(1)ASTM D2216-98 试验室测定土和岩石含水量标准试验方法

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岩石力学实验-煤和岩石含水率测定实验

岩石力学实验-煤和岩石含水率测定实验

实验二、岩石含水率的测定
一、实验目的
煤或岩石含水率是指煤或岩石在天然状态下所含水分的质量与其烘干后的质量之比。

通过本实验,要了解煤(岩石)含水率测试程序及测试仪器设备,掌握煤(岩石)含水率测试过程及计算方法。

二、实验仪器及工具
1、岩石试件
2、烘箱
3、干燥器
4、天平
三、实验原理
实验的含水率应按照下式计算:
−1)×100%
ω=(M1
M2
式中
ω—煤或岩石的自然吸水率;
M1—保持天然水分的试件质量,g;
M2—烘干的试件质量,g。

四、实验步骤
1、取保持天然含水状态,尺寸大于组成岩石最大矿物颗粒直径的10倍,且质量不少于50g的三个试件,立即称重得M1;
2、将不含结晶水的试样放在105~110o C的烘箱内烘干24h,放在干燥器内冷却至室温,称重得M2;
3、将含结晶水的试样放在55~65o C的烘箱内烘干24h,放在干燥器内冷却至室温,称重得M2。

五、实验现象及数据记录
六、实验结果及数据分析
将实验数据带入上述公式得:
−1)×100%
ω=(M1
M2
=0.138%
即所测试件的含水率为0.138%。

七、心得体会
通过本次实验,我不仅学会了如何测定煤和岩石的含水率,也对电热烘箱的使用方法有所了解。

做实验要时刻牢记实验步骤和原理,这样才能降低实验的失误率。

时刻保持专注也是保证实验成功的一个重要因素。

这个实验让我受益匪浅。

击实试验(轻型)

击实试验(轻型)

设计编号:D698-00a击实试验(轻型)标准参测试方法本规范是在制定设计编号:D698下出版的,紧随指定设计编号:的数字表明本规范最早被采用的年份,或者最后修正的年份,插入的数字表示最后修正的年份。

上标的字母表明从最近一次修正或评审以来的在编辑上的变化。

1. 范围1.1 该方法适用于确定土的含水量和干容重之间关系(压缩曲线)的实验。

这些试验将土置于直径为4-6 in.(101.6-152.4 mm)的磨具中,并用5.5 lbf(24.4N)的夯锤从12 in.(305mm)高度落下形成12400ft-lbf/ft3(600kN-m/m3)的作用力。

注1-试验设备和过程都比R. R. Proctor(Engineering New Record-1933.9.7)所提出的小,但是在以下方面是例外的:R. R. Proctor提出的夯锤打击方式采用固定长度12 in.(305 mm)的敲击而不是自由落体,因此,由此而产生不同的压缩作用力取决于实验者,但是其作用力范围在15000-25000 ft-lbf/ft3(700-1200kN-m/m3)之间。

标准的作用力测试(见3.2.2)有时是指Proctor实验。

注2-天然产生的粗粒或者细粒土,天然土的合成物或混合物,天然土和人工图的混合物,以及由粘土,砾石和压碎的岩石组成的团聚体都可以被认为是土以及土的团聚体混合物。

1.2 测试方法适用于含有小于等于30%的颗粒不能通过3/4 in.(19.0 mm)筛子的土。

注3-关于含有小于等于30%的颗粒不能通过3/4 in.(19.0 mm)的筛子的土的容重和含水量的关系受到可通过3/4 in.(19.0mm)的筛子的颗粒的容重和含水量的影响,见实践D4718。

