CN108823985A - A kind of medical antibacterial quilt cover facilitating filling - Google Patents
A kind of medical antibacterial quilt cover facilitating filling Download PDFInfo
- Publication number
- CN108823985A CN108823985A CN201810700863.8A CN201810700863A CN108823985A CN 108823985 A CN108823985 A CN 108823985A CN 201810700863 A CN201810700863 A CN 201810700863A CN 108823985 A CN108823985 A CN 108823985A
- Authority
- CN
- China
- Prior art keywords
- parts
- antibacterial
- quilt cover
- minutes
- fabric
- 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
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 104
- 238000011049 filling Methods 0.000 title claims abstract description 43
- 239000004744 fabric Substances 0.000 claims abstract description 100
- 230000003115 biocidal effect Effects 0.000 claims abstract description 45
- 238000002360 preparation method Methods 0.000 claims description 45
- 239000000243 solution Substances 0.000 claims description 41
- 238000003756 stirring Methods 0.000 claims description 40
- 239000003242 anti bacterial agent Substances 0.000 claims description 36
- 229920002907 Guar gum Polymers 0.000 claims description 35
- 239000000665 guar gum Substances 0.000 claims description 35
- 235000010417 guar gum Nutrition 0.000 claims description 35
- 229960002154 guar gum Drugs 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 23
- 239000000843 powder Substances 0.000 claims description 23
- 239000007767 bonding agent Substances 0.000 claims description 22
- 238000010792 warming Methods 0.000 claims description 21
- 229920000881 Modified starch Polymers 0.000 claims description 20
- 239000004368 Modified starch Substances 0.000 claims description 20
- 235000019426 modified starch Nutrition 0.000 claims description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- 229920002472 Starch Polymers 0.000 claims description 18
- 239000008107 starch Substances 0.000 claims description 18
- 235000019698 starch Nutrition 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 16
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 16
- 235000019441 ethanol Nutrition 0.000 claims description 15
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 14
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 229940051841 polyoxyethylene ether Drugs 0.000 claims description 13
- 229920000056 polyoxyethylene ether Polymers 0.000 claims description 13
- HZBAVWLZSLOCFR-UHFFFAOYSA-N oxosilane Chemical compound [SiH2]=O HZBAVWLZSLOCFR-UHFFFAOYSA-N 0.000 claims description 12
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 12
- 229920002554 vinyl polymer Polymers 0.000 claims description 12
- 238000005119 centrifugation Methods 0.000 claims description 11
- 238000007598 dipping method Methods 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 229910001570 bauxite Inorganic materials 0.000 claims description 8
- 229910052810 boron oxide Inorganic materials 0.000 claims description 8
- 238000001354 calcination Methods 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 239000013049 sediment Substances 0.000 claims description 8
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 7
- MOWNZPNSYMGTMD-UHFFFAOYSA-N oxidoboron Chemical class O=[B] MOWNZPNSYMGTMD-UHFFFAOYSA-N 0.000 claims description 7
- 239000011787 zinc oxide Substances 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- 241001609073 Neopallasia Species 0.000 claims description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 6
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 6
- 238000002604 ultrasonography Methods 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 150000002191 fatty alcohols Chemical class 0.000 claims description 5
- 229920002401 polyacrylamide Polymers 0.000 claims description 5
- 108010073771 Soybean Proteins Proteins 0.000 claims description 4
- 235000019710 soybean protein Nutrition 0.000 claims description 4
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 claims description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 3
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 239000000908 ammonium hydroxide Substances 0.000 claims description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 3
- DOEHJNBEOVLHGL-UHFFFAOYSA-N trichloro(propyl)silane Chemical compound CCC[Si](Cl)(Cl)Cl DOEHJNBEOVLHGL-UHFFFAOYSA-N 0.000 claims description 3
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 230000008859 change Effects 0.000 claims description 2
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims description 2
- 239000004411 aluminium Substances 0.000 claims 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 2
- 229910052782 aluminium Inorganic materials 0.000 claims 2
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 241000894006 Bacteria Species 0.000 abstract description 14
- 230000000694 effects Effects 0.000 abstract description 11
- 230000000845 anti-microbial effect Effects 0.000 abstract description 8
- 238000005406 washing Methods 0.000 abstract description 6
- 230000004060 metabolic process Effects 0.000 abstract description 4
- 239000008280 blood Substances 0.000 abstract description 3
- 210000004369 blood Anatomy 0.000 abstract description 3
- 230000036039 immunity Effects 0.000 abstract description 3
- 230000002045 lasting effect Effects 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 230000004089 microcirculation Effects 0.000 abstract description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 19
- 238000005516 engineering process Methods 0.000 description 13
- 238000012545 processing Methods 0.000 description 11
- 239000002994 raw material Substances 0.000 description 10
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 10
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 8
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 8
- 229920002338 polyhydroxyethylmethacrylate Polymers 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000000835 fiber Substances 0.000 description 5
- 239000004753 textile Substances 0.000 description 5
- 240000001851 Artemisia dracunculus Species 0.000 description 3
- 238000009395 breeding Methods 0.000 description 3
- 230000001488 breeding effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 210000001520 comb Anatomy 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 210000004243 sweat Anatomy 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 244000126211 Hericium coralloides Species 0.000 description 1
- 241000276489 Merlangius merlangus Species 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 229920004933 Terylene® Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- FYHXNYLLNIKZMR-UHFFFAOYSA-N calcium;carbonic acid Chemical compound [Ca].OC(O)=O FYHXNYLLNIKZMR-UHFFFAOYSA-N 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002068 microbial inoculum Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- ONJQDTZCDSESIW-UHFFFAOYSA-N polidocanol Chemical group CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO ONJQDTZCDSESIW-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012113 quantitative test Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 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
