CN114808175A - Antibacterial and deinsectization fabric and preparation method thereof - Google Patents
Antibacterial and deinsectization fabric and preparation method thereof Download PDFInfo
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- CN114808175A CN114808175A CN202210460233.4A CN202210460233A CN114808175A CN 114808175 A CN114808175 A CN 114808175A CN 202210460233 A CN202210460233 A CN 202210460233A CN 114808175 A CN114808175 A CN 114808175A
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- Prior art keywords
- antibacterial
- deinsectization
- polypropylene
- insect
- fabric
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- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 97
- 239000004744 fabric Substances 0.000 title claims abstract description 61
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims abstract description 56
- -1 polypropylene Polymers 0.000 claims abstract description 52
- 239000004743 Polypropylene Substances 0.000 claims abstract description 48
- 229920001155 polypropylene Polymers 0.000 claims abstract description 48
- 238000006243 chemical reaction Methods 0.000 claims abstract description 31
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims abstract description 28
- 239000000126 substance Substances 0.000 claims abstract description 9
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 3
- 239000000243 solution Substances 0.000 claims description 50
- 239000000835 fiber Substances 0.000 claims description 31
- 241000238631 Hexapoda Species 0.000 claims description 30
- 238000010438 heat treatment Methods 0.000 claims description 22
- 238000001914 filtration Methods 0.000 claims description 21
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 20
- 238000001816 cooling Methods 0.000 claims description 20
- 238000001035 drying Methods 0.000 claims description 20
- 239000011777 magnesium Substances 0.000 claims description 11
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 10
- 229910052749 magnesium Inorganic materials 0.000 claims description 10
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- 239000003999 initiator Substances 0.000 claims description 9
- 230000000749 insecticidal effect Effects 0.000 claims description 9
- 238000002791 soaking Methods 0.000 claims description 9
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 239000003638 chemical reducing agent Substances 0.000 claims description 8
- JJPBKCZJVYSKGV-UHFFFAOYSA-N diethoxyphosphane Chemical compound CCOPOCC JJPBKCZJVYSKGV-UHFFFAOYSA-N 0.000 claims description 8
- 238000009987 spinning Methods 0.000 claims description 7
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 6
- 239000011261 inert gas Substances 0.000 claims description 6
- 238000001746 injection moulding Methods 0.000 claims description 6
- 229910052740 iodine Inorganic materials 0.000 claims description 6
- 239000011630 iodine Substances 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- 239000012280 lithium aluminium hydride Substances 0.000 claims description 4
- 239000012279 sodium borohydride Substances 0.000 claims description 4
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 4
- KTLIMPGQZDZPSB-UHFFFAOYSA-M diethylphosphinate Chemical compound CCP([O-])(=O)CC KTLIMPGQZDZPSB-UHFFFAOYSA-M 0.000 claims description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical class CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 17
- 150000004714 phosphonium salts Chemical group 0.000 abstract description 8
- 229920000642 polymer Polymers 0.000 abstract description 3
- 238000005406 washing Methods 0.000 description 7
- 239000003242 anti bacterial agent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 239000003814 drug Substances 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- 230000003115 biocidal effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 244000198134 Agave sisalana Species 0.000 description 2
- 235000009051 Ambrosia paniculata var. peruviana Nutrition 0.000 description 2
- 235000003097 Artemisia absinthium Nutrition 0.000 description 2
- 240000001851 Artemisia dracunculus Species 0.000 description 2
- 235000017731 Artemisia dracunculus ssp. dracunculus Nutrition 0.000 description 2
- 235000003261 Artemisia vulgaris Nutrition 0.000 description 2
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 2
- 235000017491 Bambusa tulda Nutrition 0.000 description 2
- 241001330002 Bambuseae Species 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 235000006679 Mentha X verticillata Nutrition 0.000 description 2
- 235000002899 Mentha suaveolens Nutrition 0.000 description 2
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 2
- 241001529742 Rosmarinus Species 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000001138 artemisia absinthium Substances 0.000 description 2
- 239000011425 bamboo Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 239000012496 blank sample Substances 0.000 description 2
- 210000000170 cell membrane Anatomy 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- HGXJDMCMYLEZMJ-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOOC(=O)C(C)(C)C HGXJDMCMYLEZMJ-UHFFFAOYSA-N 0.000 description 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000030833 cell death Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 238000012113 quantitative test Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007958 sleep Effects 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Images
Classifications
-
- 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
- D01F6/06—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins from polypropylene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/5036—Phosphines containing the structure -C(=X)-P or NC-P
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/40—Introducing phosphorus atoms or phosphorus-containing groups
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Textile Engineering (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Artificial Filaments (AREA)
Abstract
The invention provides an antibacterial and deinsectization fabric and a preparation method thereof, belonging to the technical field of fabrics and being prepared from antibacterial and deinsectization polypropylene, wherein the antibacterial and deinsectization polypropylene is prepared by polymerizing polypropylene and organic phosphine molecules, and the chemical structural formula of the antibacterial and deinsectization polypropylene is shown as follows; n is 100-500. One end of the organic quaternary phosphonium salt molecule is a double bond structure, and can be connected with a polypropylene polymer chain through a grafting reaction, so that the long-acting antibacterial and deinsectization effect can be achieved, the prepared antibacterial and deinsectization fabric has excellent antibacterial and deinsectization effects, can achieve the antibacterial and deinsectization effect of more than half a year, and has wide application prospect.
Description
Technical Field
The invention relates to the technical field of fabrics, and particularly relates to an antibacterial and deinsectization fabric and a preparation method thereof.
Background
With the continuous improvement of living requirements of people, more and more household articles pay more attention to comfort degree and sanitation degree on the basis of beauty; the fabric is an indispensable part in daily home furnishing, no matter the daily clothes, towels or the like, or carpets, curtains, bedsheets or the like can not be used, after the articles are used for a long time, a large amount of bacteria or microorganisms can be bred on the surface of the fabric, so that the health of a user is influenced, and the use and the attractiveness are influenced; in recent years, the situation that mite larvae damage fiber products such as fabrics is increasing, and the problem that mites inhabiting the fabrics and other articles cause allergic diseases is also increasing; because the prior art is not enough, after washing, the medicine portion can flow along with water for ordinary surface fabric that has antibiotic anti-mite medicine, thereby flows along the gap of surface fabric, thereby causes the property of a medicine that the surface fabric contains to disappear, and then influences the effect that the surface fabric was antibiotic anti-mite once more, and the sweat that flows out when the user sleeps also can take away some medicine simultaneously, causes the antibiotic anti-mite effect of this kind of surface fabric to be low.
Some technical schemes related to a preparation method of an antibacterial and anti-mite fabric also appear in the prior art, for example, a Chinese patent with the application number of CN201910539847.X discloses a preparation method of an antibacterial and anti-mite fabric, which comprises the steps of mixing wormwood fibers, mint fibers, coconut fibers, sisal fibers, bamboo fibers and rosemary fibers together by an impurity removal mixer to prepare fiber strips; then the prepared fiber strips are processed in a series of ways to prepare fiber yarns, and finally the fiber yarns and textile yarns are prepared into fabrics; according to the technical scheme, wormwood fiber, mint fiber, coconut fiber, sisal fiber, bamboo fiber and rosemary fiber are mixed together through an impurity removal mixer to prepare fiber strips serving as raw materials for preparing the antibacterial and anti-mite fabric, so that the antibacterial and anti-mite effects of the fabric are improved; however, in the technical scheme, the antibacterial and anti-mite substances in the component fibers in the fabric flow out along the gaps between the fabrics through water flow after being kneaded in the cleaning process, so that the antibacterial and anti-mite medicinal components of the fabric in the technical scheme are lost, the antibacterial and anti-mite effects of the fabric after being cleaned in the technical scheme are affected, and the limitation of the scheme is further caused.
