User:Eleni N. Kalivas/Notebook/CHEM-571/2013/09/04: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
Line 41: Line 41:


==Group Calibration Data==
==Group Calibration Data==
*Adenosine group calibration curve
[[Image:Adenosine extinction coefficent.png]]
*Inosine group calibration curve
[[Image:Inosine extinction coefficent.png]]
*Standard Deviations
the chart on the left is the standard deviation table of Adenosine, while that on the right is the standard deviation table of the inosine data
[[Image:Adenosine and Inosine st. deviations ZEM.png]]


<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->

Revision as of 13:54, 9 September 2013

Project name <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Overview

Due to time constraints we were not able to run a UV-vis for the inosine spectra. The objective for today includes analyzing yesterdays data in order to check the spectra and calibration curves and make any necessary corrections, and to also do the same for the inosine solutions.

Analysis

After looking over the data from yesterday there were multiple problems that needed correcting. First we noticed that our 0.5M adenosine was the exact same data as the water that was run as a blank. This lead us to believe that the data was saved incorrectly and that some of the dilutions may have just been off. We re-ran the 0.5M adenosine sample and got comparatively valid data. We then noticed that our 1.0M adenosine peaked below the 0.5M which indicated a clear error. Therefore we re-made the 1.0M adenosine and received much better data. Our last observation was that the 3.0M adenosine was too far off when analyzing the calibration curve, so we also re-made the 3.0M adenosine dilution and re-ran it and received much better data.

  • Preparation of stock solution

  • Adenosine Dilutions

  • Absorbance Spectra of Adenosine


  • Calibration Curve of Adenosine data

Inosine

Once the Adenosine samples had been run and the spectra and the calibration curve had been corrected, the inosine samples were now being run. After running all the data the spectra was plotted and the calibration curve was made. Analysis of the calibration curve concluded.

  • Stock Solution

  • Inosine Dilutions

  • Absorbance spectra of Inosine

  • Calibration curve of Inosine data

Group Calibration Data

  • Adenosine group calibration curve

  • Inosine group calibration curve

  • Standard Deviations

the chart on the left is the standard deviation table of Adenosine, while that on the right is the standard deviation table of the inosine data