US20020012736A1 - Liquid coffee product - Google Patents
Liquid coffee product Download PDFInfo
- Publication number
- US20020012736A1 US20020012736A1 US09/343,263 US34326399A US2002012736A1 US 20020012736 A1 US20020012736 A1 US 20020012736A1 US 34326399 A US34326399 A US 34326399A US 2002012736 A1 US2002012736 A1 US 2002012736A1
- Authority
- US
- United States
- Prior art keywords
- coffee
- liquid
- product
- weight
- container
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 235000013353 coffee beverage Nutrition 0.000 title claims abstract description 94
- 239000007788 liquid Substances 0.000 title claims abstract description 54
- 239000007787 solid Substances 0.000 claims abstract description 35
- 235000021539 instant coffee Nutrition 0.000 claims abstract description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000001301 oxygen Substances 0.000 claims abstract description 13
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 13
- 150000001299 aldehydes Chemical class 0.000 claims description 12
- 150000002240 furans Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 9
- 235000021185 dessert Nutrition 0.000 claims description 6
- 238000012371 Aseptic Filling Methods 0.000 claims description 4
- 235000013361 beverage Nutrition 0.000 abstract description 19
- 241000723377 Coffea Species 0.000 description 64
- 238000000605 extraction Methods 0.000 description 20
- 239000000203 mixture Substances 0.000 description 14
- 239000000796 flavoring agent Substances 0.000 description 8
- 235000019634 flavors Nutrition 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- BYGQBDHUGHBGMD-UHFFFAOYSA-N 2-methylbutanal Chemical compound CCC(C)C=O BYGQBDHUGHBGMD-UHFFFAOYSA-N 0.000 description 6
- YGHRJJRRZDOVPD-UHFFFAOYSA-N 3-methylbutanal Chemical compound CC(C)CC=O YGHRJJRRZDOVPD-UHFFFAOYSA-N 0.000 description 6
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 6
- 125000005594 diketone group Chemical group 0.000 description 6
- 150000003233 pyrroles Chemical class 0.000 description 6
- 235000015123 black coffee Nutrition 0.000 description 5
- UUIQMZJEGPQKFD-UHFFFAOYSA-N n-butyric acid methyl ester Natural products CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 5
- JGFBQFKZKSSODQ-UHFFFAOYSA-N Isothiocyanatocyclopropane Chemical compound S=C=NC1CC1 JGFBQFKZKSSODQ-UHFFFAOYSA-N 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- PWLNAUNEAKQYLH-UHFFFAOYSA-N butyric acid octyl ester Natural products CCCCCCCCOC(=O)CCC PWLNAUNEAKQYLH-UHFFFAOYSA-N 0.000 description 4
- 235000003599 food sweetener Nutrition 0.000 description 4
- 239000003765 sweetening agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000001893 (2R)-2-methylbutanal Substances 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000006172 buffering agent Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 235000013336 milk Nutrition 0.000 description 3
- 239000008267 milk Substances 0.000 description 3
- 210000004080 milk Anatomy 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- VQKFNUFAXTZWDK-UHFFFAOYSA-N 2-Methylfuran Chemical compound CC1=CC=CO1 VQKFNUFAXTZWDK-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 241000533293 Sesbania emerus Species 0.000 description 2
- 235000009499 Vanilla fragrans Nutrition 0.000 description 2
- 244000263375 Vanilla tahitensis Species 0.000 description 2
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 2
- 239000008122 artificial sweetener Substances 0.000 description 2
- 235000021311 artificial sweeteners Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000011850 desserts Nutrition 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 235000012907 honey Nutrition 0.000 description 2
- 235000015243 ice cream Nutrition 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- TZMFJUDUGYTVRY-UHFFFAOYSA-N pentane-2,3-dione Chemical compound CCC(=O)C(C)=O TZMFJUDUGYTVRY-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical compound CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 235000007460 Coffea arabica Nutrition 0.000 description 1
- 240000007154 Coffea arabica Species 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- 125000000570 L-alpha-aspartyl group Chemical group [H]OC(=O)C([H])([H])[C@]([H])(N([H])[H])C(*)=O 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000008453 RTD coffee Nutrition 0.000 description 1
- 239000004376 Sucralose Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- YGCFIWIQZPHFLU-UHFFFAOYSA-N acesulfame Chemical compound CC1=CC(=O)NS(=O)(=O)O1 YGCFIWIQZPHFLU-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical class OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical class [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 238000000642 dynamic headspace extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical class [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- ZHNFLHYOFXQIOW-LPYZJUEESA-N quinine sulfate dihydrate Chemical compound [H+].[H+].O.O.[O-]S([O-])(=O)=O.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 ZHNFLHYOFXQIOW-LPYZJUEESA-N 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
- 235000019204 saccharin Nutrition 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000019408 sucralose Nutrition 0.000 description 1
- BAQAVOSOZGMPRM-QBMZZYIRSA-N sucralose Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 BAQAVOSOZGMPRM-QBMZZYIRSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 235000015041 whisky Nutrition 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F5/00—Coffee; Coffee substitutes; Preparations thereof
- A23F5/24—Extraction of coffee; Coffee extracts; Making instant coffee
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F5/00—Coffee; Coffee substitutes; Preparations thereof
- A23F5/24—Extraction of coffee; Coffee extracts; Making instant coffee
- A23F5/26—Extraction of water soluble constituents
- A23F5/262—Extraction of water soluble constituents the extraction liquid flowing through a stationary bed of solid substances, e.g. in percolation columns
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F5/00—Coffee; Coffee substitutes; Preparations thereof
- A23F5/24—Extraction of coffee; Coffee extracts; Making instant coffee
- A23F5/243—Liquid, semi-liquid or non-dried semi-solid coffee extract preparations; Coffee gels; Liquid coffee in solid capsules
Definitions
- This invention relates to a liquid coffee product which may be used as a refreshing beverage or topping.
