US20090214740A1 - Method for the preparation of a stable alkali metal lactate in powder form - Google Patents

Method for the preparation of a stable alkali metal lactate in powder form Download PDF

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Publication number
US20090214740A1
US20090214740A1 US12/359,806 US35980609A US2009214740A1 US 20090214740 A1 US20090214740 A1 US 20090214740A1 US 35980609 A US35980609 A US 35980609A US 2009214740 A1 US2009214740 A1 US 2009214740A1
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alkali metal
powder
metal lactate
lactate
preparation
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US12/359,806
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Eloy E. Urbano CRUZ
Peter Paul Jansen
Bert Theo De Vegt
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Purac Biochem BV
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Purac Biochem BV
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/01—Saturated compounds having only one carboxyl group and containing hydroxy or O-metal groups
    • C07C59/08—Lactic acid
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41—Preparation of salts of carboxylic acids
    • C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part

Definitions

  • the invention relates to the preparation of a stable alkali metal lactate in powder form, in particular, a stable sodium lactate in powder form, the product of said preparation, functional pre-mixes for foodstuff comprising said stable alkali metal lactate powder, and foodstuffs comprising said stable alkali metal lactate powder.
  • Sodium lactate is, inter alia, an important constituent in various flavouring mixtures.
  • a flavouring mixture in powder form it is important to be able to use sodium lactate in powder form.
  • the stability of, in particular, open packs is an important criterion here.
  • the stability of the sodium lactate in powder form is preferably at least 48 hours.
  • Sodium lactate in powder form is currently produced by crystallisation of a concentrated sodium lactate solution in absolute ethanol. Because of its highly hygroscopic properties, this powder has limited stability; it absorbs moisture very rapidly and in doing so forms a viscous fluid (as a rule within one hour and often after only 15 minutes).
  • Netherlands Patent Application 7106959 discloses a method for the preparation of sodium lactate in powder form with which an aqueous sodium lactate solution is spray-dried in a spray tower. With this method a glassy product may be formed on the wall of the spray tower.
  • the starting point for the present invention is a different method for removing water wherein sodium lactate is made in powder form in a less-energy costly way. The powder obtained with said method appears to have the desired stability.
  • the invention provides a solution to the stability problem described above and relates to a method for the preparation of a stable alkali metal lactate in powder form, wherein a concentrate that contains alkali metal lactate is processed, with cooling, in a mixer/extruder to form a powder of the alkali metal lactate.
  • the alkali metal lactate is preferably lithium lactate, sodium lactate or potassium lactate and, in particular, sodium lactate. According to the invention the alkali metal lactates in powder form are stable for at least 48 hours.
  • the starting material used for the preparation of the concentrate is an aqueous solution of the alkali metal lactate. This 50-70% (m/m), preferably 55-65% (m/m), aqueous solution is preferably first treated with active charcoal before the solution is concentrated to 60-100% (m/m), preferably 80-100% (m/m), most preferably 90-100% (m/m).
  • the processing in an extruder/mixer is preferably carried out at a starting temperature of 110° C. to 170° C., preferably 130° C. to 165° C.
  • the cooling ranges from 10° C. to 100° C., preferably 20° C. to 90° C.
  • Suitable extrude/mixers are Haake Rheomix 600 Models®, Hobart mixers, Werner & Pfliederer Models®, APV-Baker mixer/extruders, Simon Freres MXT models or any other comparable extruder/mixers known in the art.
  • the concentrate can first be cooled in a heat extractor column as a pretreatment.
  • the concentrate is cooled, under the influence of gravity, in counter-current with air/nitrogen in the boat extractor column, the concentrate being cooled by 20°-50° C. with respect to the starting temperature.
  • the alkali metal lactate may be combined with a carrier. Said combining with a carrier may be conducted prior to being processed with cooling in the mixer/extruder to directly form a powder comprising the alkali metal lactate.
  • the concentrate used, as a starting material may be relatively low concentrated: down to 60% (m/m).
  • the alkali metal lactate may also be combined with a carrier after processing the concentrate with an extruder/mixer, with cooling.
  • the carrier that is used herein is preferably a flour, a starch, a silicate or an alkaline earth metal lactate.
  • the flour is preferably rice flour.
  • the starch is preferably cornstarch, wheat starch or pea starch.
  • the silicates are preferably food-grade silicas such as Sipernat® 22S and 50S, ex Degussa and Zeothix 265.
  • the alkaline earth metal lactate is preferably calcium lactate. With this method the ratio of alkali metal lactate carrier varies from 50:50 to 10:90, and preferably 50:50 to 40:60, based on the weight of the alkali metal lactate comprising powder.
