User:Michael S. Bible/Notebook/571/2014/10/22: Difference between revisions

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|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span>
|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span>
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***The Ag/AgI wire can be connected directly to a multimeter using alligator clips
***The Ag/AgI wire can be connected directly to a multimeter using alligator clips
***You will continue to connect your Ag wire to the red lead on the multimeter
***You will continue to connect your Ag wire to the red lead on the multimeter
Protocol taken from [[User:Douglas_M._Fox/Notebook/AU_CHEM-571_F2011_Lab_Support/2014/10/21|Dr. Fox]].


Use this iodide ion selective electrode to create a calibration curve for [I<sup>-</sup>].
Use this iodide ion selective electrode to create a calibration curve for [I<sup>-</sup>].


==Description==
==Additional Dialysis Analysis==
# Add experimental record here. Include what, how, and why...
 
Jake did the following:
 
# Ran Titration Analysis on KI-Colloid dialysis
# Ran Bradford Analysis on KI-Colloid dialysis
 
====Description====
# Titration
## Added 3mL 1M HNO<sub>3</sub> and 0.5mL KI solution to 10mL DI H<sub>2</sub>O
## Added 2 mL AgNO<sub>3</sub> and swirl to complete precipitation
## Added 200 μL Ferric alum indicator
## Titrate with your NH<sub>4</sub>SCN solution
# Ran Bradford Analysis on KI-Colloid dialysis
## As expected, the Bradford analysis held a constant protein concentration
##* Lysozyme is too big to pass through the 3500 MWCO so it was constant on one side
##* KI is not expected to react with lysozyme so protein concentration was not affected
 
==Data==
 
[[Image:Electrochemical_KI_Calibration_Curve.png]]


==Data==
Above is the calibration curve for [I<sup>-</sup>] created using the iodide ion selective electrode.
* Add data and results here...


==Notes==
==Notes==

Latest revision as of 00:28, 27 September 2017

Biomaterials Design Lab Main project page
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Create an Iodide Ion Selective Electrode

  • Prepare iodide ion selective electrodes
    • Prepare 10 mL 3 M NaCl
      • Carefully remove yellow plastic covering on Ag/AgCl electrode (as instructed)
      • Place electrode in 15 mL falcon tube with enough NaCl solution to match volume in electrode
      • cover and store upright until needed
    • Prepare 50 mL 4 M KNO3
      • Add KNO3 to outer double junction cell, filling narrow tube + ~ 0.5 inches further
      • Place electrode in small vial with enough KNO3 solution to cover the vycor tip
    • Prepare 50 mL 0.01 M KI + 0.1 M KNO3
      • Cut a short piece (~ 3 in) of silver wire
      • Place in KI/KNO3 solution
      • Electrolyze the solution using the power supply
      • The standard reduction potential for Ag/AgI is -0.15 V
      • Oxidation occurs at the anode, which is connected to the red lead
      • Electrolyze at low power (low current) until the wire appears coated
    • Test your electrodes with a range of KI solutions
      • The Ag/AgCl electrode slides inside of the KNO3 bridge solution (this is a double junction electrode)
      • The Ag/AgI wire can be connected directly to a multimeter using alligator clips
      • You will continue to connect your Ag wire to the red lead on the multimeter

Protocol taken from Dr. Fox.

Use this iodide ion selective electrode to create a calibration curve for [I-].

Additional Dialysis Analysis

Jake did the following:

  1. Ran Titration Analysis on KI-Colloid dialysis
  2. Ran Bradford Analysis on KI-Colloid dialysis

Description

  1. Titration
    1. Added 3mL 1M HNO3 and 0.5mL KI solution to 10mL DI H2O
    2. Added 2 mL AgNO3 and swirl to complete precipitation
    3. Added 200 μL Ferric alum indicator
    4. Titrate with your NH4SCN solution
  2. Ran Bradford Analysis on KI-Colloid dialysis
    1. As expected, the Bradford analysis held a constant protein concentration
      • Lysozyme is too big to pass through the 3500 MWCO so it was constant on one side
      • KI is not expected to react with lysozyme so protein concentration was not affected

Data

Above is the calibration curve for [I-] created using the iodide ion selective electrode.

Notes

This area is for any observations or conclusions that you would like to note.


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.