Comparison of air freezing,liquid immersion freezing and pressure shift freezing on freezing time and quality of snakehead (Channa Argus) fillets

The objective of this study was to investigate the freezing time and quality differences in Snakehead fillets frozen by pressure shift freezing (PSF), conventional air freezing (AF) and liquid immersion freezing (LIF) at −20 °C, −40 °C and − 60 °C, respectively. The results showed that liquid immersion freezing at −60 °C maintained the quality best, with a freezing time of 3.62 min and the cross sectional area of 209.11 um². Air freezing at −20 °C had the longest freezing time (184.58 min) and the largest cross sectional area (4470.79 um²), and lowest hardness and springiness of the fillets. Pressure shift freezing did not demonstrate the well established advantages of maintaining better product quality found in similar technique with some other foods. The samples of pressure shift freezing also had higher thawing loss and free water ratio after thawing. Therefore, the liquid immersion freezing at lower temperatures was demonstrated to better maintain the quality of frozen products and held significant potential for commercial application.Industrial relevanceFreezing is a widely used method for extending the shelf life of aquatic products, but some freezing methods, especially the slower ones, often lead to the decrease in the quality and commercial value of frozen products during storage. This paper explored the comparison of industrially used freezing techniques (air freezing and liquid immersion freezing) with the novel pressure shift freezing technique. Liquid immersion freezing at −60 °C was found to be the preferred freezing method for Snakehead fillets, which maintained better frozen product quality, with a simple freezing process and low cost.     

The effect of glaze uptake on storage quality of frozen shrimp

Ice-glazing is applied to protect the frozen shrimp from undesirable quality changes during frozen storage. Effects of initial frozen shrimp temperature on glaze uptake; glazing time on glaze uptake; and different glaze percentage on physical and chemical changes of frozen shrimp during storage were investigated. Shrimps were frozen in a spiral freezing machine (?35 °C/15 min); transferred to the air blast freezer until the core temperature reached ?18 °C, ?25 °C and ?30 °C; submitted to glazing process; and stored at ?18 °C for 180 days. The glazing percentage, pH and N-TVB levels were monitored every 45 days. This study has demonstrated the effectiveness of the glazing process as a protecting agent for frozen shrimp. A reasonable range of water uptake could be between 15% and 20% to guarantee the final quality. Therefore, it is important to prevent temperature fluctuations during transportation and storage to maintain the quality of the frozen shrimps.     

Impacts of Low and Ultra-Low Temperature Freezing on Retrogradation Properties of Rice Amylopectin During Storage

Amylopectin retrogradation is a serious problem in starch-based ready meals. In the current research, rice amylopectin was frozen by low temperature (−20, −30, and −60°C) and ultra-low temperature (−100°C), and then stored at 4°C for 21 days or at −18°C for up to 5 months to evaluate the retrogradation properties. Amylopectin retrogradation enthalpy of rice was determined by a differential scanning calorimetry. The results showed that low temperature and ultra-low temperature freezing can effectively retard amylopectin retrogradation during the freezing process and during frozen storage (−18°C) for at least 5 months. However, rice amylopectin still retrograded after the freezing process during chill storage at 4°C. The methods of low and ultra-low temperature freezing combined with frozen storage might be potentially very useful for food industry to produce high quality starch-based ready to eat meals.     

Effect of different treatments on the stability of lysozyme,lactoferrin and β‐lactoglobulin in donkey's milk

The aim of this study was to investigate the effects of freezing and heat treatments at different temperatures on the stability of the main whey proteins of donkey milk in comparison with those obtained from colostrum and raw milk. Samples subjected to heat treatment at 85 °C showed greater loss of stability, with levels decreasing by 60% and 87% for lysozyme and β‐lactoglobulin, respectively. Lactoferrin completely disappeared at heat treatments higher than 65 °C. Colostrum contained the highest lactoferrin and β‐lactoglobulin concentrations, however, lysozyme was found to be present at similar concentrations in colostrum, raw, frozen and heat‐treated milk at temperatures lower than 85 °C.     

