CN1724360A - Process for synthesizing microporous titanium silicon fluorite ETS-10 - Google Patents

Process for synthesizing microporous titanium silicon fluorite ETS-10 Download PDF

Info

Publication number
CN1724360A
CN1724360A CN 200510027074 CN200510027074A CN1724360A CN 1724360 A CN1724360 A CN 1724360A CN 200510027074 CN200510027074 CN 200510027074 CN 200510027074 A CN200510027074 A CN 200510027074A CN 1724360 A CN1724360 A CN 1724360A
Authority
CN
China
Prior art keywords
ets
synthetic
inorganic
fluorite
synthetic method
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 200510027074
Other languages
Chinese (zh)
Other versions
CN1321062C (en
Inventor
岳斌
周琰
江磊
闫世润
贺鹤勇
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fudan University
Original Assignee
Fudan University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fudan University filed Critical Fudan University
Priority to CNB2005100270745A priority Critical patent/CN1321062C/en
Publication of CN1724360A publication Critical patent/CN1724360A/en
Application granted granted Critical
Publication of CN1321062C publication Critical patent/CN1321062C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

A process for synthesizing the milli-porous TiSi zeolite ETS-10 features that the inorganic Ti source and inorganic Si source take part in hydrothermal synthesis reaction in alkaline aqueous solution without organic template, F ions and crystal seeds.

