EP0173528B1 - Wachsfreie Polyvinylalkohol enthaltende Schichtzusammensetzung - Google Patents

Wachsfreie Polyvinylalkohol enthaltende Schichtzusammensetzung Download PDF

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Publication number
EP0173528B1
EP0173528B1 EP85305877A EP85305877A EP0173528B1 EP 0173528 B1 EP0173528 B1 EP 0173528B1 EP 85305877 A EP85305877 A EP 85305877A EP 85305877 A EP85305877 A EP 85305877A EP 0173528 B1 EP0173528 B1 EP 0173528B1
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Prior art keywords
weight
ethylene oxide
amount
vinyl alcohol
average
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EP85305877A
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English (en)
French (fr)
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EP0173528A3 (en
EP0173528A2 (de
Inventor
Donald Arthur Vassallo
David William Zunker
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EIDP Inc
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EI Du Pont de Nemours and Co
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Classifications

    • 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
    • D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
    • 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

  • This invention relates to size compositions and more specifically it relates to polyvinyl alcohol based size compositions containing low ethylene oxide adduct additives.
  • Spun warp yarn must be sized with a water-soluble polymer which provides it with a protective surface coating; the latter is required during the weaving of the yarn into fabric.
  • a protective surface coating After weaving the greige fabric produced must be stripped of the protective coating by desizing before it can be subjected to various finishing operations and in particular to dyeing.
  • Sizes based on polyvinyl alcohol or combinations of polyvinyl alcohol and starch must generally be used with a wax additive present in the formulation to minimize drier drum sticking in the slasher during application of the size. These wax additives are difficult to remove from the greige fabric during desizing, often requiring extraction by special solvents as well as higher desize bath temperatures. As a consequence the finishing mill is faced with higher production costs due to greater process complexibility, higher energy costs and a higher percentage of second quality greige fabric.
  • polyvinyl alcohol-based sizing solution containing a small amount of quaternary ammonium salt or a quaternary imidazolinium salt is disclosed in U.S. Patent No. 4,383,063; these additives provide good operability in the absence of wax and result in fabric exhibiting improved finishing performance.
  • such formulations have the serious deficiency of frequently exhibiting a non- reproducible sizing performance; the latter is due to an erratic and unpredictable removal of the cationic additive by inter-action with anionic contaminants which tend to accumulate in the sizing solution.
  • the primary source of these anionic contaminants is the spun yarn being sized.
  • US ⁇ A ⁇ 4251403 discloses a size for monofilament yarns comprising polyvinyl alcohol urea and a mono- or di- saccharide such as sucrose.
  • a size comprising polyvinyl alcohol, urea and diethylpropanediol gave fair results with smooth polyester but, when applied to texturized polyester yarn, produced an undesirable quantity of shed when subjected to abrasion in the reciprocating reed test.
  • composition consisting essentially of (a) from 45.5 to 99.9% by weight of vinyl alcohol polymer selected from the group consisting of polyvinyl alcohol, vinyl alcohol/methyl methacrylate copolymer, and polyvinyl alcohol containing solubilizing comonomers other than methyl methacrylate, said vinyl alcohol polymer having a saponification number of from 1 to 160 and a 4 percent solution viscosity of from 3 to 70 MPa - at 20°C;
  • a concentrate of the low ethylene oxide adduct blended with vinyl alcohol polymer, a wax-free aqueous size solution comprising the composition of the present invention having a solids content of 2-20% by weight, process for sizing filament yarn with wax-free aqueous solution and sized yarn comprising spun yarn having a wax-free protective surface coating of the composition of the present invention.
  • the term "consisting essentially of” means that the named ingredients are essential, however, other ingredients which do not prevent the advantages of the present invention from being realized can also be included.
  • the vinyl alcohol polymer can have a saponification number (mg KOH to neutralize 1 g polymer) of from 1 to 160 and a 4 percent solution viscosity of from about 3 to about 70 MPa-s.
  • Suitable vinyl alcohol polymers include:
  • the nonionic additive is a low ethylene oxide adduct (containing an average ethylene oxide content of from 1 to 7 units) of a branched alcohol or a mixture of branched alcohols (having an average carbon content of from 8 to 18 units).
