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電子ブック

EB
Sensuke Ogoshi
出版情報: Wiley Online Library - AutoHoldings Books , John Wiley & Sons, Inc., 2020
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Preface
Reactions via Nickelacycles / Part I:
Formation of Nickelacycles and Reaction with Carbon Monoxide / Sensuke Ogoshi1:
Introduction / 1.1:
Formation of Hetero-nickelacycles from Nickel(O) / 1.2:
Stoichiometric Reaction of Hetero-nickelacycles with Carbon Monoxide / 1.3:
References
Transformation of Aldehydes via Nickelacycles / Yoichi Hashimoto2:
Introduction and Scope of This Chapter / 2.1:
Catalytic Transformation of Aldehydes Through Three-Membered Oxanickelacycle Complexes / 2.2:
Catalytic Transformation of Aldehydes Through Five-Membered Oxanickelacycle Complexes / 2.3:
Catalytic Transformation of Aldehydes Through Seven-Membered Oxanickelacycle Complexes / 2.4:
Conclusion and Outlook / 2.5:
Transformation of Imines via Nickelacycles / Masato Ohashi3:
[2 + 2 + 1] Carbonylative Cycloaddition of an Imine and Either an Alkyne or an Alkene Leading to ¿-Lactams / 3.1:
[2 + 2 + 2] Cycloaddition Reaction of an Imine with Two Alkynes: Formation of 1,2-Dihydropyridine Derivatives / 3.3:
Three-Component Coupling and Cyclocondensation Reactions of an Imine, an Alkyne, and Alkylmetal Reagents / 3.4:
Asymmetric C-C Bond Formation Reactions via Nickelacycles / Ravindra Kumar and Sensuke Ogoshi4:
Enantioselective Reactions Involving Nickelacycles / 4.1:
Nickel-Catalyzed Asymmetric Coupling of Alkynes and Aldehydes / 4.2.1:
Nickel-Catalyzed Asymmetric Reductive Coupling of Alkynes and Aldehydes / 4.2.1.1:
Nickel-Catalyzed Asymmetric Alkylative Coupling of Alkynes and Aldehydes / 4.2.1.2:
Nickel-Catalyzed Asymmetric Coupling of Alkynes and Imines / 4.2.2:
Nickel-Catalyzed Asymmetric Coupling of 1,3-Enynes and Aldehydes / 4.2.3:
Nickel-Catalyzed Asymmetric Coupling of 1,3-Enynes and Ketones / 4.2.4:
Nickel-Catalyzed Asymmetric Coupling of 1,3-Dienes and Aldehydes / 4.2.5:
Nickel-Catalyzed Asymmetric Coupling of Enones and Alkynes / 4.2.6:
Nickel-Catalyzed Asymmetric Alkylative Coupling of Enones and Alkynes / 4.2.6.1:
Nickel-Catalyzed Asymmetric Coupling of Arylenoates and Alkynes / 4.2.6.2:
Nickel-Catalyzed Asymmetric Coupling of Diynes with Ketenes / 4.2.8:
Nickel-Catalyzed Asymmetric Coupling of Allenes, Aldehydes, and Silanes / 4.2.9:
Nickel-Catalyzed Asymmetric Coupling of Allenes and Isocyanates / 4.2.10:
Nickel-Catalyzed Asymmetric Coupling of Alkenes, Aldehydes, and Silanes / 4.2.11:
Nickel-Catalyzed Asymmetric Coupling of Formamide and Alkene / 4.2.12:
Nickel-Catalyzed Asymmetric Coupling of Alkynes and Cyclopropyl Carboxamide / 4.2.13:
Miscellaneous / 4.3:
Nickel-Catalyzed Asymmetric Annulation of Pyridones via Hydroarylation to Alkenes / 4.3.1:
Nickel-Catalyzed Asymmetric Synthesis of Benzoxasilole / 4.3.2:
Overview and Future Perspective / 4.4:
Functionalization of Unreactive Bonds / Part II:
Recent Advances in Ni-Catalyzed Chelation-Assisted Direct Functionalization of Inert C-H Bonds / Yon-Hua Liu and Fang Hu and Bing-Feng Shi5:
Ni-Catalyzed Functionalization of Inert C-H Bonds Assisted by Bidentate Directing Groups / 5.1:
Arylation / 5.2.1:
Alkylation / 5.2.2:
Alkenylation / 5.2.3:
Alkynylation / 5.2.4:
Other C-C Bond Formation Reactions Directed by Bidentate Directing Group / 5.2.5:
C-N Bond Formation / 5.2.6:
C-Chalcogen (Chalcogen = O, S, Se) Bond Formation / 5.2.7:
C-Halogen Bond Formation / 5.2.8:
Ni-Catalyzed Functionalization of Inert C-H Bonds Assisted by Monodentate Directing Groups / 5.3:
C-Calcogen Bond Formation / 5.3.1:
Summary / 5.4:
C-C Bond Functionalization / Yoshiaki Nakao6:
C-C Bond Functionalization of Three-Membered Rings / 6.1:
C-C Bond Functionalization of Four- and Five-Membered Rings / 6.3:
C-C Bond Functionalization of Less Strained Molecules / 6.4:
C-CN Bond Functionalization / 6.5:
Summary and Outlook / 6.6:
C-O Bond Transformations / Mamoru Tobisu7:
C(aryl)-O Bond Cleavage / 7.1:
Aryl Esters, Carbamates, and Carbonates / 7.2.1:
Aryl Ethers / 7.2.2:
Arenols / 7.2.3:
C(benzyl)-O Bond Cleavage / 7.3:
Benzyl Esters and Carbamates / 7.3.1:
Benzyl Ethers / 7.3.2:
C(acyl)-O Bond Cleavage / 7.4:
Coupling Reactions via Ni(I) and/or Ni(III) / 7.5:
Photo-Assisted Nickel-Catalyzed Cross-Coupling Processes / Christophe Lévéque and Cyril Ollivier and Louis Fensterbank8:
Development of Visible-Light Photoredox/Nickel Dual Catalysis / 8.1:
For the Formation of Carbon-Carbon Bonds / 8.2.1:
Starting from Organotrifluoroborates / 8.2.1.1:
Starting from Carboxylates or Keto Acids or from Methylanilines / 8.2.1.2:
Starting from Alkylsilicates / 8.2.1.3:
Starting from 1,4-Dihydropyridines / 8.2.1.4:
Starting from Alkylsulfinates / 8.2.1.5:
Starting from Alkyl Bromides / 8.2.1.6:
Starting from Xanthates / 8.2.1.7:
Starting from Sp3 CH Bonds / 8.2.1.8:
For the Formation of Carbon-Heteroatom Bonds / 8.2.2:
Formation of C-O Bond / 8.2.2.1:
Formation of C-P Bond / 8.2.2.2:
Formation of C-S Bond / 8.2.2.3:
Energy-Transfer-Mediated Nickel Catalysis / 8.3:
Conclusion / 8.4:
Cross-Electrophile Coupling: Principles and New Reactions / Matthew M. Goldfogel and Liangbin Huang and Daniel J. Weix9:
Mechanistic Discussion of Cross-Electrophile Coupling / 9.1:
C(sp2)-C(sp3) Bond Formation / 9.3:
Cross-Electrophile Coupling of Aryl-X and Alkyl-X / 9.3.1:
Cross-Electrophile Coupling of ArX and Bn-X / 9.3.2:
Cross-Electrophile Coupling of ArX and Allyl-X / 9.3.3:
Vinyl-X with R-X / 9.3.4:
Acyl-X with Alkyl-X / 9.3.5:
C(sp2)-C(sp2) Coupling / 9.4:
Aryl-X/Vinyl-X + Aryl-X/Vinyl-X / 9.4.1:
Aryl-X + Acyl-X / 9.4.2:
C(sp3)-C(sp3) Coupling / 9.5:
C(sp)-C(sp3) Coupling / 9.6:
Multicomponent Reactions / 9.7:
Future of the Field / 9.8:
Organometallic Chemistry of High-Valent Ni(III) and Ni(IV) Complexes / Liviu M. Mirica and Sofia M. Smith and Leonel Griego10:
Organometallic Ni(III) Complexes / 10.1:
Organometallic Ni(IV) Complexes / 10.3:
Other High-Valent Ni Complexes / 10.4:
Additional NiIII Complexes / 10.4.1:
Additional NiIV Complexes / 10.4.2:
Conclusions and Outlook / 10.5:
Carbon Dioxide Fixation / Part IV:
Carbon Dioxide Fixation via Nickelacycle / Ryohei Doi and Yoshihiro Sato11:
Introduction: Carbon Dioxide as a C1 Building Block / 11.1:
Formation, Structure, and Reactivity of Nickelalactone / 11.2:
Formation and Characterization of Nickelalactone via Oxidative Cyclization with CO2 / 11.2.1:
Reaction with Alkene / 11.2.1.1:
Reaction with Allene / 11.2.1.2:
Reaction with Diene / 11.2.1.3:
Reaction with Alkyne / 11.2.1.4:
Other Related Reactions / 11.2.1.5:
Generation of Nickelalactone Without CO2 / 11.2.1.6:
Reactivity of Nickelalactone / 11.2.2:
Transmetalation with Organometallic Reagent / 11.2.2.1:
ß-Hydride Elimination / 11.2.2.2:
Insertion of Another Unsaturated Molecule / 11.2.2.3:
Retro-cyclization / 11.2.2.4:
Nucleophilic Attack / 11.2.2.5:
Oxidation / 11.2.2.6:
Ligand Exchange / 11.2.2.7:
Catalytic Transformation via Nickelalactone 1: Reactions of Alkynes / 11.3:
Synthesis of Pyrone / 11.3.1:
Initial Finding / 11.3.1.1:
Reaction of Diynes with CO2 / 11.3.1.2:
Synthesis of ¿,ß-Unsaturated Ester / 11.3.2:
Electrochemical Reactions / 11.3.2.1:
Reduction with Organometallic Reagents / 11.3.2.2:
Catalytic Transformation via Nickelalactone 2: Reactions of Alkenes and Related Molecules / 11.4:
Transformation of Diene, Allene, and Substituted Alkene / 11.4.1:
Coupling of Diene with CO2 / 11.4.1.1:
Electrochemical Process / 11.4.1.2:
Use of Reductant / 11.4.1.3:
Synthesis of Acrylic Acid from Ethylene and CO2 / 11.4.2:
Before the Dawn / 11.4.2.1:
Development of Catalytic Reaction / 11.4.2.2:
Concluding Remarks / 11.5:
Relevance of Ni(I) in Catalytic Carboxylation Reactions / Rosie J. Somerville and Ruben Martin12:
Mechanistic Building Blocks / 12.1:
Additives / 12.2.1:
Coordination of CO2 / 12.2.2:
Insertion/C-C Bond Formation / 12.2.3:
Ligand Effects / 12.2.4:
Oxidative Addition / 12.2.5:
Oxidation State / 12.2.6:
Single Electron Transfer (SET) / 12.2.7:
Electrocarboxylation / 12.2.8:
Phosphine Ligands / 12.3.1:
Bipyridine and Related ¿-Diimine Ligands / 12.3.3:
Salen Ligands / 12.3.4:
Non-electrochemical Methods / 12.3.5:
Aryl Halides / 12.4.1:
Benzyl Electrophiles / 12.4.2:
Carboxylation of Unactivated Alkyl Electrophiles / 12.4.3:
Carboxylation of Allyl Electrophiles / 12.4.4:
Unsaturated Systems / 12.4.5:
Conclusions / 12.5:
Index
Preface
Reactions via Nickelacycles / Part I:
Formation of Nickelacycles and Reaction with Carbon Monoxide / Sensuke Ogoshi1:
2.

