The influence of the preparation conditions and filler content on thermal properties of poly‐l‐lactide and hydroxyapatite/poly‐l‐lactide nanocomposite

Poly‐l ‐lactide (PLLA) and hydroxyapatite/poly‐l ‐lactide (HAp/PLLA) are two widely used biomaterials for three‐dimensional scaffolds, drug release matrices and implantable medical devices for reparation of bone tissue; diversity in the initial preparation and filler content has a significant influence on different properties such as morphology and crystallinity, thus playing a considerable role in most of these applications. For this reason, PLLA and HAp/PLLA samples with a large difference in crystallinity (from below 20% to over 70%) and filler content (up to 86 wt% of HAp nanoparticles with an average diameter of 80 nm) were prepared and consequent dissimilarities in morphology, crystallinity and thermal properties were investigated by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), wide angle X‐ray diffraction (WAXD) measurements and Fourier transform infrared (FTIR) spectroscopy. Special attention was devoted to analyzing data obtained from thermal measurements. A three‐phase model was employed in order to describe the heat capacity step decline in the nanocomposite; the evolution in different polymer fractions, the crystalline fraction and the mobile and rigid amorphous fractions, with filler content was determined. © 2017 Society of Chemical Industry     

Biocompatibility and strengthening of porous hydroxyapatite scaffolds using poly(l-lactic acid) coating

Hydroxyapatite (HA) is a well-known biocompatible bone substitute. Porous HA is more resorbable and osteoconductive compared with non-porous HA, and has been studied both experimentally and clinically. However, the mechanical strength of porous HA scaffolds is known to be weak. In this study, we developed a porous HA scaffold coated with a synthetic biodegradable polymer, poly(l-lactic acid) (PLLA), to strengthen the scaffold. PLLA-coated HA pellets were used to investigate the in vitro proliferation and alkaline phosphatase (ALP) activity of osteoblasts. PLLA-coated porous HA scaffolds were observed using scanning electron microscopy to investigate surface characteristics, porosity, and mechanical strength. PLLA coating concentration varied from 2 to 10 wt%. Osteoblast proliferation was higher in HA samples coated with PLLA compared with non-coated. ALP activity was highest on 8 wt% PLLA-coating after 3 days and on 4 wt% and 6 wt% PLLA after 9 and 12 days. Porous HA scaffolds with higher concentrations of PLLA were found to have a smoother, flatter surface. This enhanced proliferation and attachment of osteoblasts onto the porous HA scaffold. PLLA solution at a concentration of 10 wt% decreased scaffold porosity to half that of HA scaffolds with no PLLA coating. Scaffold mechanical strength was increased two-fold with a PLLA concentration of 2 wt%. Based on in vitro experimentation, it can be concluded that PLLA-coating on porous HA scaffolds enhances both the biocompatibility and the mechanical strength.     

Enhanced mechanical properties of acrylate based shape memory polymer using grafted hydroxyapatite

In the present study, the effect of grafted and ungrafted hydroxyapatite (HAp) filler on the mechanical properties of acrylate based shape memory polymer (SMP) composite is reported. HAp is grafted with polyethylene glycol methacrylate (PEGMA) monomer to avoid agglomeration and the same is embedded as reinforcement in tBA – PEGDMA matrix (70 wt% tBA: tert-butyl acrylate +30 wt% PEGDMA: polyethylene glycol dimethacrylate). The grafting process improved the interfacial interactions of the particles, dispersed in the polymer system and subsequently enhanced the mechanical properties of the shape memory polymer composites. The morphology of HAp particles is investigated by field emission scanning electron microscopy. The mechanical properties of SMP composites are evaluated at room temperature and above glass transition temperature (Tg) with grafted and ungrafted HAp particles. The addition of grafted HAp significantly improved the tensile strength (40%) and shape recovery rate (25%) of the SMP composite when compared to the SMP composite containing ungrafted HAp. SMP composite containing grafted HAp exhibited higher cell viability compared to the neat SMP and the SMP composite containing ungrafted HAp.     

