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図書
herausgegeben von L. Zechmeister ... [et al.]
出版情報: Wien : Springer, 1938-  v. ; 24 cm
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The Dolastatins / Robert D. ; G.R. Pettit ; T. Nomura ; Shashi B. Mahato ; D.C. Gournelis ; H. Murray
The Naturally Occurring Coumarins: Scope of the Review / T. Fukai ; Saraswati Garai ; G.G. Laskaris ; A. CavF
Phenolic Constituents of Licorice (Glycyrrhiza Species): Triterpenoid Saponins
Triterpenoid Saponins
Progress in the Past Three Years / R. Verpoorte
Phenolic Compounds / B. FigadTre
Introduction
Introduction to Tables
Recent Methods of Structure Determination of Prenylated Phenols
Isolation
Cyclopeptide Alkaloids
Biological Activities of Phenolic Constituents of Glycyrrhiza Species / A. LaurensSchemes and Tables:
Structure Elucidation
Biological Activity / L.A. CollettScheme 1:
Variations of Ring-Attached Five-Carbon Units found in Coumarins
Production of Saponins by Tissue Culture / D. Cortes
Future Possibilities / M.T. Davies-ColemanScheme 2:
Variations of Five-Carbon Units Attached to Carbon and Oxygen in Coumarins
Acetogenins from Annonaceae
Reports of New Triterpenoid Saponins
Non-Oxygenated Coumarins / D.E.A. Rivett ; Leena A. OtsomaaTable 1:
Naturally Occurring 6-Substituted 5,6-Dihydro-Alpha-Pyrones
Oxygenated Coumarins / Ari M.P. KoskinenTables 2-7:
Synthesis of 6-Deoxyamino Sugars / Tables 8-16:
Dioxygenated Coumarins
Introduction; Known 6-Deoxyaminohexoses
Synthetic aspects / Tables 17-28:
Trioxygenated Coumarins
Tetraoxygenated Coumarins / Tables 29-34:
Biscoumarins / Table 35:
Triscoumarins / Table 36:
Structure Revision Required / Table 37:
Non-Macrocyclic Trichothecenes, Part 2 / J.F. Grove
Cardiac GlycosidesD. Deepak / S. Srivastava ; N.K. Khare ; A. Khare
Aspects of the Enzymology of the Shikimate Pathway / E. Haslam
Naturally Occurring Isocyano/Isothiocyanato and Related Compounds / C. W. J. Chang
Monoterpene Indole Alkaloids from Blue-Green Algae
Marine Diterpenes from Sponges
Marine Sesquiterpenes from Sponges
Uncommon Marine Analogs
Other Terrestrial Compounds
Biogenesis and Biosynthesis
Discussion and Summary
Addendum
Acknowledgment
References
Sulfur-Containing Amides from Glycosmis Species (Rutaceae) / O. Hofer ; H. Greger
Isolation and Structure Elucidation
Methylthiopropenoic Acid Amides
Methylsulfinylpropenoic Acid Amides
Methylsulfonylpropenoic Acid Amides
Methylthiocarbonic Acid Amides
Synthesis of Biogenic Sulfur-Containing Amides
Biosynthesis
Chemotaxonomy
Appendix: Sulfur-Containing Bisamides from Aglaia Species (Meliaceae)
List of Contributors
Synthesis Pathways to Erythrina Alkaloids and Erythrina Type Compounds / E. Reimann
Structural Classification of Erythrina Alkaloids / 1:
New Erythrina Alkaloids / 3:
Biosynthesis of Erythrina Alkaloids / 4:
Erythrinane Alkaloids / 4.1:
Homoerythrinane Alkaloids / 4.2:
Syntheses of Erythrina Alkaloids and Erythrina Type Compounds / 5:
Methodical Classification / 5.1:
Erythrinanes / 5.2:
Final Formation of One Ring / 5.2.1:
Ring C (Route C) / 5.2.1.1:
Cyclization of N-Phenethylhydroindole Derivatives (Route C(a)) / 5.2.1.1.1:
Cyclization of Angulary Arylated Hydroindole Derivatives (Route C(b)) / 5.2.1.1.2:
Formation of Ring B (Route B) / 5.2.1.2:
Cyclization of N-substituted C5-Spiroisoquinoline Derivatives (Route B(a)) / 5.2.1.2.1:
Cyclization of C6-Substituted C5-Spiroisoquinoline Derivatives (Route B(b)) / 5.2.1.2.2:
Formation of Ring A (Route A) / 5.2.1.3:
Cycloaddition to Pyrroloisoquinolines (Route A(a)) / 5.2.1.3.1:
Intramolecular Aldol Condensation of Angularly Substituted Pyrroloisoquinoline (Route A(b)) / 5.2.1.3.2:
Simultaneous Formation of More Than One Ring / 5.2.2:
Simultaneous Formation of Rings B and C (Route B/C) / 5.2.2.1:
Cyclization of Secondary Diphenethyl- or (Cycloalkyl)ethyl-phenethylamine Derivatives(Route B/C(a)) / 5.2.2.1.1:
Cyclization of Tertiary Cyclohexyl-ethyl-phenethyl-amide Derivatives (Route B/C(b)) / 5.2.2.1.2:
Cyclization of N-Substituted 1-Acyldihydroisoquinolinium Derivatives (Route A/B) / 5.2.2.2:
Cyclization of a Highly Functionalized Homoveratrylimide (Route A/B/C) / 5.2.2.3:
Homoerythrinanes / 5.3:
Biomimetic Routes / 5.3.1:
Final C Ring Formation Starting from N-Substituted Phenylhydroindoles / 5.3.2:
A Ring Formation by [2 + 2] Photocycloaddition to Pyrrolobenzazepines / 5.3.3:
Simultaneous B Ring Formation/C Ring Expansion Starting from Spiro-2-tetralones / 5.3.4:
Pharmacology / 6:
Concluding Remarks / 7:
The Trichothecenes and Their Biosynthesis / J. F. Grove (f)
The Trichothecenes
Macrocyclic and Non-Macrocyclic Compounds / 2.1:
Trichothecene Relatives / 2.2:
Sources / 2.3:
Oxygenation Pattern / 2.4:
Simple Trichothecenes / 3.1:
Mevalonic Acid to Trichodiene / 3.1.1:
Trichodiene to 12,13-Epoxytrichothecene and Isotrichodermol / 3.1.2:
Further Oxygenation and Esterification of the Trichothecene Nucleus: Biosynthesis of Specific Metabolites / 3.1.3:
Trichothecolone / 3.1.3.1:
Vomitoxin and Derivatives / 3.1.3.2:
T-2 Toxin / 3.1.3.3:
Nivalenol and Derivatives / 3.1.3.4:
Trichothecene Biosynthetic Gene Clusters / 3.1.4:
Trichoverroids and Macrocyclic Trichothecenes / 3.2:
Melanin, Melanogenesis, and Vitiligo / S. Roy3.3:
Melanin
Chemistry of Melanin / 1.1:
Isolation and Analysis
Solubilization
Protein Content
Carboxylic and Phenolic Function
Chemical Degradation / 2.5:
Reductive Methods / 2.5.1:
Oxidative Methods / 2.5.2:
Pyrolytic Methods / 2.5.3:
Spectroscopic Studies / 2.6:
UV and IR Spectroscopy / 2.6.1:
NMR Spectroscopy / 2.6.2:
X-Ray Defraction Study / 2.6.3:
ESR Study / 2.6.4:
Structure of Melanin / 2.7:
Melanin as Homopolymer / 2.7.1:
Melanin as Poikilopolymer / 2.7.2:
Melanin as Bipolymer / 2.7.3:
Biophysical Model of Melanin Structure / 2.7.4:
Structure of Phaeomelanin / 2.7.5:
Synthesis of Melanin / 2.8:
Electrochemical Synthesis / 2.8.1:
Photochemical Synthesis / 2.8.2:
Characteristic Biophysicochemical Properties of Melanin
Interaction of Melanin with Light
Melanin in UV and Visible Light
Melanin in the Photoprotection of Skin
Melanin as Light Screen in Eyes
Melanin and Its Redox Function
Binding Complexation and Medicinal Aspects of Melanin
Use of Melanin for Defence / 3.4:
Melanogenesis
Melanogenesis in vivo
Melanocytes / 4.1.1:
The Characteristics of the Enzyme / 4.1.2:
Regulation of Melanogenesis / 4.1.3:
Physiological Factors / 4.1.3.1:
Organic Sulfur Compounds / 4.1.3.2:
Metal Ions and Other Chemicals / 4.1.3.3:
Vitamins / 4.1.3.4:
Hormones / 4.1.3.5:
Neural Influence / 4.1.3.6:
Malpighian Cells / 4.1.3.7:
UV Light / 4.1.3.8:
Melanogenesis in vitro
Enzymatic Melanin Synthesis / 4.2.1:
Rearrangement of Dopachrome / 4.2.1.1:
Polymerization of DHI / 4.2.1.2:
Non-Enzymatic Melanin Synthesis: Model Reaction / 4.2.2:
Udenfriend System: A Model for Mixed Function Oxidase / 4.2.2.1:
Melanin Formation Under Udenfriend Conditions / 4.2.2.2:
Vitiligo
Melanocytotoxicity: Antimelanocyte-Antibodies Formation
The Immune Hypothesis
The Neural Hypothesis
The Self-Destruction Hypothesis / 5.2.3:
The Composite Hypothesis / 5.2.4:
Chemotherapy of Vitiligo
Psoralens
Psoralen Action and UV Light
Psoralen Action on Melanogenesis
Abnormal Biochemical Parameters in Vitiligo / 5.4:
Status of Tryptophan in the Melanogenic System / 5.5:
A Composite Hypothesis on Vitiligo / 5.6:
Author Index
Subject Index
List of Contributor
Pyrroles from Vertebrates / 1.:
Pyrroles from Invertebrates / 3.:
Pyrroles from Insects / 3.1.:
Pyrroles from Ants / 3.1.1.:
Pyrroles from Beetles / 3.1.2.:
Pyrrole Pheromones from Butterflies / 3.1.3.:
Pyrroles from Sponges / 3.2.:
Pyrrole-2-Carboxylates from Sponges / 3.2.1.:
Pyrrole-2-Carboxamides from Sponges / 3.2.2.:
Pyrrole-2-Carboxamides of the Oroidin Type / 3.2.2.1.:
Cyclized Oroidin Metabolites / 3.2.2.2.:
Dimeric Oroidin Metabolites / 3.2.2.3.:
Alkyl Pyrroles from Sponges / 3.2.3.:
Aryl Pyrroles from Sponges / 3.2.4.:
Hydroxy Pyrroles from Sponges / 3.2.5.:
Tetramic Acid Derivatives from Sponges / 3.2.6.:
Pyrroles from Other Invertebrates / 3.3.:
Aryl Pyrroles / 3.3.1.:
Other Pyrrole Derivatives / 3.3.2.:
Pyrroles from Protozoa / 3.4.:
Pyrroles from Plants / 4.:
Dihydropyrrolizine Derivatives / 4.1.:
Pyrrole-2-Carboxylic Acid Derivatives from Plants / 4.2.:
Pyrrolinone Derivatives in Plants / 4.3.:
Pyrroles from Fungi / 5.:
Pyrroles from Basidiomycetes / 5.1.:
Pyrroles from Deuteromycetes / 5.2.:
Pyrroles from Myxomycetes / 5.3.:
Pyrrolinone Derivatives in Fungi / 5.4.:
Tetramic Acid Derivatives in Fungi / 5.5.:
Pyrroles from Bacteria / 6.:
Halogenated Monopyrroles from Bacteria / 6.1.:
Halogenated Benzylpyrroles / 6.1.1.:
Halogenated Benzoylpyrroles / 6.1.2.:
Halogenated [alpha]-Arylpyrroles / 6.1.3.:
Halogenated [beta]-Arylpyrroles / 6.1.4.:
Pyrrole-2-carboxylates from Bacteria / 6.2.:
Pyrrole-2-carboxamides from Bacteria / 6.3.:
The Distamycin Group / 6.3.1.:
Pyrrol-2-carbacyl Derivatives from Bacteria / 6.4.:
[alpha]-Pyridylpyrroles from Bacteria / 6.5.:
Other Monopyrrole Derivatives from Bacteria / 6.6.:
Prodigiosins / 6.7.:
Prodigiosins from Eubacteria / 6.7.1.:
Prodiginines from Actinomycetes / 6.7.2.:
Hydroxy Pyrroles from Bacteria / 6.8.:
Tetramic Acid Derivatives from Prokaryotes / 6.9.:
Derivatives of 3-Acetyltetramic Acid from Actinomycetes / 6.10.:
Synthetic Aspects of Iridoid Chemistry / H. Franzyk
Classification of Iridoids
Availability and Production of Iridoids
Semi-Synthetic Conversions Between Iridoids
Monoterpene Alkaloids Structurally Related to Iridoids
Syntheses from Iridoids; References
The Defensive Chemistry of Ants / S. Leclercq ; J. C. Braekman ; D. Daloze ; J. M. Pasteels
Introduction; Alkaloids
Nonalkaloidal Compounds
Naturally Occurring Plant Coumarins / R.D.H. Murray
Artemisinin: An Endoperoxidic Antimalarial from Artemisia annua L / H. Ziffer ; R.J. Highet ; D.L. Klayman
Marine Glycolipids / E. Fattorusso ; A. Mangoni
Brassinosteroids / G. Adam ; J. Schmidt ; B. Schneider
Natural Occurrence and Distribution
Structures
Isolation and Purification
Analysis of Brassinosteroids
Synthesis; Biosynthesis
Metabolism of Brassinosteroids
Physiological Action
Molecular Mode of Action
Conclusions
Chemistry of the Neem Tree (//Azadirachta indica//A. Juss.) / A. Akhila ; K. Rani
Introduction; Chemistry of Limonoids; C-Seco Meliacins; Other Compounds
Secondary Metabolites and the Control of Some Blue Stain and Decay Fungi / W. A. Ayer ; L. S. Trifonov
Introduction; Blue Stain Fungi
Decay Causing Fungi
The Black Gall Effect
Condensed Tannins / D. Ferreira ; E. V. Brandt ; J. Coetzee ; E. Malan
Introduction; Formation of the Interflavanyl Bond in Oligomeric Proanthocyanidins
Cleavage of the Interflavanyl Bond in Oligomeric Proanthocyanidins
Rearrangement of the Pyran Heterocycle of Oligomeric Proanthocyanidins
Conformational Analysis of Dimeric Proanthocyanidins
Conclusion
Constituents of //Lactarius// (Mushrooms) / W. M. Daniewski ; G. Vidari
Introduction; Sesquiterpenes Isolated from //Lactarius//; Introduction to Parts 6 and 7 - Velutinal Esters and Related Sesquiterpenes
Chemistry of Sesquiterpenes of //Lactarius//
Nitric Oxide: Physiological Roles, Biosynthesis and Medical Uses / D. R. Adams ; M. Brochwicz-Lewinski ; A. R. Butler
Discovery in the Vasculature
Platelet Aggregation
NO and the Immune System
NO and the Nervous System
S-Nitrosothiols
NO Activity in the Mammalian Eye
The NO Biosynthetic Pathway
Mechanism of the Nitric Oxide Synthase-Catalysed Reaction
Nitric Oxide Synthase Structure
Clinical Uses of NO and Its Inhibitors
Acknowledgements
Microbial Siderophores / Herbert Budzikiewicz
Peptide Siderophores
Pyoverdins and Related Siderophores from Pseudomonas Spp
Azomonas and Azotobacter Siderophores
Anachelin
