Patent Application
20170029552
The present invention relates to compositions for producing transparent polythiourethane articles containing or consisting of
The invention further relates to a process for producing transparent polythiourethane articles by reaction of such a composition and to the thus manufactured polythiourethane articles and also to the use of aromatic nitriles for producing transparent polythiourethane articles and, in addition, to a mixture of a polyisocyanate and an aromatic nitrile for producing compact transparent polythiourethane articles.
For various applications, for example as a lightweight substitute for mineral glass for producing panes for automobile and aircraft construction or as embedding compositions for optical, electronic or optoelectronic components, there is increasing interest on the market today in transparent, lightfast polyurethane compositions.
Particularly for high-quality optical applications, for example for lenses or spectacle glasses, there is generally a desire for plastics materials exhibiting high refraction coupled with low dispersion (high Abbe number).
The production of transparent polyurethane masses having a high refractive index has been described many times already. Araliphatic diisocyanates, i.e. diisocyanates whose isocyanate groups are bonded via aliphatic radicals to an aromatic system, are often used as polyisocyanate components. Owing to their aromatic structures, araliphatic diisocyanates afford polyurethanes having an increased refractive index while at the same time the aliphatic isocyanate groups guarantee the lightfastness and low yellowing tendency required for high-quality applications.
U.S. Pat. No. 4,680,369 and U.S. Pat. No. 4,689,387 describe polyurethanes/polythhiourethanes suitable as lens materials for example, the production of which involves combining special sulfur-containing polyols or mercapto-functional aliphatic compounds with monomeric araliphatic diisocyanates, for example 1,3-bis(isocyanatomethyl)benzene (m-xylylene diisocyanate, m-XDI), 1,4-bis(isocyanatomethyl)benzene (p-xylylene diisocyanate, p-XDI), 1,3-bis(2-isocyanatopropan-2-yl)benzene (m-tetramethylxylylene diisocyanate, m-TMXDI) or 1,3-bis(isocyanatomethyl)-2,4,5,6-tetrachlorobenzene, in order to achieve particularly high refractive indices.
Monomeric araliphatic diisocyanates such as m- and p-XDI or m-TMXDI are also mentioned in numerous further publications, for example EP-A 0 235 743, EP-A 0 268 896, EP-A 0 271 839, EP-A 0 408 459, EP-A 0 506 315, EP-A 0 586 091 and EP-A 0 803 743, as the preferred polyisocyanate component for producing high refractivity lens materials. They serve as crosslinker components for polyols and/or polythiols and, depending on the coreactant, afford transparent plastics having high refractive indices in the range from 1.56 to 1.67 and comparatively high Abbe numbers up to 45.
A substantial disadvantage of the mentioned processes for producing high refractivity polyurethanes/polythiourethanes for optical applications is that the reaction between polythiols and polyisocyanates is highly sensitive to impurities with the result that some of the manufactured lenses do not always meet the desired standards in terms of their transparency and freedom from cloudiness. This applies especially to application in lenses and the like.
The present invention accordingly has for its object to specify a composition for producing transparent polythiourethane articles which makes it possible to manufacture such articles with improved optical properties, in particular improved transparency and freedom from cloudiness.
This object is achieved in a composition of the type mentioned at the outset when the composition further contains D) at least one aromatic nitrile.
The present invention accordingly provides a composition for producing transparent polythiourethane articles containing or consisting of
In the context of the present invention, the term “transparent” is to be understood as meaning that the transparent article has a transmittance of ≧85% for a thickness of 2 mm and standard light type D65 (defined in DIN 6173). However, this transmittance value can deviate from the aforementioned value of ≧85% in the case of optional co-use of UV stabilizers and dyes.
The present invention is based on the finding that the presence of at least one aromatic nitrile in compositions of the type described at the outset has the result that in further processing to afford polythiourethanes the thus manufactured molded articles suffer from cloudiness much less frequently. Without wishing to be bound to a particular theory it is believed that the nitriles may either react with the thiols or act as solubility promoters for dimers or trimers of the polyisocyanate that are being formed. Without the nitrile these could precipitate which could be a possible reason for the cloudiness that occurs.
A further advantage is that the composition according to the invention is less sensitive to entrained water than prior art systems as are described in U.S. Pat. No. 8,044,165 B2 for example. Normally, the thiol component in particular must be dried to remove excess water which could otherwise impair the optical properties of manufactured optical components. By contrast this is not necessary for the present invention. Thus the water content of the thiol component in the compositions according to the invention may be >600 ppm, in particular >800 ppm or even more than 900 ppm.
There are various options for introducing the aromatic nitrile into the composition. The nitrile addition may preferably be effected during formulation of the composition, it being particularly preferable when the nitrile is premixed with the polyisocyanate component before the reaction with the thiol component is effected. However, the invention is in no way limited to this option. Thus, nitrile addition may also be effected before or during manufacture of the polyisocyanate which is typically effected by a liquid-phase or gas-phase phosgenation of the corresponding polyamines. The addition of portions of the aromatic nitrile at any desired timepoints is also possible.
It is further possible to add portions or the total amount of the aromatic nitriles only during mixing of the reactive components or to premix said portions or entirety with the thiol component.
It is also possible—aside from the previously described active addition of the aromatic nitriles—to manufacture a portion or else the total amount of aromatic nitriles in situ. This is achieved via a gas-phase phosgenation of araliphatic polyamines to afford the corresponding araliphatic polyisocyanates. Unlike liquid-phase phosgenation this forms aromatic nitriles as byproducts of the phosgenation. This option is very preferably applied in the gas-phase phosgenation of 1,3-xylylenediamine (1,3-XDA) and/or 1,4-xylylenediamine (1,4-XDA) to afford 1,3-bis(isocyanatomethyl)benzene (1,3-XDI) and/or 1,4-bis(isocyanatomethyl)benzene (1,4-XDI). Depending on the desired nitrile amount the thus manufactured araliphatic diisocyanate or a mixture of the compounds mentioned with the production-dependent amount of aromatic nitriles present may be employed in a composition according to the invention or else the nitrile amount may be increased by addition of further aromatic nitriles which may be identical or different to the nitriles present.
In principle the compositions according to the invention may contain not only the aromatic nitriles but, in addition, also other organic nitriles, for example aliphatic, cycloaliphatic or araliphatic nitriles.
The invention provides that the polyisocyanate component contains at least one polyisocyanate having at least two isocyanate groups per molecule, in particular from 2 to 6, preferably from 2 to 4, particularly preferably from 2 to 3. It is also possible to employ mixtures of polyisocyanates of different functionality and odd-numbered average functionalities may therefore arise. In the context of the present invention the term polyisocyanate is to be understood as meaning organic isocyanates having two or more free isocyanate groups. The polyisocyanate may be in monomeric form or else in oligomeric form. Modification reactions suitable therefor are for example the customary processes for catalytic oligomerization of isocyanates to form uretdione, isocyanurate, iminooxadiazinedione and/or oxadiazinetrione structures or for biuretization of diisocyanates such as are described by way of example in Laas et al., J. Prakt. Chem. 336, 1994, 185-200, in DE-A 1 670 666 and in EP-A 0 798 299 for example. Specific descriptions of such poly-isocyanates based on araliphatic diisocyanates may also be found in EP-A 0 081 713, EP-A 0 197 543, GB-A 1 034 152 and JP-A 05286978 for example. The syllable “poly” accordingly relates essentially to the number of isocyanate groups per molecule and does not necessarily mean that the polyisocyanate must have an oligomeric, much less a polymeric, structure.
