Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Osmosis reversible reaction

Completion of Esterification. Because the esterification of an alcohol and an organic acid involves a reversible equiUbrium, these reactions usually do not go to completion. Conversions approaching 100% can often be achieved by removing one of the products formed, either the ester or the water, provided the esterification reaction is equiUbrium limited and not rate limited. A variety of distillation methods can be appHed to afford ester and water product removal from the esterification reaction (see Distillation). Other methods such as reactive extraction and reverse osmosis can be used to remove the esterification products to maximize the reaction conversion (38). In general, esterifications are divided into three broad classes, depending on the volatility of the esters ... [Pg.376]

Quentin may have been the first to sulfonate (arylene ether sulfone).168 In this patent, it was demonstrated that the bisphenol A polysulfone could be sulfonated by chlorosulfonic acid to produce a sulfonated polyfarylene ether sulfone), which was used for desalination via reverse osmosis. However, the chlorosulfonic acid may be capable of cleaving the bisphenol A polysulfone partially at the iso-propylidene link or it might induce branching and crosslinking reactions by... [Pg.351]

In 1977, Parshall and co-workers published their work on the separation of various homogeneous catalysts from reaction mixtures.[46] Homemade polyimide membranes, formed from a solution of polyamic acid were used. After reaction the mixture was subjected to reverse osmosis. Depending on the metal complex and the applied pressure, the permeate contained 4-40% of the original amount of metal. This publication was the beginning of research on unmodified or non-dendritic catalysts separated by commercial and homemade membranes. [Pg.95]

This membrane demonstrated a vastly improved flux compared with the poly(piperazine isophthalamide) membrane, but its seawater salt rejection was low — in the range of 60 to 70 percent. A reverse osmosis test with a magnesium sulfate feedwater showed greater than 99 percent salt retention, however, dispelling the possibility that low sodium chloride rejections were due to defects in the polyamide barrier layer. The piperazine polyamide was soon concluded to have the following structure (see Reaction 111). [Pg.311]

The same nanofiltration experiments were performed with a 50-A ultrafiltration membrane (available from US Filter/Membralox, Warrendale, PA,USA), this time with a monodentate phosphite ligand (24) used for comparison and toluene as the solvent (Table V). Both higher retentions and flux rates for the dendrimers were obtained relative to what was observed with the reverse osmosis membranes. Dendrophite G4 was used in three subsequent reactions carried out with this procedure. [Pg.98]

They fabricated another two kinds of composite membranes through the interfacial reaction of triethylenetetramine 106,107). The one was the (3,(3 -dichloroethylether-triethylenetetramine-isophthaloyl chloride-trimesoyl chloride copolymer membrane, which had the water permeation rate of 2400 1/m2 day and desalination rate of 96.8 %. The other was the adipic-triethylenetetramine-isophthaloyl chloride copolymer membrane, which showed the water flux 95.8 1/m2 day and NaCl rejection 99.8 % on the reverse osmosis of a 0.5% aqueous solution at 25 °C and 42.5 kg/cm2. These characteristics for both membranes did not decrease during the continuous operation for 100 500 hr. [Pg.88]

The chemistry and properties of some of the important interfacial composite membranes developed over the past 25 years are summarized in Table 5.1 [10,12,29,30], The chemistry of the FT-30 membrane, which has an all-aromatic structure based on the reaction of phenylene diamine and trimesoyl chloride, is widely used. This chemistry, first developed by Cadotte [9] and shown in Figure 5.9, is now used in modified form by all the major reverse osmosis membrane producers. [Pg.202]


See other pages where Osmosis reversible reaction is mentioned: [Pg.34]    [Pg.669]    [Pg.714]    [Pg.295]    [Pg.372]    [Pg.790]    [Pg.76]    [Pg.16]    [Pg.32]    [Pg.97]    [Pg.97]    [Pg.201]    [Pg.920]    [Pg.582]    [Pg.1635]    [Pg.1837]    [Pg.2340]    [Pg.118]    [Pg.192]    [Pg.391]    [Pg.242]    [Pg.19]   


SEARCH



Osmosis

Osmosis reversed

Reaction reverse

Reaction reversible

Reactions, reversing

Reverse osmosis

Reversibility Reversible reactions

© 2024 chempedia.info