Physico‐mechanical and decay resistance properties of chemically modified tropical wood material

In this present research, several kinds of selected tropical light hardwoods were chemically modified with benzene diazonium salt to improve their physico‐mechanical and decay resistance properties. Benzene diazonium salt underwent a coupling reaction with wood which was confirmed through fourier transform infrared spectroscopic analysis. The compressive modulus of the treated wood increased, whereas modulus of rupture was shown to decrease on treatment. Water absorption was also found to decrease considerably after modification. The modified wood samples had higher hardness (Shore D) value compared to that of the control ones. The wood was exposed to two types of fungi; white‐rot (Polyporus versicolor) and brown‐rot (Postia placenta), for 12 weeks and then decay was assessed through weight loss percentage (%). A significant improvement was found in the modified wood compared to the control wood. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effects of fungal decay on properties of mechanical,chemical, and water absorption of wood plastic composites

This study investigated the associations between wood species and fungal resistance, as well as the effects of fungal decay on the properties of mechanical, chemical, and water absorption of wood polypropylene composites (WPCs) filled with white poplar, moso-bamboo, Chinese fir, Ramin, white pine, and rubber wood. Experimental results on weight losses and surface morphology both showed that fungal resistance of WPCs varied significantly with wood fiber species. Chinese fir and rubber wood filled composites separately presented the most and least durability against Coriolus versicolor (white rot) and Poria placenta (brown rot). In addition, fungal decay produced great differences in the properties of mechanical, chemical, and water absorptions between non-decayed and decayed composites. The decayed composites showed lower MOR, tensile strength, and impact strength, as well as higher MOE and water absorptions compared with non-decayed samples. These findings suggest that fungal decay could bring out dramatic influences on various properties of WPCs.     

Weathering,water absorption,and durability of silicon,acetylated, and heat‐treated wood

In this study, two colloidal dispersions of pure amorphous silicon dioxide particles, acetylated, and heat‐treated samples were tested for a possible application as a wood protection agents. The silicon, acetylated, and heat‐treated samples were exposed to an accelerated weathering experiment, and their dimensional stability was assessed. The weathering experiment comprised cycles of 2 h UV‐light irradiation followed by water spray for 18 min. The surface changes of the weathered samples were characterized by FT‐IR spectroscopy and color measurements. According to results, the silicon treatments showed lower color changes than untreated ones. However, acetylated and heat‐treated samples provided the lowest color changes. The resistance of the silicon, acetylated, and heat‐treated wood to decay was studied by means of brown and white rot fungi in laboratory decay tests. Decay test results revealed that acetylated and heat‐treated wood samples showed better decay resistance against P. placenta and C. versicolor than silicon treatments. Samples modified with silicon were exposed in above ground standard lap‐joint test in Ultuna, Sweden. The dispersions of pure amorphous silicon dioxide impregnated in wood did not significantly influence its hygroscopic and dimensional behavior. However, the silicon treatment reduced the color changes caused by weathering. The silicon impregnated samples showed a weak fungal discoloration similar to that of chromated copper arsenate impregnated controls in above ground standard lap‐joint test. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4506–4513, 2006     

Bio-based Epoxy Resins from Epoxidized Plant Oils and Their Shape Memory Behaviors

In this study, bio‐based epoxy materials containing functionalized plant oil, such as epoxidized soybean oil (ESO) and epoxidized linseed oil (ELO), were processed with 4‐methylhexahydrophthalic anhydride (MHPA) as a curing agent. In the presence of tetraethylammonium bromide, the curing reaction of epoxidized plant oil and MHPA proceeded at 130 °C to give transparent plant oil‐based epoxy materials. The resulting bio‐based epoxy materials exhibited relatively soft and flexible characters, due to the aliphatic chains of plant oil. The thermal and mechanical properties of the ESO/MHPA polymers depended on the feed molar ratio of anhydride to oxirane. The mechanical properties such as tensile strength and Young's modulus of the ELO/MHPA polymer increased, compared with those of the ESO/MHPA polymer. The glass transition temperature of the ELO/MHPA polymer was higher than that of the ESO/MHPA polymer, because of the high oxirane number of ELO. Furthermore, the ELO/MHPA polymer showed excellent shape memory property.     

Significant enhancement of fracture toughness and mechanical properties of epoxy resin using CTBN-grafted epoxidized linseed oil

Carboxyl-terminated poly(acrylonitrile-co-butadiene) (CTBN)-grafted epoxidized linseed oil (ELO) (CTBN-g-ELO) was synthesized and used as an effective toughener to simultaneously enhance the mechanical properties and fracture toughness of epoxy resin (EP). The ELO was fabricated from linseed oil via epoxidation processing. The characteristics of the ELO and CTBN-g-ELO, such as the average molecular weight and chemical structure, were determined using gel permeation chromatography, proton nuclear magnetic resonance, and Fourier transform infrared spectroscopy. The effects of the CTBN-g-ELO loading on the characteristics of the EP were investigated in detail. The test results indicated that by adding 15 phr CTBN-g-ELO, the tensile strength, impact strength, and critical stress intensity factor (K_IC) were significantly increased, by approximately 23.62, 91.8, and 33.8%, respectively, compared with pristine EP. The glass-transition temperature (T_g) and storage modulus, which were examined via dynamic mechanical thermal analysis and differential scanning calorimetry, respectively, exhibited decreasing trends. Scanning electron microscopy revealed that the CTBN-g-ELO existed as spherical particles in the EP, helping to stop the crack growth and change the crack growth directions. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48276.     

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     

Evaluation of dimensional stability,weathering and decay resistance of modified pine wood by in-situ polymerization of styrene

Abstract

In this study, polystyrene modified Scots pine (Pinus sylvestris L.) wood was investigated upon artificial weathering, decay resistance, dimensional stability and water uptake properties. Polystyrene modification was carried out on pretreated wood by immersion of wood into styrene monomer and further polymerization. The resistance of modified wood against cycles of UV and water exposures was examined by artificial weathering test for 672?hours, and decay resistance was evaluated by attacks of Coniophora puteana and Trametes versicolor on the samples. During the artificial weathering, color and surface roughness of the samples, and macroscopic changes were determined periodically. Changes in the surface chemistry and morphology of the weathered samples were investigated by ATR-FTIR and SEM, respectively. It was proven that polystyrene effectively protected pine samples from both fungi even after leaching procedure, but it was more effective in preventing C. puteana attacks than T. versicolor attacks. As a result of artificial weathering, the surface of all samples was darkened. However, changes in color and roughness as well as crack formations of the modified sample surfaces were found less than those of the untreated samples. Polystyrene also provided considerable improvement on dimensional stability, as well as water repellence of wood.     

Agro‐wastes: Mechanical and physical properties of resin impregnated oil palm trunk core lumber

Agro‐wastes, oil palm trunk core or sap was utilized for the production of new palm‐wood material using phenol formaldehyde resin as a matrix. The kiln‐dried (moisture content 10%) oil palm trunk was impregnated with phenol formaldehyde resin using a high power vacuum pump. The oil palm trunk core lumber (OPTCL) was loaded with different percentages of phenol formaldehyde (PF) resin. The mechanical properties (tensile, flexural, and impact) and physical properties (water absorption and density) were studied and compared with rubberwood. Testing of mechanical and physical properties was done according to the ASTM standard. The morphology of the resin loaded OPTCL was analyzed by using Scanning Electron Microscopy (SEM). In general, the result showed that impregnated OPTCL exhibited good mechanical and physical properties when compared with untreated oil palm trunk core (OPTCL with 0% resin content) and rubberwood. Tensile and flexural strength of OPTCL increased with the increase in the resin content up to 15% and showed a decreasing trend with the increase in the loading percentage beyond 15%.The impact strength also increased with the increase in the resin content from 5% to 15%. However, impregnated OPTCL with 15% resin loading showed lower water absorption uptake as compared with the other composite materials and rubberwood. SEM micrograph confirmed that the resin was impregnated efficiently within the pores of OPTCL fibers. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Synthesis and characterization of new vinyl acetate grafting onto epoxidized linseed oil in aqueous media

Modified poly (vinyl acetate) copolymers with epoxidized linseed oil (ELO) as co‐monomer have been prepared. The polymerization was performed in aqueous medium without any additional protective colloid in the presence of sodium persulfate as catalyst. The effect of vinyl acetate (VAc)/ELO feed ratio, reaction temperature, reaction time, and catalyst amount has been studied. FTIR spectroscopy showed that the reaction between ELO and VAc resulted in slight decrease and shift in ELO characteristic bands of oxirane groups; and new bands were detected in the copolymer spectra attributed to PVAc and ELO functional groups. Moreover, new signals attributable to the copolymer were observed in the ¹H NMR spectra (δ 4.07 and 1.62 ppm) and in the ¹³C NMR spectra (δ 15.29 and 31.0 ppm). Analysis by differential scanning calorimetry (DSC) showed a single T_g for the copolymerization product of VAc and ELO and two T_g for the PVAc/ELO blend, indicating the chemical reaction between VAc and ELO. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42089.     

Photo‐fabricated unsaturated polyester resin composites reinforced by kenaf fibers,synthesis and characterization

New bio‐fiber composites (UPRC) cured by ultraviolet radiation were produced using kenaf fiber as reinforcing agent and unsaturated polyester resins as matrix in the presence of styrene and IRGACURE 1800 as photoinitiator. Unsaturated polyester resins based on palm oil were prepared from various ratios of monoglyceride (MG)/maleic anhydride (MA) by the interaction of the corresponding MG monomer, with different equivalents of MA, in the presence of 2‐methylimidazole as catalyst. The various characteristics of the obtained bio‐fiber composites, including mechanical, gel content, water absorption and thickness swelling test, thermal analysis, were determined and the data were discussed. Bio‐fiber composite with MG: MA ratio (1 : 4 eq./eq.) showed better mechanical properties (tensile, flexural, and impact strength) than other formulations. Gel content increased as the amount of MA was increased up to the MG: MA ratio was 1 : 4 (eq./eq.) then slightly decreased at the higher ratio formulation. Bio‐fiber composite (UPRC_c) was considered the best prepared bio‐fiber composite which contained higher degree double bond, cross‐linking and thermal stability. Moreover, morphological study of selected examples of the formed bio‐fiber composites was also carried out and showed the evidence of the enhancement of the compatibility between fiber and polymer matrix. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Mechanical properties,flame retardancy,hot‐air ageing,and hot‐oil ageing resistance of ethylene‐vinyl acetate rubber/hydrogenated nitrile‐butadiene rubber/magnesium hydroxide composites

The mechanical properties, flame retardancy, hot‐air ageing, and hot‐oil ageing resistance of ethylene‐vinyl acetate rubber (EVM)/hydrogenated nitrile‐butadiene rubber (HNBR)/magnesium hydroxide (MH) composites were studied. With increasing HNBR fraction, elongation at break and tear strength of the EVM/HNBR/MH composites increased, whereas the limited oxygen index and Shore A hardness decreased slightly. Hot‐air ageing resistance and hot‐oil ageing resistance of the composites became better with increasing HNBR fraction. Thermal gravimetric analysis results demonstrated that the presence of MH and low HNBR fraction could improve the thermal stability of the composites. Differential scanning calorimeter revealed that the glass transition temperature (T_g) of the composites shifted toward low temperatures with increasing HNBR fraction, which was also confirmed by dynamic mechanical thermal analysis. Atomic force microscope images showed MH has a small particle size and good dispersion in the composites with high HNBR fraction. The flame retardancy, extremely good hot‐oil ageing, and hot‐air ageing resistance combined with good mechanical properties performance in a wide temperature range (?30°C to 150°C) make the EVM/HNBR/MH composites ideal for cables application. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of maleic anhydride/vinyltrimethoxysilane‐co‐grafting polypropylene on the properties of wood‐flour/polypropylene composites by electron‐beam preirradiation

