PHBV Blends Research Articles

The effect of additives on the biodegradation of polyhydroxyalkanoate (PHA) in marine field trials

The persistence of conventional fossil fuel-derived plastics in marine ecosystems has raised significant environmental concerns. Biodegradable plastics are being explored as an alternative. This study investigates the biodegradation behaviour in two marine environments of melt-extruded sheets of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) bioplastic as well as blends of PHBV with a non-toxic plasticiser (triethyl citrate, TEC) and composites of PHBV with wood flour. Samples were submerged for up to 35 weeks in two subtropical marine conditions: on the sandy seabed in the sublittoral benthic zone and the sandy seabed of an open air mesocosm with pumped seawater. Rates of biodegradation, lag times and times to 95 % mass loss (T95) were determined through mass loss data and Gompertz modelling. Mechanisms of biodegradation were studied through changes in molecular weight, mechanical properties and surface features. Results reveal a rapid biodegradation rate for all PHBV samples, demonstrating a range of specific biodegradation rates relative to exposed surface area of 0.03 ± 0.01 to 0.09 ± 0.04 mg.d−1.cm−2. This rapid rate of biodegradation meant that the subtle variations in biodegradation mechanisms across different sample thicknesses and additive compositions had little effect on overall lifetimes, with the T95 for most samples being around 250–350 days, regardless of site, highlighting the robust biodegradability of PHBV in seawater. It was only the PHBV-wood flour composite that showed faster biodegradation, and that was only in the exposed ocean site. The mesocosm site was otherwise shown to be a good model for the open ocean, with very comparable biodegradation rates and changes in mechanical properties over time.

Influence of different dimensional nanoparticles on the properties of poly(β-hydroxybutyrate-co-valerate) nanocomposites

Abstract In order to study the effect of nanoparticle dimensions on the thermodynamic properties of PHBV and PHBV blends, one-dimensional cellulose nanocrystals (CNC), two-dimensional graphene, and zero-dimensional hydrophobic nano-silica were selected to regulate the crystallization and mechanical properties of poly(β-hydroxybutyrate-co-valerate) (PHBV) and PHBV blends. The morphology, crystallization process, mechanical property and rheological response of PHBV nanomaterials were analyzed. Experimental results show that the three selected nanomaterials all hinder the crystallization process of PHBV, among which two-dimensional graphene exhibits the most obvious hindrance. At the same time, two-dimensional graphene can improve the tensile strength and impact strength of PHBV. However, in the rheological response of PHBV nanocomposites, zero-dimensional hydrophobic nano-silica and one-dimensional cellulose nanocrystals show more obvious regulatory effects than two-dimensional graphene.

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Blends with Poly(caprolactone) and Poly(lactic acid): A Comparative Study.

Poly(hydroxybutyrate-co-hidroxyvalerate) (PHBV) is a biodegradable polymer, which is a potential substitute for plastics made from fossil resources. Due to its practical interest in the field of tissue engineering, packaging, sensors, and electronic devices, the demand for PHBV with specific thermal, electrical, as well as mechanical requirements is growing. In order to improve these properties, we have developed PHBV blends with two thermoplastic biodegradable polyesters, including poly(caprolactone) (PCL) and poly(lactic acid) (PLA). We analysed the effect of these biopolymers on the morphological, wetting, structural, thermal, mechanical, and electrical characteristics of the materials. Further, the biodegradation of the samples in simulated body fluid conditions was evaluated, as well as the antibacterial activity. The results demonstrate that the blending with PCL and PLA leads to films with a dense morphology, increases the hydrophilic character, and induces a reinforcement of the mechanical characteristics with respect to pristine PHBV. In addition, a decrease in dielectric constant and a.c. electrical conductivity was noticed for PHBV/PLA and PHBV/PCL blends compared to neat PHBV polymer. All neat polymers and blends showed antibacterial properties against S. aureus, with more than 40% bacterial reduction, which increased to 72% in the presence of PCL polymer for a blend ratio of 50/50. Thus, it is demonstrated a suitable way to further tailor a variety of functionalities of PHBV for specific applications, by the development of polymer blends with PLA or PCL.

Air-jet spun PHBV/PCL blend tissue engineering scaffolds exhibit improved mechanical properties and cell proliferation

This study aimed to optimize the preparation parameters for air-jet spun blended poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and polycaprolactone (PCL) submicron fibrous scaffolds. Blends of PHBV and PCL were made using different weight ratios of polymers and examined for their mechanical, morphological, and biological properties. The 50/50 ratio PHBV/PCL blend scaffolds showed better overall mechanical properties compared to the scaffolds with higher PHBV content and provided better cell attachment and proliferation compared to PCL scaffolds. The incorporation of PCL improved the degree of crystallinity, thermal stability, and mechanical properties of PHBV/PCL blend scaffolds. In vivo subcutaneous implantation and subsequent histological analysis of the implanted scaffolds indicated that the scaffolds were compatible with animal tissues. The findings show that air-jet spun PHBV/PCL blended scaffolds in a 50/50 ratio can be employed in many tissue engineering applications.

Bio-Polyester/Rubber Compounds: Fabrication, Characterization, and Biodegradation.

Biobased and biodegradable polymers (BBDs) such as poly(3-hydroxy-butyrate), PHB, and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) are considered attractive alternatives to fossil-based plastic materials since they are more environmentally friendly. One major problem with these compounds is their high crystallinity and brittleness. In order to generate softer materials without using fossil-based plasticizers, the suitability of natural rubber (NR) as an impact modifier was investigated in PHBV blends. Mixtures with varying proportions of NR and PHBV were generated, and samples were prepared by mechanical mixing (roll mixer and/or internal mixer) and cured by radical C-C crosslinking. The obtained specimens were investigated with respect to their chemical and physical characteristics, applying a variety of different methods such as size exclusion chromatography, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermal analysis, XRD, and mechanical testing. Our results clearly indicate that NR-PHBV blends exhibit excellent material characteristics including high elasticity and durability. Additionally, biodegradability was tested by applying heterologously produced and purified depolymerases. pH shift assays and morphology analyses of the surface of depolymerase-treated NR-PHBV through electron scanning microscopy confirmed the enzymatic degradation of PHBV. Altogether, we prove that NR is highly suitable to substitute fossil-based plasticizers; NR-PHBV blends are biodegradable and, hence, should be considered as interesting materials for a great number of applications.

Thermal pre-processing before extraction of polyhydroxyalkanoates for molecular weight quality control

Past studies have repeatedly demonstrated the technical feasibility to produce polyhydroxyalkanoate (PHA) using bacterial biomass of mixed microbial cultures (MMCs). Commercial quality grades of poly(3-hydroxybutyrate-co-3-hydroxyvalerate), PHBV, can be produced with control of average monomer composition. However, demonstration of PHBV production and recovery with quality control of molecular weight (MW) distribution has been lacking in the research literature. Towards this goal, a workflow has been developed for characterizing molecular weight control by thermal treatment pre-processing of dried PHA-rich biomass before solvent extraction. Dimethyl carbonate (DMC) was a suitable solvent in this workflow in the routine evaluation of extractable PHA. From assessments of DMC extraction using differential scanning calorimetry, 125 °C was selected for nominally 100 percent extraction yield independent of polymer 3-hydroxyvalerate (3HV) content (2 to 41 wt.% 3HV) and molecular weight (100 to 1400 kDa). Intrinsic viscosity measurements of PHBV in DMC at 60 °C was used for molecular weight monitoring. Mark-Houwink constants, α (0.738 ± 0.010) and LogK (-2.016 ± 0.025), were estimated for a PHBV co-polymer blend having 36 wt.% 3HV. A model of random scission supported that weight average molecular weight (Mw) was a more robust metric, compared to number average molecular weight (Mn), for assessing the polymer scission rates. During isothermal heat treatment for a given biomass batch, interpreted scission rate was reproducible and commonly, but not always, constant in time. Scission rates between biomass batches were also variable. Measured properties of the polymer in the biomass (thermal stability, biomass PHA content, PHBV grade, initial moisture content) could not be correlated to this observed batch-to-batch variation of scission rate. Molecular weight loss before extraction did not influence the melting temperatures of the co-polymer blends of PHBV evaluated over a wide sub-eutectic range of average 3HV content. Molecular weight changes for these PHBV co-polymer blends were considered to have likely influenced the nature of blend 3HV distribution, and consequently, crystallization behaviour. Molecular weight loss effects on crystallization behaviour at constant PHBV average 3HV wt.% content could then have contributed to the observed variability for glass transition temperatures and melting enthalpies. However, a reproducible correlation between this variability and MW change was not observed.

