Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/12—Chemical modification
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/12—Chemical modification
  • C08J7/123—Treatment by wave energy or particle radiation
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
  • B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L101/00—Compositions of unspecified macromolecular compounds
  • C08L101/12—Compositions of unspecified macromolecular compounds characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity
  • C08L101/14—Compositions of unspecified macromolecular compounds characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity the macromolecular compounds being water soluble or water swellable, e.g. aqueous gels
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2300/00—Characterised by the use of unspecified polymers
  • C08J2300/14—Water soluble or water swellable polymers, e.g. aqueous gels
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
  • C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
  • C08J2333/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical

Definitions

• the present invention relates to a process for the preparation of surface-modified water-absorbing polymer structures, the surface-modified water-absorbing polymer structures obtainable by this process, a composite comprising these surface-modified water-absorbing polymer structures and a substrate, a process for producing a composite, a composite obtainable by this process, chemical products include these surface-modified water-absorbing polymer structures or the composite as well as the use of the surface-modified, water-absorbing polymer structures or of the composite in chemical products.
• Superabsorbents are water-insoluble, crosslinked polymers which are capable of absorbing, and retaining under pressure, large quantities of aqueous fluids, in particular body fluids, preferably urine or blood, while swelling and forming hydrogels. In general, these diesstechniksaufhahmen amount to at least 10 times or even at least 100 times the dry weight of the superabsorbent or the superabsorbent compositions of water. These characteristics make these polymers mainly used in sanitary articles such as baby diapers, incontinence products or sanitary napkins.
• sanitary articles such as baby diapers, incontinence products or sanitary napkins.
• the production of superabsorbents is generally carried out by the radical polymerization of acid group-bearing, mostly partially neutralized monomers in the presence of crosslinkers.
• the choice of the monomer composition, the crosslinker and the polymerization conditions and the Processing conditions for the hydrogel obtained after the polymerization produce polymers with different absorption properties. Further possibilities are offered by the preparation of graft polymers, for example using chemically modified starch, cellulose and polyvinyl alcohol according to DE-OS 26 12 846.
• the absorption rate of the superabsorbent particles is a decisive criterion, which statements allows whether an absorbent core containing this superabsorber in high concentration, which has only a low proportion of fluff, is able to absorb it quickly on its first contact with liquids (so-called "first acquisition”).
• This "first aquisitiori 1" is dependent, inter alia, on the absorption rate of the superabsorbent material in the case of absorbent cores having a high superabsorber content.
• the surface of the superabsorbent can be increased by using smaller superabsorbent particles with a correspondingly higher surface to volume ratio.
• this has the consequence that the permeability and also other performance characteristics of the superabsorbent, such as retention, are reduced.
• an increase in the surface area of the superabsorbent particles can be achieved by, for example, pulverizing to produce superabsorbent particles having irregular shapes. It is also known, for example, from US Pat. No. 5,118,719 and US Pat. No.
• the object of the present invention was to provide a process for the production of superabsorbers, which makes it possible to increase the absorption rate of any selected precursor particles, preferably without any change in the particle size distribution.
• this method should be distinguished by the fact that the absorption rate of the superabsorber is increased by its use, the retention, ie the ability to retain absorbed liquid, but if possible not or at most only slightly reduced.
• an object of the invention was that the treatments of the surface of the superabsorbent particles behave at least neutral to the surface post-crosslinking with respect to the performance of the superabsorbent.
• the object of the present invention was to provide superabsorbents with an increased absorption rate which is higher than those of the prior art superabsorbers, which at the same time have the highest possible retention.
• this property profile of the superabsorbers should not change, or even only slightly, even during prolonged storage, for example over several weeks.
• step I) of the process according to the invention first of all a multiplicity of water-absorbing polymer structures are provided, wherein the term "plurality” as used herein preferably amounts to at least 1,000, more preferably at least 1,000,000 and most preferably at least 1,000 .000,000 is understood.
• Water-absorbing polymer structures which are preferred according to the invention are fibers, foams or particles, fibers and particles being preferred and particles being particularly preferred.
• polymer fibers are dimensioned so that they can be incorporated into or as yarn for textiles and also directly in textiles. It is preferred according to the invention that the polymer fibers have a length in the range of 1 to 500 mm, preferably 2 to 500 mm and more preferably 5 to 100 mm and a diameter in the range of 1 to 200 denier, preferably 3 to 100 denier and more preferably 5 own up to 60 deniers.
