EP1589145A1 - Chiffons au polyoléfine - Google Patents

Chiffons au polyoléfine Download PDF

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Publication number
EP1589145A1
EP1589145A1 EP20050008304 EP05008304A EP1589145A1 EP 1589145 A1 EP1589145 A1 EP 1589145A1 EP 20050008304 EP20050008304 EP 20050008304 EP 05008304 A EP05008304 A EP 05008304A EP 1589145 A1 EP1589145 A1 EP 1589145A1
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EP
European Patent Office
Prior art keywords
wipes
acid
impregnation
alcohol
nonwovens
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.)
Withdrawn
Application number
EP20050008304
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German (de)
English (en)
Inventor
Christine Wild
Ulrich Issberner
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.)
Cognis IP Management GmbH
Original Assignee
Cognis Deutschland GmbH and Co KG
Cognis IP Management GmbH
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 Cognis Deutschland GmbH and Co KG, Cognis IP Management GmbH filed Critical Cognis Deutschland GmbH and Co KG
Publication of EP1589145A1 publication Critical patent/EP1589145A1/fr
Withdrawn legal-status Critical Current

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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
    • D06M13/165Ethers
    • D06M13/17Polyoxyalkyleneglycol ethers
    • 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
    • D06M13/144Alcohols; Metal alcoholates
    • 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
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/207Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
    • D06M13/217Polyoxyalkyleneglycol ethers with a terminal carboxyl group; Anhydrides, halides or salts thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2484Coating or impregnation is water absorbency-increasing or hydrophilicity-increasing or hydrophilicity-imparting
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2861Coated or impregnated synthetic organic fiber fabric
    • Y10T442/291Coated or impregnated polyolefin fiber fabric
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60Nonwoven fabric [i.e., nonwoven strand or fiber material]

