CN106256430A - A kind of preparation method of the bismuth oxychloride/graphene composite photocatalyst of tin dope - Google Patents
A kind of preparation method of the bismuth oxychloride/graphene composite photocatalyst of tin dope Download PDFInfo
- Publication number
- CN106256430A CN106256430A CN201610663248.5A CN201610663248A CN106256430A CN 106256430 A CN106256430 A CN 106256430A CN 201610663248 A CN201610663248 A CN 201610663248A CN 106256430 A CN106256430 A CN 106256430A
- Authority
- CN
- China
- Prior art keywords
- solution
- bismuth oxychloride
- tin dope
- water
- graphene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 38
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 title claims abstract description 37
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 title claims abstract description 36
- 229940073609 bismuth oxychloride Drugs 0.000 title claims abstract description 35
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 35
- 239000011941 photocatalyst Substances 0.000 title claims abstract description 30
- 239000002131 composite material Substances 0.000 title claims abstract description 25
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- 239000000243 solution Substances 0.000 claims abstract description 56
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 36
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 27
- 238000003756 stirring Methods 0.000 claims abstract description 25
- 239000003054 catalyst Substances 0.000 claims abstract description 19
- 239000011259 mixed solution Substances 0.000 claims abstract description 11
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims abstract description 9
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 claims abstract description 9
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 claims abstract description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 239000002351 wastewater Substances 0.000 claims description 17
- 238000001035 drying Methods 0.000 claims description 15
- 238000001914 filtration Methods 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 8
- 150000001336 alkenes Chemical class 0.000 claims description 7
- 238000005352 clarification Methods 0.000 claims description 7
- 239000004575 stone Substances 0.000 claims description 4
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 claims description 3
- 229940043267 rhodamine b Drugs 0.000 claims description 3
- 230000001105 regulatory effect Effects 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229910000416 bismuth oxide Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 claims 1
- 230000001699 photocatalysis Effects 0.000 abstract description 10
- 238000007146 photocatalysis Methods 0.000 abstract description 8
- 239000007864 aqueous solution Substances 0.000 abstract description 7
- 239000000975 dye Substances 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- -1 aromatic halide Chemical class 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 206010002660 Anoxia Diseases 0.000 description 1
- 241000976983 Anoxia Species 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- 208000031320 Teratogenesis Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 230000007953 anoxia Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000013033 photocatalytic degradation reaction Methods 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/135—Halogens; Compounds thereof with titanium, zirconium, hafnium, germanium, tin or lead
-
- B01J35/19—
-
- B01J35/39—
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/009—Preparation by separation, e.g. by filtration, decantation, screening
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/03—Precipitation; Co-precipitation
- B01J37/031—Precipitation
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/34—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation
- B01J37/341—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation making use of electric or magnetic fields, wave energy or particle radiation
- B01J37/343—Irradiation by, or application of, electric, magnetic or wave energy, e.g. ultrasonic waves ; Ionic sputtering; Flame or plasma spraying; Particle radiation making use of electric or magnetic fields, wave energy or particle radiation of ultrasonic wave energy
-
- 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
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/281—Treatment of water, waste water, or sewage by sorption using inorganic sorbents
-
- 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
-
- 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
Abstract
The invention discloses the preparation method of the bismuth oxychloride/graphene composite photocatalyst of a kind of tin dope, concretely comprise the following steps: (1) is by Bi (NO3)3·5H2O is dissolved in obtained solution X in hydrochloric acid solution;(2) by SnCl2·2H2O agitating heating is dissolved in hydrochloric acid solution and obtains transparent settled solution Y;(3) under stirring, solution X is dropwise instilled in solution Y, be 6 with the pH value of the sodium hydroxide solution regulation mixed solution that molar concentration is 2mol/L;(4) the bismuth oxychloride visible light catalyst of tin dope is prepared in 60 DEG C of dry 5h;(5) aqueous solution at Graphene adds the bismuth oxychloride visible light catalyst of tin dope, prepares the bismuth oxychloride/graphene composite photocatalyst of tin dope in 60 DEG C of dry 5h.The bismuth oxychloride of the tin dope that the present invention prepares/Graphene composite visible light catalyst has preferable absorbing properties, and has visible light-responded photocatalysis performance.
