Green Solvents for Chemistry: Perspectives and Practice

Total Page:16

File Type:pdf, Size:1020Kb

Green Solvents for Chemistry: Perspectives and Practice Green Solvents for Chemistry: Perspectives and Practice William M. Nelson OXFORD UNIVERSITY PRESS GREEN SOLVENTS FOR CHEMISTRY This page intentionally left blank Green Solvents for Chemistry Perspectives and Practice William M. Nelson 1 2003 3 Oxford New York Auckland Bangkok Buenos Aires Cape Town Chennai Dar es Salaam Delhi Hong Kong Istanbul Karachi Kolkata Kuala Lumpur Madrid Melbourne Mexico City Mumbai Nairobi Sa˜o Paulo Shanghai Taipei Tokyo Toronto Copyright 2003 by Oxford University Press, Inc. Published by Oxford University Press, Inc. 198 Madison Avenue, New York, New York 10016 www.oup.com Oxford is a registered trademark of Oxford University Press All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without the prior permission of Oxford University Press. Library of Congress Cataloging-in-Publication Data Nelson, William M. Green solvents for chemistry : perspectives and practice / William M. Nelson. p. cm. — (Green chemistry series) Includes bibliographical references and index. ISBN 0-19-515736-2 1. Solvents. 2. Environmental chemistry—Industrial applications. I. Title. II. Series. TP247.5.N42 2003 661′.807—dc21 2002041662 987654321 Printed in the United States of America on acid-free paper For Millie, whose love and support has kept me on track and for Maria, Milee, Liam, and Madeleine, who are my priceless jewels This page intentionally left blank Contents 1. Philosophy of the Environment, 3 1.1 The Emerging Paradigm, 3 1.2 Pollution Prevention and Green Chemistry, 6 1.3 Philosophy in Practice, 11 1.4 Solvents, 13 1.5 Future Direction, 17 1.6 Subject Content of Book, 18 2. Chemical Practice and Solvent Usage, 20 2.1 Solvent Usage, 20 2.2 Pollution: Effects of solvents, 23 2.3 Applications of Solvents, 26 2.4 Broad Areas of Application, 26 2.5 Domain and Range of Solvent Employment, 31 2.6 Global Effects of Solvent Usage, 32 2.7 Challenge Offered to the Chemical Community, 46 2.8 Solvent Supply and Demand, 49 3. Solvation and Solvent Phenomena, 51 3.1 Introduction, 51 3.2 Physical Properties of Solvents, 51 viii Contents 3.3 Chemical Properites of Solvents, 53 3.4 Solvation Chemistry, 60 3.5 Sovent Effects on Chemical Phenomena, 76 3.6 Solvent Roles, 87 3.7 Solvent Effects and Green Chemistry, 89 4. Green Solvents in Green Chemistry, 91 4.1 Definition of Green Solvents, 91 4.2 Specific Health and Environmental Requirements, 94 4.3 Solvents in Terms of Life-Cycle Analysis, 96 4.4 Life-Cycle Assessment, 97 4.5 Life-Cycle Assessment: Its Application to Solvents, 101 4.6 A Proposed LCA Approach to Solvent Selection, 104 4.7 Proposed Checklist for Solvent Use Evaluation, 107 4.8 Practical Approach to Life-Cycle Evaluation of Solvent Usage, 108 4.9 LCA Leading to Total Quality Management (TQM), 109 4.10 Concluding Comments on LCA, 110 4.11 Green Solvents, 111 5. Criteria for Selection and/or Design of Green Solvents, 116 5.1 The Need for Green Solvents, 116 5.2 Criteria to Evaluate Solvents, 119 5.3 Reversibility of Toxicity, 120 5.4 Concept of Receptors, 121 5.5 Mode of Entry of Toxins, 121 5.6 Translocation of Xenobiotics, 123 5.7 Storage of Chemicals in the Body, 124 5.8 Interpretation of Toxicity, 125 5.9 Methodology to Evaluate Green Solvents, 126 5.10 Presently Available Solvents, 129 6. Green Solvents for Academic Chemistry, 133 6.1 Environmental Concerns for Educational Institutions, 133 6.2 Green Chemistry Alternatives, 136 6.3 Early Chemistries: Elementary through High School, 136 6.4 Undergraduate/Graduate Schools, 139 6.5 Organic Chemistry, 142 6.6 Readily Available Drop-in Replacements, 180 6.7 Inorganic Chemistry, 187 6.8 Nuclear and Photochemistry, 188 6.9 Analytical Chemistry, 191 Contents ix 6.10 Biochemistry, 194 6.11 Medicinal Chemistry, 195 6.12 Teaching Laboratories, 196 7. Green Solvents for Industrial Chemistry, 198 7.1 Environmentally Friendly Processes, 198 7.2 Industry’s Response to the Global Environment, 200 7.3 Occupational Toxicology, 202 7.4 What Are Green Industrial Solvents? 207 7.5 Solvents by Industrial Reaction Process, 211 7.6 Alternative Solvents for Separation Processes, 243 7.7 Military Solvents, 245 7.8 Future of Industrial Solvents, 247 8. Green Solvents for Practical and Ordinary Chemical Usage, 252 8.1 Why This Area? 252 8.2 Ordinary Solvent Usage, 255 8.3 Household Solvents, 259 8.4 Recreational and Transportation Solvents, 260 8.5 Evaluating Chemistries, 263 9. Green Solvents: Ecology and Economics, 272 9.1 Place of Green Solvents in Chemistry Practices, 272 9.2 Green Solvents: Epilogue, 273 9.3 Economics and Ecology, 275 9.4 Future Steps, 276 Appendices, 295 References, 345 Author Index, 378 Subject Index, 386 This page intentionally left blank GREEN SOLVENTS FOR CHEMISTRY Knowledge is of two kinds. We know a subject ourselves or we know where we can find information upon it. —Samuel Johnson 1 Philosophy of the Environment 1.1 The Emerging Paradigm Let us put chemical usage