- 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/53—Polyethers
-
- 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
- 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
- D06M11/45—Oxides or hydroxides of elements of Groups 3 or 13 of the Periodic Table; Aluminates
-
- 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
- D06M11/73—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 carbon or compounds thereof
- D06M11/76—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 carbon or compounds thereof with carbon oxides or carbonates
-
- 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
- D06M11/77—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 silicon or compounds thereof
- D06M11/79—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 silicon or compounds thereof with silicon dioxide, silicic acids or their salts
-
- 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
- D06M11/80—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 boron or compounds thereof, e.g. borides
-
- 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
- D06M11/83—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 metals; with metal-generating compounds, e.g. metal carbonyls; Reduction of metal compounds on textiles
-
- 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
- D06M13/50—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms
- D06M13/51—Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond
- D06M13/513—Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond with at least one carbon-silicon bond
- D06M13/5135—Unsaturated compounds containing silicon atoms
-
- 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
-
- 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
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- 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
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/35—Abrasion, pilling or fibrillation resistance
Landscapes
- Textile Engineering (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
The invention discloses a kind of medical antibacterial quilt covers for facilitating filling, are process using antibacterial flexible fabric.The medical antibacterial quilt cover for facilitating filling of the invention, fabric is soft, and elasticity is good, and filling is easy, and unpicks and washes simply, antimicrobial component is added in fabric, antibiotic property is lasting, and antibacterial range is wide, non-stimulated to skin.Still there is good antibacterial effect, anti-fluffing and anti-pilling effect is good after after washing several times.It is used particularly suitable for the environment of hospital or other bacteriums easy to breed, household etc..The medical antibacterial quilt cover for facilitating filling of the invention also has far-infrared health-care effect, can enhance human immunity, cytothesis ability, improves blood microcirculation, boosts metabolism.
Description
Technical field
The present invention relates to medical antibacterial quilt cover technical fields.
Background technique
Quilt cover is enclosed outside the core directly and human contact, the head of a quilt usually can breed bacterium because of reasons such as sweat stain, frictions
And acarid, along with hospital flow of personnel itself is big, bacterium is more, the quilt cover being infected with germs and direct body contact are built
It is unhygienic, also it is easy infected wound.Develop a kind of medical antibacterial quilt cover that can inhibit bacteria breed, soft comfortable, antibacterial bacteriostatic
It is of great significance.
Quilt cover currently on the market mostly makes improvement in flower pattern, in appearance, and the research about antibacterial quilt cover is less.It is medical anti-
Bacterium quilt cover should play kill pathogen, truncation spread of germs approach, prevent bacterium breeding, reduce germ contamination bring it is smelly
The effect of taste.Qualified quilt cover antibacterial fabric needs to have broad-spectrum antiseptic, safe and non-toxic, without any side effects to human body spy
Point.Antibacterial fabric can effectively inhibit the regeneration and breeding of the bacterium, fungi on fabric, remain fabric itself clean.It is anti-
Bacterium fabric is mainly divided to two kinds：1, the fabric of Antibacterial accessory ingredient processing.Antibacterial accessory ingredient is moved to inside fabric by high temperature, quilt after cooling
It is fixed on inside fabric, there is good washability and reliable broad-spectrum antimicrobial effect.2, fabric made of anti-bacterial fibre.Antibacterial
Fabric made of fiber is that chemical fiber plant is added to anti-biotic material in terylene chips when producing polyester fiber, is then melted together
Melt blend spinning.The principle of antibacterial fabric is the cell wall that antimicrobial component destroys bacterium, since osmotic pressure intracellular is extracellular infiltration
20-30 times pressed thoroughly, therefore membranolysis, endochylema beyond the region of objective existence are let out, and also just terminate the metabolic process of microorganism in this way, make micro- life
Object can not grow and breed.Antibacterial fabric can have antibiotic and sterilizing, moldproof, anti-odour, high-strength moisture absorption, ventilative row through processing simultaneously
The functions such as sweat, pro-skin skin care, anion, far infrared health care form natural green environment protection multifunctional textile.Antibacterial quilt cover for
All kinds of bacteriums of harmful to human, the growth and breeding of fungi have extremely strong inhibiting effect, are suitable for various textile fabrics, can assign and knit
The efficient antibacterial and deodouring of object and water-wash resistance.Furthermore medical quilt cover is due to changing clothes frequently, it should have good pliability and bullet
Property, it conveniently changes clothes and loads.
Summary of the invention
The present invention provides a kind of medical antibacterial quilt covers for facilitating filling.The present invention adopts the following technical scheme that：
A kind of medical antibacterial quilt cover facilitating filling：Fabric is antibacterial flexible fabric.Facilitate the medical antibacterial quilt cover of filling
Preparation method be：Antibacterial flexible fabric is cut out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：Fabric is immersed in antibiotic finishing solution, bath raio 1:(5-10),
Dipping temperature is 35-45 DEG C, and dip time is 30-60 minutes, takes out fabric, mangle, pick-up 40%-70%, in 65-80
It is DEG C dry 5-10 hours, 5-10 minutes dry at 115-125 DEG C, obtain antibacterial flexible fabric.
