GB1590412A - Creation of Inventions and Patents with Artificial Intelligence

GB1590412A – Radiation curable compositions
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GB1590412A – Radiation curable compositions
– Google Patents
Radiation curable compositions

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Publication number
GB1590412A

GB1590412A
GB3081477A
GB3081477A
GB1590412A
GB 1590412 A
GB1590412 A
GB 1590412A
GB 3081477 A
GB3081477 A
GB 3081477A
GB 3081477 A
GB3081477 A
GB 3081477A
GB 1590412 A
GB1590412 A
GB 1590412A
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GB
United Kingdom
Prior art keywords
isocyanate
unsaturated
monomeric
polyol
adipic acid
Prior art date
1976-08-02
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

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GB3081477A
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Lord Corp

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Lord Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1976-08-02
Filing date
1977-07-22
Publication date
1981-06-03

1976-08-02
Priority claimed from US05/710,776
external-priority
patent/US4112017A/en

1977-07-22
Application filed by Lord Corp
filed
Critical
Lord Corp

1981-06-03
Publication of GB1590412A
publication
Critical
patent/GB1590412A/en

Status
Expired
legal-status
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Current

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Classifications

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS

C08G18/00—Polymeric products of isocyanates or isothiocyanates

C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen

C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen

C08G18/40—High-molecular-weight compounds

C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain

C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups

C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups

C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS

C08G18/00—Polymeric products of isocyanates or isothiocyanates

C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen

C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen

C08G18/67—Unsaturated compounds having active hydrogen

C08G18/671—Unsaturated compounds having only one group containing active hydrogen

