ASTM D7042-2012e1 5000 Standard Test Method for Dynamic Viscosity and Density of Liquids by Stabinger Viscometer (and the Calculation of Kinematic Viscosity)《用Stabinger粘度计 (和动粘度计算).pdf

《ASTM D7042-2012e1 5000 Standard Test Method for Dynamic Viscosity and Density of Liquids by Stabinger Viscometer (and the Calculation of Kinematic Viscosity)《用Stabinger粘度计 (和动粘度计算).pdf》由会员分享，可在线阅读，更多相关《ASTM D7042-2012e1 5000 Standard Test Method for Dynamic Viscosity and Density of Liquids by Stabinger Viscometer (and the Calculation of Kinematic Viscosity)《用Stabinger粘度计 (和动粘度计算).pdf（9页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D7042 121Standard Test Method forDynamic Viscosity and Density of Liquids by StabingerViscometer (and the Calculation of Kinematic Viscosity)1This standard is issued under the fixed designation D7042; the number immediately following the designation indicates the year oforiginal adoptio

2、n 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.1NOTEUpdated Table 2 editorially in August 2012.1. Scope*1.1 This test method covers an

3、d specifies a procedure for theconcurrent measurement of both the dynamic viscosity, h, andthe density, r, of liquid petroleum products and crude oils, bothtransparent and opaque. The kinematic viscosity, n, can beobtained by dividing the dynamic viscosity, h, by the density,r, obtained at the same

4、test temperature.1.2 The result 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 rate areproportional (Newtonian flow behavior).1.3 The precision has only been determined for thosemater

5、ials, viscosity ranges, density ranges, and temperatures asindicated in Section 15 on Precision and Bias. The test methodcan be applied to a wider range of materials, viscosity, density,and temperature. For materials not listed in Section 15 onPrecision and Bias, the precision and bias may not be ap

6、pli-cable.1.4 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to esta

7、blish appro-priate safety and health practices and to determine theapplicability of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D445 Test Method for Kinematic Viscosity of Transparentand Opaque Liquids (and Calculation of Dynamic Viscos-ity)D975 Specification for D

8、iesel Fuel OilsD2162 Practice for Basic Calibration of Master Viscometersand Viscosity Oil StandardsD2270 Practice for Calculating Viscosity Index from Kine-matic Viscosity at 40 and 100CD4052 Test Method for Density, Relative Density, and APIGravity of Liquids by Digital Density MeterD6299 Practice

9、 for Applying Statistical Quality Assuranceand Control Charting Techniques to Evaluate AnalyticalMeasurement System PerformanceD6300 Practice for Determination of Precision and BiasData for Use in Test Methods for Petroleum Products andLubricantsD6617 Practice for Laboratory Bias Detection Using Sin

10、gleTest Result from Standard MaterialD6708 Practice for Statistical Assessment and Improvementof Expected Agreement Between Two Test Methods thatPurport to Measure the Same Property of a Material2.2 ISO Standards:3ISO 5725 Accuracy (trueness and precision) of measurementmethods and resultsISO/IEC 17

11、025 General Requirements for the Competenceof Testing and Calibration Laboratories2.3 Other Documents:4NIST Technical Note 1297 Guideline for Evaluating andExpressing the Uncertainty of NIST Measurement Results3. Terminology3.1 Definitions:3.1.1 density (r), nmass per unit volume.3.1.2 dynamic visco

12、sity (h), nthe ratio between the ap-plied shear stress and rate of shear of a liquid.1This 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 April 15, 2012

13、. Published July 2012. Originallyapproved in 2004. Last previous edition approved in 2011 as D704211a.DOI:10.1520/D7042-12E01.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information,

14、 refer to the standards Document Summary page onthe ASTM website.3Available from American National Standards Institute (ANSI), 25 W. 43rd St.,4th Floor, New York, NY 10036, http:/www.ansi.org.4Available from National Institute of Standards and Technology (NIST), 100Bureau Dr., Stop 1070, Gaithersbur

15、g, MD 20899-1070, http:/www.nist.gov.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States13.1.2.1 DiscussionIt is sometimes called the coefficient ofdynamic viscosity or, sim

16、ply, viscosity. Thus, dynamic viscos-ity is a measure of the resistance to flow or to deformation ofa liquid under external shear forces.3.1.2.2 DiscussionThe term dynamic viscosity can also beused in a different context to denote a frequency-dependentquantity in which shear stress and shear rate ha

17、ve a sinusoidaltime dependence.3.1.3 kinematic viscosity (n), nthe ratio of the dynamicviscosity (h) to the density (r) of a liquid.3.1.3.1 DiscussionFor gravity flow under a given hydro-static head, the pressure head of a liquid is proportional to itsdensity (r). Therefore the kinematic viscosity (

18、n) is a measureof the resistance to flow of a liquid under gravity.3.1.4 relative density (also called specific gravity (SG),nthe ratio of the density of a material at a stated temperatureto the density of a reference material (usually water) at a statedtemperature.4. Summary of Test Method4.1 The t

19、est specimen is introduced into the measuring cells,which are at a closely controlled and known temperature. Themeasuring cells consist of a pair of rotating concentric cylin-ders and an oscillating U-tube. The dynamic viscosity isdetermined from the equilibrium rotational speed of the innercylinder

20、 under the influence of the shear stress of the testspecimen and an eddy current brake in conjunction withadjustment data. The density is determined by the oscillationfrequency of the U-tube in conjunction with adjustment data.The kinematic viscosity is calculated by dividing the dynamicviscosity by

21、 the density.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 appropriate viscosity of theliquid being used. In addition, the viscosity of many petroleumfuels is important for the es

22、timation of optimum storage,handling, and operational conditions. Thus, the accurate deter-mination of viscosity is essential to many product specifica-tions.5.2 Density is a fundamental physical property that can beused in conjunction with other properties to characterize boththe light and heavy fr

23、actions of petroleum and petroleumproducts.5.3 Determination of the density or relative density ofpetroleum and its products is necessary for the conversion ofmeasured volumes to volumes at the standard temperature of15C.6. Apparatus6.1 Stabinger Viscometer5,66.1.1 Viscosity MeasurementThe Stabinger

24、 viscometeruses a rotational coaxial cylinder measuring system. The outercylinder (tube) is driven by a motor at a constant and knownrotational speed. The low-density inner cylinder (rotor) is heldin the axis of rotation by the centrifugal forces of the higherdensity sample and in its longitudinal p

25、osition by the magnetand the soft iron ring. Consequently, the system works free ofbearing friction as found in rotational viscometers. A perma-nent magnet in the inner cylinder induces eddy currents in thesurrounding copper casing. The rotational speed of the innercylinder establishes itself as the

26、 result of the equilibriumbetween the driving torque of the viscous forces and theretarding eddy current torque. This rotational speed is mea-sured by an electronic system (Hall effect sensor) by countingthe frequency of the rotating magnetic field (see Fig. 1 and Fig.2, No. 2).6.1.2 Density Measure

27、mentThe digital density analyzeruses a U-shaped oscillating sample tube and a system forelectronic excitation and frequency counting (see Fig. 2, No.3).6.1.3 Temperature ControlThe copper block surroundsboth the viscosity and the density measuring cell in a way thatboth cells are held at the same te

28、mperature. A thermoelectricheating and cooling system (see Fig. 2, No. 1) ensures thetemperature stability of the copper block within 60.005Cfrom the set temperature at the position of the viscosity cellover the whole temperature range. The uncertainty (k = 2; 95 %confidence level) of the temperatur

29、e calibration shall be nomore than 60.03C over the range from 15 to 100C. Outsidethis range the calibration uncertainty shall be no more than60.05C.6.1.4 The thermal equilibration time depends on the heatcapacity and conductivity of the liquid and on the differencebetween injection temperature and t

30、est temperature. Adequatetemperature equilibration of the test specimen is automaticallydetermined when successive viscosity values are constantwithin 60.07 % over 1 min and successive density values areconstant within 60.00003 g/cm3over 60 s.5The Stabinger viscometer is covered by a patent. Interes

31、ted parties are invitedto submit information regarding the identification of an alternative to this patenteditem to the ASTM International headquarters. Your comments will receive carefulconsideration at a meeting of the responsible technical committee, which you mayattend.6The sole source of supply

32、 of the apparatus known to the committee at this timeis Anton Paar GmbH, Anton-Paar-Str. 20, A-8054 Graz, Austria. If you are aware ofalternative suppliers, please provide this information to ASTM Internationalheadquarters. Your comments will receive careful consideration at a meeting of theresponsi

33、ble technical committee, which you may attend.FIG. 1 Viscosity CellD7042 1212NOTE 1The Stabinger Viscometer, manufactured by Anton PaarGmbH, fulfills the stated requirements when operated in the most precisemode of operation.6.2 Syringes, commercially available, at least 5 mL involume, with a Luer t

34、ip.All construction materials for syringesshall be fully compatible with all sample liquids and cleaningagents, which contact them.6.3 Flow-Through or Pressure Adapter, for use as an alter-native means of introducing the test specimen into the mea-suring cells either by pressure or by suction, provi

