In situ melt grafting in carbon black/polyolefin composites and its influence on conductive performance

2004 ◽  
Vol 53 (7) ◽  
pp. 944-950 ◽  
Author(s):  
Yan Hui Hou ◽  
Ming Qiu Zhang ◽  
Min Zhi Rong
Keyword(s):  
2003 ◽  
Vol 778 ◽  
Author(s):  
Rajdip Bandyopadhyaya ◽  
Weizhi Rong ◽  
Yong J. Suh ◽  
Sheldon K. Friedlander

AbstractCarbon black in the form of nanoparticle chains is used as a reinforcing filler in elastomers. However, the dynamics of the filler particles under tension and their role in the improvement of the mechanical properties of rubber are not well understood. We have studied experimentally the dynamics of isolated nanoparticle chain aggregates (NCAs) of carbon made by laser ablation, and also that of carbon black embedded in a polymer film. In situ studies of stretching and contraction of such chains in the transmission electron microscope (TEM) were conducted under different maximum values of strain. Stretching causes initially folded NCA to reorganize into a straight, taut configuration. Further stretching leads to either plastic deformation and breakage (at 37.4% strain) or to a partial elastic behavior of the chain at small strains (e.g. 2.3% strain). For all cases the chains were very flexible under tension. Similar reorientation and stretching was observed for carbon black chains embedded in a polymer film. Such flexible and elastic nature of NCAs point towards a possible mechanism of reinforcement of rubber by carbon black fillers.


2017 ◽  
Vol 266 ◽  
pp. 172-176
Author(s):  
Pattarawadee Maijan ◽  
Nitinart Saetung ◽  
Wisut Kaewsakul

Mixing behaviors of the compounds filled with different reinforcing fillers were studied in correlation with compound and vulcanizate properties. Four filler systems were used including: 1) silica plus small amount of silane coupling agent; 2) carbon black; 3) pre-modified silica; and 4) silica+silane-carbon black mixed one. The results have shown that silica provides longer optimum cure time and shorter cure rate than carbon black due to accelerator adsorption on silica surface. In addition, owing to highly polar nature on silica surface the silica-based compounds show rather high viscosity, attributed to stronger filler-filler interaction as can be confirmed by Payne effect and reinforcement index. However, the commercial surface treatment or pre-modified form of silica shows superior properties than in-situ modification of silica by silane during mixing, while it gives comparable properties to carbon black-based compound. Tensile properties of vulcanizates show a good correlation with the basic properties of their compounds.


2015 ◽  
Vol 73 (4) ◽  
pp. 1085-1101 ◽  
Author(s):  
Seyedeh Alaleh Sadrani ◽  
S. A. Ahmad Ramazani ◽  
Seyedeh Elham Khorshidiyeh ◽  
Narges Jafari Esfad

2013 ◽  
Vol 20 (6) ◽  
Author(s):  
Xueli Wu ◽  
Jianhui Qiu ◽  
Peng Liu ◽  
Eiichi Sakai ◽  
Lin Lei

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.


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