• Polymer particles which are preferred according to the invention are dimensioned so that they have an average particle size according to ERT 420.2-02 in the range from 10 to 3000 ⁇ m, preferably 20 to 2000 ⁇ m and particularly preferably 150 to 850 ⁇ m.
• the proportion of the polymer particles having a particle size in a range of 300 to 600 ⁇ at least 30 wt .-%, more preferably at least 40 wt .-% and most preferably at least 50 wt .-%, based on the total weight of the water-absorbing polymer particles is.
• the water-absorbing polymer structures provided in process step I) are based on partially neutralized, crosslinked acrylic acid.
• the water-absorbing polymer structures according to the invention are crosslinked polyacrylates which are at least 50 wt .-%, preferably at least 70 wt .-% and more preferably at least 90 wt .-%, respectively on the weight of the water-absorbing polymer structures, on carboxylate-carrying monomers.
• the water-absorbing polymer structures according to the invention are based on polymerized acrylic acid at least 50% by weight, preferably at least 70% by weight, based in each case on the weight of the water-absorbing polymer structures, which are preferably at least 20 mol%. %, more preferably at least 50 mol%, and more preferably in a range of 60 to 85 mol%> is neutralized.
• the water-absorbing polymer structures provided in process step I) are preferably obtainable by a process comprising the following process steps: i) free-radical polymerization of an aqueous monomer solution comprising a polymerizable, monoethylenically unsaturated, an acid group-carrying monomer (od) or a salt thereof, optionally one with the monomer (od) polymerizable, monoethylenically unsaturated monomer
• this treatment can be carried out before, during or even after the surface modification, wherein the surface modification and the treatment can also overlap in time.
• step i) is first an aqueous monomer solution comprising a polymerizable, monoethylenically unsaturated, an acid group-carrying monomer (od) or a salt thereof, optionally with the monomer (od) polymerizable, monoethylenically unsaturated monomer (a2), and optionally a crosslinker (a3) free-radically polymerized to obtain a Polymergeis.
• the monoethylenically unsaturated acid group-carrying monomers (od) may be partially or completely, preferably partially neutralized.
• the neutralization can be done partially or completely even after the polymerization.
• the neutralization can be carried out with alkali metal hydroxides, alkaline earth metal hydroxides, ammonia and also carbonates and bicarbonates.
• every other base is conceivable, which forms a water-soluble salt with the acid.
• a mixed neutralization with different bases is conceivable. Preference is given to neutralization with ammonia and alkali metal hydroxides, particularly preferably with sodium hydroxide and with ammonia.
• the free acid groups may predominate, so that this polymer structure has a pH value lying in the acidic range.
• This acidic water-absorbing polymer structure may be at least partially neutralized by a polymer structure having free basic groups, preferably amine groups, which is basic in comparison to the acidic polymer structure.
• MBIEA polymers represent a composition which, on the one hand, converts basic polymer structures capable of exchanging anions and, on the other hand, an acidic polymer structure which is acidic in comparison to the basic polymer structure
• the basic polymer structure has basic groups and is typically obtained by the polymerization of monomers bearing basic groups or groups that can be converted to basic groups Things about those which are primary, secondary or tertiary amines or the corresponding phosphines or at least two of the above functions All groups have.
• the group of monomers includes, in particular, ethyleneamine, allylamine, diallylamine, 4-aminobutene, alkyloxycycline, vinylformamide, 5-aminopentene, carbodiimide, formaldacin, melamine and the like, and also their secondary or tertiary amine derivatives.
• Preferred monoethylenically unsaturated acid group-bearing monomers (a1) are preferably those compounds which are mentioned in WO 2004/037903 A2, which is hereby incorporated by reference and thus as part of the disclosure, as ethylenically unsaturated acid group-containing monomers (al) .
• Particularly preferred monoethylenically unsaturated acid group-bearing monomers (a1) are acrylic acid and methacrylic acid, with acrylic acid being most preferred.
• monoethylenically unsaturated monomers (a2) copolymerizable with the monomers (a1) it is possible to use acrylamides, methacrylamides or vinylamides. More preferred co-monomers are, in particular, those which are in the-carrying monomers (al) are preferably those compounds which are mentioned as co-monomers ( ⁇ x2) in WO 2004/037903 A2.
• crosslinkers (a3) are preferably also those Used compounds which are mentioned in WO 2004/037903 A2 as crosslinker (a3). Among these crosslinkers, water-soluble crosslinkers are particularly preferred.