Description
Technical field
The invention belongs to photocatalyst and dye wastewater degradation technical field, be specifically related to the oxychloride of a kind of tin dope
The preparation method of bismuth/graphene composite photocatalyst.
Background technology
The development of society, promotes the development of chemical industry, but industrial wastewater is also constantly in evolution
Increase.Waste water from dyestuff is one of main noxious industry waste water, is mainly derived from dye and dye intermediate production industry.Dyestuff
Of a great variety, substantial amounts of waste water from dyestuff is discharged in environment water, causes the pollution to natural water.First, waste water from dyestuff
Colourity is bigger, it is possible to absorb light, reduces the transparency of water body, causes anoxia in water, very big to microbiological effect in water body,
Destroy the self-purification of water;Secondly, dyestuff is raw after organic aromatic compound benzene ring hydrogen is replaced by halogen, nitro, amido
Many phenyl ring substituted compounds such as the aromatic halide of one-tenth, aromatic nitro compound, aromatic amine chemicals, biphenyl, poison
Property the biggest, the harm that can produce " teratogenesis, carcinogenic, mutagenesis " that has, in waste water, content of organics is high, complicated component,
Harmful substance contents is high.Due to the bio-refractory of waste water from dyestuff, semi-conducting material photocatalysis oxidation technique is closed increasingly
Note, it has also become study hotspot both domestic and external.Recently coming, bismuth system catalysis material gets more and more people's extensive concerning, as one
Important BiOX, BiOCl is a kind of novel polynary bismuth metal oxide photocatalyst, due to its suitable forbidden band width
Degree, special layer structure and there is good photocatalytic activity and enjoy pass, but, the photocatalytic of a kind of semi-conducting material
Can be not only relevant with the optical property of photocatalyst, important relation is also had with light source.Generally, urge higher than light when photon energy
During the energy gap of agent, the preferable photocatalysis effect of photocatalyst competence exertion, illumination is the strongest, and photocatalysis performance is the best.Carry
The photocatalysis effect of high photocatalyst can be in terms of the character two of the utilization rate and change catalysis material that improve nature light
Consider.
Graphene be a kind of energy gap be the semimetal of zero, in photocatalysis field, due to Graphene, to have the electronics of uniqueness special
Property, great specific surface area and higher transparency become the ideal carrier of synthesis composite photo-catalyst, the electricity of Graphene
Transport factor is the highest, utilizes Graphene to be modified photocatalyst, not only can realize broadband light and absorb, but also
Electric charge can be made more to mate with catalyst in transfer process, improve its photocatalysis performance;Next to that Graphene has uniqueness
Two-dimensional surface structure and there is bigger specific surface area, can induce when forming complex to produce and the strong absorption of pollutant is made
With, beneficially the carrying out further of photocatalytic degradation.
Summary of the invention
Present invention solves the technical problem that there is provided one can the stannum of effective rhodamine B degradation (RhB) waste water from dyestuff
The preparation method of the bismuth oxychloride/graphene composite photocatalyst of doping.
The present invention solves that above-mentioned technical problem adopts the following technical scheme that, the bismuth oxychloride/stone of a kind of tin dope
The preparation method of ink alkene composite photo-catalyst, it is characterised in that concretely comprise the following steps: (1) is by 1mmol Bi (NO3)3·5H2O dissolves
Obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;(2) by 1mmol SnCl2·2H2O agitating heating is dissolved
Transparent settled solution Y is obtained in the hydrochloric acid solution that 40mL molar concentration is 1mol/L;(3) under stirring, by solution X by
Instill in solution Y, after continuing stirring 30min, regulate the pH of mixed solution with the sodium hydroxide solution that molar concentration is 2mol/L
Value is 6;(4) continuing stirring 2h after the pH value of complete mixed solution to be regulated, sucking filtration is precipitated thing, respectively washes three with water and ethanol
Secondary, in thermostatic drying chamber, the bismuth oxychloride visible light catalyst of tin dope is then prepared in 60 DEG C of dry 5h;(5) by 0.625-
Obtaining the aqueous solution of Graphene in the 5mg graphene oxide ultrasonic 50mL of being dissolved in water, the bismuth oxychloride adding 1g tin dope is visible
Photocatalyst, ultrasonic disperse 30min, it is stirred for 2h, sucking filtration is precipitated thing, respectively washes three times with water and ethanol, then at constant temperature
Drying baker prepares the bismuth oxychloride/graphene composite photocatalyst of tin dope in 60 DEG C of dry 5h.
Further preferably, in step (5), the addition of graphene oxide is preferably 2.5mg, and the stannum prepared under the conditions of being somebody's turn to do is mixed
The rhodamine B of degraded rhdamine B waste water 3h under natural sunlight goes miscellaneous bismuth oxychloride/graphene composite photocatalyst
Except rate is 99.91%.
The bismuth oxychloride of the tin dope that the present invention prepares/Graphene composite visible light catalyst has preferable light absorption
Can, and there is visible light-responded photocatalysis performance, there is under sunlight the property of efficient degradation rhdamine B waste water
Can, absorption spectrum ranges width, stable performance, nontoxic and cost effective, it is possible to be applied to the fall of difficult for biological degradation organic pollution
Solve, there is stronger market application foreground.
Detailed description of the invention
By the following examples the foregoing of the present invention is described in further details, but this should be interpreted as this
The scope inventing above-mentioned theme is only limitted to below example, and all technology realized based on foregoing of the present invention belong to this
Bright scope.
Embodiment 1
By 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;Will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;Under stirring, solution X is dropwise instilled in solution Y, continue stirring 30min, be the hydrogen of 2mol/L by molar concentration
The pH value of sodium hydroxide solution regulation mixed solution is 6, continues stirring 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol,
Then in thermostatic drying chamber, the bismuth oxychloride visible light catalyst of tin dope is prepared in 60 DEG C of dry 5h.This visible light catalyst
Under natural sunlight, the RhB clearance of degraded rhdamine B waste water 3h is 83.39%.
Embodiment 2
By 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;Will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;Under stirring, solution X is dropwise instilled in solution Y, continue stirring 30min, be the hydrogen of 2mol/L by molar concentration
The pH value of sodium hydroxide solution regulation mixed solution is 6, continues stirring 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol,
Then in thermostatic drying chamber, prepare the bismuth oxychloride visible light catalyst of tin dope in 60 DEG C of dry 5h, 0.625mg is aoxidized
The Graphene ultrasonic 50mL of being dissolved in water obtains the aqueous solution of Graphene, adds the bismuth oxychloride visible light catalytic of 1g tin dope
Agent, ultrasonic disperse 30min, it is stirred for 2h, sucking filtration is precipitated thing, respectively washes three times with water and ethanol, then at thermostatic drying chamber
In prepare the bismuth oxychloride/graphene composite photocatalyst containing 0.0625wt% tin dope in 60 DEG C of dry 5h.This complex light is urged
Agent RhB clearance of degraded rhdamine B waste water 3h under natural sunlight is 88.21%.
Embodiment 3
By 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;Will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;Under stirring, solution X is dropwise instilled in solution Y, continue stirring 30min, be the hydrogen of 2mol/L by molar concentration
The pH value of sodium hydroxide solution regulation mixed solution is 6, continues stirring 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol,
Then in thermostatic drying chamber, the bismuth oxychloride visible light catalyst of tin dope is prepared in 60 DEG C of dry 5h;1.25mg is aoxidized stone
The ink alkene ultrasonic 50mL of being dissolved in water obtains the aqueous solution of Graphene, adds the bismuth oxychloride visible light catalyst of 1g tin dope,
Ultrasonic disperse 30min, is stirred for 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol, then in thermostatic drying chamber in
60 DEG C of dry 5h i.e. prepare the bismuth oxychloride/graphene composite photocatalyst containing 0.125wt% tin dope.This composite photocatalyst
Agent RhB clearance of degraded rhdamine B waste water 3h under natural sunlight is 98.46%.