In some embodiments of the invention, the antibiotic finishing solution includes following components in parts by weight：Antibacterial agent 25-35
Part, 0.5-1.5 parts of vinyl front three oxosilane, 0.5-1.5 parts of fatty alcohol polyoxyethylene ether, 80-100 parts of water.
In other embodiments of the invention, the antibiotic finishing solution includes following components in parts by weight：Antibacterial agent 25-
35 parts, 0.5-1.5 parts of vinyl front three oxosilane, 0.5-1.5 parts of fatty alcohol polyoxyethylene ether, 3-5 parts of bonding agent, water 80-
100 parts.
The preparation method of antibiotic finishing solution is：Weigh each raw material by weight, 25-35 DEG C, revolving speed be 300-500 turn/
Minute condition stirs 1-3 hours, obtains antibiotic finishing solution.
In some embodiments of the invention, the preparation method of antibacterial agent is as follows：By 1-3 parts of calcium carbonate, 1.5-3.5 parts of oxygen
Change zinc, 2-6 parts of boron oxides, 5-10 parts of silica whites, 8-12 parts of aluminium oxide, 28-32 parts of bauxite mixing, 240-270 parts of water are added
In, be added tetrabutylammonium hydroxide aqueous solution, 0.3-0.9 parts of TritonX-100 that 0.1-0.5 part mass fractions are 25-40%,
10-20 parts of ethyl alcohol are that 300-800 revs/min of condition stirs 20-60 minutes in 25-35 DEG C, revolving speed, are 20- in ultrasonic frequency
60kHz, power are 300-800W condition ultrasound 20-60 minutes, centrifugation, by centrifugation gained sediment in 60-90 DEG C, 0.01-
0.05MPa condition is 6-18 hours dry, is then warming up to 900-1100 DEG C with 3-8 DEG C/min of rate, forges at 900-1100 DEG C
Burn 0.5-2 hour, then be warming up to 1200-1500 DEG C with 1-5 DEG C/min of rate, 1200-1500 DEG C calcining 2-4 hours, oneself
The antibacterial agent that D97 partial size is 30-100nm is obtained through air-flow crushing after being so cooled to 25-30 DEG C.The centrifugation is with 5000-
10000 revs/min of revolving speeds are centrifuged 20-60 minutes.
Preferably, in other embodiments of the invention, the preparation method of antibacterial agent is as follows：(1) by 1-3 parts of carbonic acid
Calcium, 1.5-3.5 part zinc oxide, 2-6 parts of boron oxides, 5-10 parts of silica whites, 8-12 parts of aluminium oxide, 28-32 parts of bauxite mixing, add
Enter in 240-270 parts of water, it is the tetrabutylammonium hydroxide aqueous solution of 25-40%, 0.3-0.9 that 0.1-0.5 parts of mass fractions, which are added,
TritonX-100,10-20 parts of ethyl alcohol of part are that 300-800 revs/min of condition stirs 20-60 minutes in 25-35 DEG C, revolving speed,
Ultrasonic frequency is 20-60kHz, power is 300-800W condition ultrasound 20-60 minutes, centrifugation, and centrifugation gained sediment is existed
60-90 DEG C, the drying of 0.01-0.05MPa condition 6-18 hours, are then warming up to 900-1100 DEG C with 3-8 DEG C/min of rate,
900-1100 DEG C calcining 0.5-2 hours, then with 1-5 DEG C/min of rate 1200-1500 DEG C is warming up to, at 1200-1500 DEG C
Calcining 2-4 hours obtains the powder that D97 partial size is 30-100nm through air-flow crushing after naturally cooling to 25-30 DEG C；The centrifugation
It is to be centrifuged 20-60 minutes with 5000-10000 revs/min of revolving speed；(2) by powder be added to quality be 80-120 times of powder quality,
Concentration is in the silver nitrate aqueous solution of 0.005-0.02mol/L, is 100-300 revs/min of condition stirring in 25-35 DEG C, revolving speed
20-60 minutes, it is molten that the ammonium hydroxide that concentration is 0.02-0.1mol/L, quality is 0.002-0.006 times of silver nitrate aqueous solution quality is added
Liquid is that 400-700 revs/min of condition stirs 18-36 hours in 40-50 DEG C, revolving speed, with 5000-10000 revs/min of revolving speed from
The heart 20-60 minutes, centrifugal sediment is taken, it is 18-36 hours dry at 40-65 DEG C, obtain antibacterial agent.Carrier used in embodiment
(i.e. the powder of step (1) preparation) is a kind of porous material, and silver antibacterial agent is fixed on by physical absorption or ion-exchange process
In powder surface or duct, by the sustained release of antibacterial agent effective component to improve antimicrobial long-acting.
