Patent Application
20210130543
The present disclosure provides a method for the synthesis of cyanurate-multifunctional alcohol, polyether (meth)acrylate for UV curable materials.
UV curing materials are widely used in inks, adhesives, paints, and coatings due to their fast cure rate, energy saving, and less or even no emission of volatile organic chemicals (VOC). Typical UV curable resins consist of oligomers, monomers (which act as diluents), photo-polymerization initiators, co-initiators (spectral sensitizer, reducing agents etc.) and various additives such as stabilizers, antioxidants, plasticizers, and pigments. The majority of commercial light curable resins are based on free radical curing acrylic compounds (acrylates). Free radical curing compositions are the most versatile curing systems in regard to product properties and monomers/oligomers available on the market.
At present, a large number of acrylic-functionalized oligomers presently commercially available are based on polyesters, epoxy resins, aliphatic and aromatic urethanes, and silicones. These polymers usually have a high viscosity, needing diluent to reduce the viscosity in order to facilitate surface spreading in coatings, inks and adhesives. Urethane acrylate oligomers as UV curable prepolymers are available in large quantities and can be synthesized through multi-step reactions of diisocyantes, hydroxylalkyl acrylates, and polyether based polyols through two approaches. In one approach the difunctional polyether polyol first reacts with two molecules of diisocyanate on each chain end to produce an isocyanate terminated polymer, after which the chain ends are capped with a hydroxy functional acrylate through direct addition.
The other approach is that one molecule of diisocyanate is first reacted with one molecule of hydroxy functional acrylate to produce a monomer with an isocyanate at one chain end and an acrylate at the other chain end, after which two moles of bifunctional monomers are reacted with one mole of bifunctional polyether polyol to produce acrylate terminated oligomer. The polyether based polyols are synthesized by ring opening polymerization of propylene oxide with multifunctional alcohol starting agents. Although there are some obvious advantages of using poly(propylene oxide) polyether, such as no coloration, good resilience, and easy spreading on surfaces due to low viscosity, poly(propylene oxide) polyether acrylate type of UV curing materials are not available due to the difficulty involved in their synthesis.
Polypropylene oxide polyols are widely used in the synthesis of polyurethane and other materials. The synthesis of poly(propylene oxide) polyols have been widely investigated, and are still a hot research area. Synthesis of low molecular weight multifunctional poly(propylene oxide) polyols (hydroxyl number 200 mgKOH/g) are mostly achieved by polymerizing propylene oxide with multifunctional polyol starting agents in the presence of alkaline catalysts mostly potassium hydroxide.
Synthesis of high molecular weight poly(propylene oxide) polyols are achieved by chain extension through ring opening polymerization of propylene oxide of the above polymer using double metal catalysts or other catalysts. Due to the softness of poly(propylene oxide) polyether, low molecular weight products are more suitable for the preparation of stiff and resilient materials such as coatings, adhesives, inks, 3D printing. High molecular weight poly(propylene oxide) polyether is more suitable for rubbery materials. To further increase the stiffness or mechanical strength, rigid starting agents may be used. Cyanuric acid is known for its rigid ring and good thermal stability and mechanical strength, and has been used for a variety of material construction. The excellent thermal and mechanical properties of isocyanurate based polypropylene oxide ether polyurethane materials were reported long time ago. 1,3,5-Tris(2-hydroxyethyl)cyanuric acid triacrylate (CAS No. 40220-08-4) are widely used as curing agent showing excellent thermal stability and chemical resistance. However, its high melting point restricts its wide application. Due to the insolubility of cyanuric acid, the synthesis of isocyanurate based poly(propylene oxide) polyols directly using cyanuric acid as starting material has not been reported.
Two main approaches are used to synthesize (meth)acrylate products: direct esterification of (meth)acrylic acid with alcohols and transesterification of low alcohol (meth)acrylates such as methyl (meth)acrylate or ethyl (meth)acrylate with higher alcohols. Both direct esterification and transesterification are equilibrium reactions. To shift the reaction towards high alcohol (meth)acrylate products, the byproducts of water and/or low alcohols must be removed from the reaction mixture either by azeotropic distillation using an azeotropic solvent or by adsorption with an absorbent. Both of these methods of direct esterification and transesterification methods work well with primary alcohols. However, secondary alcohols are much less reactive and tertiary alcohols are unreactive towards direct esterification and transesterification because of steric hindrance. Thus, higher reaction temperature and longer reaction time are needed for the synthesis of esters of secondary alcohols. (Meth)acrylic acid and esters are very temperature sensitive chemicals, liable to radical polymerization under long time heating. The inhibition of their auto radical polymerization has been a long time research topic, see (Chen. Eng. Technol. 2006, 29 (8), 931-936).
