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Coal Rheology - A Practical Approach For Industry
Coal Rheology - A Practical Approach For Industry
Coal Rheology - A Practical Approach For Industry
INTRODUCTION
For metallurgical coals, rheology is routinely measured to understand their respective caking abilities during the coking
process. Both fluidity and dilatation parameters can be used to establish coals freshness and to monitor aging phenomena
when coals are stockpiled. At ArcelorMittal Dofasco (AMD), as coal brands can be stockpiled up to four months when the
shipping season is closed, coal rheology is measured on a weekly basis to establish if any potential coal aging issues arise.
This paper will propose a practical approach to the rheology data to help improve the interpretation of these test results for
coke plant operations.
BACKGROUND
Coal rheology is a measurement of a bituminous coal’s ability to soften, swell and resolidify into a semi-coke when heated.
This is a fundamental characteristic describing the caking ability of a coal, which allows it to transform into coke in a coke
oven. What is key in making an acceptable quality coke is that coal components have to soften and swell, and that
temperature ranges where individual reactive components soften and swell overlap to create a strong coke matrix. To
determine these characteristics, two ASTM tests are performed: Gieseler Plastometer and Dilatometer (Table 1). Further
details on these tests can be found in the ASTM Standards Volume 05.06(1)
All the coals that are used have a reasonable shelf life, but the HV “C” does have limited storage time. The last shipment of
this coal for the year is delivered in December and is used up by mid-February, when a three-coal blend is used. Routinely
measuring the extent of coal aging is very important when the coal has to be stockpiled for four months. This paper discusses
how AMD handles the interpretation of the data generated.
Gieseler Platometer
The Gieseler plastometer is used to measure the plastic properties of a given coal. The apparatus used is shown in Appendix
1. For this test, coal of a specific size (100% -0.425mm) is placed in a crucible with a rabble arm stirrer and assembly heated
at 3°C/minute up to 550°C. A constant torque is applied to the stirrer. The latter will not rotate until the coal begins to soften
and will continue to rotate “freely” until the coal mass has resolidified upon further heating. This stirrer rotation rate is the
total dial divisions undergone by the stirrer in one minute, or better known as ddpm. There are 100 dial divisions for each
360° of rotation. A typical Gieseler plastometer output is shown in Figure 1.
The temperature at which a given coal softens (T1), reaches maximum fluidity or maximum stirring rate (T2), and resolidifies
(T3) are measured. The difference between the resolidification and softening temperature is defined as the temperature
range.
The property/parameter most often reported is the maximum ddpm of a given coal. Also noted are the T1 (Tsof), T2 (Tmax)
and T3 (Tresol) temperatures shown in Figure 1. The issue is that the maximum fluidity is not always the best indicator of the
degree of coal “aging” and can cause a false negative. The actual ddpm can be quite variable for many reasons, most notably
the original head sample size, size consist, petrographic makeup of the test sample itself and possible issues of coal jamming
and breaking during heating in the plastometer retort. For the AMD sample, a small cut from a daily sample is collected so
this may not be truly representative but will provide a data point in time. Data trends are plotted over the given year to
determine if the coals being used have any detectable aging issues.
Figure 10. Dilatometer Results for HV "B" with both Dilatation and Temperature Range
Similar to the response for the Gieseler values, if the temperature range is in an acceptable range, no further testing is
required for that week. If both the dilatation and temperature range are suspect, then again, a sample from the next day is
tested to confirm.
For the HV "C" coal, the dilatation results including temperature range are shown in Figure 11. This coal, which is a low
rank component of the AMD blend is expected to have a short shelf life. As the coal pile diminishes towards the middle of
winter, there are concerns about coal age and its impact on coke ambient strength and CSR. Knowing if there will be any
issues is imperative to operations since AMD uses this component at 25% of the blend.
NEXT STEPS
As mentioned previously, coal rheology properties will be a function of coal grain size, coal petrographic properties, i.e.
reactive types and amounts, inert types and amounts and the reactivity of the semi-fusinite, bulk density of the coal sample,
heating rate, etc. For the standard rheology tests, a constant heating rate of 3°C per minute is used so that fixes this
parameter.
Both the Gieseler and dilatometer tests require the test sample to be stage crushed to pass 40 and 60 mesh screens,
respectively. The standards do not state lower limits for sample screen size, just that it must pass. Is it possible then that one
coal could contain for example greater percentage of say -100 mesh material than another coal? If this occurs and surely does
so from differences observed in HGI test among coals, one can then expect various results compared to say a test sample that
has lower percentage of -100 mesh.
In fact, considering the hardness (HGI) differences measured for low, medium and high volatile coals, there will certainly be
various size distributions used in a rheology test. In processing the test samples, laboratories use pulverization equipment to
crush the material to pass the required sieve for that test. As long as the sample passes the required mesh size, it is not
CONCLUSIONS
1. Both maximum fluidity and dilatation are good indicators of a coal’s plastic properties and ability to coke but can
exhibit appreciable variability.
2. The measured temperature ranges from these tests is a much more stable and better indicator of a coal’s extent of
aging.
3. For both the Gieseler plastometer and dilatometer tests, the Maximum Fluidity and % Dilatation should continue to
be reported, but the temperature range should also be reported in the test sample report.
4. The temperature range should be used to determine if a second test sample need be collected and tested.
5. To trigger the decision for carrying out a retest, the suggested minimum temperature ranges should be used in
conjunction with the Maximum Fluidity and % Dilatation.
6. It is suggested that the control limits for rheology tests should be reevaluated perhaps annually for each coal brand.
REFERENCE
1. ASTM Volume 05.06 – Gaseous Fuels: Coal and Coke; Catalysts; Bioenergy and Industrial Chemicals from Biomass