Talita Nascimento, Marta Ramos-Andrés, Rui Galhano dos Santos, António Aguiar, Ana C. Marques
{"title":"木质素衍生的功能化单体在催化剂、溶剂和无压力条件下的温和酸性氧化过程","authors":"Talita Nascimento, Marta Ramos-Andrés, Rui Galhano dos Santos, António Aguiar, Ana C. Marques","doi":"10.1016/j.biombioe.2025.107949","DOIUrl":null,"url":null,"abstract":"<div><div>Lignoboost® (LB) Kraft lignin was subjected to a mild acidic oxidative depolymerization process under solvent-, catalyst-, and pressure-free conditions, achieving functionalized monomers with proportions of up to 79.4 % (w/w). This environmentally friendly method operates under naturally acidic conditions using only H<sub>2</sub>O and H<sub>2</sub>O<sub>2</sub>, ensuring a high concentration of LB in suspension (300 mg/mL) and taking advantage of its inherent protonated nature. Monomers were directly recovered through simple drying, eliminating the need for precipitation or purification steps. Comprehensive characterization was performed using ATR-FTIR, HP-SEC, TGA, EA, <sup>1</sup>H NMR, and <sup>31</sup>P NMR techniques. The weight-average molecular weight (<span><math><mrow><mover><mrow><mi>M</mi><mi>w</mi></mrow><mo>‾</mo></mover></mrow></math></span>) and polydispersity index (PDI) decreased significantly from 1985 g/mol and 2.91 to as low as 300 g/mol and 1.79, respectively, after 7 h at 55 °C. Operational conditions were tuned to selectively enhance specific functional groups: phenolic OH groups increased up to 5.17 mmol/g under shorter reaction times (60 °C, 3 h), while moderate temperatures and longer reaction times favored carboxylic OH groups (4.99 mmol/g at 55 °C for 7 h). Additionally, alkene (C=C) groups reached up to 81.52 % of total hydrogen content under the highest temperature conditions (65 °C for 2 h). This process not only enhances our understanding of concurrent functionalization and depolymerization mechanisms but also establishes a scalable and green methodology for producing functionalized monomers as precursors for sustainable bio-based polymers. These findings contribute to the development of green technologies for lignin valorization.</div></div>","PeriodicalId":253,"journal":{"name":"Biomass & Bioenergy","volume":"199 ","pages":"Article 107949"},"PeriodicalIF":5.8000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A mild acidic oxidative process for lignin-derived functionalized monomers under catalyst, solvent, and pressure-free conditions\",\"authors\":\"Talita Nascimento, Marta Ramos-Andrés, Rui Galhano dos Santos, António Aguiar, Ana C. Marques\",\"doi\":\"10.1016/j.biombioe.2025.107949\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Lignoboost® (LB) Kraft lignin was subjected to a mild acidic oxidative depolymerization process under solvent-, catalyst-, and pressure-free conditions, achieving functionalized monomers with proportions of up to 79.4 % (w/w). This environmentally friendly method operates under naturally acidic conditions using only H<sub>2</sub>O and H<sub>2</sub>O<sub>2</sub>, ensuring a high concentration of LB in suspension (300 mg/mL) and taking advantage of its inherent protonated nature. Monomers were directly recovered through simple drying, eliminating the need for precipitation or purification steps. Comprehensive characterization was performed using ATR-FTIR, HP-SEC, TGA, EA, <sup>1</sup>H NMR, and <sup>31</sup>P NMR techniques. The weight-average molecular weight (<span><math><mrow><mover><mrow><mi>M</mi><mi>w</mi></mrow><mo>‾</mo></mover></mrow></math></span>) and polydispersity index (PDI) decreased significantly from 1985 g/mol and 2.91 to as low as 300 g/mol and 1.79, respectively, after 7 h at 55 °C. Operational conditions were tuned to selectively enhance specific functional groups: phenolic OH groups increased up to 5.17 mmol/g under shorter reaction times (60 °C, 3 h), while moderate temperatures and longer reaction times favored carboxylic OH groups (4.99 mmol/g at 55 °C for 7 h). Additionally, alkene (C=C) groups reached up to 81.52 % of total hydrogen content under the highest temperature conditions (65 °C for 2 h). This process not only enhances our understanding of concurrent functionalization and depolymerization mechanisms but also establishes a scalable and green methodology for producing functionalized monomers as precursors for sustainable bio-based polymers. 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A mild acidic oxidative process for lignin-derived functionalized monomers under catalyst, solvent, and pressure-free conditions
Lignoboost® (LB) Kraft lignin was subjected to a mild acidic oxidative depolymerization process under solvent-, catalyst-, and pressure-free conditions, achieving functionalized monomers with proportions of up to 79.4 % (w/w). This environmentally friendly method operates under naturally acidic conditions using only H2O and H2O2, ensuring a high concentration of LB in suspension (300 mg/mL) and taking advantage of its inherent protonated nature. Monomers were directly recovered through simple drying, eliminating the need for precipitation or purification steps. Comprehensive characterization was performed using ATR-FTIR, HP-SEC, TGA, EA, 1H NMR, and 31P NMR techniques. The weight-average molecular weight () and polydispersity index (PDI) decreased significantly from 1985 g/mol and 2.91 to as low as 300 g/mol and 1.79, respectively, after 7 h at 55 °C. Operational conditions were tuned to selectively enhance specific functional groups: phenolic OH groups increased up to 5.17 mmol/g under shorter reaction times (60 °C, 3 h), while moderate temperatures and longer reaction times favored carboxylic OH groups (4.99 mmol/g at 55 °C for 7 h). Additionally, alkene (C=C) groups reached up to 81.52 % of total hydrogen content under the highest temperature conditions (65 °C for 2 h). This process not only enhances our understanding of concurrent functionalization and depolymerization mechanisms but also establishes a scalable and green methodology for producing functionalized monomers as precursors for sustainable bio-based polymers. These findings contribute to the development of green technologies for lignin valorization.
期刊介绍:
Biomass & Bioenergy is an international journal publishing original research papers and short communications, review articles and case studies on biological resources, chemical and biological processes, and biomass products for new renewable sources of energy and materials.
The scope of the journal extends to the environmental, management and economic aspects of biomass and bioenergy.
Key areas covered by the journal:
• Biomass: sources, energy crop production processes, genetic improvements, composition. Please note that research on these biomass subjects must be linked directly to bioenergy generation.
• Biological Residues: residues/rests from agricultural production, forestry and plantations (palm, sugar etc), processing industries, and municipal sources (MSW). Papers on the use of biomass residues through innovative processes/technological novelty and/or consideration of feedstock/system sustainability (or unsustainability) are welcomed. However waste treatment processes and pollution control or mitigation which are only tangentially related to bioenergy are not in the scope of the journal, as they are more suited to publications in the environmental arena. Papers that describe conventional waste streams (ie well described in existing literature) that do not empirically address ''new'' added value from the process are not suitable for submission to the journal.
• Bioenergy Processes: fermentations, thermochemical conversions, liquid and gaseous fuels, and petrochemical substitutes
• Bioenergy Utilization: direct combustion, gasification, electricity production, chemical processes, and by-product remediation
• Biomass and the Environment: carbon cycle, the net energy efficiency of bioenergy systems, assessment of sustainability, and biodiversity issues.