Effect of Wood Flour Content on the Thermal,Mechanical and Dielectric Properties of Poly(vinyl chloride)

Several composite formulations of poly(vinyl chloride)/olive wood flour (PVC/WF) were manufactured by dry‐blending PVC, wood flour, plasticizer and other processing additives in a high‐intensity mixer. The dry‐blended compounds were calendered into film samples (T = 180°C, calendered time = 8 min). The films obtained are cut into normalized samples for thermal, mechanical, and dielectric characterization. The results obtained show that stress as well as strain at break decrease sharply as the wood flour content increases. On the other hand, this filler content has little influence on the glass transition temperature. It decreases the temperature of decomposition setting and retards the PVC thermal decomposition. It increases permittivity as well as dielectric losses. The thermal stability, as measured by thermogravimetry (TGA) and differential scanning calorimetry (DSC) methods, is good enough to permit processing of these types of PVC compounds using conventional processing techniques and temperatures under 210°C.     

Coextruded PVC/wood‐flour composites with WPC cap layers

Wood‐plastic composites (WPCs) can absorb moisture in a humid environment owing to the hydrophilic nature of the wood, thereby making the products susceptible to microbial growth and loss of mechanical properties. In this study, rigid poly(vinyl chloride) (PVC)/wood‐flour composites (core layer) were coextruded with either unfilled rigid PVC (cap layer) or rigid PVC filled with a small amount (5–27.5%) of wood flour (composite cap layers) in order to decrease or delay the moisture uptake. The thickness of the cap layer and its composition in terms of wood flour content were the variables examined during coextrusion. Surface color, moisture absorption, and flexural properties of both coextruded and noncoextruded (control) composite samples were characterized. The experimental results indicated that both unfilled PVC and composite cap layers can be encapsulated over rigid PVC/wood‐flour composites in a coextrusion process. The moisture uptake rate was lower when a cap layer was applied in the composites, and the extent of the decrease was a strong function of the amount of wood flour in the cap layer but insensitive to cap layer thickness. Overall, coextruding PVC surface‐rich cap layers on WPCs significantly increased the flexural strength but decreased the flexural modulus as compared with those of control samples. The changes in bending properties were sensitive to both cap layer thickness and wood flour content. J. VINYL ADDIT. TECHNOL., 2008. © 2008 Society of Plastics Engineers     

Accelerated ultraviolet weathering of PVC/wood‐flour composites

Ultraviolet weathering performance of polyvinyl chloride (PVC) filled with different concentrations of wood flour was studied. Extruded PVC/wood‐flour composite samples were subjected to cyclic ultraviolet lamps/condensation exposures and assessed over a total of 400 and 2600 hours. Each assessment consisted of DRIFTFTIR and XPS collections, contact angle measurement, color measurement, and tensile property testing. The experimental results indicated that wood flours are effective chromophore materials since their incorporation into a rigid PVC matrix accelerated the degradation of the polymeric matrix. Photodegradation converted unfilled PVC samples to a colored material of lower extensibility. Although composite samples exhibited greater discoloration than unfilled PVC samples, they retained all their original strength and stiffness properties even after 2600 hours of cyclic UV irradiation/condensation exposures.     

Wood flour: A new filler for the rubber processing industry. I. Cure characteristics and mechanical properties of wood flour‐filled NBR and NBR/PVC compounds

In this study, conifer wood flour was evaluated as a filler to NBR or NBR/PVC compounds studying it influence on their cure characteristics and mechanical properties. It was shown that the filling by wood flour offers a possibility to obtain high modulus high elastic or less elastic or rigid wood like vulcanizates by varying of both the filling level and NBR/PVC mass ratio.It was established that in contrary to the mineral fillers usually causing significant delay of the vulcanization process, the wood flour shows a tendency to reduce the optimum cure time, τ₉₀. Modulus M₁₀₀ and Shore hardness of the wood flour‐filled vulcanizates of NBR or NBR/PVC compounds in which NBR is predominant, increase in a compliance with the increase of M_max and DM when the filling level increases. The dependence is other when NBR and PVC are in equal amounts or PVC predominates. As a most probable explanation of the effect of the wood flour on the cure characteristics is accepted, the influence of the wood flour polar groups as well as of the presenting as wood flour humidity water molecules, the specific mechanical properties of the wood flour‐filled NBR or NBR/PVC compounds could be connected (to some extend) with a specific interface interaction between the wood flour particles and the polymer matrix. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2734–2739, 2003     