- the invention also provides a method for the production of the liquid coffee product.
- Ready-to-serve coffee-based beverages are becoming increasing popular. Very often, these beverages contain milk solids or a whitener. Apart from providing a beverage having an appearance and taste similar to that of whitened coffee, the milk solids or whitener performs the function of masking some of the harsher flavors which may arise in ready-to-drink coffee beverages. When served chilled, however, coffee beverages which contain milk solids or a whitener are perceived to be less refreshing than black coffee beverages.
- Ready-to-serve black coffee beverages are available; especially in Asian markets. To avoid harsh flavors, however, these beverages contain less than 2% by weight of soluble coffee solids. Also, these beverages are usually heavily sweetened. Despite this, these beverages are often still characterized by harsher, dirty flavors and often do not provide very refreshing beverages when consumed chilled.
- this invention provides a ready-to-serve coffee product comprising an aseptically filled container, and a black, coffee containing liquid in the container; where the liquid has a fresh, clean taste.
- the liquid has a coffee solids concentration of above about 2% by weight; and more preferably above about 2.2% by weight.
- the liquid preferably has a ratio of aldehydes to furans of less than about 1:12.
- the black, coffee containing liquid is produced by a process comprising the steps of extracting coffee solids from roast and ground coffee at a draw-off ratio of less than about 3 to produce a coffee extract; and adjusting the concentration of soluble coffee solids in the coffee extract to less than about 5% by weight under oxygen-reduced conditions to provide the coffee containing liquid.
- the coffee containing liquid is aseptically filled into the container.
- this invention provides a method for providing a chilled coffee beverage, by the steps of providing an aseptically filled container containing a black, coffee containing liquid; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2 to 2.2% by weight; opening the container; and pouring the black, chilling the coffee containing liquid, such as by pouring it over ice particles from shaved or crushed ice.
- this invention provides a dessert topping product which comprises an aseptically filled container; and a black, coffee containing liquid in the container; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2% by weight.
- the coffee containing liquid may contain a sweetener and may contain flavors.
- This invention provides a liquid, black coffee product which has a fresh, clean taste with little objectionable bitter and harsh notes and which is in ready-to-serve form.
- the liquid coffee product may contain high amounts of soluble coffee solids; for example above 2% by weight.
- conventional black, liquid coffee products which are provided in ready-to-serve form have a soluble coffee solids content of about 1% and below. Concentrations of soluble coffee solids above about 1.5% by weight generally cannot be used in conventional products since the product would then have objectionable harsh and bitter notes.
- draw-off ratio means the ratio of the weight of the coffee extract removed from the extraction system to the weight of fresh coffee introduced into the extraction system.
- F o value means the equivalent time in minutes for a product held at a temperature of 121° C.
- Frans means compounds of the furan class including 2-methylfuran.
- Diketones means aroma compounds of the diketone class including 2,3-butanedione, and 2,3-pentanedione.
- Aldehydes means aroma compounds of the aldehyde class including isobutyraldehyde, 3-methyl-butanal, and 2-methyl-butanal.
- Pyrroles means compounds of the pyrrole class including 1-methyl-1H-pyrrole.
- ppm methyl butyrate means the calculated amount of a compound based upon the response factor of methyl butyrate.
- the liquid, black coffee product is produced by preparing a coffee extract.
- the coffee extract is prepared by subjecting roasted coffee beans to extraction under mild temperature conditions and using a low draw-off ratio.
- the roasted coffee beans are preferably ground prior to extraction. Any suitable beans or blends or beans may be used. Naturally, the better the bean quality, the better the product finally produced.
- the extraction may be carried out in a counter-current manner in one or more extraction vessels.