The bonding agent is guar gum, one in modified guar gum, starch, modified starch, sodium carboxymethylcellulose
Kind or a variety of mixtures, it is further preferred that the bonding agent is guar gum, modified guar gum, starch, modified shallow lake
One or more mixture in powder.In some embodiments of the invention, bonding agent is the mixing of guar gum and starch
The mass ratio of object, the guar gum and starch is (1-2):(1-2).In some embodiments of the invention, bonding agent is
The mass ratio of the mixture of modified guar gum and starch, the modified guar gum and starch is (1-2):(1-2).In this hair
In bright some embodiments, bonding agent is the mixture of guar gum and modified starch, the guar gum and modified starch
Mass ratio be (1-2):(1-2).Most preferably, bonding agent is the mixture of modified guar gum and modified starch, described
The mass ratio of modified guar gum and modified starch is (1-2):(1-2).The preparation method of modified guar gum is as follows：In nitrogen
Under atmosphere protection, 45-65g water is heated to 70-90 DEG C, 150-200g guar gum is added, in 70-90 DEG C, revolving speed 200-
500 revs/min of conditions stir 30-60 minutes, and 30-50g propyltrichlorosilan, 0.3-1.0g diglycolamine, 15-25g is added and combs
Tooth wormwood artemisia powder, 1-3g polyacrylamide, are warming up to 210-230 DEG C, are that 200-400 revs/min of condition is stirred in 210-230 DEG C, revolving speed
It mixes 2-6 hours, adjusts pH value to 6.8-7.2, be cooled to 25-35 DEG C, obtain modified guar gum.The preparation method of modified starch
It is as follows：10-30g soybean protein isolate, the trimethylamine aqueous solution that 3-6g mass fraction is 25-35% are added to 700-1000g
In water, it is warming up to 85-95 DEG C, is that 100-300 revs/min of condition stirs 40-120 minutes in 85-95 DEG C, revolving speed, is cooled to 55-
65 DEG C, 0.3-0.9g ammonium persulfate is added, is that 100-300 revs/min of condition stirs 10-40 minutes in 55-65 DEG C, revolving speed, adds
Enter 60-90g starch, be warming up to 75-85 DEG C, is that 100-300 revs/min of condition stirs 30-60 minutes in 75-85 DEG C, revolving speed, adds
Enter 1-3g rosin acid, is that 100-300 revs/min of condition stirs 30-60 minutes in 75-85 DEG C, revolving speed, is cooled to 25-35 DEG C, obtains
To modified starch.The silver antibacterial agent of load, which can firmly be adsorbed on web surface, can just play antibacterial effect.Bonding agent makes to resist
Microbial inoculum is preferably immobilized on fiber surface, even across multiple washing, is also able to maintain good antibacterial effect.
The technical effects of the invention are that：
The medical antibacterial quilt cover for facilitating filling of the invention, fabric is soft, and elasticity is good, and filling is easy, and unpicks and washes simple, fabric
Middle addition antimicrobial component, antibiotic property is lasting, and antibacterial range is wide, non-stimulated to skin.Still have after after washing several times good anti-
Bacterium effect, anti-fluffing and anti-pilling effect are good.It is used particularly suitable for the environment of hospital or other bacteriums easy to breed, household etc..This
The medical antibacterial quilt cover for facilitating filling of invention also has far-infrared health-care effect, can enhance human immunity, cytothesis
Ability improves blood microcirculation, boosts metabolism.
Specific embodiment
The present invention is further illustrated below by the mode of embodiment, but does not therefore limit the present invention to the reality
It applies among a range.In the following examples, the experimental methods for specific conditions are not specified, according to conventional methods and conditions, or according to quotient
The selection of product specification.
Embodiment 1
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 85 parts of water.The preparation method of antibiotic finishing solution is：Weigh each raw material by weight, 30 DEG C,
Revolving speed is that 350 revs/min of conditions stir 2 hours, obtains antibiotic finishing solution.
The preparation method of antibacterial agent is as follows：By 1.5 parts of calcium carbonate, 2 parts of zinc oxide, 4 parts of boron oxides, 7 parts of silica whites, 10 parts
Aluminium oxide, 30 parts of bauxite mixing, are added in 250 parts of water, the tetrabutylammonium hydroxide water that 0.3 part of mass fraction is 40% are added
Solution, 0.5 part of TritonX-100,15 parts of ethyl alcohol are that 500 revs/min of conditions stir 40 minutes in 30 DEG C, revolving speed, in ultrasonic wave
Frequency is 40kHz, power is 500W condition ultrasound 25 minutes, is centrifuged 30 minutes with 8000 revs/min of revolving speeds, and centrifugation gained is heavy
Starch was then warming up to 1000 DEG C with 5 DEG C/min of rate, forges at 1000 DEG C in 80 DEG C, the drying of 0.02MPa condition 12 hours
It burns 1 hour, then is warming up to 1300 DEG C with 3 DEG C/min of rate, calcine 3 hours, naturally cooled to after 30 DEG C through gas at 1300 DEG C
Stream, which crushes, obtains the antibacterial agent that D97 partial size is 50nm.
Embodiment 2
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 85 parts of water.The preparation method of antibiotic finishing solution is：Weigh each raw material by weight, 30 DEG C,
Revolving speed is that 350 revs/min of conditions stir 2 hours, obtains antibiotic finishing solution.
