Properties of Polypropylene Nanocomposites Containing Silver Nanoparticles

2007 ◽  
Vol 7 (11) ◽  
pp. 3990-3994 ◽  
Author(s):  
Myung Wook Jang ◽  
Ju-Young Kim ◽  
Kyo Jin Ihn
Keyword(s):  
Mechanical Properties ◽  
Silver Nanoparticles ◽  
Self Assembly ◽  
Synthetic Method ◽  
Colloidal Solutions ◽  
Nano Structures ◽  
Polypropylene Nanocomposites ◽  
Vis Spectroscopy ◽  
Silver Nanocomposites ◽  
Hydrophilic Domain

Silver/polypropylene (PP) nanocomposites containing silver nanoparticles smaller than 10 nm were prepared using a new synthetic method. AgNO3 crystals were dissolved into hydrophilic domain of polyoxyethylene maleate-based surfactant (PEOM), which gives self-assembly nano-structures. The AgNO3 in the nano-domains of PEOM was reduced by NaBH4 to form nanoparticles. The colloidal solutions with silver nanoparticles were diluted with ethanol and were mixed with PP pellets. Silver nanocomposites were prepared by extrusion compounding process after drying the pellets. Contents of silver nanoparticles dispersed within PP resin were changed from 100 to 1000 ppm. Formation of silver nanoparticles within PP was confirmed by UV-Vis spectroscopy and TEM. Size and distribution of dispersed silver nanoparticles were also measured by TEM. Silver/PP nanocomposites films showed not only improved thermal stability but also increased mechanical properties compared to neat PP film. Tensile properties of PP nanocomposites were largely improved compared with neat PP resin, and elongation increased also by 175% for the nanocomposites containing 1000 ppm silver nanoparticles.

scholarly journals Green Synthesis of Silver Nanoparticles in the Presence of Polysaccharide: Optimization and Characterization

2020 ◽  
Vol 2020 ◽  
pp. 1-10 ◽  
Author(s):  
Margarita I. Skiba ◽  
Victoria I. Vorobyova ◽  
Alexander Pivovarov ◽  
Natalya P. Makarshenko
Keyword(s):  
Silver Nanoparticles ◽  
Sodium Alginate ◽  
Xrd Analysis ◽  
Face Centered Cubic ◽  
Colloidal Solutions ◽  
Ag Nps ◽  
Sem Images ◽  
Spherical Powder ◽  
Stabilizing Agent ◽  
Vis Spectroscopy

The process of obtaining aqueous solutions of silver nanoparticles with the use of a low-temperature nonequilibrium contact plasma and stabilizing agent—polysaccharide (sodium alginate)—has been examined. The synthesized Ag NPs were characterized by using UV-Vis spectroscopy, dynamic light scattering (DLS), scanning electron microscope (SEM), and XRD analysis. The effect of concentration of Ag+, sodium alginate, duration of processing by plasma discharge, and pH of liquid on the production of silver nanoparticles has been studied. The results demonstrated that synthesis provides the formation of silver nanoparticles for investigated concentrations of Ag+ (0.3-3.0 mmol/l) and 5.0 g/l Na-Alg (pH=7–10) within 1–5 minutes. From the SEM images, the silver nanoparticles are found to be almost spherical. Powder XRD results reveal that Ag nanoparticles have a face-centered cubic crystal structure. Zeta potential of plasma-chemically obtained colloidal solutions at various concentrations of Ag+ ions and stabilizing agent varies from −32.8 to −39.3 mV, indicating the moderate stability of synthesized nanoparticles.

scholarly journals SYNTHESIS AND CHARACTERIZATION OF SILVER NANOPARTICLES

2019 ◽  
Vol 31 (3) ◽  
pp. 643-646
Author(s):  
Leon Stojanov ◽  
Nese Salih ◽  
Valentin Mirceski
Keyword(s):  
Silver Nanoparticles ◽  
Pure Water ◽  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Localized Surface Plasmon ◽  
Colloidal Solutions ◽  
Vis Spectroscopy ◽  
Voltammetric Detection ◽  
Anodic Stripping ◽  
Redox Agents

