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1. Introduction - Firenze University Press

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p<br />

p<br />

1 <strong>1.</strong><br />

5<br />

p <br />

H 1 <strong>1.</strong><br />

5<br />

2O<br />

p<br />

mixture <br />

H<br />

, using<br />

2O<br />

H 2O<br />

p <br />

1 <br />

1 <br />

p<br />

p<br />

With input values H2O = 1002.7*10 -6 Pa*s, slag=2604 kg/m 3 and solvent =1008 kg/m 3 , (4) yields<br />

mixture= 1102*10 -6 Pa*s. Together with =1074 kg/m 3 , and with experimental values n=5 1/s and<br />

d=0.09 m, Rev =3947<strong>1.</strong> In other words, the mixing situation is clearly turbulent. Power number in a<br />

vessel without baffles for a turbine stirrer is then estimated to <strong>1.</strong>25, resulting finally to energy<br />

dissipation of 0.076 W/kgsolution. In a fully baffled reactor, resulting to better mixing, the power<br />

number would be approximately 6, yielding to 0.369 W/kgsolution [16].<br />

If it is further assumed that the ratio of mixer diameter and vessel volume is maintained constant in<br />

scale-up, this means that plainly mixing of slag and ammonium salt solvent in extraction requires<br />

20.8 kW/25 ton slag, or 0.8 kW/ton slag. Related to PCC production, this equals to <strong>1.</strong>9 kW/ton<br />

PCC. If the experimental residence times (Table 3) would be used for the larger scale, this would<br />

mean 0.8 kW/ton slag * (25/60) h = 0.33 kWh/ton slag. However, these numbers do not include the<br />

electrical losses of the system (90% efficiency would yield to 23.1 kW/ 25 ton slag), nor they are<br />

optimised considering the mixer dimensions and reactor size relation. When compared to heat<br />

duties of the different reactors (Table 8), it can be seen that also the mixing energy has a small, yet<br />

significant role for the overall energy balance of the process.<br />

For the carbonation reactor, the energy dissipation in mixing would be lower since the high gas<br />

flow through the reactor lowers the solution density and viscosity. Also, depending on the gas inlet<br />

arrangement, the mixing caused by the gas flow itself could be sufficient to obtain the required<br />

dispersion of solution components.<br />

5. Studies on additional process units<br />

5.<strong>1.</strong> Separation equipment<br />

As mentioned in Section 2.2, various options exist for continuous separation of solids from the<br />

aqueous streams. For steel slag separation, a gravitational settling tube (Fig. 7) was tested<br />

experimentally [18]. The utilised plastic tube with a circular cross-section had a volume of 8.64 L<br />

(length 110 cm, diameter 10 cm), and it was used with a feed flow of 40 L/h. The underflow was<br />

maintained at ~7 L/h, a value high enough to guarantee a steady stream for the concentrated particle<br />

suspension, resulting thus to an overflow of 33 L/h.<br />

The feasibility of using the settling tube was tested with spherical Ballotini glass beads (p = 2634<br />

kg/m 3 , d p = 163 µm) in water. Tests were performed with the settling tube positioned horizontally<br />

(0°) and at an angle of 10°. The beads settled within 0-22 cm from the feed orifice on the horizontal<br />

tube and approximately within the same range in the tube with 10° angle. The distances where the<br />

settling occurred were observed visually during the experiments. Because of the large size and high<br />

density of the glass beads the separation efficiency was ~100%.<br />

To obtain an estimate with separation efficiencies with the actual steel slag, tests were performed<br />

with the steel converter slag (p = 2604 kg/m 3 , d p = 96 µm) that was used also as an input material<br />

for the modelling work described in Section 2. Angles of 30° and 45° were used with water as the<br />

liquid phase, but 45° was tested also with 1 mol/L NH4Cl. Sedimentation was observed between 0-<br />

83 cm (0-80 cm for 45°), although the determination was quite challenging due to a very turbid<br />

suspension.<br />

After the process had reached a steady-state, a sample was taken from the outflow to determine the<br />

concentration of particles. The samples were filtrated, dried in an oven at 105 °C and weighed.<br />

Calculated from (5), the separation efficiencies were 99.9% for both 30° and 45° experiments.<br />

228<br />

H 2O<br />

(4)

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