電子ブック

EB
Crocker, Santillan-Jimenez Eduardo
出版情報: Wiley Online Library - AutoHoldings Books , John Wiley & Sons, Inc., 2020
所蔵情報: loading…
目次情報: 続きを見る
Preface
Upgrading of Biomass via Catalytic Fast Pyrolysis (CFP) / Charles A. Mullen1:
Introduction / 1.1:
Catalytic Pyrolysis Over Zeolites / 1.1.1:
Catalytic Pyrolysis Over HZSM-5 / 1.1.1.1:
Deactivation of HZSM-5 During CFP / 1.1.1.2:
Modification of ZSM-5 with Metals / 1.1.1.3:
Modifications of ZSM-5 Pore Structure / 1.1.1.4:
CFP with Metal Oxide Catalysts / 1.1.2:
CFP to Produce Fine Chemicals / 1.1.3:
Outlook and Conclusions / 1.1.4:
References
The Upgrading of Bio-Oil via Hydrodeoxygenation / Adetoyese O. Oyedun and Madhumita Patel and Mayank Kumar and Amit Kumar2:
Hydrodeoxygenation (HDO) / 2.1:
Hydrodeoxygenation of Phenol as a Model Compound / 2.2.1:
HDO of Phenolic (Guaiacol) Model Compounds / 2.2.1.1:
HDO of Phenolic (Anisole) Model Compounds / 2.2.1.2:
HDO of Phenolic (Cresol) Model Compounds / 2.2.1.3:
Hydrodeoxygenation of Aldehyde Model Compounds / 2.2.2:
Hydrodeoxygenation of Carboxylic Acid Model Compounds / 2.2.3:
Hydrodeoxygenation of Alcohol Model Compounds / 2.2.4:
Hydrodeoxygenation of Carbohydrate Model Compounds / 2.2.5:
Chemical Catalysts for the HDO Reaction / 2.3:
Catalyst Promoters for HDO / 2.3.1:
Catalyst Supports for HDO / 2.3.2:
Catalyst Selectivity for HDO / 2.3.3:
Catalyst Deactivation During HDO / 2.3.4:
Research Gaps / 2.4:
Conclusions / 2.5:
Acknowledgments
Upgrading of Bio-oil via Fluid Catalytic Cracking / Idoia Hita and Jose Maria Arandes and Javier Bilbao3:
Bio-oil / 3.1:
Bio-oil Production via Fast Pyrolysis / 3.2.1:
General Characteristics, Composition, and Stabilization of Bio-oil / 3.2.2:
Adjustment of Bio-oil Composition Through Pyrolytic Strategies / 3.2.2.1:
Bio-oil Stabilization / 3.2.2.2:
Valorization Routes for Bio-oil / 3.2.3:
Hydroprocessing / 3.2.3.1:
Steam Reforming / 3.2.3.2:
Extraction of Valuable Components from Bio-oil / 3.2.3.3:
Catalytic Cracking of Bio-oil: Fundamental Aspects / 3.3:
The FCC Unit / 3.3.1:
Cracking Reactions and Mechanisms / 3.3.2:
Cracking of Oxygenated Compounds / 3.3.3:
Cracking of Bio-oil / 3.3.4:
Bio-oil Cracking in the FCC Unit / 3.4:
Cracking of Model Oxygenates / 3.4.1:
Coprocessing of Oxygenates and Their Mixtures with Vacuum Gas Oil (VGO) / 3.4.2:
Cracking of Bio-oil and Its Mixtures with VGO / 3.4.3:
Conclusions and Critical Discussion / 3.5:
Stabilization of Bio-oil via Esterification / Xun Hu4:
Reactions of the Main Components of Bio-Oil Under Esterification Conditions / 4.1:
Sugars / 4.2.1:
Carboxylic Acids / 4.2.2:
Furans / 4.2.3:
Aldehydes and Ketones / 4.2.4:
Phenolics / 4.2.5:
Other Components / 4.2.6:
Processes for Esterification of Bio-oil / 4.3:
Esterification of Bio-oil Under Subcritical or Supercritical Conditions / 4.3.1:
Removal of the Water in Bio-oil to Enhance Conversion of Carboxylic Acids / 4.3.2:
In-line Esterification of Bio-oil / 4.3.3:
Esterification Coupled with Oxidation / 4.3.4:
Esterification Coupled with Hydrogenation / 4.3.5:
Steric Hindrance in Bio-oil Esterification / 4.3.6:
Coking in Esterification of Bio-oil / 4.3.7:
Effects of Bio-oil Esterification on the Subsequent Hydrotreatment / 4.3.8:
Catalysts / 4.4:
Summary and Outlook / 4.5:
Catalytic Upgrading of Holocellulose-Derived C5 and C6 Sugars / Xingguang Zhang and Zhijun Tai and Amin Osatiashtiani and Lee Durndell and Adam F. Lee and Karen Wilson5:
Catalytic Transformation of C5-C6 Sugars / 5.1:
Isomerization Catalysts / 5.2.1:
Zeolites / 5.2.1.1:
Hydrotalcites / 5.2.1.2:
Other Solid Catalysts / 5.2.1.3:
Dehydration Catalysts / 5.2.2:
Zeolitic and Mesoporous Brønsted Solid Acids / 5.2.2.1:
Sulfonic Acid Functionalized Hybrid Organic-Inorganic Silicas / 5.2.2.2:
Metal-Organic Frameworks / 5.2.2.3:
Supported Ionic Liquids / 5.2.2.4:
Catalysts for Tandem Isomerization and Dehydration of C5-C6 Sugars / 5.2.3:
Bifunctional Zeolites and Mesoporous Solid Acids / 5.2.3.1:
Metal Oxides, Sulfates, and Phosphates / 5.2.3.2:
Catalysts for the Hydrogenation of C5-C6 Sugars / 5.2.3.3:
Ni Catalysts / 5.2.4.1:
Ru Catalysts / 5.2.4.2:
Pt Catalysts / 5.2.4.3:
Other Hydrogenation Catalysts / 5.2.4.4:
Hydrogenolysis Catalysts / 5.2.5:
Other Reactions / 5.2.6:
Conclusions and Future Perspectives / 5.3:
Chemistry of C-C Bond Formation Reactions Used in Biomass Upgrading: Reaction Mechanisms, Site Requirements, and Catalytic Materials / Tuong V. Bui and Nhung Duong and Felipe Anaya and Duong Ngo and Gap Warakunwit and Daniel E. Resasco6:
Mechanisms and Site Requirements of C-C Coupling Reactions / 6.1:
Aldol Condensation: Mechanism and Site Requirement / 6.2.1:
Base-Catalyzed Aldol Condensation / 6.2.1.1:
Acid-Catalyzed Aldol Condensation: Mechanism and Site Requirement / 6.2.1.2:
Alkylation: Mechanism and Site Requirement / 6.2.2:
Lewis Acid-Catalyzed Alkylation Mechanism / 6.2.2.1:
Brønsted Acid-Catalyzed Alkylation Mechanism / 6.2.2.2:
Base-Catalyzed Alkylation: Mechanism and Site Requirement / 6.2.2.3:
Hydroxyalkylation: Mechanism and Site Requirement / 6.2.3:
Brønsted Acid-Catalyzed Mechanism / 6.2.3.1:
Site Requirement / 6.2.3.2:
Acylation: Mechanism and Site Requirement / 6.2.4:
Mechanistic Aspects of Acylation Reactions / 6.2.4.1:
Role of Brønsted vs. Lewis Acid in Acylation Over Zeolites / 6.2.4.2:
Ketonization: Mechanism and Site Requirement / 6.2.5:
Mechanism of Surface Ketonization / 6.2.5.1:
Optimization and Design of Catalytic Materials for C-C Bond Forming Reactions / 6.2.5.2:
Oxides / 6.3.1:
Magnesia (MgO) / 6.3.1.1:
Zirconia (ZrO2) / 6.3.1.2:
ZSM-5 / 6.3.2:
HY / 6.3.2.2:
HBEA / 6.3.2.3:
Downstream Conversion of Biomass-Derived Oxygenates to Fine Chemicals / Michèle Besson and Stéphane Loridant and Noémie Perret and Catherine Pinel7:
