Capsule-Packed Freezing of Cooked Rice and Glutinous Rice Cakes

Cooked rice and commercial glutinous rice cakes were frozen by a capsule-packed freezing method we developed, then stored. Characteristics of samples frozen by this new method were compared with those of samples frozen in deep freezers (–20°C and –50°C), or chilled in an ordinary (5°C) or Cold Fog refrigerator (0°C). Texturometer measurements, glucoamylase digestion, and X-ray diffraction analysis of specimens thawed to room temperature indicated that the samples prepared by our new method were superior to those frozen in conventional freezers or chilled in refrigerators. Simulation experiments in a program freezer showed that rapid freezing and adequate tempering were characteristic of our capsule-packed method.     

Programmed Freezing Affects Texture, Pectic Composition and Electron Microscopic Structures of Carrots

Raw and blanched carrots (3 min, boiling water) were frozen at ?2°C, ?3°C, ?4°C or ?5°C/min (final ?20°C or ?50°C) then thawed at 20°C or 100°C. Firmness of thawed raw carrots was: ?5°C > ?4°C > ?3°C > ?2°C/min. Effect of freezing rate on blanched carrots was less than that on raw carrots, but firmness of thawed carrots was not affected by final temperature of freezing. When raw carrots were thawed at 20°C, high methoxyl pectin decreased. Pectin decrease in blanched carrots caused by freezing was greater than that in frozen raw carrots. Effects of slow-freezing, programmed-freezing (slow + quick + slow) and quick-freezing showed quick freezing (—5°C/min) best for texture. As freezing rate decreased, drip increased. A wide difference among experimental samples in fine structure was revealed by cryo-scanning electron microscopy.     

液氮冻结对冻藏雷竹笋品质的影响

目的 研究液氮的3种冻结温度和冻结至3种中心温度对冻藏雷竹笋品质的影响。方法 测定不同液氮冻结温度和中心温度的冻藏雷竹笋的汁液流失率、可溶性固形物和粗纤维含量、硬度、色差、挥发性风味物质和感官评分。结果 液氮冻结温度组中,-60℃组冻结雷竹笋的感官评分、硬度显著低于-90、-120℃组（p<0.05）,而汁液流失率、粗纤维含量、a*值显著高于-90、-120℃组（p<0.05）;雷竹笋原有挥发性风味物质的信号强度为：-120℃>-90℃>-60℃,冻藏过程中产生的挥发性风味物质的信号强度为：-120℃<-90℃<-60℃。中心温度组中,-6℃组冻结雷竹笋的感官评分、硬度显著低于-12、-18℃组（p<0.05）,而汁液流失率、粗纤维含量、a*值、b*值显著高于-12、-18℃组（p<0.05）;雷竹笋原有挥发性风味物质的信号强度为：-18℃>-12℃>-6℃,冻藏过程中产生的挥发性风味物质的信号强度为：-18℃<-12℃<-6℃。-12℃和-18℃组冻藏雷竹笋品质差异不显著。结论 降低液氮冻结温度加快了冻结速率,维持了冻藏雷竹笋较好的感官品质;冻结至中心温度-12℃时,雷竹笋内部大部分水分已完成冻结,此时转移至-18℃冰柜中对雷竹笋组织内部影响不显著（p>0.05）。     

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 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     

Synergistic mechanism of steam blanching and freezing conditions on the texture of frozen yellow peaches based on macroscopic and microscopic properties

Freezing and blanching are essential processing steps in the production of frozen yellow peaches, inevitably leading to texture softening of the fruit. In this study, the synergistic mechanism of stem blanching, freezing conditions (−20°C, −40°C, −80°C, and liquid nitrogen [−173°C]), and sample sizes (cubes, slices, and half peaches) on macroscopic properties of texture, cellular structure, and ice crystal size distribution of frozen yellow peaches were measured. Blanching enhanced the heat and mass transfer rates in the subsequent freezing process. For nonblanched samples, cell membrane integrity was lost at any freezing rate, causing a significant reduction in textural quality. Slow freezing further exacerbated the texture softening, while the ultra-rapid freezing caused structural rupture. For blanched samples, the half peaches softened the most. The water holding capacity and fracture stress were not significantly affected by changes in freezing rate, although the ice crystal size distribution was more susceptible to the freezing rate. Peach cubes that had undergone blanching and rapid freezing (−80°C) experienced 4% less drip loss than nonblanched samples. However, blanching softened yellow peaches more than any freezing conditions. The implementation of uniform and shorter duration blanching, along with rapid freezing, has been proven to be more effective in preserving the texture of frozen yellow peaches. Optimization of the blanching process may be more important than increasing the freezing rate to improve the textural quality of frozen yellow peaches.     

Freezing, thawing and cooking effects on quality profile assessment of green beans (cv. Win)

Results are presented of the effect of freezing followed by thawing (air and water immersion, both at environmental temperature) and cooking (traditional boiling in a covered pot) on quality profile (in terms of objective texture, colour, chlorophylls and pheophytins and sensory attributes) and structure of green beans (cv. Win). Freezing was carried out at three different rates by forced convection with liquid nitrogen vapour. Kramer shear cell (KSC) and Warner–Bratzler (WB) tests were used for objective assessment of the texture. The highest parameter values occurred in beans frozen at the highest rate and air-thawed at the slowest rate. Also, minimum alteration of the rheological behaviour of cooked beans was achieved by freezing at the highest rate. The best parameter for assessing the texture of frozen green beans after thawing and cooking was the Warner–Bratzler slope (S _WB). Coefficients of softening estimated for S _WB in the thawed beans showed that the texture of the beans frozen at −24 °C was almost four and almost five times softer than that of the beans frozen at −70 °C, for air and water thawing respectively. Frozen and thawed green beans were darker than fresh control, whereas freezing prior to cooking produced lighter-coloured beans than direct cooking. The freezing rate affected colour parameters differently depending on the process that followed. When beans were thawed, increasing the freezing rate produced lighter-coloured beans, whereas when beans were cooked, increasing the rate produced darker-coloured beans. No difference was found in sensory assessments between cooked samples frozen at −24 °C, −35 °C and −70 °C, which probably reflects the panellists' mixed preferences for quickly and slowly frozen samples. Scanning electron microscopy (SEM) revealed different degrees of mechanical damage to tissue structure, which accounted for the rheological behaviour of the beans.     

Influence of osmotic dehydration and freezing on the volatile profile of kiwi fruit

The effect of osmotic dehydration on the volatile fraction of kiwi fruit was studied, as well as the effect of freezing and frozen storage. Osmotic treatments were carried out in sucrose solutions until the kiwi fruit reached 30°Brix, at atmospheric pressure (OD) and by applying a vacuum pulse (PVOD), by using 45 and 65°Brix sucrose. Volatile compounds of fresh, dehydrated and frozen-stored (at −18 °C for 1 month) samples were obtained by simultaneous distillation-extraction, and analyzed by GC-MS. Osmotic dehydration provoked formation of esters and a decrease in aldehydes and alcohols, depending on the dehydration treatment applied, which is similar to what occurs during kiwi ripening. A severe reduction of all volatile compounds occurred after one month in frozen storage, which smoothes the changes induced by osmotic treatments. Only small differences between dehydrated and non-pretreated frozen/thawed samples could be recognized.     

Effect of temperature, pressure and calcium soaking pre-treatments and pressure shift freezing on the texture and texture evolution of frozen green bell peppers (Capsicum annuum)

The firmness of green bell pepper (Capsicum annuum) was studied under different processing conditions. Thermal texture degradation kinetics of pepper tissue between 75 and 95 °C could be accurately described by a fractional conversion model. The firmness of pre-processed pepper increased when the samples were submitted to several heat, pressure, and combinations of heat/pressure and calcium soaking pre-treatments. Pre-heating at 55 °C during 60 min and mild heat/high-pressure treatments (200 MPa at 25 °C, 15 min) yielded the best results, which were further improved when combined with calcium soaking. These pre-treatments significantly slowed down thermal texture degradation of pepper at 90 °C, a typical temperature used for pepper blanching prior to freezing. The above-mentioned pre-treated samples showed a significant reduction in firmness when frozen by regular freezing at 0.1 MPa. The same samples showed no changes in firmness when frozen by high-pressure shift freezing at 200 MPa. When freezing was carried out by high-pressure shift and after frozen storage (−18 °C) for 2.5 months, pressure pre-treated pepper showed a better retention of texture than thermal pre-treated pepper.     

Texture and Histological Structure of Carrots Frozen at a Programmed Rate and thawed in an Electrostatic Field

To investigate the most suitable rate of freezing and method for thawing, raw and blanched carrots were frozen with LN₂ (freezing rate: –5°or -2°C/min, final temp: -30°C) using a program freezer (PF), or were frozen using conventional freezers (F: -80°C, -30°and -20°C). Then, they were thawed in five different ways: electrostatic thawing (ET, -3°C, 17 hr); -3°C, 17 hr; 5°C, 17 hr; 20°C, 30 min; 100°C, 3 min. Firmness of thawed carrots and amount of undamaged tissues by LM and TEM observations were greatest to least: PF -5°C/min < PF-2°C/ min <-80°C CF<-30°CF<-20°CF, and ET ≧-3°< 5°< 20°< 100°C, respectively. Results suggest the optimum rate of freezing was -5°C/ min. The frozen disks were defrosted comparatively fast even at -3°by ET. Drip, cell damage and softening of disks were prevented by ET.     

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.     

Changes in optical and mechanical properties during osmodehydrofreezing of kiwi fruit

The influence of osmotic dehydration and freezing–thawing on optical (colour and translucency) and mechanical properties of kiwi slices were analysed. Osmotic treatments were carried out in sucrose solutions up till the soluble solids in kiwi fruit reached 30 °Brix, both at atmospheric pressure (OD) and by applying a vacuum pulse (PVOD). Analyses were carried out on fresh and dehydrated samples before and after frozen storage (at −18 °C for 1 and 30 days). Reflexion spectra (400–700 nm) were measured to obtain the Kubelka–Munk coefficients and CIE-L*a*b* colour co-ordinates. Mechanical properties were analysed through the compression test. A transparency gain was observed in PVOD treated samples and in frozen–thawed samples, which implied a reduction in product clarity and chrome. Colour hue did not change notably, due to either osmotic treatments or freezing. Samples treated with 45 °Brix osmotic solution at atmospheric pressure were the best preserved in mechanical properties after freezing–thawing.     

Pressure-shift freezing and its influence on texture,colour, microstructure and rehydration behaviour of potato cubes

Temperature changes during pressure-shift freezing (400 MPa) of potato cubes and its effects on the drip loss (weight and conductivity), texture (shear and compression tests), colour (L, a, b values), drying behaviour, rehydration properties (water uptake, texture after rehydration) and visible cell damage after thawing (micrographs) were investigated and compared with conventional freezing (0.1 MPa, -30 °C), subsequent frozen storage (-18 °C) or pressure treatment (400 MPa) at +15 :C. Pressure-shift freezing resulted in increased crystallization rates compared to conventional freezing at -30 °C. Crystallization and cooling to ?8 =C took 2.5 min during and after pressure release versus 17 min at atmospheric pressure. Drip loss was reduced from 12.0 to 10.8g/100g. Water uptake during 10 min of rehydration (93.9g/100g compared to 77.4g/100g and incomplete rehydration) and texture values were improved. Browning after thawing or after fluidized bed drying was reduced (increased a value, lower L value), suggesting partial enzyme inactivation during pressure treatment. Differences in colour and texture to the untreated controls were smaller after pressure-shift freezing than after conventional freezing. Cooling to ?30 °C after pressure-shift freezing did not significantly affect the results, whereas subsequent frozen storage at ?18 °C resulted in quality deterioration, as observed after frozen storage of conventionally frozen samples. The improved preservation of cell structure was demonstrated using scanning electron microscopy.     

Studies on freezing of partially dehydrated spinach

Spinach (Spinacea oleracea) was dehydrated at 70 °C, partially dehydrated frozen (dried to its critical moisture ratio and frozen at ?20 °C) and frozen at ?20 °C. Results indicated that the time required for spinach dehydration was 7 h. Thus, the moisture ratio was 10.1 and 0.054 for the fresh and dried spinach, respectively. The critical moisture ratio during dehydration process was 2.20 after 2.65 h of drying time. Reducing sugars, free amino nitrogen, ash, iron and magnesium were slightly decreased in the partially dehydrated frozen spinach relative to the fresh samples. Dehydration markedly degraded the total chlorophyll, chlorophyll a, chlorophyll b, carotenoides and ascorbic acid whereas the freezing of partially-dehydrated spinach and freezing process were less effective. On the other hand, freezing of partially dehydrated spinach increased phaeophytin. There were no changes in pH-values of studied preserved samples. Freezing of partially dehydrated spinach improved the reconstitution of product at 100 °C and at room temperature (25 °C) comparing to dehydration. The drip loss of frozen spinach was 16.4% after 105 min of thawing time. Cooked fresh and frozen spinach were better in colour, flavour, texture, appearance and shape and over-all acceptability than that of dehydrated cooked one. Moreover, freezing of partially dehydrated spinach improved the aforementioned properties.     

Optimisation of freezing process with pressure steaming of potato tissues (cv Monalisa)

Response surface methodology (RSM) was used for determining optimum conditions of the freezing process on pectinesterase (PE) activity, rheological parameters and textural properties in potato tissues. In the process of production of frozen potatoes, the second step of the stepwise blanching prior to freezing was considered as a fixed factor and performed at 97 °C for 2 min as well as the freezing rate in the freezing step itself, which was carried out at −2 °C min⁻¹. The effects of variation in levels of temperature (57.93–72.07 °C) and time (15.86–44.14 min) in the first blanching step on the PE activity were studied using a central composite rotatable design. A Box–Behnken factorial design was used to investigate the effects of simultaneous variation of temperature (60–70 °C) and time (20–40 min) in the first blanching step and steaming temperature (112–122 °C) and time (1–3 min) on rheological parameters and textural properties. Blanching temperature was the independent variable that most influenced either enzymatic activity or rheological parameters. Stationary points showing maximum PE activity had critical temperature and time values of 64.22 °C and 29.37 min before freezing and 64.39 °C and 28.02 min after freezing and steaming of the tissues, and these values were very close to those obtained for some creep compliance parameters. Results show a high correlation between increases in PE activity and tissue firmness below optimum experimental freezing conditions, proving the role of the enzyme as one of the main contributors to the firmness which determines the textural quality of frozen potato tissues. © 1999 Society of Chemical Industry     

THERMAL AND DYNAMIC-MECHANICAL PROPERTIES OF FROZEN WHEAT DOUGHS WITH ADDED SUCROSE,NaCl, ASCORBIC ACID,AND THEIR MIXTURES

The effects of sucrose, NaCl, and ascorbic acid on the physical state of wheat dough at sub-zero temperatures were investigated using Differential Scanning Calorimetry (DSC) and Dynamic-Mechanical Analysis (DMA). The DSC thermograms were obtained for annealed samples by scanning from ?80 to 10°C at 5°C/min. Added sucrose and NaCl decreased the onset of ice melting of doughs, and they were found at ?26°C. Added sucrose and NaCl increased the relative amount of unfrozen water in doughs, while added ascorbic acid had not noticeable effects. DMA measurements were made for annealed samples at a heating rate of 1°C/min from ?150 to 10°C. The loss modulus, G″, of DMA showed an α-relaxation (glass transition), two low temperature relaxations (β and γ), and melting of ice in all doughs with added ingredients.     

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.     

Subcellular Membrane Integrity of Atlantic Cod (Gadus morhua) Myotomal Tissue: Effects of Frozen Storage

The influence of frozen storage on the ultrastructural integrity of Atlantic cod muscle tissue membranes was investigated following three methods of freezing and retention for 12 wk at - 12°C and - 35°C. In comparison to controls (0 wk), extensive membrane condensation associated with sarcoplasmic reticulum was apparent in samples stored for 12 wk at - 12°C. The effects were observed to a much lesser extent in samples retained for 12 wk at – 35°C. It was apparent that cryogenic, plate or blast freezing techniques showed no measurable influence on the observed membrane condensation and that such ultrastructural changes resulted as a consequence of relatively high (–12°C) subfreezing temperatures.     

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     

Structure of northern snakehead (Channa argus) meat: Effects of freezing method and frozen storage

This study was conducted to investigate the potential of cryogenic freezing with liquid nitrogen in the shelf-life extension of northern snakehead (Channa argus) and clarify the effects of temperature fluctuations after freezing on the quality attributes and tissue microstructure during frozen storage. The fish fillets were frozen by three methods including freezing using an ultra-low-temperature freezer (?80°C) to the core temperature of ?60°C (T1) or ?18°C (T2), or liquid nitrogen (T3) followed by storage at ?20°C for five months. Cryogenic freezing with liquid nitrogen postponed the decrease in pH and protein extractability. Temperature fluctuations after freezing might promote the accretion of ice crystals and resulted in the loss of tissue integrity and disorganization of myofibrils. The microstructural changes contributed greatly to the increased thawing loss and decreased resilience, as indicated by the enlarged extracellular spacing and the flakiness of myofibrils. Cryogenic freezing with liquid nitrogen showed no superiority in maintaining the microstructure of northern snakehead fillets, which was supposedly attributed to the cracking in tissue during freezing and the accretion of ice crystals during frozen storage.