ISO 17190-2:2021
Urine-absorbing aids for incontinence — Polyacrylate superabsorbent powders — Part 2: Test method for determination of the amount of residual acrylate monomers
Urine-absorbing aids for incontinence — Polyacrylate superabsorbent powders — Part 2: Test method for determination of the amount of residual acrylate monomers
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 10
- Дата публикации:
- 18 февраля 2021 г.
- Издание:
- ISO IS 17190 edition 2 version 1
- ICS:
- 11.180.20
This document provides a test method for determining the sum of residual monomeric sodium acrylate and acrylic acid present in polyacrylate superabsorbent powders as acrylic acid.
Abstract
Overview
ISO 17190-2:2021 specifies a laboratory test method to determine the sum of residual monomeric sodium acrylate and acrylic acid present in polyacrylate superabsorbent powders used in urine‑absorbing aids (incontinence products). The result is reported as acrylic acid. The method uses solvent extraction followed by HPLC (high‑performance liquid chromatography) quantification and is applicable to routine quality control, product development and regulatory compliance testing.
Key Topics
- Scope & principle: Extraction of residual monomers from superabsorbent powder and HPLC analysis to quantify residual acrylate monomers as acrylic acid. The standard uses a 1 g : 200 ml mass:volume dilution as the reference dilution factor.
- Reagents & solvents: Grade‑specified water (ISO 3696), 0.9 % sodium chloride saline, phosphoric acid (diluted to 0.1 % w/w), acetonitrile (HPLC grade), and high‑purity acrylic acid reference material (>99.5 %).
- Calibration & standards: Preparation of calibration solutions (example concentrations: S3 = 1 mg/L, S4 = 2 mg/L, S5 = 3 mg/L, S6 = 4 mg/L). Calibration analyses are run in duplicate; duplicate peak areas must agree within 5% or be repeated.
- Apparatus & chromatography: HPLC system with C18 column (e.g., 100 mm × 4.6 mm, 5 µm), guard column, UV detector at 210 nm, injection volumes 10–100 µL, and 0.45 µm PTFE filtration for sample cleanup.
- Sampling & conditioning: Samples conditioned to laboratory atmosphere (preferred (23 ± 2) °C and (45 ± 15) % RH per ISO 187). Homogenize containers by gentle rotation; ensure no lumps >1 mm.
- Safety & handling: Warnings on concentrated acids and respirable superabsorbent dust; reference to MAK guideline (respirable fraction <10 µm) indicating precautionary measures for dust exposure.
Applications
- Quality control testing by manufacturers of incontinence products, disposable hygiene products and suppliers of superabsorbent polymers (SAP).
- Independent testing laboratories performing conformity, safety and chemical‑residual verification.
- R&D teams optimizing polymerization processes to minimize residual monomers and ensure product safety.
- Regulatory bodies and procurement teams requiring validated test data for material acceptance.
Related Standards
- ISO 17190 series (other parts cover related test methods and characterization of urine‑absorbing aids)
- ISO 187 - environmental conditioning and sample atmosphere
- ISO 3696 - water for analytical laboratory use
ISO 17190-2:2021 is a practical, HPLC‑based standard for accurately quantifying residual acrylate monomers in polyacrylate superabsorbent powders, supporting product safety, compliance and process optimization.
Технические детали
- Технический комитет
- ISO/TC 173/SC 3 - Aids for ostomy and incontinence
- SKU
- ISO 17190-2:2021
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