CN102436145A - Stereo lithography rapid prototyping photosensitive resin and preparation method thereof - Google Patents

Stereo lithography rapid prototyping photosensitive resin and preparation method thereof Download PDF

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Publication number
CN102436145A
CN102436145A CN2011102554018A CN201110255401A CN102436145A CN 102436145 A CN102436145 A CN 102436145A CN 2011102554018 A CN2011102554018 A CN 2011102554018A CN 201110255401 A CN201110255401 A CN 201110255401A CN 102436145 A CN102436145 A CN 102436145A
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photosensitive resin
rapid shaping
stereolithography rapid
resin according
shaping photosensitive
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CN102436145B (en
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黄笔武
陈新平
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Nanchang University
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Nanchang University
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Abstract

The invention relates to a stereo lithography rapid prototyping photosensitive resin which is characterized by comprising the following raw materials according to the mass ratio: 5-30% of ethylene glycol diglycidyl ether diacrylate, 5-75% of epoxy resin, 5-55% of oxacyclobutane compound, 1-12% of cationic initiator, 5-50% of acrylic ester prepolymer and 1-10% of radical photopolymerization initiator. A preparation method of the stereo lithography rapid prototyping photosensitive resin comprises the steps of: mixing the raw material components according to the mass ratio; and then, heating and stirring, namely, stirring for 5-120 minutes at the temperature of 20-80 DEG C, and leading the obtained mixture to become transparent faint yellow uniform liquid. The photosensitive resin is low in irritation and less in volatile matter, and has good light sensitivity, wherein the critical exposure Ec is less than 16.5mJ/ cm<2>; a molded part is high in accuracy and has the warpage factors CF (6) within the range of 0.01 to -0.01 and CF (11) within the range of 0.03 to -0.03; and parts with any complicated shapes and high accuracy can be directly manufactured, and the manufacturing cost is very low.

Description

A kind of stereolithography rapid shaping photosensitive resin and preparation method
Technical field
The invention belongs to rapid shaping and make the field, relate to rapid shaping photosensitive resin and preparation.
Background technology
Since U.S. 3D Systems company in 1988 releases stereolithography rapid shaping machine the earliest; This make-up machine with the complicacy that can automatically produce various job operations and be difficult to make the three-dimensional shape object, in processing technique field, have epoch making significance.It is to be raw material with the liquid photosensitive resin; Under the control of computing machine; Ultra-Violet Laser is pressed each layering cross-section data liquid towards photosensitive resin surface point by point scanning of part, makes by the thin resin layer of scanning area to produce photopolymerization reaction and solidify a thin layer of formation part; After one deck curing finished, worktable descended, and applied the new liquid resin of one deck again so that descend one deck scanning to solidify at the resin surface that originally was cured; New one deck that solidifies is bonded in again on preceding one deck securely; So repeat, finish up to the whole part making.In the stereolithography quick shaping process, photosensitive resin is its basis, and its composition and ultraviolet-curing paint, printing ink are formed somewhat identical, promptly are made up of light trigger, prepolymer, thinning agent and little additive.But the stereolithography quick shaping process has specific (special) requirements to its photosensitive resin, and it requires photosensitive resin to have following characteristics: (1) viscosity is low, and the low-viscosity resin helps the very fast levelling of resin ability in the moulding; (2) pungency is little few with volatile matter, helps operator's health and does not cause environmental pollution; (3) cure shrinkage is little, and light-cured resin can produce internal stress and shrinks being converted into by liquid state in the solid-state process, and this contraction can cause the distortion of original paper in manufacturing process, warpage, cracking etc., and the precision of forming part is reduced; (4) swelling is little, and the swelling of hygrometric state profiled member in the resin of liquid state can cause accessory size bigger than normal; (5) susceptibility to light is high, and promptly the scope of institute's absorbing wavelength is narrow, to improve the making precision of part; (6) good with the light source matching, to make full use of luminous energy, improve and solidify yield; (7) resin bonding property is strong, does not produce splitting to guarantee the back solidification process; (8) solidification rate is fast, to enhance productivity; (9) bin stability is good, and general storage life is Ying Yinian at least; (10) cost is low, is beneficial to commercialization.Because the required photosensitive resin of stereolithography rapid shaping needs to satisfy above these characteristics simultaneously, cause its photosensitive resin research and development to have certain degree of difficulty.