  • the preferred makeup of this additive is an adduct containing from 2 to 5 ethylene oxide units with a branched alcohol containing an average of from 10 to 15 carbon atoms.
  • the most preferred is one consisting of an average of 3 ethylene oxide units with a branched alcohol containing an average of 13 carbon atoms.
  • "Tergitol" 15-S-3 a product manufactured by Union Carbide, represents this most preferred additive.
  • the amount of vinyl alcohol polymer in the composition of the present invention is from 45.5 to 99.9 percent by weight.
  • the preferred range is from 63 to 99.8 percent and the most preferred range is from 72.7 to 99.6 percent.
  • the higher the polyvinyl alcohol content of the size the higher will be the weaving efficiency exhibited by the sized yarn.
  • size add-on requirements are reduced progressively as the polyvinyl alcohol content of the size is increased.
  • the amount of the nonionic additive of the present invention is from 0.1 to 3 percent by weight. 0.1 weight percent additive is necessary to give significant drier drum release, while greater than 3 weight percent may result in reduced weaving efficiencies.
  • a preferred range of additive is from 0.2 to 1.5 weight percent or, more preferably, 1 wt.% with which most of the benefits of the present invention can be achieved.
  • the most preferred concentration range of additive is from 0.4 to 0.8 weight percent; compositions containing this level of additive give the best balance of drum deposit performance, abrasion resistance and dye receptivity after desizing.
  • starch can be incorporated in the size compositions of the present invention in an amount of up to 49.9 weight percent. Up to this level of starch the benefits of the no-wax additive of the present invention are clearly evident.
  • the preferred starch limit is up to 33 weight percent, while the most preferred starch limit is up to 25 weight percent.
  • the effectiveness of the nonionic additive of the present invention approaches that observed with compositions containing vinyl alcohol polymer as the sole polymeric component.
  • a variety of types of starch and derived starch will function as optional additives in the composition of this invention.
  • Carboxymethyl cellulose can also be used as an optional ingredient in the composition of the present invention in an amount of up to 50 wt.%, preferably up to 33 wt.%, and most preferably up to 25 wt.%.
  • the combined weight of the starch and CMC ingredients should not exceed the weight of the vinyl alcohol polymer present in the composition.
  • Another optional additive is a low to medium molecular weight (200-800 number average) oligomer of ethylene oxide often added to vinyl alcohol polymer as a dedusting agent.
  • U.S. Patent No. 4,389,506 describes the use of 3 weight percent of "Carbowax”@ 600, a product of Union Carbide, as yielding the most preferred dust-free product. Concentrations up to 5 weight percent "Carbowax"° 600 result in only minor reductions in the benefits derived from the presence of the nonionic additive and represents the upper additive level recommended. A preferred upper limit is 3 weight percent while the most preferred upper limit of this type of additive is 1.5 weight percent. At the most preferred upper concentration the benefits derived from the nonionic additive can be almost fully realized.
  • additives can be auxiliary low ethylene oxide adducts (containing an average ethylene oxide content of from 1 to 7 units) of a linear alcohol or of a mixture of linear alcohols (having an average carbon content of from 8 to 18 units) or medium to high ethylene oxide adducts (containing an average ethylene oxide content of from 8 to 40 units) of linear or branched alcohols (having an average carbon content of from 8 to 18 units).
  • These additives can be present in the composition of the present invention in low concentrations, i.e. up to 1 wt. percent.
  • the aqueous size solution of the present invention will generally have a solids content of from 2 to 20 weight percent.
  • the preferred size bath solids content is from 5 to 15 weight percent while the most preferred formulation contains from 7 to 12 weight percent since this level of solids in most cases will provide sufficient size add-on to give the sized yarn adequate abrasion resistance.
  • the aqueous polyvinyl alcohol based size solution is considered to be unique because it does not contain a wax additive which must be present under normal mill conditions.
  • the aqueous size solution is prepared by slurrying polyvinyl alcohol with water at ambient temperature.
  • the nonionic additive along with any optional additives are then introduced.
  • the subsequent mixture is heated with stirring at about 77°C until complete solution has been achieved.
  • the size solution of the present invention can also be prepared directly from a blend of vinyl alcohol polymer with a low amount of the nonionic additive.
