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Depolymerization of polyesters in sub- and supercritical water

机译:超临界水中聚酯的解聚

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Depolymerization behavior polyesters (poly(ethylene terephthalate) (PET) and poly(ethylene 2,6-naphthalene dicarboxylate) (PEN)) in sub- and supercritical water was investigated for the purpose of monomer recycling. In case of the depolymerization of PET, the yield of terephthalic acid (TPA) increased to 90% with increasing reaction temperature up to 693 K while the maximum yield of ethylene glycol (EG) achieved was only 60% at 573 K. For PEN depolymerization, the yield of 2,6-naphthalene dicarboxylic acid (2,6-NPA) also increased to 97% with increasing reaction temperature up to 693 K and the maximum yield of EG obtained was also 60% at 573 K. The higher yield of 2,6-NPA than that of TPA was ascribed to the higher stability of 2,6-NPA than that of TPA. The lower yields of EG than the corresponding monomers (TPA and 2,6,-NPA) in the decomposition of the two kinds of polyesters were caused by the catalytic dehydroxylation of EG by protons derived from dicarboxylic acids.
机译:研究了分解性的聚酯(聚(乙二醇酯)(PET)和聚(乙烯2,6-萘二羧酸甲酯)(乙烯2,6-萘二羧酸二羧酸甲酯)(PEN)),用于单体回收的目的。在PET的解聚的情况下,对对苯二甲酸(TPA)的产率增加到90%,随着反应温度的增加,高达693 k,而乙二醇(例如)的最大收率仅为673K的乙二醇(例如)为60%,用于PEN解聚,2,6-萘二羧酸(2,6-NPA)的产率也增加至97%,随着反应温度的增加,高达693k,例如,例如,在573k时,例如获得的最大收率也为60%比TPA的2,6- NPA归因于2,6- NPA的稳定性高于TPA的稳定性。在两种聚酯的分解中,例如相应的单体(TPA和2,6,-NPA)的较低产量是由衍生自二羧酸的质子的催化脱羟基化引起的。

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