Fat Bloom in Chocolate and Compound Coatings
Fat Bloom in Chocolate and Compound Coatings
Fat Bloom in Chocolate and Compound Coatings
DOI 10.1002/ejlt.200400938
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1 Introduction
The Olmec civilization (1500 BC) was the first to transform the cocoa bean into a form of chocolate. For a long time, the cocoa bean has been used as a foodstuff as well as currency. It also has had both religious and divine aspects. In the eighteen-century, the Europeans found it had some aphrodisiac properties [1]. Although chocolate is no longer reserved for the elite, from a scientific point of view, chocolate still retains some mysteries. For example, bloom in chocolate, perhaps a less poetic notion but just as much exciting, is still somewhat a mystery. Fat bloom is directly related to the fat in chocolate products, either cocoa butter (CB) or vegetable oils. CB represents not less than 95% of chocolate fat. In the EU, addition of other vegetable fats above this level means the products are named compound coatings. Another type of bloom, sugar bloom, can also occur with humidity problems, but it will not be presented in this review. A bloomed chocolate is characterized by the loss of the initial gloss of surface, giving rise to a more or less white aspect. Furthermore, the bloom can have different appearances, from a uniform dull gray to a marble aspect, as well as from small individual white points to large white spots on the chocolate. It can be due to many factors, including improper processing conditions, composition, and temperature. One of the problems in characterizing
Correspondence: Richard W. Hartel, Department of Food Science, University of Wisconsin, 1605 Linden Drive, Madison, WI 57306, USA. Phone: 11-608-263-1965, Fax: 11-608-2626872; e-mail: [email protected]
bloom problems is its plurality of shape and also of formation conditions. Moreover, differences between products complicate the scientific analysis. Effectively, the kind of fat and emulsifier, the presence and kind of center on which the chocolate is coated are all parameters that can affect the formation and shape of bloom. However, fat bloom has been studied since the beginning of the last century, with an increase in the knowledge of when and where it occurs. Numerous theories have been proposed to explain bloom formation, but so far none has covered all the multiplicity of bloom or taken into account all of the scientific data. Furthermore, underlying questions remain: Do the different aspects correspond to the same bloom mechanism? And, is the bloom mechanism similar for the different chocolate compositions? In this review, we intend to establish a state of knowledge about bloom, to clarify and find some hypothetical links between the multiplicities of bloom, and to propose a diagram to explain the formation mechanism of any bloom. The first two parts describe briefly the properties of the different fats, the chocolate ingredients as well as a brief description of the processes for making chocolates and coatings. These sections are written to provide a common vocabulary and knowledge necessary to understand the rest of the review. After the brief introduction on chocolate ingredients and processing, we present the different types of bloom according to its origin, its physical-chemical properties and the remedies used to avoid the bloom as well as their potential actions. At this point, the different theories of bloom formation will be briefly discussed. Finally, we
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will try to give a global explanation of bloom formation in chocolates and coatings, through a critical analysis of all the data.
Tab. 1. Polymorphic forms as function of the X-ray diffraction characteristics [8]. PolyUnit Cell morphic form Main forms a b X ray diffraction characteristics
Hexagonal One short spacing at 4.15 Orthorhombic Triclinic Two strong short spacing at 3.80 and 4.2 Multiple peaks, and one strong short spacing at 4.6
Eur. J. Lipid Sci. Technol. 106 (2004) 241274 Tab. 2. Triacylglycerol composition of cocoa butter from different geographical sources [10] {. Malaysia Ivory Ghana Ecua- DomiBrazil Coast dor nican Republic [wt-%] PLO PLP OOO POO PLS POP SOO SLS POS PPS SOS PSS SOA SSS
{
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shelf life often more than one year, but this depends on numerous (sometimes unknown) parameters [20]. The most stable form (bVI) cannot be produced directly from the melted chocolate (except by the addition of bVI CB seeds and under very well controlled conditions [21, 22]. Merken and Vaeck [23] and Aronhime et al. [12] debated the true existence of form VI. Based on DSC studies, they argued that the most stable b form corresponded to a phase differing in composition. Recent results of Loisel et al. [20] seemed to confirm the six different polymorphs, by using an apparatus allowing simultaneous DSC and Xray diffraction recording. However, in several studies using real-time X-ray powder diffractometer, a clear distinction between the 2 b forms could not be made [22, 24]. Cocoa butter with high content of SSS exhibited no clear difference between the X-ray patterns of bV and bVI, whereas cocoa butter with high degree of unsaturation (C18:1 and C18:2) showed clear differences between the two b forms. The X-ray pattern depended not only on the origin of CB, but also on the way they were crystallized. [20, 22, 24]. However, cocoa butter did not correspond to homogenous crystalline phase. Loisel et al. demonstrated that two types of crystals were observed simultaneously. The first and main crystal type was composed of monounsaturated TAG; it had similar polymorph than the whole CBs. Whereas the second type, a minority, was constituted of a high content of saturated TAG and a higher concentration of SOS; it showed a different polymorph than CB and a higher melting point. For example in bV CB, the first crystal type had a bV (3L) polymorph and the second had a bV (2L) polymorph. This segregation occurred during the cooling step as well as during storage (but at a slower rate due to the poor mobility of saturated TAG in monounsaturated TAG).
