CN106268865A - A kind of cadmium sulfide C-base composte material is as the preparation method of photoelectric - Google Patents
A kind of cadmium sulfide C-base composte material is as the preparation method of photoelectric Download PDFInfo
- Publication number
- CN106268865A CN106268865A CN201610566303.9A CN201610566303A CN106268865A CN 106268865 A CN106268865 A CN 106268865A CN 201610566303 A CN201610566303 A CN 201610566303A CN 106268865 A CN106268865 A CN 106268865A
- Authority
- CN
- China
- Prior art keywords
- carrageenan
- gel
- cadmium
- photoelectric
- cadmium sulfide
- 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
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 title claims abstract description 35
- 229910052980 cadmium sulfide Inorganic materials 0.000 title claims abstract description 35
- 239000000463 material Substances 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims abstract description 20
- 229920001525 carrageenan Polymers 0.000 claims abstract description 29
- 229940113118 carrageenan Drugs 0.000 claims abstract description 29
- 239000000679 carrageenan Substances 0.000 claims abstract description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 21
- 235000010418 carrageenan Nutrition 0.000 claims abstract description 20
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims abstract description 20
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 12
- 230000008569 process Effects 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 7
- 239000002994 raw material Substances 0.000 claims abstract description 7
- 239000001569 carbon dioxide Substances 0.000 claims abstract description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims abstract description 6
- 238000003763 carbonization Methods 0.000 claims abstract description 6
- 239000002131 composite material Substances 0.000 claims abstract description 6
- QWCAGKZBJUCBEI-UHFFFAOYSA-N [C+4].[S-2].[Cd+2].[S-2].[S-2] Chemical compound [C+4].[S-2].[Cd+2].[S-2].[S-2] QWCAGKZBJUCBEI-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052724 xenon Inorganic materials 0.000 claims abstract description 5
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 230000029087 digestion Effects 0.000 claims abstract description 4
- 238000012545 processing Methods 0.000 claims abstract description 4
- 238000012360 testing method Methods 0.000 claims abstract description 4
- GHKPAWKFKPJNSC-UHFFFAOYSA-L C(C)O.C(C)(=O)[O-].[Cd+2].C(C)(=O)[O-] Chemical compound C(C)O.C(C)(=O)[O-].[Cd+2].C(C)(=O)[O-] GHKPAWKFKPJNSC-UHFFFAOYSA-L 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 5
- LHQLJMJLROMYRN-UHFFFAOYSA-L cadmium acetate Chemical compound [Cd+2].CC([O-])=O.CC([O-])=O LHQLJMJLROMYRN-UHFFFAOYSA-L 0.000 claims description 3
- 208000011580 syndromic disease Diseases 0.000 claims description 3
- 238000007710 freezing Methods 0.000 claims description 2
- 230000008014 freezing Effects 0.000 claims description 2
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 2
- 238000001354 calcination Methods 0.000 abstract description 2
- 238000004108 freeze drying Methods 0.000 abstract description 2
- 229910052793 cadmium Inorganic materials 0.000 abstract 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 2
- 230000001699 photocatalysis Effects 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000206572 Rhodophyta Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229930182830 galactose Natural products 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000007146 photocatalysis Methods 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 241000195474 Sargassum Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XCXQDNJHSAGIJC-UHFFFAOYSA-N [C].[Cd] Chemical compound [C].[Cd] XCXQDNJHSAGIJC-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 description 1
- KJNYWDYNPPTGLP-UHFFFAOYSA-L cadmium(2+);diacetate;hydrate Chemical compound O.[Cd+2].CC([O-])=O.CC([O-])=O KJNYWDYNPPTGLP-UHFFFAOYSA-L 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical group [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 239000011941 photocatalyst Substances 0.000 description 1
- -1 polysaccharide compound Chemical class 0.000 description 1
- 150000004804 polysaccharides Polymers 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000005987 sulfurization 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
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/04—Sulfides
-
- 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
- B01J35/33—Electric or magnetic 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
- B01J35/30—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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
- B01J37/082—Decomposition and pyrolysis
-
- 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
- B01J37/32—Freeze drying, i.e. lyophilisation
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Catalysts (AREA)
- Hybrid Cells (AREA)
Abstract
The invention discloses a kind of cadmium sulfide C-base composte material preparation method as photoelectric, preparation process of the present invention is simple, it is not necessary to expensive device, and products obtained therefrom quality high-performance is good.The technical solution used in the present invention is: step one, utilize the gel principle of carrageenan, the carrageenan raw material of high-temperature digestion is instilled in the ethanol solution of hydrochloric acid, forms gel, does gel roguing and process;Step 2, after roguing carrageenan gel immerse certain density cadmium acetate ethanol solution in, repeatedly process;Step 3, above-mentioned gel ethanol and moisture being walked and cleans, the gel after processing is put in refrigerator, and then lyophilization forms cadmium carrageenan aeroge;Step 4, cadmium carrageenan aeroge through certain carbonization technique calcining, high temperature de-carbon in carbon dioxide the most again, obtain cadmium sulfide carbon back composite photoelectric catalyst in tube furnace;Step 5, use electrochemical workstation and xenon lamp systems test the PhotoelectrocatalytiPerformance Performance of above-mentioned product.
