US2591242A - Process for the manufacture of yarns from hydroxylated polyvinyl compounds - Google Patents
Process for the manufacture of yarns from hydroxylated polyvinyl compounds Download PDFInfo
- Publication number
- US2591242A US2591242A US139458A US13945850A US2591242A US 2591242 A US2591242 A US 2591242A US 139458 A US139458 A US 139458A US 13945850 A US13945850 A US 13945850A US 2591242 A US2591242 A US 2591242A
- Authority
- US
- United States
- Prior art keywords
- yarn
- package
- spinning
- yarns
- solution
- 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
- 238000000034 method Methods 0.000 title claims description 10
- 238000004519 manufacturing process Methods 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 title description 5
- 229920002554 vinyl polymer Polymers 0.000 title description 5
- 239000000843 powder Substances 0.000 claims description 20
- 238000009987 spinning Methods 0.000 claims description 19
- 230000001464 adherent effect Effects 0.000 claims description 16
- 239000000243 solution Substances 0.000 claims description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 10
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- 238000004804 winding Methods 0.000 claims description 6
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 10
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 10
- 235000011130 ammonium sulphate Nutrition 0.000 description 10
- 239000001166 ammonium sulphate Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000007790 scraping Methods 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- GKQHIYSTBXDYNQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1 GKQHIYSTBXDYNQ-UHFFFAOYSA-M 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- -1 POLY- VINYL COMPOUNDS Chemical class 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Images
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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/14—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated alcohols, e.g. polyvinyl alcohol, or of their acetals or ketals
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S425/00—Plastic article or earthenware shaping or treating: apparatus
- Y10S425/017—Filament stretching apparatus
Description
April 1, 1952 N. DRISCH ETAL 2,591,242
PROCESS FOR THE MANUFACTURE OF YARNS FROM HYDROXYLATED POLYVINYL COMPOUNDS Filed Jan. 19, 1950 Patented Apr. 1, 195.2
UNITED STATES PATENT OFFICE rnoonss FOR THE MANUFACTURE OF YARNS FROM HYDROXYLATED POLY- VINYL COMPOUNDS Nicolas Drisch and Paul Herrbach, Paris, France, assigncrs, by mesne assignments, to Textile and Chemical Research Company Limited, St. Peter Port, Guernsey, Channel Islands, a corporation of Great Britain Application January 19, 1950, Serial No. 139,458 In France February 1, 1949 Claims.
1 This invention relates to the manufacture of spun yarn from hydroxylated polyvinyl compounds in an ammonium sulphate spinning bath The spinning of soluble rayon may be accom--,
plished with the aid of various hydrophilic substances such as sodium alginate, carboxymethyl cellulose, etc.
Filaments obtained from sodium alginate solutions are lacking in elongation. They will not dissolve in aqueous medium, but only in slightly alkaline medium. Alginate threads are generally based on the calcium salt of alginic acid.
Filamentsof the aluminum salt of celluloseglycolic acid are not readily soluble in weak alkaline medium, but require more strongly a1kaline media which may be harmful to the wool with which such products are often mixed.
The spinning of solutions of hydroxylated polyvinyl compounds is described in general in United States Patent No. 2,388,325. For example, aqueous solutions of polyvinyl alcohol are spun in a hot aqueous bath containing 35 per cent of ammonium sulphate. The filaments so obtained are stretched and collected in a spinning pot. The spinning is done with the usual equipment used for artificial textiles. The filaments obtained, impregnated with ammonium sulphate, are subjected to washing by a solution of 50 per cent acetone in water. This washing is tedious and difiioult because of the low solubility of ammonium sulphate in the solvent mixture. Before drying, the cakes are re-treated with pure acetone.
Among the disadvantages of this process are the need for an organicsolvent which must be recovered, the danger of explosion of the solvent air mixture, and the solvent lossep.
The present invention provides a simpler and more economical method of manufacturing yarn from hydroxylated poiyvinyl compounds, such as polyvinyl alcohol.
According to the invention, the cakes of yarn are dried in a ventilated hot air drier, producing a package of yarn carrying ammonium sulphate in the form of an impalpably line powder not affecting the strength of the individual filaments. The cake is re-wound by passing the yarn through a tensioning device set to introduce friction adapted to remove most of the ammonium sulphate powder coating the yarn. The yarn obtained is characterized by a very soft feel, complete independence of all filaments, and very satisfactory mechanical properties. The following example will afford a clearer understanding of the invention, but is of course in no way restrictive.
