WO1989003642A1 - Instant reconstitutable alcoholic beverages - Google Patents

Instant reconstitutable alcoholic beverages Download PDF

Info

Publication number
WO1989003642A1
WO1989003642A1 PCT/US1988/003781 US8803781W WO8903642A1 WO 1989003642 A1 WO1989003642 A1 WO 1989003642A1 US 8803781 W US8803781 W US 8803781W WO 8903642 A1 WO8903642 A1 WO 8903642A1
Authority
WO
WIPO (PCT)
Prior art keywords
water
alcohol
composition
beverage
volatile
Prior art date
Application number
PCT/US1988/003781
Other languages
French (fr)
Inventor
Mostafa K. Hamdy
Original Assignee
University Of Georgia Research Foundation, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by University Of Georgia Research Foundation, Inc. filed Critical University Of Georgia Research Foundation, Inc.
Publication of WO1989003642A1 publication Critical patent/WO1989003642A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12GWINE; PREPARATION THEREOF; ALCOHOLIC BEVERAGES; PREPARATION OF ALCOHOLIC BEVERAGES NOT PROVIDED FOR IN SUBCLASSES C12C OR C12H
    • C12G3/00Preparation of other alcoholic beverages
    • C12G3/005Solid or pasty alcoholic beverage-forming compositions

