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Green Chemistry
Green chemistry is the design of chemical products and processes that reduce or eliminate the use and generation of hazardous substances. Whereas environmental chemistry is the chemistry of the natural environment, and of pollutant chemicals in nature, green chemistry seeks to reduce and prevent pollution at its source. In 1990 the Pollution Prevention Act was passed in the United States. This act helped create a modus operandi for dealing with pollution in an original and innovative way.

Green chemistry is an overarching philosophy of chemistry, rather than a subdiscipline of it. It applies to organic chemistry, inorganic chemistry, biochemistry, analytical chemistry, even physical chemistry. The focus is on minimizing the hazard and maximizing the efficiency of any chemical choice. It is distinct from environmental chemistry which focuses on the chemical phenomena in the environment.

In 2005 Ryoji Noyori identified three key developments in green chemistry: use of supercritical carbon dioxide as green solvent, aqueous hydrogen peroxide for clean oxidations and the use of hydrogen in asymmetric synthesis [1]. Examples of applied green chemistry are supercritical water oxidation, on water reactions and dry media reactions.

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.

Paul Anastas, then of the EPA, and John C. Warner developed 12 principles of green chemistry,[2] which help to explain what the definition means in practice. The principles cover such concepts as:

the design of processes to maximise the amount of raw material that ends up in the product;
the use of safe, environment-benign solvents where possible;
the design of energy efficient processes;
the best form of waste disposal, aiming not to create it in the first place.
The 12 principles are:

1.Prevent waste: Design chemical syntheses to prevent waste, leaving no waste to treat or clean up.
2.Design safer chemicals and products: Design chemical products to be fully effective, yet have little or no toxicity.
3.Design less hazardous chemical syntheses: Design syntheses to use and generate substances with little or no toxicity to humans and the environment.
4.Use renewable feedstock: Use raw materials and feedstock that are renewable rather than depleting. Renewable feedstock are often made from agricultural products or are the wastes of other processes; depleting feedstock are made from fossil fuels (petroleum, natural gas, or coal) or are mined.
5.Use catalysts, not stoichiometric reagents: Minimize waste by using catalytic reactions. Catalysts are used in small amounts and can carry out a single reaction many times. They are preferable to stoichiometric reagents, which are used in excess and work only once.
6.Avoid chemical derivatives: Avoid using blocking or protecting groups or any temporary modifications if possible. Derivatives use additional reagents and generate waste.
7.Maximize atom economy: Design syntheses so that the final product contains the maximum proportion of the starting materials. There should be few, if any, wasted atoms.
8.Use safer solvents and reaction conditions: Avoid using solvents, separation agents, or other auxiliary chemicals. If these chemicals are necessary, use innocuous chemicals. If a solvent is necessary, water is usually the best medium.
9.Increase energy efficiency: Run chemical reactions at ambient temperature and pressure whenever possible.
10.Design chemicals and products to degrade after use: Design chemical products to break down to innocuous substances after use so that they do not accumulate in the environment.
11.Analyze in real time to prevent pollution: Include in-process real-time monitoring and control during syntheses to minimize or eliminate the formation of byproducts.
12.Minimize the potential for accidents: Design chemicals and their forms (solid, liquid, or gas) to minimize the potential for chemical accidents including explosions, fires, and releases to the environment.

Presidential Green Chemistry Challenge Awards

The Presidential Green Chemistry Challenge Awards[1] began in 1995 as an effort to recognize individuals and businesses for innovations in green chemistry. Typically five awards are given each year, one in each of five categories: Academic, Small Business, Greener Synthetic Pathways, Greener Reaction Conditions, and Designing Greener Chemicals. Nominations are accepted the prior year, and evaluated by an independent panel of chemists convened by the American Chemical Society. Through 2006, a total of 57 technologies have been recognized for the award, and over 1000 nominations have been submitted.

Glycerine to Propylene Glycol

In 2006, Professor Galen J. Suppes, from the University of Missouri-Columbia, was awarded the Academic Award for his system of converting waste glycerin from biodiesel production to propylene glycol. Through the use of a copper-chromite catalyst, Professor Suppes was able to lower the required temperature of conversion while raising the efficiency of the distillation reaction. Propylene glycol produced in this way will be cheap enough to replace the more toxic ethylene glycol that is the primary ingredient in automobile antifreeze.

Trans and Cis Fatty Acids

In 2005, Archer Daniels Midland (ADM) and Novozymes N.A.[2] won the Greener Synthetic Pathways Award for their enzyme interesterification process. In response to the 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.


In 2002, Cargill Dow (now NatureWorks)[3] won the Greener Reaction Conditions Award for their improved polylactic acid polymerization process. 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 use in many 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.
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.
Other awards
The Royal Australian Chemical Institute (RACI) presents Australia’s Green Chemistry Challenge Awards. This awards program is similar to that at the EPA, although the Institute has included a category for Green Chemistry education as well as Small Business and Academic or Government.

The Canadian Green Chemistry Medal is an annual award given to an individual or group for promotion and development of green chemistry in Canada and internationally. The winner is presented with a citation recognizing the achievements together with a sculpture. [3] [4]

Green Chemistry activities in Italy center around an inter-university consortium known as INCA. Beginning in 1999, the INCA has given three awards annually to industry for applications of green chemistry. The winners receive a plaque at the annual INCA meeting. [5]

In Japan, The Green & Sustainable Chemistry Network(GSCN), formed in 1999, is an organization consisting of representatives from chemical manufacturers and researchers. In 2001, the organization began an awards program. GSC Awards are to be granted to individuals, groups or companies who greatly contributed to green chemistry through their research, development and their industrialization. The achievements are awarded by Ministers of related government agencies. [6]

In the United Kingdom, the Crystal Faraday Partnership, a non-profit group founded in 2001, awards businesses annually for incorporation of green chemistry. The Green Chemical Technology Awards have been given by Crystal Faraday since 2004; the awards were presented by the Royal Society of Chemistry prior to that time. The award is given only to a single researcher or business, while other notable entries are given recognition as well. [7]

The Nobel Prize Committee recognized the importance of green chemistry in 2005 by awarding Yves Chauvin, Robert H. Grubbs, and Richard R. Schrock the Nobel Prize for Chemistry for “the development of the metathesis method in organic synthesis.” The Nobel Prize Committee states, “this represents a great step forward for ‘green chemistry’, reducing potentially hazardous waste through smarter production. Metathesis is an example of how important basic science has been applied for the benefit of man, society and the environment.” [8]

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 [4], 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.

Supramolecular Chemistry

Research is currently ongoing in the area of supramolecular chemistry to develop reactions which can proceed in the solid state without the use of solvents. The cycloaddition of trans-1,2-bis(4-pyridyl)ethylene is directed by resorcinol in the solid state. This solid-state reaction proceeds in the presence of UV light in 100% yield.

Cycloaddition of trans-1,2-bis(4-pyridyl)ethylene

See also
Bioremediation – a technique that generally falls outside the scope of green chemistry
Green computing – a similar initiative in the area of computing

1.^ Pursuing practical elegance in chemical synthesis Ryoji Noyori Chemical Communications, 2005, (14), 1807 – 1811 Abstract
2.^ The 12 Principles of Green Chemistry. U.S. Environmental Protection Agency. Retrieved on 2006-07-31.
3.^ For more information about the Canadian Green Chemistry Medal contact: Professor C. J. Li Coordinator of the Canadian Green Chemistry Network Department of Chemistry, McGill University, 801 Sherbrook St. West, Montreal, Quebec, H3A 2K6, Canada
4.^ EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters. Van Aken K, Strekowski L, Patiny L Beilstein Journal of Organic Chemistry, 2006 2:3 ( 3 March 2006 ) Article

  1. The Presidential Green Chemistry Awards. U.S. Environmental Protection Agency. Retrieved on 2006-07-31.
  2. Novozymes N.A.. Retrieved on 2006-08-04.
    1. NatureWorks LLC. Cargill. Retrieved on 2006-08-01.
    2. Announcing the 2005 Canadian Green Chemistry Medal. RSC Publishing. Retrieved on 2006-08-04.
    3. Chemistry for the Environment. Interuniversity Consortium. Retrieved on 2006-08-04.
    4. Green & Sustainable Chemistry Network, Japan. Green & Sustainable Chemistry Network. Retrieved on 2006-08-04.

11.2005 Crystal Faraday Green Chemical Technology Awards. Green Chemistry Network. Retrieved on 2006-08-04.

12.The Nobel Prize in Chemistry 2005. The Nobel Foundation. Retrieved on 2006-08-04.
13.The MacGillivray Research Group. The MacGillivray Research Group: Research. Retrieved on 2006-05-02.

*Sections taken from From Wikipedia, the free encyclopedia