- Any suitable extraction vessels may be used; for example fixed bed reactors or continuous counter-current extractors.
- the choice and design of the vessels is a matter of preference and has no critical impact on the process.
- the extraction liquid may be caused to flow upward through the reactor or downward through the reactor, as desired.
- the extraction is conveniently carried out in a battery of fixed bed reactors connected such that extraction liquid may flow through them in series.
- the temperature of the extraction liquid used to extract the coffee solids is preferably below about 140° C.; and more preferably below about 120° C.
- the extraction liquid is conveniently hot water which may be, but need not necessarily be, deoxygenated. Coffee extract may also be used as the extraction liquid but this is less preferred.
- the draw-off ratio for the extraction is preferably less than about 3:1; more preferably less than about 2:1. It is surprisingly found that extraction using low draw-off ratios provides a coffee extract with a cleaner, fresher taste with fewer harsh notes.
- the coffee extract obtained will usually have a concentration of coffee solids in the range of about 8% to about 15% by weight.
- the coffee extract is maintained under reduced oxygen conditions. If desired, oxygen scavengers or antioxidants such as ascorbic acid may be added to the coffee extract. If it is necessary to store the coffee extract for any significant length of time, storage is best conducted under refrigerated conditions.
- the coffee extract is then formulated to provide the liquid coffee product.
- Ingredients such as sweeteners, flavors, buffers and the like may be added and the concentration of the soluble coffee solids reduced to the desired level.
- concentration of the soluble coffee solids will be adjusted to about 0.8% to about 3.5% by weight; more preferably about 2% to about 3% by weight.
- buffers include sodium and potassium bicarbonate, di-sodium and di-potassium phosphates, and sodium and potassium citrates. Various combinations of these buffers may also be used. The buffering system used will depend largely upon regulations in the various countries.
- suitable sweeteners include sugar, artificial sweeteners such as saccharin, cyclamates, acetosulfame, sucralose, L-aspartyl based sweeteners such as aspartame, and mixtures of sugar and artificial sweeteners.
- Suitable flavors which may be used include vanilla, bourbon, whisky, chocolate, and the like.
- the mixture of all components may then be subjected to homogenization if necessary.
- Oxygen-reduced conditions are preferably used during formulation of the liquid coffee product.
- the homogenized mixture is then preferably subjected to ultra high temperature (UHT) treatment.
- UHT ultra high temperature
- This may be accomplished by rapidly heating the mixture to a temperature above about 135° C.; for example to about 140° C. to about 150° C.
- This may be carried out in a suitable heat exchanger or by direct injection of steam into the liquid beverage mix.
- Suitable heat exchangers are plate heat exchangers, tubular heat exchangers and scraped surface heat exchangers; plate heat exchangers being particularly suitable.
- the mixture is held at the raised temperature for a time less than about 2 minutes but sufficient to provide a F o value of at least about 4.
- the mixture is conveniently held at the temperature for about 5 seconds to about 60 seconds.
- the F o value reached is preferably about 5 for products which will be cold vended.
- the F o value may be about 60 to 75.
- the treated mixture is then cooled to a temperature below about 60° C.; for example to less than about 40° C. This may be conveniently accomplished by using a suitable heat exchanger or by flash cooling the beverage. Again a plate heat exchanger is a particularly suitable heat exchanger. Flash cooling is especially suitable if the mixture was heated using direct injection of steam since the introduced steam may then be flashed off. Otherwise the increase in water content must be accounted for when preparing the mixture.
- suitable buffers and other additives may be may be added at this point.
- the liquid coffee product obtained is then aseptically filled into suitable containers.
- Standard aseptic filling machinery may be used.
- the containers are then sealed and stored.
- the aseptic filling is preferably carried out under reduced oxygen conditions.
- the liquid coffee product may be filled into suitable containers and then retorted. In this case, aseptic filling is not necessary.
- the filling is preferably carried out under reduced oxygen conditions. Standard filling and retorting machinery may be used.
- the products obtained are characterized by a fresh, clean taste with little of the harsh, bitter notes of most conventional ready-to-drink black coffee beverages. This is despite the fact that the product may contain raised levels of soluble coffee solids.
- the products may be consumed in many different ways. For example, the product may be poured over crushed or shaved ice to provide a refreshing beverage. Alternatively, the product may be used as a topping on desserts such as ice cream. Further, the product may be frozen and served as a dessert; especially when mixed with other frozen desserts or fresh whole milk.
- the products contain an advantageous ratio of aldehydes to furans of less than about 1:12; more preferably about 1:4 to about 1:10. It is believe that these characteristics have a favorable impact on the flavor of the products.
- aroma components are analyzed using gas chromatography and mass spectrometry.
- the aroma components are introduced into the gas chromatograph using a purge and trap method (no static headspace).
