Starch- g-poly(vinyl alcohol) as a compatibilizing agent for reducing the phase separation rates of polyvinyl alcohol/starch pastes has been investigated by blending and dissolving the two polymers in distilled water....Starch- g-poly(vinyl alcohol) as a compatibilizing agent for reducing the phase separation rates of polyvinyl alcohol/starch pastes has been investigated by blending and dissolving the two polymers in distilled water. The separation rates were quantitatively evaluated by the term of initiul demixing time. The grafted starches, with a series of grafting ratios, were prepared by grafting a number of vinyl acetate onto granular cornstarch in aqueous dispersion and then alcoholating in methanol. It was found that the addition of small amounts of starch- g poly (vinyl alcohol ) in the size compositions can effectively decrease the separation rates of the blended pastes in comparison to pure starch/PVA ones.Moreover, the influence of the grafting ratio, starch content, and PVA variety on the separation rates was also studied.展开更多
Low density polyethylene(LDPE)/lignin blends were prepared using melt blending.Two kinds of compatibilizers, ethylene-vinylacetate(EVA) which is softer than LDPE and polyethylene grafted with maleic anhydride(PE-g-MA)...Low density polyethylene(LDPE)/lignin blends were prepared using melt blending.Two kinds of compatibilizers, ethylene-vinylacetate(EVA) which is softer than LDPE and polyethylene grafted with maleic anhydride(PE-g-MA) which is harder than LDPE were used to improve the interfacial adhesion.Scanning electron microscope(SEM) was used to investigate the dispersion of lignin in LDPE matrix.The results showed that both of the compatibilizers could improve the interaction between the low density polyethylene an...展开更多
Recycled PET (R-PET) is well known to exhibit brittle behavior in the presence of notches and indicated the low heat distortion temperature. In addition, it is hard to prevent some impurities such as cap or label of t...Recycled PET (R-PET) is well known to exhibit brittle behavior in the presence of notches and indicated the low heat distortion temperature. In addition, it is hard to prevent some impurities such as cap or label of the bottle that mixed into R-PET during the recycling process. In this paper, the effect of the amounts and kinds of compatibilizers on the morphological characteristics and mechanical performance of recycled poly(ethylene terephthalate) (R-PET) compounded with polyethylene (PE), polypropylene (PP), and polystyrene (PS) was investigated. From the results, with an increase in the glycidyl methacrylate modified PE (EGMA) additive contents, in the increment of the Izod impact strength of Composite-G was obtained. In addition, it was found that the miscibility of Composite-G was improved with increasing the amount of EGMA, which indicated from the result of SEM images.展开更多
In situ compatibilization of low density polyehylene (LDPE) (30%) and nylon-6(70%)blends through one-step reactive extrusion using t-BuOOH as an initiator and low molec-ular weight interfacial agents as compatibilizer...In situ compatibilization of low density polyehylene (LDPE) (30%) and nylon-6(70%)blends through one-step reactive extrusion using t-BuOOH as an initiator and low molec-ular weight interfacial agents as compatibilizers was studied. The compatibilizer containeda long chain bydrocarbon, double bond and two polar functional groups which was capableof reacting with both LDPE and nylon-6 in the presence of initiator to form a copolymerat the interface of the two polymer phases. The extruded blends exhibited significant en-hancement in their compatibility based on morphological, thermal analysis and mechanicalstudies. The effect of the hydrocarbon chain length and structure of the functional groupof the compatibilizer was also examined. It was found that blends prepared by using thecompatibilizer containing longer hydrocarbon chain and amide group had better mechanicalproperties.展开更多
The compatibilizer (TLCP-b-PC) of 60PHB/PET thermotropic liquid crystal polymer (TLCP) and polycarbonate (PC) blend system was prepared. The synthesis and characterization of the compatibilizer as well as its effects ...The compatibilizer (TLCP-b-PC) of 60PHB/PET thermotropic liquid crystal polymer (TLCP) and polycarbonate (PC) blend system was prepared. The synthesis and characterization of the compatibilizer as well as its effects on the microscopic morphology and the mechanical properties of the TLCP/PC blend system were studied with a series of analysis ways, such as Soxhlet extraction, infrared absorption spectroscopy,electron microscopy, etc. It is shown that the ideal reaction condition for preparing the compatibilizer is:the reaction temperature of 275℃, the reaction time of 20minutes and without catalyst. And the compatibilizer can improve the compatibility of the blending system of 60PHB/PET and PC.展开更多
Adding compatibilizer to polymer-modified asphalt(PMA)is an effective method to improve compatibility and performance.However,only few studies have systematically focused on how compatibilizer can affect the performan...Adding compatibilizer to polymer-modified asphalt(PMA)is an effective method to improve compatibility and performance.However,only few studies have systematically focused on how compatibilizer can affect the performance of styrene-butadiene-styrene(SBS)polymer-modified asphalt(PMA).In this study,six compatibilizers with different compositions were used to prepare SBS PMA samples.Conventional performance,viscosity-temperature characteristics,viscoelastic behavior,creep properties,and morphology were investigated.The results show that adding compatibilizer to SBS PMA has a great effect on its performance.High aromatics content in compatibilizers can improve the high-temperature performance of SBS PMA,while a high saturates content can enhance the low-temperature performance.Additionally,high aromatics content in compatibilizer can increase the temperature sensitivity.While the aromatics content does improve the compatibility of SBS PMA to some extent,adding compatibilizer to SBS PMA has few effects on the microstructure.Judging from our test results,we can conclude that the optimum aromatics content for adding compatibilizer to SBS PMA ranges from 33.21%to 54.22%.展开更多
