E
ElyxirAuthorised ELIT Reseller

Ammonium

NH₄⁺

The ELIT ammonium electrode measures NH₄⁺ ions directly in aqueous solution without the need for alkaline pre-treatment. Suitable for water quality monitoring, environmental analysis, aquaculture, and agricultural applications.

Cation (+)ELIT 8051Valence: Monovalent
Electrode Specifications
Model
ELIT 8051
Membrane Type
Solid-state PVC polymer matrix membrane
Ion Type
Monovalent cation
Molar Mass
18.038 g/mol — 1000 ppm = 0.055 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
0.03 to 1,800 ppm (2×10⁻⁶ to 0.1 Molar)
Electrode Slope at 25°C
54 ± 5 mV/decade
pH Range
pH 0 to 8.5
Temperature Range
0 to 50°C
Response Time
< 10 seconds (90% response)
Potential Drift
< 3 mV/day in 1000 ppm (8 hours, constant temperature)
Reagents
Reference Electrode
Double junction lithium acetate (ELIT 003n). Outer filling solution: 0.1M CH₃COOLi.
ISAB / Buffer
1M CuSO₄ (Add 10% v/v). Use 1M MgSO₄ for NH₄ concentrations above 50 ppm.
Standard Preparation
Dissolve 2.965g anhydrous ammonium chloride (NH₄Cl) in 1 litre deionised water. Dry NH₄Cl for one hour at 100°C and cool in a desiccator before use for highest accuracy.
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
Potassium (K⁺)0.1Primary interferent — special correction required if K/NH₄ ratio > 0.5
Sodium (Na⁺)0.002
Magnesium (Mg²⁺)0.0002Note: 0.1M MgSO₄ ISAB can give apparent NH₄ signal up to 2 ppm — use CuSO₄ instead for samples < 50 ppm NH₄
Calcium (Ca²⁺)0.00006
Lithium (Li⁺)0.00003
Standard Analytical Method

Apparatus Required

  • Ion-Selective Electrode: ELIT 8051
  • Reference electrode: Double junction lithium acetate (ELIT 003n)
  • 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

Calibrate with serial dilutions of 1000 ppm standard: 1000, 100, 10, 1, 0.1 ppm NH₄. For high ionic strength samples (>0.01 M), add 10 ml ISAB to each 100 ml standard. Note: ISAB addition raises slope, raises lower detection limit, and lowers pH.

Sample Preparation & Measurement

Low ionic strength: no preparation required — immerse electrodes directly in 50–100 ml sample. High ionic strength: add 10 ml ISAB to 100 ml sample and stir well.

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.

Special Procedures

Samples with High Potassium Content (K/NH₄ > 0.5)

Rather than relying on the general selectivity coefficient, measure the interference directly: (1) measure NH₄ and K in a representative sample; (2) add additional K to double the concentration and remeasure the apparent NH₄; (3) calculate the selectivity coefficient from the increase. Alternatively, spike all standards with the same K concentration as the samples.


pH and Temperature Relationship

In aqueous solution there is a pH-dependent equilibrium between NH₄⁺ and NH₃. Below pH 6.5 there is essentially 100% NH₄⁺; above pH 11.5 essentially 100% NH₃. For Total Ammonia Nitrogen (TAN) measurements, keep pH below 7. For dissolved NH₃ toxicity, measure pH and temperature of each sample and calculate the NH₄/NH₃ ratio.

Analytical Notes
  • The ELIT ammonium electrode measures NH₄⁺ directly in solution — no pre-treatment with caustic chemicals or liberation of noxious gases is required.
  • Stir solutions gently during measurement; allow 2–3 minutes stabilisation after electrode immersion.
  • For highest precision, recalibrate frequently.
  • 1000 ppm standard is stable for extended periods; dilute working standards should be freshly prepared.