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Dendrimers [Risorsa elettronica] : towards catalytic, material, and biomedical uses / Anne-Marie Caminade ... [et al.]
Dendrimers [Risorsa elettronica] : towards catalytic, material, and biomedical uses / Anne-Marie Caminade ... [et al.]
Pubbl/distr/stampa Chichester, West Sussex, U. K. : Wiley, , 2011
Disciplina 668.92
Soggetto non controllato Dendrimeri
ISBN 9781119976530
Formato Risorse elettroniche
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-990009793150403321
Chichester, West Sussex, U. K. : Wiley, , 2011
Risorse elettroniche
Lo trovi qui: Univ. Federico II
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Dendrimers : towards catalytic, material, and biomedical uses / / Anne-Marie Caminade ... [et al.]
Dendrimers : towards catalytic, material, and biomedical uses / / Anne-Marie Caminade ... [et al.]
Edizione [1st ed.]
Pubbl/distr/stampa Chichester, U.K. ; ; Hoboken, N.J., : Wiley, 2011
Descrizione fisica 1 online resource (558 p.) : ill
Disciplina 668.92
Altri autori (Persone) CaminadeAnne-Marie
Soggetto topico Dendrimers
ISBN 1-119-97757-6
1-283-24043-2
9786613240439
1-119-97653-7
1-119-97652-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction : what are dendrimers and dendrons? -- Syntheses of poly(propyleneimine) dendrimers (PPI) -- Synthesis of poly(amidoamine) dendrimers (PAMAM) -- Syntheses of poly(ether) dendrimers -- Syntheses of poly(ester) dendrimers -- Synthesis of poly(lysine) dendrimers -- Syntheses of silicon-containing dendrimers -- Syntheses of phosphorus-containing dendrimers -- Syntheses of carbon-based dendrimers -- Syntheses of dendrimers constituted of nitrogen heterocycles -- Syntheses by self-assembly -- Accelerated syntheses.
Record Nr. UNINA-9910139609103321
Chichester, U.K. ; ; Hoboken, N.J., : Wiley, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
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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
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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
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
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Hyperbranched Polydendrons : A New Macromolecular Architecture / / by Fiona L. Hatton
Hyperbranched Polydendrons : A New Macromolecular Architecture / / by Fiona L. Hatton
Autore Hatton Fiona L
Edizione [1st ed. 2015.]
Pubbl/distr/stampa Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015
Descrizione fisica 1 online resource (279 p.)
Disciplina 668.92
Collana Springer Theses, Recognizing Outstanding Ph.D. Research
Soggetto topico Medicinal chemistry
Polymers  
Nanochemistry
Medicinal Chemistry
Polymer Sciences
ISBN 3-319-18753-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Introduction -- Synthesis and characterisation of hyp-polydendron materials and subsequent anoparticle formation -- Mixing dendron and PEG initiators for the polymerisation of branched pHPMA and aqueous nanoparticle formation -- Mixing dendron and PEG initiators for the polymerisation of branched pHPMA and formation of sterically stabilised nanoparticles -- Hyp-Polydendrons; studies of nanoprecipitation behavior -- Conclusions and Future work -- Experimental.
Record Nr. UNINA-9910298614403321
Hatton Fiona L  
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015
Materiale a stampa
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Mathematical modelling for polymer processing : polymerization, crystallization, manufacturing / Vincenzo Capasso (editor)
Mathematical modelling for polymer processing : polymerization, crystallization, manufacturing / Vincenzo Capasso (editor)
Pubbl/distr/stampa Berlin [etc.] : Springer, 2003
Descrizione fisica XIV, 320 p. : ill. ; 24 cm
Disciplina 668.92
Collana Mathematics in industry
The european consortium for mathematics in industry
Soggetto topico Polimerizzazione - Modelli matematici
ISBN 3-540-4312-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-990001971520203316
Berlin [etc.] : Springer, 2003
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Molecularly Imprinted Polymers (MIPs) : challenges, uses and prospects / / Theodore Quinn, editor
Molecularly Imprinted Polymers (MIPs) : challenges, uses and prospects / / Theodore Quinn, editor
Pubbl/distr/stampa New York : , : Nova Publishers, , 2017
Descrizione fisica 1 online resource (209 pages) : illustrations, tables
Disciplina 668.92
Collana Polymer Science and Technology
Soggetto topico Molecular imprinting
Imprinted polymers
ISBN 1-63485-951-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910155229303321
New York : , : Nova Publishers, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Photoinitiators for polymer synthesis [[electronic resource] ] : scope, reactivity and efficiency / / Jean Pierre Fouassier and Jacques Lalevée
Photoinitiators for polymer synthesis [[electronic resource] ] : scope, reactivity and efficiency / / Jean Pierre Fouassier and Jacques Lalevée
Autore Fouassier Jean Pierre
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2012
Descrizione fisica 1 online resource (506 p.)
Disciplina 668.92
Altri autori (Persone) LalevéeJacques
Soggetto topico Polymerization
Radiation curing
Photochemistry - Industrial applications
ISBN 3-527-64826-7
3-527-64824-0
1-283-71443-4
3-527-64827-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Basic principles and applications of photopolymerization reactions -- pt. 2. Radical photoinitiating systems -- pt. 3. Nonradical photoinitiating systems -- pt. 4. Reactivity of the photoinitiating system.