Embodiment 4
By 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;Will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;Under stirring, solution X is dropwise instilled in solution Y, continue stirring 30min, be the hydrogen of 2mol/L by molar concentration
The pH value of sodium hydroxide solution regulation mixed solution is 6, continues stirring 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol,
Then in thermostatic drying chamber, the bismuth oxychloride visible light catalyst of tin dope is prepared in 60 DEG C of dry 5h;Take 2.5mg and aoxidize stone
The ink alkene ultrasonic 50mL of being dissolved in water obtains the aqueous solution of Graphene, adds the bismuth oxychloride visible light catalyst of 1g tin dope,
Ultrasonic disperse 30min, is stirred for 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol, then in thermostatic drying chamber in
60 DEG C of dry 5h prepare the bismuth oxychloride/graphene composite photocatalyst containing 0.25wt% tin dope.This composite photo-catalyst exists
Under natural sunlight, the RhB clearance of degraded rhdamine B waste water 3h is 99.91%.
Embodiment 5
By 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;Will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;Under stirring, solution X is dropwise instilled in solution Y, continue stirring 30min, be the hydrogen of 2mol/L by molar concentration
The pH value of sodium hydroxide solution regulation mixed solution is 6, continues stirring 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol,
Then in thermostatic drying chamber, the bismuth oxychloride visible light catalyst of tin dope is prepared in 60 DEG C of dry 5h;By 5mg graphite oxide
The alkene ultrasonic 50mL of being dissolved in water obtains the aqueous solution of Graphene, adds the bismuth oxychloride visible light catalyst of 1g tin dope, super
Sound dispersion 30min, is stirred for 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol, then in 60 in thermostatic drying chamber
DEG C dry 5h prepares the bismuth oxychloride/graphene composite photocatalyst containing 0.5wt% tin dope.This composite photo-catalyst is certainly
So under sunlight, the RhB clearance of degraded rhdamine B waste water 3h is 93.53%.
Embodiment 6
By 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;Will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;Under stirring, solution X is dropwise instilled in solution Y, continue stirring 30min, be the hydrogen of 2mol/L by molar concentration
The pH value of sodium hydroxide solution regulation mixed solution is 6, continues stirring 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol,
Then in thermostatic drying chamber, the bismuth oxychloride visible light catalyst of tin dope is prepared in 60 DEG C of dry 5h;By 10mg graphite oxide
The alkene ultrasonic 50mL of being dissolved in water obtains the aqueous solution of Graphene, adds the bismuth oxychloride visible light catalyst of 1g tin dope, super
Sound dispersion 30min, is stirred for 2h, and sucking filtration is precipitated thing, respectively washes three times with water and ethanol, then in 60 in thermostatic drying chamber
DEG C dry 5h prepares the bismuth oxychloride/graphene composite photocatalyst containing 1wt% tin dope.This composite photo-catalyst is at nature
Under sunlight, the RhB clearance of degraded rhdamine B waste water 3h is 65.23%.
Embodiment above describes the ultimate principle of the present invention, principal character and advantage, the technical staff of the industry should
Understanding, the present invention is not restricted to the described embodiments, and the simply explanation present invention's described in above-described embodiment and description is former
Reason, under the scope without departing from the principle of the invention, the present invention also has various changes and modifications, and these changes and improvements each fall within
In the scope of protection of the invention.
Claims (2)
1. the preparation method of the bismuth oxychloride/graphene composite photocatalyst of a tin dope, it is characterised in that concretely comprise the following steps:
(1) by 1mmol Bi (NO3)3·5H2O is dissolved in obtained solution X in the hydrochloric acid solution that 10mL molar concentration is 1mol/L;(2) will
1mmol SnCl2·2H2O agitating heating is dissolved in that to obtain transparent clarification in the hydrochloric acid solution that 40mL molar concentration is 1mol/L molten
Liquid Y;(3) under stirring, solution X is dropwise instilled in solution Y, be 2mol/L by molar concentration after continuing stirring 30min
Sodium hydroxide solution regulation mixed solution pH value be 6;(4) continue stirring 2h after the pH value of complete mixed solution to be regulated, take out
Filter is precipitated thing, respectively washes three times with water and ethanol, then prepares the chlorine of tin dope in thermostatic drying chamber in 60 DEG C of dry 5h
Bismuth oxide visible light catalyst;(5) ultrasonic for the 0.625-5mg graphene oxide 50mL of being dissolved in water will obtain the water-soluble of Graphene
Liquid, adds the bismuth oxychloride visible light catalyst of 1g tin dope, ultrasonic disperse 30min, is stirred for 2h, and sucking filtration is precipitated
Thing, respectively washes three times with water and ethanol, then prepares the bismuth oxychloride/graphite of tin dope in thermostatic drying chamber in 60 DEG C of dry 5h
Alkene composite photo-catalyst.
The preparation method of the bismuth oxychloride/graphene composite photocatalyst of tin dope the most according to claim 1, its feature
It is: in step (5), the addition of graphene oxide is preferably 2.5mg, the bismuth oxychloride/stone of the tin dope prepared under the conditions of being somebody's turn to do
Ink alkene composite photo-catalyst rhodamine B clearance of degraded rhdamine B waste water 3h under natural sunlight is 99.91%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610663248.5A CN106256430B (en) | 2016-08-15 | 2016-08-15 | A kind of bismuth oxychloride/graphene composite photocatalyst preparation method of tin dope |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610663248.5A CN106256430B (en) | 2016-08-15 | 2016-08-15 | A kind of bismuth oxychloride/graphene composite photocatalyst preparation method of tin dope |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106256430A true CN106256430A (en) | 2016-12-28 |
CN106256430B CN106256430B (en) | 2018-12-21 |
Family
ID=57713683
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610663248.5A Active CN106256430B (en) | 2016-08-15 | 2016-08-15 | A kind of bismuth oxychloride/graphene composite photocatalyst preparation method of tin dope |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106256430B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108359272A (en) * | 2018-03-20 | 2018-08-03 | 常州大学 | It is a kind of using graphene as the preparation method and application of the conductive pearl powder of base material |
CN113318759A (en) * | 2021-05-08 | 2021-08-31 | 华能(广东)能源开发有限公司海门电厂 | Dopamine-mediated bismuth oxychloride photocatalyst and preparation method and application thereof |
CN114768838B (en) * | 2022-04-25 | 2023-07-21 | 长沙学院 | Preparation method and application of Fe-doped BiOCl@Fe-BiOCl core-shell structure nanosheets |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104001495A (en) * | 2014-06-06 | 2014-08-27 | 河南师范大学 | Preparation method of bismuth oxychloride/graphene composite visible light catalyst |
CN104646037A (en) * | 2015-01-12 | 2015-05-27 | 内蒙古科技大学 | BiOXs pholocatalyst, grapheme-compounded BiOXs pholocatalyst and preparation method thereof |
CN105478149A (en) * | 2015-12-02 | 2016-04-13 | 河南师范大学 | Preparation method of tin-doped bismuth oxychloride visible light photocatalyst |
-
2016
- 2016-08-15 CN CN201610663248.5A patent/CN106256430B/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104001495A (en) * | 2014-06-06 | 2014-08-27 | 河南师范大学 | Preparation method of bismuth oxychloride/graphene composite visible light catalyst |
CN104646037A (en) * | 2015-01-12 | 2015-05-27 | 内蒙古科技大学 | BiOXs pholocatalyst, grapheme-compounded BiOXs pholocatalyst and preparation method thereof |
CN105478149A (en) * | 2015-12-02 | 2016-04-13 | 河南师范大学 | Preparation method of tin-doped bismuth oxychloride visible light photocatalyst |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108359272A (en) * | 2018-03-20 | 2018-08-03 | 常州大学 | It is a kind of using graphene as the preparation method and application of the conductive pearl powder of base material |
CN108359272B (en) * | 2018-03-20 | 2020-06-16 | 常州大学 | Preparation method and application of conductive pearl powder with graphene as base material |
CN113318759A (en) * | 2021-05-08 | 2021-08-31 | 华能(广东)能源开发有限公司海门电厂 | Dopamine-mediated bismuth oxychloride photocatalyst and preparation method and application thereof |
CN113318759B (en) * | 2021-05-08 | 2023-09-05 | 华能(广东)能源开发有限公司海门电厂 | Dopamine-mediated bismuth oxychloride photocatalyst, and preparation method and application thereof |
CN114768838B (en) * | 2022-04-25 | 2023-07-21 | 长沙学院 | Preparation method and application of Fe-doped BiOCl@Fe-BiOCl core-shell structure nanosheets |
Also Published As
Publication number | Publication date |
---|---|
CN106256430B (en) | 2018-12-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Habib et al. | Synthesis and characterization of ZnO-TiO 2 nanocomposites and their application as photocatalysts | |
Ilinoiu et al. | Photocatalytic activity of a nitrogen-doped TiO2 modified zeolite in the degradation of Reactive Yellow 125 azo dye | |
CN104525226B (en) | A kind of photocatalyst Bi4o5br2synthesis and application process | |
CN106824246B (en) | A kind of TiO2/g-C3N4The preparation method of composite visible light catalyst | |
CN101254463B (en) | Synthetic method of visible light catalyst Bi2MoO6 | |
CN102335602B (en) | Bismuth tungstate composite photocatalyst, preparation method thereof, and application thereof | |
Samsudin et al. | Photocatalytic degradation of real industrial poultry wastewater via platinum decorated BiVO4/g-C3N4 photocatalyst under solar light irradiation | |
Zangeneh et al. | N (Urea) and CN (L-Asparagine) doped TiO2-CuO nanocomposites: fabrication, characterization and photodegradation of direct red 16 | |
CN104998665A (en) | Preparation method and application of BiVO4-BiOBr photocatalyst | |
CN105536819B (en) | A kind of preparation method of graphene/antimony trisulfide composite photo-catalyst | |
CN108927176B (en) | Copper sulfide/bismuth vanadate heterojunction photocatalyst and preparation method thereof | |
CN103191725B (en) | BiVO4/Bi2WO6 composite semiconductor material as well as hydrothermal preparation method and application thereof | |
CN104475131B (en) | Visible light response type nanosheet bismuth oxychloride catalyst and preparation method thereof | |
CN105435847B (en) | A kind of Bi2WO6/ BiOI@quaternary ammonium salts are inorganic/organic composite photo-catalyst agent and preparation method thereof | |
CN106256430B (en) | A kind of bismuth oxychloride/graphene composite photocatalyst preparation method of tin dope | |
Alshaikh et al. | Promoted visible-light photocatalytic reduction of Hg2+ over CuAl2O4-decorated g-C3N4 nanoheterojunctions synthesized by solution process | |
CN109158124A (en) | A kind of carbonitride and BiOX composite photocatalyst material and preparation method thereof | |
CN102357360A (en) | Catalyst for degrading rhodamine B by photocatalysis, and preparation method thereof | |
Van Thuan et al. | Photodegradation of hazardous organic pollutants using titanium oxides-based photocatalytic: A review | |
CN102600865A (en) | Photocatalyst for degrading organic dye waste water pollutants and preparation method thereof | |
Kumaravel et al. | Fabrication of Ag/WO3/g-C3N4 composites for the photocatalytic degradation of harmful dyes | |
CN103721713B (en) | A kind of three-phase composite visible of efficient degradation dyestuff | |
CN108144599A (en) | A kind for the treatment of process of bismuthino composite photocatalyst for degrading dyeing waste water | |
CN104016515A (en) | Method for treating printing and dyeing wastewater by photocatalytic oxidation | |
CN105498750A (en) | Preparation method of bismuth tungstate/graphene photocatalyst with broad-spectrum degradation property |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |