Anmerkung: Intro -- Contents -- 1 Biomass-Derived Polyurethanes for Sustainable Future -- Abstract -- 1 Introduction -- 1.1 Chemicals for Preparation of Polyurethanes -- 1.2 Importance of Green Chemicals and Synthesis Methods -- 1.3 Characteristics of Biomaterials for Polyurethanes -- 2 Bio-Oils as a Renewable Resource for Polyurethanes -- 2.1 Epoxidation and Ring-Opening Reactions -- 2.2 Hydroformation and Hydrogenation Reactions -- 2.3 Ozonolysis -- 2.4 Thiol-Ene Reaction -- 2.5 Transesterification Reaction -- 3 Terpenes as Green Starting Chemicals for Polyurethanes -- 4 Lignin for Green Polymers -- 5 Conclusion -- References -- 2 Mechanochemistry: A Power Tool for Green Synthesis -- Abstract -- 1 Introduction -- 2 History of Mechanochemistry -- 3 Principles of Mechanochemistry -- 3.1 Mechanisms and Kinetics of Mechanochemistry -- 3.2 Effects of Reaction Parameters -- 4 Mechanochemical Synthesis of Materials -- 4.1 Mechanochemical Synthesis of Co-crystals -- 4.2 Mechanochemistry in Inorganic Synthesis -- 4.3 Mechanochemistry in Organic Synthesis -- 4.4 Mechanochemistry in Metal-Organic Frameworks (MOFs) -- 4.5 Mechanochemistry in Porous Organic Materials (POMs) -- 4.6 Mechanochemical Synthesis of Polymers -- 5 Conclusions -- References -- 3 Future Trends in Green Synthesis -- Abstract -- 1 Introduction -- 2 Green Chemistry Metrics -- 2.1 Atom Economy (AE) -- 2.2 Environmental Factor (E Factor) -- 2.3 Process Mass Intensity (PMI) -- 2.4 Reaction Mass Efficiency (RME) -- 3 Application of Green Concept in Synthesis -- 3.1 Solvent-Based Organic Synthesis -- 3.2 Aqueous Medium -- 3.2.1 Micellar Media -- 3.2.2 Different Non-Aqueous Media -- Ionic Liquids -- Fluorous Media -- Supercritical Fluid -- Solvent-Free Synthesis -- 4 Future Trends -- References -- 4 Plant-Mediated Green Synthesis of Nanoparticles -- Abstract -- 1 Introduction. , 2 Methods for Metallic Nanoparticle Biosynthesis -- 3 Green Biosynthesis of Metallic NPs -- 3.1 Gold Nanoparticles -- 3.2 Platinum Nanoparticles -- 3.3 Silver Nanoparticles -- 3.4 Zinc Oxide Nanoparticles -- 3.5 Titanium Dioxide Nanoparticles -- 4 Different Parts Used for the Synthesis of Metallic Nanoparticles -- 4.1 Fruit -- 4.2 Stem -- 4.3 Seeds -- 4.4 Flowers -- 4.5 Leaves -- 5 Conclusions -- References -- 5 Green Synthesis of Hierarchically Structured Metal and Metal Oxide Nanomaterials -- Abstract -- 1 Introduction -- 2 Advantages of Green Synthesis Methods -- 3 Green Synthesis Methods for Hierarchically Structured Metal and Metal Oxide Nanomaterials -- 3.1 Biological Methods -- 3.1.1 Using Microorganism -- Microorganisms as Reactant -- Microorganism as Template -- 3.1.2 Using Plant -- Plant as Reactant -- Plant as Template -- 3.1.3 Using Other Green Templates -- 3.2 Physical and Chemical Methods -- 3.2.1 Green Techniques -- 3.2.2 Green Reagents -- 3.2.3 Green Solvents -- 4 Growth Mechanism of Metal and Metal Oxide HSNs -- 4.1 Biological Method -- 4.1.1 Biomolecules as Reagents -- 4.1.2 Biomolecules as Templates -- 4.2 Physical and Chemical Methods -- 5 Applications of Hierarchically Structured Metal and Metal Oxide Nanomaterials -- 5.1 Biomedical Application -- 5.2 Environmental Remediation -- 5.2.1 Wastewater Treatment -- 5.2.2 Energy Storage -- 5.2.3 Sensing -- 6 Present Challenges and Future Prospect -- Acknowledgements -- References -- 6 Bioprivileged Molecules -- Abstract -- 1 Introduction -- 2 Four Carbon 1,4-Diacids -- 2.1 Succinic Acid -- 2.2 Fumaric Acid -- 2.3 Malic Acid -- 3 Furan 2,5-Dicarboxylic Acid (FDCA) -- 4 3-Hydroxypropionic Acid (3-HPA) -- 5 Glucaric Acid -- 6 Glycerol -- 7 Aspartic Acid -- 8 Itaconic Acid -- 9 3-Hydroxybutyrolactone -- 10 Sorbitol -- 11 Xylitol -- 12 Glutamic Acid -- 13 Levulinic Acid. , 14 Emerging Molecules -- 15 Conclusion -- References -- 7 Membrane Reactors for Green Synthesis -- Abstract -- 1 Introduction -- 2 Chemical Reaction Enzymatic MR Using Supercritical CO2-IL -- 2.1 Ionic Liquid Media Effect on Free CLAB -- 2.2 Butyl Propionate Synthesis Using Active Membranes SC-CO2 and SC-CO2/IL -- 2.3 Butyl Propionate Synthesis Using Active Membranes in Hexane/IL -- 3 Mixed Ionic Electronic MR -- 3.1 Methane Flow Rate and Concentration Effects on Side II of Membrane -- 3.2 Steam Flow Effect on Side I of Membrane -- 3.3 Temperature Effect -- 4 Green Synthesis of Methanol in a Membrane Reactor -- 5 Green Fuel Energy -- 5.1 Green H2 Energy -- 5.2 Biofuel Energy -- 5.3 Green Fuel Additive -- 6 Biocatalyst Membrane Reactors -- 7 Photocatalytic Membrane Reactors -- 8 Conclusions -- References -- 8 Application of Membrane in Reaction Engineering for Green Synthesis -- Abstract -- 1 Introduction -- 2 Applications of Membrane Reactors in Reaction Engineering -- 2.1 Syngas Production -- 2.2 Hydrogen Production -- 2.3 CO2 Thermal Decomposition -- 2.4 Higher Hydrocarbon Production -- 2.5 Methane Production -- 2.6 Ammonia Production -- 3 Environmental Impacts -- 4 Conclusions and Future Recommendations -- Acknowledgements -- References -- 9 Photo-Enzymatic Green Synthesis: The Potential of Combining Photo-Catalysis and Enzymes -- Abstract -- 1 Introduction -- 2 Principle -- 3 Enzymes Involved in Light-Driven Catalysis -- 3.1 Heme-Containing Enzymes -- 3.1.1 Cytochrome P450 -- 3.1.2 Peroxidases -- 3.2 Flavin-Based Enzyme -- 3.2.1 Baeyer-Villiger Monooxygenases -- 3.2.2 Old Yellow Enzymes -- 3.3 Metal Cluster-Centered Enzyme -- 3.3.1 Hydrogenases -- 3.3.2 Carbon Monoxide Dehydrogenases -- 4 Nanoparticle-Based Activation of Enzyme -- 5 Applications in Photo-Biocatalysis -- 5.1 Isolated Enzymes/Cell Lysates -- 6 Summary and Future Scope -- References. , 10 Biomass-Derived Carbons and Their Energy Applications -- Abstract -- 1 Introduction -- 2 Types of Biomass Materials -- 2.1 Plant-Based Carbons -- 2.2 Fruit-Based Carbons -- 2.3 Animal-Based Carbons -- 2.4 Microorganism-Based Carbons -- 3 Activation of Biomass-Derived Carbons -- 3.1 Activation of Carbons -- 3.1.1 Chemical Activation of Carbons -- 3.1.2 Carbon Activation Through Physical Method -- 3.1.3 Self-activation of Carbons -- 3.2 Pyrolysis Techniques -- 3.2.1 Effect of Temperature -- 3.2.2 Effect of Residence Time -- 3.2.3 Heating Rate Effect -- 3.2.4 Size of the Particle -- 3.3 Microwave-Assisted Technique -- 3.4 Carbonization by Hydrothermal -- 3.5 Ionothermal Carbonization -- 3.6 Template Method -- 4 Energy Storage Applications of Biomass Carbons -- 4.1 Supercapacitors -- 4.2 Li/Na-Ion Batteries -- 5 Conclusion -- Acknowledgements -- References -- 11 Green Synthesis of Nanomaterials via Electrochemical Method -- Abstract -- 1 Introduction -- 2 Green Synthesis -- 2.1 Application of Biology in Green Synthesis -- 2.2 Green Synthesis Based on the Application of Solvent -- 3 Computational Data and Analysis -- 4 Electrochemical Method -- 5 Electrodeposition Method -- 5.1 Experimental Setup for Electrodeposition -- 6 Research Work: Using Green Electrochemical Methods for Nanomaterials Synthesis -- 7 Conclusion -- References -- 12 Microwave-Irradiated Synthesis of Imidazo[1,2-a]pyridine Class of Bio-heterocycles: Green Avenues and Sustainable Developments -- Abstract -- 1 Introduction -- 2 Microwave-Assisted Synthesis of 2-arylimidazo[1,2-a]pyridines [Abbreviated as 2-Aryl-IPs]. -- 2.1 Synthesis of Fused Bicyclic Heteroaryl Boronates and Imidazopyridine-Quinazoline Hybrids Under MW-irradiations -- 2.2 MW-Irradiated Synthesis of IPs Using Multi-Component Strategy Under Neat Conditions. , 2.3 One-Pot, Three-Component Synthesis of 2-Phenyl-H-Imidazo[1,2-α]pyridine Under MW-Irradiations -- 2.4 Microwave-Assisted Amine-Triggered Benzannulation Strategy for the Preparation of 2,8-Diaryl-6-Aminoimidazo-[1,2-a]pyridines -- 2.5 MW-Assisted NaHCO3-catalyzed Synthesis of Imidazo[1,2-a]pyridines in PEG400 Media and Its Practical Application in the Synthesis of 2,3-Diaryl-IP Class of Bio-Heterocycles -- 2.6 MW-Irradiated, Ligand-Free, Palladium-Catalyzed, One-Pot 3-component Reaction for an Efficient Preparation of 2,3-Diarylimidazo[1,2-a]pyridines -- 2.7 MW-Assisted Water-PEG400-mediated Synthesis of 2-Phenyl-IP via Multi-Component Reaction (MCR) -- 2.8 Microwave-Irradiated Synthesis of Imidazo[1,2-a]pyridines Under Neat, Catalyst-Free Conditions -- 2.9 Green Synthesis of Imidazo[1,2-a]pyridines in H2O -- 2.10 Microwave-Assisted Neat Synthesis of Substituted 2-Arylimidazo[1,2-a]Pyridines -- 2.11 Microwave-Assisted Nano SiO2 Neat Synthesis of Substituted 2-Arylimidazo[1,2-a]pyridines -- 2.12 Microwave-Assisted NaHCO3-Catalyzed Synthesis of 2-phenyl-IPs -- 3 Microwave-Assisted Synthesis of 3-amino-2-arylimidazo[1,2-a]pyridines [3-amino-2-aryl-IPs] -- 3.1 Microwave-Irradiated Synthesis of 3-aminoimidazo[1,2-a]pyridines via Fluorous Multi-component Pathway -- 3.2 MW-Irradiated Synthetic Protocol for 3-aminoimidazo[1,2-a]pyridines via MCR Pathway -- 3.3 MW-Assisted Sequential Ugi/Strecker Reactions Involving 3-Center-4-Component and 3-Center-5-Component MCR Strategy -- 3.4 One-Pot, 4-component Cyclization/Suzuki Coupling Leading to the Rapid Formation of 2,6-Disubstituted-3-Amino-IPs Under Microwave Irradiations -- 3.5 ZnCl2-catalyzed MCR of 3-aminoimidazo[1,2-a]pyridines Using MW Conditions -- 3.6 Microwave-Promoted Preparation of N-(3-arylmethyl-2-oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-Yl)Benzamides. , 3.7 MW-Assisted Multi-component Neat Synthesis of Benzimidazolyl-Imidazo[1,2-a]pyridines.

