EP0076888B1 - Saugfähiges Flächengebilde und Verfahren zu seiner Herstellung - Google Patents

Saugfähiges Flächengebilde und Verfahren zu seiner Herstellung Download PDF

Info

Publication number
EP0076888B1
EP0076888B1 EP82103019A EP82103019A EP0076888B1 EP 0076888 B1 EP0076888 B1 EP 0076888B1 EP 82103019 A EP82103019 A EP 82103019A EP 82103019 A EP82103019 A EP 82103019A EP 0076888 B1 EP0076888 B1 EP 0076888B1
Authority
EP
European Patent Office
Prior art keywords
weight
fibre
latex
fibres
suspension
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.)
Expired
Application number
EP82103019A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0076888A2 (de
EP0076888A3 (en
Inventor
Michel Dr. Pässler
Bruno Reisch
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.)
Carl Freudenberg KG
Original Assignee
Carl Freudenberg KG
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 Carl Freudenberg KG filed Critical Carl Freudenberg KG
Publication of EP0076888A2 publication Critical patent/EP0076888A2/de
Publication of EP0076888A3 publication Critical patent/EP0076888A3/de
Application granted granted Critical
Publication of EP0076888B1 publication Critical patent/EP0076888B1/de
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4266Natural fibres not provided for in group D04H1/425
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/425Cellulose series
    • D04H1/4258Regenerated cellulose series
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4326Condensation or reaction polymers
    • D04H1/435Polyesters
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/64Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
    • D04H1/68Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions the bonding agent being applied in the form of foam
    • 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
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31826Of natural rubber
    • 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.]
    • Y10T442/30Woven fabric [i.e., woven strand or strip material]
    • Y10T442/3325Including a foamed layer or component
    • Y10T442/3366Woven fabric is coated, impregnated, or autogenously bonded
    • 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]
    • Y10T442/647Including a foamed layer or component
    • Y10T442/652Nonwoven fabric is coated, impregnated, or autogenously bonded

Definitions

  • the invention relates to an absorbent sponge cloth with pores and made of a latex-bonded fiber material, which can contain a reinforcement made of woven, knitted, foam, nonwoven or abrasive nonwoven.
  • An expedient method for producing such sponge cloths is also described.
  • Sponge cloths are used in particular as household towels. They are known in different versions. For example, it is possible to impregnate nonwovens, in particular nonwovens or fabrics consolidated by needles, with a heat-coagulable latex as a binder. The textile fabric is immersed in the aqueous dispersion of the latex and the amount of latex is regulated by pressing with suitable press rollers.
  • a household cloth is the subject of DE-A-2 824 715.
  • the cloth is absorbent in a certain sense, but it has no properties similar to natural sponges, in particular it does not contain any open pores. Because of its lack of usage properties, it is not produced on a large scale and has just as little practical importance as rubber or polyurethane sponge cloths. Sponges and window cloths made of cross-linked polyvinyl alcohol also have poor performance properties because such products are hard and brittle when dry.
  • viscose sponge cloths which mostly contain a fabric to increase the tensile strength. Since the viscose sponge cloth is hard and brittle when dry, an impregnation with dilute softening solution, e.g. B. glycerin, proposed. While the viscose sponge cloth does not withstand any mechanical stress in the absolutely dry state without this plasticizer additive and absorbs around 10% moisture when air-conditioned, the moisture absorption in a "softened” cloth is around 20%. In practical use, where the cloth dries only by leaving it lying around, a cloth that is subjectively perceived as dry still contains at least 15 to 20% moisture, which is sufficient to not let the cloth become completely brittle.
  • dilute softening solution e.g. B. glycerin
  • a viscose sponge cloth which contains polyolefin fibers of different lengths and in different proportions to improve the wiping effect on greasy and water-repellent surfaces and to avoid the appearance of streaks, wiping pores and cleaning strips.
  • the fiber content is up to 80% by weight.
  • the cloth is manufactured using the traditional xanthate process.
  • the improvement of this viscose sponge cloth compared to the cloths described above essentially consists in the better cleaning properties.
  • the hard grip and the brittleness in the dry state are not reduced by mixing in the fibers.
  • the environmental impact of the xanthate process has not been eliminated.
  • the invention is based on the object of developing such a sponge cloth that does not have the known disadvantages of the viscose sponge cloth with high water absorption and good suction speed.
  • the cloth should be soft and pleasant to the touch, especially when dry, and should not show any bacteria or fungi.
  • plasticizers, pore formers or similar substances that interfere with use and change the properties of the cloth during use should be avoided.
  • Another object of the invention is the development of an environmentally friendly method for producing the novel sponge cloths.
  • the object according to the invention is achieved by the sponge cloth described in the claims and by the method for its production, which is also specified.
  • the sponge cloth according to the invention contains a hydrophilic fiber material which is latex-bonded and has essentially open pores.
  • a hydrophilic fiber material which is latex-bonded and has essentially open pores.
  • the nonwoven fabric can also contain mineral abrasives, so that the nonwoven fabric side has an abrasive effect.
  • the fiber material consists of a mixture of hydrophilic staple fibers of different lengths and optionally fiber dust, pulp, wood pulp, linters or the like.
  • hydrophobic staple fibers made of synthetic material can be added as an admixture.
  • the fiber mixture is embedded in an open-pore foam, which expediently consists of heat-coagulable latex. Without any addition of salts or other pore formers, the latex is foamed using a gaseous medium, preferably with air.
  • the fiber / latex ratio is expediently in the range from 80:20 to 10:90% by weight.
  • the fiber material from the mixture described above is mixed with the latex mixture in an aqueous suspension according to a preferred method and then foamed with air.
  • the resulting foam mass is applied to a textile carrier and fixed by coagulation by the action of heat.
  • the fiber-latex structure is then dried together with the carrier material in order to obtain a coherent structure.
