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Functional group formation/elimination in residual kraft lignin

Article Abstract:

Functional group formation and elimination have been studied in residual kraft lignin using 31P NMR. An unseen set of alkali-induced fragmentation and condensation reactions was seen. Residual kraft lignin was oxidized as a function of time and as a function of temperature with elevated temperatures, pressures and pHs. Oxidative demethoxylation reactions brought formation of catechols, likely reactive intermediates of the oxidation. Rate of carboxylic acid formation and guaiacyl phenol elimination was in two distinct phases, the first fast, the second slower.

Author: Argyropoulos, Dimitris S., Asgari, Faraj
Publisher: NRC Research Press
Publication Name: Canadian Journal of Chemistry
Subject: Chemistry
ISSN: 0008-4042
Year: 1998
Canada, Observations, Oxygen, Materials science, Bleaching, Chemical reaction, Rate of, Chemical kinetics, Carboxylic acids, Phosphorus, Phosphorus (Chemical element)

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Coupling P-31 NMR with the Mannich reaction for the quantitative analysis of lignin

Article Abstract:

Reactivity of lignin model compounds has been studied under Mannich conditions with formaldehyde and piperidine. The piperidinomethyl group was introduced quantitatively at sterically unhindered positions ortho to a phenolic hydroxyl when substrate could react under ambient conditions. Reliability of the technique was studied with a series of dissolved kraft lignins at different stages in delignification. Data were similar to those from permanganate oxidation.

Author: Argyropoulos, Dimitris S., Jiang, Zhi-Hua
Publisher: NRC Research Press
Publication Name: Canadian Journal of Chemistry
Subject: Chemistry
ISSN: 0008-4042
Year: 1998
Analysis

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On the formation of diphenylmethane structures in lignin under kraft, EMCC, and soda pulping conditions

Article Abstract:

Efforts have been made to establish the nature of formation of diphenylmethane moieties in lignin during conventional soda and kraft pulping conditions. Using 31P NMR spectroscopy, formation of phenolic hydroxyl groups of the diphenylmethane units can be followed. They can be identified and quantified. Experimentation has indicated that diphenylmethanes form in greater amounts in conventional pulping than in EMCC pulping, when the kappa number is the same.

Author: Ahvazi, Behzad C., Pageau, Gerry, Argyropoulos, Dimitris S.
Publisher: NRC Research Press
Publication Name: Canadian Journal of Chemistry
Subject: Chemistry
ISSN: 0008-4042
Year: 1998
Methods, Production processes, Spectrum analysis, Spectroscopy, Kraft paper, Kraft papers, Soda pulping process, Soda pulping

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Subjects list: Research, Usage, Equipment and supplies, Wood pulp industry, Phenols, Phenols (Class of compounds), Nuclear magnetic resonance spectroscopy, Lignin, Pulp industry, Wood-pulp, Wood pulp, Chemistry, Wood, Industrial chemistry
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