CN106189802A - A kind of UV solidification solvent-free height saturating non-yellow stain polyurethane minute surface resin and preparation method thereof - Google Patents
A kind of UV solidification solvent-free height saturating non-yellow stain polyurethane minute surface resin and preparation method thereof Download PDFInfo
- Publication number
- CN106189802A CN106189802A CN201610547032.2A CN201610547032A CN106189802A CN 106189802 A CN106189802 A CN 106189802A CN 201610547032 A CN201610547032 A CN 201610547032A CN 106189802 A CN106189802 A CN 106189802A
- Authority
- CN
- China
- Prior art keywords
- minute surface
- polyurethane
- solvent
- surface resin
- free height
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
-
- 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
- C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
- C08G18/4269—Lactones
- C08G18/4277—Caprolactone and/or substituted caprolactone
-
- 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
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06N3/042—Acrylic polymers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2203/00—Macromolecular materials of the coating layers
- D06N2203/04—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2211/00—Specially adapted uses
- D06N2211/12—Decorative or sun protection articles
- D06N2211/28—Artificial leather
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Textile Engineering (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention discloses a kind of UV and solidify solvent-free height saturating non-yellow stain polyurethane minute surface resin, belonging to mirror surface leather technical field, it includes that the component of following mass percent is made: two degree of functionality polyurethane 20.5 40.6%, trifunctional reactive diluent 25.0 35.0%, two functional group's reactive diluent 30.8 47.6%, light trigger 1.0 5.0%, levelling agent 0.1 0.4% and defoamer 0.1 0.4%.A kind of UV solidification solvent-free height saturating non-yellow stain polyurethane minute surface resin of the present invention is entirely free of the environment-friendly polyurethane minute surface resin of any organic solvent, and its physical property exceedes dry method veneer and moisture-curable minute surface, and production efficiency is high, can be with instantaneous solidification molding;The process synthesis of the preparation method of the present invention is a kind of solventfree resin, in process of production without any organic solvent emission, without any organic solvent in the solvent-free mirror surface leather of gained, VOC content is extremely low, use a cutter coating processes without tie layer resins, decrease the technological process of production, reduce production and cost of material, and without any organic solvent emission.
Description
Technical field
The invention belongs to mirror surface leather technical field, be specifically related to a kind of UV and solidify solvent-free height saturating non-yellow stain polyurethane minute surface
Resin and preparation method thereof.
Background technology
Along with the raising day by day of our people's living standard, people are increasingly wider to the demand of consumer goods, therefore high transparency
High performance case and bag, footwear demand are increasing.
Traditional mirror surface leather is mainly prepared by two ways, and one is exactly dry method veneer, solvent-borne type slurry is scratched in
Above mirror surface paper, dry out solvent uses solvent-borne type bed material laminating bass again, and this process uses the poisonous and harmful solvents such as DMF in a large number.Phase
Than with do mirror surface leather, the mirror surface leather planarization of moisture-curable gained and brightness by dry method veneer and to exceed a lot, the highest
The mirror surface leather of end is substantially to be prepared by moisture-curable, but the production process environment of moisture-curable is very severe, and
And extremely inefficient, preparation method is solvent-borne type slurry to add after a large amount of solvent dilution showering to leather surface, stands and makes solvent natural
Volatilization, the solvent of 90% evaporate in air, needs the cool system of room temperature 24 hours, and production process needs dedusting, it is necessary to airtight,
Can not ventilate, operator are injured and huge, simultaneously because whole space is full of inflammable and explosive solvent, therefore dangerous
Also very big, additionally from being to react solidification by isocyanates and water due to moisture-curable product, therefore goods resistance to low temperature is poor,
The product that low temperature complications are required by footwear etc. cannot be done.Therefore in people's growing interest health and today of environmental protection, exploitation one
Solvent-free height without any organic solvent, pollution-free, high efficiency, low energy consumption and physical properties excellent is thoroughly without xanthochromia mirror surface leather tree
Fat is the most meaningful.
