User:Mary Mendoza/Notebook/CHEM 581: Experimental Chemistry I/2014/09/24: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
(fix raw html notebook nav)
 
(2 intermediate revisions by one other user not shown)
Line 2: Line 2:
|-
|-
|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>}}
|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}}}}]]}}
|-
|-
| colspan="2"|
| colspan="2"|
Line 14: Line 14:
* 0.11024 g of (1-hexadecyl)triphenylphosphonium bromide (BEM's exchanged clay) was added to 1.00123 g of PVA
* 0.11024 g of (1-hexadecyl)triphenylphosphonium bromide (BEM's exchanged clay) was added to 1.00123 g of PVA
* These mixtures were stirred and heated. It was observed that the exchanged clay would not completely dissolve into solution.
* These mixtures were stirred and heated. It was observed that the exchanged clay would not completely dissolve into solution.
* At the end of the lab, 0.5 mL of 0.8 wt% glutaraldehyde was added. The mixtures were stirred at room temperature and then cast into teflon dishes.


==Suspension of Films in Rhodamine 6G==
==Suspension of Films in Rhodamine 6G==
* The arsenic, mercury, and lead were replaced with rhodamine 6G.
* The arsenic, mercury, and lead were replaced with rhodamine 6G.
* Stock dilutions of 159 μM rhodamine 6G into 1, 10, and 20 μM were prepared by James, Michael, and Eleni.  
* Stock dilutions of 159 μM rhodamine 6G into 1, 10, and 20 μM were prepared by James, Michael, and Eleni.
* The table for the masses of the films and vial are posted on Jacob Esenther's [[User:Jacob Esenther/Notebook/581/2014/09/24|page.]]
* The table for the masses of the films and vial are posted on Jacob Esenther's [[User:Jacob Esenther/Notebook/581/2014/09/24|page.]]  
* The following calculations for the dilution of rhodamine 6G are as follows, taken from Michael Bible's [[User:Michael S. Bible/Notebook/581/2014/09/24|entry:]]
 
====Preparation of solutions====
* The three concentrations of R6G were created from a stock solution of 159 μM R6G.
**1μM R6G - 0.629 mL of stock into 100mL - prepared by Eleni
**10μM R6G - 6.289 mL of stock into 100mL - prepared by Michael
**20μM R6G - 12.578mL of stock into 100mL - prepared by James
 
====Calculations====
 
V<sub>1</sub>*C<sub>1</sub> = V<sub>2</sub>C<sub>2</sub>
 
V<sub>1</sub> =  V<sub>2</sub>C<sub>2</sub>/C<sub>1</sub>
 
V<sub>stock</sub> = (100 mL)(1μM)/159μM) = 0.629 mL
 
V<sub>stock</sub> = (100 mL)(10μM)/159μM) = 6.289 mL
 
V<sub>stock</sub> = (100 mL)(20μM)/159μM) = 12.578 mL
 


<!-- ##### 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. ##### -->

Latest revision as of 00:20, 27 September 2017

Project name Main project page
Previous entry      Next entry

Measurements with AAS

  • Runs for arsenic and mercury samples are temporarily postponed due to technical issues such as defects with the detector and burnt out arsenic lamp.
  • Lead (II) acetate · 3 H2O was cancelled as well.

Films with Exchanged Clay

  • 0.11163 g of tributylhexadecylphosphonium phosphonium bromide (our exchanged clay) was added to 1.00888 g of PVA
  • 0.11024 g of (1-hexadecyl)triphenylphosphonium bromide (BEM's exchanged clay) was added to 1.00123 g of PVA
  • These mixtures were stirred and heated. It was observed that the exchanged clay would not completely dissolve into solution.
  • At the end of the lab, 0.5 mL of 0.8 wt% glutaraldehyde was added. The mixtures were stirred at room temperature and then cast into teflon dishes.

Suspension of Films in Rhodamine 6G

  • The arsenic, mercury, and lead were replaced with rhodamine 6G.
  • Stock dilutions of 159 μM rhodamine 6G into 1, 10, and 20 μM were prepared by James, Michael, and Eleni.
  • The table for the masses of the films and vial are posted on Jacob Esenther's page.
  • The following calculations for the dilution of rhodamine 6G are as follows, taken from Michael Bible's entry:

Preparation of solutions

  • The three concentrations of R6G were created from a stock solution of 159 μM R6G.
    • 1μM R6G - 0.629 mL of stock into 100mL - prepared by Eleni
    • 10μM R6G - 6.289 mL of stock into 100mL - prepared by Michael
    • 20μM R6G - 12.578mL of stock into 100mL - prepared by James

Calculations

V1*C1 = V2C2

V1 = V2C2/C1

Vstock = (100 mL)(1μM)/159μM) = 0.629 mL

Vstock = (100 mL)(10μM)/159μM) = 6.289 mL

Vstock = (100 mL)(20μM)/159μM) = 12.578 mL