Description

(54) RADIATION CURABLE COMPOSITIONS
(71) We, LORD CORPORATION, a corporation of the State of Pennsylvania, United
States of America, located at 1635 West 12th Street, Erie, State of Pennsylvania, United
States of America, do hereby declare the invention for which we pray that a Patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:
This invention relates to unsaturated addition-polymerizable urethane resins and to radiation curable compositions containing such resins.
Increasing concern with energy, environmental protection, and health factors have cooperated to enhance the potential of radiation curable coatings. In principle, such coatings comprise a polymerizable mixture that can be applied as a thin film to a substrate and polymerized at a rapid rate by exposure to a radiation source such as an electron beam, plasma arc, and ultra violet light. Advantages of radiation curable coatings include a practical method of at least reducing air pollution from volatile vapor loss, rapid cure rates at ambient temperatures, reduced operating costs, the use of heat-sensitive substrates, and improved product performance.
Among the more notable achievements in the field of radiation curing has been the development of the so-called 100 percent reactive solids systems based on unsaturated addition-polymerizable urethane resin. A characteristic feature of such systems is the substantial absence of conventional inert volatile solvents. Instead, the systems contain reactive diluents which react during curing to become an integral part of the cured coating. Such systems have been widely accepted commercially. While such systems provide highperformance coatings which can be cured at high line speeds, they have also provided a new set of problems for the coatings formulators.
While unsaturated addition-polymerizable urethane resins can be prepared by several known reaction routes, the preferred method of preparation for obtaining premium-quality coatings is by capping an isocyanate-functional prepolymer with an appropriate additionpolymerizable monomer having a single isocyante-reactive active hydrogen group, with the reaction being effected in the presence of a diluent system which is inert with respect to the capping reaction but which is reactive with the unsaturated addition-polymerizable urethane resins at cure conditions. Among the more vexing of the problems associated with radiation curable compositions containing such polymerizable urethane resins, regardless of how the resin is prepared, are the high viscosity of the resin compositions which makes the application by conventional industrial techniques extremely difficult, if not impossible; the difficulty of solvating the resinous compounds; physical instability of the compositions which is evidenced by thixotropy and/or cloudiness leading to eventual separation of the compositions into distinct resin-rich and monomer-rich phases; and an incompatability between resinous and non-resinous components which is more evident with higher molecular weight components.
Because the use of conventional inert solvents/ diluents such as are employed with moisturecure polyurethanes is undesirable, there have been developed the so-called reactive diluents, which generally comprise a mixture of monofunctional and polyfunctional unsaturated addition-polymerizable monomeric compounds which are copolymerizable with the unsaturated addition-polymerizable urethane resins and thus become part of the cured coating.
However, these reactive diluents are not without problems. For example, certain of the lower molecular weight monomeric diluents are quite effective in affording clear coating compositions which can be applied by conventional industrial techniques; however, their use in diluents is often undesirable because of their relatively high volatility, even at the relatively low temperatures encountered during the curing cycle, which results in diluent loss, noxious fumes, increased atmospheric emissions, and a fogging above the work surface which inteferes with energy transmission and adversely affects rate and degree of cure. These problems which are associated with the higher solvating low molecular weight monomer diluents can be largely overcome by employing as reactive monomer diluents acrylic and methacrylic acid esters containing at least six carbon atoms in the non-acid moiety of the molecule. While such acrylic and methyacrylic acid esters are preferred because they do not present the volatility, noxious and curing problems associated with the lower molecular weight diluents, they are not without their problems. Generally, greater amounts of the acrylic and methacrylic acid esters having at least six carbon atoms in the non-acid mdiety of the molecule are required for effective viscosity reduction. Because of their lower solvating power, the problems of physical instability and incompatibility of resin and diluent components are generally greater with diluents containing the less-volatile acrylic and methacrylic acid esters. Thus there remains a need to produce radiation curable compositions which will remain homogenous, which can be readily and uniformly applied to substrates and which can be rapidly and fully cured to a dried film having the desired physical and chemical properties. It is equally important that harmful emissions to the atmosphere, noxiousness and other hazards be at least reduced, if not entirely eliminated.
During the course of extensive studies relating to the physical and chemical nature of radiation curable compositions containing unsaturated addition-polymerizable urethane resins, it was discovered that the composition of the resinous component markedly affects viscosity and physical stability of the compositions, as well as solubility and compatibility of the resinous components with respect to the reactive diluents. More particularly, in accordance with the present invention, it has been discovered that unsaturated additionpolymerizable urethane resins having as characteristic features reduced viscosity, improved physical stability, and which are more readily soluble in or solvatable by and compatible with organic a solvent/diluents can be obtained by employing as precursors at least one organic isocyanate compound having at least two isocyanate groups, from 30 to 100 mol percent of at least one polymeric polyol having at least two hydroxyl groups, from 70 to zero mol percent of at least one monomeric polyol having at least two hydroxyl groups, and at least one unsaturated addition-polymerizable monomeric organic compound characterized by the presence of a single isocyanate-reactive active hydrogen-containing group; provided that the amount of isocyanate compound is sufficient to afford an NCO:OH ratio, with respect to the polyol compound, of at least 2.1:1, preferably 2.3-4:1; and the average hydroxyl functionality of the polyol component is at least 2.1, preferably is in the range from 2.2 to 3.0, and most advantageously is in the range from about 2.3 to about 2.7. For brevity, unsaturated addition-polymerizable urethane resins will be referred to hereinafter in the disclosure and claims as unsaturated urethane resins. Radiation curable compositions containing the unsaturated urethane resins of the invention have an increased flowability and a substantially improved physical stability, can be readily and uniformly applied to metallic, fabric and plastic substrates by conventional industrial techniques, and rapidly cure upon exposure to a source of radiation to afford dried films having excellent properties. Unsaturated urethane resins prepared in accordance with this invention are readily solvated by and more compatible with acrylic and methacrylic acid esters having at least six carbon atoms in the non-acid moiety of the ester molecule, and permit the use of such low-volatility diluents at higher diluent levels than heretofore. The present invention further provides compositions having a more manageable viscosity at higher resin content that heretofore possible.
