Foreword |
|
xv | |
Preface |
|
xvii | |
|
1 Genesis of Green Chemistry |
|
|
1 | (32) |
|
|
|
|
|
|
1 | (2) |
|
|
3 | (5) |
|
1.3 Need for Green Chemistry: The Whys and Wherefores |
|
|
8 | (3) |
|
1.4 Designing of the 12 Principles of Green Chemistry |
|
|
11 | (9) |
|
1.5 Green Chemistry and Sustainable Development |
|
|
20 | (2) |
|
1.6 Parameters to Evaluate Chemical Processes: E-Factor and LCA |
|
|
22 | (3) |
|
|
25 | (3) |
|
1.7.1 Atom-Economical Reactions |
|
|
27 | (1) |
|
1.7.2 Atom-Uneconomical Reactions |
|
|
27 | (1) |
|
1.8 Hazards and Risks in Chemistry |
|
|
28 | (1) |
|
|
29 | (1) |
|
|
29 | (4) |
|
2 Waste: A Misplaced Resource |
|
|
33 | (46) |
|
|
|
|
|
33 | (4) |
|
2.2 Sources of Waste Generation |
|
|
37 | (14) |
|
2.2.1 Chemical Wastes Generated from Industrial and Academic Sectors |
|
|
37 | (1) |
|
2.2.1.1 Pharmaceutical wastes |
|
|
37 | (6) |
|
2.2.1.2 Wastes from the academic research sector |
|
|
43 | (1) |
|
|
44 | (3) |
|
|
47 | (3) |
|
|
50 | (1) |
|
2.3 Problems Associated with the Generation and Mismanagement of Waste |
|
|
51 | (2) |
|
2.3.1 Global Case Studies Reflecting Mismanagement of Waste |
|
|
53 | (1) |
|
2.3.1.1 Minamata mercury poisoning incident |
|
|
53 | (1) |
|
|
53 | (8) |
|
2.4.1 Biomass: A Renewable Feedstock |
|
|
57 | (1) |
|
|
58 | (1) |
|
2.4.3 Polymers from Renewable Raw Materials: Thinking Green |
|
|
59 | (1) |
|
|
60 | (1) |
|
|
61 | (1) |
|
2.5 Waste Minimization Techniques |
|
|
61 | (11) |
|
2.5.1 Minimizing the Use of Derivatives in Chemical Processes: A Way toward Improving the Environmental Credentials of Chemical Synthesis |
|
|
61 | (2) |
|
|
63 | (1) |
|
|
64 | (1) |
|
2.5.2.1 Recycling reagents in chemical industries and laboratories |
|
|
65 | (3) |
|
|
68 | (2) |
|
2.5.4 Reduce, Reuse, and Recycle |
|
|
70 | (1) |
|
|
71 | (1) |
|
|
71 | (1) |
|
|
72 | (1) |
|
2.6 Design for Degradation |
|
|
72 | (2) |
|
|
74 | (1) |
|
|
74 | (1) |
|
|
75 | (4) |
|
3 Catalysis: A Promising Green Technology |
|
|
79 | (40) |
|
|
|
|
|
|
79 | (10) |
|
3.1.1 What Is a Catalyst? |
|
|
80 | (1) |
|
3.1.2 History of Catalysis |
|
|
81 | (1) |
|
3.1.3 Catalytic Route vs. Stoichiometric Route: The Greener Aspect |
|
|
82 | (6) |
|
3.1.4 Nobel Prize Awards in the Development of Catalysis |
|
|
88 | (1) |
|
|
89 | (1) |
|
3.3 Next-Generation Catalysts |
|
|
90 | (1) |
|
3.4 Classification of Catalysts |
|
|
91 | (1) |
|
3.5 Homogeneous Catalysis |
|
|
91 | (3) |
|
3.5.1 Hydroformylation Reaction |
|
|
91 | (1) |
|
3.5.2 Olefin Hydrogenation Using Wilkinson's Catalyst |
|
|
92 | (1) |
|
3.5.3 Monsanto and Cativa Process |
|
|
92 | (1) |
|
3.5.4 Reppe Carbonylation Process |
|
|
