Reactive compatibilization has been widely applied to enhance the compatibility of polymer blends,thereby improving their mechanical properties.However,it generally reduces the chain mobility and regularity,often lead...Reactive compatibilization has been widely applied to enhance the compatibility of polymer blends,thereby improving their mechanical properties.However,it generally reduces the chain mobility and regularity,often leading to slower polymer crystallization.Here,we demonstrate that reactive compatibilization in poly(lactic acid)/poly(butylene adipate-co-terephthalate)(PLA/PBAT)blends unexpectedly promotes PLA matrix crystallization during injection molding,in contrast to the retarded kinetics observed in differential scanning calorimetry isothermal crystallization studies.The phase morphology,rheological behavior,and crystalline structure were systematically analyzed to elucidate markedly different crystallization kinetics under static and shear fields.The potential mechanism underlying crystallization enhancement is attributed to PBAT domain refinement and viscosity increase induced by reactive compatibilization,which,under shear flow,create favorable conditions for crystallization by enhancing PBAT fibril nucleation and retarding the relaxation of oriented PLA chains.This study offers new perspectives on the effect of reactive compatibilization on the polymer crystallization behavior.展开更多
In-situ reactive compatibilization of high-density polyethylene （HDPE）/ground tire rubber （GTR） blends by dicumyl peroxide （DCP） and HY-2045 - a kind of thermoplastic phenolic resin without catalyst was inves...In-situ reactive compatibilization of high-density polyethylene （HDPE）/ground tire rubber （GTR） blends by dicumyl peroxide （DCP） and HY-2045 - a kind of thermoplastic phenolic resin without catalyst was investigated by studying the mor-phology, stress and strain behavior, dynamic mechanical properties and crystallization performance of the blends. Scanning e-lectron microscopy （SEM） results show that there are a lot of fibrous materials distributing in the interface, which connects the dispersed phase with the matrix and obtains better interfacial strength for prominent mechanical properties. The addition of compatibilizers results in the decrease of crystallinity of the blends and the disappearance of an obvious yield phenomenon, which was proved by the differential scanning calorimeter （DSC） test and X-ray diffraction （XRD） characterization Although the crystallinity of the blends decreases,the tensile strength and tensile strain of the blends significantly increases, especially for the HDPE/GTR/DCP/HY-2045 blends, which is possibly attributed to the good compatibility of the blends owing to the in-situ interface crosslinking. In addition, it is found that the compatibilizing HDPE/GTR blends shows a higher tan^ peak temperature and a broaden transition peak for GTR phase.展开更多
The influences of hyperbranched polyethylenimine （hPEI）, which possesses many reactive amino end-groups, on the blending properties of bisphenol-A polycarbonate （PC） and amorphous polyamide （aPA） were systematic...The influences of hyperbranched polyethylenimine （hPEI）, which possesses many reactive amino end-groups, on the blending properties of bisphenol-A polycarbonate （PC） and amorphous polyamide （aPA） were systematically investigated. Scanning electron microscopy （SEM） and differential scanning calorimetry （DSC） were used to observe the effect of hPE1 on morphologies of PC and aPA phases in bulk blends. While the interfacial fracture toughness between planar PC and aPA layers with and without hPEI was studied by using augmented double cantilever beam （ADCB） method. Results show that the compatibility in PC/aPA blends can be significantly improved by adding a small amount of hPEI, mainly due to the interchange reactions between the polymers leading to the formation of block copolymers, cross-linked polymers and molecules with other constitutions. The augmented double cantilever beam experiments showed that the reactive process drastically reinforced the interfacial adhesion between planar layers of PC and aPA. However, degradation takes place during annealing at 180℃, which was responsible for the production of small molar mass species of PC.展开更多
Melt blending of biodegradable polyesters such as poly(lactic acid)(PLA)and poly(butylene adipate co-terephthalate)(PBAT)with a compatibilizer and natural filler offers a chance to develop biodegradable biocomposites ...Melt blending of biodegradable polyesters such as poly(lactic acid)(PLA)and poly(butylene adipate co-terephthalate)(PBAT)with a compatibilizer and natural filler offers a chance to develop biodegradable biocomposites with improved performance.In this study,we examined how PLA/PBAT blends behave during ultimate biodegradation(mineralization),both with and without compatibilizer and algae as a reinforcement,under controlled composting conditions using carbon dioxide(CO_(2))respirometry techniques.Throughout the biodegradation process,the disintegration behaviour,thermal,chemical,and morphological properties of test samples before and after biodegradation were analyzed using FTIR,TGA,DSC,and SEM techniques.The results from CO_(2)biodegradation showed that PLA/PBAT blend exhibits a higher rate of biodegradation compared to neat PLA and PBAT.The addition of algae to a compatibilized PLA/PBAT blend showed an enhanced biodegradation rate due to hydrolytic cleavage and microbial assimilation.This was further supported by the disintegration test,where algae-reinforced composites showed fragmentation within 30 days.FTIR,TGA and SEM analysis revealed the structural changes that occurred during biodegradation,highlighting the role of algae in affecting the thermal stability and surface morphology.After the compost biodegradation step,eco-toxicity seed germination was conducted on the test samples.Plant seed germination test results confirmed that all test samples achieved maximumgermination.This indicates there were no toxic residues,suggesting that the degraded materials are environmentally safe.Overall,this study contributes to the understanding of biodegradation mechanisms and the ecological impact of bio-based polymer composites as eco-friendly materials and products.展开更多
Polylactide(PLA)films blended with poly(butylene adipate-co-terephthalate)(PBAT)were hot melted using a twin screw extruder with the addition of triethyl citrate(TEC)as a plasticizer and toluene diisocyanate(TDI)as a ...Polylactide(PLA)films blended with poly(butylene adipate-co-terephthalate)(PBAT)were hot melted using a twin screw extruder with the addition of triethyl citrate(TEC)as a plasticizer and toluene diisocyanate(TDI)as a compatibilizer.The synergistic effects of the two additives on the mechanical,thermal,and morphological properties of the PLA/PBAT blend films were investigated.The influence of TEC content on the plasticized PLA films and the effect of TDI’s presence on the PLA/PBAT blend films were also studied by comparing them with neat PLA.The results showed a pronounced increase in elongation at break of the plasticized PLA films with increasing TEC levels,but a slight reduction in thermal stability.Also,the addition of TEC and TDI to the blend system not only synergistically enhanced the tensile properties and tensile-impact strength of the PLA/PBAT blends,but also affected their crystallinity and cold crystallization rate,a result of the improvement of interfacial interaction between PLA and PBAT,including the enhancement of their chain mobility.The synergy of the plasticization and compatibilization processes led to the improvement of tensile properties,tensile-impact strength,and compatibility of the blends,accelerating cold crystallization without affecting crystallization.展开更多
Polylactide （PLA） films blended with 10 wt% poly（butylene adipate-co-terephthalate） （PBAT） were prepared by using a twin screw extruder in the presence of the nucleating agent of titanium dioxide （TiO2） and th...Polylactide （PLA） films blended with 10 wt% poly（butylene adipate-co-terephthalate） （PBAT） were prepared by using a twin screw extruder in the presence of the nucleating agent of titanium dioxide （TiO2） and the compatibilizers of toluene diisocyanate （TDI） and PLA-grafted-maleic anhydride （PLA-g-MA）. The synergistic effect of the nucleation and compatibilization on the properties and crystallization behavior of the PLA/PBAT （PLB） films was explored. The results showed that the addition of TiO2 significantly enhanced the tensile strength and the impact tensile resistance of the PLB films while slightly decreased its thermal stability. In addition, the compatibilizers of TDI and PLA-g-MA in the system not only affected the crystallinity and cold crystallization process of the PLB films, but also increased the mechanical properties of them due to the improvement of the interracial interaction between PLA and PBAT revealed by the morphological measurement. The synergistic effects of the nucleating agent and the compatibilizer afforded the blend films with increased tensile strength and impact tensile toughness, improved cold crystallization property and Xc.展开更多
The toughened poly(L-lactic acid)/poly(butylene succinate-butylene terephthalate)(PLLA/PBST) blend with enhanced melt strength and excellent low temperature toughness and strength was prepared by melt compounding thro...The toughened poly(L-lactic acid)/poly(butylene succinate-butylene terephthalate)(PLLA/PBST) blend with enhanced melt strength and excellent low temperature toughness and strength was prepared by melt compounding through in situ compatibilization reaction in presence of multifunctional epoxy compound(ADR).The PLLA/PBST blend was an immiscible system,and the compatibility of the PLLA/PBST blend was improved after adding ADR.FTIR and GPC curves confirmed the formation of the PLLA-g-PBST copolymer,which improved the interfacial bonding of the blend and therefore the PLLA/PBST/ADR blend showed excellent melt strength and mechanical properties.For the PLLA/PBST/ADR blend with 70/30 PLLA/PBST content,the complex viscosity increased significantly with increasing ADR content.Moreover,the tensile strength,elongation at break and impact strength all increased obviously with increasing the ADR content.The elongation at break of the blend reached the maximum value of 392.7%,which was 93.2 times that of neat PLLA.And the impact strength of the blend reached the maximum value of 74.7 k J/m~2,which was 21.3 times that of neat PLLA.Interestingly,the PLLA/PBST/ADR blend exhibited excellent lowtemperature toughness and strength.At –20 ℃,the elongation at break of the PLLA/PBST/ADR blend was as high as 93.2%,and the impact strength reached 18.8 k J/m~2.Meanwhile,the tensile strength of the blend at low temperature was also high(64.7 MPa),which was beneficial to the application of PLA in the low temperature field.In addition,the PLLA/PBST/ADR blend maintaind good biodegradability,which was of great significance to the wide application of PLLA.展开更多
A side-chain liquid crystalline ionomer（SLCI） was synthesized by grafting copolymerization of 4-（4-ethoxybenzoyloxy）-4＇-allyloxybiphenyl and N-allyl-pyridium bromide on polymethylhydrosiloxane. The SLCI was blend...A side-chain liquid crystalline ionomer（SLCI） was synthesized by grafting copolymerization of 4-（4-ethoxybenzoyloxy）-4＇-allyloxybiphenyl and N-allyl-pyridium bromide on polymethylhydrosiloxane. The SLCI was blended with polypropylene（PP） and polybutylene terephthalate（PBT） by melt mixing. The thermal behavior, liquid crystalline properties, morphological structure, and mechanical properties of the blends were investigated by differential scanning calorimetry（DSC）, polarizing optical microscopy（POM）, scanning electron microscopy（SEM）, and tensile measurement. When a proper amount of SLCI was added, fine configurations were formed in the PBT/PP/SLCI blend system, and the mechanical properties were improved due to improved adhesion at the interface. When excess SLCI was added, an inhomogeneous structure resulted, which caused the mechanical properties to deteriorate.展开更多
Methyl vinyl silicone rubber (MVQ)/polypropylene (PP) thermoplastic vulcanizate (TPV) combines the good melt processability, recyclability and sealing performance as well as biosafety, stain and fluid resistance, and ...Methyl vinyl silicone rubber (MVQ)/polypropylene (PP) thermoplastic vulcanizate (TPV) combines the good melt processability, recyclability and sealing performance as well as biosafety, stain and fluid resistance, and thus it is especially suitable in bio-safety areas and wearable electronic devices, etc. Nevertheless, the compatibility between MVQ and PP phases is poor. A big challenge on the compatibilization of MVQ/PP blends is that neither MVQ nor PP contains any reactive groups. In this study, a dual reactive compatibilizer composed of ethylenemethyl acrylate-glycidyl methacrylate terpolymer (EMA-co-GMA) and maleic anhydride grafted polypropylene (PP-g-MAH) was designed for the compatibilization of MVQ/PP blends. During melt blending, a copolymer compatibilizer at the MVQ/PP interface can be formed because of the in situ reaction between EMA-co-GMA and PP-g-MAH. The thermodynamic predict of its compatibilization effect through calculating the spreading coefficient of the in situ formed copolymer indicates that it can well compatibilize MVQ/PP blends. The experimental results show that under the GMA/MAH molar ratio of 0.5/1, the interface thickness largely increase from 102 nm for non-compatibilized blend to 406 nm, and the average size of MVQ dispersed phase largely decreases from 2.3 µm to 0.36 µm, the Tg of the two phases shifts toward each other, the mixing torque and mechanical properties of the blend are increased, all indicating its good compatibilization effect. This study provides a good compatibilizing method for immiscible MVQ/PP blends with no reactive groups in both components for the preparation of high performance MVQ/PP TPVs.展开更多
Fully biodegradable blends with low shape memory recovery temperature were obtained based on poly（lactic acid）（PLA） and poly（propylene carbonate）（PPC）. By virtue of their similar chemical structures, in situ c...Fully biodegradable blends with low shape memory recovery temperature were obtained based on poly（lactic acid）（PLA） and poly（propylene carbonate）（PPC）. By virtue of their similar chemical structures, in situ cross-linking reaction initiated by dicumyl peroxide（DCP） between PLA and PPC chains was realized in PLA/PPC blends. Therefore, the compatibility between PLA and PPC was increased, which obviously changed the phase structures and increased the elongation at break of the blends. The compatibilized blends had a recovery performance at 45 °C. Combining the changes of phase structures, the mechanism of the shape memory was discussed. It was demonstrated that in situ compatibilization by dicumyl peroxide was effective to obtain eco-friendly PLA/PPC blends with good mechanical and shape memory properties.展开更多
基金financially supported by the National Natural Science Foundation of China(No.52573053).
文摘Reactive compatibilization has been widely applied to enhance the compatibility of polymer blends,thereby improving their mechanical properties.However,it generally reduces the chain mobility and regularity,often leading to slower polymer crystallization.Here,we demonstrate that reactive compatibilization in poly(lactic acid)/poly(butylene adipate-co-terephthalate)(PLA/PBAT)blends unexpectedly promotes PLA matrix crystallization during injection molding,in contrast to the retarded kinetics observed in differential scanning calorimetry isothermal crystallization studies.The phase morphology,rheological behavior,and crystalline structure were systematically analyzed to elucidate markedly different crystallization kinetics under static and shear fields.The potential mechanism underlying crystallization enhancement is attributed to PBAT domain refinement and viscosity increase induced by reactive compatibilization,which,under shear flow,create favorable conditions for crystallization by enhancing PBAT fibril nucleation and retarding the relaxation of oriented PLA chains.This study offers new perspectives on the effect of reactive compatibilization on the polymer crystallization behavior.
文摘In-situ reactive compatibilization of high-density polyethylene （HDPE）/ground tire rubber （GTR） blends by dicumyl peroxide （DCP） and HY-2045 - a kind of thermoplastic phenolic resin without catalyst was investigated by studying the mor-phology, stress and strain behavior, dynamic mechanical properties and crystallization performance of the blends. Scanning e-lectron microscopy （SEM） results show that there are a lot of fibrous materials distributing in the interface, which connects the dispersed phase with the matrix and obtains better interfacial strength for prominent mechanical properties. The addition of compatibilizers results in the decrease of crystallinity of the blends and the disappearance of an obvious yield phenomenon, which was proved by the differential scanning calorimeter （DSC） test and X-ray diffraction （XRD） characterization Although the crystallinity of the blends decreases,the tensile strength and tensile strain of the blends significantly increases, especially for the HDPE/GTR/DCP/HY-2045 blends, which is possibly attributed to the good compatibility of the blends owing to the in-situ interface crosslinking. In addition, it is found that the compatibilizing HDPE/GTR blends shows a higher tan^ peak temperature and a broaden transition peak for GTR phase.
基金financially supported by the National Natural Science Foundation of China(No.21004069)
文摘The influences of hyperbranched polyethylenimine （hPEI）, which possesses many reactive amino end-groups, on the blending properties of bisphenol-A polycarbonate （PC） and amorphous polyamide （aPA） were systematically investigated. Scanning electron microscopy （SEM） and differential scanning calorimetry （DSC） were used to observe the effect of hPE1 on morphologies of PC and aPA phases in bulk blends. While the interfacial fracture toughness between planar PC and aPA layers with and without hPEI was studied by using augmented double cantilever beam （ADCB） method. Results show that the compatibility in PC/aPA blends can be significantly improved by adding a small amount of hPEI, mainly due to the interchange reactions between the polymers leading to the formation of block copolymers, cross-linked polymers and molecules with other constitutions. The augmented double cantilever beam experiments showed that the reactive process drastically reinforced the interfacial adhesion between planar layers of PC and aPA. However, degradation takes place during annealing at 180℃, which was responsible for the production of small molar mass species of PC.
文摘Melt blending of biodegradable polyesters such as poly(lactic acid)(PLA)and poly(butylene adipate co-terephthalate)(PBAT)with a compatibilizer and natural filler offers a chance to develop biodegradable biocomposites with improved performance.In this study,we examined how PLA/PBAT blends behave during ultimate biodegradation(mineralization),both with and without compatibilizer and algae as a reinforcement,under controlled composting conditions using carbon dioxide(CO_(2))respirometry techniques.Throughout the biodegradation process,the disintegration behaviour,thermal,chemical,and morphological properties of test samples before and after biodegradation were analyzed using FTIR,TGA,DSC,and SEM techniques.The results from CO_(2)biodegradation showed that PLA/PBAT blend exhibits a higher rate of biodegradation compared to neat PLA and PBAT.The addition of algae to a compatibilized PLA/PBAT blend showed an enhanced biodegradation rate due to hydrolytic cleavage and microbial assimilation.This was further supported by the disintegration test,where algae-reinforced composites showed fragmentation within 30 days.FTIR,TGA and SEM analysis revealed the structural changes that occurred during biodegradation,highlighting the role of algae in affecting the thermal stability and surface morphology.After the compost biodegradation step,eco-toxicity seed germination was conducted on the test samples.Plant seed germination test results confirmed that all test samples achieved maximumgermination.This indicates there were no toxic residues,suggesting that the degraded materials are environmentally safe.Overall,this study contributes to the understanding of biodegradation mechanisms and the ecological impact of bio-based polymer composites as eco-friendly materials and products.
基金financially supported by Development and Promotion of Science and Technology Talents (DPST) (No. 013/2559)
文摘Polylactide(PLA)films blended with poly(butylene adipate-co-terephthalate)(PBAT)were hot melted using a twin screw extruder with the addition of triethyl citrate(TEC)as a plasticizer and toluene diisocyanate(TDI)as a compatibilizer.The synergistic effects of the two additives on the mechanical,thermal,and morphological properties of the PLA/PBAT blend films were investigated.The influence of TEC content on the plasticized PLA films and the effect of TDI’s presence on the PLA/PBAT blend films were also studied by comparing them with neat PLA.The results showed a pronounced increase in elongation at break of the plasticized PLA films with increasing TEC levels,but a slight reduction in thermal stability.Also,the addition of TEC and TDI to the blend system not only synergistically enhanced the tensile properties and tensile-impact strength of the PLA/PBAT blends,but also affected their crystallinity and cold crystallization rate,a result of the improvement of interfacial interaction between PLA and PBAT,including the enhancement of their chain mobility.The synergy of the plasticization and compatibilization processes led to the improvement of tensile properties,tensile-impact strength,and compatibility of the blends,accelerating cold crystallization without affecting crystallization.
基金financially supported by the Prince of Songkla University(No.SCI570376S)the Development and Promotion of Science and Technology Talents project(DPST)
文摘Polylactide （PLA） films blended with 10 wt% poly（butylene adipate-co-terephthalate） （PBAT） were prepared by using a twin screw extruder in the presence of the nucleating agent of titanium dioxide （TiO2） and the compatibilizers of toluene diisocyanate （TDI） and PLA-grafted-maleic anhydride （PLA-g-MA）. The synergistic effect of the nucleation and compatibilization on the properties and crystallization behavior of the PLA/PBAT （PLB） films was explored. The results showed that the addition of TiO2 significantly enhanced the tensile strength and the impact tensile resistance of the PLB films while slightly decreased its thermal stability. In addition, the compatibilizers of TDI and PLA-g-MA in the system not only affected the crystallinity and cold crystallization process of the PLB films, but also increased the mechanical properties of them due to the improvement of the interracial interaction between PLA and PBAT revealed by the morphological measurement. The synergistic effects of the nucleating agent and the compatibilizer afforded the blend films with increased tensile strength and impact tensile toughness, improved cold crystallization property and Xc.
基金financially supported by the Science and Technology Development Plan of Jilin Province (No. 20210203199SF)。
文摘The toughened poly(L-lactic acid)/poly(butylene succinate-butylene terephthalate)(PLLA/PBST) blend with enhanced melt strength and excellent low temperature toughness and strength was prepared by melt compounding through in situ compatibilization reaction in presence of multifunctional epoxy compound(ADR).The PLLA/PBST blend was an immiscible system,and the compatibility of the PLLA/PBST blend was improved after adding ADR.FTIR and GPC curves confirmed the formation of the PLLA-g-PBST copolymer,which improved the interfacial bonding of the blend and therefore the PLLA/PBST/ADR blend showed excellent melt strength and mechanical properties.For the PLLA/PBST/ADR blend with 70/30 PLLA/PBST content,the complex viscosity increased significantly with increasing ADR content.Moreover,the tensile strength,elongation at break and impact strength all increased obviously with increasing the ADR content.The elongation at break of the blend reached the maximum value of 392.7%,which was 93.2 times that of neat PLLA.And the impact strength of the blend reached the maximum value of 74.7 k J/m~2,which was 21.3 times that of neat PLLA.Interestingly,the PLLA/PBST/ADR blend exhibited excellent lowtemperature toughness and strength.At –20 ℃,the elongation at break of the PLLA/PBST/ADR blend was as high as 93.2%,and the impact strength reached 18.8 k J/m~2.Meanwhile,the tensile strength of the blend at low temperature was also high(64.7 MPa),which was beneficial to the application of PLA in the low temperature field.In addition,the PLLA/PBST/ADR blend maintaind good biodegradability,which was of great significance to the wide application of PLLA.
基金Supported by the National Natural Science Foundation of China(No50673105)
文摘A side-chain liquid crystalline ionomer（SLCI） was synthesized by grafting copolymerization of 4-（4-ethoxybenzoyloxy）-4＇-allyloxybiphenyl and N-allyl-pyridium bromide on polymethylhydrosiloxane. The SLCI was blended with polypropylene（PP） and polybutylene terephthalate（PBT） by melt mixing. The thermal behavior, liquid crystalline properties, morphological structure, and mechanical properties of the blends were investigated by differential scanning calorimetry（DSC）, polarizing optical microscopy（POM）, scanning electron microscopy（SEM）, and tensile measurement. When a proper amount of SLCI was added, fine configurations were formed in the PBT/PP/SLCI blend system, and the mechanical properties were improved due to improved adhesion at the interface. When excess SLCI was added, an inhomogeneous structure resulted, which caused the mechanical properties to deteriorate.
基金supported by the National Natural Science Foundation of China(No.51525301).
文摘Methyl vinyl silicone rubber (MVQ)/polypropylene (PP) thermoplastic vulcanizate (TPV) combines the good melt processability, recyclability and sealing performance as well as biosafety, stain and fluid resistance, and thus it is especially suitable in bio-safety areas and wearable electronic devices, etc. Nevertheless, the compatibility between MVQ and PP phases is poor. A big challenge on the compatibilization of MVQ/PP blends is that neither MVQ nor PP contains any reactive groups. In this study, a dual reactive compatibilizer composed of ethylenemethyl acrylate-glycidyl methacrylate terpolymer (EMA-co-GMA) and maleic anhydride grafted polypropylene (PP-g-MAH) was designed for the compatibilization of MVQ/PP blends. During melt blending, a copolymer compatibilizer at the MVQ/PP interface can be formed because of the in situ reaction between EMA-co-GMA and PP-g-MAH. The thermodynamic predict of its compatibilization effect through calculating the spreading coefficient of the in situ formed copolymer indicates that it can well compatibilize MVQ/PP blends. The experimental results show that under the GMA/MAH molar ratio of 0.5/1, the interface thickness largely increase from 102 nm for non-compatibilized blend to 406 nm, and the average size of MVQ dispersed phase largely decreases from 2.3 µm to 0.36 µm, the Tg of the two phases shifts toward each other, the mixing torque and mechanical properties of the blend are increased, all indicating its good compatibilization effect. This study provides a good compatibilizing method for immiscible MVQ/PP blends with no reactive groups in both components for the preparation of high performance MVQ/PP TPVs.
基金financially supported by the National Natural Science Foundation of China(No.51503117)the Innovation Foundation for Graduate Students of Shandong University of Science and Technology,China(No.SDKDYC170334)
文摘Fully biodegradable blends with low shape memory recovery temperature were obtained based on poly（lactic acid）（PLA） and poly（propylene carbonate）（PPC）. By virtue of their similar chemical structures, in situ cross-linking reaction initiated by dicumyl peroxide（DCP） between PLA and PPC chains was realized in PLA/PPC blends. Therefore, the compatibility between PLA and PPC was increased, which obviously changed the phase structures and increased the elongation at break of the blends. The compatibilized blends had a recovery performance at 45 °C. Combining the changes of phase structures, the mechanism of the shape memory was discussed. It was demonstrated that in situ compatibilization by dicumyl peroxide was effective to obtain eco-friendly PLA/PPC blends with good mechanical and shape memory properties.