Monolayer films from poly(lactic acid) PLA/poly(3-hydroxybutyrate-co-hydroxyvalerate) PHBV blends for food packaging applications

Monolayer films from poly(lactic acid) PLA/poly(3-hydroxybutyrate-co-hydroxyvalerate) PHBV blends for food packaging applications

Effects of Endic Anhydride Grafted PPC on the Properties of PHBV Blends.

Poly(β-hydroxybutyrate-co-β-hydroxyvalerate) (PHBV) was modified with endic anhydride grafted poly(propylene carbonate) (EA–PPC), and then PHBV/EA–PPC composite polymers were prepared by melt blending under the catalysis of stannous octoate (Sn(Oct)2). The blends were characterized by an electronic universal testing machine, cantilever impact testing machine, and differential scanning calorimeter (DSC), as well as dynamic mechanical analysis (DMA) and field emission scanning electron microscopy (FESEM). Effects of the amount of Sn(Oct)2 on the mechanical properties, thermal properties, and morphology of the blends were discussed. The results showed that the addition of Sn(Oct)2 promoted the transesterification reaction between PHBV and EA–PPC, and the compatibility between PHBV and PPC was greatly improved. When the amount of Sn(Oct)2 was 3 wt%, the impact strength and elongation at break of the PHBV/EA–PPC blend increased from 3.7 kJ/m2 and 4.1% to 5.9 kJ/m2 and 387.5%, respectively, and there was no significant decrease in tensile strength. Additionally, four esterification reaction mechanisms for PHBV/EA–PPC blends were proposed.

Development and Characterization of Fully Renewable and Biodegradable Polyhydroxyalkanoate Blends with Improved Thermoformability.

Poly(3-hydroxybutyrate-co-3-valerate) (PHBV), being one of the most studied and commercially available polyhydroxyalkanoates (PHAs), presents an intrinsic brittleness and narrow processing window that currently hinders its use in several plastic applications. The aim of this study was to develop a biodegradable PHA-based blend by combining PHBV with poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH), another copolyester of the PHA family that shows a more ductile behavior. Blends of PHBV with 20% wt., 30% wt., and 40% wt. of PHBH were obtained by melt mixing, processed by cast extrusion in the form of films, and characterized in terms of their morphology, crystallization behavior, thermal stability, mechanical properties, and thermoformability. Full miscibility of both biopolymers was observed in the amorphous phase due to the presence of a single delta peak, ranging from 4.5 °C to 13.7 °C. Moreover, the incorporation of PHBH hindered the crystallization process of PHBV by decreasing the spherulite growth rate from 1.0 µm/min to 0.3 µm/min. However, for the entire composition range studied, the high brittleness of the resulting materials remained since the presence of PHBH did not prevent the PHBV crystalline phase from governing the mechanical behavior of the blend. Interestingly, the addition of PHBH greatly improved the thermoformability by widening the processing window of PHBV by 7 s, as a result of the increase in the melt strength of the blends even for the lowest PHBH content.

Development of green materials from ENR-25/PHBV blends: Curing characteristics and mechanical performance

The objective of this work was to develop green materials from epoxidized natural rubber (25% epoxidation), (ENR-25), poly(3-hydroxybutyrate-co-3-hydroxyvalerate), (PHBV), and polybutadiene adducted with maleic anhydride, (PB-g-MA) as compatibilizer. The ENR-25/PHBV blends were prepared at the ratio of 100/0, 90/10, and 80/20 with 0 and 10 %wt. PB-g-MA. The blends were prepared using an internal mixer, where PHBV was first melted at a temperature of 175 °C before mixing with ENR-25 and the incorporation of a compatibilizer. The mixing of ENR-25 and PHBV was continued at a temperature of 175 °C and mixing speed of 50 rpm until it reaches the complete blending time. All ENR-25/PHBV blends were then mixed with curing agents in an internal mixer at a temperature of 50 °C. The cure characteristics were determined using a moving die rheometer (MDR). Then vulcanization proceeded in a compression molding machine. The result shows that the addition of PHBV enhanced the modulus of ENR-25 for every blend ratio with and without compatibilizer owing to the mechanical properties of PHBV. Significantly, the PB-g-MA compatibilizer successfully improved the interface adhesion between ENR-25 and PHBV and the decrease in phase size was clearly seen in the SEM images.

Osteogenic differentiation of rat bone mesenchymal stem cells cultured on poly (hydroxybutyrate-co-hydroxyvalerate), poly (\u03b5-caprolactone) scaffolds

Bioresorbable biomaterials can fill bone defects and act as temporary scaffold to recruit MSCs to stimulate their differentiation. Among the different bioresorbable polymers studied, this work focuses on poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) and poly(ε-caprolactone) (PCL). Were prepared blends of PHBV and PCL to obtain PHBV based biomaterials with good tenacity, important for bone tissue repair, associated with biocompatible properties of PCL. This study assesses the viability of Vero cells on scaffolds of PHBV, PCL, and their blends and the osteogenic differentiation of mesenchymal stem cells (MSCs). Materials were characterized in surface morphology, DSC and Impact Strength (IS). Vero cells and MSCs were assessed by MTT assay, cytochemical and SEM analysis. MSC osteogenic differentiation was evaluated through alizarin red staining and ALP activity. We found some roughness onto surface materials. DSC showed that the blends presented two distinct melting peaks, characteristic of immiscible blends. IS test confirmed that PHBV-PCL blends is an alternative for increase the tenacity of PHBV. MTT assay showed cells with high metabolic activities on extract toxicity test, but with low activity in the direct contact test. SEM analysis showed spreading cells with irregular and flattened morphology on different substrates. Cytochemical study revealed that MSCs maintained their morphology, although in smaller number for MSCs. The development of nodules of mineralized organic matrix in MSC cultures was identified by alizarin red staining and osteogenic differentiation was confirmed by the quantification of ALP activity. Thus, our scaffolds did not interfere on viability of Vero cells or the osteogenic differentiation of MSCs.

Thermal and Rheological Behavior of Binary Blends of Poly(hydroxybutyrate‐co‐hydroxyvalerate) and Poly(ethylene‐co‐vinyl acetate) with Different Vinyl Acetate Content

The aim of this study is to investigate the influence of vinyl acetate (VA) content on the thermal and rheological properties of poly(hydroxybutyrate‐co‐hydroxyvalerate) (PHBV)/poly(ethylene‐co‐vinyl acetate) (EVA) blends. Binary blends of PHBV and EVA containing 65 wt% (EVA65) and 90 wt% (EVA90) VA were prepared by torque rheometry and their thermal properties were studied by differential scanning calorimetry (DSC). Rheograms of PHBV/EVA65 containing up to 40 wt% EVA showed that the torque values decrease as a function of mixing time due to the thermo‐mechanical degradation, which preferentially for PHBV is chain scission. The increase in the EVA65 concentration results in torque stability probably due to the balance between chain scission of the PHBV and chain branching of the EVA65. For PHBV/EVA90 blends, the torque values are stable indicating that the presence of EVA90 decreases the degradation process of the PHBV and hence increases the thermal stability of blends. DSC curves showed that the PHBV cold crystallization temperature (Tcc) increased and cold crystallization (ΔHcc) and melting enthalpies (ΔHm) decreased with the increase in the EVA content, independently of VA content and blend morphology. DSC curves of PHBV/EVA65 showed two glass transition temperatures and clear phase separations, in all studied formulations, typical of immiscible systems. In contrast to it, PHBV/EVA90 blends showed a single glass transition, suggesting total miscibility. Both findings were corroborated by scanning electron microscopy (SEM) analysis.

Partial and Complete Wetting in Ultralow Interfacial Tension Multiphase Blends with Polylactide.

The control of phase structuring in multiphase blends of polylactide (PLA) with other polymers is a viable approach to promote its broader implementation. In this article, ternary and quaternary blends of PLA with poly(butylene succinate) (PBS), poly(butylene adipate-co-terephthalate) (PBAT), and poly(3-hydroxybutyrate-co-hydroxyvalerate) (PHBV) are prepared by melt blending. The interfacial tensions between components are measured using three different techniques, and a Fourier transform infrared imaging technique is developed for the purpose of unambiguous phase identification. A tricontinuous complete wetting behavior is observed for the ternary 33PLA/33PBS/33PBAT blend before and after quiescent annealing, which correlates closely with spreading theory analysis. In the quaternary PLA/PBS/PBAT/PHBV blend, a concentration-dependent wetting behavior is found. At 10 vol % PBAT, self-assembled partially wet droplets of PBAT are observed at the interface of PBS and PHBV, and they remain stable after quiescent annealing as predicted by spreading theory. In contrast, at 25 vol % PBAT, a quadruple continuous system is observed after mixing, which only transforms to partially wet PBAT droplets after subsequent annealing. These results clearly indicate the potential of composition control during the mixing of multiphase systems to result in a complete change of spreading behavior.

Toughness Enhancement of Commercial Poly (Hydroxybutyrate-co-Valerate) (PHBV) by Blending with a Thermoplastic Polyurethane (TPU)

Poly(hydroxyl butyrate-co-valerate) (PHBV) is a biopolymer synthesized by microorganisms that is fully biodegradable with improved thermal and tensile properties with respect to some commodity plastics. However, it presents an intrinsic brittleness that limits its potential application in replacing plastics in packaging applications. Films made of blends of PHBV with different contents of thermoplastic polyurethane (TPU) were prepared by single screw extruder and their fracture toughness behavior was assessed by means of the essential work of fracture (EWF) Method. As the crack propagation was not always stable, a partition method has been used to compare all formulations and to relate results with the morphology of the blends. Indeed, fully characterization of the different PHBV/TPU blends showed that PHBV was incompatible with TPU. The blends showed an improvement of the toughness fracture, finding a maximum with intermediate TPU contents.

Blending Modification of PHBV/PCL and its Biodegradation by Pseudomonas mendocina

Poly(3-hydroxybutyrate-co-hydroxyvalerate) (PHBV) is a biodegradable polymer synthesized in microorganisms. The application of PHBV is limited by certain material disadvantages. Poly(e-caprolactone) (PCL) possesses excellent thermodynamic and mechanical properties and was used to modify PHBV in the presence of triethyl citrate (TEC) and dicumyl peroxide (DCP), which was used as plasticizer and grafting agent, respectively. The effects of PCL and additive agents on the mechanical, thermal, amphipathic and degradability behaviors of the blends were investigated. The results showed that the mechanical properties of the PHBV blends improved by PCL incorporation and improved even further after TEC and DCP addition. The addition of DCP could not induce an increase in crystallization temperature but improved the crystallization degree of the blends. The presence of hydrophilic groups in TEC leads to an apparent increases in the hydrophilicity of the PHBV blends. A PHBV/PCL blend (40/60) with TEC (20 wt.%) and DCP (0.5 wt.%) was chosen for its good mechanical properties and hydrophilicity. The chosen ratio of the blends was also shown a preferable degradation activity by biodegradation assay using Pseudomonas mendocina. The addition of TEC and DCP has no conspicuous negative effect on the biodegradation.

Denitrification of groundwater using PHBV blends in packed bed reactors and the microbial diversity

In the present study, three kinds of biopolymers, PHBV, PHBV/starch and PHBV/bamboo powder (BP) blends were used as carbon source and biofilm carriers for denitrification in packed bed reactors to remove nitrate from groundwater. Results showed that a fast start-up was obtained in bioreactors filled with both PHBV/Starch and PHBV/BP blends without external inocula and it took more than 3 month for PHBV reactor to reach the same loading rate. The PHBV/BP packed reactor exhibited a better nitrate removal efficiency (87.4 ± 7.0%) and less adverse effects in nitrite accumulation and DOC release (below 0.5 mg NO2N L−1 and 10.5 mg DOC L−1 in the effluent) during stable operation. Pyrosequencing analysis demonstrated that bacteria belonging to genus Clostridium in phylum Firmicus, which play the primary role in degrading the biopolymers, are the most dominant (33–15% of the sequences). The predominant species in all samples is related to Clostridium crotonatovorans. All the identified 11 genera of denitrifying bacteria affiliated with phylum Proteobacteria and constituted 30–55% in the representative sequences. The PHBV/BP blend is economically attractive carbon source with good denitrification performance.

Mechanical and Thermal Behavior of Blends of Poly(hydroxybutyrate-co-hydroxyvalerate) with Ethylene Vinyl Acetate Copolymer

Ethylene vinyl acetate copolymer (EVA), with vinyl acetate contents of 60% or 80%, was used to improve the mechanical properties of poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV). Blends of PHBV/EVA were prepared with the ratios of 90:10, 70:30, and 50:50. Stress–strain results indicated that the tensile strength, elongation at break, Young's modulus, and toughness of PHBV blends could be adjusted by changing the composition of blends and miscibility. It was found that high elongation at break, ca. 200%, was obtained for PHBV/EVA80 (50:50).

Crystallization and melting behavior of partially miscible six‐armed poly(l‐lactic acid)/poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) blends

ABSTRACTThe crystallization kinetics and spherulitic morphology of six‐armed poly(L‐lactic acid) (6a‐PLLA)/poly(3‐hydroxybutyrate‐co−3‐hydroxyvalerate) (PHBV) crystalline/crystalline partially miscible blends were investigated with differential scanning calorimetry and polarized optical microscopy in this study. Avrami analysis was used to describe the isothermal crystallization process of the neat polymers and their blends. The results suggest that blending had a complex influence on the crystallization rate of the two components during the isothermal crystallization process. Also, the crystallization mechanism of these blends was different from that of the neat polymers. The melting behavior of these blends was also studied after crystallization at various crystallization temperatures. The crystallization of PHBV at 125°C was difficult, so no melting peaks were found. However, it was interesting to find a weak melting peak, which arose from the PHBV component for the 20/80 6a‐PLLA/PHBV blend after crystallization at 125°C, and it is discussed in detail. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 42548.

Film blowing of PHBV blends and PHBV‐based multilayers for the production of biodegradable packages

ABSTRACTPoly(hydroxy butyrate‐co‐valerate) (PHBV) is a biodegradable polymer that is difficult to melt process into films. Such difficulty is mirrored in the lack of literature on film blowing of PHBV‐ or PHBV‐based materials. To circumvent this problem, 70/30 wt % blends of PHBV with a biodegradable compound (PBSebT), or with poly(butylene adipate‐co‐terephtalate) (PBAT), were prepared and tested for extrusion film blowing. Both blends showed a similar rheological pattern at 175°C, which is the maximum processing temperature with tolerable thermal degradation. Blending stabilized the film bubbles, thus widening the processing window. However, film properties such as tensile modulus, strain at break and tear resistance remained isotropic and crystallinity characteristics in the machine and transverse directions were generally similar. To bypass the thermal degradation associated with polymer blending, PHBV/PBAT films were coextruded. These showed enhanced functional properties when compared with films blown from blends. The mechanical properties of bilayered films matched those of films blown from commercial PBAT designed for food packaging. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 42165.

Preparation, thermal properties, and morphology of graft copolymers in reactive blends of PHBV and PPC

AbstractChemical modification of poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) with glycidyl methacrylate (GMA) monomer, followed by reactively blending with end‐capped poly(propylene carbonate) (PPC) (50 wt%) was carried out during melt processing with dicumyl peroxide (DCP) initiation. The two kinds of graft copolymers of PHBV‐g‐GMA and PHBV‐g‐PPC were extracted with Soxhlet's apparatus, respectively. These grafting reaction mechanisms were proposed and the presence of grafting copolymers was confirmed by weight analysis, FTIR and NMR. The methyne carbon of GMA is confirmed to attach to quaternary carbon of the PHBV backbone. The epoxy groups in the copolymer of PHBV‐g‐GMA were capable to react with the carboxyl groups of end‐capped PPC, resulting in the formation of PHBV‐g‐PPC copolymer in situ. Their thermal properties and morphology were also characterized by DSC, WAXD, POM, and AFM. It revealed that after GMA grafting, the degradation of PHBV decreased and the nucleation of PHBV improved. The crystallinity degree, spherulites dimension and phase segregation between the two macromolecules decreased after PHBV grafted with PPC. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers