User:Allison K. Alix/Notebook/CHEM-581/2013/03/01

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(Description)
Current revision (14:17, 1 March 2013) (view source)
(Objective)
 
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==Objective==
==Objective==
Observe hydrogels in solution under microscope
Observe hydrogels in solution under microscope
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Place hydrogels with R6G in solution and observe fluorescence
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Place hydrogels with no R6G in solution with dye to try and get hydrogels to absorb
==Description==
==Description==
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==Procedure==
==Procedure==
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==Data==
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1) Place a small amount of hydrogels (specific mass is arbitrary as we are only trying to see if we can get them to seperate in solution) in ~20mL of water.  
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[[Image:0.5gpva_0.25gl_lecithin_in_safflower_oil.png‎]]
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==Notes==
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2) Vortex to encourage separation
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This area is for any observations or conclusions that you would like to note.
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3) Place a small amount of solution on glass slide (be careful that it is not too concentrated)
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Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.
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==Data==
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[[Image:0.5gpva_0.25gl_lecithin_in_safflower_oil.png‎]]
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[[Category:Course]]
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Hydrogels after being placed in solution
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[[Category:Miscellaneous]]
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==Notes==
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After many attempts, we have concluded that these are indeed our hydrogels that are seen in the above picture. Our next step is to place liposomes around them.

Current revision

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Objective

Observe hydrogels in solution under microscope

Place hydrogels with R6G in solution and observe fluorescence

Place hydrogels with no R6G in solution with dye to try and get hydrogels to absorb

Description

Observation of the hydrogels under a microscope will allow us to see whether or not they are present in solution.

Procedure

1) Place a small amount of hydrogels (specific mass is arbitrary as we are only trying to see if we can get them to seperate in solution) in ~20mL of water.

2) Vortex to encourage separation

3) Place a small amount of solution on glass slide (be careful that it is not too concentrated)

Data

Image:0.5gpva_0.25gl_lecithin_in_safflower_oil.png‎

Hydrogels after being placed in solution

Notes

After many attempts, we have concluded that these are indeed our hydrogels that are seen in the above picture. Our next step is to place liposomes around them.



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