AU6177899A - Apparatus for formation of fat crystals - Google Patents

Apparatus for formation of fat crystals Download PDF

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AU6177899A
AU6177899A AU61778/99A AU6177899A AU6177899A AU 6177899 A AU6177899 A AU 6177899A AU 61778/99 A AU61778/99 A AU 61778/99A AU 6177899 A AU6177899 A AU 6177899A AU 6177899 A AU6177899 A AU 6177899A
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Australia
Prior art keywords
fat
crystallization
trays
oil feedstock
melting point
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AU61778/99A
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AU725400B2 (en
Inventor
Kiyoyuki Higuchi
Yuji Kuwabara
Atsushi Taniguchi
Shin Yoneda
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Fuji Oil Co Ltd
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Fuji Oil Co Ltd
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Description

-1cc C.
AUSTRALIA
PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT: Fuji Oil Company, Limited ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.
INVENTION TITLE: "APPARATUS FOR FORMATION OF FAT CRYSTALS" The following statement is a full description of this invention, including the best method of performing it known to me: C C, Q:\OPER\AXD\2236502.DIV 30/11/99 P:\OPER\AXD\2236502.DIV -30/11/99 -1A- The present invention relates to an apparatus for formation of fat crystals by standing and a process for the dry fractionation of fats and oils, especially, laurin fats and oils.
Fats and oils having high SFI (solid fat index) are effectively utilized by fractionation thereof into high and low melting point fractions. In general, high melting point fractions are more costly than low melting point fractions. In 10 fact, for example, in case of palm kernel oil (PKO), since its high melting point fraction (PKS) is useful as a raw material for the production of a cocoa butter substitute (CBS) and the like, PKS is marketed at a higher price than a low melting point fraction (PKL) of PKO and PKL is even cheaper than PKO per se as a raw material for the fractionation. Then, for the fractionation of fats and oils having high SFI, in many cases, activities have been attempted to increase the yields of high melting point fractions as high as possible efficiently.
At present, a representative process for the fractionation of palm kernel oil employed in the Malay Peninsula region is the dry fractionation, that is, fraction- 2 ation of fats and oils without using any solvent, detergent or the like.
In the typical dry fractionation, PKO is pre-cooled to about 27*C and distributed into many trays, followed by allowing to stand at 18 to 210C for about 10 hours to crystallize wrapping up the resultant cakes containing fat crystals with a filter cloth and subjecting the wrapped cakes to filtration under pressure (with a hydraulic press) to separate solids from a liquid phase ("SPECIALTY FATS VERSUS 0 COCOA BUTTER" By Wong Soon, 1991). Hereinafter, this process is referred to as the conventional process.
In the conventional process, for increasing the yield of PKS, it is required to sufficiently carry out standing of pre-cooled PKO distributed into trays to increase the amount of fat crystals to be formed. On the other hand, this causes difficulties in filtration (separation of a liquid phase from solids) and, in order to recover fat crystals with good quality, it is necessary to press the cakes containing fat crystals under high pressure with a hydraulic press for a long period of time. However, there is a certain limit to an increase in the yield of PKS by this procedure. Then, the improvement of the conventional process is directed toward to solve problems caused by intensive labor type steps as described below rather than to increase in the yield of PKS.
3 That is, the conventional process has been widely employed because of its low costs of facilities. However, a large number of trays are used in the standing step for crystallization (it is said that a large number of trays as many as 10,000 to 20,000 are required for the facilities treating 100 ton of PKO per day). This step is very simple and trays are merely allowed to stand in a large room or space (to put trays on shelves). Then, un-uniform atmospheric temperatures of respective trays cannot be avoided and to 0 control crystallization temperatures and time are difficult, which results in the problem that quality of products is apt to be inconsistent. In addition, there is such a defect that the filter cloth is apt to be worn out due to high pressure.
Furthermore, when the steps from the standing to the 15 filtration under pressure are inspected in detail, various steps such as those for releasing the cakes containing fat crystals which are in the state of solid or semi-plastic from respective trays, wrapping them individually, transferring the wrapped cakes and then laying up them in a hydraulic press are required. However, these respective steps can hardly be automated and a great deal of labor is required. In fact, it is said that 70 to 80 persons are required for the facilities treating 100 ton of PKO per day. Therefore, from an economic viewpoint, the conventional process would no longer be P:\OPER\AXD\2236502.DIV 30/11199 -4realized except in such a region that considerably cheaper manpower is available.
