The use of biopolymers such as cyclodextrin in textiles for the development of biofunctional fabrics is an alternative for the development of eco-friendly textiles. Cyclodextrins can create covalent interactions with the chemical groups available in wool, allowing the sorption of active molecules that will be released, such as the citronella oil. Therefore, this work investigates the formation of cyclodextrin complex oil applied in wool and its release mechanism. The complexes obtained and the grafted fabric were characterized by TGA, DLS, FTIR-ATR and SEM. The release of citronella oil was also analyzed and mathematical adjustments were performed using the equation of Korsmeyer-Peppas to verify the release mechanism. The results have indicated the formation of the complex and its fixation by covalent bonding, according to the FTIR-ATR specter and the SEM, and these have shown an anomalous release profile. For this reason, the application of the complexes in wool fabrics has shown to be an option in the production of eco-friendly biofunctional materials for controlled release, allowing the oil properties to be used in textile matrices.

No abstract

No abstract

No abstract

Dyes are complex molecules that can sometimes cause damage to the aquatic environment and harm human health. They are often not completely removed from effluent by the usual treatments; therefore, efforts have been made to increase their exhaustion from dyeing through chemical and physical processes. In this context, the use of β-cyclodextrin (β-CD) as dyeing auxiliary agent promotes the reduction of harmful products, also increasing the color intensity of the fabric. In this paper, β-CD was used as a complexing agent to dye polyamide (PA) using the dye C.I. Disperse Yellow 211 (DY211) in order to improve dye exhaustion and color intensity using the β-CD:DY211 complex. The conventional dyeing process and β-CD:DY211 dyeing process by exhaustion were compared, and adsorption kinetics, isotherms, and the coloristic intensity were evaluated. The chemical shifts in the FTIR spectra and the thermal stability evidenced the formation of the β-CD:DY211 complex. Regarding dyeing kinetics and isotherm, the pseudo-first-order model was the most appropriate to describe the process, while Nernst isotherm was the one that best represented the adsorption results. Categorically, the samples dyed with the β-CD:DY211 complex obtained higher coloristic intensity in comparison with the conventional process. With this evidence, it is possible to conclude that cyclodextrin is a suitable replacement for environmentally harmful textile aides without adding further steps into the dyeing process or the need for additional equipment.