1.3 本标准提供了3个可供选择的实验方法。

对于待测的材料,应该按照说明选择实验方法,如果说明没有指定实验方法,则应该根据材料的颗粒级配选择实验方法。

土壤含水量测定方法小结

土壤含水量测定方法小结

土壤含水量测定方法小结1.干湿法称重法干湿法称重法是一种比较常用的测定土壤含水量的方法,它是通过比较土壤的湿重和干重来计算土壤含水量的。

具体步骤如下:(1)从待测土壤样品中取一定质量的土壤样本,记录其湿重并置于105℃下干燥至恒重。

(2)计算土壤的含水量,公式为:土壤含水量(%)=(湿重-干重)/湿重×100%。

这种方法简单易行,不需要复杂的仪器设备,但存在一定的误差。

2.速效土壤含水量的测定速效土壤含水量是指土壤中表层土壤(一般为0-30厘米)中的土壤含水量,它对农作物的生长和灌溉决策具有重要意义。

常见的速效土壤含水量测定方法包括压实法、蓄水法和电导率法等。

(1)压实法:将土壤样品放入标准容器中,进行标准重力处理,然后测定容器中土壤和水的质量,从而计算土壤容重。

(2)蓄水法:将土壤样品放入带孔的土壤柱中,通过灌溉一定量的水,测定出流水的数量,从而计算土壤含水量。

(3)电导率法:利用土壤含水量与土壤电导率之间的关系来测定土壤含水量。

通过测定土壤电导率,可以反推出土壤含水量。

3.艾弗姆法艾弗姆法是一种常用的测定土壤含水量的方法,它是利用土壤中的吸力作为土壤含水量的指示器,通过测定土壤中的吸力来计算土壤含水量。

这种方法需要使用土壤水分特性曲线,还需要相关的仪器和设备进行测定。

4.放射性测定法放射性测定法是一种利用放射性同位素测定土壤含水量的方法。

通过测定土壤中放射性同位素的衰减和浓度变化,可以计算出土壤含水量。

这种方法需要专门的设备和保护措施,操作较为复杂。

5.土壤水分传感器法土壤水分传感器法是一种利用土壤水分传感器测定土壤含水量的方法。

这种方法可以实时、连续地监测土壤水分变化,在农田灌溉和土壤水分管理中具有广泛的应用。

根据传感器的不同原理,包括电容法、电阻法、微波法等多种类型。

总结起来,测定土壤含水量的方法有干湿法称重法、速效土壤含水量的测定方法、艾弗姆法、放射性测定法以及土壤水分传感器法等。

不同规范土的含水率试验方法比较与分析

不同规范土的含水率试验方法比较与分析

不同规范土的含水率试验方法比较与分析作者:王协群周琪周申培黄珍来源:《中国教育技术装备》2020年第20期摘要土的含水率試验是一项最基本的土的物理性质试验,国内外试验方法较多。

对国外应用较多的美国材料与试验协会(ASTM)标准和我国国标(GB)及两种行业标准(JTG和DL)中关于含水率的试验方法进行对比分析,找出国内外规范以及国内不同行业规范之间的异同,使学生了解不同规范间的差别,并为土木工程从业人员结合实际工程情况选择合适的试验方法提供参考。

关键词土的含水率试验;试验仪器;烘干法;酒精燃烧法;比重法;炒干法;微波炉法中图分类号:G642 文献标识码:B文章编号:1671-489X(2020)20-0117-03Abstract Soil moisture content test is a basic geotechnical test, which has various test methods at home and abroad. The moisture content test methods in the standard of American Society for Testing and Materials (ASTM) which is widely used abroad and the national standard (GB) and two industry standards (JTG and DL) in China areselected to introduce and compare. To find out the similarities anddifferences between domestic and foreign codes and codes of diffe-rent industries, so that university students can understand the diffe-rences between different codes, and provide references for civil engi-neering practitioners to choose appropriate test methods based on actual engineering conditions.Key words soil moisture content testt; drying method; alcohol bur-ning method; specific gravity method; fried dry method; microwave oven method1 前言土的含水率是指土中水的质量与土固体颗粒质量的比值,以百分数表示[1]。

土的含水量试验

土的含水量试验

土的含水量试验土的含水量试验(烘干法、酒精燃烧法)土的含水量试验(烘干法、酒精燃烧法)烘干法一、定义土的含水量是在105-110℃下烘至恒量时所失去的水分质量和达恒量后干土质量的比值,以百分数表示,本法是测定含水量的标准方法。