93 | (1) |
|
|
94 | (1) |
|
3.6 Heterogeneous Catalysis |
|
|
94 | (6) |
|
3.6.1 Haber-Bosch Process |
|
|
95 | (1) |
|
3.6.2 Ziegler-Natta Polymerization |
|
|
96 | (1) |
|
|
96 | (1) |
|
|
97 | (1) |
|
3.6.5 Catalytic Converters |
|
|
97 | (3) |
|
3.7 Phase Transfer Catalysts |
|
|
100 | (3) |
|
|
103 | (1) |
|
3.9 Nanocatalysis: Emerging Hybrid Catalysis |
|
|
104 | (8) |
|
3.9.1 What Is Nanocatalysis? |
|
|
104 | (1) |
|
3.9.2 Synthetic Approaches |
|
|
105 | (1) |
|
3.9.3 Catalytic Applications |
|
|
106 | (1) |
|
3.9.3.1 Metal nanoparticles |
|
|
106 | (3) |
|
3.9.3.2 Metal oxide nanoparticles |
|
|
109 | (1) |
|
3.9.3.3 Magnetic nanoparticles |
|
|
110 | (2) |
|
|
112 | (1) |
|
3.11 Current Challenges and Future Development in Catalysis |
|
|
113 | (1) |
|
|
113 | (1) |
|
|
114 | (5) |
|
4 Alternative Reaction Media |
|
|
119 | (42) |
|
|
|
|
|
119 | (1) |
|
|
120 | (1) |
|
4.3 Problems Related to Traditional Solvent Use |
|
|
120 | (2) |
|
4.4 Criteria for the Selection of Green Solvents |
|
|
122 | (2) |
|
4.5 Green Solvents for Organic Synthesis |
|
|
124 | (27) |
|
|
124 | (5) |
|
4.5.2 Supercritical Fluids |
|
|
129 | (1) |
|
4.5.2.1 Introduction to supercritical fluids |
|
|
129 | (2) |
|
4.5.2.2 Properties of supercritical fluids |
|
|
131 | (1) |
|
4.5.2.3 Supercritical CO2 (Tc = 31.1°C, Pc = 73.8 bar) |
|
|
132 | (2) |
|
4.5.2.4 Supercritical H2O (Tc = 374.2°C, Pc= 220.5 bar) |
|
|
134 | (1) |
|
|
135 | (1) |
|
4.5.3.1 Introduction to ionic liquids |
|
|
135 | (1) |
|
4.5.3.2 Properties of ionic liquids |
|
|
136 | (1) |
|
4.5.3.3 Ionic liquids as solvents |
|
|
137 | (2) |
|
4.5.4 Polyethylene Glycols |
|
|
139 | (2) |
|
|
141 | (1) |
|
4.5.6 Solvents Obtained from Renewable Resources |
|
|
142 | (1) |
|
|
143 | (2) |
|
4.5.6.2 2-Methyltetrahydrofuran |
|
|
145 | (1) |
|
|
146 | (1) |
|
|
147 | (1) |
|
4.5.7 Fluorous Biphasic Solvents |
|
|
148 | (1) |
|
4.5.7.1 Introduction to fluorous biphasic solvents |
|
|
148 | (1) |
|
4.5.7.2 Advantages of using fluorous solvents |
|
|
148 | (1) |
|
4.5.7.3 Fluorous biphasic system as a reaction media |
|
|
149 | (2) |
|
4.6 Solvent-Free Synthesis |
|
|
151 | (3) |
|
4.6.1 When At Least One of the Reactants Is a Liquid |
|
|
151 | (1) |
|
4.6.2 Gas-Phase Catalytic Reactions |
|
|
152 | (1) |
|
4.6.3 Solid-Solid Reaction |
|
|
152 | (1) |
|
4.6.4 Benefits of Solvent-Free Synthesis |
|
|
153 | (1) |
|
|
154 | (1) |
|
|
155 | (2) |
|
|
157 | (4) |
|
5 Greening Energy Sources |
|
|
161 | (44) |
|
|
|
|
|
161 | (3) |
|
5.2 Microwave as a Greener Energy Source |
|
|
164 | (9) |
|
5.2.1 Mechanism of Microwave Heating |
|
|
164 | (1) |
|
5.2.1.1 What makes microwave technology superior to conventional heating? |
