RU97117371A - METHOD FOR PRODUCING ZEOLITES WITH AN AVERAGE PORE SIZE USING NEUTRAL AMINES - Google Patents
METHOD FOR PRODUCING ZEOLITES WITH AN AVERAGE PORE SIZE USING NEUTRAL AMINESInfo
- Publication number
- RU97117371A RU97117371A RU97117371/25A RU97117371A RU97117371A RU 97117371 A RU97117371 A RU 97117371A RU 97117371/25 A RU97117371/25 A RU 97117371/25A RU 97117371 A RU97117371 A RU 97117371A RU 97117371 A RU97117371 A RU 97117371A
- Authority
- RU
- Russia
- Prior art keywords
- zeolite
- tertiary
- nitrogen
- mixtures
- composition
- Prior art date
Links
- 239000010457 zeolite Substances 0.000 title claims 18
- 150000001412 amines Chemical class 0.000 title claims 11
- 230000001264 neutralization Effects 0.000 title claims 8
- 239000011148 porous material Substances 0.000 title claims 6
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 claims 18
- 125000004432 carbon atoms Chemical group C* 0.000 claims 9
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 150000001768 cations Chemical class 0.000 claims 5
- 150000002829 nitrogen Chemical group 0.000 claims 5
- UAOMVDZJSHZZME-UHFFFAOYSA-N Diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 claims 4
- 239000007864 aqueous solution Substances 0.000 claims 4
- 229910052751 metal Inorganic materials 0.000 claims 4
- 239000002184 metal Substances 0.000 claims 4
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 3
- 125000003277 amino group Chemical group 0.000 claims 3
- 229910052733 gallium Inorganic materials 0.000 claims 3
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims 3
- 229910052732 germanium Inorganic materials 0.000 claims 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims 3
- 229910052738 indium Inorganic materials 0.000 claims 3
- 229910052742 iron Inorganic materials 0.000 claims 3
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims 3
- 229910052710 silicon Inorganic materials 0.000 claims 3
- 239000010703 silicon Substances 0.000 claims 3
- 239000010936 titanium Substances 0.000 claims 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 3
- 229910052719 titanium Inorganic materials 0.000 claims 3
- ZEBFPAXSQXIPNF-UHFFFAOYSA-N 2,5-dimethylpyrrolidine Chemical compound CC1CCC(C)N1 ZEBFPAXSQXIPNF-UHFFFAOYSA-N 0.000 claims 2
- SDGKUVSVPIIUCF-UHFFFAOYSA-N 2,6-Dimethylpiperidine Chemical compound CC1CCCC(C)N1 SDGKUVSVPIIUCF-UHFFFAOYSA-N 0.000 claims 2
- NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-N-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 claims 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N Isobutylamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 claims 2
- BHRZNVHARXXAHW-UHFFFAOYSA-N Sec-Butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 claims 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N Trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims 2
- 229910052782 aluminium Inorganic materials 0.000 claims 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 claims 2
- 229940043279 diisopropylamine Drugs 0.000 claims 2
- 150000002739 metals Chemical class 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims 2
- 102000014961 Protein Precursors Human genes 0.000 claims 1
- 108010078762 Protein Precursors Proteins 0.000 claims 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N al2o3 Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims 1
- -1 alkaline earth metal cation Chemical class 0.000 claims 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims 1
- 125000004429 atoms Chemical group 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 238000005342 ion exchange Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims 1
- 230000000737 periodic Effects 0.000 claims 1
- 229910052761 rare earth metal Inorganic materials 0.000 claims 1
- 150000002910 rare earth metals Chemical class 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
Claims (1)
