This document specifies a test method for the determination of the wet tensile strength of tissue paper and tissue products after soaking with water, using a tensile-strength-testing apparatus operating with a constant rate of elongation.
Currently, two types of tensile-strength-testing apparatus are commercially available, one where the test piece is positioned vertically and, for the other, horizontally. This document applies for both. For vertical tensile-strength-testing apparatus, a device that is held in the lower grip of the tensile-strength-testing apparatus, called a Finch Cup, is used to achieve the wetting. For horizontal tensile-strength-testing apparatus, the soaking device is placed between the two clamps.
This document is not applicable to cases where impurities and contraries are determined.

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This document specifies a test method for the determination of the wet tensile strength of tissue paper and tissue products after soaking with water, using a tensile-strength-testing apparatus operating with a constant rate of elongation.
Currently, two types of tensile-strength-testing apparatus are commercially available, one where the test piece is positioned vertically and, for the other, horizontally. This document applies for both. For vertical tensile-strength-testing apparatus, a device that is held in the lower grip of the tensile-strength-testing apparatus, called a Finch Cup, is used to achieve the wetting. For horizontal tensile-strength-testing apparatus, the soaking device is placed between the two clamps.
This document is not applicable to cases where impurities and contraries are determined.

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This document specifies the testing procedures for the instrumental determination of the opacity of tissue paper or tissue products by diffuse reflectance using a paper backing.
This document contains specific instructions for the preparation of test pieces of single-ply and multi-ply products, where special preparation/procedures might be necessary.
It can be used to determine the opacity of tissue paper and tissue products containing fluorescent whitening agents, provided the UV content of the radiation incident on the test piece has been adjusted to conform to that in the CIE illuminant C using a fluorescent reference standard provided by an authorized laboratory as described in ISO 2470-1.

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This document specifies a test method for the determination of the wet tensile strength of tissue paper and tissue products after soaking with water, using a tensile-strength-testing apparatus operating with a constant rate of elongation. Currently, two types of tensile-strength-testing apparatus are commercially available, one where the test piece is positioned vertically and, for the other, horizontally. This document applies for both. For vertical tensile-strength-testing apparatus, a device that is held in the lower grip of the tensile-strength-testing apparatus, called a Finch Cup, is used to achieve the wetting. For horizontal tensile-strength-testing apparatus, the soaking device is placed between the two clamps. This document is not applicable to cases where impurities and contraries are determined.

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This document specifies the testing procedures for the instrumental determination of the opacity of tissue paper or tissue products by diffuse reflectance using a paper backing.
This document contains specific instructions for the preparation of test pieces of single-ply and multi-ply products, where special preparation/procedures might be necessary.
It can be used to determine the opacity of tissue paper and tissue products containing fluorescent whitening agents, provided the UV content of the radiation incident on the test piece has been adjusted to conform to that in the CIE illuminant C using a fluorescent reference standard provided by an authorized laboratory as described in ISO 2470-1.

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  • Standard
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This document specifies the testing procedures for the instrumental determination of the opacity of tissue paper or tissue products by diffuse reflectance using a paper backing. This document contains specific instructions for the preparation of test pieces of single-ply and multi-ply products, where special preparation/procedures might be necessary. It can be used to determine the opacity of tissue paper and tissue products containing fluorescent whitening agents, provided the UV content of the radiation incident on the test piece has been adjusted to conform to that in the CIE illuminant C using a fluorescent reference standard provided by an authorized laboratory as described in ISO 2470-1.

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This document specifies a test method for the determination of the tensile strength of perforated lines of tissue paper. It uses a tensile-testing apparatus operating with a constant rate of elongation.
This method is only used for measuring machine-direction tensile strength, that is for cross-direction perforations on tissue paper.
The calculation of perforation efficiency is also specified in this document.