Electrically conducting biodegradable polymer composites (polylactide‐polypyrrole and polycaprolactone‐polypyrrole) for passive resonant circuits

Electrically conducting biodegradable polymer composites made of polypyrrole (PPy) nanoparticles embedded in poly(L ‐lactide) (PLLA) or poly(ε‐caprolactone) (PCL) are prepared by chemical oxidative polymerization. They will be used as electrical conductors for fabricating biodegradable passive resonant circuits for bioimplants. For both composites, the conductivity exhibits a percolation threshold at ～6 wt% of PPy. Several reactants are tested, the polymerization process resulting in the highest conductivity uses iron(III)chloride hexahydrate (FeCl₃), sodium dodecyl benzene sulfonate, and p‐nitrophenol (pNPh), for both poly(L ‐lactide)‐polypyrrole (PLLA‐PPy) and poly(ε‐caprolactone)‐polypyrrole (PCL‐PPy). Conductivities of 2.7 ± 0.8 S cm^ε1 (PLLA‐PPy) and 7.8 ± 2.3 S cm^?1 (PCL‐PPy) are reached for a PPy content of 40 wt%. The PPy particle, observed by SEM, forms agglomerates having a size of 0.6–3.5 μm. The samples have similar PPy particle distributions over the entire cross sections. The conductivity as a function of time is investigated, being 34–70% of the initial value for samples stored in nitrogen, whereas it is less than 1% for samples stored in body‐like conditions, bringing the conclusion that a biodegradable packaging will be required to protect the resonant circuits from body fluids. Finally, the biocompatibility of the polymer composites is evaluated with cytocompatibility tests on dermal human fibroblast cells, showing promising results in particular for composites having a low PPy content. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

The electrical properties and crystallization of stereocomplex poly(lactic acid) filled with carbon nanotubes

Multi-walled carbon nanotubes (MWCNTs) filled poly(l-lactic acid) (PLLA) and PLLA/poly(d-lactic acid) (PDLA) composites were prepared through a directly melt mixing process. A special crystalline structure of stereocomplex was formed by PLLA and PDLA, which was easily found when mixing two polymers with identical chemical composition but different steric structures. The electrical conductivities were greatly improved by the formation of stereocomplex compared to that of PLLA/MWCNT composites at same MWCNT content. The percolation threshold of the PLLA/PDLA/MWCNT composite at a PLLA/PDLA weight ratio of 50/50 was 0.35 wt%, while being 1.43 wt% of PLLA/MWCNT composites. The X-ray diffraction, non-isothermal and isothermal crystallization results showed that the formation of stereocomplex greatly increased the crystallinity of the composites, meanwhile MWCNTs acted as heterogeneous nucleating agent, which significantly accelerated the nucleation and spherulite growth. Therefore, the PLLA/PDLA/MWCNT composites have a very low percolation threshold due to the volume exclusion effect.     

Electrospun poly(L‐lactic acid)/hydroxyapatite composite fibrous scaffolds for bone tissue engineering

Poly(L ‐lactic acid) (PLLA) is one of the most studied synthetic biodegradable polymeric materials as a bone graft substitute. Taking into account the osteoconductive property of hydroxyapatite (HAp), we prepared fibrous matrices of PLLA without and with HAp particles in amounts of 0.25 or 0.50% (w/v, based on the volume of the base 15% w/v PLLA solution in 70:30 v/v dichloromethane/tetrahydrofuran). These fibrous matrices were assessed for their potential as substrates for bone cell culture. The presence of HAp in the composite fibre mats was confirmed using energy dispersive X‐ray spectroscopy mapping. The average diameters of both neat PLLA and PLLA/HAp fibres, as determined using scanning electron microscopy, ranged between 2.3 and 3.5 µm, with the average spacing between adjacent fibres ranging between 5.7 and 8.5 µm. The porosity of these fibrous membranes was high (ca 97–98%). A direct cytotoxicity evaluation with L929 mouse fibroblasts indicated that the neat PLLA fibre mats released no substance at a level that was toxic to the cells. The presence of HAp particles at 0.50% w/v in the PLLA fibrous scaffolds not only promoted the attachment and the proliferation of MC3T3‐E1 mouse pre‐osteoblastic cells, but also increased the expression of osteocalcin mRNA and the extent of mineralization after the cells had been cultured on the scaffolds for 14 and 21 days, respectively. The results obtained suggested that the PLLA/HAp fibre mats could be materials of choice for bone tissue engineering. Copyright © 2009 Society of Chemical Industry     

