Search results
Results from the WOW.Com Content Network
Column chromatography in chemistry is a chromatography method used to isolate a single chemical compound from a mixture. Chromatography is able to separate substances based on differential absorption of compounds to the adsorbent; compounds move through the column at different rates, allowing them to be separated into fractions.
Chromatography columns of different types are used in both gas and liquid chromatography: Liquid chromatography: Traditional chromatography columns were made of glass. Modern columns are mostly made of borosilicate glass, acrylic glass or stainless steel. To prevent the stationary phase from leaking out of the column interior a polymer ...
The design and operation of a fractionating column depends on the composition of the feed as well as the composition of the desired products. Given a simple, binary component feed, analytical methods such as the McCabe–Thiele method [5] [8] [9] or the Fenske equation [5] can be used. For a multi-component feed, simulation models are used both ...
In liquid chromatography, the mobile phase velocity is taken as the exit velocity, that is, the ratio of the flow rate in ml/second to the cross-sectional area of the ‘column-exit flow path.’ For a packed column, the cross-sectional area of the column exit flow path is usually taken as 0.6 times the cross-sectional area of the column.
The same equation applies in chromatography processes as for the packed bed processes, namely: = In packed column chromatography, the HETP may also be calculated with the Van Deemter equation. In capillary column chromatography HETP is given by the Golay equation.
Here the distillation head and fractionating column are combined in one piece. Differential centrifugation . Fractionation is a separation process in which a certain quantity of a mixture (of gasses, solids, liquids, enzymes , or isotopes , or a suspension ) is divided during a phase transition , into a number of smaller quantities ( fractions ...
Size-exclusion chromatography, also known as molecular sieve chromatography, [1] is a chromatographic method in which molecules in solution are separated by their shape, and in some cases size. [2] It is usually applied to large molecules or macromolecular complexes such as proteins and industrial polymers. [3]
The chiral stationary phase, CSP, can interact differently with two enantiomers, by a process known as chiral recognition. Chiral recognition depends on various interactions such as hydrogen bonding, π-π interaction, dipole stacking, inclusion complexation, steric, hydrophobic and electrostatic interaction, charge-transfer interactions, ionic interactions etc, between the analyte and the CSP ...