ISO 12193:2004
Animal and vegetable fats and oils — Determination of lead by direct graphite furnace atomic absorption spectroscopy
Animal and vegetable fats and oils — Determination of lead by direct graphite furnace atomic absorption spectroscopy
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 7
- Дата публикации:
- 14 января 2004 г.
- Издание:
- ISO IS 12193 edition 2 version 1
- ICS:
- 67.200.10
ISO 12193:2004 specifies a method for the determination of trace amounts (greater than 0,001 mg/kg) of lead in all types of crude or refined edible oils and fats.
Abstract
Overview
ISO 12193:2004 defines a validated analytical method for the determination of trace amounts of lead (Pb) in all types of crude or refined edible animal and vegetable fats and oils. The method uses direct graphite furnace atomic absorption spectroscopy (GFAAS / graphite furnace AAS) and is applicable for concentrations greater than 0.001 mg/kg (LOD) with a limit of determination of 0.01 mg/kg (LOQ). The procedure includes sample preparation, instrument settings, calibration and result reporting tailored for oil and fat matrices.
Key topics and technical requirements
- Principle: Atomize oil/fat samples in a graphite furnace and measure absorbance at 283.3 nm against organometallic lead standards.
- Sample preparation:
- Use metal‑free containers and store samples in polyethylene bottles.
- Typical test portion: 5.0 g sample mixed with 5.0 g matrix modifier.
- Matrix modifier: 2% lecithin solution in cyclohexane (analytical grade).
- Preheat samples in an oven at 60 °C prior to analysis.
- Standards & calibration:
- Use organometallic lead stock dissolved in blank oil; prepare working standards (e.g., 0.02, 0.05, 0.10 mg/kg) by dilution in blank oil.
- Construct a calibration curve corrected for blank.
- Instrumentation:
- GFAAS with background correction (deuterium or Zeeman) and appropriate hollow‑cathode or ED‑lamp for Pb.
- Argon gas of minimum 99.99% purity.
- Option to use pyrolytic-coated tubes and pyrolytic platform for improved sensitivity (platform improves accuracy and sensitivity roughly twofold).
- Injection volume: 20 µl.
- Recommended temperature programming and gas flow profiles are specified for uncoated and pyro-coated tubes.
- Quality and performance:
- Limit of detection: 0.001 mg/kg; limit of determination: 0.01 mg/kg.
- Interlaboratory study shows negligible bias in the 0.01–0.10 mg/kg range; repeatability and reproducibility limits are provided.
Practical applications
- Routine food safety testing for lead contamination in edible oils (olive oil, soybean oil, cocoa butter, etc.).
- Quality control in oil refining and processing plants to verify compliance with regulatory limits.
- Regulatory and national food laboratories performing trace metal surveillance and compliance testing.
- Method reference for laboratories implementing GFAAS procedures for trace lead measurement in lipid matrices.
Who should use this standard
- Food and beverage analytical laboratories
- Oil and fat producers and refiners (QC/QA teams)
- Regulatory authorities and inspection labs
- Accredited testing laboratories seeking validated procedures for lead in fats and oils
Related standards
- ISO 5555:2001 - Sampling of animal and vegetable fats and oils (recommended sampling guidance).
- ISO 5725 (referenced) - Precision of measurement methods (used for interlaboratory evaluation).
Keywords: ISO 12193, lead determination, graphite furnace atomic absorption spectroscopy, GFAAS, edible oils, trace lead, matrix modifier, limit of detection, oil testing.
Технические детали
- Технический комитет
- ISO/TC 34/SC 11 - Animal and vegetable fats and oils
- SKU
- ISO 12193:2004
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