Resin is coated in base fabric solidification by UV curing of the prior art, then carries out veneer with water-base resin, tool
There are the features such as curing efficiency height, environmental friendliness, energy consumption are low, but use the method for water-base resin veneer not simply fail to accomplish high lens
Upper leather effect, and add energy consumption and cost.
Summary of the invention
Goal of the invention: it is an object of the invention to provide a kind of UV and solidify solvent-free height saturating non-yellow stain polyurethane minute surface resin
Being entirely free of the environment-friendly polyurethane minute surface resin of any organic solvent, its physical property exceedes dry method veneer and moisture-curable mirror
Face, production efficiency is high, can be with instantaneous solidification molding.It is a further object of the present invention to provide the preparation method of this resin.
Technical scheme: for achieving the above object, the present invention adopts the following technical scheme that
A kind of UV solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, including the component system of following mass percent
Become: two degree of functionality polyurethane 20.5-40.6%, trifunctional reactive diluent 25.0-35.0%, two functional group's reactive diluents
30.8-47.6%, light trigger 1.0-5.0%, levelling agent 0.1-0.4% and defoamer 0.1-0.4%;Wherein, described two
Degree of functionality polyurethane includes that the component of following mass percent is made: polycaprolactone diols 22.8-52.6%, aliphatic isocyanide
Acid esters 26.5-58.5%, catalyst 0.01-0.03%, hydroxy acrylate 15.0-25.0% and polymerization inhibitor 0.3-1.0%.
Described polycaprolactone diols is selected from Capa 2054, Capa 2043, PCL 205, PCL 205U and PCLL
Any one or a few combination in 205AL.
Described aliphatic isocyanates is any one or a few combination in IPDI, H12MDI and HDI.
Described catalyst is selected from TEGOKAT 722, TEGOCAT 716, BICAT 8108, BICAT 8220, Borchi
Any one or a few combination in Kat24, Borchi Kat243 and BicatZ.
Described hydroxy acrylate is selected from 2-(Acryloyloxy)ethanol, Hydroxypropyl acrylate, hydroxyethyl methylacrylate and first
Any one or a few combination in base Hydroxypropyl acrylate.
Described polymerization inhibitor selected from MEHQ, di-t-butyl hydroquinone, 2, in 5-di-tert-butyl hydroquinone
Any one or a few combination.
Described light trigger is Darocur-1173 and/or Irgacure 184.
Described levelling agent selected from BYK-UV3510, BYK-UV3500, TEGO Flow300, TEGO Rad 2200N and
Any one or a few combination in TEGO Rad 2100.
Described trifunctional reactive diluent is ethoxylated trimethylolpropane triacrylate;Two described senses
Group's reactive diluent is in 1,6 hexanediyl esters, neopentylglycol diacrylate and tripropylene glycol diacrylate
Any one or a few combination.
Described defoamer is any one or a few combination in BYK1790, BYK056A and BYK066N.
The method of the UV solidification solvent-free height saturating non-yellow stain polyurethane minute surface resin described in preparation comprises the steps:
1) two degree of functionality polyurethane are prepared
Aliphatic isocyanates is put into reactor, is warmed up to 60-65 DEG C, drip polycaprolactone diols, drip complete
Rear input catalyst, 65-70 DEG C is incubated 2 hours, measures input polymerization inhibitor after nco value is less than 0.2% and is warmed up to 80-85 DEG C of addition
Hydroxy acrylate, adds catalyst after dropping, 80-85 DEG C is incubated 3 hours, after detection NCO is qualified, and cooling packaging;
2) prepare UV and solidify solvent-free height saturating non-yellow stain polyurethane minute surface resin
By two degree of functionality polyurethane, two degree of functionality reactive diluents, three-functionality-degree reactive diluent, levelling agent, defoamer
Mix in proportion, then deaeration, packaging.
