A polylactide(PLA)blend with simultaneous enhancement of strength,toughness,and heat resistance was successfully achieved by adding biodegradable poly(propylene carbonate)(PPC)and uniaxial pre-stretching.The effects o...A polylactide(PLA)blend with simultaneous enhancement of strength,toughness,and heat resistance was successfully achieved by adding biodegradable poly(propylene carbonate)(PPC)and uniaxial pre-stretching.The effects of the PPC content(0 wt%-50 wt%)on the phase morphology and performance of the blends before and after pre-stretching were systematically investigated.Blending PPC initially reduced the strength,modulus,and heat resistance,but pre-stretching significantly enhanced these properties.In blends containing≤30 wt%PPC,where PPC formed a well-dispersed island-like phase within the PLA matrix,pre-stretching simultaneously enhanced strength,toughness,and heat resistance.The optimized pre-stretched 70/30 PLA/PPC(ps-70/30)blend achieved exceptional performance:tensile strength increased from 66.9MPa to 84.5 MPa,elongation at break dramatically improved from 6.8%to 115.1%,impact strength reached 55.1 k J/m^(2)(far exceeding neat PLA's 3.5 k J/m^(2)),and Vicat softening temperature(VST)increased by 60.6%to 101.8℃.Notably,the ps-70/30 blend retained excellent mechanical properties even after six months of aging.These improvements were attributed to the synergistic effects of the PPC incorporation and prestretching.PPC not only promoted the high orientation of the PLA molecular chains but also facilitated the formation of a stable crystalline phase during pre-stretching,thereby enhancing both the mechanical properties and heat resistance.However,when the PPC content exceeded 30wt%,phase inversion occurred,resulting in a continuous amorphous PPC phase that degraded the overall performance.This study demonstrated that a combination of controlled PPC incorporation and pre-stretching can effectively overcome PLA's brittleness of PLA while improving its heat resistance,offering a promising strategy for developing high-performance,fully biodegradable PLA materials suitable for industrial applications.展开更多
A new principle for producing fire-resistant polymer materials with increased deformation properties using a flame retardant not as a heterogeneous additive,but as a thermoplastic flame retardant in a hybrid polymer m...A new principle for producing fire-resistant polymer materials with increased deformation properties using a flame retardant not as a heterogeneous additive,but as a thermoplastic flame retardant in a hybrid polymer mixture with a polyhydrocarbon is considered.Hybrid polymer blends of low-molecular ammonium polyphosphate(APP)with an ethylene-vinyl acetate copolymer(EVA)with an APP content of 80 wt%with enhanced deformation properties were obtained by extrusion mixing at various temperatures in the range from 200°C to 250°C.A chemical scheme for the transformations of the components during the formation of the composite is proposed.X-ray diffraction analysis showed the formation of new crystalline structures of APP.The phase structure of the systems corresponding to the model of a dispersed-filled composite in which EVA plays the role of a matrix,determining the deformation of the mixture,and the filler is ammonium polyphosphate,was studied by scanning electron microscopy(SEM).The method of FTIR microscopy showed chemical interactions between EVA and APP with the formation of amide groups.The conditions for obtaining compositions characterized by heat resistance of 210°C,oxygen index of 55 and ultimate elongation at drawing of 213%were established.展开更多
We investigated the phase behavior of diblock copolymer AB/homopolymer C blends in concentrated aqueous solutions using a simulated annealing method.Phase diagrams were constructed as a function of the concentration o...We investigated the phase behavior of diblock copolymer AB/homopolymer C blends in concentrated aqueous solutions using a simulated annealing method.Phase diagrams were constructed as a function of the concentration of all polymers(Φ)and the volume fraction of homopolymer(fC).Rich phase transition sequences were observed,especially reentrant phase transitions,such as lamellae→inverted cylinders→gyroids→lamellae→disorder,for a givenΦwith increasing fC.By analyzing the variations in the average contact numbers between different components and the effective volume fractions of B-domains,we elucidated the mechanisms of the reentrant phase transitions.We found that the strong attraction between B and C leads to the swelling of B-domains upon addition of homopolymer.Concurrently,the solvent preferentially swells the A-domains over the B+C-domains.The competing swelling effects of the solvent and homopolymer on the A-domains and B-domains,respectively,triggered the reentrant phase behavior in the symmetric AB copolymer system upon addition of homopolymer.展开更多
The equilibrium dynamics and nonlinear rheology of unentangled polymer blends remain inadequately understood,especially regarding the influence of short-chain matrix length N_(S) on the structure and rheological behav...The equilibrium dynamics and nonlinear rheology of unentangled polymer blends remain inadequately understood,especially regarding the influence of short-chain matrix length N_(S) on the structure and rheological behavior of dispersed long chains.Using molecular dynamics simulations based on the Kremer-Grest model,we systematically explore the N_(S)-dependence of static conformations,equilibrium dynamics,and nonlinear shear responses in unentangled long-chain/short-chain polymer blends.Our results demonstrate a decoupling between the static and dynamic sensitivity to N_(S):while the static chain size,R_g,follows Flory theory with slight swelling at small N_(S) due to incomplete excluded volume screening,the diffusion coefficient,D,and the relaxation time,τ_(0),exhibit a strong,non-monotonic N_(S)-dependence,transitioning from monomeric friction dominance at small N_(S) to collective segmental rearrangement at large N_(S).Additionally,we observe partial decoupling between the viscous and normal stress responses:while the zero-shear viscosity,η,is strongly N_(S)-dependent,the first and second normal stress coefficients,Ψ_(1) and Ψ_(2),collapse onto universal curves when scaled by the dimensionless shear rate,γτ_(0),suggesting a common mechanism of orientation and stretching.Under shear,long chains compress in the vorticity direction λ_(z)~Wi^(-0.2),which reduces collision frequency and contributes to shear thinning,while the scaling of weaker orientation resistance m_(G)~Wi^(0.35)reflects hydrodynamic screening by the short-chain matrix.These findings highlight the limitations of single-chain models and emphasize the necessity of considering N_(S)-dependent matrix dynamics and flow-induced structural changes in understanding the rheology of unentangled polymer blends.展开更多
Hybrid organic-inorganic perovskites have been the subject of recent intense interest due to advances in photovoltaic and other optoelectronic applications. However, their poor stability limits commercial market appli...Hybrid organic-inorganic perovskites have been the subject of recent intense interest due to advances in photovoltaic and other optoelectronic applications. However, their poor stability limits commercial market application We enhance water stability by post treatment preparation of hybrid metal halide perovskite nanocrystal-embedded polymethylmethacrylate （PM- MA） blend films. Through blending process without any cleaning of nanocrystals, crystalline hybrid organic-inorganic perovs-kite nanocrystals were incorporated into PMMA matrix with well-dispersion Passivation of PMMA on the surface of the per-ovskite nanocrystals results in decreased traps and a long photoluminescence （PL） lifetime despite the bromine vacancies in the crystal lattice. Moreover, such color purity and inherent high transmittance for fluorescence emission of perovskite nanocrystals will endow the films with promising potentials in diverse practice photonic applications.展开更多
The effect of maleic anhydride grafted styrene-ethylene- buty-lene-styrene block copolymer （SEBS-g-MAH） and in-situ grafting MAH on mechanical, dynamic mechanical properties of wood flour/recycled plastic blends com...The effect of maleic anhydride grafted styrene-ethylene- buty-lene-styrene block copolymer （SEBS-g-MAH） and in-situ grafting MAH on mechanical, dynamic mechanical properties of wood flour/recycled plastic blends composites was investigated. Recycled plastic polypro-pylene （PP）, high-density polyethylene （HDPE） and polystyrene （PS）, were mixed with wood flour in a high speed blender and then extruded by a twin/single screw tandem extruder system to form wood flour/recycled plastic blends composites. Results show that the impact properties of the composites were improved more significantly by using SEBS-g-MAH compatibilizer than by using the mixtures of MAH and DCP via reactive blending in situ. However, contrary results were ob-served on the tensile and flexural properties of the corresponding com-posites. In General, the mechanical properties of composites made from recycled plastic blends were inferior to those made from virgin plastic blends, especially in elongation break. The morphological study verified that the interfacial adhesion or the compatibility of plastic blends with wood flour was improved by adding SEBS-g-MAH or in-situ grafting MAH. A better interfacial bonding between PP, HDPE, PS and wood flour was obtained by in-situ grafting MAH than the addition of SEBS-g-MAH. In-situ grafting MAH can be considered as a potential way of increasing the interfacial compatibility between plastic blends and wood flour. The storage modulus and damping factor of composites were also characterized through dynamic mechanical analysis （DMA）.展开更多
Fuel injection properties,including the injection rate(temporal aspects)and spray behavior(spatial aspects),play a crucial role in the combustion efficiency and emissions of diesel engines.This study investigates the ...Fuel injection properties,including the injection rate(temporal aspects)and spray behavior(spatial aspects),play a crucial role in the combustion efficiency and emissions of diesel engines.This study investigates the effects of different ethanol-biodiesel-diesel(EBD)blends on the injection performance in diesel engines.Experimental tests are conducted to examine key injection parameters,such as spray penetration distance,spray cone angle,and droplet size,alongside an analysis of coupling leakage.The main findings are as follows:(1)The injection behavior of ethanol and diesel differs significantly.The addition of ethanol reduces the density,viscosity,and modulus of elasticity of the fuel mixture.While the injection advance angle,penetration distance,and Sauter mean diameter show minimal changes,the spray cone angle and coupling leakage increase notably.These alterations may disrupt the“fuelair-chamber”matching characteristics of the original engine,potentially affecting performance.(2)In contrast,the injection performance of biodiesel ismore similar to that of diesel.As biodiesel content increases,the density,viscosity,and modulus of elasticity of the blended fuel also grow.Though changes in injection timing,penetration distance,and spray cone angle remain minimal,the Sauter mean diameter experiences a slight increase.The“air-fuel chamber”compatibility of the original engine is largely unaffected,though fuel atomization slightly deteriorates.Blending up to 20%biodiesel and 30%ethanol with diesel effectively compensates for the shortcomings of using single fuels,maintaining favorable injection dynamics while enhancing lubrication and sealing performance of engine components.展开更多
Aim To investigate the melting behavior of polyamide 6 in polyamide 6/polyethy lene blends crystallized from amorphous state. Methods DSC was used to test effects of annealing temperature, annealing time, DS...Aim To investigate the melting behavior of polyamide 6 in polyamide 6/polyethy lene blends crystallized from amorphous state. Methods DSC was used to test effects of annealing temperature, annealing time, DSC scan rate, and the step wise annealing on the melting peaks of the ice water quenched specimens. Results and Conclusion Varied melting peaks of PA6 component were obtained. The degree of perfection and the crystallization degree of PA6 crystals decreased in the blends, and the crystallization degree of PA6 increased with the increasing of the annealing time. The height of the upper melting peak of reference PA6 is higher than that in blends.展开更多
Aim To investigate the multiple melting behavior of polyamide 6(PA 6) in polyamide 6/linear low density polyethylene blends crystallized from the crystal amorphous state. Methods\ The effects of annealing tempera...Aim To investigate the multiple melting behavior of polyamide 6(PA 6) in polyamide 6/linear low density polyethylene blends crystallized from the crystal amorphous state. Methods\ The effects of annealing temperature, annealing time, heating rate, and the step wise annealing were measured by DSC. Results and Conclusion\ There exists a critical heating rate affecting the middle temperature melting peak. When annealed at the temperature close to the melting peak, the main melting peak of PA 6 shifted to a higher temperature. Within a short time, annealing time has much effect on neat PA 6 but little effect on PA 6 in the blends. Addition of PE results in a decreasing in the height of melting peak. These phenomenon show that the melting behavior of PA 6 was affected by PE, compatibilizer, as well as thermal treatment.展开更多
The thermal behavior of thermotropic hydroxyethyl cellulose acetate (HECA)/polyethylene (PE) blends has been studied by DSC. It is found that the blends of HECA and PE are immiscible but the crystallization of PE is a...The thermal behavior of thermotropic hydroxyethyl cellulose acetate (HECA)/polyethylene (PE) blends has been studied by DSC. It is found that the blends of HECA and PE are immiscible but the crystallization of PE is affected by HECA chains in the blends with more than 50% HECA, which results in the subordinate crystallization of PE and the formation of imperfect structures in the PE crystals. The imperfection of PE crystals in the blends can be eliminated after annealing at 393K.展开更多
Series of PVC/ABS and PVC/SBS blends of composition 20/ 80. 40/ 60, 60 / 40 and 80 / 20were prepared in a screw extruder. The phase morphology, miscibility and rheological behaviour of two systems were investigated. T...Series of PVC/ABS and PVC/SBS blends of composition 20/ 80. 40/ 60, 60 / 40 and 80 / 20were prepared in a screw extruder. The phase morphology, miscibility and rheological behaviour of two systems were investigated. The viscosity-composition plots were represented by sub-cluster equation, the various differences between two systems are interpreted with the equation parameters展开更多
Shape memory polymer （SMP） blends based on polyurethane （PU） and polyaniline （PANI） were prepared via chemical in situ polymerization process. The thermal, mechanical, electrical and shape memory properties were...Shape memory polymer （SMP） blends based on polyurethane （PU） and polyaniline （PANI） were prepared via chemical in situ polymerization process. The thermal, mechanical, electrical and shape memory properties were investigated. The structural characterization and morphology of the polymer blends were inspected by Fourier transform infrared （FTIR） and scanning electron microscopy （SEM）, respectively. The 1 wt% of PANI loading enhanced the thermal stability of the system up to 339 ~C. According to differential scanning calorimetry （DSC）, the glass transition temperature （Tg） and melting temperature （Tm） of PU/PANI blends increased with the polyaniline loading （0.1 wt%-l wt%）. Improved mechanical properties such as tensile strength and Young＇s modulus of PU matrix were also observed with PANI. Moreover, the electrical conductivity of PU/PANI blends was also found to be a function of PANI loading. Remarkable recoverability of thermally triggered shape memory （SM） behavior to the extent of 96% was achieved for 1 wt% PANI blend.展开更多
The molecular weight of a polymer is of prime importance and greatly influences the processing and mechanical properties of the polymer.Trans-1,4-poly(butadiene-co-isoprene)multi-block copolymer rubbers(TBIR)exhibit o...The molecular weight of a polymer is of prime importance and greatly influences the processing and mechanical properties of the polymer.Trans-1,4-poly(butadiene-co-isoprene)multi-block copolymer rubbers(TBIR)exhibit outstanding fatigue resistance,low heat build-up and good abrasion resistance,and are expected to be desirable candidate for high performance tire.Study on the influence of TBIR with different molecular weights on the structure and properties of TBIR and natural rubber(NR)/TBIR blends is essential to understand its contribution to the greatly improved dynamic properties of the rubber vulcanizates.TBIR with different molecular weights characterized by 1H-NMR,13C-NMR,GPC,and DSC were highly trans-1,4-copolymers with similar chain sequence distribution and crystalline trans-1,4-polyisoprene(TPI)blocks.The green strength and modulus of TBIR increased with the increasing molecular weight.The NR/TBIR compounds filled with 40 phr carbon black were chemically cured by sulfur for the preparation of NR/TBIR vulcanizates.The compatibility between NR and TBIR,filler distribution,crosslinking bond and density,and properties of NR/TBIR vulcanizates were studied.The NR/TBIR vulcanizates showed increasing tensile strength,hardness,modulus,rebound,abrasion resistance,and flexural fatigue properties with increasing molecular weight of TBIR.Furthermore,they presented significant improvement in flexural fatigue resistance when compared with that of NR vulcanizate.The contribution mechanism of TBIR on the NR/TBIR blends was discussed.The TBIR with a wide range of molecular weight are ideal rubbers for high performance tires.展开更多
Sustainable blends of poly(propylene carbonate)(PPC)and stereocomplex polylactide(sc-PLA)were prepared by melt blending equimolar poly(L-lactic acid)(PLLA)and poly(D-lactide acid)(PDLA)with PPC to form sc-PLA crystals...Sustainable blends of poly(propylene carbonate)(PPC)and stereocomplex polylactide(sc-PLA)were prepared by melt blending equimolar poly(L-lactic acid)(PLLA)and poly(D-lactide acid)(PDLA)with PPC to form sc-PLA crystals in situ in the melt blending process.Differential seanning calorimetry analysis revealed that only sc-PLA,no homo-crystallization of PLLA or PDLA,formed in the PPC matrix as the sc-PLA con tent was more than 10 wt%.Very in triguingly,scan ning electronic microscopy observati on showed that sc-PLA was evenly dispersed in the PPC phase as spherical particles and the sizes of sc-PLA particles did not obviously increase with in creasing sc-PLA con tent.As a con seque nee,the rheological properties of PPC were greatly improved by incorporation of sc-PLA.When the sc-PLA con tent was 20 wt%,a percolati on n etwork structure was formed,and the blends showed solid-like behavior.The sc-PLA particles could reinforce the PPC matrix,especially at a temperature above the glass transition temperature of PPC.Moreover,the Vicat softening temperature of PPC/sc-PLA blends could be increased compared with that of neat PPC.展开更多
Poly（propylene carbonate） （PPC） was melt blended in a batch mixer with poly（butylene carbonate） （PBC） in an effort to improve the toughness of the PPC without compromising its biodegradability and biocompatibi...Poly（propylene carbonate） （PPC） was melt blended in a batch mixer with poly（butylene carbonate） （PBC） in an effort to improve the toughness of the PPC without compromising its biodegradability and biocompatibility. DMA results showed that the PPC/PBC blends were an immiscible two-phase system. With the increase in PBC content, the PPC/PBC blends showed decreased tensile strength, however, the elongation at break was increased to 230% for the 50/50 PPC/PBC blend. From the tensile strength experiments, the Pukanszky model gave credit to the modest interfacial adhesion between PPC and PBC, although PPC/PBC was immscible. The impact strength increased significantly which indicated the toughening effects of the PBC on PPC. SEM examination showed that cavitation and shear yielding were the major toughening mechanisms in the blends subjected the impact tests. TGA measurements showed that the thermal stability of PPC decreased with the incorporation of PBC. Rheological investigation demonstrated that the addition of PBC reduced the value of storage modulus, loss modulus and complex viscosity of the PPC/PBC blends to some extent. Moreover, the addition of PBC was found to increase the processability of PPC in extrusion. The introduction of PBC provided an efficient and novel toughened method to extend the application area of PPC.展开更多
A simultaneous increase of both stiffness and extensibility ofpoly（ethylene glycol-co-cyclohexane-1,4-dimethanol terephthalate） （PETG）/polycarbonate （PC） blends prepared through the slit die extrusion-uniaxial c...A simultaneous increase of both stiffness and extensibility ofpoly（ethylene glycol-co-cyclohexane-1,4-dimethanol terephthalate） （PETG）/polycarbonate （PC） blends prepared through the slit die extrusion-uniaxial cold stretching process was observed. The stretched sheets have a unique mechanical character that an increased tensile modulus is accompanied by an increased extensibility with increasing the draw ratio. Especially, a sharp increasing of the extensibility is observed for PETG/PC （70/30 wt%） blends at draw ratios between 8.2 and 20.0, where a nine times increase of extensibility is achieved. The mechanism of stretching-induced superior extensibility is investigated via micrograph observation, rheometry and calorimetric analysis. The observed superior extensibility could be tentatively explained by the bridging effect of the PC microfibrils on the crack development during tensile failure.展开更多
Metallocene-catalyzed linear low-density polyethylene/polypropylene （mLLDPE/PP） blends were prepared by ultrasonic extrusion in this work. Their extrusion processing behaviors were estimated by online measured data,...Metallocene-catalyzed linear low-density polyethylene/polypropylene （mLLDPE/PP） blends were prepared by ultrasonic extrusion in this work. Their extrusion processing behaviors were estimated by online measured data, such as the die pressure and flow rate. Crystallization and mechanical properties of the blends were also investigated. The results show that the addition of PP improves the processing behaviors of mLLDPE, but has little effect on its mechanical properties. On the other hand, the addition of mLLDPE improves the impact strength of PP, but has little effect on its processing behavior. The processing behaviors and mechanical properties of mLLDPE/PP blends get further improved due to the presence of ultrasonic oscillation during extrusion. Compared with PP-rich blends, the apparent viscosity drop of mLLDPE-rich blends is more sensitive to ultrasonic oscillation. The ultrasonic oscillation affects the crystal nucleation, while barely the other crystalline behaviors of the blends.展开更多
Phase separation was studied by the optical microscopy in blends of nylon 6 (PA6) with sodium salt of ethylene/methacrylic acid copolymer (PEMA).The image collecting technology was used to keep track of the developme...Phase separation was studied by the optical microscopy in blends of nylon 6 (PA6) with sodium salt of ethylene/methacrylic acid copolymer (PEMA).The image collecting technology was used to keep track of the development of blends at a certain temperature.The fractal dimension of phase separation was calculated by the image solving technology according to the fractal theory and the self similarity behavior of the process was proved.The relationship of the fractal behavior with composition and experimental temperature was discussed.The fractal behavior of the crystallization development of the crystal phase of PA6 in blends was also discussed and the fractal behavior calculated.展开更多
The effect of PBS on the morphological features of PVDF has been investigated by optical and atomic force microscopies under various conditions. It was found that neat PVDF forms large γform spherulites with extraord...The effect of PBS on the morphological features of PVDF has been investigated by optical and atomic force microscopies under various conditions. It was found that neat PVDF forms large γform spherulites with extraordinarily weak birefringence at 170℃. Adding 30% PBS makes PVDF exhibit intrigued flower-like spherulitic morphology. The growth mechanism was explained by the decrease of the supercooling and the materials dissipation. Increasing the PBS content to 70% favors the formation of ring banded spherulites. Temperature dependent experiments verify the α→γ phase transition occurs from the junction sites of the ot and y crystals, while starts from the centers of α spherulites in the blends. Ring banded structures could be observed in neat PVDF, 70/30 blend and 30/70 blend when crystallized at 155℃, without γ crystals. The band period of PVDF α spherulites increases with crystallization temperature as well as the amount of PBS content. At 140℃, spherulites in neat PVDF lose their ring banded feature, while coarse spherulites consisting of evident lamellar bundles could be found in 30/70 blend.展开更多
In this work, polypropylene (PP)/polystyrene (PS) blends with different organoclay concentrations were prepared via melt compounding. Differing from the results of previous reports, the organoclay platelets are mostly...In this work, polypropylene (PP)/polystyrene (PS) blends with different organoclay concentrations were prepared via melt compounding. Differing from the results of previous reports, the organoclay platelets are mostly located in the dispersed PS phase instead of the interface. The dimensions of the dispersed PS droplets are greatly reduced and apparent compatibilization effect still exists, which cannot be explained by the traditional compatibilization mechanism. A novel compatibilization mecha- nism, "cutting" to apparently compatibilize the immiscible PP/PS blends was proposed. The organoclay platelets tend to form a special "knife-like structure" in the PS domain under the shear stress of the continuous PP phase during compounding. The "clay knife" can split the dispersed PS domain apart and lead to the dramatic reduction of the dispersed domain size.展开更多
基金supported by the Science and Technology Development Plan of Jilin Province(No.YDZJ202403009CGZH)Engineering Research Center of Coalbased Ecological Carbon Sequestration Technology of the Ministry of Education(No.MJST2025-1)+2 种基金Chinese Academy of Sciences(Changchun Branch)(No.2024SYHZ0038)Development and Reform Commission of Jilin Province of China(No.2024C019-5)Science and Technology Bureau of Changchun City of China(No.23SH08)。
文摘A polylactide(PLA)blend with simultaneous enhancement of strength,toughness,and heat resistance was successfully achieved by adding biodegradable poly(propylene carbonate)(PPC)and uniaxial pre-stretching.The effects of the PPC content(0 wt%-50 wt%)on the phase morphology and performance of the blends before and after pre-stretching were systematically investigated.Blending PPC initially reduced the strength,modulus,and heat resistance,but pre-stretching significantly enhanced these properties.In blends containing≤30 wt%PPC,where PPC formed a well-dispersed island-like phase within the PLA matrix,pre-stretching simultaneously enhanced strength,toughness,and heat resistance.The optimized pre-stretched 70/30 PLA/PPC(ps-70/30)blend achieved exceptional performance:tensile strength increased from 66.9MPa to 84.5 MPa,elongation at break dramatically improved from 6.8%to 115.1%,impact strength reached 55.1 k J/m^(2)(far exceeding neat PLA's 3.5 k J/m^(2)),and Vicat softening temperature(VST)increased by 60.6%to 101.8℃.Notably,the ps-70/30 blend retained excellent mechanical properties even after six months of aging.These improvements were attributed to the synergistic effects of the PPC incorporation and prestretching.PPC not only promoted the high orientation of the PLA molecular chains but also facilitated the formation of a stable crystalline phase during pre-stretching,thereby enhancing both the mechanical properties and heat resistance.However,when the PPC content exceeded 30wt%,phase inversion occurred,resulting in a continuous amorphous PPC phase that degraded the overall performance.This study demonstrated that a combination of controlled PPC incorporation and pre-stretching can effectively overcome PLA's brittleness of PLA while improving its heat resistance,offering a promising strategy for developing high-performance,fully biodegradable PLA materials suitable for industrial applications.
基金financially supported by Ministry of Science and Higher Education of the Russian Federation.
文摘A new principle for producing fire-resistant polymer materials with increased deformation properties using a flame retardant not as a heterogeneous additive,but as a thermoplastic flame retardant in a hybrid polymer mixture with a polyhydrocarbon is considered.Hybrid polymer blends of low-molecular ammonium polyphosphate(APP)with an ethylene-vinyl acetate copolymer(EVA)with an APP content of 80 wt%with enhanced deformation properties were obtained by extrusion mixing at various temperatures in the range from 200°C to 250°C.A chemical scheme for the transformations of the components during the formation of the composite is proposed.X-ray diffraction analysis showed the formation of new crystalline structures of APP.The phase structure of the systems corresponding to the model of a dispersed-filled composite in which EVA plays the role of a matrix,determining the deformation of the mixture,and the filler is ammonium polyphosphate,was studied by scanning electron microscopy(SEM).The method of FTIR microscopy showed chemical interactions between EVA and APP with the formation of amide groups.The conditions for obtaining compositions characterized by heat resistance of 210°C,oxygen index of 55 and ultimate elongation at drawing of 213%were established.
基金financially supported by the Natural Science Foundation of Shandong Province(Nos.ZR2023QA136,ZR2021MA073 and ZR2024QA235)the National Natural Science Foundation of China(No.22173051).
文摘We investigated the phase behavior of diblock copolymer AB/homopolymer C blends in concentrated aqueous solutions using a simulated annealing method.Phase diagrams were constructed as a function of the concentration of all polymers(Φ)and the volume fraction of homopolymer(fC).Rich phase transition sequences were observed,especially reentrant phase transitions,such as lamellae→inverted cylinders→gyroids→lamellae→disorder,for a givenΦwith increasing fC.By analyzing the variations in the average contact numbers between different components and the effective volume fractions of B-domains,we elucidated the mechanisms of the reentrant phase transitions.We found that the strong attraction between B and C leads to the swelling of B-domains upon addition of homopolymer.Concurrently,the solvent preferentially swells the A-domains over the B+C-domains.The competing swelling effects of the solvent and homopolymer on the A-domains and B-domains,respectively,triggered the reentrant phase behavior in the symmetric AB copolymer system upon addition of homopolymer.
基金financially supported by the National Natural Science Foundation of China(Nos.22341304,22303100 and 12205270)the National Key R&D Program of China(Nos.2023YFA1008800 and 2020YFA0713601)the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDC0180303)。
文摘The equilibrium dynamics and nonlinear rheology of unentangled polymer blends remain inadequately understood,especially regarding the influence of short-chain matrix length N_(S) on the structure and rheological behavior of dispersed long chains.Using molecular dynamics simulations based on the Kremer-Grest model,we systematically explore the N_(S)-dependence of static conformations,equilibrium dynamics,and nonlinear shear responses in unentangled long-chain/short-chain polymer blends.Our results demonstrate a decoupling between the static and dynamic sensitivity to N_(S):while the static chain size,R_g,follows Flory theory with slight swelling at small N_(S) due to incomplete excluded volume screening,the diffusion coefficient,D,and the relaxation time,τ_(0),exhibit a strong,non-monotonic N_(S)-dependence,transitioning from monomeric friction dominance at small N_(S) to collective segmental rearrangement at large N_(S).Additionally,we observe partial decoupling between the viscous and normal stress responses:while the zero-shear viscosity,η,is strongly N_(S)-dependent,the first and second normal stress coefficients,Ψ_(1) and Ψ_(2),collapse onto universal curves when scaled by the dimensionless shear rate,γτ_(0),suggesting a common mechanism of orientation and stretching.Under shear,long chains compress in the vorticity direction λ_(z)~Wi^(-0.2),which reduces collision frequency and contributes to shear thinning,while the scaling of weaker orientation resistance m_(G)~Wi^(0.35)reflects hydrodynamic screening by the short-chain matrix.These findings highlight the limitations of single-chain models and emphasize the necessity of considering N_(S)-dependent matrix dynamics and flow-induced structural changes in understanding the rheology of unentangled polymer blends.
文摘Hybrid organic-inorganic perovskites have been the subject of recent intense interest due to advances in photovoltaic and other optoelectronic applications. However, their poor stability limits commercial market application We enhance water stability by post treatment preparation of hybrid metal halide perovskite nanocrystal-embedded polymethylmethacrylate （PM- MA） blend films. Through blending process without any cleaning of nanocrystals, crystalline hybrid organic-inorganic perovs-kite nanocrystals were incorporated into PMMA matrix with well-dispersion Passivation of PMMA on the surface of the per-ovskite nanocrystals results in decreased traps and a long photoluminescence （PL） lifetime despite the bromine vacancies in the crystal lattice. Moreover, such color purity and inherent high transmittance for fluorescence emission of perovskite nanocrystals will endow the films with promising potentials in diverse practice photonic applications.
基金supported by the National High Technology Research and Development Program of China(2010AA101703)the Natural Science Foundation of Heilongjiang Province of China (C200950)the Fundamental Research Fundsfor the Central Universities (DL09BB38)
文摘The effect of maleic anhydride grafted styrene-ethylene- buty-lene-styrene block copolymer （SEBS-g-MAH） and in-situ grafting MAH on mechanical, dynamic mechanical properties of wood flour/recycled plastic blends composites was investigated. Recycled plastic polypro-pylene （PP）, high-density polyethylene （HDPE） and polystyrene （PS）, were mixed with wood flour in a high speed blender and then extruded by a twin/single screw tandem extruder system to form wood flour/recycled plastic blends composites. Results show that the impact properties of the composites were improved more significantly by using SEBS-g-MAH compatibilizer than by using the mixtures of MAH and DCP via reactive blending in situ. However, contrary results were ob-served on the tensile and flexural properties of the corresponding com-posites. In General, the mechanical properties of composites made from recycled plastic blends were inferior to those made from virgin plastic blends, especially in elongation break. The morphological study verified that the interfacial adhesion or the compatibility of plastic blends with wood flour was improved by adding SEBS-g-MAH or in-situ grafting MAH. A better interfacial bonding between PP, HDPE, PS and wood flour was obtained by in-situ grafting MAH than the addition of SEBS-g-MAH. In-situ grafting MAH can be considered as a potential way of increasing the interfacial compatibility between plastic blends and wood flour. The storage modulus and damping factor of composites were also characterized through dynamic mechanical analysis （DMA）.
基金supported by Innovation Research Project for the training of high-level scientific and technological talents(Technical expert talents)of the Armed Police Force ZZKY20222415“13th Five-Year Plan”military key colleges and key disciplines-Equipment Engineering(Power)-17.
文摘Fuel injection properties,including the injection rate(temporal aspects)and spray behavior(spatial aspects),play a crucial role in the combustion efficiency and emissions of diesel engines.This study investigates the effects of different ethanol-biodiesel-diesel(EBD)blends on the injection performance in diesel engines.Experimental tests are conducted to examine key injection parameters,such as spray penetration distance,spray cone angle,and droplet size,alongside an analysis of coupling leakage.The main findings are as follows:(1)The injection behavior of ethanol and diesel differs significantly.The addition of ethanol reduces the density,viscosity,and modulus of elasticity of the fuel mixture.While the injection advance angle,penetration distance,and Sauter mean diameter show minimal changes,the spray cone angle and coupling leakage increase notably.These alterations may disrupt the“fuelair-chamber”matching characteristics of the original engine,potentially affecting performance.(2)In contrast,the injection performance of biodiesel ismore similar to that of diesel.As biodiesel content increases,the density,viscosity,and modulus of elasticity of the blended fuel also grow.Though changes in injection timing,penetration distance,and spray cone angle remain minimal,the Sauter mean diameter experiences a slight increase.The“air-fuel chamber”compatibility of the original engine is largely unaffected,though fuel atomization slightly deteriorates.Blending up to 20%biodiesel and 30%ethanol with diesel effectively compensates for the shortcomings of using single fuels,maintaining favorable injection dynamics while enhancing lubrication and sealing performance of engine components.
文摘Aim To investigate the melting behavior of polyamide 6 in polyamide 6/polyethy lene blends crystallized from amorphous state. Methods DSC was used to test effects of annealing temperature, annealing time, DSC scan rate, and the step wise annealing on the melting peaks of the ice water quenched specimens. Results and Conclusion Varied melting peaks of PA6 component were obtained. The degree of perfection and the crystallization degree of PA6 crystals decreased in the blends, and the crystallization degree of PA6 increased with the increasing of the annealing time. The height of the upper melting peak of reference PA6 is higher than that in blends.
文摘Aim To investigate the multiple melting behavior of polyamide 6(PA 6) in polyamide 6/linear low density polyethylene blends crystallized from the crystal amorphous state. Methods\ The effects of annealing temperature, annealing time, heating rate, and the step wise annealing were measured by DSC. Results and Conclusion\ There exists a critical heating rate affecting the middle temperature melting peak. When annealed at the temperature close to the melting peak, the main melting peak of PA 6 shifted to a higher temperature. Within a short time, annealing time has much effect on neat PA 6 but little effect on PA 6 in the blends. Addition of PE results in a decreasing in the height of melting peak. These phenomenon show that the melting behavior of PA 6 was affected by PE, compatibilizer, as well as thermal treatment.
文摘The thermal behavior of thermotropic hydroxyethyl cellulose acetate (HECA)/polyethylene (PE) blends has been studied by DSC. It is found that the blends of HECA and PE are immiscible but the crystallization of PE is affected by HECA chains in the blends with more than 50% HECA, which results in the subordinate crystallization of PE and the formation of imperfect structures in the PE crystals. The imperfection of PE crystals in the blends can be eliminated after annealing at 393K.
文摘Series of PVC/ABS and PVC/SBS blends of composition 20/ 80. 40/ 60, 60 / 40 and 80 / 20were prepared in a screw extruder. The phase morphology, miscibility and rheological behaviour of two systems were investigated. The viscosity-composition plots were represented by sub-cluster equation, the various differences between two systems are interpreted with the equation parameters
基金financially supported by the Higher Education Commission(HEC),Islamabad,Pakistan under the indigenous Ph D fellowship scheme and IRSIP program
文摘Shape memory polymer （SMP） blends based on polyurethane （PU） and polyaniline （PANI） were prepared via chemical in situ polymerization process. The thermal, mechanical, electrical and shape memory properties were investigated. The structural characterization and morphology of the polymer blends were inspected by Fourier transform infrared （FTIR） and scanning electron microscopy （SEM）, respectively. The 1 wt% of PANI loading enhanced the thermal stability of the system up to 339 ~C. According to differential scanning calorimetry （DSC）, the glass transition temperature （Tg） and melting temperature （Tm） of PU/PANI blends increased with the polyaniline loading （0.1 wt%-l wt%）. Improved mechanical properties such as tensile strength and Young＇s modulus of PU matrix were also observed with PANI. Moreover, the electrical conductivity of PU/PANI blends was also found to be a function of PANI loading. Remarkable recoverability of thermally triggered shape memory （SM） behavior to the extent of 96% was achieved for 1 wt% PANI blend.
基金financially supported by the National Basic Research Program of China(No.2015CB654700(2015CB 654706))Major Program of Shandong Province Natural Science Foundation(No.ZR2017ZA0304)Taishan Scholar Program
文摘The molecular weight of a polymer is of prime importance and greatly influences the processing and mechanical properties of the polymer.Trans-1,4-poly(butadiene-co-isoprene)multi-block copolymer rubbers(TBIR)exhibit outstanding fatigue resistance,low heat build-up and good abrasion resistance,and are expected to be desirable candidate for high performance tire.Study on the influence of TBIR with different molecular weights on the structure and properties of TBIR and natural rubber(NR)/TBIR blends is essential to understand its contribution to the greatly improved dynamic properties of the rubber vulcanizates.TBIR with different molecular weights characterized by 1H-NMR,13C-NMR,GPC,and DSC were highly trans-1,4-copolymers with similar chain sequence distribution and crystalline trans-1,4-polyisoprene(TPI)blocks.The green strength and modulus of TBIR increased with the increasing molecular weight.The NR/TBIR compounds filled with 40 phr carbon black were chemically cured by sulfur for the preparation of NR/TBIR vulcanizates.The compatibility between NR and TBIR,filler distribution,crosslinking bond and density,and properties of NR/TBIR vulcanizates were studied.The NR/TBIR vulcanizates showed increasing tensile strength,hardness,modulus,rebound,abrasion resistance,and flexural fatigue properties with increasing molecular weight of TBIR.Furthermore,they presented significant improvement in flexural fatigue resistance when compared with that of NR vulcanizate.The contribution mechanism of TBIR on the NR/TBIR blends was discussed.The TBIR with a wide range of molecular weight are ideal rubbers for high performance tires.
基金the Chinese Academy of scienee and technology service network planning(No.KFJSTS-QYZD-140)a program of Cooperation of Hubei Province and Chinese Academy of Sciences,Innovation team project of Beijing Institute of Science and Technology(No.IG201703N)"13^th five-year"Science and Technology Research Program of the Education Department of Jilin Provinee(No.JJKH20190862KJ).
文摘Sustainable blends of poly(propylene carbonate)(PPC)and stereocomplex polylactide(sc-PLA)were prepared by melt blending equimolar poly(L-lactic acid)(PLLA)and poly(D-lactide acid)(PDLA)with PPC to form sc-PLA crystals in situ in the melt blending process.Differential seanning calorimetry analysis revealed that only sc-PLA,no homo-crystallization of PLLA or PDLA,formed in the PPC matrix as the sc-PLA con tent was more than 10 wt%.Very in triguingly,scan ning electronic microscopy observati on showed that sc-PLA was evenly dispersed in the PPC phase as spherical particles and the sizes of sc-PLA particles did not obviously increase with in creasing sc-PLA con tent.As a con seque nee,the rheological properties of PPC were greatly improved by incorporation of sc-PLA.When the sc-PLA con tent was 20 wt%,a percolati on n etwork structure was formed,and the blends showed solid-like behavior.The sc-PLA particles could reinforce the PPC matrix,especially at a temperature above the glass transition temperature of PPC.Moreover,the Vicat softening temperature of PPC/sc-PLA blends could be increased compared with that of neat PPC.
基金financially supported by the fund of Science&Technology Bureau of Jilin Province of China(No.20126023)the National High Technology Research and Development Program of China(863 Program)(No.2012AA062904)the National Natural Science Foundation of China(No.51021003)
文摘Poly（propylene carbonate） （PPC） was melt blended in a batch mixer with poly（butylene carbonate） （PBC） in an effort to improve the toughness of the PPC without compromising its biodegradability and biocompatibility. DMA results showed that the PPC/PBC blends were an immiscible two-phase system. With the increase in PBC content, the PPC/PBC blends showed decreased tensile strength, however, the elongation at break was increased to 230% for the 50/50 PPC/PBC blend. From the tensile strength experiments, the Pukanszky model gave credit to the modest interfacial adhesion between PPC and PBC, although PPC/PBC was immscible. The impact strength increased significantly which indicated the toughening effects of the PBC on PPC. SEM examination showed that cavitation and shear yielding were the major toughening mechanisms in the blends subjected the impact tests. TGA measurements showed that the thermal stability of PPC decreased with the incorporation of PBC. Rheological investigation demonstrated that the addition of PBC reduced the value of storage modulus, loss modulus and complex viscosity of the PPC/PBC blends to some extent. Moreover, the addition of PBC was found to increase the processability of PPC in extrusion. The introduction of PBC provided an efficient and novel toughened method to extend the application area of PPC.
基金supported by the National Natural Science Foundation of China(Nos.50533050,20874064 and 50873063)
文摘A simultaneous increase of both stiffness and extensibility ofpoly（ethylene glycol-co-cyclohexane-1,4-dimethanol terephthalate） （PETG）/polycarbonate （PC） blends prepared through the slit die extrusion-uniaxial cold stretching process was observed. The stretched sheets have a unique mechanical character that an increased tensile modulus is accompanied by an increased extensibility with increasing the draw ratio. Especially, a sharp increasing of the extensibility is observed for PETG/PC （70/30 wt%） blends at draw ratios between 8.2 and 20.0, where a nine times increase of extensibility is achieved. The mechanism of stretching-induced superior extensibility is investigated via micrograph observation, rheometry and calorimetric analysis. The observed superior extensibility could be tentatively explained by the bridging effect of the PC microfibrils on the crack development during tensile failure.
基金This work was financially supported by the Special Funds for Major State Basic Research Projects of China (No.2005CB623800)the National Natural Science Foundation of China (No. 20374037)the Open Foundation of Key Laboratory of Rubber-plastics (QUST),Ministry of Education, China and the Foundation for Youth of Sichuan University
文摘Metallocene-catalyzed linear low-density polyethylene/polypropylene （mLLDPE/PP） blends were prepared by ultrasonic extrusion in this work. Their extrusion processing behaviors were estimated by online measured data, such as the die pressure and flow rate. Crystallization and mechanical properties of the blends were also investigated. The results show that the addition of PP improves the processing behaviors of mLLDPE, but has little effect on its mechanical properties. On the other hand, the addition of mLLDPE improves the impact strength of PP, but has little effect on its processing behavior. The processing behaviors and mechanical properties of mLLDPE/PP blends get further improved due to the presence of ultrasonic oscillation during extrusion. Compared with PP-rich blends, the apparent viscosity drop of mLLDPE-rich blends is more sensitive to ultrasonic oscillation. The ultrasonic oscillation affects the crystal nucleation, while barely the other crystalline behaviors of the blends.
文摘Phase separation was studied by the optical microscopy in blends of nylon 6 (PA6) with sodium salt of ethylene/methacrylic acid copolymer (PEMA).The image collecting technology was used to keep track of the development of blends at a certain temperature.The fractal dimension of phase separation was calculated by the image solving technology according to the fractal theory and the self similarity behavior of the process was proved.The relationship of the fractal behavior with composition and experimental temperature was discussed.The fractal behavior of the crystallization development of the crystal phase of PA6 in blends was also discussed and the fractal behavior calculated.
基金financially supported by the National Natural Science Foundations of China(No.20974011)the program of Introducing Talents of Discipline to Universities(No.B08003)
文摘The effect of PBS on the morphological features of PVDF has been investigated by optical and atomic force microscopies under various conditions. It was found that neat PVDF forms large γform spherulites with extraordinarily weak birefringence at 170℃. Adding 30% PBS makes PVDF exhibit intrigued flower-like spherulitic morphology. The growth mechanism was explained by the decrease of the supercooling and the materials dissipation. Increasing the PBS content to 70% favors the formation of ring banded spherulites. Temperature dependent experiments verify the α→γ phase transition occurs from the junction sites of the ot and y crystals, while starts from the centers of α spherulites in the blends. Ring banded structures could be observed in neat PVDF, 70/30 blend and 30/70 blend when crystallized at 155℃, without γ crystals. The band period of PVDF α spherulites increases with crystallization temperature as well as the amount of PBS content. At 140℃, spherulites in neat PVDF lose their ring banded feature, while coarse spherulites consisting of evident lamellar bundles could be found in 30/70 blend.
文摘In this work, polypropylene (PP)/polystyrene (PS) blends with different organoclay concentrations were prepared via melt compounding. Differing from the results of previous reports, the organoclay platelets are mostly located in the dispersed PS phase instead of the interface. The dimensions of the dispersed PS droplets are greatly reduced and apparent compatibilization effect still exists, which cannot be explained by the traditional compatibilization mechanism. A novel compatibilization mecha- nism, "cutting" to apparently compatibilize the immiscible PP/PS blends was proposed. The organoclay platelets tend to form a special "knife-like structure" in the PS domain under the shear stress of the continuous PP phase during compounding. The "clay knife" can split the dispersed PS domain apart and lead to the dramatic reduction of the dispersed domain size.
