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Fluoroelastomers (FKM) are used to manufacture seals and other rubber devices that can withstand harsh operating conditions, including aggressive media and extreme low and high temperatures. Even though nuclear magnetic resonance, Fourier-transform infrared spectroscopy (FTIR), and chromatographic techniques have been extensively used in the characterization of raw FKM molecules, the identification of cured compounds entails a characterization method that is able to overcome the complexity related to this kind of structure. In this sense, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy can outperform other characterization techniques because it does not require solubilization or any special preparation of the sample. In this study, 10 FKM compounds were produced in this study utilizing four commercial types of FKM and the fillers carbon black, barium sulfate, and iron oxide. All unfilled-FKM (as received) and their compounds were analyzed by ATR-FTIR with germanium crystal. Between 15 and 25 analyses were performed for all each FKM type sample and their respective compounds. All spectra were analyzed, and the bands were assigned. Findings regarding the interference of the fillers in the spectra were also reported. From relationships between the height of the spectral zones and the bands at 1397 and 1428 cm−1, it was possible to distinguish all sample compositions of FKM types 1, 2, 3, and 5. This study demonstrates that ATR-FTIR has the potential to be utilized as a technique to detect the type of FKM compounds, an important rubber used in harsh industrial applications. Replacing carbon with BaSO4 reduces the tensile at 50% strain of FKM types 1 and 2 composites. FKM types 3 and 5 composites filled with 30 phr of carbon black have a higher tensile at 50% strain than those of FKM type 1. [ABSTRACT FROM AUTHOR]

In this work, novel nanocomposite films based on babassu coconut mesocarp and zinc oxide nanoparticles (ZnO NPs), synthesized by a green route, were produced for application as food packaging films. The films were prepared using the casting method containing different contents of ZnO NPs (0 wt%, 0.1 wt%, 0.5 wt%, and 1.0 wt%). The films were characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), instrumental color analysis, and optical properties. The water vapor permeability (WVP) and tensile strength of films were also determined. The antimicrobial activity of the films against cooked turkey ham samples contaminated with Staphylococcus aureus was investigated. The results showed that incorporating ZnO NPs into babassu mesocarp matrices influenced the structure of the biopolymer chains and the color of the films. The BM/ZnO-0.5 film (0.5 wt% ZnO NPs) showed better thermal, mechanical, and WVP properties. Furthermore, the synergistic effect of babassu mesocarp and ZnO NPs in the BM/ZnO-0.5 film improved the antimicrobial properties of the material, reducing the microbial count of S. aureus in cooked turkey ham samples stored under refrigeration for 7 days. Thus, the films produced in this study showed promising antimicrobial packaging materials for processed foods. [ABSTRACT FROM AUTHOR]

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This study produced and characterized composites based on nitrile rubber reinforced with rockwool fiber (RW) and carbon black (CB). Ten formulations with dual‐filler loading amounts ranging from 0 to 40 phr of CB and RW were designed using a simplex‐centroid mixture. The composites were assessed regarding their rheometric, rheological, mechanical, and thermal properties. The use of the RW in the dual‐filler system contributed to overall improvements in Shore A hardness, tear strength, modulus at 50%, and resilience, as well as reducing the Payne effect. Instead of using 40 phr of CB alone, a dual‐filler system comprising 20 phr of CB and 20 phr of RW lowers the Payne effect by around 60%, improves resilience by 35%, modulus at 50% strain by 8%, and the residual stress at equilibrium (σ∞/σ0) by 7%. On the other hand, the tensile strength is reduced by 23%. The optimum cure time, crosslink density, and maximum decomposition rate temperature were not affected by the rockwool's presence in the dual‐filler system. In general, the use of RW in combination with CB is advantageous mainly because it reduces compressive stress relaxation, which is an important property for sealing applications. Highlights: Dual‐filler systems based on carbon black (CB) and rockwool fiber (RW) offer advantages.RW‐rich dual‐filler systems reduce stress relaxation.RW‐rich dual‐filler systems reduce the Payne effect.CB‐rich dual‐filler systems increase tensile strength. [ABSTRACT FROM AUTHOR]

The paper and pulp industry produces lignin as a byproduct, which could be a bio‐based reinforcing filler for rubber. Carboxylated nitrile rubber (XNBR) contains carboxyl groups that form ionic bonds with zinc oxide, potentially increasing compatibility with lignin, compared to usual nonpolar rubbers. This study employed the traditional mixing method, two‐roll mill, to incorporate hardwood Kraft lignin without chemical or physical modification as a reinforcing filler in commercial XNBR. A mixture design of experiments was used to explore the effect on rubber/lignin interaction of the carboxyl group content (from 1% to 7% in blends of XNBR) and the amount of lignin (from 0 to 40 phr). Adding 40 phr of lignin increased stress at 100% in XNBR 7% from 1.7 to 6.3 MPa. In XNBR 1%, the increase was from 1.2 to 1.9 MPa. Lignin showed better interaction and dispersion with XNBR 7%, determined from response surface of G′ at high deformations and SEM, respectively. Loss of thermal transition in DMA indicates interaction through ionic groups. These results show that the presence of carboxyl groups enhances the rubber/lignin interaction. This research open possibilities of compatibilization of lignin, offering guidance for future studies and technologies involving lignin in technical applications. Highlights: Lignin dispersion increased as the carboxyl group content increased to 7% (w/w).Stress at 100% elongation increased 370% with 40 phr of lignin and 7% carboxyl.Rubber/lignin interaction as per G′ increased with carboxyl groups.Loss of thermal transition suggests lignin/carboxy/zinc oxide interaction.Lignin can be used as a reinforcing filler in nitrile carboxylated rubber. [ABSTRACT FROM AUTHOR]

Zinc oxide (ZnO) is the most widely used activator in the rubber industry; however, there is growing concern about its use as it can become toxic to the environment, particularly in aquatic systems. This study describes the synthesis of magnesium oxide (MgO) assisted by the Alpinia zerumbet extract, which is then used as an activator in the replacement of ZnO to vulcanize nitrile rubber (NBR) containing 33% and 45% acrylonitrile (ACN). The t90 for NBR‐33% and NBR‐45% are 20 and 15 min, respectively. This indicates a reduction of 5 min in t90 with an increase in ACN. In comparison, ZnO‐activated NBR compounds exhibit the opposite trend, with t90 increasing from 10 for NBR‐33% to 19 min for NBR‐45%. Furthermore, the decrease in activation energy (Ea) with the increase in conversion for 33%‐MgO and 45%‐MgO indicates that vulcanization with MgO is a complex process. This behavior is comparable to that of 45%‐ZnO, but not for 33%‐ZnO because its Ea remains oscillating at 80–90 kJ mol−1 in the entire conversion range. The crosslink densities of 33%‐MgO and 45%‐MgO are 5.87 and 4.78 mol cm−3, respectively. These values are slightly higher than those for 33%‐ZnO (5.77 mol cm−3) and 45%‐ZnO (4.38 mol cm−3). [ABSTRACT FROM AUTHOR]

In this work, the stability of oil-in-water emulsions (O/W) of patauá (Oenocarpus bataua) and pracaxi (Pentaclethra macroloba) oils, both from Amazon rainforest, was investigated. Low-energy emulsification methods were used, such as Emulsion Inversion Point (EIP) and Phase Inversion Temperature (PIT), both based on the minimal interfacial surface, combined with optimized Hydrophilic-Lipophilic Balance (HLB). Phase inversion was determined by electrical conductivity measurements. The surfactants used were Span® 80, Tween® 20, Tween® 60, and Tween® 80. Surfactant mixtures of Span® 80 + Tween® 80 were the best samples prepared. The composition of the most stable samples was 80.00 wt% aqueous phase, 15.00 wt% nonionic surfactants, and 5.00 wt% oil phase (patauá or pracaxi oil). The samples with the best kinetic results were those prepared with the required HLB and PIT values of 12.86 and 84.05 °C, for patauá oil, and of 9.61 and 79.50 °C for pracaxi oil. The kinetic stability of the oil emulsions was characterized by creaming index (CI), by evolution over time of the droplet size, viscosity, and electric conductivity. The results showed that: (1) the droplet size distribution influenced electric conductivity; (2) the relative amount of surfactants Tween® and Span® used is more important to determine the physicochemical and interfacial properties of the emulsion than the oil identity itself; (3) it is crucial to pay attention to the influence of air bubbles—involuntarily inserted into the mixture during the emulsification process—in the physicochemical properties of the system. These conclusions can be extended to other oil-in-water emulsions. [ABSTRACT FROM AUTHOR]

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Copyright of Revista de Direitos Fundamentais & Democracia is the property of Revista de Direitos Fundamentais & Democracia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)