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At least 1,099 records · Page 61

Synthesis of Carboxyl-Rich Biosorbent by UV-Induced Graft Polymerization Method for High Efficiency Adsorption of Ce{sup 3+} from Aqueous Solution: Activation and Adsorption Mechanism

Developing a cost-effective and highly efficient sorbent for the recovery of rare-earth elements from aqueous solution is still an urgent need. In this study, a novel biosorbent, carboxyl-rich pine bark (CPB), was modified by UV-induced graft polymerization method to increase the carboxyl-containing functional groups and facilitate the adsorption of Ce{sup 3+}. The grafting process was examined by Fourier transform infrared (FTIR) spectroscopy and field emission scanning electron microscopy (FESEM), indicating that high-density carboxyl functional groups are present on the surface of pine bark and the grafting yield of surface polymer brushes reaches up to 128%. Interestingly, the maximum adsorption capacity of Ce{sup 3+} on CPB could reach up to 256.5 mg/g. The adsorption mechanism of Ce{sup 3+} by CPB has been determined by the adsorption models and x-ray photoelectron spectroscopy (XPS), which can be inferred from these results that the high performance of CPB is attributed to the surface coordination between Ce{sup 3+} and hydroxyl or carbonyl groups. This work suggests that engineered surface functional groups of biomass could have an opportunity for the development of high performance rare-earth element adsorbents.

54 ENVIRONMENTAL SCIENCES↗

Effects of Surface Modifications of Kraft Wood Pulp Cellulose Fibres on Improving the Mechanical Properties of Cellulose Fibre/Latex Composites

In this work, three composites with different contents (5, 10, and 15% w/w) of kraft pulp fibre were produced as reinforcing elements for natural latex matrix and the mechanical properties were evaluated. In order to improve the interfacial adhesion between the matrix and the reinforcing element, chemical modifications were carried out on the surface of the fibres using octanoyl and benzoyl chlorides as modifying agents. The extension of chemical modification of the fibres was visualized by the presence of absorption bands in the spectroscopy analyzes of the modified fibre in relation to the crude fibre (ester carbonyl 1700–1740 cm{sup −1}); in addition, the hydroxyl band was preserved, which indicates a modification of surface character. The modified fibres became more hydrophobic due to the decrease in surface energy and the change in the dispersive and polar components. An increase in the storage modulus was observed for the composites with surface-modified fibres, which agrees with the improved dispersion between the surface-modified fibres and the matrix verified by means of scanning electron microscopy images. The incorporation of fibres did not cause changes in the thermal properties of the composites.

36 MATERIALS SCIENCE↗

Chitosan/Polyaniline Conductive Blends for Developing Packaging: Electrical, Morphological, Structural and Thermal Properties

The present study aim to evaluate the development of electrical conducting blends made from the biodegradable polymer, chitosan (Cs), and polyaniline (PANI) doped with dodecylbenzene sulfonic acid dissolved in acid solution chitosan, to enable development of conductive and smart packages that help to monitor exposure conditions of food aimed to reduce food waste. Concentration of Cs is fixed (2%), and PANI (80, 100 mg mL{sup −1}) and glutaraldehyde (Glut) (0.625 × 10{sup −3} μL) concentrations are alter. Morphological (SEM), structural (FTIR, RAMAN), thermal (TGA) and electrical (Hall effect) properties are evaluate. Blends were predominantly negative carriers, with conductivity in order of 10{sup −1} S cm{sup −1}. Best formulations are those make without of Glut. Analyses show an interaction between components. FTIR show bands characteristic of benzene and quinoid rings of PANI, and RAMAN exhibit a band related to PANI’s protonation. TGA show maintenance of maximum degradation temperature of PANI. This results evidence maintenance of PANI’s conducting structures even after blends synthesis.

