EP1611272A1 - Cellulosed molded article having a functional effect and method for producing the same - Google Patents
Cellulosed molded article having a functional effect and method for producing the sameInfo
- Publication number
- EP1611272A1 EP1611272A1 EP04725036A EP04725036A EP1611272A1 EP 1611272 A1 EP1611272 A1 EP 1611272A1 EP 04725036 A EP04725036 A EP 04725036A EP 04725036 A EP04725036 A EP 04725036A EP 1611272 A1 EP1611272 A1 EP 1611272A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fibers
- cellulosic
- metal ions
- silver
- fiber
- 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.)
- Granted
Links
- 230000000694 effects Effects 0.000 title claims abstract description 11
- 238000004519 manufacturing process Methods 0.000 title abstract description 7
- 239000000835 fiber Substances 0.000 claims abstract description 110
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 25
- 150000002500 ions Chemical class 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 19
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 9
- 239000007864 aqueous solution Substances 0.000 claims abstract description 6
- 229910052709 silver Inorganic materials 0.000 claims description 54
- 239000004332 silver Substances 0.000 claims description 54
- -1 silver ions Chemical class 0.000 claims description 27
- 239000004480 active ingredient Substances 0.000 claims description 14
- 238000000465 moulding Methods 0.000 claims description 14
- 239000004753 textile Substances 0.000 claims description 11
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 10
- 239000004952 Polyamide Substances 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 239000005711 Benzoic acid Substances 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 4
- 235000010233 benzoic acid Nutrition 0.000 claims description 4
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 claims description 4
- 239000004744 fabric Substances 0.000 claims description 4
- 235000010199 sorbic acid Nutrition 0.000 claims description 4
- 239000004334 sorbic acid Substances 0.000 claims description 4
- 229940075582 sorbic acid Drugs 0.000 claims description 4
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 2
- 229910052753 mercury Inorganic materials 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 239000008177 pharmaceutical agent Substances 0.000 claims 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 1
- 235000013580 sausages Nutrition 0.000 claims 1
- 210000002268 wool Anatomy 0.000 claims 1
- 239000013543 active substance Substances 0.000 abstract description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 32
- 150000001768 cations Chemical class 0.000 description 23
- 229920002678 cellulose Polymers 0.000 description 10
- 239000001913 cellulose Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 8
- 230000000845 anti-microbial effect Effects 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 229910001385 heavy metal Inorganic materials 0.000 description 7
- 238000009940 knitting Methods 0.000 description 5
- 239000004971 Cross linker Substances 0.000 description 4
- 241000195493 Cryptophyta Species 0.000 description 4
- 244000299507 Gossypium hirsutum Species 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 229920000058 polyacrylate Polymers 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 244000063299 Bacillus subtilis Species 0.000 description 3
- 235000014469 Bacillus subtilis Nutrition 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000003456 ion exchange resin Substances 0.000 description 3
- 229920003303 ion-exchange polymer Polymers 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- WAZPLXZGZWWXDQ-UHFFFAOYSA-N 4-methyl-4-oxidomorpholin-4-ium;hydrate Chemical compound O.C[N+]1([O-])CCOCC1 WAZPLXZGZWWXDQ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 241000199919 Phaeophyceae Species 0.000 description 2
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 239000013068 control sample Substances 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000002241 glass-ceramic Substances 0.000 description 2
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229960002715 nicotine Drugs 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 125000005208 trialkylammonium group Chemical group 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- VXHYVVAUHMGCEX-UHFFFAOYSA-N 2-(2-hydroxyphenoxy)phenol Chemical compound OC1=CC=CC=C1OC1=CC=CC=C1O VXHYVVAUHMGCEX-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000427940 Fusarium solani Species 0.000 description 1
- 240000001929 Lactobacillus brevis Species 0.000 description 1
- 241001584954 Lactobacillus brevis ATCC 14869 = DSM 20054 Species 0.000 description 1
- 235000003207 Lactobacillus brevis DSM 20054 Nutrition 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000009456 active packaging Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000008275 binding mechanism Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000005341 cation exchange Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000009189 diving Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000009422 growth inhibiting effect Effects 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D01F1/103—Agents inhibiting growth of microorganisms
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
- D06M11/42—Oxides or hydroxides of copper, silver or gold
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/44—Oxides or hydroxides of elements of Groups 2 or 12 of the Periodic Table; Zincates; Cadmates
-
- 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/188—Monocarboxylic acids; Anhydrides, halides or salts thereof
-
- 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
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
- D21H11/20—Chemically or biochemically modified fibres
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/36—Biocidal agents, e.g. fungicidal, bactericidal, insecticidal agents
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
- Y10T428/2905—Plural and with bonded intersections only
Definitions
- the invention relates to a cellulosic molding and to a process for producing cellulosic moldings by the dry-wet extrusion process with improved and extended functional effects, in particular for use in medicine, hygiene, clothing, papermaking and the packaging industry.
- the functional effect relates to a uniform and finely dosed bactericidal action, especially in wound dressings, sports and leisure clothing, hospital textiles, filter and packaging papers.
- heavy metal ions such as silver, mercury, copper, zinc and zirconium ions have a killing or growth-inhibiting effect on microorganisms such as bacteria, viruses, fungi and spores (Thurman et al., CRC Crit Rev. In Environ. Contr. 18 (4) , Pp. 295-315 (1989)).
- microorganisms such as bacteria, viruses, fungi and spores
- the silver ions are of particular interest.
- the decisive advantage of silver ions over other bactericidal metal ions, such. B. Hg 2+ is the most insensitive human metabolism to silver.
- the bactericidal concentration is given as 0.01- 1 mg / L in silver (Ullman's Encyclopedia of Industrial Chemistry (5th ed.), VCH 1993, Volume A 24, p. 160).
- the moldings are capable of adsorbing metals from heavy metal-containing media.
- the heavy metal loaded moldings can be used as antibacterial and / or fungicidal material.
- the content of adsorbed heavy metals in these cellulosic moldings is at least about 70 mg / kg, based on the total weight of the cellulosic molding.
- the invention has for its object to provide a cellulosic molded body and a method for the production of cellulosic moldings having a functional effect, especially for use in medicine, hygiene and clothing, which shows a bactericidal effect and this particular connects with the advantages of a breathable garment.
- Another object is to provide the active ingredients in a textile depot and to ensure a sufficient release of these substances from the depot over time.
- the drug concentration to be delivered should be controllable.
- the shaped bodies produced by the process according to the invention in particular fibers and films, are to be created in such a way that they are suitable for production as wound dressings, patches, hygiene articles, textiles, specialty papers and as packaging material due to their high adsorption capacity. Finally, composites of mixtures with other fibers should be produced.
- Weakly crosslinked ion exchangers for the purposes of the present invention are ion exchangers which are provided with a reduced proportion of crosslinking agents.
- Conventional ion exchange resins have a crosslinker content of 4 to 12% by weight, based on the mass of the exchange resin.
- Weakly crosslinked ion exchangers for the purposes of the present invention have a crosslinker content of 0.1 to 2.0% by weight, preferably 0.3 to 1.5% by weight, more preferably 0.5 to 1.2% by weight.
- Weakly crosslinked ion exchange resins are also characterized by the fact that they swell very strongly in aqueous solutions. Conventional ion exchange resins with the abovementioned crosslinker components have only low degrees of swelling.
- the fibers produced with incorporated weakly crosslinked cation exchangers exceed with their binding capacity for silver ions that of the brown algae according to DE 10 140 772 by up to 28 times. It is thus given the opportunity to produce fibers or films, the z. B. can be highly loaded with cationic bactericidal agents such as silver ions.
- a fiber with 15% by mass of incorporated weakly crosslinked cation exchanger can be loaded with about 80 g of silver. Silver loading of the fiber with> 100 g Ag / kg fiber is possible with a corresponding increase in the mass fraction of the incorporated weakly crosslinked cation exchanger.