The preparation method of antibacterial agent is as follows：(1) by 1.5 parts of calcium carbonate, 2 parts of zinc oxide, 4 parts of boron oxides, 7 parts of silica whites,
10 parts of aluminium oxide, 30 parts of bauxite mixing, are added in 250 parts of water, the tetrabutylammonium hydroxide that 0.3 part of mass fraction is 40% are added
Aqueous ammonium, 0.5 part of TritonX-100,15 parts of ethyl alcohol are that 500 revs/min of conditions stir 40 minutes in 30 DEG C, revolving speed, super
Frequency of sound wave is 40kHz, power is 500W condition ultrasound 25 minutes, is centrifuged 30 minutes with 8000 revs/min of revolving speeds, by being centrifuged
Sediment is obtained in 80 DEG C, the drying of 0.02MPa condition 12 hours, then 1000 DEG C are warming up to 5 DEG C/min of rate, 1000
DEG C calcining 1 hour, then 1300 DEG C is warming up to 3 DEG C/min of rate, is calcined 3 hours at 1300 DEG C, after naturally cooling to 30 DEG C
The powder that D97 partial size is 50nm is obtained through air-flow crushing；(2) powder is added to quality is 100 times of powder quality, concentration is
It is that 150 revs/min of conditions stir 30 minutes in 30 DEG C, revolving speed, concentration, which is added, is in the silver nitrate aqueous solution of 0.01mol/L
0.05mol/L, the ammonia spirit that quality is 0.004 times of silver nitrate aqueous solution quality are 600 revs/min of conditions in 45 DEG C, revolving speed
Stirring 24 hours is centrifuged 25 minutes with 8000 revs/min of revolving speeds, takes centrifugal sediment, 24 hours dry at 50 DEG C, obtains antibacterial
Agent.
Comparative example 1
Substantially the same manner as Example 2, difference is only that, in this comparative example 1：
The preparation method of antibacterial agent is as follows：(1) by 1.5 parts of calcium carbonate, 2 parts of zinc oxide, 4 parts of boron oxides, 7 parts of silica whites,
10 parts of aluminium oxide, 30 parts of bauxite mixing, cross 200 meshes after flour mill is milled and obtain powder, powder is calcined, specifically
Step is：1000 DEG C are warming up to 5 DEG C/min of rate, is calcined 1 hour at 1000 DEG C, then is heated up with 3 DEG C/min of rate
It to 1300 DEG C, is calcined 3 hours at 1300 DEG C, obtains the powder that D97 partial size is 50nm through air-flow crushing after naturally cooling to 30 DEG C；
(2) powder is added to quality is 100 times of powder quality, concentration is in the silver nitrate aqueous solution of 0.01mol/L, in 30 DEG C, turns
Speed stirs 30 minutes for 150 revs/min of conditions, and addition concentration is 0.05mol/L, quality is silver nitrate aqueous solution quality 0.004
Ammonia spirit again is that 600 revs/min of conditions stir 24 hours in 45 DEG C, revolving speed, is centrifuged 25 points with 8000 revs/min of revolving speeds
Clock takes centrifugal sediment, 24 hours dry at 50 DEG C, obtains antibacterial agent.
Embodiment 3
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 4 parts of bonding agent, 85 parts of water.The preparation method of antibacterial agent is same as Example 2.Bonding agent
For the mixture of guar gum and starch, the mass ratio of the guar gum and starch is 1:1.The preparation method of antibiotic finishing solution
For：Each raw material is weighed by weight, is that 350 revs/min of conditions stir 2 hours in 30 DEG C, revolving speed, is obtained antibiotic finishing solution.
Embodiment 4
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 4 parts of bonding agent, 85 parts of water.The preparation method of antibacterial agent is same as Example 2.Bonding agent
For the mixture of modified guar gum and starch, the mass ratio of the modified guar gum and starch is 1:1.Modified guar gum
Preparation method it is as follows：Under nitrogen atmosphere protection, 55g water is heated to 80 DEG C, 175g guar gum is added, in 80 DEG C, turns
Speed stirs 40 minutes for 300 revs/min of conditions, be added 40g propyltrichlorosilan, 0.5g diglycolamine, 20g Pectinate Neopallasia herb powder,
1.5g polyacrylamide is warming up to 220 DEG C, is that 300 revs/min of conditions stir 5 hours in 220 DEG C, revolving speed, adjusting pH value to 7,
30 DEG C are cooled to, modified guar gum is obtained.The preparation method of antibiotic finishing solution is：Weigh each raw material by weight, 30 DEG C,
Revolving speed is that 350 revs/min of conditions stir 2 hours, obtains antibiotic finishing solution.
Embodiment 5
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 4 parts of bonding agent, 85 parts of water.The preparation method of antibacterial agent is same as Example 2.Bonding agent
For the mixture of guar gum and modified starch, the mass ratio of the guar gum and modified starch is 1:1.The system of modified starch
Preparation Method is as follows：25g soybean protein isolate, the trimethylamine aqueous solution that 4g mass fraction is 30% are added in 800g water, risen
Temperature stirs 60 minutes for 200 revs/min of conditions in 90 DEG C, revolving speed to 90 DEG C, is cooled to 60 DEG C, 0.5g ammonium persulfate is added,
60 DEG C, revolving speed be that 200 revs/min of conditions stir 15 minutes, 75g starch is added, 80 DEG C are warming up to, in 80 DEG C, revolving speed 200
Rev/min condition stirs 40 minutes, and 1.5g rosin acid is added, and is that 200 revs/min of conditions stir 40 minutes in 80 DEG C, revolving speed, cold
But to 30 DEG C, modified starch is obtained.The preparation method of antibiotic finishing solution is：Each raw material is weighed by weight, is in 30 DEG C, revolving speed
350 revs/min of conditions stir 2 hours, obtain antibiotic finishing solution.
Embodiment 6
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 4 parts of bonding agent, 85 parts of water.The preparation method of antibacterial agent is same as Example 2.Bonding agent
Only modified guar gum, the preparation method of modified guar gum are same as Example 4.The preparation method of antibiotic finishing solution
For：Each raw material is weighed by weight, is that 350 revs/min of conditions stir 2 hours in 30 DEG C, revolving speed, is obtained antibiotic finishing solution.