Disclosure of Invention
The invention aims to provide an antibacterial and deinsectization fabric and a preparation method thereof, and the P of the organic quaternary phosphonium salt molecule prepared by the invention + Compared with the common quaternary ammonium salt antibacterial agent, the polarization effect and the electropositivity of the antibacterial agent are stronger, the antibacterial activity is higher, and meanwhile, the antibacterial agent also has good insect resistance. Wherein, one end of the organic quaternary phosphonium salt molecule is a double bond structure, and can be connected with the polypropylene polymer chain through a grafting reaction, so that the long-acting antibacterial and deinsectization effect can be achieved, the prepared antibacterial and deinsectization fabric has excellent antibacterial and deinsectization effects, and the antibacterial and deinsectization effect can reach more than half a yearHas wide application prospect.
The technical scheme of the invention is realized as follows:
the invention provides an antibacterial and deinsectization fabric which is prepared from antibacterial and deinsectization polypropylene, wherein the antibacterial and deinsectization polypropylene is prepared by polymerizing polypropylene and organic phosphine molecules, and the chemical structural formula of the antibacterial and deinsectization polypropylene is shown as a formula I:
n=100-500。
as a further improvement of the invention, the chemical structural formula of the organic phosphine molecule is shown as formula II:
as a further improvement of the invention, the preparation method of the organic phosphine molecule comprises the following steps:
s1, reacting chloro-tert-butane, magnesium and an initiator, adding diethyl phosphonite, and reacting to obtain an intermediate A, wherein the structure is as follows:
s2, reacting the intermediate A with a reducing agent to obtain an intermediate B, wherein the structure is as follows:
s3, reacting the intermediate B with n-butyllithium, adding methacryloyl chloride for reaction, and filtering to obtain an intermediate C, wherein the structure is as follows:
s4, adding the intermediate C into dilute hydrochloric acid, soaking for reaction, filtering, and drying to obtain the organic phosphine molecules.
As a further refinement of the invention, the initiator is iodine; the reducing agent is lithium aluminum hydride or sodium borohydride.
As a further improvement of the present invention, the ratio of the amounts of said substances of chloro-tert-butane, magnesium, diethyl phosphinate in step S1 is 1: 1: (0.3-0.4).
As a further improvement of the present invention, the ratio of the amounts of the intermediate a and the reducing agent in step S2 is 1: (1-1.2).
As a further improvement of the present invention, the ratio of the amounts of the intermediate B, n-butyllithium, and methacryloyl chloride in step S3 is 1: (1-1.2): 1.
as a further improvement of the invention, the preparation method of the organic phosphine molecule specifically comprises the following steps:
s1, under the protection of inert gas, adding an initiator and a magnesium strip into THF, dropwise adding a THF solution of chloro-tert-butane, reacting at room temperature for 2-4h, cooling to a temperature lower than 0 ℃, adding diethyl phosphonite, reacting at room temperature for 10-12h, adjusting the pH value of the solution to 6-7, filtering, and drying to obtain an intermediate A;
s2, under the protection of inert gas, cooling to the temperature of less than 0 ℃, dissolving a reducing agent in a THF solution, dropwise adding the THF solution of the intermediate A, keeping the reaction at the original temperature for 1-2h, heating and distilling to remove THF, and collecting fractions at the temperature of 150-;
s3, under the protection of inert gas, dissolving the intermediate B in a THF solution, cooling to below-70 ℃, adding the THF solution of n-butyllithium, after dropwise addition, stirring for reaction for 0.5-1h, heating to room temperature, adding the THF solution of methacryloyl chloride, stirring for reaction for 10-15h at room temperature, adding a saturated sodium bicarbonate solution, and filtering to obtain an intermediate C;
s4, adding the intermediate C into 2-4mol/L diluted hydrochloric acid, soaking for 0.5-1h for reaction, filtering, and drying to obtain the organic phosphine molecules.
As a further improvement of the invention, the preparation method of the antibacterial and insect-resistant polypropylene comprises the following steps: feeding organic phosphine molecules, an initiator and polypropylene into a screw extruder, heating to 190-.