0.4 1.1 0.1 11.0 2.6 12.6 1.8 1.6 46.9 0.7 29.8 0.4 0.9 0.2
0.7 1.7 0.4 1.8 3.7 15.0 2.3 1.7 46.3 0.7 24.0 0.5 0.8 0.4
1.0 1.8 0.8 2.0 3.6 14.5 2.8 2.0 42.8 0.8 26.3 0.6 1.0 0.2
0.5 1.6 0.7 2.7 3.1 14.1 3.3 1.6 45.4 0.8 24.8 0.4 0.8 0.3
0.7 1.8 0.6 3.8 4.2 14.6 4.4 1.8 42.8 0.7 22.8 0.5 1.0 0.4
0.9 1.7 0.7 5.8 3.9 13.9 6.7 2.1 40.2 0.6 21.7 0.5 0.9 0.6
2.2.1.2 Polymorphism
Cocoa butter TAG can crystallize into 6 different polymorphic forms, usually denoted either by Greek letter or Roman numeral (or both) [12, 13]. The melting points of each polymorph of CB are summarized in Tab. 3. In lipids, the most unstable polymorphs (a) form the fastest but then quickly transform to the more stable forms (bV and bVI). In cocoa butter, the forms I, II and III are very unstable and are quickly transformed into more stable forms. Form bV is a relatively stable form found after appropriate cooling of a melted chocolate with
Tab. 3. Melting point of different polymorphic forms of cocoa butter determined by different authors. Vaeck [14] Duck [15] Wille and Lutton [16] Huygherbaert and Hendrickx [17] [7C] 18.0 (g) 23.5 (a) 28.0 (b) 34.5 (b) 17.0 2124 28.0 33.0 34.4 (g) (a) (b) (b) (b) 17.3 (I) 23.3 (II) 25.5 (III) 27.3 (IV) 33.8 (V) 36.3 (VI) 14.916.1 (I) 17.023.2 (II) 22.827.1 (III) 25.127.4 (IV) 31.333.2 (V) 33.836.0 (VI) 13.0 (VI) 20.0 (V) 23.0 (IV) 25.0 (III) 30.0 (II) 33.5 (I) 13.1 (I) 17.1 (II) 22.4 (III) 26.4 (IV) 30.7 (V) 33.8 (VI) Lovegren et al. [18] Davis and Dimick [19]
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 Tab. 5. Total fatty acid composition of palm oil and 3 different non-identified commercial cocoa butter replacers (CBR) [4]. Palm oil CBR-A CBR-B CBR-C
[wt-%] C14 C16 C18 C18:1 C18:2 C18:3 C20 1.2 44.0 4.7 40.0 10.0 1.3 53.5 18.7 25.0 1.5 Trace 0.8 42.0 22.5 31.3 2.8 0.6 0.7 40.2 22.3 35.0 3.2 0.5
Tab. 6. Triacylglycerol composition of cocao butter (CB), cocoa butter equivalent (CBE) and cocoa butter replacer (CBR) [4]. CB CBE Coberine Choclin CBE-A [wt-%] POP{ POS{ SOS{ Others
{
CBR A B C
2.2.3.2 Polymorphism
According to Timms [27], the most comprehensive study on the phase behavior of palm oil has been reported by Persmark. Palm oil is characterized by three polymorphs, but its fractions have a greater complexity. The highest-melting point fraction, consisting mainly of trisaturated TAG, showed the classical a, b, b polymorphism. The middle-melting point fraction (rich in POP) has suba, a and b1 forms, at low temperatures. At 18 7C, the b1 is transformed into a b form that is transformed into the most stable b form when the temperature reaches 30 7C [28, 29]. Hong Yap et al. [30] have described the polymorphic stability of palm oil, palm stearin and hydrogenated palm oil. The hydrogenated oil was very stable in its b form, whereas the palm stearin had a less stable b form (transforming then into the b form). Cottonseed, soybean or rapeseed oils are mainly constituted of C18 fatty acids. After partial hydrogenation, these oils have the same polymorphic behavior as CB [31]. www.ejlst.de
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Tab. 8. Acyl carbon number profile of different fats [38, 39]. Acyl ICCB carbon number FHPKO FPKO Milk fat Milk fat Winter Summer fraction fraction AMF AMF 17S{ 30S{ [%] C26 C28 C30 C32 C34 C36 C38 C40 C42 C44 C46 C48 C50 C52 C54 18.0 46.6 35.4 1.7 2.3 1.9 4.8 7.5 26.9 22.4 12.7 8.0 4.3 2.5 2.2 1.2 1.0 0.8 1.6 2.0 1.8 4.7 7.3 25.8 22.1 13.0 8.4 4.6 2.9 2.4 1.0 1.0 1.3 1.2 1.3 1.8 2.3 6.0 15.8 18.3 11.6 6.8 4.9 4.4 5.5 8.7 7.6 3.7 1.8 2.3 2.0 2.3 4.2 7.4 8.6 7.2 5.9 7.1 9.7 12.4 14.3 10.7 4.2 0.3 0.5 1.1 2.1 5.6 10.8 13.4 10.7 6.6 6.2 6.7 8.7 11.1 10.7 5.6 1.2 1.3 1.8 2.3 6.0 15.8 18.3 11.6 6.8 4.9 4.4 5.5 8.7 7.6 3.7
ICCB, Ivory coast cocoa butter; FHPKO, Fractionated hydrogenated palm kernel oil; FPKO, fractionated palm kernel oil; AMF, anhydrous milk fat.
The hydrogenated fractions of CBS do not need to be tempered, because of the direct crystallization into the stable b crystal. However, they need proper cooling. Rapid cooling to 1012 7C initiates crystallization, and removes the latent heat of fusion.
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 ity. If isosolid lines vary linearly, the fats are totally compatible and miscible, whereas if a depression occurs in the isosolid line, the fats exhibit some incompatibilities. The isosolid diagrams of the most usual fat mixtures observed in the chocolate industry are presented below.
2.2.5.2 Polymorphism
Due to its complex composition, the most stable form of milk fat corresponds to the b polymorph. For the highmelting (HMF) and medium-melting fractions (MMF), the stable polymorph can be b-2 and b-2 (plus some b-3), respectively [49, 50].
Fig. 1. Isosolid phase diagrams of mixtures of cocoa butter (CB) with (A) anhydrous milk fat (AMF) and (B), high melting point fraction (HMF) of milk fat [46].
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Fig. 2. Isosolid phase diagram of mixtures of cocoa butter and coberine [51].
Fig. 3. Isosolid phase diagram of mixtures of cocoa butter and cocoa butter replacer [51].
blend and some eutectic effects were observed. In this case, the two fats exhibit different polymorphism, which usually has a negative effect on the chocolate quality.
also known as chain length structure, corresponds to a repetitive sequence of the acyl chains involved in a unit cell (along the long-chain axis). This difference in crystalline structures is one of the reasons why these two fats are incompatible and it would be better to use degreased cocoa powder to make compound coatings with CBS [52].
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Fig. 4. Isosolid phase diagrams of mixtures of cocoa butter with (A) fractionated palm kernel oil (FPKO), (B) fractionated hydrogenated palm kernel oil and (C) FHPKO with fully hydrogenated palm oil [52].
Fig. 5. Isosolid phase diagrams of mixtures of cocoa butter (CB) with nut oils [53].
