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  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Green chemistry. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (299 pages)
    Edition: 1st ed.
    ISBN: 9783030678845
    Series Statement: Advances in Science, Technology and Innovation Series
    DDC: 660.0286
    Language: English
    Note: 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.
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  • 2
    Online Resource
    Online Resource
    Singapore :Springer Singapore Pte. Limited,
    Keywords: Botanical chemistry. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (318 pages)
    Edition: 1st ed.
    ISBN: 9789811566073
    Series Statement: Environmental and Microbial Biotechnology Series
    DDC: 579
    Language: English
    Note: Intro -- Preface -- Contents -- 1: Application of Microbial Biosurfactants in the Food Industry -- 1.1 Surfactants in the Food Industry -- 1.1.1 Food Additives -- 1.1.2 Biosurfactants as Food Preservatives -- 1.1.2.1 Emulsifying Agents -- 1.1.2.2 Antibiofilm Agents -- 1.1.2.3 Antimicrobial Agents -- 1.1.2.4 Antioxidant Agents -- 1.1.3 Industrial Prospects -- References -- 2: Microbial Biosurfactants for Contamination of Food Processing -- 2.1 Introduction -- 2.1.1 Food Contamination -- 2.1.2 Contamination in Food Processing -- 2.2 Microbial Biosurfactants Use in Food Processing -- 2.2.1 Glycolipids -- 2.2.2 Lipopeptides -- 2.3 Application of Microbial Surfactants in Food Processing -- 2.3.1 Biofilm Control -- 2.3.2 Food Preservatives -- 2.4 Concluding Remarks -- References -- 3: Antioxidant Biosurfactants -- 3.1 Introduction -- 3.2 Sources of Biosurfactants -- 3.2.1 Plant-Based Biosurfactants -- 3.2.1.1 Saponins -- Structure, Properties, and Types of Saponins -- Saponins as a Biosurfactants -- 3.2.2 Microbe-Based Biosurfactants -- 3.2.2.1 Types of Microbial Surfactants -- Glycolipids -- Rhamnolipids -- Sophorolipids -- Trehalolipids -- Succinoyl Trehalolipids -- Cellobiose Lipids -- Mannosylerythritol Lipids -- Xylolipids -- Mannose Lipids -- Lipopeptides or Lipoprotein -- Bacillus-Related Lipopeptides -- Surfactin -- Fengycin -- Iturin -- Kurstakins -- Lichenysins -- Pseudomonas-Related Lipopeptides -- Actinomycetes-Related lipopeptides -- Fungal-Related Lipopeptides -- Phospholipids, Fatty Acids (Mycolic Acids), and Neutral Lipids -- Polymeric Surfactants -- Particulate Surfactants -- 3.3 Factors Affecting Biosurfactant Production -- 3.3.1 pH and Temperature -- 3.3.2 Aeration and Agitation -- 3.3.3 Effect of Salt Salinity -- 3.3.4 Optimization of Cultivation Medium -- 3.3.4.1 Effect of Carbon Source -- 3.3.4.2 Effect of Nitrogen Source. , 3.3.4.3 Effect of Carbon to Nitrogen (C/N) Ratio -- 3.4 Screening of Microorganisms for Biosurfactant Production -- 3.4.1 Oil Spreading Assay -- 3.4.2 Drop Collapse Assay -- 3.4.3 Blood Agar Method/Hemolysis Assay -- 3.4.4 Hydrocarbon Overlay Agar -- 3.4.5 Bacterial Adhesion to Hydrocarbon (BATH) Assay -- 3.4.6 CTAB Agar Plate Method/Blue Agar Assay -- 3.4.7 Phenol: Sulfuric Acid Method -- 3.4.8 Microplate Assay -- 3.4.9 Penetration Assay -- 3.4.10 Surface/Interface Activity -- 3.4.11 Emulsification Activity -- 3.5 Antioxidant Properties of Biosurfactant -- 3.6 Conclusion -- References -- 4: Classification and Production of Microbial Surfactants -- 4.1 Introduction -- 4.1.1 Global Biosurfactant Market -- 4.2 Types of Biosurfactants -- 4.2.1 Glycolipids -- 4.2.1.1 Rhamnolipids -- 4.2.1.2 Sophorolipids -- 4.2.1.3 Trehalolipids -- 4.2.2 Lipoproteins and Lipopeptides -- 4.2.3 Fatty Acids -- 4.2.4 Phospholipids -- 4.2.5 Polymeric Biosurfactants -- 4.3 Factors Influencing Biosurfactant Productivity -- 4.3.1 Nutritional Factors -- 4.3.1.1 Carbon Source -- 4.3.1.2 Low-Cost and Waste Substrates -- 4.3.1.3 Nitrogen Source -- 4.3.1.4 Minerals -- 4.3.2 Environmental Factors -- 4.3.3 Cultivation Strategy -- 4.3.3.1 Solid-State Fermentation (SSF) -- 4.3.3.2 Submerged Fermentations (SmF) -- References -- 5: Microbial Biosurfactants and Their Potential Applications: An Overview -- 5.1 Introduction -- 5.2 Classes of Biosurfactants -- 5.2.1 Glycolipids -- 5.2.2 Lipopolysaccharides -- 5.2.3 Lipopeptides and Lipoproteins -- 5.2.4 Phospholipids -- 5.2.5 Fatty Acids -- 5.3 Microbial Production of Biosurfactants -- 5.4 Genes Involved in the Production of Microbial Biosurfactants -- 5.5 Applications -- 5.5.1 In Petroleum Industry -- 5.5.1.1 Mechanism of MEOR -- 5.5.2 Biosurfactant-Mediated Bioremediation -- 5.5.3 In Food Industry -- 5.5.4 In Agriculture. , 5.5.5 In Cosmetics -- 5.5.6 Biosurfactant in Nanotechnology -- 5.5.7 Biosurfactants as Drug Delivery Agents -- 5.5.8 Antimicrobial Activity of Biosurfactants -- 5.5.9 Biosurfactant as Anti-Adhesive Agent -- 5.5.10 In Fabric Washing -- 5.6 Conclusions -- References -- 6: Biodegradation of Hydrophobic Polycyclic Aromatic Hydrocarbons -- 6.1 Introduction -- 6.2 Health Related to PAHs -- 6.2.1 Consequences of Consistent of PAH Exposure by Human -- 6.2.2 Problems Associated with PAHs Via Cytochrome P450 -- 6.3 Biodegradation of PAHs -- 6.3.1 Challenges of Limited Aqueous Solubility in Water -- 6.3.2 Biodegradation Pathway of PAHs -- 6.3.2.1 Naphthalene -- 6.3.2.2 Pyrene -- 6.3.2.3 Fluoranthene -- 6.4 Biosurfactants -- 6.4.1 Biosurfactants -- 6.4.1.1 Glycolipid -- Rhamnolipids -- Cellobiose Lipids -- Sophorolipids -- Trehalolipids -- Mannosylerythritol Lipid -- 6.4.1.2 Lipopeptides -- 6.4.1.3 Phospholipids -- 6.4.2 Polymeric Biosurfactants -- 6.5 Enhanced Biodegradation of PAHs by Biosurfactant -- 6.5.1 Biodegradation in Micelles -- 6.5.2 Biosurfactant Acting as Bioemulsifier -- 6.6 Conclusions -- References -- 7: Surfactin: A Biosurfactant Against Breast Cancer -- 7.1 Introduction -- 7.2 Biosurfactants and Its Types -- 7.2.1 Glycolipids -- 7.2.1.1 Rhamnolipids -- 7.2.1.2 Sophorolipids -- 7.2.1.3 Trehalolipids -- 7.2.2 Lipopeptides -- 7.2.3 Fatty Acids -- 7.2.4 Phospholipids -- 7.2.5 Polymeric Biosurfactant -- 7.3 Surfactin: Structure, Membrane Interaction, Biosynthesis, and Regulation -- 7.3.1 Structure -- 7.3.2 Membrane Interaction -- 7.3.3 Biosynthesis -- 7.3.4 Regulation -- 7.4 Surfactin and Breast Cancer -- 7.5 Conclusion -- References -- 8: Anti-Cancer Biosurfactants -- 8.1 Introduction -- 8.2 Biosurfactants Classification and Structure -- 8.2.1 Mannosylerythritol Lipids (MELs) -- 8.2.2 Succinoyl Trehalose Lipids (STLs) -- 8.2.3 Sophorolipids. , 8.2.4 Rhamnolipids (RLs) -- 8.2.5 Myrmekiosides -- 8.2.6 Cyclic Lipopeptides (CLPs) -- 8.2.6.1 Amphisin, Tolaasin, and Syringomycin CLPs -- 8.2.6.2 Iturin and fengycin CLPs -- 8.2.6.3 Surfactin CLP -- 8.2.7 Rakicidns and Apratoxins -- 8.2.8 Serrawettins -- 8.2.9 Monoolein -- 8.2.10 Fellutamides -- 8.3 Biosurfactants Production -- 8.3.1 Factors Involved in Biosurfactants Production -- 8.3.1.1 Source of Carbon -- 8.3.1.2 Source of Nitrogen -- 8.3.1.3 Effect of Ions -- 8.3.1.4 Physical Factors -- 8.4 Anti-Cancer Activity of Biosurfactants -- 8.4.1 Breast Cancer -- 8.4.2 Lung Cancer -- 8.4.3 Leukemia -- 8.4.4 Melanoma -- 8.4.5 Colon Cancer -- 8.5 Biosurfactants as Drug Delivery System (DDS) -- 8.5.1 Liposomes -- 8.5.2 Niosomes -- 8.5.3 Nanoparticles -- 8.6 Conclusions and Future Challenges -- References -- 9: Biosurfactants for Oil Pollution Remediation -- 9.1 Introduction -- 9.2 Oil Pollution and Its Remediation -- 9.2.1 Oil Pollution -- 9.2.2 Oil Remediation in Polluted Environments -- 9.3 Biosurfactants -- 9.3.1 Synthesis of Biosurfactants -- 9.3.2 Biosurfactant Role in Oil Degradation -- 9.4 Application of Biosurfactants Used for Oil Remediation -- 9.4.1 Oil-Polluted Soil Bioremediation -- 9.4.2 Bioremediation of Marine Oil Spills and Petroleum Contamination -- 9.4.3 Cleaning of Oil Tanks and Pipelines -- 9.4.4 Bioremediation of Heavy Metals and Toxic Pollutants -- 9.5 Conclusion -- References -- 10: Potential Applications of Anti-Adhesive Biosurfactants -- 10.1 Introduction -- 10.2 Biosurfactants That Display Anti-Adhesive Activity -- 10.3 Biofilms and the Adhesion Process: Mechanisms and Effects -- 10.4 Applications of Biosurfactants as Anti-Adhesive Agents -- 10.4.1 Anti-Adhesive Applications in the Biomedical Field -- 10.4.2 Anti-Adhesive Applications in the Food Industry Surfaces -- 10.5 Future Trends and Conclusions -- References. , 11: Applications of Biosurfactant for Microbial Bioenergy/Value-Added Bio-Metabolite Recovery from Waste Activated Sludge -- 11.1 Introduction -- 11.2 Applications of Surfactants for Value-Added Bio-Metabolites Recovery from WAS -- 11.3 Applications of Surfactants for Energy Recovery from WAS -- 11.4 Applications of Surfactants for Refractory Organic Decontamination from WAS -- 11.4.1 PAHs Decontamination -- 11.4.2 Dye Decontamination -- 11.4.3 PCB Decontamination -- 11.5 Applications