JPS5819321A - Production of flame-laminatable, flame-resistant soft polyurethane foam - Google Patents

Production of flame-laminatable, flame-resistant soft polyurethane foam

Info

Publication number
JPS5819321A
JPS5819321A JP56118119A JP11811981A JPS5819321A JP S5819321 A JPS5819321 A JP S5819321A JP 56118119 A JP56118119 A JP 56118119A JP 11811981 A JP11811981 A JP 11811981A JP S5819321 A JPS5819321 A JP S5819321A
Authority
JP
Japan
Prior art keywords
flame
group
foam
flame retardant
polyol
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
JP56118119A
Other languages
Japanese (ja)
Inventor
Yoshio Imai
今井 嘉夫
Tsuneo Asano
浅野 恒夫
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.)
Inoac Corp
Original Assignee
Inoue MTP KK
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 Inoue MTP KK filed Critical Inoue MTP KK
Priority to JP56118119A priority Critical patent/JPS5819321A/en
Publication of JPS5819321A publication Critical patent/JPS5819321A/en
Pending legal-status Critical Current

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Landscapes

  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To produce the titled foam excellent in mechanical properties and wet heat aging resistance, by reacting an organic isocyanate with a specified polyether-polyol in the presence of both of a reactive flame retardant and an additive flame retardant each containing P and/or halogen. CONSTITUTION:The following compoents A, B, C and D are reacted in the presence of small amounts of a blowing agent, a catalyst and a foam stabilizer: (A) an organic isocyanate, (B) a polyether-polyol mixture, MW/OH group 300-2,000, consisting of a trifunctional polyether-polyol and 10-40wt% multifunctional (functionality >=4) polyether-polyol, (C) 1-20wt%, based on total polyol, isocynato group-reactive, P and/or halogen-containing reactive flame retardant (e.g., dibromoneopentyl glycol) reactive with an isocyanate group and (D) additive flame retardant unreactive with isocyanate group contg. 0.5-1.5wt% P based on foam weight, and a halogen in an amount of 20-50 times (calculated as Cl) that of P.

Description

【発明の詳細な説明】 軟質ウレタン7オームは布地など麹の素材と貼−合わせ
て、$’−))ツバ−の如1!自動車内装材として、ま
丸衣料、鞄、ブーツ、カーペットの如き非自動車の会費
に広(使われている。貼勢会破方法としては、接着剤を
使用する方法と、フオームを火炎中高周波ウニβディン
グによって一熔融させて布地などと直maw−sせる方
法とがある。
[Detailed Description of the Invention] The soft urethane 7 ohm can be pasted with a koji material such as cloth, and it will look like $'-)) Tsuba-no-1! It is widely used as an automobile interior material for non-automotive items such as round clothing, bags, boots, and carpets.The pasting method can be broken by using adhesive or by heating the foam with high-frequency sea urchin in a flame. There is a method in which it is melted by β-ding and then maw-sed directly onto fabric.

後者、特に火炎を用−て接着させるフレームフミ冬−ト
法は、乾燥工程が不要であや、接着適度も遣く、設備的
、経済的に有利である。
The latter method, particularly the flame bonding method in which flame is used for adhesion, is advantageous in terms of equipment and economy, as it does not require a drying process and requires a moderate amount of adhesion.

フレームラミネートに使用されるウレタンフオームは、
その用途に応じて種々の物性が要求される。#に衣料中
自動車シートにはいわゆる「へ九秒」の1に%A事、す
なわち圧1IIl!l1iI量の良好な事が必要で60
、まえ高度の難燃性能が要求される。
The urethane foam used for frame laminate is
Various physical properties are required depending on the use. #The so-called "9 seconds" on the car seat in clothing is 1%A, that is, the pressure is 1IIl! It is necessary to have a good amount of l1iI60
, a high degree of flame retardant performance is required.

