Lynne Wong's PhD thesis
Lynne Wong's PhD thesis Lynne Wong's PhD thesis
CHAPTER 5. ADSORPTION ISOTHERMS OF SUGAR CANE FIBRES In the previous chapter the Brix-free water content of the cane components are determined by means of a contact method. This chapter describes the experiments performed to determine the equilibrium moisture content, and hence adsorption properties, by means of a vapour sorption method of these cane component parts which enabled the determination of a number of thermodynamic parameters that provide insight into the microstructure of the fibre-water interface. 5.1 THE CONCEPT OF BOUND WATER IN FIBRE All biological systems have the ability to retain molecular hydration as a fundamental defensive mechanism against dehydration (Quioco et al., 1989). The structure, mobility and function of biological molecules are affected by the water molecules bound to the ionic, polar and hydrophilic sites of macromolecules (Vertucci and Leopold, 1987). Rascio et al. (1992) demonstrated the important role played by bound water in the plant's adaptation to the moderate stress of dehydration and related its tolerance towards dehydration to the quantity of bound water, the strength of binding and its ability to tolerate the removal of bound water without damage. However, the relationship between the quantity of bound water and water binding strength of plant tissues was not elucidated. In their review of moisture sorption isotherm characteristics of food products, Al-Muhtaseb et al. (2002) quoted that food preservation consisted of controlling the moisture content during the processing of foods, achieved either by removing it or binding it such that the food becomes stable to both microbial and chemical deterioration (Labuza, 1980). Later, the concept of water activity was introduced to indicate the ‘quality’ of the water content of food. It describes the degree of ‘boundness’ of water and hence, its availability to participate in physical, chemical and microbiological reactions. In a biological system, three aspects of water can be distinguished (Rizvi and Benato, 1984): 1) Structural, the position and orientation of water molecules in relation to each other and to macromolecules. 2) Dynamic, molecular motions of water molecules and their contribution to the hydrodynamic properties of the system.
3) Thermodynamic, water in equilibrium with its surroundings, at a certain relative humidity and temperature. Moreover, in a biological system, water is believed to exist with either unhindered or hindered mobility, referred to as free or bound water respectively. ‘Bound water’ is considered as that portion of water held in the material which exhibits physical properties significantly different from those of free water or bulk water (Berlin, 1981), through stronger hydrogen bonding than liquid water. Some of the characteristics of bound water are lower vapour pressure, high binding energy as measured during dehydration, reduced mobility, unfreezability at low temperature and unavailability as a solvent such as in the definition of Brix-free water (Labuza and Busk, 1979). Although each of these characteristics has been used to define bound water, each gives a different value for the amount of water which is bound. As a result of this, as well as the complexities and interactions of the binding forces involved, no universal definition of bound water has been adopted. 5.2 TYPES OF ADSORPTION AND ADSORPTION ISOTHERMS In this study the interaction of sugar cane fibres with water was studied. When a solid surface (in this case the sugar cane fibre) is exposed to a fluid (i.e. gas or liquid, and in this case water) adsorption occurs. It is understood to mean the increase in the density of the fluid in the vicinity of an interface. With certain systems, e.g. some metals exposed to hydrogen, oxygen or water, the adsorption process is accompanied by absorption, i.e. the penetration of the fluid into the solid phase. In such a case the term sorption is used and, in particular, when the adsorption and absorption processes cannot be distinguished experimentally. Distinction was made in the early 1930s between physical adsorption (physisorption) in which weak Van der Waals interactions are involved and chemical adsorption (chemisorption) in which the adsorbed molecules are attached by strong chemical bonding. The characteristic features distinguishing between the two types of adsorption may be summarised as follows: (a) Physisorption is a general phenomenon with a relatively low degree of specificity, whereas chemisorption is dependent on the reactivity of the adsorbent (solid 170
- Page 171 and 172: instead of 150 g of 10° Brix sucro
- Page 173 and 174: Table 4.2. Determination of Brix-fr
- Page 175 and 176: Table 4.3. Comparison of Brix-free
- Page 177 and 178: Table 4.4. Results of the determina
- Page 179 and 180: In order to test for homogeneity of
- Page 181 and 182: Table 4.7. Results of the repeat de
- Page 183 and 184: The experiment was repeated with th
- Page 185 and 186: e any residual moisture in the samp
- Page 187 and 188: By means of the same technique, Won
- Page 189 and 190: was still hot. Since the filter was
- Page 191 and 192: value determined could be corrected
- Page 193 and 194: Qin and White’s finding was confi
- Page 195 and 196: A sample size of 3.5 g with 75 g co
- Page 197 and 198: Figure 4.4. Fibre samples drying in
- Page 199 and 200: - One large fibre sample (rind) of
- Page 201 and 202: Table 4.18. Brix-free water values/
- Page 203 and 204: Table 4.20. Brix-free water values/
- Page 205 and 206: 4.7.3 Statistical analysis It is es
- Page 207 and 208: Table 4.23. Analysis of variance (B
- Page 209 and 210: pointing out that at 52 weeks old,
- Page 211 and 212: The crop of R 570 sampled in 2001 w
- Page 213 and 214: 4.7.4. Estimated Brix-free water co
- Page 215 and 216: The main difference in the two sets
- Page 217 and 218: Table 4.27. Predicted Brix-free wat
- Page 219 and 220: 4.8 SUMMARY AND CONCLUSIONS An anal
- Page 221: component parts, and verify the Bri
- Page 225 and 226: Langmuir (1916, 1917, 1918) propose
- Page 227 and 228: to determine the moisture sorption
- Page 229 and 230: Table 5.1. Some commonly used isoth
- Page 231 and 232: Lomauro et al. (1985) found that wi
- Page 233 and 234: and on agricultural products such a
- Page 235 and 236: Bruijn (1963) studied the mass incr
- Page 237 and 238: After measuring the EMC of dry corn
- Page 239 and 240: approached, that is, either by adso
- Page 241 and 242: Table 5.4. Water activity (a w ) of
- Page 243 and 244: 5.6.3 Procedure to determine equili
- Page 245 and 246: 5.6.4 Results and discussion An exa
- Page 247 and 248: Table 5.8. Equilibrium moisture con
- Page 249 and 250: Table 5.10. Equilibrium moisture co
- Page 251 and 252: Table 5.12. Equilibrium moisture co
- Page 253 and 254: 30 o C 45 o C 55 o C 60 o C Water w
- Page 255 and 256: m/m of 96% activity, a w (g/100g dr
- Page 257 and 258: vaporisation generally decreases fr
- Page 259 and 260: 30 o C isotherm 45 o C isotherm 55
- Page 261 and 262: 4 0 Stalk fibre 5 0 Stalk pith 5 0
- Page 263 and 264: 5.6.4.4 Fitting of sorption models
- Page 265 and 266: Table 5.19. Parameters of the sorpt
- Page 267 and 268: Table 5.21. Parameters of the sorpt
- Page 269 and 270: Table 5.23. Parameters of the sorpt
- Page 271 and 272: Table 5.25. Parameters of the sorpt
CHAPTER 5. ADSORPTION ISOTHERMS OF SUGAR CANE FIBRES<br />
In the previous chapter the Brix-free water content of the cane components are determined<br />
by means of a contact method. This chapter describes the experiments performed to<br />
determine the equilibrium moisture content, and hence adsorption properties, by means of<br />
a vapour sorption method of these cane component parts which enabled the determination<br />
of a number of thermodynamic parameters that provide insight into the microstructure of<br />
the fibre-water interface.<br />
5.1 THE CONCEPT OF BOUND WATER IN FIBRE<br />
All biological systems have the ability to retain molecular hydration as a fundamental<br />
defensive mechanism against dehydration (Quioco et al., 1989). The structure, mobility<br />
and function of biological molecules are affected by the water molecules bound to the<br />
ionic, polar and hydrophilic sites of macromolecules (Vertucci and Leopold, 1987).<br />
Rascio et al. (1992) demonstrated the important role played by bound water in the plant's<br />
adaptation to the moderate stress of dehydration and related its tolerance towards<br />
dehydration to the quantity of bound water, the strength of binding and its ability to<br />
tolerate the removal of bound water without damage. However, the relationship between<br />
the quantity of bound water and water binding strength of plant tissues was not elucidated.<br />
In their review of moisture sorption isotherm characteristics of food products, Al-Muhtaseb<br />
et al. (2002) quoted that food preservation consisted of controlling the moisture content<br />
during the processing of foods, achieved either by removing it or binding it such that the<br />
food becomes stable to both microbial and chemical deterioration (Labuza, 1980). Later,<br />
the concept of water activity was introduced to indicate the ‘quality’ of the water content<br />
of food. It describes the degree of ‘boundness’ of water and hence, its availability to<br />
participate in physical, chemical and microbiological reactions. In a biological system,<br />
three aspects of water can be distinguished (Rizvi and Benato, 1984):<br />
1) Structural, the position and orientation of water molecules in relation to each<br />
other and to macromolecules.<br />
2) Dynamic, molecular motions of water molecules and their contribution to the<br />
hydrodynamic properties of the system.