US3899614A - Method of producing bundled multifilament yarn - Google Patents

Method of producing bundled multifilament yarn Download PDF

Info

Publication number
US3899614A
US3899614A US450240A US45024074A US3899614A US 3899614 A US3899614 A US 3899614A US 450240 A US450240 A US 450240A US 45024074 A US45024074 A US 45024074A US 3899614 A US3899614 A US 3899614A
Authority
US
United States
Prior art keywords
yarn
random copolymer
ethylene oxide
propylene oxide
agent
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
US450240A
Inventor
Tsuyoshi Okamoto
Yoichi Kawaguchi
Takayuki Kai
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.)
Toyobo Co Ltd
Original Assignee
Toyobo Co Ltd
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
Application filed by Toyobo Co Ltd filed Critical Toyobo Co Ltd
Application granted granted Critical
Publication of US3899614A publication Critical patent/US3899614A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32Polymers modified by chemical after-treatment
    • C08G65/329Polymers modified by chemical after-treatment with organic compounds
    • C08G65/331Polymers modified by chemical after-treatment with organic compounds containing oxygen
    • C08G65/332Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers

Definitions

  • the present invention relates to a method of producing a bundled synthetic fiber multifilament yarn, and more particularly the invention has for its object the production of a bundled multifilament yarn having excellent properties as warps for weaving.
  • a preparatory step is required wherein the warp yarn is first sized and then warped or is sized after warping.
  • the object of such sizing is to give bundling properties and wear resistance to the yarn, to make the adhesion between individual filaments sufficient, and to make the yarn sufficiently resistant to shock, friction and tension during weaving so that the weaving efficiency is improved.
  • pastes which have film-forming ability or adhesiveness. They are, for example, polyvinyl alcohol, esters of polyacrylic acid, sodium polyacrylate, polyacrylic acid, polyacrylamide, etc.
  • the method of the present invention obviates various such difficulties encountered in the conventional sizing step, and moreover simplifies the process by incorporating a sizing step into the yarn producing step.
  • the method of the present invention is characterized in that a random copolymer of ethylene oxide and propylene oxide esterified with rosin is fixed or depositcd singly or together with a lubricating agent, emulsifier, antistatic agent. etc., to an unstretched or stretched synthetic fiber multifllament yarn, and particularly in that the extruded multifilament yarn is treated in the spinning step with an oiling agent containing 5 weight percent of the above-mentioned treating agent based on the total weight of the non-aqueous components,
  • the random copolymers of ethylene oxide and propylene oxide esterified with rosin to be used in the method of the present invention either monoester or diester may be used.
  • the term rosin refers to a natural resin mainly composed of abietic acid, which additionally contains pimaric acid, sabinic acid, etc.
  • the average molecular weight of the random copolymers of ethylene oxide and propylene oxide is preferably within the range of 5,000 to 20,000.
  • the ratio off ethylene oxide to propylene oxide is not required to be particularly limited, but 50 mol percent of ethylene oxide is preferred. When ethylene oxide is less than 50 mol percent, it is difficult to compound such a copolymer into an emulsion, and when ethylene oxide is in excess of 85 mol percent the viscosity of the resulting emulsion becomes considerably high, so that such a copolymer is not desirable.
  • the treating agent of the present invention by reacting a random copolymer of ethylene oxide and propylene oxide with rosin, it is desirable to take the molar ratio of the copolymer and rosin so as to be 1:05 3.0. if rosin is less than 0.5 mol percent, the treated yarn will have seriously inferior hundling properties, and on the other hand when rosin is in excess of 3 mol percent, the obtained yarn will have good bundling properties, but its smoothness becomes remarkably poor and it is liable to generate static electricity.
  • the reaction product besides the above-mentioned random copolymer rosin ester, unreacted random copolymer and rosin are present together. However, the reaction product may be used without particularly separating the unreacted materials. The unreacted rosin may be converted into an alkali metal salt thereof.
  • Yarns treated with such a treating agent of the present invention have a high degree of bundling properties and a high degree of wear resistance as well as a proper degree of smoothness, with the quality of the yarns being further stabilized. Therefore, the yarn obtainable by the present invention are provided with necessary characteristics as warps for weaving so that the yarn may be exempted from a separate sizing step before weaving.
  • the treating agent of the present invention is applied to an unstretched yarn, the treated yarn will have an extremely good stretchability so that entangling of the yarn about rollers or yarn breakage during the production step is few in comparison with the yarn treated with a conventional oiling agent, and fluff of the stretched yaarn becomes markedly reduced.
  • the treating agents of the present invention may be thus applied to the yarn together with an oiling agent in the spinning step or may be applied upon stretching or after stretching.
  • the ratio of the treating agent of the present invention to the general oiling agent be set within the range of 10:0 5:5.
  • the treating agent of the present invention be fixed to the yarn in an amount of more than 0.1 weight percent based on the fiber weight.
  • the total fixed amount of the oiling agent and the treating agent of the present invention is desirable to be small such that it is less than 2 weight percent based on the fiber weight.
