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Graphite phase carbon nitride quantum dot and preparation method thereof

A graphitic carbon nitride, quantum dot technology, applied in chemical instruments and methods, nitrogen and non-metallic compounds, nanotechnology for materials and surface science, etc. Large-scale production, uneven quantum size, etc., to achieve the effects of high yield, short production cycle, and simple preparation method

Active Publication Date: 2016-08-24
SHANDONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

But the synthesized quantum size is not uniform
Chun-yang Zhang research group 5 The performance of graphitic carbon nitride quantum dots synthesized by high pressure method is better, but this method is not suitable for large-scale mass production
[0006] In summary, there are various deficiencies in the methods for preparing graphite-phase carbon nitride quantum dots in the above two types: either the preparation process is complicated, the production cycle is long, the yield is low, and it is not suitable for large-scale production; or it is used in raw materials and preparation processes. Materials that are harmful to the environment and health; or the size of the prepared quantum dots is not good, and the performance is not good, which is not conducive to practical use

Method used

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  • Graphite phase carbon nitride quantum dot and preparation method thereof
  • Graphite phase carbon nitride quantum dot and preparation method thereof
  • Graphite phase carbon nitride quantum dot and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] ①Dissolve urea and sodium chloride in 100mL of deionized water at a molar ratio of 40:1, stir well and mix evenly to make a colorless and transparent solution with a urea concentration of 6mol / L;

[0033] ②Place the prepared colorless transparent solution in a liquid nitrogen environment for 10 minutes, so that the solution is rapidly frozen into a whole, and a uniform white block solid is obtained;

[0034]③Quickly transfer the obtained massive solid to a vacuum freeze dryer at -80°C, set the vacuum degree to 8Pa, and freeze-dry for 48 hours to dry the solid to constant weight;

[0035] ④ Place the obtained solid in a crucible with a cover, and put it in an atmosphere furnace with a nitrogen flow rate of 7mL / min, raise the temperature to 500°C at 5°C / min, and keep it for 4h, then cool down with the furnace to obtain a light yellow color sample;

[0036] ⑤ The prepared light yellow sample is uniformly dispersed in deionized water, centrifuged at a speed of 800rpm for 3...

Embodiment 2

[0039] ① Dissolve urea and sodium chloride in 50 mL of deionized water at a molar ratio of 5:1, stir well and mix evenly to make a colorless and transparent solution with a urea concentration of 3 mol / L;

[0040] ②Place the prepared colorless transparent solution in a liquid nitrogen environment for 5 minutes, so that the solution is rapidly frozen into a whole, and a uniform white block solid is obtained;

[0041] ③Quickly transfer the obtained massive solid to a vacuum freeze dryer at -70°C, set the vacuum degree to 10Pa, and freeze-dry for 36 hours to dry the solid to constant weight;

[0042] ④Put the obtained solid in a crucible with a cover, and put it in an atmosphere furnace with a nitrogen flow rate of 3mL / min, raise the temperature to 600°C at 15°C / min, and keep it for 2h, then cool down with the furnace to get a light yellow color sample;

[0043] ⑤ The prepared light yellow sample is evenly dispersed in deionized water, centrifuged at a speed of 1500rpm for 10nm, ...

Embodiment 3

[0045] ①Dissolve urea and sodium chloride in 100mL deionized water at a molar ratio of 10:1, stir well and mix well to make a colorless and transparent solution with a urea concentration of 4mol / L;

[0046] ②Place the prepared colorless transparent solution in a liquid nitrogen environment for 10 minutes, so that the solution is rapidly frozen into a whole, and a uniform white block solid is obtained;

[0047] ③Quickly transfer the obtained massive solid to a vacuum freeze dryer at -80°C, set the vacuum degree to 8Pa, and freeze-dry for 48 hours to dry the solid to constant weight;

[0048] ④ Place the obtained solid in a crucible with a cover, and place it in an atmosphere furnace with a nitrogen flow rate of 5mL / min, raise the temperature to 550°C at 10°C / min, and keep it warm for 3h, then cool down with the furnace to obtain a light yellow color sample;

[0049] ⑤ The prepared light yellow sample is evenly dispersed in deionized water, centrifuged at a speed of 1000rpm for...

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Abstract

The invention discloses a graphite phase carbon nitride quantum dot and a preparation method thereof. The preparation method comprises the steps that urea and sodium chloride are prepared into a urea solution according to the molar ratio, and quick freezing is carried out to obtain even white blocky solid; then, the white blocky solid is transferred to a vacuum freeze dryer to be frozen and dried to constant weight, calcination is carried out in a nitrogen atmosphere furnace to obtain a solid, a faint yellow powder sample is obtained, and the sample is centrifuged, dialyzed and purified to obtain the faint yellow graphite phase carbon nitride quantum dot. The method is simple, practical, suitable for laboratory preparation and industrial production, wide in development space and huge in application prospect.

Description

technical field [0001] The invention relates to a carbon nitride quantum dot and a preparation method thereof, in particular to a graphite phase carbon nitride quantum dot and an environmentally friendly, low-cost, high-yield, high-performance preparation method of a graphite phase carbon nitride quantum dot, which belongs to the material Preparation technology field. Background technique [0002] Carbon Nitride (C 3 N 4 ) is composed of two elements carbon and nitrogen widely found in nature. At the same time, carbon nitride has many attractive properties, such as heat resistance, chemical corrosion resistance, wear resistance, superhardness, waterproof, low density, non-toxicity, and good biocompatibility, which makes carbon nitride a A very important functional material without metal elements. Among them, graphitic carbon nitride (g-C 3 N 4 ) has a graphite-like layered structure and contains very stable triazine (Triazine) and three-s-triazine (Tri-s-triazine) unit...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B21/082B82Y30/00C09K11/65
CPCB82Y30/00C01B21/082C01P2004/04C01P2004/64C09K11/65
Inventor 桑元华郭岱东赵莉莉蔡宁宁李海东马保金刘伟刘宏
Owner SHANDONG UNIV