Big Chemical Encyclopedia

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

Articles Figures Tables About

Synthetic separators

During the first trials with synthetic separators around 1940 it had already been observed that some of the desired battery characteristics were affected detrimentally. The cold crank performance decreased and there was a tendency towards increased sulfation and thus shorter battery life. In extended test series, these effects could be traced back to the complete lack of wooden lignin, which had leached from the wooden veneer and interacted with the crystallization process at the negative electrode. By a dedicated addition of lignin sulfonates — so called organic expanders -— to the negative mass, not only were these disadvantages removed, but an improvement in performance was even achieved. [Pg.252]

The first synthetic separator is still in use today in some geographical areas, for two reasons this separator is unchallenged in its low raw-material and production costs... [Pg.263]

Presented here are the synthesis and resolution of asym-cis- and sym-cis-[Co(edda)(en)], as well as the synthesis of Na[Co(edda)(C03)] (primarily the asym-cis-isomer) employed for the synthesis of ax>w-c/x-[Co(edda)(en)]Cl. For the preparation of asym-cis complexes there is no advantage in obtaining pure asym-cis- [Co(edda)(C03)]", since some isomerization occurs during the displacement of the carbonate, necessitating subsequent separation of isomers. However, the two isomers of [Co(edda)(C03)] can be obtained readily by fractional crystallization. These synthetic, separation, and resolution procedures are generally useful for charged complexes, such as those of amino acids. [Pg.103]

Synthetic separation membranes are either nonporous or porous. For nonpor-ous membranes, permeability and selectivity are based on a solution-diffusion mechanism examples for technical membrane separations are gas separation, reverse osmosis, or pervaporation. For porous membranes, either diffusive or convective How can yield a selectivity based on size, for larger pore sizes typically according to a sieving mechanism examples for technical membrane separations are dialysis, ultrafiltration, or microfiltration. It is important to note that additional interactions between permeand and membrane, e.g., based on ion exchange or affinity, can change the membrane s selectivity completely membrane adsorbers with a pore structure of a microfiltration membrane are an example. [Pg.456]

A unique feature of the cathode design is the extension of the cathode fingers from the back plate, which allows easy inspection of the cathode surfaces, and the adaptability to use synthetic separators with minor modifications. The anolyte compartment is connected to an independent brine feed tank by flanged connections and chlorine leaves from the top, through the brine feed tank and then to the chlorine header. Each electrolyzer is fitted with a level alarm, which monitors the level of all the cells in the unit. Figure 5.16 is an isometric cutaway of a Glanor V Type 1144 electrolyzer. [Pg.407]

Academia the basic science involved in the behaviour of chiral compounds. If we seek the state of the art in our discipline, we cannot help but think that rapid and selective chemical distinction between enantiomers, which results in their facile separation, is something beautiful in itself There have been many successful methods developed for the synthetic separation of enantiomers, as we shall see, and these are both de facto interesting and instructive to consider for the design of future examples of such processes. The relationship between kinetic resolution and asymmetric catalysis is strong, and one can inform the design of the other. It is hoped that the diverse examples described in this book stimulate thoughts in the reader of what is possible next. [Pg.1]

Scheme 1.10 The Soai reaction that achieves a form of synthetic separation of enantiomers through selective autocatalysis. Scheme 1.10 The Soai reaction that achieves a form of synthetic separation of enantiomers through selective autocatalysis.
These and other processes are not by any means widespread or generalizable, and they have not yet had an impact on the industrial preparation of enantiopure compounds, but are included as suggestions of where the vibrant and important field of the synthetic separation of enantiomers might go next Some of these methods also remind us of the prototypical synthetic separation of enantiomers that may have played a role in the origin of life. [Pg.9]

It is fair to say that polymerization processes suitable for the synthetic separation of enantiomers are rare, particularly in any preparative sense, which is perhaps surprising as the obvious differences in sizes of polymer versus monomer make the separation process potentially easy. The scarcity of examples may in part be because the interests of the investigators are focused more on the polymers themselves than resolution processes. Nevertheless, there are a handful of examples (such as those above) where it is clear that a polymerization can very effectively select out an enantiomer from a racemic solution, sometimes mediated by the growing polymer itself independently of any additive. Perhaps, more cases will be discovered in the coming years, in line with recent theoretical predictions of ways in which polymerization might be stereoselective [40-42]. [Pg.271]

Sintered PVC Separators The first synthetic separator is still in use... [Pg.307]

The mercuric oxide-zinc cell for miniature applications is usually based on the familiar button construction using a compressed cathode of mercuric oxide and graphite (added for conductivity) in a plated steel can. The cell seal is supported by a cathode sleeve on top of which is placed a synthetic separator and an electrolyte absorbing pad the electrolyte is a solution of potassium hydroxide. The amalgamated zinc anode is added and the cell sealed with a polymeric gasket and a metal top cap. [Pg.90]


See other pages where Synthetic separators is mentioned: [Pg.617]    [Pg.31]    [Pg.30]    [Pg.263]    [Pg.135]    [Pg.50]    [Pg.8]    [Pg.838]    [Pg.31]    [Pg.59]    [Pg.31]    [Pg.723]   
See also in sourсe #XX -- [ Pg.252 , Pg.268 ]




SEARCH



© 2024 chempedia.info