NiTi nanoflower hydrotalcite photocatalyst as well as preparation method and application thereof

A nanoflower and catalyst technology, applied in the field of NiTi hydrotalcite photocatalyst and its preparation, can solve the problems of unfavorable application, limited reaction conditions, etc., and achieve the advantages of simple preparation method, low requirements on reaction conditions, and improved apparent quantum efficiency. Effect

Active Publication Date: 2020-07-14
SOUTH CHINA UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The existing synthesis methods include low-saturation co-precipitation method, hydrothermal synthesis method, ion exchange method, microwave crystallization method, etc. (Journal of the

Method used

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  • NiTi nanoflower hydrotalcite photocatalyst as well as preparation method and application thereof
  • NiTi nanoflower hydrotalcite photocatalyst as well as preparation method and application thereof
  • NiTi nanoflower hydrotalcite photocatalyst as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] A preparation method of nickel-titanium nano flower hydrotalcite photocatalyst, comprising the steps of:

[0038] (1) Dissolve 0.29g of nickel nitrate hexahydrate, 0.237g of titanium sulfate and 2.8g of urotropine into 50 mL of deionized water, stir well to obtain a transparent solution;

[0039] (2) Transfer the transparent solution described in step (1) to a polytetrafluoroethylene lining and heat up in a muffle furnace for a heating reaction. The temperature of the heating reaction is 140°C, and the heating reaction time is 9 hours. Cool to room temperature. The heated product was obtained, and the precipitate was collected by suction filtration;

[0040] (3) drying the precipitate in step (2) at 30° C. to obtain the nickel-titanium nanoflower hydrotalcite photocatalyst.

Embodiment 2

[0042] A preparation method of nickel-titanium nano flower hydrotalcite photocatalyst, comprising the steps of:

[0043] (1) Dissolve 0.8721g of nickel nitrate hexahydrate, 0.237g of titanium sulfate and 2.8g of urotropine into 50 mL of deionized water, stir well to obtain a transparent solution;

[0044] (2) Transfer the transparent solution described in step (1) to a polytetrafluoroethylene lining and heat up in a muffle furnace for a heating reaction. The temperature of the heating reaction is 140°C, and the heating reaction time is 9 hours. Cool to room temperature. The heated product was obtained, and the precipitate was collected by suction filtration;

[0045] (3) drying the precipitate in step (2) at 60° C. to obtain the nickel-titanium nanoflower hydrotalcite photocatalyst.

[0046] The effect that the nickel-titanium nano flower hydrotalcite photocatalyst that embodiment 2 makes is observed under the scanning electron microscope is as follows: figure 1 shown, from ...

Embodiment 3

[0048] A preparation method of nickel-titanium nano flower hydrotalcite photocatalyst, comprising the steps of:

[0049] (1) Dissolve 1.45g of nickel nitrate hexahydrate, 0.237g of titanium sulfate and 2.8g of urotropine into 50 mL of deionized water, stir well to obtain a transparent solution;

[0050] (2) Transfer the transparent solution described in step (1) to a polytetrafluoroethylene lining and heat up in a muffle furnace for a heating reaction. The temperature of the heating reaction is 140°C, and the heating reaction time is 9 hours. Cool to room temperature. The heated product was obtained, and the precipitate was collected by suction filtration;

[0051] (3) drying the precipitate in step (2) at 100° C. to obtain the nickel-titanium nanoflower hydrotalcite photocatalyst.

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Abstract

The invention discloses a NiTi hydrotalcite photocatalyst as well as a preparation method and an application thereof. The catalyst is three-dimensional NiTi nanometer, and the diameter of the nanoflower is 6-7 [mu] m. The preparation method comprises the following steps: dissolving titanium salt, nickel salt and urotropine in water, and stirring the solution until the solution is transparent; heating the reaction system for a reaction; and cooling and drying after heating to obtain the nickel-titanium nano-flower hydrotalcite photocatalyst, wherein the nickel-titanium nano-flower hydrotalcitephotocatalyst can be used for catalyzing xylose to be converted into xylonic acid. The catalyst is very simple and convenient to synthesize in the aspect of catalyst preparation, high-temperature heating is not needed, and the synthesized catalyst can be directly used for catalytic reaction without subsequent treatment. The catalyst provided by the invention has industrial potential, is low in catalytic process cost, is different from traditional thermal catalysis, is green and environment-friendly in process, and does not generate harmful byproducts.

Description

technical field [0001] The invention belongs to the interdisciplinary technical fields of catalytic materials, photocatalysis, and biomass conversion into chemicals, and in particular relates to a NiTi hydrotalcite photocatalyst, a preparation method and application thereof. Background technique [0002] The sugars available in plant cellulose resources are mainly cellulose and hemicellulose, and the glucose fermentation industry using cellulose as raw material is relatively mature. However, xylose-based hemicellulose in plant fibers accounts for about 20% to 35%, and its efficient conversion and utilization has become one of the key technical bottlenecks of the entire biorefinery system. In recent years, xylonic acid, as an emerging product of high-efficiency biotransformation and utilization of plant fiber resource xylose, has broad industrial application potential, and has been identified by the U.S. Department of Energy as the most promising 30 target products or chemica...

Claims

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Application Information

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IPC IPC(8): B01J23/755B01J37/10C07C51/295C07C59/105
CPCB01J23/755B01J35/004B01J37/10C07C51/295C07C59/105
Inventor 彭新文李铭赛钟林新刘泽昊陈亮
Owner SOUTH CHINA UNIV OF TECH
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