scholarly journals Fire and Gas Barrier Properties of Poly(styrene-co-acrylonitrile) Nanocomposites Using Polycaprolactone/Clay Nanohybrid Based-Masterbatch

2008 ◽  
Vol 2008 ◽  
pp. 1-11 ◽  
Author(s):  
S. Benali ◽  
A. Olivier ◽  
P. Brocorens ◽  
L. Bonnaud ◽  
M. Alexandre ◽  
...  
Keyword(s):  
Barrier Properties ◽  
Hydroxyl Groups ◽  
Gas Barrier ◽  
Clay Dispersion ◽  
Force Microscopy ◽  
Atomic Force ◽  
The Matrix ◽  
Inorganic Content ◽  
Barrier Resistance ◽  
Silicate Layers

Exfoliated nanocomposites are prepared by dispersion of poly(ε-caprolactone) (PCL) grafted montmorillonite nanohybrids used as masterbatches in poly(styrene-co-acrylonitrile) (SAN). The PCL-grafted clay nanohybrids with high inorganic content are synthesized by in situ intercalative ring-opening polymerization ofε-caprolactone between silicate layers organomodified by alkylammonium cations bearing two hydroxyl functions. The polymerization is initiated by tin alcoholate species derived from the exchange reaction of tin(II) bis(2-ethylhexanoate) with the hydroxyl groups borne by the ammonium cations that organomodified the clay. These highly filled PCL nanocomposites (25 wt% in inorganics) are dispersed as masterbatches in commercial poly(styrene-co-acrylonitrile) by melt blending. SAN-based nanocomposites containing 3 wt% of inorganics are accordingly prepared. The direct blend of SAN/organomodified clay is also prepared for sake of comparison. The clay dispersion is characterized by wide-angle X-ray diffraction (WAXD), atomic force microscopy (AFM), and solid state NMR spectroscopy measurements. The thermal properties are studied by thermogravimetric analysis. The flame retardancy and gas barrier resistance properties of nanocomposites are discussed both as a function of the clay dispersion and of the matrix/clay interaction.

scholarly journals An Insight into Amorphous Shear Band in Magnetorheological Solid by Atomic Force Microscope

Materials ◽  
2021 ◽  
Vol 14 (16) ◽  
pp. 4384
Author(s):  
Mohd Aidy Faizal Johari ◽  
Asmawan Mohd Sarman ◽  
Saiful Amri Mazlan ◽  
Ubaidillah U ◽  
Nur Azmah Nordin ◽  
...  
Keyword(s):  
Stress Relaxation ◽  
Shear Band ◽  
Shear Bands ◽  
Test Duration ◽  
Phase Imaging ◽  
Force Microscopy ◽  
Atomic Force ◽  
The Matrix ◽  
Relaxation Stress ◽  
Band Deformation

Micro mechanism consideration is critical for gaining a thorough understanding of amorphous shear band behavior in magnetorheological (MR) solids, particularly those with viscoelastic matrices. Heretofore, the characteristics of shear bands in terms of formation, physical evolution, and response to stress distribution at the localized region have gone largely unnoticed and unexplored. Notwithstanding these limitations, atomic force microscopy (AFM) has been used to explore the nature of shear band deformation in MR materials during stress relaxation. Stress relaxation at a constant low strain of 0.01% and an oscillatory shear of defined test duration played a major role in the creation of the shear band. In this analysis, the localized area of the study defined shear bands as varying in size and dominantly deformed in the matrix with no evidence of inhibition by embedded carbonyl iron particles (CIPs). The association between the shear band and the adjacent zone was further studied using in-phase imaging of AFM tapping mode and demonstrated the presence of localized affected zone around the shear band. Taken together, the results provide important insights into the proposed shear band deformation zone (SBDZ). This study sheds a contemporary light on the contentious issue of amorphous shear band deformation behavior and makes several contributions to the current literature.

Ball-Milling Graphite Used for Synthesis of Biocompatible Blue Luminescent Graphene Quantum Dots

2021 ◽  
Vol 6 (2) ◽  
Author(s):  
Zhou J ◽  
◽  
Dong Y ◽  
Ma Y ◽  
Zhang T ◽  
...  
Keyword(s):  
Quantum Dots ◽  
Ball Milling ◽  
Graphene Quantum Dots ◽  
Raw Material ◽  
Hydroxyl Groups ◽  
High Quality ◽  
Widespread Application ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron

Graphene Quantum Dots (GQDs) have been prepared by oxidationhydrothermal reaction, using ball-milling graphite as the starting materials. The prepared GQDs are endowed with excellent luminescence properties, with the optimum emission of 320nm. Blue photoluminescent emitted from the GQDs under ultraviolet light. The GQDs are ~3nm in width and 0.5~2 nm in thickness, revealed by high-resolution transmission electron microscopy and atomic force microscopy. In addition, Fourier transform infrared spectrum evidences the existence of carbonyl and hydroxyl groups, meaning GQDs can be dispersed in water easily and used in cellar imaging, and blue area inside L929 cells were clearly observed under the fluorescence microscope. Both low price of raw material and simple prepared method contribute to the high quality GQDs widespread application in future.

scholarly journals Poly(furfuryl alcohol)-Polycaprolactone Blends

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1069 ◽  
Author(s):  
Gabriele Nanni ◽  
José A. Heredia-Guerrero ◽  
Uttam C. Paul ◽  
Silvia Dante ◽  
Gianvito Caputo ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Furfuryl Alcohol ◽  
Barrier Properties ◽  
Tensile Tests ◽  
Attenuated Total Reflection ◽  
Toxicity Tests ◽  
Scanning Calorimetry ◽  
Blend Films ◽  
Force Microscopy ◽  
Atomic Force

Poly(furfuryl alcohol) (PFA) is a bioresin synthesized from furfuryl alcohol (FA) that is derived from renewable saccharide-rich biomass. In this study, we compounded this bioresin with polycaprolactone (PCL) for the first time, introducing new functional polymer blends. Although PCL is biodegradable, its production relies on petroleum precursors such as cyclohexanone oils. With the method proposed herein, this dependence on petroleum-derived precursors/monomers is reduced by using PFA without significantly modifying some important properties of the PCL. Polymer blend films were produced by simple solvent casting. The blends were characterized in terms of surface topography by atomic force microscopy (AFM), chemical interactions between PCL and PFA by attenuated total reflection-Fourier transform infrared (ATR-FTIR), crystallinity by XRD, thermal properties by differential scanning calorimetry (DSC), and mechanical properties by tensile tests and biocompatibility by direct and indirect toxicity tests. PFA was found to improve the gas barrier properties of PCL without compromising its mechanical properties, and it demonstrated sustained antioxidant effect with excellent biocompatibility. Our results indicate that these new blends can be potentially used in diverse applications ranging from food packing to biomedical devices.

Structure and Properties of Hybrid Polyurethane Composites with Carboxyalumoxanes

2008 ◽  
Vol 587-588 ◽  
pp. 212-216 ◽  
Author(s):  
Magdalena Jurczyk-Kowalska ◽  
Joanna Ryszkowska
Keyword(s):  
In Situ Polymerization ◽  
Structure And Properties ◽  
Mechanical Mixing ◽  
Scanning Calorimetry ◽  
Force Microscopy ◽  
Atomic Force ◽  
The Matrix ◽  
Polyurethane Composites ◽  
Polyurethane Matrix

Carboxyalumoxanes have been incorporated into a polyurethane matrix by in situ polymerization. The filler was dispersed in the polyurethane matrix by either both ultrasonic and mechanical mixing or by mechanical mixing alone. The physico-mechanical properties of the composites have been characterized using scanning electron microscopy (SEM), atomic force microscopy (AFM), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Using ultrasound improves the degree of dispersion of the fillers in the matrix, but it also causes changes in the structure of the polyurethane matrix.

Hydrogen-Bonded Macrocluster Formation of 1-Propanol and 2-Propanol on Silica Surfaces

2003 ◽  
Vol 56 (10) ◽  
pp. 1071 ◽  
Author(s):  
Masashi Mizukami ◽  
Kazue Kurihara
Keyword(s):  
Hydrogen Bonding ◽  
Long Range ◽  
Hydroxyl Groups ◽  
Similar Amount ◽  
Colloidal Probe ◽  
Force Microscopy ◽  
Silica Surfaces ◽  
Atomic Force ◽  
Aggregation Structure ◽  
Hydrogen Bonded

We have investigated the adsorption of 1- and 2-propanol on silica surfaces from their mixtures with cyclohexane using a combination of colloidal probe atomic force microscopy, adsorption excess isotherms, and FTIR spectroscopy in the ATR mode. The adsorption isotherm indicated that a similar amount of each alcohol was adsorbed on the silica surfaces. FTIR spectra revealed that 1-propanol adsorbed on the surface employing hydrogen-bonding between the surface silanol groups and the hydroxyl groups of 1-propanol as well as between the hydroxyl groups of 1-propanol in the form of a linear zig-zag structure. This structure is similar to the linear hydrogen-bonded structure of ethanol, which we have found on silica and called a ‘surface molecular macrocluster’ (M. Mizukami, M. Moteki, K. Kurihara, J. Am. Chem. Soc. 2002, 124, 12 889). The contact of adsorbed layers of 1-propanol on the opposed silica surfaces brought about the long-range attraction extending to 69 ± 9 nm at 0.1 mol-% 1-propanol. 2-Propanol was also adsorbed on the surface by the hydrogen-bonding, however, in the form of a cyclic structure. No long-range attraction was observed in the 2-propanol/cyclohexane binary liquids at 0.1–6.0 mol-%. The absence of a long-range attraction can be explained by the cyclic aggregation structure of 2-propanol on the surface.

A Novel Approach to the Functionalisation of Pristine Carbon Fibre Using Azomethine 1,3-Dipolar Cycloaddition

2015 ◽  
Vol 68 (2) ◽  
pp. 335 ◽  
Author(s):  
Linden Servinis ◽  
Thomas R. Gengenbach ◽  
Mickey G. Huson ◽  
Luke C. Henderson ◽  
Bronwyn L. Fox
Keyword(s):  
Carbon Fibre ◽  
Photoelectron Spectroscopy ◽  
Cycloaddition Reaction ◽  
Fibre Surface ◽  
Single Fibre ◽  
Dipolar Cycloaddition ◽  
Force Microscopy ◽  
Atomic Force ◽  
Novel Approach ◽  
The Matrix

We demonstrate the utilisation of an azomethine 1,3-dipolar cycloaddition reaction with carbon fibre to graft complex molecules onto the fibre surface. In an effort to enhance the interfacial interaction of the fibre to the matrix, the functionalised fibres possessed a pendant amine that is able to interact with epoxy resins. Functionalisation was supported by X-ray photoelectron spectroscopy and the grafting process had no detrimental effects on tensile strength compared with the control (untreated) fibres. Also, microscopic roughness (as determined by atomic force microscopy) and fibre topography were unchanged after the described treatment process. This methodology complements existing methodology aimed at enhancing the surface of carbon fibres for advanced material applications while not compromising the desirable strength profile. Single-fibre fragmentation tests show a statistically significant decrease in fragment length compared with the control fibres in addition to transverse cracking within the curing resin, both of which indicate an enhanced interaction between fibre and resin.

scholarly journals Blends of poly(butylene adipate-co-terephthalate) and thermoplastic whey protein isolate: a compatibilization study

2021 ◽  
Author(s):  
Marina Fernandes Cosate de Andrade ◽  
Hugo Campos Loureiro ◽  
Claire Isabel Grígoli de Luca Sarantopóulos ◽  
Ana Rita Morales
Keyword(s):  
Whey Protein ◽  
Complex Viscosity ◽  
Barrier Properties ◽  
Whey Protein Isolate ◽  
Mechanical Tests ◽  
Protein Isolate ◽  
Degree Of Crystallinity ◽  
Force Microscopy ◽  
Rate Region ◽  
The Matrix

Abstract This work assesses the influence of the plasticizer polyethylene glycol (PEG) on the compatibilization of poly(butylene adipate-co-terephthalate) (PBAT) and thermoplastic whey protein isolate (WPIT) blends. To prepare the blends, WPI was denatured at 90 oC, in the presence of PEG, to become a thermoplastic material. Dried WPIT was later mechanically blended with PBAT using a torque rheometer at 160 oC and 80 rpm. Two blends were prepared: 90% of PBAT/10% of WPIT (90_10) and 70% of PBAT/30% of WPIT (70_30). Scanning electron microscopy (SEM) analyses showed a homogenous blend morphology and good interaction between the dispersed phase and the matrix. Atomic force microscopy-based infrared spectroscopy (AFM-IR) showed PBAT and WPIT bands in all studied regions of both blends, which suggests that these materials presented partial miscibility. The viscosity ratio of the PBAT/WPIT system was less than 3.5 in the high shear rate region in complex viscosity curves, which indicates that droplet break-up of WPIT may occur by the drop fibrillation mechanism. The addition of WPIT reduced the degree of crystallinity of PBAT in the blends in comparison to pristine PBAT as shown by X-ray diffraction (XRD). Mechanical tests showed that blend tensile strength and elongation at break decreased with the addition of WPIT. Elastic modulus of the blends increased compared to pristine PBAT. Barrier properties were also evaluated showing that the oxygen permeability coefficient reduced by 20% for the blend with 30% of WPIT and vapor water permeability increased with the addition of WPIT.

scholarly journals Autoxidation Enhances Anti-Amyloid Potential of Flavone Derivatives

Antioxidants ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1428
Author(s):  
Andrius Sakalauskas ◽  
Mantas Ziaunys ◽  
Ruta Snieckute ◽  
Vytautas Smirnovas
Keyword(s):  
Amyloid Beta ◽  
Intensity Change ◽  
Hydroxyl Groups ◽  
Force Microscopy ◽  
Atomic Force ◽  
Tht Fluorescence ◽  
Spectrum Change ◽  
Amyloidogenic Protein ◽  
Before And After ◽  
Initial Molecule

The increasing prevalence of amyloid-related disorders, such as Alzheimer’s or Parkinson’s disease, raises the need for effective anti-amyloid drugs. It has been shown on numerous occasions that flavones, a group of naturally occurring anti-oxidants, can impact the aggregation process of several amyloidogenic proteins and peptides, including amyloid-beta. Due to flavone autoxidation at neutral pH, it is uncertain if the effective inhibitor is the initial molecule or a product of this reaction, as many anti-amyloid assays attempt to mimic physiological conditions. In this work, we examine the aggregation-inhibiting properties of flavones before and after they are oxidized. The oxidation of flavones was monitored by measuring the UV-vis absorbance spectrum change over time. The protein aggregation kinetics were followed by measuring the amyloidophilic dye thioflavin-T (ThT) fluorescence intensity change. Atomic force microscopy was employed to image the aggregates formed with the most prominent inhibitors. We demonstrate that flavones, which undergo autoxidation, have a far greater potency at inhibiting the aggregation of both the disease-related amyloid-beta, as well as a model amyloidogenic protein—insulin. Oxidized 6,2′,3′-trihydroxyflavone was the most potent inhibitor affecting both insulin (7-fold inhibition) and amyloid-beta (2-fold inhibition). We also show that this tendency to autoxidize is related to the positions of the flavone hydroxyl groups.

Damage Precursors in Individual Microfibers

2016 ◽  
Author(s):  
Daniel P. Cole ◽  
Todd C. Henry ◽  
Frank Gardea ◽  
Robert Haynes
Keyword(s):  
Early Stage ◽  
Force Microscopy ◽  
Atomic Force ◽  
Local Material ◽  
Before And After ◽  
The Matrix ◽  
Local Properties ◽  
Damage Precursor ◽  
The Individual ◽  
Multiscale Composites

Structural health monitoring of composite materials is limited by the lack of fundamental understanding of early stage damage at the local material level. This includes damage precursor formation on fiber surfaces, within the matrix, and at the fiber-matrix interface/interphase. In this effort, we present a micro-/nano-scale technique for characterizing damage precursor formation on individual carbon fibers exposed to cyclic tensile loads. Nanoindentation and atomic force microscopy (AFM) were used to study the local properties of the individual microfibers before and after global loading events. An AFM image analysis was used to track evolution of topography on the fiber surfaces. The work is a first step toward understanding damage precursor formation in individual microfibers; the work is expected to enable multiscale composites modeling efforts as well as enable the development of future self-sensing materials.

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