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  2. Green solvent - Wikipedia

    en.wikipedia.org/wiki/Green_solvent

    Green solvents are environmentally friendly chemical solvents that are used as a part of green chemistry.They came to prominence in 2015, when the UN defined a new sustainability-focused development plan based on 17 sustainable development goals, recognizing the need for green chemistry and green solvents for a more sustainable future. [1]

  3. Dihydrolevoglucosenone - Wikipedia

    en.wikipedia.org/wiki/Dihydrolevoglucosenone

    Dihydrolevoglucosenone is considered a "green" replacement for DMF. [5] Several standard reactions of organic chemistry, e.g. Menshutkin reaction, [5] Sonogashira coupling, [18] Suzuki-Miyaura coupling [19] and the production of ureas [20] have been carried out in dihydrolevoglucosenone. Formation of ureas using dihydrolevoglucosenone as a solvent

  4. γ-Valerolactone - Wikipedia

    en.wikipedia.org/wiki/Γ-Valerolactone

    Due to the toxicity of the traditional solvents, green solvents were investigated in recent years. [14] Due to its environmentally friendly profile, gamma-valerolactone showed the potential to fabricate polysulfone membranes as a co-solvent.

  5. Green chemistry - Wikipedia

    en.wikipedia.org/wiki/Green_chemistry

    In short, the impact of the entire lifetime of the solvent, from cradle to grave (or cradle to cradle if recycled) must be considered. Thus the most comprehensive definition of a green solvent is the following: "a green solvent is the solvent that makes a product or process have the least environmental impact over its entire life cycle." [23]

  6. Francesca M. Kerton - Wikipedia

    en.wikipedia.org/wiki/Francesca_M._Kerton

    Kerton is the co-author of the book Alternative Solvents for Green Chemistry, which is published by the Royal Society for Chemistry. She has also authored Fuels, Chemicals and Materials from the Oceans and Aquatic Sources, which is published by Wiley.

  7. Talk:Green chemistry - Wikipedia

    en.wikipedia.org/wiki/Talk:Green_chemistry

    Green chemistry in the pharmaceutical industry, Published 2010; Alternative solvents for green chemistry by Kerton, Francesca M. Published 2013; Handbook of green chemistry and technology, Published 2002; Green chemistry and engineering by Doble, Mukesh Published 2007; Green Chemistry for Environmental Remediation, by Sanghi, Rashmi Published 2012

  8. Cyclopentyl methyl ether - Wikipedia

    en.wikipedia.org/wiki/Cyclopentyl_methyl_ether

    Cyclopentyl methyl ether (CPME), also known as methoxycyclopentane, is a hydrophobic ether solvent. A high boiling point of 106 °C (223 °F) and preferable characteristics such as low formation of peroxides, relative stability under acidic and basic conditions, formation of azeotropes with water coupled with a narrow explosion range render CPME an attractive alternative to other ethereal ...

  9. Inorganic nonaqueous solvent - Wikipedia

    en.wikipedia.org/wiki/Inorganic_nonaqueous_solvent

    An inorganic nonaqueous solvent is a solvent other than water, that is not an organic compound. These solvents are used in chemical research and industry for reactions that cannot occur in aqueous solutions or require a special environment. Inorganic nonaqueous solvents can be classified into two groups, protic solvents and aprotic solvents.