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Cellulose-Based Graft Copolymers Structure and Chemistry

Langue : Anglais

Coordonnateur : Thakur Vijay Kumar

Couverture de l’ouvrage Cellulose-Based Graft Copolymers

Cellulose-Based Graft Copolymers: Structure and Chemistry discusses the synthesis, characterization, and properties of multifunctional cellulose-based graft copolymers. Presenting the contributions of accomplished experts in the field of natural cellulosic polymers, this authoritative text:

  • Offers an overview of cutting-edge technical accomplishments in natural cellulose-based graft polymers
  • Addresses a separate biomaterial in each chapter, exploring composition as well as graft copolymerization chemistry
  • Covers fundamentals and applications including toxic ion removal, biomedical engineering, biofuels, micro/nano composites, papermaking, building materials, and defense

Cellulose-Based Graft Copolymers: Structure and Chemistry tackles several critical issues and provides suggestions for future work, supplying deeper insight into the state of the art of advanced cellulose-based graft copolymers.

Cellulose-Based Graft Copolymers: An Overview. Grafting on Cellulosics: Progress toward Purpose. Preparation of Functional Polymer-Grafted Cellulose through Azide Alkyne Cycloaddition or C-C Cross-Coupling. Graft Copolymerization of Cellulose and Cellulose Derivatives. Cellulose Graft Copolymerization by Gamma and Electron Beam Irradiation. Advances in Cellulose-Based Graft Copolymers Prepared via Controlled Radical Polymerization Methods: A Comprehensive Review. UV-Grafting: A Powerful Tool for Cellulose Surface Modification. Graft Copolymerization of Vinyl Monomers onto Cellulosic Cannabis indica Fibers. Advances, Development, and Characterization of Cellulose Graft Copolymers. Modification of Cellulose-Based Fibers by the Graft Copolymerization Method. Modification of Jute Fibers by Radiation-Induced Graft Copolymerization and Their Applications. Chemically Modified Cotton Fibers for Antimicrobial Applications. Cellulose-Based Graft Copolymer for Toxic Ion and Organic Persistent Pollutants Removal. Use of Oxidized Regenerated Cellulose in Controlling Bleeding during Neurosurgical Procedures. Hydroxypropyl Methyl Cellulose Grafted with Poly(Acrylamide): Application as Novel Polymeric Material as Flocculant as well as Adsorbent. Preparation of Graft Copolymers of Cellulose Derivatives and Their Use in Recovery Processes. Grafting of Cellulose-Based Materials: Techniques, Factors, and Applications of the Grafted Products. Preparation, Self-Assembly, and Application of Amphiphilic Cellulose-Based Graft Copolymers. Hydroxypropyl Cellulose-Based Graft Copolymers: Structure, Properties, and Application. Intelligent Responsive Copolymers Based on Cellulose: Structure, Properties, and Applications. Synthesis and Applications of Grafted Carboxymethyl Cellulose: A Review. Surface Grafting of Cellulose Nanowhisker. Nanocellulose Preparation, Surface Chemical Modification, and Its Application. Synthesis and Characterization of Sulfonyl-Terminated Polymer-Grafted Magnetic Nanocellulose and Its Application as a pH-Responsive Antibiotic Drug Carrier for the Controlled Delivery of Ciprofloxacin. Grafting of Cellulose and Cellulose Derivatives by CuAAC Click Chemistry.

Vijay Kumar Thakur is currently a staff scientist in the School of Mechanical and Materials Engineering at Washington State University, Pullman, USA. His former appointments include a research scientist in Temasek Laboratories at Nanyang Technological University, Singapore, and a visiting research fellow in the Department of Chemical and Materials Engineering at Lunghwa University of Science and Technology, Taiwan. He completed his postdoctorate in materials science at Iowa State University, Ames, USA, and his Ph.D in polymer science at the National Institute of Technology, Hamirpur, India. In addition to being widely published, Dr. Thakur is an editorial board member of numerous international journals, guest editor of the International Journal of Polymer Science and Journal of Chemistry, and member of several scientific bodies around the world.

Date de parution :

17.8x25.4 cm

Disponible chez l'éditeur (délai d'approvisionnement : 15 jours).

305,19 €

Ajouter au panier

Date de parution :

17.8x25.4 cm

Disponible chez l'éditeur (délai d'approvisionnement : 14 jours).

120,12 €

Ajouter au panier

Mots-clés :

Graft Copolymers; Cellulose Graft Copolymerization; Amphiphilic Cellulose-Based Graft Copolymers; Cellulose Based Graft Copolymers; Antimicrobial Chemically Modified Cotton Fibers; Ceric Ammonium Nitrate; Azide Alkyne Cycloaddition; Raft Polymerization; C-C Cross-Coupling; GP; Cellulose Derivatives; Cellulose Graft Copolymers; Graft Chains; Cellulose Grafting by CuAAC Click Chemistry; CNW; Cellulose Nanowhisker Surface Grafting; Cellulosic Bers; Cellulose Surface Modification; Natural Bers; Cellulose-Based Fiber Modification; Cellulose Backbone; Cellulose-Based Graft Copolymers; Cellulose Graft; Cellulose-Based Intelligent Responsive Copolymers; Click Chemistry; Cellulose-Based Material Grafting; ROP; Cellulosic Cannabis indica Fibers; Cotton Bers; Controlled Delivery of Ciprofloxacin; Radiation Induced Graft Copolymerization; Controlled Radical Polymerization Methods; Binary Monomer Mixture; Functional Polymer-Grafted Cellulose Preparation; Amp; Gamma and Electron Beam Irradiation; Polysaccharide Backbone; Graft Copolymerization Methods; UV Curable Coating; Grafted Carboxymethyl Cellulose; Graft Yield; Grafting on Cellulosics; Free Radical Sites; Hydroxypropyl Cellulose-Based Graft Copolymers; Adsorbent Dosage; Hydroxypropyl Methyl Cellulose Graft; GMA; Jute Fiber Modification; Multifunctional Cellulose-Based Graft Copolymers; Nanocellulose Surface Chemical Modification; Natural Cellulosic Polymers; Neurosurgical Controlled Bleeding; Organic Persistent Pollutants Removal; Oxidized Regenerated Cellulose Use; Poly(Acrylamides); Radiation-Induced Graft Copolymerization; Sulfonyl-Terminated Polymer-Grafted Magnetic Nanocellulose; Toxic Ion Removal; UV-Grafting; Vinyl Monomer Graft Copolymerization; pH-Responsive Antibiotic Drug Carriers