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Notes<br />

1773<br />

0.022<br />

30<br />

0.020<br />

i b 0.019<br />

c -<br />

5 0.016<br />

E<br />

- 0.017<br />

2<br />

0.016<br />

I<br />

0.015<br />

25<br />

I<br />

2 20<br />

0<br />

c g 15<br />

8<br />

2<br />

10<br />

5<br />

Corrected Velocity _<br />

0.014<br />

u 5 10 15 20 25 30 35 40<br />

Salinity, 20<br />

0 A<br />

0<br />

30 40 50 60<br />

Rodius. cm<br />

Fig. 5. Calculated concentration difference of CaSO,<br />

between the solid-liquid interface and bulk solution of<br />

clod cards in natural seawater sources based on Eq. 7.<br />

Curve A was calculated based on literature values of seawater<br />

chemical content at 32%1 and assuming that seawater<br />

was diluted with distilled water to achieve the lower salinities;<br />

curve B was calculated based on chemical analyses<br />

of Puerto Peiiasco seawater at 40?&0 and Tucson tapwater<br />

used as the diluent in our study.<br />

Ac =<br />

1(<br />

_<br />

[Ca2+lb + W42% 2 + K Oo5<br />

2 1<br />

SP<br />

I<br />

Ka2+lb + W42- lb<br />

2 ) . (7)<br />

[Ca2+]i, [Ca2+lb, [S042-]i, and [S042-]b are calcium<br />

and sulfate ion concentrations at the interface<br />

and in the bulk solution. Ksp is the solubility<br />

product, which can be computed by the<br />

expressions given by Marshall and Slusher<br />

(1968), who allow for the presence of ion pairs<br />

such as MgS040 in their correlations.<br />

The values of [Ca2+16 and [S042-]b used in<br />

Eq. 7 are based on the total calcium and sulfate<br />

measured in solution; we have made no attempt<br />

to correct these concentrations for the<br />

presence of ion pairs containing calcium or<br />

sulfate. Increasing the ionic strength (or salinity)<br />

increases the CaSO, solubility product,<br />

thereby increasing the gradient between the interface<br />

and the bulk solution and accelerating<br />

the dissolution rate of a clod card. However,<br />

this effect is counteracted if the concentration<br />

of CaSO, in the bulk solution increases with<br />

salinity, which is the case with seawater; the<br />

seawater used in our experiments contained<br />

CaSO, at concentrations more than eight times<br />

that of the freshwater supply. The brackish<br />

supply, prepared by dilution, was intermediate.<br />

Figure 5 contains salinity correction curves<br />

Fig. 6. Correction for the induced-water-motion effect<br />

of the rotating arm in the tank. Top line is the velocity of<br />

the clod card in the tank at each position on the arm;<br />

bottom line is the velocity of the water in the tank estimated<br />

by the movement of suspended particles in the<br />

water; middle line is the corrected velocity used to correlate<br />

the card dissolution rates with water motion.<br />

based on Puerto Peiiasco seawater and Tucson<br />

tapwater used in our study (curve B) and on<br />

literature values of normal seawater constituents<br />

(Hansson 1973) assumed to be diluted<br />

with distilled water (curve A). Curve B falls<br />

below curve A because Tucson tapwater and<br />

Puerto Pefiasco seawater contain proportionally<br />

more CaSO, than distilled water and standard<br />

seawater.<br />

The water motion tank was used to obtain<br />

data for velocity-weight loss correlations. The<br />

velocity of the clod card through the water was<br />

easily calculated from the rotation rate of the<br />

arm and the distance of the card from the center<br />

of rotation. However, it was necessary to<br />

correct for the rotary movement imparted to<br />

the water in the tank by the moving arm. This<br />

movement was determined at each of the five<br />

positions by measuring the movement of small<br />

suspended particles in the water. A drag model<br />

was correlated to the data and used to correct<br />

the velocities of the cards into estimates of<br />

their velocities relative to the water at each<br />

position (Fig. 6). The correction was more significant<br />

at low than at high velocities.<br />

Forced convection tests were run at temperatures<br />

from 13 to 35°C in three different<br />

salinities on the rotating arm (Fig. 7). Plots in<br />

the form of Eq. 5 were subjected to regression<br />

analyses (Table 2). In all runs, clod card weight<br />

loss at the lowest test velocity was increased<br />

by free convection, and the points fell - 15%<br />

above the curve of best fit to the other points;

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