Crystallization,mechanical properties,and enzymatic degradation of biodegradable poly(ε‐caprolactone) composites with poly(lactic acid) fibers

Biodegradable polymer composites based on poly(ɛ‐caprolactone) (PCL) and poly(lactic acid) (PLA) fibers were prepared by melt compounding. The effects of PLA fibers on the crystallization, mechanical properties, and enzymatic degradation of PCL composites were investigated. The addition of PLA fibers enhanced the crystallization of PCL due to the heterogeneous nucleation effect of fibers. However, the final crystallinity of the PCL in the composites was little changed in the presence of PLA fibers. With the addition of PLA fibers, significant improvement in storage modulus (E′) of PCL in the composites was achieved. A significant increase in E′ was 173% for the composites as compared to that of the neat PCL at 20°C. With the increase in PLA fibers content, the PCL composites showed decreased elongation and strength at break; however, the tensile yield strength and modulus were increased significantly, indicating that PCL was obviously reinforced by adding PLA fibers. Although the PLA fibers retarded the enzymatic degradation of PCL, it was possible to be completely degraded without much degradation time for PCL blending with suitable amounts of PLA fibers. POLYM. COMPOS., 34:1745–1752, 2013. © 2013 Society of Plastics Engineers     

Crystallization behavior of α‐cellulose short‐fiber reinforced poly(lactic acid) composites

The isothermal crystallization behavior of α‐cellulose short‐fiber reinforced poly(lactic acid) composites (PLA/α‐cellulose) was examined using a differential scanning calorimeter and a petrographic microscope. Incorporating a natural micro‐sized cellulose filler increased the spherulite growth rate of the PLA from 3.35 μm/min for neat PLA at 105°C to a maximum of 5.52 μm/min for the 4 wt % PLA/α‐cellulose composite at 105°C. In addition, the inclusion of α‐cellulose significantly increased the crystallinities of the PLA/α‐cellulose composites. The crystallinities for the PLA/α‐cellulose composites that crystallized at 125°C were 48–58%, higher than that of the neat PLA for ～13.5–37.2%. The Avrami exponent n values for the neat and PLA/α‐cellulose composites ranged from 2.50 to 2.81 and from 2.45 to 3.44, respectively, and the crystallization rates K of the PLA/α‐cellulose composites were higher than those of the neat PLA. The activation energies of crystallization for the PLA/α‐cellulose composites were higher than that of the neat PLA. The inclusion of α‐cellulose imparted more nucleating sites to the PLA polymer. Therefore, it was necessary to release additional energy and initiate molecular deposition. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effect of natural fibers on thermal and mechanical properties of natural fiber polypropylene composites studied by dynamic mechanical analysis

The present study deals with the effects of natural fibers on thermal and mechanical properties of natural fiber polypropylene composites using dynamic mechanical analysis. Composites of polypropylene and various natural fibers including kenaf fibers, wood flour, rice hulls, and newsprint fibers were prepared at 25 and 50% (by weight) fiber content levels. One and two percent maleic anhydride grafted polypropylene was also used as the compatibilizer for composites containing 25 and 50% fibers, respectively. Specimens for dynamic mechanical analysis tests were cut out of injection‐molded samples and were tested over a temperature range of ?60 to +120°C. Frequency of the oscillations was fixed at 1 Hz and the strain amplitude was 0.1%, which was well within the linear viscoelastic region. The heating rate was 2°C/min for all temperature scan tests. Storage modulus (E′), loss modulus (E″), and mechanical loss factor (tan δ) were collected during the test and were plotted versus temperature. An increase in storage and loss moduli and a decrease in the mechanical loss factor were observed for all composites indicating more elastic behavior of the composites as compared with the pure PP. Changes in phase transition temperatures were monitored and possible causes were discussed. Results indicated that glass transition was slightly shifted to lower temperatures in composites. α transition temperature was higher in the case of composites and its intensity was higher as well. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4341–4349, 2006     

Preparation and properties of successive alkali treated completely biodegradable short jute fiber reinforced PLA composites

The natural fiber reinforced biodegradable polymer composites were prepared with short jute fiber as reinforcement in PLA (Poly lactic acid) matrix. The short jute fiber is successively treated with NaOH at various concentrations (5%, 10%, and 15%) and H₂O₂. The composites were prepared with untreated and treated short jute fibers at different weight proportions (up to 25%) in PLA and investigated for mechanical properties. The results showed that the composite with successive alkali treated jute fiber at 10% NaOH and H₂O₂ with 20% fiber loading has shown 18% higher flexural strength than neat PLA and untreated jute/PLA composite. The flexural modulus of the composite at 25% fiber loading was 125% and 110% higher than that of composites with untreated fibers and neat PLA, respectively. The impact strength of composite with untreated fibers at higher fiber weight fraction was 23% high as compared to neat PLA and 26% high compared to composite with treated fibers. The water absorption was more for untreated jute/PLA composite at 25% fiber loading than all other composites. The composite with untreated fibers has high thermal degradation compared with treated fibers but lower than that of pure PLA matrix. The enzymatic environment has increased the rate of degradation of composites as compared to soil burial. Surface morphology of biodegraded surfaces of the composites were studied using SEM method. POLYM. COMPOS., 37:2160–2170, 2016. © 2015 Society of Plastics Engineers     

Thermal properties of extruded injection‐molded poly(lactic acid) and milkweed composites: Degradation kinetics and enthalpic relaxation

To determine the degree of compatibility between poly(lactic acid) (PLA) and different biomaterials, PLA was compounded with milkweed fiber, a new crop oil seed. After oil extraction, milkweed remaining cake retained approximately 10% residual oil, 47% protein, and 10% moisture. The fiber (300 μm) was added at 85 : 15 and 70 : 30 PLA : Fiber and blended by extrusion (EX) followed by injection molding (IM). Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) were used for testing the composites. After melting in the DSC sealed pans, composites were cooled by immersion in liquid nitrogen and aged (stored) at room temperature for 0, 7, 15, and 30 days. After storage, samples were heated from room temperature to 180°C at 10°C/min. The pure PLA showed a glass transition (T_g) at 60.3°C and the corresponding ΔCp was 0.464 J/g/°C followed by crystallization and melting transitions. The enthalpic relaxation (ER) of neat PLA and composites steadily increased as a function of storage time. Although the presence of fiber had little effect on ER, IM reduced it. The percentage crystallinity of neat unprocessed PLA dropped by 95 and 80% for the EX and IM, respectively. The degradation activation energy (E_a) of neat PLA exhibited a significant drop in nitrogen environment, whereas increased in air, indicating PLA resistant to heat degradation in the presence of oxygen. Overall, IM appeared to decrease E_a of the composites, whereas milkweed significantly reduced E_a values in nitrogen environment. Enzymatic degradation of the composites revealed higher degradation rate for the EX samples versus IM, whereas 30% milkweed exhibited higher weight loss compared to the 15%. The degradation mechanism was observed by looking at the percent conversion as a function of E_a from the TGA data, where multisteps degradation occurred mostly in air. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

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     

Chemical surface modification of wheat straw fibers for polypropylene reinforcement

The use of natural materials has grown in the last years in the plastics industry. Natural lignocellulose fibers derived from agricultural waste present potential to be used as a replacement for glass fibers for polymer reinforcement, leading to lower CO₂ footprint products. However, cellulose fibers are hydrophilic and polar and as a result of that, incompatible with hydrophobic polymers such as polypropylene. For this reason, a surface modification on the cellulose fiber is required. This work focuses on the modification of the cellulose fibers to improve the compatibility with polypropylene. Wheat straw fibers derived from agricultural waste were scoured with the purpose to remove lignin, hemicellulose and pectin to facilitate the defibrillation. The fibers were then esterified using acetic anhydride. Thermal gravimetric tests have shown an increase in the thermal stability of the scoured and esterified cellulose fibers, from 246°C for untreated fibers to 292°C and 316°C, respectively. From mechanical tests results it could be seen that the tensile modulus of the composites with esterified cellulose fibers increased 57% compared with the neat PP. Flexural strength increased by 31% and flexural modulus by 70%. The use of esterified fibers led to an improvement of 79% in the impact strength compared with the neat PP. A better compatibilization between fibers and matrix could be seen using maleic anhydride modified polypropylene copolymer as compatibilizer, even with esterified fibers, probably due to residual hydroxyl groups still available on modified cellulose. POLYM. COMPOS., 37:2133–2141, 2016. © 2015 Society of Plastics Engineers     

High‐strength biodegradable poly(vinyl alcohol)/fly ash composite films

We prepared biodegradable composite films of poly(vinyl alcohol) (PVA) and fly ash (FA) spanning 5, 10, 15, 20, and 25 wt % concentrations by casting aqueous solutions. The tensile strengths of the composite films were increased proportionally via the addition of FA. The strength of the film was enhanced by 193% with 20% FA compared to the neat PVA control. Further addition of FA deviated from the linear trend. The moduli of the composites also increased proportionally with FA addition to 212% at 20 wt % FA addition compared to the control. The percentage strain at break exponentially decreased with the addition of FA. In the dynamic mechanical behavior, the storage and loss moduli both increased with FA content. The tan δ peaks corresponding to the glass‐transition temperature shifted 5–10°C higher above the control sample (73°C). This shift was attributed to a reduction in the mobility of PVA segments because they were anchored by the FA surface. The reductions in mobility manifested in strong interfacial interactions were indicative of hydrogen bonding. Broadening and reduction in the intensities of the stretching and bending peaks of ? OH, ? CH and ? C?O of PVA in the Fourier transform infrared spectra were observed. This suggested that hydrogen bonding was active between the functional groups in the FA and PVA chains. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Mechanical properties and biodegradability of green composites based on biodegradable polyesters and lyocell fabric

Green composites composed of regenerated cellulose (lyocell) fabric and biodegradable polyesters [poly(3‐hydroxybutyrate‐co‐3‐hydroxyvarelate) (PHBV), poly(butylene succinate) (PBS), and poly(lactic acid) (PLA)] were prepared by compression‐molding method. The tensile moduli and strength of all the biodegradable polyester/lyocell composites increased with increasing fiber content. When the obtained PLA/lyocell composites were annealed at 100°C for 3 h, the tensile strength and moduli were lowered despite the increase of degree of crystallization of the PLA component. The SEM observation of the composites revealed that the surface of the annealed composite has many cracks caused by the shrinkage of the PLA adhered to lyocell fabric. Multilayered PLA/lyocell laminate composites showed considerably higher Izod impact strength than PLA. As a result of the soil viral test, although the order of higher weight loss for the single substance was lyocell > PHBV > PBS > PLA, the biodegradability of the green composites did not reflect the order of a single substance because of the structural defect of the composite. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3857–3863, 2004     

Physico-chemical,thermal, and mechanical properties of PLA-nHA nanocomposites: Effect of glass fiber reinforcement

In this study, tri-layered composites were prepared by reinforcing poly-lactic acid (PLA) nano-hydroxyapatite (n-HA) (1 and 5 wt%) and 20 mol% continuous phosphate glass fibers (PGF). Initially, the effect of addition of 1 and 5% n-HA on the structural, thermal, mechanical, and thermo-mechanical properties of 100% PLA was investigated. With 5 wt% n-HA addition the tensile modulus (TM), flexural modulus (FM), tensile strength (TS), and flexural strength (FS) of 100% PLA was improve by 14.9, 47.4, 6, and 32.9%, respectively. Whereas, the un-notched impact strength of the nanocomposites suffer 2% deterioration. However, T _g decreased by 0.3°C and T _c increased by 10°C as 5 wt% n-HA was added to 100% PLA. Afterwards, the 5% n-HA/PLA composite were reinforced with 20 mol% continuous PGF and the TM, FM, TS, and FS of the tri-layered composites were 162.6, 412.5, 28.4, and 157.4% higher as compared to 100%PLA. Furthermore, the storage modulus of the 1% n-HA-filled composites was 500 MPa lower than 100%PLA, while 5 wt% n-HA-filled composites showed similar storage modulus as 100% PLA. 5 wt% n-HA-filled composite showed the highest peak of loss modulus which may be attribute to the chain segment of PLA matrix after the incorporation of HA. Thus, n-HA and PGF reinforcement resulted in improved mechanical properties of the composites and have great potential as biodegradable bone fixation device with enhanced load-bearing ability.     

Mechanical properties of poly lactic acid composite films reinforced with wet milled jute nanofibers

In the present study, waste jute fibers generated in textile industries, were wet pulverized to the scale of nanofibers of 50 nm diameter using high energy planetary ball milling for 3 h. The presence of water during wet pulverization found to reduce the rising temperature of mill, which prevented sticking of nanofibers on the mill wall and resulted in unimodal size distribution. In the subsequent stage, 1, 5, and 10 wt% of jute nanofibers were incorporated in poly(lactic acid) (PLA) matrix to prepare nanocomposite films by solvent casting. The reinforcement of nanofibers was investigated from the improvements in mechanical properties based on tensile tests, dynamic mechanical analysis, and differential scanning calorimetry. The maximum improvement was observed in case of 5 wt% nanocomposite film where initial modulus and tensile strength increased by 217.30% and 170.59%, respectively as compared to neat PLA film. These improvements are attributed to the increased interaction between nanofibers and matrix as well as to the increased crystallinity of PLA in composites. The improvements in load bearing capacity of nanocomposite films were significant at 60°C than 35°C, which showed ability of jute nanofibers to improve the softening temperature of PLA matrix. In the end, experimental results of Young's modulus were compared with predicted modulus of mechanical models. A good level of agreement was observed up to 5 wt% loading of jute nanofibers. POLYM. COMPOS., 34:2133–2141, 2013. © 2013 Society of Plastics Engineers     

Water bamboo husk reinforced poly(lactic acid) green composites

The water bamboo husk is one of major agricultural wastes in Taiwan. In this study, the powder obtained from the water bamboo husk was added to poly(lactic acid) (PLA) to form novel reinforced biodegradable composites. Morphologies, mechanical properties, and heat resistance of these water bamboo powder reinforced composites were investigated. The results indicate that the char yields were increased as plant powder was incorporated to PLA. In addition, the mechanical properties were also enhanced due to the addition of powders. The increments of storage moduli of PLA were about 50–200%. Moreover, the increments of loss moduli of PLA were about 70–200%. On the other hand, the T_g of PLA was slightly decreased by the addition of powder, and this may improve the brittle characteristics of PLA. Furthermore, this type of reinforced PLA would be more environmental friendly than the artificial additive‐reinforced one. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Flax fiber‐reinforced polylactide stereocomplex composites with enhanced heat resistance and mechanical properties

Polylactide stereocomplex (sc‐PLA) prepared by blending equivalent proportion of poly(l ‐lactic acid)/poly(d ‐lactic acid) (PLLA/PDLA) and its composites reinforced with 10, 20, and 30% flax fibers were fabricated by melt compounding and followed by injection molding. The mechanical properties, crystallinity, cross‐section morphology, and heat resistance of sc‐PLA and flax/sc‐PLA composites were compared. The results showed that homocrystallites (hc) and stereocomplex crystallites (sc) were formed simultaneously in sc‐PLA and its composites, with a melting temperature at ∼170 and ∼210°C, respectively. The crystallinity and sc content of composite increased with the increasing content of the flax fibers. The sc content of 30% flax/sc‐PLA composite could reach 98.4%, 32% higher than that of sc‐PLA (66.4%). When compared with nonblended PLLA, heat resistance of sc‐PLA increased slightly, but at the expense of mechanical properties. By the addition of flax fibers, the mechanical properties of flax/sc‐PLA composite improved significantly. The highest tensile strength, Young's modulus, and notched Izod impact strength of flax/sc‐PLA composite were 52.90 MPa, 6.42 GPa, and 5.27 kJ/m², respectively, improved by 54, 132, and 343% when compared with sc‐PLA. Moreover, the heat resistance of composite was also improved greatly by reinforcing with flax fibers. The Vicat softening temperature of 30% flax/sc‐PLA composite could achieve 162.5°C, nearly 100°C higher than that of PLLA. POLYM. COMPOS., 38:472–478, 2017. © 2015 Society of Plastics Engineers     

Thermal behavior of vinyl ester resin matrix composites reinforced with alkali‐treated jute fibers

The thermal behavior of vinyl ester resin matrix composites reinforced with jute fibers treated for 2, 4, 6, and 8 h with 5% NaOH was studied with Thermo‐gravimetric analysis and differential scanning calorimetry. The moisture desorption peak shifted to a higher temperature, from 37 to 58.3°C, for all the treated‐fiber composites because of improved wetting of the fibers by the resin and stronger bonding at the interface. The degradation temperature of the vinyl ester resin in the composites was lowered to 410.3°C from that of the neat resin, 418.8°C. The X‐ray diffraction studies showed increased crystallinity of the treated fibers, which affected the enthalpy of the α‐cellulose and hemicellulose degradation. The hemicellulose degradation temperature remained the same (299.7°C) in all the treated‐fiber composites, but the enthalpy associated with the hemicellulose degradation showed an increasing trend in the treated composites with a small increase in the weight loss. This could be attributed to the increased hydrogen bonding between the more accessible ? OH groups of the hemicellulose in the noncrystalline region of the jute fiber and the resin. The degradation temperature of α‐cellulose was lowered from 364.2 to 356.8°C in the treated composites. The enthalpy of α‐cellulose degradation showed a decreasing trend with a lowering of the weight loss. The crystalline regions of the fiber, consisting of closely packed α‐cellulose chains, were bonded with the resin mainly on the surface through hydrogen bonds and became more resistant to thermal degradation; this reduced the weight loss. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 123–129, 2004     

Rubber–clay nanocomposite by solution blending

Ethylene vinyl acetate rubber (45% vinyl acetate content, EVA‐45) and organomodified clay (12Me‐MMT) composites were prepared by solution blending of the rubber and the clay. A combination of X‐ray diffraction, scanning electron microscopy, and transmission electron microscopy studies showed that the composites obtained are on the nanometer scale. The measurements of the dynamic mechanical properties for different compositions over a temperature range (?100 to +100°C) showed that the storage moduli of these rubber–clay nanocomposites are higher above the glass to rubber transition temperature compared to the neat rubber. The tensile strength of the nanocomposites is about 1.6 times higher than that of the EVA‐45. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 2216–2220, 2003     

Reuse of natural fiber reinforced eco‐composites in polymer mortars

In this article, the results of the design of recycling–reuse facilities for transformation of solid–polymer composite waste into polymer mortars and concrete structures for the low‐cost building industry have been presented. Thermoplastic polymer matrix composites based on polylactic acid (PLA) reinforced with natural fibers (rice husks and kenaf fibers) have been recycled and reused as reinforcement. Polymer mortars with unsaturated polyester resin as a binder (commercially available orthophthalic liquid polyester with 35% monomer content) have been prepared by mixing foundry sand and milled recycled eco‐composites (milled size of 0.050 mm) in mix proportions of 40/20/40 ^%/_% wt. The obtained materials have been analyzed with standard test methods (mechanical tests, thermogravimetrical analysis (TGA), dynamic‐mechanical analysis (DMTA), differential scanning calorimtery (DSC), and scanning electron microscopy (SEM)). POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers     

Effect of plasticizer on the crystallization behavior of poly(lactic acid)

In this article, the spherulitic morphology and growth rate of the neat and plasticized poly(lactic acid) (PLA) with triphenyl phosphate (TPP) were compared and analyzed by polarizing optical microscopy with hot stage at a temperature range of 100?142°C. The spherulitic morphology of the neat PLA underwent a series of changes such as the typical Maltese Cross at less than 132°C, the disappearance of the Maltese Cross at 133°C, the irregular and distorted spherulites at higher than 134 and 142°C, respectively. For plasticized PLA, the spherulitic morphology exhibited the same changes as neat PLA, but these changes were shifted to lower temperature when compared with neat PLA. In the case of the spherulitic growth, neat PLA had the maximum value of 0.28 μm/s at 132°C, and plasticized PLA had higher values than that of neat PLA. Further analysis based on the Lauritzen–Hoffman theory was presented and results showed that the values of nucleation parameter K_g increased with TPP content. The crystallization behavior of PLA was analyzed by differential scanning calorimetry and wide‐angle X‐ray diffraction. The results showed that the degree of crystallinity of plasticized PLA markedly increased when compared with neat PLA sharply with the incorporation of plasticizer. The crystallization kinetics for the neat and plasticized PLA under isothermal crystallization at 114°C was described by the Avrami equation and the Avrami exponent is close to 2, implying that the crystallization mechanism did not change. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Composites of poly(lactic acid) with flax fibers modified by interstitial polymerization

Natural fiber composites were designed and optimized to achieve good mechanical properties and resistance to growth of living organisms. Composite materials were prepared from poly(lactic acid) (PLA) with flax fibers, which had been subjected to interstitial polymerization to replace the water in the cellulose fibers. Prior to the polymerization, the flax fibers were extracted with sodium hydroxide and acetone to remove lignin, pectin, and waxes from the cellulose. Differential scanning calorimetry was used to study the crystallization and melting of the composites compared to pure PLA. The surface wetting of the fibers and morphology of the composites were studied by scanning electron microscopy and optical microscopy. Mechanical properties were studied using dynamic mechanical analysis. The influence of the interstitial polymerization on the dynamic storage modulus was found to be significant. The composites of polymerization treated flax with acetone washed fibers had higher storage moduli than the unwashed fiber composites, which suggested that the adhesion between the flax fibers and the matrix was improved by the treatments. The composites were subjected to moist environmental conditions in order to test for development of mold and fungi, and the acetone washed polymerization treated flax composites were resistant to these growths. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3620–3629, 2006     

Fabrication and evaluation of some mechanical and electrical properties of jute‐biomass based hybrid composites

Hybrid composites based on bisphenol‐C‐formaldehyde resin and jute mat with rice, wheat, sugar cane, and jamun husks have been fabricated at 150°C under 30.4 MPa pressure for 2 h. The resin content in composites was 50% of fibers. Tensile strength, flexural strength, electric strength, and volume resistivity of hybrid composites have been evaluated and compared with those of jute‐bisphenol‐C‐formaldehyde composites. It is observed that the tensile strength of composites is found to decrease by 53–72%, which is mainly due to random orientation of sandwiched fibers. Flexural strength has increased by 53–153% except jute–rice husk composite for which it is decreased by 26%. A little change in dielectric breakdown strength (1.89–2.11 kV/mm) is found but volume resistivity of Jute–wheat husk and Jute–jamun husk composites has improved by 437–197% and it is slightly decreased(2.3–25.2%) for the remaining two composites. Thus, hybrid composites possess good mechanical and electrical properties signifying their importance in low strength and light weight engineering applications as well as low cost housing units such as partition and hard boards. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1754–1758, 2006     

Kinetics and crystal structure of isothermal crystallization of poly(lactic acid) plasticized with triphenyl phosphate

In this article, the spherulitic growth rate of neat and plasticized poly(lactic acid) (PLA) with triphenyl phosphate (TPP) was measured and analyzed in the temperature range of 104–142°C by polarizing optical microscopy. Neat PLA had the maximum value of 0.28 μm/s at 132°C, whereas plasticized PLA had higher value than that of neat PLA, but the temperature corresponding to the maximum value was shifted toward lower one with increasing TPP content. The isothermal crystallization kinetics of neat and plasticized PLA was also analyzed by differential scanning calorimetry and described by the Avrami equation. The results showed for neat PLA and its blends with various TPP contents, the average value of Avrami exponents n were close to around 2.5 at two crystallization temperatures of 113 and 128°C, the crystallization rate constant k was decreased, and the half‐life crystallization time t_1/2 was increased with TPP content. For neat PLA and its blend with 15 wt % TPP content, the average value of n was 2.0 and 2.3, respectively, the value of k was decreased, and the value of t_1/2 was increased with crystallization temperature (T_c). Further investigation into crystallization activation energy ΔE_a of neat PLA and its blend with 15 wt % TPP showed that ΔE_a of plasticized PLA was increased compared to neat PLA. It was verified by wide‐angle X‐ray diffraction that neat PLA and its blends containing various TPP contents crystallized isothermally in the temperature range of 113–128°C all form the α‐form crystal. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010