Effect of clay type and polymer matrix on microstructure and tensile properties of PLA/LLDPE/clay nanocomposites

被引:23
作者
As'habi, Ladan [1 ]
Jafari, Seyed Hassan [1 ]
Khonakdar, Hossein Ali [2 ]
Kretzschmar, Bernd [3 ]
Wagenknecht, Udo [3 ]
Heinrich, Gert [3 ]
机构
[1] Univ Tehran, Sch Chem Engn, Coll Engn, Tehran 111554563, Iran
[2] Iran Polymer & Petrochem Inst, Dept Plast Proc, Tehran 14965115, Iran
[3] Leibniz Inst Polymer Res Dresden, Dept Proc, D-01069 Dresden, Germany
关键词
morphology; mechanical properties; polyolefins; blends; THERMAL-STABILITY; BLENDS; COMPATIBILIZATION; MORPHOLOGY; RHEOLOGY; BEHAVIOR; ACID);
D O I
10.1002/app.39209
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Polylactide (PLA)/linear low-density polyethylene (LLDPE), (PLA/LLDPE), blends and nanocomposites were prepared by melt mixing process with a view to fine tune the properties. Two different commercial-grade nanoclays, Cloisite (R) 30B (30B) and CloisiteVR 15A (15A) were used. A terpolymer of ethylene, butylacrylate (BA) and glycidylmethacrylate (GMA) was used as a reactive compatibilizer. The influence of type of clay on the morphology and mechanical properties of two PLA-rich and LLDPE-rich blend systems was studied. Morphological analysis using X-ray diffraction, transmission electron microscopy, and scanning electron microscopy revealed that the organoclay layers were dispersed largely at the interface of PLA/LLDPE. Decreasing the PLA content changed the morphology from droplet-in matrix to coarse co-continuous. In comparison with 30B, due to less affinity of 15A towards compatibilizer and PLA phase, the reduction of the size of dispersed phase was less than that of the equivalent 30B composites. The mechanical results demonstrated that the composites containing both types of organoclay exhibited higher modulus but lower elongation and tensile strength as compared to the neat blends. The injection molded nanocomposites were shown to have the sequential fracture behavior during tensile test. The tensile testing results on the neat blends and nanocomposites showed significant increase in elongation at break and decrease in the modulus as compared with the neat PLA. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:749 / 758
页数:10
相关论文
共 34 条
[1]
Toughening of polylactide by melt blending with linear low-density polyethylene [J].
Anderson, KS ;
Lim, SH ;
Hillmyer, MA .
JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 89 (14) :3757-3768
[2]
Tuning the processability, morphology and biodegradability of clay incorporated PLA/LLDPE blends via selective localization of nanoclay induced by melt mixing sequence [J].
As'habi, L. ;
Jafari, S. H. ;
Khonakdar, H. A. ;
Boldt, R. ;
Wagenknecht, U. ;
Heinrich, G. .
EXPRESS POLYMER LETTERS, 2013, 7 (01) :21-39
[3]
Morphological, rheological and thermal studies in melt processed compatibilized PA6/ABS/clay nanocomposites [J].
As'habi, L. ;
Jafari, S. H. ;
Khonakdar, H. A. ;
Baghaei, B. .
JOURNAL OF POLYMER RESEARCH, 2011, 18 (02) :197-205
[4]
An Investigation of Melt Rheology and Thermal Stability of Poly(lactic acid)/Poly(butylene succinate) Nanocomposites [J].
Bhatia, Amita ;
Gupta, Rahul K. ;
Bhattacharya, Sati N. ;
Choi, H. J. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2009, 114 (05) :2837-2847
[5]
Bucknall C. B., 1977, APPL SCI, P189
[6]
Cabedo L, 2006, MACROMOL SYMP, V233, P191, DOI [10.1002/masy.200690017, 10.1002/masy.200650124]
[7]
Compatibilization-like effect of reactive organoclay on the poly(L-lactide)/poly(butylene succinate) blends [J].
Chen, GX ;
Kim, HS ;
Kim, ES ;
Yoon, JS .
POLYMER, 2005, 46 (25) :11829-11836
[8]
Thermal stability of poly(L-lactide)/poly(butylene succinate)/clay nanocomposites [J].
Chen, GX ;
Yoon, JS .
POLYMER DEGRADATION AND STABILITY, 2005, 88 (02) :206-212
[9]
Morphological stability in injection-moulded high-density polyethylene/polyamide-6 blends [J].
Fellahi, S ;
Favis, BD ;
Fisa, B .
POLYMER, 1996, 37 (13) :2615-2626
[10]
Uneven distribution of nanoparticles in immiscible fluids: Morphology development in polymer blends [J].
Fenouillot, F. ;
Cassagnau, P. ;
Majeste, J. -C. .
POLYMER, 2009, 50 (06) :1333-1350