  • the polyvinyl alcohol/nonionic additive mixtures are produced by dry blending a variety of polyvinyl alcohol and the additive(s) under high intensity mixing conditions at a temperature at which the additive component(s) will be liquid(s). Moreover if more than one nonionic additive is used, the latter can be preblended and added as a single component.
  • the size solution of the present invention can also be produced by using a concentrate of the nonionic additive of the present invention in a vinyl alcohol polymer.
  • the concentrate consists essentially of from 45 to 90 percent by weight of vinyl alcohol polymer and from 10 to 55 percent by weight of the liquid, nonionic low ethylene oxide adduct additive of the present invention.
  • the concentrate can contain up to 45 percent by weight of starch, up to 45 percent by weight of Carbowax°, up to 45 percent by weight of carboxymethyl cellulose and up to 45 percent by weight of low ethylene oxide adduct of a linear alcohol or mixture of linear alcohols or medium to high ethylene oxide adduct of linear or branched alcohols.
  • the concentrate is used to produce the size composition of the present invention by adding it in the required amount to a preformed vinyl alcohol polymer solution.
  • Use of such a concentrate can provide a unique and surprising advantage. Normally when vinyl alcohol polymers are added even with vigorous agitation to hot aqueous solutions, the vinyl alcohol component fuses upon contact with the hot water and becomes very difficultly soluble.
  • the above described concentrate if it contains at least 30% by weight of the nonionic additive, is relatively easy to disperse when added directly to hot water.
  • the most preferred nonionic additive level is from 40% to 50%. Above 50% the vinyl alcohol polymer tends not to absorb all of the additive.
  • Use of the above described concentrate provides the highly desirable advantage of permitting rapid readjustments in the level of the nonionic additive in a given hot size bath to match specific mill requirement.
  • the above referred to concentrate contains from 45 to 70 percent by weight of vinyl alcohol polymer, from 30 to 55 percent by weight of nonionic additive, up to 20 percent by weight of starch, up to 20 percent by weight of Carbowax@, and up to 20 percent by weight of carboxymethyl cellulose.
  • the concentrate will contain from 50 to 60 percent by weight of vinyl alcohol polymer, from 40 to 50 percent by weight of nonionic additive, up to 5 percent by weight of starch, up to 5 percent by weight of Carbowax@ and up to 5 percent by weight of carboxymethyl cellulose.
  • the size is applied to the yarn web or sley using a slasher.
  • the latter is equipped with a heated size box containing the size formulation.
  • the unsized sley is sized by being drawn through the hot size solution, through squeeze rolls to remove excess size solution, over a series of heated drying drums, through a bust bar assembly to separate the sley into individual warp ends and finally onto a beam for collection.
  • the bust bar assembly to separate the sley into individual warp ends and finally onto a beam for collection.
  • the sized spun yarn produced using the size composition of the present invention has a wax-free protective surface coating and exhibits the unique property of providing excellent weaving performance despite the absence of wax in the vinyl alcohol polymer based size. Moreover the greige fabric produced being wax-free, is readily desizable under mild desize conditions yielding a desized fabric with excellent dye receptivity. Desizing is carried out by passing the sized greige fabric through an alkaline scour bath followed by several hot water (about 65-85°C) rinses. Fabric prepared with conventional wax-containing sizes requires much more stringent scouring and rinse conditions than are required with the size formulations of the present invention.
  • a high level of removal of the size components from the greige fabric is required prior to its processing in the finishing mill so as to permit efficient and reproducible dyeing as well as other finishing operations on the fabric. Both the no-wax sized yarn and the no-wax greige fabric produced from it are thus considered to be unique.
  • the no-wax size composition of the present invention is especially suited for use with polyester/cotton spun yarn blends. It is particularly useful for 65/35, 50/50 and 40/60 polyester/cotton spun yarn blends.
  • the size composition also has utility for 100% cotton spun yarns.
  • incorporación of the no-wax additive into vinyl alcohol polymer based size formulations permits the elimination of wax as an additive, making feasible the preparation of sized yarn exhibiting excellent slashing and weaving characteristics suitable for producing a variety of types of fabrics under typical weaving conditions (e.g. involving shuttle, airjet, rapier looms).
