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The effect of storage temperature on the quality and formation of blooming defects in chocolate confectionery

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The study aimed at assessing changes in the quality of certain types of chocolate products over the storage period with particular focus on the formation and development of fat and sugar bloom in chocolate products. Seven products were selected in collaboration with a chocolate factory to undergo monitoring and analysis and stored at four temperature regimens (6 °C, 12 °C, 20 °C and 30 °C). Five samplings were carried out over the storing period (18 weeks) for evaluation of the dynamics of changes in their quality. Each sampling was accompanied by sensory evaluation; selected physical attributes were also analysed: Changes in colour (ΔE*ab) within the CIE (L*a*b) system and changes in hardness using the TIRAtest 27025. The results showed a significant effect of storing temperature on the intensity of changes in the quality of products. The results of sensory evaluation of selected products showed that the highest quality for the majority of descriptors was achieved by products stored at temperatures of 6 °C and 12 °C. As regards samples stored under the temperature regimen of 20 °C, the products started to show visible differences, caused primarily by the formation of fat bloom while storing at 30 °C proved to be extremely unsuitable for all the tested products. Since storing temperatures of 6, 12 and 20 °C did not considerably affect hardness and colour of each product, no distinct changes occurred under such temperature regimens. From the aspect of analytical measurements of colour and hardness of each product, storing at temperatures of 20 °C can be termed appropriate. In all the analyses, the effect of the temperature regimen of 30 °C was significantly negative due to defects caused by blooms on the chocolate, meaning that such temperatures are not advisable for storing chocolate products, even over a short term.
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... Even after ten weeks from the production date, the product's texture stored at 6 °C can be preserved and retains its original attributes. It should keep chocolate products at 12 °C [38]. Ref. ...
... The addition of oil-based additives to chocolate can significantly inhibit the growth of fat blooms. [25] Fat replacemen t Chocolate products containing 6.0 % w/w cocoa butter stearin and 0.15 % w/w sorbitan monostearate can delay fat blooms by 15-45 days [26] Fat replacemen t Chocolate products containing 7.5 % DAG cocoa butter can prevent oil migration caused by a fat bloom [38] Processing treatment Compared to conventional tempering, the Well-tempered β-VI pre-crystallization stage inhibited fat bloom and migration. [29] Processing treatment Using a portable NIR spectrometer in conjunction with a chemometric device, different temperatures can cause changes in the shape of fat polymorphs, resulting in the appearance of fat blooms [43] Processing treatment ...
... significantly reduce the bloom rate in chocolate Processing treatment It is possible to keep chocolate products from blooming by adding maltitol and tagatose sweeteners [31] Processing treatment White chocolate products with stevia and sucralose sweeteners can prevent lower fat blooms if the stevia sweetener content is equal to or greater than the sucralose sweetener content [32] Processing treatment Re-tempering chocolate products can increase fat bloom resistance [34] Processing treatment Without tempering chocolate products, blooming can occur on the 25th day of storage [44] Processing treatment Insufficient tempering time and space for phase separation (particles and fat) resulted in the formation of blooms in chocolate [35] Chocolate storage conditions When chocolate is stored at 20-32 °C, it can bloom [36] Chocolate storage conditions Blooming was observed on the first day of storage at 35 °C. However, after seven days, the sensory quality of chocolate had deteriorated [37] Chocolate storage conditions 12 °C is the optimal temperature for storing chocolate products during their storage period [38] ...
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One of the indications of chocolate product degradation is blooming. It is distinguished by the loss of surface shine, which is replaced by a white coating. These effects are caused by insufficient processing, inappropriate chocolate content, and incompatible storage conditions. It can alter these characteristics to enhance chocolate's resistance to blooming and its texture, flavor, and appearance. Several factors must be considered when creating blooming-resistant chocolate, such as chocolate particle size, fat content, processing techniques, and storage conditions. This concise review will discuss fat blooming in chocolate, from its formation to its contributing factors and methods for resolving it.
... As chocolate is a continuous lipid phase, the structural changes in its fat matter may alter volatile release, thus changing the flavor profile of the chocolate [11,14,17,47,48,56,57,66]. As a consequence, chocolates and the related ingredients under study were chemically checked during the 18 months of storage for peroxide and acidity values, polyphenols, and vitamin E [67]. ...
... In the milk chocolate (M sample), brightness and snap increased over time (Figure 2), whereas the intensity of brightness remained constant in D, where the snap became less intense from t0 to t4 (Figure 2a). This was in accordance with Machálková et al. [66], who found a slight deterioration of some mechanical descriptors in the chocolate samples stored at 20 • C. The firmness did not change significantly in D and M samples (Figure 2a,b), while the melting dropped in G and M chocolate (Figure 2c,b). In this regard, Thamke et al. [68] concluded that chocolate with a lower cocoa content was characterized by the greatest melting and creaminess, while the product with the highest cocoa content was characterized as dry dough. ...
... Although D chocolate showed an important loss of polyphenols ( Figure 1B), it maintained the highest content at the end of storage (t4) when the astringency was perceived to be at a medium level, contrary to M and G chocolate (Figure 2b,c). Studies [11][12][13]66,67] have already observed the depletion of polyphenols in cocoa-based products during storage, correlating this loss with their oxidation in the corresponding quinones, which might lead to increases in bitterness, as outlined in D chocolate (Figure 2a). In the same sample, starting from t2, some panelists marked descriptors related to oxidation as "pungent", "closed", "cork", and "dried fig". ...