Polyisocyanates that may be employed in the context of the present invention in principle include all polyisocyanates known per se. These are for example polyisocyanates in the molecular weight range 140 to 400 g/mol, for example 1,4-diisocyanatobutane, 1,5-diisocyanatopentane, 1,6-diisocyanatohexane (HDI), 1,5-diisocyanato-2,2-dimethylpentane, 2,2,4- or 2,4,4-trimethyl-1,6-diisocyanatohexane, 1,8-diisocyanatooctane, 1,9-diisocyanatononane, 1,10-diisocyanatodecane, 1,3- and 1,4-diisocyanatocyclohexane, 1,4-diisocyanato-3,3,5-trimethylcyclohexane, 1,3-diisocyanato-2-methylcyclohexane, 1,3-diisocyanato-4-methylcyclohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate; IPDI), 1-isocyanato-1-methyl-4(3)-isocyanatomethylcyclohexane, 2,4′- and 4,4′-diisocyanatodicyclohexylmethane (H12-MDI), 1,3- and 1,4-bis(isocyanatomethyl)cyclohexane, 2,5-bis(isocyanatomethyl)bicyclo[2.2.1]heptane, 2,6-bis(isocyanatomethyl)bicyclo[2.2.1]heptane, 4,4′-diisocyanato-3,3′-dimethyldicyclohexylmethane, 4,4′-diisocyanato-3,3′,5,5′-tetramethyldicyclohexylmethane, 4,4′-diisocyanato-1,1′-bi(cyclohexyl), 4,4′-diisocyanato-3,3′-dimethyl-1,1′-bi(cyclohexyl), 4,4′-diisocyanato-2,2′,5,5′-tetramethyl-1,1′-bi(cyclohexyl), 1,8-diisocyanato-p-menthane, 1,3-diisocyanatoadamantane, 1,3-dimethyl-5,7-diisocyanatoadamantane, 1,3- and 1,4-bis(isocyanatomethyl)benzene, 1,3- and 1,4-bis(1-isocyanato-1-methylethyl)benzene (TMXDI), bis(4-(1-isocyanato-1-methylethyl)phenyl) carbonate, phenylene 1,3- and 1,4-diisocyanate, tolylene 2,4- and 2,6-diisocyanate and any desired mixtures of these isomers, diphenylmethane 2,4′- and/or 4,4′-diisocyanate and naphthylene 1,5-diisocyanate and any desired mixtures of such diisocyanates.
These polyisocyanates may have been produced by any desired processes, for example by phosgenation of the corresponding amines in the gas or liquid phase but also by phosgene-free methods, for example by carbamate cleavage.
The polyisocyanates are preferably selected from 1,3-bis(isocyanatomethyl)benzene (1,3-XDI), 1,4-bis(isocyanatomethyl)benzene (1,4-XDI), 2,5-bis(isocyanatomethyl)bicyclo[2.2.1]heptane, 2,6-bis(isocyanatomethyl)bicyclo[2.2.1]heptane, 1,4-bis(isocyanatomethyl)cyclohexane, 1,3-bis(isocyanatomethyl)cyclohexane, 2,2′-diisocyanatodicyclohexylmethane, 2,4′-diisocyanatodicyclohexylmethane, 4,4′-diisocyanatodicyclohexylmethane (H12-MDI), 1-isocyanato-3,3,5-trimethyl-5-isocyanato ethylcyclohexane (isophoronediisocyanate; IPDI) or mixtures thereof, especially preferably 1,3-bis(isocyanatomethyl)benzene (1,3-XDI) and/or 1,4-bis(isocyanatomethyl)benzene (1,4-XDI). These poly- and diisocyanates are preferred because they make it possible to obtain lens materials having particularly good optical properties, such as a high refractive index and high transparency. These advantages are particularly pronounced for the diisocyanates mentioned as preferable 1,3-bis(isocyanatomethyl)benzene (1,3-XDI) and 1,4-bis(isocyanatomethyl)benzene (1,4-XDI).
The average isocyanate functionality of the polyisocyanate component A) is preferably 1.8 to 4.0, in particular 1.9 to 3.5, particularly preferably 2.0 to 3.0.
The present invention may provide that at least one polyisocyanate of the polyisocyanate component A) has been produced by gas-phase phosgenation of aliphatic, cycloaliphatic, aromatic or araliphatic polyamines. Such a process for manufacturing the polyisocyanates to be employed in accordance with the invention is described in EP 1 754 698 B1. Also employable is a process for gas-phase phosgenation as is disclosed in WO 2013/079517 A1.
The gas phase phosgenation procedure is preferably conducted such that the relevant starting substances, i.e. the polyamines upon which the polyisocyanates to be produced are based, are evaporated, optionally with addition of stabilizers and/or an inert gas, this being done at a pressure of <1000 mbar if necessary. The polyamines evaporated in this way are passed through a circuit with an average residence time of 5 to 90 minutes and a temperature of 40° C. to 190° C. and reacted with phosgene in accordance with processes of gas-phase phosgenation known per se at a temperature of 10 to 100 K above the evaporation temperature of the amines at the prevailing pressure. The above process conditions apply in particular to the manufacture of 1,3-xylylenediisocyanate and 1,4-xylylenediisocyanate. In this way, comparatively large amounts of nitrile are formed which have an advantageous effect on further processing in a composition according to the invention, in particular in terms of the transparency of molded articles manufactured therefrom. In this case—depending on the desired content of aromatic nitriles in the composition—active addition of aromatic nitriles may be eschewed for this embodiment.
Suitable modification reactions for producing the polyisocyanate components A) are, if desired, urethanization and/or allophanatization of araliphatic diisocyanates after addition of a molar deficiency of hydroxyl-functional coreactants, in particular low molecular weight mono- or polyhdric alcohols in the molecular weight range 32 to 300 g/mol, for example methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, secbutanol, the isomeric pentanols, hexanols, octanols and nonanols, n-decanol, ndodecanol, n-tetradecanol, n-hexadecanol, n-octadecanol, cyclohexanol, the isomeric methylcyclohexanols, hydroxymethylcyclohexane, 3-methyl-3-hydroxymethyloxetane, 1,2-ethanediol, 1,2- and 1,3-propanediol, the isomeric butanediols, pentanediols, hexanediols, heptanediols and octanediols, 1,2- and 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, 4,4′-(1-methylethylidene)biscyclohexanol, diethylene glycol, dipropylene glycol, 1,2,3-propanetriol, 1,1,1-trimethylolethane, 1,2,6-hexanetriol, 1,1,1-trimethylolpropane, 2,2-bis(hydroxymethyl)-1,3-propanediol or 1,3,5-tris(2-hydroxyethyl)isocyanurate, or any desired mixtures of such alcohols. Preferred alcohols for producing urethane- and/or allophanate-modified polyisocyanate components A) are the mentioned monoalcohols and diols having 2 to 8 carbon atoms.
Specific descriptions of urethane- and/or allophanate-modified polyisocyanates based on araliphatic diisocyanates may be found in EP-A 1 437 371, EP-A 1 443 067, JP-A 2005161611691, JP-A 2005162271 for example.
If one or more polyisocyanates manufactured via gas-phase phosgenation are to be employed for the composition according to the invention, a preferred configuration of the composition according to the invention specifies that the polyisocyanate component contains at least 30 wt % based on the polyisocyanate component of polyisocyanate produced by gas-phase phosgenation, in particular at least 50 wt %, more preferably at least 80 wt % or even at least 90 wt %, particularly preferably at least 95 wt % or even at least 96 or at least 98 wt %.
When polyisocyanate manufactured by gas-phase phosgenation is employed it is preferable for least one nitrile present as a byproduct in the polyisocyanate component present by gas-phase phosgenation to form a further constituent of the polyisocyanate component. In addition to the polyisocyanate manufactured by gas-phase phosgenation the polyisocyanate component may quite possibly also have had a polyisocyanate manufactured by a different production route added to it, for example a polyisocyanate produced by liquid-phase phosgenation.