Anmerkung: Intro -- Preface -- Contents -- Contributors -- Chapter 1: Role of Nano-photocatalysis in Heavy Metal Detoxification -- 1.1 Introduction -- 1.2 Heavy Metals and Their Toxicological Effects -- 1.2.1 Cadmium -- 1.2.2 Chromium -- 1.2.3 Copper -- 1.2.4 Lead -- 1.2.5 Mercury -- 1.2.6 Nickel -- 1.2.7 Zinc -- 1.3 Overview of Photocatalysis -- 1.4 Mechanism of Photocatalysis -- 1.5 Types of Photocatalysis -- 1.5.1 Homogeneous Photocatalysis -- 1.5.2 Heterogeneous Photocatalysis -- 1.6 Overview and Mechanism of Nano-photocatalysis -- 1.7 Photocatalytic Nanoparticle Synthesis -- 1.7.1 Organic Synthesis -- 1.7.1.1 Plant Extracts Aqueous Solutions -- 1.7.1.2 Microorganisms -- 1.7.2 Chemical Synthesis -- 1.7.2.1 Sol-Gel Method -- 1.7.2.2 Hydrothermal Method -- 1.7.2.3 Polyol Synthesis -- 1.7.2.4 Precipitation Method -- 1.7.3 Physical Synthesis -- 1.7.3.1 Ball Milling -- 1.7.3.2 Melt Mixing -- 1.7.3.3 Physical Vapour Deposition (PVD) -- 1.7.3.4 Laser Ablation -- 1.7.3.5 Sputter Deposition -- 1.8 Mode of Operation on Nano-photocatalysis -- 1.9 Parameters Affecting the Photocatalytic Efficiency -- 1.9.1 Effect of pH of the Reaction Solution -- 1.9.2 Effect of Photocatalyst Concentration -- 1.9.3 Effect of Substrate Adsorption -- 1.9.4 Effect of Dissolved Oxygen -- 1.10 Application -- 1.10.1 Chromium -- 1.10.1.1 pH -- 1.10.1.2 Light Intensity -- 1.10.1.3 Photocatalyst Dosage -- 1.10.1.4 Presence of Organic Compounds -- 1.10.2 Mercury -- 1.10.3 Arsenic -- 1.10.4 Uranium -- 1.11 Disadvantages of Photocatalysis -- 1.12 Photocatalyst Modifications -- 1.12.1 Dye Sensitization -- 1.12.2 Ion Doping -- 1.12.3 Composite Semiconductor -- 1.13 Conclusion -- References -- Chapter 2: Solar Photocatalysis Applications to Antibiotic Degradation in Aquatic Systems -- 2.1 Introduction -- 2.2 Solar Photocatalysis Process. , 2.3 Solar Photocatalysis Treatment for Antibiotic Degradation -- 2.3.1 Trimethoprim -- 2.3.2 Sulfamethoxazole -- 2.3.3 Erythromycin -- 2.3.4 Ciprofloxacin -- 2.4 Conclusions -- References -- Chapter 3: Biomass-Based Photocatalysts for Environmental Applications -- 3.1 Introduction -- 3.2 Background of Biomass-Derived Carbon -- 3.2.1 Biochar -- 3.2.2 Activated Carbon (AC) -- 3.3 Synthesis Methods of Biomass-Derived Carbon -- 3.3.1 Pyrolysis -- 3.3.2 Hydrothermal Carbonization -- 3.3.3 Physical and Chemical Activation -- 3.4 Photocatalysts and Photocatalysis Reactions -- 3.5 Functionalized AC and Applications -- 3.5.1 Types of Functionalized AC -- 3.5.2 Functionalized AC Photocatalysts and Its Application -- 3.6 Future Challenges and Conclusions -- References -- Chapter 4: Application of Bismuth-Based Photocatalysts in Environmental Protection -- 4.1 Introduction -- 4.2 Photocatalytic Oxidation of Pharmaceuticals in Water -- 4.2.1 Tetracycline -- 4.2.2 Ciprofloxacin and Other Antibiotics -- 4.2.3 Carbamazepine -- 4.2.4 Ibuprofen and Diclofenac -- 4.2.5 Other Pharmaceuticals -- 4.3 Photocatalytic Oxidation of Industrial Micropollutants -- 4.3.1 Bisphenol A -- 4.3.2 Oxidation of Other Industrial Pollutants -- 4.4 Oxidation of the Indoor Air Pollutant NOx -- 4.5 Photocatalytic Reduction of Pollutants in Water and Air -- 4.5.1 Reduction of Cr(VI) in Water -- 4.5.2 Reduction of CO2 in Air -- 4.6 Water Splitting -- 4.7 Conclusions -- References -- Chapter 5: Phosphors-Based Photocatalysts for Wastewater Treatment -- 5.1 Introduction -- 5.2 Phosphor Materials: A Historical Background -- 5.3 Inorganic Phosphors in Photocatalysis -- 5.3.1 Types of Inorganic Phosphor Materials -- 5.3.2 Down-Conversion Phosphors in Photocatalysis -- 5.3.3 Up-Conversion Phosphors in Photocatalysis -- 5.3.4 Long-Persistent Phosphors in Photocatalysis. , 5.4 Organic Up-Conversion Phosphors in Photocatalysis -- References -- Chapter 6: Nanocarbons-Supported and Polymers-Supported Titanium Dioxide Nanostructures as Efficient Photocatalysts for Remedi... -- 6.1 Introduction -- 6.1.1 Heterogeneous Semiconductor Photocatalysis -- 6.1.2 Potential TiO2-Based Photocatalysts -- 6.1.3 Limitations of the Fine Powder Form of TiO2-Based Photocatalysts -- 6.1.3.1 Comparison of Synthesis Methods -- 6.1.3.2 Improvements in TiO2 Performance by Structural Change, Doping, and Hybridization -- 6.2 TiO2 Photocatalysts with Polymer-Based Hybrid Photocatalysts for Wastewater Treatment -- 6.2.1 Need for Immobilization of TiO2-Based Photocatalysts -- 6.2.1.1 Features of a Stable Substrate, and Available Substrates -- 6.2.1.2 Comparison of Polymeric Supports for Wastewater Treatment -- 6.3 TiO2 Photocatalysts Supported with Nanocarbons for Wastewater Treatment -- 6.3.1 TiO2-Functionalized Nanocarbon-Based Photocatalysts -- 6.3.1.1 Potential Photocatalytic Improvements with Carbon Nanostructures for Wastewater Treatment -- 6.4 Conclusions and Future Outlook -- References -- Chapter 7: Investigation in Sono-photocatalysis Process Using Doped Catalyst and Ferrite Nanoparticles for Wastewater Treatment -- 7.1 Introduction -- 7.2 Dependency of Catalytic Activity -- 7.2.1 Size-Dependent Catalytic Activity -- 7.2.2 Shape-Dependent Catalytic Effect -- 7.2.3 Interparticle Distance-Dependent Catalytic Effect -- 7.2.4 Support Interaction and Charge Transfer-Dependent Reactivity -- 7.3 Type of Nanoparticles -- 7.3.1 Non-metallic Nanoparticles -- 7.3.2 Metallic Nanoparticles -- 7.3.3 Semiconductor Nanoparticles -- 7.3.4 Ceramic Nanoparticles -- 7.3.5 Polymer Nanoparticles -- 7.3.6 Lipid-Based Nanoparticles -- 7.4 Types of Nanoparticles Based on Structure -- 7.5 Synthesis and Applications -- 7.5.1 Discussions -- 7.6 Synergetic Effect. , 7.7 Conclusion and Overview -- References -- Chapter 8: Magnetic-Based Photocatalyst for Antibacterial Application and Catalytic Performance -- 8.1 Introduction -- 8.2 Magnetic-Based Photocatalysts in Inactivation of the Microorganism -- 8.3 Factors Affecting the Photocatalytic Bacterial Inactivation -- 8.3.1 Effect of Magnetic-Based Photocatalyst Concentration and Light Intensity -- 8.3.2 Nature of Microorganism -- 8.3.3 Solution pH of Magnetic-Based Photocatalyst Suspension -- 8.3.4 Initial Bacterial Concentration -- 8.3.5 Physiological State of Bacteria -- 8.4 Proposed Mechanism for Bacteria Disinfection by the Magnetic-Based Photocatalyst -- 8.5 Using Magnetic-Based Catalyst in Photocatalytic Abatement of Organics -- 8.6 Photocatalysis for the Simultaneous Treatment of Bacteria and Organics -- 8.7 Conclusion and Future Prospects -- References -- Chapter 9: Antimicrobial Activities of Photocatalysts for Water Disinfection -- 9.1 Introduction -- 9.2 Mechanisms of Photocatalytic Disinfection -- 9.3 Pure and Modified Photocatalysts -- 9.4 Photocatalytic Films and Biofilms -- 9.5 Photocatalytic Composites and Nanocomposites -- 9.6 Materials with Antimicrobial Activity in the Absence of Light -- 9.7 Case Study: Application of Supported Photocatalysts in Disinfection of Whey-Processing Water -- 9.8 Final Considerations -- References -- Chapter 10: Medicinal Applications of Photocatalysts -- 10.1 Introduction -- 10.1.1 Background -- 10.2 Antifungal Activity -- 10.3 Virucidal Activity -- 10.4 Antimicrobial Activity -- 10.5 Anticancer Activity -- 10.6 Conclusion -- References -- Index.

