CN112342691B - Elastic antibacterial non-woven fabric and manufacturing process thereof - Google Patents
Elastic antibacterial non-woven fabric and manufacturing process thereof Download PDFInfo
- Publication number
- CN112342691B CN112342691B CN202011204764.4A CN202011204764A CN112342691B CN 112342691 B CN112342691 B CN 112342691B CN 202011204764 A CN202011204764 A CN 202011204764A CN 112342691 B CN112342691 B CN 112342691B
- Authority
- CN
- China
- Prior art keywords
- parts
- exchange resin
- ion exchange
- core layer
- woven 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.)
- Active
Links
- 239000004745 nonwoven fabric Substances 0.000 title claims abstract description 72
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 53
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 25
- -1 polyethylene terephthalate Polymers 0.000 claims abstract description 88
- 239000012792 core layer Substances 0.000 claims abstract description 72
- 239000010410 layer Substances 0.000 claims abstract description 68
- 239000000835 fiber Substances 0.000 claims abstract description 63
- 239000002131 composite material Substances 0.000 claims abstract description 52
- 239000002994 raw material Substances 0.000 claims abstract description 47
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 37
- 239000000945 filler Substances 0.000 claims abstract description 36
- 239000000839 emulsion Substances 0.000 claims abstract description 35
- 229920000139 polyethylene terephthalate Polymers 0.000 claims abstract description 27
- 239000005020 polyethylene terephthalate Substances 0.000 claims abstract description 27
- NAEDWKNFXVUORY-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;hexanedioic acid Chemical compound OCC(CO)(CO)CO.OC(=O)CCCCC(O)=O NAEDWKNFXVUORY-UHFFFAOYSA-N 0.000 claims abstract description 16
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 81
- 239000003456 ion exchange resin Substances 0.000 claims description 81
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 81
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 66
- VYNIYUVRASGDDE-UHFFFAOYSA-N silver zirconium Chemical compound [Zr].[Ag] VYNIYUVRASGDDE-UHFFFAOYSA-N 0.000 claims description 50
- 238000001035 drying Methods 0.000 claims description 32
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 26
- 238000010438 heat treatment Methods 0.000 claims description 25
- 229920001577 copolymer Polymers 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 229920003225 polyurethane elastomer Polymers 0.000 claims description 18
- 238000005303 weighing Methods 0.000 claims description 18
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 17
- 229920000570 polyether Polymers 0.000 claims description 17
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 16
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 16
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 16
- 229910017604 nitric acid Inorganic materials 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
- 239000008367 deionised water Substances 0.000 claims description 14
- 229910021641 deionized water Inorganic materials 0.000 claims description 14
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 12
- 238000009960 carding Methods 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 12
- 238000000967 suction filtration Methods 0.000 claims description 12
- WSFMFXQNYPNYGG-UHFFFAOYSA-M dimethyl-octadecyl-(3-trimethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC)(OC)OC WSFMFXQNYPNYGG-UHFFFAOYSA-M 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 11
- UJVRJBAUJYZFIX-UHFFFAOYSA-N nitric acid;oxozirconium Chemical compound [Zr]=O.O[N+]([O-])=O.O[N+]([O-])=O UJVRJBAUJYZFIX-UHFFFAOYSA-N 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 8
- 230000003014 reinforcing effect Effects 0.000 claims description 8
- 239000004332 silver Substances 0.000 claims description 8
- 229910052709 silver Inorganic materials 0.000 claims description 8
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 8
- 229910052726 zirconium Inorganic materials 0.000 claims description 8
- 230000002787 reinforcement Effects 0.000 claims description 7
- 238000002791 soaking Methods 0.000 claims description 7
- 235000019270 ammonium chloride Nutrition 0.000 claims description 6
- 239000003957 anion exchange resin Substances 0.000 claims description 6
- 238000007664 blowing Methods 0.000 claims description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 6
- 238000009826 distribution Methods 0.000 claims description 6
- 238000011068 loading method Methods 0.000 claims description 6
- 230000007935 neutral effect Effects 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 238000009987 spinning Methods 0.000 claims description 6
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical compound CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 claims description 6
- 238000001291 vacuum drying Methods 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 238000004804 winding Methods 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims description 4
- 239000004744 fabric Substances 0.000 abstract description 7
- 101710134784 Agnoprotein Proteins 0.000 description 7
- 239000003242 anti bacterial agent Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 239000004750 melt-blown nonwoven Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229920006052 Chinlon® Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
- D04H1/492—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres by fluid jet
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/08—Melt spinning methods
- D01D5/098—Melt spinning methods with simultaneous stretching
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/28—Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
- D01D5/30—Conjugate filaments; Spinnerette packs therefor
- D01D5/34—Core-skin structure; Spinnerette packs therefor
-
- 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
-
- 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
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
-
- 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
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/16—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds as constituent
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/13—Physical properties anti-allergenic or anti-bacterial
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The invention discloses an elastic antibacterial non-woven fabric and a manufacturing process thereof, wherein the elastic antibacterial non-woven fabric is prepared from composite fibers by a spunlace non-woven fabric production process; the composite fiber has a sheath-core structure, including a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: (0.28-0.35); the core layer is prepared from the following raw materials in parts by weight: 95-100 parts of polyethylene terephthalate, 2-5 parts of hydroxyl-terminated polysiloxane emulsion, 2-3.5 parts of pentaerythritol adipate and 10-15 parts of filler. The elastic antibacterial non-woven fabric is excellent in antibacterial performance and good in antibacterial effect; the fracture strength is high, and the mechanical property is good; in addition, the elastic fabric has good elasticity and softness.
Description
The invention relates to a divisional application of an invention patent application with the application number of 201911020807.0, the application date of 2019, 10 and 25 months and the name of 'an antibacterial non-woven fabric and a manufacturing process thereof'.
Technical Field
The invention relates to the technical field of non-woven fabrics, in particular to an elastic antibacterial non-woven fabric and a manufacturing process thereof.
Background
The fiber for producing the non-woven fabric is mainly polypropylene (PP) and Polyester (PET). In addition, there are chinlon (PA), viscose, acrylic, polyethylene (HDPE), polyvinyl chloride (PVC). The non-woven fabric is classified into a disposable type and a durable type according to application requirements.
The production process comprises the following steps:
1. water-jetting non-woven fabric: the spunlace process is to spray high-pressure fine water flow onto one or more layers of fiber webs to enable the fibers to be mutually entangled, so that the fiber webs are reinforced and have certain strength.
2. Heat sealing the non-woven fabric: the thermal bonding non-woven fabric is formed by adding fibrous or powdery hot melt bonding reinforcing materials into a fiber web, and heating, melting, cooling and reinforcing the fiber web into a fabric.