of Surfactants for WAS Dewatering -- 11.6 Applications of Surfactants for Heavy Metal Removal from WAS -- 11.7 State-of-the-Art Processes to Promote Organics Biotransformation from WAS -- 11.7.1 Co-Pretreatment -- 11.7.2 Interfacing AD with Bioelectrochemical Systems -- 11.7.3 Optimizing Process Conditions -- 11.8 Conclusion -- References -- 12: Application of Microbial Biosurfactants in the Pharmaceutical Industry -- 12.1 Introduction -- 12.2 Mechanism of Interaction of Biosurfactants -- 12.3 Physiochemical Properties -- 12.3.1 Surface Tension -- 12.3.2 Biosurfactant and Self-Assembly -- 12.3.3 Emulsification Activity -- 12.4 Application of Biosurfactants in Pharmaceutical Industry -- 12.4.1 Biosurfactant as an Antitumor/AntiCancer Agent -- 12.4.2 Biosurfactants as Drug Delivery Agents -- 12.4.3 Wound Healing and Dermatological Applications -- 12.4.4 Potential Antimicrobial Application -- 12.4.5 Other Applications in the Pharmaceutical Field -- 12.5 Applications of Surfactin in Pharmaceutical Industry -- 12.6 Concluding Remarks -- References -- 13: Antibacterial Biosurfactants -- 13.1 Introduction -- 13.2 Glycolipids -- 13.2.1 Rhamnolipids -- 13.2.2 Sophorolipids -- 13.2.3 Trehalose Lipids -- 13.3 Lipopeptides -- 13.4 Phospholipids -- 13.5 Antibacterial Activity -- 13.6 Polymeric Surfactants -- 13.7 Fatty Acids -- 13.7.1 Bio-Sources of Fatty Acids. , 13.7.2 Role of Fatty Acids as Antimicrobials.
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  • 3
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Renewable energy sources. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (354 pages)
    Edition: 1st ed.
    ISBN: 9783030728779
    Series Statement: Advances in Science, Technology and Innovation Series
    DDC: 628.532
    Language: English
    Note: 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.
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  • 4
    Online Resource
    Online Resource
    Millersville :Materials Research Forum LLC,
    Keywords: Electronic books.
    Description / Table of Contents: This book is intended to present the latest applicational advancements of MXenes in diversified sectors.
    Type of Medium: Online Resource
    Pages: 1 online resource (123 pages)
    Edition: 1st ed.
    ISBN: 9781644902875
    Series Statement: Materials Research Proceedings Series ; v.155
    Language: English
    Note: Intro -- front-matter -- Table of Contents -- Preface -- 1 -- Applications of MXenes in Supercapacitors -- 1. Introduction -- 2. Brief idea of MAX phase and MXene -- 3. MXene and MXene-based composites as supercapacitor electrode materials -- 4. Parameters that affect the electrochemical behaviors of MXene -- 4.1 Etchant -- 4.2 Etchant concentration -- 4.3 Surface termination group -- 4.4 Partial etching of 'A' group from the MAX phase -- 4.5 Etching time and etching temperature -- 5. Different types of supercapacitors with MXene -- 5.1 MXene-based symmetric supercapacitor -- 5.1.1 One-dimensional (1D) supercapacitor -- 5.1.2 Two-dimensional (2D) supercapacitor -- 5.1.3 Three-dimensional (3D) supercapacitor -- 5.2 MXene-based asymmetric supercapacitor -- 5.3 Current MXene based micro-supercapacitor -- 5.4 MXene-based transparent supercapacitor -- Conclusion -- References -- 2 -- Applications of MXenes in EMI shielding -- 2. Electromagnetic interference shielding mechanism -- 3. MXene for EMI shielding -- 3.1 Recent progress in EMI shielding performance of different MXenes composites -- Conclusion -- Acknowledgments -- References -- 3 -- MXenes for Nanophotonics -- 1. MXenes -An introduction and as a 2D Material -- 2. Types of MXene -- 3. Non-linear optical behavior of MXene -- 3.1 , - ., - ., - . MXene -- 3.2 , - ., - . MXene -- 3.2.1 Synthesis of , - ., - . MXene -- 3.2.2 Characterization Results -- 4. Optical and Electronic Trends -- 4.1 Optical Properties -- 4.2 Electronic properties -- 5. Theoretical outcomes -- 6. Experimental outcomes -- 7. Device implementation -- 7.1 Saturable absorber -- 7.2 Photodetectors based on MXene -- 7.3 Light emitting diodes -- 7.4 Photovoltaic devices -- 8. Future perspectives and challenges -- Conclusion -- References -- 4 -- Application of MXenes in Photodetectors -- 1. Introduction. , 2. Preparation techniques of MXenes -- 2.1 Etching (HF etching) method -- 2.2 Non-HF etching methods -- 2.3 Hydrothermal method -- 3. Properties of