Anmerkung: Intro -- Preface -- Contents -- 1 Green Approach: Microbes for Removal of Dyes and Metals via Ion Binding -- Abstract -- 1.1 Introduction -- 1.2 Pollutants in the Environment -- 1.2.1 Toxic Metals -- 1.2.2 Triphenylmethane Dyes -- 1.3 Bioremediation Approaches in Removing Pollutants -- 1.3.1 Non-microbial Strategies -- 1.3.2 Microbial-Based Strategies -- 1.4 Mechanisms for Removal of Pollutant Ions -- 1.4.1 Mechanisms for Removal of Metal Ions -- 1.4.2 Mechanisms for Removal of Dyes -- 1.5 Innovations in the Removal of Pollutant Ions -- 1.6 Conclusions and Future Prospects -- Acknowledgements -- References -- 2 Removal of Heavy Metal from Wastewater Using Ion Exchange Membranes -- Abstract -- 2.1 Introduction -- 2.2 Heavy Metal -- 2.2.1 Chromium -- 2.2.2 Nickel -- 2.2.3 Copper -- 2.2.4 Zinc -- 2.2.5 Cadmium -- 2.2.6 Mercury -- 2.2.7 Lead -- 2.3 Physical Treatment Methods -- 2.3.1 Ultrafiltration -- 2.3.2 Nanofiltration -- 2.3.3 Reverse Osmosis -- 2.3.4 Forward Osmosis -- 2.3.5 Adsorption -- 2.4 Chemical Treatment Methods -- 2.4.1 Electrodialysis Method -- 2.4.2 Fuel Cell Method -- 2.5 Remaining Challenges and Perspectives -- 2.6 Conclusion -- Acknowledgements -- References -- 3 Separation and Purification of Uncharged Molecules -- Abstract -- 3.1 Introduction -- 3.2 Separation and Purification of Vitamin B12 -- 3.2.1 Downstream Processing of Vitamin B12 for Measurement -- 3.3 Separation and Purification of Haemoglobin -- 3.4 Separation and Purification of Uncharged Dyes -- 3.4.1 Purification and Separation of Dyes -- 3.5 Conclusion -- References -- 4 Aluminosilicate Inorganic Polymers (Geopolymers): Emerging Ion Exchangers for Removal of Metal Ions -- Abstract -- 4.1 Introduction -- 4.2 Methodology and Calculations -- 4.2.1 Terminology: Ion Exchange or Adsorption -- 4.2.2 Evidence for Ion Exchange. , 4.2.3 Modeling of Adsorption of Metal Ions on Geopolymers -- 4.2.4 Geopolymer Preparation -- 4.2.5 Washing of the Geopolymeric Adsorbent -- 4.2.6 Comparison Between Geopolymers and Zeolites -- 4.2.7 Geopolymers as Ion Exchangers -- 4.2.7.1 Geopolymers as Ion Exchangers for Alkali Metal Ions -- 4.2.7.2 Geopolymers as Ion Exchangers for Ammonium Ion -- 4.2.7.3 Geopolymers as Ion Exchangers for Alkaline Earth Metals -- 4.2.7.4 Geopolymers as Ion Exchangers for Heavy Metals -- Metakaolin-Based Geopolymers -- Fly Ash-Based Geopolymers -- Zeolite-Based Geopolymers -- 4.2.7.5 Geopolymers as Ion Exchangers/Adsorbents for Cationic Organic Dyes -- 4.2.8 Comparison of Geopolymers with Zeolites -- 4.2.8.1 Synthesis Conditions -- 4.2.8.2 Crystallinity -- 4.2.8.3 Surface Area and Porosity -- 4.2.8.4 Cation Exchange Capacity -- 4.2.8.5 Selectivity for Metal Ions -- 4.2.8.6 Stability in Acidic Solutions -- 4.2.8.7 Thermal Stability -- 4.2.8.8 Mechanical Strength -- 4.2.8.9 Regeneration -- 4.2.9 Stabilization/Solidification/Encapsulation of Ion Exchangers in Geopolymers -- 4.3 Concluding Remarks -- References -- 5 Microwave-Assisted Hydrothermal Synthesis of Agglomerated Spherical Zirconium Phosphate for Removal of Cs+ and Sr2+ Ions from Aqueous System -- Abstract -- 5.1 Introduction -- 5.2 Materials and Methods -- 5.2.1 Preparation of Agglomerated Spherical Zirconium Phosphate -- 5.2.2 Characterization -- 5.2.3 Ion Exchange Properties -- 5.2.4 Elution Behaviour -- 5.2.5 Distribution Studies -- 5.3 Results and Discussion -- 5.3.1 Fourier-Transform Infrared (FT-IR) Characterization -- 5.3.2 Powder X-ray Diffraction Studies -- 5.3.3 Scanning Electron Microscopy (SEM) and Energy Dispersive (EDS) Characterization -- 5.3.4 Zeta and Surface Area Analysis -- 5.3.5 Ion Exchange Characteristics -- 5.3.6 Mechanism of Sr2+ Interaction with Zirconium Phosphate -- 5.4 Conclusion. , Acknowledgements -- References -- 6 Metal Hexacyanoferrates: Ion Insertion (or Exchange) Capabilities -- Abstract -- 6.1 Introduction -- 6.2 Ion Exchange -- 6.2.1 Ion Exchange in MHCF at Work: Potentiometric Ion Sensors -- 6.2.2 An Ion Exchange-Based Approach for the Recovery of Metal Ions: The Case of Cesium and Thallium -- 6.2.3 Electrochemically Driven Ion Exchange -- 6.2.4 Reversible Ion Insertion in Battery Systems -- 6.3 Conclusion -- References -- 7 Biosorbents and Composite Cation Exchanger for the Treatment of Heavy Metals -- Abstract -- 7.1 Introduction -- 7.2 Agro-Based Biosorbents for Heavy Metal Removal -- 7.3 Biopolymers -- 7.3.1 Functional Groups -- 7.3.2 Cellulose -- 7.3.3 Chitosan -- 7.3.4 Nanofiber Membranes and Packed-Bed Adsorbers -- 7.4 Composite Ion Exchangers -- 7.5 Conclusion and Future Outlook -- References -- 8 Rare Earth Elements-Separation Methods Yesterday and Today -- Abstract -- 8.1 Introduction -- 8.2 Rare Earth Elements -- 8.2.1 General Characteristics -- 8.2.2 The Occurrence of Rare Earth Elements -- 8.2.3 Physicochemical Properties of Rare Earth Elements -- 8.2.4 Application of Rare Earth Metals -- 8.2.5 Production and Consumption of Rare Earth Elements in the World -- 8.3 Rare Earth Element Recovery from Nickel-Metal Hydride Batteries -- 8.4 Rare Earth Element Recovery from Permanent Magnets -- 8.5 Separation of High-Purity Rare Earth Elements -- 8.5.1 Separations of Rare Earth Elements of High Purity Using Cation Exchangers -- 8.5.2 Separations of Rare Earth Elements of High Purity Using Anion Exchangers -- 8.5.3 Separations of Rare Earth Elements of High Purity Using Chelating Ion Exchangers -- 8.6 Current Technologies -- 8.7 Conclusions -- References -- 9 Sequestration of Heavy Metals from Industrial Wastewater Using Composite Ion Exchangers -- Abstract -- 9.1 Introduction -- 9.2 Ion-Exchange Materials. , 9.2.1 Organic Materials -- 9.2.2 Inorganic Materials -- 9.2.3 Composite Materials -- 9.2.3.1 Hybrid Materials -- 9.2.3.2 Nanocomposite -- 9.3 Mechanism of Ion-Exchange Process -- 9.4 Conclusion -- Acknowledgements -- References -- 10 Applications of Organic Ion Exchange Resins in Water Treatment -- Abstract -- 10.1 Introduction -- 10.2 Removal of Heavy Metals -- 10.3 Removal of Organics -- 10.3.1 Natural Organic Matter (NOM) -- 10.3.2 Disinfection by-Products (DBPs) -- 10.3.3 Surfactants -- 10.3.4 Pharmaceuticals -- 10.3.5 Dyes -- 10.3.6 Small Organic Matter -- 10.4 Desalination -- 10.5 Boron Removal -- 10.6 Removal of Anions -- 10.7 Removal of Cations -- 10.7.1 Hardness -- 10.7.2 Ammonium -- 10.8 Conclusions -- References.