Depending on the nitrile content of the polyisocyanate component the proportion of polyisocyanates produced by routes other than gas-phase phosgenation may be for example up to 19 wt % based on the polyisocyanate component A), or else up to 14 wt %, up to 9 wt %, up to 4 wt % or up to 3 wt %.
In a preferred embodiment of the composition according to the invention in which at least one polyisocyanate manufactured by gas-phase phosgenation is employed the polyisocyanate component contains at least 0.005 wt % based on the polyisocyanate component A) of at least one aromatic nitrile, in particular at least 0.01 wt %, preferably 0.005 to 15 wt %, more preferably 0.01 to 5 wt %, particularly preferably 0.1 to 2 wt % or even 0.1 to 1 wt %.
As already stated hereinabove the polyisocyanate components employed in accordance with the invention and manufactured by gas-phase phosgenation may already contain a certain proportion of nitriles as a result of the production process which may be influenced inter alia by the nature of the polyamines employed in the reaction and moreover by the choice of the reaction conditions, in particular the pressure and the reaction temperature. This applies in particular for the polyisocyanates particularly preferred in the context of the present invention 1,3-bis(isocyanatomethyl)benzene (1,3-XDI) and 1,4-bis(isocyanatomethyl)benzene (1,4-XDI) which after the gas-phase phosgenation generally exhibit comparatively high contents of corresponding nitriles.
Independently of the presence of one or more polyisocyanates produced by gas-phase phosgenation the composition preferably contains 0.0025 to 10 wt % based on the total composition of aromatic nitrile, in particular 0.005 to 5 wt %, more preferably 0.01 to 3 wt % and particularly preferably 0.05 to 2 wt %. These usage quantities of aromatic nitriles—regardless of whether they are present as a byproduct of the gas phase phosgenation or are entirely or partly actively added—are particularly advantageous because this makes it possible to produce optical molded articles that are particularly transparent and free from cloudiness from polythiourethanes, for example lenses.
In the context of the present invention the content of nitriles is determined by derivatization with diethylamine and subsequent HPLC-MS by integration of the areas of the signals in the UV range. The HPLC-MS measurement may be performed with the following program for example:
Synapt G2-S HR-MS, ACQUITY UPLC (Waters) QS. No.: 02634
UV: PDA (Total Absorbance Chromatogram)
Column: Kinetex 100×2.1 mm_1.7 μm
Column temperature: 30° C.
The mobile phase consisted of:
Solvent: A) water+0.05% formic acid
B) acetonitrile+0.05% formic acid
Flow rate: 0.5 ml/min
Gradient: t0/5% B_t0.5/5% B_t6/100% B_t7/100% B_t7.1/5% B_t8/5% B
In the context of the present invention it is preferable when the nitrile is derived from the same polyamine as the polyisocyanate. This applies both for the nitriles present as a result of the production process and for any subsequently added nitriles. This is particularly advantageous since the identical basic chemical structure to that of the polyisocyanate manufactured during the gas-phase phosgenation ensures that a particularly good promotion effect is achieved by the nitrile.
It is moreover particularly preferable for the nitrile to contain at least one further functional group which is in particular a group that can be incorporated into the polythiourethane network to prevent later migration of the nitrile out of the molded article and may particularly preferably be an isocyanate group. This shall be elucidated hereinbelow with reference to the example 1,3-bis(isocyanatomethyl)benzene (1,3-XDI). This diisocyanate may be manufactured by gas-phase phosgenation of 1,3-bis(aminomethyl)benzene. The particularly preferred isocyanatonitrile in this case is 3-(isocyantomethyl)benzonitrile.
The reaction of such an isocyanatonitrile with the thiol component can form nitrile-modified thiourethanes. This is shown using the example of 3-(isocyantomethyl)benzonitrile.
Here, R2 represents the radical of the polythiol employed. For 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (DMPT) the radical R2 represents the following structural unit, wherein the left-hand bond line in the formula represents the bond to the sulfur atom in the above structure.
It is also possible for both thiol groups of the DMPT to react with one molecule of 3-(isocyantomethyl)benzonitrile respectively, thus forming the structure:
Analogous compounds may also be formed with optionally employed polyols. First, in general terms, the reaction product of 3-(isocyantomethyl)benzonitrile with a polyol where R1 represents the radical of the polyol employed:
A nitrile-modified urethane is thus formed. When a diol is employed it is also possible for both OH groups to react with one molecule of 3-(isocyantomethyl)benzonitrile respectively, thus forming the structure:
In the context of the present invention the term aromatic nitriles is to be understood as meaning compounds having a nitrile group bonded directly to an aromatic and preferably having a molar mass of <1000 g/mol, particularly preferably <500 g/mol.
In a preferred configuration of the composition according to the invention the nitrile is selected from benzonitrile, 3-(isocyanatomethyl)benzonitrile, 4-(isocyanatomethyl)benzonitrile, 3-(chloromethyl)benzonitrile, 4-(chloromethyl)benzonitrile, 3-cyanobenzoic acid, 4-cyanobenzoic acid, 2-hydroxybenzonitrile, 3-hydroxybenzonitrile, 4-hydroxybenzonitrile, 3-cyanobenzoyl chloride, 4-cyanobenzoyl chloride or mixtures thereof, in particular benzonitrile, 3-(chloromethyl)benzonitrile, 4-(chloromethyl)benzonitrile, 3-(isocyanatomethyl)benzonitrile, and/or 4-(isocyanatomethyl)benzonitrile, particularly preferably 3-(isocyanatomethyl)benzonitrile, and/or 4-(isocyanatomethyl)benzonitrile. The use of these nitriles is advantageous particularly when a polyisocyanate component which has relatively large proportions of 1,3-XDI and/or 1,4-XDI, such as >50 wt % based on the polyisocyanate component A), or which in terms of the polyisocyanates consists completely of these compounds, is used. In these cases a particularly pronounced improvement in the optical properties of a polythiourethane article manufactured therefrom may be observed, especially as regards transparency thereof.
In a particularly preferred embodiment of the composition according to the invention the polyisocyanate is selected from 1,3-bis(isocyanatomethyl)benzene (1,3-XDI) and the nitrile from 3-(isocyanatomethyl)benzonitrile and/or that the polyisocyanate is selected from 1,4-bis(isocyanatomethyl)benzene (1,4-XDI) and the nitrile from 4-(isocyanatomethyl)benzonitrile.
The composition according to the invention further contains a thiol component B). Said component contains or consists of at least one polythiol having a functionality of thiol groups of at least two per molecule, in particular from 2 to 6, preferably from 2 to 4, particularly preferably from 3 to 4. It is also possible to employ mixtures of polythiols of different functionality and odd-numbered average functionalities may therefore arise. In the context of the present invention the term polythiol is to be understood as meaning organic thiols having two or more thiol groups. The syllable “poly” accordingly relates essentially to the number of thiol groups per molecule and, as stated above for the polyisocyanate compounds, does not necessarily mean that the polythiol must have an oligomeric, much less a polymeric, structure. Notwithstanding, the polythiols used according to the invention may quite possibly also have a polyether basic structure, a polythioether basic structure or a mixed basic structure composed of O-ether and S-ether units.
The polythiol may have an average molecular weight of 80 (methanedithiol) to about 12000 g/mol, preferably 250 to 8000 g/mol.