- These fibers can then be prepared by mixing with other fibers, such as.
- fibers which have a sufficient content in terms of the silver content per fiber to a sufficient level show bactericidal effect, but show no disadvantages in terms of textile-physical parameters.
- Such fibers show a completely sufficient bactericidal action in the hitherto known fields of use and are equal in their textile-physical values to unmodified fibers. The processing of these fibers and yarns made from them is possible on all textile machines.
- a measure of the expected bactericidal effect of the fibers or yarns is the equilibrium concentration of the active ingredients in aqueous solutions such.
- the free Ag ions are stably discharged, whereby the equilibrium concentration is maintained over time by the Ag deposited in the fiber. Due to the increased depot effect of the fibers according to the invention thus the equilibrium concentration can be maintained over an increased period.
- the fibers can be loaded with cation-active and anionically active bactericidal ions, such as, for example, B. with silver ions and benzoic acid or sorbic acid.
- the loading of the functionalized fibers may conveniently be done by dipping in a solution with the appropriate ions. Diving can be done both in batch mode and continuously. In continuous dipping, preferably the cut fiber is loaded in a separate bath in the after-treatment.
- a 12% by mass cellulose solution in N-methylmorpholine N-oxide monohydrate is a powdered weakly crosslinked cation exchanger based on a crosslinked copolymer of acrylic acid and sodium with a particle size ⁇ 10 microns in a weight fraction of 15% by mass to a cellulose content added.
- This spinning solution is homogenized in a kneader and spun at a temperature of about 90 ° C through a spinneret with 480 holes and a nozzle hole diameter of 80 microns.
- the take-off speed is 30 m / min.
- the multifilament yarn is passed through several washing baths to leach the N-methylmorpholine-N-oxide.
- the fibers are spun off and loaded with 10 liters of a 0.1 M silver nitrate solution per kg of fiber material. After loading, the fibers are spun and washed free from adhering silver nitrate. Subsequently, the fibers are dried at about 80 ° C.
- Table 2 shows the fiber parameters and the silver content of the fiber.
- Such a highly loaded fiber has the advantage that by blending the fiber with other textile fibers such.
- Yarns produced in this way can be processed very well on knitting and knitting machines, in contrast to galvanized polyamide threads.
- Example 2 Fibers are spun according to Example 1 with a titer of 0.17 tex and a content of weakly crosslinked cation exchanger of 6% by mass, based on the cellulose content. These fibers are loaded according to Example 1 with silver ions. The fiber parameters are listed in Table 3.
- Example 3 Fibers are produced according to Example 1 with a titer of 0.5 tex and a content of weakly crosslinked cation exchanger of 0.5% by mass, based on the cellulose content.
- the loading with silver ions is carried out analogously to Example 1.
- the fiber parameters are shown in Table 3. In Table 3, a fiber without a weakly crosslinked cation exchanger was included for comparison.
- Example 4 (Comparative Example) To a cellulose mash in 60% aqueous N-methylmorpholine N-oxide is added an aqueous suspension of a weakly acidic macroporous cation exchanger based on a styrene-divinylbenzene copolymer with chelating iminodiacetic acid groups in such a concentration that the Spun fibers contain a content of 6% by mass based on the cellulose content. The fibers are washed after spinning and loaded as described in Example 1 with silver ions. Table 4 contains the fiber parameters.
- Example 5 Working analogously to Example 4 and gives the mash 6% by mass of a weak acid macroporous cation exchanger based on crosslinked polyacrylate in the sodium form, so that in the spun fiber 6% by mass related ion exchanger are included in the cellulose content, this fiber washes and charged with silver ions as described in Example 1, to give a fiber with 13.6 g Ag / kg fiber. It is surprisingly clear from example 5 that the polyacrylate-based ion exchanger absorbs less than half of silver ions than the slightly crosslinked polyacrylate-based cation exchanger.
- Example 6 Fibers with weakly crosslinked cation exchangers as well as conventional prior art ion exchanges prepared according to Examples 1 to 5 were loaded with silver, cupric and zinc ions. The results are shown in Table 5.
- Fibers loaded with copper ions, silver ions or with a combination of silver and zinc ions can be used as bactericidal fibers.
- Example 7 To a 11% by mass cellulose solution in N-methylmorpholine N-oxide monohydrate is added a suspension of a weakly crosslinked cation exchanger based on a crosslinked copolymer of acrylic acid and sodium acrylate and a strong base anion exchanger based on a styrene-divinylbenzene copolymer with trialkylammonium groups in chloride form in 85% N-methylmorpholine-N-oxide in such a concentration that the spinning solution 11 % By mass of cellulose and, based on the cellulose content, 8% by mass of the weakly crosslinked cation exchanger and 8% by mass of the anion exchanger.
- the spinning solution according to Example 1 is spun with a titer of 0.5 tex.
- the fibers have a tenacity of 26.3 cN / tex, an elongation of 12.1% and a fineness-related loop tearing force of 8.6 cN / tex.
- the silver loading is 52.4 g silver / kg fiber and the loading with benzoate is 16.6 g benzoate / kg fiber. These fibers have a very strong bactericidal action.
- the example demonstrates the suitability of the fibers of the present invention for combined use with prior art anion exchange and cation exchange loaded fibers.
- Example 8 Inventive ion exchanger fibers or films with incorporated cation exchangers prepared according to Example 2 are loaded with nicotine. The loaded fibers or films are washed and dried. These fibers or films can be processed into textile depots and used as transdermal therapeutic systems.
- Fibers prepared according to Example 1 were tested for their bactericidal action in accordance with the European Pharmacopaeia (EP 2002), Chapter 2.6.12, Bioburden determination.
- Papers containing fibers according to Example 1 were tested in an amount such that a gradation of the silver contents in the paper was 190 mg Ag / kg, 760 mg Ag / kg and 3800 mg Ag / kg paper.
- the test was carried out on the following microorganisms (Tables 6 - 9): Pseudomonas aeruginosa ATCC 9027 Staphylococcus aureus ATCC 6538 Bacillus subtilis spores ATCC 6633 Fusarium solani spores ATCC 36031.
- Example 10 Fibers made according to Example 1 were spun with cotton into stocking yarn having a denier Nm 68/1 and a silver content of 1300 mg Ag / kg yarn. From this yarn, a knitted tube was made and tested for bactericidal action (sample 31444083). The test was carried out in accordance with SN195924. The test organism was Lactobacillus brevis DSM 20054. The control sample used was non-antimicrobial cotton fabric (Table 10). In each case 5 measurements were carried out on the basis of the same sample material and the control sample.
- the 24-hour value of the growth control (control or standard tissue) must be at least two orders of magnitude above the initial value (AE ⁇ -2).
- An antimicrobial effect is given when a KBE value is at most 0.5 decimal logarithms above the mean of the zero-contact time CFU values, ie AE 524 > -0.5.
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Abstract
Description
Cellulosische Formkörper mit funktionaler Wirkung sowie Verfahren zu deren HerstellungCellulosic molded bodies with functional action and process for their preparation
Die Erfindung betrifft einen cellulosischen Formkörper sowie ein Verfahren zur Herstellung von cellulosischen Formkörpern nach dem Trocken- Nassextrusionsverfahren mit verbesserten und erweiterten funktionalen Wirkungen insbesondere für den Einsatz in der Medizin, Hygiene, Bekleidung, der Papierherstellung und der Verpackungsindustrie.The invention relates to a cellulosic molding and to a process for producing cellulosic moldings by the dry-wet extrusion process with improved and extended functional effects, in particular for use in medicine, hygiene, clothing, papermaking and the packaging industry.