Description

The synthetic method of a kind of microporous titanium silicon fluorite ETS-10
Technical field
The invention belongs to inorganic molecule sieve technical field, be specifically related to the synthetic method of a kind of microporous titanium silicon fluorite ETS-10.
Background technology
ETS-10 is a kind of Ti-Si zeolite with unique microvoid structure, and molecular formula is (NaK) 2Si 5TiO 13Kuznicki in reported first in 1989 synthetic (the US patent 4853202) of this Ti-Si zeolite.Studies show that by the shared mutually perpendicular two groups of one-dimensional long chains formed in summit, this long-chain was wrapped in the middle of the pore passage structure of silicon-oxygen tetrahedron composition by titanium-oxygen octahedra in existence during this was zeolite structured.The skeleton of ETS-10 has ternary, five yuan, seven yuan and twelve-ring, and wherein the micropore size that is made of twelve-ring is about 7.6 * 4.9 (Nature, 1994,367,347).Therefore, the structure of ETS-10 can be regarded as the titanium dioxide long-chain with semiconductor property and is inclusive in the middle of the silicon dioxide skeleton structure, and this makes ETS-10 have the character of a lot of uniquenesses.The ETS-10 skeleton is negativity, and there are sodium, potassium counter cation in the surface, can introduce other metallic cation (US patent 4994191) by ion-exchange.The most noticeable then is that ETS-10 is very fast relatively greater than the organic molecule degraded of its microvoid structure to size, then want slowly for little organic molecule degradation speed, thereby show the selective photocatalysis characteristic, therefore can effectively realize selective photocatalysis (Chem.Commun. to different size size organic molecule, 2001,20,2130), become a class novel photocatalysis material that is getting more and more people's extensive concerning in recent years.
The synthesis step more complicated of ETS-10, synthetic organic formwork agent (Zeolites, 1994,14,697 such as use quaternary ammonium salt, aliphatic amide of needing of ETS-10 in the report greatly; J.Chem.Soc.Chem.Commun., 1994,261; Micopor.Mater., 1996,5,401; Micropor.Mater., 1995,4,195; Micopor.Mesopor.Mater., 2002,56,89; Micropor.Mesopor.Mater., 2004,71,77; Stud.Surf.Sci.Catal., 1997,105,221; Stud.Surf.Sci.Catal., 2004,154,334.).Also there are some research work not report having also can synthesize under the condition of organic formwork agent and obtain ETS-10, but need in the presence of a large amount of fluorions, use TiO 2, TiCl 3, TiCl 4, TiF 4, Ti 2(SO 4) 3As titanium source (US Patent 4853202; US Patent 4938939; Chem.Commun., 1996,10,1105; Chem.Commun., 1996,12,1435; Micropor.Mesopor.Mater., 2001,46,1; Micropor.Mesopor.Mater., 2001,47,285; Micropor.Mesopor.Mater., 2002,56,227; Micropor.Mesopor.Mater., 2000,41,79; Micropor.Mesopor.Mater., 2005,80,263; Langmuir, 2003,19,1977; J.Radioanal.Nucl.Chem., 2003,258,243; J.Catal., 2004,224,107.),, except fluorion, in some reports, also add a certain amount of crystal seed (Naure, 1994,367,347 in order to obtain the ETS-10 of high purity, high-crystallinity; Micropor.Mater., 1995,4,195; Micropor.Mesopor.Mater., 1998,23,253; Micopor.Mesopor.Mater., 2005,79,13; USPatent 5453263.).Also there is research to report under the condition that does not add fluorion, organic formwork agent and kind and uses Ti 2(SO 4) 3, TiCl 3, TiO 2As the synthetic preparation in titanium source ETS-10, but contain titanium dioxide impurity (Micropor.Mesopor.Mater., 2004,67,181 in the product with this understanding; Micopor.Mesopor.Mater., 2004,76,113; Stud.Surf.Sci.Catal., 2004,154,770.).Therefore, people are still continuing the simple and effective ETS-10 synthetic method of research exploration.
Summary of the invention
The object of the present invention is to provide a kind of in the system that does not add organic formwork agent, fluorion and crystal seed the synthetic method of microporous titanium silicon fluorite ETS-10.
The present invention proposes the synthetic method of a kind of micropore titanium-silicon zeolite ETS-10, and it is a raw material with inorganic ti sources, inorganic silicon source and mineral alkali under the condition of not using organic formwork agent, fluorion and crystal seed, and is synthetic under hydrothermal condition.Concrete synthesis step is: at first with sodium hydroxide and potassium hydroxide mineral alkali, inorganic silicon source, inorganic ti sources, hydromassage you than 4.0-5.0: 5.0-6.0: 1.0: 100-150 mixes, and the pH value is adjusted to 10.3-10.6; The reactor of packing into then, 200-230 ℃ hydrothermal treatment consists 24-36 hour; The pressed powder that obtains after filtration, after the washing, drying, oven dry obtains having the Ti-Si zeolite ETS-10 of microvoid structure.
Inorganic ti sources such as titanium tetrachloride, titanous chloride, titanium dioxide etc. in the above-mentioned system, inorganic silicon source such as water glass, oxyethyl group silicon etc., alkaline aqueous solution is the mixing solutions of sodium hydroxide and potassium hydroxide.
In the inventive method, good conditions is:
Under 95-105 ℃, dried after the pressed powder drying that obtains after the hydrothermal treatment consists through 10-13 hour.
The mol ratio of synthetic system sodium hydroxide and potassium hydroxide is 2-2.4.
The silicon source of using is sodium silicate aqueous solution, and the titanium source is a titanium tetrachloride.
The microporous titanium silicon fluorite ETS-10 that synthetic method of the present invention obtains is widely used in the synthetic field of catalysis.
Synthetic product nitrogen absorption of the present invention, 29Si solid state nmr and X-ray powder diffraction characterize, and illustrate that the synthetic micro porous molecular sieve that obtains has the feature structure of ETS-10 and do not have other impurity phase.The about 350m of specific surface 2/ g, pore volume are 0.17cm 3/ g.
The advantage of the inventive method is: (1) synthetic system is in the middle of alkaline aqueous solution, obtains by collosol and gel approach hydro-thermal, and method is simple; (2) the synthetic raw material that uses is an industrial chemicals cheap and easy to get; (3) do not need in the building-up process to use organic formwork agent, fluorion and crystal seed, synthetic system is simple and direct, has reduced cost, thereby uses the directly synthetic microporous titanium silicon fluorite ETS-10 that obtains high purity, high-crystallinity of cheap raw material simply and easily.
Description of drawings
Fig. 1 is inorganic silicon source and TiCl in the building-up process 4The different XRD spectra that add than following synthetic microporous titanium silicon fluorite ETS-10; Fig. 1 (a), (b), (c) mesosilicic acid sodium and TiCl 4Molar ratio is respectively 5.2/1,5.5/1, and 5.8/1.
Fig. 2 is embodiment 1 microporous titanium silicon fluorite ETS-10's 29Si solid-state nuclear magnetic resonance spectrogram.
Fig. 3 is embodiment 2 microporous titanium silicon fluorite ETS-10's 29Si solid-state nuclear magnetic resonance spectrogram.
Fig. 4 is embodiment 3 microporous titanium silicon fluorite ETS-10's 29Si solid-state nuclear magnetic resonance spectrogram.
Embodiment
Embodiment 1:
6.00 gram NaOH and 3.90 gram KOH are dissolved in 8.0mL distilled water, then the solution that obtains are slowly added in the 30.28 gram sodium silicate solutions (service water glass), obtain settled solution A; Under vigorous stirring, with 4.75 gram TiCl 4Slowly add in the 10.0mL distilled water, be anti-TiCl in the adition process 4Hydrolysis is too fast, must keep solution temperature to be lower than 10 ℃ with ice-water bath, obtains faint yellow settled solution B.Under the vigorous stirring, solution B is dropwise added solution A, add back pH value of solution value and be about 11.5, with concentrated hydrochloric acid the pH value is transferred to 10.4-10.5 then, the colloid that obtains is transferred in the water heating kettle of teflon lined, 230 ℃ of crystallization 36 hours, naturally cooling, with the products therefrom suction filtration, distilled water wash, 100 ℃ of oven dry.BET measuring result product specific surface 347.6m 2/ g, pore volume are 0.171cm 3/ g.
Embodiment 2:
6.40 gram NaOH and 4.20 gram KOH are dissolved in 10.0mL distilled water, then the solution that obtains are slowly added in the 32.03 gram sodium silicate solutions (water glass), obtain settled solution A; Under vigorous stirring, with 4.75 gram TiCl 4Slowly add in the 8.0mL distilled water, keep solution temperature to be lower than 10 ℃ with ice-water bath in the adition process, obtain faint yellow settled solution B.Under the vigorous stirring, solution B is dropwise added solution A, add back pH value of solution value and be about 11.5, with concentrated hydrochloric acid the pH value is transferred to 10.4-10.5 then, the colloid that obtains is transferred in the water heating kettle of teflon lined, 200 ℃ of crystallization 24h, naturally cooling, with the products therefrom suction filtration, distilled water wash, 100 ℃ of oven dry.BET measuring result product specific surface 357.1m 2/ g, pore volume are 0.172cm 3/ g.
Embodiment 3:
6.40 gram NaOH and 4.20 gram KOH are dissolved in 10.0mL distilled water, then the solution that obtains are slowly added in the 33.78 gram sodium silicate solutions (water glass), obtain settled solution A; Under vigorous stirring, with 4.75 gram TiCl 4Slowly add in the 10.0mL distilled water, keep solution temperature to be lower than 10 ℃ with ice-water bath in the adition process, obtain faint yellow settled solution B.Under the vigorous stirring, solution B is dropwise added solution A, add back pH value of solution value and be about 11.5, with concentrated hydrochloric acid the pH value is transferred to 10.4-10.5 then, the colloid that obtains is transferred in the water heating kettle of teflon lined, 230 ℃ of crystallization 36h, naturally cooling, with the products therefrom suction filtration, distilled water wash, 100 ℃ of oven dry.BET measuring result product specific surface 364.8m 2/ g, pore volume are 0.180cm 3/ g.