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Background: While there has been an increasing interest in the health properties of chocolate, limited research has looked into the changes of antioxidants occurring in the time span from production to the best before date, which was a period of 18 months in this study. Methods: Humidity, ash, pH, acidity, fiber, carotenoids, retinols, tocopherols, sugars, proteins, theobromine, caffeine, polyphenols, fats, the peroxide value, organic acids, and volatile compounds, along with the sensory profile, were monitored at 18-week intervals for 18 months under conditions simulating a factory warehouse or a point of sale. Results: At the end of the storage period, more polyphenols were lost (64% and 87%) than vitamin E (5% and 14%) in cocoa mass and cocoa powder, respectively. Conversely, a greater loss in vitamin E (34% and 86%) than in polyphenols (19% and 47%) was shown in the hazelnut paste and gianduja chocolate, respectively. The sensory profiling of cocoa mass, cocoa powder, and hazelnut paste revealed increases in grittiness and astringency, as well as decreases in melting, bitterness, and toasted aroma. Moreover, in the hazelnut paste and gianduja chocolate, oiliness increased with a toasted and caramel aroma. Furthermore, dark chocolate was more gritty, acidic, and bitter. Milk chocolate lost its nutty aroma but maintained its sweetness and creaminess. Conclusions: These results should contribute an important reference for companies and consumers, in order to preserve the antioxidants and understand how antioxidants and sensory properties change from the date of production until the best before date.
... Penetration test was used to determine hardness of the chocolate disks and adhesiveness, defined as the work required to pull the sample away from a surface [30][31][32]. Hardness of chocolate is a good parameter that points out proper control of temperature and stability of the fat crystal network formed during tempering process [33,34]. Treated samples (VeC and SuSDC) showed hardness values lower to the control samples (MiC and DaC), respectively (Table 5). ...
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The main physicochemical characteristics of novel artisanal chocolates (both dark and milky) intended for vegan consumers or for those requiring assumption of fewer simple sugars, were analysed. Replacement of milk (with coconut copra, almonds, and soy protein isolates), and sucrose (with coconut sugars, stevia and erythritol, respectively) in dark chocolate, were accounted for by means of texture analysis, rheology, water activity, fatty acid composition, differential scanning calorimetry (DSC) and fast field cycling (FFC) nuclear magnetic resonance (NMR) relaxometry. The vegan sample (i.e., the milk-less one) showed lower values of hardness and adhesiveness as well as a larger peak in the melting behavior at the calorimetric evaluation (DSC). Moreover, the absence of milk resulted in the halving of the yield stress and a decrease in both the apparent and Casson’s viscosity. In the sample of chocolate with less sucrose, the peak temperatures measured at the DSC indicate crystallization of cocoa butter in its best form (Vβ2), unlike in dark chocolate, due to the different sugar composition. Similarly, the Casson yield stress (τ0), increased significantly (almost 70%), with the substitution of sugar. Finally, the results of NMR FFC relaxometry made it possible to identify aggregates of different sizes, laying the basis for its use as a rapid, non-destructive method for chocolate analysis.
... Hardness of chocolate is a good parameter that points out proper control of temperature and stability of the fat crystal network formed during tempering process [24,25]. All treatments (VeC and SuSC) showed hardness values lower compared to the control samples (MiC and DaC) ( Table 4). ...
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The confectionery industry is increasingly adopting new solutions and possible formulations to expand the ranges of chocolate products that support food styles linked to either cultural or health choices. The chemical-physical characteristics of chocolates (dark and milk) produced with traditional formulations or intended for vegan or demanding less simple sugars consumers (with a 10% reduction in calorific value), were analysed. The effects of the substitution of milk with coconut copra, almond and isolated soy proteins, and the replacement of sucrose with coconut sugars, stevia and erythritol, have been accounted for by analysing texture, rheology and water activity, differential scanning calorimetry (DSC) and fast field cycling (FFC) nuclear magnetic resonance (NMR) relaxometry. The plant-based sample showed lower values for hardness and adhesiveness in the texture analysis, and a larger peak in the melting behaviour at the DSC. Moreover, the substitution of milk powder caused more than a halving of the yield stress and a similar decrease in apparent and Casson viscosity. The crystallisation of cocoa butter in the substituted-sugar sample involved the β V form, the most desirable crystal form in high-quality chocolate. Results by FFC NMR relaxometry allowed identification of differently sized aggregates whose chemical nature is discussed. FFC NMR relaxometry data confirm those by rheological and DSC investigations.
... Sugar bloom on the one hand is often provoked by humid storage or rapid temperature changes and leads to the loss of surface gloss. Fat bloom on the other side is also known to cause quality related issues visible as a fine whitish layer [82]. Growth of microorganisms is, however, of minor importance in this product group. ...
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... al. [40], structural changes induced by temperature, or the process of moisture removal, can cause a decrease in the monolayer moisture content. This is as a result of reduction in the number of active polar sites due to chemical and physical changes [41]. Moreover, Labuza et. ...
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