Silver Nanowires and Silanes in Hybrid Functionalization of Aramid Fabrics.

New functionalization methods of meta- and para-aramid fabrics with silver nanowires (AgNWs) and two silanes (3-aminopropyltriethoxysilane (APTES)) and diethoxydimethylsilane (DEDMS) were developed: a one-step method (mixture) with AgNWs dispersed in the silane mixture and a two-step method (layer-by-layer) in which the silanes mixture was applied to the previously deposited AgNWs layer. The fabrics were pre-treated in a low-pressure air radio frequency (RF) plasma and subsequently coated with polydopamine. The modified fabrics acquired hydrophobic properties (contact angle ΘW of 112-125°). The surface free energy for both modified fabrics was approximately 29 mJ/m2, while for reference, meta- and para-aramid fabrics have a free energy of 53 mJ/m2 and 40 mJ/m2, respectively. The electrical surface resistance (Rs) was on the order of 102 Ω and 104 Ω for the two-step and one-step method, respectively. The electrical volume resistance (Rv) for both modified fabrics was on the order of 102 Ω. After UV irradiation, the Rs did not change for the two-step method, and for the one-step method, it increased to the order of 1010 Ω. The specific strength values were higher by 71% and 63% for the meta-aramid fabric and by 102% and 110% for the para-aramid fabric for the two-step and one-step method, respectively, compared to the unmodified fabrics after UV radiation.

Effect of Reactive Dyeing on Fabrics Modification with Silver Nanowires (AgNWs).

This paper presents the characterization of cotton and wool fabrics modified by silver nanowires (AgNWs). The effect of reactive dyeing of wool and cotton fabrics on their modification with AgNWs was analyzed. Both fabrics were dyed using reactive dyes (yellow, red, blue) at four color intensities (0.5, 1, 2, and 5%). Dyed fabrics were characterized by the determined Kubelka-Munk's coefficient (K/S) ratio and vibrational spectra (Fourier transform infrared (FTIR) and Raman). Analysis of the amount of AgNWs applied on cotton and wool fabrics indicates that the presence of dye affects the surface modification with AgNWs depending on the type of fibers. While for cotton no significant differences were noted in relation to the color intensity, in the case of wool, the higher the dye contents, the more nanowires were deposited on the surface. Surface-enhanced Raman spectroscopy (SERS) effect accompanying AgNW modification was also observed on wool, similar to the previous study on cotton.

A SnO2 shell for high environmental stability of Ag nanowires applied for thermal management.

Since silver nanowires (AgNWs) show high infrared reflectance many studies present their applicability as thermal management products for various wearable textiles. However, their use for practical purposes is only partially evaluated, without focusing on improving their low atmospheric and liquid stability. This report describes a new approach for the topic and proposes a facile method of Ag nanowire passivation with a SnO2 layer for high environmental stability and retention of high infrared reflectance. The one-step passivation process of AgNWs was carried out in the presence of sodium stannate in an aqueous solution at 100 °C, and resulted in the formation of core/shell Ag/SnO2 nanowires. This study presents the morphological, chemical, and structural properties of Ag/SnO2NWs formed with a 14 nm thick SnO2 shell, consisting of 7 nm rutile-type crystals, covering the silver metallic core. The optical properties of the AgNWs changed significantly after shell formation, and the longitudinal and transverse modes in the surface plasmon resonance spectrum were red shifted as a result of the surrounding media dielectric constant changes. The passivation process protected the AgNWs from decomposition in air for over 4 months, and from dissolution in a KCN solution at concentrations up to 0.1 wt%. Moreover, the report shows the microwave irradiation effect on the shell synthesis and previously synthesised Ag/SnO2NWs. The post-synthesis irradiation, as well as the SnO2 shell obtained by microwave assistance, did not allow long-term stability to be achieved. The microwave-assisted synthesis process was also not fast enough to inhibit the formation of prismatic silver structures from the nanowires. The Ag/SnO2NWs with a shell obtained by a simple hydrolysis process, apart from showing high infra-red reflectance on the para-aramid fabric, are highly environmentally stable. The presented SnO2 shell preparation method can protect the AgNW's surface from dissolution or decomposition and facilitate the designing of durable smart wearable thermal materials for various conditions.

Influence of Low-Pressure RF Plasma Treatment on Aramid Yarns Properties.

The aim of the study was to modify the surface free energy (SFE) of meta- (mAr) and para-aramid (pAr) yarns by their activation in low-pressure air radio frequency (RF) (40 kHz) plasma and assessment of its impact on the properties of the yarns. After 10 and 90 min of activation, the SFE value increased, respectively, by 14% and 37% for mAr, and by 10% and 37% for pAr. The value of the polar component increased, respectively by 22% and 57% for mAr and 20% and 62% for pAr. The value of the dispersion component for mAr and pAr increased respectively by 9% and 25%. The weight loss decreased from 49% to 46% for mAr and 62% to 50% for pAr after 90 min of activation. After 90 min, the specific strength for mAr did not change and for pAr it decreased by 40%. For both yarns, the 10 min activation in plasma is sufficient to prepare their surface for planned nanomodification.

Assessment of Thermal Performance of Textile Materials Modified with PCM Microcapsules Using Combination of DSC and Infrared Thermography Methods.

The aim of the study was the combination of two measurement methods, the differential scanning calorimetry (DSC) and infrared thermography to evaluate thermal performance of woven and knitted fabrics coated with acrylic pastes containing 20% (P/20) and 40% (P/40) of microcapsules of phase change materials (MPCM) with transition temperatures of 28 °C (MPCM28) and 43 °C (MPCM43). The DSC analysis showed that the phase transition processes for materials modified with pastes P/20 occur in a narrower temperature range than those modified with P/40 pastes. The initial temperatures TOnset (S-S) and TOnset (S-L) are higher for materials modified respectively with pastes P/20 and P/40. The melting and crystallization enthalpy values of both P/20 coated materials are lower by about 45% and 35% compared to P/40. Infrared thermography analysis showed that materials modified with P/20 are heating up faster than modified with P/40 for both MPCM. In the cooling process for modified fabrics the highest temperature decrease was observed in the first 30s. Materials modified with paste P/40 were cooled more slowly in comparison with paste P/20, both for MPCM28 and MPCM43.