Multiwall carbon nanotubes (MWCNTs) oxidized by an acid treatment were deposited on the surface of as-received commercial aramid fibers containing a surface coating ("sizing"), and fibers modified by either a chlorosulfonic treatment or a mixture of nitric and sulfuric acids. The surface of the aramid fiber activated by the chemical treatments presents increasing density of CO, COOH and OH functional groups. However, these chemical treatments reduced the tensile mechanical properties of the fibers, especially when the nitric and sulfuric acid mixture was used. Characterization of the MWCNTs deposited on the fiber surface was conducted by scanning electron microscopy, Raman spectroscopy mapping and X-ray photoelectron spectroscopy. These characterizations showed higher areal concentration and more homogeneous distribution of MWCNTs over the aramid fibers for as-received fibers and for those modified with chlorosulfonic acid, suggesting the existence of interaction between the oxidized MWCNTs and the fiber coating. The electrical resistance of the MWCNT-modified aramid yarns comprising 1000 individual fibers was in the order of M Omega/cm, which renders multifunctional properties.CONACYT-CIAM (Mexico) 188089 CONICYT (Chile) 120003 "Fondo Mixto CONACYT-Gobierno del Estado de Yucatan" 24704

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Curing effects were investigated by using the electrical response of a single carbon nanotube yarn (CNTY) embedded in an epoxy resin during the polymerization process. Two epoxy resins of different viscosities and curing temperatures were investigated, varying also the concentration of the curing agent. It is shown that the kinetics of resin curing can be followed by using the electrical response of an individual CNTY embedded in the resin. The electrical resistance of an embedded CNTY increased (~9%) after resin curing for an epoxy resin cured at 130 °C with viscosity of ~59 cP at the pouring/curing temperature (“Epon 862”), while it decreased (~ −9%) for a different epoxy cured at 60 °C, whose viscosity is about double at the corresponding curing temperature. Lowering the curing temperature from 60 °C to room temperature caused slower and smoother changes of electrical resistance over time and smaller (positive) residual resistance. Increasing the concentration of the curing agent caused a faster curing kinetics and, consequently, more abrupt changes of electrical resistance over time, with negative residual electrical resistance. Therefore, the resin viscosity and curing kinetics play a paramount role in the CNTY wicking, wetting and resin infiltration processes, which ultimately govern the electrical response of the CNTY immersed into epoxy.

Carbon nanotube yarns (CNTYs) are hierarchical fibers with outstanding electrical properties, and understating the temperature‐dependence of their electrical resistance (thermoresistivity) is essential for sensing applications and development of self‐sensing polymer composites. The cyclic thermoresistive response of individual CNTYs and the effect of embedding the yarn into a polymer are experimentally investigated herein. The effect of confining the CNTY by a thermosetting polymer is addressed by studying the thermoresistive response of CNTY/vinyl ester single‐fiber composites. Heating–cooling cycles ranging from 25 (room temperature [RT]) to 100 °C and 25 to −30 °C are applied to individual CNTYs and to CNTYs embedded into a vinyl ester polymer, while their electrical resistance is simultaneously recorded. Both the CNTY and its single‐fiber composite show a negative dependence of electrical resistance with temperature. For both temperature ranges (above and below RT), the average temperature coefficient of resistance found for individual CNTYs is ≈−9.5 × 10−4 K−1, and its magnitude decreases about ≈30% when the yarn is embedded into the vinyl ester polymer. The hysteresis rendered by the different heating and cooling pathways is small for individual CNTYs, and largely increases when the CNTY is embedded into the polymer.