Reduction of Escherichia coli O157:H7 population on baby spinach leaves by liquid sanitizers

The effectiveness of various liquid sanitizers and methods of application against Escherichia coli on baby spinach was investigated. Inoculated spinach was treated with (i) Pro‐San L (commercially prepared solution containing 0.66% citric acid, 0.036% sodium dodecyl sulfate (SDS); (ii) chlorine solution (200 ppm), alone or with addition of 0.036% SDS; and (iii) aqueous solution of 0.66% levulinic acid with 0.036% SDS. Population reduction in response to these treatments ranged between 2.1 and 2.8 log CFU/g. No significant difference (p > .05) was found among tested sanitizers in microbial count reduction. Spraying, dipping, and “dry” vacuum impregnation methods of Pro‐San L application were compared. Dipping was the most effective in reducing E. coli O157:H7 population (4.4 log CFU/g reduction). Dry vacuum impregnation was less effective (3.3 log CFU/g reduction) and caused damage to the produce. The effectiveness of spray Pro‐San L application and holding for prolonged time (up to 3 days) was also evaluated. However, increasing time of exposure to organic acid sanitizer did not increase sanitizing effectiveness and led to progressive damage of spinach leaves.     

Medicated Scaffolds Prepared with Hydroxyapatite/Streptomycin Nanoparticles Encapsulated into Polylactide Microfibers

The preparation, characterization, and controlled release of hydroxyapatite (HAp) nanoparticles loaded with streptomycin (STR) was studied. These nanoparticles are highly appropriate for the treatment of bacterial infections and are also promising for the treatment of cancer cells. The analyses involved scanning electron microscopy, dynamic light scattering (DLS) and Z-potential measurements, as well as infrared spectroscopy and X-ray diffraction. Both amorphous (ACP) and crystalline (cHAp) hydroxyapatite nanoparticles were considered since they differ in their release behavior (faster and slower for amorphous and crystalline particles, respectively). The encapsulated nanoparticles were finally incorporated into biodegradable and biocompatible polylactide (PLA) scaffolds. The STR load was carried out following different pathways during the synthesis/precipitation of the nanoparticles (i.e., nucleation steps) and also by simple adsorption once the nanoparticles were formed. The loaded nanoparticles were biocompatible according to the study of the cytotoxicity of extracts using different cell lines. FTIR microspectroscopy was also employed to evaluate the cytotoxic effect on cancer cell lines of nanoparticles internalized by endocytosis. The results were promising when amorphous nanoparticles were employed. The nanoparticles loaded with STR increased their size and changed their superficial negative charge to positive. The nanoparticles’ crystallinity decreased, with the consequence that their crystal sizes reduced, when STR was incorporated into their structure. STR maintained its antibacterial activity, although it was reduced during the adsorption into the nanoparticles formed. The STR release was faster from the amorphous ACP nanoparticles and slower from the crystalline cHAp nanoparticles. However, in both cases, the STR release was slower when incorporated in calcium and phosphate during the synthesis. The biocompatibility of these nanoparticles was assayed by two approximations. When extracts from the nanoparticles were evaluated in cultures of cell lines, no cytotoxic damage was observed at concentrations of less than 10 mg/mL. This demonstrated their biocompatibility. Another experiment using FTIR microspectroscopy evaluated the cytotoxic effect of nanoparticles internalized by endocytosis in cancer cells. The results demonstrated slight damage to the biomacromolecules when the cells were treated with ACP nanoparticles. Both ACP and cHAp nanoparticles were efficiently encapsulated in PLA electrospun matrices, providing functionality and bioactive properties.     

