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The main goal of this work is to correlate morphological parameters of the binary blend of polyamide 6 (PA6) and a polylactide (PLA) based biodegradable co-polyester blend (BioFlex) (scanning electron microscopy, solvent extraction method) with the solid-state mechanical properties (stress strain analysis) as well as thermal (differential scanning calorimetry) and selected physico-chemical characteristics (Fourier transform infrared spectroscopy and water uptake analysis). The blends of PA6/BioFlex were prepared in ratios of 100/0, 90/10, 75/25, 60/40, 50/50, 40/60, 25/75, 10/90 and 0/100 in wt.%. The occurrence of co-continuous morphology was observed within the range of 40 to 60 wt.% of BioFlex. Furthermore, the results show that the co-continuous morphology of PA6/BioFlex blends significantly affected both tensile (E modulus) and thermal properties (melting enthalpy) of the blends. In the case of the tensile properties, the effect of the morphological arrangement was strongly dependent on the deformation range. The presence of BioFlex in the blends reduced the crystallizability of PA6 noticeably. Co-continuous structure formation was observed to have a significant effect on the melting enthalpy of the blend. Composition morphology dependent responses were observed in the case of the FTIR and water uptake studies. [ABSTRACT FROM PUBLISHER]

This work is dedicated to compatibilization process investigation between polyamide 6 and biodegradable polylactide. The process was conducted by newly developed polyalkenyl-poly-maleic-anhydride-imide/amide agents over a selected range of composition to identify morphologies and properties of these blends. The properties of resulted blends were studied by scanning electron microscopy, solvent extraction techniques, mechanical testing, Fourier transform infrared spectroscopy, and differential scanning calorimetry measurements. Results show that blending of the two polymers without compatibilizers produced multiphase blends. It was shown by scanning electron microscopy imaging that addition of prepared compatibilizers reduced a domain size of a dispersed phase and also changes in nearly co-continuous state occurred. Static and dynamic mechanical properties were improved, and especially impact strength and tensile strength were the most sensitive on the presence of compatibilizers. [ABSTRACT FROM PUBLISHER]

Fully and partially hydrolyzed poly(vinyl alcohol) (PVA) was modified with zinc sulphate in the concentration range from 0 to 9 wt% of recalculated zinc content using the solvent cast technique. The resulting polymeric films were characterized by optical microscopy, stress–strain analysis, differential scanning calorimetry and Fourier transform infrared spectroscopy (FT-IR–ATR). In addition, agar diffusion test and dilution and spread plate technique were used for determination of antibacterial properties of the films against both Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli, Pseudomonas aeruginosa and Klebsiella pneumoniae) bacterial strains. A mathematical model was applied on the measured data and parameters characterizing the antibacterial efficiency of the material were calculated and discussed. The results revealed that the PVA hydrolysis degree can play an important role in all studied properties, including antibacterial activity of the all PVA-based materials. [ABSTRACT FROM AUTHOR]

Abstract: There has been a growing interest in developing antibacterial polymeric materials. The logical consequence following development of a new material is optimisation of its processing conditions and investigation of the influence of processing parameters on functionality of a given material. The present work deals with investigation of the effect of preparation temperature on the mechanical and antibacterial properties of polymer films based on poly(vinyl alcohol) (PVA) and silver nitrate (0, 1, 3, 5, 7, 9 wt.% silver content). The mechanical properties of the films prepared at various temperatures (25, 35, 50, 60, 75 °C) were characterized by using stress–strain analysis. Antibacterial properties were determined by using an agar diffusion test and a dilution and spread plate technique against both Gram positive (Staphylococcus aureus) and Gram negative (Escherichia coli, Pseudomonas aeruginosa and Klebsiella pneumoniae). The results show significant effect of the elevated temperature on the samples properties. [Copyright &y& Elsevier]

Poly(vinyl alcohol) (PVA) was modified by zinc nitrate in the concentration range from 0 to 22.29 wt.% using the solvent cast technique. The resulting material was characterized by optical microscopy, stress-strain analysis, differential scanning calorimetry, UV-visible spectroscopy, and Fourier transform-infrared spectroscopy. In addition, the antibacterial properties of the prepared films were tested against the both gram positive and gram negative bacterial strains. The results show the uniform distribution of the modifier within the PVA matrix, enhanced mechanical properties (up to 8.24 wt.%), and good antibacterial activity against gram negative bacteria at low modifier content. [ABSTRACT FROM AUTHOR]

Abstract: Lactose (L) filled (0–40wt.%) composites of metallocene linear low-density polyethylene (mLLDPE) were prepared to get a new, environmentally friendly polymeric material. The effect of L on the material was characterized through its mechanical, physico-chemical and rheological properties, and biodegradability in the composting environment (up to 4 months). The microorganisms present in the compost bed have shown great influence on the properties of the new material, as proved by the weight loss data, changes in FTIR-ATR spectra, tensile and rheological properties. The presence of L in the system does not influence tensile properties significantly up to the content of 40wt.%. The biodegradation of the highest-filled composite has been found substantially higher than that of the others. This is in agreement with the results obtained through surface morphology study by SEM and assessing the presence of microbes in the compost bed where the composites were placed for biodegradation. [Copyright &y& Elsevier]

Blends of poly(lactic acid) (PLA) with poly(propylene carbonate) (PPC) are currently in the phase of intensive study due to their promising properties and environmentally friendly features. Intensive study and further commercialization of PPC-based polymers or their blends, as usual, will soon face the problem of their waste occurring in the environment, including soil. For this reason, it is worth comprehensively studying the degradation rate of these polymers over a long period of time in soil and, for comparison, in phosphate buffer to understand the difference in this process and evaluate the potential application of such materials toward agrochemical and agricultural purposes. The degradation rate of the samples was generally accompanied by weight loss and a decrease in molecular weight, which was facilitated by the presence of PPC. The incubation of the samples in the aqueous media yielded greater surface erosions compared to the degradation in soil, which was attributed to the leaching of the low molecular degradation species out of the foils. The phytotoxicity study confirmed the no toxic impact of the PPC on tested plants, indicating it as a "green" material, which is crucial information for further, more comprehensive study of this polymer toward any type of sustainable application. [ABSTRACT FROM AUTHOR]

The aim of this study was to develop a novel amikacin (AMI) delivery system with prolonged release based on composite electrospun nanofibers of PLA supplemented with AMI-loaded Si nanoparticles of different morphology. The resultant materials were characterized in terms of their physical properties (scanning electron microscopy, Brunauer–Emmett–Teller analysis, thermogravimetric analysis, water contact angle). High-Performance Liquid Chromatography was used to determine the AMI content in the liquid fractions obtained from the release study. The results show that nanofibers of fumed silica exhibited an aggregated, highly porous structure, whereas nanofibers of mesoporous silica had a spherical morphology. Both silica nanoparticles had a significant effect on the hydrophilic properties of PLA nanofiber surfaces. The liquid fractions were investigated to gauge the encapsulation efficiency (EE) and loading efficiency (LE) of AMI, demonstrating 66% EE and 52% LE for nanofibers of fumed silica compared to nanofibers of mesoporous silica nanoparticles (52% EE and 12.7% LE). The antibacterial activity of the AMI-loaded nanofibers was determined by the Kirby–Bauer Method. These results demonstrated that the PLA-based silica nanofibers effectively enhanced the antibacterial properties against the Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae. [ABSTRACT FROM AUTHOR]

