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Biobased Structurally Compatible Polymer Blends Based on Lignin and Thermoplastic Elastomer Polyurethane as Carbon Fiber Precursors

机译:基于木质素和热塑性弹性体聚氨酯作为碳纤维前体的Biobased结构相容性聚合物共混物

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摘要

The production of carbon fibers based on lignin reduces the cost and the environmental impact associated with carbon fiber manufacturing. However, the melt processing of lignin as a carbon fiber precursor is challenging due to its brittleness and limited thermoplastic behavior. For this reason we produce biopolymer blends based on Alcell organosolv hardwood lignin, hydroxypropyl modified Kraft hardwood, and a thermoplastic elastomer polyurethane (TPU). Samples with TPU content greater than 30% showed excellent melt processability and carbonization yield (35% carbon yield for the samples containing 30% of TPU). The thermal properties were analyzed by differential scanning calorimetry, rheology and thermogravimetric analysis. Fourier infrared measurements were utilized to explain the lignin/TPU interactions which governed the thermal and rheological behavior of the blends. SEM analysis showed that the blends produce a homogeneous structure which was void free after carbonization. These structurally complementary biopolymeric blends should open up new avenues for lignin valorization and bring closer the realization of the production of carbon fibers from biosources.
机译:基于木质素的碳纤维的生产降低了与碳纤维制造相关的成本和环境影响。然而,由于其脆性和有限的热塑性行为,因此Lignin作为碳纤维前体的熔体加工是挑战性的。出于这个原因,我们基于Alcell Organosolv硬木木质素,羟丙基改性的牛皮制硬木和热塑性弹性体聚氨酯(TPU)产生生物聚合物混合物。 TPU含量大于30%的样品显示出优异的熔体加工性和碳化率(含有30%TPU的样品的碳产率为35%)。通过差分扫描量热法,流变学和热重分析分析热性质。傅里叶红外测量用于解释木质素/ TPU相互作用,其治理了混合物的热和流变行为。 SEM分析表明,共混物在碳化之后产生无空隙的均匀结构。这些结构互补的生物聚合物共混物应为木质素储存开辟新的途径,并更接近生物源的碳纤维的产生。

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