US1548864A - Manufacture of viscose films, etc. - Google Patents

Manufacture of viscose films, etc. Download PDF

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US1548864A
US1548864A US646478A US64647823A US1548864A US 1548864 A US1548864 A US 1548864A US 646478 A US646478 A US 646478A US 64647823 A US64647823 A US 64647823A US 1548864 A US1548864 A US 1548864A
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bath
film
cellulose
solution
viscose
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Brandenberger Jaques Edwin
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D10/00Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
    • D01D10/04Supporting filaments or the like during their treatment
    • D01D10/0436Supporting filaments or the like during their treatment while in continuous movement

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  • viscose cellulose strips, films, and the like derived from aqueous solutions of sodium cellulose xanthate generally termed viscose.
  • the xanthate solution was subjected to the coagulating action of a bath composed of an aqueous solution of ammonium sulphate or of other salts endowed with coaguating properties.
  • the film so obtained was then treated by means of various successive baths for the purpose, first, of purifying it by means of an aqueous solution of sodium chloride, then'of causing the xanthate to be transformed into cellulose under the action of a mineral acid, and lastly of washing it first with cold and next with hot Water.
  • the present invention consists of a new process for manufacturing in a continuous manner threads, filaments, strips, films, tubes, etc., starting from viscose. Its essential difference from the one hitherto used-.mention of which is to be found.
  • the viscose or solution ofsodium cellulose xanthate as it issues from the slotted extruding hopper passes into asuitable coagulating bath.
  • the lm so formed thentravels, in'a continuous manner,through a series of vats wherein it is supported by'suitable guide rollers, the successive vats containing baths.v adapted for subsequent operations.
  • the film On issuing from the first or coagulating bath, the film passes through a converting bath which causes the cellulose xanthate to be converted to cellulose; next the lm is subjected either to cold or to hot water 'Washing and then to the action of a desulphuring bath; thereafter, the film is subjected to a second washin in either hot or cold water, at any rate lot at first, and finally is subjected to the action of either a bleaching or a dyeing bath. After this last operation, the film is successively washed in running water, squeezed, put through a glycerine bath and ultimately dried either immediately or later.
  • Vat l: 00aguZatz ⁇ 0n.-Coagulation of the sodium cellulose xanthate is effected, as in former processes, by means of a bath containing, for instance, an aqueous solution-of sulphate of ammonia; I can also utilize aqueous solutions containing either a mixture ofsulphate of ammonia and an acid, or a mixture of sulphate of ammoniaI and a base, or bisulphate of soda or sulphate of soda with an acid added thereto, or magnesium sulphate or zinc sulphate; furthermore I may utilize any two normal sulphates in combination.A
  • composition (proportion-of constituents) of the coagulating bath actually used is determined by a number of factors, viz, the temperature of this bath, the degree to which the viscose has matured or ripened, the composition of .the viscose, the thickness Iof the film desired and the duration of contact of the vviscose with the coagulating solution, which is determined by length of travel in the bath and machine speed.
  • Vats 2 and 3 transforming bath.-This bath, which is designed to effect the transformation of the Xanthate into cellulose and which is utilized immediately after coagulation and previous to all other operations, consists of an aqueous solution of a mineral acid such as, for instance, hydrochloric acid, sulphuric acid etc.
  • a mineral acid such as, for instance, hydrochloric acid, sulphuric acid etc.
  • composition of this bath depends on the same factors as those already mentioned. There may be used, for instance, under the aforestated conditions, a solution of about 0.4 ⁇ gram or 0.5 gram.v of causticsodafor about ,100 cubic centimeters rof Waffel', and the film may be allowed l5, secondscontact withthebath. l .l I
  • Vats 7 and 8:washz'7igf-After desulphuration the film is subjected to awashingwith water in two vats. This washin isprefetabl effected hot, Aat anyrate ini e first vat, an at as high temperature as possible, even up to 100O C.
  • the desulphuring agent which is carried over with the film is in fact of an alkaline nature and thereforevery difficult to remove with cold water.
  • the hot washing may, if desired,'be followed by a cold water washing.
  • One method consists in treatingthe film in the first step by means Awof a bath composed of an aqueous solution of sodium hypochlorite, or of hypochlorite of lime containing a proportion of available chlorine amounting to from about 0.4 gram to 0.8 gram per l100 cubic centimeters, and then by means of a second bath (vat ll) composed of an aqueous solution of a mineral acid such as hydrochloricor sulphuric acid, for instance; in
