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Food Science and Technology International
DOI: 10.1177/1082013203009002006
2003; 9; 101 Food Science and Technology International
H. Dogan and M. V. Karwe
Physicochemical Properties of Quinoa Extrudates
http://fst.sagepub.com/cgi/content/abstract/9/2/101
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Physicochemical Properties of Quinoa Extrudates
H. Dog an
1
and M.V. Karwe
2,
*
1
TUBITAK Marmara Research Center, Food Science and Technology Research Institute,
P.O. Box 21, Gebze/Kocaeli, 41470, Turkey
2
Food Science Department, Rutgers University, 65 Dudley Road, New Brunswick, NJ, 08901 USA
Response surface methodology (RSM) was used to analyse the effect of temperature, screw speed, and
feed moisture content on physicochemical properties of quinoa extrudates. A three-level, three-variable,
Box-Behnken design of experiments was used. The experiments were run at 1624% feed moisture content,
130170
C temperature, and 250500 rpm screw speed with a fixed feed rate of 300 g/min. Second order
polynomials were used to model the extruder response and extrudate properties as a function of process
variables. Responses were most affected by changes in feed moisture content and temperature, and to a
lesser extent by screw speed. Calculated specific mechanical energy (SME) values ranged between 170
402 kJ/kg which were lower than those observed for other cereals, most likely due to high (7.2%) fat
content of quinoa. High levels of feed moisture alone, and in combination with high temperature, resulted
in poor expansion. The best product, characterised by maximum expansion, minimum density, high degree
of gelatinization and low water solubility index, was obtained at 16% feed moisture content, 130
C die
temperature, and 375 rpm screw speed, which corresponds to high SME input. It was demonstrated that
the pseudo-cereal quinoa can be used to make novel, healthy, extruded, snack-type food products.
Key Words: quinoa, extrusion cooking, physico-chemical properties
INTRODUCTION
Quinoa (Chenopodium quinoa Willd.) is a disc shaped
small seed that looks like a cross between sesame seed
and millet. It is a crop that has been grown in South
American countries for centuries and has many poten-
tially beneficial properties such as resistance to cold
(Becker and Hanners, 1990; Coulter and Lorenz, 1991a;
Prakash et al., 1993). It can be grown in poor soil and at
high altitude (Ng et al., 1994). The edible seed of the
quinoa plant has been called both a pseudo-cereal and a
pseudo-oilseed because of its unique nutritional profile.
It has been recently identified to have promising
potential to overcome worlds food shortage (Ahamed
et al., 1996). The seeds have protein quality comparable
to that of whole dry milk in terms of balanced amino
acid composition (Ng et al., 1994). Quinoa protein is
rich in lysine, methionine and cysteine (Becker and
Hanners, 1990). Thus, it is a good complement for
legumes, which are often low in methionine and
cysteine. Some types of wheat come close to matching
protein content of quinoa, but cereals such as corn and
rice generally have less than half the protein content of
quinoa. In addition, quinoa is a relatively good source
of vitamin E, and several of the B vitamins (Ruales and
Nair, 1993; Ahamed et al., 1996). It also has desirable
fatty acid composition, and high levels of calcium, iron
and phosphorous (Ruales and Nair, 1993; Przybylski
et al., 1994) which make it a unique food source.
The Aztecs and Incas credited quinoa with medicinal
properties including lowering blood cholesterol, improv-
ing glucose tolerance and reducing insulin requirements
(Guzman-Maldonado and Paredes-Lopez, 1998). In
recent years, scientific information supporting the
health benefits of quinoa has accumulated (Guzman-
Maldonado and Paredes-Lopez, 1998). Quinoa contains
significant amounts of flavonoids and phenolic acids,
and a number of structurally diverse saponins (Ridout
et al., 1991; Gee et al., 1993; Ng et al., 1994;
Masterbroek et al., 2000). Saponins can help lower
cholesterol blood levels, inhibit growth of cancer cells,
eliminate digestive toxins, and strengthen the immune
system (Arditi et al., 2000). Phenolic derivatives act as
natural antimicrobial agents. They have been proven to
be very good antioxidants, scavenging free radicals and
providing metal chelating activities. Polyphenols have
been implicated in health benefits, such as prevention of
cancer and cardiovascular diseases.
This unique added chemical composition makes
quinoa an ideal candidate to be further studied for
establishing it as a functional food. Processing of
traditional grains like quinoa into products that deliver
nutritive as well as physiologically active components
represents a major opportunity for food processors
catering to the health-food market.
Extensive studies on extrusion processing of cereals,
such as corn and wheat, to generate ready-to-eat
*To whom correspondence should be sent
(e-mail: karwe@aesop.rutgers.edu).
Received 11 July 2002; revised 18 December 2002.
Food Sci Tech Int 2003;9(2):010114
2003 Sage Publications
ISSN: 1082-0132
DOI: 10.1177/108201303033940
101
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breakfast cereals and snacks, have been carried out
(Chinnaswamy and Hanna, 1990; Case et al., 1992; Cai
and Diosady, 1993; Guha et al., 1997). The only study
reported in literature on extrusion of quinoa (Coulter
and Lorenz, 1991a, b) is about the nutritional, sensory
and physical characteristics of quinoa-corn grit blends
(up to 30 : 70 ratio) extruded at 1525% feed moisture
content, 100150
C), and
screw speed (250500 rpm). A three-variable, three-
level, Box-Behnken design (Table 2) was employed to
determine the extrusion conditions. Experiments were
randomized in order to minimize the systematic bias in
the observed responses due to extraneous factors.
Preparation of Samples
Samples were collected under steady state conditions
of pressure, torque and temperature. Immediately after
extrusion, extrudates were cooled, packed into glass jars,
flushed with nitrogen gas, sealed and kept refrigerated
(5
C) until analysis.
Process Responses
The ZSK-30 extruder is equipped with a torque
indicator which shows % torque which is proportional
to the current drawn by the drive motor. A reading
of 100% torque corresponds to the max allowable
torque of 172 Nm. The specific mechanical energy
(SME) was calculated from the measured torque reading
as follows (Godavarti and Karwe, 1997):
SME kJ=kg
Total torque (%) Friction torque (%) N9:1
100 500m
f
1
The drive motor has a rated power of 9.1 kW at a
rated screw speed of 500 rpm. The friction torque was
measured with screws attached to the drive and the
barrel empty.
The determination of specific energy delivered
(SED) to the extrudate is based on the energy balance
(Figure 1) between the inlet and just before the exit at
the die of the extruder under steady state conditions
computed from the following equations,
m
f
C
p
i
T
i
Q
H
Q
C
ME m
f
C
p
o
T
p
2
Q
H
Q
C
m
f
ME
m
f
C
p
o
T
p
C
p
i
T
i
3
SME and SED were measured from experimental
conditions and STE was calculated from Equation (4).
STE SME SED 4
Negative value of specific thermal energy (STE)
indicates net cooling at the barrel.
Product Responses
Extrudate samples used for determination of the
degree of gelatinization (DG), water solubility index
(WSI), and water absorption index (WAI), were dried at
45
C) S (rpm)
1 1 0 24 170 375
1 1 0 24 130 375
1 1 0 16 170 375
1 1 0 16 130 375
0 1 1 20 170 500
0 1 1 20 170 250
0 1 1 20 130 500
0 1 1 20 130 250
1 0 1 24 150 500
1 0 1 24 150 250
1 0 1 16 150 500
1 0 1 16 150 250
0 0 0 20 150 375
0 0 0 20 150 375
0 0 0 20 150 375
Figure 1. Schematic diagram showing the barrel of
extruder and various energy flows.
Quinoa Extrudates 103
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some modifications. WSI was calculated as follows:
WSI
g water soluble matter
g dry sample
5
For the calculation of WAI the total solids in the
original sample were corrected for the loss of solubles in
the supernatant and WAI was expressed as,
WAI
g water absorbed
g dry sample 1 soluble fraction
6
Product density (
e
) was measured by volumetric
displacement method as described by Hic s as maz and
Clayton (1993). Glass beads of 0.5 mm diameter
(Biospec Products, Inc., Bartlesville, OK) were used as
displacement medium. Density of glass beads was
determined as 1550 kg/m
3
, then the density of extrudates
was calculated as
e
W
e
W
gb
gb
7
The
e
values were obtained from five random
samples for each extrusion condition, with three
replications.
The sectional expansion index (SEI) of extrudate was
measured as the ratio of the diameter of the extrudate to
that of the die. The extrudate diameter was measured
with a digital Vernier caliper and the results were
expressed as the average of hundred measurements on
each condition. The longitudinal (LEI) and volumetric
expansion (VEI) indices were calculated according to
Alvarez-Martinez et al. (1988).
Textural properties of extrudates were measured using
TA-XT2 texture analyser (Stable Micro Systems, UK).
A three-point bend rig with a support length (bridge) of
30 mm and a rounded plate probe (15 mm5 mm,
D5 mm) exerting force in the middle of bridge were
used to test extrudates in the bend mode (Zasypkin and
Lee, 1998). The test speed was 2 mm/s and the full load
scale was 50 kg. Data were processed with an XT-RA
Dimension software package (Stable Micro Systems,
Haslemere, Surrey, UK). The hardness of dry extrudates
was measured as the peak force offered by the sample
during cutting. Breaking strength (N/mm
2
) was calcu-
lated as the peak breaking force (N) divided by the
cross-sectional area (mm
2
) calculated for each extrudate
sample. The reported values are the averages of 15
measurements.
The color of ground unprocessed quinoa and
extrudate samples was measured in triplicate using
Minolta Chroma Meter (CR-210) in terms of Hunter
Lab values (L, a, b), where L represents lightness with 0
for dark and 100 for bright, a represents the extent of
green colour in the range from 100 to 0 and red in the
range 0 to 100, b quantifies blue colour in the range
from 100 to 0 and yellow in the range from 0 to 100.
The total colour change (E) was then calculated as
E
L
2
a
2
b
2
q
8
where LL L
0,
ia a a
0
, and b b b
0
; the
subscript
0
indicates initial colour values before
processing.
Analysis of Data
Process responses (SME, SED, STE, SME/SED) and
product responses (iE,
e
, WAI, WSI, DG, SEI, LEI,
VEI, hardness and breaking strength) obtained as a
result of the proposed experimental design were
subjected to regression analysis in order to assess the
effects of feed moisture content, extrusion temperature
and screw speed. Second-order polynomials of the form
y
i
b
0
X
3
i1
b
i
X
i
X
3
i1
X
3
ji
b
ij
X
i
X
j
9
were fitted to the independent variables and were
computed by using SAS (version 8.1) statistical package,
where X
i
, X
i
X
i
and X
i
X
j
are linear, quadratic, and
interaction effect of the input variables which influence
the response y, respectively, and b
0
, b
i
, and b
ij
are the
model constants to be determined. All crosscorrelations
between the process and product responses themselves
were also assessed. The response surface plots for these
models were plotted as a function of two variables, while
keeping the third variable constant at its intermediate
value.
RESULTS AND DISCUSSION
Composition of grain could vary with variety and
growing conditions, even though experimental results for
composition (Table 3) agreed with previous data (Becker
and Hanners, 1990; Coulter and Lorenz, 1990; Guzman-
Maldano and Paredes-Lopez, 1998; Koziol, 1992;
Prakash et al., 1993; Ruales and Nair, 1993). The
quinoa seeds used in this study have high crude protein,
crude fat and ash than common cereals, such as rice and
corn. Extrudates of widely different physical structure
were obtained by twin-screw extrusion of quinoa flour at
different combinationsofprocessingparameters(Table2).
Regression analyses of the physicochemical properties of
quinoa extrudates (Table 4) indicated that all the second
104 H. DOG
C die
temperature and 500 rpm screw speed (SME386 kJ/
kg, SME/SED1.85). The linear effects of temperature
Table 3. Proximate composition and some properties
of unprocessed quinoa flour.
Quinoa Flour Characteristics
Proximate composition (g/100g) MeanSD (n3)
Moisture 10.960.06
Protein 11.950.12
Lipid 7.190.02
Ash 2.150.02
CHOfiber 67.75
Colour
L 87.270.30
a 0.480.03
b 11.940.41
Water absorption index (g H
2
O/g dry sample) 1.690.11
Water solubility index (g water soluble
matter/g dry sample)
0.0730.003
Amylose content (%) 11.10.04
Quinoa Extrudates 105
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Table 4. Results of regression analysis (calculated on coded levels where all independent variables are in the range 1).
Levels
Degree of
Geltn
Density
(kg/m
3
)
Sectional
Expansion
Index
Longitudinal
Expansion
Index
Volumetric
Expansion
Index
Water
Solubility
Index
(g/g)
Water
Absorption
Index
(g/g) iE
Hardness
(N)
Breaking
Strength
(N/mm
2
)
Specific
Mechanical
Energy
(kJ/kg)
Specific
Energy
Delivered
(kJ/kg)
Specific
Thermal
Energy
(kJ/kg) SME/SED
C 0.781*** 246.7*** 2.75*** 0.630** 4.78*** 0.202*** 6.03*** 21.35*** 3.62*** 0.068*** 258.0*** 260.8*** 2.9
ns
0.989***
M 0.046*** 88.1*** 0.43*** 0.090
ns
1.67*** 0.025*** 0.57*** 1.88*** 0.19
ns
0.041*** 37.9*** 13.8*** 51.9*** 0.206***
T 0.058*** 30.4*** 0.73*** 0.650*** 0.99** 0.017*** 0.14** 0.84** 1.04*** 0.028*** 59.3*** 40.8*** 100.1*** 0.407***
S 0.034*** 38.0*** 0.15* 0.010
ns
0.61
ns
0.021*** 0.20*** 0.53
ns
0.17
ns
0.016** 51.3*** 0.0
ns
51.0*** 0.203***
MM 0.033** 57.9*** 0.24** 0.296
ns
0.33
ns
0.026*** 0.33*** 1.49** 0.46* 0.017* 15.6* 0.1
ns
24.1
ns
0.041
ns
T T 0.037*** 34.6** 0.39*** 0.711** 0.96
ns
0.031*** 0.15* 2.67*** 0.62** 0.021** 23.8** 0.1
ns
24.1* 0.155***
SS 0.041*** 38.2** 0.04
ns
0.364
ns
0.77
ns
0.009** 0.19** 0.25
ns
0.34
ns
0.001
ns
9.8
ns
0.1
ns
9.8
ns
0.031
ns
MT 0.015
ns
4.0
ns
0.17
ns
0.218
ns
0.92
ns
0.002
ns
0.53*** 0.10
ns
0.07
ns
0.017* 11.6
ns
2.2*** 9.8
ns
0.092**
MS 0.015
ns
18.8
ns
0.10
ns
0.038
ns
0.05
ns
0.003
ns
0.02
ns
0.76
ns
0.32
ns
0.006
ns
9.0
ns
0.0
ns
9.0
ns
0.044
ns
T S 0.009
ns
26.8** 0.02
ns
0.098
ns
0.66
ns
0.011** 0.06
ns
0.10
ns
0.15
ns
0.004
ns
7.9
ns
0.0
ns
8.0
ns
0.066
ns
R
2
0.98 0.98 0.98 0.90 0.89 0.99 0.98 0.96 0.94 0.97 0.97 1.00 0.99 0.99
F 28.28 28.68 24.65 5.25 4.59 102.6 27.13 13.97 9.48 16.14 21.06 infty 43.22 52.85
Sig. F 0.001 0.001 0.001 0.041 0.052 0.000 0.001 0.005 0.012 0.003 0.002 0.000 0.000 0.000
C: model constant; M, T and S: linear effects of moisture content, die temperature and screw speed, respectively. MM, T T and SS: quadratic effects of moisture content, die temperature and screw speed,
respectively;. MT, MS and T S: interaction effects of moisture content and die temperature, moisture content and screw speed, and die temperature and screw speed, respectively; ***significant at p<0.01,
**significant at p<0.05, *significant at p<0.10,
ns
non-significant at p0.10.
1
0
6
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.
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.
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.
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(T), screw speed (S) and moisture (M), and the
quadratic effects of screw speed (SS) and tempera-
ture (TT) had the highest impact, significant at
p<0.01, on the DG (Table 4). During extrusion cooking
both temperature and shear are responsible for starch
gelatinization (Della Valle et al., 1989; Kokini, 1993).
Although at high screw speeds the residence time is low,
an increase in screw speed increased the DG signifi-
cantly ( p<0.01) for all combinations of feed moisture
content and temperature (Figure 3). This confirmed that
shear is a significant contributor to starch gelatinization.
This was supported by stronger effect of moisture on
DG at lower temperatures. These results agreed with
those of Gomez and Aguilera (1984), Bhattacharya and
Hanna (1987) and Cai and Diosady (1993) for other
grains.
Figure 3. Effect of feed moisture content, die tem-
perature and screw speed (rpm) on the degree of
gelatinization (DG).
Table 5. Cross-correlation coefficients between product and process responses.
DG PD SEI LEI VEI WSI WAI iE H BS SME SED STE SME/SED
DG 1 0.60 ** 0.91*** 0.75*** 0.57** 0.19
ns
0.14
ns
0.33
ns
0.60** 0.85*** 0.81*** 0.73*** 0.83*** 0.79***
PD 1 0.62** 0.17
ns
0.89*** 0.66*** 0.46* 0.24
ns
0.05
ns
0.78*** 0.74*** 0.48* 0.70*** 0.70***
SEI 1 0.80*** 0.65*** 0.02
ns
0.26
ns
0.27
ns
0.72*** 0.85*** 0.78*** 0.88*** 0.86*** 0.83***
LEI 1 0.16
ns
0.33
ns
0.05
ns
0.33
ns
0.90*** 0.64*** 0.46* 0.69*** 0.57** 0.49*
VEI 1 0.47* 0.41
ns
0.04
ns
0.09
ns
0.68*** 0.77*** 0.58** 0.75*** 0.79***
WSI 1 0.10
ns
0.15
ns
0.48* 0.03
ns
0.39
ns
0.18
ns
0.22
ns
0.24
ns
WAI 1 0.23
ns
0.09
ns
0.53** 0.18
ns
0.41
ns
0.27
ns
0.25
ns
E 1 0.06
ns
0.43
ns
0.11
ns
0.08
ns
0.11
ns
0.17
ns
H 1 0.42
ns
0.37
ns
0.72*** 0.51* 0.47*
BS 1 0.73*** 0.70*** 0.76*** 0.71***
SME 1 0.74*** 0.97*** 0.97***
SED 1 0.88*** 0.86***
STE 1 0.99***
SME/SED 1
DG: degree of gelatinization; PD: product density; SEI: sectional expansion index; LEI: longitudinal expansion index; VEI: volumetric expansion index; WSI: water
solubility index; WAI: water absorption index; iE: total color change; H: hardness; BS: breaking strength; SME: specific mechanical energy, SED: Specific energy
delivered; STE: specific thermal energy; ***significant at p<0.01, **significant at p<0.05, *significant at p<0.10,
ns
non-significant at p0.10.
Figure 2. Variation of degree of gelatinization (DG)
with SME/SED.
Quinoa Extrudates 107
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In general, low feed moisture and high product
temperature have been found to increase the DG in
extrusion of starchy materials (Bhattacharya and
Hanna, 1987; Cai and Diosady, 1993). However, in the
presence of lipids, extrusion temperature required for
maximum DG was in the intermediate range. Lower
temperatures compensated for the decrease in melt
viscosity due to lipids (Dog an, 2000). In high lipid
containing cereals like quinoa, excessive feed moisture
acts as a secondary lubricant which prevents the
achievement of appropriate development or cooking of
dough by shear induced disruption. In this study, DG
was found to be highly correlated (0.81, p<0.01) with
SME, which confirmed that quinoa flour needs high
shear environment for effective extrusion processing.
Density of Extrudates,
e
The density of dry extrudates varied between 117 and
507 kg/m
3
. Low density, which is a desirable character-
istic of the expanded product, was achieved with low
feed moisture content, low temperature, and high screw
speed combination. The response surface (Figure 4)
shows that feed moisture content had a dominant effect
on density followed by screw speed, whereas tempera-
ture seems to have a minor effect. Minimal product
density was obtained at feed moisture of 17.1%, 161
C
die temperature, and 392 rpm screw speed.
Expansion Indices
The measured SEI of quinoa extrudates ranged from
0.92 to 3.58 whereas LEI ranged from 0.50 to 2.95
(Table 4). SEI was significantly affected by temperature,
feed moisture content and screw speed while for LEI
both feed moisture content and screw speed were found
to be insignificant. High expansion ratio at low feed
moisture content for extruded products is typical for
cereals (Coulter and Lorenz, 1991b; Faubion and
Hoseney, 1982; Gomez and Aguilera, 1984).
Moreover, Singh and Smith (1997) reported a decrease
in expansion with increasing temperature and feed
moisture content for wheat starch, wheat meal, and
oat flour. At higher moisture content, further decrease
in viscosity by increase in temperature results in a
reduced sectional expansion. At high feed moisture
content SEI increased with increasing screw speed while
at low moisture content levels effect of screw speed was
not significant (Figure 5). The positive effect of die
temperature on LEI (Figure 6) indicated the strong
dependency of elongation on extensional viscosity,
which decreases with increase in temperature, as
reported by Alvarez-Martinez et al. (1988). This is also
evident by the high negative correlation (0.75,
p<0.01) between DG and LEI (Table 5). Expansion
phenomena have been known to be basically dependent
on viscous and elastic properties of melted dough
(Launay and Lisch, 1983). Viscosity of feed melt
increases with an increase in DG (Bhattacharya and
Choudhury, 1994), therefore, LEI decreases.
It has been reported that the dough elasticity forces
contribute to radial expansion and axial contraction
(Padmanabhan and Bhattacharya, 1989). This relation
was also apparent in our experimental results with a
high negative correlation between SEI and LEI of 0.80
( p<0.01). Starch gelatinization is the functional prop-
erty that is directly related with physical properties of
the extruded products (Ghiasi et al., 1983). In the
present study, DG was found to be highly correlated
with SEI (0.91, p<0.01). As a measure of the extent of
molecular transformations during extrusion cooking
SME also correlated well with SEI (0.78, p<0.01).
Launay and Lisch (1983) suggested that the sectional
expansion and longitudinal expansion were dependent
on melt elasticity and melt viscosity, respectively. SEI
Figure 4. Effect of feed moisture content, die tem-
perature and screw speed on product density.
108 H. DOG
C die tempera-
ture, 19.1% feed moisture, and 425 rpm screw speed.
The mechanical properties of extruded products can
be described either by compressive deformation or by
breaking strength (Colonna et al., 1989). Breaking
strength is the measure of the strength of cell wall
which is expected to affect the texture and sensory
crispiness of the extruded product (Chen et al., 1991).
Breaking strength was found to be highly correlated
with SEI (0.85, p<0.01), indicating that the increase in
pore size together with a decrease in cell wall thickness
results in weak extrudate structures (Table 5). Generally,
breaking strengths of extrudates reflect expansion
volume (Chavez-Jauregui et al., 2000). High density
product naturally offers high breaking strength evident
by high correlation between product density and break-
ing strength (0.78, p<0.01 ). Chemical changes taking
place during extrusion cooking influence the develop-
ment of textural and mechanical properties such as
hardness and breaking strength in extrudates. Breaking
strength is affected by the strength of cell walls, as
influenced by starch gelatinization and protein dena-
turation (Martinez-Serna and Villota, 1992). The high
correlation found between DG and hardness (0.60,
p<0.05) and DG and breaking strength (0.85,
p<0.01) supports this relation.
Water Solubility and Absorption Indices
Water solubility index is related to the quantity of
soluble solids, which is related to dextrinization. The
coefficient of determination for WSI was highly
significant as revealed by a high value of R
2
(0.99).
The linear and quadratic effects of feed moisture (M)
content, linear effect of screw speed (S), and the linear
(T) and quadratic (TT) effects of temperature had
significant effect on WSI. In general ,WSI increased with
increasing temperature and screw speed and decreasing
Figure 7. Effect of feed moisture content, die tem-
perature and screw speed on product hardness.
Figure 8. Effect of feed moisture content, die tem-
perature and screw speed on breaking strength.
110 H. DOG
C)
T
o
outlet temperature of the product (
C)
T
d
die temperature or product temperature (
C)
VEI volumetric expansion index (dimensionless)
WAI water absorption index (g water absorbed/g dry
sample)
W
e
weight of extrudate (kg)
W
gb
weight of glass beads displaced by the extru-
dates (kg)
WSI water solubility index (g water soluble matter/g
dry sample)
E total colour change
e
density of extrudate (kg/m
3
)
gb
density of glass beads (kg/m
3
)
ACKNOWLEDGEMENTS
This is publication No. D 01544-01-01 of the New
Jersey Agricultural Experiment Station supported by
State funds and the Center for Advanced Food
Technology (CAFT). The Center for Advanced Food
Technology is a New Jersey Commission on Science
and Technology Center. Author H. Dog an acknowl-
edges the financial support from TUBITAK Marmara
Research Center, Food Science and Technology Res-
earch Institute, Turkey.
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114 H. DOG