Abstract :
In modern urban atmosphere, sulphur dioxide SO2.attacks calcite CaCO3.in calcareous stone-producing gypsum
CaSO4P2H2O.which forms crust at rain sheltered surfaces and accelerates erosion at areas exposed to rain. The airborne
particles collected on stone surfaces have always been considered to enhance the gypsum crust formation and thus it is
believed that they should be removed from the surface to decrease the effects of SO2. In this study, our aim was to
investigate this event by carrying out a series of experiments in laboratory using pure calcium carbonate powder to represent
calcareous stone. Sodium montmorillonite, activated carbon, ferric oxide, vanadium pentoxide and cupric chloride were
mixed in the pure calcium carbonate powder as substitutes of the airborne particles in the polluted atmosphere. The samples
have been exposed at nearly 10 ppmv SO2 concentrations at 90% relative humidity conditions in a reaction chamber for
several days. The mineralogical composition of the exposed samples were determined by X-ray diffraction XRD.analysis
and infrared spectrometer IR.. Sulphation reaction products, calcium sulphite hemihydrate, gypsum and unreacted calcite,
were determined quantitatively using IR. Exposed samples have also been investigated morphologically using a scanning
electron microscope SEM.. Experimental results reveal that calcium sulphite hemihydrate is the main reaction product of
the SO2–calcite reaction. It turns out that airborne particles play an important catalytic role in the oxidation of calcium
sulphite hemihydrate into gypsum, although their presence does not very significantly affect the extent of sulphation
reaction. This behaviour of airborne particles is explained by the presence of liquid film on the calcium carbonate surface
where a series of reactions in the gas–liquid–solid interfaces takes place. q1999 Elsevier Science B.V. All rights reserved.
Keywords :
Sulphation , particulate matter , Sulphur Dioxide , calcite