JPS60195118A - Urethane handle - Google Patents

Urethane handle

Info

Publication number
JPS60195118A
JPS60195118A JP59050631A JP5063184A JPS60195118A JP S60195118 A JPS60195118 A JP S60195118A JP 59050631 A JP59050631 A JP 59050631A JP 5063184 A JP5063184 A JP 5063184A JP S60195118 A JPS60195118 A JP S60195118A
Authority
JP
Japan
Prior art keywords
urethane
handle
mdi
pigment
catalyst
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
JP59050631A
Other languages
Japanese (ja)
Inventor
Akira Mabuchi
馬渕 彰
Yoshio Ushida
牛田 芳雄
Yoshio Yamazaki
山崎 喜夫
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.)
Toyoda Gosei Co Ltd
Original Assignee
Toyoda Gosei 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 Toyoda Gosei Co Ltd filed Critical Toyoda Gosei Co Ltd
Priority to JP59050631A priority Critical patent/JPS60195118A/en
Publication of JPS60195118A publication Critical patent/JPS60195118A/en
Pending legal-status Critical Current

Links

Landscapes

  • Steering Controls (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To obtain an urethane handle with small temperature dependency, by molding using a semi-rigid integral skin polyurethane foam prepared from polyether polyol, polymer polyol, crosslinking agent, foaming agent, catalyst, pigment, etc. CONSTITUTION:The objective urethane handle can be obtained by carrying out a RIM molding circumferentially on core 1, using the following components: (A) polyether polyol and/or polymer polyol, (B) crosslinking agent (e.g. diethylene glycol), (C) foaming agent, (D) catalyst (e.g. triethylenediamine), (E) pigment, and (F) as isocyanate component, a mixture of pure MDI and crude MDI (pref. a weight ratio of the former to the latter falling between 9/1 and 4/6) to form semi-rigid integral urethane layer 2. Said pure MDI represents 4,4'-diphenylmethane diisocyanate, etc. whereas said crude MDI polymeric diphenylmethane diisocyanate, etc.

Description

【発明の詳細な説明】 この発明は湿度1Δ存性が小さいウレタンハンドルに閉
覆るものでdうる。
DETAILED DESCRIPTION OF THE INVENTION The present invention can be used to cover a urethane handle with a low humidity 1Δ sensitivity.

従来技術 従来のウレタンハンドルは例えばポリ:[−チルポリオ
ールとピュアMDIプレポリマーとよりなる半硬質イン
テグラルスキンポリウレタンフォーム(高密度の表皮層
と低密度の内部発泡層が一体に形成されているウレタン
ハンドル)からなりRI tVI (Re)) C1:
 i o n l n j e c t i o nM
o1dino)成形により作られている。そして、一般
にウレタンハンドルの感触は低温時では硬くなり、高温
時では柔かくなるという問題があつ lこ 。
Prior art A conventional urethane handle is made of, for example, a semi-rigid integral skin polyurethane foam (a urethane foam in which a high-density skin layer and a low-density internal foam layer are integrally formed) made of poly:[-chill polyol and pure MDI prepolymer. RI tVI (Re)) C1:
i o n l n j e c t i o n M
o1dino) is made by molding. Another problem is that urethane handles generally feel hard at low temperatures and soft at high temperatures.

発明の目的 この発明1、艮前記従来のウレタンハンドルの温度依存
性を改善するためになされたものであって、その目的は
従来のポリニーデルポリオールとMDIプレポリマーと
よりなる半硬質インテグラルスキンポリウレタンフA−
ムにて作られたウレタンハンドルJ、りも温度依存性に
優れ、低湿時には硬くならず、又、高温時には柔かくな
らないウレタンハンドルを提供することにある。
Purpose of the Invention This invention 1 was made in order to improve the temperature dependence of the conventional urethane handle, and its purpose is to improve the temperature dependence of the conventional urethane handle, and its purpose is to improve the temperature dependence of the conventional urethane handle, and its purpose is to improve the temperature dependence of the conventional urethane handle. Polyurethane foam A-
To provide a urethane handle J made of rubber, which has excellent temperature dependence, does not become hard at low humidity, and does not become soft at high temperature.

