CN1644757A - Production of quantum point nanometer titanium dioxide composite membrane - Google Patents
Production of quantum point nanometer titanium dioxide composite membrane Download PDFInfo
- Publication number
- CN1644757A CN1644757A CN 200510018188 CN200510018188A CN1644757A CN 1644757 A CN1644757 A CN 1644757A CN 200510018188 CN200510018188 CN 200510018188 CN 200510018188 A CN200510018188 A CN 200510018188A CN 1644757 A CN1644757 A CN 1644757A
- Authority
- CN
- China
- Prior art keywords
- quantum dot
- titanium dioxide
- composite membrane
- dioxide composite
- nanometer titanium
- 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
Landscapes
- Catalysts (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
This invention was about preparation of quantum dot nanometer Titania complex film. The nanometer Titania film and quantum dot were synthesized first. Then, the quantum dots were modified by the small molecule that can modified to the quantum dot, which with a carboxy group. The quantum dot nanometer titania complex film were synthesized through self packing. Its advantages include good visible light catalysis, good stability, extensive use for sterilization.
Description
Technical field
The present invention relates to a kind of preparation method of quantum point nanometer titanium dioxide composite membrane.
Background technology
At present, the preparation method of quantum point nanometer titanium dioxide composite membrane normally makes nanometer titanium dioxide composite membrane earlier, then nanometer titanium dioxide composite membrane is placed the reaction vessel of preparation quantum dot, in the process of preparation quantum dot, quantum dot is deposited on the nanometer titanium dioxide composite membrane, can not get better controlled owing to be deposited on the particle diameter of the quantum dot on the nanometer titanium dioxide composite membrane, therefore the particle diameter of the quantum dot on the quantum point nanometer titanium dioxide composite membrane is at random, and quantum point nanometer titanium dioxide composite membrane uses under the visible light condition usually, the wavelength of visible light scope is a fixed, so the particle diameter of the quantum dot catalytic capability that can influence quantum point nanometer titanium dioxide composite membrane at random.
Summary of the invention
The present invention is directed to the above-mentioned deficiency of quantum point nanometer titanium dioxide composite membrane, a kind of preparation method of quantum point nanometer titanium dioxide composite membrane is provided, the quantum point nanometer titanium dioxide composite membrane that makes by this method has the excellent visible light catalytic capability, stability is also fine, therefore, can be applied to fields such as sterilization and disinfection widely.
Technical scheme provided by the invention is: a kind of preparation method of quantum point nanometer titanium dioxide composite membrane, and its step is as follows:
(1) method by liquid deposition prepares nano titanium dioxide film;
(2) with the quantum dot of 4nm-8nm, can select for use the core/shell type quantum dot of stable performance to be dissolved in the non-polar solvent, as normal hexane, toluene, chloroform solvent, make the solution that concentration range is a 0.5-2.5mg/ml core/shell type quantum dot;
(3) get the solution that 1ml contains the core/shell type quantum dot,, modify, make the quantum dot surface be with carboxyl as Thiovanic acid, halfcystine, sulfydryl undeeanoic acid with modifying the quantum dot surface and containing the small molecules that carboxyl function is rolled into a ball;
(4) quantum dot after will modifying is dissolved in and makes the quantum dot solution that concentration range is 0.1-1mg/ml in the suitable quantity of water, the nano titanium dioxide film that will make immerses in the solution of this quantum dot then, placed 6-24 hour down at 1-30 ℃, taking-up dries up with big water gaging flushing, promptly obtains quantum point nanometer titanium dioxide composite membrane.
The present invention adopts the stepwise synthesis method of self-assembly then, elder generation is synthesis of nano titanium dioxide film and core/shell type quantum dot respectively, choosing required particle diameter quantum dot then modifies with small molecules, method by self-assembly makes quantum point nanometer titanium dioxide composite membrane at last, the quantum point nanometer titanium dioxide composite membrane of this method preparation is concentrated because of quantum point grain diameter, so have the excellent visible light catalytic capability, make for self-assembly because of it again, stability is also fine, and this preparation method is workable, and is simple.
Embodiment
The present invention adopts the stepwise synthesis method of self-assembly then, and its specific embodiment is as follows:
(1) method by liquid deposition prepares nano titanium dioxide film;
(2) be that the core/shell type quantum dot of 4nm-8nm is dissolved in the normal hexane with the particle diameter that makes, making concentration is the hexane solution of the core/shell type quantum dot of 1mg/ml, the CdSe/ZnS core/shell type quantum dot that the core/shell type quantum dot can adopt the preparation method of ZL02139152.1 patent disclosure to make;
(3) get the above-mentioned hexane solution that contains the core/shell type quantum dot of 1ml, quantum dot is modified by ordinary method with the small molecules that can modify quantum dot surface and contain carboxyl function group, concrete operations are for adding 1ml methyl alcohol eccentric cleaning and be dispersed in 0.5mlN in solution earlier, in the dinethylformamide, on shaking table, vibrated 30 minutes after adding the 0.5ml Thiovanic acid again, make carboxyl in the quantum dot finishing, add the centrifugation of 1ml tetrahydrofuran (THF) then and go out carboxylated quantum dot;
(4) carboxylated quantum dot is dissolved in the 1ml water, then the nano titanium dioxide film that makes is immersed in this solution, placed 12 hours down at 4 ℃, taking-up dries up with big water gaging flushing, promptly obtains quantum point nanometer titanium dioxide composite membrane.
Adopt aforesaid method of the present invention also can to self-assemble on the nanometer titanium dioxide composite membrane by the quantum dot that other is carboxylated.
Claims (4)
1. the preparation method of a quantum point nanometer titanium dioxide composite membrane is characterized in that adopting following step:
(1) method by liquid deposition prepares nano titanium dioxide film;
(2) quantum dot with 4nm-8nm is dissolved in the non-polar solvent, makes the solution that concentration range is the 0.5-2.5mg/m1 quantum dot;
(3) get the solution that contains quantum dot in right amount, use the small molecules that to modify the quantum dot surface and contain carboxyl function group to modify, make the quantum dot surface be with carboxyl by ordinary method;
(4) quantum dot after will modifying is dissolved in and makes the quantum dot solution of concentration range at 0.1-1mg/ml in the suitable quantity of water, the nano titanium dioxide film that will make immerses in the solution of this quantum dot then, placed 6-24 hour down at 1-30 ℃, taking-up dries up with big water gaging flushing, promptly obtains quantum point nanometer titanium dioxide composite membrane.
2. the preparation method of quantum point nanometer titanium dioxide composite membrane according to claim 1, it is characterized in that: quantum dot can be selected the core/shell type quantum dot for use.
3. the preparation method of quantum point nanometer titanium dioxide composite membrane according to claim 1 and 2, it is characterized in that: non-polar solvent is normal hexane, toluene, chloroform.
4. the preparation method of quantum point nanometer titanium dioxide composite membrane according to claim 1 and 2, it is characterized in that: small molecules is Thiovanic acid, halfcystine, sulfydryl undeeanoic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100181883A CN1332065C (en) | 2005-01-24 | 2005-01-24 | Production of quantum point nanometer titanium dioxide composite membrane |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100181883A CN1332065C (en) | 2005-01-24 | 2005-01-24 | Production of quantum point nanometer titanium dioxide composite membrane |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1644757A true CN1644757A (en) | 2005-07-27 |
CN1332065C CN1332065C (en) | 2007-08-15 |
Family
ID=34875682
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2005100181883A Expired - Fee Related CN1332065C (en) | 2005-01-24 | 2005-01-24 | Production of quantum point nanometer titanium dioxide composite membrane |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1332065C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103464014A (en) * | 2013-09-25 | 2013-12-25 | 天津工业大学 | Method for inhibiting bacteria on surface of hollow fiber membrane |
CN105388660A (en) * | 2015-12-17 | 2016-03-09 | 深圳市华星光电技术有限公司 | Preparation method of COA type array substrate |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09102596A (en) * | 1995-10-04 | 1997-04-15 | Fujitsu Ltd | Manufacture of quantum dot and quantum dot apparatus |
CN1054166C (en) * | 1997-11-14 | 2000-07-05 | 中国科学院固体物理研究所 | Preparing method for inlaid dimension controllable nanometre grade silver particle on barium titanate film |
CN1193117C (en) * | 2001-05-17 | 2005-03-16 | 上海大学 | Process for preparing optically catalytic TiO2 film |
-
2005
- 2005-01-24 CN CNB2005100181883A patent/CN1332065C/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103464014A (en) * | 2013-09-25 | 2013-12-25 | 天津工业大学 | Method for inhibiting bacteria on surface of hollow fiber membrane |
CN105388660A (en) * | 2015-12-17 | 2016-03-09 | 深圳市华星光电技术有限公司 | Preparation method of COA type array substrate |
CN105388660B (en) * | 2015-12-17 | 2018-05-01 | 深圳市华星光电技术有限公司 | The preparation method of COA type array base paltes |
Also Published As
Publication number | Publication date |
---|---|
CN1332065C (en) | 2007-08-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Caminade et al. | Dendrimers and nanotubes: a fruitful association | |
WO2002072930A1 (en) | Metallic nanowire and process for producing the same | |
Azzouz et al. | Potential applications of deep eutectic solvents in nanotechnology: Part II | |
Adimule et al. | Recent advances in the one-pot synthesis of coumarin derivatives from different starting materials using nanoparticles: a review | |
Son et al. | Interference of solvatochromic twist in amyloid nanostructure for light-driven biocatalysis | |
Xiong et al. | Synthesis and characterization of renewable woody nanoparticles fluorescently labeled by pyrene | |
CN1644757A (en) | Production of quantum point nanometer titanium dioxide composite membrane | |
CN110368826A (en) | A kind of preparation method of the pickering emulsion of magnetic field and redox double-response | |
CN111378147A (en) | Novel chiral MOF material and preparation method and application thereof | |
FR2729586A1 (en) | PROCESS FOR THE SYNTHESIS OF ALDEHYDES AND THEIR DERIVATIVES AND CATALYST FOR SELECTIVE REDUCTION OF CARBOXYLIC DERIVATIVES TO ALDEHYDES | |
Yamauchi et al. | Fabrication of a Pt film with a well-defined hierarchical pore system via “solvent-evaporation-mediated direct physical casting” | |
Ma et al. | Enzyme immobilization on a novel NH2-MOF-5@ PEI composite support for efficient kinetic resolution of MOPE enantiomers | |
Li et al. | Recent advances of chiral metal-organic framework in analytic chemistry | |
JP2007320902A (en) | Chlorophyll nanoparticle and method for producing the same | |
CN108358299A (en) | A kind for the treatment of process of ozone catalytic degradation of dye waste water | |
CN110327973A (en) | A kind of crosslinking norbornene copolymer/carbon black three-dimensional network supported copper nanocatalyst and the preparation method and application thereof | |
CN1986043A (en) | Preparing process of liquid chromatography stuffing | |
CN114891517A (en) | Rosin-based CO 2 /N 2 Responsive microemulsion and preparation method and application thereof | |
Gálvez-Martínez et al. | Catalytic evaluation of citrate-stabilized palladium nanoparticles in the Sonogashira reaction for the synthesis of 1, 4-Bis [(trimethylsilyl) ethynyl] benzene | |
Zhou et al. | Multifunctional CuS-based micro-flower loaded with carbon dots/laccase for effectively detection and removal of catechol | |
FR3063994A1 (en) | PROCESS FOR SYNTHESIS OF MULTIPLE SEEDING OF ZEOLITAN CRYSTALS WITH CONTROLLED GRANULOMETRY | |
Shi et al. | C 60 based nanoparticles: self-assembly of a novel fullerene derivative | |
JP5354591B2 (en) | AMIDE COMPOUND HAVING PHOTOISOMERIZATION GROUP, ORGANIC NANOTUBE COMPRISING SELF-ASSEMBLING THE COMPOUND, AND METHOD FOR PRODUCING THE SAME | |
EP3380586B1 (en) | Method for synthesizing hydrocarbons from a syngas in the presence of a cobalt catalyst trapped in a mesoporous oxide matrix and obtained from at least one colloidal precursor | |
CN112920426B (en) | Rosin-based calcium salt supermolecule hydrogel, preparation method and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070815 Termination date: 20130124 |
|
CF01 | Termination of patent right due to non-payment of annual fee |