scholarly journals INFLUENCE OF COCONUT SHELL ADDITION ON PHYSICO-MECHANICAL PROPERTIES OF WOOD PLASTIC COMPOSITES1

2018 ◽  
Vol 41 (4) ◽  
Author(s):  
Éverton Hillig ◽  
Ignacio Bobadilla ◽  
Ademir José Zattera ◽  
Érick Agonso Agnes de Lima ◽  
Raquel Marchesan
Keyword(s):  
Mechanical Properties ◽  
Loblolly Pine ◽  
High Density Polyethylene ◽  
Wood Flour ◽  
High Density ◽  
Coconut Shell ◽  
Low Density Polyethylene ◽  
Low Density ◽  
Cellulosic Material ◽  
Thermoplastic Matrix

ABSTRACT In this study, composites with three types of thermoplastic matrix and cellulosic material in a proportion of 40% were produced. The three thermoplastic matrices were high density polyethylene (HDPE), polypropylene (PP) and low density polyethylene (LDPE), and the cellulosic materials were pure wood flour (Pinus taeda L) or a mixture of wood flour and coconut shell flour (Cocus nucifera L) in equal ratios. The objective was to evaluate the influence of addition of coconut shell on the physico-mechanical properties (density, strength and rigidity) and the distribution of the cellulosic material in the thermoplastic matrix of the manufactured composites. It was found that the composites had a satisfactory distribution of wood flour in thermoplastic matrices, but the addition of coconut shell promoted bubble formation in the resulting pieces and, thus, interfered with the material properties. The use of a coupling agent promoted interfacial adhesion (cellulose - thermoplastic matrix), which was better in high density polyethylene composites, followed by polypropylene and low density polyethylene. In general, the coconut shell addition caused a decrease of all properties compared to composites made with Loblolly Pine. In addition, the interactions between thermoplastic type and cellulosic matrix type have been statistically confirmed, which caused variations in the studied properties

Exploration on compatibilizing effect of nonionic, anionic, and cationic surfactants on mechanical, morphological, and chemical properties of high-density polyethylene/low-density polyethylene/cellulose biocomposites

2015 ◽  
Vol 30 (6) ◽  
pp. 855-884 ◽  
Author(s):  
AK Sudari ◽  
AA Shamsuri ◽  
ES Zainudin ◽  
PM Tahir
Keyword(s):  
Mechanical Properties ◽  
High Density Polyethylene ◽  
Sodium Stearate ◽  
High Density ◽  
Low Density Polyethylene ◽  
Hexadecyltrimethylammonium Bromide ◽  
Low Density ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Compatibilizing Effect

Three types of surfactants, specifically cationic, anionic, and nonionic, at different weight percentages were added into high-density polyethylene/low-density polyethylene/cellulose (HDPE/LDPE/cellulose) biocomposites via melt mixing. The cationic and anionic surfactants which are hexadecyltrimethylammonium bromide (HTAB) and sodium stearate (SS), respectively, were added from 4 to 20 wt%, whereas the nonionic surfactant which is sorbitan monostearate (SM) was added from 1 to 5 wt%. The mechanical testing results exhibited that the addition of HTAB increased tensile strength and tensile modulus, while SS deteriorated mechanical properties, while SM increased impact strength and tensile extension of the biocomposites. Based on the mechanical properties results, optimum weight percentages of HTAB and SM were 12 wt% and 4 wt%, respectively. The scanning electron microscopic micrographs displayed that the amount of cellulose fillers pullout decreased with the addition of HTAB, followed by SM, but it increased with SS. Fourier transform infrared spectra, X-ray diffractometer patterns, thermogravimetric analysis results, and differential scanning calorimetry thermograms have confirmed the presence of physical interactions only with the addition of HTAB and SM. Based on the results, compatibilizing effect was found in HTAB, whereas SM has not showed compatibilizing effect but instead plasticizing effect. However, neither compatibilizing nor plasticizing effect was exhibited by SS.

Influence of organically modified nanoclay and TiO2 nanopowder on the properties of Azadirachta indica wood flour-reinforced high-density polyethylene, low-density polyethylene, polypropylene, and polyvinyl chloride nanocomposite

2020 ◽  
pp. 089270572093596
Author(s):  
Vamsi Rathnam ◽  
Arenjungla Kichu ◽  
Nipu Dutta ◽  
Tarun K Maji ◽  
Nirmala Devi
Keyword(s):  
Azadirachta Indica ◽  
High Density Polyethylene ◽  
Wood Flour ◽  
High Density ◽  
Low Density Polyethylene ◽  
Ammonium Bromide ◽  
Mechanical And Thermal Properties ◽  
Low Density ◽  
Xrd Study ◽  
Organically Modified

The nanocomposites of high-density polyethylene, low-density polyethylene, polypropylene, and poly(vinyl chloride) reinforced with Azadirachta indica wood flour (WF) and different amounts of the organomodified nanoclay and titanium dioxide (TiO2) nanopowder were produced by melt-blending process followed by compression molding. Polyethylene- co-glycidyl methacrylate (PE- co-GMA) was used as a compatibilizer. TiO2 nanopowder was synthesized by sol–gel method and characterized using transmission electron microscopy (TEM). The average size of the synthesized nano-TiO2 was 17.5 nm, which was confirmed both by TEM and X-ray diffraction (XRD) study. The distribution of nanoparticles in the nanocomposites was also examined by the XRD study. The surface modification of the TiO2 nanoparticles by organic surfactant cetyl trimethyl ammonium bromide and their interaction with the wood and the polymer were studied by Fourier transform infrared spectroscopy. Incorporation of compatibilizer PE- co-GMA, nanoclay, and nano-TiO2 significantly influenced the mechanical and thermal properties of the WF-reinforced composites. Wood polymer composites (WPC) reinforced with nanoclay and nano-TiO2 showed improved tensile strength, tensile modulus, flexural strength, flexural modulus, and hardness. Maximum improvement in mechanical properties was shown by WPC loaded with 40 phr WF, 2 phr nanoclay, and 2 phr of nano-TiO2. On inclusion of organically modified nanoclay and nano-TiO2, the WPC samples showed lower water uptake and higher chemical resistance. The nanocomposites were further examined by TEM study and thermogravimetric analyzer.

scholarly journals Low-Temperature Mechanical Properties of High-Density and Low-Density Polyethylene and Their Blends

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1821
Author(s):  
Ildar I. Salakhov ◽  
Nadim M. Shaidullin ◽  
Anatoly E. Chalykh ◽  
Mikhail A. Matsko ◽  
Alexey V. Shapagin ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Low Temperature ◽  
Impact Strength ◽  
Relative Elongation ◽  
High Density ◽  
Low Density Polyethylene ◽  
Low Density ◽  
Elongation At Break ◽  
Subzero Temperatures ◽  
Izod Impact

Low-temperature properties of high-density polyethylene (HDPE), low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), and their blends were studied. The analyzed low-temperature mechanical properties involve the deformation resistance and impact strength characteristics. HDPE is a bimodal ethylene/1-hexene copolymer; LDPE is a branched ethylene homopolymer containing short-chain branches of different length; LLDPE is a binary ethylene/1-butene copolymer and an ethylene/1-butene/1-hexene terpolymer. The samples of copolymers and their blends were studied by gel permeation chromatography (GPC), differential scanning calorimetry (DSC), 13С NMR spectroscopy, and dynamic mechanical analysis (DMA) using testing machines equipped with a cryochamber. It is proposed that such parameters as “relative elongation at break at −45 °C” and “Izod impact strength at −40 °C” are used instead of the ductile-to-brittle transition temperature to assess frost resistance properties because these parameters are more sensitive to deformation and impact at subzero temperatures for HDPE. LLDPE is shown to exhibit higher relative elongation at break at −45 °C and Izod impact strength at −20 ÷ 60 °C compared to those of LDPE. LLDPE terpolymer added to HDPE (at a content ≥ 25 wt.%) simultaneously increases flow properties and improves tensile properties of the blend at −45 °C. Changes in low-temperature properties as a function of molecular weight, MWD, crystallinity, and branch content were determined for HDPE, LLDPE, and their blends. The DMA data prove the resulting dependences. The reported findings allow one to understand and predict mechanical properties in the HDPE–LLDPE systems at subzero temperatures.

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