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Walnut cake has the potential for use in preparing wood adhesives because of its richness in protein and carbohydrate. In this work, walnut cakes were treated with sodium periodate or potassium permanganate and then were directly used as wood adhesives. Their bonding properties, curing performances, thermal properties, and chemical structures were compared. The results showed that: (1) The oxidation by KMnO4was nonselective. The reaction was very intense, accompanied by the great variability of oxidation degree and degradation degree, enormous viscosity of oxidation products, high coating difficulty, and low content of active aldehyde groups. (2) The oxidation by NaIO4 was selective; the reaction was mild and easy to control. More active aldehydes could be produced and the treatment was beneficial for constructing a spatial net structure of the adhesive. (3) Compared with oxidation of KMnO4, the walnut cake adhesive prepared by NaIO4 oxidation exhibited a more compact structure, a higher crosslinking degree, low curing temperature, and high thermal stability after curing; its bonding performances met the requirements for Class II plywood specified in GB/T 17657(2013). [ABSTRACT FROM AUTHOR]

Green composite materials are a means of reducing reliance on synthetic and especially single-use plastics (SUP) and raising public awareness of the need for urgent action to protect the planet. Natural (lignocellulosic) fibres are increasingly utilized as the reinforcement in polymer matrix composites, in search for increased renewability and sustainability. This work concerns the effect of washing ramie (Boehmeria nivea) fibres using sodium lauryl sulphate (SLS) surfactant. The SLS-treated ramie fibres were examined for their morphological, physical, thermal, structural, and mechanical properties by powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and tensile testing. SLS treated ramie fibres density and crystallinity index values were 1.23 g/cc and 84.5%, respectively, with a very high cellulose content of 81.3%, because hemicellulose and loose particles were dissolved. SEM images depicted the relevant changes, with no significant damage on treated fibre surfaces. With some assistance from the treatment, fibres initiated their degradation only above 250 °C, culminating at 327 °C, which appears suitable for the manufacturing of composites with the most common matrices.

The acoustic and thermal properties were determined for biodegradable insulation materials produced from desilicated wheat straws with two different fungi and three different incubation periods. Ganoderma lucidum (GL) and Pleurotus ostreatus (PO) fungi and wheat straw were exposed to fungal incubation for 10, 20, and 30 days to produce mycelium-based insulation materials. The sound absorption coefficients of mycelium-based insulation boards produced using PO fungus were higher than those produced with GL fungus. It was found that the acoustic absorption coefficients of insulation boards produced using PO fungus at 1,000 Hz were 87 to 99% according to the incubation periods. The sound transmission losses of mycelium-based insulation boards produced ranged from 46.4 to 59.7 dBa at 1000 Hz. The group of boards labeled as YP2 exhibited the lowest level of sound transmission loss, whereas GL2 revealed the highest degree of sound transmission loss at 1000 Hz. The lowest thermal conductivity coefficient was obtained in insulation boards produced with PO fungus and an incubation period of 20 days. The limiting oxygen index (LOI) value of mycelium-based insulation materials was considerably higher than the insulation boards commonly used today. Thermogravimetric analysis and derivative thermogravimetry curves of mycelium-based insulation materials were also determined.

The acoustic and thermal properties were determined for biodegradable insulation materials produced from desilicated wheat straws with two different fungi and three different incubation periods. Ganoderma lucidum (GL) and Pleurotus ostreatus (PO) fungi and wheat straw were exposed to fungal incubation for 10, 20, and 30 days to produce mycelium-based insulation materials. The sound absorption coefficients of mycelium-based insulation boards produced using PO fungus were higher than those produced with GL fungus. It was found that the acoustic absorption coefficients of insulation boards produced using PO fungus at 1,000 Hz were 87 to 99% according to the incubation periods. The sound transmission losses of mycelium-based insulation boards produced ranged from 46.4 to 59.7 dBa at 1000 Hz. The group of boards labeled as YP2 exhibited the lowest level of sound transmission loss, whereas GL2 revealed the highest degree of sound transmission loss at 1000 Hz. The lowest thermal conductivity coefficient was obtained in insulation boards produced with PO fungus and an incubation period of 20 days. The limiting oxygen index (LOI) value of mycelium-based insulation materials was considerably higher than the insulation boards commonly used today. Thermogravimetric analysis and derivative thermogravimetry curves of mycelium-based insulation materials were also determined. [ABSTRACT FROM AUTHOR]

Using phase change materials (PCMs) is an efficient solution for reducing energy consumption in buildings. These materials have a large capacity for storing thermal energy, making them an appealing option for energy management purposes. Phase change materials have been successfully incorporated into various construction materials such as concrete, brick, or plaster. The primary objective of this review is to examine previous studies conducted on the application of PCMs in wood. The initial section presents an overview of the direct impregnation techniques utilized for wooden materials. This is followed by a discussion on the implementation of macroencapsulated PCMs in wooden structures that are typically present in residential buildings. In addition, the use of shape-stabilized PCM/wood composites, preventing potential leaks during the phase change transition, is explored. Finally, patents related to the use of PCMs in wood are described. Future challenges include the incorporation of PCMs into wood composites to improve their thermal properties. This literature review shows that there is a gap in knowledge regarding the utilization of phase change materials in wood-based panels such as oriented strandboards, fiberboards, and particleboards. This provides an opportunity for future research to improve the performance of the products manufactured by the wood-based panels industry.