Definitions

  • the present invention relates to methods of making an instantly recon ⁇ titutable alcoholic beverage.
  • Dehydrated beverages would have a number of advantages, including decreased shipping and storage costs, decreased packaging cost, and possibly enhanced stability.
  • Other beverage industries have found methods for successfully dehydrating beverages such as coffee using freeze drying or spray drying.
  • Soft drink manufacturers use concentrates which are diluted and packaged at the distribution site. These concentrates are reconstituted prior to serving by the addition of carbonated water and other sources of C0 2 .
  • the present invention is a novel method for producing a dry reconstitutable alcoholic beverage wherein the alcoholic beverage is separated into a volatile fraction (the alcohol and other volatiles) and a non-volatile (water-soluble) fraction; the volatile fraction is reacted with a hydrolyzed starch compound, such as a maltodextrin of specific molecular weight, to yield a volatile powder, and the non-volatile fraction is dried to yield a dry water-soluble powder.
  • a hydrolyzed starch compound such as a maltodextrin of specific molecular weight
  • the alcoholic beverage is reconstituted by mixing the volatile powder and the water-soluble powder with water and carbonating.
  • the reconstituted beverage can be carbonated by addition of CO2 and water, by addition of soda water at about 0° to 15°C or by addition of citric acid, Na 2 C ⁇ 3 and water.
  • the final concentration of alcohol, the taste, and the extent of carbonation can be varied as desired by varying the relative ratio of volatile to non ⁇ volatile powders, the type and quantity of hydrolyzed starch compound and the method of carbonation.
  • alcoholic beverage Any type of alcoholic beverage, or alcohol, may be dehydrated and reconstituted according to the present invention.
  • Specific examples of alcoholic beverages are beer, wine, wine beverages and spirits.
  • Ethanol can also be dehydrated according to the present process for use in a variety of applications.
  • drying and reconstituting beer the beer is first degassed at room temperature to remove the carbon dioxide contained in the beverage.
  • the product obtained from fermentation prior to carbonation may also be used directly.
  • the degassed beverage is separated into the volatile (alcohol-containing) and non-volatile (water-soluble) fractions.
  • the separated fractions are then dried.
  • the environment, as well as the equipment utilized, should be clean and maintained free of contamination. Glass or stainless steel containers which are inert and do not leach any products harmful to the flavor or aroma of the beverage are preferred.
  • the preferred methods for drying the non ⁇ volatile fractions are spray drying and freeze drying. Freezing and drying equipment can be obtained commercially.
  • freeze-drying the non-volatile liquid fraction is frozen at a temperature of less than -20"C, preferably below -85°C, in a thin layer (generally less than about 4 cm) .
  • vacuum is applied to remove the liquid.
  • a reducing agent such as sodium ascorbate may be added in an amount of about 3-5 grams per liter of the beverage.
  • Other reducing agents known to those skilled in the art can also be used.
  • the non-volatile fraction is spray dried by spraying the liquid under freezing conditions, preferably in an inert gas atmosphere such as nitrogen to reduce oxidation.
  • Distillation equipment is required for the separation of the alcohol and other volatiles from the non-volatile fraction and subsequent recovery. This equipment is also commercially available.
  • degassed beer is rapidly reduced in volume to between about one-fourth to one-half of the original volume, preferably to about one-third of its original volume, by evaporating the alcohol and other volatile components and some of the water.
  • the pressure during this step should be reduced to and maintained at between about 300 and 400 mm Hg, preferably between about 300 and 340 mm Hg.
  • This process is performed at a temperature of between about 22° and 35°C, preferably between about 30° and 33°C.
  • This step can be performed with the use of flash evaporators or other devices capable of maintaining a desired combination of reduced pressure and temperature.
  • the water is then separated out of the evaporated alcohol-volatile-water mixture and the alcoholvolatile fraction collected by distillation.
  • the alcohol-volatile fraction, separated by distillation, is immobilized onto an inert, tasteless, porous, biocompatible support having high surface area.
  • the preferred group of compounds is hydrolyzed polysaccharides (starches) such as dextrin which are insoluble in alcohol and soluble in water.
  • starches polysaccharides
  • the advantages of this particular group of compounds are that they absorb the alcohol to yield an alcohol staturated dry powder which can be dissolved in the reconstituted water-soluble fraction, and that they are already well known and approved for use in the food industry.
  • a preferred compound is a maltrin polymer primarily containing dextrine, which is a degradation product of starch.
  • a still more preferred starch derivative is maltodextrine.