in context. There is justifiably a concern over the adverse effects of chemicals on human health and the environment. The source of chemicals may be industrial, commercial, or adventitious. Environmental quality is a concern in the United States and throughout the world. This concern is important today. Our world has heightened environmental awareness, fueled by public interest groups and the media. Public awareness is growing of the processes involved in the use, manufac- turing, and effect of many chemicals on the environment, including the generation of waste, the disruption of ecosystems, and the depletion of natural resources. Current patterns of chemical development threaten to exceed the limits of sustainability in terms of resource utilization and waste management, and also pose potential threats to global climate, vegetation, and agriculture. According to the U.S. Environmental Pro- tection Agency (EPA), about 123 billion tons of industrial wastes are generated annu- ally in the United States, and more than a third of this is hazardous waste. This presents a challenge to the chemical industry. Although the EPA has striven to reduce the impact of toxic chemicals, the efforts have focused primarily on exposure-based approaches. Within the United States, the Pollution Prevention Act of 1990 introduced a new era in regulatory philosophy and policy. The emphasis became the prevention of toxic substances at their source. Green chemistry aims at accomplishing pollution prevention through the design of safer chemicals and the use of more environmentally friendly chemical processes. Green chemistry provides the unifying backbone of this book. Realizing the potential of 3 4 Green Solvents for Chemistry green chemistry will require major changes in the current practices of both academia and industry. Fundamentally, all those associated with the development, manufacture, and use of industrial chemicals must understand green chemistry. New ideas, concepts, and technologies, like green solvents, must replace outdated ones. Designing safer chemicals is essential in today’s chemical environment. “Science is necessary but not sufficient” (Maltoni and Selikoff, 1988), and we must balance the contributions of chemistry with the issues of the broader scientific community, public institutions, industry, and those concerned with ethical and social concerns. Experience reveals that safer chemicals and chemical processes provide competitive advantages by reducing the costs of production and waste management, encouraging innovation in novel chemical syntheses, and developing new markets. The chemical industry faces a major challenge in fully embracing this new paradigm (Wicks and Yeske, 1996). 1.1.1 Background The environment is a complex nexus of interdependent dynamic activities closely related to the internal or external chemistries that support them. Chemists pollute the environment by inducing a change in the supporting chemistry. This occurs when the practice of a human technology jeopardizes any living activities that are recognized to be important (Collins, 1995). The emerging environmental philosophy is a rational reaction to the alarm that pollution has engendered among visionaries such as Rachel Carson who published her alert Silent Spring in 1962 (Carson, 1962). The imperative to attend to global environmental issues includes numerous individuals: government officials and scientists who evaluate and regulate against pollution, commentators who raise public consciousness about pollution, corporate executives who shoulder much of the responsibility for minimizing pollution, and concerned citizens. Chemistry is the tool in the hands of the artisan. However, human activities lead to “randomness.” In other words, our activities tend to leave waste. With the power of science and technology comes a great responsibility not to pollute. While excuses continue to be invented, the proportion of our population who realizes how much we have to change is growing substantially. As a result, our collective energy is being redirected wisely, and this is especially true in the area of chemistry (Anastas, 1996). Chemistry comprises so large a component of modern technology that the develop- ment of green technologies is significantly a chemical enterprise. 1.1.2 Pollution Prevention Pollution prevention (P2) is a bold vision that confronts the global problem of environ- mental pollution. P2 presents an operative paradigm requiring a fundamentally differ- ent approach to the way industry and technologies accomplish their tasks. Waste and pollutants are prevented where they originate. This necessitates changes in manufac- turing technologies and practices, chemicals and other raw materials, and even prod- ucts and packaging. In terms of scientific revolutions, this constitutes a paradigm shift (Kuhn, 1996). The period between 1984 and 1986 marks the beginning of the current P2 move- ment in the United States. Since that time, the pollution prevention idea has grown into a significant international movement.