Mycelium from fungi can serve as the matrix or as a self-grown binder in a biocomposite. The reinforcing component may consist of various combinations of agro-based waste in short fiber or powder form. The complexity of their development is linked not only to the selection of the substrate, but also to the growth conditions of the mycelial material and its consolidation in a final form by the temperature increase that takes place. These materials have initially been proposed as a replacement for polystyrene foams, and the characterization is concentrated on compression performance and acoustic and thermal insulation properties. The present review concentrates on substrates that originated from the large productive system based on hemp (shives or hurds, waste fibers, and mats). Attention is paid to the performance obtained and to the amount of waste that is possibly employed to serve as the substrate. [ABSTRACT FROM AUTHOR]

Using phase change materials (PCMs) is an efficient solution for reducing energy consumption in buildings. These materials have a large capacity for storing thermal energy, making them an appealing option for energy management purposes. Phase change materials have been successfully incorporated into various construction materials such as concrete, brick, or plaster. The primary objective of this review is to examine previous studies conducted on the application of PCMs in wood. The initial section presents an overview of the direct impregnation techniques utilized for wooden materials. This is followed by a discussion on the implementation of macroencapsulated PCMs in wooden structures that are typically present in residential buildings. In addition, the use of shape-stabilized PCM/wood composites, preventing potential leaks during the phase change transition, is explored. Finally, patents related to the use of PCMs in wood are described. Future challenges include the incorporation of PCMs into wood composites to improve their thermal properties. This literature review shows that there is a gap in knowledge regarding the utilization of phase change materials in wood-based panels such as oriented strandboards, fiberboards, and particleboards. This provides an opportunity for future research to improve the performance of the products manufactured by the wood-based panels industry. [ABSTRACT FROM AUTHOR]

This study investigated the effects of Iroko wood flour (WF) and nanotitanium dioxide (TiO2) concentration on the properties of polypropylene (PP)-based composites, including accelerated weathering resistance, tribological behavior, thermal stability, physical characteristics, mechanical strength, morphological features, color changes, and surface roughness. The results showed that the presence of WF and TiO2 significantly influenced the density, hardness, thermal stability, crystallinity, coefficient of friction, and wear rate of the composites. Both fillers positively impacted the tensile strength, flexural strength, and flexural modulus of the composites, although the elongation at break values decreased. TiO2 addition enhanced thermal stability and protection against UV radiation, whereas using wood flour negatively affected color properties. Moreover, the surface roughness of the composites was affected by weathering time and wood flour content. These findings highlight the potential of WF and TiO2 as effective fillers for enhancing PPbased composites' properties and weathering resistance. [ABSTRACT FROM AUTHOR]

The effects of acidified chlorite (NaClO2) and totally chlorine free (TCF) bleaching were evaluated relative to the properties of microcrystalline cellulose (MCC) fabricated from oil palm empty fruit bunch fibres (OPEFB). The MCC properties were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA) methods, and they were compared with commercial MCC. The results revealed that all MCC belongs to cellulose type 1 and OPEFB-NaClO2-MCC showed a higher crystallinity index than OPEFB-TCF-MCC. The TGA indicated that all MCC samples showed a higher decomposition temperature compared to pure cellulose. However, OPEFB-NaClO2-MCC showed better thermal stability than OPEFB-TCF-MCC. It was clear from SEM images that the different MCC particles had rough surfaces and micro-sized particles. Overall, results confirmed that the obtained MCC samples displayed comparable properties with those of commercial MCC. The MCC produced from OPEFB using NaClO2 is a promising material to prepare high value-added products compared to MCC produced using TCF delignification treatment.

Chitosan foams with promising mechanical properties, heat-insulating ability, and flame retardancy were produced through oven drying. The chitosan foams were reinforced with cellulose, boric acid, and different ratios of activated carbon. The foams showed desirable low density (80.2 to 109.8 kg/m3) and compression properties. The compression resistance and compression modulus of foams ranged between 53.6 and 98.5 KPa and 214 to 394 KPa, respectively. Thermal conductivity tests revealed that the foams endowed low thermal conductivity values (0.035 to 0.051 W/mK). The limiting oxygen index (LOI) of the foams was as high as 32.9% for activated carbon (20 g/L). The activated carbon reinforcement produced higher thermal properties and decreased the mass loss 48.1% at 600 °C. The produced foams exhibited good biodegradability (39% degradation in 15 days). The overall test results showed that the chitosan foams can be utilized as a promising environmentally friendly material in thermal insulation fields.

Bioderived poly(lactic acid) (PLA) is a promising alternative for fossilbased polymers, but its poor hydrophilicity, high brittleness, and low heatresistance are problems for its utilization. In this work, bleached softwood kraft pulp (BSKP) fiber was adopted to modify PLA with MAPP as the coupling agent, with BSKP accounting for 10 wt% to 50 wt%. Internal mixing (IM) was applied to mix the PLA/fiber blend instead of screw grinding. The thermal and mechanical properties of the composites were assessed. The IM process was proven qualified for its effective dispersion of BSKP fibers in the PLA matrix. At a fiber loading of 50 wt%, IMprocessed composites acquired satisfactory tensile strength (50.49 MPa, slightly higher than PLA) and Young's modulus (2.56 GPa, 45.8% higher than PLA). The pulp fillers matched PLA matrix well for the characteristic temperatures in thermal decomposition. The BSKP/PLA composites were thermally strengthened by pulp fibers characterized by higher content of residues. The fibers improved the interfacial crystallinity of PLA in the composites (i.e., from 5.22% to 11.86%). The increased crystallinity resulted in enhanced stiffness or weaker damping performance of the composites. In conclusion, natural plant fibers are a feasible option to modify PLA for extended applications. [ABSTRACT FROM AUTHOR]

This study investigated the tensile properties and thermal behavior of virgin and hot press molded HDPE composites filled with different particle size and content of used beverage cartons which were the Tetra Pak® cartons. The mechanical properties of the composites were positively influenced by particle size of the used beverage carton, such that the smallest particle size gave the highest tensile strength and tensile modulus. The tensile strength of the specimens decreased with increasing filler content (40 to 70 wt%), while the tensile modulus rose. Furthermore, the filler size and its content affected the thermal behavior of the specimens. Calorimetry analysis of composite specimens showed that melting temperature and enthalpy values of virgin HDPE and recycled-HDPE decreased with increasing Tetra Pak® content. In all composite groups produced by adding Tetra Pak®, the degree of crystallinity decreased as a function of Tetra Pak® addition compared to the pure HDPE. Increasing particle size adversely affected the crystallization degree, which decreased with increasing particle size while the HDPE maintained its crystalline form. As for the recycled-HDPE composites, the degree of crystallization was reduced by increasing the Tetra Pak® content, but this was still noticeably higher than that of the HDPE. [ABSTRACT FROM AUTHOR]