Embodiment 7
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 4 parts of bonding agent, 85 parts of water.The preparation method of antibacterial agent is same as Example 2.The bonding
Auxiliary agent is only modified starch, and the preparation method of modified starch is same as Example 5.The preparation method of antibiotic finishing solution is：It presses
Parts by weight weigh each raw material, are that 350 revs/min of conditions stir 2 hours in 30 DEG C, revolving speed, obtain antibiotic finishing solution.
Embodiment 8
A kind of medical antibacterial quilt cover facilitating filling, fabric are antibacterial flexible fabric.Antibacterial flexible fabric is through conventional quilt cover
Processing technology cuts out, sews the medical antibacterial quilt cover for obtaining facilitating filling.
The preparation method of the antibacterial flexible fabric is as follows：By fabric, (100% cotton face fabric is purchased from upper Hydron outstanding person textile
Co., Ltd, grammes per square metre 220g/m2, article No. CJ170-60603) and it immerses in antibiotic finishing solution, bath raio 1:7, dipping temperature 40
DEG C, dip time is 40 minutes, takes out fabric, mangle, pick-up 60% is 6 hours dry at 75 DEG C, 8 points dry at 120 DEG C
Clock obtains antibacterial flexible fabric.
The antibiotic finishing solution includes following components in parts by weight：30 parts of antibacterial agent, 1 part of vinyl front three oxosilane, rouge
0.8 part of fat alcohol polyoxyethylene ether, 4 parts of bonding agent, 85 parts of water.The preparation method of antibacterial agent is same as Example 2.Bonding agent
For the mixture of modified guar gum and modified starch, the mass ratio of the modified guar gum and modified starch is 1:1.It is modified
The preparation method of guar gum is same as Example 4.The preparation method of modified starch is same as Example 5.Antibiotic finishing solution
Preparation method is：Each raw material is weighed by weight, is that 350 revs/min of conditions stir 2 hours in 30 DEG C, revolving speed, it is whole to obtain antibacterial
Manage liquid.
Primary raw material and instrument used are as follows in embodiment：
Fatty alcohol polyoxyethylene ether is AEO-9, Yangtze petrochemical industry-BASF Co., Ltd.Pectinate Neopallasia herb powder：By dry
Pectinate Neopallasia herb (Classification system Neopallasia petinata (Pall.) Poljak) ground complete stool crushes to obtain.It combs in embodiment
The preparation method of tooth wormwood artemisia powder is as follows：It is 15wt% that Pectinate Neopallasia herb, which is dried at 45 DEG C to water content, and crushing sieves with 100 mesh sieve to obtain comb tooth
Wormwood artemisia powder.Calcium carbonate：Powdered whiting, partial size are 1250 mesh.Zinc oxide：Partial size is 325 mesh.Boron oxide：Shanghai Aladdin is biochemical
Science and Technology Co., Ltd., product number B108406.Silica white, Qingdao Marine Chemical Co., Ltd., I class of model, ZCX- I
Type.Aluminium oxide：Partial size is 325 mesh.Bauxite composition is as follows：SiO2：12.10%, TiO2：4.16%, Al2O3：78.08%,
Fe2O3：1.05%, MgO：0.3%, CaO：0.24%, K2O：1.02%, Na2O：0.11%, surplus is impurity.Lingshou County power reaches
Mineral products processing factory provides.40% tetrabutylammonium hydroxide aqueous solution, Shanghai Aladdin biochemical technology limited liability company produce
Product code T 105047.TritonX-100, No. CAS：9002-93-1, Shanghai Aladdin biochemical technology limited liability company, product
Code T 109026.Ethyl alcohol, CAS 64-17-5.Guar gum, No. CAS：9000-30-0, it is limited that Beijing Guar moistens scientific and technological share
Company, model GUARAN-6.Starch, the edible corn starch of Yu Feng Industry Group Co., Ltd production, credit rating level-one are held
Rower is quasi-：GB/T8885-2008.Polyacrylamide, Qingdao tide star reach clearly environmental protection and energy saving Science and Technology Ltd. model QD-522
Anionic polyacrylamide.Soybean protein isolate, from Shaanxi Sen Fu natural product Co., Ltd, model SF702.Flour mill,
HGM90 super fine flour mill, Zhengzhou Dehong mechanical equipment Co., Ltd.
Test case
The antibacterial flexible fabric of the medical antibacterial quilt cover for facilitating filling of the invention is subjected to following test.
Durability of antimicrobial effect can be tested：Using standard GB/T/T 20944.3-2008《The evaluation of antibacterial textile performance
3 parts：Succusion》Antibiotic property quantitative test is carried out, using color fastness to washing testing machine washing methods, after test is washed 300 times
Anti-microbial property, with staphylococcus aureus ATCC No.6538 (gram-positive bacteria) be test strain.
The test of anti-fluffing and anti-pilling performance：According to GB/T4802-1-2008《The measurement of textile fabric pilling performance
1 part：Circular test method》, tested, pressure 590cN, fluffed number 150 times, pilling number 150 times using Circular test method.
The test of far infrared normal emittance：It is soft to antibacterial according to far infrared textile inspection standard Fz/T64010-2000
Property fabric carry out normal emittance detection.
