Industrial dyes [[electronic resource] ] : chemistry, properties, applications / / Klaus Hunger (editor) |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2003 |
Descrizione fisica | 1 online resource (686 p.) |
Disciplina |
667.2
667.25 |
Altri autori (Persone) | HungerKlaus |
Soggetto topico |
Dyes and dyeing - Chemistry
Dyes and dyeing - Industrial applications |
Soggetto genere / forma | Electronic books. |
ISBN |
3-527-60606-8
9786612118388 1-282-11838-2 1-280-56073-8 9786610560738 3-527-60201-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Industrial Dyes Chemistry, Properties, Applications; Contents; Preface; List of Contributors; 1 Dyes, General Survey; 1.1 Introduction; 1.2 Classification Systems for Dyes; 1.3 Classification of Dyes by Use or Application Method; 1.4 Nomenclature of Dyes; 1.5 Equipment and Manufacture; 1.6 Economic Aspects; 1.7 References; 2 Important Chemical Chromophores of Dye Classes; Introduction; 2.1 Azo Chromophore; 2.1.1 Introduction; 2.1.2 General Synthesis; 2.1.2.1 Diazo Components; 2.1.2.2 Diazotization Methods; 2.1.2.3 Coupling Components; 2.1.2.4 Azo Coupling in Practice
2.1.3 Principal Properties2.1.3.1 Tautomerism; 2.1.3.2 Metallized Azo Dyes; 2.1.3.3 Carbocyclic Azo Dyes; 2.1.3.4 Heterocyclic Azo Dyes; 2.1.4 References; 2.2 Anthraquinone Chromophore; 2.2.1 Introduction; 2.2.2 General Synthesis; 2.2.3 Principal Properties; 2.2.3.1 Benzodifuranone Dyes; 2.2.3.2 Polycyclic Aromatic Carbonyl Dyes; 2.2.4 References; 2.3 Indigoid Chromophore; 2.3.1 Introduction; 2.3.2 General Synthesis; 2.3.3 Principal Properties; 2.3.3.1 Color; 2.3.3.2 Basic Chromophore; 2.3.3.3 Solvatochromism; 2.3.3.4 Redox System; 2.3.4 References; 2.4 Cationic Dyes as Chromophores 2.4.1 Introduction2.4.2 General Synthesis; 2.4.3 Chemical Structure and Classification; 2.4.3.1 Dyes with Delocalized Charge; 2.4.3.2 Dyes with Localized Charge; 2.4.4 Principal Properties; 2.4.4.1 Cationic Dyes for Synthetic Fibers; 2.4.4.2 Cationic Dyes for Paper, Leather, and Other Substrates; 2.4.5 References; 2.5 Polymethine and Related Chromophores; 2.5.1 Introduction; 2.5.2 General Synthesis; 2.5.3 Principal Properties and Classification; 2.5.3.1 Azacarbocyanines; 2.5.3.2 Hemicyanines; 2.5.3.3 Diazahemicyanines; 2.5.3.4 Styryl Dyes; 2.6 Di- and Triarylcarbenium and Related Chromophores 2.6.1 Introduction2.6.2 Chromophores; 2.6.3 General Synthesis; 2.6.4 Principal Properties; 2.6.5 References; 2.7 Phthalocyanine Chromophore; 2.7.1 Introduction; 2.7.2 General Synthesis; 2.7.3 Principal Properties; 2.7.4 Industrial Production; 2.7.4.1 Copper Phthalocyanine; 2.7.4.2 Phthalocyanine Derivatives; 2.7.4.3 Pthalocyanine Sulfonic Acids and Sulfonyl Chlorides; 2.7.5 References; 2.8 Sulfur Compounds as Chromophores; 2.8.1 Introduction; 2.8.2 Chromophores; 2.8.3 General Synthesis; 2.8.3.1 Sulfur Bake and Polysulfide Bake Dyes; 2.8.3.2 Polysulfide Melt Dyes; 2.8.3.3 Pseudo Sulfur Dyes 2.8.4 Principal Properties2.8.5 References; 2.9 Metal Complexes as Chromophores; 2.9.1 Introduction; 2.9.2 Azo/Azomethine Complex Dyes; 2.9.2.1 General Synthesis; 2.9.2.2 Principal Properties; 2.9.3 Formazan Dyes; 2.9.3.1 Introduction; 2.9.3.2 General Synthesis; 2.9.3.3 Principal Properties; 2.9.4 References; 2.10 Fluorescent Dyes; 2.11 Other Chromophores; 2.11.1 Quinophthalone Dyes; 2.11.2 Nitro and Nitroso Dyes; 2.11.3 Stilbene Dyes; 2.11.4 Formazan Dyes; 2.11.5 Triphenodioxazine Dyes; 2.11.6 References; 3 Dye Classes For Principal Applications; 3.1 Reactive Dyes; 3.1.1 Introduction 3.1.2 Chemical Constitution of Reactive Systems |
Record Nr. | UNINA-9910146244403321 |
