Preparation and Characterization of GNP/TPU Composites

2014 ◽  
Vol 644-650 ◽  
pp. 4760-4762 ◽  
Author(s):  
Bao Feng Xu ◽  
Sheng Lai ◽  
Zhi Dan Lin ◽  
Jiang Ming Chen ◽  
Jun Lin
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Thermoplastic Polyurethane ◽  
Graphene Nanoplatelets ◽  
Melt Blending ◽  
Frictional Properties ◽  
Blending Method ◽  
Properties Of Composites

Graphene nanoplatelets (GNP) and thermoplastic polyurethane (TPU) have been often used as filler and matrix, respectively, to produce composites. In this work, TPU/GNP composites were prepared via a melt blending method. The mechanical properties and frictional properties of TPU/GNP composites were investigated. Because the GNP is very expensive, we investigated to use graphite as the filler, to use PP-g-MAH as the compatibilizer and examined the characteristics of the prepared composites. Frictional properties and mechanical properties of GNP/TPU composites remarkably improve when adding PP-g-MAH as the compatibilizer. Tensile strength of composite containing 10wt % of GNP and 10wt% PP-g-MAH was measured as 25.5MPa. When the graphite was used to replace for GNP, the frictional properties of composites decreased, but the mechanical properties improved.

Preparation and Characterization of GNP/Nylon Composites

2014 ◽  
Vol 556-562 ◽  
pp. 339-342 ◽  
Author(s):  
Bao Feng Xu ◽  
Zhi Dan Lin ◽  
Jiang Ming Chen ◽  
Jun Lin
Keyword(s):  
Mechanical Properties ◽  
Thermal Conductivity ◽  
Thermal Properties ◽  
Graphene Nanoplatelets ◽  
Melt Blending ◽  
Blending Method

Graphene nanoplatelets (GNP) and nylon (PA) have been often used as thermal filler and matrix and respectively to produce composites. In this work, PA6/PA66/GNP thermal composites were prepared via a melt blending method. Mechanical properties, morphology, and thermal properties of PA6/PA66/GNP composites were investigated. Because the GNP is very expensive, we investigated to use Al2O3 and graphite and examined the characteristics of the prepared composites. Thermal conductivity values of PA6/PA66/GNP composites remarkably increased with increase of GNP contents mainly via layered dispersion in nylon matrix. The thermal conductivity of composite containing 50 wt % of GNP was measured as 5.03 W·m–1·K–1 at 30 °C, indicating an increase of more than 15 times compared with that of the neat PA6. When the Al2O3 was replaced for GNP, the thermal conductivity of composites decreased, but the mechanical properties improved. When graphite was used to replace for GNP, thermal conductivity basically remained unchanged but mechanical properties decreased.

Mechanical Properties of Poly(3-hydrobutyrate-co-hydroxyvalerate)/ Biodegradable Hyperbranched Poly(ester amide) Blends

2013 ◽  
Vol 745-746 ◽  
pp. 436-441
Author(s):  
Pei Liu ◽  
Long Chen ◽  
Jun Xu ◽  
Mei Fang Zhu ◽  
Zong Yi Qin
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Tensile Elongation ◽  
High Dispersion ◽  
Melt Blending ◽  
Elongation At Break ◽  
Biodegradable Composites ◽  
Hyperbranched Poly ◽  
Blending Method ◽  
Fracture Morphologies

Biodegradable composites were prepared by adding hyperbranched poly (ester amide) (HBPs) into poly (3-hydroxybutyrate-co-3-hydrovalerate) (PHBV) through melt blending method. It was found that the tensile strength and toughness of PHBV were simultaneously enhanced by the addition of HBPs. Compared with neat PHBV, the tensile strength of the composite increased about 23% from 20.96 to 25.87 MPa for the content of 2.5 wt.% HBPs, and more remarkable enhancement in tensile elongation at break can be achieved by about 88% for 5 wt.% HBPs. The influences of HBPs on crystallization, thermal and fracture morphologies of PHBV were further evaluated by using differential scanning calorimeter and scanning electron microscope, respectively. The decrease in the crystallinity of PHBV and high dispersion of the HBPs in PHBV matrix were observed, which should contribute to the improvement on the mechanical properties of PHBV.

Physical and Mechanical Properties of Thermoplastic Natural Rubber (TPNR) Nanocomposites

2012 ◽  
Vol 576 ◽  
pp. 394-397 ◽  
Author(s):  
Noor Azlina Hassan ◽  
Hassan Norita ◽  
Sahrim Haji Ahmad ◽  
Rozaidi Rasid ◽  
Hazleen Anuar ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Maleic Anhydride ◽  
Natural Rubber ◽  
Physical And Mechanical Properties ◽  
Melt Blending ◽  
Mixing Parameters ◽  
Blending Method ◽  
Thermoplastic Natural Rubber ◽  
Internal Mixer

Thermoplastic natural rubber (TPNR) nanocomposites were prepared by melt blending method with the optimum mixing parameters (140oC, 100 rpm, 12 min) using internal mixer (Haake 600 P). The aim of this work is to study the effects of organo-montmorillonite (OMMT) on the physical and mechanical properties of TPNR with and without coupling agent (maleic anhydride grafted polyethylene, MA-PE). Significant improvement in tensile strength and modulus of TPNR nanocomposites were obtained with the presence of MA-PE.

