A novel polypropylene random(PPR)composite materials with optimized properties was developed by addingβ-nucleating compound agents(rare earth complex WBG-2 and aryl amide derivative TMB-5)and ternary compound modifie...A novel polypropylene random(PPR)composite materials with optimized properties was developed by addingβ-nucleating compound agents(rare earth complex WBG-2 and aryl amide derivative TMB-5)and ternary compound modifier(TPE/WBG-2/CaCO_(3)).The effects of differentβ-nucleating agents and ternary compound modifier on the mechanical properties and crystallization behavior of PPR were analyzed.The results show that,compared with pure PPR materials,both WBG-2 and TMB-5 could significantly improve the impact strength of PPR.The crystallization temperature of PPR increased with the addition ofβ-nucleating agent.The modified PPR prepared with ternary compound modifier showed the most excellent comprehensive properties.展开更多
Biodegradable poly(epsilon-caprolactone-co-p-dioxanone)(PCDO) random copolymers have been synthesized by ring-opening polymerization of epsilon-caprolactone(CL) and p-dioxanone(PDO) under microwave irradiation.The eff...Biodegradable poly(epsilon-caprolactone-co-p-dioxanone)(PCDO) random copolymers have been synthesized by ring-opening polymerization of epsilon-caprolactone(CL) and p-dioxanone(PDO) under microwave irradiation.The effects of irradiation time and different CL/PDO molar feed ratios on the microwave-assisted ring-opening polymerization(MROP) of PCDO have been discussed.The resultant products were characterized by ~1H NMR,GPC and DSC.It was found that the polymerization was completed within 20 min at 140℃.In th...展开更多
A Monte Carlo method was used to take thorough account of the influences of different reactivity ratios and initial feed compositions on copolymer microstructure.The model proves the lack of azeotropic behavior in sys...A Monte Carlo method was used to take thorough account of the influences of different reactivity ratios and initial feed compositions on copolymer microstructure.The model proves the lack of azeotropic behavior in systems in which r_A>1 and r_B<1 or vice versa;it is also able to calculate the drift in the copolymer properties:copolymer composition,and randomness parameter.Moreover,for each reactivity ratio pair given,there is a unique reaction conversion,at which macromolecules produced inherit their ...展开更多
A series of random and block poly（ L-lactide-co-e-caprolactone ） （ PCLA ） copolymers whh different composition are prepared using stannous octaoate as catalyst.The effects of the amount of initiator on the intrins...A series of random and block poly（ L-lactide-co-e-caprolactone ） （ PCLA ） copolymers whh different composition are prepared using stannous octaoate as catalyst.The effects of the amount of initiator on the intrinsic viscosity have been investigated. The structure of the PCLA copolymers is characterized by means of nuclear magnetic resonance（ NMR ）, Fourier transform infrared spectrum （ FTIR ）, differential scanning calorimetry （ DSC ） and X- ray diffraction （ XRD ） methods. It is shown that the synthesis condition and the composition of copolymers obrious influence on the structure of PCLA copolymers. Hydrolytic degradation of the copolymers in a PBS solution of pH 7.4 at 37.0℃ shows that the copolymers of different composhions degrade at different rates.展开更多
采用差示扫描量热仪、广角X射线衍射仪、扫描电子显微镜,从微观角度探讨退火对无规共聚聚丙烯(Polypropylene Random Copolymer,PPR)管材结晶行为和抗低温冲击性能的影响。结果表明,退火能够有效地提高PPR管材低温下抗冲击性能,在-18℃...采用差示扫描量热仪、广角X射线衍射仪、扫描电子显微镜,从微观角度探讨退火对无规共聚聚丙烯(Polypropylene Random Copolymer,PPR)管材结晶行为和抗低温冲击性能的影响。结果表明,退火能够有效地提高PPR管材低温下抗冲击性能,在-18℃环境下进行落锤冲击实验,退火后PPR管材的破损比由90%减少至50%。退火不仅可以促进PPR管材内分子链重新排列、提高其规整性、消除PPR管材的热应力,还可以提高PPR管材的结晶度、诱导内部β晶的生成,从而提高其抗冲击韧性。展开更多
Antimicrobial peptides(AMPs)have been considered as an alternative to small molecule antibiotics since they are difficult to develop antimicrobial resistance.Hyperbranched polylysine(HPL),an AMP mimics,has gained atte...Antimicrobial peptides(AMPs)have been considered as an alternative to small molecule antibiotics since they are difficult to develop antimicrobial resistance.Hyperbranched polylysine(HPL),an AMP mimics,has gained attention due to its broad-spectrum antibacterial activities,but it also suffers from high toxicity.Here we report a facile strategy to engineer the toxicity of HPL by copolymerizing lysine(K)with a hydrophobic amino acid,e.g.,alanine(A),tryptophan(W)or phenylalanine(F),to afford hyperbranched random copolymers.These copolymers have comparable antibacterial activities to HPL while their cytotoxicities and in vivo toxicities are lowered when the type and content of hydrophobic amino acid and the size of copolymers are optimized.The G.mellonella infection model demonstrates that the copolymers are effective against the S.aureus infection in vivo.The copolymers kill the bacteria through the disruption of cell membranes and the bacteria do not develop resistance to the copolymers.展开更多
