Zhu Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Zhu Liu has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
- Guocong Liu
School of Chemistry and Materials Engineering, Huizhou University, Huizhou, China
1 shared publication - Haibo Wu
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China
1 shared publication Hao Cao
School of Chemistry and Materials Engineering, Huizhou University, Huizhou, China
1 shared publication- Hongping Xiang
School of Materials and Energy, Guangdong University of Technology, Guangzhou, China
1 shared publication - Jiao Zou
School of Chemistry and Materials Engineering, Huizhou University, Huizhou, Guangdong, 516007, China
1 shared publication - Jinyu Yang
School of Chemistry and Materials Engineering, Huizhou University, Huizhou 516007, China
1 shared publication
Latest Publications
- Open Access
Low Shrinkage Transparent UV-Cured 3D Printing Hard Silicone Resins
Acrylated silicone elastomers for UV-curing 3D printing have gathered considerable attention in biomedical applications due to their exceptional mechanical and thermal stability. However, traditional manufacturing methods for these resins often face challenges such as stringent conditions and self-polymerization. In this study, various acrylate silicone resins (LMDT-AE) and silicone oils (PDMS-AE) were synthesized through ring-opening hydrolysis-polycondensation. The structures of LMDT-AE and PDMS-AE, with varying AE contents (molar ratio of organic groups to silicon atoms), were characterized using FTIR, 1H NMR, 13C NMR, and GPC. Additionally, their physical properties, including viscosity, density, refractive index, and transparency, were thoroughly examined. The 3D-AE silicone resin composed of LMDT-AE-2.0 and PDMS-AE-20/1, in a mass ratio of 2:1, demonstrated superior mechanical properties, thermal stability, and curing shrinkage rate compared to other formulations. This curing silicone resin is capable of producing 3D physical entities with smooth surfaces and well-defined contours. It is shown that the successful preparation of transparent and high-strength UV-cured silicone resin based on free radical polymerization can provide a potential path for high-precision biological 3D printing.
Open AccessLow Shrinkage Transparent UV-Cured 3D Printing Hard Silicone Resins
Acrylated silicone elastomers for UV-curing 3D printing have gathered considerable attention in biomedical applications due to their exceptional mechanical and thermal stability. However, traditional manufacturing methods for these resins often face challenges such as stringent conditions and self-polymerization. In this study, various acrylate silicone resins (LMDT-AE) and silicone oils (PDMS-AE) were synthesized through ring-opening hydrolysis-polycondensation. The structures of LMDT-AE and PDMS-AE, with varying AE contents (molar ratio of organic groups to silicon atoms), were characterized using FTIR, 1H NMR, 13C NMR, and GPC. Additionally, their physical properties, including viscosity, density, refractive index, and transparency, were thoroughly examined. The 3D-AE silicone resin composed of LMDT-AE-2.0 and PDMS-AE-20/1, in a mass ratio of 2:1, demonstrated superior mechanical properties, thermal stability, and curing shrinkage rate compared to other formulations. This curing silicone resin is capable of producing 3D physical entities with smooth surfaces and well-defined contours. It is shown that the successful preparation of transparent and high-strength UV-cured silicone resin based on free radical polymerization can provide a potential path for high-precision biological 3D printing.
- 26 February 2025
- Published by Springer Nature in Journal of Polymer Research
- Vol. 32 (3) , 1-9
Preparation of transparent CO2 copolymer diol and its properties on waterborne polyurethane
- 26 February 2025
- Published by Springer Nature in Journal of Polymer Research
- Vol. 32 (3) , 1-9
Preparation of transparent CO2 copolymer diol and its properties on waterborne polyurethane
- Open Access
- 27 July 2024
- Published by MDPI AG in Nanomaterials
- Vol. 14 (15) , 1255
Multi-Stimuli-Responsive Fluorescent Molecule with AIE and TICT Properties Based on 1,8-Naphthalimide
A multi-stimuli responsive fluorophore, named NBDNI, was developed by constructing a 1,8-naphthalimide derivative in which a rotatable electron-donating N,N-dimethylaniline group attached to its 4-position. This molecular structure endowed NBDNI with aggregate-induced emission (AIE) and twisted intramolecular charge transfer (TICT) properties, enabling remarkable fluorescence changes in response to multiple external stimuli: (i) sensitivity to polarity in various solvent systems and polymer matrix; (ii) significant fluorescence response and excellent linearity towards temperature changes in solution; (iii) distinct switch of fluorescence color upon acid and base treatments; (iv) reversible mechanochromism behavior in the solid state. Moreover, the mechanisms underlying the aforementioned stimuli-responsive phenomena have been proposed based on comprehensive systematic measurements. Furthermore, preliminary applications such as fluorescence thermometry and acid/base test paper have been demonstrated. This research will bring about new opportunities for the development of novel stimuli-responsive luminescent materials.
- 27 July 2024
- Published by MDPI AG in Nanomaterials
- Vol. 14 (15) , 1255
Open AccessMulti-Stimuli-Responsive Fluorescent Molecule with AIE and TICT Properties Based on 1,8-Naphthalimide
A multi-stimuli responsive fluorophore, named NBDNI, was developed by constructing a 1,8-naphthalimide derivative in which a rotatable electron-donating N,N-dimethylaniline group attached to its 4-position. This molecular structure endowed NBDNI with aggregate-induced emission (AIE) and twisted intramolecular charge transfer (TICT) properties, enabling remarkable fluorescence changes in response to multiple external stimuli: (i) sensitivity to polarity in various solvent systems and polymer matrix; (ii) significant fluorescence response and excellent linearity towards temperature changes in solution; (iii) distinct switch of fluorescence color upon acid and base treatments; (iv) reversible mechanochromism behavior in the solid state. Moreover, the mechanisms underlying the aforementioned stimuli-responsive phenomena have been proposed based on comprehensive systematic measurements. Furthermore, preliminary applications such as fluorescence thermometry and acid/base test paper have been demonstrated. This research will bring about new opportunities for the development of novel stimuli-responsive luminescent materials.