Claims (5)

1. the synthetic method of a microporous titanium silicon fluorite ETS-10, it is characterized in that under the condition of not using organic formwork agent, fluorion and crystal seed, with inorganic ti sources, inorganic silicon source and mineral alkali is raw material, synthetic under hydrothermal condition, concrete synthesis step is: at first with sodium hydroxide and potassium hydroxide mineral alkali, inorganic silicon source, inorganic ti sources, hydromassage you than 4.0-5.0: 5.0-6.0: 1.0: 100-150 mixes, and the pH value is adjusted to 10.3-10.6; The reactor of packing into then, 200-230 ℃ hydrothermal treatment consists 24-36 hour; The pressed powder that obtains after filtration, after the washing, drying, oven dry obtains having the Ti-Si zeolite ETS-10 of microvoid structure.
2. microporous titanium silicon fluorite ETS-10 synthetic method according to claim 1 was dried through 10-13 hour under 95-105 ℃ after the pressed powder drying that it is characterized in that obtaining after the hydrothermal treatment consists.
3. microporous titanium silicon fluorite ETS-10 synthetic method according to claim 1, the mol ratio that it is characterized in that synthetic system sodium hydroxide and potassium hydroxide is 2-2.4.
4. the titanium silicon molecular sieve ETS-4 of microvoid structure according to claim 1-10 synthetic method is characterized in that the silicon source of using is sodium silicate aqueous solution, and the titanium source is a titanium tetrachloride.
5. the microporous titanium silicon fluorite ETS-10 that synthetic method according to claim 1 obtains is in the application in the synthetic field of catalysis.
CNB2005100270745A 2005-06-23 2005-06-23 Process for synthesizing microporous titanium silicon fluorite ETS-10 Expired - Fee Related CN1321062C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100270745A CN1321062C (en) 2005-06-23 2005-06-23 Process for synthesizing microporous titanium silicon fluorite ETS-10

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100270745A CN1321062C (en) 2005-06-23 2005-06-23 Process for synthesizing microporous titanium silicon fluorite ETS-10

Publications (2)

Publication Number Publication Date
CN1724360A true CN1724360A (en) 2006-01-25
CN1321062C CN1321062C (en) 2007-06-13

Family

ID=35924016

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100270745A Expired - Fee Related CN1321062C (en) 2005-06-23 2005-06-23 Process for synthesizing microporous titanium silicon fluorite ETS-10

Country Status (1)

Country Link
CN (1) CN1321062C (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101935052B (en) * 2009-06-30 2012-05-30 中国石油化工股份有限公司 Method for synthesizing titanium silicon zeolite material
CN103073021A (en) * 2013-01-11 2013-05-01 东北大学 Method for preparing titanium silicalite ETS-10 with high-silicon industrial raw material
CN104229819A (en) * 2014-08-15 2014-12-24 温州大学 Synthetic method of strongly-alkaline mesoporous ETS-10 zeolite molecular sieve
CN104725280A (en) * 2015-03-04 2015-06-24 温州大学 Synthesis method of diarylurea compounds
US9382124B2 (en) 2011-12-13 2016-07-05 China University Of Petroleum-Beijing (Cupb) Synthesis method for ETS-10 titanosilicate molecular sieve
CN112320816A (en) * 2020-12-09 2021-02-05 成都理工大学 Low-temperature green synthesis method of NaY molecular sieve with small crystal grains and large specific surface area
CN114350182A (en) * 2021-12-17 2022-04-15 沈阳市津浩科技有限公司 Preparation method of modified zeolite for environment-friendly high-performance interior wall coating

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1207196C (en) * 2001-12-21 2005-06-22 清华大学 Nano grade titanium silicon molecular sieve and its synthesis technology
CN1226187C (en) * 2003-05-30 2005-11-09 中国石油化工股份有限公司 Titanium silicon molecular sieve and synthetic method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101935052B (en) * 2009-06-30 2012-05-30 中国石油化工股份有限公司 Method for synthesizing titanium silicon zeolite material
US9382124B2 (en) 2011-12-13 2016-07-05 China University Of Petroleum-Beijing (Cupb) Synthesis method for ETS-10 titanosilicate molecular sieve
CN103073021A (en) * 2013-01-11 2013-05-01 东北大学 Method for preparing titanium silicalite ETS-10 with high-silicon industrial raw material
CN104229819A (en) * 2014-08-15 2014-12-24 温州大学 Synthetic method of strongly-alkaline mesoporous ETS-10 zeolite molecular sieve
CN104725280A (en) * 2015-03-04 2015-06-24 温州大学 Synthesis method of diarylurea compounds
CN112320816A (en) * 2020-12-09 2021-02-05 成都理工大学 Low-temperature green synthesis method of NaY molecular sieve with small crystal grains and large specific surface area
CN114350182A (en) * 2021-12-17 2022-04-15 沈阳市津浩科技有限公司 Preparation method of modified zeolite for environment-friendly high-performance interior wall coating

Also Published As

Publication number Publication date
CN1321062C (en) 2007-06-13

Similar Documents

Publication Publication Date Title
CN1321062C (en) Process for synthesizing microporous titanium silicon fluorite ETS-10
CN104591216B (en) A kind of ZSM-5 and ZSM-12 composite molecular screen and synthetic method thereof
CN101033070A (en) 4A zeolite synthesized from kaolin by low-temperature alkali fusion method
WO2016078035A1 (en) Active aluminosilicate material and preparation method therefor
KR101098495B1 (en) - Process for the manufacture of catalysts used for producing para-xylene by toluene shape selective alkylation
CN107519933B (en) Y/EU-1/SBA-15/ASA/MOF composite material and preparation method
CN1176018C (en) Method for synthesizing small-grain Y-type molecular sieve
CN102616805A (en) Preparation method of titanium-silicon-aluminum molecular sieve ETAS-10
CN101993092A (en) Method for synthesizing ZSM-5 zeolite
CN101774604B (en) Method for synthesizing zeolite through acidactivation of attapulgite clay
CN1281495C (en) Method for preparing Fe-ZSM-5 zeolite microsphere using kieselguhr as raw material
CN104386707B (en) A kind of synthetic method of super low-Na and high-Si nano-ZSM-5 molecular sieve
CN101962194B (en) Method for preparing ZSM-34 and heteroatomic substitution molecular sieve thereof by direct synthesis method
CN1749161A (en) Hard template synthetic composite hole zeolite molecular sieve and its preparing method
CN103395798A (en) Synthesis method of Ti-Beta molecular sieve
CN105712371A (en) USY-Y composite molecular sieve and preparation method thereof
CN101172616A (en) Method of synthesizing micropore titanium silicon molecular sieve ETS-4
CN112174164A (en) ZSM-5 molecular sieve and preparation method thereof
CN109205636A (en) The preparation method of Y/SAPO-34/ZSM-11/ASA multilevel hole material
CN104098108A (en) Rectangular-morphology ZSM-5 molecular sieve and preparation method thereof
CN103121697A (en) Pure silicon ANA-type zeolite molecular sieve and preparation method thereof
CN1151067C (en) process for preparing cubic mesoporous Si-Al molecular sieve with strong acidic site
Azizi et al. Synthesis of NaA zeolite using PTMAOH (phenyltrimethylammoniumhydroxide): hydrothermal and microwave heating methods and comparison of their XRD patterns
CN1359851A (en) Gas-solid phase isomorphous replacement process for preparing Ti-Si zeolite
CN104591208A (en) X-type zeolite having FAU frame structure and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070613

Termination date: 20100623