2.4 Emulsifiers
Emulsifiers are primarily used to improve the interactions between sugar and fat and thereby reduces the amount of fat needed for a given viscosity. Emulsifiers may also act as bloom inhibitors. They are authorized in chocolate at a level below 1.5% of the total mass; however, a maximal concentration exists for each individual emulsifier (codex alimentarus, standard 147-1985). Soybean lecithin is one of the most common emulsifiers used in chocolates and coatings. However, there are different kinds of emulsifier www.ejlst.de
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Fig. 6. Isosolid phase diagrams of mixtures of low-melting point milk of fat fraction (obtained at 17 7C) with (A) fractionated palm kernel oil (FPKO), (B) fractionated hydrogenated palm kernel oil and (C) FHPKO with fully hydrogenated palm oil [52].
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Fig. 7. Isosolid phase diagrams of high-melting point fraction of milk fat (obtained at 28 7C) with (A) fractionated palm kernel oil (FPKO), (B) fractionated hydrogenated palm kernel oil (FHPKO), and (C) FHPKO with fully hydrogenated palm oil (HPO) [38].
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 that have slightly different effects on chocolates and coatings. The most studied emulsifiers are briefly described [54].
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2.4.1 Lecithin
Commercial lecithin is a complex mixture of compounds, containing primarily phosphatidylcholine (PC), phosphatidylethanolamine (PE), and phosphatidylinositol (PI). Free fatty acids (FFA) also represent a major component (usually more than 30%) in lecithin. It is the most common emulsifier in chocolates and is used for its effects on rheology and fat bloom.
3 Processing
Although chocolate composition varies slightly depending on the chocolate type, average levels of fat, cocoa solids and sugar are around 30, 20 and 50%, respectively [55, 56]. Flavor and emulsifiers are added at a level below 1%. Several processing methods exist for making chocolate, but all have 5 basic steps: Bulk ingredient mixing. Refining. The size of sugar crystals and cocoa solid particles is reduced to obtain the smooth texture of the final product. The chocolate mass is passed through several rollers separated by gaps of decreasing size. Conching. Flavor development, moisture decrease and release of volatiles occur during the conching. The paste is continuously agitated to coat the solid particles by the fat phase [57]. Emulsifiers are added to improve the blend and extra fat is added towards the end of the conching step to obtain the desired viscosity. Tempering. Chocolate must be tempered to control the polymorphism of cocoa butter [13, 5860]. The melted chocolate undergoes a temperature cycle to induce the formation of nuclei in bV form (and also to destroy the other unstable forms). The addition of seed is also used to induce the crystallization step. New tempering method used bVI cocoa butter seed. It facilitated greatly this step that is less sensitive to temperature fluctuation, quicker and gives even better final quality [53]. The seed crystals formed during tempering permit the surrounding liquid TAG to crystallize quickly in the right polymorphic form [61, 62]. Effectively, it is more favorable for TAG to attach to a growing crystal face than to find sufficient energy to create new nuclei [63]. When the seed crystal concentration is sufficiently high (0.5 to 2% of total mass), the chocolate can be used for the production of molded or coated products. Cooling step. The product is cooled before storage to ensure complete solidification of cocoa butter. Proper temperature control during cooling is critical to growth of seed crystals in tempered chocolate. www.ejlst.de
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4 Causes of bloom
Before discussing the mechanisms of bloom, it is essential to describe and understand all the parameters that can induce or enhance bloom formation. Such a classification (according to the bloom origin) is based on wellknown scientific facts and industrial observations. The origins of bloom can be classified according to three main sources: composition, processing and storage conditions. Pictures of bloomed chocolate and compound coatings are presented Fig. 8.
Fig. 8. Pictures of bloomed chocolate due to (A) storage, (B) fat migration, (C) heat hit, (D) over-tempering, (E) non-tempering.
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4.1.1.1 CB with CBS or CBR 4.1.1.1.1 Lauric hard butter (CBS) and cocoa butter
Coatings made with hard lauric butter are very sensitive to the presence of cocoa butter [65, 66]. A eutectic is formed at very low addition levels of CB to CBS. In addition to softening of the mixture, the blend of these two fats promotes bloom formation. A cocoa butter concentration above 4% can result in a bloomed product in a few months and that time drops to less than a week when the concentration is around 10% [6]. If the proportion of CB in CBS is very high, bloom could appear in less than two days [67]. Moreover, in a study comparing FHPKO/CB and FPKO/CB blends, Williams et al. [38] showed that blends with higher SFC had faster bloom formation. The softest compound coatings, so the most affected by the fat incompatibility, were not the most affected by bloom. This effect remains to be explained.
diagram is not automatically associated with the absence of bloom formation as for the case with the milk fat/PKO blend.
4.1.1.2 CBS and CBR with milk fat 4.1.1.2.1 Lauric hard butter (CBS) and milk fat
Milk fat and its fractions enhanced the bloom formation when they were added with lauric hard butter products [46, 39, 68]. In this case, harder milk fat fractions led to quicker bloom appearance in coatings made with CBS [69]. This behavior was opposite of that found in chocolate where harder milk fat fractions are known to prevent bloom. However, the isosolid phase diagrams have the same dilution effect for both CBS and CB (below 30% milk fat, as always found in chocolates and coatings). In a general sense, it appears that the shape of the isosolid phase diagram is not sufficient to predict bloom behavior of a fat mixture. The depression of isosolids lines of CB with addition of milk fat is not associated with bloom, whereas a similar depression of isosolids lines when milk fat is added to CBR leads to bloom formation. Moreover, the absence of a eutectic in the isosolid phase
4.2.1 Tempering
In the case of chocolate made with cocoa butter, tempering has long been recognized as one of the most crucial and essential steps in order to achieve a good and stable final product [80]. Since compound coatings made with CBS crystallize directly in the most stable form (b), they do not need to be tempered prior to cooling. However, some companies choose either to add a nucleating agent (like hardened palm oil) or temper to ensure complete and proper crystallization of lauric-based coatings.
4.2.1.1 Definition
In a review on tempering, Seguine [63] gives a definition of good tempering: At the end of the tempering, the chocolate must have the largest number of the smallest possible crystals, and those crystals must have the right crystalline form (this means polymorph V). In this case, www.ejlst.de
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 Both effects could promote further bloom. Homogenous heat release, which occurs through the inside as well from the outerlayer, is the best way to avoid any tension on the chocolate surface and consequently, reduce subsequent bloom [79].
the chocolate crystallizes quickly with maximal contraction (facilitating the mold release), and the final product has a high gloss, with good resistance to fat bloom and fat migration (in the case of the filled chocolate). The principal effect of tempering is to develop a population of seed crystals that are sufficient to avoid heterogeneous crystallization during cooling [21]. To be effective, tempering must provide a seed concentration between 0.1 to 1.15% of cocoa butter mass [81]. Jewell, however, reported that larger amounts, 2 to 5% of cocoa butter, of seeds were needed for good temper. This difference may be due to differences in seed size, which affects the number of seed crystals. Von Drachenfels et al. [82] specified the importance of crystal size. The smaller and more regular the size of seed crystals, the glossier the chocolate and the greater its bloom resistance. On the other hand, if the crystal size is too large, the crystals tend to re-crystallize during the storage.