Die funktionale Wirkung bezieht sich dabei auf eine gleichmäßige und feindosierbare bakterizide Wirkung, insbesondere bei Wundauflagen, Sport- und Freizeitbekleidung, Krankenhaustextilien, Filter- und Verpackungspapieren.The functional effect relates to a uniform and finely dosed bactericidal action, especially in wound dressings, sports and leisure clothing, hospital textiles, filter and packaging papers.
Stand der TechnikState of the art
Es ist bekannt, dass Schwermetallionen wie z. B. Silber-, Quecksilber-, Kupfer-, Zink- und Zirkoniumionen auf Mikroorganismen wie Bakterien, Viren, Pilze und Sporen abtötend oder wachstumshemmend wirken (Thurman et. al., CRC Crit. Rev. In Environ. Contr. 18 (4), S. 295-315 (1989)). Für eine bakterizide Wirkung sind die Silberionen von besonderem Interesse. Der entscheidende Vorteil von Silberionen gegenüber anderen bakterizid wirkenden Metallionen, wie z. B. Hg2+, ist die weitestgehende Unempfindlichkeit des menschlichen Metabolismus gegenüber Silber. Die bakterizid wirkende Konzentration wird bei Silber mit 0,01 - 1 mg/l angegeben (Ullman's Encyclopedia of Industrial Chemistry (5. Aufl.), VCH 1993, Volume A 24, S. 160).It is known that heavy metal ions such. For example, silver, mercury, copper, zinc and zirconium ions have a killing or growth-inhibiting effect on microorganisms such as bacteria, viruses, fungi and spores (Thurman et al., CRC Crit Rev. In Environ. Contr. 18 (4) , Pp. 295-315 (1989)). For a bactericidal effect, the silver ions are of particular interest. The decisive advantage of silver ions over other bactericidal metal ions, such. B. Hg 2+ , is the most insensitive human metabolism to silver. The bactericidal concentration is given as 0.01- 1 mg / L in silver (Ullman's Encyclopedia of Industrial Chemistry (5th ed.), VCH 1993, Volume A 24, p. 160).
Diese Wirkung der Silberionen wird seit langem in den unterschiedlichsten Anwendungen genutzt. Bei der Herstellung von textilen Fasern wird Silber z. B. galvanisch auf der Oberfläche von Polyamidseide abgelagert. Die Verarbeitung von galvanisch versilberter Polyamidseide auf Strick- und Wirkmaschinen ist problematisch, da sich an den Fadenleitorganen teilweise die Silberschicht von der Polyamidseide ablagert und damit zu häufigen Maschinenstillständen führt. Eine weitere bekannte Möglichkeit ist das Einbringen von metallischem Silber, Silber-Zeolith oder Silberglaskeramik in die Fasermatrix von schmelzegesponnenen Fasern wie Polypropylenfasern, Polyesterfasern und Polyamidfasern (Taschenbuch für die Textilindustrie 2003, Schiele & Schön Berlin, S. 124 ff).This effect of silver ions has long been used in a wide variety of applications. In the production of textile fibers silver is z. B. deposited galvanically on the surface of polyamide silk. The processing of electroplated polyamide silk on knitting and knitting machines is problematic, since at the Fadenleitorganen partially deposits the silver layer of the polyamide silk and thus leads to frequent machine downtime. Another known Possibility is the introduction of metallic silver, silver zeolite or silver glass ceramic in the fiber matrix of melt-spun fibers such as polypropylene fibers, polyester fibers and polyamide fibers (Taschenbuch fur den Textilindustrie 2003, Schiele & Schön Berlin, p. 124 ff).
Auch für Acrylfasern wurde der Einsatz von Silber-Zeolith und Silberglaskeramik vorgeschlagen. Auch cellulosische Fasern mit bakteriostatischen oder bakteriziden Eigenschaften sind am Markt. Durch Inkorporieren von Triclosan (2,4,4-Trichloro(ll)- hydroxyphenyläther) in cellulosische Fasern erhält man eine permanent bakteriostatische Faser (ITB International Textile Bulletin 3/2002). Diese Substanz ist wirksam gegen Bakterien, die üblicherweise auf der Haut vorkommen, einschließlich krankheitserregender Staphylococcus-Arten.The use of silver zeolite and silver glass ceramic has also been proposed for acrylic fibers. Cellulosic fibers with bacteriostatic or bactericidal properties are also on the market. By incorporating triclosan (2,4,4-trichloro (II) hydroxyphenyl ether) into cellulosic fibers, a permanent bacteriostatic fiber is obtained (ITB International Textile Bulletin 3/2002). This substance is effective against bacteria commonly found on the skin, including pathogenic Staphylococcus species.
In der DE 10 140772 wird ein Verfahren zur Herstellung von cellulosischen Formkörpern mit inkorporierten Algen beschrieben. Die Formkorper sind in der Lage, aus schwermetallhaltigen Medien Metalle zu adsorbieren. Die schwermetallbeladenen Formkörper können als antibakterielles und/oder fungizides Material verwendet werden. Der Gehalt dieser cellulosischen Formkörper an adsorbierten Schwermetallen ist mindestens mit etwa 70 mg/kg, bezogen auf das Gesamtgewicht des cellulosischen Formkörpers, angegeben.In DE 10 140772 a process for the production of cellulosic moldings with incorporated algae is described. The moldings are capable of adsorbing metals from heavy metal-containing media. The heavy metal loaded moldings can be used as antibacterial and / or fungicidal material. The content of adsorbed heavy metals in these cellulosic moldings is at least about 70 mg / kg, based on the total weight of the cellulosic molding.
Es wird weiter ausgeführt, dass durch Tauchen einer Faser mit einem Braunalgengehalt bezogen auf das Gewicht der Faser von 11,39 Masse-% in eine 0,05 M AgN03-Lösung ein Silbergehalt von 1855 mg/kg Faser erreicht wurde. Da Algen Naturprodukte sind, schwanken die relativ begrenzten Bindungskapazitäten für Schwermetalle. Bei der Bindung von Schwermetallen an Algen spielen unterschiedliche Bindungsmechanismen wie lonentausch, Komplexierung und andere nicht bekannte Reaktionen eine Rolle. Die Bindung der Schwermetalle an den Algen ist deshalb unspezifisch. Ein weiterer Nachteil dieser Faser ist, dass diese nur Kationen für eine bakterizide Wirkung nutzen können und keine bakteriziden Anionen wie z. B. Benzoesäure und Sorbinsäure.It is further stated that by dipping a fiber having a brown algae content, based on the weight of the fiber, of 11.39 mass% into a 0.05 M AgN0 3 solution, a silver content of 1855 mg / kg fiber was achieved. Since algae are natural products, the relatively limited binding capacities for heavy metals vary. Different binding mechanisms such as ion exchange, complexation and other unknown reactions play a role in the binding of heavy metals to algae. The binding of heavy metals to the algae is therefore unspecific. Another disadvantage of this fiber is that they can only use cations for a bactericidal effect and no bactericidal anions such. B. benzoic acid and sorbic acid.
