US2990604A - Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns - Google Patents

Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns Download PDF

Info

Publication number
US2990604A
US2990604A US670383A US67038357A US2990604A US 2990604 A US2990604 A US 2990604A US 670383 A US670383 A US 670383A US 67038357 A US67038357 A US 67038357A US 2990604 A US2990604 A US 2990604A
Authority
US
United States
Prior art keywords
filaments
lubricating
yarns
weight
lubricating composition
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
US670383A
Inventor
Maccormack Kenneth Earnshaw
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Application granted granted Critical
Publication of US2990604A publication Critical patent/US2990604A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/62Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
    • 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
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/104Aromatic fractions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/106Naphthenic fractions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/108Residual fractions, e.g. bright stocks
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/042Metal salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/46Textile oils
    • 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
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions

Definitions

  • the known lubricating compositions comprise emulsions of a polymer or a mineral oil in Water, with suitable additives. These lubricating compositions although satisfactory for the subsequent textile operations at room temperature, give rise to a cumulative solid deposit when the filaments and yarns make sliding contact with hot metal surfaces, during prolonged running. Frequent cleaning of the hot metal surfaces becomes necessary, to prevent sticking and breakage of the moving filaments. Moreover wear of the hot metal surfaces takes place particularly during treatment of high tenacity filaments, such as polyethylene terephthalate filaments. Furthermore considerable care is necessary in compounding these lubricating compositions in order to obtain a relatively stable emulsion and to prevent separation during stoppages and during storage, when no agitation of the emulsion takes place.
  • I in a process for treating filaments and yarns by heating in sliding contact with a hot metal surface in the presence of a lubricating composition, I provide the improvement which comprises using as lubricating composition an aqueous solution containing up to 20% by weight of a polyethylene oxide condensate and up to by weight of an antistatic agent.
  • the solution Preferably the solution also contains up to 1% by weight of a boundary lubricant.
  • the improvement of the treatment of my invention becomes most apparent when the filaments or yarn are making sliding contact with a metal surface heated above 140 C. particularly at low transverse pressures, e.g. when the filaments make tangential contact with a substantially flat metal surface such as a hot plate. There is no formation of solid deposits from my lubricating compositions under these conditions, which bring about a considerable amount of deposition from the lubricants'of the prior art.
  • high transverse pressures e.g. when the filaments or yarn are drawn round a hot pin, which in the case of polyethylene terephthalate filaments is heated to above 80 C., wear of the metal is greatly reduced using the composition of my invention as opposed to those of the prior art.
  • the preferred polyethylene oxide condensates are the polyethylene glycols which are liquids at room temperature. From the polyethylene glycols those having an average molecular weight in the range 200-600 are particularly suitable. Solid polyethylene glycols of average molecular weight higher than '600 may be used if desired, but they must be soluble in the lubricating composition.
  • the antistatic agents used in quantities of less than 10% by weight, must also be water soluble, and sufficiently volatile at the processing temperatures to prevent the formation of deposits during prolonged Any known agents may be used e.g. Lubrol W (registered trademark).
  • boundary lubricant should be soluble in the lubricating composition. When an antistatic agent is used this may be selected to assist the dissolving of the boundary lubricant. I have found the presence of Lubrol W (registered trademark) to assist the dissolving of sodium stearate.
  • Lubrol W registered trademark
  • the slight tendency of some boundary lubricants e.g. fatty acid compounds, such as sodium steal-ate, to precipitate may be overcome by the inclusion of an alkali, such as sodium hydroxide, to raise the pH of the solution to between 8 and 9.
  • the lubricating compositions may be applied to the filaments at any stage of manufacture prior to making contact with the hot metal surface. Conveniently this may be done, e.g. in a melt spinning process after the filaments have solidified, as the filaments come from the spinneret.
  • the amount of any particular lubricating composition picked up by the filaments using a given means for application will depend on their denier and the yarn structure. Suitable amounts are 5% to 20%.
  • the lubricating composition may be applied by any means known in the art in such quantities that all the filaments are covered by the lubricating composition. When the major proportion of the water evaporates from the lubricating com.- position, the remaining components form an evenly distributed film on the filametn surface.
  • a second composition is prepared consisting of:
  • Another lubricating composition is prepared consisting of:
  • Another lubricating composition is prepared from:
  • Lubricant E A lubricating composition similar to Example D is prepared using: Parts Polyethylene glycol 400 5 Antistatic agent Lubrol W 0.5 Sodium stearate-boundary lubricant 0.025 Water to make up 100 parts.
  • Lubricant F A similar lubricating composition to Example E is prepared using:
  • the lubricating compositions A to F are each applied to a separate large batch of solidified polyethylene terephthalate filaments as they come from the spinneret before being wound up as filament yarn, and prior to a drawing process.
  • the amount of the non-aqueous components of the lubricating composition retained on the filaments is from 0.5% to 1% by wei'gth of the yarn.
  • the batches of polyethylene terephthalate filament yarns are subjected to a drawing process, at speeds of at least 150 metres per minute during 14 days continuous drawing. Satisfactory drawing conditions at draw ratios up to 4.5 times are obtained using a hot pin at 85 C., followed by a hot plate at 175 C. Excellent filament yarns during 14 days continuous drawing are obtained and no build up of deposits and little wear on any of the hot chromium plated pins and plates is observed.
  • polyethylene terephthalate filaments are drawn under the same conditions as described but in the presence of an aqueous lubricating emulsion comprising a mineral oil, a Turkey red oil, triethanolamine and diethylene glycol, a brown cumulative'solid deposit is formed on the plates within 12 hours drawing, and the plates require cleaning after 48 hours drawing. If the deposits are not removed frequent filament breaks occur and the uniformity of the drawn filaments is impaired.
  • an aqueous lubricating emulsion comprising a mineral oil, a Turkey red oil, triethanolamine and diethylene glycol
  • EXAMPLE 2 A lubricating composition as described in Example 1 is used in a process for making potentially crimped continuous polyethylene terephthalate filaments by heating the moving continuous filaments while passing over a narrow heated metal surface so that the filaments are heated non-uniformly on one side only continuously along their length while under a tension to give a stretch to the filaments of not more than 10%, as described in the above-mentioned copending application Serial No. 625,291.
  • the hot metal surface is heated to a temperature above 270 up to 900 C. Prolonged continuous running is obtained using the above lubricating composition and no build up on the hot metal surface occurs.
  • Running speeds of at least 500 metres per minute are possible, when using the above lubricant, in quantities such that at least 0.3% of non-aqueous components of the lubricating composition is deposited on the filaments.
  • the potentially crimped filaments are wound up and subjected to a heat relaxation treatment which develops the crimp.
  • Example 1 By comparison if instead of the lubricating composition of Example 1 one of the known lubricating compositions is used, comprising an aqueous emulsion of a mineral oil, Turkey red oil, triethanolamine oleate and diethylene gly- C01 in water, a deposit is formed on the hot metal surface within 3 hours, which has to be removed. Operation has to be stopped and the hot metal surface allowed to cool before the deposit is removed. In spite of this cleaning, the number of filament breaks which cause laps, is increased 30 times and the number of complete breaks in the threadline, affecting all filaments simultaneously, is increased 20 times.
  • a process for thermally treating and lubricating polyethylene terephthalate filaments and yarns when making sliding contact with stationary metal surfaces heated to above C. which comprises applying to said filaments an aqueous lubricating composition which is a solution and which consists essentially of 220% by weight of a polyethylene glycol having an average molecular weight between 200 and 600 and which by itself is a liquid at room temperature, and up to 10% by weight of an antistatic agent, so that the amount of the non-aqueous component of said solution on the filaments is at least 0.2% by weight of the filaments, and thereafter slidably contacting the filaments with said metal surface at a temperature above 140 C.
  • an aqueous lubricating composition which is a solution and which consists essentially of 220% by weight of a polyethylene glycol having an average molecular weight between 200 and 600 and which by itself is a liquid at room temperature, and up to 10% by weight of an antistatic agent, so that the amount of the non-aqueous component of said solution on the filaments

Landscapes

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

Description

United States Patent" f 2,990,604 PROCESS OF THERMALLY TREATING AND LUBRI'CATING POLYETHYLENE TEREPH- THALATE FILAMENTS AND YARNS Kenneth Earnshaw MacConnack, Harrogate, England, assignor to Imperial Chemical Industries Limited, Millbank, London, England, a corporation of Great Britain No Drawing. Filed July 8, 1957, Ser. No. 670,383 Claims priority, application Great Britain July 18, 1956 5 Claims. (Cl. 28-72) This invention relates to an improved process for treating filaments and yarns which are heated in sliding contact With a hot metal surface and lubricating compositions for use in such processes.
In the manufacture of artificial filaments and yarns it is often necessary to heat the filaments or yarns whilst making sliding contact with a hot metal surface, e.g. during drawing, relaxing, crimping and heat setting. During subsequent textile operations such as winding, doubling, knitting and weaving the filaments and yarns are subjected to considerable friction whilst passing over various ceramic, metal and similar guides. To minimise friction and to facilitate these textile operations the filaments and yarns are provided with a lubricating composition during manufacture.
The known lubricating compositions comprise emulsions of a polymer or a mineral oil in Water, with suitable additives. These lubricating compositions although satisfactory for the subsequent textile operations at room temperature, give rise to a cumulative solid deposit when the filaments and yarns make sliding contact with hot metal surfaces, during prolonged running. Frequent cleaning of the hot metal surfaces becomes necessary, to prevent sticking and breakage of the moving filaments. Moreover wear of the hot metal surfaces takes place particularly during treatment of high tenacity filaments, such as polyethylene terephthalate filaments. Furthermore considerable care is necessary in compounding these lubricating compositions in order to obtain a relatively stable emulsion and to prevent separation during stoppages and during storage, when no agitation of the emulsion takes place.
According to my invention, in a process for treating filaments and yarns by heating in sliding contact with a hot metal surface in the presence of a lubricating composition, I provide the improvement which comprises using as lubricating composition an aqueous solution containing up to 20% by weight of a polyethylene oxide condensate and up to by weight of an antistatic agent. Preferably the solution also contains up to 1% by weight of a boundary lubricant.
The improvement of the treatment of my invention becomes most apparent when the filaments or yarn are making sliding contact with a metal surface heated above 140 C. particularly at low transverse pressures, e.g. when the filaments make tangential contact with a substantially flat metal surface such as a hot plate. There is no formation of solid deposits from my lubricating compositions under these conditions, which bring about a considerable amount of deposition from the lubricants'of the prior art. At high transverse pressures, e.g. when the filaments or yarn are drawn round a hot pin, which in the case of polyethylene terephthalate filaments is heated to above 80 C., wear of the metal is greatly reduced using the composition of my invention as opposed to those of the prior art.
The preferred polyethylene oxide condensates are the polyethylene glycols which are liquids at room temperature. From the polyethylene glycols those having an average molecular weight in the range 200-600 are particularly suitable. Solid polyethylene glycols of average molecular weight higher than '600 may be used if desired, but they must be soluble in the lubricating composition.
The antistatic agents, used in quantities of less than 10% by weight, must also be water soluble, and sufficiently volatile at the processing temperatures to prevent the formation of deposits during prolonged Any known agents may be used e.g. Lubrol W (registered trademark).
The inclusion of less than 1% of a material which acts as a boundary lubricant between the yarn and the hot metal surface, such as sodium stearate, assists smooth morning and reduces wear of the hot metal surface with which the filaments make contact. It is essential that the boundary lubricant should be soluble in the lubricating composition. When an antistatic agent is used this may be selected to assist the dissolving of the boundary lubricant. I have found the presence of Lubrol W (registered trademark) to assist the dissolving of sodium stearate. The slight tendency of some boundary lubricants e.g. fatty acid compounds, such as sodium steal-ate, to precipitate may be overcome by the inclusion of an alkali, such as sodium hydroxide, to raise the pH of the solution to between 8 and 9.
The prevention of the build up of solid deposits from the lubricating composition during prolonged running at high temperatures is assisted if the components do'not decompose on the hot metal surface. However, in some cases, e.g. in the special crimping process described in Speakman and MacLeod copending application, Serial No. 625,291, filed November 30, 1956, now Patent No. 2,974,391, it is necessary to use a metal surface at such high temperatures, i.e. above 270 C., that decomposition of the organic components of the lubricating composition cannot be prevented. 'The decomposition products in this case should be sufficiently volatile so that they do not form a cumulative solid deposit on the metal surface.
The lubricating compositions may be applied to the filaments at any stage of manufacture prior to making contact with the hot metal surface. Conveniently this may be done, e.g. in a melt spinning process after the filaments have solidified, as the filaments come from the spinneret. The amount of any particular lubricating composition picked up by the filaments using a given means for application will depend on their denier and the yarn structure. Suitable amounts are 5% to 20%. The lubricating composition may be applied by any means known in the art in such quantities that all the filaments are covered by the lubricating composition. When the major proportion of the water evaporates from the lubricating com.- position, the remaining components form an evenly distributed film on the filametn surface. It will be appreciated that small quantities of water are retained by any hygroscopic components of the lubricating composition. The amounts of the non-aqueous components of the lubricating composition remaining on the filaments should preferably be at least 0.2% on the weight of the filaments and the quantities of lubricating composition applied should therefore be adjusted accordingly.
The following examples, in which all parts and per= centages are by weight, illustrate but do not limit my invention.
thylene glycol of an average molecular erg t300 Parts Lubricant B A second composition is prepared consisting of:
Parts Polyethylene glycol 200 2 Antistatic agent Zelec NE (registered trademark) 3 Water 95 Lubricant C Another lubricating composition is prepared consisting of:
Parts Polyethylene glycol 200 2 Antistatic agent Heatex (registered trademark) 3 Water 95 Lubricant D Another lubricating composition is prepared from:
. Parts Polyethylene glycol 200 5 Antistatic agent Lubrol W 0.5 Sodium stearate-boundary lubricant 0.02 Water to make up 100 parts.
Lubricant E A lubricating composition similar to Example D is prepared using: Parts Polyethylene glycol 400 5 Antistatic agent Lubrol W 0.5 Sodium stearate-boundary lubricant 0.025 Water to make up 100 parts.
Lubricant F A similar lubricating composition to Example E is prepared using:
' Parts Polyethylene glycol 300 5 Antistatic agent Lubrol W 2 Sodium stearate-boundary lubricant 0.2
Water to make up 100 parts.
The lubricating compositions A to F are each applied to a separate large batch of solidified polyethylene terephthalate filaments as they come from the spinneret before being wound up as filament yarn, and prior to a drawing process. The amount of the non-aqueous components of the lubricating composition retained on the filaments is from 0.5% to 1% by wei'gth of the yarn. The batches of polyethylene terephthalate filament yarns are subjected to a drawing process, at speeds of at least 150 metres per minute during 14 days continuous drawing. Satisfactory drawing conditions at draw ratios up to 4.5 times are obtained using a hot pin at 85 C., followed by a hot plate at 175 C. Excellent filament yarns during 14 days continuous drawing are obtained and no build up of deposits and little wear on any of the hot chromium plated pins and plates is observed.
By comparison if the polyethylene terephthalate filaments are drawn under the same conditions as described but in the presence of an aqueous lubricating emulsion comprising a mineral oil, a Turkey red oil, triethanolamine and diethylene glycol, a brown cumulative'solid deposit is formed on the plates within 12 hours drawing, and the plates require cleaning after 48 hours drawing. If the deposits are not removed frequent filament breaks occur and the uniformity of the drawn filaments is impaired.
Other improvements were observed in this comparative trial and particularly the following were noted:
(a) A more even application of the lubricating compositions A to F is obtained than can be obtained with the lubricating emulsion of the comparison. The percentage coefficient of variation in the amount of finish applied is reduced to one third, compared with the lubrieating emulsion.
(b) No objectionable fuming occurs when the yarns are passed over the hot metal pins and plates, whereas the lubricating emulsion gives rise to considerable and objectionable fuming.
(0) With the lubricating composition F, for example, wear of the metal surfaces is considerably less, than with the lubricating emulsion.
EXAMPLE 2 A lubricating composition as described in Example 1 is used in a process for making potentially crimped continuous polyethylene terephthalate filaments by heating the moving continuous filaments while passing over a narrow heated metal surface so that the filaments are heated non-uniformly on one side only continuously along their length while under a tension to give a stretch to the filaments of not more than 10%, as described in the above-mentioned copending application Serial No. 625,291. The hot metal surface is heated to a temperature above 270 up to 900 C. Prolonged continuous running is obtained using the above lubricating composition and no build up on the hot metal surface occurs. Running speeds of at least 500 metres per minute are possible, when using the above lubricant, in quantities such that at least 0.3% of non-aqueous components of the lubricating composition is deposited on the filaments. The potentially crimped filaments are wound up and subjected to a heat relaxation treatment which develops the crimp.
By comparison if instead of the lubricating composition of Example 1 one of the known lubricating compositions is used, comprising an aqueous emulsion of a mineral oil, Turkey red oil, triethanolamine oleate and diethylene gly- C01 in water, a deposit is formed on the hot metal surface within 3 hours, which has to be removed. Operation has to be stopped and the hot metal surface allowed to cool before the deposit is removed. In spite of this cleaning, the number of filament breaks which cause laps, is increased 30 times and the number of complete breaks in the threadline, affecting all filaments simultaneously, is increased 20 times.
What I claim is:
1. A process for thermally treating and lubricating polyethylene terephthalate filaments and yarns when making sliding contact with stationary metal surfaces heated to above C., which comprises applying to said filaments an aqueous lubricating composition which is a solution and which consists essentially of 220% by weight of a polyethylene glycol having an average molecular weight between 200 and 600 and which by itself is a liquid at room temperature, and up to 10% by weight of an antistatic agent, so that the amount of the non-aqueous component of said solution on the filaments is at least 0.2% by weight of the filaments, and thereafter slidably contacting the filaments with said metal surface at a temperature above 140 C.
2. The process of claim 1, wherein said amount of said non-aqueous component on the filament is from about 0.5% to about 1% by weight of the filaments.
3. A process according to claim 1, wherein the aqueous solution also contains up to 1% by weight of a boundary lubricant.
4. A process according to claim 3, wherein sodium stearate is present in the aqueous solution 'as a boundary lubricant.
5. A process according to claim 3, wherein the aqueous solution contains a boundary lubrication and the pH of the solution is raised to between 8 and 9 by the inclusion of sodium hydroxide.
References Cited in the file of this patent UNITED STATES PATENTS 6 Wilkes et a1. Aug. 7, 1945 Myers Jan. 29, 1946 Sitzler et a1 Feb. 5, 1946 Rossin et a1 Aug. 10, 1954 Schofield Apr. 17, 1956 Kolb Aug. 14, 1956 Welles et a1 Oct. 8, 1957 Asten Dec. 23, 1958 Mooberry Jan. 12, 1960 Coplan et a1 Feb. 23, 1960 OTHER REFERENCES Tech. Review, vol. 55, No. 8, pages 425-427, June 1953, Electricity in the Textile Industry. Copy in 57-157AS-

Claims (1)

1. A PROCESS FOR THERMALLY TREATING AND LUBRICATING POLYETHYLENE TEREPHTHALATE FILAMENTS AND YARNS WHEN MAKING SLIDING CONTACT WITH STATIONARY METAL SURFACES HEATED TO ABOVE 140*C., WHICH COMPRISES APPLYING TO SAID FILAMENTS AN AQUEOUS LUBRICATING COMPOSITION WHICH IS A SOLUTION AND WHICH CONSISTS ESSENTIALLY OF 2-20% BY WEIGHT OF A POLYETHYLENE GLYCOL HAVING AN AVERAGE MOLECULAR WEIGHT BETWEEN 200 AND 600 AND WHICH BY ITSELF IS A LIQUID AT ROOM TEMPERATURE, AND UP TO 10% BY WEIGHT OF AN ANTISTATIC AGENT, SO THAT THE AMOUNT OF THE NON-AQUEOUS COMPONENT OF SAID SOLUTION ON THE FILAMENTS IS AT LEAST 0.2% BY WEIGHT OF THE FILAMENTS, AND THEREAFTER SLIDABLY CONTACTING THE FILAMENTS WITH SAID METAL SURFACE AT A TEMPERATURE ABOVE 140*C.
US670383A 1956-07-18 1957-07-08 Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns Expired - Lifetime US2990604A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB22224/56A GB833450A (en) 1956-07-18 1956-07-18 Treating filaments and fibres

Publications (1)

Publication Number Publication Date
US2990604A true US2990604A (en) 1961-07-04

Family

ID=10175932

Family Applications (1)

Application Number Title Priority Date Filing Date
US670383A Expired - Lifetime US2990604A (en) 1956-07-18 1957-07-08 Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns

Country Status (7)

Country Link
US (1) US2990604A (en)
BE (1) BE559327A (en)
CH (1) CH377042A (en)
DE (1) DE1105108B (en)
ES (1) ES236495A1 (en)
FR (1) FR1179107A (en)
GB (1) GB833450A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3113369A (en) * 1960-05-02 1963-12-10 Monsanto Chemicals Yarn manufacture and products obtained thereby
US3140957A (en) * 1960-02-23 1964-07-14 Kurashiki Rayon Co Heat treatment of fibers
US4356139A (en) * 1980-12-12 1982-10-26 Southwire Company Method for lubricating cable in a dry curing system

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1072484A (en) * 1963-04-11 1967-06-14 Ici Ltd Improvements in the treatment of polyester fibrous materials and films

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1171195A (en) * 1915-07-24 1916-02-08 Clarence A Hammond-Knowlton Method of waxing silk thread.
US2113361A (en) * 1933-10-17 1938-04-05 Oca Heriberto Uribe Montes De Treating process for all kinds of fibers
US2150569A (en) * 1936-06-12 1939-03-14 Celanese Corp Textile materials and their preparation
US2310951A (en) * 1941-05-01 1943-02-16 Lloyd C Greene Process and apparatus for forming and treating yarn
US2381020A (en) * 1942-04-23 1945-08-07 Carbide & Carbon Chem Corp Antistatic treatment of vinyl resin textiles
US2393863A (en) * 1942-03-26 1946-01-29 Bakelite Corp Antistatic composition
US2394212A (en) * 1941-08-09 1946-02-05 Celanese Corp Manufacture of artificial products
US2686137A (en) * 1951-11-26 1954-08-10 Monsanto Chemicals Sized yarn and process of sizing
US2742379A (en) * 1954-02-25 1956-04-17 Du Pont Treatment of textile fibers with antistatic agent and product thereof
US2758908A (en) * 1952-06-25 1956-08-14 Du Pont Process of crimping polyethylene terephthalate filaments by heat stretching and heatrelaxing
US2809159A (en) * 1954-11-18 1957-10-08 Dexter Chemical Corp Antistatic and rewetting treatment of textile material
US2865409A (en) * 1955-06-27 1958-12-23 Dietrich V Asten Dryer felt for fine quality paper
US2920980A (en) * 1956-03-28 1960-01-12 Du Pont Finishing fabrics
US2926065A (en) * 1956-04-18 1960-02-23 Fabric Res Lab Inc Method of shrinkproofing oriented, crystallized polyethylene terephthalate yarns at elevated temperatures by heat tensioning and heat relaxing said yarns

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB665914A (en) * 1948-09-01 1952-02-06 Wakefield & Co Ltd C C Improvements in or relating to the anti-static treatment of textile fibres, filaments and yarns
US2702257A (en) * 1950-12-22 1955-02-15 Chicopee Mfg Corp Application of antistatic materials to dielectrics
DE1005235B (en) * 1953-07-11 1957-03-28 Boehme Fettchemie Gmbh Process for the treatment of textile materials
BE542836A (en) * 1953-09-29
US2718478A (en) * 1954-01-27 1955-09-20 American Cyanamid Co Antistatic treatment of fibrous materials