Suitable polythiols include for example methanedithiol, 1,2-ethanedithiol, 1,1-propanedithiol, 1,2-propanedithiol, 1,3-propanedithiol, 2,2-propanedithiol, 1,4-butanedithiol, 2,3-butanedithiol, 1,5-pentanedithiol, 1,6-hexanedithiol, 1,2,3-propanetrithiol, 1,1-cyclohexanedithiol, 1,2-cyclohexanedithiol, 2,2-dimethylpropane-1,3-dithiol, 3,4-dimethoxybutane-1,2-dithiol and 2-methylcyclohexane-2,3-dithiol, polythiols containing thioether groups, for example 2,4-dimercaptomethyl-1,5-dimercapto-3-thiapentane, 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane, 4,8-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 4,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 4,5-bis(mercaptoethylthio)-1,10-dimercapto-3,8-dithiadecane, tetrakis(mercaptoethyl)methyl)methane, 1,1,3,3-tetrakis(mercaptomethylthio)propane, 1,1,5,5-tetrakis(mercaptomethylthio)-3-thiapentane, 1,1,6,6-tetrakis(mercaptomethylthio)-3,4-dithiahexane, 2-mercaptoethylthio-1,3-dimercaptopropane, 2,3-bis(mercaptoethylthio)-1-mercaptopropane, 2,2-bis(mercaptomethyl)-1,3-dimercaptopropane, bis(mercaptomethyl) sulfide, bis(mercaptomethyl) disulfide, bis(mercaptoethyl) sulfide, bis(mercaptoethyl) disulfide, bis(mercaptopropyl) sulfide, bis(mercaptoproropyl) disulfide, bis-(mercaptomethylthio)methane, tris(mercaptomethylthio)methane, bis(mercaptoethylthio)methane, tris(mercaptoethylthio)methane, bis(mercaptopropylthio)methane, 1,2-bis(mercaptomethylthio)ethane, 1,2-bis(mercaptoethylthio)ethane, 2-(mercaptoethltthio)ethane, 1,3-bis(mercaptomethylthio)propane, 1,3-bis(mercaptopropylthio)propane, 1,2,3-tris(mercaptomethylthio)propane, 1,2,3-tris(mercaptoethylthio)propane, 1,2,3-tris(mercaptopropylthio)propane, tetrakis(mercaptomethylthio)methane, tetrakis(mercaptoethylthiomethyl)methane, tetrakis(mercaptopropylthiomethyl)methane, 2,5-dimercapto-1,4-dithiane, 2,5-bis(mercaptomethyl)-1,4-dithiane and oligomers thereof obtainable as described in JP-A 07118263, 1,5-bis(mercaptopropyl)-1,4-dithiane, 1,5-bis(2-mercaptoethylthiomethyl)-1,4-dithiane, 2-mercaptomethyl-6-mercapto-1,4-dithiacycloheptane, 2,4,6-trimercapto-1,3,5-trithiane, 2,4,6-trimercaptomethyl-1,3,5-trithiane and 2-(3-bis(mercaptomethyl)-2-thiapropyl)-1,3-dithiolane, polyester thiols, for example ethylene glycol bis(2-mercaptoacetate), ethylene glycol bis(3-mercaptopropionate), diethylene glycol 2-mercaptoacetate, diethylene glycol 3-mercaptopropionate, 2,3-dimercapto-1-propanol 3-mercaptopropionate, 3-mercapto-1,2-propanediol bis(2-mercaptoacetate), 3-mercapto-1,2-propanediol bis(3-mercaptopropionate), trimethylolpropane tris(2-mercaptoacetate), trimethylolpropane tris(3-mercaptopropionate), trimethylolethane tris(2-mercaptoacetate), trimethylolethane tris(3-mercaptopropionate), pentaerythritol tetrakis(2-mercaptoacetate), pentaerythritol tetrakis(3-mercaptopropionate), glycerol tris(2-mercaptoacetate), glycerol tris(3-mercaptopropionate), 1,4-cyclohexanediol bis(2-mercaptoacetate), 1,4-cyclohexanediol bis(3-mercaptopropionate), hydroxymethyl sulfide bis(2-mercaptoacetate), hydroxymethyl sulfide bis(3-mercaptopropionate), hydroxyethyl sulfide 2-mercaptoacetate, hydroxyethyl sulfide 3-mercaptopropionate, hydroxymethyl disulfide 2-mercaptoacetate, hydroxymethyl disulfide 3-mercaptopropionate, 2-mercaptoethyl ester thioglycolate and bis(2-mercaptoethyl ester) thiodipropionate and also aromatic thio compounds, for example 1,2-dimercaptobenzene, 1,3-dimercaptobenzene, 1,4-dimercaptobenzene, 1,2-bis(mercaptomethyl)benzene, 1,4-bis(mercaptomethyl)benzene, 1,2-bis(mercaptoethyl)benzene, 1,4-bis(mercaptoethyl)benzene, 1,2,3-trimercaptobenzene, 1,2,4-trimercaptobenzene, 1,3,5-trimercaptobenzene, 1,2,3-tris(mercaptomethyl)benzene, 1,2,4-tris(mercaptomethyl)benzene, 1,3,5-tris(mercaptomethyl)benzene, 1,2,3-tris(mercaptoethyl)benzene, 1,3,5-tris(mercaptoethyl)benzene, 1,2,4-tris(mercaptoethyl)benzene, 2,5-toluenedithiol, 3,4-toluenedithiol, 1,4-naphthalenedithiol, 1,5-naphthalenedithiol, 2,6-naphthalenedithiol, 2,7-naphthalenedithiol, 1,2,3,4-tetramercaptobenzene, 1,2,3,5-tetramercaptobenzene, 1,2,4,5-tetramercaptobenzene, 1,2,3,4-tetrakis(mercaptomethyl)benzene, 1,2,3,5-tetrakis(mercaptomethyl)benzene, 1,2,4,5-tetrakis(mercaptomethyl)benzene, 1,2,3,4-tetrakis(mercaptoethyl)benzene, 1,2,3,5-tetrakis(mercaptoethyl)benzene, 1,2,4,5-tetrakis(mercaptoethyl)benzene, 2,2′-dimercaptobiphenyl and 4,4′-dimercaptobiphenyl.
It is preferable when the polythiol is selected from 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane, 2,5-bismercaptomethyl-1,4-dithiane, 1,1,3,3-tetrakis(mercaptomethylthio)propane, 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 4,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 4,8-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, trimethylolpropane tris(3-mercaptopropionate), trimethylolethane tris(2-mercaptoacetate), pentaerythritol tetrakis(2-mercaptoacetate) and/or pentaerythritol tetrakis(3-mercaptopropionate).
Aside from the thiol component B) the composition according to the invention may also contain other components typically reacted with polyisocyanates. These are in particular the customary polyetherpolyols, polyesterpolyols, polyetherpolyesterpolyols, polythioetherpolyols, polymer-modified polyetherpolyols, graft polyetherpolyols, in particular those based on styrene and/or acrylonitrile, polyetherpolyamines, hydroxyl-containing polyacetals and/or hydroxyl-containing aliphatic polycarbonates known from polyurethane chemistry which typically have a weight-average molecular weight of 106 to 12 000 g/mol, preferably 250 to 8000 g/mol. A broad overview of suitable coreactants B) may be found for example in N. Adam et al.: “Polyurethanes”, Ulhnann's Encyclopedia of Industrial Chemistry, Electronic Release, 7th ed., chap. 3.2-3.4, Wiley-VCH, Weinheim 2005.
In the context of the present invention the term polythiourethane is to be understood as meaning a polymer where more than half to all of the bonds between the polyisocyanate and the isocyanate-reactive component(s) are thiourethane groups. Thus, other bonds may be present in a proportion of less than half, for example urethane or urea bridges. In this case the composition according to the invention also contains other isocyanate-reactive component(s). These merely optional components are more particularly described hereinbelow.
