Nothing Special   »   [go: up one dir, main page]

JPH05320304A - Production of polyurethane foam for seat cushioning improved in comfortableness to ride - Google Patents

Production of polyurethane foam for seat cushioning improved in comfortableness to ride

Info

Publication number
JPH05320304A
JPH05320304A JP4133551A JP13355192A JPH05320304A JP H05320304 A JPH05320304 A JP H05320304A JP 4133551 A JP4133551 A JP 4133551A JP 13355192 A JP13355192 A JP 13355192A JP H05320304 A JPH05320304 A JP H05320304A
Authority
JP
Japan
Prior art keywords
polyurethane foam
foam
polyol
comfortableness
ride
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
JP4133551A
Other languages
Japanese (ja)
Other versions
JP3279640B2 (en
Inventor
Shigeyoshi Fukushima
繁義 福島
Koji Izumi
孝司 泉
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 JP13355192A priority Critical patent/JP3279640B2/en
Publication of JPH05320304A publication Critical patent/JPH05320304A/en
Application granted granted Critical
Publication of JP3279640B2 publication Critical patent/JP3279640B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6681Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6685Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3225Polyamines
    • C08G18/325Polyamines containing secondary or tertiary amino groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To produce a polyurethane foam for seat cushionings improved in comfortableness to ride by reacting a polyol component containing a specific secondary aromatic amine blended therein with a polyisocyanate component. CONSTITUTION:The polyurethane foam is obtained by reacting (A) a polyol component prepared by blending (A1) 100 pts.wt. polyol such as a bi- to a trivalent polyoxypropylene polyol having preferably 20-65 hydroxyl value with (A2) 0.5-5 pts.wt., preferably 0.5-2.5 pts.wt. secondary aromatic amine of the formula (R and R' are 1-3C alkyl) [e.g. 4,4'-bis-(methylamino-diphenylmethane)], (A3) a catalyst and (A4) a foaming agent (preferably water or its mixture with a small amount of a substitute fluorocarbon added thereto) and, as necessary, other additives blended therein with (B) a polyisocyanate component (e.g. tolylene diisocyanate (TDI) or polymeric cyanate). This polyurethane foam has softness, degrees of sinking and bouncing and characteristics of vibration and comfortableness to ride suitable as seat cushionings.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は乗り心地の改良されたシ
ートクッション用ポリウレタンフォームの製造方法に関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a polyurethane foam for a seat cushion having improved riding comfort.

【0002】[0002]

【従来の技術】近年、自動車産業の発展に伴い、車の機
能性向上はもとより、車輌内装の高級化、居住性の向上
・改善が求められるようになった。そして、特に乗り心
地改良の観点から、クッション特性のより優れた座席用
ポリウレタンフォームの開発が強く望まれている。
2. Description of the Related Art In recent years, along with the development of the automobile industry, not only the functionality of a vehicle has been improved, but also the interior of a vehicle has been upgraded and the comfortability has been improved / improved. In particular, from the viewpoint of improving the riding comfort, there is a strong demand for the development of a polyurethane foam for seats having more excellent cushioning properties.

【0003】座席のクッション特性はシートの乗り心地
を評価する要素の一つであって、その指標となる静的及
び動的特性としては一般に次のような点が指摘されてい
る。 荷重試験でえられるたわみ量が大きい方が良い。但
し、たわみ量が余り大きくなると、尻や腰椎部が沈み過
ぎたり、底付き感が生じ易くなり好ましくない。 静バネ定数が小さい方が良い。特に75%たわみ時の
加圧側曲線の傾きは、底付き感を評価する指標であっ
て、これが小さい方が良い。 振動試験でえられる共振振動周波数および振動伝達率
が小さい方が良い。即ち、振動乗り心地の8割りはシー
トを介して伝えられる振動であり、これらシートの伝達
特性の改善は乗り心地の改良にとって重要な因子とされ
ている。
The cushion characteristic of the seat is one of the factors for evaluating the riding comfort of the seat, and the following points are generally pointed out as the static and dynamic characteristics that are the indexes. The larger the amount of deflection obtained by the load test, the better. However, if the amount of deflection is too large, the hips and lumbar vertebrae are overly submerged, and a feeling of bottoming is likely to occur, which is not preferable. The smaller the static spring constant, the better. In particular, the slope of the pressure side curve at the time of deflection of 75% is an index for evaluating the feeling of bottoming, and the smaller this is, the better. It is better that the resonance vibration frequency and vibration transmissibility obtained in the vibration test are smaller. That is, 80% of the vibration riding comfort is vibration transmitted through the seat, and improvement of the transmission characteristics of these seats is considered to be an important factor for improving riding comfort.

