Green chemistry

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This article is about the concept of the environmentally friendly design of chemical products and processes. For the journal, see Green Chemistry (journal).

Green chemistry, also called sustainable chemistry, is an area of chemistry and chemical engineering focused on the designing of products and processes that minimize the use and generation of hazardous substances.[1] Whereas environmental chemistry focuses on the effects of polluting chemicals on nature, green chemistry focuses on the environmental impact of chemistry, including technological approaches to preventing pollution and reducing consumption of nonrenewable resources.[2][3][4][5][6][7]

The overarching goals of green chemistry—namely, more resource-efficient and inherently safer design of molecules, materials, products, and processes—can be pursued in a wide range of contexts.

IUPAC definition
Green chemistry (sustainable chemistry): Design of chemical products and processes that reduce or eliminate the use or generation of substances hazardous to humans, animals, plants, and the environment.

Note 1: Modified from ref.[8] to be more general.

Note 2: Green chemistry discusses the engineering concept of pollution prevention and zero waste both at laboratory and industrial scales. It encourages the use of economical and

ecocompatible techniques that not only improve the yield but also bring down the cost of disposal of wastes at the end of a chemical process.[9]

History[edit]

Green chemistry emerged from a variety of existing ideas and research efforts (such as atom economy and catalysis) in the period leading up to the 1990s, in the context of increasing attention to problems of chemical pollution and resource depletion. The development of green chemistry in Europe and the United States was linked to a shift in environmental problem-solving strategies: a movement from command and control regulation and mandated reduction of industrial emissions at the "end of the pipe," toward the active prevention of pollution through the innovative design of production technologies themselves. The set of concepts now recognized as green chemistry coalesced in the mid- to late-1990s, along with broader adoption of the term (which prevailed over competing terms such as "clean" and "sustainable" chemistry).[10][11]

In the United States, the Environmental Protection Agency played a significant early role in fostering green chemistry through its pollution prevention programs, funding, and professional coordination. At the same time in the United Kingdom, researchers at the University of York contributed to the establishment of the Green Chemistry Network within the Royal Society of Chemistry, and the launch of the journal Green Chemistry.[11]

Principles[edit]

In 1998, Paul Anastas (who then directed the Green Chemistry Program at the US EPA) and John C. Warner (then of Polaroid Corporation) published a set of principles to guide the practice of green chemistry.[12] The twelve principles address a range of ways to reduce the environmental and health impacts of chemical production, and also indicate research priorities for the development of green chemistry technologies.

The principles cover such concepts as:

The twelve principles of green chemistry are:[13]

  1. Prevention. Preventing waste is better than treating or cleaning up waste after it is created.
  2. Atom economy. Synthetic methods should try to maximize the incorporation of all materials used in the process into the final product.
  3. Less hazardous chemical syntheses. Synthetic methods should avoid using or generating substances toxic to humans and/or the environment.
  4. Designing safer chemicals. Chemical products should be designed to achieve their desired function while being as non-toxic as possible.
  5. Safer solvents and auxiliaries. Auxiliary substances should be avoided wherever possible, and as non-hazardous as possible when they must be used.
  6. Design for energy efficiency. Energy requirements should be minimized, and processes should be conducted at ambient temperature and pressure whenever possible.
  7. Use of renewable feedstocks. Whenever it is practical to do so, renewable feedstocks or raw materials are preferable to non-renewable ones.
  8. Reduce derivatives. Unnecessary generation of derivatives—such as the use of protecting groups—should be minimized or avoided if possible; such steps require additional reagents and may generate additional waste.
  9. Catalysis. Catalytic reagents that can be used in small quantities to repeat a reaction are superior to stoichiometric reagents (ones that are consumed in a reaction).
  10. Design for degradation. Chemical products should be designed so that they do not pollute the environment; when their function is complete, they should break down into non-harmful products.
  11. Real-time analysis for pollution prevention. Analytical methodologies need to be further developed to permit real-time, in-process monitoring and control before hazardous substances form.
  12. Inherently safer chemistry for accident prevention. Whenever possible, the substances in a process, and the forms of those substances, should be chosen to minimize risks such as explosions, fires, and accidental releases.

