Classifications

• • C—CHEMISTRY; METALLURGY
  • C13—SUGAR INDUSTRY
  • C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
  • C13B35/00—Extraction of sucrose from molasses
  • C13B35/02—Extraction of sucrose from molasses by chemical means
  • C13B35/04—Extraction of sucrose from molasses by chemical means by precipitation as alkaline earth metal saccharates
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
  • C07C51/42—Separation; Purification; Stabilisation; Use of additives
  • C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
  • C09F1/00—Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins
  • C09F1/04—Chemical modification, e.g. esterification
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
  • C10G29/20—Organic compounds not containing metal atoms
  • C10G29/22—Organic compounds not containing metal atoms containing oxygen as the only hetero atom
  • C10G29/24—Aldehydes or ketones
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G73/00—Recovery or refining of mineral waxes, e.g. montan wax
  • C10G73/42—Refining of petroleum waxes
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
  • C11B11/00—Recovery or refining of other fatty substances, e.g. lanolin or waxes
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
  • C11B11/00—Recovery or refining of other fatty substances, e.g. lanolin or waxes
  • C11B11/005—Lanolin; Woolfat
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
  • C11B3/00—Refining fats or fatty oils
  • C11B3/02—Refining fats or fatty oils by chemical reaction
  • C11B3/08—Refining fats or fatty oils by chemical reaction with oxidising agents
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
  • C11C1/00—Preparation of fatty acids from fats, fatty oils, or waxes; Refining the fatty acids
  • C11C1/08—Refining
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D13/00—Making of soap or soap solutions in general; Apparatus therefor
  • C11D13/02—Boiling soap; Refining
  • C11D13/06—Bleaching of soap or soap solutions
• • C—CHEMISTRY; METALLURGY
  • C13—SUGAR INDUSTRY
  • C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
  • C13B20/00—Purification of sugar juices
  • C13B20/08—Purification of sugar juices by oxidation or reduction
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
  • D06L4/13—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen using inorganic agents
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/20—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen
  • D06L4/21—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen combined with specific additives
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/20—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen
  • D06L4/22—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents
  • D06L4/24—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents using chlorites or chlorine dioxide
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/20—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen
  • D06L4/22—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents
  • D06L4/24—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents using chlorites or chlorine dioxide
  • D06L4/26—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which contain halogen using inorganic agents using chlorites or chlorine dioxide combined with specific additives
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/70—Multi-step processes

