US20030149214A1

US20030149214A1 - Polyurethanes with improved tear propagation resistance

Info

Publication number: US20030149214A1
Application number: US09/379,938
Authority: US
Inventors: Alfred Westfechtel; Roland Gruetzmacher; Rainer Hoefer
Original assignee: Alfred Westfechtel; Roland Gruetzmacher; Rainer Hoefer
Current assignee: BASF Personal Care and Nutrition GmbH
Priority date: 1994-08-18
Filing date: 1999-08-24
Publication date: 2003-08-07
Also published as: US6610811B1

Abstract

Disclosed are polyurethanes formed from (A) a polyol component containing dimeric diol and/or trimeric triol and/or a polyether containing dimeric diol units and/or a polyester with OH-terminal groups formed from polcarboxylic acids, preferably dimeric fatty acids or trimeric fatty acids and diols; and (B) an isocyanate component containing prepolymers obtainable from the reaction between polyfunctional isocyanates and dimeric diol and/or trimeric triol and/or a polyether containing dimeric diol units and/or a polyester with OH-terminal groups formed from polycarboxylic acids, preferably dimeric fatty acids or trimeric fatty acids and diols; at least one of the components (A) and (B) contain dimeric or trimeric fatty acid or dimeric or trimeric fatty alcohol. The proposed polyurethanes have excellent resistance to tear propagation.

Description

FIELD OF THE INVENTION

This invention relates to polyurethanes with improved tear propagation resistance which contain dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid and/or trimer fatty acid, and diols.

PRIOR ART

Dimeric fatty alcohols (dimer diols) have been known for some time.

DE-A1 11 98 348, for example, describes their production by dimerization of unsaturated fatty alcohols with basic alkaline earth metal compounds at temperatures above 280° C.

They may also be obtained by hydrogenation of dimeric fatty acids and/or esters thereof in accordance with DE-B-17 68 313.

Another method of producing dimer diols comprises dimerizing unsaturated alcohols in the presence of silica/alumina catalysts and basic alkali metal compounds (cf. International patent application WO 91/13918).

A certain amount of trimerized fatty acid is always formed in the production of dimer fatty acid. This trimer fatty acid can be concentrated by removing the dimer fatty acid by distillation. After esterification with methanol for example, the esters of the trimer fatty acid—similarly to the esters of the dimer fatty acid—can be hydrogenated to trimer triol. This trimer triol, a trihydric alcohol containing 54 carbon atoms, may also be used in accordance with the present invention.

It is also known from unpublished German patent application P 43 16 245.2 that dimer diol can be condensed in the presence of an acid with elimination of water to form a polyether containing dimer diol units.

Polyurethanes containing dimer diol or trimer triol are also known.

The use of dimeric and trimeric fatty alcohols and mixtures thereof in the production of polyurethanes is known from DE-B1 11 79 660 which relates to the production of sulfur-containing elastic coating compositions.

It is also known that dimer diol can be used as a polyol for the production of polyurethane coatings by reaction with diisocyanates. Thus, DE-A1 12 25 795 describes polyurethane paints of dimeric and/or trimeric fatty alcohols containing an average number of 36 or 54 carbon atoms.

EP-B10 199 609 describes polyurethane adhesive layers produced from an NCO-terminated prepolymer based on polyester or polyether diols and dimer diol as chain-extending agent.

Polyurethane dispersions containing dimer diol and their use for stoving lacquers are described in DE-A1 42 37 965.

Unpublished German patent application P 43 08 100.2 describes casting resins of which the hydrolysis stability is improved by the addition of dimer diol.

The problem addressed by the present invention was to provide polyurethanes having improved tear propagation resistance.

It has surprisingly been found that polyurethanes containing dimer diol, trimer triol or dimer fatty acid or trimer fatty acid units show excellent tear propagation resistance.

DESCRIPTION OF THE INVENTION

The present invention relates to polyurethanes having improved tear propagation resistance which are produced from

A) a polyol component containing dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid and/or trimer fatty acid, and diols and

B) an isocyanate component containing prepolymers obtainable by reacting polyfunctional isocyanates with dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid and/or trimer fatty acid, and diols, at least one of components A or B containing dimer or trimer fatty acid or dimer or trimer fatty alcohol as a constituent.

The polyol component contains dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid and/or trimer fatty acid, and diols.

Irrespective of the processes described at the beginning for the production of the dimer diols, dimer diols produced from fatty acids or esters thereof or fatty alcohols containing 18 carbon atoms are preferably used. Dimer diols containing 36 carbon atoms are formed in this way. Dimer diols which have been produced by the industrial processes mentioned above always contain varying amounts of trimer triols and monohydric alcohols. In general, their percentage dimer diol content exceeds 70% by weight, the rest being trimer triols and monomer alcohols. Both these dimer diols and also purer dimer diols containing more than 90% by weight of dimer diol may be used in accordance with the present invention. Dimer diols containing more than 90 to 99% by weight of dimer diol are particularly preferred. Of these dimer diols, those with at least partly or completely hydrogenated double bonds are preferred.

Similarly to the esters of dimer fatty acid, the esters of trimer fatty acid may be hydrogenated to trimer triol. This trimer triol, a trihydric alcohol containing 54 carbon atoms, may also be used in accordance with the present invention. The trimer alcohol contains at least 50% by weight and preferably at least 65% by weight of trihydric alcohol.

The dimer diol or the trimer diol have hydroxyl values of 180 to 215 and preferably 200 to 210.

The polyethers containing dimer diol units may be produced in accordance with unpublished German patent application P 43 16 245.2 by acid-catalyzed polycondensation of suitable low molecular weight alkylene glycols at elevated temperature.

The polyethers containing dimer diol units have a hydroxyl value (OHV) of less than 175 and, more particularly, in the range from 10 to 100. The OH value expresses the quantity of KOH in mg which is equivalent to the quantity of acetic acid bound by 1 g of substance in the acetylation reaction.

The polyethers containing dimer diol units are liquid at room temperature (20° C.), i.e. they have a Brookfield viscosity at 25° C. of >3,000 mPas and, more particularly, in the range from 3,800 to 12,000 mpas.

The polyethers containing dimer diol units are hydrophobic, i.e. they are substantially insoluble in water at 20° C., preferably less than 1 mg and, more preferably, less than 0.1 mg dissolving in 100 ml of water.

Polyethers containing dimer diol units in the context of the invention also include the alkoxylation products of dimer diol or trimer triol which are obtainable by reaction of the hydroxyl groups of dimer diol or trimer triol with ethylene oxide, propylene oxide or butylene oxide. These polyethers may contain 1 to 20 and preferably 3 to 10 moles of alkylene oxide per mole of dimer diol or trimer triol.

Another embodiment is characterized by the use of OH-terminated polyesters obtained by esterification of polycarboxylic acids, preferably dimer or trimer fatty acid, with diols. Examples of suitable diols are ethylene glycol, diethylene glycol, propylene glycol, neopentyl glycol, hexane-1,6-diol and butane-1,4-diol.

In the reaction of dicarboxylic acids, particularly dimer fatty acid, with diols, the equivalent ratio of OH to COOH is generally between 1.4:1 and 3:1 and preferably between 1.8:1 and 2.2:1. In the reaction of tricarboxylic acids, particularly trimer fatty acid, with diols, the equivalent ratio of OH to COOH is generally between 2.5:1 and 4:1 and preferably between 2.7:1 and 3.3:1.

50 to 100% by weight and preferably 70 to 90% by weight of the polyol component of the polyurethanes according to the invention consists of dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid and/or trimer fatty acid, and diols, the rest consisting of another polyol typically encountered in polyurethane chemistry.

These other polyols may be polyether, polyester or oleochemical polyols or mixtures of these compounds. An overview of polyethers and polyesters typically encountered in polyurethane chemistry can be found, for example, in Ullmanns Enzyklopädie der technischen Chemie, 4th Edition, Vol. 19, Verlag Chemie, Weinheim, pages 304-5.

Examples of suitable hydroxyl-terminated polyesters are polyesters based on polycarboxylic acids, such as adipic acid, phthalic acid, maleic acid and azelaic acid, and diols, such as ethylene glycol, propylene glycol, neopentyl glycol, hexane-1,6-diol and butane-1,4-diol.

The polymeric reaction products of dimer or trimer fatty acids with polyhydric alcohols, for example ethylene glycol, propylene glycol, neopentyl glycol, hexane-1,6-diol and butane-1,4-diol, are also suitable.

Polycaprolactones and polycarbonates are preferred.

Examples of suitable hydroxyl-terminated polyethers are polyethylene glycol, polypropylene glycol and—preferably—polytetrahydrofuran.

Another group of preferred polyols are the oleochemical polyols.

Oleochemical polyols are understood to be polyols based on natural oils and fats, for example the reaction products of epoxidized fatty compounds with monohydric, dihydric or polyhydric alcohols or glycerol esters of long-chain fatty acids which are at least partly substituted by hydroxyl groups.

A subsidiary group of these compounds are the ring-opening products of epoxidized triglycerides, i.e. epoxidized fatty acid glycerol esters which have been ring-opened with the ester bonds intact. The ring-opening products may be produced from a number of epoxidized triglycerides of vegetable or animal origin. For example, epoxidized triglycerides containing 2 to 10% by weight of epoxide oxygen are suitable. Products such as these may be obtained from a number of fats and oils, for example beef tallow, palm oil, peanut oil, rapeseed oil, cottonseed oil, soybean oil, sunflower oil and linseed oil, by epoxidation of the double bonds. Particularly preferred epoxidized triglycerides are epoxidized soybean oil and epoxidized linseed oil.

Suitable alcohols for the ring-opening of the epoxidized triglycerides are methanol, ethanol, propanol, isopropanol, butanol, hexanol, 2-ethylhexanol, fatty alcohols containing 6 to 22 carbon atoms, cyclohexanol, benzyl alcohol, ethane-1,2-diol, propane-1,2-diol, propane-1,3-diol, butane-1,4-diol, hexane-1,6-diol, neopentyl glycol, trimethylol propane, glycerol, trimethylol ethane, pentaerythritol, sorbitol and hydroxy compounds containing ether groups, such as alkyl glycols, or oligomeric glycols and oligomeric glycerols.

The ring-opening reaction of epoxidized fatty acid esters or triglycerides with an alcohol may optionally be followed by transesterification with the starting material or with other triglycerides subsequently added, for example palm oil, peanut oil, rapeseed oil, cottonseed oil, soybean oil, sunflower oil and linseed oil. Corresponding oleochemical polyols are described, for example, in German patent application DE-A1 41 28 649.

Another group of oleochemical polyols are ring-opening and transesterification products of epoxidized fatty acid esters of lower alcohols, i.e. epoxidized fatty acid methyl, ethyl, propyl or butyl esters. The ring-opening or transesterification products with dihydric to tetrahydric alcohols are preferred, the reaction products with ethylene glycol, propylene glycol, oligomeric ethylene glycols, oligomeric propylene glycols, glycerol, trimethylol propane or pentaerythritol being particularly preferred. These products may be produced by known epoxidation or ring-opening methods, the transesterification optionally being carried out during or after the ring-opening step by removal of the lower alcohol from the reaction equilibrium. Preferred ring-opening and transesterification products are those where a molar ratio of epoxidized fatty acid ester to the alcohol used for the reaction of 1:1 to 1:10 has been applied.

The oleochemical polyols also include the reaction products of epoxidized fatty alcohols with C _2-8alcohols having a functionality of 1 to 10 and, more particularly, 2 to 4, the molar ratio of the epoxide groups to the hydroxyl groups being 1:1 to 1:10.

The Oleochemical polyols obtainable by the transesterification of dihydric or polyhydric alcohols, for example the adduct of ethylene oxide or propylene oxide with glycerol, with triglycerides, for example palm oil, peanut oil, rapeseed oil, cottonseed oil, soybean oil, sunflower oil and linseed oil, may also be used in accordance with the present invention.

The hydroxyl values of the other polyols as measured in accordance with DIN 53240 are in the range from 5 to 600, preferably in the range from 20 to 300 and more preferably in the range from 50 to 200.

The isocyanate component of the polyurethanes according to the invention contains an NCO-terminated prepolymer obtainable by reaction of polyfunctional isocyanates with dimer diol and/or trimer diol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from a polycarboxylic acid, preferably a dimer fatty acid or trimer fatty acid, and diols.

The polyfunctional isocyanate has a functionality of 2 to 4 and preferably 2. Suitable polyfunctional isocyanates are both aromatic and aliphatic, monocyclic and polycyclic polyfunctional isocyanate compounds.

Examples of such polyfunctional isocyanates are toluene 2,4-diisocyanate, toluene 2,6-diisocyanate, diphenyl methane 4,4′-diisocyanate, m-xylylene diisocyanate, 3-isocyanatomethyl-3,5,5-trimethyl cyclohexyl isocyanate, 1,6-hexane diisocyanate, naphthylene 1,5-diisocyanate and toluene 2,4,6-triisocyanate.

Diphenyl methane 4,4′-diisocyanate is particularly preferred.

In the production of the prepolymers, the equivalent ratio of NCO to OH is generally between 6:1 and 1.5:1 and preferably between 3:1 and 2:1.

50 to 100% by weight and preferably 70 to 90% by weight of the isocyanate component of the polyurethanes according to the invention consists of the prepolymers.

Besides the prepolymers, the isocyanate component may also contain other polyfunctional isocyanate compounds. An overview of polyisocyanates typically used in polyurethane chemistry can be found, for example, in Ullmanns Enzyklopädie der technischen Chemie, 4th Edition, Vol. 19, Verlag Chemie, Weinheim, page 303.

Preferred polyisocyanates are aromatic diisocyanates, such as diphenyl methane diisocyanate or toluene diisocyanate and, in particular, technical diphenyl methane diisocyanate which contains isocyanates having a functionality of more than 2 and which is marketed, for example, under the name of Desmodur® VKS-H by Bayer AG.

In the production of the polyurethanes from components A and B, the equivalent ratio of NCO groups to OH groups (NCO:OH) is generally between 1.2:1 and 0.8:1 and preferably between 1.05:1 and 0.95:1.

In addition, the polyurethanes may contain various auxiliaries which are preferably incorporated in the polyol. Fillers, for example, may be used. Suitable fillers are inorganic compounds non-reactive to isocyanates, for example chalk or gypsum, precipitated silicas, zeolites, bentonites, ground minerals and other inorganic fillers known to the expert active in the field in question. Organic fillers, more particularly chopped fibers and others, may also be used. Fillers which make the polyurethanes thixotropic are preferred.

The polyurethanes according to the invention may also contain accelerators. Suitable accelerators are, for example, tertiary bases, such as bis-(N,N-dimethylamino)-diethyl ether, dimethylaminocyclohexane, N,N-dimethylbenzyl amine, N-methyl morpholine and the reaction products of dialkyl-(β-hydroxyethyl)-amine with monoisocyanates and esterification products of dialkyl-(β-hydroxyethyl)-amine and dicarboxylic acids. Another important accelerator is 1,4-diaminobicyclo-(2.2.2)-octane. Non-basic substances may also be used as accelerators. Examples of suitable non-basic accelerators are metal compounds, for example iron pentacarbonyl, iron acetyl acetonate and tin(II) (2-ethylhexoate), dibutyl tin dilaurate or molybdenum glycolate.

The polyurethanes according to the invention are produced by mixing components A and B. In general, this is done immediately before use, pending which the two components are stored separately in the absence of moisture.

In one preferred embodiment, the polyurethanes according to the invention have a tear propagation resistance according to DIN 53515 above 10 Nmm ⁻¹and, more particularly, above 15 Nmm⁻¹.

The polyurethanes according to the invention may be used as sealing compounds, for example in the electrical industry and in the building industry.

The polyurethanes according to the invention may also be used as adhesives and casting resins.

EXAMPLES

All percentages are by weight, unless otherwise indicated. [0060]
Starting Compounds:[0061]
Dimer diol—Sovermol® POL 900: OH value 203, dimer content>90% [0062]
Trimer triol—Sovermol® POL 930: OH value 203, trimer content>50% by weight [0063]

Example 1

Production of the NCO-Terminated Prepolymers [0064]
The quantity of polyol required for the theoretically calculated NCO value is added dropwise with stirring to a liquid polyisocyanate over a period of about 2 h at room temperature in an inert gas atmosphere. The reaction mixture is then heated at 80° C. until there is no further reduction in the NCO value. Prepolymers A to C were obtained in the same way. [0065]
1. Production of Prepolymer A [0066]
33.2% by weight of trimer triol [0067]
66.8% by weight of diphenyl methane 4,4′-diisocyanate [0068]
end product: 16.4% NCO [0069]
Brookfield viscosity (25° C.): 8,240 mPa/s [0070]
2. Production of Prepolymer B [0071]
33.2% by weight of dimer diol [0072]
66.8% by weight of diphenyl methane 4,4′-diisocyanate [0073]
end product: 16.8% NCO [0074]
Brookfield viscosity (25° C.): 2,270 mPa/s [0075]
3. Production of Prepolymer C (Comparison Example) [0076]
37.68% by weight of polypropylene glycol (PPG 1025, a DOW product, OH value 102) [0077]
62.32% by weight of diphenyl methane 4,4′-diisocyanate [0078]
end product: 17.0% NCO [0079]
Brookfield viscosity (25° C.): 2,500 mPa/s [0080]

Example 2 (General Procedure)

The NCO-terminated prepolymers (A to C) prepared in accordance with Example 1 are cast in equimolar quantities with the following hydroxyl components with addition of 5% of zeolite (Baylith® L, Bayer AG) and the tear propagation resistance is measured in accordance with DIN 53515. [0081]

Polyurethanes 2 a-i listed in Table 1 were obtained in the same way.

TABLE 1


			Tear propagation
			resistance accord-
			ing to DIN 53515
Example	Prepolymer	Hydroxyl component	[Nmm⁻¹]

a	A	Trimer triol	26.4
b	B	Sovermol ® POL 900	18.4
c	B	Dimer diol, 76%	11.8
d	B	Dimer diol, 68%	6.4
e	B	Sovermol ®650 NS	4.6
f	B	Lin. polyester diol	5.5
g	A	Castor oil	5.5
h	C	Castor oil	5.5
i	C	Trimer triol	6.3

The linear polyester diol is a polyester of diethylene glycol, neopentyl glycol, hexane-1,6-diol and adipic acid with an OH value of 60. [0083]
Sovermol® 650 NS is a dimer diol with a dimer content of 68% obtainable by the dimerization of unsaturated fatty alcohol. [0084]
Examples 2a to 2c correspond to the invention. [0085]
Examples 2d and 2e show that the tear propagation resistance decreases with the dimer content of the dimer diol. [0086]
Examples 2f to 2i show that particularly high tear propagation resistances are linked to the presence of dimer diol or trimer triol in the isocyanate component and the hydroxyl component. [0087]

Claims

1. Polyurethanes having improved tear propagation resistance characterized in that the polyurethanes are produced from

A) a polyol component containing dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid or trimer fatty acid and diols and

2. Polyurethanes as claimed in claim 1, characterized in that the polyol component contains at least 50% by weight—based on the polyol component—of dimer diol and/or trimer triol and/or a polyether containing dimer diol units and/or an OH-terminated polyester produced from polycarboxylic acids, preferably dimer fatty acid and/or trimer fatty acid, and diols.

3. Polyurethanes as claimed in claims 1 and 2, characterized in that the isocyanate component contains at least 50% by weight—based on the isocyanate component—of prepolymers.

4. Polyurethanes as claimed in claims 2 to 3, characterized in that the other polyols of the polyol component are selected from the group consisting of polyethers, polyesters and oleochemical polyols.

5. Polyurethanes as claimed in claims 2 to 4, characterized in that the other isocyanates of the isocyanate component are aromatic diisocyanates, preferably diphenyl methane diisocyanate and, in particular, technical diphenyl methane diisocyanate with a functionality of more than 2 or toluene diisocyanate.

6. Polyurethanes as claimed in claims 1 to 5, characterized in that an equivalent ratio of NCO to OH of 1.2:1 to 0.8:1 and preferably 1.05:1 to 0.95:1 is maintained during production of the polyurethane.

7. Polyurethanes as claimed in claims 1 to 6, characterized in that they have a tear propagation resistance above 10 Nmm⁻¹and, more particularly, above 15 Nmm⁻¹.

8. The use of the polyurethanes claimed in claims 1 to 7 as sealing compounds.