If it were possible to transfer the cakes containing fat crystals after crystallization, an automatic filter press could be used instead of a hydraulic press because the slurry of cakes could be transferred into the filter press through a pipe line and is filtered by the filter press. When a filter press can be used, such intensive labor type steps as wrapping the cakes with a filter cloth and laying up it in hydraulic press can be ,oet eliminated. Then, some activities have been attempted to employ a filter press. However, even if the cakes after fully crystallization is crushed or smashed, a slurry having S-sufficient fluidity cannot be obtained and therefore the fatty material can hardly be transferred through a pipe line.
15 Accordingly, at present, the amount of fat crystals to be formed is compelled to be controlled to maintain fluidability of slurry after cruching. That is, activities for saving manpower is being attempted at the sacrifice of the yield of PKS.
The present invention advantageously provides an apparatus for carrying out an economic process for the dry fractionation of fats and oils which can save a great deal of manpower by employing a filter press without the sacrifice of the yield of
PKS.
P:\OPER\AXD\2236502. DIV 30/11/99 This advantage as well as other advantages of the present invention will become apparent from the following description.
The present inventors have studied intensively based on recognition that to employ a filter press in the step for separating solids from a liquid phase is indispensable to save manpower and to obtain consistent quality of fractionated products. As a result, it has been found that, by recycling a S. certain amount of a fractionated low melting point fraction obtained in the separation step and mixing it with a fat-and-oil i 10 feedstock, even if a sufficient amount of fat crystals are formed, a slurry of cakes containing the fat crystals and having good fluidity can be obtained and, surprisingly, the yields fluidability higher than that of the conventional process can be achieved. Thereby, it has been also found that a pre-cooling temperature can be lowered to about a crystallization temperature and the crystallization time can be extremely reduced. Thus, the present invention has been completed According to the present invention there is provided an apparatus for formation of fat crystals by standing which comprises a container, distribution pipes and crystallization trays arranged in parallel, said container being divided into plural compartments with vertical partitions each upper part of which has opening so that a fat-and-oil feedstock is fed into each compartment, said compartments communicating with each other at a certain height from the bottom of said container so that said fat-and-oil feedstock is uniformly fed into respective P:\OPER\AXD\2236502.DIV 30/11/99 -6compartments, and said distribution pipes being connected to the bottoms of respective compartments so that said fat-and-oil feedstock therein is distributed to said crystallization trays, respectively.
The apparatus may advantageously be used in a process for the dry fractionation of fats and oils which comprises allowing to stand a fat-and-oil feedstock having SFI at 200C of, at least, 15 to form fat crystals and to obtain cakes containing fat crystals and subjecting the slurry of cakes to separation of solids from a liquid phase, said fat-and-oil feedstock to be allowed to stand being pre-cooled to a temperature of, at the highest, 30C higher than that of a cooling medium to be used for the formation of fat crystals.
Fat-and-oil feedstock The fat-and-oil feedstock is that having a high SFI at 200C, especially, SFI at 200C of 15 or higher, preferably, 20 or higher, more preferably, 30 or higher. Examples thereof include laurin fats and oils and hydrogenated fats and oils. A typical example of laurin fats and oils is palm kernel oil (PKO). The fat-and-oil feedstock is preferably mixed with a low melting point fraction and the fractionated low melting point fraction obtained from the separation step can be recycled for this purpose. A preferred proportion of the low melting point fraction to be mixed is 30% by weight or higher, preferably, by weight or higher based on the total weight of the resulting mixture of the fats and oils feedstock and the low melting point fraction. When the mixing proportion is smaller than this range, the desired slurry as described hereinafter cannot be prepared and the desired advantages of the present invention are hardly expected. From a technical viewpoint, there is no upper limit of the mixing 7 proportion. However, when the mixing proportion is too large more than 70% by weight), it is undesirable because of an increase in a loading which accompanies an increase in costs of facilities.
A recycling technique of a liquid oil to a fat-andoil feedstock is disclosed by JP-A 60-108498. However, this technique relates to the effective production of a liquid oil from a fat-and-oil feedstock having a low SFI and completely different from the present invention where the yields of solid fats are improved.
