可衍生木质素聚砜与双酚基聚砜的亲水性增强,具有潜在的水过滤应用价值

Jignesh S. Mahajan, Hoda Shokrollahzadeh Behbahani, Matthew D. Green, LaShanda T. J. Korley and Thomas H. Epps
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引用次数: 0

摘要

可衍生木质素芳烃(如极性甲氧基)中固有的功能性为改善聚砜(PSfs)的亲水性提供了潜在的机会,而无需传统 PSf 改性通常使用的额外加工步骤和苛刻试剂/条件。根据本文的测定,无需任何聚合后改性的可衍生木质素聚砜的亲水性高于同类石油基聚砜(商业/实验室合成),并且与文献报道的功能化双酚 A 聚砜的亲水性相似。重要的是,与文献报道的官能化双酚 A-PSfs 相比,木质素可衍生 PSfs 的热性能有所改善,这些生物可衍生 PSfs 的热性能接近普通非官能化 PSfs。特别是木质素可衍生 PSfs 的玻璃化转变温度(Tg)和失重 5% 的降解温度(Td5%)(Tg ∼ 165-170 °C,Td5% ∼ 400-425 °C)明显高于文献中典型的官能化双酚 A-PSfs 的玻璃化转变温度(Tg ∼ 110-160 °C,Td5% ∼ 240 °C)、Td5% ∼240-260°C),接近未改性的商业/实验室合成双酚 A/双酚 F-PSfs(Tg ∼180-185 °C,Td5% ∼420-510 °C)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Increased hydrophilicity of lignin-derivable vs. bisphenol-based polysulfones for potential water filtration applications†

Increased hydrophilicity of lignin-derivable vs. bisphenol-based polysulfones for potential water filtration applications†

Increased hydrophilicity of lignin-derivable vs. bisphenol-based polysulfones for potential water filtration applications†

The functionality inherent in lignin-derivable aromatics (e.g., polar methoxy groups) can provide a potential opportunity to improve the hydrophilicity of polysulfones (PSfs) without the need for the additional processing steps and harsh reagents/conditions that are typically used in conventional PSf modifications. As determined herein, lignin-derivable PSfs without any post-polymerization modification exhibited higher hydrophilicity than comparable petroleum-based PSfs (commercial/laboratory-synthesized) and also demonstrated similar hydrophilicity to functionalized BPA-PSfs reported in the literature. Importantly, the lignin-derivable PSfs displayed improved thermal properties relative to functionalized BPA-PSfs in the literature, and the thermal properties of these bio-derivable PSfs were close to those of common non-functionalized PSfs. In particular, the glass transition temperature (Tg) and degradation temperature of 5% weight loss (Td5%) of lignin-derivable PSfs (Tg ∼165–170 °C, Td5% ∼400–425 °C) were significantly higher than those of typical functionalized BPA-PSfs in the literature (Tg ∼110–160 °C, Td5% ∼240–260 °C) and close to those of unmodified, commercial/laboratory-synthesized BPA-/bisphenol F-PSfs (Tg ∼180–185 °C, Td5% ∼420–510 °C).

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