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Ts en 12572 - Su Buharı

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296 views34 pages

Ts en 12572 - Su Buharı

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Kemal Yücel
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TURK STANDARDI TURKISH STANDARD BINALARDA KULLANILAN MALZEMELERIN VE ORUNLERIN HIGROTERMAL PERFORMANSI- SU BUHARI AKTARIMI OZELLIKLERININ BELIRLENMESi Hygrothermal performance of building materials and products - Determination of water vapour transmission properties (ISO 12572:2001) See TURK STANDARDLARI ENSTITUSU Necatibey Caddesi No.112 Bakanliklar/ANKARA TORK STANDARDI Gn séz ~ Bu standard, Tark Standardlan Enstitisd tarafindan ilgili Avrupa standardi esas almarak TOrk Standart olarak kabul edilmistr, EUROPEAN STANDARD EN ISO 12572 NORME EUROPEENNE EUROPAISCHE NORM June 2004 Ics 91,120.10 English version Hygrothermal performance of building materials and products - Determination of water vapour transmission properties (ISO 12572:2001) Pesfornance hysrathoriqus des matérix produits \Worrne- und Icuchistechniaches Verhaitan won Baustfien ‘our le Boument- Determination des propricies de ‘ne Boupraduten = estremng Ger ansriszon cols vapeur d'eau (190 125727001) \Weaseerdarrptdurchiacalgkat (1&0 12572 2001) ‘This European Standard was aporowet by CEN on 18 October 2900, CEN mombare are bound te cere With hs CERICENELEC Internat Regulation which atipuate the condions for ving this European Standard the slatus of national standard without any ateraten, Up-to-date tite and bbllogaphical elerences concening such nation Sanda may be dbtained on applcalan to the Managemert Cente orto any CEN maeber ‘This European Stancard exist in three offcial versions (Engich, French, German). Aversion many aihar language made by tanslstion Under tha rasponsibity of & CEN member ita its ows language ard nothed tothe Management Cente has the sarne fais asthe ofa] CEN members ar the national standards badiae of Ausia, Belgum, Czech Republic, Qerimirk, Finiand, France, Geman, Gres, leelanc, lela, Maly, Lucerdaug, Netherlands, Norway, Pongal, Spain, Sweden, Sht2erland and Unilae! Kingdon a— | ECROPEAN COMMATTTER FOR STANDARUEZTION COMITE EUROPEEN DE WORBALISATION ELKOPAISCHES KOMITEE FLX NOR MUNG Management Gente: rua de Stassntt, 36 B-10S0 Brussels ©2001 CEN Allights of exploation in any form and by any'rmsans rasanved Rot. No. EM Iso. 12572-2001 F ‘werldwisa for CEN national Maribers. Page 2 EIN ISO 12572:2001 Contents Foreword 1 Scope 2 Normative references 3 Definitions, symbols and units 4 Principle 5 Apparatus 6 Test specimens 7 Procedure 8 Calculation and expression of results 9 Accuracy of measurement 10 Test report Annex.A (normative) Methods suitable for self supporting macerials Annex B (normative) Methods suitable for loose fills ‘Annex C (normative) Methods suitable for membranes and foils Annex D (normative) Methods suitable for mastics and sealants Annex E (normative) Methods suitable for paint, varnishéa, ete Annex F (normative) Correction for the effect of a masked edge of a specimen Annex G (normative) Correction for resistance of air layers Annex H (informative) Weighing repeatability, weighing interval and specimen size needed to achieve desired accuracy Annex J (informative) Conversion table for water vapour transmission units ANNEX ZA (normative) Normative references te international publications with their relevant European publications uM ANNEX ZB (informative) Informative references to inteational publications with their i w Bibliography q Page 3 ENISO 12572:2001 Foreword The text of EN ISO 12572:2001 has been prepared by Technical Committee CEN/TC 89 “Thermal performance of buildings and building components", the secretariat of which is held by SIS, in collaboration with Technical Committee ISO/TC 163 "Therimal insulation”, ‘This European Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by December 2001, and conflicting national standards shall be withdrawn at the latest by December 2001. ‘This standard is one of a series of standards which specify test methods for the thermal and moisture related properties of building materials and products. ‘The European publications to be used instead of the International Standards listed in clause 2 are given in normative annex ZA, which is an integral part of this European Standard, The annexes A, B, C, D; E, F, Gand 2A are normative. The annexes H, J and ZB are informative. According to the CEN/CENELEC intemal Regulations, the national standards organizations of the following countries arc bound te implement this European Standard: Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland and the United Kingdom, Page 4 EN ISO 12572:2001 1 Scope ‘This standard specifies a method based on cup tests for determining the water vapour permeance of building products and the water vapour permeability of building materials under isothermal conditions. Different sets of test conditions are