Actinomycetal Metabolites
Bacterial Hydroxamate Siderophores
Fungal L-Ornithine-Based Hydroxamate Siderophores
Catecholate Siderophores
Lipopeptidic Siderophores
Pseudomonas mendocina Siderophores / 2.9:
Siderophores Based on Diamino- and Triaminoalkane Skeletons
Rhizobactin
Hydroxamic Acid Siderophores
Citrate Siderophores
Siderophores with Two Hydroxamic Acid Units
Siderophores with 2-Oxoglutaric Acid Units
Siderophores with Two Catecholate Units / 4.3:
Siderophores with Two Citric Acid Units / 4.4:
Legiobactin / 4.5:
Pyochelin and Related Structures
Miscellaneous Siderophores
Selected Syntheses / 8:
Anachelin H / 8.1:
Alterobactin / 8.2:
Parabactin / 8.3:
Nannochelin A / 8.4:
Pyochelin / 8.5:
Epilog / 9:
Appendix
Notes Added in Proof
Resin Glycosides from the Morning Glory Family / Rogelio Pereda-Miranda ; Daniel Rosas-Ramírez ; Jhon Castañeda-Gómez
Ethnobotanical Background and Discovery
Structural Diversity
Chemical Composition
Resin Glycosides
Isolation Techniques
Structure Elucidation of Resin Glycosides
Degradative Chemical Methods
Spectroscopic Methods
Crystallographic Methods
Molecular Modeling
Strategies for Synthesis
Tricolorin A / 6.1:
Ipomoeassin E / 6.2:
Woodrosin I / 6.3:
Significance
Traditional Medicine and Morning Glories / 7.1:
Biological Activities / 7.2:
Pharmacology and Toxicology / 7.3:
Chemical Ecology / 7.4:
Chlorophyll Catabolites / B. Krautler
Chlorophyll Catabolites from Vascular Plants
Green Chlorophyll Degradation Products in Vascular Plants
Chlorophyllide a and b from Chlorophylls by Loss of the Phytol Side Chain / 2.1.1:
Reductive Path from b- to a-Type Chlorophyll(ide)s / 2.1.2:
Pheophorbide a from Chlorophyllide a by Removal of the Magnesium Ion / 2.1.3:
13[superscript 2]-Carboxy-pyropheophorbide a from Hydrolysis and Pyropheophorbide a from Overall Loss of the Methoxycarbonyl Group from Pheophorbide a / 2.1.4:
Non-green Chlorophyll Degradation Products from Vascular Plants
Discovery and Structure Analysis of Fluorescent Chlorophyll Catabolites / 2.2.1:
Preparation of the Elusive Red Chlorophyll Catabolite by Partial Synthesis / 2.2.2:
An Enzyme-bound Red Chlorophyll Catabolite from Enzymatic Oxygenation of Pheophorbide a / 2.2.3:
Fluorescent Chlorophyll Catabolites from Enzymatic Reduction of the Red Chlorophyll Catabolite / 2.2.4:
Model Experiments for the Reduction of the Red Chlorophyll Catabolite to Fluorescent Chlorophyll Catabolites / 2.2.5:
Non-fluorescent Colourless Chlorophyll Catabolites / 2.2.6:
A Non-enzymatic Tautomerization Achieves the "Final" Transformation of Fluorescent Chlorophyll Catabolites to Non-fluorescent Colourless Chlorophyll Catabolites / 2.2.7:
Peripheral Functional Groups and Conjugations Found in Non-fluorescent Colourless Chlorophyll Catabolites / 2.2.8:
Evidence for Further Breakdown of the Non-fluorescent Colourless Chlorophyll Catabolites in Higher Plants / 2.2.9:
Chlorophyll Catabolites from the Green Alga Chlorella protothecoides
Chlorophyll Catabolites from Marine Organisms
Conclusions and Outlook
Steroidal Saponins / N. P. Sahu ; S. Banerjee ; N. B. Mondal ; D. Mandal
Conventional Methods
Spectrometry Coupled with Chemical Methods
Modern Spectrometric Methods
Mass Spectrometry / 3.3.1:
[superscript 1]H NMR Spectroscopy / 3.3.2:
[superscript 13]C NMR Spectroscopy / 3.3.2.2:
2D NMR Spectroscopy / 3.3.2.3:
Cytotoxic Activity Against Cancer Cell Lines
Antifungal Activity
Miscellaneous Effects
Biosynthesis of Steroidal Glycosides
Report of New Steroidal Saponins (1998-Mid-2006)
Acknowledgement
Non-conventional Lignans: Coumarinolignans, Flavonolignans, and Stilbenolignans / Sajeli A. Begum ; Mahendra Sahai ; Anil B. Ray
Coumarinolignans
Occurrence of Coumarinolignans
Classification of Coumarinolignans
Structure Elucidation of Coumarinolignans
Chemistry of Coumarinolignans
Biological Activity of Coumarinolignans
Biogenesis of Coumarinolignans
Flavonolignans
Occurrence of Flavonolignans
Features of Flavonolignans and Their Classification
Structure Elucidation of Flavonolignans
Chemistry of Flavonolignans
Biological Activity of Flavonolignans / 3.5:
Biogenesis of Flavonolignans / 3.6:
Stilbenolignans
Occurrence and Features of Stilbenolignans
Structure Elucidation and Synthesis of Stilbenolignans
Biological Activity of Stilbenolignans
Biogenesis of Stilbenolignans
Picrotoxanes / Edda Gössinger
Tabular Overview of the Picrotoxanes
Occurrence
Systematic and Geographic Occurrence of Picrotoxane-Containing Plants
Parasitic Plants
Picrotoxanes Found in Animals and Animal Products
The Riddle of the Scattered Taxonomic Occurrence of Picrotoxanes
Isolation of Picrotoxanes
Examples of Recent Isolation Procedures
Structure Determination of Picrotoxanes
Main Picrotoxanes of the Menispermaceae
Main Picrotoxanes of the Coriariaceae
Picrotoxanes Isolated from Toxic Honey
Picrotoxanes of the Picrodendraceae
Picrotoxanes from Dendrobium Species
Total Syntheses of Picrotoxanes
Overview
Description of the Syntheses
Biosynthesis of Picrotoxanes
Investigations on the Biosynthesis of Dendrobines
Investigations on the Biosynthesis of Sesquiterpene Picrotoxanes
Physiological Activity of Picrotoxanes
Toxicity
Picrotoxanes as Therapeutics
Picrotoxanes as Epileptogenic Compounds
Picrotoxanes as Tools in Neurobiological Research
Abbreviations
Combinatorial and Synthetic Biosynthesis in Actinomycetes / Marta Luzhetska ; Johannes Härle ; Andreas Bechthold
Combinatorial Biosynthesis and Synthetic Biosynthesis
Achievements in Combinatorial Biosynthesis
Challenges for Combinatorial Biosynthesis
Synthetic Biosynthesis
The Dolastatins / Robert D. ; G.R. Pettit ; T. Nomura ; Shashi B. Mahato ; D.C. Gournelis ; H. Murray
The Naturally Occurring Coumarins: Scope of the Review / T. Fukai ; Saraswati Garai ; G.G. Laskaris ; A. CavF
Phenolic Constituents of Licorice (Glycyrrhiza Species): Triterpenoid Saponins
2.

