Antibacterial LDPE Nanocomposites Based on Zinc Oxide Nanoparticles/Vermiculite Nanofiller

Polyethylene (PE) nanocomposites with the zinc oxide-nanoparticles/vermiculite nanofiller were prepared in two-steps. In first step, the ZnO-np/V nanofiller were prepared by the mechanochemical method followed by a heat treatment at 650?°C for 90 min. In second step, this nanofiller was used in concentration 3, 6, 10 and 15 wt% for PE nanocomposites preparation via melt compounding technique, the nanocomposites plates were pressed. The particles morphology of the ZnO-np/V nanofiller, arrangement of the ZnO-np/V nanofiller and surface of the PE plates were studied using scanning electron microscopy, optical light microscopy and atomic force microscopy. The surface roughness of the PE plates was evaluated from AFM measurements. Structural changes of the ZnO-np/V nanofiller in PE nanocomposites were monitored using X-ray diffraction analysis and Fourier transform infrared analysis. The gradual and long-term antibacterial effect of PE nanocomposites was tested on the Gram positive bacteria E. faecalis by counting the colony forming units number.     

Effect of the drying process on the compressive strength and cell proliferation of hydroxyapatite‐derived scaffolds

The compressive strength and MC3T3 cell proliferation response of robocast hydroxyapatite‐derived scaffolds was evaluated for samples fabricated by conventional and freeze‐drying methods followed by sintering at 1100 or 1300°C. Both the sintering temperature and, especially, the drying method affected significantly the size and morphology of the residual microporosity within the robocast scaffold's struts. The freeze‐drying method generated a persistent large (1‐10 μm) microporosity of dendritic morphology that was found to improve the biological response of hydroxyapatite‐derived scaffolds. Conversely, conventional drying enhances the compressive strength of the structures. Strength was also increased at the higher sintering temperature, although at the expense of a poorer cell proliferation behavior. The results of this study suggest that the use of a freeze drying process after printing by robocasting provides a very appropriate method for enhancing the biological performance and reliability of bioceramic robocast scaffolds without severely reducing their compressive strength. And, thus, shows promise as an effective method to optimize the performance of robocast scaffolds for bone tissue regeneration.     

Deactivation of CuZn Catalysts Used in Glycerol Hydrogenolysis to Obtain 1,2-Propanediol

Different CuZn catalysts were prepared by coprecipitation method with Cu/Zn atomic ratio of 0.2, 0.4, 1.0, 2.5 and 6.0. Monometallic Zn and Cu catalysts and a bimetallic catalyst (Cu/Zn?=?2.5) prepared by physical mixture of the precursors were also studied. These catalysts were tested in the glycerol hydrogenolysis reaction and the higher yields to 1,2-propanediol were achieved for Cu/Zn atomic ratio?≥?1 samples. The deactivation of a representative catalyst (Cu/Zn?=?1) was evaluated and its yield to 1,2 propanediol decreases until ca 40% after five runs. To explain this behavior, fresh and used catalysts were characterized by different techniques. Chemical analysis of solid catalysts and liquid reaction medium confirmed the leaching of Zn species under our reaction conditions. This process promotes Cu sintering which is proposed as the actual reason of the observed deactivation in the glycerol hydrogenolysis for this catalytic system.     

Impact of particle morphology on structure,crystallization kinetics,and properties of PCL composites with TiO<Subscript>2</Subscript>-based particles