specified. ‘The general principles are applicable 1o all hygroscopic and non hygroscopic building materials and products, including those with facings and integral skins. Annexes give details of test methods suitable for different material types. This standard is not applicable in the ccase of test specimens with water vapour diffusion-equivalent air layer thickness values less than 0.1 m, as a result of increasing uncertainty in the measurement results. If the measured ‘water vapour diffusion-cquivalent air fayer thickness is greater than 1500 m the material can bbe considered impermeable. ‘The results obtained by this method are suitable for design purposes, production control and for inclusion in product specifications, 2 Normative references This European Standard incorporates by dated or undated reference, provisions from other publications. These normative references are cited at the appropriate places in the text and the publications are listed hereafter. For dated references, subsequent amendments to or revisions of any of these publications apply to this European standard only when incorporated in it by amendment or revision, For undated references the latest edition of the publication referred t0 applies (including amendments) 180.9346 Thermal insulation - Mass transfer - Physical quantities and definitions Page 5 EN ISO 12572:2001 3 Definitions, symbols and units 3.1 Terms and definitions For the purposes of this standard, the terms and definitions given in ISO. 9346 and the following apply. al density of water vapour flow rate ‘mass of water vapour transferred through the specimen pet area and per time 312 homogeneous material material with properties likely to affect the transmission of water vapour which do not vary on a macroscopic scale 3.13 water vapour permeance density of water vapour flow rate divided by the water vapour pressure difference between the two specimen faces B14 water vapour resistance reciprocal of water vapour permeance 21s water vapour permeability product of the water vapour permeance and the thickness of a homogencous specimen NOTE Water vapour permeability can only be calculated for specimens of a homogeneous material B16 water vapour resistance factor ‘water vapour permeability of air divided by that of the material concemed NOTE. The water vapour resistance factor indicates haw much greater the resistance of the material is compared to an equally thick laycr of stationary air at the same temperature. 3.17 water vapour diffusion-equivalent air layer thickness thickness ofa motionless air layer which has the same water vapour resistance as the specimen Page 6 EN ISO 12572:2001 3.2 Symbols and units Symbol_| Quantity Unit ‘4 | arca of specimen mm G —_| water vapour flow rate through specimen kp’s R, | gas constant for water vapour = 462 NeawikeK) S| hydraulic diameter of specimen m T | thermodynamic temperature K W, | water vapour permeance with respect to partial kg'(m?-s Pa) vapour pressure Z, —_| water vapour resistance with respect to partial ms Parke vapour pressure D_—_| mean thickness of specimen m g | density of water vapour flow rate kgm?) t diameter of circle or side of square specimen m m | mass.of specimen and cup assembly ke. p | barometric pressure hPa po _| standard barometric pressure= 1013,25 hPa $4 | water vapour diffusion-equivalent air layer m thickness t time s Spw | water vapour pressure difference across specimen | Pa & _| water vapour permeability with respect to partial | kg/(m-s'Pa) ‘vapour pressure 6, | water vapour permeability of air with respect to —_| kg/(m-s-Pa) partial vapour pressure | water vapour resistance factor - @ Celsius temperature *c relative humidit ‘NOTE The above units comply with ISO 9346; a conversion table to other units ‘commonly used in permeability measurements is given in annex J. 3. Subscripts Subscript _| Denoting 1 interval repeatability air ‘corrected for ait layer r a c f rr Ee Page? EN ISO 12572:2001 4 Principle ‘The test specimen is sealed to the open side of a test cup coniaining cither a desiccant (dry -cup) or an aqueous saturated solution (wet cup), The assembly is then placed in a temperature and humidity controlled test chamber. Becanse af the different partial vapour pressure between the test cup and the chamber, a vapour flow occurs through permeable specimens Periodic weighings of the assembly are made to determine the rate of water vapour ‘transmission in the steady state. 5 Apparatus a) Test cups resistant to corrosion from the desiccant or salt solutions they contains typically cups are made of glass or metal. ‘The design of cups suitable for testing various different types of materials is described in annexes A to E, NOTE. Circular cups can be easier to seal and transparent cups allow better control of salt solutions, b) For certain cups and sealing methods (see annex A), a template, with shape and size corresponding to that of the test cup, is used when applying the sealant to give a sharply defined, reproducible test arca, The template shall have an arca of at least 90 % of the specimen to limit non-linear vapour flow. ©) Measuring instruments capable of determining specimen thickness with accuracy required in 7.2. 