Two compatibilizers consisting of styrene-acrylonitrile-glycidyl methacrylate (SAG) terpolymer with different contents of glycidyl methacrylate (GMA), SAG-001 (1 wt% of GMA) and SAG-005 (5 wt% of GMA), and styrene-acr...Two compatibilizers consisting of styrene-acrylonitrile-glycidyl methacrylate (SAG) terpolymer with different contents of glycidyl methacrylate (GMA), SAG-001 (1 wt% of GMA) and SAG-005 (5 wt% of GMA), and styrene-acry-lonitrile-maleic anhydride terpolymer (SAM), SAM-002 (2 wt% of maleic anhydride ), were used to evaluate the role of compatibilizers in the PC/ABS alloy in terms of the mechanical properties, thermal stability and phase morphology. The tensile strength of SAG modified PC/ABS alloy slightly increased than that of SAM modified system, but the two compatibilizers barely affected the flexural strength of the system. On the other hand, the impact strength of SAG modified PC/ABS was improved. In addition, the MFR (melt flow index) of the SAG modified PC/ABS alloy reduced, implying that the viscosity or molecular weight of the system increased. The HDT (heat distortion temperature) also improved with SAG modified system. Moreover, the phase morphology of the SAG modified PC/ABS alloys much enhanced than that of SAM modified system. As a consequence, SAG compatibilized PC/ABS alloy showed better properties than those of SAM modified system, suggesting that the reaction between carboxylic or epoxy groups in SAG and terminal carboxyl group in PC would be the main factor to bring the enhancement in the mechanical, thermal and morphological properties of the PC/ABS alloy.展开更多
The effect of R-styrene-maleic anhydride copolymer(R-SMA) compatibilzation on Nylon 6(PA6)/polypropylene(PP) blends has been investigated experimentally through Molau test,microscopic morphology,and chemical structure...The effect of R-styrene-maleic anhydride copolymer(R-SMA) compatibilzation on Nylon 6(PA6)/polypropylene(PP) blends has been investigated experimentally through Molau test,microscopic morphology,and chemical structure.Results show that the moderate R-SMA addition can promote reaction between anhydride in R-SMA and amino in PA6,and lead to a new PA6-g-R-SMA copolymer in the blends.Such PA6-g-R-SMA copolymer in the blends can effectively reduce the interfacial tension and PP particle size,and improve the compatibility of two immiscible phases in the blends.The crystallinity of PA6 in PA6/PP blends has greatly decreased by PP blends.The blends have the best comprehensive mechanical and thermal properties when the mass ratio of PA6/PP/R-SMA is 90:10:2 to 90:10:4.The impact strength of the PA6/PP blends with the compatibilizer is increased by more than 150%.展开更多
Poly(butylene adipate-co-terephthalate) (PBAT) is currently the largest commercial biodegradable plastics with good toughness and film forming properties, whereas, the inferior barrier and mechanical properties hinder...Poly(butylene adipate-co-terephthalate) (PBAT) is currently the largest commercial biodegradable plastics with good toughness and film forming properties, whereas, the inferior barrier and mechanical properties hinder its applications. Biodegradable poly(propylene carbonate) (PPC) with excellent barrier properties and high strength is a natural choice to address above issue. However, it is challenging to improve the compatibility of these two polymers. Herein, we prepared a reactive compatibilizer with double bond side group through terpolymerization of CO_(2)/propylene oxide/glycidyl methacrylate to enhance the properties of PBAT/PPC blends. Upon addition of 1 wt% compatibilizer, the PBAT/PPC blends (75/25, W/W) showed an increased water vapor barrier property changed from 424 g·m^(−2)·d^(−1) to 204 g·m^(−2)·d^(−1) compared to the control sample. Moreover, the tensile strength and elongation at break increased from 24.7 MPa to 30.3 MPa and from 858% to 1142%, respectively. The PBAT/PPC composite also displayed excellent biodegradability under composting conditions, as confirmed by the significantly decreased molecular weight. The present work provides an efficient way to barrier biodegradable film from PBAT of practical utilization.展开更多
Mixing two or more polymers to produce the“polymer alloy”is one of the most versatile and economical strategies for developing new polymeric materials.The compatibility between polymer components largely determines ...Mixing two or more polymers to produce the“polymer alloy”is one of the most versatile and economical strategies for developing new polymeric materials.The compatibility between polymer components largely determines the comprehensive performance of polymer blend.More recently,a type of unique surface partitioned materials,Janus particles,has been proposed to act as a novel interfacial compatibilizer for polymer blends.Such Janus particles integrates the amphipathicity of diblock copolymer and interfacial stabilization of nanoparticles,displaying a significant superiority in comparison with molecular compatibilizers for a wide range of polymer blends.In this review,we mainly focus on the compatibilizing effects of Janus nanofillers of various morphologies,including spherical,snowman-like,and two-dimensional nanosheets,on polymer blends.We shed light on the impacts of compatibilization of Janus particles on phase morphologies,mechanical properties,and functionalities of polymer blends.This review could provide a guidance for designing an effective Janus particle compatibilizer to develop high-performance polymer blends.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
Polyamide/acrylonitrile-butadiene-styrene copolymer(PA/ABS) blends have drawn considerable attention from both academia and industry for their important applications in automotive and electronic areas. Due to poor mis...Polyamide/acrylonitrile-butadiene-styrene copolymer(PA/ABS) blends have drawn considerable attention from both academia and industry for their important applications in automotive and electronic areas. Due to poor miscibility of PA and ABS, developing an effective compatibilization strategy has been an urgent challenge to achieve prominent mechanical properties. In this study, we create a set of mechanically enhanced PA6/ABS blends using two multi-monomer melt-grafted compatibilizers, SEBSg-(MAH-co-St) and ABS-g-(MAH-co-St). The dispersed domain size is significantly decreased and meanwhile the unique "soft shell-encapsulating-hard core" structures form in the presence of compatibilizers. The optimum mechanical performances manifest an increase of 36% in tensile strength and an increase of 1300% in impact strength, compared with the neat PA6/ABS binary blend.展开更多
