Preparation and Characterization of Oligopeptide/M-Pluronic F127 Composite Membranes

2020 ◽  
Vol 996 ◽  
pp. 59-63
Author(s):  
Chuan Jun Xia ◽  
Ping Deng Ming ◽  
Ya Song Hu ◽  
Cong Cong Zhan ◽  
An Duo Zhou ◽  
...  
Keyword(s):  
Self Assembly ◽  
Structural Parameters ◽  
Composite Films ◽  
Composite Membranes ◽  
Intermolecular Forces ◽  
Pluronic F127 ◽  
Scanning Calorimetry ◽  
Dsc Measurements ◽  
Assembly Behavior

In the present study, oligopeptide (TEA) and modified Pluronic F127 (M-Pluronic F127) with different mass fraction composited by intermolecular forces. And the oligopeptide/M-Pluronic F127 composite membranes were prepared and investigated. The structural parameters of the membranes were characterized by fourier transform-infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) measurements. It was found that there had strong interaction between TEA and M-Pluronic F127 and the composite films with different proportions had different surface morphology and thermal stability. The characteristics of the membranes were related to the significant changes of the self-assembly behavior of the TEA modified by M-Pluronic F127.

Enhancing the Thermal and Mechanical Characteristics of Polyvinyl Alcohol (PVA)-Hemp Protein Particles (HPP) Composites

2021 ◽  
Vol 36 (2) ◽  
pp. 137-143
Author(s):  
S. A. Awad
Keyword(s):  
Mechanical Properties ◽  
Elevated Temperatures ◽  
Composite Films ◽  
Tensile Tests ◽  
Mechanical Analysis ◽  
Decomposition Temperature ◽  
Scanning Calorimetry ◽  
Solution Casting Method ◽  
Protein Particles

Abstract This paper aims to describe the thermal, mechanical, and surface properties of a PVA/HPP blend whereby the film was prepared using a solution casting method. The improvements in thermal and mechanical properties of HPP-based PVA composites were investigated. The characterization of pure PVA and PVA composite films included tensile tests, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results of TGA and DSC indicated that the addition of HPP increased the thermal decomposition temperature of the composites. Mechanical properties are significantly improved in PVA/HPP composites. The thermal stability of the PVA composite increased with the increase of HPP filler content. The tensile strength increased from 15.74 ± 0.72 MPa to 27.54 ± 0.45 MPa and the Young’s modulus increased from 282.51 ± 20.56 MPa to 988.69 ± 42.64 MPa for the 12 wt% HPP doped sample. Dynamic mechanical analysis (DMA) revealed that at elevated temperatures, enhanced mechanical properties because of the presence of HPP was even more noticeable. Morphological observations displayed no signs of agglomeration of HPP fillers even in composites with high HPP loading.

scholarly journals A Facile Synthesis and Characterization of Highly Crystalline Submicro-Sized BiFeO3

Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 3035
Author(s):  
Dovydas Karoblis ◽  
Diana Griesiute ◽  
Kestutis Mazeika ◽  
Dalis Baltrunas ◽  
Dmitry V. Karpinsky ◽  
...  
Keyword(s):  
Bismuth Ferrite ◽  
Cost Effective ◽  
Xrd Analysis ◽  
Synthetic Approach ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Dsc Measurements ◽  
Optimal Annealing Temperature ◽  
Synthesized Materials

In this study, a highly crystalline bismuth ferrite (BFO) powder was synthesized using a novel, very simple, and cost-effective synthetic approach. It was demonstrated that the optimal annealing temperature for the preparation of highly-pure BFO is 650 °C. At lower or higher temperatures, the formation of neighboring crystal phases was observed. The thermal behavior of BFO precursor gel was investigated by thermogravimetric and differential scanning calorimetry (TG-DSC) measurements. X-ray diffraction (XRD) analysis and Mössbauer spectroscopy were employed for the investigation of structural properties. Scanning electron microscopy (SEM) was used to evaluate morphological features of the synthesized materials. The obtained powders were also characterized by magnetization measurements, which showed antiferromagnetic behavior of BFO powders.

scholarly journals Luminescence of SiO2-BaF2:Tb3+, Eu3+ Nano-Glass-Ceramics Made from Sol–Gel Method at Low Temperature

Nanomaterials ◽  
2022 ◽  
Vol 12 (2) ◽  
pp. 259
Author(s):  
Natalia Pawlik ◽  
Barbara Szpikowska-Sroka ◽  
Tomasz Goryczka ◽  
Ewa Pietrasik ◽  
Wojciech A. Pisarski
Keyword(s):  
Sol Gel ◽  
Three Dimensional ◽  
Glass Ceramics ◽  
Emission Spectra ◽  
Scanning Calorimetry ◽  
Light Emitting ◽  
Co Doping ◽  
Dsc Measurements ◽  
Decay Times

The synthesis and characterization of multicolor light-emitting nanomaterials based on rare earths (RE3+) are of great importance due to their possible use in optoelectronic devices, such as LEDs or displays. In the present work, oxyfluoride glass-ceramics containing BaF2 nanocrystals co-doped with Tb3+, Eu3+ ions were fabricated from amorphous xerogels at 350 °C. The analysis of the thermal behavior of fabricated xerogels was performed using TG/DSC measurements (thermogravimetry (TG), differential scanning calorimetry (DSC)). The crystallization of BaF2 phase at the nanoscale was confirmed by X-ray diffraction (XRD) measurements and transmission electron microscopy (TEM), and the changes in silicate sol–gel host were determined by attenuated total reflectance infrared (ATR-IR) spectroscopy. The luminescent characterization of prepared sol–gel materials was carried out by excitation and emission spectra along with decay analysis from the 5D4 level of Tb3+. As a result, the visible light according to the electronic transitions of Tb3+ (5D4 → 7FJ (J = 6–3)) and Eu3+ (5D0 → 7FJ (J = 0–4)) was recorded. It was also observed that co-doping with Eu3+ caused the shortening in decay times of the 5D4 state from 1.11 ms to 0.88 ms (for xerogels) and from 6.56 ms to 4.06 ms (for glass-ceramics). Thus, based on lifetime values, the Tb3+/Eu3+ energy transfer (ET) efficiencies were estimated to be almost 21% for xerogels and 38% for nano-glass-ceramics. Therefore, such materials could be successfully predisposed for laser technologies, spectral converters, and three-dimensional displays.

scholarly journals On the Aqueous Solution Behavior of C-Substituted 3,1,2-Ruthenadicarbadodecaboranes

Inorganics ◽  
2019 ◽  
Vol 7 (7) ◽  
pp. 91 ◽  
Author(s):  
Marta Gozzi ◽  
Benedikt Schwarze ◽  
Peter Coburger ◽  
Evamarie Hey-Hawkins
Keyword(s):  
Aqueous Solution ◽  
Aqueous Solutions ◽  
Self Assembly ◽  
Self Assembling ◽  
Vis Spectroscopy ◽  
Assembly Behavior ◽  
Biological Performance ◽  
Type 3

3,1,2-Ruthenadicarbadodecaborane complexes bearing the [C2B9H11]2− (dicarbollide) ligand are robust scaffolds, with exceptional thermal and chemical stability. Our previous work has shown that these complexes possess promising anti-tumor activities in vitro, and tend to form aggregates (or self-assemblies) in aqueous solutions. Here, we report on the synthesis and characterization of four ruthenium(II) complexes of the type [3-(η6-arene)-1,2-R2-3,1,2-RuC2B9H9], bearing either non-polar (R = Me (2–4)) or polar (R = CO2Me (7)) substituents at the cluster carbon atoms. The behavior in aqueous solution of complexes 2, 7 and the parent unsubstituted [3-(η6-p-cymene)-3,1,2-RuC2B9H11] (8) was investigated via UV-Vis spectroscopy, mass spectrometry and nanoparticle tracking analysis (NTA). All complexes showed spontaneous formation of self-assemblies (108–109 particles mL−1), at low micromolar concentration, with high polydispersity. For perspective applications in medicine, there is thus a strong need for further characterization of the spontaneous self-assembly behavior in aqueous solutions for the class of neutral metallacarboranes, with the ultimate scope of finding the optimal conditions for exploiting this self-assembling behavior for improved biological performance.

Preparation and Characterization of Blended Composite Membranes

2012 ◽  
Vol 488-489 ◽  
pp. 506-510 ◽  
Author(s):  
Sikander Rafiq ◽  
Zakaria Man ◽  
Abdulhalim Maulud ◽  
Nawshad Muhammad ◽  
Saikat Maitra
Keyword(s):  
Spectroscopic Analysis ◽  
Sol Gel ◽  
Composite Membranes ◽  
Hybrid Membranes ◽  
Ftir Analysis ◽  
Dsc Analysis ◽  
Scanning Calorimetry ◽  
Thermal Stability Of ◽  
Scanning Electron

Composite membranes were prepared by incorporating inorganic silica nanoparticles into blends of polysulfone/polyimide (PSF/PI) membranes via sol-gel route. Morphological structures of the developed membranes were carried out by scanning electron microscopy (SEM). Spectroscopic analysis of the hybrid membranes were done by fourier transform infrared spectroscopy (FTIR) analysis. Differential scanning calorimetry (DSC) analysis shows that the glass transition temperature (Tg) increased from 209oC to 238oC in the hybrid membranes followed by thermogravimetric analysis (TGA) that showed significant improvement in thermal stability of the developed membranes.

scholarly journals Preparation of Multicomponent Biocomposites and Characterization of Their Physicochemical and Mechanical Properties

2020 ◽  
Vol 4 (1) ◽  
pp. 18
Author(s):  
Yuriy A. Anisimov ◽  
Duncan E. Cree ◽  
Lee D. Wilson
Keyword(s):  
Mechanical Properties ◽  
Electrical Conductivity ◽  
Physicochemical Properties ◽  
In Situ Polymerization ◽  
Structural Parameters ◽  
Dye Adsorption ◽  
Mechanical Analysis ◽  
Scanning Calorimetry ◽  
Swelling Properties

This work focused on a mutual comparison and characterization of the physicochemical properties of three-component polymer composites. Binary polyaniline–chitosan (PANI–CHT) composites were synthesized by in situ polymerization of PANI onto CHT. Ternary composites were prepared by blending with a third component, polyvinyl alcohol (PVA). Composites with variable PANI:CHT (25:75, 50:50 and 75:25) weight ratios were prepared whilst fixing the composition of PVA. The structure and physicochemical properties of the composites were evaluated using thermal analysis (thermogravimetric analysis (TGA), differential scanning calorimetry (DSC)) and spectroscopic methods (infrared (IR), nuclear magnetic resonance (NMR)). The equilibrium and dynamic adsorption properties of composites were evaluated by solvent swelling in water, water vapour adsorption and dye adsorption isotherms. The electrical conductivity was estimated using current–voltage curves. The mechanical properties of the samples were evaluated using dynamic mechanical analysis (DMA) and correlated with the structural parameters of the composites. The adsorption and swelling properties paralleled the change in the electrical and mechanical properties of the materials. In most cases, samples with higher content of chitosan exhibit higher adsorption and mechanical properties, and lower conductivity. Acid-doped samples showed much higher adsorption, swelling, and electrical conductivity than their undoped analogues.

scholarly journals Morphology of crystalline–amorphous olefin block copolymers in solution characterized by small-angle neutron scattering and microscopy

2015 ◽  
Vol 48 (6) ◽  
pp. 1860-1869 ◽  
Author(s):  
Aurel Radulescu ◽  
Günter Goerigk ◽  
Lewis Fetters ◽  
Dieter Richter
Keyword(s):  
Block Copolymers ◽  
Neutron Scattering ◽  
Small Angle ◽  
Self Assembly ◽  
Small Angle Neutron Scattering ◽  
Chain Structure ◽  
Hierarchical Organization ◽  
Single Chain ◽  
Scanning Calorimetry ◽  
Assembly Behavior

The single-chain properties and self-assembly behavior in dilute solution of olefin block copolymers obtained by chain-shuttling technology and consisting of alternating crystallizable and amorphous ethylene/1-octene blocks were investigated by pinhole and focusing small-angle neutron scattering techniques, optical microscopy in bright-field and crossed-polarizer modes, and differential scanning calorimetry. The complex hydrocarbon soluble (precipitant free) macro-aggregates formed with decreasing temperature are characterized by spherulitic textures. The spherulites yield, on one hand, a morphology that depends on the chain structure properties and, on the other hand, multiple structural levels with a hierarchical organization that ranges from 10 Å up to tens of micrometres. This morphology displays peculiarities dictated by the polydisperse character of these materials.

scholarly journals Development and Characterization of Novel Active Chitosan Films Containing Fennel and Peppermint Essential Oils

Coatings ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 936 ◽  
Author(s):  
Ting Liu ◽  
Jingfan Wang ◽  
Fumin Chi ◽  
Zhankun Tan ◽  
Liu Liu
Keyword(s):  
Essential Oil ◽  
Composite Films ◽  
Environmental Scanning Electron Microscopy ◽  
Chitosan Film ◽  
Environmental Scanning ◽  
The Novel ◽  
Scanning Calorimetry ◽  
Chitosan Films ◽  
Water Swelling

The effects of fennel essential oil (FEO) and peppermint essential oil (PEO) on chitosan-based films were evaluated in this study. The results showed that the addition of FEO and PEO slightly increased the density and thickness, while significantly decreasing the moisture content, water swelling, and solubility properties. The color values (L, a, b, ΔE and whiteness index (WI)) of the composite films containing FEO and PEO changed obviously with a tendency toward yellowness, which was beneficial in resisting food decomposition caused by ultraviolet light. The differential scanning calorimetry (DSC) and fourier-transform-infrared (FTIR) results indicated that the addition of FEO and PEO affected the structure of the chitosan films, while the interaction between the chitosan and polyphenols in FEO and PEO established new hydrogen bonds and improved the thermal stability. The environmental scanning electron microscopy (ESEM) illustrated that the surfaces of the composite films containing FEO and PEO were smooth, but the cross-section was rougher than in pure chitosan film. Furthermore, the composite films containing FEO and PEO exhibited prominent antioxidant activity. In short, the novel active chitosan-based films with incorporated FEO and PEO present broad application prospects in fresh-cut meat or vegetable packaging.

Preparation and Characterization of Elastomers Based on Polydimethylsiloxane/Poly(methyl methacrylate) Blends

2012 ◽  
Vol 535-537 ◽  
pp. 1193-1196
Author(s):  
Nai Qiang Zhang ◽  
Jian Dong ◽  
Hong Yu Chen
Keyword(s):  
Methyl Methacrylate ◽  
Room Temperature ◽  
Radical Copolymerization ◽  
Cross Linking ◽  
Scanning Calorimetry ◽  
Silicone Elastomers ◽  
Poly Methyl Methacrylate ◽  
Dsc Measurements ◽  
Pmma Blends

Polydimethylsiloxane/poly (methyl methacrylate) (PDMS/PMMA) blends were prepared by radical copolymerization of methyl methacrylate (MMA) and divinylbenzene (DVB) in the presence of PDMS. Elastomers based on PDMS/PMMA blends were formed by cross-linking PDMS with methyltriethoxysilane (MTES). Mechanical property measurements show that the elastomers thus formed exhibit superior tensile strength with respect to general room temperature vulcanized silicone elastomers containing silica. Moreover, investigations were carried out on the elastomers by extraction, scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) measurements. SEM shows that the elastomer has a microphase-separated structure consisting of dispersed PMMA domains within a continuous PDMS matrix. DSC result shows that the elastomers display two glass transition temperatures and confirm the incompatible nature of PDMS and PMMA.

Preparation and Characterization of Dioxanone and Poly(dioxanone)

2013 ◽  
Vol 711 ◽  
pp. 22-25
Author(s):  
Kui Lin Deng ◽  
Wen Hui Jin ◽  
Fu Chen Zhang ◽  
Chun Xiu Li ◽  
Hui Juan Shen ◽  
...  
Keyword(s):  
Ring Opening ◽  
Raw Materials ◽  
Copper Chromite ◽  
Copper Nitrate ◽  
Ring Opening Polymerization ◽  
Scanning Calorimetry ◽  
H Nmr ◽  
Dsc Measurements ◽  
Ammonium Dichromate

In this paper, the ammonium dichromate and copper nitrate were used as raw materials to prepare the copper chromite, and nanocopper chromite as a catalyst was used to synthesize the monomer dioxanone in diethylene glycol dehydrogenation. Under the strict conditions of no water and no oxygen, the stannous octoate was selected to catalyze ring-opening polymerization of the dioxanone to prepare the polydioxanone. And dioxanone and its polymers were characterized with IR spectroscopy,1H NMR spectroscopy, thermogravimetric analysis (TG) and differential scanning calorimetry (DSC ) measurements.

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