Unlock instant, AI-driven research and patent intelligence for your innovation.

Synthesis method of super-macroporous aluminum phosphate and heteroatom aluminum phosphate molecular sieve with-CLO structure

A technology of aluminum phosphate molecular sieve and heteroatom, which is applied in the field of synthesis of aluminum phosphate and heteroatom aluminum phosphate ultra-large-pore molecular sieve, can solve the problems of high synthesis cost and environmental pollution, and achieve low synthesis cost, environmental friendliness and high yield of molecular sieve Effect

Inactive Publication Date: 2021-06-11
BEIJING UNIV OF CHEM TECH
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, at present, the synthesis of -CLO structure aluminum phosphate and heteroatom aluminum phosphate ultra-large pore molecular sieves adopts ion thermal or solvothermal method, using a large number of ionic liquids, eutectic mixtures, organic amines, surfactants, etc. as solvents and templates. , which inevitably brings problems of environmental pollution and expensive synthesis

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
  • Synthesis method of super-macroporous aluminum phosphate and heteroatom aluminum phosphate molecular sieve with-CLO structure
  • Synthesis method of super-macroporous aluminum phosphate and heteroatom aluminum phosphate molecular sieve with-CLO structure
  • Synthesis method of super-macroporous aluminum phosphate and heteroatom aluminum phosphate molecular sieve with-CLO structure

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Add 374 μl phosphoric acid (concentration is 85wt%) in the 50ml glass beaker, under the condition of keeping 110 ℃ and stirring, add 968 μl tetraethylammonium hydroxide (concentration is 25wt%), 242 μl hydrofluoric acid (concentration is 40wt%) ), 1.12 g of aluminum isopropoxide, and the initial reaction mixture was kept at 110° C. for 30 min, and the initial reaction mixture was a pure white solid. The pure white solid was then placed in a stainless steel reaction kettle lined with polytetrafluoroethylene, sealed and placed in an oven at 180°C for crystallization for 4 hours.

[0031] After the crystallization was completed, the reactor was taken out, cooled to room temperature, the product was washed with deionized water, filtered, and the separated product was dried in an oven at 90°C for 3 hours to obtain a white powder product. The product was analyzed by XRD, and the results showed that the obtained product had an aluminum phosphate-based ultra-large pore molecula...

Embodiment 2

[0033] Add 374 μl phosphoric acid (concentration is 85wt%) in the 50ml glass beaker, under the condition of keeping 110 ℃ and stirring, add 645 μl tetraethylammonium hydroxide (concentration is 25wt%), 242 μl hydrofluoric acid (concentration is 40wt%) ), 1.12 g of aluminum isopropoxide, and the initial reaction mixture was kept at 110° C. for 30 min, and the initial reaction mixture was a pure white solid. The pure white solid was then placed in a stainless steel reaction kettle lined with polytetrafluoroethylene, sealed and placed in an oven at 180°C for crystallization for 4 hours.

[0034] After the crystallization was completed, the reactor was taken out, cooled to room temperature, the product was washed with deionized water, filtered, and the separated product was dried in an oven at 90°C for 3 hours to obtain a white powder product. The product was analyzed by XRD, and the results showed that the obtained product had an aluminum phosphate-based ultra-large pore molecular ...

Embodiment 3

[0036] Add 374 μl phosphoric acid (concentration is 85wt%) in the 50ml glass beaker, under the condition of keeping 110 ℃ and stirring, add 968 μl tetraethylammonium hydroxide (concentration is 25wt%), 242 μl hydrofluoric acid (concentration is 40wt%) ), 1.12g of aluminum isopropoxide, and 0.49g of titanium nitrate. The initial reaction mixture was kept at 110° C. and continued to stir for 30 min, so that the initial reaction mixture was a pure white solid. The pure white solid was then placed in a stainless steel reaction kettle lined with polytetrafluoroethylene, sealed and placed in an oven at 180°C for crystallization for 4 hours.

[0037] After the crystallization was completed, the reactor was taken out, cooled to room temperature, the product was washed with deionized water, filtered, and the separated product was dried in an oven at 90°C for 3 hours to obtain a white powder product. The product was analyzed by XRD, and the results showed that the obtained product had a...

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

No PUM Login to View More

Abstract

The invention discloses a synthetic method of a super-macroporous aluminum phosphate molecular sieve with a-CLO structure and a heteroatom (silicon, magnesium, scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, gallium, germanium, zirconium, niobium, molybdenum, cadmium, indium, tin, lanthanum or cerium) aluminum phosphate molecular sieve confirmed by the International Zeolite Association. The synthesis method adopts a concentrated glue hydrothermal method, takes low-amount simple quaternary ammonium cations as a template agent, and comprises the following specific synthesis steps: uniformly mixing a phosphorus source, an aluminum source, a heteroatom source (added when a heteroatom aluminophosphate molecular sieve is synthesized), the quaternary ammonium template agent and a fluorine source to obtain an initial reaction mixture; and crystallizing the initial reaction mixture in a closed reactor at a certain temperature for a certain time, and filtering, washing and drying the crystallized product to obtain the aluminum phosphate or heteroatom aluminum phosphate molecular sieve raw powder with the-CLO structure. The synthesis method has the advantages of simple synthesis process, high yield, low synthesis cost, environmental friendliness and the like.

Description

technical field [0001] The invention relates to a method for synthesizing aluminum phosphate and heteroatom aluminum phosphate ultra-large pore molecular sieves, more specifically a method for synthesizing aluminum phosphate and heteroatoms with a -CLO structure by adopting a concentrated glue hydrothermal method and using a low amount of simple quaternary ammonium cation as a template agent. Atomic aluminum phosphate ultra-large pore molecular sieve method. Background technique [0002] Molecular sieve is a crystalline porous material with regular channels and unique surface properties, so it is widely used in chemical fields such as ion exchange, catalysis, adsorption, and separation. The pore size of molecular sieves is an important factor affecting the performance of molecular sieves. The pore sizes of molecular sieve materials that have been industrially applied are all less than 0.75nm, which greatly limits their ability to process large-sized reactant molecules. In or...

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
IPC IPC(8): C01B37/04C01B37/06C01B37/08C01B39/38
CPCC01B37/04C01B37/06C01B37/08C01B37/065C01P2002/72
Inventor 魏莹黄鹏飞张润铎贾静波王昊
Owner BEIJING UNIV OF CHEM TECH