【0004】以上の見地から、総合的に乗り心地の良い
シートクッションを設計するには、シートとして必要な
密度や硬度を保持したまま上記の各要因をバランス良く
組み合わすことが必要であるといえる。
From the above viewpoint, it can be said that in order to design a seat cushion that is totally comfortable to ride, it is necessary to combine the above factors in a well-balanced manner while maintaining the density and hardness required for the seat. ..

【0005】所で、従来のシートクッション用ポリウレ
タンフォームはホットモールドフォーム(以下、HOT
フォームと略す。)とコールドモールドフォーム(以
下、HRフォームと略す。)に大別される。一般にたわ
み量及びヒステレシスロスについてはHOTフォームの
方がHRフォームより大きく、沈み具合、はずみ具合の
点では優れているが、底付き感があり、また他の指標で
ある共振振動周波数についてはHRフォームより大き
く、伝達特性の点で劣っている。一方、HRフォームは
一般に共振振動周波数においてHOTフォームに勝って
いるが、共振点における振動伝達率が高く、かつ硬くて
はずみ易いという性質を有している。
By the way, the conventional polyurethane foam for seat cushion is a hot mold foam (hereinafter, referred to as HOT).
Abbreviated as form. ) And cold mold foam (hereinafter abbreviated as HR foam). Regarding the amount of deflection and hysteresis loss, HOT foam is generally larger than HR foam and is superior in terms of sinking and bouncing, but there is a feeling of bottoming and HR foam is another index for resonance vibration frequency. It is larger and inferior in transfer characteristics. On the other hand, the HR foam is generally superior to the HOT foam at the resonance vibration frequency, but has a high vibration transmissibility at the resonance point, and is hard and easy to bounce.

【0006】以上のごとく、従来型のフォームはいずれ
も、クッション特性の指標といわれる前記の各要因をバ
ランスよく充足したものではなく、したがってそれ単独
でも総合的に乗り心地の良いシートクッション用ポリウ
レタンフォームの開発が望まれていた。
As described above, none of the conventional foams satisfies the above-mentioned factors, which are said to be indicators of cushioning characteristics, in a well-balanced manner, and therefore, by itself, it is a polyurethane foam for a seat cushion that is totally comfortable to ride. Was desired to be developed.

【0007】[0007]

【発明が解決しようとする課題】本発明はそれ単独でも
シートクッション用ポリウレタンフォームとして好適な
クッション性、即ち沈み具合、柔らかさ、はずみ具合を
有すると共に、優れた動的振動特性を供えたポリウレタ
ンフォームの製造方法を提供することを目的とする。
The present invention, by itself, has a cushioning property suitable as a polyurethane foam for a seat cushion, that is, a degree of sinking, a softness, and a degree of bounce, and a polyurethane foam having excellent dynamic vibration characteristics. It aims at providing the manufacturing method of.

【0008】[0008]

【課題を解決するための手段】上記の目的を達成すべ
く、本研究者らは鋭意研究を重ねた結果、ポリウレタン
フォーム形成用組成物として、そのポリオール成分中
に、特定な第2級芳香族アミンを少量添加・配合したも
のを使用することにより、上記の目的を達成し得ること
を見出だし、本発明を完成するに至った。
[Means for Solving the Problems] As a result of intensive research conducted by the present inventors, in order to achieve the above object, as a composition for forming polyurethane foam, a specific secondary aromatic compound is contained in its polyol component. It has been found that the above object can be achieved by using a product to which a small amount of amine has been added and blended, and the present invention has been completed.

【0009】即ち、本発明はポリオール、触媒、発泡
剤、その他の添加剤からなるポリオール成分とポリイソ
シアネート成分とを反応させてポリウレタンフォームを
製造する方法において、下記の一般式 で示される第2級芳香族アミンを、上記ポリオール成分
中のポリエーテルポリオール100重量部当り0.5〜
5重量部配合したものを用いることを特徴とする乗り心
地の改良されたシートクッション用ポリウレタンフォー
ムの製造方法に関わる。なお、この方法はホットモール
ドプロセスによりこの種のシートクッション用ポリウレ
タンフォームを製造する上に特に好適に使用しうる。
That is, the present invention relates to a method for producing a polyurethane foam by reacting a polyol component composed of a polyol, a catalyst, a foaming agent, and other additives with a polyisocyanate component. 0.5 to 100 parts by weight of the polyether polyol in the above polyol component.
The present invention relates to a method for producing a polyurethane foam for a seat cushion having an improved riding comfort, which is characterized by using 5 parts by weight. It should be noted that this method can be particularly suitably used for producing a polyurethane foam for a seat cushion of this kind by a hot molding process.

