CN112250831B - UV resin and preparation method thereof - Google Patents

UV resin and preparation method thereof Download PDF

Info

Publication number
CN112250831B
CN112250831B CN202011083798.2A CN202011083798A CN112250831B CN 112250831 B CN112250831 B CN 112250831B CN 202011083798 A CN202011083798 A CN 202011083798A CN 112250831 B CN112250831 B CN 112250831B
Authority
CN
China
Prior art keywords
monomer
resin
reaction
formula
polycarbonate diol
Prior art date
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.)
Active
Application number
CN202011083798.2A
Other languages
Chinese (zh)
Other versions
CN112250831A (en
Inventor
徐涛
龙绪俭
鲁晓东
杨轩
熊东路
肖增钧
李斌仁
陈林生
许超平
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shenzhen Feiyang Junyan New Material Co ltd
Original Assignee
Shenzhen Feiyang Junyan New Material Co ltd
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.)
Filing date
Publication date
Application filed by Shenzhen Feiyang Junyan New Material Co ltd filed Critical Shenzhen Feiyang Junyan New Material Co ltd
Priority to CN202011083798.2A priority Critical patent/CN112250831B/en
Publication of CN112250831A publication Critical patent/CN112250831A/en
Application granted granted Critical
Publication of CN112250831B publication Critical patent/CN112250831B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C08G18/755Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3225Polyamines
    • C08G18/3228Polyamines acyclic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/44Polycarbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/671Unsaturated compounds having only one group containing active hydrogen
    • C08G18/672Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/14Polyurethanes having carbon-to-carbon unsaturated bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention relates to the technical field of coatings, and particularly relates to UV resin and a preparation method thereof. The UV resin is prepared from the following raw materials in parts by weight: (1) monomer A: the monomer A is one of a compound shown in a formula I and a compound shown in a formula II; (2) monomer B: a five-membered cyclic carbonate; (3) monomer C: a diisocyanate; (4) monomer D: the monomer D is one of a compound shown in a formula III and a compound shown in a formula IV; (5) monomer E: a polycarbonate diol; and (6) a solvent. The UV resin is aliphatic polycarbonate type polyurethane acrylate, has mechanical property adjustability and the characteristics of polyurethane and acrylate, and a cured film has good adhesive force and flexibility, is smooth in appearance and is full; the synthesis method is simple and is beneficial to realizing large-scale production.

Description

UV resin and preparation method thereof
Technical Field
The invention relates to the technical field of coatings, and particularly relates to UV resin and a preparation method thereof.
Background
The ultraviolet curing coating (UV coating) has the advantages of small environmental pollution, high curing speed, energy conservation, good performance of cured products, suitability for high-speed automatic production and the like. Due to the unique technology and application advantages of the UV coating, the UV coating is rapidly and widely applied to various industries and fields of electronic products, mechanical manufacturing, metal corrosion prevention and the like, and is known as a brand new environment-friendly new material. The urethane acrylate is one of UV curing resin oligomers, has the characteristics of both polyurethane and acrylate, and is mainly synthesized from polyol, polyisocyanate and hydroxyl-containing acrylate. Compared with the traditional polyurethane such as polyester polyurethane and polyether polyurethane, the aliphatic polycarbonate polyurethane has better water resistance, aging resistance and flexibility.
As UV cured products evolve into the fields of plastics, metals, ceramics, glass, etc., the inherent drawbacks of some UV coatings are increasingly manifested. Among them, the most important problem in the UV coating industry is the low mechanical properties of the coating after film formation, which is a bottleneck that prevents the UV coating from continuing to develop.
The five-membered ring carbonate is a cheap raw material, is mainly used in the battery industry, and is paid attention to the research work of taking the five-membered ring carbonate as a high polymer material synthetic raw material in order to expand the application range.
Disclosure of Invention
In order to solve the above technical problems, a first aspect of the present invention provides a UV resin, which is prepared from the following raw materials:
(1) Monomer A: the monomer A is one of a compound shown in a formula I and a compound shown in a formula II;
Figure BDA0002719637370000011
wherein n and p are natural numbers;
(2) A monomer B: five-membered cyclic carbonates;
(3) A monomer C: a diisocyanate;
(4) A monomer D: the monomer D is one of a compound shown in a formula III and a compound shown in a formula IV;
Figure BDA0002719637370000021
(5) A monomer E: a polycarbonate diol;
(6) A solvent.
In a preferable technical scheme of the invention, in the compound shown in the formula I, n is 1-150; in the compound shown in the formula II, p is 1-30.
As a preferable technical scheme of the invention, in the compound shown in the formula III, R 2 、R 3 Respectively selecting one of structures shown in formula V and formula VI;
Figure BDA0002719637370000022
as a preferable technical scheme of the invention, in the structure shown in the formula V, R 5 Is one of a structure shown in a formula VII and a structure shown in a formula VIII;
Figure BDA0002719637370000023
wherein m and t are natural numbers.
As a preferable technical scheme, in the structure shown in the formula VI, R 6 Is one of a structure shown in a formula IX and a structure shown in a formula X;
Figure BDA0002719637370000024
wherein r and q are natural numbers.
In a preferred embodiment of the present invention, the polycarbonate diol has a number average molecular weight of 500 to 3000.
The second aspect of the present invention provides a method for preparing the UV resin, comprising the steps of:
(1) Mixing the monomer A, the monomer B and a solvent, reacting for 10-15h at 40-60 ℃, and removing the solvent to obtain an intermediate M;
(2) Under the protection of inert gas, controlling the temperature to be 50-70 ℃, mixing the intermediate M and polycarbonate diol, adding the mixture into the monomer C, reacting for 3-6h, and cooling to obtain an intermediate N;
(3) And (3) under the protection of inert gas, controlling the temperature to be 50-70 ℃, adding the intermediate N into the monomer D, stopping the reaction when the-NCO value is 0, and cooling to obtain the compound.
As a preferred technical solution of the present invention, the molar ratio of the monomer a to the monomer B is 1: (1-5); the molar ratio of the intermediate M to the polycarbonate diol is 1: (1-15).
As a preferable technical scheme of the invention, the dosage of the monomer C is 1 to 5 times of the total molar quantity of the intermediate M and the polycarbonate diol; the molar ratio of the monomer C to the monomer D is 1: (1-5).
The third aspect of the invention provides the application of the UV resin, and the UV resin can be applied to the coating of plastic products, wooden products, metal products, ceramic products and glass products.
Advantageous effects
Compared with the prior art, the UV resin provided by the invention has the following advantages:
1. the UV resin is aliphatic polycarbonate urethane acrylate, has mechanical property adjustability, and can adjust and control the mechanical properties of a cured film, such as elongation at break, tensile strength and the like, by changing the molar ratio and the structure of an intermediate M and polycarbonate diol in raw materials for synthesizing the UV resin.
2. The UV resin has the characteristics of polyurethane and acrylate, and a cured film of the UV resin has good adhesive force and flexibility, is smooth in appearance and is full; the synthesis method is simple and is beneficial to realizing large-scale production.
Detailed Description
The technical features of the technical solutions provided by the present invention will be further clearly and completely described below with reference to the specific embodiments, and it should be apparent that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
It will be understood by those skilled in the art that, unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the prior art and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
The words "preferred", "preferably", "more preferred", and the like, in the context of this invention, refer to embodiments of the invention that may, in some instances, provide certain benefits. However, other embodiments may be preferred, under the same or other circumstances. Furthermore, the recitation of one or more preferred embodiments does not imply that other embodiments are not useful, nor is it intended to exclude other embodiments from the scope of the invention.
In order to solve the above technical problems, a first aspect of the present invention provides a UV resin, which is prepared from the following raw materials:
(1) Monomer A: the monomer A is one of a compound shown in a formula I and a compound shown in a formula II;
Figure BDA0002719637370000041
wherein n and p are natural numbers;
(2) A monomer B: five-membered cyclic carbonates;
(3) A monomer C: a diisocyanate;
(4) A monomer D: the monomer D is one of a compound shown in a formula III and a compound shown in a formula IV;
Figure BDA0002719637370000042
(5) A monomer E: a polycarbonate diol;
(6) A solvent.
Monomer A
In the invention, the monomer A is one of a compound shown in a formula I and a compound shown in a formula II;
Figure BDA0002719637370000043
wherein, n and p are natural numbers.
In a preferred embodiment, in the compounds of formula I, n is 1 to 150; in the compound shown in the formula II, p is 1-30.
In a preferred embodiment, in the compounds of formula I, R is 1 One selected from hydrogen and alkyl.
The alkyl group is not particularly limited, and methyl, ethyl and the like can be mentioned.
The inventor believes that in the compound of formula I, n is 1 to 150; in the compound shown in the formula II, p is 1-30; with the increase of the chain length of the monomer A, the mechanical property of the prepared UV resin after curing tends to be improved and then reduced, and when the chain length of the monomer A exceeds a certain length (n is more than 150 or p is more than 30), the mechanical property of the UV resin after curing is obviously reduced. The inventors considered that the reason is probably that the longer the chain length of the monomer A, the lower the content of hard segment units and the lower the mechanical properties.
Monomer B
In the invention, the monomer B is five-membered cyclic carbonate.
The five-membered cyclic carbonate is not particularly limited, and is commercially available and suitable for use in the present invention.
The inventor finds that the introduction of the cyclic carbonate enables the prepared intermediate M to contain beta hydroxyl and to easily react with isocyanate, on one hand, the cheap five-membered cyclic carbonate compound can obviously reduce the cost, on the other hand, the intermediate M generated by the reaction of amine and cyclic carbonate is matched with polycarbonate diol to synthesize the UV resin, the mechanical property of the UV resin is better than that of the traditional UV resin, and no auxiliary agent is needed in the reaction.
Monomer C
In the invention, the monomer C is diisocyanate.
The diisocyanate is not particularly limited, and is commercially available and suitable for use in the present invention.
In a preferred embodiment, mention may be made of the diisocyanates
Figure BDA0002719637370000051
Figure BDA0002719637370000052
Figure BDA0002719637370000053
And the like.
The inventors have found that only when a diisocyanate is used, the reaction is more controlled and an intermediate N blocked by-NCO groups is obtained, which further bridges structure D to form a UV resin; particularly, isophorone diisocyanate containing three methyl groups is adopted, the compatibility with the whole reaction system is good, and two-NCO groups with larger activity difference are beneficial to synthesis of a prepolymer.
Monomer D
In the invention, the monomer D is one of a compound shown in a formula III and a compound shown in a formula IV;
Figure BDA0002719637370000061
in a preferred embodiment, in the compound of formula III, R 2 、R 3 Respectively selecting one of structures shown in formula V and formula VI;
Figure BDA0002719637370000062
in the structure shown in the formula V, R is 4 Is one of hydrogen and alkyl.
The alkyl group is not particularly limited, and methyl, ethyl and the like can be mentioned.
In the structure shown in the formula V, R 5 Is one of a structure shown in a formula VII and a structure shown in a formula VIII;
Figure BDA0002719637370000063
wherein m and t are natural numbers.
In a preferred embodiment, the structure of formula VII is shown wherein m is from 2 to 20.
In a preferred embodiment, in the structure of formula VIII, t is from 1 to 30.
In a preferred embodiment, in the structure of formula VIII, R 7 Is one of hydrogen and alkyl.
In the structure shown in the formula VI, R in the structure 6 Is one of a structure shown in a formula IX and a structure shown in a formula X;
Figure BDA0002719637370000064
wherein r and q are natural numbers.
In a preferred embodiment, in the structure of formula X, R 8 Is one of hydrogen and alkyl.
In the compound shown in the formula IV, R is 9 Is hydrogen or alkyl; r 10 Is hydrogen or alkyl; r 11 Is hydrogen or alkyl.
Monomer E
In the present invention, the monomer E is a polycarbonate diol.
In a preferred embodiment, the polycarbonate diol has a number average molecular weight of 500 to 3000.
The inventors have found that the larger the number average molecular weight of the polycarbonate diol in the system, the lower the tensile strength after film formation of the resin obtained and the lower the hardness; the smaller the number average molecular weight of the polycarbonate diol, the lower the elongation at break after film formation of the resulting resin. The inventor unexpectedly finds that the comprehensive mechanical properties of the prepared resin are optimal only when polycarbonate diol with the molecular weight of 500-3000 is adopted, and particularly, after the polycarbonate diol is compounded with a compound shown in a formula I with n being 1-150 and an intermediate M prepared from five-membered cyclic carbonate, the resin forms a hard segment unit in a resin structure, so that the mechanical properties of the resin are remarkably improved.
Solvent(s)
In the present invention, the solvent is not particularly limited, and ethanol, methanol, acetone, methylene chloride and the like can be mentioned.
The second aspect of the present invention provides a method for preparing the UV resin, comprising the steps of:
(1) Mixing the monomer A, the monomer B and a solvent, reacting for 10-15h at 40-60 ℃, and evaporating to remove the solvent to obtain an intermediate M;
(2) Under the protection of inert gas, controlling the temperature to be 50-70 ℃, mixing the intermediate M with polycarbonate diol, adding the mixture into the monomer C, reacting for 3-6h, and cooling to obtain an intermediate N;
(3) And (3) under the protection of inert gas, controlling the temperature to be 50-70 ℃, adding the intermediate N into the monomer D, stopping the reaction when the-NCO value is 0, and cooling to obtain the compound.
In a preferred embodiment, the molar ratio of monomer a to monomer B is 1: (1-5); the molar ratio of the intermediate M to the polycarbonate diol is 1: (1-15).
The inventor finds in the experimental process that the dosage of the monomer C in the system cannot be lower than that of the intermediate M, and if the dosage of the monomer C is lower than that of the intermediate M, the intermediate M cannot completely react, the amount of the resin hard segment structure is reduced, and the mechanical property of the resin is reduced; in order to ensure the mechanical property of the resin, the dosage of the monomer C cannot be lower than that of the intermediate M, and meanwhile, the excessive monomer C can also effectively inhibit the gelation phenomenon in the reaction process, so that the reaction can be carried out more smoothly.
In a preferred embodiment, the monomer C is used in an amount of 1 to 5 times the total molar amount of the intermediate M and the polycarbonate diol; the molar ratio of the monomer C to the monomer D is 1: (1-5).
The third aspect of the invention provides the application of the UV resin, and the UV resin can be applied to the coating of plastic products, wooden products, metal products, ceramic products and glass products.
The present invention will be specifically described below by way of examples. It is to be noted that the following examples are given solely for the purpose of illustration and are not to be construed as limitations on the scope of the invention, as many insubstantial modifications and variations of the invention described above will now occur to those skilled in the art.
In addition, the starting materials used are all commercially available, unless otherwise specified.
Examples
Example 1
Embodiment 1 provides a UV resin, and a method for preparing the UV resin, comprising the steps of:
(1) Weighing 230g of polyetheramine D230 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 1
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 14.5g of intermediate M is added 1 Mixing with 600g of polycarbonate diol (Mn = 2000), slowly adding into 148g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.67 percent), and cooling to obtain an intermediate N 1
(3) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 571.8g of intermediate N is added 1 Slowly adding the mixture into 57.8g of hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
Example 2
Embodiment 2 provides a UV resin, and a method for preparing the UV resin, including the steps of:
(1) Weighing 230g of polyetheramine D230 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 2
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 14.5g of intermediate M is added 2 And 333.3g of polycarbonate diol (Mn = 2000), slowly adding the mixture into 148g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.85 percent), and cooling to obtain an intermediate N 2
(3) Under the protection of inert gas, temperature is controlled at 60 ℃, and 327.5g of intermediate N is added 2 Slowly adding into 34.8g hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
Example 3
Embodiment 3 provides a method for preparing a UV resin, comprising the steps of:
(1) Weighing 230g of polyetheramine D230 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 3
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 14.5g of intermediate M is added 3 Mixing with 200g of polycarbonate diol (Mn = 2000), slowly adding 59.2g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (4.1 percent), and cooling to obtain an intermediate N 3
(3) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 205.2g of intermediate N is added 3 Slowly adding the mixture into 23.2g of hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
Example 4
Embodiment 4 provides a method for preparing a UV resin, comprising the steps of:
(1) Weighing 400g of polyetheramine D400 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 4
(2) Under the protection of inert gas, control20.1g of intermediate M are added at 60 ℃ to 4 Mixing with 600g of polycarbonate diol (Mn = 2000), slowly adding into 148g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.64%), cooling to obtain an intermediate N 4
(3) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 576.1g of intermediate N is added 4 Slowly adding the mixture into 57.8g of hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
Example 5
Embodiment 5 provides a method for preparing a UV resin, comprising the steps of:
(1) Weighing 400g of polyetheramine D400 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 5
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 20.1g of intermediate M is added 5 And 333.3g of polycarbonate diol (Mn = 2000), slowly adding the mixture into 88.8g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.8 percent), and cooling to obtain an intermediate N 5
(3) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 331.7g of intermediate N is added 5 Slowly adding into 34.8g hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
Example 6
Embodiment 6 provides a method of preparing a UV resin, comprising the steps of:
(1) Weighing 400g of polyetheramine D400 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 6
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 20.1g of intermediate M is added 6 Mixing with 200g of polycarbonate diol (Mn = 2000), slowly adding 59.2g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (4 percent), and cooling to obtain an intermediate N 6
(3) Under the protection of inert gas, the temperature is controlled at 60 ℃, 209.5g of intermediate N is added 6 Slowly adding the mixture into 23.2g of hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
Example 7
Embodiment 7 provides a UV resin, a method of making the UV resin, comprising the steps of:
(1) Weighing 1000g of polyetheramine D2000, 200g of D400 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 7
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 46.8g of intermediate M is added 7 Mixing with 600g of polycarbonate diol (Mn = 2000), slowly adding into 148g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.52 percent), and cooling to obtain an intermediate N 7
(3) 596.1g of intermediate N is added under the protection of inert gas and the temperature is controlled at 60 DEG 7 Slowly adding 52.3g of hydroxyethyl acrylate and 32.9g of ethanolamine modified acrylate to react, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