Record Nr. UNINA-9910141412803321
Fouassier Jean Pierre  
Weinheim, Germany, : Wiley-VCH, 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Photoinitiators for polymer synthesis : scope, reactivity and efficiency / / Jean Pierre Fouassier and Jacques Lalevée
Photoinitiators for polymer synthesis : scope, reactivity and efficiency / / Jean Pierre Fouassier and Jacques Lalevée
Autore Fouassier Jean Pierre
Edizione [1st ed.]
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2012
Descrizione fisica 1 online resource (506 p.)
Disciplina 668.92
Altri autori (Persone) LalevéeJacques
Soggetto topico Polymerization
Radiation curing
Photochemistry - Industrial applications
ISBN 3-527-64826-7
3-527-64824-0
1-283-71443-4
3-527-64827-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Basic principles and applications of photopolymerization reactions -- pt. 2. Radical photoinitiating systems -- pt. 3. Nonradical photoinitiating systems -- pt. 4. Reactivity of the photoinitiating system.
Record Nr. UNINA-9910818042103321
Fouassier Jean Pierre  
Weinheim, Germany, : Wiley-VCH, 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Principles and applications of emulsion polymerization [[electronic resource] /] / Chorng-Shyan Chern
Principles and applications of emulsion polymerization [[electronic resource] /] / Chorng-Shyan Chern
Autore Chern Chorng-Shyan
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2008
Descrizione fisica 1 online resource (268 p.)
Disciplina 668.9
668.92
Soggetto topico Emulsion polymerization
Soggetto genere / forma Electronic books.
ISBN 1-281-75190-1
9786611751906
0-470-37794-1
0-470-37793-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto PRINCIPLES AND APPLICATIONS OF EMULSION POLYMERIZATION; CONTENTS; Preface; 1 Introduction; 1.1 Free Radical Polymerization; 1.1.1 Free Radical Polymerization Mechanisms; 1.1.2 Free Radical Polymerization Kinetics; 1.2 Emulsion Polymerization; 1.2.1 Conventional Emulsion Polymerization; 1.2.2 Emulsion Polymerization Processes; 1.2.3 Miniemulsion Polymerization; 1.2.4 Microemulsion Polymerization; 1.2.5 Inverse Emulsion Polymerization; 1.3 Colloidal Stability; 1.3.1 A Critical but Often Ignored Issue; 1.3.2 Electrostatic Interactions; 1.3.3 Steric Interactions; 1.3.4 Mechanical Stability
1.4 Some Performance Properties for Industrial Applications1.4.1 Rheology; 1.4.2 Film Formation; References; 2 Interfacial Phenomena; 2.1 Thermodynamic Consideration; 2.1.1 Emulsification of Oil in Water; 2.1.2 Interfaces; 2.1.3 Surfactant Molecules Adsorbed at an Interface; 2.2 Surfactants; 2.2.1 Critical Micelle Concentration (CMC); 2.2.2 Hydrophile-Lipophile Balance (HLB); 2.2.3 Solubility Parameter; 2.3 Colloidal Stability; 2.3.1 Van der Waals Forces; 2.3.2 Electrostatic Interactions; 2.3.3 Steric Interactions; 2.3.4 Kinetics of Flocculation; References; 3 Particle Nucleation Mechanisms
3.1 Micellar Nucleation3.1.1 Harkins-Smith-Ewart Theory; 3.1.2 Competitive Absorption of Free Radicals by Micelles and Particle Nuclei; 3.2 Homogeneous Nucleation; 3.2.1 Formation of Particle Nuclei in the Continuous Aqueous Phase; 3.2.2 Hansen-Ugelstad-Fitch-Tsai (HUFT) Model; 3.3 Coagulative Nucleation; 3.3.1 General Features of Coagulative Nucleation; 3.3.2 Coagulative Nucleation Model Development; 3.4 Mixed Mode of Particle Nucleation Mechanisms; 3.5 Surfactant-Free Emulsion Polymerization; 3.6 Experimental Work on Particle Nucleation; 3.6.1 A Dilemma about Particle Nucleation Mechanisms
3.6.2 Some Representative Experimental Data of Particle Nucleation3.6.3 Some Potential Techniques for Studying Particle Nucleation; 3.6.4 Effects of Surfactant Concentration on Particle Nucleation; 3.7 Nonionic and Mixed Surfactant Systems; 3.7.1 Nonionic Surfactant Systems; 3.7.2 Mixed Anionic and Nonionic Surfactant Systems; References; 4 Emulsion Polymerization Kinetics; 4.1 Emulsion Polymerization Kinetics; 4.1.1 Smith-Ewart Theory; 4.1.2 Pioneering Kinetic Models for Predicting Average Number of Free Radicals per Particle; 4.2 Absorption of Free Radicals by Latex Particles
4.2.1 Collision- and Diffusion-Controlled Models4.2.2 Propagation-Controlled Model; 4.2.3 Some Controversial Issues; 4.3 Desorption of Free Radicals Out of Latex Particles; 4.3.1 Desorption of Free Radicals in Emulsion Homopolymerization Systems; 4.3.2 Desorption of Free Radicals in Emulsion Copolymerization Systems; 4.3.3 Effect of Interfacial Properties on Desorption of Free Radicals; 4.4 Growth of Latex Particles; 4.4.1 Thermodynamic Consideration; 4.4.2 Concentrations of Comonomers in Emulsion Copolymerization Systems; 4.4.3 Competitive Growth of Latex Particles
4.5 Polymer Molecular Weight
Record Nr. UNINA-9910144135703321
Chern Chorng-Shyan  
Hoboken, N.J., : Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
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