  • a fixed amount of less than 2 weight percent based on the fiber is not sufficient for the sized yarn to have an effect as sized yarn. But with the use of the treating agent of the present invention, and a small amount is able to give sufficient bandling properties and wear resistance to the yarn.
  • the multifilament yarn obtainable by the method of the present invention is most suitable as warps for weaving.
  • it is removed from the defects of the conventional sized yarn, such as paste-fall and gum-up.
  • the sizing step can be omitted.
  • the method of the present invention results in good weaving efficiency, few flufff generation during wearing, and improvement in shedding movement.
  • the small fixed amount of the treating agent contributes to the prevention of paste-fall and gum-up and to the quality improvement of the resulting fabrics.
  • EXAMPLE 1 An unstretched multifilament yarn of nylon-6 obtained by melt-spinning, after being unwound from a pirn and prior to entering the stretching zone, was applied with the treating agents Nos. 1 4 shown in Table 1 according to the method of the present invention. Immediately after this'treatment, the yarn was stretched to obtain a nylon-6 multifilament yarn of 70 denier/14 filaments.
  • Each of the treating agents was used as an aqueous emulsion in concentration of 10 which contained 80 of a treating agent of the present invention, 10 of a mineral oil, 5 of a higher fatty acid ester, and 5 71. of a polyoxyethylene nonionic surface active agent, and as an antistatic agent an alkyl phosphate metal salt was added in an amount of 8 based on the non-aqueous components.
  • propylene oxide 25 mol random copolymer (mol. wt. 12,000) rosin diester 2.
  • propylene oxide (25 mol random copolymer (mol. wt. 12,000) rosin monoester 3.
  • Ethylene oxide mol 1.07 wt.
  • the rank B represents a sample having a number of divided filaments from 6 to 9, a divided height from 50 to mm., and a divided width from 5 to 10 mm.
  • the rank C represents a sample having a number of divided filaments more than 10, a divided height more than 100 mm., and a divided width more than 10 mm.
  • a test sample 50 cm. in length, is fixed at one end, and a weight of 50 grams is suspended at the other end. The sample is rubbed at the middle point with a blade traversing horizontally.
  • the rank C is the case where fluff is generated within 5 minutes.
  • the rank B is the case where fluff is generated in 5 10 minutes, and the rank A is the case where no fluff is generated after 10 minutes.
  • the yarn is made to travel over a rubbing rod at a contact angle of 90.
  • the travelling tension of the yarn before passing the rubbing means at a travelling speed of I00 m/min. is fixed constant at 10 grams, and the tension after passing the rubbing means is measured. When this value is less than 1.2, it is ranked as Good," when that of Comparative Example 2 is taken as l.
  • the yarn obtained by the method of the present invention represents a high degree of bundling properties and a high degree of wear resistance as well as a proper degree of smoothness, while the conventional PVA type sizing agent does not show any effect as a bundling agent at the same fixed amount as the treating agent of the present invention, the effect obtained being substantially equal to that obtained in the case of using a spinning oil only.
  • EXAMPLE 2 1n the spinning step of a nylon-6 multifilament yarn of 70 d/14 f., oiling agents each containing 100 weight percent, 70 weight percent, 40 weight percent and 10 weight percent of the ethylene oxide (75 mol %)-propylene oxide (25 mol random copolymer rosin diester were respectively applied to the extruded yarn as an aqueous emulsion in concentration of 15 by means of oiling rollers.
  • the oiling agent components other than the rosin ester were 50 weight percent of a mineral oil, weight percent of a higher fatty acid ester, and 30 weight percent of a polyoxyethylene type nonionic surface active agent, to which, as an antistatic agent, the same one as used in Example 1 was added in an amount of 7 based on the nonaqueous components.
  • the fixed amount was controlled such that the amount of the rosin ester was more than 0.1 weight percent. Too high a total fixed amount generated dirt on drawtwisters. Also, as seen in the above table, too large an amount of the rosin ester in the treating agent lowered the smoothness and increased generation of fluffs. Accordingly, when the treating agent of the present invention is applied together with an oiling agent in the spinning step, it is necessary that the ratio of the treating agent to the oiling agent be adjusted to 5/95 /30, preferably 10/90 50/50.
  • a method of producing bundled multifilament yarn which comprises depositing a rosin ester of a random copolymer of ethylene oxide and propylene oxide on the surface of a synthetic fiber multifilament yarn in an amount of more than 0.1% by weight based on the weight of the yarn, said random copolymer having an average molecular weight of 5,000 to 20,000 and wherein the ratio of ethylene oxide to propylene oxide in the copolymer is 50-85 mol of ethylene oxide to l5-50 mol of propylene oxide.
  • a method of producing bundled mutifilament yarn which comprises melt-spinning the yarn and then treat ing the yarn with an aqueous emulsion of an oily agent in combination with a rosin ester of a random copolymer of ethylene oxide and propylene oxide in an amount of 570% based on the weight of non-aqueous components, said rosin ester being used in an amount of more than 0. l based on the weight of the yarn; and wherein the average molecular weight of the random copolymer is 5000 to 20,000 and the ratio of ethylene oxide to propylene oxide in the copolymer is 50-85 mol of ethylene oxide to 15-50 mol of propylene oxide.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Treatment Of Fibers During Manufacturing Processes (AREA)

Abstract

A method of producing a bundled multifilament yarn is provided herein by fixing a rosin ester of a random copolymer of ethylene oxide and propylene oxide to an unstretched or stretched synthetic fiber multifilament yarn. The rosin ester may be applied to the yarn singly or together with such materials as an emulsifier, antistatic agent or lubricating agent.

Description

United States Patent Okamoto et a1.
[4 1 Aug. 12, 1975 METHOD OF PRODUCING BUNDLED MULTIFILAMENT YARN Inventors: Tsuyoshi Okamoto; Yoichi Kawaguchi; Takayuki Kai, all of Tsuruga, Japan Assignee: Toyo Boseki Kabushiki Kaisha,
Osaka, Japan Filed: Mar. 11, 1974 Appl. No.: 450,240
Foreign Application Priority Data Mar. 10, 1973 Japan 48-28199 US. Cl 427/175; 8/1 15.6; 28/75 R; 264/210 F; 260/2 A; 260/2 XA; 260/24;
Int. C1. C08,] 5/04 Field of Search 117/1395 CO, 139.5 F,
117/138.8 N, 138.8 B, 161 UT, 7; 260/27 R, 24, 2 A, 2 XA; 28/75 R; 264/210 F; 8/1156 [56] References Cited UNITED STATES PATENTS 2,331,840 10/1943 Little 117/1395 CQ 2,343,308 3/1944 Little 117/1395 CQ 2.348.552 5/1944 Little 117/1395 CQ Primary ExaminerWilliam D. Martin Assistant Examiner-Janyce A. Bell Attorney, Agent, or FirmWenderoth, Lind & Ponack 5 7] ABSTRACT 5 Claims, No Drawings METHOD OF PRODUCING BUNDLED MULTIFILAMENT YARN The present invention relates to a method of producing a bundled synthetic fiber multifilament yarn, and more particularly the invention has for its object the production of a bundled multifilament yarn having excellent properties as warps for weaving.
In general, prior to the weaving step for the production of textile fabrics, a preparatory step is required wherein the warp yarn is first sized and then warped or is sized after warping.
The object of such sizing is to give bundling properties and wear resistance to the yarn, to make the adhesion between individual filaments sufficient, and to make the yarn sufficiently resistant to shock, friction and tension during weaving so that the weaving efficiency is improved.
To attain such objects, pastes (or sizing agents) are used which have film-forming ability or adhesiveness. They are, for example, polyvinyl alcohol, esters of polyacrylic acid, sodium polyacrylate, polyacrylic acid, polyacrylamide, etc.
However, sized yarn is greatly influenced by the oiling agent with which the original warp yarn has been treated, and there are various difficulties resulting therefrom.
First, upon immersing warp yarn in a paste liquid, when the compatibility between the oiling agent and the paste liquid is poor, scum is generated which floats on the surface of the paste liquid, while when the compatability is too good, the amount of the oiling agent contained in the paste liquid becomes larger with the passage of time when the liquid is used continuously for a long time, with the result that not only the performance of the paste becomes lowered but also considerable generation of foam is observed. In either case, uneven pick-up of paste is caused and thus the sized yarn becomes of inferior quality,
Secondly, there are often cases in which an oiling agent is a cause of the hindrance of adhesion between the warp yarn and the paste. If an oiling agent which may cause adhesion hindrance is fixed to the warp yarn, even though the sized yarn represents a good appearance, the paste will fall off under the influence of the friction at the heald or reed. Such is generally called paste-fall. The paste made fo fall off becomes sticky by moisture absorption and causes a phenomenon called gum-up. This worsens the shedding movement and seriously impairs the quality of the fabric thus produced. Also, the paste itself is susceptible to the influence of temperature and humidity. Therefore, under circumstances of high temperature and high humidity, the paste will gum up independently of the oiling agent used.
The method of the present invention obviates various such difficulties encountered in the conventional sizing step, and moreover simplifies the process by incorporating a sizing step into the yarn producing step.
The method of the present invention is characterized in that a random copolymer of ethylene oxide and propylene oxide esterified with rosin is fixed or depositcd singly or together with a lubricating agent, emulsifier, antistatic agent. etc., to an unstretched or stretched synthetic fiber multifllament yarn, and particularly in that the extruded multifilament yarn is treated in the spinning step with an oiling agent containing 5 weight percent of the above-mentioned treating agent based on the total weight of the non-aqueous components,
As the random copolymers of ethylene oxide and propylene oxide esterified with rosin to be used in the method of the present invention (hereinafter referred to as the treating agent of the present invention), either monoester or diester may be used. As used herein, the term rosin refers to a natural resin mainly composed of abietic acid, which additionally contains pimaric acid, sabinic acid, etc. The average molecular weight of the random copolymers of ethylene oxide and propylene oxide is preferably within the range of 5,000 to 20,000. In the case of an average molecular weight below 5.000, it is difficult to provide a high degree of bundling properties and a high degree of wear resistance, On the other hand, with an average molecular weight above 20,000, the resulting too high viscosity makes it difficult for the treating agent to fix to the multifilament yarn. The ratio off ethylene oxide to propylene oxide is not required to be particularly limited, but 50 mol percent of ethylene oxide is preferred. When ethylene oxide is less than 50 mol percent, it is difficult to compound such a copolymer into an emulsion, and when ethylene oxide is in excess of 85 mol percent the viscosity of the resulting emulsion becomes considerably high, so that such a copolymer is not desirable.
In this connection, if, in the present invention, the random copolymer of ethylene oxide and propylene oxide is replaced with a block copolymer, the emulsifying power of the rosin ester will become poor and the kinetic friction coefficient of the yarn treated with such ester becomes high, with the smoothness of the yarn becoming bad.
In producing the treating agent of the present invention by reacting a random copolymer of ethylene oxide and propylene oxide with rosin, it is desirable to take the molar ratio of the copolymer and rosin so as to be 1:05 3.0. if rosin is less than 0.5 mol percent, the treated yarn will have seriously inferior hundling properties, and on the other hand when rosin is in excess of 3 mol percent, the obtained yarn will have good bundling properties, but its smoothness becomes remarkably poor and it is liable to generate static electricity. In the reaction product, besides the above-mentioned random copolymer rosin ester, unreacted random copolymer and rosin are present together. However, the reaction product may be used without particularly separating the unreacted materials. The unreacted rosin may be converted into an alkali metal salt thereof.
Yarns treated with such a treating agent of the present invention have a high degree of bundling properties and a high degree of wear resistance as well as a proper degree of smoothness, with the quality of the yarns being further stabilized. Therefore, the yarn obtainable by the present invention are provided with necessary characteristics as warps for weaving so that the yarn may be exempted from a separate sizing step before weaving. When the treating agent of the present invention is applied to an unstretched yarn, the treated yarn will have an extremely good stretchability so that entangling of the yarn about rollers or yarn breakage during the production step is few in comparison with the yarn treated with a conventional oiling agent, and fluff of the stretched yaarn becomes markedly reduced.
The treating agents of the present invention may be thus applied to the yarn together with an oiling agent in the spinning step or may be applied upon stretching or after stretching. However, when they are applied particularly together with an oiling agent in the spinning step, it is necessary that the ratio to other general oiling agents such as lubricating agent, emulsifier, antistatic agent, etc. be suitably adjusted, taking the operation efficiency in spinning and stretching into consideration, so that the treating agent of the present invention occupies 5 70 weight percent, preferably 50 weight percent, of the total weight of the nonaqueous components. Where the treating agent is applied after stretching, since an oiling agent has been already applied in the spinning step, it is preferably that the ratio of the treating agent of the present invention to the general oiling agent be set within the range of 10:0 5:5. In either case where the treating agent of the present invention is applied to an unstretched filament yarn or to stretched filament yarn, it is desirable that the treating agent be fixed to the yarn in an amount of more than 0.1 weight percent based on the fiber weight. Additionally, to prevent paste-fall and gum up and to improve spinnability and stretchability, the total fixed amount of the oiling agent and the treating agent of the present invention is desirable to be small such that it is less than 2 weight percent based on the fiber weight. With an ordinary paste, a fixed amount of less than 2 weight percent based on the fiber is not sufficient for the sized yarn to have an effect as sized yarn. But with the use of the treating agent of the present invention, and a small amount is able to give sufficient bandling properties and wear resistance to the yarn.
The multifilament yarn obtainable by the method of the present invention is most suitable as warps for weaving. In addition to its having bundling properties, wear resistance, anad smoothness comparable to those seen in usual sized yarn, it is removed from the defects of the conventional sized yarn, such as paste-fall and gum-up. Thus, by the method of the present invention, the sizing step can be omitted. In spite of this, the method of the present invention results in good weaving efficiency, few flufff generation during wearing, and improvement in shedding movement. Also, the small fixed amount of the treating agent contributes to the prevention of paste-fall and gum-up and to the quality improvement of the resulting fabrics.
EXAMPLE 1 An unstretched multifilament yarn of nylon-6 obtained by melt-spinning, after being unwound from a pirn and prior to entering the stretching zone, was applied with the treating agents Nos. 1 4 shown in Table 1 according to the method of the present invention. Immediately after this'treatment, the yarn was stretched to obtain a nylon-6 multifilament yarn of 70 denier/14 filaments.
Each of the treating agents was used as an aqueous emulsion in concentration of 10 which contained 80 of a treating agent of the present invention, 10 of a mineral oil, 5 of a higher fatty acid ester, and 5 71. of a polyoxyethylene nonionic surface active agent, and as an antistatic agent an alkyl phosphate metal salt was added in an amount of 8 based on the non-aqueous components.
Table 1 Fixed amount of treating agent No. Treating agent (*nonaqueous components) on the fiber 1. Ethylene oxide mol 1.10 wt.
propylene oxide (25 mol random copolymer (mol. wt. 12,000) rosin diester 2. Ethylene oxide (75 mol 1.12 wt.
propylene oxide (25 mol random copolymer (mol. wt. 12,000) rosin monoester 3. Ethylene oxide mol 1.07 wt.
propylene oxide 15 mol random copolymer (mol. wt. 12,000) rosin diester Including a 0.6 wt. 7r fixcd amount of a spinning oil.
Characteristic properties of the yarns thus obtained are shown in Table 2 together with those of Comparative Example 1 wherein the yarn was treated with a PVA type paste in place of the treating agent of the present invention (*fixed amount on the fiber 1.12 wt. and Comparative Example 2 wherein only a Bundling properties One end of a test sample, 30 cm. in length, is fixed and a weight of 25 grams is suspended at the other end. The sample is cut with a sharp knife at a point of 20 cm. from the fixed end. The number of divided filaments, the height and width of the divided portion are measured and ranked in A, B, and C. The rank A represents a sample having a number of divided filaments less than 5, a divided height less than 50 mm., and a divided width less than 5 mm. The rank B represents a sample having a number of divided filaments from 6 to 9, a divided height from 50 to mm., and a divided width from 5 to 10 mm., and the rank C represents a sample having a number of divided filaments more than 10, a divided height more than 100 mm., and a divided width more than 10 mm.
Wear resistance A test sample, 50 cm. in length, is fixed at one end, and a weight of 50 grams is suspended at the other end. The sample is rubbed at the middle point with a blade traversing horizontally. The rank C is the case where fluff is generated within 5 minutes. The rank B is the case where fluff is generated in 5 10 minutes, and the rank A is the case where no fluff is generated after 10 minutes.
Table 3 Fixed Rosin amount of Bundl- Fluffs Weaving ester treating *Strctching Wear pcr efiicontent agent Spinnability propcrresis- Smoothmillion cicncy No. (wt. 9?) (wt. '71) ability tics tancc ncss meters (71) 5 I00 0.43 Dirt 75 A A Bad 2.0 90
generated on guides 6 70 0.52 Good 95 A A Good 0.33 95 7 40 075 Good 97 A A Good 0.15 97 8 10 l .60 Good 98 A A Good 0.06 97 'Slrctchahility: Percentage perfect full pirns to the total irns operated.
Smoothness The yarn is made to travel over a rubbing rod at a contact angle of 90. The travelling tension of the yarn before passing the rubbing means at a travelling speed of I00 m/min. is fixed constant at 10 grams, and the tension after passing the rubbing means is measured. When this value is less than 1.2, it is ranked as Good," when that of Comparative Example 2 is taken as l.
Weaving efficiency This is expressed by the percentage operation of the weaving machine.
As apparent from Table 2, the yarn obtained by the method of the present invention represents a high degree of bundling properties and a high degree of wear resistance as well as a proper degree of smoothness, while the conventional PVA type sizing agent does not show any effect as a bundling agent at the same fixed amount as the treating agent of the present invention, the effect obtained being substantially equal to that obtained in the case of using a spinning oil only.
EXAMPLE 2 1n the spinning step of a nylon-6 multifilament yarn of 70 d/14 f., oiling agents each containing 100 weight percent, 70 weight percent, 40 weight percent and 10 weight percent of the ethylene oxide (75 mol %)-propylene oxide (25 mol random copolymer rosin diester were respectively applied to the extruded yarn as an aqueous emulsion in concentration of 15 by means of oiling rollers. The oiling agent components other than the rosin ester were 50 weight percent of a mineral oil, weight percent of a higher fatty acid ester, and 30 weight percent of a polyoxyethylene type nonionic surface active agent, to which, as an antistatic agent, the same one as used in Example 1 was added in an amount of 7 based on the nonaqueous components.
The spinnability and stretchability of the thus obtained yarn are shown in Table 3 together with other characteristic properties.
The fixed amount was controlled such that the amount of the rosin ester was more than 0.1 weight percent. Too high a total fixed amount generated dirt on drawtwisters. Also, as seen in the above table, too large an amount of the rosin ester in the treating agent lowered the smoothness and increased generation of fluffs. Accordingly, when the treating agent of the present invention is applied together with an oiling agent in the spinning step, it is necessary that the ratio of the treating agent to the oiling agent be adjusted to 5/95 /30, preferably 10/90 50/50.
What we claim is:
1. A method of producing bundled multifilament yarn which comprises depositing a rosin ester of a random copolymer of ethylene oxide and propylene oxide on the surface of a synthetic fiber multifilament yarn in an amount of more than 0.1% by weight based on the weight of the yarn, said random copolymer having an average molecular weight of 5,000 to 20,000 and wherein the ratio of ethylene oxide to propylene oxide in the copolymer is 50-85 mol of ethylene oxide to l5-50 mol of propylene oxide.
2. A method according to claim 1, wherein a lubricating agent, an antistatic agent or an emulsifier is codeposited on the synthetic fiber multifilament yarn along with the rosin ester of the random copolymer.
3. A method according to claim 1, wherein the rosin ester of the random copolymer is deposited on the synthetic fiber multifilament yarn while in an unstretched state.
4. A method according to claim 1, wherein the rosin ester of the random copolymer is deposited on a stretched synthetic fiber multifilament yarn.
5. A method of producing bundled mutifilament yarn which comprises melt-spinning the yarn and then treat ing the yarn with an aqueous emulsion of an oily agent in combination with a rosin ester of a random copolymer of ethylene oxide and propylene oxide in an amount of 570% based on the weight of non-aqueous components, said rosin ester being used in an amount of more than 0. l based on the weight of the yarn; and wherein the average molecular weight of the random copolymer is 5000 to 20,000 and the ratio of ethylene oxide to propylene oxide in the copolymer is 50-85 mol of ethylene oxide to 15-50 mol of propylene oxide.

Claims (5)

1. A METHOD OF PRODUCING BUNDLED MULTIFILAMENT YARN WHECH COMPRISES DEPOSITING A ROSIN ESTER OF A RANDOM COPOLYMER OF ETHYLENE OXIDE AND PROPYLENE OXIDE ON THE SURFACE OF A SYNTHETIC FIBER MULTIFILAMENT YARN IN AN AMOUNT OF MORE THAN 0.1% BY EIGHT BASED ON THE WEIHT OF THE YARN, SAID RANDOM COPOLYMER HAVING AN VERAGE MOLECULAR WEIGHT OF5,000 TO 20,000 AND WHEREIN THE RATIO OF ETHYLENE OXIDE TO PROPYLENE OXIDE IN THE COPOLYMER IS 50-85 MOL % OF ETHYLENE OXIDE TO 15-50 MOL % OF PROPYLENE OXIDE.
2. A method according to claim 1, wherein a lubricating agent, an antistatic agent or an emulsifier is co-deposited on the synthetic fiber multifilament yarn along with the rosin ester of the random copolymer.
3. A method according to claim 1, wherein the rosin ester of the random copolymer is deposited on the synthetic fiber multifilament yarn while in an unstretched state.
4. A method according to claim 1, wherein the rosin ester of the random copolymer is deposited on a stretched synthetic fiber multifilament yarn.
5. A method of producing bundled mutifilament yarn which comprises melt-spinning the yarn and then treating the yarn with an aqueous emulsion of an oily agent in combination with a rosin ester of a random copolymer of ethylene oxide and propylene oxide in an amount of 5-70% based on the weight of non-aqueous components, said rosin ester being used in an amount of more than 0.1% based on the weight of the yarn; and wherein the average molecular weight of the random copolymer is 5000 to 20,000 and the ratio of ethylene oxide to propylene oxide in the copolymer is 50-85 mol % of ethylene oxide to 15-50 mol % of propylene oxide.
US450240A 1973-03-10 1974-03-11 Method of producing bundled multifilament yarn Expired - Lifetime US3899614A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2819973A JPS5335640B2 (en) 1973-03-10 1973-03-10

Publications (1)

Publication Number Publication Date
US3899614A true US3899614A (en) 1975-08-12

Family

ID=12241989

Family Applications (1)

Application Number Title Priority Date Filing Date
US450240A Expired - Lifetime US3899614A (en) 1973-03-10 1974-03-11 Method of producing bundled multifilament yarn

Country Status (3)

Country Link
US (1) US3899614A (en)
JP (1) JPS5335640B2 (en)
GB (1) GB1430879A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4442249A (en) * 1982-10-07 1984-04-10 Fiber Industries, Inc. Partially oriented polyester yarn finish
US4516394A (en) * 1982-09-07 1985-05-14 Celanese Corporation Yarn package for spiralers
US4607481A (en) * 1982-09-07 1986-08-26 Celanese Corporation Process for spiral wrapping reinforcement filaments
US6123982A (en) * 1998-09-01 2000-09-26 Colgate-Palmolive Company Dental floss
US20040161604A1 (en) * 2003-02-18 2004-08-19 Milliken & Company Wax-free lubricant for use in sizing yarns, methods using same and fabrics produced therefrom
US20040234758A1 (en) * 2003-05-20 2004-11-25 Demott Roy P. Lubricant and soil release finish for textured yarns, methods using same and fabrics produced therefrom

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5237896A (en) * 1975-09-17 1977-03-24 Toray Industries Multiifilament yarn for water jet loom and fabric weaving method
JPS5862698U (en) * 1981-10-21 1983-04-27 ウエン−フア・ユ− Ash-absorbing electric blackboard wiper
TW202124664A (en) * 2019-10-17 2021-07-01 日商荒川化學工業股份有限公司 Water-dispersed composition for fiber processing fiber products that do not impair the functions of fiber processing agents such as water repellency, durable water repellency, and antifouling properties, and are excellent in slippage, texture, and whitening resistance

