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In this research, a new method of treating wastewater is introduced using a highly recyclable and sustainable material derived from coconut oil. This material aims to address the issues commonly faced by conventional sorbents, such as limited performance and costly production. These challenges impede a sorbent material from unlocking its full utility in treating wastewater. An exceptional sorbent material was synthesized by incorporating coconut shell-based activated carbon (AC) into a coconut oil-based polyurethane matrix to produce an activated carbon-infused polyurethane (ACIP). The effective adsorption was elucidated by the synergistic interaction between the ACIP material and methylene blue (MB) through electrostatic attraction, π-π interactions, and hydrogen bonding. To provide an exhaustive analysis of the ACIP material, several analytical techniques were employed, including Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) analysis, X-ray diffraction (XRD) analysis, and thermogravimetric analysis (TGA). A detailed assessment using a fixed-bed column setup investigated its adsorption behavior by encompassing various factors such as inlet concentration, adsorbent bed height, feed flow rate, and solution pH. Results revealed that the ACIP composite exhibited a maximum adsorption capacity of 28.25 mg g−1. Empirical evidence with a high correlation coefficient (R2 > 0.93) obtained from the Thomas and Yoon–Nelson model suggests the suitability of the composite material to operate efficiently under these diverse circumstances. Notably, after five consecutive adsorption–desorption cycles, ACIP demonstrated its remarkable reusability by maintaining 86% of its regeneration efficiency. Given its outstanding performance and potential for scalability, this innovative ACIP composite presents a more sustainable approach to addressing wastewater issues within industrial environments. [ABSTRACT FROM AUTHOR]

Polyvinyl chloride (PVC) and polyethylene terephthalate (PET) contribute significantly to global plastic waste, with only 9% recycled in recent years. In this work, these plastic wastes were upcycled as functional fillers to improve the rigid polyurethane foam (RPUF) properties. To attain this target, we leveraged the intrinsic polarity of the C=O and C-Cl groups of PVC and PET to induce intermolecular attractions with the N-H groups of the polyurethane matrix, evidenced by the observed IR peak shifts. This enhanced the nucleating effect during foaming, increasing the foams' compressive strengths by 77% and 22% with the addition of 10% PVC and 5% PET filler, respectively. Furthermore, the addition of PVC and PET fillers increased the foam volume. Thus, the collective utilization of PPW and its corresponding impact on the CO-based RPUF's properties signifies a reduction in carbon dioxide emissions by 14.15% and 17.52% for PVC and PET, respectively. Moreover, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) revealed improved thermal stability and degradation profiles of the produced RPUFs. Overall, this work highlights potential advancement in environmentally responsible upcycling strategies for common end-of-life plastic wastes, while enhancing rigid foam properties. [ABSTRACT FROM AUTHOR]

Soil erosion, a global problem, degrades land quality and increases pollution and sedimentation in bodies of water. This study propounds a new material to mitigate soil erosion using rice straw-based polyurethane foam (RSPF) blocks as a potential replacement for commercially available expanded polystyrene (EPS) foam in slope stabilization. RSPF was synthesized via a conventional one-shot foaming method with 15% rice straw-based polyol content. The RSPF blocks have an average density of 43.29 kg/m3, average compressive strength of 184.55 kPa, closed cell content of 88.4%, and water absorption capacity of 262% that can effectively reduce water runoff. These properties are comparable to EPS foams according to ASTM D6817, except for the high absorption capacity of RSPF. This added feature allows the foam to act as topsoil protection by reducing runoff. In slope stabilization and topsoil protection applications, the effectiveness of the RSPF blocks in reducing soil loss was tested in both simulated and natural rainfall events with different land slope degrees, rain intensities, and soil covers. Results show that the use of RSPF in the simulated setup with a heavy rain intensity of 80 mm/h reduced the soil loss by 61.5%, 22.7%, and 4.3% in 5°, 10°, and 20° of land slope, respectively. There was also a higher degree of soil loss reduction when the RSPF block was coupled with a natural vegetation soil cover by 79.6%, 70%, and 19.3% in 5°, 10°, and 20° land slopes, respectively. Moreover, in the natural rainfall events in an open field with a land slope of 20°, the recorded soil loss reduction reached 93.6–98.8% at an average rainfall intensity of 16.26 mm/h. Additionally, the relationship between soil loss and land slope was investigated to produce a best fit model that predicts the soil loss up to a 20° land slope. An interesting observation was made wherein the erosion rate increased using linear regression modeling in the simulated setup for bare soil (BS), soil with vegetation (SV), soil with RSPF (SF), and soil with RSPF and vegetation (FV), with high coefficient of determination (R2) values between 0.92 and 0.99. These findings suggest that the RSPF block is a promising alternative and sustainable material for EPS foams in mitigating soil erosion, especially under heavy rainfall conditions. [ABSTRACT FROM AUTHOR]

The increasing focus on sustainable construction is driving the industry toward materials that combine functionality with environmental benefits. A viable approach to address this demand is the use of bio-based additives to improve traditional cementitious composites. This study introduces a novel approach to developing a polymer-modified construction material by incorporating varied amounts (0, 1, 2, 3, and 6%) of bio-based polyurethane (PU), derived from polyglycerol polyester polyol, into cementitious mortar. The resulting PU-modified cementitious mortar (PUMC) was evaluated for its mechanical, physicochemical, and microstructural properties. Results show that the incorporation of 2% PU by cement weight significantly enhanced compressive strength by 58.2%, flexural strength by 37.0%, and initial flow performance by 20.0% after 28 days, while a 6% PU incorporation provided the best abrasion resistance. These improvements were attributed to a uniform particle and pore size distribution and the formation of a uniform interpenetrating polymer network (IPN), as confirmed by BET-BJH and SEM-EDX analyses. Additionally, FTIR and TGA analyses revealed that the metal-ligand coordination between Ca 2+ ions in the cement mortar and PU ligand groups strengthened the interfacial connectivity through noncovalent bonding, further enhancing the material properties. This research highlights the potential of bio-based PU as an eco-friendly additive that significantly improves the performance of cementitious mortars, making it a promising option for industrial flooring applications., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

Semiconducting nanoparticles (SNPs) have garnered significant attention for their role in photocatalysis technology, offering a cost-effective and highly efficient method for breaking down organic dyes. Of particular significance within SNP-based photocatalysis are tunable band gap TiO 2 nanoparticles (NPs), which demonstrate remarkable enhancement in photocatalytic efficiency. In the present work, we introduce an approach for the synthesis of TiO 2 NPs using kappa-carrageenan (κ-carrageenan), not just as a reducing and stabilizing agent but as a dopant for the resulting TiO 2 NPs. During the synthesis of TiO 2 NPs in the presence of sulfate-rich carrageenan, the process predominantly leaves residual sulfur and carbon. The presence of residual carbon, in conjunction with sulfur doping, as indicated by fast FTIR spectra, XPS, and EDX, leads to a significant reduction in the band gap of the resulting composite to 2.71 eV. The reduction of composite band gap yields remarkable degradation of methylene blue (99.97%) and methyl orange (97.84%). This work presents an eco-friendly and highly effective solution for the swift removal of environmentally harmful organic dyes., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)