JPS6213426A - Production of coarse-cellular flexible urethane foam - Google Patents

Production of coarse-cellular flexible urethane foam

Info

Publication number
JPS6213426A
JPS6213426A JP60152858A JP15285885A JPS6213426A JP S6213426 A JPS6213426 A JP S6213426A JP 60152858 A JP60152858 A JP 60152858A JP 15285885 A JP15285885 A JP 15285885A JP S6213426 A JPS6213426 A JP S6213426A
Authority
JP
Japan
Prior art keywords
polyol
urethane foam
rotation speed
amount
coarse
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
JP60152858A
Other languages
Japanese (ja)
Inventor
Takashi Nishi
敬 西
Kiyomi Nakamura
清実 中村
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.)
Toyo Tire Corp
Original Assignee
Toyo Tire and Rubber 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 Toyo Tire and Rubber Co Ltd filed Critical Toyo Tire and Rubber Co Ltd
Priority to JP60152858A priority Critical patent/JPS6213426A/en
Publication of JPS6213426A publication Critical patent/JPS6213426A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the title urethane foam which is beautiful and has coarse cells, by reacting a polyol component with a polyisocyanate component under conditions including a specified rotation speed of the rotating impellers of a mixing head and a specified amount of a catalyst. CONSTITUTION:A mixture (A) of an at least bifunctional OH group-containing polyol component (a) (e.g., polyoxypropylene ether polyol of an OH value of 56) and, preferably, bi- to tetrafunctional polyol of a MW of 300-1,000 (e.g., diol) is reacted with an at least bifunctional polyisocyanate (e.g., tolylene diisocyanate) in the presence of a urethane formation catalyst (e.g., triethylenediamine) in an amount about 1.2-3 times that usually used by running the rotating impellers of a mixing head at a rotation speed of about 400-2,000rpm.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は粗大気泡を有する軟質ウレタンフオームの製造
方法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for producing a flexible urethane foam having coarse cells.

(従来の技術) 軟質ウレタンフオームを作る場合、通常の軟質7オーム
用3官能性ポリオール、ポリイソシアネート、触媒、発
泡剤、その他添加剤を使用している。一般に軟質ウレタ
ンフオームの製造におけるミキシングヘッドの回転羽根
の回転数は4000〜6000 r +1+aであり、
この場合には2.54cm当り約40個以上の細かいセ
ルを有した7オームが得られる。
(Prior Art) When making a flexible urethane foam, conventional trifunctional polyols for flexible 7 ohms, polyisocyanates, catalysts, blowing agents, and other additives are used. Generally, the rotation speed of the rotating blade of the mixing head in the production of soft urethane foam is 4000 to 6000 r +1 + a,
In this case, 7 ohms with about 40 or more fine cells per 2.54 cm are obtained.

回転数を増加すると更に細かい気泡の7オームが得られ
、逆に回転数を小さくするとセルは粗くなる。しかし回
転数を小さくすると薬液同士の接触が少なくなり、内部
ブロクや7オームの周囲が未反応物の発生によりボロボ
ロとなり満足できる製品は得られない。
If the rotation speed is increased, finer cells of 7 ohms can be obtained, and conversely, if the rotation speed is decreased, the cells become coarser. However, when the rotational speed is reduced, contact between the chemical solutions decreases, and the internal block and the surrounding area of the 7 ohm become tattered due to the generation of unreacted substances, making it impossible to obtain a satisfactory product.

(発明が解決しようとする問題点) 本発明の目的は満足できる製品形態、性能を有し、且つ
粗いセルを有する粗泡性軟質ウレタンフオームの製造方
法を提供することにある。
(Problems to be Solved by the Invention) An object of the present invention is to provide a method for producing a coarse flexible urethane foam having satisfactory product form and performance and having coarse cells.

(問題点を解決するための手段) 本発明は少なくとも2官能性の水酸基を有するポリオー
ル成分と、少なくとも2官能性のポリイソシアネート成
分を反応させる軟質ポリウレタンフォームの製造方法に
おいて、ミキシングヘッドの回転羽根の回転数を約40
0〜2000rpmに下げ、且つウレタン化触媒の使用
量を通常の使用量の約1.2〜3倍量に高めたことを特
徴とする粗泡性軟質ウレタンフオームの製造方法に係る
(Means for Solving the Problems) The present invention provides a method for producing flexible polyurethane foam in which a polyol component having at least difunctional hydroxyl groups and an at least difunctional polyisocyanate component are reacted. The number of revolutions is about 40
The present invention relates to a method for producing a coarsely foamable flexible urethane foam, which is characterized in that the speed is lowered to 0 to 2000 rpm, and the amount of urethanization catalyst used is increased to about 1.2 to 3 times the amount normally used.

