Water and Solute Permeability of Plant Cuticles: Measurement and ...
Water and Solute Permeability of Plant Cuticles: Measurement and ...
Water and Solute Permeability of Plant Cuticles: Measurement and ...
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52 2 Quantitative Description <strong>of</strong> Mass Transfer<br />
2. We use (2.9) <strong>and</strong> obtain the steady state fluxes <strong>of</strong> urea <strong>and</strong> sucrose across the cell<br />
wall as 1.38 × 10 −3 <strong>and</strong> 5.23 × 10 −4 molm −2 s −1 respectively.<br />
3. We solve this problem in four steps. (1) The amount <strong>of</strong> non-ionised 2,4-D in<br />
the donor is the product <strong>of</strong> mass (0.1 l = 0.1 kg) <strong>and</strong> concentration <strong>of</strong> donor<br />
(1 × 10 −3 moll −1 ), which is 1 × 10 −4 mol. (2) The concentration <strong>of</strong> 2,4-D in the<br />
cuticle can be calculated using (2.12). The concentration <strong>of</strong> 2,4-D in the cuticle<br />
is the product <strong>of</strong> the donor concentration (1 × 10 −3 molkg −1 ) <strong>and</strong> partition coefficient<br />
(600), which is 0.6molkg −1 . (3) The area <strong>of</strong> cuticle exposed to the donor<br />
was 1cm 2 <strong>and</strong> the thickness was 10µm, which results in a volume <strong>of</strong> cuticle <strong>of</strong><br />
1 × 10 −9 m 3 . With a specific weight <strong>of</strong> cuticle <strong>of</strong> 1,000kgm −3 , the mass <strong>of</strong> the<br />
cuticle exposed to the donor is 1 × 10 −6 kg. The amount <strong>of</strong> 2,4-D in the cuticle<br />
is the product <strong>of</strong> mass <strong>of</strong> cuticle times 2,4-D concentration in cuticle, which<br />
amounts to 6 × 10 −7 mol. (4) According to Fig. 2.7 the solute concentration in<br />
the cuticle during steady state is only half the maximum concentration. Hence,<br />
in the steady state 1 × 10 −4 mol2,4-D are in the donor, while only 3 × 10 −7 mol<br />
are sorbed in the cuticle. This is a negligible amount, <strong>and</strong> we can safely use the<br />
donor concentration <strong>of</strong> 1 × 10 −3 moll −1 in calculating permeance. However, it<br />
should be clear from the calculation that sorption in the cuticle would not have<br />
been negligible if the donor volume had been only 1 ml or less.<br />
4. From Fig. 2.9a we read the fractions <strong>of</strong> 2,4-D that would have been collected<br />
from the receiver, had we taken only one sample after the second (0.39) or the<br />
third day (0.53) respectively. Using (2.30) <strong>and</strong> these figures, we calculate the flow<br />
(F) in 2 days or 3 days as 2.25 × 10 −11 <strong>and</strong> 2.04 × 10 −11 mols −1 respectively.<br />
Before we can calculate P using (2.31), we must decide which donor concentration<br />
to use. We are ignorant, <strong>and</strong> use the initial concentration <strong>of</strong> 1molm −3 <strong>and</strong><br />
obtain a P <strong>of</strong> 2.25 × 10 −7 ms −1 if we terminated the experiment after 2 days, <strong>and</strong><br />
2.04 ×10 −7 ms −1 if the experiment lasted 3 days. The true P calculated from the<br />
rate constant k is 2.89 × 10 −7 ms −1 ; hence, we underestimated P by factors <strong>of</strong><br />
1.28 <strong>and</strong> 1.42 respectively. This may not seem a lot, but we must remember that<br />
the 2,4-D concentration <strong>of</strong> the receiver was zero throughout, because we used a<br />
pH <strong>of</strong> 9.2 <strong>and</strong> all 2,4-D molecules reaching the receiver were ionised. Without<br />
this trick, ∆C across the membrane would have been much smaller <strong>and</strong> the error<br />
in P much larger, the magnitude depending on the volume <strong>of</strong> the receiver.<br />
5. We use (2.34) to solve this problem, <strong>and</strong> obtain 55 h <strong>and</strong> 2,273 days respectively.