Effects of alkali and silane treatment on the mechanical properties of jute‐fiber‐reinforced recycled polypropylene composites

Jute‐fibers‐reinforced thermoplastic composites are widely used in the automobile, packaging, and electronic industries because of their various advantages such as low cost, ease of recycling, and biodegradability. However, the applications of these kinds of composites are limited because of their unsatisfactory mechanical properties, which are caused by the poor interfacial compatibility between jute fibers and the thermoplastic matrix. In this work, four methods, including (i) alkali treatment, (ii) alkali and silane treatment, (iii) alkali and (maleic anhydride)‐polypropylene (MAPP) treatment, and (iv) alkali, silane, and MAPP treatment (ASMT) were used to treat jute fibers and improve the interfacial adhesion of jute‐fiber‐reinforced recycled polypropylene composites (JRPCS). The mechanical properties and impact fracture surfaces of the composites were observed, and their fracture mechanism was analyzed. The results showed that ASMT composites possessed the optimum comprehensive mechanical properties. When the weight fraction of jute fibers was 15%, the tensile strength and impact toughness were increased by 46 and 36%, respectively, compared to those of untreated composites. The strongest interfacial adhesion between jute fibers and recycled polypropylene was obtained for ASMT composites. The fracture styles of this kind of composite included fiber breakage, fiber pull‐out, and interfacial debonding. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers.     

Unsaturated polyester‐toughened epoxy composites: Effect of sisal fiber on thermal and dynamic mechanical properties

In the present study, the mechanical and thermal properties of sisal fiber‐reinforced unsaturated polyester (UP)‐toughened epoxy composites were investigated. The sisal fibers were chemically treated with alkali (NaOH) and silane solutions in order to improve the interfacial interaction between fibers and matrix. The chemical composition of resins and fibers was identified by using Fourier‐transform infrared spectroscopy. The UP‐toughened epoxy blends were obtained by mixing UP (5, 10, and 15 wt%) into the epoxy resin. The fiber‐reinforced composites were prepared by incorporating sisal fibers (10, 20, and 30 wt%) within the optimized UP‐toughened epoxy blend. Scanning electron microscopy was used to analyze the morphological changes of the fibers and the adhesion between the fibers and the UP‐toughened epoxy system. The results showed that the tensile and flexural strength of (alkali‐silane)‐treated fiber (30 wt%) ‐reinforced composites increased by 83% and 55%, respectively, as compared with that of UP‐toughened epoxy blend. Moreover, thermogravimetric analysis revealed that the (alkali‐silane)‐treated fiber and its composite exhibited higher thermal stability than the untreated and alkali‐treated fiber systems. An increase in storage modulus and glass transition temperature was observed for the UP‐toughened epoxy matrix on reinforcement with treated fibers. The water uptake behavior of both alkali and alkali‐silane‐treated fiber‐reinforced composites is found to be less as compared with the untreated fiber‐reinforced composite. J. VINYL ADDIT. TECHNOL., 23:188–199, 2017. © 2015 Society of Plastics Engineers     

Study on poly(butylene adipate‐co‐terephthalate)/starch composites with polymeric methylenediphenyl diisocyanate

To lower the cost of poly(butylene adipate‐co‐terephthalate) or PBAT, starch was used as a filler in this study. To increase tensile strength of PBAT/starch composites, polymeric methylenediphenyl diisocyanate (pMDI) was used as a compatibilizer. PBAT was melt‐mixed with starch in a kneader, and then the mixtures were compression‐molded. The effects of starch and pMDI content on the tensile strength and elongation at break of PBAT/starch composites were examined. The morphology and biodegradability of the composites in soil were also studied. The tensile strength of PBAT and PBAT/starch composites increases with increasing content of pMDI. The increase of weight average molecular weight of PBAT and improved interaction between PBAT and starch were observed with increasing content of pMDI. The weight average molecular weights of buried PBAT and the composites in soil significantly decrease. Especially, the reduction of the weight average molecular weight of PBAT/starch (70/30) composite is the most significant. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41884.     