(а) приготовление водного раствора из (1) источников оксида щелочного металла, оксида щелочноземельного металла или их смесей, (2) источников оксида, выбранного из оксида алюминия, железа, галлия, индия, титана или их смесей, (3) источников оксида, выбранного из оксидов кремния, германия или их смесей, и (4) по крайней мере одного малого нейтрального амина, способного к образованию цеолита, указанный амин содержит (а) только атомы углерода, азота и водорода, (b) одну первичную, вторичную или третичную, но не четвертичную аминогруппу и (с) третичный атом азота, по крайней мере один третичный атом углерода или атом азота, присоединенный непосредственно к по крайней мере одному вторичному атому углерода;
(b) поддерживание водного раствора при условиях, достаточных для образования кристаллов цеолита; и
(с) извлечение кристаллов цеолита, причем способ осуществляют в отсутствии соединения четвертичного аммония.1. The method of producing zeolite with an average pore size, characterized in that it includes:
(a) preparing an aqueous solution of (1) sources of alkali metal oxide, alkaline earth metal oxide or mixtures thereof, (2) sources of oxide selected from aluminum oxide, iron, gallium, indium, titanium or mixtures thereof, (3) oxide sources, selected from oxides of silicon, germanium or mixtures thereof, and (4) at least one small neutral amine capable of forming zeolite, said amine contains (a) only carbon, nitrogen and hydrogen atoms, (b) one primary, secondary or tertiary but not a quaternary amino group and (c) a tertiary atom m nitrogen, at least one tertiary carbon atom or a nitrogen atom bonded directly to at least one secondary carbon atom;
(b) maintaining the aqueous solution under conditions sufficient to form zeolite crystals; and
(c) recovering zeolite crystals, the process being carried out in the absence of a quaternary ammonium compound.
YO2/W2O3 - 15-100
OH-/YO2 - 0,10-0,40
Q/YO2 - 0,05-0,50
М2/n/YO2 - 0,05-0,40
H2O/YO2 - 10-70
где Y представляет кремний, германий или их смеси, W представляет алюминий, галлий, индий, железо, титан или их смеси, Q представляет по крайней мере один малый нейтральный амин, способный к образованию цеолита, указанный амин содержит (а) только атомы углерода, азота и водорода, (b) одну первичную, вторичную или третичную, но не четвертичную аминогруппу и (с) третичный атом азота, по крайней мере один третичный атом углерода или атом азота, присоединенный непосредственно к по крайней мере одному вторичному атому углерода, М представляет щелочной металл, щелочноземельный металл или их смеси, и n представляет валентность компонента М, причем способ осуществляют в отсутствии соединения четвертичного аммония.2. The method according to p. 1, characterized in that said aqueous solution contains the following composition, expressed in molar ratios:
YO 2 / W 2 O 3 - 15-100
OH- / YO 2 - 0.10-0.40
Q / YO 2 - 0.05-0.50
M 2 / n / YO 2 - 0.05-0.40
H 2 O / YO 2 - 10-70
where Y represents silicon, germanium or mixtures thereof, W represents aluminum, gallium, indium, iron, titanium or mixtures thereof, Q represents at least one small neutral amine capable of forming zeolite, said amine contains (a) only carbon atoms, nitrogen and hydrogen, (b) one primary, secondary or tertiary but not quaternary amino group and (c) a tertiary nitrogen atom, at least one tertiary carbon atom or a nitrogen atom attached directly to at least one secondary carbon atom, M represents alkaline metal, alkaline earth metal or mixtures thereof, and n represents the valency of component M, the method being carried out in the absence of a quaternary ammonium compound.
YO2/W2O3 - 25-50
OH-/YO2 - 0,15-0,30
Q/YO2 - 0,10-0,30
M2/n/YO2 - 0,075-0,30
H2O/YO2 - 25-50
4. Способ по п. 1, отличающийся тем, что малый нейтральный амин выбирают из группы, состоящей из изобутиламина, диизобутиламина, триметиламина, циклопентиламина, диизопропиламина, втор-бутиламина, 2,5 - диметилпирролидина и 2,6-диметилпиперидина.3. The method according to p. 2, characterized in that said aqueous solution contains the following composition, expressed in molar ratios:
YO 2 / W 2 O 3 - 25-50
OH- / YO 2 - 0.15-0.30
Q / YO 2 - 0.10-0.30
M 2 / n / YO 2 - 0.075-0.30
H 2 O / YO 2 - 25-50
4. The method according to p. 1, characterized in that the small neutral amine is selected from the group consisting of isobutylamine, diisobutylamine, trimethylamine, cyclopentylamine, diisopropylamine, sec-butylamine, 2,5-dimethylpyrrolidine and 2,6-dimethylpiperidine.
