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

From farlabprotocols
No edit summary
No edit summary
Line 5: Line 5:
- Use BERM for drift
- Use BERM for drift


- DI2 and EVAP2 for sample calibration
- Use DI2 and EVAP2 for sample calibration


- Prepare once in inset vials before a set of runs
- Prepare once for a whole set of runs, using inset vials (300 uL)


'''2. Run setup'''
'''2. Run setup'''


- Order DI2, BERM, EVAP2
- Sequence from DI2 to BERM to EVAP2


- Blocks of 8 samples
- Define blocks of 8 samples


- BERM drift standard
- Insert BERM as drift standard after 8 samples


- Repeat 3x for total 24 samples, with 2 drift samples in between, takes up 29 spots
- Repeat 3x for total 24 samples, with 2 drift samples in between, takes up 29 spots

Revision as of 14:11, 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