ASTM D 257-2007 DC Resistance or Conductance of Insulating Materials

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ASTMD 中文 绝缘材料直流电阻和电导测试…

ASTMD 中文 绝缘材料直流电阻和电导测试…

ASTMD257-07中文版绝缘材料直流电阻和电导测试.…ASTMD绝缘材料直流电阻或电导的标准试验方法本标准是以固定代号D发布的。

其后的数字表示原文本正式通过的年号在有修订的情况下为上一次的修订年号圆括号中数字为上一次重新确认的年号。

上标符号(ε)表示对上次修改或重新确定的版本有编辑上的修改。

本标准经批准用于国防部所有机构。

1.范围本试验方法包含直流绝缘电阻体积电阻和表面电阻的测量所用直流程序。

通过该测量及样本和电极的几何尺寸可以计算出电绝缘材料的体积电阻和表面电阻同时还可以计算出相应的电导和电导率。

这些试验方法不适用于测量中等导电材料的电阻电导。

这些材料评估可采用试验方法D4496。

本标准描述了几种可选择的测量电阻(或电导)的普通方法。

特殊材料科采用最合适的标准ASTM试验方法进行测试这些特殊材料具有电压应力范围和有限起电时间同时规定了样本结构和电极几何形状。

这些个别特殊试验方法将能更好得定义测量值的精度和偏差。

本试验方法包括以下章节:试验方法或步骤章节计算13设备和试验方法的选择7清洗固体样本10.1样本的状态调节11屏蔽电极的有效面积附录X2电极系6绝缘电阻或电导材料的影响因素附录X1湿度控制11.2液体样本和电池9.4精度和偏差15电阻或电导测量步骤12引用文件2报告14抽样8重要性和用途5样本安装10试验方法摘要4术语3绝缘电阻体积电阻和表面电阻或电导测量用试验样本9典型测量方法附录X3本标准并没有完全列举所有的安全声明如果有必要根据实际使用情况进行斟酌。

使用本规范前使用者有责任制定符合安全和健康要求的条例和规范并明确该规范的使用范围。

引用文件ASTM标准:D150固体电绝缘材料的(恒久电介质)的交流损耗特性和介电常数的测试方法D374固体电绝缘材料厚度的标准试验方法D1169电绝缘液电阻率(电阻系数)试验方法D1711电绝缘相关术语D4496中等导电材料直流电阻或导电性的标准试验方法D5032用水甘油溶液设备维持恒定相关湿度的规程D6054测试用电工绝缘材料的调节规程E104用水溶液保持相对恒定湿度的标准实施规程术语定义:以下定义直接来自术语标准D1711适用于本标准正文所用术语。

ASTM D 790-2007(弯曲)

ASTM D 790-2007(弯曲)