発明の構成 この発明のウレタンハンドルはポリエーテルポリオール
及び/又はポリマーポリオールと、栗橋剤2発泡剤、触
媒、顔料、及びイソシアナート成分としてピュアMDI
とクルードMDIの混合物とを用いた半硬質インテグラ
ルスキンポリウレタンフA−ムにて形成したものである
Structure of the Invention The urethane handle of the present invention comprises a polyether polyol and/or a polymer polyol, a chestnut crosslinking agent, two blowing agents, a catalyst, a pigment, and pure MDI as an isocyanate component.
It is formed from a semi-rigid integral skin polyurethane foam A using a mixture of MDI and crude MDI.

実施例 以下、この発明を11体化した=実施例を第1図及び第
2図に従って説明づる。
EXAMPLES Below, eleven examples of the present invention will be explained with reference to FIGS. 1 and 2.

この実施例のウレタンハンドル八はポリエーテルポリオ
ールどしC→ノシエックス15Δ−703(三官能基 
分子lit !−r OOO[三洋化成]二業株式会社
製」)を50Φ■部及びエフセノールG−510(=官
能基 分子fn5000r旭硝子株式会社製」)を5)
0小迅部、架橋剤としてジエチレングリコールを18重
量部、発泡剤としてフレオン−11を15車量部、触媒
どして1−リエチレンジアミンを0.7中小部、顔料(
ブラック)を6小迅部、ピコアMI) l /クルード
MDIとしてコロネーt”1051(N00%−29%
 ビコアM D1/クルードtvl l) l = 5
0 / 50 F日本ポリウレタン]二業株式会社製」
)を63重量部、さらにベンゾ1リアゾール系紫外線吸
収剤を0.5重恒部使用し、芯材1に対してRIM成形
を行うことにJ:す、同芯4第1の外周に半硬質インテ
グシル′クレタン層2を形成しでいる。
The urethane handle 8 in this example is polyether polyol C → Noshiex 15Δ-703 (trifunctional group
Molecule lit! -r OOO [Sanyo Kasei] Nigyo Co., Ltd.'') 50 Φ■ part and Efsenol G-510 (=functional group molecule fn5000r Asahi Glass Co., Ltd.'') 5)
18 parts by weight of diethylene glycol as a crosslinking agent, 15 parts by weight of Freon-11 as a blowing agent, 0.7 parts by weight of 1-lyethylenediamine as a catalyst, pigment (
Black) to 6 Kojinbe, Picoa MI) l / Crude MDI as Coronat t”1051 (N00%-29%
Bicore M D1/Clued tvl l) l = 5
0/50 F Japan Polyurethane] Manufactured by Nigyo Co., Ltd.
) and 0.5 parts by weight of a benzo-1-lyazole ultraviolet absorber, RIM molding was performed on the core material 1. Integusil'cretan layer 2 has been formed.

そしで、このウレタンハンドル八と従来のポリエーテル
ポリオールとピュアMDIプレポリマーとからなるウレ
タンハンドルBどの’(Q +、&依存性の比較試験を
行った。
Then, a comparative test was conducted on the dependence of this urethane handle 8 and urethane handle B made of a conventional polyether polyol and pure MDI prepolymer.