  • Other products having the required characteristics may be utilized.
  • the amount of alcohol that may be immobilized varies with the type of starch derivative used.
  • maltodextrin Maltrin M-100,500,600, Grain Product Co., Muscatine, Iowa.
  • Maltrin M-600 is capable of immobilizing about 0.91 g of 95% ethanol- volatiles mixture/g of Maltrin M-600.
  • 0.7g of 95% ethanol can be absorbed/g Maltrin M500 and 1.7g 95% ethanol can be absorbed/g Maltrin MIOO.
  • the immobilized alcohol- volatiles mixture should be kept in a sealed, moisture-proof container.
  • Plastic moisture-proof packages can be prepared using moisture barrier films (Cryovac Co. , Greenville, South Carolina) . Moisture- proofed glass containers may also be used.
  • the alcohol-volatiles fraction has been stabily preserved in such containers for greater than two years.
  • the solid alcohol-volatiles product can be compressed into tablet form, with or without the addition of carriers, antioxides, or other compounds. However, excessive pressure can result in the loss of the alcohol.
  • Freeze-drying or spray-drying is preferably conducted soon after the non-volatile fraction is separated for better results.
  • the length of time for drying of the nonvolatile fraction of the beverage may vary depending on whether freeze-drying or spray- drying is utilized.
  • the length of time for the drying step also depends on the volume and nature of the beverage. However, drying may be accomplished within about 24 to 48 hours in most cases.
  • the dried water-soluble fraction should also be stored in a tight container to minimize exposure to moisture and light.
  • the solid product is stable under these conditions in excess of three years.
  • This dry mix may also be compressed in the form of a tablet for easier storage and packaging.
  • the dried non-volatile fraction is mixed with the immobilized alcohol-volatiles fraction.
  • the proportion of the two fractions may vary broadly and in accordance with the flavor, aroma, alcohol and other characteristics which are desirable for a particular beverage.
  • a preferred proportion is that which yields between 1 and 3% of alcohol by weight for beer and 10 to 12% of alcohol for wine.
  • the mixture can be further combined with dry carbonated salts and water, soda water, or C0 2 to produce a reconstituted carbonated alcoholic beverage.
  • the soda water and the water should be cooled to between about 0° and 15°C before use, and preferably to between about 5° and 8 ⁇ C.
  • the volume of water or soda water added to the dry reconstitutable components varies in accordance with the desired final concentration of alcohol, aroma, and taste.
  • the present invention is further illustrated by the following non-limiting examples.
  • An immobilization support medium Dextrin MlOO or M500 was used. The amount of alcohol which can be immobilized onto this medium before historesis is observed determines which form is most useful.
  • the optimum mixture can be determined by adding various amounts of 95% ethanol to 10 g of the immobilization medium. Historesis occurs with MlOO when 18 g ethanol is added. 17 g ethanol is therefore considered • optimal (i.e., 1.7 g 95% ethanol/g MlOO). For comparison, only 7 g 95% ethanol can be immobilized per 10 g M500. Consequently, a relatively large amount of M500 is required which can alter the characteristic taste of the reconstituted beverage. In contrast, MlOO has a much higher alcohol capacity and can be effectively used in an amount which does not affect the taste of the reconstituted beverage.
  • Citric acid and Na C0 3 added in a 4:3 ratio, yield the best results for carbonation of the reconstituted beverage.
  • a preferred way to use dry ice is with airtight plastic packaging.
  • the powdered dry ice is first mixed with both the non ⁇ volatile fraction and the immobilized alcohol fraction. Liquid is added and the mixture is then sealed in impermeable plastic packages, for example, provided by Cryovac Corp. If too much dry ice is added to a beer mixture and packaged, the pouch can explode from the gas pressure.
  • the best results for this method are obtained using a device such as the Alcoa home beer dispenser.
  • the gallon keg is filled with the dehydrated non-volatile fraction, the immobilized alcohol, and water, up to a gallon, and then a 13.5 g C0 cartridge is inserted into the dispenser apparatus.
  • the C0 2 is absorbed into the beer.
  • the best C0 2 penetration occurs approximately 24 hours after the cartridge is installed.
  • the ingredients are mixed together with cold water 30 up to 355 ml and poured into the mini-keg.
  • the dispenser apparatus is attached and the C0 2 cartridge installed.
  • the whole keg apparatus is kept at 4°C in a refrigerator for several hours, allowing absorption of the C0 2 into the beer, (c) Beer from dehydrated beer tablets.
  • Dehydrated non-volatile beer fraction as described above, was compressed using a pharmaceutical press used for the manufacturing of pills. Tablets of varying sizes were reconstituted by the addition of water. This beer is free of alcohol and can be used as is or alcohol and carbonation can be added, as described above.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Alcoholic Beverages (AREA)
  • Non-Alcoholic Beverages (AREA)

Abstract

The present invention is a method and means for producing a dry reconstitutable alcoholic beverage wherein the alcoholic beverage is separated into a volatile fraction (the alcohol and other volatiles) and a non-volatile (water-soluble) fraction; the volatile fraction is immobilized on a hydrolyzed starch compound, such as a maltodextrin of specific molecular weight, to yield an alcohol-volatile powder, and the non-volatile fraction is dried to yield a dry water-soluble powder. The dry fractions, alone or in combination, can be pressed into tablets and/or packaged for later reconstitution. The alcoholic beverage is reconstituted by mixing the alcohol-volatile powder and the dry water soluble powder with water and carbonating. The reconstituted beverage can be carbonated by addition of CO2 and water, by addition of soda water at about 0° to 15°C, or by addition of citric acid, Na2CO3 and water.

Description

INSTANT RECONSTITUTABLE ALCOHOLIC BEVERAGES
BACKGROUND OF THE INVENTION The present invention relates to methods of making an instantly reconεtitutable alcoholic beverage. There has long been a need to have a method for dehydrating beer and other alcoholic beverages without detrimentally affecting their taste or storage properties. Dehydrated beverages would have a number of advantages, including decreased shipping and storage costs, decreased packaging cost, and possibly enhanced stability. There is also a need for a method of reconstituting the dehydrated alcoholic beverage which yields the desired amount of both alcohol and carbonation. Other beverage industries have found methods for successfully dehydrating beverages such as coffee using freeze drying or spray drying. Soft drink manufacturers use concentrates which are diluted and packaged at the distribution site. These concentrates are reconstituted prior to serving by the addition of carbonated water and other sources of C02. Other methods of carbonation are known. For example, U.S. Patent No. 3,965,273, issued in 1976 to Stahl, describes the carbonation of a non-alcoholic beverage with dried calcium carbonate dispersed within a matrix of water-soluble carbohydrates. U.S. Patent No. 3,939,289 to Hornyak and Stahl similarly provides a dry carbonation source for cola-like beverages prepared by cogrinding calcium carbonate and an anhydrous water-soluble non-toxic acid which is mixed with water, a sweetener and a flavoring. U.S. Patent No. 3,888,998 to Sampson and yte describes a method for retaining sufficient carbonation in a non¬ alcoholic beverage using a dry beverage mix and porous crystalline zeolite that absorbs 5% or more by weight of carbon dioxide.
Unfortunately, none of these methods can be used with an alcohol containing beverage without significantly altering the taste and amount of alcohol in the reconstituted beverage.
During the past 25 years numerous efforts have been made to create a usable dry alcoholic beverage mixture. For example, U.S. Patent No. 3,576,644, issued in 1971 to Anderson et al, describes a dry alcoholic beverage-forming composition of a particulate alkyl carbonate of calcium and a water- dispersible acidic flavoring agent. Unfortunately, products containing dried alcohol are unstable and suffer from a deterioration in taste.
It is therefore an object of the present invention to provide a concentrated alcoholic beverage product, particularly in dry form, which can be reconstituted without any deterioration of the flavor or the appearance of an undesirable aftertaste. It is a further object of the present invention to provide a method and means for stably storing alcohol in dry form for use in a variety of processes and applications. It is a still further object of the present invention to provide a method for carbonating a recon¬ stituted alcoholic beverage.
SUMMARY OF THE INVENTION The present invention is a novel method for producing a dry reconstitutable alcoholic beverage wherein the alcoholic beverage is separated into a volatile fraction (the alcohol and other volatiles) and a non-volatile (water-soluble) fraction; the volatile fraction is reacted with a hydrolyzed starch compound, such as a maltodextrin of specific molecular weight, to yield a volatile powder, and the non-volatile fraction is dried to yield a dry water-soluble powder. The dry powders can be pressed into tablets and/or packaged separately or in combination for later reconstitution.
The alcoholic beverage is reconstituted by mixing the volatile powder and the water-soluble powder with water and carbonating. The reconstituted beverage can be carbonated by addition of CO2 and water, by addition of soda water at about 0° to 15°C or by addition of citric acid, Na23 and water. The final concentration of alcohol, the taste, and the extent of carbonation can be varied as desired by varying the relative ratio of volatile to non¬ volatile powders, the type and quantity of hydrolyzed starch compound and the method of carbonation.
DETAILED DESCRIPTION OF THE INVENTION Any type of alcoholic beverage, or alcohol, may be dehydrated and reconstituted according to the present invention. Specific examples of alcoholic beverages are beer, wine, wine beverages and spirits. Ethanol can also be dehydrated according to the present process for use in a variety of applications. In one embodiment of the present process, drying and reconstituting beer, the beer is first degassed at room temperature to remove the carbon dioxide contained in the beverage. The product obtained from fermentation prior to carbonation may also be used directly.
The degassed beverage is separated into the volatile (alcohol-containing) and non-volatile (water-soluble) fractions. The separated fractions are then dried. The environment, as well as the equipment utilized, should be clean and maintained free of contamination. Glass or stainless steel containers which are inert and do not leach any products harmful to the flavor or aroma of the beverage are preferred.
The preferred methods for drying the non¬ volatile fractions are spray drying and freeze drying. Freezing and drying equipment can be obtained commercially. For freeze-drying, the non-volatile liquid fraction is frozen at a temperature of less than -20"C, preferably below -85°C, in a thin layer (generally less than about 4 cm) . Once the non¬ volatile fraction is completely frozen, vacuum is applied to remove the liquid. In order to minimize oxidation, a reducing agent such as sodium ascorbate may be added in an amount of about 3-5 grams per liter of the beverage. Other reducing agents known to those skilled in the art can also be used. Alternatively, the non-volatile fraction is spray dried by spraying the liquid under freezing conditions, preferably in an inert gas atmosphere such as nitrogen to reduce oxidation.
Distillation equipment is required for the separation of the alcohol and other volatiles from the non-volatile fraction and subsequent recovery. This equipment is also commercially available.
For example, degassed beer is rapidly reduced in volume to between about one-fourth to one-half of the original volume, preferably to about one-third of its original volume, by evaporating the alcohol and other volatile components and some of the water. The pressure during this step should be reduced to and maintained at between about 300 and 400 mm Hg, preferably between about 300 and 340 mm Hg. This process is performed at a temperature of between about 22° and 35°C, preferably between about 30° and 33°C. This step can be performed with the use of flash evaporators or other devices capable of maintaining a desired combination of reduced pressure and temperature. The water is then separated out of the evaporated alcohol-volatile-water mixture and the alcoholvolatile fraction collected by distillation. The alcohol-volatile fraction, separated by distillation, is immobilized onto an inert, tasteless, porous, biocompatible support having high surface area. The preferred group of compounds is hydrolyzed polysaccharides (starches) such as dextrin which are insoluble in alcohol and soluble in water. The advantages of this particular group of compounds are that they absorb the alcohol to yield an alcohol staturated dry powder which can be dissolved in the reconstituted water-soluble fraction, and that they are already well known and approved for use in the food industry. A preferred compound is a maltrin polymer primarily containing dextrine, which is a degradation product of starch. A still more preferred starch derivative is maltodextrine. Other products having the required characteristics may be utilized. The amount of alcohol that may be immobilized varies with the type of starch derivative used. In the case of maltodextrin (Maltrin M-100,500,600, Grain Product Co., Muscatine, Iowa). Maltrin M-600 is capable of immobilizing about 0.91 g of 95% ethanol- volatiles mixture/g of Maltrin M-600. 0.7g of 95% ethanol can be absorbed/g Maltrin M500 and 1.7g 95% ethanol can be absorbed/g Maltrin MIOO.
Since one of the key factors affecting the stability of the alcohol-volatiles fraction is environmental moisture, the immobilized alcohol- volatiles mixture should be kept in a sealed, moisture-proof container. Plastic moisture-proof packages can be prepared using moisture barrier films (Cryovac Co. , Greenville, South Carolina) . Moisture- proofed glass containers may also be used. The alcohol-volatiles fraction has been stabily preserved in such containers for greater than two years.
The solid alcohol-volatiles product can be compressed into tablet form, with or without the addition of carriers, antioxides, or other compounds. However, excessive pressure can result in the loss of the alcohol.
Freeze-drying or spray-drying is preferably conducted soon after the non-volatile fraction is separated for better results. The length of time for drying of the nonvolatile fraction of the beverage may vary depending on whether freeze-drying or spray- drying is utilized. The length of time for the drying step also depends on the volume and nature of the beverage. However, drying may be accomplished within about 24 to 48 hours in most cases.
The dried water-soluble fraction should also be stored in a tight container to minimize exposure to moisture and light. The solid product is stable under these conditions in excess of three years. This dry mix may also be compressed in the form of a tablet for easier storage and packaging.
The dried non-volatile fraction is mixed with the immobilized alcohol-volatiles fraction. The proportion of the two fractions may vary broadly and in accordance with the flavor, aroma, alcohol and other characteristics which are desirable for a particular beverage. A preferred proportion is that which yields between 1 and 3% of alcohol by weight for beer and 10 to 12% of alcohol for wine. The mixture can be further combined with dry carbonated salts and water, soda water, or C02 to produce a reconstituted carbonated alcoholic beverage. The soda water and the water should be cooled to between about 0° and 15°C before use, and preferably to between about 5° and 8βC. The volume of water or soda water added to the dry reconstitutable components varies in accordance with the desired final concentration of alcohol, aroma, and taste. The present invention is further illustrated by the following non-limiting examples.
The Reconstitution Of Beer Using Dehydrated Products.
When producing dehydrated beer, several ingredients must be removed from the beverage before or during drying, then added back into the dried powder during reconstitution. First, the C02 must be removed. The alcohol, volatiles and water must be removed. The alcohol must then be put into an immobilized form, and the water-soluble compounds dried. After addition of water to the dried powders, the C02 must be added back into the beer. The following examples detail methods for these processes as well as describe two different recipes for making reconstituted beer.
Alcohol Immobilization
An immobilization support medium. Dextrin MlOO or M500 was used. The amount of alcohol which can be immobilized onto this medium before historesis is observed determines which form is most useful. The optimum mixture can be determined by adding various amounts of 95% ethanol to 10 g of the immobilization medium. Historesis occurs with MlOO when 18 g ethanol is added. 17 g ethanol is therefore considered • optimal (i.e., 1.7 g 95% ethanol/g MlOO). For comparison, only 7 g 95% ethanol can be immobilized per 10 g M500. Consequently, a relatively large amount of M500 is required which can alter the characteristic taste of the reconstituted beverage. In contrast, MlOO has a much higher alcohol capacity and can be effectively used in an amount which does not affect the taste of the reconstituted beverage.
Methods of Carbonating the Reconstituted Beverage. (a) Addition of citric acid and Na23 to the dry mixture.
Citric acid and Na C03, added in a 4:3 ratio, yield the best results for carbonation of the reconstituted beverage. Higher concentrations of the citrate -
Na2C03 dry mixture alter the taste of the beverage. (b) Addition of powdered dry ice.
When dry ice and water are added directly to a reconstituted beverage, the dry ice floats on top and the gas escapes into the atmosphere.
A preferred way to use dry ice is with airtight plastic packaging. The powdered dry ice is first mixed with both the non¬ volatile fraction and the immobilized alcohol fraction. Liquid is added and the mixture is then sealed in impermeable plastic packages, for example, provided by Cryovac Corp. If too much dry ice is added to a beer mixture and packaged, the pouch can explode from the gas pressure. (c) Addition of C02 by use of a pressurized container with a C02 cartridge.
The best results for this method are obtained using a device such as the Alcoa home beer dispenser. The gallon keg is filled with the dehydrated non-volatile fraction, the immobilized alcohol, and water, up to a gallon, and then a 13.5 g C0 cartridge is inserted into the dispenser apparatus. The C02 is absorbed into the beer. The best C02 penetration occurs approximately 24 hours after the cartridge is installed.
Reconstitution and Carbonation of Dehydrated Beer (a) Beer recipe with Na2Cθ3 carbonation.
15 g dehydrated beer 17.1 g Ethanol immobilized-MlOO 1 g citric acid (anhydrous) 0.75 g Na C03 These ingredients are mixed together. Cold water 20 is added to 355 ml. After approximately 2 min, the beer is ready to drink. 17.1 g. of MlOO- ethanol yields an alcohol content of approximately
3.5% (v/v) . (b) Beer recipe with carbonation using an Alcoa Beer Dispenser
15 g dehydrated beer 17.1 g Ethanol immobilized-MlOO 0.2 g citric acid (anhydrous) 0.15 g Na2C03
The ingredients are mixed together with cold water 30 up to 355 ml and poured into the mini-keg. The dispenser apparatus is attached and the C02 cartridge installed. The whole keg apparatus is kept at 4°C in a refrigerator for several hours, allowing absorption of the C02 into the beer, (c) Beer from dehydrated beer tablets.
Dehydrated non-volatile beer fraction, as described above, was compressed using a pharmaceutical press used for the manufacturing of pills. Tablets of varying sizes were reconstituted by the addition of water. This beer is free of alcohol and can be used as is or alcohol and carbonation can be added, as described above.
Modifications and variations of the present invention will be obvious to those skilled in the art for the foregoing detailed description of the invention. These modifications and variations are intended to come within the scope of the appended claims.

Claims

I claim:
1. A method for producing a reconstitutable dry alcoholic beverage comprising: separating the alcohol-volatile fraction from the water-soluble fraction in an alcoholic beverage; removing the liquid from the separated water- soluble fraction; and absorbing the alcohol-volatile fraction onto an inert, porous, biocompatible polysaccharide material insoluble in alcohol and soluble in water.
2. The method of claim 1 further comprising degassing the alcoholic beverage before separating the two fractions.
3. The method of claim 1 further comprising selecting a hydrolyzed starch as the polysaccharide material.
4. The method of claim 1 wherein the alcohol- volatile fraction is separated from the water-soluble fraction by distillation.
5. The method of claim 1 wherein the liquid is removed from the water-soluble fraction by freeze- drying.
6. The method of claim 1 wherein the liquid is removed from the water-soluble fraction by spray- drying.
7. The method of claim 1 further comprising selecting the beverage from the group consisting of beer, wine, spirits and ethanol.
8. The method of claim 1 further comprising reconstituting the dry fractions.
9. The method of claim 8 wherein the fractions are reconstituted by the addition of water.
10. The method of claim 8 further comprising carbonating the reconstituted mixture.
11. The method of claim 10 wherein the fractions are reconstituted and carbonated by the addition of soda water.
12. The method of claim 10 wherein the mixture is carbonated by the addition of C02.
13. The method of claim 10 wherein the mixture is carbonated by adding citric acid and Na23 to the dry mixture.
14. The method of claim 10 wherein the reconstituted beverage is carbonated by adding an appropriate quantity of dry ice to the beverage and placing the mixture in a sealed container.
15. A dry alcohol composition comprising alcohol and a hydrolyzed starch derivative.
16. The composition of claim 15 further comprising the aromatic and volatile flavor components from an alcoholic beverage selected from the group consisting of beer, wine, wine beverages, and spirits.
17. The composition of claim 15 wherein said starch derivative is maltodextrin in granule form.
18. A composition for making a reconstituted beverage comprising a dry powder formed by removing the alcohol and volatile compounds from an alcoholic beverage and drying the water-soluble fractions.
19. The composition of claim 18 further comprising alcohol and volatile compounds isolated from an alcoholic beverage and immobilized on a hydrolyzed starch product.
20. The composition of claim 19 further comprising Na2C03 and citric acid.
21. The composition of claim 19 further comprising soda water.
22. The composition of claim 19 further comprising water.
23. The composition of claim 22 further comprising C02.
24. The composition of claim 19 further comprising a gas and liquid impermeable package.
PCT/US1988/003781 1987-10-26 1988-10-25 Instant reconstitutable alcoholic beverages WO1989003642A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11324187A 1987-10-26 1987-10-26
US113,241 1987-10-26

Publications (1)

Publication Number Publication Date
WO1989003642A1 true WO1989003642A1 (en) 1989-05-05

Family

ID=22348342

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1988/003781 WO1989003642A1 (en) 1987-10-26 1988-10-25 Instant reconstitutable alcoholic beverages

Country Status (2)

Country Link
AU (1) AU2717088A (en)
WO (1) WO1989003642A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996021722A1 (en) * 1995-01-13 1996-07-18 Krüger Gmbh & Co. Kg Alcoholic instant beverage mixture, its production and use
ES2121562A1 (en) * 1997-05-14 1998-11-16 Consejo Superior Investigacion Method for obtaining concentrated products for preparing sangrias and beverages flavoured with wine
KR100926027B1 (en) 2007-12-10 2009-11-11 조성제 Manufacturing method of carbonated water and carbonated water manufactured by the same
EP2815655A1 (en) * 2013-04-30 2014-12-24 Vasuta Gabor Laszlo Process for the production of a bottled drink mixture.
WO2017111698A1 (en) * 2015-12-24 2017-06-29 Red Horse Holdings Pte. Ltd. Instant alcoholic beverages and production thereof
WO2020215135A1 (en) * 2019-04-23 2020-10-29 Braghetto Neto Jose Virgilio Method for preparing an instant beer syrup, and products obtained
WO2022189294A1 (en) * 2021-03-09 2022-09-15 Van Gastel Anne Lievinus Preparation for preparing alcohol-containing aqueous beverages

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1541296A (en) * 1923-01-19 1925-06-09 William B Uihlein Dealcoholizing process
US2685783A (en) * 1950-06-09 1954-08-10 Ohio Commw Eng Co Method of and apparatus for dehydrating by freezing
US3956509A (en) * 1973-03-26 1976-05-11 General Foods Corporation Alcohol-containing dextrin powder
US4265920A (en) * 1977-03-19 1981-05-05 Douwe Egberts Koninklijke Tabaksfabriek, Koffiebranderijen En Theehandel B.V. Process for concentration of alcoholic beverages
US4702799A (en) * 1985-09-03 1987-10-27 Nestec S.A. Dryer and drying method

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1541296A (en) * 1923-01-19 1925-06-09 William B Uihlein Dealcoholizing process
US2685783A (en) * 1950-06-09 1954-08-10 Ohio Commw Eng Co Method of and apparatus for dehydrating by freezing
US3956509A (en) * 1973-03-26 1976-05-11 General Foods Corporation Alcohol-containing dextrin powder
US4265920A (en) * 1977-03-19 1981-05-05 Douwe Egberts Koninklijke Tabaksfabriek, Koffiebranderijen En Theehandel B.V. Process for concentration of alcoholic beverages
US4702799A (en) * 1985-09-03 1987-10-27 Nestec S.A. Dryer and drying method

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996021722A1 (en) * 1995-01-13 1996-07-18 Krüger Gmbh & Co. Kg Alcoholic instant beverage mixture, its production and use
ES2121562A1 (en) * 1997-05-14 1998-11-16 Consejo Superior Investigacion Method for obtaining concentrated products for preparing sangrias and beverages flavoured with wine
WO1998051775A2 (en) * 1997-05-14 1998-11-19 Consejo Superior De Investigaciones Cientificas Method for obtaining concentrated products for preparing sangrias and beverages flavoured with wine
WO1998051775A3 (en) * 1997-05-14 1999-02-18 Consejo Superior Investigacion Method for obtaining concentrated products for preparing sangrias and beverages flavoured with wine
KR100926027B1 (en) 2007-12-10 2009-11-11 조성제 Manufacturing method of carbonated water and carbonated water manufactured by the same
EP2815655A1 (en) * 2013-04-30 2014-12-24 Vasuta Gabor Laszlo Process for the production of a bottled drink mixture.
WO2017111698A1 (en) * 2015-12-24 2017-06-29 Red Horse Holdings Pte. Ltd. Instant alcoholic beverages and production thereof
CN108603152A (en) * 2015-12-24 2018-09-28 红马控股私人有限公司 Instant alcoholic beverage and its preparation
WO2020215135A1 (en) * 2019-04-23 2020-10-29 Braghetto Neto Jose Virgilio Method for preparing an instant beer syrup, and products obtained
WO2022189294A1 (en) * 2021-03-09 2022-09-15 Van Gastel Anne Lievinus Preparation for preparing alcohol-containing aqueous beverages

Also Published As

Publication number Publication date
AU2717088A (en) 1989-05-23

Similar Documents

Publication Publication Date Title
US5746937A (en) Oxygen absorbing composition
EP0030073B1 (en) Process for preparing carbonated beverages using coated charcoal and process for preparing the coated charcoal
ES2322227T3 (en) STABLE COFFEE CONCENTRATE SYSTEM.
JPH0414931B2 (en)
US4256773A (en) Brominated carbonaceous molecular sieve and method of use therefor
US3992493A (en) Beverage carbonation
US3936269A (en) Method of cold sterilization using frozen dimethyl dicarbonate
CZ156196A3 (en) Refreshing beverage
WO1989003642A1 (en) Instant reconstitutable alcoholic beverages
JP2018524420A (en) Deoxygenating polymer
US4695468A (en) Process for producing carbonated beverages
US3984580A (en) Method of containerizing fruit
US3979524A (en) Method of cold sterilization and preservation of food products using dimethyl dicarbonate
US4738857A (en) Shelf stable plastic packaged alcoholic beverage containing essential oils
US3193393A (en) Protecting packaged heat-processed aqueous food from oxygen deterioration
EP0037675B1 (en) Edible carriers for volatile components
CA1268457A (en) Amino sugar carbonating agents and their preparation
JPS61152268A (en) Powdery foamable, water-soluble and non-hygroscopic composition and its preparation
US4010285A (en) Concentrates for carbonated soft drinks
JP2001520030A (en) Method for maintaining carbonation in carbonated beverages and compositions therefor
JP5295617B2 (en) Method for producing concentrated composition for reduced beverage
JPH04349873A (en) Flavor preservative of raw material of palatable drink and preservation of flavor
CA1160893A (en) Process for preparing carbonated liquids with activated charcoal
AU2022235151A1 (en) Preparation for preparing alcohol-containing aqueous beverages
US3695896A (en) Preservation of volatile foodstuff flavours

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU JP KR

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE FR GB IT LU NL SE