YO2/W2O3 - ≥15
Q/YO2 - 0,02-0,10
M2/n/YO2 - 0,015-0,10
где Y представляет кремний, германий или их смесь, W представляет алюминий, галлий, индий, железо, титан или их смеси, Q представляет по крайней мере один малый нейтральный амин, способный к образованию цеолита, указанный амин содержит (а) только атомы углерода, азота и водорода, (b) одну первичную, вторичную или третичную, но не четвертичную аминогруппу и (с) третичный атом азота, по крайней мере один третичный атом углерода или атом азота, присоединенный непосредственно к по крайней мере одному вторичному атому углерода, М представляет катион щелочного металла, катион щелочноземельного металла или их смеси, и n представляет валентность компонента М, причем указанная композиция не содержит соединения четвертичного аммония.11. The composition of the zeolite with an average pore size, as synthesized and in an anhydrous state, having the following General formula, expressed in molar ratios:
YO 2 / W 2 O 3 - ≥15
Q / YO 2 - 0.02-0.10
M 2 / n / YO 2 - 0.015-0.10
where Y represents silicon, germanium or a mixture thereof, W represents aluminum, gallium, indium, iron, titanium or mixtures thereof, Q represents at least one small neutral amine capable of forming zeolite, said amine contains (a) only carbon atoms, nitrogen and hydrogen, (b) one primary, secondary or tertiary but not quaternary amino group and (c) a tertiary nitrogen atom, at least one tertiary carbon atom or a nitrogen atom attached directly to at least one secondary carbon atom, M represents cation u mammary metal, alkaline earth metal cation or mixtures thereof, and n represents the valence of M component, said composition does not contain a quaternary ammonium compound.
Тета d Отн. I
7.94 11.13 M
8.84 10.00 S
14.79 5.98 W
20.86 4.25 W
23.09 3.85 VS
23.69 3.75 M
14. Композиция цеолита по п. 12, имеющая следующую рентгенограмму:
2Тета d Отн. I
8.15 10.84 VS
10.16 8.70 W
12.77 6.93 W
16.32 5.43 W
19.40 4.57 W
20.34 4.36 VS
24.56 3.62 VS
24.67 3.47 M
35.58 2.52 M
15. Композиция цеолита по п. 12, которая не содержит никакого азотсодержащего органического калибровочного агента, отличного от малого нейтрального амина.13. The composition of the zeolite according to p. 12, having the following x-ray:
Theta d Rel. I
7.94 11.13 M
8.84 10.00 S
14.79 5.98 W
20.86 4.25 W
23.09 3.85 VS
23.69 3.75 M
14. The composition of the zeolite according to p. 12, having the following x-ray:
2 Theta d Rel. I
8.15 10.84 VS
10.16 8.70 W
12.77 6.93 W
16.32 5.43 W
19.40 4.57 W
20.34 4.36 VS
24.56 3.62 VS
24.67 3.47 M
35.58 2.52 M
15. The zeolite composition according to claim 12, which does not contain any nitrogen-containing organic calibration agent other than a small neutral amine.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40608795A | 1995-03-17 | 1995-03-17 | |
US08/406,087 | 1996-03-04 | ||
US08/610,449 US5707600A (en) | 1995-03-17 | 1996-03-04 | Process for preparing medium pore size zeolites using neutral amines |
US08/610,449 | 1996-03-04 | ||
PCT/US1996/003283 WO1996029285A1 (en) | 1995-03-17 | 1996-03-08 | A process for preparing medium pore size zeolites using neutral amines |
Publications (2)
Publication Number | Publication Date |
---|---|
RU97117371A true RU97117371A (en) | 1999-07-20 |
RU2148554C1 RU2148554C1 (en) | 2000-05-10 |
Family
ID=27019374
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU97117371A RU2148554C1 (en) | 1995-03-17 | 1996-03-08 | Method of preparing median pore-size zeolites using neutral amines |
Country Status (9)
Country | Link |
---|---|
US (1) | US5707600A (en) |
EP (2) | EP1110912A3 (en) |
JP (1) | JP4623762B2 (en) |
KR (1) | KR19980702949A (en) |
CN (1) | CN1079371C (en) |
AU (1) | AU5188796A (en) |
DE (1) | DE69626195T2 (en) |
RU (1) | RU2148554C1 (en) |
WO (1) | WO1996029285A1 (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5785947A (en) * | 1991-12-18 | 1998-07-28 | Chevron U.S.A. Inc. | Preparation of zeolites using organic template and amine |
WO1996031434A1 (en) * | 1995-04-03 | 1996-10-10 | Massachusetts Institute Of Technology | Composition and method for producing hexagonally-packed mesoporous metal oxide |
US6616911B2 (en) * | 2000-03-07 | 2003-09-09 | Chevron U.S.A. Inc. | Process for preparing zeolites using pyrrolidinium cations |
FI118516B (en) | 2003-03-14 | 2007-12-14 | Neste Oil Oyj | Process for the preparation of the catalyst |
US7022308B1 (en) * | 2004-09-22 | 2006-04-04 | Chevron U.S.A. Inc. | Preparation of molecular sieve SSZ-33 |
US7157075B1 (en) | 2005-08-30 | 2007-01-02 | Chevron U.S.A. Inc. | Process for preparing MTT zeolites using nitrogen-containing organic compounds |
ITMI20061231A1 (en) * | 2006-06-26 | 2007-12-27 | Eni Spa | PROXCESS AND ZEOLITHIC MATERIALS FOR GAS SEPARATION |
US8007763B2 (en) * | 2006-09-25 | 2011-08-30 | Chevron U.S.A. Inc. | Preparation of molecular sieves using a structure directing agent and an N,N,N-trialkyl benzyl quaternary ammonium cation |
US8057782B2 (en) | 2006-12-27 | 2011-11-15 | Chevron U.S.A. Inc. | Preparation of small pore molecular sieves |
US8007764B2 (en) | 2006-12-27 | 2011-08-30 | Chevron U.S.A. Inc. | Preparation of molecular sieve SSZ-13 |
US7597874B1 (en) | 2008-06-23 | 2009-10-06 | Chevron U.S.A. Inc. | Preparation of zeolites using novel structure directing agents |
EP3055252B1 (en) * | 2013-10-11 | 2017-12-27 | Chevron U.S.A. Inc. | Molecular sieve ssz-96 |
CN106315611A (en) * | 2016-08-24 | 2017-01-11 | 山东齐鲁华信高科有限公司 | SSZ -13 molecular sieve preparing method |
RU2692019C1 (en) * | 2018-07-05 | 2019-06-19 | Кристина Викторовна Тарасенко | Method for concealed fixation of hair |
US11220435B1 (en) | 2021-03-26 | 2022-01-11 | Chevron U.S.A. Inc. | Molecular sieve SSZ-94, catalyst, and methods of use thereof |
BR112023019568A2 (en) * | 2021-03-26 | 2023-12-05 | Chevron Usa Inc | SSZ-93 MOLECULAR SIEVE, CATALYST AND METHODS OF USE THEREOF |
Family Cites Families (26)
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CA1040187A (en) * | 1973-09-07 | 1978-10-10 | Mobil Oil Corporation | Method of preparing a crystalline aluminosilicate zeolite |
CA1064890A (en) * | 1975-06-10 | 1979-10-23 | Mae K. Rubin | Crystalline zeolite, synthesis and use thereof |
US4296083A (en) * | 1977-04-22 | 1981-10-20 | Mobil Oil Corporation | Zeolite synthesis |
NL7812162A (en) * | 1978-12-14 | 1980-06-17 | Shell Int Research | PROCESS FOR THE PREPARATION OF FERRIERITE. |
NL7908984A (en) * | 1979-12-13 | 1981-07-16 | Shell Int Research | PROCESS FOR THE PREPARATION OF CRYSTALLINE SILICATES |
US4377502A (en) * | 1979-12-26 | 1983-03-22 | Standard Oil Company (Indiana) | Synthesis of crystalline aluminosilicate molecular sieves |
US4495166A (en) * | 1982-07-19 | 1985-01-22 | Mobil Oil Corporation | Synthesis of ZSM-5 utilizing a mixture of quaternary ammonium ions and amines |
EP0103981A1 (en) * | 1982-09-03 | 1984-03-28 | Imperial Chemical Industries Plc | Zeolites |
US4481177A (en) * | 1982-12-09 | 1984-11-06 | Mobil Oil Corporation | Synthesis of zeolite ZSM-22 with a heterocyclic organic compound |
US4483835A (en) * | 1983-11-14 | 1984-11-20 | Chevron Research Company | Process for preparing molecular sieves using imidazole template |
JPS6147425A (en) * | 1984-08-10 | 1986-03-07 | Sumitomo Chem Co Ltd | Method of dealkylation selectively in para-position |
US4661467A (en) * | 1985-10-10 | 1987-04-28 | Mobil Oil Corporation | Preparation of catalyst composition comprising a boron containing crystalline material having the structure of zeolites ZSM-5, ZSM-11, ZSM-12, Beta or Nu-1 |
US5063038A (en) * | 1985-10-21 | 1991-11-05 | Mobil Oil Corp. | Zeolite synthesis using an alcohol or like molecule |
GB8612528D0 (en) * | 1986-05-22 | 1986-07-02 | British Petroleum Co Plc | Synthesis of zsm-23 |
US5252527A (en) * | 1988-03-23 | 1993-10-12 | Chevron Research And Technology Company | Zeolite SSZ-32 |
US5053373A (en) * | 1988-03-23 | 1991-10-01 | Chevron Research Company | Zeolite SSZ-32 |
EP0473509A3 (en) * | 1990-08-29 | 1992-03-18 | Rhone-Poulenc Chimie | Method for preparation of zeolites based on silica and, possibly, oxides of tetravalent elements |
RU1799355C (en) * | 1990-10-10 | 1993-02-28 | Грозненский нефтяной научно-исследовательский институт | Method of synthesis nitrogen-containing zeolite of pentasil type making |
US5174977A (en) * | 1991-10-04 | 1992-12-29 | Mobil Oil Corp. | Synthesis of crystalline ZSM-5-type material |
US5174978A (en) * | 1991-10-04 | 1992-12-29 | Mobil Oil Corp. | Synthesis of crystalline ZSM-5-type material |
US5174981A (en) * | 1991-10-04 | 1992-12-29 | Mobil Oil Corp. | Synthesis of crystalline ZSM-5-type material |
US5209918A (en) * | 1991-10-04 | 1993-05-11 | Mobil Oil Corp. | Synthesis of crystalline ZSM-5-type material |
US5173281A (en) * | 1991-10-07 | 1992-12-22 | Mobil Oil Corp. | Synthesis of a synthetic porous crystalline material |
US5190736A (en) * | 1991-10-18 | 1993-03-02 | Mobil Oil Corporation | Synthesis of crystalline ZSM-35 |
US5376260A (en) * | 1993-04-05 | 1994-12-27 | Chevron Research And Technology Company | Process for producing heavy lubricating oil having a low pour point |
DE4323774A1 (en) * | 1993-07-15 | 1995-02-09 | Basf Ag | Hollow ball-like agglomerated pentasil zeolites |
-
1996
- 1996-03-04 US US08/610,449 patent/US5707600A/en not_active Expired - Lifetime
- 1996-03-08 WO PCT/US1996/003283 patent/WO1996029285A1/en active IP Right Grant
- 1996-03-08 KR KR1019970706357A patent/KR19980702949A/en not_active Application Discontinuation
- 1996-03-08 JP JP52845796A patent/JP4623762B2/en not_active Expired - Lifetime
- 1996-03-08 EP EP01100071A patent/EP1110912A3/en not_active Withdrawn
- 1996-03-08 DE DE69626195T patent/DE69626195T2/en not_active Expired - Lifetime
- 1996-03-08 RU RU97117371A patent/RU2148554C1/en active
- 1996-03-08 CN CN96193321A patent/CN1079371C/en not_active Expired - Lifetime
- 1996-03-08 EP EP96908747A patent/EP0815053B1/en not_active Expired - Lifetime
- 1996-03-08 AU AU51887/96A patent/AU5188796A/en not_active Abandoned
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