  • this embodiment encompasses a method for the preparation of a stable alkali metal lactate in powder form, comprising the steps of:
  • step (b) mixing the powder from step (a) with a carrier to form a powder containing alkali metal lactate.
  • the ratio of alkali metal lactate powder:carrier is at least 99:1 to 50:50 and preferably 80:20 based on the weight of the alkali metal lactate comprising powder.
  • the alkali metal lactate powder is preferably ground, preferably in a conical flourmill or a hammer mill, to the desired particle size before step (b).
  • This particle size is preferably less than 800 ⁇ m and in particular is 200 to 800 ⁇ m.
  • Step (b) of the method according to the above-described embodiment is preferably carried out in a mixer, for example, a Hobart mixer, a Turbula Nauta or Forberg mixer, at ambient temperature.
  • a mixer for example, a Hobart mixer, a Turbula Nauta or Forberg mixer, at ambient temperature.
  • the stability of the stable alkali metal lactate in powder form can be even further increased by adding a suitable emulsifier, for example, sodium stearyl lactate or lecithin, either during the processing in the extruder/mixture or in step (b) when conducted.
  • a suitable emulsifier for example, sodium stearyl lactate or lecithin
  • the stability and the product characteristics of the stable alkali metal lactate in powder form can be adjusted with the aid of these additives, the requisite stability duration of at least 48 hours always being met.
  • the alkali metal lactate powder obtained with the methods according to the invention have a stability of at least 48 hours which renders it novel and are therefore, also subject of this invention. Owing to its stability the alkali metal lactate powder according to the invention appears highly suitable for use in foodstuffs arid even for functional pre-mixes for foodstuffs. Additional ingredients for functional pre-mixes comprise spices, preservatives, colourings and flavourings, etc. Said pre-mixes may be prepared by either combining the stable alkali metal lactate containing powder with the other ingredients or the other ingredients may be added to the alkali metal lactate at any stage during preparation of the stable alkali metal lactate containing powder.
  • the alkali metal lactate powder according to the invention before being used in various applications, is preferably ground to a particle size of less than 800 ⁇ m, more preferably to a particle size between 200-800 ⁇ m.
  • the invention is also directed to foodstuffs and functional pre-mixes comprising the stable alkali metal lactate powder according to the invention.
  • aqueous solution of sodium lactate that contained 60-65% (m/m) sodium lactate was evaporated, either under atmospheric pressure or under reduced pressure, to give a concentrate that contained 90% (m/m) sodium lactate.
  • the aqueous solutions that contained 60-65% (m/m) sodium lactate were combined with a carrier.
  • the carriers used were potato starch, wheat starch, corn starch, tapioca and additives such as Capsul E, sunflower oil, Esterlac EFF, salt, lecithin, glycerol, Tween 80, Span 80, and glycerol.
  • the concentrate and the carrier were processed in a Haake Rheomix 600 model mixer/extruder to give a powder comprising about 42% (m/m) sodium lactate.
  • the mixing times and processing temperatures were, respectively, 5 to 30 minutes and 90° C. to 130° C.
  • the powder consisted of individual rubbery grains. These grains were stable for at least 48 hours (of the order of 2 to 5 days).
  • the stability of the powder was tested as follows: 5-gram sample and a 100-grain sample, respectively, of each powder were placed in an aluminum cup and in a plastic bag (26 ⁇ 34 cm). The stability tests were carried out in a climate-controlled chamber at 30, 60 and 70% relative humidity and at a temperature of 20° C. The values for the water absorption by the powder samples (that is to say the stability) were determined when the powder samples had visibly clearly absorbed water.
  • An aqueous solution of sodium lactate that contained 60-65 % (m/m) sodium lactate was evaporated, either under atmospheric pressure or under reduced pressure, to give a concentrate that contained 93-100% (m/m) sodium lactate.
  • the concentrate was fed at a temperature of 150°-160° C. to an APV-Baker mixer/extruder.
  • a heat extractor column was used as pretreatment for the stream that was fed to the mixer/extruder.
  • the concentrate introduced was cooled under the influence of gravity in counter-current with air/nitrogen; during this operation the concentrate was cooled by 20°-50° C.
  • the product was cooled in a mixer/extruder to a final temperature of 20°-60° C.; the residence time in the mixer/extruder was 2 to 9 minutes.
  • the product was then ground in a conical flourmill, the particle size of the ground product being less than 600 ⁇ m.
  • the ground product was mixed with a carrier in a Hobart mixer for 10 to 120 minutes in an air or a nitrogen atmosphere.
  • the carriers used were rice flour, cornstarch, pea starch, wheat starch, the silicate Sipemat 22S or the silicate Zeothix 265.
  • the sodium lactate:carrier ratio was 60:40, based on the pulverulent sodium lactate.

Abstract

The invention relates to a method for the preparation of a stable alkali metal lactate in powder form, the product of said preparation, functional pre-mixes for foodstuff comprising said stable alkali metal lactate powder, and foodstuffs comprising said stable alkali metal lactate powder. In the method According to the invention, a concentrate that contains alkali metal lactate is processed, with cooling, in a mixer/extruder to form a powder of the alkali metal lactate. According to the invention the alkali metal lactates in powder form are stable for at least 48 hours.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a Divisional Application of U.S. patent application Ser. No. 10/265,633, filed Oct. 8, 2002, the entire contents of which is incorporated herein by reference for any and all purposes.
    • FIELD OF THE INVENTION
  • The invention relates to the preparation of a stable alkali metal lactate in powder form, in particular, a stable sodium lactate in powder form, the product of said preparation, functional pre-mixes for foodstuff comprising said stable alkali metal lactate powder, and foodstuffs comprising said stable alkali metal lactate powder.
    • BACKGROUND OF THE INVENTION
  • Sodium lactate is, inter alia, an important constituent in various flavouring mixtures. For the preparation of a flavouring mixture in powder form, it is important to be able to use sodium lactate in powder form. The stability of, in particular, open packs is an important criterion here. For good processing of sodium lactate in powder form in such flavouring mixtures, the stability of the sodium lactate in powder form is preferably at least 48 hours.
  • Sodium lactate in powder form is currently produced by crystallisation of a concentrated sodium lactate solution in absolute ethanol. Because of its highly hygroscopic properties, this powder has limited stability; it absorbs moisture very rapidly and in doing so forms a viscous fluid (as a rule within one hour and often after only 15 minutes).
  • Netherlands Patent Application 7106959 discloses a method for the preparation of sodium lactate in powder form with which an aqueous sodium lactate solution is spray-dried in a spray tower. With this method a glassy product may be formed on the wall of the spray tower.
  • This can largely be prevented by spray-drying a cooking salt solution first and then spray-drying the sodium lactate solution. This product, however, lacks the desired stability. The starting point for the present invention is a different method for removing water wherein sodium lactate is made in powder form in a less-energy costly way. The powder obtained with said method appears to have the desired stability.
    • SUMMARY OF THE INVENTION
  • The invention provides a solution to the stability problem described above and relates to a method for the preparation of a stable alkali metal lactate in powder form, wherein a concentrate that contains alkali metal lactate is processed, with cooling, in a mixer/extruder to form a powder of the alkali metal lactate.
    • DESCRIPTION OF THE SPECIFIC EMBODIMENTS
  • According to the invention, the alkali metal lactate is preferably lithium lactate, sodium lactate or potassium lactate and, in particular, sodium lactate. According to the invention the alkali metal lactates in powder form are stable for at least 48 hours.
  • The starting material used for the preparation of the concentrate is an aqueous solution of the alkali metal lactate. This 50-70% (m/m), preferably 55-65% (m/m), aqueous solution is preferably first treated with active charcoal before the solution is concentrated to 60-100% (m/m), preferably 80-100% (m/m), most preferably 90-100% (m/m).
  • According to the invention, the processing in an extruder/mixer is preferably carried out at a starting temperature of 110° C. to 170° C., preferably 130° C. to 165° C. The cooling ranges from 10° C. to 100° C., preferably 20° C. to 90° C. Suitable extrude/mixers are Haake Rheomix 600 Models®, Hobart mixers, Werner & Pfliederer Models®, APV-Baker mixer/extruders, Simon Freres MXT models or any other comparable extruder/mixers known in the art.
  • If it is desirable or necessary to shorten the length of the mixer/extruder, the concentrate can first be cooled in a heat extractor column as a pretreatment. In this case, the concentrate is cooled, under the influence of gravity, in counter-current with air/nitrogen in the boat extractor column, the concentrate being cooled by 20°-50° C. with respect to the starting temperature.
  • In order to improve the stability of the alkali metal lactate powder even more, the alkali metal lactate may be combined with a carrier. Said combining with a carrier may be conducted prior to being processed with cooling in the mixer/extruder to directly form a powder comprising the alkali metal lactate. With this method the concentrate used, as a starting material, may be relatively low concentrated: down to 60% (m/m). The alkali metal lactate may also be combined with a carrier after processing the concentrate with an extruder/mixer, with cooling.
  • The carrier that is used herein is preferably a flour, a starch, a silicate or an alkaline earth metal lactate. The flour is preferably rice flour. The starch is preferably cornstarch, wheat starch or pea starch. The silicates are preferably food-grade silicas such as Sipernat® 22S and 50S, ex Degussa and Zeothix 265. The alkaline earth metal lactate is preferably calcium lactate. With this method the ratio of alkali metal lactate carrier varies from 50:50 to 10:90, and preferably 50:50 to 40:60, based on the weight of the alkali metal lactate comprising powder.
  • As mentioned above, the carrier can also be combined with the alkali metal lactate after extrusion. Thus, this embodiment encompasses a method for the preparation of a stable alkali metal lactate in powder form, comprising the steps of:
  • (a) processing a concentrate that contains an alkali metal lactate, with cooling, in a mixer/extruder to give a powder of the alkali metal lactate; and
  • (b) mixing the powder from step (a) with a carrier to form a powder containing alkali metal lactate.
  • It was found that with this method a higher concentration of alkali metal lactate in the powder may be obtained compared with the powder obtained with combined extrusion. With this method the ratio of alkali metal lactate powder:carrier is at least 99:1 to 50:50 and preferably 80:20 based on the weight of the alkali metal lactate comprising powder.
  • The alkali metal lactate powder is preferably ground, preferably in a conical flourmill or a hammer mill, to the desired particle size before step (b). This particle size is preferably less than 800 μm and in particular is 200 to 800 μm.
  • Step (b) of the method according to the above-described embodiment is preferably carried out in a mixer, for example, a Hobart mixer, a Turbula Nauta or Forberg mixer, at ambient temperature.
  • The stability of the stable alkali metal lactate in powder form can be even further increased by adding a suitable emulsifier, for example, sodium stearyl lactate or lecithin, either during the processing in the extruder/mixture or in step (b) when conducted. The stability and the product characteristics of the stable alkali metal lactate in powder form can be adjusted with the aid of these additives, the requisite stability duration of at least 48 hours always being met.
  • The alkali metal lactate powder obtained with the methods according to the invention have a stability of at least 48 hours which renders it novel and are therefore, also subject of this invention. Owing to its stability the alkali metal lactate powder according to the invention appears highly suitable for use in foodstuffs arid even for functional pre-mixes for foodstuffs. Additional ingredients for functional pre-mixes comprise spices, preservatives, colourings and flavourings, etc. Said pre-mixes may be prepared by either combining the stable alkali metal lactate containing powder with the other ingredients or the other ingredients may be added to the alkali metal lactate at any stage during preparation of the stable alkali metal lactate containing powder. Irrespective of the preparation method used, the alkali metal lactate powder according to the invention, before being used in various applications, is preferably ground to a particle size of less than 800 μm, more preferably to a particle size between 200-800 μm. The invention is also directed to foodstuffs and functional pre-mixes comprising the stable alkali metal lactate powder according to the invention.
  • The invention is further elucidated by the examples, which are to be construed as illustrative only and not as being limitative.
    • EXAMPLES Example 1
  • An aqueous solution of sodium lactate that contained 60-65% (m/m) sodium lactate was evaporated, either under atmospheric pressure or under reduced pressure, to give a concentrate that contained 90% (m/m) sodium lactate. In additional experiments the aqueous solutions that contained 60-65% (m/m) sodium lactate were combined with a carrier. The carriers used were potato starch, wheat starch, corn starch, tapioca and additives such as Capsul E, sunflower oil, Esterlac EFF, salt, lecithin, glycerol, Tween 80, Span 80, and glycerol. The concentrate and the carrier were processed in a Haake Rheomix 600 model mixer/extruder to give a powder comprising about 42% (m/m) sodium lactate. The mixing times and processing temperatures were, respectively, 5 to 30 minutes and 90° C. to 130° C. The powder consisted of individual rubbery grains. These grains were stable for at least 48 hours (of the order of 2 to 5 days).
  • The stability of the powder was tested as follows: 5-gram sample and a 100-grain sample, respectively, of each powder were placed in an aluminum cup and in a plastic bag (26×34 cm). The stability tests were carried out in a climate-controlled chamber at 30, 60 and 70% relative humidity and at a temperature of 20° C. The values for the water absorption by the powder samples (that is to say the stability) were determined when the powder samples had visibly clearly absorbed water.
    • Example 2
  • An aqueous solution of sodium lactate that contained 60-65 % (m/m) sodium lactate was evaporated, either under atmospheric pressure or under reduced pressure, to give a concentrate that contained 93-100% (m/m) sodium lactate. The concentrate was fed at a temperature of 150°-160° C. to an APV-Baker mixer/extruder. In order to reduce the length of the extruder, in a number of experiments a heat extractor column was used as pretreatment for the stream that was fed to the mixer/extruder. In the heat extractor column the concentrate introduced was cooled under the influence of gravity in counter-current with air/nitrogen; during this operation the concentrate was cooled by 20°-50° C. Irrespective of whether or not a heat extractor column was used, the product was cooled in a mixer/extruder to a final temperature of 20°-60° C.; the residence time in the mixer/extruder was 2 to 9 minutes. The product was then ground in a conical flourmill, the particle size of the ground product being less than 600 μm. The ground product was mixed with a carrier in a Hobart mixer for 10 to 120 minutes in an air or a nitrogen atmosphere. The carriers used were rice flour, cornstarch, pea starch, wheat starch, the silicate Sipemat 22S or the silicate Zeothix 265. The sodium lactate:carrier ratio was 60:40, based on the pulverulent sodium lactate.
  • For the stability tests a 5-gram sample and a 100-gram sample, respectively, of each powder was placed in a plastic dish (4×3 cm) and in a plastic bag (26×34 cm), respectively. The stability tests were carried out in a climate-controlled chamber at a relative humidity of 60% and a temperature of 20° C. For the 100 g sample the values for the moisture absorption by the samples were determined when the sample had visibly clearly absorbed water. The end products were found to be stable to moisture absorption for a period of 48 to 72 hours.

Claims (11)

1. A method for the preparation of a stable alkali metal lactate in powder form, comprising processing at a starting temperature of 130° C. to 170° C. an aqueous concentrate of 60-100% (m/m) alkali metal lactate cooling the alkali metal lactate to form a powder of the alkali metal lactate, wherein (i) the processing and cooling is performed in a mixer/extruder (ii) and the alkali metal lactate is combine with a carrier before or after processing.
2. A stable alkali metal lactate powder obtainable by the method of claim 1 wherein the alkali metal lactate powder has a stability of at least 48 hours.
3. A functional pre-mix comprising a stable alkali metal lactate powder according to claim 1.
4. A functional pre-mix comprising a stable alkali metal lactate powder according to claim 2.
5. A method for the preparation or preservation of foodstuff comprising adding a stable alkali metal lactate according to claim 1 to a foodstuff.
6. A method for the preparation or preservation of foodstuff comprising adding a stable alkali metal lactate according to claim 2 to a foodstuff.
7. A method for the preparation or preservation of foodstuff comprising adding a functional pre-mix according to claim 3 to a foodstuff.
8. A method for the preparation or preservation of foodstuff comprising adding a functional premix according to claim 4 to a foodstuff.
9. A foodstuff comprising a stable alkali metal lactate powder according to claim 1.
10. A foodstuff comprising a stable alkali metal lactate powder according to claim 2.
11. A foodstuff comprising a functional pre-mix according to claim 4.
US12/359,806 2001-10-08 2009-01-26 Method for the preparation of a stable alkali metal lactate in powder form Abandoned US20090214740A1 (en)

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US10/265,633 US7494684B2 (en) 2001-10-08 2002-10-08 Method for the preparation of a stable alkali metal lactate in powder form
US12/359,806 US20090214740A1 (en) 2001-10-08 2009-01-26 Method for the preparation of a stable alkali metal lactate in powder form

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EP (2) EP1434753B1 (en)
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AT (1) ATE538082T1 (en)
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019068798A1 (en) 2017-10-05 2019-04-11 Purac Biochem B.V. Lactate powder and method for the preparation thereof
CN110642702A (en) * 2019-09-10 2020-01-03 湖北壮美生物科技有限公司 Industrial preparation device of sodium lactate powder with high purity and low water content and corresponding preparation method

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020187231A1 (en) * 2001-05-09 2002-12-12 Symone Kok Process for the removal of undesired flavour and odour components from potassium lactate
ES2378658T3 (en) * 2001-10-08 2012-04-16 Purac Biochem B.V. Method for the preparation of a stable alkali metal lactate in powder form
EP1616851A1 (en) * 2004-07-15 2006-01-18 PURAC Biochem BV Method for the preparation of a stable lactate metal salt in powder form and stable metal lactate salt
US20080138425A1 (en) * 2004-07-15 2008-06-12 Kees Bert Geerse Method for the Preparation of a Stable Lactate Metal Salt in Powder Form and Stable Metal Lactate Salt
EP1959995A1 (en) * 2005-11-30 2008-08-27 Can-Fite Biopharma Ltd. Therapeutic uses of a3 adenosine receptor antibodies
JP2009517063A (en) * 2005-11-30 2009-04-30 ピュラック バイオケム ビー．ブイ． Potassium lactate aqueous solution
EP1797773A1 (en) * 2005-12-16 2007-06-20 PURAC Biochem BV Aqueous potassium lactate solution
US8337867B2 (en) * 2008-02-08 2012-12-25 Purac Biochem B.V. Metal lactate powder and method for preparation
BR112012025943A2 (en) 2010-04-15 2017-07-25 Chromocell Corp compounds, compositions and methods for reducing or eliminating the bitter taste.
AU2011379360B2 (en) 2011-10-20 2016-08-11 Chromocell Corporation Compounds, compositions, and methods for reducing or eliminating bitter taste
DK2879524T3 (en) * 2012-08-01 2016-12-12 Purac Biochem Bv Laktatpulver and manufacturing method thereof
EP2754356A1 (en) 2013-01-15 2014-07-16 Purac Biochem N.V. Improved nisin production process
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WO2023161483A1 (en) 2022-02-28 2023-08-31 Purac Biochem B.V. Method for manufacturing sodium lactate solid particles and use thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2013104A (en) * 1933-01-30 1935-09-03 Du Pont Purification of lactic acid
NL7106959A (en) * 1971-05-21 1972-11-23 Dry,powdered sodium lactate - spray drying an optically-pure soln,used in aroma mixts
US3911141A (en) * 1973-11-22 1975-10-07 Nestle Sa Preparation of meat analogues
US4217344A (en) * 1976-06-23 1980-08-12 L'oreal Compositions containing aqueous dispersions of lipid spheres
US4511584A (en) * 1983-05-31 1985-04-16 Scm Corporation Particulate food acidulant
US7494684B2 (en) * 2001-10-08 2009-02-24 Purac Biochem B.V. Method for the preparation of a stable alkali metal lactate in powder form

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB395990A (en) * 1933-02-27 1933-07-27 Friedrich August Volkmar Klopf Improvements in the process of producing solid preparations of lactic acid
JP2502572B2 (en) * 1987-03-12 1996-05-29 株式会社 武蔵野化学研究所 Solid lactate salt and method for producing the same
FR2672295B1 (en) * 1991-01-31 1994-06-03 Roquette Freres THERMOFORMABLE COMPOSITIONS, THEIR PREPARATION PROCESS AND THEIR USE FOR OBTAINING THERMOFORMED ARTICLES.
JP3054998B2 (en) * 1994-07-06 2000-06-19 株式会社アマコス Process for producing powdered lactic acid and / or powdered lactate

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2013104A (en) * 1933-01-30 1935-09-03 Du Pont Purification of lactic acid
NL7106959A (en) * 1971-05-21 1972-11-23 Dry,powdered sodium lactate - spray drying an optically-pure soln,used in aroma mixts
US3911141A (en) * 1973-11-22 1975-10-07 Nestle Sa Preparation of meat analogues
US4217344A (en) * 1976-06-23 1980-08-12 L'oreal Compositions containing aqueous dispersions of lipid spheres
US4511584A (en) * 1983-05-31 1985-04-16 Scm Corporation Particulate food acidulant
US7494684B2 (en) * 2001-10-08 2009-02-24 Purac Biochem B.V. Method for the preparation of a stable alkali metal lactate in powder form

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
USMA U.S. Metric Association "Metric System Temperature" 1998-2012 pages 1-4 *
White et al. Journal of Food Technology 1966 vol. 1 pages 73-82. *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019068798A1 (en) 2017-10-05 2019-04-11 Purac Biochem B.V. Lactate powder and method for the preparation thereof
US11197494B2 (en) 2017-10-05 2021-12-14 Purac Biochem B.V. Lactate powder and method for the preparation thereof
CN110642702A (en) * 2019-09-10 2020-01-03 湖北壮美生物科技有限公司 Industrial preparation device of sodium lactate powder with high purity and low water content and corresponding preparation method

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ATE538082T1 (en) 2012-01-15

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