CN113042079A - Modified N, S-GQDs @ CdS nano-catalyst and preparation and application thereof - Google Patents
Modified N, S-GQDs @ CdS nano-catalyst and preparation and application thereof Download PDFInfo
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- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
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- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01J35/00—Catalysts, in general, characterised by their form or physical properties
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- B01J35/39—Photocatalytic properties
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- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
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Abstract
The invention relates to a modified N, S-GQDs @ CdS nano catalyst, and preparation and application thereof. The preparation method specifically comprises the following steps: (a) dissolving citric acid and thiourea in water, performing ultrasonic dispersion, transferring to a reactor for hydrothermal reaction, and sequentially cooling, rotary steaming and drying to obtain N, S-GQDs; (b) dissolving the N, S-GQDs obtained in the step (a) in water, adding cadmium acetate dihydrate, polyvinylpyrrolidone and thioacetamide, mixing, performing ultrasonic dispersion, transferring to a reactor for hydrothermal reaction, and then sequentially cooling, washing and drying to obtain the N, S-GQDs @ CdS. Compared with the prior art, the photocatalyst can expand the light absorption range, is beneficial to hole-electron separation, can improve the catalytic efficiency, and has good degradation capability on methylene blue under the condition of ultraviolet light.
Description
Technical Field
The invention belongs to the technical field of photocatalysis, and particularly relates to a modified N, S-GQDs @ CdS nano-catalyst, and preparation and application thereof.
Background
The catalyst was first discovered by the swedish chemist bei elli usa and has been known for over 100 years. The catalyst has a plurality of types and has important and wide application in chemical production. Wherein the photocatalyst is prepared by Fujishima in 1972 by irradiating with TiO under ultraviolet light2The discovery of water degradation has brought about a hot tide in semiconductor photocatalyst research, and the photocatalytic elimination and degradation of pollutants are an active research direction at present. The semiconductor photocatalyst is TiO2Silver-based semiconductors, tungsten-based semiconductors, ZnO, CdS and other semiconductor materials as a general term of substances for photocatalytic degradation. The photocatalyst mainly utilizes the fact that the energy of the emission of sunlight and ultraviolet light is larger than the energy gap of a semiconductor material, and valence band electrons in the semiconductor are excited to jump to a high-energy conduction band during illumination, so that electrons and holes are left in the valence band, and a part of photogenerated electrons (e) are generated-) And a cavity (h)+) The photocatalyst is diffused to the surface of the photocatalyst and finally has oxidation-reduction reaction with electrons or electron acceptors adsorbed on the surface of the photocatalyst, so that a series of chemical reactions initiated by active groups of the photocatalyst are formed, and the photocatalyst has the advantages of proper energy band potential, high chemical stability, no toxicity, no harm, higher photoelectric conversion efficiency, low cost, high activity and the like, so that the photocatalyst becomes an irreplaceable preferred material in chemical production and is mainly applied to the fields of organic synthesis, catalytic chemistry, environmental management, electrochemistry, biochemistry and the like.
However, the conventional photocatalyst is generally a single photocatalyst, and photo-generated electrons and holes generated in the process of illumination are easily self-recombined, which can reduce the number of the photo-generated electrons and holes, further cause the loss of active sites on the surface of the catalyst, reduce the photocatalytic efficiency, and hinder the further development of the photocatalyst. The modified graphene quantum dots integrate quantum confinement, size effect and edge effect, have the advantages of good water solubility, low biotoxicity, excellent chemical inertness, stable fluorescence, easy surface modification performance, excellent luminescence performance, adjustable band gap and the like, and have wide application prospects in the fields of chemical sensing, biological imaging, medical treatment and energy correlation. Therefore, it is imperative to modify the traditional photocatalyst to prepare a high-efficiency photocatalyst, and how to improve the effective active sites by the mutual combination of the modified photocatalyst or multiple photocatalysts, reduce the recombination rate of the photogenerated electrons and holes generated in the illumination process, and improve the photocatalytic efficiency has become a hotspot of research at present.
Disclosure of Invention
The invention aims to provide a modified N, S-GQDs @ CdS nano catalyst, and preparation and application thereof.