Table 1：Bacteriostasis rate and far infrared normal emittance test result table
| Bacteriostasis rate/% | Normal emittance/% | |
| Embodiment 1 | 50.4 | 82.4 |
| Embodiment 2 | 82.5 | 82.7 |
| Comparative example 1 | 77.9 | 78.6 |
| Embodiment 3 | 83.5 | 86.6 |
| Embodiment 4 | 88.2 | 91.5 |
| Embodiment 5 | 87.1 | 90.0 |
| Embodiment 6 | 92.5 | 92.2 |
| Embodiment 7 | 90.6 | 91.3 |
| Embodiment 8 | 97.4 | 95.5 |
Table 2：Anti-fluffing and anti-pilling performance test result table
| Anti-fluffing and anti-pilling grade | |
| Embodiment 3 | 3 grades |
| Embodiment 6 | 4 grades |
| Embodiment 7 | 4 grades |
| Embodiment 8 | 5 grades |
The medical antibacterial quilt cover for facilitating filling of the invention, fabric is soft, and elasticity is good, and filling is easy, and unpicks and washes simple, fabric
Middle addition antimicrobial component, antibiotic property is lasting, and antibacterial range is wide, non-stimulated to skin.Still have after after washing several times good anti-
Bacterium effect, anti-fluffing and anti-pilling effect are good.It is used particularly suitable for the environment of hospital or other bacteriums easy to breed, household etc..This
The medical antibacterial quilt cover for facilitating filling of invention also has far-infrared health-care effect, can enhance human immunity, cytothesis
Ability improves blood microcirculation, boosts metabolism.
The preferred embodiment of the present invention has been described in detail above.It should be appreciated that those skilled in the art without
It needs creative work according to the present invention can conceive and makes many modifications and variations.Therefore, all technologies in the art
Personnel are available by logical analysis, reasoning, or a limited experiment on the basis of existing technology under this invention's idea
Technical solution, all should be within the scope of protection determined by the claims.
Claims (10)
1. a kind of medical antibacterial quilt cover for facilitating filling, which is characterized in that fabric is antibacterial flexible fabric.
2. the medical antibacterial quilt cover according to claim 1 for facilitating filling, which is characterized in that the antibacterial flexible fabric
Preparation method is as follows：Fabric is immersed in antibiotic finishing solution, bath raio 1:(5-10), dipping temperature are 35-45 DEG C, dip time
It is 30-60 minutes, takes out fabric, mangle, pick-up 40%-70% is 5-10 hours dry at 65-80 DEG C, at 115-125 DEG C
It is 5-10 minutes dry, obtain antibacterial flexible fabric.
3. the medical antibacterial quilt cover according to claim 2 for facilitating filling, which is characterized in that the antibiotic finishing solution includes
Following components in parts by weight：25-35 parts of antibacterial agent, 0.5-1.5 parts of vinyl front three oxosilane, fatty alcohol polyoxyethylene ether 0.5-
1.5 parts, 80-100 parts of water.
4. the medical antibacterial quilt cover according to claim 3 for facilitating filling, which is characterized in that the antibiotic finishing solution includes
Following components in parts by weight：25-35 parts of antibacterial agent, 0.5-1.5 parts of vinyl front three oxosilane, fatty alcohol polyoxyethylene ether 0.5-
1.5 parts, 3-5 parts of bonding agent, 80-100 parts of water.
5. the medical antibacterial quilt cover according to claim 3 or 4 for facilitating filling, which is characterized in that the system of the antibacterial agent
Preparation Method is as follows：By 1-3 parts of calcium carbonate, 1.5-3.5 parts of zinc oxide, 2-6 parts of boron oxides, 5-10 parts of silica whites, 8-12 parts of oxidations
Aluminium, 28-32 parts of bauxite mixing, are added in 240-270 parts of water, and the tetrabutyl that 0.1-0.5 parts of mass fractions are 25-40% is added
Ammonium hydroxide aqueous solution, 0.3-0.9 part TritonX-100,10-20 part ethyl alcohol are 300-800 revs/min in 25-35 DEG C, revolving speed
Clock condition stirs 20-60 minutes, ultrasonic frequency is 20-60kHz, power is 300-800W condition ultrasound 20-60 minutes, from
The heart, by centrifugation gained sediment in 60-90 DEG C, the drying of 0.01-0.05MPa condition 6-18 hours, then with 3-8 DEG C/min
Rate is warming up to 900-1100 DEG C, 900-1100 DEG C calcining 0.5-2 hours, then be warming up to 1-5 DEG C/min of rate
1200-1500 DEG C, 1200-1500 DEG C calcining 2-4 hours, obtain D97 partial size through air-flow crushing after naturally cooling to 25-30 DEG C
For the antibacterial agent of 30-100nm.
6. the medical antibacterial quilt cover according to claim 3 or 4 for facilitating filling, which is characterized in that the system of the antibacterial agent
Preparation Method is as follows：(1) by 1-3 parts of calcium carbonate, 1.5-3.5 parts of zinc oxide, 2-6 parts of boron oxides, 5-10 parts of silica whites, 8-12 parts of oxygen
Change aluminium, 28-32 parts of bauxite mixing, is added in 240-270 parts of water, four fourths that 0.1-0.5 parts of mass fractions are 25-40% are added
Base ammonium hydroxide aqueous solution, 0.3-0.9 part TritonX-100,10-20 part ethyl alcohol, 25-35 DEG C, revolving speed be 300-800 turn/
Minute condition stirs 20-60 minutes, ultrasonic frequency is 20-60kHz, power is 300-800W condition ultrasound 20-60 minutes,
Centrifugation, by centrifugation gained sediment in 60-90 DEG C, the drying of 0.01-0.05MPa condition 6-18 hours, then with 3-8 DEG C/min
Rate be warming up to 900-1100 DEG C, 900-1100 DEG C calcining 0.5-2 hours, then be warming up to 1-5 DEG C/min of rate
1200-1500 DEG C, 1200-1500 DEG C calcining 2-4 hours, obtain D97 partial size through air-flow crushing after naturally cooling to 25-30 DEG C
For the powder of 30-100nm；(2) powder is added to quality is 80-120 times of powder quality, concentration 0.005-0.02mol/L
Silver nitrate aqueous solution in, be that 100-300 revs/min of condition stirs 20-60 minute in 25-35 DEG C, revolving speed, addition concentration is
0.02-0.1mol/L, the ammonia spirit that quality is 0.002-0.006 times of silver nitrate aqueous solution quality are in 40-50 DEG C, revolving speed
400-700 revs/min of condition stirs 18-36 hours, is centrifuged 20-60 minutes with 5000-10000 revs/min of revolving speed, takes centrifugation heavy
Starch, it is 18-36 hours dry at 40-65 DEG C, obtain antibacterial agent.
7. the medical antibacterial quilt cover according to claim 4 for facilitating filling, which is characterized in that the bonding agent is Guar
Bean gum, modified guar gum, starch, modified starch, mixture one or more in sodium carboxymethylcellulose.
8. the medical antibacterial quilt cover according to claim 7 for facilitating filling, which is characterized in that the bonding agent is Guar
Bean gum, modified guar gum, starch, mixture one or more in modified starch.
9. the medical antibacterial quilt cover according to claim 7 or 8 for facilitating filling, which is characterized in that modified guar gum
Preparation method is as follows：Under nitrogen atmosphere protection, 45-65g water is heated to 70-90 DEG C, 150-200g guar gum is added,
70-90 DEG C, revolving speed be that 200-500 revs/min of condition stirs 30-60 minute, addition 30-50g propyltrichlorosilan, 0.3-1.0g
Diglycolamine, 15-25g Pectinate Neopallasia herb powder, 1-3g polyacrylamide, are warming up to 210-230 DEG C, in 210-230 DEG C, revolving speed 200-
400 revs/min of conditions stir 2-6 hours, adjust pH value to 6.8-7.2, are cooled to 25-35 DEG C, obtain modified guar gum.
10. the medical antibacterial quilt cover according to claim 7 or 8 for facilitating filling, which is characterized in that the modified starch
Preparation method is as follows：10-30g soybean protein isolate, the trimethylamine aqueous solution that 3-6g mass fraction is 25-35% are added to
In 700-1000g water, it is warming up to 85-95 DEG C, is that 100-300 revs/min of condition stirs 40-120 minutes in 85-95 DEG C, revolving speed,
It is cooled to 55-65 DEG C, 0.3-0.9g ammonium persulfate is added, is that 100-300 revs/min of condition stirs 10- in 55-65 DEG C, revolving speed
40 minutes, 60-90g starch is added, is warming up to 75-85 DEG C, is that 100-300 revs/min of condition stirs 30- in 75-85 DEG C, revolving speed
60 minutes, 1-3g rosin acid is added, is that 100-300 revs/min of condition stirs 30-60 minutes in 75-85 DEG C, revolving speed, is cooled to
25-35 DEG C, obtain modified starch.
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| CN109667144A (en) * | 2018-12-15 | 2019-04-23 | 南通开发区翔华纺织品织造有限公司 | A kind of antibacterial quilt cover and its production technology |
| CN109662519A (en) * | 2019-01-29 | 2019-04-23 | 刘群英 | A kind of combined bed mattress |
| CN109881477A (en) * | 2019-02-20 | 2019-06-14 | 常州海瑞纺织品有限公司 | A kind of antimicrobial form fabric and preparation method thereof |
| CN112323496A (en) * | 2020-11-13 | 2021-02-05 | 苏州斯诺服饰有限公司 | Preparation method of antibacterial fabric, fabric prepared by using preparation method and windproof clothes |
| CN113417142A (en) * | 2021-06-22 | 2021-09-21 | 杭州萧山凤凰纺织有限公司 | Antibacterial non-woven fabric and preparation method thereof |
| CN113463380A (en) * | 2021-07-26 | 2021-10-01 | 河南迪怡疗护科技开发有限公司 | Antibacterial fabric and production method thereof |
| CN113652861A (en) * | 2021-08-31 | 2021-11-16 | 河南迪怡疗护科技开发有限公司 | Fabric with antibacterial and antistatic functions |
| CN116065384A (en) * | 2023-01-17 | 2023-05-05 | 上海洁宜康化工科技有限公司 | Silver-containing antibacterial liquid composition, preparation method and application thereof |
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| CN113652861A (en) * | 2021-08-31 | 2021-11-16 | 河南迪怡疗护科技开发有限公司 | Fabric with antibacterial and antistatic functions |
| CN116065384A (en) * | 2023-01-17 | 2023-05-05 | 上海洁宜康化工科技有限公司 | Silver-containing antibacterial liquid composition, preparation method and application thereof |
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