Donor-acceptor(D-A) type fully conjugated block copolymer systems have been rarely reported due to the challenges in synthetic approaches to prepare well-defined low-polydispersity products. In this work, fully conjug...Donor-acceptor(D-A) type fully conjugated block copolymer systems have been rarely reported due to the challenges in synthetic approaches to prepare well-defined low-polydispersity products. In this work, fully conjugated block copolymers are synthesized in a one-pot reaction through Stille coupling polycondensation, by utilizing the end-functional polymer copolymerization method. End-functional P3HT are copolymerized with AA(2,7-dibromo-9-(heptadecan-9-yl)-9Hcarbazole) and BB(4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole, TBT) type monomers, respectively. The orthogonal solubility between the very soluble P3HT donor and the insoluble PCDTBT acceptor block improves the purity of block copolymers as well as distinct nano-scale phase-separation compared with other reports on miscibility of donor and acceptor polymer block. Further purification via preparative GPC is carried out to remove the excess of unreacted P3HT and free PCDTBT as well as to achieve low polydispersity of block copolymers. The chemical structure of the P3HTb-PCDTBT block copolymers are verified via ~1H-NMR, and further confirmed by FTIR spectra. The block copolymer shows broad absorption and moderate optical band gap of 1.8 e V. Furthermore, the fully conjugated block copolymer films exhibit significant fine structures, much smoother film morphology compared to P3HT/PCDTBT polymer blends. By adding a small amount of block copolymer P3HT-b-PCDTBT as a compatibilizer into the bulk-heterojunction of P3HT:PC_(61)BM blends, polymer solar cells with an 8% increase of short circuit current(J_(sc)) and 10% increase of power conversion efficiency(PCE) are achieved owing to the improvement of the active-layer film morphology. To the best of our knowledge, this is the first report on donor-acceptor type fully conjugated block copolymer as an effective ternary additive in polymer: fullerene bulk heterojunction solar cells.展开更多
In this work,the formation of cocontinuous structure in immiscible high density polyethylene/isotactic polypropylene(HDPE/iPP)blends was investigated for various olefin-based compatibilizers of distinct molecular arch...In this work,the formation of cocontinuous structure in immiscible high density polyethylene/isotactic polypropylene(HDPE/iPP)blends was investigated for various olefin-based compatibilizers of distinct molecular architectures,including ternary random copolymer EPDM,olefin block copolymer(OBC),polypropylene-based OBC(PP-OBC),ethylene/a-olefin copolymer(POE),bottlebrush polymer poly(1-dodecene),and comb-like poly(propylene-co-high a-olefin)(PPO).The scanning electron microscopy results show that after adding OBC,PP-OBC,and POE copolymers,the finer droplet-in-matrix morphologies were obtained in 70/30 HDPE/iPP blend.Interestingly,for 70/30 HDPE/iPP blend with just 5 wt%of PPO copolymers,the phase inversion from droplet-in-matrix to cocontinuous morphology can be observed.It was proposed that the development of cocontinuous morphology contained the following steps:(1)in terfacial saturati on of compatibilizers and droplet deformation,(2)droplet-droplet coalesce nee,(3)continuity development,and(4)the formation of dual-phase con tinuity.Among the diverse copolymers studied in this work,PPO copolymer can be easily removed out of the interface during droplet coalescence and stabilize the curvature of minor fiber phase,facilitating the formation of cocontinuous morphology.In contrast,other olefin-based compatibilizers(EPDM,OBC,PP-OBC,and POE)exhibit the distinct steric repulsion effect to prohibit droplet coalescence.Moreover,the cocontinous interval varies with the compatibilizer architectures.Surprisingly,after adding 10 wt%of PPO copolymers,the cocontinuous interval was greatly broadened from HDPE/iPP range of 45/55-60/40 to that of 40/60-70/30.展开更多
The objective of this study was to improve the toughness of bio based brittle poly(ethylene 2,5-furandicarboxylate)(PEF)by melt blending with bio based polyamide11(PA11)in the presence of a reactive multifunctional ep...The objective of this study was to improve the toughness of bio based brittle poly(ethylene 2,5-furandicarboxylate)(PEF)by melt blending with bio based polyamide11(PA11)in the presence of a reactive multifunctional epoxy compatibilizer(Joncryl ADR-4368).The morphological,thermal,rheological,and mechanical properties of PEF/PA11 blends were investigated.Compared with neat PEF,the toughness of PEF/PA11 blend was not improved in the absence of the reactive compatibilizer due to the poor compatibility between the two polymers.When Joncryl was incorporated into PEF/PA11 blends,the interfacial tension between PEF and PA11 was obviously reduced,reflecting in the fine average particle size and narrow distribution of PA11 dispersed phase as observed by scanning electron microscopy(SEM).The complex viscosities of PEF/PA11 blends with Joncryl were much higher than that of PEF/PA11 blend,which could be ascribed to the formation of graft copolymers through the epoxy groups of Joncryl reacting with the end groups of PEF and PA11 molecular chains.Thus,the compatibility and interfacial adhesion between PEF and PA11 were greatly improved in the presence of Joncryl.The compatibilized PEF/PA11 blend with 1.5 phr Joncryl exhibited significantly improved elongation at break and unnotch impact strength with values of 90.1%and 30.3kJ/m2,respectively,compared with those of 3.6%and 3.8 kJ/m2 for neat PEF,respectively.This work provides an effective approach to improve the toughness of PEF which may expand its widespread application in packaging.展开更多
Poly(butylene adipate-co-terephthalate)(PBAT)and poly(butylene succinate-co-adipate)(PBSA)blend films were prepared with different contents of a multifunctional epoxide chain extender Joncryl ADR-4468(ADR)or benzoyl p...Poly(butylene adipate-co-terephthalate)(PBAT)and poly(butylene succinate-co-adipate)(PBSA)blend films were prepared with different contents of a multifunctional epoxide chain extender Joncryl ADR-4468(ADR)or benzoyl peroxide(BPO).The long-chain-branching(LCB)introduced by ADR and branched/crosslinked entanglement induced by BPO increased melt elasticity,viscosity and compatibility,as indicated by thermal properties,rheological and morphological analyses.It was found that the elongation at break and the tensile strength were significantly improved,due to the enhancement of compatibility and the interfacial adhesion by the incorporation of ADR or BPO.The best mechanical properties were obtained in PBAT/PBSA/ADR(60/40/0.3)(A4T6A_(0.3))and PBAT/PBSA/BPO(60/40/0.9)(A4T6B_(0.9))films,respectively.With the rapid initiation of chain growth by BPO,it has significantly improved the transparency of the film.ADR and BPO can be used interchangeably in improving the comprehensive properties of PBAT/PBSA films,and it would provide more strategies for developing biodegradable materials for various applications.展开更多
Blend of natural rubber (NR) and chlorosulfonated polyethylene (CSM) was so interesting due to binding of the good oil resistance of CSM, the good mechanical properties and low cost of NR. However, due to the differen...Blend of natural rubber (NR) and chlorosulfonated polyethylene (CSM) was so interesting due to binding of the good oil resistance of CSM, the good mechanical properties and low cost of NR. However, due to the different polarities of two rubbers, phase separation and inferior properties of NR/CSM blend were obtained. The practical way to improve its properties is the addition of the third component to bind both phases of the blend. Effects of poly(vinyl chloride), PVC as compatibilizer on cure characteristics, morphology, mechanical properties and automotive fuel resistance of NR/ CSM blend were investigated. In this contribution, NR/CSM blend with blend ratio of 50/50 was prepared using a two-roll mill, and then vulcanized in a compression mold at 160°C. The PVC content was varied from 1 to 7 phr. It was found that the usage of 7 phr PVC led to improve interaction between NR and CSM phases. Therefore, increase in cure characteristics, mechanical strength and automotive fuel resistance of the blend was observed.展开更多
The mechanical properties of composites prepared from wood flour and thermoplastic blends were investigated. Thermoplastic mixtures of polypropylene (PP) and high-density polyethylene (HDPE) and polystyrene (PS), virg...The mechanical properties of composites prepared from wood flour and thermoplastic blends were investigated. Thermoplastic mixtures of polypropylene (PP) and high-density polyethylene (HDPE) and polystyrene (PS), virgin or recycled, were mixed with wood flour in a high speed blender and then extruded by a specially designed twin/single screw extruder system to form wood-flour/thermoplastic-blends composites (WTBCs). Comparative studies were made to evaluate the effectiveness of the two modification methods of the thermoplastic blends, the one of the addition of maleic anhydride grafted styrene-ethylene-butylene-styrene block copolymer (SEBS-g-MAH) as compatibilizer and the other of blend grafting of maleic anhydride (MAH) using dicumyl peroxide (DCP) as initiator by reactive extrusion. The results showed that the impact properties of WTBCs using SEBS-g-MAH as compatilizer were better improved than that of the blend grafting. However, adverse results were observed on the tensile and flexural properties of the corresponding WTBCs. The mechanical properties of WTBCs prepared from recycled plastic blends were poorer to some extent than that from virgin plastic blends in general, especially in elongation break. The morphology of WTBCs breaking section was analyzed by scanning electron microscopy (SEM) and the results showed that a good interfacial adhesion between wood flour and polymer matrix was observed with both of the two modification methods. However, by blend grafting of adding DCP as initiator and MAH as monomer, a better interfacial bonding between wood and plastic matrix was obtained than that of the addition of SEBS-g-MAH. Blend grafting can be considered as a potential way of increasing the interfacial compatibility of different plastics and between plastic blends and wood.展开更多
An amphiphilic graft polymer, (PAM-g-PBA), polyacrylamide (PAM) having poly(n-butyl acrylate) (PBA) side chains, was obtained by radical copolymerization of acrylamide with PBA macromer in solution. The macromer was s...An amphiphilic graft polymer, (PAM-g-PBA), polyacrylamide (PAM) having poly(n-butyl acrylate) (PBA) side chains, was obtained by radical copolymerization of acrylamide with PBA macromer in solution. The macromer was synthesized by free radical polymerization of butyl acrylate in the presence of different amounts of thioglycolic acid as the chain transfer agent, followed by termination with glycidyl methacrylate. The reactivity ratio and effects of copolymerization conditions on the conversion of macromer or grafting efficiency were studied. The crude products were purified by extraction with toluene and water successively. The purified graft copolymer was characterized by IR, DSC and TEM. PAM-g-PBA can bring about microphase separation and exhibits good emulsifying properties and water absorbency. PAM-g-PBA exhibits a very good compatibilizing effect on the acrylic rubber/poly(vinyl chloride) blends. 2%-3% of the graft copolymer is enough for enhancing the tensile strength of the blends. The tensile strength of the blends is more than twice that without the compatibilizer. DSC and SEM demonstrated the enhancement of compatibility in the presence of the graft copolymer.展开更多
The alloy of Nylon 6/acrylonitrile-butadiene-styrene(ABS)was used for a compatibilizer to generate the maleic anhydride(ABS-g-MAH),in which the proportion of PA6/ABS is 90/10.The results of the mechanical tests show t...The alloy of Nylon 6/acrylonitrile-butadiene-styrene(ABS)was used for a compatibilizer to generate the maleic anhydride(ABS-g-MAH),in which the proportion of PA6/ABS is 90/10.The results of the mechanical tests show that when the content of ABS-g-MAH is 20%,the impact strength of the alloy with the compatibilizer increased by around 41%,compared with that of the PA6/ABS alloy;Besides,the tensile strength has been significantly improved.Furthermore,in accordance with the dynamic mechanical analysis,α relaxation temperature of Nylon 6 has raised from 70 ℃ to 110 ℃ with the addition of ABS and ABS-g-MAH;moreover,and the obvious relaxations of β and γ occur at about 60 ℃ and-60 ℃,respectively.It can be seen from the scanning electron microscope(SEM)photographs that the compatibility has been improved through the addition of ABS-g-MAH.The water absorption of Nylon 6 has also been improved by the addition of ABS and ABS-g-MAH.When the content of ABS-g-MAH is 10%,the water absorption of the alloy will fall by 50%.展开更多
基金It was financially supported by China Postdoctoral Science Foundation[1995]No.7
文摘Starch- g-poly(vinyl alcohol) as a compatibilizing agent for reducing the phase separation rates of polyvinyl alcohol/starch pastes has been investigated by blending and dissolving the two polymers in distilled water. The separation rates were quantitatively evaluated by the term of initiul demixing time. The grafted starches, with a series of grafting ratios, were prepared by grafting a number of vinyl acetate onto granular cornstarch in aqueous dispersion and then alcoholating in methanol. It was found that the addition of small amounts of starch- g poly (vinyl alcohol ) in the size compositions can effectively decrease the separation rates of the blended pastes in comparison to pure starch/PVA ones.Moreover, the influence of the grafting ratio, starch content, and PVA variety on the separation rates was also studied.
基金supported by the National Natural Science Foundation of China(Nos.50533050,20634050)
文摘Low density polyethylene(LDPE)/lignin blends were prepared using melt blending.Two kinds of compatibilizers, ethylene-vinylacetate(EVA) which is softer than LDPE and polyethylene grafted with maleic anhydride(PE-g-MA) which is harder than LDPE were used to improve the interfacial adhesion.Scanning electron microscope(SEM) was used to investigate the dispersion of lignin in LDPE matrix.The results showed that both of the compatibilizers could improve the interaction between the low density polyethylene an...
文摘Recycled PET (R-PET) is well known to exhibit brittle behavior in the presence of notches and indicated the low heat distortion temperature. In addition, it is hard to prevent some impurities such as cap or label of the bottle that mixed into R-PET during the recycling process. In this paper, the effect of the amounts and kinds of compatibilizers on the morphological characteristics and mechanical performance of recycled poly(ethylene terephthalate) (R-PET) compounded with polyethylene (PE), polypropylene (PP), and polystyrene (PS) was investigated. From the results, with an increase in the glycidyl methacrylate modified PE (EGMA) additive contents, in the increment of the Izod impact strength of Composite-G was obtained. In addition, it was found that the miscibility of Composite-G was improved with increasing the amount of EGMA, which indicated from the result of SEM images.
文摘In situ compatibilization of low density polyehylene (LDPE) (30%) and nylon-6(70%)blends through one-step reactive extrusion using t-BuOOH as an initiator and low molec-ular weight interfacial agents as compatibilizers was studied. The compatibilizer containeda long chain bydrocarbon, double bond and two polar functional groups which was capableof reacting with both LDPE and nylon-6 in the presence of initiator to form a copolymerat the interface of the two polymer phases. The extruded blends exhibited significant en-hancement in their compatibility based on morphological, thermal analysis and mechanicalstudies. The effect of the hydrocarbon chain length and structure of the functional groupof the compatibilizer was also examined. It was found that blends prepared by using thecompatibilizer containing longer hydrocarbon chain and amide group had better mechanicalproperties.
文摘The compatibilizer (TLCP-b-PC) of 60PHB/PET thermotropic liquid crystal polymer (TLCP) and polycarbonate (PC) blend system was prepared. The synthesis and characterization of the compatibilizer as well as its effects on the microscopic morphology and the mechanical properties of the TLCP/PC blend system were studied with a series of analysis ways, such as Soxhlet extraction, infrared absorption spectroscopy,electron microscopy, etc. It is shown that the ideal reaction condition for preparing the compatibilizer is:the reaction temperature of 275℃, the reaction time of 20minutes and without catalyst. And the compatibilizer can improve the compatibility of the blending system of 60PHB/PET and PC.
基金This work was supported by the Fundamental Research Funds for the Central Universities(B210202040)the National Natural Science Foundation of China(51708177).
文摘Adding compatibilizer to polymer-modified asphalt(PMA)is an effective method to improve compatibility and performance.However,only few studies have systematically focused on how compatibilizer can affect the performance of styrene-butadiene-styrene(SBS)polymer-modified asphalt(PMA).In this study,six compatibilizers with different compositions were used to prepare SBS PMA samples.Conventional performance,viscosity-temperature characteristics,viscoelastic behavior,creep properties,and morphology were investigated.The results show that adding compatibilizer to SBS PMA has a great effect on its performance.High aromatics content in compatibilizers can improve the high-temperature performance of SBS PMA,while a high saturates content can enhance the low-temperature performance.Additionally,high aromatics content in compatibilizer can increase the temperature sensitivity.While the aromatics content does improve the compatibility of SBS PMA to some extent,adding compatibilizer to SBS PMA has few effects on the microstructure.Judging from our test results,we can conclude that the optimum aromatics content for adding compatibilizer to SBS PMA ranges from 33.21%to 54.22%.
文摘Two compatibilizers consisting of styrene-acrylonitrile-glycidyl methacrylate (SAG) terpolymer with different contents of glycidyl methacrylate (GMA), SAG-001 (1 wt% of GMA) and SAG-005 (5 wt% of GMA), and styrene-acry-lonitrile-maleic anhydride terpolymer (SAM), SAM-002 (2 wt% of maleic anhydride ), were used to evaluate the role of compatibilizers in the PC/ABS alloy in terms of the mechanical properties, thermal stability and phase morphology. The tensile strength of SAG modified PC/ABS alloy slightly increased than that of SAM modified system, but the two compatibilizers barely affected the flexural strength of the system. On the other hand, the impact strength of SAG modified PC/ABS was improved. In addition, the MFR (melt flow index) of the SAG modified PC/ABS alloy reduced, implying that the viscosity or molecular weight of the system increased. The HDT (heat distortion temperature) also improved with SAG modified system. Moreover, the phase morphology of the SAG modified PC/ABS alloys much enhanced than that of SAM modified system. As a consequence, SAG compatibilized PC/ABS alloy showed better properties than those of SAM modified system, suggesting that the reaction between carboxylic or epoxy groups in SAG and terminal carboxyl group in PC would be the main factor to bring the enhancement in the mechanical, thermal and morphological properties of the PC/ABS alloy.
基金Science and Technology Program from Jiangxi Provincial Department of Education,China (No. CJJ10377)
文摘The effect of R-styrene-maleic anhydride copolymer(R-SMA) compatibilzation on Nylon 6(PA6)/polypropylene(PP) blends has been investigated experimentally through Molau test,microscopic morphology,and chemical structure.Results show that the moderate R-SMA addition can promote reaction between anhydride in R-SMA and amino in PA6,and lead to a new PA6-g-R-SMA copolymer in the blends.Such PA6-g-R-SMA copolymer in the blends can effectively reduce the interfacial tension and PP particle size,and improve the compatibility of two immiscible phases in the blends.The crystallinity of PA6 in PA6/PP blends has greatly decreased by PP blends.The blends have the best comprehensive mechanical and thermal properties when the mass ratio of PA6/PP/R-SMA is 90:10:2 to 90:10:4.The impact strength of the PA6/PP blends with the compatibilizer is increased by more than 150%.
基金supported by National Key Research and Development Program of China (No. 2021YFD1700700).
文摘Poly(butylene adipate-co-terephthalate) (PBAT) is currently the largest commercial biodegradable plastics with good toughness and film forming properties, whereas, the inferior barrier and mechanical properties hinder its applications. Biodegradable poly(propylene carbonate) (PPC) with excellent barrier properties and high strength is a natural choice to address above issue. However, it is challenging to improve the compatibility of these two polymers. Herein, we prepared a reactive compatibilizer with double bond side group through terpolymerization of CO_(2)/propylene oxide/glycidyl methacrylate to enhance the properties of PBAT/PPC blends. Upon addition of 1 wt% compatibilizer, the PBAT/PPC blends (75/25, W/W) showed an increased water vapor barrier property changed from 424 g·m^(−2)·d^(−1) to 204 g·m^(−2)·d^(−1) compared to the control sample. Moreover, the tensile strength and elongation at break increased from 24.7 MPa to 30.3 MPa and from 858% to 1142%, respectively. The PBAT/PPC composite also displayed excellent biodegradability under composting conditions, as confirmed by the significantly decreased molecular weight. The present work provides an efficient way to barrier biodegradable film from PBAT of practical utilization.
基金the National Natural Science Foundation of China (Nos. 52173076 and 52042302)China Postdoctoral Science Foundation (No. 2021M701825)+1 种基金Tsinghua-Foshan Innovation Special Fund (TFISF) (No. 2021THFS0212)Joint Agency Affiliate Projects of China Petroleum & Chemical Corporation (No. 20212930037)。
文摘Mixing two or more polymers to produce the“polymer alloy”is one of the most versatile and economical strategies for developing new polymeric materials.The compatibility between polymer components largely determines the comprehensive performance of polymer blend.More recently,a type of unique surface partitioned materials,Janus particles,has been proposed to act as a novel interfacial compatibilizer for polymer blends.Such Janus particles integrates the amphipathicity of diblock copolymer and interfacial stabilization of nanoparticles,displaying a significant superiority in comparison with molecular compatibilizers for a wide range of polymer blends.In this review,we mainly focus on the compatibilizing effects of Janus nanofillers of various morphologies,including spherical,snowman-like,and two-dimensional nanosheets,on polymer blends.We shed light on the impacts of compatibilization of Janus particles on phase morphologies,mechanical properties,and functionalities of polymer blends.This review could provide a guidance for designing an effective Janus particle compatibilizer to develop high-performance polymer blends.
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the National Natural Science Foundation of China (No. 51633003) for the financial support
文摘Polyamide/acrylonitrile-butadiene-styrene copolymer(PA/ABS) blends have drawn considerable attention from both academia and industry for their important applications in automotive and electronic areas. Due to poor miscibility of PA and ABS, developing an effective compatibilization strategy has been an urgent challenge to achieve prominent mechanical properties. In this study, we create a set of mechanically enhanced PA6/ABS blends using two multi-monomer melt-grafted compatibilizers, SEBSg-(MAH-co-St) and ABS-g-(MAH-co-St). The dispersed domain size is significantly decreased and meanwhile the unique "soft shell-encapsulating-hard core" structures form in the presence of compatibilizers. The optimum mechanical performances manifest an increase of 36% in tensile strength and an increase of 1300% in impact strength, compared with the neat PA6/ABS binary blend.
基金financially supported by the National Natural Science Foundation of China(No.21304047)Natural Science Foundation of Jiangsu Province(No.13KJB430017)+1 种基金Research Fund for the Doctoral Program of Higher Education(No.20133221120015)Synergetic Innovation Center for Organic Electronics and Information Displays
文摘Donor-acceptor(D-A) type fully conjugated block copolymer systems have been rarely reported due to the challenges in synthetic approaches to prepare well-defined low-polydispersity products. In this work, fully conjugated block copolymers are synthesized in a one-pot reaction through Stille coupling polycondensation, by utilizing the end-functional polymer copolymerization method. End-functional P3HT are copolymerized with AA(2,7-dibromo-9-(heptadecan-9-yl)-9Hcarbazole) and BB(4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole, TBT) type monomers, respectively. The orthogonal solubility between the very soluble P3HT donor and the insoluble PCDTBT acceptor block improves the purity of block copolymers as well as distinct nano-scale phase-separation compared with other reports on miscibility of donor and acceptor polymer block. Further purification via preparative GPC is carried out to remove the excess of unreacted P3HT and free PCDTBT as well as to achieve low polydispersity of block copolymers. The chemical structure of the P3HTb-PCDTBT block copolymers are verified via ~1H-NMR, and further confirmed by FTIR spectra. The block copolymer shows broad absorption and moderate optical band gap of 1.8 e V. Furthermore, the fully conjugated block copolymer films exhibit significant fine structures, much smoother film morphology compared to P3HT/PCDTBT polymer blends. By adding a small amount of block copolymer P3HT-b-PCDTBT as a compatibilizer into the bulk-heterojunction of P3HT:PC_(61)BM blends, polymer solar cells with an 8% increase of short circuit current(J_(sc)) and 10% increase of power conversion efficiency(PCE) are achieved owing to the improvement of the active-layer film morphology. To the best of our knowledge, this is the first report on donor-acceptor type fully conjugated block copolymer as an effective ternary additive in polymer: fullerene bulk heterojunction solar cells.
基金the National Natural Science Foundation of China(No.21574097).
文摘In this work,the formation of cocontinuous structure in immiscible high density polyethylene/isotactic polypropylene(HDPE/iPP)blends was investigated for various olefin-based compatibilizers of distinct molecular architectures,including ternary random copolymer EPDM,olefin block copolymer(OBC),polypropylene-based OBC(PP-OBC),ethylene/a-olefin copolymer(POE),bottlebrush polymer poly(1-dodecene),and comb-like poly(propylene-co-high a-olefin)(PPO).The scanning electron microscopy results show that after adding OBC,PP-OBC,and POE copolymers,the finer droplet-in-matrix morphologies were obtained in 70/30 HDPE/iPP blend.Interestingly,for 70/30 HDPE/iPP blend with just 5 wt%of PPO copolymers,the phase inversion from droplet-in-matrix to cocontinuous morphology can be observed.It was proposed that the development of cocontinuous morphology contained the following steps:(1)in terfacial saturati on of compatibilizers and droplet deformation,(2)droplet-droplet coalesce nee,(3)continuity development,and(4)the formation of dual-phase con tinuity.Among the diverse copolymers studied in this work,PPO copolymer can be easily removed out of the interface during droplet coalescence and stabilize the curvature of minor fiber phase,facilitating the formation of cocontinuous morphology.In contrast,other olefin-based compatibilizers(EPDM,OBC,PP-OBC,and POE)exhibit the distinct steric repulsion effect to prohibit droplet coalescence.Moreover,the cocontinous interval varies with the compatibilizer architectures.Surprisingly,after adding 10 wt%of PPO copolymers,the cocontinuous interval was greatly broadened from HDPE/iPP range of 45/55-60/40 to that of 40/60-70/30.
基金This work was financially supported by the National Natural Science Foundation of China(No.51803224).
文摘The objective of this study was to improve the toughness of bio based brittle poly(ethylene 2,5-furandicarboxylate)(PEF)by melt blending with bio based polyamide11(PA11)in the presence of a reactive multifunctional epoxy compatibilizer(Joncryl ADR-4368).The morphological,thermal,rheological,and mechanical properties of PEF/PA11 blends were investigated.Compared with neat PEF,the toughness of PEF/PA11 blend was not improved in the absence of the reactive compatibilizer due to the poor compatibility between the two polymers.When Joncryl was incorporated into PEF/PA11 blends,the interfacial tension between PEF and PA11 was obviously reduced,reflecting in the fine average particle size and narrow distribution of PA11 dispersed phase as observed by scanning electron microscopy(SEM).The complex viscosities of PEF/PA11 blends with Joncryl were much higher than that of PEF/PA11 blend,which could be ascribed to the formation of graft copolymers through the epoxy groups of Joncryl reacting with the end groups of PEF and PA11 molecular chains.Thus,the compatibility and interfacial adhesion between PEF and PA11 were greatly improved in the presence of Joncryl.The compatibilized PEF/PA11 blend with 1.5 phr Joncryl exhibited significantly improved elongation at break and unnotch impact strength with values of 90.1%and 30.3kJ/m2,respectively,compared with those of 3.6%and 3.8 kJ/m2 for neat PEF,respectively.This work provides an effective approach to improve the toughness of PEF which may expand its widespread application in packaging.
基金supported by Science and Technology Support Plan of Suqian(H201510)the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)Nanjing Wurui Biodegradable Materials Research Institute.
文摘Poly(butylene adipate-co-terephthalate)(PBAT)and poly(butylene succinate-co-adipate)(PBSA)blend films were prepared with different contents of a multifunctional epoxide chain extender Joncryl ADR-4468(ADR)or benzoyl peroxide(BPO).The long-chain-branching(LCB)introduced by ADR and branched/crosslinked entanglement induced by BPO increased melt elasticity,viscosity and compatibility,as indicated by thermal properties,rheological and morphological analyses.It was found that the elongation at break and the tensile strength were significantly improved,due to the enhancement of compatibility and the interfacial adhesion by the incorporation of ADR or BPO.The best mechanical properties were obtained in PBAT/PBSA/ADR(60/40/0.3)(A4T6A_(0.3))and PBAT/PBSA/BPO(60/40/0.9)(A4T6B_(0.9))films,respectively.With the rapid initiation of chain growth by BPO,it has significantly improved the transparency of the film.ADR and BPO can be used interchangeably in improving the comprehensive properties of PBAT/PBSA films,and it would provide more strategies for developing biodegradable materials for various applications.
文摘Blend of natural rubber (NR) and chlorosulfonated polyethylene (CSM) was so interesting due to binding of the good oil resistance of CSM, the good mechanical properties and low cost of NR. However, due to the different polarities of two rubbers, phase separation and inferior properties of NR/CSM blend were obtained. The practical way to improve its properties is the addition of the third component to bind both phases of the blend. Effects of poly(vinyl chloride), PVC as compatibilizer on cure characteristics, morphology, mechanical properties and automotive fuel resistance of NR/ CSM blend were investigated. In this contribution, NR/CSM blend with blend ratio of 50/50 was prepared using a two-roll mill, and then vulcanized in a compression mold at 160°C. The PVC content was varied from 1 to 7 phr. It was found that the usage of 7 phr PVC led to improve interaction between NR and CSM phases. Therefore, increase in cure characteristics, mechanical strength and automotive fuel resistance of the blend was observed.
文摘The mechanical properties of composites prepared from wood flour and thermoplastic blends were investigated. Thermoplastic mixtures of polypropylene (PP) and high-density polyethylene (HDPE) and polystyrene (PS), virgin or recycled, were mixed with wood flour in a high speed blender and then extruded by a specially designed twin/single screw extruder system to form wood-flour/thermoplastic-blends composites (WTBCs). Comparative studies were made to evaluate the effectiveness of the two modification methods of the thermoplastic blends, the one of the addition of maleic anhydride grafted styrene-ethylene-butylene-styrene block copolymer (SEBS-g-MAH) as compatibilizer and the other of blend grafting of maleic anhydride (MAH) using dicumyl peroxide (DCP) as initiator by reactive extrusion. The results showed that the impact properties of WTBCs using SEBS-g-MAH as compatilizer were better improved than that of the blend grafting. However, adverse results were observed on the tensile and flexural properties of the corresponding WTBCs. The mechanical properties of WTBCs prepared from recycled plastic blends were poorer to some extent than that from virgin plastic blends in general, especially in elongation break. The morphology of WTBCs breaking section was analyzed by scanning electron microscopy (SEM) and the results showed that a good interfacial adhesion between wood flour and polymer matrix was observed with both of the two modification methods. However, by blend grafting of adding DCP as initiator and MAH as monomer, a better interfacial bonding between wood and plastic matrix was obtained than that of the addition of SEBS-g-MAH. Blend grafting can be considered as a potential way of increasing the interfacial compatibility of different plastics and between plastic blends and wood.
文摘An amphiphilic graft polymer, (PAM-g-PBA), polyacrylamide (PAM) having poly(n-butyl acrylate) (PBA) side chains, was obtained by radical copolymerization of acrylamide with PBA macromer in solution. The macromer was synthesized by free radical polymerization of butyl acrylate in the presence of different amounts of thioglycolic acid as the chain transfer agent, followed by termination with glycidyl methacrylate. The reactivity ratio and effects of copolymerization conditions on the conversion of macromer or grafting efficiency were studied. The crude products were purified by extraction with toluene and water successively. The purified graft copolymer was characterized by IR, DSC and TEM. PAM-g-PBA can bring about microphase separation and exhibits good emulsifying properties and water absorbency. PAM-g-PBA exhibits a very good compatibilizing effect on the acrylic rubber/poly(vinyl chloride) blends. 2%-3% of the graft copolymer is enough for enhancing the tensile strength of the blends. The tensile strength of the blends is more than twice that without the compatibilizer. DSC and SEM demonstrated the enhancement of compatibility in the presence of the graft copolymer.
基金Natural Science Foundation of Shanxi Province(No.20041010)
文摘The alloy of Nylon 6/acrylonitrile-butadiene-styrene(ABS)was used for a compatibilizer to generate the maleic anhydride(ABS-g-MAH),in which the proportion of PA6/ABS is 90/10.The results of the mechanical tests show that when the content of ABS-g-MAH is 20%,the impact strength of the alloy with the compatibilizer increased by around 41%,compared with that of the PA6/ABS alloy;Besides,the tensile strength has been significantly improved.Furthermore,in accordance with the dynamic mechanical analysis,α relaxation temperature of Nylon 6 has raised from 70 ℃ to 110 ℃ with the addition of ABS and ABS-g-MAH;moreover,and the obvious relaxations of β and γ occur at about 60 ℃ and-60 ℃,respectively.It can be seen from the scanning electron microscope(SEM)photographs that the compatibility has been improved through the addition of ABS-g-MAH.The water absorption of Nylon 6 has also been improved by the addition of ABS and ABS-g-MAH.When the content of ABS-g-MAH is 10%,the water absorption of the alloy will fall by 50%.
