Process for demineralizing a dairy protein composition, dairy protein composition that can be obtained by said process, and installation for implementing said process.

Abstract

The present invention relates to a process for manufacturing a demineralized milk protein composition (LPC2), comprising the following steps: (i) supplying a milk protein composition (LPC); (ii) electrodialyzing the milk protein composition (LPC) on an electrodialyzer (5, 200), comprising cell units (15, 215) comprising three compartments (20, 26, 30; 220, 226, 230), and configured to substitute at least one cation with at least one hydrogen ion H+ in the milk protein composition (LPC) to obtain a milk protein composition that is at least partially demineralized and acidified (LPC1); (iii) electrodialyzing the milk protein composition (LPC1) obtained in step (ii); (iv) recovering the demineralized milk protein composition (LPC2). Figure 1.

Description

Title of the invention: Process for demineralizing a dairy protein composition, dairy protein composition capable of being obtained by said process, and installation for carrying out said process. technical field

[0001] The present invention relates to a process for demineralizing a milk protein composition, as well as the milk protein composition that can be obtained by this process, in particular a demineralized whey.

[0002] The present invention also relates to an installation for implementing the process of demineralizing a dairy protein composition. Previous technique

[0003] A milk protein component can be whey. Whey, also called serum or milk solids, is the liquid portion resulting from the coagulation of milk. Two main types of whey are distinguished: those produced in an acidic environment for the production of caseins or fresh cheeses (acid whey); and those produced for the production of caseins using rennet and for pressed cooked or semi-cooked cheeses (sweet whey).

[0004] Whey is mainly composed of water, lactose, proteins, particularly whey proteins, and minerals. Whey can be processed by isolating the lactose on the one hand, and the proteins on the other. Whey proteins can also be used as an ingredient in the manufacture of infant formula. Demineralized whey, particularly the lactose, can be used in the manufacture of confectionery, cakes and ice cream, prepared meals, pastries, etc.

[0005] Wheys can be demineralized by undergoing a nanofiltration step, followed by electrodialysis or by passing over cation and anion exchange resins to achieve demineralization rates of 70 to 90%, or even higher.

[0006] However, ion exchange resins generate large volumes of saline regeneration effluents that are difficult and costly to treat.

[0007] In parallel, consumers are increasingly seeking ingredients from the food industry that retain their original natural properties, and therefore are not modified and / or denatured, or in any case, as little as possible. Furthermore, there is also a demand for demineralization processes for dairy products that limit, or even eliminate, the presence of exogenous mineral species. Ion exchange resins operate by exchanging mineral species in the The composition to be treated against exogenous mineral species. However, omitting one or more passes through ion-exchange resins complicates obtaining highly demineralized dairy protein compositions, for example, 70%, 80%, or 90% demineralized. Since the demineralization process shifts to other treatment systems, there is a risk that the membranes of these systems will become fouled more quickly due to the significant mineral load.

[0008] The present invention thus aims to propose an improved demineralization process for a milk protein composition, in particular without the use of ion exchange resins (anionic and / or cationic).

[0009] The present invention also aims to provide a method for demineralizing a dairy protein composition limiting the introduction of exogenous mineral compounds into the dairy protein composition. Description of the invention

[0010] The present invention overcomes the aforementioned problems in that it relates, according to a first aspect, to a process for manufacturing a demineralized milk protein composition (CPL2), comprising the following steps, in particular carried out in series: (i)- supply of a milk protein composition (CPL); (ii)- electrodialysis of the milk protein composition (MPC) on an electrodialyzer, comprising cellular units including, in particular, three compartments, and configured to substitute at least one cation with at least one hydrogen ion H+ in the milk protein composition (MPC) to obtain a milk protein composition at least partially demineralized and acidified (MPC1); (iii)- electrodialysis of the milk protein composition (CPL1) obtained in step (ü);

[0011] (iv)- recovery of demineralized milk protein composition (CPL2).

[0012] Generally, during electrodialysis, dissolved ionized species, mineral or organic, such as salts, acids, or bases, are transported across ionic membranes under the action of an electric current. An electrodialysis unit may comprise cationic membranes (permeable to cations) and / or anionic membranes (permeable to anions) arranged in parallel and alternately. Under the action of the electric field applied by means of an anode and a cathode, the ECMs block anions and allow cations to pass through, while the AEMs block cations and allow anions to pass through. This creates concentrating compartments (concentrates) and desalination compartments. This most common type of electrodialysis is an electrodialysis unit whose basic cell unit comprises two compartments.The cellular unit corresponds, at the smallest repeating pattern, to the operations of concentration and desalination (a cor compartment. (responding to a concentration or desalination). The solutions are renewed in the compartments by a circulation parallel to the plane of the membranes. The application of a current is ensured by two electrodes parallel to the plane of the membranes and placed at the ends of the electrodialyzer.

[0013] Advantageously, and in an original manner, the present invention includes the use of an electrodialyzer comprising three compartments for carrying out step (ii) configured to allow cation substitution. Thus, in addition to the desalination compartments (in which the ions disappear) and the concentration compartments (in which the ions accumulate), the electrodialyzer of step (ii) includes cation conversion compartments.

[0014] The milk protein composition (MPC) obtained in step ii) is thus depleted in cations, and therefore acidified (with a decrease in pH).

[0015] The second electrodialysis (iii) is performed on an electrodialyzer comprising cells each consisting of two compartments. A first compartment receives the milk protein composition to be treated (CPL1), and a second compartment receives water at the beginning of the electrodialysis (iii). The water will become charged with salts from the ions extracted from the milk protein composition (CPL1) to form a brine.

[0016] Electrodialysis (iii) allows for the further extraction of cations, and allows for the extraction of anions, not extracted by the first electrodialysis.

[0017] The demineralization obtained for the recovered milk protein composition (CPL2) is advanced, and can reach a demineralization rate greater than or equal to 70%, in particular greater than or equal to 75%, or 80% or even 85%, more particularly greater than or equal to 90%.

[0018] Advantageously, the process according to the invention does not generate regeneration effluents requiring treatment, consumes no, or very little depending on the various variants developed below, exogenous acid(s), and is therefore less polluting. This process can be described as partially eco-efficient.

[0019] The milk protein composition obtained in step ii) has an acidic pH, in particular less than or equal to the isoelectric point of the proteins (in particular serum) of the CPL of step i), in particular less than or equal to 6, preferably less than or equal to 4.

[0020] This arrangement promotes control of microbiological stability. Furthermore, the milk protein composition can then undergo heat treatment (in particular pasteurization) under temperature and duration conditions different from those applied in a non-acidic environment, which helps to limit protein denaturation. The milk proteins are therefore advantageously less degraded.

[0021] Preferably, the temperature of the milk protein composition in step ii) and / or step iii) is less than or equal to 40°C, in particular greater than 0°C.

[0022] The milk protein composition recovered in step iv) has a pH greater than or equal to 5, in particular greater than or equal to 6, more particularly greater than or equal to 6.2, notably less than or equal to 8.

[0023] Dairy protein composition

[0024] Preferably, the milk protein composition is selected from: a whey, such as sweet whey or acid whey or a mixture thereof; an ultrafiltration milk permeate; a microfiltration milk permeate (also referred to as ideal or native whey); a whey retentate or ultrafiltration permeate; a retentate or ultrafiltration permeate of a milk microfiltration permeate; or a mixture of these (List I).

[0025] All the dairy protein compositions listed in Schedule I are considered to be whey or whey derivatives.

[0026] In one embodiment, the milk protein composition (MPC) and / or sweet whey and / or acid whey and / or native whey is / are raw, that is to say that it / they has / have not undergone any operation aimed at reducing its mineral content.

[0027] Whey or milk protein composition (MPC), cited without specification, may thus be raw or partially demineralized.

[0028] Sweet whey is preferably obtained by chemical treatment of milk, in particular using rennet, allowing the recovery of caseins on the one hand and sweet whey on the other.

[0029] Acid whey is preferably obtained by acid treatment of milk, in particular using lactic acid and / or hydrochloric acid, allowing the recovery of caseins on the one hand, and acid whey on the other.

[0030] Milk protein composition (MPC), in particular crude or partially demineralized, and / or whey, in particular crude or partially demineralized, may be pre-concentrated in order to increase its dry extract, mechanically (for example by reverse osmosis or nanofiltration or a combination thereof) or thermally (for example by evaporation of water).

[0031] Milk protein composition (MPC), in particular crude or partially demineralized, and / or acid whey, in particular crude or partially demineralized, and / or sweet whey, in particular crude or partially demineralized, and / or milk microfiltration permeate, in particular crude or partially demineralized, has a dry extract greater than 0% and less than or equal to approximately 16%, in particular less than or equal to approximately 6%.

