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Publication numberUS3016336 A
Publication typeGrant
Publication dateJan 9, 1962
Filing dateSep 30, 1957
Priority dateSep 30, 1957
Publication numberUS 3016336 A, US 3016336A, US-A-3016336, US3016336 A, US3016336A
InventorsDon Scott, Hammer Frank E
Original AssigneeFermco Lab Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Deoxygenating method and product
US 3016336 A
Abstract  available in
Images(4)
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 3,016,336 DEOXYGENATHNG METHOD AND PRODUCT Don Scott and Frank E. Hammer, Chicago, lll., assignors to Fermco Laboratories, Inc., a corporation of Illinois No Drawing. Filed Sept. 30, 1957, Ser. No. 686,881 13 Claims. (Cl. 195-63) This invention relates to a method of protecting materials from the deleterious effects of free oxygen. More particularly, it relates to stabilization of articles of manufacture by removing free oxygen from association with the articles in relatively gas tight receptacles. Still more particularly, it relates to a dry pulverulent material comprising a solid carrier or base, glucose and a nonviable enzyme system having glucose oxidase activity, which may be intermingled with the dry product to be protected or merely associated therewith in an enclosed space but separate from the product to be protected by a gas permeable barrier.

Numerous types of industrial products are adversely afiected by free and uncombined oxygen. Oxygen reacts with these products with varying degrees of speed depending upon their chemical nature. The deleterious efiects of reaction with oxygen generally show up more rapidly in foods, solid or liquid, in which the oxidative deterioration results in impairment of flavor, alteration of color, destruction of vitamin content and the like. These reactions, with some types of food, can be so rapid that they occur within ten minutes of exposure and before complete processing can be efiected.

Slower but nevertheless destructive oxidative reactions occur in other fields, for example, the corrosion of metals. Materials of construction of the food containers themselves can be a problem. In the absence of suitable linings and coatings, the metal container may be attacked and become perforated. Other types of metallic objects, particularly those which are basically ferrous metal likewise require elaborate methods of protection during shipping and storage to prevent corrosion even though enclosed in plastic cocoons or other types of protective packaging.

Elimination of the oxygen from the receptacles or containers has been suggested for foods held in hermetically sealed cans. Oxygen elimination has been accomplished by enclosing in the container, but out of contact with the food, a moistureproof but oxygen permeable bag containing an aqueous dispersion of glucose and an enzyme system having glucose oxidase activity. Use of a moistureproof bag has been deemed necessary heretofore because an aqueous substrate is required for the enzymatic reaction to occur. The disadvantage of this separate bag has been that the films, which are sufficiently impermeable to moisture to hold the aqueous dispersion, also are very low in their gas or oxygen permeability and retard the oxygen reaction making oxygen removal a slow process.

When a material, normally subject to oxidative deterioration, can be isolated in a confined space or closed receptacle the amount of free oxygen present is limited to the amount absorbed in the material to be protected, the amount contained in the air about said material and that amount which may enter the confined space by permeation of the space walls or through leakage. In the normal course of industrial operation the total amount of oxygen to be removed for any particular type of packaging arrangement is determinable.

The present invention contemplates the use of a solid deoxygenating body comprising a solid carrier or base, preferably of porous character, having deposited therein and thereon a deoxygenating composition which is an enzyme system reactive with oxygen in the presence of substrate. If the elimination of by-products such as hy- 3,016,336 Patented Jan. 9, 1962 drogen peroxide, formed during oxidation, is necessary as an objectionable ingredient then additional enzymes may be introduced to convert the harmful by-product to a harmless one. For example, hydrogen peroxide may be eliminated by use of catalase.

Solid material useful as a carrier or base may vary as to chemical character, i.e., be organic or inorganic chemical compositions; and may vary as to physical character, i.e., particle size and porosity. Depending upon the use, the base may vary from a food ingredient to blocks of gypsum or pottery shards. When the deoxygenation is for the protection of dry foods adapted to either human or animal consumption, the carrier may be the entire food composition or a portion thereof or an ingredient of the food composition and be consumed therewith. In the case of animal foods, the carrier, preferably in a comminuted form, may be corn meal, corn cob, sugar can bagasse, beet pulp residue, sawdust and similar materials to give but a few examples.

Under other circumstances, the carrier plus enzyme may be intermingled with the food product subject to removal before use, by suitable separation means such as screening. When the deoxygenating body is to be separated from materials with which it is intermingled, the choice of particle size of the particulate body will be determined by the particle size of the material with which it is intermingled. The body may vary from a size requiring accurate screening for separation to a size manually removable. For example, the material subject to oxidative deterioration is a powder smaller than 20 mesh standard screen size, the carrie may vary from larger than 10 mesh size to a single unit having many square inches of surface area.

If the deoxygenating body or oxygen scavenger is to will at least in part be determined by the character of the restraining barrier. Under these circumstances, the barrier may be formed of suitable construction material, permeable to oxygen or nonpermeable material having perforations therein. Oxygen-permeable materials may be paper such as is used for enclosing tea, soluble coffee and the like or woven fabrics whose filament size and weave determine the interstitial voids. Barriers perforated to give oxygen access to the enzymatic composition usually are of a metallic or synthetic resin composition. Sizes of perforations usually are governed by particle size of the two materials being kept isolated. Carrier base particles utilized for formation of the deoxygenating bodies can always be chosen of a size to be retained by the perforations. The perforation sizes therefore are chosen to be such as to restrain the smaller particle size material from passing into the space reserved for the larger particle size material. In general, the particle size of the carrier can vary from blocks having many square inches of surface to comminuted material of a particle size all of which will pass through a or 200 mesh standard screen. The need for appreciable surface area for activity or reaction makes comminuted or pelletized carriers having a particle size in the range of 6 to 20 mesh preferable for many industrial uses. 7

In carrying out this invention, in a preferred embodiment thereof, a deoxygenating body is prepared by impregnating or otherwise depositing on and in the carrier or base an enzyme system containing glucose oxidase with or without catalase in a phosphate buffered aqueous solution containing glucose. In accordance with this in vention, glucose oxidase and a glucose substrate have been referred to as being important ingredients of the deoxygenating body. However, other oxid-ases or dehydrogenases that are capable of catalyzing a reaction between molecular oxygen and a specific substrate for the particular oxidase or dehydrogenase in an aqueous meair.

to increase the viscosity of the dispersion.

dium may also be employed. Thus, molecular oxygen will combine with (l) phenols and catcchols in the presence of tyrosinase; (2) aldehydes and purines in the presence of aldehyde-oxidase; (3) amino acids in the presence of amine acid oxidase; (4) uric acid in the presence of uricase; (5) mannose or galactose in the presence of mannose oxidase or galactose oxidase; (6) monoamines and diamines in the presence of amine oxidase and (7) unsaturated fatty acids in the presence of lipoxidase, and the like. 1

The enzyme preparation containing oxidase and catalase or other suitable deoxygenating mediums may be prepared in accordance with 'known procedures.

Moisture content of the carrier or base will be determined, in general, by its physical character, processing treatment and the like. In use, it is desired that the deoxygenating body have sufficient moisture to support enzyme activity but remain superficially in a dry state, i.e., the surface be devoid of free and unbound water which will cause agglomeration, balling and the like. Many of the otherwise suitable carriers contain insufiicient moisture. This deficiency may be corrected by direct addition of water or by adjustment of the water content of the oxidase dispersion which is deposited on the carrier. Clay materials such as fullers earth Will absorb their weight or more of water without becoming surface wetted to cause agglomeration. These clays therefore in powder or pelletized form provide an excellent ingredient for blending with other carriers to increase the moisture held by the surface dry carrier material. In general, it is preferred to maintain a moisture content for the deoxygenating body consisting of carrier and enzyme system of between about 7% and about 50% by weight. Subjecting the carrier, interpenetrated with aqueous disper sion of glucose-enzyme system, to vacuum treatment at temperatures lower than about 45 C. for periods of varying length provides means for control over the moisture content of the deoxygenating body. Moisture content within a closed receptacle must be kept sufficiently low not to permit diffusion of excessive amounts of water vapor to the dry product subject to oxidative deterioration. Where even the passage of small quantities of Water vapor out of the enzyme product are undesirable a desiccant may be used in conjunction with said deoxygenating body.

It will be apparent that the size of the deoxygenating body and the concentration of the various ingredients therein may be varied widely and will be dependent in part upon the amount of oxygen that must be removed from the enclosed space. The rate at which the enzyme material herein discussed will take up oxygen is a function of temperature, concentration of enzyme and active surface area of the deoxygenating body exposed to the The amount or" oxygen, that can be taken up in a given period of time, is limited by the amount of glucose to combine with the oxygen and the amount of butter present to neutralize the acid formed.

The deoxygenating body in its preferred form, in addition to a buffer, may contain preservatives and thickeners. Thickeners generally are used in an amount only The thickeners may comprise such substances as agar, gelatin, gums, carboxymethyl cellulose or inorganic material such as silica and the like. Suitable preservatives for the deoxygenating composition are sodium dehydroacetate, merthiolate and others which will stabilize against decomposition by microorganisms. Sufficient buffer, such as alkali metal phosphate, calcium carbonate, sodium acetate and the like is usually added to neutralize gluconic acid formed during the oxidation reaction. In this respect, sufiicient buffer is added to prevent the pH of the deoxygenating body from falling below about 3 to 4 since the enzyme system may be adversely affected under such acid conditions.

The invention, in a preferred embodiment thereof, is

carried out by preparing a phosphate buffered aqueous solution of glucose and sodium dehydroacetate. Enzyme system containing glucose oxidase and catalase is dispersed in the glucose solution. The resulting dispersion may contain 5 to 45% glucose, 0.3 to 0.6% sodium dehydroacetate and 0.1 to 1000 units per milliliter of glucose oxidase. In the absence of catalase, oxygen removal is faster. The hydrogen peroxide-catalase reaction produces 1 mole of oxygen for each 2 moles of H 0 decomposed. When catalase is present, the reaction formed oxygen must be removed by the glucose oxidase reaction as well as atmospheric oxygen. The dispersion is 0. 05 to 1.0 molar with respect to sodium acid phosphate and the pH is adjusted to between about 5.5 and 7.5. If 20 cc. of this type dispersion containing 500 glucose oxidase units per cc. is atomized onto 20 grams of carrier base having a particle size of +l0-20 mesh, this deoxygenating body, when introduced into a closed container of approximately 250 cc. gas capacity connected by suitable tubing to a mercury manometer, will produce in approximately 15 minutes vacuum of about 2 /2 inches, i.e., removal of about 40% of the oxygen in the enclosed space. In applications where comparatively large volumes of oxygen are to be removed the enzyme body should. be heavily buflfered to prevent pH drop. About /2 gram of gluconic acid is formed in removing 50 ml. of oxygen from the gas and use of 1 gram of calcium carbonate would be 'sufiicient to eifectively neutralize the gluconic acid formed. The total amount of glucose present must be at least equal to the stoichiornet'ric equivalent of the amount of oxygen to be removed;

In forming a deoxygenating body the carrier base may be interpenetrated or impregnated with enzyme composition by any suitable means. Atomizing accomplishes a Wide distribution of an aqueous dispersion over a large surface area. Where particle size is large and where capillary action is insuflicient to fully impregnate the carrier, the carrier may be impregnated by mixing with the aqueous system or su-bmerging it in the aqueous system, removing the wettcd solids from the aqueous system and subjecting it to' vacuum and then releasing the vacuum. By this means the pores and capillaries may be filled with the enzyme system and the surface of the carrier develops an outwardly dry appearance.

Among the carriers that may be used are vegetable fibers and residues, such as sawdust, ground corn cobs, woody ring of corn cobs, bark, bagasse and the like; glasses and plastics, such as striated Foamglass, polystyrene, polyurethane compositions, and the like; powdered and molded clay products, such as bentonite, fire clay, pottery shards and the like; natural and synthetic minerals, such as fullers earth, asbestos, dolomite, calcium silicate and the like; inorganic salts, such as calcium carbonate, alumina, titanium oxide and the like; porous abrasives, such as pumice, talc, vermiculite and the like; animal by-products, such as leather flour, bone meal and the like; cereal grains in whole or comrninuted form, such as wheat, barley, rice, corn and the like.

The invention will be more fully understood from the following examples:

Example 1 300 grams of glucose hydrate, 8 grams of sodium dehydroacetate and 178 grams of disodium phosphate duohydrate were dissolved in 1 liter of water to form a buffer solution. ml. of this buffer solution were mixed with 150 ml. of dilute glucose oxidase solution Example 2 A 150 ml. portion of the buffer solution prepared in Example 1 was mixed with 500 grams of a composition consisting of 400' grams of 40/60 mesh ground woody ring of corn cobs and 100 grams of calcium carbonate. 40 grams of the deoxygenating body were sealed in each of a number of No. 2 size cans. Into half of the cans, prior to sealing, were placed beakers containing a C absorber. The cans were hermetically sealed. The following day the cans were punctured. Cans which did not contain a C0 absorbent showed no vacuum since the evolution of CO from the carbonate produced a gaseous replacement volume-wise for the oxygen taken up in the glucose-enzyme reaction. Cans containing a C0 absorbent showed a vacuum of 5.5 inches of mercury measured by a manometer.

Example 3 A 20 m1. portion of the buffer solution prepared in Example 1 was mixed with 0.2 m1. of dilute glucose oxidase solution containing approximately 60 units per ml. of glucose oxidase and approximately 20 units per ml. of catalase. This aqueous dispersion of enzyme was mixed with 29 grams of comminuted woody ring of corn cobs. 16 grams of the deoxygenating composition consisting of base plus dispersion of enzyme contained only about 2.5 units of glucose oxidase and about 1 unit of catalase. 2, 8 and 16 gram portions of the deoxygenating body were sealed in 500 ml. Erlenmeyer flasks. After 16 hours the readings on mercury vacuum manometers were 0.2, .9 and 1.8 cm., respectively. After 36 hours the vacuum readings were 0.4, 1.3 and 3.2, respectively.

Example 4 A glucose bufier solution was prepared in the manner described in Example 1 having a composition consisting of 7.5% glucose, 0.4% sodium dehydroacetate. The glucose solution was adjusted to 0.25 molar phosphate concentration with disodium phosphate and phosphoric acid giving the solution a pH of approximately 6.5. 80 mls. of the butter solution were mixed with 1.8 mls. of enzyme solution containing approximately 750 units per ml. of glucose oxidase and approximately 400 units per ml. of catalase. This dispersion was mixed with 40 grams of expanded vermiculite. The deoxygenating composition was placed in bags made up of heat-scalable paper. These bags were then placed in glass flasks which were sealed and secured to vacuum gauges. At the end of 24 hours the gauge showed 2 inch vacuum. At the end of 48 hours the gauge showed 4.3 inches of vacuum indicating removal of a substantial portion of the oxygen.

Example 5 A 20 ml. portion of the buffer solution prepared in Example 1 was mixed with 2.0 ml. of dilute glucose oxidase solution containing 60 units per ml. of glucose oxidase and approximately 20 units per ml. of catalase. This aqueous dispersion of enzyme Was mixed with 29 grams of comminuted woody ring of corn cobs of 50/80 mesh particle size.

1 part by weight of this oxygen scavenger is mixed with 250 parts by weight of prepared guinea pig feed and the intermingled material pelletized by compression.

Pellets of feed were deposited in multi-wall bags and after storage, analysis for ascorbic acid showed excellent retention of ascorbic acid in an unoxidized state.

Example 6 A ml. portion of the bufier solution prepared in Example 1 was mixed with 2. 0 ml. of dilute glucose oxidase solution containing 60 units of glucose oxidase per ml. This aqueous dispersion of enzyme was mixed with 29 grams of fullers earth. The resultant mixture was packaged in heat-sealing tea bag stock. This fullers earth base scavenger was placed in 500 ml. Erlenmeyer flask attached to mercury manometer. After 24 hours the manometer showed four inches of vacuum.

Example 7 A 6.3 ml. portion of the butter solution prepared in Example 1 was mixed with 0.7 ml. dilute enzyme solution containing 60 units per ml. of glucose oxidase. This was then injected into a heat-sealed tea bag containing nine grams of whitepine sawdust of 60/80 mesh particle size. Upon manipulation of bag and contents, the free liquid was taken up by the carrier. One tea bag, thus produced, was enclosed in a 500 cc. container. After 24 hours, the container showed approximately 4 inches vacuum as measured by a mercury manometer.

It will be seen that means have been provided for removing uncombined oxygen from the interior of closed containers by utilizing a deoxygenating body with the packaged product. The term packaged product used herein is not intended to be restricted to anhydrous products but is intended to mean commercially dry or dehydrated products which may be used to designate powdered, granulated, granular or concentrated materials or nonaqueous materials or water-containing materials to which it is undesirable to add enzyme directly.

By the use of this invention no special means are required to evacuate or flush air from the package prior to closure' If the container is sealed with enclosed or entrapped air, the oxygen is gradually removed from such air by the reaction converting glucose to gluconic acid. Care should be exercised not to expose the deoxygenating body to atmospheric oxygen for extended periods prior to scaling the container because in the presence of sufficient moisture the body may be rendered ineffective for the intended purposes.

Although the invention has been described in connection with specific embodiments thereof, it will be understood that these are not to be regarded as limitations upon the scope of the invention except insofar as included in the accompanying claims.

We claim:

1. The method of preparing a deoxygenating body capable of removing free oxygen from closed receptacles containing moisture in amounts incapable of activating glucose-oxidase enzyme compositions which comprises interpenetrating particulate carrier material with an aqueous dispersion of substrate and an enzyme system reactive with oxygen in the presence of said substrate to form a deoxygenating body, the water content of said dispersion and said carrier base being such that the water is absorbed and the deoxygenating body outer surface is substantially free of unbound moisture.

2. The method of preparing a deoxygenating body capable of removing free oxygen from closed receptacles containing moisture in amounts incapable of activating glucose-oxidase enzyme, compositions which comprises impregnating particulate carrier with an aqueous dispersion of glucose and a nonviable enzyme system having glucose oxidase activity to form a deoxygenating body, the water content of said dispersion and said particulate carrier being such that the water is absorbed and the deoxygenating body outer surface is substantially free of unbound moisture.

3. The method of preparing a deoxygenating body capable of removing free oxygen from closed receptacles which comprises impregnating particulate carrier with an aqueous dispersion of glucose and a nonviable enzyme system having glucose oxidase activity to form a deoxygenating body, the water content of said dispersion and said particulate carrier being such that the surface is substantially free of unbound water when the water is absorbed in quantities constituting between about 7% and 50% by weight.

4. The method of preparing a deoxygenating b'ody capable of removing free oxygen from closed receptacles containing moisture in amounts incapable of activating glucose oxidase enzyme compositions which comprises impregnating particulate carrier with an aqueous dispersion of glucose and a nonviable enzyme system having glucose oxidase activity to form a deoxygenating body, the water content of said dispersion and said particulate carrier being such that the water is absorbed, and heating said deoxygenating body to a temperature below 45 C. to render the outer surface of the impregnated particulate solid dry.

5. A deoxygenating body comprising a solid carrier for enzyme, a deoxygenating composition interpenetrated into said solid carrier, said deoxygenating composition comprising substrate, an enzyme system reactive with oxygen in the presence of said substrate and water sufficient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

6. A deoxygenating body comprising a solid carrier for enzyme, a deoxygenating composition interpenetrated into said solid carrier, said deoxygenating composition comprising glucose, an enzyme system having glucose oxidase activity and water sufficient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

7. A deoxygenating body comprising comminuted corn cobs interpenetrated with deoxygenating composition comprising substrate, an enzyme system reactive with oxygen in the presence of said substrate and water sufficient to support oxidase activity whilethe outer surface of said carrier remains substantially free of unbound water.

8. A deoxygenating body comprising comminuted woody ring of corn cobs interpenetrated with deoxygenating composition comprising substrate, an enzyme system reactive with oxygen in the presence of said substrate and water sufiicient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

9. A deoxygenating body comprising fullers earth interpenetrated with deoxygenating composition comprising substrate, an enzyme system reactive with oxygen in the presence of said substrate and water sufiicient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

10. A deoxygenating body for use in closed receptacles comprising a solid carrier for enzyme, a deoxygenating &

composition interpenetra ted into said solid carrier, said d'eoxygenating composition comprising glucose, buttering ingredient, a nonviable enzyme system having glucose oxidase activity and water sufficient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

- 11. A deoxygenating body for use in closed receptacles comprising a solid carrier for enzyme, a deoxygenating composition interpenetrated into said solid carrier, said deoxygenating composition comprising glucose, disodium phosphate, a nonviable enzyme system having glucose oxidase activity and water sufficient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

12. A deoxygenating body for use in closed receptacles comprising a mixture of particulate carrier solids and calcium carbonate, a deoxygenating composition interpenetrated into said mixture, said deoxygenating composition comprising glucose, buffering ingredient, nonviable enzyme having glucose oxidase activity and water suflicient to support oxidase activity while the outer surface of said carrier remains substantially free of unbound water.

13. A deoxygenating body for use in closed receptacles comprising a mixture of particulate carrier solids and calcium carbonate, a deoxygenating composition interpenetrated into said mixture, said deoxygenating composition comprising glucose, disodium phosphate, and nonviable enzyme having glucose oxidase activity and water sufiicient to support oxidase activity While the outer surface of said carrier remains substantially free of unbound water.

References Cited in the file of this patent UNITED STATES PATENTS 1,679,543 Rector Aug. 7, 1928 2,072,955 Lunt Mar. 9, 1937 2,326,306 Pfannmuller a Aug. 10, 1943 2,482,724 Baker Sept. 20, 1949 2,733,145 Karr Jan. 31, 1956 2,758,932 Scott Aug. 14, 1956 2,765,233 Sarett et a1. Oct. 2, 1956 2,825,651 Sepulveda Mar; 4, 1958 FOREIGN PATENTS 553,991 Great Britain June 15, 1943

Patent Citations
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US1679543 *Oct 10, 1922Aug 7, 1928Rector Tenney Company IncPreserved-food product and process
US2072955 *Nov 16, 1933Mar 9, 1937Flodden Lunt William RichardMethod of treating food for human consumption
US2326306 *Feb 16, 1939Aug 10, 1943Wallerstein Co IncProteolytic bating composition
US2482724 *Jul 22, 1944Sep 20, 1949Ben L SarettDeoxygenation process
US2733145 *Jan 31, 1956 Corn cob absorbent and method of
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Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3169068 *Sep 12, 1962Feb 9, 1965Felix BlochPreservative of oxygen-labile substances, e.g., foods
US4299719 *Oct 23, 1979Nov 10, 1981Mitsubishi Chemical Ind., Ltd.Deoxidizer
US4414334 *Aug 7, 1981Nov 8, 1983Phillips Petroleum CompanyOxygen scavenging with enzymes
US4551431 *Apr 21, 1983Nov 5, 1985Phillips Petroleum CompanyThe use of gallium and indium salts for the immobilization of proteins
US4954354 *Jun 10, 1988Sep 4, 1990Phillips Petroleum CompanyProcess utilizing alcohol oxidase
US5283034 *Mar 26, 1992Feb 1, 1994Applied Immune Sciences, Inc.Stabilization of sterilized surfaces for research and medical use
US5730933 *Apr 16, 1996Mar 24, 1998Depuy Orthopaedics, Inc.Radiation sterilization of biologically active compounds
US6143508 *Jun 7, 1995Nov 7, 2000Rhone-Poulenc Rorer Pharmaceuticals Inc.Contacting mixture of cells with solid support having high density of specific receptor sites, whereby cells having complementary ligand become bound to surface and may be released from receptors
US6432653Aug 17, 1994Aug 13, 2002Aventis Pharmaceuticals Inc.Separation of cells from lymphs or myeloid linage with bonding and contacting cells
US8440875 *May 18, 2012May 14, 2013Uop LlcMethod and apparatus for high acid content feed for making diesel and aviation fuel
US20110217417 *May 4, 2009Sep 8, 2011Daniel PerlmanPhenolic antioxidant-supplemented infusion beverage
EP0345812A2 *Jun 9, 1989Dec 13, 1989Phillips Petroleum CompanyProcess utilizing alcohol oxidase
WO2003028488A1 *Aug 27, 2002Apr 10, 2003Brandsch RainerOxygen-absorbing agent in the form of a pourable granulate
WO2005085385A1 *Mar 2, 2005Sep 15, 2005Dominicis Mattia DeEnzymes as corrosion inhibitors by removal of oxygen dissolved in water
Classifications
U.S. Classification435/174, 426/654, 426/541, 426/10
International ClassificationA23L3/3571, A23L3/3463, B65D81/18, A23L3/34, A23L3/3436
Cooperative ClassificationB65D81/18, A23L3/3571, A23L3/3436
European ClassificationA23L3/3436, B65D81/18, A23L3/3571