US2065188A - Manufacture of viscose - Google Patents
Manufacture of viscose Download PDFInfo
- Publication number
- US2065188A US2065188A US719969A US71996934A US2065188A US 2065188 A US2065188 A US 2065188A US 719969 A US719969 A US 719969A US 71996934 A US71996934 A US 71996934A US 2065188 A US2065188 A US 2065188A
- Authority
- US
- United States
- Prior art keywords
- cellulose
- alkali
- viscose
- per cent
- viscosity
- 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.)
- Expired - Lifetime
Links
- 229920000297 Rayon Polymers 0.000 title description 15
- 238000004519 manufacturing process Methods 0.000 title description 12
- 229920002678 cellulose Polymers 0.000 description 50
- 239000001913 cellulose Substances 0.000 description 47
- 235000010980 cellulose Nutrition 0.000 description 45
- 239000003513 alkali Substances 0.000 description 36
- 238000000034 method Methods 0.000 description 17
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 13
- 229910017604 nitric acid Inorganic materials 0.000 description 13
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 10
- 239000002023 wood Substances 0.000 description 10
- 229920002955 Art silk Polymers 0.000 description 9
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000003518 caustics Substances 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 230000029087 digestion Effects 0.000 description 7
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000012991 xanthate Substances 0.000 description 7
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000009987 spinning Methods 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- 238000005517 mercerization Methods 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 230000005070 ripening Effects 0.000 description 2
- 241000218631 Coniferophyta Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DBNPDRYVYQWGFW-UHFFFAOYSA-N N.[Cu]=O Chemical compound N.[Cu]=O DBNPDRYVYQWGFW-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000011346 highly viscous material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/06—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
- D01F2/08—Composition of the spinning solution or the bath
Definitions
- Our present invention relates to the manufacture of artificial articles such as artificial threads, sheets, ribbons from cellulose.
- One of its objects is to provide an improved process for the manufacture of artificial articles which is efficient and involves a considerable reduction of costs. Further objects will be seen from the detailed specification following hereafter.
- the process according to this invention does not start as usual from dried sheets of sulfite pulp, but from a highly viscous cellulose as obtained according to one of the known processes for disintegrating cellulose-containing materials by means of nitric acid and still contains water from its manufacture.
- this highly viscous material is converted into alkali-cellulose by the action of caustic alkali and the viscosity of the material is reduced, particularly by the action of an alkali sulfide and gases containing oxygen.
- the alkali-cellulose is mixed with carbon disulfide and dissolved so as to form viscose containing more than 5 per cent of cellulose; this viscose is spun in known 25 manner into artificial silk, sheets, ribbons and the like.
- the whole process from the digestion of the wood to the spinning of artificial silk is performed in a very short time and with the con sumption of very small quantities of chemicals.
- the cellulose digested by means of nitric acid is particularly suited for the manufac- 10 ture of solid and purelywhite artificial silk.
- the high viscosities may be reduced Without difficulty within a short time and indeed with avoidance of tedious intermediate operations, such as dipping, ripening, etc. 15
- an alkali sulfide is used the effect of which, as has been found, is enhanced to an extent hitherto unknown, by the infiuence of a gas containing oxygen, for instance air. This operation is accompanied by a strong development of heat.
- an alkali sulfide there may also be employed a polysulfide or any other substance having the same effect.
- the treatment with air of the alkali cellulose containing alkali sulfide is preferably performed directly after centrifuging the alkali cellulose or draining it.
- the alkali-cellulose may also be treated with air containing hydrogen sulfide, the formation of the sodium sulfide and the action of this substance on the alkali cellulose in the presence of air occurring simultaneously or in succession.
- the proportion of the alkali sulfide is adjusted to that required for the desired reduction of viscosity. In the finished alkali cellulose the alkali sulfide added should be consumed practically completely.
- the treatment of the alkali-cellulose containing an alkali sulfide may be performed if required also while reducing the alkali-cellulose to fibres or also when comminuting the material in the xanthogenating machine prior to the treatment with carbon bisulfide.
- Highly viscous celluloses according to the invention are such as have a copper viscosity higher than 200".
- nitric acid By the process of digesting with nitric acid, however, there may be obtained celluloses having a copper viscosity of 1000".
- These celluloses, too, may be utilized for the manufacture in a. continuous operation of spinning solutions having a low viscosity.
- the copper viscosity is determined, without the access of atmospheric oxygen, by measuring the time of flow of a copper oxide-ammonia solution containing 1 per cent of cellulose and accurately adjusted to 20 per cent of NH3 and 1.3 per cent of Cu. The time during which 50 cc.
- - of cellulose-copper oxide-ammonia solution flows at 20 0.
- the capillary orifice of a viscosimeter represents an exact measurement of the viscosity of the cellulosic material.