−毅に離燃性?%//ンフォームと難燃処理され喪布地
をフレーム9ミネートすると、その複合材料は、フオー
ム単体中布地単体に比べて燃やすくなる鎖肉がある。こ
の原因は、両者の燃l11j1度の違−により、Im傭
が持続し九秒、熔融し元ウレタンフオームが布地に浸み
込む、%/%わゆる「田−ソタ現象」によ隻燃焼が促進
されると考えられる。その他フオームとしては、硬度の
大なるものが良く、アレームラ縄ネート調品としては表
面材との接着強度の大暑−事も重要である。しかるに強
度、伸度、硬度、8E****t どの横mmm性質を
十e瀦足に保ち、しかも被接着素材との親合わせK>い
て、十分tkII!着強度を有し、しかも高度の離燃性
能を発揮せしめることは極めて困難であった。
- Is Tsuyoshi flammable? When flame-retardant fabric is laminated with a frame, the composite material becomes more flammable than the fabric alone in the foam. The reason for this is that due to the 1 degree difference in combustion between the two, the temperature lasts for 9 seconds, and the original urethane foam melts and soaks into the fabric, which is the so-called "Tan-Sota phenomenon". It is thought that this will be promoted. Other foams that have a high degree of hardness are preferred, and for the preparation of Aleumranate, it is also important that the foam has a high adhesive strength with the surface material. However, the strength, elongation, hardness, and transverse properties of 8E****t are maintained within 10e, and the affinity with the material to be bonded is maintained at tkII! It has been extremely difficult to achieve high adhesion strength and high flammability.

一般にエステμ;l&ウレ!ンフオームは機械的諸性質
は良好でToL Lかもフレームラミネート可能で6多
、複合材料の離燃化も容重であるが、高価で番伽、ms
老化し中すい欠点を有する。一方安価なエーテμllt
?しIンフォームは、熱分解時の揮散ヤ残瞭生成など挙
動の差によ勢フレームラPlast 、 JulJ 1
968 、 P276 ) 、特に近時益々要求されて
来九雌燃性をフオームに付与すればする程、益々ファグ
リツタなど他の素材との接着性は低下するのが昔遥であ
る。この丸め安価で温熱老化に強いエーテル系ウレIン
フォームをフレームフ電車−計可能にする為の研究がな
されているが、未だ不十分である。
In general, esthetics μ;l & ure! The foam has good mechanical properties, can be flame laminated with ToL and L, and is also effective in making composite materials flammable, but it is expensive, expensive, and ms.
It has the disadvantage of aging easily. On the other hand, cheap Aete μllt
? The information is based on the difference in behavior such as the formation of volatilization and residue during thermal decomposition.
968, P276), it has long been the case that the more flammability that is given to a foam, which has been increasingly required in recent years, the more its adhesiveness with other materials such as fag ivy deteriorates. Research has been carried out to make this ether-based urethane foam, which is inexpensive and resistant to thermal aging, suitable for frame rolling, but it is still insufficient.

例、tば、エーテ14/−りvIフンォームをフレーム
ラ蝿ネート可能とする方法として、VオールとIダマ−
ポリオ−〜を使用する亀の(#公明56−4022! 
)がある、この方法の関層点としては、lリマーがψオ
ーに使用によるスコーチングがある。
For example, as a method of making it possible to frame the VI form,
Turtle using polio (#Komei 56-4022!
), and a related point of this method is scorching due to the use of lrimer on ψo.

を九、離燃性も十分でない。9. Flammability is also insufficient.

本願発明者らは長年研究の結果、機械的諸性質。The inventors of this application have developed various mechanical properties as a result of many years of research.