The purpose of the invention is realized by the following technical scheme:
a modified N, S-GQDs @ CdS nano catalyst takes CdS as a core, N, S-GQDs grow on the surface, namely cadmium sulfide is the core, the N, S-GQDs are loaded on the surface of the CdS, the particle size of the N, S-GQDs is 2-7nm, the particle size of the CdS is 700-905nm, the CdS and the core are connected through a covalent bond, wherein the GQDs represent Graphene quantum dots (Graphene quantum dots), the N, S-GQDs refer to the Graphene quantum dots doped by nitrogen elements and sulfur elements, the specific surface area of the spherical CdS is greatly increased, the transmission rate of photogenerated electrons and holes on the surface of the cadmium sulfide is increased during illumination, and the photocatalysis efficiency is increased.
The preparation method of the modified N, S-GQDs @ CdS nano-catalyst specifically comprises the following steps:
(a) dissolving citric acid and thiourea in water, performing ultrasonic dispersion, transferring to a reactor for hydrothermal reaction, sequentially cooling, performing rotary evaporation and drying to obtain N, S-GQDs, and emitting blue fluorescence at 365 nm;
(b) dissolving the N, S-GQDs obtained in the step (a) in water, adding cadmium acetate dihydrate, polyvinylpyrrolidone (PVP for short) and thioacetamide, mixing, ultrasonically dispersing, transferring to a reactor for hydrothermal reaction, and then sequentially cooling, washing and drying to obtain the N, S-GQDs @ CdS, wherein the polyvinylpyrrolidone plays a role of a cross-linking agent to enable the N, S-GQDs to be better loaded on the cadmium sulfide, and the cadmium acetate dihydrate and the thioacetamide react to obtain the CdS.
In the step (a), the molar ratio of citric acid to thiourea is 1:3, and the N, S-GQDs quantum dot generated in the ratio has the best structural effect and uniform particle size and can be uniformly dispersed on CdS.
In the step (a), the power of the ultrasonic wave is 150W, and the time of the ultrasonic wave is 0.1h, so that the reaction raw materials are uniformly dispersed to fully react.
In the step (a), the temperature of the hydrothermal reaction is 160-200 ℃, preferably 180 ℃, and the time is 4-8h, preferably 6 h.
In the step (b), the mass ratio of N, S-GQDs, cadmium acetate dihydrate, polyvinylpyrrolidone and thioacetamide is (0.02-0.06):0.266:0.2: (0.0.751-0.1503), preferably 0.04:0.266:0.2: 0.1127.
In step (b), Cd in cadmium acetate dihydrate2+And S in thioacetamide2-The molar ratio of (1) to (2).
In step (b), Cd in cadmium acetate dihydrate2+And S in thioacetamide2-Preferably in a molar ratio of 1: 1.5.
In the step (b), the power of the ultrasonic wave is 150W, and the time of the ultrasonic wave is 0.5h, so that the reaction raw materials are uniformly dispersed to fully react.
In the step (b), the temperature of the hydrothermal reaction is 160-200 ℃, preferably 180 ℃, and the time is 6-18h, preferably 12 h.
In step (b), cooling to room temperature, washing with anhydrous ethanol, and drying at 60 deg.C overnight
The application of the N, S-GQDs @ CdS nano-catalyst in degrading dye wastewater is described. Under the irradiation of ultraviolet light, the degradation effect of N, S-GQDs @ CdS on methylene blue is very excellent.
The invention provides a N, S-GQDs @ CdS nano catalyst, and the performance of the catalyst is regulated and controlled by controlling the reaction time of hydrothermal reaction, the using amount of a precursor N, S-GQDs and the using amount of sodium thioacetamide, so that the N, S-GQDs can be stably loaded on the surface of CdS under a proper condition, and finally the N, S-GQDs @ CdS catalyst is obtained, and the N, S-GQDs in the catalyst can emit blue fluorescence under 365 nm. The introduction of N, S-GQDs into the CdS surface of the carrier can enlarge the light absorption range, is beneficial to the separation of holes and electrons, and can also improve the catalytic efficiency, and has good degradation capability on methylene blue under the ultraviolet condition. Compared with the traditional single N, S-GQDs and CdS, the N, S-GQDs @ CdS nano-catalyst obtained by the method overcomes the problems of instability of the single catalyst, photo-generated electron and hole recombination and self-optical defects of the CdS, remarkably improves the catalytic efficiency, and expands the application of the N, S-GQDs @ CdS nano-catalyst in the aspect of photocatalytic degradation of dye wastewater. According to the invention, through selecting other conditions such as used raw materials, temperature and the like, the obtained final product is used for degrading methylene blue pollutants under a certain illumination condition, and the difference of the treatment effects of different catalysts prepared under different material doping conditions on the pollutants is explored, so that more ideas are provided for degrading dye wastewater.