【0010】本発明において使用するポリオールとして
は、汎用のポリエーテルポリオール、ポリマーポリオー
ル等すべて使用可能であるが好ましくは水酸基価20〜
65の範囲の2〜3価のポリオキシプロピレンポリオー
ル或いはポリオキシエチレンプロピレンポリオールをそ
れぞれ単独に、或いはそれらを組合せて使用される。ポ
リイソシアネート成分としては、公知の少なくとも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、
例えばTDI、TODI、NDI、XDI、PAPI、
ポリメリックイソシアネート等を単独又は併用して使用
することができる。また、ポリオールを加えてプレポリ
マー化ないしはセミプレポリマー化したものも使用でき
る。
As the polyol used in the present invention, all general-purpose polyether polyols, polymer polyols and the like can be used, but the hydroxyl value is preferably from 20 to 20.
The polyoxypropylene polyol or the polyoxyethylene propylene polyol having a valency of 65 in the range of 65 may be used alone or in combination. As the polyisocyanate component, all known at least bifunctional polyisocyanates can be used,
For example, TDI, TODI, NDI, XDI, PAPI,
Polymeric isocyanate or the like can be used alone or in combination. Further, a prepolymer or a semiprepolymer obtained by adding a polyol can also be used.

【0011】本発明において、ポリオール成分とポリイ
ソシアネート成分を反応させてポリウレタンフォームを
製造する場合、イソシアネートインデックスは、所望の
フォーム特性に基づいて、90〜110の範囲に調整す
るのが望ましい。
In the present invention, when a polyurethane foam is produced by reacting a polyol component and a polyisocyanate component, the isocyanate index is preferably adjusted within the range of 90 to 110 based on desired foam characteristics.

【0012】更に、触媒及び発泡剤としては、モールド
フォーム用として公知のものがすべて使用可能である
が、特に後者については地球環境保護の観点から、水ま
たは水に少量の代替フロンを添加した発泡剤系が好適で
ある。
Further, as the catalyst and the foaming agent, all the known ones for mold foams can be used. Especially, the latter is foamed by adding water or a small amount of CFC substitute to water from the viewpoint of global environment protection. Agent systems are preferred.

【0013】その他必要に応じ、公知のモールドフォー
ム用整泡剤、難燃剤、充填剤、顔料等が使用される。
Other known foam stabilizers for mold foams, flame retardants, fillers, pigments and the like may be used as required.

【0014】本発明においては、特に前記一般式で示さ
れる第2級芳香族アミン類をポリオール100重量部当
り0.5〜5重量部、好ましくは0.5〜2.5重量部
添加して用いる。この第2級芳香族アミン類は後述する
如くフォームのクッション特性の改良に顕著な効果を発
揮する。
In the present invention, the secondary aromatic amine represented by the above general formula is added in an amount of 0.5 to 5 parts by weight, preferably 0.5 to 2.5 parts by weight, per 100 parts by weight of the polyol. To use. These secondary aromatic amines exert a remarkable effect in improving the cushioning characteristics of the foam as described later.

【0015】該第2級芳香族アミン類の具体例として
は、4,4′−ビス−(メチルアミノ)−ジフェニルメ
タン、4,4′−ビス−(エチルアミノ)−ジフェニル
メタン、4−メチルアミノ−4′−エチルアミノ−ジフ
ェニルメタン、4−メチルアミノ−4′−n−プロピル
アミノ−ジフェニルメタン等を挙げることができる。
Specific examples of the secondary aromatic amines include 4,4'-bis- (methylamino) -diphenylmethane, 4,4'-bis- (ethylamino) -diphenylmethane and 4-methylamino-. 4'-ethylamino-diphenylmethane, 4-methylamino-4'-n-propylamino-diphenylmethane and the like can be mentioned.