Aufgabe der Erfindung Der Erfindung liegt die Aufgabe zugrunde, einen cellulosischen Formkörper sowie ein Verfahren zur Herstellung von cellulosischen Formkörpern mit funktionaler Wirkung insbesondere für den Einsatz in der Medizin, Hygiene und Bekleidung bereitzustellen, der eine bakterizide Wirkung zeigt und diese insbesondere mit den Vorteilen eines atmungsaktiven Kleidungsstückes verbindet. Eine weitere Aufgabe besteht darin, die Wirkstoffe in einem textilen Depot vorzuhalten und für eine ausreichende Abgabe dieser Stoffe aus dem Depot über die Zeit zu sorgen. Die abzugebende Wirkstoffkonzentration soll regelbar sein. Des weiteren sollen die nach dem erfindungsgemäßen Verfahren hergestellten Formkörper, insbesondere Fasern und Folien, so geschaffen werden, dass sie aufgrund ihres hohen Adsorptionsvermögens an Wirkstoffen zur Herstellung als Wundauflagen, Pflaster, Hygieneartikel, Textilien, Spezialpapiere und als Verpackungsmaterial geeignet sind. Schließlich sollen Verbundstoffe aus Mischungen mit anderen Faserstoffen herstellbar sein.Object of the invention The invention has for its object to provide a cellulosic molded body and a method for the production of cellulosic moldings having a functional effect, especially for use in medicine, hygiene and clothing, which shows a bactericidal effect and this particular connects with the advantages of a breathable garment. Another object is to provide the active ingredients in a textile depot and to ensure a sufficient release of these substances from the depot over time. The drug concentration to be delivered should be controllable. Furthermore, the shaped bodies produced by the process according to the invention, in particular fibers and films, are to be created in such a way that they are suitable for production as wound dressings, patches, hygiene articles, textiles, specialty papers and as packaging material due to their high adsorption capacity. Finally, composites of mixtures with other fibers should be produced.
Weitere Vorteile ergeben sich aus der folgenden Beschreibung.Further advantages will become apparent from the following description.
Diese Aufgabe wird bei dem eingangs genannten Verfahren erfindungsgemäß dadurch gelöst, indem man cellulosische Formkörper, die nach dem Trocken- Nassextrusionsverfahren ersponnen wurden und inkorporierte lonentauscher enthalten mit kationenaktiven oder anionenaktiven Wirkstoffen belädt. Überraschenderweise wurde gefunden, dass die Bindungskapazität für die genannten Wirkstoffe entscheidend vom Vernetzungsgrad der lonentauscher abhängt. So kann die Bindungskapazität für kationenaktive Wirkstoffe, wie __. B. Silber, um mehr als das Doppelte erhöht werden, wenn man Polyacrylate einsetzt, die mit einem mehrfunktionellen Vernetzer schwach vernetzt wurden.This object is achieved according to the invention in the process mentioned above by loading cellulosic moldings spun by the dry-wet extrusion process and incorporating incorporated ion exchanger loaded with cationic or anionic active ingredients. Surprisingly, it has been found that the binding capacity for the active substances mentioned depends crucially on the degree of crosslinking of the ion exchangers. Thus, the binding capacity for cationic active ingredients, such as __. For example, silver can be more than doubled using polyacrylates that have been lightly crosslinked with a multifunctional crosslinker.
Schwach vernetzte lonentauscher im Sinne der vorliegenden Erfindung sind Ionenaustauscher die mit einem verringerten Anteil an Vernetzern versehen sind. Herkömmliche lonenaustauscherharze weisen einen Vernetzeranteil von 4 bis 12 Gew%, bezogen auf die Masse des Austauscherharzes, auf. Schwach vernetzte Ionenaustauscher im Sinne der vorliegenden Erfindung weisen einen Vernetzeranteil von 0,1 bis 2,0 Gew%, bevorzugt 0,3 bis 1 ,5 Gew%, besonders bevorzugt 0,5 bis 1 ,2 Gew% auf. Schwach vernetzte lonenaustauscherharze zeichnen sich auch dadurch aus, dass sie in wässrigen Lösungen sehr stark quellen. Übliche lonenaustauscherharze mit den oben genannten Vernetzeranteilen weisen nur geringe Quellungsgrade auf.Weakly crosslinked ion exchangers for the purposes of the present invention are ion exchangers which are provided with a reduced proportion of crosslinking agents. Conventional ion exchange resins have a crosslinker content of 4 to 12% by weight, based on the mass of the exchange resin. Weakly crosslinked ion exchangers for the purposes of the present invention have a crosslinker content of 0.1 to 2.0% by weight, preferably 0.3 to 1.5% by weight, more preferably 0.5 to 1.2% by weight. Weakly crosslinked ion exchange resins are also characterized by the fact that they swell very strongly in aqueous solutions. Conventional ion exchange resins with the abovementioned crosslinker components have only low degrees of swelling.
Die mit inkorporierten schwach vernetzten Kationentauschern hergestellten Fasern übertreffen mit ihrer Bindungskapazität für Silberionen die der Braunalgen nach der DE 10 140 772 um bis zum 28-fachen. Es ist damit die Möglichkeit gegeben, Fasern oder Folien herzustellen, die z. B. mit kationenaktiven bakteriziden Wirkstoffen wie mit Silberionen hoch beladen werden können. Eine Faser mit 15 Masse-% inkorperiertem schwach vernetzten Kationenaustauscher kann mit ca. 80 g Silber beladen werden. Silberbeladungen der Faser mit > 100 g Ag/kg Faser ist möglich bei entsprechender Erhöhung des Masseanteils des inkorporierten schwach vernetzten Kationenaustauschers.The fibers produced with incorporated weakly crosslinked cation exchangers exceed with their binding capacity for silver ions that of the brown algae according to DE 10 140 772 by up to 28 times. It is thus given the opportunity to produce fibers or films, the z. B. can be highly loaded with cationic bactericidal agents such as silver ions. A fiber with 15% by mass of incorporated weakly crosslinked cation exchanger can be loaded with about 80 g of silver. Silver loading of the fiber with> 100 g Ag / kg fiber is possible with a corresponding increase in the mass fraction of the incorporated weakly crosslinked cation exchanger.
Diese Fasern können dann durch Abmischen mit anderen Fasern, wie z. B. Baumwolle oder synthetischen Fasern auf gewünschte Silbergehalte im herzustellenden Garn gebracht werden. Diese Verfahrensweise lässt eine sehr wirtschaftliche Herstellung von bakterizid wirkenden Garnen zu.These fibers can then be prepared by mixing with other fibers, such as. As cotton or synthetic fibers are brought to desired levels of silver in the yarn to be produced. This procedure allows a very economical production of bactericidal yarns.
Die Inkorporation von Ionenaustauschern führt jedoch mit zunehmendem Anteil in der Faser zu einem nachteiligen Einfluß auf die textil-physikalischen Parameter wie Festigkeit, Dehnung und Schiingenfestigkeit. Insbesondere Festigkeit und Schiingenfestigkeit werden mit zunehmendem Anteil an inkorporiertem Ionenaustauscher in der Faser reduziert.The incorporation of ion exchangers, however, leads to an adverse effect on the textile-physical parameters such as strength, elongation and Schiingenfestigkeit with increasing proportion in the fiber. In particular, strength and loop strength are reduced as the proportion of incorporated ion exchanger in the fiber increases.
Es ist daher auch von wirtschaftlichem Interesse, mit Silber beladene Fasern zu erzeugen, die in ihren textil-physikalischen Eigenschaften, wie Festigkeit und Schiingenfestigkeit, den Eigenschaften nahe kommen, wie sie Fasern aufweisen, die keine inkorporierten Ionenaustauscher enthalten.It is therefore also of economic interest to produce silver-loaded fibers which, in their textile-physical properties, such as strength and sheeting resistance, are close to the properties of fibers containing no incorporated ion exchangers.
