EP1530657B1 - Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac - Google Patents

Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac Download PDF

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Publication number
EP1530657B1
EP1530657B1 EP03732455A EP03732455A EP1530657B1 EP 1530657 B1 EP1530657 B1 EP 1530657B1 EP 03732455 A EP03732455 A EP 03732455A EP 03732455 A EP03732455 A EP 03732455A EP 1530657 B1 EP1530657 B1 EP 1530657B1
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EP
European Patent Office
Prior art keywords
sorbitan
formulation
weight
ethylene oxide
oxide units
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EP03732455A
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German (de)
English (en)
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EP1530657A1 (fr
Inventor
Hubert Dobbelstein
Shefqet Emini
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EMINI, SHEFQET
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Shefqet Emini
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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
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • D06M13/2243Mono-, di-, or triglycerides
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24DCIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
    • A24D3/00Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
    • A24D3/06Use of materials for tobacco smoke filters
    • A24D3/08Use of materials for tobacco smoke filters of organic materials as carrier or major constituent
    • A24D3/10Use of materials for tobacco smoke filters of organic materials as carrier or major constituent of cellulose or cellulose derivatives
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24DCIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
    • A24D3/00Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
    • A24D3/06Use of materials for tobacco smoke filters
    • A24D3/14Use of materials for tobacco smoke filters of organic materials as additive
    • 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
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/02Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
    • 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
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • 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
    • 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
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
    • D06M2101/08Esters or ethers of cellulose
    • 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 present invention relates to a formulation for use as a lubricant in the manufacture of filaments.
  • the threads are first prepared by a spinning process, which is preferably the solvent spinning process, and then further processed by applying the formulation of the invention on the surface of the threads as a lubricant.
  • the threads produced are preferably cellulose acetate threads and these threads are used to make filters for tobacco products, especially cigarette filters.
  • the patent GB 896,599 describes tobacco filters that can be used in cigarettes, pipes, cigarette holders or cigar tips.
  • the filter elements described consist of bundles of continuous synthetic filaments, wherein water-insoluble calcium or magnesium salts are finely distributed on the surface of the filaments. These finely divided particles are fixed by oils on the fibers. In addition to mineral oils, these oils may also be high-boiling liquid esters of natural origin, liquid esters of natural fats or liquid high molecular weight fatty alcohols.
  • the patent GB 765,962 describes a tobacco filter element consisting of cellulose acetate fibers.
  • the cellulose acetate filter material is subjected to various processing steps, such as stretching and crimping of the fibers.
  • electrostatic charging of the fibers must be prevented, and on the other hand, the surface of the fiber must be provided with a lubricant so that the fiber can be subjected to these processing steps.
  • This lubricant contains a mineral oil with a purity that would make it suitable for the manufacture of pharmaceutical products.
  • a rigid tobacco smoke filter consisting of a bundle of optionally crimped continuous filaments and a paper wrapper is described.
  • the filaments consist of a mixture of a polyalphaolefin and a plasticizer-soluble polymer of an organic plasticizer.