なお、比較試験に用いた従来のウレタンハンドルBはポ
リエーテルポリオールとしてザンエックスFA−703
(=官能基 分子15000[三洋化成工業株式会社製
」)を50重ω部及び1ノ−ンエックスFA−909(
三官能基 分子量6ooo r三洋化成工業株式会社製
」)を50重量部、架橋剤どじでエチレングリコールを
9小迅部、発泡剤どじてルAンー11を15車吊部、触
媒としてトリエチレンジアミンを1重量部、顔料(ブラ
ック)を6重量部、ピュアMDIとしてコロネー1〜1
0/l0(N00%−23% F日木ポリウレタンT業
株式会社製」)を65重足部、さらにベンゾ1〜リアゾ
ール系紫外線吸収剤を0.5中m部使用し、芯材1に対
してRIM成形を行うことにより、Ii’i]芯拐1の
芯層1半硬質インデグラルウレタン11”・12を形成
し−Cいる。
In addition, the conventional urethane handle B used in the comparative test was ZANX FA-703 as a polyether polyol.
(=functional group molecule 15000 [manufactured by Sanyo Chemical Industries, Ltd.]) with 50 weight ω parts and 1 non-X FA-909 (
50 parts by weight of trifunctional group, molecular weight 6 ooo r (manufactured by Sanyo Chemical Industries, Ltd.), 9 parts by weight of ethylene glycol as a crosslinking agent, 15 parts of Le A-11 as a blowing agent, and triethylenediamine as a catalyst. 1 part by weight, 6 parts by weight of pigment (black), Coronet 1-1 as pure MDI
0/l0 (N00%-23% F Hiki Polyurethane T Gyo Co., Ltd.) was used for 65 parts, and 0.5 parts of benzo-1 to lyazole-based ultraviolet absorbers were used for each core material. By performing RIM molding, semi-hard integral urethane 11'' and 12 of the core layer 1 of the core layer 1 are formed.

この試験はウレタンハンドル△、13を雰囲気温1、印
0°C,20’ C,=lO°C,60°C及び80°
Cの各温1長1ドに載置し、ぞのどさのウレタンハンド
ルΔ、13の(l!l!度を8111定づることに1、
り行われた。なdj、硬度測定に使用した硬Ig、:l
はアスカ−CI# Iu計(1高分−If Za式会?
I !!I!7) −c−h リ、この硬度t1ににっ
て泪測される硬度を以下タイプCの硬度という。
This test was carried out with the urethane handle △, 13 at an ambient temperature of 1, marked 0°C, 20'C, = lO°C, 60°C and 80°
Place the urethane handle Δ, 13 (l!
was held. dj, hardness Ig used for hardness measurement, :l
Is Asuka-CI# Iu total (1 high minute-If Za ceremony?
I! ! I! 7) -ch The hardness measured by this hardness t1 is hereinafter referred to as type C hardness.

この試験結束を横1i+11に雰囲気渇瓜をどり、縦軸
にI!I!度をどっC第2図に示す。
This test bundle is plotted horizontally as 1i+11, and the vertical axis is I! I! The degree is shown in Figure 2.

この第2図の)1.1冒旦依存性の特性グラフにJ、す
、この実施例のウレタンハンドルΔ(J従来のウレタン
パン1−ルBど比11−☆し−(’ (l(2M時には
(ゆくならず、高ン品口、1には柔かくなくなるという
ことが確81て・・き/こ 。
The characteristic graph of 1.1 temperature dependence in Fig. 2 shows the urethane handle of this example At 2M, it is certain that it will not be soft at 1 (it is 81 degrees).

なお、−一般にウレタンハンドルはこの硬度指数にJ3
いては通’7+’r iI!t!I衰70±5が感触に
最も適しており、又、硬度60以下の場合は柔かすぎて
芯材1の存在が判別できるようになるのでウレタンパン
1−ルどして不適当である。
Furthermore, in general, urethane handles have a hardness index of J3.
Teha Tsu'7+'r iI! T! An I decay of 70±5 is most suitable for the feel, and if the hardness is less than 60, it is too soft and the presence of the core material 1 can be discerned, making it unsuitable for use as a urethane pan.

次にピコアM l) I /クルードMDIの比率を5
0 / !j Oとして前記実施例と同様に成形し!こ
この発明のウレタンハンドルA1と、従来のピュアMD
IからイfるウレタンハンドルBと、クルードMD I
からなるウレタンハンドルCどの耐光性試験を行った。
Next, the ratio of picoa M l) I/crude MDI is 5
0/! j O and molded in the same manner as in the previous example! The urethane handle A1 of this invention and the conventional Pure MD
Urethane handle B from I and Crude MD I
A light resistance test was conducted on a urethane handle C made of:

なdj、前記クルードMDIからなるウレタンハンドル
Cはポリエーテル(四官能基 分子fJfv 7000
)を100小迅部、架橋剤どしてエチレングリコールを
5小迅部、発泡剤としてフレオン−11を1!5申11
部、触媒として1〜り土チレンシノ7ミンをO,!”)
重R部、顔料を6小迅部、クルー1〜′MDIを35重
量部、さらにベンゾ1〜リアゾ−ル系紫外線吸収剤を0
.5重量部使用し、芯材1に対して1<1M成形を行う
ことにより、間怠441の外周に半硬質インテグラルウ
レタン層2を形成したものである。
dj, the urethane handle C made of the crude MDI is polyether (tetrafunctional group molecule fJfv 7000
) to 100 parts, 5 parts to ethylene glycol as a crosslinking agent, 11 to 11 parts to Freon-11 as a blowing agent.
Part, O,! ”)
Heavy R part, 6 small parts of pigment, 35 parts by weight of Crew 1~'MDI, and 0 part of benzo~lyazole ultraviolet absorber.
.. By using 5 parts by weight and performing 1<1M molding on the core material 1, a semi-rigid integral urethane layer 2 was formed around the outer periphery of the gap 441.

この耐光性試験は一ノ1−ドメータ(83°Cの′fJ
A度条件下)で50時間経過後毎にウレタンハンドルに
対しC’I 0回ねじりを加えて生ずる亀裂発生時間を
測定したものである。
This light fastness test was carried out using a 1-dometer ('fJ at 83°C).
The urethane handle was twisted C'I 0 times every 50 hours under A degree conditions), and the crack generation time was measured.

1)11記試験の結束を以下の表に示り゛。1) The table below shows the results of the 11th test.

上記の表からウレタンハンドルΔ1はイの亀裂発生n−
′1間が1000時間以上あり、従来構成のつ1ノタン
ハンドル;3と遜色がない耐光性を確認覆ることができ
る。。
From the table above, the urethane handle Δ1 is the crack occurrence n-
'1 for more than 1,000 hours, and it can be confirmed that the light resistance is comparable to that of the conventional construction of the handle. .

なJ3、ピコツノM L) I /クルードMDIの比
率が9/1J、りも人さくなる場合、ピュアMDIの従
来のウレタンハンドルの9、r性ずなわち温度依存性が
大きくなるため好ましくない。又、ピュアMDl/クル
ードMDIの比率が/l/6よりも小さくなる場合には
クルードMDIの特性′りなわら引張強瓜、耐++h耗
V1、弾力性等のウレタンパン1−ルに要求される物性
が悲くなるため好ましくない。
If the ratio of I/crude MDI becomes 9/1J, it is not preferable because the 9/r properties of the conventional urethane handle of pure MDI, that is, the temperature dependence becomes large. In addition, when the ratio of pure MDl/crude MDI is smaller than /l/6, the properties of crude MDI, such as tensile strength, wear resistance V1, elasticity, etc. This is not desirable because the physical properties become poor.

なお、前記実施例ではポリエーテルポリオールを使用し
たがポリT−チルポリΔ−ルに代え(ポリマーポリオー
ルを使用しても作用効果は同じである。
In addition, although polyether polyol was used in the above embodiment, the effect is the same even if a polymer polyol is used instead of poly T-chill polyΔ-ol.