[0032] Milk protein composition (MPC), in particular crude or partially demineralized, and / or acid whey, in particular crude or partially demineralized, and / or sweet whey, in particular crude or partially demineralized, and / or milk microfiltration permeate, in particular crude or partially demineralized, may / can undergo a pre-concentration step, as defined above, in order to have a dry extract greater than or equal to approximately 8% and less than or equal to approximately 32%.

[0033] The milk protein composition according to the invention is liquid when used. It can be obtained by reconstituting a liquid solution from powder(s) and / or liquid(s), in particular chosen from list I above.

[0034] Preferably, the milk protein composition in step i) is partially demineralized. This arrangement allows for a reduction in the size of the three-compartment electrodialyzer in step ii), and / or the size of the two-compartment electrodialyzer in step iii), i.e., the active membrane surface area.

[0035] Preferably, the demineralization rate of the milk protein composition in step i) is greater than or equal to 30%.

[0036] Preferably, the demineralization rate of the milk protein composition in step i) is less than or equal to 70%, preferably less than or equal to 60%, for example less than or equal to 50%.

[0037] Preferably, the demineralization rate of the milk protein composition obtained / recovered in step iv) is greater than or equal to 70%, in particular may be greater than or equal to 80% (DM80) or 85% (DM85), or even greater than or equal to 90% (DM90).

[0038] In one embodiment, the milk protein composition has a dry extract by mass greater than 1%, preferably greater than or equal to 5%, and less than or equal to 10%. This is, for example, unconcentrated whey.

[0039] In another embodiment, the milk protein composition has a dry matter content by mass greater than or equal to 10% and less than or equal to 30%; preferably greater than or equal to 15% and less than or equal to 25%. For example, it is a whey concentrate. The dry matter concentration of the whey can be achieved by reverse osmosis, nanofiltration, or any other thermal concentration method.

[0040] In general, the milk protein composition can be derived from any dairy female.

[0041] Preferably, the milk protein composition is derived from milk selected from: cow's milk, goat's milk, sheep's milk, donkey's milk, buffalo's milk, mare's milk, or a mixture of the latter, more preferably selected from: cow's milk, goat's milk and sheep's milk or a mixture of the latter, in particular cow's milk.

[0042] The protein composition includes milk proteins, in particular whey proteins.

[0043] The milk protein composition (MPC), in particular whey, comprises whey proteins, and does not include caseins remaining in the solidified (coagulated) portion during milk processing and / or in the microfiltration retentate of the milk.

[0044] Preferably, sweet whey, in particular raw, or native whey, in particular raw, has one of the following properties, alone or in combination: - a pH between 5.8 and 6.5; - the ratio of the mass of lactose to the mass of dry extract is greater than or equal to 70%, in particular greater than or equal to 74%; - the ratio of the mass of total nitrogenous matter to the mass of dry extract is greater than or equal to 10%, in particular greater than or equal to 12%, in particular less than or equal to 30%; - the ratio of the mass of ash to the mass of dry extract is greater than or equal to 8%, but in particular less than or equal to 10%; and - the ratio of the mass of organic acids to the mass of dry extract is greater than or equal to 2%, in particular less than or equal to 5%.

[0045] Preferably, the acid whey, in particular crude, has one of the following properties, alone or in combination: - a pH less than or equal to 5, in particular less than or equal to 4.5; - the ratio of the mass of lactose to the mass of dry extract is greater than or equal to 55%, in particular less than or equal to 65%, in the case of whey from the manufacture of cheeses in an acidic environment; - the ratio of the mass of lactose to the mass of dry extract is greater than or equal to 70%, in particular less than or equal to 85%, in the case of whey from the manufacture in an acidic environment of caseins; - the ratio of the mass of total nitrogenous matter (TM) to the mass of dry extract is greater than or equal to 4%, in particular less than or equal to 12%; - the ratio of the mass of ash to the mass of dry extract is greater than or equal to 10%, in particular less than or equal to 15%; and - the ratio of the mass of organic acids to the mass of dry extract is greater than or equal to 10%, in particular less than or equal to 20%, in the case of whey from the manufacture of cheeses in a lactic acid environment; - the ratio of the mass of organic acids to the mass of dry extract is greater than or equal to 2%, in particular less than or equal to 5%, in the case of whey from the manufacture in an acidic medium of caseins.

[0046] In one embodiment, the ratio of the mass of lactose to the mass of the dry extract of the CPL (step i) is greater than or equal to 50%, or 60% or 70%.

[0047] In one embodiment, the ratio of the mass of the total nitrogenous matter to the mass of the dry extract of the CPL (step i) is greater than or equal to 5%, or 10%, in particular greater than or equal to 12%, in particular less than or equal to 30%.

[0048] Demineralization essentially consists of the total or partial removal of ash present in the protein composition of milk, particularly whey.

[0049] Definitions - Measurement methods

[0050] The mass percentage of ash (or dry mass fraction of ash), in particular of the milk protein composition (CPL, CPL1, CPL2), can be determined with the standardized method NF V04-208 October 1989, entitled "Milk- Determination of ash- Reference method", in particular implementing an incineration method at 525°C.

[0051] In this text, the terms dry matter by mass or total dry mass refer, for example, to the dry mass of the milk protein composition (CPL, CPL1, CPL2), obtained after evaporation of the water until a stable total dry mass is obtained, expressed as a percentage of the total mass of the milk protein composition, particularly at atmospheric pressure. The dry matter by mass can be determined using the standardized method ISO 6731: January 2011, "Milk, cream, and unsweetened condensed milk - Determination of dry matter (Reference method)."

[0052] In this text, lactose is understood to mean lactose as defined in the Codex Alimentarius, Codex Stan 212-1999: a natural constituent of milk normally obtained from whey, in particular with an anhydrous lactose content greater than or equal to 99% mass / mass on a dry basis.

[0053] The determination of the mass content of lactose or sugar (or dry mass fraction) can be carried out by high-performance liquid chromatography, in particular using the standard NF ISO 22662, dated November 2007.

[0054] The methods that can be used to quantify the cations and anions of milk (calcium, magnesium, sodium, potassium, phosphorus / phosphate, citrate) can be chosen from the following methods: molecular absorption spectrometry, titrimetric / complexometric method, electrochemical method, atomic spectrometry, capillary electrophoresis, ion chromatography / conductimetric detection, nuclear magnetic resonance for 31P, enzymatic method / UV detection.

[0055] The dry mass fraction of total nitrogenous matter (TNM) can be determined using the standard NF EN ISO 8968-1 dated May 2014 (Kjeldhal method).

[0056] The following standards can be used to determine the mass content: for example in chlorides: potentiometric titration method (NF ISO 21422, February 2019); for example in total phosphorus: molecular absorption spectrometry method (NF ISO 9874, April 2008); for example in calcium: titrimetric method (ISO 12081:2010 standard); for example in calcium, sodium, potassium and magnesium: atomic absorption spectrometric method (ISO 8070:2007 standard) or ion chromatography; for example in lactic acid / lactate via ISO 8069 standard dating from 2005.

[0057] In this text, CPL refers to the milk protein composition according to the invention.

[0058] Preferably, the milk protein composition (or LPC), in step i), has a conductivity greater than or equal to 1 mS / cm, more preferably greater than or equal to 3 mS / cm, preferably greater than or equal to 8 mS / cm, in particular greater than or equal to 10 mS / cm.

[0059] Preferably, the CPL, recovered in step iv), has a mass percentage of ash less than or equal to 2.5% relative to the dry extract, preferably less than or equal to 1.5% relative to the dry extract, more preferably less than or equal to 1% relative to the dry extract, preferably less than or equal to 0.60% relative to the dry extract.

[0060] Preferably, the milk protein composition includes the following cations: calcium, magnesium, sodium, potassium, which are in particular the cations targeted by the demineralization process according to the invention.

[0061] Preferably, the milk protein composition comprises the following anions: chloride, phosphate, sulfate, lactate, acetate, and citrate, which are in particular the anions targeted by the demineralization process according to the invention.

[0062] In one embodiment, monovalent cations and monovalent anions are extracted at least in part from the CPL during a preliminary demineralization step, before step i), comprising a nanofiltration or reverse osmosis step.

[0063] Advantageously, the process does not include an anionic substitution step carried out on an electrodialyzer comprising cells each comprising three compartments, in particular configured to substitute at least one anion by at least one hydroxyl ion OH in the milk protein composition, in particular CPL1.

[0064] Advantageously, the process does not include a substitution step, in particular exclusively, of anions carried out on an electrodialyzer.

[0065] Advantageously, the process does not include an anionic substitution step carried out on an electrodialyzer comprising cells comprising compartments receiving the milk protein composition CPL1, each of the compartments of which is delimited between two anionic membranes.

