What is ISO 12625-4?+
It is the international method for the dry tensile properties of tissue paper and tissue products. A strip (50,0 ± 0,5) mm wide is stretched to break over a (100 ± 1) mm span at a constant rate of elongation, and the method reports tensile strength in newtons per metre, stretch at maximum force as a percentage, and tensile energy absorption, plus the tensile index and tensile energy absorption index calculated against grammage. The current edition is ISO 12625-4:2022, the third, which cancels the withdrawn 2016 edition.
What is ISO 12625-5, and how does it differ?+
It is the companion method for wet tensile strength, currently ISO 12625-5:2024. The same strip is soaked with water immediately before the pull rather than tested dry. On a vertical machine the piece is looped under the rod of a Finch Cup soaking device held in the lower clamp, the water container is raised so the rod is immersed to (20 ± 1) mm, and after 15 s it drops away and the pull begins at (50 ± 2) mm/min. A horizontal machine uses a soaking device placed between the clamps instead.
What is wet-tensile-strength retention?+
The wet tensile strength expressed as a percentage of the dry tensile strength of a different test piece from the same sample, conditioned to ISO 187. It is the number that matters commercially for anything meant to be used wet: a sheet that is strong dry and collapses when wetted fails in the hand, and only the ratio shows that. Note that it compares two different test pieces from one sample rather than one piece tested twice.
Why are machine and cross direction reported separately?+
Because tissue is strongly anisotropic — the fibres orient with the machine direction, and the two directions can differ by a large factor. Both parts require the results to be calculated and reported separately for each direction. A single averaged figure hides whichever direction is weaker, which is the direction that will tear in service.
What load cell does a tissue tensile test need?+
A low-range one, chosen for the specimen. Part 4 requires the force-measuring system to be accurate to ±1 % of the reading or ±0,025 N, whichever is greater, verified to ISO 7500-1, and the apparatus to conform to ISO 1924-2. That 0,025 N floor is the specification that decides the machine: a cell sized for the frame's capacity rather than for a few newtons of tissue simply cannot resolve the result.
Why is the clamping force limited?+
Because tissue crushed at the jaw breaks at the jaw. Part 4 states that the test piece shall not be clamped with a force greater than 0,25 N, which is 5 N/m across the 50 mm width, and requires the clamps to have a means of adjusting that force. The clamps must also be at least 50 mm wide and grip along a straight line across the full width without damaging the sheet, with the clamping lines parallel within 1°.
What happens to specimens that break at the clamp?+
They are discarded and replaced. Under Part 4 a break within 5 mm of the clamping line does not count; under Part 5 the exclusion is a break within 2 mm of the upper clamp or on the rod. Testing continues until 10 valid results are available in each direction. If more than 20 % of the pieces cut from one specimen break that way, every reading from that specimen is rejected and the apparatus is inspected — the pattern points at the grips rather than the tissue.
What is accelerated ageing, and when is it used?+
It is a heat treatment, also called curing or rapid ageing, that develops the strength a wet-strength agent would otherwise reach over weeks of natural ageing. Part 5 gives (80 ± 2) °C for 30 min followed by at least an hour of conditioning, or (105 ± 2) °C for 15 min where production data are needed quickly. It is optional and the user decides, but the report has to state whether it was done and by what procedure, because an aged and an unaged result are not comparable.