  • the sponge cloth according to the invention differs decisively both from the raw materials and with regard to the production process from the known viscose sponge cloths. While the viscose sponge cloth over the cellulose xanthate with salts, e.g. B. sodium sulfate, is produced as a pore former, the cloth according to the invention can be produced without pore former.
  • the mass, which is only foamed with air, is fixed in its shape. The fixed latex foam is vulcanized during or after drying
  • the fiber mixture is processed into the fiber foam in a 5 to 30% by weight suspension, based on its total weight.
  • a wetting agent can be added. It is usually advisable to use a 10% by weight suspension.
  • the latex mixture can either be added to this foam without being foamed or it can also be already foamed. It is advisable to use heat-sensitive latex mixtures that are coagulated by heat after application to the reinforcing fabric, knitted fabric, foam or nonwoven fabric. The fabric fixed in this way is dried and then vulcanized.
  • the sponge cloth according to the invention has a soft feel even in the dry state and, unlike viscose sponge cloths, can therefore be commercially available dry packaged without the addition of water and plasticizers. It is therefore hygienically harmless, while the moist packaged viscose sponge cloths can always be infected by bacteria or fungi.
  • the sponge cloth is essentially open-pored.
  • the cell walls are severely broken.
  • the product is very similar to the natural sponge with its dense tangle of fibrils and extensive cavities.
  • the material according to the invention can have hydrophilic properties both with respect to the fibers and with respect to the latex. In the dry state it is soft and elastic, while the elasticity is essentially retained even when wet. When wetting takes place very quickly, the material absorbs several times its own weight in water.
  • the fiber-latex ratio is between 80: 20 and 10: 90% by weight.
  • Cellulose short cuts with a fiber length of about 2 to 16 mm are proposed as hydrophilic, absorbent fibers, furthermore cellulose, cellulose dust, cotton dust, linters, wood pulp, polyvinyl alcohol fibers and mixtures of the above-mentioned components.
  • fiber components of up to 100% by weight of cotton dust, up to 50% by weight of cellulose and 10 to 50% by weight of short cotton cuts (1.7 to 22 dtex) are recommended.
  • fibers with a length of 5 to 8 mm are preferred.
  • Polyamide, polyester, polypropylene or polyacrylonitrile fibers are suitable as hydrophobic synthetic short cut fibers.
  • the synthetic fibers are expediently added in an amount of 2 to 30% by weight.
  • the weight fractions relate to the total weight of the fiber mixture. For better processability, 0.5 to 2% by weight of conventional wetting agents are expediently added.
  • the latex mixture consists of conventional acrylates, methacrylates, polyurethanes, butadiene-acrylonitrile copolymers or butadiene-styrene copolymers, it being advisable to use heat-coagulable mixtures, the composition of which can be determined by simple preliminary tests.
  • a 10% by weight fiber suspension is foamed to a liter weight of 200 to 500 g.
  • the non-foamed or foamed latex mixture is added to this foam, the mixture of both components being expediently used to a liter weight of 200 to 500 g.
  • the coagulation point of the heat-sensitive mixture is expediently between 30 ° and 60 ° C.
  • the foamed mixture is applied to a reinforcing carrier made of woven, knitted, foam or nonwoven and coagulated under the action of heat.
  • a pattern can be embossed for optical reasons.
  • After drying at about 130 ° C is then vulcanized, for. B. at 150 ° C.
  • the cloth is then washed out. Most of the water is removed by squeezing or suction and the pre-dewatered structure is dried again by the action of heat.
  • the backing material coated on one or both sides remains as a reinforcement in the finished sponge cloth.
  • the hydrophilic properties of the cloth can be varied according to the intended use.
  • a further variation is also possible through a suitable choice of latex.
  • rubber latex made from butadiene acrylonitrile, butadiene styrene and their diverse copolymers, if appropriate together with other copolymers, is also suitable as latex.
  • aqueous dispersions of polyurethanes are also suitable.
  • 106 g of butadiene acrylonitrile latex with a solids content of 47% by weight is adjusted to heat sensitivity using conventional additives (sulfur, zinc oxide, vulcanization accelerators, organopolysiloxanes, etc.) (coagulation point 55 to 60 ° C.) and foamed to twice the volume.