  • Liquid organic plasticizers which can be used in addition to light, medium and heavy mineral oils, liquid high-boiling organic esters or water-insoluble propylene glycols or polybutylene glycols.
  • a cleaning composition containing white mineral oil is described.
  • the emulsion is used for the treatment and cleaning of metal surfaces.
  • the emulsion of the invention contains 20-50 wt.% Of a mineral oil having a viscosity of 50-380 Saybolt seconds, measured at 100 ° F and 0.5 to 10 wt.% Of an emulsifier.
  • nonionic emulsifiers has been found to be advantageous.
  • sorbitan esters and polyglycerides of fatty acids are also mentioned.
  • emulsifier should be present in the emulsion as is just necessary to form a stable emulsion. In this case, 0.5 to 10% by weight of the emulsifier are present in the emulsion, with 1 to 5% by weight of emulsifier being preferred. If more emulsifier is present in the emulsion, milky stains or streaks may remain on the cleaned surface after cleaning.
  • a thread which normally contains cellulose acetate
  • a spinning process which is preferably the solvent spinning process.
  • an acetone solution of cellulose acetate and matting agent TiO 2 is pressed through shower-like nozzles (spinnerets).
  • the holes usually have cross sections in the form of an equilateral triangle.
  • a heated spin shaft Below the spinnerets is a heated spin shaft. The air sucked through the spinning shaft heats up and absorbs the solvent which diffuses out of the formed filament, acetone, which almost is completely recovered.
  • the solution solidifies under considerable volume shrinkage to a filament.
  • the filaments When using triangular holes, the filaments have a Y-section.
  • the filaments in the thread When a thread composed of several filaments leaves the spinning shaft, the filaments in the thread are densely packed without, however, sticking to each other.
  • the thread At the exit of the spinning shaft, the thread typically contains a residual fraction of about 1 to 6% by weight of acetone.
  • the thread is provided with a preparation (avivage), which serves mainly as a lubricant for the subsequent processing steps. This preparation is carried out by an oiler or by means of an applicator roll.
  • the content of acetone in the threads is first further reduced, a plurality of threads are combined to form the so-called rope and the rope is subjected to a crimping process by means of a crimping machine, which preferably works according to the stuffer box principle.
  • this rope is passed through a conical machine part and thus compressed to its final thickness, ie the thickness of the filter to be produced.
  • a glycerol triacetate-containing composition is applied to the filter tow. This further preparation, after leaving the compression part by curing, fixes the filter in the desired shape and thickness.
  • the formulation applied after the threads have dried acts as a lubricant. It ensures, inter alia, that the friction which occurs during the subsequent processing steps does not exceed a value which leads to the breakage or undesired heating of the threads or the rope. Both would cause unwanted rejects.
  • the lubricant enables higher machine speeds. The formulation must withstand the high shear forces associated with this process without loss of effect.
  • This lubricant usually consists of an emulsion which is prepared from a mixture of low-viscosity mineral oil and emulsifier. Other components may be included in the emulsion.
  • the mineral oils remain on the threads after the manufacture of the filters and the corresponding tobacco products containing these filters. For example, when smoking a cigarette containing such a filter, some of the mineral oil that is on the filter may be absorbed by the smoker.
  • MK Baldwin et al. MK Baldwin et al .; "Feeding studies in council with mineral hydrocarbon grade grade white mineral oils", Toxicol. Pathol. 20, 426 (1992 )
  • Smith et al. JH Smith et al .; "Ninety-day feeding study in Fischer's 344-rats highly refined petroleum-derived food-grade white oils and waxes", Toxicol. Pathol.
  • the object of the present invention is to provide a stable and storable emulsion containing high viscosity mineral oils having a viscosity of at least 8.5 mm 2 / s at 100 ° C. For this it is necessary to find emulsifiers for the preparation of a processible formulation. The formulation is then used in exchange for the formulations containing low viscosity mineral oils.