二、适用范围粘质土、粉质土、砂类土和有机质土类。

三、主要仪器设备烘箱:可采用电热烘箱或温度能保持105-110℃的其他能源烘箱,也可用红外线烘箱天平:感量0.01g。

称量盒(定期调整为恒质量)四、计算公式含水量=(湿土质量-干土质量)/干土质量×100%注:计算至0.1%。

五、允许差值本试验须进行二次平行测定,取其平均算术平均值,允许平行差值应符合如下规定含水量(%)允许平行差值(%)5以下0.340以下≤140以上≤2酒精燃烧法一、适用范围本法适用于快速简易测定细粒土(含有机质的除外)的含水量。

二、主要仪器设备称量盒(定期调整为恒质量)。

天平:感量0.01g。

酒精:纯度95%。

三、其余同"烘干法"土的颗粒分析试验(筛分法、比重计法)筛分法一、适用范围适用于分析粒径大于0.074mm的土。

二、主要仪器设备标准筛:粗筛(圆孔):孔径为60mm、40mm、20mm、10mm、5mm、2mm;细筛:孔径为2mm、0.5mm、0.25mm、0.074mm。

天平:称量5000g,感量5g;称量1000g,感量1g;称量200g,感量0.2g。

三、试样从风干、松散的土样中,用四分法按照下列规定取出具有代表性的试样:小于2mm颗粒的土100-300g。

最大粒径小于10mm的土300-900g。

最大粒径小于20mm的土1000-2000g。

最大粒径小于40mm的土2000-4000g。

最大粒径大于40mm的土4000g以上。

四、计算公式按下式计算小于某粒径颗粒质量百分数:X=(A/B)×100式中:X-小于某粒径颗粒的质量百分数,%;A-小于某粒径的颗粒质量,g;B-试样的总质量,g。

岩石的含水率试验方法

岩石的含水率试验方法

岩石的含水率试验方法
1. 依据标准:《公路工程岩石试验规程》JTG E41-2005 (T0202-2005 );
2. 试验目的及适用范围:
2.1含水率试验用于测定岩石在天然状态下的含水率。

岩石的含水率可
以间接地反映岩石中空隙的多少、岩石的致密程度等特性。

2.2本试验采用烘干法。

对于不含结晶水矿物的岩石烘干温度为105°C~11C°C;对于含结晶水矿物的岩石温度宜控制在600C~± 50C下进行测定。

3. 试验环境:进入试验室内先检查温湿度仪,并在记录中注明试验时室内的温湿度。

4. 试验准备:
4.1仪器设备
4.2试样制备
4.2.1保持天然含水率的试件应在现场采取,严禁用爆破法或湿钻法。

试件在采
取、运输、储存和制备过程中,含水率变化不应超过过1%。

土的含水量试验(烘干法)检测_secret

土的含水量试验(烘干法)检测_secret

土的含水量试验(烘干法)检测1 定义和适用范围1.1 目的:土的含水量是在105~110℃下烘至恒量时所失去的水分质量和达恒量后干土质量的比值,以百分数表示,本法是测定含水量的标准方法。

1.2 本试验方法适用于粘质土、粉质土、砂类土和有机质土类。

2 仪器设备2.1 烘箱:可采用电热烘箱或温度能保持105~110℃的其它能源烘箱,也可用红外线烘箱。

2.2 天平:感量0.01g。

2.3 其它:干燥器、称量盒(为简化计算手续,可将盒质量定期(3~6个月)调整为恒质量值)等。

3 试验步聚3.1 取具有代表性试样,细粒上15~30g,砂类上、有机质土为50g,放入称量盒内,立即盖好盒盖,称质量。

称量时,可在天平一端放上与该称量盒等质量的法码,移动天平游码,平衡后称量结果即为湿土质量。

3.2 揭开盒盖,将试样和盒放入烘箱内,在温度105~110℃恒温下烘干。

烘干时间对细粒上不少于8h,对砂类上不得少于6h。

对含有机质超过5%的土,应将温度控制在65~70℃的恒温下烘干。

3.3 将烘干后的试样和盒取出,放入干燥器内冷却(一般只需0.5h ~1h 即可)。

冷却后盖好盒盖,称质量,准确至0.01g 。

4 计算4.1 按下式计算含水量:100m m -m w ss ⨯= 式中:w ——含水量,%;m ——湿土质量,g ;m s ——干土质量,g ;计算至0.1%。