Anmerkung: Intro -- Preface -- Acknowledgements -- Contents -- Contributors -- Chapter-1 -- Saving Solvents in Chromatographic Purifications: The Counter-Current Chromatography Technique -- 1.1 Introduction -- 1.2 CCC Theory -- 1.2.1 High Loadability -- 1.2.2 Scale up Capability -- 1.3 Instrumentation -- 1.3.1 Hydrostatic and Hydrodynamic Instruments -- 1.3.2 Liquid Systems -- 1.4 Counter Current Chromatography, a Green Process -- 1.4.1 Saving Solvents -- 1.4.2 Improving Process Parameters -- 1.4.3 Injecting Crude Samples -- 1.4.4 Greener Solvents -- 1.5 Counter Current Chromatography, a Tool for Green Chemistry Development -- 1.5.1 Natural Products -- 1.5.2 Solute Partition Coefficient Determination -- 1.6 Conclusion -- References -- Chapter-2 -- Ion Size Exclusion Chromatohtaphy on Hypercrosslinked Polystyrene Sorbents as a Green Technology of Separating Mineral Elecyrolites -- 2.1 Introduction -- 2.2 Nanoporous Hypercrosslinked Polystyrene Sorbents -- 2.3 Brief Description of Chromatographic Experiments -- 2.4 Dimensions of Hydrated Ions -- 2.5 Separation of Electrolytes on Nanoporous Hypercrosslinked Sorbents -- 2.6 Basic Features of Size Exclusion Chromatography -- 2.7 Conception of "Ideal Separation Process" -- 2.8 Selectivity of Electrolyte Separation Process -- 2.9 Influence of the Electrolyte Concentration on the Selectivity of Separat -- 2.10 "Acid Retardation", "Base Retardation" and "Salt Retardation" Phenomena -- 2.11 Other Convincing Proofs of Separating Electrolytes via Exclusion Mechanism -- 2.12 Do we Really Need Sorbent Functional Groups to Separate Electrolytes? -- 2.13 Productivity of the Ion Size Exclusion Process -- 2.14 Ion Size Exclusion-Green Technology -- 2.15 Conclusion -- References -- Chapter-3 -- Supercritical Fluid Chromatography: A Green Approach for Separation and Purification of Organic and Inorganic Analytes. , 3.1 Introduction to Green Chemistry and Supercritical Fluid Chromatography -- 3.2 Super Critical Fluids -- 3.2.1 Supercritical Fluid Extraction (SFE) -- 3.3 Supercritical Fluid Chromatography (SFC): An Overview -- 3.3.1 History of Development of Supercritical Fluid Chromatography -- 3.3.2 Instrumentation -- 3.3.2.1 Advantages and Disadvantages of Supercritical Fluid Chromatography -- 3.3.3 Properties of SFC compared to GC and HPLC -- 3.4 Industrial Applications of SCFs and SFCs -- 3.5 Conclusion -- References -- Chapter-4 -- High Performance Thin-Layer Chromatography -- 4.1 Introduction -- 4.2 High Performance Thin-Layer Chromatography -- 4.3 Sample Preparation in HPTLC -- 4.4 Green Separation Modalities in HPTLC -- 4.4.1 "Three R" Philosophy-Replacement of Toxic Solvents with Environmental Friendly Mobi -- 4.4.1.1 Reversed-Phase Chromatography -- 4.4.1.2 Hydrophilic Interaction Chromatography (HILIC) in HPTLC -- 4.4.1.3 Salting-Out Chromatography in HPTLC -- 4.5 Conclusion -- References -- Chapter-5 -- Green Techniques in Gas Chromatography -- 5.1 Introduction -- 5.2 Sample Preparation -- 5.2.1 Direct Methods Without Sample Preparation -- 5.2.2 Solventless Sample Preparation Techniques -- 5.2.2.1 Solid Phase Extraction -- 5.2.2.2 Vapor-Phase Extraction -- 5.2.2.3 Thermal Desorption (TD)/Thermal Extraction (TE) -- 5.2.2.4 Membrane Extraction -- 5.2.3 Sample Preparation Using Environmentally Friendly Solvents -- 5.2.3.1 Supercritical Fluid Extraction (SFE) -- 5.2.3.2 Subcritical Water Extraction (SWE) -- 5.2.3.3 Ionic Liquids (ILs) -- 5.2.3.4 Cloud-Point Extraction -- 5.2.4 Assisted Solvent Extraction -- 5.3 Column Considerations for Green Gas Chromatography -- 5.4 Carrier Gas Considerations for Green Gas Chromatography -- 5.5 Coupling GC with Other Analytical Tools -- 5.6 On-Site Analysis. , 5.7 Conclusion -- References -- Chapter-6 -- Preparation and Purification of Garlic-Derived Organosulfur Compound Allicin by Green Methodologies -- 6.1 Introduction -- 6.2 Green RP-HPLC Purification of the Allicin -- 6.3 Characterization of the Allicin by Green Methodologies -- 6.4 Allicin in Different Garlic Extract by Green RP-HPLC -- 6.5 Allicin Green Chemical Synthesis -- 6.6 Stability of Allicin -- 6.7 Conclusions -- References -- Chapter-7 -- Green Sample Preparation Focusing on Organic Analytes in Complex Matrices -- 7.1 Introduction -- 7.1.1 Trends in Green Analytical Chemistry -- 7.1.2 Green Techniques for Sample Preparation -- 7.1.2.1 Reduction and Solvent Replacement -- Supercritical Fluid Extraction -- Membranes -- 7.1.2.2 Solvent Elimination -- Solid Phase Extraction (SPE) -- Matrix Solid-Phase Dispersion (MSPD) -- Sorptive Extraction Techniques -- Solid Phase Microextraction (SPME) -- Stir-Bar Sorptive Extraction -- 7.2 Conclusions -- References -- Chapter-8 -- Studies Regarding the Optimization of the Solvent Consumption in the Determination of Organochlor -- 8.1 Introduction -- 8.2 Materials and Methods -- 8.2.1 Materials -- 8.2.2 Methods -- 8.3 Results -- 8.4 Discussions -- 8.4.1 TRM1 -- 8.4.2 TRM2 -- 8.5 Conclusions -- References -- Chapter-9 -- Size Exclusion Chromatography a Useful Technique For Speciation Analysis of Polydimethylsiloxanes -- 9.1 Introduction to SEC -- 9.2 SEC Retention Mechanisms -- 9.2.1 Ideal Size Exclusion Mechanism -- 9.2.2 Non-Ideal Size Exclusion Mechanism -- 9.3 The Stationary Phase in SEC -- 9.4 The Mobile Phase in SEC -- 9.5 Analytical Problems -- 9.6 Methods for Column Calibration -- 9.7 Applications of SEC Biomedical and Pharmaceutical -- 9.7.1 SEC as a Useful Technique for Linear Polydimethylsiloxanes Speciation Analysis. , 9.8 Methodology for Linear Polydimethylsiloxanes Speciation Analysis -- 9.8.1 Mobile Phase Selection -- 9.8.2 Stationary Phase Selection -- 9.8.3 Column Conditions -- 9.8.4 Column Calibration -- 9.8.5 Separation of Polydimethylsiloxanes -- 9.9 Conclusions -- References -- Erratum -- Index.

Anmerkung: Intro -- Contents -- 1 Chemical Valorization of CO2 -- Abstract -- 1 Introduction -- 2 CO2-Derived Fuels and Chemicals -- 2.1 Methane -- 2.2 Methanol -- 2.3 Dimethyl Ether -- 2.4 Formic Acid -- 2.5 Ethanol -- 2.6 CO2-Fischer-Tropsch Liquid Fuels -- 2.7 Carbon Monoxide-Syngas -- 3 CO2 Chemically Derived Materials -- 3.1 Polymers -- 3.2 CO2-Derived Building Materials -- 4 Conclusions -- References -- 2 Progress in Catalysts for CO2 Reforming -- Abstract -- 1 Introduction -- 2 Technologies for Capturing and Storing Carbon Dioxide -- 3 Technologies for Using Carbon Dioxide -- 4 Methane Dry Reforming Process -- 4.1 Progress in Catalysts for Methane Dry Reforming (1928-1989) -- 4.2 Progress in Catalysts for Methane Dry Reforming (1990-1999) -- 4.3 Progress in Catalysts for Methane Dry Reforming (2000-2009) -- 4.4 Progress in Catalysts for Methane Dry Reforming (2010-2019) -- 4.5 Current Status in the Catalysts for Methane Dry Reforming -- 5 Dry Reforming of Other Compounds -- 6 Use of Steam or Oxygen in Dry Reforming of Methane and Other Compounds -- 7 Solid Oxide Fuel Cells Fueled with Biogas -- 8 Commercialization of Dry Reforming Process -- 9 Conclusions -- References -- 3 Fuel Generation from CO2 -- Abstract -- 1 Introduction -- 2 Approaches for Directly Converting CO2 to Fuels -- 2.1 Pure CO2 Decomposition Technology -- 2.2 Reagent-Based CO2 Conversion Technology -- 2.2.1 Dry Deformation of Methane Technology -- 2.2.2 Catalytic Hydrogenation of CO2 -- 3 Biological CO2 Fixation for Fuels -- 3.1 Thermochemical Conversion -- 3.1.1 Torrefaction -- 3.1.2 Pyrolysis -- 3.1.3 Thermochemical Liquefaction -- 3.1.4 Gasification -- 3.1.5 Direct Combustion -- 3.2 Biochemical Conversion -- 3.2.1 Biodiesel -- 3.2.2 Bioethanol -- 3.2.3 Biomethane -- 3.2.4 Biohydrogen -- 3.2.5 Bioelectricity -- 3.2.6 Volatile Organic Compounds. , 4 Conclusion and Future Perspectives -- References -- 4 Thermodynamics of CO2 Conversion -- Abstract -- 1 Introduction -- 2 Carbon Dioxide Capture -- 3 Carbon Dioxide Utilisations -- 4 Thermodynamic Considerations -- 5 Thermodynamics of CO2 -- 5.1 The Thermodynamic Attainable Region (AR) -- 5.2 Using Hess's Law to Transform the Extents to G-H AR @ 25˚C -- 5.3 Increasing Temperature on G-H AR -- 6 Conclusion -- Acknowledgements -- References -- 5 Enzymatic CO2 Conversion -- Abstract -- 1 Introduction -- 1.1 CO2 as a Greenhouse Gas -- 1.2 Carbon Capture, Storage, and Utilization -- 1.3 CO2 as a Chemical Feedstock -- 1.4 CO2 Conversion with Enzymes -- 2 Natural Conversion of CO2 in Cells -- 3 Enzymatic Conversion of CO2 in Cells -- 3.1 Conversion of CO2 by a Single Enzyme (in vitro) -- 3.1.1 Formate Dehydrogenase -- 3.1.2 Carbonic Anhydrase -- 3.1.3 Carbon Monoxide Dehydrogenase -- 3.1.4 Ribulose-1,5-bisphosphate Carboxylase/Oxygenase (RuBisCO) -- 3.2 Conversion of CO2 by a Multi-Enzyme Cascade in vitro -- 3.3 Other Ways (Photocatalytic CO2 Methanation) -- 