Pre-cooling For preventing wintering, the fat-and-oil feedstock is normally kept in a melted state with warming in a tank, for example, at 40 0 C or higher in case of PKO. This is'pre-cooled 15 with a heat exchanger or the like. The pre-cooling can be carried out with any known heat exchanger to a temperature of, at the highest, 3C higher than, preferably 1°C higher than a temperature for the formation of fat crystals by standing (cooling medium temperature). More preferably, the precooling is carried out to a temperature of equal to or desirably, 1 0 C lower than the crystallization temperature, or lower. The pre-cooling is preferably carried out at a temperature of, at the lowest, 50C lower than the crystallization temperature, at which no clear crystallization is taken place, for a relatively short period of time.
8 For adjusting a pre-cooling temperature to the above-described temperature, in practice, recycling of a fractionated low melting point fraction is required. When the recycling is not carried out, a blockade of a heat exchanger is caused by growth of crystals with the lapse of continuous S-treatment because of a high concentration of crystallizable *0 components, which makes a reliable cooling operation diffi- :cult.
Allowing to stand for formation of fat crystals The pre-cooled fat-and-oil feedstock optionally mixed with a low melting point fraction is distributed into trays and allowed to stand to form fat crystals. The distribution into each tray is preferably carried out within a short period of time with uniform distribution of crystals.
*fl.
In case of distribution of a large amount of the pre-cooled fat-and-oil feedstock (or a mixture thereof with a low melting point fraction) within a short period, one of preferred methods is to divide the pre-cooled fat-and-oil feedstock in a large container into small portions with vertical partitions and to distribute the portions in parallel into crystallization trays arranged in a multi-stage shelf. More specifically, for example, a large container is divided into small spaces with vertical partitions which communicate with each other at a certain height from the bottom of the container to form several compartments. Each compartment has a upper 9 opening from which the pre-cooled fat-and-oil feedstock is distributed into the compartment. The fat-and-oil feedstock is poured into the large container and is over-flowed from the upper part of compartments to uniformly fill up respective compartments. Thus, the feedstock is uniformly divided into small portions. Then, the feedstock divided into small portions are fed into crystallization trays in parallel and simultaneously through distribution pipes connected to the bottoms of respective compartments (each distribution pipe is 1: 0 provided with a valve which can open and close in parallel .with other valves by a mechanical or electronic means). When one distribution pipe is used to distribute a large amount of
S
the pre-cooled feedstock or a mixture thereof with a low melting point fraction into plural trays one by one (the 4 conventional process has employed such method that a precooled fat-and-oil feedstock is distributed into a tray placed on an uppermost stage to overflow from the tray to other trays placed on lower stages one by one), this procedure is timeconsuming and crystallization is taken place during the distribution, which varies quality and, in extreme cases, makes the distribution difficult.
After completion of distribution, the formation of fat crystals is carried out by allowing the trays to stand with the aid of a cooling medium at 18 to 210C. When air adjusted to a certain constant temperature is ventilated from 10 the side of trays placed on a multi-stage shelf, in comparison of allowing to stand as such without any cooling medium, more constant and reliable crystallization can be carried out.
Although the cooling medium is not limited to air, when a liquid cooling medium is used, more precise temperature control is required because of its larger thermal conductivity. In addition, as described hereinafter, since the time requiring for formation of fat crystals can be reduced by pre- 9.
cooling and using a cooling medium, it is possible to carry out continuous crystallization by placing trays on a conveyer without any large-scale facilities.
The formation of fat crystals is carried out by allowing to stand the trays until the iodine value (IV) of a fractionated low melting point fraction (palm kernel olein) *9*e p S 15 reaches about 23 or higher in case of PKO. Even if the crystallization by standing is carried out until the IV reaches 25 or higher, the desired slurry can be prepared by subsequent crushing or smashing and therefore the high yield of PKS can be achieved. Normally, the time required for the crystallization by allowing to stand the trays can be reduced to 4 to 6 hours, while trays are generally allowed to stand for about 10 hours for crystallization in the conventional process. It is considered that this reduction of the time required for the crystallization is resulted from a synergistic effect of improvement in the emission efficiency of latent 11 heat of crystallization due to convection of a system which is facilitated by a higher content of liquid components of the system as well as formation of nuclei for crystallization in the early stage due to the low pre-cooling temperature.