Mit der vorliegenden Erfindung ist es möglich Fasern bereitzustellen, die hinsichtlich des Silbergehaltes pro Faser einen ausreichenden Gehalt aufweisen, um eine ausreichende bakterizide Wirkung zu zeigen, jedoch keine Nachteile hinsichtlich der textil- physikalischen Parameter zeigen. Erfindungsgemäß kann mit 0,5 bis 1 ,5 Masse-%, bezogen auf die Cellulosemasse der Faser, an inkorporiertem schwach vernetzten Kationenaustauscher 5000 bis 10.000 mg Ag/kg Faser an die Faser gebunden werden. Derartige Fasern zeigen eine völlig ausreichende bakterizide Wirkung in den bisher bekannten Einsatzgebieten und sind in ihren textil-physikalischen Werten unmodifizierten Fasern ebenbürtig. Die Verarbeitung dieser Fasern und daraus hergestellter Garne ist auf allen Textilmaschinen möglich.With the present invention, it is possible to provide fibers which have a sufficient content in terms of the silver content per fiber to a sufficient level show bactericidal effect, but show no disadvantages in terms of textile-physical parameters. According to the invention, from 0.5 to 1.5 mass%, based on the cellulosic mass of the fiber, of 5000 to 10,000 mg Ag / kg fiber of incorporated weakly crosslinked cation exchanger can be bound to the fiber. Such fibers show a completely sufficient bactericidal action in the hitherto known fields of use and are equal in their textile-physical values to unmodified fibers. The processing of these fibers and yarns made from them is possible on all textile machines.
Setzt man anstelle der schwach vernetzten Kationentauscher lonentauscher auf der Basis von an Acrylsäure-Divinylbenzol-Copolymer gebundenen Carboxylgruppen oder der an Styrol-Divinylbenzol-Copolymergebundenen chelatbildendene Iminodiessigsäure wie in der DE 19 917 614 beschrieben ein, kommt man zu Fasern, die in Bezug auf ihre bakterizide Wirkung vergleichbar sind. Die Aufnahmekapazität für Silberionen beträgt jedoch weniger als 50% der vorgenannten schwach vernetzten Kationentauscher.If, instead of the weakly crosslinked cation exchanger, ion exchangers based on carboxyl groups bonded to acrylic acid-divinylbenzene copolymer or the chelate-forming iminodiacetic acid bound to styrene-divinylbenzene copolymer are used, as described in DE 19 917 614, fibers are obtained which are bactericidal activity are comparable. However, the absorption capacity for silver ions is less than 50% of the aforementioned weakly crosslinked cation exchangers.
Ein Maß für die zu erwartende bakterizide Wirkung der Fasern oder Garne ist die Gleichgewichtskonzentration der Wirkstoffe in wässrigen Lösungen wie z. B. der Silberionen.A measure of the expected bactericidal effect of the fibers or yarns is the equilibrium concentration of the active ingredients in aqueous solutions such. B. the silver ions.
Dazu werden mit Silberionen beladene Fasern oder Garne in destilliertes Wasser mit einer Temperatur von 20°C gelegt und die Gleichgewichtskonzentration der Silberionen nach 24 h gemessen. In der Tabelle 1 sind die Gleichgewichtskonzentrationen an Silberionen und die Beladung der Fasern mit Silber bei Einsatz von schwach vernetzten Kationentauschern und bekannten mit Divinylbenzol vernetzten lonentauschern dargestellt. Man erkennt, dass die Gleichgewichtskonzentration an Silberionen über der für eine bakterizide Wirkung notwendigen Konzentration von 0,01 - 1 mg/l liegt. Die Gleichgewichtskonzentration kann durch Abmischen mit anderen Faserstoffen auf die jeweils erforderliche Konzentration eingestellt werden.For this purpose, loaded with silver ions fibers or yarns are placed in distilled water at a temperature of 20 ° C and measured the equilibrium concentration of the silver ions after 24 h. Table 1 shows the equilibrium concentrations of silver ions and the loading of the fibers with silver using weakly crosslinked cation exchangers and known divinylbenzene crosslinked ion exchangers. It can be seen that the equilibrium concentration of silver ions is above the concentration required for a bactericidal effect of 0.01-1 mg / l. The equilibrium concentration can be adjusted by blending with other fibers to the required concentration.
Tabelle 1: Table 1:
Wie aus Tabelle 1 ersichtlich, wird bei den erfindungsgemäßen Fasern die für den antimikrobiellen Effekt notwendige Gleichgewichtskonzentration erhalten, bei gleichzeitigem höheren Ag-Gehalt der Faser. Die Vorteile hieraus liegen auf der Hand.As can be seen from Table 1, the equilibrium concentration necessary for the antimicrobial effect is obtained with the fibers according to the invention, with a simultaneous higher Ag content of the fiber. The advantages of this are obvious.
In der Anwendung der Fasern werden die freien Ag-Ionen beständig ausgetragen, wobei die Gleichgewichtskonzentration über die Zeit durch das in der Faser deponierte Ag aufrechterhalten wird. Durch die erhöhte Depotwirkung der erfindungsgemäßen Fasern kann somit die Gleichgewichtskonzentration über einen erhöhten Zeitraum aufrechterhalten werden.In the application of the fibers, the free Ag ions are stably discharged, whereby the equilibrium concentration is maintained over time by the Ag deposited in the fiber. Due to the increased depot effect of the fibers according to the invention thus the equilibrium concentration can be maintained over an increased period.
Inkorporiert man in die Faser einen schwach vernetzten Kationentauscher und einen stark basischen Anionenaustauscher auf der Basis von Styrol-Divinylbenzol-Copolymer mit Trialkylammonium-Gruppen in Chlorid-Form, dann kann man die Fasern mit kationenaktiven und anionenaktiven bakterizid wirkenden Ionen beladen, wie z. B. mit Silberionen und Benzoesäure oder Sorbinsäure.If a weakly crosslinked cation exchanger and a strongly basic anion exchanger based on styrene-divinylbenzene copolymer with trialkylammonium groups in chloride form are incorporated into the fiber, then the fibers can be loaded with cation-active and anionically active bactericidal ions, such as, for example, B. with silver ions and benzoic acid or sorbic acid.
Damit ist es möglich, neben dem Einsatz von Silberionen die anionenaktiven Wirkstoffe wie z. B. Benzoesäure und Sorbinsäure einzusetzen. Deren toxikologische Unbedenklichkeit ist in vielen Arbeiten nachgewiesen und deshalb sind sie für den direkten Einsatz in Lebensmitteln zugelassen (Wallhäußer, Sterilisation, Desinfektion, Konservierung (4. Aufl.), Thieme 1988, S. 396). Die Verarbeitung derart ausgerüsteter Fasern in der Papierherstellung oder hergestellter Folien führt zu antimikrobiell aktiven Verpackungen für Lebensmittel. Auch die medizinische Anwendung dieser mit kationenaktiven Wirkstoffen funktionalisierten Fasern sind möglich. So können diese Fasern Wirkstoffe, wie z. B. Nikotin binden. Die Fasern können in Form von Pflastern verarbeitet werden und als transdermale, therapeutische Systeme Anwendung finden.This makes it possible, in addition to the use of silver ions, the anionic active ingredients such. B. benzoic acid and sorbic acid. Their toxicological safety is proven in many works and therefore they are approved for direct use in food (Wallhäußer, sterilization, disinfection, preservation (4th ed.), Thieme 1988, p. 396). The processing of such finished fibers in papermaking or produced films leads to antimicrobial active packaging for food. The medical application of these functionalized with cationic active ingredients fibers are possible. So these fibers can be active ingredients such. B. Nicotine bind. The fibers may be processed in the form of patches and used as transdermal therapeutic systems.
Die Beladung der funktionalisierten Fasern kann zweckmäßigerweise durch Tauchen in einer Lösung mit den entsprechenden Ionen geschehen. Das Tauchen kann dabei sowohl im Batchbetieb als auch kontinuierlich erfolgen. Beim kontinuierlichen Tauchen wird vorzugsweise die geschnittene Faser in einem separaten Bad bei der Nachbehandlung beladen.The loading of the functionalized fibers may conveniently be done by dipping in a solution with the appropriate ions. Diving can be done both in batch mode and continuously. In continuous dipping, preferably the cut fiber is loaded in a separate bath in the after-treatment.
