Nguyen Thuy Chinh

Effects of maleic anhydride grafted ethylene/vinyl acetate copolymer (EVA) on the properties of EVA/silica nanocomposites

AbstractTernary nanocomposites based on ethylene/vinyl acetate copolymer (EVA), maleic anhydride-grafted EVA (EVAgMA), and nanosilica were prepared in a Haake Rheomixer. The structure of the EVA/EVAgMA/silica nanocomposites was characterized by Fourier transform infrared spectroscopy and field emission scanning electron microscopy. The blending sequence was found to have a significant effect on the microstructure of EVA/EVAgMA/silica nanocomposites and the dispersion behavior of the nanosilica in the EVA matrix. The tensile properties (tensile strength and elongation at break), thermal behavior, crystalline structure and weatherability of the nanocomposites were also studied. The results showed that the above properties of the nanocomposites were enhanced remarkably using 1 wt% EVAgMA.

Tensile, rheological properties, thermal stability, and morphology of ethylene vinyl acetate copolymer/silica nanocomposites using EVA-g-maleic anhydride

In this article, we present a study on the properties of ethylene vinyl acetate copolymer/silica nanocomposites prepared in absence and presence of EVA-g-maleic anhydride as a compatibilizer between silica nanoparticles and ethylene vinyl acetate matrix. A series of ethylene vinyl acetate/silica nanocomposites with different contents of silica nanoparticles were prepared by solution method. EVA-g-maleic anhydride with 0.5 wt% maleic anhydride groups was added to all ethylene vinyl acetate/silica nanocomposites. Fourier transform infrared, field emission scanning electron microscopy, rheology behavior, and thermogravimetry analysis were used to characterize the structure, morphology, rheological, and thermal properties of the nanocomposites, respectively. The Fourier transform infrared spectra and field emission scanning electron microscopy micrographs showed that the hydroxyl groups on the surface of silica nanoparticles interact with maleic anhydride groups in EVA-g-maleic anhydride and lead to a finer dispersion of individual silica nanoparticles in the ethylene vinyl acetate matrix. The rheological properties and thermal stability of ethylene vinyl acetate/silica nanocomposites were significantly increased after adding EVA-g-maleic anhydride into the nanocomposites. Mechanical properties including tensile strength and elongation at break of the nanocomposites were mainly affected by the content of silica nanoparticles. For the tensile strength as well as elongation at break of the nanocomposites, a maximum value was observed at the content of 0.5 wt% of silica nanoparticles. The addition of EVA-g-maleic anhydride into ethylene vinyl acetate/silica nanocomposites resulted in a further improvement of mechanical properties of the nanocomposites.

Sustainable composite materials based on ethylene-vinylacetate copolymer and organo-modified silica

Abstract Silica nanoparticles (SNPs) were modified by different amounts of 3-aminopropyltriethoxysilane (APTES). Nanocomposites based on ethylene vinyl acetate copolymer (EVA) and modified SNP (m-SNP) were prepared by the melt mixing method. They were characterized by Haake torque measurement, differential scanning calorimetry (DSC), horizontal burning test, scanning electron microscopy. Accelerated weather testing of the nanocomposites was performed according to ASTM D4329 (cycle A) for 168 h. The Haake torque indicates that the relative melt viscosity of EVA/m-SNPs is slightly higher than that of EVA/SNP nanocomposites. The DSC and burning test results show that m-SNPs decrease crystallinity degree and flammability of EVA. After accelerated weather testing, the relative amount of C=O groups in EVA/m-SNP nanocomposites is lower than that in EVA/SNP nanocomposites. Micro crack of EVA/m-SNP nanocomposite is smaller than that of EVA/SNP nanocomposite. In our study, the EVA/m-SNP nanocomposites with good tensile properties, flame and weather resistance can be used as sustainable materials in some technique fields.

Tensile, Thermal, Dielectric and Morphological Properties of Polyoxymethylene/Silica Nanocomposites

This paper presents the tensile, thermal, dielectric and morphological properties of composites based on polyoxymethylene (POM) and nanosilica (NS) prepared by melt mixing method at 190 °C. Based on the torque readings, the processing of POM/NS composites were found to be easier in comparison to only POM. The FT-IR spectra analysis of the POM/NS nanocomposites showed the presence of peak at approximately 910 cm-1, attributed to the Si-O and C-O groups in NS and POM on the POM/NS nanocomposite. The absorption at these peaks increased on gradually increasing the content of NS. Tensile property testing (tensile strength, elongation at break, and Youngs modulus) indicated that the tensile strength of POM/NS nanocomposites increases as the NS content increases from 0.5 wt.% to 1.5 wt.%, and sharply dropped when the NS content was more than 2 wt.%. A similar trend was observed for Youngs modulus and elongation at break of the nanocomposites. The DSC analysis of the nanocomposites showed that the melting temperature (Tm) of POM/NC composites increased in the presence of low weight % of NS which can be attributed to the interaction between POM and NS leading to the rising crystallinity of all nanocomposites. POM/NS have a slightly higher temperature resistance as confirmed from the TGA analysis and POM/NS 1.5 wt.% had the maximum degradation temperature (Tmax) value and consequently the lowest weight loss. The dielectric constant of the nanocomposites increased from 3.26 to 3.56, while the dielectric loss tangent and volume resistivity were dropped, corresponding to the NS content from 0.5 to 2 wt.%. The SEM images of POM/NS nanocomposites demonstrated that the NS particles were dispersed relatively regularly into POM with a size in the range of 100 to 500 nm. They were dispersed more regularly into the polymer matrix at 1.5 wt.% NS. Based on the obtained results, the suitable NS content for the preparation of the POM/NS nanocomposites was found to be 1.5 wt.%.

Polylactic Acid/Chitosan Nanoparticles Loading Nifedipine: Characterization Findings and In Vivo Investigation in Animal

This paper presents the results of zeta potential, water contact angle, atomic force microscopy image, in vitro solubility, and content of heavy metals in polylactic acid (PLA)/chitosan (CS) nanoparticles loading nifedipine. In addition, the In Vivo test of the PLA/CS nanoparticles loading nifedipine in the mice is also one of highlights of this work. The Zeta potential result shows that the charged surface of the PLA/CS nanoparticles loading nifedipine is neutral, negative or complex depending on nifedipine content. Nifedipine plays a role in increase of hydrophobic property, swelling degree and regular surface as well as decrease of surface rough of the nanoparticles. The PLA/CS/nifedipine nanoparticles are dissolved in the solutions with pH 6.8, pH 4.5 and pH 1.2. The In Vivo test of PLA/CS nanoparticles loading nifedipine on mice was evaluated by the change in diastolic pressure, systolic pressure, arterial pressure and heart rate. The obtained results confirm that the PLA/CS nanoparticles loading nifedipine is suitable to apply in the treatment of hypertension patients lately.

Improvement of Mechanical and Dielectric Properties of Epoxy Resin Using CNTs/ZnO Nanocomposite

In this study, carbon nanotubes (CNTs)/ZnO composites had been prepared using the sol-gel method and then incorporated into an epoxy resin for reinforcement of mechanical and electrical properties. Fourier Transform Infrared (FTIR), X-ray diffraction (XRD) Field Emission Scanning Electron Microscope (FE-SEM) analyses show that the ZnO nanoparticles deposited on CNTs were crystallized in a hexagonal wurtzite structure. Average particle size of ZnO deposited on the CNT was about 8 nm. The mechanical and dielectric properties of epoxy containing CNTs/ZnO were investigated in comparison to epoxy resin and epoxy resin containing only CNT or ZnO nanoparticles. The results indicated that tensile strength and elongation at break of the nanocomposite were substantially improved with the presence of CNTs/ZnO at the equal volume. The DSC analysis associate with the dielectric results shows that the behavior of epoxy/CNTs/ZnO is identical to epoxy/ZnO composite, and the CNTs is essential to the distributed arrangement of ZnO in the epoxy resin.

Characteristics and Morphology of Nanosilica Modified with Isopropyl Tri(dioctyl Phosphate) Titanate Coupling Agent

In order to improve dispersiveness of nanosilica in polymer matrix, surface organo-modification of nanosilica is necessary. This work reveals silica nanoparticles modified by titanate coupling agent isopropyltri (dioctylphosphate) titanate (KR12) in toluene solvent. Effect of reaction temperature, reaction time and reactant ratio on grafting efficiency have been studied by Thermogravimetric Analysis (TGA). The obtained results exhibit the grafted percentage of titanate coupling agent KR-12 on the surface of nanosilica increased quickly from 4.97 to 13.11 wt.% as increasing the content of KR-12 from 5 to 15 wt.% and raise slower from 13.21 to 13.43 wt.% as content of KR-12 in the range of 30 to 45 wt.%, respectively. The KR-12 content and grafting reaction time affect significantly on the grafting efficiency while temperature of grafting reaction is negative to the grafting efficiency. The results of analysis related to Infrared Spectroscopy and Energy-Dispersive X-ray spectroscopy (EDS) displayed titanate coupling agent KR-12 have been covalently bonded to surface of the nanosilica. The Transmission Electron Microscopy (TEM) images and size distribution indicated that after organic modification, nanosilica particles had average size about 86 nm and the agglomeration of nanoparticles decreased significantly. The obtained results showed that surface treatment of nanosilica with titanate coupling agent KR-12 was successful.

Study on characteristics, properties, and morphology of poly(lactic acid)/chitosan/hydroquinine green nanoparticles

Abstract Poly(lactic acid)/chitosan (PLA/CS) green nanoparticles containing hydroquinine (Hq) were prepared by emulsion method. The content of Hq was 10–50 wt% compared with the weight total of PLA and CS. The characteristics of these nanoparticles were analyzed by Fourier transform infrared (FTIR), differential scanning calorimetry, field emission scanning electron microscopy (FESEM), and particle size analysis. The wavenumbers of C=O, C=N, OH, and CH3 groups in FTIR spectra of the PLA/CS/Hq (PCHq) nanoparticles shifted in comparision with neat PLA, CS, and Hq that proved the interaction between these components. The FESEM images and particle size analysis results showed that the basic particle size of PCHq nanoparticles ranged between 100 and 200 nm. The Hq released from PLA/CS nanoparticles in pH 2 and pH 7.4 solutions was determined by ultraviolet-visible method. The obtained results indicated that the linear regression coefficient of calibration equation of Hq in the above solutions approximates 1. The Hq release from the PCHq nanoparticles includes fast release for the eight first testing hours, and then, controlled slow release. The Hq released process was obeyed according to the Korsmeyer-Peppas kinetic model.

Study on change of color and some properties of high density polyethylene/organo-modified calcium carbonate composites exposed naturally at Dong Hoi-Quang Binh

This paper presents the study on the UV-Vis spectra, change of color and some properties of high density polyethylene/organo-modified calcium carbonate (HDPE/m-CaCO 3 ) composites exposed naturally in Dong Hoi district, Quang Binh province (Vietnam). From June 2014 to June 2016, the samples of HDPE/m-CaCO 3 composites were tested naturally on outdoor shelves at Dong Hoi sea atmosphere region (at Dong Hoi, Quang Binh). The change of UV-VIS spectra, color and some properties of the HDPE/m-CaCO 3 composites depend on geographic, weather and climatic factors (solar radiation, temperature, humidity, etc.). In the UV-VIS spectra, the band at 265 nm showed the formation of the carbonyl groups such as ketone, lactone carbonyl and aliphatic ester which were occurred in photo-degradation process of HDPE/m-CaCO 3 composites. The results of color change indicated the surface of the samples of HDPE/m-CaCO 3 composites was lightened continuously with increasing natural exposure time and increased in total color difference value and significant loss in both redness and yellowness. Da*, Db* values and electrical breakdown of HDPE/m-CaCO 3 composites were decreased while their Dl*, DE, dielectric constant and dielectric loss were increased with rising natural exposure time. Dielectric constant of HDPE/m-CaCO 3 composites was in the range of 1.75 to 2.1 and dielectric loss of HDPE/m-CaCO 3 composites went up from 1.7 to 3.2 for 0 to 24 months. The electrical breakdown of HDPE/m-CaCO 3 composites reduced due to the decrease in the relative crystalline degree of the samples caused by the scission photo-degradation of HDPE macromolecules in HDPE/m-CaCO 3 composites for natural exposure time. Keywords. HDPE/CaCO 3 composites, photo-degradation, natural exposure, color change, electric properties, UV-Vis spectroscopy.

Tensile, electrical properties and morphology of polyethylene/modified fly ash composites using ultraflow

This paper presents relative melt viscosity, tensile, electrical properties and morphology of high density polyethylene (HDPE)/organo-modified fly ash (MFA) and HDPE/MFA/ultraflow (UTF) composites which were prepared by melt mixing method. Relative melt viscosity of HDPE was decreased with adding MFA and UTF into HDPE. Tensile properties (tensile strength, elongation at break and Young’s modulus) of HDPE/MFA/UTF composites were increased with rising UTF content to 5 wt.% and thereafter, they were dropped with the UTF content more than 5 wt.%. Electric properties (dielectric constant, dielectric loss and volume resistivity) of the HDPE/MFA and HDPE/MFA/UTF composites were investigated. The obtained parameters showed that the HDPE/MFA composites have electric insulation higher than HDPE/MFA/UTF composites. Morphology of the composite materials with and without using UTF was also studied by Field Emission Scanning Electron Microscopy (FESEM) images. The results indicated that the MFA was dispersed more regularly and less agglomerated in HDPE matrix with adding UTF into the HDPE/MFA composites.