WO2001014628A1 - Heat stable coning oil - Google Patents
Heat stable coning oil Download PDFInfo
- Publication number
- WO2001014628A1 WO2001014628A1 PCT/EP2000/008209 EP0008209W WO0114628A1 WO 2001014628 A1 WO2001014628 A1 WO 2001014628A1 EP 0008209 W EP0008209 W EP 0008209W WO 0114628 A1 WO0114628 A1 WO 0114628A1
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- WO
- WIPO (PCT)
- Prior art keywords
- fatty acids
- oil according
- winding oil
- winding
- compound
- Prior art date
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Classifications
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
- D06M13/2243—Mono-, di-, or triglycerides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/165—Ethers
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
Definitions
- the present invention relates to winding oil compositions for textile fibers. More particularly, it relates to winding oil compositions for polyester or polyamide fibers.
- compositions used as winding oils must have many properties. In addition to lubricating properties, they must protect metals from corrosion, evacuate electrical charges, and be able to be removed by washing the fiber. In the context of environmental protection, it is also necessary that these compositions do not give pollution by evaporation during the heat treatments carried out on the fibers, and that they have a high biodegradability (in particular with a view to fiber washing operation).
- Document JP-A-55067069 describes a textile oil for polyester fiber comprising at least 50% of esters consisting mainly of fatty acid esters with a trimethylol alkane or pentaerythritol, the other components being monoalcohol esters with fatty acids .
- Textile oil also contains nonionic surfactants, antistatic agents, and anionic surfactants.
- thermal stability is meant the resistance of the composition of winding oils to evaporation during the necessary heat treatments of the fibers.
- the thermal stability is measured objectively by gravimetrically determining the quantity of composition evaporated after heat treatment under standardized conditions; it is expressed in g per kg of textile.
- An object of the invention is to provide winding oil compositions having improved thermal stability.
- Another object of the invention is to provide winding oil compositions which, while retaining good properties, have improved thermal stability.
- Another object of the invention is to provide winding oil compositions for fibers of the polyester or polyamide type, having improved thermal stability.
- compositions of the invention comprise, in addition to the usual additives, essentially a mixture of:
- compositions having a viscosity of less than 70 cSt at 20 ° C.
- the ethoxylated sorbitan triesters preferably comprise from 15 to 25 units of ethylene oxide, the most preferred value being about 20 units of ethylene oxide. They are mainly based on one or more C 18 fatty acids, namely that the C 18 fatty acids represent more than 50 mol% of the fatty acids of the triesters, preferably more than 75%, the most preferred value being at least 90%; among the C18 fatty acids, it is preferable to use mainly oleic acid or isostearic acid, preferably for more than 75 mol% of the C 18 fatty acids.
- the preferred compounds are the sorbitan triesters with the fatty acids d vegetable origin predominantly C 18 (preferably rapeseed or sunflower fatty acids) or mixtures thereof, ethoxylated with approximately 20 units of ethylene oxide; the most preferred compound is the sorbitan trioleate ethoxylated with about 20 units of ethylene oxide.
- the polyethylene glycol diesters preferably comprise from 10 to 20 units of ethylene oxide, the most preferred value being about 15 units of ethylene oxide. They are mainly based on one or more C 18 fatty acids, namely that the C 18 fatty acids represent more than 50 mol% of the fatty acids of the diesters, preferably more than 75%, the most preferred value being at least 90%; among the C18 fatty acids, it is preferred to use mainly oleic acid or isostearic acid, preferably for more than 75 mol% of the fatty acids in Cl 8.
- the preferred diesters are the diesters of PEG 600 (polyethylene glycol of nominal molecular weight equal to 600) with fatty acids of vegetable origin predominantly C18 (preferably rapeseed or sunflower fatty acids), PEG 600 diisostearate, and mixtures thereof.
- the ethoxylated di- and triesters preferably represent from 15 to 25% by weight of the mixture, the most preferred value being approximately 20% by weight.
- the triester of glycerol or of trimethylolpropane is preferably based on fatty acids of vegetable origin predominantly C8 to C12; C8, C10 acids and their mixtures are preferably used, a mixture in equal parts in moles being particularly preferred.
- the usual additives and the concentrations to be used are well known to those skilled in the art.
