JPS60130630A - Production of polyurethane foam - Google Patents

Production of polyurethane foam

Info

Publication number
JPS60130630A
JPS60130630A JP23843083A JP23843083A JPS60130630A JP S60130630 A JPS60130630 A JP S60130630A JP 23843083 A JP23843083 A JP 23843083A JP 23843083 A JP23843083 A JP 23843083A JP S60130630 A JPS60130630 A JP S60130630A
Authority
JP
Japan
Prior art keywords
foam
polyol
catalyst
air permeability
thermoplastic resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP23843083A
Other languages
Japanese (ja)
Inventor
Shigeo Kuga
茂夫 久我
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.)
Tachi S Co Ltd
Toyo Quality One Corp
Original Assignee
Tachikawa Spring Co Ltd
Toyo Rubber Chemical Industrial 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 Tachikawa Spring Co Ltd, Toyo Rubber Chemical Industrial Co Ltd filed Critical Tachikawa Spring Co Ltd
Priority to JP23843083A priority Critical patent/JPS60130630A/en
Publication of JPS60130630A publication Critical patent/JPS60130630A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a polyurethane foam excellent in high-frequency sealability, by mixing a specified polyol with a blowing agent, a catalyst, and an organic isocyanate, expansion-molding the mixture and adjusting the air permeability of the obtained foam to a specified value. CONSTITUTION:A polyol containing a thermoplastic resin molecule incorporated in its molecule is mixed with a blowing agent, a catalyst, and an organic isocyanate, and the mixture is expansion-molded so that the air permeability of the foam may be adjusted to 150cc/cm<2>/sec or below. Said polyol can be produced by incorporating a molecule of a thermoplastic resin such as vinyl chloride in producing a polyol by copolymerizing a stating material such as ethylene glycol with ethylene oxide or the like. The adjustment of air permeability is performed by adjusting the amount of a catalyst. Generally, the air permeability is decreased by decreasing the amount of catalyst.

Description

【発明の詳細な説明】 本発明は、高周波融着性に優れたポリウレタンフォーム
の製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a polyurethane foam with excellent high frequency weldability.

この種のウレタンフオームは、表地及び裏地を被覆し、
高周波加工して、車輛用内装材、あるいはクッション上
張シ材などに使用されている。この高周波融着性を有す
るポリウレタンフォームを製造する方法として、熱可塑
性樹脂を添加混合する方法及び熱可塑性樹脂液を含浸さ
せる方法が知られている。
This type of urethane foam covers the outer material and lining,
It is subjected to high-frequency processing and used for vehicle interior materials and cushion upholstery materials. As methods for manufacturing polyurethane foam having high-frequency fusion properties, there are known methods of adding and mixing a thermoplastic resin and methods of impregnating the foam with a thermoplastic resin liquid.

前者の方法は、所定のs91Jウレタン原料にナイロン
樹脂、ポリ塩化ビニル樹脂、アクリル樹脂等の高周波融
着性に優れた熱可塑性樹脂粉末を同時に添加混合して、
ポリウレタンフォームを得る方法である。
The former method involves simultaneously adding and mixing thermoplastic resin powder with excellent high frequency fusion properties such as nylon resin, polyvinyl chloride resin, and acrylic resin to a predetermined S91J urethane raw material.
This is a method of obtaining polyurethane foam.

この方法では、熱可塑性樹脂を多く添加すれば、それだ
け高周波融着性が向上するが、その反面ポリウレタンフ
ォームが持つ本来の物理的特性(引張強さ、引裂強さ、
伸縮特性など)が低下してしまう問題がある。
In this method, the more thermoplastic resin is added, the higher the high-frequency fusion properties are.
There is a problem that the elastic properties (such as elastic properties) deteriorate.

また後者の方法は、ポリウレタンフォームを任意の厚さ
く通常3 mm〜20朋位)にスライスした後、ポリ塩
化ビニルペースト、アクリルエマルジョンなどの熱可塑
性樹脂液を含浸させ、これを乾燥又はキュアーさせて高
周波融着性を持たせる方法である。
The latter method involves slicing polyurethane foam into pieces of arbitrary thickness (usually about 3 mm to 20 mm), impregnating them with a thermoplastic resin liquid such as polyvinyl chloride paste or acrylic emulsion, and drying or curing them. This is a method of imparting high frequency fusion properties.

