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Green polymerization methods [[electronic resource] ] : renewable starting materials, catalysis and waste reduction / / edited by Robert T. Mathers and Michael A.R. Meier
| Green polymerization methods [[electronic resource] ] : renewable starting materials, catalysis and waste reduction / / edited by Robert T. Mathers and Michael A.R. Meier |
| Pubbl/distr/stampa | Weinheim, Germany, : Wiley-VCH Verlag |
| Descrizione fisica | 1 online resource (381 p.) |
| Disciplina |
668.9
668.92 |
| Altri autori (Persone) |
MathersRobert T
MeierMichael A. R |
| Soggetto topico |
Polymerization - Environmental aspects
Chemical reactions - Environmental aspects |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-283-86965-9
3-527-63617-X 3-527-63618-8 3-527-63616-1 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Polymerization Methods; Contents; List of Contributors; Part I Introduction; 1 Why are Green Polymerization Methods Relevant to Society, Industry, and Academics?; 1.1 Status and Outlook for Environmentally Benign Processes; 1.2 Importance of Catalysis; 1.3 Brief Summaries of Contributions; References; Part II Integration of Renewable Starting Materials; 2 Plant Oils as Renewable Feedstock for Polymer Science; 2.1 Introduction; 2.2 Cross-Linked Materials; 2.3 Non-Cross-Linked Polymers; 2.3.1 Monomer Synthesis; 2.3.2 Polymer Synthesis; 2.4 Conclusion; References
3 Furans as Offsprings of Sugars and Polysaccharides and Progenitors of an Emblematic Family of Polymer Siblings3.1 Introduction; 3.2 First Generation Furans and their Conversion into Monomers; 3.2.1 Furfural and Derivatives; 3.2.2 Monomers from Furfural; 3.2.3 Hydroxymethylfurfural; 3.3 Polymers from Furfuryl Alcohol; 3.4 Conjugated Polymers and Oligomers; 3.5 Polyesters; 3.6 Polyamides; 3.7 Polyurethanes; 3.8 Furyl Oxirane; 3.9 Application of the Diels-Alder Reaction to Furan Polymers; 3.9.1 Linear Polymerizations; 3.9.2 Non-Linear Polymerizations; 3.9.3 Reversible Polymer Cross-Linking 3.9.4 Miscellaneous Systems3.10 Conclusions; References; 4 Selective Conversion of Glycerol into Functional Monomers via Catalytic Processes; 4.1 Introduction; 4.2 Conversion of Glycerol into Glycerol Carbonate; 4.3 Conversion of Glycerol into Acrolein/Acrylic Acid; 4.4 Conversion of Glycerol into Glycidol; 4.5 Oxidation of Glycerol to Functional Carboxylic Acid; 4.5.1 Catalytic Oxidation of Glycerol to Glyceric Acid; 4.5.2 Oxidative-Assisted Polymerization of Glycerol; 4.5.2.1 Cationic Polymerization; 4.5.2.2 Anionic Polymerization; 4.6 Conversion of Glycerol into Acrylonitrile 4.7 Selective Conversion of Glycerol into Propylene Glycol4.7.1 Conversion of Glycerol into Propylene Glycol; 4.7.1.1 Reaction in the Liquid Phase; 4.7.1.2 Reaction in the Gas Phase; 4.7.2 Conversion of Glycerol into 1,3-Propanediol; 4.8 Selective Coupling of Glycerol with Functional Monomers; 4.9 Conclusion; References; Part III Sustainable Reaction Conditions; 5 Monoterpenes as Polymerization Solvents and Monomers in Polymer Chemistry; 5.1 Introduction; 5.2 Monoterpenes as Monomers; 5.2.1 Terpenic Resins Overview; 5.2.2 Concepts of Cationic Olefin Polymerization 5.2.3 Cationic Polymerization of β-Pinene5.2.4 Cationic Polymerization of Dipentene; 5.2.5 Cationic Polymerization of α-Pinene; 5.2.6 Characteristics of Terpenic Resins; 5.2.7 Applications of Terpenic Resins; 5.2.8 Commercial Production and Markets of Terpenic Resins; 5.2.9 Environmental Aspects of Terpenic Resin Production; 5.3 Monoterpenes as Solvents and Chain Transfer Agents; 5.3.1 Possibilities for Replacing Petroleum Solvents; 5.3.2 Ring-Opening Polymerizations in Monoterpenes; 5.3.3 Metallocene Polymerizations in Monoterpenes; 5.4 Conclusion; Acknowledgments; References 6 Controlled and Living Polymerization in Water: Modern Methods and Application to Bio-Synthetic Hybrid Materials |
| Record Nr. | UNINA-9910130907303321 |
| Weinheim, Germany, : Wiley-VCH Verlag | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green polymerization methods [[electronic resource] ] : renewable starting materials, catalysis and waste reduction / / edited by Robert T. Mathers and Michael A.R. Meier
| Green polymerization methods [[electronic resource] ] : renewable starting materials, catalysis and waste reduction / / edited by Robert T. Mathers and Michael A.R. Meier |
| Pubbl/distr/stampa | Weinheim, Germany, : Wiley-VCH Verlag |
| Descrizione fisica | 1 online resource (381 p.) |
| Disciplina |
668.9
668.92 |
| Altri autori (Persone) |
MathersRobert T
MeierMichael A. R |
| Soggetto topico |
Polymerization - Environmental aspects
Chemical reactions - Environmental aspects |
| ISBN |
1-283-86965-9
3-527-63617-X 3-527-63618-8 3-527-63616-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Polymerization Methods; Contents; List of Contributors; Part I Introduction; 1 Why are Green Polymerization Methods Relevant to Society, Industry, and Academics?; 1.1 Status and Outlook for Environmentally Benign Processes; 1.2 Importance of Catalysis; 1.3 Brief Summaries of Contributions; References; Part II Integration of Renewable Starting Materials; 2 Plant Oils as Renewable Feedstock for Polymer Science; 2.1 Introduction; 2.2 Cross-Linked Materials; 2.3 Non-Cross-Linked Polymers; 2.3.1 Monomer Synthesis; 2.3.2 Polymer Synthesis; 2.4 Conclusion; References
3 Furans as Offsprings of Sugars and Polysaccharides and Progenitors of an Emblematic Family of Polymer Siblings3.1 Introduction; 3.2 First Generation Furans and their Conversion into Monomers; 3.2.1 Furfural and Derivatives; 3.2.2 Monomers from Furfural; 3.2.3 Hydroxymethylfurfural; 3.3 Polymers from Furfuryl Alcohol; 3.4 Conjugated Polymers and Oligomers; 3.5 Polyesters; 3.6 Polyamides; 3.7 Polyurethanes; 3.8 Furyl Oxirane; 3.9 Application of the Diels-Alder Reaction to Furan Polymers; 3.9.1 Linear Polymerizations; 3.9.2 Non-Linear Polymerizations; 3.9.3 Reversible Polymer Cross-Linking 3.9.4 Miscellaneous Systems3.10 Conclusions; References; 4 Selective Conversion of Glycerol into Functional Monomers via Catalytic Processes; 4.1 Introduction; 4.2 Conversion of Glycerol into Glycerol Carbonate; 4.3 Conversion of Glycerol into Acrolein/Acrylic Acid; 4.4 Conversion of Glycerol into Glycidol; 4.5 Oxidation of Glycerol to Functional Carboxylic Acid; 4.5.1 Catalytic Oxidation of Glycerol to Glyceric Acid; 4.5.2 Oxidative-Assisted Polymerization of Glycerol; 4.5.2.1 Cationic Polymerization; 4.5.2.2 Anionic Polymerization; 4.6 Conversion of Glycerol into Acrylonitrile 4.7 Selective Conversion of Glycerol into Propylene Glycol4.7.1 Conversion of Glycerol into Propylene