Description
Technical field
The invention belongs to photoelectrocatalysis field, particularly relate to a kind of cadmium sulfide C-base composte material as photoelectric
Preparation method.
Background technology
Energy gap under cadmium sulfide (CdS) room temperature is 2.4eV, has excellent visible absorption performance, the taboo that CdS is narrow
Bandwidth and negative conduction band limit make it a kind of promising catalysis material.But, as catalysis material, it has
Not enough: first, light induced electron and hole-recombination are fast, cause it low to sunlight absorption efficiency, secondly, and the light stability of cadmium sulfide
Poor.In the face of these problems, developing a kind of stable cadmium sulfide photocatalyst is significantly.
Carrageenan is the Sargassum macromolecular polysaccharide (as shown in figure a) extracted from red algae.Its chemical constitution is by sulfate
Changing or the galactose of non-sulfuric acid base and 3,6-dehydration inner ether galactose is by α-1, and 3-glycosidic bond and β-Isosorbide-5-Nitrae glycosidic bond alternately connect
The linear polysaccharide compound connect, containing one or two sulfate group, total sulfuric ester in polysaccharide chain in its most sugar units
Base content is 15% ~ 40%.Κ-type and ι-type carrageenan can form heat-convertible gel in aqueous by double-spiral structure,
Its mechanism is as shown in figure b.Cadmium sulfide C-base composte material is obtained finally by high temperature carbonization.
Summary of the invention
The deficiency existed for prior art, the present invention utilizes the carrageenan of abundance as raw material, is prepared for having
Very high visible response and stable cadmium sulfide C-base composte material.
Preparation process of the present invention is simple, it is not necessary to expensive device, and products obtained therefrom quality high-performance is good, at photoelectrocatalysis in future
Field has reliable prospect.
For solving above-mentioned technical problem, the technical solution used in the present invention is: a kind of cadmium sulfide C-base composte material is made
For the preparation method of photoelectric, specifically comprise the following steps that
Step one, utilize the gel principle of carrageenan, the carrageenan raw material of high-temperature digestion is instilled in the ethanol solution of hydrochloric acid, shape
Become gel, do gel roguing and process;
Step 2, after roguing carrageenan gel immerse certain density cadmium acetate ethanol solution in, repeatedly process;
Step 3, above-mentioned gel ethanol and moisture being walked and cleans, the gel after processing is put in refrigerator, then freezing dry
Dry, form cadmium-carrageenan aeroge;
Step 4, cadmium-carrageenan aeroge is calcined through certain carbonization technique in tube furnace, high in carbon dioxide the most again
Temperature de-carbon, obtains cadmium sulfide carbon back composite photoelectric catalyst;
Step 5, use electrochemical workstation and xenon lamp systems test the PhotoelectrocatalytiPerformance Performance of above-mentioned product.
Above-mentioned cadmium sulfide C-base composte material is as the preparation method of photoelectric, the carrageenan in described step one
Mass fraction be 2 %, the ethanol solution concentration of hydrochloric acid is 2mol L-1.
Above-mentioned cadmium sulfide C-base composte material is as the preparation method of photoelectric, the cadmium acetate in described step 2
Substance withdrawl syndrome be 1.5mol L-1, number of processes is 3 ~ 5 times.
