Astm D409 D409M - 2011 - 208417808126
Astm D409 D409M - 2011 - 208417808126
Astm D409 D409M - 2011 - 208417808126
INTRODUCTION
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
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2. Referenced Documents NOTE 1—A single balance meeting the specifications of 4.3 and 4.4 is
permitted.
2.1 ASTM Standards:3
D2013 Practice for Preparing Coal Samples for Analysis 4.5 Calibration Weights—These calibration weights shall
be used periodically to monitor the response of each balance
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D2234/D2234M Practice for Collection of a Gross Sample
of Coal over the working range.
D3302 Test Method for Total Moisture in Coal 4.6 Sample Divider— An enclosed riffle divider with feed
D4749 Test Method for Performing the Sieve Analysis of chute as described in Practice D2013 or a rotary sample
Coal and Designating Coal Size divider, which has been proven to be free of significant bias,
D6708 Practice for Statistical Assessment and Improvement may be used.
of Expected Agreement Between Two Test Methods that 4.7 Standard Sieves—A working set of circular, standard
Purport to Measure the Same Property of a Material testing sieves, which are 203 mm [8 in.] in diameter and
D6883 Practice for Manual Sampling of Stationary Coal conform to Specification E11, are required in the following
from Railroad Cars, Barges, Trucks, or Stockpiles sizes, together with cover and catch pan (receiver):
D7430 Practice for Mechanical Sampling of Coal
E11 Specification for Woven Wire Test Sieve Cloth and Test TABLE 1 Standard Sieves for HGI Testing
Sieves E11 Specification U.S.A. Standard Sieve Series Designation
16.0 mm 5⁄8 in.
pulverizing process, which can impact a wide variety of 4.7.1 These working sieves must be periodically inspected
processes, including combustion, coke-making, liquefaction, for wear or damage. Any excessively worn or damaged sieves
and gasification. (for example, sieves with holes, tears, cracks; etc.) must be
replaced immediately, and the HGI calibration procedure must
4. Apparatus be repeated after the damaged sieves are replaced (see Annex
4.1 Air-Drying Oven [for air-drying the 1000 g, 4.75 mm A5). Since the HGI depends upon the sieve analysis and since
(No. 4) sample]—A device for passing slightly heated air over the 75-µm (No. 200) sieve is fragile, it is recommended that at
the sample. The oven shall be capable of maintaining a least one set of working sieves be obtained, identified, and used
temperature of 10 to 15 °C [18 to 27 °F] above room tempera- exclusively for HGI determinations and that only this exclusive
ture with a maximum oven temperature of 40 °C [104 °F] set of sieves be used for determining HGI.
unless ambient temperature is above 40 °C, in which case 4.7.1.1 Excessive wear may be indicated by poor repeatabil-
ambient temperature shall be used. In the case of easily ity or by failure of quality control checks (A5.4.1.1) to agree
oxidized coals, the temperature shall not be over 10 °C [18 °F] reasonably with the initial calibration data.
above room temperature unless ambient temperature is above 4.7.2 Normal wear on sieves is compensated by the use of
37 °C [100 °F] in which case ambient temperature shall be primary HGI standard reference samples (HGI RMs) and
used. Air changes shall be at the rate of 1 to 4 air volumes of proper calibration of equipment; excessive wear (such as holes
oven capacity per minute. or tears in the sieve cloth, and so forth) is not compensated by
4.2 Drying Pans [for air-drying the 1000 g, 4.75 mm (No. 4) HGI RMs. Because excessive wear is unacceptable, inspect
sample]—Drying pans of sufficient size so that the sample may sieves carefully before each test to ensure the absence of
be spread to a depth of not more than 25 mm [1.0 in.] with excessive wear. For the 75- and 600-µm (No. 200 and 30)
sides not more than 38 mm [1.5 in.] high. The pans shall be sieves, use only a soft-bristled brush (such as short-bristled
nonreactive with coal and unaffected by the method of air camel hair) for brushing and cleaning.
drying selected. 4.7.2.1 It is good practice to keep a separate primary 75-µm
4.3 Balance [for weighing the 1000-g sample before and (No. 200) check sieve to be used only to check the 75-µm (No.
after air-drying and the sieve fractions formed during stage- 200) working sieves described in 4.7.1 whenever the working
crushing]—With a sensitivity of at least 0.5 g in 1000 g and sieve becomes suspect. This check is done by running a
comparative HGI test between the two 75-µm (No. 200) sieves.