Drawings
FIG. 1 is an infrared spectrum of the N, S-GQDs @ CdS nanocatalyst of example 1;
FIG. 2 is a Raman spectrum of the N, S-GQDs @ CdS nanocatalyst of example 1;
FIG. 3 is an SEM electron micrograph of the N, S-GQDs @ CdS nanocatalyst of example 1;
FIG. 4 is a graph showing the substantial comparison between the non-fluorescence of N, S-GQDs under natural light irradiation and the blue fluorescence under 365nm light irradiation in example 1;
FIG. 5 is a graph of the efficiency of N, S-GQDs @ CdS nanocatalyst degrading methylene blue as a function of time and light conditions in example 2;
FIG. 6 is a graph showing the efficiency of degrading methylene blue by N, S-GQDs nanocatalyst in comparative example 1 as a function of time and illumination conditions;
fig. 7 is a graph showing the efficiency of the CdS nanocatalyst degrading methylene blue in comparative example 2 as a function of time and illumination conditions.
Detailed Description
The invention is described in detail below with reference to the figures and specific embodiments.
The raw materials used in the invention can be purchased in the market, are all analytically pure, do not need further treatment and can be directly used, wherein the citric acid, the thiourea, the cadmium acetate dihydrate, the polyvinylpyrrolidone and the thioacetamide are all purchased from chemical reagents of national drug group, Inc.
Example 1
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, wherein the raw materials comprise citric acid, thiourea, cadmium acetate dihydrate, polyvinylpyrrolidone and thioacetamide, and 0.21g of citric acid, 0.2283g of thiourea, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.1127g of thioacetamide are added. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing for 0.1h at 150W, transferring the solution into a 50mL hydrothermal reaction kettle, placing the reaction kettle into a drying box, preserving heat at 180 ℃ for 6h, cooling, performing rotary evaporation and drying (according to the experimental parameters and experimental operation steps commonly used in laboratories, the same applies below) to prepare N, S-GQDs, placing the N, S-GQDs under natural light for irradiation, wherein the compound does not fluoresce, as shown in the left graph in FIG. 4, placing the N, S-GQDs under 365nm for irradiation, and the compound fluoresces blue, as shown in the right graph in FIG. 4;
(2) 20mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.1127g of thioacetamide (Cd)2+: S2-1:1.5), ultrasonically dispersing for 0.5h at the power of 150W, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the temperature for 12h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying at 60 ℃ overnight to prepare N, S-GQDs @ CdS. The infrared spectrogram and the Raman spectrogram of the catalyst are respectively shown in fig. 1 and 2, in the infrared spectrogram, a characteristic peak 1590C-N double bond and a characteristic peak 1200C-C single bond indicate that nitrogen elements are successfully doped into graphene quantum dots, a characteristic peak 1590C-S bond indicates that the nitrogen-doped graphene quantum dots and cadmium sulfide are connected by a C-S covalent bond, and an electron microscope picture of the catalyst is shown in fig. 3, so that CdS particles are full and substantially spherical, and the particle size is 789-905 nm.
The catalyst is used for catalyzing methylene blue, and specifically comprises the following components: putting 50mgN, S-GQDs @ CdS nano-catalyst into a 150mL quartz tube, adding 10mg/L methylene blue solution into the quartz tube, adding a rotor into the quartz tube, opening a photocatalytic reactor, stirring for 90min under dark conditions to achieve adsorption-desorption balance, then opening a water circulation system, carrying out photocatalytic degradation under the condition of 500w xenon lamp, taking samples every 10min, filtering by using a 0.22 mu m microporous filter head to remove residual catalyst, and then measuring absorbance in an ultraviolet spectrophotometer (the same below). The degradation efficiency calculation formula is as follows: eta is At/A0Eta: degradation efficiency; a. thet: absorbance at a certain time: a. the0: initial absorbance (same below). The degradation efficiency and the photocatalytic efficiency are shown in table 1, and the degradation efficiency of the N, S-GQDs @ CdS nano-catalyst to methylene blue under the ultraviolet light condition can be known as follows: when the amount of N, S-GQDs is insufficient, the N, S-GQDs loaded on the surface of CdS are insufficient to provide more effective active sites, so that the efficiency of degrading methylene blue is not high.