36 MATERIALS SCIENCE↗

Multidrug Core–Shell Bead: A System for Bacterial Infection Treatment in Fish

This study was developed to improve the durability and bioavailability of polymer matrix containing the antibacterial agent’s bacitracin (BAC), berberine (BER) and sodium nitroprusside (SNP), an ionotropic gelation method was successfully applied to prepare alginate/chitosan core–shell beads. The structure and properties of different core–shell beads were characterized by scanning electron microscopy (SEM), zeta potential, Fourier transform infrared spectroscopy (FTIR), thermal analysis (DSC), swelling tests, bioadhesive assay, release kinetic profile and antibacterial/antibacteriostatic activity in bacterial model. The morphology of beads was investigated by SEM, display relatively spherical shape and revealed rough surface was also observed the appearance of cracks probably caused by partial collapsing of the polymer network during drying. The diameter means particle size observed was around 1.04 ± 0.13 mm, the particles showed a neutral value, around + 0.305 mV. Using UV–Vis technique was observed a high entrapment efficiency of compounds BAC, BER and SNP (> 95%) in the alginate/chitosan core–shell beads. As demonstrated, there is increase in the swelling degree in pH 6.2. The drug release profile showed a pH-dependent release kinetics. At pH 5.0 the most suitable kinetic model is Higuchi, at pH 6.2 a zero-order model is observed, while at pH 7.4 the Korsmeyer–Peppas model present a good fit. The presence of compounds on beads was confirmed using FTIR analyses, and the results indicated that there is no interaction between drugs and vehicle used in the formulation. We can consider after DSC analysis that beads containing BAC, BER and SNP are thermally more stable than separate formulations having the characteristics required for application at room temperature. The release system produced has physical characteristics that allow the storage of the drugs for long periods of time maintaining their chemical and pharmacological properties unchanged. The percentage of adhesion displayed value of 66%, that indicates the improvement in adherence time on the absorbing surfaces to improves drug bioavailability and effectiveness of compounds. In this study is displayed the additive effect between BAC, BER and SNP shown the potential application of compound combinations as an efficient, novel therapeutic tool for antibiotic-resistant bacterial infections. These results indicate that the proposed strategy improves drug bioavailability and effectiveness of compounds in the treatment of fish.

36 MATERIALS SCIENCE↗

A New Study on Characterization and Properties of Natural Fibers Obtained from Olive Tree (Olea europaea L.) Residues

Nowadays, fibers extracted from natural resources have a wide range of promising applications, including the prospect to be used as reinforcing material in polymer composites. In this context, the purpose of this study has been to extract fibers from different parts of the olive tree (leaves, small and large branches) and characterize their physico-chemical, thermal, and morphological properties using advanced equipment. Olive leaf (OL) fiber showed asymmetrical size distribution, as compared to those extracted from small olive branches (OSS), and big olive branches (OBS). The OL fiber exhibited 64.1% crystallinity, which is lower than that of the OSS fiber—with 65.4% crystallinity. Thermal analysis revealed that the OBS and OSS fibers are more thermally stable, compared to the OL fibers. The obtained results concluded that olive tree fibers can be suitable for being used as reinforcement material to develop polymer composites for various lightweight applications.

36 MATERIALS SCIENCE↗

Synthesis of Melanin Mediated Silver Nanoparticles from Aeromonas sp. SNS Using Response Surface Methodology: Characterization with the Biomedical Applications and Photocatalytic Degradation of Brilliant Green

Melanin is ubiquitous in nature and has wide applications in cosmetics, agriculture, and medicine. The synthesized melanin from bacterium Aeromonas sp. SNS was further used as capping and reducing agents for synthesis of silver nanoparticles (AgNPs). The influence of the experimental parameters (AgNO{sub 3}, melanin concentrations, and temperature) and their interactions on the nanoparticle synthesis was optimized using response surface methodology (RSM). The Central Composite Design (CCD) with three independent variables was optimized for the effective synthesis of AgNPs. The optimized synthesis of AgNPs was achieved at the shortest time of 14.12 h in the presence of 2.62 mM AgNO{sub 3}, and 32.30 µg ml{sup −1} melanin concentration at 54.86 °C temperature. The synthesized AgNPs were characterized by means of UV–visible spectroscopy, FTIR, SEM, TEM, and PSD respectively. The AgNPs exhibited excellent antimicrobial activity against human and food-related pathogens. These AgNPs also have strong antioxidant potential which was estimated by DPPH, DMPD and FRAP radical scavenging assays. The 92.62% photocatalytic degradation of 250 PPM brilliant green was observed in 120 min. The present finding accelerates the melanin associated AgNPs could be used in the cosmetic and pharmaceutical industries as well as in textile industries as they have superior antimicrobial, antioxidant, and photocatalytic activity.

