WO2012132912A1

WO2012132912A1 - Polyol composition and polyurethane resin

Info

Publication number: WO2012132912A1
Application number: PCT/JP2012/056621
Authority: WO
Inventors: 隆也川村; 欣範山田
Original assignee: 第一工業製薬株式会社
Priority date: 2011-03-25
Filing date: 2012-03-15
Publication date: 2012-10-04
Also published as: JP5707197B2; JP2012201800A

Abstract

The present invention addresses the problem of providing a polyol composition and the like whereby it is possible to make a polyurethane resin which has superior relative impact resistance at low temperatures and for which deformation is suppressed at high temperatures. Provided are a polyol composition and the like, characterized in comprising: a polybutadiene polyol (a), the molecule of which has a polybutadiene structure and a plurality of hydroxyl groups; an amine polyol (b), which is a tertiary amine the molecule of which has a plurality of hydroxyl groups; and an alkylene diol (c), the molecule of which has two primary hydroxyl groups and which has a solidification point of at most -20°C.

Description

Polyol composition and polyurethane resin

The present invention relates to a polyol composition and a polyurethane resin. Specifically, for example, the present invention relates to a polyol composition used as a raw material of a polyurethane resin for protecting a steel material, and a polyurethane resin obtained by reacting the composition with a polyisocyanate compound.

Conventionally, various types of polyol compositions have been known. Specifically, for example, those containing polybutadiene polyol having a polybutadiene structure and a plurality of hydroxyl groups in the molecule and castor oil are known. (Patent Document 1).

Such a polyol composition is used, for example, in applications where it is mixed with a polyisocyanate compound immediately before use and applied to the surface of a steel material to form a protective material for a polyurethane resin on the surface of the steel material.

However, such a polyol composition has a problem that a polyurethane resin produced using the composition has a relatively high impact resistance at a low temperature, but can be relatively easily deformed by an external force at a high temperature. That is, there is a problem that a polyurethane resin produced using such a polyol composition is not necessarily excellent in deformation resistance at a high temperature required for the use of a protective material for the steel material surface.

JP-A 64-79268

The present invention has been made in view of the above-mentioned problems and the like, and an object thereof is to provide a polyol composition capable of producing a polyurethane resin which is relatively excellent in impact resistance at low temperatures and whose deformation is suppressed at high temperatures. Another object of the present invention is to provide a polyurethane resin which is relatively excellent in impact resistance at low temperatures and whose deformation is suppressed at high temperatures.

In order to solve the above problems, the polyol composition according to the present invention comprises a polybutadiene polyol (a) having a polybutadiene structure and a plurality of hydroxyl groups in the molecule, and an amine polyol (a tertiary amine having a plurality of hydroxyl groups in the molecule). and b) and an alkylene diol (c) having two primary hydroxyl groups in the molecule and having a freezing point of −20 ° C. or lower.

The polyol composition according to the present invention preferably further contains a castor oil-based polyol (d).

Moreover, it is preferable that the polyol composition according to the present invention further contains an amine compound (e) having an active hydrogen-containing amino group in the molecule.

The polyurethane resin according to the present invention is characterized in that the polyol composition is reacted with a polyisocyanate compound having a plurality of isocyanate groups in the molecule.

The polyol composition according to the present invention has the effect of being able to produce a polyurethane resin that is relatively excellent in impact resistance at low temperatures and relatively suppressed in deformation at high temperatures. Moreover, the polyurethane resin according to the present invention has an effect that it is relatively excellent in impact resistance at a low temperature and is relatively prevented from being deformed at a high temperature.

Hereinafter, a first embodiment of the polyol composition according to the present invention will be described.

The polyol composition of the present embodiment comprises a polybutadiene polyol (a) having a polybutadiene structure and a plurality of hydroxyl groups in the molecule, an amine polyol (b) which is a tertiary amine having a plurality of hydroxyl groups in the molecule, and a molecule. And alkylene diol (c) having two primary hydroxyl groups and having a freezing point of -20 ° C. or lower.

The polyol composition becomes a polyurethane resin by reacting with a polyisocyanate compound described later.

