US 3,984,606 AGrant
Curable Polyene-Polythiol Hydantoin Coating Compositions
Issue Date:1976-10-05
•4 Claims
Abstract
A curable composition comprising compatible polyene and polythiol in which both the components are derived from a hydantoin glycol. The polyene is typically a reaction product of N,N'-bis-(2-hydroxyethyl) dimethylhydantoin, a diisocyanate and an unsaturated alcohol, e.g., allyl alcohol. The polythiol is typically a reaction product of N,N'-bis(2-hydroxyethyl) dimethylhydantoin and a mercapto carboxylic acid, e.g., .beta.-mercaptopropionic acid. Upon exposure to a free radical generator, e.g., actinic radiation, this polyene-polythiol composition cures to solid, insoluble, chemically resistant, cross-linked polythioether products.
Metadata
Assignee
- W. R. Grace & Co.
Inventor
- Charles R. Morgan
Application Information
Application Number:US 6150047
Filing Date:1975-09-19
Priority Date:1974-04-15
Art Unit:142
Classifications
IPC:
C08F 246C08F 818
Field of Search:
204260427428159.15;159.18;159.22;159.23;159.2477.5 BB;77.5 AP;47 CB54419;425;457
Patent Drawings
This patent does not have any drawings.
Description
Example I
To a 3,000 ml. resin kettle equipped with stirrer, thermometer, nitrogen inlet and outlet and vented addition funnel was charged under a nitrogen blanket 959.4 grams of commercially available trimethylolpropane diallyl ether and 0.98 grams of stannous octoate catalyst. 1,000 grams of commercially available isophorone diisocyanate was charged to the addition funnel and added dropwise to the kettle with stirring over a 41/2 hour period while maintaining the temperature below 70.degree. C. After the isophorone diisocyanate was completely added, the temperature was allowed to drop to room temperature (24.degree. C), the nitrogen blanket discontinued and the reaction was stirred for 48 hours.
To a separate 1,000 ml. resin kettle equipped with stirrer, thermometer, nitrogen inlet and outlet and vented addition funnel was charged 535 grams of the reaction product from above along with 16 drops of stannous octoate. 301.3 grams of commercially available pentaethoxylated N,N'-bis(2-hydroxyethyl) dimethylhydantoin was charged to the addition funnel and thereafter added dropwise to the resin kettle with stirring while maintaining the temperature below 70.degree. C. The resultant polyene product of the formula: ##SPC3##
wherein m + n equals 7 and the polyene product had a carbon to carbon unsaturation content of 2.9 mmoles/g.
This polyene will be referred to hereinafter as Polyene A.
Example Ii
To a 3,000 ml. resin kettle equipped with stirrer, thermometer, nitrogen inlet and outlet and vented addition funnel was charged under a nitrogen blanket 261 grams of commercially available tolylene diisocyanate. 87 grams of commercially available allyl alcohol was added to the addition funnel and thereafter added dropwise to the resin kettle with stirring while maintaining the temperature below 85.degree. C. After 11/2 hours the addition was complete and the reaction was stirred for an additional 11/2 hours at which time the isocyanate was analyzed and was found to be 4.26 meq./g.
325 grams of the reaction product was transferred to a 200 ml. resin kettle similarly equipped as above and containing 400 ml. chloroform and 0.25 gram stannous octoate. 151.3 grams of commercially available N,N'-bis(2-hydroxyethyl) dimethylhydantoin was added to the resin kettle and a definite exotherm was noted. The NCO band in the IR was followed until disappearance. The material was transferred to a blender and petroleum ether was added to precipitate the product as a fine white powder. The powder was filtered and dried in vacuo. It contained a carbon-to-carbon unsaturation of 2.7 mmoles/g. This resulting polyene has the formula: ##SPC4##
This polyene will hereinafter be referred to as Polyene B.
Example Iii
To a 1,000 ml. resin kettle equipped with stirrer, thermometer, nitrogen inlet and outlet and vented addition funnel was charged 294.8 grams of commercially available tolylene diisocyanate. 365.2 grams of trimethylolpropane diallyl ether was charged to the addition funnel and thereafter added dropwise to the resin kettle under a nitrogen atmosphere while maintaining the temperature below 28.degree. C. After the addition was complete the material was stirred for about 4 hours. The material had a NCO content of 2.47 meq./g.
To another 1,000 ml. resin kettle equipped with stirrer, thermometer, nitrogen inlet and outlet and an addition funnel was charged 200 grams of commercially available pentadecaethoxylated N,N'-bis(2-hydroxyethyl) dimethylhydantoin having an OH content of 1.95 meq./g. along with 3 drops of stannous octoate. 157.2 grams of the reaction product of the tolylene diisocyanate and the trimethylolpropane diallyl ether reaction supra was charged to the addition funnel and thereafter added dropwise to the resin kettle. The temperature was maintained below 58.degree. C. during the 41/2 hours of addition. The reaction was stirred for an additional 21 hours during which time the NCO content was monitored by IR scans. The resultant polyene had a carbon to carbon unsaturation of 2.35 mmoles/g. and had the formula: ##SPC5##
wherein m + n is 17.
This polyene will hereinafter be referred to as Polyene C.
Example Iv
Example III was repeated except that 226 grams of the reaction product of tolylene diisocyanate and trimethylolpropane diallyl ether was added to 200 grams of commercially available decaethoxylated N,N'-bis(2-hydroxyethyl)dimethylhydantoin. The resultant polyene had a C=C content of 2.72 meq./g. and had the formula: ##SPC6##
wherein m + n is 12.
This polyene will hereinafter be referred to as Polyene D.
Example V
Example III was repeated except that 326 grams of the reaction product of tolylene diisocyanate and trimethylolpropane diallyl ether was added to 200 grams of commercially available pentaethoxylated N,N'-bis(2-hydroxyethyl) dimethylhydantoin. The resultant polyene had a carbon to carbon unsaturation of 3.17 mmoles/g. and had the formula: ##SPC7##
wherein m + n is 7.
This polyene will hereinafter be referred to as Polyene E.
Example Vi
To a 3,000 ml. resin kettle equipped with stirrer, thermometer, nitrogen inlet and outlet and addition funnel was charged under a nitrogen blanket 250 grams of commercially available tolylene diisocyanate along with 0.28 grams of stannous octoate catalyst. 323.14 grams of diallyl malate was charged to the addition funnel and thereafter added dropwise to the resin kettle with stirring while maintaining the temperature below 58.degree. C. The reaction was continued for 4 hours. 529 grams of the reaction product was transferred to a dropping funnel and thereafter added dropwise to a 2,000 ml. resin kettle containing 147.4 grams of commercially available N,N'-bis(2-hydroxyethyl) dimethylhydantoin and 0.39 grams stannous octoate. The reaction thickened as addition continued and the temperature was allowed to rise to about 100.degree. C to permit stripping. An additional 0.39 grams of stannous octoate was added to the reaction and the reaction was continued for 51 hours at which time the IR scan showed zero NCO. The resultant polyene had a C=C content of 4.06 mmoles/g. and was of the formula: ##SPC8##
This polyene will hereinafter be referred to as Polyene F.
The following examples show the preparation of a polythiol derived from a hydantoin glycol.
Example Vii
To a 2,000 ml. 3-necked flask equipped for distillation with stirrer and nitrogen inlet was charged 432 grams (2 moles) of commercially available N,N'-bis(2-hydroxyethyl) dimethylhydantoin, 445 grams of mercaptopropionic acid and 17.5 grams p-toluenesulfonic acid. 100 ml. of ethylene dichloride was added to the flask. The mixture was heated with stirring for 8 hours and the evolved water was continuously removed by azeotropic distillation at 71.degree.-75.degree. C, returning the ethylene dichloride to the reaction flask. The solution in the flask was then washed once with about 1,000 ml. water, twice with about 1,000 ml. of 5 percent sodium bicarbonate and finally with about 1,000 ml. of water. The solution was dried over anhydrous magnesium sulfate, mixed with 10 g. of decolorizing carbon and filtered. The solvent was removed by vacuum distillation, affording 672 g. of product or an 86 percent yield of the following polythiol: ##SPC9##
This polythiol will be referred to hereinafter as Polythiol Z.
Example Viii
To a 2 liter, 3-necked, round-bottom flask equipped with stirrer, thermometer, Dean-Stark trap and reflux condenser was charged 216 grams of commercially available N,N'-bis(2-hydroxyethyl) dimethylhydantoin, 193.2 grams of thioglycollic acid, 8.18 grams of p-toluenesulfonic acid and 500 ml. of benzene. The mixture was heated to reflux temperature with stirring. The amount of water collected in the Dean-Stark trap was periodically determined and the reaction was stopped when 39.5 ml. water was collected. The mixture was cooled to room temperature, washed with 500 ml. water then twice washed with 500 ml. of a 5 percent NaHCO.sub.3 solution followed by an additional 500 ml. water wash. The benzene layer was removed and dried over 60 grams anhydrous MgSO.sub.4. 2.5 grams decolorizing carbon was then added to the mixture and it was filtered through a fritted filter with the aid of a vacuum. The benzene was stripped off under high vacuum in a flash evaporator to give the polythiol in the amount of 293 grams (80.5 percent yield). On analysis the product had an SH content of 4.96 meq. SH/g., a COOH content of 0.02 meq. COOH/g. and an ester content of 6.07 meq. ester/g. The polythiol had the formula: ##SPC10##
The following examples show the ability of the polyenes and polythiols herein to form cured polythioethers on exposure to actinic radiation. The polyenes and polythiols herein when cured together result in cured materials having a high percent of elongation on failure as compared to other commercially available polyenes and polythiols.
Example Ix
The following formulations were prepared in 200 ml. brown sample bottles. In all cases accurately weighed amounts of the polyene, stabilizers, photosensitizer and polythiol were added to the bottle and admixed until homogeneous before use. When Polyene A (a solid at room temperature 25.degree. C) was used in the formulation, it was heated to 80.degree. C in order to facilitate weighing and handling.
Each formulation was poured on a glass plate and drawn down to a 20 mil thick film. The film on the plate was exposed to UV radiation for 2 minutes under a UV Ferro lamp at a surface intensity of 7,000 microwatts/cm.sup.2. The cured samples were measured for percent elongation at failure. The results are shown in Table I.
As can be seen from the results, formulations D and H, consisting of the polyene and polythiol in which both components are derived from a hydantoin glycol, resulted in cured polythioethers having very high percent elongations as compared to the polyenes herein used with commercially available mercaptate esters.
The molecular weight of the polyenes and polythiols of the present invention may be measured by various conventional methods including solution viscosity, osmotic pressure and gel permeation chromatography. Additionally, the molecular weight may be calculated from the known molecular weight of the reactants.
As can be seen from the above detailed description, the subject curable and particularly photocurable compositions comprised of compatible polyenes and polythiols derived from hydantoin glycol exhibit extremely satisfactory chemical and physical properties and are versatile curable polymeric systems.
It is understood that the foregoing detailed description is given merely by way of illustration and that many variations may be made therein without departing from the spirit of this invention.
Claims
What is claimed is:
1. A process which comprises applying to the surface of a substrate a layer of a curable composition useful for obtaining a solid crosslinked polythioether comprising: 1. A polyene of the formula: ##SPC11## wherein A and B are polyvalent organic radical members free of reactive carbon to carbon unsaturation and are independently selected from the group consisting of aryl, substituted aryl, aralkyl, substituted aralkyl, cycloalkyl, substituted cycloalkyl, alkyl and substituted alkyl containing 1 to 36 carbon atoms and mixtures thereof, said group members can be connected by a chemically compatible linkage selected from the group consisting of --O--, --S--, carboxylate, carbonate, carbonyl, urethane and substituted urethane, urea and substituted urea, amide and substituted amide, amine and substituted amine and hydrocarbon; Z is a divalent chemically compatible linkage selected from the group consisting of ##EQU1## --O-- and --S--; X is a member selected from the group consisting of (a) --(CH.sub.2).sub.d --CR'=CHR, (b) --O--(CH.sub.2).sub.d --CR'=CHR, (c) --S--(CH.sub.2).sub.d --CR'=CHR, (d) --(CH.sub.2).sub.d --C.tbd.CR, (e) --O--(CH.sub.2).sub.d --C.tbd.CR, (f) --S--(CH.sub.2).sub.d --C.tbd.CR; and mixtures thereof; where R and R' each are independently selected from the group consisting of hydrogen and methyl radicals; d, p and q are each integers from 0 to 1; m and n are each integers of at least 1; with m + n from 2 to 22 and r at least 1, and y from 1 to 10; and 2.
2. A polythiol of the formula: ##SPC12## wherein m and n are each at least 1 and m + n is 2 to 22 and R.sub.3 is a polyvalent organic radical member free of reactive carbon-to-carbon unsaturation and is selected from the group consisting of aryl, substituted aryl, aralkyl, substituted aralkyl, cycloalkyl, substituted cycloalkyl, alkyl and substituted alkyl groups containing 1 to 16 carbon atoms and mixtures thereof, the total combined functionality of (a) the reactive carbon to carbon bonds per molecule in the polyene and (b) the thiol groups per molecule in the polythiol being greater than 4 and, thereafter, exposing the layer to ambient conditions in the presence of a free radical generator thereby curing said composition. 2. The process according to claim 1 wherein at least the surface of said substrate is metallic.
3. An article comprising a substrate coated with a curable composition useful for obtaining a solid crosslinked polythioether comprising: 1. A polyene of the formula: ##SPC13## wherein A and B are polyvalent organic radical members free of reactive carbon to carbon unsaturation and are independently selected from the group consisting of aryl, substituted aryl, aralkyl, substituted aralkyl, cycloalkyl, substituted cycloalkyl, alkyl and substituted alkyl containing 1 to 36 carbon atoms and mixtures thereof, said group members can be connected by a chemically compatible linkage selected from the group consisting of --O--, --S--, carboxylate, carbonate, carbonyl, urethane and substituted urethane, urea and substituted urea, amide and substituted amide, amine and substituted amine and hydrocarbon; Z is a divalent chemically compatible linkage selected from the group consisting of ##STR13## --O-- and --S--; X is a member selected from the group consisting of (a) --(CH.sub.2).sub.d --CR'=CHR, (b) --O--(CH.sub.2).sub.d --CR'=CHR, (c) --S--(CH.sub.2).sub.d --CR'=CHR, (d) --(CH.sub.2).sub.d --C.tbd.CR, (e) --O--(CH.sub.2).sub.d --C.tbd.CR, (f) --S--(CH.sub.2).sub.d --C.tbd.CR; and mixtures thereof; where R and R' each are independently selected from the group consisting of hydrogen and methyl radicals; d, p and q are each integers from 0 to 1; m and n are each integers of at least 1; with m + n from 2 to 22 and r at least 1, and y from 1 to 10; and 2. A polythiol of the formula: ##SPC14## wherein m and n are each at least 1 and m + n is 2 to 22 and R.sub.3 is a polyvalent organic radical member free of reactive carbon-to-carbon unsaturation and is selected from the group consisting of aryl, substituted aryl, aralkyl, substituted aralkyl, cycloalkyl, substituted cycloalkyl, alkyl and substituted alkyl groups containing 1 to 16 carbon atoms and mixtures thereof, the total combined functionality of (a) the reactive unsaturated carbon to carbon bonds per molecule in the polyene and (b) the thiol groups per molecule in the polythiol being greater than 4.
4. The article according to claim 3 wherein the composition contains a photocuring rate accelerator.
Patent Citations (3)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US3697395 | 1972-10-01 | Kehr et al. | |
| US3839354 | 1974-10-01 | Habermeier | |
| US3945982 | 1976-03-01 | Morgan |