Use of the working sieve for HGIs should be discontinued if
3
For referenced ASTM standards, visit the ASTM website, www.astm.org, or HGI difference between the sieves is greater than 1 HGI unit.
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
Standards volume information, refer to the standard’s Document Summary page on 4.8 Plate Mill Crusher—A laboratory plate mill capable of
the ASTM website. reducing 4.75-mm (No. 4) sieve size coal particles with the
sieves during hand sieving by imparting a horizontal oscilla- other international or national standard) except that the sample
tory motion of approximately 28-mm [1.1-in.] amplitude at a topsize shall not be reduced beyond the 4.75-mm (No. 4) sieve
rate of approximately 300 oscillations or cycles per minute and the sample shall have a mass of at least 1000 g.
(cpm). Simultaneously, the top of the oscillating assembly is 5.2 If the topsize of the final sample product produced from
struck at a rate of approximately 150 blows per minute by a mechanical sampling system is smaller than 4.75mm (No. 4),
mass of 1.9 kg [4.2 lb] moving through a vertical distance of the sample does not meet the requirements of this test
approximately 28 mm [1.1 in.] under the influence of gravity. procedure.
4.9.1 Whenever a mechanical sieving machine other than
the reference machine described above is used, the method 6. Preparation of Test Samples
may be shown to be equivalent by one of two methods (1) side 6.1 Prepare a 1.18 3 0.60 mm (No. 16 3 30) test sample
x side equivalency testing of the alternative machine vs. the for establishing the HGI of HGI RMs (Annex A4 ), for
reference machine (with both calibration and test samples that calibration (Annex A5), or for routine determination of HGI.
cover the working range), using the equivalency testing statis- 6.2 When necessary, divide the quantity of 4.75-mm (No. 4)
tical technique of D6708 or (2) acceptable performance in an sieve size coal to not less than 1000-g lots using an enclosed
appropriate proficiency test program that covers the working riffle or rotary sample divider, and air dry each sample in
range. conformance with Test Method D3302. To calculate the
4.10 Grindability Machine—The Hardgrove Grindability % Yield (8.3), record the mass of the air-dried sample (m1).
Machine such as is shown in Fig. 1 is required for this test. 6.3 Sieve the entire amount (1000 g) of air-dried 4.75-mm
Essential tolerances and specifications are shown in Fig. 2. The (No. 4) sieve size sample in lots of no greater than 250 g for 2
grindability machine includes a stationary grinding bowl of min 6 10 s in the mechanical sieving machine. Use a set of
polished cast iron, with a circular horizontal track that holds nested sieves consisting of a 1.18-mm (No. 16) sieve on top of
eight polished steel balls, each 25.40 6 0.13 mm [1.000 6 a 0.60-mm (No. 30) sieve. Weigh and record the mass of each
0.005 in.] in diameter. The balls are driven by an upper sieve size.
grinding ring which is rotated at 20 6 1 r/min by means of the 6.3.1 Include a 4.75-mm (No. 4) and a 2.36-mm (No. 8)
upper spindle and which, in turn, is driven by an electric motor sieve in this nest of sieves to ease separation, determine and
through reduction gears or, in newer models, belts. Weights are record the “natural” particle size distribution, and to verify that
added to the driving spindle so that the total vertical force on the topsize of the sample is appropriate for this test. Sieving
the balls as a result of the weights, shaft, top grinding ring, and more than 250 g at a time on the 200-mm [8-in.] diameter sieve
gear is equal to 29.0 6 0.2 kg [64 6 0.5 lb]. The machine is may not allow each particle to “see” the sieve surface and have
equipped with a counter and automatic device, which can be an opportunity to pass or to be retained by the sieve.
properly adjusted for stopping the machine after 60 6 0.25 6.4 Combine and stage crush all of the sieve fractions
revolutions. greater than the 1.18-mm (No. 16) sieve with the crusher
adjusted so that only the largest particles are crushed. Sieve the
crushed material in portions of no greater than 250 g for 2 min
4
D05.07 Minutes, J. Gardner, Georgia Power and G. Linton, October 1990. 6 10 s in the mechanical sieving machine. Return the oversize
to the crusher, after setting the crusher so that only the largest 6.6.1 Determining the mass of each sieve fraction after each
particles are crushed. Continue the stage crushing and sieving stage-crushing step will allow the rate of reduction to be
procedure until all the material passes the 1.18-mm sieve. calculated and evaluated as a contributor to achieving adequate
Retain the 1.18 3 0.60 mm (No. 16 3 30) material. After all % Yield.
stage-crushing is completed, to calculate the % Yield (8.3),
record the mass of the 1.18 3 0.60 mm (No. 16 3 30) fraction 7. Procedure
(m2).