Polymerization can happen on the reactor wall, reflux condenser, and distillation column. There have been many accidents involved in these processes even related to the melting of glacial acrylic acid. The reaction conditions for the synthesis of various acrylates depends on the reactivity and properties of feedstock.
Ring opening polymerization of propylene oxide produces polyether polyols with mainly secondary alcohols at the chain end. Many researchers have attempted to synthesize poly(propylene oxide) acrylates through direct esterification or transesterification of polypropylene oxide polyols, but have not been successful due to the low reactivity of the secondary alcohols of polypropylene oxide and the likely radical polymerization of acrylic acid and polyether acrylates at elevated temperature for extended reaction time. Auto polymerization of acrylic acid and acrylates also frequently happened during experiments carried out by the present inventors. In the polyurethane industry, to increase the reactivity of poly(propylene oxide) polyol, ethylene oxide end capping is used to produce polyether polyols with high percentage of primary alcohol chain ends, but the end capping can only produce 85% primary alcohols at the chain ends, the 15% secondary alcohol still has difficulty in esterification. What is more, for low molecular weight poly(propylene oxide) polyether, end capping with poly(ethylene oxide) will greatly modify the properties of the polyether product to give unwanted high hydroscopic and crystalline characters. Although the synthesis of polyethylene glycol (meth)acrylates through direct esterification or transesterification of the primary alcohols in polyethylene oxide polyols are well documented, there are some limitations in applications of the hydroscopic and crystalline polyethylene oxide.
The present disclosure provides a method for synthesis of cyanurate-glycerol polyether acrylate for UV curable materials.
The present disclosure provides a multifunctional polyether polyol which is a polymerization product of:
cyanuric acid or substituted cyanuric acid,
The substituted cyanuric acid may be 1,3,5-Tris(2-hydroxyethyl)cyanuric acid.
The polyether polyol may have the following general formula:
wherein each of x, y, and z is independently 1 to 20.
The multifunctional alcohol may be glycerol or sucrose.
The polymerization product may further include triethanolamine units.
The polyether polyol may have a molecular weight in a range from about 300 to about 2000 g/mol.
The present disclosure provides polymer which is an esterified product of (i) the polyether polyol and (ii) any one or a combination of acrylic acid, methacrylic acid, acrylate and methacrylate. The acrylate may be ethyl acrylate or methyl acrylate, and the methacrylate is methyl methacrylate or ethyl methacrylate.
The present disclosure provides a UV curable composition comprising these polymers. These UV curable compositions may be for use in any one of coatings, adhesives, paints, printing inks, and 3D printing.
The present disclosure provides a method of preparing a trifunctional polyether polyol, the method comprising:
mixing monomers in a reactor in the presence of a catalyst to obtain a mixture of the monomers, wherein the monomers in the mixture comprise cyanuric acid or substituted cyanuric acid, multifunctional alcohol, and propylene oxide; and
polymerizing the monomers in the reactor to produce the trifunctional polyether polyol.
The monomers may further comprise triethanolamine. The substituted cyanuric acid may be 1,3,5-Tris(2-hydroxyethyl)cyanuric acid.
The cyanuric acid or the substituted cyanuric acid may be present in the amount of about 0 to about 60 mol %, and the triethanolamine is in the range from about 0 to about 20 mol %.
The multifunctional alcohol may be glycerol or sucrose.
The catalyst may be an alkaline catalyst.
The alkaline catalyst may be potassium hydroxide or sodium hydroxide. The catalyst may be present in a concentration from about 0.1 to about 5 mol % of hydroxyl groups.
The multifunctional polyether polyol may be a trifuctional trifunctional polyether polyol. The concentration of the catalyst may be in a range from about 0.2 to about 3 mol % of hydroxyl groups.
The present disclosure provides a method of preparing a polyether polyol (meth)acrylate comprising:
adding the multifunctional polyether polyol according to the present disclosure into a reactor; and
reacting the trifunctional polyether polyol with an esterification agent in the presence of a catalyst, wherein the esterification agent is selected from the group consisting of acrylic acid, methacrylic acid, low alcohol acrylate, and low alcohol methacrylate.
The polyether polyol may be glycerol isocyanurate poly(propylene oxide) polyether polyol, glycerol-triethanolamine-isocyanurate poly(propylene oxide) polyether polyols, sucrose-glycerol poly(propylene oxide) polyether polyols, sucrose-glycerol-triethanolamine poly(propylene oxide) polyether polyols.
The esterification agent used in the reacting step may be low alcohol acrylate or low alcohol methacrylate, selected from the group consisting of methyl acrylate, ethyl acrylate, methyl methacrylate and ethyl methacrylate.
The catalyst may be titanium tetrachloride (TiCl4) or titanium tetraiosproppoxide (TiTIP). The TiCl4 may be present in a concentration of about 0.1 to about 2 wt % and TiTIP may be present in a concentration range from about 0.1 to about 2 wt %.
The method may further include a step of recycling the catalyst for a next reaction without sacrifice their activity.
The ratio of the esterification agent and hydroxyl groups in the polyether polyol may be about 1.0 to about 5.0:1. The ratio may be about 1.2 to about 2.5:1.
The method may further comprise adding a solvent wherein the solvent is any one or a combination of a hydrocarbon solvent and an ether solvent. The hydrocarbon solvent may be any one of hexanes, cyclohexane, heptane, octane and toluene, and the ether solvent is any one of dioxane, dimethyl ethylene glycol ether, diethyl ethylene glycol ether, and dimethyl propylene glycol ether.
The method may further comprise a step of removing by-product methanol or ethanol. This removing step may be carried out using molecular sieves or azeotropic distillation.
The method may further comprise a step of adding an inhibitor for polymerization of the esterification agents. The inhibitor may be any one or a combination of phenothiazine, methyl hydroquinone (MEDQ), diethylhydroxylamine and nitrosobenzene.
The esterification agent used in the reacting step may be acrylic acid or methacrylic acid. The catalyst may be organosulfonic acid. This organosulfonic acid may be any one of toluenesulfonic acid, methanesulfonic acid, and sulfonic based ionic exchange resins. The toluenesulfonic acid or the mathanesulfonic acid may be added in a concentration range from about 0.1 to about 3 wt %. The sulfonic based ionic exchange resins may be added in a concentration from about 2 to about 30 wt %.
The method may further comprise a step of adding a polymerization inhibitor and/or a water-azeotropic solvent. This polymerization inhibitor may be a phenolic antioxidant or phenothiazine. The phenolic antioxidant may be methyl hydroquinone (MEHQ) or butylate hydroxytoluene (BHT).
The phenolic antioxidant may be added in a concentration range of about 100 to about 10,000 ppm and the phenothiazine may be added in a concentration of about 100 to about 5,000 ppm.
The polymerization inhibitor may be added to a Dean Stark to prevent advent polymerization on a fractional column.
The solvent may be any one or a combination of a hydrocarbon and chlorinate hydrocarbon. The hydrocarbon may be a hexane, a cyclohexane or a heptane, and the chlorinate hydrocarbon may be 1,2-dichloroethane, 1,1-dichlorethane or chloroform.
A further understanding of the functional and advantageous aspects of the present disclosure can be realized by reference to the following detailed description and drawings.
Embodiments disclosed herein will be more fully understood from the following detailed description thereof taken in connection with the accompanying drawings, which form a part of this application, and in which:
Various embodiments and aspects of the disclosure will be described herein with reference to details discussed below. The following description and drawings are illustrative of the disclosure and are not to be construed as limiting the disclosure. The drawings are not to scale. Numerous specific details are described to provide a thorough understanding of various embodiments of the present disclosure. However, in certain instances, well-known or conventional details are not described in order to provide a concise discussion of embodiments of the present disclosure.
As used herein, the terms “comprises” and “comprising” are to be construed as being inclusive and open ended, and not exclusive. Specifically, when used in the specification and claims, the terms “comprises” and “comprising” and variations thereof mean the specified features, steps or components are included. These terms are not to be interpreted to exclude the presence of other features, steps or components.
As used herein, the terms “about” and “approximately” are meant to cover variations that may exist in the upper and lower limits of the ranges of values, such as variations in properties, parameters, and dimensions.