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SIGNIFICANCE AND USE
5.1 The plastic Petri plate (carrier) provides a closed system for enumeration and easy application of a pre-saturated or impregnated antimicrobial towelette by an analyst.  
5.2 Aliquoting of sterile 5 % non-heat-inactivated fetal bovine serum (five 10 µL spots) onto soiled carriers and inoculation of final test suspension onto treated carriers (five 10 µL spots) is conducted using a template and a positive displacement pipette, thereby ensuring a precise inoculum level and uniform distribution of soil and final test suspension.  
5.3 A single towelette is tested per 2-carrier set, eliminating the likelihood of cross contamination between carriers.  
5.4 The corkscrew-patterned circular motion of the product application (wipe outside to inside, wipe inside to outside using the wiping template; see Annex A3 – Annex A6) ensures uniform coverage and contact of disinfectant with the inoculated surface.  
5.5 The addition of neutralizer to the treated carriers at the end of the contact time results in neutralization of the test substance. This standard test method provides a procedure for performing neutralization verification to confirm that the microbicidal, microbistatic, or both types of activity of a test substance has been reduced by 50 % at the end of the contact time (see Annex A1 for neutralization verification procedure).  
5.6 The design of this standard test method minimizes any loss of viable organisms through carrier wash-off.  
5.7 It is optional to adjust (dilution in PBS) the inoculum to achieve desired control counts of 5.0 log10 CFU/carrier to 6.5 log10 CFU/carrier.  
5.8 Include, where applicable, comparisons of the test to other similar procedures such as Practices E1054 and E2362.
SCOPE
1.1 This test method quantitatively determines the effectiveness of various sizes of antimicrobial towelettes in treating hard, non-porous surfaces against Pseudomonas aeruginosa and Staphylococcus aureus.  
1.2 This test method may be used to evaluate towelettes for antimicrobial efficacy against additional microorganisms (with necessary modifications).  
1.2.1 This test method does not differentiate between chemical inactivation of the test microbe and mechanical removal of inoculum from a surface; rather, product efficacy is considered a combination of both attributes of a towelette-based formulation.  
1.3 This test method involves the use of hazardous materials, chemicals, and infectious microorganisms and therefore should be performed only by those trained in microbiological techniques in facilities designed and equipped for work with infectious agents at the appropriate biosafety level, a BSL-2 or higher laboratory; specifications provided in the “Biosafety for Biomedical and Microbiological Laboratories” (BMBL), 6th edition (BMBL).  
1.4 It is the responsibility of the investigator to determine whether Good Laboratory Practices (GLP Standards—For example, 40 CFR, Part 160 of FIFRA) are required and to follow them when appropriate.  
1.5 Strict adherence to the protocol is necessary for the validity of the test results.  
1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This document specifies a test method for the determination of the tensile strength of perforated lines of tissue paper. It uses a tensile-testing apparatus operating with a constant rate of elongation.
This method is only used for measuring machine-direction tensile strength, that is for cross-direction perforations on tissue paper.
The calculation of perforation efficiency is also specified in this document.

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This document specifies a test method for the determination of the tensile strength of perforated lines of tissue paper. It uses a tensile-testing apparatus operating with a constant rate of elongation. This method is only used for measuring machine-direction tensile strength, that is for cross-direction perforations on tissue paper. The calculation of perforation efficiency is also specified in this document.

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This document specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed in indoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions can be necessary.
NOTE      The properties called D65 brightness and colour are measured with an instrument adjusted to a much higher UV content than that specified in this document.

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This document specifies a test method for the determination of the surface friction of tissue paper and tissue products using a contact-type surface tester.

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This document specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed in indoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions can be necessary.
NOTE      The properties called D65 brightness and colour are measured with an instrument adjusted to a much higher UV content than that specified in this document.

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This document specifies a test method for the determination of the tensile strength, stretch at maximum force and tensile energy absorption of tissue paper and tissue products. It uses a tensile-testing apparatus operating with a constant rate of elongation.
It also specifies the method of calculating the tensile index and the tensile energy absorption index.

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This document specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed in indoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions can be necessary. NOTE The properties called D65 brightness and colour are measured with an instrument adjusted to a much higher UV content than that specified in this document.

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This document specifies a test method for the determination of the tensile strength, stretch at maximum force and tensile energy absorption of tissue paper and tissue products. It uses a tensile-testing apparatus operating with a constant rate of elongation.
It also specifies the method of calculating the tensile index and the tensile energy absorption index.

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This document specifies a test method for the determination of the tensile strength, stretch at maximum force and tensile energy absorption of tissue paper and tissue products. It uses a tensile-testing apparatus operating with a constant rate of elongation. It also specifies the method of calculating the tensile index and the tensile energy absorption index.

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This document specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed under outdoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions can be necessary.
NOTE       The properties called ISO brightness and colour with C/2° (indoor daylight) are measured with an instrument adjusted to a much lower UV content than that specified in this document. The measurements of ISO brightness and colour with C/2° (indoor daylight) are described in ISO 12625-15.

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This document specifies a method to assess the disintegration of tissue paper and tissue products when subjected to mechanical agitation in water.

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This document specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed under outdoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions can be necessary.
NOTE       The properties called ISO brightness and colour with C/2° (indoor daylight) are measured with an instrument adjusted to a much lower UV content than that specified in this document. The measurements of ISO brightness and colour with C/2° (indoor daylight) are described in ISO 12625-15.

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This document specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed under outdoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions can be necessary. NOTE The properties called ISO brightness and colour with C/2° (indoor daylight) are measured with an instrument adjusted to a much lower UV content than that specified in this document. The measurements of ISO brightness and colour with C/2° (indoor daylight) are described in ISO 12625-15.

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This document specifies a method to assess the disintegration of tissue paper and tissue products when subjected to mechanical agitation in water.

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This document specifies a method to assess the disintegration of tissue paper and tissue products when subjected to mechanical agitation in water.

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This document specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products after wetting.

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This document establishes general principles for the use of terms in the entire working field of tissue paper and tissue products.
It permits the use of a common terminology in industry and commerce.
It is expressly stated that ISO 15755 applies for the detection of impurities and contraries in tissue paper and tissue products.
For the determination of moisture content in tissue paper and tissue products, ISO 287 applies.

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This document specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products after wetting.

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This document establishes general principles for the use of terms in the entire working field of tissue paper and tissue products.
It permits the use of a common terminology in industry and commerce.
It is expressly stated that ISO 15755 applies for the detection of impurities and contraries in tissue paper and tissue products.
For the determination of moisture content in tissue paper and tissue products, ISO 287 applies.

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This document specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products after wetting.

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This document establishes general principles for the use of terms in the entire working field of tissue paper and tissue products. It permits the use of a common terminology in industry and commerce. It is expressly stated that ISO 15755 applies for the detection of impurities and contraries in tissue paper and tissue products. For the determination of moisture content in tissue paper and tissue products, ISO 287 applies.

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ISO 12625-6:2016 specifies a test method for the determination of grammage of tissue paper and tissue products.

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ISO 12625-6:2016 specifies a test method for the determination of grammage of tissue paper and tissue products.

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ISO 12625-6:2016 specifies a test method for the determination of grammage of tissue paper and tissue products.

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ISO 12625-9:2015 specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products.
Currently, two types of clamping devices are available on the market with two different diameters, one is with 50 mm and one is with 89 mm. ISO 12625-9:2015 applies for a 50 mm clamping device to be able to measure all sample sizes of tissue paper and tissue products and to be consistent with ISO 12625-11.

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ISO 12625-9:2015 specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products.
Currently, two types of clamping devices are available on the market with two different diameters, one is with 50 mm and one is with 89 mm. ISO 12625-9:2015 applies for a 50 mm clamping device to be able to measure all sample sizes of tissue paper and tissue products and to be consistent with ISO 12625-11.

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ISO 12625-9:2015 specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products. Currently, two types of clamping devices are available on the market with two different diameters, one is with 50 mm and one is with 89 mm. ISO 12625-9:2015 applies for a 50 mm clamping device to be able to measure all sample sizes of tissue paper and tissue products and to be consistent with ISO 12625-11.

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ISO 12625-3:2014 specifies a test method for the determination of thickness and bulking thickness and the calculation of apparent bulk density and bulk of tissue papers and tissue products under a pressure of 2,0 kPa.

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ISO 12625-3:2014 specifies a test method for the determination of thickness and bulking thickness and the calculation of apparent bulk density and bulk of tissue papers and tissue products under a pressure of 2,0 kPa.

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ISO 12625-3:2014 specifies a test method for the determination of thickness and bulking thickness and the calculation of apparent bulk density and bulk of tissue papers and tissue products under a pressure of 2,0 kPa.

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ISO 12625-8:2010 specifies a basket-immersion test method for the determination of water-absorption time and water-absorption capacity of tissue paper and tissue products.
It is expressly stated that the detection of impurities and contraries in tissue paper and tissue products be applied according to ISO 15755.
For the determination of moisture content in tissue paper and tissue products, ISO 287 is applicable.

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ISO 12625-8:2010 specifies a basket-immersion test method for the determination of water-absorption time and water-absorption capacity of tissue paper and tissue products.
It is expressly stated that the detection of impurities and contraries in tissue paper and tissue products be applied according to ISO 15755.
For the determination of moisture content in tissue paper and tissue products, ISO 287 is applicable.

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ISO 12625-8:2010 specifies a basket-immersion test method for the determination of water-absorption time and water-absorption capacity of tissue paper and tissue products. It is expressly stated that the detection of impurities and contraries in tissue paper and tissue products be applied according to ISO 15755. For the determination of moisture content in tissue paper and tissue products, ISO 287 is applicable.

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ISO 12625-5:2016 specifies a test method for the determination of the wet tensile strength of tissue paper and tissue products after soaking with water, using a tensile-strength-testing apparatus operating with a constant rate of elongation.
Currently, two types of tensile-strength-testing apparatus are commercially available, one where the test piece is positioned vertically and, for the other, horizontally. This document applies for both. For vertical tensile-strength-testing apparatus, a device which is held in the lower grip of the tensile-strength-testing apparatus, called a Finch Cup, is used to achieve the wetting. For horizontal tensile-strength-testing apparatus, the soaking device is placed between the clamps.
In cases where impurities and contraries have to be determined, ISO 15755[6] applies for these detections in tissue paper and tissue products.

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ISO 12625-4:2016 specifies a test method for the determination of the tensile strength, stretch at maximum force and tensile energy absorption of tissue paper and tissue products. It uses a tensile-testing apparatus operating with a constant rate of elongation.
It also specifies the method of calculating the tensile index and the tensile energy absorption index.
In cases where impurities and contraries have to be determined, ISO 15755[6] applies for these detections in tissue paper and tissue products.

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ISO 12625-15:2015 specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed in indoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions may be necessary.

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ISO 12625-16:2015 specifies the testing procedures for the instrumental determination of the opacity of tissue paper or tissue products by diffuse reflectance using a paper backing.
ISO 12625-16:2015 contains specific instructions for the preparation of test pieces of single-ply and multi-ply products, where special preparation/procedures might be necessary.
It can be used to determine the opacity of tissue paper and tissue products containing fluorescent whitening agents, provided the UV content of the radiation incident on the test piece has been adjusted to conform to that in the CIE illuminant C using a fluorescent reference standard provided by an authorized laboratory as described in ISO 2470-1.
ISO 12625-16:2015 is not applicable to coloured tissue paper and tissue products which incorporate fluorescent dyes or pigments.

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ISO 12625-7:2014 specifies testing procedures for the instrumental determination of brightness and colour of tissue paper and tissue products viewed under outdoor daylight conditions. It also gives specific instructions for the preparation of test pieces (single-ply, multi-ply products) and for the optical measurements of products, where special precautions may be necessary.

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ISO 12625-11:2012 specifies a test method for the determination of the resistance to mechanical penetration (ball burst strength procedure) of tissue paper and tissue products after wetting.

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ISO 12625-1:2011 establishes general principles for the use of terms in the entire working field of tissue paper and tissue products.
It permits the use of a common terminology in industry and commerce.

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ISO 12625-12:2010 specifies a test method for the determination of the tensile strength of perforated lines of tissue paper. It uses a tensile-testing apparatus operating with a constant rate of elongation.
This method is only used for measuring machine-direction tensile strength, that is for cross-direction perforations on tissue paper.
The calculation of perforation efficiency is also specified in ISO 12625-12:2010.

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ISO 12625-5:2016 specifies a test method for the determination of the wet tensile strength of tissue paper and tissue products after soaking with water, using a tensile-strength-testing apparatus operating with a constant rate of elongation.
Currently, two types of tensile-strength-testing apparatus are commercially available, one where the test piece is positioned vertically and, for the other, horizontally. This document applies for both. For vertical tensile-strength-testing apparatus, a device which is held in the lower grip of the tensile-strength-testing apparatus, called a Finch Cup, is used to achieve the wetting. For horizontal tensile-strength-testing apparatus, the soaking device is placed between the clamps.
In cases where impurities and contraries have to be determined, ISO 15755[6] applies for these detections in tissue paper and tissue products.

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    22 pages
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    e-Library read for
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