Silver nanoparticles have been formed with two different methods: by reduction of Ag+ ions from AgNO3 aqueous solution and reduction of Ag+ ions obtained by electrolysis in a pure water by using ultrapure Ag electrode. Glutathione and ascorbic acid have been used as reductive redox agents. The preparation has been conducted by mixing aqueous solutions of reactants at different concentrations. Formation of colloidal solutions containing silver nanoparticles has been confirmed by electrochemical, spectroscopic, and microscopic techniques. By applying UV-Vis spectroscopy the formation of nanoparticles has been supported with the localized surface plasmon resonance absorption peak at 350 nm. The morphology and dimensions of the formed silver nanoparticles have been studied by inspecting microphotographs collected by atomic force microscopy. The decrease of the concentration of the free Ag+ ions following the reduction with the reductants has been measured by anodic stripping voltammetry using square-wave voltammetry as a potential modulation form. As a result of addition of reductive agents, a colloid of silver nanoparticles is formed, which is not prone to detection with anodic stripping voltammetry. The problem was circumvented by using an excess of glutathione, causing adsorptive accumulation of silver nanoparticles at the electrode surface, thus enabling anodic oxidation and voltammetric detection of silver particles.

scholarly journals Rapid Green Synthesis and Characterization of Silver Nanoparticles Arbitrated by Curcumin in an Alkaline Medium

Molecules ◽  
2019 ◽  
Vol 24 (4) ◽  
pp. 719 ◽  
Author(s):  
Muhammad Khan ◽  
Kamyar Shameli ◽  
Awis Sazili ◽  
Jinap Selamat ◽  
Suriya Kumari
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Green Synthesis ◽  
Alkaline Medium ◽  
Research Area ◽  
Crystallographic Structure ◽  
Face Centered Cubic ◽  
Colloidal Solutions ◽  
Ag Nps ◽  
Vis Spectroscopy

Green synthesis of silver nanoparticles is desirable practice. It is not only the required technique for industrial and biomedical purposes but also a promising research area. The aim of this study was to synthesize green curcumin silver nanoparticles (C-Ag NPs). The synthesis of C-Ag NPs was achieved by reduction of the silver nitrate (AgNO3) in an alkaline medium. The characterizations of the prepared samples were conducted by ultraviolet visible (UV-vis) spectroscopy, powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) and zeta potential (ZP) analyses. The formation of C-Ag NPs was evaluated by the dark color of the colloidal solutions and UV-vis spectra, with 445 nm as the maximum. The size of the crystalline nanoparticles, recorded as 12.6 ± 3.8nm, was confirmed by HRTEM, while the face-centered cubic (fcc) crystallographic structure was confirmed by PXRD and SAED. It is assumed that green synthesized curcumin silver nanoparticles (C-Ag NPs) can be efficiently utilized as a strong antimicrobial substance for food and meat preservation due to their homogeneous nature and small size.

Preparation of Silver Nanoparticles Having Low Melting Temperature Through a New Synthetic Process without Solvent

2007 ◽  
Vol 7 (11) ◽  
pp. 3805-3809 ◽  
Author(s):  
Nam Hee Kim ◽  
Ju-Young Kim ◽  
Kyo Jin Ihn
Keyword(s):  
Differential Scanning Calorimetry ◽  
Silver Nanoparticles ◽  
Melting Temperature ◽  
Synthetic Method ◽  
Silver Particles ◽  
Scanning Calorimetry ◽  
Synthetic Process ◽  
Silver Salts ◽  
Nanoparticle Sizes ◽  
Hydrophilic Domain

This study presents a new synthetic method of silver nanoparticles using a novel polyoxyethylene maleate-based surfactant (PEOM). Unlike conventional process using large amount of a solvent to dissolve silver salts, large amount of silver salts (AgNO3) can be dissolved and stabilized by our surfactant without solvent. Silver salts can be dissociated within PEOM by the formation of charge complex between hydrophilic-COOH segments and Ag+NO3−, resulting in formation of self-assembled microstructures which acting as a nano-reactor and stabilizer. After reduction using NaBH4, uniform sized silver nanoparticles were formed in the hydrophilic domain of PEOM. Silver contents in the colloids were changed by 0.5∼3 wt%. Distribution of silver nanoparticle sizes was investigated by using TEM and XRD. Melting temperature of silver nanoparticles was measured by differential scanning calorimetry, which depends upon the particle size of silver nanoparticles. The lowest melting temperature of 112° was measured from 3.5 nm average-sized silver particles.

Green synthesis of mixed metallic nanoparticles using room temperature self-assembly

2017 ◽  
Vol 13 (2) ◽  
pp. 4671-4677 ◽  
Author(s):  
A. M. Abdelghany ◽  
A.H. Oraby ◽  
Awatif A Hindi ◽  
Doaa M El-Nagar ◽  
Fathia S Alhakami
Keyword(s):  
Self Assembly ◽  
Metallic Nanoparticles ◽  
Room Temperature ◽  
Bimetallic Nanoparticles ◽  
Reduction Process ◽  
Nano Particles ◽  
Nano Structure ◽  
Small Shift ◽  
Molar Ratios ◽  
Vis Spectroscopy

Bimetallic nanoparticles of silver (Ag) and gold (Au) were synthesized at room temperature using Curcumin. Reduction process of silver and gold ions with different molar ratios leads to production of different nanostructures including alloys and core-shells. Produced nanoparticles were characterized simultaneously with FTIR, UV/vis. spectroscopy, transmission electron microscopy (TEM), and Energy-dispersive X-ray (EDAX). UV/vis. optical absorption spectra of as synthesized nanoparticles reveals presence of surface palsmon resonance (SPR) of both silver at (425 nm) and gold at (540 nm) with small shift and broadness of gold band after mixing with resucing and capping agent in natural extract which suggest presence of bimetallic nano structure (Au/Ag). FTIR and EDAX data approve the presence of bimetallic nano structure combined with curcumin extract. TEM micrographs shows that silver and gold can be synthesized separately in the form of nano particles using curcumin extract. Synthesis of gold nano particles in presence of silver effectively enhance and control formation of bi-metallic structure.

scholarly journals Silver Nanoparticles Functionalized by Fluorescein Isothiocyanate or Rhodamine B Isothiocyanate: Fluorescent and Plasmonic Materials

2021 ◽  
Vol 11 (6) ◽  
pp. 2472
Author(s):  
Ilaria Fratoddi ◽  
Chiara Battocchio ◽  
Giovanna Iucci ◽  
Daniele Catone ◽  
Antonella Cartoni ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Transient Absorption ◽  
Fluorescein Isothiocyanate ◽  
Dye Molecules ◽  
Chemical Surface ◽  
Vis Spectroscopy ◽  
Rhodamine B Isothiocyanate ◽  
Fluorescent Molecules

This paper presents the synthesis of silver nanoparticles (AgNPs) functionalized with fluorescent molecules, in particular with xanthene-based dyes, i.e., fluorescein isothiocyanate (FITC, λmax = 485 nm) and rhodamine B isothiocyanate (RITC, λmax = 555 nm). An in-depth characterization of the particle–dye systems, i.e., AgNPs–RITC and AgNPs–FITC, is presented to evaluate their chemical structure and optical properties due to the interaction between their plasmonic and absorption properties. UV–Vis spectroscopy and the dynamic light scattering (DLS) measurements confirmed the nanosize of the AgNPs–RITC and AgNPs–FITC. Synchrotron radiation X-ray photoelectron spectroscopy (SR-XPS) was used to study the chemical surface functionalization by structural characterization, confirming/examining the isothiocyanate–metal interaction. For AgNPs–RITC, in which the plasmonic and fluorescence peak are not superimposed, the transient dynamics of the dye fluorescence were also studied. Transient absorption measurements showed that by exciting the AgNPs–RITC sample at a wavelength corresponding to the AgNP plasmon resonance, it was possible to preferentially excite the RITC dye molecules attached to the surface of the NPs with respect to the free dye molecules in the solution. These results demonstrate how, by combining plasmonics and fluorescence, these AgNPs can be used as promising systems in biosensing and imaging applications.

scholarly journals Nanostructure, Self-Assembly, Mechanical Properties, and Antioxidant Activity of a Lupin-Derived Peptide Hydrogel

Biomedicines ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 294
Author(s):  
Raffaele Pugliese ◽  
Anna Arnoldi ◽  
Carmen Lammi
Keyword(s):  
Mechanical Properties ◽  
Antioxidant Activity ◽  
Self Assembly ◽  
Antioxidant Activities ◽  
Functional Materials ◽  
Cd Spectroscopy ◽  
Beneficial Effects ◽  
Naturally Occurring ◽  
New Research ◽  
Peptide Hydrogel

Naturally occurring food peptides are frequently used in the life sciences due to their beneficial effects through their impact on specific biochemical pathways. Furthermore, they are often leveraged for applications in areas as diverse as bioengineering, medicine, agriculture, and even fashion. However, progress toward understanding their self-assembling properties as functional materials are often hindered by their long aromatic and charged residue-enriched sequences encrypted in the parent protein sequence. In this study, we elucidate the nanostructure and the hierarchical self-assembly propensity of a lupin-derived peptide which belongs to the α-conglutin (11S globulin, legumin-like protein), with a straightforward N-terminal biotinylated oligoglycine tag-based methodology for controlling the nanostructures, biomechanics, and biological features. Extensive characterization was performed via Circular Dichroism (CD) spectroscopy, Fourier Transform Infrared spectroscopy (FT-IR), rheological measurements, and Atomic Force Microscopy (AFM) analyses. By using the biotin tag, we obtained a thixotropic lupin-derived peptide hydrogel (named BT13) with tunable mechanical properties (from 2 to 11 kPa), without impairing its spontaneous formation of β-sheet secondary structures. Lastly, we demonstrated that this hydrogel has antioxidant activity. Altogether, our findings address multiple challenges associated with the development of naturally occurring food peptide-based hydrogels, offering a new tool to both fine tune the mechanical properties and tailor the antioxidant activities, providing new research directions across food chemistry, biochemistry, and bioengineering.

scholarly journals Green synthesis of silver nanoparticles: Characterization and its potential biomedical applications

2021 ◽  
Vol 10 (1) ◽  
pp. 412-420
Author(s):  
Mona S. Alwhibi ◽  
Dina A. Soliman ◽  
Manal A. Awad ◽  
Asma B. Alangery ◽  
Horiah Al Dehaish ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Aloe Vera ◽  
Inhibition Zone ◽  
Biologically Active ◽  
Noble Metal Nanoparticles ◽  
Biological Synthesis ◽  
Ag Nps ◽  
Mouse Melanoma ◽  
Therapeutic Benefits ◽  
Vis Spectroscopy

Abstract In recent times, research on the synthesis of noble metal nanoparticles (NPs) has developed rapidly and attracted considerable attention. The use of plant extracts is the preferred mode for the biological synthesis of NPs due to the presence of biologically active constituents. Aloe vera is a plant endowed with therapeutic benefits especially in skincare due to its unique curative properties. The present study focused on an environmental friendly and rapid method of phytosynthesis of silver nanoparticles (Ag-NPs) using A. vera gel extract as a reductant. The synthesized Ag-NPs were characterized by transmission electron microscopy (TEM), UV-Vis spectroscopy, Fourier transform infrared (FTIR), and dynamic light scattering (DLS). TEM micrographs showed spherical-shaped synthesized Ag-NPs with a diameter of 50–100 nm. The UV-Vis spectrum displayed a broad absorption peak of surface plasmon resonance (SPR) at 450 nm. The mean size and size distribution of the formed Ag-NPs were investigated using the DLS technique. Antibacterial studies revealed zones of inhibition by Ag-NPs of A. vera (9 and 7 mm) against Pseudomonas aeruginosa and Escherichia coli, respectively. Furthermore, the antifungal activity was screened, based on the diameter of the growth inhibition zone using the synthesized Ag-NPs for different fungal strains. Anticancer activity of the synthesized Ag-NPs against the mouse melanoma F10B16 cell line revealed 100% inhibition with Ag-NPs at a concentration of 100 µg mL−1. The phytosynthesized Ag-NPs demonstrated a marked antimicrobial activity and also exhibited a potent cytotoxic effect against mouse melanoma F10B16 cells. The key findings of this study indicate that synthesized Ag-NPs exhibit profound therapeutic activity and could be potentially ideal alternatives in medicinal applications.

Experimental study on mechanical properties of polypropylene nanocomposites reinforced with a hybrid graphene/PP-g-MA/kenaf fiber by response surface methodology

2021 ◽  
pp. 009524432110153
Author(s):  
Jaber Mirzaei ◽  
Abdolhossein Fereidoon ◽  
Ahmad Ghasemi-Ghalebahman
Keyword(s):  
Mechanical Properties ◽  
Response Surface Methodology ◽  
Elastic Modulus ◽  
Response Surface ◽  
Graphene Nanosheets ◽  
Hot Press ◽  
Kenaf Fiber ◽  
Polypropylene Nanocomposites ◽  
Kenaf Fibers ◽  
Internal Mixer

In this study, the mechanical properties of polypropylene (PP)-based nanocomposites reinforced with graphene nanosheets, kenaf fiber, and polypropylene-grafted maleic anhydride (PP-g-MA) were investigated. Response surface methodology (RSM) based on Box–Behnken design (BBD) was used as the experimental design. The blends fabricated in three levels of parameters include 0, 0.75, and 1.5 wt% graphene nanosheets, 0, 7.5, and 15 wt% kenaf fiber, and 0, 3, and 6 wt% PP-g-MA, prepared by an internal mixer and a hot press machine. The fiber length was 5 mm and was being constant for all samples. Tensile, flexural, and impact tests were conducted to determine the blend properties. The purpose of this research is to achieve the highest mechanical properties of the considered nanocomposite blend. The addition of graphene nanosheets to 1 wt% increased the tensile, flexural, and impact strengths by 16%, 24%, and 19%, respectively, and an addition up to 1.5 wt% reduced them. With further addition of graphene nanosheets until 1.5 wt%, the elastic modulus was increased by 70%. Adding the kenaf fiber up to 15 wt% increased the elastic modulus, tensile, flexural, and impact strength by 24%, 84%, 18%, and 11%, respectively. The addition of PP-g-MA has increased the adhesion, dispersion and compatibility of graphene nanosheets and kenaf fibers with matrix. With 6 wt% PP-g-MA, the tensile strength and elastic modulus were increased by 18% and 75%, respectively. The addition of PP-g-MA to 5 wt% increased the flexural and impact strengths by 10% and 5%, respectively. From the entire experimental data, the optimum values for elastic modulus, as well as, tensile, flexural, and impact strengths in the blends were obtained to be 4 GPa, 33.7896 MPa, 57.6306 MPa, and 100.1421 J/m, respectively. Finally, samples were studied by FE-SEM to check the dispersion of graphene nanosheets, PP-g-MA and kenaf fibers in the polymeric matrix.

scholarly journals Controlling the Kinetics of an Enzymatic Reaction through Enzyme or Substrate Confinement into Lipid Mesophases with Tunable Structural Parameters

2020 ◽  
Vol 21 (14) ◽  
pp. 5116
Author(s):  
Marco Mendozza ◽  
Arianna Balestri ◽  
Costanza Montis ◽  
Debora Berti
Keyword(s):  
Reaction Kinetics ◽  
Self Assembly ◽  
Liquid Crystalline ◽  
Structural Parameters ◽  
Enzymatic Reaction ◽  
X Ray Scattering ◽  
Nitrophenyl Phosphate ◽  
Vis Spectroscopy ◽  
Kinetics Of ◽  
Enzyme Alkaline Phosphatase

Lipid liquid crystalline mesophases, resulting from the self-assembly of polymorphic lipids in water, have been widely explored as biocompatible drug delivery systems. In this respect, non-lamellar structures are particularly attractive: they are characterized by complex 3D architectures, with the coexistence of hydrophobic and hydrophilic regions that can conveniently host drugs of different polarities. The fine tunability of the structural parameters is nontrivial, but of paramount relevance, in order to control the diffusive properties of encapsulated active principles and, ultimately, their pharmacokinetics and release. In this work, we investigate the reaction kinetics of p-nitrophenyl phosphate conversion into p-nitrophenol, catalysed by the enzyme Alkaline Phosphatase, upon alternative confinement of the substrate and of the enzyme into liquid crystalline mesophases of phytantriol/H2O containing variable amounts of an additive, sucrose stearate, able to swell the mesophase. A structural investigation through Small-Angle X-ray Scattering, revealed the possibility to finely control the structure/size of the mesophases with the amount of the included additive. A UV–vis spectroscopy study highlighted that the enzymatic reaction kinetics could be controlled by tuning the structural parameters of the mesophase, opening new perspectives for the exploitation of non-lamellar mesophases for confinement and controlled release of therapeutics.

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