Disclosed herein is a method for the synthesis of cyanurate-multifunctional alcohol based, especially cyanurate-glycerol polyether (meth)acrylate and isocyanurate-glycerol-triethanolamine polyether (meth)acrylates for UV curable materials. The inventors have synthesized a special type of polyether (meth)acrylates which is not available in the present market, that is, isocyanurate-glycerol based polyether (meth)acrylates. Compared with present polyethers in the market which are mostly aliphatic polyol based, isocyanurate-glycerol based polyethers have rigid isocyanurate structure, endowing the material extra strength and thermal stability. The triethanolamine unit in isocyanurate-glycerol-triethanolamine polyether (meth)acrylates endows the material with anti-oxygen inhibition property in UV curing process. The isocyanurate-glycerol based polyether (meth)acrylates have low viscosity and high reactivity towards UV cure. The cured resins have high resilience and strength. Thus, isocyanurate-glycerol based polyether (meth)acrylates will have wide applications in UV curable adhesives, coatings, inks, sealants, paints, 3D printing. The applications are literally unlimited.
The present disclosure mainly includes three key discoveries: 1) the unique method for the synthesis of trifunctional cyanurate-glycerol-poly(propylene oxide) polyether polyols (CGPE, Examples 4, 5, 6 below), 2) synthesis of polyether (meth)acrylates including cyanurate-glycerol-poly(propylene oxide) polyether (meth)acrylates through transesterification (Examples 7, 8, 9 below), synthesis of polyether (meth)acrylates including cyanurate-glycerol-poly(propylene oxide) polyether acrylates through direct esterification (Examples 10, 11, 12 below).
The process may be described by Scheme 1 shown below.
Scheme 1 shows the synthesis of cyanuric-glycerol polyether and three functional acrylate UV curable resin.
The following non-limiting examples give some detailed description of the disclosure, but the scope of the disclosure cannot be limited in the examples.
8.60 g 85% potassium hydroxide was dissolved in 15.00 g distilled water, and then mixed with 200.0 g glycerol in a flask. The mixture is evaporated to remove water through rotary evaporator. The obtained mixture was used for the synthesis of poly (propylene oxide) with different KOH contents.
The Production of Glycerol Poly(Propylene Oxide) Ether Polyol-500 (GPE500) 500 g/mol).
6.500 g of the above prepared glycerol-KOH solution and 6.500 g glycerol are added into a parr pressure reactor. The reactor was evacuated and purged with nitrogen several times. Then the reactor heated to around 100° C. 57.75 g propylene oxide is added into the reactor using a pump with the flow rate of 2 ml/min. After that, the reaction temperature is kept at 125° C. for 15 min before cooling down to room temperature. Unreacted propylene oxide was removed by high vacuum evacuation at 35° C. for 2 hours, under 0.10 g loss was found, showing complete conversion of propylene oxide.
11.12 g sucrose, 8.70 g glycerol-KOH solution and 0.500 g glycerol are added into a batch reactor. Nitrogen is used to remove the air in the reactor for three times. Then 20.00 g propylene oxide is added into reactor though a pump and the reaction temperature is increased to around 90° C. for 30 mins. After that, the reaction temperature is increased to around 120 to 130° C. with the addition of 42.60 g propylene oxide at a flow rate of 2 ml/min. The reaction temperature is kept at 130° C. for 30 mins before cooling down to room temperature. Complete conversion of propylene oxide was achieved.
6.58 g cyanuric acid, 4.10 g of the above prepared glycerol-KOH solution and 7.20 glycerol are added into a batch reactor. Nitrogen was used to remove the air in the reactor for three times and then the reaction temperature was increased to around 120 to 130° C. Next, the 67.27 g propylene oxide was added into the reactor using a pump with the flow rate of 2 ml/min. The reaction temperature was kept at 130° C. for 60 mins before cooling down to room temperature. Complete conversion of propylene oxide was achieved.
11.75 g 1,3,5-Tris(2-hydroxyethyl)cyanuric acid, 3.60 g of the above prepared glycerol-KOH solution and 6.20 glycerol are added into a batch reactor. Nitrogen was used to remove the air in the reactor for three times and then the reaction temperature was increased to around 120 to 130° C. Next, the 53.50 g propylene oxide was added into the reactor using a pump with the flow rate of 2 ml/min. The reaction temperature was kept at 130° C. for 60 mins before cooling down to room temperature. Complete conversion of propylene oxide was achieved.
Production of (1/3/6 Mol) Triethanolamine-Cyanuric Acid-Glycerol Poly(Propylene Oxide) Ether Polyol TEACGPE 800 g/Mol
1.60 g triethanolamine, 4.14 g cyanuric acid, 2.60 g glycerol-KOH solution and 3.50 glycerol were added into a batch reactor. Nitrogen was used to remove the air in the reactor for three times and then the reaction temperature was increased to around 120 to 130° C. Then, 73.83 g propylene oxide was added into the reactor using a pump with at the flow rate of 2 ml/min. After that, the reaction temperature was kept at 130° C. for 60 mins before cooling down to room temperature. Complete conversion of propylene oxide was achieved.
Synthesis of Trifunctional CGPE Acrylate Through Transesterification with Ethyl Acrylate (EA)
In a 300 mL three-neck flask, one neck was equipped with a pressure balanced addition funnel with a condenser and bubbler on the top. The funnel was filled with 4A molecular sieves. The other two necks were connected with a nitrogen inlet and a thermometer. 60.00 g of the above polyether polyol (molecular weight 500 g/mol) was added, followed by 10.00 g dioxane, 0.35 g titanium tetrachloride, the mixture was stirred for 15 min under nitrogen flow. Then 0.2 g phenothiazine (PTZ) was added, followed by 72.00 g of EA. The mixture was purged with nitrogen for 15 min, then was refluxed at in a 115° C. oil bath with magnetic stirring for 8 hours. After cooling to room temperature, the reaction mixture was diluted with dichloromethane, centrifuged. The solvent and unreacted EA in liquid mixture was removed in a rotary evaporator under vacuum, left the product polyether acrylate in the distillation flask. EA and dioxane as a mixture which can be reused as feedstock for the next reaction was recovered by removing dichlormethane by fractional distillation. The FTIR spectra shown in
Synthesis of Trifunctional CGPE Acrylate Through Transesterification with Methyl Acrylate (MA)
In a 300 mL three-neck flask, one neck was equipped with a pressure balanced addition funnel with a condenser and bubbler on the top. The funnel was filled with 4A molecular sieves. The other two necks were connected with a nitrogen inlet and a thermometer. 60.00 g of the above polyether polyol (molecular weight 500 g/mol) was added, followed by 15.00 g ethylene diethyl ether, 0.25 g titanium tetrachloride, the mixture was stirred for 15 min under nitrogen flow. Then 0.5 g diethylhydroxylamine, 0.1 g phenothiazine (PTZ) was added, followed by 62.00 g of MA. The mixture was purged with nitrogen for 15 min, then was refluxed in a 110° C. oil bath with magnetic stirring for 8 hours. After cooling to room temperature, the reaction mixture was diluted with dichloromethane, centrifuged. The solvent and unreacted MA in liquid mixture was removed in a rotary evaporator under vacuum, left the product polyether acrylate in the distillation flask. MA and ethylene diethyl ether as a mixture which can be reused as feedstock for the next reaction was recovered by removing dichlormethane by fractional distillation. FTIR spectrum shows almost complete conversion of the hydroxyl groups to acrylate groups.
Synthesis of Trifunctional CGPE Acrylate Through Transesterification with Methyl Acrylate (MA)
In a 250 mL three-neck flask, one neck was equipped with a fractional column with Dean Stark, a condenser and bubbler sequentially on the top. The dean Stark was filled with a solution of 0.5% diethylhydroxylamine in hexanes. The fractional column is filled with glass spring. The other two necks were connected with a nitrogen inlet and a thermometer. 60.00 g of the above polyether polyol (molecular weight 500 g/mol) was added, followed by 5.00 g hexanes, 15.00 g ethylene diethyl ether, 0.25 g titanium tetrachloride, the mixture was stirred for 15 min under nitrogen flow. Then 0.1 g phenothiazine (PTZ) was added, followed by 62.00 g of MA. The mixture was purged with nitrogen for 15 min, then was refluxed in a 110° C. oil bath with magnetic stirring for 8 hours. After cooling to room temperature, the reaction mixture was diluted with dichloromethane, centrifuged. The solvent and unreacted MA in liquid mixture was removed in a rotary evaporator under vacuum, left the product polyether acrylate in the distillation flask. MA and ethylene diethyl ether as a mixture which can be reused as feedstock for the next reaction was recovered by removing dichlormethane by fractional distillation. FTIR spectrum shows almost complete conversion of the hydroxyl groups to acrylate groups.