Effect of Ultrasonic Treatment on Morphology and Mechanical Properties of Bioplastic from Cassava Starch with Nanoclay Reinforcement

2017 ◽  
Vol 29 ◽  
pp. 35-41 ◽  
Author(s):  
Nanang Eko Wahyuningtiyas ◽  
Heru Suryanto
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Tensile Strength ◽  
Cassava Starch ◽  
Maximum Hardness ◽  
Blending Method ◽  
Sonication Treatment ◽  
Morphology And Mechanical Properties ◽  
Scanning Electron

The research is to investigate influence of sonication treatment on the morphologi and mechanical properties of bioplastic filler nanoclay with different nanoclay concentration. The bioplastic was prepared using blending method among bioplastic, glycerol, and nanoclay with assistance of sonication treatment of 30 mins. Structural characterization of bioplastic was examined using scanning electron microscopy (SEM), mechanical properties using durumeter Shore A, tensile strength and the physical properties using density. SEM evidence on a bioplastic basis. Hardness of bioplastic with addition of nanoclay 5.0% (b/b) and sonication treatment produce bioplastic with maximum hardness properties increased to 76.24 Shore A, tensile strength of 13.5 and Young’s modulus of 47, as well as the added density of 1.238 g/cm3. Nanoclay 7.5% (b/b) upwards will experience decreased hardness and experience agglomerate and debonding.

Effect of Blend Compositions on Mechanical Properties of Irradiated Titanium Dioxide (TiO2)/Polyvinyl Chloride (PVC)/Epoxidized Natural Rubber (ENR) Nanocomposites

2015 ◽  
Vol 1113 ◽  
pp. 43-49 ◽  
Author(s):  
Nur Azrini Ramlee ◽  
Siti Syuhadah Mohammad Hanapiah ◽  
Fatin Nabilah Suhaimi ◽  
Chantara Thevy Ratnam ◽  
Sivanesan Appadu
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Titanium Dioxide ◽  
Natural Rubber ◽  
Polyvinyl Chloride ◽  
Continuous Phase ◽  
Epoxidized Natural Rubber ◽  
Melt Blending ◽  
Scanning Microscope

In this study, effect of blend compositions of irradiated polyvinyl chloride (PVC)/epoxidized natural rubber (ENR) blends was carried out. In previous work, it was reported that the mechanical properties of 50/50 composition irradiated blend had performed the highest strength with addition of 6 wt% of titanium dioxide (TiO2). However, the combination of PVC/ENR in a certain ratio might results in optimal mechanical properties and other specific properties for the new blends formed. Thus, addition of 6 wt% TiO2 and varies compositional range of PVC/ENR ranging from 30, 50 and 70 wt% were prepared by melt-blending technique and the effects on the mechanical properties were investigated. The blends were exposed to 0-150 kGy of electron beam irradiation before being characterized. With addition of 6 wt% TiO2, the characterization of mechanical properties including tensile strength, impact and hardness shows increment in values for all compositions. The increments of tensile strength were fall within 6-18% and as expected 70/30 PVC/ENR blends have shown the highest value. Based on the result, it revealed tensile and impact strengths achieved the optimum value at 100 kGy, while hardness increased as the radiation dose increased. From scanning microscope electron (SEM), micrographs have illustrated the blends with addition of 6 wt% TiO2 are smooth, continuous phase and less void appearance were seen. At higher dose rate, fracture paths were found to be continuous and penetrate deep into the material and this indicates that the failure is essentially brittle and it supports the above findings.

Fabrication and Characterization of Biocomposite Using Grewia Optiva Fibre (i.e. Bhimal) Reinforced Polyvinyl Alcohol (PVA)

2015 ◽  
Vol 1105 ◽  
pp. 51-55 ◽  
Author(s):  
K.M. Gupta ◽  
Kishor Kalauni
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Natural Fibre ◽  
Fabrication Method ◽  
View Point ◽  
Engineering Material ◽  
Fibre Composites ◽  
Grewia Optiva ◽  
Fabrication And Characterization