This study is focussed on micro-encapsulation of essential oils in polylactic acid (PLA) and a poly(methyl methacrylate) (PMMA) matrix as well as blends of the same. Microspheres were prepared by the solvent evaporation technique and characterised by scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and Fourier transform infra-red spectroscopy (FTIR). The encapsulation efficiencies and release profiles of the essential oils were studied by gas chromatography mass spectrometry (GC-MS) and head-space solid-phase microextraction GC-MS, respectively. Furthermore, the microspheres were tested for antibacterial activity against both Gram-negative and Gram-positive bacterial strains. The results showed that the microspheres compositions (PLA/PMMA ratio) have significant effect on their characteristics. The process adopted for preparing the microspheres promoted formation of spherical particles at the sizes of 1.5–9.5 µm. The highest encapsulation efficiency of the prepared microspheres was observed in systems consisting of linalool (81.10 ± 10.0 wt. % for PLA system and 76.0 ± 3.3 wt. % for PMMA system). Confirmation was also made that the release rate of the microspheres was affected by the size of the same. [ABSTRACT FROM AUTHOR]

This manuscript details the preparation and characterization of a renewable biocomposite material intended as a soil conditioner based on low-molecular-weight poly(lactic acid) (PLA) and residual biomass (wheat straw and wood sawdust). The swelling properties and biodegradability of the PLA-lignocellulose composite under environmental conditions were evaluated as indicators of its potential for applications in soil. Its mechanical and structural properties were characterized by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Results showed that the incorporation of lignocellulose waste material into PLA increased the swelling ratio of the biocomposite by up to 300%. The application of the biocomposite of 2 wt% in soil enhanced its capacity for water retention by 10%. In addition, the cross-linked structure of the material proved to be capable of swelling and deswelling repeatedly, indicating its good reusability. Incorporating lignocellulose waste in the PLA enhanced its stability in the soil environment. After 50 days of the experiment, almost 50% of the sample had degraded in the soil. [ABSTRACT FROM AUTHOR]

A set of renewable and biodegradable hydrogels based on acid whey and cellulose derivatives blended with poly(lactic acid) (PLA) were designed as eco-friendly biopolymeric material for sustainable agricultural applications. The physico-chemical properties of the hydrogel were evaluated using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and rheological measurements. The effect of the whey/polysaccharide/PLA hydrogel on soil quality improvement (water retention study, biodegradability, loading capacity and release of the fertilizers) and the growth pattern of Raphanus sativus and Phaseolus vulgaris has been also studied. The addition of PLA has been found to improve mechanical properties of the hydrogel. The introduction of 20% wt PLA extended decomposition time of hydrogels by 25% which makes the material more stable in the environment and maintaining the soil humidity for longer. The increasing the amount of PLA led to a rise in hydrogel viscosity brought about better entrapment efficiency of the fertilizers (86–92% for KNO 3 and 87–96% for urea, resp.) compared to control (82% for KNO 3 and 85% for urea, resp.). The novel hydrogels with swelling ratio of up to 500% showed potential as a sustainable water reservoir for plants improving water retention capacity of the soil by 30%. • Renewable and biodegradable whey/cellulose derivatives-based hydrogels mixed with low-molecular weight PLA were prepared. • Effect of different PLA content on hydrogel properties was evaluated • The hydrogels demonstrate a high water holding capacity and excellent biodegradability. • Acting as a source of water a nutritive whey agents for plants and for slow release of fertilizers. • Promising alternative to commercial hydrogels based on synthetic polymers. [ABSTRACT FROM AUTHOR]

Exposure to endocrine-disrupting chemicals (EDCs) has been linked to harmful effects in biota due to their widespread chemical persistence. In this paper, we report on the fabrication of electrospun polylactic acid (PLA) based nanofibers functionalized with TiO 2 nanoparticles. The PLA-based TiO 2 nanofibers were further stabilized with the incorporation of halloysite (HNT) particles. The nanofibers were fabricated in varied concentrations of HNT (5, 10, 15%), while TiO 2 was kept at 10% for all the prepared samples. The fabricated samples were evaluated for elimination of synthetic 17α-ethinylestradiol (EE2) hormone as a model EDC pollutant. By using combined adsorptive and photocatalytic processes, the as-prepared samples were evaluated in a continuous flow system under dark and UV-light irradiation for EE2 removal. The best-performing sample with an optimized concentration of PLA/TiO 2 /HNT (85, 10, 5%) was able to eliminate 71.6% of EE2 hormone under UV irradiation at a hormone concentration of 0.1 mg/L. The maximum removal capacity obtained was 1.26 mg/g in 2 h, which best fitted the pseudo-first-order kinetics model. The sample was further utilized for additional experiments by changing experimental parameters, such as contact time, solution pH, and flow rate. To elucidate the actual degradation of the EE2 hormone, LCMS analysis was carried out to monitor the formation of by-products, which indicated that EE2 was fragmented into different potentially benign molecules. Finally, the best-performing sample was utilized for ten cyclic runs under optimized conditions for which the sample maintained sufficiently high degradation without any loss in structural integrity. Overall, the results showed that the developed PLA/TiO 2 /HNT nanofibers have a high potential to target persistent organic pollutants. [Display omitted] • PLA-based nanofibers were functionalized with TiO 2 and HNT nanoparticles. • The as-prepared nanofibers were evaluated using ethinylestradiol hormone. • Elimination of EE2 by tandem synergistic adsorptive and photocatalysis processes. • Reusability of the fibers was determined after ten cyclic operations. • LCMS analysis was carried out to identify the formation of degraded byproducts. [ABSTRACT FROM AUTHOR]

Nanocellulose (NC), a one-dimensional nanomaterial, is considered a sustainable material for water and wastewater purification because of its promising hydrophilic surface and mechanical characteristics. In this regard, nanostructured membranes comprising NC and two-dimensional (2D) nanomaterials emerged as advanced membranes for efficient and sustainable water purification. This article critically reviews the recent progress on NC-2D nanostructured membranes for water and wastewater treatment. The review highlights the main techniques employed to fabricate NC-2D nanostructured membranes. The physicochemical properties, including hydrophilicity, percent porosity, surface roughness, structure, and mechanical and thermal stability, are summarized. The key performance indicators such as permeability, rejection, long operation stability, antifouling, and interaction mechanisms are thoroughly discussed to evaluate the role of NC and 2D nanomaterials. Finally, summary points and future development work are highlighted to overcome the challenges for potential practical applications. This review contributes to the design and development of advanced membranes to solve growing water pollution concerns in a sustainable manner. [Display omitted] [ABSTRACT FROM AUTHOR]