Thermal degradation and ageing behavior of microcomposites of natural rubber,carboxylated styrene butadiene rubber latices,and their blends

The effect of microfillers on the thermal stability of natural rubber (NR), carboxylated styrene butadiene rubber (XSBR) latices, and their 70/30 NR/XSBR blend were studied using thermogravimetric method. Microcomposites of XSBR and their blend were found to be thermally more stable than unfilled samples. The activation energy needed for the degradation of polymer chain was calculated from Coats‐Redfern plot. Activation energy needed for the thermal degradation of filled samples was higher than unfilled system. It indicated the improved thermal stability of the filled samples. The ageing resistance of the micro‐filled samples was evaluated from the mechanical properties of aged samples. The thermal ageing was carried out by keeping the samples in hot air oven for 7 days at 70°C. The mechanical properties such as tensile strength, modulus at 300% elongation, and strain at break were computed. As compared to unfilled samples, micron‐sized fillers reinforced systems exhibited higher ageing resistance. Finally, an investigation was made on the influence of ion‐beam irradiation on microcomposites of NR, XSBR latices, and their 70/30 blend systems using ²⁸Si⁸⁺ performed at 100 MeV. The surface changes of the samples after irradiation were analyzed using X‐ray photoelectron spectroscopy. The results of XPS measurements revealed that the host elements were redistributed without any change in binding energies of C_1s, O_1s, and Si_2p. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Durability of wood flour‐plastic composites exposed to accelerated freeze–thaw cycling. Part I. Rigid PVC matrix

This study examined the effects of accelerated freeze–thaw actions on the durability of wood fiber‐plastic composites. Rigid PVC formulations filled with various concentrations of wood flour (both pine and maple) were processed in a counterrotating twin‐screw extruder and exposed to cyclic freeze–thaw actions according to ASTM Standard D6662. Freeze–thaw cycling was also modified by omitting portions of the test (either the water or freezing) to verify whether or not moisture was the primary cause for property loss. The durability of exposed samples was assessed in terms of flexural properties, density, and dimensional stability. Scanning electron micrographs of unexposed and freeze–thaw‐exposed samples were taken to qualitatively evaluate the interfacial adhesion between the wood flour and PVC matrix. The experimental results indicated that the density was not affected by freeze–thaw cycling. The dimensional stability was also relatively unaffected, although greater wood flour content exhibited greater dimensional change. The loss in stiffness of the composites was statistically significant after only two freeze–thaw cycles, regardless of both the wood species and content. Conversely, the strength of the composites was not significantly affected by five freeze–thaw cycles at lower wood flour contents (50 and 75 phr). The deleterious effects of the freeze–thaw actions on the strength of the composites became apparent at higher wood flour content (100 phr) after only two freeze–thaw cycles for maple flour and five freeze–thaw cycles for pine flour. The property loss was attributed primarily to the water portion of the cycling, which appears to have led to the decreased interfacial adhesion between the wood flour and the rigid PVC matrix. J. VINYL. ADDIT. TECHNOL. 11:1–8, 2005. © 2005 Society of Plastics Engineers.     

Calcium carbonate and wood reinforced hybrid PVC composites

In this article, poly(vinyl chloride) (PVC) sandwich‐structured hybrid composites with amorphous calcium carbonate and wood‐filled cores were obtained by compression molding. It has been determined that wood addition up to a weight ratio of 33% reported to the total filler amount is beneficial in improving both the inter‐filler and filler‐matrix interfacial adhesion, which alongside with the promoting of the amorphous PVC matrix crystallization is responsible for an increase up to 34% in the flexural strength of the composites, compared to unfilled PVC. The hybrid filled composites present up to 35% lower friction coefficients and up to 20% higher Brinell hardness values than the composites filled with calcium carbonate alone. Subsequently, wood addition determines an increase in the oxidation onset temperature for PVC and an increase with up to 20% in the sound and thermal‐insulative properties of the composites, compared to unfilled PVC. The dominating dispersive part of the composites surface energy aids in improving the mass and dimensional stability of the assembly to both water and dilute hydrochloric acid aqueous solutions. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46317.     

Online measurement of rheological properties of PVC/wood‐flour composites

By using a factorial design approach, this study examined the effect of the component materials on the viscoelastic properties of PVC/wood‐flour composites. Statistical analysis was performed to determine the effects of wood‐flour content, acrylic modifier content, and plasticizer content on the die swell ratio and viscosity of the composites measured online on a conical twin‐screw extrusion capillary rheometer. The viscoelastic properties of the samples also were measured using dynamic mechanical analyzer (DMA). Wood‐flour content and acrylic modifier content were the two important variables affecting the die swell ratio, whereas the addition of a low level of plasticizer did not affect this ratio. The die swell increased with the increased acrylic modifier content, but it was reduced considerably by adding wood flour into the PVC matrix. The true viscosity of neat PVC and PVC/wood‐flour composites decreased with the plasticizer content, irrespective of the acrylic modifier content. However, the addition of acrylic modifier significantly increased the viscosity of unfilled PVC, while an opposite trend was observed for the composites, owing to the differing effect of acrylic modifier on the melt elasticity and viscosity of these materials. J. Vinyl Addit. Technol. 10:121–128, 2004. © 2004 Society of Plastics Engineers.     

Effects of copper amine treatment on mechanical properties of PVC/wood‐flour composites

Copper amine–treated wood flour was added to PVC [poly(vinyl chloride)] matrix in order to manufacture PVC/wood‐flour composites. Effects of copper treatments on the mechanical properties of PVC‐wood composites were evaluated. Unnotched impact strength, flexural strength, and flexural toughness of the composites were significantly improved by the wood‐flour copper treatment. The optimum copper concentration range was 0.2 to 0.6 wt% of wood flour. Fractured surfaces were examined by using scanning electron microscopy (SEM) combined with energy‐dispersive spectroscopy (EDS). PVC/wood interfacial debonding was the main fracture mode of untreated wood‐flour composites, whereas wood‐particle pullout and breakage dominating the fractured surfaces of copper‐treated wood‐flour composites. On the fractured surfaces, more PVC could be found on the exposed copper‐treated wood particles than on untreated wood, a result suggesting improved PVC‐wood interfacial adhesion after copper treatments. J. Vinyl Addit. Technol. 10:70–78, 2004. © 2004 Society of Plastics Engineers.     

Effect of compatibilizers on water absorption kinetics of polypropylene/wood flour foamed composites

Polypropylene (PP)/wood flour foamed composites were prepared by taking PP:wood flour in the ratios of 100 : 0, 90 : 10, 80 : 20, 70 : 30, and 60 : 40 (w/w), with and without compatibilizers like maleic anhydride‐treated wood flour and maleic anhydride‐grafted PP (PPgMA). The foamed composite samples were employed for water swelling at 27°C, 70°C, and in steam. The absorption of water increased with increase in filler contents for all three‐temperature conditions. The maleic anhydride‐treated wood flour and PPgMA showed reduction in water swelling, and the best one was in case of the PPgMA‐foamed composites for respective conditions. Diffusion, sorption, and permeation coefficients were determined to study the absorption kinetics. FTIR spectra were also recorded for 30 wt % of filler loading for all the composites, which showed the effect of compatibilizers on reduction in water absorption in foamed PP/wood flour composites. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2530–2537, 2006     

Novel coupling agents for PVC/wood‐flour composites *

Effective interfacial adhesion between wood fibers and plastics is crucial for both the processing and ultimate performance of wood–plastic composites. Coupling agents are added to wood–plastic composites to promote adhesion between the hydrophilic wood surface and hydrophobic polymer matrix, but to date no coupling agent has been reported for PVC/wood‐fiber composites that significantly improved their performance and was also cost‐effective. This article presents the results of a study using chitin and chitosan, two natural polymers, as novel coupling agents for PVC/wood‐flour composites. Addition of chitin and chitosan coupling agents to PVC/wood‐flour composites increased their flexural strength by ～20%, their flexural modulus by ～16%, and their storage modulus by ～33–74% compared to PVC/wood‐flour composite without the coupling agent. Significant improvement in composite performance was attained with 0.5 wt% of chitosan and when 6.67 wt% of chitin was used. J. VINYL ADDIT. TECHNOL., 11:160–165, 2005. © 2005 Society of Plastics Engineers     

Flame retardancy,antifungal efficacies,and physical–mechanical properties for wood/polymer composites containing zinc borate

This work aimed to examine flame retardancy, antifungal performance and physical–mechanical properties for silane‐treated wood–polymer composites (WPCs) containing zinc borate (ZnB). ZnB with content from 0.0 to 7.0 wt% was added to WPCs, and silane‐treated wood contents were varied. The polymers used were poly(vinyl chloride) (PVC) and high‐density polyethylene (HDPE). The decay test was performed according to the European standard EN 113. Loweporus sp., a white‐rot fungus, was used for antifungal performance evaluation. Antifungal performance was observed to decrease with wood content. Incorporation of ZnB at 1.0 wt% significantly increased the antifungal performance of WPCs. ZnB content of greater than 1.0 wt% lowered the antifungal properties of WPCs. The results suggested that the wood/PVC composite exhibited better antifungal performance than the wood/HDPE composite. The addition of wood flour to PVC and HDPE decreased flame retardancy, whereas the incorporation of ZnB retained the flame retardancy. ZnB was found to be more appropriate for wood/PVC than wood/HDPE as a result of hydrogen chloride generated from the dehydrochlorination reaction of PVC. The results indicated that the addition of ZnB did not affect the physical‐mechanical properties of neat polymers and the composites. Copyright © 2016 John Wiley & Sons, Ltd.     

Moisture absorption effects on the thermal and mechanical properties of wood flour/linseed oil resin composites

The thermal and mechanical behavior of new natural polymeric composite materials after exposure to humid environments must be well known and understood in order to predict their performance in final applications. For this reason, composites made from unsaturated polyesters based on linseed oil and filled with wood flour were exposed to environments of different relative humidities and their final properties were measured. In general, the equilibrium moisture content increased as the wood flour percentage increased. Dynamic mechanical tests performed in temperature scan mode were carried out in order to monitor the changes resulting from moisture absorption on the main transition temperature of the matrix (T_α). The temperature of this transition decreased as the amount of absorbed water increased, but the effect was partially reversible by re‐drying the samples. The mechanical properties were also strongly affected by moisture. The flexural modulus and ultimate stress of the composites decreased after equilibration in humid environments. Copyright © 2006 Society of Chemical Industry     

Effects of wood flour and chitosan on mechanical,chemical, and thermal properties of polylactide

Composites of polylactide (PLA, 100–60 wt%) and wood flour (0–40 wt%) were prepared to assess the effects of wood filler content on the mechanical, chemical, thermal, and morphological properties of the composites. The polysaccharide chitosan (0–10 wt%) was added as a potential coupling agent for the PLA‐wood flour composites. Addition of wood flour significantly increased the flexural modulus and the storage modulus of PLA‐wood flour composite, but neither the wood flour nor chitosan had an effect on the glass transition temperature (T_g). Fourier transform infrared spectra did not show any evidence of covalent bonding, but chitosan at the interface between wood and PLA is thought to have formed hydrogen bonds to PLA‐carbonyl groups. SEM images of fracture surfaces showed that fiber breakage was far more common than fiber pullout in the composites. No evidence of discrete chitosan domains was seen in SEM micrographs. When added at up to 10 wt% (based on wood flour mass), chitosan showed no significant effect on the mechanical, chemical, or thermal properties of the composites, with property changes depending on wood flour content only. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers.     

Thermophysical properties of anhydride‐cured epoxy/nano‐clay composites

Polymer nano‐composites made with a matrix of anhydride‐cured diglycidyl ether of bisphenol A (DGEBA) and reinforced with organo‐montmorillonite clay were investigated. A sonication technique was used to process the epoxy/clay nano‐composites. The thermal properties of the nano‐composites were measured with dynamic mechanical analysis (DMA). The glass transition temperature T_g of the anhydride‐cured epoxy was higher than the room temperature (RT). For samples with 6.25 wt% (4.0 vol%) of clay, the storage modulus at 30°C and at (T_g + 15)°C was observed to increase 43% and 230%, respectively, relative to the value of unfilled epoxy. The clay reinforcing effect was evaluated using the Tandon‐Weng model for randomly oriented particulate filled composites. Transmission electron microscopy (TEM) examination of the nano‐composites prepared by sonication of clays in acetone showed well‐dispersed platelets in the nano‐composites. The clay nano‐platelets were observed to be well‐intercalated/expanded in the anhydride‐cured epoxy resin system. POLYM. COMPOS., 26:42–51, 2005. © 2004 Society of Plastics Engineers.     

Effect of Polyhedral Oligomeric Silsesquioxanes Nanoparticles on Thermal and Mechanical Properties of Poly(vinyl chloride) Composite Materials

The modification of poly(vinyl chloride) (PVC) by polyhedral silsesquioxane containing both methacryl and octyl groups (MeOctPOSS) was the task of studies. The PVC nanocomposites with MeOctPOSS concentration between 1 and 10 wt% were prepared by melt mixing processing, and the homogeneity of MeOctPOSS dispersion in the polymeric matrix was confirmed by scanning electron microscopy and energy dispersive spectroscopy observations. The influence of MeOctPOSS on glass transition temperature (T_g) determined by means of dynamic mechanical thermal analysis (DMTA) and differential scanning calorimetry (DSC) was observed, whereas, higher the measurement frequency, higher the glass transition temperature was noted. The MeOctPOSS concentration‐dependent PVC glass transition temperature was shifted from 73.8°C to about 68°C (? = 1 Hz) and from 76.5°C to 70.8°C (? = 10 Hz) for increasing additive content. Similar result of decreasing T_g value was observed by DSC method. An introduction of 10 wt% of MeOctPOSS into the PVC matrix results in a visible decrease of the maximum value of loss modulus (G′) of approximately 12% and 18% by 1 Hz and 10 Hz, respectively, as well as in a significant reduction of the static elastic modulus. It was stated that the polyhedral oligomeric silsesquioxanes with both methacryl and octyl groups may act as plasticizers of the PVC matrix. J. VINYL ADDIT. TECHNOL., 25:E48–E54, 2019. © 2018 Society of Plastics Engineers     

Characterization of PVC cable insulation materials and products obtained after removal of additives

Organic solvents cyclohexane, dichloromethane, hexane, and tetrahydrofuran were tested to separate the dioctylphthalate (DOP) as plasticizer from the poly(vinyl chloride) (PVC)‐based materials. It was found that the efficiency of ultrasound‐enhanced hexane extraction of the DOP from PVC is 70% and the efficiency of the separation of the DOP and other compounds from the PVC by dissolution in THF followed by subsequent precipitation was 98–99%. Differential scanning calorimetry (DSC) and thermogravimetry (TG) were used to characterize the thermal behavior of PVC materials before and after extraction of plasticizers. It was found that during heating in the range 20–800°C the total mass loss measured for the nontreated, extracted, and precipitated PVC samples was 71.6, 66.6, and 97%, respectively. In the temperature range 200–340°C, the release of DOP, HCl, and CO₂ was observed by simultaneous thermogravimetry (TG)/FTIR. The effect of plasticizers on thermal behavior of PVC‐based insulation material was characterized by DSC in the range ?40–140°C. It was found that, concerning the PVC cable insulation material before treatment, the value of the glass transition temperature (T_g) was 1.4°C, whereas for the PVC sample extracted by hexane, the value of T_g was 39.5°C and for the PVC dissolved in THF and subsequently precipitated, the value of T_g was 80.4°C. Moreover, the PVC samples after extraction of plasticizers, fillers, and other agents were tested to characterize their thermal degradation. The TG and FTIR results of chemically nontreated, extracted, and precipitated samples were compared. The release of DOP, HCl, CO₂, and benzene was studied during thermal degradation of the samples by FTIR. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 788–795, 2006     

Thermal and dynamic mechanical behavior of poly(vinyl chloride)/wood flour composites

Thermal and dynamic mechanical behaviors of wood plastic composites made of poly vinyl chloride (PVC) and surface treated, untreated wood flour were characterized by using differential scanning calorimetry and dynamic mechanical analysis. Glass transition temperature (T_g) of PVC was slightly increased by the addition of wood flour and by wood flour surface treatments. Heat capacity differences (ΔC_p) of composites before and after glass transition were markedly reduced. PVC/wood composites exhibited smaller tan δ peaks than PVC alone, suggesting that less energy was dissipated for coordinated movements and disentanglements of PVC polymer chains in the composites. The rubbery plateaus of storage modulus (E′) curves almost disappeared for PVC/wood composites in contrast to a well defined plateau range for pure PVC. It is proposed that wood flour particles act as “physical crosslinking points” or “pinning centers” inside the PVC matrix, resulting in the absence of the rubbery plateau and high E′ above T_g. The mobility of PVC chain segments were further retarded by the presence of surface modified wood flour. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Gas absorption with filled polymer systems

This paper deals with the gas absorption behavior of polymer systems. The emphasis is on the difference between filled and unfilled polymers to explain heterogeneous nucleation in filled polymers. A Foaming Process Simulator has been built to study the gas absorption. It consists of a test chamber that holds the polymer samples. The chamber can be pressurized with gas up to 5000 psi and heated up to 450°F. The gas pressure is monitored by a high‐accuracy pressure transducer and recorded by a data acquisition system. The amount of gas absorbed by a polymer is determined from the pressure change in the test chamber. A rotor applies shear to the polymer melt to investigate the shear effects. Two polymer systems were tested: HDPE with/without talc, and PVC with/without calcium carbonate. The fillers were well dispersed as verified with scanning electron microscope. The tests were done at the melt temperatures from 120°C to 177°C and a saturation pressure of about 18.9 MPa. It was found that the filled polymers absorb more gas compared to the unfilled ones. It is suggested that there is a certain amount of gas accumulated in the filler‐polymer interface. This accumulated gas helps to create cells during the foaming process.     

A novel method to prepare zinc hydroxystannate-coated inorganic fillers and its effect on the fire properties of PVC cable materials

Fire-retardant (FR) properties, including limiting oxygen index, peak rate of heat release, and smoke parameter have been measured and compared for unfilled and filled polyvinyl-chloride (PVC)-based cable formulations, containing 15 wt% amounts of uncoated and zinc-hydroxystannate (ZHS)-coated magnesium hydroxide (MH) and calcium carbonate (CaCO₃) fillers at the same addition level. Of the uncoated fillers, MH was more effective at lowering flammability than CaCO₃. When the ZHS coating was applied to MH and CaCO₃, CaCO₃ became the most effective additive at lowering PVC flammability and smoke output. POLYM. ENG. SCI., 47:1163–1169, 2007. © 2007 Society of Plastics Engineers