More particularly, In accordance with one aspect of the present invention, there is provided an unsaturated addition-polymerizable urethane resin having at least one ethylenically unsaturated group having the structure C = C and comprising the reaction product of
i) at least one organic isocyanate compound having at least two isocyanate groups;
ii) from 30 to 100 mol percent of at least one polymeric polyol having at least two hydroxyl groups; iii) from 70 to zero mol percent of at least one monomeric polyol having at least two hydroxy groups; and
iv) at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group; wherein: – said isocyanate compound is present in an amount sufficient to provide an NCO:OH ratio of at least 2.1:1, with respect to the polymeric and monomeric polyols;
said mol percents are based on total mols of the polymeric and monomeric polyols;
the average hydroxyl functionality, with respect to the polymeric and monomeric polyols, is at least 2.1, and the amount of said unsaturated addition-polymerizable organic monomeric compound having a single isocyanate-reactive active hydrogen-containing group is sufficient to provide at least one molar equivalent of active hydrogen-containing group with respect to isocyanate functionality.
In a further aspect, the invention resides in a radiation curable coating composition comprising
A. at least one unsaturated addition-polymerizable urethane resin having at least one ethylenically unsaturated group having the structureC = Cand comprising the reaction product of
i) at least one organic isocyanate compound having at least two isocyanate groups;
i) from 30 to 100 mol percent of at least one polymeric polyol having at least two hydroxyl groups;
iii) from 70 to zero mol percent of at least one monomeric polyol having at least two hydroxyl groups; and
iv) at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group; wherein:
said isocyanate compound is present in an amount sufficient to provide an NCO:OH ratio of at least 2.1:1, with respect to the polymeric and monomeric polyols;
said mol percents are based on total mols of said polymeric and monomeric polyols;
the average hydroxyl functionality, with respect to said polymeric and monomeric polyols, is at least 2. 1, and the amount of said unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group is sufficient to provide at least one molar equivalent of active hydrogen-containing group with respect to isocyanate functionality; and
B. a reactive diluent comprising at least one unsaturated addition-polymerizable monomeric organic compound which is copolymerizable with said unsaturated urethane resin;
the amount of unsaturated urethane resin being in the range from 30 to 90 weight percent, based on total weight of unsaturated urethane resin and reactive diluent.
Preferably, said isocyanate compound is present in the unsaturated urethane resin in an amount sufficient to provide an NCO:OH ratio in the range 2.3-4:1 with respect to the polymeric and monomeric polyols:
Preferably, the average hydroxyl functionality with respect to the polymeric and monomeric polyols of the unsaturated urethane resin is in the range from 2.2 to 3 and most preferably in the range 2.3 to 2.7.
Preferably, the reactive diluent of the coating composition comprises at least one unsaturated addition-polymerizable monofunctional monomeric organic compound selected from esters having the general formula
wherein R” is hydrogen or methyl and R is an aliphatic or cycloaliphatic, preferably alkyl or cycloalkyl, group having 6 to 18, preferably 6 to 9, carbon atoms.
Preferably, the coating composition contains an effective amount of at least one photoinitiator compound. The photoinitiator compound, which will generally be employed when curing is effected with a low energy radiation source such as ultraviolet light radiation, will generally be in the range from about 0.01 to about 30, preferably about 0.1 to about 15, parts by weight per 100 parts by combined weight of unsaturated urethane resin and reactive diluent.
Unsaturated urethane resins are well known in the art. Such prior art resins comprise the reaction product of at least one organic isocyanate having at least two isocyanate groups, at least one monomeric or polymeric organic compound characterized by the presence of at least two isocyanate-reactive active hydrogen-containing groups, and at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanatereactive active hydrogen-containing group, there being an excess of organic isocyanate compound with respect to said organic compounds containing at least two isocyanate reactive active hydrogen-containing groups. Unsaturated urethane resins can be prepared by several known reaction routes, with the method wherein an isocyanate-functional prepolymer, obtained by reacting an excess of organic isocyanate having at least two isocyanate groups with organic compounds having at least two active hydrogen-containing groups, is reacted with an appropriate unsaturated addition-polymerizable monomeric compound having a single isocyanate-reactive active hydrogen-containing group, such as 2-hydroxyethyl acrylate, being presently preferred. The various methods of preparing unsaturated urethane resins and prepolymer precursors are sufficiently well known as to require no further elaboration herein. The unsaturated urethane resins of this invention can be prepared by any of the known methods, which such resins prepared through the route of isocyanate-functional prepolymers being especially preferred.
Unsaturated urethane resins of this invention have as a first characteristic feature, at least one, preferably at least two, polymerizable ethylenically unsaturated group(s) having the structure C = C. The polymerizable ethylenically unsaturated moiety is preferably a terminal vinyl group having the structure CH2 = C. Especially preferred unsaturated urethane resins are the acrylyl urethane resins, i.e. unsaturated urethane resins containing a polymerizable acrylyl, methacrylyl, acrylamide, or methacrylamide moiety in the molecule, characterized by the presence of at least one, preferably at least two, terminal ethylenically unsaturated group(s) having the structure CH2 = C~ .
The unsaturated urethane resins of the invention are further characterized in that they are obtained from organic polyisocyanate and organic polyol precursor compounds, as these compounds have been previously defined, at the NCO:OH ratios and hydroxyl functionalities previously set forth. It will be appreciated by the person skilled in the art that there must be employed a finite amount of at least one monomeric or polymeric organic polyol having at least three hydroxyl groups if the requirement of a hydroxyl functionality of at least 2.1 is to be satisfied. The invention thus encompasses mixtures of polyols, including mixtures of polyols having two hydroxyl groups and polyols having at least three hydroxyl groups.
