Process for separating mixture with measurement of purity or yield on intermediate tank
A technology for mixtures and purity, applied in the field of chromatography for separating mixtures, which can solve problems such as hindering measurement and complex analysis equipment.
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[0398] The following examples illustrate the invention without limiting it.
[0399] In subsequent embodiments 1 to 5, the chromatographic simulation model is used, and its parameters are as follows:
[0400] - Substances present in the mixture to be separated: dextran, glucose and fructose with a degree of polymerization (order) greater than or equal to 2;
[0401] - stationary phase: resin XA2004 / 30Ca from Novasep;
[0402] - mobile phase: water;
[0403] - Elution temperature: between 55°C and 65°C.
[0404] These concentration plots representing loading pulses, high concentration saturation, and low concentration saturation at a flow rate of 20 mL / min in a column 2 m long and 8.5 cm in diameter are shown in Figure 5.A , 5.B and 5.C. These data make it possible to use, for example, in the handbook "Preparative Chromatography of Fine Chemicals and Pharmaceutical Agents (Preparative Chromatography of Fine Chemicals and Pharmaceutical Agents)", Henner Schmidt-Traub, Wile...
Embodiment 3
[0406] The method used in Example 3 was SMB with a total column height of 8 meters.
[0407] In the following examples 6 to 7, real chromatographic separations were carried out on a pilot plant using the following parameters:
[0408] - Substances present in the mixture to be separated: dextran, glucose and fructose with a degree of polymerization greater than or equal to 2;
[0409] - stationary phase: resin XA2004 / 30Ca from Novasep;
[0410] - mobile phase: water;
[0411] - Elution temperature: between 55°C and 65°C;
[0412] - The pilot plant consists of 4 chromatographic columns with a length of 2 meters and a diameter of 8.5 centimeters;
[0413] - The flow rate of product and eluent is between 20 and 30 mL / min;
[0414] - The method used is SSMB with a total column height of 8 meters.
Embodiment 1
[0416] A simulation of the chromatographic method was performed as described above.
[0417] Stabilize the system between cycles 1 and 10, fixing and keeping the volumes of the different regions constant. The volume of mobile phase injected was 0.18 BV (bed volume).
[0418] Starting from the 10th cycle, use +0.17 (deviation of the target position from the characteristic point of the adsorption volume divided by the cycle volume, relative to the average eluent injection position) located in the region 4 and -0.17 in the region 1 (the target position and The deviation of the characteristic point of the desorption volume divided by the cycle volume, relative to the target position of the characteristic point of the average eluent injection position) to adjust the area. This corresponds to the target position of the low concentration feature point at the mean eluent injection point.
[0419] Then, without limiting the volume of the mobile phase, the method using two characteris...
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