Cary Eclipse fluorescence spectrometer: Difference between revisions
No edit summary |
(Add categories, improve list formatting) |
||
| Line 15: | Line 15: | ||
==Getting started-Scan== |
==Getting started-Scan== |
||
# Turn on the device and turn on the computer; don’t start the software immediately. |
|||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
==Scanning Set-Up== |
==Scanning Set-Up== |
||
| Line 49: | Line 46: | ||
'''II''' |
'''II''' |
||
Set the voltage of the PMT detector to have a better resolution of the low intensity signals. |
Set the voltage of the PMT detector to have a better resolution of the low intensity signals. |
||
[[Category:Geräte_-_Devices]] |
|||
[[Category:F&E4]] |
|||
Latest revision as of 12:58, 15 September 2017
Device name: Cary Eclipse fluorescence spectrometer
Device responsible: Nicolò Baroni
Room: R203
Wavelength range Excitation: 190 - 1100 nm
Wavelength range Emission: 190 - 1100 nm
Dimensions (W x D x H): 560 mm x 560 mm x 250 mm
Getting started-Scan
- Turn on the device and turn on the computer; don’t start the software immediately.
- Open the folder on desktop "Cary Eclipse" and choose the task "Scan".
- Go to scan set-up to put the desired setting (see below).
- Press Ok and then press the start button to start the measurement.
Scanning Set-Up
I Three modes of operation are offered: fluorescence, phosphorescence and bio-/chemi-luminescence.
II Select the measurement to perform: excitation, emission and synchronous (scans with a constant wavelength or wavenumber difference between monochromators to resolve multi-component mixtures).
III Select to scan in wavelength, wavenumber, angstroms or electron volts.
IV Set excitation and starting and ending wavelengths.
V Precise control over how much signal averaging is done and how frequently data points are collected.
I Set excitation and emission filter.
II Set the voltage of the PMT detector to have a better resolution of the low intensity signals.