Zur weiteren Verdeutlichung der Erfindung und ihrer wesentlichen Eigenschaften dienen die folgenden Beispiele:To further illustrate the invention and its essential characteristics, the following examples serve:
Beispiel 1example 1
Einer 12 Masse-%igen Celluloselösung in N-Methylmorpholin-N-Oxid-Monohydrat wird ein pulverförm iger schwach vernetzter Kationentauscher auf der Basis eines vernetzten Copolymerisates aus Acrylsäure und Natriumacrylat mit einer Korngröße < 10 μm in einem Gewichtsanteil von 15 Masse-%, bezogen auf einen Celluloseanteil, zugesetzt. Diese Spinnlösung wird in einem Kneter homogenisiert und bei einer Temperatur von ca. 90°C durch eine Spinndüse mit 480 Löchern und einem Düsenlochdurchmesser von 80 μm gesponnen. Die Abzugsgeschwindigkeit liegt bei 30 m/min. Der multifile Faden wird durch mehrere Waschbäder geführt zur Auswaschung des N-Methylmorpholin-N- Oxides. Die Fasern werden abgeschleudert und mit 10 Liter einer 0,1 M Silbernitratlösung pro kg Fasermaterial beladen. Nach der Beladung werden die Fasern geschleudert und von anhaftendem Silbernitrat freigewaschen. Anschließend werden die Fasern bei ca. 80°C getrocknet.A 12% by mass cellulose solution in N-methylmorpholine N-oxide monohydrate is a powdered weakly crosslinked cation exchanger based on a crosslinked copolymer of acrylic acid and sodium with a particle size <10 microns in a weight fraction of 15% by mass to a cellulose content added. This spinning solution is homogenized in a kneader and spun at a temperature of about 90 ° C through a spinneret with 480 holes and a nozzle hole diameter of 80 microns. The take-off speed is 30 m / min. The multifilament yarn is passed through several washing baths to leach the N-methylmorpholine-N-oxide. The fibers are spun off and loaded with 10 liters of a 0.1 M silver nitrate solution per kg of fiber material. After loading, the fibers are spun and washed free from adhering silver nitrate. Subsequently, the fibers are dried at about 80 ° C.
Tabelle 2:Table 2:
Feinheit dtex 0,7Fineness dtex 0.7
Feinheitsbezogene Reißkraft trocken cN/tex 22,5 Dehnung trocken % 14,8Fineness-based tensile strength dry cN / tex 22.5 Elongation dry% 14.8
Feinheitsbezogene Schlingenreißkraft cN/tex 7,5Fineness-related loop tear force cN / tex 7,5
Silbergehalt g/kg Faser 80Silver content g / kg fiber 80
Tabelle 2 zeigt die Faserparameter und den Silbergehalt der Faser. Eine so hoch beladene Faser hat den Vorteil, dass durch Verschneiden der Faser mit anderen textilen Fasern wie z. B. Baumwolle sehr wirtschaftlich silberhaltige Garne hergestellt werden können. Bei einem Gehalt von ca. 5000 mg Ag/kg Garn kann die Silberfaser um das 16- fache verschnitten werden.Table 2 shows the fiber parameters and the silver content of the fiber. Such a highly loaded fiber has the advantage that by blending the fiber with other textile fibers such. B. cotton very economical silver-containing yarns can be produced. At a content of about 5000 mg Ag / kg of yarn, the silver fiber can be cut 16 times.
Auf diese Weise hergestellte Garne lassen sich auf Strick- und Wirkmaschinen im Gegensatz zu galvanisierten Polyamidfäden sehr gut verarbeiten.Yarns produced in this way can be processed very well on knitting and knitting machines, in contrast to galvanized polyamide threads.
Beispiel 2 Fasern werden nach Beispiel 1 ersponnen mit einem Titer von 0,17 tex und einem Gehalt an schwach vernetztem Kationentauscher von 6 Masse-%, bezogen auf den Celluloseanteil. Diese Fasern werden nach Beispiel 1 mit Silberionen beladen. Die Faserparameter sind in Tabelle 3 aufgeführt.Example 2 Fibers are spun according to Example 1 with a titer of 0.17 tex and a content of weakly crosslinked cation exchanger of 6% by mass, based on the cellulose content. These fibers are loaded according to Example 1 with silver ions. The fiber parameters are listed in Table 3.
Beispiel 3 Fasern werden nach Beispiel 1 hergestellt mit einem Titer von 0,5 tex und einem Gehalt an schwach vernetztem Kationentauscher von 0,5 Masse-%, bezogen auf den Celluloseanteil. Die Beladung mit Silberionen wird analog Beispiel 1 vorgenommen. Die Faserparameter sind der Tabelle 3 zu entnehmen. In die Tabelle 3 wurde eine Faser ohne schwach vernetzten Kationentauscher zum Vergleich aufgenommen.Example 3 Fibers are produced according to Example 1 with a titer of 0.5 tex and a content of weakly crosslinked cation exchanger of 0.5% by mass, based on the cellulose content. The loading with silver ions is carried out analogously to Example 1. The fiber parameters are shown in Table 3. In Table 3, a fiber without a weakly crosslinked cation exchanger was included for comparison.
Tabelle 3:Table 3:
Aus den Beispielen 1 - 3 ist zu entnehmen, dass der Silbergehalt auf der Faser mit dem Gehalt des schwach vernetzten Kationentauschers in weiten Grenzen einstellbar ist. Selbst mit 0,5 Masse-% kann noch ein hoher Silbergehalt erreicht werden. Der Einfluss von 0,5 Masse-% des schwach vernetzten Kationentauschers auf die textilen Faserparameter ist unwesentlich.It can be seen from Examples 1 to 3 that the silver content on the fiber can be adjusted within wide limits with the content of the weakly crosslinked cation exchanger. Even with 0.5% by mass, a high silver content can still be achieved. The influence of 0.5% by mass of the weakly crosslinked cation exchanger on the textile fiber parameters is insignificant.
Beispiel 4 (Vergleichsbeispiel) Einer Cellulosemaische in 60%-igem wässrigen N-Methylmorpholin-N-Oxid wird eine wässrige Suspension eines schwachsauren makroporösen Kationentauschers auf der Basis eines Styrol-Divinylbenzol-Copolymer mit chelatbildenden Iminodiessigsäure- Gruppen in einer solchen Konzentration zugegeben, dass die ersponnenen Fasern einen Gehalt von 6 Masse-% bezogen auf den Celluloseanteil enthalten. Die Fasern werden nach dem Ausspinnen gewaschen und wie im Beispiel 1 beschrieben mit Silberionen beladen. Tabelle 4 enthält die Faserparameter.Example 4 (Comparative Example) To a cellulose mash in 60% aqueous N-methylmorpholine N-oxide is added an aqueous suspension of a weakly acidic macroporous cation exchanger based on a styrene-divinylbenzene copolymer with chelating iminodiacetic acid groups in such a concentration that the Spun fibers contain a content of 6% by mass based on the cellulose content. The fibers are washed after spinning and loaded as described in Example 1 with silver ions. Table 4 contains the fiber parameters.