【0016】R、R′の炭素数が4以上になるとアルキ
ル基の立体障害により反応速度が遅くなって好ましくな
い。これらの架橋剤は単独で、或いは併用して用いる事
ができる。その添加量が0.5重量部より少ないと添加
効果が著しく減少し、5重量部以上ではフォーム特性の
バランスが崩れ、例えばシートクッションとして要求さ
れる他の特性レベルを維持したまま振動特性を改良する
という初期の目的が達成されない。
When the carbon number of R and R'is 4 or more, the reaction rate becomes slow due to steric hindrance of the alkyl group, which is not preferable. These cross-linking agents can be used alone or in combination. If the addition amount is less than 0.5 parts by weight, the effect of addition is significantly reduced, and if it is 5 parts by weight or more, the balance of foam characteristics is lost, and for example, vibration characteristics are improved while maintaining other characteristic levels required for a seat cushion. The initial goal of doing is not achieved.

【0017】[0017]

【作用】この発明は原料ポリオール成分中に特定な第2
級芳香族アミンを添加使用したので、従来のHOTフォ
ームやHRフォームでは達成し得なかったクッション性
と動的振動特性の両特性を共にバランス良く兼備させる
ことができ、このポリウレタンフォームを単独で使用し
た場合にも、より乗り心地の改良されたシートクッショ
ンが得られる。また、従来のモールドプロセス、特にホ
ットモールドプロセスがそのまま適用できるので経済的
にも有利である。
The present invention has the second characteristic of the raw material polyol component.
Since a high-grade aromatic amine is added and used, both cushioning properties and dynamic vibration characteristics, which could not be achieved with conventional HOT foams and HR foams, can be provided in a well-balanced manner, and this polyurethane foam is used alone. Also in the case of doing, a seat cushion with improved riding comfort can be obtained. Further, the conventional molding process, especially the hot molding process can be applied as it is, which is economically advantageous.

【0018】[0018]

【実施例】以下、実施例に基づき本発明を具体的に説明
する。表1に示す原料成分(単位;重量部)を用いて自
動者用シートクッションパッド及び特性評価用テストピ
ースを作製した。特に前者についてはホットモールドプ
ロセスにのっとり、ポリオール成分Aとポリイソシアネ
ート成分Bをミキシングヘッドに供給し、吐出ノズルよ
り約35℃に設定された発泡金型の下型に注入し、上型
を閉じ、約100℃×10分間加熱オーブン中を通過さ
せ、しかる後金型温度を約45℃に冷却して脱型し、自
動車用シートクッションパッドを得た。次に、このシー
トクッション用ポリウレンフォームの特性を評価するた
め、400x400x100t定尺金型を使用してテス
トピースを成形し、このテストピースについて、JAS
O B−407及び408に準じ各特性を測定した。結
果を比較例(HOTフォーム)とともに表1及び図1〜
3に示す。なお、図1〜3には代表的HRフォームに関
する測定結果を参考までに付記した。
EXAMPLES The present invention will be specifically described below based on examples. Using the raw material components (unit: parts by weight) shown in Table 1, a seat cushion pad for an operator and a test piece for characteristic evaluation were produced. Particularly in the former case, the polyol component A and the polyisocyanate component B are supplied to the mixing head according to the hot molding process, injected from the discharge nozzle into the lower mold of the foaming mold set at about 35 ° C., and the upper mold is closed. After passing through a heating oven at about 100 ° C. for 10 minutes, the mold temperature was then cooled to about 45 ° C. and the mold was removed to obtain an automobile seat cushion pad. Next, in order to evaluate the properties of this polyuren foam for seat cushion, a test piece was molded using a 400x400x100t fixed-length mold, and this test piece was manufactured by JAS.
Each property was measured according to OB-407 and 408. The results are shown in Table 1 and FIG. 1 together with the comparative example (HOT foam).
3 shows. In addition, the measurement result regarding a typical HR foam is additionally shown in FIGS.

【0019】表1から明らかなごとく、本発明の方法に
より得られるポリウレタンフォームは、比較例として示
したHOTフォームと比べヒステレシスロスが大きく
(はずみ難い)、エネルギー吸収性の高いフォームであ
ることが認められる。この事は自由振動曲線(図2)か
らも明らかであり、この曲線図より求めた本発明のフォ
ームの自由反発率は3.1%であって、従来のフォーム
の自由反発率(HOTフォーム14.5%、HRフォー
ム59.6%)に比して極めて低い反発性能を示す。
As is clear from Table 1, the polyurethane foam obtained by the method of the present invention has a larger hysteresis loss than the HOT foam shown as a comparative example (it is hard to bounce) and has high energy absorption. Be done. This is also clear from the free vibration curve (FIG. 2), and the free restitution rate of the foam of the present invention obtained from this curve diagram is 3.1%, which is the free restitution rate of the conventional foam (HOT foam 14). 0.5%, HR foam 59.6%), which shows extremely low resilience performance.

【0020】図1は各フォームの荷重−たわみ曲線図で
あり、図において1は本発明のフォーム、2は従来型H
OTフォーム、3はHRフォームに関するものである。
この図において、フォーム1とフォーム2の75%たわ
み時における加圧側曲線の傾き(θ1 とθ2 )はθ1
θ2 とフォーム1の方が小さく本発明では従来型ホット
モールドフォームより底付き感の改良されたものが得ら
れる。なお、表1のヒステレシスロスは当該図1より常
法により求めた値である。
FIG. 1 is a load-deflection curve diagram of each foam, in which 1 is the foam of the present invention and 2 is a conventional type H
OT foam and 3 relate to HR foam.
In this figure, the slopes (θ 1 and θ 2 ) of the pressurizing side curve when Form 1 and Form 2 are deflected by 75% are θ 1 <
The size of θ 2 and foam 1 are smaller, and in the present invention, the one having an improved feeling of bottoming is obtained as compared with the conventional hot mold foam. The hysteresis loss in Table 1 is a value obtained by the usual method from FIG.

【0021】更に本発明のフォームは、図3に示すよう
に、周波数3〜5Hzの領域において振動伝達率が従来
フォームより低く押さえられ、しかも共振によるピーク
が現れないという特徴を有し、振動乗り心地特性の著し
く改良されたフォームといえる。
Further, as shown in FIG. 3, the foam of the present invention is characterized in that the vibration transmissibility is suppressed to be lower than that of the conventional foam in the frequency range of 3 to 5 Hz, and the peak due to resonance does not appear. It can be said that the foam has remarkably improved comfort characteristics.

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【発明の効果】以上の通り本発明は、従来のHOTフォ
ーム(ホットモールドフォーム)と比較して、これとほ
ぼ同等の密度、たわみ量を有するにも拘らず、底付き感
が少なく、低反発性を示し、しかも振動乗り心地特性の
著しく改善されたシートクッション用ポリウレタンフォ
ームを、従来のモールドプロセス、特にホットモールド
プロセスにより容易に製造する方法を提供する。
INDUSTRIAL APPLICABILITY As described above, according to the present invention, compared with the conventional HOT foam (hot mold foam), although it has almost the same density and deflection amount, it has less feeling of bottoming and low resilience. The present invention provides a method for easily manufacturing a polyurethane foam for a seat cushion, which exhibits excellent properties and has significantly improved vibration riding comfort characteristics, by a conventional molding process, particularly a hot molding process.

【図面の簡単な説明】[Brief description of drawings]

【図1】実施例に示した本発明のフォーム及び従来型H
OTフォームとHRフォームの荷重−たわみ曲線図。
FIG. 1 Foams of the invention and conventional H shown in the examples.
The load-deflection curve figure of OT foam and HR foam.

【図2】上記各フォームの自由振動曲線(自由反発率)
図。
[Fig. 2] Free vibration curve (free repulsion rate) of each form above
Fig.

【図3】同じく上記各フォームの振動特性図である。FIG. 3 is a vibration characteristic diagram of each foam.

【符号の説明】[Explanation of symbols]

θ1 、θ2 ……荷重−たわみ曲線の75%たわみ時にお
ける加圧側曲線を引いた接線の傾き
θ 1 , θ 2 ...... Inclination of the tangent line drawn by the pressure side curve when the load-deflection curve is deflected by 75%

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08G 101:00) C08L 75:04 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area C08G 101: 00) C08L 75:04

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ポリオール、触媒、発泡剤、その他の添
加剤からなるポリオール成分とポリイソシアネート成分
とを反応させてポリウレタンフォームを製造する方法に
おいて、下記の一般式 で示される第2級芳香族アミンを、上記ポリオール成分
中のポリオール100重量部当り0.5〜5重量部配合
したものを用いることを特徴とする乗り心地の改良され
たシートクッション用ポリウレタンフォームの製造方
法。
1. A method for producing a polyurethane foam by reacting a polyol component comprising a polyol, a catalyst, a foaming agent, and other additives with a polyisocyanate component, wherein A polyurethane foam for a seat cushion with improved riding comfort, characterized in that 0.5 to 5 parts by weight of a secondary aromatic amine represented by the above is blended per 100 parts by weight of the polyol in the polyol component. Production method.
JP13355192A 1992-05-26 1992-05-26 Method for producing polyurethane foam for seat cushion with improved ride comfort Expired - Fee Related JP3279640B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13355192A JP3279640B2 (en) 1992-05-26 1992-05-26 Method for producing polyurethane foam for seat cushion with improved ride comfort

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13355192A JP3279640B2 (en) 1992-05-26 1992-05-26 Method for producing polyurethane foam for seat cushion with improved ride comfort

Publications (2)

Publication Number Publication Date
JPH05320304A true JPH05320304A (en) 1993-12-03
JP3279640B2 JP3279640B2 (en) 2002-04-30

Family

ID=15107463

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13355192A Expired - Fee Related JP3279640B2 (en) 1992-05-26 1992-05-26 Method for producing polyurethane foam for seat cushion with improved ride comfort

Country Status (1)

Country Link
JP (1) JP3279640B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6759448B2 (en) 2001-08-06 2004-07-06 Asahi Glass Company, Limited Flexible polyurethane foam, its production method and material system for its production
US6890966B2 (en) 2001-05-11 2005-05-10 Suzuki Motor Corporation Process for the production of a lightweight cold urethane
US7388036B2 (en) 2003-11-26 2008-06-17 Asahi Glass Company, Limited Flexible polyurethane foam, process for its production, and seat for automobile employing it
US7635724B2 (en) 2005-05-25 2009-12-22 Asahi Glass Company, Limited Flexible polyurethane foam, process for its production, and seat for automobile using the flexible polyurethane foam
US7825166B2 (en) 2005-05-25 2010-11-02 Asahi Glass Company, Limited Flexible polyurethane foam, process for its production, and seat for automobile using the flexible polyurethane foam

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6890966B2 (en) 2001-05-11 2005-05-10 Suzuki Motor Corporation Process for the production of a lightweight cold urethane
US6759448B2 (en) 2001-08-06 2004-07-06 Asahi Glass Company, Limited Flexible polyurethane foam, its production method and material system for its production
US7388036B2 (en) 2003-11-26 2008-06-17 Asahi Glass Company, Limited Flexible polyurethane foam, process for its production, and seat for automobile employing it
US7635724B2 (en) 2005-05-25 2009-12-22 Asahi Glass Company, Limited Flexible polyurethane foam, process for its production, and seat for automobile using the flexible polyurethane foam
US7825166B2 (en) 2005-05-25 2010-11-02 Asahi Glass Company, Limited Flexible polyurethane foam, process for its production, and seat for automobile using the flexible polyurethane foam

Also Published As

Publication number Publication date
JP3279640B2 (en) 2002-04-30

Similar Documents

Publication Publication Date Title
US5093380A (en) Polyurethane flexible foam and method for its production
US6521674B1 (en) Latex-like flexible polyurethane foam and process for making same
KR100541314B1 (en) Low Resilience, Low Frequency Molded Polyurethane Foam
CA2055292A1 (en) Isocyanate-terminated prepolymer and flexible polyurethane foam prepared therefrom
CA2396679A1 (en) Flexible polyurethane foam, its production method and material system for its production
JPH03199223A (en) Polyurethane foam for cushioning material
JP3992869B2 (en) Energy-absorbing flexible polyurethane foam and method for producing the same
JP2014167115A (en) Polyurethane foam formulation, product and method
JP3880699B2 (en) Method for producing flexible polyurethane foam
JP3279640B2 (en) Method for producing polyurethane foam for seat cushion with improved ride comfort
JPH0912667A (en) Molded flexible polyurethane foam
JPH0131536B2 (en)
JPH05271379A (en) Preparation of open-cell elastic flexible polyurethane foam
JP2816806B2 (en) Back cushion for vehicle seat and method of manufacturing the same
JPH08231677A (en) Preparation of high elasticity polyurethane foam
JPH0368620A (en) Production of highly resilient polyurethane foam
JP3214781B2 (en) Method for producing flexible polyurethane foam
WO2024080268A1 (en) Seat pad
AU631751B2 (en) Energy-absorbing flexible polyurethane foam
JPH08208800A (en) Highly elastic flexible polyurethane foam
JP3224957B2 (en) High elasticity flexible polyurethane foam and method for producing the same
WO2024080267A1 (en) Seat pad
JP2004043811A (en) Flexible polyurethane molded foam
JP3502149B2 (en) Hygroscopic polyurethane foam and method for producing the same
JP2006008773A (en) Flexible polyurethane foam and its manufacturing method

Legal Events

Date Code Title Description
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20020108

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080222

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090222

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090222

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100222

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100222

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110222

Year of fee payment: 9

LAPS Cancellation because of no payment of annual fees