4 Industrial Applications -- 4.1 Alcohols -- 4.2 Organic Acids -- 4.3 Terpenoids -- 4.4 Fatty Acids -- 4.5 Polyhydroxyalkanoates -- 4.6 Calcium Carbonate -- 5 Summary and Future Prospects -- References -- 6 Electrochemical CO2 Conversion -- Abstract -- 1 Introduction -- 2 Electrochemical CO2 Conversion -- 2.1 Fundamentals of the Process -- 2.2 Variants of Electrochemical Conversion of CO2 -- 2.2.1 Aqueous Electrolytes -- 2.2.2 Non-Aqueous Electrolytes -- 2.2.3 Solid Oxide Electrolytes -- 2.2.4 Molten Salt Electrolytes -- 3 Electrochemical CO2 Conversion from Molten Salts -- 3.1 Present State of Electrochemical Reduction of CO2in Molten Salts for the Production of Solid-Phase Carbonaceous Nanomaterials -- 3.2 Direct Electrochemical Reduction of CO2 in Chloride Melts. , 3.3 Indirect Electrochemical Reduction of CO2 in Molten Salts -- 3.4 The Mechanisms of Electrode Reactions Occurring at the Cathode and Anode -- 3.5 Prospects for CO2 Conversion in Molten Salts -- 4 Conclusions -- References -- 7 Supercritical Carbon Dioxide Mediated Organic Transformations -- Abstract -- 1 Introduction -- 2 Applications of Supercritical Carbon Dioxide -- 2.1 Hydrogenation Reactions -- 2.2 Asymmetric Hydrogenation Reactions -- 2.3 Diels-Alder Reaction -- 2.4 Coupling Reaction -- 2.5 Oxidation Reaction -- 2.6 Baeyer-Villiger Oxidation Reaction -- 2.7 Iodination Reaction -- 2.8 Polymerization Reaction -- 2.9 Carbonylation Reaction -- 2.9.1 Acetalization Reaction -- 2.9.2 Olefin Metathesis Reaction -- 2.9.3 Synthesis of heterocycles -- Synthesis of α-alkylidene Cyclic Carbonates -- Synthesis of 4-Methyleneoxazolidin-2-Ones -- Synthesis of 5-Alkylidene-1, 3-Oxazolidin-2-Ones -- Synthesis of 6-Phenyl-3a, 4-Dihydro-1H-Cyclopenta[C]furan-5(3H)-One -- Synthesis of 3, 4, 5, 6-Tetraethyl-2H-Pyran-2-One -- 3 Conclusions -- Acknowledgements -- References -- 8 Theoretical Approaches to CO2 Transformations -- Abstract -- 1 Carbon Dioxide Properties -- 2 CO2 Transformation as an Undeniable Necessity -- 3 CO2 Activation -- 3.1 Methodologies of CO2 Activation -- 4 Theoretical Insight of CO2 Transformation -- 4.1 The Theoretical Approach in CO2 Conversion to Value-Added Chemicals -- 4.1.1 Carbon Monoxide -- 4.1.2 Methane -- 4.1.3 Methanol -- 4.1.4 Formic Acid -- 4.1.5 Heterocycles -- Cyclic Carbonates -- Cyclic Carbamate -- Quiznazoline-2,4(1H,3H)-Dione -- 4.1.6 Summary and Outlook -- 5 Theoretical Designing of Novel Catalysts Based on DFT Studies -- 5.1 Theoretical Designing: Problems and Opportunities -- 6 Conclusion -- References -- 9 Carbon Dioxide Conversion Methods -- Abstract -- 1 Introduction -- 2 Molecular Structure of CO2. , 3 Thermo-Kinetics of CO2 Conversion -- 4 CO2 Conversion Methods and Products -- 4.1 Fischer-Tropsch Gas-to-Liquid (GTL) -- 4.2 Mineralization -- 4.3 Chemical Looping Dry Reforming -- 4.4 Enzymatic Conversion -- 4.5 Photocatalytic and Photo-Electrochemical Conversion -- 4.6 Thermo-Chemical Conversion -- 4.7 Hydrogenation -- 4.8 Reforming -- 5 Economic Assessment of CO2Alteration to Valuable Products -- 5.1 Syngas -- 5.2 Methanol -- 5.3 Formic Acid -- 5.4 Urea -- 5.5 Dimethyl Carbonate (DMC) -- 6 Conclusions and Future Perspective -- Acknowledgements -- References -- 10 Closing the Carbon Cycle -- Abstract -- 1 Introduction -- 2 Methods to Capture CO2 -- 3 CO2 Capture Technologies -- 4 CO2 Capture from the Air -- 5 Biomass and Waste-Based Chemicals -- 6 Advantages of Biomass-Based Chemicals -- 7 Replacement of Carbon-Based Energy Resources -- 8 Biomass Energy -- 9 Wind Energy -- 10 Solar Energy -- 11 Ocean Energy -- 12 Geothermal Energy -- 13 Hydrothermal Energy -- 14 Conclusions -- References -- 11 Carbon Dioxide Utilization to Energy and Fuel: Hydrothermal CO2 Conversion -- Abstract -- 1 Introduction -- 2 Hydrothermal CO2 Conversion -- 2.1 Metals and Catalysts as Reductant -- 2.2 Organic Wastes as Reductant -- 2.3 Inorganic Wastes as Reductant -- 2.4 Biomass as Reductant -- 3 Conclusion -- References -- 12 Ethylenediamine-Carbonic Anhydrase Complex for CO2 Sequestration -- 1 Introduction -- 2 An Overview of Carbonic Anhydrase (CA) -- 3 Mechanism of Action for Biocarbonate Formation -- 4 Historical Background of Carbonic Anhydrase -- 5 Sources of Carbonic Anhydrase -- 6 Carbonic Anhydrase in Microorganism -- 6.1 Micrococcus Lylae, Micrococcus Luteus, and Pseudomonas Fragi -- 6.2 Bacillus Subtilis and Citrobacter Freundii -- 6.3 Neisseria Gonorrhoeae -- 6.4 Helicobacter Pylori -- 7 Plant Carbonic Anhydrase -- 8 Overview of CO2. , 9 Sources of Carbon Dioxide (CO2) -- 10 Effect of Carbon Dioxide (CO2) -- 11 Carbon Dioxide Capturing -- 12 Carbon Dioxide (CO2) Sequestration -- 13 Carbon Dioxide (CO2) Sequestration by Carbonic Anhydrase -- 14 Separation System for CO2 Sequestration -- 15 Cryogenic Separation -- 16 Membrane Separation -- 17 Absorption -- 18 Adsorption -- 19 Bioreactors for CO2 Sequestration -- 20 Carbonic Anhydrase Immobilization -- 21 Ethylenediamine for Carbon Dioxide (CO2) Capturing -- 22 CO2 Capturing and Sequestration with Ethylenediamine-Carbonic Anhydrase Complex -- 23 CO2 Capturing and Sequestration Design and Optimization: Challenges and Future Prospects -- 24 Conclusion -- References -- 13 Green Pathway of CO2 Capture -- Abstract -- 1 Introduction -- 2 Molecular Structure of Carbon Dioxide -- 3 CO2 Capture System -- 3.1 Post-Combustion System -- 3.2 Pre-Combustion System -- 3.3 Oxy-Fuel Combustion System -- 4 Absorption Technology -- 4.1 Green Absorption with Ionic Liquids -- 4.1.1 Properties and Uses of Ionic Liquids -- 4.1.2 CO2 Solubility in PILs -- 4.1.3 CO2 Absorption in PILs with Carboxylate Anion -- 4.2 Reaction Mechanism Involved in CO2-Absorption -- 5 Adsorption Technology -- 5.1 Organic Adsorbents -- 5.1.1 Activated Charcoal -- 5.1.2 Biochar -- 5.1.3 Metal-Organic Frameworks (MOFs) -- 5.2 Other CO2 Adsorbents -- 5.2.1 Metal Oxide-Based Absorbents -- 5.2.2 Zeolites -- 5.3 Biological Processes of CO2Sequestration -- 5.3.1 Carbon Utilization by Forest and Agricultural Management -- 5.3.2 Ocean Fertilization -- 5.3.3 CO2 Capture by Microalgae -- 5.4 Electrochemical Ways for CO2 Capture -- 6 Conclusion -- References -- 14 Carbon Derivatives from CO2 -- Abstract -- 1 Introduction -- 2 Artificial Photoreduction -- 3 Electrochemical Reduction -- 4 Hydrogenation -- 5 Synthesis of Organic Carbonates -- 6 Reforming. , 7 Photocatalytic Reduction of CO2 with Water.

Anmerkung: Intro -- Green Solvents II -- Preface -- Editor's Biography -- Acknowledgments -- Contents -- Contributors -- Chapter 1: Ionic Liquids as Green Solvents: Progress and Prospects -- 1.1 Introduction -- 1.2 History of Ionic Liquids (ILs) -- 1.3 Structure of Ionic Liquids (ILs) -- 1.3.1 Cations -- 1.3.2 Anions -- 1.4 Synthesis of Ionic Liquids (ILs) -- 1.4.1 Quaternization Reactions -- 1.4.2 Anion-Exchange Reactions -- 1.4.2.1 Lewis-Acid-Based Ionic Liquids (ILs) -- 1.4.2.2 Anion Metathesis -- 1.5 Properties of Ionic Liquids (ILs) -- 1.5.1 Melting Point -- 1.5.2 Volatility -- 1.5.3 Thermal Stability -- 1.5.4 Viscosity -- 1.5.5 Density -- 1.5.6 Polarity -- 1.5.7 Conductivity and Electrochemical Window -- 1.5.8 Toxicity -- 1.5.9 Air and Moisture Stability -- 1.5.10 Cost and Biodegradability -- 1.6 Solvent Properties and Solvent Effects -- 1.6.1 Solute-Ionic Liquids (ILs) Interactions -- 1.6.1.1 Interaction of Ionic Liquids (ILs) with Water -- 1.6.1.2 Interaction of Ionic Liquids (ILs) with Acid and Base -- 1.6.1.3 Interaction of Ionic Liquids (ILs) with Aromatic Hydrocarbon -- 1.6.1.4 Interaction with Chiral Substrates -- 1.7 Conclusions -- References -- Chapter 2: Ionic Liquids as Green Solvents for Alkylation and Acylation -- 2.1 Introduction -- 2.2 Alkylation -- 2.2.1 Ionic Liquids as Green Solvents -- 2.2.2 Ionic Liquids as Dual Green Solvents and Catalysts -- 2.2.3 Ionic Liquids Immobilized on Solid Supports -- 2.3 Acylation -- 2.3.1 Ionic Liquids as Green Solvents -- 2.3.2 Ionic Liquids in Dual Role as Green Solvents and Catalysts -- 2.3.3 Immobilized Ionic Liquids -- 2.4 Remarks -- References -- Chapter 3: Ionic Liquids as Green Solvents for Glycosylation Reactions -- 3.1 Introduction -- 3.2 Preparation of Acid-Ionic Liquids -- 3.3 Reusability of Acid-Ionic Liquids -- 3.4 Tunability and Basicity of Ionic Liquids. , 3.5 Nonvolatility of Ionic Liquids -- 3.6 Conclusions -- References -- Chapter 4: Ionic Liquid Crystals -- 4.1 Introduction -- 4.2 Ionic Liquid Crystals Based on Organic Cationsand Anions -- 4.2.1 Imidazolium-Based Ionic Liquid Crystals -- 4.2.2 Pyrrolidinium-Based Ionic Liquid Crystals -- 4.2.3 Pyridinium and Bipyridinium-Based IonicLiquid Crystals -- 4.2.4 Morpholinium-, Piperazinium-, and Piperidinium-BasedIonic Liquid Crystals -- 4.2.5 Ammonium-Based Ionic Liquid Crystals -- 4.2.6 Guanidinium-Based Ionic Liquid Crystals -- 4.2.7 Phosphonium-Based Ionic Liquid Crystals -- 4.2.8 Anions -- 4.3 Ionic Liquid Crystals Based on Metal Ions -- 4.4 Polymeric Ionic Liquid Crystals -- 4.4.1 Main-Chain Ionic Liquid-Crystalline Polymers -- 4.4.2 Side-Chain Ionic Liquid-Crystalline Polymers -- 4.4.3 Dendrimers -- 4.5 Applications of Ionic Liquid Crystals -- 4.6 Conclusions -- References -- Chapter 5: Application of Ionic Liquids in Extraction and Separation of Metals -- 5.1 Introduction -- 5.2 Processing Metal Oxides and Ores with Ionic Liquids -- 5.2.1 Metal Oxides Processing -- 5.2.2 Mineral Processing -- 5.3 Electrodeposition of Metals Using Ionic Liquids -- 5.3.1 Electrodeposition of Aluminum -- 5.3.2 Electrodeposition of Magnesium -- 5.3.3 Electrodeposition of Titanium -- 5.4 Ionic Liquids in Solvent Extraction of Metal Ions -- 5.5 Conclusions -- References -- Chapter 6: Potential for Hydrogen Sulfide Removal Using Ionic Liquid Solvents -- 6.1 Introduction -- 6.2 Ionic Liquids as Physical Solvents for H 2 S Removal -- 6.3 Hybrid Solvents Comprising Ionic Liquids and Amines -- 6.4 Conclusions and Outlook -- References -- Chapter 7: Biocatalytic Reactions in Ionic Liquid Media -- 7.1 Introduction -- 7.2 Biocatalyst Tested in Ionic Liquids -- 7.2.1 Lipases -- 7.2.2 Esterases and Proteases -- 7.2.3 Glycosidases -- 7.2.4 Oxidoreductases. , 7.3 Effect of the Ionic Liquid Composition on the Activity and Stability of Enzymes -- 7.4 Biotransformation in Ionic Liquids -- 7.4.1 Synthesis of Flavour Esters -- 7.4.2 Biotransformations of Polysaccharides and Nucleotides -- 7.4.3 Synthesis of Biodiesel -- 7.4.4 Synthesis of Polyesters -- 7.4.5 Resolution of Racemates -- 7.4.6 Synthesis of Carbohydrates -- 7.5 Conclusions -- References -- Chapter 8: Ionic Liquids/Supercritical Carbon Dioxide as Advantageous Biphasic Systems in Enzymatic Synthesis -- 8.1 Introduction -- 8.2 Supercritical Carbon Dioxide in Enzymatic Synthesis -- 8.3 Ionic Liquids as Reaction Media in Enzymatic Synthesis -- 8.4 Supercritical Carbon Dioxide/Ionic Liquid Biphasic System in Enzymatic Synthesis -- 8.5 Conclusions -- References -- Chapter 9: Ionic Liquids as Lubricants -- 9.1 Introduction -- 9.2 Overview of Ionic Liquids (ILs) -- 9.2.1 Definition and Types of Ionic Liquids (ILs) -- 9.2.2 Relationship Between Molecular Structure and Properties of Ionic Liquids (ILs) -- 9.3 Common Ionic Liquids (ILs) as Lubricants -- 9.3.1 Ionic Liquids (ILs) as Lubrication Oils -- 9.3.1.1 Ionic Liquids (ILs) as Lubrication Oils for Fe Alloy/Steel or Steel/Steel Contacts -- 9.3.1.2 Ionic Liquids (ILs) as Lubrication Oils of Light Alloys -- 9.3.1.3 Ionic Liquids (ILs) as Lubrication Oils for Specific Contacts -- 9.3.1.4 Ionic Liquids (ILs) as Lubrication Oils Under Vacuum -- 9.3.2 Ionic Liquids (ILs) as Lubrication Additives -- 9.3.2.1 Ionic Liquids (ILs) as Water Additives -- 9.3.2.2 Ionic Liquids (ILs) as Mineral Oil Additives -- 9.3.2.3 Ionic Liquids (ILs) as Synthetic Oil and Lubrication Grease Additives -- 9.3.2.4 Ionic Liquids (ILs) as Polymer Material Additives -- 9.3.3 Additives of Ionic Liquid (IL) Lubricants -- 9.3.4 Thin Films -- 9.4 Function of Ionic Liquids (ILs) as Lubricants. , 9.4.1 Function of Ionic Liquids (ILs) as Lubrication Oils -- 9.4.2 Function of Ionic Liquids (ILs) as Additives or Thin Films -- 9.5 Lubrication Mechanism -- 9.6 Conclusions and Outlook -- References -- Chapter 10: Stability and Activity of Enzymes in Ionic Liquids -- 10.1 Introduction -- 10.1.1 Ionic Liquid in Reference to Its Origin -- 10.1.2 Ionic Liquid as a Solvent -- 10.1.3 Enzymes in Ionic Liquids -- 10.2 Enzyme Stability in Ionic Liquids -- 10.2.1 Stability of Lipases -- 10.2.2 Stability of Monellin -- 10.2.3 Stability of Cytochrome c -- 10.2.4 Stability of α -Chymotrypsin -- 10.2.5 Stability of Penicillin G Acylase -- 10.3 Methods of Stabilizing Proteins/Enzymes in Ionic Liquids -- 10.3.1 Stabilization by Ionic Liquid Coating -- 10.3.2 Stabilization by Anchoring with Carbon Nanotubes -- 10.3.3 Stabilization by Capping with Nanoparticles -- 10.3.4 Stabilization by Entrapment in Hydrogels -- 10.3.5 Stabilization by Enzyme Modification -- 10.3.6 Stabilization by Emulsification of Ionic Liquids -- 10.4 Catalytic Activity of Enzymes in Ionic Liquids -- 10.4.1 Biotransformations by Lipases and Esterases -- 10.4.1.1 Esterification and Transesterification Reaction -- 10.4.1.2 Enantioselective Hydrolysis Reaction -- 10.4.1.3 Enantioselective Acylation Reaction -- 10.4.1.4 Kinetic Resolution of Alcohols -- 10.4.2 Reactions Catalyzed by Proteases -- 10.4.3 Carbohydrate Synthesis by Glycosidases -- 10.4.4 Hydrocyanation Reaction by Lyases -- 10.4.5 Biocatalytic Redox Reactions by Oxidoreductases -- 10.4.6 Enzymatic Polymerization Reaction in Ionic Liquids -- 10.5 Stability/Activity Vis-à-vis Solvent Property of Ionic Liquids: A Structure-Activity Relationship (SAR) Analysis -- 10.6 Conclusions -- References -- Chapter 11: Supported Ionic Liquid Membranes: Preparation, Stability and Applications -- 11.1 Introduction. , 11.2 Methods of Preparation and Characterization of Supported Ionic Liquid Membranes -- 11.3 Stability of Supported Ionic Liquid Membranes -- 11.4 Mechanism of Transport Through Supported Ionic Liquid Membranes -- 11.5 Fields of Application of Supported Liquid Membranes -- 11.6 Conclusions -- References -- Chapter 12: Application of Ionic Liquids in Multicomponent Reactions -- 12.1 Introduction -- 12.1.1 Ionic Liquids Based on 1-Butyl-3-methylimidazolium -- 12.1.1.1 1-Butyl-3-methylimidazolium -- 12.1.1.2 1-Butyl-3-methylimidazolium Hexafluorophosphate -- 12.1.1.3 1-n-Butyl-3-methylimidazolium Bromide -- 12.1.1.4 Butyl Methyl Imidazolium Hydroxide -- 12.1.1.5 Other 1-Butyl-3-methylimidazolium-Based Ionic Liquids -- 12.1.2 Other Imidazole-Based Ionic Liquids -- 12.1.2.1 Ionic Liquid-Supported Iodoarenes -- 12.1.2.2 1,3- n -Dibutylimidazolium Bromide -- 12.1.2.3 1- n -Butylimidazolium Tetrafluoroborate -- 12.1.2.4 1-Ethyl-3-methylimidazole Acetate -- 12.1.2.5 An Acidic Ionic Liquid -- 12.1.2.6 Task-Specific Ionic Liquids -- 12.1.2.7 1-Methyl-3-heptyl-imidazolium Tetrafluoroborate -- 12.1.2.8 1-[2-(Acetoacetyloxy)ethyl]-3-methylimidazolium Hexafluorophosphate-Bound Acetoacetate -- 12.1.2.9 1-[2-(Acetoacetyloxy)ethyl]-3-methylimidazolium Tetrafluoroborate- or Hexafluorophosphate-Bound b -oxo Esters -- 12.1.2.10 1-(2-Hydroxyethyl)-3-methylimidazolium Tetrafluoroborate or Hexafluorophosphate and N -(2-Hydroxyethyl)pyridinium Tetrafluoroborate or Hexafluorophosphate -- 12.1.2.11 PEG-1000-Based Dicationic Acidic Ionic Liquid -- 12.1.2.12 1-Ethyl-3-methylimidazolium ( S)-2-Pyrrolidinecarboxylic Acid Salt -- 12.1.2.13 1-Methyl-3-pentylimidazolium Bromide -- 12.1.2.14 3-Methyl-1-sulfonic Acid Imidazolium Chloride -- 12.1.3 Other Ionic Liquids -- 12.2 Conclusions -- References. , Chapter 13: Ionic Liquids as Binary Mixtures with Selected Molecular Solvents, Reactivity Characterisation and Molecular-Microscopic Properties.

Anmerkung: Intro -- Ion Exchange Technology II -- Preface -- Editors' Bios -- Contents -- Contributors -- List of Abbreviations -- Chapter 1: Separation of Amino Acids, Peptides, and Proteins by Ion Exchange Chromatography -- Chapter 2: Application of Ion Exchanger in the Separation of Whey Proteins and Lactin from Milk Whey -- Chapter 3: Application of Ion Exchangers in Speciation and Fractionation of Elements in Food and Beverages -- Chapter 4: Applications of Ion Exchangers in Alcohol Beverage Industry -- Chapter 5: Use of Ion Exchange Resins in Continuous Chromatography for Sugar Processing -- Chapter 6: Application of Ion Exchange Resins in the Synthesis of Isobutyl Acetate -- Chapter 7: Therapeutic Applications of Ion Exchange Resins -- Chapter 8: Application of Ion Exchange Resins in Kidney Dialysis -- Chapter 9: Zeolites as Inorganic Ion Exchangers for Environmental Applications: An Overview -- Chapter 10: Ion Exchange Materials and Environmental Remediation -- Chapter 11: Metal Recovery, Separation and/or Pre-concentration -- Chapter 12: Application of Ion Exchange Resins in Selective Separation of Cr(III) from Electroplating Effluents -- Chapter 13: Effect of Temperature, Zinc, and Cadmium Ions on the Removal of Cr(VI) from Aqueous Solution via Ion Exchange with Hydrotalcite -- Chapter 14: An Overview of '3d' and '4f' Metal Ions: Sorption Study with Phenolic Resins -- Chapter 15: Inorganic Ion Exchangers in Paper and Thin-Layer Chromatographic Separations -- Chapter 16: Cation-Exchanged Silica Gel-Based Thin-Layer Chromatography of Organic and Inorganic Compounds -- Chapter 17: Ion Exchange Technology: A Promising Approach for Anions Removal from Water -- Index.

