journal article·2019-11-10Open access

Synthesis, Characterization and Fiber Spinning of Poly (caffeic acid)

Daisuke Ishii, Tadahisa Iwata

Abstract

A melt-spinnable poly(caffeic acid) (PCA) was prepared by ester exchange reaction of acetylated caffeic acid at 180 ̊C for 4 h under vacuum. The PCA showed broad processing window between the glass transition temperature at 101 ̊C and 5-% weight decrease temperature at 313 ̊C. The PCA showed shear thinning in the molten state at 180 ̊C, reflecting the development of molecular orientation under shear. The melt-spun PCA fiber showed Young’s modulus of 1.3 to 2.0 GPa, tensile strength of ca. 50 MPa, and elongation at break of 4 to 5 %. The relatively low mechanical strength of the melt-spun fiber is attributed to the loose molecular orientation, that was reflected in the two-dimensional wide-angle X-ray scattering pattern showing the broad azimuthal distribution.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: biodegradable polymer synthesis and properties · Microplastics and Plastic Pollution · Fiber-reinforced polymer composites

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

Affiliations

Department of Chemistry for Life Sciences and Agriculture, Faculty of Life Sciences, Tokyo University of Agriculture

Science of Polymeric Materials, Department of Biomaterial Sciences, Graduate School of Agricultural and Life Sciences

References (11)

Show source-provided references
1. [1] T. Iwata, Macromol. Biosci. 5, 689 (2005).10.1002/mabi.200500066 ↗
2. [3] T. Kabe, T. Sugiura, T. Hikima, M. Takata, T. Iwata, J. Fiber. Sci. Technol., 74, 30 (2018).10.2115/fiberst.2018-0005 ↗
3. [4] L. F. Charbonneau, US patent 4230817 A (1980).
4. [5] H.-G. Elias and J. A. Palacios, Makromol. Chem. 186,1027 (1985).10.1002/macp.1985.021860513 ↗
5. [6] H. T. Tran, M. Matsusaki, D. J. Shi, T. Kaneko and M.Akashi, J. Biomater. Sci., Polym. Ed., 19, 75 (2008).10.1163/156856208783227668 ↗
6. [7] L. Mialon, A. G. Pemba, and S. A. Miller, Green Chem. 12, 1704 (2010).10.1039/c0gc00150c ↗
7. [8] S. A. Miller, ACS Macro Lett. 2, 550 (2013).10.1021/mz400207g ↗
8. [9] T. Kaneko, D. Kaneko and S. Wang, Plant Biotechnol. 27, 243 (2010).10.5511/plantbiotechnology.27.243 ↗
9. [10] D. Ishii, H. Maeda, H. Hayashi, T. Mitani, M. Shinohara, K. Yoshioka, T. Watanabe, ACS Symp. Ser., 1144, 237 (2013).10.1021/bk-2013-1144.ch017 ↗
10. [11] A. Pegoretti, A. Zanolli, C. Migliaresi, Comp. Sci. Technol., 66, 1970 (2006).10.1016/j.compscitech.2006.01.012 ↗
11. [12] I. Karakan, J. Appl. Polym. Sci. 100, 142 (2006).10.1002/app.22554 ↗