This experimental study is associated with the modification of glass fibers with efficient, organic, functional, thermoelectrically enabled coatings. The thermoelectric (TE) behavior of the coated glass fiber tows with either inherent p semiconductor type single wall carbon nanotubes (SWCNTs) or the n-type molecular doped SWCNTs were examined within epoxy resin matrix in detail. The corresponding morphological, thermogravimetric, spectroscopic, and thermoelectric measurements were assessed in order to characterize the produced functional interphases. For the p-type model composites, the Seebeck coefficient was +16.2 μV/K which corresponds to a power factor of 0.02 μW/m∙K2 and for the n-type −28.4 μV/K which corresponds to power factor of 0.12 μW/m∙K2. The p–n junction between the model composites allowed for the fabrication of a single pair thermoelectric element generator (TEG) demonstrator. Furthermore, the stress transfer at the interphase of the coated glass fibers was studied by tow pull-out tests. The reference glass fiber tows presented the highest interfacial shear stress (IFSS) of 42.8 MPa in comparison to the p- and n-type SWCNT coated GF model composites that exhibited reduced IFSS values by 10.1% and 28.1%, respectively.
The present study demonstrates, for the first time, the ability of a 10-ply glass fiber-reinforced polymer composite laminate to operate as a structural through-thickness thermoelectric generator. For this purpose, inorganic tellurium nanowires were mixed with single-wall carbon nanotubes in a wet chemical approach, capable of resulting in a flexible p-type thermoelectric material with a power factor value of 58.88 μW/m·K2. This material was used to prepare an aqueous thermoelectric ink, which was then deposited onto a glass fiber substrate via a simple dip-coating process. The coated glass fiber ply was laminated as top lamina with uncoated glass fiber plies underneath to manufacture a thermoelectric composite capable of generating 54.22 nW power output at a through-thickness temperature difference οf 100 K. The mechanical properties of the proposed through-thickness thermoelectric laminate were tested and compared with those of the plain laminates. A minor reduction of approximately 11.5% was displayed in both the flexural modulus and strength after the integration of the thermoelectric ply. Spectroscopic and morphological analyses were also employed to characterize the obtained thermoelectric nanomaterials and the respective coated glass fiber ply.
In the present research work is demonstrated a cross-scale manufacturing approach for the production of multifunctional glass fiber reinforced polymer (GFRP) composite tubes with a purposely redesigned filament winding process. Up until now, limited studies have been reported towards the multiscale reinforcement direction of continuous fibers for the manufacturing of hierarchical composites at the industrial level. This study involved the development of two different multi-walled carbon nanotube (MWCNT) aqueous-based inks, which were employed for the modification of commercial glass fiber (GF) reinforcing tows via a bath coating unit in a pilot production line. The obtained multifunctional GFRP tubes presented a variety of characteristics in relation to their final mechanical, hydrothermal aging, electrical, thermal and thermoelectric properties. Results revealed that the two individual systems exhibited pronounced differences both in crushing behavior and durability performance. Interestingly, for lateral compression the MWCNT coatings comprising a polymeric dispersant minorly affected the mechanical response of the produced tubes. The crashworthiness indicators of the multifunctional tubes displayed a slight 5% variation to the respective reference values, combined with a more ductile behavior. Moreover, regarding the bulk electrical and thermal conductivity values, as well as the Seebeck coefficient factor, the corresponding tubes displayed a variance of 233% and 19% and an opposite semi-conducting sign denoting a p- and n-type character, respectively.