tailieunhanh - GREEN CHEMISTRY – ENVIRONMENTALLY BENIGN APPROACHES

The environmental legislation contained in the Pollution Prevention Act of 1990 set the stage for green chemistry. Environmental concerns in research and industry are increasing with more and more pressure to reduce the number of pollutants produced. Green chemistry, environmentally benign chemistry and sustainable chemistry involve the design of chemical products and processes that eliminates the use and generation of hazardous substances. So, instead of limiting risk by controlling our exposure to hazardous chemicals, green chemistry attempts to reduce and preferentially eliminate the hazard thus negating the necessity to control exposure | GREEN CHEMISTRY -ENVIRONMENTALLY BENIGN APPROACHES Edited by Mazaahir Kidwai and Neeraj Kumar Mishra Green Chemistry - Environmentally Benign Approaches Edited by Mazaahir Kidwai and Neeraj Kumar Mishra Published by InTech Janeza Trdine 9 51000 Rijeka Croatia Copyright 2012 InTech All chapters are Open Access distributed under the Creative Commons Attribution license which allows users to download copy and build upon published articles even for commercial purposes as long as the author and publisher are properly credited which ensures maximum dissemination and a wider impact of our publications. After this work has been published by InTech authors have the right to republish it in whole or part in any publication of which they are the author and to make other personal use of the work. Any republication referencing or personal use of the work must explicitly identify the original source. As for readers this license allows users to download copy and build upon published chapters even for commercial purposes as long as the author and publisher are properly credited which ensures maximum dissemination and a wider impact of our publications. Notice Statements and opinions expressed in the chapters are these of the individual contributors and not necessarily those of the editors or publisher. No responsibility is accepted for the accuracy of information contained in the published chapters. The publisher assumes no responsibility for any damage or injury to persons or property arising out of the use of any materials instructions methods or ideas contained in the book. Publishing Process Manager Ivona Lovric Technical Editor Teodora Smiljanic Cover Designer InTech Design Team First published March 2012 Printed in Croatia A free online edition of this book is available at Additional hard copies can be obtained from orders@ Green Chemistry - Environmentally Benign Approaches Edited by Mazaahir Kidwai and Neeraj Kumar Mishra

• Điện - Điện tử
• Green Chemistry
• Application of Nanometals
• Green Synthesis
• Green Conversion
• Ultrasound Assisted
• Green Sy
• Methods and reagents for green chemistry
• The Four Component reaction
• Other multicomponent reactions
• Dimethyl carbon
• Reagents for green chemistry
• Enantioselective metal cata lyzed oxidat ion processes
• Cleaner technologies
• Zeolite catalysts
• Industrial green chemistry
• Journal of Science and Technology
• Green organic synthesis of N methylpyrrolidine
• Gas Chromatography Mass spectroscopy
• The green chemistry process
• Via the green chemistry process
• Journal of Chemistry
• Separation preconcentration
• Liquid phase microextraction
• Solvent microextraction
• Sample preparation
• Green solvent
• Multicomponent domino reactions
• Microwave irradiation
• Benzo[a]chromeno[2 3 c]phenazine
• Aromatic aldehydes
• BMC Chemistry
• Green coffee beans
• Fluorescence spectroscopy
• Analytical methods
• NIR spectroscopy
• Pyrrolidinone derivatives
• One pot multi component reaction
• 2 Pyrrolidinone derivatives
• Green chemistry towards
• Nuclear magnetic resonance
• Heavy metals
• Cetylpyridinium chloride
• Analytical chemistry
• Heck reactions of aryl halides with styrene
• 1 butyl 3 methylimidazolium bromide ionic liquid
• Green solvent under microwave irradiation
• The Heck cross coupling reaction
• The principal products
• Suzuki reactions of aryl halides with phenylboronic acid
• Suzuki reactions of aryl halides
• Imidazolium based ionic liquid
• Green catalyst
• Ionic liquids
• Knoevenagel reaction
• Methylimidazolium hydroxide
• Bio based support
• Click reaction
• Heterogeneous catalyst
• Peanut shell
• Ultrasonic irradiation
• UV–VIS spectroscopy
• Water extract
• Malachite green
• Teak leaf litter
• Teak leaf litter powde
• Langmuir isotherm
• JAK2 inhibitor
• Microchannel reactor
• Anti infammatory activity
• Boric acid
• Solvent free
• Green method
• 2 amino 4 6 diarylnicotinonitrile
• Single crystal
• Malachite green adsorption
• ZnO/aminated SWCNT COOH nanocomposite
• Response surface methodology
• Preparation of nanocomposite
• Poly(malachite green)
• Multiwalled carbon nanotubes
• Cyclic voltammetry (CV)
• Differential pulse voltammetry (DPV)
• Thioformamide derivatives
• Environmentally green synthesis
• Multicomponent reactions (MCRs)
• Mesoionic rhodanine
• Magnetic nanomaterials
• Magnetic properties
• Electromagnetic interface (EMI)
• Green emission
• Cross linking
• Conjugated polymers
• Oligo(azomethine ether)
• Polymeric light emitting diodes (PLEDs)
• Antimicrobial action
• Toxicity analysis
• Multicomponent nanomaterials
• Metal supported nanomaterials
• Mesoporous materials
• Natural compounds
• High value added chemicals
• Organic syntheses
• H2SO4 modified clinoptilolite
• Turkish Journal of Chemistry
• Tạp chí Hóa học
• Green synthesized
• Salvia officinalis
• Thymus vulgaris
• Biological properties