4.2.1.3 Over-tempering
The term over-tempered is used when the seed concentration in the melted chocolate mass is too high. The seed concentration may increase due to excessive tempering time. In this case, the extent of crystallization in the mold is not sufficient to produce the desired mass contraction. The molded surface is not bright and the unmolded surface turns a gray dull very quickly [80].
4.3.1.1.1 Low temperature (<18 7C) 4.2.2 Cooling rate 4.2.2.1 Chocolate
For chocolate, the cooling rate is also an important issue in preventing bloom formation. Cooling too fast may induce crystallization of unstable crystal polymorphs as well as formation of hair cracks and pores on the surface. Cebula and Ziegleder [88] reported that storage below 18 7C inhibited storage bloom in chocolate for over one year. The storage of chocolate at low temperature generally minimizes bloom formation; however, even if the storage temperature is low, bloom can occur after more than one year as the chocolate develops a gray dull appearance. In general, the lower the temperature, the lower the bloom risk. www.ejlst.de
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21 7C and high temperatures from 25 to 3238 7C. The residence times at these temperatures varied between 6 and 24 h. They can be equal for the high and low temperature, or they can differ [87, 89102]. The time-temperature parameters are generally determined empirically except for the highest temperature. In general, the high temperatures must be under 32 7C to avoid misinterpretation of results due to melting effects. No published research has attempted to define the effects of each parameter and thus, chocolate bloom tests are still not standardized.
5 Characterization of bloom
Fat bloom can be characterized according to its shape or crystal morphology, composition and polymorphism. In this section, bloom is characterized according to its crystal morphology, composition, polymorphic form of bloom and the porosity of the chocolate.
4.3.2.1 Chocolate
Temperature fluctuations decrease the bloom induction time and increase bloom rate. In chocolate, even small temperature variations increase the rate of bloom formation. Hettich [80] observed a difference in the bloom stability between chocolate stored at 24 7C or at 24 6 1 7C. However, it is difficult to know which is the prevalent factor inducing bloom, the temperature or its fluctuation. Either way, the chocolate develops a more or less intense gray dull appearance. Researchers often use temperature cycling to accelerate the rate of bloom formation. The chocolate is submitted to high and low temperature plateaus over a variable time. The time-temperature parameters vary for different researchers. Low temperatures have varied from 15 to
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enon, but it was also found in the whole chocolate mass. The inside crystals had a more irregular shape with a size from 1 to 5 mm. No published research has focused on the shape of bloom on coatings made with pure CBS. However, this bloom also correspond to pure fat crystal growing on the surface.
Eur. J. Lipid Sci. Technol. 106 (2004) 241274 tion was found to be much lower in bloom than in the normal chocolate. Chaveron et al. [77] studied the bloom of a plain and two filled chocolates. The FA analysis, measured by gas chromatography showed a slight increase in C16:0 and C18:1 concentrations and a decrease of C18:0. Different hazelnut oil contents of the centers did not influence the bloom composition. Adenier et al. [115] confirmed the Chaveron studies, where the composition was very similar between bloom and the initial chocolate. According to Loisel [116], Sato studied the composition of fat bloom on chocolate as a function of the storage temperature. The bloom occurring below 13 7C had a higher POP than POS concentration. The inverse was observed when chocolate was stored above 13 7C (POS was at a higher concentration than POP). Ziegleder et al. [117] found some differences in bloom composition between plain and filled chocolates. They studied seven different plain chocolates and twenty-two other chocolates with different kinds of centers and found that the filled chocolates had a higher OOO concentration in bloom. However, Loisel [116] contested this observation based on lipid mixing rules. According to the phase diagram of SOS and OOO, these two TAG have a very low miscibility at 20 7C, and OOO is liquid under 0 7C [118, 119]. Thus, Loisel concluded that the analyzed blooms from Ziegleder et al. were contaminated by the underlayer of plain chocolate. It is difficult to compare each study, because some are expressed in FA concentration, whereas others analyze for TAG, and the results are often contradictory. Either an increase [114, 116] or a decrease [77, 115] in POP was observed, and in some cases a very slight composition difference between bloom and initial chocolate. However, most studies agree that the center has no influence on the bloom composition. Based on the results available in the published literature, it is difficult to conclude anything about the bloom composition. However, if there is indeed a difference in chemical composition between bloomed and intact chocolate, the differences are very small.
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When 10% of CB was added to the hydrogenated PKO, the bloom also had higher C12:0 (only 3%), but also higher C16:0, C18:0 and C18:1 concentrations, suggesting that the TAG in CB were also incorporated in the bloom crystals [107]. Similarly, in the case of coatings made with hydrogenated coconut oil and CB, Traitler and Dieffenbacher [25] found an increase of SOS (coming from the CB) in bloom, indicating a migration of CB to the surface. In the case of CBR (from soybean or a blend of soybean and cottonseed oils), the fatty acid concentrations of the bloom and the plain chocolate had quite similar values [6].
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 pressure of 180 MPa was used, but not at 80 MPa. The authors explained this by the collapse of structure due to the high pressure used and the low penetration level as the result of the presence of liquid fraction filling the capillaries. So the low level of mercury penetration, as well as the absence of mercury at the center of the chocolate, suggests a poorly connected capillary network. Furthermore, the authors reported that thin dark chocolate layers were totally impervious to gas (at 1 MPa) and no trace of liquid fraction was observed on the surface. Despite these interesting results, many questions remain about the capillary network of chocolate. Recently, Khan et al. [123] highlighted the presence of pores at the surface of milk chocolate by scanning the surface with an atomic force microscope. They estimated the concentration of pores to be thousands/cm2, with pores of 1 to 2.5 mm of depth randomly distributed on the surface.
bloom formation in these coatings, but no evidence for bloom being in the b polymorph was obtained. However, in these studies, the polymorphic form of the bloom crystals themselves was not determined, only that of the mixture of fats. However, Schmelzer and Hartel [69] showed that the addition of 15% of very high melting fraction of milk fat to palm kernel oil permitted the transition from b to b form of the fat, after 3 months of storage. No polymorphic transition was observed below 15%. Liang and Hartel [121] could perhaps reconcile these studies. By differentiating the bloom from the whole piece (bloom carefully removed from surface), they were able to observe the b form in the bloom scrapings while the bulk coating was still in the b form. In the case of coatings made with CBR, Paulicka [122] found a transition from b to b. In this study, the fat was derived from domestic oils by solvent fractionation. The transition associated with bloom was faster when some CB was added. Compound coating bloom has not always been correlated to a polymorphic transition of the fat, as is the case with cocoa butter. However, recent studies clearly document that a polymorphic transformation is associated with onset of bloom in PKO-based compound coatings. Further studies on bloom in compound coatings are needed to verify that the onset of bloom is always accompanied by the appearance of the b polymorph.
