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Transition metal in-situ doped TiO2 catalyst as well as preparation method and application thereof

A transition metal, in-situ doping technology, applied in catalyst activation/preparation, metal/metal oxide/metal hydroxide catalyst, physical/chemical process catalyst, etc., can solve the limitation of catalytic performance modulation and application range, The overall performance of the catalyst is greatly affected, and the distribution of metal atoms is not uniform, so that the experimental conditions are easy to control, the production cost is low, and the structure is stable.

Active Publication Date: 2021-07-30
TIANJIN POLYTECHNIC UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Currently, many experimental protocols have been proposed to prepare metal-doped M-TiO 2 However, the existing methods have the following disadvantages to varying degrees: (1) the experimental scheme involves dangerous strong acids (such as concentrated sulfuric acid, concentrated nitric acid, hydrofluoric acid, etc.) or expensive reagents
(2) The drastic preparation method (such as plasma bombardment, laser method, etc.) is used, which is not suitable for large-scale production, and the distribution of metal atoms doped is not uniform. For M-TiO 2 The overall performance of the catalyst is greatly affected
(3) Many prepared M-TiO 2 The key parameters such as the type, doping amount, and existing form of metal elements in the catalyst have little room for regulation, which greatly limits the modulation and application range of its catalytic performance.

Method used

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  • Transition metal in-situ doped TiO2 catalyst as well as preparation method and application thereof
  • Transition metal in-situ doped TiO2 catalyst as well as preparation method and application thereof
  • Transition metal in-situ doped TiO2 catalyst as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Weigh 0.1g of H 2 Ti 3 o 7 The raw material is added to 40 mL of an aqueous solution of cuprous chloride with a concentration of 0.1 mol / L under the assistance of ultrasound, and the ultrasound is continued for 5-10 minutes to obtain a uniformly dispersed suspension. The suspension was continuously stirred by magnetic force for 24 h at room temperature, and the H 2 Ti 3 o 7 H in + Ions and Cu in solution + The ion exchange reaches equilibrium, and the complete Cu exchange is obtained by filtration. x h 2- x Ti 3 o 7 The samples (x is the atomic ratio, 0x h 2-x Ti 3 o 7 The sample was calcined in a tube furnace, fed with air, and then the temperature was raised from room temperature to 700 °C at a rate of 5 °C / min, and kept at this temperature for 2 h, and then naturally cooled to room temperature, and the brown Cu atomic atoms were collected. Site-doped Cu-TiO 2 Catalyst, the XRD collection of patterns of gained material such as figure 1 As shown, it can...

Embodiment 2

[0032] Weigh 0.1g of H 2 Ti 3 o 7 The raw material is added to 50 mL of an aqueous solution of zinc acetate with a concentration of 0.1 mol / L under the assistance of ultrasound, and the ultrasound is continued for 5-10 minutes to obtain a uniformly dispersed suspension. The suspension was continuously stirred by magnetic force for 24 h at room temperature, and the H 2 Ti 3 o7 H in + Ions and Zn in solution 2+ The ion exchange reaches equilibrium, and the Zn that is completely exchanged is filtered x h 2- x Ti 3 o 7 The samples (x is the atomic ratio, 0x h 2-x Ti 3 o 7 The sample was calcined in a tube furnace, fed with air, and then the temperature was raised from room temperature to 800 °C at a rate of 10 °C / min, and kept at this temperature for 2 hours, then naturally cooled to room temperature, and gray-black Zn atoms were collected. In-situ doped Zn-TiO 2 catalyst.

Embodiment 3

[0034] Weigh 0.5g of H 2 Ti 3 o 7 The raw material is added to 100 mL of silver nitrate aqueous solution with a concentration of 0.05 mol / L under the assistance of ultrasound, and the ultrasound is continued for 5-10 minutes to obtain a uniformly dispersed suspension. The suspension was continuously stirred by magnetic force for 22 h at room temperature, and the H 2 Ti 3 o 7 H in + Ions and Ag in solution + The ion exchange reaches equilibrium, and the complete Ag exchange is obtained by filtration. x h 2- x Ti 3 o 7 The samples (x is the atomic ratio, 0x h 2-x Ti 3 o 7 The sample was calcined in a tube furnace, fed with air, and then the temperature was raised from room temperature to 750 °C at a rate of 5 °C / min, and kept at this temperature for 2 hours, and then naturally cooled to room temperature, and gray-blue Ag was collected. Atomically doped Ag-TiO 2 catalyst.

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Abstract

The invention relates to a transition metal in-situ doped TiO2 catalyst as well as a preparation method and application thereof. H2Ti3O7 is used as a raw material, ion exchange is carried out in a transition metal cation aqueous solution to obtain an MxH2-xTi3O7 precursor, H2-xTi3O7 is converted into a TiO2 matrix through high-temperature calcination, exchanged Mn < + > is doped into a TiO2 crystal lattice in situ in a transition metal monatomic or polyatomic form, and the transition metal atom in-situ doped M-TiO2 material on an atomic level is prepared. The preparation method is simple in process route, simple and convenient to operate, high in dispersion degree of doped ions, good in uniformity, simple in required equipment and easy to amplify production, and the prepared transition metal in-situ doped M-TiO2 catalyst material shows better application prospects in the fields of water treatment, catalytic oxidation, energy storage, sensing and the like.

Description

technical field [0001] The invention belongs to the technical field of catalyst preparation, in particular to a transition metal in-situ doped TiO 2 Catalyst, preparation method and application. Background technique [0002] TiO 2 The material is a common industrial raw material, not only low in price, non-toxic and pollution-free, high temperature resistance, acid and alkali resistance, stable chemical properties, and strong interaction with metals, it is an ideal catalyst carrier material. [0003] In addition, TiO 2 The material was also found to have good photoelectrochemical properties and can be used as a photocatalyst to exhibit good catalytic activity in multiple chemical reactions. But pure TiO 2 There are still two major shortcomings in photocatalysts, so that they have not been really applied in industrial photocatalytic production: (1) TiO 2 The intrinsic bandgap of is too large (3.2eV), so that it can only be excited by ultraviolet light and cannot respond ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/72B01J21/06B01J23/06B01J23/50B01J23/745B01J23/75B01J23/10B01J23/755B01J23/44B01J23/52B01J23/34B01J23/42B01J23/46B01J23/08B01J23/18B01J37/30B01J37/08C02F1/30C07D295/24C02F101/30C02F101/34C02F101/38
CPCB01J23/72B01J21/063B01J23/06B01J23/50B01J23/745B01J23/75B01J23/10B01J23/755B01J23/44B01J23/52B01J23/34B01J23/42B01J23/462B01J23/08B01J23/18B01J37/30B01J37/082C02F1/30C07D295/24C02F2101/30C02F2101/34C02F2101/38C02F2305/10B01J35/394B01J35/39Y02P20/52
Inventor 张鹏杨晓燕李静茹王佳任尹良科
Owner TIANJIN POLYTECHNIC UNIV
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