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2331840A (en) * 1940-10-12 1943-10-12 Hercules Powder Co Ltd Textile fiber and method of producing
US2343308A (en) * 1941-05-02 1944-03-07 Hercules Powder Co Ltd Textile fiber and method of producing
US2348552A (en) * 1941-03-27 1944-05-09 Hercules Powder Co Ltd Textile fiber and method of producing

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS491887A (en) * 1972-04-25 1974-01-09

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2331840A (en) * 1940-10-12 1943-10-12 Hercules Powder Co Ltd Textile fiber and method of producing
US2348552A (en) * 1941-03-27 1944-05-09 Hercules Powder Co Ltd Textile fiber and method of producing
US2343308A (en) * 1941-05-02 1944-03-07 Hercules Powder Co Ltd Textile fiber and method of producing

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4516394A (en) * 1982-09-07 1985-05-14 Celanese Corporation Yarn package for spiralers
US4607481A (en) * 1982-09-07 1986-08-26 Celanese Corporation Process for spiral wrapping reinforcement filaments
US4442249A (en) * 1982-10-07 1984-04-10 Fiber Industries, Inc. Partially oriented polyester yarn finish
US6123982A (en) * 1998-09-01 2000-09-26 Colgate-Palmolive Company Dental floss
US20040161604A1 (en) * 2003-02-18 2004-08-19 Milliken & Company Wax-free lubricant for use in sizing yarns, methods using same and fabrics produced therefrom
WO2004074562A2 (en) * 2003-02-18 2004-09-02 Milliken & Company Wax-free lubricant for use in sizing yarns, methods using same and fabrics produced therefrom
WO2004074562A3 (en) * 2003-02-18 2005-12-15 Milliken & Co Wax-free lubricant for use in sizing yarns, methods using same and fabrics produced therefrom
US7144600B2 (en) 2003-02-18 2006-12-05 Milliken & Company Wax-free lubricant for use in sizing yarns, methods using same and fabrics produced therefrom
US20040234758A1 (en) * 2003-05-20 2004-11-25 Demott Roy P. Lubricant and soil release finish for textured yarns, methods using same and fabrics produced therefrom
US7579047B2 (en) 2003-05-20 2009-08-25 Milliken & Company Lubricant and soil release finish for textured yarns, methods using same and fabrics produced therefrom

Also Published As

Publication number Publication date
JPS5335640B2 (en) 1978-09-28
GB1430879A (en) 1976-04-07
JPS49116317A (en) 1974-11-07

Similar Documents

Publication Publication Date Title
US3563021A (en) Interlaced yarn and method of making same
US3899614A (en) Method of producing bundled multifilament yarn
US4222922A (en) Warp size for filament yarn consisting essentially of polyvinyl alcohol having a degree of hydrolysis of 88-100%, quaternary ammonium surfactant and plasticizer
US2438968A (en) Production of textile filaments, fibers, and yarns
JP3378181B2 (en) Polyester monofilament for screen gauze
US2278902A (en) Yarn sizing process
US2385110A (en) Treatment of textile materials
US4844709A (en) A textile sizing process using a waxless polyvinyl alcohol size composition
JPH02269878A (en) Production of false twist textured polyester yarn
US4845140A (en) Waxless polyvinyl alcohol size composition
US3855776A (en) Synthetic thermoplastic multifilament yarns
US3084070A (en) Warp size comprising high molecular weight styrene/maleic anhydride copolymer
US3959534A (en) Process for producing fibers
US3711323A (en) Textile size
US3455771A (en) Method for binding the filaments in an untwisted synthetic filament yarn
JPH0340873A (en) Oil composition for warp of non-twist and non-size woven fabric and high-speed fabrication using same oil composition
CA1132285A (en) Polyvinyl alcohol warp size for filament yarn
JP3525603B2 (en) Water jet loom non-twisted non-glue weft for weaving and method for producing the same
JPS5926547A (en) Polyamide filament flat fabric
US2797709A (en) Non-slash weaving
JPS6021934A (en) Untwisted non-sized filament yarn
JP2983397B2 (en) Synthetic fiber for seat belt
JPS6030369B2 (en) Method for manufacturing yarn for water jet trum weaving
JPH03249277A (en) Method for drawing and warping polyester-based synthetic fiber
JPS61146872A (en) Weft yarn treating agent for air jet loom