Note: Cover -- Title Page -- Copyright Page -- Contents -- Preface -- Chapter 1 Application of MOFs and Their Derived Materials in Sensors -- 1.1 Introduction -- 1.2 Application of MOFs and Their Derived Materials in Sensors -- 1.2.1 Optical Sensor -- 1.2.1.1 Colorimetric Sensor -- 1.2.1.2 Fluorescence Sensor -- 1.2.1.3 Chemiluminescent Sensor -- 1.2.2 Electrochemical Sensor -- 1.2.2.1 Amperometric Sensor -- 1.2.2.2 Impedimetric, Electrochemiluminescence, and Photoelectrochemical Sensor -- 1.2.3 Field-Effect Transistor Sensor -- 1.2.4 Mass-Sensitive Sensor -- 1.3 Conclusion -- Acknowledgments -- References -- Chapter 2 Applications of Metal-Organic Frameworks (MOFs) and Their Derivatives in Piezo/Ferroelectrics -- 2.1 Introduction -- 2.1.1 Brief Introduction to Piezo/Ferroelectricity -- 2.2 Fundamentals of Piezo/Ferroelectricity -- 2.3 Metal-Organic Frameworks for Piezo/ Ferroelectricity -- 2.4 Ferro/Piezoelectric Behavior of Various MOFs -- 2.5 Conclusion -- References -- Chapter 3 Fabrication and Functionalization Strategies of MOFs and Their Derived Materials "MOF Architecture" -- 3.1 Introduction -- 3.2 Fabrication and Functionalization of MOFs -- 3.2.1 Metal Nodes -- 3.2.2 Organic Linkers -- 3.2.3 Secondary Building Units -- 3.2.4 Synthesis Methods -- 3.2.4.1 Hydrothermal and Solvothermal Method -- 3.2.4.2 Microwave Synthesis -- 3.2.4.3 Electrochemical Method -- 3.2.4.4 Mechanochemical Synthesis -- 3.2.4.5 Sonochemical (Ultrasonic Assisted) Method -- 3.2.4.6 Diffusion Method -- 3.2.4.7 Template Method -- 3.2.5 Synthesis Strategies -- 3.3 MOF Derived Materials -- 3.4 Conclusion -- References -- Chapter 4 Application of MOFs and Their Derived Materials in Molecular Transport -- 4.1 Introduction -- 4.2 MOFs as Nanocarriers for Membrane Transport -- 4.2.1 MIL-89 -- 4.2.2 MIL-88A -- 4.2.3 MIL-100 -- 4.2.4 MIL-101 -- 4.2.5 MIL-53 -- 4.2.6 ZIF-8. , 4.2.7 Zn-TATAT -- 4.2.8 BioMOF-1 (Zn) -- 4.2.9 UiO (Zr) -- 4.3 Conclusion -- References -- Chapter 5 Role of MOFs as Electro/-Organic Catalysts -- 5.1 What Is MOFs -- 5.2 MOFs as Electrocatalyst in Sensing Applications -- 5.3 MOFs as Organic Catalysts in Organic Transformations -- 5.4 Conclusion and Future Prospects -- References -- Chapter 6 Application of MOFs and Their Derived Materials in Batteries -- 6.1 Introduction -- 6.2 Metal-Organic Frameworks -- 6.2.1 Classification and Properties of Metal-Organic Frameworks -- 6.2.2 Potential Applications of MOFs -- 6.2.3 Synthesis of MOFs -- 6.3 Polymer Electrolytes -- 6.3.1 Historical Perspectives and Classification of Polymer Electrolytes -- 6.3.2 MOF Based Polymer Electrolytes -- 6.4 Ionic Liquids -- 6.4.1 Properties of Ionic Liquids -- 6.4.2 Ionic Liquid Incorporated MOF -- 6.5 Ion Transport in Polymer Electrolytes -- 6.5.1 General Description of Ionic Conductivity -- 6.5.2 Models for Ionic Transport in Polymer Electrolytes -- 6.5.3 Impedance Spectroscopy and Ionic Conductivity Measurements -- 6.5.4 Concept of Mismatch and Relaxation -- 6.5.5 Scaling of ac Conductivity -- 6.6 IL Incorporated MOF Based