  • 350 g of a 10% by weight cellulose dust / cotton dust suspension (cellulose / cotton 1: 1) are introduced into the foam and the entire mass is foamed to a final volume of 1100 ml.
  • the foam mass is applied to a textile carrier material (cellulose fleece, 50 g / m 2 ), coagulated and dried at 130 ° C.
  • the material thus produced is soft and has closely spaced pores of approximately 0.5 to 1 mm in diameter. The material absorbs four times its own weight in water.
  • 106 g of butadiene acrylonitrile latex with a solids content of 47% by weight is adjusted to heat sensitivity using conventional additives (as in Example 1) (coagulation point 55 to 60 ° C.) and foamed to twice the volume.
  • 200 g of a 10% by weight pulp suspension containing a wetting agent are stirred in, producing 650 ml of foam.
  • the mass is applied to a 50 g / m 2 cellulose fleece, coagulated, dried at 130 ° C and vulcanized at 150 ° C. After washing, it is dried again.
  • the result is a heavy material with very good strength.
  • the rather layer-like structure has pores of very different sizes of approximately 0.5 to 4 mm in diameter. With this material, a sink can be weighted to dryness.
  • the latex foam produced as in Example 2 is mixed with 400 g of foam, which is produced by foaming a 10% by weight suspension of 75% by weight cellulose and 25% by weight fiber dust from 50% by weight cellulose and 50% % By weight of cotton dust, water and wetting agent was obtained. 1700 ml of foam are produced.
  • the foam mass is applied approximately 2.5 mm thick to an approximately 50 g / m 2 nonwoven fabric made of cellulose fibers, coagulated at 55 ° C and pre-dried at 130 ° C.
  • the back of the nonwoven fabric is treated in the same way and the product is then vulcanized at 150 ° C. and then washed out and dried again.
  • the pores of the material are separated by very thin layers of material, so that there is a loose structure and a soft feel.
  • 142 g of a latex foam made of polybutadiene acrylonitrile with a solids content of 42% by weight and a liter weight of 475 g are mixed with 350 g of a foam which is made by foaming a 10% by weight cellulose dust and cotton dust suspension (50% cellulose dust and 50 wt .-% cotton dust) was obtained.
  • the foam mass is applied to a carrier made of 2 mm thick foam, coagulated at 50 ° C and stamped with a pattern. After predrying, the back is also coated, coagulated at 50 ° C and also provided with a sample. After drying and vulcanization at 140 or 160 ° C, the material is washed out and mechanically freed of water by squeezing.
  • the very soft, spring-elastic cloth has a very low basis weight (289 g / m 2 ).
  • 180 g of latex mixture made of polybutadiene acrylonitrile with a solids content of 35.5% by weight and containing 10 g of chalk are foamed to 350 ml.
  • 17.5 g of cotton dust, 8.8 g of bleached cellulose and 15.1 g of cellulose short cut fibers 5.6 / 6 (58%) are made up to 1200 with 330 g of water and 25 g of oleoyl methyl tauride as a wetting agent (24%) ml foam volume brought. Both foams are combined and foamed to a total of 2100 ml.
  • the mass is applied 2.5 mm thick to a cellulose fabric (mesh size 1 x 3 mm) and coagulated at 47 ° C. After the pattern is pre-dried and the back of the cellulose fabric coated, coagulated and embossed in the same way. After drying at 130 ° C is vulcanized at 150 °, then washed out and dried again.
  • the sponge cloth obtained according to this example has particularly favorable combinations of properties.
  • the material is very soft and pleasant to the touch, has good strength and a low basis weight with a very open pore structure. It can be cooked without losing its structure and strength.
  • Example 5 180 g of latex mixture as in Example 5 are added without foaming to 399 g of fiber suspension which has been foamed to 1000 ml.
  • the fiber blend contains 25% cotton dust, 25% cellulose dust, 25% cellulose, 10% cellulose short cut fibers 5,6 / 8 and 15% polyester short cut fibers 3,3 / 8.
  • the mixture of latex compound and fiber scarf is foamed to 2,150 ml.
  • the mass is applied as in Example 5, dried and vulcanized.
  • the material has a slightly harder grip than the material obtained in Example 5 and is characterized by a high tear strength with a very low basis weight.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Nonwoven Fabrics (AREA)
  • Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Paper (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
EP82103019A 1981-10-14 1982-04-08 Saugfähiges Flächengebilde und Verfahren zu seiner Herstellung Expired EP0076888B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3140784 1981-10-14
DE19813140784 DE3140784A1 (de) 1981-10-14 1981-10-14 "saugfaehiges flaechengebilde und verfahren zu seiner herstellung"