  • the object of the present invention is achieved by a formulation for use as a preparation in the production of threads containing a) 30-80 wt .-% of a mineral oil having a viscosity of at least 8.5 mm 2 / s at 100 ° C and b) 11 60% by weight of an emulsifier selected from sorbitan monoesters, derivatives of sorbitan monoesters, sorbitan diesters, derivatives of sorbitan diesters, sorbitan triesters, derivatives of sorbitan triesters, polyglycerol esters, derivatives of polyglycerol esters, polyricinoleate, derivatives of polyricinoleate and mixtures thereof, the formulation comprising a water in oil or an oil-in-water emulsion.
  • an emulsifier selected from sorbitan monoesters, derivatives of sorbitan monoesters, sorbitan diesters, derivatives of sorbitan diesters, sorbitan
  • the stability of a formulation which may be in the form of an emulsion can be determined by the turbidity of the formulation. It basically applies that a higher turbidity indicates a lower stability.
  • the processing stability of the formulation can be checked by checking the turbidity of the formulation during processing. No or little increase in turbidity is particularly advantageous, while a greater increase in turbidity indicates inadequate formulation stability.
  • the storage stability of a formulation can be checked by checking the turbidity after, for example, five days storage at 23 ° C.
  • the viscosity at 100 ° C. is at least 8.5 mm 2 / s.
  • the mineral oil used preferably has a viscosity of from 8.5 to 1000, particularly preferably from 8.5 to 20 and very particularly preferably from 8.5 to 11 mm 2 / s.
  • the proportion of hydrocarbons in the high-viscosity mineral oil having less than 25 carbon atoms is not more than 5% by weight.
  • the average molecular weight of the high-viscosity mineral oil should not be less than 480 g / mol.
  • the emulsifiers used according to the invention are selected from sorbitan monoesters, derivatives of sorbitan monoesters, sorbitan diesters, derivatives of sorbitan diesters, sorbitan triesters, derivatives of sorbitan triesters, polyglycerol esters, derivatives of polyglycerol esters and mixtures thereof.
  • the esters may preferably be esters with fatty acids.
  • the fatty acid all fatty acids can be used, such as e.g. Stearic acid, oleic acid, lauric acid and ricinoleic acid ([R (Z)] - 12-hydroxy-9-octadecenoic acid).
  • the fatty acids used may alternatively be derived from corn, cottonseed oil, palm oil, peanut oil, sesame oil, soybean oil, safflower oil, castor oil or other oils of native origin.
  • the fatty acids can be hydrogenated or non-hydrogenated, and condensed or non-condensed.
  • the sorbitan triester be selected from the group consisting of sorbitan triesters with fatty acids containing 10-25 carbon atoms, ethoxylated sorbitan triesters with fatty acids containing 10-25 carbons and containing 5-30 moles of ethylene oxide units per mole of sorbitan triester, and mixtures thereof.
  • the sorbitan triester may be selected from the group consisting of sorbitan tristearate, ethoxylated sorbitan tristearate with 5-30 moles of ethylene oxide units per mole of sorbitan tristearate, sorbitan trioleate, ethoxylated sorbitan trioleate with 5-30 mole ethylene oxide units per mole sorbitan trioleate, sorbitan trilaurate, ethoxylated sorbitan trilaurate with 5-30 mole ethylene oxide units per mole Sorbitan trilaurate and mixtures thereof.
  • the Polyglycerinesteranteil may be composed of at least 75% di-, tri- and Tetraglycerinestern.
  • the polyglycerol ester is formed from the group of polyglycerol esters with fatty acids containing 10-25 carbon atoms, derivatives of polyglyceric acids with fatty acids containing 10-25 carbon atoms, polyglycerol polyricinoleate, derivatives of polyglycerol polyricinoleate and mixtures thereof ,
  • the formulation contains as emulsifier a) sorbitan tristearate or ethoxylated sorbitan tristearate with 5-30 mol ethylene oxide units per mole sorbitan tristearate, b) polyglycerol polyricinoleate and c) sorbitan monolaurate and d) ethoxylated sorbitan monolaurate with 5-30 mol ethylene oxide units per mole sorbitan monolaurate and e ) Sorbitan monooleate.
  • emulsifier a) sorbitan tristearate or ethoxylated sorbitan tristearate with 5-30 mol ethylene oxide units per mole sorbitan tristearate, b) polyglycerol polyricinoleate and c) sorbitan monolaurate and d) ethoxylated sorbitan monolaurate with 5-30 mol ethylene oxide units per mole sorbitan monolaurate and e ) Sorbit
