December 26, 2024, 11:29:45 AM
Forum Rules: Read This Before Posting


Topic: Thesis method not working - cadmium detecton using Alizarin red s dye  (Read 3327 times)

0 Members and 2 Guests are viewing this topic.

Offline mia1530

  • Very New Member
  • *
  • Posts: 1
  • Mole Snacks: +0/-0
  • Gender: Female
Hi guys!
So I'm working on a method for cadmium detection using a dye Alizarin red s, but the method is not giving me the expected results (a linear increase in absorbance with increasing concentration of cadmium)

The pKa of alizarin red S is 4.5, and I have been carrying the method out in a 10ml solution, of which 1ml is 0.05M sulfuric acid (as per source paper) I have increased the acid volume in the sample, to no avail. The method also stated that it was a 1:2 stochiometry of dye:cadmium.

I think I'm working at a pH above 4.5, so my dye should be deprotenating sufficiently for it to bind to the cadmium, but I am not sure, and do not have access to the lab to  test the pH of the solution. But beyond this, I cannot think of any reason why the method does not work. I'm a little worried that a step was left out of the method, as I need to be able to explain why I think it may not have worked for my final write up.

Does anyone have any ideas? I have attached the structure according to the source paper.

Any help would really be appreciated!

Offline Corribus

  • Chemist
  • Sr. Member
  • *
  • Posts: 3551
  • Mole Snacks: +546/-23
  • Gender: Male
  • A lover of spectroscopy and chocolate.
I think I'm working at a pH above 4.5,
Never good to assume. On what basis do you think this?

You don't need pH paper to get a good estimate. If you have 10 mL of solution and 1 mL is 0.05 M H2SO4, what is the pH? Just for a quick estimate, ignore the second deprotonation.
What men are poets who can speak of Jupiter if he were like a man, but if he is an immense spinning sphere of methane and ammonia must be silent?  - Richard P. Feynman

Offline kriggy

  • Chemist
  • Sr. Member
  • *
  • Posts: 1520
  • Mole Snacks: +136/-16
Seems weird to work in acidic medium when you need to deprotonate those OH groups

Offline AWK

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 7976
  • Mole Snacks: +555/-93
  • Gender: Male
I do not know the exact Mia1530 source, but report in Journal of Chemical Engineering IEB
Vol. ChE. 25, No. 1, December 2010 pages 1-12 contains an evident printing error that causes 100 times lower concentration of Alizarin Red S (should be 1.39x10-1 M instead of 1.39x10-3 M.
Article in public domain:
https://www.google.pl/url?sa=t&rct=j&q=&esrc=s&source=web&cd=1&cad=rja&uact=8&ved=0CCgQFjAA&url=http%3A%2F%2Fwww.banglajol.info%2Findex.php%2FJCE%2Farticle%2Fdownload%2F7233%2F5452&ei=LYRlVdDyEcKssgH1gIKICg&usg=AFQjCNEqqAWyrG9i7hU6SIdoeDzl3d2tsQ&sig2=yu8GQLfoSsomJHXHhDxbgw&bvm=bv.93990622,d.bGg
AWK

Sponsored Links