Publications (3)

Publication Number Publication Date
EP0076888A2 EP0076888A2 (de) 1983-04-20
EP0076888A3 EP0076888A3 (en) 1985-09-11
EP0076888B1 true EP0076888B1 (de) 1988-11-23

Family

ID=6144076

Family Applications (1)

Application Number Title Priority Date Filing Date
EP82103019A Expired EP0076888B1 (de) 1981-10-14 1982-04-08 Saugfähiges Flächengebilde und Verfahren zu seiner Herstellung

Country Status (10)

Country Link
US (1) US4559243A (es)
EP (1) EP0076888B1 (es)
JP (2) JPS5876434A (es)
AU (1) AU553566B2 (es)
DD (1) DD202107A5 (es)
DE (2) DE3140784A1 (es)
ES (1) ES516474A0 (es)
FI (1) FI77973C (es)
NO (1) NO162492C (es)
YU (1) YU42597B (es)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3447499A1 (de) * 1984-12-27 1986-07-10 PWA Waldhof GmbH, 6800 Mannheim Nicht-trocknendes reinigungstuch
JPS6333434A (ja) * 1986-07-28 1988-02-13 Nippon Rubber Co Ltd フオ−ムラバ−の製造法
JPH02109562A (ja) * 1988-10-19 1990-04-23 Lion Corp 吸収性物品
JPH02175355A (ja) * 1988-12-27 1990-07-06 Sumiko Nagamori つや出しシート
GB9011378D0 (en) * 1990-05-22 1990-07-11 Bio Isolates Ltd Cellulosic sponge adsorbent medium
US5049439A (en) * 1990-05-25 1991-09-17 Fibre Converters, Inc. Thermoformable article
DE4205547C1 (es) * 1992-02-24 1993-01-21 Fa. Carl Freudenberg, 6940 Weinheim, De
JPH0591548U (ja) * 1992-05-12 1993-12-14 千代田株式会社 ワイパー
US5690996A (en) * 1992-11-02 1997-11-25 Sepragen Cross-linked cellulose sponge
DE4422373A1 (de) * 1994-06-27 1996-01-04 Henkel Ecolab Gmbh & Co Ohg Wischbezug für ein Fußbodenwischgerät
US5908319A (en) * 1996-04-24 1999-06-01 Ulvac Technologies, Inc. Cleaning and stripping of photoresist from surfaces of semiconductor wafers
US5968853A (en) * 1997-03-10 1999-10-19 The Procter & Gamble Company Tissue with a moisture barrier
US5965030A (en) * 1997-04-15 1999-10-12 Rohm And Haas Company Reusable mat for removing liquid contaminants
FR2767541B1 (fr) * 1997-08-21 1999-10-08 Hutchinson Matiere spongieuse, son procede de fabrication et ses applications
US6261679B1 (en) 1998-05-22 2001-07-17 Kimberly-Clark Worldwide, Inc. Fibrous absorbent material and methods of making the same
US6479415B1 (en) * 1998-06-08 2002-11-12 Bki Holding Corporation Absorbent structures having fluid acquisition and distribution layer
US6403857B1 (en) 1998-06-08 2002-06-11 Buckeye Technologies Inc. Absorbent structures with integral layer of superabsorbent polymer particles
ATE317270T1 (de) 2000-04-26 2006-02-15 Dow Global Technologies Inc Dauerhafter saugfähiger latexschaumstoff mit verbesserten vertikalen dochteigenschaften
US6607783B1 (en) 2000-08-24 2003-08-19 Kimberly-Clark Worldwide, Inc. Method of applying a foam composition onto a tissue and tissue products formed therefrom
US6503412B1 (en) 2000-08-24 2003-01-07 Kimberly-Clark Worldwide, Inc. Softening composition
KR100816630B1 (ko) 2000-11-08 2008-03-24 킴벌리-클라크 월드와이드, 인크. 티슈 제품의 폼 처리
GB0128438D0 (en) * 2001-11-28 2002-01-16 Mbt Holding Ag Method
US6706944B2 (en) 2001-12-14 2004-03-16 Kimberly-Clark Worldwide, Inc. Absorbent materials having improved absorbent properties
US6939914B2 (en) 2002-11-08 2005-09-06 Kimberly-Clark Worldwide, Inc. High stiffness absorbent polymers having improved absorbency rates and method for making the same
US20030139715A1 (en) * 2001-12-14 2003-07-24 Richard Norris Dodge Absorbent materials having high stiffness and fast absorbency rates
US6689934B2 (en) 2001-12-14 2004-02-10 Kimberly-Clark Worldwide, Inc. Absorbent materials having improved fluid intake and lock-up properties