• the monomer solution may also contain water-soluble polymers (a4).
• Preferred water-soluble polymers comprising partially or fully saponified polyvinyl alcohol, polyvinylpyrrolidone, starch or starch derivatives, polyglycols or polyacrylic acid.
• the molecular weight of these polymers is not critical as long as they are water-soluble.
• Preferred water-soluble polymers are starch or starch derivatives or polyvinyl alcohol.
• the water-soluble polymers, preferably synthetic, such as polyvinyl alcohol can not only serve as a grafting base for the monomers to be polymerized. It is also conceivable to mix these water-soluble polymers only after the polymerization with the polymer gel or the already dried, water-absorbing polymer gel.
• the monomer solution may also contain auxiliaries (a5), these additives including, in particular, the initiators or complexing agents which may be required for the polymerization, such as, for example, EDTA.
• auxiliaries for the monomer solution are water, organic solvents or mixtures of water and organic solvents, wherein the choice of the solvent also depends in particular on the manner of the polymerization.
• the relative amount of monomers (a1) and (a2) and of crosslinkers (a3) and water-soluble polymers (a4) and auxiliaries (a5) in the monomer solution is preferably selected so that the water-absorbing polymer structure obtained in step iii) after drying. from 20 to 99.999% by weight, preferably from 55 to 98.99% by weight and more preferably from 70 to 98.79% by weight, based on the monomers (a1),
• Optimum values for the concentration, in particular of the monomers, crosslinkers and water-soluble polymers in the monomer solution can be determined by simple preliminary tests or else in the prior art, in particular US Pat. Nos. 4,286,082, DE-A-2,706,135, 4,076,663, DE-A 35 03 458, DE 40 20 780 C1, DE-A-42 44 548, DE-A-43 33 056 and DE-A-44 18 818 are taken.
• the solution polymerization is carried out in water as a solvent.
• the solution polymerization can be carried out continuously or batchwise. From the prior art, a wide range of possible variations in terms of reaction conditions such as temperatures, type and amount of initiators and the reaction solution can be found. Typical processes are described in the following patents: US Pat. No. 4,286,082, DE-A-27 06 135 A1, US Pat. No. 4,076,663, DE-A-35 03 458, DE 40 20 780 C1, DE-A-
• the polymerization is initiated as usual by an initiator.
• initiators for the initiation of the polymerization it is possible to use all initiators which form free radicals under the polymerization conditions and which are customarily used in the production of superabsorbers. It is also possible to initiate the polymerization by the action of electron beams on the polymerizable, aqueous mixture. However, the polymerization can also be initiated in the absence of initiators of the abovementioned type by the action of high-energy radiation in the presence of photoinitiators.
• Polymerization initiators may be contained or dispersed in the monomer solution. Suitable initiators are all compounds which decompose into free radicals and which are known to the person skilled in the art.
• redox system consisting of hydrogen peroxide, sodium peroxodisulfate and ascorbic acid is used to prepare the water-absorbing polymer structures.
• the inverse suspension and emulsion polymerization can also be used for the preparation of the water-absorbing polymer structures according to the invention.
• an aqueous, partially neutralized solution of the monomers (od) and (a2), optionally including the water-soluble polymers (a4) and auxiliaries (a5), is dispersed in a hydrophobic organic solvent with the aid of protective colloids and / or emulsifiers and initiated by radical initiators the polymerization.
• the crosslinkers (a3) are either dissolved in the monomer solution and are metered together with this or added separately and optionally during the polymerization.
• the addition of a water-soluble polymer (a4) takes place as a graft base over the monomer solution or by direct submission to the oil phase.
• the crosslinking can be effected by copolymerization of the polyfunctional crosslinker (a3) dissolved in the monomer solution and / or by reaction of suitable crosslinkers with functional groups of the polymer during the polymerization steps.
• the methods are described, for example, in the publications US 4,340,706, DE-A-37 13 601, DE-A-28 40 010 and WO-A-96/05234, the corresponding disclosure of which is hereby incorporated by reference.
• the polymer gel obtained in process step i) is optionally comminuted, this comminution taking place in particular when the polymerization is carried out by means of a solution polymerization.
• the comminution can be done by comminution devices known to those skilled in the art, such as a meat grinder.
• the optionally previously comminuted polymer gel is dried.