  • vat 9 directly to vat 11 without entering vat l0 which becomes useless.
  • Another method involves the following: The film is subjected successively to the action of a bath composed of a solution of sodium hypochloritein vat 9, to a very brief cold water washing invat l0 and to the action of a mineral acid in vat 11. i
  • Still another operating method which may be used consists in treating the film with a solution of chlorine in water, the maximum concentration of which should be about 0.3 gram of chlorine in 100 cubic centimeters of Water. Part of the dissolved chlorine becomes transformed under the action of water into hydrochloric acid which imparts to the bath the required acidity.
  • Vat 14 gZg/cem'm baila-After washing, the film is subjected to a squeezing action between two smooth presser rollers, and is then treated in a glycerine bath.
  • the purpose of this treatment is to im art the required pliancy to the cellulose lm.
  • the film has al length of time of immersion in the glycerine bath of about eight seconds, and the concentration of the glycerine bath is determined by the use for which the film is intended. This concentration is greater when it is intended to make a more pliable flm,'and less when it is intended to make a less pliable film, but ordinarily the concentration is maintained so that the specific gravity of the glycerine solution is between 1.009 and 1.012.
  • the film may be squeezed and then placed in a suitable drying apparatus to dry.
  • the above described bleaching step may, of course, be replaced by a suitable dyein treatment, without the other operations eing modified in any Way.
  • the dyeing baths should have the same composition as those used for dyeing cotton, artificial silk or any other cellulosic fiber, in so-called continuous dyeing apparatus, the colors usually used for this purpose being the so-called direct colors.
  • Dyelng may also be effected at the same time as desulphurization by adding to the desulphuring bath coloring materials such as the so-called sulphur colors. It is also to be clearly understood that viscose may be used Which has been colored previous to coagulation either by means of sulphur colors or of any other coloring materials that will 4dissolve in viscose Without decomposing.
  • a process for the continuous manufacture of cellulose films and the like comprising the steps of coagulating an equeous solution of sodium cellulose Xanthate; passing the coagulated product through a transforming bath consisting of an aqueous solution of sulphuric acid containing about 4.5 grams of sulphuric acid per 100 cubic centimeters of water, and allowing the product to remain about 35 seconds in such bath; desulphuring the transformed product; and then bleaching, glycerinating and drying the same.
  • a process for'the continuous manufacture of cellulose films and the like comprising the steps of coagulating an aqueous solution. of sodium cellulose Xanthate; passing lution of sodium cellulose xanthate; passing the coagulated product through an aqueous l mineral acid solution to transform it into cellulose; Washing the transformed product with an aqueous solution of caustic soda containin about 0.5 gram of caustic soda per 100 cu ic centimeters of Water to desulphur it, and maintaining said product in such 'solution for about 15 seconds; and then bleaching, glycerinating and drying the desulphured product.
  • a process for the continuous manufacture of cellulose films and the like comprising the steps of coagulating an aqueous solution of sodium cellulose Xanthate by introducing it into an aqueous mixture of sodium sulphate and sulphurie acid; transforming the coagulated product into cellulose by passing 1t through an aqueous sulphurie acid solution; Washing the transformed product with caustic soda to desulphur it; then bleach- ⁇ ing the product by treating it first with an aqueous solution of sodium hypochlorite and then with an aqueous mineral acid solution; washing the bleached product with running Water; and then glycerinating and the same.
  • process for the continuous manufacture of cellulose films and the like comprising the steps of coagulating an aqueous solution of sodium cellulose Xanthate by introducing it into an aqueous mixture of sodium sulphate and sulphuric acid; transforming the coagulated product into cellulose by passing it throu h an aqueous sulphuric acid solution; was ing the transformed product with caustic soda to desulphur it; then bleaching the product by treating it first with an a ueous solution of sodium hypochlorite an then with an aqueous mineral acid solution, with a short Washing between the two treatments; washing the bleached product with running water; and then glycerinating and drying the same.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Textile Engineering (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Artificial Filaments (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Description

Aug. 11, 1925. 1,548,864
J. E. BRANDENBERGER MANUFACTURE 0F VISCOSE FILMS, ETC
Filed June 19 1925 Snow/bo@ Patentgd Aug. e11,' 1925. i
PATENT OFFICE.
JAQUEs EDWIN BRANDENBERGER, or NEuILL-stm-SEINE, FRANCE.
MANFACTURE F VISCOSE FILMS, ETC.
Application med June 19, 1923. serial No. 646,478.
To all 'whom t may concern.'
Be it known that I, TAQU'ES EDWIN BRAN- DENBERGE'R, a citizen ofSwitzerland, residing at Neuilly-sur-Seine, France, have in- `vented certain new and useful `Improvements in the Manufacture of Viscose Films, Etc., of which the following is a specifical tion.
manner, cellulose strips, films, and the like derived from aqueous solutions of sodium cellulose xanthate generally termed viscose. A
The expression in a continuous manner,
is intended to indicate that the operation isl conducted in such a way that the liquid viscose, running uninterruptedly into a coagulatin'g bath, 1s transformed without any interruption into a finished product: strips, films, etc., consisting of regenerated cellulose obtained from sodium cellulose xanthate.
lin certain former processes of maling film, the xanthate solution was subjected to the coagulating action of a bath composed of an aqueous solution of ammonium sulphate or of other salts endowed with coaguating properties. The film so obtained was then treated by means of various successive baths for the purpose, first, of purifying it by means of an aqueous solution of sodium chloride, then'of causing the xanthate to be transformed into cellulose under the action of a mineral acid, and lastly of washing it first with cold and next with hot Water.
The present invention consists of a new process for manufacturing in a continuous manner threads, filaments, strips, films, tubes, etc., starting from viscose. Its essential difference from the one hitherto used-.mention of which is to be found.
above-lies in this; 'that after the sodium cellulose xanthate has been coagulated in the first bath, its transformation into cellu- .a slotted hopper and allowing it to pass `etc., it would be necessary tov use instead of ythe slotted hopper, a suitable device containing apertures through which the Viscose is extruded, which apertures are adapted to make the kind of product desired.
In manufacturing film the viscose or solution ofsodium cellulose xanthate as it issues from the slotted extruding hopper passes into asuitable coagulating bath. The lm so formed thentravels, in'a continuous manner,through a series of vats wherein it is supported by'suitable guide rollers, the successive vats containing baths.v adapted for subsequent operations.
There is no occasion to emphasize the mechanicalfeatures ofthe ap aratus; and as regards the progress of the film through the various vats, the drawing which has been appended hereto is merely intended to indicate the sequence of baths and thus facilitate an understanding of the description, the actual invention-being primarily limited to the process.
On issuing from the first or coagulating bath, the film passes through a converting bath which causes the cellulose xanthate to be converted to cellulose; next the lm is subjected either to cold or to hot water 'Washing and then to the action of a desulphuring bath; thereafter, the film is subjected to a second washin in either hot or cold water, at any rate lot at first, and finally is subjected to the action of either a bleaching or a dyeing bath. After this last operation, the film is successively washed in running water, squeezed, put through a glycerine bath and ultimately dried either immediately or later.
Reference will again be made to each one of the various aforementioned operations, specifying the operating method and the characteristics for and of every one of them; the accompanying drawing showing diagrammatically the complete process as carried out in the successive vats which are indicated by reference numerals in regular order.
Vat l: 00aguZatz`0n.-Coagulation of the sodium cellulose xanthate is effected, as in former processes, by means of a bath containing, for instance, an aqueous solution-of sulphate of ammonia; I can also utilize aqueous solutions containing either a mixture ofsulphate of ammonia and an acid, or a mixture of sulphate of ammoniaI and a base, or bisulphate of soda or sulphate of soda with an acid added thereto, or magnesium sulphate or zinc sulphate; furthermore I may utilize any two normal sulphates in combination.A
When I use an acid coagulating bath or a bath containing bisulphates, I find that in this coagulating bath the xanthate immediately becomes partly transformed into cellulose.
The composition (proportion-of constituents) of the coagulating bath actually used is determined by a number of factors, viz, the temperature of this bath, the degree to which the viscose has matured or ripened, the composition of .the viscose, the thickness Iof the film desired and the duration of contact of the vviscose with the coagulating solution, which is determined by length of travel in the bath and machine speed.
There are, for instance, certain working conditions which hold ood for all the following explanations an to which the example given will refer. y
I will assume that the working speed is 25 meters per minute, and that the film to be obtained is to weigh from 25 to 30 grams per square meter. l
Under these conditions, and utilizing in the first bath as a coagulating solution a mixture of sodium sulphate and sulphuric acid, the best results are obtained with the following roportions, viz 10 grams of sodium sulpiiate. and 10 grams of sulphuric acid er 100 cubic centimeters, the film remaining in the coagulating bath for about 35 seconds. y l
Vats 2 and 3: transforming bath.-This bath, which is designed to effect the transformation of the Xanthate into cellulose and which is utilized immediately after coagulation and previous to all other operations, consists of an aqueous solution of a mineral acid such as, for instance, hydrochloric acid, sulphuric acid etc.
Under the aforestated conditions (speed 25 meters per minute, film weight 25 to 30 grams per square meter) good results are obtained with a. bath containing about 41/2` grams of sulphuric acid in 100 cubic centimeters of water, with a contact-duration of bath consists either of a liot aqueous solution i of, sodium sulphide, .the temperature of which may be as high as100 C., or of a solution of caustic soda or of la'solutio'n of both or of any other body or ksubstance'endowed with desulphuring properties. i
The composition of this bath depends on the same factors as those already mentioned. There may be used, for instance, under the aforestated conditions, a solution of about 0.4` gram or 0.5 gram.v of causticsodafor about ,100 cubic centimeters rof Waffel', and the film may be allowed l5, secondscontact withthebath. l .l I
Vats 7 and 8:washz'7igf-After desulphuration, the film is subjected to awashingwith water in two vats. This washin isprefetabl effected hot, Aat anyrate ini e first vat, an at as high temperature as possible, even up to 100O C. The desulphuring agent which is carried over with the film is in fact of an alkaline nature and thereforevery difficult to remove with cold water. The hot washing may, if desired,'be followed by a cold water washing.
Vats 9, 10 and 1] bZeacLng.-This operation may be carried out in various ways. One method consists in treatingthe film in the first step by means Awof a bath composed of an aqueous solution of sodium hypochlorite, or of hypochlorite of lime containing a proportion of available chlorine amounting to from about 0.4 gram to 0.8 gram per l100 cubic centimeters, and then by means of a second bath (vat ll) composed of an aqueous solution of a mineral acid such as hydrochloricor sulphuric acid, for instance; in
this case, the film passes from vat 9 directly to vat 11 without entering vat l0 which becomes useless. Another method involves the following: The film is subjected successively to the action of a bath composed of a solution of sodium hypochloritein vat 9, to a very brief cold water washing invat l0 and to the action of a mineral acid in vat 11. i
Still another operating method which may be used consists in treating the film with a solution of chlorine in water, the maximum concentration of which should be about 0.3 gram of chlorine in 100 cubic centimeters of Water. Part of the dissolved chlorine becomes transformed under the action of water into hydrochloric acid which imparts to the bath the required acidity.
Vats `1.@ and 13." washing- After bleaching by means of any one of the above-described methods, the film is subjected to a washing in rapidly running water. This washing may be effected hot or cold, or even in two different baths, one hot and the other cold, with about 15 secondsv stay in each bath.
Vat 14: gZg/cem'm baila-After washing, the film is subjected to a squeezing action between two smooth presser rollers, and is then treated in a glycerine bath. The purpose of this treatment is to im art the required pliancy to the cellulose lm.
With the assumed speed of 25 meters per minute, the film has al length of time of immersion in the glycerine bath of about eight seconds, and the concentration of the glycerine bath is determined by the use for which the film is intended. This concentration is greater when it is intended to make a more pliable flm,'and less when it is intended to make a less pliable film, but ordinarily the concentration is maintained so that the specific gravity of the glycerine solution is between 1.009 and 1.012.
After this treatment, the film may be squeezed and then placed in a suitable drying apparatus to dry.
If a colored film is desired, the above described bleaching step may, of course, be replaced by a suitable dyein treatment, without the other operations eing modified in any Way. The dyeing baths should have the same composition as those used for dyeing cotton, artificial silk or any other cellulosic fiber, in so-called continuous dyeing apparatus, the colors usually used for this purpose being the so-called direct colors. Dyelng may also be effected at the same time as desulphurization by adding to the desulphuring bath coloring materials such as the so-called sulphur colors. It is also to be clearly understood that viscose may be used Which has been colored previous to coagulation either by means of sulphur colors or of any other coloring materials that will 4dissolve in viscose Without decomposing.
No claims are contained in the present case for the dyeing step, however, as'such claims form' the subject matter of a divisional application No. 708,316, filed April 22, 1924.
It is to be understood that the process applies equally to the case Where inert substances such as barium sulphate, kaolin, etc., have been introduced into the viscose.
I claim as my invention:
1. A process for the continuous manufacture of cellulose films and the like, comprising the steps of coagulating an equeous solution of sodium cellulose Xanthate; passing the coagulated product through a transforming bath consisting of an aqueous solution of sulphuric acid containing about 4.5 grams of sulphuric acid per 100 cubic centimeters of water, and allowing the product to remain about 35 seconds in such bath; desulphuring the transformed product; and then bleaching, glycerinating and drying the same.
riff
2. A process for'the continuous manufacture of cellulose films and the like, comprising the steps of coagulating an aqueous solution. of sodium cellulose Xanthate; passing lution of sodium cellulose xanthate; passing the coagulated product through an aqueous l mineral acid solution to transform it into cellulose; Washing the transformed product with an aqueous solution of caustic soda containin about 0.5 gram of caustic soda per 100 cu ic centimeters of Water to desulphur it, and maintaining said product in such 'solution for about 15 seconds; and then bleaching, glycerinating and drying the desulphured product.
4. A process for the continuous manufacture of cellulose films and the like, comprising the steps of coagulating an aqueous solution of sodium cellulose Xanthate by introducing it into an aqueous mixture of sodium sulphate and sulphurie acid; transforming the coagulated product into cellulose by passing 1t through an aqueous sulphurie acid solution; Washing the transformed product with caustic soda to desulphur it; then bleach- `ing the product by treating it first with an aqueous solution of sodium hypochlorite and then with an aqueous mineral acid solution; washing the bleached product with running Water; and then glycerinating and the same. process for the continuous manufacture of cellulose films and the like, comprising the steps of coagulating an aqueous solution of sodium cellulose Xanthate by introducing it into an aqueous mixture of sodium sulphate and sulphuric acid; transforming the coagulated product into cellulose by passing it throu h an aqueous sulphuric acid solution; was ing the transformed product with caustic soda to desulphur it; then bleaching the product by treating it first with an a ueous solution of sodium hypochlorite an then with an aqueous mineral acid solution, with a short Washing between the two treatments; washing the bleached product with running water; and then glycerinating and drying the same.
In testimony whereof I affix my signature.
JAQUES EDWIN BRANDENBERGER.
US646478A 1923-02-16 1923-06-19 Manufacture of viscose films, etc. Expired - Lifetime US1548864A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
FR573533D FR573533A (en) 1923-02-16 1923-02-16 Process for the continuous manufacture of film-strips, horsehair, threads, cellulose tubes starting from an aqueous solution of sodium cellulose xanthate, called viscose
US646478A US1548864A (en) 1923-02-16 1923-06-19 Manufacture of viscose films, etc.
GB32099/23A GB211446A (en) 1923-02-16 1923-12-29 Improved manufacture of cellulose films, threads, tubes or the like
US708316A US1601289A (en) 1923-02-16 1924-04-22 Manufacture of viscose films, etc.