Wherein the initiator is at least one selected from azobisisobutyronitrile, azobisisoheptonitrile, sodium bisulfite, tert-butyl hydroperoxide, benzoyl peroxide, lauroyl peroxide, cumene hydroperoxide, di-tert-butyl peroxide, tert-butyl peroxybenzoate, dicumyl peroxide, cyclohexanone peroxide, tert-butyl peroxypivalate, methyl ethyl ketone peroxide, diisopropyl peroxydicarbonate, dicyclohexyl peroxydicarbonate, sodium persulfate, potassium persulfate and ammonium persulfate.
The invention further provides a preparation method of the antibacterial and deinsectization fabric, which comprises the following steps: adding the antibacterial and insect-resistant polypropylene into a screw injection molding machine, heating, melting and spraying to obtain antibacterial and insect-resistant polypropylene fibers, preparing the antibacterial and insect-resistant polypropylene fibers into yarns, drying and spinning to obtain the antibacterial and insect-resistant fabric.
The invention has the following beneficial effects: the invention prepares an organic quaternary phosphonium salt molecule (the reaction route is shown in figure 1), and the organic quaternary phosphonium salt molecule passes through P on an antibacterial group of the organic quaternary phosphonium salt molecule + Interacts with negative charges on the surface of bacteria, adheres to the surface of thallus, sucks partial anion bacterial cell membranes into the internal gaps like anion sponge, causes wrinkling and deformation of microbial membranes, leaks intracellular substances, kills the bacteria, and simultaneously, depends on P + With Ca in the vicinity of the cell membrane 2+ 、Mg 2+ Ion exchange is performed to destroy the charge balance in the bacteria and thus to cause cell death. P of organic quaternary phosphonium salt molecule prepared by the invention + Compared with the common quaternary ammonium salt antibacterial agent, the polarization effect and the electropositivity of the antibacterial agent are stronger, the antibacterial activity is higher, and meanwhile, the antibacterial agent also has good insect resistance.
One end of the organic quaternary phosphonium salt molecule is a double bond structure, and can be connected with a polypropylene polymer chain through a grafting reaction (the reaction route is shown in figure 2), so that the long-acting antibacterial and deinsectization effect can be achieved, the prepared antibacterial and deinsectization fabric has excellent antibacterial and deinsectization effects, can achieve the antibacterial and deinsectization effect of more than half a year, and has wide application prospect.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and for those skilled in the art, other drawings can be obtained according to these drawings without creative efforts.
FIG. 1 is a schematic diagram of the synthesis scheme of the organophosphine molecule of the present invention;
FIG. 2 is a schematic diagram of the synthetic route of the antibacterial and insect-resistant polypropylene of the present invention.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1
The embodiment provides a preparation method of an antibacterial and deinsectization fabric, which specifically comprises the following steps:
(1) preparation of organic phosphine molecules:
s1. in N 2 Under protection, adding 0.1g of iodine and 1mol of magnesium strips into THF, dropwise adding 1mol of THF solution of chloro-tert-butane, reacting at room temperature for 2h, cooling to 0 ℃, adding 0.3mol of diethyl phosphonite, reacting at room temperature for 10h, adjusting the pH value of the solution to 6, filtering, and drying to obtain an intermediate A;
s2. in N 2 Under protection, cooling to 0 ℃, dissolving 1.1mol of sodium borohydride in a THF solution, dropwise adding 1mol of the THF solution of the intermediate A, keeping the original temperature for reaction for 1h, heating and distilling to remove THF, and collecting 150-155 ℃ fraction to obtain an intermediate B;
s3. in N 2 Under protection, 1mol of intermediate B is dissolved in THF solution, cooled to-78 ℃, added with 1.1mol of THF solution of n-butyl lithium, stirred and reacted for 0.5h after dropwise addition, heated to room temperature, added with 1mol of THF solution of methacryloyl chloride, stirred and reacted for 10h at room temperature, and added with saturated carbonic acidSodium hydrogen solution is filtered to obtain an intermediate C;
s4, adding the intermediate C into 2mol/L diluted hydrochloric acid, soaking for 0.5h for reaction, filtering, and drying to obtain the organic phosphine molecules.
(2) Preparing antibacterial and insect-resistant polypropylene:
feeding 10g of organic phosphine molecules, 1g of benzoyl peroxide and 100g of polypropylene into a screw extruder, heating to 190 ℃, extruding, cooling, and finally cutting into uniform antibacterial and insect-resistant polypropylene.
(3) Preparing an antibacterial and deinsectization fabric:
adding the antibacterial and insect-resistant polypropylene into a screw injection molding machine, heating, melting and spraying to obtain antibacterial and insect-resistant polypropylene fibers, preparing the antibacterial and insect-resistant polypropylene fibers into yarns, drying and spinning to obtain the antibacterial and insect-resistant fabric.
Example 2
The embodiment provides a preparation method of an antibacterial and deinsectization fabric, which specifically comprises the following steps:
(1) preparation of organic phosphine molecules:
s1. in N 2 Under protection, adding 0.1g of iodine and 1mol of magnesium strips into THF, dropwise adding 1mol of THF solution of chloro-tert-butane, reacting at room temperature for 4h, cooling to 0 ℃, adding 0.4mol of diethyl phosphonite, reacting at room temperature for 12h, adjusting the pH value of the solution to 7, filtering, and drying to obtain an intermediate A;
s2. in N 2 Under protection, cooling to 0 ℃, dissolving 1.2mol of sodium borohydride in a THF solution, dropwise adding 1mol of the THF solution of the intermediate A, keeping the original temperature for reaction for 2 hours, heating and distilling to remove THF, and collecting 150-155 ℃ fraction to obtain an intermediate B;
s3. in N 2 Under protection, dissolving 1mol of the intermediate B in a THF solution, cooling to-78 ℃, adding 1.2mol of a THF solution of n-butyllithium, after dropwise adding, stirring for reaction for 1h, heating to room temperature, adding 1mol of a THF solution of methacryloyl chloride, stirring for reaction for 15h at room temperature, adding a saturated sodium bicarbonate solution, and filtering to obtain an intermediate C;
s4, adding the intermediate C into 4mol/L diluted hydrochloric acid, soaking for 1 hour for reaction, filtering, and drying to obtain the organic phosphine molecules.
(2) Preparing antibacterial and insect-resistant polypropylene:
feeding 20g of organic phosphine molecules, 2g of tert-butyl peroxybenzoate and 100g of polypropylene into a screw extruder, heating to 210 ℃, extruding, cooling, and finally cutting into uniform antibacterial and insect-resistant polypropylene.
(3) Preparing the antibacterial and deinsectization fabric:
adding the antibacterial and insect-resistant polypropylene into a screw injection molding machine, heating, melting and spraying to obtain antibacterial and insect-resistant polypropylene fibers, preparing the antibacterial and insect-resistant polypropylene fibers into yarns, drying and spinning to obtain the antibacterial and insect-resistant fabric.
Example 3
The embodiment provides a preparation method of an antibacterial and deinsectization fabric, which specifically comprises the following steps:
(1) preparation of organic phosphine molecules:
s1. in N 2 Under protection, adding 0.1g of iodine and 1mol of magnesium strips into THF, dropwise adding 1mol of THF solution of chloro-tert-butane, reacting at room temperature for 3h, cooling to 0 ℃, adding 0.35mol of diethyl phosphonite, reacting at room temperature for 11h, adjusting the pH value of the solution to 6.5, filtering, and drying to obtain an intermediate A;
s2. in N 2 Under protection, cooling to 0 ℃, dissolving 1.15mol of lithium aluminum hydride in a THF solution, dropwise adding the THF solution of 1mol of the intermediate A, keeping the reaction at the original temperature for 1.5h, heating and distilling to remove THF, and collecting a fraction at the temperature of 150-;
s3. in N 2 Under protection, dissolving 1mol of the intermediate B in a THF solution, cooling to-78 ℃, adding 1.15mol of a THF solution of n-butyllithium, after dropwise adding, stirring for reaction for 1h, heating to room temperature, adding 1mol of a THF solution of methacryloyl chloride, stirring for reaction for 12h at room temperature, adding a saturated sodium bicarbonate solution, and filtering to obtain an intermediate C;
s4, adding the intermediate C into 3mol/L diluted hydrochloric acid, soaking for 1h for reaction, filtering, and drying to obtain the organic phosphine molecules.