35、ded thatsufficient care and control is used to avoid any bubbleformation in the test specimen. All construction materials foradaptors shall be fully compatible with all sample liquids andcleaning agents, which contact them.6.4 Autosampler, for use in automated injection analyses.The autosampler shal

36、l be designed to ensure the integrity of thetest specimen prior to and during the analysis and be equippedto transfer a representative portion of test specimen into themeasuring cells. The autosampler shall transfer the test speci-men from the sample vial to the measuring cells of theapparatus witho

37、ut interfering with the integrity of the testspecimen. The autosampler shall be able to mimic the proce-dure for sample handling as set forth in 11.1 and 11.2. Theautosampler may have heating capability as a means to lowerthe viscosity of the sample for filling the measuring cells.6.5 Screen, with a

38、n aperture of 75 m, to remove particlesfrom the sample.6.6 Magnet, strong enough to remove iron fillings from thesample. Magnetic stirring rods are suitable.7. Reagents and Materials7.1 Sample Solvent, completely miscible with the sample.7.1.1 For most samples, a volatile petroleum spirit ornaphtha

39、is suitable. If the solvent dries up without residues inan applicable time frame, the use of a separate drying solventis not required.7.1.2 For residual fuels, a prewash with an aromatic solventsuch as toluene or xylene may be necessary to remove asphalticmaterial.7.2 Drying Solvent, a volatile solv

40、ent miscible with thesample solvent (see 7.1).7.2.1 Highly concentrated ethanol (96 % or higher) is suit-able.7.3 Dry Air or Nitrogen, for blowing the measuring cells.7.3.1 If the measuring cell temperature is below or near thedew point temperature of the ambient air, the use of anappropriate desicc

41、ator is required.8. Sampling, Test Specimens, and Test Units8.1 Sampling is defined as all the steps required to obtain analiquot of the contents of any pipe, tank, or other system, andto place the sample into the laboratory test container. Thelaboratory test container and sample volume shall be ofs

42、ufficient capacity to mix the sample and obtain a homoge-neous sample for analysis.8.2 ParticlesFor samples that are likely to contain par-ticles (for example, used oils or crude oils) pass the samplethrough a 75-m screen to remove the particles. For theremoval of iron filings the use of a magnet is

43、 appropriate. Waxysamples must be heated to dissolve the wax crystals prior tofiltration and a preheated filter shall be used.8.3 Test SpecimenAportion or volume of sample obtainedfrom the laboratory sample and delivered to the measuringcells. The test specimen is obtained as follows:8.3.1 Mix the s

44、ample, if required, to homogenize. Mixing atroom temperature in an open container can result in the loss ofvolatile material; mixing in closed, pressurized containers, or atsub-ambient temperatures is recommended.8.3.2 Draw the test specimen from a properly mixed labo-ratory sample using an appropri

45、ate syringe.Alternatively, if theproper attachments and connecting tubes are used, the testspecimen may be delivered directly to the measuring cellsusing a flow through or pressure adapter (see 6.3) or autosam-pler (see 6.4) from the mixing container. For waxy or othersamples with a high pour point,

46、 before drawing the testspecimen, heat the laboratory sample to the desired testtemperature, which has to be high enough to dissolve the waxcrystals.9. Calibration and Verification9.1 Use only a calibrated apparatus as described in 6.1. Thecalibration shall be checked periodically using certified re

47、fer-ence standards as described in 9.2 and 9.3. The recommendedinterval for viscosity and density calibration is once a month,for temperature control once a year. For the calibrationprocedure follow the instructions of the manufacturer of theapparatus.9.2 Certified Viscosity and Density Reference St

48、andardsThese are for use as confirmatory checks on the procedure inthe laboratory. Certified viscosity and density reference stan-dards shall be certified by a laboratory, which has shown tomeet the requirements of ISO/IEC 17025 or a correspondingnational standard by independent assessment. Viscosit

49、y stan-dards shall be traceable to master viscometer proceduresdescribed in Test Method D2162. Density standards shall havea certified uncertainty of the density values of 0.0001 g/cm3.FIG. 2 Cell BlockD7042 1213The uncertainty of the reference standards shall be stated foreach certified value (k = 2; 95 % confidence level). See ISO5725 or NIST Technical Note 1297.9.3 ThermometerFor calibration and adjustment of thetemperature control, a digital thermometer with a probe diam-eter of 6.25 mm and a maximal length of 80 mm shall be used.For smaller probe