Cargando…

From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”

A new chemical modification protocol to generate N-lignins is presented, based on Indulin AT and Mg(2+)-lignosulfonate. The already known ammonoxidation reaction in liquid phase was used as a starting point and stepwise optimised towards a full solid-state approach. The “classical” liquid ammonoxida...

Descripción completa

Detalles Bibliográficos
Autores principales: Wurzer, Gerhild K., Bacher, Markus, Musl, Oliver, Kohlhuber, Nadine, Sulaeva, Irina, Kelz, Theres, Fackler, Karin, Bischof, Robert H., Hettegger, Hubert, Potthast, Antje, Rosenau, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034478/
https://www.ncbi.nlm.nih.gov/pubmed/36968046
http://dx.doi.org/10.1039/d3ra00691c
_version_ 1784911230219059200
author Wurzer, Gerhild K.
Bacher, Markus
Musl, Oliver
Kohlhuber, Nadine
Sulaeva, Irina
Kelz, Theres
Fackler, Karin
Bischof, Robert H.
Hettegger, Hubert
Potthast, Antje
Rosenau, Thomas
author_facet Wurzer, Gerhild K.
Bacher, Markus
Musl, Oliver
Kohlhuber, Nadine
Sulaeva, Irina
Kelz, Theres
Fackler, Karin
Bischof, Robert H.
Hettegger, Hubert
Potthast, Antje
Rosenau, Thomas
author_sort Wurzer, Gerhild K.
collection PubMed
description A new chemical modification protocol to generate N-lignins is presented, based on Indulin AT and Mg(2+)-lignosulfonate. The already known ammonoxidation reaction in liquid phase was used as a starting point and stepwise optimised towards a full solid-state approach. The “classical” liquid ammonoxidation products, the transition products from the optimization trials, as well as the “solid-state” products were comprehensively analysed and compared to the literature. The N-lignins obtained with the conventional ammonoxidation protocol showed the same properties as reported. Their molar mass distributions and the hydroxy group contents, hitherto not accessible due to solubility problems, were measured according to a recently reported protocol. N-Indulin showed an N-content up to 11 wt% and N-lignosulfonate up to 16 wt%. The transition experiments from liquid to solid-state gave insights into the influence of chemical components and reaction conditions. The use of a single chemical, the urea-hydrogen peroxide complex (UHP, “carbamide peroxide”), was sufficient to generate N-lignins with satisfying N-content. This chemical acts both as an N-source and as the oxidant. Following the optimization, a series of solid-state ammonoxidation tests were carried out. High N-contents of 10% in the case of Indulin and 11% in the case of lignosulfonate were obtained. By varying the ratio of UHP to lignin, the N-content can be controlled. Structural analysis showed that the N is organically bound to the lignin, similar to the “classical” ammonoxidation products obtained under homogeneous conditions. Overall, a new ammonoxidation protocol was developed which does not require an external gas supply nor liquids or dissolved reactants. This opens the possibility for carrying out the lignin modification in closed continuous reactor systems, such as extruders. The new, facile solid-state protocol will hopefully help N-lignins to find more consideration as a fertilizing material and in soil-improving materials.
format Online
Article
Text
id pubmed-10034478
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-100344782023-03-24 From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins” Wurzer, Gerhild K. Bacher, Markus Musl, Oliver Kohlhuber, Nadine Sulaeva, Irina Kelz, Theres Fackler, Karin Bischof, Robert H. Hettegger, Hubert Potthast, Antje Rosenau, Thomas RSC Adv Chemistry A new chemical modification protocol to generate N-lignins is presented, based on Indulin AT and Mg(2+)-lignosulfonate. The already known ammonoxidation reaction in liquid phase was used as a starting point and stepwise optimised towards a full solid-state approach. The “classical” liquid ammonoxidation products, the transition products from the optimization trials, as well as the “solid-state” products were comprehensively analysed and compared to the literature. The N-lignins obtained with the conventional ammonoxidation protocol showed the same properties as reported. Their molar mass distributions and the hydroxy group contents, hitherto not accessible due to solubility problems, were measured according to a recently reported protocol. N-Indulin showed an N-content up to 11 wt% and N-lignosulfonate up to 16 wt%. The transition experiments from liquid to solid-state gave insights into the influence of chemical components and reaction conditions. The use of a single chemical, the urea-hydrogen peroxide complex (UHP, “carbamide peroxide”), was sufficient to generate N-lignins with satisfying N-content. This chemical acts both as an N-source and as the oxidant. Following the optimization, a series of solid-state ammonoxidation tests were carried out. High N-contents of 10% in the case of Indulin and 11% in the case of lignosulfonate were obtained. By varying the ratio of UHP to lignin, the N-content can be controlled. Structural analysis showed that the N is organically bound to the lignin, similar to the “classical” ammonoxidation products obtained under homogeneous conditions. Overall, a new ammonoxidation protocol was developed which does not require an external gas supply nor liquids or dissolved reactants. This opens the possibility for carrying out the lignin modification in closed continuous reactor systems, such as extruders. The new, facile solid-state protocol will hopefully help N-lignins to find more consideration as a fertilizing material and in soil-improving materials. The Royal Society of Chemistry 2023-03-23 /pmc/articles/PMC10034478/ /pubmed/36968046 http://dx.doi.org/10.1039/d3ra00691c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wurzer, Gerhild K.
Bacher, Markus
Musl, Oliver
Kohlhuber, Nadine
Sulaeva, Irina
Kelz, Theres
Fackler, Karin
Bischof, Robert H.
Hettegger, Hubert
Potthast, Antje
Rosenau, Thomas
From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”
title From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”
title_full From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”
title_fullStr From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”
title_full_unstemmed From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”
title_short From liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “N-lignins”
title_sort from liquid to solid-state, solvent-free oxidative ammonolysis of lignins – an easy, alternative approach to generate “n-lignins”
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034478/
https://www.ncbi.nlm.nih.gov/pubmed/36968046
http://dx.doi.org/10.1039/d3ra00691c
work_keys_str_mv AT wurzergerhildk fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT bachermarkus fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT musloliver fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT kohlhubernadine fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT sulaevairina fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT kelztheres fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT facklerkarin fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT bischofroberth fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT hetteggerhubert fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT potthastantje fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins
AT rosenauthomas fromliquidtosolidstatesolventfreeoxidativeammonolysisofligninsaneasyalternativeapproachtogeneratenlignins