03121nam 2200601Ia 450 991045338730332120200520144314.01-281-92801-19786611928018981-277-527-7(CKB)1000000000553155(EBL)1214912(SSID)ssj0000301557(PQKBManifestationID)12071799(PQKBTitleCode)TC0000301557(PQKBWorkID)10263783(PQKB)10514980(MiAaPQ)EBC1214912(WSP)00000831 (Au-PeEL)EBL1214912(CaPaEBR)ebr10698960(CaONFJC)MIL192801(OCoLC)820942538(EXLCZ)99100000000055315520050329d2005 uy 0engur|n|---|||||txtccrLecture notes on applied reservoir simulation[electronic resource] /Leonard F. KoederitzHackensack, NJ World Scientific Pub.c20051 online resource (214 p.)Description based upon print version of record.981-256-198-6 Includes bibliographical references (p. 160) and index.Preface; CONTENTS; Chapter 1 Introduction; 1.1 Types of Models; 1.2 Data Requirements; Chapter 2 Theoretical Development; 2.1 Flow Equations; 2.2 Types of Simulators; 2.3 Solution Techniques; Chapter 3 PVT Data; Chapter 4 Relative Permeability and Capillary Pressure Data; Chapter 5 Transmissibilities; Chapter 6 Gridding Considerations; Chapter 7 Well Packages; Chapter 8 Field Studies; Chapter 9 Other Types of Models; 9.1 Radial Simulators; 9.2 Dual Porosity Simulators; Chapter 10 Odds and Ends; 10.1 Advantages of Reservoir Simulation; 10.2 Disadvantages of Reservoir Simulation; ReferencesSimulation and Reservoir Property BooksAppendix A; Fluid and Formation Correlations; Solutions to Problems; IndexReservoir simulation, or modeling, is one of the most powerful techniques currently available to the reservoir engineer. The author, Prof Leonard F Koederitz, (Distinguished Teaching Professor Emeritus at the University of Missouri-Rolla) is a highly notable author and teacher, with many teaching awards. This book has been developed over his twenty years in teaching to undergraduate petroleum engineering students, with the knowledge that they would in all likelihood be model-users, not developers.Most other books on reservoir simulation deal with simulation theory and development. For this booOil fieldsComputer simulationPetroleumGeologyMathematical modelsElectronic books.Oil fieldsComputer simulation.PetroleumGeologyMathematical models.622/.3382/0113Koederitz Leonard940250MiAaPQMiAaPQMiAaPQBOOK9910453387303321Lecture notes on applied reservoir simulation2120088UNINA05459nam 2200673Ia 450 991013951130332120170810194931.01-282-47206-297866124720600-470-74886-90-470-74885-0(CKB)2550000000002112(EBL)477884(OCoLC)463438682(SSID)ssj0000335873(PQKBManifestationID)11273401(PQKBTitleCode)TC0000335873(PQKBWorkID)10278286(PQKB)10546062(MiAaPQ)EBC477884(PPN)143478532(EXLCZ)99255000000000211220090428d2009 uy 0engur|n|---|||||txtccrClick chemistry for biotechnology and materials science[electronic resource] /edited by Joerg LahannChichester, West Sussex Wiley20091 online resource (433 p.)Description based upon print version of record.0-470-69970-1 Includes bibliographical references and index.Click Chemistry for Biotechnologyand Materials Science; Contents; Preface; List of Contributors; Acknowledgments; 1 Click Chemistry: A Universal Ligation Strategy for Biotechnology and Materials Science; 1.1 Introduction; 1.2 Selected Examples of Click Reactions in Materials Science and Biotechnology; 1.3 Potential Limitations of Click Chemistry; 1.4 Conclusions; References; 2 Common Synthons for Click Chemistry in Biotechnology; 2.1 Introduction - Click Chemistry; 2.2 Peptides and Derivatives; 