Designation:D790–07Standard Test Methods forFlexural Properties of Unreinforced and Reinforced Plastics and Electrical Insulating Materials1This standard is issued under thefixed designation D790;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A superscript epsilon(e)indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1.Scope*1.1These test methods cover the determination offlexural properties of unreinforced and reinforced plastics,including high-modulus composites and electrical insulating materials in the form of rectangular bars molded directly or cut from sheets, plates,or molded shapes.These test methods are generally applicable to both rigid and semirigid materials.However,flexural strength cannot be determined for those materials that do not break or that do not fail in the outer surface of the test specimen within the5.0%strain limit of these test methods. These test methods utilize a three-point loading system applied to a simply supported beam.A four-point loading system method can be found in Test Method D6272.1.1.1Procedure A,designed principally for materials that break at comparatively small deflections.1.1.2Procedure B,designed particularly for those materials that undergo large deflections during testing.1.1.3Procedure A shall be used for measurement offlexural properties,particularlyflexural modulus,unless the material specification states otherwise.Procedure B may be used for measurement offlexural strength only.Tangent modulus data obtained by Procedure A tends to exhibit lower standard deviations than comparable data obtained by means of Proce-dure B.1.2Comparative tests may be run in accordance with either procedure,provided that the procedure is found satisfactory for the material being tested.1.3The values stated in SI units are to be regarded as the standard.The values provided in brackets are for information only.1.4This standard does not purport to address all of the safety concerns,if any,associated with its use.It is the responsibility 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.N OTE1—These test methods are not technically equivalent to ISO178.2.Referenced Documents2.1ASTM Standards:2D618Practice for Conditioning Plastics for TestingD638Test Method for Tensile Properties of PlasticsD883Terminology Relating to PlasticsD4000Classification System for Specifying Plastic Mate-rialsD4101Specification for Polypropylene Injection and Ex-trusion MaterialsD5947Test Methods for Physical Dimensions of Solid Plastics SpecimensD6272Test Method for Flexural Properties of Unrein-forced and Reinforced Plastics and Electrical Insulating Materials by Four-Point BendingE4Practices for Force Verification of Testing Machines E691Practice for Conducting an Interlaboratory Study to Determine the Precision of a Test Method2.2ISO Standard:3ISO178Plastics—Determination of Flexural Properties of Rigid Plastics3.Terminology3.1Definitions—Definitions of terms applying to these test methods appear in Terminology D883and Annex A1of Test Method D638.4.Summary of Test Method4.1A bar of rectangular cross section rests on two supports and is loaded by means of a loading nose midway between the supports.A support span-to-depth ratio of16:1shall be used unless there is reason to suspect that a larger span-to-depth ratio may be required,as may be the case for certain laminated materials(see Section7and Note7for guidance).1These test methods are under the jurisdiction of ASTM Committee D20on Plastics and are the direct responsibility of Subcommittee D20.10on Mechanical Properties.Current edition approved Sept.1,2007.Published October2007.Originally approved st previous edition approved in2003as D790–03.2For referenced ASTM standards,visit the ASTM website,,or contact ASTM Customer Service at service@.For Annual Book of ASTM Standards volume information,refer to the standard’s Document Summary page on the ASTM website.3Available from American National Standards Institute(ANSI),25W.43rd St., 4th Floor,New York,NY10036,.*A Summary of Changes section appears at the end of this standard. Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States.4.2The specimen is deflected until rupture occurs in the outer surface of the test specimen or until a maximum strain (see 12.7)of5.0%is reached,whichever occurs first.4.3Procedure A employs a strain rate of 0.01mm/mm/min [0.01in./in./min]and is the preferred procedure for this test method,while Procedure B employs a strain rate of 0.10mm/mm/min [0.10in./in./min].5.Significance and Use5.1Flexural properties as determined by these test methods are especially useful for quality control and specification purposes.5.2Materials that do not fail by the maximum strain allowed under these test methods (3-point bend)may be more suited to a 4-point bend test.The basic difference between the two test methods is in the location of the maximum bending moment and maximum axial fiber stresses.The maximum axial fiber stresses occur on a line under the loading nose in 3-point bending and over the area between the loading noses in 4-point bending.5.3Flexural properties may vary with specimen depth,temperature,atmospheric conditions,and the difference in rate of straining as specified in Procedures A and B (see also Note 7).5.4Before proceeding with these test methods,reference should be made to the ASTM specification of the material being tested.Any test specimen preparation,conditioning,dimensions,or testing parameters,or combination thereof,covered in the ASTM material specification shall take prece-dence over those mentioned in these test methods.Table 1in Classification System D 4000lists the ASTM material speci-fications that currently exist for plastics.6.Apparatus6.1Testing Machine —A properly calibrated testing ma-chine that can be operated at constant rates of crosshead motion over the range indicated,and in which the error in the load measuring system shall not exceed 61%of the maximum load expected to be measured.It shall be equipped with a deflection measuring device.The stiffness of the testing machine shall be such that the total elastic deformation of the system does not exceed 1%of the total deflection of the test specimen duringtesting,or appropriate corrections shall be made.The load indicating mechanism shall be essentially free from inertial lag at the crosshead rate used.The accuracy of the testing machine shall be verified in accordance with Practices E 4.6.2Loading Noses and Supports —The loading nose and supports shall have cylindrical surfaces.The default radii of the loading nose and supports shall be 5.060.1mm [0.19760.004in.]unless otherwise specified in an ASTM material specification or as agreed upon between the interested parties.When the use of an ASTM material specification,or an agreed upon modification,results in a change to the radii of the loading nose and supports,the results shall be clearly identified as being obtained from a modified version of this test method and shall include the specification (when available)from which the modification was specified,for example,Test Method D 790in accordance with Specification D 4101.6.2.1Other Radii for Loading Noses and Supports —When other than default loading noses and supports are used,in order to avoid excessive indentation,or failure due to stress concen-tration directly under the loading nose,they must comply with the following requirements:they shall have a minimum radius of 3.2mm [1⁄8in.]for all specimens.For specimens 3.2mm or greater in depth,the radius of the supports may be up to 1.6times the specimen depth.They shall be this large if significant indentation or compressive failure occurs.The arc of the loading nose in contact with the specimen shall be sufficiently large to prevent contact of the specimen with the sides of the nose.The maximum radius of the loading nose shall be no more than four times the specimen depth.6.3Micrometers —Suitable micrometers for measuring the width and thickness of the test specimen to an incremental discrimination of at least 0.025mm [0.001in.]should be used.All width and thickness measurements of rigid and semirigid plastics may be measured with a hand micrometer with ratchet.A suitable instrument for measuring the thickness of nonrigid test specimens shall have:a contact measuring pressure of 2562.5kPa [3.660.36psi],a movable circular contact foot 6.3560.025mm [0.25060.001in.]in diameter and a lower fixed anvil large enough to extend beyond the contact foot in all directions and being parallel to the contact foot within 0.005mm [0.002in.]over the entire foot area.Flatness of foot and anvil shall conform to the portion of the Calibration section of Test Methods D 5947.7.Test Specimens7.1The specimens may be cut from sheets,plates,or molded shapes,or may be molded to the desired finished dimensions.The actual dimensions used in Section 4.2,Cal-culation,shall be measured in accordance with Test Methods D 5947.N OTE 2—Any necessary polishing of specimens shall be done only in the lengthwise direction of the specimen.7.2Sheet Materials (Except Laminated Thermosetting Ma-terials and Certain Materials Used for Electrical Insulation,Including Vulcanized Fiber and Glass Bonded Mica):7.2.1Materials 1.6mm [1⁄16in.]or Greater in Thickness —For flatwise tests,the depth of the specimen shall be the thickness of the material.For edgewise tests,the width of theTABLE 1Flexural StrengthMaterial Mean,103psiValues Expressed in Units of %of 103psi V r A V R B r C R D ABS9.99 1.59 6.05 4.4417.2DAP thermoset 14.3 6.58 6.5818.618.6Cast acrylic 16.3 1.6711.3 4.7332.0GR polyester19.5 1.43 2.14 4.05 6.08GR polycarbonate 21.0 5.16 6.0514.617.1SMC26.04.767.1913.520.4AV r =within-laboratory coefficient of variation for the indicated material.It is obtained by first pooling the within-laboratory standard deviations of the test results from all of the participating laboratories:Sr =[[(s 1)2+(s 2)2...+(s n )2]/n]1/2then V r =(S r divided by the overall average for the material)3100.BV r =between-laboratory reproducibility,expressed as the coefficient of varia-tion:S R ={S r 2+S L 2}1/2where S L is the standard deviation of laboratory means.Then:V R =(S R divided by the overall average for the material)3100.Cr =within-laboratory critical interval between two test results =2.83V r .DR =between-laboratory critical interval between two test results =2.83V R.specimen shall be the thickness of the sheet,and the depth shall not exceed the width(see Notes3and4).For all tests,the support span shall be16(tolerance61)times the depth of the beam.Specimen width shall not exceed one fourth of the support span for specimens greater than3.2mm[1⁄8in.]in depth.Specimens3.2mm or less in depth shall be12.7mm[1⁄2 in.]in width.The specimen shall be long enough to allow for overhanging on each end of at least10%of the support span, but in no case less than6.4mm[1⁄4in.]on each end.Overhang shall be sufficient to prevent the specimen from slipping through the supports.N OTE3—Whenever possible,the original surface of the sheet shall be unaltered.However,where testing machine limitations make it impossible to follow the above criterion on the unaltered sheet,one or both surfaces shall be machined to provide the desired dimensions,and the location of the specimens with reference to the total depth shall be noted.The value obtained on specimens with machined surfaces may differ from those obtained on specimens with original surfaces.Consequently,any specifi-cations forflexural properties on thicker sheets must state whether the original surfaces are to be retained or not.When only one surface was machined,it must be stated whether the machined surface was on the tension or compression side of the beam.N OTE4—Edgewise tests are not applicable for sheets that are so thin that specimens meeting these requirements cannot be cut.If specimen depth exceeds the width,buckling may occur.7.2.2Materials Less than1.6mm[1⁄16in.]in Thickness—The specimen shall be50.8mm[2in.]long by12.7mm[1⁄2in.] wide,testedflatwise on a25.4-mm[1-in.]support span.N OTE5—Use of the formulas for simple beams cited in these test methods for calculating results presumes that beam width is small in comparison with the support span.Therefore,the formulas do not apply rigorously to these dimensions.N OTE6—Where machine sensitivity is such that specimens of these dimensions cannot be measured,wider specimens or shorter support spans,or both,may be used,provided the support span-to-depth ratio is at least14to1.All dimensions must be stated in the report(see also Note5).7.3Laminated Thermosetting Materials and Sheet and Plate Materials Used for Electrical Insulation,Including Vulcanized Fiber and Glass-Bonded Mica—For paper-base and fabric-base grades over25.4mm[1in.]in nominal thickness,the specimens shall be machined on both surfaces to a depth of25.4mm.For glass-base and nylon-base grades, specimens over12.7mm[1⁄2in.]in nominal depth shall be machined on both surfaces to a depth of12.7mm.The support span-to-depth ratio shall be chosen such that failures occur in the outerfibers of the specimens,due only to the bending moment(see Note7).Therefore,a ratio larger than16:1may be necessary(32:1or40:1are recommended).When laminated materials exhibit low compressive strength perpendicular to the laminations,they shall be loaded with a large radius loading nose(up to four times the specimen depth to prevent premature damage to the outerfibers.7.4Molding Materials(Thermoplastics and Thermosets)—The recommended specimen for molding materials is127by 12.7by3.2mm[5by1⁄2by1⁄8in.]testedflatwise on a support span,resulting in a support span-to-depth ratio of16(tolerance 61).Thicker specimens should be avoided if they exhibit significant shrink marks or bubbles when molded.7.5High-Strength Reinforced Composites,Including Highly Orthotropic Laminates—The span-to-depth ratio shall be cho-sen such that failure occurs in the outerfibers of the specimens and is due only to the bending moment(see Note7).A span-to-depth ratio larger than16:1may be necessary(32:1or 40:1are recommended).For some highly anisotropic compos-ites,shear deformation can significantly influence modulus measurements,even at span-to-depth ratios as high as40:1. Hence,for these materials,an increase in the span-to-depth ratio to60:1is recommended to eliminate shear effects when modulus data are required,it should also be noted that the flexural modulus of highly anisotropic laminates is a strong function of ply-stacking sequence and will not necessarily correlate with tensile modulus,which is not stacking-sequence dependent.N OTE7—As a general rule,support span-to-depth ratios of16:1are satisfactory when the ratio of the tensile strength to shear strength is less than8to1,but the support span-to-depth ratio must be increased for composite laminates having relatively low shear strength in the plane of the laminate and relatively high tensile strength parallel to the support span.8.Number of Test Specimens8.1Test at leastfive specimens for each sample in the case of isotropic materials or molded specimens.8.2For each sample of anisotropic material in sheet form, test at leastfive specimens for each of the following conditions. Recommended conditions areflatwise and edgewise tests on specimens cut in lengthwise and crosswise directions of the sheet.For the purposes of this test,“lengthwise”designates the principal axis of anisotropy and shall be interpreted to mean the direction of the sheet known to be stronger inflexure.“Cross-wise”indicates the sheet direction known to be the weaker in flexure and shall be at90°to the lengthwise direction.9.Conditioning9.1Conditioning—Condition the test specimens at236 2°C[73.463.6°F]and5065%relative humidity for not less than40h prior to test in accordance with Procedure A of Practice D618unless otherwise specified by contract or the relevant ASTM material specification.Reference pre-test con-ditioning,to settle disagreements,shall apply tolerances of 61°C[1.8°F]and62%relative humidity.9.2Test Conditions—Conduct the tests at2362°C[73.46 3.6°F]and5065%relative humidity unless otherwise specified by contract or the relevant ASTM material specifica-tion.Reference testing conditions,to settle disagreements, shall apply tolerances of61°C[1.8°F]and62%relative humidity.10.Procedure10.1Procedure A:10.1.1Use an untested specimen for each measurement. Measure the width and depth of the specimen to the nearest 0.03mm[0.001in.]at the center of the support span.For specimens less than2.54mm[0.100in.]in depth,measure the depth to the nearest0.003mm[0.0005in.].These measure-ments shall be made in accordance with Test Methods D5947.10.1.2Determine the support span to be used as described in Section7and set the support span to within1%of the determinedvalue.10.1.3Forflexuralfixtures that have continuously adjust-able spans,measure the span accurately to the nearest0.1mm [0.004in.]for spans less than63mm[2.5in.]and to the nearest 0.3mm[0.012in.]for spans greater than or equal to63mm [2.5in.].Use the actual measured span for all calculations.For flexuralfixtures that havefixed machined span positions,verify the span distance the same as for adjustable spans at each machined position.This distance becomes the span for that position and is used for calculations applicable to all subse-quent tests conducted at that position.See Annex A2for information on the determination of and setting of the span.10.1.4Calculate the rate of crosshead motion as follows and set the machine for the rate of crosshead motion as calculated by Eq1:R5ZL2/6d(1) where:R=rate of crosshead motion,mm[in.]/min,L=support span,mm[in.],d=depth of beam,mm[in.],andZ=rate of straining of the outerfiber,mm/mm/min[in./ in./min].Z shall be equal to0.01.In no case shall the actual crosshead rate differ from that calculated using Eq1,by more than610%.10.1.5Align the loading nose and supports so that the axes of the cylindrical surfaces are parallel and the loading nose is midway between the supports.The parallelism of the apparatus may be checked by means of a plate with parallel grooves into which the loading nose and supports willfit when properly aligned(see A2.3).Center the specimen on the supports,with the long axis of the specimen perpendicular to the loading nose and supports.10.1.6Apply the load to the specimen at the specified crosshead rate,and take simultaneous load-deflection data. Measure deflection either by a gage under the specimen in contact with it at the center of the support span,the gage being mounted stationary relative to the specimen supports,or by measurement of the motion of the loading nose relative to the supports.Load-deflection curves may be plotted to determine theflexural strength,chord or secant modulus or the tangent modulus of elasticity,and the total work as measured by the area under the load-deflection curve.Perform the necessary toe compensation(see Annex A1)to correct for seating and indentation of the specimen and deflections in the machine.10.1.7Terminate the test when the maximum strain in the outer surface of the test specimen has reached0.05mm/mm [in./in.]or at break if break occurs prior to reaching the maximum strain(Notes8and9).The deflection at which this strain will occur may be calculated by letting r equal0.05 mm/mm[in./in.]in Eq2:D5rL2/6d(2) where:D=midspan deflection,mm[in.],r=strain,mm/mm[in./in.],L=support span,mm[in.],andd=depth of beam,mm[in.].N OTE8—For some materials that do not yield or break within the5% strain limit when tested by Procedure A,the increased strain rate allowed by Procedure B(see10.2)may induce the specimen to yield or break,or both,within the required5%strain limit.N OTE9—Beyond5%strain,this test method is not applicable.Some other mechanical property might be more relevant to characterize mate-rials that neither yield nor break by either Procedure A or Procedure B within the5%strain limit(for example,Test Method D638may be considered).10.2Procedure B:10.2.1Use an untested specimen for each measurement.10.2.2Test conditions shall be identical to those described in10.1,except that the rate of straining of the outer surface of the test specimen shall be0.10mm/mm[in./in.]/min.10.2.3If no break has occurred in the specimen by the time the maximum strain in the outer surface of the test specimen has reached0.05mm/mm[in./in.],discontinue the test(see Note9).11.Retests11.1Values for properties at rupture shall not be calculated for any specimen that breaks at some obvious,fortuitousflaw, unless suchflaws constitute a variable being studied.Retests shall be made for any specimen on which values are not calculated.12.Calculation12.1Toe compensation shall be made in accordance with Annex A1unless it can be shown that the toe region of the curve is not due to the take-up of slack,seating of the specimen,or other artifact,but rather is an authentic material response.12.2Flexural Stress(s f)—When a homogeneous elastic material is tested inflexure as a simple beam supported at two points and loaded at the midpoint,the maximum stress in the outer surface of the test specimen occurs at the midpoint.This stress may be calculated for any point on the load-deflection curve by means of the following equation(see Notes10-12):s f53PL/2bd2(3) where:s=stress in the outerfibers at midpoint,MPa[psi],P=load at a given point on the load-deflection curve,N [lbf],L=support span,mm[in.],b=width of beam tested,mm[in.],andd=depth of beam tested,mm[in.].N OTE10—Eq3applies strictly to materials for which stress is linearly proportional to strain up to the point of rupture and for which the strains are small.Since this is not always the case,a slight error will be introduced if Eq3is used to calculate stress for materials that are not true Hookean materials.The equation is valid for obtaining comparison data and for specification purposes,but only up to a maximumfiber strainof5%in the outer surface of the test specimen for specimens tested by the procedures described herein.N OTE11—When testing highly orthotropic laminates,the maximum stress may not always occur in the outer surface of the test specimen.4 Laminated beam theory must be applied to determine the maximum tensile stress at failure.If Eq3is used to calculate stress,it will yield an apparent strength based on homogeneous beam theory.This apparent strength is highly dependent on the ply-stacking sequence of highly orthotropic laminates.N OTE12—The preceding calculation is not valid if the specimen slips excessively between the supports.12.3Flexural Stress for Beams Tested at Large Support Spans(s f)—If support span-to-depth ratios greater than16to 1are used such that deflections in excess of10%of the support span occur,the stress in the outer surface of the specimen for a simple beam can be reasonably approximated with the following equation(see Note13):s f5~3PL/2bd2!@116~D/L!224~d/L!~D/L!#(4) where:s f,P,L,b,and d are the same as for Eq3,andD=deflection of the centerline of the specimen at the middle of the support span,mm[in.].N OTE13—When large support span-to-depth ratios are used,significant end forces are developed at the support noses which will affect the moment in a simple supported beam.Eq4includes additional terms that are an approximate correction factor for the influence of these end forces in large support span-to-depth ratio beams where relatively large deflec-tions exist.12.4Flexural Strength(s fM)—Maximumflexural stress sustained by the test specimen(see Note11)during a bendingtest.It is calculated according to Eq3or Eq4.Some materials that do not break at strains of up to5%may give a load deflection curve that shows a point at which the load does not increase with an increase in strain,that is,a yield point(Fig.1, Curve B),Y.Theflexural strength may be calculated for these materials by letting P(in Eq3or Eq4)equal this point,Y.12.5Flexural Offset Yield Strength—Offset yield strength is the stress at which the stress-strain curve deviates by a given strain(offset)from the tangent to the initial straight line portion of the stress-strain curve.The value of the offset must be given whenever this property is calculated.N OTE14—This value may differ fromflexural strength defined in12.4. Both methods of calculation are described in the annex to Test Method D638.12.6Flexural Stress at Break(s fB)—Flexural stress at break of the test specimen during a bending test.It is calculated according to Eq3or Eq4.Some materials may give a load deflection curve that shows a break point,B,without a yield point(Fig.1,Curve a)in which case s fB=s fM.Other materials may give a yield deflection curve with both a yield and a break point,B(Fig.1,Curve b).Theflexural stress at break may be calculated for these materials by letting P(in Eq 3or Eq4)equal this point,B.12.7Stress at a Given Strain—The stress in the outer surface of a test specimen at a given strain may be calculated in accordance with Eq3or Eq4by letting P equal the load read from the load-deflection curve at the deflection corresponding to the desired strain(for highly orthotropic laminates,see Note11).12.8Flexural Strain,e f—Nominal fractional change in the length of an element of the outer surface of the test specimen at midspan,where the maximum strain occurs.It may be calculated for any deflection using Eq5:e f56Dd/L2(5) where:e f=strain in the outer surface,mm/mm[in./in.],D=maximum deflection of the center of the beam,mm [in.],L=support span,mm[in.],andd=depth,mm[in.].12.9Modulus of Elasticity:12.9.1Tangent Modulus of Elasticity—The tangent modu-lus of elasticity,often called the“modulus of elasticity,”is the ratio,within the elastic limit,of stress to corresponding strain. It is calculated by drawing a tangent to the steepest initial straight-line portion of the load-deflection curve and using Eq 6(for highly anisotropic composites,see Note15).E B5L3m/4bd3(6)4For a discussion of these effects,see Zweben,C.,Smith,W.S.,and Wardle,M. W.,“Test Methods for Fiber Tensile Strength,Composite Flexural Modulus and Properties of Fabric-Reinforced Laminates,“Composite Materials:Testing and Design(Fifth Conference),ASTM STP674,1979,pp.228–262.N OTE—Curve a:Specimen that breaks before yielding.Curve b:Specimen that yields and then breaks before the5%strain limit.Curve c:Specimen that neither yields nor breaks before the5%strain limit.FIG.1Typical Curves of Flexural Stress(ßf)Versus FlexuralStrain(ef)where:E B =modulus of elasticity in bending,MPa [psi],L =support span,mm [in.],b =width of beam tested,mm [in.],d =depth of beam tested,mm [in.],andm =slope of the tangent to the initial straight-line portion of the load-deflection curve,N/mm [lbf/in.]of deflec-tion.N OTE 15—Shear deflections can seriously reduce the apparent modulusof highly anisotropic composites when they are tested at low span-to-depth ratios.4For this reason,a span-to-depth ratio of 60to 1is recommended for flexural modulus determinations on these composites.Flexural strength should be determined on a separate set of replicate specimens at a lower span-to-depth ratio that induces tensile failure in the outer fibers of the beam along its lower face.Since the flexural modulus of highly anisotropic laminates is a critical function of ply-stacking sequence,it will not necessarily correlate with tensile modulus,which is not stacking-sequence dependent.12.9.2Secant Modulus —The secant modulus is the ratio of stress to corresponding strain at any selected point on the stress-strain curve,that is,the slope of the straight line that joins the origin and a selected point on the actual stress-strain curve.It shall be expressed in megapascals [pounds per square inch].The selected point is chosen at a prespecified stress or strain in accordance with the appropriate material specification or by customer contract.It is calculated in accordance with Eq 6by letting m equal the slope of the secant to the load-deflection curve.The chosen stress or strain point used for the determination of the secant shall be reported.12.9.3Chord Modulus (E f )—The chord modulus may be calculated from two discrete points on the load deflection curve.The selected points are to be chosen at two prespecified stress or strain points in accordance with the appropriate material specification or by customer contract.The chosen stress or strain points used for the determination of the chord modulus shall be reported.Calculate the chord modulus,E f using the following equation:E f 5~s f 22s f 1!/~e f 22e f 1!(7)where:s f 2and s f 1are the flexural stresses,calculated from Eq 3or Eq 4and measured at the predefined points on the loaddeflection curve,and e f 2ande f 1are the flexural strain values,calculated from Eq 5and measured at the predetermined points on the load deflection curve.12.10Arithmetic Mean —For each series of tests,the arithmetic mean of all values obtained shall be calculated to three significant figures and reported as the “average value”for the particular property in question.12.11Standard Deviation —The standard deviation (esti-mated)shall be calculated as follows and be reported to two significant figures:s 5=~(X 22nX¯2!/~n 21!(8)where:s =estimated standard deviation,X =value of single observation,n =number of observations,andX ¯=arithmetic mean of the set of observations.13.Report13.1Report the following information:13.1.1Complete identification of the material tested,includ-ing type,source,manufacturer’s code number,form,principal dimensions,and previous history (for laminated materials,ply-stacking sequence shall be reported),13.1.2Direction of cutting and loading specimens,when appropriate,13.1.3Conditioning procedure,13.1.4Depth and width of specimen,13.1.5Procedure used (A or B),13.1.6Support span length,13.1.7Support span-to-depth ratio if different than 16:1,13.1.8Radius of supports and loading noses,if different than 5mm.When support and/or loading nose radii other than 5mm are used,the results shall be identified as being generated by a modified version of this test method and the referring specification referenced as to the geometry used.13.1.9Rate of crosshead motion,13.1.10Flexural strain at any given stress,average value and standard deviation,13.1.11If a specimen is rejected,reason(s)for rejection,13.1.12Tangent,secant,or chord modulus in bending,average value,standard deviation,and the strain level(s)used if secant or chord modulus,13.1.13Flexural strength (if desired),average value,and standard deviation,13.1.14Stress at any given strain up to and including 5%(if desired),with strain used,average value,and standard devia-tion,13.1.15Flexural stress at break (if desired),average value,and standard deviation,13.1.16Type of behavior,whether yielding or rupture,or both,or other observations,occurring within the 5%strain limit,and13.1.17Date of specific version of test used.TABLE 2Flexural ModulusMaterial Mean,103psiValues Expressed in units of %of 103psi V r A V R B r C R D ABS338 4.797.6913.621.8DAP thermoset 485 2.897.188.1520.4Cast acrylic 81013.716.138.845.4GR polyester816 3.49 4.209.9111.9GR polycarbonate 1790 5.52 5.5215.615.6SMC195010.913.830.839.1AV r =within-laboratory coefficient of variation for the indicated material.It is obtained by first pooling the within-laboratory standard deviations of the test results from all of the participating laboratories:Sr =[[(s 1)2+(s 2)2...+(s n )2]/n ]1/2then V r =(S r divided by the overall average for the material)3100.BV r =between-laboratory reproducibility,expressed as the coefficient of varia-tion:S R ={S r 2+S L 2}1/2where S L is the standard deviation of laboratory means.Then:V R =(S R divided by the overall average for the material)3100.Cr =within-laboratory critical interval between two test results =2.83V r .DR =between-laboratory critical interval between two test results =2.83V R.。

美国FDA食品接触材料相关检测标准

美国FDA食品接触材料相关检测标准

美国FDA食品接触材料相关检测标准
随着食品生产技术的日益多元化,食品安全问题已经不仅仅限于食品本身,还包括与食品直接或间接接触的材料。

这些材料包括食品容器、包装材料、餐厨具等,统称为食品接触材料。

由其导致的食品安全问题越来越受到社会各界的关注。

食品接触材料的测试也称为“食品级测试”。

欧盟和美国对食品接触材料管控非常严格,要求出口到欧盟及美国的产品必须通过相应的测试认证。

我国对不同的食品接触材料也有着严格的卫生要求。

因此,无论是出口或是在国内销售的食品接触材料,都必须通过相应的质量安全检测。

莱德凭借专业的技术人才及实验室,针对不同的产品类型、出口国家等,为客户提供全面的检测、认证及咨询服务。

在食品接触材料方面,我们能够为您提供以下FDA检测标准要求:
美国要求
欧盟要求
中国要求。

ASTM与国标对应项目

ASTM与国标对应项目

ASTM与国标对应项目
1、GB/T7767-2003 炭黑术语——D3053-08b
2、GB3778-2011 橡胶用炭黑标准——D1765-10
3、GB/T3780.1-2006 吸碘值测定方法——D1510-09b
4、GB/T3780.2-2007 吸油值测定方法——D2414-09a
5、GB/T3780.4-2008 压缩吸油测定方法——D3493-09
6、GB/T10722-2003 炭黑总表面积和外表面积的测定氮吸附法——D6556-09
7、GB/T3780.6-2007 着色强度测定方法——D3265-07
8、GB/T3780.7-2006 pH值测定方法——D1512-05
9、GB/T3780.8-2008 加热减量测定方法——D1509-07
10、GB/T3780.10-2009 灰分测定方法——D1506-07
11、GB/T14853.2-2006 橡胶用造粒炭黑第2部分:细粉含量的测定和粒子磨损量的测定——D1508-07
12、GB/T14853.6-2002 橡胶用造粒炭黑单个粒子破碎强度的测定——D3313-05A
13、GB/T3780.15-2006 甲苯抽出物透光率测定方法——D1618-04
14、GB/T3780.18-2007 炭黑在天然橡胶(NR)中鉴定方法——D3192-09
15、GB/T15338-2012 炭黑试验方法精密度和偏差的确认——D4821-75
16、GB/T9580-2009 标准参比炭黑的鉴定方法——D4122-06。