本発明で使用されるポリオール成分としては公知の軟質
7オーム用3官能性ポリオールを挙げることができる。
Examples of the polyol component used in the present invention include known soft trifunctional polyols for 7 ohms.

この上うな3官能性ポリオールとしては、公知の水酸基
価(以下OH価という)35〜65の範囲のポリエステ
ルポリオール、ポリニー噂1 チルポリオールはすべて使用可能であるが、特に08価
56のポリオキシプロピレンエーテルポリオール又はポ
リオキシエチレンプロピレンエーテルポリオールが好ま
しい。
In addition, as trifunctional polyols, all known polyester polyols with a hydroxyl value (hereinafter referred to as OH value) in the range of 35 to 65 and polynylene polyols can be used, but in particular, polyoxypropylene with a hydroxyl value of 56 to 08 can be used. Ether polyols or polyoxyethylene propylene ether polyols are preferred.

本発明で使用されるポリイソシアネート成分としては、
公知の少くとも2官能性のポリイソシアネートはすべて
用いることができるが、特に芳香族ポリイソシアネート
が好適で、例えば2,4−及び2.6−)リレンジイソ
シアネー)(TDI)、オルトトルイノンノイソシアネ
ー)(TODI)、ナ7チレンジイソシアネー)(ND
I)、キシリレンジイソシアネート(MDI)、4,4
′−ジフェニルメタンジイソシアネー) (MD I 
)及びカーポジイミド変性MDI(例えば日本ポリウレ
タン社MTL)、ポリメチレンボリフェニルイソシアネ
ー)(PApH、ポリメリックポリイソシアネート(例
えば住人バイエルウレタン44■)等を単独又は併用し
て使用することができる。
The polyisocyanate component used in the present invention includes:
All known at least difunctional polyisocyanates can be used, but aromatic polyisocyanates are particularly preferred, such as 2,4- and 2,6-)lylene diisocyanate (TDI), orthotoluinone isocyanate) (TODI), sodium chloride diisocyanate) (ND
I), xylylene diisocyanate (MDI), 4,4
'-diphenylmethane diisocyanate) (MD I
), carposiimide-modified MDI (for example, Nippon Polyurethane Co., Ltd. MTL), polymethylene polyphenylisocyanate (PApH), polymeric polyisocyanate (for example, Sumitomo Bayer Urethane 44), etc. can be used alone or in combination.

本発明ではウレタンフオームの製造時、薬液のミキシン
グヘッドの回転羽根の回転数を約400〜2000rp
mと通常の回転数より逼かに小さくし、且つウレタン化
触媒の使用量を通常の回転数の場合の使用量の約1.2
〜3倍量に高めることを特徴とする。これにより、きれ
いな7オームでセルのみが粗い目的とする7オームが得
られる。触媒としては公知のウレタン化触媒を用いるこ
とができ、例えばT−9〔吉富製薬製、錫触媒〕、トリ
エチレンジアミン〔7−ドリー社製、アミン系触媒、ダ
プコ〕などを代表例とする錫触媒、アミン系触媒、その
他の触媒を使用することができる。触媒量が1.2倍未
満では7オームは不完全であり、3倍を越すと7オーム
は収縮しやすくなる。
In the present invention, when manufacturing urethane foam, the rotation speed of the rotating blade of the chemical mixing head is set at approximately 400 to 2000 rpm.
m is much smaller than the normal rotation speed, and the amount of urethanization catalyst used is about 1.2 of the amount used at the normal rotation speed.
It is characterized by increasing the amount by ~3 times. This will give you the desired 7 ohms with a clean 7 ohm and only a rough cell. As a catalyst, a known urethanization catalyst can be used, such as a tin catalyst such as T-9 (manufactured by Yoshitomi Pharmaceutical Co., Ltd., tin catalyst), triethylenediamine (manufactured by 7-Dolly Co., Ltd., amine catalyst, Dapco), etc. , amine catalysts, and other catalysts can be used. If the amount of catalyst is less than 1.2 times, 7 ohm is incomplete, and if it exceeds 3 times, 7 ohm tends to shrink.

本発明では上記回転羽根の回転数と触媒量のバランスに
加えて、分子量(MW)が300〜1000で2〜4官
能のポリオールを上記ポリオール成分に併用すると更に
完全な7オームが得られ好ましい。
In the present invention, in addition to the balance between the rotational speed of the rotating blade and the amount of catalyst, it is preferable to use a bifunctional to tetrafunctional polyol with a molecular weight (MW) of 300 to 1000 in combination with the polyol component to obtain a more perfect 7 ohm.