しかしこの方法の場合も、ポリウレタンフォームの持つ
本来の物理的特性が低下するとともに、反1発弾性が低
下し、触感も著しく悪くなる欠点がある。
However, this method also has the disadvantage that the original physical properties of the polyurethane foam are degraded, the one-shot resilience is degraded, and the tactile sensation is also significantly poor.

本発明は、これらの問題を解消すべくなされたもので、
ポリウレタンフォームの物理的特性を損うことなく、高
周波融着性を高めることができるポリウレタンフォーム
の製造方法を得んとするものである。
The present invention was made to solve these problems.
The object of the present invention is to provide a method for producing polyurethane foam that can improve high-frequency fusion properties without impairing the physical properties of the polyurethane foam.

すなわち本発明は、熱可塑性樹脂の分子をポリオールの
分子中に組み入れたJ IJオールと発泡剤と触媒と有
機インシアネートとを混合して発泡成形し、フオームの
通気性を150 CL/cnr” /1dec以下に調
整することを特徴とする。また上記混合物に更にリン酸
エステル系難燃剤を加えて発泡成形することを特徴とす
る。
That is, in the present invention, JIJol, in which thermoplastic resin molecules are incorporated into polyol molecules, is mixed with a blowing agent, a catalyst, and an organic incyanate, and foam molded, and the air permeability of the foam is increased to 150 CL/cnr''/ It is characterized in that the temperature is adjusted to 1 dec or less. It is also characterized in that a phosphate ester flame retardant is further added to the above mixture and foam molding is carried out.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

ポリオールの分子中に熱可塑性樹脂の分子を組み入れた
ポリオールを用意する。この、l IJオ−ルハ、エチ
レングリコール、ジエチレングリコール、ゾロピレング
リコール、ブチレングリコール(2官能)、グリ士リン
、トリメチロール7’ Gl ノ9ン、トリメチロール
エタン(3官能)、ペンタエリスリトール、エチレンジ
アミン、α−メチルグリコツト(4官能)等の出発物質
に酸化プロピレン、酸化エチレン、酸化ブチレン、酸化
スチレンなどを重合してポリオールを作る際ニ塩化ビニ
ール、アクリル等の熱可塑性樹脂の分子を組み入れるこ
とにより製造される。この場合、熱可塑性樹脂の比率は
、ウレタン7オームの物理的特性と、高周波融着性とを
勘案して20〜60重量係が重量しい。
A polyol having thermoplastic resin molecules incorporated into the polyol molecule is prepared. This lIJ-olha, ethylene glycol, diethylene glycol, zolopylene glycol, butylene glycol (bifunctional), glycerin, trimethylol 7' Gl 9-9, trimethylolethane (trifunctional), pentaerythritol, ethylenediamine, When producing polyols by polymerizing propylene oxide, ethylene oxide, butylene oxide, styrene oxide, etc. to a starting material such as α-methyl glycostate (tetrafunctional), molecules of thermoplastic resins such as vinyl dichloride and acrylic are incorporated. Manufactured. In this case, the ratio of the thermoplastic resin is preferably 20 to 60% by weight, taking into account the physical properties of 7 ohm urethane and high frequency fusion properties.

次いでこのポリオールに発泡剤と触媒と有機インシアネ
ートと必要に応じて添加剤を混合する。発泡剤として、
水、トリクロロモノフロロメタン、メチレンクロライド
等が挙げられる。
Next, this polyol is mixed with a blowing agent, a catalyst, an organic incyanate, and, if necessary, additives. As a foaming agent,
Examples include water, trichloromonofluoromethane, methylene chloride, and the like.

