🔬 Nickel in Water

Physicochemistry PN-EN ISO 8288

In short

Determination of nickel in water by flame atomic absorption spectrometry (FAAS) at wavelength 232. The test is performed according to PN-EN ISO 8288:2002; Linear range: 0.02–5 mg/L. The procedure comprises 10 steps (about 1 h 1 min in total); it is used for: Control of electroplating wastewater (water permit), Monitoring of wastewater from metallurgy and metalworking, Testing of surface waters (Water Framework Directive).

At a glance

  • Standard: PN-EN ISO 8288:2002
  • Category: Physicochemistry
  • Procedure steps: 10
  • Total time of stages: 1 h 1 min
  • Wavelength: 232.0 nm
  • Flame type: acetylene-air (fuel-lean)
  • Detection limit (LOD): ~0.005 mg/L

Overview

Nickel (Ni) is a heavy metal of toxicological significance — it is one of the strongest contact allergens (nickel allergy affects about 10–15% of the population), and with chronic oral exposure can cause gastrointestinal disorders, kidney damage and carcinogenicity (nickel compounds — group 1 according to IARC). The permissible nickel concentration in drinking water is 20 µg/L (according to EU Directive 2020/2184 and MH Regulation).

Sources of nickel in waters are wastewater from electroplating (nickel plating), metallurgical industry (nickel steels, alloys), Ni-Cd and Ni-MH battery production, corrosion of stainless steel fittings, fossil fuel combustion, and natural leaching from nickel-bearing minerals.

Flame AAS (FAAS) is the basic method for determining nickel in waters at concentrations of 0.1–10 mg/L. The 232.0 nm resonance line is most commonly used, although the 341.5 nm line may be an alternative at higher concentrations. The acetylene-air flame provides sufficient energy for nickel atomization. The method is simple, fast and economical.

For concentrations below 0.02 mg/L (drinking water standard level), the FAAS technique is insufficient — GF-AAS (detection limit about 0.2 µg/L) or ICP-MS must be used. In laboratory practice, nickel in drinking water is determined mainly by GF-AAS or ICP-MS technique, and FAAS is used for wastewater control.

Method principle

A water sample acidified with HNO₃ is introduced through a nebulizer into an acetylene-air flame (about 2300°C). In the flame, the sample aerosol undergoes desolvation, thermal decomposition and atomization — free nickel atoms are formed. Ni atoms in the ground state absorb radiation from an HCL lamp at a wavelength of 232.0 nm (or alternatively 341.5 nm). Absorbance, proportional to Ni concentration (Beer-Lambert law), is measured by a detector and converted to concentration using a calibration curve.

Applications

Key parameters

ParameterValue
Wavelength232.0 nm
Flame typeacetylene-air (fuel-lean)
Detection limit (LOD)~0.005 mg/L
Limit of quantification (LOQ)~0.02 mg/L
Linear range0.02–5 mg/L
Sensitivity (characteristic concentration)~0.07 mg/L (1% absorption)

Standard

Standard number
PN-EN ISO 8288:2002
Title (PL)
Jakość wody — Oznaczanie kobaltu, niklu, miedzi, cynku, kadmu i ołowiu — Metody płomieniowej absorpcyjnej spektrometrii atomowej
Title (EN)
Water quality — Determination of cobalt, nickel, copper, zinc, cadmium and lead — Flame atomic absorption spectrometric methods

Step-by-step procedure

  1. Sample acidification

    Add HNO₃ 65% to pH <2 (1 mL per 100 mL sample). Store in PE/PP containers at 4°C.

    ⏱ Time: 5 min

  2. Preparation of standards

    Prepare calibration series: 0 (blank), 0.1, 0.5, 1.0, 2.0, 5.0 mg/L Ni in 1% HNO₃ from 1000 mg/L solution.

    ⏱ Time: 15 min

  3. Instrument setup

    Install Ni HCL lamp. Set wavelength 232.0 nm, slit 0.2 nm, lamp current 4 mA. Stabilize lamp 15 min.

    ⏱ Time: 15 min

  4. Ignition and flame optimization

    Ignite acetylene-air flame (flow: air 13.5 L/min, acetylene 2.0 L/min). Set fuel-lean flame (blue).

    ⏱ Time: 5 min

  5. Instrument calibration

    Aspirate blank and standards sequentially. Plot calibration curve. Correlation coefficient R² ≥0.999.

    ⏱ Time: 10 min

  6. Sample measurement

    Aspirate sample (approx. 5 mL/min). Read absorbance after stabilization (5–10 s). Aspirate 1% HNO₃ between samples (10 s).

    ⏱ Time: 1 min/sample

  7. Quality control

    Every 10 samples: blank (A <0.005), control standard (recovery 95–105%), duplicate (RPD <5%).

    ⏱ Time: 5 min

  8. Dilution of high concentration samples

    Dilute samples with concentration >5 mg/L to calibration range. Use 1% HNO₃ as diluting medium.

  9. Work closure

    Aspirate deionized water (2 min). Extinguish flame. Rinse nebulizer and spray chamber. Turn off lamp.

    ⏱ Time: 5 min

  10. Calculation and result reporting

    Ni concentration from calibration curve, considering dilution. Result in mg/L with 3 significant figures.

Required equipment and apparatus

EquipmentExampleIndicative price
Flame AAS spectrometerAgilent 240FS AA, Shimadzu AA-7000F, Analytik Jena novAA 800F60 000–180 000 PLN
Ni HCL lampAgilent Ni HCL, Heraeus, Photron — current 4 mA, slit 0.2 nm600–1 500 PLN
Technical acetyleneC₂H₂ 40 L cylinder, purity 2.6200–400 PLN/cylinder
Compressed airOil-free compressor with dryer and filter3 000–8 000 PLN
Sample aspiration systemConcentric nebulizer + Scott-type spray chamberincluded with instrument
Burner exhaust systemExhaust system with fan, connected to ventilation2 000–5 000 PLN

Reagents, media and consumables

ReagentCASDetails
Ni standard solution 1000 mg/L7440-02-0Certified CRM in 2% HNO₃ (Merck CertiPUR), traceable to NIST SRM
Nitric acid 65% analytical grade7697-37-2HNO₃ for acidifying samples and preparing standards; sample pH <2
Deionized waterQuality at least grade 2 according to PN-EN ISO 3696
Rinse solution 1% HNO₃For aspiration between samples to eliminate memory effect

Health and safety (OHS)

Frequently asked questions

Which standard describes this test?

The test is performed according to PN-EN ISO 8288:2002 — “Water quality — Determination of cobalt, nickel, copper, zinc, cadmium and lead — Flame atomic absorption spectrometric methods”.

How does this method work?

A water sample acidified with HNO₃ is introduced through a nebulizer into an acetylene-air flame (about 2300°C). In the flame, the sample aerosol undergoes desolvation, thermal decomposition and atomization — free nickel atoms are formed.

What is the measuring range and accuracy?

Wavelength: 232.0 nm; Flame type: acetylene-air (fuel-lean); Detection limit (LOD): ~0.005 mg/L; Limit of quantification (LOQ): ~0.02 mg/L.

How long does the test take?

The times given for the individual stages add up to approximately 1 h 1 min. The procedure comprises 10 steps.

What equipment is required?

Flame AAS spectrometer, Ni HCL lamp, Technical acetylene, Compressed air, Sample aspiration system, Burner exhaust system. Indicative cost of the core instrument (Flame AAS spectrometer): 60 000–180 000 PLN.

Where is this test used?

Control of electroplating wastewater (water permit); Monitoring of wastewater from metallurgy and metalworking; Testing of surface waters (Water Framework Directive); Drinking water quality control (Ni ≤20 µg/L — by GF-AAS technique); Analysis of mine waters; Control of stainless steel corrosion in water installations; Testing of groundwater at waste disposal sites.

What safety precautions apply?

Nickel compounds — carcinogenic (H350i — inhalation), strongly sensitizing (H317) — gloves and goggles mandatory; Acetylene — flammable and explosive gas, cylinder in vertical position, away from heat sources; Nitric acid — corrosive, work under fume hood; AAS flame — temperature ~2300°C, burner exhaust hood mandatory; Nickel-containing waste — collect separately, do not pour into sewage.

Which laboratory can perform this test?

The test is performed by laboratories accredited to ISO/IEC 17025. On LabCoda you can find them by the standard number PN-EN ISO 8288.

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