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Chelated lithium aluminum compounds

Assignee: ExxonMobil Technology and Engineering Co
•
Filing: 1978-02-13
•
Granted: 1979-05-01
•
Expires: 1998-02-13
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Abstract

Abstract Chelated lithium aluminum compounds are prepared by mixing a lithium aluminum compound such as a lithium aluminum hydride with a chelating agent wherein the agent contains at least one nitrogen atom. The chelating agent is a tertiary polyamine or aminoether. The resultant chelate is used for a variety of processes such as separations, catalytic reactions, substitution reactions, reductions, electrochemical reactions, and also as an oil and fuel additive.

Inventors

  • 👤 Arthur W. Langer, Jr.
  • 👤 Thomas A. Whitney

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 16:23
CPC Classifications
C; C07; C07F; C07F9/00; C07F9/02; C07F1/00; C07F1/005; C07F5/00; C07F9/28; C07F9/50; C10; C10L; C10L1/00; C10L1/10; C10L1/14; C10L1/30; C10L1/301; C10M; C10M159/00; C10M159/12; C10M159/18; C10M3/00; C10M2207/00; C10M2207/10; C10M2207/12; C10M2207/125; C10M2207/129; C10M2215/00; C10M2215/02; C10M2215/04; C10M2215/042; C10M2215/044; C10M2215/06; C10M2215/062; C10M2215/064; C10M2215/066; C10M2215/14; C10M2215/22; C10M2215/221; C10M2215/222; C10M2215/225; C10M2215/226; C10M2215/24; C10M2215/26; C10M2215/30; C10M2217/00; C10M2217/04; C10M2217/046; C10M2217/06; C10M2219/00; C10M2219/04; C10M2219/08; C10M2219/082; C10M2219/087; C10M2219/088; C10M2219/089; C10M2223/00; C10M2223/02; C10M2223/049; C10M2223/06; C10M2223/061; C10M2227/00; C10M2227/09; C10N; C10N2010/00; C10N2010/02; C10N2010/04; C10N2010/06

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 247 words
A process for purifying impure commercial mixtures of LiAlH 4 or LiBH 4 , said process comprising the steps of: (a) contacting the impure hydride with a chelating agent selected from the group consisting of sparteine, N,N'-di-(C 1 -C 4 alkyl) bispidins, tris-(β-C 1 -C 4 -di-alkylaminoethyl) amines and those compounds having the formulas: ##STR7## wherein a is 1 or 2, depending on the valence of Y; b is 0 or 1, depending on the valence of Y; C is an integer of 0 to 4 inclusive; e is an integer of 0 to 3 inclusive; R' is the same or different C 1 -C 4 alkyl radical, R" is one selected from the group consisting of C 1 -C 4 alkyl, C 6 -C 10 aryl or aralkyl radical; Y is a nitrogen or oxygenation; Z is a nonreactive radical selected from the group consisting of: (1) C 4 -C 10 cycloaliphatic radicals, or aromatic radicals and their lower alkyl derivatives wherein said radicals are attached to the nitrogen or oxygen atoms in Formula I and the nitrogen atoms in Formula II at 1,2-position on the aromatic rings or 1,2- or 1,3- positions on the cycloaliphatic rings; and (2) 1 to 4 carbon methylenic radicals, wherein each methylenic radical contains 0 to 2 monovalent hydrocarbon radicals of 1 to 6 carbon atoms, in the presence of a solvent for the chelate and (b) separating the soluble chelated LiAlH 4 or LiBH 4 from the insoluble products.
Claim 2
Dependent Claim 247 words
A process for purifying impure commercial mixtures of LiAlH 4 or LiBH 4 , said process comprising the steps of: (a) contacting the impure hydride with a chelating agent selected from the group consisting of sparteine, N,N'-di-(C 1 -C 4 alkyl) bispidins, tris-(β-C 1 -C 4 -di-alkylaminoethyl) amines and those compounds having the formulas: ##STR7## wherein a is 1 or 2, depending on the valence of Y; b is 0 or 1, depending on the valence of Y; C is an integer of 0 to 4 inclusive; e is an integer of 0 to 3 inclusive; R' is the same or different C 1 -C 4 alkyl radical, R" is one selected from the group consisting of C 1 -C 4 alkyl, C 6 -C 10 aryl or aralkyl radical; Y is a nitrogen or oxygenation; Z is a nonreactive radical selected from the group consisting of: (1) C 4 -C 10 cycloaliphatic radicals, or aromatic radicals and their lower alkyl derivatives wherein said radicals are attached to the nitrogen or oxygen atoms in Formula I and the nitrogen atoms in Formula II at 1,2-position on the aromatic rings or 1,2- or 1,3- positions on the cycloaliphatic rings; and (2) 1 to 4 carbon methylenic radicals, wherein each methylenic radical contains 0 to 2 monovalent hydrocarbon radicals of 1 to 6 carbon atoms, in the presence of a solvent for the chelate and (b) separating the soluble chelated LiAlH 4 or LiBH 4 from the insoluble products.
Claim 3
Dependent Claim 30 words
The process of claim 1 further comprising the step of dissociating the separated soluble chelated material of step (b) into pure LiAlH 4 or LiBH 4 and recovered chelating agent.
Claim 4
Dependent Claim 38 words
The process of claim 1 or 2 wherein the chelating agent is selected from the group consisting of tetramethylethylene diamine (TMED), pentamethyl diethylene triamine (PMDT), N,N,N',N'-tetramethyl-1,4-butane diamine (TMBD), N,N,N',N'-tetramethyl-1,2-cyclohexane diamine (TMCHD), tris-(β-di-methylaminoethyl) amine (iso-HMTT), tetramethyl methane diamine (TMMD).
Claim 5
Dependent Claim 11 words
The process of claim 3 wherein the chelating agent is TMED.

References Cited (Backward Citations)

US2729540A Cited
US2656243A Cited
US3107157A Cited
US3734963A Cited
US3933879A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-04-30 1982-10-30 1983-05-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-04-30 1986-10-30 1987-05-01 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-04-30 1990-10-30 1991-05-01 $7700.00 Window Closed / Lapsed

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