Selective Catalytic Oxidation / 7.1:
Catalytic Oxidation of Glycerol / 7.2.1:
Glycerol to Glyceric Acid (GLYAC) / 7.2.2.1:
Glycerol to Tartronic Acid (TARAC) / 7.2.2.2:
Glycerol to Dihydroxyacetone (DHA) / 7.2.2.3:
Glycerol to Mesoxalic Acid (MESAC) / 7.2.2.4:
Glycerol to Glycolic Acid (GLYCAC) / 7.2.2.5:
Glycerol to Lactic Acid (LAC) / 7.2.2.6:
Oxidation of 5-HydroxymethylfurfuraI (HMF) / 7.2.3:
HMF to 2,5-Furandicarboxylic Acid (FDCA) / 7.2.3.1:
HMF to 2,5-Diformylfuran (DFF) / 7.2.3.2:
HMF to 5-Hydroxymethyl-2-furancarboxylic Acid (HMFCA) or 5-Formyl-2-furancarboxylic Acid (FFCA) / 7.2.3.3:
Hydrogenation/Hydrogenolysis / 7.3:
Hydrogenolysis of Polyols / 7.3.1:
Hydrodeoxygenation of Polyols / 7.3.2.1:
C-C Hydrogenolysis of Polyols / 7.3.2.2:
Hydrogenation of Carboxylic Acids / 7.3.3:
Levulinic Acid / 7.3.3.1:
Succinic Acid / 7.3.3.2:
Selective Hydrogenation of Furanic Compounds / 7.3.4:
Reductive Amination of Acids and Furans / 7.3.5:
Catalyst Design for the Dehydration of Biosourced Molecules / 7.4:
Glycerol to Acrolein / 7.4.1:
Lactic Acid to Acrylic Acid / 7.4.3:
Sorbitol to Isosorbide / 7.4.4:
Conclusions and Outlook / 7.5:
Conversion of Lignin to Value-added Chemicals via Oxidative Depolymerization / Justin K. Mobley8:
Cautionary Statements / 8.1:
Catalytic Systems for the Oxidative Depolymerization of Lignin / 8.2:
Enzymes and Bio-mimetic Catalysts / 8.2.1:
Cobalt Schiff Base Catalysts / 8.2.2:
Vanadium Catalysts / 8.2.3:
Methyltrioxorhenium (MTO) Catalysts / 8.2.4:
Commercial Products from Lignin / 8.3:
Stepwise Depolymerization of ß-O-4 Linkages / 8.4:
Benzylic Oxidation / 8.4.1:
Secondary Depolymerization / 8.4.2:
Heterogeneous Catalysts for Lignin Depolymerization / 8.5:
Outlook / 8.6:
Lignin Valorization via Reductive Depolymerization / Yang (Vanessa) Song9:
Late-stage Reductive Lignin Depolymerization / 9.1:
Mild Hydroprocessing / 9.2.1:
Harsh Hydroprocessing / 9.2.2:
Bifunctional Hydroprocessing / 9.2.3:
Liquid Phase Reforming / 9.2.4:
Reductive Lignin Depolymerization Using Hydrosilanes, Zinc, and Sodium / 9.2.5:
Reductive Catalytic Fractionation (RCF) / 9.3:
Reaction Conditions / 9.3.1:
Lignocellulose Source / 9.3.2:
Applied Catalyst / 9.3.3:
Acknowledgment / 9.4:
Conversion of Lipids to Biodiesel via Esterification and Transesterification / Amin Talebian-Kiakalaieh and Amin Nor Aishah Saidina10:
Different Feedstocks tor Biodiesel Production / 10.1:
Biodiesel Production / 10.3:
Algal Bio diesel Production / 10.3.1:
Nutrients for Microalgae Growth / 10.3.1.1:
Microalgae Cultivation System / 10.3.1.2:
Harvesting / 10.3.1.3:
Drying / 10.3.1.4:
Lipid Extraction / 10.3.1.5:
Catalytic Transesterification / 10.4:
Homogeneous Catalysts / 10.4.1:
Alkali Catalysts / 10.4.1.1:
Acid Catalysts / 10.4.1.2:
Two-step Esterification-Transesterification Reactions / 10.4.1.3:
Heterogeneous Catalysts / 10.4.2:
Solid Acid Catalysts / 10.4.2.1:
Solid Base Catalysts / 10.4.2.2:
Enzyme-Catalyzed Transesterification Reactions / 10.4.3:
Supercritical Transesterification Processes / 10.5:
Alternative Processes for Biodiesel Production / 10.6:
Ultrasonic Processes / 10.6.1:
Microwave-Assisted Processes / 10.6.2:
Summary / 10.7:
Upgrading of Lipids to Hydrocarbon Fuels via (Hydro)deoxygenation / David Kubicka11:
Feedstocks / 11.1:
Chemistry / 11.3:
Technologies / 11.4:
Sulfided Catalysts / 11.5:
Metallic Catalysts / 11.5.2:
Metal Carbide, Nitride, and Phosphide Catalysts / 11.5.3:
Upgrading of Lipids to Fuel-like Hydrocarbons and Terminal Olefins via Decarbonylation/Decarboxylation / Ryan Loe and Eduardo Santillan-Jimenez and Mark Crocker11.6:
Lipid Feeds / 12.1:
deCOx Catalysts: Active Phases / 12.3:
deCOx Catalysts: Support Materials / 12.4:
Reaction Mechanism / 12.5:
Catalyst Deactivation / 12.7:
Conversion of Terpenes to Chemicals and Related Products / Anne E. Harman-Ware12.8:
Terpene Biosynthesis and Structure / 13.1:
Sources of Terpenes / 13.3:
Conifers and Other Trees / 13.3.1:
Essential Oils and Other Extracts / 13.3.2:
Isolation of Terpenes / 13.4:
Tapping and Extraction / 13.4.1:
Terpenes as a By-product of Pulping Processes / 13.4.2:
Historical Uses of Raw Terpenes / 13.5:
Adhesives and Turpentine / 13.5.1:
Flavors, Fragrances, Therapeutics, and Pharmaceutical Applications / 13.5.2:
Catalytic Methods for Conversion of Terpenes to Fine Chemicals and Materials / 13.6:
Homogeneous Processes / 13.6.1:
Hydration and Oxidation Reactions / 13.6.1.1:
Homogeneous Catalysis for the Epoxidation of Monoterpenes / 13.6.1.2:
Isomerizations / 13.6.1.3:
Production of Terpene Carbonates from CO2 and Epoxides / 13.6.1.4:
Polymers and Other Materials from Terpenes / 13.6.1.5:
"Click Chemistry" Routes for the Production of Materials and Medicinal Compounds from Terpenes / 13.6.1.6:
Heterogeneous Processes / 13.6.2:
Isomerization and Hydration of ¿-Pinene / 13.6.2.1:
Heterogeneous Catalysts for the Epoxidation of Monoterpenes / 13.6.2.2:
Isomerization of ¿-Pinene Oxide / 13.6.2.3:
Vitamins from Terpenes / 13.6.2.4:
Dehydrogenation and Hydrogenation Reactions of Terpenes / 13.6.2.5:
Conversion of Terpenes to Fuels / 13.6.2.6:
Conversion of Chitin to Nitrogen-containing Chemicals / Xi Chen and Ning Yan14:
Waste Shell Biorefinery / 14.1:
Production of Amines and Amides from Chitin Biomass / 14.2:
Sugar Amines/Amides / 14.2.1:
Furanic Amines/Amides / 14.2.2:
Polyol Amines/Amides / 14.2.3:
Production of N-heterocyclic Compounds from Chitin Biomass / 14.3:
Production of Carbohydrates and Acetic Acid from Chitin Biomass / 14.4:
Production of Advanced Products from Chitin Biomass / 14.5:
Conclusion / 14.6:
Index / Eduardo Santillan-Jimenez and Mark Crocker15:
Preface
Upgrading of Biomass via Catalytic Fast Pyrolysis (CFP) / Charles A. Mullen1:
Introduction / 1.1:
3.