The effects of acidified chlorite (NaClO2) and totally chlorine free (TCF) bleaching were evaluated relative to the properties of microcrystalline cellulose (MCC) fabricated from oil palm empty fruit bunch fibres (OPEFB). The MCC properties were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA) methods, and they were compared with commercial MCC. The results revealed that all MCC belongs to cellulose type 1 and OPEFBNaClO2-MCC showed a higher crystallinity index than OPEFB-TCF-MCC. The TGA indicated that all MCC samples showed a higher decomposition temperature compared to pure cellulose. However, OPEFB-NaClO2-MCC showed better thermal stability than OPEFB-TCF-MCC. It was clear from SEM images that the different MCC particles had rough surfaces and micro-sized particles. Overall, results confirmed that the obtained MCC samples displayed comparable properties with those of commercial MCC. The MCC produced from OPEFB using NaClO2 is a promising material to prepare high value-added products compared to MCC produced using TCF delignification treatment. [ABSTRACT FROM AUTHOR]

Wood plastic composites (WPCs) were prepared by extrusion molding with eucalyptus powder, polyvinyl chloride (PVC), and silica as additives. The mechanical properties, creep behavior, thermal properties, and crosssection microstructure of the composites were analyzed by universal testing machine, thermogravimetric analyzer, and scanning electron microscope. The results show that with the increase of silica content, the tensile strength, bending strength, and impact strength of the WPCs first increased and then decreased. When the silica content was 3.0%, the tensile strength, bending strength, and impact strength of WPC reached the maximum values of 27.5 MPa, 48.8 MPa, and 4.18 KJ · m-2, respectively, which represented increases of 12.6%, 9.4%, and 20.1%, respectively, compared with those without silica. When the stress was 13.4 MPa, the strain value of 3.0% SiO2-eucalyptus/PVC wood plastic composite was 3.3 times that of 4.46 MPa and 1.7 times that of 8.92 MPa. The pyrolysis process of eucalyptus/PVC WPCs showed a similar trend with different silica content. [ABSTRACT FROM AUTHOR]

Chitosan foams with promising mechanical properties, heat-insulating ability, and flame retardancy were produced through oven drying. The chitosan foams were reinforced with cellulose, boric acid, and different ratios of activated carbon. The foams showed desirable low density (80.2 to 109.8 kg/m³) and compression properties. The compression resistance and compression modulus of foams ranged between 53.6 and 98.5 KPa and 214 to 394 KPa, respectively. Thermal conductivity tests revealed that the foams endowed low thermal conductivity values (0.035 to 0.051 W/mK). The limiting oxygen index (LOI) of the foams was as high as 32.9% for activated carbon (20 g/L). The activated carbon reinforcement produced higher thermal properties and decreased the mass loss 48.1% at 600 °C. The produced foams exhibited good biodegradability (39% degradation in 15 days). The overall test results showed that the chitosan foams can be utilized as a promising environmentally friendly material in thermal insulation fields. [ABSTRACT FROM AUTHOR]

The isolation of cellulosic fibers and their applications in composite materials have drawn considerable interest due to their outstanding thermal and mechanical properties combined with light-weight character, biodegradability, and renewability. Bamboo is a fast-growing plant, and its properties include sustainability and excellent tensile strength. In this study, bamboo fibers from the culms and shoots of Dendrocalamus asper were treated with 5 wt% sodium hydroxide and subjected to ultrasonication for 5 hours to obtain bamboo cellulose. Infra-red spectra showed that lignin and hemicelluloses were removed after treatment. With the removal of amorphous cellulosic regions, both cellulosic fibers exhibited higher decomposition temperatures than the raw fibers. Thermogravimetric analysis confirmed that both types of bamboo cellulose had a peak decomposition temperature at 408 °C. Cellulose isolated from the bamboo shoots exhibited similar chemical and thermal properties, indicating its huge potential as an alternative to mature bamboo culms. [ABSTRACT FROM AUTHOR]

Chemical, physical, thermal properties and bonding quality of phenolformaldehyde resol resin (PF) synthesized with single-walled carbon nanotubes (SWCNTs) was evaluated at varying ratios from 1 wt% to 5 wt%. The effect of the SWCNTs addition on thermal and chemical properties of the PF resins was characterized by thermal gravimetric analysis (TGA) and Fourier transform infrared (FT-IR) spectroscopy, respectively. FT-IR analysis revealed that the peaks of the modified PF resol resins were similar to those of the reference (laboratory-produced) PF resol resin. These similarities indicated that the synthesis of the resins with phenol, formaldehyde, and carbon nano tubes was successful. The PF resins modified using SWCNTs demonstrated higher thermal stability than the reference PF resin. It was found that the bonding strength of the PF resin containing 3 wt% SWCNTs could reach 12.45 N/mm2 in dry conditions and 7.57 N/mm2 in wet conditions. The bonding test results demonstrated that the SWCNTs were able to improve the bonding performance of the resin under dry and/or wet conditions. This work presents an effective method to improve PF resins with SWCNTs reinforcement for use in the wood and/or polymer composite industries. [ABSTRACT FROM AUTHOR]

Biomass densification, which is also known as briquetting of sawdust and other agro residues, has been practiced for many years in several countries. The purpose of the present study was to produce fuel briquettes using heat-dried bagasse and to improve their physical properties and thermal value through using varying proportions of bagasse powder as the filler material and lignin as the natural binder. The results showed that lignin had a significant desirable effect on the entire properties of the prepared briquettes. In contrast, as a cellulose-based filler, bagasse powder was also able to significantly improve the thermal energy of the briquettes through increasing the briquettes’ density and mitigating porosity and moisture content. On this basis, according to the obtained results it can be stated that the process of heat-drying, using lignin as the binding element, and using cellulose-based powders, such as bagasse, as the filler are all suitable alternatives to increase the energy yielded by briquettes biomasses. [ABSTRACT FROM AUTHOR]