触媒にはアミン触媒、錫触媒などがあり、アミン触媒と
してエチレンジアミン、トリメチルアミン、nエチルモ
ルホリン、トリエタノールアミン等が挙げられ、錫触媒
としてスターナスオクトエート、ジグチルチンジラウレ
ート等が挙げられる。有機インシアネートには、トリレ
ンジインシアネート、ジフェニルメタンジイソシアネー
ト、ナフタレンジイソシアネート等が挙げられる。また
必要に応じて添加する添加剤として着色剤、難燃剤、充
填剤などが挙げられる。
Catalysts include amine catalysts and tin catalysts; amine catalysts include ethylenediamine, trimethylamine, n-ethylmorpholine, triethanolamine, and the like; tin catalysts include starus octoate, digtyltine dilaurate, and the like. Examples of organic incyanates include tolylene diisocyanate, diphenylmethane diisocyanate, naphthalene diisocyanate, and the like. Additionally, colorants, flame retardants, fillers, etc. may be mentioned as additives that may be added as necessary.

これらの添加量は特に限定されるものではないが、通常
ポリオール100重量部に対し発泡剤(水の場合)2.
0〜7.0重量部、触媒0.03〜1.0重級部、が好
ましい。
The amount of these added is not particularly limited, but usually 2.
0 to 7.0 parts by weight and 0.03 to 1.0 parts by weight of catalyst are preferred.

これら混合物の発泡成形は、常法に従ってワンショット
法あるいはブレ号?リマー法などによシおこなうが、得
られるウレタンフオームの通気性が150鎮/α”7s
ec以下、好ましくは5〜150 cc/cm2/ s
eeになるように調整する。この調整方法は、触媒の量
を調整することによシおこなう。即ち、一般的に触媒の
量を少くすることによυ、通気性を低く抑えることがで
きる。
Foam molding of these mixtures is carried out using the one-shot method or the blurring method according to conventional methods. Although this is done by the reaming method, the air permeability of the resulting urethane foam is 150mm/α"7s.
ec or less, preferably 5 to 150 cc/cm2/s
Adjust so that it becomes ee. This adjustment method is carried out by adjusting the amount of catalyst. That is, generally by reducing the amount of catalyst, the air permeability can be kept low.

ここで通気性を150 CC/crn2/ see以下
としたのは、上限を越えると高周波加工の際、高周波の
通電時間を多く必要とし、ス・ぐ−りが発生しやすく、
劣化、焼は焦げが生じ外観が非常に悪くなるためである
The reason why the air permeability is set to 150 CC/crn2/see or less is that if the upper limit is exceeded, high frequency energization time will be required during high frequency processing, and soot and goo will easily occur.
This is because deterioration and burning cause scorching and the appearance becomes very poor.

このようにして得られたポリウレタンフォームは、高周
波融着性の良い熱可塑性樹脂の分子をJ IJオールの
分子中に組み入れているので、ポリウレタンフォームの
物理的特性を保持した状態で高周波融着性を向上するこ
とができる。
The polyurethane foam obtained in this way has thermoplastic resin molecules with good high frequency fusion properties incorporated into the molecules of J IJ All, so it has high frequency fusion properties while retaining the physical properties of polyurethane foam. can be improved.

しかもポリウレタンフォームの各個所T (D 高周波
融着性を均一とすることができる。
Furthermore, the high frequency fusion properties can be made uniform at each location T (D) of the polyurethane foam.

更にウレタンフオームの通気性が150cc/Cm27
 SeC以下なので、高周波の通電時間が短く、極板の
電流が少ないため、ス・臂−りの発生がない。従ってこ
のことによって、尚周波融着性を高めることができる。
Furthermore, the breathability of the urethane foam is 150cc/cm27
Since it is less than SeC, the high frequency current application time is short and the current in the electrode plate is small, so there is no occurrence of sagging or bending. Accordingly, this makes it possible to improve the frequency weldability.

又本ポリウレタンフォームは高周波融着の他に熱融着、
超音波llI!I!層等他の融着手段を用いても良いこ
とは勿論である。
In addition to high frequency welding, this polyurethane foam can also be heat fused,
Ultrasonic II! I! Of course, other fusing means such as layers may also be used.

次に第2の発明につき説明する。Next, the second invention will be explained.

