User:Allison K. Alix/Notebook/CHEM-581/2013/02/13: Difference between revisions

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* Add data and results here...
* See observations for deviations from this procedure.


==Observations==
==Observations==

Revision as of 09:00, 13 February 2013

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Objective

  • Wash nanogels prepared on 02/06/13 with 500mL of acetone.
  • Filter and separate nanogels to be used in later studies (dye attachement, liposome attachment, swelling)
  • Measure the mass of hydrogels that were placed in water on 02/08/13

Description

Nanogels are currently in mineral oil that they were originally prepared in. Acetone will be used to separate the nanogels from the oil from which tey will then be able to be filtered out of and dried.

Procedures

1) Add mineral oil/PVOH emulsion to separatory funnel. Add ~500mL of acetone and shake thoroughly, being careful to release any pressure that has built up.

2) Vacuum filter acetone and dry hydrogels. Store at 4°C


  • See observations for deviations from this procedure.

Observations

When acetone and mineral oil were placed in the separatory funnel, it was immediately noticed that mineral oil was insoluble in acetone. The original procedure which these methods were adapted from used silicone oil in place of mineral oil, which is slightly soluble in acetone. To accommodate for this, ~400mL H2O was then added to the mixture which the nanogels were then re-suspended in. They were rather concentrated and ended up adsorbing to one another so that there were several large aggregates. These aggregates were further broken apart using sonication. Although not completely detached from one another, the mixture was then vacuum filtrated. Upon removal from the vacuum filtration, it was evident that there was still water present in the nanogels. To completely remove this water and promote solid formation, they were lyopholized for 1 day.