The polyol composition is further characterized in that the polyurethane resin produced by reacting the polyol composition with a polyisocyanate compound described later is more excellent in impact resistance at low temperatures and more excellent in deformation resistance at high temperatures. It is preferable to contain a castor oil-based polyol or (e) an amine compound having an active hydrogen-containing amino group in the molecule.
Further, the polyol composition preferably contains a powdery inorganic filler in that the polyurethane resin can be more excellent in impact resistance at low temperatures and more excellent in deformation resistance at high temperatures. .

The polybutadiene polyol (a) may have a polybutadiene structure in which 1,3-butadiene is trans 1,4-bonded, or has a polybutadiene structure in which 1,3-butadiene is cis 1,4-bonded. Alternatively, it may have a polybutadiene structure in which 1,3-butadiene is bonded to 1,2. Moreover, you may have a polybutadiene structure in which these bonds were mixed.
As said polybutadiene polyol, what has a polybutadiene structure and two hydroxyl groups in a molecule | numerator is preferable, and what has a hydroxyl group at the both ends of a chain | strand-shaped polybutadiene structure is more preferable, respectively.

The polybutadiene polyol has an average hydroxyl value determined according to JIS K1557-1 (Method A) of preferably 20 to 250 mgKOH / g, and more preferably 45 to 105 mgKOH / g.
When the average hydroxyl value of the polybutadiene polyol is 20 mgKOH / g or more, there is an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperatures. Moreover, there exists an advantage that the impact resistance in the low temperature of a polyurethane resin can become more excellent because it is 250 mgKOH / g or less.

Examples of the polybutadiene polyol include conventionally known general ones. For example, the trade name “Poly bd R-45 HT” (manufactured by Idemitsu Kosan Co., Ltd.) and the trade name “Poly bd R-15 HT” (Idemitsu Kosan Co., Ltd.). (Commercially available) can be used.

The polybutadiene polyol can be used singly or in combination of two or more.

The polybutadiene polyol is preferably contained in the polyol composition in an amount of 15 to 30 parts by weight, more preferably 20 to 25 parts by weight.
When the polybutadiene polyol is contained in the polyol composition in an amount of 15 parts by weight or more, there is an advantage that the polyurethane resin can have more excellent impact resistance at low temperatures. Moreover, when 30 weight part or less is contained, there exists an advantage that the deformation resistance in the high temperature of the said polyurethane resin can become more excellent.

Since the amine polyol (b) is a tertiary amine having a plurality of hydroxyl groups in the molecule, it has both the properties of the amine and the properties of the polyol.

Examples of the amine polyol include aromatic monoamines such as aniline, aromatic polyamines such as toluenediamine, diethyltoluenediamine, 4,4′-diamino-3,3′-diethyldiphenylmethane, ethylenediamine, hexamethylenediamine, and diethylenetriamine. And those obtained by adding an alkylene oxide having 2 to 4 carbon atoms to an amine such as an aliphatic polyamine.
Examples of the alkylene oxide having 2 to 4 carbon atoms include ethylene oxide, propylene oxide, butylene oxide and the like.

Specifically, the amine polyol is preferably one in which an alkylene oxide is added to the aromatic monoamine in that the polyurethane resin can be more excellent in strength, and an alkylene oxide is added to aniline. Is more preferable. Further, a product obtained by adding propylene oxide to aniline is more preferable.

The amine polyol preferably has an average hydroxyl value determined in accordance with JIS K1557-1 (Method A) of 350 to 500 mgKOH / g.
When the average hydroxyl value of the amine polyol is 350 mgKOH / g or more, there is an advantage that the strength of the polyurethane resin can be further improved. Moreover, there exists an advantage that the elongation property of the said polyurethane resin, ie, the softness | flexibility, becomes more excellent because it is 500 mgKOH / g or less.

The amine polyol can be used alone or in combination of two or more.

The amine polyol is preferably contained in the polyol composition in an amount of 1 to 13 parts by weight, and more preferably 3 to 10 parts by weight.
When the amine polyol is contained in the polyol composition in an amount of 1 part by weight or more, there is an advantage that the curability of the polyurethane resin and the impact resistance at a low temperature can be further improved. Further, the inclusion of 13 parts by weight or less has an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperatures.

