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Green Solvent Chemistry

The third level of intention within this volume will be to supply specific, detailed information, and references, so that it will be a basic reference book for green chemistry solvents. This information will be on specific solvents and on discussions of their properties ( why they are appropriate). This information will have indices, so that it may be easily searched. [Pg.19]

The elimination of volatile organic solvents in organic syntheses is a most important goal in green chemistry. Solvent-free organic reactions make syntheses simpler, save energy, and prevent solvent wastes, hazards, and toxicity. [Pg.440]

Another very important green chemistry solvent is supercritical water (SCW) [14], Water under supercritical conditions is an extremely powerful oxidizing and cleansing agent that has been proven remarkably promising as a soil decontaminant by efficiently degrading persistent organic toxic wastes that are difficult to eliminate from polluted soils, and in the treatment of several types of industrial wastes such as textile and cellulose wastewater [2],... [Pg.434]

The chemical stability, negligibly low volatility and easy recycling have placed ionic liquids at the top of green chemistry solvents [33-35]. Figure 6.2 presents the structures of the ionic liquids most frequently used as solvents in organic synthetic chemistry. [Pg.152]

In recent years, much attention has been paid to the environmental impact of industrial processes, and this has promoted increasing efforts toward green chemistry. Solvents play a very important role in the chemical industry. Solvents can influence reaction processes through their effect on solubihties, transport properties, separations, and the reaction rate and selectivity through the solvation effect. Since most of the solvents in current use are derived direcdy or indirectly from petroleum, there are significant drivers to find replacements for conventional solvents to reduce the environmental impact [1]. [Pg.469]

MLC enables to analyse drugs and active phamiaceutical substances without using special column and lai ge quantity of organic solvents. So, from the point of view of pharmaceutical analysis ecology and green chemistry conception, assay with MLC using will be better than conventional reversed-phase chromatography. [Pg.390]

A solventless synthesis of pyrazoles, a green chemistry approach, has been described where an equimolar amount of the diketone and the hydrazine are mixed in a mortar with a drop of sulfuric acid and ground up. After an appropriate length of time ( 1 h) the product is purified to provide clean products. Even acyl pyrazoles 42 were obtained under the solvent-less reaction conditions in good yields. [Pg.296]

Ionic liquids have several important features that make them attractive for use as solvents, particularly in green chemistry ... [Pg.957]

The discussion is organized in the following order First the advantages of HRC scheme, relative to the industrial (i.e., heterogenous) process are briefly commented on second, the relevance of celMose activation and the physical state of its solution to optimization of esterification are discussed. Finally, the use of recently introduced solvent systems and synthetic schemes, designed in order to obtain new, potentially useful cellulose esters with controlled, reproducible properties is reviewed. A comment on the conformity of these methods with the concepts of green chemistry is also included. [Pg.107]

As a cautionary note PTC should not be considered a panacea for all of the problems associated with green chemistry. Two-phase reactions involving water are often difficult to deal with industrially, particularly if the water is contaminated with trace amounts of hazardous organic substances. In some cases it may be more practical, cost effective and environmentally prudent to avoid production of aqueous waste in favour of a recyclable less benign solvent. [Pg.120]

Synthesis of metal carbonyl clusters on oxide surfaces (followed by extraction into a solvent and workup) is occasionally a more convenient and efficient method for preparation of a metal carbonyl cluster than conventional solution chemistry. This synthetic strategy offers the green chemistry advantage of minimizing solvent use, as the reaction often occurs in the absence of solvent. [Pg.214]

Capello, C., Fischer, U., Hungerbuhler, K. (2007) What is a Greeu Solveut A Comprehensive Framework for the Environmental Assessment of Solvents. Green Chemistry, 9(9), 927-934. [Pg.227]


See other pages where Green Solvent Chemistry is mentioned: [Pg.47]    [Pg.205]    [Pg.421]    [Pg.47]    [Pg.205]    [Pg.421]    [Pg.281]    [Pg.376]    [Pg.956]    [Pg.103]    [Pg.113]    [Pg.115]    [Pg.141]    [Pg.317]    [Pg.162]    [Pg.23]    [Pg.137]    [Pg.149]    [Pg.163]    [Pg.244]    [Pg.293]    [Pg.312]    [Pg.729]    [Pg.364]    [Pg.16]    [Pg.1]    [Pg.21]    [Pg.21]    [Pg.22]    [Pg.179]    [Pg.273]    [Pg.273]    [Pg.274]    [Pg.276]    [Pg.298]   
See also in sourсe #XX -- [ Pg.5 ]




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