Radical inhibition in tomographic volumetric 3D printing for thiol-Ene photoresists: From Photorheology to printability

被引:0
作者
Thijssen, Quinten [1 ]
Ortega, Antonio Jaen [1 ]
Vieira, Ronierik Pioli [2 ]
Van Vlierberghe, Sandra [1 ]
机构
[1] Univ Ghent, Ctr Macromol Chem, Dept Organ & Macromol Chem, Polymer Chem & Biomat Grp, Krijgslaan 281 S4, B-9000 Ghent, Belgium
[2] Univ Estadual Campinas UNICAMP, Sch Chem Engn, Albert Einstein Ave 500, BR-13083852 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会; 比利时弗兰德研究基金会;
关键词
Volumetric; 3D-printing; Inhibition; Photorheology; Volumetric additive manufacturing; TEMPO; Kinetic modeling; RECIPROCITY LAW; PHOTOPOLYMERIZATION; MECHANISM; KINETICS; POLYMERIZATION; NITROXIDES; CHEMISTRY; OXIDES; STEP;
D O I
10.1016/j.reactfunctpolym.2024.106096
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The introduction of tomographic volumetric 3D printing is revolutionizing the manufacturing and bioprinting landscape by enabling the rapid creation of complex three-dimensional (biological) structures with high precision down to 20 mu m. Despite the recognized role of radical inhibition in volumetric 3D printing, a study of inhibition has remained elusive. Here, A comprehensive framework is presented to study the role of the widely reported radical inhibitor TEMPO in the volumetric 3D printability of a thiol-ene photocrosslinkable photoresist composed of triallyl isocyanurate (TTT) and pentaerythritol tetrakis(3-mercaptopropionate) (PETMP). Through photorheological measurements, kinetic modeling, FTIR spectroscopy, and validation via volumetric 3D printing, the relationship between inhibitor concentrations, the evolution of the shear moduli as well as the conversion as a function of light dose, and volumetric 3D printing is elucidated. The findings in this study provide a robust methodology for predicting optimal printing conditions of photoresists for tomographic volumetric 3D printing, obviating the need for extensive trial-and-error.
引用
收藏
页数:9
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