- These usual additives essentially comprise at least one antistatic agent (to improve the antistatic power), generally present at a rate of 1 to 3% by weight of the composition, as well as at least one antioxidant agent (to prevent oxidation of the components during heat treatment operations) and at least one wetting agent (to promote spreading of the size on the fibers), generally present in an amount of less than 1% by weight of the composition.
- the ingredients are chosen so that the viscosity of the compositions of the invention is preferably between 30 and 60 cSt at 20 ° C, the most preferred value being between 40 and 55 cSt at 20 ° C.
- compositions are used as winding oil for fibers of the polyester or polyamide type; they are particularly suitable for polyester type fibers.
- the invention also relates to a process for winding polyester or polyamide type fibers in which a composition as described is used as winding oil.
- thermal stability is the difference between the weight after 15 min at 50 ° C and the weight after 15 min at 180 ° C, expressed in% of 1 g.
- the sample is placed in the material holder of an ILMA washing device, the cup of which contains 200 ml of washing bath; • washing for 20 min at 20 ° C, in a neutral aqueous medium, without detergent, at the rate of 10 cycles / min of vertical movement of the sample in the cup;
- the polyester fiber is unwound through the calender, first passes over a lick roller system which applies the size, then through the two drying zones before being rewound.
- the operating conditions are as follows:
- the emission factor expressed in g / g of textile, is calculated by making the ratio of the flow rate of the winding oil emitted (in g / h; concentration in air x air flow rate) over the flow rate of winding oil captured by the fiber (in kg / h).
- composition comprising:
- additives comprising an antistatic additive, an antioxidant additive and a wetting agent.
- the composition had a viscosity of 50 cSt at 20 ° C. Its properties have been measured as winding oil; the values are given in table 1.
- Table 1 shows that the composition of Example 1 has better thermal stability and a better coefficient of friction than that of Comparative Example A, the antistatic and washing properties being able to be considered as equivalent.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Lubricants (AREA)
- Pistons, Piston Rings, And Cylinders (AREA)
- Organic Insulating Materials (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
HUILE DE BOBINAGE THERMOSTABLE THERMOSTABLE WINDING OIL
La présente invention concerne des compositions d'huiles de bobinage pour fibres textiles. Plus particulièrement, elle concerne des compositions d'huiles de bobinage pour fibres polyester ou polyamide.The present invention relates to winding oil compositions for textile fibers. More particularly, it relates to winding oil compositions for polyester or polyamide fibers.
Les compositions utilisées comme huiles de bobinage doivent posséder de nombreuses propriétés. En plus de propriétés lubrifiantes, elles doivent protéger les métaux de la corrosion, évacuer les charges électriques, et pouvoir être enlevées par lavage de la fibre. Dans le cadre de la protection de l'environnement, il convient en plus que ces compositions ne donnent pas de pollution par évaporation lors des traitements thermiques effectués sur les fibres, et qu'elles aient une biodégradabilité élevée (en particulier en vue de l'opération de lavage des fibres).The compositions used as winding oils must have many properties. In addition to lubricating properties, they must protect metals from corrosion, evacuate electrical charges, and be able to be removed by washing the fiber. In the context of environmental protection, it is also necessary that these compositions do not give pollution by evaporation during the heat treatments carried out on the fibers, and that they have a high biodegradability (in particular with a view to fiber washing operation).
Le document US-A-3834870 décrit l'utilisation d'esters d'acides gras en C8-C20 avec des alcools de formule R(OH)x (dans laquelle R est un radical al yle en C5-C20 et x=l-5) comme huile de bobinage ("coning oil") pour fibres de polypropylène.Document US-A-3834870 describes the use of C8-C20 fatty acid esters with alcohols of formula R (OH) x (in which R is an al yl radical in C5-C20 and x = l- 5) as "coning oil" for polypropylene fibers.