6.5 Mix well all the 1.18 3 0.60 mm (No. 16 3 30) material 7.1 Clean the grindability machine thoroughly, place the
machine on a level surface, and space the balls as evenly as
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evenly in the grinding bowl, brushing any material that falls on A5.4.3 and report to the nearest whole number.
the elevated section of the lower grinding element into the 8.2 For ease of comparison between or among laboratories,
lower grinding element, which contains the balls. Fasten the calculate and report the percent residual moisture in the 1.18 3
bowl in position and make sure the load is fully applied to the 0.60 mm (No. 16 3 30) sample (Annex A6).
driving spindle. 8.3 Calculate the % Yield of 1.18 3 0.60 mm (No. 16 3 30)
7.3 Operate the machine for the specified 60.00 6 0.25 material generated from the initial 1000 g of 4.75-mm (No. 4)
revolutions. top-size sample and compare the actual value to a typical
7.4 Remove the bowl from the machine, lift out the upper median value (4.8.1) to gage the effectiveness/efficiency of the
grinding ring, and carefully brush adhering coal dust from the stage-crusher and of the stage-crushing process.
bowl and grinding ring onto a 16-mm [5⁄8-in.] sieve nested on m2
a 75-µm (No. 200) sieve and a closely fitting receiving pan. Y 5 m 3 100 (1)
1
Carefully empty the contents of the bowl onto the 16-mm
[5⁄8-in.] sieve. Brush off material adhering to the balls and where:
remove the balls from the 16-mm [5⁄8-in.] sieve. Brush material Y = % Yield,
adhering to the 16-mm [5⁄8-in.] sieve, including the underside m1 = mass of air dried sample (6.2), and
of the sieve, onto the 75-µm (No. 200) sieve. Replace the m2 = mass of 1.18 3 0.60 mm (No. 16 3 30) material
16-mm [5⁄8-in.] sieve with a close-fitting cover and shake the (6.4).
nested 75-µm (No. 200) sieve; cover and pan for 10 min 6 10 8.4 If other than primary HGI RMs are used for calibration
s in a mechanical sieving machine. After the 10-min 6 10-s of the test apparatus and method, report the source of the
period, carefully brush coal dust from the underside of the calibration standards used.
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ANNEXES
(Mandatory Information)
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A4. METHOD FOR DETERMINING THE HARDGROVE GRINDABILITY INDEX TO BE ASSIGNED TO EACH LOT OF THE
CANDIDATE HGI REFERENCE MATERIALS
(HGI RMs)
A4.1 Scope A4.3.2 Prepare a test sample from each of the four sub-
A4.1.1 This method describes the procedures used to test samples in accordance with Section 6.
the candidate Hardgrove Grindability Index (HGI) reference A4.3.3 Process each of the four subsamples in the grind-
materials (candidate HGI RMs) to obtain the HGI value to be ability machine in accordance with Section 7 and note the mass
assigned to that lot. of the original sample (50 g) minus the mass of the material
A4.1.2 Recognition to test the candidate primary HGI RMs retained on the 75-µm (No. 200) sieve.
for use in determining the HGI of coal (or for calibrating A4.3.4 (Primary HGI RMs)—To the nearest 0.1 HGI unit,
national HGI machines) is given by ASTM Committee D05 on determine the value of Hardgrove Grindability Index for each
Coal and Coke. subsample from the equation of the line (least squares regres-
sion line) or from the standardization graph derived from the
A4.1.3 Authority to test the candidate secondary HGI RMs
correlation of data between the standardization equipment
for use in determining the HGI of coal is given by the pertinent
reserved exclusively for HGI RM standardization purposes and
ISO national member body (NMB), which maintains oversight
the original equipment previously used by the Babcock &
responsibility for these activities.
Wilcox Co. (the “Hardgrove” sieve) for standard samples.
A4.3.5 (Secondary HGI RMs)—To the nearest 0.1 HGI unit,
A4.2 Apparatus
determine the value of Hardgrove Grindability Index for each
A4.2.1 All apparatus and equipment is essentially as pre- subsample from the equation of the line (least squares regres-
scribed in Section 4 but with the following special precautions sion line) or from the standardization graph derived from the
being taken: correlation of data between the standardization equipment
A4.2.1.1 A mechanical sieving machine (4.9) and a grind- reserved exclusively for HGI RM standardization purposes and
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ability machine (4.10) are both to be reserved for use only for the set of four primary HGI RMs obtained from the primary
determining HGI of the candidate HGI RMs. HGI RM producer.5
A4.2.1.2 At least four specially calibrated, stainless steel A4.3.6 Calculate the average and the standard deviation of
75-µm (No. 200) square-mesh sieves shall be set aside for use the four values obtained in A4.3.4 or A4.3.5 and report the HGI
only in determining the HGI of the HGI RMs [that is, in to the nearest whole number and the standard deviation to the
determining the amount of material passing the 75-µm (No. nearest 0.1 unit. Assign this average whole-number HGI value
200) sieve in 7.5]. One of the sieves (the primary “master” to the remaining HGI RMs in that lot.
sieve) is used only to check the secondary sieve, as needed. A4.3.7 (Primary HGI RMs)—Report the average value and
The secondary sieve is used to check the two (or more) the standard deviation (as well as individual analyses, analyst
working sieves at least annually. The two (or more) working identity, container identity, sieve identity, etc.) to the chairman
sieves are to be used only for determining HGI to be assigned of the ASTM D05.07 Producer Liaison Task Group.
to the the candidate HGI RMs. A4.3.8 (Secondary HGI RMs)—Report the average value
and the standard deviation (as well as individual analyses,
A4.3 Determination of Grindability Index of Each Lot of analyst identity, container identity, sieve identity, etc.) to the
HGI Reference Materials chairman of the pertinent NMB oversight committee.
A4.3.1 Randomly select four of the containers remaining
5
after the process defined in Annex A3 has been completed and The sole source of supply of the primary HGI reference materials (HGI RMs)
recognized by the committee at this time are available from The Pennsylvania State
the lot has been deemed to be homogeneous. University. Contact Brad Maben; Address: EMS Energy Institute, Pennsylvania
A4.3.1.1 In the special case of whenever the number of State Univeristy, C-211 CUL, University Park, PA US 16802; Telephone: +1-814-
containers in a lot is 24, randomly select and riffle-divide two 865–3899 (back up Telephone: +1-814-863-8896); Fax: +1-814-863-7432; email:
bam17@psu.edu; web-site: www.energy.psu.edu/HGI/index.html. ASTM Subcom-
containers from each given lot of candidate HGI RMs resulting mittee D05.07 and the ASTM/DOE Liaison Task Group maintains oversight for
from the process defined in Annex A2. Each of the four production of only the HGI RMs. Secondary standard reference samples are
resulting samples is tested for HGI according to the method available from other sources. If you are aware of alternative suppliers, please
provide this information to ASTM International Headquarters. Your comments will
described in the body of this test method. (Two different
receive careful consideration at a meeting of the responsible technical committee,1
technicians shall each test one portion obtained from each of which you may attend.
the two selected samples.)
A5.1 Scope A5.4.3 By the method of the sum of least squares, determine
A5.1.1 This method describes the procedure used to cali- the equation of the line that best fits the analytical results
brate Hardgrove machines. obtained from the four HGI RMs. An example HGI calculation
A5.1.2 Such Hardgrove machines can be used by pertinent from HGI RM data, shown in Table A5.1, illustrates this
ISO national member bodies (NMB) to assign values to lots of method.
candidate secondary HGI RMs. (See Annex A4.) A5.4.3.1 Example—Sum of Least Squares Fit—The equa-
A5.1.3 Such Hardgrove machines can be used by coal- tion of the line for the sum of least squares takes the form of:
analysis laboratories, which are then used for determining the Y 5 a 1 bX (A5.1)
HGI of coal.
where:
A5.2 HGI Reference Materials (HGI RMs) for Y = HGI,
Calibration5 a = y axis intercept,
A5.2.1 Four HGI RMs prepared especially for this purpose b = slope of the regression line, and
X = calculated −75-µm (−No. 200) material.
(in accordance with Annex A1-Annex A4) and representing
(1) a and b can be determined by use of the following table
grindability indices of approximately 40, 60, 80, and 100 shall
and equations:
be used for calibration.
Y X X2 XY
A5.2.2 Upon receipt, each of the HGI RMs should be 40 4.35 18.92 174.00
examined for the following: 58 7.14 50.98 414.12
A5.2.2.1 Preparation date (no more than six months old). 83 10.44 108.99 866.52
100 13.38 179.02 1338.00
A5.2.2.2 Oversize (material retained on a 4.75-mm (No.4 (Y = 281 (X = 35.31 ((X2) = 357.91 ((XY) = 2792.64
in.) sieve). {Less than 5 % +4.75 mm (No. 4.) and no particle
on a 6.30-mm [1⁄4-in. square-holed sieve]}. (Y(X2 2 (X(XY
a5 (A5.2)
A5.2.2.3 Foreign, noncoal material (no wood, rock, slate, n(X2 2 ~ (X!2
and so forth).