  • the derived fabrics, being wax-free, are characterized by easy size removal and the desized fabric exhibits superior dye receptivity.
  • Sizing solutions were prepared in a steam-jacketed kettle by adding the vinyl alcohol polymer to the requisite amount of ambient temperature water to obtain the desired size bath solids. The temperature of the slurry was brought to 77°C with stirring. Any additives to be tested in the formulation were added at this point.
  • the resulting size solution was used to size 24 ends of a polyester/cotton spun yarn using a "Callaway Slasher" Model 51 manufactured by West Point Foundry and Machine Co. operated at 10 meters/minute using pressure at the squeeze roll. After the yarn had been sized, the size add-on was measured by weight loss after extraction of the sized yarn with boiling water. Assessment of the performance of the size formulation during slashing as well as characterization of the sized yarn itself was carried out using the following test procedures.
  • the extent to which deposits form on the No. 1 drying drum in the slasher is related directly to the tendency of a given size formulation to cause sticking of the individual warp ends to the drying drums in the slasher.
  • the effectiveness of a release agent added to the size formulation to minimize yarn sticking in the drying section of the slasher can be measured accurately.
  • the amount of deposit collected provides a direct measure of a size formulation's performance, namely the greater the amount of drum deposit, the greater the tendency the formulation has to cause drying drum sticking.
  • PVA No. 2 a fully hydrolyzed vinyl alcohol/methyl acrylate copolymer having a 4% solution viscosity of 13.5 MPa.s and a saponification number of 40.
  • the actual drum deposit value observed and a rating proportionated against the PVA No. 2 value are given.
  • a rating of 0.200 or lower is considered necessary for operability under typical mill conditions of a 100% vinyl alcohol polymer size.
  • Abrasion resistance of the sized yarn is determined using a laboratory abrasion tester.
  • the test method employed consists of stringing 21 ends of sized yarn through a section of conventional weaving loom reed and applying controlled tension to each individual warp end. The reed is made to oscillate against the warp ends at one cycle/second and the number of cycles required to cause the breakage of each end is recorded. A second set of 21 ends is next tested in the same manner. The two sets of data obtained are then statistically averaged so as to give the number of cycles required to cause 50% breakage of the warp ends used in the test. This quantity in cycles is referred to as the F so rating for a given size formulation.
  • Abrasion resistance is highly dependent upon size add-on.
  • all F so data must be normalized to a given size add-on, namely, 10%. This is preferably done by obtaining F 50 values at six or more add-ons for a given size formulation and subjecting the resulting data to a linear regression analysis. All F so data reported in the characterization of the various examples cited have been treated in this manner. A maximum F 50 value was observed for size formulations prepared with PVA No. 1 (a fully hydrolyzed vinyl alcohol/methyl methacrylate copolymer having a 4% solution viscosity of 28 MPa.s and having a saponification number of 30). In all examples cited the actual F so value observed and a comparison rating with the PVA No.
  • Sized yarn to be used in this test is first heat set by passing it through an oven at 200°C with a holdup time of 45 seconds.
  • the heat-treated yarn is then desized under mild conditions consisting of soaking the yarn for 15 seconds at 55°C in a 0.5% Alkanol WXN (a modified sodium alkylaryl sulfonate supplied by E. I. du Pont de Nemours and Company) solution followed by rinsing the yarn for 45 seconds at 75°C three times.
  • Alkanol WXN a modified sodium alkylaryl sulfonate supplied by E. I. du Pont de Nemours and Company
  • Examples 1 and 2 which represent embodiments of the present invention, provided yarn having acceptable combinations of the three key performance features, comparative Examples 1 and 2 were unacceptable because in C-1 the drum deposit was too high, and in C-2 the dye receptivity was extremely poor.
  • the additive of the present invention provided the same advantages with compositions based on intermediate and partially hydrolyzed polyvinyl alcohols as was observed with the vinyl alcohol polymer compositions described in Examples 1, 2, 3 and 4.
  • the additive of the present invention provided beneficial effects when used with 50/50 vinyl alcohol polymer/starch blends in both drum deposit performance as well as in dye receptivity.