5 精密度和允许差本试验须进行二次平行测定,取其算术平均值作为测定结果。

允许平行差值如表3.4-1。

含水量测定的允许平行差值 表3.4-16 出报告6.1 报告中应写出土的鉴别分类和代号。

6.2 土的含水量。

7 注意事项7.1 测试前后应仔细检查仪器的安装联结状况,确保仪器处于正常工作状态。

7.2 试验结果若超出允许差范围,则应重新取样,进行试验。

7.3 测试过程中,若发生停电等意外情况,应待有电或意外情况消除后,再进行试验。

7.4 试验过程中,若仪器、设备发生故障或损坏,应待仪器、备修复后,再进行试验。

土工试验含水率测定方法

土工试验含水率测定方法

土工试验含水率测定方法
《土工试验含水率测定方法》
嘿,大家知道不,在土工试验里,含水率的测定那可是相当重要的事儿呢!
我记得有一次在实验室里,我们就进行了一次含水率测定的实验。

那场面,可有意思啦!我们先把从工地取回来的土样小心翼翼地放在托盘上,就好像对待宝贝一样。

然后呢,把它放进烘箱里,那烘箱就像是一个大烤炉,要把土样里的水分都给烤出来。

在等待的过程中,我们一群人就在旁边眼巴巴地看着烘箱,心里都在想着:“哎呀,这土样的水分啥时候才能被烤干呀。

”时间一分一秒地过去,感觉过得好慢好慢哦。

终于,烘箱的时间到啦,我们迫不及待地把土样拿出来。

哇,那土样变得干巴巴的,和之前完全不一样了。

接着,我们就得称一称这干土的重量啦。

拿着天平,那感觉就像是在称金子一样仔细。

称完了干土重,再和之前取土样时的重量一对比,就能算出含水率啦。

你可别小看这个含水率的测定,它能告诉我们很多关于土的性质呢,对工程建设可是有着很大的影响哟!
这就是我亲身经历的土工试验含水率测定的过程,是不是还挺有趣的呀。

每次想到这个实验,我都觉得特别有意思,也更加深刻地体会到了含水率测定的重要性呢!哈哈!。

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D6026Guide for Using Significant Digits in Calculating and Reporting Geotechnical Test Data5E145Specification for Gravity-Convection And Forced-Ventilation Ovens63.Terminology3.1Refer to Terminology D653for standard definitions of terms.3.2Definitions of Terms Specific to This Standard:3.2.1water content(of a material)—the ratio expressed as a percent of the mass of“pore”or“free”water in a given mass of material to the mass of the solid material.A standard temperature of110°65°C is used to determine these masses.4.Summary of Test Method4.1A test specimen is dried in an oven at a temperature of 110°65°C to a constant mass.The loss of mass due to drying is considered to be water.The water content is calculated using the mass of water and the mass of the dry specimen.5.Significance and Use5.1For many materials,the water content is one of the most significant index properties used in establishing a correlation between soil behavior and its index properties.5.2The water content of a material is used in expressing the phase relationships of air,water,and solids in a given volume of material.5.3Infine-grained(cohesive)soils,the consistency of a given soil type depends on its water content.The water content of a soil,along with its liquid and plastic limits as determined by Test Method D4318,is used to express its relative consis-tency or liquidity index.6.Apparatus6.1Drying Oven,thermostatically-controlled,preferably of the forced-draft type,meeting the requirements of Specifica-tion E145and capable of maintaining a uniform temperature of11065°C throughout the drying chamber.6.2Balances—All balances must meet the requirements of Specification D4753and this section.A Class GP1balance of 0.01g readability is required for specimens having a mass of up to200g(excluding mass of specimen container)and a Class GP2balance of0.1g readability is required for specimens having a mass over200g.However,the balance used may be controlled by the number of significant digits needed(see8.2.1 and12.1.2).6.3Specimen Containers—Suitable containers made of ma-terial resistant to corrosion and change in mass upon repeated heating,cooling,exposure to materials of varying pH,and cleaning.Unless a dessicator is used,containers with close-fitting lids shall be used for testing specimens having a mass of less than about200g;while for specimens having a mass greater than about200g,containers without lids may be used (see Note7).One container is needed for each water content determination.N OTE2—The purpose of close-fitting lids is to prevent loss of moisture from specimens before initial mass determination and to prevent absorp-tion of moisture from the atmosphere following drying and beforefinal mass determination.6.4Desiccator—A desiccator cabinet or large desiccator jar of suitable size containing silica gel or anhydrous calcium sulfate.It is preferable to use a desiccant which changes color to indicate it needs reconstitution.See10.5.N OTE3—Anhydrous calcium sulfate is sold under the trade name Drierite.6.5Container Handling Apparatus,gloves,tongs,or suit-able holder for moving and handling hot containers after drying.6.6Miscellaneous,knives,spatulas,scoops,quartering cloth,sample splitters,etc,as required.7.Samples7.1Samples shall be preserved and transported in accor-dance with Practice4220Groups B,C,or D soils.Keep the samples that are stored prior to testing in noncorrodible airtight containers at a temperature between approximately3and30°C and in an area that prevents direct contact with sunlight. Disturbed samples in jars or other containers shall be stored in such a way as to prevent or minimize moisture condensation on the insides of the containers.7.2The water content determination should be done as soon as practicable after sampling,especially if potentially corrod-ible containers(such as thin-walled steel tubes,paint cans,etc.) or plastic sample bags are used.8.Test Specimen8.1For water contents being determined in conjunction with another ASTM method,the specimen mass requirement stated in that method shall be used if one is provided.If no minimum specimen mass is provided in that method then the values given below shall apply.See Howard7for background data for the values listed.8.2The minimum mass of moist material selected to be representative of the total sample shall be in accordance with the following:Maximum particlesize(100%passing)Standard SieveSizeRecommendedminimum mass ofmoist test spec-imen for watercontent reportedto60.1%Recommendedminimum mass ofmoist test spec-imen for watercontent reportedto61%2mm or less No.1020g20g A4.75mm No.4100g20g A9.5mm3⁄8-in.500g50g19.0mm3⁄4-in. 2.5kg250g37.5mm11⁄2in.10kg1kg75.0mm3-in.50kg5kgA To be representative not less than20g shall be used.8.2.1The minimum mass used may have to be increased to obtain the needed significant digits for the mass of water when reporting water contents to the nearest0.1%or as indicated in 12.1.2.5Annual Book of ASTM Standards,V ol04.09. 6Annual Book of ASTM Standards,V ol14.02.7Howard,A.K.,“Minimum Test Specimen Mass for Moisture Content Deter-mination”,Geotechnical Testing Journal,A.S.T.M.,V ol.12,No.1,March1989,pp.39-44.8.3Using a test specimen smaller than the minimum indi-cated in8.2requires discretion,though it may be adequate for the purposes of the test.Any specimen used not meeting these requirements shall be noted on the test data forms or test data sheets.8.4When working with a small(less than200g)specimen containing a relatively large gravel particle,it is appropriate not to include this particle in the test specimen.However,any discarded material shall be described and noted on the test data forms or test data sheets.8.5For those samples consisting entirely of intact rock,the minimum specimen mass shall be500g.Representative portions of the sample may be broken into smaller particles, depending on the sample’s size,the container and balance being used and to facilitate drying to constant mass,see10.4. Specimen sizes as small as200g may be tested if water contents of only two significant digits are acceptable.9.Test Specimen Selection9.1When the test specimen is a portion of a larger amount of material,the specimen must be selected to be representative of the water condition of the entire amount of material.The manner in which the test specimen is selected depends on the purpose and application of the test,type of material being tested,the water condition,and the type of sample(from another test,bag,block,and the likes.)9.2For disturbed samples such as trimmings,bag samples, and the like,obtain the test specimen by one of the following methods(listed in order of preference):9.2.1If the material is such that it can be manipulated and handled without significant moisture loss and segregation,the material should be mixed thoroughly and then select a repre-sentative portion using a scoop of a size that no more than a few scoopfuls are required to obtain the proper size of specimen defined in8.2.9.2.2If the material is such that it cannot be thoroughly mixed or mixed and sampled by a scoop,form a stockpile of the material,mixing as much as possible.Take at leastfive portions of material at random locations using a sampling tube, shovel,scoop,trowel,or similar device appropriate to the maximum particle size present in the bine all the portions for the test specimen.9.2.3If the material or conditions are such that a stockpile cannot be formed,take as many portions of the material as practical,using random locations that will best represent the moisture bine all the portions for the test specimen.9.3Intact samples such as block,tube,split barrel,and the like,obtain the test specimen by one of the following methods depending on the purpose and potential use of the sample. 9.3.1Using a knife,wire saw,or other sharp cutting device, trim the outside portion of the sample a sufficient distance to see if the material is layered and to remove material that appears more dry or more wet than the main portion of the sample.If the existence of layering is questionable,slice the sample in half.If the material is layered,see9.3.3.9.3.2If the material is not layered,obtain the specimen meeting the mass requirements in8.2by:(1)taking all or one-half of the interval being tested;(2)trimming a represen-tative slice from the interval being tested;or(3)trimming the exposed surface of one-half or from the interval being tested. N OTE4—Migration of moisture in some cohesionless soils may require that the full section be sampled.9.3.3If a layered material(or more than one material type is encountered),select an average specimen,or individual speci-mens,or both.Specimens must be properly identified as to location,or what they represent,and appropriate remarks entered on the test data forms or test data sheets.10.Procedure10.1Determine and record the mass of the clean and dry specimen container(and its lid,if used).10.2Select representative test specimens in accordance with Section9.10.3Place the moist test specimen in the container and,if used,set the lid securely in position.Determine the mass of the container and moist material using a balance(see6.2)selected on the basis of the specimen mass.Record this value.N OTE5—To prevent mixing of specimens and yielding of incorrect results,all containers,and lids if used,should be numbered and the container numbers shall be recorded on the laboratory data sheets.The lid numbers should match the container numbers to eliminate confusion.N OTE6—To assist in the oven-drying of large test specimens,they should be placed in containers having a large surface area(such as pans) and the material broken up into smaller aggregations.10.4Remove the lid(if used)and place the container with moist material in the drying oven.Dry the material to a constant mass.Maintain the drying oven at11065°C unless otherwise specified(see 1.4).The time required to obtain constant mass will vary depending on the type of material,size of specimen,oven type and capacity,and other factors.The influence of these factors generally can be established by good judgment,and experience with the materials being tested and the apparatus being used.N OTE7—In most cases,drying a test specimen overnight(about12to 16h)is sufficient.In cases where there is doubt concerning the adequacy of drying,drying should be continued until the change in mass after two successive periods(greater than1h)of drying is an insignificant amount (less than about0.1%).Specimens of sand may often be dried to constant mass in a period of about4h,when a forced-draft oven is used.N OTE8—Since some dry materials may absorb moisture from moist specimens,dried specimens should be removed before placing moist specimens in the same oven.However,this would not be applicable if the previously dried specimens will remain in the drying oven for an additional time period of about16h.10.5After the material has dried to constant mass remove the container from the oven(and replace the lid if used).Allow the material and container to cool to room temperature or until the container can be handled comfortably with bare hands and the operation of the balance will not be affected by convection currents and/or its being heated.Determine the mass of the container and oven-dried material using the same type/capacity balance used in10.3.Record this value.Tightfitting lids shall be used if it appears that the specimen is absorbing moisture from the air prior to determination of its dry mass.N OTE9—Cooling in a desiccator is acceptable in place of tightfitting lids since it greatly reduces absorption of moisture from the atmosphere during cooling especially for containers without tightfittinglids.11.Calculation11.1Calculate the water content of the material as follows:w5@~M cws2M cs!/~M cs2M c!#31005M wM s3100(1)where:w5water content,%,M cws5mass of container and wet specimen,g,M cs5mass of container and oven dry specimen,g,M c5mass of container,g,M w5mass of water(M w5M cws−M cds),g,andM s5mass of solid particles(M s5M cds−M c),g. 12.Report12.1Test data forms or test data sheets shall include the following:12.1.1Identification of the sample(material)being tested, such as boring number,sample number,test number,container number etc.12.1.2Water content of the specimen to the nearest1%or 0.1%,as appropriate based on the minimum sample used.If this method is used in concert with another method,the water content of the specimen should be reported to the value required by the test method for which the water content is being determined.Refer to Guide D6026for guidance con-cerning significant digits,especially if the value obtained from this test method is to be used to calculate other relationships such as unit weight or density.For instance,if it is desired to express dry unit weight to the nearest0.1lbf/f3(0.02kN/m3),it may be necessary to use a balance with a greater readability or use a larger specimen mass to obtain the required significant digits the mass of water so that the water content can be determined to the required significant digits.Also,the signifi-cant digits in Guide D6026may need to be increased when calculating phase relationships requiring four significant digits.12.1.3Indicate if test specimen had a mass less than the minimum indicated in8.2.12.1.4Indicate if test specimen contained more than one material type(layered,etc.).12.1.5Indicate the temperature of drying if different from 11065°C.12.1.6Indicate if any material(size and amount)was excluded from the test specimen.12.2When reporting water content in tables,figures,etc., any data not meeting the requirements of this test method shall be noted,such as not meeting the mass,balance,or temperature requirements or a portion of the material is excluded from the test specimen.13.Precision and Bias13.1Statement on Bias—There is no accepted reference value for this test method;therefore,bias cannot be deter-mined.13.2Statements on Precision:13.2.1Single-Operator Precision(Repeatability)—The single-operator coefficient of variation has been found to be2.7 percent.Therefore,results of two properly conducted tests by the same operator with the same equipment should not be considered suspect unless they differ by more than7.8percent of their mean.813.2.2Multilaboratory Precision(Reproducibility)9—The multilaboratory coefficient of variation has been found to be 5.0percent.Therefore,results of two properly conducted tests by different operators using different equipment should not be considered suspect unless they differ by more than14.0percent of their mean.14.Keywords14.1consistency;index property;laboratory;moisture analysis;moisture content;soil aggregate;water contentSUMMARY OF CHANGESCommittee D-18has identified the location of selected changes to this standard since the last issue. (D2216-92)that may impact the use of this standard.(1)Title was changed to emphasize that mass is the basis for the standard.(2)Section1.1was revised to clarify“similar materials”.(3)New1.2was added to explain a limitation in scope.The other sections were renumbered as appropriate.(4)An information reference was included in1.5.(5)An information reference was included in1.6(6)A new ASTM referenced document was included in2.1.(7)New Footnotes2,3,and5were added and identified. Other footnotes were renumbered where necessary for sequen-tial identification.(8)Information concerning balances was added in6.2(9)Section6.3was revised to clarify the use of close-fitting lids,and a reference to Note8was added.(10)In6.4,“anhydrous calcium phosphate”was changed to “anyhydrous calcium sulfate”to correct an error and to agree with Note3.(11)A typo in8.1was corrected from“before”to“below”anda footnoted reference was added for information.(12)A portion of8.2was deleted for clarity.(13)A new8.2.1was added to clarify minimum mass require-ments.(14)Sections8.3,8.4,9.3.3,and12.1were changed to substitute“test data form/sheet”for“report”.(15)Footnote seven was identified.(16)Section9.2.1was revised to improve clarity and intent.(17)The word“possible”was changed to“practical”in9.2.3.8These numbers represent the(1s)and(d2s)limits as described in Practice C 670.9These numbers represent the(1s%)and(d2s%)limits as described in Practice C670.(18)Section 9.3.1and 9.3.2were revised to improve clarityand for practicality.(19)A reference to Guide D 6026was added in 12.1.2.(20)Footnotes 8and 9were added to 13.2.1and 13.2.2,respectively.These were inadvertently omitted from the 1992version.These explanations provide clarity and information to the user.(21)A Summary of Changes was added to reflect D-18’s policy.The American Society for Testing and Materials takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this ers of this standard are expressly advised that determination of the validity of any such patent rights,and the risk of infringement of such rights,are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years and if not revised,either reapproved or withdrawn.Your comments are invited either for revision of this standard or for additional standards and should be addressed to ASTM Headquarters.Your comments will receive careful consideration at a meeting of the responsible technical committee,which you may attend.If you feel that your comments have not received a fair hearing you should make your views known to the ASTM Committee on Standards,100Barr Harbor Drive,West Conshohocken,PA19428.。

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