This book, cohesively written by an expert author with supreme breadth and depth of perspective on polyurethanes, provides a comprehensive overview of all aspects of the science and technology on one of the most commonly produced plastics. _ Covers the applications, manufacture, and markets for polyurethanes, and discusses analytical methods, reaction mechanisms, morphology, and synthetic routes _ Provides an up-to-date view of the current markets and trend analysis based on patent activity and updates chapters to include new research _ Includes two new chapters on PU recycling and PU hybrids, covering the opportunities and challenges in both…mehr
This book, cohesively written by an expert author with supreme breadth and depth of perspective on polyurethanes, provides a comprehensive overview of all aspects of the science and technology on one of the most commonly produced plastics.
_ Covers the applications, manufacture, and markets for polyurethanes, and discusses analytical methods, reaction mechanisms, morphology, and synthetic routes _ Provides an up-to-date view of the current markets and trend analysis based on patent activity and updates chapters to include new research _ Includes two new chapters on PU recycling and PU hybrids, covering the opportunities and challenges in bothHinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Produktdetails
Produktdetails
Wiley Series on Plastics Engineering and Technology
MARK F. SONNENSCHEIN, PHD, is research fellow with The Dow Chemical Company. He is inventor of Dow's LESATM (Low Surface Energy Adhesive), Voranol VorativTM polyurethane polyol, HermesTM thermoplastic polyurethane elastomer, RenuvaTM seed oil derived polyol, Voranol 223-060LMTM polyol, and numerous other technologies.
Inhaltsangabe
Preface
Acknowledgments
Chapter 1 Introduction
Chapter 2 Polyurethane Building Blocks
2.1 Polyols
2.11 Polyether polyols
2.111 Building blocks
2.112 Polymerization of alkoxides to polyethers
2.12 Polyester polyols
2.121 Polyester polyol building blocks
2.122 Preparation of polyester polyols
2.123 Aliphatic polyester polyols
2.124 Aromatic Polyester Polyols
2. 13 Other Polyols
2.131 Polycarbonate Polyols
2.1311. Preparation of polycarbonate polyols
2. 132 Polyacrylate polyols
2.1321 Preparation of acrylic polyols
2.14. Filled polyols
2.141 Copolymer polyols
2.142 PHD Polyols
2.143 PIPA polyols
2.15 Seed-oil derived polyols
2.151 Preparation of seed oil derived polyols
2.1511 Epoxidation and ring opening
2.1512 Ozonolysis
2.1513 Hydroformylation and reduction
2.1514 Metathesis
2.16 Prepolymers
2.2 Isocyanates
2.21 TDI
2.211 Conventional Production of TDI
2.212 Non-phosgene routes to TDI
2.2121 Thermolysis of Carbamic acid, N,N'-(4-methyl-1,3-phenylene)bis-, C,C'-dimethyl ester made from the reaction of toluene diamine with methyl carbonate
2.2122 Thermolysis of Carbamic acid, N,N'-(4-methyl-1,3-phenylene)bis-, C,C'-dimethyl ester made from the reductive carbonylation of dinitrotoluene.
2.2123 Isocyanates by thermal decomposition of acyl azides - The Curtius rearrangement
2.2121 Thermolysis of Carbamic acid, N,N'-(4-methyl-1,3-phenylene)bis-, C,C'-dimethyl ester made from the reaction of toluene diamine with methyl carbonate
2.2122 Thermolysis of Carbamic acid, N,N'-(4-methyl-1,3-phenylene)bis-, C,C'-dimethyl ester made from the reductive carbonylation of dinitrotoluene.
2.2123 Isocyanates by thermal decomposition of acyl azides - The Curtius rearrangement
