CN1342607A - Process for synthesizing mesoporous SiO2 melecular sieve with cubic structure - Google Patents

Process for synthesizing mesoporous SiO2 melecular sieve with cubic structure Download PDF

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CN1342607A
CN1342607A CN 01126540 CN01126540A CN1342607A CN 1342607 A CN1342607 A CN 1342607A CN 01126540 CN01126540 CN 01126540 CN 01126540 A CN01126540 A CN 01126540A CN 1342607 A CN1342607 A CN 1342607A
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molecular sieve
mesoporous silica
synthetic method
ammonium salt
silica molecular
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CN1142094C (en
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沈绍典
李裕琦
孙锦玉
屠波
赵东元
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Fudan University
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Fudan University
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Abstract

A mesoporous SiO2 as molecular sieve with novel cubic structure is synthesized in alkaline condition by using tri-quaterrary ammonium salt cationic surfactant as structure guide agent. It has 3-D cubic structure (its space group is Fd3m), great specific surface area (about 1000 sq.m/g) and uniform pore diameter.

Description

A kind of synthetic method of mesoporous SiO 2 melecular sieve with cubic structure
Technical field
The invention belongs to inorganic molecule sieve technical field, particularly a kind of spacer is the synthetic method of the novel cube of phase structure mesoporous silica molecular sieve of Fd3m.
Technical background
Meso-porous molecular sieve material be meant with the tensio-active agent be the class aperture that forms of the supramolecule template colloidal sol-gel molecular self-assembly by inorganic species under certain condition between 2-30nm, the inorganic porous material of compound with regular structure.Compare with traditional micro porous molecular sieve, because meso-porous molecular sieve material has characteristics such as meticulous adjustable, the duct long-range order in big and pore size distribution, the aperture of homogeneous, specific surface height, good relatively thermostability and hydrothermal stability, gets more and more people's extensive concerning.Utilize its property, people to it absorption with separate, the assembling of functional materialss such as catalyzer and carrier, light, electricity, magnetic, the fields such as preparation of nano material launched applied research widely.Since the scientist of Mobil in 1992 synthesizes M41S series mesopore molecular sieve (MCM-41, MCM-48 and MCM-50), the scientist of various countries is to the synthetic broad research of having carried out of the mesoporous material of novel texture, synthesized mesopore molecular sieve with different structure in succession as HMS, SBA, MSU series molecular sieve.The mesopore molecular sieve of three-dimensional cubic structure wherein, owing to have three-dimensional network pore passage structure, big specific surface can not only be provided, and under the blocked situation in part duct, can also provide the reaction active site of high passability in the pore network structure, thereby the MCM-41 of the one dimension system of stopping up easily with the duct compares, and the more applications performance is arranged.Up to the present, people have synthesized multiple SiO 2 molecular sieve such as MCM-48 (spacer Ia3d), SBA-16 (spacer Im3m), SBA-1 (spacer Pm3n) etc. with different spaces group cubic structure.But the spacer that has of the cubic liquid crystal structure that last is prone to is that the cubic structure molecular sieve of Fd3m fails to synthesize so far.
Summary of the invention
The purpose of this invention is to provide a kind of spacer is the synthetic method of the novel cube of phase structure mesoporous silica molecular sieve of Fd3m.
The synthetic method of novel cube of phase structure (Fd3m) mesoporous silica molecular sieve that the present invention proposes, with three quaternary ammonium salt cationic tensio-active agents is structure directing agent, synthetic under alkaline condition, its step is as follows: at first be with 0.1-1.0: 800-2000: 2.6-7.2: the 3.0-5.0 mixing in molar ratio of cats product, water, alkali source and silicon source, at room temperature stir for some time, generally can be 1-5 hour, dry down through filtration, washing, air then, 500-550 ℃ roasting temperature 3-5 hour.