4) Analytical balance, capable of weighing the test assembly with the repeatability needed for the required accuracy. Wherever possible a balance of 0,001 g resolution shall be used. For heavy test assemblies a balance resolution of 0,01 g may be sufficient. Sce annex H for information linking the balance resolution to the duration of test. NOTE The factors that affect the necessary accuracy of measurement are discussed in annex H. ©) Constant temperature, constant humidity chamber, capable of being maintained within £3 % relative humidity around the sct point relative humidity and + 0,5 K around the set point temperature. In order to ensure uniform conditions throughout the chamber, the air shall be stirred so as to obtain velocities between 0,02 mvs and 0,3 mvs. If highly permeable materials are being tested, means should be provided to measure the air peed directly over the upper surface of the specimen - sce annex G. 1) Suitable sensors and a logging system to continuously record the temperature, relative humidity and, if necessary, the barometric pressure within the test chamber. The sensors shall be calibrated at regular intervals. Pave 8 EN ISO 12572-2001 1) Sealant, which is impermeable to water vapour, does noc undergo physical or chemical changes during the test and docs not cause physical or chemical changes to the specimen. NOTE Examples of sealants suitable for specific materials, if necessary, are listed in the appropriate annex. 6 Test specimens 6.1 General principles for preparation of test specimens The test specimens shall be representative of the product. If the product has natural skins or integral facings, these may bc included in the test specimen, but they shall be temoved if itis intended to measure the permeability of the core material, Ifthe skins or facings ate different on the two sides, specimens shall be tested with vapour flow in the direction of the intended use. Ifthe direction of flow is not known, duplicate specimens shall he prepared and tests carried out for each direction of flow. Unless the product to be tested in isotropic, the test specimens shall be cut so that the parallel faces are normal to the direction of vapour flow of the product in use. Specimen preparation shall not involve methods which damage the surface in ways which Affect the flow of water vapour. 6.2 Dimensions of test specimens 6.2.1 Shape and fit ‘Test specimens shall be cut to correspond with the dimensions of the chosen test assembly ~ see annexes A to E. 6.22 Exposed area ‘The diameter of a circular specimen or the side of a square specimen shall be at least twice the specimen thickness, The exposed area (the arithmetic mean of the upper and lower free surface arcas} shall be at least 0,005 m*. The upper and lower free surface ateas shall not differ by more than 3 % of the mean in the case of homogencous materials, and by no more than 10 % in the case of other materials. 6.2.3 Thickness of test specimens. ‘Whenever possible, the thickness of the specimen shall be that of the product in use. In the case of homogeneous materials, if the thickness exceeds 100 mm, this may be reduced by cutting, In the case of non homogencous materials, such as concrete containing aggregates, the thickness should be at least three times (and preferably five times) the largest particle size, ‘If.a material contains macroscopic formed voids, the solid material should be (ested and the resistance of the whole material calculated from the proportions of solid to air space assuming ‘one dimensional vapour flow. Page? EN ISO 12572-2001 IF it is necessary to test a product so thick that the available test cups do not have an area lange enough to comply with 6.2.2, the product may, only as a last resort, be sliced. In this case, all slices shall be tested and the resulls reported. NOTE This procedure may lead to significant inaccuracies, especially when wet cup ests are carried out on hygroscopic materials. 6.3 Number of iest specimens Ifthe specimen area is fess than 0,02 m3, a minimum of five specimens shall be tested, otherwise a minimum of three specimens shall be tested. 64 Conditioning of test specimens Before testing, the test specimens shall be stored at (23 4 5) °C, (50+ 5) % relative humidity for a pesiod long enough for their weight to stabilise so thal three successive daily determinations of their weight agree to within 5 %. NOTE This period will vary from a few hours in the case of some insulating materials to 3-4 weeks of more for massive hygroscopic materials and products, Wet field specimens may be dried before conditioning using the methods specified in 180 12570, Hygrothermal performance of building materials and products ~ Determination of moisture content by drying at elevated temperature. A period of conditioning is not necessary in the ease of plastic membranes. Page 10 IBN ISQ 12572:2001 7 Procedure 7.1 Test conditions ‘Select the desired test environment from the sets of conditions given in Table 1. ‘Table Il - Test com jons Condition Relative humidity °C-%RH “6 % Dry state Wet slate ‘Set point | Tolerance | Sex point | Tolerance A_| 23-050. 