The effect of filler content on mechanical properties and cell response of elastomeric PGS/apatite foam scaffolds

Poly(glycerol sebacate) (PGS) is a novel polymeric material intended for applications in tissue engineering (TE). This study involves synthesizing the PGS prepolymer (pPGS) and subsequent manufacturing of porous PGS-based scaffolds with an addition of hydroxyapatite (HAp) by means of thermally induced phase separation followed by thermal cross-linking and salt-leaching (TIPS-TCL-SL). The study aims to investigate the effect of the apatite filler content on properties and morphology of porous PGS/HAp scaffolds. The emphasis is put on the mechanical behavior of the material characterized by means of compression tests and dynamic thermal mechanical analysis (DMTA). In addition to the reference polymer scaffold, the composites with filler contents of 10, 20 and 30 wt% have been examined. Our research revealed that the HAp content does not affect the mechanical properties in a directly proportional manner. The 30 wt% addition of HAp resulted in frayed structure and decrease in the mechanical parameters in comparison to other tested specimens. On the other hand, an addition of 10% did not sufficiently boost the properties. Therefore, a 20% addition of HAp was concluded to have superior mechanical properties in comparison to other analyzed specimens. A similar relationship results from the DMTA studies. Moreover, the strain sweep and frequency sweep tests confirmed the stability of the mechanical parameters in various conditions, as well as the elastomeric nature of the materials. Finally, the material did not exhibit cytotoxicity against standard L929 fibroblasts and cells readily populated the scaffolds.     

Electrical conductivity properties of expanded graphite–polycarbonatediol polyurethane composites

Conductive polymer composites of segmented polycarbonatediol polyurethane and expanded graphite (EG) have been synthesized with different amounts of EG conductive filler (from 0 to 50 wt%). SEM, X‐ray diffraction measurements, Fourier transform infrared and Raman spectroscopies demonstrated a homogeneous dispersion of the EG filler in the matrix. The dielectric permittivity of the composites showed an insulator to conductor percolation transition with increase in EG content. Significant changes in the dielectric permittivity take place when the weight fraction of EG is in the range 20–30 wt%. Special attention has been paid to the dependence of the conductivity on frequency, temperature and EG content. The addition of EG to the matrix causes a dramatic increase in the electrical conductivity of 10 orders of magnitude, which is an indication of percolative behavior. A percolation threshold of ca 30 wt% was evaluated by using the scaling law of percolation theory. © 2014 Society of Chemical Industry     

Effects of red mud on rheological,crystalline, and mechanical properties of red mud/PBAT composites

This work presents the potential use of red mud (RM), which is a waste of industrial alumina, as a filler of a biodegradable polymer, poly(butylene adipate‐co‐terephthalate) (PBAT), to prepare environment friendly composite materials (RM/PBATs). The rheological properties and crystallization behavior of RM/PBAT composites with different contents of RM (0, 10, 20, 30, 40, and 50 wt%) were investigated in detail. After incorporating of RM, the crystalline temperature of PBAT was greatly improved. When the content of RM was 30 wt%, the crystalline temperature was up to 96.0°C which widened its' use. The rheological properties of the composites such as the storage modulus, loss modulus, and viscosity as well as the melting and crystalline temperature of the composites were also increased, whereas the crystallinity was slightly decreased with the increasing of RM. The prepared composite is expected in the future to be used for packaging materials. The scanning electron microscopy (SEM) was used to investigate the dispersion of RM in the PBAT matrix which had direct effect on the above properties. POLYM. COMPOS., 37:2001–2007, 2016. © 2015 Society of Plastics Engineers     

Fabrication of an Electrically-Resistive,Varistor-Polymer Composite

This study focuses on the fabrication and electrical characterization of a polymer composite based on nano-sized varistor powder. The polymer composite was fabricated by the melt-blending method. The developed nano-composite was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FeSEM), and energy-dispersive X-ray spectroscopy (EDAX). The XRD pattern revealed the crystallinity of the composite. The XRD study also showed the presence of secondary phases due to the substitution of zinc by other cations, such as bismuth and manganese. The TEM picture of the sample revealed the distribution of the spherical, nano-sized, filler particles throughout the matrix, which were in the 10–50 nm range with an average of approximately 11 nm. The presence of a bismuth-rich phase and a ZnO matrix phase in the ZnO-based varistor powder was confirmed by FeSEM images and EDX spectra. From the current-voltage curves, the non-linear coefficient of the varistor polymer composite with 70 wt% of nano filler was 3.57, and its electrical resistivity after the onset point was 861 KΩ. The non-linear coefficient was 1.11 in the sample with 100 wt% polymer content. Thus, it was concluded that the composites established a better electrical non-linearity at higher filler amounts due to the nano-metric structure and closer particle linkages.     

