User:Sarah Haack/Notebook/Capstone Research/2012/02/01: Difference between revisions

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==February 1, 2012==
==February 1, 2012==
* Toady's research included the continuation of last week's UV spectrum analysis. The previous samples, with absorbance rates of 4.00 or higher in the 300-400 nm region. New samples were produced by adding 1 mL of DMF to 2.5 microliters of the most concentrated solution (1 mL DMF with ~2 mg of the substance). These new dilutions were run through the UV spectrometer, and the results were graphed.
* Toady's research included the continuation of last week's UV spectrum analysis. The previous samples, with absorbance rates of 4.00 or higher in the 300-400 nm region. New samples were produced by adding 1 mL of DMF to 2.5 microliters of the most concentrated solution (1 mL DMF with ~2 mg of the substance)in order to produce a solution that was four times more dilute than the original, aiming for absorption closer to 1.00. These new dilutions were run through the UV spectrometer, and the results were graphed.


[[Image:Metal Protoporphyrin Dilute.jpg]]
[[Image:Metal Protoporphyrin Dilute.jpg]]

Revision as of 12:15, 1 February 2012

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February 1, 2012

  • Toady's research included the continuation of last week's UV spectrum analysis. The previous samples, with absorbance rates of 4.00 or higher in the 300-400 nm region. New samples were produced by adding 1 mL of DMF to 2.5 microliters of the most concentrated solution (1 mL DMF with ~2 mg of the substance)in order to produce a solution that was four times more dilute than the original, aiming for absorption closer to 1.00. These new dilutions were run through the UV spectrometer, and the results were graphed.