Offering a unique perspective summarizing research on this timely important topic around the globe, this book provides comprehensive coverage of how molecular biomass can be transformed into sustainable polymers. It critically discusses and compares a few classes of biomass – oxygen–rich, hydrocarbon–rich, hydrocarbon and non–hydrocarbon (including carbon dioxide) as well as natural polymers – and equally includes products that are already commercialized. A must–have for both newcomers to the field as well as established researchers in both academia and industry. INDICE: List of Contributors xi .1 Introduction 1Mitra S. Ganewatta, Chuanbing Tang, and Chang Y. Ryu .1.1 Introduction 1 .1.2 Sustainable Polymers 2 .1.3 Biomass Resources for Sustainable Polymers 4 .1.4 Conclusions 8 .References 8 .2 Polyhydroxyalkanoates: Sustainability, Production, and Industrialization 11Ying Wang and Guo–Qiang Chen .2.1 Introduction 11 .2.2 PHA Diversity and Properties 14 .2.3 PHA Production from Biomass 16 .2.4 PHA Application and Industrialization 26 .2.5 Conclusion 28 .Acknowledgment 28 .References 28 .3 Polylactide: Fabrication of Long Chain Branched Polylactides and Their Properties and Applications 35Zhigang Wang and Huagao Fang .3.1 Introduction 35 .3.2 Fabrication of LCB PLAs 36 .3.3 Structural Characterization on LCB PLAs 38 .3.4 The Rheological Properties of LCB PLAs 43 .3.5 Crystallization Kinetics of LCB PLAs 46 .3.6 Applications of LCB PLAs 48 .3.7 Conclusions 51 .Acknowledgments 51 .References 51 .4 Sustainable Vinyl Polymers via Controlled Polymerization of Terpenes 55Masami Kamigaito and Kotaro Satoh .4.1 Introduction 55 .4.2 –Pinene 57 .4.3 –Pinene 63 .4.4 Limonene 65 .4.5 –Myrcene, –Ocimene, and Alloocimene 69 .4.6 Other Terpene or Terpenoid Monomers 76 .4.7 Conclusion 80 .Abbreviations 80 .References 81 .5 Use of Rosin and Turpentine as Feedstocks for the Preparation of Polyurethane Polymers 91Meng Zhang, Yonghong Zhou, and Jinwen Zhang .5.1 Introduction 91 .5.2 Rosin Based Polyurethane Foams 92 .5.3 Rosin–Based Polyurethane Elastomers 95 .5.4 Terpene–Based Polyurethanes 95 .5.5 Terpene–Based Waterborne Polyurethanes 97 .5.6 Rosin–Based Shape Memory Polyurethanes 99 .5.7 Conclusions 100 .References 101 .6 Rosin–Derived Monomers and Their Progress in Polymer Application 103Jifu Wang, Shaofeng Liu, Juan Yu, Chuanwei Lu, Chunpeng Wang, and Fuxiang Chu .6.1 Introduction 103 .6.2 Rosin Chemical Composition 104 .6.3 Rosin Derived Monomers for Main–Chain Polymers 105 .6.4 Rosin–Derived Monomers for Side–Chain Polymers 112 .6.5 Rosin–Derived Monomers for Three–Dimensional Rosin–Based Polymer 131 .6.6 Outlook and Conclusions 140 .Acknowledgments 141 .References 141 .7 Industrial Applications of Pine–Chemical–Based Materials 151Lien Phun, David Snead, Phillip Hurd, and Feng Jing .7.1 Pine Chemicals Introduction 151 .7.2 Crude Tall Oil 151 .7.3 Terpenes 153 .7.4 Tall Oil Fatty Acid 159 .7.5 Rosin 167 .7.6 Miscellaneous Products 173 .References 178 .8 Preparation and Applications of Polymers with Pendant Fatty Chains from Plant Oils 181Liang Yuan, Zhongkai Wang, Nathan M. Trenor, and Chuanbing Tang .8.1 Introduction 181 .8.2 (Meth)acrylate Monomers Preparation and Polymerization 182 .8.3 Norbornene Monomers and Polymers for Ring Opening Metathesis Polymerization (ROMP) 194 .8.4 2–Oxazoline Monomers for Living Cationic Ring Opening Polymerization 195 .8.5 Vinyl Ether Monomers for Cationic Polymerization 200 .8.6 Conclusions and Outlook 203 .References 204 .9 Structure Property Relationships of Epoxy Thermoset Networks from Photoinitiated Cationic Polymerization of Epoxidized Vegetable Oils 209Zheqin Yang, Jananee Narayanan, Matthew Ravalli, Brittany T. Rupp, and Chang Y. Ryu .9.1 Introduction 209 .9.2 Photoinitiated Cationic Polymerization of Epoxidized Vegetable Oils 213 .9.3 Conclusions 224 .Acknowledgment 225 .References 225 .10 Biopolymers from Sugarcane and Soybean Lignocellulosic Biomass 227Delia R. Tapia–Blácido, Bianca C. Maniglia, and Milena Martelli–Tosi .10.1 Introduction 227 .10.2 Lignocellulosic Biomass Composition and Pretreatment 229 .10.3 Lignocellulosic Biomass from Soybean 233 .10.4 Production of Polymers from Soybean Biomass 234 .10.5 Lignocellulosic Biomass from Sugarcane 242 .10.6 Production of Polymers from Sugarcane Bagasse 242 .10.7 Conclusion and Future Outlook 246 .Acknowledgments 247 .References 247 .11 Modification of Wheat Gluten–Based Polymer Materials by Molecular Biomass 255Xiaoqing Zhang .11.1 Introduction 255 .11.2 Modification of Wheat Gluten Materials by Molecular Biomass 257 .11.3 Biodegradation of Wheat Gluten Materials Modified by Biomass 269 .11.4 Biomass Fillers for WG Biocomposites 271 .11.5 Conclusion and Future Perspectives of WG–Based Materials 272 .References 273 .12 Copolymerization of C1 Building Blocks with Epoxides 279Ying–Ying Zhang and Xing–Hong Zhang .12.1 Introduction 279 .12.2 CO2/Epoxide Copolymerization 280 .12.3 CS2/Epoxide Copolymerization 295 .12.4 COS/Epoxide Copolymerization 299 .12.5 Properties of C1–Based Polymers 304 .12.6 Conclusions and Outlook 307 .References 307 .13 Double–Metal Cyanide Catalyst Design in CO2/Epoxide Copolymerization 315Joby Sebastian and Darbha Srinivas .13.1 Introduction 315 .13.2 Polycarbonates and Their Synthesis Methods 317 .13.3 Copolymerization of CO2 and Epoxides 318 .13.4 Double–Metal Cyanides and Their Structural Variation 319 .13.5 Methods of DMC Synthesis 322 .13.6 Factors Influencing Catalytic Activity of DMCs 323 .13.7 Role of Co–catalyst on the Activity of DMC Catalysts 332 .13.8 Copolymerization in the Presence of Hybrid DMC Catalysts 334 .13.9 Copolymerization with Nano–lamellar DMC Catalysts 335 .13.10 Effect of Crystallinity and Crystal Structure of DMC on Copolymerization 337 .13.11 Effect of Method of Preparation of DMC Catalysts on Their Structure and Copolymerization Activity 337 .13.12 Reaction Mechanism of Copolymerization 340 .13.13 Conclusions 342 .References 343 .Index 347
- ISBN: 978-3-527-34016-3
- Editorial: Wiley VCH
- Encuadernacion: Cartoné
- Páginas: 376
- Fecha Publicación: 05/04/2017
- Nº Volúmenes: 1
- Idioma: Inglés