Le document EP-A-54953 décrit une huile de finition ("spin finish") pour fibres synthétiques comprenant (a) 50-90% d'un lubrifiant thermiquement stable et (b) 10-50% d'un composé de formule R-O-(Aa-Bb)H dans lequel R est un radical alkyle C6-C14, A est oxypropylène, B est oxyethylène, a = 4- 15 et b = 5-10.Document EP-A-54953 describes a spin finish for synthetic fibers comprising (a) 50-90% of a thermally stable lubricant and (b) 10-50% of a compound of formula RO - (Aa-Bb) H in which R is a C6-C14 alkyl radical, A is oxypropylene, B is oxyethylene, a = 4- 15 and b = 5-10.
Le document JP-A-55067069 décrit une huile textile pour fibre polyester comprenant au moins 50 % d'esters consistant principalement en esters d'acides gras avec un triméthylol alkane ou le pentaérythritol, les autres composants étant des esters de monoalcools avec des acides gras. L'huile textile contient également des surfactants non-ioniques, des agents antistatiques, et des surfactants anioniques.Document JP-A-55067069 describes a textile oil for polyester fiber comprising at least 50% of esters consisting mainly of fatty acid esters with a trimethylol alkane or pentaerythritol, the other components being monoalcohol esters with fatty acids . Textile oil also contains nonionic surfactants, antistatic agents, and anionic surfactants.
Le document EP-A-288620 décrit un procédé de traitement de fibres synthétiques destinées à subir un traitement thermique sévère par (a) l'ester d'un acide polycarboxylique et d'un alcool de formule R1R2CH- CH2-O-(AO)nH (avec RI et R2 = alkyle C4-C18, AO= oxyde d'alkylene en C2-C4 et n=0-30) ou (b) l'ester d'un alcool polyhydrique et d'un acide de formule R3R4CH-COOH (avec R3 et R4 = alkyle C4-C18).Document EP-A-288620 describes a process for treating synthetic fibers intended to undergo a severe heat treatment with (a) the ester of a polycarboxylic acid and an alcohol of formula R1R2CH- CH2-O- (AO) nH (with RI and R2 = C4-C18 alkyl, AO = alkylene oxide in C2-C4 and n = 0-30) or (b) the ester of a polyhydric alcohol and of an acid of formula R3R4CH-COOH (with R3 and R4 = C4-C18 alkyl).
Plusieurs articles de W. Dόhrn et al. décrivent un produit commercial présentant notamment des propriétés de résistance à l'évaporation ("low- emission"):Several articles by W. Dόhrn et al. describe a commercial product exhibiting in particular resistance to evaporation ("low-emission"):
- Melliand Int. (1998), (1), 8, 10;- Melliand Int. (1998), (1), 8, 10;
- Melliand Textilber., (1998), 79(3), 130-1, E28-9;- Melliand Textilber., (1998), 79 (3), 130-1, E28-9;
- Melliand Int. (1996), (4), 180-4;- Melliand Int. (1996), (4), 180-4;
- Melliand Textilber., (1996), 77(11), 770-4, E171- 1.- Melliand Textilber., (1996), 77 (11), 770-4, E171-1.
Il existe des ensimages composés d'émulsions ou de solutions aqueuses, mais l'utilisation industrielle de ces ensimages n'est pas fiable du fait de l'évaporation de l'eau qui fait augmenter la concentration et donc la viscosité du produit; il en résulte des variations importantes et difficilement contrôlables de la quantité d'ensimage prélevée par les fils, en particulier en cas d'application de l'ensimage par un système de rouleau lècheur.There are sizes composed of emulsions or aqueous solutions, but the industrial use of these sizes is not reliable due to the evaporation of water which increases the concentration and therefore the viscosity of the product; this results in large and difficult to control variations in the amount of size taken up by the wires, in particular in the case of application of the size by a lick roller system.
Toutefois, les compositions connues d'huiles de bobinage anhydres ne présentent pas une stabilité thermique suffisante. On entend par stabilité thermique la résistance de la composition d'huiles de bobinage à l'évaporation lors des traitements thermiques nécessaires des fibres. La stabilité thermique est mesurée objectivement en déterminant gravimétriquement la quantité de composition évaporée après traitement thermique dans des conditions standardisées; elle est exprimée en g par kg de textile.However, the known compositions of anhydrous winding oils do not have sufficient thermal stability. By thermal stability is meant the resistance of the composition of winding oils to evaporation during the necessary heat treatments of the fibers. The thermal stability is measured objectively by gravimetrically determining the quantity of composition evaporated after heat treatment under standardized conditions; it is expressed in g per kg of textile.
Il existe donc un besoin pour des compositions d'huiles de bobinage ayant une stabilité thermique améliorée.There is therefore a need for winding oil compositions having improved thermal stability.
Un objet de l'invention est de fournir des compositions d'huiles de bobinage ayant une stabilité thermique améliorée.An object of the invention is to provide winding oil compositions having improved thermal stability.
Un autre objet de l'invention est de fournir des compositions d'huiles de bobinage qui, tout en conservant de bonnes propriétés, ont une stabilité thermique améliorée. L'invention a encore pour objet de fournir des compositions d'huiles de bobinage pour fibres de type polyester ou polyamide, ayant une stabilité thermique améliorée.Another object of the invention is to provide winding oil compositions which, while retaining good properties, have improved thermal stability. Another object of the invention is to provide winding oil compositions for fibers of the polyester or polyamide type, having improved thermal stability.
Les compositions de l'invention comprennent, en plus des additifs usuels, essentiellement un mélange de:The compositions of the invention comprise, in addition to the usual additives, essentially a mixture of:
- 10 à 30 % en poids d'un composé choisi dans le groupe comprenant les triesters de sorbitan éthoxylé, les diesters de polyethylene glycol et leurs mélanges, comprenant de 10 à 30 unités d'oxyde d'éthylène, et dans lequel l'ester est majoritairement à base d'un ou plusieurs acides gras en C 18;- 10 to 30% by weight of a compound chosen from the group comprising ethoxylated sorbitan triesters, polyethylene glycol diesters and mixtures thereof, comprising from 10 to 30 units of ethylene oxide, and in which the ester is mainly based on one or more C 18 fatty acids;
- 90 à 70 % en poids d'un triester de glycerol ou de trimethylolpropane avec des acides gras choisis dans le groupe comprenant les acides en C8, C9, C 10, C i l , C 12 et leurs mélanges; les compositions ayant une viscosité inférieure à 70 cSt à 20°C.- 90 to 70% by weight of a triester of glycerol or trimethylolpropane with fatty acids chosen from the group comprising C8, C9, C 10, C i l, C 12 acids and their mixtures; compositions having a viscosity of less than 70 cSt at 20 ° C.
Les triesters de sorbitan éthoxylé comprennent de préférence de 15 à 25 unités d'oxyde d'éthylène, la valeur la plus préférée étant environ 20 unités d'oxyde d'éthylène. Ils sont majoritairement à base d'un ou plusieurs acides gras en C 18, à savoir que les acides gras en C18 représentent plus de 50 % en moles des acides gras des triesters, de préférence plus de 75 %, la valeur la plus préférée étant d'au moins 90%; parmi les acides gras en C18, on préfère utiliser majoritairement l'acide oléique ou l'acide isostéarique, de préférence pour plus de 75 % en moles des acides gras en C 18. Les composés préférés sont les triesters de sorbitan avec les acides gras d'origine végétale majoritairement en C 18 (de préférence les acides gras de colza ou de tournesol) ou leurs mélanges, éthoxylés avec environ 20 unités d'oxyde d'éthylène; le composé le plus préféré est le trioléate de sorbitan éthoxylé avec environ 20 unités d'oxyde d'éthylène.The ethoxylated sorbitan triesters preferably comprise from 15 to 25 units of ethylene oxide, the most preferred value being about 20 units of ethylene oxide. They are mainly based on one or more C 18 fatty acids, namely that the C 18 fatty acids represent more than 50 mol% of the fatty acids of the triesters, preferably more than 75%, the most preferred value being at least 90%; among the C18 fatty acids, it is preferable to use mainly oleic acid or isostearic acid, preferably for more than 75 mol% of the C 18 fatty acids. The preferred compounds are the sorbitan triesters with the fatty acids d vegetable origin predominantly C 18 (preferably rapeseed or sunflower fatty acids) or mixtures thereof, ethoxylated with approximately 20 units of ethylene oxide; the most preferred compound is the sorbitan trioleate ethoxylated with about 20 units of ethylene oxide.
Les diesters de polyethylene glycol comprennent de préférence de 10 à 20 unités d'oxyde d'éthylène, la valeur la plus préférée étant environ 15 unités d'oxyde d'éthylène. Ils sont majoritairement à base d'un ou plusieurs acides gras en C 18, à savoir que les acides gras en C18 représentent plus de 50 % en moles des acides gras des diesters, de préférence plus de 75 %, la valeur la plus préférée étant d'au moins 90%; parmi les acides gras en C18, on préfère utiliser majoritairement l'acide oléique ou l'acide isostéarique, de préférence pour plus de 75 % en moles des acides gras en Cl 8. Les diesters préférés sont les diesters de PEG 600 (polyethylene glycol de poids moléculaire nominal égal à 600) avec les acides gras d'origine végétale majoritairement en C18 (de préférence les acides gras de colza ou de tournesol), le diisostéarate de PEG 600, et leurs mélanges.The polyethylene glycol diesters preferably comprise from 10 to 20 units of ethylene oxide, the most preferred value being about 15 units of ethylene oxide. They are mainly based on one or more C 18 fatty acids, namely that the C 18 fatty acids represent more than 50 mol% of the fatty acids of the diesters, preferably more than 75%, the most preferred value being at least 90%; among the C18 fatty acids, it is preferred to use mainly oleic acid or isostearic acid, preferably for more than 75 mol% of the fatty acids in Cl 8. The preferred diesters are the diesters of PEG 600 (polyethylene glycol of nominal molecular weight equal to 600) with fatty acids of vegetable origin predominantly C18 (preferably rapeseed or sunflower fatty acids), PEG 600 diisostearate, and mixtures thereof.
Les di- et triesters éthoxylés représentent de préférence de 15 à 25 % en poids du mélange, la valeur la plus préférée étant d'environ 20 % en poids.The ethoxylated di- and triesters preferably represent from 15 to 25% by weight of the mixture, the most preferred value being approximately 20% by weight.
Le triester de glycerol ou de trimethylolpropane est de préférence à base d'acides gras d'origine végétale majoritairement en C8 à C 12; on utilise de préférence les acides en C8, C10 et leurs mélanges, un mélange à parts égales en môles étant particulièrement préféré.The triester of glycerol or of trimethylolpropane is preferably based on fatty acids of vegetable origin predominantly C8 to C12; C8, C10 acids and their mixtures are preferably used, a mixture in equal parts in moles being particularly preferred.
Les additifs usuels et les concentrations à mettre en oeuvre sont bien connus de l'homme de métier. Ces additifs usuels comprennent essentiellement au moins un agent antistatique (pour améliorer le pouvoir antistatique), généralement présent à raison de 1 à 3 % en poids de la composition, ainsi qu'au moins un un agent antioxydant (pour éviter l'oxydation des composants lors des opérations de traitement thermique) et au moins un agent mouillant (pour favoriser l'étalement de l'ensimage sur les fibres), généralement présents à raison de moins de 1 % en poids de la composition.The usual additives and the concentrations to be used are well known to those skilled in the art. These usual additives essentially comprise at least one antistatic agent (to improve the antistatic power), generally present at a rate of 1 to 3% by weight of the composition, as well as at least one antioxidant agent (to prevent oxidation of the components during heat treatment operations) and at least one wetting agent (to promote spreading of the size on the fibers), generally present in an amount of less than 1% by weight of the composition.
Les ingrédients sont choisis de manière à ce que la viscosité des compositions de l'invention soit de préférence comprise entre 30 et 60 cSt à 20°C, la valeur la plus préférée étant entre 40 et 55 cSt à 20°C.The ingredients are chosen so that the viscosity of the compositions of the invention is preferably between 30 and 60 cSt at 20 ° C, the most preferred value being between 40 and 55 cSt at 20 ° C.
Ces compositions sont utilisées comme huile de bobinage pour fibres de type polyester ou polyamide; elles conviennent tout particulièrement aux fibres de types polyester.These compositions are used as winding oil for fibers of the polyester or polyamide type; they are particularly suitable for polyester type fibers.
L'invention concerne également un procédé de bobinage de fibres de type polyester ou polyamide dans lequel on utilise comme huile de bobinage une composition telle que décrite. EXEMPLESThe invention also relates to a process for winding polyester or polyamide type fibers in which a composition as described is used as winding oil. EXAMPLES
Dans les exemples, on a mesuré les différentes propriétés comme suit :In the examples, the various properties were measured as follows:
Stabilité thermique en couche minceThin layer thermal stability
• on dépose 1 g du produit à tester sur un disque de fibre de verre de 90 mm de diamètre placé dans un appareil de thermogravimétric;• 1 g of the product to be tested is placed on a 90 mm diameter glass fiber disc placed in a thermogravimetric device;
• on porte la température d'abord à 50°C pendant 15 min, puis à 180°C pendant 15 min;• the temperature is brought first to 50 ° C for 15 min, then to 180 ° C for 15 min;
• la stabilité thermique est la différence entre le poids après 15 min à 50°C et le poids après 15 min à 180°C, exprimée en % de 1 g.• thermal stability is the difference between the weight after 15 min at 50 ° C and the weight after 15 min at 180 ° C, expressed in% of 1 g.
Coefficient de frottementCoefficient of friction
• on fait passer à 20°C et 65% d'humidité relative, un fil de polyester 167/48 FTF sur le frotteur en acier poli d'un appareil F-meter de ROTHSCHILD;• 167/48 FTF polyester wire is passed at 20 ° C and 65% relative humidity on the polished steel wiper of an ROTHSCHILD F-meter device;
• on mesure la tension d'entrée et la tension de sortie du fil à l'aide de tensiomètres électroniques, et on en déduit le coefficient de frottement par la formule de frottement de corde dΕytelwein.• one measures the tension of entry and the tension of exit of the wire using electronic tensiometers, and one deduces from it the coefficient of friction by the formula of friction of cord dΕytelwein.
Pouvoir antistatiqueAntistatic power
• on mesure à l'aide d'un voltmètre statique R-4021 de ROTHSCHILD le temps mis par une borne de mesure, portée à 150 V, pour se décharger de moitié à travers 10 fils de 10 cm et une borne reliée à la terre, le tout à 20°C et 65% d'humidité relative.• using a ROTHSCHILD static voltmeter R-4021, measure the time taken by a measurement terminal, brought to 150 V, to discharge half through 10 x 10 cm wires and a terminal connected to earth , all at 20 ° C and 65% relative humidity.
Test de lavage (pesées et séchage à 20°C et 65% d'humidité relative)Washing test (weighing and drying at 20 ° C and 65% relative humidity)
• on pèse exactement un échantillon d'environ 10 g de textile polyester• a sample of approximately 10 g of polyester textile is weighed exactly
(a) ;(at) ;
• on dépose environ 0,5 g d'ensimage au milieu de l'échantillon de textile;• approximately 0.5 g of size is deposited in the middle of the textile sample;
• on laisse reposer 24 h puis on pèse à nouveau le textile (b) ;• leave to stand for 24 hours and then weigh the textile again (b);
• on place l'échantillon dans la porte -matière d'un appareil de lavage ILMA dont le godet contient 200 ml de bain de lavage; • on lave pendant 20 min à 20°C, en milieu aqueux neutre, sans détergent, à raison de 10 cycles/ min de déplacement vertical de l'échantillon dans le godet;• the sample is placed in the material holder of an ILMA washing device, the cup of which contains 200 ml of washing bath; • washing for 20 min at 20 ° C, in a neutral aqueous medium, without detergent, at the rate of 10 cycles / min of vertical movement of the sample in the cup;
• après essorage pendant 3 min, on laisse sécher pendant 24 h avant de peser l'échantillon (c);• after spinning for 3 min, it is left to dry for 24 h before weighing the sample (c);
• on exprime en % la quantité d'ensimage éliminée par lavage à l'aide de la formule• the quantity of size removed by washing is expressed in% using the formula
100 [(b-a)/b-(c-a)/c]/ [(b-a)/b]100 [(b-a) / b- (c-a) / c] / [(b-a) / b]
Biodé radabilitéBiodegradability
• la méthode utilisée porte la référence C.E.C. L33 T82• the method used bears the reference C.E.C. L33 T82
Stabilité thermique sur fibres.Thermal stability on fibers.
On a utilisé un appareil de bobinage de taille laboratoire ayant les caractéristiques suivantes :A laboratory-sized winding apparatus having the following characteristics was used:
- fabricant : Werner Mathis, Zurich (1973)- manufacturer: Werner Mathis, Zurich (1973)
- modèle : T II- model: T II
- zones de séchage : deux (1,3 m chacune)- drying zones: two (1.3 m each)
- ventilateur de sortie : Werner Mathis VZA 1 1993 (0,4 kW)- outlet fan: Werner Mathis VZA 1 1993 (0.4 kW)
- calandre : Werner Mathis VF 4073 (0,58 kW, 0,4- 15 m/min, 0, 1 bar)- grille: Werner Mathis VF 4073 (0.58 kW, 0.4- 15 m / min, 0.1 bar)
La fibre polyester est déroulée par la calandre, passe d'abord sur un système de rouleau lècheur qui applique l'ensimage puis dans les deux zones de séchage avant d'être rebobinée. Les conditions opératoires sont les suivantes :The polyester fiber is unwound through the calender, first passes over a lick roller system which applies the size, then through the two drying zones before being rewound. The operating conditions are as follows:
- température dans les zones de séchage : 190°C- temperature in the drying zones: 190 ° C
- temps de séchage : 1 ,5 minutes prise d'ensimage : 1% du poids de fibre- drying time: 1.5 minutes size setting: 1% of the weight of fiber
On calcule le facteur d'émission, exprimé en g/ g de textile, en faisant le rapport du débit d'huile de bobinage émise (en g/ h ; concentration dans l'air x débit d'air) sur le débit d'huile de bobinage saisie par la fibre (en kg/h). EXEMPLE 1The emission factor, expressed in g / g of textile, is calculated by making the ratio of the flow rate of the winding oil emitted (in g / h; concentration in air x air flow rate) over the flow rate of winding oil captured by the fiber (in kg / h). EXAMPLE 1
On a préparé une composition comprenant:A composition was prepared comprising:
- 80 parties en poids de triester de glycerol avec un mélange d'acides gras en C8 et CIO, d'une viscosité de 16 mm2/s à 40°C;- 80 parts by weight of glycerol triester with a mixture of C8 and CIO fatty acids, with a viscosity of 16 mm2 / s at 40 ° C;
- 18 parties en poids de trioléate de sorbitan éthoxylé (20 unités d'oxyde d'éthylène), d'une viscosité de 110 mm2/s à 40°C;- 18 parts by weight of ethoxylated sorbitan trioleate (20 units of ethylene oxide), with a viscosity of 110 mm2 / s at 40 ° C;
- 2 parties en poids d'additifs (comprenant un additif antistatique, un additif antioxydant et un agent mouillant).- 2 parts by weight of additives (comprising an antistatic additive, an antioxidant additive and a wetting agent).
La composition avait une viscosité de 50 cSt à 20°C. On a mesuré ses propriétés en tant qu'huile de bobinage; les valeurs sont reprises dans le tableau 1.The composition had a viscosity of 50 cSt at 20 ° C. Its properties have been measured as winding oil; the values are given in table 1.
EXEMPLE COMPARATIF ACOMPARATIVE EXAMPLE A
On a mesuré les propriétés de l'huile de bobinage vendue sous la dénomination Tallopol 7496 (Tallopol est une marque de la société Stockhausen, décrite dans les publications de W. Dohrn et al. citées plus haut). Les valeurs sont reprises dans le tableau 1.The properties of the winding oil sold under the name Tallopol 7496 were measured (Tallopol is a trademark of the company Stockhausen, described in the publications by W. Dohrn et al. Cited above). The values are given in table 1.