図書

東工大
目次DB

図書
東工大
目次DB
editors, T. Inui ... [et al.]
出版情報: Amsterdam ; Tokyo : Elsevier Science, c1998  xix, 699 p. ; 25 cm
シリーズ名: Studies in surface science and catalysis ; 114
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Preface
Organization
Sponsoring
Special Lecture
   International Energy Agency action on climate change issues M.A. Preville and H.J. Koch (France) 1
Plenary Lecture
   Japan's basic strategy concerning countermeasures to mitigate climate change T. Namiki (Japan) 9
   Research and development on new synthetic routes for basic chemicals by catalytic hydrogenation of CO2 H. Arakawa (Japan) 19
   New approaches in CO2 reduction A. Fujishima, D.A. Tryk and T.N. Rao (Japan) 31
   Development of electrocatalysts for carbon dioxide reduction using polydentate ligands to probe structure-activity relationships D.L. DuBois (USA) 43
   Carbon dioxide and microalgae N. Kurano, T. Sasaki and S. Miyachi (Japan) 55
   Perspectives of carbon dioxide utilization in the synthesis of chemicals. coupling chemistry with biotechnology. M. Aresta (Italy) 65
Keynote Lecture
   Scope of studies on CO2 mitigation K. Yamada (Japan) 77
   Hydrogenation of CO2 toward methanol Influence of the catalysts composition and preparation on the catalytic behavior R. Kieffer and L. Udron (France) 87
   Photochemical carbon dioxide reduction with metal complexes: Differences between cobalt and nickel macrocycles E. Fujita, B.S. Brunschwig, D. Cabelli, M.W. Renner, L.R. Furenlid, T. Ogata, Y. Wada and S. Yanagida (USA) 97
   Electrochemical reduction of CO2 at metallic electrodes J. Augustynski, P. Kedzierzawski and B. Jermann (Switzerland) 107
   Super-RuBisCO: Improvement of photosynthetic performances of plants A. Yokota (Japan) 117
   Organometallic reactions with CO2 - Catalyst design and mechanisms E. Dinjus (Germany) 127
Oral Presentation
   Catalytic fixation of CO2: CO2 purity and H2 supply J.N. Armor (USA) 141
   Reduction of carbon dioxide to graphite carbon via methane by catalytic fixation with membrane reactor H. Nishiguchi, A. Fukunaga, Y. Miyashita, T. Ishihara and Y. Takita (Japan) 147
   Catalytic reaction of CO2 with C2H4 on supported Pt-Sn bimetallic catalysts J. Llorca, P. Ramirez de la Piscina, J. Sales and H. Homs (Spain) 153
   Initial transient rates and selectivities of Fischer-Tropsch synthesis with CO2 as carbon source H. Schulz, G. Schaub, M. Claeys, T. Riedel and S. Walter (Germany) 159
   Palladium-catalyzed carboxylation of allyl stannanes and carboylative coupling of allyl stannanes and allyl halides M. Shi, R. Franks and K.N. Nicholas (USA) 165
   Interaction between CO2 and propylene on Ru-Co/Al2O3-catalysts of cluster type G.D. Zakumbaeva, L.B. Shapovalova and I.A. Shlygina (Kazakhstan) 171
   Photocatalytic reduction of CO2 with H2O on titanium oxides anchored within zeolites M. Anpo, H. Yamashita, K. Ikeue, Y. Fujii, Y. Ichihashi (Japan), S.G. Zhang, D.R. Park (Korea), S. Ehara (Japan), S.-E. Park, J.-S. Chang and J.W. Yoo (Korea) 177
   Photocatalytic reduction and fixation of CO2 on cadmium sulfide nanocrystallites S. Yanagida, Y. Wada, K. Murakoshi, H. Fujiwara, T. Sakata and H. Mori (Japan) 183
   Abiotic photosynthesis of amino acids, nucleic acid bases and organic acids from CO2 dissolved in aqueous solution S. Kihara, K. Maeda, T. Hori and T. Fujinaga (Japan) 189
   Aspects of CO2 utilization toward the goal of emission reduction in Romania L. Dragos, N. Scarlat, M. Neacsu and C. Flueraru (Romania) 195
   CO2 capture and utilization for enhanced oil recovery (EOR) and underground storage A case study in JiLin Oil Field, China G. Yun, D. Liu, T. Wu, J. Wu, X. Ji and Z. Li (China) 201
   Electrocatalytic reduction of CO2 to worthier compounds on a functional dual-film electrode with a solar cell as the energy source K. Ogura, M. Yamada, M. Nakayama and N. Endo (Japan) 207
   Incorporation of CO2 into organic perfluoroalkyl derivatives by electrochemical methods E. Chiozza, M. Desigaud, J. Greiner and E. Dunach (France) 213
   Molecular tailoring of organometallic polymers for efficient catalytic CO2 reduction: mode of formation of the active species R. Ziessel (France) 219
   Electroreduction of CO2 using Cu/Zn oxides loaded gas diffusion electrodes S. Ikeda, S. Shiozaki, J. Susuki, K. Ito and H. Noda (Japan) 225
   Recent slow rate of CO2 increase and vegetation activity K. Kawahira and Y. Maeda (Japan) 231
   Production of PHA (poly hydroxyalkanoate) by genetically engineered marine cyanobacterium H. Miyasaka, H. Nakano, H. Akiyama, S. Kanai and M. Hirano (Japan) 237
   Cellulose as a biological sink of CO2 T. Hayashi, Y. Ihara, T. Nakai, T. Takeda and R. Tominaga (Japan) 243
   Possibility of molecular protection of photosynthesis under salinity stress F. Sato, Y. Arata, K. Matsuguma, M. Shiga, Y. Kanda, K. Ifuku, K. Ishikawa and T. Yoshida (Japan) 249
   Organometallic CO2 complexes in supercritical CO2: a time-resolved infrared study M.W. George, D.C. Grills, X-Z. Sun and M. Poliakoff (UK) 255
   Methanation of carbon dioxide on catalysts derived from amorphous Ni-Zr-rare earth element alloys H. Habazaki, T. Yoshida, M. Yamasaki, M. Komori, K. Shimamura, E. Akiyama, A. Kawashima and K. Hashimoto (Japan) 261
