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Degree of polymerization cellulose

Heinze et al. found that DMSO in combination with tetrabutylammonium fluoride trihydrate dissolved cellulose (degree of polymerization < 650) within 15 min at room temperature [38]. They also demonstrated that homogeneous esterification of cellulose is possible in this solvent system. The applicability of this new solvent system to cellulose grafting has recently been proved by adoption of cyclic compounds such as lactones and N-carboxy a-amino acid anhydrides (NCAs) [39]. e-Caprolactone was facilely graft-polymerized on cellulose at a graft rate of 65% (per trunk weight of 100), and NCAs at over 100%, in the respective homogeneous reaction systems at < 60 °C. [Pg.109]

The change in cellulose degree of polymerization ys time using TFA-CH2CI2 (70 30 v/v) as solvent is shown in Table V. The decrease in D.P. is nominal, has essentially leveled off after 7 days and, as shown in Table II, the solution is anisotropic for at least 10 days. [Pg.188]

Hydrocelluloses are produced by the hydrolytic degradation of celluloses. They are similar to )8-celluloses and are also referred to as microcrystalline celluloses. If 5% of these degraded celluloses (degree of polymerization 100-200) is beaten into water with rapid stirring, a creamy substance is produced that is used in the foodstuff industry as a nondigestable thickener. The creamy consistency arises because of physical cross-linking of cellulose crystallites. [Pg.580]

Another solvent used to dissolve cellulose is a mixture of ammonia and copper, in what is known as the Bemberg process [73]. The Bemberg process is advantageous over the viscose process in that it is less stringent on cellulose degree of polymerization and concentration, and the process itself is relatively simpler. But the properties of the resultant fiber are inferior to the viscose rayon. Both processes suffer due to the pollutants produced and difficulty in... [Pg.701]

Cellulose is the main component of the wood cell wall, typically 40—50% by weight of the dry wood. Pure cellulose is a polymer of glucose residues joined by 1,4-P-glucosidic bonds. The degree of polymerization (DP) is variable and may range from 700 to 10,000 DP or more. Wood cellulose is more resistant to dilute acid hydrolysis than hemiceUulose. X-ray diffraction indicates a partial crystalline stmcture for wood cellulose. The crystalline regions are more difficult to hydrolyze than the amorphous regions because removal of the easily hydrolyzed material has Htde effect on the diffraction pattern. [Pg.321]

The viscosity range of CN products can be adjusted in advance by choosing the starting cellulose with an appropriate degree of polymerization (DP). A study of the different celluloses examined the impact of various cellulose properties, such as morphological factors (percent crystallinity, fiber length, and distribution), chemical composition (DP, ash content), and hemiceUulose and lignin content, on the nitration behaviors of cellulose (55). [Pg.266]

In the case of grinding, the cellulose fibers go over a state of fine fibrillation into a more or less powdery substance. This mechanical severance of cellulose may break main valence bonds and will, therefore, decrease its degree of polymerization. In addition, the crystal structure of cellulose fibers is nearly lost [32]. Grinding of the cellulose fibers also, appreciably increases its surface area. [Pg.536]

Bleached cotton stalk pulp is treated with different concentrations of ethylene diamine (50-100%) for 20 min. It is clear that the crystallinity index (CrI) of these treated pulps is decreased by increasing the concentration of ethylene diamine that is, the decrystallization increases. The degree of polymerization is nearly the same, but some increase is shown in the sample treated with 100% ethylene diamine. This indicates that 100% ethylene diamine may act as a dissolving agent for low degree of polymerization (DP) of cellulosic chains and hemicellulose. [Pg.536]

The properties of hydroxyethylcellulose are like those of methylcellulose except for the fact that there is little or no temperature effect on solubility. The degree of substitution required to impart water solubility will depend both upon the degree of polymerization of the cellulose and upon the uniformity of substitution. It is of interest... [Pg.309]


See other pages where Degree of polymerization cellulose is mentioned: [Pg.276]    [Pg.5]    [Pg.440]    [Pg.89]    [Pg.28]    [Pg.276]    [Pg.5]    [Pg.440]    [Pg.89]    [Pg.28]    [Pg.295]    [Pg.295]    [Pg.29]    [Pg.11]    [Pg.251]    [Pg.272]    [Pg.248]    [Pg.249]    [Pg.251]    [Pg.258]    [Pg.791]    [Pg.807]    [Pg.6]    [Pg.85]    [Pg.85]    [Pg.620]    [Pg.252]    [Pg.354]    [Pg.302]    [Pg.303]    [Pg.304]    [Pg.306]    [Pg.307]    [Pg.308]    [Pg.310]    [Pg.406]    [Pg.182]    [Pg.249]    [Pg.119]    [Pg.298]    [Pg.148]    [Pg.25]    [Pg.214]    [Pg.214]   
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See also in sourсe #XX -- [ Pg.179 ]

See also in sourсe #XX -- [ Pg.35 ]

See also in sourсe #XX -- [ Pg.30 , Pg.32 ]

See also in sourсe #XX -- [ Pg.662 ]




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