Brown Coal Derived Pproducts for Ameliorating Soil Acidity
J Issa, A Patti and W Jackson Monash University, Melbourne
High acidity in soil is directly related to high toxic aluminium levels.
An increase in pH is desirable down to the root zone of crops (>10 cm).
Typical treatments such as lime and gypsum only increase pH near the soil
surface unless they are physically incorporated; this is labour and cost
intensive, and may also cause soil degradation.
Humic acid derived from brown coal, with added calcium, when applied
to the soil surface, can increase pH deeper into the soil profile.
The humates can move down with water percolating the soil. As they
move down, the added calcium bound to the humate’s cation exchange sites
(the acidic oxygen functional groups) can exchange with toxic aluminium
ions and ions on exchange sites in the soil. Thus the soil pH is
buffered, nutrient transport to plants assisted, and phytotoxic aluminium
bound and rendered harmless to plants.
Humic material fractions obtained from brown coal can be classified
according to their solubility in acid and base. These fractions differ
in their ability to decrease soil acidity. The ‘humin’ fraction (base-insoluble)
has a low acid group content and moves slowly through the soil. Humic
acid (base-soluble, acid-insoluble) and fulvic acid (base and acid-soluble)
move more rapidly; fulvic acid has more acidic groups than humic acid,
but its lower molecular weight makes it more susceptible to microbial degradation,
so that it is destroyed before benefiting the soil.
K Humate is a commercially available source of humate (ex HRL Agriculture
Pty Ltd, Australia) derived from brown coal. It can be obtained by
the treatment of brown coal with potassium hydroxide. Calsulmag is
a commercial treated coal fly ash (also ex HRL Agriculture Pty Ltd) which
can be used instead of lime due to its high inorganic calcium and magnesium
content. When K humate and Calsulmag are combined in an aqueous mixture,
and applied to the surface of an acidic soil, pH is increased (from 3.8
to 4.5) as is exchangeable calcium (30-50%), while exchangeable aluminium
is decreased (30-50%), down to a 5 cm depth.
Optimisation of Underground Coal Gasification for Improved Performance
and Reduced Environmental Impact
A Beath and C Mallett CSIRO Exploration and Mining, Brisbane
Development of improved UCG processes has been performed using two
complementary methods. The first of these is the utilisation of detailed
models of the gasification of coal under the conditions experienced in
UCG. The development of these models is discussed and the sensitivity
of the models to variables such as temperature, pressure, water ingress
and feed gas composition input is analysed. In the second stage of
the optimisation various process arrangements for the surface plant were
simulated using a commercial process modelling software package.
The objective was to determine process arrangements that had both high
efficiency and minimal emission of greenhouse gases. The processes
were all specifically designed for electricity generation, however the
techniques used could also be applied to synthesis gas production.
The preferred process developed allows for separate combustion of hydrogen,
with a stream comprised of methane, carbon monoxide and other gases being
burnt separately in oxygen, allowing for sequestration of a carbon dioxide
rich stream. Disposal of the carbon dioxide could possibly be in
spent underground gasification sites. As the majority of the gas
processing is carried out at high pressures, there is minimal expenditure
of energy in recompression of the carbon dioxide for sequestration.
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