ASTM D445-2010 Standard Test Method for Kinematic Viscosity of Transparent and Opaque Liquids (and Calculation of Dynamic Viscosity)《透明和不透明液体运动粘度的标准试验方法(包括动态粘度的计算)》.pdf

《ASTM D445-2010 Standard Test Method for Kinematic Viscosity of Transparent and Opaque Liquids (and Calculation of Dynamic Viscosity)《透明和不透明液体运动粘度的标准试验方法(包括动态粘度的计算)》.pdf》由会员分享，可在线阅读，更多相关《ASTM D445-2010 Standard Test Method for Kinematic Viscosity of Transparent and Opaque Liquids (and Calculation of Dynamic Viscosity)《透明和不透明液体运动粘度的标准试验方法(包括动态粘度的计算)》.pdf（11页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D445 10Designation: 71/1/97British Standard 2000: Part 71:1990Standard Test Method forKinematic Viscosity of Transparent and Opaque Liquids(and Calculation of Dynamic Viscosity)1This standard is issued under the fixed designation D445; the number immediately following the designation in

2、dicates the year oforiginal adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies

3、of the Department of Defense.1. Scope*1.1 This test method specifies a procedure for the determi-nation of the kinematic viscosity, n, of liquid petroleumproducts, both transparent and opaque, by measuring the timefor a volume of liquid to flow under gravity through acalibrated glass capillary visco

4、meter. The dynamic viscosity, h,can be obtained by multiplying the kinematic viscosity, n,bythe density, r, of the liquid.NOTE 1For the measurement of the kinematic viscosity and viscosityof bitumens, see also Test Methods D2170 and D2171.NOTE 2ISO 3104 corresponds to Test Method D445.1.2 The result

5、 obtained from this test method is dependentupon the behavior of the sample and is intended for applicationto liquids for which primarily the shear stress and shear ratesare proportional (Newtonian flow behavior). If, however, theviscosity varies significantly with the rate of shear, differentresult

6、s may be obtained from viscometers of different capillarydiameters. The procedure and precision values for residual fueloils, which under some conditions exhibit non-Newtonianbehavior, have been included.1.3 The range of kinematic viscosities covered by this testmethod is from 0.2 to 300 000 mm2/s (

7、see Table A1.1)atalltemperatures (see 6.3 and 6.4). The precision has only beendetermined for those materials, kinematic viscosity ranges andtemperatures as shown in the footnotes to the precision section.1.4 The values stated in SI units are to be regarded asstandard. The SI unit used in this test

8、method for kinematicviscosity is mm2/s, and the SI unit used in this test method fordynamic viscosity is mPas. For user reference, 1 mm2/s=10-6m2/s = 1 cSt and 1 mPas=1cP=0.001 Pas.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresp

9、onsibility 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. Referenced Documents2.1 ASTM Standards:2D446 Specifications and Operating Instructions for GlassCapillary Kinematic ViscometersD119

10、3 Specification for Reagent WaterD1217 Test Method for Density and Relative Density (Spe-cific Gravity) of Liquids by Bingham PycnometerD1480 Test Method for Density and Relative Density (Spe-cific Gravity) of Viscous Materials by Bingham Pycnom-eterD1481 Test Method for Density and Relative Density

11、 (Spe-cific Gravity) of Viscous Materials by Lipkin BicapillaryPycnometerD2162 Practice for Basic Calibration of Master Viscometersand Viscosity Oil StandardsD2170 Test Method for Kinematic Viscosity of Asphalts(Bitumens)D2171 Test Method for Viscosity of Asphalts by VacuumCapillary ViscometerD6071

12、Test Method for Low Level Sodium in High PurityWater by Graphite Furnace Atomic Absorption Spectros-copyD6074 Guide for Characterizing Hydrocarbon LubricantBase OilsD6299 Practice for Applying Statistical Quality Assuranceand Control Charting Techniques to Evaluate AnalyticalMeasurement System Perfo

13、rmanceD6617 Practice for Laboratory Bias Detection Using Single1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.07 on Flow Properties.Current edition approved Oct. 1, 2010. Published November 201

14、0. Originallyapproved in 1937. Last previous edition approved in 2009 as D44509. DOI:10.1520/D0445-10.In the IP, this test method is under the jurisdiction of the StandardizationCommittee.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at service

15、astm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1*A Summary of Changes section appears at the end of this standard.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United

16、 States.Test Result from Standard MaterialE1 Specification for ASTM Liquid-in-Glass ThermometersE77 Test Method for Inspection and Verification of Ther-mometers2.2 ISO Standards:3ISO 3104 Petroleum ProductsTransparent and OpaqueLiquidsDetermination of Kinematic Viscosity and Cal-culation of Dynamic

