ASTM D6307.2019 Determination of Asphalt Content by Ignition Method
ASTM D6307.2019 Determination of Asphalt Content by Ignition Method
ASTM D6307.2019 Determination of Asphalt Content by Ignition Method
for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Designation: D6307 − 19
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D6307 − 19
minimum openings of 3.35 mm and 600 µm, respectively, has been found the equipment used (for a particular method), the test specimen may be
to perform well. divided into suitable increments, tested, and the results combined for
calculation of asphalt content based on the weighted average of the masses
5.3 Catch Pan, of appropriate size to hold the sample trays used in the increments.
so that aggregate particles and melting asphalt binder falling
through the screen mesh are caught. 7.4 Obtain samples of asphalt cement in accordance with
Practice D140/D140M.
5.4 Catch Pan/Sample Tray(s) Handling Apparatus, suitable
for inserting catch pan and sample tray(s) into furnace and
removing hot catch pan and sample tray(s) from furnace. TEST METHOD A
5.5 Assorted Spatulas, Pans, Bowls, and Wire Brushes, for
preparing asphalt mixtures and removing aggregate from 8. Apparatus
sample tray(s) and catch pan. 8.1 In addition to the apparatus listed in Section 5, the
5.6 Protective Gloves, well insulated and capable of with- following apparatus is required for Test Method A.
standing 580 °C. 8.1.1 Ignition Furnace—A forced-air ignition furnace that
heats the sample by either convection method or direct
5.7 Ovens—Mechanical ovens, convection or forced draft,
irradiation method. The convection-type furnace must have a
shall be provided for drying aggregates and asphalt mixtures,
minimum temperature capability of 580 °C. The furnace shall
and for preheating asphalt mixtures prior to ignition testing.
have an internal weighing system capable of measuring the
5.8 Ignition Furnace, as described in 8.1.1 or 11.1.1. mass of sample sizes of at least 2500 g. The furnace chamber
shall be of sufficient size to accommodate sample sizes of at
6. Hazards least 2500 g. A data collection system also shall be included so
6.1 The temperature of the furnace, sample, sample tray(s), that the sample mass loss can be determined automatically to
and catch pan after removal from the furnace is extremely high. an accuracy of 0.1 g and displayed during a test. The test is
Caution, therefore, must be exercised at all times when deemed complete when the difference between consecutive
handling these items, as failure to do so could result in serious measured mass loss does not exceed 0.01 % of the sample mass
injury, severe burns, or fire. The sample, sample tray(s), and for three consecutive 1-min intervals. The equipment shall
catch pan should be placed inside a safety cage and should not provide a printout of the test results. A system capable of
be allowed to cool near any materials that are subject to reducing furnace emissions to an acceptable level also shall be
ignition at the high temperatures used in this procedure. The incorporated in the furnace. The furnace shall be vented into a
furnace manufacturer’s instruction manual must be followed to hood or to the outside and, when set up properly, will have no
take all necessary precautions. noticeable odors escaping into the laboratory. The furnace will
have a fan with the capability to pull air through the furnace to
7. Sampling expedite the test and to reduce escape of smoke into the
7.1 Obtain samples of aggregate in accordance with Practice laboratory. The furnace shall be equipped so that the door
D75/D75M. cannot be opened during the ignition test.
7.2 Obtain samples of asphalt mixture in accordance with 8.1.2 Filters, if required, of the type specified by the furnace
Practice D979/D979M and AASHTO R47. manufacturer.
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D6307 − 19
9.4.2 For the direct irradiation-type furnace, set the burn designed for samples that may not burn completely using the
profile to the DEFAULT mode. DEFAULT burn profile.
9.5 Heat the aggregates and asphalt cement to approxi- 9.16 The temperature or burn profile for testing asphalt
mately 150 °C. Heat all mixing bowls and tools to approxi- mixture samples in 10.3 shall be the same temperature or burn
mately 150 °C. profile selected for testing mixture calibration samples.
9.6 Prior to the mixing of calibration samples, an initial or 10. Procedure
“butter” mix is required to condition the mixing equipment. 10.1 Obtain an asphalt mixture sample in accordance with
Remove and discard the “butter” mix from the bowl by Section 7. The sample mass should be approximately the same
scraping, leaving a uniform coating of asphalt mix residue. as that used for calibration (9.2).
NOTE 4—The “butter” mix prevents calibration samples from being 10.2 Oven dry the asphalt mixture sample to constant mass
biased by residual asphalt mix retained in the mixing bowl. at a temperature of 110 6 5 °C or determine the moisture
9.7 Prepare three calibration samples at the design asphalt content of samples in accordance with Test Method D1461, so
cement content (P). Incorporate additives and modifiers, if any, that the measured mass loss can be corrected for moisture.
to be used. 10.3 Set the furnace temperature or burn profile in accor-
dance with Section 9. Samples can be placed in the furnace at
9.8 Determine and record the mass of the sample tray(s) and
significantly lower temperatures, since the furnace will quickly
catch pan to the nearest 0.1 g.
heat to the desired temperature once the sample begins to burn.
9.9 Evenly distribute the sample in the sample tray(s). The furnace temperature is likely to increase during the
ignition phase of the test.
9.10 Determine the mass of the sample, sample tray(s), and
catch pan to the nearest 0.1 g. Calculate and record the initial 10.4 Determine and record the mass of the sample tray(s)
mass of the sample (MI). and catch pan to the nearest 0.1 g.
9.11 Heat the calibration sample in the convection-type 10.5 Evenly distribute the sample in the sample tray(s).
furnace at 540 6 5 °C; or in the direct irradiation-type furnace 10.6 Determine the mass of the sample, sample tray(s), and
using the DEFAULT mode until the change in mass of the catch pan to the nearest 0.1 g. Calculate and record the initial
sample during three consecutive 1-min intervals does not mass of the sample (MB).
exceed 0.01 % of the sample mass (MI). 10.7 Heat the sample in the furnace at the specified tem-
9.12 Measure and record the mass (ML) of the sample after perature until the difference between consecutive measured
ignition to the nearest 0.1 g. The mass can be obtained mass loss does not exceed 0.01 % of the sample mass (MB) for
immediately upon completion of the test from the printout or three consecutive 1-min intervals. This point shall be deter-
display. mined automatically by the furnace’s data collection system.
9.13 Calculate the calibration factor (CF) as follows: 10.8 The furnace’s data collection system shall measure and
automatically record the aggregate mass (MA) of the sample
CF 5 S MI 2 ML
MI
3 100 2 PD (1) after ignition to the nearest 0.1 g. The mass shall be obtained
immediately upon completion of tests by subtracting the mass
where: loss measured by the furnace from the initial mass of the mix
MI = total mass of the mixture calibration sample prior to (MB).
ignition, 10.9 The corrected asphalt content shall be calculated auto-
ML = total mass of the mixture calibration sample after matically by the furnace’s data collection system as follows:
ignition, and
P = percentage of actual asphalt cement in the mix by mass
of the total mix expressed as a percentage.
% AC 5 S MB 2 MA
MB D
3 100 2 C F (2)
where:
9.14 Repeat steps 9.8 – 9.13 for two additional calibration
samples. Calculate the average calibration factor (CF) by AC = measured asphalt content percent by mass of the
averaging the three CF values. oven-dry asphalt mixture sample,
MA = total mass of aggregate remaining after ignition,
9.15 Calibration Temperature Adjustments: MB = total mass of the asphalt mixture sample prior to
9.15.1 For the convection-type furnace, if the calibration ignition, and
factor exceeds 1.0 %, lower the test temperature to 482 6 5 °C CF = calibration factor obtained in Section 9 and entered
and repeat steps 9.2 – 9.14 . Use the calibration factor obtained into the furnace’s data collection system.
at 482 °C, even if it exceeds 1.0 %.
9.15.2 For the direct irradiation-type furnace, the DE- TEST METHOD B
FAULT burn profile should be used for most materials. The
operator may select burn profile OPTION 1 or OPTION 2 to 11. Apparatus
optimize the burn cycle. OPTION 1 is designed for aggregates 11.1 In addition to the apparatus listed in Section 5, the
with a correction factor greater than 1.0 %. OPTION 2 is following apparatus is required for Test Method B.
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D6307 − 19
11.1.1 Furnace, having a minimum temperature capability 12.13 Remove the sample from the furnace and allow it to
of 580 °C and equipped with a fan capable of pulling air cool for at least 10 min.
through the furnace to expedite the test and to reduce escape of 12.14 Measure and record the mass (ML) of the sample after
smoke into the laboratory. The furnace chamber shall be of ignition to the nearest 0.1 g.
sufficient size to accommodate samples sizes of at least 2500 g.
A system capable of reducing furnace emissions to an accept- 12.15 Place the sample back into the furnace.
able level also shall be incorporated in the furnace. The furnace 12.16 After the furnace reaches the set-point temperature,
shall be vented into a hood or to the outside and, when set up heat the calibration sample for 15 min.
properly, will have no noticeable odors escaping into the
12.17 Remove the sample from the furnace and allow it to
laboratory. The furnace shall be equipped so that the door
cool for at least 10 min.
cannot be opened during the ignition test.
11.1.2 Filters, if required, of the type specified by the 12.18 Measure and record the mass (ML) of the sample after
furnace manufacturer. ignition to the nearest 0.1 g.
12.19 Repeat 12.15 – 12.18 until the change in measured
12. Calibration mass (ML) of the sample after ignition does not exceed 0.01 %
12.1 The results of this test method may be affected by the of the initial sample mass (MI).
type of aggregate in the mixture because different aggregates 12.20 Record the last value obtained for (ML) as the mass
lose mass on ignition to varying degrees. The results may also (ML) of the sample after ignition.
be affected by the presence of additives and modifiers in the 12.21 Calculate the calibration factor (CF) as follows:
asphalt mixture sample. Accordingly, to optimize accuracy, a
calibration factor shall be established by testing three calibra-
tion samples for each mix type. The calibration shall be
CF 5 S MI 2 ML
MI D
3 100 2 P (3)
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13.7 Heat the asphalt mixture sample in the furnace at 540 14. Report
6 5 °C for at least 45 min. 14.1 Report the following information:
13.8 Remove the sample from the furnace after ignition and 14.1.1 Date,
allow it to cool for at least 10 min. 14.1.2 Identification of aggregate and mix type,
14.1.3 Test number,
13.9 Measure and record the mass (MA) of the sample after
14.1.4 Calibration data,
ignition to the nearest 0.1 g.
14.1.5 Mass of the asphalt mixture sample before and after
13.10 Place the sample back into the furnace. ignition (nearest 0.1 g),
13.11 After the furnace reaches the set-point temperature, 14.1.6 Measured asphalt content (nearest 0.01 %), and
heat the sample for at least 15 min. 14.1.7 Aggregate gradation, if performed.
13.12 Remove the sample from the furnace and allow it to 15. Precision and Bias
cool for at least 10 min. 15.1 The single-laboratory standard deviation for asphalt
13.13 Measure and record the mass (MA) of the sample after content has been found to be 0.04 %; therefore, results of two
ignition to the nearest 0.1 g. properly conducted tests by the same operator on the same
aliquot samples of the asphalt mixture should not differ by
13.14 Repeat 13.10 – 13.13 until the change in measured more than 0.11 % (Notes 7-9).
mass (MA) of the sample after ignition does not exceed 0.01 %
of the initial sample mass (MB). 15.2 The multi-laboratory standard deviation for asphalt
content has been found to be 0.06 %; therefore, the results of
13.15 Record the last value obtained for (MA) as the mass two properly conducted tests from two different laboratories on
(MA) of the sample after ignition. asphalt mixture samples from the same batch should not differ
NOTE 6—Steps 13.10 – 13.15 may not be necessary if it can be by more than 0.17 % (Notes 7-9).
demonstrated from the mix calibration data that constant mass could be 15.3 The bias for this test method is currently under
achieved by heating the sample only once in the furnace. The type and
mass of the asphalt mixture sample being tested should be reasonably development.
close to those of the calibration sample. NOTE 7—These numbers represent, respectively, the (1S) and (D2S)
13.16 Calculate the corrected asphalt content as follows: limits described in Practice C670.
NOTE 8—These precision statements are based on four aggregate types,
% AC S MB 2 MA
MB D
3 100 2 C F (4)
four replicates, and twelve laboratories participating with no laboratory
results deleted as outlying observations. All four aggregates had relatively
low absorption values (water absorption values ranging from 0.5 to
where: 0.8 %).
AC = measured asphalt content percent by mass of the NOTE 9—These precision statements are applicable to Test Method A
only, using laboratory prepared mixtures (not plant-mixed pavement
oven-dry asphalt mixture sample,
samples). The precision of Test Method B has not been determined.
MA = total mass of aggregate remaining after ignition,
MB = total mass of the asphalt mixture sample prior to 16. Keywords
ignition, and 16.1 asphalt content; asphalt paving mixtures; ignition
CF = calibration factor, obtained in Section 12.
method
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