EugeneOregon
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- Joined
- Jun 12, 2016
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This is dispensary extract that has soaked over night in rubbing alcohol. 70% isopropyl/30% water.
After the extract in rubbing alcohol was pulled through an aluminum oxide column all of the waxes virtually have been removed. Then it was loaded into my horizontal distillation rig which I use only to remove the terpenes. Shown below with terpenes collected in first bulb.
The crude now with terpenes removed is transferred to a cryogenic sublimation apparatus used as a short path device.
Multiple runs through the device increase purity. This shot shows the final pass. Prior to last run I perform a Dry Column Vacuum Chromatography run to remove trace compounds that get generated during initial distillation. Then a final pass in the apparatus seen below collecting Delta 9 isolate on the cold finger. Temperature is 135C nominal set at the heating mantle and pressure is reported by the Pirani based gauge at ¾ of one micron. Atmospheric pressure is typically 760,000 microns and a theoretical perfect vacuum is zero microns. ¾ of one micron is a very deep vacuum. So deep in fact that gas molecules are so scarce that the stop bumping into one another before they hit the glass walls inside. This is called mean free path molecular flow conditions and within it gas molecules can only travel straight lines. All gas that contacts the icy cold finger is deposited and harvested later.
This is Delta 9 THC isolate harvested straight off the cold finger.
All thermal byproducts have been removed with a Chromatography run over standard gel prior to the last pass. Here is a link done on crude to show how the DCVC Chromatography works.
https://future4200.com/t/dcvc-high-column-load-run-on-crude/748
After the extract in rubbing alcohol was pulled through an aluminum oxide column all of the waxes virtually have been removed. Then it was loaded into my horizontal distillation rig which I use only to remove the terpenes. Shown below with terpenes collected in first bulb.
The crude now with terpenes removed is transferred to a cryogenic sublimation apparatus used as a short path device.
Multiple runs through the device increase purity. This shot shows the final pass. Prior to last run I perform a Dry Column Vacuum Chromatography run to remove trace compounds that get generated during initial distillation. Then a final pass in the apparatus seen below collecting Delta 9 isolate on the cold finger. Temperature is 135C nominal set at the heating mantle and pressure is reported by the Pirani based gauge at ¾ of one micron. Atmospheric pressure is typically 760,000 microns and a theoretical perfect vacuum is zero microns. ¾ of one micron is a very deep vacuum. So deep in fact that gas molecules are so scarce that the stop bumping into one another before they hit the glass walls inside. This is called mean free path molecular flow conditions and within it gas molecules can only travel straight lines. All gas that contacts the icy cold finger is deposited and harvested later.
This is Delta 9 THC isolate harvested straight off the cold finger.
All thermal byproducts have been removed with a Chromatography run over standard gel prior to the last pass. Here is a link done on crude to show how the DCVC Chromatography works.
https://future4200.com/t/dcvc-high-column-load-run-on-crude/748
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