scholarly journals Optical Properties and Mechanical Modeling of Acetylated Transparent Wood Composite Laminates

Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2256
Author(s):  
Kyle E. O. Foster ◽  
Kristen M. Hess ◽  
Garret M. Miyake ◽  
Wil V. Srubar

Transparent wood composites (TWCs) are a new class of light-transmitting wood-based materials composed of a delignified wood template that is infiltrated with a refractive- index-matched polymer resin. Recent research has focused primarily on the fabrication and characterization of single-ply TWCs. However, multi-ply composite laminates are of interest due to the mechanical advantages they impart compared to the single ply. In this work, 1- and 2-ply [0°/90°] TWC laminates were fabricated using a delignified wood template (C) and an acetylated delignified wood template (AC). The optical and mechanical properties of resultant C and AC TWC laminates were determined using ultraviolet-visible spectroscopy (UV-Vis) and tensile testing (5× replicates), respectively. In addition, the ability of classical lamination plate theory and simple rule of mixtures to predict multi-ply tensile modulus and strength, respectively, from ply-level mechanical properties were investigated and are reported herein. Experimental results highlight tradeoffs that exist between the mechanical and optical responses of both unmodified and chemically modified TWCs. Template acetylation reduced the stiffness and strength in the 0° fiber direction by 2.4 GPa and 58.9 MPa, respectively, compared to the unmodified samples. At high wavelengths of light (>515 nm), AC samples exhibited higher transmittance than the C samples. Above 687 nm, the 2-ply AC sample exhibited a higher transmittance than the 1-ply C sample, indicating that thickness-dependent optical constraints can be overcome with improved interfacial interactions. Finally, both predictive models were successful in predicting the elastic modulus and tensile strength response for the 2-ply C and AC samples.

2019 ◽  
Vol 54 (11) ◽  
pp. 1497-1510 ◽  
Author(s):  
Ömer Bahadır Mergen ◽  
Ertan Arda ◽  
Gülşen Akın Evingür

In this work, chitosan/graphene nanoplatelets (CS/GNP) and chitosan/multi-walled carbon nanotube (CS/MWCNT) biocomposite films were prepared using a simple, eco-friendly and low-cost method. The electrical, optical and mechanical properties of these composite films were investigated. The optical, mechanical and electrical properties of the biocomposites were significantly improved, which make them promising materials for food packaging, ultraviolet protection and biomedical applications. With the increase of carbon filler content (GNP or MWCNT) in CS biocomposites, the surface conductivity ( σ), the scattered light intensity ( I sc) and the tensile modulus ( E) increased significantly. This behaviour in the electrical, optical and mechanical properties of the CS/carbon filler biocomposites was explained by percolation theory. The electrical percolation thresholds were determined as R σ = 25.0 wt.% for CS/GNP and R σ = 10.0 wt.% for CS/MWCNT biocomposites, while the optical percolation thresholds were found as R op =12.0 wt.% for CS/GNP and R op = 2.0 wt.% for CS/MWCNT biocomposites. Conversely, the mechanical percolation thresholds for both CS/GNP and CS/MWCNT biocomposites were found to be negligibly small ( R m = 0.0 wt.%). The electrical ( β σ), optical ( β op) and mechanical ( β m) critical exponents were calculated for both CS/carbon filler biocomposites and found compatible with the applied percolation theory.


2020 ◽  
Vol 54 (18) ◽  
pp. 2449-2459
Author(s):  
Ömer Bahadır Mergen ◽  
Ertan Arda ◽  
Gülşen Akın Evingür

In this study, we report the preparation of poly (methyl methacrylate)/multi-walled carbon nanotube (MWCNT) composite thin films by simple and efficient solution mixing and ultrasonic method and the electrical, optical, and mechanical characterizations. Scattered light intensity ( I sc), tensile modulus ( E), and surface conductivity ( σ) of these composites have increased with the addition of MWCNT into the composite. The observed behavior in electrical, optical, and mechanical properties of the poly (methyl methacrylate)/MWCNT composites was interpreted by site and classical percolation theory. The optical mechanical and electrical percolation thresholds of poly (methyl methacrylate)/MWCNT composites were determined as φ op = 3 wt%, φ m = 0 wt%, and φσ = 5 wt%, respectively. The optical ( t op), mechanical ( t m), and electrical ( t σ) critical exponents were calculated as 2.23, 0.43, and 0.11, respectively. Both the tensile modulus and tensile strength of poly (methyl methacrylate)/MWCNT composites were increased with increasing MWCNT content until it reaches to 10 wt%. However, above φ = 10 wt%, the mechanical properties of the composites were decreased due to the aggregation of MWCNTs, while the toughness does not show a significant change until φ = 10 wt% MWCNT content, whereas it was decreased above this value.


