Frying of Foods: Vassiliki Oreopoulou, Magdalini Krokida, and Dimitris Marinos-Kouris
Frying of Foods: Vassiliki Oreopoulou, Magdalini Krokida, and Dimitris Marinos-Kouris
Frying of Foods: Vassiliki Oreopoulou, Magdalini Krokida, and Dimitris Marinos-Kouris
CONTENTS
TABLE 52.1
The Main Classes of Fried Products
(Potato) Chips Potato chips of various shapes and flavors, tortilla chips, and corn chips 25–40
Extruded snacks Snacks of various shapes, flavors and texture, prepared with cereal, potato, or legume flour 20–40
Nuts Nuts or nut mixtures with legumes and flavorings 5–6a
Bakery products Doughnuts and fried pies 10–25
Par-fried frozen food French fries, fish, chicken, and pancakes 5–7
Food-service products Chicken, fish, meat, and potatoes Broad range
a
Exchanged with natural oil.
@2Q @Q @Q
Crust kII þ Nbx cpb ¼ («b rb cpb þ «s rs cps ) (52:3)
@x2 @x @t
In crust region
@Q @2Q @Q
(«g rg cpg þ «s rs cps ) ¼ kI 2 þ Ngx cpg (52:4)
@t @x @x
Oil
Metal
where kI, kII are the thermal conductivities in crust
Heat, Oil
and core regions, respectively (W m1 8C1), Q is the
temperature (8C), Nix is the flux of species i in x-
Moisture direction (kg m2 s1), cpi is the specific heat of spe-
(a) (b) cies i (J kg1 8C1), «i is the volume fraction of species
i (mi3mt3), ri is the density of species i (kg of i m3
i ),
FIGURE 52.1 Heat and mass transfer in: (a) shallow frying and subscripts b, g, and s refer to liquid water, water
and (b) deep-fat frying. vapor, and solid, respectively.
where m is the moisture content at time t, mo is the initial M 0 ¼ 62:9 0:189t (52:15)
moisture content, Kc and Ke, are the rate constants of O ¼ 7:87 0:0888t (52:16)
the mass lumped capacity of the core and the edge, pffiffi
respectively, and a is the fraction of the total water M 0 ¼ 100 5:34 t (52:17)
contained in the core of the raw material. pffiffi
Kozempel et al. [36], proposed the use of Fick’s O ¼ 9:70 2:53 t (52:18)
law (for an infinite slab) for the estimation of the
moisture content of fried french fries, which depends Krokida et al. [37] presented the following kinetic
on the diffusion of water vapor in the material model for water loss during frying of french fries:
X Xe
M 8 ¼ exp (KX t) (52:19)
¼ Xo Xe
Mo p2
2 2 1 2 2 1 2 2
where X is the potato moisture content (kg/kg db), in
e(Dp t=L ) þ e9(Dp t=L ) þ e25(Dp t=L ) þ
9 25 frying time t (min), Xo is the initial moisture content (kg/
(52:12) T KXT b KXd 1 C KXC
kg db), KX ¼ KoX 170 10 2 þ 100 is the rate
1
where M is the potato moisture, t is the residence time, constant of moisture content kinetics (min ), b is the
Mo is the initial moisture, L is the nominal thickness of sample size (mm), C is the concentration of hydrogen-
T XT b Xd 1 C XC
cut potato, and D ¼ Doe(E/RT) is the diffusion coef- ated oil in total oil (%), Xe ¼ Xoe 170 10 2 þ 100
ficient, which has to be calculated as a function of is the moisture content in equilibrium (kg/kg db), and
temperature due to rapid temperature change that the KoX, KXT, KXb, KXC, Xoe, XT, Xb, XC are parameters.
potato pieces undergo in the oil bath. It should be For the oil uptake they proposed the kinetic model,
noted that only the first term is significant.
They also develop the following equation for the Y ¼ Ye [1 exp (KY t)] (52:20)
estimation of oil absorption, assuming that it depends
on the moisture and texture of the potato pieces, where Y is the oil content of potato strips (kg/kg db),
T YT b Yd 1 C YC
Ye ¼ Yoe 170 10 2 þ 100 is the oil content at
dS (k1 TX ) T KYT
¼ ko e þ k2 (M) e(E=RT) (52:13) infinite process time (kg/kg db), KY ¼ KoY 170
dt b KYd 1 C KYC
10 2 þ 100 is the rate constant of oil uptake
where S is the concentration of oil (wt oil/wt potato), (min1), and Yoe, YT, Yb, YC, KoY, KYT, KYb, KYC are
t is the time (h), TX is the texture (N), ko is a parameters.
2.5
1.5 Tristearin
Cottonseed oil
Soybean oil
1
0 50 100 150 200 250
Temperature (⬚C)
FIGURE 52.2 Specific heat of common pure triglycerides and natural oils.
52.3.2 PHYSICAL AND CHEMICAL PROPERTIES physical properties of the oils, but also the sensorial
properties and nutritional value.
Fresh oils consist mainly (up to 98%) of triglycerides.
Characteristics permitting oil use for deep fat frying
52.3.2.1 Vapor Pressure
are high vapor pressure and resistance to decompos-
ition. Decomposition of oils during frying proceeds Vapor pressure, related to boiling point, is one of the
through thermal, oxidative, and hydrolytic reactions. most important characteristics for the application of
The first reactions result in the formation of various oils to frying processes. Triglycerides of long-chain
oxidized and polymerized products, while the latter in fatty acids have extremely low vapor pressure, which
free fatty acids, mono- and di-glycerides. All these increases as the fatty acid chain length decreases.
substances cause an alteration of not only the Vegetable oils, consisting mainly of triglycerides
with long-chain fatty acids, have consequently very
low vapor pressure, e.g., 0.001 and 0.05 mm Hg at
254 and 3088C, respectively, for soybean and olive
TABLE 52.3 oil [24].
Thermal Conductivities of Commercial Fatty Acids Monoglycerides have considerably higher vapor
pressures, and fatty acids are even more volatile.
Acid Temperature (8C) Thermal Conductivity (W/m 8C)
Therefore, these products of hydrolytic cleavage are
Lauric 72.5 0.192 a source of smoke arising from used frying oil. The
90 0.185 vapor pressures or boiling points of some saturated
106 0.174 fatty acids are given in Table 52.4 [24]. The logarithm
148 0.138 of vapor pressure of fatty acids and typical synthetic
Oleic 72.5 0.188 triglycerides is a linear function of the reciprocal of
90 0.178
the absolute temperature [24]. The heat of vaporiza-
106 0.155
tion of fatty materials has been calculated from vapor
148 0.115
Palmitic 72.5 0.172
pressure data by means of the Clausius-Clapeyron
90 0.157 equation and amounts to 238 kJ kg1 for oleic and
106 0.138 stearic acids at atmospheric pressure and 209 kJ kg1
148 0.102 for soybean oil at 0.001 to 0.05 mm Hg [24].
Steatic 72.5 0.160
90 0.146 52.3.2.2 Smoke, Fire, and Flash Points
106 0.132
148 0.096 The smoke, fire, and flash points of a fatty material
are measures of its thermal stability when heated in
contact with air. The smoke point is the temperature 52.3.2.4 Surface Tension
at which smoking is first detected in a laboratory
apparatus protected from drafts. The flash point is Fresh oils consist mainly of triglycerides and are im-
the temperature at which the volatile products are miscible with water, which is the main constituent of
evolved at a rate sufficient to be ignited, but not to all foods. The surface tension between oil and food
support combustion. The fire point is the temperature reduces by the action of polar compounds that are
at which the volatile products support continued formed through degradation reactions and leaching
combustion. of food materials into the oil during the frying pro-
Fatty acids are much more volatile than glycer- cess. As a result, oil and food contact increases and
ides; therefore, smoke, flash, and fire points of oils heat transfer becomes more effective. Blumenthal [5]
depend principally on the content of free fatty acids, observed that the contact time of fresh oil at the food
and decrease if hydrolytic degradation is extended surface is only about 10% of the food immersion time.
during frying. The smoke point of cottonseed, corn, As the oil continues to be used, the contact time
or peanut oils, e.g., decreases from about 2328C at a increases to about 20%, then optimally to about
free fatty acid content of 0.01% to 938C at a free fatty 50%. This causes normal absorption of oil into food
acid content of 100%. The unsaturation of oil has and proper cooking of the exterior and the interior.
hardly any effect on its smoke, flash, and fire points. If the oil degrades further, more surfactants are
formed, causing an increased contact time (80% or
52.3.2.3 Viscosity higher). As a result, an excessive oil pickup by the
food and an increased rate of heat transfer to the
The viscosity of an oil is strongly affected by the surface of the food is observed, while conduction of
degradation during frying, increasing as a result of heat to the interior cannot be sped up by changes in
the formation of dimers and polymers through ther- the oil. Thus, excessive darkening and drying at the
mal and oxidative degradation [5,11,55]. Keeping the surface occur.
oil at frying temperature caused an increase of viscos- Sodium oleate, a water-activated surfactant, was
ity with time, which was even higher when the oil was isolated from the polar fraction of frying fat [6,27].
aerated [12]. The increase observed during continuous Other water-activated surfactants are phospholipids
heating of the oil was higher than that during frying and inorganic salts. Lipid-activated surfactants in-
at the same temperature (27% compared with 11% clude low-polar thermal polymers and high-polar oxi-
after 90 h at 1858C [11]. Experiments of potato frying dated compounds. The mono- and di-glycerides
with corn oil showed that after 36 h of frying, when formed through hydrolysis also cause a rapid drop
smoking and foaming of the oil indicated that it was of the interfacial tension between oil and water [23].
no longer suitable for frying, its viscosity had in- The oil–air surface tension was found to decrease
creased by 28.6% [27]. by 2.20% after 36 h of potato frying [27]. At high
TABLE 52.5
Main Groups of Compounds Formed during Deep-Fat Frying