Bhimal fibres are quite a newer kind of bio-degradable fibres. They have never been heard before in literatures from the view point of their utility as engineering material. These fibres have been utilized for investigation of their properties. Characterization of this fibre is essential to determine its properties for further use as reinforcing fibre in polymeric, bio-degradable and other kinds of matrix. With this objective, the fabrication method and other mechanical properties of Bhimal-reinforced-PVA biocomposite have been discussed. The stress-strain curves and load-deflection characteristics are obtained. The tensile, compressive, flexure and impact strengths have been calculated. The results are shown in tables and graphs. The results obtained are compared with other existing natural fibre biocomposites. From the observations, it has been concluded that the tensile strength of Bhimal-reinforced-PVA biocomposite is higher than other natural fibre composites. Hence these can be used as reinforcement to produce much lighter weight biocomposites.

scholarly journals Melt- vs. Non-Melt Blending of Complexly Processable Ultra-High Molecular Weight Polyethylene/Cellulose Nanofiber Bionanocomposite

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 404
Author(s):  
Nur Sharmila Sharip ◽  
Hidayah Ariffin ◽  
Tengku Arisyah Tengku Yasim-Anuar ◽  
Yoshito Andou ◽  
Yuki Shirosaki ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Yield Strength ◽  
Young’S Modulus ◽  
High Molecular Weight ◽  
Melt Processing ◽  
Cellulose Nanofiber ◽  
Melt Blending ◽  
Ultra High Molecular Weight

The major hurdle in melt-processing of ultra-high molecular weight polyethylene (UHMWPE) nanocomposite lies on the high melt viscosity of the UHMWPE, which may contribute to poor dispersion and distribution of the nanofiller. In this study, UHMWPE/cellulose nanofiber (UHMWPE/CNF) bionanocomposites were prepared by two different blending methods: (i) melt blending at 150 °C in a triple screw kneading extruder, and (ii) non-melt blending by ethanol mixing at room temperature. Results showed that melt-processing of UHMWPE without CNF (MB-UHMWPE/0) exhibited an increment in yield strength and Young’s modulus by 15% and 25%, respectively, compared to the Neat-UHMWPE. Tensile strength was however reduced by almost half. Ethanol mixed sample without CNF (EM-UHMWPE/0) on the other hand showed slight decrement in all mechanical properties tested. At 0.5% CNF inclusion, the mechanical properties of melt-blended bionanocomposites (MB-UHMWPE/0.5) were improved as compared to Neat-UHMWPE. It was also found that the yield strength, elongation at break, Young’s modulus, toughness and crystallinity of MB-UHMWPE/0.5 were higher by 28%, 61%, 47%, 45% and 11%, respectively, as compared to the ethanol mixing sample (EM-UHMWPE/0.5). Despite the reduction in tensile strength of MB-UHMWPE/0.5, the value i.e., 28.4 ± 1.0 MPa surpassed the minimum requirement of standard specification for fabricated UHMWPE in surgical implant application. Overall, melt-blending processing is more suitable for the preparation of UHMWPE/CNF bionanocomposites as exhibited by their characteristics presented herein. A better mechanical interlocking between UHMWPE and CNF at high temperature mixing with kneading was evident through FE-SEM observation, explains the higher mechanical properties of MB-UHMWPE/0.5 as compared to EM-UHMWPE/0.5.

scholarly journals A Comprehensive Investigation on 3D Printing of Polyamide 11 and Thermoplastic Polyurethane via Multi Jet Fusion

Polymers ◽  
2021 ◽  
Vol 13 (13) ◽  
pp. 2139
Author(s):  
Wei Shian Tey ◽  
Chao Cai ◽  
Kun Zhou
Keyword(s):  
Tensile Strength ◽  
Flexural Strength ◽  
Wear Rate ◽  
Mechanical Performance ◽  
Thermoplastic Polyurethane ◽  
Print Quality ◽  
Polyamide 11 ◽  
Powder Bed

Multi Jet Fusion (MJF) is a recently developed polymeric powder bed fusion (PBF) additive manufacturing technique that has received considerable attention in the industrial and scientific community due to its ability to fabricate functional and complex polymeric parts efficiently. In this work, a systematic characterization of the physicochemical properties of MJF-certified polyamide 11 (PA11) and thermoplastic polyurethane (TPU) powder was conducted. The mechanical performance and print quality of the specimens printed using both powders were then evaluated. Both PA11 and TPU powders showed irregular morphology with sharp features and had broad particle size distribution, but such features did not impair their printability significantly. According to the DSC scans, the PA11 specimen exhibited two endothermic peaks, while the TPU specimen exhibited a broad endothermic peak (116–150 °C). The PA11 specimens possessed the highest tensile strength in the Z orientation, as opposed to the TPU specimens which possessed the lowest tensile strength along the same orientation. The flexural properties of the PA11 and TPU specimens displayed a similar anisotropy where the flexural strength was highest in the Z orientation and lowest in the X orientation. The porosity values of both the PA11 and the TPU specimens were observed to be the lowest in the Z orientation and highest in the X orientation, which was the opposite of the trend observed for the flexural strength of the specimens. The PA11 specimen possessed a low coefficient of friction (COF) of 0.13 and wear rate of 8.68 × 10−5 mm3/Nm as compared to the TPU specimen, which had a COF of 0.55 and wear rate of 0.012 mm3/Nm. The PA11 specimens generally had lower roughness values on their surfaces (Ra < 25 μm), while the TPU specimens had much rougher surfaces (Ra > 40 μm). This investigation aims to uncover and explain phenomena that are unique to the MJF process of PA11 and TPU while also serving as a benchmark against similar polymeric parts printed using other PBF processes.