Trends[edit]

Attempts are being made not only to quantify the greenness of a chemical process but also to factor in other variables such as chemical yield, the price of reaction components, safety in handling chemicals, hardware demands, energy profile and ease of product workup and purification. In one quantitative study,[14] the reduction of nitrobenzene to aniline receives 64 points out of 100 marking it as an acceptable synthesis overall whereas a synthesis of an amide using HMDS is only described as adequate with a combined 32 points.

Green chemistry is increasingly seen as a powerful tool that researchers must use to evaluate the environmental impact of nanotechnology.[15] As nanomaterials are developed, the environmental and human health impacts of both the products themselves and the processes to make them must be considered to ensure their long-term economic viability.[citation needed]

Examples[edit]

Green solvents[edit]

Solvents are consumed in large quantities in many chemical syntheses as well as for cleaning and degreasing. Traditional solvents are often toxic or are chlorinated. Green solvents, on the other hand, are generally derived from renewable resources and biodegrade to innocuous, often a naturally occurring product.[16][17]

Synthetic techniques[edit]

Novel or enhanced synthetic techniques can often provide improved environmental performance or enable better adherence to the principles of green chemistry. For example, the 2005 Nobel Prize for Chemistry was awarded, to Yves Chauvin, Robert H. Grubbs and Richard R. Schrock, for the development of the metathesis method in organic synthesis, with explicit reference to its contribution to green chemistry and "smarter production."[18] A 2005 review identified three key developments in green chemistry in the field of organic synthesis: use of supercritical carbon dioxide as green solvent, aqueous hydrogen peroxide for clean oxidations and the use of hydrogen in asymmetric synthesis.[19] Some further examples of applied green chemistry are supercritical water oxidation, on water reactions, and dry media reactions.[citation needed]

Bioengineering is also seen as a promising technique for achieving green chemistry goals. A number of important process chemicals can be synthesized in engineered organisms, such as shikimate, a Tamiflu precursor which is fermented by Roche in bacteria. Click chemistry is often cited[citation needed] as a style of chemical synthesis that is consistent with the goals of green chemistry. The concept of 'green pharmacy' has recently been articulated based on similar principles.[20]

Carbon dioxide as blowing agent[edit]

In 1996, Dow Chemical won the 1996 Greener Reaction Conditions award for their 100% carbon dioxide blowing agent for polystyrene foam production. Polystyrene foam is a common material used in packing and food transportation. Seven hundred million pounds are produced each year in the United States alone. Traditionally, CFC and other ozone-depleting chemicals were used in the production process of the foam sheets, presenting a serious environmental hazard. Flammable, explosive, and, in some cases toxic hydrocarbons have also been used as CFC replacements, but they present their own problems. Dow Chemical discovered that supercritical carbon dioxide works equally as well as a blowing agent, without the need for hazardous substances, allowing the polystyrene to be more easily recycled. The CO2 used in the process is reused from other industries, so the net carbon released from the process is zero.

Hydrazine[edit]

Addressing principle #2 is the Peroxide Process for producing hydrazine without cogenerating salt. Hydrazine is traditionally produced by the Olin Raschig process from sodium hypochlorite (the active ingredient in many bleaches) and ammonia. The net reaction produces one equivalent of sodium chloride for every equivalent of the targeted product hydrazine:[21]

NaOCl + 2 NH3 → H2N-NH2 + NaCl + H2O

In the greener Peroxide process hydrogen peroxide is employed as the oxidant and the side product is water. The net conversion follows:

2 NH3 + H2O2 → H2N-NH2 + 2 H2O

Addressing principle #4, this process does not require auxiliary extracting solvents. Methyl ethyl ketone is used as a carrier for the hydrazine, the intermediate ketazine phase separates from the reaction mixture, facilitating workup without the need of an extracting solvent.

1,3-Propanediol[edit]

Addressing principle #7 is a green route to 1,3-propanediol, which is traditionally generated from petrochemical precursors. It can be produced from renewable precursors via the bioseparation of 1,3-propanediol using a genetically modified strain of E. coli.[22] This diol is used to make new polyesters for the manufacture of carpets.