Experimental investigation and numerical simulation of granite powder filled polymer composites for wind turbine blade: A comparative analysis

This paper describes the mechanical, thermo‐mechanical, and thermal behavior of unfilled E‐glass fiber (10–50 wt%) reinforced polymer (GFRP) composites and granite powder filled (8–24 wt%) GFRP composite in different weight percentages, respectively. The void fraction of unfilled glass epoxy composite is decreased from 7.71% to 3.17% with the increase in fiber loading from 10 to 50 wt%. However, void fraction for granite powder filled GFRP composites show reverse in trend. The granite powder addition in glass‐epoxy composites show significant improvement in hardness (37–47 Hv), impact strength (31.56–37.2 kJ/m²), and stress intensity factor (by 14.29% for crack length of 5 mm) of the composites. The thermo‐mechanical analyses also show strong correlation with the mechanical performance of the composites. The minimum difference of 0.17 GPa in storage and flexural moduli are observed for unfilled 20 wt% glass epoxy composite; whereas, maximum difference of 0.71 GPa is recorded for unfilled 50 wt% glass epoxy composite. Moreover, the numerical and experimentally measured thermal conductivity of unfilled and granite powder filled epoxy composites are within the lower and upper bound values. Hence, a successful attempt is presented for mechanical analysis of full scale model by finite element analysis. The results show that finite element analysis predicted reasonably actual stress value and tip deflection of wind turbine blade. POLYM. COMPOS., 38:1335–1352, 2017. © 2015 Society of Plastics Engineers     

In vitro degradation of poly(l-lactide)/poly(ε-caprolactone) blend reinforced with MWCNTs

The physical and mechanical properties of poly(l-lactide)/poly(??-caprolactone) (PLLA/PCL) blends reinforced with multiwalled carbon nanotubes (MWCNTs) before and after in vitro degradation were investigated. Because of brittleness, PLLA needs to be plasticized by PCL as a soft polymer. The MWCNTs are used to balance the stiffness and the flexibility of PLLA/PCL blends. The results showed that with incremental increase in concentration of MWCNTs in composites, the agglomerate points of MWCNTs were increased. The physical and mechanical properties of prepared PLLA/PCL blends and MWCNT/PLLA/PCL nanocomposites were characterized. The X-ray diffraction analysis of the prepared blends and composites showed that MWCNTs, as heterogeneous nucleation points, increased the lamella size and therefore the crystallinity of PLLA/PCL. The mechanical strength of blends was decreased with incremental increase in PCL weight ratio. The mechanical behavior of composites showed large strain after yielding and high elastic strain characteristics. The tensile tests results showed that the tensile modulus and tensile strength are significantly increased with increasing the concentration of MWCNTs in composites, while, the elongation-at-break was decreased. The in vitro degradation rate of polymer blends in phosphate buffer solution (PBS) increased with higher weight ratio of PCL in the blend. The in vitro degradation rate of nanocomposites in PBS increased about 65% when the concentration of MWCNTs increased up to 3% (by weight). The results showed that the degradation kinetics of nanocomposites for scaffolds can be engineered by varying the contents of MWCNTs.     

