User:Asya L. Tucker/Notebook/Asya 571/2015/09/16: 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:
==Procedure==
==Procedure==
To Prep 1 mL fiber samples
To Prep 1 mL fiber samples
## We centrifuge our samples and removed the supernatant  
# We centrifuge our samples and removed the supernatant  
## We left the tubes open so that rest of the water can evaporate
# We left the tubes open so that rest of the water can evaporate


To prepare a 500 mL of 10 mM Tris buffer at pH 9
To prepare a 500 mL of 10 mM Tris buffer at pH 9
Line 28: Line 28:


To prepare a 500 mL of 10 mM phosphate buffer at pH 7
To prepare a 500 mL of 10 mM phosphate buffer at pH 7
##sodium phosphate monobasic, MM = 137.99 g/mol
#sodium phosphate monobasic, MM = 137.99 g/mol
##potassium phosphate dibasic: 174.18 g/mol
#potassium phosphate dibasic: 174.18 g/mol
#Need 0.0005mol of each to make the solution.
#Need 0.0005mol of each to make the solution.
#Weigh 0.398g of sodium phosphate monobasic. Actual amount weighed: 0.40053g
#Weigh 0.398g of sodium phosphate monobasic. Actual amount weighed: 0.40053g
Line 45: Line 45:
   Number of moles: (10<sup>-3 </sup> mol/L)/2 = (5<sup>-4</sup>) mol  
   Number of moles: (10<sup>-3 </sup> mol/L)/2 = (5<sup>-4</sup>) mol  
   Amount of solute needed: MM of solute·(5*10<sup>-4</sup>) mol = amount that should be weighed
   Amount of solute needed: MM of solute·(5*10<sup>-4</sup>) mol = amount that should be weighed
==Results==
The final pH and conductivity reading for the tris buffer was 9.01 and 293 μS/cm.
The final pH and conductivity reading for the phosphate buffer was 6.89 and 14.63 μS/cm.


<!-- ##### 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 01:10, 27 September 2017

Project name Main project page
Previous entry      Next entry

Objective

  1. Prep 1 mL fiber samples for analysis
  2. Make 500 mL of 10 mM Tris buffer, pH 9
  3. Make 500 mL of 10 mM phosphate buffer, pH 7

Procedure

To Prep 1 mL fiber samples

  1. We centrifuge our samples and removed the supernatant
  2. We left the tubes open so that rest of the water can evaporate

To prepare a 500 mL of 10 mM Tris buffer at pH 9

  1. Make a 500mL solution of 10mM Tris Buffer, pH 9
  2. Weigh 0.06057g of Tris powder. Actual amount weighed: 0.0629g
  3. In a 500mL volumetric flask, add approximately 300mL of water, and a stirring pill
  4. Add the weighed powder
  5. Fill up to the 500mL mark using a pipette
  6. Place on stirring plate, and let it stir for a few minutes
  7. Measure conductivity and pH
  8. If first pH reading is not 9, add HCl until wanted pH is measured

To prepare a 500 mL of 10 mM phosphate buffer at pH 7

  1. sodium phosphate monobasic, MM = 137.99 g/mol
  2. potassium phosphate dibasic: 174.18 g/mol
  3. Need 0.0005mol of each to make the solution.
  4. Weigh 0.398g of sodium phosphate monobasic. Actual amount weighed: 0.40053g
  5. Weigh 0.368g of potassium phosphate dibasic. Actual amount weighed: 0.36682g
  6. In a 500mL volumetric flask, add approximately 300mL of water, and a stirring pill.
  7. Add both the sodium phosphate monobasic, and the potassium phosphate dibasic.
  8. Fill up to the 500mL mark using a pipette.
  9. Place on stirring plate, and let it stir for a few minutes.
  10. Measure conductivity and pH.
  11. If first pH reading is not very close to 7, or 7, add either potassium phosphate dibasic or sodium phosphate monobasic to reach the desired pH.

Calculations:

  Wanted concentration: 10mM = (10-3)M = 10(-3) mol/L 
  Wanted volume: 500mL = 0.5L
  Number of moles: (10-3  mol/L)/2 = (5-4) mol 
  Amount of solute needed: MM of solute·(5*10-4) mol = amount that should be weighed

Results

The final pH and conductivity reading for the tris buffer was 9.01 and 293 μS/cm. The final pH and conductivity reading for the phosphate buffer was 6.89 and 14.63 μS/cm.