- the viscosimeter is standardized with water and so adjusted that a period of 10 seconds is required for the flow of the water.
- Conifer wood or deciduous wood is disintegrated with nitric acid according to one of the known processes.
- the non-cellulosic constituents rendered soluble by the nitric acid are then extracted by treatment with waste liquor containing alkali sulfide obtained in the mercerization of the preceding batch of cellulose, and the cellulose pulp thus obtained, after previous chlorination for extracting the last remnants of ligneous matter is bleached in the usual manner.
- the cellulose thus prepared has a copper viscosity of about 350 to 1000", according to the kind of wood employed and according to the digestion process adopted.
- the bleached material which by centrifuging and draining has been brought to a dry weight of 20 to 35% is treated with a caustic soda solution of such a strength that inclusive. of the moisture of the material the final concentration amounts to 12 to 18 per cent by volume of NaOH and 10 to 4 per cent by volume of NazS.
- The. amount of cellulose in the soaking liquor amounts to about 5 per cent by volume. After the mass has been stirred for 2 hours it is centrifuged for about 3 hours until it has three times the weight of the cellulose. During the centrifuging the viscosity due to the action of the atmospheric oxygen, is reduced to about 45", the temperature rising from 20 to 30 to 40 C.
- the alkali cellulose thus obtained is then comminuted for a short time in the kneader of a xanthating machine and sulfided in the same apparatus by means of 25 per cent by volume of carbon bisulfide added within 1 hours.
- the temperature is preferably not allowed to exceed 30 C.
- the finished cellulose xanthate is finally dissolved by means of a dilute caustic soda solution to form a viscose containing 7.5 per cent of cellulose and 6.5 per cent of alkali.
- the viscose obtained by this process is clearer than the ordinary viscose obtained from sulfite pulp, so that artificial threads with fine individual titers (indi vidual titer equal to 1 or lower) may easily be produced.
- the filtered viscose is spun in the usual manner into a bath at a temperature of 50 0., containing 13 per cent of sulfuric acid and 28 per cent of sodium sulfate.
- the artificial silk obtained after being desulfurized in the usual way is bright and of a pure White, without application of the usual bleaching operation with hypochlorite or baths containing hydrogen peroxide.
- the silk has a tensile strength of 150 to 160 gr. per 100 deniers, and an extensibility of 20 per cent.
- artificial silk may be obtained having a tensile strength of 200 and 300 gr. and more per 100 deniers.
- a process of manufacturing viscose which comprises subjecting wood to digestion with nitric acid, removing the soluble non-cellulosic substances by means of a solution of caustic alkali, washing the cellulose pulp, reducing the content of water of the pulp by mechanical means to to per cent, converting the wet cellulose into alkali cellulose by the addition of a solution of caustic alkali, subjecting the alkali cellulose to the action of an oxygen-containing gas and a viscosity-reducing material selected from the group consisting of alkali sulfides, hydrogen sulfide and alkali polysulfides, converting the alkali cellulose into cellulose xanthate and dissolving said xanthate to form a viscose solution.
- a process of manufacturing viscose which comprises subjecting wood to digestion with nitric acid, removing the soluble non-cellulosic sub stances by means of a solution of caustic alkali, washing the cellulose pulp, reducing the content of water of the pulp by mechanical means to 65 to 80 per cent, converting the wet cellulose into alkali cellulose by the addition of a solution'of caustic alkali, subjecting the alkali cellulose to the action of alkali sulfide and an oxygen-containing gas, converting the alkali cellulose into cellulose xanthate, and dissolving said xanthate to form a viscose solution.
- a process of manufacturing viscose which comprises subjecting wood to digestion with nitric acid, removing the soluble non -cellulosic substances by means of a solution of caustic alkali, washing the cellulose pulp reducing the content of water of the pulp by mechanical meansto 65 to 80 per cent, converting the wet cellulose into alkali cellulose by the addition of a solution of caustic alkali, subjecting the alkali cellulose to the action of alkali sulfide and oxygen-containing gas, converting the alkali cellulose into cellulose xanthate, and dissolving said xanthate to form a viscose solution.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Artificial Filaments (AREA)
Description
Patented Dec. 22, 1936 UNITED STATES PATENT OFFICE,
MANUFACTURE OF VISCOSE Main, Germany No Drawing. Application April 10, 1934, Serial No. 719,969. In Germany April 20, 1933 73 Claims. (01. 260-100) Our present invention relates to the manufacture of artificial articles such as artificial threads, sheets, ribbons from cellulose.
One of its objects is to provide an improved process for the manufacture of artificial articles which is efficient and involves a considerable reduction of costs. Further objects will be seen from the detailed specification following hereafter.
The process according to this invention does not start as usual from dried sheets of sulfite pulp, but from a highly viscous cellulose as obtained according to one of the known processes for disintegrating cellulose-containing materials by means of nitric acid and still contains water from its manufacture. According to the invention, this highly viscous material is converted into alkali-cellulose by the action of caustic alkali and the viscosity of the material is reduced, particularly by the action of an alkali sulfide and gases containing oxygen. The alkali-cellulose is mixed with carbon disulfide and dissolved so as to form viscose containing more than 5 per cent of cellulose; this viscose is spun in known 25 manner into artificial silk, sheets, ribbons and the like. The whole process from the digestion of the wood to the spinning of artificial silk is performed in a very short time and with the con sumption of very small quantities of chemicals.
30 If, for preserving the alpha-cellulose, wood is digested in known manner with small amounts of nitric acid or with nitrogen oxides and air, for instance according to U. S. patents Nos. 1,736,080 and 1,840,198, a cellulose is obtained which even 5 after it has been bleached in the usual way is still highly viscous and is very well suited as a starting material for the manufacture of artificial silk and yields a bright silk even when the alkalicellulose has not been ripened. Since'the diges- 40 tion by means of nitric acid dispenses with the application of pressure vessels, it may be carried through with advantage also when starting from smaller batches and therefore, it is the very process to be used in direct connection with the manu- 45 facture of artificial silk. In the process of digesting wood by using nitric acid the great difficulty, experienced in the sulfite process, namely removal of the waste liquors, exists in a much lower degree. It becomes possible, therefore, to
50 perform the digestion of wood even in those artificial silk factories which are not favorably situated for removal of waste liquors. Furthermore, the combination of the production of the pulp by the nitric acid process with the manufacture of 55 the artificial silk is of a great technical value for the reason that this digestion process requires considerable amounts of alkaline liquors for dissolving the non-cellulose constituents rendered soluble by the nitric acid and that alkaline liquors suitable for this purpose are obtained in large 5 quantities from the mercerization of the cellulose in making the viscose.
Due to its high viscosity and its high degree of whiteness the cellulose digested by means of nitric acid is particularly suited for the manufac- 10 ture of solid and purelywhite artificial silk. According to the invention the high viscosities may be reduced Without difficulty within a short time and indeed with avoidance of tedious intermediate operations, such as dipping, ripening, etc. 15 For reducing the viscosity of the pulp, an alkali sulfide is used the effect of which, as has been found, is enhanced to an extent hitherto unknown, by the infiuence of a gas containing oxygen, for instance air. This operation is accompanied by a strong development of heat. Instead of an alkali sulfide there may also be employed a polysulfide or any other substance having the same effect. The treatment with air of the alkali cellulose containing alkali sulfide is preferably performed directly after centrifuging the alkali cellulose or draining it. The alkali-cellulose may also be treated with air containing hydrogen sulfide, the formation of the sodium sulfide and the action of this substance on the alkali cellulose in the presence of air occurring simultaneously or in succession. The proportion of the alkali sulfide is adjusted to that required for the desired reduction of viscosity. In the finished alkali cellulose the alkali sulfide added should be consumed practically completely. By this mode of operation it is possible to reduce the viscosity of a cellulose having a copper viscosity, for instance, of 400 to within three hours. This is to be contrasted with the usual time necessary for the 40 ripening of the alkali cellulose, namely at least 6 days.
When in this process centrifuges or suction filters are used it is not necessary to specially comminute the alkali cellulose. Of course, the treatment of the alkali-cellulose containing an alkali sulfide may be performed if required also while reducing the alkali-cellulose to fibres or also when comminuting the material in the xanthogenating machine prior to the treatment with carbon bisulfide.
Highly viscous celluloses according to the invention are such as have a copper viscosity higher than 200". By the process of digesting with nitric acid, however, there may be obtained celluloses having a copper viscosity of 1000". These celluloses, too, may be utilized for the manufacture in a. continuous operation of spinning solutions having a low viscosity.
The copper viscosity is determined, without the access of atmospheric oxygen, by measuring the time of flow of a copper oxide-ammonia solution containing 1 per cent of cellulose and accurately adjusted to 20 per cent of NH3 and 1.3 per cent of Cu. The time during which 50 cc.
- of cellulose-copper oxide-ammonia solution flows at 20 0., through the capillary orifice of a viscosimeter represents an exact measurement of the viscosity of the cellulosic material. The viscosimeter is standardized with water and so adjusted that a period of 10 seconds is required for the flow of the water.
The following example illustrates the invention.