Crystallization behavior and mechanical properties of bio‐based green composites based on poly(L‐lactide) and kenaf fiber

Bio‐based polymer composite was successfully fabricated from plant‐derived kenaf fiber (KF) and renewable resource‐based biodegradable polyester, poly(L ‐lactide) (PLLA), by melt‐mixing technique. The effect of the KF weight contents (0, 10, 20, and 30 wt %) on crystallization behavior, composite morphology, mechanical, and dynamic mechanical properties of PLLA/KF composites were investigated. It was found that the incorporation of KF significantly improves the crystallization rate and tensile and storage modulus. The crystallization of PLLA can be completed during the cooling process from the melt at 5°C/min with the addition of 10 wt % KF. It was also observed that the nucleation density increases dramatically and the spherulite size drops greatly in the isothermal crystallization with the presence of KF. In addition, with the incorporation of 30 wt % KF, the half times of isothermal crystallization at 120°C and 140°C were reduced to 46.5% and 28.1% of the pure PLLA, respectively. Moreover, the tensile and storage modulus of the composite are improved by 30% and 28%, respectively, by the reinforcement with 30% KF. Scanning electron microscopy observation also showed that the crystallization rate and mechanical properties could be further improved by optimizing the interfacial interaction and compatibility between the KF and PLLA matrix. Overall, it was concluded that the KF could be the potential and promising filler for PLLA to produce biodegradable composite materials, owing to its good ability to improve the mechanical properties as well as to accelerate the crystallization of PLLA. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Development of degradable polymer composites from starch and poly(ethyl cyanoacrylate)

This report describes the development of degradable polymer composites, which can be made at room temperature without special equipment. The developed composites are made from poly(ethyl cyanoacrylate) and starch. Ethyl cyanoacrylate monomers are mixed with starch and the polymerization reaction of these monomers was initiated by dissociated OH^‐ ions from moisture on the surface of the starch. After the polymerization, the body of starch granules acts as filler and the micrometer‐scale gaps formed by starch granules are filled with the poly(ethyl cyanoacrylate). The glass transition temperature of the composite matrix ranges from 106°C to 113°C and thermal degradation begins around 160°C. The polymer composites produced by this procedure contain 50–64 wt% of starch and have compressive strengths of 80 (±10) MPa. Optimum starch composition for these composites is ∼60 wt%. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Selective interfacial localization in conducting polycaprolactam/ethylene vinyl acetate/carbon black composites

Unusual electrical conductivity was demonstrated by ethylene vinyl acetate/polycaprolactam/carbon black (CB) composites. The critical exponent value was 1.2 ± 0.2 for ternary composites and was greater than 2.0 for the binary composites, indicating two‐dimensional electrical conduction in ternary composites. The ternary composites also showed inverted U‐shaped conductivity curves when CB weight fraction was greater than 10 wt%. However, at 10 wt% CB, a discontinuous conductivity curve showing conductivity only when polycaprolactam content was greater than 50% was observed, suggesting substantial variation in the interfacial characteristics with the change in the blend composition. Small‐angle X‐ray scattering studies pointed out that ternary composites can be viewed as a two‐phase system with sharp boundaries, and that interface layer in the composites does not exist. Differential scanning calorimetry studies suggested composition dependent variation in the crystallinity of polycaprolactam phase, partially contributing to the increase in the composites' conductivity at higher polycaprolactam fractions. POLYM. COMPOS., 34:912–919, 2013. © 2013 Society of Plastics Engineers     

Electron transport properties of polyaniline composite films containing poly(3‐hydroxybutyric acid)

Polyaniline (PANI) composites containing poly(3‐hydroxybutyric acid) (PHB) were synthesized via in situ deposition technique. The oxidative polymerization of aniline hydrochloride was carried out by dissolving different weight percentages (10 wt%, 20 wt%, 30 wt%, 40 wt%, and 50 wt%) of PHB using ammonium persulfate as an oxidant. The as‐synthesized composites were characterized using Fourier‐transform infrared spectroscopy and X‐ray diffraction pattern. The surface morphology of the resulting composites was studied using transmission electron microscopy. The temperature‐dependent direct current conductivity of the synthesized composite films was measured, and the activation energy responsible for the conductivity was examined. Incorporation of the biodegradable polymer, PHB, during the preparation of new PANI composites significantly increased the conductivity of the resulting composites. POLYM. COMPOS., 34:1655–1662, 2013. © 2013 Society of Plastics Engineers     

Poly(butylene succinate)‐based biocomposites filled with polysaccharide nanocrystals: Structure and properties

In this work, two polysaccharide nanocrystals‐rod‐like cellulose whisker (CW) and platelet‐like starch nanocrystal (SN) were individually incorporated into an aliphatic thermoplastic polyester to produce biodegradable poly(butylene succinate) (PBS)/nanocrystals biocomposites. At loading levels of 2 wt% CW or 5 wt% SN the PBS‐based nanocomposites showed simultaneous enhancement of strength and elongation compared to the neat PBS. This was primarily attributed to the uniform dispersion of nanofillers and strong interfacial adhesion between filler and matrix. Nucleation of the nanocrystals, formation of a percolating network, and interaction between filler and matrix collectively contributed to the improvement of crystallinity and thermal properties of the composites. This high performance, fully biodegradable, eco‐friendly nanocomposite will expand the utilization of polysaccharide nanocrystals from renewable bioresources and the practical application of PBS. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Utilization of linseed cake as a postagricultural functional filler for poly(lactic acid) green composites

Linseed cake (LC), a byproduct of linseed oil extraction, is used as a functional filler for production of biodegradable composites. To determine the influence of residual linseed crude oil contained in lignocellulosic filler on the properties of the poly(lactic acid) (PLA)-based composites with 5–30% filler content, two types of LC were analyzed: a defatted and an unmodified one. Complex analysis of the composites' properties change was conducted in relation to their structure modification caused by the addition of a waste filler. It was found that the addition of LC resulted in simultaneous plasticization and improved crystallization of PLA. Lignocellulosic particles and crude linseed oil contained in the LC powder provided a modifying effect, influencing the level of crystallinity and mechanical and thermomechanical properties. Using LC may thus overcome one of the main drawbacks of PLA, which is brittleness and low crystallinity. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47152.     

Characterization of modulus and glass transition phenomena in poly(L‐lactide)/hydroxyapatite composites

In order to study the dynamic‐mechanical properties of Poly(L‐lactide)/Hydroxyapatite (PLLA/HA) composites, two different molecular weight (inherent viscosity (η_inh): 4.0 (dL/g), and 7.8 (dL/g)) poly(L‐lactide) (PLLA) were synthesized by bulk polymerization and filled with 10%, 30%, and 50% (w/w) with medical grade HA (size range: 25–45 μm and Ca/P = 1.69). The plain PLLA polymers and PLLA/HA composites were compression molded and machined to yield 50 × 3 × 2 mm³ specimens. The composites were investigated by dynamic mechanical thermal analyzer (DMTA) of imposed bending load on rectangular specimens over a temperature range from 30 to 120°C using multiple frequencies (0.3–50 Hz). The results showed that the bending storage modulus (E′) of the composites increased linearly with the percentage of the filler, reaching at 37°C and 0.1 Hz about 2.5, 3.7 and 5.0 GPa with 10, 30 and 50% of HA respectively. The glass transition temperature, evaluated at the tan δ peaks, were in the range 70–80°C and 50–70°C for PLLA matrix and PLLA composites respectively. The activation energies at the glass transition temperature were calculated from the Arrhenius plot in the range of 102–111 Kcal/mol for the composites, whereas 132 and 148 Kcal/mol were found for low and high molecular weight of PLLA respectively. The content of amorphous phase was evaluated from the intensity of tan δ peak. Results showed that HA causes an amorphous phase with a greater mobility with respect to the pure PLLA.     

Porous biodegradable polyester blends of poly(L‐lactic acid) and poly(ε‐caprolactone): physical properties,morphology, and biodegradation

Poly(L ‐lactic acid) (PLLA), poly(ε‐caprolactone) (PCL), and their films without or blended with 50 wt% poly(ethylene glycol) (PEG) were prepared by solution casting. Porous films were obtained by water‐extraction of PEG from solution‐cast phase‐separated PLLA‐blend‐PCL‐blend‐PEG films. The effects of PLLA/PCL ratio on the morphology of the porous films and the effects of PLLA/PCL ratio and pores on the physical properties and biodegradability of the films were investigated. The pore size of the blend films decreased with increasing PLLA/PCL ratio. Polymer blending and pore formation gave biodegradable PLLA‐blend‐PCL materials with a wide variety of tensile properties with Young's modulus in the range of 0.07–1.4 GPa and elongation at break in the range 3–380%. Pore formation markedly increased the PLLA crystallinity of porous films, except for low PLLA/PCL ratio. Polymer blending as well as pore formation enhanced the enzymatic degradation of biodegradable polyester blends. Copyright © 2006 Society of Chemical Industry