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
To enhance the impact strength of polyamide 6, hydrolytic polymerization modification by the polyaminoamide-g-poly(ethylene glycol) (PAAEG) derivatives with poly(ethylene glycol) (PEG) molecular weight of 400-10000 wa...To enhance the impact strength of polyamide 6, hydrolytic polymerization modification by the polyaminoamide-g-poly(ethylene glycol) (PAAEG) derivatives with poly(ethylene glycol) (PEG) molecular weight of 400-10000 was studied. Amide groups of polyaminoamide segments were postulated to form hydrogen bonding with polyamide 6, and hydroxy groups of PAAEG units were expected to react with carboxylic acid groups of polyamide 6 forming copolymers during the polymerization. The improved compatibility in amorphous regions of blends has been confirmed by differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) of fracture surfaces. The effects of PAAEG on the water absorption and notch sensitivity of blends were investigated, using water uptake measurement and mechanical testings, respectively. For comparison, pure polyamide 6 and the blend of PEG/polyamide 6 were also investigated. The addition of PAAEG retarded the crystallization of polyamide 6, but did not make remarkable influences on its crystalline structure. As a consequence of the strong interactions between the dispersed phases and polyamide 6 matrices, PAAEG was a more suitable additive for improving the notched impact strength of polyamide 6 than PEG.展开更多
Polyamide （PA6） and polycarbonate （PC） were prepared by a Brabender mixer （ PLV- 151） at 240℃ with 30 rpm for duration of 8 and 6 minutes respectively. The epoxy resin （E） addition can lead to substantial mic...Polyamide （PA6） and polycarbonate （PC） were prepared by a Brabender mixer （ PLV- 151） at 240℃ with 30 rpm for duration of 8 and 6 minutes respectively. The epoxy resin （E） addition can lead to substantial microstructural changes in the PA6/PC blends. Scanning electron microscope （SEM） was used to observe the mixtures characterized by the domains of clearly segregated homophases and voids between the two polymers. PA6/PC of polyamide 6 and polycarbonate with epoxy resin addition under the composition ratio of 20/80, 20/80/1, 40/60/1 and 40/60, were tested to verify the key role of epoxy in promoting the compatibility of PA6 with PC during blending.展开更多
The effect of blending routes on the morphology and properties of Polyamide-6 (PA-6)/nano-CaCO3/Maleated ethylene-octane copolymer (MA-POE) ternary composite was analyzed using static mechanical test (DMA), TEM (trans...The effect of blending routes on the morphology and properties of Polyamide-6 (PA-6)/nano-CaCO3/Maleated ethylene-octane copolymer (MA-POE) ternary composite was analyzed using static mechanical test (DMA), TEM (transmission electronic microscope) and SEM (scanning electron microscope). It was found that MA-POE, as an impact modifier, had a profound effect upon the toughness of the PA-6/nano-CaCO3 composite. In particular, by adopting two-stage blending route, the microstructure of the ternary composites turned to core-shell structure, and the impact toughness was improved greatly. At the same time, tensile strength and dynamic storage modulus (E1) were higher than those with one-stage blending route processed ternary composite. The results suggest that blending routes may improve the properties of PA-6/nano-CaCO3/MA-POE ternary composites.展开更多
用多组分熔融接枝的方法将甲基丙烯酸缩水甘油酯 (GMA)和苯乙烯 (St)共同接枝到聚丙烯 (PP)上 ,制得具有较高GMA接枝率的多单体接枝聚丙烯 ,PP g (GMA co St) .将PP g (GMA co St)与尼龙 6 (PA6 )进行共混 ,利用扫描电镜 (SEM) ,差示扫...用多组分熔融接枝的方法将甲基丙烯酸缩水甘油酯 (GMA)和苯乙烯 (St)共同接枝到聚丙烯 (PP)上 ,制得具有较高GMA接枝率的多单体接枝聚丙烯 ,PP g (GMA co St) .将PP g (GMA co St)与尼龙 6 (PA6 )进行共混 ,利用扫描电镜 (SEM) ,差示扫描量热计 (DSC)和广角X射线衍射 (WAXD)对共混物的形态和结晶进行了研究 .在共混过程中 ,PP g (GMA co St)与PA6反应原位生成了PP g PA6 ,有效改善了共混物的相容性 ,分散相尺寸明显减小 .在PP g (GMA co St) PA6为 3 7的体系中 ,PP g (GMA co St)出现分级结晶现象 ,其在较低温度下的结晶属于均相成核结晶 .在PP g (GMA co St) PA6为 7 3的体系中 ,由于PA6相分散细微 ,在通常结晶温度下不结晶 ,而是在低温下均相成核与PP g (GMA co St)同时结晶 .WAXD证实体系中接枝PP ,PA6为分别结晶 。展开更多
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.
基金supported by the National Natural Science Foundation of China(No.20707008)China Petroleum & Chemical Corporation.
文摘To enhance the impact strength of polyamide 6, hydrolytic polymerization modification by the polyaminoamide-g-poly(ethylene glycol) (PAAEG) derivatives with poly(ethylene glycol) (PEG) molecular weight of 400-10000 was studied. Amide groups of polyaminoamide segments were postulated to form hydrogen bonding with polyamide 6, and hydroxy groups of PAAEG units were expected to react with carboxylic acid groups of polyamide 6 forming copolymers during the polymerization. The improved compatibility in amorphous regions of blends has been confirmed by differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) of fracture surfaces. The effects of PAAEG on the water absorption and notch sensitivity of blends were investigated, using water uptake measurement and mechanical testings, respectively. For comparison, pure polyamide 6 and the blend of PEG/polyamide 6 were also investigated. The addition of PAAEG retarded the crystallization of polyamide 6, but did not make remarkable influences on its crystalline structure. As a consequence of the strong interactions between the dispersed phases and polyamide 6 matrices, PAAEG was a more suitable additive for improving the notched impact strength of polyamide 6 than PEG.
文摘Polyamide （PA6） and polycarbonate （PC） were prepared by a Brabender mixer （ PLV- 151） at 240℃ with 30 rpm for duration of 8 and 6 minutes respectively. The epoxy resin （E） addition can lead to substantial microstructural changes in the PA6/PC blends. Scanning electron microscope （SEM） was used to observe the mixtures characterized by the domains of clearly segregated homophases and voids between the two polymers. PA6/PC of polyamide 6 and polycarbonate with epoxy resin addition under the composition ratio of 20/80, 20/80/1, 40/60/1 and 40/60, were tested to verify the key role of epoxy in promoting the compatibility of PA6 with PC during blending.
基金This work was financially supported by the National Natural Science Foundation of China under grant No.29934070.
文摘The effect of blending routes on the morphology and properties of Polyamide-6 (PA-6)/nano-CaCO3/Maleated ethylene-octane copolymer (MA-POE) ternary composite was analyzed using static mechanical test (DMA), TEM (transmission electronic microscope) and SEM (scanning electron microscope). It was found that MA-POE, as an impact modifier, had a profound effect upon the toughness of the PA-6/nano-CaCO3 composite. In particular, by adopting two-stage blending route, the microstructure of the ternary composites turned to core-shell structure, and the impact toughness was improved greatly. At the same time, tensile strength and dynamic storage modulus (E1) were higher than those with one-stage blending route processed ternary composite. The results suggest that blending routes may improve the properties of PA-6/nano-CaCO3/MA-POE ternary composites.
文摘用多组分熔融接枝的方法将甲基丙烯酸缩水甘油酯 (GMA)和苯乙烯 (St)共同接枝到聚丙烯 (PP)上 ,制得具有较高GMA接枝率的多单体接枝聚丙烯 ,PP g (GMA co St) .将PP g (GMA co St)与尼龙 6 (PA6 )进行共混 ,利用扫描电镜 (SEM) ,差示扫描量热计 (DSC)和广角X射线衍射 (WAXD)对共混物的形态和结晶进行了研究 .在共混过程中 ,PP g (GMA co St)与PA6反应原位生成了PP g PA6 ,有效改善了共混物的相容性 ,分散相尺寸明显减小 .在PP g (GMA co St) PA6为 3 7的体系中 ,PP g (GMA co St)出现分级结晶现象 ,其在较低温度下的结晶属于均相成核结晶 .在PP g (GMA co St) PA6为 7 3的体系中 ,由于PA6相分散细微 ,在通常结晶温度下不结晶 ,而是在低温下均相成核与PP g (GMA co St)同时结晶 .WAXD证实体系中接枝PP ,PA6为分别结晶 。
