## Abstract The biologically active pricipals in nature are frequently present as only a few parts per million of complex mixtures of nonβvolatile components and often have limited stability. Their isolation often requires the application of all available techniques, such as adsorption chromatograp
Computer aided experimentation in countercurrent reaction chromatography and simulated countercurrent chromatography
β Scribed by Barry B. Fish; Robert W. Carr; Rutherford Aris
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 725 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0009-2509
No coin nor oath required. For personal study only.
β¦ Synopsis
A continuous countercurrent moving bed chromatographic reactor, and a simulated countercurrent moving bed apparatus have been interfaced with a laboratory microcomputer for data acquisition and computer control. Simulation of a countercurrent moving bed is accomplished by switching a feedstream sequentially through a series of columns. Continuous motion of the bed past the feed, which characterizes true counter-currency, is replaced by discretiaed motion of the feed past the bed. Experimental characterization of the detailed behavior of these configurations requires many analyses of product streams to be done rapidly, virtually mandating computerization. Interfacing of the apparatus with an IB?I PC-XT is described. Representative experimental data from both types of apparatus are presented and briefly discussed.
π SIMILAR VOLUMES
The experimental results of separation of binary volatile mixtures in a 25 mm column have been compared with the results of a multi-stage computation procedure based on established phaseequilibrium data. Very approximate agreement between experiment and theory is obtained assuming an HETP of 13-18 m
The enantiomers of 7-des-methyl-ormeloxifene were separated by countercurrent chromatography (CCC) using sulfated β€-cyclodextrin as chiral selector, representing the first reported successful application of a cyclodextrin derivative in CCCbased resolutions. The choice of chiral selector relies on ex
Three new Annonaceous acetogenins, (2,4-cis and trans)-9-hydroxy asimicinone (1), (2,4-cis and trans)squamoxinone B (2) and (2,4-cis and trans) squamoxinone C (3), were isolated from the bark of Annona squamosa with the help of countercurrent chromatography. Additionally found was isoannoreticuin (4
## Abstract Platycosides, the saponins found in the roots of __Platycodon grandiflorum__ (Platycodi Radix), are typically composed of oleanane triterpenes with two side chains. In platycosides, platycodin D, a glucose unit at Cβ3, is a major component, which has several pharmacological activities.