Recommended publications
  • Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
    NOMENCLATURE OF INORGANIC CHEMISTRY IUPAC Recommendations 2005 IUPAC Periodic Table of the Elements 118 1 2 21314151617 H He 3 4 5 6 7 8 9 10 Li Be B C N O F Ne 11 12 13 14 15 16 17 18 3456 78910 11 12 Na Mg Al Si P S Cl Ar 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe 55 56 * 57− 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 Cs Ba lanthanoids Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn 87 88 ‡ 89− 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 Fr Ra actinoids Rf Db Sg Bh Hs Mt Ds Rg Uub Uut Uuq Uup Uuh Uus Uuo * 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu ‡ 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr International Union of Pure and Applied Chemistry Nomenclature of Inorganic Chemistry IUPAC RECOMMENDATIONS 2005 Issued by the Division of Chemical Nomenclature and Structure Representation in collaboration with the Division of Inorganic Chemistry Prepared for publication by Neil G.
    [Show full text]
  • Organometallic Chemistry and Catalysis Grenoble Sciences
    ATOMIC WEIGHTS OF THE ELEMENTS a, b (adapted from T.B. Coplen et al., Inorg. Chim. Acta 217, 217, 1994) Element Symbol Atomic Atomic Element Symbol Atomic Atomic Number Weight Number Weight Actiniumc 227Ac 89 227.03 Mercury Hg 80 200.59(2) Aluminum Al 13 26.982 Molybdenum Mo 42 95.94 Americiumc Am 95 241.06 Neodynium Nd 60 144.24(3) Antimony Sb 51 121.76 Neon Ne 10 20.180 Argon Ar 18 39.948 Neptuniumc 237Np 93 237.05 Arsenic As 33 74.922 Nickel Ni 28 58.693 Astatinec 210At 85 209.99 Niobium Nb 41 92.906 Barium Ba 56 137.33 Nitrogen N 7 14.007 Berkeliumc 249Bk 97 249.08 Nobeliumc 259No 102 259.10 Beryllium Be 4 9.0122 Osmium Os 76 190.23(3) Bismuth Bi 83 208.98 Oxygen O 8 15.999 Boron B 5 10.811(5) Palladium Pd 46 106.42 Bromine Br 35 79.904 Phosphorus P 15 30.974 Cadmium Cd 48 112.41 Platinum Pt 78 195.08(3) Calcium Ca 20 40.078(4) Plutoniumc 239Pu 94 239.05 Californiumc 232Cf 98 252.08 Poloniumc 210Po 84 209.98 Carbon C 6 12.011 Potassium K 19 39.098 Cerium Ce 58 140.12 Praseodynium Pr 59 140.91 Cesium Cs 55 132.91 Promethiumc 147Pm 61 146.92 Chlorine Cl 17 35.453 Proactiniumc Pa 91 231.04 Chromium Cr 24 51.996 Radiumc 226Ra 88 226.03 Cobalt Co 27 58.933 Radonc 222Rn 86 222.02 Copper Cu 29 63.546(3) Rhenium Re 75 186.21 Curiumc 244Cm 96 244.06 Rhodium Rh 45 102.91 Dysprosiumc Dy 66 162.50(3) Rubidium Rb 37 85.468 Einsteiniumc 252Es 99 252.08 Ruthenium Ru 44 101.07(2) Erbium Er 68 167.26(3) Samarium Sm 62 150.36(3) Europium Eu 63 151.96 Scandium Sc 21 44.956 Fermiumc 257Fm 100 257.1 Selenium Se 34 78.96(3) Fluorine F 9 18.998 Silicon
    [Show full text]
  • Answers to Exercises References Abbreviations
    ANSWERS TO EXERCISES REFERENCES ABBREVIATIONS INDEX ATOMIC WEIGHTS OF THE ELEMENTS PERIODIC TABLE OF THE ELEMENTS ANSWERS TO EXERCISES CHAPTER 1 + + 1.1. [FeCp2] , sandwich structure with parallel rings, [FeL4X2] , 17, 5, 3, 6; [RhCl(PPh3)3], square planar, [RhL3X], 16, 8, 1, 4; [Ta(CH2CMe3)3(CHCMe3)], tetrahedral, [TaX5], 10, 0, 5, 4; [ScCp*2(CH3)], bent sandwich with CH3 in the equatorial plane, [ScL4X3], 14, 0, 3, 7; [HfCp2Cl2], bent sandwich with both Cl ligands in the equatorial plane, [HfL4X4], 16, 0, 4, 8; – – [W(H)(CO)5] , octahedral, [WL5X] , 18, 6, 0, 6; 2 2+ 2+ [Os(NH3)5( -C6H6)] , octahedral, [OsL6] , 18, 6, 2, 6; [Ir(CO)(PPh3)2(Cl)], square planar, [IrL3X], 16, 8, 1, 4; [ReCp(O)3], pseudo-octahedral, [ReL2X7], 18, 0, 7, 6; 2– 2– [PtCl4] , square planar, [PtX4] , 16, 8, 2, 4; – – [PtCl3(C2H4)] , square planar, [PtLX3] , 16, 8, 2, 4; [CoCp2], sandwich structure with parallel rings, [CoL4X2], 19, 7, 2, 6; 6 [Fe( -C6Me6)2], sandwich structure with parallel rings, [FeL6], 20, 8, 0, 6; [AuCl(PPh3)], linear, [AuLX], 14, 10, 1, 2; 4 [Fe( -C8H8)(CO)3], trigonal bipyramid (piano stool), [FeL5], 18, 8, 0, 5; 1 2+ 2+ [Ru(NH3)5( -C5H5N)] , octahedral, [RuL6] , 18, 6, 2, 6; 2 + + [Re(CO)4( -phen)] , octahedral, [(ReL6] , 18, 6, 1, 6; + + [FeCp*(CO)(PPh3)(CH2)] , pseudo-octahedral (piano stool), [(FeL4X3] , 18, 6, 4, 6; 2+ 2+ [Ru(bpy)3] , pseudo-octahedral, [RuL6] , 18, 6, 2, 6. 2 1.2. In the form [FeCp*( -dtc)2], both dithiocarbamate ligands are chelated to iron, 2 1 [FeL4X3], 19, 5, 3, 7.
    [Show full text]
  • Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
    International Union of Pure and Applied Chemistry Nomenclature of Inorganic Chemistry IUPAC RECOMMENDATIONS 2005 Issued by the Division of Chemical Nomenclature and Structure Representation in collaboration with the Division of Inorganic Chemistry Prepared for publication by Neil G. Connelly Ture Damhus University of Bristol, UK Novozymes A/S, Denmark Richard M. Hartshorn Alan T. Hutton University of Canterbury, NewZealand University of Cape Town, South Africa IR-9.3 COORDINATION COMPOUNDS IR-9.3.2.2 Choosing between closely related geometries For real molecules or ions, the stereochemical descriptor should be based on the nearest idealizedgeometry. However, someidealized geometries are closely related [ e.g. square planar ( SP-4), four-coordinate square pyramidal ( SPY- 4), see-saw ( SS-4), and tetrahedral ( T-4);T-shaped ( TS- 3), trigonalplanar ( TP-3), and trigonalpyramidal ( TPY-3)] and care may therefore be requiredinmaking the choice. The following approach is useful in determining the polyhedralsymbol for four- coordinate structures. The key is to consider the locations of the central atom and the coordinating atoms in relation to each other. If all five atoms are in (or are close to beingin) the same plane, then the molecule should be treated as square planar. If the four coordinating atoms are in aplane, but the central atom is significantly displaced from the plane, then the squarepyramidal geometry is appropriate.Ifthe four coordinating atoms do not lie in (or close to) aplane, then apolyhedron can be defined by joiningall four coordinating atoms togetherwith lines. If the central atom lies inside this polyhedronthe molecule shouldberegarded as tetrahedral, otherwise, it should be regarded as having a see-saw structure.
    [Show full text]
  • Organometallic Chemistry of Some Manganese and Zirconium Complexes: a Green Chemistry Approach
    ORGANOMETALLIC CHEMISTRY OF SOME MANGANESE AND ZIRCONIUM COMPLEXES: A GREEN CHEMISTRY APPROACH S S MANZINI ORGANOMETALLIC CHEMISTRY OF SOME MANGANESE AND ZIRCONIUM COMPLEXES: A GREEN CHEMISTRY APPROACH Sunnyboy Stanley Manzini A thesis submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfillment of the requirements for the degree of Doctor of Philosophy Johannesburg, 2005 DECLARATION I declare that this thesis is my own, unaided work, performed under the supervision of Professor N. J. Coville and Dr W. Meyer. It is submitted for the Degree of Doctor of Philosophy in the University of Witwatersrand, Johannesburg, South Africa. It has not been submitted before for any degree or examination in any other University. Sunnyboy Stanley Manzini September 2005 ii ABSTRACT The solventless reaction between Mn(CO)4(PPh3)Br and PPh3 as neat reagents using FTIRS was conducted and the activation enthalpy change of formation was found to be 143 ± 19 kJmol-1 while the activation entropy change of formation was 104 ± 7 Jmol-1K-1. The same reaction was also carried out in chloroform and the activation enthalpy change of formation was found to be 146 ± 8 kJmol-1 while the activation entropy change of formation was 114 ± 6 Jmol-1K-1. When the reaction was conducted in TCE solution, the activation enthalpy and entropy changes of formation were 137 ± 6 kJmol-1 and 97 ± 5 Jmol-1K-1 respectively. The solventless reaction of Mn(CO)4(PPh3)Br with PPh3 in KBr matrix using DRIFTS was also conducted and the activation enthalpy change of formation was found to be 169 ± 28 kJ.mol-1 while the activation entropy change of formation was 204 ± 57 J.mol-1.K-1.
    [Show full text]
  • Annotated List of Chemistry Laboratory Experiments with Computer Access
    DOCUMENT RESUME ED 232 855 SE 042 628 AUTHOR Bunce, S. C.; And Others TITLE Annotated List of Chemistry Laboratory Experiments with Computer Access. Final Report. INSTITUTION Rensselaer Polytechnic Inst., Troy, N.Y. SPONS AGENCY National Science Foundation, Washington, D.C. REPORT NO NSF/SED-82030 PUB DATE [82] GRANT 5ED79-23685 NOTE 378p. PUB TYPE Reference Materials - Bibliographies (131) -- Reports - Descriptive(141) EDRS PRICE MF01/PC16 Plus Postage. DESCRIPTORS Biochemistry; *Chemical Analysis; Chemical Reactions; *Chemistry; *College Science; *Databases; Demonstrations (Educational); Higher Education; Information Retrieval; Inorganic Chemistry; *Laboratory Procedures; Organic Chemistry; Science Education; Science Equipment; *Science Experiments IDENTIFIERS National Science Foundation; Physical Chemistry; Polymer Chemistry; Radiochemistry ABSTRACT Project Chemlab was designed to prepare an "Annotated List of Laboratory Experiments in Chemistry from theJournal of Chemical Education (1957-1979)" and to develop a computerfile and program to search for specific types ofexperiments. Provided in this document are listings (photoreduced copies ofprintouts) of over 1500 entries classified into seven major fields ofchemistry and arranged alphabetically by author within each field. Thesefields include; analytical chemistry, biochemistry, inorganic chemistry,physical chemistry, polymer chemistry, and radiochemistry. Eachentry contains a field code, a keyword code(to facilitate visual scanning of the lists and for use in searching the computer
    [Show full text]
  • Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
    NOMENCLATURE OF INORGANIC CHEMISTRY IUPAC Recommendations 2005 IUPAC Periodic Table of the Elements 118 1 2 21314151617 H He 3 4 5 6 7 8 9 10 Li Be B C N O F Ne 11 12 13 14 15 16 17 18 3456 78910 11 12 Na Mg Al Si P S Cl Ar 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe 55 56 * 57− 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 Cs Ba lanthanoids Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn 87 88 ‡ 89− 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 Fr Ra actinoids Rf Db Sg Bh Hs Mt Ds Rg Uub Uut Uuq Uup Uuh Uus Uuo * 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu ‡ 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr International Union of Pure and Applied Chemistry Nomenclature of Inorganic Chemistry IUPAC RECOMMENDATIONS 2005 Issued by the Division of Chemical Nomenclature and Structure Representation in collaboration with the Division of Inorganic Chemistry Prepared for publication by Neil G.
    [Show full text]