Above-mentioned cadmium sulfide C-base composte material as the preparation method of photoelectric, the ethanol in described step 3 and
Moisture other places are managed 2 ~ 3 times.
Above-mentioned cadmium sulfide C-base composte material is as the preparation method of photoelectric, the carbonizer in described step 4
Skill be in nitrogen atmosphere 700 DEG C calcine 1 hour, then 610 DEG C of de-carbons 1 hour in carbon dioxide.
Cadmium sulfide C-base composte material of the present invention as the advantage of the preparation method of photoelectric is: the present invention uses
Raw material is mainly ι-carrageenan, and ι-carrageenan is to extract in red algae, wide material sources, environment-friendly and green, safety height.This
Cadmium sulfide C-base composte material prepared by inventive method shows the PhotoelectrocatalytiPerformance Performance of excellence as photoelectric, has relatively
High visible light-responded and good light stability.Cadmium sulfide C-base composte material prepared by the inventive method can synthesize in a large number,
Need not expensive device, can be widely used in photocatalysis.
Accompanying drawing explanation
Fig. 1 is the XRD figure of the cadmium sulfide C-base composte material of the present invention;
Fig. 2 is the SEM figure of the cadmium sulfide C-base composte material of the present invention;
Fig. 3 is the TEM figure of the cadmium sulfide C-base composte material of the present invention;
Fig. 4 is the performance characterization that cadmium sulfide C-base composte material of the present invention makees photoelectric;
Fig. 5 is the chemical structural drawing of a, b in background of invention.
Detailed description of the invention
Below in conjunction with the accompanying drawings, the present invention is described in further detail by technical scheme and embodiment.
Embodiment one, according to Fig. 1,2,3,4, a kind of cadmium sulfide C-base composte material is as the preparation of photoelectric
Method, specifically comprises the following steps that
Step one, utilize carrageenan gel principle that the 2g ι that the mass fraction of high-temperature digestion is 2%-carrageenan raw material is instilled
100ml concentration is in the ethanol solution of the hydrochloric acid of 2mol L-1, forms gel, does gel roguing and processes;
Step 2, carrageenan gel after roguing to be immersed 100ml substance withdrawl syndrome be that the ethanol of 1.5mol L-1 cadmium acetate is molten
In liquid, process 3 ~ 5 times;
Step 3, above-mentioned gel ethanol and moisture being walked cleaning 2 ~ 3 times, the gel after processing is put in refrigerator, then
Lyophilization, forms cadmium-carrageenan aeroge;
Step 4, cadmium-carrageenan aeroge through certain carbonization technique calcining, is calcined 1 hour for 700 DEG C in tube furnace, it
After 610 DEG C of de-carbons 1 hour in carbon dioxide again, obtain cadmium sulfide carbon back composite photoelectric catalyst;
Step 5, use electrochemical workstation and xenon lamp systems test the PhotoelectrocatalytiPerformance Performance of above-mentioned cadmium sulfide C-base composte material.
The cadmium sulfide C-base composte material of Fig. 2 SEM figure, hence it is evident that seen from there is good aeroge pattern, substantial amounts of sulfur
Cadmium nano-particle is on aeroge surface.
Use carrageenan, two acetate hydrate cadmium raw materials, successfully prepare the cadmium sulfide carbon back for photoelectrocatalysis multiple
Close catalyst.This catalyst shows excellent photoelectric catalytically active, and (density of photocurrent 100 μ about A, light source is 300W(100W
Cm-2) xenon lamp, electrolyte is metabisulfite solution) and good light stability (4000 seconds density of photocurrent of continuous illumination are hardly
Become).
The technique of traditional fabrication cadmium sulfide, typically using sodium sulfide or hydrogen sulfide as additional sulfur source, in preparation process
Easily produce secondary pollution, furthermore cadmium sulfide is inhaled owing to hole and photoelectronic quick composite table reveal light in photocatalytic process
The low light stability with extreme difference of rate of producing effects, this greatly limits cadmium sulfide application in photocatalysis.Additionally marine biomass
Greatly developing of material, is we provided development opportunity more.Therefore, stable sulfuration is prepared in development simply and easily
The method of cadmium carbon back composite photoelectric catalyst, thus overcome cadmium sulfide preparation and photoelectrocatalysis in defect it is critical that.
In the present invention, carrageenan abundance, resource are extensive, and gained photoelectrocatalysimaterial material shows the performance of excellence, is
The most promising material for photoelectrocatalysis.
Above in conjunction with accompanying drawing, the present invention is exemplarily described, it is clear that the present invention implements not by above-mentioned reality
Execute the restriction of mode.The present invention can be made various on the premise of conceiving without departing from the technology of the present invention by those skilled in the art
Amendment or modification, within these amendments or modification also fall into protection scope of the present invention certainly.
Claims (5)
1. a cadmium sulfide C-base composte material is as the preparation method of photoelectric, it is characterised in that: specifically comprise the following steps that
Step one, utilize the gel principle of carrageenan, the carrageenan raw material of high-temperature digestion is instilled in the ethanol solution of hydrochloric acid, shape
Become gel, do gel roguing and process;
Step 2, after roguing carrageenan gel immerse certain density cadmium acetate ethanol solution in, repeatedly process;
Step 3, above-mentioned gel ethanol and moisture being walked and cleans, the gel after processing is put in refrigerator, then freezing dry
Dry, form cadmium-carrageenan aeroge;
Step 4, cadmium-carrageenan aeroge is calcined through certain carbonization technique in tube furnace, high in carbon dioxide the most again
Temperature de-carbon, obtains cadmium sulfide carbon back composite photoelectric catalyst;
Step 5, use electrochemical workstation and xenon lamp systems test the PhotoelectrocatalytiPerformance Performance of above-mentioned product.
Cadmium sulfide C-base composte material the most according to claim 1 exists as the preparation method of photoelectric, its feature
In: the mass fraction of the carrageenan in described step one is 2 %, and the ethanol solution concentration of hydrochloric acid is 2mol L-1.
Cadmium sulfide C-base composte material the most according to claim 2 exists as the preparation method of photoelectric, its feature
In: the substance withdrawl syndrome of the cadmium acetate in described step 2 is 1.5mol L-1, and number of processes is 3 ~ 5 times.
Cadmium sulfide C-base composte material the most according to claim 3 exists as the preparation method of photoelectric, its feature
In: ethanol and moisture other places in described step 3 are managed 2 ~ 3 times.
Cadmium sulfide C-base composte material the most according to claim 4 exists as the preparation method of photoelectric, its feature
In: the carbonization technique in described step 4 be in nitrogen atmosphere 700 DEG C calcine 1 hour, then in carbon dioxide 610
DEG C de-carbon 1 hour.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610566303.9A CN106268865B (en) | 2016-07-19 | 2016-07-19 | A kind of preparation method of cadmium sulfide C-base composte material as photoelectric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610566303.9A CN106268865B (en) | 2016-07-19 | 2016-07-19 | A kind of preparation method of cadmium sulfide C-base composte material as photoelectric |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106268865A true CN106268865A (en) | 2017-01-04 |
CN106268865B CN106268865B (en) | 2019-11-05 |
Family
ID=57651643
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610566303.9A Active CN106268865B (en) | 2016-07-19 | 2016-07-19 | A kind of preparation method of cadmium sulfide C-base composte material as photoelectric |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106268865B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107188153A (en) * | 2017-06-02 | 2017-09-22 | 青岛大学 | A kind of porous carbon preparation method for material |
CN109999835A (en) * | 2019-03-27 | 2019-07-12 | 武汉理工大学 | A kind of carbonization bacteria cellulose-cadmium sulfide composite photocatalyst material and its preparation method and application |
CN114177922A (en) * | 2021-12-14 | 2022-03-15 | 西南科技大学 | Composite catalyst for removing uranium in nuclear waste liquid and preparation method and application thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103554925A (en) * | 2013-10-09 | 2014-02-05 | 北京理工大学 | Quantum dot doped gel, and preparation and application thereof |
KR20160057703A (en) * | 2014-11-14 | 2016-05-24 | (주)뷰티화장품 | Preparation method of hydrogel mask pack comprising photocatalyst |
-
2016
- 2016-07-19 CN CN201610566303.9A patent/CN106268865B/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103554925A (en) * | 2013-10-09 | 2014-02-05 | 北京理工大学 | Quantum dot doped gel, and preparation and application thereof |
KR20160057703A (en) * | 2014-11-14 | 2016-05-24 | (주)뷰티화장품 | Preparation method of hydrogel mask pack comprising photocatalyst |
Non-Patent Citations (1)
Title |
---|
PERETZ,S.: "Improving the properties of CdS nanoparticles by adding polymers", 《PARTICULATE SCIENCE AND TECHNOLOGY》 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107188153A (en) * | 2017-06-02 | 2017-09-22 | 青岛大学 | A kind of porous carbon preparation method for material |
CN107188153B (en) * | 2017-06-02 | 2019-07-30 | 青岛大学 | A kind of porous carbon preparation method for material |
CN109999835A (en) * | 2019-03-27 | 2019-07-12 | 武汉理工大学 | A kind of carbonization bacteria cellulose-cadmium sulfide composite photocatalyst material and its preparation method and application |
CN109999835B (en) * | 2019-03-27 | 2022-05-10 | 武汉理工大学 | Carbonized bacterial cellulose-cadmium sulfide composite photocatalytic material and preparation method and application thereof |
CN114177922A (en) * | 2021-12-14 | 2022-03-15 | 西南科技大学 | Composite catalyst for removing uranium in nuclear waste liquid and preparation method and application thereof |
CN114177922B (en) * | 2021-12-14 | 2023-09-01 | 西南科技大学 | Composite catalyst for removing uranium in nuclear waste liquid and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
CN106268865B (en) | 2019-11-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110841622B (en) | Controllable In preparation based on MOF template2O3Method for preparing @ ZnO nano heterojunction photocatalytic material | |
CN107837817B (en) | Carbon dot/carbon nitride/titanium dioxide composite material and preparation method and application thereof | |
CN109806888B (en) | 1T-MoS2Modified ZnCoS solid solution hollow dodecahedron nanocomposite and preparation method and application thereof | |
CN106964339B (en) | Carbon-doped ultrathin bismuth tungstate nanosheet photocatalytic material and preparation method thereof | |
CN106268865A (en) | A kind of cadmium sulfide C-base composte material is as the preparation method of photoelectric | |
Dai et al. | ZnIn2S4 modified CaTiO3 nanocubes with enhanced photocatalytic hydrogen performance | |
CN107376957B (en) | Preparation method and application of red phosphorus-coated titanium dioxide nanofiber photocatalytic material | |
CN110252346B (en) | MoS2/SnS2Preparation method and application of/r-GO composite photocatalyst | |
Liu et al. | Tandem cells for unbiased photoelectrochemical water splitting | |
CN111250135B (en) | Graphite-phase carbon nitride nanosheet material and preparation method and application thereof | |
CN107983386B (en) | Ultrathin BiOCl/nitrogen-doped graphene quantum dot composite photocatalyst and preparation method thereof | |
CN106807430A (en) | G C with special clad structure3N4The preparation method of@diatomite composite photocatalytic agent | |
CN114920979B (en) | Modified lignin-based biomass gel and preparation method thereof | |
CN112316969A (en) | N-doped TiO2Hollow microsphere-BiOBr photocatalytic degradation material and preparation method thereof | |
CN113289658A (en) | BN loaded TiO2-SrTiO3Heterojunction photocatalytic degradation material and preparation method thereof | |
CN104638228A (en) | Coaxial carbon-coated bunchy vanadium potassium phosphate nanowire, as well as preparation method and application of nanowire | |
CN111229260B (en) | Cadmium sulfide nanoparticle/molybdenum disulfide nanobelt heterostructure catalyst for hydrogen production by water decomposition under visible light and preparation method thereof | |
CN111266111B (en) | Nickel-doped titanium-oxygen cluster nano catalytic material, preparation method and application | |
CN103272624B (en) | A kind of preparation method of bismuth phosphate photocatalyst | |
CN105233837A (en) | Modified copper bismuthate photocatalyst and preparation method thereof | |
CN114849689B (en) | Heterojunction type composite photocatalytic material and preparation method thereof | |
CN111036255A (en) | Preparation method and application of reed-based SiC/C photocatalytic hydrogen production catalytic material | |
CN105709594A (en) | Method for resourcefully utilizing CO2 in power plant flue gas | |
CN112588304B (en) | Preparation method of bismuth oxybromide efficient photocatalyst with homogenous crystal face junction | |
CN114984937A (en) | Spatially separated double-vacancy titanium dioxide homojunction catalyst and preparation method and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |