Study Of Thermal And Mechanical Properties Of Clay/Polymer Nanocomposite Synthesized Via Modified Solution Blending

MRS Advances ◽  
2017 ◽  
Vol 2 (49) ◽  
pp. 2757-2762 ◽  
Author(s):  
Oscar Hernandez-Guerrero ◽  
Rubén Castillo-Pérez ◽  
Mireya Lizbeth Hernández-Vargas ◽  
Bernardo Fabián Campillo-Illanes
Keyword(s):  
Polymer Matrix ◽  
Polymer Nanocomposite ◽  
Hydrophobic Property ◽  
Scanning Calorimetry ◽  
Solution Blending ◽  
Nano Clay ◽  
Order Of Magnitude ◽  
Mixing Matrix ◽  
Mmt Clay ◽  
Matrix Concentration

ABSTRACTThe incorporation of layered nano-silicates in polymer matrix greatly enhances the properties of the polymer. At present, there are many applications of polymer nanocomposites including coatings and architectural, they are also parts of automotive and construction industry among others. The acrylics employed at the present study were based on butyl acrylate (BA), styrene (STY), and methacrylic acid (MAA), and the nano-clay was Na-montomorillonite (MMT). The MMT clay was added to the polymer, which is the mixing matrix in a physical state solution called blend. Furthermore, their mechanical, thermal and wettability of especially prepared acrylic montmorillonite (MMT) nanocomposites were performed. By increasing the MMT in the polymer matrix concentration the Young’s modulus tends to increase it by an order of magnitude. However, by Differential Scanning Calorimetry (DSC), the thermograms show an increase in the glass transition temperature of nanocomposites for all weight percentages of MMT. Also, the wetting angle was determined, in order to know how much water is retained on the surface of the nanocomposite; the results showed that by increasing the particle of nano clay in the polymer matrix will induce a hydrophobic property to the nanocomposite.

scholarly journals Role of Molecular Weight in Polymer Wrapping and Dispersion of MWNT in a PVDF Matrix

Polymers ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 162 ◽  
Author(s):  
Muthuraman Namasivayam ◽  
Mats R. Andersson ◽  
Joseph Shapter
Keyword(s):  
Molecular Weight ◽  
Electrical Properties ◽  
Polymer Matrix ◽  
Polymer Nanocomposite ◽  
Scanning Calorimetry ◽  
Crystallisation Behaviour ◽  
Effective Dispersion ◽  
Thermal And Electrical Properties ◽  
Polymer Wrapping

The thermal and electrical properties of a polymer nanocomposite are highly dependent on the dispersion of the CNT filler in the polymer matrix. Non-covalent functionalisation with a PVP polymer is an excellent driving force towards an effective dispersion of MWNTs in the polymer matrix. It is shown that the PVP molecular weight plays a key role in the non-covalent functionalisation of MWNT and its effect on the thermal and electrical properties of the polymer nanocomposite is reported herein. The dispersion and crystallisation behaviour of the composite are also evaluated by a combination of scanning electron microscopy (SEM) and differential scanning calorimetry (DSC).

scholarly journals A Characteristic Study of Polylactic Acid/Organic Modified Montmorillonite (PLA/OMMT) Nanocomposite Materials after Hydrolyzing

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 376
Author(s):  
Su-Mei Huang ◽  
Jiunn-Jer Hwang ◽  
Hsin-Jiant Liu ◽  
An-Miao Zheng
Keyword(s):  
Thermal Stability ◽  
Polylactic Acid ◽  
Decomposition Temperature ◽  
Material Strength ◽  
Scanning Calorimetry ◽  
Hydrolysis Process ◽  
Twin Screw ◽  
Thermal Pressing ◽  
Organophilic Clay ◽  
Mmt Clay

In this study, the montmorillonite (MMT) clay was modified with NH4Cl, and then the structures were exfoliated or intercalated in a polylactic acid (PLA) matrix by a torque rheometer in the ratio of 0.5, 3.0, 5.0 and 8.0 wt%. X-ray diffraction (XRD) revealed that the organic modified-MMT(OMMT) was distributed successfully in the PLA matrix. After thermal pressing, the thermal stability of the mixed composites was measured by a TGA. The mixed composites were also blended with OMMT by a co-rotating twin screw extruder palletizing system, and then injected for the ASTM-D638 standard specimen by an injection machine for measuring the material strength by MTS. The experimental results showed that the mixture of organophilic clay and PLA would enhance the thermal stability. In the PLA mixed with 3 wt% OMMT nanocomposite, the TGA maximum decomposition temperature (Tmax) rose from 336.84 °C to 339.08 °C. In the PLA mixed with 5 wt% OMMT nanocomposite, the loss of temperature rose from 325.14 °C to 326.48 °C. In addition, the elongation rate increased from 4.46% to 10.19% with the maximum loading of 58 MPa. After the vibrating hydrolysis process, the PLA/OMMT nanocomposite was degraded through the measurement of differential scanning calorimetry (DSC) and its Tg, Tc, and Tm1 declined.

scholarly journals The Correlation between Physical Crosslinking and Water-Soluble Drug Release from Chitosan-Based Microparticles

Pharmaceutics ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 455
Author(s):  
Emilia Szymańska ◽  
Katarzyna Woś-Latosi ◽  
Julia Jacyna ◽  
Magdalena Dąbrowska ◽  
Joanna Potaś ◽  
...  
Keyword(s):  
Drug Release ◽  
Polymer Matrix ◽  
Drug Loading ◽  
Water Soluble ◽  
Dissolution Behavior ◽  
Complex Nature ◽  
Prolonged Release ◽  
Scanning Calorimetry ◽  
Burst Effect ◽  
The Impact

Microparticles containing water-soluble zidovudine were prepared by spray-drying using chitosan glutamate and beta-glycerophosphate as an ion crosslinker (CF). The Box–Behnken design was applied to optimize the microparticles in terms of their drug loading and release behavior. Physicochemical studies were undertaken to support the results from dissolution tests and to evaluate the impact of the crosslinking ratio on the microparticles’ characteristics. The zidovudine dissolution behavior had a complex nature which comprised two phases: an initial burst effect followed with a prolonged release stage. The initial drug release, which can be modulated by the crosslinking degree, was primarily governed by the dissolution of the drug crystals located on the microparticles’ surfaces. In turn, the further dissolution stage was related to the drug diffusion from the swollen polymer matrix and was found to correlate with the drug loading. Differential Scanning Calorimetry (DSC) studies revealed the partial incorporation of a non-crystallized drug within the polymer matrix, which correlated with the amount of CF. Although CF influenced the swelling capacity of chitosan glutamate microparticles, surprisingly a higher amount of CF did not impact the time required for 80% of the drug to be released markedly. The formulation with the lowest polymer:CF ratio, 3:1, was selected as optimal, providing satisfactory drug loading and displaying a moderate burst effect within the first 30 min of the study, followed with a prolonged drug release of up to 210 min.

scholarly journals Melt-Cast Films Significantly Enhance Triamcinolone Acetonide Delivery to the Deeper Ocular Tissues

Pharmaceutics ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 158
Author(s):  
Akshaya Tatke ◽  
Narendar Dudhipala ◽  
Karthik Janga ◽  
Bhavik Soneta ◽  
Bharathi Avula ◽  
...  
Keyword(s):  
Triamcinolone Acetonide ◽  
Polymer Matrix ◽  
Rabbit Model ◽  
In Vivo Studies ◽  
Invasive Technique ◽  
Content Uniformity ◽  
Scanning Calorimetry ◽  
Ocular Tissues

Delivering an effective drug load to the posterior section of the ocular tissues, while using a non-invasive technique, has always been a challenge. In this regard, the goal of the present study was to develop sustained release triamcinolone acetonide (TA) loaded polymeric matrix films for ocular delivery. The TA-films were prepared in two different polymer matrices, with drug loadings of 10% and 20% w/w, and they were evaluated for ocular distribution in vivo in a conscious rabbit model. A 4% w/v TA suspension (TA-C) was used as a control for in vitro and in vivo studies. The TA-films, prepared with melt-cast technology, used polyethylene oxide (PEO) and Soluplus® as the polymer matrix. The films were evaluated with respect to assay, content uniformity, excipient interaction, and permeability across isolated rabbit sclera. The distribution of TA in the ocular tissues, post topical administration, was determined in New Zealand male albino rabbits as a function of dose, and was compared against TA-C. The assay of the 10% and 20% w/w film was in the range from 70–79% and 92–94% for the Soluplus® and PEO films, respectively, and content uniformity was in the range of 95–103% for both the films. The assay of the TA from Soluplus® films was less compared with the PEO films and showed an interaction with TA, as revealed by Differential Scanning Calorimetry (DSC). Hence, Soluplus® films were not selected for further studies. No interaction was observed between the drug and PEO polymer matrix. The enhancement of trans-scleral flux and permeability of TA was about 1.16 and 1.33-folds, respectively, from the 10% w/w PEO and 3.5 and 2.12-folds, respectively, from the 20% w/w PEO films, as compared with TA-C formulations. The in vivo studies demonstrate that significantly higher TA levels were observed in the anterior and posterior segments of the eye at the end of 6h with the PEO films. Therefore, the PEO based polymeric films were able to deliver TA into the back of the eye efficiently and for prolonged periods.

scholarly journals Polymer Nanocomposite Membranes

2018 ◽  
Vol 8 (7) ◽  
pp. 1181 ◽  
Author(s):  
Svetlana Kononova ◽  
Galina Gubanova ◽  
Eleonora Korytkova ◽  
Denis Sapegin ◽  
Katerina Setnickova ◽  
...  
Keyword(s):  
Thermal Properties ◽  
Polymer Matrix ◽  
Scientific Literature ◽  
Morphological Characteristics ◽  
Polymer Nanocomposite ◽  
Nanocomposite Materials ◽  
Sorption Mechanism ◽  
Nanocomposite Membranes ◽  
Nanocomposite Structure ◽  
Transport Channels

Based on the results of research works reflected in the scientific literature, the main examples, methods and approaches to the development of polymer inorganic nanocomposite materials for target membranes are considered. The focus is on membranes for critical technologies with improved mechanical, thermal properties that have the necessary capabilities to solve the problems of a selective pervaporation. For the purpose of directional changes in the parameters of membranes, effects on their properties of the type, amount and conditions of nanoparticle incorporation into the polymer matrix were analyzed. An influence of nanoparticles on the structural and morphological characteristics of the nanocomposite film is considered, as well as possibilities of forming transport channels for separated liquids are analyzed. Particular attention is paid to a correlation of nanocomposite structure-transport properties of membranes, whose separation characteristics are usually considered within the framework of the diffusion-sorption mechanism.

Enhanced dielectric performance and energy storage density of polymer/graphene nanocomposites prepared by dual fabrication

2018 ◽  
Vol 33 (2) ◽  
pp. 270-285 ◽  
Author(s):  
UO Uyor ◽  
API Popoola ◽  
OM Popoola ◽  
VS Aigbodion
Keyword(s):  
Energy Storage ◽  
Polymer Matrix ◽  
Vinylidene Fluoride ◽  
Energy Storage Materials ◽  
Energy Storage Density ◽  
Melt Mixing ◽  
Graphene Nanocomposites ◽  
Storage Density ◽  
Solution Blending ◽  
Dielectric Performance

Polymer/graphene nanocomposites (PGNs) have shown great potential as dielectric and energy storage materials. However, insolubility of graphene in most solvents, hydrophobic behaviour and poor dispersion in polymer matrix restrict wider fabrications and applications of PGNs. In this study, we present co-fabricated PGNs engineered by solution blending and melt compounding methods with improved dielectric performance. Further processing of PGNs by melt mixing after solution blending not only improved dispersion of graphene in the matrix but also ensured good interfacial interaction of the composites’ constituents and reduction of oxygen content in PGNs. Graphene nanoplatelets used in this study was slightly functionalized (fGNPs) to enhance dispersion in the polymer matrix. It was later characterized using Fourier transform infrared (FTIR) and Raman spectrometer. Scanning electron microscope (SEM) was used in morphological study of the fabricated composites. Dielectric properties, electrical conductivity, breakdown strength and energy storage capacity of the fabricated composites were investigated. The results obtained showed well-dispersed fGNPs in poly (vinylidene fluoride) (PVDF) matrix and improved dielectric performance. For instance, with 3.34 wt% and 6.67 wt% fGNPs co-fabricated composites, dielectric constant increased from about 9 for neat PVDF to 9930 and 38,418 at 100 Hz, respectively. While 7588 and 12,046 were respectively measured for solution blended-only composites at similar fGNPs content. These resulted to about 176.9% and 376.4% increase in energy storage density with 3.34 wt% and 6.67 wt% fGNPs co-fabricated composites when compared to their counterparts. These results were also credited to strong bonding, reduction of oxygen and recovered graphene structure by melt-mixing approach.

Recent Advances in Polymer-Based Nanocomposites: A Brief Review

2021 ◽  
Vol 13 ◽  
Author(s):  
S. K. Parida
Keyword(s):  
Electrical Properties ◽  
Polymer Nanocomposites ◽  
Polymer Matrix ◽  
Polymer Nanocomposite ◽  
Review Article ◽  
Nanosized Particles ◽  
Mechanical And Electrical Properties ◽  
Potential Applications ◽  
Manufacturing Techniques ◽  
Host Polymer

: This presented review article is constructed to be an extensive source for polymer nanocomposite researchers covering the relation of structure with property, manufacturing techniques, and potential applications when a small number of nanosized particles are added to a host polymer matrix. The exceptional structural, mechanical, and electrical properties of polymer nanocomposites after the addition of inorganic solid nanoparticles are elucidated by the large surface area of doped nanoparticles that interact with host polymer matrices. Due to the generation of ideas, the conventional methods of preparation of polymer nanocomposites are made more interesting. Hence, this brief review presents a sketch of different synthesis techniques, characterization, applications, and safety concerns for polymer nanocomposites.

Halogenated methacrylate-based aluminum oxide (Al2O3) nanocomposites

2015 ◽  
Vol 30 (6) ◽  
pp. 762-772
Author(s):  
Kathikar Abdul Wasi ◽  
Sakvai Mohammed Safiullah ◽  
Kottur Anver Basha
Keyword(s):  
Aluminum Oxide ◽  
Polymer Matrix ◽  
Glycidyl Methacrylate ◽  
Morphological Changes ◽  
Thermal Studies ◽  
Gel Permeation Chromatography ◽  
Decomposition Temperature ◽  
Scanning Calorimetry ◽  
Initial Decomposition Temperature ◽  
Mixing Techniques

The aim of the work is to prepare the halogenated methacrylate-based polymer nano-aluminum oxide (Al2O3) composites and to study the effect of incorporated nano-Al2O3 on morphological and thermal studies. A functional 2,4,6-tribromophenyl methacrylate- co-glycidyl methacrylate copolymer microspheres (poly(TBPMA- co-GMA); pTG) by emulsion solvent evaporation techniques, whereas (2,4,6-tribromophenyl methacrylate- co-glycidyl methacrylate)-Al2O3 nanocomposites (pTG-Al2O3 nanocomposites) were prepared by solution mixing techniques. The pTG and its Al2O3 nanocomposites were structurally characterized by Fourier transform infrared (FTIR) spectroscopy. Thermal studies of pTG and its Al2O3 nanocomposites were carried out by thermogravimetric analysis and differential scanning calorimetry . The molecular weight of the pTG was determined by gel permeation chromatography. The size distribution and morphology of the pTG and its Al2O3 nanocomposites were determined by scanning electron microscopy (SEM). The FTIR results reveal that there is no significant interaction between the polymer matrix and Al2O3 nanoparticle. The significant increase in the initial decomposition temperature and glass transition temperature of pTG-Al2O3 nanocomposites compared to its polymer was due to the incorporation of nano-Al2O3 in the polymer matrix. The SEM observation provides the information about the morphological changes that arise in polymer matrix due to the incorporation of nano-Al2O3.

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