Crystallization kinetics of polycaprolactone (PCL) filled with TiO₂-based particles (TiX) was shown to depend on the TiX particle type and concentration, which were associated with a slight polymer matrix degradation. The partially degraded, shorter, and more mobile polymer chains increased the overall crystallization rate at the initial stage of crystallization, while at the later stages, the non-nucleating TiX particles acted as a sterical hindrance, slowing down the crystallization process. The PCL/TiX composites were prepared by melt-mixing and contained 2.5 and 5 wt% of the filler. The investigated TiX particles included isometric anatase microparticles (mTiO₂) and titanate nanotubes with high-aspect ratio (TiNT). Light and electron microscopy showed very homogeneous dispersion of the mTiO₂ particles in the PCL matrix, while the TiNT formed large agglomerates. In situ polarized light microscopy displayed faster isothermal crystallization of all PCL/TiX composites, but the micrographs indicated that the TiX particles did not act as nucleation centres. Isothermal DSC experiments, evaluated in terms of Avrami theory, confirmed the PLM results and showed that the overall rate of isothermal crystallization increased in the following order: PCL <PCL/TiNT <PCL/mTiO₂. Non-isothermal DSC and rheological measurements revealed the correlation between the crystallization rate and the polymer matrix degradation—the well-dispersed mTiO₂ particles with high specific surface caused the highest PCL degradation and, consequently, the earliest start of non-isothermal crystallization as well as the fastest isothermal crystallization. Microindentation hardness measurements confirmed that the partial degradation of the polymer matrix did not have a significant impact on the mechanical performance of PCL/mTiO₂ composites.     

Structure and morphology of plasma polyfuran particles

A study about the chemical structure, morphology and electric conductivity of polyfuran spherical particles synthesized by rf plasma glow discharges is presented in this work. This kind of particles is difficult to obtain with other syntheses at lower energy. The particles had average diameter that increased linearly with the energy of synthesis, from 172 to 456 nm with 2.91 nm/W growth rate. The chemical structure of the particles was analyzed by XPS relating the formation energy of the polymeric chemical groups with their C1s and O1s atomic orbital energies. The analysis indicated that almost all alpha C configurations of the initial furan molecules transformed into unions of monomers to construct linear polymers. On the other hand, almost all beta configurations remained unreacted in the furan rings and those that reacted transformed into the networked unions of the polymeric structure, approximately 10 %. The percentages of fragmentation, hydrogenation and resonance groups in the structure were also calculated. The particles thermally degraded in one phase from 200 to 600 °C, centered at 425 °C, suggesting that all synthesized particles have similar structure. The electric conductivity of the particles was between 10^?11 and 10^?09 S/m, increasing with the temperature, in which it is probable that the contact resistance among particles rule the transference of charges. The electronic activation energy was in the interval of semiconductors, from 0.031 to 3.83 eV.     

Photo-fenton and UV photo degradation of naphthalene with zero- and two-valent iron in the presence of persulfate

An initial set of 12 kinetic experiments was carried out to remove naphthalene from an aqueous effluent by photo-Fenton involving Fe⁰ and Fe²⁺ at two different concentrations of H₂O₂ (150 and 300?mg?L^?1) and three different pHs (3, 5, and 7) (2²×3¹ experiments). The rate constants (k) for the reaction of naphthalene degradation by involving Fe²⁺ as reactant were in general higher than those with Fe⁰, but the use of Fe²⁺ increased the concentration of naphthalene at equilibrium (C_e) when compared with the same response obtained with Fe⁰ at analogous conditions. A second set of twelve kinetic experiments of photo-Fenton degradation was also performed with persulfate as additive at the conditions already reported, but at a constant concentration of H₂O₂ of 150?mg?L^?1 (2¹×3¹ experiments with NaCl +2¹×3¹ experiments without NaCl). In almost all the runs in which only the source of iron was varied, k from the kinetic data involving Fe²⁺ was higher than that involving Fe⁰, but no difference was observed in terms of C_e that was always zero. The addition of persulfate to treat the effluent either containing or not containing salt enhanced the chemical kinetics, and shifted the equilibrium toward the full removal of naphthalene. A final set of nine experiments of UV photo degradation of naphthalene by involving persulfate without iron, with Fe⁰ and Fe²⁺ in the pH range from 3 to 7 (3² experiments) mainly showed that the use of H₂O₂ may be avoided to remove rapidly and completely naphthalene from wastewater.     

