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Lynne Wong's PhD thesis

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Stalk fibre Stalk pith Rind fibre<br />

10 0<br />

10 0<br />

10 0<br />

qst /kJ mol -1<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

- 6 0<br />

- 6 0<br />

- 6 0<br />

Rind fines Top fibre Dry leaf fibre<br />

10 0<br />

10 0<br />

10 0<br />

qst /kJ mol -1<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

- 6 0<br />

- 6 0<br />

- 6 0<br />

Dry leaf fines Green leaf fibre Green leaf fines<br />

10 0<br />

10 0<br />

10 0<br />

qst /kJ mol -1<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

6 0<br />

2 0<br />

- 2 0<br />

0 10 2 0 3 0 4 0<br />

- 6 0<br />

- 6 0<br />

- 6 0<br />

EMC/% db<br />

52 weeks<br />

36 weeks<br />

Figure 6.6. The variation of the net isosteric heat of adsorption calculated from the<br />

Hailwood-Horrobin model with moisture content for the nine cane components of<br />

R 570 aged 52 and 36 weeks.<br />

252

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