Preparation method of graphite-phase carbon nitride with large specific surface area

A technology of graphite phase carbon nitride and large specific surface area, which is applied in the fields of chemical instruments and methods, inorganic chemistry, hydrogen production, etc. It can solve the problems that the template agent does not conform to green chemistry, is volatile and corrosive, and improves the specific surface area. , to avoid structural defects and environmental pollution, fast transfer speed, and improve performance

Inactive Publication Date: 2019-12-13
LIAONING UNIVERSITY OF PETROLEUM AND CHEMICAL TECHNOLOGY
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But the technology requires HF, NH 4 HF 2 Etching with other template agents, the process is complex and volatile and corrosive HF, NH 4 HF 2 Templating agents also do not meet the requirements of green chemistry
The soft stencil agent mainly synthesizes the ordered mesoporous graphite phase carbon nitride by the self-assembly method of the surfactant, which emphasizes the chemical matching between the organic phase and the inorganic phase, and the specific surface area of ​​the prepared porous graphite phase carbon nitride is 84m 2 / g, although this method is simple to operate, but due to g-C 3 N 4 The CN structure will extend at high temperature, g-C 3 N 4 The condensation temperature of the soft template is obviously higher than the decomposition temperature of the soft template, and the premature removal of the soft template will cause the pores to close, and the improvement of the specific surface area is limited.
However, like using concentrated sulfuric acid or concentrated hydrochloric acid for precursor pretreatment, although a porous graphite phase carbon nitride with a large specific surface area is obtained, the use of concentrated acid will still cause certain safety hazards.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of graphite-phase carbon nitride with large specific surface area
  • Preparation method of graphite-phase carbon nitride with large specific surface area
  • Preparation method of graphite-phase carbon nitride with large specific surface area

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0028] The preparation method of graphite phase carbon nitride with large specific surface area is implemented as follows:

[0029] (1) Take a certain amount of nitrogen-containing precursor into a three-necked flask;

[0030] (2) Put the three-necked flask containing the nitrogen-containing precursor into the oil bath, and heat and stir for 0.5-2h under the heating condition of 135~180℃;

[0031] (3) After the heating and stirring are completed, take the three-necked flask out of the oil bath, wait for the molten urea to cool and crystallize at room temperature, grind the obtained solid crystals into powder, and then roast it in an air atmosphere;

[0032] The specific steps are as follows: in the muffle furnace, the temperature is raised to 200°C at a temperature rise rate of 5-20°C / min and kept for 0.5-2h. After keeping it for a certain period of time, the temperature is increased to 400-650°C at a heating rate of 5-20°C / min, and it is calcined for 1 to 4 hours.

[0033] In the abov...

Embodiment 1

[0044] (1) Put the three-necked flask containing 25g of urea into the oil bath, the temperature of the oil bath is 135 o C, heating and stirring for 2h. The molten urea is cooled and crystallized at room temperature.

[0045] (2) Grind the obtained solid crystals into powder, put them in a crucible and cover them, and put the covered crucible into the muffle furnace. o C / min heating rate, first heating up to 200 o Keep C for 1h, then heat up to 400 o C, roasting for 4h. It is naturally cooled to room temperature, and the solid product is ground to obtain graphite phase carbon nitride with a large specific surface area.

Embodiment 2

[0047] (1) Put the three-necked flask with 25g of urea into the oil bath, the temperature of the oil bath is 140 o C, heating and stirring for 1.5h. The molten urea is cooled and crystallized at room temperature.

[0048] (2) Grind the obtained solid crystal into powder, put it in a crucible, cover it, put the covered crucible into the muffle furnace, and reduce it to 10 o C / min heating rate, first heating up to 200 o Keep C for 1h, then heat up to 450 o C, roasting for 3h. It is naturally cooled to room temperature, and the solid product is ground to obtain graphite phase carbon nitride with a large specific surface area.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
specific surface areaaaaaaaaaaa
pore sizeaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to view more

Abstract

The invention belongs to the field of visible light catalytic materials, and particularly relates to a method for preparing a large-specific-surface-area graphite-phase carbon nitride material by utilizing a low-melting-point precursor and carrying out low-temperature heat treatment on the precursor in a roasting process. The preparation method comprises the following steps: (1) putting a nitrogen-containing precursor into a three-necked flask, putting the three-necked flask filled with the nitrogen-containing precursor into an oil bath pot after the temperature of the oil bath pot reaches themelting point of the nitrogen-containing precursor, and heating and stirring to enable the nitrogen-containing precursor to be in a molten state; (2) heating to keep a molten state, taking out the three-neck flask, and cooling and crystallizing the nitrogen-containing precursor at the molten state at room temperature; and (3) grinding the crystallized nitrogen-containing precursor into powder, putting the powder into a crucible, putting the crucible into a muffle furnace, carrying out programmed heating, and roasting in an air atmosphere to obtain a target product. The method has the advantages of simple process, environmental protection, low cost, high purity of the target product, and high catalytic performance.

Description

Technical field [0001] The invention belongs to the field of visible light catalytic materials, and specifically relates to a method for preparing a graphite phase carbon nitride material with a large specific surface area by using a precursor with a low melting point and low-temperature heat treatment of the precursor during a roasting process. Background technique [0002] At present, human society is facing the two thorny problems of environmental pollution and energy crisis. A lot of research has been devoted to the development of green and efficient semiconductor photocatalysts, which are used to photocatalyze the decomposition of water to produce hydrogen and degrade pollutants in water and gas to solve Environmental energy issues. Among them, the core of visible light catalysis technology is to explore and develop a green-friendly, cheap and easy-to-obtain visible light catalyst with high efficiency and excellent performance. [0003] In recent years, graphite phase carbon ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): B01J27/24C01B3/04C02F1/30C02F1/72C02F101/38
CPCB01J27/24B01J35/004B01J35/1014B01J35/1019B01J35/1061B01J35/1066C02F1/30C02F1/725C01B3/042C01B2203/0277C01B2203/1041C02F2101/38Y02E60/36
Inventor 张健刘帅李旭贺王彦娟王海彦胡绍争封瑞江白金其他发明人请求不公开姓名
Owner LIAONING UNIVERSITY OF PETROLEUM AND CHEMICAL TECHNOLOGY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products