温熱老化性に優れ、十分な離燃性を付与され、しかもフ
ミネーVMン裏品を形成する素材との接着強度の大きい
フレームラミネーシ厘ン可能なエーテμ系軟質つレタン
フォー五の婁造に成功したものであって、その要曾とす
る所は、有機イyvアネートと/lエーテ〃Iツオーβ
を小量の発泡剤、触媒、整泡剤の存在下で発泡重合させ
て軟質XIIFIりMlフンォームをJIl?aするに
際し、A、使用するI9エーテ/&/dI9オー〃の分
子量がヒドロキl/A/基Ill当$a〜2000であ
〉、B、主として用vhるポ響エーテμポリオ−〃は実
質的Ks富能を有し、これに4官能以上の多官能基を有
する11エーテβl響オールを全I蓼オーμ重量に対し
10〜40%含有せしめ、C1金19オ一β重量の1〜
20重量優のイツVア車−ト基と反応するリン訃よび/
ま九は八−ゲνを含有する反応層難燃剤を用い、 D、フオーム重量に対するψν分が妬〜楊重量優でhす
、八−グン分が塩素換算でリン分の釦〜細倍量となるよ
う、イyrアネートと実質的に度広し1にい添加WII
燃剤を併用せしめる事を特徴とするフレームヲミネーF
ilン可能な軟質l蓼つレタンフオームの側進方法に関
するものである。
Succeeded in creating a soft urethane material that has excellent thermal aging properties, has sufficient flammability, and can be used for flame lamination with the material that forms the FUMINE VM backing. The essence of this is that organic yv annate and /l ether β
is foamed and polymerized in the presence of a small amount of blowing agent, catalyst, and foam stabilizer to produce a soft XIIFI foam. A, the molecular weight of the I9ether/&/dI9O to be used is $a~2000 per hydroxyl/A/group Ill, and B, the polyether μpolyio to be mainly used is substantially 10 to 40% of the total weight of C1 gold and 19 to 100% of the weight of C1 gold and
Phosphorous group reacting with 20% V-carto group and/
For the first time, a reaction layer flame retardant containing 8-gev is used, D, the ψν component relative to the foam weight is excellent, and the 8-gun component is the phosphorus content in terms of chlorine. Addition WII is substantially increased to 1% with iyranate so that
Frame Omine F characterized by the combination of fuel
The present invention relates to a method for laterally advancing a flexible leash form that can be injected.

本発明に便用畜れるdlオー*、II燃剤以外の成分、
すなわち、lリイyvアネート、ia#IM。
Ingredients other than dlO *, II refueling agent, which can be used in the present invention,
That is, lliyvanato, ia#IM.

麺線および助剤類については、いずれも軟質ウレタンフ
オームを得る為の公知の4のでよ−。
Regarding the noodle strings and auxiliary agents, there are four known methods for obtaining soft urethane foam.

