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Stoichiometry and stability of cellulose-hydrazine complexes

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Abstract

Highly crystalline cellulose samples from green algae (cellulose I) and mercerized ramie (cellulose II) were treated with anhydrous hydrazine and the resulting complexes were analyzed by synchrotron X-ray diffraction and thermogravimetry. Cellulose I-hydrazine complex could be fully described by a two-chain monoclinic unit cell, a = 0.879 nm, b = 1.076 nm, c = 1.038 nm, and γ = 122.0°, with space group P21. Cellulose II-hydrazine complex prepared from mercerized ramie gave a different two-chain monoclinic unit cell, a = 1.042 nm, b = 1.046 nm, c = 1.038 nm, γ = 129.7°, also with space group P21. Though having different crystal structures, the number of hydrazine molecules per glucopyranoside residue was 0.82 for cellulose I-complex and 0.93 for cellulose II-complex, probable stoichiometric value of 1.0. Hydrazine could be extracted from the complexes by organic solvents retaining the crystalline orders, resulting in the allomorphic conversion to cellulose IIII and cellulose IIIII, both having non-staggered chain arrangements. These features are similar to those of cellulose-ethylenediamine complexes.

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Acknowledgments

The synchrotron radiation experiments were performed at SPring-8 with the approval of the Japan Synchrotron Research Institute (JASRI). This study was partly supported by a Grant-in-Aid for Scientific Research (Nos. 18780131).

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Correspondence to Masahisa Wada.

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Hydrazine is highly toxic, flammable, and unstable colorless liquid.

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Su, X., Kimura, S., Wada, M. et al. Stoichiometry and stability of cellulose-hydrazine complexes. Cellulose 18, 531–537 (2011). https://doi.org/10.1007/s10570-011-9505-3

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  • DOI: https://doi.org/10.1007/s10570-011-9505-3

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