This study investigated the effects of the pressing temperature on the mechanical and physical properties of binderless bark particleboard made from Gelam bark waste and the improvement of those properties. In addition, the thermal insulation properties of the particleboard were determined. Four different temperatures (140 °C, 160 °C, 180 °C, and 200 °C) were used to make single-layer binderless bark particleboard with a target density of less than or equal to 0.59 g/cm3. Results revealed that the pressing temperature affected the mechanical properties (modulus of rupture, modulus of elasticity, and tensile strength perpendicular to panel surface), which increased as the temperature increased, and the physical properties (thickness swelling and water absorption), which decreased as the temperature increased. Based on the Tukey test, increasing the temperature from 180 to 200 °C did not significantly affect the mechanical or physical properties, except for the tensile strength perpendicular to panel surface. None of the mechanical properties met SNI standard 03-2105-2006 (2006); however, the 12% maximum thickness swelling requirement was met for binderless bark particleboard hot-pressed at 200 °C. Binderless bark particleboard hot-pressed at 200 °C had high water resistance, regardless of its low strength, and a thermal conductivity value of 0.14 W/m·K. [ABSTRACT FROM AUTHOR]

The morphological and thermal properties of composites containing a bioplastic blend and micro/nano-sized biochar from pyrolyzed jatropha seeds from microwave pyrolyzed jatropha seeds were investigated using scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, and differential scanning calorimetry. The biocomposite samples exhibited a brittle structure with a slightly ductile chip-like appearance. The Fourier transform infrared spectroscopy results for the PLA/PEMA/BC bio-composites were comparable to the PLA/BC biocomposites. A lower bio-filler content had more pronounced peak intensities than the higher bio-filler content biocomposites. The added PEMA compatibilizer in the PLA/PEMA/BC biocomposite showed more pronounced peaks, which indicated slightly improved bonding/interaction between the bio-filler and the matrix. Overall, increasing bio-filler content did not drastically affect the functional groups of the biocomposites. Thermogravimetric and differential scanning calorimetry analysis showed the developed biocomposites had a slight improvement in thermal stability, in comparison to the PLA sample. Improvements in the thermal stability of the PLA/PEMA/BC biocomposite could be attributed to the additional hydroxyl group, which was due to the added PEMA in the PLA and PLA/BC. According to the results of the analysis of the developed biocomposites, the biocomposites were more brittle and had reasonable thermal stability. [ABSTRACT FROM AUTHOR]

The thermal properties of wood-plastic composites (WPCs) and typical heating floor substrates heated by an electrothermal film were studied. Their effects on human feelings and the human autonomic nerve system were also investigated. The temperature changes of the specimens during heating and cooling were analyzed with an infrared thermal imager. People's subjective feelings of touching different materials were analyzed with a semantic differential (SD) technique, and their electrocardiography was recorded with a multi-channel physiological signal acquisition system. The thermal conductivity, temperature variation, tactile impression, and heart rate variability of WPCs and other heating floor substrates were investigated. The WPCs presented a markedly lower thermal conductivity and superior tactile impression compared with ceramic tile, which has a similar density to WPCs. There was a negative correlation between the scores of the warm-cool feeling and the density of the heating floor substrates under room temperature (19 °C ± 1 °C), and a positive correlation when heated (33 °C ± 1 °C). The thermal conductivity and heat storage capacity of WPC were higher than those of solid wood. Electric heating composite floors with a high comfort level and good thermal properties could be manufactured by combining WPCs and solid wood.

Sugar palm fibre (SPF) was used to prepare composites with phenolic resin. The SPF underwent treatment with either sea water for 30 d or a 0.5% alkaline solution for 4 h. The composites contained 30% (vol.) SPF in a powdered form, and the composite samples were fabricated by a hot press machine. The effects of the fibre treatments on the mechanical (flexural, impact, and compressive), thermal, and morphological properties of the composites were analyzed. The SPF treatments considerably improved the mechanical properties of the composites compared with the untreated composite. The alkaline treatment resulted in the most improved flexural and impact strength of the composites. In contrast, the sea water treatment had the best results for improving the compressive strength. Morphological analyses indicated that the surface treatments improved the fibre-matrix bonding. The thermal degradation analysis showed that both the sea water and alkaline treatments of the SPF slightly affected the thermal stability of the composites. Consequently, SPF can be effectively used as an alternative natural fibre for reinforcing bio-composites.

Bacterial cellulose nanofibers (BCNF), obtained by the mechanical disintegration of BC pellicles, were used without any surface treatment for the fabrication of poly(lactic acid) (PLA) nanocomposites by a melt compounding process. The addition of BCNF in different amounts improved both the Young’s modulus and tensile strength of PLA. A 22% increase in these properties was observed in the nanocomposite with 2 wt.% nanofibers, due to the BCNF network formed at this concentration and characterized by atomic force microscopy. BCNF addition also increased the crystallinity and thermal stability of PLA, which were evaluated by thermal analysis. Due to the high purity of BCNF and the environmental friendliness of melt processing, it was concluded that PLA/BCNF nanocomposites can be designed for biomedical field and food packaging.

The influence of repeated cycles of injection molding on some mechanical and thermal properties of wood plastic composites (WPCs) was investigated. Pine wood flour (50 wt%) was mixed with HDPE (50 wt%) containing compatibilizing agent (MAPE, 3 wt%) in a co-rotating twin-screw extruder. The test specimens were produced by injection molding from the pellets dried to the moisture content (MC) of 1%. After the mechanical properties of the WPC test specimens were determined, the failed specimens were subsequently pelletized. These pellets were stored and dried for 4 to 6 h until the repeated injection was molded. These processes were repeated seven times. The results revealed that the flexural strength of WPCs increased by about 5.26% from the original granules to the third injection cycle, but further increments in the number of cycles decreased the flexural strength. The tensile strength and tensile modulus of the WPC specimens increased until the third cycle of injection molding while they tended to decrease after the third injection cycle.

Roselle (Hibiscus sabdariffa L.) bast fibre reinforced vinyl ester (VE) was prepared using a hand lay-up method and an internal mixer. The composite samples were prepared under two different parameters: with various fibre contents; and without fibre (neat VE). The mechanical properties (tensile and impact strength) and thermal properties were investigated. The morphological properties of impact fracture samples were studied using a scanning electron microscope (SEM). Roselle fibre reinforced VE (RFVE) composites showed increased tensile strength and tensile modulus. The highest tensile strength and modulus were at 20vt% fibre loading. However, impact strength decreased as the fibre loading increased. SEM showed that there was good fibre/matrix adhesion and fibre dispersion for 20% fibre loading, which was reflected in the good tensile strength properties. However, fibre agglomeration was seen at higher fibre loads. The results from thermogravimetric analysis (TGA) and derivative thermogravimetric analysis (DTG) showed three major degradations of the RFVE, which were the loss of moisture content, degradation of hemicelluloses, and degradation of cellulose. The thermal analysis showed enhancements in the residual content of the composite materials, thereby improving the thermal stability. However, there was no major difference seen in the degradation temperature.