Example 2
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, and the raw materials comprise 0.21g of citric acid, 0.2283g of thiourea, 40mg of N, S-GQDs, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.1127g of thioacetamide. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing for 0.1h at 150W, transferring into a 50mL hydrothermal reaction kettle, putting the reaction kettle into a drying box, preserving heat for 6h at 180 ℃, cooling, rotary steaming and drying to prepare N, S-GQDs;
(2) 40mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.1127g of thioacetamide (Cd)2+:S2-1:1.5), ultrasonically dispersing for 0.5h at the power of 150W, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the heat for 12h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying overnight at 60 ℃ to prepare N, S-GQDs @ CdS.
When the catalyst is used for catalyzing methylene blue, the degradation efficiency and the photocatalytic efficiency are specifically shown in table 1, the change situation of the degradation efficiency along with time is shown in fig. 5, and the degradation efficiency of the N, S-GQDs @ CdS nano-catalyst to the methylene blue under the ultraviolet light condition can be known as follows: when the N, S-GQDs are proper, the N, S-GQDs loaded on the surface of CdS can provide enough effective active sites, so that the efficiency of degrading methylene blue is the best.
Example 3
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, and the raw materials comprise 0.21g of citric acid, 0.2283g of thiourea, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.1127g of thioacetamide. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing for 0.1h at 150W, transferring into a 50mL hydrothermal reaction kettle, putting the reaction kettle into a drying box, preserving heat for 6h at 180 ℃, cooling, rotary steaming and drying to prepare N, S-GQDs;
(2) 60mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.1127g of thioacetyl (Cd, g)2+: S2-1:1.5), ultrasonically dispersing for 0.5h at the power of 150W, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the heat for 12h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying overnight at 60 ℃ to prepare N, S-GQDs @ CdS.
When the catalyst is used for catalyzing methylene blue, the degradation efficiency and the photocatalytic efficiency are specifically shown in table 1, and the degradation efficiency of the N, S-GQDs @ CdS nano catalyst to the methylene blue under the ultraviolet light condition can be known as follows: when the amount of N, S-GQDs is excessive, agglomeration can be generated, and the N, S-GQDs loaded on the surface of CdS are not enough to provide more effective active sites, so that the efficiency of degrading methylene blue is not high.
Example 4
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, and the raw materials comprise 0.21g of citric acid, 0.2283g of thiourea, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.1127g of thioacetamide. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing for 0.1h at 150W, transferring into a 50mL hydrothermal reaction kettle, putting the reaction kettle into a drying box, preserving heat for 6h at 180 ℃, cooling, rotary steaming and drying to prepare N, S-GQDs;
(2) 40mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.1127g of sulfurAcetyl (Cd)2+: S2-1:1.5), ultrasonically dispersing for 0.5h at the power of 150W, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the heat for 6h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying overnight at 60 ℃ to prepare N, S-GQDs @ CdS.
When the catalyst is used for catalyzing methylene blue, the degradation efficiency and the photocatalytic efficiency are specifically shown in table 1, and the degradation efficiency of the N, S-GQDs @ CdS nano catalyst to the methylene blue under the ultraviolet light condition can be known as follows: when the hydrothermal reaction time is insufficient, the anchoring of N, S-GQDs on the surface of the CdS carrier is unstable, and more effective active sites are not sufficiently provided, so that the efficiency of degrading methylene blue is not high.
Example 5
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, and the raw materials comprise 0.21g of citric acid, 0.2283g of thiourea, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.1127g of thioacetamide. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing for 0.1h at 150W, transferring into a 50mL hydrothermal reaction kettle, putting the reaction kettle into a drying box, preserving heat for 6h at 180 ℃, cooling, rotary steaming and drying to prepare N, S-GQDs;
(2) 40mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.1127g of thioacetyl (Cd, g)2+: S2-1:1.5), ultrasonically dispersing for 0.5h at the power of 150W, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the heat for 18h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying overnight at 60 ℃ to prepare N, S-GQDs @ CdS.
When the catalyst is used for catalyzing methylene blue, the degradation efficiency and the photocatalytic efficiency are specifically shown in table 1, and the degradation efficiency of the N, S-GQDs @ CdS nano catalyst to the methylene blue under the ultraviolet light condition can be known as follows: when the hydrothermal reaction time is too long, the N, S-GQDs are agglomerated on the surface of the CdS carrier, and are not enough to provide more effective active sites, so that the efficiency of degrading methylene blue is not high.
Example 6
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, and the raw materials comprise 0.21g of citric acid, 0.2283g of thiourea, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.0751g of thioacetamide. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing for 0.1h at 150W, transferring into a 50mL hydrothermal reaction kettle, putting the reaction kettle into a drying box, preserving heat for 6h at 180 ℃, cooling, rotary steaming and drying to prepare N, S-GQDs;
(2) 40mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.0751g of thioacetyl (Cd, N-acetyl-D) in2+: S2-1:1), ultrasonically dispersing for 0.5h at the power of 150W, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the heat for 12h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying overnight at 60 ℃ to prepare N, S-GQDs @ CdS.
When the catalyst is used for catalyzing methylene blue, the degradation efficiency and the photocatalytic efficiency are specifically shown in table 1, and the degradation efficiency of the N, S-GQDs @ CdS nano catalyst to the methylene blue under the ultraviolet light condition can be known as follows: when Cd2+: S2-At 1:1, the binding of N, S-GQDs to the CdS carrier is not complete and insufficient to provide more effective active sites, and thus is not efficient for methylene blue degradation.
Example 7
The catalyst takes CdS as a core, the particle size of N, S-GQDs growing on the surface of the catalyst is 2-7nm, the CdS is spherical, the particle size of the CdS is 700-905nm, and the N, S-GQDs growing on the surface of the catalyst and the CdS are connected through a covalent bond. The compound is prepared by the following preparation method, and the raw materials comprise 0.21g of citric acid, 0.2283g of thiourea, 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone and 0.1503g of thioacetamide. The method comprises the following specific steps:
(1) weighing 0.21g of citric acid and 0.2283g of thiourea, dissolving in 40mL of deionized water, ultrasonically dispersing, transferring into a 50mL hydrothermal reaction kettle, putting the reaction kettle into a drying box, keeping the temperature at 180 ℃ for 6h, cooling, rotary steaming and drying to prepare N, S-GQDs;
(2) 40mg of the N, S-GQDs prepared above was placed in a 80mL beaker containing deionized water, to which was added 0.266g of cadmium acetate dihydrate, 0.2g of polyvinylpyrrolidone, and 0.1503g of thioacetyl (Cd, g)2+: S2-1:2), ultrasonically dispersing, transferring the mixture into a 100mL hydrothermal reaction kettle, preserving the temperature for 12h at 180 ℃, cooling to room temperature, washing with absolute ethyl alcohol, and drying overnight at 60 ℃ to prepare N, S-GQDs @ CdS.
When the catalyst is used for catalyzing methylene blue, the degradation efficiency and the photocatalytic efficiency are shown in table 1, and the degradation efficiency of the N, S-GQDs @ CdS nano-catalyst to the methylene blue under the ultraviolet light condition can be known as follows: when Cd2+:S2-When the ratio is 1:2, the CdS carrier is agglomerated, N, S-GQDs cannot be completely loaded on CdS and cannot provide more effective active sites, so that the efficiency of degrading methylene blue is not high.
TABLE 1 summary of the efficiency of degrading methylene blue of N, S-GQDs nanocatalysts prepared in each example and two comparative examples
In conclusion, when the molar ratio of the citric acid to the thiourea is 1:3, the mass ratio of the N, S-GQDs, the cadmium acetate dihydrate, the polyvinylpyrrolidone and the thioacetamide is 0.04:0.266:0.2:0.1127, and the Cd is2+And S2-The molar ratio of the N to the S-GQDs @ CdS nano-catalyst is 1:1.5, the reaction temperature of the hydrothermal reaction in the step (2) is 180 ℃, and the reaction time is 12 hours, so that the prepared N, S-GQDs @ CdS nano-catalyst has the optimal degradation performance, and the effect of degrading methylene blue with the concentration of 10mg/L is very excellentThe degradation efficiency can reach 100% when the catalyst is irradiated for 90min under the illumination condition, and the degradation efficiency of the catalyst prepared under other conditions is more than 76% under the illumination condition, and is basically superior to the catalytic effect of a single N, S-GQDs catalyst and a single CdS catalyst.
Comparative example 1
50mg of N, S-GQDs catalyst (obtained by the preparation step (1) shown in example 2) was placed in a 150mL quartz tube, 10mg/L of methylene blue solution was added to the quartz tube, a rotor was added to the quartz tube, a photocatalytic reactor was opened, and stirred under dark conditions for 90min to achieve adsorption-desorption equilibrium, at this time, a water circulation system was opened, photocatalytic degradation was performed under a 500w xenon lamp, samples were taken every 10min, and filtered with a 0.22 μm microporous filter to remove the residual catalyst, and then absorbance measurement was performed in an ultraviolet spectrophotometer, specifically as shown in FIG. 6, the degradation efficiency was 19% for 90min under dark conditions, and the degradation efficiency was 63% for 90min under light conditions.