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1171195A (en) * 1915-07-24 1916-02-08 Clarence A Hammond-Knowlton Method of waxing silk thread.
US2113361A (en) * 1933-10-17 1938-04-05 Oca Heriberto Uribe Montes De Treating process for all kinds of fibers
US2150569A (en) * 1936-06-12 1939-03-14 Celanese Corp Textile materials and their preparation
US2310951A (en) * 1941-05-01 1943-02-16 Lloyd C Greene Process and apparatus for forming and treating yarn
US2394212A (en) * 1941-08-09 1946-02-05 Celanese Corp Manufacture of artificial products
US2393863A (en) * 1942-03-26 1946-01-29 Bakelite Corp Antistatic composition
US2381020A (en) * 1942-04-23 1945-08-07 Carbide & Carbon Chem Corp Antistatic treatment of vinyl resin textiles
US2686137A (en) * 1951-11-26 1954-08-10 Monsanto Chemicals Sized yarn and process of sizing
US2758908A (en) * 1952-06-25 1956-08-14 Du Pont Process of crimping polyethylene terephthalate filaments by heat stretching and heatrelaxing
US2742379A (en) * 1954-02-25 1956-04-17 Du Pont Treatment of textile fibers with antistatic agent and product thereof
US2809159A (en) * 1954-11-18 1957-10-08 Dexter Chemical Corp Antistatic and rewetting treatment of textile material
US2865409A (en) * 1955-06-27 1958-12-23 Dietrich V Asten Dryer felt for fine quality paper
US2920980A (en) * 1956-03-28 1960-01-12 Du Pont Finishing fabrics
US2926065A (en) * 1956-04-18 1960-02-23 Fabric Res Lab Inc Method of shrinkproofing oriented, crystallized polyethylene terephthalate yarns at elevated temperatures by heat tensioning and heat relaxing said yarns

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3140957A (en) * 1960-02-23 1964-07-14 Kurashiki Rayon Co Heat treatment of fibers
US3113369A (en) * 1960-05-02 1963-12-10 Monsanto Chemicals Yarn manufacture and products obtained thereby
US4356139A (en) * 1980-12-12 1982-10-26 Southwire Company Method for lubricating cable in a dry curing system

Also Published As

Publication number Publication date
BE559327A (en)
CH377042A (en) 1964-04-30
GB833450A (en) 1960-04-27
DE1105108B (en) 1961-04-20
ES236495A1 (en) 1958-01-16
FR1179107A (en) 1959-05-21

Similar Documents

Publication Publication Date Title
US4497720A (en) Method for treating metallic or ceramic surfaces at high temperatures
US3338830A (en) Textile product
US2990604A (en) Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns
US2976186A (en) Treated textile fiber
US2735790A (en) Ttnitehi
US3756972A (en) Treating agent for thermoplastic synthetic fibers
US2067219A (en) Treatment of filaments, films, and textile fabrics
US4169061A (en) Fiber treating compositions
US3993571A (en) Spin finish for yarn used in food packaging
JPS597828B2 (en) Smoothing agent composition for synthetic fibers with antistatic effect
US2436219A (en) Textile product and process
US4242095A (en) Yarn lubricants
US3563892A (en) Textile-treating composition and process
KR790001757B1 (en) Coning oil
US3505220A (en) Textile-finishing composition and textile treated therewith
US3959534A (en) Process for producing fibers
US2328600A (en) Treatment of textile materials
US2286793A (en) Yarn conditioning process and composition therefor
US2286824A (en) Yarn treating
US2743193A (en) Treated cellulose organic acid ester fibers
KR910009654B1 (en) A lubricant oil composites for manufacturing a synthetic fiber
EP0075261B1 (en) Preparing agent for fibres
US2331664A (en) Yarn conditioning process and composition therefor
US2025435A (en) Treating natural and artificial fibers
KR940000573B1 (en) Composition for thermoplastic synthetic fiber