3. Pulp air-laid nonwoven fabric: the air-laid nonwoven fabric can be called as dust-free paper and dry papermaking nonwoven fabric. It adopts the air-laid technology to open the wood pulp fiber board into single fiber state, then uses the air-laid method to make the fiber agglutinate on the net-forming curtain, then the net is consolidated into cloth.
4. Wet non-woven fabric: the wet-process non-woven fabric is made up through opening the raw fibre material in water medium to obtain single fibre, mixing different fibre materials to obtain fibre suspension pulp, delivering the suspension pulp to net-forming mechanism, and wet-forming and solidifying.
5. Spun-bonded nonwoven fabric: spunbond nonwoven fabrics are nonwoven fabrics formed by extruding and drawing a polymer to form continuous filaments, laying the filaments into a web, and then converting the web into a nonwoven fabric by autogenous bonding, thermal bonding, chemical bonding or mechanical consolidation.
6. Melt-blown nonwoven fabric: the process of melt-blown non-woven fabric comprises the following steps: polymer feeding, melt extrusion, fiber formation, fiber cooling, web forming and cloth reinforcement.
7. Needling the non-woven fabric: the needle-punched non-woven fabric is one of dry non-woven fabrics, and the needle-punched non-woven fabric is formed by reinforcing a fluffy fiber web into a fabric by utilizing the piercing effect of a needle.
8. Stitching and knitting non-woven fabrics: stitchbonded nonwovens are one type of dry-laid nonwovens that are made by consolidating webs, layers of yarn, nonwoven materials (e.g., plastic sheets, plastic foils, etc.), or combinations thereof, with a warp-knitted loop structure.
9. Hydrophilic non-woven fabric: is mainly used for the production of medical and health materials to obtain better hand feeling and no scratch to skin. Like sanitary napkins and sanitary pads, the hydrophilic function of hydrophilic nonwoven fabrics is utilized.
However, the antibacterial nonwoven fabric used at present has the following problems:
the antibacterial effect is poor, the mechanical properties such as breaking strength and the like of the prepared antibacterial non-woven fabric are poor due to the fact that a large amount of antibacterial filler is used, and the application range is limited;
the mode of impregnating the surface with the antibacterial agent or adding the small-molecular antibacterial agent is easy to seep out and dissolve in a solvent or water, so that the antibacterial effect is easily and greatly weakened, and even the antibacterial effect is lost.
Disclosure of Invention
Based on the above situation, the present invention aims to provide an elastic antibacterial nonwoven fabric and a manufacturing process thereof, which can effectively solve the above problems.
In order to solve the technical problems, the technical scheme provided by the invention is as follows:
an elastic antibacterial non-woven fabric is prepared by composite fibers through a spunlace non-woven fabric production process;
the composite fiber has a sheath-core structure comprising a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: (0.28-0.35);
the core layer is prepared from the following raw materials in parts by weight: 95-100 parts of polyethylene terephthalate, 2-5 parts of hydroxyl-terminated polysiloxane emulsion (the invention is mainly used for improving the flexibility of products by introducing the hydroxyl-terminated polysiloxane emulsion with a proper proportion, and also can improve the fluidity of a mixture during melt mixing, and simultaneously improve the compatibility of raw materials, and in addition, because of the hydroxyl-terminated polysiloxane emulsion, a small amount of hydroxyl-terminated polysiloxane can react with hexamethylene diisocyanate at high temperature to increase the bonding firmness with a skin layer), 2-3.5 parts of pentaerythritol adipate (the invention is mainly used for plasticizing by introducing the pentaerythritol adipate with a proper proportion and has good compatibility with the polyethylene terephthalate), and 10-15 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 55-65 parts of polyethylene terephthalate, 30-35 parts of polyether polyurethane elastomer, 10-13 parts of maleic anhydride grafted ethylene-octene copolymer (the polyether polyurethane elastomer and the maleic anhydride grafted ethylene-octene copolymer are both elastomers and have good compatibility in a raw material composition system and are mainly used for improving the mechanical property of finally prepared non-woven fabric), 2.5-4.5 parts of hydroxyl-terminated polysiloxane emulsion (the invention introduces the hydroxyl-terminated polysiloxane emulsion with a proper proportion and is mainly used for improving the flexibility of a product, also can improve the fluidity of a mixture during melt mixing and simultaneously improves the compatibility of the raw materials, in addition, as the hydroxyl-terminated polysiloxane emulsion is provided, part of the hydroxyl-terminated polysiloxane can react with hexamethylene diisocyanate at high temperature to generate mild crosslinking), 3-5 parts of hexamethylene diisocyanate and 5-9 parts of silver-zirconium loaded ion exchange resin, 2-4 parts of dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and 8-12 parts of a filler.
Preferably, the ratio of the cross-sectional areas of the core layer and the skin layer is 1: 0.32 of;
the core layer is prepared from the following raw materials in parts by weight: 97.5 parts of polyethylene terephthalate, 3.5 parts of hydroxyl-terminated polysiloxane emulsion, 2.8 parts of pentaerythritol adipate and 12.5 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 60 parts of polyethylene terephthalate, 32.5 parts of polyether polyurethane elastomer, 11.5 parts of maleic anhydride grafted ethylene-octene copolymer, 3.3 parts of hydroxyl-terminated polysiloxane emulsion, 4 parts of hexamethylene diisocyanate, 7.2 parts of silver-zirconium loaded ion exchange resin, 3 parts of dimethyloctadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and 10 parts of filler.
Preferably, the preparation method of the silver-zirconium loaded ion exchange resin comprises the following steps:
s1, preparing a silver-zirconium loading solution:
using silver nitrate (AgNO) 3 ) Zirconium oxynitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentrated nitric acid and deionized water to prepare a silver-zirconium load solution containing 1.15-1.45 mol/L of silver ions, 0.18-0.26 mol/L of zirconium ions and 4-6% of nitric acid concentration;
s2, weighing ion exchange resin, adding the ion exchange resin into a reaction container, adding the silver-zirconium load solution in an amount which is 40-50 times the weight of the ion exchange resin, and stirring for 4-6 hours at room temperature under a 8-10T superconducting strong magnetic field;
s3, stopping stirring, standing for 2-4 h, performing suction filtration, separating the reacted ion exchange resin, and adding the separated ion exchange resin into a sodium hydroxide (NaOH) solution with the mass concentration of 5-7% to soak for 20-30 min;
s4, performing suction filtration, separating the ion exchange resin in the sodium hydroxide (NaOH) solution, washing the ion exchange resin to be neutral by using deionized water, drying, and crushing to 200-500 meshes to obtain the silver-zirconium loaded ion exchange resin.
