A novel two-step melt blending method to prepare nano-silanized-silica reinforced crosslinked polyethylene (XLPE) nanocomposites

2022 ◽  
Author(s):  
Yasir Qayyum Gill ◽  
Hira Ehsan ◽  
Umer Mehmood ◽  
Muhammad Shafiq Irfan ◽  
Farhan Saeed
Keyword(s):  
Melt Blending ◽  
Blending Method ◽  
Silanized Silica

Mechanical, Thermal, and Morphological Properties of Thermoplastic Starch/Poly(lactic acid/Poly(butylene adipate-co-terephthalate) Blends

2014 ◽  
Vol 970 ◽  
pp. 312-316
Author(s):  
Sujaree Tachaphiboonsap ◽  
Kasama Jarukumjorn
Keyword(s):  
Lactic Acid ◽  
Impact Strength ◽  
Interfacial Adhesion ◽  
Tensile Modulus ◽  
Thermoplastic Starch ◽  
Morphological Properties ◽  
Poly Lactic Acid ◽  
Melt Blending ◽  
Elongation At Break ◽  
Blending Method

Thermoplastic starch (TPS)/poly (lactic acid) (PLA) blend and thermoplastic starch (TPS)/poly (lactic acid) (PLA)/poly (butylene adipate-co-terephthalate) (PBAT) blend were prepared by melt blending method. PLA grafted with maleic anhydride (PLA-g-MA) was used as a compatibilizer to improve the compatibility of the blends. As TPS was incorporated into PLA, elongation at break was increased while tensile strength, tensile modulus, and impact strength were decreased. Tensile properties and impact properties of TPS/PLA blend were improved with adding PLA-g-MA indicating the enhancement of interfacial adhesion between PLA and TPS. With increasing PBAT content, elongation at break and impact strength of TPS/PLA blends were improved. The addition of TPS decreased glass transition temperature (Tg), crystallization temperature (Tc), and melting temperature (Tm) of PLA. Tgand Tcof TPS/PLA blend were decreased by incorporating PLA-g-MA. However, the presence of PBAT reduced Tcof TPS/PLA blend. Thermal properties of TPS/PLA/PBAT blends did not change with increasing PBAT content. SEM micrographs revealed that the compatibilized TPS/PLA blends exhibited finer morphology when compared to the uncompatibilized TPS/PLA blend.

Thermal Stability and Crystallization Behavior of PP/Organoclay Phase Change Composites

2013 ◽  
Vol 785-786 ◽  
pp. 123-126
Author(s):  
Ying Ye ◽  
Kun Yan Wang ◽  
Ge Chang ◽  
Qian Ying Jiang
Keyword(s):  
Thermal Stability ◽  
Phase Change ◽  
Crystallization Behavior ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
Nucleation Agent ◽  
Scanning Calorimetry ◽  
Blending Method ◽  
Phase Change Composites ◽  
Change Material

Polypropylene/organoclay modified by dodecanol phase change material were prepared by melt blending method. The thermal stability and crystallization behavior was studied by thermogravimetry (TG), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). TG results indicated the window of processing of PP could be improved by adding small amount organoclay modified by dodecanol to the blend. DSC showed the organoclay modified by dodecanol affected the crystallization behavior of PP as heterogeneous nucleation agent. XRD results show that the organoclay modified by dodecanol does not change the crystal structure in the blends but only decrease the intensity of the diffraction peak.

Effect of magnesium oxysulfate (MOS) morphology on the crystallization, mechanical, and rheological properties of polypropylene/MOS composites

2018 ◽  
Vol 32 (5) ◽  
pp. 710-726 ◽  
Author(s):  
Li Dang ◽  
Xueying Nai ◽  
Xin Liu ◽  
Zhihui Lv ◽  
Wu Li
Keyword(s):  
Rheological Properties ◽  
Polarized Light ◽  
Mechanical Tests ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
Small Amplitude Oscillatory Shear ◽  
Blending Method ◽  
Magnesium Oxysulfate ◽  
Significant Yield ◽  
The Impact

Polypropylene (PP) composites containing magnesium oxysulfate particle (MOSp), magnesium oxysulfate whisker (MOSw), or magnesium oxysulfate sector (MOSs) were prepared via melt blending method. Scanning electron microscopy results showed that three magnesium oxysulfate (MOS) fillers all dispersed homogeneously in PP matrix and displayed vague and fuzzy interfaces. Wide-angle X-ray diffraction (WXRD) patterns showed that MOSp induced the most amount of β-PP, which was supported by polarized light microscopy (PLM) photographs. Moreover, PLM photographs also showed that the presence of MOSp, MOSw, or MOSw decreased the PP spherulites, especially for MOSp. As such, mechanical tests showed that incorporation of MOSp into PP matrix greatly improved the impact strength and least lowered the nominal strain at break. The yield strength and Young’s modulus of composites were greatly enhanced with MOSw. Two possible reasons for this phenomenon are rigidity of MOSw and microstructure of composites. Rheological properties were measured via small amplitude oscillatory shear. The results showed that PP melts containing MOSw exhibited significant yield stress and “shear-thinning” behaviors, which indicated the formation of MOSw network and the transition from “liquid-like” PP matrix to “solid-like” composites. The rheological results greatly proved the enhancement in tensile properties of MOSw-incorporated composites.

Preparation and Characterization of Flame Retardant PET Fiber via Melt Blending

2018 ◽  
Vol 913 ◽  
pp. 729-737
Author(s):  
Hui Ling Xu ◽  
Hong Kun Bao ◽  
Chao Sheng Wang ◽  
Hua Ping Wang
Keyword(s):  
Flame Retardant ◽  
Ethylene Terephthalate ◽  
Carbon Layer ◽  
Melt Blending ◽  
Fiber Fracture ◽  
Limiting Oxygen Index ◽  
Poly Ethylene Terephthalate ◽  
Blending Method ◽  
Poly Ethylene

Poly(ethylene terephthalate) (PET) fiber with excellent flame retardant property was prepared with introducing a containing phosphorus flame retardant 10-(2’,5’-dihydroxyphenyl) -9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (ODOPB) into PET by melt blending method. The intrinsic viscosity of the modified PET was decreased after melt blending, indicated that ODOPB could promote the degradation of PET. The addition of ODOPB can increase the amount of carbon residue of PET, which can effectively reduce the heat transfer. The movement and regularity of PET molecular chain are affected by ODOPB, resulting in the reducing of the crystallization of PET. The Raman curves indicate that the addition of ODOPB can improve the regularity of carbon layer, which is conducive to achieve the effect of flame retardant. When the mass fraction of P is 0.7 %, the limiting oxygen index of sample reaches 32.4% and UL-94 vertical reaches V-2, the fiber fracture strength is 2.6 cN/dtex, which has excellent flame retardant and mechanical properties.

Effect Addition of Octadecylamine Modified Clay (ODA-MMT) to Polylactide/Polycaprolactone (PLA/PCL) Blend

2011 ◽  
Vol 364 ◽  
pp. 317-321 ◽  
Author(s):  
Siti Zulaiha Hairaldin ◽  
Wan Md Zin Wan Yunus ◽  
Nor Azowa Ibrahim
Keyword(s):  
Polymer Nanocomposite ◽  
Average Diameter ◽  
Sem Analysis ◽  
Clay Nanocomposites ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
X Ray ◽  
Blending Method ◽  
Sem Micrograph ◽  
Internal Mixer

In this study, Octadecylamine Modified montmorillonites (ODAMMT) were used to prepare polylactide/polycaprolactone (PLA/PCL) clay nanocomposites. PLA and PCL were blend using an internal mixer by melt blending method. The other sample was blend with natrium monmorillonite (NaMMT) and Octadecylamine modified monmorillonite to produce PLA/PCL-NaMMT and PLA/PCL-ODAMMT. To characterize the polymer nanocomposite, X-ray diffraction (XRD), FTIR and SEM analysis were conducted. Comparison of morphology were made up between neat PLA/PCL, PLA/PCL with presence of of montmorillonite and octadecylamine modified monmorillonite respectively based on SEM micrograph. The number-average diameter was calculated for PLA/PCL, PLA/PCL-NaMMT, and PLA/PCL-ODAMMT.

Preparation and Property Study of PMMA/ASA Alloy

2011 ◽  
Vol 130-134 ◽  
pp. 2383-2387
Author(s):  
Guo Dong Tang ◽  
Si Chen ◽  
Yan Qin Shi ◽  
Xu Wang
Keyword(s):  
Flow Rate ◽  
Melt Blending ◽  
Dsc Analysis ◽  
Melt Flow ◽  
Scanning Calorimetry ◽  
Melt Flow Rate ◽  
Interface Phase ◽  
Blending Method ◽  
Method Effects ◽  
The Impact

Polymethyl methacrylate (PMMA)/ acrylonitrile-styrene-acrylate terpolymer (ASA) alloy was prepared via melt blending method. Effects of ASA melt flow rate and PMMA/ASA ratio on mechanical property of the alloy were studied. It showed that when the high melt flow rate ASA was used, alloy’s tensile strength and flexural strength were little different from using low melt flow rate ASA, while the impact strength was significantly higher than the latter. Differential scanning calorimetry (DSC) analysis showed that a glass transition (Tg) platform emerged in low melt flow rate ASA at 48.5°C, which represented the Tg of the interface phase formed between SAN grafted acrylate rubber particles and SAN matrix. Scanning electron microscope (SEM) experiment further showed that when low melt flow rate ASA was used, alloy’s cross section was smooth which showed the characteristics of brittle fracture.