Weinheim, : Wiley-VCH, c2003 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Industrial dyes : chemistry, properties, applications / / Klaus Hunger (editor) |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2003 |
Descrizione fisica | 1 online resource (686 p.) |
Disciplina | 667/.25 |
Altri autori (Persone) | HungerKlaus |
Soggetto topico |
Dyes and dyeing - Chemistry
Dyes and dyeing - Industrial applications |
ISBN |
3-527-60606-8
9786612118388 1-282-11838-2 1-280-56073-8 9786610560738 3-527-60201-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Industrial Dyes Chemistry, Properties, Applications; Contents; Preface; List of Contributors; 1 Dyes, General Survey; 1.1 Introduction; 1.2 Classification Systems for Dyes; 1.3 Classification of Dyes by Use or Application Method; 1.4 Nomenclature of Dyes; 1.5 Equipment and Manufacture; 1.6 Economic Aspects; 1.7 References; 2 Important Chemical Chromophores of Dye Classes; Introduction; 2.1 Azo Chromophore; 2.1.1 Introduction; 2.1.2 General Synthesis; 2.1.2.1 Diazo Components; 2.1.2.2 Diazotization Methods; 2.1.2.3 Coupling Components; 2.1.2.4 Azo Coupling in Practice
2.1.3 Principal Properties2.1.3.1 Tautomerism; 2.1.3.2 Metallized Azo Dyes; 2.1.3.3 Carbocyclic Azo Dyes; 2.1.3.4 Heterocyclic Azo Dyes; 2.1.4 References; 2.2 Anthraquinone Chromophore; 2.2.1 Introduction; 2.2.2 General Synthesis; 2.2.3 Principal Properties; 2.2.3.1 Benzodifuranone Dyes; 2.2.3.2 Polycyclic Aromatic Carbonyl Dyes; 2.2.4 References; 2.3 Indigoid Chromophore; 2.3.1 Introduction; 2.3.2 General Synthesis; 2.3.3 Principal Properties; 2.3.3.1 Color; 2.3.3.2 Basic Chromophore; 2.3.3.3 Solvatochromism; 2.3.3.4 Redox System; 2.3.4 References; 2.4 Cationic Dyes as Chromophores 2.4.1 Introduction2.4.2 General Synthesis; 2.4.3 Chemical Structure and Classification; 2.4.3.1 Dyes with Delocalized Charge; 2.4.3.2 Dyes with Localized Charge; 2.4.4 Principal Properties; 2.4.4.1 Cationic Dyes for Synthetic Fibers; 2.4.4.2 Cationic Dyes for Paper, Leather, and Other Substrates; 2.4.5 References; 2.5 Polymethine and Related Chromophores; 2.5.1 Introduction; 2.5.2 General Synthesis; 2.5.3 Principal Properties and Classification; 2.5.3.1 Azacarbocyanines; 2.5.3.2 Hemicyanines; 2.5.3.3 Diazahemicyanines; 2.5.3.4 Styryl Dyes; 2.6 Di- and Triarylcarbenium and Related Chromophores 2.6.1 Introduction2.6.2 Chromophores; 2.6.3 General Synthesis; 2.6.4 Principal Properties; 2.6.5 References; 2.7 Phthalocyanine Chromophore; 2.7.1 Introduction; 2.7.2 General Synthesis; 2.7.3 Principal Properties; 2.7.4 Industrial Production; 2.7.4.1 Copper Phthalocyanine; 2.7.4.2 Phthalocyanine Derivatives; 2.7.4.3 Pthalocyanine Sulfonic Acids and Sulfonyl Chlorides; 2.7.5 References; 2.8 Sulfur Compounds as Chromophores; 2.8.1 Introduction; 2.8.2 Chromophores; 2.8.3 General Synthesis; 2.8.3.1 Sulfur Bake and Polysulfide Bake Dyes; 2.8.3.2 Polysulfide Melt Dyes; 2.8.3.3 Pseudo Sulfur Dyes 2.8.4 Principal Properties2.8.5 References; 2.9 Metal Complexes as Chromophores; 2.9.1 Introduction; 2.9.2 Azo/Azomethine Complex Dyes; 2.9.2.1 General Synthesis; 2.9.2.2 Principal Properties; 2.9.3 Formazan Dyes; 2.9.3.1 Introduction; 2.9.3.2 General Synthesis; 2.9.3.3 Principal Properties; 2.9.4 References; 2.10 Fluorescent Dyes; 2.11 Other Chromophores; 2.11.1 Quinophthalone Dyes; 2.11.2 Nitro and Nitroso Dyes; 2.11.3 Stilbene Dyes; 2.11.4 Formazan Dyes; 2.11.5 Triphenodioxazine Dyes; 2.11.6 References; 3 Dye Classes For Principal Applications; 3.1 Reactive Dyes; 3.1.1 Introduction 3.1.2 Chemical Constitution of Reactive Systems |
Record Nr. | UNINA-9910877581203321 |
Weinheim, : Wiley-VCH, c2003 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|