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马来酸酐和次磷酸钠与实木反应形成的化学键。

Chemical Bonds Formed in Solid Wood by Reaction with Maleic Anhydride and Sodium Hypophosphite.

作者信息

Kim Injeong, Antzutkin Oleg N, Shah Faiz Ullah, Karlsson Olov, Jones Dennis, Sandberg Dick

机构信息

Wood Science and Engineering, Luleå University of Technology, Forskargatan 1, 93177 Skellefteå, Sweden.

Chemical Engineering, Luleå University of Technology, 97187 Luleå, Sweden.

出版信息

Materials (Basel). 2024 Oct 2;17(19):4856. doi: 10.3390/ma17194856.

Abstract

The reaction of wood with maleic anhydride (MA) and sodium hypophosphite (SHP) has been identified as a viable modification method, with macroscopical properties indicating formation of cross-linking to explain the results. However, the chemical reaction between wood and the modification reagents has not been studied yet. To resolve this, the reaction was studied with solid-state C cross-polarization magic-angle-spinning (CP-MAS) and P MAS nuclear magnetic resonance (NMR) and X-ray photoelectron spectroscopy (XPS) to reveal the formation of bonds between wood components, MA and SHP during the treatments to explain the formation of cross-linking and the possible fixation of phosphorus in wood. XPS, solid state C and P MAS NMR revealed the maleation of wood in the absence of SHP, whilst its presence led to forming a succinic adduct observed through the C-P bond formation, as evidenced by the loss of the maleate C=C bonds at around 130 ppm and the upfield shift of the peak at 165-175 ppm, which was also significantly smoothed, as well as the increase in a peak at 26 ppm due to the reaction between the maleate group and SHP; however, the C-P-C bond could not be unambiguously rationalized from the obtained data. On the other hand, a resonance line at 16 ppm in P MAS NMR and the peaks in the XPS P 2p spectrum suggested the formation of a cross-linked structure at low concentrations of SHP, which was more likely to be phosphonate (C-P-O) than organophosphinic acid (C-P-C). The results herein provide a greater fundamental understanding of the mechanisms involved in the reaction of wood, MA and SHP, providing further scope for improved treatment systems in the future.

摘要

木材与马来酸酐(MA)和次磷酸钠(SHP)的反应已被确认为一种可行的改性方法,宏观性能表明形成了交联结构来解释这些结果。然而,木材与改性试剂之间的化学反应尚未得到研究。为了解决这个问题,采用固态碳交叉极化魔角旋转(CP-MAS)和磷MAS核磁共振(NMR)以及X射线光电子能谱(XPS)对该反应进行了研究,以揭示在处理过程中木材成分、MA和SHP之间键的形成,从而解释交联结构的形成以及磷在木材中可能的固定情况。XPS、固态碳和磷MAS NMR揭示了在没有SHP的情况下木材的马来酸化反应,而SHP的存在导致通过C-P键的形成形成了琥珀酸加合物,这可由130 ppm左右马来酸酯C=C键的消失、165 - 175 ppm处峰的高场位移(该峰也显著变平滑)以及由于马来酸酯基团与SHP反应导致的26 ppm处峰的增加所证明;然而,从获得的数据中无法明确合理化C-P-C键。另一方面,磷MAS NMR中16 ppm处的共振线和XPS P 2p光谱中的峰表明在低浓度SHP下形成了交联结构,这种结构更可能是膦酸酯(C-P-O)而不是有机次膦酸(C-P-C)。本文的结果为木材、MA和SHP反应所涉及的机制提供了更深入的基础理解,为未来改进处理系统提供了进一步的空间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f5/11477618/dae49c08584e/materials-17-04856-g001.jpg

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