なお、ビー17MDIは/1./l−−ジフェニルメタ
ンジイソシアナート及びそのカルボジイミド変性体等の
略称であり、クルードMDIはポリメリックシフ、1.
ニルメクンジイソシアナ−1への略杓−(ある。さらに
これらのプレポリマーもρ含する。
In addition, Bee 17MDI is /1. /l--It is an abbreviation for diphenylmethane diisocyanate and its carbodiimide modified product, etc. Crude MDI is Polymeric Schiff, 1.
Nirmekun diisocyanate-1 (approximately ladle-) (in addition, these prepolymers also contain ρ.

発明の効果 以上、詳述したようにこの発明はポリエーテルポリオー
ル及び/又はポリマーポリメールど、架橋剤、発泡剤、
触媒、顔料、及びイワシアナ−1〜成分としてピュアM
DIとクルードMDIの混合物とを用いた半硬質インテ
グラルスキンポリウレタンフA−ムにで形成したことに
より、従来のポリエーテルポリオールどMDIプレポリ
マーどよりなる半硬質インデグラルスキンポリウレタン
フォームにて作られたウレタンハンドルよりも温度依存
性に優れ、低温時には硬くならず、又、高温時には柔か
くならない効果を秦するので産業利用1優れた発明であ
る。
Effects of the Invention As described in detail, the present invention utilizes polyether polyols and/or polymer polymers, crosslinking agents, blowing agents,
Catalyst, Pigment, and Sardine Ana-1 ~ Pure M as Ingredients
By forming a semi-rigid integral skin polyurethane foam using a mixture of DI and crude MDI, it is possible to create a semi-rigid integral skin polyurethane foam made of a conventional polyether polyol or MDI prepolymer. This is an excellent invention for industrial use because it has better temperature dependence than other urethane handles, does not become hard at low temperatures, and does not become soft at high temperatures.

【図面の簡単な説明】 第1図(よウレタンハンドルの断面図、第2図はウレタ
ンハンドルの温度依存性を示すグラフである。 芯材1.半硬質ウレタン層2゜ q、l :’I 出 願 人 豊D」合成株式会社代 
理 人 弁理士 J4 [1j le宜第1図 第2図 0 20 40 60 80 雰囲気温度 (C)
[Brief Description of the Drawings] Figure 1 (cross-sectional view of the urethane handle), Figure 2 is a graph showing the temperature dependence of the urethane handle. Core material 1. Semi-rigid urethane layer 2゜q,l:' Applicant Yutaka D” Gosei Co., Ltd.
Attorney Patent attorney J4 [1j lei Figure 1 Figure 2 0 20 40 60 80 Ambient temperature (C)

Claims (1)

【特許請求の範囲】 1、ポリエーテルポリオール及び/又はポリマーポリオ
ールど、架橋剤、発泡剤、触媒、顔料、及びイソシアノ
゛−1〜成分としてピュアMDIとクルードM1)1の
11配合物とを用いた半fN?ffインデグラルスキン
ポリウレタンフA−ムにて形成したことを12J徴どり
るつ1ノタンハンドル。 2、ビIツノへ41つ1とクルードM1〕1の)14合
比率4、’L ;Q ii!比C9/′−1〜4/6で
あることを特徴とする特R’を請求の範囲第1項に記載
のウレタンハンドル。
[Claims] 1. Using pure MDI and Crude M1) 11 blends as components such as polyether polyol and/or polymer polyol, crosslinking agent, blowing agent, catalyst, pigment, and isocyanol. The half-fN you had? ff A 1-note tan handle featuring 12J made of integral skin polyurethane foam. 2, B I horn to 41 1 and Crude M1] 1) 14 ratio 4, 'L ;Q ii! The urethane handle according to claim 1, characterized in that the ratio R' is C9/'-1 to 4/6.
JP59050631A 1984-03-15 1984-03-15 Urethane handle Pending JPS60195118A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59050631A JPS60195118A (en) 1984-03-15 1984-03-15 Urethane handle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59050631A JPS60195118A (en) 1984-03-15 1984-03-15 Urethane handle

