influence of lipid composition, solid fat content and...

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Influence of Lipid Composition, Solid Fat Content and Temperature on Hardness of Margarines Zhili Liang 1 , Lin Li 1, 2 , Zhenbo Xu 1 , Bing Li 1+ 1 College of Light Industry and Food Science, South China University of Technology, Guangzhou 510640, China 2 Dongguan University of Technology, Dongguan 523808, China Abstract: By studying the lipid composition, crystallization behavior on hardness of margarines at different temperatures, the results generally show that there is no linear correlation between the hardness and temperature, which is different from the customary view. On the basis of these results, the reasons of hardness change are discussed, including triacylglycerol (TAG) composition, solid fat content (SFC), the experimental results reveal that the temperature influences these factors. Hardness is controlled not solely by any one of the lipid composition, solid fat content, it is the result of combined effects of lipid composition, solid fat content. Keywords: margarines, hardness, solid fat content 1. Introduction Margarine was invented by Me`ge Mourie`s in 1896 to meet the lack of cream resulting from the population increasing [1]. The original margarine was imitation products of natural cream, not only in taste, but also in raw materials which were tallow. With the oil refining technology improving, vegetable oil replaces animal oil in margarine production. Margarine are normally produced by vegetable oil undergone hydrogenation or fractionation or chemical transesterification or a combination of these methods which offer the possibility of changing the physical and chemical characteristics of lipids [2]. Hydrogenation allows the conversion of liquid oils into semisolid fats. These hydrogenated fats are characterized by altered melting and textural characteristics and a higher oxidative stability. Fractionation is a fully reversible modification and basically a thermo-mechanical separation process. It allows for different fractions, which will also alter the textural characteristics. Among the vegetable oils, palm oil has been widely applied in margarines due to its several advantageous properties, such as high productivity, low price, high thermal-oxidative stability and plasticity at room temperature [3]. The aim of this work was to compare two typical commercial margarines which respectively were produced by hydrogenated vegetable oil (denoted by A) and fractionated palm oil (denoted by B) in terms of lipid composition and SFC, so as to evaluate the relative effects of various factors on margarine hardness. 2. Materials and Methods 2.1. Materials A: Non-dairy whipped topping (slip melting point (SMP)5.1°C, acid value (AV) 0.34 and iodine value (IV) 0.76 g I/100 g; B: shortening (SMP47.4°C, AV 0.18 and IV 42.66 g I/100 g). Oil A was provided by Goldem Diamond Food Industrial Co., Ltd. (Guangzhou, China). B was purchased from PT Salim Ivomas + Corresponding author. Tel.: + 86-20-87113252; fax: +86-20-87113252. E-mail address: [email protected] 2014 3 rd International Conference on Nutrition and Food Sciences IPCBEE vol. 71 (2014) © (2014) IACSIT Press, Singapore DOI: 10.7763/IPCBEE. 2014. V71. 18 87

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Page 1: Influence of Lipid Composition, Solid Fat Content and ...ipcbee.com/vol71/018-ICNFS2014-A1031.pdf · Following the AOCS Official Method Cd 16b-93 [4], ... There is a direct correspondence

Influence of Lipid Composition, Solid Fat Content and Temperature

on Hardness of Margarines

Zhili Liang1, Lin Li

1, 2, Zhenbo Xu

1, Bing Li

1+

1 College of Light Industry and Food Science, South China University of Technology, Guangzhou 510640,

China 2 Dongguan University of Technology, Dongguan 523808, China

Abstract: By studying the lipid composition, crystallization behavior on hardness of margarines at

different temperatures, the results generally show that there is no linear correlation between the hardness and

temperature, which is different from the customary view. On the basis of these results, the reasons of

hardness change are discussed, including triacylglycerol (TAG) composition, solid fat content (SFC), the

experimental results reveal that the temperature influences these factors. Hardness is controlled not solely by

any one of the lipid composition, solid fat content, it is the result of combined effects of lipid composition,

solid fat content.

Keywords: margarines, hardness, solid fat content

1. Introduction

Margarine was invented by Me`ge Mourie`s in 1896 to meet the lack of cream resulting from the

population increasing [1]. The original margarine was imitation products of natural cream, not only in taste,

but also in raw materials which were tallow. With the oil refining technology improving, vegetable oil

replaces animal oil in margarine production. Margarine are normally produced by vegetable oil undergone

hydrogenation or fractionation or chemical transesterification or a combination of these methods which offer

the possibility of changing the physical and chemical characteristics of lipids [2]. Hydrogenation allows the

conversion of liquid oils into semisolid fats. These hydrogenated fats are characterized by altered melting

and textural characteristics and a higher oxidative stability. Fractionation is a fully reversible modification

and basically a thermo-mechanical separation process. It allows for different fractions, which will also alter

the textural characteristics. Among the vegetable oils, palm oil has been widely applied in margarines due to

its several advantageous properties, such as high productivity, low price, high thermal-oxidative stability and

plasticity at room temperature [3].

The aim of this work was to compare two typical commercial margarines which respectively were

produced by hydrogenated vegetable oil (denoted by A) and fractionated palm oil (denoted by B) in terms of

lipid composition and SFC, so as to evaluate the relative effects of various factors on margarine hardness.

2. Materials and Methods

2.1. Materials

A: Non-dairy whipped topping (slip melting point (SMP)5.1°C, acid value (AV) 0.34 and iodine value

(IV) 0.76 g I/100 g; B: shortening (SMP47.4°C, AV 0.18 and IV 42.66 g I/100 g). Oil A was provided by

Goldem Diamond Food Industrial Co., Ltd. (Guangzhou, China). B was purchased from PT Salim Ivomas

+ Corresponding author. Tel.: + 86-20-87113252; fax: +86-20-87113252.

E-mail address: [email protected]

2014 3rd

International Conference on Nutrition and Food Sciences

IPCBEE vol. 71 (2014) © (2014) IACSIT Press, Singapore

DOI: 10.7763/IPCBEE. 2014. V71. 18

87

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Pratama (Indonesia). All other chemicals were either of analytical or high-performance liquid

chromatography (HPLC) grades.

2.2. Fatty Acid Composition Analysis

Fatty acid methyl esters (FAMEs) were prepared according to the AOCS Official Method Ce 2-66 [4],

and subsequently analyzed on a GC-14B gas chromatograph (GC) equipped with a fused-silica capillary

column (CP-Sil88, 100 m× 0.25 mm × 0.2 mm) and a flame ionization detector (Shimadzu, Tokyo, Japan).

The temperatures of the injection port and detector were both set at 250°C. The column was successively

heated to 50°C and held for 1 min, programmed at 8°C/min to 195°C and held for 2 min, then programmed

at 3°C/min to 250°C and held for 5 min. The fatty acid species was identified by using the retention time of

the FAME standard solution and quantified based on relative peak area

2.3. Triacylglycerol (TAG) Composition Analysis

The sample was melted completely and then dissolved in chloroform with the 0.5 mg/mL concentration

TAGs were separated by reversed-phase high-performance liquid chromatography (HPLC) using a

Symmetry C18 column (250 mm× 4.6 mm, particle size 5 μm) (Waters, Ireland) with A phase: Acetonitrile;

B phase: n-hexane/ isopropanol (4:5, v/v), A/B=50:50, the eluent at a flow rate of 1.0 mL/min and detected

with an sevaporative light scattering detector (ELSD). TAGs were identified by HPLC coupled to

atmospheric pressure chemical ionization mass spectrometry (HPLC/APCI-MS) using same HPLC

conditions as described above. A platform liquid chromatography-tandem mass spectrometry Analysis

(Bruker Daltonics Inc, USA) mass spectrometer (MS) equipped with an APCI interface was run at an APCI

source block temperature of 100°C, probe temperature of 400°C and an MS multiplier voltage of 700 V. The

measurement range was between m/z 200 and 1200 [5]. Quantitative determination of individual TAG in the

fat blends was made by using the HPLC results following the procedures of Chen et al. [6].

2.4. Textural Measurements

Textural measurements of oil were held at -20°C, -10°C, 0°C and 10°C, each for 24 h, respectively, and

then measured via constant speed penetration on an SMS TA.XT2i texturometer (Stable Micro Systems,

Surrey, UK) using a cone probe (P/6). The probe was set to penetrate the product at a constant speed of 2.0

mm/s to a distance of 10 mm. The maximum penetration force and the final penetration force were recorded.

Hardness was reported as the maximum penetration force (kg) based on triplicate measurements.

2.5. SFC Determination

Following the AOCS Official Method Cd 16b-93 [4], the SFC of the samples was determined on a

PC120 pulsed nuclear magnetic resonance (pNMR) spectrometer (Bluker, Karlsrube, Germany). The sample

was placed in the NMR tube and successively melted at 70°C for 30 min, tempered at 0°C for 90 min, and

then kept at the 0°C, 5°C, 10°C, 21.1°C, 26.7°C, 33.3°C, 40°C, 45°C, each temperature for 30 min before

measurement was recorded. Triplicate measurements were obtained.

3. Results

3.1. Hardness of Margarines

There is a direct correspondence between the temperature and hardness, which is considered

accustomedly, but the research result indicates it is not true. Figure 1 illustrates that hardness of A is 0.3499

kg at -20C, then promptly reduces to 0.0028 kg at -10C, next to 0.0030 kg at 0ºC and 0.0035 kg at 10ºC,

hardness of B decreases rapidly from 8.2922 kg at -20ºC to 1.1038 kg at -10ºC, then up to 1.7663 kg at 0ºC

and reduces to 1.6556 kg at 10ºC. In addition, both A and B, hardness has very dramatic changes from -20ºC

to -10ºC. Hardness of the A straight from 0.3499 kg to 0.0028 kg, hardness of B reduces from 8.2922 kg to

1.1038 kg. However, according to the SPSS statistic analysis, both A and B, there is not a significant

difference in hardness range from -10ºC to 10ºC. In other words, from -10ºC to 10ºC, the hardness of both A

and B remain constant.

3.2. Fatty Acid Composition

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Table I gives the major fatty acids composition of A and B. It shows that A mainly contains fatty acid

C14:0, C16:0 and C18:2, B mainly contains C16:0 and C18:0, the saturated fatty acid content of A and B all

more than 60%, but A is mainly dominated by short-chain fatty acids, long and medium chain fatty acids

takes up a large proportion in B.

3.3. TAG Composition

According to the fatty acid compositions of the triglycerides and the distribution of the fatty acids on the

individual triglyceride molecules, Wiederman divided TAGs into four component categories: trisaturated (S3)

TAGs; disaturated-monounsaturated(S2U); monosaturated-diunsaturated (SU2); and triunsaturated (U3) [7].

Fig. 1: Hardness of A and B at different temperature

Table I: Fatty acids composition of A and B C14:0 C16:0 C18:0 C18:1 C18:2 others

A(%) 39.39 31.32 6.36 5.29 16.20 1.44

B(%) 9.18 49.65 29.96 6.10 3.73 1.37

Table II: Main TAG species present in A and B TAG species A(%) B(%)

S3

MMP 8.43 6.06

PPP 5.44 20.44

PPS 1.42 2.15

S2U

PPL 9.91 1.29

PPO 6.72 31.73

PSO 3.45 4.65

SSO 1.67 0.47

SU2

PLL 1.93 1.77

PLO 21.98 8.76

POO 9.25 17.33

SOO 6.43 1.21

U3

OLL 0.85 0.11

OOL 6.79 1.32

OOO 15.71 2.72

(M, myristic ; L, linoleic ; P, palmitic ; O, oleic; S, stearic)

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As the Table II showed, comparing with A, B contains more S3 and S2U TAGs, the content of PPP is up

to 20.44%, the content of PPO is even as high as 31.73%. S3, S2U, SU2 and U3 TAGs have different

crystallization properties, the lower content of S3 TAGs and higher content of SU2 TAGs make margarine A

crystallize difficultly at body temperature or above. These results can explain why the hardness of A is more

lower than the hardness of B at the same temperature.

3.4. SFC

For the oil products with special purpose, SFC value is an important indicator to discriminate properties,

for example, margarine requires plasticity as much as possible at refrigerator temperature, in order to

maintain its shape and prevent separating out oil at 27~32°C in a few time [8].

At all temperature, SFC values of A are lower than B in Figure 2, with the temperature increasing, SFC

values of both A and B have reduced. According to the AOCS Official Method Cd 16b-93 [4], an SFC value

is determined by detecting the NMR signal from both liquid and solid components in the fat sample, or by

detecting the change in the liquid signal as it is displaced by solid.

Fig. 2: SFC value of A and B

4. Discussion

Environmental effects become even more important (than molecular effects) beyond the microscopic

world, where heat and mass transfer effects will strongly influence the formation of nanostructures,

microstructures, and eventually a network [9], [10]. Figure 1 shows that there is no linear correlation

between the hardness and temperature. According to Narine and Marangoni’s theory, rheology, mechanical

strength and sensory impression of fat are determined by many factors [11]. In Figure 1, from -20ºC to -10ºC,

the hardness of both A and B has very dramatic changes. However, from -10ºC to 10ºC, the hardness of both

A and B remains constant. These results may be due to diversification of molecules at the molecule level

such as lipid composition. Other more important reasons are that different temperatures may influence its

other molecules properties such as solid fat content, polymorphism and microstructure. Deman and

Blackman had made physical and textural evaluation of some shortenings and margarines, their results

showed that the fat crystal network played an important role in the textural properties of the product [12].

Consistency of fats depended on the number, size, and type of crystals [13], as well as on the proportion of

solids in the fat, viscosity of the liquid, treatment temperature, and mechanical working.

Table I shows that A is mainly dominated by short-chain fatty acids, long and medium chain fatty acids

take up a large proportion in B. At the same degree of unsaturation, the long chain fatty acids have higher

SMPs than short chain fatty, which can partial interpret why the SMPs of B higher than A. Besides, in

margarine and shortening, S3 and S2U type TAGs with high SMPs are the main sources of crystal backbone

that provide texture for margarines, thus B has higher hardness than A may be due to B contains more long

and medium chain fatty acids with high SMPs. Furthermore, this difference of fatty acid composition will

result in the complexity of triglycerides. As different triglycerides mixture, oil’s properties are closely related

to the constitution of triglycerides. In margarine and shortening, S3 and S2U type TAGs with high SMPs are

the main sources of crystal backbone that provide texture for margarines. Besides, S2U TAGs are solid at

room temperature and melt at body temperature. SU2 and U3 TAGs serve to promote liquidity and ease of 90

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handling at low temperatures [7]. Comparing with A, B contains more S3 and S2U TAGs. S3, S2U, SU2 and

U3 TAGs have different crystallization properties, the lower content of S3 TAGs and higher content of SU2

TAGs make margarine A crystallize difficultly at body temperature or above. These results can explain why

the hardness of B is much higher than hardness of A at the same temperature in Figure 1.

From the above discussion, an accurate conclusion can be reached that the hardness is the result of

combined effects of lipid composition, solid fat content and the microstructure of the network of crystalline

particles. At relatively low temperature, the crystal network is compact and stronger, thus it is a key factor to

determine the hardness. However, at relatively high temperature, when the crystal network is not strong, or

even disappeared, the crystal clusters and crystals which are characterized by SFC and polymorphism, they

play important roles in determining the hardness.

5. Conclusions

In this work, the results generally show that there is no linear correlation between the hardness and

temperature, which is different from the customary view. The result is due to the temperature influences the

properties of lipid composition, solid fat content. At relatively low temperature, the crystal network is

compact and stronger, thus it is a key factor to determine the hardness.

6. Acknowledgement

This work is supported by the National Natural Science of China (No. 31130042), the National Key

Technology R&D Program (No. 2012BAD37B01), the Fundamental Research Funds for the Central

Universities, SCUT (No. 2014ZB0006).

7. References

[1] Laia, O., Ghazalia, H., Cho, F., Chong, C., Physical and textural properties of an experimental table margarine

prepared from lipase-catalysed transesterified palm stearin: palm kernel olein mixture during storage. Food

Chemistry 2000, 71, 173-179.

[2] Zhang, H., Xu, X., Mu, H., Nilsson, J., et al., Lipozyme IM‐catalyzed interesterification for the production of

margarine fats in a 1 kg scale stirred tank reactor. European journal of lipid science and technology 2000, 102,

411-418.

[3] Hodate, Y., Ueno, S., Yano, J., Katsuragi, T., et al., Ultrasonic velocity measurement of crystallization rates of

palm oil in oil-water emulsions. Colloids and Surfaces A: Physicochemical and Engineering Aspects 1997, 128,

217-224.

[4] Firestone, D., American Oil Chemists' Society, Champaign 2004.

[5] Jakab, A., Héberger, K., Forgács, E., Comparative analysis of different plant oils by high-performance liquid

chromatography–atmospheric pressure chemical ionization mass spectrometry. Journal of Chromatography A

2002, 976, 255-263.

[6] Chen, C. W., Chong, C. L., Ghazali, H., Lai, O. M., Interpretation of triacylglycerol profiles of palm oil, palm

kernel oil and their binary blends. Food Chemistry 2007, 100, 178-191.

[7] Wiedermann, L. H., Margarine and margarine oil, formulation and control. Journal of the American Oil Chemists

Society 1978, 55, 823-829.

[8] Gander, K. F., Margarine oils, shortenings, and vanaspati. Journal of the American Oil Chemists Society 1976, 53,

417-420.

[9] Klein, R., Meakin, P., Universality in colloid aggregation. Nature 1989, 339.

[10] Halsey, T. C., Diffusion-limited aggregation: a model for pattern formation. Physics Today 2000, 53, 36-41.

[11] Narine, S. S., Marangoni, A. G., Microstructure. Fat crystal networks 2005, 179-254.

[12] Deman, L., Deman, J., Blackman, B., Physical and textural evaluation of some shortenings and margarines.

Journal of the American Oil Chemists Society 1989, 66, 128-132.

[13] Nawar, W. W. (Ed.), Lipids, Marcel Dekker, New York 1985.

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