この発明は、上述した第1の発明においてポリオールに
発泡剤と触媒と有機インシアネートと難燃剤とを混合す
る際、難燃剤としてリン酸エステル系難燃剤を使用する
方法である。この難燃剤としてはリン酸トリクレジル、
リン酸トリフェニル、リン酸トリー2−エチルヘキシル
などがある。この難燃剤の添加量は、難燃効果を考慮し
てポリオール100重量部に対して15〜30M量部が
好適である。
This invention is a method of using a phosphate ester flame retardant as a flame retardant when mixing a blowing agent, a catalyst, an organic incyanate, and a flame retardant with a polyol in the first invention described above. The flame retardant is tricresyl phosphate,
Examples include triphenyl phosphate and tri-2-ethylhexyl phosphate. The amount of this flame retardant added is preferably 15 to 30 M parts per 100 parts by weight of the polyol in consideration of the flame retardant effect.

このようにリン酸エステル系難燃剤を加えたポリウレタ
ンフォームは、他の難燃剤を使用した場合に比べて高周
波加工時のス・ぞ−りの発生がなく、よシ高周波融着性
を高めることができる。このことは、本発明者が実験に
より明らかとしたものである。
In this way, polyurethane foams containing phosphate ester flame retardants do not cause scratches during high-frequency processing compared to cases where other flame retardants are used, and have improved high-frequency fusion properties. I can do it. This fact was clarified by the inventor through experiments.

次に本発明の実施例につき説明する。Next, examples of the present invention will be described.

実施例工 下記組成の配合物をワンショット法にて発泡成形し、フ
オーム密度0.023.通気度53 cc/(’m2/
 8611! の軟質ポリウレタンフォームラ得り。
Example Work A compound having the following composition was foam-molded using a one-shot method, and the foam density was 0.023. Air permeability 53 cc/('m2/
8611! Made of soft polyurethane foam.

このようにして得られたウレタンフオームを厚さ10I
lII+にスライスして1.ff IJエステル系線繊
維表地とナイロン糸不織布の黒地とを)*層し高周波加
工機により電流3.3A、通′酊時間17秒にて高周波
加工を行った。この積層体の剥離強度を調べた結果、3
.0 kl?/30 *tIと潰れたものであった。
The urethane foam thus obtained has a thickness of 10I.
Slice into lII+ 1. ff IJ ester line fiber outer material and black nylon thread nonwoven fabric were layered) and subjected to high frequency processing using a high frequency processing machine at a current of 3.3 A and a drying time of 17 seconds. As a result of examining the peel strength of this laminate, 3
.. 0 kl? /30 *tI and crushed.

またウレタンフオームは、引張強さ1.10に9/er
r?、又このポリウレタンフォームの物理的特性を調べ
たところ、引張強さ1.10 kg/m” 、引裂強さ
Q、 6 kg/lyn 、伸び160チで、ポリウレ
タンフォームの持つ特性が良好に維持されていた。
In addition, the urethane foam has a tensile strength of 1.10 and 9/er.
r? Furthermore, when the physical properties of this polyurethane foam were investigated, the properties of the polyurethane foam were well maintained, with a tensile strength of 1.10 kg/m'', a tear strength of 6 kg/lyn, and an elongation of 160 inches. was.

以上の結果から明らかなように本発明によれば、ポリオ
ールの分子中に熱可塑性樹脂を組込むことと、フオーム
の通気性を150 cc/crn2/sec以下とする
ことにより、ウレタンフォームトシての物理的特性を低
下することなく高周波融着性を著しく高め、更に難燃剤
としてリン酸エステル系のものを使用することによシ、
高周波融着性をより高めることができる顕著な効果を奏
する0
As is clear from the above results, according to the present invention, the physical properties of urethane foam can be improved by incorporating a thermoplastic resin into the polyol molecule and by controlling the air permeability of the foam to 150 cc/crn2/sec or less. By significantly increasing high-frequency fusion properties without deteriorating physical properties, and by using a phosphate ester-based flame retardant,
0 which has a remarkable effect of further increasing high frequency fusion properties.