本発QliK使用される19エーテ/&/dリオーβと
しては、実質的に6個以上の活性水素含有化金物に、ヱ
ナVンオ等Vド、ブリピレンオキシドなどを単独付加1
1九は2種以上をフンダムもしくはブロック付加し丸形
のポ菅エーテβ/9オー〃があげられ、実質的に6官能
である生えるポ響エーテμポ9オー〃の分子量はヒドー
キviv基1個当ヤ30O〜2000が好盲しく、例え
ば〆t・ケミカル社で販売しティるホラi −J&/5
140.6022.47011どがそれらのポ譬オー〃
として使用可能である。゛4個域上の富能基を有するI
lオーβとしては、エナレシVアミン、Vエチレントリ
アミン、ペンタ工lス曽トー〜、y14/ピトー〃、V
ユークーーズなどにエチレンオキナイドブ−−ピレンオ
キすイドなどを単独付加t&は、フンダムもしくはブロ
ック付加しえものがあげられる。これらの化金物の分子
量はヒドロキV〜基1優尚Da〜20013が好まし−
0例えば、住友パイエβウレフンの5BTJdツオー*
OJ$41は6富能て、ヒトVキvst基1備14伽約
1870の分子量を持ってsP勢、使用可能である。多
宵簡ダーオーβは、剥離強さを増加する丸めのがオー*
*を使用する際の硬度低下を補う目的で使用される。大
量の多富能dIダオー〜の使用は、剥離強さの低下、難
燃性の低下をもたらす為、金I9オーJhIl量の10
〜40%の使用が好ましい。
The 19ether/&/dlioh β used in the present QliK is obtained by adding Vd, bupyrene oxide, etc. to substantially six or more active hydrogen-containing metal compounds.
19 is a round-shaped po-suga-ete β/9-oh which is obtained by adding two or more types of phyto-ethers or blocks. If the individual winning price is 300~2000, for example, the Hora i-J&/5 sold by T・Chemical Co., Ltd.
140.6022.47011 What are those poems?
It can be used as゛I with enriched functional groups over 4 regions
Examples of l-o-β include Enareshi V amine, V ethylene triamine, Pentachloride, Y14/Pito, and V
Ethylene oxide, pyrene oxide, etc. can be added to Eucouse etc., and t& may be added to Fundum or block. The molecular weight of these metal compounds is preferably hydroxy V to group 1 Da to 20013.
0 For example, Sumitomo Payet β Urefun's 5BTJd Tsuo *
OJ$41 has a molecular weight of about 1870 and has a molecular weight of about 1870 with 1 human V-st group and can be used as an sP. Tayokan Dau β is rounded to increase peel strength.
*It is used to compensate for the decrease in hardness when using. The use of a large amount of multi-enriched dI dao causes a decrease in peel strength and flame retardancy.
Use of ~40% is preferred.

イソVアネート基と反応する反応璽離燃剤としては、例
えば、ファイー−pv6 (ス)ウファ−)、t −e
 l y R?−2jS6 (オーリン)、78514
 (’ワイアyyy))、工XOLMIGO%B251
 (SOI、WAY )モジくはジプロ峨ネオベンチル
ダvex−A/及びそれのエピターHEド響ン付加体で
あるDBNPG。
Examples of the reactive flame release agent that reacts with the isoV anate group include phi-pv6(s)ufa-), t-e
ly R? -2jS6 (Olin), 78514
('waiayyyy)), engineering XOLMIGO%B251
(SOI, WAY) Modifications include DBNPG, which is dipro-neobentilda vex-A/ and its epiter HE doson adduct.

IFD−151、EPD−201、gPD−401(長
瀬麿業)。
IFD-151, EPD-201, gPD-401 (Maro Nagase).

Jlll化ビスツエノーyA1tびその一導体など2盲
簡の反thll!難燃剤が好ましい。
Jlll biszeno yA1t and its one conductor etc. 2 blind letters anti-thll! Flame retardants are preferred.

一般に軟質9し!ンフォームと被接着素材との接着強度
を大にする丸めに、分子量の会艶大きく1に+/%ジオ
ーμの使用が考えられるが、これの多用は%fh九ずら
に離燃性及び圧縮永久giK悪影響を与え、を九難燃剤
の多用は接着強度を低下せしめるので、本質的に雌燃基
を分子中に有するジオ−μの適量の使用が必要となる。
Generally soft 9! In order to increase the adhesive strength between the foam and the material to be bonded, it is possible to use +/% Geoμ, which has a molecular weight of 1 +/%, but the heavy use of this increases the flammability and compressibility of %fH9. Since heavy use of flame retardants can adversely affect permanent GIK and reduce adhesive strength, it is necessary to use an appropriate amount of Geo-μ, which essentially has a female flammable group in the molecule.

丸だし、過剰の使用は、ターーズセ〜のフオームを生じ
、圧縮残留量が悪くなる。使用量としては、全ボ響オー
ρ重量Kjtして1〜20令が好ましい。
If rounded or used in excess, a turquoise foam will result, and the amount of compression remaining will be poor. The amount to be used is preferably 1 to 20 years in terms of total volume weight Kjt.