MXenes -- 3.1 Mechanical properties -- 3.2 Structural properties -- 3.3 Electronic properties -- 3.4 Optical properties -- 4. Application of MXenes in the field of photodetectors -- Conclusion -- Acknowledgments -- References -- 5 -- Applications of MXenes in Electrocatalysis -- 1. Introduction -- 1.1 Features of MXene as an Electrocatalyst -- 1.2 Mechanical properties of MXENE -- 1.3 Electrical structures of MXenes -- 2. Synthesis of MXenes -- 3. Applications of MXene as electrocatalyst -- 3.1 MXene for hydrogen evolution reaction -- 3.2 MXene for nitrogen reduction reaction -- 3.2 MXene for carbon dioxide reduction reaction -- 3.4 MXene for environmental remediation -- 3.5 MXene-based electrocatalysts for ORR -- 3.6 MXene for batteries storage and supercapacitors -- Conclusion -- Acknowledgments -- References -- back-matter -- Keyword Index -- About the Editors.
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  • 5
    Keywords: Organic compounds-Synthesis. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (590 pages)
    Edition: 1st ed.
    ISBN: 9780323996440
    DDC: 620.1180286
    Language: English
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  • 6
    Keywords: Environmental chemistry ; Environmental Chemistry ; Catalysis ; Pollution prevention ; Analytical chemistry ; Electrochemistry
    Description / Table of Contents: Preface -- 1. Use of carbon dioxide in polymer synthesis (Annalisa Abdel Azim, Alessandro Cordara, Beatrice Battaglino, Angela Re) -- 2. Biological conversion of carbon dioxide into volatile organic compounds (Ihana Aguiar Severo, Pricila Nass Pinheiro, Karem Rodrigues Vieira, Leila Queiroz Zepka, Eduardo Jacob-Lopes) -- 3. Application of metal organic frameworks in carbon dioxide conversion to methanol (Tamer Zaki) -- 4. Conversion of Carbon Dioxide into Formic Acid (Umesh Fegade and Ganesh Jethave) -- 5. Selective hydrogenation of carbon dioxide into methanol (Pham Minh, Roger, Parkhomenko, L'Hospital, Rego de Vasconcelos, Ro, Mahajan, Chen, Singh, N. Vo) -- 6. Conversion of carbon dioxide into formaldehyde (Trinh Duy Nguyen, Thuan Van Tran, Sharanjit Singh, Pham T. T. Phuong, Long Giang Bach, Sonil Nanda, Dai-Viet N. Vo) -- 7. A Short Review on Production of Syngas via Glycerol Dry Reforming (Sumaiya Zainal Abidin, Asmida Ideris, Nurul Ainirazali, Mazni Ismail)
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (XI, 202 p. 45 illus., 28 illus. in color)
    Edition: 1st ed. 2020
    ISBN: 9783030286385
    Series Statement: Environmental Chemistry for a Sustainable World 41
    Language: English
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  • 7
    Keywords: Environmental Medicine ; Environmental pollution ; Analytical biochemistry ; Environmental chemistry ; Environmental Chemistry ; Environmental health. ; Water pollution. ; Analytical chemistry.
    Description / Table of Contents: 1. Role of nano-photocatalysis in heavy metal detoxification -- 2. Solar photocatalysis applications to antibiotic degradation in aquatic systems -- 3. Biomass-based photocatalysts for environmental applications -- 4. Role of nano-photocatalysis in heavy metal detoxification -- 5. Phosphors-based photocatalysts for wastewater treatment -- 6. Nanocarbons and Polymers Supported TiO2 Nanostructures as Efficient Photocatalysts for Remediation of Contaminated -- 7. Wastewater and Hydrogen Production -- 8. Investigation in sono-photocatalysis process using doped-catalyst and ferrite nanoparticles for wastewater treatment -- 9. Magnetic-based photocatalyst for antibacterial application and catalytic performance -- 10. Antimicrobial activities of photocatalysts to water disinfection -- 11. Medicinal Applications of Photocatalysts
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (XIII, 269 p. 68 illus., 32 illus. in color)
    Edition: 1st ed. 2020
    ISBN: 9783030126193
    Series Statement: Environmental Chemistry for a Sustainable World 30
    Language: English
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  • 8
    Online Resource
    Online Resource
    Millersville, PA :Materials Research Forum LLC,
    Keywords: Electronic books.
    Description / Table of Contents: The book presents theoretical insights, characterization tools and mechanisms of green corrosion inhibitors.
    Type of Medium: Online Resource
    Pages: 1 online resource (242 pages)
    Edition: 1st ed.
