US2432085A - Viscose spinning solutions - Google Patents

Viscose spinning solutions Download PDF

Info

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
Application number
US516240A
Inventor
Rudolph S Bley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
North American Rayon Corp
Original Assignee
North American Rayon Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US233824A external-priority patent/US2345570A/en
Application filed by North American Rayon Corp filed Critical North American Rayon Corp
Priority to US516240A priority Critical patent/US2432085A/en
Application granted granted Critical
Publication of US2432085A publication Critical patent/US2432085A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
US516240A 1938-10-07 1943-12-30 Viscose spinning solutions Expired - Lifetime US2432085A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (7)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US2179196A (en) Manufacture of artificial silk
US2345570A (en) Coagulating bath containing cationactive inhibitors
US2310207A (en) Surface-active incrustation inhibitor
GB281351A (en) Manufacture of artificial materials from viscose
GB654083A (en) Spinning of viscose
US2393817A (en) Production of cellulosic products
US2145857A (en) Fibroin spinning solution
GB978149A (en)
EP0996777B1 (en) Use of an amphoteric surfactant as a viscose spin bath additive
US2145580A (en) Spinning solutions containing organic dyes and products thereof
US2397338A (en) Manufacture of filaments and fibers
US3007766A (en) Production of viscose rayon
US2294378A (en) Surface-active incrustation inhibitor
USRE23013E (en) Method of improving the processing
GB554689A (en) Improvements in or relating to the manufacture of regenerated cellulose yarns, filaments, films and the like
US2302589A (en) Production of thread from viscose
US2348203A (en) Viscose spinning solution
EP1036224B1 (en) Use of an alkoxylated polyamine surfactant as a viscose spin bath additive
US2286962A (en) Manufacture and production of artificial threads and the like articles
US2336778A (en) Treatment of acid setting baths used in the manufacture of cellulose products from viscose
US2462948A (en) Flotation process of clarifying regenerating baths
US2623874A (en) Cellulose-morpholinium derivative composition and process
US1045731A (en) Manufacture of threads, filaments, strips, or films of cellulose.
GB903205A (en) Chemical additive for use in the production of regenerated cellulose products
US3041132A (en) Spinning of viscose