CO2 Hydrogenation Catalysis

CO2 Hydrogenation Catalysis
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Описание книги

A guide to the effective catalysts and latest advances in CO2 conversion in chemicals and fuels  Carbon dioxide hydrogenation is one of the most promising and economic techniques to utilize CO2 emissions to produce value-added chemicals. With contributions from an international team of experts on the topic,  CO2 Hydrogenation Catalysis  offers a comprehensive review of the most recent developments in the catalytic hydrogenation of carbon dioxide to formic acid/formate, methanol, methane, and C2+ products.  The book explores the electroreduction of carbon dioxide and contains an overview on hydrogen production from formic acid and methanol. With a practical review of the advances and challenges in future CO2 hydrogenation research, the book provides an important guide for researchers in academia and industry working in the field of catalysis, organometallic chemistry, green and sustainable chemistry, as well as energy conversion and storage. This important book:  Offers a unique review of effective catalysts and the latest advances in CO2 conversion Explores how to utilize CO2 emissions to produce value-added chemicals and fuels such as methanol, olefins, gasoline, aromatics Includes the latest research in homogeneous and heterogeneous catalysis as well as electrocatalysis Highlights advances and challenges for future investigation Written for chemists, catalytic chemists, electrochemists, chemists in industry, and chemical engineers,  CO2 Hydrogenation Catalysis  offers a comprehensive resource to understanding how CO2 emissions can create value-added chemicals.

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Группа авторов. CO2 Hydrogenation Catalysis

Table of Contents

List of Tables

List of Illustrations

Guide

Pages

CO2 Hydrogenation Catalysis

Preface

1 Introduction

1.1 Direct Use of CO2

1.2 Chemicals from CO2 as a Feedstock

1.3 Application and Market Studies of CO2 Hydrogenation Products

1.3.1 Formic Acid/Formate

1.3.2 Methanol

1.3.3 Methanation

1.3.4 Energy Storage

1.4 Supply of Materials

1.4.1 CO 2 Supply

1.4.2 Energy and H2 Supply

1.5 Political Aspect: Tax

1.6 Conclusion and Perspectives

References

2 Homogeneously Catalyzed CO2 Hydrogenation to Formic Acid/Formate by Using Precious Metal Catalysts

2.1 Introduction

2.2 Ir Complexes

2.2.1 Ir Complexes with N,N‐ligands. 2.2.1.1 Tautomerizable N,N‐ligands with OH Groups

2.2.1.2 N,N‐ligands with NH Group

2.2.1.3 Tautomerizable N,N‐ligands with OH and NH Groups

2.2.1.4 Tautomerizable N,N‐ligands with Amide Group

2.2.2 Ir Complexes with C,N‐ and C,C‐ligands

2.2.3 Ir Complexes with Pincer Ligands

2.3 Ru Complexes

2.3.1 Ru Complexes with Phosphorous Ligands

2.3.2 Ru Complexes with N,N‐ and N,O‐ligands

2.3.3 Ru Complexes with Pincer Ligands

2.4 Rh Complexes

2.5 Summary and Conclusions

References

3 Homogeneously Catalyzed CO2 Hydrogenation to Formic Acid/Formate with Non‐precious Metal Catalysts

3.1 Introduction

3.2 Iron‐Catalyzed CO2 Hydrogenation

3.2.1 Non‐pincer‐Type Iron Complexes

3.2.2 Pincer‐Type Iron Complexes

3.3 Cobalt‐Catalyzed CO2 Hydrogenation

3.4 Nickel‐Catalyzed CO2 Hydrogenation

3.5 Copper‐Catalyzed CO2 Hydrogenation

3.6 Manganese‐Catalyzed CO2 Hydrogenation

3.7 Other Non‐precious Metals for CO2 Functionalization

3.8 Conclusions and Perspectives

References

4 Catalytic Homogeneous Hydrogenation of CO2 to Methanol

4.1 Carbon Recycling and Methanol in the Early Twenty‐First Century

4.2 Heterogeneous Catalysis for CO2 to Methanol

4.3 Homogeneous Catalysis – An Alternative for CO2 to Methanol. 4.3.1 Benefits of Homogeneous Catalysis

4.3.2 CO 2 Hydrogenation to Methanol Through Different Routes

4.3.3 The First Homogeneous System for CO2 Reduction to Methanol

4.3.4 Indirect CO2 Hydrogenation

4.3.5 Direct CO2 Hydrogenation

4.3.5.1 Through Formate Esters

4.3.5.2 Through Oxazolidinone or Formamides

4.3.6 CO 2 to Methanol via Formic Acid Disproportionation

4.4 Conclusion

References

5 Theoretical Studies of Homogeneously Catalytic Hydrogenation of Carbon Dioxide and Bioinspired Computational Design of Base‐Metal Catalysts

5.1 Introduction

5.2 H 2 Activation and CO2 Insertion Mechanisms

5.2.1 Hydrogen Activation

5.2.2 Insertion of CO2

5.3 Hydrogenation of CO2 to Formic Acid/Formate. 5.3.1 Catalysts with Precious Metals

5.3.2 Catalysts with Non‐noble Metals

5.4 Hydrogenation of CO2 to Methanol

5.5 Summary and Conclusions

References

6 Heterogenized Catalyst for the Hydrogenation of CO2 to Formic Acid or Its Derivatives

6.1 Introduction

6.2 Molecular Catalysts Heterogenized on the Surface of Grafted Supports

6.3 Molecular Catalysts Heterogenized on Coordination Polymers

6.4 Molecular Catalysts Heterogenized on Porous Organic Polymers

6.5 Concluding Remarks and Future Directions

References

7 Design and Architecture of Nanostructured Heterogeneous Catalysts for CO2 Hydrogenation to Formic Acid/Formate

7.1 Introduction

7.2 Unsupported Bulk Metal Catalysts

7.3 Unsupported Metal Nanoparticle Catalysts

7.3.1 Metal Nanoparticles Without Stabilizers

7.3.2 Metal Nanoparticles Stabilized by Ionic Liquids

7.3.3 Metal Nanoparticles Stabilized by Reverse Micelles

7.4 Supported Metal Nanoparticle Catalysts

7.4.1 Metal Nanoparticles Supported on Carbon‐Based Materials

7.4.2 Metal Nanoparticles Supported on Nitrogen‐Doped Carbon

7.4.3 Metal Nanoparticles Supported on Al2O3

7.4.4 Metal Nanoparticles Supported on TiO2

7.4.5 Metal Nanoparticles Supported on Surface‐Functionalized Materials

7.5 Embedded Single‐Atom Catalysts

7.6 Summary and Conclusions

References

8 Heterogeneously Catalyzed CO2 Hydrogenation to Alcohols

8.1 Introduction

8.2 CO 2 Hydrogenation to Methanol – Past to Present. 8.2.1 Syngas to Methanol

8.2.2 CO 2 to Methanol

8.2.3 Thermodynamic Consideration – Chemical and Phase Equilibria

8.2.4 Catalyst Developments

8.2.5 Active Sites and Reaction Mechanisms: The Case of Cu/ZnO Catalysts

8.2.6 Beyond Industrial Cu/ZnO/Al2O3 Catalysts

8.3 CO 2 Hydrogenation to Ethanol and Higher Alcohols – Past to Present. 8.3.1 Background

8.3.2 Catalysts, Active Sites, and Reaction Mechanisms

8.3.2.1 Modified‐Methanol Synthesis Catalyst

8.3.2.2 Modified Fischer–Tropsch Catalysts

8.3.2.3 Rhodium‐Based Catalysts

8.3.2.4 Modified Molybdenum‐Based Catalysts

8.4 Summary

References

9 Homogeneous Electrocatalytic CO2 Hydrogenation

9.1 CO 2 Reduction to C─H Bond‐Containing Compounds: Formate or Formic Acid

9.1.1 Survey of Catalysts

9.1.1.1 Group 9 Metal Complexes

9.1.1.2 Group 8 Metal Complexes

9.1.1.3 Nickel Complexes

9.1.1.4 Iron and Iron/Molybdenum Clusters

9.1.2 Hydride Transfer Mechanisms in CO2 Reduction to Formate

9.1.2.1 Terminal Hydrides

9.1.2.2 Bridging Hydrides

9.1.3 Kinetic Factors in Catalyst Design

9.1.3.1 Roles of Metal–Ligand Cooperation

9.1.3.2 Roles of Multiple Metal–Metal Bonds

9.1.4 Thermochemical Considerations in Catalyst Design

9.1.4.1 Selectivity for Formate over H2 as a Function of Hydricity

9.1.4.2 Solvent Dependence of Hydricity

9.2 Prospects in Electrocatalysis: CO2 Reduction Beyond Formation of One C─H Bond

References

10 Recent Advances in Homogeneous Catalysts for Hydrogen Production from Formic Acid and Methanol

10.1 Introduction

10.2 Formic Acid Dehydrogenation

10.2.1 Organic Solvent Systems. 10.2.1.1 Ru

10.2.1.2 Ir

10.2.1.3 Fe

10.2.2 Aqueous Solution Systems. 10.2.2.1 Ru

10.2.2.2 Ir

10.3 Aqueous‐phase Methanol Dehydrogenation

10.3.1.1 Ir

10.3.1.2 Non‐precious Metals

10.4 Conclusion

References

Index

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Edited by

Yuichiro Himeda

.....

Yuichiro Himeda

National Institute of Advanced Industrial Science and Technology,

.....

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