CN1500728A - Process for preparing titanium silicon molecular sieves - Google Patents
Process for preparing titanium silicon molecular sieves Download PDFInfo
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- CN1500728A CN1500728A CNA021452415A CN02145241A CN1500728A CN 1500728 A CN1500728 A CN 1500728A CN A021452415 A CNA021452415 A CN A021452415A CN 02145241 A CN02145241 A CN 02145241A CN 1500728 A CN1500728 A CN 1500728A
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- hts
- sio
- described method
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- complex compound
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Abstract
The present invention relates to the preparation process of Ti-Si molecular sieve and solves the problems in the preparation process, including long Ti-Si molecular sieve synthesizing period and the trouble of evaporating alcohol before crystallization. The technological scheme of the present invention is that Ti-Si molecular sieve is hydrothermally synthesized by using organic ammonium and/or amine as template agent, adding acetylacetone, EDTA or N, N-dimethyl amide into the molecular sieve synthesizing material. The present invention may be used in industrial process of preparing Ti-Si molecular sieve.
Description
Technical field
The present invention relates to a kind of method for preparing HTS.
Background technology
HTS has very high catalytic activity and selectivity to the low-carbon (LC) oxidation operation: be oxygenant with the hydrogen peroxide, in temperature is under 40～100 ℃ of conditions, but the reactions such as ammonia oxidation of the hydroxylation of the partial oxidation of the epoxidation of catalyzed alkene, alkane, aromatic hydrocarbon and phenol and pimelinketone.The synthetic method of HTS generally has two kinds: a kind of is to be the titanium source with tetraethyl titanate or tetrabutyl titanate, and tetraethyl orthosilicate is the silicon source, is template with TPAOH TPAOH or TBAH TBAOH, utilizes hydrothermal method synthetic.Wherein the mol ratio of reaction mass is SiO
2/ TiO
2＞30; TPAOH or TBAOH/SiO
2=0.3～0.6.It is the method for the synthetic TS-1 HTS of template with TPAOH that U.S. Pat 04410501 has been introduced.Utilize aforesaid method to synthesize its complicated operating process of TS-1, long reaction time (6～30 days), and be difficult to avoid the tetraethyl titanate hydrolysis and be polymerized to non-body phase anatase.Document BE1001038 (1989) has introduced a kind of method of synthetic TS-2 HTS, and it is to be the titanium source with the tetraethyl titanate, and tetraethyl orthosilicate is the silicon source, is template with the TBAH, utilizes hydrothermal method to synthesize the TS-2 HTS.There is following shortcoming equally in this synthetic method: complicated operating process, long reaction time needs 6～30 days, and is difficult to avoid the tetraethyl titanate hydrolysis and is polymerized to non-body phase anatase TiO
2In addition in the synthesis of titanium silicon molecular sieve process, general earlier titanium being dissolved in the Virahol, and then add the silicon source, but the alcohol that added before crystallization must evaporate, otherwise can reduce the degree of crystallinity of molecular sieve and the order of structure, complicated operation.
Summary of the invention
Technical problem to be solved by this invention is to overcome to exist the HTS generated time long and pure owing to adding in the above-mentioned document, it must be evaporated before the crystallization, and the problem of troublesome poeration provides a kind of new method for preparing HTS.It is short that this method has the synthesis of titanium silicon molecular sieve reaction times, must not add alcohol, convenience operation before the crystallization.
For solving the problems of the technologies described above, the technical solution used in the present invention is as follows: a kind of method for preparing HTS, HTS has following general formula: xTiO
2(1-x) SiO
2, x=0.0005～0.04, wherein x is a mol ratio, x=Ti/ (Si+Ti); It is to be the titanium source with the tetrabutyl titanate, with tetraethyl orthosilicate or silicon sol is the silicon source, quaternary ammonium hydroxide is or/and organic amine is template RN, in building-up process, add and be selected from methyl ethyl diketone, EDTA, N, at least a complex compound in the N-dimethylformamide, wherein the mol ratio of each material is in the molecular sieve precursor: SiO
2/ TiO
2=20～200, OH
-/ SiO
2=0.03～0.6, RN/SiO
2=0.2～0.5, H
2O/SiO
2=60～100, complex compound/TiO
2=0.05～1.5, above-mentioned reaction mixture is 150～200 ℃ at crystallization temperature, and crystallization time is after 4～20 hours, and the fractional crystallization product gets HTS through washing, drying, roasting.
In the technique scheme, in the HTS preparation process, the value preferable range of x is 0.005～0.025; The quaternary ammonium hydroxide preferred version is for being selected from TPAOH, TBAH, tetraethyl ammonium hydroxide or Tetramethylammonium hydroxide; The organic amine preferred version is the diamines of selecting oneself, diethylamine, quadrol, triethylamine or n-Butyl Amine 99.The crystallization temperature preferable range is 150～180 ℃, and the crystallization time preferable range is 5～10 hours.The complex compound preferred version is a methyl ethyl diketone, with molar ratio computing complex compound/TiO
2Be 0.1～0.6.