Global energy consumption is expected to grow by 56% between 2010 and 2040. Renewable energy is one of the fastest-growing energy resources, and biomass is a major feedstock for providing renewable energy. It constitutes up to 35% of the main energy consumption in developing countries. Densified solid biofuel with high density gets a lot of attention due to its uniform shape and low heating cost. When considering densified solid biofuels as a viable solution for energy production, its quality needs to be improved. Solid biofuel quality is a function of the chemical composition and physical properties of the raw materials. It is widely reported that the raw material chemical composition has a major effect on the final solid biofuel quality, as it influences the heating value, ash content, and mechanical durability. The moisture content influences the net heating value, combustion efficiency, and mechanical durability of solid biofuels. The bulk density influences the mechanical durability, thermal characteristics, as well as handling and storage costs of solid biofuels. This work reviewed the latest developments on the effects of the chemical composition, moisture content, and bulk density of raw materials on the thermal efficiency, emission, and mechanical durability of densified solid biofuels. [ABSTRACT FROM AUTHOR]

Microcellulose has shown advantageous character as a reinforcement in polymeric materials and produces relatively light compounds with high specific properties. This research aimed to obtain microcellulose (crystals and fibers) from the macrophyte Typha domingensis for use as a polypropylene reinforcement material for impact strength improvement and to use stearic acid as an interfacial modifier (surfactant) between the polypropylene and cellulosic materials. A commercial cellulose was used to compare the effectiveness of the microcellulose isolated from the macrophyte. The results demonstrated the procedures were efficient at obtaining microcellulose. The analysis of the chemical composition indicated an increase in the α-cellulose content from 63.2% in the raw material to 97.9% in the bleached cellulose. The X-ray diffraction patterns showed that the chemical treatments changed the crystallinity. The thermogravimetric analysis revealed an increase in the thermal stability of the bleached cellulose compared with that of the raw material. The thermal stability of the macrophyte was higher than that of commercial cellulose. The scanning electron micrographs revealed the presence of longitudinal slits that favored interactions with the polymer matrix. The impact strength was greatly improved for the composites compared with the pure polypropylene. [ABSTRACT FROM AUTHOR]

Sugar palm fibers (SPF) reinforced vinyl ester (VE) composites were prepared in this study. The SPFs were obtained from three different geographical locations: Kuala Jempol (Peninsular Malaysia), Tawau (West Malaysia), and Tasik Malaya (Indonesia). The SPFs were utilized as reinforcement material with a fixed loading of 10 wt.%. The reinforced VE composites were prepared using a wet lay-up compression moulding method. The physical properties examined were water absorption, thickness swelling, and moisture content. To determine the strength of the SPF composites, tests on the tensile, flexural, and impact strength related to mechanical properties were completed. A thermogravimetric analysis (TGA) was completed to observe the thermal properties. This study confirmed that the properties of the composites were affected by the strength of the fiber. The SPF/VE composites obtained from Kuala Jempol had the highest tensile, flexural, and impact strength compared to the SPF/VE composites from Indonesia and Tawua. In addition, SPF Jempol/VE also recorded the highest percentage of water absorption, thickness swelling, and moisture content. A comparison of thermal properties showed that SPF Tawau/VE had highest percentage of mass loss between fibers from the three geographic locations. [ABSTRACT FROM AUTHOR]

The catalytic acetylation of bamboo (Phyllostachys pubescens) was compared with acetylation using concentrated sulfuric acid, acetic acid, potassium acetate, and noncatalytic acetylation at 120 °C for 3 h. The weight percentage gain, dimensional stability, color difference, and wettability of bamboo after the acetylation was comprehensively measured. Also, the chemical and thermal properties of the resultant bamboo were characterized by Fourier transform infrared spectroscopy (FTIR) and thermogravimetric (TG) analysis. The results showed that the potassium acetate-catalyzed acetylation of bamboo greatly accelerated the reaction degree, had little effect on color change, extraordinarily decreased wettability, and had little irregular impact on the dimensional stability. The catalytic activity was followed by potassium acetate, sulfuric acid, noncatalytic acid, and acetic acid. The FTIR analysis showed that the functional groups in the acetylated bamboo were mainly affected by different catalysts. The thermal stability of acetylated bamboo was higher than the untreated bamboo. In particular, potassium acetate-catalytic acetylation greatly reacted with -OH groups and increased thermal decomposition. [ABSTRACT FROM AUTHOR]

The depletion of fossil resources and the environmental impact of petroleum-based plastic materials have driven a strong global interest in renewable biobased polymers and composites derived from natural resources. Since biodegradable polymers have their own drawbacks, it is often combined as a composite with other fillers. Polypropylene (PP)/Poly(3-hydroxybutyrate) (PHB) composite films and lignocresol (LC)/PP/PHB composite films were cast by blending methods. This study investigated the effects of the amounts of added PP fiber and LC on the mechanical and thermal properties in the corresponding composite films. The overall properties of LC/PP/PHB composite films were best with 8 wt.% PP fiber content and 3 wt.% LC content. The tensile strength (13.00 MPa) was up to 1.25 times that of the original PHB film (10.44 MPa), and the thermal properties of the composite films were improved by adding 3 wt.% LC. Thermogravimetry (TG) analysis indicated that the onset temperature (382.0 °C) rose by 50.7 °C compared with PP/PHB film (331.3 °C), and the residual mass was close to 0%.

This study reports the thermal characteristics of windows installed in the roof cladding of a block of flats in the second temperature zone of the Czech Republic, with boundary conditions for the design value θse = - 15 °C, according to the national standard ČSN 73 0540-3 (2005). The thermal behaviour of these elements was evaluated with regard to the condensation on roof windows, with four different types of spacer frames and the given boundary conditions, for maintenance of the thermal and technical humidity comfort of the interior. The tests of the surface temperatures of the diagnosed glazed roof units at the glazing of the wooden windows demonstrated that the SGG composite spacer was the best from a thermal perspective. The spacer frames based on aluminum, stainless steel, and a combination of stainless steel and plastic (TGI) did not provide adequate thermal insulation characteristics for usage in roof windows under the given climatic conditions, and condensation occurred on the glass surfaces.