Glycol; 4.7.1.1 Reaction in the Liquid Phase; 4.7.1.2 Reaction in the Gas Phase; 4.7.2 Conversion of Glycerol into 1,3-Propanediol; 4.8 Selective Coupling of Glycerol with Functional Monomers; 4.9 Conclusion; References; Part III Sustainable Reaction Conditions; 5 Monoterpenes as Polymerization Solvents and Monomers in Polymer Chemistry; 5.1 Introduction; 5.2 Monoterpenes as Monomers; 5.2.1 Terpenic Resins Overview; 5.2.2 Concepts of Cationic Olefin Polymerization 5.2.3 Cationic Polymerization of β-Pinene5.2.4 Cationic Polymerization of Dipentene; 5.2.5 Cationic Polymerization of α-Pinene; 5.2.6 Characteristics of Terpenic Resins; 5.2.7 Applications of Terpenic Resins; 5.2.8 Commercial Production and Markets of Terpenic Resins; 5.2.9 Environmental Aspects of Terpenic Resin Production; 5.3 Monoterpenes as Solvents and Chain Transfer Agents; 5.3.1 Possibilities for Replacing Petroleum Solvents; 5.3.2 Ring-Opening Polymerizations in Monoterpenes; 5.3.3 Metallocene Polymerizations in Monoterpenes; 5.4 Conclusion; Acknowledgments; References 6 Controlled and Living Polymerization in Water: Modern Methods and Application to Bio-Synthetic Hybrid Materials |
| Record Nr. | UNINA-9910830102403321 |
| Weinheim, Germany, : Wiley-VCH Verlag | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green polymerization methods [[electronic resource] ] : renewable starting materials, catalysis and waste reduction / / edited by Robert T. Mathers and Michael A.R. Meier
| Green polymerization methods [[electronic resource] ] : renewable starting materials, catalysis and waste reduction / / edited by Robert T. Mathers and Michael A.R. Meier |
| Pubbl/distr/stampa | Weinheim, Germany, : Wiley-VCH Verlag |
| Descrizione fisica | 1 online resource (381 p.) |
| Disciplina |
668.9
668.92 |
| Altri autori (Persone) |
MathersRobert T
MeierMichael A. R |
| Soggetto topico |
Polymerization - Environmental aspects
Chemical reactions - Environmental aspects |
| ISBN |
1-283-86965-9
3-527-63617-X 3-527-63618-8 3-527-63616-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Polymerization Methods; Contents; List of Contributors; Part I Introduction; 1 Why are Green Polymerization Methods Relevant to Society, Industry, and Academics?; 1.1 Status and Outlook for Environmentally Benign Processes; 1.2 Importance of Catalysis; 1.3 Brief Summaries of Contributions; References; Part II Integration of Renewable Starting Materials; 2 Plant Oils as Renewable Feedstock for Polymer Science; 2.1 Introduction; 2.2 Cross-Linked Materials; 2.3 Non-Cross-Linked Polymers; 2.3.1 Monomer Synthesis; 2.3.2 Polymer Synthesis; 2.4 Conclusion; References
3 Furans as Offsprings of Sugars and Polysaccharides and Progenitors of an Emblematic Family of Polymer Siblings3.1 Introduction; 3.2 First Generation Furans and their Conversion into Monomers; 3.2.1 Furfural and Derivatives; 3.2.2 Monomers from Furfural; 3.2.3 Hydroxymethylfurfural; 3.3 Polymers from Furfuryl Alcohol; 3.4 Conjugated Polymers and Oligomers; 3.5 Polyesters; 3.6 Polyamides; 3.7 Polyurethanes; 3.8 Furyl Oxirane; 3.9 Application of the Diels-Alder Reaction to Furan Polymers; 3.9.1 Linear Polymerizations; 3.9.2 Non-Linear Polymerizations; 3.9.3 Reversible Polymer Cross-Linking 3.9.4 Miscellaneous Systems3.10 Conclusions; References; 4 Selective Conversion