymer foam produced with aqueous blowing agents
JPWO2016194737A1 (en) Thermoplastic polyurethane expanded particles and molded articles of thermoplastic polyurethane expanded particles
US4925606A (en) Method for enhancing thermal expandability of direct-injection foams
JPH03143933A (en) Expandable granule and method for preparation of foaming material therefrom
EP0186308B1 (en) Expandable polyetherimide compositions and foamed materials obtained therefrom
CA2399239A1 (en) Extruded foam product with reduced surface defects
JPS5862025A (en) Manufacture of polycarbonate foamed body
WO1999040149A1 (en) Polycarbonate resin foam and shock absorber using the same
WO1998025996A1 (en) Expanded particles of polyolefin resin and process for preparing the same
JPH0559140B2 (en)
JPS6097833A (en) Manufacture of expanded crosslinked ethylene polymer molded shape
JPS63500457A (en) Polymer foam, thermoformed product thereof and method for molding the same
EP0785057A2 (en) Process for producing foamed body of polycarbonate resin and foamed body obtained thereby
JPH0680813A (en) Foamed polycarbonate resin having high molecular weight and its production
JPH06100724A (en) Production of synthetic resin expansion molded body good in dimensional stability
JP2902242B2 (en) Foamable resin sheet and method for producing the same
JPS5851123A (en) Method of molding preliminarily foamed polypropylene resin particles in mold
JPH10251437A (en) Molded item of foamed polypropylene resin particle
JPS5867423A (en) Preparation of poly carbonate foam
JPH05255531A (en) Production of molded polymer foam
JP2000109595A (en) Formed article of biodegradable foamed polyester resin particle and foamed particle
JPS61113627A (en) Foamed particle of high-density polyethylene resin and production thereof