Conifer wood or deciduous wood is disintegrated with nitric acid according to one of the known processes. The non-cellulosic constituents rendered soluble by the nitric acid are then extracted by treatment with waste liquor containing alkali sulfide obtained in the mercerization of the preceding batch of cellulose, and the cellulose pulp thus obtained, after previous chlorination for extracting the last remnants of ligneous matter is bleached in the usual manner. The cellulose thus prepared has a copper viscosity of about 350 to 1000", according to the kind of wood employed and according to the digestion process adopted. The bleached material, which by centrifuging and draining has been brought to a dry weight of 20 to 35% is treated with a caustic soda solution of such a strength that inclusive. of the moisture of the material the final concentration amounts to 12 to 18 per cent by volume of NaOH and 10 to 4 per cent by volume of NazS. The. amount of cellulose in the soaking liquor amounts to about 5 per cent by volume. After the mass has been stirred for 2 hours it is centrifuged for about 3 hours until it has three times the weight of the cellulose. During the centrifuging the viscosity due to the action of the atmospheric oxygen, is reduced to about 45", the temperature rising from 20 to 30 to 40 C.
The alkali cellulose thus obtained is then comminuted for a short time in the kneader of a xanthating machine and sulfided in the same apparatus by means of 25 per cent by volume of carbon bisulfide added within 1 hours. The temperature is preferably not allowed to exceed 30 C. The finished cellulose xanthate is finally dissolved by means of a dilute caustic soda solution to form a viscose containing 7.5 per cent of cellulose and 6.5 per cent of alkali. The viscose obtained by this process is clearer than the ordinary viscose obtained from sulfite pulp, so that artificial threads with fine individual titers (indi vidual titer equal to 1 or lower) may easily be produced.
60 hours after dissolution the filtered viscose is spun in the usual manner into a bath at a temperature of 50 0., containing 13 per cent of sulfuric acid and 28 per cent of sodium sulfate.
The artificial silk obtained after being desulfurized in the usual way, is bright and of a pure White, without application of the usual bleaching operation with hypochlorite or baths containing hydrogen peroxide. The silk has a tensile strength of 150 to 160 gr. per 100 deniers, and an extensibility of 20 per cent. When varying the spinning conditions particularly when adopting spinning baths having a high concentration of acid, artificial silk may be obtained having a tensile strength of 200 and 300 gr. and more per 100 deniers.
What we claim is:
1. A process of manufacturing viscose which comprises subjecting wood to digestion with nitric acid, removing the soluble non-cellulosic substances by means of a solution of caustic alkali, washing the cellulose pulp, reducing the content of water of the pulp by mechanical means to to per cent, converting the wet cellulose into alkali cellulose by the addition of a solution of caustic alkali, subjecting the alkali cellulose to the action of an oxygen-containing gas and a viscosity-reducing material selected from the group consisting of alkali sulfides, hydrogen sulfide and alkali polysulfides, converting the alkali cellulose into cellulose xanthate and dissolving said xanthate to form a viscose solution.
2. A process of manufacturing viscose which comprises subjecting wood to digestion with nitric acid, removing the soluble non-cellulosic sub stances by means of a solution of caustic alkali, washing the cellulose pulp, reducing the content of water of the pulp by mechanical means to 65 to 80 per cent, converting the wet cellulose into alkali cellulose by the addition of a solution'of caustic alkali, subjecting the alkali cellulose to the action of alkali sulfide and an oxygen-containing gas, converting the alkali cellulose into cellulose xanthate, and dissolving said xanthate to form a viscose solution.
3. A process of manufacturing viscose which comprises subjecting wood to digestion with nitric acid, removing the soluble non -cellulosic substances by means of a solution of caustic alkali, washing the cellulose pulp reducing the content of water of the pulp by mechanical meansto 65 to 80 per cent, converting the wet cellulose into alkali cellulose by the addition of a solution of caustic alkali, subjecting the alkali cellulose to the action of alkali sulfide and oxygen-containing gas, converting the alkali cellulose into cellulose xanthate, and dissolving said xanthate to form a viscose solution.
KARL K'o'ssLINGER.
ALFONS BAYERL.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE434547X | 1933-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2065188A true US2065188A (en) | 1936-12-22 |
Family
ID=6506637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US719969A Expired - Lifetime US2065188A (en) | 1933-04-20 | 1934-04-10 | Manufacture of viscose |
Country Status (5)
Country | Link |
---|---|
US (1) | US2065188A (en) |
BE (1) | BE434547A (en) |
FR (1) | FR772152A (en) |
GB (1) | GB434547A (en) |
NL (1) | NL37939C (en) |
-
0
- BE BE434547D patent/BE434547A/xx unknown
- NL NL37939D patent/NL37939C/xx active
-
1934
- 1934-04-10 US US719969A patent/US2065188A/en not_active Expired - Lifetime
- 1934-04-19 FR FR772152D patent/FR772152A/en not_active Expired
- 1934-04-20 GB GB11964/34A patent/GB434547A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR772152A (en) | 1934-10-24 |
NL37939C (en) | |
BE434547A (en) | |
GB434547A (en) | 1935-09-04 |
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