Pinus pinaster wood was pulped in ethanol/water medium catalyzed with sulfuric acid, and lignin was recovered from the liquid phase by precipitation upon water addition. Lignin samples were characterized for composition and thermal properties. Lignin samples were reacted with selected esterification agents (butyric, isobutyric, or crotonic anhydrides) under experimental conditions leading to extensive conversion of the available hydroxyl groups, and the esterified lignins were assessed for composition and thermal properties. Samples made up of crude polylactic acid or its blends with lignins (raw or esterified) were assayed for mechanical properties. The blends of polylactic acid with lignin modified with butyric anhydride presented higher Young’s modulus and elongation at break than neat polylactic acid.

To illustrate the effects of nano-bamboo charcoal (NBC) on the properties of bamboo plastic composites (BPC), nano-bamboo charcoal-bamboo plastic composites (NBC-BPC) were prepared at 0%, 2.5%, 5%, 7.5%, 10%, and 12.5% (w/v) NBC and characterized. The effects of NBC on the water absorption, fractured surfaces, mechanical properties, and thermal properties of the composites were investigated. NBC had strong interfacial interaction in the BPC, which greatly improved the interfacial adhesion of bamboo flour (BF) and high-density polyethylene (HDPE). The water resistance, flexural strengths, and tensile strengths of the composites were enhanced compared with traditional BPC when the volume of NBC reached a specific loading. These results demonstrated that the incorporation of NBC slightly improved the thermal properties of the synthesized composites.

The properties of poly(lactic acid) (PLA) bio-composite films reinforced with oil palm empty fruit bunch (OPEFB) fiber and nanosilica were studied in this work. The composite films were prepared via the solvent casting method. The composites were characterized via Fourier transform infrared spectroscopy (FTIR), UV-visible spectroscopy, field-emission scanning electron microscopy (FESEM), tensile testing, and X-ray diffraction (XRD). Ultraviolet visible spectroscopy results revealed that the PLA-based composites and neat PLA had similar light transmittances of approximately 89%. The FTIR and FESEM results showed that OPEFB fibers and nanosilica were embedded into the PLA matrix. The tensile strength of the composites with addition of nanosilica increased with an increasing fiber load content. The XRD analysis showed that the addition of organic or inorganic silica reduced the crystallinity of the composites. The water vapor permeability test results indicated that the inorganic silica decreased the diffusion rate of water molecules through the polymer film. The OPEFB-reinforced PLA blend with additional organic silica exhibited a higher thermal stability than the composites reinforced with inorganic silica.

High-temperature thermomechanical pulps (HT-TMP, defibrated at 150 to 170 °C) were compared to a reference TMP (defibrated at 130 °C) as a reinforcement for polylactic acid (PLA). Composites were prepared by melt compounding, followed by injection molding, gradually increasing the used fiber content from 0 to 20 wt.%. The injection-molded specimens were characterized by tensile and impact strength tests, scanning electron microscopy, water absorption tests, and differential scanning calorimetry. The TMP fiber damage was also characterized before and after melt compounding by optical analysis. At 20% fiber content, the Young’s modulus increased significantly, while the tensile strength remained unchanged and the impact strength decreased slightly. All fibers suffered damage during melt compounding, but the tensile strength remained about the same as in pure PLA. All types of TMP were able to increase the PLA rate of crystallization. The HT-TMP fibers were dispersed more evenly in PLA than the 130 °C TMP. The 170 °C TMP produced composites of lower water absorption than the other two TMP types, probably because of its lower hemicellulose content and its higher surface coverage by lignin.

To investigate epoxidized palm oil’s (EPO) potential as plasticizer for poly(lactic acid) (PLA), its plasticizing effect was compared with commercialized epoxidized soybean oil (ESO). The plasticizers were respectively melt-compounded into PLA at 3, 5, 10, and 15 wt.%. As it was aimed for the blends to be characterized towards packaging appropriate for food products, they were hot-pressed into ~0.3-mm sheets, which is the approximate thickness of clamshell packaging. Fourier transform infrared spectroscopy (FTIR) confirmed the plasticizers’ compatibility with PLA. At similar loadings, EPO was superior in reinforcing elongation at break (EAB), thermal, and barrier properties of PLA. The ductility of PLA was notably improved to 50.0% with addition of 3 wt.% of EPO. From thermogravimetric analysis (TGA), PLA/EPO5 improved PLA’s thermal stability, while all PLA/ESO blends reported reduced thermal stability. From differential scanning calorimetry (DSC), the increase in crystallinity and the shifts in enthalpy of fusions in all plasticized blends denoted facilitation of PLA to form thermally stable α-form crystals. The addition of EPO enabled PLA to become highly impermeable to oxygen, which can extend its potential in packaging extensive range of oxygen sensitive food.

Bamboo, among other natural plants, has a special structure, with different characterization along the culms and between species. In this study, the thermal stabilities of four bamboo species, named Dendrocalamus pendulus (DP), Dendrocalamus asper (DA), Gigantochloa levis (GL), and Gigantochloa scortechinii (GS), were investigated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) under a nitrogen atmosphere. Each species was divided into three different portions: bottom, middle, and top, and fibres were manually extracted from the specified sections of each species. The thermal analysis of extracted bamboo fibres indicated that the thermal degradation behaviour of each bamboo species varied from bottom to top and between species. However, these variations were lower in DA species compared to GS, GL, and DP, because of minor differences between lignocellulosic components of its three portions. The top and middle portions of the four species degraded at a higher temperature range (314 to 379 °C) than the bottom portions. The results of this study suggest that DA and GS species, according to their thermal stabilities, are most suitable for use as reinforcement in composite materials.