纺织品测试基本知识资料-2022年学习资料

纺织品测试基本知识资料-2022年学习资料

物性测试-布料组织-纱支Yarn Size-测试方法:-ASTM D1059,有定长制Direct Sys em、定重-制Indirect System-定长制Direct System:-即9600米纱,重量为1 ,称为1丹尼尔D,-此为长纤Filament纱专用。-定重制Indirect System:-Cotton CountNec或S即1磅纱其总长度为840-码,称之为1支,此为短纤Spun纱专用
纺织品测试基本概念-摄影包事业部-2019.2.16
纺织品测试可分成5方面:-物性测试Physical Testing-染色坚牢度测试Colorfastnes Tests-化学测试Chemical Testing-成份分析Fiber analysis-可燃性测试F ammability Test
物性测试-²布料组织Fabric Construction-强力特性Strength Properties 缩率Dimensional Stability
强力特性Strength Properties-断裂强力Tensile strength-撕破强力Tear ng strength-爆破强力Bursting strength-缝线滑纱Seam slippa.ge
物性测试-强力特性-断裂强力Tensile Strength-测试方法:-ASTM D5034,决定纺织物 裂强力及延伸性-重点:-此测试在提供成衣之布料经消费者使用时潜在的断裂强力-资料-限制:-不建议对针织布及 它针织布具有高弹性者(大于11%)进行-测试条件:-布料放置在恒温恒湿环境下21士1°C温度及65士2%R -相对湿度至少4小时才可进行测试-试样:4”³8”(至少4”³6”),经向及纬向皆须测试-测试机台:Ins ron-结果:布料破裂或断裂时所纪录的力量即为断裂强力

astm d257-14 固体绝缘材料体积电阻率和表面电阻率试验方法

astm d257-14 固体绝缘材料体积电阻率和表面电阻率试验方法

astm d257-14 固体绝缘材料体积电阻率和表面电阻率试验方法ASTM D257-14 是美国材料和试验协会 (American Society for Testing and Materials, ASTM) 制定的关于固体绝缘材料体积电阻率和表面电阻率的试验方法的标准。

以下是该标准的一般概述和主要步骤,但请注意具体操作步骤可能有所不同,建议具体参考标准文档以确保准确性。

ASTM D257-14 标准概述:•标题:ASTM D257-14 - Standard Test Methods for DC Resistance or Conductance of Insulating Materials •发布日期: 2014 年试验方法:1. 测试样品准备:获取符合规格的固体绝缘材料样品,确保样品的表面平整、无损伤,并符合所需的尺寸要求。

2. 测试环境:试验通常在特定的温度和湿度条件下进行,以确保结果的可比性。

温度和湿度的控制应符合标准的要求。

3. 体积电阻率测试:•使用适当的测试装置(可能是四探头体积电阻率仪),将电流引入样品,测量样品的电阻,通过计算得到体积电阻率。

•根据标准规定的电流值、电压值和测量时间,执行测试。

4. 表面电阻率测试:•使用特定电极配置,将电流引入样品的表面,测量表面电阻,通过计算得到表面电阻率。

•根据标准规定的电流值、电压值和测量时间,执行测试。

5. 数据记录与报告:记录所有测试条件、测量结果以及相关的环境参数。

按照标准的要求,报告测试结果。

6. 质量控制:根据标准的要求,执行质量控制步骤,确保测试的准确性和可重复性。

请注意,以上只是一般的概述,具体的测试步骤和要求请参考ASTM D257-14 标准文档以确保准确执行。

ASTM D类最新标准目录(一)

ASTM D类最新标准目录( 一)D4-86(2004) 沥青含量试验方法D5-06e1 沥青材料的渗透性试验方法D6-95(2000)e1 油及沥青混合物加热损失试验方法D8-02 与道路和路面材料相关的术语D9-05 与木材相关的术语D12-88(1998) 未加工的桐油D13-02 松节油规范D16-03 与涂料、清漆、亮漆和有关产品相关的术语D20-03 路面焦油的蒸馏试验方法D25-99(2005) 圆木桩D29-98 虫胶树脂的抽样和试验方法D34-91(2003) 白颜料化学分析指南D36-95(2000)e1 沥青软化点试验方法(沥青软化点测定器)D38-94(2000)e1 木材防腐剂的抽样试验方法D41-05 铺屋面、防潮及防水用沥青底层D43-00 屋顶、防潮及防水材料用杂酚油底漆D49-83(2002) 铅丹的化学分析D50-90(2005) 含铁和锰的黄色、橙色、红色和褐色涂料的化学分析试验方法D56-05 泰格密闭闪点试验器测定闪点的试验方法D61-75(2004) 硬沥青的软化点的试验方法(水中方块试验法)D69-01 磨擦带的试验方法D70-03 半固态沥青材料的比重和密度的试验方法D71-94(2004) 固体硬沥青和地沥青的相对密度试验方法(变位法)D75-03 集料的抽样D76-99(2005) 纺织材料的抗拉试验机D79-86(2004) 氧化锌颜料D81-87(2003) 碱性碳酸盐铅白颜料D83-84(2002) 铅丹颜料D85-05 赭色颜料规范D86-05 大气压下石油产品蒸馏试验方法D87-04 石蜡熔点的试验方法(冷却曲线)D88-94(2005) 赛波特粘度的试验方法D91-02 润滑油的沉淀值试验方法D92-05a 用克利夫兰德开杯法测定石油产品的闪点和燃点的试验方法D93-02a 用潘斯基-马丁斯仪闭杯闪点测定器测定闪点的试验方法D94-02 石油产品的皂化值试验方法D95-05e1 蒸馏法测定石油产品及沥青材料中水的试验方法D97-05a 石油的倾点的试验方法D98-05 氯化钙D113-99 沥青材料的延展性的试验方法D115-02 电绝缘用含清漆试验溶剂的试验方法D116-86(2006) 电气设备用上釉陶瓷材料的试验D117-02 产自石油的电绝缘油的试验方法和规范导则D120-02a 橡胶绝缘手套D121-05 煤和焦炭术语D123-03 与纺织材料相关的术语D124-88(1998) 脱胶的豆油D126-87(2002) 含铬酸铅和氧化铬绿的黄、橙和绿色颜料的化学分析方法D127-05 石油蜡包括凡士林滴熔点的试验方法D128-98(2003)e1 润滑脂分析试验方法D129-00(2005) 石油产品中硫含量试验方法(通用氧弹法)D130-04e1 用铜条变色法检测石油产品对铜腐蚀性的测试方法D139-95(2001)e1 沥青材料浮选试验的检测方法D140-01 沥青材料的抽样D143-94(2000)e1 洁净木材小样品的试验D146-04 防水与屋面材料用沥青浸渍的油毡和编织物的抽样与试验方法D149-97a(2004) 固体电绝缘材料在工业电源频率下的介电击穿电压和介电强度的试验方法D150-98(2004) 固体电绝缘材料的(恒久电介质)的交流损耗特性和介电常数的测试方法D153-84(2003) 颜料比重测试方法D154-85(2001) 清漆试验D156-02e1 石油产品赛波特比测试方法(赛波特比色计法)D167-93(2004)e1 块焦比重和孔隙度的试验方法D168-94(2000) 杂酚油焦炭渣的测试方法D173-03 屋顶和防水材料用饱和沥青棉织物D176-00 电绝缘用固体充填化合物与浸渍剂的试验方法D178-01(2005) 橡胶绝缘垫子D185-84(1999 颜料,糊剂及涂料中粗颗粒的试验方法D187-94(2003)e1 煤油燃烧质量的测试方法D189-05 石油产品康拉孙残碳测试方法D197-87(2002) 粉煤的取样方法与细度试验方法D198-05a 结构尺寸木料静力试验法D202-97(2002)e1 电绝缘用未浸渍纸的抽样和试验方法D204-02 缝线的测试方法D209-81(2003) 灯黑颜料D210-05 骨炭颜料D211-67(2002) 铬黄和铬橙颜料D215-91(2002) 白色亚麻籽油涂料的化学分析D217-02 润滑剂针入度的测试方法D225-04 表面有矿物颗粒的沥青屋面板D226-06 铺顶和防水用沥青饱和有机毡D227-03 铺顶和防水用焦油沥青饱和有机毡D228-06 沥青屋面卷材,盖板和瓦的试验方法D229-01 电绝缘用硬质薄板及板材的试验方法D233-02 松脂的抽样和测试试验方法D234-82(1998) 生亚麻子油D235-02 矿物溶剂油(石油溶液油)(烃干洗溶液)规格D237-57(1997) 橙色紫胶和其他虫胶D240-02 弹式量热器测定液烃燃料燃烧热的试验方法D242-04 沥青铺路混合料用矿物填料D243-02 规定残渣渗透性测试方法D244-04 乳化沥青的测试方法D245-06 制定目测分等木材的结构等级及有关允许性能的规程D246-04 杂酚油和杂酚油-煤焦油溶液的蒸馏试验方法D256-06 塑料及电绝缘材料的抗冲击性的测试方法D257-99(2005) 绝缘材料的直流电阻或电导的试验方法D260-86(2001) 熟亚麻籽油D261-75(1999) 铁蓝颜料D262-81(1999) 群青蓝颜料D263-05 氧化铬绿颜料D267-82(2003) 黄青铜粉规格D268-01 涂料及其相关涂层和原料用挥发性溶剂及化学中间体的抽样和测试D269-97(2002) 松香和松香衍生物中不溶物的试验方法D276-00a 纺织品中纤维的鉴定方法(AATCC方法20)D279-02 颜料渗出的试验方法D280-01 颜料吸收的水份(及试验条件下挥发的其他物质)的测试方法D281-95(2002) 用刮刀磨损法测定颜料油吸附性的试验方法D283-84(1999) 一氧化铜和铜涂料化学分析试验方法D287-92(2006) 原油和石油产品API比重的试验方法(液体比重计法)D291-86(2002) 烟煤立方英尺重量的试验方法D293-93(2004) 焦炭筛析分析试验方法D295-99(2004) 电绝缘用棉质漆布的试验方法D297-93(2002)e2 橡胶制品的测试方法.化学方法D299-04e1 石棉纱的标准规范D301-95(2004) 可溶性硝化纤维素的试验方法D304-05 n-丁醇(丁醇)D305-84(2003) 黑色涂料中的溶剂萃取材料的试验方法D312-00 屋顶用沥青D315-95(2004)e1 机织石棉带的标准规范D319-04 合成的戊醇D322-97(2002)e1 蒸馏法测定汽油发动机废机油中汽油稀释剂的试验方法D323-99a 石油产品蒸气压力的测试方法D329-02 丙酮D330-93(2001) 2-丁氧基乙醇D331-05 2-乙氧基乙醇D332-87(2004) 白色颜料着色力的试验方法D333-01 透明漆和着色漆的试验方法D341-03 液体石油产品粘度-温度关系曲线图D344-97(2004) 用擦试外规评定法对涂料相对遮盖力的测试方法D345-02 道路和结构用氯化钙的抽样和试验方法D346-04e1 实验室分析用焦炭试样的收集和制备D347-97 杂酚油和煤焦油的体积和比重修正表D348-00 电绝缘用刚性管的测试方法D349-99(2004) 电绝缘用层压圆棒的试验方法D350-01 电绝缘用经处理软套管的试验方法D351-97(2003) 天然白云母块及薄片目检质量分级D352-97(2003) 电绝缘用涂浆云母的试验方法D358-98 涂料耐大气老试验用木片规格D360-89(2001) 紫胶清漆规范D363-90(2000) 磷酸三甲苯酯规格D365-01(2005) 可溶性硝酸纤维素基溶液的试验方法D367-94(2000)e1 杂酚油中苯不溶物的测试方法D368-89(2002) 杂酚油及油质防腐剂比重的试验方法D369-84(2002) 杂酚油馏份与残渣比重的测试方法D370-02e1 油质防腐剂脱水作用的试验方法D372-00(2006) 电绝缘用经处理的软套管规格D374-99(2004) 固体电绝缘厚度的测试方法D374M-99(2005) 固体电绝缘厚度的标准测试方法(米制)D375-95(2004)e1 石棉粗砂的标准规范D378-00 平型橡胶传送带的测试方法D380-94(2006) 橡胶软管的测试方法D381-04 用喷射蒸发法测定燃烧中原在胶的测试方法D387-00 使用机械研磨机测定有色颜料主色和着力色的试验方法D388-05 用排列法测定煤的分类D390-92(1999) 海上,陆地及淡水中用木桩,电杆和木材的防腐处理用煤柏油杂酚油规程D391-94(2000)e1 杂酚油-煤焦油溶液D395-03 橡胶压缩永久变形特性的试验方法D396-05 燃料油规范D402-02 稀释沥青产品蒸馏的测试方法 Standard Test Method for Distillationof Cut-Back Asphalt ic (Bituminous) ProductsD409-02 粉碎机法测定煤炭可磨性的试验方法 Standard Test Method for Grindabilityof Coal by t he Hardgrove-Machine MethodD411-98(2003) 电绝缘用紫胶片试验方法 Standard Test Methods for ShellacUsed for Electrical I nsulationD412-98a(2002)e1 硫化橡胶、热塑橡胶和热塑合成橡胶的拉伸试验方法 Standard Test Methods f or VulcanizedRubber and Thermoplastic Elastomers—TensionD413-98(2002)e1 橡胶特性-与软质基底粘附性的试验方法 Standard Test Methods for RubberPro perty—Adhesion to Flexible SubstrateD420-98(2003) 土壤粒度分析的测试方法 Standard Guide to SiteCharacterization for Engineering, Design, and ConstructionPurposesD421-85(2002) 土壤粒度分析试验方法 Standard Practice for Dry Preparationof Soil Samples for Particle-Size Analysis and Determination ofSoil ConstantsD422-63(2002)e1 土壤粒度分析试验方法 Standard Test Method forParticle-Size Analysis of Soils D425-88(2001) 土壤离心湿度当量试验方法 Standard Test Method for CentrifugeMoisture Equiva lent of SoilsD427-04 用水银法测量土壤收缩系数的测试方法 Test Method for Shrinkage Factors ofSoils by t he Mercury MethodD429-03e1 橡胶特性与硬质基底粘附性的试验方法 Standard Test Methods for RubberProperty—Adhesion to Rigid SubstratesD430-06 橡胶变质的动态疲劳试验方法 Standard Test Methods for RubberDeterioration-Dynamic FatigueD434-95 Standard Test Method for Resistance toSlippage of Yarns in Woven Fabrics Using a St andard SeamD440-86(2002) 煤的跌落粉碎试验 Standard Test Method of Drop ShatterTest for CoalD441-86(2002) 煤的滚筒试验 Standard Test Method of Tumbler Test for CoalD444-88(2003) 锌黄颜料(铬酸锌黄)的化学分析方法 Standard Test Methods for Chemical Analysis of Zinc YellowPigment (Zinc Chromate Yellow)D445-06 透明和不透明液体运动粘度的测试方法.(包括动态粘度的计算) Standard Test Method for Kinematic Viscosity ofTransparent and Opaque Liquids (and the Calculation of DynamicViscosity)D446-06 玻璃毛细管运动粘度计操作说明书和规范 Standard Specifications and OperatingInstructi ons for Glass Capillary Kinematic ViscometersD448-03a 道路和桥梁建筑的集料尺寸分类 Standard Classification for Sizes ofAggregate for Roa d and Bridge ConstructionD449-03 防潮和防水用沥青规范 Standard Specification for AsphaltUsed in Dampproofing and WaterproofingD450-96(2006) 铺屋面,防潮与防水用硬煤沥青 Standard Specification for Coal-TarPitch Used in Roofing, Dampproofing, and WaterproofingD451-91(2002) 沥青屋顶制品用粒状矿物铺面材料筛分分析试验方法 Standard Test Method for Si eveAnalysis of Granular Mineral Surfacing For Asphalt RoofingProductsD452-91(2002) 沥青层面制品表面修整用非粒状矿物的筛分试验方法 Standard Test Method for Si eveAnalysis of Surfacing for Asphalt Roofing ProductsD453-94(2000)e1 杂酚油-煤焦油溶液中焦油酸含量的测试方法 Standard Test Method for Tar Aci ds inCreosote-Coal Tar SolutionsD454-04 用加热及空气压力测定橡胶变质的试验方法 Standard Test Method for RubberDeteriorat ion by Heat and Air PressureD459-00 肥皂和其它洗涤剂的术语规范 Standard Terminology Relating toSoaps and Other Deter gentsD460-91(2005) 肥皂和其它洗涤剂粒度的试验方法 Standard Test Methods for Samplingand Che mical Analysis of Soaps and Soap ProductsD464-05 松脂油产品包括妥尔油和其他相关产品的皂化值的试验方法 Standard Test Methods for Saponification Number of Naval Store Products Including Tall Oil and Other Related ProductsD465-05 松脂制品包括妥尔油及其它相关产品酸值的试验方法 Standard Test Methods for Acid N umberof Naval Stores Products Including Tall Oil and Other RelatedProductsD470-05 电线和电缆用交联绝缘与套管的测试方法 Standard Test Methods for CrosslinkedInsulati ons and Jackets for Wire and CableD471-98e2 液体对橡胶性能影响的测试方法 Standard Test Method for RubberProperty-Effect of LiquidsD473-02 萃取法测定原油和燃料油中沉积物的试验方法 Standard Test Method for Sediment inCr ude Oils and Fuel Oils by the Extraction MethodD476-00(2005) 二氧化钛颜料规范 Standard Classification for DryPigmentary Titanium Dioxide P roductsD478-02 锌黄(铬酸锌)颜料 Standard Specificationfor Zinc Yellow (Zinc Chromate) PigmentsD480-88(2003) 铝粉和铝粉浆的抽样和试验方法 Standard Test Methods for Samplingand Testin g of Flaked Aluminum Powders and PastesD482-03 石油产品灰分的测试方法 Standard Test Method for Ash fromPetroleum ProductsD483-04 石油制植物喷洒油不磺化残渣的试验方法 Standard Test Method for UnsulfonatedResidu e of Petroleum Plant Spray OilsD490-92(2005) 道路柏油 Standard Specification for Road TarD494-04 Standard Test Method for Acetone Extraction ofPhenolic Molded or Laminated Products Standard TestMethod for Acetone Extraction of Phenolic Molded or LaminatedProductsD495-99(2004) 固体电绝缘材料的耐高压低电流干电弧性能的测试方法 Standard Test Method for High-Voltage, Low-Current, Dry Arc Resistance of Solid ElectricalInsulationD500-95(2003) 磺化油和硫化油的化学分析和试验方法D501-03 碱性洗涤剂的抽样和化学分析试验方法D502-89(2003) 肥皂和其它洗涤剂粒度的试验方法D509-05 松香分级和抽样试验方法D511-03 水中钙镁离子的测试方法D512-04 测定水中氯离子含量的试验方法D513-02 水中二氧化碳溶解量和总量的试验方法D516-02 水中硫酸铁的试验方法D517-98(2003) 沥青厚板材D518-99 橡胶变质表面龟裂的试验方法D519-04 羊毛条中纤维长度的试验方法D520-00(2005) 锌粉颜料规范D521-02 锌粉(金属锌粉)的化学分析试验方法D522-93a(2001) 用锥形心轴仪测定涂覆有机涂层延伸率的试验方法D523-89(1999) 镜面光泽的试验方法D524-04 石油产品中兰氏残炭的试验方向D525-05 汽油氧化稳定性的试验方法(诱导期方法)D528-97(2002) 纸和纸板的机器定向试验方向D529-04 沥青材料的加速风化试验条件和程序的测试方法(碳弧法)D531-00(2005) 普西和琼斯橡胶压缩试验方法D542-00 透明有机塑料的折射指数的试验方法D543-06 塑料耐化学试剂性能的试验方法D545-99(2005) 混凝土用预制伸缩缝纫填料的试验方法(非挤压和弹性型)D546-05 道路和铺砌材料用矿物填料筛分的测试方法D548-97(2002) 纸张水溶解酸碱度的试验方法D555-84(1998) 干性油试验D558-04 土壤水泥混合物的水分与密度关系的试验方法D559-03 压实的掺土水泥混合物的湿润与干燥的试验方法D560-03 压实的掺土水泥混合物的冻融试验方法D561-82(2003) 涂料用炭黑颜料D562-01(2005) 斯氏粘度计测定涂料稠度的试验方法D563-88(1996)e1 醇酸树脂和树脂溶液中苯酐含量的试验方法D564-87(2002) 液体涂料催干剂的试验方法D565-99(2005) 白色矿物油中可碳化物质的试验方法D566-02 润滑脂滴点的试验方法D570-98(2005) 塑料吸水率的试验方法D572-04 用加热法和氧化法进行的橡胶变质的试验方法D573-04 在空气烤炉中作橡胶变质的试验方法D575-91(2001) 橡胶压缩特性的试验方法D578-05 玻璃纤维丝D579-04 原织物玻璃纤维D580-04 机织玻璃纤维带D581-99 机织玻璃纤维套管的编织D584-96(2005) 原毛中羊毛含量实验室测试方法D585-97(2002) 纸张、纸板、纤维板和相关产品的单批取样和验收方法D586-97(2002) 纸中灰分含量的试验方法D589-97(2002) 纸的不透明度的测试方法D590-93(2002) 纸中石油蜡的测试方法D596-01 水分析结果的报告D600-90(2001) 液体涂料催干剂D601-87(1998) 奥气油(永久液体)D602-81(2003) 硫酸钡颜料规范D605-82(2003) 硅酸镁颜料(滑石)D607-82(2003) 湿磨云母颜料D608-05 邻苯二甲酸二丁酯D609-00 涂料、油漆以及改性涂料与相关涂料产品的测试用冷轧钢板的制备D610-01 涂漆钢表面锈蚀程度评价的试验方法D611-04 石油产品和烃类溶剂苯胺点和混合苯胺点的试验方法D612-88(2004) 石蜡中可碳化物质的试验方法D613-05 十六烷法测定柴油燃料燃烧质量的试验方法D618-05 塑料及电绝缘材料的调理方法D619-99(2004) 电绝缘用硫化纤维的测试方法D622-99(2005) 汽车空气制动和真空制动系统用橡胶软管试验方法D623-99e1 橡胶特性-压缩中热的产生及挠曲疲劳的试验方法D624-00e1 橡胶的热塑性弹性的耐老化性的抗撕裂强度的试验方法D628-95(2004)e1 石棉套管的标准规范D629-99 纺织品定量分析试验方法D632-01 氯化钠D633-97(2005) 道路柏油的体积修正表D635-06 自承塑料在水平状态时的燃烧速率或者燃烧蔓延程度及燃烧时间的试验方法D638-03 塑料拉伸性能的试验方法D642-00(2005) 船用集装箱、组合件和单体加载的抗压缩能力的测试方法D643-97(2002) 用厦泊测试仪测试纸的折痕持久性的标准试验方法D644-99(2002) 用烘干法测定纸和纸板中水分的测试方法D645/D645M-97(2002) 纸和纸板厚度的测试方法D646-96(2001) 纸张及纸板的基本重量的试验方法(单位面积的重量)D648-06 在挠曲负荷下塑料的挠曲温度的试验方法D653-05 土壤、岩石和其内部所含液体的相关术语D660-93(2005) 外用漆龟裂程度评价方法D661-93(2005) 外用漆破裂程度评价的试验方法D662-93(2005) 外用漆侵蚀程度评价的试验方法D664-06 电位滴定法测定石油产品酸值的试验方法D665-06 水存在下抑制的矿物油防锈特性的试验方法D668-99(2004) 电绝缘用硬条和硬管尺度测量的测试方法D669-03 层压薄板与层压板的平行于层片的耗散系数和介电常数的试验方法D685-93(2002) 检测调理纸和纸制品D686-93(2002) 纸中矿物填料和矿物涂料的定性测试方法D689-03 纸张的内部耐撕裂的试验方法D692-00(2004) 沥青铺路砌混合用粗集料D693-03a 碎石路面用压碎集料D695-02a 硬质塑料抗压特性的试验方法D696-03 从-30摄氏度到30摄氏度的塑料线性热膨胀系数的试验方法D698-00ae1 实验室中用12000ft-lbt/ft(600KN-m/m)作用力测定土壤压力特性的试验方法D704-99(2004) 三氯氰胺甲醛模制化合物D705-99(2004) 脲甲醛模制化合物D706-05 乙酸纤维素模制和挤压化合物D707-05 醋酸丁酸纤维素模制与挤压料规格D709-01 层压热固材料D710-97(2002) 电绝缘用硫化纤维薄板、条和管D711-89(2004) 路标漆不粘着时间的试验方法D713-90(2004) 路标漆进行路面使用的试验方法D714-02e1 涂料起泡程度的试验方法D715-86(2003) 硫酸钡颜料分析的标准试验方法D716-86(2003) 评定云母颜料的标准试验方法D717-86(2003) 硅酸镁颜料分析的标准试验方法D718-86(2003) 硅酸铝颜料的分析标准试验方法D720-91(2004)e1 煤自由膨胀指数的试验方法D721-05 石油蜡含油量的试验方法D722-93(2002) 纸的抗油脂性标准试验方法D724-99(2003) 纸表面可湿性的测试方法(接触角法)D726-94(2003) 空气中无孔纸的透气性的测试方法D727-96(2001) 真空方法测定屋顶和地板油毡煤油值的试验方法D731-95(1999) 热固模塑料粉末的模塑指数的试验方法D732-02 用穿孔工具测量塑料剪切强度的测试方法D737-04 纺织纤维透气率的试验方法D740-05 丁酮规范D746-04 用冲击法测定塑料及弹性材料的脆化温度的试验方法D747-02 用悬臂梁法对塑料表观弯曲系数的测试方法D748-00(2005)e1 固定式云母介电电容器用天然云母块和云母薄片D750-00 用碳弧型装置和风化装置对橡胶变质的测试方法D751-06 涂层织物的测试方法D763-01 未加工棕土和焙烧棕土颜料D765-87(2003) 未加工黄土和焙烧黄土颜料技术规范D768-01 黄色氧化铁的水合物D769-01 黑色合成氧化铁D770-05 异丙醇规范D772-86(2005) 外部涂料剂落程度评价的试验方法D774/D774M-97(2002) 纸张抗破碎强度的测试方法D776-92(2001) 干热对纸和纸板特性的影响的试验方法D777-97(2002) 经过处理的纸和纸板易燃性的标准试验方法D778-97(2002) 纸萃液(热萃取和冷萃取法)氢离子浓度(pH)的标准试验方法D779-03 纸、纸板和其他印刷材料用干烧指示器法测试耐水性的测试方法D780-95(2003) 纸印刷油墨渗透性的测试方法(蓖麻油试验)D784-03 电绝缘材料用橙色紫胶和其他印度虫胶D785-03 塑料和电绝缘材料的洛氏硬度的测试方法D787-96(2003) 乙基纤维模制和挤压化合物D788-05 甲基丙烯酸酯模制和挤压化合物的分类系统D789-06 聚酰胺相对粘度,熔点和含水量的测试方法D790-03 未增强和增强塑料及电绝缘材料的挠曲性的试验方法D792-00 用位移法测定塑料密度和比重(相对密度)的标准试验方法D800-05 工业用金属除垢剂化学分析试验方法D801-02 二聚戊烯抽样和测试的试验方法D802-02 松油抽样和测试的试验方法D803-03 妥儿油的测试试验方法D804-02 松脂制品包括妥儿油及相关产品的术语D806-00(2006) 掺土水泥混合物中水泥含量的试验方法D807-05 工业锅炉用水引起脆裂倾向的评价方法(美国矿业局的脆变检查器方法)D808-05 新的和使用过的石油产品中氯含量的试验方法(氧弹法)D813-06 测定橡胶龟裂扩展的试验方法D814-95(2005) 橡胶特性挥发性液体蒸汽渗透性的试验方法D816-06 橡胶胶水的试验方法D817-96(2004) 乙酸丙酸纤维素和醋酸丁酸纤维素的试验方法D820-93(2003) 含合成洗涤剂肥皂的化学分析试验方法D822-01 用经过过滤明光碳弧灯和水中曝光装置对涂料及相关涂层和材料上做的导电试验D823-95(2001) 色漆,清漆,喷漆及有关产品制成厚度均匀漆膜试片的方法D824-94(2002) 用皱文纸测定吸水率的测试方法D828-97(2002) 纸和纸板拉力破坏强度的测试方法D829-97(2002) 纸和纸制品湿抗拉断裂强度的标准试验方法D831-94(2004) 电缆及电容器油的气体含量的测试方法D832-92(2001)e1 低温状态下的橡胶试验D841-02 甲苯的硝化定级D843-06 硝化二甲苯D847-04 苯,甲苯,二甲苯,溶剂石脑油和类似的工业芳烃酸度的试验方法D848-03 工业芳烃的酸洗颜色的标准试验方法D849-05 工业芳烃对铜条腐蚀的标准试验方法D850-03 工业芳轻及相关物质的蒸溜法D852-02 苯凝固点的试验方法D853-04 工业芳烃中硫化氢和二氧化硫含量(定性)的标准试验方法D854-06 土壤比重的试验方法D857-02 水中铝含量的测试方法D858-02 水中锰含量的试验方法D859-05 水中二氧化硅的测试方法D861-01a 用特克斯制命名纤维,纱的半制品,纱和其它纺织品线度D865-99(2005) 橡胶的空气中加热变质试验方法(试管法)D866-99(2004) 电线及电缆用丁苯合成橡胶套D868-85(2003) 路标漆渗色程度评价的试验方法D869-85(2004) 涂漆沉降程度评价试验方法D870-02 水浸渍法涂层耐水试验D871-96(2004) 测试乙酸纤维素的试验方法D873-02 航空燃料的氧化稳定性的测试方法D874-06 润滑油和添加剂中硫酸盐类灰分的测试方法D876-00 电绝缘用刚性氧化乙烯聚合物管的测试方法D877-02e1 用圆盘电极测定电绝缘液体介电击穿电压的试验方法D878-01e1 绝缘油中无机氯化物和硫酸盐的测试方法D880-92(2002) 船用集装箱的冲击试验的试验方法D882-02 塑料薄板材抗拉特性的试验方法D883-00 塑料相关术语D885-06 由人造有机纤维制成的轮胎帘子线,轮胎帘布和工业长纱线的测试D887-82(2003)e1 水沉积物抽样D888-05 水中溶解氧的试验方法D889-99(2004) 松香中油挥发性的试验方法D890-98(2003) 液体松脂中水含量的试验方法D891-95(2004) 液态工业化合物的比重,表观比重的测试方法D892-05 润滑油发泡特性的标准试验方法D893-05a 用过的润滑油中不溶物的试验方法D896-04 胶粘剂耐化学试剂粘法的试验方法D897-01e1 胶粘剂粘结力的抗拉性的测试方法D898-05 胶粘剂固体单位面积涂用重量的试验方法D899-00 单位面积涂用液体胶粘剂的重量的测试方法D902-00 电绝缘用挠性涂树脂玻璃布和玻璃布带的测试方法D903-98(2004) 胶粘剂粘结抗剥落或爆皮强度的试验方法D904-99(2005) 人造光(碳弧型)和自然光对胶粘剂试样的曝光D905-03 用压缩荷载法测定胶粘剂的抗剪切强度性能的试验方法D906-98(2004) 用拉力负荷法测定胶合板结构中胶粘剂剪切强度特性的试验方法D907-05e1 胶粘剂术语D909-01e1 增压进料法测定航空汽油抗震性的试验方法(联邦试验方法No.791b) D910-04a 航空汽油技术规范D912-81(1999) 防污涂料用氧化亚铜D913-03e1 路标漆耐磨程度的评价方法D914-00(2006) 乙基纤维的试验方法D918-99(2003) 纸和纸板的抗粘结性试验方法D919-97(2002) 纸和纸板的铜值测试方法D922-00a(2006) 非硬质聚氯乙烯管D923-97 电绝缘液体的抽样方法D924-04 电绝缘液体的损耗因数(或功率因数)和介电常数(电容率)的测试方法D925-06 橡胶特性.表面着色(接触、色移和扩散)的试验方法D926-04 用平行板法测量橡胶的塑性和弹性D928-03 碳酸氢钠D932-85(2002) 水和水沉积物中嗜铁细菌含量试验方法D933-84(2003) 水沉积物的检验和分析结果的报告方法D934-80(2003) 用X射线衍射法作水沉积物中结晶化合物的识别方法D937-04 石油脂的针入度试验方法D938-05 石油蜡(包括凡士林)凝固点的测试方法D942-02 氧弹法测定润滑脂氧化稳定性的试验方法D943-04a 防腐蚀矿物油氧化特性的试验方法D945-06 用机械示波器测定在压缩应力和剪切应力下橡胶特性的试验方法D946-82(2005) 路面建造用按贯入度级配的沥青膏D950-03 胶粘剂抗冲击强度的试验方法D951-99(2004) 用喷射法测定船运集装箱的耐水性的试验方法D952-02 薄板塑料和电绝缘材料粘结强度的试验方法D953-02 塑料支承强度的测试方法D955-00 模制塑料模型尺寸收缩率的测量方法D957-95(2006)e1 塑料生产用模型表面温度的测定D960-02a 生蓖麻油D961-86(2001) 脱水蓖麻油D962-81(2003) 涂料用铝粉和铝浆颜料D964-03 防污漆用铜粉D968-05 用落沙磨蚀法测定有机涂层耐磨性的试验方法D969-85(2003) 路标漆渗色程度的实验室试验方法D971-99a(2004) 环法测定油水界面张力的试验方法D972-02 润滑脂和润滑油蒸发损失的测试方法D974-04 用颜色指示剂滴定法测定酸碱值的标准试验方法D975-06 柴油技术规范D976-04be1 馏分燃料正十六烷指数的计算方法D977-05 乳化沥青D979-01(2006)e1 沥青铺面混合料的取样方法D982-05 Standard Test Method for Organic Nitrogen in Paper andPaperboard D984-97(2002)。