Publications (1)

Publication Number Publication Date
JPS60195118A true JPS60195118A (en) 1985-10-03

Family

ID=12864317

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59050631A Pending JPS60195118A (en) 1984-03-15 1984-03-15 Urethane handle

Country Status (1)

Country Link
JP (1) JPS60195118A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6490868A (en) * 1987-09-30 1989-04-07 Toyoda Gosei Kk Urethane coated steering wheel
JP2000211530A (en) * 1999-01-25 2000-08-02 Nippon Plast Co Ltd Steering wheel and manufacture thereof
JP2011153316A (en) * 2008-04-25 2011-08-11 Toyo Polymer Co Ltd Polyurethane foam and polishing pad
WO2018189972A1 (en) * 2017-04-11 2018-10-18 オートリブ ディベロップメント エービー Polyurethane foam production method, steering wheel production method, and steering wheel

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS509698A (en) * 1973-05-30 1975-01-31

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS509698A (en) * 1973-05-30 1975-01-31

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6490868A (en) * 1987-09-30 1989-04-07 Toyoda Gosei Kk Urethane coated steering wheel
JP2000211530A (en) * 1999-01-25 2000-08-02 Nippon Plast Co Ltd Steering wheel and manufacture thereof
JP2011153316A (en) * 2008-04-25 2011-08-11 Toyo Polymer Co Ltd Polyurethane foam and polishing pad
JPWO2009131106A1 (en) * 2008-04-25 2011-08-18 トーヨーポリマー株式会社 Polyurethane foam and polishing pad
JP4897082B2 (en) * 2008-04-25 2012-03-14 トーヨーポリマー株式会社 Polyurethane foam and polishing pad
WO2018189972A1 (en) * 2017-04-11 2018-10-18 オートリブ ディベロップメント エービー Polyurethane foam production method, steering wheel production method, and steering wheel
JPWO2018189972A1 (en) * 2017-04-11 2020-01-09 オートリブ ディベロップメント エービー Polyurethane foam manufacturing method, steering wheel manufacturing method and steering wheel

Similar Documents

Publication Publication Date Title
CN105399917B (en) Organic silicon modified thermoplastic polyurethane elastomer and preparation method thereof
CN108383963A (en) A kind of composition and preparation method thereof and the application in power mutagens color Material Field
EP3581603A1 (en) Thermoplastic organosilicone-polyurethane elastomer and preparation method therefor
JP2001507070A (en) Open cell rigid polyurethane foam
Sur et al. Preparation and Properties of DMF‐Based Polyurethanes for Wet‐Type Polyurethane Artificial Leather
CN107129601B (en) A kind of athletic protective vibration-absorptive material and preparation method thereof
JPS60195118A (en) Urethane handle
US3575896A (en) Microcellular foams having a low glass transition temperature
US6020392A (en) Polyurea elastomeric microcellular foam
JP2008222769A5 (en)
JPS63101167A (en) Steering wheel applied with skin
US7259222B2 (en) Compositions for use in golf balls
CA2887234C (en) Non-cytotoxic urethane elastomer
JPS61176624A (en) Light-or medium-duty tire
KR20160094350A (en) Foamable composition for polyurethane foam, polyurethane foam, and jounce bumper comprising the same
US4301270A (en) Curative for castable polyurethanes
JPH07292061A (en) Polyurethane
JP2004059706A (en) Process for producing thermoplastic polyurethane elastomer
JP2007182533A (en) Polyurethane foamed article and method for producing the same
JP2003076087A (en) Semiconducting member for electrophotographic device
JPH06184367A (en) Polymer alloy
JP2023079122A (en) steering wheel
JPS6213427A (en) Production of coarse-cellular flexible urethane foam
JP2023015984A (en) Filler for puncture-free tire and its manufacturing method
JP2019077379A (en) Steering wheel