    ISBN: 9781644901052
    Series Statement: Materials Research Foundations Series ; v.86
    Language: English
    Note: Intro -- front-matter -- Table of Contents -- Preface -- 1 -- Theoretical Insights in Green Corrosion Inhibitors -- 1. Introduction -- 2. Theoretical methods used in green corrosion inhibitors -- 2.1 Quantum chemistry methods -- 2.2 Quantitative structure-activity relationships -- 2.3 Molecular dynamics simulation -- 3. The progress of theoretical study in green corrosion inhibitors -- 3.1 The behavior of green corrosion inhibitor studied by combination of quantum chemistry and QSAR -- 3.1.1 Carbon steel inhibitors -- 3.1.2 Copper inhibitors -- 3.2 The performance of green corrosion inhibitor studied by combination of molecular simulation and quantum chemistry -- 3.2.1 Carbon steel inhibitor -- 3.2.2 Aluminum inhibitors -- 3.2.3 Copper inhibitors -- 3.3 The behavior of green corrosion inhibitor studied by combination of molecular simulation, quantum chemistry and QSAR -- 3.3.1 Carbon steel inhibitors -- 3.3.2 Copper inhibitors -- Conclusions -- Acknowledgments -- References -- 2 -- Effect of Natural Sources on the Corrosion Inhibition -- 1. Introduction -- 2. Green corrosion inhibitors -- 2.1 Protection of iron based surfaces via green corrosion inhibitors -- 2.1.1 Protection of iron surfaces via green corrosion inhibitors -- 2.1.2 Protection of mild steel surfaces via green corrosion inhibitors -- 2.1.3 Protection of steel surfaces via green corrosion inhibitors -- 2.1.4 Protection of carbon steel surfaces via green corrosion inhibitors -- 2.1.5 Protection of steel rebar surfaces via green corrosion inhibitors -- 2.2 Protection of aluminum surfaces via green corrosion inhibitors -- 2.3 Protection of copper surfaces via green corrosion inhibitors -- 2.4 Protection of tin surfaces via green corrosion inhibitors -- 2.5 Green corrosion inhibitors resources -- 3. Anti-corrosion mechanism (for natural inhibitors). , 3.1 Anodic, cathodic and mixed type inhibition -- 4. Corrosion inhibitors testing -- 5. Economic and industrial opportunities -- References -- 3 -- Green Inhibitors for Biocorrosion and Prevention -- 1. Introduction -- 1.1 The portability of the metal to the corrosion -- 1.2 The factors affecting the speed of corrosion -- 1.3 Types of corrosions -- 1.3.1 Pure chemical corrosion -- 1.3.2 Electrochemical corrosion -- 1.3.3 Homogeneous (general) corrosion -- 1.3.4 Local corrosion -- 1.3.5 Stress - corrosion cracking -- 1.3.6 Galvanic corrosion -- 1.3.7 Erosion corrosion (EC) -- 1.3.8 Crevice corrosion -- 1.3.9 Pitting corrosion (PC) -- 1.3.10 Exfoliation corrosion -- 1.3.11 Selective leaching -- 1.3.12 Nonmetallic corrosion -- 1.3 Corrosion of cement -- 1.5 Corrosion of organic materials -- 1.6 Environment factors -- 1.6.1 Effect of oxygen and oxidants -- 1.6.2 Effect of pH -- 1.6.2 Effect of anions and cations -- 1.7 Anti-corrosion methods -- 1.7.1 The green impediments for corrosion -- 1.7.2 Determination of green corrosion inhibitors based on ionic fluids -- 1.7.3 Corrosion suppressions from the biological waste -- Conclusion -- References -- 4 -- Electrochemical Studies of Green Corrosion Inhibitors -- 1. Introduction -- 2. Corrosion inhibitors -- 2.1 Green corrosion inhibitors -- 2.1.1 Natural products -- 2.1.2 Amino acids -- 2.1.3 Rare earth metal compounds -- 2.1.4 Recently used green inhibitors -- 3. Characterization techniques -- 3.1 Polarization methods -- 3.1.1 Linear polarization resistance method -- 3.1.2 Potentiodynamic-galvanodynamic polarization -- 3.1.3 Cyclic potentiodynamic polarization -- 3.1.4 Cyclic galvano-staircase polarization -- 3.1.5 Conversion of Icorr (from polarization methods) to corrosion rates -- 3.1.6 Limitations associated with polarization methods -- 3.2 Electrochemical impedance spectroscopy (EIS). , 3.2.1 Interpretation of results (Nyquist & -- Bode plots) -- 3.2.2 Equivalent circuits -- 3.3 Electrochemical Noise (EN) measurements -- 3.4 Electrochemical Quartz Crystal Microbalance (EQCM) -- Concluding remark -- References -- 5 -- Green Corrosion Inhibitors for Technological Applications -- 1. Introduction -- 2. Green corrosion inhibitors -- 3. Technological applications of green corrosion inhibitors -- 3.1 Oil and gas sector -- 3.2 Reinforced concrete -- 3.3 Acid pickling industry -- 3.4 Coatings -- 3.5 Aircraft industry -- 3.6 Water industry -- Conclusion -- Acknowledgment -- References -- 6 -- Pyrazine Derivatives as Green Corrosion Inhibitors -- 1. Introduction -- 2. Pyrazine and its derivative as prominent corrosion inhibitor for metals and alloys in corrosive media -- 3. Adsorption mechanism -- Further aspects -- Conclusion -- Abbreviations -- Acknowledgement -- References -- 7 -- Biological Corrosion Inhibitors for Concrete -- 1. Introduction -- 2. Biological Corrosion Inhibitors -- 2.1 Microbial -- 2.1.1 Bacterial -- 2.1.1.1 Ureolytic -- 2.1.1.2 Non-ureolytic -- 2.1.2 Nitrate reducing bacteria -- 2.1.3 Biomolecules -- 2.1.4 Deoxyribonucleic acid (DNA) -- 2.1.5 Mussel adhesive proteins -- 2.1.6 Fungus -- 2.2 Botanical -- 2.2.1 Extract of tree/plant leaves -- 2.2.2 Bark extract of trees/plants -- 2.2.3 Seeds or grains -- 2.2.4 Plant roots extracts -- 2.2.5 Plants mucilage -- 2.2.6 Algae -- 3. Comparison -- Conclusion -- References -- 8 -- Green