Effect of silane coupling agents on basalt fiber–epoxidized vegetable oil matrix composite materials analyzed by the single fiber fragmentation technique

The fiber–matrix interfacial shear strength (IFSS) of biobased epoxy composites reinforced with basalt fiber was investigated by the fragmentation method. Basalt fibers were modified with four different silanes, (3‐aminopropyl)trimethoxysilane, [3‐(2‐aminoethylamino)propyl]‐trimethoxysilane, trimethoxy[2‐(7‐oxabicyclo[4.1.0]hept‐3‐yl)ethyl]silane and (3‐glycidyloxypropyl)trimethoxysilane to improve the adhesion between the basalt fiber and the resin. The analysis of the fiber tensile strength results was performed in terms of statistical parameters. The tensile strength of silane‐treated basalt fiber is higher than the tensile strength of the untreated basalt fiber; this behavior may be due to flaw healing effect on the defected fiber surfaces. The IFSS results on the composites confirm that the interaction between the fiber modified with coupling agents and the bio‐based epoxy resin was much stronger than that with the untreated basalt fiber. POLYM. COMPOS., 36:1205–1212, 2015. © 2014 Society of Plastics Engineers     

Surface treatment of phosphate glass fibers using 2‐hydroxyethyl methacrylate: Fabrication of poly(caprolactone)‐based composites

2‐Hydroxyethyl methacrylate (HEMA) solution (1–10 wt %) was prepared in methanol and phosphate glass fibers were immersed in that solution for 5 min before being cured (irradiation time: 30 min) under UV radiation. Maximum polymer loading (HEMA content) was found for the 5 wt % HEMA solution. Degradation tests of the fibers in aqueous medium at 37°C suggested that the degradation of the HEMA‐treated fibers was lower than that of the untreated fibers. X‐ray photoelectron spectroscopy revealed that HEMA was present on the surface of the fibers. Using 5 wt % HEMA‐treated fibers, poly(caprolactone) matrix unidirectional composites were fabricated by in situ polymerization and compression molding. For in situ polymerization, it was found that 5 wt % HEMA‐treated fiber‐based composites had higher bending strength (13.8% greater) and modulus (14.0% greater) than those of the control composites. For compression molded composites, the bending strength and modulus values for the HEMA‐treated samples were found to be 27.0 and 31.5% higher, respectively, than the control samples. The tensile strength, tensile modulus, and impact strength of the HEMA composites found significant improvement than that of the untreated composites. The composites were investigated by scanning electron microscopy after 6 weeks of degradation in water at 37°C. It was found that HEMA‐treated fibers inside the composite retained much of their original integrity while the control samples degraded significantly. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

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.     

Bamboo fibers @ poly(ethylene glycol)‐reinforced poly(butylene succinate) biocomposites

The poly(poly(ethylene glycol) methyl ether methacrylate)‐ (PPEGMA)‐grafted bamboo fiber (BF) (BF@PPEGMA) was successfully synthesized via the esterification and atom transfer radical polymerization (ATRP) methods. The poly(butylenes succinate) (PBS) matrix‐based composites including BF and BF@PPEGMA were prepared by a twin‐screw extruder. The structure, morphology, as well as the properties of BF@PPEGMA and composites was investigated. The results indicated that PPEGMA was successfully grafted onto the BF surfaces, making BF surfaces rough and less thermally stable. The BF@PPEGMA showed of stronger interactions with PBS matrix than pristine BF, leading to the improvement of tensile modulus, tensile strength, and elongation at break of the composites. The PBS/BF@PPEGMA composites absorbed less water than PBS/BF composites due to the existence of less content of hydroxyl groups after surface modification. Incorporation of BF and BF@PPEGMA facilitated the crystallization of PBS at higher temperatures, leading to formation of regular spherulites without appearance of transcrystallization. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Ultraviolet resistance modification of poly(p‐phenylene‐1,3,4‐oxadiazole) and poly(p‐phenylene terephthalamide) fibers with polyhedral oligomeric silsesquioxane

Octa‐ammonium chloride salt of polyhedral oligomeric silsesquioxane (POSS) was synthesized by a hydrolysis reaction and introduced into poly(p‐phenylene‐1,3,4‐oxadiazole) (p‐POD) and poly(p‐phenylene terephthalamide) (PPTA) fibers by a finishing method to enhance the UV resistance. The effects of the POSS concentration, treatment temperature, and time on the tensile strength of the fibers were investigated. The surface morphology, mechanical properties, crystallinity, degree of orientation of fibers, and intrinsic viscosity of the polymer solution were characterized in detail. The results indicate that the tensile strength retention and intrinsic viscosity retention of the fibers treated with POSS were much higher than those of the untreated fibers after the same accelerated irradiation time; this demonstrated that this treatment method was feasible. We also found that the efficacy of the protection provided by POSS was more beneficial to p‐POD than PPTA because of the different structure. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42643.     