TABLEAU 1TABLE 1
Propriété Ex. 1 Ex. comp. A Fil non ensiméProperty Ex. 1 Comp. Ex. A Non-sized wire
stabilité thermique 2, 1 % 2,9 % (non applicable)thermal stability 2.1% 2.9% (not applicable)
(couche mince) coefficient de frottement 0,38 0,47 0,48 pouvoir antistatique 4 s 3 s 34 s test de lavage 86 % 92 % (non applicable) biodégradabilité 90 % (non mesurée) (non applicable) stabilité thermique 0.8 g/kg (non mesurée) (non pplicable)(thin layer) coefficient of friction 0.38 0.47 0.48 antistatic power 4 s 3 s 34 s washing test 86% 92% (not applicable) biodegradability 90% (not measured) (not applicable) thermal stability 0.8 g / kg (not measured) (not applicable)
(sur fibres) Le tableau 1 montre que la composition de l'exemple 1 a une meilleure stabilité thermique et un meilleur coefficient de frottement que celle de l'exemple comparatif A, les propriétés antistatique et de lavage pouvant être considérées comme équivalentes. (on fibers) Table 1 shows that the composition of Example 1 has better thermal stability and a better coefficient of friction than that of Comparative Example A, the antistatic and washing properties being able to be considered as equivalent.
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU69987/00A AU6998700A (en) | 1999-08-13 | 2000-08-21 | Heat stable coning oil |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99402055A EP1077280B1 (en) | 1999-08-13 | 1999-08-13 | Thermostable coning oil |
| EP99402055.0 | 1999-08-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2001014628A1 true WO2001014628A1 (en) | 2001-03-01 |
Family
ID=8242084
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2000/008209 Ceased WO2001014628A1 (en) | 1999-08-13 | 2000-08-21 | Heat stable coning oil |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1077280B1 (en) |
| AT (1) | ATE328148T1 (en) |
| AU (1) | AU6998700A (en) |
| DE (1) | DE69931628T2 (en) |
| WO (1) | WO2001014628A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3327180A1 (en) * | 2016-11-25 | 2018-05-30 | Dako Ag | Use of a preparation liquid with low viscosity and a low water content for treating threads |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU45258A1 (en) * | 1963-01-23 | 1964-03-20 | ||
| FR2197076A1 (en) * | 1972-08-25 | 1974-03-22 | Ici America Inc | |
| FR2317411A1 (en) * | 1975-06-27 | 1977-02-04 | Hoechst Ag | BITTING AGENTS FOR TEXTURING POLYESTER FIBERS |
| EP0288620A1 (en) * | 1987-04-27 | 1988-11-02 | Kao Corporation | Fiber treating process and composition used therefor |
| US4946375A (en) * | 1987-07-15 | 1990-08-07 | E. I. Du Pont De Nemours And Company | Low temperature finish |
| US5358648A (en) * | 1993-11-10 | 1994-10-25 | Bridgestone/Firestone, Inc. | Spin finish composition and method of using a spin finish composition |
-
1999
- 1999-08-13 EP EP99402055A patent/EP1077280B1/en not_active Expired - Lifetime
- 1999-08-13 AT AT99402055T patent/ATE328148T1/en not_active IP Right Cessation
- 1999-08-13 DE DE69931628T patent/DE69931628T2/en not_active Expired - Lifetime
-
2000
- 2000-08-21 AU AU69987/00A patent/AU6998700A/en not_active Abandoned
- 2000-08-21 WO PCT/EP2000/008209 patent/WO2001014628A1/en not_active Ceased
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU45258A1 (en) * | 1963-01-23 | 1964-03-20 | ||
| FR2197076A1 (en) * | 1972-08-25 | 1974-03-22 | Ici America Inc | |
| FR2317411A1 (en) * | 1975-06-27 | 1977-02-04 | Hoechst Ag | BITTING AGENTS FOR TEXTURING POLYESTER FIBERS |
| EP0288620A1 (en) * | 1987-04-27 | 1988-11-02 | Kao Corporation | Fiber treating process and composition used therefor |
| US4946375A (en) * | 1987-07-15 | 1990-08-07 | E. I. Du Pont De Nemours And Company | Low temperature finish |
| US5358648A (en) * | 1993-11-10 | 1994-10-25 | Bridgestone/Firestone, Inc. | Spin finish composition and method of using a spin finish composition |
Also Published As
| Publication number | Publication date |
|---|---|
| AU6998700A (en) | 2001-03-19 |
| EP1077280B1 (en) | 2006-05-31 |
| DE69931628T2 (en) | 2007-04-26 |
| ATE328148T1 (en) | 2006-06-15 |
| EP1077280A1 (en) | 2001-02-21 |
| DE69931628D1 (en) | 2006-07-06 |
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