Corrosion Inhibitor for Electronics -- 1. Introduction -- 2. Causes and factors for corrosion in electronics -- 2.1 Contaminant gases affect the manufacturing areas -- 2.2 Other problems faced in manufacturing process -- 2.3 Effects of ammonia -- 2.4 Effects of ozone, boron and other volatile organic compounds -- 2.5 Airborne contamination in various sector -- 2.5.1 Telecom industry. , 2.5.2 Distributed control system (DCS) -- 2.5.3 Data centers -- 3. Metals or specific alloys component for electronics -- 4. Electronic component susceptibility towards corrosion and failure analysis -- 4.1 Printed circuit board -- 4.2 Contact and connector -- 4.2.1 Pore corrosion in electrical contacts -- 4.2.2 Fretting corrosion of electronic connectors -- 4.3 Integrated circuits -- 4.4 Solder corrosion: the corrosive effect of soldering flux -- 4.5 Hermetic packages -- 5. Reliability and cleanliness -- 6. Electronics corrosion protection -- 7. Vapor phase corrosion inhibitor (VPCI) technology -- 8. Vapor pressure measurement by various methods -- 8.1 Regnault dynamic method -- 8.2 Boiling point determination method -- 8.3 Knudsen effusion method -- 8.4 Microbalance method -- 8.5 Torsion effusion method -- 9. Effect of temperature on the vapor pressure -- 10. Effect of pH -- 11. Types of vapor phase corrosion inhibitors (VPCI) -- 12. Analysis of corrosion by different method -- 12.1 Vapor pressure determination -- 12.2 Weight loss method -- 12.3 Esckhe method -- 12.4 Salt spray method -- 13. Advantages of VPCI -- References -- back-matter -- Keyword Index -- About the Editors.
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  • 9
    Online Resource
    Online Resource
    Millersville, PA :Materials Research Forum LLC,
    Keywords: Electronic books.
    Description / Table of Contents: The book presents an in-depth review of biomass-derived materials for energy storage technologies. Biomass is the most renewable and abundant carbon resource and has great potential for sustainable energy production.
    Type of Medium: Online Resource
    Pages: 1 online resource (151 pages)
    Edition: 1st ed.
    ISBN: 9781644900871
    Series Statement: Materials Research Foundations Series ; v.78
    Language: English
    Note: Intro -- front-matter -- Table of Contents -- Preface -- 1 -- Bone Char as a Support Material to Build a Microbial Biocapacitor -- 1. Introduction -- 2. Influence of the chemical and textural properties on biochar -- 3. Bioanode preparation -- 4. Accumulated charge -- 5. Biochar-based anode and bioanode capacitances -- Conclusions -- Acknowledgements -- List of abbreviations -- References -- 2 -- Nature Inspired Materials for Energy Storage -- 1. Introduction -- 2. Properties of nature-derived carbons properties for fulfilling the operational need for EDLC- supercapacitors -- 3. Various preparation mechanisms for nature derived carbons for supercapacitor -- 4. Advantages of naturally-derived carbons over graphene and CNT for EDLC supercapacitors -- 5. Use of different biological precursors -- 5.1 Plant-derived precursors -- 5.2 Fruit based precursors -- 5.3 Microbial-based precursors -- 5.4 Animal-based precursors -- 6. Structural characteristics and properties of nature derived carbons -- Conclusions and future directions -- References -- 3 -- Biomass Derived Composites for Energy Storage -- 1. Introduction -- 2. Sustainable biomass-carbon materials -- 3. Calculation paramaters -- 4. Biomass activation -- 4.1 Physical activation -- 4.2 Chemical activation -- 4.3 Hydrothermal carbonization -- 4.4 Other activations -- 5. Outlook -- Conclusions and prospects -- References -- 4 -- Lignin-Derived Materials for Energy Storage -- 1. Introduction -- 2. Lignin isolation process -- 3. Lignin carbon fibres -- 3.1 Activation techniques -- 3.2 Lignin- Lignin blends -- 3.3 Lignin-Cellulose blends -- 3.4 Fractionation -- 3.5 Reinforcement -- 3.6 Chemical modification -- 3.7 New lignin types -- 4. Lignin-derived porous carbon -- 5. Challenges with graphite-based electrodes -- 6. Lignin for electrochemical applications -- 6.1 Lithium-ion batteries. , 6.2 Electrochemical double layer capacitors -- 6.3 Electrochemical pseudocapacitors -- 6.4 Sodium -ion batteries -- 6.5 Lignin as binder -- Conclusion and Perspectives -- Acknowledgements -- This research work was financially supported by the University Malaya Impact-Oriented Interdisciplinary Research Grant (No.IIRG018A-2019) and Global Collaborative Programme - SATU Joint Research Scheme (No. ST012-2019). -- References -- 5 -- Bamboo Derived Materials for Energy Storage -- 1. Introduction -- 2. Fabrication of electrode material for supercapacitor application -- 3. Physical characterization -- 4. Electrochemical measurements -- Conclusion -- References -- 6 -- Cellulose-Derived Electrodes for Energy Storage -- 1. Introduction -- 2. Cellulose based flexible composite electrodes -- 3. Cellulose carbonization and activation -- 4. Cellulose-derived carbon for supercapacitors -- 5. Cellulose-derived carbon for high-frequency supercapacitors -- 6. Cellulose-derived carbon for lithium-ion batteries -- 7. Cellulose-derived carbon for lithium-sulfur batteries -- 8. Cellulose-derived carbon for other batteries -- Conclusion -- References -- back-matter -- Keyword Index -- About the Editors.
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  • 10
    Online Resource
    Online Resource
    Millersville, PA :Materials Research Forum LLC,
    Keywords: Electronic books.
    Description / Table of Contents: This book focuses on aerogels and their applications in such areas as energy storage, thermal storage, catalysis, water splitting and environmental remediation.
    Type of Medium: Online Resource
    Pages: 1 online resource (282 pages)
    Edition: 1st ed.
    ISBN: 9781644900994
    Series Statement: Materials Research Foundations Series ; v.84
    Language: English
    Note: Intro -- front-matter -- Table of Contents -- Preface -- 1 -- Nanocellulose Aerogels -- 1. Introduction -- 2. Production processes of nanocellulose aerogels -- 3. Properties of nanocellulose aerogels -- 4. Applications of nanocellulose aerogels -- 4.1 Materials absorbents -- 4.2 Gas filters and membranes -- 4.3 Packaging materials -- 4.4 Energy storage systems and electrical devices -- 4.5 Thermal insulation and fire-retardant materials -- 4.6 Pharmaceutical and biomedical applications -- 5. Final considerations -- References -- 2 -- Porous Aerogels -- 1. Porous aerogel history -- 2. Aerogel pore classification -- 3. Inorganic-silica based aerogels -- 3.1 Properties of silica-based aerogel -- 3.1.1 Texture -- 3.1.2 Thermal properties -- 3.1.3 Optical properties -- 3.1.4 Entrapment, release, sorption, and storage properties -- 4. Inorganic-nonsilicate aerogels -- 4.1 ZrO2 aerogels -- 4.1.1 ZrO2 aerogels in catalysis -- 4.1.2 ZrO2 aerogels in ceramics -- 4.1.3 ZrO2 aerogels in solid oxide fuel cells -- 4.2 TiO2 aerogels -- 5. Organic-natural/biogels -- 5.1 Polysaccharides aerogels -- 5.2 Chitosan aerogel -- 5.3 Pectin aerogel -- 5.4 Alginate aerogel -- 5.5 κ -Carrageenan aerogel -- 5.6 Starch aerogel -- 5.7 Curdlan aerogel -- 5.8 Cellulose aerogels -- 5.8.1 Cellulose aerogel monoliths -- 5.8.2 Nanostructured cellulose filaments in textile -- 6. Resorcinol-formaldehyde aerogels -- 7. Composite aerogels -- 7.1 Polymer-crosslinked aerogels -- 7.2 Effect of polymer addition on aerogel fragility -- 8. Exotic aerogels -- 8.1 Chalcogenide aerogels -- 8.1.1 Chalcogenide aerogels formation by thiolysis: GeS2 -- 8.1.2 Chalcogenide aerogels formation by cluster-linking -- 8.1.3 Chalcogenide aerogels formation by nanoparticle assembly -- 9. Conducting polymer aerogel -- 9.1 Conducting polymer aerogels- A property prospective -- 9.1.1 PEDOT aerogels. , 9.1.2 Polypyrrole (Ppy) aerogels -- 9.1.3 Polyaniline (PANi) aerogels -- 10. Sonogels -- 11. Graphene aerogel -- 11.1 Preparation of reduced graphene oxide aerogels -- 12. Carbon nanotubes (CNTs) aerogel -- 13. Hybrid aerogel -- 13.1 Class-I hybrid composites -- 13.2 Class-II hybrid composite -- 14. Application of porous aerogel -- 14.1 Thermal insulation -- 14.2 Removal of pollutants -- 14.3 Elimination of solid particle from gases -- 14.4 CO2 capture -- 14.5 Volatile organic compounds/catalysis -- 14.6 Water treatment -- 14.6.1 Oils in water -- 14.6.2 Wastewater and brackish water treatment -- 14.7 Biomedical applications -- 14.7.1 Aerogels for the administration of medicines -- 14.7.2 Tissue engineering -- 14.7.3 Biosensing -- References -- 3 -- Hybrid Silica Aerogel -- 1. Introduction -- 2. Hybrid silica aerogel -- 2.1 Polymer-silica aerogel -- 2.2 Biomolecules-silica aerogel -- 2.3 Graphene-silica aerogel -- 3. Final remarks -- Acknowledgements -- References -- 4 -- Silica Aerogel -- 1. Introduction -- 2. Synthesis methodology -- 2.1 Bare silica aerogels -- 2.2 Modified silica aerogels -- 3. Physico-chemical properties and applications -- 3.1 Thermal insulating application -- 3.2 Optical property application -- 3.3 Electronic application -- 3.4 Acoustic insulation applications -- 3.5 Biomedical applications -- 3.6 Environmental applications -- 3.7 Others applications -- 3.7.1 Space and detector -- 3.7.2 Oil spill clean-up -- 3.7.3 Aerospace -- Conclusions and future prospects -- References -- 5 -- Carbon Aerogels -- 1. Introduction -- 2. Types of carbon aerogels -- 2.1 Low flexible-carbon aerogel -- 2.2 Super flexible-carbon aerogel -- 2.3 Carbon nano tube aerogels -- 2.4 Graphene nano aerogel -- 2.5 Nano-diamond aerogel -- 2.6 Ni-doped carbon aerogel -- 2.7 Pt, Pd, Ag and Ru-doped carbon aerogel -- 2.8 Ce, Zr-based carbon aerogel. , 3. General characteristics and properties -- 3.1 Bulk density and porosity -- 3.2 Backbone density -- 3.3 Backbone connectivity -- 3.4 Pore connectivity -- 3.5 Pore size -- 3.6 Thermal properties -- 3.7 Electrical properties -- 3.8 Electrochemical properties -- 3.9 Mechanical properties -- 3.10 Gas-transport properties -- 3.11 Optical properties -- 4. Applications -- 4.1 Electrochemical field -- 4.2 Hydrogen storage -- 4.3 Catalyst support -- 4.4 Thermal insulation -- 4.5 Adsorbent for waste water treatment -- 4.6 Photocatalyst for waste water treatment -- 4.7 Sensor application -- Conclusions -- References -- 6 -- Magnetic Aerogels -- 1. Introduction -- 2. Cellulose magnetic aerogels -- 3. Magnetic graphene aerogel -- 4. Carbon magnetic aerogel -- 5. Magnetic silica aerogels -- 6. Magnetic pectin aerogel -- Conclusions -- Acknowledgements -- References -- 7 -- Properties of Aerogels -- 1. Introduction -- 2. Structure -- 3. Thermal properties -- 3.1 Silica aerogels -- 3.2 Organic and polymeric aerogels -- 3.3 Carbon aerogels -- 4. Electrical properties -- 4.1 Aerogels with low conductivity -- 4.2 Low dielectric constant materials -- 4.3 Aerogels with high conductivity -- 5. Optical properties -- 5.1 Radiators in Cherenkov counters -- 5.2 Fiber optics -- 5.3 Non reflective materials -- 6. Mechanical properties -- 7. Acoustic properties -- 8. Biocompatibility -- Conclusion -- Acknowledgements -- References -- 8 -- Tailor-Made Aerogels -- 1. Introduction -- 2. Existing and potential applications of aerogels -- 2.1 Pore engineering -- 2.2 Customizable surface and coating -- 2.3 Hybrid aerogels (HAgs): Influence of the sol-gel process on final properties -- 3. Applications of Tailor-made aerogels -- Conclusions -- Acknowledgments -- References -- 9 -- Aerogels Envisioning Future Applications -- 1. Introduction -- 2. Future applications of bioaerogels. , 2.1 Bioaerogels applied as functional foods -- 2.2 Bioaerogels applied as thickeners and stabilizers -- 2.3 Bioaerogels applied as medicines and scaffolding in tissue repair -- 3. Future applications of polymeric aerogel -- 3.1 Polymeric aerogel as impact absorbing materials -- 3.2 Polymeric aerogels used as catalyst supports -- 3.3 Polymeric aerogels can be used as aerospace components -- 4. Future applications of carbon aerogel -- 4.1 Future applications of carbon aerogels as photocatalytic components, electrodes and supercapacitor -- 4.2 Materials against electromagnetic interference, lipid adsorbents and scaffolds for polymers -- 5. Future applications of inorganic aerogels -- 5.1 Inorganic aerogels used as fuel cells -- 5.2 Inorganic aerogels used as catalysts -- Conclusion -- Acknowledgements -- The authors thank the Coordination for the Improvement of Higher Education Personnel (CAPES) and National Council of Scientific and Technological Development (CNPq) for funding this research. -- References -- 10 -- Recent Patents on Aerogels -- 1. Introduction -- 2. Applications -- 2.1 Patents on aerogel generators(WO 2004/022242 Al) -- 2.2 Aerogel blanket and its production (PCT/US2014/022919) -- 2.3 Cellulose aerogels PCT/GB2010/051542 -- 2.4 Some miscellaneous patents -- Acknowledgments -- References -- 11 -- State-of-the-Art and Prospective of Aerogels -- 1. Introduction -- 2.1 Synthesis of aerogels -- 3. State-of-the-art of aerogel -- 3.1 State-of-the-art properties of aerogel -- 3.2 State-of-the-art of preparation of aerogel -- 4. Future prospective of aerogel -- 4.1 Thermal insulation -- 4.2 Drug delivery -- 4.3 Energy storage device -- Acknowledgments -- References -- back-matter -- Keyword Index -- About the Editors.
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