|
|
165 | (2) |
|
5.2.2 Microwave-Assisted Chemical Reactions |
|
|
167 | (1) |
|
5.2.2.1 Non-solid-state reactions |
|
|
167 | (4) |
|
5.2.2.2 Solid-state reactions |
|
|
171 | (2) |
|
5.2.3 Challenges Faced by Microwave Technology |
|
|
173 | (1) |
|
5.3 Chemistry Using Ultrasonic Energy |
|
|
173 | (7) |
|
5.3.1 How Sonochemistry Works |
|
|
175 | (1) |
|
5.3.2 Factors Affecting the Cavitation Effect |
|
|
176 | (1) |
|
5.3.3 Sonochemistry for Efficient Organic Synthesis |
|
|
177 | (2) |
|
5.3.4 Applications in Wastewater Treatment |
|
|
179 | (1) |
|
5.3.5 Challenges Faced by Sonochemical Processes |
|
|
180 | (1) |
|
5.4 Visible Light-Driven Processes: Photochemistry |
|
|
180 | (12) |
|
5.4.1 Classification of Photocatalysts |
|
|
181 | (1) |
|
5.4.2 Basic Principle of Photochemistry |
|
|
181 | (1) |
|
5.4.3 Photocatalytic Organic Transformations |
|
|
182 | (1) |
|
5.4.3.1 Photochemical cycloaddition reactions |
|
|
183 | (1) |
|
5.4.3.2 Photoinduced isomerization |
|
|
184 | (1) |
|
5.4.3.3 Photodimerization effect in water |
|
|
184 | (1) |
|
5.4.4 Industrial Applications of Photochemistry |
|
|
185 | (1) |
|
|
185 | (1) |
|
5.4.4.2 Photo-oxygenation |
|
|
185 | (1) |
|
5.4.5 Advantages of Photochemistry |
|
|
186 | (1) |
|
5.4.6 Photocatalytic Degradation of Organic Pollutants |
|
|
187 | (1) |
|
5.4.6.1 Mechanism of photocatalytic degradation of organic pollutants |
|
|
188 | (1) |
|
5.4.7 Factors Affecting Photocatalytic Degradation |
|
|
189 | (1) |
|
5.4.7.1 Effect of the concentration of organic pollutants |
|
|
189 | (1) |
|
5.4.7.2 Effect of the catalyst amount |
|
|
190 | (1) |
|
|
190 | (1) |
|
5.4.7.4 Size, structure, and surface area of the photocatalyst |
|
|
190 | (1) |
|
5.4.7.5 Effect of the reaction temperature |
|
|
190 | (1) |
|
5.4.7.6 Effect of the light intensity and wavelength of irradiation |
|
|
191 | (1) |
|
5.4.8 Challenges Faced by Photochemical Synthesis |
|
|
191 | (1) |
|
5.5 Electrochemistry for Clean Synthesis |
|
|
192 | (7) |
|
5.5.1 Basis of Electrochemical Synthesis |
|
|
193 | (1) |
|
5.5.2 Types of Organic Electrochemical Synthesis |
|
|
194 | (1) |
|
5.5.2.1 Anodic oxidative processes |
|
|
194 | (1) |
|
5.5.2.2 Cathodic reductive processes |
|
|
194 | (1) |
|
5.5.2.3 Paired organic electrosynthesis |
|
|
194 | (1) |
|
5.5.3 Examples of Electrochemical Synthesis |
|
|
195 | (1) |
|
5.5.3.1 Anodic oxidations |
|
|
195 | (1) |
|
5.5.3.2 Cathodic reductions |
|
|
196 | (1) |
|
5.5.3.3 Paired organic electrosynthesis |
|
|
197 | (1) |
|
5.5.4 Advantages of Electrochemical Synthesis |
|
|
198 | (1) |
|
5.5.5 Challenges Faced by Electrochemical Synthesis |