Dynamic mechanical analysis of oil palm microfibril‐reinforced acrylonitrile butadiene rubber composites

The dynamic mechanical properties of microfibers of oil palm‐reinforced acrylonitrile butadiene rubber (NBR) composites were investigated as a function of fiber content, temperature, treatment, and frequency. The storage modulus (E′) was found to increase with weight fraction of microfibrils due to the increased stiffness imparted by the strong adhesion between the polar matrix and the hydrophilic microfibrils. The damping properties were found to decrease with increase in fiber loading. As the fiber content increases, the damping nature of the composite decreases because of the increased stiffness imparted by the natural fibers. By steam explosion method (STEX), microfibrils are separated from fibers. Natural fibers were undergone treatment such as mercerization, benzoylation, and silane treatment. The NBR is modified by the addition of resorcinol‐hexa‐hydrated silica (HRH) bonding agent. Also dicumyl peroxide (DCP) is used as an alternating vulcanizing agent in the system. In the case of composites containing chemically modified fibers, storage modulus were found to increase. Cole–Cole analysis was made to study the phase behavior of the composite samples. Activation energy for the relaxation processes in different composites was calculated. Morphological studies using scanning electron microscopy of tensile fracture surfaces of treated and untreated composites indicated better fiber matrix/adhesion in the case of treated microfibril‐reinforced composites. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Preparation and properties of L‐lactide‐grafted sisal fiber–reinforced poly(lactic acid) composites

Pretreatment of the sisal fiber (SF) grafting with L‐lactide (LA) monomer via a ring‐opening polymerization catalyzed by a Sn(II)‐based catalyst was performed to improve the interfacial adhesion between SF and poly (lactic acid) (PLA). Biocomposites from LA‐grafted SF (SF‐g‐LA) and PLA were prepared by compression molding with fiber weight fraction of 10, 20, 30, and 40%, and then were investigated in contrast with alkali‐treated sisal fiber (ASF) reinforced PLA composites and untreated SF reinforced PLA composites. PLA composites reinforced by half‐and‐half SF‐g‐LA/untreated SF (half SF‐g‐LA) were prepared and studied as well, considering the disadvantages of SF‐g‐LA. The results showed that both the tensile properties and flexural properties of the SF‐g‐LA reinforced PLA composites were improved noticeably as the introduction of SF‐g‐LA, compared with pure PLA, untreated SF reinforced PLA composites and ASF reinforced PLA composites. The mechanical properties of the half SF‐g‐LA reinforced PLA composites were not worse, even better in some aspects, than the SF‐g‐LA reinforced PLA composites. Fourier transform infrared analysis and differential scanning calorimetry analysis exhibited that both the chemical composition and crystal structure of the SFs changed after LA grafting. In addition, the fracture surface morphology of the composites was studied by scanning electron microscopy. The morphological studies demonstrated that a better adhesion between LA‐grafted SF and PLA matrix was achieved. POLYM. COMPOS., 37:802–809, 2016. © 2014 Society of Plastics Engineers     

Mechanical,thermal, and water absorption properties of melamine–formaldehyde‐treated sisal fiber containing poly(lactic acid) composites

The present study focuses on the melamine–formaldehyde (MF) coating ratio and silanization of PLA/sisal composites. Poly(lactic acid) (PLA) was melt blended with short sisal fiber with and without MF resin coating. MF was applied at different weight ratios (sisal:MF = 1:1; 1:3, and 1:5) to coat the untreated or silanized sisal fibers which were incorporated up to 20 parts per hundred resin (phr) amount in PLA. PLA/sisal composites were produced by compression molding. It was found that the sisal:MF coating ratio at 1:1 by weight improved the tensile strength and tensile modulus of the composite with 10 phr sisal by 4% and 57%, respectively, compared to the virgin PLA. The initial and final decomposition (T_i) and (T_f) of PLA with untreated sisal were changed from 330.8 and 367.1 to 336.2 and 370.4 °C, respectively, after MF‐coating (sisal:MF weight ratio = 1:1). This enhancement in thermal stability was attributed to the strong interaction between the MF and sisal fiber. The water absorption of PLA/MF–sisal composites slightly decreased with increasing sisal:MF ratio. This is due to the fact that the MF‐coating substantially reduced the hydrophilic properties of sisal. Moreover, FTIR spectra and SEM images proved that sisal fibers were coated by MF resin successfully. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45681.     