2.3 Peptoids; 2.4 Peptidic Dendrimers; 2.5 Oligonucleotides; 2.6 Carbohydrates; 2.7 ConclusionReferences3 Copper-free Click Chemistry; 3.1 Introduction; 3.2 Bio-orthogonal Ligations; 3.2.1 Condensations of Ketones and Aldehydes with Heteroatom-bound Amines; 3.2.2 Staudinger Ligation of Phosphines and Azides; 3.2.3 Copper-free Azide-Alkyne Cycloadditions; 3.2.4 Bioorthogonal Ligations of Alkenes; 3.3 Applications of Copper-free Click Chemistries; 3.3.1 Activity-based Profiling of Enzymes; 3.3.2 Site-specific Labeling of Proteins; 3.3.3 Metabolic Labeling of Glycans; 3.3.4 Metabolic Targeting of Other Biomolecules with Chemical Reporters; 3.4 Summary and Outlook; References4 Protein and Peptide Conjugation to Polymers and Surfaces Using Oxime Chemistry4.1 Introduction; 4.2 Protein/Peptide-Polymer Conjugates; 4.3 Immobilization of Proteins and Peptides on Surfaces; 4.4 Conclusions; References; 5 The Role of Click Chemistry in Polymer Synthesis; 5.1 Introduction; 5.2 Polymerization via CuAAC; 5.3 Post-polymerization Modification via Click Chemistry; 5.4 Polymer-Biomacromolecule Conjugation; 5.5 Functional Nanomaterials; 5.6 Summary and Outlook; References; 6 Blocks, Stars and Combs: Complex Macromolecular Architecture Polymers via Click Chemistry6.1 Introduction6.2 Block Copolymers; 6.2.1 Preparing Polymers for Click Conjugations; 6.2.2 The Click Reaction: Methodologies and Isolation; 6.2.3 Polymer Characterization; 6.3 Star Polymers; 6.3.1 Star polymers An; 6.3.2 Dentritic Star Polymers; 6.4 Graft Copolymers; 6.4.1 'Grafting-to' Azide Main Chains; 6.4.2 'Grafting-to' Alkyne Main Chains; 6.4.3 Non-CuAAC Routes; 6.5 Concluding Remarks; References; 7 Click Chemistry on Supramolecular Materials; 7.1 Introduction; 7.2 Click Reactions on Rotaxanes, Cyclodextrines and Macrocycles; 7.2.1 Click with Rotaxanes; 7.2.2 Click on Cyclodextrines7.2.3 Click on Macrocycles7.3 Click Reactions on DNA; 7.4 Click Reactions on Supramolecular Polymers; 7.5 Click Reactions on Membranes; 7.6 Click Reactions on Dendrimers; 7.7 Click Reactions on Gels and Networks; 7.8 Click Reactions on Self-assembled Monolayers; References; 8 Dendrimer Synthesis and Functionalization by Click Chemistry for Biomedical Applications; 8.1 Introduction; 8.2 Dendrimer Synthesis; 8.2.1 Divergent Synthesis; 8.2.2 Convergent Synthesis; 8.3 Dendrimer Functionalization; 8.4 Conclusions and Future Directions; References9 Reversible Diels-Alder Cycloaddition for the Design of Multifunctional Network PolymersMimicking natural biochemical processes, click chemistry is a modular approach to organic synthesis, joining together small chemical units quickly, efficiently and predictably. In contrast to complex traditional synthesis, click reactions offer high selectivity and yields, near-perfect reliability and exceptional tolerance towards a wide range of functional groups and reaction conditions. These 'spring loaded' reactions are achieved by using a high thermodynamic driving force, and are attracting tremendous attention throughout the chemical community. Originally introduced with the focus on druBiotechnologyMaterials scienceCombinatorial chemistryMacromoleculesSynthesisBiotechnology.Materials science.Combinatorial chemistry.MacromoleculesSynthesis.620.11660.6Lahann Joerg854334MiAaPQMiAaPQMiAaPQBOOK9910139511303321Click chemistry for biotechnology and materials science1907766UNINA