US2432085A - Viscose spinning solutions - Google Patents
Viscose spinning solutions Download PDFInfo
- Publication number
- US2432085A US2432085A US516240A US51624043A US2432085A US 2432085 A US2432085 A US 2432085A US 516240 A US516240 A US 516240A US 51624043 A US51624043 A US 51624043A US 2432085 A US2432085 A US 2432085A
- Authority
- US
- United States
- Prior art keywords
- viscose
- cation
- spinning
- radicals
- active
- 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 20
- 238000009987 spinning Methods 0.000 title description 15
- -1 aliphatic acyl radical Chemical class 0.000 description 25
- 239000000243 solution Substances 0.000 description 17
- 239000003112 inhibitor Substances 0.000 description 9
- 150000001450 anions Chemical class 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 125000005263 alkylenediamine group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 150000005840 aryl radicals Chemical group 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 3
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000004627 regenerated cellulose Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000001112 coagulating effect Effects 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000008233 hard water Substances 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 150000003752 zinc compounds Chemical class 0.000 description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
- 239000011686 zinc sulphate Substances 0.000 description 2
- 235000009529 zinc sulphate Nutrition 0.000 description 2
- 240000000146 Agaricus augustus Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- PGTXKIZLOWULDJ-UHFFFAOYSA-N [Mg].[Zn] Chemical compound [Mg].[Zn] PGTXKIZLOWULDJ-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000012435 aralkylating agent Substances 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 235000016804 zinc Nutrition 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
-
- 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
- D01F2/10—Addition to the spinning solution or spinning bath of substances which exert their effect equally well in either
Definitions
- R represents an aliphatic acyl radical having 8 or more carbon atoms
- R1 represents a hydrogen atom or an acyl, alkyl, aryl or aralkyl radical
- R2, R3 and R4 represent alkyl and/or aryl and/or aralkyl radicals
- n is a whole number
- X represents an innocuous anion.
- Cation-active compounds are surface-activecompounds which carry in the cation a hydrocarbon chain having 8 or more carbon atoms. They are particularly advantageous because they may be used in neutral salt, alkaline and acidic aqueous solutions, and also in hard water.
- anion-active compounds are surface-active compounds Which carry in the anion a more or less extended hydrocarbon chain. They flocculate in neutral salt, alkaline and acidic aqueous solutions, and also in hard water. Common soaps, sulphonated oils, etc., are anion-active compounds, and thus they are unable to prevent the incrustation of spinnerets and spinneret orifices.
- Incrustation inhibitors in accordance with the present invention, may be prepared by causing high-molecular, mono-acylated or unsymmetrical diacylated alkylenediamines with alkylating, arylating or aralkylating agents, such as dimethyl sulphate, methyl iodide, methyl bromide,
- acetylated or acylated alkylenediamines may be prepared in accordance with processes set forth in U. S. Patent No. 1,534,525.
- these cation-active incrustation inhibitors may form corresponding bases in viscose solutions and salts in acid spin baths, they retain their surface-activity and, thus, their property of substantially preventing incrustations on prolonged spinning. If very small amounts of these cation-active compounds are added to viscose solutions or spin baths the physical characteristics, such as strength, plasticity, lustre, etc., of regenerated cellulose produced therefrom or therein, respectively, remain unaltered. Upon increasing the amount of incrustation inhibitor in a given viscose solution or spin bath, the regenerated cellulose produced therefrom or therein, respectively, may alter its physical characteristics, i. e., it may acquire a soft-lustre, become more plastic, lose part of its original strength etc.
- Example I About 380 parts of oleyl-diethyl-ethylene-die amine are reacted with about 126 parts of dimethylsulphate, About 0.3 to 2.0 grams of the oily mono oleyl diethyl-methylethylene-diammonium-methyl-sulphate are added to about one liter of a viscose solution of conventional cellulose content and maturity. This solution is then extruded through a spinneret into a conventional spin bath, such as, for example, a glucose bath, a magnesium zinc bath, etc. The spinnerets and their princes remain clean on prolonged spinning.
- a spinneret such as, for example, a glucose bath, a magnesium zinc bath, etc.
- Example II About 382 parts of stearyl-diethyl-ethylene diamine are melted and reacted with about 126 parts of dimethyl sulphate. The soapy mass is probably mono-stearyl-diethyl-methylethylenediammonium-methyl-sulphate.
- a conventional viscose solution is extruded through fine orifices of precious metal spinnerets into an acid spin bath, containing for example, sulphuric acid, sodium sulphate, ammonium sulphate and zinc sulphate and about 0.3 to 5.0 grams per liter of mono-stearyl-diethyl-methylethylene diammonium-methyl-sulphate, Spinning difiiculties and irregularities are substantially overcome. Without the addition of an incrustation inhibitor spinning is'interrupted after a very short period of time.
- This inhibitor may be replaced by similar derivatives obtained from 1auryl-diethylenediamine, octancyl-diethylenediamine, lauryl-dipropylenediamine, octanoyl-di propylenediamine, etc.
- Example III 360 parts of oleyl-diethylethylene-diamine are reacted with about 142 parts of benzyl chloride.
- the resulting oily product probably mono-oleyldiethyl-benzylethylene-diammonium-chloride, is added to both the viscose solution and the spin bath.
- the formation of zinc rings and sulphur craters is substantially overcome.
- R represents an aliphatic acyl radical having 8 or more carbon atoms
- R1 represents a hydrogen atom or an acyl, alkyl, aryl or aralkyl radical
- R2, R3 and R4 represent alkyl and/or aryl and/or aralkyl radicals
- n is a whole num* her
- X represents an innocuous anion, provided' it is sufiiciently soluble and stable in spin baths and/or viscose solutions to furnish surfaceactive cations therein.
- a viscose spinning so ution containing a dissolved, substantially stable, cation-active alkylene derivative having the structure:
- R represents an aliphatic acyl radical having 8 or more carbon atoms
- R1 represents a substituent selected from the group consisting of hydrogen, acyl radicals, alkyl radicals, aryl radicals and aralkyl radicals
- R2, R3 and R4 represent alkyl radicals
- n is a whole number
- X represents an innocuous anion.
- a viscose spinning solution containing a dissolved, substantially stable, cation-active alkylene derivative having the structure:
- R represents an aliphatic acyl radical having 8 or more carbon atoms
- R1 represents a substituent selected from the group consisting of hydrogen, acyl radicals, alkyl radicals, aryl radicals and aralkyl radicals
- R2, R3 and R4 represent aryl radicals
- n is a whole number
- X represents an innocuous anion.
- R represents an aliphatic acyl radical having 8 or more carbon atoms
- R1 represents a substituent selected from the group consisting of hydrogen, acyl radicals, alkyl radicals, aryl radicals and aralkyl radicals
- R2, R3 and R4 represent aralkyl radicals
- n is a whole number
- X represents an innocuous anion.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
Description
Patented Dec. 9, 1947 VISCOSE SPINNING SOLUTIONS Rudolph S. Bley, Milligan College, Tenn, assignor to North American Rayon Corporation, New York, N. Y., a corporation of Delaware No Drawing.
Original application October 7,
1938, Serial No. 233,824. Divided and this application December 30, 1943, Serial No. 516,240
4 Claims.
In the manufacture of cellulosic products, such as filaments, and the like, a viscose solution is continuously extruded through the minute orifices.of a spinneret into a coagulating bath (setting bath). However, since the introduction of the viscose process great troubles have been and are still experienced as far as continuous spinning is concerned due to impurities, such as, for example, precipitated cellulose particles, sulphur and resin particles, zinc compounds, etc., present in either the viscose solution or the spin bath. These impurities gradually contaminate the spinnerets, clog and reduce the widths of the spinneret orifices with the result that filaments of uneven thickness are obtained. If contamination proceeds the individual filaments start to tear and occasion interruption of the spinning process.
I have found that contamination of spinnerets and clogging of spinneret holes (orifices) may be substantially overcome by spinning viscose solutions in the presence of cation-active substances or acid addition products thereof having the general structure:
in which R represents an aliphatic acyl radical having 8 or more carbon atoms, R1 represents a hydrogen atom or an acyl, alkyl, aryl or aralkyl radical, R2, R3 and R4 represent alkyl and/or aryl and/or aralkyl radicals, n is a whole number, and X represents an innocuous anion.
Cation-active compounds are surface-activecompounds which carry in the cation a hydrocarbon chain having 8 or more carbon atoms. They are particularly advantageous because they may be used in neutral salt, alkaline and acidic aqueous solutions, and also in hard water. In contradistinction to cation-active compounds, anion-active compounds are surface-active compounds Which carry in the anion a more or less extended hydrocarbon chain. They flocculate in neutral salt, alkaline and acidic aqueous solutions, and also in hard water. Common soaps, sulphonated oils, etc., are anion-active compounds, and thus they are unable to prevent the incrustation of spinnerets and spinneret orifices.
Incrustation inhibitors, in accordance with the present invention, may be prepared by causing high-molecular, mono-acylated or unsymmetrical diacylated alkylenediamines with alkylating, arylating or aralkylating agents, such as dimethyl sulphate, methyl iodide, methyl bromide,
phenyl bromide, p-toluene-ethyl sulphonate, etc.
The acetylated or acylated alkylenediamines may be prepared in accordance with processes set forth in U. S. Patent No. 1,534,525.
Although these cation-active incrustation inhibitors may form corresponding bases in viscose solutions and salts in acid spin baths, they retain their surface-activity and, thus, their property of substantially preventing incrustations on prolonged spinning. If very small amounts of these cation-active compounds are added to viscose solutions or spin baths the physical characteristics, such as strength, plasticity, lustre, etc., of regenerated cellulose produced therefrom or therein, respectively, remain unaltered. Upon increasing the amount of incrustation inhibitor in a given viscose solution or spin bath, the regenerated cellulose produced therefrom or therein, respectively, may alter its physical characteristics, i. e., it may acquire a soft-lustre, become more plastic, lose part of its original strength etc. For such reasons, the amounts to be added to viscose solutions and/or spin baths must be predetermined by experimentation. Additions of about 0.1 to 5.0 grams per liter of viscose solution or spin bath are generally sufiicient to allow continuous spinning without substantially affecting the inherent physical characteristics of regenerated cellulose threads, films, etc. Although these cation-active incrustation inhibitors improve the spinning of any conventional viscose solution or spin bath, I have found that they are especially valuable as additions to zinc-bearing spin baths, 1'. e., spin bathscontaining a soluble zinc compound, for example; zinc sulphate, these baths, having poor spinning qualities. I am well aware that cation-active alkylene diamines have, heretofore, been prepared as wetting agents. However, the prior art does not disclose the use of these derivatives as incrustation inhibitors, the object of the present invention.
Example I About 380 parts of oleyl-diethyl-ethylene-die amine are reacted with about 126 parts of dimethylsulphate, About 0.3 to 2.0 grams of the oily mono oleyl diethyl-methylethylene-diammonium-methyl-sulphate are added to about one liter of a viscose solution of conventional cellulose content and maturity. This solution is then extruded through a spinneret into a conventional spin bath, such as, for example, a glucose bath, a magnesium zinc bath, etc. The spinnerets and their princes remain clean on prolonged spinning.
3 Other cation-active alkylenediamine derivatives having the general structure set forth above may be used with equal success.
Example II About 382 parts of stearyl-diethyl-ethylene diamine are melted and reacted with about 126 parts of dimethyl sulphate. The soapy mass is probably mono-stearyl-diethyl-methylethylenediammonium-methyl-sulphate.
A conventional viscose solution is extruded through fine orifices of precious metal spinnerets into an acid spin bath, containing for example, sulphuric acid, sodium sulphate, ammonium sulphate and zinc sulphate and about 0.3 to 5.0 grams per liter of mono-stearyl-diethyl-methylethylene diammonium-methyl-sulphate, Spinning difiiculties and irregularities are substantially overcome. Without the addition of an incrustation inhibitor spinning is'interrupted after a very short period of time. This inhibitor may be replaced by similar derivatives obtained from 1auryl-diethylenediamine, octancyl-diethylenediamine, lauryl-dipropylenediamine, octanoyl-di propylenediamine, etc.
Example III 360 parts of oleyl-diethylethylene-diamine are reacted with about 142 parts of benzyl chloride. The resulting oily product, probably mono-oleyldiethyl-benzylethylene-diammonium-chloride, is added to both the viscose solution and the spin bath. The formation of zinc rings and sulphur craters is substantially overcome.
Although these examples will serve to illustrate the present invention. I do not wish to be limited to the incrustation inhibitors and concentrations thereof recited therein, since I may make use of any cation-active alkylene derivative and acid addition products thereof having the structure:
in which R represents an aliphatic acyl radical having 8 or more carbon atoms, R1 represents a hydrogen atom or an acyl, alkyl, aryl or aralkyl radical, R2, R3 and R4 represent alkyl and/or aryl and/or aralkyl radicals, n is a whole num* her, and X represents an innocuous anion, provided' it is sufiiciently soluble and stable in spin baths and/or viscose solutions to furnish surfaceactive cations therein. Modifications of my invention will readily be recognized by those skilled in the art, and I desire to include all such modifications coming within the scope of the appended claims.
This is a division of my copending application, Ser. No. 233,824, filed October 7, 1938, Patent No. 2,345,570, entitled Coagulating bath containing cation-active inhibitors.
I claim:
1. A viscose spinning so ution containing a dissolved, substantially stable, cation-active alkylene derivative having the structure:
in which R represents an aliphatic acyl radical having 8 or more carbon atoms, R1 represents a substituent selected from the group consisting of hydrogen, acyl radicals, alkyl radicals, aryl radicals and aralkyl radicals, R2, R3 and R4 represent alkyl radicals, n is a whole number and X represents an innocuous anion.
3. A viscose spinning solution containing a dissolved, substantially stable, cation-active alkylene derivativehaving the structure:
in which R represents an aliphatic acyl radical having 8 or more carbon atoms, R1 represents a substituent selected from the group consisting of hydrogen, acyl radicals, alkyl radicals, aryl radicals and aralkyl radicals, R2, R3 and R4 represent aryl radicals, n is a whole number and X represents an innocuous anion.
4'. A viscose spinning solution containing a dissolved, substantially stable, cation active alkylene derivative having the structure:
m lb
in which R represents an aliphatic acyl radical having 8 or more carbon atoms, R1 represents a substituent selected from the group consisting of hydrogen, acyl radicals, alkyl radicals, aryl radicals and aralkyl radicals, R2, R3 and R4 represent aralkyl radicals, n is a whole number and X represents an innocuous anion.
RUDOLPH S. BLEY.
REFERENCES CITED The following references are of record in thc file of this patent:
UNITED STATES PATENTS Number Name Date 2,345,570 Bley Apr. 4, 1944 2,125,031 Polak et, a1. July 26, 1938 2,310,208 Bley Feb. 9, 1943 2,310,207 Bley Feb. 9, 1943 2,294,379 Bley Sept. 1, 1942 2,294,378 Bley Sept. 1, 1942 2,132,930 Bley Oct. 11, 1938
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US516240A US2432085A (en) | 1938-10-07 | 1943-12-30 | Viscose spinning solutions |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US233824A US2345570A (en) | 1938-10-07 | 1938-10-07 | Coagulating bath containing cationactive inhibitors |
| US516240A US2432085A (en) | 1938-10-07 | 1943-12-30 | Viscose spinning solutions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2432085A true US2432085A (en) | 1947-12-09 |
Family
ID=26927259
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US516240A Expired - Lifetime US2432085A (en) | 1938-10-07 | 1943-12-30 | Viscose spinning solutions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2432085A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2792281A (en) * | 1953-09-21 | 1957-05-14 | American Viscose Corp | Viscose composition and method of spinning |
| US2884332A (en) * | 1953-04-30 | 1959-04-28 | Saul & Co | Printing of textile materials and preparations therefor |
| US2910341A (en) * | 1953-11-09 | 1959-10-27 | Du Pont | Spinning viscose |
| US2950217A (en) * | 1956-11-13 | 1960-08-23 | Du Pont | Impregnation process |
| US3252816A (en) * | 1962-05-28 | 1966-05-24 | Allied Chem | Pigmented extrudable viscose solutions |
| US3298962A (en) * | 1960-12-29 | 1967-01-17 | Gen Aniline & Film Corp | Spin bath additives |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2125031A (en) * | 1935-02-16 | 1938-07-26 | American Enka Corp | Manufacture of artificial silk |
| US2132930A (en) * | 1937-12-02 | 1938-10-11 | North American Rayon Corp | Viscose spinning solution |
| US2294379A (en) * | 1938-10-07 | 1942-09-01 | North American Rayon Corp | Surface-active incrustation inhibitor |
| US2294378A (en) * | 1940-01-29 | 1942-09-01 | North American Rayon Corp | Surface-active incrustation inhibitor |
| US2345570A (en) * | 1938-10-07 | 1944-04-04 | North American Rayon Corp | Coagulating bath containing cationactive inhibitors |
-
1943
- 1943-12-30 US US516240A patent/US2432085A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2125031A (en) * | 1935-02-16 | 1938-07-26 | American Enka Corp | Manufacture of artificial silk |
| US2132930A (en) * | 1937-12-02 | 1938-10-11 | North American Rayon Corp | Viscose spinning solution |
| US2294379A (en) * | 1938-10-07 | 1942-09-01 | North American Rayon Corp | Surface-active incrustation inhibitor |
| US2310208A (en) * | 1938-10-07 | 1943-02-09 | North American Rayon Corp | Surface-active incrustation inhibitor |
| US2310207A (en) * | 1938-10-07 | 1943-02-09 | North American Rayon Corp | Surface-active incrustation inhibitor |
| US2345570A (en) * | 1938-10-07 | 1944-04-04 | North American Rayon Corp | Coagulating bath containing cationactive inhibitors |
| US2294378A (en) * | 1940-01-29 | 1942-09-01 | North American Rayon Corp | Surface-active incrustation inhibitor |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2884332A (en) * | 1953-04-30 | 1959-04-28 | Saul & Co | Printing of textile materials and preparations therefor |
| US2792281A (en) * | 1953-09-21 | 1957-05-14 | American Viscose Corp | Viscose composition and method of spinning |
| US2910341A (en) * | 1953-11-09 | 1959-10-27 | Du Pont | Spinning viscose |
| US2950217A (en) * | 1956-11-13 | 1960-08-23 | Du Pont | Impregnation process |
| US3298962A (en) * | 1960-12-29 | 1967-01-17 | Gen Aniline & Film Corp | Spin bath additives |
| US3252816A (en) * | 1962-05-28 | 1966-05-24 | Allied Chem | Pigmented extrudable viscose solutions |
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