The alkylene diol (c) is a saturated hydrocarbon diol having two primary hydroxyl groups in the molecule and having a freezing point of −20 ° C. or lower. That is, a diol having a freezing point of −20 ° C. or lower and two saturated hydroxyl groups bonded to a saturated hydrocarbon.
Specifically, the alkylene diol is a compound represented by HO—H ₂ C—R—CH ₂ —OH, R is a linear or branched saturated hydrocarbon, and the freezing point is −20. It is below ℃.
The freezing point of the alkylene diol (c) is measured at 1 atm by a method according to JIS K0065.

Examples of the alkylene diol (c) include alkylene diols having a branched saturated hydrocarbon, alkylene diols having a linear saturated hydrocarbon, and the like.

Specifically, examples of the alkylene diol having the branched saturated hydrocarbon include 2-methyl-1,3-propanediol (freezing point: -91 ° C.), 2-methyl-1,4-butanediol. (Freezing point: −30 ° C. or lower), 3-methyl-1,5-pentanediol (freezing point: −50 ° C. or lower), 2,4-diethyl-1,5-pentanediol (freezing point: −30 ° C. or lower), etc. Can be mentioned.
In addition, examples of the alkylene diol having the linear saturated hydrocarbon include 1,3-propanediol (freezing point: −28 ° C.).

The alkylene diol is preferably an alkylene diol having the above-mentioned branched saturated hydrocarbon in that the polyurethane resin has more excellent impact resistance at low temperatures, and 3-methyl-1,5-pentane is preferable. Diol or 2,4-diethyl-1,5-pentanediol is more preferable.

The alkylene diol has a hydroxyl value determined according to JIS K1557-1 (Method A) of preferably 300 to 1500 mgKOH / g, and more preferably 700 to 1000 mgKOH / g.
When the hydroxyl value of the alkylene diol is 300 mgKOH / g or more, there is an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperature. Moreover, there exists an advantage that the impact resistance in the low temperature of the said polyurethane resin can become more excellent because it is 1500 mgKOH / g or less.

The total number of carbon atoms in the molecule is not limited, but the total number of carbon atoms is preferably 4 to 10, and more preferably 6 to 9. That is, the alkylene diol is more preferably an alkylene diol having 6 to 9 carbon atoms and having a branched saturated hydrocarbon.

The alkylene diols can be used singly or in combination of two or more.

The alkylene diol is preferably contained in the polyol composition in an amount of 1 to 5 parts by weight, more preferably 1.5 to 2.0 parts by weight.
When the alkylene diol is contained in the polyol composition in an amount of 1 part by weight or more, there is an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperatures. In addition, the inclusion of 5 parts by weight or less has an advantage that the polyurethane resin can be more excellent in impact resistance at low temperatures.

The castor oil-based polyol (d) is a polyol having a castor oil fatty acid ester structure in the molecule.
By using the castor oil-based polyol (d), it is possible to suppress a decrease in deformation resistance at high temperatures and impact resistance at low temperatures of the polyurethane resin while lowering the viscosity of the polyol composition.

Examples of the castor oil-based polyol (d) include castor oil, castor oil derivative polyol synthesized using castor oil or castor oil fatty acid, and the like.

Examples of the castor oil derivative polyol include a polyol having a plurality of hydroxyl groups synthesized using castor oil and / or castor oil fatty acid.
More specifically, as the castor oil derivative, for example, an ester exchange reaction product of castor oil and polyol, an esterification reaction product of castor oil fatty acid and polyol, the ester exchange reaction product or the esterification reaction product is alkylene. Examples include polyols to which oxides are added.

The castor oil-based polyol preferably has an average hydroxyl value determined according to JIS K1557-1 (Method A) of 100 to 300 mgKOH / g.
When the average hydroxyl value of the castor oil-based polyol is 100 mgKOH / g or more, there is an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperature and impact resistance at low temperature. Moreover, there exists an advantage that the said polyol composition becomes a thing of a lower viscosity by being 300 mgKOH / g or less.

The castor oil-based polyol is preferably contained in the polyol composition in an amount of 10 to 20 parts by weight, more preferably 12 to 18 parts by weight.
When the castor oil-based polyol is contained in the polyol composition in an amount of 10 parts by weight or more, there is an advantage that the polyol composition has a lower viscosity. Moreover, when 20 parts by weight or less is contained, there is an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperature and impact resistance at low temperature.

The amine compound (e) having an active hydrogen-containing amino group in the molecule has an active hydrogen-containing amino group represented by —NH ₂ or ═NH in the molecule.

Examples of the amine compound (e) include an aliphatic amine compound having an aliphatic hydrocarbon and an active hydrogen-containing amino group in the molecule, or an aromatic hydrocarbon and an active hydrogen-containing amino group in the molecule. An aromatic amine compound etc. are mentioned.

Examples of the aliphatic amine compound include an aliphatic monoamine compound having one active hydrogen-containing amino group in the molecule and an aliphatic polyamine compound having a plurality of active hydrogen-containing amino groups in the molecule.
Specifically, examples of the aliphatic polyamine compound include ethylenediamine, hexamethylenediamine, and diethylenetriamine.

Examples of the aromatic amine compound include an aromatic monoamine compound having one active hydrogen-containing amino group in the molecule and an aromatic polyamine compound having a plurality of active hydrogen-containing amino groups in the molecule.

Specifically, examples of the aromatic monoamine compound include aniline.
Specific examples of the aromatic polyamine compound include toluenediamine, 4,4′-diamino-3,3′-diethyldiphenylmethane, and 3,5-diethyltoluenediamine.

The amine compound is preferably the aromatic polyamine compound, more preferably 3,5-diethyltoluenediamine, in that the polyurethane resin can be more excellent in curability and deformation resistance at high temperatures.

The amine compound is preferably contained in the polyol composition in an amount of 0.5 to 1.5 parts by weight, more preferably 0.8 to 1.0 parts by weight.
By including 0.5 parts by weight or more of the amine compound in the polyol composition, there is an advantage that the curability of the polyurethane resin and the deformation resistance at high temperature can be further improved. Moreover, it is suppressed that the reactivity when the said polyol composition reacts with the polyisocyanate compound mentioned later by containing 1.5 weight part or less is too high, The polyurethane resin obtained after such reaction There is an advantage that the surface of the substrate can be smoother.

Specific examples of the inorganic filler include powders such as calcium carbonate, quartz (crystalline silica), and alumina.

The inorganic filler is preferably contained in the polyol composition in an amount of 40 to 70 parts by weight, and more preferably 45 to 60 parts by weight.
By including 40 parts by weight or more of the filler in the polyol composition, there is an advantage that the polyurethane resin can be more excellent in deformation resistance at high temperatures. In addition, the inclusion of 70 parts by weight or less has an advantage that the polyurethane resin can be more excellent in impact resistance at low temperatures.

The polyol composition may contain a general catalyst for synthesizing a polyurethane resin in order to promote a reaction with a polyisocyanate compound described later.
Further, the polyol composition may contain a plasticizer in order to improve compatibility with the polyisocyanate compound described later.

Examples of the catalyst include a metal-based curing catalyst or an amine catalyst.
Examples of the metal-based curing catalyst include tin catalysts such as dibutyltin dilaurate, dioctyltin dilaurate and dibutyltin dioctate, lead catalysts such as lead octylate, lead octenoate and lead naphthenate, bismuth octylate, bismuth neodecanoate. And bismuth catalyst.
Examples of the amine catalyst include triethylamine, tripropylamine, tributylamine, N-methylmorpholine, N-ethylmorpholine, dimethylbenzylamine, N, N, N ′, N′-tetramethylhexamethylenediamine, N, N , N ′, N ′, N ″ -pentamethyldiethylenetriamine, bis- (2-dimethylaminoethyl) ether, triethylenediamine, dimethylethanolamine, N-trioxyethylene-N, N-dimethylamine, N, N-dimethyl -N-hexanolamine and the like.
The amount of the catalyst is appropriately adjusted.

The polyol composition can be produced by mixing the above-described blending components by a conventionally known general method. Specifically, for example, it can be produced by mixing each compounding component by hand stirring or using a general mixing apparatus.

Next, an embodiment of the polyurethane resin of the present invention will be described.

The polyurethane resin of the present embodiment is obtained by reacting the polyol composition with a polyisocyanate compound having a plurality of isocyanate groups in the molecule.

As the polyisocyanate compound, conventionally known general compounds can be mentioned.

Specifically, examples of the polyisocyanate compound include tetramethylene diisocyanate, dodecamethylene diisocyanate, hexamethylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, 2,4,4-trimethylhexamethylene diisocyanate, and lysine diisocyanate. Aliphatic polyisocyanates such as 2-methylpentane-1,5-diisocyanate and 3-methylpentane-1,5-diisocyanate.

Examples of the polyisocyanate compound include isophorone diisocyanate, hydrogenated xylylene diisocyanate, 4,4′-dicyclohexylmethane diisocyanate, 1,4-cyclohexane diisocyanate, methylcyclohexylene diisocyanate, and 1,3-bis (isocyanate methyl). Examples include alicyclic polyisocyanates such as cyclohexane.

Examples of the polyisocyanate compound include tolylene diisocyanate, 2,2′-diphenylmethane diisocyanate, 2,4′-diphenylmethane diisocyanate, 4,4′-diphenylmethane diisocyanate (MDI), and polymethylene polyphenyl polyisocyanate (polymeric). MDI), 4,4′-dibenzyl diisocyanate, 1,5-naphthylene diisocyanate, xylylene diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, dialkyldiphenylmethane diisocyanate, tetraalkyldiphenylmethane diisocyanate, α, α , Α, α-tetramethylxylylene diisocyanate and the like, and aromatic polyisocyanates having an aromatic ring in the molecule. That.

Furthermore, as the polyisocyanate compound, modified polyisocyanate compounds such as carbodiimide bodies, isocyanurate bodies, burette bodies, and adduct bodies of the above-described compounds can be used.

As the polyisocyanate compound, the aromatic polyisocyanate is preferable, and the polymethylene polyphenyl polyisocyanate is more preferable in terms of excellent reactivity with the polyol composition.

The polyisocyanate compound is preferably reacted so that an isocyanate group is 1.0 to 1.2 mol per 1 mol of active hydrogen groups in the polyol composition. When the isocyanate group is 1.0 mol or more with respect to 1 mol of active hydrogen groups in the polyol composition, there is an advantage that poor curing of the polyurethane resin, poor water resistance, or strength reduction can be suppressed. Further, when the isocyanate group is 1.2 mol or less, there is an advantage that the polyurethane resin is suppressed from foaming due to the reaction of excess isocyanate groups with moisture in the air.

The polyurethane resin can be produced by a general method. Specifically, for example, the polyol composition and the polyisocyanate compound can be mixed and cured for production. More specifically, for example, a film-like polyurethane placed on a steel material by placing the polyol composition and the polyisocyanate compound in a two-component mixed spray coating machine and coating the plate-like steel material surface. Resin can be manufactured.

The polyol composition or polyurethane resin of the above embodiment is as exemplified above, but the present invention is not limited to the above exemplified polyol composition or polyurethane resin.
Moreover, the various aspects used in a general polyol composition or a polyurethane resin can be employ | adopted in the range which does not impair the effect of this invention.

Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.

Hereinafter, details of raw materials for producing the polyol composition will be described.

(A) Polybutadiene polyol (a-1) Polybutadiene polyol having an average hydroxyl value of 47 mg KOH / g (trade name “Poly bd R-45 HT” manufactured by Idemitsu Kosan Co., Ltd.)
(A-2) Polybutadiene polyol having an average hydroxyl value of 103 mg KOH / g (trade name “Poly bd R-15 HT” manufactured by Idemitsu Kosan Co., Ltd.)
(B) Amine polyol (b-1) Amine polyol obtained by adding 3 mol of propylene oxide to aniline (average hydroxyl value: 420 mgKOH / g)
(B-2) Amine polyol obtained by adding 2 moles of butylene oxide to aniline (average hydroxyl value: 473 mgKOH / g)
(C) an alkylene diol in which two primary hydroxyl groups are bonded via a saturated hydrocarbon and the number of carbon atoms connecting the two primary hydroxyl groups is an odd number. (C-1) 3-methyl-1,5-pentanediol (Hydroxyl value: 951 mg KOH / g Freezing point: −50 ° C. or less)
(C-2) 2,4-diethyl-1,5-pentanediol (hydroxyl value: 700 mg KOH / g freezing point: -30 ° C. or less)
(D) Castor oil-based polyol (d-1) Castor oil derivative polyol (polyester polyol derived from castor oil)
(Product name “URIC-Y403” manufactured by Ito Oil Co., Ltd.)
(Hydroxyl value: 160 mgKOH / g)
(E) Amine compound having an active hydrogen-containing amino group in the molecule (e-1) 3,5-diethyltoluenediamine Other raw materials 1,3-butanediol (one primary hydroxyl group)
(Hydroxyl value: 1247 mg KOH / g Freezing point: -50 ° C or less)
1,6-hexanediol (hydroxyl value: 9950 mg KOH / g freezing point: 42 ° C.)
Trimethylolpropane (Hydroxyl value: 1256 mgKOH / g Freezing point: 58 ° C)
・ Inorganic filler Quartz (Crystalline silica) (Brand name “Bird roof quartzite” manufactured by Marues)

(Examples 1 to 5, Comparative Examples 1 to 5)
According to the blending amount shown in Table 1, after mixing raw materials other than the inorganic filler, a polyol composition was produced by further adding and mixing the inorganic filler.

<Measurement of average hydroxyl value>
The average hydroxyl value of the mixture after mixing raw materials other than the inorganic filler was determined according to JIS K1557-1 (Method A). The results are shown in Table 1.

<Evaluation of storage stability>
Each of the produced polyol compositions was allowed to stand at −5 ° C. for 7 days, where “O” indicates no cloudiness or precipitation, and “X” indicates that cloudiness or precipitation is observed. The results are shown in Table 1.

Subsequently, the polyol composition and the following polyisocyanate so that the isocyanate group of the polyisocyanate compound is 1.08 mol with respect to 1 mol of active hydrogen groups in the polyol composition produced in each example and each comparative example. The compound and the following catalyst were mixed to produce a polyurethane resin. Specifically, using a two-component mixed spray coating machine, a two-component mixture was applied to a plate-like steel material having a thickness of 5 mm to produce a polyurethane resin coating film having a thickness of 2.5 mm.
Polyisocyanate compound Polymethylene polyphenyl polyisocyanate (free NCO group content: 31% by weight,
Product name "Millionate MR-100" manufactured by Nippon Polyurethane Industry Co., Ltd.)
Catalyst Dioctyltin dilaurate (0.02 parts by weight with respect to 100 parts by weight of polyol composition)

<Evaluation of polyurethane resin coating film>
Each coating film of the polyurethane resin was evaluated by the method shown below. As shown below, the evaluation items were curability, deformability against indentation, and impact resistance. The evaluation results are shown in Table 2.
-Curability The surface of the coating film after 24 hours of coating was confirmed, and the presence or absence of tack was confirmed.
・ Deformability against indentation (60 ℃)
Evaluation was made according to the British standard BS EN10290: 2002, and the indentation length at 60 ° C. was 30% or less (0.75 mm or less) with respect to the film thickness, and the one exceeding 30% was rated as x.
・ Impact resistance (-30 ℃)
Samples that were allowed to stand at −30 ° C. for 2 hours were evaluated according to British Standard BS EN10290: 2020. Specifically, an impact was applied to the sample, and a check was made with a holiday detector (pinhole detector) at 15 kV.

The composition for polyurethane resin of the present invention is suitably used as a main component of a so-called two-component reactive polyurethane resin paint, for example. In addition, the polyurethane resin produced using the polyurethane resin composition of the present invention is excellent in impact resistance at low temperatures and suppressed in deformation at high temperatures. For example, steel material protection for protecting steel materials such as steel pipes. It can be used in applications such as materials.

Claims

A polybutadiene polyol (a) having a polybutadiene structure and a plurality of hydroxyl groups in the molecule, an amine polyol (b) which is a tertiary amine having a plurality of hydroxyl groups in the molecule, and having two primary hydroxyl groups in the molecule and a freezing point And an alkylene diol (c) having a temperature of −20 ° C. or lower.
The polyol composition according to claim 1, further comprising a castor oil-based polyol (d).
Furthermore, the polyol composition of Claim 1 or 2 containing the amine compound (e) which has an active hydrogen containing amino group in a molecule | numerator.
A polyurethane resin obtained by reacting the polyol composition according to any one of claims 1 to 3 with a polyisocyanate compound having a plurality of isocyanate groups in the molecule.