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W. Richard Bowen and Nidal Hilal 4

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112 4. INvEsTIgATINg MEMbRANEs ANd MEMbRANE PROCEssEs<br />

–3<br />

1000 1200 1400 1600 1800 2000<br />

Piezo displacement [nm]<br />

should be avoided. As an example, Figure 4.5 shows a polystyrene colloid<br />

probe <strong>and</strong> data for the retraction of such a probe after it has been<br />

pushed into contact with membrane surfaces [3].<br />

The depths of the depressions of the curves in Figure 4.5 give direct<br />

quantification of the adhesion of the probes to the surfaces. The ES404<br />

membrane was an existing commercial membrane <strong>and</strong> the XP117 membrane<br />

is a development membrane designed to have lower fouling properties<br />

(both membranes are PCI Membranes). The development membrane<br />

had significantly lower adhesion <strong>and</strong> hence significantly lower fouling<br />

potential than the existing membrane.<br />

Ultrafiltration membranes are used particularly for the processing of<br />

solutions of biological macromolecules. Such molecules are too small to<br />

immobilise singly on a cantilever. However, by adsorbing such molecules<br />

onto colloid probes, it is possible to measure their adhesion to membrane<br />

surfaces. Such a protein (BSA – bovine serum albumin)-modified probe<br />

<strong>and</strong> the corresponding adhesion data for two membranes is shown in<br />

Figure 4.6 [4].<br />

The data shows that the protein-modified probe has significantly<br />

lower adhesion to the development membrane, XP117, than to the existing<br />

commercial membrane, ES404, <strong>and</strong> hence the modified membrane<br />

has significantly lower fouling potential in the processing of such protein<br />

solutions.<br />

Membranes are frequently used to process biological cell dispersions.<br />

In order to elucidate such processes, it has been proved possible<br />

to immobilise single cells at tipless AFM cantilevers, creating cell probes,<br />

whilst maintaining the viability of such a cell, Figure 4.7 [5].<br />

Such cell probes allow the direct measurement of the adhesion of biological<br />

cells to membranes. Interpretation of the data for such cell probes<br />

F/R [mN/m]<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

–1<br />

–2<br />

ES 404<br />

XP 117<br />

FIgURE 4.5 SEM image of a 11 �m polystyrene sphere attached to a tipless AFM cantilever<br />

<strong>and</strong> force versus piezo displacement plot (retraction) for two membranes in 10 �2 M<br />

NaCl solution at pH 8.0 (ES404, conventional; XP117, modified).<br />

D<br />

C<br />

B<br />

A'<br />

A

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