NZ615224B2 - Process for obtaining a constituent from whey protein concentrate - Google Patents
Process for obtaining a constituent from whey protein concentrate Download PDFInfo
- Publication number
- NZ615224B2 NZ615224B2 NZ615224A NZ61522412A NZ615224B2 NZ 615224 B2 NZ615224 B2 NZ 615224B2 NZ 615224 A NZ615224 A NZ 615224A NZ 61522412 A NZ61522412 A NZ 61522412A NZ 615224 B2 NZ615224 B2 NZ 615224B2
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- New Zealand
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- substream
- fat
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- stream
- microfiltration
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Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; PREPARATION THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/14—Milk preparations; Milk powder or milk powder preparations in which the chemical composition of the milk is modified by non-chemical treatment
- A23C9/142—Milk preparations; Milk powder or milk powder preparations in which the chemical composition of the milk is modified by non-chemical treatment by dialysis, reverse osmosis or ultrafiltration
- A23C9/1425—Milk preparations; Milk powder or milk powder preparations in which the chemical composition of the milk is modified by non-chemical treatment by dialysis, reverse osmosis or ultrafiltration by ultrafiltration, microfiltration or diafiltration of whey, e.g. treatment of the UF permeate
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/20—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from milk, e.g. casein; from whey
- A23J1/205—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from milk, e.g. casein; from whey from whey, e.g. lactalbumine
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/54—Proteins
- A23V2250/542—Animal Protein
- A23V2250/5424—Dairy protein
- A23V2250/54252—Whey protein
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2300/00—Processes
- A23V2300/34—Membrane process
Abstract
process for obtaining a constituent, such as whey protein isolate, from whey protein concentrate by microfiltration. Retentate is fed to a microfiltration arrangement (4) where at a first stage (see 5.1, figures 2(a) & 2(b)) the retentate stream is separated into a first fat enriched substream (see 255, figure 2(b)) and a first fat depleted substream (see 256, figure 2(b)). The first fat depleted substream is then fed to a second stage (see 5.2, figures 2(a) & 2(b)) where the first fat depleted substream is further separated into a second fat enriched substream and a second fat depleted substream. A recirculated substream (see 14, figure 2(b)) is then fed from the second or both the first and second fat depleted substreams back to the microfiltration arrangement. The two stage separation process, followed by recirculation of the fat depleted retentate, advantageously enhances the quality and yield of the end constituent. e 255, figure 2(b)) and a first fat depleted substream (see 256, figure 2(b)). The first fat depleted substream is then fed to a second stage (see 5.2, figures 2(a) & 2(b)) where the first fat depleted substream is further separated into a second fat enriched substream and a second fat depleted substream. A recirculated substream (see 14, figure 2(b)) is then fed from the second or both the first and second fat depleted substreams back to the microfiltration arrangement. The two stage separation process, followed by recirculation of the fat depleted retentate, advantageously enhances the quality and yield of the end constituent.
Description
Process for Obtaining a Constituent from Whey Protein Concentrate
The invention relates to a process for obtaining a constituent from a whey protein
concentrate obtained as retentate from ultrafiltration of whey, wherein the whey protein
concentrate is supplied as a feed stream to a microfiltration arrangement, and from its
retentate stream, a reduced-fat substream is separated and at least partially recirculated
into the microfiltration arrangement.
Abbreviated, a whey protein concentrate, obtained as a retentate from an ultrafiltration
of whey in prior art processes of this type, is also called "WPC (Whey Protein
Concentrate). It also contains, in addition to a whey protein fraction that is higher than
that of whey, a fraction of residual fats from the whey. Increasing the protein
concentration is particularly desirable for nutritional purposes, while the fat fraction is
undesirable. For reducing this unwanted fat fraction, the whey protein concentrate is
subjected to microfiltration. In the permeate from this microfiltration, the fat fraction is
substantially reduced compared to that of the whey protein concentrate, so that, from this
permeate, a substantially reduced-fat, protein-enriched product can be obtained. In
microfiltration, however, a substantial fraction of protein is lost to the microfiltration
retentate, thereby reducing the total yield.
The invention is based on the objective of improving the total yield in a process of the
type mentioned in the preamble.
According to the invention, this objective is achieved in that, in a first stage, the
retentate stream is separated into a first fat-enriched substream and a first fat-depleted
substream, in a second stage, the first fat-depleted substream is separated into a second
fat-enriched substream and a second fat-depleted substream, and the recirculated
substream is fed from the first and the second fat-depleted substream.
