2021年2月1日星期一

Guide to Flash Chromatography Column (Chapter 2)

 Guide to Flash Chromatography Column (Chapter 2)

4. Determine the appropriate ratio of silica gel to the compound. For simple separation, the ratio of the two is usually 30~50:1 (weight ratio); but for the more difficult separation, the ratio is as high as 120:1.

5. Choose a suitable flash separation column. The amount of silica you need determines the size of the separation column. Whether to use a short and thick or long and thin separation column.

6. Select the appropriate test tube for collection. This is also a good opportunity to consult experienced colleagues. But there is also a simple method: divide the volume of silica gel by 4, and then select a test tube that can hold this volume. (200mL silica gel corresponds to 50mL component).empty flash column chromatography

7. Once you have selected the separation column, you need to block the bottom end of the piston to avoid the loss of silica gel. Usually, it can be done with a small ball of cotton or glass wool plus a long stick or glass rod.

8. Pack the flash separation column in the fume hood. Considering the use of a large number of volatile solvents and the health hazards of dry silica gel, it is not allowed to operate the flash column outside the fume hood. Check to make sure that the flash column is completely vertical. The inclined column is not conducive to separation.

9. Close the piston and add a few inches of eluent.

10. Use the funnel to add some sand (dry and washed) to the flash separation column. The purpose is to spread a thin layer of sand (no more than 1cm) on the plug, so as to prevent silica gel from falling into the collection bottle.

11. Measure the appropriate amount of silica gel. The safest way is to measure it in a fume hood. The density of silica gel is about 0.5 g/mL, so it can be measured directly in an Erlenmeyer flask (100g=200mL). Do not let the volume of silica gel exceed 1/3 of the flask, because we have to add solvent to it.

12. Add at least 1.5 times the volume of solvent to the newly measured silica gel, make it into a slurry, vigorously shake and stir it to make it fully mixed, and remove the gas in the silica gel (the presence of bubbles will make the flash separation column, the efficiency is greatly reduced).

13. Use the powder funnel to carefully and slowly move the slurry into the flash separation column, taking care not to damage the sand layer below. Pay attention to stop and shake the slurry from time to time during the grouting process to ensure that the silica gel is evenly mixed. After grouting, rinse the flask several times with the eluent and add the remaining solvent silica gel mixture to the separation column.

14. Use a dropper and eluent to rinse the silica gel stuck on the top edge of the flash column into the solvent layer.

15. When all the silica gel has been washed away from the flash column wall, open the piston and pressurize the column with compressed air. The silica gel in the column will be compressed to about half of its original height. Check to make sure that the top section of the column is flat. If it is not, it must be stirred again and then settled down. Under pressure, add excess eluent and tap the column gently with a pencil tip or rubber stopper. This will make the silica particles packed more tightly.

Collect all the eluate from the flash column and reuse it after adding the compound.

Note: Remember not to let the solvent level be lower than the filling layer.

Guide to Flash Chromatography Column (Chapter 2)

Calibrating Multichannel Pipettor To Prevent Errors

Calibrating Multichannel Pipettor To Prevent Errors

Widely used in chemistry, molecular biology research, and medical tests in the lab as well, a pipettor is a handy instrument for transporting a measured volume of liquid. It can draw up and dispense liquid by creating a vacuum above the liquid-holding chamber and releasing this vacuum. From single piece glass pipettors to complex adjustable or electronic pipettor, Hawach provides pipettors in several designs for various purposes, and in different levels of accuracy and precision too.

On one hand, a pipettor needs are accurate to the degree with the delivered volume being equal to the specified volume, on the other hand, for precision, it needs to be concerned with the closeness of several measurements to each other. For example, a pipettor might be consistently inaccurate but this inaccuracy could be very precise you still can get the reproducible result out of your samples.

Advanced-Fully-Autoclave-8-12-Channel-Adjustable-Pipettes

The scientists always prefer the perfect pipetting with accuracy and precision for their applications. It is important to work hard to get maxim accuracy and precision and reduce the level of uncertainty at the same time. To reduce the risk of error in manual liquid handling, you need to choose Hawach pipetting system, consisting of the highest quality pipettors professionally maintained and calibrated. And they can be used with the high quality matched tips. With Hawach pipetting products on hands, the correct pipetting angle, speed, and a smooth, consistent pipetting rhythm will help you get better results.

In order to prevent errors when using a multi-channel pipettor, you must learn how to calibrate the main characteristics of the multichannel pipettor:
1. Large-sized central pipetting control button, independent tip removal button.
2. Ergonomically designed finger rest that fits the hand and is easy to hold.
3. Real one-handed operation-regardless of the left or right hand, you can easily set the pipetting volume with one hand.
4. Range lock to prevent unintentional range changes.

Calibration steps for multichannel pipettors
a. Adjust the pipettor to the volume to be calibrated and select the appropriate tip;
b.Adjust the balance;
c. Suck and blow distilled water back and forth 3 times to make the tip wet, wipe the tip with gauze;
d. Hold the pipettor vertically, immerse the tip into the liquid surface 2 ~ 3mm, and slowly (1 ~ 3 seconds) suck the distilled water consistently;
e. Remove the tip from the liquid surface and lean against the tube wall to remove the liquid outside the tip;
f.Put the pipettor into the weighing beaker at an angle of 30 °C. Slowly and uniformly press the pipettor to the first position, wait for 1 to 3 seconds, and then press it to the second position to completely discharge the liquid in the tip;
g. Record the weighing value;
h. Dry the outside of the tip;
i. Weigh 10 times according to the above steps;
j.Take the average value of 10 measurements as the weight of distilled water absorbed by the final pipettor, and calculate the volume according to the Z factor of distilled water listed in Appendix 1;
k. Adjust the pipettor according to the calibration result.
The above is all about sharing how to calibrate in order to prevent mistakes when using multi-channel pipettors today. I hope it will be helpful for everyone to use this device in the future.

Calibrating Multichannel Pipettor To Prevent Errors