イyyアネート基と実質的に反応しない添加1雌燃剤と
しては、第四申ス傘二tム化合物、有機リン酸塩、有機
態リン酸塩、有機傘スホネート。
Examples of additive fuel agents that do not substantially react with the yyanate group include quaternary compound, organic phosphate, organic phosphate, and organic sulfonate.

會へ騨ゲン9ン酸エステル、へロゲン化物ナトカある0
例えに、會へロゲグーエステルとしては、TOIP、0
RP(大入化学)、ホスI−ドC−22−R%傘x f
−)’ZXO−20(*ンt ン) )、:  ・8に ファイロー477(スト9フアーケミカβ) 、0R−
505、OR41M  (大入化学)、CP−4Q口(
三井東圧ファイン)、f−モ曽ン101(オーリン)ナ
トが使用可能である。へpゲン化物としてはROMに1
.0R50(日麿フェロ有機化学)などがある、他に縮
合リン酸アンモニウムも使用IU能であり、スミ竜−フ
P、ス電セーフPM(住友化宇>−fi’14J用でき
る。
There are 9-phosphate esters and helogenides in the meeting.
For example, as a logegooester to the meeting, TOIP, 0
RP (Oiri Kagaku), Phos I-do C-22-R% umbrella x f
-)'ZXO-20 (*nt n) ),: ・Fylow 477 (St9 Far Chemica β) at 8, 0R-
505, OR41M (Oiritsu Chemical), CP-4Q mouth (
Mitsui Toatsu Fine) and f-Moson 101 (Orlin) Nat can be used. As a hepgenide, 1 is in ROM.
.. In addition, condensed ammonium phosphates such as 0R50 (Nimmaro Ferro Organic Chemical Co., Ltd.) can also be used for IU, and can be used for Sumiryu-F P and Suden Safe PM (Sumitomo Chemical Fi'14J).

これらの添加ma*m剤を使用する目的は、反応層難燃
剤との組会わせK)いて、フォー五重量に対してリンが
帖〜1S%、ハロゲン分は複素換算で9ンのu〜団倍量
を確保するえめであや、かくしてリン、八−ゲン比率中
難燃剤しベ〃を最適にする処方を組み立て為ことが出来
るのである。
The purpose of using these additive ma*m agents is to combine them with the flame retardant in the reaction layer.The phosphorus content is ~1S% and the halogen content is 9~9% by weight based on the weight of the flame retardant. By ensuring the amount of compounding, it is thus possible to create a formulation that optimizes the phosphorus, octogen ratio, flame retardant and base.

以下実施例について述べる。Examples will be described below.

実施例に使用した原料 ポラノーμ6140   ダウケミカμOH価45.6
富− 8BU#lオー#0541  住友パイエμウレフン 
OH@5O16富能 NIAX  A−I    U、’O,C。
Raw materials used in the examples Polanor μ6140 Dow Chemica μOH value 45.6
Wealth - 8BU #l O #0541 Sumitomo Payer μ Urehun
OH@5O16 Funo NIAX A-I U,'O,C.

DMIA        日本乳化剤 Vメチル工!ノー〃アミン F −450信越Vリコン v9コン界面活性剤 I P D −401長鋼産業 Vプーモネオベンチ〜グリスールのエピター〃とド曽ン
4モp付加物、複素25優、臭素28%、OH価97 KPD−4Ql      長瀬麿東 Vブロモネオベンチμグリコ−μのエピタ費fi/ヒト
リン!璧β付加物、複素16優、臭素66g6、OH価
250 サー篭りン101・    オー9ン リン1五14、複素5(Ll % ファイ費−〜77     スト9フアーV ン1A4
*、m素2ZO* c p −6oo       三井東圧フアミンリ 
 ν 12s % 、  複素 2ξI5 %使用し九
布地 布地1 素材:ナイ四ン/−讐エステ〃繊維、起毛ニット 離燃処理二69 布地2    〜 素材:I−エステル繊Il m物 400 f4iIl
雌maw  i。
DMIA Nippon Emulsifier V Methyl Engineering! No Amine F-450 Shin-Etsu V Recon V9 Con Surfactant I P D-401 Long Steel Sangyo V Pumone Bench ~ Glysol Epiter and Doson 4 Mop Adduct, Complex 25, Bromine 28%, OH Value 97 KPD-4Ql Nagase Maro V Bromone Bench μ Glyco-μ Epitacost fi/Hitrin! β-adduct, complex 16, bromine 66g6, OH number 250, 101, 9, 15, 14, complex 5 (Ll % Phi cost - ~ 77, 9 fa-V, 1A4)
*, m element 2ZO* c p -6oo Mitsui Toatsu Fuminri
ν 12s %, complex 2ξI5% 9 fabrics Fabric 1 Material: Ni-4/-Este fiber, brushed knit flame release treatment 269 Fabric 2 ~ Material: I-ester fiber Il m material 400 f4iIl
Female maw i.