In the present study, oil palm empty fruit bunch (OPEFB) fibers were taken from a 25-year-old oil palm tree. The cellulosic nanofiber (CNF) was isolated from the OPEFB using a chemo-mechanical process and utilized as reinforcement in an epoxy matrix. Various CNF loading percentages (0 to 0.75%) were applied in the epoxy matrix to explore the potential of using OPEFB-CNF as reinforcement. The morphological, mechanical, physical, and thermal characteristics of the OPEFB nanofiber-reinforced epoxy composites were evaluated. Results showed that the 0.25% and 0.5% CNF loadings were homogenously distributed and well-dispersed in the composite matrix. Conversely, agglomeration was detected in the matrix with 0.75% CNF loading. Determination of the water absorption behavior of CNF-reinforced epoxy composites at various loadings revealed that the physical properties of the composites increased with reinforcement loading. Furthermore, the analyses of the mechanical and thermal properties of the CNF-reinforced composites revealed that the incorporation of OPEFB-CNF enhanced the mechanical performance and thermal stability up to 0.5% loading.

This study investigates methods for improving the heat resistance of polyvinyl alcohol/alkali lignin foam material (PLFM). Tetraethoxysilane (TEOS) was used as a precursor to prepare PLCFM by a sol-gel method. The PLCFM, prepared with different levels of TEOS, was characterized by Fourier Transform Infrared spectrometry (FTIR), Differential Scanning Calorimetry (DSC), and Thermogravimetric Analysis (TGA). The results indicated that the addition of silica notably improved the heat resistance properties and the initial decomposition temperature of the foam and exhibited good biocompatibility with the polyvinyl alcohol (PVOH) and alkali lignin. The melting temperature of the PLCFM also increased significantly. It reached 268 °C when the silica content was 10%, which was 110 °C higher than that of PLFM. The mechanical properties were also improved to 27.42 MPa.

Bleached bamboo fiber was treated with a high pressure enzymatic hydrolysis (HPEH) process in order to produce microfibrillated bamboo fiber (MBF). Mixture design of experiments was utilized to determine the optimal constituents of fiber, enzymes, and water for the HPEH process on the isolation yield of the MBF. Results showed the optimal combination for the maximal yield isolation of the MBF was 1 g fiber, 1 g enzyme, and 1 L water at 90 MPa and 70 °C. The influence of the reaction time of the HPEH process (6 to 48 h) was also evaluated in this study. Morphological and thermal property analyses of untreated and treated bamboo fibers revealed that the HPEH process was effective for removing non-cellulosic components from the fibers. Thus, the HPEH process is an effective method for the isolation of the MBF, with the benefits of elevated crystallinity and thermal stability.

The possibilities of utilizing an abundantly available agricultural waste, oil palm empty fruit bunch (OPEFB) fibers, for the development of nano-filler was investigated. The aim was to develop fire retardant nano-fillers from OPEFB fiber through grinding, chemical treatment (bromine water and SnCl2), and cryogenic crushing, followed by a high energy ball milling process. The structural, morphological, and thermal properties of nano-fillers were investigated by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The analysis revealed that the particle size distribution was reduced from micro to nano size in the range of around 14 to 100 nm. Scanning electron microscopy (SEM) observations revealed that the nanoparticles of OPEFB had irregular shapes. The elemental composition of the OPEFB were investigated by elemental dispersive X- ray analysis (EDX), showing the presence of tin, carbon, oxygen, chlorine, and bromine elements both before and after ball milling. Further, thermo-gravimetric analysis (TGA) and differential scanning calorimetry (DSC) indicated that the developed nanofillers exhibited enhanced thermal properties compared to the untreated fibers. Such results suggest that the developed nano-filler can be used for the fabrication of nanocomposites with improved fire retardancy.

The purpose of this study was to investigate the effect of white mud (WM) on mechanical and thermal properties of bamboo plastic composites (BPCs). Bamboo residue fibers (BRFs) and WM were added as the reinforcement, and high-density polyethylene (HDPE) served as the matrix. The lubricating agent and coupling agent were polyethylene wax and maleated polyethylene (MAPE), respectively. The mixture was used to manufacture BPCs using a twin-screw extruder. The crystal structure and thermal properties of BPCs were investigated by X-ray diffraction (XRD), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results showed that the particle size of the WM was 700 nm to 50 μm, which are made mainly of calcium carbonate. BPCs with WM significantly increased the flexural and tensile properties, but the impact strength decreased because of the presence of WM. The flexural and tensile strength of composites with 18 wt% BPF were increased by 36.81% and 6.26%, respectively, while the flexural and tensile modulus were increased by 164.29% and 64.33%, respectively. XRD demonstrated the WM had little effect on the crystal structure of BPCs. Compared to BPCs without WM, the T5% of composites with 22 wt% WM decreased by 27.9 °C. As the WM content increased, the crystallinity of the BPCs decreased initially, then increased with increasing WM content.

In this study, banana petiole-based cellulose nanofibril (CNF) films treated with graphene oxide (GO) were prepared and evaluated by means of Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), dynamic mechanical analysis (DMA), and thermogravimetric analysis (TGA). Tensile strengths (TS), dynamic mechanical properties, and thermal stabilities of the films were affected positively when the GO loading was less than 4.4 wt%. From these results, FTIR spectra, and SEM analyses, a strong coupling between the GO and the cellulose matrix could be concluded at lower GO loadings. The TGA and DMA results also suggested that the CNF film treated with 4.4 wt% GO had more char residue, better thermal stability, higher storage modulus, and higher retention ratio when compared to that without treatment. This work provides a new approach for more effective utilization of banana petiole as a feedstock for CNF and GO/CNF composites.

Hemp fiber-reinforced unsaturated polyester (UPE) composites were prepared by hand lay-up compression molding. The UPE resins were modified with butyl methacrylate (BMA) to improve the flexibility and toughness of the hemp-UPE composites. The results indicate that the toughness of the composites significantly increased as BMA usage increased. Compared to the unmodified UPE composites, the composites obtained from BMA-modified UPE resins had 27.4, 63.0, and 36.6% greater elongation at break, flexural strain, and impact strength, respectively. The optimum BMA usage to achieve an adequate balance of stiffness and toughness is 20 to 30%. Dynamic mechanical analysis (DMA) indicated that incorporation of BMA significantly decreased the storage modulus and glass transition temperature of the composites and increased its damping parameter due to the introduction of flexible segments into the UPE resins. Thermogravimetric analysis showed that the thermal stability of the composites decreased slightly following the incorporation of BMA. Scanning electron microscopy images of the impact-fractured surfaces of the composites revealed that BMA incorporation improved interfacial adhesion between hemp fibers and UPE matrices and that the main mechanism for the increase in the toughness of the composites was the added ductility of the matrices.