電子ブック

EB
edited by Bin Zhu, Rizwan Raza, Liangdong Fan, Chunwen Sun
出版情報: Weinheim : Wiley-VCH, 2020  1 online resource (488 pages)
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Preface
Solid Oxide Fuel Cell with Ionic Conducting Electrolyte / Part I:
Introduction / Bin Zhu and Peter D. Lund1:
An Introduction to the Principles of Fuel Cells / 1.1:
Materials and Technologies / 1.2:
New Electrolyte Developments on LTSOFC / 1.3:
Beyond the State of the Art: The Electrolyte-Free Fuel Cell (EFFC) / 1.4:
Fundamental Issues / 1.4.1:
Beyond the SOFC / 1.5:
References
Solid-state Electrolytes for SOFC / Liangdong Fan2:
Single-Phase SOFC Electrolytes / 2.1:
Oxygen Ionic Conducting Electrolyte / 2.2.1:
Stabilized Zirconia / 2.2.1.1:
Doped Ceria / 2.2.1.2:
SrO- and MgO-Doped Lanthanum Gallates (LSGM) / 2.2.1.3:
Proton-Conducting Electrolyte and Mixed Ionic Conducting Electrolyte / 2.2.2:
Alternative New Electrolytes and Research Interests / 2.2.3:
Ion Conduction/Transportation in Electrolytes / 2.3:
Composite Electrolytes / 2.4:
Oxide-Oxide Electrolyte / 2.4.1:
Oxide-Carbonate Composite / 2.4.2:
Materials Fabrication / 2.4.2.1:
Performance and Stability Optimization / 2.4.2.2:
Other Oxide-Salt Composite Electrolytes / 2.4.3:
Ionic Conduction Mechanism Studies of Ceria-Carbonate Composite / 2.4.4:
NANOCOFC and Material Design Principle / 2.5:
Concluding Remarks / 2.6:
Acknowledgments
Cathodes for Solid Oxide Fuel Cell / Tianmin He and Qingjun Zhou and Fangjun Jin3:
Overview of Cathode Reaction Mechanism / 3.1:
Development of Cathode Materials / 3.3:
Perovskite Cathode Materials / 3.3.1:
Mn-Based Perovskite Cathodes / 3.3.1.1:
Co-Based Perovskite Cathodes / 3.3.1.2:
Fe-Based Perovskite Cathodes / 3.3.1.3:
Ni-Based Perovskite Cathodes / 3.3.1.4:
Double Perovskite Cathode Materials / 3.3.2:
Microstructure Optimization of Cathode Materials / 3.4:
Nanostructured Cathodes / 3.4.1:
Composite Cathodes / 3.4.2:
Summary / 3.5:
Anodes for Solid Oxide Fuel Cell / Chunwen Sun4:
Overview of Anode Reaction Mechanism / 4.1:
Basic Operating Principles of a SOFC / 4.2.1:
The Anode Three-Phase Boundary / 4.2.1.1:
Development of Anode Materials / 4.3:
Ni-YSZ Cermet Anode Materials / 4.3.1:
Alternative Anode Materials / 4.3.2:
Fluorite Anode Materials / 4.3.2.1:
Perovskite Anode Materials / 4.3.2.2:
Sulfur-Tolerant Anode Materials / 4.3.3:
Development of Kinetics, Reaction Mechanism, and Model of the Anode / 4.4:
Summary and Outlook / 4.5:
Design and Development of SOFC Stacks / Wanting Guan5:
Change of Cell Output Performance Under 2D Interface Contact / 5.1:
Design of 2D Interface Contact Mode / 5.2.1:
Variations of Cell Output Performance Under 2D Contact Mode / 5.2.2:
2D Interface Structure Improvements and Enhancement of Cell Output Performance / 5.2.3:
Contributions of 3D Contact in 2D Interface Contact / 5.2.4:
Mechanism of Performance Enhancement After the Transition from 2D to 3D Interface / 5.2.5:
Control Design of Transition from 2D to 3D Interface Contact and Their Quantitative Contribution Differentiation / 5.3:
Control Design of 2D and 3D Interface Contact / 5.3.1:
Quantitative Effects of 2D Contact on the Transient Output Performance of a Cell / 5.3.2:
Quantitative Effects of 2D Contact on the Steady-State Output Performance of the Cell / 5.3.3:
Quantitative Effects of 3D Contact on Cell Transient Performance / 5.3.4:
Quantitative Effects of 3D Contact on the Steady-State Performance of a Cell / 5.3.5:
Differences Between 2D and 3D Interface Contacts / 5.3.6:
Conclusions / 5.4:
Electrolyte-Free Fuel Cells: Materials, Technologies, and Working Principles / Part II:
Electrolyte-Free SOFCs: Materials, Technologies, and Working Principles / Bin Zhu and Liangdong Fan and Jung-Sik Kim and Peter D. Lund6:
Concept of the Electrolyte-Free Fuel Cell / 6.1:
SLFC Using the Ionic Conductor-based Electrolyte / 6.2:
Developments on Advanced SLFC / 6.3:
From SLFCs to Semiconductor-Ionic Fuel Cells (SIFCs) / 6.4:
The SLFC Working Principle / 6.5:
Remarks / 6.6:
Ceria Fluorite Electrolytes from Ionic to Mixed Electronic and Ionic Membranes / Baoyuan Wang and Liangdong Fan and Yanyan Liu and Bin Zhu7:
Doped Ceria as the Electrolyte for Intermediate Temperature SOFCs / 7.1:
Surface Doping for Low Temperature SOFCs / 7.3:
Non-doped Ceria for Advanced Low Temperature SOFCs / 7.4:
Charge Transfer in Oxide Solid Fuel Cells / Jing Shi and Sining Yun8:
Oxygen Diffusion in Perovskite Oxides / 8.1:
Oxygen Vacancy Formation / 8.1.1:
Oxygen Diffusion Mechanisms / 8.1.2:
Anisotropy Oxygen Transport in Layered Perovskites / 8.1.3:
Oxygen Transport in Ruddlesden-Popper (RP) Perovskites / 8.1.3.1:
Oxygen Transport in A-Site Ordered Double Perovskites / 8.1.3.2:
Oxygen Ion Diffusion at Grain Boundary / 8.1.4:
Factors Controlling Oxygen Migration Barriers in Perovskites / 8.1.5:
Proton Diffusion in Perovskite-Type Oxides / 8.2:
Proton Diffusion Mechanisms / 8.2.1:
Proton-Dopant Interaction / 8.2.2:
Influence of Dopants in A-site / 8.2.2.1:
Influence of Dopants in B-Stte / 8.2.2.2:
Long-range Proton Conduction Pathways in Perovskites / 8.2.3:
Hydrogen-Induced Insulation
Enhanced Ion Conductivity in Oxide Heterostructures / 8.3:
Enhanced Ionic Conduction by Strain / 8.3.1:
Enhanced Ionic Conductivity by Band Bending / 8.3.2:
Surface State-induced Band Bending / 8.3.2.1:
Band Bending in p-n Heterojunctions / 8.3.2.2:
p-n Hetero junction Structures in SOFC / 8.3.2.3:
Material Development II: Natural Material-based Composites for Electrolyte Layer-free Fuel Cells / Chen Xia and Yanyan Liu8.4:
Materials Development for EFFCs / 9.1:
Natural Materials as Potential Electrolytes / 9.1.2:
Industrial-grade Rare Earth for EFFCs / 9.2:
Rare-earth Oxide LCP / 9.2.1:
Semiconducting-Ionic Composite Based on LCP / 9.2.2:
LCP-LSCF / 9.2.2.1:
LCP-ZnO / 9.2.2.2:
Stability Operation and Schottky Junction of EFFC / 9.2.3:
Performance Stability / 9.2.3.1:
In Situ Schottky Junction Effect / 9.2.3.2:
Natural Hematite for EFFCs / 9.2.4:
Natural Hematite / 9.3.1:
Semiconducting-Ionic Composite Based on Hematite / 9.3.2:
Hematite-LSCF / 9.3.2.1:
Hematite/LCP-LSCF / 9.3.2.2:
Natural CuFe Oxide Minerals for EFFCs / 9.3.3:
Natural CuFe2O4 Mineral for EFFC / 9.4.1:
Natural Delafossite CuFeO2 for EFFC / 9.4.2:
Bio-derived Calcite for EFFC / 9.4.3:
Charge Transfer, Transportation, and Simulation / Muhammad Afzal and Mustafa Anwar and Muhammad I. Asghar and Peter D. Lund and Naveed Jhamat and Rizwan Raza and Bin Zhu9.5.1:
Physical Aspects / 10.1:
Electrochemical Aspects / 10.2:
Ionic Conduction Enhancement in Heterostructure Composites / 10.3:
Charge Transportation Mechanism and Coupling Effects / 10.4:
Surface and Interfacial State-Induced Superionic Conduction and Transportation / 10.5:
Ionic Transport Number Measurements / 10.6:
Determination of Electron and Ionic Conductivities in EFFCs / 10.7:
EIS Analysis / 10.8:
Semiconductor Band Effects on the Ionic Conduction Device Performance / 10.9:
Simulations / 10.10:
Electrolyte-Free Fuel Cell: Principles and Crosslink Research / Yan Wu and Liangdong Fan and Naveed Mushtaq and Bin Zhu and Muhammad Afzal and Muhammad Sajid and Rizwan Raza and Jung-Sik Kim and Wen-Feng Lin and Peter D. Lund11:
Fundamental Considerations of Fuel Cell Semiconductor Electrochemistry / 11.1:
Physics and Electrochemistry at Interfaces / 11.2.1:
Electrochemistry vs. Semiconductor Physics / 11.2.2:
Working Principle of Semiconductor-Based Fuel Cells and Crossing Link Sciences / 11.3:
Extending Applications by Coupling Devices / 11.4:
Final Remarks / 11.5:
Fuel Cells: From Technology to Applications / Part III:
Scaling Up Materials and Technology for SLFC / Kang Yuan and Zhigang Zhu and Muhammad Afzal and Bin Zhu12:
Single-Layer Fuel Cell (SLFC) Engineering Materials / 12.1:
Scaling Up Single-Layer Fuel Cell Devices: Tape Casting and Hot Pressing / 12.2:
Scaling Up Single-Layer Fuel Cell Devices: Thermal Spray Coating Technology / 12.3:
Traditional Plasma Spray Coating Technology / 12.3.1:
New Developed Low-Pressure Plasma Spray (LPPS) Coating Technology / 12.3.2:
Short Stack / 12.4:
SLFC Cells / 12.4.1:
Bipolar Plate Design / 12.4.2:
Sealing and Sealant-Free Short Stack / 12.4.3:
Tests and Evaluations / 12.5:
Durability Testing / 12.6:
A Case Study for the Cell Degradation Mechanism / 12.7:
Continuous Efforts and Future Developments / 12.8:
Planar SOFC Stack Design and Development / Shaorong Wang and Yixiang Shi and Naveed Mushtaq and Bin Zhu12.9:
Internal Manifold and External Manifold / 13.1:
Interface Between an Interconnect Plate and a Single Cell / 13.2:
Antioxidation Coating of the Interconnect Plate / 13.3:
Design the Flow Field of Interconnect Plate / 13.4:
Mathematical Simulation / 13.4.1:
Effect of Co-flow, Crossflow, and Counterflow / 13.4.2:
Air Flow Distribution Between Layers in a Stack / 13.4.3:
The Importance of Sealing / 13.5:
Thermal Cycling of the Sealing / 13.5.1:
Durability of Sealing / 13.5.2:
The Life of the Stack: The Chemical Problems on the Interface / 13.6:
Toward Market Products / 13.7:
Energy System Integration and Future Perspectives / Ghazanfar Abbas and Muhammad Ali Babar and Fida Hussain and Rizwan Raza13.8:
Solar Cell and Fuel Cell / 14.1:
Fuel Cell-Solar Cell Integration / 14.2:
Solar Electrolysis-Fuel Cell Integration / 14.3:
Fuel Cell-Biomass Integration / 14.4:
The Fuel Cell System Modeling Using Biogas / 14.5:
Activation Loss / 14.5.1:
Ohmic Loss / 14.5.2:
Concentration Voltage Loss / 14.5.3:
The Fuel Cell System Efficiency (Heating and Electrical) / 14.6:
The Effect of Different Temperatures on System Efficiency / 14.6.1:
The Fuel Utilization Factor and Efficiencies of the System / 14.6.2:
The System Efficiencies and Operating Pressure / 14.6.3:
Integrated New Clean Energy System / 14.7:
Index / 14.8:
Preface
Solid Oxide Fuel Cell with Ionic Conducting Electrolyte / Part I:
Introduction / Bin Zhu and Peter D. Lund1:
4.

