Thermoplastic polyester amides derived from oleic acid

被引:49
|
作者
Zuo, Jiaqing [1 ]
Li, Shaojun [1 ]
Bouzidi, Laziz [1 ]
Narine, Suresh S. [1 ,2 ]
机构
[1] Trent Univ, Trent Biomat Res Program, Dept Phys & Astron, Peterborough, ON K9J 7B8, Canada
[2] Trent Univ, Trent Biomat Res Program, Dept Chem, Peterborough, ON K9J 7B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Lipid-based polyester amide; Ester to amide ratio; Thermal and mechanical properties; X-RAY-SCATTERING; CRYSTALLIZED SYNDIOTACTIC POLYSTYRENE; SURFACE COATING APPLICATIONS; NAHAR SEED OIL; POLY(ESTER AMIDE)S; EPSILON-CAPROLACTONE; PHYSICAL-PROPERTIES; GAMMA-FORM; AMINO-ACID; POLY(METHYL METHACRYLATE);
D O I
10.1016/j.polymer.2011.08.002
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Three lipid-based Polyester Amides (PEAS) with varying ratios of ester and amide linkages were synthesized. Oleic acid was used as the starting material to produce the intermediates, characterized by MS and NMR, used for polymerization. PEAs were characterized by FTIR and GPC. The PEAs were constrained to have similar number average molecular weights, in the 2 x 10(4) range, thereby enabling comparison of their physical properties from a structural perspective. The thermal behavior of the polymers was assessed by DSC. DMA and TGA. Thermal degradation was not affected by ester/amide ratios, but T(g) increased non-linearly with decreasing ester/amide ratios and correlated with hydrogen-bond density and repeating unit chain length. Crystallinity was studied by XRD and DSC. Degree of crystallization and multiple melting behavior as a function of cooling kinetics were explained well by hydrogen-bond density, repeating unit chain length and density of ester moieties. Mechanical properties were investigated by DMA and Tensile Analysis, with a non-linear increase of storage and tensile moduli recorded as a function of decreasing ester/amide ratios. The findings suggest how approaches to the synthesis of lipid-based PEAs can be targeted to the delivery of specific physical properties. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4503 / 4516
页数:14
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