Patent Application
20170320887
The present invention refers to a novel urethane acrylate being a reaction product of at least a diol component, a component having acrylic unsaturation and an isocyanate component, wherein said diol component comprises at least one alkoxylated 2,4,8,10-tetraoxaspiro[5.5]-undecane-3,9-dialkanol.
Radiation, such as UV-curing coatings for industrial applications has been rising constantly for many years. Less productive and/or less environmentally friendly systems have gradually been replaced by radiation technology, and an ever increasing number of new applications is being found for radiation curing coatings. Radiation curable polyurethane acrylates have been well known for more than two decades. The most common are coatings based on urethane acrylate or methacrylate oligomers, which represent a major class of coatings widely used in industry. Such coatings are used for protection purposes as well as applications such as heat and/or radiation curing coatings, inks and adhesives. Cured coatings typically yield films with for instance a good combination of toughness and elasticity. The urethane acrylate is the main part of the composition, thus determining the properties of both the liquid and the cured product.
There is, however, despite the large amount of commercially available urethane acrylates and derivatives thereof, due to for instance environmental concerns and legislation and/or new application areas, a substantial and ever growing demand for novel, safer, more efficient and/or more versatile urethane acrylates. A major search, for safer urethane acrylates, is directed to suitable replacements for presently used urethane acrylates based on bisphenols and alkoxylated bisphenols, such as the frequently used ethoxylated bisphenol A. Bisphenols and derivatives thereof are known to be endocrine disrupters that mimic for instance oestrogen and are associated with irritation to the respiratory system, risks of serious damage to the eyes and neural system, risk of sensitisation by skin contact and risk of impaired fertility. The hazardous effects of inadvertent exposure to bisphenols and bisphenol releasing chemicals in professionals and in the general population should thus be avoided.
Hydrogenated bisphenols have been suggested as replacement for corresponding bisphenols. There are, however, significant drawbacks associated with the use of for instance hydrogenated bisphenol A. Drawbacks include for instance the fact that hydrogenated bisphenol A is a high melting solid and thus difficult to handle in a plant environment and the fact that reactions between liquids and high melting solids are difficult to moderate. It would accordingly be desirable to have a diol which provide the property advantages of a high melting point diol with reduced processing problems. A further disadvantage is that production of hydrogenated bisphenols means handling of and contact with the hazardous bisphenols.
An object of the present invention is to provide a novel urethane acrylate having at least one acrylic, methacrylic and/or methylacrylic double bond. A further object is to provide a suitable replacement for urethane acrylates involving handling of hazardous and/or restricted compounds such as bisphenols, bisphenol releasing substances and especially compounds derived from bisphenols, such as alkoxylated bisphenols.
It has now quite unexpectedly been found that an alkoxylated 2,4,8,10-tetraoxaspiro[5.5]-undecane-3,9-dialkanol is a versatile compound in most applications involving urethane acylates. The novel urethane acrylate of the present invention can thus advantageously replace urethane acrylates based on alkoxylated bisphenols, as well as bisphenols, as a product being safer to handle, safer to produce and/or being environmentally friendlier.
The novel urethane acrylate of the present invention is a reaction product of a raw material composition comprising at least (A) a diol component, (B) a component having acrylic unsaturation and (C) an isocyanate component. Said component (A) comprises at least one alkoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-dialkanol of formula
wherein each substituent R individually is a linear or branched C1-C8 alkyl group and m, n, p and q individually are integers each being at least 1, said component (B) comprises, in embodiments thereof, at least one hydroxyalkyl acrylate, hydroxyalkyl methacrylate and/or hydroxyalkyl methylacrylate, whereby hydroxyalkyl preferably is hydroxy-C1-C12-alkyl, which can be exemplified by hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, trimethylolpropane di(meth)acrylate and pentaerythritol tri(meth)acrylate, and/or comprises acrylic acid, methacrylic acid and/or a methylacrylic acid, such as crotonic or isocrotonic acid, or a corresponding alkyl ester thereof, and wherein said component (C) comprises at least one di or polyisocyanate or a derivative thereof.
In preferred embodiments of said alkoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-dialkanol, m and p, in above formula, are independently integers each being between 1 and 6, such as between 1 and 4 and n and q are independently integers each being between 1 and 10, such as between 1 and 8, between 1 and 6 or between 1 and 4. Substituent R in above formula is in likewise preferred embodiments an alkyl group of formula
The most preferred embodiments of said alkoxylated 2,4,8,10-tetraoxaspiro[5.5]-undecane-3,9-dialkanol include alkoxylated, such as ethoxylated, propoxylated and/or butoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diethanol.
The especially preferred embodiments of said alkoxylated 2,4,8,10-tetraoxaspiro[5.5]-undecane-3,9-diethanol (pentaerythritol spiroglycol) is an ethoxylated and/or propoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diethanol having 1-10, such as 1-6, 1-5, 1-4, 1-3, 1-2 or most preferably 3-6 ethoxy and/or propoxy units/hydroxyl group.
