文献类型: 外文期刊
作者: Gao, Yi 1 ; Xu, Lei 4 ; Zhao, Yang 1 ; You, Zhengwei 1 ; Guan, Qingbao 1 ;
作者机构: 1.Donghua Univ, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai Belt & Rd Joint Lab Adv Fiber & Low Dime, Shanghai 201620, Peoples R China
2.Tsinghua Univ, Ctr Combust Energy, Beijing 100084, Peoples R China
3.Tsinghua Univ, Key Lab Thermal Sci & Power Engn MOE, Beijing 100084, Peoples R China
4.Jiangsu Acad Agr Sci, Inst Agr Facil & Equipment, Key Lab Protected Agr Engn Middle & Lower Reaches, Minist Agr & Rural Affairs, Nanjing 210014, Peoples R China
关键词: 3D printing preview; Photopolymerization kinetics; Biomedical applications; Dental materials; Epoxy acrylate
期刊名称:BIOACTIVE MATERIALS ( 影响因子:14.593; 五年影响因子:13.877 )
ISSN:
年卷期: 2020 年 5 卷 4 期
页码:
收录情况: SCI
摘要: The diversity of biomedical applications makes stereolithographic (SL) three-dimensional (3D) printing process complex. A strategy was developed to simulate the layer-by-layer fabrication of 3D printed products combining polymerization kinetic with reaction conditions to realize print preview. As a representative example, the typical UV-curable dental materials based on epoxy acrylate and photoinitiator with different molar ratios was exposed under varying intensity of UV light to verify the simulation results. A theoretical kinetics model containing oxygen inhibition was established. In-situ FTIR was employed to measure propagation and termination constants while coupled UV/vis was performed to examine the law of light attenuation during cure reaction, even with various colours and additives. Simulation results showed that the correlation coefficient square between the experiments and simulations of epoxy acrylate with 1%, 2% and 3% initiator upon 20 mW/cm(2) UV light are 0.8959, 0.9324 and 0.9337, respectively. Consequently, our simulation of photopolymerization for SL 3D printing successfully realized visualization of printing quality before practically printing the targeted biomedical objects with complex topology structures.
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