Claims (2)

【特許請求の範囲】[Claims] (1) 熱可塑性樹脂の分子をポリオールの分子中に組
み入れたポリオールと発泡剤と触媒と有機インシアネー
トとを混合して発泡成形し、フオームの通気性を150
 cc/cm2/ sec以下に調整することを特徴と
するポリウレタンフォームの製造方法。
(1) A polyol in which thermoplastic resin molecules are incorporated into polyol molecules, a blowing agent, a catalyst, and an organic incyanate are mixed and foam-molded to increase the air permeability of the foam to 150%.
A method for producing polyurethane foam, which comprises adjusting the foam to cc/cm2/sec or less.
(2)熱可塑性樹脂の分子をポリオールの分子中に組み
入れたポリオールと発泡剤と触媒と有機イソシアネート
とリン酸エステル系難燃剤とを混合して発泡成形し、フ
オームの通気性を150 CC/1yn2/ see以
下に調整することを特徴とするポリウレタンフォームの
製造方法。
(2) A polyol in which a thermoplastic resin molecule is incorporated into a polyol molecule, a blowing agent, a catalyst, an organic isocyanate, and a phosphoric acid ester flame retardant are mixed and foam-molded, and the air permeability of the foam is 150 CC/1yn2. A method for producing polyurethane foam, characterized by adjusting the foam to less than /see.
JP23843083A 1983-12-17 1983-12-17 Production of polyurethane foam Pending JPS60130630A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23843083A JPS60130630A (en) 1983-12-17 1983-12-17 Production of polyurethane foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23843083A JPS60130630A (en) 1983-12-17 1983-12-17 Production of polyurethane foam

Publications (1)

Publication Number Publication Date
JPS60130630A true JPS60130630A (en) 1985-07-12

Family

ID=17030087

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23843083A Pending JPS60130630A (en) 1983-12-17 1983-12-17 Production of polyurethane foam

Country Status (1)

Country Link
JP (1) JPS60130630A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2236106A (en) * 1989-09-21 1991-03-27 British Vita Weldable polyurethane foam
GB2256871A (en) * 1991-06-20 1992-12-23 British Vita Weldable polyurethane foam

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2236106A (en) * 1989-09-21 1991-03-27 British Vita Weldable polyurethane foam
GB2256871A (en) * 1991-06-20 1992-12-23 British Vita Weldable polyurethane foam

Similar Documents

Publication Publication Date Title
US4438221A (en) Polyurethane foam-filled foams and method of producing same
US4683246A (en) Polyurethane foam-fiber composites
DE102013221693B4 (en) Sound absorbing material for a vehicle, method of manufacturing the same and laminate comprising the sound absorbing material
US4439548A (en) Modified polyurethane product having improved load-bearing characteristics
US10654984B2 (en) Heterogeneous foam composition and method
CA1318996C (en) Vandal resistant seat
CN101665579A (en) Method for manufacturing opening foaming material and compositions thereof
CN107614615A (en) Introduce the thermoplastic polyurethane for being available for Jiao Lian Wei Ge and the method for crosslinked foaming is carried out using it
JPS60130630A (en) Production of polyurethane foam
US3772219A (en) Flexible polyurethane foam composition
US3535196A (en) Method for the formation of composite structures based on expanded polyurethane material welded to a covering layer
US3840628A (en) Manufacture of resilient compound foams
US4482582A (en) Modified polyurethane product having improved load bearing characteristics
JP4745671B2 (en) Method for producing polyurethane foam having open cell structure
JP2006131755A (en) Soft polyurethane foam
JPH03109444A (en) Production of crosslinked polyolefin resin foam
JPH018355Y2 (en)
JPH0121795Y2 (en)
Szycher Flexible and semiflexible foams
JPH0912667A (en) Molded flexible polyurethane foam
JPS61152720A (en) Production of soft polyurethane foam laminatable by flame lamination
JPH0216338B2 (en)
US4348489A (en) Dielectrically modified polyurethane foam material
JP3606655B2 (en) Molded ceiling material for automobile and manufacturing method thereof
JP3356824B2 (en) Thermoplastic resin composition