このようなポリオールとしてはジオール、ポリオール、
ビス7エ/−ルAのPO付加物、芳香族アミン基体ポリ
オールなどが挙げられ、市販品では例えばBISQL−
2P[東邦千葉化学製、ビスフェノールAのPO(プロ
ピレンオキサイド)付加物〕、GR−30[代用薬品製
、芳香族アミン基体ポリオール]、D ial 200
0 (旭電化製、ジオール、MW2000)、K S 
570 (第−工業製薬製、M W 400゜OH価5
70〕などを例示できる。
Such polyols include diols, polyols,
Examples include PO adducts of Bis7el/-A, aromatic amine-based polyols, and commercially available products include, for example, BISQL-
2P [manufactured by Toho Chiba Chemical, PO (propylene oxide) adduct of bisphenol A], GR-30 [manufactured by Substitute Yakuhin, aromatic amine-based polyol], Dial 200
0 (manufactured by Asahi Denka, Diol, MW2000), K S
570 (manufactured by Dai-Kogyo Seiyaku, M W 400° OH value 5
70], etc.

本発明において前記軟質7オーム用3官能性ポリオール
と上記MW300〜1000のポリオールの使用割合は
前者の90〜99部(重量部、以下同様)に対して後者
の1〜10部とするのが好ましい。
In the present invention, the ratio of the soft 7-ohm trifunctional polyol and the polyol with a MW of 300 to 1000 is preferably 90 to 99 parts (parts by weight, hereinafter the same) of the former and 1 to 10 parts of the latter. .

本発明において、ポリオール類とインシアネート類等と
を反応させてウレタンフオームを作る場合、イソシアネ
ートインデックスは103〜130が望ましいが、所望
の物理特性にもとづいて適宜増減することができる。
In the present invention, when making a urethane foam by reacting polyols with incyanates, etc., the isocyanate index is preferably 103 to 130, but can be increased or decreased as appropriate based on desired physical properties.

又本発明は軟質スラブ7オームのみならずモールド7オ
ームにも適用が可能である。
Further, the present invention can be applied not only to a 7 ohm soft slab but also to a 7 ohm mold.

更に、本発明においては軟質ポリウレタン7オ−ムを製
造するために発泡M、整泡剤が、又必要に応じ難燃剤、
顔料、充填剤等が用いられるが、これらには待に制約が
なく公知のものはすべて使用可能である。
Furthermore, in the present invention, in order to produce flexible polyurethane 7 ohm, foaming M and a foam stabilizer are added, and if necessary, a flame retardant,
Pigments, fillers, etc. are used, but there are no restrictions and all known ones can be used.

(実 施 例) 以下参考例及び実施例に基づき具体的に説明する。(Example) A detailed explanation will be given below based on reference examples and examples.

参考例I P P G 3000 [三井日曹製、3官能性ポリプ
ロピレンポリオール、08価5631000gを2リツ
トルのビーカーにとり、T−9〔吉富製薬製錫触媒〕1
.3g及び整泡剤〔トーレ シリコン製、S H190
)10gを添加し10分間撹拌したものをA液とする。
Reference Example I PPG 3000 [manufactured by Mitsui Nisso, trifunctional polypropylene polyol, 5631000 g of 08 valence] was placed in a 2 liter beaker, and T-9 [tin catalyst manufactured by Yoshitomi Pharmaceutical] 1
.. 3g and foam stabilizer [Made by Toray Silicone, S H190
) 10g was added and stirred for 10 minutes, which is called Solution A.

別に100ccのビーカーに水39.をとり、NMM〔
日本乳化創製、N−メチルモルホリン) 5.Og及び
トリエチレンジアミン〔7−ドリー社製、ダブコ) 0
.5gを添加し撹拌したものをB液とする。
A separate 100cc beaker with water 39. Take NMM [
Nippon Nyukasou, N-methylmorpholine) 5. Og and triethylenediamine [manufactured by 7-Dolly, Dabco] 0
.. 5g was added and stirred, and this was designated as Solution B.

500ccのビーカーにA液を202.26gとり、次
いでB液8.9gを加え、撹拌しながら25°Cに調節
する。
Place 202.26 g of liquid A in a 500 cc beaker, then add 8.9 g of liquid B, and adjust the temperature to 25°C while stirring.

一方TDIを別のビーカーに106gとり22℃に調節
する。A、Bの混合液を回転子によ’) 1500rp
mで10秒攪拌し、そこへ上記TDTを加え、6秒撹拌
後、240 X 240 X 200+*mのオープン
モールドに入れ、これを100℃の乾燥機中に10分入
れて発泡させた。
On the other hand, take 106 g of TDI in another beaker and adjust the temperature to 22°C. Pass the mixture of A and B through the rotor') 1500 rpm
After stirring for 10 seconds at m, the above TDT was added thereto, and after stirring for 6 seconds, the mixture was placed in a 240 x 240 x 200+*m open mold, and placed in a dryer at 100°C for 10 minutes to foam.