The polyisocyanates which can be employed in forming the isocyanate-functional prepolymer can be any organic isocyanate having at least two free isocyanate groups. Included within the purview of suitable polyisocyanates are aliphatic, cycloaliphatic, and aromatic polyisocyanates, as these terms are generally interpreted in the art. Thus it will be appreciated that any of the known polyisocyanates such as alkyl and alkylene polyisocyanates, cycloalkyl and cycloalkylene polyisocyanates, aryl and arylene polyisocyanates, and combinations such as alkylene, cycloalkylene and alkylene arylene polyisocyanates, can be employed in the practice of the present invention.
Suitable polyisocyanates include, wihtout limitation, tolylene-2,4-diisocyanate, 2,2,4trimethylhexamethylene-1, 6-diisocyanate, hexamethylene 1, 6-diisocyanate, diphenylmethane-4, 4′-diisocyanate, triphenylmethane-4, 4′-4″-triisocyanate, polymethylene polyphenylisocyanate, m-phenylene diisocyanate, p-phenylene diisocyanate, 2,6-tolylene diisocyanate, 1,5-naphthalene diisocyanate, naphthalene-1, 4-diisocyanate, diphenylene-4,4′-diisocyanate, 3 ,3′-bi-tolylene-4,4′-diisocyanate, 1,4-cyclohexylene dimethylene diisocyanate, xylylene-1,4-diisocyanate, xylylene-1,3-diisocyanate, cyclohexyl-1 ,4-diisocyanate, 4,4′-methylene-bis(cyclohexyl isocyanate), 3,3′-dimethyldiphenylmethane-4,4′-diisocyanate, isophorone diisocyanate, and the product obtained by reacting trimethylol propane and 2,4-tolylene diisocyanate in a molar ratio of 1:3.
Polyol compounds having at least two hydroxyl groups per molecule which are used in preparing the herein described unsaturated urethane resins comprise from about 30 to 100, preferably about 70 to 100, mol percent of at least one polymeric polyol and from about 70 to zero, preferably about 30 to zero mol percent of at least one monomeric polyol, including mixtures of such polyols. Polymeric and monomeric polyols are so well-known in the art that no need is seen to describe these materials in any detail. The polymeric polyhydroxy compounds can be dihydroxylated and polyhydroxylated polyethers and polyesters, including polyesters derived from caprolactone compounds, i.e., polycaprolactone polyols, The polyether and polyester polyols can be diols, triols, or tetrols, with polyester polyols comprising the reaction product of
i) at least one glycol selected from the group consisting of 1,3-butylene glycol and neopentyl glycol; ii adipic acid;
iii) isophthalic acid; and
iv) from about zero to about 50, preferably from about zero to about 30 mol percent of at least one aliphatic polyol having at least three hydroxyl groups, said mol percent being based on total mols of glycol and aliphatic polyol,
the amount of isophthalic acid being in the range of from about 1 to 50, preferably about 5 to 25, mol percent, based on total mols of adipic acid and isophthalic acid, being especially preferred, with such polyester polyols having an average hydroxyl functionality of at least 2.1 being most advantageous. Similarly, the monomeric polyols which can replace up to about 70 mol percent of the polymeric polyol compounds can be diols, triols, tetrols and the like include, without limitation thereto, compounds such as ethylene glycol, propylene glycol, diethylene glycol, glycerol, dipropylene glcyol, erythritol, pentaerythritol, trimethylol propane, and neopentyl glycol. Polyols employed in the practice of the invention will generally have molecular weights in the range from about 62 to 4,000, with molecular weights in the range from about 500 to 2,000 being presently preferred. The polymeric polyols and methods of preparing such compounds are well known in the art and require no further elaboration.
Unsaturated addition-polymerizable monomeric organic compounds having a single isocyanate-reactive active hydrogen-containing group which can be employed in the practice of the present invention include any of such compounds which have been previously used to introduce an unsaturated polymerizable moiety into a molecule via reaction between the active hydrogen-containing group and a reactive isocyanate moiety. Preferably, the active hydrogen-containing group is hydroxy. Illustrative of unsaturated addition-polymerizable monomeric organic compounds having a single isocyanate-reactive active hydrogen- containing group are 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, N-hydroxymethyl acrylamide, N-hydroxymethyl methacrylamide, diethylene glycol monoacrylate, diethylene glycol monomethacrylate, glycerine dimethacrylate, and trimethylol propane dimethacrylate. The amount of such compounds will be sufficient to provide at least one molar equivalent of active hydrogencontaining group with respect to the isocyanate functionality, and preferably is sufficient to afford an active hydrogen-containing group: NCO ratio, with respect to the amount of total free hydroxyl functions, of at least 1:1, with a small excess, 10 mol percent or less, being especially preferred.
As has been indicated, the herein described unsaturated urethane resins are preferably obtained by reacting at least one isocyanate-functional prepolymer with at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanatereactive active hydrogen-containing group, with unsaturated urethane resins having substantially no free isocyanate functionality being especially preferred. Suitable prepolymers can be prepared according to known methods from the above listed precursors, keeping in mind the requirements for NCO:OH ratio and average hydroxyl functionality. Such prepolymers can be prepared neat, but are preferably prepared in the presence of a diluent phase which is copolymerizable with the unsaturated urethane resin but is inert with respect to the prepolymer reaction and the subsequent reaction between the prepolymer and the unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group.
As noted, the radiation curable compositions of the present invention comprise a mixture of
i) at least one unsaturated urethane resin prepared in accordance with this invention; ii) a reactive diluent comprising at least one unsaturated addition-polymerizable monomeric compound which is copolymerizable with said unsaturated urethane resin and preferably containing at least one acrylic and/or methacrylic acid ester containing at least 6 carbon atoms in the non-acid moiety; the amount of unsaturated resin being from 30 to 90 weight per cent based on the total weight of unsaturated urethane resin and reactive diluent; and optionally
iii) an effective amount of at least one photoinitiator compound, generally within the compositional parameters previously set forth.
Reactive diluents which can be employed in the radiation curable compositions of this invention include any of such diluents which have been or are being used for this purpose.
Broadly, suitable reactive diluents comprise at least one unsaturated addition-polymerizable monomer which is copolymerizable with the unsaturated urethane resin upon exposure to radiation. The reactive diluent can be monofunctional or polyfunctional. A single polyfunctional diluent can be used, as can mixtures thereof; or a combination of one or more monofunctional reactive diluents and one or more polyfunctional reactive diluents can be used. Such combinations of mono- and polyfunctional reactive diluents are presently preferred. Generally, the reactive diluent will comprise from about 10 to about 65, preferably about 25 to about 50, weight percent, based on total weight of unsaturated urethane resin and reactive diluent, of the radiation curable compositions of the invention. Particularly preferred reactive diluents are unsaturated addition-polymerizable monofunctional monomeric compounds selected from the group consisting of esters having the general formula

Wherein R” and R are as previously defined. Representative of such preferred reactive monomeric diluents, without limitation thereto, are hexyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, octyl acrylate, nonyl acrylate, stearyl acrylate, and the corresponding methacrylates. Illustrative of other reactive monofunctional and polyfunctional monomeric diluents which can be employed are styrene, methyl methacrylate, butyl acrylate, isobutyl acrylate, 2-phenoxy acrylate, 2-monoxyethyl acrylate, 2-(N,N-diethylamino)-ethyl acrylate, the corresponding methacrylates, acrylonitrile, methyl acrylonitrile, methacrylamide, neopentyl glycol diacrylate, ethylene glycol diacrylate, hexylene glycol diacrylate, diethylene glycol diacrylate, trimethylol propane triacrylate, pentaerythritol di-, tri-, or tetra-acrylate, the corresponding methacrylates, and vinyl pyrrolidone. At the present time, it is preferred that the reactive diluent contain at least 50 weight percent of at least one acrylic and/or methacrylic acid ester having at least 6 carbon atoms in the non-acid moietv. with such acrvlic acid esters being preferred. The reactive diluent will comprise from about 10 to about 70, preferably about 25 to 50, weight percent, based on total weight of unsaturated urethane resin and reactive diluent of the radiation curable compositions of the invention. Reactive diluents are well known to those skilled in the art of radiation curing and the selection of an appropriate diluent system in any given instance is sufficiently encompassed by such knowledge as to require no further discussion here.
As previously indicated, a photoinitiator system will generally be employed when curing is effected by exposure to low energy radiation sources such as ultra violet light. Any of the known photoinitiators can be used within the concentration ranges previously set forth.
Illustrative photoinitiators, without limitation thereto, include benzophenone, benzoin, acetophenone, benzoin methyl ether, Michler’s ketone, benzoin butyl ether, xanthone, thioxanthone, propionphenone, fluorenone, carbazole, diethoxyacetophenone, the 2-, 3-, and 4-methylacetophenones and methoxyacetophenones, the 2- and 3- chloroxanthones and chlorothioxanthones, 2-acetyl-4-methylphenyl acetate, 2,2′-dimethoxy-2phenylacetophenone, benzaldehyde, fluorene, anthraquinone, triphenylamine, 3- and 4-allylacetophenone, p-diacetylbenzene, 3-chloro-2-nonylxanthone, and mixtures thereof.
The invention compositions can also include pigments, fillers, wetting agents, flatting agents, flow control agents, and other additives typically present in coating compositions. In some applications, the inclusion of minor amounts of inert solvents can be advantageous.
Such additive materials are well known to those skilled in the art and do not require further elaboration herein. Also well known are the concentrations at which such additives are used.
The radiation curable compositions of this invention are characterized by improved flowability, fluidity and physical stability. The compositions of this invention can be applied to wood, metal, fabric and plastic substrates in an economical and efficient manner using conventional industrial techniques and provide smooth, uniform films which are rapidly cured to dried films having excellent physical and chemical properties.
The improved coating compositions of this invention can be applied and cured by any of the conventional known methods. Application can be by roll coating, curtain coating, airless spray, dipping or by any other procedure. The cure can be effected by exposure to any high energy source, such as ionizing radiation, or low energy source, such as ultraviolet light radiation. The equipment utilized for curing, as well as the appropriate time for curing, and the conditions under which the curing is effected are well-known to those skilled in the art of radiation curing and do not require further elaboration herein.
The invention is illustrated in greater detail by the following Examples, but these examples are not to be construed as limiting the present invention. All parts, percentages and the like are by weight, unless otherwise indicated.
EXAMPLE I
Several unsaturated urethane resins are prepared in 2-ethylhexyl acrylate reactive monomer diluent at a resin concentration of 70 percent employing as precursor compounds polyester polyols, 4,4′-methylene-Bis-(cyclohexyl isocyanate), and 2-hydroxyethyl acrylate.
In each instance the polyester polyol is reacted with the isocyanate compound at NCO:OH ratios of 1.5: t .5:1,2:1,2.5:1,3:1 and 3.5:1 to form an isocyanate-functional prepolymer; and the prepolymer is reacted with 2-hydroxyethyl acrylate to form an ethylenically unsaturated acrylyl urethane having at least two terminal vinyl groups and substantially no free isocyanate functions. The polyester polyols have hydroxyl functionalities f(OH) of 2.0, 2.3, 2.5, 2.7 and 3.0. The resins are evaluated with respect to viscosity at 70% resin concentration, physical stability and compatibility in 2-ethylhexyl acrylate reactive monomer diluent. The results are reported in Table I, with the unsaturated urethane resin being identified in relation to the polyester polyol from which it is made.
TABLE I
Polyester Viscosity Physical Compatibi
Resin Polyol f(OH) NCO:OH CPS Stabilitya bility b
1 A 2.0 1.5 90,000 P 5
2 A 2.0 2.0 30,000 F 4
3 A 2.0 2.5 6,400 F 3
4 A 2.0 3.0 6,600 G 2
5 A 2.0 3.5 4,500 G 1
6 B 2.3 1.5 100,000 P 5
7 B 2.3 2.0 44,000 F 3
8 B 2.3 2.5 22,000 E S
9 B 2.3 3.0 10,000 E S
10 B 2.3 3.5 5,600 E S
11 B 2.5 1.5 GEL
12 B 2.5 2.0 66,000 F 3
13 B 2.5 2.5 24,500 E S
14 B 2.5 3.0 12,500 E S
15 B 2.5 3.5 10,000 E S
16 B 2.7 1.5 GEL
17 B 2.7 2.0 75,000 F 4
1
EXAMPLE To a composition containing 70 percent Resin 8 (hydroxy functionality 2.3 and NCO:OH ratio 2.5) in 2-ethylhexyl acrylate reactive monomer diluent, there is added the adduct of 2 moles 2-hydroxyethyl acrylate and 4,4′-methylene-bis (cyclohexyl isocyanate) in an amount sufficient to simulate an NCO:OH ratio of 3:1. No significant change in viscosity, physical stability of compatibility is noted, thus demonstrating that the benefits of this invention can only be attained by synthesizing the unsaturated urethane resins in accordance with the concepts of the invention.
EXAMPLE 111 Several formulations are prepared employing selected unsaturated urethane resins from
Example las follows:
Composition (parts by weight) A B C D E F
Resin 9 70 – – – – – Resin 14 – 70 – – – – Resin 19 – – 70 – –
Resin 20 – – – 70 –
Resin 25 – – – – 70
Resin 29 – – – – – 70
2-Ethylhexyl Acrylate 30 30 30 30 30 30
Benzoin Ether-type 1 1 1 1 1 1
Photoinitiator
Viscosity, CPS, Thousands 10 12.5 20 13 17 10
The compositions are coated onto aluminum substrates and cured by exposure to ultraviolet radiation (200 watts/inch mercury lamp) at a line speed of 50 feet per minute for three passes. The compositions are easily applied and cure to dried smooth, uniform films which are tough and flexible and have excellent chemical and physical properties.
EXAMPLE IV
A series of unsaturated urethane resins are prepared in 2-ethylhexyl acrylate reactive monomer diluent at a resin concentration of 70 percent employing as precursor compounds polyester polyol, 4,4′-methylene-bis (cyclohexyl isocyanate), and 2-hydroxyethyl acrylate. In each instance, the polyester polyol compound is reacted with the isocyanate compound at an NCO:OH ratio of 2.5:1 to form an isocyanate-functional prepolymer; and the prepolymer is fully capped with 2-hydroxyethyl acrylate to form an ethylenically unsaturated acrylyl urethane having at least two terminal vinyl groups and substantially no free isocyanate functions. The resins are evaluated with respect to solubility in 2-ethylhexyl acrylate-reactive monomer diluent and physical stability, including thixotropy and cloudiness, in 2-ethylhexyl acrylate reactive monomer diluent. The precursor materials and the results of the resin evaluation are reported in Table II.
TABLE 11 Resin Evaluation
2-Hydroxyethyl Acrylate
4,4′-Methylene-Bis (Cyclohexyl Isocyanate)
Polyester Polyol
1 Diethylene Glycol/Adipic Acid Insoluble
2 1 ,6-Hexanediol/Trimethylol Propane/Adipic Acid Thixotropic
3 1,3-Butylene Glycol/Trimethylol Propane/Adipic Acid Thixotropic
4 1,4-Butanediol/ Glycerine/ Adipic Acid (90)/ Insoluble
Isophthalic Acid (10)
5 1 3-Butylene Glycol/ Glycerine/ Adipic Acid (90)/ Soluble
Isophthalic Acid (10) 6 1,3-Butylene Glycol/ Glycerine/ Adipic Acid Insoluble
7 1 3-Butylene Glycol/ Glycerine/ Adipic Acid (75)/ Cloudy a
Isophthalic Acid (25)
8 1 ,3-Butylene Glycol/ Glycerine/ Adipic Acid (80) Cloudya
Isophthalic Acid (20)
9 1 ,4-Cyclohexanedimethylol/ Glycerine/ Adipic Acid (90)/ Insoluble
Isophthalic Acid (10) 10 1,3-Butylene Glycol (50)/Neopentyl Glycol (50)/ Soluble
Glycerine/Adipic Acid (90)/Isophthalic Acid (10) 11 1 ,3-Butylene Glycol (50)/I ,6-Hexanediol (50)/ Thixotropic
Glycerine/Adipic Acid (90)/Isophthalic Acid (10) 12 Neopentyl Glycol/Glycerine/Adipic Acid (90)/ Soluble
Isopthalic Acid (10) 13 Polycaprolactone Polyol Soluble b
a. When diluted to 60% resin concentration, time to form separate monomer-rich and
resin-rich phases is 730 days.
b. When diluted to 60% resin concentration, time to form separate monomer-rich and
resin-rich phases is 24 hours.
The data demonstrate the unsaturated urethane resins which are obtained from polyester polyols derived from 1 ,3-butylene glycol and/or neopentyl glycol, adipic acid, isophthalic acid, and, optionally, at least one polyol having at least three hydroxyl groups have a lower viscosity and improved physical stability. The data further demonstrate the necessity of employing both adipic acid and isophthalic acid as well as 1,3-butylene glycol and/or neopentyl glycol.
EXAMPLE V
To the unsaturated urethane resin-containing compositions from Example IV derived from polyester polyols 5, 10, 12 and 13 there is added an effective amount of benzoin ether-type photoinitiator. The compositions are coated onto aluminum panels and cured by exposure to ultraviolet radiation (200 watts/inch mercury lamp) at a line speed of 50 feet per minute for three passes. Compositions 5, 10 and 12 are less viscous than is composition 13.
Film properties of cured films from compositions 5, 10, 12 and 13 are substantially equivalent.
Attention is directed to our co-pending British Patent Application No. 30815/77 (Serial
No. 1590413)
WHAT WE CLAIM IS:
1. An unsaturated addition-polymerizable urethane resin having at least one ethylenically unsaturated group having the structure =C = C – and comprising the reaction product
of
i) froat least one organic isocyanate compound having at least two isocyanate groups; ii) from 30 to 100 mol percent of at least one polymeric polyol having at least two
hydroxyl groups;
iii) from 70 to zero mol percent of at least one monomeric polyol having at least two
hydroxyl groups; and
iv) at least one unsaturated addition-polymerizable monomeric organic compound hav
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (17)