17、ViscosityISO 3105 Glass Capillary Kinematic ViscometersSpecification and Operating InstructionsISO 3696 Water for Analytical Laboratory UseSpecification and Test MethodsISO 5725 Accuracy (trueness and precision) of measure-ment methods and results.ISO 9000 Quality Management and Quality AssuranceSta

18、ndardsGuidelines for Selection and UseISO 17025 General Requirements for the Competence ofTesting and Calibration Laboratories2.3 NIST Standards:4NIST Technical Note 1297 Guideline for Evaluating andExpressing the Uncertainty of NIST Measurement ResultsNIST GMP 11NIST Special Publication 8193. Termi

19、nology3.1 Definitions of Terms Specific to This Standard:3.1.1 automated viscometer, napparatus which, in part orin whole, has mechanized one or more of the procedural stepsindicated in Section 11 or 12 without changing the principle ortechnique of the basic manual apparatus. The essential ele-ments

20、 of the apparatus in respect to dimensions, design, andoperational characteristics are the same as those of the manualmethod.3.1.1.1 DiscussionAutomated viscometers have the capa-bility to mimic some operation of the test method whilereducing or removing the need for manual intervention orinterpreta

21、tion. Apparatus which determine kinematic viscosityby physical techniques that are different than those used in thistest method are not considered to be Automated Viscometers.3.1.2 density, nthe mass per unit volume of a substance ata given temperature.3.1.3 dynamic viscosity, nthe ratio between the

22、 appliedshear stress and rate of shear of a liquid.3.1.3.1 DiscussionIt is sometimes called the coefficient ofdynamic viscosity or, simply, viscosity. Thus dynamic viscos-ity is a measure of the resistance to flow or deformation of aliquid.3.1.3.2 DiscussionThe term dynamic viscosity can alsobe used

23、 in a different context to denote a frequency-dependentquantity in which shear stress and shear rate have a sinusodialtime dependence.3.1.4 kinematic viscosity, nthe resistance to flow of a fluidunder gravity.3.1.4.1 DiscussionFor gravity flow under a given hydro-static head, the pressure head of a

24、liquid is proportional to itsdensity, r. For any particular viscometer, the time of flow of afixed volume of fluid is directly proportional to its kinematicviscosity, n, where n = h/r, and h is the dynamic viscositycoefficient.4. Summary of Test Method4.1 The time is measured for a fixed volume of l

25、iquid toflow under gravity through the capillary of a calibratedviscometer under a reproducible driving head and at a closelycontrolled and known temperature. The kinematic viscosity(determined value) is the product of the measured flow timeand the calibration constant of the viscometer. Two suchdet

26、erminations are needed from which to calculate a kinematicviscosity result that is the average of two acceptable deter-mined values.5. Significance and Use5.1 Many petroleum products, and some non-petroleummaterials, are used as lubricants, and the correct operation ofthe equipment depends upon the

27、appropriate viscosity of theliquid being used. In addition, the viscosity of many petroleumfuels is important for the estimation of optimum storage,handling, and operational conditions. Thus, the accurate deter-mination of viscosity is essential to many product specifica-tions.6. Apparatus6.1 Viscom

28、etersUse only calibrated viscometers of theglass capillary type, capable of being used to determinekinematic viscosity within the limits of the precision given inthe precision section.6.1.1 Viscometers listed in Table A1.1, whose specificationsmeet those given in Specifications D446 and in ISO 3105

29、meetthese requirements. It is not intended to restrict this test methodto the use of only those viscometers listed in TableA1.1.AnnexA1 gives further guidance.6.1.2 Automated ViscometersAutomated apparatus maybe used as long as they mimic the physical conditions,operations or processes of the manual

30、 apparatus. Any viscom-eter, temperature measuring device, temperature control, tem-perature controlled bath or timing device incorporated in theautomated apparatus shall conform to the specification forthese components as stated in Section 6 of this test method.Flow times of less than 200 s are per

31、mitted, however, a kineticenergy correction shall be applied in accordance with Section7 on Kinematic Viscosity Calculation of Specifications D446.The kinetic energy correction shall not exceed 3.0 % of themeasured viscosity. The automated apparatus shall be capableof determining kinematic viscosity

32、 of a certified viscosityreference standard within the limits stated in 9.2.1 and Section17. The precision shall be of statistical equivalence to, or better(has less variability) than the manual apparatus.NOTE 3Precision and bias of kinematic viscosity measurements forflow times of less than 200 s h

33、as not been determined. The precision statedin Section 17 is not know to be valid for kinematic viscosity measure-ments with flow times less than 200 s.3Available from American National Standards Institute (ANSI), 25 W. 43rd St.,4th Floor, New York, NY 10036.4Available from National Institute of Sta

34、ndards and Technology (NIST), 100Bureau Dr., Stop 3460, Gaithersburg, MD 20899-3460.D445 1026.2 Viscometer HoldersUse viscometer holders to enableall viscometers which have the upper meniscus directly abovethe lower meniscus to be suspended vertically within 1 in alldirections. Those viscometers who

35、se upper meniscus is offsetfrom directly above the lower meniscus shall be suspendedvertically within 0.3 in all directions (see Specifications D446and ISO 3105).6.2.1 Viscometers shall be mounted in the constant tempera-ture bath in the same manner as when calibrated and stated onthe certificate of

36、 calibration. See Specifications D446, seeOperating Instructions in Annexes A1A3. For those viscom-eters which have Tube L (see Specifications D446) heldvertical, vertical alignment shall be confirmed by using (1)aholder ensured to hold Tube L vertical, or (2) a bubble levelmounted on a rod designed

37、 to fit into Tube L, or (3) a plumbline suspended from the center of Tube L, or (4) other internalmeans of support provided in the constant temperature bath.6.3 Temperature-Controlled BathUse a transparent liquidbath of sufficient depth such, that at no time during themeasurement of flow time, any p

38、ortion of the sample in theviscometer is less than 20 mm below the surface of the bathliquid or less than 20 mm above the bottom of the bath.6.3.1 Temperature ControlFor each series of flow timemeasurements, the temperature control of the bath liquid shallbe such that within the range from 15 to 100

39、C, the tempera-ture of the bath medium does not vary by more than 60.02Cof the selected temperature over the length of the viscometer,or between the position of each viscometer, or at the location ofthe thermometer. For temperatures outside this range, thedeviation from the desired temperature must

40、not exceed60.05C.6.4 Temperature Measuring Device in the Range from 0 to100CUse either calibrated liquid-in-glass thermometers(Annex A2) of an accuracy after correction of 60.02C orbetter, or any other thermometric device of equal or betteraccuracy.6.4.1 If calibrated liquid-in-glass thermometers ar

41、e used, theuse of two thermometers is recommended. The two thermom-eters shall agree within 0.04C.6.4.2 Outside the range from 0 to 100C, use either cali-brated liquid-in-glass thermometers of an accuracy after cor-rection of 60.05C or better, or any other thermometric deviceof equal or better accur

42、acy. When two temperature measuringdevices are used in the same bath, they shall agree within60.1C.6.4.3 When using liquid-in-glass thermometers, such asthose in Table A2.1, use a magnifying device to read thethermometer to the nearest15 division (for example, 0.01C or0.02F) to ensure that the requi

43、red test temperature andtemperature control capabilities are met (see 10.1). It isrecommended that thermometer readings (and any correctionssupplied on the certificates of calibrations for the thermom-eters) be recorded on a periodic basis to demonstrate compli-ance with the test method requirements

44、. This information canbe quite useful, especially when investigating issues or causesrelating to testing accuracy and precision.6.5 Timing DeviceUse any timing device that is capableof taking readings with a discrimination of 0.1 s or better andhas an accuracy within 60.07 % (seeAnnexA3) of the read

45、ingwhen tested over the minimum and maximum intervals ofexpected flow times.6.5.1 Electrical timing devices may be used if the currentfrequency is controlled to an accuracy of 0.05 % or better.Alternating currents, as provided by some public power sys-tems, are intermittently rather than continuousl

46、y controlled.When used to actuate electrical timing devices, such controlcan cause large errors in kinematic viscosity flow time mea-surements.7. Reagents and Materials7.1 Chromic Acid Cleaning Solution, or a nonchromium-containing, strongly oxidizing acid cleaning solution.(WarningChromic acid is a

47、 health hazard. It is toxic, arecognized carcinogen, highly corrosive, and potentially haz-ardous in contact with organic materials. If used, wear a fullface-shield and full-length protective clothing including suit-able gloves. Avoid breathing vapor. Dispose of used chromicacid carefully as it rema

48、ins hazardous. Nonchromium-containing, strongly oxidizing acid cleaning solutions are alsohighly corrosive and potentially hazardous in contact withorganic materials, but do not contain chromium which hasspecial disposal problems.)7.2 Sample Solvent, completely miscible with the sample.Filter before

49、 use.7.2.1 For most samples a volatile petroleum spirit or naph-tha is suitable. For residual fuels, a prewash with an aromaticsolvent such as toluene or xylene may be necessary to removeasphaltenic material.7.3 Drying Solvent, a volatile solvent miscible with thesample solvent (see 7.2) and water (see 7.4). Filter before use.7.3.1 Acetone is suitable. (WarningExtremely flam-mable.)7.4 Water, deionized or distilled and conforming to Speci-fication D1193 or Grade 3 of ISO 3696. Filter before use.8. Certified Viscosity Reference Standards8.1 C