Crushing or smashing After the crystallization, cakes containing fat crystals is taken out of the trays and passed through a crusher. The cakes passed through the crusher becomes a slurry having fluidity. Therefore, it can be transferred to the pressing step through a pipe line. The crushing or S S"smashing can be carried out by a per se known method such as, for example, that disclosed in JP-A 2-14290.
S
Pressing and separation of solids from liquid phase The separation of solids from a liquid phase can be
*SS*
S
carried out by a per se known method. As described above, the cakes containing fat crystals is in the form of a slurry, it can be transferred through a pipe line, which makes possible to utilize a filter press which is efficient and suitable for automation.
By this separation step, the fat-and-oil feedstock is fractionated into high and low melting point fraction. The yield of the high melting point fraction is higher than that of the conventional process and quality thereof is the same as or higher than that of the conventional process.
P:\OPER\AXD\2236502.DIV 30/11/99 -12- Since the low melting point fraction thus fractionated is recycled and mixed with the fat-and-oil feedstock, the amount to be treated is increased so much. However, the low melting point fraction is a liquid component and readily passes through a filter cloth. Then, it scarcely effects on the treating time.
The following Examples and Comparative Examples further illustrate the present invention but are not to be construed to limit the scope thereof. In the Examples and Comparative Examples, all the "percents" are by weight unless otherwise 10 stated.
Example 1 illustrates the case that does not recycle liquid phase. Examples 2 to 4 illustrate the cases that the continuous treatment that recycles the low melting point fraction became stationary state by using the mixture of PKO and a certain amount of PKL, a low melting point fraction.
Example 1 RBD-PKO (refined bleached deodorized palm kernel oil, SFI at 20 0 C: 39) heated at 40 0 C (75 liters) was placed in a jacketed pre-cooling tank and cooled with stirring to 21 0 C by passing through cold water at 14 0 C through the jacket. Then, it was distributed into stainless trays each of which was 100 cm in length x 150 cm in width x 8 cm in height in an amount corresponding to 50 mm deep. The trays were cooled by ventilating cold air at 21 0 C on both upper and bottom surfaces of respective trays at a rate of 3 m/sec for 4 hours. The solidified oil was crushed to prepare a slurry and pressed into a filter press having filtration chambers of 15 mm thick. The slurry was pressed at the maximum pressure of 30 kg/cm 2 13 for 30 minutes to separate solids from a liquid phase. Then, IV values of PKS and PKL were analyzed. As a result, the IV values were 6.98 and 22.7, respectively (see Table Since the yield was as low as 29.9, the same procedure was repeated except that the cooling was carried out for 6 hours. As a result, the yield was increased to 33.1. However, the slurry had less fluidity and, although the filter press was barely 0, used, the industrial scale production by using this procedure would be considered to be difficult.
10 Example 2 RBO-PKO (48.8 liters) heated to 40 0 C and PKL (26.6 liters) were mixed and placed in a jacketed pre-cooling tank and cold water at 14 0 C was passed through the jacket to cool to 21 0 C. Then, the mixture was worked up according to the 15 same procedure as that described in Example 1. The results are shown in Table 1.
Example 3 and Comparative Example 1 Difference in cooling temperatures was investigated.
Namely, RBO-PKO (37.5 liters) heated to 40 0 C and PKL (37.5 liters) were mixed and placed in a jacketed pre-cooling tank jacketed and cold water at 14 0 C was passed through the jacket to cool to 20 0 C, 22 0 C, 24 0 C or 27 0 C. Then, the mixture was worked up according to the same procedure as that described in Example 1. The IV values of the resultant PKS fractions were 6.52, 6.55, 6.51 and 7.52, respectively and the IV values 14 of the resultant PKL fractions were 25.6, 25.5, 25.2 and 24.6, respectively (see Table 1).
These results suggest that, when the pre-cooling temperature is lower, the crystallization time becomes shorter.
Example 4 According to the same procedure as that described in Example 1, the fractionation was carried out except that by weight of PKL was mixed with PKO. The results are 10 shown in Table 1. As a reference, the estimated values of the conventional process are also shown in Table 1.
a 15 Table 1 Iv Mixing Prepropor- cooltion of ing PKL end temp.
Crystallization time (hours)
IV
of
PKS
Yield of
PKS
IV
of
PKL
I.
9* 9*
U.
S
en.
U U U U 10 Ex. 1 it Ex. 2 Ex. 3 6.98 7.19 6.22 6.55 6.52 6.55 6.51 7.52 6.61 29.9 33.1 30.9 35.9 39.8 39.1 36.4 32.8 30.7 22.7 23.5 23.5 25.0 25.6 25.5 25.2 24.6 25.0 o 5
U
Comp.
Ex. 1 Ex. 4 6 1.5 Conven- 0 27 10 7.0- 32.0 23.0 tional As described hereinabove, a filter press can be employed in the dry fraction of fats and oils by recycling a low melting point fraction and lowering a pre-cooling temperature. Thereby, it is possible to save of manpower and to obtain products having consistent quality. In addition, it is possible to improve the yields of PKS more than that of the conventional process.