|
|
199 | (1) |
|
|
199 | (1) |
|
|
199 | (1) |
|
|
200 | (5) |
|
6 Implementation of Green Chemistry: Real-World Case Studies |
|
|
205 | (58) |
|
|
|
|
|
205 | (1) |
|
6.2 Synthesis of Valuable Compounds: Greener Protocols |
|
|
206 | (7) |
|
6.2.1 Synthesis of Adipic Acid and Catechol |
|
|
207 | (1) |
|
6.2.2 Synthesis of Styrene |
|
|
208 | (1) |
|
6.2.3 Synthesis of Citral |
|
|
209 | (1) |
|
6.2.4 Synthesis of Disodium Iminodiacetate |
|
|
210 | (1) |
|
6.2.5 Synthesis of Acetaldehyde |
|
|
211 | (1) |
|
6.2.6 Synthesis of Urethane |
|
|
211 | (1) |
|
6.2.7 Selective Methylation of Active Methylene Using Dimethyl Carbonate |
|
|
212 | (1) |
|
6.3 Some Real-World Cases: Green Chemistry Efforts Honored |
|
|
213 | (38) |
|
6.3.1 Development of NatureWorks™ PLA: An Efficient, Green Synthesis of a Biodegradable and Widely Applicable Plastic Made from Corn (A Renewable Resource) |
|
|
214 | (1) |
|
6.3.1.1 Greener alternative: Polylactic acid |
|
|
215 | (1) |
|
6.3.1.2 NatureWorks LLC: Synthesizing PLA from corn |
|
|
215 | (4) |
|
6.3.2 Healthier Fats and Oils via a Greener Route: Enzymatic Interesterification for the Production of Trans-Free Fats and Oils |
|
|
219 | (3) |
|
6.3.2.1 Green chemistry: Interesterification of oils |
|
|
222 | (1) |
|
6.3.2.2 Enzymatic interesterification of oils |
|
|
223 | (1) |
|
6.3.3 Development of Fully Recyclable Carpet: Cradle-to-Cradle Carpeting |
|
|
224 | (1) |
|
6.3.3.1 Green chemistry: Production of a cradle-to-cradle carpet |
|
|
225 | (1) |
|
6.3.3.2 Recycling of PO-backed nylon-faced carpeting |
|
|
226 | (1) |
|
6.3.4 Design and Development of Environmentally Safe Marine Antifoulant |
|
|
226 | (2) |
|
6.3.4.1 Development of SeaNine™ 211: Environmentally safe antifoulant |
|
|
228 | (2) |
|
6.3.5 Designing Rightfit™ Pigments to Replace Toxic Organic and Inorganic Pigments |
|
|
230 | (1) |
|
6.3.5.1 Green chemistry innovation |
|
|
231 | (1) |
|
6.3.5.2 Issues underlying and resolved |
|
|
231 | (2) |
|
6.3.5.3 How the Rightfit™ pigments can be synthesized |
|
|
233 | (2) |
|
6.3.6 Design and Application of Surfactants for CO2 Replacing Smog-Producing and Ozone-Depleting Solvents for Precision Cleaning and Service Industry |
|
|
235 | (1) |
|
6.3.6.1 CO2 as a greener alternative |
|
|
236 | (1) |
|
6.3.6.2 Benefits of scCO2 |
|
|
237 | (1) |
|
6.3.6.3 How does a surfactant work? |
|
|
238 | (1) |
|
6.3.6.4 Green chemistry innovation |
|
|
238 | (1) |
|
6.3.6.5 Mechanism of action |
|
|
239 | (1) |
|
6.3.7 Green Synthesis of Ibuprofen by BHC |
|
|
239 | (1) |
|
6.3.7.1 Green chemistry innovation |
|
|
240 | (1) |
|
6.3.8 TAML Oxidant Activators: General Activation of Hydrogen Peroxide for Green Oxidation Technologies |