The design of crosslinking domains is a vital factor to create functional hydrogels with controlled physical,mechanical,and adhesive properties.This paper demonstrates versatile synthetic systems of micelle-crosslinke...The design of crosslinking domains is a vital factor to create functional hydrogels with controlled physical,mechanical,and adhesive properties.This paper demonstrates versatile synthetic systems of micelle-crosslinked hydrogels with highly stretchable,self-healing,and selectively adhesive properties.For this,methacrylate-bearing random copolymer micelles are designed as physical and covalent crosslink domains via the self-assembly of amphiphilic random copolymers carrying hydrophilic poly(ethylene glycol)(PEG),hydrophobic butyl or dodecyl groups,and methacrylate-terminal PEG in water.The size,aggregation number,and pendant methacrylate number of the micelles are controlled by the composition and degree of polymerization.Hydrogels are efficiently obtained from the free radical polymerization of hydrophilic monomers such as PEG acrylate and acrylamide in the presence of the micelle crosslinkers in water.Owing to the dynamic yet selective chain exchange properties of the micelle domains,the hydrogels are highly stretchable up to over 1000%and show self-healing and selectively adhesive properties.The self-healing of hydrogels is promoted upon heating due to the fast chain exchange of the micelle domains,whereas hydrogels consisting of micelles with different alkyl groups are never adhesive because of their self-sorting properties.展开更多
Starting from an initial sample of butene-1/ethylene copolymer with stable form I＇, we examined the nucleation of different crystalline polymorphs （here metastable form II and stable form I＇） at different isother...Starting from an initial sample of butene-1/ethylene copolymer with stable form I＇, we examined the nucleation of different crystalline polymorphs （here metastable form II and stable form I＇） at different isothermal crystallization temperatures after being melted at different melt temperature （Tmelt）. When Tmelt was just above the melting temperature （Tm） of the crystallites, self-seeding took place. There, residue crystallites served as nuclei leading to the crystallization of the same crystalline phase. When Tmelt was a few degrees above the Tin, self-seeding was disabled due to complete melting of the initial crystals. Upon crystallization, the selection of the different polymorphs in this random copolymer was found to depend on an interplay between the domain size of segregated long crystallizable sequences and the size and energy barrier of the critical nucleus of the respective crystalline forms. Our results provide a clear understanding of the polymorphs selection during crystallization of a random copolymer as well as homo-polymers under confinement.展开更多
Long chain branched polypropylene random copolymers （LCB-PPRs） were prepared via reactive extrusion with the addition of dicumyl peroxide （DCP） and various amounts of 1,6-hexanediol diacrylate （HDDA） into PPR. F...Long chain branched polypropylene random copolymers （LCB-PPRs） were prepared via reactive extrusion with the addition of dicumyl peroxide （DCP） and various amounts of 1,6-hexanediol diacrylate （HDDA） into PPR. Fourier transform infrared spectrometer （FTIR） was applied to confirm the existence of branching and（ investigate the grafting degree for the modified PPRs. Melt flow index （MFI） and oscillatory shear rheological properties including complex viscosity, storage modulus, loss tangent and the Cole-Cole plots were studied to differentiate the LCB-PPRs from linear PPR. Differential scanning calorimetry （DSC） and polarized light microscopy （PLM） were used to study the melting and crystallization behavior and the spherulite morphology, respectively. Qualitative and quantitative analyses of rheological curves demonstrated the existence of LCB. The effect of the LCB on crystalline morphology, crystallization behavior and molecular mobility, and, thereby, the mechanical properties were studied and analyzed. Due to the entanglements between molecular chains and the nucleating effect of LCB, LCB-PPRs showed higher crystallization temperature and crystallinity, higher crystallization rate, more uniformly dispersed and much smaller crystallite compared with virgin PPR, thus giving rise to significantly improve impact strength. Moreover, the LCB-PPRs exhibited the improved yield strength. The mobility of the molecular chain segments, as demonstrated by dynamic mechanical analysis （DMA）, was improved for the modified PPRs, which also contributed to the improvement of their mechanical properties.展开更多
Although addition of β-nucleating agent directly into homo-polypropylene （PPH） is a useful method to improve ,β-crystal content and toughen PPH, polypropylene random copolymer （PPR） makes this method powerless d...Although addition of β-nucleating agent directly into homo-polypropylene （PPH） is a useful method to improve ,β-crystal content and toughen PPH, polypropylene random copolymer （PPR） makes this method powerless due to its random structure and low crystallinity. In this study, the β-nucleated PPR with high β-crystal content was prepared by a novel high effective β-nucleating system which consists of β-nucleation agent （TMB-5） and modified zeolite 13X （M13X）. It was found that M13X and TMB-5 had a synergistic influence on improving β-crystal content and toughening PPR. The content of β-crystal in PPR/M13X/TMB-5 was significantly larger than the sum of that in PPR/M13X and PPR/TMB-5. Besides, fracture behavior, phase morphology and relaxation of matrix chain segments were also investigated. The results showed that M13X and TMB-5 improved the mobility of amorphous chain segments at low temperature and contributed to much energy dissipation. This work provides a powerful method to modify PPR.展开更多
Copolymers of 1,3-butadiene and p-methylstyrene （p-MS） were synthesized via anionic polymerization. A benzophenone-potassium complex was added to tune the reactivity ratio of the two monomers, leading to random and ...Copolymers of 1,3-butadiene and p-methylstyrene （p-MS） were synthesized via anionic polymerization. A benzophenone-potassium complex was added to tune the reactivity ratio of the two monomers, leading to random and gradient composition alonglthe copolymer chain. The overall composition and microstructure could be controlled and well characterized by GPC and H-NMR. The p-MS was distributed from gradient to random with increasing the content of the benzophenone-potassium complex, and the 1,2-microstrucmre in the polybutadiene sequence increased at the same time. The hydrogenation of the copolymer of 1,3-butadiene and p-MS resulted in the corresponding saturated copolymer with well- defined structure and narrow molecular weight distribution.展开更多
The binary random in-chain silyl-hydride multi-functionalized poly（styrene/butadiene/isoprene and dimethyl[4-（1-phenylvinyl） phenyl]silane） （PS-DPESiH, PB-DPESiH, PI-DPESiH） copolymers were successfully synthesi...The binary random in-chain silyl-hydride multi-functionalized poly（styrene/butadiene/isoprene and dimethyl[4-（1-phenylvinyl） phenyl]silane） （PS-DPESiH, PB-DPESiH, PI-DPESiH） copolymers were successfully synthesized. These functionalized copo- lymers were prepared in hexane with n-BuLi as the initiator at 50℃ for 4 h. The silyl-hydride groups were introduced into polymer backbones quantitatively by living anionic polymerization. The copolymers were determined through 1H NMR, size exclusion chromatography （SEC） and differential scanning calorimetry （DSC） techniques, while the number of silyl-hych-ide groups was calculated and discussed.展开更多
基金Funded by the Natural Science Foundation of Liaoning Province of China(No.20180550432)Natural Science Foundation for Young Doctoral Research(No.2020-BS-158)Basic Scientific Research Project of Colleges and Universities of Liaoning Provincial Department of Education(No.LJKQZ2021060)。
文摘A novel polypropylene random(PPR)composite materials with optimized properties was developed by addingβ-nucleating compound agents(rare earth complex WBG-2 and aryl amide derivative TMB-5)and ternary compound modifier(TPE/WBG-2/CaCO_(3)).The effects of differentβ-nucleating agents and ternary compound modifier on the mechanical properties and crystallization behavior of PPR were analyzed.The results show that,compared with pure PPR materials,both WBG-2 and TMB-5 could significantly improve the impact strength of PPR.The crystallization temperature of PPR increased with the addition ofβ-nucleating agent.The modified PPR prepared with ternary compound modifier showed the most excellent comprehensive properties.
文摘Biodegradable poly(epsilon-caprolactone-co-p-dioxanone)(PCDO) random copolymers have been synthesized by ring-opening polymerization of epsilon-caprolactone(CL) and p-dioxanone(PDO) under microwave irradiation.The effects of irradiation time and different CL/PDO molar feed ratios on the microwave-assisted ring-opening polymerization(MROP) of PCDO have been discussed.The resultant products were characterized by ~1H NMR,GPC and DSC.It was found that the polymerization was completed within 20 min at 140℃.In th...
文摘A Monte Carlo method was used to take thorough account of the influences of different reactivity ratios and initial feed compositions on copolymer microstructure.The model proves the lack of azeotropic behavior in systems in which r_A>1 and r_B<1 or vice versa;it is also able to calculate the drift in the copolymer properties:copolymer composition,and randomness parameter.Moreover,for each reactivity ratio pair given,there is a unique reaction conversion,at which macromolecules produced inherit their ...
文摘A series of random and block poly（ L-lactide-co-e-caprolactone ） （ PCLA ） copolymers whh different composition are prepared using stannous octaoate as catalyst.The effects of the amount of initiator on the intrinsic viscosity have been investigated. The structure of the PCLA copolymers is characterized by means of nuclear magnetic resonance（ NMR ）, Fourier transform infrared spectrum （ FTIR ）, differential scanning calorimetry （ DSC ） and X- ray diffraction （ XRD ） methods. It is shown that the synthesis condition and the composition of copolymers obrious influence on the structure of PCLA copolymers. Hydrolytic degradation of the copolymers in a PBS solution of pH 7.4 at 37.0℃ shows that the copolymers of different composhions degrade at different rates.
文摘采用差示扫描量热仪、广角X射线衍射仪、扫描电子显微镜,从微观角度探讨退火对无规共聚聚丙烯(Polypropylene Random Copolymer,PPR)管材结晶行为和抗低温冲击性能的影响。结果表明,退火能够有效地提高PPR管材低温下抗冲击性能,在-18℃环境下进行落锤冲击实验,退火后PPR管材的破损比由90%减少至50%。退火不仅可以促进PPR管材内分子链重新排列、提高其规整性、消除PPR管材的热应力,还可以提高PPR管材的结晶度、诱导内部β晶的生成,从而提高其抗冲击韧性。
基金financially supported by the National Natural Science Foundation of China(No.51973212)Department of Science and Technology of Jilin Province(Nos.20210203119SF and 20210203173SF)。
文摘Antimicrobial peptides(AMPs)have been considered as an alternative to small molecule antibiotics since they are difficult to develop antimicrobial resistance.Hyperbranched polylysine(HPL),an AMP mimics,has gained attention due to its broad-spectrum antibacterial activities,but it also suffers from high toxicity.Here we report a facile strategy to engineer the toxicity of HPL by copolymerizing lysine(K)with a hydrophobic amino acid,e.g.,alanine(A),tryptophan(W)or phenylalanine(F),to afford hyperbranched random copolymers.These copolymers have comparable antibacterial activities to HPL while their cytotoxicities and in vivo toxicities are lowered when the type and content of hydrophobic amino acid and the size of copolymers are optimized.The G.mellonella infection model demonstrates that the copolymers are effective against the S.aureus infection in vivo.The copolymers kill the bacteria through the disruption of cell membranes and the bacteria do not develop resistance to the copolymers.
基金Japan Society for the Promotion of Science KAKENHI,Grant/Award Numbers:JP19K22218,JP20H02787,JP20H05219,JP22H04539The Ogasawara Foundation for the Promotion of Science&Engineering+1 种基金Noguchi InstituteIketani Science and Technology Foundation。
文摘The design of crosslinking domains is a vital factor to create functional hydrogels with controlled physical,mechanical,and adhesive properties.This paper demonstrates versatile synthetic systems of micelle-crosslinked hydrogels with highly stretchable,self-healing,and selectively adhesive properties.For this,methacrylate-bearing random copolymer micelles are designed as physical and covalent crosslink domains via the self-assembly of amphiphilic random copolymers carrying hydrophilic poly(ethylene glycol)(PEG),hydrophobic butyl or dodecyl groups,and methacrylate-terminal PEG in water.The size,aggregation number,and pendant methacrylate number of the micelles are controlled by the composition and degree of polymerization.Hydrogels are efficiently obtained from the free radical polymerization of hydrophilic monomers such as PEG acrylate and acrylamide in the presence of the micelle crosslinkers in water.Owing to the dynamic yet selective chain exchange properties of the micelle domains,the hydrogels are highly stretchable up to over 1000%and show self-healing and selectively adhesive properties.The self-healing of hydrogels is promoted upon heating due to the fast chain exchange of the micelle domains,whereas hydrogels consisting of micelles with different alkyl groups are never adhesive because of their self-sorting properties.
基金financially supported by the National Natural Science Foundation of China(Nos.21134006 and 51525305)
文摘Starting from an initial sample of butene-1/ethylene copolymer with stable form I＇, we examined the nucleation of different crystalline polymorphs （here metastable form II and stable form I＇） at different isothermal crystallization temperatures after being melted at different melt temperature （Tmelt）. When Tmelt was just above the melting temperature （Tm） of the crystallites, self-seeding took place. There, residue crystallites served as nuclei leading to the crystallization of the same crystalline phase. When Tmelt was a few degrees above the Tin, self-seeding was disabled due to complete melting of the initial crystals. Upon crystallization, the selection of the different polymorphs in this random copolymer was found to depend on an interplay between the domain size of segregated long crystallizable sequences and the size and energy barrier of the critical nucleus of the respective crystalline forms. Our results provide a clear understanding of the polymorphs selection during crystallization of a random copolymer as well as homo-polymers under confinement.
基金financially supported by the Foundation for Development of Science and Technology of Fuzhou University(No.2011-XY-1)
文摘Long chain branched polypropylene random copolymers （LCB-PPRs） were prepared via reactive extrusion with the addition of dicumyl peroxide （DCP） and various amounts of 1,6-hexanediol diacrylate （HDDA） into PPR. Fourier transform infrared spectrometer （FTIR） was applied to confirm the existence of branching and（ investigate the grafting degree for the modified PPRs. Melt flow index （MFI） and oscillatory shear rheological properties including complex viscosity, storage modulus, loss tangent and the Cole-Cole plots were studied to differentiate the LCB-PPRs from linear PPR. Differential scanning calorimetry （DSC） and polarized light microscopy （PLM） were used to study the melting and crystallization behavior and the spherulite morphology, respectively. Qualitative and quantitative analyses of rheological curves demonstrated the existence of LCB. The effect of the LCB on crystalline morphology, crystallization behavior and molecular mobility, and, thereby, the mechanical properties were studied and analyzed. Due to the entanglements between molecular chains and the nucleating effect of LCB, LCB-PPRs showed higher crystallization temperature and crystallinity, higher crystallization rate, more uniformly dispersed and much smaller crystallite compared with virgin PPR, thus giving rise to significantly improve impact strength. Moreover, the LCB-PPRs exhibited the improved yield strength. The mobility of the molecular chain segments, as demonstrated by dynamic mechanical analysis （DMA）, was improved for the modified PPRs, which also contributed to the improvement of their mechanical properties.
基金financially supported by the National Natural Science Foundation of China(No.50803042)Chengdu Economic & Technological Development Zone and Chuanlu Group
文摘Although addition of β-nucleating agent directly into homo-polypropylene （PPH） is a useful method to improve ,β-crystal content and toughen PPH, polypropylene random copolymer （PPR） makes this method powerless due to its random structure and low crystallinity. In this study, the β-nucleated PPR with high β-crystal content was prepared by a novel high effective β-nucleating system which consists of β-nucleation agent （TMB-5） and modified zeolite 13X （M13X）. It was found that M13X and TMB-5 had a synergistic influence on improving β-crystal content and toughening PPR. The content of β-crystal in PPR/M13X/TMB-5 was significantly larger than the sum of that in PPR/M13X and PPR/TMB-5. Besides, fracture behavior, phase morphology and relaxation of matrix chain segments were also investigated. The results showed that M13X and TMB-5 improved the mobility of amorphous chain segments at low temperature and contributed to much energy dissipation. This work provides a powerful method to modify PPR.
基金the National Natural Science Foundation of China(Nos.51073149 and 51233005)
文摘Copolymers of 1,3-butadiene and p-methylstyrene （p-MS） were synthesized via anionic polymerization. A benzophenone-potassium complex was added to tune the reactivity ratio of the two monomers, leading to random and gradient composition alonglthe copolymer chain. The overall composition and microstructure could be controlled and well characterized by GPC and H-NMR. The p-MS was distributed from gradient to random with increasing the content of the benzophenone-potassium complex, and the 1,2-microstrucmre in the polybutadiene sequence increased at the same time. The hydrogenation of the copolymer of 1,3-butadiene and p-MS resulted in the corresponding saturated copolymer with well- defined structure and narrow molecular weight distribution.
基金sponsored by the National Natural Science Foundation of China(Nos.21034001,21174021)
文摘The binary random in-chain silyl-hydride multi-functionalized poly（styrene/butadiene/isoprene and dimethyl[4-（1-phenylvinyl） phenyl]silane） （PS-DPESiH, PB-DPESiH, PI-DPESiH） copolymers were successfully synthesized. These functionalized copo- lymers were prepared in hexane with n-BuLi as the initiator at 50℃ for 4 h. The silyl-hydride groups were introduced into polymer backbones quantitatively by living anionic polymerization. The copolymers were determined through 1H NMR, size exclusion chromatography （SEC） and differential scanning calorimetry （DSC） techniques, while the number of silyl-hych-ide groups was calculated and discussed.
