WO2007097626A1 - Preparing dried particles using a supercritical medium - Google Patents
Preparing dried particles using a supercritical medium Download PDFInfo
- Publication number
- WO2007097626A1 WO2007097626A1 PCT/NL2007/050077 NL2007050077W WO2007097626A1 WO 2007097626 A1 WO2007097626 A1 WO 2007097626A1 NL 2007050077 W NL2007050077 W NL 2007050077W WO 2007097626 A1 WO2007097626 A1 WO 2007097626A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- particles
- composition
- supercritical medium
- supercritical
- water
- Prior art date
Links
- 239000002245 particle Substances 0.000 title claims abstract description 88
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 238000000034 method Methods 0.000 claims abstract description 61
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 39
- 238000001035 drying Methods 0.000 claims abstract description 26
- 239000007788 liquid Substances 0.000 claims abstract description 20
- 239000007789 gas Substances 0.000 claims description 36
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 28
- 239000000839 emulsion Substances 0.000 claims description 21
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 14
- 235000013305 food Nutrition 0.000 claims description 14
- 239000003960 organic solvent Substances 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 12
- 238000001556 precipitation Methods 0.000 claims description 11
- 235000013361 beverage Nutrition 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- 238000005507 spraying Methods 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 8
- 239000008157 edible vegetable oil Substances 0.000 claims description 7
- 239000003925 fat Substances 0.000 claims description 7
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 235000012041 food component Nutrition 0.000 claims description 5
- 239000005417 food ingredient Substances 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- 150000001720 carbohydrates Chemical class 0.000 claims description 4
- 235000014633 carbohydrates Nutrition 0.000 claims description 4
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 238000010924 continuous production Methods 0.000 claims description 3
- 239000001272 nitrous oxide Substances 0.000 claims description 3
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 3
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 claims 1
- 229920001184 polypeptide Polymers 0.000 claims 1
- 239000000843 powder Substances 0.000 description 27
- 235000015116 cappuccino Nutrition 0.000 description 11
- 238000001694 spray drying Methods 0.000 description 10
- 239000012071 phase Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000004090 dissolution Methods 0.000 description 6
- 238000009434 installation Methods 0.000 description 6
- 235000013353 coffee beverage Nutrition 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 239000002274 desiccant Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 235000016213 coffee Nutrition 0.000 description 4
- 238000011437 continuous method Methods 0.000 description 4
- 238000005265 energy consumption Methods 0.000 description 4
- 239000008101 lactose Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 235000018102 proteins Nutrition 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000975 bioactive effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229910001867 inorganic solvent Inorganic materials 0.000 description 3
- 239000003049 inorganic solvent Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 235000000346 sugar Nutrition 0.000 description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000003795 desorption Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 238000004626 scanning electron microscopy Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000014347 soups Nutrition 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 239000005862 Whey Substances 0.000 description 1
- 102000007544 Whey Proteins Human genes 0.000 description 1
- 108010046377 Whey Proteins Proteins 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229940071162 caseinate Drugs 0.000 description 1
- 235000020140 chocolate milk drink Nutrition 0.000 description 1
- 235000020965 cold beverage Nutrition 0.000 description 1
- 235000021277 colostrum Nutrition 0.000 description 1
- 210000003022 colostrum Anatomy 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 231100000402 unacceptable toxicity Toxicity 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
- A23C1/00—Concentration, evaporation or drying
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L3/00—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
- A23L3/40—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by drying or kilning; Subsequent reconstitution
- A23L3/42—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by drying or kilning; Subsequent reconstitution with addition of chemicals before or during drying
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L3/00—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
- A23L3/40—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by drying or kilning; Subsequent reconstitution
- A23L3/46—Spray-drying
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F26—DRYING
- F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
- F26B3/00—Drying solid materials or objects by processes involving the application of heat
- F26B3/02—Drying solid materials or objects by processes involving the application of heat by convection, i.e. heat being conveyed from a heat source to the materials or objects to be dried by a gas or vapour, e.g. air
- F26B3/10—Drying solid materials or objects by processes involving the application of heat by convection, i.e. heat being conveyed from a heat source to the materials or objects to be dried by a gas or vapour, e.g. air the gas or vapour carrying the materials or objects to be dried with it
- F26B3/12—Drying solid materials or objects by processes involving the application of heat by convection, i.e. heat being conveyed from a heat source to the materials or objects to be dried by a gas or vapour, e.g. air the gas or vapour carrying the materials or objects to be dried with it in the form of a spray, i.e. sprayed or dispersed emulsions or suspensions
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- the invention relates to preparing particles from aqueous compositions and drying a composition, respectively.