A major drawback of natural-based composites is the incorporation of reinforcements that are less thermally stable than the matrix; therefore, the thermal properties of the resultant composite material needs to be studied. In this work, orange wood fibers were used to reinforce polypropylene. The effects on the thermal properties of the polymeric matrix were analyzed. To this end, differential scanning calorimetry (DSC), thermogravimetry (TGA), thermomechanical analysis (TMA), and dynamic-mechanical analysis (DMA) were performed. It was found that the degradation of the material took place in two distinct phases: the reinforcement, close to 250 °C, and the matrix, above 340 °C. DSC results showed that fiber reinforcement did not influence the transition temperatures of the materials, although it did affect the polymer crystallinity value, increasing by 7% when the composite is reinforced with 50% of the lignocellulosic reinforcement. The coefficient of expansion obtained by TMA indicated that thermal expansion decreased as the amount of reinforcement increased. DMA assays showed that the reinforcement did not modify the glass transition (20 to 25 °C) temperature and confirmed that the addition of reinforcement increased the crystallinity of the product.

Roselle fibre is a type of natural fibre that can be utilized as a potential reinforcement filler in polymer composites for different applications. This work investigates the chemical, physical, mechanical, morphological, and thermal characteristics of roselle fibre at different levels of maturity (3, 6, and 9 months). The diameter of roselle fibre increases as the plant matures. However in contrast to this, the moisture content and water absorption of roselle fibre decrease as the plant matures. Chemical content of roselle fibres from plants of different ages indicate that as the plant matures, the cellulose content decreases. Tensile strength of roselle fibre decreases from 3 months old to 9 months old. The cross section of roselle fibre shows a typical morphology of bast fibre, where there is a lumen in the central of fibre.Thermal analysis results show that the effect of thermal decomposition of roselle fiber is almost the same for all plant ages. It is concluded that roselle fibres can be used as reinforced material for manufacturing of polymer composites. Based on its excellent properties, roselle fibres are suitable for different applications such as automotive and building components at lower cost.

Bamboo fiber was treated using a high-pressure enzyme hydrolysis process. The process performance was compared with the pulping and bleaching process for bamboo fiber. Several analytical methods, including field emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetry, and differential scanning calorimetry, were employed to determine the physicochemical and thermal properties of the treated cellulosic bamboo fiber. It was found that the pressurized enzyme hydrolysis treated bamboo fiber had the most uniform morphological structure, along with lowest crystallinity and highest thermal stability. Thus, utilizing high-pressure enzyme hydrolysis is the most effective process for treating fiber to remove non-cellulosic components from the raw material, including lignin, hemicelluloses, and waxy materials.

The effects of chlorite bleaching on the properties of cellulose derived from oil palm empty fruit bunch (OPEFB) fiber were investigated in this work. Cellulose was extracted from oil palm empty fruit bunch fiber via chlorite bleaching, alkali treatment, and acid hydrolysis. Cellulose was extracted by varying the bleaching duration, which corresponded to 4, 8, or 12 h. Fourier transform infrared (FTIR) analysis showed that the lignin and hemicellulose were significant removed after the bleaching process, whereas no spectral differences were observed in the samples with the increase of bleaching durations. The main removal of the lignin and hemicellulose components had occurred during the bleaching process. There was only slight additional removal of lignin and hemicellulose during the further extraction process with alkali and acid hydrolysis. The peaks at 1740 cm-1 and 1246 cm-1 which represent hemicellulose and lignin, respectively, were not present in the final extracted cellulose.The cellulose yield contents did not increase with the increasing of bleaching duration from 4 h to 12 h. X-ray diffraction (XRD) analysis revealed that the crystallinity and the 200 peak of OPEFB had increased after the bleaching process. Analysis of the visible light transmittance of cellulose, after a bleaching duration of 12 h, demonstrated the highest transmittance due to the disintegration of the fibers. By increasing the bleaching duration, the temperature at 50% weight loss of OPEFB increased, suggesting that the thermal stability of cellulose had improved.

One of the biggest disadvantages of wood, as a potential reinforcement for thermoplastics, is its hydrophilicity. The aim of this study was to evaluate the effect of chemical modification of wood flour on mechanical, thermal, and fire properties of filled high-density polyethylene composites. For this purpose, aspen flour was modified with maleic, propionic, and succinic anhydrides. The modified wood flour and high-density polyethylene were compounded into pellets by single-screw extrusion, and test samples were prepared by injection molding. Tensile and flexural tests, impact testing, limiting oxygen index, TGA, and SEM analyses were conducted both for modified and un-modified samples. Based on the test results, chemical modification enhanced the properties of thermoplastic composites. Depending on the chemical concentrations, the flexural, tensile, and impact strengths of the modified flour filled HDPE composites were improved slightly, while the tensile and flexural moduli of the samples were increased significantly. The limiting oxygen index (LOI) levels of samples with modified wood flour were slightly improved, and succinic anhydride provided higher LOI levels compared to the samples with other anhydrides. This showed that the composites filled with chemically modified wood flour were slightly more thermally stable than control samples. It appears that wood flour modified with maleic, propionic, and succinic anhydrides can be successfully utilized as filler in polymer matrices.

To investigate the properties of wood flour/high-density polyethylene composites (WF/HDPE) filled with different kinds of mineral components (CaCO3, talc powder, and wollastonite), WF/HDPE was prepared via a molding method. The thermal properties of WF/HDPE were analyzed with a comprehensive thermal analyzer, and the mechanical properties were measured. The moisture resistance was indicated by 24 h water absorption. The results indicated that both the mechanical and physical properties of WF/HDPE samples were improved remarkably by adding CaCO3, talc powder, or wollastonite. The tensile strength with talc powder was 83% higher than the composites without the additive. The maximum residual weight of the composites with added talc powder was 21.8% at 600°C, which was 7.47% higher than that of the composites without additive. The composites with added talc powder exhibited better water resistance. Additionally, scanning electron microscopy (SEM) showed that the addition of talc powder enhanced the interaction between the components. [ABSTRACT FROM AUTHOR]