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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]

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]

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]

Persimmon is among the fruits with a significant postharvest loss over the last few years. Thus, it is important to investigate new technical feasibilities to obtain products with higher added value from this fruit. In this study persimmon puree films (Diospyros kaki L.) incorporated with glycerol and pectin by casting technique were formulated using a Plackett–Burman design and characterized. The puree showed high carbohydrate content (175.70 g/kg). In descending order, fructose, glucose, and maltohexaose were the sugars found in persimmon. All the independent variables studied—puree concentration, pectin, glycerol, and temperature—statistically influenced the tensile strength (0.75–1.30 MPa), elongation at break (17.69–26.02%), and Young's modulus (3.34–10.94 MPa) of the films. Water solubility ranged from 68.80% to 80.86%, which were very similar to other films based on puree fruit in the literature. Samples presented high vapor permeability (5.77–6.63 × 10−6 g/h/m/Pa) when compared to biodegradable films. Scanning electron microscopy showed smooth surfaces and good plasticizer dispersion. The colorimetric coordinates indicated the films are reddish and yellowish, giving them an orange‐ish visual aspect. The films exhibited antimicrobial activity, especially against Escherichia coli and Staphylococcus aureus. These results indicate that the developed films might be a good candidate for antimicrobial food packaging improving food quality and safety. Practical Application: The production of fruit‐film packaging with functional and biodegradable characteristics might reduce postharvest loss of fruit and have the potential to develop active food packaging. In this sense, this study is in line with precepts of the circular economy, once it takes advantage of exceeded resources that would be discarded by generating biodegradable films which can be used as edible packaging. Furthermore, given the antimicrobial potential of the films developed, they might be applied as active packaging to improve food safety and extend shelf life. [ABSTRACT FROM AUTHOR]

Polylactide (PLA) is an eco-friendly biodegradable thermoplastic with excellent processability, demanding less energy to be produced compared to the petroleum-based polymers. However, PLA has drawbacks that impose some restrictions of uses use such as poor toughness property. Blending PLA with other polymers is a more practical and economic way to improve its toughness. The present study assessed the effect of the addition of the pre-crosslinked powdered nitrile rubber (NBR) containing calcium carbonate (CaCO3) and extruder screw rotation on the mechanical, rheological, morphological and thermal properties of polylactide (PLA) by using a Central Composite Rotatable Design (CCRD) analysis, which provides statistical support for the experimental data. The results showed that NBR/CaCO3 can be used as toughness modifier for PLA. This property improved due to the increase in energy expended to deform the material and generate cracks, as showed in the impact and morphological analyzes. Despite this improvement, the presence of CaCO3 caused a slight decline in the thermal resistance of the composites. The influence of rubber (NBR/CaCO3) content in PLA matrix on rheological properties, such as elongation viscosity, melt strength and drawability was also investigated. The results showed that the composition PLA/NBR/CaCO3 with higher NBR/CaCO3 content can be used in thermoforming applications. [ABSTRACT FROM AUTHOR]

This study aimed at evaluating the coupling effect of silane Si69 bis(triethoxysilylpropyl)tetrasulfide in metakaolin (MK) in automobile tire tread compounds based on a styrene–butadiene rubber/butadiene rubber blend. A reference compound of a typical tread recipe, filled with silica and carbon black, was used as a reference due to the acknowledged effect of TESPT in silica incorporation in elastomers. A silica sample without silane was also prepared. Silica was then completely substituted by MK, producing two samples, with and without silane. The samples were tested for crosslink density, rheometry, and morphology, and the vulcanization reaction parameters were determined and evaluated. Silane improved the interaction between MK and the polymer matrix, evidenced by the increase in crosslink density and vulcanization reaction rate, the same effect silane causes on silica-filled composites. Morphology also revealed that silane increased MK dispersion and adhesion to rubber. On the other hand, MK seems not to be as reinforcing as silica, considering that maximum torque is related to the stiffness of the material, with MK exhibiting lower values for this parameter. [ABSTRACT FROM AUTHOR]