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The application of electrocatalysts used at high cathodic overpotentials for the electrochemical reduction of pollutant species such as CO 2 has revealed a lack of understanding of the cathodic degradation mechanisms of those materials. Pure Sn is one of the most relevant candidate materials mainly because of its high selectivity for the reduction of CO 2 to formic acid and formate salts. Degradation of the electrocatalyst can arise from a combination of cathodic polarization and induced changes to the surface by CO 2 reduction products. In this study, the cathodic degradation mechanisms of pure Sn were studied as a function of rotation rate, time, current density, electrolyte concentration, grain size, and orientation in a nitrogen-saturated atmosphere using a rotating disk electrode. Several degradation morphologies were observed, but three were dominant. In the first type, electrochemical alterations of grains with specific orientations produced substantial weight changes, both losses and gains. The second type resulted in an alkali-rich deposit that had a high coverage but produced small weight changes. The third type consisted of carbon-rich stains that typically had a small coverage.

Bacterial nanocellulose (BNC) was used to synthesize polyurethane foams (PUFs) prepared from castor oil polyol and MDI diisocyanate using water as the blowing agent. The BNC reacted with the isocyanate, increasing the weight content of urethane hard segments (HS). It did not behave as a nucleation agent, forming a nanometric distribution of cells within the struts followed by a reduction of the apparent density (−7.6%) and a relevant increase of cell size in the growth direction (+37.9%). An alignment of the BNC parallel to the cell walls was observed, producing a nanocomposite with a higher reinforcement weight fraction in that area. At only 0.2 wt %, the BNC behaved as a nanostructured reinforcement, improving the specific compression modulus and strength by +4.67% and +23.6%, respectively, as well as the thermomechanical properties, with an improvement of the specific E′ at 30 °C of +52.4%. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 44982.

A systematic investigation of four processing routes was implemented so as to evaluate the thermal and mechanical properties of nanosilica (NS) reinforced poly(urethane‐isocyanurate) nanocomposites (NC). The NS dispersion in the Polmix and the Isomix routes was performed in the polyol and the isocyanate precursor, respectively. The Isopol and the Solvmix routes consisted on the dispersion of the filler after the mixing of the precursors and with the aid of solvents, respectively. The NS dispersion, fractography (SEM, TEM), flexural and tensile mechanical properties, thermogravimetric analysis and FTIR analysis of NCs was performed as a function of processing route, isocyanate index, and NS concentration. Each route produced a NC with distinct properties, which were correlated to the NS agglomeration degree and how the NS affected the thermal transitions of the HS and the relative ratio of urethane and isocyanurate chemical groups. For example, the NC prepared with the Polmix route had substantial improvements of σt and εt of around +40 and +52%, respectively and an improved thermal resistance of the Hard Segments. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 42750.

Nanocellulose reinforced foams are lightweight with improved mechanical properties; however, the strain‐rate effect on their mechanical response is not yet fully understood. In this work, rigid polyurethane foams (PUFs) nanostructured with bacterial nanocellulose at 0.2 wt % (BNCF) and without it (PUF) are synthesized and subjected to compression tests at different strain rates. The BNC acts as a nucleation agent, reducing the cell size but maintaining a similar apparent density of 40.4 ± 3.3 kg m−3. Both BNCF and PUF exhibit strain‐rate effect on yield stress and densification strain. The BNCF exhibits localized progressive crushing and reduced friability, causing a remarkable recovery in the transverse direction. Numerical simulations show that functionally graded foams subjected to impact could be designed using different layers of PUF and BNCF to vary energy absorption and acceleration rate. The results presented herein warrant further research of the mechanical properties of nanostructured foams for impact applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 137, 48701.

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We synthesized polyols with high hydroxyl functionalities (F OH s), between 9.0 and 12.6, and characterized them with differential scanning calorimetry, thermogravimetric analysis, and size exclusion chromatography after we parametrically studied the ringopening reaction of epoxidized soybean oil with lactic acid (LA) as a function of the reaction temperature and lactic acid equivalent fraction (f LA ). An increase of only 20 C in the reaction temperature (from 80 to 100 C) caused changes in the hydroxyl number (+17.8%), F OH (-25%), viscosity (-14.0%), and oligomeric content (-24.1%). f LA mostly affected the ring-opening yield, and only for f LA values above 0.4 was possible to achieve values higher than 80%. Rigid polyurethane foams (rPUFs) were synthesized and characterized with scanning electron microscopy, dynamic mechanical analysis (DMA), and compressive mechanical tests. rPUFs with a very high specific compressive strength (7.8 kPa kg -1 m 3 ) were synthesized solely with biobased soybean oil. DMA revealed a compromised relationship between the specific compressive strength and its temperature dependence. To increase the first one, the most relevant method was to increase F OH . Instead, to increase the latter one, the OH number had to be maximized.