得られた7オームの7オーム状態は不良で、JIS K
−6402の方法により測定したセル数は約45個/ 
2,54c111であり、細かいセル7オームであった
The resulting 7 ohm condition is defective and JIS K
- The number of cells measured by the method of 6402 is approximately 45/
It was 2.54c111, fine cell 7 ohm.

fjS1表に配合割合を示す。The blending ratio is shown in table fjS1.

実施例1〜3 第1表に示した配合割合及び条件によった以外は参考例
1と同様にして軟質ウレタンフオームを作成した。結果
を同様第1表に示す。
Examples 1 to 3 Soft urethane foams were prepared in the same manner as in Reference Example 1, except that the blending ratios and conditions shown in Table 1 were used. The results are also shown in Table 1.

第   1    表 参考例2 P P G 3000 (950g)を2リツトルのビ
ーカーにとり、T−9(1,3g)及びS I(190
(Loll>を添加し攪拌したものをC液とする。別の
ビーカーにBISQL−2P[東邦千葉化学製、ビスフ
ェノールAのPO付加物、OH価320]20g、 G
R−30(大田薬品製、芳香族アミン基体ポリオール、
08価400 ) 20g及1/’ :/ :t −ル
(旭電化製、OH価56〕60gをとり撹拌したものを
D液とする。
Table 1 Reference Example 2 PPG 3000 (950g) was placed in a 2 liter beaker, T-9 (1.3g) and SI (190
(Loll> is added and stirred, and this is called liquid C. In another beaker, add 20 g of BISQL-2P [manufactured by Toho Chiba Chemical, PO adduct of bisphenol A, OH value 320], G
R-30 (manufactured by Ota Pharmaceutical, aromatic amine-based polyol,
08 value: 400) and 60 g of 1/':/:t-ru (manufactured by Asahi Denka, OH value: 56) were taken and stirred, and this was used as liquid D.

参考例1のB液、上記C,D!及びTDIを用いて各成
分が第2表に記載の割合となるようにして、参考例1と
同様にして軟質ウレタンフオームを作成した。結果を同
様PIIJ2表に示す。
Solution B of Reference Example 1, the above C, D! A soft urethane foam was prepared in the same manner as in Reference Example 1, using TDI and each component in the proportions shown in Table 2. The results are also shown in Table PIIJ2.

実施例4〜6 第2表に示した配合割合及び条件によった以外は参考例
2と同様にして軟質ウレタンフオームを作成した。結果
を同様第2表に示す。
Examples 4 to 6 Soft urethane foams were prepared in the same manner as in Reference Example 2, except that the blending ratios and conditions shown in Table 2 were used. The results are also shown in Table 2.

第2表 (以 上)Table 2 (that's all)

Claims (2)

【特許請求の範囲】[Claims] (1)少なくとも2官能性の水酸基を有するポリオール
成分と、少なくとも2官能性のポリイソシアネート成分
を反応させる軟質ポリウレタンフオームの製造方法にお
いて、ミキシングヘッドの回転羽根の回転数を約400
〜2000rpmに下げ、且つウレタン化触媒の使用量
を通常の使用量の約1.2〜3倍量に高めたことを特徴
とする粗泡性軟質ウレタンフオームの製造方法。
(1) In a method for producing a flexible polyurethane foam in which a polyol component having at least a difunctional hydroxyl group and an at least difunctional polyisocyanate component are reacted, the rotation speed of the rotating blade of the mixing head is set to about 400.
2000 rpm, and the amount of the urethanization catalyst used is increased to about 1.2 to 3 times the usual amount.
(2)ポリオール成分として、更に分子量300〜10
00の2〜4官能のポリオールを併用する特許請求の範
囲第1項記載の製造方法。
(2) As a polyol component, the molecular weight is 300 to 10.
The manufacturing method according to claim 1, in which a di- to tetrafunctional polyol of 0.00 is used in combination.
JP60152858A 1985-07-10 1985-07-10 Production of coarse-cellular flexible urethane foam Pending JPS6213426A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60152858A JPS6213426A (en) 1985-07-10 1985-07-10 Production of coarse-cellular flexible urethane foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60152858A JPS6213426A (en) 1985-07-10 1985-07-10 Production of coarse-cellular flexible urethane foam

Publications (1)

Publication Number Publication Date
JPS6213426A true JPS6213426A (en) 1987-01-22

Family

ID=15549659

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60152858A Pending JPS6213426A (en) 1985-07-10 1985-07-10 Production of coarse-cellular flexible urethane foam

Country Status (1)

Country Link
JP (1) JPS6213426A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013221118A (en) * 2012-04-18 2013-10-28 Dic Corp Two-liquid curable resin composition, coating agent and coating film

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013221118A (en) * 2012-04-18 2013-10-28 Dic Corp Two-liquid curable resin composition, coating agent and coating film

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