The global proliferation of Pinus radiata, known for its rapid growth and wood density, has led to an environmental challenge—significant waste production, especially bark, without a clear valorization route. This waste poses ecological concerns, and despite the crucial role of forest resources in structural applications, their limited fire resistance requires the use of coatings. However, traditional coatings lack an eco-friendly footprint. Addressing this challenge, this study aims to develop an intumescent coating with tannins extracted from waste bark, offering a sustainable alternative. This not only repurposes waste on a global scale but also aligns with the imperative for environmentally friendly materials, contributing to sustainable practices in the construction and wood treatment industry. This study achieved an eco-friendly FRR15 (fire resistance ratio 15) fire resistance classification with a 15% equivalence of low-molecular-weight tannins, presenting a sustainable alternative to commercial products. Characterization showed low-molecular-weight tannins comparable to conventional charring agents, with high hydroxyl content and oil absorption, while high-molecular-weight tannins exhibited lower viability. A reference coating achieved FRR30 fire resistance, aligning with commercial strength. The mechanical properties of tannin-based coatings matched commercial standards, with increased abrasion resistance and adhesion and decreased flexibility. Intumescent coatings with higher tannin content significantly reduced wood substrate charring and mass loss in flame response assessments.

The most commonly used membranes are of the "thin film composite" (TFC) type, consisting of three layers of polymers. Membrane modification has been explored through two main approaches: optimizing the polymer before fabrication or modifying the surface after fabrication. This study focuses on membrane modification by depositing ultrathin films of zinc oxide (ZnO) using the sputtering process. The impact on permeability and monovalent ion rejection is examined. The results show that an increase in ZnO deposition time leads to a reduction in permeate flux density, albeit with an improvement in monovalent ion rejection. The Spielger-Kedem model is demonstrated to effectively predict the behavior of these membranes. Collectively, the findings suggest that membrane modification with ZnO through sputtering can offer significant advantages in water purification applications, albeit with considerations regarding reduced permeate flux density.

Water stress is intensifying worldwide, increasing the need for efficient desalination and water purification technologies. Although commercial nanofiltration membranes such as NF90 exhibit high separation performance, their transport properties remain governed by permeability–selectivity trade-offs, and their surface characteristics offer limited tunability for application-specific requirements. Here, a commercial NF90 polyamide thin-film composite nanofiltration membrane was surface modified by depositing ultrathin ZnO coatings via RF sputtering (30–120 s) and evaluated in terms of surface properties, water permeate flux, and NaCl rejection. X-ray diffraction confirmed the formation of crystalline Wurtzite ZnO with preferential (002) orientation. ZnO deposition markedly increased surface hydrophobicity, raising the water contact angle from 52.5 ± 2.0° for the unmodified membrane to 140.4 ± 3.9° after 120 s of deposition. Hydraulic performance decreased after modification, with water permeate flux reduced by approximately 47–50% relative to pristine NF90. In contrast, NaCl rejection increased with ZnO deposition time, particularly at lower operating pressures, and tended to plateau at higher pressures. The Spiegler–Kedem model accurately described experimental rejection-flux behavior. Overall, RF sputtering of ZnO is a feasible post-fabrication route to tune NF membrane selectivity, while introducing a clear trade-off with permeate flux.