[0066] In one embodiment, the process includes adding at least one basic solution, in particular adding at least one solution comprising at least one basic salt, to the milk protein composition during step (iii), in particular during at least part of step (iii), and / or after step (iii).

[0067] In one embodiment, the basic solution is a sodium hydroxide (NaOH) solution or a potassium hydroxide solution, or a mixture of said solutions.

[0068] In one embodiment, the basic solution comprises at least 0.5%, preferably at least 1% or 3% or 5%, by mass of the base (e.g. NaOH and / or KOH) relative to its total mass (including water).

[0069] In a first embodiment, a basic solution is added to the milk protein composition after step (iii), and then the milk protein composition (MPC2) with its pH adjusted is recovered. This may involve standardization. The recovered MPC2 includes the ions, particularly the cations, of the added basic salts. Depending on the desired mineral profile, this MPC2 may be suitable for certain applications.

[0070] In a second embodiment, possibly in combination with the first embodiment, a basic solution comprising the milk protein composition CPL1 is added to the compartments of the electrodialyzer in step (iii). The pH increase is thus preferably carried out during electrodialysis (iii).

[0071] Advantageously, said at least one basic solution can be added continuously or sequentially, in particular until the desired pH and / or the target conductivity is obtained.

[0072] Advantageously, said at least one basic solution is food grade.

[0073] Advantageously, raising the pH during step iii), in particular so as to be greater than or equal to the pKa of at least one organic acid in the composition being treated, makes it possible to obtain the anionic form of the organic acid and thus to extract it through the anionic membranes in step iii). The mobility of the anions is improved, and their extraction is thus facilitated.

[0074] This addition can be carried out by stopping the electrodialyzer (iii) (i.e. off power), then adding the basic solution to the CPL1, then restarting the electrodialyzer; or concomitantly with the extraction of ions (i.e. under power).

[0075] Advantageously, the addition of the basic solution during step (iii) is carried out when the conductivity (mS / cm) of the treated milk protein composition is lowered by at least 50%, preferably at least 75%, compared to the conductivity of the milk protein composition in step (i).

[0076] In one variant, the addition of the basic solution is carried out during at least part of the step (iii) of electrodialysis concomitantly with the extraction of ions, in particular cations and anions.

[0077] In addition to improving the extraction of anions, the inventors have observed that this arrangement improves the extraction of divalent cations (Ca2+; Mg2+), particularly compared to a demineralization process involving a substitution, in particular exclusively, cationic on a three-compartment electrodialyzer (ESC), followed by a conventional ED, and a substitution, in particular exclusively, anionic on a three-compartment electrodialyzer (ESA).

[0078] Advantageously, the addition of the basic solution is carried out during, in particular at least part of step (iii) of electrodialysis, under the application of an electric field. The electric field is generated by the application of a voltage (Volts) between the electrodes, anode and cathode, of the electrodialyzer (iii).

[0079] In one embodiment, the addition of the basic solution to the milk protein composition is carried out when the milk protein composition has a conductivity less than or equal to 1 mS / cm, and preferably has a pH greater than or equal to 3.

[0080] Advantageously, the addition of the basic solution to the milk protein composition is carried out when the milk protein composition has a conductivity less than or equal to 0.5 mS / cm, and preferably has a pH greater than or equal to 4.

[0081] In one embodiment, after the addition of the basic solution, the milk protein composition has a pH greater than or equal to 4.5, preferably greater than or equal to 5.0.

[0082] In one embodiment, the recovered milk protein composition (CPL2) after step (iii) has a pH less than or equal to 6.

[0083] It is then possible to standardize the CPL2 by an additional addition of a basic solution if it is necessary to adjust the pH between 6 and 7.

[0084] In one embodiment, the recovered milk protein composition (CPL2) after step (iii) has a pH greater than or equal to 6 after step (iii). The concentration of the basic solution and its application time during step (iii) are adjusted to achieve this pH.

[0085] In one variant, the electrodialysis step (iii) includes the extraction of anions and cations.

[0086] In one variant, step (ii) is a substitution step exclusively of cations.

[0087] In one embodiment, the electrodialyzer of step (ii) comprises cells comprising (made up of) (each) three compartments, and the milk protein composition (MPC) circulates in delimited compartments (each) between two cationic membranes.

[0088] In one variant, the milk protein composition recovered in step (iv) (CPL2) comprises phosphate ions (H2PO4, HPO42, PO43) of which the mass of phosphorus is greater than or equal to 110 mg, preferably greater than or equal to 150 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2).

[0089] Advantageously, the recovered milk protein composition (CPL2) comprises phosphate ions (H2PO4, HPO42, PO43) of which the mass of phosphorus is less than or equal to 210 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2).

[0090] The mass of phosphate ions is calculated on the basis of phosphorus.

[0091] The ionic profile of the recovered CPL2 includes more phosphate ions than when the process includes, after step (ii), an electrodialysis step for the extraction of anions and cations followed by an exclusively anionic substitution electrodialysis step.

[0092] In one variant, the milk protein composition recovered in step (iv) (CPL2) includes sodium or potassium ions, the mass of which is greater than or equal to 20 mg, preferably greater than or equal to 30 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2).

[0093] In one embodiment, the milk protein composition recovered in step (iv) (CPL2) comprises sodium or potassium ions, the mass of which is less than or equal to 80 mg, preferably less than or equal to 60 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2).

[0094] In one embodiment, the milk protein composition (CPL2) comprises sodium and / or potassium ions from said at least one added basic solution.

[0095] In one embodiment, the compartments of the electrodialyzer of step (ii) receiving the milk protein composition (MPC) are each delimited between two cationic membranes.

[0096] In one variant, the manufacturing process includes a treatment step (v) of at least a portion of the salt(s) selected from the following salts:

[0097] - the salt(s) obtained directly from the electrodialysis step ii), - the salt(s) indirectly derived from the electrodialysis step ii), - the salt(s) directly derived from the electrodialysis step iii), - the salt(s) indirectly derived from the electrodialysis step iii), - the salt(s) derived from a preliminary demineralization step carried out on the milk protein composition upstream of step i), - a mixture of the latter, Said processing step (v) being configured to produce one or more acidic salt(s) on the one hand, and / or one or more basic salt(s).

[0098] It is understood from the salt is directly from step ii) and / or iii) and / or i) that the latter has not undergone a step vi) or vii) defined below, in particular a nanofiltration step.

[0099] It is understood from the salt is indirectly derived from step ii) and / or iii) and / or i) that the latter has undergone a step vi) or vii) defined below, in particular a nanofiltration step.

[0100] The salt(s) used in the process according to the invention is / are preferably chosen from: a chloride of a monovalent cation; a chloride of a divalent cation; in particular sodium chloride, potassium chloride, and calcium chloride; a sulfate of a monovalent cation, a sulfate of a divalent cation; in particular sodium sulfate, potassium sulfate, and calcium sulfate; a phosphate of a monovalent cation, a phosphate of a divalent cation; in particular sodium phosphate, potassium phosphate, and calcium phosphate; and a mixture of the latter.

[0101] In one variant, the treatment step (v) consists of an electrodialysis step performed on a bipolar membrane electrodialyzer.

[0102] Advantageously, a bipolar membrane is composed of a cation exchange layer and an anion exchange layer separated by a hydrophilic junction.

[0103] In one embodiment, the bipolar membrane electrodialyzer(s), in step (v), comprises cell units comprising three compartments A, B and C, compartments A and B are supplied with water and compartment C is supplied with said salt(s), in particular compartment C is disposed between compartments A and B.

[0104] Preferably, the salt(s) is / are sodium chloride salt and / or potassium chloride salt (NaCl and / or KCl).

[0105] In one embodiment, the cellular units of the electrodialyzer in step v) each comprise a first compartment delimited between a bipolar membrane and an anionic membrane, a second compartment delimited between an anionic membrane and a cationic membrane, and a third compartment delimited between a cationic membrane and a bipolar membrane.

[0106] Preferably, the first compartment and the third compartment are supplied with water, and the second compartment, located between the first and third compartments, is supplied with salt(s).

[0107] Advantageously, step v), in particular the bipolar membrane electrodialysis step(s) v), makes it possible to generate an acid, in particular hydrochloric acid and / or sulfuric acid, and a base, in particular sodium hydroxide and / or potassium hydroxide, from the salt stream(s) from steps ii) and / or iii).

[0108] This arrangement allows the electrodialysis steps ii) and / or iii) to be carried out using acidic or basic salts derived from the milk protein composition itself. The process therefore eliminates, or at least significantly reduces, the introduction of exogenous mineral compounds.

[0109] The salt(s), in particular the sodium chloride salt, may also originate, in part, from the preliminary demineralization step(s) applied to the milk protein composition in step i), in particular from a nanofiltration step.

