On the degradation evolution equations of cellulose

被引:101
作者
Ding H.-Z. [1 ]
Wang Z.D. [1 ]
机构
[1] School of Electrical and Electronic Engineering, The University of Manchester, Manchester M60 1QD, Sackville Street
基金
英国工程与自然科学研究理事会;
关键词
Arrhenius activation energy; Cellulose; Degradation; Degree of polymerisation; Kinetics; Modelling; Percentage loss; Tensile strength; Time-temperature superposition;
D O I
10.1007/s10570-007-9166-4
中图分类号
学科分类号
摘要
Cellulose degradation is usually characterized in terms of either the chain scission number or the scission fraction of cellulose unit as a function of degree of polymerisation (DP) and cellulose degradation evolution equation is most commonly described by the well known Ekenstam equations. In this paper we show that cellulose degradation can be best characterized either in terms of the percentage DP loss or in terms of the percentage tensile strength (TS) loss. We present a new cellulose degradation evolution equation expressed in terms of the percentage DP loss and apply it for having a quantitative comparison with six sets of experimental data. We develop a new kinetic equation for the percentage TS loss of cellulose and test it with four sets of experimental data. It turns out that the proposed cellulose degradation evolution equations are able to explain the real experimental data of different cellulose materials carried out under a variety of experimental conditions, particularly the prolonged autocatalytic degradation in sealed vessels. We also develop a new method for predicting the degree of degradation of cellulose at ambient conditions by combining the master equation representing the kinetics of either percentage DP loss or percentage TS loss at the lowest experimental temperature with Arrhenius shift factor function. © Springer Science+Business Media B.V. 2007.
引用
收藏
页码:205 / 224
页数:19
相关论文
共 41 条
[1]  
Arney J.S., Noval C.L., Accelerated aging of paper. The influence of acidity on the relative contribution of oxygen-independent and oxygen-dependent processes, Tappi J, 65, pp. 113-115, (1982)
[2]  
Baranski A., Lagan J.M., Lojewski T., The concept of mixed-control mechanisms and its applicability to paper degradation studies, E-PS, 3, pp. 1-4, (2006)
[3]  
Bouchard J., Methot M., Jordan B., The effects of ionizing radiation on the cellulose of woodfree paper, Cellulose, 13, pp. 601-610, (2006)
[4]  
Calvini P., The influence of levelling-off degree of polymerisation on the kinetics of cellulose degradation, Cellulose, 12, pp. 445-447, (2005)
[5]  
Calvini P., Gorassini A., On the rate of paper degradation: Lessons from the past, Restaurator, 27, 4, pp. 275-290, (2006)
[6]  
Chen S.L., Lucia L.A., Improved method for evaluation of cellulose degradation, J Wood Sci, 49, pp. 285-288, (2003)
[7]  
Daruwalla E.H., Narsian M.G., Detection and identification of acid-sensitive linkages in cellulose fiber substances, Tappi J, 49, 3, pp. 106-111, (1966)
[8]  
Ding H.-Z., Wang Z.D., Time-temperature superposition method for predicting the permanence of paper by extrapolating accelerated ageing data to ambient conditions, Cellulose, 14, pp. 171-181, (2007)
[9]  
Ekenstam A., The behaviour of cellulose in mineral acid solutions: Kinetic study of the decomposition of cellulose in acid solutions, BER, 69, pp. 540-553, (1936)
[10]  
Emsley A.M., Stevens G.C., Kinetics and mechanisms of the low temperature degradation of cellulose, Cellulose, 1, pp. 26-56, (1994)