scholarly journals Fabrication and Characterization of Electrospun Polycaprolactone Blended with Chitosan-Gelatin Complex Nanofibrous Mats

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Yongfang Qian ◽  
Zhen Zhang ◽  
Laijiu Zheng ◽  
Ruoyuan Song ◽  
Yuping Zhao
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Weight Ratio ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Tissue Engineering Scaffolds ◽  
Elongation At Break ◽  
Nanofibrous Scaffolds ◽  
Two Peaks

Design and fabrication of nanofibrous scaffolds should mimic the native extracellular matrix. This study is aimed at investigating electrospinning of polycaprolactone (PCL) blended with chitosan-gelatin complex. The morphologies were observed from scanning electron microscope. As-spun blended mats had thinner fibers than pure PCL. X-ray diffraction was used to analyze the degree of crystallinity. The intensity at two peaks at 2θof 21° and 23.5° gradually decreased with the percentage of chitosan-gelatin complex increasing. Moreover, incorporation of the complex could obviously improve the hydrophilicity of as-spun blended mats. Mechanical properties of as-spun nanofibrous mats were also tested. The elongation at break of fibrous mats increased with the PCL content increasing and the ultimate tensile strength varied with different weight ratios. The as-spun mats had higher tensile strength when the weight ratio of PCL to CS-Gel was 75/25 compared to pure PCL. Both as-spun PCL scaffolds and PCL/CS-Gel scaffolds supported the proliferation of porcine iliac endothelial cells, and PCL/CS-Gel had better cell viability than pure PCL. Therefore, electrospun PCL/Chitosan-gelatin nanofibrous mats with weight ratio of 75/25 have better hydrophilicity mechanical properties, and cell proliferation and thus would be a promising candidate for tissue engineering scaffolds.

Thermoplastic polyurethane/CNT nanocomposites with low electromagnetic resistance property

2021 ◽  
pp. 002199832110370
Author(s):  
Chia-Fang Lee ◽  
Chin-Wen Chen ◽  
Fu-Sheng Chuang ◽  
Syang-Peng Rwei
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Thermoplastic Polyurethane ◽  
Conductive Polymer ◽  
Resistance Coefficient ◽  
Equal Weight ◽  
Mechanical And Thermal Properties ◽  
Multi Wall Carbon Nanotubes ◽  
Twin Screw ◽  
Acrylic Ester

Multi-wall carbon nanotubes (MWCNTs) at 0.5 wt% to 2 wt% proportions were added to thermoplastic polyurethane (TPU) synthesized with polycarbonatediol (PCDL), 4,4’-methylene diphenyl diisocyanate (MDI), and 1,3-butanediol(1,3-BDO). To formulate a new TPU-MWCNT nanocomposite, the composite was melt-blended with a twin-screw extruder. To ensure the even dispersion of MWCNTs, dispersant (ethylene acrylic ester terpolymer; Lotader AX8900) of equal weight proportion to the added MWCNTs was also added during the blending process. Studies on the mechanical and thermal properties, and melt flow experiments and phase analysis of TPU-MWCNT nanocomposites, these nanocomposites exhibit higher tensile strength and elongation at break than neat TPU. TPU-MWCNT nanocomposites with higher MWCNT content possess higher glass-transition temperature (Tg), a lower melt index, and greater hardness. Relative to neat TPU, TPU-MWCNT nanocomposites exhibit favorable mechanical properties. By adding MWCNTs, the tensile strength of the nanocomposites increased from 7.59 MPa to 21.52 MPa, and Shore A hardness increased from 65 to 81. Additionally, TPU-MWCNT nanocomposites with MWCNTs had lower resistance coefficients; the resistance coefficient decreased from 4.97 × 1011 Ω/sq to 2.53 × 104 Ω/sq after adding MWCNTs, indicating a conductive polymer material. Finally, the internal structure of the TPU-MWCNT nanocomposites was examined under transmission electron microscopy. When 1.5 wt% or 2 wt% of MWCNTs and dispersant were added to TPU, the MWCNTs were evenly dispersed, with increased electrical conductivity and mechanical properties. The new material is applicable in the electronics industry as a conductive polymer with high stiffness.

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