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Title
The Application of Freeze-Chill Technology to Ready-To-Eat Meal Components
Authors(s)
Redmond, G.A.; Dempsey, A.; Oxley, E.; et al.
Publication date
2002
Conference details
2002 ASAE Annual International Meeting/ CIGR XVth World Congress, Chicago, Illinois,
USA, 28-31 July 2002
Publisher
The Society for engineering in agricultural, food and biological systems
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Paper Number: 026185
An ASAE Meeting Presentation
The Application of Freeze-Chill Technology to ReadyTo-Eat Meal Components
G.A. Redmond, Dr.
(_
Teagasc, The National Food Centre, Castleknock, Dublin 15, Ireland.
Email: gredmond@nfc.teagasc.ie
A. Dempsey, Mr.
Department of Agricultural and Food Engineering, University College Dublin, Earlsfort Tee.,
Dublin 2, Ireland.
E. Oxley, Mr.
Department of Agricultural and Food Engineering, University College Dublin, Earlsfort Tee.,
Dublin 2, Ireland.
T.R. Gormley, Dr.
(·
\
Teagasc, The National Food Centre, Castleknock, DubHn 15, Ireland.
.
F. Butler, Dr.
Department of Agricultural and Food-Engineering, Universify-College Dublin, Earlsfo·rt Tee.,
Dublin 2, Ireland.
Email: f.butler@ucd.ie
The authors are solely responsible for the content of this technical presentation. The technical presentation does not necessarily
reflect the official position of the American Society of Agriculh.ual Engineers (ASAE), and its printing and distribution does not
constitute an endorsement of views which may be expressed. Technical presentations are not subject to the formal peer review
process by ASAE editorial committees; therefore, they are not to be presented as refereed publications. Citation of this work should
state that it is from an ASAE meeting paper. EXAMPLE: Author's Last Name, lnitiaJs. 2002. Trtle of Presentation. ASAE Meeting
Paper No. 02xxxx. St. Joseph, Mfch.: ASAE. For information about securing permission to reprint or reproduce a technical
presentation. please contact ASAE at hq@asae.org or 616-429-0300 (2950 Niles Road, St. Joseph, Ml 49085-9659 USA)~
Written for presentation
at the
2002 ASAE Annual International Meeting I CIGR XVth World Congress
Sponsored by ASAE and CIGR
Hyatt Regency Chicago
Chicago, Illinois, USA
July 28-July 31, 2002
Abstract. Freeze-chilfing involves freezing and frozen storage followed by thawing and chilled
storage. A number of ready-to-eat meal components have been studied for their suitability for freezechilling including, potatoes, carrots, green beans, broccoli, salmon and white sauces. In general,
sensory analysis showed that freeze-chilled products were similar in quality to their chilled or frozen
countetparls. There were some differences between the freeze-chilled and chilled products in
instrumental texture assessment and centrifugal drip loss due to cell damage arising from the
freezing step. A freezing rate study was carried out to detennine if more rapid freezing could improve
texture and drip. Mashed potato was frozen at -30, -60 or -90"C to an internal temperature of -25°C,
stored at -25°C for 4 days and then stored at chill temperature (4°C) for a further 4 days. No
difference was found in sensory acceptability between any of the treatments. Drip loss was tower
(P<0.001) in the chilled mashed potato and decreased with decreasing freezing temperature in the
freeze-chilled mashed potato. Freeze-chilling Jed to a finner texture (P<0.001) than chilling alone but
I
\
--.1
the texture softened (P<0.01) with decreasing freezing temperature. Freeze-chilled foods are
potentially more at risk to temperature abuse than chilled products due to the increased amounts of
drip water arising from the freezing/thawing steps. A trial was carried out on the effects of different
storage temperatures on the quality and safety of freeze-chilled mashed potato. No difference in
microbial levels was detected between chil/ and freeze-chil/ at any storage temperature but storage
time and temperature had effects on total viable counts in both chilled andfreeze-chilledproducts.
Keywords. Freeze-chilling, potatoes, green beans, carrots, quality.
The authors are solely respansible for the content of this technical presentation. The technical presentation does not necessarily reflect the
official position of the American Society of Agricultural Engineers (ASAE), and its printing and distribution does not constitute an
endorsement of views whfch may be expressed. Technical presentations are not subject to the fonnal peer review process by ASAE
editorial committees; therefore, they are not to be presented as refereed publications. Citation of this work should state that it is from an
ASAE meeting paper. EXAMPLE: Author's Last Name, Initials. 2002. Title of Presentation. ASAE Meeting Paper No. 02xxxx. St. Joseph,
Mich.: ASAE. For information about securing pennission to reprint or reproduce a technical presentation, please contact ASAE at
hq@asae.org or 616-429-0300 (2950 Niles Road. St. Joseph, Ml 49085-9659 USA).
Introduction
The ready-meals market has grown significantly in Europe over the past decade with the chilled
sector experiencing the most dynamic growth (Mintel, 1997). The strong demand for products
that are fresh, healthy, safe to eat and of good quality have particularly contributed to the growth
within this sector (Mahon et al. 2000). Chilled ready-meals are perceived to be of better quality
than frozen meals (Stringer, 1990). One of the main problems with chilled ready-meals,
however, is their relatively short shelf-life and frozen ready-meals are bought more often due to
their longer shelf-life (Mahon et al. 2000). Along with the advantage of extended shelf-life,
frozen ready-meals also offer better manufacturing and distribution flexibility, food safety and
extended storage time (Kobs, 1997).
Freeze-chilling is a dual process, which involves freezing and frozen storage followed by
thawing and chilled retail display. It has an advantage over chilling as it allows bulk preparation
of frozen products followed by controlled batch release of thawed product into the chill chain. It
has a logistic advantage of enabling 'chilled' products to reach foreign markets more easily.
Freeze-chilling can also reduce the level of product recalls as it enables routine microbiological
tests to be completed before the product is released from the factory (Redmond and Gormley,
2001 ). Freeze-chilling has particular application to complex foods such as ready-meals or
ready-meal components. However, all components must be freeze-thaw stable, including
sauces and gravies. This may require the incorporation of functional ingredients, such as
hydrocolloids.
Tests at The National Food Centre indicated that steamed salmon, steamed broccoli and
reconstituted mashed potato are suitable products for freeze-chilling {O'Leary et al. 2000 ). The
objective of the current study was to examine the effect of freeze-chilling on the quality of
potatoes, carrots and green beans. The effect of different freezing rates and temperature abuse
on the quality offreeze-chilled mashed potato was also examined.
2
Materials and methods
Sample preparation
For the potato trial, approximately 1500g of potatoes (Rooster cultivar) were peeled, washed
and diced (-2-3cm cubes). The potatoes were then boiled on a bench top electric hob oven
(Model 9934, Russell Hobbs) until soft (- 40 mins). Once cooked, the potatoes were mashed
and transferred to plastic containers (500g per container) which were then subjected to one of
the freezing/chilling treatments outlined below. For the carrots and green beans, approximately
350g of product was steamed in a domestic steamer (Tefal Steam Cuisine, Tefal U.K. Ltd.,
London, U.K.) for 20 minutes. Once cooked, the samples were then transferred to airtight
containers and subjected to one of the freezing/chilling treatments outlined below. Reconstituted
potato mash (Chivers Ireland Ltd., Dublin, Ireland) was used for the freezing rate trial. Once
cooled to room temperature, samples of potato (130 g) were placed in plastic pots and
subjected to different freezing rates outlined below.
Freezing treatments
For the potato trial, the potato was subjected to one of the following treatments:
Treatment 1 Freeze-chi//: Product was blast frozen at -30"C for 2.5hrs, then stored at -25°C for
4 days, thawed overnight at 4°C and kept in chmed storage at 4°C for 4 days.
Treatment 2 Freeze: Product was blast frozen at -30"C for 2.5hrs and stored at -25"C for 4
days, then thawed overnight at 4"C.
Treatment 3 Chill: Product was placed in chilled storage at 4
·c for 4 days
Treatment 4 Fresh: Product was cooked and tested on day of analysis
For the carrots and green beans, the products were subjected to the same treatments as the
potato but the time in frozen and chilled storage was increased from 4 to 7 days.
f'or the freezing rate trial, the freezing stage of the freeze-chill process was carried out using a
liquid nitrogen cryogenic environmental chamber (CM-2000, Carburos Metalicos, Madrid,
Spain). The pots of mashed potato were frozen at -30, -60 or -90°C to an internal temperature of
-25°C, stored at -25°C for 4 days in a chest freezer and then thawed and stored at chill
3
temperature (4°C) for a further 4 days. A control consisted of mashed potato samples that had
been chilled for 4 days at 4°C (i.e. no freezing step).
Texture measurement
For the potatoes a cylindrical probe (d 12.5 mm) attached to a Kramer shear press (Alto
Precision Metals Engineering Inc., Maryland, USA) was lowered (entry speed 4.5 mm/s; exit
speed 5.5 mm/s; penetration depth 30 mm) into a pot containing 130 g (± 1 g) of potato sample
and the maximum penetration force (N) was recorded. For the carrots and green beans, texture
was measured using a T 2000 Texture System (Food Technology Corporation, Maryland, USA)
fitted with a standard Kramer shear cell (entry speed -4.3 mmfs) using 100g of product.
Measurements were made in duplicate on a single sample per treatment after chilled storage.
Centrifugal drip loss
Drip loss from the products was assessed after chilled storage by measuring the water loss after
centrifugation according to the method of Anese and Gormley (1996). Approximately 3 g of
product was accurately weighed into a paper filter thimble and placed in a centrifuge tube
containing a layer of glass beads 20 mm deep. Samples were centrifuged at 223 x g for 10 min
at 10°C using a MSE Mistral 30001 (MSE Ltd., Leicester, UK). After centrifugation the samples
were removed and reweighed. Percentage drip loss was expressed as follows:
Drip loss (%) = (wi -wt} x 100
wi
where wi is the initial weight, and wt is the final weight of the sample. Measurements were made
in duplicate on a single sample per treatment.
Taste panel acceptability
Taste panel tests were carried out on the sample range after chilled storage. For each replicate,
fifteen panellists, experienced in sensory analysis, were presented with four heated samples
(approximately 20 g) per sitting, i.e. one sample from each of the four freezingfchilling
treatments. The panellists were asked to score the samples on a 5 cm line scale (with no
divisions) with end-points of 'unacceptable' (0) and 'very acceptable' {5). The point marked on
the line by ~ach
panellist was measured and the mean score for each treatment was calculated.
4
Vitamin C
Vitamin C content was measured tor the potato samples after chilled storage using the 2, 6
dichloroindophenol titrimetric method (FWTG, 1997). Measurements were made in duplicate on
a single sample per treatment.
Temperature abuse
Pots of mashed potato were either freeze-chilled or chilled as described above and then stored
at 4, 7 or 10°C for 8 days. TVC (total viable count) analysis was carried out on days 1, 4 and 8.
Results and discussion
Texture and centrifugal drip
The texture of mashed potato is of critical importance to its acceptability, a soft mealy texture
being preferred to one that is sticky, cohesive or gluey (Faulks and Griffiths, 1983). Shear force
is a measure of firmness with a high value indicating a firm product. In the potato study, a
significant difference in penetration farce was found between treatments (P<0.001 ). Freezechilling and freezing led to a significant decrease in shear force (firmness) compared to chilling
or preparing fresh. The texture of plant tissues is often damaged during freezing due to the
physical effects of ice and also to chemical effects arising from concentration of solutes in the
unfrozen phase (Fennema, 1993). A significant difference was also found in drip loss between
treatments (P<0.001 ). Freeze-chilling and freezing led to significantly higher drip losses than
._,
''1,
chilled or fresh potato. Again this was due to cell damage due to ice crystal formation during
freezing (Reid, 1990). Similar results for texture and drip loss were also found for carrots.
However, freeze-chilling and freezing had no effect on the texture of green beans. This was
unexpected as previous studies on broccoli and potatoes have found that freeze-chilling leads
to a softer, less firm product than chilling or preparing fresh (O'Leary et al. 2000; Redmond et al.
2001 ). The standard deviation in the texture results was high and this may explain why no
difference was found between treatments.
Sensory analysis
In general, sensory analysis showed that freeze-chilled products were similar in acceptability to
their chilled and frozen counterparts. No significant difference was found in taste panel
acceptability for potatoes (mean value
= 2.6) or carrots
(mean value
=-2.8) between freeze5
chilling and the other treatments. O'Leary et al. (2000) found similar results for reconstituted
mashed potato and broccoli. For green beans, the freeze-chilled product was more acceptable
than the fresh product (P<0.05) (2.5 and 1.9 respectively) and similar to the chilled and frozen
products (2.5 and 2.6 respectively).
For the freezing rate experiment, increasing the freezing rate had no significant effect on
product acceptability (mean value= 2.18). Some authors have found that a faster freezing rate
produces a high quality product (Novak and Ramachandra, 1966; Hill and-<31ew, 1973; Childers
and Kayfus, 1982), whilst others have found that product quality is not influenced by freezing
rate {Cunningham and Lohmeyer, 1972; Streeter and Spencer, 1973).
Vitamin C
A significant difference in the vitamin C content of mashed potato was found between
treatments (P<0.001 ). As expected the fresh potatoes had a higher vitamin C content (2.9
mg/1 OOg) than all the other treatments. Chilled and freeze-chilled potatoes had the lowest
vitamin C content (1.0 and 0.9 mg/1 OOg respectively). This is consistent with other reports
(Augustin et al. 1982; Bognar et af. 1990) which state that vitamin C loss is greater at chill
temperatures. Several authors have found that vitamin C loss in vegetables during frozen
storage is relatively small (Bender, 1993; Favell, 1998; lisiewska and Kmiecik, 1996), whereas
losses during chilling can be as high as 40% after 3 days in chilled storage (Williams et al.
1995). Increasing the freezing rate had no effect on the vitamin C content of reconstituted potato
mash.
Freezing rates
( \
Figure 1 shows the core potato temperature profiles in the pots for the three different freezing
regimes. As expected, the lowest freezing temperature (-90 "C) led to the fastest reduction in
temperature (P<0.001 ). Faster freezing rates can result in a better quality product due to the
formation of small intracellular ice crystals as opposed to large ones formed during slow
freezing (Fennema, 1989; Karel et al. 1975; Scholey, 1970).
6
25
20
15
10
0
"-
-"
5
I!
0
E
-5
I!!
8.
{!
-10
-15
'
-20
.1
-25
0
4
s
12
16
m
~~
a
~
~
M
~
m
$
oo
~
~
n
ro
Time(min)
I-<>- -30"G ......- -60'G -+- -90'G I
Figure 1 Average core temperatures for reconstituted mashed potato during freezing at -30°C, -
60°C, and -90°C
One of the major textural problems with reconstituted mash is stickiness/firmness. This may be
due to an excessive amount of extracellular 'free starch' produced both by diffusion of starch
through the cell walls during cooking and by rupture of the cooked cell walls during mashing and
mixing (Faulks and Griffiths, 1983). Ice crystal formation during freezing leads to further
destruction of cell walls and therefore more 'free starch'. This may explain why the frozen
reconstituted mashed potato was firmer than the chilled reconstituted mashed potato. Lowering
the freezing temperature resulted in a softer product, however the effect was non-linear. Drip
loss was lower for the chilled reconstituted mashed potato (0.65%) than for the freeze-chilled
samples (17%) (P<0.001 ). Drip loss decreased linearly (P<0.001) with freezing temperature
(20.7% at -30°C, 18.1% at -60°C, 12.1% at -90°C). This was to be expected as faster freezing
rates mean smaller ice crystals, less damage to the cell structure, and therefore less drip (llR,
1986).
7
Temperature abuse
The limiting factor for the shelf-life of freeze-chilled foods is usually the chill phase as chilled
foods are particularly susceptible to microbial problems. Failure to maintain proper refrigeration
is probably the single most cited hazard associated with chilled foods (Brackett, 1992). There is
also a possibility that freeze-chilled foods could be more susceptible to microbial growth due to
the presence of nutrients in the drip, and also because freezing may open up the cell structure.
No difference in microbial levels was detected between chilled and freeze-chilled mashed potato
at any storage temperature. Storage time (up to 8 days) had little effect on microbial count at
4 °C (log 1 at day 1; log 2.3 at day 8) but led to increased growth at 7°C (log 1.1 at day 1; log 4.2
at day 8) and 1o•c (log 1.1 at day 1; log 6.9 at day 8). As expected, increasing storage
temperature (4°C to 10°C) led to a significant increase in microbial growth by day 4 of storage
for both chilled and freeze-chilled mash (Fig 2). These results suggest that freeze-chilled
products can be treated as chilled products during distribution and retail display.
a~
7
1114°C
Cl 6
fil7°C
-u
: :i
5
g>4
::::. 3
0
i:=
2
1
(
i
\
0
Oil! ~
1
Freeze-chill
~1
Qiilf ~
8
Freeze.dill
~8
Figure 2 Effect of storage time and temperature on TVC values of freeze-chilled and chilled
mashed potato
Conclusion
In general, sensory analysis showed that freeze-chilled products were similar in quality to their
chilled or frozen counterparts. There were some differences between the freeze-chilled and
8
chilled products in instrumental texture assessment and centrifugal drip loss due to cell damage
arising from the freezing step. Increasing the freezing rate during freeze-chilling of reconstituted
mashed potato led to a reduction in drip loss and a softer product. However, these differences
did not impact on sensory analysis and, therefore, there is little advantage in using lower
freezing temperatures. No difference in microbial levels was detected between chilled and
freeze-chilled mashed potato at any storage temperature, which suggests that freeze-chilled
products should be treated as chilled products during distribution and retail display. Storage
time and temperature had an effect on total viable counts in both chilled and freeze-chilled
products and careful temperature control should be exercised to ensure the quality and safety of
these products. Overall, results showed that freeze-chilling has potential to improve the flexibility
of production for many ready-meal components.
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10
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11