(完整版)ASTMD257-07中文版绝缘材料直流电阻和电导测试.…

ASTM D257-07 中文版绝缘材料直流电阻和电导测试.…ASTMD绝缘材料直流电阻或电导的标准试验方法本标准是以固定代号D发布的。

其后的数字表示原文本正式通过的年号在有修订的情况下为上一次的修订年号圆括号中数字为上一次重新确认的年号。

上标符号(ε)表示对上次修改或重新确定的版本有编辑上的修改。

本标准经批准用于国防部所有机构。

1.范围本试验方法包含直流绝缘电阻体积电阻和表面电阻的测量所用直流程序。

通过该测量及样本和电极的几何尺寸可以计算出电绝缘材料的体积电阻和表面电阻同时还可以计算出相应的电导和电导率。

这些试验方法不适用于测量中等导电材料的电阻电导。

这些材料评估可采用试验方法D4496。

本标准描述了几种可选择的测量电阻(或电导)的普通方法。

特殊材料科采用最合适的标准ASTM试验方法进行测试这些特殊材料具有电压应力范围和有限起电时间同时规定了样本结构和电极几何形状。

这些个别特殊试验方法将能更好得定义测量值的精度和偏差。

本试验方法包括以下章节:试验方法或步骤章节计算13设备和试验方法的选择7清洗固体样本10.1 样本的状态调节11屏蔽电极的有效面积附录X2电极系 6绝缘电阻或电导材料的影响因素附录X1湿度控制11.2 液体样本和电池9.4精度和偏差15 电阻或电导测量步骤12 引用文件 2 报告14 抽样8 重要性和用途 5 样本安装10 试验方法摘要 4 术语 3 绝缘电阻体积电阻和表面电阻或电导测量用试验样本9 典型测量方法附录X3本标准并没有完全列举所有的安全声明如果有必要根据实际使用情况进行斟酌。

使用本规范前使用者有责任制定符合安全和健康要求的条例和规范并明确该规范的使用范围。

引用文件ASTM标准:D150固体电绝缘材料的(恒久电介质)的交流损耗特性和介电常数的测试方法D374固体电绝缘材料厚度的标准试验方法D1169电绝缘液电阻率(电阻系数)试验方法D1711电绝缘相关术语D4496中等导电材料直流电阻或导电性的标准试验方法D5032用水甘油溶液设备维持恒定相关湿度的规程D6054测试用电工绝缘材料的调节规程E104用水溶液保持相对恒定湿度的标准实施规程术语定义:以下定义直接来自术语标准D1711适用于本标准正文所用术语。

美国橡胶检验标准系列号

ASTM D3896-2007
合成橡胶取样的标准实施规范.取样
Standard Practice for Rubber From Synthetic Sources8212;Sampling
ASTM D624-2000(2007)
传统硫化橡胶和热塑性弹性体的撕裂强度的标准试验方法
Standard Test Method for Tear Strength of Conventional Vulcanized Rubber and Thermoplastic Elastomers
ASTM D1646-2007
橡胶粘度、应力松驰及预硫化特性(穆尼粘度计)的标准试验方法
Standard Test Methods for Rubber-Viscosity, Stress Relaxation, and Pre-Vulcanization Characteristics (Mooney Viscometer)
ASTM D5775-1995(2009)
SBR中合成来源的苯乙烯橡胶的标准试验方法
Standard Test Method for Rubber from Synthetic Sources-Bound Styrene in SBR
ASTM D6814-2002(2008)
基于交联点密度的粒状生胶脱硫百分比测定的标准试验方法
用无转子硫化仪测量橡胶性能硫化的标准试验方法
Standard Test Method for Rubber Property-Vulcanization Using Rotorless Cure Meters
ASTM D2433-2007
橡胶线的标准试验方法
Standard Test Methods for Rubber Thread

(完整版)ASTMD类最新标准目录(一)

