Description

Book Synopsis
Lignin Conversion Catalysis

Authoritative reference providing comprehensive knowledge on the lignin conversion process with recent developments of mechanisms and techniques

Lignin Conversion Catalysis: Transformation to Aromatic Chemicals covers the strategy, catalysis, and mechanisms of cleaving lignin linkages to aromatic chemicals and crucially elaborates on the specifics of multiple original lignins. Sample topics covered in the work include:

  • Lignin depolymerization, models, and techniques of various lignins by heterogeneous substrates (such as native lignins, Kraft lignins, and organosolv lignins)
  • Cleavage methods for lignins (such as oxidation and hydrogenation) as well as their main products (such as arenes, phenol, and acid)
  • Relationships among the strategy/method, catalyst, and mechanism when viewed from the cleavage order and the type of corresponding chemical bonds
  • Commercial components of lignin, a globally available raw material with many applications in drug design, polymers, and more

Organic chemists, polymer chemists, and chemical engineers can use the valuable information contained in Lignin Conversion Catalysis: Transformation to Aromatic Chemicals to get up to date on this new raw material and understand the various developments that have been made in the field to make it viable for industrial purposes.



Table of Contents
Part I Book introduction
1. Background and overview

Part II Understanding about the lignin
2. Lignin biosynthesis, structure, and physicochemistry properties
3. Lignin isolation and lignin pre-chemical modification
4. Lignin detection, quantification and structure characterization

Part III Lignin depolymerization: scientific questions, challenges and current progress
5. Scientific questions for lignin conversion and new biorefinery
6. Brief summary of methods for lignin depolymerization

Part IV Strategies review on lignin linkages cleavage involved in lignin depolymerization via the inverse disassembly analysis
7. The inverse disassembly analysis (IDA) method for classifying lignin conversion methods/strategies
8. Direct lignin C-Oar, ArO-Ar or C-Ar bonds cleavage without first activation of the adjacent chemical bonds
9. Lignin linkages cleavage beginning with phenolic hydroxyl group dehydrogenation or first aromatic rings activation
10. Lignin linkages cleavage beginning with C alpha-H or ArO-H heterolysis
11. Lignin linkages cleavage beginning with C alpha-OH bond heterolysis
12. Lignin linkages cleavage beginning with the activation of C alpha-H, C alpha-OH or C alpha O-H bonds via non-ionized routes
13. Lignin linkages cleavage beginning with C beta-H direct activation
14. Lignin linkages cleavage beginning with C gamma-H or C gammaO-H direct activation
15. Lignin depolymerization strategies considering fragments condensation

Lignin Conversion Catalysis: Transformation to

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    A Hardback by Chaofeng Zhang, Feng Wang

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      View other formats and editions of Lignin Conversion Catalysis: Transformation to by Chaofeng Zhang

      Publisher: Wiley-VCH Verlag GmbH
      Publication Date: Publication Date: 07/09/2022
      ISBN13: 9783527349739, 978-3527349739
      ISBN10: 3527349731

      Description

      Book Synopsis
      Lignin Conversion Catalysis

      Authoritative reference providing comprehensive knowledge on the lignin conversion process with recent developments of mechanisms and techniques

      Lignin Conversion Catalysis: Transformation to Aromatic Chemicals covers the strategy, catalysis, and mechanisms of cleaving lignin linkages to aromatic chemicals and crucially elaborates on the specifics of multiple original lignins. Sample topics covered in the work include:

      • Lignin depolymerization, models, and techniques of various lignins by heterogeneous substrates (such as native lignins, Kraft lignins, and organosolv lignins)
      • Cleavage methods for lignins (such as oxidation and hydrogenation) as well as their main products (such as arenes, phenol, and acid)
      • Relationships among the strategy/method, catalyst, and mechanism when viewed from the cleavage order and the type of corresponding chemical bonds
      • Commercial components of lignin, a globally available raw material with many applications in drug design, polymers, and more

      Organic chemists, polymer chemists, and chemical engineers can use the valuable information contained in Lignin Conversion Catalysis: Transformation to Aromatic Chemicals to get up to date on this new raw material and understand the various developments that have been made in the field to make it viable for industrial purposes.



      Table of Contents
      Part I Book introduction
      1. Background and overview

      Part II Understanding about the lignin
      2. Lignin biosynthesis, structure, and physicochemistry properties
      3. Lignin isolation and lignin pre-chemical modification
      4. Lignin detection, quantification and structure characterization

      Part III Lignin depolymerization: scientific questions, challenges and current progress
      5. Scientific questions for lignin conversion and new biorefinery
      6. Brief summary of methods for lignin depolymerization

      Part IV Strategies review on lignin linkages cleavage involved in lignin depolymerization via the inverse disassembly analysis
      7. The inverse disassembly analysis (IDA) method for classifying lignin conversion methods/strategies
      8. Direct lignin C-Oar, ArO-Ar or C-Ar bonds cleavage without first activation of the adjacent chemical bonds
      9. Lignin linkages cleavage beginning with phenolic hydroxyl group dehydrogenation or first aromatic rings activation
      10. Lignin linkages cleavage beginning with C alpha-H or ArO-H heterolysis
      11. Lignin linkages cleavage beginning with C alpha-OH bond heterolysis
      12. Lignin linkages cleavage beginning with the activation of C alpha-H, C alpha-OH or C alpha O-H bonds via non-ionized routes
      13. Lignin linkages cleavage beginning with C beta-H direct activation
      14. Lignin linkages cleavage beginning with C gamma-H or C gammaO-H direct activation
      15. Lignin depolymerization strategies considering fragments condensation

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