Inverse emulsion polymerization of triple monomers of acrylamide,maleic anhydride,and styrene to achieve highly hydrophilic–hydrophobic modified polyacrylamide

The purpose of this study was the production of copolymers and terpolymers with highly hydrophilic–hydrophobic properties, using inexpensive and available monomers as potential enhancing oil recovery (EOR) and water production control agents for high-temperature and high-salinity (HTHS) oil reservoirs. For this purpose, several copolymers and terpolymers with different molar percentage of acrylamide/styrene, acrylamide/maleic anhydride, and acrylamide/styrene/maleic anhydride were synthesized by the inverse emulsion polymerization technique. The presence of hydrophobic styrene and hydrophilic maleic anhydride monomers in the copolymer and terpolymer structure, provided some unique properties compared to polyacrylamide, was confirmed by several analyses including HNMR, elemental analysis, FTIR, SEM, TGA, and DSC. Simulating HTHS oil reservoir condition under high salinity, temperature, and shear rate, the rheological studies suggested unlike traditional EOR agents such as polyacrylamide, the viscosity of the copolymer, and terpolymer aqueous solutions showed a considerable increase after a critical polymer concentration and less reduction with the salt increment at both ambient and elevated temperatures. Furthermore, the swelling ratio of the insoluble terpolymers measured versus the time and temperature in salt water increased with the maleic anhydride mole fraction, decreased with the salt concentration, and showed a maximum value at around 57 °C. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47753.     

Microstructural evolution of a commercial ultrafine alumina powder densified by different methods

The densification and grain growth of bodies made from a commercial ultrafine alumina powder was investigated. The primary powder was initially subjected to dry (uniaxial cold pressing) and wet shaping (slip casting), followed by conventional (CS)-, two step (TSS)-, and microwave (MS) sintering to explore the effect of each series of treatments on the densification and microstructural evolution of the specimens. It was demonstrated that a uniform microstructure with higher density would be obtained using the wet shaping method. In addition, microwave sintering was found to be more effective into the densification of the specimens and in yielding a finer grain structure. It is believed that the high heating rate and effective particle packing are responsible for the improvements in these properties. On this basis, it was also demonstrated that the fracture toughness of the samples increased significantly through the application of microwave sintering.     

Multi-band Broad Emission Properties of Fluoren-9-one Oxime Chemically and Physically Confined in a Photoactive Polyphenylsilsesquioxane Network Matrix

The fluoren-9-one oxime luminophore (FO) was covalently incorporated into a photoactive polyphenylsilsesquioxane matrix (PSQ) by an in situ two-step process using different molar ratios of FO and C₆H₅SiCl₃ in an aprotic solvent in the presence of triethylamine base. The infrared (FT-IR), electronic (UV–Vis) and photoluminescence (PL) studies of these materials are reported. Their infrared spectra at room temperature and softening properties suggest that the PSQ matrix adopts a ladder structure rather than a polyhedral cubic cage. The phenyl-based PSQ matrix (C₆H₅PSQ) fluoresces in the violet region at ~325 nm when photo-excited at 270 but relatively photo-passive if excited at 320 nm. However, the untethered free FO luminophore exhibits multi-band PL properties with two intense overlapping emission bands in the blue–green region at 450 and 474 nm, and a moderately intense violet band at 340 nm which suggests the existence of multiple excited states. However, the FO–C₆H₅PSQ composite systems emit violet and blue-greenish light centered, respectively, at ~330 and ~470 nm when photo-excited at 270 nm. On the other hand the violet band was found to disappear when the composites are excited at 320 nm. The blue-greenish band remains irrespective of the mode of FO incorporation into the PSQ matrix being covalently attached or physically doped. PL studies on these materials show that emission by the PSQ matrix has an observable effect on broad band emission of the FO luminophore centers.     

Nodular structure of isotactic polypropylene crystallizes from the melt

This article highlights the melt crystallization behavior of different grades of isotactic polypropylene (iPP) using a hot‐stage polarizing optical microscopy. iPP samples were heated up at a heating rate of 10°C/min passing the melting temperature and then kept for 3 min at a temperature range of 175–200°C before they cooled rapidly at 40°C/min to crystallize isothermally at a range of 130–145°C. It has been found that the temperature at which the samples were kept has a strong effect on the crystallization mode; for samples heated up and kept at temperatures below 190°C, the crystallization started with thin and long rods or nodules, which grew in the circumferential direction only while their lengths remain unchanged as the time passed. The shape of the nodules can be straight, circular, branched, or entangled, and they can grow parallel to each other or they can be crossed or in a random way. This phenomenon disappeared completely for samples melted and kept at temperatures above 195°C. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Investigation on the correlation between rheology and morphology of PA6/ABS blends using ethylene acrylate terpolymer as compatibilizer

Phase morphology and rheological behavior of polyamide 6 (PA6)/acrylonitrile butadiene styrene (ABS) polymers blends was studied using scanning electron microscopy and rheometry. The results showed that the phase morphology and rheological properties depends on blend composition. We evaluated the effect of addition of ABS as dispersed phase and EnBACO‐MAH (ethylene n‐butyl acrylate carbon monoxide maleic anhydride) as a compatibilizer on the morphological and rheological behaviors of PA6/ABS blends. It was concluded that there is a good agreement between the results obtained from rheological and morphological studies. As a consequence, addition of the ABS and compatibilizer weight percent led to a significant change in morphological structure and a great mounting in the viscosity as well as the elasticity. The rheological properties results demonstrate that adding compatibilizer to polymer blends led to increasing the crossover point, which shows a transition from a high viscous to a considerably more elastic behavior. Also, the slow transition of relaxation time peak from the peak of the PA6 to the peak of the ABS implies increasing the miscibility of the PA6/ABS blend components by increasing compatibilizer content. In addition, the Carreau–Yasuda model was used to extract information on rheological properties (zero shear viscosity and relaxation time) for PA6/ABS/EnBACO‐MAH blends by fitting the experimental data with this model. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Supertough (Polyamide 6)/(acrylonitrile butadiene rubber) nano alloy through in situ polymerization of caprolactam in the presence of acrylonitrile butadiene rubber nanophase

In this work, polymerization of caprolactam (CL) was carried out in the presence of acrylonitrile butadiene rubber (NBR) during the reactive melt‐mixing process. During shear mixing, NBR particles swelled and dissolved in the molten CL, which led to separation and distribution of rubber particles to nanoscale in the dissolution stage. Then, in an internal mixer, supertough Polyamide 6 was prepared via melt polymerization of CL/NBR mixture, sodium caprolactam as a catalyst, and hexamethylene diisocyanate as an activator. The effects of various concentrations of catalyst and activator on the initiation time of the reaction were determined. Physical and mechanical properties of different formulations prepared via reactive melt blending were determined by tensile and impact measurements, differential scanning calorimetry, Fourier‐transform infrared spectroscopy, X‐ray scattering techniques, transmission electron microscopy, and dynamic mechanical thermal analysis. Experimental results showed that a recipe with 3% nitrile rubber in a CL/NBR mixture enhances the physical and mechanical properties the best, compared with other formulations. This condition led to the formation of NBR nanospheres during melt polymerization of Polyamide 6 as well. J. VINYL ADDIT. TECHNOL., 21:116–121, 2015. © 2014 Society of Plastics Engineers     

Inactivation of pathogenic Klebsiella pneumoniae by CuO/TiO2 nanofibers: A multifunctional nanomaterial via one-step electrospinning

The fabrication and characterization of one-dimensional CuO/TiO₂ nanofibers with high photocatalytic and antibacterial activities are presented. The CuO/TiO₂ nanofibers were prepared by electrospinning of colloid composed of titanium isopropoxide, poly(vinylpyrroliodine) (PVP) and copper nanoparticles and calcination at 700 °C in air for 1 h. The antibacterial activity was tested using Klebsiella pneumoniae as model organism by calculation of the minimum inhibitory concentration (MIC). The obtained CuO/TiO₂ nanofibers showed prominent photocatalytic activity under visible light to degrade reactive black5 and reactive orange16 dyes in aqueous solutions and effectively catalyze K. pneumoniae inactivation. The decomposition process of the cell wall and cell membrane was directly observed by TEM analysis after the exposure of the K. pneumoniae to the nanofibers. Interestingly, the introduced photocatalyst can be reused with the same photocatalytic activity. Overall, the combination of CuO and TiO₂ can be synergistic and resulted in CuO/TiO₂ composite nanofibers having superior photocatalytic and antimicrobial potential to impede K. pneumoniae growth which causes bacterium to die ultimately.