  • the emulsifier is present as a mixture of at least two emulsifiers, based on the weight of the formulation, 1 to 15% by weight of ethoxylated sorbitan tristearate with 5 to 30 mol of ethylene oxide units per mole of sorbitan tristearate in the mixture of emulsifiers and / or from 1 to 15% by weight of polyglycerol polyricinoleate and / or polyricinoleate in the mixture of emulsifiers.
  • the emulsifier is present as a mixture of at least two emulsifiers, based on the weight of the formulation 1 to 15 wt .-% ethoxylated sorbitan monolaurate with 5 to 30 moles of ethylene oxide per mole of sorbitan monolaurate in the mixture of emulsifiers and / or based on the weight of the formulation contains from 1 to 15% by weight of sorbitan monooleate with from 5 to 30 mol of ethylene oxide units per mole of sorbitan monooleate in the mixture of emulsifiers.
  • the formulation of the invention contains 30-80 wt.% Of the mineral oil, preferably 40-80 wt .-%, particularly preferably 45-75 wt .-% and most preferably 55-72 wt.% Of the mineral oil.
  • the formulation preferably contains 15-60% by weight of the emulsifier, more preferably 20-60% by weight, particularly preferably 25-55% by weight of the emulsifier.
  • the formulation according to the invention is a water-in-oil or an oil-in-water emulsion.
  • the formulation according to the invention is applied after the spinning process in emulsion form on the surface of the threads, which are processed into filters for tobacco products.
  • the mineral oil remains on the surface of the threads or the dew.
  • the filaments used contain cellulose acetate containing on average 1.5 to 3 acetate groups per unit cellulose.
  • filaments also means fibers which can be produced by the process described here.
  • filters for tobacco products can be produced filters for tobacco products. It is preferred that the filters are cigarette filters. In all operations, the applied emulsion remains on the threads and thus on the rope. Thus, to a certain extent, the emulsion is still present in the filters for tobacco products and the tobacco itself.
  • the emulsion according to the invention is illustrated by the following examples, but without being limited to these examples.
  • Formulation 1 [% by weight] Formulation 2 [% by weight]
  • Mineral oil Primol ® 352 1 64,50 60,00 Sorbitan monolaurate + 20 EO 2 12,80 11,60 sorbitan 8.20 13,00 Sorbitan tristearate + 20 EO 2 - 4.40 Polyglycerol polyricinoleate 3.10 3.00 sorbitan 5.77 - water rest rest 1
  • Primol ® 352 is a high viscosity mineral oil of ESSO AG viscosity according to ASTM D 445: 71 mm 2 / s at 40 ° C, 9.0 mm 2 / s at 100 ° C 2 + 20 EO means 20 moles of ethylene oxide units per mole of ester
  • Formulations 1 and 2 from Table 1 both contain the combination according to the invention of a mineral oil having a viscosity of at least 8.5 mm 2 / s at 100 ° C. and the emulsifier according to the invention.
  • the emulsions can be prepared by standard methods.
  • Primol 352 is initially charged at room temperature and, while stirring continuously, the raw materials are added in the order of sorbitan monolaurate, sorbitan monolaurate + 20 EO, sorbitan monooleate, polyglycerol polyricinoleate and water.
  • Formulation 1 is stirred for a further 30 minutes.
  • primer 352 heated to 50 ° C. is initially charged in a stirrer.
  • the further raw materials are added in the order of sorbitan monolaurate, sorbitan monolaurate + 20 EO, sorbitan tristearate + 20 EO, polyglycerol polyricinoleate and water. After stirring for 30 minutes at 50 ° C, the formulation is allowed to cool to room temperature and stirred at this temperature for a further 30 minutes.
  • Both formulations are used to produce cellulose acetate filaments by the solvent spinning method. In this case, no negative influence of the formulations according to the invention was shown in the production of the threads.
  • Formulation 1 and Formulation 2 show storage stability at 23 ° C and five days, comparable to the formulations commonly used, and no increase in clouding of the emulsion due to shear forces occurred during processing of the filaments into filters. Both formulations behaved similarly to the commonly used formulations.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Edible Oils And Fats (AREA)
  • Colloid Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Tobacco Products (AREA)
  • Fats And Perfumes (AREA)

Claims (14)

  1. Formulation pour un usage comme lubrifiant dans la fabrication de fils, contenant :
    a) 30 à 80 % en poids d'une huile minérale présentant une viscosité d'au moins 8,5 mm2/s à 100 °C, et
    b) 11 à 60 % en poids d'un émulsionnant choisi parmi des monoesters de sorbitanne, des dérivés de monoesters de sorbitanne, des diesters de sorbitanne, des dérivés de diesters de sorbitanne, des triesters de sorbitanne, des dérivés de triesters de sorbitanne, des esters de polyglycérol, des dérivés d'esters de polyglycérol, un polyricinoléate, des dérivés de polyricinoléate et des mélanges de ceux-ci ; et caractérisée en outre en ce que
    la formulation est une émulsion eau dans l'huile ou une émulsion huile dans l'eau.
  2. Formulation selon la revendication 1, caractérisée en ce que le triester de sorbitanne est choisi dans le groupe constitué d'un triester de sorbitanne et d'acides gras qui contiennent 10 à 25 atomes de carbone, d'un triester de sorbitanne éthoxylé et d'acides gras qui contiennent 10 à 25 atomes de carbone et qui contiennent 5 à 30 moles d'unités oxyde d'éthylène par mole de triester de sorbitanne, et de mélanges de ceux-ci.
  3. Formulation selon la revendication 2, caractérisée en ce que le triester de sorbitanne est choisi dans le groupe constitué du tristéarate de sorbitanne, du tristéarate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de tristéarate de sorbitanne, du trioléate de sorbitanne, du trioléate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de trioléate de sorbitanne, du trilaurate de sorbitanne, du trilaurate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de trilaurate de sorbitanne et de mélanges de ceux-ci.
  4. Formulation selon la revendication 1, caractérisée en ce que l'ester de polyglycérol est choisi dans le groupe constitué d'esters de polyglycérol et d'acides gras qui contiennent 10 à 25 atomes de carbone, de dérivés d'esters de polyglycérol et d'acides gras qui contiennent 10 à 25 atomes de carbone, de polyricinoléate de polyglycérol, de dérivés de polyricinoléate de polyglycérol et de mélanges de ceux-ci.
  5. Formulation selon l'une quelconque ou plusieurs des revendications 1 à 4, caractérisée en ce que l'émulsion contient 15 à 60 % en poids de l'émulsionnant.
  6. Formulation selon l'une quelconque ou plusieurs des revendications 1 à 5, caractérisée en ce que la formulation contient, comme émulsionnant, les composants suivants :
    a) du tristéarate de sorbitanne ou du tristéarate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de tristéarate de sorbitanne,
    b) du polyricinoléate de polyglycérol,
    c) du monolaurate de sorbitanne,
    d) du monolaurate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de monolaurate de sorbitanne, et
    e) du mono-oléate de sorbitanne.
  7. Formulation selon l'une quelconque ou plusieurs des revendications 1 à 6, caractérisée en ce que, lorsque l'émulsionnant se présente sous la forme d'un mélange d'au moins deux émulsionnants, le mélange d'émulsionnants contient, par rapport au poids de la formulation, 1 à 15% en poids de tristéarate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de tristéarate de sorbitanne et/ou le mélange d'émulsionnants contient, par rapport au poids de la formulation, 1 à 15 % en poids de polyricinoléate de polyglycérol et/ou de polyricinoléate.
  8. Formulation selon l'une quelconque ou plusieurs des revendications 1 à 7, caractérisée en ce que, lorsque l'émulsionnant se présente sous la forme d'un mélange d'au moins deux émulsionnants, le mélange d'émulsionnants contient, par rapport au poids de la formulation, 1 à 15 % en poids de monolaurate de sorbitanne éthoxylé avec 5 à 30 moles d'unités oxyde d'éthylène par mole de monolaurate de sorbitanne et/ou le mélange d'émulsionnants contient, par rapport au poids de la formulation, 1 à 15 % en poids de mono-oléate de sorbitanne avec 5 à 30 moles d'unités oxyde d'éthylène par mole de mono-oléate de sorbitanne.
  9. Formulation selon la revendication 1, caractérisée en ce que l'huile minérale présente une viscosité de 8,5 à 1000 mm2/s à 100 °C.
  10. Fils pouvant être obtenus par un procédé de filage, dans lequel les fils sont préparés, après le filage, avec la formulation selon l'une quelconque ou plusieurs des revendications 1 à 9 comme lubrifiant, par application à la surface des fils.
  11. Fils selon la revendication 10, caractérisés en ce que les fils contiennent de l'acétate de cellulose comprenant, en moyenne, 1,5 à 3 groupements acétate par unité de cellulose.
  12. Filtre de cigarette, contenant des fils selon la revendication 10 ou 11.
  13. Utilisation de la formulation selon l'une quelconque ou plusieurs des revendications 1 à 9, comme lubrifiant dans la fabrication de fils pour des filtres destinés à des produits de tabac.
  14. Utilisation de la formulation selon la revendication 13, caractérisée en ce que l'on emploie les fils pour fabriquer des filtres de cigarettes.
EP03732455A 2002-07-11 2003-05-24 Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac Expired - Lifetime EP1530657B1 (fr)

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Application Number Priority Date Filing Date Title
EP03732455A EP1530657B1 (fr) 2002-07-11 2003-05-24 Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP02015405 2002-07-11
EP02015405A EP1380684A1 (fr) 2002-07-11 2002-07-11 Composition d'une huile minérale à haute viscosité pour la production de filtres pour articles à base de tabac
PCT/EP2003/005440 WO2004007831A1 (fr) 2002-07-11 2003-05-24 Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac
EP03732455A EP1530657B1 (fr) 2002-07-11 2003-05-24 Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac

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EP1530657A1 EP1530657A1 (fr) 2005-05-18
EP1530657B1 true EP1530657B1 (fr) 2010-04-28

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EP03732455A Expired - Lifetime EP1530657B1 (fr) 2002-07-11 2003-05-24 Formulation d'une huile minerale a viscosite elevee pour la realisation de filtres pour produits du tabac

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EP02015405A Withdrawn EP1380684A1 (fr) 2002-07-11 2002-07-11 Composition d'une huile minérale à haute viscosité pour la production de filtres pour articles à base de tabac

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Country Link
US (1) US7153447B2 (fr)
EP (2) EP1380684A1 (fr)
AT (1) ATE466130T1 (fr)
AU (1) AU2003238389A1 (fr)
DE (1) DE50312667D1 (fr)
WO (1) WO2004007831A1 (fr)

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US7585442B2 (en) 2004-06-25 2009-09-08 Celanese Acetate, Llc Process for making cellulose acetate tow
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GB0517551D0 (en) * 2005-08-27 2005-10-05 Acetate Products Ltd Process for making filter tow
US8336557B2 (en) * 2007-11-28 2012-12-25 Philip Morris Usa Inc. Smokeless compressed tobacco product for oral consumption
US8685904B2 (en) 2008-06-20 2014-04-01 3M Innovative Properties Company Aqueous lubricant emulsion for medical or apparatus and a method of washing
GB201400990D0 (en) * 2014-01-21 2014-03-05 British American Tobacco Co Filter materials and filters made therefrom
EP3409829B1 (fr) * 2017-05-30 2020-08-12 Rhodia Acetow GmbH Composition comprenant des hydrocarbures, des émulsifiants et de l'eau, son utilisation et produits comprenant une telle composition

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Also Published As

Publication number Publication date
DE50312667D1 (de) 2010-06-10
US20040007687A1 (en) 2004-01-15
WO2004007831A1 (fr) 2004-01-22
EP1380684A1 (fr) 2004-01-14
AU2003238389A1 (en) 2004-02-02
EP1530657A1 (fr) 2005-05-18
ATE466130T1 (de) 2010-05-15
US7153447B2 (en) 2006-12-26

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