   Development of high performance Raney copper-based catalysts for methanol synthesis from CO2 and H2 J. Toyir, M. Saito, I. Yamauchi, S. Luo, J. Wu, I. Takahara and M. Takeuchi (Japan) 267
   Global carbon-recycling energy delivery system for CO2 mitigation (I) Carbon one-time recycle system towards carbon multi-recycle system H. Sano, Y. Tamaura, H. Amano and M. Tsuji (Japan) 273
   Oil extraction by highly pressurized CO2 produced in zero emission power plants Ph. Mathieu, E. Iantovski and V. Kushnirov (Belgium) 279
   Global carbon-recycling energy delivery system for CO2 mitigation (III) Fossil/solar energy hybridization system for utilization of Carbon as solar energy carrier Y. Tamaura, M. Tsuji, H. Amano and H. Sano (Japan) 285
   Review of measures to mitigate carbon dioxide emissions in the Slovak Republic and modes of utilization A. Moncmanova (Slovak Republic) 291
   Proposal of a new high-efficient gas turbine power generation system utilizing waste heat from factories P.S. Pak, H. Ueda and Y. Suzuki (Japan) 297
   Acetogenesis and the primary structure of the NADP-dependent formate dehydrogenase of Clostridium thermoaceticum, a tungsten-selenium-iron protein D.J. Gollin, X.-L. Li, S.-M. Liu and L.G. Ljungdahl (USA) 303
   Biochemical CO2 fixation by mimicking zinc (II) complex for active site of carbonic anhydrase K. Ichikawa, K. Nakata, M. Ibrahim and S. Kawabata (Japan) 309
   The biological CO2 fixation using Chlorella sp. with high capability in fixing CO2 M. Murakami, F. Yamada, T. Nishide, T. Muranaka, N. Yamaguchi and Y. Takimoto (Japan) 315
   Photobiological production of hydrogen gas Y. Asada (Japan) 321
   Hydrocarbon synthesis from CO2 over composite catalysts Y. Souma, M. Fujiwara, R. Kieffer, H. Ando and Q. Xu (Japan) 327
   CO2 for petrochemicals feedstock. Conversion to synthesis gas on metal supported catalysts. P. Gronchi, P. Centola and R. Del Rosso (Italy) 333
   Iron catalyzed CO2 hydrogenation to liquid hydrocarbons R.A. Fiato, E. Iglesia, G.W. Rice and S.L. Soled (USA) 339
   Support effects of the promoted and unpromoted iron catalysts in CO2 hydrogenation K.-W. Jun, S.-J. Lee, H. Kim, M.-J. Choi and K.-W. Lee (Korea) 345
   Methanol synthesis from CO2/H2 over Pd promoted Cu/ZnO/Al2O3 catalysts M. Sahibzada, I.S. Metcalfe and D. Chadwick (UK) 351
   A 50Kg/day class test plant for methanol synthesis from CO2 and H2 K. Ushikoshi, K. Mori, T. Watanabe, M. Takeuchi and M. Saito (Japan) 357
Poster Presentation
   Comparison of CO2 sources for the synthesis of renewable methanol M. Specht, A. Bandi, M. Elser and F. Staiss (Germany) 363
   Characteristics and economics assessment of power generation systems utilizing solar energy in various regions T. Kosugi, P.S. Pak and Y. Suzuki (Japan) 367
   Solar/chemical energy hybridization via Boudouard reaction H. Ono, M. Kawabe, M. Nezuka, M. Tsuji and Y. Tamaura (Japan) 371
   Development of active and stable nickel-magnesia solid solution catalysts for CO2 reforming of methane K. Tomishige, Y. Chen, X. Li, K. Yokoyama, Y. Sone, O. Yamazaki and K. Fujimoto (Japan) 375
   Global carbon-recycling energy delivery system for CO2 mitigation (II) Two possible ways for introducing solar energy M. Tsuji, H. Amano, Y. Tamaura, H. Sano and S. Maezawa (Japan) 379
   Efficient thermochemical cycle for CO2 reduction with coal using a reactive redox system of ferrite T. Kodama, A. Aoki, S. Miura and Y. Kitayama (Japan) 383
   Oxidative dehydrogenation of ethylbenzene with carbon dioxide over ZSM-5-supported iron oxide catalysts J.-S. Chang, S.-E. Park, W.Y. Kim (Korea) M. Anpo and H. Yamashita (Japan) 387
   Nature of CO2 adsorbed on MgO surface at low temperatures T. Ito, H. Isawa, H. Kishimoto, H. Kobayashi and K. Toi (Japan) 391
   CO2 behavior on supported KNiCa catalyst in the carbon dioxide reforming of methane S.-E. Park, J.-S. Chang, H.-S. Roh (Korea), M. Anpo and H. Yamashita (Japan) 395
   Utilization of CO2 in the reforming of natural gas on carbon supported ruthenium catalysts. Influence of MgO addition P. Ferreira-Aparicio, B. Bachiller-Baeza, A. Guerrero-Ruiz and I. Rodriguez-Ramos (Spain) 399
   Catalytic conversion of carbon dioxide to polymer blends via cyclic carbonates D.W. Park, J.Y. Moon, J.G. Yang, S.M. Jung, J.K. Lee and C.S Ha (Korea) 403
   The selective synthesis of lower olefins (C2-C4) by the CO2 hydrogenation over Iron catalysts promoted with Potassium and supported on ion exchanged (H,K) Zeolite-Y H. Kim, D.-H. Choi, S.-S. Nam, M.-J. Choi and K.-W. Lee (Korea) 407
   Hydrogenation of carbon dioxide over rhodium catalyst supported on silica M. Kishida, K. Onoue, S. Tashiro, H. Nagata and K. Wakabayashi (Japan) 411
   Dehydrogenation of ethylbenzene over iron oxide-based catalyst in the presence of carbon dioxide N. Mimura, I. Takahara, M. Saito, T. Hattori, K. Ohkuma and M. Ando (Japan) 415
   Promoting effects of CO2 on dehydrogenation of propane over a SiO2-supported Cr2O3 catalyst I. Takahara, W.-C. Chang, N. Mimura and M. Saito (Japan) 419
   Hydrogenation of carbon dioxide over Fe-Cu-Na/zeolite composite catalysts Q. Xu, D. He, M. Fujiwara, M. Tanaka, Y. Matsumura, Y. Souma, H. Ando and H. Yamanaka (Japan) 423
   Fe promoted Cu-based catalysts for hydrogenation of CO2 N. Nomura, T. Tagawa and S. Goto (Japan) 427
   The effect of rhodium precursor on ethanol synthesis by catalytic hydrogenation of carbon dioxide over silica supported rhodium catalysts H. Kusama, K. Okabe, K. Sayama and H. Arakawa (Japan) 431
   Selective formation of iso-butane from carbon dioxide and hydrogen over composite catalysts Y. Tan, M. Fujiwara, H. Ando, Q. Xu and Y. Souma (Japan) 435
   Vanadium-catalyzed acetic acid synthesis from methane and carbon dioxide Y. Taniguchi, T. Hayashida, T. Kitamura and Y. Fujiwara (Japan) 439
   Fuels and petrochemicals from CO2 via Fischer-Tropsch synthesis - steady state catalyst activity and selectivity T. Riedel, S. Walter, M. Claeys, H. Schulz and G. Schaub (Germany) 443
   Effective conversion of CO2 to methanol and dimethyl ether over hybrid catalysts K.-W. Jun, M.-H. Jung, K.S. Rama Rao, M.-J. Choi and K.-W. Lee (Korea) 447
   Characterization of CO2 methanation catalysts prepared from amorphous Ni-Zr and Ni-Zr-rare earth element alloys M. Yamasaki, H. Habazaki, T. Yoshida, M. Komori, K. Shimamura, E. Akiyama, A. Kawashima, K. Asami and K. Hashimoto (Japan) 451
   Hydrogenation of CO2 over Rh ion exchanged zeolite catalysts K.K. Bando, K. Soga, K. Kunimori, N. Ichikuni, K. Asakura, K. Okabe, H. Kusama, K. Sayama and H. Arakawa (Japan) 455
   Interconversion of Ru-Co and Ru-η1-CO2 through reversible oxide transfer reaction K. Tsuge, K. Tanaka and H. Nakajima (Japan) 459
   Physiological properties of phosphoenolpyruvate carboxylase and phosphoenolpyruvate carboxykinase from Rhodopseudomonas sp No. 7 T. Fujii, M. Sadaie, M. Saijou, T. Nagano, T. Suzuki, M. Ohtani and H. Shinoyama (Japan) 463
   Production of alkane and alkene from CO2 by a petroleum-degrading bacterium strain HD-1 M. Morikawa, T. Iwasa, K. Nagahisa, S. Yanagida and T. Imanaka (Japan) 467
   Cultivation of cyanobacterium in various types of photobioreactors for biological CO2 fixation I.S. Suh, C.B. Park, J.-K. Han and S.B. Lee (Korea) 471
   Application of photosynthetic bacteria for porphyrin production H. Yamagata, R. Matoba, T. Fujii and H. Yukawa (Japan) 475
   Utilization of micro-algae for building materials after CO2 fixation T. Otsuki, M. Yamashita, T. Hirotsu, H. Kabeya and R. Kitagawa (Japan) 479
   Photosynthetic CO2 fixation performance by a helical tubular photobioreactor incorporating Chlorella sp. under outdoor culture conditions Y. Watanabe, M. Morita and H. Saiki (Japan) 483
   Carboxylation reaction with carbon dioxide. Mechanistec studies on the Kolbe-Schmitt reaction. Y. Kosugi and K. Takahashi (Japan) 487
   From carbon dioxide to C2 organic molecules mediated by Aresta's nickel carbon dioxide complex J.K. Gong, C.A. Wright, M. Thorn, K. McCauley, J.W. McGill, A. Sutterer, S.M. Hinze and R.B. Prince (USA) 491
   Methanol homologation using carbon dioxide catalyzed by ruthenium-cobalt bimetallic complex system K. Tominaga, Y. Sasaki, T. Watanabe and M. Saito (Japan) 495
   Atmospheric CO2 fixation by dinuclear Ni(II) complex, [TRANi(II)(μ-OH)2Ni(II)TPA](ClO4)2 (TPA=Trist(pyridymethyl)amine) M. Ito, T. Ishihara and Y. Takita (Japan) 499
   Carbon dioxide fixation with lanthanoid complex S. Inoue, H. Sugimoto, N. Ishida and T. Shima (Japan) 503
   A study on methanol synthesis through CO2 hydrogenation over copper-based catalysts S.-K. Ihm, Y.-K. Park, J.-K. Jeon, K.-C. Park and D.-K. Lee (Korea) 505
   Mechanistic studies of methanol synthesis from CO2/H2 on Cu/ZnO/SiO2 catalyst D.-K. Lee, D.-S. Kim, C.M. Yoo, C.-S. Lee and I.-C. Cho (Korea) 509
   Highly effective synthesis of ethanol from CO2 on Fe, Cu-based novel catalysts T. Yamamoto and T. Inui (Japan) 513
   A study for the durability of catalysts in ethaol synthesis by hydrogenation of carbon dioxide K. Higuchi, Y. Haneda, K. Tabata, Y. Nakahara and M. Takagawa (Japan) 517
   Development of stable catalysts for liquid-phase methanol synthesis from CO2 and H2 H. Mabuse, T. Watanabe and M. Saito (Japan) 521
   Ethanol synthesis from carbon dioxide and hydrogen M. Takagawa, A. Okamoto, H. Fujimura, Y. Izawa and H. Arakawa (Japan) 525
   New preparation method of Cu/ZnO catalysts for methanol synthesis from carbon dioxide hydrogenation by mechanical alloying H. Fukui, M. Kobayashi, T. Yamaguchi, H. Kusama, K. Sayama, K. Okabe and H. Arakawa (Japan) 529
   Promoting effect of calcium addition to Pd/SiO2 catalysts in CO2 hydrogenation to methanol A. L. Bonivardi, D.L. Chiavassa and M.A. Baltanas (Argentina) 533
   Direct synthesis of gasoline from carbon dioxide via methanol as the intermediate H. Hara, T. Takeguchi and T. Inui (Japan) 537
   Comparison of CO2 hydrogenation in a catalytic reactor and in a dielecric-barrier discharge A. Bill, B. Eliasson, U. Kogelschatz and L.-M. Zhou (Switzerland) 541
   Methanol synthesis from carbon dioxide on CuO-ZnO-Al2O3 catalysts M. Hirano, T. Akano, T. Imai and K. Kuroda (Japan) 545
   Optimization of preparation conditions and improvement of stability of Cu/ZnO-based multicomponent catalysts for methanol synthesis from CO2 and H2 S. Luo, J. Wu, J. Toyir, M. Saito, M. Takeuchi and T. Watanabe (Japan) 549
   Effect of solvents on photocatalytic reduction of carbon dioxide using semiconductor photocatalysts T. Torimoto, B.-J. Liu and H. Yoneyama (Japan) 553
   Application of electrospray mass spectrometry and high performance liquid chromatography in the elucidation of photocatalytic CO2-fixation reactions H. Hori, J. Ishihara, M. Ishizuka, K. Koike, K. Takeuchi, T. Ibusuki and O. Ishitani (Japan) 557
   Photocatalytic reduction of CO2 with H2O on Ti/Si binary oxide catalysts prepared by the solgel method H. Yamashita, S. Kawasaki, M. Takeuchi, Y. Fujii, Y. Ichihashi, Y. Suzuki (Japan), S.-E. Park, J.-S. Chang, J.W. Yoo (Korea) and M. Anpo (Japan) 561
   Photoelectrochemical reduction of CO2 at a metal-particle modified p-Si electrode in nonaqueous solutions Y. Nakamura, R. Hinogami, S. Yae and Y. Nakato (Japan) 565
   Infrared spectroscopic study of CO2 and CO reduction at metal electrodes O. Koga, T. Matsuo, H. Yamazaki and Y. Hori (Japan) 569
   Influence of anions on the production efficiency in pulsed electroreduction of CO2 on metal and alloy electrodes R. Shiratsuchi, S. Ishimaru and G. Nogami (Japan) 573
   Electrochemical reduction of CO2 by using metal supported gas diffusion electrode under high pressure K. Hara, N. Sonoyama and T. Sakata (Japan) 577
   Electrochemical reduction of carbon dioxide at a platinum electrode in acetonitrile-water mixtures Y. Tomita and Y. Hori (Japan) 581
   Electrochemical reduction of CO2 in micropores T. Yamamoto, D.A. Tryk, K. Hashimoto, A. Fujishima and M. Okawa (Japan) 585
   Photoelectrochemical reduction of highly concentrated CO2 in methanol solution K. Hirota, D.A. Tryk, K. Hashimoto, M. Okawa and A. Fujishima (Japan) 589
   Studies on CO2 fixation in PNSB: Utilization of waste as the additional source of carbon for CO2 fixation by PNSB V. Brenner, M. Inui, N. Nonoura, K. Momma and H. Yukawa (Japan) 593
   Studies on CO2 fixation in PNSB: Analysis of CO2 metabolism in purple non-sulfur bacteria M. Inui, J.H. Roh, K. Momma and H. Yukawa (Japan) 597
   Crystallization and preliminary X-ray studies of phosphoenolpyruvate carboxylase from Escherichia Coli H. Matsumura, T. Nagata, T. Inoue, Y. Nagara, T. Yoshinaga, K. Izui and Y. Kai (Japan) 601
   Molecular characterization of recombinant phosphoenolpyruvate carboxylase from an extreme thermophile T. Nakamura and K. Izui (Japan) 605
   Revertant of no-active RuBisCo tobacco mutant, Sp25, obtained by chloroplast transformation method using microprojectile bombardment K. Tomizawa, T. Shikanai, A. Shimoide, C.H. Foyer and A. Yokota (Japan) 609
   Reductive TCA cycle in an aerobic bacterium Hydrogenobacter thermophilus strain TK-6 M. Ishii, K. Yoon, Y. Ueda, T. Ochiai, N. Yun, S. Takishita, T. Kodama and Y. Igarashi (Japan) 613
   Carbon dioxide fixation and biomass production with blue-green algae Spirulina platensis S. Hirata and M. Hayashitani (Japan) 617
   Chitosan-calcium carbonate composites: Biomimetic mineralization of aqueous carbonate ions into chitosan-calcium alginate hydrogels S. Hirano, K. Yamamoto, H. Inui, K.I. Draget, K.M. Varum and O. Smidsrod (Japan) 621
   Tolerance of a green alga, Scenedesmus komarekii, to environmental extremes N. Hanagata, R. Matsukawa, M. Chihara and I. Karube (Japan) 625
   Over-expressed effect of carbonic anhydrase on CO2 fixation in cyanobacterium, Synechococcus sp. PCC7942 M. Murakami, N. Yamaguchi, T. Nishide, T. Muranaka and Y. Takimoto (Japan) 629
   CO2 removal by a bioreactor with photosynthetic algae using solar-collecting and light-diffusing optical devices M. Nanba and M. Kawata (Japan) 633
   Isolation and characterization of a green alga Neochloris sp. for CO2 fixation M. Kawata, M. Nanba, R. Matsukawa, M. Chihara and I. Karube (Japan) 637
   Antioxidant activity of CO2 fixing microalgae R. Matsukawa, Y. Wada, N. Tan, N. Sakai, M. Chihara and I. Karube (Japan) 641
   Screening of polysaccharide-producing microalgae Y. Shishido, M. Kawata, R. Matsukawa, M. Chihara and I. Karube (Japan) 645
   A marine microalga utilization for a paper: Semi-batch cultivation of Tetraselmis sp. Tt-1 by a tubular bioreactor and the partial substitution of whole kenaf pulp for a paper Y. Samejima, A. Hirano, K. Hon-Nami, S. Kunito, K. Masuda, M. Hasuike, Y. Tsuyu and Y. Ogushi (Japan) 649
   Conversion of CO2 into cellulose by gene manipulation of microalgae: Cloning of cellulose synthase genes from Acetobacter xylinum Y. Umeda, A. Hirano, K. Hon-Nami, S. Kunito, H. Akiyama, T. Onizuka, M. Ikeuchi and Y. Inoue (Japan) 653
   Ethanol production from carbon dioxide by fermentative microalgae S. Hirayama, R. Ueda, Y. Ogushi, A. Hirano, Y. Samejima, K. Hon-Nami and S. Kunito (Japan) 657
   Production of polyethylene glycol and polyoxyalkylenealkylphenyl ether microspheres using supercritical carbon dioxide K. Mishima, K. Matsuyama, Y. Taruta, M. Ezawa, Y. Ito and M. Nagatani (Japan) 661
   Carbon dioxide separation from nitrogen using Y-type zeolite membranes S. Morooka, T. Kuroda and K. Kusakabe (Japan) 665
   Comparative Study of various amines for the reversible absorption capacity of carbon dioxide Y. Nagao, A. Hayakawa, H. Suzuki, S. Mitsuoka, T. Iwaki, T. Mimura and T. Suda (Japan) 669
   Kinetic analysis of CO2 recovery from flue gas by an ecotechnological system M. Tabata, T. Chohji and E. Hirai (Japan) 673
   Formation of peroxocarbonates from L3Rh(O2)Cl and L2Ni(CO2): a unique reaction mechanism with carbon dioxide insertion into the O-O bond M. Aresta, E. Quaranta, I. Tommasi, J. Mascetti, M. Tranquille and M. Borowiak (Italy) 677
Keyword Index 681
Author Index 687
Preface
Organization
Sponsoring
3.

図書

図書
edited by S. Yoshida, ... [et al.]
出版情報: Zuerich, Switzerland : Trans Tech Publications, c2002  2 v. (xxxvii, 1562 p.) ; 25 cm
シリーズ名: Materials science forum ; v. 389-393
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4.

図書

図書
edited by Mino Green
出版情報: New York : M. Dekker, 1969-1973  3 v. ; 24 cm
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5.

図書

図書
edited by D.S. Chemla, J. Zyss
出版情報: Orlando ; Tokyo : Academic Press, 1987  2 v. ; 24 cm
シリーズ名: Quantum electronics : principles and applications
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6.

図書

図書
B.K. Vainshtein, V.M. Fridkin, V.L. Indenbom
出版情報: Berlin ; New York : Springer-Verlag, 1982  xvii, 433 p. ; 24 cm
シリーズ名: Springer series in solid-state sciences ; 21 . Modern crystallography ; 2
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7.

図書

図書
editors, J.-M. Richard, E. Aslanides, and N. Boccara
出版情報: Berlin ; Tokyo : Springer-Verlag, c1988  xii, 467 p. ; 25 cm
シリーズ名: Springer proceedings in physics ; v. 26
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8.

図書

図書
edited by Donald O. Thompson and Dale E. Chimenti
出版情報: New York : Plenum Press, c1982-  v. ; 26 cm
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目次情報: 続きを見る
Minisymposium
Development of Standard Techniques: Elastic Wave Scattering
Elastic Wave Propagation
Eddy Currents
Radiography and CT
Optical Techniques
Thermal Techniques
Emerging Inspection Technologies: LaserBased Ultrasonics
Interpretive Signal Processing and Image Analysis: Signal Processing
Neural Networks
Electromagnetic Techniques
Magnetic Resonance Methods
Imaging and Inversion Methods
Sensors and New Techniques: Ultrasonic and Acoustic Sensors
Electromagnetic Sensors
New Techniques and Simulations
Engineered Materials: Composite Properties
Composite Defects
Interfaces
Bonded Joints
Material Properties: Metals
Ceramics and Semiconductors
Microstructure and Surface Roughness
Magnetic Methods and Materials
Thin Films and Coatings
Corrosion
Nonlinearity, Deformation, and Fracture: Nonlinear Effects
Stress and Fatigue Cracks
Civil Structures and Materials
Systems, Process Control, and Reliability
317 articles
Index
Minisymposium
Development of Standard Techniques: Elastic Wave Scattering
Elastic Wave Propagation
9.

図書

図書
E.D. Goldberg, editor ; rapporteurs: M.O. Andreae ... [et al.] ; program advisory committee: E.D. Goldberg ... [et al.]
出版情報: Berlin : Springer-Verlag, 1982  384 p. ; 21 cm
シリーズ名: Dahlem workshop reports ; . Physical and chemical sciences research report ; 4
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10.

図書

図書
O. Madelung ; translated by B.C. Taylor
出版情報: Berlin ; New York : Springer-Verlag, 1978  xi, 488 p. ; 24 cm
シリーズ名: Springer series in solid-state sciences ; v. 2
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