36 MATERIALS SCIENCE↗

The Taste of Waste: The Edge of Eggshell Over Calcium Carbonate in Acrylonitrile Butadiene Rubber

Rubber technology experiences a new age by the use of biowaste or natural fillers. In this regard, taking properties of reinforcing agents from biowaste fillers remains as the challenging matter. Chicken eggshell (ES) biowaste has recently been introduced to substitute calcium carbonate (CaCO{sub 3}) duo to its superior properties and low price. In this work, composites based on acrylonitrile butadiene rubber (NBR) reinforced with ES and CaCO{sub 3} microfillers at various loading levels were prepared and characterized. To improve the interactions between fillers and the NBR matrix, ES and CaCO{sub 3} were surface-functionalized using a terpolymer, namely poly(vinyl 2-pyrrolidone-co-maleic acid-co-acrylic acid). Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) were used to characterize the modified fillers. The incorporation of the functionalized fillers resulted in a significant rise in the maximum torque according to the rheometric measurements. The Young’s modulus of the ES-based and CaCO{sub 3}-based compounds showed a mild improvement over a wide range of filler contents. The elongation at break of the NBR composites, however, was dependent on the filler content. This work provides exciting opportunities for the design of novel and innovative coupling agents to be used in rubber applications.

36 MATERIALS SCIENCE↗

Magnetic Nanoparticles Impregnated, Cross-Linked, Porous Chitosan Microspheres for Efficient Adsorption of Methylene Blue from Pharmaceutical Waste Water

The study demonstrates the preparation of MnFe{sub 2}O{sub 4} impregnated chitosan-microspheres (CMMS) as adsorbents for efficient removal of cationic thiazine dye, methylene blue. A facile approach with great economic and technical advantages to obtain highly crystalline manganese ferrite nanoparticles by solution combustion method is accounted. CMMS were characterized and evaluated for MB adsorption using linear forms of Freundlich and Langmuir adsorption isotherms, pseudo-first order, pseudo-second order and Elovich kinetic models. Application of CMMS to pharmaceutical waste, desorption of MB and reusability of CMMS are reported. Significantly, MB concentration in treated real sample was reduced by ~ 18 times to that of initial concentration. Graphic Abstract: .

36 MATERIALS SCIENCE↗

Investigation into the Role of Surface Modification of Cellulose Nanocrystals with Succinic Anhydride in Dye Removal

Herein, the effect of surface modification of cellulose nanocrystals (CNC) on the sorption of dyes from waste textile effluent (methylene blue as a model) was achieved. The esterification of the isolated CNC from wood sawdust by acid hydrolysis was performed through melting with succinic anhydride (SA). At using 1:3–1:9 as the feeding ratios of CNC to SA, the succinylated CNC (CNC-SA) was obtained with degree of substitution of 1.6–2.2 and carboxylic content of 286.8–381.7 mmol/kg. Both of diameter size and zeta potential of the prepared CNC-SA were gradually enlarged by increasing the reactant feed ratio, indicating the successful modification of CNC surface with highly stable particles via increasing the negative charges on the outer surface. FTIR and XRD affirmed the change in the chemical structure as well as crystallinity of CNC after succinylation reaction. The prepared succinylated CNC was applied in the removal of methylene blue (MB) dye and the data showed that the sorption capacity is a direct proportional linear relation with the contents of carboxylic group. Within 120 min contact time, the sorption capacity was enlarged from 64.1 mg/g for CNC to 84.1 mg/g for CNC-SA3. The sorption data was fitted well to the first order kinetic model. Due to the esterification, the rate of sorption reaction is accelerated by double factor. These findings will maximize the benefit of esterified CNC in water treatment.

36 MATERIALS SCIENCE↗

Cu(II) Sorption Performance of Novel Chitosan/Ter-(vinyl pivalate-maleic anhydride-N-tert-butylacrylamide) Microcapsules

In this study, first, the ter-polymerization reaction between vinyl pivalate (VP), maleic anhydride (MA), and N-tert-butylacrylamide (NTBA) was done in inert atmosphere (N{sub 2}). FT-IR and {sup 1}HNMR spectroscopy was applied to study the chemical composition of the obtained ter-polymers. MA content of the ter-polymers was determined by following the chemical titration method. Second, novel chitosan/ter-(vinyl-pivalate-maleic-anhydride-N-tert-butylacrylamide) microcapsules were synthesized. In microcapsule production, chitosan polymer served as a matrix for acrylamide ter-polymers with four different molar ratios. The microcapsules were characterized by FT-IR and SEM analyses. Cu(II) sorption efficiency of the microcapsules were tested at different pH levels, temperature, sorbent dosage, and metal ion concentration. Comparison with blank chitosan microbeads revealed that incorporation of acrylamide ter-polymers into the cross-linked chitosan matrix increased the metal sorption. Sorption capacities of the sorbents were recorded; blank chitosan microbeads: 67.03 mg g{sup −1}, and chitosan/acrylamide ter-polymer microcapsules: in range of 75.39–98.64 mg g{sup −1}. The findings demonstrated chitosan/acrylamide ter-polymer microcapsules can be utilized in sorption of Cu(II) ions in water treatment.

36 MATERIALS SCIENCE↗

Effect of Natural and Accelerated Aging on the Mechanical Performance of a Composite Based on Recycled Multilayer Carton

A composite elaborated from waste material was studied for its proposed use as a wood plastic composite. Multilayer food cartons and recycled high density polyethylene were used for the elaboration of laminates, in a proportion of 55% and 45% volume fraction, respectively. The samples were subjected to an aging in an accelerated weathering (AW) chamber for 0, 500, 1000 and 2000 h with UVB radiation, temperature and humidity cycles. Samples exposed to natural weathering (NW) for 0, 1300, 2600 and 5200 h, in a warm sub-humid environment were also studied, the aim being to elucidate a correlation of the useful lifespan of the material. In both cases, after the exposure, three-point bend tests were performed to evaluate the effect on the mechanical properties. The analysis of the degradation process was carried out by infrared spectroscopy, indicating that the AW and NW samples showed deterioration of the material in different proportions. By mean of thermal analysis, it was possible to associate the degradation with the appearance and/or growth of the endothermic peaks, showing a variation in the melting temperature as the time of exposure to AW and NW increased, resulting in a change in the crystallinity percentage. The modulus of rupture (MOR) and the flexural modulus of elasticity decreased by 20% in samples subjected to AW for 2000 h; while in the samples exposed to NW, required of 5200 h to obtain a reduction of 16% in the MOR.

36 MATERIALS SCIENCE↗

Physicochemical, Microstructural and Thermal Characterization of Chitosan from Blue Crab Shell Waste and Its Bioactivity Characteristics

The aim of the present study was to characterize the chitosan synthesized from blue crab (Callinectes sapidus, Rathbun, 1986) shell waste and to investigate its physicochemical and microstructural analyses as well as its antioxidant and antibacterial potentials. Microstructural and elemental characterization of the synthesized and commercial chitosan powders were performed using fourier transform infra-red spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy. Thermal analysis were done using thermogravimetric analysis. Antioxidant and antimicrobial analysis were done using by DPPH (1,1-diphenyl-2-picrylhydrazyl) free radical scavenging assay and agar well diffusion assay, respectively. The yield of the synthesized chitosan was calculated as 7.47% with moisture and ash contents of 0.151 ± 0.0025% and 0.19 ± 0.01%, respectively. Synthesized chitosan demonstrated the values of degree of deacetylation (71%), water (620.029 ± 52.59%) and fat (437.93 ± 15.92%) binding capacities, solubility (94.15 ± 2.84%), viscosity (463.25 ± 13.10 cPs) and whiteness (90.23 ± 0.27%). Antioxidant activity of synthesized chitosan was found to be moderate (55.30 ± 5.05%) when compared to ascorbic acid standard (87.61 ± 1.34). Chitosan obtained from blue crab shell also showed moderate antibacterial activity against Staphylococcus aureus and Escherichia coli. The findings of the study indicated that blue crab shell waste might be a potentially effective biopolymer source for commercial applications especially in food industry.

36 MATERIALS SCIENCE↗

Abiotic Hydrolysis and Compostability of Blends Based on Cassava Starch and Biodegradable Polymers

When associated with polymer blends, starch may improve the biodegradability and compostability of other materials. The objectives of this work were to evaluate the abiotic hydrolysis and the composting process of films obtained from polymer blends between thermoplastic starch (TPS) and three other biodegradable polymers: poly[(butylene adipate)- co -(terephthalate)] (PBAT), poly(lactic acid) (PLA) and polyvinyl alcohol (PVA). PVA/TPS stood out as the most homogeneous blend and the one that showed the highest weight loss, with 46.21% of its initial weight remaining after abiotic hydrolysis tests. On the other hand, PBAT/TPS and PLA/TPS underwent more drastic and rapid degradation during composting in contrast to PVA/TPS. They became very fragmented after 21 days of composting, while the PVA/TPS was visually modified but remained unbroken until day 70. No blend sample exerted negative effects on the quality of the compost.

36 MATERIALS SCIENCE↗

Investigation of Thermoplastic Polyurethanes Synthesized via Two Different Prepolymers

The man aim of this work was to investigate the effect of the molecular weight of polyols, mixture of prepolymers, and [NCO]/[OH] molar ratio used during the prepolymer chain extending step on the chemical structure, thermomechanical and mechanical properties, and thermal stability of thermoplastic poly(ether-urethane)s In this work thermoplastic poly(ether-urethane)s were synthesized by using polyols with a various molecular weight, 4,4′-diphenylmethane diisocyanate and bio-based glycol. Materials were obtained by a two-step method. The tests were carried out for polyurethanes obtained from a mixture of prepolymers and for reference samples. In the case of materials obtained with using mixture of prepolymers, the ratio of both prepolymers was determined on 50/50 weight percent. Soft segments of materials prepared with using mixture consist of two different polyols. The chemical structure was analyzed using FTIR spectroscopy. The Gaussian deconvolution technique was used to study the hydrogen bonding as well as to decompose carbonyl region of three peaks in various TPUs. The thermal degradation behavior was investigated by using thermogravimetric analysis at heating rates of 10 °C/min. It was confirmed that the mixture of prepolymers has an effect of the degree of phase separation, thermal stability and selected properties of synthesized thermoplastic poly(ether-urethane)s.

36 MATERIALS SCIENCE↗

Soybean Oil Modified Bio-based Poly(vinyl alcohol)s via Ring-Opening Polymerization

In this paper, a simple method to modify the poly(vinyl alcohol) (PVA) through ring-opening reaction of epoxidized soybean oil (ESBO), catalyzed by hydrochloric acid is reported. The effect of ESBO loading ratio, in terms of mole (PVA/ESBO (n/n) = 1:0.5; 1:1 and 1:1.5) in the reaction medium, on the biodegradable, wettability and thermal properties of final PVA-SBO films is systematically investigated, comparing with PVA. The formation of PVA-SBOs is structurally confirmed by Fourier transform infrared (FT-IR) spectroscopy, whereas their wettability and thermal properties are studied by water contact angle (WCA) measurement, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC), respectively. The obtained PVA-SBOs with higher ESBO loading exhibit both improved thermal properties and higher hydrophobic characteristic compared to others. Furthermore, biodegradability of resulting PVA-SBOs is also investigated by enzymatic degradation experiments. It is determined that around 34% of PVA is degraded by enzymatic experiments after 30 days and PVA-SBO with lower ESBO loading is more degraded than others with around 52%. Consequently, some experimental results are presented to indicate that PVA-SBOs are encouraging materials for diverse applications and their extensions can be good candidate for reducing the environmental problem and consumption of petroleum resources.