Now, the photosensitive resin that is applied to the stereolithography rapid shaping abroad mainly is that free radical-cation type mixes type photosensitive resin, and the characteristics of this photosensitive resin are that prepolymer and thinning agent are main with epoxy resin, and acrylic ester is auxilliary.This photosensitive resin concentrated the acrylic ester curing rate fast with the little advantage of epoxy resin cure contraction, making it photosensitive resin, both to have had photosensitivity good, has the high characteristics of profiled member precision again.For example, the photosensitive resin of the photosensitive resin of U.S. DSM Somos company and Huntsman company just belongs to free radical-cation type and mixes type photosensitive resin.Now, this two company is that per kilogram is sold to China up to 1500 yuans with the selling price, and is monopolizing the market of China's stereolithography rapid shaping photosensitive resin.
At home, in recent ten years, there are many universities and scientific research institute, place to carry out the research of stereolithography rapid shaping photosensitive resin, obtained some achievements.But also not deeply, at present, domestic having two parts of patents of invention aspect the research of stereolithography rapid shaping photosensitive resin in research.Guangzhou Inst. of Machinery Science Haitao Liu, Zhong Hanrong and Xue Jidong have proposed " a kind of stereolithography rapid prototyping photosensitive resin ", and the number of applying for a patent is 200910040526.1.The king of Zhejiang Polytechnical University sea moral, Malaysian is outstanding, and Sun Xing equality has proposed " a kind of UV curing photosensitive resin for rapid moulding injection mold ", and the number of applying for a patent is 200910095846.7.In these two parts of applications; Used thinning agent was a trimethylolpropane triacrylate when they prepared photosensitive resin, tripropylene glycol diacrylate and 1,6 hexanediol diacrylate or the like; And these thinning agent volatility are big and pungency is big, and working environment is had certain pollution.Therefore, these two parts of patents all seem a bit not enough.
Summary of the invention
The objective of the invention is to overcome the weak point of above-mentioned prior art, the ethylene glycol diglycidylether diacrylate little volatility, that pungency is little and viscosity is low prepares stereolithography rapid shaping photosensitive resin as thinning agent.
The present invention realizes through following technical scheme.
Stereolithography rapid shaping photosensitive resin of the present invention is made up of following raw material by the quality proportioning:
5~30% ethylene glycol diglycidylether diacrylates
5~75% epoxy resin
5~55% oxetane compounds
1~12% cationic initiating agent
5~50% acrylic ester prepolymers
1~10% free radical type Photoepolymerizationinitiater initiater.
Epoxy resin according to the invention is bisphenol A type epoxy resin, phenol aldehyde type epoxy resin, cycloaliphatic epoxy resin or claims the one or more kinds of potpourris in the alicyclic epoxide compound.Preferred cycloaliphatic epoxy resin, for example, 3,4-epoxycyclohexyl formic acid-3 ', 4 '-epoxycyclohexyl methyl esters.
Oxetane compound of the present invention is a series of organism that contain oxetane groups; It comprises contains an oxetane groups; Two oxetane groups, the serial organism of three oxetane groups and a plurality of oxetane groups.Preferably contain two oxetane groups, the serial organism of three oxetane groups and a plurality of oxetane groups.
Cationic initiating agent of the present invention is salt compounded of iodine or sulfonium salt, wherein mainly is meant diaryl iodine hexafluorophosphate, diaryl iodine hexafluoro arsenate, diaryl iodine hexafluoro antimonate and triaryl matte hexafluorophosphate, triaryl matte hexafluoro arsenate, triaryl matte hexafluoro antimonate etc.Preferred triaryl matte hexafluorophosphate, triaryl matte hexafluoro arsenate and triaryl matte hexafluoro antimonate.
Acrylic ester prepolymer of the present invention is epoxy acrylate, urethane acrylate, polyester acrylate, amino acrylates, polyether acrylate, pure acrylic acid ester and organosilicon or Organic fluoride acrylic ester etc.Preferred epoxy acrylate mainly is meant bisphenol-a epoxy acrylate.
Free radical type Photoepolymerizationinitiater initiater of the present invention is for can cause the free radical type initiating agent that all unsaturated monomers that contain carbon-to-carbon double bond carry out polymerization.Preferred benzophenone, styrax dimethyl ether, chlorinated diphenyl ketone, 4-benzoyl-4 '-dimethyl diphenyl sulfide, 2-hydroxy-2-methyl-1-phenyl-1-acetone, 1-hydroxy cyclohexyl phenylketone or 2, the one or more kinds of potpourris in the 4-diethyl thioxanthone.