The present invention is by adding the technical scheme of complex compound in the HTS building-up process, shortened generated time greatly, make generated time shorten to 4～20 hours from the past 6～30 days, the reason inventor wherein still can not explain at present, but generated time prolongs the present invention there is not harm, therefore crystallization time is not limited in 4～20 hours among the present invention, in addition owing to add complex compound in the HTS building-up process, therefore the titanium source need not to be dissolved in the alcohol, saved the trouble of steaming alcohol, easy and simple to handle, obtained effect preferably.
The present invention is further elaborated below by embodiment.
Embodiment
[comparative example 1]
The mixing solutions that the TPAOH (TPAOH) of 20.8 gram positive tetraethyl orthosilicate, suitable quantity of water and 1/3rd requirements is formed is added in the container of band whipping appts.After at room temperature stirring 0.5 hour, the aqueous isopropanol of dropwise adding tetrabutyl titanate (TBOT) stirred 1 hour, added the TPAOH of residual content.Slowly be heated to 80～95 ℃ then, kept 5 hours, to evaporate the alcohol of adding.Change over to again in 100 milliliters of stainless steel autoclaves that are lined with PTFE and carry out crystallization, 175 ℃ of crystallization temperatures, crystallization time 72 hours.The relative molar content of each component wherein:
SiO
2/ TiO
2=50, TPAOH/SiO
2=0.35, H
2O/SiO
2=45, after crystallization finished, water cooled off fast, and isolates crystallized product, after 120 ℃ of dryings, 550 ℃ of calcinations 6 hours, then got HTS, was determined as the TS-1 HTS through the X-Ray diffraction.
[embodiment 1]
The positive tetraethyl orthosilicate of 156.2 grams, 5.1 gram tetrabutyl titanates and 0.8 gram methyl ethyl diketone are joined in the reactor, stir after 1 hour, slowly drip 2.0 milliliters of TPAOH, after stirring 1 hour, add the TPAOH of residual content.Afterwards, above-mentioned reaction mixture is changed in 1 liter of still carry out crystallization.Crystallization temperature is 175 ℃, crystallization time 5 hours.The relative molar content of each component wherein:
SiO
2/ TiO
2=50, TPAOH/SiO
2=0.35, H
2O/SiO
2=45, OH
-/ SiO
2=0.35, methyl ethyl diketone/TiO
2=0.6,
After crystallization finishes, isolate crystallized product and wash with water; After oven dry under 120 ℃, 550 ℃ of following roastings 6 hours, then get HTS, be determined as the TS-1 HTS through the X-Ray diffraction.
[embodiment 2]
With embodiment 1 operation, change just wherein that crystallization time is 7 hours, methyl ethyl diketone/TiO in the material component
2=0.4, the HTS that obtains is determined as the TS-1 HTS through the X-Ray diffraction.
[embodiment 3]
With embodiment 1 operation, change just wherein that crystallization time is 9 hours, methyl ethyl diketone/TiO during raw material is formed
2=0.2, the HTS that obtains is determined as the TS-1 HTS through the X-Ray diffraction.
[embodiment 4]
With embodiment 1 operation, change just wherein that crystallization time is 20 hours, complex compound was selected from EDTA, EDTA/TiO during raw material was formed
2=1.3, the HTS that obtains is determined as the TS-1 HTS through the X-Ray diffraction.
[embodiment 5]
With embodiment 1 operation, change just wherein that crystallization time is 15 hours, complex compound was selected from N, N-dimethylformamide, N, N-dimethylformamide/TiO during raw material was formed
2=0.8, the HTS that obtains is determined as the TS-1 HTS through the X-Ray diffraction.
Claims (8)
1, a kind of method for preparing HTS, HTS has following general formula: xTiO
2(1-x) SiO
2, x=0.0005～0.04, wherein x is a mol ratio, x=Ti/ (Si+Ti); It is to be the titanium source with the tetrabutyl titanate, with tetraethyl orthosilicate or silicon sol is the silicon source, quaternary ammonium hydroxide is or/and organic amine is template RN, in building-up process, add and be selected from methyl ethyl diketone, EDTA, N, at least a complex compound in the N-dimethylformamide, wherein the mol ratio of each material is in the molecular sieve precursor: SiO
2/ TiO
2=20～200, OH
-/ SiO
2=0.03～0.6, H
2O/SiO
2=60～100, RN/SiO
2=0.2～0.5, complex compound/TiO
2=0.05～1.5, above-mentioned reaction mixture is 150～200 ℃ at crystallization temperature, and after crystallization time was 4～20 hours, the fractional crystallization product got HTS through washing, drying, roasting.
2, according to the described method for preparing HTS of claim 1, the span that it is characterized in that x is 0.005～0.025.
3, according to the described method for preparing HTS of claim 1, it is characterized in that quaternary ammonium hydroxide is selected from TPAOH, TBAH, tetraethyl ammonium hydroxide or Tetramethylammonium hydroxide.
4,, it is characterized in that organic amine select oneself diamines, diethylamine, quadrol, triethylamine or n-Butyl Amine 99 according to the described method for preparing HTS of claim 1.
5,, it is characterized in that crystallization temperature is 150～180 ℃ according to the described method for preparing HTS of claim 1.
6,, it is characterized in that crystallization time is 5～10 hours according to the described method for preparing HTS of claim 1.
7, according to the described method for preparing HTS of claim 1, it is characterized in that complex compound is selected from methyl ethyl diketone.
8, according to the described method for preparing HTS of claim 1, it is characterized in that with molar ratio computing complex compound/TiO
2Be 0.1～0.6.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02145241 CN1207204C (en) | 2002-11-13 | 2002-11-13 | Process for preparing titanium silicon molecular sieves |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02145241 CN1207204C (en) | 2002-11-13 | 2002-11-13 | Process for preparing titanium silicon molecular sieves |
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|---|---|
| CN1500728A true CN1500728A (en) | 2004-06-02 |
| CN1207204C CN1207204C (en) | 2005-06-22 |
Family
ID=34232336
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|---|---|---|---|
| CN 02145241 Expired - Lifetime CN1207204C (en) | 2002-11-13 | 2002-11-13 | Process for preparing titanium silicon molecular sieves |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100351176C (en) * | 2005-08-09 | 2007-11-28 | 华东理工大学 | Method of synthesizing titanium silicon molecular sieve using complexig agent to raise titanium source stability |
| CN102502687A (en) * | 2011-10-18 | 2012-06-20 | 大连理工大学 | Method for greenly synthesizing Ti-Si molecular sieve |
| CN105800637A (en) * | 2016-03-18 | 2016-07-27 | 大连理工大学 | Alcohol-removal-free preparation method for rapidly-synthesized high-framework-titanium-content titanium silicalite molecular sieve |
| CN106082259A (en) * | 2016-06-17 | 2016-11-09 | 齐鲁工业大学 | There is overlength catalytic life HTS and low cost preparation method thereof |
| CN111153414A (en) * | 2020-01-16 | 2020-05-15 | 大连理工大学 | Rapid hydrothermal synthesis method of titanium silicalite TS-1 |
| CN112439449A (en) * | 2019-08-28 | 2021-03-05 | 中国石油化工股份有限公司 | Preparation method of titanium-silicon molecular sieve catalyst for improving tetravalent titanium content in framework structure and catalyst thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106517236A (en) * | 2015-09-15 | 2017-03-22 | 中国石油化工股份有限公司 | Preparation method of titanium silicalite molecular sieve |
-
2002
- 2002-11-13 CN CN 02145241 patent/CN1207204C/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100351176C (en) * | 2005-08-09 | 2007-11-28 | 华东理工大学 | Method of synthesizing titanium silicon molecular sieve using complexig agent to raise titanium source stability |
| CN102502687A (en) * | 2011-10-18 | 2012-06-20 | 大连理工大学 | Method for greenly synthesizing Ti-Si molecular sieve |
| CN102502687B (en) * | 2011-10-18 | 2013-06-05 | 大连理工大学 | Method for greenly synthesizing Ti-Si molecular sieve |
| CN105800637A (en) * | 2016-03-18 | 2016-07-27 | 大连理工大学 | Alcohol-removal-free preparation method for rapidly-synthesized high-framework-titanium-content titanium silicalite molecular sieve |
| CN105800637B (en) * | 2016-03-18 | 2018-03-13 | 大连理工大学 | A kind of release alcohol preparation method of the high skeleton Ti content HTS of Fast back-projection algorithm |
| CN106082259A (en) * | 2016-06-17 | 2016-11-09 | 齐鲁工业大学 | There is overlength catalytic life HTS and low cost preparation method thereof |
| CN112439449A (en) * | 2019-08-28 | 2021-03-05 | 中国石油化工股份有限公司 | Preparation method of titanium-silicon molecular sieve catalyst for improving tetravalent titanium content in framework structure and catalyst thereof |
| CN111153414A (en) * | 2020-01-16 | 2020-05-15 | 大连理工大学 | Rapid hydrothermal synthesis method of titanium silicalite TS-1 |
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| Publication number | Publication date |
|---|---|
| CN1207204C (en) | 2005-06-22 |
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