電子ブック

EB
Gang Wang, Hou Chengyi, Wang Hongzhi
出版情報: Wiley Online Library - AutoHoldings Books , John Wiley & Sons, Inc., 2020
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Preface
Sensing / Part I:
Wearable Organic Nano-sensors / Wei Huong and Liangwen Feng and Gang Wang and Elsa Reichmanis1:
Introduction / 1.1:
Wearable Organic Sensors Based on Different Device Architectures / 1.2:
Resistor-Based Sensors / 1.2.1:
Definitions and Important Parameters / 1.2.1.1:
Materials and Applications / 1.2.1.2:
Organic Field-Effect Transistor Based Sensors / 1.2.2:
Strategy and Applications / 1.2.2.1:
Electrochemical Sensors / 1.2.3:
Diode-Based Sensors / 1.2.3.1:
Other Devices and System Integration / 1.2.4.1:
Summary and Perspective / 1.3:
References
Stimuli-Responsive Electronic Skins / Zhouyue Lei and Peiyi Wu2:
Materials for Electronic Skins / 2.1:
Liquid Metals / 2.2.1:
Hydrogels / 2.2.2:
Ionogels / 2.2.3:
Elastomers / 2.2.4:
Conductive Polymers / 2.2.5:
Inorganic Materials / 2.2.6:
Stimuli-Responsive Behaviors / 2.3:
Electrical Signals in Response to Environmental Stimuli / 2.3.1:
Stimuli-Responsive Self-healing / 2.3.2:
Stimuli-Responsive Optical Appearances / 2.3.3:
Stimuli-Responsive Actuations / 2.3.4:
Improved Processability Based on Stimuli-Responsive Behaviors / 2.3.5:
Understanding the Mechanism of Stimuli-Responsive Materials Applied for Electronic Skins / 2.4:
Conclusion / 2.5:
Flexible Thermoelectrics and Thermoelectric Textiles / Fei Jiao3:
Thermoelectricity and Thermoelectric Materials / 3.1:
Thermoelectric Generators / 3.3:
Wearable Thermoelectric Generators for Smart Clothing / 3.4:
Flexible Thermoelectrics / 3.4.1:
Inorganic Thermoelectric Materials Related / 3.4.1.1:
Organic Thermoelectric Materials Related / 3.4.1.2:
Carbon-Based Thermoelectric Materials Related / 3.4.1.3:
Fiber and Textile Related Thermoelectrics / 3.4.2:
Prospects and Challenges / 3.5:
Energy / Part II:
Textile Triboelectric Nanogenerators for Energy Harvesting / Xiong Pu4:
Fundamentals of Triboelectric Nanogenerators (TENGs) / 4.1:
Theoretical Origin of TENGs / 4.2.1:
Four Working Modes / 4.2.2:
Materials for TENGs / 4.2.3:
Progresses in Textile TENGs / 4.3:
Materials for Textile TENGs / 4.3.1:
Fabrication Processes for Textile TENGs / 4.3.2:
Structures of Textile TENGs / 4.3.3:
ID Fiber TENGs / 4.3.3.1:
2D Fabric TENGs / 4.3.3.2:
3D Fabric TENGs / 4.3.3.3:
Washing Capability / 4.3.4:
Self-charging Power Textiles / 4.3.5:
Conclusions and Perspectives / 4.4:
Flexible and Wearable Solar Cells and Supercapacitors / Kai Yuan and Ting Hu and Yiwang Chen5:
Flexible and Wearable Solar Cells / 5.1:
Flexible and Wearable Dye-Sensitized Solar Cells / 5.2.1:
Flexible and Wearable Polymer Solar Cells / 5.2.2:
Flexible and Wearable Perovskite Solar Cells / 5.2.3:
Flexible and Wearable Supercapacitors / 5.2.4:
Flexible and Wearable Electric Double-Layer Capacitors (EDLCs) / 5.2.5:
Flexible and Wearable Pseudocapacitor / 5.2.6:
Integrated Solar Cells and Supercapacitors / 5.2.7:
Conclusions and Outlook / 5.3:
Acknowledgments
Flexible and Wearable Lithium-Ion Batteries / Zhiwei Zhang and Peng Wang and Xianguang Miao and Peng Zhang and Longwei Yin6:
Typical Lithium-Ion Batteries / 6.1:
Electrode Materials for Flexible Lithium-Ion Batteries / 6.3:
Three-Dimensional (3D) Electrodes / 6.3.1:
Two-Dimensional (2D) Electrodes / 6.3.2:
Conductive Substrate-Based Electrodes / 6.3.2.1:
Freestanding Film-Based Electrodes / 6.3.2.2:
Graphene Papers / 6.3.2.3:
CNT Papers / 6.3.2.4:
Fabrication of Carbon Films by Vacuum Filtration Process / 6.3.2.5:
Fabrication of Carbon Nanofiber Films by Electrospinning / 6.3.2.6:
Fabrication of Carbon Films by Vapor-Phase Polymerization / 6.3.2.7:
One-Dimensional (1D) Electrodes / 6.3.3:
Flexible Lithium-Ion Batteries Based on Electrolytes / 6.4:
Liquid-State Electrolytes / 6.4.1:
Aprotic Organic Solvent / 6.4.1.1:
Lithium Salts / 6.4.1.2:
Additives / 6.4.1.3:
Solid-State Electrolytes / 6.4.2:
Inorganic Electrolytes / 6.4.2.1:
Organic Electrolytes / 6.4.2.2:
Organic/Inorganic Hybrid Electrolytes / 6.4.2.3:
Inactive Materials and Components of Flexible LIBs / 6.5:
Separators / 6.5.1:
Types of Separators / 6.5.1.1:
Physical and Chemical Properties of Separators / 6.5.1.2:
Manufacture of Separators / 6.5.1.3:
Casing/Packaging / 6.5.2:
Casing/Package Components / 6.5.2.1:
Casing/Packaging Structure / 6.5.2.2:
Current Collectors / 6.5.3:
Electrode Additive Materials / 6.5.4:
Binders / 6.5.4.1:
Conductive Additives / 6.5.4.2:
Conclusions and Prospects / 6.6:
Interacting / Part III:
Thermal and Humidity Management for Next-Generation Textiles / Junxing Meng and Chengyi Hou and Chenhong Zhang and Qinghong Zhang and Yaogang Li and Hongzhi Wang7:
Passive Smart Materials / 7.1:
Energy-Harvesting Materials / 7.3:
Active Smart Materials / 7.4:
Functionalization of Fiber Materials for Washable Smart Wearable Textiles / Yunjie Yin and Yan Xu and Chaoxia Wang7.5:
Conductive Textiles / 8.1:
Waterproof Conductive Textiles / 8.1.2:
Washable Conductive Textiles / 8.1.3:
Evaluation of Washable Conductive Textiles / 8.1.4:
Fiber Materials Functionalization for Conductivity / 8.2:
Conductive Fiber Substrates Based on Polymer Materials / 8.2.1:
Dip Coating / 8.2.1.1:
Graft Modification / 8.2.1.2:
In Situ Chemical Polymerization / 8.2.1.3:
Electrochemical Polymerization / 8.2.1.4:
In Situ Vapor Phase Polymerization / 8.2.1.5:
Conductive Fiber Substrates Based on Metal Materials / 8.2.2:
Electroless Plating / 8.2.2.1:
Metal Conductive Ink Printing / 8.2.2.2:
Conductive Fiber Substrates Based on Carbon Material / 8.2.3:
Vacuum Filtration / 8.2.3.1:
Printing / 8.2.3.2:
Dyeing / 8.2.3.4:
Ultrasonic Depositing / 8.2.3.5:
Brushing Coating / 8.2.3.6:
Conductive Fiber Substrates Based on Graphene Composite Materials / 8.2.4:
In Situ Polymerization / 8.2.4.1:
Waterproof Modification for Conductive Fiber Substrates / 8.3:
Dip-Coating Method / 8.3.1:
Sol-Gel Method / 8.3.2:
Chemical Vapor Deposition / 8.3.3:
Washing Evaluations of Conductive Textiles / 8.4:
Conclusions / 8.5:
Flexible Microfluidics for Wearable Electronics / Dachao Li and Haixia Yu and Zhihua Pu and Xiaochen Lai and Chengtao Sun and Hao Wu and Xingguo Zhang9:
Materials / 9.1:
Fabrication Technologies / 9.3:
Layer Transfer and Lamination / 9.3.1:
Soft Lithography / 9.3.2:
Inkjet Printing / 9.3.3:
3D Printing / 9.3.4:
3D Printing Sacrificial Structures / 9.3.4.1:
3D Printing Templates / 9.3.4.2:
Fabrication of Open-Surface Microfluidics / 9.3.5:
Fabrication of Paper-Based Microfluidic Device / 9.3.5.1:
Fabrication of Textile-Based Microfluidic Device / 9.3.5.2:
Applications / 9.4:
Wearable Microfluidics for Sweat-Based Biosensing / 9.4.1:
Wearable Microfluidics for ISF-Based Biosensing / 9.4.2:
Wearable Microfluidics for Motion Sensing / 9.4.3:
Other Flexible Microfluidics / 9.4.4:
Soft Robotics / 9.4.4.1:
Drug Delivery / 9.4.4.2:
Implantable Devices / 9.4.4.3:
Flexible Display / 9.4.4.4:
Challenges / 9.5:
Integrating and Connecting / Part IV:
Piezoelectric Materials and Devices Based Flexible Bio-integrated Electronics / Xinge Yu10:
Piezoelectric Materials / 10.1:
Piezoelectric Devices for Biomedical Applications / 10.3:
Flexible and Printed Electronics for Smart Clothes / Yu Jiang and Nan Zhu10.4:
Printing Technology / 11.1:
Non-template Printing / 11.2.1:
Template-Based Printing / 11.2.2:
Flexible Substrates / 11.3:
Commercially Available Polymers / 11.3.1:
Polyethylene Terephthalate (PET) / 11.3.1.1:
Polydimethylsiloxane (PDMS) / 11.3.1.2:
Polyimide (PI) / 11.3.1.3:
Polyurethane (PU) / 11.3.1.4:
Others / 11.3.1.5:
Printing Papers / 11.3.2:
Tattoo Papers / 11.3.3:
Fiber Textiles / 11.3.4:
Application / 11.3.5:
Wearable Sensors/Biosensors / 11.4.1:
Noninvasive Biofuel Cells / 11.4.2:
Wearable Energy Storage Devices / 11.4.3:
Prospects / 11.5:
Flexible and Wearable Electronics: from Lab to Fab / Yuanyuan Bai and Xianqing Yang and Lianhui Li and Tie Li and Ting Zhang12:
Substrates / 12.1:
Functional Materials / 12.2.2:
Printing Technologies / 12.3:
Jet Printing / 12.3.1:
Aerosol Jet Printing / 12.3.1.1:
Electrohydrodynamic Jet (e-Jet) Printing / 12.3.1.3:
Screen Printing / 12.3.2:
Other Printing Techniques / 12.3.3:
Flexible and Wearable Electronic Products / 12.4:
Flexible Force Sensors / 12.4.1:
Paper Battery / 12.4.2:
Flexible Solar Cell / 12.4.3:
Strategy Toward Smart Clothing / 12.4.4:
Materials and Processes for Stretchable and Wearable e-Textile Devices / Binghao Wang and Antonio Facchetti12.6:
Materials for e-Textiles / 13.1:
Conducting Materials / 13.2.1:
Metal Nanomaterials / 13.2.1.1:
Carbon Nanomaterials / 13.2.1.2:
Conducting Polymers / 13.2.1.3:
Passive Textile Materials / 13.2.2:
Device Applications / 13.3:
Interconnects and Electrodes / 13.3.1:
Strain Sensors / 13.3.2:
Heaters / 13.3.3:
Supercapacitors / 13.3.4:
Energy Generators / 13.3.5:
Triboelectric Generators / 13.3.5.1:
Summary and Perspectives / 13.4:
Index
Preface
Sensing / Part I:
Wearable Organic Nano-sensors / Wei Huong and Liangwen Feng and Gang Wang and Elsa Reichmanis1:
5.