Claims (3)

1. An apparatus for formation of fat crystals by standing which comprises a container, distribution pipes and crystallization trays arranged in parallel, said container being divided into plural compartments with vertical partitions each upper part of which has opening so that a fat-and-oil feedstock is fed into each compartment, said compartments communicating with each other at a certain height from the bottom of said container so that said fat-and-oil feedstock is uniformly fed into respective compartments, and said distribution pipes being connected to the bottoms of respective compartments so that said fat-and-oil feedstock therein is distributed to said crystallization trays, respectively.
2. Apparatus according to claim 1 and substantially as herein described. 9
3. The steps, features, compositions and compounds disclosed herein or referred to or indicated in the specification and/or claims of this application, individually or collectively, and any and all combinations of any two or more of said steps or features. DATED this 30th day of NOVEMBER, 1999 FUJI OIL COMPANY, LIMITED by DAVIES COLLISON CAVE Patent Attorneys for the Applicant
AU61778/99A 1996-03-28 1999-11-30 Apparatus for formation of fat crystals Ceased AU725400B2 (en)

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JP08/73486 1996-03-28
AU61778/99A AU725400B2 (en) 1996-03-28 1999-11-30 Apparatus for formation of fat crystals

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AU16247/97A Division AU715431B2 (en) 1996-03-28 1997-03-13 Process for dry fractionation of fats and oils

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Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0749592B2 (en) * 1986-08-04 1995-05-31 不二製油株式会社 Dry fractionation of oily substances
GB8911819D0 (en) * 1989-05-23 1989-07-12 Unilever Plc Counter current dry fractional crystallization
DE4132892A1 (en) * 1991-10-04 1993-04-22 Krupp Maschinentechnik SUBSTANCE MIXING FACTIONING

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