Tabelle 4:Table 4:
Beispiel 5 (Vergleichsbeispiel)Example 5 (Comparative Example)
Arbeitet man analog Beispiel 4 und gibt der Maische 6 Masse-% eines schwachsauren makroporösen Kationentauschers auf der Basis von vernetztem Polyacrylat in der Natrium-Form zu, so dass in der ersponnenen Faser 6 Masse-% lonentauscher bezogen auf den Celluloseanteil enthalten sind, wäscht diese Faser und belädt sie mit Silberionen wie in Beispiel 1 beschrieben, so erhält man eine Faser mit 13,6 g Ag/kg Faser. Am Beispiel 5 wird überraschend deutlich, dass der lonentauscher auf Polyacrylatbasis weniger als die Hälfte an Silberionen aufnimmt als der schwach vernetzte Kationentauscher auf Polyacrylatbasis. Die Steigerung der Bindungskapazität um mehr als 100% bringt deutliche technologische und wirtschaftliche Vorteile dadurch, dass mit geringen Mengen schwach vernetzten Kationentauschern in der Faser die textil- physikalischen Parameter kaum beeinflusst werden, andererseits durch die hohe Aufnahme an Silberionen durch das Verschneiden mit anderen Fasern sehr wirtschaftlich gearbeitet werden kann.Working analogously to Example 4 and gives the mash 6% by mass of a weak acid macroporous cation exchanger based on crosslinked polyacrylate in the sodium form, so that in the spun fiber 6% by mass related ion exchanger are included in the cellulose content, this fiber washes and charged with silver ions as described in Example 1, to give a fiber with 13.6 g Ag / kg fiber. It is surprisingly clear from example 5 that the polyacrylate-based ion exchanger absorbs less than half of silver ions than the slightly crosslinked polyacrylate-based cation exchanger. Increasing the binding capacity by more than 100% brings significant technological and economic advantages in that the small particles of weakly crosslinked cation exchangers in the fiber hardly affect the textile-physical parameters, and on the other hand by the high uptake of silver ions by blending with other fibers can be worked economically.
Beispiel 6 Fasern mit schwach vernetzten Kationentauschern sowie herkömmlichen lonenaustauschen nach dem Stande der Technik, hergestellt nach den Beispielen 1 bis 5 wurden mit Silber-, Kupfer (II)- und Zinkionen beladen. Die Ergebnisse sind in der Tabelle 5 aufgeführt.Example 6 Fibers with weakly crosslinked cation exchangers as well as conventional prior art ion exchanges prepared according to Examples 1 to 5 were loaded with silver, cupric and zinc ions. The results are shown in Table 5.
Tabelle 5:Table 5:
Fasern beladen mit Kupferionen, Silberionen oder mit einer Kombination aus Silber- und Zinkionen können als bakterizide Fasern eingesetzt werden.Fibers loaded with copper ions, silver ions or with a combination of silver and zinc ions can be used as bactericidal fibers.
Beispiel 7 Einer 11 Masse-%igen Celluloselösung in N-Methylmorpholin-N-Oxid-Monohydrat wird eine Suspension eines schwach vernetzten Kationentauschers auf der Basis eines vernetzten Copolymerisates aus Acrylsäure und Natriumacrylat und eines stark basischen Anionentauschers auf der Basis eines Styrol-Divinylbenzol-Copolymer mit Trialkylammonium-Gruppen in Chlorid-Form in 85%-igem N-Methylmorpholin-N-Oxid in einer solchen Konzentration zugegeben, dass die Spinnlösung 11 Masse-% Cellulose und bezogen auf den Celluloseanteil 8 Masse-% des schwach vernetzten Kationentauschers und 8 Masse-% des Anionentauschers enthält. Nach dem Homogenisieren wird die Spinnlösung nach Beispiel 1 mit einem Titer von 0,5 tex versponnen. Die Fasern haben eine Festigkeit von 26,3 cN/tex, eine Dehnung von 12,1% und eine feinheitsbezogene Schlingenreißkraft von 8,6 cN/tex.Example 7 To a 11% by mass cellulose solution in N-methylmorpholine N-oxide monohydrate is added a suspension of a weakly crosslinked cation exchanger based on a crosslinked copolymer of acrylic acid and sodium acrylate and a strong base anion exchanger based on a styrene-divinylbenzene copolymer with trialkylammonium groups in chloride form in 85% N-methylmorpholine-N-oxide in such a concentration that the spinning solution 11 % By mass of cellulose and, based on the cellulose content, 8% by mass of the weakly crosslinked cation exchanger and 8% by mass of the anion exchanger. After homogenization, the spinning solution according to Example 1 is spun with a titer of 0.5 tex. The fibers have a tenacity of 26.3 cN / tex, an elongation of 12.1% and a fineness-related loop tearing force of 8.6 cN / tex.
Die Silberbeladung liegt bei 52,4 g Silber/kg Faser und die Beladung mit Benzoat bei 16,6 g Benzoat/kg Faser. Diese Fasern besitzen eine sehr starke bakterizide Wirkung. Das Beispiel zeigt die Eignung der erfindungsgemäßen Fasern zur kombinierten Anwendung mit Anionenaustauschern und Kationenaustauschern beladenen Fasern nach dem Stande der Technik.The silver loading is 52.4 g silver / kg fiber and the loading with benzoate is 16.6 g benzoate / kg fiber. These fibers have a very strong bactericidal action. The example demonstrates the suitability of the fibers of the present invention for combined use with prior art anion exchange and cation exchange loaded fibers.
Beispiel 8 Erfindungsgemäße lonentauscherfasem oder -folien mit inkorporierten Kationentauschern hergestellt nach Beispiel 2 werden mit Nikotin beladen. Die beladenen Fasern oder Folien werden gewaschen und getrocknet. Diese Fasern oder Folien können zu textilen Depots verarbeitet werden und als transdermale, therapeutische Systeme zur Anwendung kommen.Example 8 Inventive ion exchanger fibers or films with incorporated cation exchangers prepared according to Example 2 are loaded with nicotine. The loaded fibers or films are washed and dried. These fibers or films can be processed into textile depots and used as transdermal therapeutic systems.
Beispiel 9Example 9
Fasern, nach Beispiel 1 hergestellt, wurden auf ihre bakterizide Wirkung in Anlehnung an die European Pharmacopaeia (EP 2002), Chapter 2.6.12, Bioburden determination geprüft.Fibers prepared according to Example 1 were tested for their bactericidal action in accordance with the European Pharmacopaeia (EP 2002), Chapter 2.6.12, Bioburden determination.
Geprüft wurden Papiere, die Fasern nach Beispiel 1 enthalten, in einer Menge, dass eine Abstufung der Silbergehalte im Papier vorlagen von 190 mg Ag/kg, 760 mg Ag/kg und 3800 mg Ag/kg Papier. Die Prüfung wurde an folgenden Mikroorganismen vorgenommen (Tabellen 6 - 9): Pseudomonas aeruginosa ATCC 9027 Staphylococcus aureus ATCC 6538 Bacillus subtilis spores ATCC 6633 Fusarium solani spores ATCC 36031.Papers containing fibers according to Example 1 were tested in an amount such that a gradation of the silver contents in the paper was 190 mg Ag / kg, 760 mg Ag / kg and 3800 mg Ag / kg paper. The test was carried out on the following microorganisms (Tables 6 - 9): Pseudomonas aeruginosa ATCC 9027 Staphylococcus aureus ATCC 6538 Bacillus subtilis spores ATCC 6633 Fusarium solani spores ATCC 36031.
Tabelle 6 - Pseudomonas aeruginosaTable 6 - Pseudomonas aeruginosa
Tabelle 9 - Bacillus subtilis sporesTable 9 - Bacillus subtilis spores
Alle Messergebnisse der Keimzahlen der Tabellen 6 bis 9 sind mit einem Messfehler von 10% behaftet. Die Vergleichsprobe war ein Papier ohne silberhaltige Fasern. Für alle Testkeime konnten Abhängigkeiten der mikrobioziden Wirkung im Hinblick auf Einwirkungsdauer und Konzentration der Silberbeladung nachgewiesen werden. Erwartungsgemäß zeigten die Bacillus subtilis spores die größte Resistenz. Aber auch bei diesen konnte eine Absenkung der Keime erzielt werden.All measurement results of the germ counts in Tables 6 to 9 are subject to a measurement error of 10%. The comparative sample was a paper without silver-containing fibers. Dependencies of the microbicidal activity with regard to exposure time and concentration of the silver loading could be detected for all test germs. As expected, Bacillus subtilis spores showed the highest resistance. But even with these a lowering of the germs could be achieved.
Beispiel 10 Fasern, hergestellt nach Beispiel 1, wurden mit Baumwolle zu Strumpfgarn mit einem Titer Nm 68/1 und einem Silbergehalt von 1300 mg Ag/kg Garn versponnen. Aus diesem Garn wurde ein Strickschlauch gefertigt und auf bakterizide Wirkung geprüft (Probe 31444083). Die Prüfung erfolgte in Anlehnung an SN195924. Der Testorganismus war Lactobacillus brevis DSM 20054. Als Kontrollprobe wurde ein nicht antimikrobiell ausgerüstetes Baumwollgewebe eingesetzt (Tabelle 10). Es wurden jeweils 5 Messungen anhand des gleichen Probenmaterials sowie der Kontrollprobe durchgeführt.Example 10 Fibers made according to Example 1 were spun with cotton into stocking yarn having a denier Nm 68/1 and a silver content of 1300 mg Ag / kg yarn. From this yarn, a knitted tube was made and tested for bactericidal action (sample 31444083). The test was carried out in accordance with SN195924. The test organism was Lactobacillus brevis DSM 20054. The control sample used was non-antimicrobial cotton fabric (Table 10). In each case 5 measurements were carried out on the basis of the same sample material and the control sample.
Tabelle 10 - Ergebnisse der Prüfung der antibakteriellen Wirkung im Keimträgerversuch am Prüfkeim Lactobacillus brevis.Table 10 - Results of the test of antibacterial activity in the germ carrier test on the test bacterium Lactobacillus brevis.
KBE = Zahl der koloniebildenden Einheiten des Testbakteriums AE = antimikrobieller EffektCFU = number of colony-forming units of the test bacterium AE = antimicrobial effect
Bewertungskriterien: Der 24-Stunden-Wert der Wachstumskontrolle (Kontroll-, bzw. Standardgewebe) muss mindestens um zwei Zehnerpotenzen über dem Anfangswert liegen (AE < -2). Eine antimikrobielle Wirkung ist dann gegeben, wenn ein KBE-Wert höchstens 0,5 dekadische Logarithmen über dem Mittelwert der KBE-Werte zur Nullkontaktzeit liegt, d. h. AE524 > -0,5 ist.Evaluation criteria: The 24-hour value of the growth control (control or standard tissue) must be at least two orders of magnitude above the initial value (AE <-2). An antimicrobial effect is given when a KBE value is at most 0.5 decimal logarithms above the mean of the zero-contact time CFU values, ie AE 524 > -0.5.
Die Wirkung einer antimikrobiellen Ausrüstung ist gegeben, wenn für den Testkeim wenigstens 4 von 5 KBE-Einzelwerte jeder Kontaktzeit antimikrobielle Wirkung zeigen. Diese Anforderungen erfüllt nach den Testergebnissen die Probe Nr.: 3144408: Strickschlauch. The effect of antimicrobial equipment is given when at least 4 out of 5 CFU individual values of each contact time have antimicrobial activity for the test germ. According to the test results, these requirements are met by sample No .: 3144408: Knitting hose.
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| DE102006056977B3 (en) | 2006-11-30 | 2008-05-08 | Smart Fiber Ag | Use of an antimicrobial textile composite as a holder to cause a bacteriostatic effect on the objects and materials to be cleaned in the interior of a washing machine or dishwasher, where the holder comprises fibers with cellulose matrix |
| DE102007012972B4 (en) * | 2007-03-14 | 2010-09-02 | Smart Fiber Ag | Device for the biocidal treatment of laundry |
| DE102007019768A1 (en) * | 2007-04-25 | 2008-11-13 | Thüringisches Institut für Textil- und Kunststoff-Forschung e.V. | A process for producing a high whiteness bioactive cellulosic fiber |
| DE102007054702B4 (en) * | 2007-11-14 | 2018-10-18 | Smartpolymer Gmbh | Process for the preparation of cellulosic shaped bodies, cellulosic shaped bodies and their use |
| DE102009010968A1 (en) | 2009-02-27 | 2010-09-02 | Flockfaser GmbH Thüringen | Antibacterially active flock fibers, for use in electrostatic flocking, are obtained from synthetic and/or natural flock fibers by blending with silver-charged bioactive cellulose fibers |
| CN102220730B (en) * | 2011-04-13 | 2013-08-28 | 成都印钞有限公司 | Silver-zinc zirconium phosphate composite germicide for paper money and preparation method thereof |
| RU2472892C1 (en) * | 2011-10-13 | 2013-01-20 | Леонид Асхатович Мазитов | Method of obtaining bactericidal paper |
| GB2511528A (en) | 2013-03-06 | 2014-09-10 | Speciality Fibres And Materials Ltd | Absorbent materials |
| CN104389245B (en) * | 2014-09-29 | 2016-02-17 | 吉特利环保科技(厦门)有限公司 | A kind of preparation technology of nano Ag antibacterial fiber tableware |
| CN105200844A (en) * | 2015-08-21 | 2015-12-30 | 西南石油大学 | Preparing method for antibacterial disinfecting tissue paper |
| US20220061327A1 (en) * | 2020-08-28 | 2022-03-03 | Uop Llc | Antiviral metal treatments for fiber substrates, filter media having antiviral metal treatments, and processes for treating fiber substrates |
| DE102022109459A1 (en) | 2021-04-21 | 2022-10-27 | Smartpolymer Gmbh | Wash-permanent bioactive cellulose fiber with antibacterial and antiviral properties |
Family Cites Families (19)
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| US6258368B1 (en) * | 1997-06-04 | 2001-07-10 | The Procter & Gamble Company | Antimicrobial wipes |
| DE19805447A1 (en) * | 1998-02-11 | 1999-08-12 | Bayer Ag | Modified superabsorbents based on polyacrylonitrile emulsions |
| US6110533A (en) * | 1998-03-16 | 2000-08-29 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of Natural Resources | Polymeric desiccant articles and process for their manufacture |
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| US6660903B1 (en) * | 1999-10-01 | 2003-12-09 | Kimberly-Clark Worldwide, Inc. | Center-fill absorbent article with a central rising member |
| DE10009471B4 (en) * | 2000-02-28 | 2006-07-27 | Thüringisches Institut für Textil- und Kunststoff-Forschung e.V. | Process for the preparation of a solution of increased thermal stability of cellulose in aqueous amine oxide |
| US6828014B2 (en) * | 2001-03-22 | 2004-12-07 | Kimberly-Clark Worldwide, Inc. | Water-dispersible, cationic polymers, a method of making same and items using same |
| DE10140772A1 (en) * | 2001-08-20 | 2003-03-13 | Zimmer Ag | A process for the removal of heavy metals from heavy metal containing media using a lyocell-shaped body and Lyocell-shaped bodies with adsorbed heavy metals and their use |
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| JP2004123662A (en) * | 2002-10-07 | 2004-04-22 | Lion Corp | Exfoliating sheet |
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- 2004-04-01 JP JP2006504948A patent/JP2006522232A/en active Pending
- 2004-04-01 CN CNB2004800091522A patent/CN100545325C/en not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2004088009A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1816651A (en) | 2006-08-09 |
| RU2340710C2 (en) | 2008-12-10 |
| CN100545325C (en) | 2009-09-30 |
| ATE440981T1 (en) | 2009-09-15 |
| DE10315749A1 (en) | 2004-10-14 |
| PL1611272T3 (en) | 2009-12-31 |
| DE502004009966D1 (en) | 2009-10-08 |
| US20060283567A1 (en) | 2006-12-21 |
| RU2005134210A (en) | 2006-05-10 |
| EP1611272B1 (en) | 2009-08-26 |
| WO2004088009A1 (en) | 2004-10-14 |
| JP2006522232A (en) | 2006-09-28 |
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