布地6 素材:rygエステ〜繊― 細物 480ルW雌燃処珈
:h餠 試論方法 1Fffi:       、TISt64Qlam、
254II、D :  :JISKls481遥気性:
      ASTMD1564(ofpmを漕に換算
) so優圧縮畳:   J工Sに64o1伸び率:   
  J工5K4402 引me強−11:    ;f工5K4402引裂き憤
さ:    、yxsic44g211111II強さ
:     、yxsL1064am試験:     
JI!iD12g1発   泡 l譬オール成分j$o@ fを使用し、イソシアネート
以外の他の成分を秤量し% 1700r、p、mのミキ
賃−で20秒問プレミックスを行う、25υKm調後、
25tK温調し九イソVア卓−トを必要量添加し、直ち
に7秒1161%しテ270x270x250sgoM
泡11中に注ぎ、オープン発泡させる。
Fabric 6 Material: Ryg Esthetics ~ Textile - Thin 480 ru W female combustion fabric: H 餠 Trial Method 1Fffi: , TISt64Qlam,
254II, D: :JISKls481 Harukei:
ASTM D1564 (converting ofpm to rows) So-yu compression tatami: 64o1 elongation rate for J-K S:
J engineering 5K4402 tear strength -11:;
JI! Using iD12g1 foaming l all component j$o@f, weigh other components other than isocyanate and perform premixing for 20 seconds at a mixing rate of 1700r, p, m, after adjusting for 25υKm.
Adjust the temperature at 25tK, add the necessary amount of Nineiso V atrate, and immediately boil it to 1161% for 7 seconds.
Pour into foam 11 and allow to open and foam.

このようにして得られたフォー五について物性試験とフ
レームヲミネーシ舗ン性のテストを打つ九。
The four pieces obtained in this way were subjected to physical property tests and frame finishing tests.

7V−ムラ鳳ネーVMンの方法 厚さ12麿、長さ650厘、巾115麿のウレタンフオ
ーム片をと抄、巾110■、高さ70厘に調整され九I
、Pfスの火炎上(バーナーの口の上40厘)を1s峠
のスピードで通過させて表面を熔融させる。
7V-Unevenness Method A piece of urethane foam with a thickness of 12 mm, a length of 650 mm, and a width of 115 mm was cut and adjusted to a width of 110 mm and a height of 70 mm.
, a flame of Pf gas (40 mm above the mouth of the burner) is passed through at a speed of 1 second to melt the surface.

直ちに布地と重ね合せ、バーナーから90■離れ九所に
位置する閃原4M1f)ローρを通して8E着し友。
Immediately overlap it with the fabric and attach it to Senhara 4M1f) located 90cm away from the burner and 8E through low rho.

圧着後124 F/−の荷重をかけて一鳳夜放置後、剥
離強さとmsmテスト用のすンプβとした。
After crimping, a load of 124 F/- was applied and the sample was left overnight for peel strength and sump β for msm tests.

第1表は各実施例の獣舎を示し、第2表は各実施例の試
験結果を示す。
Table 1 shows the animal housing for each example, and Table 2 shows the test results for each example.

実施例での効果 第1褒棗び第211に示すようK、本発11QKよる軟
質?&/Iシフオームは、発泡体としての機械的諸性能
が水準に違しえものであるのはもちろんのこと、これに
よるフレーム9電ネーvWy製品は十分tsi燃性能を
有しながら、大きな接着強度を持ち、本発明の効果は明
らかである。
Effect in the example As shown in the first reward No. 211, K is soft due to the main 11 QK? &/I Siform not only has the mechanical performance of a foam that is on par with other standards, but the Frame 9 Electric NevWy product made from it has sufficient TSI flame performance and has great adhesive strength. The effect of the present invention is obvious.

特許出願人 井上エムチーピー株式会社手  続  補
  正  書 昭和56年9万14日 特許庁長音 島 1)審 樹  殿 1、事件の表示  昭和56年特許願第118119号
2 発明の名称 フレームラミネーVWン可能な難燃性軟質ポリウレタン
フォームの製造方法 己 補正をする者 事件との関係 特許出願人 住所 名古屋市中村区名駅南二丁目16番4号(〒45
0)瓜 補正の内容 (1)  明細書第7頁第1′6行日から第14行ti
KrB251(SOI、VAT)4しくlとあるを、「
B251(SOLVAY)、液状paafvンFH−0
50(電気化学)もしくは」と補正します。
Patent Applicant: Inoue MCHIP Co., Ltd. Procedural Amendment Written by the Director of the Japan Patent Office, dated 90,141, 1982, Otojima 1) Trial Judge: 1, Indication of the case: 1981 Patent Application No. 118119 2 Name of the invention: Frame lamination VW possible Method for producing flame-retardant flexible polyurethane foam Relationship with the case of the person making the amendment Patent applicant address 2-16-4 Meiekiminami, Nakamura-ku, Nagoya (45
0) Melon Contents of the amendment (1) Page 7 of the specification, line 1'6 from date to line 14 ti
KrB251 (SOI, VAT) 4.
B251 (SOLVAY), liquid paafvn FH-0
50 (electrochemistry) or''.

(2)II811IG15行目K r傘Xf−)’ZX
C!−20Jとあるを、「ホスガード2XO−20Jと
補正します。
(2) II811IG 15th line K r umbrella Xf-)'ZX
C! -20J will be corrected to "Hosgard 2XO-20J.

(3)  第8頁第19行目から第20行目にl”RO
MKLOR50J と6At、rBROMKLOR50
Jと補正し★す。
(3) l”RO on page 8, line 19 to line 20
MKLOR50J and 6At, rBROMKLOR50
Correct it with J★.

以   上that's all

Claims (1)

【特許請求の範囲】 有機イソシアネートとlリエーテ〃I菅オー〜を小量の
発泡剤、触媒、整泡剤の存在下で発泡重金させて軟質1
19しIンフォームを製造するに際し、 ム、使用するぽ響エーテμm蓼オーβの分子量が1e、
ドaqVpt基1個当知zoo 〜zoooであり、B
、主として用いる1wエーテwdリオールは実質的に墨
富龍を有し、これに4官能以上の多實龍基を有するII
IWエーテJI/4iリオ−声を金ポリオー〃重愈に対
し10〜4gI%會有せしめ、0、金/9オー*l量(
F) 1−40簾量優のイysty卓−ト基と度広する
蓼ν)よび/會えはハーゲンを含有する反応履難燦剤を
使用し、 D、フオーム重量に対するψン分がら〜楊重量優であ艶
、へ賛ゲン分が塩素換算でダン分の勾〜閘倍量となる橡
、インシア車−ト基と実質的に反応しない添加層難燃剤
を併用せしめる 事を特徴とするフレームラミ車−シ纏ン可能な難燃性軟
質−9ウレIンフォームの製造方法。
[Claims] An organic isocyanate and a liate are foamed in the presence of a small amount of a blowing agent, a catalyst, and a foam stabilizer to form a soft one.
19 When producing I-form, the molecular weight of the Pokyo Aete μm-O β used is 1e,
One aqVpt group is known from zoo to zooo, and B
, the 1W ether wd Riol mainly used has substantially Sumitomo Ryu, and II which has a multi-functional Ryu group of 4 or more functional groups.
IW Aete JI/4i Rio-Voice with 10 to 4gI% to gold polio heavy, 0, gold/9oh*l amount (
F) 1-40 ysty table group and widening base ν) and/or using a reaction retardant containing Hagen; It is characterized by the combination of an additive layer flame retardant that does not substantially react with the chlorine and insea carton groups, which has a high gloss and high luster, and whose heat content is the same as the Dan content in terms of chlorine. Frame laminated wheel - method for producing flame-retardant flexible 9-urethane foam that can be wrapped.
JP56118119A 1981-07-28 1981-07-28 Production of flame-laminatable, flame-resistant soft polyurethane foam Pending JPS5819321A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56118119A JPS5819321A (en) 1981-07-28 1981-07-28 Production of flame-laminatable, flame-resistant soft polyurethane foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56118119A JPS5819321A (en) 1981-07-28 1981-07-28 Production of flame-laminatable, flame-resistant soft polyurethane foam

Publications (1)

Publication Number Publication Date
JPS5819321A true JPS5819321A (en) 1983-02-04

Family

ID=14728496

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56118119A Pending JPS5819321A (en) 1981-07-28 1981-07-28 Production of flame-laminatable, flame-resistant soft polyurethane foam

Country Status (1)

Country Link
JP (1) JPS5819321A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61141722A (en) * 1984-12-14 1986-06-28 Achilles Corp Production of flame-laminatable, flame-retarding flexible polyurethane foam
JPS61157515A (en) * 1984-12-28 1986-07-17 Achilles Corp Production of flame-retardant polyurethane foam bondable by flame lamination
US4880844A (en) * 1988-05-27 1989-11-14 Akzo America Inc. Flame laminatable polyether urethane foam
JPH0261638U (en) * 1988-10-31 1990-05-08
US8535476B2 (en) 2007-08-01 2013-09-17 Dow Global Technologies Llc Heat bonding polyurethane foams
KR20140143429A (en) * 2012-03-30 2014-12-16 에어 프로덕츠 앤드 케미칼스, 인코오포레이티드 Polyurethane foam production process, pre-mix, formulation, and product

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4847992A (en) * 1971-10-21 1973-07-07

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4847992A (en) * 1971-10-21 1973-07-07

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61141722A (en) * 1984-12-14 1986-06-28 Achilles Corp Production of flame-laminatable, flame-retarding flexible polyurethane foam
JPH0579688B2 (en) * 1984-12-14 1993-11-04 Achilles Corp
JPS61157515A (en) * 1984-12-28 1986-07-17 Achilles Corp Production of flame-retardant polyurethane foam bondable by flame lamination
US4880844A (en) * 1988-05-27 1989-11-14 Akzo America Inc. Flame laminatable polyether urethane foam
JPH0261638U (en) * 1988-10-31 1990-05-08
JPH0546893Y2 (en) * 1988-10-31 1993-12-09
US8535476B2 (en) 2007-08-01 2013-09-17 Dow Global Technologies Llc Heat bonding polyurethane foams
KR20140143429A (en) * 2012-03-30 2014-12-16 에어 프로덕츠 앤드 케미칼스, 인코오포레이티드 Polyurethane foam production process, pre-mix, formulation, and product
JP2015512988A (en) * 2012-03-30 2015-04-30 エア プロダクツ アンド ケミカルズ インコーポレイテッドAir Products And Chemicals Incorporated Polyurethane foam manufacturing method, premix, blend and product

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