Eazample A solution of 15 per cent polyvinyl alcohol of low viscosity is prepared by heating with water. This solution is readily filterable, even after cooling and has a viscosity of about 115 poises at 20 C. It is desirable to add 1 per cent of lauryl pyridinium chloride calculated on the polyvinyl alcohol. The resulting solution is filtered and deaerated.
The spinning is effected in a known way. The solution is spun in an aqueous bath containing 35 per cent ammonium sulphate at C. from a spinneret having 30 holes of /100 mm. The thread is stretched 410 per cent between two rollers, the final speed being 40 to min. The feed of the solution is controlled so as to yield 5 d. filaments. The resulting yarn is collected in cakes in a spinning pot with a speed of 6000 R. P. M. The resulting cakes are dried at C. in a ventilated drier. They are unwound on ordinary spoolers, with the filament passing through a tensioning device set to produce tensions of the order of 1 gram per denier, e. g. in a grid tensioning device, to scrape ad the adhering saline powder.
In the drawing the figure is a diagrammatic representation of one type of apparatus in which this process can be carried out.
Referring to the drawing the cake it of yarn II is unwound through guides 12 and I3 onto a spool 14 which is driven by a drive roller 15. Interposed between the guides I2 and I3 is a grid tensioning and scraping device comprising sets of bars i6 and H which are interleaved and around which the yarn passes. The friction produced by the bars is controlled by varying the overlap of the two sets of bars. In operation the bars introduce sufiicient friction to scrape the ammonium sulphate powder from the yarn as above described.
The resulting yarn has a dry strength of 1.90 grams per denier with an elongation at break of 40 per cent, and contains only a few per cent of salts, not enough to interfere with its use. It is very bright, flexible and soluble in water. It is suitable for all applications of soluble threads such as the manufacture of artificial embroidery or the like. i
What is claimed is:
1. The method of producing spun yarns from aqueous solutions of polyvinyl alcohol which comprises spinning said solution into a concentrated aqueous saline solution, stretching the spun filaments during the spinning operation, winding the yarn thus produced onto a package, drying the package to produce a yarn having adherent powder thereon, and rewinding the yarn from said package while passing the yarn with the adherent powder thereon over stationary friction members to scrape the adherent powder from the surface thereof.
2. The method of producing spun yarns from aqueous solutions of polyvinyl alcohol which comprises spinning said solution into a concentrated aqueous saline solution, stretching the spun filaments during the spinning operation, winding the yarn thus produced onto a package, drying the package to produce a yarn havin adherent powder thereon, and rewinding the yarn from said package while passing the yarn with the adherent powder thereon over interleaved bars to apply friction to scrape the adherent'powder from the surface thereof. a
3.- The method of producing spun yarns from aqueous solutions of polyvinyl alcohol which comprises spinning said solution into a concentrated aqueous saline solution, stretching the spun filaments during the spinning operation, winding the yarn thus produced onto a package, drying the package at a slightly elevated temperature with circulation of air thereover to produce a yarn having adherent powder thereon, and rewinding the yarn from said package while passing the yarn with the adherent powder thereon over stationary friction members to scrape the adherent powder from the surface thereof.
4. The method of producingspun yarns from aqueous solutions of polyvinyl alcohol which comprises spinning said solution into a concentrated aqueous solution of ammonium sulphate, stretching the spun filaments during the spinning operation, winding the yarn thus produced onto a package, drying the package to provide a yarn having ammonium sulphate powdernadhering thereto, and rewinding the'yarn from said package while passing the yarn with the adherent powder thereon over stationary friction members to scrape the adherent powder from the surface thereof.
5. 'The method of producing spun yarns from aqueous solutions of polyvinyl alcohol which comprises spinning said solution into a concentrated aqueous saline solution, stretching the spun filaments during the spinning operation, winding the yarn thus produced onto a package, drying the package to produce a yarn havin adherent powder thereon, and rewinding the yarn from said package while" applying a stretching tension of approximately lgram per denier and scraping adherent powder from the surface thereof.
NICOLAS DRISCH. PAUL HERRBACH.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Houtz Nov. 6, 1945
Claims (1)
1. THE METHOD OF PRODUCING SPUN YARNS FROM AQUEOUS SOLUTIONS OF POLYVINYL ALCOHOL WHICH COMPRISES SPINNING SAID SOLUTION INTO A CONCENTRATED AQUEOUS SALINE SOLUTION, STRETCHING THE SPUN FILAMENTS DURING THE SPINNING OPERATION, WINDING THE YARN THUS PRODUCED ONTO A PACKAGE, DRYING THE PACKAGE TO PRODUCE A YARN HAVING ADHERENT POWDER THEREON, AND REWINDING THE YARN FROM SAID PACKAGE WHILE PASSING THE YARN WITH THE ADHERENT POWDER THEREON OVER STATIONARY FRICTION MEMBERS TO SCRAPE THE ADHERENT POWDER FROM THE SURFACE THEREOF.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR825581X | 1949-02-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2591242A true US2591242A (en) | 1952-04-01 |
Family
ID=9282397
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US139458A Expired - Lifetime US2591242A (en) | 1949-02-01 | 1950-01-19 | Process for the manufacture of yarns from hydroxylated polyvinyl compounds |
Country Status (7)
Country | Link |
---|---|
US (1) | US2591242A (en) |
BE (1) | BE492120A (en) |
CH (1) | CH284045A (en) |
DE (1) | DE825581C (en) |
FR (1) | FR983508A (en) |
GB (1) | GB667582A (en) |
NL (1) | NL73740C (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2716049A (en) * | 1951-11-01 | 1955-08-23 | Du Pont | Water-soluble yarn |
US2977183A (en) * | 1951-12-19 | 1961-03-28 | Air Reduction | Process of improving the dyeing properties of polyvinyl alcohol fibers |
US2994576A (en) * | 1954-09-09 | 1961-08-01 | Celanese Corp | Process for spinning polyvinyl alcohol filaments and remaining impurities therefrom |
US3511905A (en) * | 1967-08-22 | 1970-05-12 | Viscose Suisse Soc | Process for the preparation of synthetic polymer filaments |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5929146A (en) * | 1982-08-09 | 1984-02-16 | Kuraray Co Ltd | Preparation of water curable extrusion molded product |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2257382A (en) * | 1939-09-01 | 1941-09-30 | Warp Compressing Machine Compa | Yarn delivery arrangement for creels |
US2388325A (en) * | 1944-03-04 | 1945-11-06 | Du Pont | Spinning process for artificial filaments |
-
0
- NL NL73740D patent/NL73740C/xx active
- BE BE492120D patent/BE492120A/xx unknown
-
1949
- 1949-02-01 FR FR983508D patent/FR983508A/en not_active Expired
-
1950
- 1950-01-03 GB GB158/50A patent/GB667582A/en not_active Expired
- 1950-01-14 DE DEC417A patent/DE825581C/en not_active Expired
- 1950-01-17 CH CH284045D patent/CH284045A/en unknown
- 1950-01-19 US US139458A patent/US2591242A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2257382A (en) * | 1939-09-01 | 1941-09-30 | Warp Compressing Machine Compa | Yarn delivery arrangement for creels |
US2388325A (en) * | 1944-03-04 | 1945-11-06 | Du Pont | Spinning process for artificial filaments |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2716049A (en) * | 1951-11-01 | 1955-08-23 | Du Pont | Water-soluble yarn |
US2977183A (en) * | 1951-12-19 | 1961-03-28 | Air Reduction | Process of improving the dyeing properties of polyvinyl alcohol fibers |
US2994576A (en) * | 1954-09-09 | 1961-08-01 | Celanese Corp | Process for spinning polyvinyl alcohol filaments and remaining impurities therefrom |
US3511905A (en) * | 1967-08-22 | 1970-05-12 | Viscose Suisse Soc | Process for the preparation of synthetic polymer filaments |
Also Published As
Publication number | Publication date |
---|---|
CH284045A (en) | 1952-07-15 |
DE825581C (en) | 1951-12-20 |
NL73740C (en) | |
FR983508A (en) | 1951-06-25 |
BE492120A (en) | |
GB667582A (en) | 1952-03-05 |
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