Influence of pressurised cryogenic nitrogen technology on Arthrospira platensis (spirulina) preservation during storage

In this study, preservation of spirulina using the new pressurised cryogenic nitrogen technology (PCN) was compared to classical methods used in laboratories and industry. Spirulina morphology was better preserved by PCN compared to unpressurised cryogeny and classical freezing at −20 °C that led to cells fragmentation. A 25% loss of Phycocyanin-C content against 60% were measured after 98 days storage for 6-Bar PCN process and frozen samples, respectively. The Total AntiOxidant Power (PAOT Liquid Technology^®) was used for determination of total antioxidant and oxidant power of spirulina extracts. PAOT value of PCN samples was 50% higher than the frozen sample. From ABTS measurements on PCN spirulina fractions sonicated or not, it was suggested that pressurisation at 6 bars allowed a better preservation of free antioxidants (outside the cells) due to replacement of oxygen by nitrogen in the frozen beads. After dehydration, phycocyanin-C content variation during storage at 20 °C and 33% RH showed higher loss for freeze-dried spirulina treated at 0 compared to 6 Bars.     

Low-temperature transitions in cod and tuna determined by differential scanning calorimetry

Differential scanning calorimetry measurements have revealed different thermal transitions in cod and tuna samples. Transition temperatures detected at −11°C, −15°C and −21°C were highly dependent on the annealing temperature. In tuna muscle an additional transition was observed at −72°C. This transition appeared differently than the thermal events observed at higher temperatures, as it spanned a broad temperature interval of 25°C. The transition was comparable to low-temperature glass transitions reported in protein-rich systems. No transition at this low temperature was detected in cod samples. The transitions observed at higher temperatures (−11°C to −21°C) may possibly stem from a glassy matrix containing muscle proteins. However, the presence of a glass transition at −11°C was in disagreement with the low storage stability at −18°C during practical time scales. It was proposed that freezing of cod could be associated with more than one glass transition, with a glass transition at a temperature lower than −11°C being too small to be detectable with instrument, yet governing important deterioration processes. In order to optimize frozen storage conditions, the relationship between deterioration processes important for preservation of quality and glass transition temperatures still needs to be established.     

Textural and Microstructural Changes in Frozen Stored Sardine Mince Gels

The freezing of sardine mince gels produced slight alterations in texture, microstructure and degree of chemical aggregation of proteins, irrespective of freezing temperature (– 18°C or – 40°C). The most noticeable changes took place during frozen storage 3 mo, particularly in gels frozen at – 18°C which were strongly affected by storage temperature (– 12°C or – 18°C), unlike those frozen at – 40°C. Better gel integrity was found in those frozen at – 40°C, where cavities were more numerous, but smaller and more evenly distributed than in gels frozen at – 18°C.     

Influence of vegetable shortening and emulsifiers on the unfrozen water content and textural properties of frozen French bread dough

The influence of vegetable shortening (VS) and emulsifiers (calcium stearoyl-2-lactylate (CSL) and polysorbate 80 (PS80)) on frozen French bread dough has been studied. Eight formulations without yeast were used with different quantities of VS, CSL and PS80. Dough was prepared by mixing all ingredients in a dough mixer at two speeds. The fresh dough was divided into 60 g pieces and molded. Fresh dough samples were also collected for water content and textural analyses. The dough pieces were packed, frozen in a freezer at −30°C and stored at −18°C up to 56 days. After 2, 7, 21, 28 and 56 days of frozen storage, samples were removed from the freezer, thawed at ambient temperature and textural analyses were conducted.The enthalpy of freezable water on fresh bread dough was determined by Differential Scanning Calorimetry (DSC) at the heating rate of 3°C/min, temperature range of −40°C to 20°C. The value of unfrozen water was 0.30–0.34 g H₂O/g solids and additives used during the storage up to 56 days significantly affected the textural properties of frozen dough.     

Effects of the freezing process on proteolysis during the ripening of Port Salut Argentino cheeses

The effect of freezing at −30 °C, frozen storage at −22 °C for 30 days and thawing at 5 °C on proteolysis during ripening of Port Salut Argentino cheese was studied. Cheeses were sampled at different ripening times (1, 6, 13, 27 and 56 days) and two sampling zones (central and external). Moisture content, salt concentration and RP-HPLC of the nitrogenous fractions (water-insoluble fraction, water-soluble fraction and free amino acids in the sulfosalicylic acid-soluble fraction) were analysed. The freezing process did not affect moisture and salt contents at the beginning of the ripening period nor moisture and salt redistribution during the ripening period studied. However, the freezing process affected proteolysis during ripening of Port Salut Argentino cheeses that had been frozen prior to ripening. There was increased breakdown of α_s1-casein and α_s1-I-casein, and increased breakdown of peptides of the water-soluble fraction (including α_s1-CN (f1-23)) along with an early development of free amino acids.     

Changes in texture,microstructure and nutritional quality of carrot slices during blanching and freezing

Thermal processing of vegetables has pronounced effects on the cell structure, often lowering the final textural properties of the product. In order to investigate the effect of thermal processing on carrot, slices were subjected to different blanching and freezing treatments before frozen storage. Microwave-, steam- or water-blanched material was frozen and then stored at −24 °C. Steam-blanched carrots were subjected to blast freezing or cryogenic freezing at different temperatures before frozen storage. The influence of these process conditions on the texture (maximum load and slope), microstructure, dry matter, sugars, carotene and drip loss was investigated. Microwave blanching differed from the other blanching methods by resulting in a heterogenic cell structure. The content of dry matter, carotene and sucrose was higher following microwave blanching. Blast freezing resulted in low maximum load which seemed to be caused by major tissue damage. Concerning cryogenic freezing, lowering the temperature from −30 °C to −70 °C resulted in better preservation of the native microstructure together with an increase in maximum load, which was most pronounced after one month of storage. No significant effect was observed when lowering the temperature from −30 °C to −70 °C for any of the other measured parameters. © 1999 Society of Chemical Industry     

Effect of frozen storage on thermal stability of sarcoplasmic protein and myofibrillar protein from common carp (Cyprinus carpio) muscle

Thermal stability of sarcoplasmic protein and myofibrillar protein extracted from fresh and frozen common carp was comparatively studied. Total sulphydryl content (SH) in sarcoplasmic protein solution from 5‐month frozen carp decreased by 19.43% compared with fresh sample. The SDS‐PAGE patterns showed that all the bands of sarcoplasmic protein from frozen‐stored samples were almost invisible at 80 °C. Myofibrillar protein from fresh sample exhibited lower turbidity and surface hydrophobicity and higher Ca²⁺‐ATPase activity and SH content than frozen‐stored sample when heated from 20 to 80 °C. The Ca²⁺‐ATPase activity from fresh (M0), 2 (M2)‐ and 5 (M5)‐month frozen‐stored carp was completely lost at 48, 46 and 46 °C, respectively. When heated to 80 °C, the SH content of myofibrillar solutions in M0, M2 and M5 decreased by 26%, 60% and 70%, respectively. Sarcoplasmic and myofibrillar proteins from frozen carp were more susceptible to aggregate during heating treatment.     

BIOCHEMICAL AND MORPHOLOGICAL CHANGES IN GRASS SHRIMP (PENAEUS MONODON) MUSCLE FOLLOWING FREEZING BY AIR BLAST AND LIQUID NITROGEN METHODS

Grass shrimp (Penaeus monodon) at prerigor stage were frozen at rates ranging from 3.41 to 16.1 cm/h by using an air blast freezer at –35C or a liquid nitrogen freezer at – 80, – 100 and – 120C. Immediately after freezing, the spacing between muscle fiber bundles was larger (21.3 ± 5.7 μm) in shrimp frozen at 3.4 cm/h than in shrimp frozen at 8.6 ～ 16.1 cm/h (6.0 ± 0.6 to 8.8 ± 1.1 μm, respectively). The spacing between fibers increased during frozen storage at – 20C and remained different for slow and fast frozen samples within 4 weeks. The lysosomal fraction from fresh shrimp had more cathepsin D-like activity (187 units/mg protein) than that from shrimp frozen at 10.2 cm/h (179 units/mg protein) and at 3.4 cm/h (86 units/mg protein). During frozen storage at – 20C the cathepsin D-like activity of intact lysosomes decreased and was negligible after 4 weeks. The solubility of muscle protein in 0.6 M KCl was not consistently different in samples frozen by different methods and stored at – 20C for 4 weeks. Liquid nitrogen freezing produced frozen shrimp of higher muscle integrity than air blast. But the differences disappeared after one-month storage at – 20C.     

Evolution of quality parameters of high pressure processing (HPP) pretreated albacore (Thunnus alalunga) during long-term frozen storage

The aim of this work was to study the application of high pressure processing (HPP) before freezing for maintaining as much as possible the fresh characteristics of albacore steaks after long-term storage. HPP treatments were applied at 200 MPa for 0–6 min. Then, samples were immediately frozen (−20 °C) and stored (−20 °C) for up to 12 months. Once thawed (4 °C; 24 h), weight losses, color, texture, lipid oxidation (TBARS) and salt-soluble protein content were analyzed.After 12 months of frozen storage, 200 MPa for 6 min minimized thawing loss inherent to freezing and frozen storage and decreased TBARS (53.9%) with respect to the control. However, it resulted in changes in color (higher L*, b* and ΔE values) and texture (higher adhesiveness and springiness) and decreased the salt-soluble protein content with respect to non-pretreated samples. Nevertheless, after cooking, there were no differences in color and texture between HPP pretreated fish and the controls.     

Effect of freezing/thawing conditions and long‐term frozen storage on the quality of mashed potatoes

The effects of freezing temperature (−80, −40 or −24 °C) and thawing mode (microwave or overnight at 4 °C) on quality parameters of mashed potatoes made from tubers (cv Kennebec) and from potato flakes were examined, as was the effect of long‐term frozen storage on the quality of mashed potatoes. Mashed potatoes were tested for texture profile analysis (TPA) and cone penetration, oscillatory and steady rheometry, colour, dry matter, Brix and sensory analyses. In natural mashed potatoes, TPA hardness and oscillatory parameters showed that processing resulted in a softer product than the fresh control. The parameters were lower in the samples thawed at 4 °C than in those thawed by microwave at all the freezing temperatures used, which may be ascribed to gelatinisation of the starch released from damaged cells. Differences from the freshly prepared product decreased when the samples were frozen at −80 °C and thawed by microwave. No difference was found in sensory acceptability between samples frozen at −80 and −40 °C, which probably reflects the panellists' mixed preferences for air‐thawed versus microwave‐thawed samples. Increasing the time in frozen storage led to a natural mash with a firmer texture, higher L*/b* value and Brix; nonetheless, panellists found the samples at 0, 3 and 12 months of frozen storage equally acceptable. In commercial mash, penetration and oscillatory parameters showed that processing made for a firmer product than the fresh control, probably owing to retrogradation of gelatinised starch. Thawing mode had a significant effect on parameters, which were lower in the samples thawed at 4 °C. The structure and quality of commercial mash was more detrimentally affected by freezing and, therefore, we would not recommend either freezing or frozen storage of this mashed potato in the used conditions. Natural mash made from Kennebec potatoes should be frozen quickly and thawed by microwave in the conditions described to obtain a product more similar to that freshly made. If the samples are frozen by air blasting at −40 °C, the product can withstand frozen storage for one year. Copyright © 2005 Society of Chemical Industry     

Conventional freezing plus high pressure–low temperature treatment: Physical properties,microbial quality and storage stability of beef meat

Meat high-hydrostatic pressure treatment causes severe decolouration, preventing its commercialisation due to consumer rejection. Novel procedures involving product freezing plus low-temperature pressure processing are here investigated. Room temperature (20 °C) pressurisation (650 MPa/10 min) and air blast freezing (−30 °C) are compared to air blast freezing plus high pressure at subzero temperature (−35 °C) in terms of drip loss, expressible moisture, shear force, colour, microbial quality and storage stability of fresh and salt-added beef samples (Longissimus dorsi muscle). The latter treatment induced solid water transitions among ice phases. Fresh beef high pressure treatment (650 MPa/20 °C/10 min) increased significantly expressible moisture while it decreased in pressurised (650 MPa/−35 °C/10 min) frozen beef. Salt addition reduced high pressure-induced water loss. Treatments studied did not change fresh or salt-added samples shear force. Frozen beef pressurised at low temperature showed L, a and b values after thawing close to fresh samples. However, these samples in frozen state, presented chromatic parameters similar to unfrozen beef pressurised at room temperature. Apparently, freezing protects meat against pressure colour deterioration, fresh colour being recovered after thawing. High pressure processing (20 °C or −35 °C) was very effective reducing aerobic total (2-log₁₀ cycles) and lactic acid bacteria counts (2.4-log₁₀ cycles), in fresh and salt-added samples. Frozen + pressurised beef stored at −18 °C during 45 days recovered its original colour after thawing, similarly to just-treated samples while their counts remain below detection limits during storage.     

Texture and structure of pressure-shift-frozen agar gel with high visco-elasticity

To determine the effects of sucrose and high-pressure-freezing, two kinds of agar gel were compared; A gel with high visco-elasticity and B gel, an ordinary dessert gel. Both agar gels with 0, 5, 10 or 20% sucrose were frozen at 0.1–686 MPa and −20 °C. They were frozen during pressurization, and exothermic peaks were detected at 0.1, 100, 600 and 686 MPa and −20 °C (freezing). However, at 200 MPa, they did not freeze but froze with released pressure (pressure-shift-freezing). Thus, the amount of syneresis from gel pressure-shift-frozen at 200 MPa was smaller than that from gel frozen at other pressures. Also, amount of syneresis from A was smaller than B. In addition, compared to control gels, the appearance of 0% sucrose–agar gels frozen at 0.1, 100, 600 and 686 MPa differed greatly due to syneresis and a volumetric shrinkage of the gel. It was apparent that the rupture stress of the gels decreased, strain and size of ice crystals increased and quality declined. Conversely, due to quick freezing, the texture and structure of both A and B pressure-shift-frozen at 200 MPa were better than the other pressure-treated gels and gels frozen in freezers (−20, −30 or −80 °C) at atmospheric pressure. Consequently, pressure-shift-freezing was more effective. However, texture, structure and syneresis of A were somewhat better than that of B. It was found that the addition of sucrose to the gel was effective in improving the quality of frozen agar gels.     

Rheological and microstructural changes in gels made from high and low quality sardine mince with added egg white during frozen storage

 This paper examines the influence of freezing temperature (–40°C or –18°C) and frozen storage temperature (–18°C or –12°C) on gels made from two different sardine minces (M1, high functional quality; M2, low functional quality), with the addition of egg white as a gel enhancing ingredient. To characterize the washed mince, proximate analyses and protein functionality were determined. Freezing at either –40°C or –18°C caused no drastic changes in gel structure. Throughout the course of frozen storage of all samples, a decrease in the water holding capacity (WHC) was detected, along with an increase in the amount of protein soluble in 8 M urea. At 90 days the gels frozen at –40°C exhibited numerous ice micro-crystals; however, they did not affect the external appearance of the gel and had hardly any effect on gel strength, shear strength, hardness, cohesiveness or elasticity. On the other hand, at 90 days the gels frozen at –18°C and stored at either temperature exhibited large, macroscopically visible ice crystals. In these samples, gel strength and shear strength increased while hardness decreased. No definite changes attributable to mince quality were detected during frozen storage. Received: 23 June 1997     

Effect of freezing conditions and storage on ice crystal and drip volume in turbot (Scophthalmus maximus): Evaluation of pressure shift freezing vs. air-blast freezing

Turbot fillets were frozen either by pressure shift freezing (PSF, 140 MPa, −14°C) or by air-blast freezing (ABF), and then stored at −20°C for 75 days. Smaller and more regular intracellular ice crystals were observed in fillets frozen by PSF compared with air-blast frozen ones. Ice crystals area in PSF samples was approximately 10 times smaller than that of ABF samples, on average. The PSF process reduced thawing drip compared with air-blast freezing. Conversely to this classical freezing process, the storage time did not adversely influence the thawing drip of PSF samples. In addition, PSF appeared to reduce cooking drip after 45 days of storage at −20°C. Differential scanning calorimetry analysis showed a significant reduction of the total enthalpy of denaturation for the pressure shift frozen samples compared to fresh and conventional frozen samples. Besides, a new melting transition appeared on the thermogram of PSF samples at approximately +40°C.     

Freezing and Thawing Conditions Affect the Gel Stability of Different Varieties of Rice Flour

The freeze‐thaw stabilities of three different rice flour gels (amylose rice flour with 28% amylose, Jasmine rice flour with 18% amylose and waxy rice flour with 5% amylose) were studied by first freezing at –18 °C for 22 h and subsequent thawing in a water bath at 30 °C, 60 °C and 90 °C, or by boiling in a microwave oven. The freeze‐thaw stability was determined for five cycles. Starch gels thawed at higher temperature exhibited a lower syneresis value (percent of water separation) than those thawed at lower temperature. Amylose rice flour gels gave the highest syneresis values (especially at the first cycle). The Jasmine rice flour gels gave a higher syneresis value than the waxy rice flour gel. Except for freezing by storage at –18 °C and thawing at 30 °C, there was no separation of water at any cycle when waxy rice flour gel was thawed at any temperature, irrespectively of the freezing methods used. Cryogenic Quick Freezing (CQF) followed by storage at –18 °C and then thawing (by boiling or by incubation at any other temperatures) gave lower syneresis values than all comparable samples frozen by storage at –18 °C. The order of syneresis values for the three types of rice flour was waxy rice flour < Jasmine rice flour < amylose rice flour. The syneresis values and the appearance of starch gels, which had gone through the freeze‐ thaw process, suggested that the order of freeze‐thaw stability of gels for the three types of rice flour was waxy > Jasmine > amylose rice flour.     

Effect of sub‐freezing storage (−6, −9 and −12 °C) on quality and shelf life of beef

Based on the results of low field nuclear magnetic resonance (LF‐NMR) in our current study (the frozen state of ?6, ?9 and ?12 °C were nearly the same with extremely low free water content), ?6, ?9 and ?12 °C was designated as sub‐freezing temperatures. The effects of sub‐freezing storage compared with conventional chilling (4 °C), superchilling (?1 °C) and conventional freezing (?18 °C) on the quality and shelf life of beef were analysed. Results showed that the shelf life of beef is extended to 84 and 126 day at ?6 °C and ?9 °C, respectively. However, the TVB‐N values of the samples stored at ?12 °C and ?18 °C remained below 15 mg/100 g even on 168 day. Furthermore, shear force, colour, pH, thiobarbituric acid reactive substances (TBARS) and sensory properties were also measured. Consequently, the sub‐freezing storage has significantly extended the shelf life of beef compared to chilling and superchilling (P < 0.05). Moreover, no significant difference (P > 0.05) was found between the indicators for quality and shelf life of samples stored at ?12 and ?18 °C throughout 168 days.