  • the additive reduced abrasion resistance to approximately the same extent as did the "Synchem" 110 wax additive.
  • Size formulations based on PVA No. 2 were prepared with several low ethylene oxide adducts of linear alcohols namely "Tergitol”® 25-L-3, “Alfonic” 1012-40 and “Alfonic” 1412-40 (Ex. C-11 to 13).
  • the hydrophobe is a linear alcohol in the "Alfonic” products and in “Tergitol”° 25-L-3 but is secondary alcohol in “Tergitol”® 15-S-3.
  • the above Table shows that "Alfonic” 1412-40 and “Tergitol”® 25-L-3 are an almost exact linear counterparts of "Tergitol”® 15-S-3.
  • the "Alfonic” products are supplied by Conoco and the "Tergitol”® products are supplied by Union Carbide.
  • Table VI shows the composition and properties of size formulations prepared with the above linear alcohol derived ethylene oxide adducts as well as with the additive of the present invention (Ex. 1).
  • Size formulations were prepared with PVA No. 2 modified with a range of "Tergitol”® 15-S products containing from 3 to 40 ethylene oxide units (i.e. "Tergitol”® 15-S-3 to "Tergitol”® 15-S-40).
  • the level of the "Tergitol”® additive was 0.4 wt.%, and 3.0% "Carbowax”® 600 was also present in the formulation. Included in Table VII are characterization data for these formulations and a formulation containing only the "Carbowax”® 600 additive.
  • Fabric samples which have been prepared from yarn sized with the size solution of the present invention have been compared with fabric samples identical in every respect except that the latter were prepared with yarn sized with a commercial PVA/tallow wax formulation. Both sets of samples were desized under mild conditions (e.g. 15 seconds soak at 55°C followed by three water rinses at 65°C).
  • the dye receptivity of the fabrics obtained with the size of the present invention exhibited eight times the dye receptivity of those obtained using the conventional wax-containing size. Moreover dye absorption by the former was regular and uniform whereas that exhibited by the latter was highly irregular and nonuniform.
  • the fabric used in Examples 11 and 21 consisted of a 65/35 polyester/cotton warp having a 36 singles cotton count, and filled with a 100% polyester weft so as to produce a 92/83 construction (ratio of warp threads to weft threads).
  • the warp yarn was sized with a size formulation containing 12.5% solids and contained a size add-on of 15.0%.
  • the size solution used in Example 11 corresponded exactly to that used in Example 2.
  • the size solution used in Comparative Example 21 was the same as that used in Comparative Example 2 except that it contained 10%. "Synchem" 110 wax instead of 8%.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Claims (17)

1. Zusammensetzung, welche im wesentlichen besteht aus
(a) 45,5 bis 99,9 Gew.-% Vinylalkoholpolymer, ausgewählt aus der aus Polyvinylalkohol, Vinylalkohol/ Methylmethacrylat-Copolymer und Polyvinylalkohol mit von Methylmethacrylat verschiedenen löslichmachenden Comonomeren bestehenden Gruppe, wobei das Vinylalkoholpolymer eine Verseifungszahl von 1 bis 160 und eine Viskosität in 4 %iger Lösung von 3 bis 70 MPa.s bei 20°C aufweist;
(b) 0,1 bis 3 Gew.-% flüssigem, nicht ionischem Ethylenoxidaddukt eines verzweigten Alkohols oder einer Mischung verzweigter Alkohole mit geringem Ethylenoxidgehalt, worin der durchschnittliche Ethylenoxidgehalt 1 bis 7 Einheiten beträgt und der Alkohol einen durchschnittlichen Kohlenstoffgehalt von 8 bis 18 Kohlenstoffatomen hat;
(c) 0 bis 49,9 Gew.-% Stärke;
(d) 0 bis 5 Gew.-% Ethylenoxidoligomer mit einem Molekulargewicht (Zahlenmittel) von 200 bis 800 und
(e) 0 bis 50 Gew.-% Carboxymethylcellulose;
(f) 0 bis 1 Gew.-% wenigstens eines Hilfs-Ethylenoxidaddukts, ausgewählt aus der aus Ethylenoxidaddukt mit geringem Ethylenoxidgehalt (mit einem durchschnittlichen Ethylenoxidgehalt von 1 bis 7 Einheiten) eines linearen Alkohols oder einer Mischung linearer Alkohole (mit einem durchschnittlichen Kohlenstoffgehalt von 8 bis 18 Einheiten) und Ethylenoxidaddukt mit mittlerem bis hohem Ethylenoxidgehalt (mit einem durchschnittlichen Ethylenoxidgehalt von 8 bis 40 Einheiten) eines linearen oder verzweigten Alkohols (mit einem durchschnittlichen Kohlenstoffgehalt von 8 bis 18 Einheiten) bestehenden Gruppe, mit der Maßgabe, daß das vereinigte Gewicht der Stärke und der Carboxymethylcellulose nicht das Gewicht an Vinylalkoholpolymer übersteigt.
