Polymer Science & Engineering Division, CSIR-National Chemical Laboratory, Pune 411008, India.
NMR Resource Center, Organic Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India.
Carbohydr Polym. 2014 Nov 26;113:615-23. doi: 10.1016/j.carbpol.2014.07.056. Epub 2014 Aug 1.
Cellulose-I swells considerably in phosphoric acid, and converts to amorphous cellulose via a cellulose-II transition state. Controlled oxidation of cellulose-I to 6-carboxycellulose (6 CC) using HNO3-H3PO4-NaNO2 oxidation system led to the selective production of 6 CC's of varying carboxyl contents (1.7-22%) as well as various shapes and sizes (macro-sized fibrils of several micron length and/or spherical nanoparticles of 25-35 nm), depending on the reaction conditions. 6 CC's having less than 14% carboxyl content were largely in cellulose-II form (WAXRD values in-between cellulose I and cellulose II), whereas at 14-22% the 6 CC's were largely amorphous; only trace crystallinity was observed at 19% and 22% carboxyl 6 CC. Spherical nanoparticles retained a high degree of crystallinity having cellulose-I structure, whereas the macro-sized fibrils were largely converted to cellulose-II structure. Analysis by WAXRD as well as by CP-MAS (13)C NMR studies gave similar conclusions. Reduced molecular weight with progressive oxidation, including presence of oligomers, was also evident from an increase in the reducing-end carbon peak at ∼ 92 ppm. For high oxidation levels (>14%) the NMR 92-96 ppm peaks disappeared on extracting with dilute alkali, due to soluble oligomers being removed.
纤维素-I 在磷酸中会发生显著膨胀,并通过纤维素-II 过渡态转化为无定形纤维素。使用 HNO3-H3PO4-NaNO2 氧化体系将纤维素-I 可控氧化为 6-羧基纤维素(6CC),导致 6CC 的羧基含量(1.7-22%)以及各种形状和尺寸(几微米长的宏观纤维和/或 25-35nm 的球形纳米颗粒)具有选择性,这取决于反应条件。少于 14%羧基含量的 6CC 主要呈纤维素-II 形式(WAXRD 值在纤维素 I 和纤维素 II 之间),而在 14-22%时,6CC 主要为无定形;在 19%和 22%羧基 6CC 时仅观察到微量结晶度。球形纳米颗粒保留了纤维素-I 结构的高结晶度,而宏观纤维则主要转化为纤维素-II 结构。WAXRD 分析以及 CP-MAS(13)C NMR 研究得出了类似的结论。随着氧化程度的增加,分子量降低,包括低聚物的存在,也可以从约 92ppm 的还原端碳峰的增加中看出。对于高氧化水平(>14%),由于可溶低聚物被去除,用稀碱提取时 NMR 92-96ppm 峰消失。