Anmerkung: Intro -- Preface -- Contents -- Contributors -- Chapter 1: Nanophotocatalysts for Fuel Production -- 1.1 Introduction -- 1.2 Quantum Dot Semiconductors -- 1.3 Synthesis of Quantum Dots -- 1.4 Application of Quantum Dots for Fuel Production -- 1.5 Conclusion -- References -- Chapter 2: Highly Stable Metal Oxide-Based Heterostructured Photocatalysts for an Efficient Photocatalytic Hydrogen Production -- 2.1 Photocatalysis -- 2.1.1 Photocatalytic Mechanism -- 2.1.2 Band Edge Positions -- 2.2 Semiconducting Metal Oxides for Photocatalytic Water Splitting -- 2.2.1 Metal Oxide-Based Heterostructured Photocatalysts -- 2.2.1.1 Energy Structure of TiO2 -- 2.2.1.2 Lattice Structure of TiO2 -- 2.3 The Challenges in Photocatalytic H2 Production Using TiO2 Particulate Systems -- 2.4 Strategies for Improving TiO2 Photocatalytic Activity -- 2.4.1 Addition of Sacrificial Reagents -- 2.4.2 TiO2-Based Semiconductors Under UV Light Irradiation -- 2.4.3 Photocatalytic Performance of TiO2 Under Visible Irradiation -- 2.4.4 Functionalization of TiO2 with Carbon Nanomaterials -- 2.4.4.1 Carbon Nanotubes -- 2.4.4.2 Graphene Oxide/Reduced Graphene Oxide (RGO) -- 2.5 Future Scope/Conclusions -- References -- Chapter 3: Novelty in Designing of Photocatalysts for Water Splitting and CO2 Reduction -- 3.1 Introduction -- 3.2 CO2 Reduction -- 3.2.1 Principles of CO2 Reduction -- 3.2.2 By-Products of CO2 Reduction -- 3.2.3 Synthesis of Nanoparticles -- 3.2.3.1 Doping of Photocatalyst -- 3.2.4 Commercial Challenges of CO2 Reduction -- 3.3 Water Splitting -- 3.3.1 The Basic Principle of Water Splitting -- 3.3.2 Photocatalyst for Water Splitting -- 3.3.2.1 Oxide-Based Photocatalyst -- 3.3.2.2 Nitride-Based Photocatalyst -- 3.3.3 Commercial Challenges of Water Splitting -- 3.4 Conclusion and Way Forward -- References. , Chapter 4: Z-Scheme Photocatalysts for the Reduction of Carbon Dioxide: Recent Advances and Perspectives -- 4.1 Introduction -- 4.2 Basic Principles of the Z-Scheme Reduction of CO2 -- 4.3 Advances in Z-Scheme Photocatalytic Reduction of CO2 -- 4.3.1 Z-Scheme Systems with Aqueous Shuttle Redox Mediator -- 4.3.2 All-Solid-State Z-Scheme Systems -- 4.3.3 Semiconductor/Metal-Complex Hybrid Z-Scheme Systems -- 4.3.4 Light Harvesting of Photocatalysts Utilized for the Z-Scheme CO2 Reduction -- 4.3.5 Cocatalyst Strategies for Z-Scheme CO2 Reduction -- 4.4 Summary and Outlook -- References -- Chapter 5: Photocatalysts for Artificial Photosynthesis -- 5.1 Introduction -- 5.2 General Photosynthesis Mechanism -- 5.3 Covalently Linked Molecular Systems for Artificial Photosynthesis -- 5.3.1 Porphyrin-Based Donor-Acceptor Molecular Systems -- 5.3.2 Subphthalocyanine-Based Light-Harvesting Complexes -- 5.3.3 BODIPY-Based Light-Harvesting Systems -- 5.4 Supramolecular Artificial Photosynthetic Systems -- 5.4.1 Metal-Ligand Interactions of Porphyrins/Naphthalocyanines with Electron Acceptors -- 5.4.2 Supramolecular Photosynthetic Complexes Via Crown Ether-Ammonium Cation Interactions -- 5.5 Conclusion -- References -- Chapter 6: Polymeric Semiconductors as Efficient Photocatalysts for Water Purification and Solar Hydrogen Production -- 6.1 Introduction -- 6.2 Photocatalysis -- 6.2.1 Basic Principles of Photocatalytic Reaction -- 6.2.2 Photocatalytic Properties -- 6.2.3 Photocatalytic Mechanism -- 6.3 Photocatalytic Functional Materials: Synthesis, Properties and Applications -- 6.3.1 Graphitic Carbon Nitride (g-C3N4) -- 6.3.1.1 Synthesis of Polymeric g-C3N4 -- 6.3.1.2 Photocatalytic Mechanism of g-C3N4 -- 6.3.1.3 Photodegradation of Chemical Pollutants Using g-C3N4 -- 6.3.1.4 Graphene Oxide-Based Hybrid Photocatalysts. , 6.3.2 Metal-Organic Framework (MOF)-Based Photocatalysts -- 6.3.2.1 Principles -- 6.3.2.2 Photocatalytic Applications of MOFs -- 6.3.3 TiO2-Based Hybrid Photocatalysts -- 6.3.3.1 Principles -- 6.3.3.2 Different Forms of TiO2 and Its Physicochemical Properties -- 6.3.3.3 Structure of TiO2 -- 6.3.3.4 Photocatalytic Mechanism of TiO2 -- 6.3.3.5 Hybrid Photocatalysts Based on TiO2 and Organic Conjugated Polymers -- 6.3.3.5.1 Properties of Polythiophene -- 6.3.3.5.2 Properties of Polyaniline -- 6.3.3.5.3 Properties of Polypyrrole -- 6.3.3.5.4 Synthesis of TiO2-Based Hybrid Photocatalysts with Different Organic Conjugated Polymers -- 6.3.3.5.5 Characterization of TiO2/Conjugated Polymer-Based Hybrid Catalysts -- 6.3.3.5.6 Antibacterial Activity of Photocatalysts -- 6.3.3.6 Environmental Application of Different Photocatalysts -- 6.3.3.6.1 Water Purification -- 6.3.4 Graphene Oxide (GO)-Based Photocatalyst for Dye Degradation and H2 Evolution -- 6.3.4.1 Photodegradation of Chemical Pollutants -- 6.3.4.2 Hydrogen (H2) Evolution Reaction by g-C3N4-Based Functional Photocatalysts -- 6.4 Conclusion -- References -- Chapter 7: Advances and Innovations in Photocatalysis -- 7.1 Introduction -- 7.2 Photocatalysts for Hydrogen Production -- 7.2.1 Nature of Different Sacrificial Agents and Typical Mechanism of Photoreforming -- 7.2.1.1 Methanol as a Sacrificial Agent -- 7.2.1.2 Ethanol as a Sacrificial Agent -- 7.2.1.3 Glycerol as a Sacrificial Agent -- 7.2.1.4 Glucose as a Sacrificial Agent -- 7.2.2 Hydrogen Production from Photocatalytic Wastewater Treatment -- 7.3 Photocatalysts Developed for the Synthesis of Organic Compounds in Mild Conditions -- 7.3.1 The Starting Point -- 7.3.2 The Effect of Supporting Metal Oxides on Titania on Selectivity -- 7.3.3 The Effect of Titania Dopant -- 7.3.4 The Effect of Titania Surface Area. , 7.3.5 The Effect of Substituting Titania -- 7.3.6 The Effect of Reactor and Illumination -- 7.3.7 Cyclohexanol and Cyclohexanone by Gas-Phase Photocatalytic Oxidation? -- 7.4 Photocatalytic Membrane Reactors -- 7.5 Concluding Remarks -- References -- Chapter 8: Solar Light Active Nano-photocatalysts -- 8.1 Introduction -- 8.2 Mechanism of Semiconductor-Mediated Photocatalysis -- 8.2.1 Nano-TiO2 as Photocatalysts -- 8.2.2 Nano-ZnO as Photocatalysts -- 8.2.3 Graphitic Carbon Nitride as Photocatalysts -- 8.2.4 Titanates as Photocatalysts -- 8.2.5 Nano-metal Sulphides as Photocatalysts -- 8.3 Strategies for Making Solar/Visible Light Active Photocatalysts -- 8.3.1 Metal/Non-metal Doping -- 8.3.2 Addition of Photosensitive Materials -- 8.3.3 Construction of Heterojunctions/Composites -- 8.3.4 Construction of Nanohybrid Materials -- 8.3.5 Surface Modification -- 8.4 Conclusion -- References -- Chapter 9: High-Performance Photocatalysts for Organic Reactions -- 9.1 Introduction -- 9.2 Photocatalytic Oxidation of Alcohols -- 9.3 Selective Oxidation and Oxidative Coupling of Amines -- 9.4 Photocatalytic Cyanation -- 9.5 Photocatalytic Cycloaddition and C-C Bond Formation Reactions -- 9.6 Miscellaneous Reactions -- 9.7 Outlook -- 9.8 Conclusion -- References -- Index.

Anmerkung: Intro -- Preface -- Contents -- 1 Separation and Purification of Amino Acids -- 1.1 Introduction -- 1.2 Ion Exchange Chromatography in the Separation of Amino Acids -- 1.3 Ion Exchange Chromatography of Amino Acids -- 1.4 Ion Exchange Resins -- 1.5 Buffer Systems in IEC for Separation of Amino Acids -- 1.5.1 Sodium Citrate Buffer System -- 1.5.2 Lithium Citrate Buffer System -- 1.6 The Relation Between the Concentration of Eluent and Retention Time of Amino Acids -- 1.7 Effect of Temperature on Separation of Amino Acids -- 1.8 Effect of pH on Separation of Amino Acids -- 1.9 Effect of the Flow Rate of the Eluting Buffer on the IEC of Amino Acids -- 1.10 Regeneration of the Ion Exchange Column -- 1.11 Conclusion -- References -- 2 Ion Exchange Chromatography for Enzyme Immobilization -- 2.1 Introduction -- 2.2 Enzyme Immobilization -- 2.2.1 Immobilization Approaches -- 2.3 Ion-Exchange as an Immobilization Tool -- 2.4 Enzyme Immobilization Research and Application by Ion-Exchange in the Laboratory and Industry -- 2.5 Conclusion and Future Prospects -- References -- 3 Determination of Morphine in Urine -- 3.1 Introduction -- 3.1.1 Structural Features of Morphine -- 3.1.2 Physical Properties -- 3.1.3 Various Routes of Morphine Administration -- 3.1.4 Stay Period of Morphine in the Body -- 3.2 What Is Drug Abuse? -- 3.2.1 Fatal Dose of Morphine -- 3.2.2 Statistics Towards Morphine Addiction -- 3.2.3 Adverse Effect of Morphine -- 3.3 Samples Used for Detection of Morphine -- 3.3.1 Sample Collection/Preparation Prior to Detection -- 3.3.2 Extraction and Derivatization -- 3.4 Detection of Morphine in Urine -- 3.4.1 Chromatographic Methods -- 3.4.2 Liquid Chromatography (LC) and High-Performance Liquid Chromatography (HPLC) -- 3.4.3 Thin-Layer Chromatography (TLC) -- 3.4.4 Capillary Electrophoresis (CE) -- 3.4.5 Electrochemical Detection. , 3.4.6 Combination of Molecularly Imprinted Polymer with Chromatography -- 3.4.7 Some Miscellaneous Detection Techniques -- 3.5 Conclusion and Future Scope -- References -- 4 Chromatographic Separation of Amino Acids -- 4.1 Introduction -- 4.1.1 History -- 4.1.2 Classification of Amino Acids -- 4.2 Separation -- 4.2.1 What is Separation? -- 4.2.2 Why Need to Do Separation of Amino Acids? -- 4.2.3 What is Chromatography? -- 4.2.4 Classification of Chromatographic Methods -- 4.2.5 Advantages of Chromatographic Methods Over Other Methods -- 4.3 Separation of Amino Acids by Gas Chromatography (GC) -- 4.4 Liquid Chromatography (LC) -- 4.4.1 Separation of Amino Acids by High-Performance Liquid Chromatography (HPLC) -- 4.4.2 Advantages of Liquid Chromatography Over the Gas Chromatography -- 4.5 Amino Acid Separation by Countercurrent Chromatography (CCC) -- 4.6 Separation of Amino Acids by Thin-Layer Chromatography (TLC) -- 4.6.1 Preparation of Thin Plates -- 4.6.2 Sample Spotting on the Thin-Layer Plate -- 4.6.3 Detection of Amino Acids on the Thin-Layer Plate -- 4.7 Separation of Amino Acids by Capillary Electrophoresis (CE) -- 4.7.1 Various Modes for Capillary Electrophoresis (CE) -- 4.8 Separation of Amino Acids by the Hyphenated Technique -- 4.8.1 List of Hyphenated Techniques -- 4.8.2 Separation of Amino Acids Using GC-MS -- 4.8.3 Separation of Amino Acids by LC-MS -- 4.8.4 Separation of Amino Acids by LC-MS-MS -- 4.8.5 Separation of Amino Acids by CE-MS -- 4.9 Conclusion and Future Scope -- References -- 5 Applications of Ion-Exchange Chromatography in Pharmaceutical Analysis -- 5.1 Introduction -- 5.2 Application of Ion-Exchange Chromatography in Quantitative Analysis -- 5.2.1 Single-Mode Ion-Exchange Chromatography -- 5.2.2 Analysis of Small Molecules (Organic and Inorganic Ions) -- 5.2.3 Mixed-Mode Chromatography. , 5.3 Pretreatment and Separation Prior to Analysis -- 5.3.1 Ionic Solid-Phase Extraction -- 5.3.2 Mixed-Mode Ion-Exchange Solid-Phase Extraction -- 5.3.3 Flow Injection Ion-Exchange Preconcentration -- 5.4 Summary -- References -- 6 Thermodynamic Kinetics and Sorption of Bovine Serum Albumin with Different Clay Materials -- 6.1 Introduction -- 6.2 Experimental -- 6.3 Results and Discussion -- 6.3.1 The Effect of Some Specific Physicochemical Properties BSA onto Adsorption -- 6.3.2 Analyses of FTIR, TGA, and SEM Images -- 6.3.3 Kinetic Analysis -- 6.3.4 Thermodynamic Parameters -- 6.4 Conclusions -- References -- 7 Sorbitol Demineralization by Ion Exchange -- 7.1 Introduction -- 7.2 Industrial Application of Sorbitol -- 7.3 Importance of Demineralization/Deashing of Sorbitol -- 7.4 Role of Ion-Exchange Chromatography -- 7.5 Different Types of Ion Exchangers for Sorbitol Demineralization -- 7.5.1 Cation-Exchange Chromatography -- 7.5.2 Anion-Exchange Chromatography -- 7.6 Conclusion -- References -- 8 Separation and Purification of Nucleotides, Nucleosides, Purine and Pyrimidine Bases by Ion Exchange -- 8.1 Introduction -- 8.2 Ion-Exchange Chromatography -- 8.2.1 Mechanism of Ion Exchange -- 8.2.2 Components of Ion-Exchange Chromatography -- 8.3 Nucleotides -- 8.4 Nucleosides -- 8.5 Purines and Pyrimidines -- 8.6 Column Preparation and Operation -- 8.7 Operation -- 8.8 Impact of Separation Parameters -- 8.9 Separation of Nucleotides -- 8.9.1 Fractionation of Nucleotides -- 8.9.2 Cation-Exchange Resin -- 8.9.3 Anion-Exchange Materials -- 8.10 Separation of Nucleosides -- 8.10.1 Purification of Nucleosides -- 8.10.2 Cation-Exchange Chromatography -- 8.10.3 Anion-Exchange Chromatography -- 8.11 Separation of Purines and Pyrimidines -- 8.11.1 Cation-Exchange Chromatography -- 8.11.2 Anion-Exchange Chromatography. , 8.12 Applications of Ion-Exchange Chromatography -- 8.13 Conclusion -- References -- 9 Separation and Purification of Vitamins: Vitamins B1, B2, B6, C and K1 -- 9.1 Introduction -- 9.2 Significance of Vitamins -- 9.3 Classification of Vitamins -- 9.3.1 Water-Soluble Vitamins -- 9.3.2 Fat-Soluble Vitamins -- 9.4 Sources of Vitamins -- 9.4.1 B Vitamins -- 9.4.2 Vitamin C -- 9.4.3 Vitamin K -- 9.5 Vitamin Deficiency Disorders -- 9.6 B Vitamins -- 9.6.1 Vitamin B1 -- 9.6.2 Vitamin B2 -- 9.6.3 Vitamin B6 -- 9.7 Vitamin C -- 9.8 Vitamin K1 -- 9.9 Separation and Purification of Vitamin -- 9.10 Ion-Exchange Chromatography -- 9.11 Mechanism of Ion-Exchange Chromatography -- 9.12 Separation and Purification of Vitamins B1, B2 and B6 -- 9.13 Separation and Purification of Vitamin C -- 9.14 Ion-Exchange Separation and Purification of Vitamin K1 -- 9.15 Conclusion -- References -- 10 Colour Removal from Sugar Syrups -- 10.1 Colourants in Sugar Solutions -- 10.1.1 Determination of Colour in Sugar and Sugar Juices -- 10.1.2 Colour Substances in Sugar and Sugar Solutions -- 10.1.3 Formation of Beet and Cane Colourants During the Technological Process -- 10.1.4 Removal of Colourants from Beet and Cane Sugar and Sugar Solution -- 10.2 Decolourisation with Ion-Exchange Resins -- 10.2.1 The Terminology Used in Ion-Exchange Technology -- 10.2.2 Types of Ion-Exchange Resins -- 10.2.3 Set-up of Industrial Chromatographic Systems for Colour Removal -- 10.2.4 Comparison of Ion-Exchange Technology with Other Decolourising Techniques -- References.

Anmerkung: Intro -- Preface -- Contents -- Chapter 1: Introduction to Carbon Dioxide Capture and Storage -- 1.1 Introduction -- 1.2 Carbon Dioxide -- 1.3 Carbon Dioxide Capture and Storage Technology -- 1.3.1 Capturing and Separation -- 1.3.2 Transport -- 1.3.3 Injection and Storage -- 1.3.3.1 Integrity Issues -- 1.3.4 Monitoring -- 1.4 Technological and Scientific Concerns -- 1.5 Summary -- References -- Chapter 2: Sources of Carbon Dioxide and Environmental Issues -- 2.1 Introduction -- 2.2 Source of Carbon Dioxide -- 2.2.1 Anthropogenic Activities -- 2.2.1.1 Carbon Dioxide Emissions from Fossil Fuels´ Combustion -- 2.2.1.2 Trends in emissions -- 2.2.1.3 Industrial Emissions -- 2.2.1.4 Overpopulation and Carbon Dioxide Emissions -- 2.2.1.5 Agriculture Sector -- 2.2.2 Natural Sources of Carbon Dioxide -- 2.2.2.1 Forest Fires -- 2.2.2.2 Volcanic eruption -- 2.3 Environmental Issues Related to Carbon Dioxide Emissions -- 2.3.1 Cyclones and Hurricanes -- 2.3.2 Droughts -- 2.3.3 Heat Waves -- 2.3.4 Food System and Food Security -- 2.3.5 Glaciers Melting -- 2.4 Conclusion -- References -- Chapter 3: Carbon Capture Utilization and Storage Supply Chain: Analysis, Modeling and Optimization -- 3.1 Introduction -- 3.2 Status of Carbon Capture Utilization and Storage Supply Chain -- 3.3 Carbon Capture Utilization and Storage Technology Overview -- 3.3.1 CO2 Capture Options -- 3.3.1.1 Absorption Technology -- 3.3.1.2 Adsorption Technology -- 3.3.1.3 Membrane Technology -- 3.3.1.4 Chemical Looping Combustion -- 3.3.1.5 Cryogenic Technology -- 3.3.1.6 Hybrid Technology -- 3.3.2 CO2 Utilization Options -- 3.3.3 CO2 Storage Options -- 3.4 Design and Optimization of Carbon Capture Utilization and Storage Supply Chain -- 3.4.1 Methodology for the Design -- 3.4.2 Development of Optimization Tool -- 3.5 Cost Analysis. , 3.6 Literature Work About Carbon Capture Utilization and Storage Supply Chain -- 3.7 Conclusions -- References -- Chapter 4: Natural Carbon Sequestration by Forestry -- 4.1 Introduction -- 4.2 Influence of the Environment and Climate Variables in the Global Carbon Cycle -- 4.2.1 Nitrogen Fertilisation -- 4.2.2 Temperature and Soil Water Availability -- 4.2.3 Radiation -- 4.2.4 Climate Extremes and Disturbance -- 4.3 Forests Global Carbon Sink -- References -- Chapter 5: Carbon Sequestration via Biomineralization: Processes, Applications and Future Directions -- 5.1 Introduction -- 5.2 Biomineralization Processes and Mechanisms -- 5.2.1 Microbially-Mediated Biomineralization -- 5.2.2 Plant-Mediated Biomineralization -- 5.3 Carbon Dioxide Sequestration -- 5.3.1 Microbially-Mediated Biomineralization -- 5.3.2 Plant-Mediated Biomineralization -- 5.3.2.1 The Case of the Iroko Tree -- 5.3.2.2 The Case of Australian Acacia Species -- 5.3.2.3 Carbon Occlusion in Biominerals -- 5.4 Knowledge Gaps and Future Directions -- 5.5 Summary and Conclusions -- References -- Chapter 6: A Review of Coupled Geo-Chemo-Mechanical Impacts of CO2-Shale Interaction on Enhanced Shale Gas Recovery -- 6.1 Introduction -- 6.2 Properties of Shale and CO2 -- 6.2.1 Shale -- 6.2.2 CO2/Supercritical CO2 -- 6.3 Interaction of CO2 and Shale -- 6.3.1 Interaction of Shale with Anhydrous CO2 -- 6.3.2 CO2-Water-Rock Geochemical Reactions in Shale -- 6.3.3 CO2 Adsorption Induced Swelling in Shale -- 6.4 Effect of CO2-Shale Interaction on Rock Properties -- 6.4.1 Porosity and Permeability -- 6.4.2 Mechanical Properties -- 6.4.3 Adsorption Properties -- 6.5 Effect of CO2-Shale Interaction on Groundwater Quality -- 6.6 Conclusions -- References -- Chapter 7: Plantation Methods and Restoration Techniques for Enhanced Blue Carbon Sequestration by Mangroves -- 7.1 Introduction. , 7.2 Blue Carbon Sequestration -- 7.2.1 Carbon Balance in a Mangrove Ecosystem -- 7.3 Plantation Techniques for Mangroves -- 7.3.1 Establishment of Mangrove Nursery -- 7.3.2 Transplantation of Nursery Grown Seedlings -- 7.3.3 Direct Seeding Method -- 7.3.4 Drain and Trench Method -- 7.3.5 Fish Bone Canal System -- 7.4 Post Plantation Management -- 7.5 Community Participation in Mangrove Plantation -- 7.6 Conclusion -- References -- Chapter 8: Biowaste for Carbon Sequestration -- 8.1 Introduction -- 8.2 Sources of Biowastes -- 8.3 Environmental Impact of Biowastes -- 8.4 Application of Biowastes for Carbon Sequestration -- 8.4.1 Composting Technology -- 8.4.2 As a Fertilizer/Organic Farming -- 8.4.3 Energy -- 8.4.4 Biochar Technology -- 8.5 Future Research Directions -- 8.6 Conclusion -- References -- Index.