Lactide[edit]

Lactide

In 2002, Cargill Dow (now NatureWorks) won the Greener Reaction Conditions Award for their improved method for polymerization of polylactic acid . Unfortunately, lactide-base polymers do not perform well and the project was discontinued by Dow soon after the award. Lactic acid is produced by fermenting corn and converted to lactide, the cyclic dimer ester of lactic acid using an efficient, tin-catalyzed cyclization. The L,L-lactide enantiomer is isolated by distillation and polymerized in the melt to make a crystallizable polymer, which has some applications including textiles and apparel, cutlery, and food packaging. Wal-Mart has announced that it is using/will use PLA for its produce packaging. The NatureWorks PLA process substitutes renewable materials for petroleum feedstocks, doesn't require the use of hazardous organic solvents typical in other PLA processes, and results in a high-quality polymer that is recyclable and compostable.

Carpet tile backings[edit]

In 2003 Shaw Industries selected a combination of polyolefin resins as the base polymer of choice for EcoWorx due to the low toxicity of its feedstocks, superior adhesion properties, dimensional stability, and its ability to be recycled. The EcoWorx compound also had to be designed to be compatible with nylon carpet fiber. Although EcoWorx may be recovered from any fiber type, nylon-6 provides a significant advantage. Polyolefins are compatible with known nylon-6 depolymerization methods. PVC interferes with those processes. Nylon-6 chemistry is well-known and not addressed in first-generation production. From its inception, EcoWorx met all of the design criteria necessary to satisfy the needs of the marketplace from a performance, health, and environmental standpoint. Research indicated that separation of the fiber and backing through elutriation, grinding, and air separation proved to be the best way to recover the face and backing components, but an infrastructure for returning postconsumer EcoWorx to the elutriation process was necessary. Research also indicated that the postconsumer carpet tile had a positive economic value at the end of its useful life. EcoWorx is recognized by MBDC as a certified cradle-to-cradle design.

Trans and cis fatty acids

Transesterification of fats[edit]

In 2005, Archer Daniels Midland (ADM) and Novozymes won the Greener Synthetic Pathways Award for their enzyme interesterification process. In response to the U.S. Food and Drug Administration (FDA) mandated labeling of trans-fats on nutritional information by January 1, 2006, Novozymes and ADM worked together to develop a clean, enzymatic process for the interesterification of oils and fats by interchanging saturated and unsaturated fatty acids. The result is commercially viable products without trans-fats. In addition to the human health benefits of eliminating trans-fats, the process has reduced the use of toxic chemicals and water, prevents vast amounts of byproducts, and reduces the amount of fats and oils wasted.

Bio-succinic acid[edit]

In 2011, the Outstanding Green Chemistry Accomplishments by a Small Business Award went to BioAmber Inc. for integrated production and downstream applications of bio-based succinic acid. Succinic acid is a platform chemical that is an important starting material in the formulations of everyday products. Traditionally, succinic acid is produced from petroleum-based feedstocks. BioAmber has developed process and technology that produces succinic acid from the fermentation of renewable feedstocks at a lower cost and lower energy expenditure than the petroleum equivalent while sequestering CO2 rather than emitting it.[23]

Laboratory chemicals[edit]

Several laboratory chemicals are controversial from the perspective of Green chemistry. The Massachusetts Institute of Technology created a "Green" Alternatives Wizard [2] to help identify alternatives. Ethidium bromide, xylene, mercury, and formaldehyde have been identified as "worst offenders" which have alternatives.[24] Solvents in particular make a large contribution to the environmental impact of chemical manufacturing and there is a growing focus on introducing Greener solvents into the earliest stage of development of these processes: laboratory-scale reaction and purification methods.[25] In the Pharmaceutical Industry, both GSK[26] and Pfizer[27] have published Solvent Selection Guides for their Drug Discovery chemists.

Legislation[edit]

The EU[edit]

In 2007, The EU put into place the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) program, which requires companies to provide data showing that their products are safe. This regulation (1907/2006) ensures not only the assessment of the chemicals' hazards as well as risks during their uses but also includes measures for banning or restricting/authorising uses of specific substances. ECHA, the EU Chemicals Agency in Helsinki, is implementing the regulation whereas the enforcement lies with the EU member states.

United States[edit]

The U.S. law that governs the majority of industrial chemicals (excluding pesticides, foods, and pharmaceuticals) is the Toxic Substances Control Act (TSCA) of 1976. Examining the role of regulatory programs in shaping the development of green chemistry in the United States, analysts have revealed structural flaws and long-standing weaknesses in TSCA; for example, a 2006 report to the California Legislature concludes that TSCA has produced a domestic chemicals market that discounts the hazardous properties of chemicals relative to their function, price, and performance.[28] Scholars have argued that such market conditions represent a key barrier to the scientific, technical, and commercial success of green chemistry in the U.S., and fundamental policy changes are needed to correct these weaknesses.[29]

Passed in 1990, the Pollution Prevention Act helped foster new approaches for dealing with pollution by preventing environmental problems before they happen.

In 2008, the State of California approved two laws aiming to encourage green chemistry, launching the California Green Chemistry Initiative. One of these statutes required California's Department of Toxic Substances Control (DTSC) to develop new regulations to prioritize "chemicals of concern" and promote the substitution of hazardous chemicals with safer alternatives. The resulting regulations took effect in 2013, initiating DTSC's Safer Consumer Products Program.[30]

Education[edit]

Many institutions offer courses[31] and degrees on Green Chemistry. Examples from across the globe are Denmark's Technical University,[32] and several in the US, e.g. at the Universities of Massachusetts-Boston,[33] Michigan,[34] and Oregon.[35] A masters level course in Green Technology, has been introduced by the Institute of Chemical Technology, India. In the UK at the University of York[36] University of Leicester, Department of Chemistry and MRes in Green Chemistry at Imperial College London. In Spain different universities like the Universidad de Jaume I[37] or the Universidad de Navarra,[38] offer Green Chemistry master courses. There are also websites focusing on green chemistry, such as the Michigan Green Chemistry Clearinghouse at www.migreenchemistry.org.
Apart from its Green Chemistry Master courses the Zurich University of Applied Sciences ZHAW presents an exposition and web page "Making chemistry green" for a broader public, illustrating the 12 principles.[39]

Scientific journals specialized in green chemistry[edit]

Contested definition[edit]

There are ambiguities in the definition of green chemistry, and in how it is understood among broader science, policy, and business communities. Even within chemistry, researchers have used the term "green chemistry" to describe a range of work independently of the framework put forward by Anastas and Warner (i.e., the 12 principles).[11] While not all uses of the term are legitimate (see greenwashing), many are, and the authoritative status of any single definition is uncertain. More broadly, the idea of green chemistry can easily be linked (or confused) with related concepts like green engineering, environmental design, or sustainability in general. The complexity and multifaceted nature of green chemistry makes it difficult to devise clear and simple metrics. As a result, "what is green" is often open to debate.[40]

Awards[edit]

Several scientific societies have created awards to encourage research in green chemistry.

  • Australia's Green Chemistry Challenge Awards overseen by The Royal Australian Chemical Institute (RACI).
  • The Canadian Green Chemistry Medal.[41]
  • In Italy, Green Chemistry activities center around an inter-university consortium known as INCA.[42]
  • In Japan, The Green & Sustainable Chemistry Network oversees the GSC awards program.[43]
  • In the United Kingdom, the Green Chemical Technology Awards are given by Crystal Faraday.[44]
  • In the US, the Presidential Green Chemistry Challenge Awards recognize individuals and businesses.[45][46]

See also[edit]

References[edit]

  1. ^ "Green Chemistry". United States Environmental Protection Agency. 2006-06-28. Retrieved 2011-03-23.
  2. ^ Sheldon, R. A.; Arends, I. W. C. E.; Hanefeld, U. (2007). Green Chemistry and Catalysis. doi:10.1002/9783527611003. ISBN 9783527611003.
  3. ^ Clark, J. H.; Luque, R.; Matharu, A. S. (2012). "Green Chemistry, Biofuels, and Biorefinery". Annual Review of Chemical and Biomolecular Engineering. 3: 183–207. doi:10.1146/annurev-chembioeng-062011-081014. PMID 22468603.
  4. ^ Cernansky, R. (2015). "Chemistry: Green refill". Nature. 519 (7543): 379–380. doi:10.1038/nj7543-379a.
  5. ^ Sanderson, K. (2011). "Chemistry: It's not easy being green". Nature. 469 (7328): 18–20. Bibcode:2011Natur.469...18S. doi:10.1038/469018a. PMID 21209638.
  6. ^ Poliakoff, M.; Licence, P. (2007). "Sustainable technology: Green chemistry". Nature. 450 (7171): 810–812. Bibcode:2007Natur.450..810P. doi:10.1038/450810a. PMID 18064000.
  7. ^ Clark, J. H. (1999). "Green chemistry: Challenges and opportunities". Green Chemistry. 1: 1–8. doi:10.1039/A807961G.
  8. ^ A. E. Martel, J. A. Davies, W. W. Olson, M. A. Abraham. (2003). Annu. Rev. Environ. Resour. 28: 401. Missing or empty |title= (help)CS1 maint: Multiple names: authors list (link)
  9. ^ Vert, Michel; Doi, Yoshiharu; Hellwich, Karl-Heinz; Hess, Michael; Hodge, Philip; Kubisa, Przemyslaw; Rinaudo, Marguerite; Schué, François (2012). "Terminology for biorelated polymers and applications (IUPAC Recommendations 2012)" (PDF). Pure and Applied Chemistry. 84 (2): 377–410. doi:10.1351/PAC-REC-10-12-04.
  10. ^ Woodhouse, E. J.; Breyman, S. (2005). "Green chemistry as social movement?". Science, Technology, & Human Values. 30 (2): 199–222. doi:10.1177/0162243904271726.
  11. ^ a b c Linthorst, J. A. (2009). "An overview: Origins and development of green chemistry". Foundations of Chemistry. 12: 55–68. doi:10.1007/s10698-009-9079-4.
  12. ^ Anastas, Paul T.; Warner, John C. (1998). Green chemistry: theory and practice. Oxford [England]; New York: Oxford University Press. ISBN 9780198502340.
  13. ^ "12 Principles of Green Chemistry - American Chemical Society". American Chemical Society. Retrieved 2018-02-16.
  14. ^ Van Aken, K.; Strekowski, L.; Patiny, L. (2006). "EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters". Beilstein Journal of Organic Chemistry. 2 (1): 3. doi:10.1186/1860-5397-2-3. PMC 1409775. PMID 16542013.
  15. ^ Green nanotechnology
  16. ^ Prat, D.; Pardigon, O.; Flemming, H.-W.; Letestu, S.; Ducandas, V.; Isnard, P.; Guntrum, E.; Senac, T.; Ruisseau, S.; Cruciani, P.; Hosek, P., "Sanofi’s Solvent Selection Guide: A Step Toward More Sustainable Processes", Org. Proc. Res. Devel. 2013, 17, 1517-1525. doi:10.1021/op4002565
  17. ^ Sherman, J.; Chin, B.; Huibers, P. D. T.; Garcia-Valls, R.; Hatton, T. A., "Solvent Replacement for Green Processing", Environ. Health Persp. 1998, 106, 253-271. doi:10.2307/3433925
  18. ^ "The Nobel Prize in Chemistry 2005". The Nobel Foundation. Retrieved 2006-08-04.
  19. ^ Noyori, R. (2005). "Pursuing practical elegance in chemical synthesis". Chemical Communications (14): 1807–11. doi:10.1039/B502713F. PMID 15795753.
  20. ^ Baron, M. (2012). "Towards a Greener Pharmacy by More Eco Design" (PDF). Waste and Biomass Valorization. 3 (4): 395–407. doi:10.1007/s12649-012-9146-2.
  21. ^ Jean-Pierre Schirmann, Paul Bourdauducq "Hydrazine" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2002. doi:10.1002/14356007.a13_177.
  22. ^ Kurian, Joseph V. "A New Polymer Platform for the Future – Sorona from Corn Derived 1,3-Propanediol" Journal of Polymers and the Environment, Vol. 13, No. 2 (April 2005).
  23. ^ "2011 Small Business Award". United States Environmental Protection Agency. 2013-03-12.
  24. ^ Coombs A. (2009). Green at the Bench. The Scientist.
  25. ^ Bradley, Jean-Claude; Abraham, Michael H.; Acree, William E.; Lang, Andrew (2015). "Predicting Abraham model solvent coefficients". Chemistry Central Journal. 9: 12. doi:10.1186/s13065-015-0085-4. PMC 4369285. PMID 25798192.
  26. ^ Henderson, R. K.; Jiménez-González, C. N.; Constable, D. J. C.; Alston, S. R.; Inglis, G. G. A.; Fisher, G.; Sherwood, J.; Binks, S. P.; Curzons, A. D. (2011). "Expanding GSK's solvent selection guide – embedding sustainability into solvent selection starting at medicinal chemistry". Green Chemistry. 13 (4): 854. doi:10.1039/c0gc00918k.
  27. ^ Alfonsi, K.; Colberg, J.; Dunn, P. J.; Fevig, T.; Jennings, S.; Johnson, T. A.; Kleine, H. P.; Knight, C.; Nagy, M. A.; Perry, D. A.; Stefaniak, M. (2008). "Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation". Green Chem. 10: 31–36. doi:10.1039/B711717E.
  28. ^ Wilson, M. P.; Chia, D. A.; Ehlers, B. C. (2006). "Green chemistry in California: a framework for leadership in chemicals policy and innovation" (PDF). New Solutions. 16 (4): 365–372. doi:10.2190/9584-1330-1647-136p. PMID 17317635.
  29. ^ Wilson, M. P.; Schwarzman, M. R. (2009). "Toward a new U.S. Chemicals policy: Rebuilding the foundation to advance new science, green chemistry, and environmental health". Environmental Health Perspectives. 117 (8): 1202–9. doi:10.1289/ehp.0800404. PMC 2721862. PMID 19672398.
  30. ^ California Department of Toxic Substances Control. "What is the Safer Consumer Products (SCP) Program?". Retrieved 5 September 2015.
  31. ^ Anastas, P.T., Levy, I.J., Parent, K.E., eds. (2009). Green Chemistry Education: Changing the Course of Chemistry. ACS Symposium Series. 1011. Washington, DC: American Chemical Society. doi:10.1021/bk-2009-1011. ISBN 978-0-8412-7447-1.CS1 maint: Uses editors parameter (link)
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  33. ^ "Chemistry, PhD (Green Track) - University of Massachusetts Boston".
  34. ^ Ecology Center Annual Report (2011). [1].
  35. ^ Greener Education Materials, a database of green chemistry topics. EurekAlert. (2009). Thinking of turning your chemistry green? Consult GEMs. AAAS.
  36. ^ MSc in Green Chemistry & Sustainable Industrial Technology at the Green Chemistry Centre of Excellence based at the University of York
  37. ^ Máster Universitario en Química Sostenible. Universitat Jaume I Archived 2015-02-11 at the Wayback Machine
  38. ^ Máster Universitario en Química Sostenible. Universidad Pública de Navarra Archived 2015-02-11 at the Wayback Machine (UPNA).
  39. ^ "Green Chemistry".
  40. ^ Matus, K. J. M.; Clark, W. C.; Anastas, P. T.; Zimmerman, J. B. (2012). "Barriers to the Implementation of Green Chemistry in the United States" (PDF). Environmental Science & Technology. 46 (20): 10892–10899. Bibcode:2012EnST...4610892M. doi:10.1021/es3021777. PMID 22963612.
  41. ^ "Announcing the 2005 Canadian Green Chemistry Medal". RSC Publishing. Retrieved 2006-08-04.
  42. ^ "Chemistry for the Environment". Interuniversity Consortium. Retrieved 2007-02-15.
  43. ^ "Green & Sustainable Chemistry Network, Japan". Green & Sustainable Chemistry Network. Archived from the original on 2001-05-13. Retrieved 2006-08-04.
  44. ^ "2005 Crystal Faraday Green Chemical Technology Awards". Green Chemistry Network. Archived from the original on 2002-12-17. Retrieved 2006-08-04.
  45. ^ "The Presidential Green Chemistry Awards". United States Environmental Protection Agency. Retrieved 2006-07-31.
  46. ^ "Information about the Presidential Green Chemistry Challenge". 2013-02-13. Retrieved 2014-08-10.


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