This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Decker C. Kinetic study and new applications of UV radiation curing. Macromol Rapid Commun. 2003;23(18):1067–93. https://doi.org/10.1002/marc.200290014.DeckerCKinetic study and new applications of UV radiation curingMacromol Rapid Commun20032318106793https://doi.org/10.1002/marc.200290014.10.1002/marc.200290014Search in Google Scholar
Shirai M. Reworkable UV curing materials. Prog Organic Coat. 2007;58(2–3):158–65. https://doi.org/10.1016/j.porgcoat.2006.08.022.ShiraiMReworkable UV curing materialsProg Organic Coat2007582–315865https://doi.org/10.1016/j.porgcoat.2006.08.022.10.1016/j.porgcoat.2006.08.022Search in Google Scholar
Xie P, Hu L, He J, Kang W, Yang W. Mechanism and solutions of appearance defects on microfluidic chips manufactured by UV-curing assisted injection molding. J Polym Eng. 2017;37(5):493–503. https://doi.org/10.1515/polyeng-2016-0153.XiePHuLHeJKangWYangWMechanism and solutions of appearance defects on microfluidic chips manufactured by UV-curing assisted injection moldingJ Polym Eng2017375493503https://doi.org/10.1515/polyeng-2016-0153.10.1515/polyeng-2016-0153Search in Google Scholar
Sangermano M, Razza N, Crivello JV. Cationic UV-curing: Technology and applications. Macromol Mater Eng. 2014;299(7):775–93. https://doi.org/10.1002/mame.201300349.SangermanoMRazzaNCrivelloJVCationic UV-curing: Technology and applicationsMacromol Mater Eng2014299777593https://doi.org/10.1002/mame.201300349.10.1002/mame.201300349Search in Google Scholar
Kraft V, Schumann C, Salzmann D, Nopper H, Weyhe D, Schenk A. Towards realistic organ models for 3D printing and visualization. Curr Dir Biomed Eng. 2021;7(1):166–70. https://doi.org/10.1515/cdbme-2021-1036.KraftVSchumannCSalzmannDNopperHWeyheDSchenkATowards realistic organ models for 3D printing and visualizationCurr Dir Biomed Eng20217116670https://doi.org/10.1515/cdbme-2021-1036.10.1515/cdbme-2021-1036Search in Google Scholar
Stansbury JW, Idacavage MJ. 3D printing with polymers: challenges among expanding options and opportunities. Den Mater. 2016;32(1):54–64. https://doi.org/10.1016/j.dental.2015.09.018.StansburyJWIdacavageMJ3D printing with polymers: challenges among expanding options and opportunitiesDen Mater20163215464https://doi.org/10.1016/j.dental.2015.09.018.10.1016/j.dental.2015.09.01826494268Search in Google Scholar
Zhang LJ, Wu CB, Yang F, Geng XY, Li MQ, Xiao JJ. Preparation and characterization of UV curable hybrid system based on free radical and cationic mechanism. Appl Mech Mater. 2014;470:141–45. https://doi.org/10.4028/www.scientific.net/AMM.470.141.ZhangLJWuCBYangFGengXYLiMQXiaoJJPreparation and characterization of UV curable hybrid system based on free radical and cationic mechanismAppl Mech Mater201447014145https://doi.org/10.4028/www.scientific.net/AMM.470.141.10.4028/www.scientific.net/AMM.470.141Search in Google Scholar
Park YJ, Lim DH, Kim HJ, Park DS, Sung IK. UV and thermal-curing behaviors of dual-curable adhesives based on epoxy acrylate oligomers. Int J Adhes Adhesives. 2012;29(7):710–7. https://doi.org/10.1016/j.ijadhadh.2009.02.001.ParkYJLimDHKimHJParkDSSungIKUV and thermal-curing behaviors of dual-curable adhesives based on epoxy acrylate oligomersInt J Adhes Adhesives20122977107https://doi.org/10.1016/j.ijadhadh.2009.02.001.10.1016/j.ijadhadh.2009.02.001Search in Google Scholar
Cho JD, Ju HT, Hong JW. Photocuring kinetics of UV-initiated free-radical photopolymerizations with and without silica nanoparticles. J Polym Sci Part A. 2010;43(3):658–70. https://doi.org/10.1002/pola.20529.ChoJDJuHTHongJWPhotocuring kinetics of UV-initiated free-radical photopolymerizations with and without silica nanoparticlesJ Polym Sci Part A201043365870https://doi.org/10.1002/pola.20529.10.1002/pola.20529Search in Google Scholar
Temel G, Enginol B, Aydin M, Balta DK, Arsu N. Photopolymerization and photophysical properties of amine linked benzophenone photoinitiator for free radical polymerization. J Photochem Photobiol A. 2011;219(1):26–31. https://doi.org/10.1016/j.jphotochem.2011.01.012.TemelGEnginolBAydinMBaltaDKArsuNPhotopolymerization and photophysical properties of amine linked benzophenone photoinitiator for free radical polymerizationJ Photochem Photobiol A201121912631https://doi.org/10.1016/j.jphotochem.2011.01.012.10.1016/j.jphotochem.2011.01.012Search in Google Scholar
Sipani V, Kirsch A, Scranton AB. Dark cure studies of cationic photopolymerizations of epoxides: Characterization of kinetic rate constants at high conversions. J Polym Sci Part A. 2004;42(17):4409–16. https://doi.org/10.1002/pola.20209.SipaniVKirschAScrantonABDark cure studies of cationic photopolymerizations of epoxides: Characterization of kinetic rate constants at high conversionsJ Polym Sci Part A20044217440916https://doi.org/10.1002/pola.20209.10.1002/pola.20209Search in Google Scholar
Noè C, Hakkarainen M, Sangermano M. Cationic UV-curing of epoxidized biobased resins. Polymers. 2020;13(1):89. https://doi.org/10.3390/polym13010089.NoèCHakkarainenMSangermanoMCationic UV-curing of epoxidized biobased resinsPolymers202013189https://doi.org/10.3390/polym13010089.10.3390/polym13010089Search in Google Scholar
Noè C, Malburet S, Milani E, Bouvet-Marchand A, Graillot A, Sangermano M. Cationic UV-curing of epoxidized cardanol derivatives. Polym Int. 2020;69(8):668–74. https://doi.org/10.1002/pi.6031.NoèCMalburetSMilaniEBouvet-MarchandAGraillotASangermanoMCationic UV-curing of epoxidized cardanol derivativesPolym Int202069866874https://doi.org/10.1002/pi.6031.10.1002/pi.6031Search in Google Scholar
Cho JD, Hong JW. Curing kinetics of UV-initiated cationic photopolymerization of divinyl ether photosensitized by thioxanthone. J Appl Polym Sci. 2010;97(3):1345–51. https://doi.org/10.1002/app.21838.ChoJDHongJWCuring kinetics of UV-initiated cationic photopolymerization of divinyl ether photosensitized by thioxanthoneJ Appl Polym Sci2010973134551https://doi.org/10.1002/app.21838.10.1002/app.21838Search in Google Scholar
Heilen W, Herrwerth S. Silicone resins and their combinations. Hannover, Germany: Vincentz Network, 2015.HeilenWHerrwerthSSilicone resins and their combinationsHannover, GermanyVincentz Network2015Search in Google Scholar
Bajaj P, Gupta DC. Copolymerization of styrene and acrylonitrile with functional silanes. Eur Polym J. 1979;15(3):271–5. https://doi.org/10.1016/0014-3057(79)90175-7.BajajPGuptaDCCopolymerization of styrene and acrylonitrile with functional silanesEur Polym J19791532715https://doi.org/10.1016/0014-3057(79)90175-7.10.1016/0014-3057(79)90175-7Search in Google Scholar
Murias P, Maciejewski H, Galina H. Epoxy resins modified with reactive low molecular weight siloxanes. Eur Polym J. 2012;48(4):769–73. https://doi.org/10.1016/j.eurpolymj.2012.01.009.MuriasPMaciejewskiHGalinaHEpoxy resins modified with reactive low molecular weight siloxanesEur Polym J201248476973https://doi.org/10.1016/j.eurpolymj.2012.01.009.10.1016/j.eurpolymj.2012.01.009Search in Google Scholar
Yu Z, Cui A, Zhao P, Wei H, Hu F. Preparation and properties studies of UV-curable silicone modified epoxy resin composite system. J Appl Biomater Fundam Mater. 2018;16(1):170–6. https://doi.org/10.1177/2280800017753053.YuZCuiAZhaoPWeiHHuFPreparation and properties studies of UV-curable silicone modified epoxy resin composite systemJ Appl Biomater Fundam Mater20181611706https://doi.org/10.1177/2280800017753053.10.1177/228080001775305329618261Search in Google Scholar
Huang B, Han L, Wu B, Chen H, Zhou W, Lu Z. Application of Bis [2-(3,4-epoxycyclohexyl) ethyl]octamethyltetrasiloxane in the preparation of a photosensitive resin for stereolithography 3D printing. J Wuhan Univ Technol. 2019;34(6):236–44. https://doi.org/10.1007/s11595-019-2215-7.HuangBHanLWuBChenHZhouWLuZApplication of Bis [2-(3,4-epoxycyclohexyl) ethyl]octamethyltetrasiloxane in the preparation of a photosensitive resin for stereolithography 3D printingJ Wuhan Univ Technol201934623644https://doi.org/10.1007/s11595-019-2215-7.10.1007/s11595-019-2215-7Search in Google Scholar
Khalaf HI, Wady AN, Daham HK. Synthesis and characterization of new optically active poly(amideimide) s derived from n,n′-(pyromellitoyl) bis-l-tyrosine and various diamines. Mater Sci. 2013;31(1):43–51. https://doi.org/10.2478/s13536-012-0077-1.KhalafHIWadyANDahamHKSynthesis and characterization of new optically active poly(amideimide) s derived from n,n′-(pyromellitoyl) bis-l-tyrosine and various diaminesMater Sci20133114351https://doi.org/10.2478/s13536-012-0077-1.10.2478/s13536-012-0077-1Search in Google Scholar
Altowyan AS, Ahmed HA, Gomha SM, Mostafa AM. Optical and thermal investigations of new schiff base/ester systems in pure and mixed states. Polymers. 2021;13(11):1687. https://doi.org/10.3390/polym13111687.AltowyanASAhmedHAGomhaSMMostafaAMOptical and thermal investigations of new schiff base/ester systems in pure and mixed statesPolymers202113111687. https://doi.org/10.3390/polym13111687.10.3390/polym13111687819680934067245Search in Google Scholar
Suresh J, Karthik S, Arun A. Photocrosslinkable polymer based on 4-(3-(2,4-dichlorophenyl)-3-oxoprop-1-enyl) phenylacrylate: Synthesis, reactivity ratio, and crosslinking studies. Mater Sci. 2016;34(4):834–44. https://doi.org/10.1515/msp-2016-0117.SureshJKarthikSArunAPhotocrosslinkable polymer based on 4-(3-(2,4-dichlorophenyl)-3-oxoprop-1-enyl) phenylacrylate: Synthesis, reactivity ratio, and crosslinking studiesMater Sci201634483444https://doi.org/10.1515/msp-2016-0117.10.1515/msp-2016-0117Search in Google Scholar
Shi Y, Ma W, Wang J, Mo J. 2-ethy-4-methylimidazole terminated polyurethane prepolymer as functional latent curing agents for epoxy resin crosslinking. J Macromol Sci Part A. 2019;56(8):750–8. https://doi.org/10.1080/10601325.2019.1586438.ShiYMaWWangJMoJ2-ethy-4-methylimidazole terminated polyurethane prepolymer as functional latent curing agents for epoxy resin crosslinkingJ Macromol Sci Part A20195687508https://doi.org/10.1080/10601325.2019.1586438.10.1080/10601325.2019.1586438Search in Google Scholar
Rusu MC, Block C, Van Assche G, Van Mele B. Influence of temperature and UV intensity on photo-polymerization reaction studied by photo-DSC. J Thermal Anal Calorimetry. 2012;110(1):287–94. https://doi.org/10.1007/s10973-012-2465-5.RusuMCBlockCVan AsscheGVan MeleBInfluence of temperature and UV intensity on photo-polymerization reaction studied by photo-DSCJ Thermal Anal Calorimetry2012110128794https://doi.org/10.1007/s10973-012-2465-5.10.1007/s10973-012-2465-5Search in Google Scholar