SIST EN ISO 13884:2005
Animal and vegetable fats and oils - Determination of isolated trans isomers by infrared spectrometry (ISO 13884:2003)
Animal and vegetable fats and oils - Determination of isolated trans isomers by infrared spectrometry (ISO 13884:2003)
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 14
- Дата публикации:
- 1 декабря 2005 г.
- ICS:
- 67.200.10
- Технический комитет:
- KŽP - Agricultural food products
ISO 13884:2003 specifies a method for the accurate determination of isolated trans bonds in natural or processed long-chain fatty acids, fatty acid esters and triglycerides with trans isomer levels greater than or equal to 5 %. The method is not applicable, or is applicable only with specific precautions, to fats and oils containing high levels (over 5 %) of conjugated unsaturation (e.g. tung oil); materials containing functional groups which modify the intensity of the C-H deformation about the trans double bond [e.g. castor oil containing ricinoleic acid or its geometrical isomer, ricinelaidic acid (12-hydroxy-9-octadecenoic acid)]; mixed triglycerides having long- and short-chain moieties (such as diacetostearin); or in general, any materials containing constituents which have functional groups which give rise to specific absorption bands at or sufficiently close to interfere with the 966 cm-1 band of the C-H deformation of the isolated trans double bond.
Abstract
Overview
EN ISO 13884:2005 (identical to ISO 13884:2003) specifies an infrared spectrometric method for the accurate determination of isolated trans isomers in animal and vegetable fats and oils when trans levels are ≥ 5%. The method measures the C–H deformation band at 966 cm⁻¹, characteristic of isolated trans double bonds, and is adopted by CEN for use across European standards bodies.
Key topics and technical requirements
- Analyte and scope
- Long-chain fatty acids, fatty acid esters and triglycerides with isolated (non-conjugated) trans bonds.
- Not applicable (or only with precautions) to materials with >5% conjugated unsaturation (e.g., tung oil), functional groups that alter the 966 cm⁻¹ band (e.g., ricinoleic/ricinelaidic acids), mixed long/short-chain triglycerides, or other interfering absorptions.
- Principle
- Quantification is based on the IR absorption maximum at 966 cm⁻¹ (C–H deformation of isolated trans double bond).
- For higher accuracy, samples are converted to methyl esters prior to measurement to eliminate glycerol and carboxyl interferences.
- Instrumentation
- FT‑IR or dispersive IR spectrometer capable of 4 cm⁻¹ resolution over 1050–900 cm⁻¹.
- Liquid sampling cells with NaCl or KBr windows and 1 mm path length; matched cells or beam balancing required.
- Reagents and standards
- Dry carbon disulfide (CS2) solvent (handle with ventilation).
- Primary standards: methyl elaidate and methyl oleate (≈99% purity).
- Calibration prepared across multiple trans levels (1%, 4%, 7%, 10%, 30%, 50%, 70%) using specified stock solutions.
- Calibration & procedure
Applications and users
- Practical for food and oil quality control, processing evaluation (e.g., partial hydrogenation effects), and nutritional labeling where trans content ≥ 5% is relevant.
- Primary users: analytical laboratories, edible oil producers, regulatory agencies, research labs studying lipid isomerization and processing effects.
- Not recommended where conjugated dienes or interfering functional groups are present without specific validation.
Related standards
Технические детали
- SKU
- SIST EN ISO 13884:2005
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