Smart Structures—Additive Manufacturing of Stimuli-Responsive Hydrogels for Adaptive Packings

2020 ◽  
Vol 59 (43) ◽  
pp. 19458-19464
Author(s):  
Xihua Hu ◽  
Claas Spille ◽  
Michael Schlüter ◽  
Irina Smirnova
Micromachines ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 32
Author(s):  
Yufeng Tao ◽  
Chengchangfeng Lu ◽  
Chunsan Deng ◽  
Jing Long ◽  
Yunpeng Ren ◽  
...  

Rapid fabricating and harnessing stimuli-responsive behaviors of microscale bio-compatible hydrogels are of great interest to the emerging micro-mechanics, drug delivery, artificial scaffolds, nano-robotics, and lab chips. Herein, we demonstrate a novel femtosecond laser additive manufacturing process with smart materials for soft interactive hydrogel micro-machines. Bio-compatible hyaluronic acid methacryloyl was polymerized with hydrophilic diacrylate into an absorbent hydrogel matrix under a tight topological control through a 532 nm green femtosecond laser beam. The proposed hetero-scanning strategy modifies the hierarchical polymeric degrees inside the hydrogel matrix, leading to a controllable surface tension mismatch. Strikingly, these programmable stimuli-responsive matrices mechanized hydrogels into robotic applications at the micro/nanoscale (<300 × 300 × 100 μm3). Reverse high-freedom shape mutations of diversified microstructures were created from simple initial shapes and identified without evident fatigue. We further confirmed the biocompatibility, cell adhesion, and tunable mechanics of the as-prepared hydrogels. Benefiting from the high-efficiency two-photon polymerization (TPP), nanometer feature size (<200 nm), and flexible digitalized modeling technique, many more micro/nanoscale hydrogel robots or machines have become obtainable in respect of future interdisciplinary applications.


2019 ◽  
Vol 4 (1) ◽  
pp. 91-102 ◽  
Author(s):  
Ryan T. Shafranek ◽  
Joel D. Leger ◽  
Song Zhang ◽  
Munira Khalil ◽  
Xiaodan Gu ◽  
...  

Directed self-assembly in polymeric hydrogels allows tunability of thermal response and viscoelastic properties.


2021 ◽  
Vol 5 (5) ◽  
pp. 119
Author(s):  
Stelios K. Georgantzinos ◽  
Georgios I. Giannopoulos ◽  
Panteleimon A. Bakalis

This paper aims to establish six-dimensional (6D) printing as a new branch of additive manufacturing investigating its benefits, advantages as well as possible limitations concerning the design and manufacturing of effective smart structures. The concept of 6D printing, to the authors’ best knowledge, is introduced for the first time. The new method combines the four-dimensional (4D) and five-dimensional (5D) printing techniques. This means that the printing process is going to use five degrees of freedom for creating the final object while the final produced material component will be a smart/intelligent one (i.e., will be capable of changing its shape or properties due to its interaction with an environmental stimulus). A 6D printed structure can be stronger and more effective than a corresponding 4D printed structure, can be manufactured using less material, can perform movements by being exposed to an external stimulus through an interaction mechanism, and it may learn how to reconfigure itself suitably, based on predictions via mathematical modeling and simulations.


Author(s):  
Ana C. Marques ◽  
Paulo J. Costa ◽  
Sérgia Velho ◽  
Maria H. Amaral

2018 ◽  
Vol 229 (9) ◽  
pp. 3715-3725 ◽  
Author(s):  
C. C. Benjamin ◽  
R. S. Lakes ◽  
W. C. Crone

Soft Matter ◽  
2019 ◽  
Vol 15 (23) ◽  
pp. 4662-4668 ◽  
Author(s):  
Xun Zhang ◽  
Jinguo Liu ◽  
Yuxia Gao ◽  
Jie Hao ◽  
Jun Hu ◽  
...  

Two gluconamide-tailored anthracene gelators 1 and 2 were found to form stable hydrogels which exhibited multiple responsive behaviours upon exposure to temperature, anions, light, electron-deficient chemicals and external stress.


2018 ◽  
Vol 5 (6) ◽  
pp. 1076-1081 ◽  
Author(s):  
Takayuki Hiratani ◽  
Osamu Kose ◽  
Wadood Y. Hamad ◽  
Mark J. MacLachlan

Stimuli-responsive hydrogels that respond to pressure and ionic strength were prepared with large mono-domain, nematic organization of cellulose nanocrystals (CNCs).


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