Characterization of polyurethane networks structure and properties based on rapeseed oil derived polyol

被引:65
|
作者
Fridrihsone, Anda [1 ]
Stirna, Uldis [1 ]
Lazdina, Brigita [1 ]
Misane, Marija [1 ]
Vilsone, Dzintra [1 ]
机构
[1] Latvian State Inst Wood Chem, Polymer Lab, LV-1006 Riga, Latvia
关键词
Rapeseed oil polyols; Polyurethane networks; Mechanical properties; Thermal properties; Cohesion energy density; Molecular weight between cross-links; MECHANICAL-PROPERTIES; BEHAVIOR;
D O I
10.1016/j.eurpolymj.2013.03.012
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyurethane (PU) networks were synthesized from rapeseed oil (RO) and triethanolamine (TEA) polyols, as well as from modified RO/TEA polyol with epsilon-caprolactone (CPL) and triethylene glycol (TEG) additives. The study was carried out to determine the impact of molecular weight between cross-links (M-c), urethane group concentration and dangling chain concentration on structure of PU networks, physical, mechanical and thermal properties. The M-c of PU networks was varied using isocyanates (4,4'-methylene diphenyldiisocyanate (MDI), polymeric MDI Suprasec 2651, a polymeric MDI Lupranate M20) separately or in a mixture; the functionality of isocyanates was changed in range from 2.0 to 2.7. Using The Fourier transform infra-red spectral analysis (FTIR-ATR) the impact of M-c and urethane group concentration on PU networks to form hydrogen bonds was determined. Hydrogen bonding index (HBI) was calculated using ratio C=O-b/C=O-free, parameter R was calculated using ratio NHb/NHfree. It was found out that with increasing M-c of PU networks, HBI and R also increases. Glass transition temperature (T-g) of PU networks was determined using differential scanning calorimetry (DSC). Using model compound bis(2-hydroxyethyl)methylamine (MDEA) for PU networks synthesis, it was discovered that long dangling chains from RO/TEA are screening polar groups within PU networks, thus H-bond formation is interfered and as a result T-g and tensile strength decreases significantly in PU networks obtained from RO/TEA polyols. The volume contraction (Delta upsilon) during PU-forming reaction is determined by using experimental densities of PU and raw material additive densities. Higher Delta upsilon was for PU networks with higher urethane group concentration and higher M-c. The cohesion energy density (CED) and Van der Waals volume (V-w) was calculated for groups in PU networks structure. There is a correlation between CED and tensile strength of the obtained PU. The thermal properties of PU networks were characterized using thermogravimetric analysis (TGA). The initial weight loss (5 wt.%) occurs at lower temperature with increasing M-c and urethane group concentration. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1204 / 1214
页数:11
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