Polyamide is a thermoplastic polymer widely used for several applications, including cables in offshore oil and gas operations. Due to its growing annual production worldwide, this poorly biodegradable material has been a source of pollution. Given this scenario, the need has arisen to develop environmentally friendly techniques to degrade this waste, and biotechnology has emerged as a possible solution to mitigate this problem. This study aimed to investigate the potential of Yarrowia lipolytica to biodepolymerize polyamide fibers (PAF). Microbial cultures were grown in shaken flasks containing different concentrations of PAF (0.5 and 2 g·L⁻¹) and in a bioreactor with and without pH adjustment. PAF mass loss was up to 16.8%, achieved after 96 h of cultivation in a bioreactor without pH adjustment. Additionally, NMR analyses revealed that the amorphous regions of PAF, which are more susceptible to depolymerization, were reduced by 6% during cultivation. These preliminary results indicate the biotechnological potential of Y. lipolytica to depolymerize PAF.

Polyamides (PAs) are widely used as barrier materials in offshore oil and gas (O&G) equipment due to their mechanical strength and chemical resistance. However, long-term exposure to hydrogen sulfide scavengers (H₂S-SCVs) may significantly affect their physicochemical properties. Previous studies using thermal analysis and ¹H time-domain NMR (¹H TD-NMR) suggest that ethoxylated H₂S-SCVs impose molecular constraints, increasing the glass transition temperature (T_g) and reducing chain mobility above T_g. The present study builds upon these findings using a multi-technique analytical approach, including FTIR, Raman, ¹H DQ-TD-NMR, and ¹³C solid-state NMR (ssNMR), to provide a more comprehensive understanding of the molecular alterations in PA materials. The results clearly demonstrate that H₂S-SCV exposure leads to the progressive exudation of plasticizers from the PA matrix. This plasticizer loss is a key factor contributing to the observed shift in Tg and the reduction in molecular mobility. ¹H DQ-TD-NMR data confirmed an increase in the density of dynamically constrained chains over time and allowed for the characterization of heterogeneity in these constraints throughout the PA matrix. Moreover, ¹³C ssNMR spectra revealed the presence of immobilized H₂S-SCV chemical groups within the polymer matrix, strongly supporting the early statement that the mobility constraints observed in ¹H DQ-TD-NMR are associated with the formation of crosslinks induced by the H₂S-SCV: H₂S-SCV acts as a crosslinking agent. Taken together, our findings indicate that both plasticizer loss and H₂S-SCV-induced crosslinking contribute significantly to the microstructural evolution of PAs when exposed to ethoxylated H₂S-SCVs, offering important insights into their degradation mechanisms and long-term behavior in aggressive operational environments.