journal article·2016-12-13

Programmable Volume Phase Transition of Hydrogels Achieved by Large Thermal Hysteresis for Static-Motion Bilayer Actuators

Dowan Kim, Haneul Kim, Eunsu Lee, Kyeong Sik Jin, Jinhwan Yoon

Chemistry of Materials· Volume 28· Issue 23
Publisher page

Abstract

In order to achieve a hydrogel capable of programmable volume change, poly( N -isopropylacrylamide)- graft -methylcellulose hydrogel (PNIPAm- g -MC) was prepared through the grafting of PNIPAm onto a MC backbone and simultaneous cross-linking of the chains. PNIPAm- g -MC exhibited large thermal hysteresis in its volume change, which results from the stable hydrophobic junctions between the MC strands formed during heating. By combining photothermal magnetite nanoparticles as a heat transducer with the prepared hydrogel, programmable volume phase transition between the shrunken and swollen state could be triggered by visible light irradiation and excessive cooling, respectively. Based on this programmable feature, a bilayer actuator capable of static bending was fabricated. The developed programmable hydrogels are expected to provide a platform for the next generation of origami, microvalves, and drug delivery systems.
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Research context

OpenAlex topics: Advanced Materials and Mechanics · Hydrogels: synthesis, properties, applications · Micro and Nano Robotics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Dong-A University, 37 Nakdong-Daero 550beon-gil, Saha-gu, Busan 49315, Republic of Korea

Pohang Accelerator Laboratory, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea

Funding

National Research Foundation of Korea · Ministry of Education

References (31)

Show source-provided references
1. 10.1016/0079-6700(92)90023-R10.1016/0079-6700(92)90023-R ↗
2. 10.1021/la100020t10.1021/la100020t ↗
3. 10.3390/ma312514310.3390/ma3125143 ↗
4. 10.1039/C2PY20889J10.1039/C2PY20889J ↗
5. 10.1126/science.269.5223.52510.1126/science.269.5223.525 ↗
6. 10.1016/j.polymer.2010.10.03510.1016/j.polymer.2010.10.035 ↗
7. 10.1002/anie.20110672310.1002/anie.201106723 ↗
8. 10.1002/adfm.20120170810.1002/adfm.201201708 ↗
9. 10.1021/nn507426u10.1021/nn507426u ↗
10. 10.1039/c1sm00011j10.1039/c1sm00011j ↗
11. 10.1002/anie.20120269210.1002/anie.201202692 ↗
12. 10.1002/smll.20140047710.1002/smll.201400477 ↗
13. 10.1039/C4RA01537A10.1039/C4RA01537A ↗
14. 10.1038/srep1512410.1038/srep15124 ↗
15. 10.1002/adhm.20150032310.1002/adhm.201500323 ↗
16. 10.1038/srep0764610.1038/srep07646 ↗
17. 10.1021/la010917r10.1021/la010917r ↗
18. 10.1016/j.biomaterials.2003.09.07710.1016/j.biomaterials.2003.09.077 ↗
19. 10.1016/j.polymer.2005.05.12810.1016/j.polymer.2005.05.128 ↗
20. 10.1039/b909008h10.1039/b909008h ↗
21. 10.1295/polymj.37.23410.1295/polymj.37.234 ↗
22. 10.1021/jp102681q10.1021/jp102681q ↗
23. 10.1002/anie.20140210810.1002/anie.201402108 ↗
24. 10.1039/C4OB02654C10.1039/C4OB02654C ↗
25. 10.1021/ma00104a02710.1021/ma00104a027 ↗
26. 10.1021/ma00111a06210.1021/ma00111a062 ↗
27. 10.1039/C3SM52666F10.1039/C3SM52666F ↗
28. 10.1039/c0sm00434k10.1039/c0sm00434k ↗
29. 10.1016/j.ejpb.2013.05.01110.1016/j.ejpb.2013.05.011 ↗
30. 10.1007/BF0174668610.1007/BF01746686 ↗
31. 10.5935/0103-5053.2015016310.5935/0103-5053.20150163 ↗