ASTM D类最新标准目录( 一)D4-86(2004) 沥青含量试验方法D5-06e1 沥青材料的渗透性试验方法D6-95(2000)e1 油及沥青混合物加热损失试验方法D8-02 与道路和路面材料相关的术语D9-05 与木材相关的术语D12-88(1998) 未加工的桐油D13-02 松节油规范D16-03 与涂料、清漆、亮漆和有关产品相关的术语D20-03 路面焦油的蒸馏试验方法D25-99(2005) 圆木桩D29-98 虫胶树脂的抽样和试验方法D34-91(2003) 白颜料化学分析指南D36-95(2000)e1 沥青软化点试验方法(沥青软化点测定器)D38-94(2000)e1 木材防腐剂的抽样试验方法D41-05 铺屋面、防潮及防水用沥青底层D43-00 屋顶、防潮及防水材料用杂酚油底漆D49-83(2002) 铅丹的化学分析D50-90(2005) 含铁和锰的黄色、橙色、红色和褐色涂料的化学分析试验方法D56-05 泰格密闭闪点试验器测定闪点的试验方法D61-75(2004) 硬沥青的软化点的试验方法(水中方块试验法)D69-01 磨擦带的试验方法D70-03 半固态沥青材料的比重和密度的试验方法D71-94(2004) 固体硬沥青和地沥青的相对密度试验方法(变位法)D75-03 集料的抽样D76-99(2005) 纺织材料的抗拉试验机D79-86(2004) 氧化锌颜料D81-87(2003) 碱性碳酸盐铅白颜料D83-84(2002) 铅丹颜料D85-05 赭色颜料规范D86-05 大气压下石油产品蒸馏试验方法D87-04 石蜡熔点的试验方法(冷却曲线)D88-94(2005) 赛波特粘度的试验方法D91-02 润滑油的沉淀值试验方法D92-05a 用克利夫兰德开杯法测定石油产品的闪点和燃点的试验方法D93-02a 用潘斯基-马丁斯仪闭杯闪点测定器测定闪点的试验方法D94-02 石油产品的皂化值试验方法D95-05e1 蒸馏法测定石油产品及沥青材料中水的试验方法D97-05a 石油的倾点的试验方法D98-05 氯化钙D113-99 沥青材料的延展性的试验方法D115-02 电绝缘用含清漆试验溶剂的试验方法D116-86(2006) 电气设备用上釉陶瓷材料的试验D117-02 产自石油的电绝缘油的试验方法和规范导则D120-02a 橡胶绝缘手套D121-05 煤和焦炭术语D123-03 与纺织材料相关的术语D124-88(1998) 脱胶的豆油D126-87(2002) 含铬酸铅和氧化铬绿的黄、橙和绿色颜料的化学分析方法D127-05 石油蜡包括凡士林滴熔点的试验方法D128-98(2003)e1 润滑脂分析试验方法D129-00(2005) 石油产品中硫含量试验方法(通用氧弹法)D130-04e1 用铜条变色法检测石油产品对铜腐蚀性的测试方法D139-95(2001)e1 沥青材料浮选试验的检测方法D140-01 沥青材料的抽样D143-94(2000)e1 洁净木材小样品的试验D146-04 防水与屋面材料用沥青浸渍的油毡和编织物的抽样与试验方法D149-97a(2004) 固体电绝缘材料在工业电源频率下的介电击穿电压和介电强度的试验方法D150-98(2004) 固体电绝缘材料的(恒久电介质)的交流损耗特性和介电常数的测试方法D153-84(2003) 颜料比重测试方法D154-85(2001) 清漆试验D156-02e1 石油产品赛波特比测试方法(赛波特比色计法)D167-93(2004)e1 块焦比重和孔隙度的试验方法D168-94(2000) 杂酚油焦炭渣的测试方法D173-03 屋顶和防水材料用饱和沥青棉织物D176-00 电绝缘用固体充填化合物与浸渍剂的试验方法D178-01(2005) 橡胶绝缘垫子D185-84(1999 颜料,糊剂及涂料中粗颗粒的试验方法D187-94(2003)e1 煤油燃烧质量的测试方法D189-05 石油产品康拉孙残碳测试方法D197-87(2002) 粉煤的取样方法与细度试验方法D198-05a 结构尺寸木料静力试验法D202-97(2002)e1 电绝缘用未浸渍纸的抽样和试验方法D204-02 缝线的测试方法D209-81(2003) 灯黑颜料D210-05 骨炭颜料D211-67(2002) 铬黄和铬橙颜料D215-91(2002) 白色亚麻籽油涂料的化学分析D217-02 润滑剂针入度的测试方法D225-04 表面有矿物颗粒的沥青屋面板D226-06 铺顶和防水用沥青饱和有机毡D227-03 铺顶和防水用焦油沥青饱和有机毡D228-06 沥青屋面卷材,盖板和瓦的试验方法D229-01 电绝缘用硬质薄板及板材的试验方法D233-02 松脂的抽样和测试试验方法D234-82(1998) 生亚麻子油D235-02 矿物溶剂油(石油溶液油)(烃干洗溶液)规格D237-57(1997) 橙色紫胶和其他虫胶D240-02 弹式量热器测定液烃燃料燃烧热的试验方法D242-04 沥青铺路混合料用矿物填料D243-02 规定残渣渗透性测试方法D244-04 乳化沥青的测试方法D245-06 制定目测分等木材的结构等级及有关允许性能的规程D246-04 杂酚油和杂酚油-煤焦油溶液的蒸馏试验方法D256-06 塑料及电绝缘材料的抗冲击性的测试方法D257-99(2005) 绝缘材料的直流电阻或电导的试验方法D260-86(2001) 熟亚麻籽油D261-75(1999) 铁蓝颜料D262-81(1999) 群青蓝颜料D263-05 氧化铬绿颜料D267-82(2003) 黄青铜粉规格D268-01 涂料及其相关涂层和原料用挥发性溶剂及化学中间体的抽样和测试D269-97(2002) 松香和松香衍生物中不溶物的试验方法D276-00a 纺织品中纤维的鉴定方法(AATCC方法20)D279-02 颜料渗出的试验方法D280-01 颜料吸收的水份(及试验条件下挥发的其他物质)的测试方法D281-95(2002) 用刮刀磨损法测定颜料油吸附性的试验方法D283-84(1999) 一氧化铜和铜涂料化学分析试验方法D287-92(2006) 原油和石油产品API比重的试验方法(液体比重计法)D291-86(2002) 烟煤立方英尺重量的试验方法D293-93(2004) 焦炭筛析分析试验方法D295-99(2004) 电绝缘用棉质漆布的试验方法D297-93(2002)e2 橡胶制品的测试方法.化学方法D299-04e1 石棉纱的标准规范D301-95(2004) 可溶性硝化纤维素的试验方法D304-05 n-丁醇(丁醇)D305-84(2003) 黑色涂料中的溶剂萃取材料的试验方法D312-00 屋顶用沥青D315-95(2004)e1 机织石棉带的标准规范D319-04 合成的戊醇D322-97(2002)e1 蒸馏法测定汽油发动机废机油中汽油稀释剂的试验方法D323-99a 石油产品蒸气压力的测试方法D329-02 丙酮D330-93(2001) 2-丁氧基乙醇D331-05 2-乙氧基乙醇D332-87(2004) 白色颜料着色力的试验方法D333-01 透明漆和着色漆的试验方法D341-03 液体石油产品粘度-温度关系曲线图D344-97(2004) 用擦试外规评定法对涂料相对遮盖力的测试方法D345-02 道路和结构用氯化钙的抽样和试验方法D346-04e1 实验室分析用焦炭试样的收集和制备D347-97 杂酚油和煤焦油的体积和比重修正表D348-00 电绝缘用刚性管的测试方法D349-99(2004) 电绝缘用层压圆棒的试验方法D350-01 电绝缘用经处理软套管的试验方法D351-97(2003) 天然白云母块及薄片目检质量分级D352-97(2003) 电绝缘用涂浆云母的试验方法D358-98 涂料耐大气老试验用木片规格D360-89(2001) 紫胶清漆规范D363-90(2000) 磷酸三甲苯酯规格D365-01(2005) 可溶性硝酸纤维素基溶液的试验方法D367-94(2000)e1 杂酚油中苯不溶物的测试方法D368-89(2002) 杂酚油及油质防腐剂比重的试验方法D369-84(2002) 杂酚油馏份与残渣比重的测试方法D370-02e1 油质防腐剂脱水作用的试验方法D372-00(2006) 电绝缘用经处理的软套管规格D374-99(2004) 固体电绝缘厚度的测试方法D374M-99(2005) 固体电绝缘厚度的标准测试方法(米制)D375-95(2004)e1 石棉粗砂的标准规范D378-00 平型橡胶传送带的测试方法D380-94(2006) 橡胶软管的测试方法D381-04 用喷射蒸发法测定燃烧中原在胶的测试方法D387-00 使用机械研磨机测定有色颜料主色和着力色的试验方法D388-05 用排列法测定煤的分类D390-92(1999) 海上,陆地及淡水中用木桩,电杆和木材的防腐处理用煤柏油杂酚油规程D391-94(2000)e1 杂酚油-煤焦油溶液D395-03 橡胶压缩永久变形特性的试验方法D396-05 燃料油规范D402-02 稀释沥青产品蒸馏的测试方法 Standard Test Method for Distillationof Cut-Back Asphalt ic (Bituminous) ProductsD409-02 粉碎机法测定煤炭可磨性的试验方法 Standard Test Method for Grindabilityof Coal by t he Hardgrove-Machine MethodD411-98(2003) 电绝缘用紫胶片试验方法 Standard Test Methods for ShellacUsed for Electrical I nsulationD412-98a(2002)e1 硫化橡胶、热塑橡胶和热塑合成橡胶的拉伸试验方法 Standard Test Methods f or VulcanizedRubber and Thermoplastic Elastomers—TensionD413-98(2002)e1 橡胶特性-与软质基底粘附性的试验方法 Standard Test Methods for RubberPro perty—Adhesion to Flexible SubstrateD420-98(2003) 土壤粒度分析的测试方法 Standard Guide to SiteCharacterization for Engineering, Design, and ConstructionPurposesD421-85(2002) 土壤粒度分析试验方法 Standard Practice for Dry Preparationof Soil Samples for Particle-Size Analysis and Determination ofSoil ConstantsD422-63(2002)e1 土壤粒度分析试验方法 Standard Test Method forParticle-Size Analysis of Soils D425-88(2001) 土壤离心湿度当量试验方法 Standard Test Method for CentrifugeMoisture Equiva lent of SoilsD427-04 用水银法测量土壤收缩系数的测试方法 Test Method for Shrinkage Factors ofSoils by t he Mercury MethodD429-03e1 橡胶特性与硬质基底粘附性的试验方法 Standard Test Methods for RubberProperty—Adhesion to Rigid SubstratesD430-06 橡胶变质的动态疲劳试验方法 Standard Test Methods for RubberDeterioration-Dynamic FatigueD434-95 Standard Test Method for Resistance toSlippage of Yarns in Woven Fabrics Using a St andard SeamD440-86(2002) 煤的跌落粉碎试验 Standard Test Method of Drop ShatterTest for CoalD441-86(2002) 煤的滚筒试验 Standard Test Method of Tumbler Test for CoalD444-88(2003) 锌黄颜料(铬酸锌黄)的化学分析方法 Standard Test Methods for Chemical Analysis of Zinc YellowPigment (Zinc Chromate Yellow)D445-06 透明和不透明液体运动粘度的测试方法.(包括动态粘度的计算) Standard Test Method for Kinematic Viscosity ofTransparent and Opaque Liquids (and the Calculation of DynamicViscosity)D446-06 玻璃毛细管运动粘度计操作说明书和规范 Standard Specifications and OperatingInstructi ons for Glass Capillary Kinematic ViscometersD448-03a 道路和桥梁建筑的集料尺寸分类 Standard Classification for Sizes ofAggregate for Roa d and Bridge ConstructionD449-03 防潮和防水用沥青规范 Standard Specification for AsphaltUsed in Dampproofing and WaterproofingD450-96(2006) 铺屋面,防潮与防水用硬煤沥青 Standard Specification for Coal-TarPitch Used in Roofing, Dampproofing, and WaterproofingD451-91(2002) 沥青屋顶制品用粒状矿物铺面材料筛分分析试验方法 Standard Test Method for Si eveAnalysis of Granular Mineral Surfacing For Asphalt RoofingProductsD452-91(2002) 沥青层面制品表面修整用非粒状矿物的筛分试验方法 Standard Test Method for Si eveAnalysis of Surfacing for Asphalt Roofing ProductsD453-94(2000)e1 杂酚油-煤焦油溶液中焦油酸含量的测试方法 Standard Test Method for Tar Aci ds inCreosote-Coal Tar SolutionsD454-04 用加热及空气压力测定橡胶变质的试验方法 Standard Test Method for RubberDeteriorat ion by Heat and Air PressureD459-00 肥皂和其它洗涤剂的术语规范 Standard Terminology Relating toSoaps and Other Deter gentsD460-91(2005) 肥皂和其它洗涤剂粒度的试验方法 Standard Test Methods for Samplingand Che mical Analysis of Soaps and Soap ProductsD464-05 松脂油产品包括妥尔油和其他相关产品的皂化值的试验方法 Standard Test Methods for Saponification Number of Naval Store Products Including Tall Oil and Other Related ProductsD465-05 松脂制品包括妥尔油及其它相关产品酸值的试验方法 Standard Test Methods for Acid N umberof Naval Stores Products Including Tall Oil and Other RelatedProductsD470-05 电线和电缆用交联绝缘与套管的测试方法 Standard Test Methods for CrosslinkedInsulati ons and Jackets for Wire and CableD471-98e2 液体对橡胶性能影响的测试方法 Standard Test Method for RubberProperty-Effect of LiquidsD473-02 萃取法测定原油和燃料油中沉积物的试验方法 Standard Test Method for Sediment inCr ude Oils and Fuel Oils by the Extraction MethodD476-00(2005) 二氧化钛颜料规范 Standard Classification for DryPigmentary