Difference between revisions of "User:Michael F. Nagle/Notebook/Chem 571/2012/10/31"

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
 
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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|style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
 
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*Samples from 134-140 showed variation in the background. In order to determine whether this was due to Lysozyme or variation in cuvettes, these trials were repeated using the same quartz cuvette. A blank of water was run using the same cuvette and subtracted from each spectra manually.
 
*Samples from 134-140 showed variation in the background. In order to determine whether this was due to Lysozyme or variation in cuvettes, these trials were repeated using the same quartz cuvette. A blank of water was run using the same cuvette and subtracted from each spectra manually.
 
*[[User:Puja_Mody/Notebook/Chem_571:_Gold_Nanoparticles/2012/10/31|Puja Moody]] purified ADA from E. Coli grown [[User:Michael_F._Nagle/Notebook/Chem_571/2012/10/23|last week]]
 
*[[User:Puja_Mody/Notebook/Chem_571:_Gold_Nanoparticles/2012/10/31|Puja Moody]] purified ADA from E. Coli grown [[User:Michael_F._Nagle/Notebook/Chem_571/2012/10/23|last week]]
 
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==Data==
 
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[[Image:Quartzlys.jpg]]
 
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==Discussion==
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*In the abs. vs mole ratio plot for the first round, done using plastic cuvettes, a jagged line is seen from 134-140. A significant change in backgrounds is seem on the wavelength vs. absorbance graph. Because of this, we analyzed these samples again using quartz cuvettes.
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*Starting at 100, an increasing amount of AuNPs appear in solution. This peaks at 140 before decining to near-zero at 170. This indicates that the optimal mole ratio for AuNPs in solution is 140 and that they start to go into fibers at higher mole ratios.
 
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Latest revision as of 21:11, 26 September 2017

Owwnotebook icon.png Project name Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png

Objectives

  • Obtain UV/Vis spectra for Au/Lysozyme samples with varying mole ratios.
  • Purify ADA from E. Coli

Procedure

  • Au/Lysozyme samples prepared last Wednesday were analyzed by UV/Vis using disposable plastic cuvettes. The instrument held a blank cuvette of water, which was automatically subtracted from the spectra of the Au/Lysozyme.
  • Samples from 134-140 showed variation in the background. In order to determine whether this was due to Lysozyme or variation in cuvettes, these trials were repeated using the same quartz cuvette. A blank of water was run using the same cuvette and subtracted from each spectra manually.
  • Puja Moody purified ADA from E. Coli grown last week

Data

Quartzlys.jpg

Discussion

  • In the abs. vs mole ratio plot for the first round, done using plastic cuvettes, a jagged line is seen from 134-140. A significant change in backgrounds is seem on the wavelength vs. absorbance graph. Because of this, we analyzed these samples again using quartz cuvettes.
  • Starting at 100, an increasing amount of AuNPs appear in solution. This peaks at 140 before decining to near-zero at 170. This indicates that the optimal mole ratio for AuNPs in solution is 140 and that they start to go into fibers at higher mole ratios.