• the drying of the polymer gel is preferably carried out in suitable dryers or ovens.
• suitable dryers or ovens By way of example rotary kilns, fluidized bed dryers, plate dryers, paddle dryers or infrared dryers may be mentioned.
• the water-absorbing polymer structures obtained in process step iii) can in particular, if they were obtained by solution polymerization, still be ground and referred to at the outset
• Desired grain size are sieved.
• the grinding of the dried, water-absorbing polymer structures is preferably carried out in suitable mechanical comminution devices, such as a ball mill, while the screening can be carried out, for example, by using sieves of suitable mesh size.
• the optionally ground and sieved water-absorbing polymer structures can be surface-modified, wherein this surface modification preferably comprises a surface postcrosslinking and wherein this surface postcrosslinking in process step v) can in principle be carried out before, during or after the plasma treatment according to process step II) of the process according to the invention.
• the dried and optionally ground and screened (and possibly also already plasma-modified) water-absorbing polymer structures from process step iii), iv) or II) or the not yet dried, but preferably already comminuted polymer gel from Process step ii) is brought into contact with a preferably organic, chemical surface postcrosslinker.
• the postcrosslinker in particular if it is not liquid under the postcrosslinking conditions, preferably in the form of a fluid comprising the postcrosslinker and a solvent in contact with the water-absorbing polymer structure or the polymer gel.
• the solvents used are preferably water, water-miscible organic solvents such as, for example, methanol, ethanol, 1-propanol, 2-propanol or 1-butanol or mixtures of at least two of these solvents, water being the most preferred solvent.
• the postcrosslinker be contained in the fluid in an amount in a range of from 5 to 75% by weight, more preferably from 10 to 50% by weight, and most preferably from 15 to 40% by weight, based on the Total weight of the fluid is included.
• the bringing into contact of the water-absorbing polymer structure or the optionally comminuted polymer gel with the fluid containing the post-crosslinker is preferably carried out by good mixing of the fluid with the polymer structure or the polymer gel.
• Suitable mixing units for applying the fluid are z.
• the Patterson-Kelley mixer As the Patterson-Kelley mixer, DRAIS turbulence mixers, Lödigemischer, Ruberg mixer, screw mixers, plate mixers and fluidized bed mixers and continuously operating vertical mixers in which the polymer structure is mixed by means of rotating blades in rapid frequency (Schugi mixer).
• the polymer structure or the polymer gel in the postcrosslinking is preferably at most 20% by weight, particularly preferably at most 15% by weight, moreover preferably at most 10% by weight, moreover still more preferably at most 5% by weight.
• condensation crosslinkers are those which have been mentioned in WO-A-2004/037903 as crosslinkers of crosslinking classes II.
• crosslinking agents are condensation crosslinkers such as, for example, diethylene glycol, triethylene glycol, polyethylene glycol, glycerol, polyglycerol, propylene glycol, diethanolamine, triethanolamine, polyoxypropylene, oxyethylene-oxypropylene block copolymers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, trimethylolpropane, pentaerytritol , Polyvinyl alcohol, sorbitol, 1,3-dioxolan-2-one (ethylene carbonate), 4-methyl-1,3-dioxolan-2-one (propylene carbonate), 4,5-dimethyl-1,3-dioxolan-2-one , 4,4-dimethyl-1,3-dioxolan-2-one, 4-ethyl-1,3-dioxolan-2-one, 4-hydroxymethyl-1,3-dioxolan-2-one
• the duration of the heat treatment is limited by the risk that the desired property profile of the polymer structures is destroyed as a result of the action of heat.
• the surface modification in process step v) may also comprise the treatment with a compound containing aluminum, preferably Al 3+ ions, it being preferred that this treatment is carried out simultaneously with the surface postcrosslinking, by a preferably aqueous solution containing the Post-crosslinked and the compound containing aluminum, preferably Al 3+ ions, brought into contact with the water-absorbing polymer structures and then heated.
• the compound containing aluminum is contained in an amount within a range of 0.01 to 30% by weight, more preferably in an amount within a range of 0.1 to 20% by weight, and further preferably in an amount in a range of 0.3 to 5 wt .-%, each based on the weight of the water-absorbing polymer structures, is brought into contact with the water-absorbing polymer structures.
• Preferred aluminum-containing compounds are water-soluble compounds containing Al 3+ ions, such as A1C1 3 x 6H 2 0, NaAl (S0 4) 2 x 12 H 2 0, KA1 (S0 4) 2 x 12 H 2 0 or Al 2 (S0 4 ) 3 ⁇ 14-18 H 2 O, aluminum lactate or water-insoluble aluminum compounds, such as aluminum oxides, for example Al 2 O 3 , or aluminates. Particular preference is given to using mixtures of aluminum lactate and aluminum sulfate.
• the water-absorbing polymer structures provided in process step I) are modified with a plasma, the water-absorbing polymer structures being mixed together during process step II).
• ⁇ / asma as used herein is understood to mean an at least partially ionized gas which contains a significant proportion of free charge carriers such as ions or electrons, for example, by means of electrical glow discharges by means of direct current.
• the generation of a plasma by means of low-frequency excitation is particularly preferred according to the present invention. More preferably, the excitation frequency is in the range of 1 to 10 11 Hz, more preferably in the range of 1 to 10 10 Hz and most preferably in a range of 1 Hz to 100 kHz.
• the above gases are used in the generation of the plasma with a specific gas flow in a range of 1 to 1000 ml / min, more preferably in a range of 10 to 200 ml / min, and most preferably in a range of 50 to 100 ml / min used.
• the treatment of the surface of the water-absorbing polymer structures provided in process step I) with the plasma in a range of 10 "6 s to 10 6 sec, more preferably in a range of 10 to 360 min, and most preferably in a Range of 30 to 90 minutes, wherein the duration of the treatment with the plasma in particular depends on the amount of water-absorbing polymer structures used and on the power fed into the plasma.
• the plasma is a low-pressure plasma.
• the water-absorbing polymer structures are now mixed with one another during their modification by the above-described plasma, wherein the term "mixing" preferably means any measure which leads to a relative movement of the water-absorbing particles to one another.
• mixing devices known to those skilled in the art can be used as the mixing device, in which a plasma can be generated by suitable modifications within the mixing chamber, so that the surfaces of the water-absorbing polymer structures located in the mixing chamber are always exposed to the plasma during mixing.
• Particularly suitable are drum mixers, Patterson elley mixers, DRAIS turbulence mixers, Lödigemischer, Ruberg mixers, screw mixers, plate mixers, fluidized bed mixers and continuously operating vertical mixer (Schugi mixer), which were modified such that by means of a generator high-frequency alternating electric field between two electrodes is generated in order to put a gas in the mixing chamber by preferably capacitive coupling of an electric field in the plasma state, whereby a phase-shifted plasma comes into consideration.
• the modification of the water-absorbing polymer structures in process step II) takes place in a drum, preferably rotating about a horizontal axis, in which a plasma is generated.
• the electrodes, which serve to generate the plasma are mounted on two opposite sides of the rotating drum parallel to the axis of rotation about which the drum rotates.
• drum is designed in the form of a cylinder of length L and circumference U, it is particularly advantageous according to the invention if the two are themselves
• Each of the two electrodes when disposed opposite each other, together cover at least 75%, more preferably at least 90% and most preferably at least 95% of the circumference of the cylinder and extend over a length of at least 75 %, more preferably at least 90% and most preferably at least 95% of the length L of the cylinder. In this way it can be ensured that as far as possible the entire interior of the rotating drum is filled by the plasma.
• the absorption rate of the water-absorbing polymer structures can be particularly increased by the plasma treatment, especially when the amount of water-absorbing polymer structure used is limited when using a drum rotating about a horizontal axis. It has proven to be particularly advantageous if the water-absorbing polymer structures used in an amount of at most 0.8 g / cm 3 , more preferably at most 0.75 g / cm 3 and most preferably at most 0.5 g / cm 3 drum volume become.
• the water-absorbing polymer structures before or during the process step II) with 0.001 to 5 wt .-%, particularly preferably 0, 1 to 2.5 wt .-% and most preferably 0.25 to 1 wt .-%, each based on the total weight of the water-absorbing polymer structures, a filler are mixed.
• the filler may be in atomic monolayers, with 1 to 10 of these monolayers being preferred.
• fillers in particular come Si-O compounds, preferably zeolites, fumed silicas such as Aerosils ®, into consideration.
• the plurality of water-absorbing polymer structures are mixed with a plurality of inorganic particles.
• Suitable inorganic particles are in principle all those which appear suitable to the person skilled in the art for mixing with water-absorbing polymer structures.
• oxides are preferred, with oxides of IV. Group being particularly preferred, and Si oxides are furthermore preferred.