Suitable polyetherpolyols, if used, are for example those of the type referred to in DE-A 2 622 951, column 6, line 65-column 7, line 47, or EP-A 0 978 523, page 4, line 45 to page 5, line 14, provided that they conform to the above indications relating to functionality and molecular weight. Particularly preferred polyetherpolyols B) are addition products of ethylene oxide and/or propylene oxide onto glycerol, trimethylolpropane, ethylenediamine and/or pentaerythritol.
Suitable polyesterpolyols, if used, are for example those of the type referred to in EP-A 0 978 523, page 5, lines 17 to 47, or EP-A 0 659 792, page 6, lines 8 to 19, provided that they conform to the above indications, preferably those having a hydroxyl number of 20 to 650 mg KOH/g.
Suitable polyacetalpolyols, if used, are for example the known reaction products of simple glycols, for example diethylene glycol, triethylene glycol, 4,4′-dioxyethoxydiphenyldimethylmethane (adduct of 2 mol of ethylene oxide onto bisphenol A) or hexanediol, with formaldehyde, or else polyacetals produced by polycondensation of cyclic acetals, for example trioxane.
Aminopolyethers or mixtures of aminopolyethers may likewise be suitable, i.e. polyethers having isocyanate-reactive groups which are composed of primary and/or secondary, aromatic or aliphatic amino groups to an extent of at least 50 equivalent %, preferably at least 80 equivalent %, and of primary and/or secondary, aliphatic hydroxyl groups as the remainder. Suitable aminopolyethers of this type are for example the compounds referred to in EP-A 0 081 701, column 4, line 26 to column 5, line 40. Likewise suitable as starting component E) are amino-functional polyetherurethanes or -ureas such as are producible for example by the process of DE-A 2 948 419 by hydrolysis of isocyanate-functional polyether prepolymers or else amino-containing polyesters of the abovementioned molecular weight range.
Further suitable isocyanate-reactive components are, for example, also those described in EP-A 0 689 556 and EP-A 0 937 110, for example special polyols obtainable by reaction of epoxidized fatty acid esters with aliphatic or aromatic polyols to bring about epoxide ring opening.
Hydroxyl-containing polybutadienes too may optionally be employed.
Sulfur-containing hydroxyl compounds are moreover also suitable as isocyanate-reactive components. Examples that may be mentioned here are mercaptoalcohols, for example 2-mercaptoethanol, 3-mercaptopropanol, 1,3-dimercapto-2-propanol, 2,3-dimercaptopropanol and dithioerythritol, thioether-containing alcohols, for example di(2-hydroxyethyl)sulfide, 1,2-bis(2-hydroxyethylmercapto)ethane, bis(2-hydroxyethyl)disulfide and 1,4-dithiane-2,5-diol, or sulfur-containing diols having a polyesterurethane-, polythioesterurethane-, polyesterthiourethane- or Polythioesterthiourethane structure of the type referred to in EP-A 1 640 394.
The compositions according to the invention may also contain as isocyanate-reactive compounds low molecular weight, hydroxyl- and/or amino-functional components, i.e. those in a molecular weight range from 60 to 500 g/mol, preferably from 62 to 400 g/mol.
These are for example simple mono- or polyhydric alcohols having 2 to 14, preferably 4 to 10 carbon atoms, for example 1,2-ethanediol, 1,2- and 1,3-propanediol, the isomeric butanediols, pentanediols, hexanediols, heptanediols and octanediols, 1,10-decanediol, 1,2- and 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, 4,4′-(1-methylethylidene)biscyclohexanol, 1,2,3-propanetriol, 1,1,1-trimethylolethane, 1,2,6-hexanetriol, 1,1,1-trimethylolpropane, 2,2-bis(hydroxymethyl)-1,3-propanediol, bis(2-hydroxyethyl)hydroquinone, 1,2,4- and 1,3,5-trihydroxycyclohexane or 1,3,5-tris(2-hydroxyethyl)isocyanurate.
Examples of suitable low molecular weight amino-functional compounds are aliphatic and cycloaliphatic amines and aminoalcohols having primary and/or secondary amino groups, for example cyclohexylamine, 2-methyl-1,5-pentanediamine, diethanolamine, monoethanolamine, propylamine, butylamine, dibutylamine, hexylamine, monoisopropanolamine, diisopropanolamine, ethylenediamine, 1,3-diaminopropane, 1,4-diaminobutane, isophoronediamine, diethylenetriamine, ethanolamine, aminoethylethanolamine, diaminocyclohexane, hexamethylenediamine, methyliminobispropylarmine, iminobispropylamine, bis(aminopropyl)piperazine, aminoethylpiperazine, 1,2-diaminocyclohexane, triethylenetetramine, tetraethylenepentamine, 1,8-p-diaminomenthane, bis(4-aminocyclohexyl)methane, bis(4-amino-3-methylcyclohexyl)methane, bis(4-amino-3,5-dimethylcyclohexyl)methane, bis(4-amino-2,3,5-trimethylcyclohexyl)methane, 1,1-bis(4-aminocyclohexyl)propane, 2,2-bis(4-aminocyclohexyl)propane, 1,1-bis(4-aminocyclohexyl)ethane, 1,1-bis(4-aminocyclohexyl)butane, 2,2-bis(4-aminocyclohexyl)butane, 1,1-bis(4-amino-3-methylcyclohexyl)ethane, 2,2-bis(4-amino-3-methylcyclohexyl)propane, 1,1-bis(4-amino-3,5-dimethylcyclohexyl)ethane, 2,2-bis(4-amino-3,5-dimethylcyclohexyl)propane, 2,2-bis(4-amino-3,5-dimethylcyclohexyl)butane, 2,4-diaminodicyclohexylmethane, 4-aminocyclohexyl-4-amino-3-methylcyclohexylmethane, 4-amino-3,5-dimethylcyclohexyl-4-amino-3-methylcyclohexylmethane and 2-(4-aminocyclohexyl)-2-(4-amino-3-methylcyclohexyl)methane.
Examples of aromatic polyamines, in particular diamines, having molecular weights below 500 which are suitable isocyanate-reactive compounds B) are for example 1,2- and 1,4-diaminobenzene, 2,4- and 2,6-diaminotoluene, 2,4′- and/or 4,4′-diaminodiphenylmethane, 1,5-diaminonaphthalene, 4,4′,4″-triaminotriphenylmethane, 4,4′-bis(methylamino)diphenylmethane or 1-methyl-2-methylamino-4-aminobenzene, 1-methyl-3,5-diethyl-2,4-diaminobenzene, 1-methyl-3,5-diethyl-2,6-diaminobenzene, 1,3,5-trimethyl-2,4-diaminobenzene, 1,3,5-triethyl-2,4-diaminobenzene, 3,5,3′,5′-tetraethyl-4,4′-diaminodiphenylmethane, 3,5,3′,5′-tetraisopropyl-4,4′-diaminodiphenylmethane, 3,5-diethyl-3′,5′-diisopropyl-4,4′-diaminodiphenylmethane, 3,3′-diethyl-5,5′-diisopropyl-4,4′-diaminodiphenylmethane, 1-methyl-2,6-diamino-3-isopropylbenzene, liquid mixtures of polyphenylpolymethylenepolyamines, such as are obtainable in known fashion by condensation of aniline with formaldehyde, and any desired mixtures of such polyamines. In this connection particular mention may be made of mixtures of 1-methyl-3,5-diethyl-2,4-diaminobenzene with 1-methyl-3,5-diethyl-2,6-diaminobenzene in a weight ratio of 50:50 to 85:15, preferably of 65:35 to 80:20.
The use of low molecular weight amino-functional polyethers having molecular weights below 500 g/mol is likewise possible. These are for example those which have primary and/or secondary, aromatic or aliphatic amino groups, said amino groups optionally being bonded to the polyether chains via urethane or ester groups, and which are obtainable by known processes already described above in connection with production of the higher molecular weight aminopolyethers.
Sterically hindered aliphatic diamines having two secondary amino groups may optionally also be employed as isocyanate-reactive components, for example the reaction products of aliphatic and/or cycloaliphatic diamines with maleic or fumaric esters disclosed in EP-A 0 403 921 or the hydrogenation products of Schiff bases obtainable from aliphatic and/or cycloaliphatic diamines and ketones, for example diisopropyl ketone, described in DE-A 19 701 835 for example.
In addition to the mentioned starting components A) and B), auxiliary and additive agents (C), for example catalysts, surface-active agents, UV stabilizers, antioxidants, fragrances, mold release agents, fillers and/or pigments, may optionally be co-used.
For the purpose of reaction acceleration it is possible to employ, for example, customary catalysts known from polyurethane chemistry. By way of example mention may be made here of tertiary amines, for example triethylamine, tributylamine, dimethylbenzylamine, diethylbenzylamine, pyridine, methylpyridine, dicyclohexylmethylamine, dimethylcyclohexylamine, N,N,N′,N′-tetramethyldiaminodiethyl ether, bis(dimethylaminopropyl)urea, N-methyl-1 N-ethylmorpholine, N-cocomorpholine, N-cyclohexylmorpholine, N,N,N,N′-tetramethylethylenediamine, N,N,N′,N′-tetramethyl-1,3-butanediamine, N,N,N′,N′-tetramethyl-1,6-hexanediamine, pentamethyldiethylenetriamine, N-methylpiperidine, N-dimethylaminoethylpiperidine, N,N′-dimethylpiperazine, N-methyl-N′-dimnethylaminopiperazine, 1,8-diazabicyclo(5.4.0)undec-7-ene (DBU), 1,2-dimethylimidazole, 2-methylimidazole, N,N-dimethylimidazol-phenylethylamine, 1,4-diazabicyclo-(2,2,2)-octane, bis(N,N-dimethylaminoethyl)adipate; alkanolamine compounds, for example triethanolamine, triisopropanolamine, N-methyl- and N-ethyldiethanolamine, dimethylaminoethanol, 2-(N,N-dimethylaminoethoxy)ethanol, N,N′,N″-tris(dialkylaminoalkyl)hexahydrotriazines, for example N,N′,N″-tris(dimethylaminopropyl)-s-hexahydrotriazine and/or bis(dimethylaminoethyl) ether; metal salts, for example inorganic and/or organic compounds of iron, lead, bismuth, zinc and/or tin in customary oxidation states of the metal, for example iron(II) chloride, iron(III) chloride, bismuth(II) bismuth(III) 2-ethylhexanoate, bismuth(III) octoate, bismuth(III) neodecanoate, zinc chloride, zinc 2-ethylcaproate, tin(II) octoate, tin(II) ethylcaproate, tin(II) palmitate, dibutyltin(IV) dilaurate (DBTL), dibutyltin(IV) dichloride, dimethyltin(IV) dichloride or lead octoate; amidines, for example 2,3-dimethyl-3,4,5,6-tetrahydropyrimidine; tetraalkylammonium hydroxides, for example tetramethylammonium hydroxide; alkali metal hydroxides, for example sodium hydroxide, and alkali metal alkoxides, for example sodium methoxide and potassium isopropoxide, and also alkali metal salts of long-chain fatty acids having 10 to 20 carbon atoms and optionally lateral OH groups.
Preferred catalysts C) for use are tertiary amines, bismuth and tin compounds of the type mentioned.
The catalysts mentioned by way of example may be used in the production of the lightfast polyurethane, polythiourethane and/or polyurea masses according to the invention individually or in the form of any desired mixtures with one another and are optionally employed in amounts of 0.001 to 5.0 wt %, preferably 0.002 to 2 wt %, calculated as the total amount of catalysts employed based on the total amount of the starting compounds employed.
The compositions according to the invention are preferably used to produce transparent, compact moldings having a high refractive index.
The articles obtained from the compositions according to the invention feature very good light resistance even as such, i.e. without addition of appropriate stabilizers. Nevertheless, known UV-protectants (light stabilizers) or antioxidants may be co-used as auxiliary and additive agents C).
Suitable UV stabilizers C) are for example piperidine derivatives, for example 4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 4-benzoyloxy-1,2,2,6,6-pentamethylpiperidine, bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, methyl (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, bis(2,2,6,6-tetramethyl-4-piperidyl) suberate or bis(2,2,6,6-tetramethyl-4-piperidyl) dodecanedioate, benzophenone derivatives, for example 2,4-dihydroxy-, 2-hydroxy-4-methoxy-, 2-hydroxy-4-octoxy-, 2-hydroxy-4-dodecyloxy- or 2,2′-dihydroxy-4-dodecyloxybenzophenone, benzotriazole derivatives, for example 2-(5-methyl-2-hydroxyphenyl)benzotriazole, 2-(5-tert-butyl-2-hydroxyphenyl)benzotriazole, 2-(5-tert-octyl-2-hydroxyphenyl)benzotriazole, 2-(5-dodecyl-2-hydroxyphenyl)benzotriazole, 2-(3,5-di-tert-butyl-2-hydroxyphenyl)-5-chlorobenzotriazole, 2-(3,5-di-tert-amyl-2-hydroxyphenyl)benzotriazole, 2-(3,5-di-tert-butyl-2-hydroxyphenyl)benzotriazole, 2-(3-tert-butyl-5-methyl-2-hydroxyphenyl)-5-chlorobenzotriazole and esterification products of 2-(3-tert-butyl-5-propionato-2-hydroxyphenyl)benzotriazole with polyethylene glycol 300, oxalanilides, for example 2-ethyl-2′-ethoxy- or 4-methyl-4′-methoxyoxalanilide, salicylic esters, for example phenyl salicylate, 4-tert-butylphenyl salicylate and 4-tert-octylphenyl salicylate; cinnamic ester derivatives, for example methyl α-cyano-β-methyl-4-methoxycinnamate, butyl α-cyano-methyl-4-methoxycinnamate, ethyl α-cyano-β-phenylcinnamate and isooctyl α-cyano-β-phenylcinnamate, or malonic ester derivatives, for example dimethyl 4-methoxybenzylidenemalonate, diethyl 4-methoxybenzylidenemalonate, and dimethyl 4-butoxybenzylidenemalonate. These light stabilizers may be employed either individually or in any desired combinations with one another.
Suitable antioxidants C) are for example the known sterically hindered phenols, for example 2,6-di-tert-butyl-4-methylphenol (lonol), pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate), octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, triethylene glycol bis(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate, 2,2′-thiobis(4-methyl-6-tert-butylphenol), 2,2′-thiodiethylbis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate), which may be employed either individually or in any desired combinations with one another.
Further auxiliary and additive agents C) for optional co-use are for example the known flame retardants, for example trischlorethyl phosphate, ammonium phosphate or polyphosphate, fillers, for example barium sulfate, diatomaceous earth, carbon black, whiting or else reinforcing glass fibers.
Finally, it is also possible to co-use the internal mold release agents, dyes, pigments, hydrolysis inhibitors, fungistatic and bacteriostatic substances known per se.
It is particularly preferable when the composition according to the invention contains as component C) at least one mold release agent selected from mono- and/or dialkyl phosphates and/or mono- and/or dialkoxyalkyl phosphates. As mono- and/or dialkyl phosphates, particularly mono- and/or dialkyl phosphates having 2 to 18 carbon atoms in the alkyl radical, preferably 8 to 12 carbon atoms, are. Particularly preferred mono/dialkoxyalkyl phosphates have 2 to 12 carbon atoms in the alkoxyalkyl radical and up to three ether groups per alkoxyalkyl radical, the abovementioned mono-/alkoxyalkyl phosphates having in particular 4 to 10 carbon atoms in the alkoxyalkyl radical. The preferred mono-/dialkyl phosphates and mono-/dialkoxyalkyl phosphates are particularly advantageous since in addition to their actual function as a mold release agent they also have a favorable effect on the reaction rate in the reaction of the polyisocyanate component with the thiol component in the respect that their addition reduces the reaction rate of the two components with one another. This ultimately results in molded articles of higher optical quality and in simpler handling of the composition after the mixing of the components.
Suitable mold release agents are for example methyl phosphate, dimethyl phosphate, methoxyethyl phosphate, methoxypropyl phosphate, di(methoxyethyl) phosphate, methoxyethyl ethoxyethyl phosphate, methoxyethyl propoxyethyl phosphate, di(methoxypropyl) phosphate, ethyl phosphate, diethyl phosphate, ethoxyethyl phosphate, di(ethoxyethyl) phosphate, ethoxypropyl phosphate, ethoxyethyl propoxyethyl phosphate, di(ethoxypropyl) phosphate, ethoxyethyl butoxyethyl phosphate, isopropyl phosphate, diisopropyl phosphate, propoxyethyl phosphate, di(propoxyethyl) phosphate, propoxypropyl phosphate, di(propoxylpropyl) phosphate, butyl phosphate, dibutyl phosphate, butoxyethyl phosphate, butoxypropyl phosphate, di(butoxyethyl) phosphate, pentoxyethyl phosphate, bis(2-ethylhexyl) phosphate, di(hexyloxyethyl) phosphate, octyl phosphate, dioctyl phosphate, decyl phosphate, isodecyl phosphate, diisodecyl phosphate, isodecyloxyethyl phosphate, di(decyloxyethyl) phosphate, dodecyl phosphate, didoceyl phosphate, tridecanol phosphate, bis(tridecanol) phosphate, stearyl phosphate, distearyl phosphate and any desired mixtures of such compounds.
The compositions according to the invention advantageously contain 0.01 to 4 wt % of mono-/dialkylphosphates and/or mono-/dialkylalkoxyphosphates, preferably 0.02 to 2 wt %, based on the overall composition. The abovementioned usage amounts relate to the total content of these substances as mold release agents.
A particularly preferable composition according to the invention for producing transparent polythiourethane articles contains or consists of
The present invention further provides a process for producing transparent polythiourethane articles by reaction of a composition containing or consisting of
The preferred embodiments and definitions set out above apply analogously to the compositions employed in the process according to the invention.
The process may in particular be performed without solvent addition, i.e. in solvent-free fashion, and the nitrile addition is not to be understood as solvent addition in this context.
Irrespective of the type of chosen starting substances in the process according to the invention the reaction of the polyisocyanate mixtures A) with the thiol component B) and optionally further isocyanate-reactive components is effected adhering to an equivalent ratio of isocyanate groups to isocyanate-reactive groups of 0.5:1 to 2.0:1, preferably of 0.7:1 to 1.3:1, more preferably of 0.8:1 to 1.2:1.
In the process according to the invention the components of the composition according to the invention are preferably mixed, optionally in solvent-free form, in the abovestated equivalent ratio of isocyanate groups to isocyanate-reactive groups using suitable mixing apparatuses and charged into open or closed molds by any desired method, for example by simple hand-pouring but preferably using suitable machines, for example the low-pressure or high-pressure machines customary in polyurethane technology, or by the RIM process. Curing may be performed in a temperature range of 40° C. to 180° C., preferably of 50° C. to 140° C., particularly preferably of 60° C. to 120° C., and optionally under elevated pressure of up to 300 bar, preferably up to 100 bar, particularly preferably up to 40 bar.
The polyisocyanates and optionally also the other starting components may be degassed by application of vacuum.
The molded articles thus produced from the according to the invention can generally be demolded after a short time, for example after 2 to 60 min. A post-curing at a temperature of 50° C. to 100° C., preferably at 60° C. to 90° C., may optionally follow.
Compact light- and weather-resistant polythiourethane articles having high resistance toward solvents and chemicals and outstanding mechanical properties, in particular an excellent heat resistance even at higher temperatures of for example 80° C., are obtained in this way. Compared to the prior art systems which do not contain aromatic nitriles the molded articles according to the invention feature a lower propensity for formation of cloudiness.
The present invention further provides a compact transparent polythiourethane article obtainable by reaction of the components of the composition according to the invention. This polythiourethane article may be a glass-replacement part, an optical, optoelectronic or electronic component part, an optical lens or a spectacle glass. Specific applications are for example production of/use as glass-replacement panes, for example sunroofs, front, rear or side panes in automotive or aeronautical production, as safety glass, solar modules, light emitting diodes, lenses or collimators, as are employed for example as auxiliary optics in LED lamps or automotive headlamps.
However, a particularly preferred field of application for the molded polythiourethane articles according to the invention obtainable from the compositions according to the invention is the production of lightweight plastic spectacle glasses having a high refractive index and a high Abbe number. Spectacle glasses produced according to the invention feature outstanding mechanical properties, in particular hardness and impact resistance and also good scratch resistance and are moreover easy to process and colorable as desired.
The present invention further relates to the use of aromatic nitriles for producing transparent polythiourethane articles.
The present invention further provides a mixture of a polyisocyanate having a functionality of isocyanate groups of at least 2 per molecule and at least one aromatic nitrile for producing compact transparent polythiourethane articles.
The invention will now be more particularly discussed with reference to exemplary embodiments.
All percentages are based on weight, unless stated otherwise.
The NCO contents were determined by titrimetry as per DIN EN ISO 11909.
Measurement of the refractive indices and Abbe numbers was effected using a Zeiss Model B Abbe refractometer as per DIN EN ISO 489:1999-08.
Transmission and haze measurements as per ASTM D 1003 were performed with a Byk Haze-Gard Plus using standard light type D65 (defined in DIN 6173).
The chemicals used were employed without further pretreatment:
Tinuvin® 571: alkylphenol-substituted benzotriazole (BASF)
Zelec UN: mixture of long-chain mono- and dialkyl phosphate (Steppan)
DBC: dibutyltin dichloride (Acros Organics)
DMPT: 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (Bruno Bock GmbH)
Desmodur W: H12-MDI, NCO functionality 2 (Bayer MaterialScience AG)
Benzonitrile (Merck KGaA)
Performing the gas-phase phosgenation of 1,3-XDA
In a plant for gas-phase phosgenation comprising an amine evaporation stage as per
After an average residence time in the reactor of 0.48 seconds the gas stream containing the reaction product 1,3-XDI was cooled by injection cooling with monochlorobenzene and condensed, the temperature of the liquid phase in the quench being about 90° C. The content of 3-chloromethylbenzyl isocyanate determined by gas chromatography was 0.4% based on the sum of 1,3-XDI and 3-CI-XI. The reaction mixture was then freed of HCl and phosgene and worked up by distillation. The yield of 1,3-XDI was 95% of theory.