- the invention further relates to thus prepared particles, and to the use of a supercritical medium.
- spray-drying is a conventional technique.
- spray-drying typically, wet emulsions or dispersions are sprayed under pressure in a spray tower and then contacted with hot air at a temperature of 140-300 0 C.
- spray-drying can cause problems as a result of a high thermal load of the product, which can lead to quality loss, in particular if the product contains a component which is heat-sensitive.
- problems can occur with the controllability of the product properties such as particle size distribution, form and/or solubility; there is the risk of dust explosions.
- the high energy consumption is a problem.
- the energy consumption is of the order of 3700 kJ per kg water which is removed.
- WO 99/17868 describes a method for preparing a powdery product from a liquid.
- the liquids to be treated are organic liquids or particle-forming material in an organic solvent.
- a gas is dissolved in the liquid under pressure.
- the pressure may be chosen within a wide range and may be below the supercritical pressure.
- the solution is expanded at a temperature below the critical temperature.
- a powdery auxiliary substance then the particles are formed.
- Use of the organic solvent makes this method unsuitable for the preparation of foods.
- WO 02/092213 relates to a method where an emulsion is dried using a supercritical liquid or a liquefied gas.
- the emulsion generally contains an organic solvent as the main solvent. Further, water is present.
- the choice of the organic solvent is critical with regard to obtaining a stable emulsion; it needs to be very soluble in the supercritical liquid or the liquefied gas and needs to be capable of extracting water along to the supercritical liquid or the liquefied gas. For extracting the water, it is important that the water content is sufficiently low. The importance of choosing the right organic solvent is a complicating factor.
- US-A 2003/215515 relates to conserving a bioactive material, including viruses and bacteria.
- a solution or suspension is prepared in the presence of a polyol.
- the solution or suspension is mixed with a high-pressure gas or a virtually supercritical liquid.
- a suspension of drops in the gaseous phase is prepared by reducing the pressure on the mixture.
- the drops are then dried using a subcritical drying gas.
- DE-A 19904990 relates to the preparation of solid nanoparticles from a dispersion using a gas brought under pressure.
- a solvent for the dispersion an alcohol is used, which may optionally contain a low content of water.
- the preparation of edible particles for foods is not described. It is an object of the invention to provide a new method with which particles can be prepared and a composition can be dried, respectively, in particular a method with which one or more of the problems mentioned herein are solved.
- an object of the invention is achieved by means of a method where, from an aqueous composition; water is separated from a particle-forming component by use of a specific medium.
- the invention relates to a method for preparing particles from an aqueous liquid composition which further contains a component to form the particles from, while the composition is contacted with a supercritical medium, so as to form the particles.
- the invention relates to a method for drying an aqueous composition, comprising removing water from the composition by contacting the composition with a supercritical medium.
- the aqueous composition is an emulsion, in particular an emulsion of oil and/or fat in an aqueous continuous phase.
- aqueous is at least understood to mean that more than 50 wt.% to 100 wt.%, in particular at least 75 wt.%, more in particular at least 90 wt.% or at least 95 wt.% of the above-mentioned phase consists of water.
