2018-Sustainable Industrial Processing Summit
SIPS2018 Volume 4. Mamalis Intl. Symp. / Advanced Manufacturing
| Editors: | F. Kongoli, A. G. Mamalis, K. Hokamoto |
| Publisher: | Flogen Star OUTREACH |
| Publication Year: | 2018 |
| Pages: | 352 pages |
| ISBN: | 978-1-987820-88-1 |
| ISSN: | 2291-1227 (Metals and Materials Processing in a Clean Environment Series) |
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Nanaocomposites Based on Graphene/Polymer for 3D Printers
Natia Jalagonia1; Nino Darakhvelidze2; Avtandil Sichinava2; Ekaterine Sanaia2; Marcello Casa3; Leila Kalatozishvili2;1ILIA VEKUA SOKHUMI INSTITUTE OF PHYSICS AND TECHNOLOGY, Tbilisi, Georgia; 2ILIA VEKUA SUKHUMI INSTITUTE OF PHYSICS AND TECHNOLOGY, Tbilisi, Georgia; 3, Salerno, Italy;
Type of Paper: Regular
Id Paper: 342
Topic: 48
Abstract:
Three-dimensional (3D) printing is often considered synonymous with additive manufacturing. Several types of 3D printer are known where polymers are usually used. Stereolithography (SLA) employs a single beam laser to polymerize or crosslink a photopolymer resin. By drawing on the liquid photopolymer resin with a light beam, thin layers of polymer are stacked layer by layer. Elastomer based on polydimethysiloxanes (PDMS) are an important class of materials, because of properties such as chemical inertness, flexibility, and optical transparence. In addition, they have a very low surface tension (20.4 mN/m) and glass transition temperatures (146 K). it is possible to print a support material that holds the PDMS prepolymer in place until it can be cured by UV light using a photoactive cross-linking agent. It is possible to graft photoactive group on PDMS backbone and obtain a new UV curable polymer [1,2].
The aim of the presented work is to obtain photopolymers based on PDMS [3]. For this purpose, we have conducted a hydrosilylation reaction of polymethylhydrosiloxane (PMHS) with allyl acrylate and vinyltriethoxysilane in the presence of Karstedta's catalyst in Toluene. The obtained polymer is liquid, which is well soluble in organic solvents with specific viscosity ηsp = 0.4. The end of reaction was tested by FTIR, where peak at 1260 cm-1 disappears, which belongs to Si-H bonds. After this the polymer is distilled in vacuum, about 1% of a cross-linking agent was added and curried by UV during 1 h.
Keywords:
Multifunctional materials; Polymers;References:
[1] J. T. Sheridan, Photopolymers Materials (Light Sensitive Organic Materials): Characterization and Application to 3D Optical Fabrication and Data Storage. [Online] Available at: http://www.ucd.ie/t4cms/Photopolymers%20Materials_%20Characterization%20and %20Application%20to%203D%20Optical%20Fabrication%20and%20Data%20Stora ge.pdf. [Accessed: 07.10.2013].[2] B. Thavornyutikarn, R. Nonthabenjawan, P. Ngamdee, W. Janvikul. Synthesis, Characterization and Crosslinking of Dual-Curable Siloxane Copolymers. Journal of Metals, Materials and Minerals. 18, 2, 213-218, 2008.
[3] N. Jalagonia, I. Esartia, T. Tatrishvili, E. Markarashvili, J. Aneli, O. Mukbaniani. Siloxane matrix with methylpropionate side groups and polymer electrolyter membranes on their basis. Oxid. Commun., 39, 2, 1282-1292, 2016;