Selectacel®
ION EXCHANCE CELLULOSES
for use in chromatographic columns New Selectacel Ion Exchange Celluloses have remarkable properties when used with ionic and colloidal materials of high molecular weight.
Such applications include —
• ENZYMES · LIPIDS • PROTEINS · NUCLEIC • HORMONES ACIDS
These materials produce separations that far exceed what usually can be accomplished alone by ion exchange resins, chromatography, electro-chromatography, or electrophoresis.
There are several kinds of Selectacel Ion Exchange Celluloses:
A N I O N EXCHANGERS Type DEAE
(Diethyl-aniinoethyl Cellulose)
Grade Standard
20 40
Capacity m e q / g
0.9
Separation and purification of proteins, peptides, enzymes, hormones and related materials.
Type ECTEOLA
(Epichlorohydrin
Grade Standard
20 40
Capacity m e q / g
0.3 triethanolamine)
Separation and purification of viruses.
CATION EXCHANGERS Type CM
~arboxymethyl Cellulose)
Grade Standard
20 40
Capacity m e q / g
0.7
Weakly acidic—most effective at pH's slightly above 4.
Type Ρ
(Cellulose Phosphate)
Grade Standard
Capacity m e q / g
0.9
Bifunctional — containing both strongly acidic and weakly acidic groups. Relatively high exchange capacities.
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CITY STATE Selectacel i s manufactured by Brown Company and exclusively packaged and dis t r ibuted for laboratory use by S & S.
REPORT FOR ANALYTICAL CHEMISTS
The acid is introduced into the container in the molten form and is then allowed to freeze while the container is evacuated. The ampoule is lowered by a clock-work through a bath composed of two immiscible liquids. The liquids are separately maintained at constant temperatures, the ux^per one about 25° C. above the melting point of the acid. Here the acid melts and is brought to a uniform temperature. The lower bath is about 25° C. below the melting point. Very little heat transfer occurs between the two liquids; consequently, there is a rather sharp discontinuity of temperature at the interface between the two liquids. Thus, as the tip of the ampoule passes through the interface, freezing begins and under favorable conditions progresses through the liquid to produce a single crystal. The rate of freezing is about 1 cm. in 24 hours. Although many small crystals form in the tip at first, one or at most two or three will be favored in growth by the zig zag course of crystallization up the tip. Under most favorable conditions, only a single crystal face presents itself at the bottom of the ampoule proper.
This face will be oriented parallel to the plane of temperature discontinuity in the surrounding bath. Impurities other than those, if any such exist, that form a solid solution with benzoic acid, tend to diffuse away from the solid-liquid interface and thus are concentrated in the last portion frozen.
When freezing was complete in the work here described, the ampoule was inverted and the last portion frozen was allowed to melt and flow into one of the collecting bulbs, which was sealed off. The remainder of the acid was then melted and the whole process repeated. The final product was considered to have an over-all purity that would not be distinguishable from ideal purity by any known method. It, therefore, was regarded as a suitable standard for the highly precise acidimétrie measurement to be described later.
Solvent Inclusions in Crysta ls
Potassium biphthalate, likewise sodium oxalate and potassium cli-chromate, are substances which can be purified only by recrystallization from water· solutions, so far as is
Figure 4. Single crystals of ammonium dihydrogen phosphate
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