[0110] In one variant, at least part of the salt(s), in particular hydrochloric acid and / or sulfuric acid, obtained during the treatment step (v), is / are added to one of the three compartments of the electrodialyzer in step ii).

[0111] In one embodiment, the added basic solution comprises at least in part (is) the basic salt or basic salts, in particular sodium hydroxide and / or potassium hydroxide, obtained during the treatment step (v).

[0112] Advantageously, the base used is derived from the CPL itself, which avoids the addition of an exogenous base.

[0113] In one variant, the basic solution is derived at least in part from the recycling of an effluent from step ii) and / or step iii).

[0114] Effluent is understood to mean brine from ED (ii) or ED (iii).

[0115] Advantageously, recycling is carried out via step v).

[0116] In one variant, the milk protein composition is chosen from the list comprising: a whey, such as sweet whey or acid whey or a mixture thereof; an ultrafiltration permeate of milk, in particular skimmed milk; a microfiltration permeate of milk (also referred to as native or ideal whey); a whey retentate or ultrafiltration permeate; a retentate or ultrafiltration permeate of a milk microfiltration permeate; or a mixture of the latter, preferably a whey.

[0117] In one variant, the electrodialysis step ii) produces a mixture comprising at least one salt, in particular chloride, of a monovalent cation, such as a sodium chloride salt and / or a potassium chloride salt, and at least one salt, in particular chloride, of a divalent cation, such as a calcium chloride salt (CaCl2), and said mixture undergoes a separation step (vi), in particular a nanofiltration step.

[0118] Advantageously, the separation step (vi) allows the separation of the salt(s) of a monovalent cation, and of the salt(s) of a divalent cation.

[0119] In one variant, step (iii) includes electrodialysis of the at least partially demineralized and acidified milk protein composition (CPL1) obtained in step ii) on an electrodialyzer comprising cellular units comprising (consisting of) (each) two compartments. The electrodialyzer comprises several cells, for example at least five cells, preferably at least fifteen cells, and even more preferably at least 25 cells. In a first embodiment, the electrodialyzer comprises at least one cell unit comprising a first compartment delimited between a cationic membrane and an anionic membrane, and a second compartment delimited between an anionic membrane, in particular that of the first compartment, and a cationic membrane, in particular that of the first compartment.

[0120] Preferably, the first compartment is supplied with the partially demineralized and acidified milk protein composition (CPL1) obtained in step ii). Preferably, the second compartment is supplied with water.

[0121] This step advantageously allows the extraction of both anions and cations in CPL1.

[0122] This two-compartment electrodialysis step carried out after step ii) also makes it possible to achieve a removal rate of more than 80%, 85% or 90% in cations and anions, in particular with the addition of sodium hydroxide.

[0123] Step (ü) can be carried out before step viii) of heat treatment described below in this text.

[0124] In one variant, the electrodialysis step iii) produces a mixture comprising at least one salt of a monovalent anion and / or cation and / or at least one salt of a divalent anion and / or cation, in particular a sodium chloride (NaCl) salt and / or a sodium phosphate salt, and this mixture undergoes a separation step (vii), in particular a nanofiltration step.

[0125] Advantageously, the separation step (vii) allows the separation of the salt(s) of a monovalent anion, and of the salt(s) of a divalent anion.

[0126] Advantageously, steps vi) and / or vii) described in this text make it possible to complete the bipolar membrane electrodialysis(s), in particular if step ii) is carried out without permselective membranes, avoiding the precipitation of divalent cations, in particular calcium and / or magnesium, on the membranes, in particular on the cationic membranes of the bipolar electrodialysis of step v).

[0127] In one embodiment, the salt of a monovalent cation, in particular the chloride salt of a monovalent cation, preferably sodium chloride, collected at the end of the separation step (vi) and / or the separation step (vii), is fed to the electrodialysis step ii).

[0128] This provision applies in particular when step ii) is carried out with permselective membranes as defined below.

[0129] In one variant, the salt of a monovalent cation, in particular the chloride salt of a monovalent cation, preferably sodium or potassium chloride, collected at the end of the separation step (vi) and / or the separation step (vii) undergoes, at least in part, the treatment step (v).

[0130] This provision applies in particular when step (ii) is carried out without permselective membranes as defined below.

[0131] Advantageously, the treatment step (v) allows the production of a basic salt of said monovalent cation, in particular of sodium hydroxide or potassium hydroxide.

[0132] Advantageously, the basic salt from the treatment step (v) is used, in particular at least in part, as said at least a basic solution according to the invention.

[0133] In one variant, the electrodialyzer in step ii) comprises at least one monovalent cation permselective membrane.

[0134] Thus, the membrane, which is permselective to monovalent cations (or monovalent anions), is crossed only by monovalent cations (or monovalent anions), and is not crossed by anions (or cations), and cations (or anions) having a valence greater than 1, in particular divalent ones.

[0135] In one embodiment, the cellular units comprising three compartments of the electrodialyzer in step ii) comprise at least one cellular unit comprising, preferably each of the cellular units comprising: - a first compartment delimited between a membrane permselective to monovalent cations and a cationic membrane; - a second compartment delimited between two cationic membranes; - a third compartment delimited between a cationic membrane and a membrane permselective to monovalent cations.

[0136] In another embodiment, the cellular units comprising three compartments of the electrodialyzer in step ii) comprise at least one cellular unit comprising, preferably each of the cellular units comprising: - a first compartment delimited between an anionic membrane and a cationic membrane; - a second compartment delimited between two cationic membranes, and - a third compartment delimited between a cationic membrane and an anionic membrane.

[0137] The cation substitution step (ii) can thus be carried out using permselective or non-permselective membrane(s).

[0138] In a sub-variant (of the variants of step ii) above), the first compartment is supplied with at least one acid salt, preferably a hydrochloric acid salt, the second compartment is supplied with the milk protein composition of step i), and the third compartment is supplied with at least one chloride salt of a monovalent cation, preferably sodium, or with water.

[0139] In one variant, the process includes a heat treatment step (viii), carried out after step (ii), and preferably before step (iii).

[0140] Preferably, during this step (viii), the milk protein composition is at a temperature greater than or equal to 70°C and less than or equal to 110°C, for a time greater than or equal to 5 seconds and less than or equal to 10 minutes.

[0141] Advantageously, the heat treatment step is a pasteurization step.

[0142] The acidic environment of the milk protein composition promotes the elimination of germs, including those most difficult to destroy, for example spore-forming germs.

[0143] In one variant, the milk protein composition at step i) is whey, in particular from organic farming.

[0144] In one variant, the milk protein composition at step i) is a partially demineralized whey, in particular having undergone at least one step selected from: a nanofiltration step, a reverse osmosis step, an evaporation step, and a combination thereof.

[0145] These steps also allow the CPL to be concentrated, i.e., to increase its extract dry in bulk.

[0146] The present invention relates, according to a second aspect, to a demineralized milk protein composition that can be obtained according to any one of the variant embodiments / embodyments with reference to the first aspect of the invention.

[0147] In one variant, said milk protein composition comprises phosphate ions (H2PO4, HPO42, PO43) of which the mass of phosphorus is greater than or equal to 110 mg, preferably greater than or equal to 150 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2), and comprises sodium or potassium ions, of which the mass is greater than or equal to 20 mg, preferably greater than or equal to 30 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2), preferably the sodium and / or potassium ions are at least partly recycled and / or exogenous.

[0148] Advantageously, said milk protein composition comprises phosphate ions (H2PO4, HPO42, PO43) of which the mass of phosphorus is less than or equal to 210 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2), and comprises sodium or potassium ions, of which the mass is less than or equal to 80 mg, preferably less than or equal to 60 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2).

[0149] Preferably, the sodium and / or potassium ions are derived at least from the added basic solution, in particular from the basic salt recycled in step (v).

[0150] Preferably, the sodium and / or potassium ions are at least partly recycled ions from said demineralized milk protein composition.

[0151] Preferably, the sodium and / or potassium ions are at least partly exogenous ions to said demineralized milk protein composition.

[0152] Recycled ions are understood to mean ions extracted from the milk protein composition and added back to it.

[0153] Exogenous ions are understood to mean ions not derived from the milk protein composition.

[0154] The rate of demineralization of the milk protein composition is greater than or equal to 80%, or 85% or 90%.

[0155] The present invention relates, according to a third aspect, to an installation for implementing the process according to any one of the embodiments / modes of embodiment according to a first and / or a second aspect(s) of the invention, comprising:

[0156] a) a first electrodialyzer comprising a first inlet for receiving a milk protein composition (MPC), said electrodialyzer comprising cellular units comprising (each consisting of) three compartments, and configured to substitute at least one cation with at least one hydrogen ion H+ in the com milk protein position (CPL), and a first output for a milk protein composition at least partially demineralized and acidified (CPL1);

[0157] b) a second electrodialyzer comprising a first inlet for receiving the milk protein composition (CPL1) obtained in step (ii), and a first outlet for the milk protein composition (CPL2).

[0158] The first electrodialyzer enables the execution of step (ii) and the second electrodialyzer enables the execution of step (iii).

[0159] The first electrodialyzer and / or the second electrodialyzer may include any of the variants / embodyments described above with reference to the first aspect of the invention, in particular concerning the electrodialyzers of steps (ii) and (iii).

[0160] In one variant, the installation comprises:

[0161] c) a device comprising a basic solution and configured to be in fluidic communication for a given time with the compartments of the second electrodialyzer intended to receive the milk protein composition (CPL1), preferably under the application of an electric field.

[0162] Advantageously, the device supplies said at least one basic solution to the compartments of the second electrodialyzer receiving CPL1 concomitantly with the extraction of anions and cations from CPL1 for a determined time.

[0163] In one embodiment, the first electrodialyzer includes a second inlet for receiving at least one acid salt, in particular a hydrochloric acid salt and / or a sulfuric acid salt, and a third inlet for receiving water or a salt, in particular a chloride salt of a monovalent cation (NaCl and / or KCl).

[0164] In one variant, the installation includes a treatment unit (v), in particular an electrodialyzer comprising cells comprising three compartments and bipolar membranes.

[0165] In one variant, said treatment unit (v) comprises a first inlet receiving water and a second inlet receiving a salt of a monovalent cation (NaCl, KCl), and a first outlet for an acidic salt (HCl), and a second outlet for a basic salt (NaOH and / or KOH).

[0166] In one embodiment, said basic salt is supplied to said device c) comprising a basic solution.

[0167] In one embodiment, the acid salt is fed to the second inlet of the first electrodialyzer a).

[0168] In one variant, the installation includes a salt separation unit, in particular for carrying out step (vi) or step (vii).

[0169] Preferably, the separation unit (vi) or (vii) comprises a first inlet receiving at least one salt of a monovalent anion and / or cation and / or at least one salt of a divalent union and / or cation, in particular a sodium chloride (NaCl) salt and / or a sodium phosphate salt, and: - a first output for the salt(s) of a monovalent cation and a second output for the salt(s) of a divalent cation, when the first input receives salts of monovalent and divalent cations; or - a first output for the salt(s) of a monovalent anion and a second output for the salt(s) of a divalent anion, when the first input receives salts of monovalent and divalent anions.

[0170] Preferably, the separation unit (vi) or (vii) is a nanofiltration unit. Brief description of the drawings

[0171] The invention will be better understood upon reading the following description of embodiments of the invention given by way of non-limiting examples, with reference to the accompanying drawings, in which:

[0172] [Fig.1] [Fig.1] schematically represents the different stages of a first example of a manufacturing process for a demineralized dairy protein composition;

[0173] [Fig.2] Fig.2 schematically represents an example of the treatment step v) according to the invention, in particular a cell unit of the bipolar membrane electrodialyzer implemented in the first and second process examples shown in Figures 1 and 3; and

[0174] [Fig.3] [Fig.3] schematically represents the different stages of a second example of a manufacturing process for a demineralized dairy protein composition.

[0175] Description of embodiments by way of non-limiting

[0176] The first example of a process for manufacturing a demineralized milk protein composition shown in [Fig. 1] comprises two electrodialyzers (ED) 5 and 10. The cell units 15 of ED 5 have three compartments. The cell units 35 of ED 10 have two compartments. Only one cell unit 15 of electrodialyzer 5 is shown in [Fig. 1]. This cell unit 15 comprises a first compartment 20 delimited between a cationic permselective membrane 22 and a cationic membrane 24, a second compartment 26 delimited between the cationic membrane 24 and the cationic membrane 28, and a third compartment 30 delimited between the cationic membrane 28 and the cationic permselective membrane 32. Only one cell unit 35 of electrodialyzer 10 is shown in [Fig. 1].This cellular unit 35 comprises a first compartment 39 delimited between a cationic membrane 37 and an anionic membrane 41, a second compartment 43 delimited between the anionic membrane 41 and a cationic membrane 45.

[0177] The cation-selective permselective membranes 22 and 32 can only be traversed by monovalent cations. The electrodialyzers 5 and 10 each comprise a cathode (80,88) and an anode (78,90) generating a current through the conductive solutions passing through the compartments of cell units 15 and 35.

[0178] The process may also include a first nanofiltration device 50 for carrying out step vi) and / or a second nanofiltration device 60 for carrying out step vii), and / or a bipolar membrane electrodialyzer 70 for carrying out step v) according to the invention, particularly detailed in [Fig. 2]. This first example of the process also includes a heat treatment unit 75 for carrying out the heat treatment step viii), in particular pasteurization.

[0179] In operation, a milk protein composition (MPC), in particular whey, optionally demineralized to at least 30%, is supplied in step (i) and then fed into the second compartment 26 of the electrodialyzer 5 for the performance of step (ii). At the same time, acidified salt, in particular a hydrochloric acid solution, is fed into the first compartment 20, and brine, in particular a sodium chloride salt, is fed into the third compartment 30. H+ ions cross the cationic membrane 24 and are replaced by Na+ ions from the third compartment 30, which cross the permselective membrane 32 or 22 under the effect of the electric field. Mono- and / or divalent cations, in particular Na+ and Ca2+ ions, cross the cationic membrane 28 under the effect of the electric field, towards the cathode 80, and are replaced by H+ ions from the first compartment 20.The milk protein composition obtained CPL1 in step ii) is thus partially demineralized, the cations having been replaced by H+, and acidified. The pH of CPL1 is less than or equal to 4. The third compartment 30 comprises a mixture of chloride salts, notably a calcium chloride salt (CaCl2) and a sodium chloride salt (NaCl), derived from the milk protein composition CPL. Monovalent ions (e.g., Na+; K+) thus pass through the cation-selective permselective membrane 22 or 32 and supply the first compartment 20, while divalent ions (e.g., Ca2+) remain in the third compartment 30.

[0180] The acidified milk protein composition CPL1 can undergo heat treatment in step viii (heated to 90°C for a few minutes) to improve its bacteriological stability. Advantageously, since the CPL1 composition is acidified, the heat treatment conditions can be more advanced than usual and defined so that the proteins are not altered.

[0181] The mixture of salts from the third compartment 30 can undergo a nanofiltration step vi) on the nanofiltration unit 50 in order to increase the purity of the sodium chloride salt from the third compartment 30 by retaining divalent salts, such as calcium chloride CaCl2. The purified sodium chloride salt can thus advantageously be fed into the third compartment 30.

[0182] The CPL1 composition, in particular pasteurized, undergoes a second step of electrodialysis iü) on the electrodialyzer 10.

[0183] The first compartment 39 is supplied with heat-treated and acidified CPL1. The second compartment 43 receives water. The anions (chlorides, phosphates) pass through the anionic membrane 41 and are retained in the second compartment. The cations (sodium, magnesium) pass through the cationic membrane 37 and remain in the brine compartment. The recovered CPL2 composition is thus demineralized and deacidified.

[0184] In the second compartment 43, the mixture of sodium chloride and / or potassium chloride salts (NaCl, KCl) and phosphate salts, from CPL1, can undergo a step vii) of nanofiltration allowing to increase the purity of the sodium or potassium chloride salt by retention of phosphate ions.

[0185] The process according to the invention, and in this specific example the first example of a process, may advantageously also include a step v) of treating the sodium or potassium chloride salt on a three-compartment bipolar membrane electrodialysis unit 70 allowing the regeneration of the acid, mainly HCl, and the base, mainly sodium or potassium hydroxide, from:

[0186] - fluxes of the salt(s), in particular NaCl and / or KCl, from the first com section 20 of step ii) of cationic electrodialysis, and / or

[0187] - possibly NaCl and / or KCl from the pre-step(s) demineralization carried out upstream on the CPL composition of step i);

[0188] - and / or food grade NaCl and / or KC1;

[0189] - and / or NaCl and / or KC1 fluxes from step (vi) and / or step (vii).

[0190] Said pre-demineralization step preferably consists of a nano step filtration.

[0191] In a preferred embodiment, the recycled basic salt in step (v) is added to CPL1 in compartment 39, in particular during the extraction of anions and cations, i.e. under the effect of an electric field.

[0192] In another embodiment, the electrodialyzer 10 is stopped and then a basic salt is added to CPL1 in compartment 39, and then the electrodialyzer is restarted to continue demineralization.

[0193] In one embodiment, possibly combined with either of the two preceding embodiments, a basic solution is added after step (iii).

[0194] With the exception of the salt used at the start of step v), the acidic and basic salts used for the implementation of the electrodialysis steps ii) and iii) are derived from the milk protein composition CPL1, which avoids the introduction of exogenous mineral compounds.

[0195] Figure [Fig. 2] represents the electrodialyzer 70 and a cellular unit 105 thereof comprising a first compartment 110 delimited between a bipolar membrane 112 and an anionic membrane 114, a second compartment 116 delimited between the anionic membrane 114 and a cationic membrane 118, and a third compartment 120 delimited between the cationic membrane 118 and a bipolar membrane 122. The salt, in particular sodium or potassium chloride, is supplied to the second compartment 116. Chloride ions cross the anionic membrane 114 under the influence of the electric field towards the anode 125, while Na+ and K+ ions cross the cationic membrane under the influence of the electric field towards the cathode 127. This step (v) allows the regeneration of acidic and basic salts, in particular hydrochloric acid and sodium hydroxide, which can then be supplied, for the acidic salt, to the first compartment of cell unit 15 or 215 of step (ii), and / or for the basic salt, to the first compartment 39 or 239 of cell unit 35 or 235 of step iii) during the step of adding at least one basic solution according to the invention.

[0196] The second example of a process for manufacturing a demineralized milk protein composition shown in [Fig. 3] comprises two electrodialyzers 200 and 205. Electrodialyzer 200 comprises cell units 215, each comprising three compartments. Electrodialyzer 205 comprises cell units 235, each comprising two compartments. Only one cell unit 215 of electrodialyzer 200 is shown in [Fig. 3]. This cell unit 215 comprises a first compartment 220 delimited between an anionic membrane 222 and a cationic membrane 224, a second compartment 226 delimited between the cationic membrane 224 and the cationic membrane 228, and a third compartment 230 delimited between the cationic membrane 228 and the anionic membrane 232.

[0197] A single cell unit 235 of the electrodialyzer 205 is also shown in [Fig.3]. This cell unit 235 comprises a first compartment 239 delimited between a cationic membrane 237 and an anionic membrane 241, a second compartment 243 delimited between the anionic membrane 241 and a cationic membrane 249.

[0198] The electrodialyzers 200 and 205 each comprise an anode (278, 290) and a cathode (280, 288) generating a current through the conductive solutions passing through the compartments of the cell units 215 and 235. The process may also include a first nanofiltration device 250 for carrying out step vi), and / or a second nanofiltration device 260 for carrying out step vii), and / or a three-compartment bipolar membrane electrodialyzer 70, in particular detailed in [Fig. 2] for carrying out step v). In addition, the process may include a heat treatment unit 275 for carrying out the heat treatment step viii), in particular pasteurization.

[0199] During operation, a CPL milk protein composition, including demineralized whey at least 30%, is fed into the second compartment 226 of the electrodialyzer 200. Simultaneously, acidified salt, in particular a hydrochloric acid solution, is fed into the first compartment 220, and water is fed into the third compartment 230. Only H+ ions cross the cationic membrane 224 into the second compartment 226 towards the cathode 280, and chloride ions cross the anionic membrane 232 into the third compartment 230 towards the anode 278. In the second compartment 226, monovalent or divalent cations, such as Na+ and Ca2+, cross the cationic membrane 228 under the influence of the electric field towards the cathode 280, and are replaced by H+ ions from the first compartment 220. The milk protein composition obtained CPL1 in step ii) is thus partially demineralized, the cations having been replaced by H+ ions, and acidified. The pH of CPL1 is less than or equal to 4.The third compartment 230 contains a mixture of CaCl2 and NaCl from the milk protein composition CPL. Chloride ions from the first compartment 220 cross the anionic membrane 222 or 232 and supply the third compartment 230.

[0200] The acidified milk protein composition CPL1 preferably undergoes heat treatment in step viii), in particular a thermization step (heated to 90°C for a few minutes) to improve its bacteriological stability. Advantageously, since the CPL1 composition is acidified, the conditions of the heat treatment can be defined so that the proteins are not altered.

[0201] The mixture of salts from the third compartment 230 can undergo a step vi) of nanofiltration on the nanofiltration unit 250 in order to increase the purity of the sodium chloride salt from the third compartment 230 by extraction of divalent salts, such as calcium chloride CaCl2. This step can optionally be followed by a passage through a chelating resin to achieve the specification of 3-5 ppm at the inlet of step v).

[0202] The CPL1 composition, in particular thermized, undergoes a second electrodialysis step iii) on the electrodialyzer 205.

[0203] The first compartment 239 is supplied with heat-treated and acidified CPL1. The second compartment 243 receives water. The anions (chlorides, phosphates) pass through the anionic membrane 241 and are retained in the second compartment 243. The cations (sodium, magnesium) pass through the cationic membrane 237 and remain in the brine compartment (243). The CPL2 composition recovered in step iv) is thus demineralized and deacidified.

[0204] In the second compartment 243, the mixture of sodium chloride and / or potassium chloride salts (NaCl, KCl) and phosphate salts, from CPL1, can undergo a step vii) of nanofiltration allowing to increase the purity of the sodium chloride salt by retention of phosphate ions.

[0205] The method according to the invention, and in particular this second example of a method, may advantageously include also step v) of treatment of sodium or potassium chloride salt on a three-compartment bipolar membrane electrodialysis unit, in particular the electrodialyzer 70 shown in [Fig.2] and described above, allowing regeneration of the acid, mainly HCl, and the base, mainly sodium or potassium hydroxide, from:

[0206] - flows of salts, in particular NaCl and / or KCl, from the pre-step(s) demineralization carried out upstream on the CPL composition of step i);

[0207] - and / or food grade NaCl and / or KC1;

[0208] - and / or NaCl and / or KC1 fluxes from step (vi) and / or step (vii).

[0209] Said pre-demineralization step preferably consists of a nano step filtration.

[0210] In a preferred embodiment, the recycled basic salt in step (v) is added to CPL1 in compartment 239, in particular during the extraction of anions and cations, i.e. under the effect of an electric field.

[0211] In another embodiment, the electrodialyzer 205 is stopped and then a basic salt is added to CPL1 in compartment 239, and then the electrodialyzer 205 is restarted to continue demineralization.

[0212] In one embodiment, possibly combined with either of the two preceding embodiments, a basic solution is added after step (iii).

[0213] With the exception of the salt used at the start of step v), the acidic and basic salts used for the implementation of the electrodialysis steps ii) and iii) are derived from the milk protein composition CPL1, which avoids the introduction of exogenous mineral compounds.

[0214] The second example of a process differs from the first example by the use of permselective membranes in step (ii).

[0215] Step ii) of cationic substitution can be carried out interchangeably on electrodialyzer 5 ([Fig.1]) or 200 ([Fig.3]).

[0216] For the tests described below, a milk protein composition, CPL, was prepared by mixing a dispersion of 16% dry weight sweet whey powder (raw) in demineralized water. The dispersion was mechanically stirred until a homogeneous mixture was obtained. CPL thus has the following parameters: dry matter mass percentage: 15.9% (powder mass / total mass); pH = 5.95; initial conductivity: 10.95 mS / cm; ash mass percentage: 8.1%; lactose mass percentage: 73.5%; cation mass percentage (in particular Na, NH4, K, Ca, Mg): 3.79%; anion mass percentage (in particular Cl, NO3, PO4, SO4): 3.64%; The different mass ratios (with the exception of that in dry matter) are calculated by relating the total mass of one or more compound(s) to the total mass of the dry matter.

[0217] 1- Cationic substitution on the electrodialyzer 200 ([Fig.3]) The electrodialyzer 200 comprises, for example, 5 to 15 cells 215. The first compartment 220 is supplied with an HCl solution having a conductivity greater than or equal to 100 mS / cm, in particular greater than or equal to 150 mS / cm. The second compartment 226 is supplied by PLC as exemplified above. The third compartment is initially supplied with a NaCl solution having a conductivity less than or equal to 50 mS / cm, in particular less than or equal to 25 mS / cm, in this specific example, less than or equal to 15 mS / cm. A current (I) greater than or equal to 1 ampere, in particular less than or equal to 2 amperes, is applied to the electrodialyzer 200, and the voltage is preferably left free. During electrodialysis (ii), the conductivity of CPL decreases, indicating its demineralization, then it increases because the cations it contains are replaced by H+ ions. The pH of CPL1 obtained is around 1, and the conductivity of CPL1 is approximately 12 mS / cm.The conductivity of the acid solution, i.e. HCl, at the outlet of the first compartment 220 is reduced by approximately 74%, and the conductivity of the brine, i.e. NaCl, obtained at the outlet of the third compartment 230, is increased by approximately 234%. The reduction in cations is approximately 84%.

[0218] 2- Cationic substitution on the electrodialyzer 5 ([Fig.1]) The electrodialyzer 5 comprises, for example, 5 to 15 cells 15. The first compartment 20 is supplied with an HCl solution having a conductivity greater than or equal to 100 mS / cm, in particular greater than or equal to 150 mS / cm. The second compartment 26 is supplied with CPL as exemplified above. The third compartment is initially supplied with a NaCl solution having a conductivity less than or equal to 50 mS / cm, in particular less than or equal to 25 mS / cm, in this specific example, less than or equal to 15 mS / cm. A current (I) greater than or equal to 1 ampere, in particular less than or equal to 2 amperes, is applied to the electrodialyzer 5, and the voltage is preferably left free. At the beginning of electrodialysis ii), the conductivity of CPL decreases, indicating its demineralization, then it increases because the cations it contains are replaced by H+ ions.In the acid compartment 20, conductivity decreases due to the depletion of H+ ions and the production of NaCl, which is less conductive. The cations extracted from CPL migrate into the brine compartment 30, which becomes enriched in multivalent cations that are more conductive than NaCl. The pH of CPL1 obtained is around 1, and the conductivity of CPL1 is approximately 12 mS / cm. The conductivity of the acid solution exiting the first compartment 220 is reduced by approximately 35%, and the conductivity of the brine obtained exiting the third compartment 30 is increased by approximately 25%. The cation reduction is approximately 82%.

[0219] For the implementation of step iii), the CPL1 used may be either that which of the 5 or 200 electrodialyzer since the latter have identical performance in terms of cation removal rate.

[0220] For the purposes of the tests described below, a milk protein composition, CPL”, was prepared by dispersing a 17% dry mass sweet whey powder (raw) in demineralized water. The dispersion was mechanically stirred until a homogeneous mixture was obtained. CPL” thus has the following parameters: dry matter mass percentage: 17% (powder mass / total mass); pH = 5; initial conductivity: 12 mS / cm; ash mass percentage: 8%; lactose mass percentage: 74%; cation mass percentage (including Na, NH4, K, Ca, Mg): 5%; anion mass percentage (including Cl, NO3, PO4, SO4): 3%; The different mass ratios (with the exception of that in dry matter) are calculated by relating the total mass of one or more compound(s) to the total mass of the dry matter.

[0221] 3. Cationic substitution on the electrodialyzer 200 (ESC) ([Fig.3])

[0222] The electrodialyzer 200 comprises, for example, 5 to 15 cells 215. The first compartment 220 is supplied with an HCl solution having a conductivity greater than or equal to 100 mS / cm, in particular greater than or equal to 150 mS / cm. The second compartment 226 is supplied by CPL' ' exemplified above. The third compartment is supplied with a NaCl solution having a conductivity less than or equal to 50 mS / cm, in particular less than or equal to 25 mS / cm, in this specific example, less than or equal to 15 mS / cm. A current (I) greater than or equal to 2 amperes, in particular less than or equal to 3 amperes, is applied to the electrodialyzer 200, and the voltage is preferably left free. During electrodialysis ii), the conductivity of CPL' decreases, indicating its demineralization, then it increases because the cations it contains are replaced by H+ ions. The pH of CPL1' obtained is around 2, and the conductivity of CPL1' is approximately 12 mS / cm.The conductivity of the acid solution, i.e., HCl, at the outlet of the first compartment 220 is reduced by approximately 53%, and the conductivity of the brine, i.e., NaCl, obtained at the outlet of the third compartment 230, is increased by approximately 292%. The cation reduction (or substitution rate) is approximately 77%. The anion rate, on the other hand, is essentially similar between CPL1 and CPL2.

[0223] 4. Conventional two-compartment electrodialysis (ED) (Anionic Membrane / Cationic Membrane) (for example step (iii) 10 or 205 of [Fig.l] or 3)

[0224] This electrodialyzer comprises, for example, 5 to 15 cells. The first compartment is supplied by CPL1 as described above, and the second compartment is initially supplied with a salt, in particular sodium chloride, having a conductivity greater than or equal to 5 mS / cm and less than or equal to 15 mS / cm. During the test, a voltage greater than or equal to 10V and less than or equal to 20V, in particular less than or equal to 15V, is applied to the two-compartment electrodialyzer, and the current (I) is left free. During the test, the conductivity of CPL1” decreases, indicating its demineralization. Some of the H+ ions are extracted into the brine compartment, hence the increase in the pH of CPL1”(ESC + ED) at the outlet, particularly to a pH greater than or equal to 2.5, and notably greater than or equal to 3. The final conductivity of CPL1”(ESC + ED) is reduced by approximately 90% compared to CPL, thanks to this conventional electrodialysis. The cation removal rate (Na, NH4, K, Ca, Mg) in CPL1”(ESC + ED) is greater than or equal to 90% (compared to CPL1” obtained at the outlet of the cationic substitution ED, [Fig. 3]). The anion removal rate (Cl, NO3, PO4, SO4) in CPL1”(ESC + ED) is greater than or equal to approximately 80% (compared to CPL1” obtained at the output of the cationic substitution ED, [Fig.3]).

[0225] It is possible to add a basic solution (for example a 5% w / w sodium hydroxide solution) to the recovered CPL2 to adjust its pH to the desired pH.

[0226] It is also possible to add said basic solution to the compartments of the electrodialyzer in step (ii) receiving CPL1 concurrently with the extraction of cations and anions, and therefore under the application of the electric field. This route makes it possible to raise the pH while demineralizing CPL1. Furthermore, a synergistic effect has been observed because the extraction of phosphate ions, and of calcium and magnesium ions, is improved compared to demineralization using ED without the addition of a base.

[0227] For the testing described below, a milk protein composition, CPL(A), was supplied at 23% dry matter. The milk protein composition is a sweet whey pre-concentrated by evaporation. CPL(A) thus has the following parameters: dry matter mass percentage: 23% (dry matter / total mass); pH = 6.04; initial conductivity: 12.2 mS / cm; ash mass percentage: 7.6% (% ash mass / total dry matter); crude protein mass percentage: 15.7% (% crude protein mass / total dry matter); 541 mg Na / 100g total dry matter; 2269 mg K / 100g total dry matter; 513 mg Ca / 100g total dry matter; 104 mg Mg / 100g total dry matter; 1357 mg of Cl / 100g of total dry matter; 640 mg of Phosphorus / 100g of total dry matter.

[0228] 5. Cationic substitution on the electrodialyzer 200 (ESC) ([Fig.3])

[0229] The electrodialyzer 200 comprises, for example, 5 to 25 cells 215. The first compartment 220 is supplied with an HCl solution having a conductivity greater than or equal to 100 mS / cm, in particular greater than or equal to 150 mS / cm. The second compartment 226 is supplied with CPL(A) as exemplified above. The third compartment is supplied with water. A current (I) greater than or equal to 2 amperes, in particular less than or equal to 10 amperes, is applied to the electrodialyzer. 200, and the voltage is preferably left free. During electrodialysis ii), the conductivity of CPL(A) decreases, indicating its demineralization, then it increases because the cations it contains are replaced by H+ ions. The pH of CPL1(A) obtained is around 2, and the conductivity of CPL1(A) is approximately 8.0 mS / cm. The conductivity of the acidic solution, i.e., HCl, at the outlet of the first compartment 220 is lowered, and at the outlet of the third compartment 230, the water has become ionized and contains brine. The following profile is obtained for the cations of CPL1(A): 166 mg of Na / 100g of total dry matter; 378 mg of K / 100g of dry matter; 314 mg of Ca / 100g of total dry matter; 79 mg of Mg / 100g of total dry matter. The anion content is, however, substantially similar between CPL(A) and CPL1 (A).

[0230] 6. Conventional two-compartment electrodialysis (ED) (Anionic Membrane / Cationic Membrane) (e.g., electrodialyzer 10 or 205 of [Fig. 1] or 3)

[0231] This electrodialyzer comprises, for example, 5 to 50 cells. The first compartment is supplied with CPL1(A) described above, and the second compartment is supplied with water. During the test, a voltage greater than or equal to 10 V and less than or equal to 50 V, in particular less than or equal to 40 V, is applied to the two-compartment electrodialyzer, and the current (I) is left free. During the test, the conductivity of CPL1(A) decreases, indicating its demineralization. Some of the H+ ions are extracted into the brine compartment, hence the increase in the pH of CPL1(A) at the outlet.

[0232] In one embodiment, the addition of a 5% (w / w) basic solution is carried out on CPL2 after step (iii) and not during step (iii).

[0233] In this case, the pH of CPL2 obtained at the outlet of step (iii) (before the addition of sodium hydroxide) is approximately 4.5. CPL2 at the outlet of step (iii) has a conductivity of approximately 0.3 mS / cm. The following ionic profile is obtained: approximately 0 mg of Na₂ / 100 g of total dry matter; approximately 0 mg of K₂ / 100 g of total dry matter; 35 mg of Ca₂ / 100 g of total dry matter; 19 mg of Mg₂ / 100 g of total dry matter; 14 mg of Cl₂ / 100 g of total dry matter; 206 mg of phosphorus / 100 g of total dry matter. The cation removal rate is 98%, and the anion removal rate is 89%.

[0234] In another embodiment, the addition of the basic solution is carried out on CPL1 during step (iii) simultaneously with the extraction of anions and cations, under the application of an electric field. A 5% (w / w) sodium hydroxide (NaOH) solution is added to the electrodialyzer compartments in step (iii) including CPL1. Preferably, this addition is carried out after a reduction of approximately 75% of the conductivity observed on the ED (iii). Preferably, the addition of sodium hydroxide is carried out when CPL1 has a conductivity less than or equal to 1 mS / cm, in this specific example of the order of 0.5 mS / cm, and / or at a pH greater than or equal to 3, in particular greater than or equal to 4.

[0235] In this case, the pH of CPL2 obtained at the outlet of step (iii) is approximately 5.2. CPL2 at the outlet of step (iii) has a conductivity of approximately 0.3 mS / cm. The following ionic profile is obtained: approximately 53 mg of Na / 100 g of total dry matter; approximately 0 mg of K / 100 g of total dry matter; 24 mg of Ca / 100 g of total dry matter; 13 mg of Mg / 100 g of total dry matter; 9 mg of Cl / 100 g of total dry matter; 160 mg of phosphorus / 100 g of total dry matter. The ash content is 0.50% (% ash mass / total dry matter). The cation removal rate is 97%, and the anion removal rate is 92%.

[0236] The addition of a basic solution during ED (iii) under the application of an electric field improves the extraction of phosphate ions and divalent cations compared to ED (iii) without the addition of the basic solution.

[0237] In a comparative embodiment, step (ii) does not include the addition of a basic solution, and the demineralization process includes an exclusively anionic substitution step on an electrodialyzer whose cells comprise three CPL2(A) compartments, as described herein, carried out after step (ii). In this case, the pH of the resulting milk protein composition is approximately 5.4, for a conductivity of approximately 0.2 mS / cm. The following ionic profile is obtained: approximately 19 mg of Na₂ / 100 g of total dry matter; approximately 2 mg of K₂ / 100 g of total dry matter; 39 mg of Ca₂ / 100 g of total dry matter; 37 mg of Mg₂ / 100 g of total dry matter; 11 mg of Cl₂ / 100 g of total dry matter; 110 mg of phosphate / 100 g of total dry matter. The ash content is 0.40% (% ash mass / total dry mass).The mass fractions of divalent cations are higher than those obtained above compared to step (iii) during a period in which a basic solution is added.

[0238] Step (iii) with the addition of a base during the latter under an electric field, combined with step (ii), improves the extraction of divalent cations by about 30% and the extraction of phosphates by about 20% compared to step (iii) without the addition of sodium hydroxide during the latter and combined with step (ii), and the extraction of divalent cations by about 44% compared to the comparative embodiment.

[0239] Step (iii) described in point 6 can also be applied to CPL1 obtained in point 1 or in point 2 for obtaining CPL2.

Claims

Claims

1. Method for manufacturing a demineralized dairy protein composition (CPL2), characterized in that it comprises the following steps: (i)- providing a dairy protein composition (CPL); (ii)- electrodialysis of the dairy protein composition (CPL) on an electrodialyzer (5,200), comprising cellular units (15, 215) comprising three compartments (20,26,30; 220,226,230), and configured to substitute at least one cation with at least one hydrogen ion H+ in the dairy protein composition (CPL) to obtain an at least partially demineralized and acidified dairy protein composition (CPL1); (iü)- electrodialysis of the dairy protein composition (CPL1) obtained in step (ii); (iv)- recovery of the demineralized milk protein composition (CPL2) and in that said method comprises the addition of at least one basic solution to the milk protein composition during step (iü) and / or after step (iii).

2. Manufacturing method according to claim 1, characterized in that said at least one basic solution is a solution comprising at least one basic salt.

3. Manufacturing method according to claim 2, characterized in that the addition of the basic solution is carried out during at least part of the electrodialysis step (iii) concomitantly with the extraction of the ions.

4. Manufacturing method according to either of claims 2 and 3, characterized in that the addition of the basic solution to the milk protein composition is carried out when the milk protein composition has a conductivity less than or equal to 1 mS / cm, and preferably has a pH greater than or equal to 3.

5. Manufacturing process according to any one of claims 2 to 4, characterized in that after the addition of the basic solution, the milk protein composition has a pH greater than or equal to 4.5, preferably greater than or equal to 5.

0.

6. Manufacturing method according to any one of claims 1 to 5, characterized in that the electrodialysis step (iii) comprises the extraction of anions and cations.

7. Manufacturing method according to any one of claims 1 to 6, characterized in that step (ii) is an exclusive substitution step- sively of cations.

8. Manufacturing process according to any one of claims 1 to 7, characterized in that the milk protein composition recovered in step (iv) (CPL2) comprises phosphate ions (H2PO4, HPO42, PO4 3 ) whose phosphorus mass is greater than or equal to 110 mg, preferably greater than or equal to 150 mg, per 100 g of total dry mass of said recovered milk protein composition (CPL2).

9. Manufacturing process according to any one of claims 1 to 8, characterized in that the milk protein composition recovered in step (iv) (CPL2) comprises sodium or potassium ions, the mass of which is greater than or equal to 20 mg, preferably greater than or equal to 30 mg, per 100g of total dry mass of said recovered milk protein composition (CPL2).

10. Manufacturing method according to any one of claims 1 to 9, characterized in that the compartments of the electrodialyzer of step (ii) receiving the milk protein composition (MPC) are each delimited between two cationic membranes (24, 28; 224, 228).

11. Manufacturing method according to any one of claims 1 to 10, characterized in that it comprises a treatment step (v) of at least a portion of the salt(s) chosen from the following salts: - the salt(s) originating directly from the electrodialysis step ii), - the salt(s) originating indirectly from the electrodialysis step ii), - the salt(s) originating directly from the electrodialysis step iii), - the salt(s) originating indirectly from the electrodialysis step iii), - the salt(s) originating from a preliminary demineralization step carried out on the dairy protein composition upstream of step i), - a mixture of the latter, said treatment step (v) being configured to produce one or more acid salt(s) on the one hand, and / or one or more basic salt(s) on the other hand.

12. Manufacturing method according to claim 11, characterized in that the treatment step (v) consists of an electrodialysis step carried out on an electrodialyzer with bipolar membrane(s) (70).

13. Manufacturing method according to claim 12, characterized in that the electrodialyzer with bipolar membrane(s) (70), in step (v), comprises cellular units (105) comprising three compartments A, B and C (110,116,120), compartments A and B are supplied with water and compartment C is supplied with said salt(s), in particular compartment C arranged between compartments A and B.

14. Manufacturing method according to claim 13, characterized in that at least a portion of the salt(s), in particular hydrochloric acid and / or sulfuric acid, obtained during treatment step (v), is / are supplied to one of the three compartments (20, 26, 30; 220, 226, 230) of the electrodialyzer (5, 200) in step ii).

15. Manufacturing process according to any one of claims 11 to 14, characterized in that the basic solution comprises at least in part one or more basic salt(s), in particular sodium hydroxide and / or potassium hydroxide, obtained during treatment step (v).

16. Manufacturing process according to any one of claims 1 to 15, characterized in that the basic solution comes at least in part from the recycling of an effluent from step ii) and / or step iii).

17. Manufacturing process according to any one of claims 1 to 16, characterized in that the milk protein composition is chosen from the list comprising: a whey, such as a sweet whey or an acid whey or a mixture thereof; a milk ultrafiltration permeate; a milk microfiltration permeate; a whey ultrafiltration retentate or permeate; a milk microfiltration permeate ultrafiltration retentate or permeate; or a mixture thereof, preferably a whey.

18. Installation for implementing the method according to any one of claims 1 to 17, characterized in that it comprises: a) a first electrodialyser (5, 200) comprising a first inlet intended to receive a dairy protein composition (CPL), said electrodialyser comprising cellular units (15, 215) comprising three compartments (20, 26, 30; 220, 226, 230), and configured to substitute at least one cation with at least one hydrogen ion H+ in the dairy protein composition (CPL), and a first outlet for an at least partially demineralized and acidified dairy protein composition (CPL1);b) a second electrodialyzer (10,205) comprising a first inlet intended to receive the milk protein composition (CPL1) obtained in step (ii), and a first outlet for the milk protein composition (CPL2), and in that said installation comprises: c) a device comprising a basic solution and configured to be in fluid communication for a given time with the compartments of the second electrodialyzer intended to receive the composition; milk protein (CPL1), preferably under the application of an electric field.

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