• the Si oxides are zeolites, fumed silicas such as Aerosils ® or Sipernat ®, preferably Sipernat ® preferred.
• the inorganic particles may be used in any amount that appears to those skilled in the art as useful for improving the properties of the water-absorbing polymer structure.
• the inorganic particles are in an amount in the range of 0.001 to 15 wt .-%, preferably in a range of 0.01 to 10 wt .-% and particularly preferably in a range of 2 to 7 wt .-%, respectively based on the water-absorbing polymer particles used.
• the inorganic particles can be used in all particle sizes which appear suitable for the person skilled in the art in order to improve the properties of the water-absorbing polymer structure.
• a further contribution to the present invention provides a device for producing a plasma-treated water-absorbing polymer structure, comprising fluid-conducting interconnected and directly or indirectly successively as device components:
• the plasma treatment region includes a plasma source and a mixing device, preferably a rotary mixing device.
• the polymerization region preferably includes a ribbon or screw extrusion polymerization device.
• the packaging area preferably includes a drying and crushing device.
• WO 05/122075 A1 further discloses further details of the surface postcrosslinking area, referred to therein as a postcrosslinking area.
• WO 02/122075 AI in connection with other device details.
• fluid-conducting means that liquids, gels, powders or other flowable phases can be moved into the individual regions. This can be done through pipes, pipes or gutters and also by conveyors or pumps.
• the surface-modified water-absorbing polymer structures according to the invention are characterized by an FSR value determined according to the test method described herein of at least 0.3 g / g / sec, more preferably at least 0.32 g / g / sec, more preferably at least 0.34 g / g / sec, more preferably still 0.36 g / g / sec, and most preferably at least 0.38 g / g / sec. In general, 0.8 or 1 g / g / sec are not exceeded.
• the water-absorbing polymer structures according to this particular embodiment are characterized by a retention determined according to the test method described here of at least 26.5 g / g, more preferably at least 27.5 g / g and most preferably at least 28.5 g / g , As a rule, 40 or even 42 g / g are not exceeded.
• a retention determined according to the test method described here of at least 26.5 g / g, more preferably at least 27.5 g / g and most preferably at least 28.5 g / g , As a rule, 40 or even 42 g / g are not exceeded.
• the surface-modified water-absorbing polymer structures according to the invention are characterized by an absorption determined under the test method described herein under pressure of at least 20 g / g, more preferably at least 23 g / g and most preferably at least 24 g / g. As a rule, 30 or even 32 g / g are not exceeded.
• a composite comprising the surface-modified water-absorbing polymer structures according to the invention and a substrate. It is preferred that the surface-modified water-absorbing polymer structures and the substrate are firmly joined together.
• films of polymers such as of polyethylene, polypropylene or polyamide, metals, nonwovens, fluff, tissues, fabrics, natural or synthetic fibers, or other foams are preferred.
• the composite comprises at least one region which comprises the surface-modified water-absorbing polymer structures according to the invention in an amount in the range of about 15 to 100% by weight, preferably about 30 to 100% by weight, more preferably about 50 to 99.99 wt .-%, further preferably from about 60 to 99.99 wt .-% and more preferably from about 70 to 99 wt .-%, each based on the total weight of the respective region of the composite includes This range preferably has a size of at least 0.01 cm 3 , preferably at least 0.1 cm 3 and most preferably at least 0.5 cm 3 .
• the composite according to the invention is a sheet-like composite, as described in WO-A-02/056812 as "absorbent materia '.
• a further contribution to achieving the abovementioned objects is provided by a process for producing a composite, wherein the surface-modified water-absorbing polymer structures according to the invention and a substrate and
• the substrates used are preferably those substrates which have already been mentioned above in connection with the composite according to the invention.
• a contribution to achieving the abovementioned objects is also provided by a composite obtainable by the process described above, this composite preferably having the same properties as the composite according to the invention described above.
• chemical products comprising the surface-modified water-absorbing polymer structures according to the invention or a composite according to the invention.
• Preferred chemical products are, in particular, foams, shaped articles, fibers, films, cables, sealing materials, liquid-absorbent hygiene articles, in particular diapers and sanitary napkins, carriers for plant- or fungi-growth-regulating agents or crop protection active ingredients, additives for building materials, packaging materials or floor additives.
• the use of the surface-modified water-absorbing polymer structures according to the invention or of the composite according to the invention in chemical products, preferably in the abovementioned chemical products, in particular in hygiene articles such as diapers or sanitary napkins, and the use of the superabsorbent particles as carriers for plant- or fungi-growth-regulating agents or crop protection active ingredients contribute to solve the problems mentioned above.
• the plant or fungi growth regulating agents or crop protection actives can be delivered for a period of time controlled by the carrier.
• FIG. 1 shows a first embodiment of a designed as a drum device, which can be used to carry out the method according to the invention.
• FIG. 2 shows a second embodiment of a device designed as a drop tower which can be used to carry out the method according to the invention.
• FIG. 3 shows an embodiment of a polymerization device according to the invention which can be used to carry out the method according to the invention.
• the water-absorbing polymer structures 3 are placed in a drum 1 rotating about a horizontal axis. Outside the drum two opposing electrodes 2 are arranged, by means of which inside the drum 1, a plasma can be generated. Within the drum stirring paddles or other device components which allow a better mixing of the water-absorbing polymer structures may be provided (not shown in FIG. 1). In the embodiment of the method according to the invention shown in FIG. 2, the water-absorbing polymer structures 3 fall downwards in a drop tower 1. On the way down they pass a plasma, which is generated by two opposite electrodes 2 outside the drop tower 1.
• FIG. 3 shows an exemplary embodiment of a device 4 according to the invention. This is followed by a confectioning region 6 on a polymerization region 5, followed by a plasma treatment region 7 followed by a surface crosslinking region. Apart from the fact that further regions can be provided between the regions shown here, the plasma treatment region 7 has a plasma source 8 and a mixing device 10. The plasma treatment area 7 may be executed as shown in FIG. 1 or 2. In addition, further details on the design of the areas except the plasma treatment area from WO 05/722075 AI arise.
• the absorption rate was determined by measuring the so-called "Free Swell Rate - FSR" according to the test method described in EP-A-0 443 627 on page 12. The determination is carried out for the particle fraction in a range of 300 to 600 ⁇ .
• AAP absorption against a pressure of 0.7 psi (about 50 g / cm 2 ) is determined according to ERT 442.2-02, with “ERT” for “EDANA recommended test” and “EDANA” for European disposables and Nonwovens Association. "The determination is made for the particle fraction in a range of 300 to 600 ⁇ .
• CRC retention referred to as "CRC” is determined according to ERT 441.2-02 The determination is carried out for the particle fraction in a range from 300 to 600 ⁇ m
• a drum shown in Fig. 1 as a cross-sectional view rotating about a horizontal axis 15 g of water-absorbing polymer structures are used as starting material.
• a rotating drum a DURAN ® glass bottle from Schott Germany
• externally attached electrodes see Figure 1 with an output of about 90 watts
• Non-surface-postcrosslinked water-absorbing polymer structures (powder A) and surface-postcrosslinked water-absorbing polymer structures (powder B) were used as the starting material.
• powder A 100 g of powder A are carefully mixed homogeneously with 0.5 g of Siperant 22S from Evonik Degussa GmbH in a beaker by means of a spatula and subjected to a plasma treatment as in Example 1 in order to obtain powder C.
• the FSR values are given in Table 2.

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• Chemical & Material Sciences (AREA)
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• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Dispersion Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Toxicology (AREA)
• Physics & Mathematics (AREA)
• Engineering & Computer Science (AREA)
• Plasma & Fusion (AREA)
• Processes Of Treating Macromolecular Substances (AREA)
• Treatments Of Macromolecular Shaped Articles (AREA)
• Absorbent Articles And Supports Therefor (AREA)
• Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
• Solid-Sorbent Or Filter-Aiding Compositions (AREA)

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• 2009
  • 2009-09-11 DE DE102009040949A patent/DE102009040949A1/de not_active Ceased
• 2010
  • 2010-08-18 KR KR1020127009305A patent/KR20120090063A/ko not_active Application Discontinuation
  • 2010-08-18 CN CN2010800397196A patent/CN102482441A/zh active Pending
  • 2010-08-18 US US13/389,745 patent/US20120145956A1/en not_active Abandoned
  • 2010-08-18 WO PCT/EP2010/062028 patent/WO2011029704A1/de active Application Filing
  • 2010-08-18 EP EP10742855A patent/EP2475708A1/de not_active Withdrawn
  • 2010-08-18 JP JP2012528298A patent/JP5642792B2/ja not_active Expired - Fee Related
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