A5.2.2.4 Excessive fines [more than 30% −0.60-mm (−No. n(XY 2 (X(Y
b5 (A5.3)
30) material]. n(X2 2 ~ (X!2
A5.2.3 Whenever any of these parameters are unacceptable,
contact the agency responsible for production of the HGI RMs where:
(Y = 281,
and report the data on the response form accompanying the
(X = 35.31,
HGI RMs (see A5.4.4). ((X2) = 357.91,
A5.3 Apparatus ((XY) = 2792.64,
((X)2 = 1246.80, and
A5.3.1 All apparatus and equipment is that described in n = 4.
Section 4. (2) By doing these calculations, a = 10.63 and b = 6.75.
A5.4 Calibration Therefore, the equation of the line for this database is
HGI = 10.63 + 6.75 (calculated −75-µm (−No. 200) material).
A5.4.1 Calibrate each grindability machine, together with
A5.4.3.2 Use results from HGI RMs processed in accor-
all ancillary equipment including sieves (4.7) and plate mill
dance with Sections 6 and 7 in determining the equation of the
crusher (4.8), that will be used for this test when new, modified,
line by the sum of least squares method and (optionally) in
repaired, suspected of being defective, or when operated by
preparing the calibration chart (see Fig. A5.1).
new personnel.
A5.4.4 (Primary HGI RMs)—A standard form for reporting
A5.4.1.1 HGI RMs shall not be used for calibration beyond
data obtained during calibration is received with each set of
18 months from their preparation date. It is good practice to
HGI RMs received from the producer of the primary HGI
check the calibration of the HGI apparatus periodically with at
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least one of the HGI RMs (quality control check sample) even
if none of the conditions in A5.4.1 apply. This will ensure that TABLE A5.1 Example HGI Data Calculation—Actual Mass of
the system is still in control and it will allow for detection of Materials, g
problems previously unnoticed or not then occurring, and it Calculated,
+75 µm –75 µm
will allow for use of the HGI RMs before their expiration date. HGIA mass, iB
(+No. 200) (–No. 200)
Recovered Lost –75 µm
A5.4.2 For each calibration, process each of the four HGI (–No. 200)
RMs with indices of approximately 40, 60, 80, and 100 as 40 50.00 45.65 4.27 49.92 0.08 4.35
58 50.00 42.86 7.11 49.97 0.03 7.14
described in Sections 6 and 7 and use the results to determine 83 50.00 39.56 10.23 49.79 0.21 10.44
the equation of the line by use of the sum of least squares 100 49.99 36.61 13.25 49.86 0.13 13.38
method (A5.4.3) and, if desired, to prepare a calibration chart A
Value issued with HGI RMs.
(A5.4.3.1). B
Initial mass, g.
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NOTE—Example: Use certified HGI RM and develop a similar calibration chart(s) for each HGI apparatus, or sieve sets, or both.
FIG. A5.1 Example Calibration Chart
RMs.5 This form shall be completed and returned to the tion chart/equation) shall be verified against primary HGI
producer of the primary HGI RMs as noted on the form. A copy reference materials (HGI RMs). Where the calibration has
of this form is sent by the producer of the primary HGI RMs changed, the national Hardgrove machine will be recalibrated
to the ASTM D05 Producer Liaison Task Group for use in against the primary HGI RMs and a new calibration curve/
monitoring the primary HGI RMs. equation of the line determined and used.
A5.5 Verification/Recalibration
A5.5.1 At a period of no longer than 36 months, the
calibration of a national Hardgrove machine (with its calibra-
A6. METHOD FOR DETERMINING THE MOISTURE CONTENT OF THE 1.18 3 0.60 mm (No. 16 3 30) TEST SAMPLE
(Moisture Content)
A6.1 Scope air in the desiccator is dry to a moisture content of 1.9 mg/L or less. Values
in parentheses ( ) are literature values for the residual amount of moisture
A6.1.1 This method describes the procedures used to deter- in air at equilibrium with these desiccants.
mine the moisture content of the 1.18 3 0.60-mm (No. 16 3 NOTE A6.2—Warning: Sulfuric acid is corrosive and can cause severe
30) test sample. damage to eyes, skin, and clothing. Magnesium perchlorate is a strong
oxidant and can react violently with organic materials.
A6.2 Apparatus
A6.2.1 Drying Oven, Minimum Free Space [for moisture in A6.4 Moisture in the 1.18 3 0.60-mm (No. 16 3 30) Test
the 1.18 3 0.60-mm (No. 16 3 30) sample]—The oven shall Sample
be so constructed as to have a uniform temperature in all parts, A6.4.1 Heat an empty weighing dish under the conditions at
have a minimum of air space, and be capable of temperature which the 10-g sample is to be dried, place the cover on the
regulation between the limits of 104 and 110 °C [220 and weighing dish, cool the cover and dish in the desiccator until
230 °F]. Provision shall be made for renewing the preheated air the dish has cooled to ambient temperature, and weigh the dish
in the oven at a flow-rate of between approximately 2 to 4 and cover to 6 0.1 mg (m11).
times the oven volumes per minute. A6.4.2 Place the cover on the balance and the weighing dish
A6.2.2 Weighing Dish [for moisture in the 1.18 3 0.60-mm on the cover. Tare the balance (so the balance reads 0.0000 g).
(No. 16 3 30) sample] —Shallow, of glass, porcelain, fused With a spatula, collect increments from the unused 1.18 3
silica, or of corrosion-resistant metal, with a well-fitting cover, 0.60-mm (No. 16 3 No. 30) sieve size dedusted material until
of such a size that the coal layer does not exceed 0.20 g/cm2. approximately 10 6 0.1 g of the sample is in the weighing dish.
The dish should be as shallow as possible, consistent with Distribute the 10 g of sample evenly in the weighing dish.
convenient handling. Weigh the dish, cover, and sample (the “assembly”) at once to
A6.2.3 Desiccator, or similar cooling vessel—Adequate for 6 0.1 mg (m12).
allowing cooling of the dried, 10-g, 1.18 3 0.60-mm (No. 16 A6.4.3 Place the assembly near the drying oven, remove the
3 30) sample after the 90-min heating period and before cover, and place the uncovered weighing dish and sample into
weighing back of the dried sample; the desiccator must be the preheated drying oven 107 6 3°C [225 6 5°F]. Close the
adequately designed and maintained as to prevent moisture oven at once and heat for 90 min.
reabsorption/readsorption during cooling. A6.4.4 After 90 minutes, open the drying oven, quickly
A6.2.4 Analytical Balance [for moisture in the 1.18 3 remove and cover the weighing dish and dried sample, place
0.60-mm (No. 16 3 30) sample]—With an approximate the assembly into the desiccator, cool the assembly in the
capacity of at least 100 g, capable of weighing to the nearest desiccator, and weigh the assembly to 6 0.1 mg (m13) as soon
0.1 mg. as the assembly has cooled to ambient temperature.
A6.2.5 Calibration Weights—These calibration weights A6.5 Calculation and Report
shall be used to monitor the response of each balance over the
working range, as required by the laboratory’s quality system. A6.5.1 For ease of comparison between or among labora-
tories, calculate and report the percent moisture in the
A6.3 Reagents 1.1830.60 mm (No. 16 3 30) sample to the nearest 0.01%.
A6.3.1 Dry Air—Air used to purge the drying oven should A6.5.2 Calculate percent moisture in the 1.18 3 0.60-mm
be dried to a moisture content of 1.9 mg/L or less (to a dew (No. 16 3 30) material, M, as follows:
point of 10 °C or less, that is, 30 % relative humidity or less).
Any desiccant or drying method capable of achieving this M5 F m12 G
m12 – ~m13 – m11!
* 100 (A6.1)
degree of dryness is suitable.
A6.3.2 Desiccants—Materials suitable for use in the desic- where:
M = percent moisture in the 1.18 3 0.60-mm (No. 16 3
cator may be chosen from the following:
30) sample, %,
A6.3.2.1 Anhydrous Calcium Sulfate, (0.004 mg/L).
m11 = the mass of the empty weighing dish and cover, g,
A6.3.2.2 Silica Gel. m12 = the mass of the 1.18 3 0.60-mm (No. 16 3 30)
A6.3.2.3 Magnesium Perchlorate, (0.0005 mg/L). sample used, g, and
A6.3.2.4 Sulfuric Acid, Concentrated, (0.003 mg/L). m13 = the mass of the assembly after heating and cooling,
NOTE A6.1—The desiccant must be kept fresh enough to assure that the g.
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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 International 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
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