US6805965B2 (en) 2001-12-21 2004-10-19 Kimberly-Clark Worldwide, Inc. Method for the application of hydrophobic chemicals to tissue webs
US6835418B2 (en) 2002-05-31 2004-12-28 Kimberly-Clark Worldwide, Inc. Use of gaseous streams to aid in application of foam to tissue products
US6797319B2 (en) 2002-05-31 2004-09-28 Kimberly-Clark Worldwide, Inc. Application of foam to tissue products using a liquid permeable partition
US6797116B2 (en) 2002-05-31 2004-09-28 Kimberly-Clark Worldwide, Inc. Method of applying a foam composition to a tissue product
DE10247241A1 (de) * 2002-10-10 2004-04-22 Basf Ag Superabsorbierender Schaum, Verfahren zu seiner Herstellung und seine Verwendung
US6977026B2 (en) 2002-10-16 2005-12-20 Kimberly-Clark Worldwide, Inc. Method for applying softening compositions to a tissue product
US6761800B2 (en) 2002-10-28 2004-07-13 Kimberly-Clark Worldwide, Inc. Process for applying a liquid additive to both sides of a tissue web
US6964725B2 (en) 2002-11-06 2005-11-15 Kimberly-Clark Worldwide, Inc. Soft tissue products containing selectively treated fibers
US7029756B2 (en) 2002-11-06 2006-04-18 Kimberly-Clark Worldwide, Inc. Soft tissue hydrophilic tissue products containing polysiloxane and having unique absorbent properties
US6949168B2 (en) 2002-11-27 2005-09-27 Kimberly-Clark Worldwide, Inc. Soft paper product including beneficial agents
US20040115419A1 (en) * 2002-12-17 2004-06-17 Jian Qin Hot air dried absorbent fibrous foams
US20040121680A1 (en) * 2002-12-23 2004-06-24 Kimberly-Clark Worldwide, Inc. Compositions and methods for treating lofty nonwoven substrates
US7396593B2 (en) 2003-05-19 2008-07-08 Kimberly-Clark Worldwide, Inc. Single ply tissue products surface treated with a softening agent
DE602004015281D1 (de) * 2003-05-30 2008-09-04 Constr Res & Tech Gmbh Zusatzmittel für spritzzementzusammensetzungen
JP4452473B2 (ja) * 2003-09-19 2010-04-21 Basfポゾリス株式会社 液状急結剤
ES2245228B1 (es) * 2004-04-12 2007-07-16 Jose Ramon Ferrandez Llopis Procedimiento de vulcanizacion de laminas de latex y lamina asi obtenida.
GB0416791D0 (en) * 2004-07-28 2004-09-01 Constr Res & Tech Gmbh Setting accelerator for sprayed concrete
US7799169B2 (en) 2004-09-01 2010-09-21 Georgia-Pacific Consumer Products Lp Multi-ply paper product with moisture strike through resistance and method of making the same
FR2905376B1 (fr) * 2006-08-29 2012-10-05 Hutchinson Nouveau materiau absorbant et son procede de preparation.
FR2928383B1 (fr) 2008-03-06 2010-12-31 Georgia Pacific France Feuille gaufree comportant un pli en materiau hydrosoluble et procede de realisation d'une telle feuille.
US20140134217A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Leave-on compositions containing cellulose materials
US20140134218A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Rinse-off skin care compositions containing cellulosic materials
US9370478B2 (en) 2012-11-09 2016-06-21 Johnson & Johnson Consumer Inc. Skin care compositions containing cotton and citrus-derived materials
DE102014014387B4 (de) * 2014-10-02 2016-05-25 Carl Freudenberg Kg Bi-elastische Einlage
DE102015005089A1 (de) * 2015-04-22 2016-10-27 Carl Freudenberg Kg Thermisch fixierbares Flächengebilde
WO2017079169A1 (en) 2015-11-03 2017-05-11 Kimberly-Clark Worldwide, Inc. Paper tissue with high bulk and low lint
WO2020248026A1 (pt) * 2019-06-12 2020-12-17 Damasceno Maria Zelia Machado Processo de produção de composto biodegradável de borracha natural com fibras vegetais residuais e produto obtido
CN110373956A (zh) * 2019-07-26 2019-10-25 李奎波 一种用于扫地机器人的环保纸浆集尘盒制作方法

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE7409174U (de) * 1974-07-11 Delu Fabrik Becker H & Co Reinigungstuch mit Doppelfunktion
DE7418583U (de) * 1974-09-19 Freudenberg C Reinigungstuch
US2832997A (en) * 1953-09-24 1958-05-06 Goodyear Tire & Rubber Porous sheet material
US3311115A (en) * 1963-10-29 1967-03-28 Buckeye Cellulose Corp Low density aerosol filter
DE1560872A1 (de) * 1964-06-16 1970-06-11 Kalle Ag Verfahren zur Herstellung von Wirrfaservliesen
US3281258A (en) * 1965-02-03 1966-10-25 Textile Rubber & Chem Co Process for gelling frothed rubber latices on fabrics
GB1195233A (en) * 1966-07-26 1970-06-17 Johnson & Johnson Nonwoven fibrous product and method of making the same.
US3508953A (en) * 1967-12-22 1970-04-28 Minnesota Mining & Mfg Hydrophilic polyurethane sponge
FR2044026A5 (en) * 1969-05-06 1971-02-19 Wtz Textile Non-woven textile products
FR2043900A5 (es) * 1969-05-08 1971-02-19 Chomarat & Cie
US3657035A (en) * 1969-07-23 1972-04-18 Nylonge Corp Water absorbent web and its production
DE1941838A1 (de) * 1969-08-16 1971-02-25 Collo Rheincollodium Koeln Gmb Verfahren zum Herstellen von Verbundstoffen,insbesondere solchen fuer die Oberflaechenbearbeitung
DE2164902B2 (de) * 1971-12-28 1976-04-15 Fa. Carl Freudenberg, 6940 Weinheim Verfahren zur herstellung bindemittelgebundener vliesstoffe
DE2656968C3 (de) * 1976-12-16 1980-01-31 Hoechst Ag, 6000 Frankfurt Insbesondere zur Naßreinigung geeigneter, faserartige Teilchen enthaltender, poriger Formkörper aus regenerierter Cellulose
DE2711698C3 (de) * 1977-03-17 1980-03-27 Hoechst Ag, 6000 Frankfurt Zum Scheuern und zur Naßreinigung geeignete Vorrichtung
GB1599236A (en) * 1977-06-06 1981-09-30 Montedison Spa Process for preparing an absorbent mop
JPS5513751A (en) * 1978-07-17 1980-01-30 Yukigaya Kagaku Kogyo Kk Production of foam rubber
DE8004287U1 (de) * 1980-02-18 1980-05-22 Fa. Carl Freudenberg, 6940 Weinheim Reinigungstuch

Also Published As

Publication number Publication date
JPS5876434A (ja) 1983-05-09
ES8400860A1 (es) 1983-12-01
DE3140784C2 (es) 1987-06-11
NO162492C (no) 1990-01-10
NO162492B (no) 1989-10-02
EP0076888A2 (de) 1983-04-20
FI821599A0 (fi) 1982-05-06
ES516474A0 (es) 1983-12-01
AU553566B2 (en) 1986-07-24
FI821599L (fi) 1983-04-15
YU110682A (en) 1984-12-31
AU8465882A (en) 1983-04-21
DD202107A5 (de) 1983-08-31
JPH0332507Y2 (es) 1991-07-10
EP0076888A3 (en) 1985-09-11
US4559243A (en) 1985-12-17
DE3140784A1 (de) 1983-04-28
YU42597B (en) 1988-10-31
JPS63177934U (es) 1988-11-17
NO821896L (no) 1983-04-15
FI77973B (fi) 1989-02-28
FI77973C (fi) 1989-06-12
DE3279227D1 (en) 1988-12-29

Similar Documents

Publication Publication Date Title
EP0076888B1 (de) Saugfähiges Flächengebilde und Verfahren zu seiner Herstellung
DE2721511C2 (de) Adsorbierender, nichtgewebter Stoff und Verfahren zu dessen Herstellung
EP0238476B1 (de) Nubuk-bzw. velourlederartiges Substrat sowie Verfahren zur Herstellung desselben
EP0095527B1 (de) Polsterkörper
DE2737130A1 (de) Verbesserte stapelfaser, ausruestung dafuer sowie verfahren zu deren herstellung
EP3004452B1 (de) Reinigungstuch
DE1901209A1 (de) Verfahren zum Herstellen eines aus Fasern und elastischen Materialien bestehenden Verbundmaterials in Bahnenform
DE1010945B (de) Verfahren zur Herstellung von Kunstleder
WO2014191071A1 (de) Reinigungstuch
DE2244901A1 (de) Dreidimensional verstaerktes schaumpolymer
DE1940772B2 (de) Verfahren zur Herstellung eines flächenhaften, flexiblen, atmungsaktiven Mehrschichtstoffes mit einer florartigen Außenseite
DE3628302C2 (es)
DE2827804A1 (de) Verwendung von modifizierten cellulosehydratfasern fuer gebundene faservliese
DE2253926C3 (de) Verfahren zur Herstellung von kunstlederartigen dünnwandigen Gebilden auf PVC-Basis
EP3592805B1 (de) Reinigungsartikel
DE1419399A1 (de) Verfahren und Dispersion zum Binden von Wirrfaservliesen
US2914493A (en) Cellulose sponge composition containing polyethylene terephthalate fiber and method of making
DE1294342B (es)
AT257177B (de) Poröse, saugfähige Folie und Verfahren zu deren Herstellung
DE1947142A1 (de) Textiles Flaechengebilde und Verfahren zu dessen Herstellung
DE7328452U (de) Reinigungstuch mit Doppelfunktion
DE2364130C3 (de) Kunstleder und Verfahren zu dessen Herstellung
DE2945244A1 (de) Verfahren zur herstellung eines fensterlederartigen,saugfaehigen reinigungstuches
DE102020127588A1 (de) Absorptive Schallisolierungen
KR20010105991A (ko) 항균방취성능이 우수한 인공피혁 제조용 시트의 제조방법

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): BE CH DE FR GB IT LI LU NL SE

17P Request for examination filed

Effective date: 19831006

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): BE CH DE FR GB IT LI LU NL SE

17Q First examination report despatched

Effective date: 19860731

ITF It: translation for a ep patent filed

Owner name: BARZANO' E ZANARDO ROMA S.P.A.

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE CH DE FR GB IT LI LU NL SE

GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)
REF Corresponds to:

Ref document number: 3279227

Country of ref document: DE

Date of ref document: 19881229

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
ITTA It: last paid annual fee
EPTA Lu: last paid annual fee
EAL Se: european patent in force in sweden

Ref document number: 82103019.4

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20010323

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20010404

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20010413

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20010420

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20010423

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20010424

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LU

Payment date: 20010426

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20010504

Year of fee payment: 20

BE20 Be: patent expired

Free format text: 20020408 FIRMA *CARL FREUDENBERG

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20020407

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20020407

Ref country code: CH

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20020407

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20020408

Ref country code: LU

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20020408

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Effective date: 20020407

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

NLV7 Nl: ceased due to reaching the maximum lifetime of a patent

Effective date: 20020408

EUG Se: european patent has lapsed

Ref document number: 82103019.4

NLV7 Nl: ceased due to reaching the maximum lifetime of a patent

Effective date: 20020408