ISO 5636-5:2013
Current
Current
The latest, up-to-date edition.
Paper and board — Determination of air permeance (medium range) — Part 5: Gurley method
Available format(s)
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
Language(s)
English, French
Published date
10-17-2013
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ISO 5636-5:2013 specifies the Gurley method for determining the air permeance of paper and board using an air resistance tester, the Gurley apparatus.
It is applicable to papers and boards which have air permeances between 0,1 µm/(Pa⋅s) and 100 µm/(Pa⋅s) when tested with the Gurley apparatus.
It is unsuitable for rough-surfaced materials, which cannot be securely clamped to avoid leakage.
ISO 5636-5:2013 may also be used to determine the air resistance of paper and board.
| Committee |
ISO/TC 6/SC 2
|
| DevelopmentNote |
Supersedes ISO/FDIS 5636-5. (10/2013)
|
| DocumentType |
Standard
|
| Pages |
12
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| UNE-ISO 5636-5:2015 | Identical |
| BS ISO 5636-5:2013 | Identical |
| SS-ISO 5636-5:2013 | Identical |
| NF ISO 5636-5 : 2014 | Identical |
| NEN ISO 5636-5 : 2013 | Identical |
| UNI ISO 5636-5 : 2014 | Identical |
| 99/123128 DC : DRAFT SEP 99 | ISO/DIS 11607 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES |
| 17/30351717 DC : 0 | BS EN ISO 11607-1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| BS EN 60371-3-5:2006 | Insulating materials based on mica Specifications for individual materials - Glass-backed mica paper with an epoxy resin binder for post-impregnation (VPI) |
| ISO 11607-1:2006 | Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
| UNE-EN ISO 11607-1:2017 | Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006, including Amd 1:2014) |
| BS EN 60371-3-2:2006 | Insulating materials based on mica Specifications for individual materials - Mica paper |
| ASTM F 2981 : 2015 | Standard Test Method for Verifying Nonporous Flexible Barrier Material Resistance to the Passage of Air |
| BS EN ISO 5270:2012 | Pulps. Laboratory sheets. Determination of physical properties |
| EN 1086:1995 | Sacks for the transport of food aid - Recommendations on the selection of type of sack and the liner in relation to the product to be packed |
| BS EN ISO 11607-1:2017 | Packaging for terminally sterilized medical devices Requirements for materials, sterile barrier systems and packaging systems |
| CEI EN 60371-3-2 : 2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 2: MICA PAPER |
| NF EN ISO 11607-1 : 2018 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| UNE-EN ISO 5270:2013 | Pulps - Laboratory sheets - Determination of physical properties (ISO 5270:2012) |
| I.S. EN ISO 5270:2012 | PULPS - LABORATORY SHEETS - DETERMINATION OF PHYSICAL PROPERTIES (ISO 5270:2012) |
| I.S. EN ISO 15882:2008 | STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
| ONORM EN ISO 5270 : 2013 | PULPS - LABORATORY SHEETS - DETERMINATION OF PHYSICAL PROPERTIES (ISO 5270:2012) |
| BS ISO 5636-6:2015 | Paper and board. Determination of air permeance (medium range) Oken method |
| 14/30255135 DC : 0 | BS EN ISO 11607-1:2009/A1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| DIN EN ISO 11607-1:2014-11 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS (ISO 11607-1:2006 + AMD 1.:2014) |
| I.S. EN 60371-3-5:2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 5: GLASS-BACKED MICA PAPER WITH AN EPOXY RESIN BINDER FOR POST-IMPREGNATION (VPI) |
| AAMI ISO 15882 : 2008 | STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
| CSA Z15882:09 (R2019) | Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (Adopted ISO 15882:2008, second edition, 2008-09-01) |
| NF EN 60371 3-2 : 2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 2: MICA PAPER |
| I.S. EN 60371-3-2:2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 2: MICA PAPER |
| UNI EN ISO 5270 : 2012 | PULPS - LABORATORY SHEETS - DETERMINATION OF PHYSICAL PROPERTIES |
| UNI EN ISO 15882 : 2009 | STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