2. Zusammensetzung nach Anspruch 1, worin das Vinylalkoholpolymer aus der aus vollhydrolysiertem Polyvinylalkohol mit einer Viskosität von 3 bis 70 MPa.s, vollhydrolysiertem Vinylalkohol/ Methylmethacrylat-Copolymer, das 3,5 bis 6 Gew.-% copolymerisiertes Methylmethacrylatcomonomer enthält, mit einer Viskosität von 3 bis 60 MPa.s, teilweise hydrolysiertem Polyvinylalkohol mit 4 bis 12 Mol- % Vinylacetat und einer Viskosität von 3 bis 60 MPa-s, Polyvinylalkohol, der aus der aus Methylacrylat und Methylwasserstoffmaleat bestehenden Gruppe ausgewählte löslichmachende Comonomere enthält, mit einer Viskosität von 3 bis 70 MPa-s sowie Mischungen dieser Vinylalkoholpolymere bestehenden Gruppe ausgewählt ist.
3. Zusammensetzung nach Anspruch 1 oder Anspruch 2, worin die Menge an Vinylalkoholpolymer etwa 63 bis etwa 99,8 Gew.-% ausmacht, die Ethylenoxidmenge 0,2 bis 1 Gew.-% ausmacht, die Stärkemenge 0 bis 33 Gew.-% ausmacht, die Menge an Ethylenoxidoligomer 0 bis 3 Gew.-% ausmacht, die Menge an Carboxymethylcellulose 0 bis 33 Gew.-% ausmacht und worin das Ethylenoxidaddukt einen durchschnittlichen Ethylenoxidgehalt von 2 bis 5 aufweist und der Alkohol einen durchschnittlichen Kohlenstoffgehalt von 10 bis 15 Kohlenstoffatomen hat.
4. Zusammensetzung nach Anspruch 1 oder Anspruch 2, worin die Menge an Vinylalkoholpolymer 72,7 bis 99,6 Gew.-% ausmacht, die Ethylenoxidadduktmenge 0,4 bis 0,8 Gew.-% ausmacht, die Stärkemenge 0 bis 25 Gew.-% ausmacht, die Menge an Ethylenoxidoligomer 0 bis 1,5 Gew.-% ausmacht, die Menge an Carboxymethylcellulose 0 bis 25 Gew.-% ausmacht und worin das Ethylenoxidaddukt einen durchschnittlichen Ethylenoxidgehalt von 3 aufweist und der Alkohol einen durchschnittlichen Kohlenstoffgehalt von 13 Kohlenstoffatomen hat.
