1994
DOI: 10.1002/macp.1994.021950503
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Nuclear magnetic resonance spectroscopic characterization of carboxymethylcellulose

Abstract: Previous assignment of the signals in the spectra of carboxymethylcellulose, based on an incremental calculation and hence on low-molar-mass model substances, made determination of the partial degree of substitution fundamentally impossible because overlapping of the relevant signals was predicted. However, the methods of acid and enzymatic hydrolysis employed generate the monomer or a mixture of polymers, oligomers and monomers and hence a large number of end groups, which also influence the nuclear magnetic … Show more

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Cited by 88 publications
(45 citation statements)
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“…The peak at ı 82.44 corresponds to C 4 and the peak at ı 102.71 belongs to C 1 . More importantly, the 13 C NMR peak that appeared at ı 178.13 corresponds to the COO-group [26,37] and thus confirms that the LiCMC has been successfully synthesized. For comparison purposes, NaCMC (Calbiochem) was also analysed by 1 H NMR and 13 C NMR and the same peaks were observed.…”
Section: Synthesis and Characterization Of Licmcmentioning
confidence: 79%
“…The peak at ı 82.44 corresponds to C 4 and the peak at ı 102.71 belongs to C 1 . More importantly, the 13 C NMR peak that appeared at ı 178.13 corresponds to the COO-group [26,37] and thus confirms that the LiCMC has been successfully synthesized. For comparison purposes, NaCMC (Calbiochem) was also analysed by 1 H NMR and 13 C NMR and the same peaks were observed.…”
Section: Synthesis and Characterization Of Licmcmentioning
confidence: 79%
“…The determination of the pattern of functionalization of polysaccharides on the level of the AGU is usually carried out by NMR spectroscopy [9,10,13]. This can either be done by 13 C-NMR spectroscopic measurements on the intact polymer or by 1 H-NMR spectroscopy on the hydrolytically degraded sample.…”
Section: Determination Of the Functionalization Pattern Within The Anmentioning
confidence: 99%
“…The 1 H-NMR analyses were carried out as described [13] prepared using a new synthesis concept via a reactive microstructure revealed a high DS achieved in a one-step synthesis as well as a nonstatistic distribution of carboxymethyl groups along the chain. A significant amount of 2,3,4,6-tetra-O-functionalization, caused by the branched structure of starch, was found.…”
Section: Measurementsmentioning
confidence: 99%
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“…It has a number of sodium carboxymethyl groups (CH 2 COONa), introduced into the cellulose molecule, which promote water solubility. The three parameters that control the various properties of CMC are as follows; molecular weight of the polymer, average number of carboxyl content per anhydroglucose unit, and the distribution of carboxylmethyl group substituents along the polymer chains [5][6][7] During the past few years, many researchers have paid considerable attention to the study of carboxymethyl cellulose due to this material is an important industrial polymer which give a wide range of applications such as drag reduction, detergents, textiles, paper, foods, adhesives, paints, pharmaceutics, and oil well drilling operation. [8][9][10][11][12][13][14][15] In textiles industrial, CMC is used in the printing paste as a thickener and a emulsifier which significantly improve the vividness of printing, and improve the stability of the color paste.…”
Section: Introductionmentioning
confidence: 99%