- the emulsion contains at least one particle-forming component chosen from the group of carbohydrates and proteins.
- a supercritical medium is a substance at a temperature and pressure above the thermodynamically critical point. The critical point determines the conditions (temperature, pressure) at which the liquid phase in effect exists no longer. When a liquid is heated, the density decreases while the pressure and density of the vapor which is formed increase. Upon further heating, the densities of the liquid and vapor approach each other until the critical temperature is reached where the two densities are equal to each other and the liquid-gas (vapor) phase separation disappears.
- the critical point is the end point of a phase equilibrium curve, which separates two distinctive phases. At this point, the phases are no longer distinctive.
- the invention further relates to particles obtainable by means of a method according to the invention.
- particles according to the invention are powdery creamers, in particular cold soluble creamers, coffee powder, in particular cappuccino powder.
- the particles obtainable according to the invention are particles with a hierarchical structure.
- particles with a hierarchical structure are particles which are composed of different substances, in particular particles with one or more compartments of a first substance therein which are surrounded (encapsulated) by a second substance.
- an oil or fat is encapsulated by means of a method according to the invention.
- hierarchical particles in particular encapsulated oil and/or fat particles, can be produced by spraying an emulsion in a supercritical medium.
- demulsification see e.g. "A novel process for demulsification of water-in-erude oil emulsions by dense carbon dioxide", Zaki, Nael N.; Carbonell, Ruben G.; Kilpatrick, Peter K. Industrial & Engineering Chemistry Research (2003), 42(25), 6661-6672).
- Fig. 1 and Fig. 2 schematically show an installation with which a method according to the invention can be carried out;
- Fig. 3A shows a photograph taken with scanning electron microscopy of a cappuccino foamer according to the invention (Example 1);
- Fig. 3B shows a photograph taken with scanning electron microscopy of a cold soluble powder according to the invention (Example 2);
- Fig. 3C shows a photograph of a cold soluble powder according to the prior art.
- Fig. 4 shows the dissolution behavior of a number of powders prepared according to the invention and a powder according to the prior art.
- a method according to the invention is particularly suitable for preparing edible particles.
- “edible” is particularly understood to mean “suitable for human consumption", more in particular suitable for use in a food, including beverages, such as for instance in a dairy product, soup or a beverage.
- beverages are coffee, ice coffee, chocolate milk, fruit drinks or a cold drink.
- the invention relates to the preparation of a creamer, in particular for a soup or beverage, or a foamer, in particular for a beverage, such as cappuccino or another coffee drink provided with a layer of foam.
- a method according to the invention is favorable with a view to energy consumption.
- the water taken up by the supercritical medium can be removed by absorption to desiccants (zeolites) and/or condensing of the water from the supercritical medium.
- desiccants zeolites
- the desorption process of the desiccants can take place at relatively high temperatures.
- the residual heat released in the desorption process can be utilized again.
- the drying process can take place in more compact equipment, which reduces heat losses to the environment, compared with conventional drying.
- the total energy saving may be of the order of 500 kJ/kg.
- the method can be carried out in a smaller installation than a conventional spray-drying process.
- a smaller precipitation space drying tower
- equal capacity i.e. an equally large precipitation space has a higher capacity.
- the method according to the invention is very suitable to be carried out at a relatively low temperature, in particular a temperature of maximally 100 0 C. This makes the invention also excellently suitable for use on a composition containing a heat-sensitive component.
- the invention it is possible to form the particles in the absence of other solvents than water.
- the invention can be carried out without utilizing organic or inorganic solvents which are undesired, unsuitable or prohibited for use in products for human or animal consumption.
- the aqueous composition is essentially free of organic and inorganic solvents other than water and edible oils (such as vegetable and animal triglyceride oils).
- an edible oil is understood to mean an edible component which is allowed to be present in a product according to the invention. If present, the function of the edible oil is typically primarily to be a component of the particles being formed or dried. If desired, one or more other solvents than water may be present, in particular one or more other solvents which are permissible for a food or food ingredient in the concentration used. Typically, the weight ratio of the total content of organic solvents) and/or the total content of inorganic solvent(s) other than water up to the content of water in the liquid composition is less than 3:2 each, in particular less than 1:1, more in particular maximally 1:2, preferably maximally 1:4.
- the total content of solvents other than water and any edible oil present is typically less than 1:1, in particular maximally 1:3, preferably maximally 1:10, most preferably maximally 1:20, maximally 1:99 or maximally 1:1,000.
- the ratio is typically at least 1:1,000, at least 1:200 or at least 1:100.
- a method according to the invention further offers an advantage with regard to safety. Because a relatively low temperature is sufficient, there is little risk of explosion compared to a conventional spray-drying process. Not needing to use organic solvents also offers advantages in this respect.
- the invention also provides a product with a (more) homogeneous composition.
- Fig. 3C shows a cold soluble powder according to the prior art.
- lactose crystals are perceivable (1), which have not been taken up into the particles.
- saccharine powders such as lactose-containing powders, which are at least substantially free of free sugar crystals, such as lactose crystals.
- a particulate product according to the invention in one embodiment, it has been found that it is characterized by a relatively smooth surface and/or a high degree of roundness (sphericity) (see for instance Fig. 3C in comparison). Without wishing to be bound to any theory, it is suspected that the smoothness and/or high degree of roundness contribute to favorable flow properties. It has further been found that particles obtainable by means of the invention have a good solubility, in particular a better solubility (in particular a higher initial dissolution rate) in a solvent, such as water, than particles with a similar composition, prepared in a conventional spray-drying process (see for instance Fig. 4). It has further been found that a product obtainable by means of the invention has a slighter tendency to agglomeration and/or sticking than a conventional spray-dried product.
- a product obtainable by means of the invention contains a gas or a mixture of gases, such as nitrogen or air. Due to the manner of drying, it has been found that the gas is confined in the powder particle under pressure. Typically, here, it is found that some gas coming from the supercritical medium, such as CO2, is also present in the powder particles. The presence of this gas is determinable by means of a method described in Example 1, while a skilled person knows how to use an alternative for the CO2 sensor, for determining the presence of another gas than CO2.
- the content of such a gas based on the total gas content of the product, may be at least 10 wt.%, at least 20 wt.% or at least 40 wt.%.
- Essentially free is in particular understood to mean a content of less than 0.1 wt.%, based on the total weight of the particles, more in particular a content of less than 0.01 wt.%, still more particular a content below the detection limit, attainable with a conventional measurement technique such as GC. Where such contents are impermissible on the basis of legal provisions for a particular type of product, such as legislation in the field of foods, the content is typically below the maximum permissible value for such a product, for instance a food.
- the invention is further very suitable to be carried out in low-oxygen, in particular essentially oxygen-free, conditions, this in contrast with conventional spray-drying processes. This suppresses conventional oxidation processes.
- Low-oxygen is in particular understood to mean an oxygen concentration of less than 1 vol,% during the contact between the composition and the supercritical medium;
- essentially oxygen-free is in particular understood to mean an oxygen concentration of less than 0.1 vol.% during the contact between the composition and the supercritical medium.
- a method according to the invention may be carried out in a continuous drying installation, for instance in the installation schematically shown in Fig. 1. Therein, the composition, through line 1 using pump 2, and the supercritical medium, through line 4 using pump 3 are fed to nozzle 5.
- Fig. 2 shows a different installation in which the method can be carried out batchwise.
- the composition 1 is mixed with a gas 10, for instance nitrogen or CO2.
- a gas 10 for instance nitrogen or CO2.
- composition 1 with the gas 10 and the supercritical medium are led into the drying/precipitation space 6 through the nozzle 5.
- the supercritical medium is led to condensate tank 13 via cooler 12.
- the gas is drained off there, for instance to the atmosphere, while the particles remain on the bottom of the drying/precipitation space.
- aqueous composition a solution of particle-forming components in water or a suspension thereof can be used.
- the aqueous composition comprises an emulsion.
- the water content is preferably 10 to 50 wt.% based on the total weight of the composition.
- the weight ratio of water to particle-forming components may be chosen within the conventional limits, in particular within the range of 20 to 40%.
- the composition may be prepared artificially or be a natural product or a fraction thereof, such as milk, colostrum or whey.
- any component forming particles in the supercritical medium may be used.
- one or more components are used chosen from the group consisting of bioactive compounds.
- a method according to the invention is very suitable for preparing particles containing at least one component chosen from the group consisting of lipids (for instance fats), carbohydrates, proteins, peptides, acids, vitamins, flavorings and salts.
- the preferred components include oils and fats (such as hardened coconut fat); carbohydrates, such as sugars (such as glucose syrup and lactose), starch; emulsifiers (such as monostearate), salts of phosphates, peptides and proteins (such as caseinate).
- one or more auxiliary substances may be added, such as an auxiliary substance chosen from the group consisting of gases, emulsifiers, solid carrier materials (such as a sugar, starches, proteins and silica).
- a gas can be added to the composition.
- This gas can then be encapsulated during the formation of the particles.
- gases are, for instance, nitrogen, carbon dioxide and mixtures thereof.
- the quantity of gas is typically chosen in a ratio of gas to aqueous composition (without the gas) within the range of 0.01 to 4 w/w% or 0.1-4 w/w%.
- a supercritical medium in principle, any supercritical medium may be used in which the particle-forming component at least substantially does not dissolve. Typically, water does dissolve at least partly in the supercritical medium.
- Supercritical NH3 is also suitable, as are - particularly for applications outside food technology - supercritical organic hydrocarbons such as methane, ethane, ethane, propane, propene, n-butane, i-butane and n-pentane; alcohols such as benzyl alcohol, methanol, ethanol, (iso)propanol, (iso)butanol, halogenated compounds such as chlorotrifiuoromethane, monofluoromethane; cyclic hydrocarbons such as toluene, pyridine, cyclohexane, cyclohexanol and o-xylene.
- supercritical points thereof are known, for instance from EP 744922 Bl.
- Particle is understood to mean a material which is molecularly dissolved in neither the supercritical medium nor the water.
- the “particle” is wholly or partly solid or in gel form. Particles may be massive, hollow or porous.
- the particle may comprise a solid outside surrounding a gas or liquid.
- examples of such particles are, for instance, oil particles surrounded by a capsule from a solid material and cappuccino foamers, which particles comprise encapsulated gas, typically with a pressure higher than the atmospheric pressure.
- the particle may comprise a solid matrix and pores filled with a gas or a liquid.
- examples of such particles are, for instance, porous particles whose pores contain an oil and cappuccino foamers, where the pores are filled with a gas, typically with a pressure higher than the atmospheric pressure.
- the particle size may be set within wide limits.
- the volume-average particle size, as determined by means of laser diffraction, is within the range of 1 to 200 ⁇ m, more preferably within the range of 1 to 40 ⁇ m.
- Contacting aqueous composition and supercritical medium preferably comprises atomizing the composition.
- the spraying of at least the composition in a precipitation chamber, which space has a temperature and pressure above the critical point, is suitable.
- Spraying in the precipitation, chamber may take place from the bottom, the top, the side or a combination thereof.
- spraying from the top has been found very suitable.
- Very suitable is a method where the composition is mixed with supercritical medium and is then sprayed in a precipitation space, which space has a temperature and pressure above the critical point.
- Good results for spraying the composition in the precipitation space have particularly been achieved with a nozzle with two inlets and one outlet (a T-nozzle), such as a concentric nozzle for two liquids, where one of the inlets serves for the aqueous composition and the other for the supercritical medium.
- the temperature of the supercritical medium during the particle-forming contact with the composition may be chosen within a wide range. The temperature is minimally the temperature corresponding to the critical point of the supercritical medium. With a view to an increased drying capacity, the temperature is preferably at least 5°C above the critical point, more preferably at least 15°C above the critical point, most preferably at a temperature of at least 20 0 C above the critical point.
- the temperature is preferably maximally 100 0 C during the contact between the supercritical medium and the aqueous composition.
- Good results with regard to preventing or at least reducing thermal degradation reactions have been obtained with a temperature of maximally 80 0 C, in particular maximally 70 0 C, more in particular maximally 60 0 C.
- the pressure of the supercritical medium during the particle-forming contact with the composition may be chosen within a wide range. The pressure is minimally the pressure corresponding to the critical point of the supercritical medium. With a view to a favorable drying capacity, the pressure is preferably at least 25 bar above the critical point, more preferably at least 50 bar above the critical point, most preferably at least 75 bar above the critical point.
- the pressure is typically 500 bar during the contact between the supercritical medium and the aqueous composition, although higher pressures may be used if desired. Very suitable is a pressure of maximally 200 bar.
- the contact time of supercritical medium and the composition in supercritical conditions can be set within wide limits, depending on the type of process and the desired product. Typically, a contact time of 1200 seconds or less is sufficient, in particular for continuous preparation. The contact time is typically at least 1 second. For practical reasons, the contact time in supercritical conditions is typically maximally about 5 minutes, preferably maximally about 1 minute, in particular with continuous preparation.
- the particles have a particularly high integrity.
- Suitable separation steps comprise filtering and separation using a cyclone.
- the supercritical medium (whether or not transferred to the gas phase) can then be reused, after water has been removed therefrom.
- the removal of water preferably takes place by drying using a zeolite, silica or other solid desiccant. Because these desiccants can be used at a relatively low temperature, application thereof also offers energetic advantages.
- the invention will now be explained on the basis of the following examples, namely: cappuccino foamer and cold soluble powder.
- the invention further relates to a continuous method, comprising preparing particles from a liquid composition which further comprises a component to form the particles from, while the composition is contacted with a supercritical medium in continuous-process conditions under pressure.
- the invention further relates to a continuous method for drying aqueous composition, comprising the removal of water from the composition, while the composition is contacted with a supercritical medium in continuous-process conditions under pressure.
- a method as described hereinabove is particularly suitable.
- the particles are mixed with the supercritical medium under pressure, and then the mixture is sprayed, while the pressure may be lowered if desired.
- the temperature and pressure of the mixture prior to spraying are at or above supercritical conditions.
- the pressure and temperature in the precipitation space in which spraying takes place are preferably supercritical.
- a (conventional) nozzle may be used which is suitable for spraying compositions under the pressure in the supply line to the nozzle.
- Two cappuccino foamers were produced in an installation as shown in Fig. 2. Nitrogen gas was mixed with the emulsion in line prior to the dosing of the emulsion liquid to the drying vessel. The emulsion and CO2 were introduced into the drying vessel via a two-fluid nozzle. The process temperature of the drying vessel was 52°C and 6O 0 C, respectively, with the production of the cappuccino foamers.
- the pressure in the drying vessel was about 190 bar.
- the functionality of the powder was evaluated by means of a foaming test, where a quantity of powder was moistened with water and the height of the resulting foam layer was measured.
- Fig. 3A a SEM photograph of the thus produced cappuccino foamer is shown. It is visible that the powders formed are spherical and have a certain degree of homogeneity.
- the CO2 content was determined by mixing 0.1 gram of foamer with 1 ml of water in a tube with a capacity of 5 ml and determining the CO2 and the O2 content in the air in the tube with a CO2 and O2 sensor. From this, it can be calculated how much gas in total and how much CO2 is released from a powder.
- An emulsion (produced according to the classical agitation and homogenization technique) was sprayed with CCfoby a nozzle at a process temperature of 6O 0 C in a high-pressure vessel (175 bar). The process is schematically shown in Pig. 2.
- the emulsion and the CO2 were injected by means of a concentric two-fluid nozzle.
- a displacement pump pumped the emulsion into the vessel.
- the emulsion was at room temperature.
- the powder was collected on a filter in the vessel. SEM photographs were made of the produced cold soluble powders.
- the obtained powder is fairly liquid, that is to say that the emulsion drops are encapsulated well.
- the obtained cold soluble powder particles are round (Fig- 3B). This is a fundamental difference from the spray-drying technique where the produced powders are characterized by the presence of rough polydisperse and crystalline particles.
- the dissolution behavior of the produced cold soluble powders was characterized with the obscuration signal of Malvern laser diffraction measuring equipment.
- Fig. 4 shows the obscuration signal as a function of time.
- Fig. 4 shows that cold soluble powder according to the invention has a better dissolution behavior than the Vana Blanca 31 A produced through spray-drying process (Vana Blanca 31 A, available through Kievit, NL). The fact is that Fig. 4 shows a higher dissolution rate in the first seconds for the products according to the invention.
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- Engineering & Computer Science (AREA)
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- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Nutrition Science (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- Mechanical Engineering (AREA)
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Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2007218378A AU2007218378B2 (en) | 2006-02-23 | 2007-02-23 | Preparing dried particles using a supercritical medium |
JP2008556263A JP5019636B2 (en) | 2006-02-23 | 2007-02-23 | Process for the preparation of dried particles using a supercritical medium |
DK07715896.2T DK1996036T3 (en) | 2006-02-23 | 2007-02-23 | Preparation of dried particles with a supercritical medium |
CN2007800103773A CN101404901B (en) | 2006-02-23 | 2007-02-23 | Method for preparing dried particles using a supercritical medium |
US12/280,428 US20090258132A1 (en) | 2006-02-23 | 2007-02-23 | Preparing dried particles using a supercritical medium |
EP07715896A EP1996036B1 (en) | 2006-02-23 | 2007-02-23 | Preparing dried particles using a supercritical medium |
NZ571140A NZ571140A (en) | 2006-02-23 | 2007-02-23 | Preparing dried particles using a supercritical medium |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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NL1031224 | 2006-02-23 | ||
NL1031224A NL1031224C2 (en) | 2006-02-23 | 2006-02-23 | The preparation of dried particles using a supercritical medium. |
Publications (1)
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WO2007097626A1 true WO2007097626A1 (en) | 2007-08-30 |
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Family Applications (1)
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PCT/NL2007/050077 WO2007097626A1 (en) | 2006-02-23 | 2007-02-23 | Preparing dried particles using a supercritical medium |
Country Status (9)
Country | Link |
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US (1) | US20090258132A1 (en) |
EP (1) | EP1996036B1 (en) |
JP (1) | JP5019636B2 (en) |
CN (1) | CN101404901B (en) |
AU (1) | AU2007218378B2 (en) |
DK (1) | DK1996036T3 (en) |
NL (1) | NL1031224C2 (en) |
NZ (1) | NZ571140A (en) |
WO (1) | WO2007097626A1 (en) |
Cited By (6)
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EP2194795A1 (en) | 2007-09-28 | 2010-06-16 | Nestec S.A. | Instant drink powder |
EP2298286A1 (en) | 2009-09-18 | 2011-03-23 | Messer Italia S.p.A. | Process for dewatering of product powders and pharmaceutical compositions produced according to this process |
US20110097458A1 (en) * | 2008-03-12 | 2011-04-28 | Thomas Philip Imison | Foaming coffee composition |
FR3061949A1 (en) * | 2017-01-17 | 2018-07-20 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | METHOD AND DEVICE FOR DRYING FLUID BOTTLES UNDER PRESSURE |
US10492507B2 (en) | 2017-05-11 | 2019-12-03 | Cornell University | Process for improving shelf-life of fresh cut vegetables and food products produced thereby |
EP4190437A1 (en) | 2021-12-03 | 2023-06-07 | SiTec PharmaBio SL | Process and apparatus for the manufacture of solid microparticles |
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US7808140B2 (en) * | 2007-08-07 | 2010-10-05 | Baker Hughes Incorporated | ESP motor design |
US8043645B2 (en) | 2008-07-09 | 2011-10-25 | Starbucks Corporation | Method of making beverages with enhanced flavors and aromas |
WO2012162438A2 (en) * | 2011-05-24 | 2012-11-29 | Navitasmax, Inc. | Supercritical fluids, systems and methods for use |
UA108268C2 (en) * | 2013-05-23 | 2015-04-10 | METHOD OF OBTAINING POWDER PRODUCT AND INSTALLATION FOR ITS PERFORMANCE | |
KR20170087923A (en) | 2014-11-20 | 2017-07-31 | 바스프 에스이 | Process for preparing a porous inorganic powder |
JP7138837B2 (en) * | 2017-04-13 | 2022-09-20 | 池田食研株式会社 | Spray drying system and spray drying method |
CN107712042A (en) * | 2017-09-13 | 2018-02-23 | 安徽鑫泉米业有限公司 | A kind of multiple step format rice drying method |
CN110115345A (en) * | 2019-05-10 | 2019-08-13 | 成都大学 | A kind of nutrition digested tankage and preparation method thereof |
CN111530103B (en) * | 2020-05-08 | 2021-08-31 | 福建蓝烟新材料有限公司 | Supercritical spray drying method |
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- 2007-02-23 EP EP07715896A patent/EP1996036B1/en not_active Not-in-force
- 2007-02-23 CN CN2007800103773A patent/CN101404901B/en not_active Expired - Fee Related
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Cited By (14)
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EP2194795A1 (en) | 2007-09-28 | 2010-06-16 | Nestec S.A. | Instant drink powder |
EP2194795B1 (en) * | 2007-09-28 | 2015-01-07 | Nestec S.A. | Instant drink powder |
EP2689668A1 (en) | 2007-09-28 | 2014-01-29 | Nestec S.A. | Instant drink powder |
US20110097458A1 (en) * | 2008-03-12 | 2011-04-28 | Thomas Philip Imison | Foaming coffee composition |
US8968809B2 (en) * | 2008-03-12 | 2015-03-03 | Kraft Foods R & D, Inc. | Foaming coffee composition |
US9591863B2 (en) | 2008-03-12 | 2017-03-14 | Kraft Foods R & D, Inc. | Foaming coffee composition |
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EP4190437A1 (en) | 2021-12-03 | 2023-06-07 | SiTec PharmaBio SL | Process and apparatus for the manufacture of solid microparticles |
WO2023099713A2 (en) | 2021-12-03 | 2023-06-08 | Sitec Pharmabio, S.L. | Process and apparatus for the manufacture of solid microparticles |
Also Published As
Publication number | Publication date |
---|---|
JP2009536020A (en) | 2009-10-08 |
US20090258132A1 (en) | 2009-10-15 |
EP1996036A1 (en) | 2008-12-03 |
EP1996036B1 (en) | 2012-07-18 |
CN101404901B (en) | 2013-09-25 |
CN101404901A (en) | 2009-04-08 |
AU2007218378B2 (en) | 2012-03-01 |
JP5019636B2 (en) | 2012-09-05 |
DK1996036T3 (en) | 2012-10-22 |
NZ571140A (en) | 2010-09-30 |
AU2007218378A1 (en) | 2007-08-30 |
NL1031224C2 (en) | 2007-09-03 |
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