2014 ◽  
Vol 1025-1026 ◽  
pp. 215-220 ◽  
Author(s):  
Sasirada Weerasunthorn ◽  
Pranut Potiyaraj

Fumed silica particles (SiO2) were directly added into poly (butylene succinate) (PBS) by melt mixing process. The effects of amount of fumed silica particles on mechanical properties of PBS/fumed silica composites, those are tensile strength, tensile modulus, impact strength as well as flexural strength, were investigated. It was found that the mechanical properties decreased with increasing fumed silica loading (0-3 wt%). In order to increase polymer-filler interaction, fumed silica was treated with 3-glycidyloxypropyl trimethoxysilane (GPMS), and its structure was analyzed by FT-IR spectrophotometry. The PBS/modified was found to possess better tensile strength, tensile modulus, impact strength and flexural strength that those of PBS/fumed silica composites.


2020 ◽  
pp. 152808372097134
Author(s):  
Sherif M Youssef ◽  
M Megahed ◽  
Soliman S Ali-Eldin ◽  
MA Agwa

Vacuum resin infusion (VRI) is a promising technique for manufacturing complicated structural laminates. This high viscosity of nanofilled resin increases the filling time and leads to an incomplete mold filling. The mold filling time can be reduced either by making the fiber dimensions smaller than the mold (gaps around the fibers) or by adding ethanol to nanofilled epoxy. However, ethanol addition influences the mechanical properties of composite laminates. In this study, different amounts of ethanol (0.5 wt. % and 1 wt. %) were used as a diluent to both neat epoxy and epoxy filled with (0.25 wt. %) of titanium dioxide (TiO2) nanoparticles. From results, it was found that ethanol addition saves the time for neat and nanofilled epoxy by 47.1% and 24.1%, respectively. It was found that adding 0.5 wt. % of ethanol to 0.25wt. % of TiO2 nanoparticles (GT0.25E0.5) enhances the tensile and flexural strength by 30.8% and 55.9%, respectively compared with neat specimens. Furthermore, the tensile and flexural moduli increased by 62% and 72.3%, respectively. Furthermore, the mold filling time was investigated experimentally and validated numerically using ANSYS FLUENT software. The mold filling time prediction using ANSYS FLUENT can be used to avoid resin gelation before the incomplete mold filling and thus can be considered a cost-effective methodology. The results showed that the gaps around the fibers reduce the time by 178% without affecting the mechanical properties.


Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 698
Author(s):  
Selin Sökmen ◽  
Katja Oßwald ◽  
Katrin Reincke ◽  
Sybill Ilisch

High compatibility and good rubber–filler interactions are required in order to obtain high quality products. Rubber–filler and filler–filler interactions can be influenced by various material factors, such as the presence of processing aids. Although different processing aids, especially the plasticizers, and their effects on compatibility have been investigated in the literature, their influence on rubber–filler interactions in highly active filler reinforced mixtures is not explicit and has not been investigated in depth. For this purpose, the influence of treated distillate aromatic extract (TDAE) oil content and its addition time on interactions between silica and rubber chains were investigated in this study. Rubber–filler and filler–filler interactions of uncured and cured silica-filled SBR/BR blends were characterized by using rubber layer L concept and dynamic mechanical analysis, whereas mechanical properties were studied by tensile test and Shore A hardness. Five parts per hundred rubber (phr) TDAE addition at 0, 1.5, and 3 min of mixing were characterized to investigate the influence of TDAE addition time on rubber–filler interactions. It was observed that addition time of TDAE can influence the development of bounded rubber structure and the interfacial interactions, especially at short time of mixing, less than 5 min. Oil addition with silica at 1.5 min of mixing resulted in fast rubber layer development and a small reduction in storage shear modulus of uncured blends. The influence of oil content on rubber–filler and filler–filler interactions were investigated for the binary blends without oil, with 5 and 20 phr TDAE content. The addition of 5 phr oil resulted in a slight increase in rubber layer and 0.05 MPa reduction in Payne effect of uncured blends. The storage tensile modulus of vulcanizates at small strains decreased from 13.97 to 8.28 MPa after oil addition. Twenty parts per hundred rubber (phr) oil addition to binary blends caused rubber layer L to decrease from 0.45 to 0.42. The storage tensile modulus of the vulcanizates and its reduction with higher amplitudes were incontrovertibly high among the vulcanizates with lower oil content, which were 13.57 and 4.49 MPa, respectively. When any consequential change in mechanical properties of styrene–butadiene rubber (SBR)/butadiene rubber (BR) blends could not be observed at different TDAE addition time, increasing amount of oil in blends enhanced elongation at break, and decreased Shore A hardness and tensile strength.


2021 ◽  
Vol 56 (12) ◽  
pp. 7451-7463
Author(s):  
Yusheng Wang ◽  
Xiaowei Wu ◽  
Nahong Song ◽  
Xiaohui Yang ◽  
Yafeng Zheng ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Sahib Hasan ◽  
Khagendra Baral ◽  
Neng Li ◽  
Wai-Yim Ching

AbstractChalcogenide semiconductors and glasses have many applications in the civil and military fields, especially in relation to their electronic, optical and mechanical properties for energy conversion and in enviormental materials. However, they are much less systemically studied and their fundamental physical properties for a large class chalcogenide semiconductors are rather scattered and incomplete. Here, we present a detailed study using well defined first-principles calculations on the electronic structure, interatomic bonding, optical, and mechanical properties for 99 bulk chalcogenides including thirteen of these crytals which have never been calculated. Due to their unique composition and structures, these 99 bulk chalcogenides are divided into two main groups. The first group contains 54 quaternary crystals with the structure composition (A2BCQ4) (A = Ag, Cu; B = Zn, Cd, Hg, Mg, Sr, Ba; C = Si, Ge, Sn; Q = S, Se, Te), while the second group contains scattered ternary and quaternary chalcogenide crystals with a more diverse composition (AxByCzQn) (A = Ag, Cu, Ba, Cs, Li, Tl, K, Lu, Sr; B = Zn, Cd, Hg, Al, Ga, In, P, As, La, Lu, Pb, Cu, Ag; C = Si, Ge, Sn, As, Sb, Bi, Zr, Hf, Ga, In; Q = S, Se, Te; $$\hbox {x} = 1$$ x = 1 , 2, 3; $$\hbox {y} = 0$$ y = 0 , 1, 2, 5; $$\hbox {z} = 0$$ z = 0 , 1, 2 and $$\hbox {n} = 3$$ n = 3 , 4, 5, 6, 9). Moreover, the total bond order density (TBOD) is used as a single quantum mechanical metric to characterize the internal cohesion of these crystals enabling us to correlate them with the calculated properties, especially their mechanical properties. This work provides a very large database for bulk chalcogenides crucial for the future theoretical and experimental studies, opening opportunities for study the properties and potential application of a wide variety of chalcogenides.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1563
Author(s):  
Sofia Marquez-Bravo ◽  
Ingo Doench ◽  
Pamela Molina ◽  
Flor Estefany Bentley ◽  
Arnaud Kamdem Tamo ◽  
...  

Extremely high mechanical performance spun bionanocomposite fibers of chitosan (CHI), and cellulose nanofibers (CNFs) were successfully achieved by gel spinning of CHI aqueous viscous formulations filled with CNFs. The microstructural characterization of the fibers by X-ray diffraction revealed the crystallization of the CHI polymer chains into anhydrous chitosan allomorph. The spinning process combining acidic–basic–neutralization–stretching–drying steps allowed obtaining CHI/CNF composite fibers of high crystallinity, with enhanced effect at incorporating the CNFs. Chitosan crystallization seems to be promoted by the presence of cellulose nanofibers, serving as nucleation sites for the growing of CHI crystals. Moreover, the preferential orientation of both CNFs and CHI crystals along the spun fiber direction was revealed in the two-dimensional X-ray diffraction patterns. By increasing the CNF amount up to the optimum concentration of 0.4 wt % in the viscous CHI/CNF collodion, Young’s modulus of the spun fibers significantly increased up to 8 GPa. Similarly, the stress at break and the yield stress drastically increased from 115 to 163 MPa, and from 67 to 119 MPa, respectively, by adding only 0.4 wt % of CNFs into a collodion solution containing 4 wt % of chitosan. The toughness of the CHI-based fibers thereby increased from 5 to 9 MJ.m−3. For higher CNFs contents like 0.5 wt %, the high mechanical performance of the CHI/CNF composite fibers was still observed, but with a slight worsening of the mechanical parameters, which may be related to a minor disruption of the CHI matrix hydrogel network constituting the collodion and gel fiber, as precursor state for the dry fiber formation. Finally, the rheological behavior observed for the different CHI/CNF viscous collodions and the obtained structural, thermal and mechanical properties results revealed an optimum matrix/filler compatibility and interface when adding 0.4 wt % of nanofibrillated cellulose (CNF) into 4 wt % CHI formulations, yielding functional bionanocomposite fibers of outstanding mechanical properties.


2021 ◽  
pp. 096739112110239
Author(s):  
Sheedev Antony ◽  
Abel Cherouat ◽  
Guillaume Montay

Nowadays natural fibre composites have gained great significance as reinforcements in polymer matrix composites. Composite material based on a polymer matrix reinforced with natural fibres is extensively used in industry due to their biodegradability, recyclability, low density and high specific properties. A study has been carried out here to investigate the fibre volume fraction effect of hemp fibre woven fabrics/PolyPropylene (PP) composite laminates on the tensile properties and impact hammer impact test. Initially, composite sheets were fabricated by the thermal-compression process with desired number of fabric layers to obtain composite laminates with different fibre volume fraction. Uniaxial, shear and biaxial tensile tests were performed and mechanical properties were calculated. Impact hammer test was also carried out to estimate the frequency and damping parameters of stratified composite plates. Scanning Electron Microscope (SEM) analysis was performed to observe the matrix and fibre constituent defects. Hemp fabrics/PP composite laminates exhibits viscoelastic behaviour and as the fibre volume fraction increases, the viscoelastic behaviour decreases to elastic behaviour. Due to this, the tensile strength increases as the fibre content increases. On the other hand, the natural frequency increases and damping ratio decrease as the fibre volume fraction increases.


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