ASTM D4178-1982(2012) Standard Practice for Calibrating Moisture Analyzers《湿度分析仪校准的标准实施规程》.pdf
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1、Designation: D4178 82 (Reapproved 2012)Standard Practice forCalibrating Moisture Analyzers1This standard is issued under the fixed designation D4178; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A numb
2、er in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This practice covers a calibration technique based on thepreparation of standards of known water content. This tech-nique is applicable to
3、the production of standards between 20and 2000 cm3/m3water.1.2 The values stated in SI units are to be regarded asstandard. The values given in parentheses are for informationonly.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is therespo
4、nsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Summary of Practice22.1 The practice is based on the principle that ice has avapor pressure of 0.611 kPa at 0C. Therefore, when a ca
5、rriergas at a constant gauge pressure of 207 kPa (30 psig) is passedthrough a molecular sieve saturated with water and held at 0C,the total pressure is equal to 207 kPa plus 98 kPa (oneatmosphere) and the water concentration of the gas leaving themolecular sieve is 0.611/(207 + 98) 3 106ppm or 2000
6、ppmvolume water, regardless of flow.2.1.1 A carrier gas at a constant gauge pressure of 207 kPais passed through a molecular sieve drier and then routed overa molecular sieve support saturated with water and equilibratedat 0C.2.1.2 By blending different volumes of the wet carrier gaswith dried carri
7、er gas, gas standards of known water concen-tration can be prepared.2.2 The moisture analyzer to be calibrated is then connectedto the source of the gas standard of known water concentration.3. Significance and Use3.1 This practice is intended to provide a method to cali-brate moisture analyzers use
8、d on-stream or in the laboratory.4. Apparatus4.1 Ice Bath Primary Standard Moisture ApparatusFig. 1illustrates a typical system.4.2 Wet Test Meter, 1-L divisions.4.3 Bubble Meter, graduated in cubic centimetres.4.4 Pressure GaugeA Bourdon-type spring gauge of testgauge quality, 100 to 250 mm in diam
9、eter, with a scale rangefrom 0 to 400 kPa (0 to 60 psi), maximum intermediategraduations of 1.5 kPa (0.25 psi).4.5 Wet Mole Sieve 5A, 60/80 mesh (other mesh sizes maybe used, except powder).5. Preparation of Apparatus5.1 Saturate mole sieve with water.5.1.1 Cover in beaker enough mole sieve to fill
10、the wet molesieve container. Add water to cover mole sieve. Let standovernight.5.1.2 Drain the excess water by pouring the mole sieveslurry into a filtering funnel and letting all the free water drainout.NOTE 1The useful lifetime of the wet mole sieve is not known. It isrecommended that the procedur
11、e described in 5.1.1 and 5.1.2 be followedprior to each calibration.6. Procedure6.1 Fill the ice bath bucket for the primary standard appa-ratus one third full of water; then add ice to bring the level tofull.6.2 Close the wet flow and the diluent flow needle values.6.3 Turn on the carrier gas suppl
12、y (nitrogen or air) andadjust the regulator to 207 kPa (30 psig).6.4 Open the diluent flow needle valve to obtain a carriergas flow of 1 L/min, as measured with a wet test meter.6.5 Allow the apparatus to equilibrate for 1 h. This allowsthe wet mole sieve to equilibrate at 0C.6.6 After 1 h, attach t
13、he moisture analyzer to be calibratedand check that the blank moisture content of the carrier gas is6 ppm or less.1This practice is under the jurisdiction of ASTM Committee D02 on PetroleumProducts and Lubricants and is the direct responsibility of Subcommittee D02.D0 onHydrocarbons for Chemical and
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