In the above-mentioned synthetic method, cats product is selected from three quaternary ammonium salt cationics from tetradecyl to the eicosyl hydrophobic chain.Its chemical structural formula is [C nH 2n+1N +(CH 3) 2-(CH 2) m-N +(CH 3) 2-(CH 2) 1-N +(CN 3) 33Br -], (n=14-20, m=2-6 1=2-6), have three positive charges in its individual molecule, hydrophobic chain is the hydrocarbon chain of 13-19 methylene radical of band.The silicon source is selected from a kind of or its mixture in methyl silicate, tetraethoxy, butyl silicate or water glass, water glass, the white carbon black.Alkali source is selected from sodium hydroxide, potassium hydroxide, cesium hydroxide, tetramethyl ammonium hydroxide solution or its mixture.Temperature of reaction is a room temperature, is generally 13-23 ℃ better.
The key of present technique is to adopt cats product with three quaternary amines and the basicity when synthetic, forms MCM-41 when basicity is too big easily, and basicity hour generates very much amorphous gel easily.
Synthetic general main dependence cats product hydrophilic radical based on mesopore molecular sieve carries out self-assembly and common assembling with the driving of the interface interaction power of coupling of the electric density between the inorganic silicon species polymerization negatively charged ion and organic-inorganic.Therefore to adopt the cats product that has a plurality of electric charges in building-up process be the supramolecule template in the present invention, it helps to improve the organic surface active agent hydrophilic radical with the electrostatic attraction between the inorganic anion species, thereby strengthen the interface interaction power of organic-inorganic, the carrying out that helps the organic-inorganic self-assembly and assemble altogether, and then synthesize silica mesoporous zeolite (FDU-2) with novel cubic structure (Fd3m).The synthetic product that obtains be verified as through XRD and TEM have the novel three-dimensional cubic structure, spacer is the silica mesoporous zeolite of Fd3m.The aperture homogeneous of this molecular sieve is 2.0-4.0nm, can change by the hydrophobic chain length of reconciliation statement surface-active agent; Specific surface area is 500-1500m 2/ g; Pore volume is 0.8-1.0cm 3About/g.
Description of drawings
Fig. 1 is the XRD spectra before the spacer Fd3m cubic structure mesoporous silica molecular sieve material calcination.
Fig. 2 is the XRD spectra behind the spacer Fd3m cubic structure mesoporous silica molecular sieve material calcination.
Fig. 3 is spacer Fd3m cubic structure mesoporous silica molecular sieve material N 2Absorption-desorption isotherm and graph of pore diameter distribution.
Fig. 4 is transmission electron microscope (TEM) picture of spacer Fd3m cubic structure mesoporous silica molecular sieve material, and wherein (a) is [001] face, (b) is [111] face.
Embodiment
Below by embodiment the present invention is further described:
Embodiment 1, with 3g CH 3(CH 2) 16CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 120g water, add 48g 0.5MolL -1Sodium hydroxide solution, the back that stirs adds 8g TEOS (tetraethoxy), the mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, sodium hydroxide and tetraethoxys is: 0.11: 241.6: 0.625: 1.Temperature of reaction is 18 ℃.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 500 ℃ of following roastings 4 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.Sample is made TEM (transmission electron microscope) to be observed.XRD spectra and TEM photo are seen Fig. 1-Fig. 4.The unit cell parameters of calculating product according to the d value on the XRD is a=7.45nm, is consistent with the unit cell parameters a=7.36nm that records on the TEM.N 2Absorption--it is 991m that desorption method records the BET surface-area 2g -1, the BJH aperture is 2.9nm, pore volume is 0.98cm 3.g -1
Embodiment 2, synthesis temperature be 18 ℃ with 12g CH 3(CH 2) 16CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 370g water, add 29g 0.5MolL -1Potassium hydroxide solution, the back that stirs adds 20g TEOS (tetraethoxy), the mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, NaOH and TEOS is: 0.176: 230: 0.152: 1.0.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 50 ℃ of following roastings 3.5 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.36nm, and the BET surface-area is 901m 2g -1, the BJH aperture is 2.4nm, pore volume is 1.03cm 3.g -1
Embodiment 3, synthesis temperature be 20 ℃ with 2.485g CH 3(CH 2) 16CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 1500g water, add the 660g aqueous solution of 2.24g potassium hydroxide, the back that stirs adds 83.3g TEOS.The mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, KOH and TEOS is: 0.088: 300: 1.0: 1.0.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 500 ℃ of following roastings 4 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.73nm, and the BET surface-area of product is 951m 2g -1, the BJH aperture is 2.7nm, pore volume is 0.90cm 3.g -1
Embodiment 4, are with 3g CH under 20 ℃ at synthesis temperature 3(CH 2) 16CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 120g water, add 48.0g0.5MolL -1NaOH solution, the back that stirs adds 12.3g TBOS, the mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, NaOH and TBOS is: 0.11: 241.6: 0.625: 1.After the continuously stirring 1 hour, mixture is filtered, deionized water wash is to neutral, and dry back was in 500 ℃ of following roastings 4.5 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.29nm, and the BET surface-area is 1000m 2g -1, the BJH aperture is 3.2nm, pore volume is 0.95cm 3.g -1
Embodiment 5, are with 23.2g CH under 20 ℃ at synthesis temperature 3(CH 2) 12CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 1500g water, add the 660g aqueous solution of 22.4g KOH, the back that stirs adds 83.3g TEOS.The mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, NaOH and TEOS is: 0.088: 300: 1.0: 1.0.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 500 ℃ of following roastings 4 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.03nm, and the BET surface-area is 912m 2g -1, the BJH aperture is 2.4nm, pore volume is 0.90cm 3.g -1
Embodiment 6, are with 21.3g CH under 20 ℃ at synthesis temperature 3(CH 2) 12CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 2000g water, add the 340g aqueous solution that contains 12.8g NaOH, the back that stirs adds 53.2g TMOS (methyl silicate).The mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, NaOH and TMOS is: 0.3: 1300: 3.2: 3.5.After the continuously stirring 2 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 550 ℃ of following roastings 4 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.26nm, and the BET surface-area is 995m 2g -1, the BJH aperture is 2.8nm, pore volume is 0.94cm 3.g -1
Embodiment 7, are with 20.6g CH under 15 ℃ at synthesis temperature 3(CH 2) 14CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 2000g water, add the 340g aqueous solution that contains 12.8g NaOH, the back that stirs adds 72.9g TEOS.The mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, NaOH and TEOS is: 0.3: 1300: 3.2: 3.5.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 550 ℃ of following roastings 3 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.26nm, and the BET surface-area is 995m 2g -1, the BJH aperture is 2.8nm, pore volume is 0.94cm 3.g -1
Embodiment 8, are with 36.7g CH under 23 ℃ at synthesis temperature 3(CH 2) 18CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2N +CH 2CH 2CH 2(CH 3) 33Br -Be dissolved in the 1500g water, add the 660g aqueous solution that contains 16.4g NaOH, the back that stirs adds 83.3g TEOS (tetraethoxy).The mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, NaOH and TEOS is: 0.5: 1200: 4.1: 4.0.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 500 ℃ of following roastings 4 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.26nm, and the BET surface-area is 995m 2g -1, the BJH aperture is 2.8nm, pore volume is 0.94cm 3.g -1
Embodiment 9, synthesis temperature be 20 ℃ with 3.2g CH 3(CH 2) 16CH 2N +(CH 3) 2CH 2CH 2N +(CH 3) 2CH 2CH 2CH 2N +(CH 3) 33Br -Be dissolved in the 175.7g water, the tetramethyl ammonium hydroxide solution that adds 9.3g 25%, add 13.1g TBOS (butyl silicate) after stirring, the mol ratio of three quaternary ammonium salt cationic tensio-active agents, water, Tetramethylammonium hydroxide and TBOS is: 0.11: 241.6: 0.625: 1.After the continuously stirring 3 hours, mixture is filtered, deionized water wash is to neutral, and dry back was in 500 ℃ of following roastings 4 hours under the room temperature.Measure the position of its diffraction peak 2 θ with XRD (X-ray diffraction), the positioning indexization of diffraction peak 2 θ is confirmed as Fd3m cube of phase structure.The unit cell parameters of calculating product according to the d value on the XRD is a=7.29nm, and the BET surface-area is 1000m 2g -1, the BJH aperture is 3.2nm, pore volume is 0.95cm 3.g -1

Claims (5)

1, a kind of spacer is the synthetic method of the cubic structure mesoporous silica molecular sieve of Fd3m, with three quaternary ammonium salt cationic tensio-active agents is structure directing agent, synthetic under alkaline condition, its concrete steps are: at first be with 0.1-1.0: 800-2000: 2.6-7.2: the 3.0-5.0 mixing in molar ratio of cats product, water, alkali source and silicon source, at room temperature stir for some time; Then through dry under filtration, washing, the air, and in 500-550 ℃ of roasting temperature 3-5 hour.
2, the synthetic method of mesoporous silica molecular sieve according to claim 1 is characterized in that three used quaternary ammonium salt cationic tensio-active agents are three quaternary ammonium salt cationics from tetradecyl to the eicosyl hydrophobic chain.
3, the synthetic method of mesoporous silica molecular sieve according to claim 1 is characterized in that the silicon source is a kind of or its mixture of tetraethoxy, methyl silicate, butyl silicate, water glass, water glass or white carbon black.
4, the synthetic method of mesoporous silica molecular sieve according to claim 1 is characterized in that alkali source is sodium hydroxide, potassium hydroxide, lithium hydroxide, cesium hydroxide or tetramethyl ammonium hydroxide solution or its mixture.
5, the synthetic method of mesoporous silica molecular sieve according to claim 1 is characterized in that synthesis temperature is 10-23 ℃.
CNB01126540XA 2001-08-24 2001-08-24 Process for synthesizing mesoporous SiO2 melecular sieve with cubic structure Expired - Fee Related CN1142094C (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100406380C (en) * 2006-08-04 2008-07-30 华东师范大学 Method of synthesizing ordered mesoporous silica dioxide using cation alkyl glycoside as template agent
CN100420628C (en) * 2003-06-27 2008-09-24 鲁汶天主教大学研究开发部 Crystalline mesoporous oxide based materials useful for the fixation and controlled release of drugs
CN102616795A (en) * 2012-04-23 2012-08-01 华东师范大学 Method for preparing pure silicon-based mesoporous silica nanoparticles
CN102774844A (en) * 2012-08-03 2012-11-14 西安文理学院 Method for preparing dual acid type ordered cage mesoporous silica
CN103058206A (en) * 2012-12-18 2013-04-24 泰山医学院 Method for synthesizing highly ordered super-microporous silicon dioxide

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100420628C (en) * 2003-06-27 2008-09-24 鲁汶天主教大学研究开发部 Crystalline mesoporous oxide based materials useful for the fixation and controlled release of drugs
CN100406380C (en) * 2006-08-04 2008-07-30 华东师范大学 Method of synthesizing ordered mesoporous silica dioxide using cation alkyl glycoside as template agent
CN102616795A (en) * 2012-04-23 2012-08-01 华东师范大学 Method for preparing pure silicon-based mesoporous silica nanoparticles
CN102774844A (en) * 2012-08-03 2012-11-14 西安文理学院 Method for preparing dual acid type ordered cage mesoporous silica
CN102774844B (en) * 2012-08-03 2015-04-15 西安文理学院 Method for preparing dual acid type ordered cage mesoporous silica
CN103058206A (en) * 2012-12-18 2013-04-24 泰山医学院 Method for synthesizing highly ordered super-microporous silicon dioxide

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