Composite Polymer Electrolytes -- 6.7 Conclusion and Perspectives -- References -- Chapter 7 Fine Chemical Synthesis Using Metal-Organic Frameworks as Catalysts -- 7.1 Introduction -- 7.2 Oxidation Reaction -- 7.2.1 Epoxidation -- 7.2.2 Sulfoxidation -- 7.2.3 Aerobic Oxidation of Alcohols -- 7.3 1,3-Dipolar Cycloaddition Reaction -- 7.4 Transesterification Reaction -- 7.5 C-C Bond Formation Reactions -- 7.5.1 Heck Reactions -- 7.5.2 Sonogashira Coupling -- 7.5.3 Suzuki Coupling -- 7.6 Conclusion -- References -- Chapter 8 Application of Metal Organic Framework and Derived Material in Hydrogenation Catalysis -- 8.1 Introduction -- 8.1.1 The Active Centers in Parent MOF Materials. , 8.1.2 The Active Centers in MOF Catalyst -- 8.1.3 Metal Nodes -- 8.2 Hydrogenation Reactions -- 8.2.1 Hydrogenation of Alpha-Beta Unsaturated Aldehyde -- 8.2.2 Hydrogenation of Cinnamaldehyde -- 8.2.3 Hydrogenation of Nitroarene -- 8.2.4 Hydrogenation of Nitro Compounds -- 8.2.5 Hydrogenation of Benzene -- 8.2.6 Hydrogenation of Quinoline -- 8.2.7 Hydrogenation of Carbon Dioxide -- 8.2.8 Hydrogenation of Aromatics -- 8.2.9 Hydrogenation of Levulinic Acid -- 8.2.10 Hydrogenation of Alkenes and Alkynes -- 8.2.11 Hydrogenation of Phenol -- 8.3 Conclusion -- References -- Chapter 9 Application of MOFs and Their Derived Materials in Solid-Phase Extraction -- 9.1 Solid-Phase Extraction -- 9.1.1 Materials in SPE -- 9.2 MOFs and COFs in Miniaturized Solid-Phase Extraction (µSPE) -- 9.3 MOFs and COFs in Miniaturized Dispersive Solid-Phase Extraction (D-µSPE) -- 9.4 MOFs and COFs in Magnetic-Assisted Miniaturized Dispersive Solid-Phase Extraction (m-D-µSPE) -- 9.5 Concluding Remarks -- Acknowledgments -- References -- Chapter 10 Anticancer and Antimicrobial MOFs and Their Derived Materials -- 10.1 Introduction -- 10.2 Anticancer MOFs -- 10.2.1 MOFs as Drug Carriers -- 10.2.2 MOFs in Phototherapy -- 10.3 Antibacterial MOFs -- 10.4 Antifungal MOFs -- References -- Chapter 11 Theoretical Investigation of Metal-Organic Frameworks and Their Derived Materials for the Adsorption of Pharmaceutical and Pe -- 11.1 Introduction -- 11.2 General Synthesis Routes -- 11.2.1 Hydrothermal Synthesis -- 11.2.2 Solvothermal Synthesis of MOFs -- 11.2.3 Room Temperature Synthesis -- 11.2.4 Microwave Assisted Synthesis -- 11.2.5 Mechanochemical Synthesis -- 11.2.6 Electrochemical Synthesis -- 11.3 Postsynthetic Modification in MOF -- 11.4 Computational Method -- 11.5 Results and Discussion. , 11.5.1 Binding Behavior Between MIL-100 With the Adsorbates (Diclofenac, Ibuprofen, Naproxen, and Oxybenzone) -- 11.6 Conclusion -- References -- Chapter 12 Metal-Organic Frameworks and Their Hybrid Composites for Adsorption of Volatile Organic Compounds -- 12.1 Introduction -- 12.2 VOCs and Their Potential Hazards -- 12.2.1 Other Sources of VOCs -- 12.3 VOCs Removal Techniques -- 12.4 Fabricated MOF for VOC Removal -- 12.4.1 MIL Series MOFs -- 12.4.2 Isoreticular MOFs -- 12.4.2.1 Adsorption Comparison of the Isoreticular MOFs -- 12.4.3 NENU Series MOFs -- 12.4.4 MOF-5, Eu-MOF, and MOF-199 -- 12.4.5 Amine-Impregnated MIL-100 -- 12.4.6 Biodegradable MOFs MIL-88 Series -- 12.4.7 Catalytic MOFs -- 12.4.8 Photo-Degradating MOFs -- 12.4.9 Some Other Studied MOFs -- 12.5 MOF Composites -- 12.5.1 MIL-101 Composite With Graphene Oxide -- 12.5.2 MIL-101 Composite With Graphite Oxide -- 12.6 Generalization Adsorptive Removal of VOCs by MOFs -- 12.7 Simple Modeling the Adsorption -- 12.7.1 Thermodynamic Parameters -- 12.7.2 Dynamic Sorption Methods -- 12.8 Factor Affecting VOCs Adsorption -- 12.8.1 Breathing Phenomena -- 12.8.2 Activation of MOFs -- 12.8.3 Applied Pressure -- 12.8.4 Relative Humidity -- 12.8.5 Breakthrough Conditions -- 12.8.6 Functional Group of MOFs -- 12.8.7 Concentration, Molecular Size, and Type of VOCs -- 12.9 Future Perspective -- References -- Chapter 13 Application of Metal-Organic Framework and Their Derived Materials in Electrocatalysis -- List of Abbreviations -- 13.1 Introduction -- 13.2 Perspective Synthesis of MOF and Their Derived Materials -- 13.3 MOF for Hydrogen Evolution Reaction -- 13.4 MOF for Oxygen Evolution Reaction -- 13.5 MOF for Oxygen Reduction Reaction -- 13.6 MOF for CO2 Electrochemical Reduction Reaction -- 13.6.1 Electrosynthesis of MOF for CO2 Reduction -- 13.6.2 Composite Electrodes as MOF for CO2 Reduction. , 13.6.3 Continuous Flow Reduction of CO2 -- 13.6.4 CO2 Electrochemical Reduction in Ionic Liquid -- 13.7 MOF for Electrocatalytic Sensing -- 13.8 Electrocatalytic Features of MOF -- 13.9 Conclusion -- Acknowledgment -- References -- Chapter 14 Applications of MOFs and Their Composite Materials in LightDriven Redox Reactions -- 14.1 Introduction -- 14.1.1 MOFs as Photocatalysts -- 14.1.2 Charge Transfer Mechanisms -- 14.1.3 Methods of Synthesis -- 14.2 Pristine MOFs and Their Application in Photocatalysis -- 14.2.1 Group 4 Metallic Clusters -- 14.2.2 Groups 8, 9, and 10 Metallic Clusters -- 14.2.3 Group 11 Metallic Clusters -- 14.2.4 Group 12 Metallic Clusters -- 14.3 Metal Nanoparticles-MOF Composites and Their Application in Photocatalysis -- 14.3.1 Ag-MOF Composites -- 14.3.2 Au-MOF Composites -- 14.3.3 Cu-MOF Composites -- 14.3.4 Pd-MOF Composites -- 14.3.5 Pt-MOF Composites -- 14.4 Semiconductor-MOF Composites and Their Application in Photocatalysis -- 14.4.1 TiO2-MOF Composites -- 14.4.2 Graphitic Carbon Nitride-MOF Composites -- 14.4.3 Bismuth-Based Semiconductors -- 14.4.4 Reduced Graphene Oxide-MOF Composites -- 14.4.5 Silver-Based Semiconductors -- 14.4.6 Other Semiconductors -- 14.5 MOF-Based Multicomponent Composites and Their Application in Photocatalysis -- 14.5.1 Semiconductor-Semiconductor-MOF Composites -- 14.5.2 Semiconductor-Metal-MOF Composites -- 14.6 Conclusions -- References -- Index -- Also of Interest -- Check out these other forthcoming and published titles from Scrivener Publishing -- EULA.

Note: Cover -- Title Page -- Copyright Page -- Contents -- Preface -- Chapter 1 Anti-Adhesive Coatings: A Technique for Prevention of Bacterial Surface Fouling -- 1.1 Bacterial Surface Fouling (Biofouling) -- 1.2 Negative Effects of Biofouling by Bacteria on Practical Applications -- 1.3 Anti-Adhesive Coatings for Preventing Bacterial Surface Fouling -- 1.3.1 Hydrophilic Polymers -- 1.3.2 Zwitterionic Polymers -- 1.3.3 Super-Hydrophobic Polymers -- 1.3.4 Slippery Liquid Infused Porous Surfaces (SLIPS) -- 1.3.5 Protein and Glycoprotein-Based Coatings -- 1.4 Bifunctional Coatings With Anti-Adhesive and Antibacterial Properties -- 1.5 Concluding Remarks -- Acknowledgments -- References -- Chapter 2 Lignin-Based Adhesives -- 2.1 Introduction -- 2.2 Native Lignin and Source of Technical Lignin -- 2.2.1 Native Lignin -- 2.2.2 Technical Lignins -- 2.3 Limitations of Technical Lignins -- 2.3.1 Heterogeneity of Technical Lignins -- 2.3.2 Reactivity of Technical Lignins -- 2.4 Lignin Pre-Treatment/Modification for Adhesive Application -- 2.4.1 Physical Pre-Treatment -- 2.4.2 Chemical Modification -- 2.5 Challenges and Prospects -- 2.6 Conclusions -- References -- Chapter 3 Green Adhesive for Industrial Applications -- 3.1 Introduction -- 3.2 Advanced Green Adhesives Categories- Industrial Applications -- 3.2.1 Keta Spire Poly Etherether Ketone Powder Coating -- 3.2.2 Bio-Inspired Adhesive in Robotics Field Application -- 3.2.3 Bio-Inspired Synthetic Adhesive in Space Application -- 3.2.3.1 Micro Structured Dry Adhesive Fabrication for Space Application -- 3.2.4 Natural Polymer Adhesive for Wood Panel Industry -- 3.2.5 Tannin Based Bio-Adhesive for Leather Tanning Industry -- 3.2.6 Conductive Adhesives in Microelectronics Industry -- 3.2.7 Bio-Resin Adhesive in Dental Industry -- 3.2.8 Green Adhesive in Fiberboard Industry -- 3.3 Conclusions and Future Scope. , References -- Chapter 4 Green Adhesives for Biomedical Applications -- 4.1 Introduction -- 4.2 Main Raw Materials of Green Adhesives: Structure, Composition, and Properties -- 4.2.1 Chitosan -- 4.2.2 Alginate -- 4.2.3 Lignin -- 4.2.4 Lactic Acid PLA -- 4.3 Properties Characterization of Green Adhesives for Biomedical Applications -- 4.3.1 Diffraction X-Rays (DRX) -- 4.3.2 Atomic Force Microscopy (AFM) -- 4.3.3 Scanning Electron Microscope (SEM Images) -- 4.3.4 Wettability or Contact Angle (CA) -- 4.3.5 Fourier Transform Infrared Spectroscopy (FTIR) -- 4.3.6 Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) -- 4.3.7 Thermal Analysis (TG/DTG/DTA and DSC Curves) -- 4.3.8 Surface Area and Porosimetry Analyzer (ASAP) -- 4.3.9 Mechanical Properties of Green Adhesives -- 4.4 Biomedical Applications of Natural Polymers -- 4.4.1 Alginate -- 4.4.1.1 Biomedical Applications of Alginate -- 4.4.2 Chitosan -- 4.4.2.1 Biomedical Applications of Chitosan -- 4.4.3 Lignin -- 4.4.3.1 Biomedical Applications of Lignin -- 4.4.4 Polylactide (PLA) -- 4.4.4.1 Biomedical Applications of PLA -- 4.5 Final Considerations -- Acknowledgements -- References -- Chapter 5 Waterborne Adhesives -- 5.1 Introduction -- 5.1.1 Motivation for the Use of Waterborne Adhesives -- 5.1.1.1 Sustainability and Environment Regulations -- 5.1.1.2 Circular Economy -- 5.1.1.3 Avoid Harmful Emissions -- 5.1.1.4 Development of Novel and Sustainable End Products -- 5.1.2 Environmental Effects and Mankind Toxicity Analysis -- 5.2 Performance of Waterborne Adhesives: An Overview -- 5.2.1 Waterborne Polyurethane (WBPU) Adhesives -- 5.2.1.1 Chemical Structure of Waterborne PU -- 5.2.1.2 Performances of WBPU Adhesives -- 5.2.2 Waterborne Epoxy Adhesive -- 5.3 Conclusions -- References -- Chapter 6 Using Polyfurfuryl Alcohol as Thermoset Adhesive/Sealant -- 6.1 Introduction. , 6.2 Furfuryl Alcohol as Adhesives -- 6.3 Polyfurfuryl Alcohol as Sealants -- 6.3.1 Effect of Different Parameters on the Curing of PFA-Based Sealants -- 6.4 Applications -- 6.5 Conclusions -- Acknowledgement -- References -- Chapter 7 Bioadhesives -- 7.1 Introduction -- 7.2 History of Bioadhesives -- 7.3 Classification of Bioadhesives -- 7.4 Mechanism of Bioadhesion -- 7.4.1 Mechanical Interlocking -- 7.4.2 Chain Entanglement -- 7.4.3 Intermolecular Bonding -- 7.4.4 Electrostatic Bonding -- 7.5 Testing of Bioadhesives -- 7.5.1 In Vitro Methods -- 7.5.1.1 Shear Stress Measurements -- 7.5.1.2 Peel Strength Evaluation -- 7.5.1.3 Flow Through Experiment and Plate Method -- 7.5.2 Ex Vitro Methods -- 7.5.2.1 Adhesion Weight Method -- 7.5.2.2 Fluorescent Probe Methods -- 7.5.2.3 Falling Liquid Film Method -- 7.6 Application of Bioadhesives -- 7.6.1 Bioadhesives as Drug Delivery Systems -- 7.6.2 Bioadhesives as Fibrin Sealants -- 7.6.3 Bioadhesives as Protein-Based Adhesives -- 7.6.4 Bioadhesives in Tissue Engineering -- 7.7 Conclusion -- References -- Chapter 8 Polysaccharide-Based Adhesives -- 8.1 Introduction -- 8.2 Cellulose-Derived Adhesive -- 8.2.1 Esterification -- 8.2.1.1 Cellulose Nitrate -- 8.2.1.2 Cellulose Acetate -- 8.2.1.3 Cellulose Acetate Butyrate -- 8.2.2 Etherification -- 8.2.2.1 Methyl Cellulose -- 8.2.2.2 Ethyl Cellulose -- 8.2.2.3 Carboxymethyl Cellulose -- 8.3 Starch-Derived Adhesives -- 8.3.1 Alkali Treatment -- 8.3.2 Acid Treatment -- 8.3.3 Heating -- 8.3.4 Oxidation -- 8.4 Natural Gums Derived-Adhesives -- 8.5 Fermentation-Based Adhesives -- 8.6 Enzyme Cross-Linked-Based Adhesives -- 8.7 Micro-Biopolysaccharide-Based Adhesives -- 8.8 Mechanism of Adhesion -- 8.9 Tests for Adhesion Strength -- 8.10 Applications -- 8.10.1 Biomedical Applications -- 8.10.2 Food Stuffs Applications -- 8.10.3 Pharmaceutical Applications. , 8.10.4 Agricultural Applications -- 8.10.5 Cigarette Manufacturing -- 8.10.6 Skin Cleansing Applications -- 8.11 Conclusion -- References -- Chapter 9 Wound Healing Adhesives -- 9.1 Introduction -- 9.2 Wound -- 9.2.1 Types of Wounds -- 9.2.1.1 Acute Wounds -- 9.2.1.2 Chronic Wounds -- 9.3 Structure and Function of the Skin -- 9.4 Mechanism of Wound Healing -- 9.5 Wound Closing Techniques -- 9.6 Wound Healing Adhesives -- 9.7 Types of Wound Healing Adhesives Based Upon Site of Application -- 9.7.1 External Use Wound Adhesives -- 9.7.1.1 Steps for Applying External Wound Healing Adhesives on Skin [30] -- 9.7.2 Internal Use Wound Adhesives -- 9.8 Types of Wound Healing Adhesives Based Upon Chemistry -- 9.8.1 Natural Wound Healing Adhesives -- 9.8.1.1 Fibrin Sealants/Fibrin-Based Tissue Adhesives -- 9.8.1.2 Albumin-Based Adhesives -- 9.8.1.3 Collagen and Gelatin-Based Wound Healing Adhesives -- 9.8.1.4 Starch -- 9.8.1.5 Chitosan -- 9.8.1.6 Dextran -- 9.8.2 Synthetic Wound Healing Adhesives -- 9.8.2.1 Cyanoacrylate -- 9.8.2.2 Poly Ethylene Glycol-Based Wound Adhesives (PEG) -- 9.8.2.3 Hydrogels -- 9.8.2.4 Polyurethane -- 9.9 Summary -- References -- Chapter 10 Green-Wood Flooring Adhesives -- 10.1 Introduction -- 10.2 Wood Flooring -- 10.2.1 Softwood Flooring -- 10.2.2 Hardwood Flooring -- 10.2.3 Engineered Wood Flooring -- 10.2.4 Laminate Flooring -- 10.2.5 Vinyl Flooring -- 10.2.6 Agricultural Residue Wood Flooring Panels -- 10.3 Recent Advances About Green Wood-Flooring Adhesives -- 10.3.1 Xylan -- 10.3.2 Modified Cassava Starch Bioadhesives -- 10.3.3 High-Efficiency Bioadhesive -- 10.3.4 Bioadhesive Made From Soy Protein and Polysaccharide -- 10.3.5 Green Cross-Linked Soy Protein Wood Flooring Adhesive -- 10.3.6 "Green" Bio-Thermoset Resins Derived From Soy Protein Isolate and Condensed Tannins. , 10.3.7 Development of Green Adhesives Using Tannins and Lignin for Fiberboard Manufacturing -- 10.3.8 Cottonseed Protein as Wood Adhesives -- 10.3.9 Chitosan as an Adhesive -- 10.3.10 PE-cg-MAH Green Wood Flooring Adhesive -- References -- Chapter 11 Synthetic Binders for Polymer Division -- List of Abbreviations -- 11.1 Introduction -- 11.2 Classification of Adhesives Based on Its Chemical Properties -- 11.2.1 Thermoset Adhesives -- 11.2.2 Thermoplastic Adhesives -- 11.2.3 Adhesive Blends -- 11.3 Adhesives Characteristics -- 11.4 Adhesives Classification Based on Its Function -- 11.4.1 Permanent Adhesives -- 11.4.2 Removable Adhesives -- 11.4.3 Repositionable Adhesives -- 11.4.4 Blended Adhesives -- 11.4.5 Anaerobic Adhesives -- 11.4.6 Aromatic Polymer Adhesives -- 11.4.7 Asphalt -- 11.4.8 Adhesives Based on Butyl Rubber -- 11.4.9 Cellulose Ester Adhesives -- 11.4.10 Adhesives Based on Cellulose Ether -- 11.4.11 Conductive Adhesives -- 11.4.12 Electrically Conductive Adhesive Materials -- 11.4.13 Thermally Conductive Adhesives -- 11.5 Resin -- 11.5.1 Unsaturated Polyester Resin -- 11.5.2 Monomers -- 11.5.2.1 Unsaturated Polyester -- 11.5.2.2 Alcohol Constituents -- 11.5.2.3 Constituents Like Anhydride and Acid -- 11.5.3 Vinyl Monomers of Unsaturated Polyester Resins -- 11.5.4 Styrenes -- 11.5.5 Acrylates and Methacrylates -- 11.5.6 Vinyl Ethers -- 11.5.7 Fillers -- 11.6 Polyurethanes -- 11.6.1 Monomers -- 11.6.1.1 Diisocyanates -- 11.6.1.2 Phosgene Route -- 11.6.1.3 Phosgene-Free Route -- 11.6.1.4 Polyols -- 11.6.1.5 Vinyl Functionalized Polyols -- 11.6.1.6 Polyols Based on Modified Polyurea -- 11.6.1.7 Polyols Based on Polyester -- 11.6.1.8 Acid and Alcohols-Based Polyesters -- 11.6.2 Rectorite Nanocomposites -- 11.6.3 Zeolite -- 11.7 Epoxy Resins -- 11.7.1 Monomers -- 11.7.1.1 Epoxides -- 11.7.1.2 Hyper Branched Polymers. , 11.7.2 Epoxide Resins Based on Liquid Crystalline Structure.