Said component (A) comprises, in preferred embodiments of the novel urethane acrylate according to the present invention, 50-100%, such as 70-100% or 80-100%, by weight of said alkoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-dialkanol, such as said ethoxylated, propoxylated and/or butoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diethanol, optionally in combination with one or more other hydroxyfunctional compound(s) known in the art. In likewise preferred embodiments, said component (B) comprises 50-100% by weight of said at least one hydroxyalkyl acrylate, hydroxyalkyl methacrylate and/or hydroxyalkyl methylacrylate and/or 50-100% by weight of said acrylic acid, methacrylic acid and/or a methylacrylic acid and/or an alkyl ester thereof.
Said di or polyisocyanate is preferably and advantageously selected from the group consisting of toluene diisocyanate, diphenyl methane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, tetramethylxylene diisocyanate, dicyclohexyl methane diisocyanate, furan diisocyanate, tetrahydrofuran diisocyanate, cyclohexylene diisocyanate, xylene diisocyanate, naphthalene diisocyanate, phenylene diisocyanate, nonane triisocyanate and/or triphenyl methane triisocyanate.
Said raw material composition may, in addition to said components (A), (B) and (C), comprise one or more carboxylic acids, such as octanoic acid, 2-ethylhexanoic acid, 2-propylheptanoic acid, cecanoic acid and/or trimethylhexanoic acid.
Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilise the present invention to its fullest extent. The following preferred specific embodiments are, therefore, to be construed as merely illustrative and not limitative.
In the following Examples 1 and 2 illustrate an embodiment of the present invention and Examples 1 and 3 a comparative product based on bisphenol A ethoxylate. Example 4 refer to curing of the products yielded in Examples 2 and 3. Table 1 returns properties measured on products yielded in Examples 2 and 3.
An adduct between isophorone diisocyanate and hydroxyethyl acrylate was produced for use in productions of urethane acrylates as disclosed in Examples 2 and 3 (comparative).
175.0 parts by weight of isophorone diisocyanate and 0.6 parts by weight of methoxy phenol, as inhibitor, were charged to a reaction vessel, equipped with a heating device, temperature control, stirrer, air inlet and a cooler. 86.8 parts by weight of hydroxyethyl acrylate was successively during 10 minutes charged and 0.03 part by weight of dibutyltinlaurate as catalyst was subsequently charged to the reaction mixture. The temperature was now slowly raised to 60-70° C. and the reaction was allowed to continue until the theoretical remaining NCO value was reached. Yielded reaction product was finally cooled to room temperature.
54.5 parts by weight of an ethoxylated 2,4,8,10-tetraoxaspiro[5.5]undecane-3,9-diethanol, having an average of 4-5 ethylene oxide units/hydroxyl group (pentacrythritol spiroglycol ethoxylate, Perstorp Specialty Chemicals AB), 0.2 parts by weight of methoxy phenol as inhibitor and 133.0 parts by weight of toluene as azeotropic solvent were charged to a reaction vessel, equipped with a heating device, temperature control, stirrer, air inlet and reflux. 100.0 parts by weight of the adduct yielded in Example 1 was now slowly charged to the reaction mixture followed by charging of 0.03 parts by weight of dibutyltinlaurate as catalyst. The temperature was rapidly raised to 65° C. and maintained until the NCO value was close to 0. Toluene was now evaporated and remaining reaction product was cooled to room temperature. Properties measured on obtained product are given in Table 1.
Example 2 was repeated with the difference that 52.4 parts by weight of a bisphenol A ethoxylate having an average of 4 ethoxy units/phenolic hydroxyl group (Sigma Aldrich Co) was charged instead of 54.5 parts by weight of the ethoxylated 2,4,8,10-tetraoxaspiro-[5.5]undecane-3,9-diethanol. Properties measured on obtained product are given in Table 1.
The products yielded in Examples 2 and 3 (comparative) were, after addition of 1.0 part by weight of Irgacure 500 (Photoinitiator, Ciba Specialty Chemicals Inc.), coated on glass and steel panels at a dry film thickness of 40 μm and cured.
The coated panels were first placed in an oven for 30 minutes at 50° C., cooled to room temperature and subsequently UV cured. UV curing was performed by means of a UV-lamp of 80 W/cm2 and at a belt speed of 20 m/min. The lacquers were allowed to pass the UV-lamp 4 times. The samples were after curing conditioned for 24 hours at 23±2° C. and 50±5% relative humidity followed by measuring of film hardness, flexibility and gloss.
Recorded Results:
| Number | Date | Country | Kind |
|---|---|---|---|
| 1300292-8 | Apr 2013 | SE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/SE2014/000024 | 3/11/2014 | WO | 00 |
