Sensor types (what to buy, in one glance)

O₂ (oxygen)

  • Electrochemical (galvanic): ppm-level, compact; consumable cell, sensitive to solvents.
  • Optical (luminescence/quenching): ppm-level, solvent-tolerant options; higher cost, stable drift.
  • Zirconia / paramagnetic: robust percent-level monitoring; use as a backup or for purge lines.

Dew point / H₂O

  • Capacitive polymer: common, fast, good to about –60 °C DP; can wander with solvents.
  • Aluminum-oxide: good for very low DP; slower, rugged.
  • Chilled mirror: reference-grade accuracy; bigger, pricier; ideal as a lab standard to verify others.

Plain advice: If you chase ≤5 ppm O₂ and ≤–60 °C DP, pair optical O₂ + capacitive or Al₂O₃ DP, and keep a chilled mirror in the lab for periodic truth checks.


Placement & plumbing (this is where most errors start)

  • Location: mount probes in the main circulation loop, downstream of mixing, away from dead zones and glove turbulence.
  • Bypass line: use a low-dead-volume sample line with a small continuous flow; add a sintered guard filter.
  • Temperature: keep DP sampling lines slightly warmer than ambient to avoid condensation in the tube.
  • Solvents: shield intakes from open beakers; use charcoal/cold traps if vapor load is high.

Alarms & logging (practical defaults)

  • O₂: Warn 5 ppm, High 10 ppm (tighten for ultra-sensitive work).
  • Dew point: Warn –35 °C, High –30 °C.
  • Pressure sanity: keep +3–8 mbar; unstable pressure gives noisy sensor data.
  • Logs: record at shift start/end + events (large transfers, regen, trap changes). Review a 7-day trend weekly.

Fast calibration & checks (5–10 minutes)

O₂ (ppm probe)

  1. Zero: flow high-purity N₂/Ar over the sensor; confirm near-zero.
  2. Span: expose to a known span (e.g., clean air ≈20.9% for percent-type, or certified ppm span gas for ppm-type).
  3. Leak sanity: block inlet → verify reading stabilizes; if not, check fittings.

Dew point

  1. Dry check: verify near the instrument’s floor with a dry gas.
  2. Cross-check: compare to chilled mirror or a second probe in the same bypass.
  3. Response time: step from dry to ambient; confirm it responds smoothly (no sticking = filter clean).

Intervals (good starting point)

  • Weekly: quick zero check (O₂) + dry check (DP).
  • Quarterly: two-point calibration or cross-check vs chilled mirror; replace sample-line filters.
  • After events: re-check whenever you’ve had solvent incidents, sensor swap, plumbing changes.

Troubleshooting (symptom → cause → fix)

  • Readings noisy → sampling in a dead zone / pressure swings → move to main loop; stabilize at +3–8 mbar.
  • DP rising, O₂ flatsolvent vapor → lids on; refresh charcoal/cold traps; move probe intake.
  • Both drifting upleak or tired purifier → run leak test; review regeneration.
  • Slow responseclogged filter / wet line → replace filter; warm and dry the line.
  • Won’t zero → residual leaks in bypass / contaminated probe → tighten fittings; clean or replace guard/filter.