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Water and Solute Permeability of Plant Cuticles: Measurement and ...

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7.1 Sorption <strong>of</strong> Plasticisers in Wax <strong>and</strong> Cutin 211<br />

K ww<br />

10 5<br />

10 4<br />

10 3<br />

10 2<br />

10 1<br />

10 0<br />

10 −1<br />

10−2 10−1 C 4E 2<br />

10 0<br />

10 1<br />

C 8E 4<br />

C 6E 3<br />

10 2<br />

C 12E 8<br />

K mxw<br />

C 10E 5<br />

10 3<br />

C 14E 7<br />

C 12E 6<br />

10 4<br />

C 16E 8<br />

10 5 10 6<br />

Fig. 7.3 Correlation between wax/water partition coefficients (Kww) <strong>and</strong> cuticle/water partition<br />

coefficients (Kmxw). Redrawn from Schreiber et al. (1996b)<br />

Reconstituted waxes from barley <strong>and</strong> Chenopodium leaves are solid <strong>and</strong> partially<br />

crystalline phases, <strong>and</strong> they <strong>of</strong>fer fewer sorption sites for alcohol ethoxylates than<br />

the amorphous MX <strong>of</strong> Citrus <strong>and</strong> Prunus; for this reason, Kww are lower than Kmxw.<br />

A similar observation had been made with lipophilic solutes lacking surface actvity<br />

(Sect. 6.1) where Kww <strong>and</strong> Kcw are compared.<br />

These results are specific for barley <strong>and</strong> Chenopodium wax, <strong>and</strong> should not be<br />

extrapolated to waxes <strong>of</strong> other species. With Stephanotis wax, considerably higher<br />

Kww were observed (Table 7.1). Maximum concentrations (g kg −1 ) <strong>of</strong> alcohol<br />

ethoxylates sorbed in Citrus MX (7.9) are a function <strong>of</strong> Ey (Riederer <strong>and</strong> Schreiber<br />

1995), as was previously shown for wax [(7.4) <strong>and</strong> (7.5)].<br />

logC max<br />

wax = 2.07 − 0.044Ey<br />

(7.9)<br />

7.1.3 Sorption <strong>of</strong> n-Alkyl Esters in Wax<br />

N-alkyl esters, lacking surface activity are lipophilic <strong>and</strong> have very low water<br />

solubility. Therefore, 100g l −1 1,2-propanediol was added to water to obtain homogeneous<br />

aqueous solutions without phase separation (Simanova et al. 2005).<br />

Partitioning <strong>of</strong> n-alkyl esters between these external aqueous solutions containing<br />

1,2-propanediol <strong>and</strong> reconstituted wax was measured with Hordeum <strong>and</strong> Stephanotis<br />

wax. These partition coefficients are marked Kwrec (rec = receiver), instead <strong>of</strong> Kww.<br />

Identical solutions <strong>of</strong> n-alkyl esters containing 1,2-propanediol were also used as<br />

receiver solutions in transport experiments (Sect. 7.3.3).

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