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      The E factor 25 years on: the rise of green chemistry and sustainability

      Green Chemistry
      Royal Society of Chemistry (RSC)

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          Abstract

          The global impact of green chemistry and sustainability and the pivotal role of the E factor concept, over the last twenty five years, is reviewed.

          Abstract

          The global impact, over the last 25 years, of the principles of green chemistry and sustainability, and the pivotal role of the E factor concept in driving resource efficiency and waste minimisation, in the chemical and allied industries, is reviewed. Following an introduction to the origins of green chemistry and the E factor concept, the various metrics for measuring greenness are discussed. It is emphasised that mass-based metrics such as atom economy, E factors and process mass intensity (PMI) need to be supplemented by metrics, in particular life cycle assessment, which measure the environmental impact of waste and, in order to assess sustainability, by metrics which measure economic viability. The role of catalysis in waste minimisation is discussed and illustrated with examples of green catalytic processes such as aerobic oxidations of alcohols, catalytic C–C bond formation and olefin metathesis. Solvent losses are a major source of waste in the pharmaceutical and fine chemical industries and solvent reduction and replacement strategies, including the possible use of neoteric solvents, such as ionic liquids and deep eutectic solvents, are reviewed. Biocatalysis has many benefits in the context of green and sustainable chemistry and this is illustrated with recent examples in the synthesis of active pharmaceutical ingredients. The importance of the transition from an unsustainable economy based on fossil resources to a sustainable bio-based economy is delineated, as part of the overarching transition from an unsustainable linear economy to a truly green and sustainable circular economy based on resource efficiency and waste minimisation by design.

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          Most cited references203

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          Novel solvent properties of choline chloride/urea mixturesElectronic supplementary information (ESI) available: spectroscopic data. See http://www.rsc.org/suppdata/cc/b2/b210714g/

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            Hydroxymethylfurfural, a versatile platform chemical made from renewable resources.

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              Conversion of biomass to selected chemical products.

              This critical review provides a survey illustrated by recent references of different strategies to achieve a sustainable conversion of biomass to bioproducts. Because of the huge number of chemical products that can be potentially manufactured, a selection of starting materials and targeted chemicals has been done. Also, thermochemical conversion processes such as biomass pyrolysis or gasification as well as the synthesis of biofuels were not considered. The synthesis of chemicals by conversion of platform molecules obtained by depolymerisation and fermentation of biopolymers is presently the most widely envisioned approach. Successful catalytic conversion of these building blocks into intermediates, specialties and fine chemicals will be examined. However, the platform molecule value chain is in competition with well-optimised, cost-effective synthesis routes from fossil resources to produce chemicals that have already a market. The literature covering alternative value chains whereby biopolymers are converted in one or few steps to functional materials will be analysed. This approach which does not require the use of isolated, pure chemicals is well adapted to produce high tonnage products, such as paper additives, paints, resins, foams, surfactants, lubricants, and plasticisers. Another objective of the review was to examine critically the green character of conversion processes because using renewables as raw materials does not exempt from abiding by green chemistry principles (368 references).
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                Author and article information

                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2017
                2017
                : 19
                : 1
                : 18-43
                Article
                10.1039/C6GC02157C
                9e68170e-7f5f-433a-a0a6-c781bb78a03f
                © 2017
                History

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