The present invention also provides the preparation method of stereolithography rapid shaping photosensitive resin, is that said material component is mixed by described quality proportioning; Then, heating, stirring promptly 20~80 ℃ of temperature, were stirred 5~120 minutes, made it to become the transparent faint yellow uniform liquid.
The synthetic method of ethylene glycol diglycidylether diacrylate of the present invention see " Huang Biwu etc. ethylene glycol diglycidylether diacrylate synthetic and use [J]. Central China University of Science and Technology's journal (natural science edition); 2004,32 (11): 27-29 ".
Ultimate principle of the present invention is following.
Now; The popular acrylate monomer as thinning agent is trimethylolpropane triacrylate (TMPTA), tripropylene glycol diacrylate (TPGDA) and 1 on the home market; 6-hexanediyl ester (HDDA) or the like; Because they have bigger smell and to bigger pungency of skin and bigger volatility, and will progressively be eliminated by market.Therefore, develop novel low smell and skin low irritant, hypotoxic acrylate monomer seemed extremely important.In view of the ethylene glycol diglycidylether diacrylate has the advantages that pungency is little, volatility is little and viscosity is low, can consider to select it to prepare stereolithography rapid shaping photosensitive resin as the thinning agent of photosensitive resin.
Has less shrinkability when solidifying for the stereolithography rapid shaping photosensitive resin that makes preparation; Product has higher precision; The present invention for suitably epoxy resin, oxetanes or their potpourris of adopting of prepolymer of photosensitive resin more; Suitably lack spent glycol diglycidyl ether diacrylate and acrylic ester prepolymer,, shrink little because the polymerization of epoxy resin, oxetanes is ring-opening polymerization; And the polymerization of ethylene glycol diglycidylether diacrylate and acrylic ester prepolymer is the polymerization of carbon-to-carbon double bond fracture becoming singly-bound, shrinks greatly.Yet; For the photosensitive resin that makes preparation has better photosensitivity; Need adopt ethylene glycol diglycidylether diacrylate and acrylic ester prepolymer as raw material as much as possible; Use epoxy resin, oxetanes as raw material less because ethylene glycol diglycidylether diacrylate and acrylic ester prepolymer under UV-irradiation its solidification rate faster than the solidification rate of epoxy resin and oxetanes.In order to make photosensitive resin can keep high precision property when the product and to take into account the photosensitivity of photosensitive resin; Should adopt epoxy resin and oxetanes to adopt ethylene glycol diglycidylether diacrylate and acrylic ester prepolymer again during the preparation photosensitive resin, good this balance of GPRS.In order to prepare stereolithography rapid shaping photosensitive resin, the present invention also selects ultraviolet initiator.Initiating agent preferably selects to comprise the free radical type initiating agent and the cationic initiating agent that causes epoxy resin and oxetanes polymerization of initiating methacrylates polymerization.When selecting initiating agent, to notice considering that initiating agent has response preferably to the specific wavelength ultraviolet light that ultraviolet laser sent, promptly the 355nm ultraviolet light had response preferably.
The present invention has following beneficial effect.
With respect to commercialization photosensitive resin in the past, its principal feature of photosensitive resin of the present invention's preparation is: at first, owing to be to add the ethylene glycol diglycidylether diacrylate as thinning agent, the photosensitive resin pungency is little few with volatile matter.Secondly, the photosensitivity of photosensitive resin is good, its critical exposure E cLess than 16.5mJ/cm 2Secondly, the precision of forming part is high, and the warp factor CF of forming part (6) is in ± 0.01 scope, and CF (11) is in ± 0.03 scope.
Adopt the photosensitive resin of the present invention's preparation can directly produce any complicated shape, have a high-precision part; And the preparation cost valency of this photosensitive resin is about 300 yuan an of per kilogram, far below the selling price (about 1500 yuans of per kilogram) of the photosensitive resin of DSM Somos company and Huntsman company.
Embodiment
Below in conjunction with embodiment, the present invention is done detailed description further, but implementation of the present invention is not limited thereto.
Embodiment 1.
1. in the special 5000 milliliters glass there-necked flask of stirrer and condenser pipe is housed, add 3,4-epoxycyclohexyl formic acid-3 ,, 4 ,-epoxycyclohexyl methyl esters 900 grams; Bisphenol A type epoxy resin (E-51) 600 grams, 3,3-[oxygen base dimethylene]-two [3-ethyl] oxetanes 400 grams; Bisphenol-a epoxy acrylate (EA-612) 680 grams; Ethylene glycol diglycidylether diacrylate 150 grams, styrax dimethyl ether 100 grams, triaryl matte hexafluoro antimonate 170 grams.
2. be heated to 50 ℃, stirred 30 minutes, make it to become the transparent faint yellow uniform liquid, this liquid is a kind of photosensitive resin of preparation.Record its critical exposure E cBe 16.2 mJ/cm 2, method of testing be adopt " Zhao Yi. the experimental study of photosensitive resin characteristic [J] in the laser fast forming. polymer material science and engineering, 2004,20 (1): 184-186 " institute's reported method.
3. the SLA-3500 type Ultra-Violet Laser that utilizes 3D Systems company to produce has solidified the rapid shaping equipment making some test blocks then, are in the 500 milliwatt ultraviolet casees at power, and these test blocks were solidified 90 minutes in the back.Record their warp factor CF (6)=0.01, CF (11)=0.03.For the rapid-result type photosensitive resin of Ultra-Violet Laser quick solidifying make the precision evaluation standard of part existing popular be the warp factor evaluation method, what its method adopted is the method for being formulated in second international quick shaping meeting holding in 1991.
Embodiment 2.
1. in the special 5000 milliliters glass there-necked flask of stirrer and condenser pipe is housed, add 3,4-epoxycyclohexyl formic acid-3 ,, 4 ,-epoxycyclohexyl methyl esters 1000 grams; Bisphenol A type epoxy resin (E-51) 500 grams, 3,3-[oxygen base dimethylene]-two [3-ethyl] oxetanes 400 grams; Bisphenol-a epoxy acrylate (EA-612) 530 grams; Ethylene glycol diglycidylether diacrylate 300 grams, 2-hydroxy-2-methyl-1-phenyl-1-acetone 100 grams, triaryl matte hexafluoro antimonate 170 grams.
2. be heated to 40 ℃, stirred 30 minutes, make it to become the transparent faint yellow uniform liquid, this liquid is a kind of photosensitive resin of preparation.Record its critical exposure E cBe 15.4 mJ/cm 2
3. the SLA-3500 type Ultra-Violet Laser that utilizes 3D Systems company to produce has solidified the rapid shaping equipment making some test blocks then, are in the 500 milliwatt ultraviolet casees at power, and these test blocks were solidified 90 minutes in the back.Record their warp factor CF (6)=0.01, CF (11)=-0.02.
Embodiment 3.
1. in the special 5000 milliliters glass there-necked flask of stirrer and condenser pipe is housed, add 3,4-epoxycyclohexyl formic acid-3 ,, 4 ,-epoxycyclohexyl methyl esters 1000 grams; Bisphenol A type epoxy resin (E-51) 400 grams, 3,3-[oxygen base dimethylene]-two [3-ethyl] oxetanes 500 grams; Bisphenol-a epoxy acrylate (EA-612) 430 grams; Ethylene glycol diglycidylether diacrylate 400 grams, styrax dimethyl ether 100 grams, triaryl matte hexafluoro antimonate 170 grams.
2. be heated to 50 ℃, stirred 20 minutes, make it to become the transparent faint yellow uniform liquid, this liquid is a kind of photosensitive resin of preparation.Record its critical exposure E cBe 14.6 mJ/cm 2
3. the SLA-3500 type Ultra-Violet Laser that utilizes 3D Systems company to produce has solidified the rapid shaping equipment making some test blocks then, are in the 500 milliwatt ultraviolet casees at power, and these test blocks were solidified 90 minutes in the back.Record their warp factor CF (6)=-0.01, CF (11)=0.02.
Embodiment 4.
1. in the special 5000 milliliters glass there-necked flask of stirrer and condenser pipe is housed, add 3,4-epoxycyclohexyl formic acid-3 ,, 4 ,-epoxycyclohexyl methyl esters 1000 grams; Bisphenol A type epoxy resin (E-51) 400 grams, 3,3-[oxygen base dimethylene]-two [3-ethyl] oxetanes 400 grams; Bisphenol-a epoxy acrylate (EA-612) 480 grams; Ethylene glycol diglycidylether diacrylate 450 grams, 1-hydroxy cyclohexyl phenylketone 100 grams, triaryl matte hexafluoro antimonate 170 grams.
2. be heated to 35 ℃, stirred 60 minutes, make it to become the transparent faint yellow uniform liquid, this liquid is a kind of photosensitive resin of preparation.Record its critical exposure E cBe 13.6 mJ/cm 2
3. the SLA-3500 type Ultra-Violet Laser that utilizes 3D Systems company to produce has solidified the rapid shaping equipment making some test blocks then, are in the 500 milliwatt ultraviolet casees at power, and these test blocks were solidified 90 minutes in the back.Record their warp factor CF (6)=0.01, CF (11)=-0.01.
Embodiment 5.
1. in the special 5000 milliliters glass there-necked flask of stirrer and condenser pipe is housed, add 3,4-epoxycyclohexyl formic acid-3 ,, 4 ,-epoxycyclohexyl methyl esters 1000 grams; Bisphenol A type epoxy resin (E-51) 450 grams, 3,3-[oxygen base dimethylene]-two [3-ethyl] oxetanes 350 grams; Bisphenol-a epoxy acrylate (EA-612) 430 grams; Ethylene glycol diglycidylether diacrylate 500 grams, 1-hydroxy cyclohexyl phenylketone 95 grams, triaryl matte hexafluoro antimonate 175 grams.
2. be heated to 65 ℃, stirred 10 minutes, become the transparent faint yellow uniform liquid, this liquid is a kind of photosensitive resin of preparation.Record its critical exposure E cBe 12.9 mJ/cm 2
3. the SLA-3500 type Ultra-Violet Laser that utilizes 3D Systems company to produce has solidified the rapid shaping equipment making some test blocks then, are in the 500 milliwatt ultraviolet casees at power, and these test blocks were solidified 90 minutes in the back.Record their warp factor CF (6)=-0.01, CF (11)=-0.02.
The foregoing description is a preferred implementation of the present invention; But embodiment of the present invention is not restricted to the described embodiments; Other any do not deviate from spirit of the present invention with away from the change of being made down, modification, substitute, combination, simplify; All should be the substitute mode of equivalence, be included within protection scope of the present invention.

Claims (12)

1. stereolithography rapid shaping photosensitive resin is characterized in that being made up of following raw material by the quality proportioning:
5~30% ethylene glycol diglycidylether diacrylates
5~75% epoxy resin
5~55% oxetane compounds
1~12% cationic initiating agent
5~50% acrylic ester prepolymers
1~10% free radical type Photoepolymerizationinitiater initiater.
2. stereolithography rapid shaping photosensitive resin according to claim 1 is characterized in that said epoxy resin is bisphenol A type epoxy resin, phenol aldehyde type epoxy resin, cycloaliphatic epoxy resin or claims the one or more kinds of potpourris in the alicyclic epoxide compound.
3. stereolithography rapid shaping photosensitive resin according to claim 2 is characterized in that said epoxy resin is 3,4-epoxycyclohexyl formic acid-3 ', 4 '-epoxycyclohexyl methyl esters.
4. stereolithography rapid shaping photosensitive resin according to claim 1 is characterized in that described oxetane compound is the organism that contains oxetane groups.
5. stereolithography rapid shaping photosensitive resin according to claim 4 is characterized in that described oxetane compound is the organism that contains two oxetane groups, three oxetane groups or a plurality of oxetane groups.
6. stereolithography rapid shaping photosensitive resin according to claim 1 is characterized in that described cationic initiating agent is salt compounded of iodine or sulfonium salt.
7. stereolithography rapid shaping photosensitive resin according to claim 6 is characterized in that described cationic initiating agent is diaryl iodine hexafluorophosphate, diaryl iodine hexafluoro arsenate, diaryl iodine hexafluoro antimonate, triaryl matte hexafluorophosphate, triaryl matte hexafluoro arsenate or triaryl matte hexafluoro antimonate.
8. stereolithography rapid shaping photosensitive resin according to claim 1 is characterized in that described acrylic ester prepolymer is epoxy acrylate, urethane acrylate, polyester acrylate, amino acrylates, polyether acrylate, pure acrylic acid ester, organosilicon or Organic fluoride acrylic ester.
9. stereolithography rapid shaping photosensitive resin according to claim 8 is characterized in that described acrylic ester prepolymer is a bisphenol-a epoxy acrylate.
10. stereolithography rapid shaping photosensitive resin according to claim 1 is characterized in that described free radical type Photoepolymerizationinitiater initiater is for can cause the free radical type initiating agent that all unsaturated monomers that contain carbon-to-carbon double bond carry out polymerization.
11. stereolithography rapid shaping photosensitive resin according to claim 10 is characterized in that described free radical type Photoepolymerizationinitiater initiater is benzophenone, styrax dimethyl ether, chlorinated diphenyl ketone, 4-benzoyl-4 '-dimethyl diphenyl sulfide, 2-hydroxy-2-methyl-1-phenyl-1-acetone, 1-hydroxy cyclohexyl phenylketone or 2, the one or more kinds of potpourris in the 4-diethyl thioxanthone.
12. the preparation method of each described stereolithography rapid shaping photosensitive resin of claim 1-11 is characterized in that said material component is mixed by described quality proportioning; Then, heating, stirring promptly 20~80 ℃ of temperature, were stirred 5~120 minutes, made it to become the transparent faint yellow uniform liquid.
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CN102981362A (en) * 2012-11-14 2013-03-20 南昌大学 Method using 4 and 5-cyclohexene oxide-1 and 2-dioctyl phthalate glycidyl ester as prepolymer to prepare three-dimensional lithography fast forming photosensitive resin and application
CN104250422A (en) * 2013-06-26 2014-12-31 合肥杰事杰新材料股份有限公司 Photosensitive resin used in 3D printing, and its preparation method
CN105404095A (en) * 2015-12-23 2016-03-16 河南工程学院 Washable ultraviolet laser curing and rapid prototyping photosensitive resin and preparation method thereof
CN105399908A (en) * 2015-12-23 2016-03-16 河南工程学院 New UV laser curing rapid molding photosensitive resin and preparation method thereof
CN106221177A (en) * 2016-07-26 2016-12-14 苏州秉创科技有限公司 A kind of injecting type 3D prints photo-curing material
CN107357136A (en) * 2017-08-23 2017-11-17 广西众昌树脂有限公司 Photosensitive liquid resin
CN107698722A (en) * 2016-08-08 2018-02-16 惠展电子材料(上海)有限公司 Photosensitive resin of ultraviolet laser solidification and preparation method thereof
CN108314911A (en) * 2017-01-17 2018-07-24 常州格林感光新材料有限公司 A kind of UVLED curable wood coatings
CN109467651A (en) * 2018-11-07 2019-03-15 华东理工大学华昌聚合物有限公司 Light-cured epoxy vinyl ester resin and its synthetic method

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102981362A (en) * 2012-11-14 2013-03-20 南昌大学 Method using 4 and 5-cyclohexene oxide-1 and 2-dioctyl phthalate glycidyl ester as prepolymer to prepare three-dimensional lithography fast forming photosensitive resin and application
CN104250422A (en) * 2013-06-26 2014-12-31 合肥杰事杰新材料股份有限公司 Photosensitive resin used in 3D printing, and its preparation method
CN105404095A (en) * 2015-12-23 2016-03-16 河南工程学院 Washable ultraviolet laser curing and rapid prototyping photosensitive resin and preparation method thereof
CN105399908A (en) * 2015-12-23 2016-03-16 河南工程学院 New UV laser curing rapid molding photosensitive resin and preparation method thereof
CN106221177A (en) * 2016-07-26 2016-12-14 苏州秉创科技有限公司 A kind of injecting type 3D prints photo-curing material
CN107698722A (en) * 2016-08-08 2018-02-16 惠展电子材料(上海)有限公司 Photosensitive resin of ultraviolet laser solidification and preparation method thereof
CN108314911A (en) * 2017-01-17 2018-07-24 常州格林感光新材料有限公司 A kind of UVLED curable wood coatings
CN107357136A (en) * 2017-08-23 2017-11-17 广西众昌树脂有限公司 Photosensitive liquid resin
CN109467651A (en) * 2018-11-07 2019-03-15 华东理工大学华昌聚合物有限公司 Light-cured epoxy vinyl ester resin and its synthetic method
CN109467651B (en) * 2018-11-07 2021-01-15 华东理工大学华昌聚合物有限公司 Light-cured epoxy vinyl ester resin and synthetic method thereof

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