Synthesis of Trifunctional CGPE Acrylate Through Direct Esterification with Acrylic Acid (AA)
In a 300 mL three-neck flask, one neck was equipped with a fractional column with a Dean Stark, a condenser, and bubbler on the top. The Dean Stark was filled with butylated hydroxyl toluene dissolved in cyclohexane. The other two necks were connected with a gas inlet and a thermometer. 60.00 g of the polyether polyol (molecular weight 500 g/mol) was added, followed by 20.00 g cyclohexane, 1.0 g methyl hydroquinone, 3.0 g toluenesulfonic acid, and 52.0 g acrylic acid. The mixture was refluxed in a 110° C. oil bath with magnetic stirring for 6 hours at 2 ml/min air flow. After cooling to room temperature, the reaction mixture was diluted with dichloromethane, neutralized with potassium carbonate, and centrifuged. The solvent and unreacted AA in liquid mixture was removed in a rotary evaporator under vacuum, left the product polyether acrylate in the distillation flask. AA and cyclohexane as a mixture which can be reused as feedstock for the next reaction was recovered by removing dichlormethane by fractional distillation. FTIR spectrum shows almost complete conversion of the hydroxyl groups to acrylate groups.
Synthesis of Trifunctional CGPE Acrylate Through Direct Esterification with Acrylic Acid (AA)
In a 300 mL three-neck flask, one neck was equipped with a fractional column with a Dean Stark, a condenser, and bubbler on the top. The Dean Stark was filled with phenothiazine dissolved in cyclohexane. The other two necks were connected with a gas inlet and a thermometer. 60.00 g of the polyether polyol (molecular weight 500 g/mol) was added, followed by 20.00 g cyclohexane, 0.1 g phenothiazine, 3.0 g toluenesulfonic acid, and 52.0 g acrylic acid. The mixture was refluxed in a 110° C. oil bath with magnetic stirring for 6 hours at 2 ml/min nitrogen flow. After cooling to room temperature, the reaction mixture was diluted with dichloromethane, neutralized with potassium carbonate, and centrifuged. The solvent and unreacted AA in liquid mixture was removed in a rotary evaporator under vacuum, left the product polyether acrylate in the distillation flask. AA and cyclohexane as a mixture which can be reused as feedstock for the next reaction was recovered by removing dichlormethane by fractional distillation. FTIR spectrum shows almost complete conversion of the hydroxyl groups to acrylate groups.
Synthesis of Trifunctional CGPE Acrylate Through Direct Esterification with Acrylic Acid (AA)
In a 300 mL three-neck flask, one neck was equipped with a fractional column with a Dean Stark, a condenser, and bubbler on the top. The Dean Stark was filled with phenothiazine dissolved in cyclohexane. The other two necks were connected with a gas inlet and a thermometer. 60.00 g of the polyether polyol (molecular weight 500 g/mol) was added, followed by 20.00 g cyclohexane, 0.1 g phenothiazine, 10.00 g Amberlyst 15, and 52.0 g acrylic acid. The mixture was refluxed in a 110° C. oil bath with magnetic stirring for 6 hours at 2 ml/min nitrogen flow. After cooling to room temperature, the reaction mixture was diluted with dichloromethane, filtered. The Amberlyst can be reused. The solvent and unreacted AA in liquid mixture was removed in a rotary evaporator under vacuum, left the product polyether acrylate in the distillation flask. AA and cyclohexane as a mixture which can be reused as feedstock for the next reaction was recovered by removing dichlormethane by fractional distillation. FTIR spectrum shows almost complete conversion of the hydroxyl groups to acrylate groups. The synthesized poly(propylene oxide) polyether acrylates have a viscosity range of 100 cP to 200 cP, so they can be used directly as UV curing materials. Examples 6-11 for the synthesis of polyether acrylates can apply for all the polyether polyols synthesized in examples 1-5.
Various of poly(propylene oxide) polyether acrylates were mixed with 3% UV initiator 2-Hydroxy-2-methylpropiophenone (Daracure 1173, or 1173) and cured under 600 watt UN light. The results show that polyether acrylate products with isocyanurate unit having higher strength, and triethanolamine provides anti-oxygen inhibition effect. (no data).
The foregoing description of the preferred embodiments of the disclosure has been presented to illustrate the principles of the disclosure and not to limit the disclosure to the particular embodiment illustrated. It is intended that the scope of the disclosure be defined by all of the embodiments encompassed within the following claims and their equivalents.
| Number | Date | Country | |
|---|---|---|---|
| 62927876 | Oct 2019 | US |