The electron‐beam preirradiation and reactive extrusion technologies were used to prepare maleic anhydride (MAH)/vinyltrimethoxysilane (VTMS)‐co‐grafting polypropylene (PP) as a high‐performance compatibilizer for wood‐flour/PP composites. The grafting content, chemical structure, and crystallization behavior of the compatibilizers were characterized through Fourier transform infrared spectroscopy, differential scanning calorimetry, and an extraction method. The effects of the compatibilizers on the mechanical properties, water absorption, morphological structure, and torque rheological behavior of the composites were investigated comparatively. The experimental results demonstrate that MAH/VTMS‐g‐PP markedly enhanced the mechanical properties of the composites. Compared with MAH‐g‐PP and VTMS‐g‐PP, MAH/VTMS‐g‐PP clearly showed synergistic effects on the increasing mechanical properties, water absorption, and compatibility of the composites. Scanning electron microscopy further confirmed that the adhesion and dispersion of wood flours in the composites were effectively improved by MAH/VTMS‐g‐PP. These results were also proven by the best water resistance of the wood‐flour/PP composites with MAH/VTMS‐g‐PP. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of different crosslinkers on properties of melamine formaldehyde‐furfuryl alcohol copolymer/montmorillonite impregnated softwood (Ficus hispida)

Melamine formaldehyde‐furfuryl alcohol (MFFA) copolymer was prepared and impregnated into softwood Ficus hispida in combination with crosslinking agent and montmorillonite (MMT) under vacuum condition. Different crosslinkers namely n‐methylol acrylamide, (NMA), 2‐hydroxyethyl methacrylate (HEMA) and 1,3‐dimethylol‐4,5‐dihydroxyethyleneurea (DMDHEU) were used for evaluation of properties of the prepared composites. Nuclear magnetic resonance (NMR) and fourier transform infrared spectroscopy (FTIR) studies confirmed the formation of MFFA copolymer, NMA, and DMDHEU crosslinkers. X‐ray diffractometry (XRD) and FTIR studies were used to characterize the nanocomposites. The incorporation of MMT decreased the crystallinity of wood composites as revealed by XRD study. Maximum interaction was found in wood samples treated with MFFA/(NMA+HEMA+DMDHEU)/MMT as shown by FTIR study. The incorporation of MMT into the wood polymer composite was revealed by transmission electron microscopy study. Thermal stability and flammability were checked by thermogravimetric analyzer and limiting oxygen index instrument. Wood treated with MFFA, blended crosslinker and MMT exhibited higher dimensional stability, lower water uptake (%), enhanced chemical resistance, and better mechanical properties (flexural, tensile, and hardness). SEM study indicated the presence of polymer and MMT in the void spaces of wood. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Hydrophobic sponge for spilled oil absorption

As the ecological damage caused by marine oil spills has become one main threat to marine ecological security, materials that can reduce environmental pollution are in high demand. In this study, a simple low‐cost method for fabricating a hydrophobic polyurethane sponge was investigated. Its hydrophobicity was evaluated through the measurement of the contact angles of water and oil. The mechanical properties, oil‐absorption capacity, and selectivity were also tested. The results show that this sponge exhibited good mechanical properties, a high absorption capacity and selectivity, and a high reusability (>200 times) in oil–water separation. More importantly, the absorbed oil could be collected by simple squeezing. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40886.     

Synthesis and properties of polyurethane elastomers based on renewable castor oil polyols

In this contribution, castor oil polyols with functionality of f = 2.7 and f = 2 are used as soft segments (SS) for synthesizing polyurethane elastomers (PUEs) without addition of petroleum-based polyol. The effect of molar ratio of castor oil polyols on structure and properties of PUEs has been investigated by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, dynamic mechanical analysis, X-ray diffraction, tensile, swelling, and water absorption tests. The results reveal that hydrogen bonding mainly exists in hard segments (HSs) and weakens with decreasing the molar percentage of castor oil polyol (f = 2.7) in SS. T _g of SS decreases while T _g of HS remains constant as molar percentage of castor oil polyol (f = 2.7) decreased. The initial degradation temperatures (T_5%) are above 300 °C and independent of the molar ratio of castor oil polyols. However, the temperature at 50% weight loss (T_50%) decreases significantly as molar percentage of castor oil polyol (f = 2.7) decreased. Moreover, PUEs exhibit very low water absorption rate, <1%, after immersing in water for 140 h at room temperature. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47309.     

