化学
相对粘度
还原粘度
粘度
热力学
特性粘度
液体粘度的温度依赖性
大气温度范围
溶剂
阿伦尼乌斯图
流变学
固有粘度
纤维素
活化能
分析化学(期刊)
色谱法
有机化学
聚合物
物理
作者
Martin Gericke,Kerstin Schlufter,Tim Liebert,Thomas Heinze,Tatiana Budtova
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2009-04-01
卷期号:10 (5): 1188-1194
被引量:266
摘要
Steady state shear flow of different types of cellulose (microcrystalline, spruce sulfite and bacterial) dissolved in 1-ethyl-3-methylimidazolium acetate was studied in a large range of concentrations (0−15%) and temperatures (0−100 °C). Newtonian flow was recorded for all experimental conditions; these viscosity values were used for detailed viscosity−concentration and viscosity−temperature analysis. The exponent in the viscosity−concentration power law was found to be around 4 for temperatures from 0 to 40 °C, which is comparable with cellulose dissolved in other solvents, and around 2.5−3 for 60−100 °C. Intrinsic viscosities of all celluloses decreased with temperature, indicating a drop in solvent thermodynamic quality with heating. The data obtained can be reduced to a master plot of viscosity versus (concentration × intrinsic viscosity) for all celluloses studied in the whole temperature range. Mark−Houwink exponents were determined: they were lower than that for cellulose dissolved in LiCl/N,N-dimethylacetamide at 30 °C and close to θ-value. Viscosity−inverse temperature plots showed a concave shape that is dictated by solvent temperature dependence. The values of the activation energies calculated within Arrhenius approximation are in-line with those obtained for cellulose of comparable molecular weights in other solvents.
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