The synthesis method of the ethanolamine modified acrylate comprises the following steps: under the protection of dark place, adding 592.6g of trimethylolpropane triacrylate and 600.6g of tripropylene glycol diacrylate into a reaction bottle, heating to 50 ℃, slowly dripping 122g of ethanolamine for reaction, stopping the reaction after no raw material peak is detected by chromatography, and cooling to obtain the product.
Example 8
Embodiment 8 provides a method of preparing a UV resin, comprising the steps of:
(1) Weighing 1000g of polyetheramine D2000, 200g of D400 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 8
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 46.8g of intermediate M is added 8 And 333.3g of polycarbonate diol (Mn = 2000)) Mixing, slowly adding 88.8g of isophorone diisocyanate to react, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.58 percent), and cooling to obtain an intermediate N 8
(3) Under the protection of inert gas, temperature is controlled at 60 ℃, and 351.7g of intermediate N are added 8 Slowly adding 31.4g of hydroxyethyl acrylate and 19.7g of ethanolamine modified acrylate to react, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
The synthesis method of the ethanolamine modified acrylate comprises the following steps: under the protection of dark place, adding 592.6g of trimethylolpropane triacrylate and 600.6g of tripropylene glycol diacrylate into a reaction bottle, heating to 50 ℃, slowly dripping 122g of ethanolamine for reaction, stopping the reaction after no raw material peak is detected by chromatography, and cooling to obtain the product.
Example 9
Embodiment 9 provides a method of preparing a UV resin, comprising the steps of:
(1) Weighing 1000g of polyetheramine D2000, 200g of D400 and 204g of propylene carbonate, adding the materials into a reaction bottle, heating to 50 ℃, reacting for 10 hours, stopping the reaction, cooling, removing the solvent to obtain an intermediate M 9
(2) Under the protection of inert gas, the temperature is controlled at 60 ℃, and 46.8g of intermediate M is added 9 Mixing with 200g of polycarbonate diol (Mn = 2000), slowly adding 59.2g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.66 percent), and cooling to obtain an intermediate N 9
(3) Under the protection of inert gas, the temperature is controlled at 60 ℃, 229.5g of intermediate N are added 9 Slowly adding 20.9g of hydroxyethyl acrylate and 13.2g of ethanolamine modified acrylate to react, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
The synthesis method of the ethanolamine modified acrylate comprises the following steps: under the protection of dark place, adding 592.6g of trimethylolpropane triacrylate and 600.6g of tripropylene glycol diacrylate into a reaction bottle, heating to 50 ℃, slowly dripping 122g of ethanolamine for reaction, stopping the reaction after no raw material peak is detected by chromatography, and cooling to obtain the product.
Example 10
Embodiment 10 provides a method of preparing a UV resin, comprising the steps of:
(1) Under the protection of inert gas, controlling the temperature to be 60 ℃, slowly adding 200g of polycarbonate diol (Mn = 2000) into 44.4g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.43 percent), and cooling to obtain an intermediate 1;
(2) And (3) under the protection of inert gas, controlling the temperature to be 60 ℃, slowly adding 100g of the intermediate 1 into 9.5g of hydroxyethyl acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the compound.
Example 11
Embodiment 11 provides a UV resin, a method of making the UV resin, comprising the steps of:
(1) Under the protection of inert gas, controlling the temperature to be 60 ℃, slowly adding 200g of polycarbonate diol (Mn = 2000) into 44.4g of isophorone diisocyanate for reaction, stopping the reaction when the-NCO value reaches the theoretical-NCO value (3.43%), and cooling to obtain an intermediate 2;
(2) And (3) under the protection of inert gas, controlling the temperature to be 60 ℃, slowly adding 122.2g of the intermediate 2 into 10.5g of hydroxyethyl acrylate and 6.6g of ethanolamine modified acrylate for reaction, stopping the reaction when the-NCO value is 0, and cooling to obtain the product.
In the above embodiments, the polyetheramines D230, D400, and D2000 are all purchased from south china stephani technologies ltd; isophorone diisocyanate is purchased from the German winning industry group; polycarbonate diol purchased from Asahi chemical Co., ltd; ethanolamine, hydroxyethyl acrylate were purchased from Shanghai Aladdin Biotechnology, inc.; trimethylolpropane triacrylate and tripropylene glycol diacrylate are purchased from Yangxing specialty materials, inc.
Performance test
Respectively weighing the UV resin prepared in the embodiment, adding 2wt% of initiator, 15wt% of butyl acetate and 15wt% of reactive diluent, uniformly stirring, respectively coating on a PC-ABS plate, drying in an oven at 60 ℃ to constant weight, taking out, cooling, and curing by a UV machine to obtain a coating film with the thickness of 15 +/-2 micrometers.
And (3) performing performance characterization on the cured coating film:
1. adhesion force: testing according to the national standard GB/T9286;
2. hardness: testing according to the national standard GB/T6739;
3. flexibility: testing according to the national standard GB/T1731;
4. tensile properties (elongation at break and tensile strength): tested according to the national standard GB/T1040.1-2006.
The test results are shown in table 1.
TABLE 1 Performance test results of UV resins prepared in examples
Figure BDA0002719637370000121
Figure BDA0002719637370000131
The foregoing examples are merely illustrative and serve to explain some of the features of the method of the present invention. The appended claims are intended to claim as broad a scope as is contemplated, and the examples presented herein are merely illustrative of selected implementations in accordance with all possible combinations of examples. Accordingly, it is applicants' intention that the appended claims are not to be limited by the choice of examples illustrating features of the invention. Also, where numerical ranges are used in the claims, subranges therein are included, and variations in these ranges are also to be construed as possible being covered by the appended claims.

Claims (2)

1. The UV resin is characterized in that raw materials for preparing the UV resin comprise the following components:
(1) Monomer A: the monomer A is polyether amine D230 or polyether amine D400;
(2) A monomer B: the monomer B is propylene carbonate;
(3) A monomer C: the monomer C is isophorone diisocyanate;
(4) A monomer D: the monomer D is hydroxyethyl acrylate;
(5) A monomer E: the monomer E is polycarbonate diol, and the number average molecular weight of the polycarbonate diol is 2000;
(6) A solvent;
the preparation method of the UV resin comprises the following steps:
(1) Mixing the monomer A, the monomer B and a solvent, reacting for 10-15h at 40-60 ℃, and removing the solvent to obtain an intermediate M;
(2) Under the protection of inert gas, controlling the temperature to be 50-70 ℃, mixing the intermediate M and polycarbonate diol, adding the mixture into the monomer C, reacting for 3-6h, and cooling to obtain an intermediate N;
(3) Under the protection of inert gas, controlling the temperature to be 50-70 ℃, adding the intermediate N into the monomer D, stopping the reaction when the-NCO value is 0, and cooling to obtain the intermediate;
the using amount of the monomer C is 1-5 times of the total molar amount of the intermediate M and the polycarbonate diol; the molar ratio of the monomer C to the monomer D is 1: (1-5);
the molar ratio of the monomer A to the monomer B is 1: (1-5); the molar ratio of the intermediate M to the polycarbonate diol is 1: (1-15).
2. Use of the UV resin according to claim 1 for finishing of plastic, wood, metal, ceramic, glass products.
CN202011083798.2A 2020-10-12 2020-10-12 UV resin and preparation method thereof Active CN112250831B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202011083798.2A CN112250831B (en) 2020-10-12 2020-10-12 UV resin and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202011083798.2A CN112250831B (en) 2020-10-12 2020-10-12 UV resin and preparation method thereof

Publications (2)

Publication Number Publication Date
CN112250831A CN112250831A (en) 2021-01-22
CN112250831B true CN112250831B (en) 2022-11-25

Family

ID=74241798

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202011083798.2A Active CN112250831B (en) 2020-10-12 2020-10-12 UV resin and preparation method thereof

Country Status (1)

Country Link
CN (1) CN112250831B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115785431A (en) * 2022-11-23 2023-03-14 杭州普力材料科技有限公司 Polyether polyol containing carbamate structure and synthesis method and application thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006188589A (en) * 2005-01-05 2006-07-20 Arakawa Chem Ind Co Ltd Active energy ray-curable resin composition and cured film obtained from the composition
CN102190789A (en) * 2011-03-23 2011-09-21 安庆飞凯高分子材料有限公司 Preparation method of polyurethane acrylate resin
CN113881009A (en) * 2021-10-28 2022-01-04 青岛卓英社科技股份有限公司 High-density microporous polyurethane foam and preparation method thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3862021A (en) * 1972-02-17 1975-01-21 Asahi Chemical Ind Polymerizable compositions and laminated articles bonded
JP2007291157A (en) * 2006-04-21 2007-11-08 Kansai Paint Co Ltd Aqueous resin composition and paint composition containing the same
JP5231781B2 (en) * 2007-10-25 2013-07-10 関西ペイント株式会社 Aqueous resin composition and aqueous coating composition containing the same
TWI422607B (en) * 2011-06-29 2014-01-11 Univ Tamkang Functional polyurethane prepolymer, method of preparing polyurethane by using the same, and application method thereof
CN102993397B (en) * 2012-09-13 2014-05-28 太原理工大学 Method for preparing transparent degradable polyurethane
CN104995224B (en) * 2013-01-07 2017-09-01 宇部兴产株式会社 aqueous resin dispersion and its use
CN105801811B (en) * 2014-12-29 2018-03-16 乐凯华光印刷科技有限公司 Photopolymerization urethane acrylate and preparation method thereof
CN105523949A (en) * 2016-01-15 2016-04-27 中国海洋石油总公司 Method for preparing triethanolamine acrylate compound
CN106749942B (en) * 2016-12-15 2019-03-12 深圳飞扬兴业科技有限公司 A kind of 3D printing ultraviolet photocureable material and preparation method thereof
CN107163807A (en) * 2017-04-27 2017-09-15 河北晨阳工贸集团有限公司 The high weather resistant water-thinned acrylic polyurethane finish paint of automatically cleaning and preparation method
CN107177035B (en) * 2017-07-20 2019-10-15 广东工业大学 A kind of base polyurethane prepolymer for use as and preparation method thereof and ultraviolet curing urethane performed polymer composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006188589A (en) * 2005-01-05 2006-07-20 Arakawa Chem Ind Co Ltd Active energy ray-curable resin composition and cured film obtained from the composition
CN102190789A (en) * 2011-03-23 2011-09-21 安庆飞凯高分子材料有限公司 Preparation method of polyurethane acrylate resin
CN113881009A (en) * 2021-10-28 2022-01-04 青岛卓英社科技股份有限公司 High-density microporous polyurethane foam and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
非异氰酸酯聚氨酯的微波合成;丁燕玲等;《广东化工》;20111025(第10期);11-14 *

Also Published As

Publication number Publication date
CN112250831A (en) 2021-01-22

Similar Documents

Publication Publication Date Title
EP2838954B1 (en) Adhesive compositions and methods
CA2064986C (en) High performance polyurethane coating compositions and processes for making same
CN112048051B (en) Polyurethane acrylate resin and preparation method thereof
TWI338023B (en) Multi-component, waterborne coating compositions, related coatings and methods
US3830785A (en) Thermosetting polyurethane coatings based on blocked cyclo-aliphatic diisocyanates
WO2005105857A1 (en) Polyester-polyether hybrid urethane acrylate oligomer for uv curing pressure sensitive adhesives
AU4752000A (en) Composition comprising mercapto-functional compounds
DE2514816A1 (en) POLYESTER RESIN COMPOUND FOR POWDER-SHAPED PAINTS
JP2008501057A (en) Catalyst composition
MXPA96000899A (en) Polyurethane coatings with ultra-basket based on volati organic components
CN108129635B (en) Hydrophobic flame-retardant water-based curing agent and preparation method thereof
CN101274977B (en) Curing agent 1,6- hexamethylene diisocyanate prepolymer and preparation thereof
CA2041060A1 (en) Polyurethane reaction mixtures and coating compositions
CN112250831B (en) UV resin and preparation method thereof
CN110511662A (en) A kind of double-composition polyurethane waterproof paint and preparation method thereof
EP4010389A1 (en) One-component type polyurethane prepolymer composition
CN113544181B (en) Non-aqueous crosslinkable compositions
JP6582515B2 (en) Polyurethane resin and leather adhesive using the composition
JPS6136373A (en) Polyurethane coating composition, its production and method for lowering its viscosity
CA1129144A (en) Stable unsaturated urethane oligomers
KR101131888B1 (en) Paint composition for plastics and method of preparing the same
WO2015038449A1 (en) Coating compositions and methods for their use
JPS584068B2 (en) fast curing paint
CN104356020A (en) Novel acylamino ester as well as synthesis method and application thereof
JPH10101999A (en) Binder composition for coating metallic and mineral substrates and its use

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20221028

Address after: 518100 805, building B, Feiyang science and Technology Innovation Park, No. 8, Longchang Road, district 67, Xingdong community, Xin'an street, Bao'an District, Shenzhen City, Guangdong Province

Applicant after: SHENZHEN FEIYANG JUNYAN NEW MATERIAL CO.,LTD.

Address before: 518000 8th floor, building B, Feiyang Xingye technology plant, Liuxian 2nd Road, Xin'an street, Bao'an District, Shenzhen City, Guangdong Province

Applicant before: SHENZHEN FEIYANG XINGYE TECHNOLOGY CO.,LTD.

GR01 Patent grant
GR01 Patent grant