Beneficial effect: compared with prior art, a kind of UV of the present invention solidifies solvent-free height saturating non-yellow stain polyurethane minute surface
Resin is by introducing a large amount of acrylic resin with double bond on polyurethane resin molecule segment so that product i.e. has propylene
The penetrating sense of acid has again the pliability of polyurethane, and surface is dry sliding and resistance to low temperature is good, overcomes moisture-curable mirror surface leather low
Temperature flexibility difference cannot be used for the defect in collar territory;Using UV solidification, owing to radical polymerization is very rapid, product coats
Several seconds curing moldings after ultraviolet lighting, its production efficiency far surpasses the method for dry method veneer and moisture-curable, additionally, due to solidification
Rapidly, humidity and dust removing effects to workshop require the lowest;The process synthesis of the preparation method of the present invention is a kind of nothing
Solvent Resin, in process of production without any organic solvent emission, without any organic solvent, VOC in the solvent-free mirror surface leather of gained
Content is extremely low, uses a cutter coating processes without tie layer resins, decreases the technological process of production, reduces production and raw material becomes
This, and without any organic solvent emission.
Detailed description of the invention
Below in conjunction with detailed description of the invention, it is further elucidated with the present invention.
Solvent-free height saturating non-yellow stain polyurethane minute surface resin, first synthesizes two degree of functionality polyurethane, resynthesis minute surface resin.Two
Degree of functionality polyurethane includes the component of following mass percent: polycaprolactone diols 22.8-52.6%, aliphatic isocyanates
26.5-58.5%, catalyst 0.01-0.03%, hydroxy acrylate 15.0-25.0% and polymerization inhibitor 0.3-1.0%.
Minute surface resin includes the component of following mass percent: two degree of functionality polyurethane 20.5-40.6%, trifunctional are lived
Property diluent 25.0-35.0%, two functional group reactive diluent 30.8-47.6%, light trigger 1.0-5.0%, levelling agent
0.1-0.4% and defoamer 0.1-0.4%.
Polycaprolactone diols is in Capa 2054, Capa 2043, PCL 205, PCL 205U and PCLL 205AL
Any one or a few combination.
Aliphatic isocyanates selected from IPDI (isophorone and isocyanates), (hydrogenated diphenyl methane two is different for H12MDI
Cyanate) and HDI (hexamethylene diisocyanate) in any one or a few combination.
Catalyst selected from TEGOKAT 722, TEGOCAT 716, BICAT 8108, BICAT 8220, Borchi Kat24,
Any one or a few combination in Borchi Kat243 and BicatZ.
Hydroxy acrylate is selected from 2-(Acryloyloxy)ethanol, Hydroxypropyl acrylate, hydroxyethyl methylacrylate and metering system
Any one or a few combination in acid hydroxypropyl acrylate.
Polymerization inhibitor selected from MEHQ, di-t-butyl hydroquinone, 2, any one in 5-di-tert-butyl hydroquinone
Kind or several combinations.
Light trigger is Darocur-1173 and/or Irgacure 184.
Levelling agent is selected from BYK-UV3510, BYK-UV3500, TEGO Flow300, TEGO Rad 2200N and TEGO Rad
Any one or a few combination in 2100.
Trifunctional reactive diluent is ethoxylated trimethylolpropane triacrylate (TMPTA).
Two functional group's reactive diluents are selected from 1,6 hexanediyl esters (HDDA), neopentylglycol diacrylate
And any one or a few combination in tripropylene glycol diacrylate (TPGDA) (NPGDA).Defoamer selected from BYK1790,
Any one or a few combination in BYK056A and BYK066N.
A kind of UV solidifies solvent-free height saturating non-yellow stain polyurethane minute surface process for preparing resins, includes following steps:
1) two degree of functionality polyurethane are standby:
Aliphatic isocyanates is put into reactor, is warmed up to 60-65 DEG C, drip polycaprolactone diols, drip complete
Rear input catalyst, 65-70 DEG C be incubated 2 hours, measure NCO (NCO in chemical material) value, qualified after put into inhibition
Agent is warmed up to 80-85 DEG C and adds hydroxy acrylate, adds catalyst after dropping, and 80-85 DEG C is incubated 3 hours, detects NCO
After qualified, cooling packaging;
2) solvent-free minute surface resin-made is standby:
By two degree of functionality polyurethane, two degree of functionality reactive diluents, three-functionality-degree reactive diluent, levelling agent, defoamer
Mix in proportion, then deaeration, packaging;
3), when using, solvent-free minute surface resin is scratched 0.1mm-0.3mm on the plain weave posting face is removed from office, solid by UV light
The solidification of change machine i.e. can get solvent-free height saturating non-yellow stain polyurethane mirror surface leather.