**WARNING** start of CLMS field may overlap end of DESC **.
TABLE 11 Resin Evaluation
2-Hydroxyethyl Acrylate
4,4′-Methylene-Bis (Cyclohexyl Isocyanate)
Polyester Polyol
1 Diethylene Glycol/Adipic Acid Insoluble
2 1 ,6-Hexanediol/Trimethylol Propane/Adipic Acid Thixotropic
3 1,3-Butylene Glycol/Trimethylol Propane/Adipic Acid Thixotropic
4 1,4-Butanediol/ Glycerine/ Adipic Acid (90)/ Insoluble
Isophthalic Acid (10)
5 1 3-Butylene Glycol/ Glycerine/ Adipic Acid (90)/ Soluble
Isophthalic Acid (10) 6 1,3-Butylene Glycol/ Glycerine/ Adipic Acid Insoluble
7 1 3-Butylene Glycol/ Glycerine/ Adipic Acid (75)/ Cloudy a
Isophthalic Acid (25)
8 1 ,3-Butylene Glycol/ Glycerine/ Adipic Acid (80) Cloudya
Isophthalic Acid (20)
9 1 ,
4-Cyclohexanedimethylol/ Glycerine/ Adipic Acid (90)/ Insoluble
Isophthalic Acid (10) 10 1,3-Butylene Glycol (50)/Neopentyl Glycol (50)/ Soluble
Glycerine/Adipic Acid (90)/Isophthalic Acid (10) 11 1 ,3-Butylene Glycol (50)/I ,6-Hexanediol (50)/ Thixotropic
Glycerine/Adipic Acid (90)/Isophthalic Acid (10) 12 Neopentyl Glycol/Glycerine/Adipic Acid (90)/ Soluble
Isopthalic Acid (10) 13 Polycaprolactone Polyol Soluble b
a. When diluted to 60% resin concentration, time to form separate monomer-rich and
resin-rich phases is 730 days.
b. When diluted to 60% resin concentration, time to form separate monomer-rich and
resin-rich phases is 24 hours.
The data demonstrate the unsaturated urethane resins which are obtained from polyester polyols derived from 1 ,3-butylene glycol and/or neopentyl glycol, adipic acid, isophthalic acid, and, optionally, at least one polyol having at least three hydroxyl groups have a lower viscosity and improved physical stability. The data further demonstrate the necessity of employing both adipic acid and isophthalic acid as well as 1,3-butylene glycol and/or neopentyl glycol.
EXAMPLE V
To the unsaturated urethane resin-containing compositions from Example IV derived from polyester polyols 5, 10, 12 and 13 there is added an effective amount of benzoin ether-type photoinitiator. The compositions are coated onto aluminum panels and cured by exposure to ultraviolet radiation (200 watts/inch mercury lamp) at a line speed of 50 feet per minute for three passes. Compositions 5, 10 and 12 are less viscous than is composition 13.
Film properties of cured films from compositions 5, 10, 12 and 13 are substantially equivalent.
Attention is directed to our co-pending British Patent Application No. 30815/77 (Serial
No. 1590413)
WHAT WE CLAIM IS:
1. An unsaturated addition-polymerizable urethane resin having at least one ethylenically unsaturated group having the structure =C = C – and comprising the reaction product
of
i) froat least one organic isocyanate compound having at least two isocyanate groups; ii) from 30 to 100 mol percent of at least one polymeric polyol having at least two
hydroxyl groups;
iii) from 70 to zero mol percent of at least one monomeric polyol having at least two
hydroxyl groups; and
iv) at least one unsaturated addition-polymerizable monomeric organic compound hav
ing a single isocyanate-reactive active hydrogen-containing group; wherein:
said isocyanate compound is present in an amount sufficient to provide an NCO:OH ratio of at least 2.1:1, with respect to the polymeric and monomeric polyols;
said mol percents are based on total mols of the polymeric and monomeric polyols;
the average hydroxyl functionality, with respect to the polymeric and monomeric polyols, is at least 2.1, and the amount of said unsaturated addition-polymerizable organic monomeric compound having a single isocyanate-reactive active hydrogen-containing group is sufficient to provide at least one molar equivalent of active hydrogen-containing group with respect to isocyanate functionality.

2. A resin as claimed in Claim 1 and comprising the reaction product of
i) at least one isocyanate-functional prepolymer, said prepolymer comprising the reaction product of
a) said at least one organic isocyanate compound having at least two isocyanate groups;
b) from 30 to 100 mol percent of said at least one polymeric polyol having at least two
hydroxyl groups;
c) from 70 to zero mol percent of said at least one monomeric polyol having at least two
hydroxyl groups; and
ii) said at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group.

3. A resin as claimed in Claim 1 or Claim 2, wherein said NCO:OH ratio is in the range of 2.3-4:1 and said hydroxyl functionality is in the range from 2.3 to 2.7.

4. A resin as claimed in any preceding Claim, wherein said ethylenically unsaturated group is a terminal vinyl group having the structure CH2 = C.

5. A resin as claimed in any preceding Claim, wherein said polymeric polyol comprises the reaction product of
i) at least one glycol selected from 1 ,3-butylene glycol and neopentyl glycol; ii) adipic acid;
iii isophthalic acid; and
iv) from zero to 50 mol percent of at least one aliphatic polyol having at least three hydroxyl groups, said mol percent being based on total mols of said glycol and said aliphatic polyol;
the amount of isophthalic acid being present in the range from 1 to 50 mol percent, based on total mols of adipic acid and isophthalic acid.

6. A resin as claimed in Claim 5, wherein the amount of isophthalic acid is in the range from 5 to 25 mol percent.

7. An unsaturated addition-polymerizable urethane resin as claimed in Claim 1, substantially as hereinbefore described.

8. A radiation-curable coating composition comprising
A. at least one unsaturated addition-polymerizable urethane resin having at least one ethylenically unsaturated group having the structure C = C and comprising the reaction product of
i) at least one organic isocyanate compound having at least two isocyanate groups; ii) from 30 to 100 mol percent of at least one polymeric polyol having at least two hydroxyl groups;
iii) from 70 to zero mol percent of at least one monomeric polyol having at least two hydroxyl groups; and
iv) at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group; wherein:
said isocyanate compound is present in an amount sufficient to provide an NCO:OH ratio of at least 2.1: 1, with respect to the polymeric and monomeric polyols;
said mol percents are based on total mols of said polymeric and monomeric polyols;
the average hydroxyl functionality, with respect to said polymeric and monomeric polyols, is at least 2.1,and the amount of said unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group is sufficient to provide at least one molar eauivalent of active hydrogen-containing group with respect to isocyanate functionality; and
B. a reactive diluent comprising at least one unsaturated addition-polymerizable monomeric organic compound which is copolymerizable with said unsaturated urethane resin;
the amount of unsaturated urethane resin being in the range from 30 to 90 weight percent, based on total weight of unsaturated urethane resin and reactive diluent.

9. A coating composition as claimed in Claim 8, wherein said diluent contains at least one unsaturated addition-polymerizable monofunctional monomeric organic compound selected from esters having the general formula
wherein R” is hydrogen or methyl and R is an aliphatic or cycloaliphatic group having from 6 to 18 carbon atoms.

10. A coating composition as claimed in Claim 8 or Claim 9, wherein said unsaturated urethane resin comprises the reaction product of
i) at least one isocyanate-functional prepolymer, said prepolymer comprising the reaction product of
a) said at least one organic isocyanate compound having at least two isocyanate groups;
b) from 30 to 100 mol percent of said at least one polymeric polyol having at least two hydroxyl groups;
c) from 70 to zero mol percent of said at least one monomeric polyol having at least two hydroxyl groups; and
ii) said at least one unsaturated addition-polymerizable monomeric organic compound having a single isocyanate-reactive active hydrogen-containing group.

11. A coating composition as claimed in any one of Claims 8 to 10 wherein said polymeric polyol comprises the reaction product of i at least one glycol selected from 1 ,3-butylene glycol and neopentyl glycol; ii adipic acid; isophthalic acid; and
iv) from zero to 50 mol percent of at least one aliphatic polyol having at least three hydroxyl groups, said mol percent being based on total mols of said glycol and said aliphatic polyol;
the amount of isophthalic acid being present in the range from 1 to 50 mol percent, based on total mols of adipic acid and isophthalic acid.

12. A coating composition as claimed in Claim 11, wherein the amount of isophthalic acid is in the range from 5 to 25 mol percent.

13. A coating composition as claimed in any one of Claims 8 to 12, wherein said
NCO:OH ratio is in the range of 2.3:1 to about 4:1 and said hydroxyl functionality is in the range from 2.3 to 2.7.

14. A coating composition as claimed in any one of Claims 8 to 13, and containing an effective amount of at least one photoinitiator compound.

15. A radiation curable coating composition as claimed in Claim 8 substantially as hereinbefore described with reference to the Examples.

16. A method of coating a substrate comprising applying to the substrate a coating composition as claimed in Claim 14
and exposing the coated substrate to ultraviolet radiation for a time sufficient to cure the coating.

17. A substrate coated by a method as claimed in Claim 16

GB3081477A
1976-08-02
1977-07-22
Radiation curable compositions

Expired

GB1590412A
(en)

Applications Claiming Priority (2)

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Priority Date
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US71077576A

1976-08-02
1976-08-02

US05/710,776

US4112017A
(en)

1976-07-23
1976-08-02
Radiation curable coating compositions

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true

GB1590412A
(en)

1981-06-03

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ID=27108521
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Expired

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(en)

1976-08-02
1977-07-22
Radiation curable compositions

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JPS5317694A
(en)

AU
(1)

AU516173B2
(en)

CA
(1)

CA1127345A
(en)

DE
(1)

DE2734237A1
(en)

FR
(1)

FR2360620A1
(en)

GB
(1)

GB1590412A
(en)

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(1)

SE7708525L
(en)

Cited By (2)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

GB2150938A
(en)

1983-12-05
1985-07-10
Tyndale Plains Hunter Limited
Hydrophilic polyurethane acrylate compositions

GB2194951A
(en)

1986-09-10
1988-03-23
Courtaulds Plc
Production of urethane polymer films

Families Citing this family (4)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

FR2425094B1
(en)

1978-05-01
1985-07-19
Minnesota Mining & Mfg

PHOTOPOLYMERIZABLE COMPOSITIONS

BR8303781A
(en)

1982-07-28
1984-04-24
Goodyear Tire & Rubber

Unsaturated polyurethane and process for its production

JPS60235822A
(en)

1984-05-10
1985-11-22
Toagosei Chem Ind Co Ltd
Curable resin composition

US4771078A
(en)

1985-11-12
1988-09-13
The Goodyear Tire & Rubber Company
Method of producing a foam from a radiation-curable composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party

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Priority date
Publication date
Assignee
Title

DE2443786C2
(en)

1974-09-13
1984-01-19
Basf Ag, 6700 Ludwigshafen

Liquid, photo-crosslinkable molding compound for the production of relief printing plates

1977

1977-07-22
GB
GB3081477A
patent/GB1590412A/en
not_active
Expired

1977-07-25
SE
SE7708525A
patent/SE7708525L/en
not_active
Application Discontinuation

1977-07-27
AU
AU27361/77A
patent/AU516173B2/en
not_active
Expired

1977-07-28
CA
CA283,688A
patent/CA1127345A/en
not_active
Expired

1977-07-29
DE
DE19772734237
patent/DE2734237A1/en
not_active
Withdrawn

1977-08-01
JP
JP9245977A
patent/JPS5317694A/en
active
Pending

1977-08-01
FR
FR7723611A
patent/FR2360620A1/en
not_active
Withdrawn

Cited By (3)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

GB2150938A
(en)

1983-12-05
1985-07-10
Tyndale Plains Hunter Limited
Hydrophilic polyurethane acrylate compositions

GB2194951A
(en)

1986-09-10
1988-03-23
Courtaulds Plc
Production of urethane polymer films

GB2194951B
(en)

1986-09-10
1990-01-10
Courtaulds Plc
Production of urethane polymer films

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AU2736177A
(en)

1979-02-01

DE2734237A1
(en)

1978-02-09

SE7708525L
(en)

1978-02-03

CA1127345A
(en)

1982-07-06

JPS5317694A
(en)

1978-02-17

FR2360620A1
(en)

1978-03-03

AU516173B2
(en)

1981-05-21

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