Comparative example 2
50mg of CdS catalyst (obtained by the same operation as in the preparation step (2) shown in example 2 except that N, S-GQDs and polyvinylpyrrolidone were not added to the CdS catalyst) was placed in a 150mL quartz tube, 10mg/L of methylene blue solution was added to the quartz tube, a rotor was added to the quartz tube, the photocatalytic reactor was opened, stirring in dark for 90min to reach adsorption-desorption balance, opening water circulation system, performing photocatalytic degradation under 500w xenon lamp, sampling every 10min, filtering with 0.22 μm microporous filter head to remove residual catalyst, measuring absorbance in ultraviolet spectrophotometer, specifically shown in FIG. 7, the degradation efficiency is 23% in 90min under dark condition and 78% in 90min under illumination condition.
Example 8
A modified N, S-GQDs @ CdS nano-catalyst is prepared by the following preparation method, except that the hydrothermal temperature in the step (1) is 160 ℃ and the time is 8 hours, the hydrothermal temperature in the step (2) is 160 ℃ and the time is 18 hours, and the rest is the same as the preparation steps of the example 2.
Example 9
A modified N, S-GQDs @ CdS nano-catalyst is prepared by the following preparation method, except that the hydrothermal temperature in the step (1) is 200 ℃ and the time is 4 hours, the hydrothermal temperature in the step (2) is 200 ℃ and the time is 8 hours, and the rest steps are the same as the preparation steps of the example 2.
The embodiments described above are described to facilitate an understanding and use of the invention by those skilled in the art. It will be readily apparent to those skilled in the art that various modifications to these embodiments may be made, and the generic principles described herein may be applied to other embodiments without the use of the inventive faculty. Therefore, the present invention is not limited to the above embodiments, and those skilled in the art should make improvements and modifications within the scope of the present invention based on the disclosure of the present invention.
Claims (10)
1. The modified N, S-GQDs @ CdS nano-catalyst is characterized in that the catalyst takes CdS as a core, N, S-GQDs grow on the surface of the CdS as the core, the N, S-GQDs are connected through covalent bonds, and the N, S-GQDs are graphene quantum dots doped with nitrogen elements and sulfur elements.
2. The preparation method of the modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 1, wherein the preparation method specifically comprises the following steps:
(a) dissolving citric acid and thiourea in water, performing ultrasonic dispersion, transferring to a reactor for hydrothermal reaction, and sequentially cooling, rotary steaming and drying to obtain N, S-GQDs;
(b) dissolving the N, S-GQDs obtained in the step (a) in water, adding cadmium acetate dihydrate, polyvinylpyrrolidone and thioacetamide, mixing, performing ultrasonic dispersion, transferring to a reactor for hydrothermal reaction, and then sequentially cooling, washing and drying to obtain the N, S-GQDs @ CdS.
3. The method for preparing the modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 2, wherein in step (a), the molar ratio of citric acid to thiourea is 1: 3.
4. The method for preparing the modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 2, wherein in the step (a), the temperature of the hydrothermal reaction is 160-200 ℃ and the time is 4-8 h.
5. The preparation method of the modified N, S-GQDs @ CdS nano-catalyst as claimed in claim 2, wherein in step (b), the mass ratio of N, S-GQDs, cadmium acetate dihydrate, polyvinylpyrrolidone and thioacetamide is (0.02-0.06):0.266:0.2 (0.0.751-0.1503).
6. The method for preparing a modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 2, wherein in step (b), Cd in cadmium acetate dihydrate2+And S in thioacetamide2-The molar ratio of (1) to (2).
7. The method for preparing a modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 2, wherein in step (b), Cd in cadmium acetate dihydrate2+And S in thioacetamide2-In a molar ratio of 1: 1.5.
8. The method for preparing the modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 2, wherein in the step (b), the temperature of the hydrothermal reaction is 160-200 ℃ and the time is 6-18 h.
9. The method for preparing a modified N, S-GQDs @ CdS nanocatalyst as claimed in claim 2, wherein in step (b), cooling to room temperature, washing with absolute ethanol, and drying at 60 ℃ overnight.
10. The use of the N, S-GQDs @ CdS nanocatalyst as defined in claim 1 for degrading dye wastewater.
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