Preferably, silver nitrate (AgNO) is used in step S1 3 ) Zirconyl nitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentrated nitric acid and deionized water to prepare silver-zirconium load solution containing 1.34mol/L silver ions, 0.22mol/L zirconium ions and 5.5 percent nitric acid.
Preferably, in step S2, the ion exchange resin is a D301 type anion exchange resin.
Preferably, the pH of the solution is maintained above 9 throughout the soaking step S3.
Preferably, in step S4, the drying is performed by vacuum drying, and the drying temperature is controlled to be 50 to 60 ℃.
Preferably, the maleic anhydride grafting ratio of the maleic anhydride grafted ethylene-octene copolymer is 0.9-1.2%.
Preferably, the filler is nano calcium carbonate.
The invention also provides a manufacturing process of the elastic antibacterial non-woven fabric, which comprises the following steps:
A. weighing the raw materials of the core layer according to the parts by weight: polyethylene glycol terephthalate, hydroxyl-terminated polysiloxane emulsion, pentaerythritol adipate and filler are uniformly mixed and dried for later use; weighing the raw materials of the cortex respectively according to the parts by weight: polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer, hydroxyl-terminated polysiloxane emulsion, hexamethylene diisocyanate, ion exchange resin loaded with silver-zirconium, dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and filler, uniformly mixing and drying for later use;
B. feeding the raw materials of the core layer into a double-screw extruder to be melted into a core layer mixed melt; feeding the raw materials of the skin layer into a single screw extruder to be melted into a skin layer mixed melt;
C. the core layer mixed melt and the skin layer mixed melt enter a composite spinning machine, are sprayed out from a composite spinneret plate after being subjected to melt distribution to form a strand silk with a skin-core structure of the core layer and the skin layer, and are subjected to air blowing cooling, stretching and winding to obtain composite fibers; the fineness of the composite fiber is 2-5 dtex;
D. carding the composite fibers into a web, then carrying out spunlace reinforcement and drying to obtain the elastic antibacterial non-woven fabric;
in the step B, the heating section of the double-screw extruder is 6 sections, and the heating temperature is 222-232 ℃, 236-242 ℃, 250-255 ℃, 260-265 ℃, 268-272 ℃ and 272-285 ℃ in sequence; the heating section of the single-screw extruder is 5 sections, and the heating temperature is 222-230 ℃, 236-246 ℃, 253-259 ℃, 265-272 ℃ and 275-280 ℃ in sequence; in the step D, when the mixed fibers are carded into a web, the rotating speed of a main cylinder of the carding machine is 760-820 m/min, the rotating speed of a working roller is 60-68 m/min, and the rotating speed of a stripping roller is 78-86 m/min; 5-9 spunlace heads are adopted for spunlacing and reinforcing the mixed fiber web; the pressure range of the plurality of the water stabs is 40-48 bar.
Compared with the prior art, the invention has the following advantages and beneficial effects:
the elastic antibacterial non-woven fabric is prepared from composite fibers through a spunlace non-woven fabric production process, wherein the composite fibers have a skin-core structure and comprise a core layer and a skin layer, the core layer and the skin layer are respectively selected from raw materials, the content of each raw material is optimized, the advantages of the composite fibers are fully exerted, the composite fibers complement each other and promote each other, and the prepared elastic antibacterial non-woven fabric is excellent in antibacterial performance and good in antibacterial effect; the modified polyurethane elastomer has high breaking strength and good mechanical property, and also has good elasticity (mainly the addition of the polyether polyurethane elastomer and the maleic anhydride grafted ethylene-octene copolymer) and softness (mainly the addition of the hydroxyl-terminated polysiloxane emulsion).
The elastic antibacterial non-woven fabric is added with the silver-zirconium loaded ion exchange resin and the dimethyl octadecyl [3- (trimethoxy silicon) propyl ] ammonium chloride which are used as composite antibacterial agents in a proper proportion, the composite antibacterial agent is matched with other components, the compatibility is good, the composite antibacterial agent is uniformly dispersed in base materials (polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer and the like), the bonding strength is high, and the prepared elastic antibacterial non-woven fabric has excellent antibacterial performance and good antibacterial effect; and the antibacterial agent (component) is not easy to seep out, is not easy to dissolve in a solvent or water, and has a long antibacterial effect.
The elastic antibacterial non-woven fabric ensures that the prepared elastic antibacterial non-woven fabric has excellent antibacterial performance and high breaking strength by controlling the ratio of the cross-sectional areas of the core layer and the skin layer; meanwhile, the addition of the silver-zirconium loaded ion exchange resin and dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride as the composite antibacterial agent is saved, and the cost of raw materials is saved.
The invention has simple manufacturing process and simple and convenient operation, and saves manpower and equipment cost.
Detailed Description
In order that those skilled in the art will better understand the technical solutions of the present invention, the following description will be given with reference to specific examples, but it should not be construed as limiting the present patent.
The test methods or test methods described in the following examples are conventional methods unless otherwise specified; the reagents and materials, unless otherwise specified, are either commercially available from conventional sources or are prepared in conventional manners.
Example 1:
an elastic antibacterial non-woven fabric is prepared by composite fibers through a spunlace non-woven fabric production process;
the composite fiber has a sheath-core structure, including a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: (0.28-0.35);
the core layer is prepared from the following raw materials in parts by weight: 95-100 parts of polyethylene terephthalate, 2-5 parts of hydroxyl-terminated polysiloxane emulsion, 2-3.5 parts of pentaerythritol adipate and 10-15 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 55-65 parts of polyethylene terephthalate, 30-35 parts of polyether polyurethane elastomer, 10-13 parts of maleic anhydride grafted ethylene-octene copolymer, 2.5-4.5 parts of hydroxyl-terminated polysiloxane emulsion, 3-5 parts of hexamethylene diisocyanate, 5-9 parts of silver-zirconium loaded ion exchange resin, 2-4 parts of dimethyl octadecyl [3- (trimethoxy silicon-based) propyl ] ammonium chloride and 8-12 parts of filler.
Preferably, the ratio of the cross-sectional areas of the core layer and the skin layer is 1: 0.32 of;
the core layer is prepared from the following raw materials in parts by weight: 97.5 parts of polyethylene terephthalate, 3.5 parts of hydroxyl-terminated polysiloxane emulsion, 2.8 parts of pentaerythritol adipate and 12.5 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 60 parts of polyethylene terephthalate, 32.5 parts of polyether polyurethane elastomer, 11.5 parts of maleic anhydride grafted ethylene-octene copolymer, 3.3 parts of hydroxyl-terminated polysiloxane emulsion, 4 parts of hexamethylene diisocyanate, 7.2 parts of silver-zirconium loaded ion exchange resin, 3 parts of dimethyloctadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and 10 parts of filler.
