CN106076426A - A kind of preparation method of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material - Google Patents
A kind of preparation method of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material Download PDFInfo
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- CN106076426A CN106076426A CN201610395282.9A CN201610395282A CN106076426A CN 106076426 A CN106076426 A CN 106076426A CN 201610395282 A CN201610395282 A CN 201610395282A CN 106076426 A CN106076426 A CN 106076426A
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- bioi
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 101
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 87
- 239000004753 textile Substances 0.000 title claims abstract description 57
- 239000004744 fabric Substances 0.000 title claims abstract description 53
- 239000000463 material Substances 0.000 title claims abstract description 35
- 238000006555 catalytic reaction Methods 0.000 title claims abstract description 30
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 33
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 27
- 238000006243 chemical reaction Methods 0.000 claims abstract description 19
- 239000007788 liquid Substances 0.000 claims abstract description 17
- 239000006185 dispersion Substances 0.000 claims abstract description 16
- 238000003756 stirring Methods 0.000 claims abstract description 14
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 11
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 9
- 229910017604 nitric acid Inorganic materials 0.000 claims abstract description 9
- 238000001816 cooling Methods 0.000 claims abstract description 6
- 238000001027 hydrothermal synthesis Methods 0.000 claims abstract description 6
- 239000000835 fiber Substances 0.000 claims description 44
- 238000001035 drying Methods 0.000 claims description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 10
- 238000005406 washing Methods 0.000 claims description 7
- 238000007598 dipping method Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 3
- 239000008103 glucose Substances 0.000 claims description 3
- 229920003043 Cellulose fiber Polymers 0.000 claims description 2
- 229910004878 Na2S2O4 Inorganic materials 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- 239000012279 sodium borohydride Substances 0.000 claims description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 2
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 claims description 2
- 239000012209 synthetic fiber Substances 0.000 claims description 2
- 229920002994 synthetic fiber Polymers 0.000 claims description 2
- 239000002131 composite material Substances 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 36
- 239000008367 deionised water Substances 0.000 description 11
- 229910021641 deionized water Inorganic materials 0.000 description 11
- 229910002804 graphite Inorganic materials 0.000 description 10
- 239000010439 graphite Substances 0.000 description 10
- 229920000742 Cotton Polymers 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 8
- 238000001291 vacuum drying Methods 0.000 description 8
- 239000003344 environmental pollutant Substances 0.000 description 6
- 231100000719 pollutant Toxicity 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000002351 wastewater Substances 0.000 description 6
- 229910002651 NO3 Inorganic materials 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 238000009830 intercalation Methods 0.000 description 4
- 230000002687 intercalation Effects 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 239000011941 photocatalyst Substances 0.000 description 4
- 239000012286 potassium permanganate Substances 0.000 description 4
- 239000004317 sodium nitrate Substances 0.000 description 4
- 235000010344 sodium nitrate Nutrition 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 238000010828 elution Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000002306 biochemical method Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000004042 decolorization Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 230000001699 photocatalysis Effects 0.000 description 2
- 238000013033 photocatalytic degradation reaction Methods 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 231100001234 toxic pollutant Toxicity 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- PPNKDDZCLDMRHS-UHFFFAOYSA-N bismuth(III) nitrate Inorganic materials [Bi+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PPNKDDZCLDMRHS-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000002957 persistent organic pollutant Substances 0.000 description 1
- 238000007146 photocatalysis Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
- B01J35/39—Photocatalytic properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/725—Treatment of water, waste water, or sewage by oxidation by catalytic oxidation
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/308—Dyes; Colorants; Fluorescent agents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2305/00—Use of specific compounds during water treatment
- C02F2305/10—Photocatalysts
-
- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/30—Wastewater or sewage treatment systems using renewable energies
- Y02W10/37—Wastewater or sewage treatment systems using renewable energies using solar energy
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Water Supply & Treatment (AREA)
- Environmental & Geological Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Inorganic Chemistry (AREA)
- Carbon And Carbon Compounds (AREA)
- Catalysts (AREA)
Abstract
The present invention relates to the preparation method of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material, including: textile fabric is impregnated in the saturated dispersion liquid of graphene oxide, then dry, clean, it is subsequently placed in reductant solution, 50～80 DEG C of reaction 0.5～1h, clean, dry, obtain textile fabric/Graphene；Textile fabric/Graphene is joined Bi (NO3)3And HNO3In solution, stirring, it is subsequently adding NaOH, NaBr and KI, 120～180 DEG C of hydro-thermal reaction 3～8h, wash after cooling, dry, obtain textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material.The method of the present invention is simple, is suitable for industrialized production；The composite obtaining has preferable depollution of environment effect.
Description
Technical field
The invention belongs to the preparation field of environmental catalysis material, particularly to a kind of textile fabric/Graphene/BiOBr/
The preparation method of BiOI combinational environment catalysis material.
Background technology
Environmental resource is that human society is depended on for existence the important foundation of development, and the improvement of environment and protection run through people always
The developing history of class industrial society, is directly connected to the sustainable development of human society.Shortage of water resources is that society faces
A major issue, industrial wastewater process be always environmental area the most important thing.In recent years, in actual waste water, some are low
Concentration toxic pollutant such as conjugated dye, chlorinated aromatic compound, PBDE, antibiotic etc. process and have become as the world
The focus of research.Industrial commonly used absorption and Biochemical method, toxic pollutant is simply transferred to by absorption method from liquid phase
Solid phase, is not completely eliminated organic pollution, and Biochemical method cycle length, hold facility area are big, can be organic because of dyestuff etc.
Biological toxic action can not effectively be removed by thing.By comparison, high-level oxidation technology is by producing the work of strong oxidizing property
Property kind can directly the organic matters such as dyestuff effectively be degraded, even thorough mineralising, cause the extensive concern of people, but these senior oxygen
Change technology also has certain limitation, and as easily brought secondary pollution, processing cost is high, be not suitable for the process of big flow waste water and in a large number
In the presence of organic/inorganic compound, the preferential removal to toxic target pollutant is extremely difficult, therefore designs and develops a kind of efficient
The catalyst system and catalyzing removing toxic target pollutant in actual waste water system has great importance.
In order at the efficient micro-nano structure of textile fabric surface construction, and overcome the using to catalysis fibre performance of adhesive
Harmful effect, researcher attempts utilizing sol-gel dressed method to prepare catalysis fiber, and result of study shows prepared by this method
Catalysis fibre have certain catalytic performance, but there is following problems: the solidification of (1) gel at high temperature to be carried out, right
The physical and mechanical properties of textile fabric has an impact, as bigger in tearing brute force loss；(2) what prepared by sol-gel process is unglazed urging
Change the unbodied nano-photocatalyst of performance, therefore to make it to required crystal transfer by certain approach, and crystalline phase need to be improved
Degree of crystallinity, reduce lattice defect；(3) high temperature sintering is that current amorphous phase changes to sizing and raising degree of crystallinity is most common
Method, but its calcining heat typically wants the temperature of 300 DEG C or more to realize, it is clear that conventional textile fibers can not bear as
This high temperature, this is that sol-gal process is applied to common problem during organic supporting substrates；(4) photochemical catalyst and fibre
Tieing up direct contact can make fiber generation photooxidative degradation, and result causes the physical and mechanical properties of textile fabric to decline.Therefore the party
The application of method is extremely restricted.Under cryogenic, it is achieved nano-photocatalyst is worked as from amorphous to being converted into of setting
Front study hotspot.The solution of this difficult problem, is to seek a kind of low temperature system that can walk around high temperature crystal growth and phase transformation link
The method of standby high efficiency photocatalyst, is then processed to textile fabric again.Low temperature process is to use presoma to be that presoma passes through
Sol-gel technique prepares stable sol, and then fabricated in situ is to fiber surface, realizes nanometer in 100 DEG C of boiling water on fiber
Photochemical catalyst is from amorphous state to the transformation of sizing state, and catalysis fiber prepared by the method is only functional, and application is convenient,
There is textile fabric by photooxidative degradation, the problems such as strength loss is big.By increasing burning on fibrous material further
The approach of thing load capacity improves its photocatalysis performance, will cause the serious reunion of metal oxide, and affecting catalysis material can profit
Effective ratio area, change textile fabric/metal oxide materials loose structure, be unfavorable for organic pollutant at fibre
Dimension material surface enrichment, also will affect the catalytic performance of catalysis material simultaneously.
Content of the invention
The technical problem to be solved is to provide a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment
The preparation method of catalysis material, the method is simple, low cost, non-secondary pollution, it is easy to industrialized production；The composite obtaining
There is preferable depollution of environment effect.
