Radiation-curable urethane acrylates containing iso-cyanate...

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Compositions to be polymerized by wave energy wherein said...

Reexamination Certificate

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C522S092000, C522S093000, C522S096000, C522S097000, C522S107000, C522S139000, C522S140000, C522S173000, C522S174000, C522S167000

Reexamination Certificate

active

06599955

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field Of The Invention
The invention relates to radiation-curable urethane acrylates containing isocyanate groups and their use as coating compositions with a particularly good adhesion to the coated substrate.
2. Description Of The Prior Art
Coating compositions which can be cured by high-energy radiation have an advantage over thermosetting coating compositions because of the lower energy consumption for the curing and their higher rate of curing. Radiation-curable coating compositions can furthermore be applied without a solvent, any co-used reactive thinners which may be necessary being simultaneously co-polymerized. However, a disadvantage of radiation-curable coating compositions, in particular those based on ethylenically unsaturated acrylates, is the high volume shrinkage during curing. Due to this shrinkage, adhesion to the substrate, e.g. to metals (steel sheets, copper etc.) and certain types of wood, is often inadequate.
It was already known from DE-A 3,616,434 that radiation-curable binders cure to coatings which adhere well on difficult types of wood if the substrate has been coated beforehand with a primer of compounds containing isocyanate groups (adhesive base). The obvious disadvantage of this process, however, is an additional lacquering step for application of the primer. The known process of admixing a low amount of lacquer polyisocyanates to the binder has the disadvantage that after radiation curing the lacquer polyisocyanates remain free. These polyisocyanates then are bonded neither to the substrate nor the film and therefore are able to adversely influence the hardness of the film or leave the film. US-A 5,234,970 claims a composition comprising
a) a compound containing isocyanate groups and ethylenically unsaturated groups,
b) reactive (meth)acrylate thinners and
c) if appropriate photoinitiators.
The disadvantage of this composition is that the reactive thinners b) contain OH groups, so that the stability of the composition in storage is limited even without any contact with atmospheric humidity.
One object of the present invention is therefore to provide coating compositions which can be cured by radiation and do not have the disadvantages mentioned for the prior art.
It has been found that certain urethane acrylates which contain free isocyanate groups can be cured by UV radiation on the substrates which are difficult to coat, such as certain woods, plastics and metals, to give coatings which adhere well.
These coating compositions contain almost no hydroxyl groups, so that they display high stability in storage in sealed vessels.
SUMMARY OF THE INVENTION
The invention relates to radiation-curable coating composition containing:
a) 10 to 100 wt. % of a urethane (meth)acrylate which contains both (meth)-acryloyl groups and free isocyanate groups,
b) 0 to 90 wt. % of (meth)acrylates which contain (meth)acryloyl groups but no free isocyanate groups or any isocyanate-reactive groups, the wt. % under a) and b) adding up to 100 wt. %, based on the weight of a)+b), and
c) 0 to 10 wt. %, based on the sum of components a) and b) of a UV initiator for free radical polymerization.
The invention also relates to metal, plastic, film, wood, leather and mineral substrates coated with the above-mentioned radiation-curable coating composition.
DETAILED DESCRIPTION OF THE INVENTION
Compounds a) are prepared from monohydric alcohols containing (meth)acryloyl groups and di- or polyisocyanates. Preparation processes for urethane (meth)acrylates are known and are described e.g. in DE-A 1,644,798, DE-A 2,115,373 or DE-A 2,737,406. For the urethane (meth)acrylates according to the invention containing free isocyanate groups, the equivalent ratio of NCO groups to OH groups is 1:0.2 to 1:0.8, preferably 1:0.3 to 1:0.6.