Preferably, the preparation method of the silver-zirconium loaded ion exchange resin comprises the following steps:
s1, preparing a silver-zirconium loading solution:
using silver nitrate (AgNO) 3 ) Zirconyl nitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentratedPreparing silver-zirconium load solution containing 1.15-1.45 mol/L silver ions, 0.18-0.26 mol/L zirconium ions and 4-6% nitric acid by using nitric acid and deionized water;
s2, weighing ion exchange resin, adding the ion exchange resin into a reaction container, adding the silver-zirconium load solution in an amount which is 40-50 times the weight of the ion exchange resin, and stirring for 4-6 hours at room temperature under a 8-10T superconducting strong magnetic field;
s3, stopping stirring, standing for 2-4 h, performing suction filtration, separating the reacted ion exchange resin, and adding the separated ion exchange resin into a sodium hydroxide (NaOH) solution with the mass concentration of 5-7% to soak for 20-30 min;
s4, performing suction filtration, separating the ion exchange resin in the sodium hydroxide (NaOH) solution, washing the ion exchange resin to be neutral by using deionized water, drying, and crushing to 200-500 meshes to obtain the silver-zirconium loaded ion exchange resin.
Preferably, in step S1, silver nitrate (AgNO) is used 3 ) Zirconyl nitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentrated nitric acid and deionized water to prepare silver-zirconium load solution containing 1.34mol/L silver ions, 0.22mol/L zirconium ions and 5.5 percent nitric acid.
Preferably, in step S2, the ion exchange resin is a D301 type anion exchange resin.
Preferably, the pH of the solution is maintained above 9 throughout the soaking step S3.
Preferably, in step S4, the drying is performed by vacuum drying, and the drying temperature is controlled to be 50 to 60 ℃.
Preferably, the maleic anhydride grafting ratio of the maleic anhydride grafted ethylene-octene copolymer is 0.9-1.2%.
Preferably, the filler is nano calcium carbonate.
The embodiment also provides a manufacturing process of the elastic antibacterial non-woven fabric, which comprises the following steps:
A. respectively weighing the raw materials of the core layer in parts by weight: polyethylene terephthalate, hydroxyl-terminated polysiloxane emulsion, pentaerythritol adipate and filler, uniformly mixing and drying for later use; weighing the raw materials of the cortex respectively according to the parts by weight: polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer, hydroxyl-terminated polysiloxane emulsion, hexamethylene diisocyanate, silver-zirconium loaded ion exchange resin, dimethyl octadecyl [3- (trimethoxy silicon) propyl ] ammonium chloride and filler, uniformly mixing and drying for later use;
B. feeding the raw materials of the core layer into a double-screw extruder to be melted into a core layer mixed melt; feeding the raw materials of the skin layer into a single screw extruder to be melted into a skin layer mixed melt;
C. the core layer mixed melt and the skin layer mixed melt enter a composite spinning machine, are sprayed out from a composite spinneret plate after being subjected to melt distribution to form strand silk with a skin-core structure of the core layer and the skin layer, and are subjected to air blowing cooling, stretching and winding to obtain composite fibers; the fineness of the composite fiber is 2-5 dtex;
D. carding the composite fibers into a web, then carrying out spunlace reinforcement, and drying to obtain the elastic antibacterial non-woven fabric;
in the step B, the heating section of the double-screw extruder is 6 sections, and the heating temperature is 222-232 ℃, 236-242 ℃, 250-255 ℃, 260-265 ℃, 268-272 ℃ and 272-285 ℃ in sequence; the heating section of the single-screw extruder is 5 sections, and the heating temperature is 222-230 ℃, 236-246 ℃, 253-259 ℃, 265-272 ℃ and 275-280 ℃ in sequence; in the step D, when the mixed fibers are carded into a net, the rotating speed of a main cylinder of the carding machine is 760-820 m/min, the rotating speed of a working roller is 60-68 m/min, and the rotating speed of a stripping roller is 78-86 m/min; the number of the spunlace heads used for spunlacing and reinforcing the mixed fiber web is 5-9; the pressure range of the plurality of the water stabs is 40-48 bar.
Example 2:
an elastic antibacterial non-woven fabric is prepared by composite fibers through a spunlace non-woven fabric production process;
the composite fiber has a sheath-core structure comprising a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: 0.28;
the core layer is prepared from the following raw materials in parts by weight: 95 parts of polyethylene terephthalate, 2 parts of hydroxyl-terminated polysiloxane emulsion, 2 parts of pentaerythritol adipate and 10 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 55 parts of polyethylene terephthalate, 30 parts of polyether polyurethane elastomer, 10 parts of maleic anhydride grafted ethylene-octene copolymer, 2.5 parts of hydroxyl-terminated polysiloxane emulsion, 3 parts of hexamethylene diisocyanate, 5 parts of silver-zirconium loaded ion exchange resin, 2 parts of dimethyloctadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and 8 parts of filler.
In this embodiment, the preparation method of the silver-zirconium loaded ion exchange resin comprises the following steps:
s1, preparing a silver-zirconium loading solution:
using silver nitrate (AgNO) 3 ) Zirconyl nitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentrated nitric acid and deionized water to prepare silver-zirconium load solution containing 1.15mol/L silver ions, 0.18mol/L zirconium ions and 4 percent nitric acid;
s2, weighing ion exchange resin, adding the ion exchange resin into a reaction container, adding the silver-zirconium load solution which is 40 times of the ion exchange resin in weight, and stirring for 4 hours at room temperature under a 8T superconducting strong magnetic field;
s3, stopping stirring, standing for 2 hours, performing suction filtration, separating the reacted ion exchange resin, and adding the separated ion exchange resin into a sodium hydroxide (NaOH) solution with the mass concentration of 5% to soak for 30 min;
s4, carrying out suction filtration, separating out the ion exchange resin in the sodium hydroxide (NaOH) solution, washing the ion exchange resin to be neutral by using deionized water, drying, and crushing to 200 meshes to obtain the silver-zirconium loaded ion exchange resin.
In this embodiment, in step S2, the ion exchange resin is a D301 type anion exchange resin.
In this example, the pH of the solution was maintained above 9 throughout the soaking process in step S3.
In this embodiment, in step S4, the drying is performed by vacuum drying, and the drying temperature is controlled at 50 ℃.
In this example, the maleic anhydride-grafted ethylene-octene copolymer had a maleic anhydride grafting ratio of 0.9%.
In this embodiment, the filler is nano calcium carbonate.
In this embodiment, the process for manufacturing the elastic antibacterial non-woven fabric includes the following steps:
A. respectively weighing the raw materials of the core layer in parts by weight: polyethylene terephthalate, hydroxyl-terminated polysiloxane emulsion, pentaerythritol adipate and filler, uniformly mixing and drying for later use; weighing the raw materials of the cortex respectively according to the parts by weight: polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer, hydroxyl-terminated polysiloxane emulsion, hexamethylene diisocyanate, ion exchange resin loaded with silver-zirconium, dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and filler, uniformly mixing and drying for later use;
B. feeding the raw materials of the core layer into a double-screw extruder to be melted into a core layer mixed melt; feeding the raw materials of the skin layer into a single-screw extruder to be melted into a skin layer mixed melt;
C. the core layer mixed melt and the skin layer mixed melt enter a composite spinning machine, are sprayed out from a composite spinneret plate after being subjected to melt distribution to form a strand silk with a skin-core structure of the core layer and the skin layer, and are subjected to air blowing cooling, stretching and winding to obtain composite fibers; the fineness of the composite fiber is 2 dtex;
D. carding the composite fibers into a web, then carrying out spunlace reinforcement and drying to obtain the elastic antibacterial non-woven fabric;
in the step B, the heating section of the double-screw extruder is 6 sections, and the heating temperature is 222 ℃, 236 ℃, 250 ℃, 260 ℃, 268 ℃ and 272 ℃ in sequence; the heating section of the single-screw extruder is 5 sections, and the heating temperature is 222 ℃, 236 ℃, 253 ℃, 265 ℃ and 275 ℃ in sequence; step D, when the mixed fibers are carded into a web, the rotating speed of a main cylinder of the carding machine is 760m/min, the rotating speed of a working roller is 60m/min, and the rotating speed of a stripping roller is 78 m/min; 5 spunlace heads are adopted for spunlacing and reinforcing the mixed fiber web; the pressure range of a plurality of the water stabs is 40 bar.
Example 3:
an elastic antibacterial non-woven fabric is prepared by composite fibers through a spunlace non-woven fabric production process;
the composite fiber has a sheath-core structure comprising a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: 0.35;
the core layer is prepared from the following raw materials in parts by weight: 100 parts of polyethylene terephthalate, 5 parts of hydroxyl-terminated polysiloxane emulsion, 3.5 parts of pentaerythritol adipate and 15 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 65 parts of polyethylene terephthalate, 35 parts of polyether polyurethane elastomer, 13 parts of maleic anhydride grafted ethylene-octene copolymer, 4.5 parts of hydroxyl-terminated polysiloxane emulsion, 5 parts of hexamethylene diisocyanate, 9 parts of silver-zirconium loaded ion exchange resin, 4 parts of dimethyloctadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and 12 parts of filler.
In this embodiment, the preparation method of the silver-zirconium loaded ion exchange resin comprises the following steps:
s1, preparing a silver-zirconium loading solution:
using silver nitrate (AgNO) 3 ) Zirconium oxynitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentrated nitric acid and deionized water to prepare silver-zirconium load solution containing 1.45mol/L silver ions, 0.26mol/L zirconium ions and 6 percent nitric acid;
s2, weighing ion exchange resin, adding the ion exchange resin into a reaction container, adding the silver-zirconium load solution which is 50 times of the ion exchange resin in weight, and stirring for 6 hours at room temperature under a 10T superconducting strong magnetic field;
s3, stopping stirring, standing for 4 hours, performing suction filtration, separating the reacted ion exchange resin, and adding the separated ion exchange resin into a 7% sodium hydroxide (NaOH) solution to be soaked for 20 min;
s4, carrying out suction filtration, separating out the ion exchange resin in the sodium hydroxide (NaOH) solution, washing the ion exchange resin to be neutral by using deionized water, drying, and crushing the ion exchange resin to be 500 meshes to obtain the silver-zirconium loaded ion exchange resin.
In this embodiment, in step S2, the ion exchange resin is a D301 type anion exchange resin.
In this example, the pH of the solution is maintained above 9 throughout the soaking process in step S3.
In this embodiment, in step S4, vacuum drying is adopted for drying, and the drying temperature is controlled at 60 ℃.
In this example, the maleic anhydride-grafted ethylene-octene copolymer had a maleic anhydride grafting ratio of 1.2%.
In this embodiment, the filler is nano calcium carbonate.
In this embodiment, the process for manufacturing the elastic antibacterial non-woven fabric includes the following steps:
A. weighing the raw materials of the core layer according to the parts by weight: polyethylene glycol terephthalate, hydroxyl-terminated polysiloxane emulsion, pentaerythritol adipate and filler are uniformly mixed and dried for later use; weighing the raw materials of the cortex respectively according to the parts by weight: polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer, hydroxyl-terminated polysiloxane emulsion, hexamethylene diisocyanate, silver-zirconium loaded ion exchange resin, dimethyl octadecyl [3- (trimethoxy silicon) propyl ] ammonium chloride and filler, uniformly mixing and drying for later use;
B. feeding the raw materials of the core layer into a double-screw extruder to be melted into a core layer mixed melt; feeding the raw materials of the skin layer into a single-screw extruder to be melted into a skin layer mixed melt;
C. the core layer mixed melt and the skin layer mixed melt enter a composite spinning machine, are sprayed out from a composite spinneret plate after being subjected to melt distribution to form a strand silk with a skin-core structure of the core layer and the skin layer, and are subjected to air blowing cooling, stretching and winding to obtain composite fibers; the fineness of the composite fiber is 5 dtex;
D. carding the composite fibers into a web, then carrying out spunlace reinforcement and drying to obtain the elastic antibacterial non-woven fabric;
wherein in the step B, the heating section of the double-screw extruder is 6 sections, and the heating temperature is 232 ℃, 242 ℃, 255 ℃, 265 ℃, 272 ℃ and 285 ℃ in sequence; the heating section of the single-screw extruder is 5 sections, and the heating temperature is 230 ℃, 246 ℃, 259 ℃, 272 ℃ and 280 ℃ in sequence; in the step D, when the mixed fibers are carded into a web, the rotating speed of a main cylinder of the carding machine is 820m/min, the rotating speed of a working roller is 68m/min, and the rotating speed of a stripping roller is 86 m/min; the number of the spunlace heads used for spunlacing and reinforcing the mixed fiber web is 9; the pressure range of a plurality of the water stabs is 48 bar.