5.4 Porosity
In many publications, bloom in chocolate is often described as a process involving the migration by capillary action of a liquid fat to the surface [79]. Loisel et al. [81] considered the chocolate as a porous material and were able to determine, by mercury porosimetry, the porosity volume of well-tempered dark chocolate (bV), under-tempered (bV) and over-tempered (mixture of bV and bVI) chocolates. The bubble air volume due to the process was determined with X-ray radiography to be less than 0.1% of the sample volume. The porosity of normal chocolate was about 1% of the total volume and this increased to 2% for the under-tempered chocolate and 4% for the over-tempered chocolate. These results did not allow determination of the precise pore diameter, but suggested that the chocolate does not have open and interconnected pores with mean diameter larger than 0.4 mm at the surface. Moreover, it seems that the pores are filled by the liquid fraction of CB at room temperature. As a result, it is better to talk about empty cavities rather than pores. The presence of mercury at the sample center is not very clear. Mercury was found at the center when a
Eur. J. Lipid Sci. Technol. 106 (2004) 241274 improved the tempering step, particularly for low-melting point CB. Similar results were obtained with CB removed from its liquid fraction. Another method used to decrease bloom was to add specific TAG to chocolate. SOS and POP or asymmetrical TAG like SSO or PPO were reported to impede the bV to bVI transition, and consequently inhibited bloom [109, 126].
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ited by addition of milk fat and this effect was improved by using the high-melting point TAG of milk fat [127]. At that time, use of milk fat fractions were not economically viable, so research focused on use of hydrogenated fat. Campbell et al. [128] also investigated the effects of hydrogenated milk fat. Dark chocolate made with addition of 2.5% hydrogenated milk fat was four times more bloom resistant than chocolate made with non-hydrogenated milk fat. Furthermore, fully-hydrogenated fat was more effective than partially-hydrogenated fat [93]. However, the amount of fully-hydrogenated fat was lower in order to avoid incompatible fat problems. Hendrickx et al. [129] mentioned, in a study focusing on texture, that substitution of cocoa butter with hydrogenated milk fat delayed or eliminated fat bloom.
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 fat fraction reduced the transition extent but didnt delay it, whereas no effect was found with the low-melting point fraction. These results suggest that the mechanism of bloom inhibition of milk fat in chocolate is related to the inhibition of the polymorphic transition of cocoa butter. However, further research is needed to document this effect.
milk fat fraction was below 41.0 7C. The hardness of chocolate with 2% addition of the same milk fat fractions had similar variations as the SFC behavior. Chocolate was harder when made with the fractions having a melting point above 41.0 7C and was softer with milk fat fraction below 41.0 7C melting point [101]. Timms and Parekh [131] reviewed the different properties of chocolate, particularly SFC, after the addition of different amounts of milk fat products, including whole milk fat, hydrogenated, fractionated or interesterificated milk fat. The effect of milk fat fraction was dependent on temperature of the chocolate. Below 32 7C, SFC decreased when high-melting point milk fat fraction was added and the decrease of SFC was proportional to the amount added. However, the differences in SFC were quite small between the low-melting point milk fat fractions. Above 32 7C, the SFC of chocolate with added high-melting milk fat fraction increased as compared to pure chocolate. Jewell and Bradford found similar results [132]. In summary, the addition of a large amount (.10%) of milk fat decreased the hardness of chocolate, but even with a softened texture, this chocolate was more bloom resistant than normal chocolate [130].
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Tab. 10. Effects of emulsifiers on the improvement of bloom resistance in comparison to chocolate or coating made without emulsifier{. Fat CB 1 lecithin [134] Hydrogenated PKO [135] Fractionated PKO [135] Hydrogenated palm soybean oils [135]
{
DMG
MDG 2
SMS 2
STS = 1 1 11
LMD 2
DATEM PMD 22 2
12 2 =
= = =
bloom development, 1 bloom delay, = similar than the reference; DMG, distilled monoglycerides; MDG, Mono- and di-glycerides; SMS, sorbitan monostearate; STS, sorbitan tristearate; PGE, polyglycerol esters; LMD, lactic esters of mono and diglycerides; DATEM, diacetyl tartic acid esters of monoglycerides; PMD, sodium salt of phosphated mono/diglycerides.
Minor components of fat should be also discussed. In a recent study, Tietz and Hartel [102] reported an antagonistic effect of minor components on bloom as function of their concentration. Use of fat having no minor component or a double concentration increased bloom.
studies have reported an inhibition of the bVbVI transition when emulsifiers were added to fat bulk without sugar [151, 152].