(2) Preparing antibacterial and insect-resistant polypropylene:
feeding 15g of organic phosphine molecules, 1.5g of sodium persulfate and 100g of polypropylene into a screw extruder, heating to 200 ℃, extruding, cooling, and finally cutting into uniform antibacterial and insect-resistant polypropylene.
(3) Preparing the antibacterial and deinsectization fabric:
adding the antibacterial and insect-resistant polypropylene into a screw injection molding machine, heating, melting and spraying to obtain antibacterial and insect-resistant polypropylene fibers, preparing the antibacterial and insect-resistant polypropylene fibers into yarns, drying and spinning to obtain the antibacterial and insect-resistant fabric.
Comparative example 1
Compared with the example 3, the organic phosphine molecules are not grafted on the polypropylene molecular chain, and other conditions are not changed.
The method specifically comprises the following steps:
(1) preparation of organic phosphine molecules:
s1. in N 2 Under protection, adding 0.1g of iodine and 1mol of magnesium strips into THF, dropwise adding 1mol of THF solution of chloro-tert-butane, reacting at room temperature for 3h, cooling to 0 ℃, adding 0.35mol of diethyl phosphonite, reacting at room temperature for 11h, adjusting the pH value of the solution to 6.5, filtering, and drying to obtain an intermediate A;
s2. in N 2 Under protection, cooling to 0 ℃, dissolving 1.15mol of lithium aluminum hydride in a THF solution, dropwise adding the THF solution of 1mol of the intermediate A, keeping the reaction at the original temperature for 1.5h, heating and distilling to remove THF, and collecting a fraction at the temperature of 150-;
s3. in N 2 Under protection, dissolving 1mol of the intermediate B in a THF solution, cooling to-78 ℃, adding 1.15mol of a THF solution of n-butyllithium, after dropwise adding, stirring for reaction for 1h, heating to room temperature, adding 1mol of a THF solution of methacryloyl chloride, stirring for reaction for 12h at room temperature, adding a saturated sodium bicarbonate solution, and filtering to obtain an intermediate C;
s4, adding the intermediate C into 3mol/L diluted hydrochloric acid, soaking for 1h for reaction, filtering, and drying to obtain the organic phosphine molecules.
(2) Preparing the antibacterial and deinsectization fabric:
adding 100g of polypropylene and 15g of organic phosphine molecules into a screw injection molding machine, heating, melting and spinning to obtain the antibacterial and deinsectization polypropylene fiber, preparing the antibacterial and deinsectization polypropylene fiber into yarns, drying and spinning to obtain the antibacterial and deinsectization fabric.
Test example 1
The antibacterial and insecticidal fabrics prepared in examples 1 to 3 of the present invention and comparative example 1 were subjected to performance tests, and the results are shown in table 1.
The test method comprises the following steps: the antibacterial performance of the textile is evaluated by the national standard GB/T20944.3-2008 part 3: the oscillating method carries out antibacterial property quantitative test, and respectively tests the antibacterial rate of escherichia coli and the antibacterial rate of staphylococcus aureus before washing, after washing for 30 times and after being placed for half a year.
TABLE 1
The antibacterial and deinsectization fabric prepared by the method has good antibacterial performance and excellent water washing resistance, and still has excellent antibacterial performance after being placed for half a year.
Test example 2
The antibacterial and insecticidal fabrics prepared in examples 1 to 3 of the present invention and comparative example 1 were subjected to performance tests, and the results are shown in table 2.
The test method comprises the following steps: soaking the fabric in clean water, washing for 200 times, and then taking 100% cotton fabric without any treatment as a blank sample after high-temperature cooking and washing by distilled water according to GB/T24253-2009 'evaluation on anti-mite performance of textiles'. And respectively placing the washed sample and the blank sample in a culture dish, simultaneously contacting with the mites under a specified condition, after a certain period of culture, counting the live acarid bacteria in the culture dish, and calculating the mite avoidance rate or mite inhibition rate of the sample to the mites to evaluate the mite prevention effect of the sample.
After the fabric is placed for half a year, the fabric is washed for 200 times, and the anti-mite effect is tested by the same method.
TABLE 2
As can be seen from the table above, the antibacterial and deinsectization fabric prepared by the invention has good mite and deinsectization performance and excellent water washing resistance, and still has excellent mite and deinsectization performance after being placed for half a year.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.
Claims (10)
1. The antibacterial and insect-killing fabric is characterized by being prepared from antibacterial and insect-killing polypropylene, wherein the antibacterial and insect-killing polypropylene is prepared by polymerizing polypropylene and organic phosphine molecules, and the chemical structural formula of the antibacterial and insect-killing polypropylene is shown as a formula I:
n=100-500。
3. the antibacterial and insecticidal fabric according to claim 2, wherein the organic phosphine molecules are prepared by the following steps:
s1, reacting chloro-tert-butane, magnesium and an initiator, adding diethyl phosphonite, and reacting to obtain an intermediate A, wherein the structure is as follows:
s2, reacting the intermediate A with a reducing agent to obtain an intermediate B, wherein the structure is as follows:
s3, reacting the intermediate B with n-butyllithium, adding methacryloyl chloride for reaction, and filtering to obtain an intermediate C, wherein the structure is as follows:
s4, adding the intermediate C into dilute hydrochloric acid, soaking for reaction, filtering, and drying to obtain the organic phosphine molecules.
4. The antibacterial and insecticidal fabric according to claim 3, wherein the initiator is iodine; the reducing agent is lithium aluminum hydride or sodium borohydride.
5. The antibacterial and insecticidal fabric according to claim 3, wherein the amount ratio of the substances of chlorinated tert-butane, magnesium and diethyl phosphinate in step S1 is 1: 1: (0.3-0.4).
6. The antibacterial and insecticidal fabric according to claim 3, wherein the ratio of the amounts of the intermediate A and the reducing agent in step S2 is 1: (1-1.2).
7. The antibacterial and insecticidal fabric according to claim 3, wherein the ratio of the amounts of the intermediate B, n-butyllithium and methacryloyl chloride in step S3 is 1: (1-1.2): 1.
8. the antibacterial and deinsectization fabric according to claim 3, wherein the preparation method of the organic phosphine molecules is as follows:
s1, under the protection of inert gas, adding an initiator and a magnesium strip into THF, dropwise adding a THF solution of chloro-tert-butane, reacting at room temperature for 2-4h, cooling to a temperature lower than 0 ℃, adding diethyl phosphonite, reacting at room temperature for 10-12h, adjusting the pH value of the solution to 6-7, filtering, and drying to obtain an intermediate A;
s2, under the protection of inert gas, cooling to the temperature of less than 0 ℃, dissolving a reducing agent in a THF solution, dropwise adding the THF solution of the intermediate A, keeping the reaction at the original temperature for 1-2h, heating and distilling to remove THF, and collecting fractions at the temperature of 150-;
s3, under the protection of inert gas, dissolving the intermediate B in a THF solution, cooling to below-70 ℃, adding the THF solution of n-butyllithium, after dropwise addition, stirring for reaction for 0.5-1h, heating to room temperature, adding the THF solution of methacryloyl chloride, stirring for reaction for 10-15h at room temperature, adding a saturated sodium bicarbonate solution, and filtering to obtain an intermediate C;
s4, adding the intermediate C into 2-4mol/L diluted hydrochloric acid, soaking for 0.5-1h for reaction, filtering, and drying to obtain the organic phosphine molecules.
9. The antibacterial and deinsectization fabric of claim 1, wherein the antibacterial and deinsectization polypropylene is prepared by the following method: feeding organic phosphine molecules, an initiator and polypropylene into a screw extruder, heating to 190-.
10. A method of making an antibacterial insecticidal fabric according to any one of claims 1 to 9, comprising the steps of: adding the antibacterial and insect-resistant polypropylene into a screw injection molding machine, heating, melting and spraying to obtain antibacterial and insect-resistant polypropylene fibers, preparing the antibacterial and insect-resistant polypropylene fibers into yarns, drying and spinning to obtain the antibacterial and insect-resistant fabric.
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