of Glycerol into Functional Monomers via Catalytic Processes; 4.1 Introduction; 4.2 Conversion of Glycerol into Glycerol Carbonate; 4.3 Conversion of Glycerol into Acrolein/Acrylic Acid; 4.4 Conversion of Glycerol into Glycidol; 4.5 Oxidation of Glycerol to Functional Carboxylic Acid; 4.5.1 Catalytic Oxidation of Glycerol to Glyceric Acid; 4.5.2 Oxidative-Assisted Polymerization of Glycerol; 4.5.2.1 Cationic Polymerization; 4.5.2.2 Anionic Polymerization; 4.6 Conversion of Glycerol into Acrylonitrile 4.7 Selective Conversion of Glycerol into Propylene Glycol4.7.1 Conversion of Glycerol into Propylene Glycol; 4.7.1.1 Reaction in the Liquid Phase; 4.7.1.2 Reaction in the Gas Phase; 4.7.2 Conversion of Glycerol into 1,3-Propanediol; 4.8 Selective Coupling of Glycerol with Functional Monomers; 4.9 Conclusion; References; Part III Sustainable Reaction Conditions; 5 Monoterpenes as Polymerization Solvents and Monomers in Polymer Chemistry; 5.1 Introduction; 5.2 Monoterpenes as Monomers; 5.2.1 Terpenic Resins Overview; 5.2.2 Concepts of Cationic Olefin Polymerization 5.2.3 Cationic Polymerization of β-Pinene5.2.4 Cationic Polymerization of Dipentene; 5.2.5 Cationic Polymerization of α-Pinene; 5.2.6 Characteristics of Terpenic Resins; 5.2.7 Applications of Terpenic Resins; 5.2.8 Commercial Production and Markets of Terpenic Resins; 5.2.9 Environmental Aspects of Terpenic Resin Production; 5.3 Monoterpenes as Solvents and Chain Transfer Agents; 5.3.1 Possibilities for Replacing Petroleum Solvents; 5.3.2 Ring-Opening Polymerizations in Monoterpenes; 5.3.3 Metallocene Polymerizations in Monoterpenes; 5.4 Conclusion; Acknowledgments; References 6 Controlled and Living Polymerization in Water: Modern Methods and Application to Bio-Synthetic Hybrid Materials |
| Record Nr. | UNINA-9910840534803321 |
| Weinheim, Germany, : Wiley-VCH Verlag | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of transition metal polymerization catalysts [[electronic resource] /] / edited by Ray Hoff, Robert T. Mathers
| Handbook of transition metal polymerization catalysts [[electronic resource] /] / edited by Ray Hoff, Robert T. Mathers |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2010 |
| Descrizione fisica | 1 online resource (599 p.) |
| Disciplina | 668.9/2 |
| Altri autori (Persone) |
HoffRaymond E
MathersRobert T |
| Soggetto topico |
Polymerization
Transition metal catalysts Metathesis (Chemistry) |
| ISBN |
1-282-81669-1
9786612816697 0-470-50443-9 0-470-50442-0 |
| Classificazione |
VH 7900
VH 9700 VK 8000 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
HANDBOOK OF TRANSITION METAL POLYMERIZATION CATALYSTS; CONTENTS; Introduction; About the Authors; 1 Commercially Available Metal Alkyls and Their Use in Polyolefin Catalysts; 2 Porous Silica in Transition Metal Polymerization Catalysts; 3 Computational Modeling of Polymerization Catalysts; 4 Scale-Up of Catalyst Recipes to Commercial Production; 5 Commercialization of Olefin Polymerization Catalysts: Model for Success; 6 Supported Magnesium/Titanium-Based Ziegler Catalysts for Production of Polyethylene; 7 Stereospecific α-Olefin Polymerization with Heterogeneous Catalysts