Example 4:
an elastic antibacterial non-woven fabric is prepared by composite fibers through a spunlace non-woven fabric production process;
the composite fiber has a sheath-core structure, including a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: 0.32 of;
the core layer is prepared from the following raw materials in parts by weight: 97.5 parts of polyethylene terephthalate, 3.5 parts of hydroxyl-terminated polysiloxane emulsion, 2.8 parts of pentaerythritol adipate and 12.5 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 60 parts of polyethylene terephthalate, 32.5 parts of polyether polyurethane elastomer, 11.5 parts of maleic anhydride grafted ethylene-octene copolymer, 3.3 parts of hydroxyl-terminated polysiloxane emulsion, 4 parts of hexamethylene diisocyanate, 7.2 parts of silver-zirconium loaded ion exchange resin, 3 parts of dimethyl octadecyl [3- (trimethoxy silicon) propyl ] ammonium chloride and 10 parts of filler.
In this embodiment, the preparation method of the silver-zirconium loaded ion exchange resin comprises the following steps:
s1, preparing a silver-zirconium loading solution:
s2, weighing ion exchange resin, adding the ion exchange resin into a reaction container, adding 45 parts by weight of the silver-zirconium load solution of the ion exchange resin, and stirring for 5 hours at room temperature under a 9T superconducting strong magnetic field;
s3, stopping stirring, standing for 3 hours, performing suction filtration, separating the reacted ion exchange resin, and adding the separated ion exchange resin into a sodium hydroxide (NaOH) solution with the mass concentration of 6% to soak for 25 min;
s4, carrying out suction filtration, separating out the ion exchange resin in the sodium hydroxide (NaOH) solution, washing the ion exchange resin to be neutral by using deionized water, drying, and crushing to 300 meshes to obtain the silver-zirconium loaded ion exchange resin.
In the present embodiment, in step S1, silver nitrate (AgNO) is used 3 ) Zirconyl nitrate hydrate (ZrO (NO) 3 ) 2 ·6H 2 O), concentrated nitric acid and deionized water to prepare silver-zirconium load solution containing 1.34mol/L silver ions, 0.22mol/L zirconium ions and 5.5 percent nitric acid.
In this embodiment, in step S2, the ion exchange resin is a D301 type anion exchange resin.
In this example, the pH of the solution was maintained above 9 throughout the soaking process in step S3.
In this embodiment, in step S4, the drying is performed by vacuum drying, and the drying temperature is controlled at 56 ℃.
In this example, the maleic anhydride-grafted ethylene-octene copolymer had a maleic anhydride grafting ratio of 1.0%.
In this embodiment, the filler is nano calcium carbonate.
In this embodiment, the process for manufacturing the elastic antibacterial non-woven fabric includes the following steps:
A. respectively weighing the raw materials of the core layer in parts by weight: polyethylene glycol terephthalate, hydroxyl-terminated polysiloxane emulsion, pentaerythritol adipate and filler are uniformly mixed and dried for later use; weighing the raw materials of the cortex respectively according to the parts by weight: polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer, hydroxyl-terminated polysiloxane emulsion, hexamethylene diisocyanate, ion exchange resin loaded with silver-zirconium, dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and filler, uniformly mixing and drying for later use;
B. feeding the raw materials of the core layer into a double-screw extruder to be melted into a core layer mixed melt; feeding the raw materials of the skin layer into a single screw extruder to be melted into a skin layer mixed melt;
C. the core layer mixed melt and the skin layer mixed melt enter a composite spinning machine, are sprayed out from a composite spinneret plate after being subjected to melt distribution to form a strand silk with a skin-core structure of the core layer and the skin layer, and are subjected to air blowing cooling, stretching and winding to obtain composite fibers; the fineness of the composite fiber is 3 dtex;
D. carding the composite fibers into a web, then carrying out spunlace reinforcement and drying to obtain the elastic antibacterial non-woven fabric;
in the step B, the heating section of the double-screw extruder is 6 sections, and the heating temperature is 228 ℃, 238 ℃, 253 ℃, 262 ℃, 270 ℃ and 281 ℃ in sequence; the heating section of the single-screw extruder is 5 sections, and the heating temperature is 227 ℃, 241 ℃, 255 ℃, 269 ℃ and 278 ℃ in sequence; step D, when the mixed fibers are carded into a web, the rotating speed of a main cylinder of the carding machine is 805m/min, the rotating speed of a working roller is 64m/min, and the rotating speed of a stripping roller is 84 m/min; the number of the spunlace heads used for spunlacing and reinforcing the mixed fiber web is 7; the pressure range of a plurality of the water stabs is 44 bar.
Comparative example 1:
the difference from example 4 is that there is no hydroxyl terminated polysiloxane emulsion, and the rest is the same as example 4.
Comparative example 2:
the difference from example 4 is that no maleic anhydride-grafted ethylene-octene copolymer was present, and the rest was the same as example 4.
Comparative example 3:
the difference from example 4 is that the silver-zirconium loaded ion exchange resin was not used, and the other examples were the same as example 4.
Comparative example 4:
the difference from example 4 is that dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride is absent, and the other is the same as example 4.
Comparative example 5:
the difference from example 4 is that no silver-zirconium loaded ion exchange resin and no zirconyl nitrate hydrate were used, and the other examples were the same as example 4.
The elastic antibacterial nonwoven fabrics obtained in examples 2 to 4 of the present invention and comparative examples 1 to 5 and the common antibacterial nonwoven fabric were subjected to the following performance tests, and the test results are shown in table 1:
as can be seen from the above table, the elastic antibacterial nonwoven fabric of the present invention has the following advantages: the antibacterial property is excellent, and the antibacterial effect is good; high breaking strength and good mechanical property.
The above is only a preferred embodiment of the present invention, and it should be noted that the above preferred embodiment should not be considered as limiting the present invention, and the protection scope of the present invention should be subject to the scope defined by the claims. It will be apparent to those skilled in the art that various modifications and adaptations can be made without departing from the spirit and scope of the invention, and these modifications and adaptations should be considered within the scope of the invention.
Claims (2)
1. The manufacturing process of the elastic antibacterial non-woven fabric is characterized in that the elastic antibacterial non-woven fabric is prepared by composite fibers through a spunlace non-woven fabric production process;
the composite fiber has a sheath-core structure, including a core layer and a sheath layer; the cross section of the core layer is in a regular pentagon shape, the outer surface of the core layer is coated with the skin layer, and the cross section of the skin layer is in a circular shape; the ratio of the cross-sectional areas of the core layer and the skin layer is 1: 0.32 of;
the core layer is prepared from the following raw materials in parts by weight: 97.5 parts of polyethylene terephthalate, 3.5 parts of hydroxyl-terminated polysiloxane emulsion, 2.8 parts of pentaerythritol adipate and 12.5 parts of filler;
the skin layer is prepared from the following raw materials in parts by weight: 60 parts of polyethylene terephthalate, 32.5 parts of polyether polyurethane elastomer, 11.5 parts of maleic anhydride grafted ethylene-octene copolymer, 3.3 parts of hydroxyl-terminated polysiloxane emulsion, 4 parts of hexamethylene diisocyanate, 7.2 parts of silver-zirconium loaded ion exchange resin, 3 parts of dimethyl octadecyl [3- (trimethoxy silicon) propyl ] ammonium chloride and 10 parts of filler;
the maleic anhydride grafting rate of the maleic anhydride grafted ethylene-octene copolymer is 0.9-1.2%;
the filler is nano calcium carbonate;
the preparation method of the silver-zirconium loaded ion exchange resin comprises the following steps:
s1, preparing a silver-zirconium loading solution:
preparing silver-zirconium load solution containing 1.34mol/L silver ions, 0.22mol/L zirconium ions and 5.5% nitric acid by adopting silver nitrate, zirconyl nitrate hydrate, concentrated nitric acid and deionized water;
s2, weighing ion exchange resin, wherein the ion exchange resin is D301 type anion exchange resin, adding the ion exchange resin into a reaction container, adding 40-50 times of the silver-zirconium load solution by weight of the ion exchange resin, and stirring for 4-6 hours at room temperature under a 8-10T superconducting strong magnetic field;
s3, stopping stirring, standing for 2-4 h, performing suction filtration, separating the reacted ion exchange resin, adding the separated ion exchange resin into a sodium hydroxide solution with the mass concentration of 5-7%, and soaking for 20-30 min, wherein the pH value of the solution is kept to be higher than 9 in the whole soaking process;
s4, performing suction filtration, separating the ion exchange resin in the sodium hydroxide solution, washing the ion exchange resin with deionized water to be neutral, drying the ion exchange resin in a vacuum drying mode at the drying temperature of 50-60 ℃, and crushing the ion exchange resin to be 200-500 meshes after drying to obtain the silver-zirconium loaded ion exchange resin;
the manufacturing process of the elastic antibacterial non-woven fabric comprises the following steps:
A. weighing the raw materials of the core layer according to the parts by weight: polyethylene glycol terephthalate, hydroxyl-terminated polysiloxane emulsion, pentaerythritol adipate and filler are uniformly mixed and dried for later use; weighing the raw materials of the cortex respectively according to the parts by weight: polyethylene terephthalate, polyether polyurethane elastomer, maleic anhydride grafted ethylene-octene copolymer, hydroxyl-terminated polysiloxane emulsion, hexamethylene diisocyanate, ion exchange resin loaded with silver-zirconium, dimethyl octadecyl [3- (trimethoxysilyl) propyl ] ammonium chloride and filler, uniformly mixing and drying for later use;
B. feeding the raw materials of the core layer into a double-screw extruder to be melted into a core layer mixed melt; feeding the raw materials of the skin layer into a single screw extruder to be melted into a skin layer mixed melt;
C. the core layer mixed melt and the skin layer mixed melt enter a composite spinning machine, are sprayed out from a composite spinneret plate after being subjected to melt distribution to form strand silk with a skin-core structure of the core layer and the skin layer, and are subjected to air blowing cooling, stretching and winding to obtain composite fibers; the fineness of the composite fiber is 2-5 dtex;
D. carding the composite fibers into a web, then carrying out spunlace reinforcement and drying to obtain the elastic antibacterial non-woven fabric;
in the step B, the heating section of the double-screw extruder is 6 sections, and the heating temperature is 222-232 ℃, 236-242 ℃, 250-255 ℃, 260-265 ℃, 268-272 ℃ and 272-285 ℃ in sequence; the heating section of the single-screw extruder is 5 sections, and the heating temperature is 222-230 ℃, 236-246 ℃, 253-259 ℃, 265-272 ℃ and 275-280 ℃ in sequence; in the step D, when the mixed fibers are carded into a web, the rotating speed of a main cylinder of the carding machine is 760-820 m/min, the rotating speed of a working roller is 60-68 m/min, and the rotating speed of a stripping roller is 78-86 m/min; the number of the spunlace heads used for spunlacing and reinforcing the mixed fiber web is 5-9; the pressure range of the plurality of the water stabs is 40-48 bar.
2. An elastic antibacterial non-woven fabric manufactured by the manufacturing process of claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011204764.4A CN112342691B (en) | 2019-10-25 | 2019-10-25 | Elastic antibacterial non-woven fabric and manufacturing process thereof |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011204764.4A CN112342691B (en) | 2019-10-25 | 2019-10-25 | Elastic antibacterial non-woven fabric and manufacturing process thereof |
| CN201911020807.0A CN110670242B (en) | 2019-10-25 | 2019-10-25 | A kind of antibacterial non-woven fabric and its production process |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201911020807.0A Division CN110670242B (en) | 2019-10-25 | 2019-10-25 | A kind of antibacterial non-woven fabric and its production process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN112342691A CN112342691A (en) | 2021-02-09 |
| CN112342691B true CN112342691B (en) | 2022-09-09 |
Family
ID=69084203
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202011204764.4A Active CN112342691B (en) | 2019-10-25 | 2019-10-25 | Elastic antibacterial non-woven fabric and manufacturing process thereof |
| CN201911020807.0A Active CN110670242B (en) | 2019-10-25 | 2019-10-25 | A kind of antibacterial non-woven fabric and its production process |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201911020807.0A Active CN110670242B (en) | 2019-10-25 | 2019-10-25 | A kind of antibacterial non-woven fabric and its production process |
Country Status (1)
| Country | Link |
|---|---|
| CN (2) | CN112342691B (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111441102B (en) * | 2020-04-26 | 2022-05-13 | 浙江正凯化纤有限公司 | Preparation method of antiviral composite polyester fiber |
| CN112095230B (en) * | 2020-08-15 | 2022-09-13 | 福建冠泓工业有限公司 | Super-soft super-fluffy spun-bonded non-woven fabric and preparation method thereof |
| CN113293512A (en) * | 2021-05-22 | 2021-08-24 | 冠和卫生用品有限公司 | Antibacterial skin-friendly non-woven fabric and preparation method thereof |
| CN113981614B (en) * | 2021-12-03 | 2022-08-16 | 厦门悠派无纺布制品有限公司 | High-elasticity disposable non-woven fabric underpants and preparation method thereof |
| CN114272020B (en) * | 2021-12-24 | 2023-05-02 | 雀氏（福建）实业发展有限公司 | Preparation method of deodorizing paper diaper |
| CN119083037B (en) * | 2024-07-19 | 2026-01-02 | 博展前沿(浙江)新材料科技有限公司 | A nanofiber thermal insulation cotton and its testing device |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3635581B2 (en) * | 1993-05-10 | 2005-04-06 | 株式会社クラレ | Sustained release core-sheath composite short fiber |
| US20020187175A1 (en) * | 2001-05-08 | 2002-12-12 | Petrea Randy D. | Antimicrobial polyurethane films |
| TWI223014B (en) * | 2002-11-19 | 2004-11-01 | Ind Tech Res Inst | Functional multilobal conjugated fiber, its preparation and spinneret plate for preparing the same |
| CN1182176C (en) * | 2002-12-27 | 2004-12-29 | 济南正昊化纤新材料有限公司 | Process for preparing antibiotic polyester |
| JP5092327B2 (en) * | 2006-09-22 | 2012-12-05 | 東亞合成株式会社 | Silver inorganic antibacterial agent |
| CN101200816B (en) * | 2007-07-03 | 2010-12-01 | 赵丹青 | A quatrefoil-shaped sheath-core bicomponent fiber or filament with antibacterial and quick-drying functions |
| CN102345187B (en) * | 2011-08-02 | 2012-11-21 | 苏州东胜化纤纺织有限公司 | Antibacterial polyester fiber and preparation method thereof |
| CN102618057B (en) * | 2012-03-25 | 2014-02-05 | 徐志兵 | Ag/ion exchange resin composite material |
| CN104419150A (en) * | 2013-09-05 | 2015-03-18 | 青岛欣展塑胶有限公司 | Toughening and strengthening flame retardant antistatic modified PBT material with core-shell structure |
| CN104672816A (en) * | 2013-12-03 | 2015-06-03 | 青岛佳亿阳工贸有限公司 | Toughened and strengthened antistatic smooth PET material with core-shell structure |
| US10294608B2 (en) * | 2014-09-19 | 2019-05-21 | Sciessent Llc | Fabric treatment method |
| CN105671682B (en) * | 2014-11-17 | 2018-08-31 | 北京中纺优丝特种纤维科技有限公司 | A kind of copper system anti-bacterial fibre and preparation method thereof |
| CN104798809B (en) * | 2015-03-12 | 2016-03-09 | 江西领行药业有限公司 | A kind of organosilicon quaternary ammonium salt long acting antibiotic product and preparation method thereof |
| CN105944771A (en) * | 2016-04-27 | 2016-09-21 | 王荻 | Method for preparing large-aperture cation exchange resin containing high-valence silver ions |
| CN107938021A (en) * | 2017-10-18 | 2018-04-20 | 福建恒安卫生材料有限公司 | A kind of anti-bacterial fibre, preparation method and disposable absorbent article surface layer antibacterial non-woven |
| CN107583628A (en) * | 2017-10-27 | 2018-01-16 | 王泽山 | A kind of acetic acid takes off the production technology of iodine silver resin adsorbent |
| CN108286086B (en) * | 2018-02-08 | 2019-04-23 | 浙江银瑜新材料股份有限公司 | A new type of antibacterial PET fiber and preparation method thereof |
| CN108440738B (en) * | 2018-03-27 | 2020-11-20 | 浙江恒泰源聚氨酯有限公司 | High-elasticity antibacterial polyurethane and preparation method and application thereof |
| CN108950864A (en) * | 2018-07-27 | 2018-12-07 | 望江汇通纺织有限公司 | A kind of medical sheath core fiber non-woven fabrics of hydrophilic and oleophilic |
| CN110093681B (en) * | 2019-05-08 | 2021-11-23 | 福建省福地化纤科技有限公司 | Antibacterial ES composite short fiber for hot-air non-woven fabric surface layer and preparation method thereof |
-
2019
- 2019-10-25 CN CN202011204764.4A patent/CN112342691B/en active Active
- 2019-10-25 CN CN201911020807.0A patent/CN110670242B/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN110670242B (en) | 2020-11-27 |
| CN112342691A (en) | 2021-02-09 |
| CN110670242A (en) | 2020-01-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN112342691B (en) | Elastic antibacterial non-woven fabric and manufacturing process thereof | |
| CN110699854B (en) | Antistatic non-woven fabric and manufacturing process thereof | |
| US5124194A (en) | Hot-melt-adhesive, micro-fiber-generating conjugate fibers and a woven or non-woven fabric using the same | |
| AT503625B1 (en) | WATER-IRRADIZED PRODUCT CONTAINING CELLULASIC FIBERS | |
| US20120251597A1 (en) | End products incorporating short-cut microfibers | |
| JP2014511947A (en) | Short cut microfiber | |
| US7238313B2 (en) | Thermoplastic constructs with improved softness | |
| DE69930667T2 (en) | THERMOPLASTIC FIBERS AND TEXTILE SURFACE IMAGES | |
| CN113106631B (en) | Waterproof and oilproof elastic soft non-woven fabric and manufacturing process thereof | |
| AU2002355421A1 (en) | Thermoplastic constructs with improved softness | |
| CN104321486A (en) | Wet lap composition and related processes | |
| US6539596B1 (en) | Nonwovens from polytrimethylene terephthalate based staple fibers | |
| CN116122056A (en) | A kind of tencel fiber leather production process | |
| EP4192901A1 (en) | Sulfopolyesters comprising diethylene glycol and ethylene glycol | |
| CN105297284B (en) | A kind of manufacture method of nonwoven needled jacquard pad | |
| KR20200135018A (en) | Machine and method for preparing fibrous web, fibrillar fiber aggregate or nonwoven fabric, and fibrous web, fibrillar fiber aggregate or nonwoven fabric prepared thereby | |
| DE2325677A1 (en) | ETHYLENE / VINYL CHLORIDE / N-METHYLOLACRYLAMIDE / N- (ALCOXYMETHYL) ACRYLAMIDE | |
| KR20210030330A (en) | Machine and method for preparing fibrous web, fibrillar fiber aggregate or nonwoven fabric, and fibrous web, fibrillar fiber aggregate or nonwoven fabric prepared thereby | |
| EP4192903A1 (en) | Sulfopolyesters comprising 1,4-cyclohexanedimethanol | |
| CN114277504B (en) | Composite glue-free cotton and preparation method thereof | |
| CN120797313A (en) | Non-woven fabric manufacturing method | |
| JP2983697B2 (en) | Hydroentangled sheet, hydroentangled nonwoven fabric and method of producing hydroentangled nonwoven fabric | |
| US20230312819A1 (en) | Water-dispersible sulfopolyesters with low dispersion viscosities | |
| JPH0147585B2 (en) | ||
| DE2325731A1 (en) | ETHYLENE / VINYL CHLORIDE / N-METHYLOLACRYLAMIDE / N- (ALCOXYMETHYL) ACRYLAMIDE |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |