User:Andrew K Farag/Notebook/CHEM-582/2015/02/20: Difference between revisions

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==Entry title==
==Objectives==
* Insert content here...
*Bacterial Inactivation Evaluation in the Dark
 
==Bacterial Inactivation Evaluation in the Dark==
*the tubes containing the bacteria and broth were cloudy, confirming the growth of the bacteria
*Clean a TiO2/Epoxy film and an Epoxy film with ethanol to kill all bacteria
*Wash the TiO2/Epoxy film a few times to clean any TiO2 from the surface
*Clean lab tweezers with ethanol as well.  
*prepare two petri dishes for the films
*Make sure the film are dried out of the ethanol before placing them in the petri dish
*Vortex the broth/bacteria tubes
*Pipette 600 micro liter of the bacteria/broth solution onto the film
*try to even out the surface as much as you can
*Cover the petri dish so no evaporation occurs
*Place in drawer





Revision as of 12:48, 20 February 2015

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Objectives

  • Bacterial Inactivation Evaluation in the Dark

Bacterial Inactivation Evaluation in the Dark

  • the tubes containing the bacteria and broth were cloudy, confirming the growth of the bacteria
  • Clean a TiO2/Epoxy film and an Epoxy film with ethanol to kill all bacteria
  • Wash the TiO2/Epoxy film a few times to clean any TiO2 from the surface
  • Clean lab tweezers with ethanol as well.
  • prepare two petri dishes for the films
  • Make sure the film are dried out of the ethanol before placing them in the petri dish
  • Vortex the broth/bacteria tubes
  • Pipette 600 micro liter of the bacteria/broth solution onto the film
  • try to even out the surface as much as you can
  • Cover the petri dish so no evaporation occurs
  • Place in drawer