Protocol for saltwater stable isotope analysis on Picarro: Difference between revisions

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- Use BERM for drift<br>
- Use BERM for drift<br>
- Use DI2 and EVAP2 for sample calibration<br>
- Use DI2 and EVAP2 for sample calibration<br>
- Prepare once for a whole set of runs, using inset vials (300 uL)
- Prepare once for a whole set of runs, using inset vials (300 uL)<br>
<br>
<br>
'''2. Run setup'''
'''2. Run setup'''
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- Insert BERM as drift standard after 8 samples<br>
- Insert BERM as drift standard after 8 samples<br>
- Repeat 3x for total 24 samples, with 2 drift samples in between, takes up 29 spots<br>
- Repeat 3x for total 24 samples, with 2 drift samples in between, takes up 29 spots<br>
- Rinse syringe with extra sample in position #43, after 10 samples
- Rinse syringe with extra sample in position #43, after 10 samples<br>
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<br>
'''3. Select method'''
'''3. Select method'''
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- Standards: 14 injections (12 in data file)<br>
- Standards: 14 injections (12 in data file)<br>
- Samples: 8 injections (6 in data file)
- Samples: 8 injections (6 in data file)<br>
<br>
<br>
'''5. Rinsing method'''
'''5. Rinsing method'''


- 5 injections, results in one small injection of rinse sample due to single wet peak routine
- 5 injections, results in one small injection of rinse sample due to single wet peak routine<br>
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<br>
'''6. Equipment cleaning'''
'''6. Equipment cleaning'''
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- Salt mesh exchanged after 24 samples, clean in ultrasonic bath, dry in glass oven, keep with septa<br>
- Salt mesh exchanged after 24 samples, clean in ultrasonic bath, dry in glass oven, keep with septa<br>
- Septum washed after each run, exchanged if needed after inspection<br>
- Septum washed after each run, exchanged if needed after inspection<br>
- Syringe washing in DI before and after run, repeated strokes until flow is smooth, moving plunger up and down over whole volume
- Syringe washing in DI before and after run, repeated strokes until flow is smooth, moving plunger up and down over whole volume<br>

Latest revision as of 14:14, 1 September 2020

Liquid run setup salt water

1. Prepare standards

- Use BERM for drift
- Use DI2 and EVAP2 for sample calibration
- Prepare once for a whole set of runs, using inset vials (300 uL)

2. Run setup

- Sequence from DI2 to BERM to EVAP2
- Define blocks of 8 samples
- Insert BERM as drift standard after 8 samples
- Repeat 3x for total 24 samples, with 2 drift samples in between, takes up 29 spots
- Rinse syringe with extra sample in position #43, after 10 samples

3. Select method

- Single wet peak, requires 2 extra injections, peak goes to waste (salt)
- FARLAB_Rinse_2, strokes, small injection

4. Number of Injections

- Standards: 14 injections (12 in data file)
- Samples: 8 injections (6 in data file)

5. Rinsing method

- 5 injections, results in one small injection of rinse sample due to single wet peak routine

6. Equipment cleaning

- Salt mesh exchanged after 24 samples, clean in ultrasonic bath, dry in glass oven, keep with septa
- Septum washed after each run, exchanged if needed after inspection
- Syringe washing in DI before and after run, repeated strokes until flow is smooth, moving plunger up and down over whole volume