|
|
241 | (2) |
|
6.3.8.1 Green chemistry innovation |
|
|
243 | (1) |
|
6.3.9 Simple and Efficient Recycling of Rare Earth Elements from Consumer Materials Using Tailored Metal Complexes |
|
|
244 | (1) |
|
6.3.9.1 Green chemistry innovation |
|
|
245 | (1) |
|
6.3.10 Using Naturally Occurring Protein to Stimulate Plant Growth, Improve Crop Quality, Increase Yields, and Suppress Disease |
|
|
245 | (2) |
|
6.3.10.1 Green chemistry innovation |
|
|
247 | (1) |
|
6.3.10.2 Mechanism of action |
|
|
248 | (1) |
|
6.3.10.3 Advantages of harpin |
|
|
248 | (1) |
|
6.3.11 Environmentally Advanced Wood Preservatives: Replacing Toxic Chromium and Arsenic with Copper and Quaternary Ammonium Compounds |
|
|
249 | (1) |
|
6.3.11.1 Green chemistry: Removing arsenic and chromium from PTW |
|
|
250 | (1) |
|
6.4 Need for Industry-Academia Collaboration |
|
|
251 | (4) |
|
6.4.1 An Efficient Biocatalytic Process to Manufacture Simvastatin |
|
|
253 | (2) |
|
6.4.2 Green Route for the Manufacture of Ranitidine |
|
|
255 | (1) |
|
|
255 | (2) |
|
|
257 | (1) |
|
|
257 | (6) |
|
7 Green Chemistry in Education, Practice, and Teaching |
|
|
263 | (20) |
|
|
|
|
|
|
263 | (2) |
|
7.2 Green Chemistry in Classroom |
|
|
265 | (5) |
|
7.3 Green Chemistry in a Teaching Laboratory |
|
|
270 | (4) |
|
7.4 Green Chemistry Institutes and Network Centers |
|
|
274 | (3) |
|
7.5 Important Journals and Websites |
|
|
277 | (3) |
|
|
280 | (1) |
|
|
281 | (1) |
|
|
281 | (2) |
|
8 Green Chemistry: Vision for the Future |
|
|
283 | (38) |
|
|
|
|
|
|
283 | (1) |
|
8.2 Challenges Lying Ahead of Green Chemistry |
|
|
284 | (5) |
|
8.3 Future Directions: Focus of the Future Researchers |
|
|
289 | (1) |
|
8.3.1 Nondepleting Nature |
|
|
289 | (1) |
|
|
289 | (1) |
|
8.3.3 Nonpersistent Nature |
|
|
290 | (1) |
|
8.4 Selective Reagents in Organic Transformations |
|
|
290 | (7) |
|
|
292 | (1) |
|
8.4.2 Dry Media Synthesis |
|
|
292 | (1) |
|
8.4.3 Green Catalysis in Organic Synthesis |
|
|
293 | (2) |
|
8.4.4 Catalyst-Free Reactions in Organic Synthesis |
|
|
295 | (1) |
|
8.4.5 Energy-Efficient Synthesis |
|
|
295 | (2) |
|
|
297 | (3) |
|
8.5.1 Generic Goals of Miniaturization |
|
|
297 | (1) |
|
8.5.2 Miniaturization in Pharmaceutical Industries |
|
|
298 | (1) |
|
8.5.3 Miniaturization in Undergraduate Laboratories |
|
|
299 | (1) |
|
8.6 Biomimetic: Green Chemistry Solution |
|
|
300 | (5) |
|
8.7 Continuous Flow Technology |
|
|
305 | (3) |
|
8.8 Combinatorial Chemical Technology |
|
|
308 | (3) |
|
8.9 Green Chemistry and Sustainability |
|
|
311 | (2) |
|
|
313 | (1) |
|
|
314 | (1) |
|
|
315 | (6) |
Index |
|
321 | |