Monohydric alcohols containing (meth)acryloyl groups are understood as including both esters, containing a free hydroxyl group, of acrylic acid or methacrylic acid with dihydric alcohols, such as 2-hydroxyethyl, 2- or 3-hydroxypropyl or 2-, 3- or 4-hydroxybutyl (meth)acrylate, and mixtures of such compounds. Monohydric alcohols containing (meth)acryloyl groups or reaction products substantially containing such alcohols, which are obtained by esterification of n-hydric alcohols with (meth)acrylic acid, are also possible. It is also possible to employ mixtures of different alcohols, so that n represents an integer or a fractional number from 2 to 4, preferably 3(n-0.8) to (n-1.2), preferably (n-1) mol of (meth)acrylic acid is employed per mol of the alcohols mentioned. These compounds or product mixtures include the reaction products of i) glycerol, trimethylolpropane and/or pentaerythritol, low molecular weight alkoxylation products of such alcohols (such as ethoxylated or propoxylated trimethylolpropane, for example the addition product of ethylene oxide on trimethylolpropane of OH number 550), or of mixtures of such at least trihydric alcohols with dihydric alcohols (such as ethylene glycol or propylene glycol), with ii) (meth)acrylic acid in the molar ratio mentioned.
These compounds have a number-average molecular weight Mn of 116 to 1,000, preferably 116 to 750, and more preferably 116 to 158.
Suitable di- or polyisocyanates include aromatic, araliphatic, cycloaliphatic, and aliphatic compounds, aliphatic compounds being preferred. Examples include butylene-diisocyanate, hexamethylene-diisocyanate (HDI), isophorone-diisocyanate (IPDI), trimethylhexamethylene-diisocyanate (2,2,4- and/or 2,4,4-trimethylhexa-methylene-diisocyanate), neopentyl diisocyanate, dicyclohexylmethane-diisocyanate or 4-isocyanatomethyl-1,8-octane-diisocyanate and derivatives of these diisocyanates containing with a urethane, isocyanurate, allophanate, biuret, uretdione and/or iminooxadiazinedione groups. Di- or polyiso-cyanates which contain urethane groups and are based on di- or polyisocyanates and dihydric alcohols are also suitable.
The curing (addition reaction) can be accelerated in a known manner by means of suitable catalysts, such as, tin octoate, dibutyltin dilaurate or tertiary amines.
To increase the stability of the coating compositions according to the invention (e.g. towards premature polymerization and storage), 0.01 to 0.3 wt. %, based on the total weight of the reactants, of polymerization inhibitors or known antioxidants can be added to the reaction mixture. Suitable such additives are described e.g. in “Methoden der organischen Chemie” (Houben-Weyl), 4th edition, volume XIV/1, p. 433 et seq., Georg Thieme Verlag, Stuttgart 1961. Examples which may be mentioned include phenols, cresols and/or hydroquinones and quinones.
In a preferred variant, an oxygen-containing gas, preferably air, is passed through the reaction mixture during the preparation in order to prevent undesirable poly-merization of the (meth)acrylates.
The components mentioned under b) are (meth)acrylates which contain (meth)-acryloyl groups but no free isocyanate groups nor any isocyanate-reactive groups. Such binders are described, for example, in P.K.T. Oldring (ed.), Chemistry & Technology of UV & EB Formulations for Coatings, Inks & Paints, vol. 2, 1991, SITA Technology, London p. 31-235. Examples which may be mentioned include urethane acrylates, certain polyester acrylates and certain polyether acrylates.
The binders according to the invention can also be employed in a form diluted by solvents. Examples of suitable solvents include acetone, 2-butanone, ethyl acetate, n-butyl acetate, methoxypropyl acetate or low molecular weight esters of (meth)acrylic acid. Such mono-, di- or oligoesters of (meth)acrylic acid are known compounds in coating technology and are called reactive thinners and, as compounds which polymerize in during curing, lower the viscosity of the non-cured coating. Such compounds are described in P.K.T. Oldring (ed.), Chemistry & Technology of UV & EB Formulations for Coatings, Inks & Paints, vol. 2, 1991, SITA Technology, London p. 237-235. Examples include the esters of acrylic acid or methacrylic acid, preferably acrylic acid, with mono-,

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