During microfiltration, part of the constituents contained in the incoming whey protein
concentrate, in particular of the protein, passes into the retentate stream. As a result, the
protein fraction discharged in the permeate stream is reduced. In practice, the protein
yield in the permeate stream is in the range of 75 % to 80 % of the protein content
present in the incoming whey protein concentrate. As a result of the invention-based
recirculation of the reduced-fat substream separated from the retentate stream from
microfiltration, a significant increase of the protein yield in the permeate stream from
microfiltration is achieved and, nevertheless, the fat content in the permeate stream is
maintained at desired low values. In practice, this increase in yield is, for instance, in
the range from 5 % to 10 % of the protein fraction present in the incoming whey protein
concentrate. The values for the yield increase and suppression of the fat content depend
on the recirculation quantity. In particular, the process according to the invention can be
executed with satisfactory success if the amount of the recirculated substream is for
example in the range of 25 % to 75 % of the quantity of the separated reduced-fat fat
substream or the quantity of the retentate stream of microfiltration.
The residual fat content recirculated with the recirculated substream is retained by the
microfiltration membrane according to the degree of separation of the microfiltration
arrangement applicable to fat, hence according to the natural defatting degree of the
latter, so that only a corresponding small fraction of the residual fat content passes into
the permeate stream. The natural degree of defatting of microfiltration is in the range of
75 % to 80 %, for instance. Then the fraction passing into the permeate is reduced to a
value in the range of 20 % to 25% of the recirculated residual fat content.
However, the fat content of the microfiltration retentates of whey has about 8 to 15 times
the fat content of the whey per se. In view of these high values, the invention allows
large-scale economical production by executing preliminary defatting in the first stage.
Preferably, in this stage, the retentate, having a dry matter content of 10 % to 20 %, for
instance, is reduced to a dry matter content of 5 % to 7 %. For this purpose, as a diluent,
a reverse osmosis permeate that occurs in the overall process flow of a dairy operation
from a reverse osmosis process can, for instance, be used. This achieves a viscosity that
is beneficial for efficient skimming. Before the separation in a cream separator, warming
to 40 ̊C to 50 ̊C takes place. The separated first fat-depleted substream from the cream
separator is separated in the second stage by chemical-physical action. From the second
fat-depleted substream occurring during this stage, the recirculation to the microfiltration
arrangement is fed. From the first and the second fat-enriched substreams, a
phospholipid concentrate, and from it, a phospholipid powder can be obtained.
The invention expediently provides that, ahead of the separation of the second fat-
depleted substream, the pH of the substream fed into the second stage is adjusted, the
pH-adjusted substream is heated, and the bivalent metal ion concentration of the heated
substream is increased. The adjustment of the pH prior to heating and the increase in the
bivalent metal ion concentration after heating cause an aggregation of the residual fat
particles and thereby facilitate separation of the fat-depleted substream. Separation is
further enhanced in that advantageously the substream from separation, adjusted in its
pH-value and its bivalent metal ion concentration, is supplied via a temperature holding
line.
In practice, the dwell period on the temperature holding line is expediently two to ten
minutes. Moreover, the substream heating temperature is in the range from 50 ̊C to 65 ̊C.
The adjustment of the pH to a value in the range of 6.4 to 7.0 takes place by the addition
of alkali, such as potassium hydroxide solution or sodium hydroxide solution. The
increase in the bivalent metal ion concentration takes place by an addition of calcium
chloride. Preferably, the second fat-depleted substream is separated from the heated
substream using a plate separator. The plate separator can be designed as a two-phase
separator, also called clarifying separator or clarifier, the discharge stream of which, that
discharges the light phase, delivers the second fat-depleted substream. Alternatively, the
plate separator can be a three-phase separator, also called separating separator, the
discharge stream of which, that discharges the heavy phase, delivers the second fat-
depleted substream. This possibility offers the advantage of separating not yet
aggregated fat fractions as light phase and thereby of further increasing the quality of the
treated retentate.
The scope of the invention furthermore provides for the protein-enriched product to be
obtained from a retentate stream of further ultrafiltration, to which the permeate stream
from the microfiltration is fed as a feed stream. As a result of the further ultrafiltration,
the protein-enriched and reduced-fat permeate stream from microfiltration is further
fractionated and cleaned. The retentate stream from this further ultrafiltration delivers a
highly protein-enriched and substantially reduced-fat product, the protein content of
which is, for instance, near or above 90 % and the fat content of which is less than 1 %.