図書

図書
Rosette M. Roat-Malone
出版情報: Hoboken, N.J. : John Wiley & Sons, c2020  xxii, 328 p. ; 23 cm
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Preface
Acknowledgments
Biography
About the Companion Page
Inorganic Chemistry And Biochemistry Essentials / 1:
Introduction / 1.1:
Essential Chemical Elements / 1.2:
Inorganic Chemistry Basics / 1.3:
Electronic and Geometric Structures of Metals in Biological Systems / 1.4:
Thermodynamics and Kinetics / 1.5:
Bioorganometallic Chemistry / 1.6:
Inorganic Chemistry Conclusions / 1.7:
Introduction to Biochemistry / 1.8:
Proteins / 1.9:
Amino Acid Building Blocks / 1.9.1:
Protein Structure / 1.9.2:
Protein Function, Enzymes, and Enzyme Kinetics / 1.9.3:
DNA and RNA Building Blocks / 1.10:
DNA and RNA Molecular Structures / 1.10.1:
Transmission of Genetic Information / 1.10.2:
Genetic Mutations and Site-Directed Mutagenesis / 1.10.3:
Genes and Cloning / 1.10.4:
Genomics and the Human Genome / 1.10.5:
CRISPR / 1.10.6:
A Descriptive Example: Electron Transport Through DNA / 1.11:
Cyclic Voltammetry / 1.11.1:
Summary and Conclusions / 1.12:
Questions and Thought Problems / 1.13:
References
Computer Hardware, Software, Computational Chemistry Methods / 2:
Introduction to Computer-Based Methods / 2.1:
Computer Hardware / 2.2:
Computer Software for Chemistry / 2.3:
Chemical Drawing Programs / 2.3.1:
Visualization Programs / 2.3.2:
Computational Chemistry Software / 2.3.3:
Molecular Dynamics (MD) Software / 2.3.3.1:
Mathematical and Graphing Software / 2.3.3.2:
Molecular Mechanics (MM), Molecular Modeling, and Molecular Dynamics (MD) / 2.4:
Quantum Mechanics-Based Computational Methods / 2.5:
Ab-Initio Methods / 2.5.1:
Semiempirical Methods / 2.5.2:
Density Functional Theory and Examples / 2.5.3:
Starting with Schrödinger / 2.5.3.1:
Density Functional Theory (DFT) / 2.5.3.2:
Basis Sets / 2.5.3.3:
DFT Applications / 2.5.3.4:
Quantum Mechanics/Molecular Mechanics (QM/MM) Methods / 2.5.4:
Conclusions on Hardware, Software, and Computational Chemistry / 2.6:
Databases, Visualization Tools, Nomenclature, and other Online Resources / 2.7:
Important Metal Centers In Proteins / 2.8:
Iron Centers in Myoglobin and Hemoglobin / 3.1:
Structure and Function as Determined by X-ray Crystallography and Nuclear Magnetic Resonance / 3.1.1:
Cryo-Electron Microscopy and Hemoglobin Structure/Function / 3.1.3:
Cryo-Electron Microscopy Techniques / 3.1.3.1:
Structures Determined Using Cryo-Electron Microscopy / 3.1.3.3:
Model Compounds / 3.1.4:
Blood Substitutes / 3.1.5:
Iron Centers in Cytochromes / 3.2:
Cytochrome c Oxidase / 3.2.1:
Cytochrome c Oxidase (CcO) Structural Studies / 3.2.2:
Cytochrome c Oxidase (CcO) Catalytic Cycle and Energy Considerations / 3.2.3:
Proton Channels in Cytochrome c Oxidase / 3.2.4:
Cytochrome c Oxidase Model Compounds / 3.2.5:
Iron-Sulfur Clusters in Nitrogenase / 3.3:
Nitrogenase Structure and Catalytic Mechanism / 3.3.1:
Mechanism of Dinitrogen (N2) Reduction / 3.3.3:
Substrate Pathways into Nitrogenase / 3.3.4:
Nitrogenase Model Compounds / 3.3.5:
Functional Nitrogenase Models / 3.3.5.1:
Structural Nitrogenase Models / 3.3.5.2:
Copper and Zinc in Superoxide Dismutase / 3.4:
Superoxide Dismutase Structure and Mechanism of Catalytic Activity / 3.4.1:
A Copper Zinc Superoxide Dismutase Model Compound / 3.4.3:
Methane Monooxygenase / 3.5:
Soluble Methane Monooxygenase / 3.5.1:
Particulate Methane Monooxygenase / 3.5.3:
Hydrogenases, Carbonic Anhydrases, Nitrogen Cycle Enzymes / 3.6:
Hydrogenases / 4.1:
[NiFe]-hydrogenases / 4.2.1:
[NiFe]-hydrogenase Model Compounds / 4.2.2.1:
[FeFe]-hydrogenases / 4.2.3:
[FeFe]-Hydrogenase Model Compounds / 4.2.3.1:
[Fe]-hydrogenases / 4.2.4:
[Fe]-Hydrogenase Model Compounds / 4.2.4.1:
Carbonic Anhydrases / 4.3:
Carbonic Anhydrase Inhibitors / 4.3.1:
Nitrogen Cycle Enzymes / 4.4:
Nitric Oxide synthase / 4.4.1:
Nitric Oxide Synthase Structure / 4.4.2.1:
Nitric Oxide Synthase Inhibitors / 4.4.2.3:
Nitrite Reductase / 4.4.3:
Reduction of Nitrite Ion to Ammonium Ion / 4.4.3.1:
Reduction of Nitrite Ion to Nitric Oxide / 4.4.3.3:
Nanobioinorganic Chemistry / 4.5:
Introduction to Nanomaterials / 5.1:
Analytical Methods / 5.2:
Microscopy / 5.2.1:
Scanning Electron Microscopy (SEM) / 5.2.1.1:
Transmission Electron Microscopy (TEM) / 5.2.1.2:
Scanning Transmission Electron Microscopy (STEM) / 5.2.1.3:
Cryo-Electron Microscopy / 5.2.1.4:
Scanning Probe Microscopy (SPM) / 5.2.1.5:
Atomic Force Microscopy (AFM) / 5.2.1.6:
Super-Resolution Microscopy and DNA-PAINT / 5.2.1.7:
Förster Resonance Energy Transfer (FRET) / 5.2.2:
DNA Origami / 5.3:
Metallized DNA Nanomaterials / 5.4:
DNA-Coated Metal Electrodes / 5.4.1:
Plasmonics and DNA / 5.4.3:
Bioimaging with Nanomaterials, Nanomedicine, and Cytotoxicity / 5.5:
Imaging with Nanomaterials / 5.5.1:
Bioimaging using Quantum Dots (QD) / 5.5.3:
Nanoparticles in Therapeutic Nanomedicine / 5.5.4:
Clinical Nanomedicine / 5.5.4.1:
Some Drugs Formulated into Nanomaterials for Cancer Treatment: Cisplatinum, Platinum(IV) Prodrugs, and Doxorubicin / 5.5.4.2:
Theranostics / 5.6:
Nanoparticle Toxicity / 5.7:
Metals In Medicine, Disease States, Drug Development / 5.8:
Platinum Anticancer Agents / 6.1:
Cisplatin / 6.1.1:
Cisplatin Toxicity / 6.1.1.1:
Mechanism of Cisplatin Activity / 6.1.1.2:
Carboplatin (Paraplatin) / 6.1.2:
Oxaliplatin / 6.1.3:
Other cis-Platinum(II) Compounds / 6.1.4:
Nedaplatin / 6.1.4.1:
Lobaplatin / 6.1.4.2:
Heptaplatin / 6.1.4.3:
Antitumor Active Trans Platinum compounds / 6.1.5:
Platinum Drug Resistance / 6.1.6:
Combination Therapies: Platinum-Containing Drugs with Other Antitumor Compounds / 6.1.7:
Platinum(IV) Antitumor Drugs / 6.1.8:
Satraplatin / 6.1.8.1:
Ormaplatin / 6.1.8.2:
Iproplatin, JM9, CHIP / 6.1.8.3:
Platinum(TV) Prodrugs / 6.1.9:
Multitargeted Platinum(IV) Prodrugs / 6.1.9.1:
Platinum(IV) Prodrugs Delivered via Nanoparticles / 6.1.9.2:
Ruthenium Compounds as Anticancer Agents / 6.2:
Ruthenium(III) Anticancer Agents / 6.2.1:
Ruthenium(II) Anticancer Agents / 6.2.2:
Mechanism of Ruthenium(II) Anticancer Agent Activity / 6.2.3:
Ruthenium Compounds Tested for Antitumor Activity / 6.2.4:
Iridium and Osmium Antitumor Agents / 6.3:
Other Antitumor Agents / 6.4:
Gold Complexes / 6.4.1:
Titanium Complexes / 6.4.2:
Copper Complexes / 6.4.3:
Bismuth Derivatives as Antibacterials / 6.5:
Disease States, Drug Discovery, and Treatments / 6.6:
Superoxide Dismutases (SOD) in Disease States / 6.6.1:
Amyotrophic Lateral Sclerosis / 6.6.2:
Wilson's and Menkes Disease / 6.6.3:
Alzheimer's disease / 6.6.4:
Role of Amyloid ß Protein / 6.6.4.1:
Interactions of Aß Peptides with Metals / 6.6.4.2:
Alzheimer's Disease Treatments / 6.6.4.3:
Other Disease States Involving Metals / 6.7:
Copper and Zinc Ions and Cataract Formation / 6.7.1:
As2O3, used in the Treatment of Acute Promyelocytic Leukemia (APL) / 6.7.2:
Vanadium-based Type 2 Diabetes Drugs / 6.7.3:
Index / 6.8:
Preface
Acknowledgments
Biography
6.

図書

図書
International Conference on Microbiome Engineering ; American Institute of Chemical Engineers
出版情報: New York : AIChE , Red Hook, NY : Printed from e-media with permission by Curran Associates, 2020. c2019  [3], 40, [2] p. ; 28 cm
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7.

電子ブック

EB
Zhu, Fan Liangdong, Raza Rizwan, Sun Chunwen
出版情報: Wiley Online Library - AutoHoldings Books , John Wiley & Sons, Inc., 2020
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目次情報: 続きを見る
Preface
Solid Oxide Fuel Cell with Ionic Conducting Electrolyte / Part I:
Introduction / Bin Zhu and Peter D. Lund1:
An Introduction to the Principles of Fuel Cells / 1.1:
Materials and Technologies / 1.2:
New Electrolyte Developments on LTSOFC / 1.3:
Beyond the State of the Art: The Electrolyte-Free Fuel Cell (EFFC) / 1.4:
Fundamental Issues / 1.4.1:
Beyond the SOFC / 1.5:
References
Solid-state Electrolytes for SOFC / Liangdong Fan2:
Single-Phase SOFC Electrolytes / 2.1:
Oxygen Ionic Conducting Electrolyte / 2.2.1:
Stabilized Zirconia / 2.2.1.1:
Doped Ceria / 2.2.1.2:
SrO- and MgO-Doped Lanthanum Gallates (LSGM) / 2.2.1.3:
Proton-Conducting Electrolyte and Mixed Ionic Conducting Electrolyte / 2.2.2:
Alternative New Electrolytes and Research Interests / 2.2.3:
Ion Conduction/Transportation in Electrolytes / 2.3:
Composite Electrolytes / 2.4:
Oxide-Oxide Electrolyte / 2.4.1:
Oxide-Carbonate Composite / 2.4.2:
Materials Fabrication / 2.4.2.1:
Performance and Stability Optimization / 2.4.2.2:
Other Oxide-Salt Composite Electrolytes / 2.4.3:
Ionic Conduction Mechanism Studies of Ceria-Carbonate Composite / 2.4.4:
NANOCOFC and Material Design Principle / 2.5:
Concluding Remarks / 2.6:
Acknowledgments
Cathodes for Solid Oxide Fuel Cell / Tianmin He and Qingjun Zhou and Fangjun Jin3:
Overview of Cathode Reaction Mechanism / 3.1:
Development of Cathode Materials / 3.3:
Perovskite Cathode Materials / 3.3.1:
Mn-Based Perovskite Cathodes / 3.3.1.1:
Co-Based Perovskite Cathodes / 3.3.1.2:
Fe-Based Perovskite Cathodes / 3.3.1.3:
Ni-Based Perovskite Cathodes / 3.3.1.4:
Double Perovskite Cathode Materials / 3.3.2:
Microstructure Optimization of Cathode Materials / 3.4:
Nanostructured Cathodes / 3.4.1:
Composite Cathodes / 3.4.2:
Summary / 3.5:
Anodes for Solid Oxide Fuel Cell / Chunwen Sun4:
Overview of Anode Reaction Mechanism / 4.1:
Basic Operating Principles of a SOFC / 4.2.1:
The Anode Three-Phase Boundary / 4.2.1.1:
Development of Anode Materials / 4.3:
Ni-YSZ Cermet Anode Materials / 4.3.1:
Alternative Anode Materials / 4.3.2:
Fluorite Anode Materials / 4.3.2.1:
Perovskite Anode Materials / 4.3.2.2:
Sulfur-Tolerant Anode Materials / 4.3.3:
Development of Kinetics, Reaction Mechanism, and Model of the Anode / 4.4:
Summary and Outlook / 4.5:
Design and Development of SOFC Stacks / Wanting Guan5:
Change of Cell Output Performance Under 2D Interface Contact / 5.1:
Design of 2D Interface Contact Mode / 5.2.1:
Variations of Cell Output Performance Under 2D Contact Mode / 5.2.2:
2D Interface Structure Improvements and Enhancement of Cell Output Performance / 5.2.3:
Contributions of 3D Contact in 2D Interface Contact / 5.2.4:
Mechanism of Performance Enhancement After the Transition from 2D to 3D Interface / 5.2.5:
Control Design of Transition from 2D to 3D Interface Contact and Their Quantitative Contribution Differentiation / 5.3:
Control Design of 2D and 3D Interface Contact / 5.3.1:
Quantitative Effects of 2D Contact on the Transient Output Performance of a Cell / 5.3.2:
Quantitative Effects of 2D Contact on the Steady-State Output Performance of the Cell / 5.3.3:
Quantitative Effects of 3D Contact on Cell Transient Performance / 5.3.4:
Quantitative Effects of 3D Contact on the Steady-State Performance of a Cell / 5.3.5:
Differences Between 2D and 3D Interface Contacts / 5.3.6:
Conclusions / 5.4:
Electrolyte-Free Fuel Cells: Materials, Technologies, and Working Principles / Part II:
Electrolyte-Free SOFCs: Materials, Technologies, and Working Principles / Bin Zhu and Liangdong Fan and Jung-Sik Kim and Peter D. Lund6:
Concept of the Electrolyte-Free Fuel Cell / 6.1:
SLFC Using the Ionic Conductor-based Electrolyte / 6.2:
Developments on Advanced SLFC / 6.3:
From SLFCs to Semiconductor-Ionic Fuel Cells (SIFCs) / 6.4:
The SLFC Working Principle / 6.5:
Remarks / 6.6:
Ceria Fluorite Electrolytes from Ionic to Mixed Electronic and Ionic Membranes / Baoyuan Wang and Liangdong Fan and Yanyan Liu and Bin Zhu7:
Doped Ceria as the Electrolyte for Intermediate Temperature SOFCs / 7.1:
Surface Doping for Low Temperature SOFCs / 7.3:
Non-doped Ceria for Advanced Low Temperature SOFCs / 7.4:
Charge Transfer in Oxide Solid Fuel Cells / Jing Shi and Sining Yun8:
Oxygen Diffusion in Perovskite Oxides / 8.1:
Oxygen Vacancy Formation / 8.1.1:
Oxygen Diffusion Mechanisms / 8.1.2:
Anisotropy Oxygen Transport in Layered Perovskites / 8.1.3:
Oxygen Transport in Ruddlesden-Popper (RP) Perovskites / 8.1.3.1:
Oxygen Transport in A-Site Ordered Double Perovskites / 8.1.3.2:
Oxygen Ion Diffusion at Grain Boundary / 8.1.4:
Factors Controlling Oxygen Migration Barriers in Perovskites / 8.1.5:
Proton Diffusion in Perovskite-Type Oxides / 8.2:
Proton Diffusion Mechanisms / 8.2.1:
Proton-Dopant Interaction / 8.2.2:
Influence of Dopants in A-site / 8.2.2.1:
Influence of Dopants in B-Stte / 8.2.2.2:
Long-range Proton Conduction Pathways in Perovskites / 8.2.3:
Hydrogen-Induced Insulation
Enhanced Ion Conductivity in Oxide Heterostructures / 8.3:
Enhanced Ionic Conduction by Strain / 8.3.1:
Enhanced Ionic Conductivity by Band Bending / 8.3.2:
Surface State-induced Band Bending / 8.3.2.1:
Band Bending in p-n Heterojunctions / 8.3.2.2:
p-n Hetero junction Structures in SOFC / 8.3.2.3:
Material Development II: Natural Material-based Composites for Electrolyte Layer-free Fuel Cells / Chen Xia and Yanyan Liu8.4:
Materials Development for EFFCs / 9.1:
Natural Materials as Potential Electrolytes / 9.1.2:
Industrial-grade Rare Earth for EFFCs / 9.2:
Rare-earth Oxide LCP / 9.2.1:
Semiconducting-Ionic Composite Based on LCP / 9.2.2:
LCP-LSCF / 9.2.2.1:
LCP-ZnO / 9.2.2.2:
Stability Operation and Schottky Junction of EFFC / 9.2.3:
Performance Stability / 9.2.3.1:
In Situ Schottky Junction Effect / 9.2.3.2:
Natural Hematite for EFFCs / 9.2.4:
Natural Hematite / 9.3.1:
Semiconducting-Ionic Composite Based on Hematite / 9.3.2:
Hematite-LSCF / 9.3.2.1:
Hematite/LCP-LSCF / 9.3.2.2:
Natural CuFe Oxide Minerals for EFFCs / 9.3.3:
Natural CuFe2O4 Mineral for EFFC / 9.4.1:
Natural Delafossite CuFeO2 for EFFC / 9.4.2:
Bio-derived Calcite for EFFC / 9.4.3:
Charge Transfer, Transportation, and Simulation / Muhammad Afzal and Mustafa Anwar and Muhammad I. Asghar and Peter D. Lund and Naveed Jhamat and Rizwan Raza and Bin Zhu9.5.1:
Physical Aspects / 10.1:
Electrochemical Aspects / 10.2:
Ionic Conduction Enhancement in Heterostructure Composites / 10.3:
Charge Transportation Mechanism and Coupling Effects / 10.4:
Surface and Interfacial State-Induced Superionic Conduction and Transportation / 10.5:
Ionic Transport Number Measurements / 10.6:
Determination of Electron and Ionic Conductivities in EFFCs / 10.7:
EIS Analysis / 10.8:
Semiconductor Band Effects on the Ionic Conduction Device Performance / 10.9:
Simulations / 10.10:
Electrolyte-Free Fuel Cell: Principles and Crosslink Research / Yan Wu and Liangdong Fan and Naveed Mushtaq and Bin Zhu and Muhammad Afzal and Muhammad Sajid and Rizwan Raza and Jung-Sik Kim and Wen-Feng Lin and Peter D. Lund11:
Fundamental Considerations of Fuel Cell Semiconductor Electrochemistry / 11.1:
Physics and Electrochemistry at Interfaces / 11.2.1:
Electrochemistry vs. Semiconductor Physics / 11.2.2:
Working Principle of Semiconductor-Based Fuel Cells and Crossing Link Sciences / 11.3:
Extending Applications by Coupling Devices / 11.4:
Final Remarks / 11.5:
Fuel Cells: From Technology to Applications / Part III:
Scaling Up Materials and Technology for SLFC / Kang Yuan and Zhigang Zhu and Muhammad Afzal and Bin Zhu12:
Single-Layer Fuel Cell (SLFC) Engineering Materials / 12.1:
Scaling Up Single-Layer Fuel Cell Devices: Tape Casting and Hot Pressing / 12.2:
Scaling Up Single-Layer Fuel Cell Devices: Thermal Spray Coating Technology / 12.3:
Traditional Plasma Spray Coating Technology / 12.3.1:
New Developed Low-Pressure Plasma Spray (LPPS) Coating Technology / 12.3.2:
Short Stack / 12.4:
SLFC Cells / 12.4.1:
Bipolar Plate Design / 12.4.2:
Sealing and Sealant-Free Short Stack / 12.4.3:
Tests and Evaluations / 12.5:
Durability Testing / 12.6:
A Case Study for the Cell Degradation Mechanism / 12.7:
Continuous Efforts and Future Developments / 12.8:
Planar SOFC Stack Design and Development / Shaorong Wang and Yixiang Shi and Naveed Mushtaq and Bin Zhu12.9:
Internal Manifold and External Manifold / 13.1:
Interface Between an Interconnect Plate and a Single Cell / 13.2:
Antioxidation Coating of the Interconnect Plate / 13.3:
Design the Flow Field of Interconnect Plate / 13.4:
Mathematical Simulation / 13.4.1:
Effect of Co-flow, Crossflow, and Counterflow / 13.4.2:
Air Flow Distribution Between Layers in a Stack / 13.4.3:
The Importance of Sealing / 13.5:
Thermal Cycling of the Sealing / 13.5.1:
Durability of Sealing / 13.5.2:
The Life of the Stack: The Chemical Problems on the Interface / 13.6:
Toward Market Products / 13.7:
Energy System Integration and Future Perspectives / Ghazanfar Abbas and Muhammad Ali Babar and Fida Hussain and Rizwan Raza13.8:
Solar Cell and Fuel Cell / 14.1:
Fuel Cell-Solar Cell Integration / 14.2:
Solar Electrolysis-Fuel Cell Integration / 14.3:
Fuel Cell-Biomass Integration / 14.4:
The Fuel Cell System Modeling Using Biogas / 14.5:
Activation Loss / 14.5.1:
Ohmic Loss / 14.5.2:
Concentration Voltage Loss / 14.5.3:
The Fuel Cell System Efficiency (Heating and Electrical) / 14.6:
The Effect of Different Temperatures on System Efficiency / 14.6.1:
The Fuel Utilization Factor and Efficiencies of the System / 14.6.2:
The System Efficiencies and Operating Pressure / 14.6.3:
Integrated New Clean Energy System / 14.7:
Index / 14.8:
Preface
Solid Oxide Fuel Cell with Ionic Conducting Electrolyte / Part I:
Introduction / Bin Zhu and Peter D. Lund1:
8.

図書

図書
SPE Technical Conference and Exhibition ; Society of Petroleum Engineers of AIME
出版情報: Richardson, Tex. : Society of Petroleum Engineers , Red Hook, NY : Printed from e-media with permission by Curran Associates, 2020, c2019  p. 737-1473 ; 28 cm
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9.

電子ブック

EB
Bernhaupt, Carmelo Ardito, Stefan Sauer
出版情報: SpringerLink Books - AutoHoldings , Springer International Publishing, 2020
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10.

電子ブック

EB
出版情報: IEEE Electronic Library (IEL) Standards , IEEE, 2020
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