新潟大学工学部材料科学プログラム
新潟大学大学院自然科学研究科材料生産システム専攻
三俣研究室 Mitsumata laboratory
Dr. Tetsu Mitsumata
He received the PhD degree in Polymer Science in 1999 from Hokkaido University
under the direction of Prof. Y. Osada and Prof. J. P. Gong. After the PhD,
he studied stimuli-responsive polymer gels at Yamagata University as assistant
professor. In 2002, he joined the laboratory of Dr. P. Dekepper (CRPP Bordeaux
in France) to study nonlinear chemistry in solutions and gels. Now, He
works at the department of materials science and technology at Niigata
University as associate professor. He has published more than 70 scientific
papers, 17 review papers, 8 books, and 7 patents including international
patents, dedicated to Soft Materials, especially magnetic responsive gels
or elastomers. He has delivered invited lectures not only scientific conferences
but also manufacturing companies.
[Awards & Honors]
Encouragement award, Bridgestone soft material frontier prize (2010)
Best presented paper award, Chemical Evaluation and Research institute, Japan (2008)
Best presentation award, The Chemical Society of Japan (1999)
[Research & Project]
Viscoelastic response of magnetic soft materials
Stimulis responsive properties of synthetic and natural polymers
[Membership]
The Chemical Society of Japan
The Society of Polymer Science, Japan
The Materials Research Society of Japan
The Society of Rubber Science and Technology, Japan
[Selected Publications]
lonic state and chain conformation for aqueous solutions of supergiant
cyanobacterial polysaccharide, Phys. Rev., 87, 042607 (2013)
Magnetoelastic Behavior of Bimodal Magnetic Hydrogels Using Nonmagnetic
Partcles, Chem. Lett., 42, 50 (2013) Editor's choice
Magnetism and viscoelasticity of magnetic elastomers with wide range modulation
of dynamic modulus, Soft Matter, 9, 904 (2013)
Magnetic polyurethane elastomers with wide modulation of elasticity, Polym.
Chem., 2, 1063 (2011)
Thermosensitive solutions and gels consisting og Poly(vinyl alcohol) and
sodium silicate, Mater. Lett., 61, 3878 (2007)
pH-Response of Chitosan, k-Carrageenan, Carboxymethyl Cellulose Sodium
Salt Complex Hydrogels, Polymer, 44, 7103 (2003)
Solvent-Driven Chemical Motor, App. Phys. Lett., 73, 2366 (1998)
We have succeeded to synthesize magnetic polyurethane elastomers and investigated
the magnetorheological property, mechanical property, and degradation of
the elastomers. The magnetic elastomer exhibited a reversible increase
by facators of277 of the storage modulis and 96 of the loss modulus upon
a magnetic field of 500 mT, which were nearly the same level with magnetic
hydrogels demonstrating the giant magnetorheology. The magnetic elastomer
maintained the magnetic field response for half year after the synthesis.
In addition, the magnetic elastomer underwent high mechanical toughness
with a breaking strain exceeding 0.8, and did not show a permanent deformation
after removing the strain. These features clearly indicate that magnetic
elastomers are suitable for materiale working under the air, than magnetic
gels. We firmly believe that this magnetic elastomer which dramatically
prolonged the lifetime will be widely used in the magnetically controllable
smart devices in near future.
We have succeede to fabricate a magnetic actuator consisting of magnetic polyurethane elastomere that demonstrate the elongation-contraction behavior by magnetic fields. The magnetic elastomer lifted up a weight of 10 kg with a stroke of 1.6 mm by applying a magnetic field of 300 mT. The time constant for the lifting was 200 ms. The maximum displacement of elongation was 4 mm without applying weights. We firmly believe that the high-power magnetic elastomer would be useful for the magnetically-driven actuator in practical use.
We have investigated the electric and rheological properties of the aqueous solution of cyanobacterial megamolecules named sacran. The molecular weight of sacran is 1.6×107 g/mol. The sacran is an anionic polyelectrolyte which has carboxylate and sulfate groups on the saccharide chain. Above the concentrations of 0.1 wt %, the sacran chain formed a weak gel which exhibits macroscopic liquid crystal domains. The sacran solution demonstrates shear induced viscosity when a constant flow with low shear rates was applied. When the flow is stopped, the viscosity is recovered to the original viscosity within 5 min. This phenomenon can be seen in other polysaccharides, however the increment in the viscosity for sacran aqueous solution is huge. We are investigating the mechanism of the negative thixotropy of the giant polysaccharide sacran.
We have investigated the transparency for visible light
of a poly(vinyl alcohol) (PVA) aqueous solution in the presence of sodium
silicates (SS). The transparency of the aqueous solution dramatically changed
by varying temperature despite that neither aqueous solutions of PVA nor SS is
sensitive to temperature. The aqueous solution showed a lower critical solution
temperature (LCST) around 30 oC. The LCST depended on both concentrations of
PVA and sodium silicate. Below the LCST, the transmittance was thermally
irreversible. By a further increase in the temperature, the solution was
separated into two phases consisting of a phase rich in solvent and that in
solute; that is a coacervation. In the region of coacervation, the transmittance was thermally reversible. Reversible change
in the transmittance was realized corresponding to stepwise temperature
changes between 10 to 40 oC. A PVA gel swollen by the solution demonstrated
transparency change in response to temperature changes as well as the solution.