Industrial organic chemistry / / Klaus Weissermel, Hans-Jürgen Arpe

• Autore: Weissermel Klaus
• Pubblicazione: Weinheim, Germany ; ; New York, New York : , : John Wiley & Sons, , [1997]; ©1997
• Edizione: Third edition.
• Descrizione fisica: 1 online resource (xvii, 464 pages)
• Disciplina: 661/.8
• Soggetto topico: Chemistry, Technical; Chemistry, Organic
• Persona (resp. second.): ArpeHans-Jürgen
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references (pages [428]-438) and index.
• Nota di contenuto: Industrial Organic Chemistry; Contents; 1 . Various Aspects of the Energy and Raw Material Supply; 1.1. Present and Predictable Energy Requirements; 1.2. Availability of Individual Sources; 1.2.1. Oil; 1.2.2. Natural Gas; 1.2.3. Coal; 1.2.4. Nuclear Fuels; 1.3. Prospects for the Future Energy Supply; 1.4. Present and Anticipated Raw Material Situation; 1.4.1. Petrochemical Primary Products; 1.4.2. Coal Conversion Products; 2 . Basic Products of Industrial Syntheses; 2.1. Synthesis Gas; 2.1.1. Generation of Synthesis Gas; 2.1.1.1. Synthesis Gas via Coal Gasification ; 2.1.1.2. Synthesis Gas via Cracking of Natural Gas and Oil2.1.2. Synthesis Gas Purification and Use; 2.2. Production of the Pure Synthesis Gas Components; 2.2.1. Carbon Monoxide; 2.2.2. Hydrogen; 2.3. C1-Units; 2.3.1.Methanol; 2.3.1.1. Manufacture of Methanol; 2.3.1.2. Applications and Potential Applications of Methanol; 2.3.2. Formaldehyde; 2.3.2.1. Formaldehyde from Methanol; 2.3.2.2. Uses and Potential Uses of Formaldehyde; 2.3.3. Formic Acid; 2.3.4. Hydrocyanic Acid; 2.3.5.Methylamines; 2.3.6. Halogen Derivatives of Methane; 2.3.6.1. Chloromethanes; 2.3.6.2. Chlorofluoromethanes ; 3 . Olefins3.1. Historical Development of Olefin Chemistry; 3.2. Olefins via Cracking of Hydrocarbons; 3.3. Special Manufacturing Processes for Olefins; 3.3.1. Ethylene, Propene; 3.3.2. Butenes; 3.3.3. Higher Olefins; 3.3.3.1. Unbranched Higher Olefins; 3.3.3.2. Branched Higher Olefins; 3.4. Olefin Metathesis; 4 . Acetylene; 4.1. Present Significance of Acetylene; 4.2. Manufacturing Processes for Acetylene; 4.2.1. Manufacture Based on Calcium Carbide; 4.2.2. Thermal Processes; 4.3. Utilization of Acetylene; 5. 1, 3 -Diolefins; 5.1. 1, 3-Butadiene ; 5.1.1. Traditional Syntheses of 1,3-Butadiene5.1.2. 1, 3-Butadiene from C4 Cracking Fractions; 5.1.3. 1, 3-Butadiene from C4 Alkanes and Alkenes; 5.1.4. Utilization of 1,3-Butadiene; 5.2. Isoprene; 5.2.1. Isoprene from C5 Cracking Fractions; 5.2.2. Isoprene from Synthetic Reactions; 5.3. Chloroprene; 5.4. Cyclopentadiene; 6 . Syntheses Involving Carbon Monoxide; 6.1.Hydroformylation of Olefins; 6.1.1. The Chemical Basis of Hydroformylation; 6.1.2. Industrial Operation of Hydroformylation; 6.1.3. Catalyst Modifications in Hydroformylation; 6.1.4. Utilization of 'Oxo' Products ; 6.1.4.1. 'Oxo' Alcohols6.1.4.2.'Oxo' Carboxylic Acids; 6.1.4.3. Aldol and Condensation Products of The 'Oxo' Aldehydes; 6.2. Carbonylation of Olefins; 6.3. The Koch Carboxylic Acid Synthesis; 7 . Oxidation Products of Ethylene; 7.1. Ethylene Oxide; 7.1.1. Ethylene Oxide by Chlorohydrin Process; 7.1.2. Ethylene Oxide by Direct Oxidation; 7.1.2.1. Chemical Principles; 7.1.2.2. Process Operation; 7.1.2.3. Potential Developments in Ethylene Oxide Manufacture; 7.2. Secondary Products of Ethylene Oxide; 7.2.1. Ethylene Glycol and Higher Ethylene Glycols ; 7.2.1.1. Potential Developments in Ethylene Glycol Manufacture
• Sommario/riassunto: 'Ideal for getting an overview of applied organic chemistry'This bestselling standard, now in its 3rd completely revised English edition, is an excellent source of technological and economic information on the most important precursors and intermediates used in the chemical industry. Right and left columns containing synopsis of the main text and statistical data, and numerous fold-out flow diagrams ensure optimal didactic presentation of complex chemical processes.The translation into eight languages, the four German and three English editions clearly evidence the popularity of th
• Titolo autorizzato: Industrial organic chemistry
• ISBN: 1-281-75845-0; 3-527-61459-1; 9786611758455; 3-527-61668-3
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 996212582503316
• Lo trovi qui: Univ. di Salerno