Concentration effect of γ‐glycidoxypropyltrimethoxysilane on the mechanical properties of glass fiber–epoxy composites

In this study, glass fibers were modified using γ‐glycidoxypropyltrimethoxysilane of different concentrations to improve the interfacial adhesion at interfaces between fibers and matrix. Effects of γ‐glycidoxypropyltrimethoxysilane on mechanical properties and fracture behavior of glass fiber/epoxy composites were investigated experimentally. Mechanical properties of the composites have been investigated by tensile tests, short beam tests, and flexural tests. The short‐beam method was used to measure the interlaminar shear strength (ILSS) of laminates. The tensile and flexural properties of composites were characterized by tensile and three‐point bending tests, respectively. The fracture surfaces of the composites were observed with a scanning electron microscope. On comparing the results obtained for the different concentrations of silane solution, it was found that the 0.5% GPS silane treatment provided the best mechanical properties. The ILSS value of heat‐cleaned glass fiber reinforced composite is enhanced by ∼59% as a result of the glass fiber treatment with 0.5% γ‐GPS. Also, an improvement of about 37% in tensile strength, about 78% in flexural strength of the composite with the 0.5% γ‐GPS treatment of glass fibers was observed. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Wood‐fiber‐reinforced poly(lactic acid) composites: Evaluation of the physicomechanical and morphological properties

This article presents the results of a study of the processing and physicomechanical properties of environmentally friendly wood‐fiber‐reinforced poly(lactic acid) composites that were produced with a microcompounding molding system. Wood‐fiber‐reinforced polypropylene composites were also processed under similar conditions and were compared to wood‐fiber‐reinforced poly(lactic acid) composites. The mechanical, thermomechanical, and morphological properties of these composites were studied. In terms of the mechanical properties, the wood‐fiber‐reinforced poly(lactic acid) composites were comparable to conventional polypropylene‐based thermoplastic composites. The mechanical properties of the wood‐fiber‐reinforced poly(lactic acid) composites were significantly higher than those of the virgin resin. The flexural modulus (8.9 GPa) of the wood‐fiber‐reinforced poly(lactic acid) composite (30 wt % fiber) was comparable to that of traditional (i.e., wood‐fiber‐reinforced polypropylene) composites (3.4 GPa). The incorporation of the wood fibers into poly(lactic acid) resulted in a considerable increase in the storage modulus (stiffness) of the resin. The addition of the maleated polypropylene coupling agent improved the mechanical properties of the composites. Microstructure studies using scanning electron microscopy indicated significant interfacial bonding between the matrix and the wood fibers. The specific performance evidenced by the wood‐fiber‐reinforced poly(lactic acid) composites may hint at potential applications in, for example, the automotive and packaging industries. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4856–4869, 2006     

Biodegradable composites of poly(butylene succinate‐co‐butylene adipate) reinforced by poly(lactic acid) fibers

Biodegradable composites of poly(butylene succinate‐co‐butylene adipate) (PBSA) reinforced by poly(lactic acid) (PLA) fibers were developed by hot compression and characterized by Scanning electron microscopy (SEM), differential scanning calorimetry (DSC), dynamic mechanical analyzer, and tensile testing. The results show that PBSA and PLA are immiscible, but their interface can be improved by processing conditions. In particular, their interface and the resulting mechanical properties strongly depend on processing temperature. When the temperature is below 120 °C, the bound between PBSA and PLA fiber is weak, which results in lower tensile modulus and strength. When the processing temperature is higher (greater than 160 °C), the relaxation of polymer chain destroyed the molecular orientation microstructure of the PLA fiber, which results in weakening mechanical properties of the fiber then weakening reinforcement function. Both tensile modulus and strength of the composites increased significantly, in particular for the materials reinforced by long fiber. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43530.     