Abbreviated, this product is also referred to as WPI (whey protein isolates.)
In the following specification, the invention is exemplified with reference to the
drawings, the following being shown therein:
Figure 1 shows a block diagram of a process flow, in which the invention is applied,
Figures 2 (a) and 2 (b) show detailed representations of sections of Figure 1, and
Figures 3 (a) and 3 (b) show, in each case, one schematic for explaining the
separation effect in a clarifying separator and a separating separator respectively.
In Figure 1, a Block 1 symbolizes whey as the starting material of the represented
process flow. For explaining the mass balances that occur in this process flow, in Block
1, exemplary only, a total throughput of whey having a dry matter content (TM ) of
1,000 kg is assumed. The whey is conducted to an ultrafiltration stage 2, in which it is
fractionated into a permeate and a retentate. The permeate from this ultrafiltration, in
which, in particular, the lactose and minerals of the whey are enriched, is supplied to a
further application not presented in Figure 1.
In the retentate from ultrafiltration, the whey proteins are enriched. Moreover, the
retentate contains a residual fraction of whey fat. For this whey protein concentrate,
abbreviated also called "WPC", in Block 3, the WPC mass balance, calculated from the
mass balance indicated in Block 1 and based on practice-oriented assumptions, is
indicated, namely 320 kg of dry matter. Contained therein are 112 kg protein dry matter
and 8 kg fat dry matter.
The whey protein concentrate composed in such a way is supplied as a feed stream to a
microfiltration stage 4. During this microfiltration, most of the protein fraction of the
supplied whey protein concentrate passes into the permeate of the microfiltration stage
4. In contrast, the fat content of this permeate is substantially reduced.
A smaller portion of the protein fraction and a larger portion of the fat fraction pass into
the retentate from microfiltration. In a separation stage 5, from the retentate stream from
microfiltration stage 4, a reduced-fat substream is separated. A Block 6 symbolizes the
recirculation of a portion of this substream into the feed of microfiltration stage 4. The
size of this portion is indicated as 33 % in Block 6. In fact, the size of the portion can be
varied within a wide range, depending on the circumstances that exist in actual practice,
in order to set an optimal yield, e.g. in the range of 25 % to 75 % of the reduced-fat
substream separated in separation stage 5.
Using this recirculation, for the exemplary mass balance on which Figure 1 is based, in
the permeate from microfiltration stage 4, calculation results in a dry matter content of
96.99 kg for protein and of 0.97 kg for fat. If, instead, the process were allowed to run
without the recirculation, the permetate from microfiltration stage 4 would only contain
89.60 kg of protein dry matter with 0.4 kg of fat dry matter. This means an increase of
8.25 % in the protein yield. At the same time, the percentual fat content continues to
remain below a threshold value of 1 %, as desired for nutritional purposes.
In the overall process represented in Figure 1, the permeate from microfiltration stage 4
is additionally subjected to a post-treatment for the purpose of cleaning and further
fractionation. For this purpose, the permeate stream is supplied to an additional
ultrafiltration stage 7 as feed stream. Its retentate provides a directly usable protein-
enriched product having a protein content of 90 % and a fat content of 0.95 %.
Abbreviated, such a product is called "WPI" (whey protein isolate).
Figure 2 (a ) shows details of an embodiment of a first stage 5.1 of separation stage 5 of
Figure 1. In this stage 5.1 , in a process step 250, the dry matter content of the retentate
stream from microfiltration stage 4, supplied at a dry matter content of 10 % to 20 %, is
reduced to a dry matter content of 5 % to 7 %. This takes place for example via infeed
251 of water or permeate from a reverse osmosis process, which takes place at a
different location of the overall process flow of a dairy operation. In a subsequent
process step 252, the dry matter-reduced permeate is heated to 40 ̊C to 55 ̊C and
subsequently supplied to input 253 of a cream separator 254. Its separation principle is
explained in exemplary form based on Figure 3 (b).
In cream separator 254, the supplied pre-treated retentate stream is separated into a first
fat-enriched substream 255 and a first fat-depleted substream 256.
In Figure 2 (b), within an area bordered by a dashed line, an embodiment of a second
stage 5.2 of separation stage 5 of Figure 1 is illustrated in more detail. This
representation shows that the pH of the first fat-depleted substream 256, supplied from
the first stage 5.1, is increased to a value in the range of 6.4 to 7.0 by an addition of
alkali, such as potassium hydroxide and/or sodium hydroxide solution from a vessel 9.
The temperature of the substream ph-adjusted in this manner is, for instance while
passing through a plate heat exchanger 10, heated to a temperature value in the range
from 50 ̊C to 65 ̊C. The bivalent metal ion concentration of the substream heated in this
manner is increased by the addition of calcium chloride from a vessel 11. The
substream heated in this manner is subjected, while passing through a temperature
holding line 12, for instance, to a heat retention period of two to ten minutes.
Thereafter, from the substream that is kept hot, in a separator 13, a second fat-depleted
substream 14 is separated and recirculated into the infeed of microfiltration stage 4.
The plate separator can be a two-phase separator, which is also referred to as clarifying
separator, or a three-phase separator, also referred to as separating separator. The
operating principle of the first alternative is represented in Figure 3 (a), that of the
second alternative in Figure 3 (b).
In Figure 3 (a) two superimposed plates 100, 100' of the clarifying separator plate pack
that rotates on vertical axis of rotation 101 are schematically represented. The retentate
to be separated, being kept hot, is supplied axially from the top, in the direction of arrow
102 and then runs from the bottom, in the direction of arrow 103, into the plate gap
confined between the two plates 100, 100'. While passing through the plate gap, along
path 104, by the action of centrifugal force, the high-fat phase is separated off and runs
along path 105 to the plate 100 in Figure 3 (a). From there, along plate 100, it reaches
the bottom and is ultimately discharged from the lower end of the plate gap, either
continuously via nozzles or discontinuously by timed evacuations.
At the upper end of the plate gap, the light, low-fat phase 106 is discharged and
recirculated in substreams to microfiltration stage 4.
In the case of the separating separator, whose operating principle is schematically
illustrated in Figure 3 (b), the infeed also takes place along axis of rotation 201 of the
rotating plate pack, axially from the top in the direction of arrow 202. In the plates 200,
200' of the plate pack, superimposed openings are embodied, which form a riser.
Through this riser, the retentate, kept hot while running in vertically from the bottom up
along arrow 203 into the plate gap confined between the plates 200, 200'. Subject to the
action of centrifugal force, a fat-enriched phase is separated in the direction of upper
plate 200 of Figure 3 (b) and runs along its wall on a path 204, to the lower end of the
plate gap, where it is discharged either continuously via nozzles or discontinuously by
timed evacuations. Moreover, a fat-enriched phase is separated off in the direction of
the lower plate 200' in Figure 3 (b) and runs along its the wall on a path 205 to the upper
end of the plate gap. There, this fat-enriched light phase is discharged as continuous
stream 206. The remaining low-fat phase leaves the plate gap via the lower end of the
latter along path 207 as heavy phase and is discharged as a continuous stream 208,
which is recirculated in substreams to microfiltration stage 4.
In Figure 2 (b), separator 13 is illustrated as an example of such a separating separator.
The recirculated substream 14 in Figure 2 represents the low-fat phase of the separating
separator. The paths 204 and 205 of the high-fat or fat-enriched phase supply a second
fat-enriched substream 209. From there, these phases are supplied to further processing,
not illustrated, into a phospholipid concentrate, from which ultimately a phospholipid
powder is obtained. The first fat-enriched substream 255, separated off in the first stage
.1, is also supplied to this processing arrangement. Also not illustrated is the path of
the permeate from the additional ultrafiltration stage 7 and its further use.
List of Reference Characters
1 Block (Whey)
2 Ultrafiltration stage
3 Block
4 Microfiltration stage
Separation stage
.1 First stage
.2 Second stage
6 Recirculation
7 Additional ultrafiltration stage
9 Vessel
Plate heat exchanger
11 Vessel
12 Temperature holding line
13 Plate separator
14 Reduced-fat substream/second fat-depleted substream/recirculated substream
100, 100' Plate
101 Axis of rotation
102 Arrow
103 Arrow
104 Path
105 Path of the high-fat phase
106 Light low-fat phase
200, 200' Plate
201 Axis of rotation
202 Arrow
203 Arrow
204, Path of the high-fat phase
205 Path of the fat-enriched phase
206 Continuous stream
207 Path
208 Continuous stream
209 Second fat-enriched substream
250 Process step
251 Supply
252 Process step
253 Input
254 Cream separator
255 First fat-enriched substream
256 First fat-depleted substream
Claims (22)
1. Process for obtaining a constituent from a whey protein concentrate obtained as a retentate from ultrafiltration of whey, wherein the whey protein concentrate is supplied as a feed stream to a microfiltration arrangement and from a retentate stream of which a reduced-fat substream is separated and at least partially recirculated as a recirculated substream into the microfiltration arrangement, wherein, in a first stage, the retentate stream is separated into a first fat-enriched substream and a first fat-depleted substream, in a second stage, the first fat-depleted substream is separated into a second fat-enriched substream and a second fat-depleted substream and that the recirculated substream is fed from the second or from the first and the second fat-depleted substream.
2. Process according to Claim 1, characterized in that the dry matter content of the retentate stream is adjusted to 5 to 7 % ahead of the first stage.
3. Process according to Claim 2, characterized in that the adjustment of the dry matter content takes place by diluting the retentate stream.
4. Process according to Claim 3, characterized in that a permeate from reverse osmosis is used for the diluting.
5. Process according to anyone of Claims 2 to 4, characterized in that the dry matter- adjusted retentate stream is heated to 40 ̊C to 50 ̊C prior to its separation.
6. Process according to anyone of Claims 1 to 5, characterized in that, from the first and/or the second fat-enriched substream, a phospholipid concentrate is obtained.
7. Process according to Claim 6, characterized in that, from the phospholipid concentrate, a phospholipid powder is obtained.
8. Process according to anyone of Claims 1 to 7, characterized in that, from the permeate stream from microfiltration, a protein-enriched product is obtained.
9. Process according to anyone of Claims 1 to 8, characterized in that the quantity of the recirculated substream is in the range of 25 % to 75 % of the quantity of the separated substream.
10. Process according to anyone of Claims 1 to 9, characterized in that the residual fat content recirculated with the recirculated substream is reduced by microfiltration, in the permeate stream of the latter, to a fraction that corresponds to its natural degree of defatting.
11. Process according to Claim 10, characterized in that the natural degree of defatting of microfiltration is in the range of 75 % to 80 % and that the fraction of the recirculated residual fat content passing into its permeate is in the range of 20 % to 25 %.
12. Process according to anyone of Claims 1 to 11, characterized in that in the second stage, prior to separation, the pH of the substream supplied to it is adjusted, the pH- adjusted substream is heated and the bivalent metal ion concentration of the heated substream is increased.
13. Process according to Claim 12, characterized in that the heating temperature of the substream is in the range from 50 ̊C to 65 C. ̊
14. Process according to Claim 12 or 13, characterized in that the heated substream is passed through a temperature holding line.
15. Process according to anyone of Claims 12 to 14, characterized in that the adjustment of the pH takes place by the addition of an alkali.
16. Process according to anyone of Claims 12 to 15, characterized in that the adjustment of the pH to a value in the range of 6.4 to 7.0 takes place.
17. Process according to anyone of Claims 12 to 16, characterized in that the increase in the bivalent metal ion concentration takes place by an addition of calcium chloride.
18. Process according to anyone of Claims 12 to 17, characterized in that the reduced-fat substream is taken from a discharge stream of a plate separator, to which the heated retentate stream is supplied as feed stream.
19. Process according to Claim 18, characterized in that plate separator is a two-phase separator, the discharge stream of which that discharges the light phase supplies the reduced-fat substream.
20. Process according to Claim 18, characterized in that the plate separator is a three- phase separator, the discharge stream of which that discharges the heavy phase supplies the reduced-fat substream.
21. Process according to anyone of Claims 8 to 20, characterized in that the protein- enriched product obtained from the permeate stream from microfiltration is obtained from a retentate stream of further ultrafiltration, to which the permeate stream from microfiltration is supplied as a feed stream.
22. A process according to claim 1, substantially as herein described or exemplified.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11001863.7A EP2497368B1 (en) | 2011-03-07 | 2011-03-07 | Method for obtaining a protein-enriched product from a whey protein concentrate |
| EP11001863.7 | 2011-03-07 | ||
| PCT/EP2012/001013 WO2012119768A1 (en) | 2011-03-07 | 2012-03-07 | Process for obtaining a constituent from whey protein concentrate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ615224A NZ615224A (en) | 2015-04-24 |
| NZ615224B2 true NZ615224B2 (en) | 2015-07-28 |
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