This work describes the preparation of a novel biopolymer hydrogel based on acid whey, cellulose derivatives and polyvinyl alcohol (PVA). The hydrogel was prepared and characterized with the aim of producing an environmentally-friendly soil amendment to increase water retention capacity of the soil. The findings showed considerable swelling properties of the hydrogels depending on the PVA content and crosslinking density. The samples with PVA in a concentration 2.5 % and 5 % were more rigid, the gel fraction increased with a subsequently decrease in their swelling capacity. The hydrogels crosslinked with 15 % of citric acid demonstrated a constant swelling ratio (SR) of around 500 % within 10 swelling/drying cycles. The hydrogels crosslinked with 10 % citric acid and supplemented with 1 % of PVA showed SR of 1000–1400 % caused by less crosslinked polymer network and increased pore volume for water uptake. It was found that hydrogel with a higher gel fraction had a stable structure. Supplementing PVA at 5 % extended the period of decomposition of the hydrogel material by almost 60 % in the soil environment and soil humidity was maintained for longer. Applying 2 % of the hydrogel 5PVA to soil increased the water retention capacity by 19 %. • An environmentally-friendly soil conditioner was prepared for sustainable agricultural applications. • The effect of polyvinyl alcohol on the swelling properties and biodegradability of the hydrogels was evaluated. • Addition of 5 % PVA extended the period of biodegradation of the hydrogel in soil by almost 60 %. • The results show the potential of acid whey to be a source of nutritive whey agents for plants. [ABSTRACT FROM AUTHOR]

There are several methods for synthesizing polylactic acid. Solid-state polymerization is one of the most promising methods due to the great feasibility and beneficial properties of the final polymer. In terms of this study, the purpose was to evaluate the effect of various catalyst systems (based on tin dichloride, tin dioxide, tin octoate, citric acid, sulphuric acid, toluenesulfonic acid and methane sulfonic acid) and focus on the molecular weight, structure and thermal properties of the final products. The molecular weight was shown to be controlled by different catalytic systems and Mw > 100,000 g/mol was achieved after 24 h of synthesis, which is more than in the conventional melt polycondensation process. Thermal stability was found to be negatively affected by the catalytic system, although relatively positive results can still be achieved. [ABSTRACT FROM PUBLISHER]

Poly(3-hydroxybutyrate) is a biopolymer which is used to production of implants in the human body. On the other hand, the physical and mechanical properties of poly(3-hydroxybutyrate) are compared to the properties of isotactic polypropylene what makes poly(3-hydroxybutyrate) possible substitute for polypropylene. Unfortunately, the melting point of poly(3-hydroxybutyrate) is almost equal to its degradation temperature what gives very narrow window of its processing conditions. Therefore, numerous attempts are being made to improve the poly(3-hydroxybutyrate) properties. In the present work, hybrid nanobiocomposites based on poly(3-hydroxybutyrate) as a matrix with the use of organic nanoclay - Cloisite 30B and linear polyurethane as a second filler have been manufactured. The linear polyurethane was based on diphenylmethane 4,4'-diisocyanate and diol with imidazoquinazoline rings. The obtained nanobiocomposites were characterized by X-ray diffraction, scanning and transmission electron microscopies, thermogravimetry, differential scanning calorimetry and their selected mechanical properties were tested. The resulting hybrid nanobiocomposites have intercalated/exfoliated structure. The nanobiocomposites characterize a higher thermal stability and a wider range of processing temperatures compared to the unfilled matrix. The plasticizing influence of nanofillers was also observed. In addition, the mechanical properties of the discussed nanobiocomposites were examined and compared with those ones of the unfilled poly(3-hydroxybutyrate). The new-obtained nanobiocomposites based on poly(3-hydroxybutyrate) containing 1% Cloisite 30B and 5% by mass of the linear of polyurethane characterized the highest improvement of processing conditions. They have the biggest difference between the temperature of degradation and the onset melting temperature, about 100°C. [ABSTRACT FROM AUTHOR]

In this work, research concerning the synthesis and properties of linear polyurethanes (PUs) with the imidazoquinazoline rings was represented. Reaction conditions of 2,6-bis(2-hydroxyethyl)-1-phenylimida-zo[1,5-c]quinazoline-3,5-dione (BHPIQ) with 1,6-hexamethylene diisocyanate were determined and optimized. These conditions are adapted to reaction of BHPIQ with 4,4′-diphenylmethane diisocyanate and 2,4-toluene diisocyanate. New PUs with imidazoquinazoline rings were characterized by spectral methods (1H-NMR and IR spectroscopies), which confirm their structures. Their molar masses and dispersity index were measured by size exclusion chromatography method. The wide-angle X-ray scattering and differential scanning calorimetry (DSC) studies have shown that all PUs based on BHPIQ are amorphous. Moreover, thermal properties of PUs were investigated by thermogravimetry analysis, standard DSC, and temperature-modulated DSC methods. During thermogravimetric measurements, the exhaust gases were analyzed by FTIR method. Incorporation of imidazoquinazoline ring into the PU chains escalates their glass transition temperature; thus, their heat resistance was enhanced. Furthermore, their degradation rate and the amount of released degradation products were reduced. The investigated properties of the obtained PUs with imidazoquinazoline rings were compared with those ones of suitable PUs based on 1,4-butanediol. Linear polyurethanes were obtained in reaction of 1-phenyl-2,6-bis(2-hydroxyethylimidazo[1,5-c]quinazoline-3,5-dione with hexamethylene 1,6-diisocyanate, 4,4′-diphenylmethane diisocyanate and toluene 2,4-diisocyanate. Their composition and structure were confirmed. The phase contents and thermal properties were investigated [ABSTRACT FROM AUTHOR]

The present research was undertaken to develop a chitosan-collagen film for controlled delivery of combinations of local anesthetics. The film has been prepared by casting which is a versatile, rapid and low-cost approach distinguished by high reproducibility. The mechanical, morphological, and physicochemical properties of the films and the impact of the drug loading were evaluated. We showed that the formulations have a good combination of strength and flexibility with high water permeability. Surface morphology investigation indicates a variation in roughness depending on the loaded compound. Release studies were performed in controlled environments and the data processed by the Higuchi model to assess the dynamics of the release. The local anesthetics, lidocaine, tetracaine, and benzocaine, were uniformly distributed within the matrix and released in a rate and magnitude specific for the drug concentration and combination tunable in a range time from 6 h to 24 h. The films dissolve completely in the physiological environment within 24 h without leaving any toxic metabolites as both of the components are recognized as safe. In vitro cytotoxicity and cell proliferation tests performed on human dermal fibroblast demonstrate the biocompatibility and lack of cytotoxicity of the prepared formulations. [ABSTRACT FROM AUTHOR]