Covalent functionalization of carbon fiber with poly(acrylamide) by reversible addition–fragmentation chain transfer polymerization for improving carbon fiber/epoxy interface

A novel method was developed for grafting poly(acrylamide) (PAAM) on to the carbon fiber (CF) surface via reversible addition–fragmentation chain transfer (RAFT) polymerization to improve the interaction between carbon fibers and epoxy matrix in the composites system. The carbon fibers were first treated with nitric acid and γ‐methacryloxypropyltrimethoxy silane (KH570). Then, the PAAM was grafting onto the carbon fiber surface via RAFT polymerization. The resulted carbon fibers functionalized with PAAM (CF‐PAAM) were characterized by FTIR, XPS, and TGA, and the results revealed that CF‐PAAM were synthesized successfully. The introduction of PAAM chains could make the fiber surface rougher and introduce a large numbers of –NH₂ groups, which can improve the interfacial adhesion in the composites. The microbond test results showed that the interfacial shear strength (IFSS) of the composites reinforced by CF‐PAAM has been enhanced about 107%. POLYM. COMPOS., 38:27–31, 2017. © 2015 Society of Plastics Engineers     

Biodegradation of poly(butylene adipate‐co‐butylene terephthalate)/layered‐silicate nanocomposites

The biodegradability of poly(butylene adipate‐co‐butylene terephthalate) (PBAT) and PBAT/starch composites with layered silicates prepared by melt intercalation was evaluated with aerobic biodegradability tests in soil and in an aqueous medium containing activated sludge. Nonmodified montmorillonite (MMT) and octadecylamine‐modified montmorillonite (ODA‐M), known to give a microcomposite and an intercalated nanocomposite for PBAT, respectively, were used as layered silicates. After they were buried in the soil for 8 months, the PBAT/MMT microcomposite exhibited a higher weight loss than the control PBAT, whereas the PBAT/ODA‐M nanocomposite showed a lower weight loss instead. Also, the biodegradability test in the aqueous medium, by determining the biochemical oxygen demand, showed that the addition of MMT and/or starch to PBAT promoted biodegradation, whereas the addition of ODA‐M did not. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

High‐performance copoly(benzimidazole‐benzoxazole‐imide) fibers: Fabrication,structure, and properties

Novel high‐performance copolyimide (co‐PI) fibers containing benzimidazole and benzoxazole ring in the main chain were prepared by a two‐step spinning via the poly(amic acid)s. Effects of the incorporated benzimidazole and benzoxazole units on the micro‐structure and properties of co‐PI fibers were investigated. Fourier transform infrared (FTIR) results indicated that hydrogen bonding is formed in the co‐PI fibers. The co‐PI fibers exhibited discernible crystallization peaks at 14°～15° and 23°～26° (2θ), showing crystalline‐like structure. Moreover, the packing type of benzimidazole‐imide units determined the macromolecules packing of co‐PIs. It was amazedly found that the co‐PI fibers exhibited higher tensile strength and initial modulus than those of corresponding homo‐PI fibers, reaching tensile strength of 2.2–2.6 GPa, initial modulus of 99.1–113.2 GPa. The results of dynamic mechanical analysis (DMA) indicated co‐PI2 fiber had a positive T_g deviation due to the presence of strong intermolecular hydrogen bonding between benzimidazole‐imide and benzoxazole‐imide units, which maybe lead to the effective stress transfer between benzimidazole‐imide units and benzoxazole‐imide units. In addition, the obtained PI fibers exhibited excellent thermal properties with the 10% weight loss temperatures under N₂ in the range of 574–585°C. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42001.     