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 efficient when the ester had more than one acid radical per molecule (sorbitan tristerate was more efficient than sorbitan monostearate). Garti et al. [155] also studied the effects of sorbitan ester effects (single or mixed with polysorbate 60) on polymorphism of cocoa butter. They found an increase in the bIV-bV transition rate, but a delay in the bVbVI transition, as was previously found. The same observation was found with the crystallization of palm oil [160, 161]. However, according to Garti et al. [155, 160], the sugar esters must be solid at room temperature (and have a structural compatibility with the fat) to be efficient against the bV bVI transition. Due to the rigid structures (high melting point), the emulsifiers could hinder the motion of TAG that are consequently entrapped in a rigid network. The polymorphic transition would be directly hindered by the rigidity of the sucrose ester. Sucrose esters also delayed nucleation and slowed down the bb polymorphic transition of hydrogenated sunflower oil [162]. Thus, it would act in the same way as the sorbitan ester. In general, FFA or diglyceride are known to inhibit polymorphic transitions, even at low concentration (105). Hernqvist et al. [163, 164] reported the effect of 1,2-DAG on rapeseed oil phase transition and concluded that DAG delayed the b-b transition, more by forming a fat crystal network containing DAG, than by disturbing the crystal lattice. They discussed also the optimal chain length, and concluded that the longest stabilization occurred when the DAG chain length was similar to that of the fatty acids in the TAG. The stabilizing effect decreased with shorter chain length and longer chain length could create some co-crystallization problems. It appears that the most efficient emulsifiers, in terms of bloom inhibition, have three major effects. 1. They improve crystallization by increasing the number of seeds that are formed and reducing the crystal size. 2. They increase the melting point of the fat so the product has a better thermal resistance. 3. They prevent the ultimate polymorphic transition that is always associated with chocolate bloom [165]. These effects are almost similar to the effects of milk fat effects and may be why several authors wondered if the effects of milk fat were due to its minor lipid content, like FFA and partial glycerides, or to the specific TAG composition [86, 102]. www.ejlst.de
Diglycerides (DAG) have also been shown to influence crystallization rate. In a study on the crystallization of palm olein, Siew and Ng [151] found an antagonistic phenomenon of the DAG as function of its configuration. The 1-2 configuration of the DAG delayed nucleation, whereas 1-3 DAG improved crystallization. Growth rate. Smith and Povey [152] reported the effect of free fatty acid (FFA), monoglyceride and 1,2- or 1,3-diglyceride on the growth of trilaurin crystals. FFA and monoglyceride increased slightly the trilaurin crystal growth, but decreased the facet and crystal size, whereas 1,2diglyceride and 1,3-diglyceride (at a higher extent) decreased the crystal growth. The effects were greater when the chain length of glyceride was longer than C12, whereas the used of shorter chain length glycerides did not give as much variation. The inhibiting effect of DAG (without conformation distinction) on CB crystal growth was previously shown by Kattenberg [154]. Melting curve. Addition of minor components can affect fat crystallization, usually decreasing the initial melting point of each polymorph [155]. For example, Wilson [135] found that the most effective anti-bloom emulsifiers acted either by reducing the melting curve of the sample or by increasing the general melting temperature of product, whereas the less effective emulsifier tended to enlarge the melting range of chocolate. Schlichter and Garti [156] found that the sorbitan disturbed the initial natural blend between the low- and high-melting point of cocoa butter TAG. They tended to crystallize separately and their melting peak by DSC were more distinct. Cebula and Smith [157] studied the effect of DAG on crystallization of Coberine (CBE) and found that it enhanced crystallization (occurring sooner) but the following growth rate was reduced. Seed material. Since phospholipids crystallize at higher temperature than TAG, they could act as nuclei or seeds. According to Arruda and Dimick [158], the phospholipid concentration was twelve-fold higher in the seeds (first cocoa butter crystals) than in the bulk, with concentrations of 3.9% to 0.34% in seeds and bulk crystals, respectively. The main phospholipids in the seeds were PE (phosphatidylethanolamine) and PC. Thus, emulsifiers may impact bloom formation by promoting formation of many small fat crystals. Polymorphic effects. In a general review on emulsifiers used in foods, Krog [159] confirmed that the sorbitan esters of palmitic and stearic acids stabilized the intermediate form bV of cocoa butter. This effect was more
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strain it enough to inhibit lipid migration. Some amorphous compounds are known to reduce the mobility of reactants [173, 174].
6.2.1 Tempering
Different chocolates with different ingredients often require different tempering conditions. For example, it is well known that milk chocolate must be cooled to lower temperatures than dark chocolates in tempering to obtain the same extent of crystallization. The key step for chocolate is to form the right concentration of small bV seed crystals by careful control of the temperatures in the tempering unit [63, 175]. Tempering is of course less important for compound coatings, where tempering is often not needed to form the proper extent of crystallization. An alternative method of tempering involves addition of seed crystals to chocolate in order to induce crystallization [80, 176]. Seeding decreases the process time as well as many of the temperature constraints involved in the tempering step. One of the earliest studies on seeding was done by Giddey [21] who used SOS seed in the bVI form and under proper temperature condition to crystallize CB directly into the bVI form. According to van Dongen [167], a chocolate with CB in the bVI form would be impervious to bloom. However, Adenier et al. [86] used CB seeds in the bVI form, but were not able to crystallize either CB or dark chocolate directly into the bVI form. Recently, a new tempering method using bVI CB seeds has been commercialized. This technique allows an easier bV CB crystallization. Even though the chocolate is not in the bVI form, this method increases the bloom stability [53]. The exact effect of seed crystals on the bloom mechanism remains unclear. A systematic method was used to screen the effect of different seeds: bVI CB, b and b SOS, b SSS, b and b BOB (1,3-dibehenoyl-2oleoylglycerol (C22-C18:1-C22). b BOB and b SSS were ineffective due to the TAG packing difference with CB (2L and 3L, respectively). bVI CB and b SOS improved bloom resistance (with 32/20 7C test cycle) when the concentration used was below 2.5%; above this concentration, the seeding promoted bloom. b BOB seeds improved bloom resistance (32/20 7C and 38/20 7C test www.ejlst.de
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cycle) when seed concentration was above 1% [9598, 177]. The high-temperature resistance of chocolate made with BOB seeds was explained by the higher melting point of BOB (51.4 7C). Thus, the BOB seeds did not melt and could act as seeds during the cooling.
6.2.2 Cooling
As already discussed, cooling that is too slow or too quick can induce bloom. For example, rapid cooling produces small cracks and pores on the chocolate surface, enhancing bloom [79]. Rapid cooling may also promote formation of unstable polymorphs in the regions that have cooled too quickly. Proper cooling of both chocolates and compound coatings is needed to protect against early bloom formation.
7 Bloom theories
Since the 50s, several theories or explanations have been proposed to understand and explain bloom formation [91, 99]. Naturally, these theories have changed as new data has been collected. Moreover, bloom theories often do not take into account the whole complexity of the diverse aspects of bloom formation; most describe bloom occurring during storage and cannot explain all the effects of active components. Theories that relate bloom to phase transition, eutectic effect, crystal demixion, and lipid migration are the most common.
Eur. J. Lipid Sci. Technol. 106 (2004) 241274 Such a separation between low- and high-melting point TAG has been observed during the early stages of crystallization. For example, the initial CB crystals formed had higher concentrations of POP, POS and SOS as well as PE and PC [158, 180] under static conditions and higher PSS, SSS and SOS concentration and a lower POS and POP concentration [181183] under dynamic crystallization conditions. The general concentration of glycolipids, phospholipids, saturated FFA and DAG in the initial crystals formed was increased [184]. This heterogeneity of the initial crystals suggests a core seed with a high melting point core composed of trisaturated TAG and minor compounds. Becker [185] showed that two TAG families, POO1SOO1OOO and POS1SOS1POP, formed a stable solid near the CB melting point, but they tended to separate as temperature decreased (below 16 7C), leading to bloom. Unfortunately, this very interesting theory has been contradicted by several authors [78, 91, 104].
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Qualification and quantification of oil migration was highlighted by Adenier et al. [78]. The liquid TAG in the center migrate from into the chocolate at the same time that the chocolate TAG migrate back to the center, but to a lesser extent. Moreover, the migration rate ceases once the equilibrium fat content has been achieved. Oil migration is an attempt to reach an equilibrium state of TAG concentrations between center and coating. Tab. 11 underlines the fatty acid composition of the different parts of a filled chocolate, before and after fat migration. Tab. 11. Relative proportion of fatty acids composition of each moiety of a filled chocolate, before and after migration [115]. Chocolate Initial C16 C18 C18:1 C18:2 25 34.2 36.5 4.2 Filling Initial Chocolate after fat migration 17.6 22.6 52.2 7.6 Filling after migration 9.5 6.4 71.2 12.9 Bloom of filled chocolate 26.2 30.1 40.1 3.6
Recent studies have highlighted very precisely the differences of migration as function of temperature by using magnetic resonance imaging to follow liquid TAG [75, 188, 189]. At 19 7C, liquid fat stayed near the fillingchocolate interface, with concentration increasing with time (migration is limited at this temperature). At 28 7C, the liquid fat moved further and accumulated just below the chocolate-air interface. This last observation suggests that the migration mechanism is not only governed by a TAG concentration difference but also by structural differences in the coatings. Similar results were obtained when the samples were storage up-side down, excluding a mechanism based on gravitational forces. The authors proposed that migration could be due to diffusion as well as capillary attraction. However, for both mechanisms, crystal demixion and oil migration, the main problem is the explanation of the driving force, and how some TAG can crystallize on the surface. Cousens and Wille [75] hypothesized a lower surface free energy at chocolate surface than the oils. The nature of the surface and chocolate porosity may either permit or prevent liquid fat from reaching the surface. For example, it is well known that any scratches on the surface enhance bloom. Adenier et al. [86] found that chocolate covered with aluminum foil was protected against bloom. This suggests that liquid fat reaches the surface by capillarity and then crystallizes to produce bloom. Effectively, liquid oil could not reach the surface www.ejlst.de
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 the polymorphic transition. Sugar and cocoa powder are the only components that remain in the inter-crystal space and appear as white spots on the surface. Similar re-crystallization and rearrangement occurs eventually throughout the bulk of the chocolate.
when a pressure difference does not exist and, in this way, bloom would be inhibited. The only accurate work related to porosity is from Loisel et al. [81]. They found a difference of volume porosity of 1% for normal chocolate and 4% for chocolate in the bVI form. However, the real structure and inter-connectivity of pores are still unknown.
8 Discussion
Numerous theories exist to explain bloom, but so far none seems to cover or explain the entire range of blooms plain chocolate, compound coatings, filled chocolate, during the storage. Before proposing our final statement about bloom, we discuss the different blooms classfied in four categories: 1. Bloom due to under-tempering or melting of tempered chocolate. 2. Bloom due to over-tempering. 3. Bloom due to a problem of incompatible fats, whether due to the initial fat composition or migration of an incompatible fat. 4. Bloom that occurs over time, or storage bloom. The first two types of bloom are specific to chocolate (made with CB), whereas the latter two mechanisms may apply to any kind of chocolate or compound coating. All four bloom mechanisms are due to a stability problem of fat crystals, but at different scales. At this point, storage bloom of chocolate and compound coating may be compared, even though there is some question as to whether the bloom mechanism is similar or not for these different fats.
With over-tempered chocolate, where either too much seed has crystallized or the seed crystals are too large, bloom develops while the chocolate is solidifying. Bloom is maximum at the end of chocolate solidification and does not vary with time (although storage bloom can occur over time as in any chocolate). Bloom appears as a dull gray surface due only to light diffraction from large CB crystals and not to the presence of pure fat crystal on the surface. During cooling, the large and numerous CB crystals formed during tempering deplete the liquid fat in their vicinity, creating a rough surface with cracks and crevices. Incident light is diffracted on this rough surface (due to the crevices and large crystals), giving a dull, whitish-gray appearance [190].
Eur. J. Lipid Sci. Technol. 106 (2004) 241274 likely to re-crystallize into a more stable polymorph, initial at the surface, and appear as visible bloom. Once fat migration and softening occur, the bloom mechanism is similar to that which occurs in storage bloom (next section).
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layer or coated with glaze (e.g., panned chocolate pieces) are quite resistant to bloom, likely because the liquid TAG can not cross to the surface. The rate of migration of liquid TAG may be influenced by numerous factors, including the hardness of the fat (change in liquid fat with temperature), the particulate structure (sugar, cocoa solids, milk solids, etc.), emulsifier interactions and the porosity of the chocolate (cracks and crevices providing access to the surface and capillary forces) [191]. Thus, increased porosity of the chocolate due, for example, to crack and crevice formation from cooling too quickly, results in immediate migration of liquid fat to the surface and rapid onset of bloom.
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Eur. J. Lipid Sci. Technol. 106 (2004) 241274 Once this first step is induced, the formation of a bVI crystal might destabilize the surrounding area and promote additional crystallization of bVI. Moreover, this phase transition corresponds to a mass contraction, which directly affects the cohesion of the mass. The chocolate loses its initial cohesion as empty spaces are created between crystals. It can also lead either to bare sugar surface, or needle-like fat crystals (characteristic of the bVI polymorph). Each of these factors would be sufficient as seeds for further crystallization. The concomitant presence of sites of crystallization and the increase of porosity (from 1 to 4%, permitting the liquid fat content to cross the surface), would permit a quick crystallization of most of the liquid fat content. This re-crystallization of chocolate mass (CB mass and liquid fat content together) would explain the small difference of composition between initial chocolate and bloom composition. Effectively, based on the fatty acid composition variations between initial chocolate and bloom (19.9% C18:1, 211.9% C18 and 14.8% C16), it is difficult to explain that bloom would be only due to: (1) the monounsaturated TAG coming from the liquid content of cocoa butter [115] (If such was the case we should have also an increase of C18 corresponding to the C18:1 increase.). (2) the chocolate mass re-crystallization (composition is not exactly similar between chocolate and bloom). The determination of the TAG composition of the initial site of crystallization (during the first step of bloom formation) would certainly yield interesting information about whether re-crystallization occurs preferentially in the liquid fat content or in the remaining CB crystals. Fig. 9 summarizes the factors that either promote or inhibit bloom development during storage of chocolate. The primary factors discussed previously are contained within this diagram as either bloom activators or bloom inhibitors. The main points related to the mechanism of bloom formation in chocolates are oil migration (with liquid oils dissolving high-melting TAG) due primarily to temperature fluctuations, leading to re-crystallization of fat at the surface in a more stable polymorph and growing in the proper orientation to scatter incident light.
hance the re-crystallization. Moreover, if high-melting point TAG are dissolved, this would decrease the energy needed for the phase transition, since the high-melting TAG increase the barrier energy for each polymorphic transition.
8.4.2 Chocolate
In chocolate, storage bloom covers the surface very uniformly and its composition is not substantially different than the initial composition of the CB (even with filled chocolate). Adenier et al. (1993), for example, showed that bloom had a similar composition as the liquid fraction obtained at 28 7C. A slight increase of C16:0 and C18:1 and slight decrease of C18:0 fatty acids were observed, but the composition of bloom was not significantly different from the CB composition. In this case, the polymorphic transition from bV to bVI is always observed. During the early stages of storage bloom, the chocolate is in the bV polymorph [86]. As bloom is initiated and progresses through the early stages, there is an increase in the amount of the more stable bVI polymorph that can be measured by X-ray diffraction. However, scraping the bloom crystals off the surface for analysis reveals that the bloom crystals are all primarily in the bVI form. As proposed before, this re-crystallization could be due to the crystallization of the most saturated TAG of the liquid fat content that crossed the surface and/or by the polymorphic transition of the CB crystals. It is a first step that initiates bloom by creating site of crystallization. However, in order for visual bloom to be observed, re-crystallization must occur so that spiky crystals emanate from the surface to interfere with light reflection, giving the dull and whitish appearance. Furthermore, if re-crystallization could occur so that the crystals form, for example, in layers, as opposed to spiky crystals emanating from the surface, the chocolate would remain without visual bloom despite the polymorphic transition of the fat. This is most likely what occurred in the study by Bricknell and Hartel (1997), where no visual bloom was observed despite formation of the bVI polymorph. Thus, the polymorphic transition accompanies bloom formation, but by itself is not sufficient to always cause the appearance of visual bloom. Moreover, formation of crystals on the surface of chocolate would have to be easier than in the interior of the chocolate. The energy needed to change the bV-air to bVI-air interface would be lower than that for the bVI/ matter interface. Thus, the first transition would take place on the surface and subsequently move into the bulk of the chocolate.
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bloom in coatings is more difficult to summarize. However, most of the studies have focused on bloom occurring with CBS.
8.4.3.1 CBE
No studies relate problems of bloom occurring with CBE (except for synthesized CBE). However, CBE would be expected to have the same bloom behavior and mechanism as chocolate because of the similarity in TAG composition with CB.
cases, bloomed compound coatings made with CBS appear to still be in the b form, although this result is still in question and several recent studies suggest that the b polymorph is present in bloomed coatings. Furthermore, addition of milk fat enhances bloom in compound coatings, whereas it delays storage bloom in chocolate. Another difference in storage bloom formation between chocolate and compound coatings is the effect of storage temperature. In chocolate, it is clear that storage at elevated temperatures and with larger temperature fluctuations promotes bloom formation. However, in coatings, storage bloom often seems to be promoted at temperatures slightly below room temperature (about 18 7C) and inhibited when storage temperatures are higher or fluctuating. For these reasons, the bloom mechanism for coatings is often considered to be different from that of chocolate. In situations where a polymorphic change is associated with bloom formation in compound coatings, the general outline of bloom formation shown in Fig. 9 should apply in this case as well. Essentially, the same processes can explain the evidence for such bloom in compound coatings, with the exception of the effects of milk fat and storage temperature. If storage bloom in compound coatings occurs without a polymorphic transformation, a different mechanism is needed to explain this type of bloom. Hypothetically, the www.ejlst.de
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re-crystallization of high-melting TAG could occur in the same polymorph as the bulk of the coating; however, in this case, growth of existing crystals would be favored over formation of new ones. Perhaps the existing b crystals at the surface simply get larger and this is sufficient to disrupt reflection and give the appearance of bloom. The visual appearance of bloom on compound coatings (larger, grainer spots) suggests that perhaps this is indeed what happens. Further work is needed to document whether bloom can occur in compound coatings without the necessity of the polymorphic transition. Regardless of whether bloom in compound coatings occurs either with or without a polymorphic transition, the effects of milk fat and storage temperature still need to be understood. Milk fat inhibits bloom in chocolate but promotes bloom in lauric-based coatings. Perhaps the differences in chain length and degree of saturation between CB and PKO can explain their different behavior with milk fat and thus, the different effects of milk fat on bloom formation. Interestingly, milk fat and CB form a eutectic solid at when milk fat content reaches about 30%, whereas milk fat and modified PKO do not. How this phase mixing between the fats influences bloom formation is still unknown. In chocolate, bloom is promoted at elevated temperatures, where SFC is reduced. However, in lauric-based coatings, bloom is often promoted at about 18 7C and occurs more slowly at both higher and lower temperatures (although it is unknown if this general observation applies in all cases). SFC curves are generally similar for modified PKO and CB, although coatings made with hydrogenated PKO tend to be the most prone to bloom and these fats have the largest difference in SFC with CB. Perhaps this difference in SFC profile is somehow related to likelihood of bloom formation. However, the effect of SFC of the fat on bloom formation in coatings is still largely unknown and further research is needed to address this question.
Storage bloom with polymorphic transition is characteristic of chocolate. However it can affect also CC like CBE, and some CBS (hydrogenated PKO). Storage bloom without polymorphic transition has only been observed for some compound coatings, although further work is needed verify that this is actually true. Many factors have been found to affect bloom in chocolates and compound coatings. Some tend to accelerate bloom formation, like oil migration from a coated center, the presence of incompatible fats and improper storage temperatures. Some factors tend to inhibit bloom formation, like the use of milk fat in chocolate and proper storage temperatures. Despite the years of study of bloom, there are many aspects of this phenomenon that have still eluded a complete understanding.
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