Definitions

  • the invention is in the field of textile technology and relates to polyolefin inconvenience Wipes permanently hydrophilized by hydrophilic additives and subsequently an impregnation with spin finishes and / or aqueous solutions and / or emulsions are subjected. Furthermore, the use becomes permanently hydrophilic polyolefin inconveniencer materials and the corresponding method for the preparation of Wipes described.
  • Wipes that are used in the personal hygiene sector such as facial tissues, cosmetic pads, baby wipes, personal hygiene and household and industrial wipes are mostly used in aqueous medium and require good wettability with polar liquids.
  • hydrophilic fibers such as cellulose fibers, such as viscose or pulp, or their combination with polyester or polypropylene, are mostly used for the production of wipes.
  • the web formation takes place via an airlaid or carding process with subsequent chemical, thermal or mechanical bonding.
  • These so-called staple fiber webs often have insufficient abrasion resistance. Acceptable abrasion resistance must be paid for with pure staple fiber webs with a reduced sensor technology. It is therefore desirable to produce nonwovens which were either produced exclusively from a spunbonded nonwoven or which have a composite structure in which at least one layer consists of a spunbonded nonwoven.
  • Spunbonded nonwovens are generally made of thermoplastics (polyesters, polyolefins) produced. These can be obtained without the addition of hydrophilic additives due to the insufficient water absorption of the pure polymers are not used for wipes, where absorption of hydrophilic substances or aqueous emulsions is desired ..
  • Such additives are usually together with a polyolefin granules to a Pre-mixture (masterbatch) processed, which then as such the polymer granules added before processing to the fiber or other end products and then is extruded.
  • masterbatch Pre-mixture
  • the additives described in WO 02/092891 can also be used directly be dosed during the extrusion process in the extrusion plant.
  • Object of the present invention is versatile wipes available despite advantageous production, advantageous application, cleaning and and care properties.
  • the present invention relates to wipes obtainable by permanent Hydrophilization of polyolefin-containing materials with a hydrophilic additive and subsequent impregnation of the nonwovens made from these materials with spin finishes and / or aqueous solutions and / or emulsions.
  • the wipes of the invention on the one hand a better release of the solutions and emulsions with which they are impregnated, which is noticeable by a more pleasant skin feel after the application power.
  • an impregnation with an emulsion (O / W or W / O) 2-phase cleaning wipes can be produced, which are initially a cooling / cleansing Feeling on the skin produce a creamy effect on the last Leave skin behind. This effect is not only with spunbonded nonwovens but also with carded ones Nonwovens containing hydrophilized polypropylene staple fibers can be observed.
  • the wipes of the invention are characterized by a cheaper production, higher production speed and by their lower weight at a very high degree of softness.
  • the softness is achieved by the addition of hydrophilic additives in polypropylene.
  • the abrasion-resistant nonwovens additionally improve the cleaning effect, since a higher pressure during use is possible in comparison to pure staple fiber webs.
  • the pure hydrophilized polyolefin nonwovens can be recycled by recycling, as they are not possible when combined with cellulose fibers.
  • the low nonwoven weight and the softness of the nonwovens produced with hydrophilic additives has a favorable effect on this "memory effect" in comparison to pure PES / viscose mixtures.
  • the wipes can be used in personal hygiene areas, such as facial tissues, Cosmetic pads, baby wipes, body hygiene wipes, but also as cleaning wipes for the household and for the industrial sector. It can be dry Wipes or so-called wet wipes.
  • Hydrophilic polyolefin nonwovens absorb hydrophilic solvents such as water, alcohols, glycols, in almost the same way Mass such as hydrophobic substances, such as mineral oils ester oils and silicone brine. This attribute is particularly important for industrial towels, as here is a good Absorption of hydrophilic and hydrophobic substances is desired.
  • the polyolefin-containing materials are doing by the usual methods of the state The technology internally permanently hydrophilized and the towels made from it subsequently impregnated.
  • the impregnation is done by spraying, dipping, printing or roller application, wherein a multiple impregnation with the same or different formulations is possible.
  • the solutions / emulsions usually used have proven by spin finishes.
  • Typical means of initial impregnation are spin finishes consisting of surfactants and oils in aqueous solution / emulsion a surface tension of less than 45 dynes / cm at 20 degrees at application concentration such as Stantex® S 6327 (Cognis Dusseldorf), Stantex® S 6051-1 (Cognis Dusseldorf). This Clearimstorygnierung leads to a uniformity the hydrophilicity and absorption on the web and has an advantageous effect on the distribution of the secondary impregnation.
  • the second impregnation agents are solutions / emulsions consisting of surfactants, when it comes mainly to towels for household and industrial cleaning purposes or surfactants and / or skin care substances for the field of personal hygiene.
  • the emulsions have been found to be particularly water-based systems with care components such as Belsoft Care® 6600 (Cognis Dusseldorf), or else so-called PIT (phase invasion temperature) emulsions, such as Emulgade® CM (Cognis Dusseldorf).
  • Suitable hydrophilic additives are those already known from the prior art Reaction products of 1 part of polyethylene glycol with 2 parts of fatty acids, preferably Fatty acids with 10 to 12 C atoms or their derivatives for permanent hydrophilization polyolefin-containing materials.
  • additives which follow the general formula (I), ABCBA in which A is in each case a radical R-COO, where R is a saturated, branched or unbranched alkyl radical having 7 to 21 C atoms, B is in each case a group (C n H 2n O) k, where n is an integer from 2 to 4 and k may have the values from 1 to 15 and C is a linear or branched alkylene radical having at least 2 and at most 6 C atoms which may optionally also be interrupted by oxygen atoms.
  • the index k here refers to the single group B and does not indicate the total number of groups B in the molecule. The index k varies due to the different, technically induced degrees of alkoxylation of the individual molecules and can therefore also be odd.
  • the compounds of general formula (I) are, for example, by reaction of diols, e.g. Polyalkylene glycols and alkoxides and with saturated fatty acids receive.
  • diols e.g. Polyalkylene glycols and alkoxides and with saturated fatty acids receive.
  • diols with 2 to 6 carbon atoms must be present, which the Forming block C of the additives of the invention, as well as ethylene, propylene and / or Butylene oxide, which form the groups B in the compounds of the invention.
  • the free hydroxyl groups of the alkoxides are saturated with fatty acids having 8 to 22 carbon atoms terminated.
  • the diols are preferably selected from the group consisting of 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol and 1,4-butanediol. In principle, it is also possible to use mixtures of the diols, it being advantageous to select only one diol for the reaction.
  • compounds of the formula (I) with different groups C are obtained.
  • this divalent group is a CH 2 -CH 2 , CH 2 -CH (CH 3 ), CH 2 -CH 2 -CH 2 or (CH 2 ) 4 group.
  • the group C may also be advantageous for the group C to contain one or more oxygen atoms. This preferably applies to an additive which is started on the basis of diethylene glycol, dipropylene glycol or similar ether compounds.
  • C in the formula (I) is then a divalent group CH 2 -CH 2 -O-CH 2 -CH 2 -O or (CH 2 ) 3 -O- (CH 2 ) 3 -O.
  • the alkoxides are selected from the group of ethylene oxide, propylene oxide and butylene oxide, where any mixtures are possible here. Be different Alkoxides can be alkoxylated both blockwise and randomized respectively.
  • the number of alkoxide units in the compounds of formula (I) varies in the range of a total of 2 to 30, so that k can each take on the value 1 to 15.
  • Preference is given to those compounds of the formula (I) in which k in each case represents the numbers 2 to 15 and in particular 4 to 10 and very particularly preferably 10 or 5 stands.
  • Farther preference is given to those compounds of the formula (I) which also contain ethylene oxide units
  • Group B contain, preferably only ethylene oxide units.
  • Suitable saturated fatty acids which can form the group A of the compounds according to the invention are preferably selected from the group of octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid heptadecanoic acid and octadecanoic acid, as well as nonadecanoic acid, eicosanoic acid and heneicosanoic acid as well as docosanoic acid.
  • Preferred compounds which are suitable as additives for the purposes of the present invention are those of the formula (I) in which R is a linear alkyl radical having 9 C atoms, k in each case has the value 5, n is 2 and C is a radical CH 2 -CH (CH 3 ) or in which R is a linear alkyl radical having 11 C atoms, k has the value 5, n is 2 and C is a radical CH 2 -CH 2 (CH 3 ).
  • A is a radical R-COO, wherein R is a saturated, branched or unbranched alkyl radical having 7 to 21 carbon atoms, B each is a group C.
  • a preferred additive of formula (I) comprises as part C a diethylene glycol residue, as groups B are 5 to 7 parts EO and 2 to 4 parts PO, and the radical R is in each case a lauric acid residue.
  • the additives according to the invention can be used alone or in mixtures with one another be used.
  • other known from the prior art additives be added for polymer extrusion or production.
  • polystyrene resin With regard to the material containing polyolefins, all known today are suitable Polymer and copolymer types based on ethylene or propylene. Also Blends of pure polyolefins with copolymers are suitable in principle.
  • the hydrophilic additives in blends of polyolefins with other synthetic ones can be used or natural polymers, e.g. Cellulose, polylactic acid or hemp used to give the polyolefin fibers permanently hydrophilic properties.
  • poly (ethylene) such as HDPE (high density polyethylene), Low density polyethylene (LDPE), very low density polyethylene (VLDPE), LLDPE (linear low density polyethylene), MDPE (medium density polyethylene), UHMPE (ultra high molecular weight polyethylene), VPE (cross-linked polyethylene), HPPE (high pressure polyethylene);
  • Poly (propylene) such as isotactic polypropylene; syndiotactic polypropylene; Metallocene catalysed polypropylene, impact modified polypropylene, Random copolymers based on ethylene and propylene, block copolymers based on ethylene and propylene; EPM (poly [ethylene-co-propylene]); EPDM (poly [ethylene-co-propylene-co-conjugated Diene]).
  • homopolymers and copolymers based on ethylene and propylene is particularly preferred.
  • polyolefin as polyethylene
  • polypropylene in one another embodiment exclusively polypropylene
  • Copolymers based on ethylene and propylene in one another embodiment exclusively polypropylene
  • the additives used in polypropylene fibers preferably have a melt flow rate of greater than 10 to 1500 dg / min (measured at 230 ° C and 2.16 kg load) wherein fibers having, for example, 150 to 1200 or 20 to 25 or 400 to 1000 dg / min may be preferred.
  • the articles, preferably fibers or films, or fabrics such as nonwovens, from these fibers, the additives preferably contain in amounts of 0.1 to 5 wt .-%, preferably 0.5 to 5 wt .-% and in particular 1.0 to 3 wt .-% based on the Total weight of the items.
  • Nonwovens may be prepared by all methods of nonwoven production known in the art, as described, for example, in Ullmann's Encyclopedia of Industrial Chemistry, Vol. A 17, VCH Weinheim 1994, pages 572-581.
  • nonwovens Preference is given to nonwovens, either after the so-called “dry laid” - or Spunbond or spunbond process or melt-blow process (melt-spun) were manufactured.
  • the "dry laid” process is based on staple fibers, which are usually separated by carding into individual fibers and then using an aerodynamic or hydrodynamic process to unconsolidated nonwoven fabric become. This is then for example by a thermal treatment for finished fleece connected (the so-called “thermobonding”).
  • thermal treatment for finished fleece connected the so-called “thermobonding”
  • the synthetic Fibers either so far heated that their surface melts and the individual fibers be joined together at the contact points, or the fibers are with an additive coated, which melts during the heat treatment and so the individual Connecting fibers together. By cooling the connection is fixed.
  • an impregnation of hydrophilic Pololeolefin inconveniencer Nonwovens with O / W or W / O emulsions suitable.
  • hydrophilized polyolefin-containing nonwovens impregnated with an emulsion 2-phase cleaning wipes can be produced, which are initially a cooling / cleansing Feeling on the skin produce a creamy effect on the last Leave skin behind. This effect is not only with spunbonded nonwovens but also with carded ones Nonwovens containing hydrophilized polypropylene staple fibers can be observed.
  • One Another advantage of these cosmetic towels is the low bleeding in stacked Towels or fleeces. It was surprisingly found that at the Application of the hydrophilized polyolefin-containing cloths in combination with emulsions as impregnation, even during prolonged storage no decrease in the outer phase - oil or water - within the tissue or wipe stack.
  • the impregnation with emulsions can take place in the different process stages, i.e. during or immediately after the production of the webs with or without following Dry.
  • the impregnation can also be done in a second step after bonding before or during the conversion. Both impregnation methods can be combined become.
  • Suitable components (a) of the PIT emulsions are fatty acid alkyl esters of the formula (II) R 1 CO-OR 2 in which R 1 CO is a linear or branched, saturated or unsaturated acyl radical having 8 to 22, preferably 12 to 18 and in particular 14 to 16 carbon atoms and R 2 is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms , Typical examples are the esters of caprylic acid, isononanoic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures with caproic alcohol, caprylic alcohol, Ethylhexyl alcohol, capric alcohol, la
  • Wax esters are preferably used, ie fatty acid alkyl esters which have a plastic, but solid consistency at 20 ° C. and in total have from 24 to 48 carbon atoms.
  • Typical examples are myristyl myristate, cetearyl isononanoate, cetyl palmitate, cetyl stearate, stearyl palmitate, stearyl stearate and the like.
  • Fatty alcohols which can be used as component (b) are primary alcohols which preferably follow the formula (III), R 3 OH in which R 3 is a linear or branched alkyl and / or alkenyl radical having 8 to 22, preferably 12 to 18 and in particular 14 to 16 carbon atoms.
  • Typical examples are caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, elaidylstearyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures, for example in the high pressure hydrogenation of technical methyl esters Based on fats and oils or aldehydes from the Roelen oxo synthesis and as a monomer fraction in the dimerization of unsaturated fatty alcohols.
  • Alcohol polyglycol ethers which form component (c) are to be understood as meaning the adducts of ethylene oxide and / or propylene oxide with fatty alcohols of group (b) or oxo alcohols of the same chain length, which preferably follow formula (IV), R 4 O (CH 2 CHR 5 O) n H in which R 4 is a linear or branched alkyl and / or alkenyl radical having 8 to 22, preferably 12 to 18 carbon atoms and in particular 14 to 16, R 5 is hydrogen or methyl and n is a number from 1 to 50.
  • Typical examples are the adducts of an average of 1 to 50, preferably 5 to 40 and especially 10 to 20 moles of ethylene oxide with caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol , Erucylalkohol and brassidyl alcohol and their technical mixtures, for example, in the high pressure hydrogenation of technical methyl esters based on fats and oils or aldehydes from the Roelen oxo synthesis and as a monomer fraction in the dimerization of unsaturated fatty alcohols incurred.
  • Preferred are adducts of 10 to 20 moles of ethylene oxide with technical fatty alcohols having 16 to 18 carbon atoms, such as cetearyl alcohol or tallow fatty alcohol
  • the mixtures contain partial glycerides which follow formula (V), HIGH 2 CH (OH) CH 2 OCOR 6 in which R 6 CO is a linear or branched, saturated or unsaturated acyl radical having 8 to 22, preferably 12 to 18 and in particular 14 to 16 carbon atoms.
  • the partial glycerides ie monoglycerides, diglycerides and technical mixtures thereof, may still contain small amounts of triglycerides as a result of the preparation.
  • Typical examples are mono- and / or diglycerides based on caprylic, capric, lauric, palmitic, palmitic, stearic, isostearic, oleic, elaidic, petroselic, elaeostearic, arachidic, gadoleic, behenic and erucic acid, and technical mixtures thereof.
  • technical Palmitin Textreglyceride, Stearinklareglyceride, Isostearinklareglyceride, and / or Behenkladreglyceride be used which have a Monoglyceridanteil in the range of 50 to 95, preferably 60 to 90 wt .-%.
  • the preferred emulsions contain 5 to 50 wt .-% of a melting in the range of 25 to 37 ° C component a) selected from the group of paraffins, fatty acid esters, polyhydroxy fatty acid esters, fatty alcohols, alkoxylated fatty acid esters, alkoxylated fatty alcohols and mixtures of these compounds and 5 to 50 wt.
  • the component a) can be selected from a multiplicity of those known to the person skilled in the art Compounds, wherein it is essential that the melting point here in the range of 25 to Max. 37 ° C must lie.
  • certain paraffins but also fatty acid esters and in particular fatty alcohols are used.
  • the paraffins are suitable preferably semi-solid paraffins such as soft paraffin, preferably petrolatum.
  • suitable Fatty alcohols are, for example, dodecanol or ricinol alcohol to a representative of to name unsaturated fatty alcohols.
  • Particularly suitable in the context of the present invention is the use of glycerides, here preferably the mixtures of partial and Triglycerides, which have the desired melting point of 25 to 37 ° C. have to.
  • Particularly preferred here are mixtures of glycerides of fatty acids with 8 to 18 C atoms.
  • Glycerides provide mono-di- and / or triesters of glycerol with fatty acids, namely, for example Caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, Isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, Oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, Arachic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures
  • Typical examples are lauric acid monoglyceride, lauric acid diglyceride, Coconut fatty acid monoglyceride, coconut fatty acid triglyceride, palmitic acid monoglyceride, Palmitic acid triglyceride, stearic acid monoglyceride,
  • emulsifier component b is the use of emulsifier component b).
  • glycerol partial esters with C 12 -C 21 fatty acids preferably the glycerol monolaurate.
  • polyglycerol poly-12-hydroxystearate is particularly preferred.
  • Polyol poly-12-hydroxystearates are known substances which are sold, for example, under the trademarks Dehymuls®, PWPH or Eumulgin® VL75 or Dehymuls® SP11 by Cognis Deutschland-GmbH & Co. KG.
  • the fabrics were impregnated according to Table 2 with Emulgade® CM (Cognis Dusseldorf) in amounts of 2.5 g / m 2 .
  • the wipes were then dried at 30 ° C for 30 minutes and then the soft touch was evaluated on a panel consisting of 6 experienced tests on a scale from (1) very soft to (4) low softness.
  • the results which represent averages of three series of experiments, are shown in Table 2.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Nonwoven Fabrics (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
EP20050008304 2004-04-24 2005-04-15 Chiffons au polyoléfine Withdrawn EP1589145A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004020083 2004-04-24
DE200410020083 DE102004020083A1 (de) 2004-04-24 2004-04-24 Polyolefinhaltige Wischtücher

Publications (1)

Publication Number Publication Date
EP1589145A1 true EP1589145A1 (fr) 2005-10-26

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EP (1) EP1589145A1 (fr)
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US9181465B2 (en) 2009-11-20 2015-11-10 Kimberly-Clark Worldwide, Inc. Temperature change compositions and tissue products providing a cooling sensation
CN102670319A (zh) * 2011-03-14 2012-09-19 李兆桐 一次性口腔擦牙巾和刷牙套
CN102475514B (zh) * 2011-12-12 2013-07-10 浙江瑞邦日化有限公司 一种湿巾及其制备方法
US9394637B2 (en) 2012-12-13 2016-07-19 Jacob Holm & Sons Ag Method for production of a hydroentangled airlaid web and products obtained therefrom

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