A kind of preparation method of the textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material of the present invention, bag
Include:
(1) being impregnated into textile fabric in the saturated dispersion liquid of graphene oxide, 60～80 DEG C of drying, repeated impregnations is dried
2～3 times, clear water washs, and is subsequently placed in reductant solution, 50～80 DEG C of reaction 0.5～1h, makes the graphite oxide of fabric face
Alkene is reduced to Graphene, cleans, and dries, obtains textile fabric/Graphene；
(2) textile fabric/Graphene in step (1) is joined Bi (NO3)3And HNO3In solution, stirring, then add
Enter NaOH, NaBr and KI, 120～180 DEG C of hydro-thermal reaction 3～8h, after cooling wash, dry, obtain textile fabric/Graphene/
BiOBr/BiOI combinational environment catalysis material.
Remove fiber surface impurity by acetone treatment before textile fabric uses in described step (1), be then vacuum dried；Oxygen
Functionalized graphene is to be prepared by Hummers method；Textile fabric be textile fabric be cellulose fibre, protein fibre
Or, regenerated fiber, synthetic fibers or the fiber that wherein any two kinds or three kinds of fiber blends are made.
Described textile fabric is flaxen fiber, cotton fiber or silk fiber.
The preparation method of described graphene oxide: 230～250mL concentrated sulfuric acid and 3～6g sodium nitrate are added in beaker, ice
Water-bath cools down, the lower 10g graphite powder that adds of stirring, to be mixed uniformly after, be slowly added to after 30～50g potassium permanganate is finely ground, at 0 DEG C
Stirring reaction 1～2h, obtains graphite intercalation compound；It is warmed up to 35～45 DEG C to continue after reaction 30～60min, add 460～
600mL deionized water, continues reaction 30～45min；Sequentially add 1400～1800mL deionized water and 30～60ml mass
Fraction 30% hydrogen peroxide, solution becomes vivid yellow from brick-red, after continuing reaction 10～25min, filters, dilute with 2～4%
Salt acid elution, then repeatedly centrifuges (8000rpm, 30～45min) washing, 50～70 DEG C of vacuum dryings, obtains by deionized water
Graphene oxide is re-dispersed in water by graphene oxide, ultrasonic 30～50min, by dispersion liquid in vacuum drying chamber 40
Dry moisture for～60 DEG C and obtain graphene oxide.
In described step (1), the concentration of the saturated dispersion liquid of graphene oxide is 0.5～2mg/mL；The solvent of dispersion liquid is
Water.
In described step (1), reducing agent is NaBH4、Na2S2O4, HI and N2H4Or glucose.
In described step (1), the bath raio of dipping is 15:1～6:1；The time of dipping is 15～30min.
Cleaning in described step (1) is: wash 2～3 times with warm water, to remove the reducing agent of surface adhesion；Dry temperature
Degree is 60 DEG C.
Bi (NO in described step (2)3)3Mass ratio with textile fabric/Graphene is 1:20～1:50.
In described step (2), the mass ratio of textile fabric/Graphene and NaOH is 1:20～1:50.
Textile fabric/Graphene and HNO in described step (2)3Mass ratio be 1:100～1:200.
In described step (2), the quality of textile fabric/Graphene and the quality sum of NaBr and KI are than for 1:200～1:
300；Wherein, the mass ratio of NaBr and KI is 1:1～1:5.
In described step (2), washing is for being washed with deionized 3 times；Drying temperature is 60 DEG C.
The present invention utilizes the Graphene with high-specific surface area and high conduction performance three-dimensional even at textile fabric surface construction
Continuous conductive network.Construct the Nano semiconductor material with controllable appearance, composition, size and loose structure on this basis further
Material, thus form novel textile fabric/Graphene/heterogeneous semiconductor continuous grids structure, utilize flexible fibrous material many
Permeability and capillary effect, make fiber can adsorb pollutant, simultaneously again can be by absorption pollutant in fiber surface enrichment
There is provided high concentration reactant bad border for nano-photocatalyst material, this accelerates photocatalytic degradation reaction rate to a great extent.
