Control of thermal degradation of polylactide (PLA)-clay nanocomposites using chain extenders

被引:266
作者
Najafi, N. [1 ]
Heuzey, M. C. [1 ]
Carreau, P. J. [1 ]
Wood-Adams, Paula M. [2 ]
机构
[1] Ecole Polytech, Ctr Appl Res Polymers & Composites, CREPEC, Dept Chem Engn, Montreal, PQ, Canada
[2] Concordia Univ, Ctr Appl Res Polymers & Composites, CREPEC, Dept Mech & Ind Engn, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Polylactide; Thermal degradation; Chain extender; Nanocomposite; POLY(LACTIC ACID); SILICATE NANOCOMPOSITES; MELT RHEOLOGY; MOLECULAR-STRUCTURE; CARBOXYL; STABILIZATION; POLYESTERS; EXTENSION;
D O I
10.1016/j.polymdegradstab.2012.01.016
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The control of thermal degradation of polylactide (PLA) during processing is still a challenge for the industry. In addition, the presence of an organically modified clay intensifies the rate of PLA degradation and molecular weight (M-W) reduction. In this work, three different chain extenders: polycarbodiimide (PCDI), tris (nonyl phenyl) phosphite (TNPP) and Joncryl (R) ADR 4368, were incorporated into PLA and PLA-based nanocomposites containing 2 wt% clay (Cloisite (R) 30B) in an effort to control thermal degradation. The thermal and rheological properties of the PLA and PLA nanocomposites with and without chain extender were investigated. Thermogravimetric analysis showed an increase in the onset temperature for thermal degradation after the incorporation of PCDI (2 wt%), TNPP (1 wt%), or Joncryl (1 wt%) into the nanocomposite. The theological results revealed that the addition of such a concentration of chain extender had a profound effect on the degradation and even increased the molecular weight in some cases. The mechanism of stabilization is most likely chain extension that results in the formation of longer linear chains in the PCDI and TNPP-modified nanocomposites, and a long chain branched (LCB) structure in Joncryl-based nanocomposites. It was found that Joncryl was the most efficient chain extender among the ones used in this study. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:554 / 565
页数:12
相关论文
共 43 条
  • [1] Synthesis of polylactic acid by direct polycondensation under vacuum without catalysts, solvents and initiators
    Achmad, Feerzet
    Yamane, Kenji
    Quan, Shi
    Kokugan, Takao
    [J]. CHEMICAL ENGINEERING JOURNAL, 2009, 151 (1-3) : 342 - 350
  • [3] Polymer-layered silicate nanocomposites: Preparation, properties and uses of a new class of materials
    Alexandre, Michael
    Dubois, Philippe
    [J]. Materials Science and Engineering: R: Reports, 2000, 28 (1-2) : 1 - 63
  • [4] Bikiaris DN, 1996, J POLYM SCI POL CHEM, V34, P1337, DOI 10.1002/(SICI)1099-0518(199605)34:7<1337::AID-POLA22>3.0.CO
  • [5] 2-9
  • [6] Free radical branching of polylactide by reactive extrusion
    Carlson, D
    Dubois, P
    Nie, L
    Narayan, R
    [J]. POLYMER ENGINEERING AND SCIENCE, 1998, 38 (02) : 311 - 321
  • [7] Synthesis and characterization of biodegradable poly(L-lactide)/layered double hydroxide nanocomposites
    Chiang, Ming-Feng
    Wu, Tzong-Ming
    [J]. COMPOSITES SCIENCE AND TECHNOLOGY, 2010, 70 (01) : 110 - 115
  • [8] Phosphite stabilization effects on two-step melt-spun fibers of polylactide
    Cicero, JA
    Dorgan, JR
    Dec, SF
    Knauss, DM
    [J]. POLYMER DEGRADATION AND STABILITY, 2002, 78 (01) : 95 - 105
  • [9] Fundamental solution and single-chain properties of polylactides
    Dorgan, JR
    Janzen, J
    Knauss, DM
    Hait, SB
    Limoges, BR
    Hutchinson, MH
    [J]. JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2005, 43 (21) : 3100 - 3111
  • [10] Melt rheology of variable L-content poly(lactic acid)
    Dorgan, JR
    Janzen, J
    Clayton, MP
    Hait, SB
    Knauss, DM
    [J]. JOURNAL OF RHEOLOGY, 2005, 49 (03) : 607 - 619