In the above described plant 160 kg/h of 1,3-XDA were analogously evaporated at a pressure of 500 mbar abs. with introduction of a nitrogen stream of 4 kg/h, the temperature in the pumped circulation circuit (3200 kg/h) being kept at 150° C. by cooling in a heat exchanger (WT). 500 ppm Tinuvin © 571 had previously been added to the pumped circulation circuit. The supply temperature to the evaporator (V) was 240° C., the entry temperature of the cooling medium into the heat exchanger (WT) was 40° C. and the average residence time of the 1,3-XDA in the pumped circulation circuit was 43 minutes. The stream composed of gaseous 1,3-XDA and nitrogen was heated to 280° C. in a further heat exchanger and supplied to the reactor via the coaxial nozzle. Simultaneously and in parallel thereto, 500 kg/h of phosgene were heated to 310° C. and on the annular space left free by the nozzle likewise continuously supplied to the reactor in which the two reactant streams were mixed and brought to reaction. The velocity of the gas stream in the reactor was about 20 m/s and the velocity ratio of the amine stream to the phosgene stream was 8.8. After an average residence time in the reactor of 0.46 seconds the gas stream containing the reaction product 1,3-XDI was cooled by injection cooling with monochlorobenzene and condensed, the temperature of the liquid phase in the quench being about 90° C.
The content of 3-chloromethylbenzyl isocyanate determined by gas chromatography was 0.3% based on the sum of 1,3-XDI and 1.3-CI-XI. The reaction mixture was then freed of HCl and phosgene and worked up by distillation. The yield of 1,3-XDI was 92% of theory.
Production of 1,3-XDI manufactured by liquid-phase phosgenation
With stirring and cooling a solution of 5 parts by weight of 1,3-XDA in 50 parts by weight of monochlorobenzene was metered into a solution of 20 parts by weight of phosgene in 25 parts by weight of monochlorobenzene at 0-10° C. and on completion of the addition the mixture was allowed to reach room temperature. The temperature was subsequently increased to reflux with introduction of phosgene according to gas evolution and phosgenation was continued until the solution eventually became clear. Once the clear point had been reached (about 4-5 h) phosgenation was continued for a further 30 minutes. Phosgene introduction was then terminated and the mixture was refluxed with introduction of nitrogen until phosgene was no longer detectable in the offgas.
The reaction mixture was then worked up by distillation to obtain XDI as a colorless liquid having a boiling point of 130° C./0.2 mbar. The yield of 1,3-XDI was 80% of theory
2 kg of the XDI obtained in example 2 were fractionally distilled through a column. The first 500 g were discarded as forerun and 1 kg of colorless 1,3-XDI was obtained as the main fraction. This fraction was admixed with 1.4 g of Zelec UN (Steppan) at room temperature and left to stand for 24 h. The HC content of the sample after distillation, measured as per ASTM specification D4663-98, was 105 ppm. The content of 3-isocyanatomethylbenzonitrile was determined by dissolving 1 g of 1,3-XDI in 100 ml of acetonitrile. 100 μl of this solution were mixed with 900 μl of a diethylamine solution (0.2 g of diethylamine in 100 ml of acetonitrile) and stored at 65° C. for 30 minutes prior to HPLC-MS measurement. Purity was determined by integration of the areas of the signals in the UV spectrometer. It was assumed that all compounds show the same UV absorption and that no compounds without a UV absorption are present in the samples. A further assumption was that no degradation reactions take place during measurement. The following program was chosen for HPLC-MS measurement:
Synapt G2-S HR-MS, ACQUITY UPLC (Waters) QS. No.: 02634
UV: PDA (Total Absorbance Chromatogram)
Column: Kinetex 100×2.1 mm_1.7 μm
Column temperature: 30° C.
The mobile phase consisted of:
Solvent: A) water+0.05% formic acid
B) acetonitrile+0.05% formic acid
Flow rate: 0.5 ml/min
Gradient: t0/5% B_t0.5/5% B_t6/100% B_t7/100% B_t7.1/5% B_t8/5% B
The sample was found to contain 98.4% 1,3-XDI and 0.7% 3-isocyanatomethylbenzonitrile.
2 kg of the XDI obtained in example 3 were fractionally distilled through a column. The first 800 g were discarded as forerun and 700 g of colorless 1,3-XD1 were obtained as the main fraction. This fraction was admixed with 0.98 g of Zelec UN at room temperature and left to stand for 24 h. The HC content of the sample after distillation, measured as per ASTM specification D4663-98, was 108 ppm. Analogously to example 4, purity determination by HPLC was performed. No 3-isocyanatomethylbenzonitrile was found in the course of this. The proportion of 1,3-XDI was 95.4%.
Production of polythiourethane articles:
In a flask, 0.002 g of dibutyltin dichloride (DBC) were dissolved in 94.59 g of 1,3-XDI from example 4 and the mixture was evacuated at 10 mbar for 30 minutes. 90.00 g of DMPT (4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane) were then added into the flask and the final mixture was stirred and degassed at 10 mbar for 30 minutes. The mixture was then filtered through a 5 μm filter, drawn into a syringe and the casting mold was completely filled therewith. The casting mold was prepared by clamping together two glass shell molds (85 mm diameter, internal radius 88 mm, Shamir Insight, Inc., IL) with a gap of 8 mm and a plastic sealing ring to form a casting cavity. The mold gap is 8 mm at each point of the lens.
The filled casting mold was cured in a drying cabinet with the temperature profile: 15 hours at 65° C.; 2 hours at 100° C. and a further 2 hours at 120′C. The casting mold was then cooled to room temperature and, after complete cooling, first the sleeve and then the two glass articles were manually removed.
A spectacle glass blank that was completely clear, transparent and free from cloudiness was obtained in this way.
Transmission was 90.3% for standard light type D65, haze was 2.1. The refractive index nE was 1.67 at 23° C.
Analogously to example 6 a spectacle glass blank was produced using 1,3-XDI from example 5. This spectacle glass blank was completely cloudy, transmission was only 29.7%, haze was 100.
In a flask, 94.59 g of 1,3-XDI from example 5 were admixed with 9.25 g of benzonitrile, 0.002 g of dibutyltin dichloride (DBC) were dissolved therein and the mixture was evacuated at 10 mbar for 30 minutes. 90.00 g of DMPT (4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane) were then added into the flask and the final mixture was stirred and degassed at 10 mbar for 30 minutes. The mixture was then subsequently subjected to further processing as in example 6 to afford a spectacle glass blank.
A spectacle glass blank that was completely clear, transparent and free from cloudiness was obtained in this way.
Transmission was 86.3% for standard light type D65, haze was 2.9. The refractive index nE was 1.67 at 23° C.
In a flask, 0.011 g of dibutyltin dichloride (DBC) were dissolved in 131.00 g of Desmodur W, 10.89 g of benzonitrile and 1.31 g of Zelec UN and the mixture was evacuated at 10 mbar for 30 minutes. 85.50 g of DMPT (4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane) were then added into the flask and the final mixture was stirred and degassed at 10 mbar for 30 minutes. 20 g of the mixture were then added to a closable PP beaker (75 g ointment pot, internal diameter 50 mm) and cured in a drying cabinet with the temperature profile: 8 hours at 65° C.; 2 hours at 100° C. and a further 6 hours at 120° C. The casting mold was then cooled to room temperature and, after complete cooling, the casting was demolded. The casting was free from cloudiness and transparent.
In a flask, 0.22 g of dibutyltin dichloride (DBC) were dissolved in 131.00 g of Desmodur W and 2.6 g of Zelec UN and the mixture was evacuated at 10 mbar for 30 minutes. 85.50 g of DMPT (4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane) were then added into the flask and the final mixture was stirred and degassed at 10 mbar for 30 minutes. 20 g of the mixture were then added to a closable PP beaker (75 g ointment pot, internal diameter 50 mm) and cured in a drying cabinet with the temperature profile: 8 hours at 65° C.; 2 hours at 100° C. and a further 6 hours at 120° C. The casting mold was then cooled to room temperature and, after complete cooling, the casting was demolded. The casting was milky-white.
| Number | Date | Country | Kind |
|---|---|---|---|
| 14164345.2 | Apr 2014 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2015/057960 | 4/13/2015 | WO | 00 |
