US2359749A - Manufacture of synthetic yarns and the like - Google Patents
Manufacture of synthetic yarns and the like Download PDFInfo
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- US2359749A US2359749A US389325A US38932541A US2359749A US 2359749 A US2359749 A US 2359749A US 389325 A US389325 A US 389325A US 38932541 A US38932541 A US 38932541A US 2359749 A US2359749 A US 2359749A
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- per molecule
- polyoxyethylene
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- oxyethylene
- oxyethylene units
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- 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
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- 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
- This invention relates to improvements in the manufacture of synthetic yarns, filaments, films and the like. More particularly, the invention relates to improvements in the spinning operation employed in the manufacture of synthetic yarns, filaments, films and the like.
- a solution is generally first prepared of the material to com prise the shape.
- the shape is formed or spun by extruding the solution through a spinneret or jet having a minute opening or openings into a coagulating or precipitating medium.
- obstructions tend to form in the minute openings in the spinneret or jet and they become fouled or clogged. This results, in the case of yarn or filament spinning, in a lack of uniformity in the filament sizes and weak and broken filaments in the finished product and, in the case of producing films, in a lack of uniformity in thickness.
- This invention has for its principal object to provide improvements in the spinning operation employed in the manufacture of synthetic shapes such as yarns, filaments, films and the like.
- the compounds contemplated by the invention are the polyethylene glycol ethers of organic compounds having at least one func tional aliphatic hydroxyl group and containing at least one hydrophobic group comprising a hydrocarbon chain of at least 8 carbon atoms, such as alcohols and polyhydric alcohols, hydroxycaroxylic aicds, hydroxy esters, epoxy alcohols and hydroxy epoxy esters; polyethylene glycol esters of compounds having at least one functional aliphatic carboxyl group and containing at least one hydrophobic group comprising a.
- hydrocarbon chain of at least 8 carbon atoms such as fatty acids, polycarboxylic acids, hydroxy fatty acids, and epoxy fatty acids; polyethylene glycol acetals of organic compounds having at least one functional aliphatic aldehyde group and containing at least one hydrophobic group comprising a hydrocarbon chain of at least 8 carbon atoms, such as aliphatic aldehydes, aldoses; and polyethylene glycol ether-esters, ether-acetals, ester-acetals or ether-ester-acetals of organic compounds having various combinations of hydroxyl, aldehyde and carboxyl groups and containing at least one hydrophobic group comprising a hydrocarbon chain of at least 8 carbon atoms, such as hydroxy fatty acids, polyhydroxy fatty acids, aldoses, and -uronic acids.
- the compounds are non-ionogenic, relatively chemically unreactive, substantially stable under spinning conditions, and contain no free functional groups other than aliphatic hydroxyl or carbonyl.
- the compounds may contain ether, ester, acetal, or hemiacetal groups which are substantially stable under the conditions of spinning.
- the stability herein referred to is such stability that the compounds, prior to their complete decomposition in the spinning solution or the spinning bath, will exert their favorable influence in preventing clogging of the openings in the spinnerets and in thereby maintaining uniformity of filament size.
- Hydroxy stearic acid esters of polyoxyethylene glycols Octyl ethers of polyoxyethylene glycols Decyl ethers of polyoxyethylene glycols Dodecyl ethers of polyoxyethylene glycols Tetradecyl ethers of polyoxyethylene glycols Hexadecyl ethers of polyoxyethylene glycols Octadecyl ethers of polyoxyethylene glycols Cetyl ethers of polyoxyethylene glycols Montanyl ethers of polyoxyethylene glycols Oleyl ethers of polyoxyethylene glycols Polyoxyethylene glycol ethers of ethylene glycol monoacyl 1 esters Polyoxyethylene glycol ethers of diethylene glycol monoacyl esters Polyoxyethylene glycol ethers of polyethylene The polyethylene glycol group or groups may be connected in the same compound by either or both ether and ester groups depending upon the parent substances from which they are derived and the method of producing the compounds therefrom.
- acyl esters may be the esters of fatty acids having 8 carbon atoms in a straight chain, such as caprylic, pelargonic, capric, lauri
- the oxyethylene units may replace the hydrogen of the hydroxyl group while another part may replace the hydrogen of the carboxyl group, thereby producing polyoxyethylene ether-esters.
- all of the oxyethylene units may be in a single chain or they may be present in the compound in the form of two or more chains, the latter situation being common when the compound is produced by reacting ethylene oxide with a parent substance having at least two functional groups whether hydroxyl, aldehyde, carboxyl or any combination of these three. It is only essential. that the total number of oxyethylene units in the one or more chains add up to a total of at least eight. Some or all of the oxyethylene units or chains of such units may have either or both of their ends connected to the remainder of the compound through ether, ester or acetal linkages.
- the common methods of making the compounds with which the invention is concerned generally result in the formation of mixtures of compounds having a greater or less number of oxyethylene units per molecule and analytical determinations of such complex mixtures indicate the average number of such units per molecule throughout the mass of the compound analyzed.
- the compounds employed in accordance with this invention may comprise molecules containing less than 8 oxyethylene units in admixture with other containing 8 or more the claims the definition of these compounds is intended to include not only those having a uniform and constant constitution throughout but also such complex mixtures as have an efiective portion containing at least 8 oxyethylene units per molecule.
- the various surface active compounds may be produced in any suitable manner. Generally, they may be produced by reacting ethylene oxide with the selected fatty acid, alcohol, hydroxy fatty acid, hydroxy fatty acid ester or related compound within the scope of the general class described above.
- the reaction products of ethylene oxide with sorbitan monolaurate may be prepared by introducing sorbitan monolaurate with a small amount of sodium methylate as a, catalyst into a stirring autoclave and raising the temperature to C., gradually adding ethylene oxide to this mixture and maintaining the temperature between C. and C.
- the degree to which the reaction with the ethylene oxide is carried out depends upon the compound with which it is reacted and the character of the spinning solution or precipitating bath in which it is to be used. The reaction is carried out to such a degree that the reaction products are soluble in the spinning bath or spinning solution in which they are used.
- the invention is applicable in forming regenerated cellulose shapes by extruding viscose solution into an acid precipitating bath and is found particularly advantageous where the precipitating bath contains a high concentration of metallic salts, especially zinc, in concentrations of Accordingly, in the specification and the order of 3% to
- the invention is also advantageous in spinning other cellulose solutions including cuprammonium and cellulose derivatives such as cellulose acetate as well as other synthetic materials, including copolymers of vinyl chloride and vinyl acetate.
- a small amount of the surface active material of the order of 0.01 to 0.05 may be dissolved in the spinning solution and the spinning solution is extruded into a precipitating medium.
- a small amount of the surface active material of the same order may be dissolved in the precipitating medium or may be added to both the spinning solution and the precipitating medium.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% or organic compounds comprising sorbitan monolaurate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethlene content of oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a sorbitan monolaurate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 8 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a sorbitan monooleate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monomyristate having at least 1 hydroxy polyoxyethylene group per molecule and an avdroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monopalmitate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% organic compounds comprising a mannitan monostearate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc'sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising lauryl alcohol in which the hydroxyl group has been replaced by a hydroxy polyoxyethylene group and the average oxyethylene content is 20 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monolaurate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
- a multifilament regenerated cellulose yarn is formed by extruding a viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monooleate having at least 1 hyl6 10.
- a multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising triricinolein in which at least 1 free hydroxyl group has been replaced by a hydroxy polyoxyethylene group and the average oxyethylene content is 20 oxyethylene units per molecule.
- An aqueous acid medium for precipitating viscose in the form of filaments, films and the like containing a small amount of a dissolved ester of a polyhydric alcohol having a hydrophobic group containing at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
- oxyethylene content being at least 8 oxyethylene units per molecule.
- An aqueous medium for precipitating viscose in the form of filaments, films and the like containing sulfuric acid and a small amount of a dissolved substantially stable surface active non-ionogenic polyethylene glycol ether of a partially esterified polyhydric alcohol containing an epoxy group, said esterified polyhydric alcohol containing a hydrophobic radical having a hydrocarbon chain of at least 8 carbon atoms and said ether containing at least 8 oxyethylene units per molecule.
- An aqueous medium for precipitating viscose in the form of filaments, films and the like containing sulfuric acid, a zinc salt and a small amount of a dissolved substantially stable surface active non-ionogenic polyethylene glycol ether of a partially esterified polyhydric alco hol containing an epoxy group, said esterified polyhydric alcohol containing a hydrophobic radical having a hydrocarbon chain of at least 8 carbon atoms and said ether containing at least 8 oxyethylene units per molecule.
- An aqueous medium for precipitating viscose in the form of filaments, films and the like containing sulfuric acid, a zinc salt and a small amount of a dissolved substituted hexitan having a hydrophobic group containing at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
- An aqueous medium for precipitating viscose in the form of filaments, films and the like containing sulfuric acid, a zinc salt and a small amount of a substituted mannitan monostearate having at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Description
Patented Oct. 10, 1944 MANUFACTURE OF SYNTHETIC YARNS AND THE LIKE Benjamin W. Collins, Swarthmore, Pa.
No Drawing. Application April 19, 1941, Serial No. 889,325
15 Claims. (Cl. 18-54) This invention relates to improvements in the manufacture of synthetic yarns, filaments, films and the like. More particularly, the invention relates to improvements in the spinning operation employed in the manufacture of synthetic yarns, filaments, films and the like.
In the manufacture of synthetic shapes such as yarns, filaments, films and the like, a solution is generally first prepared of the material to com prise the shape. The shape is formed or spun by extruding the solution through a spinneret or jet having a minute opening or openings into a coagulating or precipitating medium. During the spinning operation obstructions tend to form in the minute openings in the spinneret or jet and they become fouled or clogged. This results, in the case of yarn or filament spinning, in a lack of uniformity in the filament sizes and weak and broken filaments in the finished product and, in the case of producing films, in a lack of uniformity in thickness. In order to avoid these difliculties it is the present practice to inspect the spinnerets or jets at short intervals of time and replace those in which the openings have become fouled. This interrupts the continuity of the spinning operation and causes delays which are time consuming and costly.
This invention has for its principal object to provide improvements in the spinning operation employed in the manufacture of synthetic shapes such as yarns, filaments, films and the like.
Other objects of the invention will be apparent from the following description and appended claims.
It has now been found that fouling of the spinnerets and the need for frequent inspection and replacement and the lack of uniformity in yarns, filaments and films can be largely elimiminated by extruding the spinning solution in the presence of a small amount of a surface active, non-ionogenic organic compound comprising at least one hydrophobic group having a hydrocarbon'chain of at least ,8 carbon atoms and a hydrophilic polyoxyethylene content sufficient to render the compound water-soluble so that it is readily soluble in the spinning bath or in the spinning solution. The polyoxyethylene content should be at least 8 oxyethylene units per molecule. Generally, the greater the extent to which the compound is hydrophobic, the larger the number of oxyethylene units that are required to render the compound sufiiciently soluble for the purposes of the invention.
In general, the compounds contemplated by the invention are the polyethylene glycol ethers of organic compounds having at least one func tional aliphatic hydroxyl group and containing at least one hydrophobic group comprising a hydrocarbon chain of at least 8 carbon atoms, such as alcohols and polyhydric alcohols, hydroxycaroxylic aicds, hydroxy esters, epoxy alcohols and hydroxy epoxy esters; polyethylene glycol esters of compounds having at least one functional aliphatic carboxyl group and containing at least one hydrophobic group comprising a. hydrocarbon chain of at least 8 carbon atoms, such as fatty acids, polycarboxylic acids, hydroxy fatty acids, and epoxy fatty acids; polyethylene glycol acetals of organic compounds having at least one functional aliphatic aldehyde group and containing at least one hydrophobic group comprising a hydrocarbon chain of at least 8 carbon atoms, such as aliphatic aldehydes, aldoses; and polyethylene glycol ether-esters, ether-acetals, ester-acetals or ether-ester-acetals of organic compounds having various combinations of hydroxyl, aldehyde and carboxyl groups and containing at least one hydrophobic group comprising a hydrocarbon chain of at least 8 carbon atoms, such as hydroxy fatty acids, polyhydroxy fatty acids, aldoses, and -uronic acids. The compounds are non-ionogenic, relatively chemically unreactive, substantially stable under spinning conditions, and contain no free functional groups other than aliphatic hydroxyl or carbonyl. The compounds may contain ether, ester, acetal, or hemiacetal groups which are substantially stable under the conditions of spinning. The stability herein referred to is such stability that the compounds, prior to their complete decomposition in the spinning solution or the spinning bath, will exert their favorable influence in preventing clogging of the openings in the spinnerets and in thereby maintaining uniformity of filament size.
The following are examples of specific compounds that may be used in carrying out this invention:
Hydroxy stearic acid esters of polyoxyethylene glycols Octyl ethers of polyoxyethylene glycols Decyl ethers of polyoxyethylene glycols Dodecyl ethers of polyoxyethylene glycols Tetradecyl ethers of polyoxyethylene glycols Hexadecyl ethers of polyoxyethylene glycols Octadecyl ethers of polyoxyethylene glycols Cetyl ethers of polyoxyethylene glycols Montanyl ethers of polyoxyethylene glycols Oleyl ethers of polyoxyethylene glycols Polyoxyethylene glycol ethers of ethylene glycol monoacyl 1 esters Polyoxyethylene glycol ethers of diethylene glycol monoacyl esters Polyoxyethylene glycol ethers of polyethylene The polyethylene glycol group or groups may be connected in the same compound by either or both ether and ester groups depending upon the parent substances from which they are derived and the method of producing the compounds therefrom. For example, if ricinoleic acid, hydroxy stearic acid or other bifunctional compounds are reacted with ethylene oxide, part of Polyoxyethylene glycol ethers of sorbitan acyl partial esters Polyoxyethylene glycol ethers of hexide acyl partial esters Polyoxyethylene glycol ethers of mannide acyl partial esters Polyoxyethylene glycol ethers of sorbide acyl partial esters Polyoxyethylene glycol ethers of cyclotol acyl partial esters Polyoxyethylene glycol ethers of inositol acyl partial esters Polyoxyethylene glycol ethers of monosaccharide acyl partial esters Polyoxyethylene glycol ethers of oligosaccharide acy1 partial esters of mannitan of mannitan ethers of mannitan 1 The acyl esters may be the esters of fatty acids having 8 carbon atoms in a straight chain, such as caprylic, pelargonic, capric, lauric, myristic, palinitic, margaric, stearic, oleic, ricinoleic, and hydroxy stearic.
such units.
the oxyethylene units may replace the hydrogen of the hydroxyl group while another part may replace the hydrogen of the carboxyl group, thereby producing polyoxyethylene ether-esters.
It should be noted that all of the oxyethylene units may be in a single chain or they may be present in the compound in the form of two or more chains, the latter situation being common when the compound is produced by reacting ethylene oxide with a parent substance having at least two functional groups whether hydroxyl, aldehyde, carboxyl or any combination of these three. It is only essential. that the total number of oxyethylene units in the one or more chains add up to a total of at least eight. Some or all of the oxyethylene units or chains of such units may have either or both of their ends connected to the remainder of the compound through ether, ester or acetal linkages.
The common methods of making the compounds with which the invention is concerned generally result in the formation of mixtures of compounds having a greater or less number of oxyethylene units per molecule and analytical determinations of such complex mixtures indicate the average number of such units per molecule throughout the mass of the compound analyzed. For this reason the compounds employed in accordance with this invention may comprise molecules containing less than 8 oxyethylene units in admixture with other containing 8 or more the claims the definition of these compounds is intended to include not only those having a uniform and constant constitution throughout but also such complex mixtures as have an efiective portion containing at least 8 oxyethylene units per molecule.
The various surface active compounds may be produced in any suitable manner. Generally, they may be produced by reacting ethylene oxide with the selected fatty acid, alcohol, hydroxy fatty acid, hydroxy fatty acid ester or related compound within the scope of the general class described above. For example, the reaction products of ethylene oxide with sorbitan monolaurate may be prepared by introducing sorbitan monolaurate with a small amount of sodium methylate as a, catalyst into a stirring autoclave and raising the temperature to C., gradually adding ethylene oxide to this mixture and maintaining the temperature between C. and C. For reasons stated above, the degree to which the reaction with the ethylene oxide is carried out depends upon the compound with which it is reacted and the character of the spinning solution or precipitating bath in which it is to be used. The reaction is carried out to such a degree that the reaction products are soluble in the spinning bath or spinning solution in which they are used.
The invention is applicable in forming regenerated cellulose shapes by extruding viscose solution into an acid precipitating bath and is found particularly advantageous where the precipitating bath contains a high concentration of metallic salts, especially zinc, in concentrations of Accordingly, in the specification and the order of 3% to The invention is also advantageous in spinning other cellulose solutions including cuprammonium and cellulose derivatives such as cellulose acetate as well as other synthetic materials, including copolymers of vinyl chloride and vinyl acetate.
In carrying out the invention a small amount of the surface active material of the order of 0.01 to 0.05 may be dissolved in the spinning solution and the spinning solution is extruded into a precipitating medium. Where a liquid precipitating medium or bath is used, a small amount of the surface active material of the same order may be dissolved in the precipitating medium or may be added to both the spinning solution and the precipitating medium.
The following examples are illustrative of the invention:
1. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% or organic compounds comprising sorbitan monolaurate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethlene content of oxyethylene units per molecule.
2. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a sorbitan monolaurate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 8 oxyethylene units per molecule.
3. A multifilament regenerated cellulose yarnis formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a sorbitan monooleate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
4. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monomyristate having at least 1 hydroxy polyoxyethylene group per molecule and an avdroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
7. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monopalmitate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
8. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% organic compounds comprising a mannitan monostearate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
9. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc'sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising lauryl alcohol in which the hydroxyl group has been replaced by a hydroxy polyoxyethylene group and the average oxyethylene content is 20 oxyethylene units per molecule.
erage oxyethylene content of 20 oxyethylene units per molecule.
5. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monolaurate having at least 1 hydroxy polyoxyethylene group per molecule and an average oxyethylene content of 20 oxyethylene units per molecule.
6. A multifilament regenerated cellulose yarn is formed by extruding a viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising a mannitan monooleate having at least 1 hyl6 10. A multifilament regenerated cellulose yarn is formed by extruding viscose solution through a spinneret into an aqueous sulphuric acid spinning bath containing a high concentration of zinc sulphate of the order of 5% and between 0.02 and 0.03% of organic compounds comprising triricinolein in which at least 1 free hydroxyl group has been replaced by a hydroxy polyoxyethylene group and the average oxyethylene content is 20 oxyethylene units per molecule.
It was found that in carrying out the spinning operation in accordance with the present invention it is necessary to change less than 50% as many spinnerets as where ordinary methods of spinning are followed. Where multifilament yarn is formed the filaments are of uniform crosssection and the yarn is of generally improved quality.
While preferred embodiments of the invention have been shown, it is to be understood that changes and variations may be made without departing from the spirit and scope of the invention as defined by the appended claims.
What I claim is:
1. An aqueous acid medium for precipitating viscose in the form of filaments, films and the like, containing a small amount of a sorbitan monolaurate derivative having at least one polyoxyethylene group, the average oxyethylene content being about 20 oxyethylene units per molecule.
2. An aqueous acid medium for precipitating viscose in the form of filaments, films and the like, containing a small amount of a dissolved ester of a polyhydric alcohol having a hydrophobic group containing at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
3. An aqueous acid medium for precipitating viscose in the form of filaments, films and the like, containing a small amount of a dissolved subcontaining at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, the
oxyethylene content being at least 8 oxyethylene units per molecule.
5. An aqueous medium for precipitating viscose in the form of filaments, films and the like,
containing sulfuric acid and a small amount of a dissolved ester of a polyhydric alcohol having a hydrophobic group containing at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, thefoxyethylene content being at least 8 oxyethylene units per molecule.
6. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid and a small amount of a dissolved substantially stable surface active non-ionogenic polyethylene glycol ether of a partially esterified polyhydric alcohol containing an epoxy group, said esterified polyhydric alcohol containing a hydrophobic radical having a hydrocarbon chain of at least 8 carbon atoms and said ether containing at least 8 oxyethylene units per molecule.
7. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid and a small amount of a dissolved substituted hexitan having a hydrophobic group containing at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
8. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid and a small amount of a substituted sorbitan monolaurate having at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
9. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid and a small amount of a substituted manm'tan monostearate, having at least one polyoxyethylene group, the oxyethylene 1 least 8 oxyethyleneunits per content being at molecule.
10. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid and a small amount of triricinolein in which at least one free hydroxyl group is replaced by a polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
11. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid, a zinc salt and a small amount of a dissolved substantially stable surface active non-ionogenic polyethylene glycol ether of a partially esterified polyhydric alco hol containing an epoxy group, said esterified polyhydric alcohol containing a hydrophobic radical having a hydrocarbon chain of at least 8 carbon atoms and said ether containing at least 8 oxyethylene units per molecule.
12. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid, a zinc salt and a small amount of a dissolved substituted hexitan having a hydrophobic group containing at least 8 carbon atoms in a straight chain and at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
13. An aqueous medium for precipitating viscose in the form of filaments, films and the like,
' containing sulfuric acid, a zinc salt and a small amount of a substituted sorbitan monolaurate having at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
14. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid, a zinc salt and a small amount of a substituted mannitan monostearate having at least one polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
15. An aqueous medium for precipitating viscose in the form of filaments, films and the like, containing sulfuric acid, a zinc salt and a small amount of triricinolein in which at least one free hydroxyl group is replaced by a polyoxyethylene group, the oxyethylene content being at least 8 oxyethylene units per molecule.
BENJAMIN W. COLLINS.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US389325A US2359749A (en) | 1941-04-19 | 1941-04-19 | Manufacture of synthetic yarns and the like |
US396543A US2359750A (en) | 1941-04-19 | 1941-06-04 | Viscose spinning solution |
US751136A US2519227A (en) | 1941-04-19 | 1947-05-28 | Manufacture of yarns and the like |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US389325A US2359749A (en) | 1941-04-19 | 1941-04-19 | Manufacture of synthetic yarns and the like |
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Publication Number | Publication Date |
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US2359749A true US2359749A (en) | 1944-10-10 |
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Application Number | Title | Priority Date | Filing Date |
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US389325A Expired - Lifetime US2359749A (en) | 1941-04-19 | 1941-04-19 | Manufacture of synthetic yarns and the like |
Country Status (1)
Country | Link |
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US (1) | US2359749A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2451558A (en) * | 1944-11-06 | 1948-10-19 | Rayonier Inc | Chemically treated wood pulp and a method of producing a cellulosic product |
US2489310A (en) * | 1942-05-28 | 1949-11-29 | American Viscose Corp | Spinning assistants |
US2519227A (en) * | 1941-04-19 | 1950-08-15 | American Viscose Corp | Manufacture of yarns and the like |
US2970883A (en) * | 1956-01-16 | 1961-02-07 | American Enka Corp | Manufacture of viscose rayon |
US2984541A (en) * | 1959-04-20 | 1961-05-16 | American Viscose Corp | Method of forming all skin viscose rayon |
US3482010A (en) * | 1963-09-30 | 1969-12-02 | Kuraray Co | Process for the production of polyurethane elastic fiber having less adhesivity |
US4098752A (en) * | 1974-07-20 | 1978-07-04 | Idemitsu Kosan Company, Ltd. | Thermoplastic resin composition suitable for extrusion molding |
EP2155817A1 (en) * | 2007-06-11 | 2010-02-24 | Kolon Industries Inc. | Cellulose-based yarn, and method of preparing the same |
-
1941
- 1941-04-19 US US389325A patent/US2359749A/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2519227A (en) * | 1941-04-19 | 1950-08-15 | American Viscose Corp | Manufacture of yarns and the like |
US2489310A (en) * | 1942-05-28 | 1949-11-29 | American Viscose Corp | Spinning assistants |
US2451558A (en) * | 1944-11-06 | 1948-10-19 | Rayonier Inc | Chemically treated wood pulp and a method of producing a cellulosic product |
US2970883A (en) * | 1956-01-16 | 1961-02-07 | American Enka Corp | Manufacture of viscose rayon |
US2984541A (en) * | 1959-04-20 | 1961-05-16 | American Viscose Corp | Method of forming all skin viscose rayon |
US3482010A (en) * | 1963-09-30 | 1969-12-02 | Kuraray Co | Process for the production of polyurethane elastic fiber having less adhesivity |
US4098752A (en) * | 1974-07-20 | 1978-07-04 | Idemitsu Kosan Company, Ltd. | Thermoplastic resin composition suitable for extrusion molding |
EP2155817A1 (en) * | 2007-06-11 | 2010-02-24 | Kolon Industries Inc. | Cellulose-based yarn, and method of preparing the same |
EP2155817A4 (en) * | 2007-06-11 | 2010-06-16 | Kolon Inc | Cellulose-based yarn, and method of preparing the same |
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