- the components separated in the gas chromatograph are detected using a mass spectrometer.
- the conditions of the gas chromatograph and mass spectrometer are as follows: Column Restek RTX-1 60 m ⁇ 0.25 mm ⁇ 1.0 ⁇ m Flow rate 20 ml/minute in He carrier gas Split ratio 20:1 Initial temperature 35° C. Initial hold time 1 minute Temperature increase rate 4° C. per minute Final temperature 190° C. Solvent delay 0 minutes Scan range 35 to 260 amu Electron energy 70 volts.
- An extraction battery of three fixed-bed extractors is used.
- the extractors are connected in series such that an extraction liquid may flow into a first extractor, to the second extractor, to the third extractor, and then out of the third extractor.
- the third extractor contains a charge of about 27 kg of fresh Arabica coffee grounds.
- the second extractor which was the third extractor in a previous cycle, contains partially extracted coffee grounds.
- the first extractor which was the second extractor in a previous cycle, contains the most extracted coffee grounds.
- the coffee extract is diluted to a coffee solids concentration of about 1% by weight under reduced oxygen conditions. Buffering agents are added and the coffee product is aseptically filled into packs containing about 250 ml. Reduced oxygen conditions are maintained.
- the coffee product has a fresh, clean taste with nutty and roasty notes.
- the coffee extract of example 1 is diluted to a coffee solids concentration of about 1% by weight under reduced oxygen conditions.
- Sugar (about 5% by weight) and buffering agents are added and the mixture is aseptically filled into packs containing about 250 ml. Reduced oxygen conditions are maintained.
- the coffee product has a fresh, clean taste with nutty and roasty notes.
- a pack produced according to example 1 is opened and the coffee product is then analyzed for diketones, aldehydes, furans, and pyrroles.
- the results are as follows: Product of Example 1 Compound Amount (ppm methyl butyrate) Diketones 0.2 Aldehydes 1.2 Furans 0.1 Pyrroles 0.08 Isobutyraldehyde 0.4 3-methyl-butanal 0.4 2-methyl-butanal 0.4
- a pack produced according to each of examples 1 and 2 is opened and the coffee product is then analyzed for acids.
- the acid break down of each coffee product is as follows: Product of example 1
- Product of example 2 Acid Amount mg/g Amount mg/g Quinate 1.37 1.09 Acetate 0.28 0.20
- Glycolate 0.12 0.10 Formate 0.14 0.11 Chloride 0.03 0.02
- Malate 0.11 0.09 Fumarate 0.01 0.02
- Sulfate 0.07 0.03 Oxalic 0.01 0.00
- the pH of each product is 5.9.
- the product of example 1 has a turbidity of 14.00 NTU while the product of example 2 has a turbidity of 32.00 NTU.
- a coffee extract is produced as described in example 1 and is diluted to a coffee solids concentration of about 2.5% by weight under reduced oxygen conditions. Buffering agents, sugar and honey are added and the coffee product is aseptically filled into packs containing about 250 ml. Reduced oxygen conditions are maintained.
- the coffee product has the following constituents: Substance Amount (weight %) Water 75.405 Sugar 18.93 Coffee solids 2.5 Honey 3.0 Sodium Bicarbonate 0.165
- the pH of the coffee product is about 6.2 to 6.4.
- the coffee product is poured over crushed ice to provide an iced beverage.
- the ice beverage has a fresh, clean taste with nutty and roasty notes.
- the beverage is refreshing with no perceivable bitter and harsh notes despite the high concentration of coffee solids.
- the coffee product of example 5 is poured over vanilla ice cream and presented to a taste panel as a dessert.
- the dessert is readily consumed with none of the panel finding objectionable bitter and harsh notes.
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Tea And Coffee (AREA)
- Non-Alcoholic Beverages (AREA)
Abstract
A ready-to-serve coffee product which provides a refreshing beverage or topping. The product is a black, coffee containing liquid in an aseptically filled container. The liquid has a fresh, clean taste and may contain more than 2% by weight of soluble coffee solids. The liquid is produced by extracting coffee solids from roast and ground coffee at a draw-off ratio of less than about 3. The concentration of soluble coffee solids in the coffee extract is then adjusted to less than about 5% by weight under oxygen-reduced conditions.
Description
- This invention relates to a liquid coffee product which may be used as a refreshing beverage or topping. The invention also provides a method for the production of the liquid coffee product.
- Ready-to-serve coffee-based beverages are becoming increasing popular. Very often, these beverages contain milk solids or a whitener. Apart from providing a beverage having an appearance and taste similar to that of whitened coffee, the milk solids or whitener performs the function of masking some of the harsher flavors which may arise in ready-to-drink coffee beverages. When served chilled, however, coffee beverages which contain milk solids or a whitener are perceived to be less refreshing than black coffee beverages.
- Ready-to-serve black coffee beverages are available; especially in Asian markets. To avoid harsh flavors, however, these beverages contain less than 2% by weight of soluble coffee solids. Also, these beverages are usually heavily sweetened. Despite this, these beverages are often still characterized by harsher, dirty flavors and often do not provide very refreshing beverages when consumed chilled.
- Therefore, there remains a need for a black, ready-to-serve, coffee-based product which has a fresh, clean flavor, and this invention addresses this need.
- Accordingly, in one aspect, this invention provides a ready-to-serve coffee product comprising an aseptically filled container, and a black, coffee containing liquid in the container; where the liquid has a fresh, clean taste. Preferably, the liquid has a coffee solids concentration of above about 2% by weight; and more preferably above about 2.2% by weight. Also, the liquid preferably has a ratio of aldehydes to furans of less than about 1:12.
- In another aspect, the black, coffee containing liquid is produced by a process comprising the steps of extracting coffee solids from roast and ground coffee at a draw-off ratio of less than about 3 to produce a coffee extract; and adjusting the concentration of soluble coffee solids in the coffee extract to less than about 5% by weight under oxygen-reduced conditions to provide the coffee containing liquid. Preferably, the coffee containing liquid is aseptically filled into the container.
- In yet another aspect, this invention provides a method for providing a chilled coffee beverage, by the steps of providing an aseptically filled container containing a black, coffee containing liquid; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2 to 2.2% by weight; opening the container; and pouring the black, chilling the coffee containing liquid, such as by pouring it over ice particles from shaved or crushed ice.
- In a further aspect, this invention provides a dessert topping product which comprises an aseptically filled container; and a black, coffee containing liquid in the container; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2% by weight. The coffee containing liquid may contain a sweetener and may contain flavors.
- Embodiments of the invention are now described by way of example only. This invention provides a liquid, black coffee product which has a fresh, clean taste with little objectionable bitter and harsh notes and which is in ready-to-serve form. The liquid coffee product may contain high amounts of soluble coffee solids; for example above 2% by weight. In general, conventional black, liquid coffee products which are provided in ready-to-serve form have a soluble coffee solids content of about 1% and below. Concentrations of soluble coffee solids above about 1.5% by weight generally cannot be used in conventional products since the product would then have objectionable harsh and bitter notes.
- In this specification, the term “draw-off ratio” means the ratio of the weight of the coffee extract removed from the extraction system to the weight of fresh coffee introduced into the extraction system.
- The term “F o value” means the equivalent time in minutes for a product held at a temperature of 121° C.
- In this specification, the term “Furans” means compounds of the furan class including 2-methylfuran.
- The term “Diketones” means aroma compounds of the diketone class including 2,3-butanedione, and 2,3-pentanedione.
- The term “Aldehydes” means aroma compounds of the aldehyde class including isobutyraldehyde, 3-methyl-butanal, and 2-methyl-butanal.
- The term “Pyrroles” means compounds of the pyrrole class including 1-methyl-1H-pyrrole.
- The term “ppm methyl butyrate” means the calculated amount of a compound based upon the response factor of methyl butyrate.
- The liquid, black coffee product is produced by preparing a coffee extract. The coffee extract is prepared by subjecting roasted coffee beans to extraction under mild temperature conditions and using a low draw-off ratio. The roasted coffee beans are preferably ground prior to extraction. Any suitable beans or blends or beans may be used. Naturally, the better the bean quality, the better the product finally produced.
- The extraction may be carried out in a counter-current manner in one or more extraction vessels. Any suitable extraction vessels may be used; for example fixed bed reactors or continuous counter-current extractors. The choice and design of the vessels is a matter of preference and has no critical impact on the process. Further, if fixed bed reactors are used, the extraction liquid may be caused to flow upward through the reactor or downward through the reactor, as desired. The extraction is conveniently carried out in a battery of fixed bed reactors connected such that extraction liquid may flow through them in series.
- The extraction is carried out under relatively mild conditions such that little or no hydrolysis of the coffee solids takes place. Therefore, the temperature of the extraction liquid used to extract the coffee solids is preferably below about 140° C.; and more preferably below about 120° C.
- The extraction liquid is conveniently hot water which may be, but need not necessarily be, deoxygenated. Coffee extract may also be used as the extraction liquid but this is less preferred.
- The draw-off ratio for the extraction is preferably less than about 3:1; more preferably less than about 2:1. It is surprisingly found that extraction using low draw-off ratios provides a coffee extract with a cleaner, fresher taste with fewer harsh notes.
- The coffee extract obtained will usually have a concentration of coffee solids in the range of about 8% to about 15% by weight. The coffee extract is maintained under reduced oxygen conditions. If desired, oxygen scavengers or antioxidants such as ascorbic acid may be added to the coffee extract. If it is necessary to store the coffee extract for any significant length of time, storage is best conducted under refrigerated conditions.
- The coffee extract is then formulated to provide the liquid coffee product. Ingredients such as sweeteners, flavors, buffers and the like may be added and the concentration of the soluble coffee solids reduced to the desired level. Ordinarily, the concentration of the soluble coffee solids will be adjusted to about 0.8% to about 3.5% by weight; more preferably about 2% to about 3% by weight.
- If used, examples of suitable buffers include sodium and potassium bicarbonate, di-sodium and di-potassium phosphates, and sodium and potassium citrates. Various combinations of these buffers may also be used. The buffering system used will depend largely upon regulations in the various countries.
- Further, if used, examples of suitable sweeteners include sugar, artificial sweeteners such as saccharin, cyclamates, acetosulfame, sucralose, L-aspartyl based sweeteners such as aspartame, and mixtures of sugar and artificial sweeteners.
- Suitable flavors which may be used include vanilla, bourbon, whisky, chocolate, and the like.
- The mixture of all components may then be subjected to homogenization if necessary. Oxygen-reduced conditions are preferably used during formulation of the liquid coffee product.
- The homogenized mixture is then preferably subjected to ultra high temperature (UHT) treatment. This may be accomplished by rapidly heating the mixture to a temperature above about 135° C.; for example to about 140° C. to about 150° C. This may be carried out in a suitable heat exchanger or by direct injection of steam into the liquid beverage mix. Suitable heat exchangers are plate heat exchangers, tubular heat exchangers and scraped surface heat exchangers; plate heat exchangers being particularly suitable.
- The mixture is held at the raised temperature for a time less than about 2 minutes but sufficient to provide a F o value of at least about 4. Depending upon the temperature to which the mixture is heated, the mixture is conveniently held at the temperature for about 5 seconds to about 60 seconds. The Fo value reached is preferably about 5 for products which will be cold vended. For products which will be hot vending, the Fo value may be about 60 to 75.
- The treated mixture is then cooled to a temperature below about 60° C.; for example to less than about 40° C. This may be conveniently accomplished by using a suitable heat exchanger or by flash cooling the beverage. Again a plate heat exchanger is a particularly suitable heat exchanger. Flash cooling is especially suitable if the mixture was heated using direct injection of steam since the introduced steam may then be flashed off. Otherwise the increase in water content must be accounted for when preparing the mixture.
- If needed and not added earlier, suitable buffers and other additives may be may be added at this point.
- The liquid coffee product obtained is then aseptically filled into suitable containers. Standard aseptic filling machinery may be used. The containers are then sealed and stored. The aseptic filling is preferably carried out under reduced oxygen conditions.
- If desired, although less preferable, the liquid coffee product may be filled into suitable containers and then retorted. In this case, aseptic filling is not necessary. The filling is preferably carried out under reduced oxygen conditions. Standard filling and retorting machinery may be used.
- The products obtained are characterized by a fresh, clean taste with little of the harsh, bitter notes of most conventional ready-to-drink black coffee beverages. This is despite the fact that the product may contain raised levels of soluble coffee solids. The products may be consumed in many different ways. For example, the product may be poured over crushed or shaved ice to provide a refreshing beverage. Alternatively, the product may be used as a topping on desserts such as ice cream. Further, the product may be frozen and served as a dessert; especially when mixed with other frozen desserts or fresh whole milk.
- It is found that the products contain an advantageous ratio of aldehydes to furans of less than about 1:12; more preferably about 1:4 to about 1:10. It is believe that these characteristics have a favorable impact on the flavor of the products.
- Specific examples of the invention are now described to further illustrate the invention. In the examples, aroma components are analyzed using gas chromatography and mass spectrometry. The aroma components are introduced into the gas chromatograph using a purge and trap method (no static headspace). The components separated in the gas chromatograph are detected using a mass spectrometer. The conditions of the gas chromatograph and mass spectrometer are as follows:
Column Restek RTX-1 60 m × 0.25 mm × 1.0 μm Flow rate 20 ml/minute in He carrier gas Split ratio 20:1 Initial temperature 35° C. Initial hold time 1 minute Temperature increase rate 4° C. per minute Final temperature 190° C. Solvent delay 0 minutes Scan range 35 to 260 amu Electron energy 70 volts. - All results are expressed in ppm methyl butyrate units.
- An extraction battery of three fixed-bed extractors is used. The extractors are connected in series such that an extraction liquid may flow into a first extractor, to the second extractor, to the third extractor, and then out of the third extractor. The third extractor contains a charge of about 27 kg of fresh Arabica coffee grounds. The second extractor, which was the third extractor in a previous cycle, contains partially extracted coffee grounds. The first extractor, which was the second extractor in a previous cycle, contains the most extracted coffee grounds.
- Water at about 104° C. is introduced into the first extractor as the extraction liquid. The draw-off ratio is about 1.7:1 to provide about 45 kg of coffee extract. The extraction yield is about 20% and the concentration of coffee solids is about 11% by weight. The coffee extract is held in a container sized such that little or no head-space is present.
- The coffee extract is diluted to a coffee solids concentration of about 1% by weight under reduced oxygen conditions. Buffering agents are added and the coffee product is aseptically filled into packs containing about 250 ml. Reduced oxygen conditions are maintained.
- The coffee product has a fresh, clean taste with nutty and roasty notes.
- The coffee extract of example 1 is diluted to a coffee solids concentration of about 1% by weight under reduced oxygen conditions. Sugar (about 5% by weight) and buffering agents are added and the mixture is aseptically filled into packs containing about 250 ml. Reduced oxygen conditions are maintained.
- The coffee product has a fresh, clean taste with nutty and roasty notes.
- A pack produced according to example 1 is opened and the coffee product is then analyzed for diketones, aldehydes, furans, and pyrroles. The results are as follows:
Product of Example 1 Compound Amount (ppm methyl butyrate) Diketones 0.2 Aldehydes 1.2 Furans 0.1 Pyrroles 0.08 Isobutyraldehyde 0.4 3-methyl-butanal 0.4 2-methyl-butanal 0.4 - A pack produced according to each of examples 1 and 2 is opened and the coffee product is then analyzed for acids. The acid break down of each coffee product is as follows:
Product of example 1 Product of example 2 Acid Amount mg/g Amount mg/g Quinate 1.37 1.09 Acetate 0.28 0.20 Glycolate 0.12 0.10 Formate 0.14 0.11 Chloride 0.03 0.02 Malate 0.11 0.09 Fumarate 0.01 0.02 Sulfate 0.07 0.03 Oxalic 0.01 0.00 Phosphate 0.07 0.07 Citrate 0.25 0.25 - The pH of each product is 5.9. The product of example 1 has a turbidity of 14.00 NTU while the product of example 2 has a turbidity of 32.00 NTU. These results indicate that the product are relatively clear.
- A coffee extract is produced as described in example 1 and is diluted to a coffee solids concentration of about 2.5% by weight under reduced oxygen conditions. Buffering agents, sugar and honey are added and the coffee product is aseptically filled into packs containing about 250 ml. Reduced oxygen conditions are maintained.
- The coffee product has the following constituents:
Substance Amount (weight %) Water 75.405 Sugar 18.93 Coffee solids 2.5 Honey 3.0 Sodium Bicarbonate 0.165 - The coffee product is then analyzed for diketones, aldehydes, furans, and pyrroles. The results are as follows:
Product of Example 5 Compound Amount (ppm methyl butyrate) Diketones 0.2 Aldehydes 1.2 Furans 0.1 Pyrroles 0.05 Isobutyraldehyde 0.4 3-methyl-butanal 0.4 2-methyl-butanal 0.4 - The pH of the coffee product is about 6.2 to 6.4. The coffee product is poured over crushed ice to provide an iced beverage. The ice beverage has a fresh, clean taste with nutty and roasty notes. The beverage is refreshing with no perceivable bitter and harsh notes despite the high concentration of coffee solids.
- The coffee product of example 5 is poured over vanilla ice cream and presented to a taste panel as a dessert. The dessert is readily consumed with none of the panel finding objectionable bitter and harsh notes.
Claims (16)
1. A ready-to-serve coffee product comprising an aseptically filled container; and a black, coffee containing liquid in the container; the liquid having a fresh, clean taste.
2. The product according to claim 1 in which the liquid has a coffee solids concentration of above about 2% by weight.
3. The product according to claim 1 which has a ratio of aldehydes to furans of less than about 1:12.
4. A ready-to-serve coffee product comprising an aseptically filled container; and a black, coffee containing liquid in the container; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2.2% by weight.
5. The product according to claim 4 which has a ratio of aldehydes to furans of less than about 1:12.
6. The product according to claim 4 in the form of a dessert topping.
7. A coffee product comprising a black, coffee containing liquid in a container; the liquid having a fresh, clean taste, and wherein the liquid is produced by a process comprising:
extracting coffee solids from roast and ground coffee at a draw-off ratio of less than about 3 to produce a coffee extract; and
adjusting the concentration of soluble coffee solids in the coffee extract to less than about 5% by weight under oxygen-reduced conditions to provide the coffee containing liquid.
8. The product according to claim 7 in which the coffee containing liquid is aseptically filled into the container.
9. The product according to claim 8 in which the coffee containing liquid is thermally treated at a temperature above 135° C. to obtain an Fo value of at least 4 prior to aseptic filling.
10. The product according to claim 7 which has a ratio of aldehydes to furans of less than about 1:12.
11. The product according to claim 7 in which the liquid has a coffee solids concentration of above about 2% by weight.
12. A method for providing a chilled coffee beverage, the method comprising the steps of providing an aseptically filled container containing a black, coffee containing liquid; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2% by weight; opening the container; and chilling the black, coffee containing liquid to form the chilled coffee beverage.
13. The method according to claim 12 , wherein the coffee containing liquid is chilled by pouring it over crushed or shaved ice.
14. A dessert topping product which comprises an aseptically filled container; and a black, coffee containing liquid in the container; the liquid having a fresh, clean taste and a concentration of soluble coffee solids above about 2% by weight.
15. The product according to claim 14 in which the liquid has a coffee solids concentration of above about 2.2% by weight.
16. The product according to claim 14 which has a ratio of aldehydes to furans of less than about 1:12.
Priority Applications (1)
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|---|---|---|---|
| US09/343,263 US6352736B2 (en) | 1998-07-23 | 1999-06-30 | Liquid coffee product |
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| US9390398P | 1998-07-23 | 1998-07-23 | |
| US09/343,263 US6352736B2 (en) | 1998-07-23 | 1999-06-30 | Liquid coffee product |
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| US20020012736A1 true US20020012736A1 (en) | 2002-01-31 |
| US6352736B2 US6352736B2 (en) | 2002-03-05 |
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| US09/343,263 Expired - Lifetime US6352736B2 (en) | 1998-07-23 | 1999-06-30 | Liquid coffee product |
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| US20050031761A1 (en) * | 2003-08-05 | 2005-02-10 | Donald Brucker | Methods of producing a functionalized coffee |
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| CN105828625A (en) * | 2013-12-20 | 2016-08-03 | 雀巢产品技术援助有限公司 | Liquid coffee beverage with improved aroma |
| KR20200041293A (en) * | 2017-08-18 | 2020-04-21 | 소시에떼 데 프로듀이 네슬레 소시에떼아노님 | Instant coffee drink and method for manufacturing the same |
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| ATE390851T1 (en) * | 2001-02-15 | 2008-04-15 | Procter & Gamble | COFFEE COMPOSITIONS WITH IMPROVED AROMATIC PROPERTIES AND METHOD FOR THE PRODUCTION THEREOF |
| US20030099752A1 (en) * | 2001-10-19 | 2003-05-29 | The Procter & Gamble Co. | Liquid coffee concentrates |
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- 1999-07-15 BR BRPI9912369-0A patent/BR9912369B1/en not_active IP Right Cessation
- 1999-07-15 CA CA002329830A patent/CA2329830C/en not_active Expired - Fee Related
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- 1999-07-15 RU RU2001105090/13A patent/RU2230457C2/en not_active IP Right Cessation
- 1999-07-15 ES ES99934706T patent/ES2233057T3/en not_active Expired - Lifetime
- 1999-07-15 AT AT99934706T patent/ATE283639T1/en active
- 1999-07-15 PT PT99934706T patent/PT1098570E/en unknown
- 1999-07-15 EP EP99934706A patent/EP1098570B1/en not_active Expired - Lifetime
- 1999-07-15 AU AU50383/99A patent/AU751223B2/en not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| DE69922377D1 (en) | 2005-01-05 |
| NO20010371D0 (en) | 2001-01-22 |
| RU2230457C2 (en) | 2004-06-20 |
| NZ508165A (en) | 2003-03-28 |
| BR9912369A (en) | 2001-04-17 |
| CA2329830C (en) | 2009-12-08 |
| US6352736B2 (en) | 2002-03-05 |
| ES2233057T3 (en) | 2005-06-01 |
| KR100572177B1 (en) | 2006-04-18 |
| BR9912369B1 (en) | 2011-04-19 |
| PT1098570E (en) | 2005-02-28 |
| EP1098570A1 (en) | 2001-05-16 |
| EP1098570B1 (en) | 2004-12-01 |
| NO20010371L (en) | 2001-01-22 |
| WO2000004789A1 (en) | 2000-02-03 |
| ZA200100614B (en) | 2002-01-22 |
| ATE283639T1 (en) | 2004-12-15 |
| CN1117523C (en) | 2003-08-13 |
| DK1098570T3 (en) | 2005-01-03 |
| CA2329830A1 (en) | 2000-02-03 |
| AU751223B2 (en) | 2002-08-08 |
| JP4388230B2 (en) | 2009-12-24 |
| CN1307451A (en) | 2001-08-08 |
| KR20010043765A (en) | 2001-05-25 |
| DE69922377T2 (en) | 2005-11-03 |
| JP2002521015A (en) | 2002-07-16 |
| NO320840B1 (en) | 2006-01-30 |
| AU5038399A (en) | 2000-02-14 |
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