5. Zusammensetzung, welche im wesentlichen besteht aus
(a) 45 bis 90 Gew.-% Vinylalkoholpolymer, ausgewählt aus der aus Polyvinylalkohol und Vinylalkohol/ Methylmethacrylat-Copolymer sowie Polyvinylalkohol mit von Methylmethacrylat verschiedenen löslichmachenden Comonomeren bestehenden Gruppe, wobei das Vinylalkoholpolymer eine Verseifungszahl von 1 bis 160 und eine Viskosität in 4 %iger Lösung von 3 bis 70 MPa-s bei 20°C hat;
(b) 10 bis 55 Gew.-% flüssigem nicht ionischem Ethylenoxidaddukt eines verzweigten Alkohols oder einer Mischung von verzweigten Alkoholen mit geringem Ethylenoxidgehalt, worin der durchschnittliche Ethylenoxidgehalt 1 bis 7 Einheiten beträgt und der Alkohol einen durchschnittlichen Kohlenstoffgehalt von 8 bis 18 Kohlenstoffatomen hat;
(c) 0 bis 45 Gew.-% Stärke;
(d) 0 bis 45 Gew.-% Ethylenoxidoligomer mit einem Molekulargewicht (Zahlenmittel) von 200 bis 800 und
(e) 0 bis 45 Gew.-% Carboxymethylcellulose;
(f) 0 bis 45 Gew.-% eines Hilfsethylenoxidaddukts, ausgewählt aus der aus Ethylenoxidaddukt mit geringem Ethylenoxidgehalt (mit einem durchschnittlichen Ethylenoxidgehalt von 1 bis 7 Einheiten) eines linearen Alkohols oder einer Mischung von linearen Alkoholen (mit einem durchschnittlichen Kohlenstoffgehalt von 8 bis 18 Einheiten) und Ethylenoxidaddukt mit mittlerem bis hohem Ethylenoxidgehalt (mit einem durchschnittlichen Ethylenoxidgehalt von 8 bis 40 Einheiten) eines linearen oder verzweigten Alkohols (mit einem durchschnittlichen Kohlenstoffgehalt von 8 bis 18 Einheiten) bestehenden Gruppe.
6. Zusammensetzung nach Anspruch 5, worin das Vinylalkoholpolymer aus der aus vollhydrolysiertem Polyvinylalkohol mit einer Viskosität von 3 bis 70 MPa-s, vollhydrolysiertem Vinylalkohol/ Methylmethacrylat-Copolymer, das 3,5 bis 6 Gew.-% copolymerisiertes Methylmethacrylatcomonomer enthält, mit einer Viskosität von 3 bis 60 MPa-s, teilweise hydrolysiertem Polyvinylalkohol mit 4 bis 12 Mol- % Vinylacetat und einer Viskosität von 3 bis 60 MPa-s, Polyvinylalkohol, der aus der aus Methylacrylat und Methylwasserstoffmaleat bestehenden Gruppe ausgewählte löslichmachende Comonomere enthält, mit einer Viskosität von 3 bis 70 MPa-s und Mischungen dieser Vinylalkoholpolymere bestehenden Gruppe ausgewählt ist.
7. Zusammensetzung nach Anspruch 5 oder Anspruch 6, worin die Menge an Vinylalkoholpolymer 45 bis 70 Gew.-% ausmacht, die Menge an Ethylenoxidaddukt 30 bis 55 Gew.-% ausmacht, die Stärkemenge 0 bis 20 Gew.-% ausmacht, die Menge an Ethylenoxidoligomer 0 bis 20 Gew.-% ausmacht, die Carboxymethylcellulosemenge 0 bis 20 Gew.-% ausmacht und worin das Ethylenoxidaddukt einen durchschnittlichen Ethylengehalt von 2 bis 5 aufweist und der Alkohol einen durchschnittlichen Kohlenstoffgehalt von 10 bis 15 Kohlenstoffatomen hat.
8. Zusammensetzung nach Anspruch 5 oder Anspruch 6, worin die Menge an Vinylalkoholpolymer 50 bis 60 Gew.-% ausmacht, die Menge an Ethylenoxidaddukt 40 bis 50 Gew.-% ausmacht, die Stärkemenge 0 bis 5 Gew.-% ausmacht, die Menge an Ethylenoxidoligomer 0 bis 5 Gew.-% ausmacht, die Carboxymethylcellulosemenge 0 bis 5 Gew.-% ausmacht und worin das Ethylenoxidaddukt einen durchschnittlichen Ethylenoxidgehalt von 3 aufweist und der Alkohol einen durchschnittlichen Kohlenstoffgehalt von 13 Kohlenstoffatomen hat.
9. Wachsfreie, wässrige Schlichtlösung, welche die Zusammensetzung eines der Ansprüche 1 bis 4 umfaßt, mit einem Feststoffgehalt von 2 bis 20 Gew.-%.
10. Wachsfreie, wässrige Schlichtlösung, welche die Zusammensetzung eines der Ansprüche 1 bis 4 umfaßt, mit einem Feststoffgehalt von 5 bis 15 Gew.-%.
11. Wachsfreie, wässrige Schlichtlösung, welche die Zusammensetzung eines der Ansprüche 1 bis 4 umfaßt, mit einem Feststoffgehalt von 7 bis 12 Gew.-%.
12. Verfahren zum Schlichten von versponnenem Garn mit einer wachsfreien wässrigen Lösung nach Anspruch 9, Anspruch 10 oder Anspruch 11.
13. Geschlichtetes Garn, welches gesponnenes Garn mit einer wachsfreien schützenden Oberflächenbeschichtung der Zusammensetzung eines der Ansprüche 1 bis 4 umfaßt.
14. Geschlichtetes Garn, welches gesponnenes Garn mit einem wachsfreien schützenden Oberflächenüberzug der Zusammensetzung eines der Ansprüche 1 bis 4 umfaßt, worin das Garn aus der aus gesponnenen Baumwolle- und Polyester/Baumwollegarnen bestehenden Gruppe ausgewählt ist.
15. Geschlichtetes Garn, welches ein gesponnenes Garn mit einem wachsfreien schützenden Oberflächenüberzug der Zusammensetzung eines der Ansprüche 1 bis 4 umfaßt, worin das Garn aus der aus gesponnenen 65/35-, 50/50- und 40/60-Polyester/Baumwollegarnen bestehenden Gruppe ausgewählt ist.
16. Gewebe, welches geschlichtetes Garn gemäß Anspruch 13, Anspruch 14 und Anspruch 15 umfaßt.
17. Verfahren zur Herstellung eines Gewebes, welches das Entschlichten des Gewebes nach Anspruch 16 dadurch umfaßt, daß es durch ein alkalisches Waschbad geführt und danach mehreren heißen Wasserspülungen unterworfen wird, wobei das Verfahren gegebenenfalls ferner die Durchführung wenigstens eines Appreturarbeitsgangs auf dem Gewebe umfaßt.
EP85305877A 1984-08-20 1985-08-19 Wachsfreie Polyvinylalkohol enthaltende Schichtzusammensetzung Expired - Lifetime EP0173528B1 (de)

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ES (2) ES8700863A1 (de)
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US4845140A (en) * 1986-07-07 1989-07-04 Air Products And Chemicals, Inc. Waxless polyvinyl alcohol size composition
CA1322825C (en) * 1986-07-07 1993-10-12 Finn L. Marten Waxless polyvinyl alcohol size composition
WO1991016490A1 (en) * 1990-04-12 1991-10-31 George Bodnar Fabric stabiliser
KR960009085B1 (ko) * 1990-08-29 1996-07-10 나까무라 히사오 섬유사이징제
JP3643485B2 (ja) * 1998-08-03 2005-04-27 東邦テナックス株式会社 チョップ用及び脱サイズ編織物用炭素繊維
CN105603750B (zh) * 2016-02-26 2018-05-15 苏州三和开泰花线织造有限公司 一种多功能环保通用型纺织浆料及其制备方法

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US3689314A (en) * 1970-02-24 1972-09-05 Kimberly Clark Co Method for fabricating improved flushable wrappers for absorbent pads and product obtained thereby
JPS525335B2 (de) * 1974-03-01 1977-02-12
JPS5488947A (en) * 1977-12-26 1979-07-14 Sanyo Chem Ind Ltd Novel w/o type emulsion of water-soluble vinyl polymer
DE2928307A1 (de) * 1979-07-13 1981-02-12 Hoechst Ag Klebemittel auf basis von polyvinylalkohol und seine verwendung

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ES8702540A1 (es) 1986-12-16
EP0173528A3 (en) 1987-12-16
KR920009254B1 (ko) 1992-10-15
ES8700863A1 (es) 1986-11-16
ZA856278B (en) 1987-03-25
HK89190A (en) 1990-11-09
EP0173528A2 (de) 1986-03-05
DE3576543D1 (de) 1990-04-19
ES546293A0 (es) 1986-11-16
MY100153A (en) 1990-02-22
KR860001913A (ko) 1986-03-24
CA1279141C (en) 1991-01-15
JPS6162549A (ja) 1986-03-31

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