23£05 o +3 50 a3 B | 23-0785 23205 o +3 85 +3 © | 33-5003 2205 +3 93 +3 D_| 38-093 3805 +3 93 +3 NOTE | ‘Dry cup’ tests (condition A) give information about the performance of materials at low humidities when moisture transfer is dominated by vapour difTusion “Wet cup” tests (condition C) give guidance about the performance of materials under high humidity conditions, At higher humidities, the material pores start to fill with ‘water; this increases the transport of liquid water and reduces vapour transport, Tests in this area therefore give some information about liquid water transport within materials. This is discussed further in ISO 15148, Hygrothermal performance of building materials and products - Determination of water absorption coefficient by partial immersion. Other sets of temperature and relative humidity may be agroed between the parties when needed for special application conditions. NOTE 2 The following are examples of desiccants and saturated aqueous solutions which produce the specified air relative humidities at 23 °C: a) Desiceants Calcium chloride, CaCl - particle size <3 mm 0% Magnesium perchlorate, Mg(C10.):) 0% b) Aqueous solutions Magnesium nitrate, Mg(NO3}2 53% Potassium chloride, KCL 85% Ammonium dihydrogen phosphate, NIILPOs 93 % Page 11 EN ISO 12572:2001 Potassium nitrate, KNO3 94% Further details of suitable solutions can be found in annexes A and B of ISO 12571, Lygrothermal performance of building materials and products - Determination of hygroscopic sorption curves, Regular checks shall be made, especially during long tests, to ensure that aturated solutions remain as a mixture of liquid with a large amount of undissolved substance All chemical substances shall be handled with cate and in accordance with relevant safety regulations. 7.2 Preparation of specimen and test assembly Prepare test spocimens to correspond to the test assembly used - see annexes A to E, Mcasure the thickness of specimens to the nearest 0,1 fini, oF to an accuracy of = 0.5 %, whichever is the more accurate, For rigid materials, measure the thickness of test specimens at four positions equally spaced around the circumference. Calculate the mean thickness of cach test specimen. Record the procedure used to measure the effective thickness of compressible and loose-fill materials and of test specimens with irregular surfaces. Place the desiccant or aqueous solution, with a minimum depth of 15 mm in the bottom of cach cup. Scal the fest specimen into the cup, using the appropriate technique specified in the relevani annex, ‘The air space between the desiccant or saturated solution and the specimen shall be (15 5) mm, Prepare a test assembly using a cup and sealant system suitable for the type of matcrial under test - see annexes A to E. 7.3 Test procedure weighing procedure. NOTE Annex H gives guidance on the ways of reaching the required accuracy. Weighings shall be carried out in an environment with a temperature within = 2 °C of the test condition, wherever possible within the test chamber, Figure | shows an arrangement for small chambers. ‘The temperature and relative humidity within the test chamber shall be recorded continuously with suitable sensors, The calibration of the sensors shall be checked regularly. Page 12 EN ISO 12572:2001 ‘The barometric pressure at the testing laboratory shall be measured daily during the test: obtained from a closely adjacent meteorological station. Key 1 Balance 2 Controlled environment test chamber with ‘glove box’ access door 3° Suspended weighing platform 4 Test assembly during weighing Figure 1 - Example of an arrangement of balance and test assemblies for weighing procedures in a chamber Continue weighings until five successive determinations of change in mass per weighing interval for each test specimen are constant within + 5 % of the mean value for this specimen (or within 10 % for low permeance materials with > 750 000) and until the change in weight of the cup assembly exceeds 100 times the repeatability of the weighing procedure. Plot a curve of change in mass against time to facilitate recognition of the condition of constant mass change rate. The test shall be terminated prematurely when: i) ina dry cup test, the assembly has gained more that 1,5 g per 25 ml of desiccant in the cup; ii) in a wet cup test, the weight loss is half the initial mass of the solution in the cup. Page 13 EN ISO 12572:2001 8 Calculation and expression of results 8.1 Mass change rate For each set of successive weighings of the specimens, calculate the mass change rate, Avis, using : vin a toh where Ara is the change of mass per time for a single determination, in kg/s; m is the mass of the test assembly at time 4, in kg; m is the mass of the test assembly at time 2, in kg; fyandf, —_are the successive times of weighings, in s. Calculate the regression line between mass and time, excluding the earlier, non-linear, stage of the test, The slope of this line is G, in kg/s NOTE If required, the standard error of the slope of the regression line (i.e. the standard error of the flow rate) can be found by standard statistical methods. 8.2 Density of water vapour flow rate The density of water vapour flow rate, g, is given by: nce 7 Q) where A is the exposed area (arithmetic mean of the free upper and free lower surface areas) of the test specimen, in m’. Ifa cup and sealant system which includes a ‘masked edge’ (see annex A) has been used, values shall be corrected before being used to calculate further parameters - see annex F. 8.3 Water vapour permeance ‘The water vapour permeance, W, is given by : G A-dp, 8) The value of Apy shall be calculated from the mean of the measured temperature and relative humidity over the course of the test. Page 14 EN ISO 12572:2001 NOTE For temperatures greater than 0 °C, the vapour pressure on either side of the specimen may be calculated from the temperature and relative humidity using (see reference [11] in the Bibliography): 172696 Pea = 96105-6777 If highly permeable materials or thin membranes, with ss < 0,2 m, are being tested, the resistance of the air gap between the base of the sample and the desiccant or saturated solution shall be taken into account in the calculation of W’- see annex G. 8.4 Water vapour resistance The water vapour resistance, Z, is the reciprocal of the water vapour permeance: 1 @) 8.5 Water vapour permeability The water vapour permeability, , is given by: b=Wed 6) 8.6 Water vapour resistance factor The water vapour resistance factor, is defined by the equation : 5, a 6) _ © Equation (7), known as the Schirmer formula, is used to calculate 6,, using the mean barometric pressure, p, over the test. i 5, = Po (S o R,-T-p\273 Values of 6; at 23 °C are shown in Figure 2. The water vapour permeability of air and the material may be assumed to vary equally with the barometric pressure. The factor 17 can therefore be considered independent of barometric. pressure. When calculating the density of water vapour flow rate using the expression : @) the value of 6, shall correspond to the actual barometric pressure. Page 15 EN ISO 12572:2001 ‘Vapour permeability 10'° kg/(m.s.Pa) 24 22 20 18 —— 800 850 00 950 1000 1050 1100 pe Darometric Pressure Figure 2 - Water vapour permeability of air as a function of barometric pressure at 23°C 8.7 Water vapour diffusion-equivalent air layer thickness ‘The water vapour diffusion-equivalent air layer thickness, sa, is given by either: wed (9a) sa= OeZ (9b) 9 Accuracy of measurement 9.1 General This clause and annex H discuss the factors that affect the accuracy of the result and give guidance how to improve it, if necessary. NOTE A number of ‘round-robin’ intercomparisons of measurements by different laboratories have been carried out - see references [6], [7] and [8] in the Bibliography for discussion of the results. A number of factors affect the accuracy of the measured values. 9.2 Specimen area The diameter of a circular test cup or the side of a square test cup shall be measured to an accuracy of + 0,5 mm, giving a possible error in the area of a specimen of the minimum size specified in 6.2.2 (i.e. 0,005 m2) of +0,5 %. This error will be less with larger specimens. For certain cup types it will be necessary to correct for the effect of a masked edge as specified in annex F. Page 16 EN ISO 12572:2001 9.3 Specimen thickness If the permeance or resistance of a complete product is being measured, the accuracy is affected by the thickness. However if the permeability of a material is needed, the with which the specimen thickness can be measured will directly effect the accuracy of result. The thickness of a rigid specimen can be measured to better than 0,5 % with a micrometer. NOTE The accuracy will be lower in the case of loose fill and similar materials. 9.4 Sealants If an appropriate sealant is installed as specified in the annexes, errors caused by leakage: ‘be much less than those from other sources. A faulty seal will result in a much higher flow rate through one of the test assemblies; that result shall be rejected before averages are over the samples. 9.5 Weighing precision The influence of weighing uncertainty on the accuracy of the results depends on the size off specimen and the time interval between successive weighings. NOTE Information about the weighing repeatability needed to achieve a desired accuracy in relation to the specimen size and weighing interval is given in annex H. 9.6 Control of environmental conditions The vapour pressure difference between the test cup and the environmental chamber is the

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