Chemistry Beyond Chlorine by Pietro TundoChemistry Beyond Chlorine by Pietro Tundo

Chemistry Beyond Chlorine

byPietro TundoEditorLiang-Nian He, Ekaterina Lokteva

Paperback | April 22, 2018

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Since the industrial revolution, chlorine remains an iconic molecule even though its production by the electrolysis of sodium chloride is extremely energy intensive. The rationale behind this book is to present useful and industrially relevant examples for alternatives to chlorine in synthesis. This multi-authored volume presents numerous contributions from an international spectrum of authors that demonstrate how to facilitate the development of industrially relevant and implementable breakthrough technologies. This volume will interest individuals working in organic synthesis in industry and academia who are working in Green Chemistry and Sustainable Technologies.

Pietro Tundo, Editor, is Full Professor of Organic Chemistry at the University of Venice. He has published over 200 scientific articles, one book, and holds twenty-five patents. His research on Clean Processes led to the development of Gas-Liquid Phase-Transfer Catalysis, a method for the synthesis of Non-Steroidal Anti-inflammatory Dr...
Title:Chemistry Beyond ChlorineFormat:PaperbackDimensions:608 pages, 23.5 × 15.5 × 0.17 inPublished:April 22, 2018Publisher:Springer NatureLanguage:English

The following ISBNs are associated with this title:

ISBN - 10:331980717X

ISBN - 13:9783319807171


Table of Contents

PhilipHodge , A Green Method for Potentially Recycling Condensation Polymers: Ring-chain Recycling.- AttilioCitterio , Green syntheses of bicarboxylic acids for polymer manufactures.- CarloPerego , Zeolites as catalysts for MDA synthesis and DMC as reagent for MDI e TDI manufacture.- MarcellaFernandes de Souza , Ricardo Sposina Sobral Teixeira, Ayla Sant'Ana da Silva, Viridiana Santana Ferreira-Leitão, Elba Pinto da Silva Bon, Chlorine-free biomass processing: enzymatic alternatives for bleaching and hydrolysis of lignocellulosic materials.- YehudaShevah , Substitution of chloride chemicals with degradable bio-flocculants for sedimentation of suspended particles in water.- EkaterinaLokteva , Elena Golubina, Vladimir Likholobov and Valery Lunin, Disposal of chlorine-containing wastes.- Claudio J. A.Mota , Chlorine-Free Heterogeneous Acid Catalysts.- YuryTreger and Mark Flid, Chloroorganic synthesis: Problems? Outlook!.- Aziz Muzafarov, Polymers beyond chlorine.- ShouyingHuang , Yuanyuan Dong, Shengping Wang, Xinbin Ma, Chlorine-Free Catalysis for the Synthesis of Dialkyl Carbonate via Oxidative Carbonylation of alcohols.- Mei-YanWang , Hai-Bo Wang, Qiang-Hao Qu, Liang-Nian He, Industrial Production of Dimethyl Carbonate from CO2 in China.- BinshenWang , Elnazeer H. M. Elageed, Guohua Gao, Organic Carbonates Transformation Catalyzed by Ionic Liquids.- Shin-ichiroFujita , Hiroshi Yoshida, Masahiko Arai, Synthesis of Carbonate Compounds Using Carbon Dioxide and Carbon Dioxide - Derived Materials.- ZhongweiFu and Yuezhong Meng, Research Progress in the Phosgene-free and Direct Synthesis of Dimethyl Carbonate from CO2 and Methanol.- Qing-WenSong and Liang-Nian He, Heterocyclic Synthesis through C-N Bond Formation with Carbon Dioxide.- HuanwangJing , Beyond Chlorine Reagents: Organic Carbonate Chemistry.- Ian D. V.Ingram , Professor Michael North and Dr. Xiao Wu, Halide free synthesis of cyclic and polycarbonates.- AureliaVisa , Bianca Maranescu, Gheorghe Ilia, Hypophosphorus Acid and its Salts as Reagents in Organophosphorus Chemistry.- MariaCaporali , Manuel Serrano Ruiz, Maurizio Peruzzini, Benign chlorine-free approaches to organophosphorus compounds.- PietroTundo and Fabio Aricò, Dialkyl Carbonates in the synthesis of heterocycles.- JohnAndraos , Application of Green Metrics Analysis to the Synthesis of Dicyclohexylcarbodiimide (DCC) - Comparison of Chlorine versus Non-chlorine Based Routes.- FengWang , Wenbo Liu and Chao-Jun Li, Catalytic Grignard-Type Addition of Aryl C-H Bonds to C=O and C=N Bonds.- Oleg M.Demchuk , Radomir JasiÅski, Adam Formela, The halogenless catalytic transition metal mediated cross-coupling reactions. A sustainable alternative for utilisation of organohalides.