Embodiment 1
Two degree of functionality polyurethane are standby: 301g aliphatic isocyanates IPDI is put into reactor, is warmed up to 60-65 DEG C,
Dropping 516g polycaprolactone diols Capa2054, puts into 0.1g catalyst TEGOKAT 722,65-70 DEG C of guarantor after dropping
Temperature 2 hours, measure nco value, less than 0.5% after put into polymerization inhibitor hydroxyanisol 6g be warmed up to 80-85 DEG C add 184g propylene
Acid hydroxyl ethyl ester, adds 0.2g catalyst TEGOKAT 722 after dropping, 80-85 DEG C is incubated 3 hours, and detection nco value is less than
0.2%, cooling packaging.
Solvent-free minute surface resin-made is standby: by two degree of functionality polyurethane 222g, two degree of functionality reactive diluent neopentyl glycols two
Acrylate (NPGDA) 278g, three-functionality-degree reactive diluent ethoxylated trimethylolpropane triacrylate (TMPTA)
456g, initiator Darocur-1173 40g, levelling agent BYK-UV3500 2g, defoamer BYK066N 2g mix homogeneously, then take off
Bubble, packaging.
Solvent-free minute surface resin scratched 0.1mm-0.3mm on the plain weave posting face is removed from office by gained, solid by UV light
Change machine solidifies.The solvent-free height of gained is the most high without xanthochromia mirror surface leather production efficiency, and without any organic solvent, physical property is complete
Entirely reach mirror surface leather requirement, particularly low temperature flexibility and can reach-10 DEG C, do not rupture for 100,000 times;120 degree of heat-resisting post yellowings of 24h
Grade exceedes level Four;The test of 24h color inhibition exceedes level Four.
Embodiment 2
Two degree of functionality polyurethane are standby: 375g aliphatic isocyanates H12MDI is put into reactor, is warmed up to 60-65
DEG C, drip 425g polycaprolactone diols Capa 2043, after dropping, put into 0.1g catalyst TEGOCAT 716,65-70
DEG C insulation 2 hours, measures nco value and adds less than putting into polymerization inhibitor di-t-butyl hydroquinone 6g after 0.5% and being warmed up to 80-85 DEG C
Entering 200g Hydroxypropyl acrylate, add 0.2g catalyst TEGOCAT 716 after dropping, 80-85 DEG C is incubated 3 hours, detection
Nco value is less than 0.2%, cooling packaging.
Solvent-free minute surface resin-made is standby: by two degree of functionality polyurethane 306g, two degree of functionality reactive diluent neopentyl glycols two
Acrylate (NPGDA) 295g, three-functionality-degree reactive diluent ethoxylated trimethylolpropane triacrylate (TMPTA)
355g, initiator Darocur-1173 40g, levelling agent BYK-UV3510 2g, defoamer BYK1790 2g mix homogeneously, then take off
Bubble, packaging.
Solvent-free minute surface resin scratched 0.1mm-0.3mm on the plain weave posting face is removed from office by gained, solid by UV light
Change machine solidifies.The solvent-free height of gained is the most high without xanthochromia mirror surface leather production efficiency, and without any organic solvent, physical property is complete
Entirely reach mirror surface leather requirement, particularly low temperature flexibility and can reach-10 DEG C, do not rupture for 100,000 times;120 degree of heat-resisting post yellowings of 24h
Grade exceedes level Four;The test of 24h color inhibition exceedes level Four.
Embodiment 3
Two degree of functionality polyurethane are standby: 426g aliphatic isocyanates H12MDI is put into reactor, is warmed up to 60-65
DEG C, drip 342g polycaprolactone diols PCL 205, after dropping, put into 0.1g catalyst BICAT 8108,65-70 DEG C of guarantor
Temperature 2 hours, measures input polymerization inhibitor 6g after nco value is less than 0.5% and is warmed up to 80-85 DEG C of addition 232g hydroxyethyl methacrylate second
Ester, adds 0.2g catalyst BICAT 8108 after dropping, 80-85 DEG C is incubated 3 hours, after detection nco value is less than 0.2%,
Cooling packaging.
Solvent-free minute surface resin-made is standby: by two degree of functionality polyurethane 381g, two degree of functionality reactive diluent tripropylene glycols two
Acrylate (TPGDA) 257g, three-functionality-degree reactive diluent ethoxylated trimethylolpropane triacrylate (TMPTA)
318g, initiator Darocur-1173 4g, levelling agent TEGO Flow300 2g, defoamer BYK056A 2g mix homogeneously, then
Deaeration, packaging.
Solvent-free minute surface resin scratched 0.1mm-0.3mm on the plain weave posting face is removed from office by gained, solid by UV light
Change machine solidifies.The solvent-free height of gained is the most high without xanthochromia mirror surface leather production efficiency, and without any organic solvent, physical property is complete
Entirely reach mirror surface leather requirement, particularly low temperature flexibility and can reach-10 DEG C, do not rupture for 100,000 times;120 degree of heat-resisting post yellowings of 24h
Grade exceedes level Four;The test of 24h color inhibition exceedes level Four.
Claims (11)
1. a UV solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: include following mass percent
Component make: two degree of functionality polyurethane 20.5-40.6%, trifunctional reactive diluent 25.0-35.0%, two functional groups live
Property diluent 30.8-47.6%, light trigger 1.0-5.0%, levelling agent 0.1-0.4% and defoamer 0.1-0.4%;Wherein,
Two described degree of functionality polyurethane include that the component of following mass percent is made: polycaprolactone diols 22.8-52.6%, fat
Fat race isocyanates 26.5-58.5%, catalyst 0.01-0.03%, hydroxy acrylate 15.0-25.0% and polymerization inhibitor 0.3-
1.0%.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Polycaprolactone diols any one in Capa 2054, Capa 2043, PCL 205, PCL 205U and PCLL 205AL
Kind or several combinations.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Aliphatic isocyanates any one or a few combination in IPDI, H12MDI and HDI.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Catalyst selected from TEGOKAT 722, TEGOCAT 716, BICAT 8108, BICAT 8220, Borchi Kat24, Borchi
Any one or a few combination in Kat243 and BicatZ.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Hydroxy acrylate selected from 2-(Acryloyloxy)ethanol, Hydroxypropyl acrylate, hydroxyethyl methylacrylate and methacrylic acid hydroxypropyl
Any one or a few combination in ester.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Polymerization inhibitor selected from MEHQ, di-t-butyl hydroquinone, 2, in 5-di-tert-butyl hydroquinone any one or several
The combination planted.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Light trigger be Darocur-1173 and/or Irgacure 184.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Levelling agent selected from BYK-UV3510, BYK-UV3500, TEGO Flow300, TEGO Rad 2200N and TEGO Rad 2100
In any one or a few combination.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: described
Trifunctional reactive diluent be ethoxylated trimethylolpropane triacrylate;Two described functional group's reactive diluents
Selected from 1, in 6 hexanediyl esters, neopentylglycol diacrylate and tripropylene glycol diacrylate any one or several
The combination planted.
UV the most according to claim 1 solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin, it is characterised in that: institute
The defoamer stated is any one or a few combination in BYK1790, BYK056A and BYK066N.
In 11. preparation claim 1~10, the UV described in any one solidifies solvent-free height saturating non-yellow stain polyurethane minute surface resin
Method comprise the steps:
1) two degree of functionality polyurethane are prepared
Aliphatic isocyanates is put into reactor, is warmed up to 60-65 DEG C, drip polycaprolactone diols, throw after dropping
Entering catalyst, 65-70 DEG C is incubated 2 hours, measures input polymerization inhibitor after nco value is less than 0.2% and is warmed up to 80-85 DEG C of addition hydroxyl
Acrylate, adds catalyst after dropping, 80-85 DEG C is incubated 3 hours, after detection NCO is qualified, and cooling packaging;
2) prepare UV and solidify solvent-free height saturating non-yellow stain polyurethane minute surface resin
By two degree of functionality polyurethane, two degree of functionality reactive diluents, three-functionality-degree reactive diluent, levelling agent, defoamer by than
Example mix homogeneously, then deaeration, packaging.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610547032.2A CN106189802B (en) | 2016-07-13 | 2016-07-13 | A kind of solvent-free high non-yellow stain polyurethane mirror surface resin and preparation method thereof thoroughly of UV solidification |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610547032.2A CN106189802B (en) | 2016-07-13 | 2016-07-13 | A kind of solvent-free high non-yellow stain polyurethane mirror surface resin and preparation method thereof thoroughly of UV solidification |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106189802A true CN106189802A (en) | 2016-12-07 |
CN106189802B CN106189802B (en) | 2018-12-25 |
Family
ID=57477472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610547032.2A Active CN106189802B (en) | 2016-07-13 | 2016-07-13 | A kind of solvent-free high non-yellow stain polyurethane mirror surface resin and preparation method thereof thoroughly of UV solidification |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106189802B (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107160750A (en) * | 2017-04-14 | 2017-09-15 | 安徽宝博合成革有限公司 | A kind of aqueous/solvent-free minute surface Synthetic Leather preparation technology |
CN109440483A (en) * | 2018-09-11 | 2019-03-08 | 东莞市雄林新材料科技股份有限公司 | A kind of high scratch resistance mirror surface super fiber leather and preparation method thereof |
CN110105530A (en) * | 2019-05-10 | 2019-08-09 | 广州回天新材料有限公司 | A kind of UV moisture double cured resin preparation method |
CN110330628A (en) * | 2019-07-10 | 2019-10-15 | 福建元发树脂有限公司 | Non-solvent single-component polyurethane mirror surface resin |
CN111349196A (en) * | 2018-12-21 | 2020-06-30 | 义获嘉伟瓦登特公司 | Composition for producing dental components with fracture toughness by stereolithography |
CN112225868A (en) * | 2020-09-30 | 2021-01-15 | 华南理工大学 | Two-three functionality mixed polyurethane acrylate resin and preparation method thereof |
CN115300400A (en) * | 2021-05-07 | 2022-11-08 | 义获嘉伟瓦登特公司 | Transparent, fracture-tough polymeric resins for the production of dental molded bodies |
US11697696B2 (en) | 2018-12-21 | 2023-07-11 | Ivoclar Vivadent Ag | Compositions for the production of transparent dental parts by means of stereolithography |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101173032A (en) * | 2007-10-15 | 2008-05-07 | 广州市博兴化工科技有限公司 | Large-molecular weight polyurethane acrylic ester and synthesizing method thereof |
CN102604035A (en) * | 2012-03-13 | 2012-07-25 | 广东深展实业有限公司 | Ultraviolet cured two-degree-of-functionality polyurethane acrylic ester base coating resin for vacuum coating |
CN103031105A (en) * | 2012-12-26 | 2013-04-10 | 深圳市锦联科技有限公司 | Ultraviolet curing liquid optical clear adhesive and preparation method thereof |
-
2016
- 2016-07-13 CN CN201610547032.2A patent/CN106189802B/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101173032A (en) * | 2007-10-15 | 2008-05-07 | 广州市博兴化工科技有限公司 | Large-molecular weight polyurethane acrylic ester and synthesizing method thereof |
CN102604035A (en) * | 2012-03-13 | 2012-07-25 | 广东深展实业有限公司 | Ultraviolet cured two-degree-of-functionality polyurethane acrylic ester base coating resin for vacuum coating |
CN103031105A (en) * | 2012-12-26 | 2013-04-10 | 深圳市锦联科技有限公司 | Ultraviolet curing liquid optical clear adhesive and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
