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通过表面引发原子转移自由基聚合接枝 PBA 的纤维素微纤维,用于生物复合材料增强。

Cellulose microfibrils grafted with PBA via surface-initiated atom transfer radical polymerization for biocomposite reinforcement.

机构信息

Department of Chemical Engineering, University of New Brunswick, Fredericton, NB Canada.

出版信息

Biomacromolecules. 2011 Sep 12;12(9):3305-12. doi: 10.1021/bm200797a. Epub 2011 Aug 22.

Abstract

Immobilizing poly(butyl acrylate) (PBA) on cellulose microfibrils (CMFs) by atom transfer radical polymerization (ATRP) of butyl acrylate (BA) on the surface of 2-bromoisobutyryl-functionalized CMF generated highly hydrophobic microfibrils (CMF-PBA) with a hard core and a soft-shell structure. TGA and static water contact angle results suggested that the surfaces of the modified CMF samples were not completely covered by PBA chains until the molecular weight of grafts became sufficiently long. The GPC results indicated that the grafts with low molecular weight showed controlled/"living" characteristics of the surface-initiated ATRP; however, there existed more side reactions with the increase in molecular weights. Biocomposites consisting of polypropylene (PP) and CMF-PBA samples exhibited significantly improved compatibility, interface adhesion, and mechanical properties with the increase in PBA graft length. The findings confirmed that the longer grafts facilitated the better entanglement of PBA grafts with PP macromolecules and thus further improved the mechanical properties.

摘要

通过在 2-溴代异丁酰基功能化纤维素微纤维(CMF)表面上进行丁基丙烯酸酯(BA)的原子转移自由基聚合(ATRP),将聚(丙烯酸丁酯)(PBA)固定在纤维素微纤维(CMF)上,生成具有硬核心和软壳结构的高疏水性微纤维(CMF-PBA)。TGA 和静态水接触角结果表明,直到接枝的分子量变得足够长,改性 CMF 样品的表面才被 PBA 链完全覆盖。GPC 结果表明,低分子量接枝具有表面引发 ATRP 的受控/“活性”特征; 然而,随着分子量的增加,存在更多的副反应。由聚丙烯(PP)和 CMF-PBA 样品组成的生物复合材料表现出与 PBA 接枝长度增加相容性、界面附着力和机械性能显著提高。研究结果证实,较长的接枝有助于 PBA 接枝与 PP 大分子更好地缠结,从而进一步提高了机械性能。

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