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.

Compatibilized PP/EPDM-Kenaf Fibre Composite Using Melt Blending Method

2011 ◽  
Vol 264-265 ◽  
pp. 743-747 ◽  
Author(s):  
Hazleen Anuar ◽  
N.A. Hassan ◽  
F. Mohd Fauzey
Keyword(s):  
Fibre Composite ◽  
Thermoplastic Elastomer ◽  
Hibiscus Cannabinus ◽  
Melt Blending ◽  
Scanning Electron Micrograph ◽  
Kenaf Fiber ◽  
Fiber Loading ◽  
Kenaf Fibre ◽  
Blending Method ◽  
Internal Mixer

Thermoplastic Elastomer (TPE) composite reinforced with Hibiscus cannabinus, L fiber (kenaf fiber, KF) was prepared via melt blending method using internal mixer at temperature 180°C, screw rotational speed at 40rpm for 10 min. TPE matrix is a blend of polypropylene (PP) and ethylene-propylene-diene monomer (EPDM) at a ratio of 70:30. The optimum fiber loading were investigated from 0% to 20% by volume. The effect of coupling agent maleic anhydride polypropylene (MAPP) on the TPE composite has been investigated. The result shown that, with increasing the kenaf fiber content gradually increased the tensile strength and flexural strength for both treated and untreated PP/EPDM-KF composite. However, at 20% of kenaf fiber loading, it showed decreasing in impact strength due to brittleness of the samples. From the scanning electron micrograph (SEM) it has shown that the composite, with compatibilizer promotes better interaction between TPE and kenaf fiber.

Crystallization Behavior and Crystal Morphology of PP/POEg Blends

2014 ◽  
Vol 941-944 ◽  
pp. 1253-1256
Author(s):  
Kun Yan Wang
Keyword(s):  
Crystallization Behavior ◽  
Crystal Morphology ◽  
Optical Microscope ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Blending Method ◽  
Differential Scanning Colorimetry ◽  
Poly Ethylene ◽  
Spherulitic Structure

Polypropylene (PP)/Maleic anhydride grafted poly (ethylene-octene) (POEg) were prepared by melt blending method. The crystallization behavior and crystal morphology were studied by differential scanning calorimetry (DSC), X-ray diffraction (XRD), and polarzing optical microscope (POM). Differential scanning colorimetry (DSC) experiments showed that the melting point and crystallization point decreased when POEg added to the blend. XRD results show that the POEg not change the crystal structure in the blends but only decrease the intensity of the diffraction peak. The spherulitic structure could also observed when added POEg to the matix of PP, but the shape of the spherulites distorted.

Mechanical and morphological properties of high density polyethylene and polylactide blends

2014 ◽  
Vol 34 (9) ◽  
pp. 813-821 ◽  
Author(s):  
Gaurav Madhu ◽  
Haripada Bhunia ◽  
Pramod K. Bajpai ◽  
Veena Chaudhary
Keyword(s):  
High Density Polyethylene ◽  
High Density ◽  
Morphological Properties ◽  
Heat Of Fusion ◽  
Melt Blending ◽  
Scanning Calorimetry ◽  
Elongation At Break ◽  
Blown Film ◽  
Blending Method ◽  
Spectroscopy Studies

Abstract Polyblend films were prepared from high-density polyethylene (HDPE) and poly(l-lactic acid) (PLLA) up to 20% PLLA by the melt blending method in an extrusion mixer with post-extrusion blown film attachment. The 80/20 (HDPE/PLLA) blend was compatibilized with maleic anhydride grafted polyethylene (PE-g-MA) in varying ratios [up to 8 parts per hundred of resin (phr)]. Tensile properties of the films were evaluated to obtain optimized composition for packaging applications of both non-compatibilized and compatibilized blends. The compositions HDPE80 (80% HDPE and 20% PLLA) and HD80C4 (80% HDPE, 20% PLLA and 4 phr compatibilizer) were found to be optimum for packaging applications. However, better tensile strength (at yield) and elongation (at break) of 80/20 (HDPE/PLLA) blend were noticed in the presence of PE-g-MA. Further, thermal properties and morphologies of these blends were evaluated. Differential scanning calorimetry (DSC) study revealed that blending does not much affect the crystalline melting point of HDPE and PLLA, but heat of fusion of 80/20 (HDPE/PLLA) blend was decreased as compared to that of neat HDPE. Spectroscopy studies showed evidence of the introduction of some new groups in the blends and gaining compatibility in the presence of PE-g-MA. The compatibilizer influenced the morphology of the blends, as apparent from scanning electron microscopy (SEM) and supported by Fourier transform infrared (FTIR).

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