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ElyxirAuthorised ELIT Reseller

Barium

Ba²⁺

The ELIT barium electrode requires a unique still-solution measurement protocol and Standard Addition for samples with high ionic strength, due to interference from common ISAB constituents.

Cation (+)ELIT 8081Valence: Divalent
Electrode Specifications
Model
ELIT 8081
Membrane Type
Solid-state PVC polymer matrix membrane
Ion Type
Monovalent cationDivalent cation
Molar Mass
137.327 g/mol — 1000 ppm = 0.007 M
Physical Size
130 mm body (excl. contact) × 8 mm diameter. DC resistance < 2.5 MΩ at 25°C. Min. sample volume: 5 ml.
Operational Specifications
Concentration Range
0.5 to 13,700 ppm (4×10⁻⁶ to 0.1 Molar)
Electrode Slope at 25°C
21 ± 3 mV/decade
pH Range
pH 3 to 10
Temperature Range
0 to 50°C
Response Time
< 10 seconds (90% response)
Potential Drift
< 3 mV/day in 1000 ppm (8 hours)
Reagents
Reference Electrode
Single junction AgCl (ELIT 001).
ISAB / Buffer
NONE — the barium electrode is interfered with by the most common ISAB constituents. For high ionic strength samples, use the Standard Addition or Sample Addition method.
Standard Preparation
Dissolve 1.779g barium chloride dihydrate (BaCl₂·2H₂O) in 1 litre deionised water.
Interference

The Selectivity Coefficient (SC) represents the approximate apparent increase in the measured concentration caused by 1 unit of the interferent. Effect (% error) = (interferent concentration × SC / analyte concentration) × 100.

Interfering IonSelectivity CoefficientNotes
Strontium (Sr²⁺)0.09Highest interferent — unlikely in most samples.
Potassium (K⁺)0.02Significant error if K > 10× Ba concentration.
Sodium (Na⁺)0.02Significant error if Na > 10× Ba concentration.
Magnesium (Mg²⁺)0.006Tolerated up to ~20× Ba concentration.
Ammonium (NH₄⁺)0.003
Calcium (Ca²⁺)0.002Tolerated up to ~50× Ba concentration.
Lithium (Li⁺)0.002Tolerated up to ~50× Ba concentration.
Standard Analytical Method

Apparatus Required

  • Ion-Selective Electrode: ELIT 8081
  • Reference electrode: Single junction AgCl (ELIT 001)
  • Dual electrode head (ELIT 201)
  • ELIT Computer Interface/Ion Analyser, or Ion/pH/mV meter
  • 150 ml polypropylene beakers, 100 ml volumetric flask, 1, 2, 5, 10 ml pipettes

Calibration

For low ionic strength samples, use Direct Potentiometry with full calibration (1, 10, 100, 1000 ppm Ba). For high ionic strength, use Standard Addition: calibrate to find the slope, then enter slope and expected concentration into the software.

Sample Preparation & Measurement

Measurements must be made in still (unstirred) solutions. After immersion, manually swirl beaker for ~30 seconds, then leave to stand. Record mV at the lowest point before values start to rise again (typically < 2 mins for 10 ppm and above; up to 5 mins for < 1 ppm).

Results

Results are displayed as ppm and mol/l. If buffer solution has been added equally to standards and samples, figures will not need adjusting as all are affected by the same dilution factor. Allow 2–3 minutes stabilisation after electrode immersion. Wash and dry electrodes between samples to avoid cross-contamination.

Analytical Notes
  • Unlike most ISEs, barium MUST be measured in still (not stirred) solutions.
  • No ISAB is recommended — common ISAB constituents (K, Na, NH₄) interfere with the barium electrode.
  • Divalent cation — slope (~21 mV/decade) is slightly lower than a pure Nernstian response for a divalent ion.