LEADER 05111nam 2200601Ia 450 001 9910877294403321 005 20200520144314.0 010 $a1-281-78800-7 010 $a9786611788001 010 $a0-470-38599-5 010 $a0-470-38598-7 035 $a(CKB)1000000000540928 035 $a(EBL)469334 035 $a(OCoLC)263428470 035 $a(SSID)ssj0000099134 035 $a(PQKBManifestationID)11124795 035 $a(PQKBTitleCode)TC0000099134 035 $a(PQKBWorkID)10013157 035 $a(PQKB)11564911 035 $a(MiAaPQ)EBC469334 035 $a(EXLCZ)991000000000540928 100 $a20080229d2008 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aAdvances in polymer chemistry and methods reported in recent U.S. patents /$fThomas F. DeRosa 210 $aHoboken, NJ $cWiley$dc2008 215 $a1 online resource (757 p.) 300 $aIncludes index. 311 $a0-470-31286-6 327 $aADVANCES IN POLYMER CHEMISTRY AND METHODS REPORTED IN RECENT US PATENTS; CONTENTS; Preface; I. ADDITIVES; Controlled Radical Acrylic Copolymer Thickeners; Polymer-Filler Coupling Additives; II. ADHESIVES; (Meth)acrylate Block Copolymer Pressure Sensitive Adhesives; Absorbable ?-Cyanoacrylate Compositions; Use of Polybenzoxazoles (PBOS) for Adhesion; III. BIOACTIVE; A. Bioabsorbables; Segmented Urea and Siloxane Copolymers and Their Preparation Methods; Functionalized Polymers for Medical Applications; Degradable Polyacetal Polymers; Lactone Bearing Absorbable Polymers; B. Contact Lenses 327 $aLow Polydispersity Poly-HEMA CompositionsC. Drug Delivery; Amphiphilic Block Copolymers and Nanoparticles Comprising the Same; Heterofunctional Copolymers of Glycerol and Polyethylene Glycol, Their Conjugates and Compositions; Polyalkylene Glycol Acid Additives; Thermosensitive Biodegradable Copolymer; Polyamide Graft Copolymers; Bioerodible Poly(Ortho Esters) from Dioxane-Based Di(Ketene Acetals) and Block Copolymers Containing Them; Water-Soluble Polymer Alkanals; Biodegradable Aliphatic Polyester Grafted with Poly(Ethylene Glycol) Having Reactive Groups and Preparation Method Thereof 327 $aCoumarin End-Capped Absorbable PolymersBlock Copolymers for Multifunctional Self-assembled Systems; Methods of Making Functional Biodegradable Polymers; Monofunctional Polyethylene Glycol Aldehydes; IV. COATINGS; A. Anionic; Glycopolymers and Free Radical Polymerization Methods; B. Aqueous; Method of Making Novel Water-Soluble and Self-doped Polyaniline Graft Copolymers; Oxyfluorination; Aqueous Dispersions of Crystalline Polymers and Uses; C. Fluorine; Multifunctional (Meth)Acrylate Compound, Photocurable Resin Composition and Article; D. Hydrophilic 327 $aPolyoxyalkylene Phosphonates and Improved Process for Their SynthesisE. Hydrophobic; Polymers and Polymer Coatings; Photochemical Crosslinkers for Polymer Coatings and Substrate Tie-Layer; Use of Poly(Dimethyl Ketone) to Manufacture Articles in Direct Contact with a Humid or Aqueous Medium; F. Thermally Stable; Polyaryleneetherketone Phosphine Oxide Compositions Incorporating Cycloaliphatic Units for Use as Polymeric Binders in Thermal Control Coatings and Method for Synthesizing Same; G. Vapor Deposition of Polymers; Functionalization of Porous Materials by Vacuum Deposition of Polymers 327 $aH. Succinic Anhydride DerivativesLight Absorbent Agent Polymer for Organic Anti-reflective Coating and Preparation Method and Organic Anti-reflective Coating Composition Comprising the Same; V. COSMETICS; Water-Soluble or Water-Dispersible Graft Polymers, Their Preparation and Use; VI. DENTAL; A. Cement; (Meth)Acrylate-Substituted Iminooxidiazine Dione Derivatives; B. Dental Composites; (Meth)Acrylic Ester Compound and Use Thereof; VII. ELECTROACTIVE; A. Charge Transport Materials; Hole Transport Polymers and Devices Made with Such Polymers; Acrylic Polymer and Charge Transport Material 327 $aB. Dielectric Materials 330 $aThe objective of this book is to convey to academic and industrial researchers and students advances in synthetic and characterization methods in 9 selected areas of polymer chemistry reported in 2007-2008 US Patents. It reviews the impact of newer bulk anionic, cationic, and free radical polymerization methods within selected industrial applications. Bulk and surface crosslinking agents using selected bi- and tri-functional reagents, photochemical methods, or free radical agents are also reviewed. Finally, there is a separate section on cationic and cationic ring opening polymerization reacti 606 $aPolymers 606 $aPolymerization 615 0$aPolymers. 615 0$aPolymerization. 676 $a668.9 686 $aUV 1000$2rvk 700 $aDeRosa$b Thomas F$0863953 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910877294403321 996 $aAdvances in polymer chemistry and methods reported in recent U.S. patents$94191900 997 $aUNINA