Thermal properties of extruded/injection‐molded poly(lactic acid) and biobased composites

To determine the degree of compatibility between poly(lactic acid) and different biomaterials (fibers), poly(lactic acid) was compounded with sugar beet pulp and apple fibers. The fibers were added in 85 : 15 and 70 : 30 poly(lactic acid)/fiber ratios. The composites were blended by extrusion followed by injection molding. Differential scanning calorimetry and thermogravimetric analysis were used to analyze the extruded and extruded/injection‐molded composites. After melting in sealed differential scanning calorimetry pans, the composites were cooled through immersion in liquid nitrogen and aged (stored) at room temperature for 0, 7, 15, and 30 days. After storage, the samples were heated from 25 to 180°C at 10°C/min. The neat poly(lactic acid) showed a glass‐transition transition at 59°C with a change in heat capacity (ΔC_p) value of 0.464. The glass transition was followed by crystallization and melting transitions. The enthalpic relaxation of the poly(lactic acid) and composites steadily increased as a function of the storage time. Although the presence of fibers had little effect on the enthalpic relaxation, injection molding reduced the enthalpic relaxation. The crystallinity percentage of the unprocessed neat poly(lactic acid) dropped by 95% after extrusion and by 80% for the extruded/injection‐molded composites. The degradation was performed in air and nitrogen environments. The degradation activation energy of neat poly(lactic acid) exhibited a significant drop in the nitrogen environment, although it increased in air. This meant that the poly(lactic acid) was more resistant to degradation in the presence of oxygen. Overall, injection molding appeared to reduce the activation energy for all the composites. Sugar beet pulp significantly reduced the activation energy in a nitrogen environment. In an air environment, both sugar beet pulp and apple fibers increased the activation energy. The enzymatic degradation of the composites showed a higher degradation rate for the extruded samples versus the extruded/injection‐molded composites, whereas the apple composites exhibited higher weight loss. The thermogravimetric analysis data showed that the degradation of unprocessed and extruded neat poly(lactic acid) followed a one‐step mechanism, whereas extruded/injection‐molded composites showed two‐step degradation. A higher fiber content resulted in up to three‐step degradation mechanisms. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Moisture uptake and resulting mechanical response of bio‐based composites. II. composites

The durability of entirely bio‐based composites with respect to the exposure to elevated humidity was evaluated. Different combinations of bio‐based resins (Tribest, EpoBioX, Envirez) and cellulosic fibers (flax and regenerated cellulose fiber rovings and fabrics) were used to manufacture unidirectional and cross‐ply composite laminates. Water absorption experiments were performed at various humidity levels (41%, 70%, and 98%) to measure apparent diffusion coefficient and moisture content at saturation. Effect of chemical treatment (alkali and silane) of fibers as protection against moisture was also studied. However, fiber treatment did not show any significant improvement and in some cases the performance of the composites with treated fibers was lower than those with untreated reinforcement. The comparison of results for neat resins and composites showed that moisture uptake in the studied composites is primarily due to cellulosic reinforcement. Tensile properties of composites as received (RH = 24%) and conditioned (RH = 41%, 70%, and 98%) were measured in order to estimate the influence of humidity on behavior of these materials. Results were compared with data for glass fiber reinforced composite, as a reference material. Previous results from study of unreinforced polymers showed that resins were resistant to moisture uptake. Knowing that moisture sorption is primarily dominated by natural fibers, the results showed that some of the composites with bio‐based resins performed very well and have comparable properties with composites of synthetic epoxy, even at elevated humidity. POLYM. COMPOS., 36:1510–1519, 2015. © 2014 Society of Plastics Engineers     

Water bamboo husk‐reinforced poly(butylene succinate) biodegradable composites

The water bamboo husk is one of major agricultural wastes in Taiwan. In this study, the fiber and powder obtained from the water bamboo husk were chemically modified by coupling agents. Furthermore, the modified fiber and powder were added to the biodegradable polymer poly(butylene succinate) (PBS) separately, to form novel fiber‐reinforced composites. Morphologies, mechanical properties, and heat resistance of these water bamboo husk‐reinforced composites were investigated. The results indicate that the fibers modified by coupling agents exhibited better compatibility with the polymer matrixes than did the untreated fibers. Moreover, it is found that the thermal properties were improved as plant fiber was incorporated to those polymers. Furthermore, the mechanical properties were also increased with the addition of coupling agent‐treated fiber. On the other hand, it is found that the homogeneity of untreated powder‐containing samples is better than that of untreated fiber‐containing samples. Moreover, the results reveal that the powders modified with coupling agents were not effective in improving the mechanical properties of the reinforced PBS. This is due to the bulky structure of lignin leading to a smaller reaction ratio with the coupling agents. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 188–199, 2006