Patent US4851200A successfully refreshed from Google Patents.
US4851200A
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US
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Method for removing organic residue from as-synthesized zeolites
Assignee: Mobil Oil AS
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Filing: 1988-01-04
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Granted: 1989-07-25
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Expires: 2008-01-04
Abstract
Abstract There is provided a three-step method for removing the residue of an organic directing agent from as-synthesized zeolites. The first step involves contacting the as-synthesized zeolite with an aqueous solution of a fluorosilicate salt such as ammonium fluorosilicate. The second step involves ion-exchanging the zeolite with an alkali metal or alkaline earth metal salt such as KCl. The third step involves calcining the ion-exchanged zeolite. This method is particularly useful for removing the residue of an organic directing agent from ZSM-18.
Inventors
- 👤 Francis X. Ryan
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 14:13
CPC Classifications
C; C01; C01B; C01B33/00; C01B33/20; C01B33/26; C01B33/28; C01B33/2807; C01B33/2876; Y; Y10; Y10S; Y10S502/00; Y10S502/50; Y10S502/502
Claims Analysis
Total Claims: 4
Claim 1
Independent Claim
113 words
A method for removing the residue of an organic directing agent from the as-synthesized form of ZSM-18, said organic directing agent being 1,3,4,6,7,9-hexahydro-2,2,5,5,8,8-hexmethyl-2H-benzo (1,2,-C:-3,4-C':5,6-C") tripyrolium trihydroxide, said method comprising the steps of: (i) contacting said as-synthesized form of ZSM-18 with an aqueous solution of ammonium fluorosilicate, said solution containing at least 0.0075 moles of said ammonium fluorosilicate per 100 grams of said as-synthesized ZSM-18; (ii) contacting said ammonium fluorosilicate contacted ZSM-18 of step (i) with a salt of potassium; (iii) calcining said ZSM-18 of step (ii) at a temperature of at least 250° C. in an atmosphere containing NH 3 ; and (iv) repeating said steps (i), (ii) and (iii) at least once.
Claim 2
Independent Claim
113 words
A method for removing the residue of an organic directing agent from the as-synthesized form of ZSM-18, said organic directing agent being 1,3,4,6,7,9-hexahydro-2,2,5,5,8,8-hexmethyl-2H-benzo (1,2,-C:-3,4-C':5,6-C") tripyrolium trihydroxide, said method comprising the steps of: (i) contacting said as-synthesized form of ZSM-18 with an aqueous solution of ammonium fluorosilicate, said solution containing at least 0.0075 moles of said ammonium fluorosilicate per 100 grams of said as-synthesized ZSM-18; (ii) contacting said ammonium fluorosilicate contacted ZSM-18 of step (i) with a salt of potassium; (iii) calcining said ZSM-18 of step (ii) at a temperature of at least 250° C. in an atmosphere containing NH 3 ; and (iv) repeating said steps (i), (ii) and (iii) at least once.
Claim 3
Independent Claim
315 words
A method for preparing the hydrogen form of ZSM-18 which is essentially free of residual organic directing agent, said method comprising the steps of: (i) forming an aqueous reaction mixture capable of forming ZSM-18, said reaction mixture comprising a directing agent which is 1,3,4,6,7,9-hexahydro-2,2,5,5,8,8-hexamethyl-2H-benzo (1,2,-C:-3,4,-C':5,6-C") tripyrolium trihydroxide, a source of sodium cations, a source of silica and a source of alumina, said reaction mixture having a composition, expressed in terms of mole ratios of T and oxides, as follows: SiO 2 /Al 2 O 3 =5-30 Na 2 O/Al 2 O 3 =0.2-5 H 2 O/Al 2 O 3 =200-1500 T/Al 2 O 3 =1-10 where T is said directing agent; (ii) maintaining said reaction mixture of step (i) under conditions sufficient to form crystals of ZSM-18; (iii) separating said ZSM-18 crystals of step (ii) from the mother liquor of said reaction mixture by filtering said crystals and washing said crystals with water, whereby an as-synthesized form of ZSM-18 is obtained, said as-synthesized ZSM-18 having a residue of said organic directing agent in the pores of said ZSM-18; (iv) contacting said as-synthesized form of ZSM-18 of step (iii) with an aqueous solution of ammonium fluorosilicate, said solution containing at least 0.0075 moles of said ammonium fluorosilicate per 100 grams of said as-synthesized ZSM-18; (v) contacting said ammonium fluorosilicate contacted ZSM-18 of step (iv) with a salt of potassium; (vi) calcining said ZSM-18 of step (v) at a temperature of at least 250° C. in an atmosphere containing NH 3 ; (vii) repeating said steps (i), (ii) and (iii) at least once; (viii) contacting said ZSM-18 of step (vii) with an aqueous solution containing ammonium cations to obtain the ammonium exchanged form of ZSM-18; and (ix) calcining said ammonium form of ZSM-18 of step (viii) under conditions sufficient to evolve NH 3 and to convert the ammonium form of ZSM-18 into the hydrogen form of ZSM-18.
Claim 4
Independent Claim
315 words
A method for preparing the hydrogen form of ZSM-18 which is essentially free of residual organic directing agent, said method comprising the steps of: (i) forming an aqueous reaction mixture capable of forming ZSM-18, said reaction mixture comprising a directing agent which is 1,3,4,6,7,9-hexahydro-2,2,5,5,8,8-hexamethyl-2H-benzo (1,2,-C:-3,4,-C':5,6-C") tripyrolium trihydroxide, a source of sodium cations, a source of silica and a source of alumina, said reaction mixture having a composition, expressed in terms of mole ratios of T and oxides, as follows: SiO 2 /Al 2 O 3 =5-30 Na 2 O/Al 2 O 3 =0.2-5 H 2 O/Al 2 O 3 =200-1500 T/Al 2 O 3 =1-10 where T is said directing agent; (ii) maintaining said reaction mixture of step (i) under conditions sufficient to form crystals of ZSM-18; (iii) separating said ZSM-18 crystals of step (ii) from the mother liquor of said reaction mixture by filtering said crystals and washing said crystals with water, whereby an as-synthesized form of ZSM-18 is obtained, said as-synthesized ZSM-18 having a residue of said organic directing agent in the pores of said ZSM-18; (iv) contacting said as-synthesized form of ZSM-18 of step (iii) with an aqueous solution of ammonium fluorosilicate, said solution containing at least 0.0075 moles of said ammonium fluorosilicate per 100 grams of said as-synthesized ZSM-18; (v) contacting said ammonium fluorosilicate contacted ZSM-18 of step (iv) with a salt of potassium; (vi) calcining said ZSM-18 of step (v) at a temperature of at least 250° C. in an atmosphere containing NH 3 ; (vii) repeating said steps (i), (ii) and (iii) at least once; (viii) contacting said ZSM-18 of step (vii) with an aqueous solution containing ammonium cations to obtain the ammonium exchanged form of ZSM-18; and (ix) calcining said ammonium form of ZSM-18 of step (viii) under conditions sufficient to evolve NH 3 and to convert the ammonium form of ZSM-18 into the hydrogen form of ZSM-18.
References Cited (Backward Citations)
US3508867A
Cited
US3933983A
Cited
US3766093A
Cited
US3878127A
Cited
US3969276A
Cited
US3950495A
Cited
US4503023A
Cited
US4273753A
Cited
JPS5643230A
Cited
US4335020A
Cited
US4477584A
Cited
US4414189A
Cited
US4689137A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1992-07-24 | 1993-01-23 | 1993-07-25 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1996-07-24 | 1997-01-23 | 1997-07-25 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2000-07-24 | 2001-01-23 | 2001-07-25 | $7700.00 | Window Closed / Lapsed |