36 MATERIALS SCIENCE↗

N-Silylated Benzothiazolium Dye as a Coupling Agent for Polylactic Acid/Date Palm Fiber Bio-composites

This work proposes a benzothiazole derivative bearing a silane moiety as a new coupling agent for polylactic acid (PLA) reinforced by date palm fibers (DPFs). The bio-composites are prepared by solution blending followed by melt compounding. From the samples produced, a complete characterization is performed including morphological, mechanical and thermal properties as a function of fiber content. The results show that the proposed fiber treatment is an easy and effective method to improve the interfacial properties and fiber dispersion leading to better material performance. For example, the addition of only 1 wt% of the dye–IPTMS to the bleached DPF not only improved the thermal stability of the biocomposites, but also led to a significant increase of the Young’s modulus at 7 wt% and higher torsion modulus up to 5 wt% (optimum value).

36 MATERIALS SCIENCE↗

Effect of Synthesis Approaches and Morphological Properties on Dielectric Enhancement and Microwave Absorption of Fe{sub 3}O{sub 4}/PANI Nanocomposites

In the present work, Fe{sub 3}O{sub 4} spherical (Fe{sub 3}O{sub 4}-cop) and raspberry-like (Fe{sub 3}O{sub 4}-hyd) nanoparticles were synthesized via co-precipitation and hydrothermal routes, respectively. Fe{sub 3}O{sub 4}/polyaniline (PANI) nanocomposites were prepared by in situ oxidative polymerization of aniline monomer in the presence of the Fe{sub 3}O{sub 4} materials. Characterization of the nanocomposites by XRD, FT-IR, FESEM, and TEM techniques revealed a core/shell structure for Fe{sub 3}O{sub 4}-hyd/PANI, unlike the PANI blocks with embedded Fe{sub 3}O{sub 4} and γ-Fe{sub 2}O{sub 3} observed in Fe{sub 3}O{sub 4}-cop/PANI composites. The larger and pure magnetite nanoparticles produced with the hydrothermal process and the respective nanocomposite with PANI possess higher magnetization and coercivity values, according to the magnetic investigation with VSM. Moreover, according to the electromagnetic characterization in the X-band, the Fe{sub 3}O{sub 4}-hyd/PANI nanocomposite exhibits the highest complex permittivity level, as a consequence of increased interfacial polarization in the Fe{sub 3}O{sub 4}-hyd/PANI system. On this account, reflection loss measurements have shown the superior microwave absorption capability of Fe{sub 3}O{sub 4}-hyd/PANI composite, compared with Fe{sub 3}O{sub 4}-cop/PANI, with a measured maximum of −31.28 dB at 8.5 GHz for 3.5 mm layer thickness.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Synthesis and Characterization of Nickel-Substituted Cobalt Ferrite Nanoparticles Using Sol–Gel Auto-combustion Method

In the present work, Co{sub 1−x}Ni{sub x}Fe{sub 2}O{sub 4} (x = 0.02, 0.04, and 0.06 M) is prepared by sol–gel auto-combustion method and its structural, functional, magnetic, and morphological characteristics are analyzed. The peaks corresponding to the plane observed from XRD matches with JCPDS data of CoFe{sub 2}O{sub 4} (22-1086) and NiFe{sub 2}O{sub 4} (10-0325). It is noted that the average crystallite size decreases from 31 to 27 nm when the nickel concentration increases from 0.02 to 0.06 M, indicative of the incorporation of Ni{sup 2+} ion in the cobalt ferrite lattice. FTIR analysis shows the presence of M↔O vibration at the tetrahedral and octahedral sites. Micro - Raman spectroscopy shows the stretching vibrations at 486.87 cm{sup − 1} (E{sub g}) and 696.96 cm{sup − 1} (A{sub 1g}), which are the characteristic vibrations of spinel ferrites. Magnetic studies show the variation in saturation magnetization (M{sub S} = 20.25, 9.41, 18.5 emu/g.) and coercivity (H{sub C} = 746.06, 953.03, 885.59 Oe) when the concentration of Ni{sup 2+} ion increases from 0.02 to 0.06 M. The prepared nanoparticles show a ferromagnetic nature which is attributed to the creation of an antiparallel spin and the magnetic moment created by the cation at tetrahedral and octahedral sites. The surface morphology of samples is imaged by a field emission scanning electron microscope.

77 NANOSCIENCE AND NANOTECHNOLOGY↗