| CSA ISO 11607-1 : 2016 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| ASTM D 2068 : 2017 : REDLINE | Standard Test Method for Determining Filter Blocking Tendency |
| ISO 11607:2003 | Packaging for terminally sterilized medical devices |
| BS ISO 5270:1998 | Pulps. Laboratory sheets. Determination of physical properties |
| IP PM ES : 2016 | DETERMINATION OF COLD FILTER BLOCKING TENDENCY |
| UNI EN ISO 11607-1 : 2014 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| ISO 5636-6:2015 | Paper and board Determination of air permeance (medium range) Part 6: Oken method |
| EN 60371-3-2:2006/corrigendum:2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 2: MICA PAPER |
| EN 60371-3-5 : 2006 COR 2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 5: GLASS-BACKED MICA PAPER WITH AN EPOXY RESIN BINDER FOR POST-IMPREGNATION (VPI) |
| BS EN ISO 11607-1:2020 | Packaging for terminally sterilized medical devices Requirements for materials, sterile barrier systems and packaging systems |
| DIN EN ISO 5270:2013-02 | Pulps - Laboratory sheets - Determination of physical properties (ISO 5270:2012) |
| ANSI/AAMI/ISO 15882:2008(R2013) | STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
| IEC 60371-3-2:2005 | Insulating materials based on mica - Part 3: Specifications for individual materials - Sheet 2: Mica paper |
| IEC 60371-3-5:2005 | Insulating materials based on mica - Part 3: Specifications for individual materials - Sheet 5: Glass-backed mica paper with an epoxy resin binder for post-impregnation (VPI) |
| ISO 5270:2012 | Pulps — Laboratory sheets — Determination of physical properties |
| BS EN ISO 15882:2008 | Sterilization of health care products. Chemical indicators. Guidance for selection, use and interpretation of results |
| EN ISO 5270:2012 | Pulps - Laboratory sheets - Determination of physical properties (ISO 5270:2012) |
| EN ISO 15882:2008 | Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO 15882:2008) |
| CSA Z15882 : 2009 : R2014 | STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
| 14/30219261 DC : 0 | BS ISO 5636-6 - PAPER AND BOARD - DETERMINATION OF AIR PERMEANCE AND AIR RESISTANCE (MEDIUM RANGE) - PART 6: OKEN METHOD |
| CSA Z15882 :2009 | STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
| CEI EN 60371-3-5 : 2006 | INSULATING MATERIALS BASED ON MICA - PART 3: SPECIFICATIONS FOR INDIVIDUAL MATERIALS - SHEET 5: GLASS-BACKED MICA PAPER WITH AN EPOXY RESIN BINDER FOR POST-IMPREGNATION (VPI) |
| TAPPI T 460 : 2011 | AIR RESISTANCE OF PAPER (GURLEY METHOD) |
| 04/30101211 DC : DRAFT APR 2004 | ISO 11607-1 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| I.S. EN ISO 11607-1:2017 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS (ISO 11607-1:2006, INCLUDING AMD 1:2014) |
| ASTM F 2097 : 2016 : REDLINE | Standard Guide for Design and Evaluation of Primary Flexible Packaging for Medical Products |
| BS EN ISO 11607-1 : 2009 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| ISO 15882:2008 | Sterilization of health care products — Chemical indicators — Guidance for selection, use and interpretation of results |
| BS EN 868-1:1997 | Packaging materials and systems for medical devices which are to be sterilized General requirements and test methods |
| ISO 5725-1:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions |
| ISO 385:2005 | Laboratory glassware — Burettes |
| ISO 187:1990 | Paper, board and pulps — Standard atmosphere for conditioning and testing and procedure for monitoring the atmosphere and conditioning of samples |
| ISO/TR 24498:2006 | Paper, board and pulps Estimation of uncertainty for test methods |
| ISO 186:2002 | Paper and board — Sampling to determine average quality |
| ISO 48:2010 | Rubber, vulcanized or thermoplastic Determination of hardness (hardness between 10 IRHD and 100 IRHD) |
| TAPPI T 1200 : 2014 | INTERLABORATORY EVALUATION OF TEST METHODS TO DETERMINE TAPPI REPEATABILITY AND REPRODUCIBILITY |
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