Nowadays, the magnetorheological elastomers (MREs) represent an important composite group with a wide range of applications. They are however predominantly typified by chemically cross-linked polymer matrices which makes them difficult to be reprocessed or recycled. Here, we demonstrate the concept of the MREs' reprocessing for the first time. The thermoplastic elastomer (TPE) was adopted as a suitable matrix allowing the MRE production via injection-molding, while making them also reusable. Each processing iteration was accompanied by thermo-mechanical degradation causing the gradual TPE oxidation, decrease in the TPE molecular weight and a viscosity reduction of their melts. In the MREs, the unexpected processing-induced particle/matrix bonding was revealed, which promoted their stiffening. As a result, the magnetic field-induced particle mobility was limited decreasing the magnetorheological activity of the MREs by tens of percent per the processing cycle. We expect that the injection-molded TPE-based MREs could offer a new pathway for producing the smart engineering composites owing to the ability to be easily reprocessed. [ABSTRACT FROM AUTHOR]

The work is focused on the development of microspheres based on the combination of two polysaccharides; chitosan and alginic acid with the aim to allocate, hold, release and protect environmentally sensible molecules. The microspheres were prepared using a solvent-free, low cost and scalable approach and two enzymes; trypsin and protease from Aspergillus Oryzae have been used as a model to evaluate the microspheres peculiarities. The proteins were encapsulated during the microspheres preparation. The relationship between the polysaccharides weight ratio and the morphology, stability and ability of the carrier to allocate the enzymes has been evaluated. The enzymatic activity and the release kinetics were assessed in different conditions to assess the impact of the external environment. Obtained results demonstrate the efficacy of the prepared microspheres to preserve the activity of relevant bioactive compounds which are highly relevant in food, cosmetic and pharmaceutic, but the application is limited due to their high sensibility. [ABSTRACT FROM AUTHOR]

Abstract This work investigates the thermal stability of bacteriocin nisin in polylactide (PLA) and polylactide/polyethylene glycol (PLA/PEG) blends at temperatures of 90 °C–180 °C. The samples were prepared by solvent cast technique and characterized according to their mechanical and thermal properties. Research on the thermal stability of nisin in the PLA and PLA/PEG systems was carried out by exposing the given films to various temperatures (90 °C, 120 °C, 160 °C, and 180 °C) for a duration of up to 48 h. Assessment of the antibacterial activity of the samples was carried out by the agar diffusion method against Micrococcus luteus , while structural analysis involved the use of high-performance liquid chromatography with mass detection. Structural changes in the polymer matrix were evaluated by gel permeation chromatography and scanning electron microscopy. The results showed that nisin retained almost 70% of its antimicrobial activity in the PLA matrix, even after treatment at 160 °C for 15 min. The presence of PEG significantly enhanced the degradation of nisin above 120 °C. Highlights • The issue related to natural based bacteriocin, nisin, as antibacterial modifier of polymers is discussed. • Nisin stability and antibacterial activity in PLA was investigated at temperatures simulating the thermoplastic processing. • Nisin incorporated in PLA matrix sustain its antibacterial activity even after exposure to temperatures corresponding to PLA melting point. [ABSTRACT FROM AUTHOR]

β-carotene is a natural compound with significant antioxidant activity. However, its poor solubility in water and low stability reduce its potential application. Innovative polyplexes based on the combination of amphiphilic chitosan assembled with DNA have been developed using a solvent-free, simple and low-cost method with the aim to load, retain and enhance the antioxidant capability of β-carotene. The polyplexes, with dimension about 100 nm, and excellent stability, were able to hold up to 400 μg of β-carotene per mg of the carrier, with minimal loss till two weeks. The antioxidant activity was significantly enhanced after loading, as demonstrated using two well known methods. Cytotoxicity assay confirmed the not toxicity of the system. The results suggest the polyplexes as an excellent candidate to develop formulation able to preserve and enhance the peculiarities of compounds which are used mainly in food, cosmetic and pharmaceutic but with still some limitations. [ABSTRACT FROM AUTHOR]

This work investigates the degradation and properties of a thermoplastically prepared composite comprising a polylactide/hybrid zinc stearate-silver system. The influence of the zinc stearate-silver system on the properties of the composite is investigated by electron microscopy, differential scanning calorimetry and tensile tests. Furthermore, the antimicrobial activities of the systems are examined. The degradation behaviour of the composites is studied in both abiotic and biotic (composting) environments at an elevated temperature of 58 °C. The results reveal good dispersion of the additive in the PLA matrix, a stabilizing effect exerted by the same on the polylactide matrix during processing, and slight reduction in glass transition temperature. The zinc stearate-silver component also reduces brittleness and extends elongation of the composite. Abiotic hydrolysis is not significantly affected, which is in contrast with pure PLA, although mineralization during the early stage of biodegradation increases noticeably. The composite exhibits antimicrobial activity, even at the lowest dosage of the zinc stearate/silver component (1 wt%). Moreover, Ag and Zn contents were found to be present in the composite during abiotic hydrolysis, which was demonstrated by minimal diffusion of Ag ions from the matrix and very extensive washing of compounds that contained Zn. [ABSTRACT FROM AUTHOR]

Composite materials based on PLA have been studied in depth for many applications, including food packaging. This manuscript describes extensive research conducted on a biodegradable polymer (PLA), inorganic filler (CaCO 3), and polyester-based plasticizer (PEP, based on a copolymer of low-molecular-weight PLA and PEG) prepared under semi-industrial conditions, as applicable for the packaging of hot food. The properties of the composite were achieved by post-processing annealing, notably its thermal stability, thereby permitting contact of the material with hot food. The manner of processing was deemed suitable for deployment at an industrial scale, moreover, the thermal stability of the final product endured, evidencing its applicability for such packaging. Change in the morphology of the structure of the composite material depended on the composition and annealing process, as detailed herein. The effect of the post-production thermal annealing on the molecular weight of samples was studied using the gel permeation chromatography. The thermal properties of the composites were investigated by differential scanning calorimetry, dynamic mechanical analysis, and thermogravimetric analysis. The crystallinity was assessed using X-ray diffraction technique, while mechanical behavior was tested in relation to the given tensile properties, shape stability at high temperature, and permeability by the transmission rates of gas/water vapor. [Display omitted] • PLA composite with CaCO 3 and plasticizer was prepared under semi-industrial conditions with a post-processing annealing. • The properties of the composite depended on the morphology and volume fractions of the crystalline and amorphous regions. • The two additive components and given technological conditions lends shape stability to the composite. • The composite was suitable for contact with hot food or use as packaging for foodstuffs that are heated in microwave ovens. [ABSTRACT FROM AUTHOR]

An innovative microcarrier based on a carboxy-enriched and branched polylactic acid derivative was developed to enhance the in vitro phototoxicity of the photosensitizer and prodrug 5-aminolevulinic. Microparticles, prepared by double emulsion technique and loaded with the prodrug were carefully characterized and the effect of the polymer structure on the chemical, physical and biological properties of the final product was evaluated. Results showed that microparticles have a spherical shape and ability to allocate up to 30 μg of the photosensitizer per mg of carrier despite their difference in solubility. Release studies performed in various simulated physiological conditions demonstrate the influence of the branched structure and the presence of the additional carboxylic groups on the release rate and the possibility to modulate it. In vitro assays conducted on human epithelial adenocarcinoma cells proved the not cytotoxicity of the carriers in a wide range of concentrations. The hemocompatibility and surface proteins adsorption were evaluated at different microparticles concentrations to evaluate the safety and estimate the possible microparticles residential time in the bloodstream. The advantages, of loading 5-aminolevulinic acid in the prepared carrier has been deeply described in terms of enhanced phototoxicity, compared to the free 5-aminolevulinic acid formulation after irradiation with light at 635 nm. The obtained results demonstrate the advantages of the prepared derivative compared to the linear polylactide for future application in photodynamic therapy based on the photosensitizer 5-aminolevulinic acid. [ABSTRACT FROM AUTHOR]

Polysaccharides based nanocomplexes have been developed for encapsulation, controlled delivery and to enhance the phototoxicity of the photosensitizer 5-aminolevulinic acid for application in photodynamic therapy. The nanocomplexes were prepared by coacervation in a solvent free environment using chitosan as polycation while alginic and polygalacturonic acid as polyanions. The complexes showed average dimension in the range 90–120 nm, good stability in simulated physiological media and high drug encapsulation efficiency, up to 800 μg per mg of carrier. Release studies demonstrate the possibility to tune the overall release rate and the intensity of the initial burst by changing the external pH. Cytotoxicity and photocytotoxicity tests confirmed the not toxicity of the used polysaccharides. Cell viability results confirmed the improvement of 5-aminolevulinic acid phototoxicity when loaded into the carrier compared to the free form. No effect of the irradiation on the nanocomplexes structure and on the release kinetics of the drug was observed. The results demonstrate that the prepared formulations have suitable properties for future application in photodynamic therapy and to ameliorate the therapeutic efficacy and overcome the side-effects related to the use of the photosensitizer 5-aminolevulinic acid. [ABSTRACT FROM AUTHOR]

In this work, nanocomplexes based on chitosan grafted by carboxy-modified polylactic acid (SPLA) were prepared with the aim of loading simultaneously two anticancer drugs – doxorubicin and 5-fluorouracil, as well as to control their release, reduce the initial burst and boost cytotoxicity. The SPLA was prepared by a polycondensation reaction, using pentetic acid as the core molecule, and linked to the chitosan backbone through a coupling reaction. Nanocomplexes loaded with both drugs were formulated by the polyelectrolyte complexation method. The structure of the SPLA was characterized by 1 H NMR, while the product CS-SPLA was analyzed by FTIR-ATR to prove the occurrence of the reaction. Results showed that the diameters and ζ -potential of the nanocomplexes fall in the range 120–200 nm and 20–37 mV, respectively. SEM and TEM analysis confirmed the spherical shape and dimensions of the nanocomplexes. The presence of hydrophobic side chain SPLA did not influence the encapsulation efficiency of the drugs but strongly reduced the initial burst and prolonged release over time compared to unmodified chitosan. MS analysis showed that no degradation or interactions between the drugs and carrier were exhibited after loading or 24 h of release had taken place, confirming the protective role of the nanocomplexes. In vitro tests demonstrated an increase in the cytotoxicity of the drugs when loaded in the prepared carriers. [ABSTRACT FROM AUTHOR]

The use of organic-inorganic hybrid nanocarriers for controlled release of anticancer drugs has been gained a great interest, in particular, to improve the selectivity and efficacy of the drugs. In this study, iron oxide nanoparticles were prepared then surface modified via diazonium chemistry and coated with chitosan, and its derivative chitosan-grafted polylactic acid. The purpose was to increase the stability of the nanoparticles in physiological solution, heighten drug-loading capacity, prolong the release, reduce the initial burst effect and improve in vitro cytotoxicity of the model drug doxorubicin. The materials were characterized by DLS, ζ-potential, SEM, TGA, magnetization curves and release kinetics studies. Results confirmed the spherical shape, the presence of the coat and the advantages of using chitosan, particularly its amphiphilic derivative, as a coating agent, thereby surpassing the qualities of simple iron oxide nanoparticles. The coated nanoparticles exhibited great stability and high encapsulation efficiency for doxorubicin, at over 500 μg per mg of carrier. Moreover, the intensity of the initial burst was clearly diminished after coating, hence represents an advantage of using the hybrid system over simple iron oxide nanoparticles. Cytotoxicity studies demonstrate the increase in cytotoxicity of doxorubicin when loaded in nanoparticles, indirectly proving the role played by the carrier and its surface properties in cell uptake. [ABSTRACT FROM AUTHOR]

This work is focused on preparation of novel porous type of core–shell-structured microparticles based on polylactide (shell) and poly(vinyl alcohol) cross-linked with glutaric acid (GA) (core) prepared by water-in-oil-in-water solvent evaporation technique. The microparticle systems were used as delivery systems for immobilisation of model antibacterial agent – nisin. The effect of cross-linking and the initial amount of nisin on their morphology was investigated using scanning electron microscopy, BET analysis, zeta potential measurement and Fourier transform infra-red spectroscopy. Encapsulation efficiency and release profile of nisin from the microparticles were studied by high performance liquid chromatography. Antibacterial activity of the prepared systems was tested by dilution and spread plate technique. Results showed the microparticles in the size range of 9–16 μm in diameter with spherical multi-hollow core–shell structure. The presence of cross-linking agent GA influences the release profile of the peptide and has synergistic effect onListeria monocytogenesgrowth reduction. [ABSTRACT FROM AUTHOR]

In the presented work, amphiphilic nanoparticles based on chitosan and carboxy-enriched polylactic acid have been prepared to improve the stability of the pro-drug temozolomide in physiological media by encapsulation. The carrier, with a diameter in the range of 150-180 nm, was able to accommodate up to 800 μg of temozolomide per mg of polymer. The obtained formulation showed good stability in physiological condition and preparation media up to 1 month. Temozolomide loaded inside the carrier exhibited greater stability than the free drug, in particular in simulated physiological solution at pH 7.4 where the hydrolysis in the inactive metabolite was clearly delayed. CS-SPLA nanoparticles demonstrated a pH-dependent TMZ release kinetics with the opportunity to increase or decrease the rate. Mass spectroscopy, UV-Vis analysis, and in vitro cell tests confirmed the improvement in temozolomide stability and effectiveness when loaded into the polymeric carrier, in comparison with the free drug. [ABSTRACT FROM AUTHOR]

This paper focuses on preparing and characterizing nonlinear, highly carboxylic-functionalized poly(lactic acid) copolymer prepared through a reaction between poly(acrylic acid) and lactic acid. The resultant copolymer exhibits a comb architecture, in which poly(acrylic) acid creates the backbone and poly(lactic acid) its side arms. Thorough analysis was conducted on the molecular weight of polymers by gel permeation chromatography through triple detection of light-scattering and viscometry. Each copolymer property was studied in detail. Finally, cytotoxicity assay was also performed. Results showed that comb and multi-comb macromolecular architectures co-existed in the sample and that their size and amount are easily tuneable by ratio of the initial reactant. [ABSTRACT FROM AUTHOR]

Polysaccharide-based nanocomplexes, intended for simultaneous encapsulation and controlled release of 5-Fluorouracil (5-FU) and Temozolomide (TMZ) were developed via the complexation method using chitosan, alginic and polygalacturonic acid. Investigation focused on the influence of polysaccharides on the properties of the system and amelioration of the stability of the drugs, in particular TMZ. The dimensions of particles and their ζ -potential were found to range between 100 and 200 nm and − 25 to + 40 mV, respectively. Encapsulation efficiency varied from 16% to over 70%, depending on the given system. The influence of pH on the release and co-release of TMZ and 5-FU was evaluated under different pH conditions. The stability of the loaded drug, in particular TMZ, after release was evaluated and confirmed by LC–MS analysis. Results suggested that the amount of loaded drug(s) and the release rate is connected with the weight ratio of polysaccharides and the pH of the media. One-way ANOVA analysis on the obtained data revealed no interference between the drugs during the encapsulation and release process, and in particular no hydrolysis of TMZ occurred suggesting that CS-ALG and CS-PGA would represent interesting carriers for multi-drug controlled release and drugs protection. [ABSTRACT FROM AUTHOR]

Polyelectrolytic multilayers (PEMs) with enhanced antibacterial properties were built up onto commercial poly(ethylene terephthalate) (PET) films based on the layer by layer assembling of bacterial contact killing chitosan and bacterial repelling highly hydrated hyaluronic acid. The optimization of the aminolysis modification reaction of PET was carried out by the study of the mechanical properties and the surface characterization of the modified polymers. The layer by layer assembly was successfully monitored by TEM microscopy, surface zeta-potential, contact angle measurements and, after labeling with fluorescein isothiocyanate (FTIC) by absorption spectroscopy and confocal fluorescent microscopy. Beside, the stability of the PEMs was studied at physiological conditions in absence and in the presence of lysozyme and hyaluronidase enzymes. Antibacterial properties of the obtained PEMs against Escherichia coli were compared with original commercial PET. [ABSTRACT FROM AUTHOR]

Chitosan and chitosan-grafted polylactic acid as a matrix for BSA encapsulation in a nanoparticle structure were prepared through a polyelectrolyte complexation method with dextran sulfate. Polylactic acid was synthetized via a polycondensation reaction using the non-metal-based initiator methanesulfonic acid and grafted to the chitosan backbone by a coupling reaction, with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide as the condensing agent. The effect of concentration of the polymer matrix utilized herein on particle diameter, ζ-potential, encapsulation efficiency, and the release kinetic of the model protein bovine serum albumin at differing pH levels was investigated. The influence of pH and ionic strength on the behavior of the nanoparticles prepared was also researched. Results showed that grafting polylactic acid to chitosan chains reduced the initial burst effect in the kinetics of BSA release from the structure of the nanoparticles. Furthermore, a rise in encapsulation efficiency of the bovine serum albumin and diminishment in nanoparticle diameter were observed due to chitosan modification. The results suggest that both polymers actually show appreciable encapsulation efficiency; and release rate of BSA. CS-g-PLA is more suitable than unmodified CS as a carrier for controlled protein delivery. [ABSTRACT FROM AUTHOR]

The authors investigate the efficiency of various catalysts (22 types, based on oxides, carbonates, chlorides, organometallic compounds, N-heterocyclic carbine based compounds, cadmium acetate and molecular sieves) in the process of poly(sebacic acid) anhydride (PSA) synthesis. Their efficiency was studied utilizing methods that characterize the molecular weight distribution (gel permeation chromatography, GPC), structure (Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR), mass spectroscopy (MS)) and thermal properties (differential scanning calorimetry, (DSC), thermogravimetry (TGA)) of the final products. Such structural characterization gave good insight into the resulting polymer structure. Findings reveal the crucial role of catalyst selection in the resulting properties of PSA. The maximum M values reached were found at approximately 280 kg.mol, which in the case of the calcium oxide catalyst was achieved after 60 min of reaction. TGA analyses showed a two-step thermal degradation process for all samples. No significant effect of the catalyst used was observed on polyanhydride thermal stability. However, it was proven that such catalysts do significantly influence the crystallinity of the resulting polyanhydrides. [ABSTRACT FROM AUTHOR]

This study describes the development of a renewable and biodegradable biopolymer-based hydrogel for application in agriculture and horticulture as a soil conditioning agent and for release of a nutrient or fertilizer. The novel product is based on a combination of cellulose derivatives (carboxymethylcellulose and hydroxyethylcellulose) cross-linked with citric acid, as tested at various concentrations, with acid whey as a medium for hydrogel synthesis in order to utilize the almost unusable by-product of the dairy industry. The water uptake of the hydrogel was evaluated by swelling tests under variations in pH, temperature and ion concentration. Its swelling capacity, water retention and biodegradability were investigated in soil to simulate real-world conditions, the latter being monitored by the production of carbon dioxide during the biodegradation process by gas chromatography. Changes in the chemical structure and morphology of the hydrogels during biodegradation were assessed using Fourier transform infrared spectroscopy and scanning electron microscopy. The ability of the hydrogel to hold and release fertilizers was studied with urea and KNO3 as model substances. The results not only demonstrate the potential of the hydrogel to enhance the quality of soil, but also how acid whey can be employed in the development of a soil conditioning agent and nutrient release products. [ABSTRACT FROM AUTHOR]

Medical-grade polyvinyl chloride was modified by incorporation of silver nitrate in a concentration range from 0 to 5 wt.% using a solvent casting technique. Agar diffusion test was performed to evaluate in-vitro antimicrobial properties of prepared samples. The obtained systems were characterized by tensile test, X-ray photoelectron spectroscopy, scanning electron microscopy, and optical microscopy. The micrographs revealed a better morphological disposition of silver particles along the polyvinyl chloride matrix in the samples cast fromN,N-dimethylformamide. Nevertheless, the applied modification did not appreciably influence the tensile properties of the prepared systems compared to the reference samples. [ABSTRACT FROM AUTHOR]

Abstract: This work describes differences between the degradation of poly(l-lactic acid) bulky samples in high partial pressure of a water vapour environment versus a buffered liquid medium. Analytical techniques (optical and electron microscopy, size exclusion chromatography, differential scanning calorimetry) were used to evaluate the material''s morphology, molecular weight, crystallinity and thermal properties. In particular, the extent of degradation was studied separately in the core and surface of the testing specimens. The results reveal significant differences in the bulk degradation profiles and morphological changes for both environments. Degradation in the liquid medium leads to multiphase core–cortex morphology formation, while the environment with high partial pressure of water vapour provides homogeneous-like bulk degradation of the samples due to significantly different diffusion conditions on the liquid-polymer and water vapour saturated air-polymer interface. [Copyright &y& Elsevier]

The morphology and viscoelastic properties of newly prepared partially biodegradable polymeric blend based on polyamide 6 and commercially available co-polyester of polylactide, BioFlex®, were studied in this work. Observations by scanning electron microscopy and solvent extraction method, and rheological measurements were carried out for structural studies. Experimental data were compared with several semi-empirical models for determination of phase inversion concentration. The correlation between experimental data and models reveals the significant contribution of elasticity effect to interfacial adhesion between polyamide 6 and BioFlex, which seems to have influence on the phase inversion composition of the blends and co-continuous morphology formation. [ABSTRACT FROM AUTHOR]

Novel polymeric systems with antibacterial properties based on medical-grade polyvinyl chloride and antibiotics (Ampicillin, Minocycline, and Rifampicin) in the concentrations up to 1 wt% were prepared by thermoplastic compounding. Thermal stability of the antibiotics was corroborated by IR spectroscopy, X-ray diffraction, differential scanning calorimetry, and H nuclear magnetic resonance spectroscopy. The effect of chemical structure on mechanical properties of the prepared systems was determined by tensile testing measurements and correlated with optical microscopy observations. In vitro antibacterial properties of samples were determined by agar diffusion and adhesion test against Gram-negative and Gram-positive bacteria. Antibiotic release experiments in distilled water and physiological saline solution and follow-up detecting by Ultraviolet-Visible spectroscopy were carried out. A mathematical model was applied to evaluate the release kinetics of the antibiotics from prepared polymeric systems. The results show significant influence of antibiotic's chemical structure on all studied characteristics of the systems due to the various interactions with polyvinyl chloride matrix. [ABSTRACT FROM AUTHOR]

This study investigated the effect of natural antioxidants inherent to beetroot (Beta vulgaris var. Vulgaris) on the ageing of environmentally friendly plastics. Certain properties were examined in this context, comprising thermal, mechanical, and morphological properties. A visual evaluation of relevant changes in the given polymers (polylactide and polycaprolactone) was conducted during an ageing test in a UV chamber (45 °C, 70% humidity) for 720 h. The films were prepared by a casting process, in which samples with the extract of beetroot were additionally incorporated in a common filler (bentonite), this serving as a carrier for the extract. The results showed the effect of the incorporated antioxidant, which was added to stabilize the biodegradable films. Its efficiency during the ageing test in the polymers tended to exceed or be comparable to that of the reference sample. [ABSTRACT FROM AUTHOR]

Background: This research paper focuses on removing of arsenic from contaminated water via a nanofibrous polymeric microfiltration membrane, applied in prospective combination with an inorganic sorbent based on iron oxide hydroxide FeO(OH).Nanofibrous materials were prepared by electrospinning from polyurethane selected by an adsorption test. The chemical composition (FTIR), morphology (SEM, porometry) and hydrophilicity (contact angle) of the prepared nanostructured material were characterized. The process of eliminating arsenic from the contaminated water was monitored by atomic absorption spectroscopy (AAS). The adsorption efficiency of the nanofibrous material and the combination with FeO(OH) was determined, the level of arsenic anchorage on the adsorption filter was assessed by a rinsing test and the selectivity of adsorption in arsenic contaminated mineral water was examined.It was confirmed that the hydrophilic aromatic polyurethane of ester type PU918 is capable of capturing arsenic by complexation on nitrogen in its polymer chains. The maximum As removal efficiency was around 62 %. Arsenic was tightly anchored to the polymeric adsorbent. The adsorption process was sufficiently selective. Furthermore, it was found that the addition of even a small amount of FeO(OH) (0.5 g) to the nanofiber filter would increase the efficiency of As removal by 30 %.The presented results showed that an adsorption filter based on a polyurethane nanostructured membrane added with an inorganic adsorbent FeO(OH) is a suitable way for the elimination of arsenic from water. However, it is necessary to ensure perfect contact between the surface of the nanostructure and the filtered medium.Materials and methods: This research paper focuses on removing of arsenic from contaminated water via a nanofibrous polymeric microfiltration membrane, applied in prospective combination with an inorganic sorbent based on iron oxide hydroxide FeO(OH).Nanofibrous materials were prepared by electrospinning from polyurethane selected by an adsorption test. The chemical composition (FTIR), morphology (SEM, porometry) and hydrophilicity (contact angle) of the prepared nanostructured material were characterized. The process of eliminating arsenic from the contaminated water was monitored by atomic absorption spectroscopy (AAS). The adsorption efficiency of the nanofibrous material and the combination with FeO(OH) was determined, the level of arsenic anchorage on the adsorption filter was assessed by a rinsing test and the selectivity of adsorption in arsenic contaminated mineral water was examined.It was confirmed that the hydrophilic aromatic polyurethane of ester type PU918 is capable of capturing arsenic by complexation on nitrogen in its polymer chains. The maximum As removal efficiency was around 62 %. Arsenic was tightly anchored to the polymeric adsorbent. The adsorption process was sufficiently selective. Furthermore, it was found that the addition of even a small amount of FeO(OH) (0.5 g) to the nanofiber filter would increase the efficiency of As removal by 30 %.The presented results showed that an adsorption filter based on a polyurethane nanostructured membrane added with an inorganic adsorbent FeO(OH) is a suitable way for the elimination of arsenic from water. However, it is necessary to ensure perfect contact between the surface of the nanostructure and the filtered medium.Results: This research paper focuses on removing of arsenic from contaminated water via a nanofibrous polymeric microfiltration membrane, applied in prospective combination with an inorganic sorbent based on iron oxide hydroxide FeO(OH).Nanofibrous materials were prepared by electrospinning from polyurethane selected by an adsorption test. The chemical composition (FTIR), morphology (SEM, porometry) and hydrophilicity (contact angle) of the prepared nanostructured material were characterized. The process of eliminating arsenic from the contaminated water was monitored by atomic absorption spectroscopy (AAS). The adsorption efficiency of the nanofibrous material and the combination with FeO(OH) was determined, the level of arsenic anchorage on the adsorption filter was assessed by a rinsing test and the selectivity of adsorption in arsenic contaminated mineral water was examined.It was confirmed that the hydrophilic aromatic polyurethane of ester type PU918 is capable of capturing arsenic by complexation on nitrogen in its polymer chains. The maximum As removal efficiency was around 62 %. Arsenic was tightly anchored to the polymeric adsorbent. The adsorption process was sufficiently selective. Furthermore, it was found that the addition of even a small amount of FeO(OH) (0.5 g) to the nanofiber filter would increase the efficiency of As removal by 30 %.The presented results showed that an adsorption filter based on a polyurethane nanostructured membrane added with an inorganic adsorbent FeO(OH) is a suitable way for the elimination of arsenic from water. However, it is necessary to ensure perfect contact between the surface of the nanostructure and the filtered medium.Conclusions: This research paper focuses on removing of arsenic from contaminated water via a nanofibrous polymeric microfiltration membrane, applied in prospective combination with an inorganic sorbent based on iron oxide hydroxide FeO(OH).Nanofibrous materials were prepared by electrospinning from polyurethane selected by an adsorption test. The chemical composition (FTIR), morphology (SEM, porometry) and hydrophilicity (contact angle) of the prepared nanostructured material were characterized. The process of eliminating arsenic from the contaminated water was monitored by atomic absorption spectroscopy (AAS). The adsorption efficiency of the nanofibrous material and the combination with FeO(OH) was determined, the level of arsenic anchorage on the adsorption filter was assessed by a rinsing test and the selectivity of adsorption in arsenic contaminated mineral water was examined.It was confirmed that the hydrophilic aromatic polyurethane of ester type PU918 is capable of capturing arsenic by complexation on nitrogen in its polymer chains. The maximum As removal efficiency was around 62 %. Arsenic was tightly anchored to the polymeric adsorbent. The adsorption process was sufficiently selective. Furthermore, it was found that the addition of even a small amount of FeO(OH) (0.5 g) to the nanofiber filter would increase the efficiency of As removal by 30 %.The presented results showed that an adsorption filter based on a polyurethane nanostructured membrane added with an inorganic adsorbent FeO(OH) is a suitable way for the elimination of arsenic from water. However, it is necessary to ensure perfect contact between the surface of the nanostructure and the filtered medium. [ABSTRACT FROM AUTHOR]

This study investigates antibacterial polymer composites based on polypropylene as modified by caraway essential oil at various concentrations, the latter immobilized on a talc. The caraway essential oil is incorporated in the polypropylene by a thermoplastic processing method. Analysis of the morphology of the composites was carried out by scanning electron microscopy. The chemical composition of the caraway essential oil in addition to its efficiency of incorporation and release were evaluated by GC/MS and Pyrolysis-GC/MS techniques, respectively. Determination was made as to the influence of such incorporation on thermal and tensile properties of the samples, while antibacterial activity was evaluated through conducting disk diffusion tests and measurement with adherence to the ISO 22196:2011 standard. It was found that incorporating the caraway essential oil in the samples did not affect the homogeneity of the thermoplastic-processed composites at any studied concentration. Stress–strain analysis confirmed the plasticizing effect of the essential oil in the polypropylene matrix, in addition to which, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) analysis revealed that the prepared compositions with essential oil exhibited similar thermal properties to neat polypropylene. Results indicated significant antibacterial activity against Staphylococcus aureus and Escherichia coli at the concentration of essential oil of 4.9 ± 0.2 wt% and higher. [ABSTRACT FROM AUTHOR]

Hydrogels show potential in agriculture for overcoming issues associated with conventional fertilizers and irrigation. A combination of hydrogels and fertilizers would limit the loss of fertilizer and curb environmental impact, especially for nitrogen-based compounds, in addition to diminishing the frequency of irrigation. A set of renewable hydrogels, based on a mixture of whey proteins and alginic acid were developed as a soil conditioner and for sustained release of the urea fertilizer. Four separate formulations were prepared from different proteins at a polysaccharide ratio of 1%–10% w/w (with respect to protein content). The hydrogels were prepared by a heat-set process, applying calcium chloride as the cross-linking agent. The fertilizer was loaded into the hydrogel during the preparation stage to heighten loading efficiency. Investigation was made into the impact of alginic acid content on morphology, swelling behaviour - encompassing repeated swelling-drying cycles, and water retention in soil under different pH conditions. The loading capacity and release of urea from the hydrogels were studied, and the data processed in accordance with a mathematical model to discern any correlation between the structure of the hydrogel, the presence of alginic acid and the release mechanism. The results demonstrate how adding alginic acid promotes possible utilization of the whey protein hydrogel in agriculture. • Renewable hydrogels based on alginate and whey protein were prepared. • Correlations between alginic acid content and hydrogel properties were evaluated. • pH responsive swelling behavior. • Slow release of urea and high water holding capacity. • Promising alternative to commercial hydrogels based on synthetic polymers. [ABSTRACT FROM AUTHOR]

• DTPA-chitosan/PEO nanofibers were prepared. • Adsorption of Cu2+, Pb2+ and Ni2+ from water sources. • Pseudo-second order adsorption kinetics. • Maximal adsorption capacities for Cu2+, Pb2+ and Ni2+ ions are 177 mg g−1,142 mg g−1 and 56 mg g−1. Diethylenetriaminepentaacetic acid-modified chitosan/polyethylene oxide nanofibers (CS-DTPA/PEO NFs) were developed for enhanced heavy metal ion adsorption. These nanofibers were prepared by electrospinning, and their morphology and structure were investigated by scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR), respectively. The ability of CS-DTPA/PEO NFs to removing copper (Cu2+), lead (Pb2+) and nickel (Ni2+) ions from aqueous solutions was tested at room temperature. The effects of [DTPA]/[NH 2 molar ratio, pH and initial concentration of metal ions on their absorption capacity were investigated to optimize process conditions, using pseudo-first and apparent-second-order, Boyd and intraparticle diffusion models to determine the rate-limiting step of metal ions adsorption. In turn, Freundlich, Langmuir, Temkin and Dubinin-Radushkevich isotherm models were used to describe the experimental data. The results demonstrate a decrease in the ability of CS-DTPA/PEO NFs to adsorb metal ions in the following order: Cu2+>Pb2+>Ni2+. The adsorption equilibrium is established after 90 min from the first contact with solutions containing the metal ions, and data are described using the Langmuir isotherm model. The maximal adsorption capacities of CS-DTPA/PEO NFs for Cu2+ , Pb2+ and Ni2+ions were 177, 142, 56 mg g−1, respectively. The stability and reproducibility of CS-DTPA/PEO NFs were determined after five adsorption–desorption tests. [ABSTRACT FROM AUTHOR]

In this study, thin, polymeric films consisting of poly(vinyl alcohol) (PVA) and chitosan (Ch) with the addition of poly(hexamethylene guanidine) (PHMG) were successfully prepared. The obtained materials were analyzed to determine their physicochemical and biocidal properties. In order to confirm the structure of PHMG, nuclear magnetic resonance spectroscopy (1H NMR) was applied, while in the case of the obtained films, attenuated total reflectance infrared spectroscopy with Fourier transform (FTIR-ATR) was used. The surface morphology of the polymer films was evaluated based on atomic force microscopy. Furthermore, the mechanical properties, color changes, and thermal stability of the obtained materials were determined. Microbiological tests were performed to evaluate the biocidal properties of the new materials with and without the addition of PHMG. These analyses confirmed the biocidal potential of films modified by PHMG and allowed for comparisons of their physicochemical properties with the properties of native films. In summary, films consisting of PVA and PHMG displayed higher antimicrobial potentials against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria in comparison to PVA:Ch-based films with the addition of PHMG. [ABSTRACT FROM AUTHOR]