Applications Claiming Priority (3)

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FR573533T 1923-02-16
US646478A US1548864A (en) 1923-02-16 1923-06-19 Manufacture of viscose films, etc.
US708316A US1601289A (en) 1923-02-16 1924-04-22 Manufacture of viscose films, etc.

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2460282A (en) * 1941-07-22 1949-02-01 Aerovox Corp Regenerated cellulose dielectric material and process of producing the same
US2494951A (en) * 1946-05-10 1950-01-17 Svenska Rayon Ab Process for manufacturing regenerated cellulose webs
US2862245A (en) * 1951-09-07 1958-12-02 American Viscose Corp Method for producing films
US3354141A (en) * 1964-02-06 1967-11-21 Kasser Ivan Michael Method for preparing viscose spinning solution
US3429771A (en) * 1964-02-06 1969-02-25 Alexander Kasser Cellulose dissolving pulp produced from grain parchment
US11597779B2 (en) 2017-12-04 2023-03-07 Nanollose Limited Methods for producing a viscose dope from microbial cellulose

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2454515A (en) * 1938-10-29 1948-11-23 Polaroid Corp Light-polarizing sheet of molecularly oriented transparent linear high polymer dyed with dichroic substance and process of manufacture
US2424904A (en) * 1940-10-05 1947-07-29 Ruben Samuel Process for the treatment of regenerated sheet cellulose to improve its dielectric properties
US3872196A (en) * 1972-12-04 1975-03-18 Tee Pak Inc Process for plasticizing and partially drying tubular film casings for edible products
AT2207U1 (en) * 1998-03-12 1998-06-25 Chemiefaser Lenzing Ag METHOD FOR PRODUCING CELLULOSIC MOLDED BODIES

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2460282A (en) * 1941-07-22 1949-02-01 Aerovox Corp Regenerated cellulose dielectric material and process of producing the same
US2494951A (en) * 1946-05-10 1950-01-17 Svenska Rayon Ab Process for manufacturing regenerated cellulose webs
US2862245A (en) * 1951-09-07 1958-12-02 American Viscose Corp Method for producing films
US3354141A (en) * 1964-02-06 1967-11-21 Kasser Ivan Michael Method for preparing viscose spinning solution
US3429771A (en) * 1964-02-06 1969-02-25 Alexander Kasser Cellulose dissolving pulp produced from grain parchment
US11597779B2 (en) 2017-12-04 2023-03-07 Nanollose Limited Methods for producing a viscose dope from microbial cellulose

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GB211446A (en) 1925-03-26
US1601289A (en) 1926-09-28
FR573533A (en) 1924-06-25

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