李小瑞等: "《皮革化学品》", 31 August 2014 * |
李红强: "《胶粘原理、技术及应用》", 31 January 2014 * |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107160750A (en) * | 2017-04-14 | 2017-09-15 | 安徽宝博合成革有限公司 | A kind of aqueous/solvent-free minute surface Synthetic Leather preparation technology |
CN109440483A (en) * | 2018-09-11 | 2019-03-08 | 东莞市雄林新材料科技股份有限公司 | A kind of high scratch resistance mirror surface super fiber leather and preparation method thereof |
CN111349196A (en) * | 2018-12-21 | 2020-06-30 | 义获嘉伟瓦登特公司 | Composition for producing dental components with fracture toughness by stereolithography |
US11697696B2 (en) | 2018-12-21 | 2023-07-11 | Ivoclar Vivadent Ag | Compositions for the production of transparent dental parts by means of stereolithography |
US11753537B2 (en) | 2018-12-21 | 2023-09-12 | Ivoclar Vivadent Ag | Compositions for the production of fracture-tough dental parts by means of stereolithography |
CN110105530A (en) * | 2019-05-10 | 2019-08-09 | 广州回天新材料有限公司 | A kind of UV moisture double cured resin preparation method |
CN110330628A (en) * | 2019-07-10 | 2019-10-15 | 福建元发树脂有限公司 | Non-solvent single-component polyurethane mirror surface resin |
CN112225868A (en) * | 2020-09-30 | 2021-01-15 | 华南理工大学 | Two-three functionality mixed polyurethane acrylate resin and preparation method thereof |
CN115300400A (en) * | 2021-05-07 | 2022-11-08 | 义获嘉伟瓦登特公司 | Transparent, fracture-tough polymeric resins for the production of dental molded bodies |
Also Published As
Publication number | Publication date |
---|---|
CN106189802B (en) | 2018-12-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106189802A (en) | A kind of UV solidification solvent-free height saturating non-yellow stain polyurethane minute surface resin and preparation method thereof | |
CN103214653B (en) | Resinize and its preparation method and application in a kind of ultraviolet light solidfication water polyurethane face | |
CN103232585B (en) | A kind of preparation method of polyfunctionality polyurethane acrylic ester water UV resin | |
CN103274967B (en) | Tri-functional polyurethane acrylate, and preparation method and application thereof | |
CN104559741B (en) | UV (ultraviolet) finishing varnish for laser roller coating | |
CN103224603B (en) | Urethane acrylate with six functionalities as well as preparation method and application thereof | |
KR20130140537A (en) | Radical-curable hot-melt urethane resin composition and moldings for optical use | |
CN103589324B (en) | The anti-scratch matte varnish of a kind of UV | |
CN106854432A (en) | A kind of radiation solidified aqueous coating resin and preparation method thereof | |
CN107129788B (en) | UV (ultraviolet) curing pressure-sensitive adhesive | |
CN111732887A (en) | Solvent-based spray photocuring antibacterial coating and preparation method and application thereof | |
CN103242508B (en) | A kind of 4 functionality urethane acrylates and its preparation method and application | |
CN102977748A (en) | UV furniture spray-coating gloss topcoat without volatile organic solvent | |
CN102816509B (en) | High workability polyurethane coating | |
CN103214649B (en) | 9-functionality-degree polyurethane acrylate as well as preparation method and application thereof | |
CN103193953B (en) | Urethane acrylate with functionality of 12 as well as preparation method and application thereof | |
US11254782B2 (en) | Biomaterial-based UV coating composition | |
CN105295817B (en) | A kind of preparation method of high-solid content water-based polyurethane adhesive | |
CN109868091A (en) | A kind of water vacuum plastics-absorption glue and preparation method thereof | |
JP2012017404A (en) | Photocurable resin composition and photocurable coating agent using the same | |
CN106634457A (en) | UV (ultraviolet) glossy finish paint capable of being used for spray coating and laser roller coating | |
CN105542121B (en) | UV-cured polyurethane acrylate and preparation method thereof | |
CN104448172A (en) | Photosensitive waterborne acrylic acid-polyurethane dispersion and coating thereof | |
CN105820063B (en) | A kind of 4 degree of functionality urethane acrylates based on anhydrous citric acid and its preparation method and application | |
CN103214652B (en) | Ultraviolet cured waterborne polyurethane acrylate vacuum coating base-coating resin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |