Compatibilization and toughening of immiscible ternary blends of polyamide 1010, polypropylene, and ABS resin

2012 ◽  
Vol 32 (8-9) ◽  
pp. 487-492 ◽  
Author(s):  
Jiamin Zhang ◽  
Yongfang Li ◽  
Yong Zhu ◽  
Maojin Cui ◽  
Xiaoying Jiang

Abstract The ternary blends of three versatile polymers of polyamide 1010 (PA1010), polypropylene (PP), and ABS resin (ABS) were studied. As a compatibilizer, PP was multimonomer melt grafted in the presence of maleic anhydride (MAH), styrene (St), and dicumyl peroxide. The effects of multimonomers melt grafting blends of MAH and St on the crystallization behavior, morphology, and mechanical properties of PA1010/ABS/PP blends were investigated. The results showed that the graft copolymer generated in situ by the anhydride groups of grafted PP (g-PP) and the amino end of PA1010 has reduced the interfacial tension of blends efficiently. The interaction of St groups of the graft copolymer with ABS was helpful to improve the compatibility of the three components during melt blending process. The size of dispersed phases in the blends was reduced remarkably and the mechanical pro­perties were greatly improved when the content of g-PP in PA1010/ABS/PP blends is increased to 10%. The tensile strength of the compatibilized PA1010/ABS/PP blends was improved by a factor of 11.7, whereas the impact strength and elongation at break were increased by 4 and 4.9 times, respectively. The introduction of multimonomer melt g-PP is shown to be an effective approach to modifying immiscible multipolymer blends, which have many potential applications.

2011 ◽  
Vol 239-242 ◽  
pp. 3146-3149
Author(s):  
Jia Min Zhang ◽  
Ming Yi Zhu ◽  
Zhao Xun Lian

The impacts of multi-monomers melt grafting blends of maleic anhydride(MAH) and Styrene (St) on the crystallization behavior, morphology and mechanical properties of PA1010/ABS/PP blends were studied through the methods of SEM,themal analysis, mechanical properties analysis. The results showed that the graft copolymer generated in situ by the anhydride groups of g-PP and the amino end of PA1010 reduced the interfacial tension of blends efficiently, and the interaction of the styrene groups of the graft copolymer and ABS is helpful to improve the compatibility of three components during the melt blending process. The size of dispersed phase in blends is reduced obviously and the mechanical properties have a great improvement when the percentage of g-PP in the PA1010/ABS/PP blends increases to 10%. The tensile strength of the compatibilized PA1010/ABS/PP blends is improved by 11.7%,and the impact strength and elongation at break are increased 4 times and 4.9 times, respectively.


2011 ◽  
Vol 189-193 ◽  
pp. 533-536 ◽  
Author(s):  
Jia Min Zhang ◽  
Ming Yi Zhu ◽  
Zhao Xun Lian ◽  
Rong Zhu

With the melt grafting method using styrene (St) as co-monomer to maleic anhydride (MAH),the VERSIFY (V ethylene-propylene copolymer of the content of ethylene is 12%) was grafted. Different graft yield materials, V-g-(MAH-co-St) (g-V) were obtained. Nylon 6 (PA6)/ PP blends were prepared using twin-screw extruder. Using MFR, SEM, IR and mechanical properties testing analysis methods, morphology and mechanical properties of PA6/PP blends were studying on the different graft yield g-V. The results showed with increasing the graft yield, the minimum melt flow rate decreased and the size of the PP dispersed phase became smaller and more uniform. The addition of taller graft yield materials remarkably improved that the anhydride group in g-V reacted with the amine end groups of the PA6, and PP-PA6 copolymers were formed in situ, which effectively improved the compatibility between PP and PA6. The size of PP domains in the PA6 matrix was significantly reduced. Multi-monomer melt grafting can obtain a high rate of graft material. From the MAH: St = 0.5 to the MAH: St = 1, the grafting yield increased significantly. Continuing to improve MAH: St ratio, the magnitude of changes of graft yield of grafting decreases. Different grafting yield of multi-monomer g-V toughened PA6, a high rate of graft effect was good.


Materials ◽  
2019 ◽  
Vol 12 (2) ◽  
pp. 294 ◽  
Author(s):  
Mingfeng Xia ◽  
Wenchao Lang ◽  
Yue Yang ◽  
Jihang Yu ◽  
Ningjing Wu ◽  
...  

A series of different contents of glycidyl methacrylate (GMA)-grafted natural rubber (GNR) copolymers were fabricated via green bulk melt-grafting reactions, and super-tough bio-based poly (lactic acid) (PLA)/GNR thermoplastic vulcanizates (TPVs) were achieved by in-situ dynamic vulcanization. Increasing the graft yield, gel fraction, and crosslinking density of GNR vulcanizates effectively improved the ductility of the PLA/GNR TPVs, while prolonging the dynamic vulcanization time and increasing the GMA graft yield led to a notable enhancement in the impact toughness of the PLA/GNR TPVs. PLA/30 wt % GNR TPVs exhibited a significantly increased elongation (410%) and notched impact strength (73.2 kJ/m2), which were 40 and 15 times higher than those of the PLA/30 wt % NR TPVs, respectively. The new bio-based PLA/GNR TPVs offer promise as replacements for petroleum-based polymers in the automotive, 3D printing, and packaging fields.


2013 ◽  
Vol 634-638 ◽  
pp. 1836-1839
Author(s):  
Hong Kai Zhao ◽  
Li Guang Xiao ◽  
Jing Wu Gao

Macromolecule modification activator was prepared using prepolymer of HTBN end capped by HDI biuret (N-75). Then the ABS/PA6 co-blend polymer was prepared by anionic polymerization with putting ABS resin into molten caprolactam monomer at the temperature of 160°C~180°C and the sodium hydroxide being used as activator. In the system of in-situ synthetic ABS modified nylon resin ,when the content of ABS is at 10% with rubber modifier as compatiblizing agent for ABS and nylon, the impact strength of matrices stepped up obviously, and the effect is better than that in the system of rubber modification. Along with added ABS, the tensile strength and bending strength fell that is lower than the tensile strength of pure nylon but apparently higher than that of the rubber modification system. The increase usage of compatiblizing agent improved the intensity and rupture elongation of matrices. It was indicated that ABS obstructed spherulitic growth and resulted in the reduction of nylon crystallinity.


2005 ◽  
Vol 21 (4) ◽  
pp. 261-276 ◽  
Author(s):  
Sani Amril Samsudin ◽  
Azman Hassan ◽  
Munirah Mokhtar ◽  
Syed Mustafa Syed Jamaluddin

Blends of polystyrene (PS) with polypropylene (PP) are usually developed to overcome the inherent brittleness of PS. However, PS with PP are immiscible and (in the absence of a compatibiliser) incompatible. The present study investigated the effects of styrene-b (ethylene-co-butylene)-b-styrene (SEBS) on the mechanical properties and compatibility of PS-rich PS/PP blends. Using a Brabender PL2000 twin-screw extruder, blends of PS/PP in various compositions ranging from 100-60 wt% PS with and without SEBS were prepared and injection moulded. The overall results clearly showed that the mechanical properties of PS/PP blends are dependent on blend composition (ratio of PS/PP) and SEBS content. The impact strength and elongation at break of the PS/PP blends increase with SEBS content, at the expense of tensile strength and flexural modulus. The improvements in impact strength and elongation at break with the addition of SEBS are due to the improved interfacial adhesion between the dispersed phase (PP) and matrix phase (PS). The improvement in miscibility of the PS/PP blend with the addition of SEBS is supported by DMA analysis. This showed that the 60/40 PS/PP blends possess two endothermic peaks whereas 60/40/25 PS/PP/SEBS blends have a single endothermic peak at 102 °C, indicating that they have an improved miscibility. The effectiveness of SEBS in enhancing the blends depends on the blend composition. A significant improvement was observed upon addition of more than 10 phr of SEBS into the 70/30 and 60/40 PS/PP blends, but not much improvement in the case of the 90/10 and 80/20 PS/PP blends. However, a higher SEBS content is more effective at higher PS contents, as illustrated by the 90/10/25 PS/PP/SEBS blends having higher impact strengths than 60/40/25 PS/PP/SEBS. The optimum blend, based on achieving a balance between toughness (impact strength) and stiffness (flexural modulus), is 90/10/25 PS/PP/SEBS, followed by 80/20/25 PS/PP/SEBS.


RSC Advances ◽  
2015 ◽  
Vol 5 (19) ◽  
pp. 14592-14602 ◽  
Author(s):  
Rui Dou ◽  
Chao Shen ◽  
Bo Yin ◽  
Ming-bo Yang ◽  
Bang-hu Xie

The hierarchical core–shell structure in PA6/HDPE-g-MA/EPDM ternary blend was firstly formed using simple melt mixing. A super toughness PA6 ternary blends with HDPE-g-MA multi-core structure was obtained.


Author(s):  
D. Loretto ◽  
J. M. Gibson ◽  
S. M. Yalisove ◽  
R. T. Tung

The cobalt disilicide/silicon system has potential applications as a metal-base and as a permeable-base transistor. Although thin, low defect density, films of CoSi2 on Si(111) have been successfully grown, there are reasons to believe that Si(100)/CoSi2 may be better suited to the transmission of electrons at the silicon/silicide interface than Si(111)/CoSi2. A TEM study of the formation of CoSi2 on Si(100) is therefore being conducted. We have previously reported TEM observations on Si(111)/CoSi2 grown both in situ, in an ultra high vacuum (UHV) TEM and ex situ, in a conventional Molecular Beam Epitaxy system.The procedures used for the MBE growth have been described elsewhere. In situ experiments were performed in a JEOL 200CX electron microscope, extensively modified to give a vacuum of better than 10-9 T in the specimen region and the capacity to do in situ sample heating and deposition. Cobalt was deposited onto clean Si(100) samples by thermal evaporation from cobalt-coated Ta filaments.


2011 ◽  
Author(s):  
Percy L. Donaghay ◽  
Jan Rines ◽  
James Sullivan
Keyword(s):  

2020 ◽  
Vol 154 (2) ◽  
pp. 135-153 ◽  
Author(s):  
Gabriel García Caballero ◽  
Donella Beckwith ◽  
Nadezhda V. Shilova ◽  
Adele Gabba ◽  
Tanja J. Kutzner ◽  
...  

Abstract The concept of biomedical significance of the functional pairing between tissue lectins and their glycoconjugate counterreceptors has reached the mainstream of research on the flow of biological information. A major challenge now is to identify the principles of structure–activity relationships that underlie specificity of recognition and the ensuing post-binding processes. Toward this end, we focus on a distinct feature on the side of the lectin, i.e. its architecture to present the carbohydrate recognition domain (CRD). Working with a multifunctional human lectin, i.e. galectin-3, as model, its CRD is used in protein engineering to build variants with different modular assembly. Hereby, it becomes possible to compare activity features of the natural design, i.e. CRD attached to an N-terminal tail, with those of homo- and heterodimers and the tail-free protein. Thermodynamics of binding disaccharides proved full activity of all proteins at very similar affinity. The following glycan array testing revealed maintained preferential contact formation with N-acetyllactosamine oligomers and histo-blood group ABH epitopes irrespective of variant design. The study of carbohydrate-inhibitable binding of the test panel disclosed up to qualitative cell-type-dependent differences in sections of fixed murine epididymis and especially jejunum. By probing topological aspects of binding, the susceptibility to inhibition by a tetravalent glycocluster was markedly different for the wild-type vs the homodimeric variant proteins. The results teach the salient lesson that protein design matters: the type of CRD presentation can have a profound bearing on whether basically suited oligosaccharides, which for example tested positively in an array, will become binding partners in situ. When lectin-glycoconjugate aggregates (lattices) are formed, their structural organization will depend on this parameter. Further testing (ga)lectin variants will thus be instrumental (i) to define the full range of impact of altering protein assembly and (ii) to explain why certain types of design have been favored during the course of evolution, besides opening biomedical perspectives for potential applications of the novel galectin forms.


Materialia ◽  
2021 ◽  
Vol 15 ◽  
pp. 100993
Author(s):  
N. Armstrong ◽  
P.A. Lynch ◽  
P. Cizek ◽  
S.R. Kada ◽  
S. Slater ◽  
...  

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