Preparation and characterization of a macroporous agarose monolith as a stationary phase in IMAC chromatography

A macroporous monolith used as stationary phase for the separation of biomolecules by immobilized metal ion affinity chromatography (IMAC), based on D5 agarose (D5) chemically modified was proposed. The characterization of physical properties was studied. Pressure drop was <0.4?MPa, being a very low value compared to other similar chromatographic supports. The adsorption/desorption process was carried out using bovine serum albumin (BSA) at pH 7.4 as a target protein. The monolith was re-used for 20 adsorption/desorption cycles and it was possible to verify that the average percentage of adsorption in all cycles was 89.65%. It was also possible to apply a model in order to obtain the kinetic adsorption constant (k_a), desorption constant (k_d) and equilibrium constant (K_e) by the proposed system. These results indicate that this system is governed by the adsorption process.     

Modeling the effect of a superabsorbent polymer material as desiccant in maize drying using CFD

Maize is an important foodstuff in many countries, and one of most susceptible crops to mold and aflatoxin contamination, which results in considerable postharvest losses and is a burden to consumers’ health, especially in developing countries. The timely drying of harvested maize is essential to halt mold development, ensuring safe storage. The effect of the incorporation of a superabsorbent polymer (SAP) as desiccant in a maize dryer was studied using computational fluid dynamics simulations which accounted for heat and mass transfer between maize, SAP and air. The adsorption capacity and adsorption rate of a commercial SAP material were experimentally determined at different temperature and relative humidity levels, which served as basis for the adsorption model required in the simulations. A maize bulk with SAP packages distributed in it was modeled. Results showed that the SAP material increases the drying rate substantially, particularly in the upper bulk zone where the air reaching it is dehumidified the most. The maize closer to the upper bulk surface starts drying from the beginning of the process instead of lagging for hours or days before the drying front reaches it. An inconvenience of the SAP material is the tendency of granules to swell and stick together as moisture reaches a threshold, which may reduce its performance. Thus, provided this issue is resolved or minimized, SAP materials could successfully assist the rapid drying of maize and other crops. They may also be used during storage to avoid rewetting of the crops during periods of high relative humidity.     

Magnetoelectric coupling in multiferroic BiFeO3 by co-doping with strontium and nickel

We report the effects of the Sr²⁺ and Ni²⁺ co-doping of BiFeO₃ on the crystal structure and multiferroic properties of Bi_1?xSr_xFe_1-yNi_yO₃ (x?=?0.05, 0.0?≤?y?≤?0.10, and Δy?=?0.05) that is synthesized using assisted high-energy ball milling. The mixtures of Bi₂O₃, Fe₂O₃, SrO and NiO were milled for 5?h, pressed at 900?MPa, and sintered at 800?°C in order to obtain cylindrical test pieces. X-ray diffraction and Rietveld refinement elucidated the effects of Sr²⁺ and Ni²⁺ on the crystal structure. Co-doping with SrNi in suitable proportions stabilizes rhombohedral BiFeO₃. High contents of Ni²⁺ promote the precipitation of secondary phases in the forms of NiFe₂O₄ and Bi₂₅FeO₄₀. The magnetic behavior was examined by means of vibrating sample magnetometry. The results showed a change in the magnetic order from antiferromagnetic for the undoped sample to the ferromagnetic order for the co-doped samples. This change is attributed to the modulations in the magnetic moment due to crystal structure distortions. All samples show high relative permittivity values, which were enhanced by doping with Sr²⁺. Ni²⁺ cations increase the dielectric dissipation factor; this enhancement is related to their interactions with cations of a different oxidation state, such as Fe³⁺, Fe²⁺, Ni²⁺, Bi³⁺ and Sr²⁺ in the crystal structure of BiFeO₃. The magnetoelectric coupling that was evaluated using magnetodielectric measurements was above 4% at 1?kHz for the higher applied magnetic field of 18?kOe.