Titanium Dioxide P roductsD478-02 锌黄(铬酸锌)颜料 Standard Specificationfor Zinc Yellow (Zinc Chromate) PigmentsD480-88(2003) 铝粉和铝粉浆的抽样和试验方法 Standard Test Methods for Samplingand Testin g of Flaked Aluminum Powders and PastesD482-03 石油产品灰分的测试方法 Standard Test Method for Ash fromPetroleum ProductsD483-04 石油制植物喷洒油不磺化残渣的试验方法 Standard Test Method for UnsulfonatedResidu e of Petroleum Plant Spray OilsD490-92(2005) 道路柏油 Standard Specification for Road TarD494-04 Standard Test Method for Acetone Extraction ofPhenolic Molded or Laminated Products Standard TestMethod for Acetone Extraction of Phenolic Molded or LaminatedProductsD495-99(2004) 固体电绝缘材料的耐高压低电流干电弧性能的测试方法 Standard Test Method for High-Voltage, Low-Current, Dry Arc Resistance of Solid ElectricalInsulationD500-95(2003) 磺化油和硫化油的化学分析和试验方法D501-03 碱性洗涤剂的抽样和化学分析试验方法D502-89(2003) 肥皂和其它洗涤剂粒度的试验方法D509-05 松香分级和抽样试验方法D511-03 水中钙镁离子的测试方法D512-04 测定水中氯离子含量的试验方法D513-02 水中二氧化碳溶解量和总量的试验方法D516-02 水中硫酸铁的试验方法D517-98(2003) 沥青厚板材D518-99 橡胶变质表面龟裂的试验方法D519-04 羊毛条中纤维长度的试验方法D520-00(2005) 锌粉颜料规范D521-02 锌粉(金属锌粉)的化学分析试验方法D522-93a(2001) 用锥形心轴仪测定涂覆有机涂层延伸率的试验方法D523-89(1999) 镜面光泽的试验方法D524-04 石油产品中兰氏残炭的试验方向D525-05 汽油氧化稳定性的试验方法(诱导期方法)D528-97(2002) 纸和纸板的机器定向试验方向D529-04 沥青材料的加速风化试验条件和程序的测试方法(碳弧法)D531-00(2005) 普西和琼斯橡胶压缩试验方法D542-00 透明有机塑料的折射指数的试验方法D543-06 塑料耐化学试剂性能的试验方法D545-99(2005) 混凝土用预制伸缩缝纫填料的试验方法(非挤压和弹性型)D546-05 道路和铺砌材料用矿物填料筛分的测试方法D548-97(2002) 纸张水溶解酸碱度的试验方法D555-84(1998) 干性油试验D558-04 土壤水泥混合物的水分与密度关系的试验方法D559-03 压实的掺土水泥混合物的湿润与干燥的试验方法D560-03 压实的掺土水泥混合物的冻融试验方法D561-82(2003) 涂料用炭黑颜料D562-01(2005) 斯氏粘度计测定涂料稠度的试验方法D563-88(1996)e1 醇酸树脂和树脂溶液中苯酐含量的试验方法D564-87(2002) 液体涂料催干剂的试验方法D565-99(2005) 白色矿物油中可碳化物质的试验方法D566-02 润滑脂滴点的试验方法D570-98(2005) 塑料吸水率的试验方法D572-04 用加热法和氧化法进行的橡胶变质的试验方法D573-04 在空气烤炉中作橡胶变质的试验方法D575-91(2001) 橡胶压缩特性的试验方法D578-05 玻璃纤维丝D579-04 原织物玻璃纤维D580-04 机织玻璃纤维带D581-99 机织玻璃纤维套管的编织D584-96(2005) 原毛中羊毛含量实验室测试方法D585-97(2002) 纸张、纸板、纤维板和相关产品的单批取样和验收方法D586-97(2002) 纸中灰分含量的试验方法D589-97(2002) 纸的不透明度的测试方法D590-93(2002) 纸中石油蜡的测试方法D596-01 水分析结果的报告D600-90(2001) 液体涂料催干剂D601-87(1998) 奥气油(永久液体)D602-81(2003) 硫酸钡颜料规范D605-82(2003) 硅酸镁颜料(滑石)D607-82(2003) 湿磨云母颜料D608-05 邻苯二甲酸二丁酯D609-00 涂料、油漆以及改性涂料与相关涂料产品的测试用冷轧钢板的制备D610-01 涂漆钢表面锈蚀程度评价的试验方法D611-04 石油产品和烃类溶剂苯胺点和混合苯胺点的试验方法D612-88(2004) 石蜡中可碳化物质的试验方法D613-05 十六烷法测定柴油燃料燃烧质量的试验方法D618-05 塑料及电绝缘材料的调理方法D619-99(2004) 电绝缘用硫化纤维的测试方法D622-99(2005) 汽车空气制动和真空制动系统用橡胶软管试验方法D623-99e1 橡胶特性-压缩中热的产生及挠曲疲劳的试验方法D624-00e1 橡胶的热塑性弹性的耐老化性的抗撕裂强度的试验方法D628-95(2004)e1 石棉套管的标准规范D629-99 纺织品定量分析试验方法D632-01 氯化钠D633-97(2005) 道路柏油的体积修正表D635-06 自承塑料在水平状态时的燃烧速率或者燃烧蔓延程度及燃烧时间的试验方法D638-03 塑料拉伸性能的试验方法D642-00(2005) 船用集装箱、组合件和单体加载的抗压缩能力的测试方法D643-97(2002) 用厦泊测试仪测试纸的折痕持久性的标准试验方法D644-99(2002) 用烘干法测定纸和纸板中水分的测试方法D645/D645M-97(2002) 纸和纸板厚度的测试方法D646-96(2001) 纸张及纸板的基本重量的试验方法(单位面积的重量)D648-06 在挠曲负荷下塑料的挠曲温度的试验方法D653-05 土壤、岩石和其内部所含液体的相关术语D660-93(2005) 外用漆龟裂程度评价方法D661-93(2005) 外用漆破裂程度评价的试验方法D662-93(2005) 外用漆侵蚀程度评价的试验方法D664-06 电位滴定法测定石油产品酸值的试验方法D665-06 水存在下抑制的矿物油防锈特性的试验方法D668-99(2004) 电绝缘用硬条和硬管尺度测量的测试方法D669-03 层压薄板与层压板的平行于层片的耗散系数和介电常数的试验方法D685-93(2002) 检测调理纸和纸制品D686-93(2002) 纸中矿物填料和矿物涂料的定性测试方法D689-03 纸张的内部耐撕裂的试验方法D692-00(2004) 沥青铺路砌混合用粗集料D693-03a 碎石路面用压碎集料D695-02a 硬质塑料抗压特性的试验方法D696-03 从-30摄氏度到30摄氏度的塑料线性热膨胀系数的试验方法D698-00ae1 实验室中用12000ft-lbt/ft(600KN-m/m)作用力测定土壤压力特性的试验方法D704-99(2004) 三氯氰胺甲醛模制化合物D705-99(2004) 脲甲醛模制化合物D706-05 乙酸纤维素模制和挤压化合物D707-05 醋酸丁酸纤维素模制与挤压料规格D709-01 层压热固材料D710-97(2002) 电绝缘用硫化纤维薄板、条和管D711-89(2004) 路标漆不粘着时间的试验方法D713-90(2004) 路标漆进行路面使用的试验方法D714-02e1 涂料起泡程度的试验方法D715-86(2003) 硫酸钡颜料分析的标准试验方法D716-86(2003) 评定云母颜料的标准试验方法D717-86(2003) 硅酸镁颜料分析的标准试验方法D718-86(2003) 硅酸铝颜料的分析标准试验方法D720-91(2004)e1 煤自由膨胀指数的试验方法D721-05 石油蜡含油量的试验方法D722-93(2002) 纸的抗油脂性标准试验方法D724-99(2003) 纸表面可湿性的测试方法(接触角法)D726-94(2003) 空气中无孔纸的透气性的测试方法D727-96(2001) 真空方法测定屋顶和地板油毡煤油值的试验方法D731-95(1999) 热固模塑料粉末的模塑指数的试验方法D732-02 用穿孔工具测量塑料剪切强度的测试方法D737-04 纺织纤维透气率的试验方法D740-05 丁酮规范D746-04 用冲击法测定塑料及弹性材料的脆化温度的试验方法D747-02 用悬臂梁法对塑料表观弯曲系数的测试方法D748-00(2005)e1 固定式云母介电电容器用天然云母块和云母薄片D750-00 用碳弧型装置和风化装置对橡胶变质的测试方法D751-06 涂层织物的测试方法D763-01 未加工棕土和焙烧棕土颜料D765-87(2003) 未加工黄土和焙烧黄土颜料技术规范D768-01 黄色氧化铁的水合物D769-01 黑色合成氧化铁D770-05 异丙醇规范D772-86(2005) 外部涂料剂落程度评价的试验方法D774/D774M-97(2002) 纸张抗破碎强度的测试方法D776-92(2001) 干热对纸和纸板特性的影响的试验方法D777-97(2002) 经过处理的纸和纸板易燃性的标准试验方法D778-97(2002) 纸萃液(热萃取和冷萃取法)氢离子浓度(pH)的标准试验方法D779-03 纸、纸板和其他印刷材料用干烧指示器法测试耐水性的测试方法D780-95(2003) 纸印刷油墨渗透性的测试方法(蓖麻油试验)D784-03 电绝缘材料用橙色紫胶和其他印度虫胶D785-03 塑料和电绝缘材料的洛氏硬度的测试方法D787-96(2003) 乙基纤维模制和挤压化合物D788-05 甲基丙烯酸酯模制和挤压化合物的分类系统D789-06 聚酰胺相对粘度,熔点和含水量的测试方法D790-03 未增强和增强塑料及电绝缘材料的挠曲性的试验方法D792-00 用位移法测定塑料密度和比重(相对密度)的标准试验方法D800-05 工业用金属除垢剂化学分析试验方法D801-02 二聚戊烯抽样和测试的试验方法D802-02 松油抽样和测试的试验方法D803-03 妥儿油的测试试验方法D804-02 松脂制品包括妥儿油及相关产品的术语D806-00(2006) 掺土水泥混合物中水泥含量的试验方法D807-05 工业锅炉用水引起脆裂倾向的评价方法(美国矿业局的脆变检查器方法)D808-05 新的和使用过的石油产品中氯含量的试验方法(氧弹法)D813-06 测定橡胶龟裂扩展的试验方法D814-95(2005) 橡胶特性挥发性液体蒸汽渗透性的试验方法D816-06 橡胶胶水的试验方法D817-96(2004) 乙酸丙酸纤维素和醋酸丁酸纤维素的试验方法D820-93(2003) 含合成洗涤剂肥皂的化学分析试验方法D822-01 用经过过滤明光碳弧灯和水中曝光装置对涂料及相关涂层和材料上做的导电试验D823-95(2001) 色漆,清漆,喷漆及有关产品制成厚度均匀漆膜试片的方法D824-94(2002) 用皱文纸测定吸水率的测试方法D828-97(2002) 纸和纸板拉力破坏强度的测试方法D829-97(2002) 纸和纸制品湿抗拉断裂强度的标准试验方法D831-94(2004) 电缆及电容器油的气体含量的测试方法D832-92(2001)e1 低温状态下的橡胶试验D841-02 甲苯的硝化定级D843-06 硝化二甲苯D847-04 苯,甲苯,二甲苯,溶剂石脑油和类似的工业芳烃酸度的试验方法D848-03 工业芳烃的酸洗颜色的标准试验方法D849-05 工业芳烃对铜条腐蚀的标准试验方法D850-03 工业芳轻及相关物质的蒸溜法D852-02 苯凝固点的试验方法D853-04 工业芳烃中硫化氢和二氧化硫含量(定性)的标准试验方法D854-06 土壤比重的试验方法D857-02 水中铝含量的测试方法D858-02 水中锰含量的试验方法D859-05 水中二氧化硅的测试方法D861-01a 用特克斯制命名纤维,纱的半制品,纱和其它纺织品线度D865-99(2005) 橡胶的空气中加热变质试验方法(试管法)D866-99(2004) 电线及电缆用丁苯合成橡胶套D868-85(2003) 路标漆渗色程度评价的试验方法D869-85(2004) 涂漆沉降程度评价试验方法D870-02 水浸渍法涂层耐水试验D871-96(2004) 测试乙酸纤维素的试验方法D873-02 航空燃料的氧化稳定性的测试方法D874-06 润滑油和添加剂中硫酸盐类灰分的测试方法D876-00 电绝缘用刚性氧化乙烯聚合物管的测试方法D877-02e1 用圆盘电极测定电绝缘液体介电击穿电压的试验方法D878-01e1 绝缘油中无机氯化物和硫酸盐的测试方法D880-92(2002) 船用集装箱的冲击试验的试验方法D882-02 塑料薄板材抗拉特性的试验方法D883-00 塑料相关术语D885-06 由人造有机纤维制成的轮胎帘子线,轮胎帘布和工业长纱线的测试D887-82(2003)e1 水沉积物抽样D888-05 水中溶解氧的试验方法D889-99(2004) 松香中油挥发性的试验方法D890-98(2003) 液体松脂中水含量的试验方法D891-95(2004) 液态工业化合物的比重,表观比重的测试方法D892-05 润滑油发泡特性的标准试验方法D893-05a 用过的润滑油中不溶物的试验方法D896-04 胶粘剂耐化学试剂粘法的试验方法D897-01e1 胶粘剂粘结力的抗拉性的测试方法D898-05 胶粘剂固体单位面积涂用重量的试验方法D899-00 单位面积涂用液体胶粘剂的重量的测试方法D902-00 电绝缘用挠性涂树脂玻璃布和玻璃布带的测试方法D903-98(2004) 胶粘剂粘结抗剥落或爆皮强度的试验方法D904-99(2005) 人造光(碳弧型)和自然光对胶粘剂试样的曝光D905-03 用压缩荷载法测定胶粘剂的抗剪切强度性能的试验方法D906-98(2004) 用拉力负荷法测定胶合板结构中胶粘剂剪切强度特性的试验方法D907-05e1 胶粘剂术语D909-01e1 增压进料法测定航空汽油抗震性的试验方法(联邦试验方法No.791b) D910-04a 航空汽油技术规范D912-81(1999) 防污涂料用氧化亚铜D913-03e1 路标漆耐磨程度的评价方法D914-00(2006) 乙基纤维的试验方法D918-99(2003) 纸和纸板的抗粘结性试验方法D919-97(2002) 纸和纸板的铜值测试方法D922-00a(2006) 非硬质聚氯乙烯管D923-97 电绝缘液体的抽样方法D924-04 电绝缘液体的损耗因数(或功率因数)和介电常数(电容率)的测试方法D925-06 橡胶特性.表面着色(接触、色移和扩散)的试验方法D926-04 用平行板法测量橡胶的塑性和弹性D928-03 碳酸氢钠D932-85(2002) 水和水沉积物中嗜铁细菌含量试验方法D933-84(2003) 水沉积物的检验和分析结果的报告方法D934-80(2003) 用X射线衍射法作水沉积物中结晶化合物的识别方法D937-04 石油脂的针入度试验方法D938-05 石油蜡(包括凡士林)凝固点的测试方法D942-02 氧弹法测定润滑脂氧化稳定性的试验方法D943-04a 防腐蚀矿物油氧化特性的试验方法D945-06 用机械示波器测定在压缩应力和剪切应力下橡胶特性的试验方法D946-82(2005) 路面建造用按贯入度级配的沥青膏D950-03 胶粘剂抗冲击强度的试验方法D951-99(2004) 用喷射法测定船运集装箱的耐水性的试验方法D952-02 薄板塑料和电绝缘材料粘结强度的试验方法D953-02 塑料支承强度的测试方法D955-00 模制塑料模型尺寸收缩率的测量方法D957-95(2006)e1 塑料生产用模型表面温度的测定D960-02a 生蓖麻油D961-86(2001) 脱水蓖麻油D962-81(2003) 涂料用铝粉和铝浆颜料D964-03 防污漆用铜粉D968-05 用落沙磨蚀法测定有机涂层耐磨性的试验方法D969-85(2003) 路标漆渗色程度的实验室试验方法D971-99a(2004) 环法测定油水界面张力的试验方法D972-02 润滑脂和润滑油蒸发损失的测试方法D974-04 用颜色指示剂滴定法测定酸碱值的标准试验方法D975-06 柴油技术规范D976-04be1 馏分燃料正十六烷指数的计算方法D977-05 乳化沥青D979-01(2006)e1 沥青铺面混合料的取样方法D982-05 Standard Test Method for Organic Nitrogen in Paper andPaperboard D984-97(2002)。

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Designation:D257–07An American National StandardStandard Test Methods forDC Resistance or Conductance of Insulating Materials1This standard is issued under thefixed designation D257;the number immediately following the designation indicates 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(e)indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1.Scope*1.1These test methods cover direct-current procedures forthe measurement of dc insulation resistance,volume resistance,and surface resistance.From such measurements and thegeometric dimensions of specimen and electrodes,both vol-ume and surface resistivity of electrical insulating materialscan be calculated,as well as the corresponding conductancesand conductivities.1.2These test methods are not suitable for use in measuringthe electrical resistance/conductance of moderately conductivee Test Method D4496to evaluate such materials.1.3This standard describes several general alternativemethodologies for measuring resistance(or conductance).Specific materials can be tested most appropriately by usingstandard ASTM test methods applicable to the specific materialthat define both voltage stress limits andfinite electrificationtimes as well as specimen configuration and electrode geom-etry.These individual specific test methodologies would bebetter able to define the precision and bias for the determina-tion.1.4The procedures appear in the following sections:Test Method or Procedure SectionCalculation13Choice of Apparatus and Test Method7Cleaning Solid Specimens10.1Conditioning of Specimens11Effective Area of Guarded Electrode AppendixX2Electrode Systems6Factors Affecting Insulation Resistance or Conductance Measurements Appendix X1Humidity Control11.2 Liquid Specimens and Cells9.4 Precision and Bias15 Procedure for the Measurement of Resist-ance or Conductance12 Referenced Documents2 Report14 Sampling8 Significance and Use5 Specimen Mounting10 Summary of Test Methods4Terminology3Test Specimens for Insulation,Volume,and SurfaceResistance or Conductance Determination9Typical Measurement Methods AppendixX31.5This standard does not purport to address all of the safety concerns,if any,associated with its use.It is the responsibility 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 Documents2.1ASTM Standards:2D150Test Methods for AC Loss Characteristics and Per-mittivity(Dielectric Constant)of Solid Electrical Insula-tionD374Test Methods for Thickness of Solid Electrical Insu-lationD1169Test Method for Specific Resistance(Resistivity)of Electrical Insulating LiquidsD1711Terminology Relating to Electrical InsulationD4496Test Method for D-C Resistance or Conductance of Moderately Conductive MaterialsD5032Practice for Maintaining Constant Relative Humid-ity by Means of Aqueous Glycerin SolutionsD6054Practice for Conditioning Electrical Insulating Ma-terials for TestingE104Practice for Maintaining Constant Relative Humidity by Means of Aqueous Solutions3.Terminology3.1Definitions—The following definitions are taken from Terminology D1711and apply to the terms used in the text of this standard.3.1.1conductance,insulation,n—the ratio of the total volume and surface current between two electrodes(on or in a specimen)to the dc voltage applied to the two electrodes. 3.1.1.1Discussion—Insulation conductance is the recipro-cal of insulation resistance.1These test methods are under the jurisdiction of ASTM Committee D09onElectrical and Electronic Insulating Materials and are the direct responsibility of Subcommittee D09.12on Electrical Tests.Current edition approved May15,2007.Published June2007.Originally approved st previous edition approved in2005as D257–99(2005).2For referenced ASTM standards,visit the ASTM website,,or contact ASTM Customer Service at service@.For Annual Book of ASTM Standards volume information,refer to the standard’s Document Summary page on the ASTM website.*A Summary of Changes section appears at the end of this standard. Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States. --`,,```,,,,````-`-`,,`,,`,`,,`---3.1.2conductance,surface,n—the ratio of the current between two electrodes(on the surface of a specimen)to the dc voltage applied to the electrodes.3.1.2.1Discussion—(Some volume conductance is un-avoidably included in the actual measurement.)Surface con-ductance is the reciprocal of surface resistance.3.1.3conductance,volume,n—the ratio of the current in the volume of a specimen between two electrodes(on or in the specimen)to the dc voltage applied to the two electrodes. 3.1.3.1Discussion—V olume conductance is the reciprocal of volume resistance.3.1.4conductivity,surface,n—the surface conductance multiplied by that ratio of specimen surface dimensions(dis-tance between electrodes divided by the width of electrodes defining the current path)which transforms the measured conductance to that obtained if the electrodes had formed the opposite sides of a square.3.1.4.1Discussion—Surface conductivity is expressed in siemens.It is popularly expressed as siemens/square(the size of the square is immaterial).Surface conductivity is the reciprocal of surface resistivity.3.1.5conductivity,volume,n—the volume conductance multiplied by that ratio of specimen volume dimensions (distance between electrodes divided by the cross-sectional area of the electrodes)which transforms the measured conduc-tance to that conductance obtained if the electrodes had formed the opposite sides of a unit cube.3.1.5.1Discussion—V olume conductivity is usually ex-pressed in siemens/centimetre or in siemens/metre and is the reciprocal of volume resistivity.3.1.6moderately conductive,adj—describes a solid mate-rial having a volume resistivity between1and10000000 V-cm.3.1.7resistance,insulation,(R i),n—the ratio of the dc voltage applied to two electrodes(on or in a specimen)to the total volume and surface current between them.3.1.7.1Discussion—Insulation resistance is the reciprocal of insulation conductance.3.1.8resistance,surface,(R s),n—the ratio of the dc voltage applied to two electrodes(on the surface of a specimen)to the current between them.3.1.8.1Discussion—(Some volume resistance is unavoid-ably included in the actual measurement.)Surface resistance is the reciprocal of surface conductance.3.1.9resistance,volume,(R v),n—the ratio of the dc voltage applied to two electrodes(on or in a specimen)to the current in the volume of the specimen between the electrodes.3.1.9.1Discussion—V olume resistance is the reciprocal of volume conductance.3.1.10resistivity,surface,(r s),n—the surface resistance multiplied by that ratio of specimen surface dimensions(width of electrodes defining the current path divided by the distance between electrodes)which transforms the measured resistance to that obtained if the electrodes had formed the opposite sides of a square.3.1.10.1Discussion—Surface resistivity is expressed in ohms.It is popularly expressed also as ohms/square(the size of the square is immaterial).Surface resistivity is the reciprocal of surface conductivity.3.1.11resistivity,volume,(r v),n—the volume resistance multiplied by that ratio of specimen volume dimensions (cross-sectional area of the specimen between the electrodes divided by the distance between electrodes)which transforms the measured resistance to that resistance obtained if the electrodes had formed the opposite sides of a unit cube.3.1.11.1Discussion—Volume resistivity is usually ex-pressed in ohm-centimetres(preferred)or in ohm-metres. V olume resistivity is the reciprocal of volume conductivity.4.Summary of Test Methods4.1The resistance or conductance of a material specimen or of a capacitor is determined from a measurement of current or of voltage drop under specified conditions.By using the appropriate electrode systems,surface and volume resistance or conductance may be measured separately.The resistivity or conductivity can then be calculated when the required speci-men and electrode dimensions are known.5.Significance and Use5.1Insulating materials are used to isolate components of an electrical system from each other and from ground,as well as to provide mechanical support for the components.For this purpose,it is generally desirable to have the insulation resis-tance as high as possible,consistent with acceptable mechani-cal,chemical,and heat-resisting properties.Since insulation resistance or conductance combines both volume and surface resistance or conductance,its measured value is most useful when the test specimen and electrodes have the same form as is required in actual use.Surface resistance or conductance changes rapidly with humidity,while volume resistance or conductance changes slowly although thefinal change may eventually be greater.5.2Resistivity or conductivity may be used to predict, indirectly,the low-frequency dielectric breakdown and dissi-pation factor properties of some materials.Resistivity or conductivity is often used as an indirect measure of:moisture content,degree of cure,mechanical continuity,or deterioration of various types.The usefulness of these indirect measure-ments is dependent on the degree of correlation established by supporting theoretical or experimental investigations.A de-crease of surface resistance may result either in an increase of the dielectric breakdown voltage because the electricfield intensity is reduced,or a decrease of the dielectric breakdown voltage because the area under stress is increased.5.3All the dielectric resistances or conductances depend on the length of time of electrification and on the value of applied voltage(in addition to the usual environmental variables). These must be known and reported to make the measured value of resistance or conductance meaningful.Within the electrical insulation materials industry,the adjective“apparent”is gen-erally applied to resistivity values obtained under conditions of arbitrarily selected electrification time.See X1.4.5.4V olume resistivity or conductivity can be calculated from resistance and dimensional data for use as an aidin --` , , ` ` ` , , , , ` ` ` ` -` -` , , ` , , ` , ` , , ` ---designing an insulator for a specific application.The change of resistivity or conductivity with temperature and humidity may be great(1,2,3,4),3and must be known when designing for operating conditions.V olume resistivity or conductivity deter-minations are often used in checking the uniformity of an insulating material,either with regard to processing or to detect conductive impurities that affect the quality of the material and that may not be readily detectable by other methods.5.5V olume resistivities above1021V·cm(1019V·m),cal-culated from data obtained on specimens tested under usual laboratory conditions,are of doubtful validity,considering the limitations of commonly used measuring equipment.5.6Surface resistance or conductance cannot be measured accurately,only approximated,because some degree of volume resistance or conductance is always involved in the measure-ment.The measured value is also affected by the surface contamination.Surface contamination,and its rate of accumu-lation,is affected by many factors including electrostatic charging and interfacial tension.These,in turn,may affect the surface resistivity.Surface resistivity or conductivity can be considered to be related to material properties when contami-nation is involved but is not a material property of electrical insulation material in the usual sense.6.Electrode Systems6.1The electrodes for insulating materials should be of a material that is readily applied,allows intimate contact with the specimen surface,and introduces no appreciable error because of electrode resistance or contamination of the specimen(5). The electrode material should be corrosion-resistant under the conditions of test.For tests of fabricated specimens such as feed-through bushings,cables,etc.,the electrodes employed are a part of the specimen or its mounting.Measurements of insulation resistance or conductance,then,include the contami-nating effects of electrode or mounting materials and are generally related to the performance of the specimen in actual use.6.1.1Binding-Post and Taper-Pin Electrodes,Fig.1and Fig.2,provide a means of applying voltage to rigid insulating materials to permit an evaluation of their resistive or conduc-tive properties.These electrodes simulate to some degree the actual conditions of use,such as binding posts on instrument panels and terminal strips.In the case of laminated insulating materials having high-resin-content surfaces,somewhat lower insulation resistance values may be obtained with taper-pin than with binding posts,due to more intimate contact with the body of the insulating material.Resistance or conductancevalues obtained are highly influenced by the individual contact between each pin and the dielectric material,the surface roughness of the pins,and the smoothness of the hole in the dielectric material.Reproducibility of results on different specimens is difficult to obtain.6.1.2Metal Bars in the arrangement of Fig.3were prima-rily devised to evaluate the insulation resistance or conduc-tance offlexible tapes and thin,solid specimens as a fairly simple and convenient means of electrical quality control.This arrangement is somewhat more satisfactory for obtaining approximate values of surface resistance or conductance when the width of the insulating material is much greater than its thickness.3The boldface numbers in parentheses refer to the list of references appended to these testmethods.FIG.1Binding-Post Electrodes for Flat,SolidSpecimensFIG.2Taper-PinElectrodes--`,,```,,,,````-`-`,,`,,`,`,,`---6.1.3Silver Paint ,Fig.4,Fig.5,and Fig.6,is available commercially with a high conductivity,either air-drying or low-temperature-baking varieties,which are sufficiently po-rous to permit diffusion of moisture through them and thereby allow the test specimen to be conditioned after the application of the electrodes.This is a particularly useful feature in studying resistance-humidity effects,as well as change with temperature.However,before conductive paint is used as an electrode material,it should be established that the solvent in the paint does not attack the material so as to change itselectrical properties.Reasonably smooth edges of guard elec-trodes may be obtained with a fine-bristle brush.However,for circular electrodes,sharper edges can be obtained by the use of a ruling compass and silver paint for drawing the outline circles of the electrodes and filling in the enclosed areas by brush.A narrow strip of masking tape may be used,provided the pressure-sensitive adhesive used does not contaminate the surface of the specimen.Clamp-on masks also may be used if the electrode paint is sprayed on.6.1.4Sprayed Metal ,Fig.4,Fig.5,and Fig.6,may be used if satisfactory adhesion to the test specimen can be obtained.Thin sprayed electrodes may have certain advantages in that they are ready for use as soon as applied.They may be sufficiently porous to allow the specimen to be conditioned,but this should be verified.Narrow strips of masking tape or clamp-on masks must be used to produce a gap between the guarded and the guard e a tape that is known not to contaminate the gap surface.6.1.5Evaporated Metal may be used under the same con-ditions given in 6.1.4.6.1.6Metal Foil ,Fig.4,may be applied to specimen surfaces as electrodes.The usual thickness of metal foil used for resistance or conductance studies of dielectrics ranges from 6to 80µm.Lead or tin foil is in most common use,and is usually attached to the test specimen by a minimum quantity of petrolatum,silicone grease,oil,or other suitable material,as an adhesive.Such electrodes shall be applied under a smoothing pressure sufficient to eliminate all wrinkles,and to work excess adhesive toward the edge of the foil where it can be wiped off with a cleansing tissue.One very effective method is to use a hard narrow roller (10to 15mm wide),and to roll outward on the surface until no visible imprint can be made on the foil with the roller.This technique can be used satisfactorily only on specimens that have very flat surfaces.With care,the adhesive film can be reduced to 2.5µm.As this film is in series withtheFIG.3Strip Electrodes for Tapes and Flat,SolidSpecimensFIG.4Flat Specimen for Measuring Volume and SurfaceResistances orConductancesFIG.5Tubular Specimen for Measuring Volume and SurfaceResistances orConductancesspecimen,it will always cause the measured resistance to be too high.This error may become excessive for the lower-resistivity specimens of thickness less than 250µm.Also the hard roller can force sharp particles into or through thin films (50µm).Foil electrodes are not porous and will not allow the test specimen to condition after the electrodes have been applied.The adhesive may lose its effectiveness at elevated temperatures necessitating the use of flat metal back-up plates under pressure.It is possible,with the aid of a suitable cutting device,to cut a proper width strip from one electrode to form a guarded and guard electrode.Such a three-terminal specimen normally cannot be used for surface resistance or conductance measurements because of the grease remaining on the gap surface.It may be very difficult to clean the entire gap surface without disturbing the adjacent edges of the electrode.6.1.7Colloidal Graphite ,Fig.4,dispersed in water or other suitable vehicle,may be brushed on nonporous,sheet insulat-ing materials to form an air-drying electrode.Masking tapes or clamp-on masks may be used (6.1.4).This electrode material is recommended only if all of the following conditions are met:6.1.7.1The material to be tested must accept a graphite coating that will not flake before testing,6.1.7.2The material being tested must not absorb water readily,and6.1.7.3Conditioning must be in a dry atmosphere (Proce-dure B,Practice D 6054),and measurements made in this same atmosphere.6.1.8Liquid metal electrodes give satisfactory results and may prove to be the best method to achieving the contact to the specimen necessary for effective resistance measurements.The liquid metal forming the upper electrodes should be confined by stainless steel rings,each of which should have its lower rimreduced to a sharp edge by beveling on the side away from the liquid metal.Fig.7and Fig.8show two possible electrode arrangements.6.1.9Flat Metal Plates ,Fig.4,(preferably guarded)may be used for testing flexible and compressible materials,both at room temperature and at elevated temperatures.They may be circular or rectangular (for tapes).To ensure intimate contact with the specimen,considerable pressure is usuallyrequired.FIG.6Conducting-PaintElectrodesFIG.7Liquid Metal Electrodes for Flat,SolidSpecimens--`,,```,,,,````-`-`,,`,,`,`,,`---Pressures of 140to 700kPa have been found satisfactory (see material specifications).6.1.9.1A variation of flat metal plate electrode systems is found in certain cell designs used to measure greases or filling compounds.Such cells are preassembled and the material to be tested is either added to the cell between fixed electrodes or the electrodes are forced into the material to a predetermined electrode spacing.Because the configuration of the electrodes in these cells is such that the effective electrode area and the distance between them is difficult to measure,each cell constant,K ,(equivalent to the A/t factor from Table 1)can be derived from the following equation:K 53.6p C 511.3C(1)where:K has units of centimetres,andC has units of picofarads and is the capacitance of the electrode system withair as the dielectric.See Test Methods D 150for methods of measurement for C.6.1.10Conducting Rubber has been used as electrode ma-terial,as in Fig.4,and has the advantage that it can quickly and easily be applied and removed from the specimen.As the electrodes are applied only during the time of measurement,they do not interfere with the conditioning of the specimen.The conductive-rubber material must be backed by proper plates and be soft enough so that effective contact with the specimen is obtained when a reasonable pressure is applied.N OTE 1—There is evidence that values of conductivity obtained using conductive-rubber electrodes are always smaller (20to 70%)than values obtained with tinfoil electrodes (6).When only order-of-magnitude accuracies are required,and these contact errors can be neglected,a properly designed set of conductive-rubber electrodes can provide a rapid means for making conductivity and resistivity determinations.6.1.11Water is widely employed as one electrode in testing insulation on wires and cables.Both ends of the specimen mustbe out of the water and of such length that leakage along the insulation is negligible.Refer to specific wire and cable test methods for the necessity to use guard at each end of a specimen.For standardization it is desirable to add sodium chloride to the water so as to produce a sodium chloride concentration of 1.0to 1.1%NaCl to ensure adequate conduc-tivity.Measurements at temperatures up to about 100°C have been reported as feasible.7.Choice of Apparatus and Test Method7.1Power Supply —A source of very steady direct voltage is required (see X1.7.3).Batteries or other stable direct voltage supplies have been proven suitable for use.7.2Guard Circuit —Whether measuring resistance of an insulating material with two electrodes (no guard)or with a three-terminal system (two electrodes plus guard),consider how the electrical connections are made between the test instrument and the test specimen.If the test specimen is at some distance from the test instrument,or the test specimen is tested under humid conditions,or if a relatively high (1010to 1015ohms)specimen resistance is expected,spurious resis-tance paths can easily exist between the test instrument and test specimen.A guard circuit is necessary to minimize interference from these spurious paths (see also X1.9).7.2.1With Guard Electrode —Use coaxial cable,with the core lead to the guarded electrode and the shield to the guard electrode,to make adequate guarded connections between the test equipment and test specimen.Coaxial cable (again with the shield tied back to the guard)for the unguarded lead is not mandatory here (or in 7.2.2),although its use provides some reduction in background noise (see also Fig.9).7.2.2Without Guard Electrode —Use coaxial cable,with the core lead to one electrode and the shield terminated about 1cm from the end of the core lead (see also Fig.10).7.3Direct Measurements —The current through a specimen at a fixed voltage is measured using any equipment that has the required sensitivity and accuracy (610%is usually adequate).Current-measuring devices available include electrometers,d-c amplifiers with indicating meters,and galvanometers.Typical methods and circuits are given in Appendix X3.When the measuring device scale is calibrated to read ohms directly no calculations are required for resistance measurements.7.4Comparison Methods —A Wheatstone-bridge circuit may be used to compare the resistance of the specimen with that of a standard resistor (see Appendix X3).7.5Precision and Bias Considerations :7.5.1General —As a guide in the choice of apparatus,the pertinent considerations are summarized in Table 2,but it is not implied that the examples enumerated are the only ones applicable.This table is not intended to indicate the limits of sensitivity and error of the various methods per se ,but rather is intended to indicate limits that are distinctly possible with modern apparatus.In any case,such limits can be achieved or exceeded only through careful selection and combination of the apparatus employed.It must be emphasized,however,that the errors considered are those of instrumentation only.Errors such as those discussed in Appendix X1are an entirely different matter.In this latter connection,the last column of Table 2lists the resistance that is shunted by the insulationresistanceFIG.8Liquid Metal Cell for Thin SheetMaterial--`,,```,,,,````-`-`,,`,,`,`,,`---between the guarded electrode and the guard system for the various methods.In general,the lower such resistance,the less probability of error from undue shunting.N OTE2—No matter what measurement method is employed,the highest precisions are achieved only with careful evaluation of all sources of error.It is possible either to set up any of these methods from the component parts,or to acquire a completely integrated apparatus.In general,the methods using high-sensitivity galvanometers require a more permanent installation than those using indicating meters or recorders.The methods using indicating devices such as voltmeters,galvanometers,d-c amplifiers,and electrometers require the minimum of manual adjustment and are easy to read but the operator is required to make the reading at a particular time.The Wheatstone bridge(Fig.X1.4)and the potentiometer method(Fig.X1.2(b))require the undivided attention of the operator in keeping a balance,but allow the setting at a particular time to be read at leisure.7.5.2Direct Measurements:7.5.2.1Galvanometer-Voltmeter—The maximum percent-age error in the measurement of resistance by the galvanometer-voltmeter method is the sum of the percentage errors of galvanometer indication,galvanometer readability, and voltmeter indication.As an example:a galvanometer having a sensitivity of500pA/scale division will be deflected 25divisions with500V applied to a resistance of40G V (conductance of25pS).If the deflection can be read to the nearest0.5division,and the calibration error(including Ayrton Shunt error)is62%of the observed value,the resultant galvanometer error will not exceed64%.If the voltmeter has an error of62%of full scale,this resistance can be measured with a maximum error of66%when the voltmeter reads full scale,and610%when it reads one-third full scale.The desirability of readings near full scale are readily apparent.7.5.2.2Voltmeter-Ammeter—The maximum percentage er-ror in the computed value is the sum of the percentage errors in the voltages,V x and V s,and the resistance,R s.The errors in V s and R s are generally dependent more on the characteristicsTABLE1Calculation of Resistivity or Conductivity AA All dimensions are in centimetres.of the apparatus used than on the particular method.The most significant factors that determine the errors in V s are indicator errors,amplifier zero drift,and amplifier gain stability.Withmodern,well-designed amplifiers or electrometers,gain stabil-ity is usually not a matter of concern.With existing techniques,the zero drift of direct voltage amplifiers or electrometers cannot be eliminated but it can be made slow enough to be relatively insignificant for these measurements.The zero drift is virtually nonexistent for carefully designed converter-type amplifiers.Consequently,the null method of Fig.X1.2(b )is theoretically less subject to error than those methods employ-ing an indicating instrument,provided,however,that the potentiometer voltage is accurately known.The error in R s is to some extent dependent on the amplifier sensitivity.For mea-surement of a given current,the higher the amplifier sensitivity,the greater likelihood that lower valued,highly precise wire-wound standard resistors can be used.Such amplifiers can be obtained.Standard resistances of 100G V known to 62%,are available.If 10-mV input to the amplifier or electrometer gives full-scale deflection with an error not greater than 2%of full scale,with 500V applied,a resistance of 5000T V can be measured with a maximum error of 6%when the voltmeter reads full scale,and 10%when it reads 1⁄3scale.7.5.2.3Comparison-Galvanometer —The maximum per-centage error in the computed resistance or conductance is given by the sum of the percentage errors in R s ,the galvanom-eter deflections or amplifier readings,and the assumption that the current sensitivities are independent of the deflections.The latter assumption is correct to well within 62%over the useful range (above 1⁄10full-scale deflection)of a good,modern galvanometer (probably 1⁄3scale deflection for a dc current amplifier).The error in R s depends on the type of resistor used,but resistances of 1M V with a limit of error as low as 0.1%are available.With a galvanometer or d-c current amplifier having a sensitivity of 10nA for full-scale deflection,500V applied to a resistance of 5T V will produce a 1%deflection.At this voltage,with the preceding noted standard resistor,and with F s =105,d s would be about half of full-scale deflection,with a readability error not more than 61%.If d x is approxi-mately 1⁄4of full-scale deflection,the readability error would not exceed 64%,and a resistance of the order of 200G V could be measured with a maximum error of 651⁄2%.7.5.2.4Voltage Rate-of-Change —The accuracy of the mea-surement is directly proportional to the accuracy of the measurement of applied voltage and time rate of change of the electrometer reading.The length of time that the electrometer switch is open and the scale used should be such that the time can be measured accurately and a full-scale reading obtained.Under these conditions,the accuracy will be comparable with that of the other methods of measuring current.7.5.2.5Comparison Bridge —When the detector has ad-equate sensitivity,the maximum percentage error in the com-puter resistance is the sum of the percentage errors in the arms,A,B,and N .With a detector sensitivity of 1mV/scale division,500V applied to the bridge,and R N =1G V ,a resistance of 1000T V will produce a detector deflection of one scale division.Assuming negligible errors in R A and R B ,with R N =1G V known to within 62%and with the bridge balanced to one detector-scale division,a resistance of 100T V can be mea-sured with a maximum error of 66%.FIG.9Connections to Guarded Electrode for Volume and Surface Resistivity Measurements (Volume Resistance hook-upshown)FIG.10Connections to Unguarded Electrodes for Volume and Surface Resistivity Measurements (Surface Resistance Hook-UpShown)--`,,```,,,,````-`-`,,`,,`,`,,`---。

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