8 MgCl(2)-Supported TiCl(4) Catalysts for Production of Morphology-Controlled Polyethylene9 Product Morphology in Olefin Polymerization with Polymer Supported Metallocene Catalysts; 10 Review of Phillips Chromium Catalyst for Ethylene Polymerization; 11 Silica-Supported Silyl Chromate-Based Ethylene Polymerization Catalysts; 12 Ethylene Polymerization and α-Olefin Oligomerization Using Catalysts Derived from Phosphoranes and Ni(II) and Ni(0) Precursors; 13 Late Transition Metal-Catalyzed Co- and Terpolymerization of α-Olefins with Carbon Monoxide-Polyketones: Synthesis and Modification 14 Copper Catalysts for Olefin Polymerization15 Ring-Opening Metathesis Polymerizations and Acyclic Diene Metathesis Polymerizations with Homogeneous Ruthenium and Molybdenum Catalysts and Initiators; 16 Cobalt Ziegler-Natta Catalysts for Synthesis of Poly-cis-1,4-Butadiene; Appendix A Pyrophoricity of Metal Alkyls; Appendix B Rheological Terms for Polymerization Catalyst Chemists; Index |
| Record Nr. | UNINA-9910785239103321 |
| Hoboken, N.J., : Wiley, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of transition metal polymerization catalysts [[electronic resource] /] / edited by Ray Hoff, Robert T. Mathers
| Handbook of transition metal polymerization catalysts [[electronic resource] /] / edited by Ray Hoff, Robert T. Mathers |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2010 |
| Descrizione fisica | 1 online resource (599 p.) |
| Disciplina | 668.9/2 |
| Altri autori (Persone) |
HoffRaymond E
MathersRobert T |
| Soggetto topico |
Polymerization
Transition metal catalysts Metathesis (Chemistry) |
| ISBN |
1-282-81669-1
9786612816697 0-470-50443-9 0-470-50442-0 |
| Classificazione |
VH 7900
VH 9700 VK 8000 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
HANDBOOK OF TRANSITION METAL POLYMERIZATION CATALYSTS; CONTENTS; Introduction; About the Authors; 1 Commercially Available Metal Alkyls and Their Use in Polyolefin Catalysts; 2 Porous Silica in Transition Metal Polymerization Catalysts; 3 Computational Modeling of Polymerization Catalysts; 4 Scale-Up of Catalyst Recipes to Commercial Production; 5 Commercialization of Olefin Polymerization Catalysts: Model for Success; 6 Supported Magnesium/Titanium-Based Ziegler Catalysts for Production of Polyethylene; 7 Stereospecific α-Olefin Polymerization with Heterogeneous Catalysts
8 MgCl(2)-Supported TiCl(4) Catalysts for Production of Morphology-Controlled Polyethylene9 Product Morphology in Olefin Polymerization with Polymer Supported Metallocene Catalysts; 10 Review of Phillips Chromium Catalyst for Ethylene Polymerization; 11 Silica-Supported Silyl Chromate-Based Ethylene Polymerization Catalysts; 12 Ethylene Polymerization and α-Olefin Oligomerization Using Catalysts Derived from Phosphoranes and Ni(II) and Ni(0) Precursors; 13 Late Transition Metal-Catalyzed Co- and Terpolymerization of α-Olefins with Carbon Monoxide-Polyketones: Synthesis and Modification 14 Copper Catalysts for Olefin Polymerization15 Ring-Opening Metathesis Polymerizations and Acyclic Diene Metathesis Polymerizations with Homogeneous Ruthenium and Molybdenum Catalysts and Initiators; 16 Cobalt Ziegler-Natta Catalysts for Synthesis of Poly-cis-1,4-Butadiene; Appendix A Pyrophoricity of Metal Alkyls; Appendix B Rheological Terms for Polymerization Catalyst Chemists; Index |
| Record Nr. | UNINA-9910812131203321 |
| Hoboken, N.J., : Wiley, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||