Additionally, the intermediate by-products that the suction-operated of fiber is also possible to make photocatalytic degradation reaction produce is adsorbed and quilt when generating
It is degraded to simple inorganic matter further, such as carbon dioxide and water.So fiber can not only concentrate pollutant, accelerates light
Catalytic degradation reaction, and intermediate by-products can be reduced, timely releasing product, constantly advance degradation reaction.Simultaneously also abundant
Playing high-specific surface area and high conduction performance effective discrete nucleation material of Graphene, increase catalyst contacts with pollutant
Interface, provides more reactivity point for light-catalyzed reaction, and guarantees to realize the directional transmissions of light induced electron, effectively carries
High its with hole separative efficiency, improve its photocatalytic activity.
Beneficial effect
(1) preparation method of the present invention is simple, low cost, does not increase new equipment, it is easy to industrialized production；
(2) the composite catalyzing material catalytic performance of the preparation of the present invention is good, and degradation rate more than 95% can be recycled.
Detailed description of the invention
Below in conjunction with specific embodiment, the present invention is expanded on further.Should be understood that these embodiments are merely to illustrate the present invention
Rather than restriction the scope of the present invention.In addition, it is to be understood that after having read the content that the present invention lectures, people in the art
The present invention can be made various changes or modifications by member, and these equivalent form of values fall within the application appended claims equally and limited
Scope.
Embodiment 1
(1) adding in beaker by the 230mL concentrated sulfuric acid and 3g sodium nitrate, ice-water bath cools down, and stirring is lower adds 10g graphite powder,
To be mixed uniformly after, be slowly added to after 30g potassium permanganate is finely ground, at 0 DEG C, stirring reaction 1h, obtains graphite intercalation compound；Rise
After temperature to 35 DEG C continues reaction 30min, add 460mL deionized water, continue reaction 30min；Sequentially add 1400mL go from
Sub-water and 30ml 30% hydrogen peroxide, solution becomes vivid yellow from brick-red, after continuing reaction 10min, filters, dilute with 2%
Salt acid elution, then repeatedly centrifuges (8000rpm, 30min) washing, 50 DEG C of vacuum dryings, obtains graphite oxide by deionized water
Graphene oxide is re-dispersed in water by alkene, ultrasonic 30min, and by dispersion liquid, in vacuum drying chamber, 40 DEG C of drying moisture obtain
To graphene oxide；
(2) choose flaxen fiber to remove fiber surface impurity as carrier, use acetone soln, be then vacuum dried.Take oxygen
Graphite ultrasonic disperse in water, preparation concentration is the saturated dispersion liquid of graphene oxide of 0.5mg/mL.By the textile leaching of 2g
Stain, to the saturated dispersion liquid 30mL of graphene oxide, impregnates latter 60 DEG C drying, and repeated impregnations is dried 2 times, and clear water washs.By above-mentioned
The textile that graphene oxide was processed is placed in the NaBH containing 2g4It in solution, is warming up to 50 DEG C, react 0.5h, make fabric table
The graphene oxide in face is reduced to Graphene.Then wash 2 times with warm water, to remove the reducing agent of surface adhesion, 60 DEG C of drying,
Obtain flaxen fiber/Graphene.
(3) flaxen fiber/grapheme material obtaining in step (2) is joined Bi (NO3)3And HNO3In solution, magnetic force stirs
Mix 30min, then in solution, add NaOH and NaBr and KI, 120 DEG C of hydro-thermal reactions 3h.Naturally, after cooling down, deionized water is used
Wash 3 times, 60 DEG C of drying, the three-dimensional combinational environment catalysis material of synthesis flaxen fiber/Graphene/BiOBr/BiOI.Wherein, fiber crops are fine
Dimension/Graphene and HNO3Mass ratio be 1:200；Bi(NO3)3Mass ratio with flaxen fiber/Graphene is 1:50；Flaxen fiber/stone
The mass ratio of ink alkene and NaOH is 1:50；The quality sum of the quality of flaxen fiber/Graphene and NaBr and KI is than for 1:300；Its
In, the mass ratio of NaBr and KI is 1:1.