Definitions

• This invention relates to an improved process for effecting color improvement or bleaching of non-cellulosic organic materials.
• the invention is applicable to the treatment of a wide variety of such materials including the following: Carbohydrates such as sugar and starch; synthetics such as acetate rayon and nylon; sponges; walnut shells; resins such as shellac; oils, fats, waxes, soaps-and the like and fatty acids, such as oleic acid or red oil.
• the material to be bleached is subjected hyde in the presence of water.
• the material being treated is admixed with the chlorite and aldehyde in aqueous solution, the pH of the solution during the bleaching operation generally being maintained at not less than aboutfl.
• the function of the aldehyde in my improved bleaching process appears to be that of activating the chlorite rather than a direct action upon the organic material itself.
• the chlorites, or reaction products thereof are enabled to efiect the bleaching of the organic mato simultaneous action of a chlorite and an aldeterial either in an alkaline or substantially neutral environment.
• Chlorites useful in my process are those sufficiently soluble in water to provide an adequate concentration to efl'ect the desired bleaching. When the bleaching requirement is relatively low, less soluble chlorites may be used. However, for most purposes, I prefer the chlorites of the alkali and alkaline earth metals, such as sodium chlorite, NaClOz, and calcium chlorite, Ca(C1O2)2.
• aldehydes may be used, including the aliphatic aldehydes, aromatic aldehydes, other carbocyclic aldehydes and heterocyclic aldehydes.
• formaldehyde, acetaldehyde, paraformaldehyde, furfural, benzaldehyde, and 5 and 6 carbon atom aldose sugars and inverted sugars are particularly useful. All of these compounds are characterized by the CH0 group. In addition to those highly soluble in water, the relatively insoluble aldehydes have been found to function satisfactorily in most instances.
• Temperatures and concentrations are not usually critical and may be varied over a wide range. Increasing the temperature has generally been found to increase the rate of bleaching. Also, the ratio of chlorite to aldehyde may be widely varied. However, a molar ratio of chlorite to aldehyde of about 1:1 has been found generally useful.
• the temperature best suited for a particular operation will, to a considerable extent, depend upon the nature of the material being treated. Ordinary room temperature may frequently be employed with advantage but higher temperatures are usually desirable when treating a material normally solid where it is desired to effect the melting or solution thereof. Temperatures at which the material being treated becomes unstable or at which the material is deleteriously affected are to be avoided.
• Alkali metal phosphates such as the monosodium and disodium orthophosphates have been found to be particularly advantageous buffers for the purpose of the present invention, though other builers may be used with advantage. I have found that in the presence of such phosphates the consumption of chlorite in the bleaching operation is materially reduced, In some instances a saving of 50% of chlorite has been effected by the use of these phosphates, in conjunction with the other constituents of my bleaching solution previously noted.
• my invention is particularly useful in the treatment of either natural or synthetic materials of this type, including unsaponifiable petroleum waxes and saponiilable oils and waxes such as beeswax, carnauba wax, candelilla wax, corn oil and soya bean oil. It is especially applicable to the bleaching of soaps and similar alkaline reacting materials.
• such sponges may be bleached to an exceptionally high degree with no substantial tendering or weakening of their fiber structure so that their normal resistance to tearing apart in use is not substantially impaired.
• the bleaching of starch in accordance with my present invention, is with advantage enacted by subjecting the starch to the action of the chlorite and the aldehyde while in aqueous suspension.
• the bleaching of sugar, oils, fats, waxes, soaps, shellac, fatty acid and the like is with advantage effected by treating the material while in a liquid condition, 1. e., either molten or in aqueous solution, depending upon the characteristics of the particular material being treated.
• such materials either molten or in aqueous solution, may be admixed with a chlorite in the presence of water and the aidehyde thereafter added or the material to be treated may be admixed with the aldehyde in the presence of water and the chlorite added to this mixture.
• the resultant mixture is maintained at a temperature usually ranging from room temperature to about C., for a period of time sumcient to effect the desired bleaching and is thereafter cooled and separated.
• the soap may be melted by heating in water, the soap solution admixed with an aqueous chlorite solution and the desired amount of aldehyde thereafter added gradually or as a series of small proportions during agitation.
• the material In the treatment of wax or the like, which is solid at normal temperatures, the material is with advantage melted and an aqueous solution of the chlorite and the aldehyde admixed therewith or the chlorite and aldehyde may be separately added.
• Example I An aqueous solution was prepared by admixing 50 c. c. of pH 7 sodium phosphate buffer solution, 50 c. c. of an aqueous sodium chlorite solution containing 10 grams of available chlorine and 100 c. c. of a dilute aqueous formalin solution containing 2.2 grams of HCHO. 100 grams of soy-bean oil was then admixed with the resultant solution and allowed to stand for 2 hours, at the end of which time much of the original yellow color of the oil had been removed and, upon separation from the solution, a superior product was obtained. During the admixing of the oil with the solution and during the following 2 hour period a pH of about 7 and a temperature of about 25 C. were maintained.
• Example [I Beeswax was not only bleached but the texture thereof was made smoother by the following treatment: To 50 grams of beeswax melted in a water bath there was added 50 c. c. of an aqueous pH 7 sodium phosphate buffer solution, 100 c. c. of an aqueous sodium chlorite solution-containing 5 grams of available chlorine as chlorite and 1.9 c. c. of furfural. After admixing the solution and the melted beeswax, the admixture was permitted to stand for 1 hour at a temperature of 60 C. Thereafter, the wax was separated and allowed to solidify. The resultant product was found to have a much lighter 0010 than the original wax.
• Example III Cocoabutter was saponified by treatment with caustic soda and 200 grams of the resulting soap was melted with 200 grams of water. 1 gram of sodium chlorite dissolved in an equal weight of water was then added and admixed with the soap solution. This was followed by the addition of c. c. of aqueous formaldehyde solution prepared by dissolving 0.53 gram of 36% formalin in 100 c. c. of water. The addition of 10 ct, c. of
• this aqueous formaldehyde solution was repeated at 10 minute intervals until a total of 100 c. c. of the solution had been added. During this, period, the pH of the solution was approximately 9.3, no buffer being used, and the mixture was kept hot (about 100 C.) by the passage of steam therethrough. Thereafter, the bleached soap was cooled and separated. Its color was very white.
• Example IV A still further batch of cocoabutter soap was bleached, as described in Example III, except that the 10 c. 0. portions of the formaldehyde solutions were added at minute intervals. Re-
• Example VI 200 grams of yellow laundry soap was melted with an equal weight of water containing 0.48 gram of 36% formalin. At 15 minute intervals, 10 c. c. portions of an aqueous solution 'of commercial sodiiun chlorite, each containing 0.1 gram of chlorite, were added until a total of 100 c. c. of the chlorite'solution had been added. During this period, the pH of the solution was about 9.3, no buffer being used. A temperature of about 100 C. was maintained during this period, and thereafter until all of the available chlorite had disappeared, by the passage of steam through the,solution. Thereafter the soap was salted out and was found to be of a very good white color.
• Example VII For the purpose of illustrating the advantages derived from the use of the aldehyde in my and a still further bleaching of the soap obtained, During these tests, the pH of the soap solution was about 9.3. no buil'er being used.
• Example VIII A 25 gram piece of acetate rayon fabric was immersed in an aqueous .solution prepared by process, results of'the following experiments are presented To 500 grams of the yellow laundry soap of used in this operation.
• Example IX To 50 parts of crude brown sugar dissolved in 100 parts of water there was added 20 parts of a solution of sodium chlorite containing 1 part of available chlorine and 0.78 part of a formaldehyde solution containing 0.22 part of CHzO. The mixture was buffered at pH '7 by the presence of a phosphate bufier and was held at 40 0., for 1 hour. At the end of this period the solution was.
• Example X 118 parts of dark, reddish-brown shellac was dissolved in 11.8 parts of soda ash and 1000 part of water. To 100 parts of this solution there was added 1 part of available chlorine as sodium chlorite in 20 parts of aqueous solution and 0.78 part of a formaldehyde solution containing 0.22 part of 'CHzO. The solution was maintained at a temperature of 40 C. for one hour. No buffer was used and the pH of the solution was between '7 and 8.2. By the end of this period of treatment, the original dark purple colored solution had been bleached to-a light tan.
• Example XI A small reddish-brown sponge was immersed for 1 hour in 200 parts of an aqueous solution containing 1 part of available chlorine as sodium chlorite and 0.22 part of CHzO. During this period the solution was held at a temperature of 50 0., and at a pH of 6.6 by the use of a buffer. Thereafter the sponge was removed from the bleaching solution, washed and dried and was found to be of a light bufi' color.
• Example XII To 25 parts of crude corn starch of a greenish tint suspended inwater, there was added 1 part of available chlorine a sodium chlorite dissolved in 20 parts of aqueous solution and 0.22 part of CHzO in 20 parts of aqueous solution, the entire aqueous mixture amounting to 200 parts by weight. This suspension was held at a temperature of 50 C., for 1 hour. At the beginning of this period the pH of the solution was 7 and at the eiid thereof the pH had dropped to about 6.5. The starch was then filtered, washed and dried and was found to be of a pure white color free from any objectionable tints.
• Example XIII T0 50'- parts of red oil (oleic acid), heated in aboiling water bathto a temperature of about 100 and agitated by the passage of steam therethrough, there was added 0.5 part of available chlorine as sodium chlorite dissolved in parts of water. A solution of 0.25 part of 36% formalin in 10 parts of water was prepared and 1 part of this solution was added at 5 minute intervals until the total had been added. A few minutes after the final addition, all available chlorine had reacted. The fatty acid was then separated and was found to be a well bleached prodnot.
• the improvement which comprises subjecting the material to be bleached to the action of a substantially non-acidic aqueous solution of a chlorite of a metal of the group consisting of the alkali and alkaline earth metals in the presence of an aldehyde.
• the improvement which comprises subjecting the material to be bleached to the action of an aqueous solution having a pH not less than about 7 and containing a chlorite of a metal of the group consisting of the alkali and alkaline earth metals and an aldehyde.
• the improvement which comprises admixing the material to be bleached with a chlorite of a metal of the group consisting of the alkali and alkaline earth metals in the presence of water and an aldehyde at a pH not less than about '7.
• the improvement which comprises admixing the material to be bleached with a chlorite of a metal of the group consisting of the alkali and alkaline earth metals in the presence of water and an aldehyde and maintaining the hydrogen. ion concentration of the mixture at a pH not less than about '7 by the presence of an alkali metal phosphate buffer,
• the improvement which comprises subjecting the material to be bleached to the action of an aqueous solution having a pH not less than 8 about 7 and containing a chlorite of a metal of the group consisting of the alkali and alkaline earth metals and an aldehyde.
• the improvement which comprises subjecting the material to be bleached to the action of an aqueous solution having a pH not less than about 7 and containing a chlorite of a metal 01' the group consisting of the alkali and alkaline earth metals and an aldehyde.
• the improvement which comprises subjecting the starch to the action of a substantially non-acidic aqueous solution of a chlorite of a metal of the group consisting of the alkali and alkaline earth metals and an aldehyde.
• the improvement which comprises subjecting the sugar to the action of a substantially non-acidic aqueous solution of a chlorite of a metal of the group consisting of the alkali and alkaline earth metals and an aldehyde.
• the improvement which comprises subjecting the sugar to the action of an aqueous solution having a pH of about 7 and containing a chlorite of a metal of the group consisting of the alkali and alkaline earth metals and an aldehyde at a temperature of about 40 C. for a period of about 1 hour.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Chemical & Material Sciences (AREA)
• Wood Science & Technology (AREA)
• Textile Engineering (AREA)
• Inorganic Chemistry (AREA)
• Microbiology (AREA)
• Biochemistry (AREA)
• Detergent Compositions (AREA)
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• 0
  • BE BE465974D patent/BE465974A/xx unknown
• 1943
  • 1943-01-11 US US472052A patent/US2430674A/en not_active Expired - Lifetime
• 1944
  • 1944-01-31 GB GB1796/44A patent/GB576909A/en not_active Expired
  • 1944-02-01 GB GB1872/44A patent/GB576910A/en not_active Expired
• 1946
  • 1946-06-11 FR FR928932D patent/FR928932A/fr not_active Expired
• 1950
  • 1950-09-26 DE DES19567A patent/DE833943C/de not_active Expired
  • 1950-09-30 DE DES19908A patent/DE943105C/de not_active Expired

Patent Citations (5)

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