Synthesis and properties of a ternary polyacrylate copolymer resin for the absorption of oil spills

A high‐oil‐absorption resin of a ternary copolymer for the absorption of oil spills was successfully prepared by suspension polymerization, and characterizations of the oil‐absorption resin were also examined in this study. The high‐oil‐absorption resin, a ternary copolymerized long‐chain polyacrylate with styrene (St), butyl methacrylate (BMA), and stearyl methacrylate (SMA) as the monomers and synthesized by suspension polymerization, was introduced. The oil‐absorption resin of St/BMA/SMA was characterized by Fourier transform infrared spectrometry. The particle morphology of the resin was observed by scanning electron microscopy. The effects of different polymerization technological parameters, such as the mass ratios of the monomer, the benzoyl peroxide initiator, and the crosslinking agent of divinylbenzene; the sort and concentrations of the dispersing agent of hydroxyl ethyl cellulose, sodium dodecyl benzene sulfonate, and gelatin, and the polymerization temperature, on the oil absorbency of St/BMA/SMA are discussed in detail. The optimum polymerization conditions of the St/BMA/SMA copolymer were obtained as follows: m_St/m_monomer = 50 wt %, m_BMA/m_{soft monomer} = 60 wt %, m_water/m_oil = 3:1, m_DVB/m_monomer = 1.0 wt %, m_BPO/m_monomer = 1.5 wt %, m_HEC/m_monomer = 0.07 wt %, m_SDBS/m_monomer = 0.03 wt %, m_gelatin/m_monomer = 0.14 wt % (where m is the mass), temperature = 85°C. With increasing content of these factors, the oil absorbency increased at first and then decreased. Compared with binary copolymer St/BMA prepared in previous research, the highest oil absorbencies to dichloromethane were 12.80 and 23.00 g/g in the St/BMA and St/BMA/SMA copolymers, respectively. St/BMA/SMA had a higher oil absorbency and faster oil‐adsorbing rate than St/BMA. The oil absorption in the oil–water mixture and the recovery of the resin were also studied in detail. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40180.     

Building and origin of bio‐based bismaleimide resins with good processability,high thermal,and mechanical properties

Bio‐based high performance thermosetting resins have been urgently required by cutting‐edge fields for meeting sustainable development. A new kind of high performance thermosetting resins (BA‐n) with good processability, high thermal resistance, and mechanical properties was developed based on 4,4′‐bismaleimidodiphenylmethane (BDM) and renewable bis(5‐allyloxy)‐4‐methoxy‐2‐methylphenyl)methane (ABE) from bio‐based lignin derivative. The effect of the molar ratio of allyl to imide (n) on structures and properties of BA resins were systematically researched. BA‐n resins have much better processability, thermal, and mechanical properties than their petroleum‐based counterparts, 2,2′‐diallylbisphenol A‐modified BDM (BD‐n) resins. Compared with BD‐0.86, the best available bismaleimide (BMI) resin, BA‐0.86 not only has 6 h longer process window and 13.7 °C higher glass transition temperature, but also owns the highest flexural strength and modulus among all bio‐based allyl compound‐modified BMI resins reported. The origin behind these attractive performances of BA resins is revealed by discussing the unique crosslinked structure. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45947.     

Hard wood‐composites made of rice straw and recycled polystyrene foam wastes

The submitted work discussed the possibility of using two of the most problematic wastes to formulate an added‐value hard wood‐composite (HWC). The lignocellulosic rice straws (RS) fibers (as reinforced filler) and recycled expanded polystyrene foam (PS) wastes (as dispersed polymer matrix), were used to formulated the hard wood product applying the hot press technique. The air dried RS was added to the molten PS at increasing ratios (30–70% mass:mass), and the reached HWC sheet was subjected to tensile strength, water absorption and acoustic resistance characterizations. Based on the experimental data, it was found that increasing the RS contents accompanied with a diminish in the tensile strength value by about 50% at 70% RS compare to that at 30% RS. To improve the adhesion between the hydrophilic filler RS and the hydrophobic PS matrix, maleated PS graft (PS‐g‐MA) was prepared and added at the expanse of the PS content, to formulate an additional wood‐composite (HWCg) aiming to have better mechanical and dimensional stability features. Results obtained indicated that increasing the coupling agent content, keeping the RS added constant, enhance the tensile strength feature in addition, reduced the water absorption for the final products by more than 45%. The data obtained suggested that, it can create added‐value hard wood composites entirely from the two nominated problematic wastes. In addition to the value gained by the environment, the reached hard wood products record acceptable mechanical characterization, dimensional stability and sound resistance properties that qualified it to replace the natural wood in many daily applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44770.     

Effect of polyvinylpyrrolidone molecular weights on morphology,oil/water separation,mechanical and thermal properties of polyetherimide/polyvinylpyrrolidone hollow fiber membranes

We prepared polyetherimide (PEI) hollow fiber membranes using polyvinylpyrrolidones (PVP) with different molecular weights (PVP 10,000, PVP 40,000, and PVP 1,300,000) as additives for oil/water separation. Asymmetric hollow fiber membranes were fabricated by wet phase inversion technique from 25 wt % or 30 wt % solids of 20 : 5 : 75 or 20 : 10 : 70 (weight ratio) PEI/PVP/N‐metyl‐2‐pyrrolidone (NMP) solutions and a 95 : 5 NMP/water solution was used as bore fluid to eliminate resistance on the internal surface. Effects of PVP molecular weights on morphology, oil‐surfactant‐water separation characteristics, mechanical, and thermal properties of PEI/PVP hollow fiber membranes were investigated. It was found that an increase in PVP molecular weight and percentage in PEI/PVP dope solution resulted in the membrane morphology change from the finger‐like structure to the spongy structure. Without sodium hypochlorite posttreatment, hollow fiber membranes with higher PVP molecular weights had a higher rejection but with a lower water flux. For oil‐surfactant‐water emulsion systems (1600 ppm surfactant of sodium dodecylbenzenesulfonate and 2500 ppm oil of n‐decane), experimental results illustrated that the rejection rates for surfactant, total organic carbon, and oil were 76.1 ≈ 79.8%, 91.0 ≈ 93.0%, and more than 99%, respectively. Based on the glass transition temperature values, PVP existed in hollow fiber membranes and resulted in the hydrophilicity of membranes. In addition, using NaOCl as a posttreatment agent for membranes showed a significant improvement in membrane permeability for PVP with a molecular weight of 1300 K, whereas the elongation at break of the treated hollow fiber membranes decreased significantly. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2220–2233, 1999     

An investigation of sound absorption coefficient on sisal fiber poly lactic acid bio‐composites

In this research, the mechanical, acoustical, thermal, morphological, and infrared spectral properties of untreated, heat and alkaline‐treated sisal fiber‐reinforced poly‐lactic‐acid bio‐composites were analyzed. The bio‐composite samples were fabricated using a hot press molding machine. The properties mentioned above were evaluated and compared with heat‐treated and alkaline‐treated sisal fibers. Composites with heat‐treated sisal fibers were found to exhibit the best mechanical properties. Thermo‐gravimetric analysis (TGA) was conducted to study the thermal degradation of the bio‐composite samples. It was discovered that the PLA‐sisal composites with optimal heat‐treated at 160°C and alkaline‐treated fibers possess good thermal stability as compared with untreated fiber. The results indicated that the composites prepared with 30wt % of sisal had the highest sound absorption as compared with other composites. Evidence of the successful reaction of sodium hydroxide and heat treatment of the sisal fibers was provided by the infrared spectrum and implied by decreased bands at certain wavenumbers. Observations based on scanning electron microscopy of the fracture surface of the composites showed the effect of alkaline and heat treatment on the fiber surface and improved fiber‐matrix adhesion. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42470.