Embodiment 2
(1) adding in beaker by the 240mL concentrated sulfuric acid and 4.5g sodium nitrate, ice-water bath cools down, and stirring is lower adds 10g graphite
Powder, to be mixed uniformly after, be slowly added to after 40g potassium permanganate is finely ground, stirring reaction 1.5h at 0 DEG C, obtain graphite intercalation and be combined
Thing；After being warmed up to 40 DEG C of continuation reaction 45min, add 530mL deionized water, continue reaction 37min；Sequentially add 1600mL
Deionized water and 45ml 30% hydrogen peroxide, solution becomes vivid yellow from brick-red, after continuing reaction 18min, filters, uses
3% watery hydrochloric acid washing, then repeatedly centrifuges (8000rpm, 37min) washing, 60 DEG C of vacuum dryings, is aoxidized by deionized water
Graphene oxide is re-dispersed in water by Graphene, ultrasonic 340min, by dispersion liquid in vacuum drying chamber 50 DEG C dry water
Get graphene oxide；
(2) choose cotton fiber to remove fiber surface impurity as carrier, use acetone soln, be then vacuum dried.Take oxygen
Graphite ultrasonic disperse in water, the saturated dispersion liquid of graphene oxide of preparation concentration 1.2mg/mL.By the textile leaching of 2.5g
Stain, to the saturated dispersion liquid 25mL of graphene oxide, impregnates latter 70 DEG C drying, and repeated impregnations is dried 2 times, and clear water washs.By above-mentioned
The textile that graphene oxide was processed is placed in the glucose solution containing 2.5g, is warming up to 65 DEG C, reacts 0.75h, makes to knit
The graphene oxide on thing surface is reduced to Graphene.Then wash 2 times with warm water, to remove the reducing agent of surface adhesion, 60 DEG C
Dry, obtain cotton fiber/Graphene.
(3) cotton fiber/grapheme material is joined Bi (NO3)3And HNO3In solution, magnetic force stirs 30min, then to solution
Middle addition appropriate NaOH and NaBr and KI, 150 DEG C of hydro-thermal reactions 5.5h.Naturally it, after cooling down, is washed with deionized 3 times,
60 DEG C of drying, the three-dimensional combinational environment catalysis material of synthesis cotton fiber/Graphene/BiOBr/BiOI.Wherein, Bi (NO3)3Fine with cotton
The mass ratio of dimension/Graphene is 1:30；The mass ratio of cotton fiber/Graphene and NaOH is 1:30；Cotton fiber/Graphene and HNO3
Mass ratio be 1:150；The quality sum of the quality of cotton fiber/Graphene and NaBr and KI is than for 1:250；Wherein, NaBr and
The mass ratio of KI is 1:2.
Embodiment 3
(1) adding in beaker by the 250mL concentrated sulfuric acid and 6g sodium nitrate, ice-water bath cools down, and stirring is lower adds 10g graphite powder,
To be mixed uniformly after, be slowly added to after 50g potassium permanganate is finely ground, at 0 DEG C, stirring reaction 2h, obtains graphite intercalation compound；Rise
After temperature to 45 DEG C continues reaction 60min, add 600mL deionized water, continue reaction 45min；Sequentially add 1800mL go from
Sub-water and 60ml 30% hydrogen peroxide, solution becomes vivid yellow from brick-red, after continuing reaction 25min, filters, dilute with 4%
Salt acid elution, then repeatedly centrifuges (8000rpm, 45min) washing, 70 DEG C of vacuum dryings, obtains graphite oxide by deionized water
Graphene oxide is re-dispersed in water by alkene, ultrasonic 50min, and by dispersion liquid, in vacuum drying chamber, 60 DEG C of drying moisture obtain
To graphene oxide；
(2) choose silk fiber to remove fiber surface impurity as carrier, use acetone soln, be then vacuum dried.Take
Appropriate graphite oxide ultrasonic disperse in water, prepares the saturated dispersion liquid of the dense graphene oxide for 2mg/mL.By the textile of 3g
Being impregnated into the saturated dispersion liquid 18mL of graphene oxide, impregnating latter 80 DEG C drying, repeated impregnations is dried 3 times, and clear water washs.By upper
State the textile that graphene oxide processed and be placed in the Na containing 3g2S2O4It in solution, is warming up to 80 DEG C, react 1h, make fabric table
The graphene oxide in face is reduced to Graphene.Then wash 3 times with warm water, to remove the reducing agent of surface adhesion, 60 DEG C of drying,
Obtain silk fiber/Graphene.
(3) silk fiber/grapheme material is joined Bi (NO3)3And HNO3In solution, magnetic force stirs 30min, then to molten
Liquid adds appropriate NaOH and NaBr and KI, 180 DEG C of hydro-thermal reactions 8h.Naturally it, after cooling down, is washed with deionized 3 times,
60 DEG C of drying, the three-dimensional combinational environment catalysis material of synthesis silk fiber/Graphene/BiOBr/BiOI.
Wherein, the Bi (NO described in step (3)3)3Mass ratio with silk fiber/Graphene is 1:20；Silk fiber/
The mass ratio of Graphene and NaOH is 1:20；Silk fiber/Graphene described in step (3) and HNO3Mass ratio be 1:
100；In step (3), the quality of silk fiber/Graphene and the quality sum of NaBr and KI are than for 1:200；Wherein, NaBr and KI
Mass ratio be 1:5.
With the same time sampling printing and dyeing mill dyeing waste water for process object, the embodiment 1 being separately added in waste water
The water treatment agent of～3 gained, after 2 hours solar radiations, water treatment agent is as shown in table 1 to the percent of decolourization of dyeing waste water: table 1
| Percent of decolourization | COD clearance | |
| Embodiment 1 | 99.6% | 90.2% |
| Embodiment 2 | 99.1% | 90.3% |
| Embodiment 3 | 99.5% | 90.6% |
Claims (10)
1. the preparation method of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material, comprising:
(1) it is impregnated into textile fabric in the saturated dispersion liquid of graphene oxide, then dries, clean, be subsequently placed in reducing agent
In solution, 50～80 DEG C of reaction 0.5～1h, clean, dry, obtain textile fabric/Graphene；
(2) textile fabric/Graphene in step (1) is joined Bi (NO3)3And HNO3In solution, stirring, it is subsequently adding
NaOH, NaBr and KI, 120～180 DEG C of hydro-thermal reaction 3～8h, after cooling wash, dry, obtain textile fabric/Graphene/
BiOBr/BiOI combinational environment catalysis material.
2. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that in described step (1), textile fabric uses front acetone treatment, is then vacuum dried；Graphene oxide
It is to be prepared by Hummers method；Textile fabric be cellulose fibre, protein fibre, regenerated fiber, synthetic fibers or
Person's fiber that wherein any two or more fiber blend is made.
3. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that in described step (1), the concentration of the saturated dispersion liquid of graphene oxide is 0.5～2mg/mL.
4. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that in described step (1), reducing agent is NaBH4、Na2S2O4、HI、N2H4Or the one in glucose.
5. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that in described step (1), the bath raio of dipping is 15:1～6:1；The time of dipping is 15～30min.
6. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that Bi (NO in described step (2)3)3Mass ratio 1:20～1:50 with textile fabric/Graphene.
7. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that the mass ratio 1:20～1:50 of textile fabric/Graphene and NaOH in described step (2).
8. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that textile fabric/Graphene and HNO in described step (2)3Mass ratio 1:100～1:200.
9. the preparation of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Method, it is characterised in that in described step (2), the quality of textile fabric/Graphene and the quality sum ratio of NaBr and KI are 1:
200～1:300；Wherein, the mass ratio of NaBr and KI is 1:1～1:5.
10. the system of a kind of textile fabric/Graphene/BiOBr/BiOI combinational environment catalysis material according to claim 1
Preparation Method, it is characterised in that in described step (2), washing is for being washed with deionized 3 times；Drying temperature is 60 DEG C.
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| CN112647289A (en) * | 2020-12-17 | 2021-04-13 | 上海城建职业学院 | Preparation method of yarn protection type flexible photocatalytic fabric |
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| CN106732789A (en) * | 2016-12-02 | 2017-05-31 | 东华大学 | A kind of fiber/CNT/AgBiOX three-dimensional recyclable efficient catalytic material and its preparation and application |
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| CN108355717A (en) * | 2018-01-16 | 2018-08-03 | 齐鲁工业大学 | A kind of preparation method of cellulose/BiOBr composite photocatalyst materials |
| CN109569673A (en) * | 2018-12-26 | 2019-04-05 | 江苏泷膜环境科技有限公司 | A kind of preparation method of the defect BiOI-BiOBr composite photocatalyst material with excellent photocatalysis performance |
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| CN110624574A (en) * | 2019-09-09 | 2019-12-31 | 常州大学 | Double Bi4O5I2Preparation method of photocatalytic material and application of photocatalytic material in degrading MC-LR |
| CN110624574B (en) * | 2019-09-09 | 2022-03-25 | 常州大学 | Double Bi4O5I2Preparation method of photocatalytic material and application of photocatalytic material in degrading MC-LR |
| CN112647289A (en) * | 2020-12-17 | 2021-04-13 | 上海城建职业学院 | Preparation method of yarn protection type flexible photocatalytic fabric |
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