Preparation of quaternary ammonium thiomolybdates

• US 4,343,747 A
• Filed: 12/05/1980
• Issued: 08/10/1982
• Est. Priority Date: 12/05/1980
• Status: Expired due to Term

• Current Assignee: Chevron Research Company (Chevron Corp.)
• Original Assignee: Gulf Research & Development Company
• Inventors: Anglin, James R., Singerman, Gary M., Ryu, Yumi P.
• Primary Examiner(s): SNEED, HELEN
• Application Number:
  US06/213,676
• Time in Patent Office: 613 Days
• Field of Search: 260/429 R
• US Class Current: 556/57
• CPC Class Codes: C07F 11/005 compounds without a metal-carbon linkage
• CPC Class Codes: C10M 2215/02 Amines, e.g. polyalkylene polyamines; Quaternary amines polyalkylene polyamines with eleven or more monomer units C10M2217/046
• CPC Class Codes: C10M 2215/04 having amino groups bound to acyclic or cycloaliphatic carbon atoms
• CPC Class Codes: C10M 2215/042 containing hydroxy groups; Alkoxylated derivatives thereof
• CPC Class Codes: C10M 2215/22 Heterocyclic nitrogen compounds
• CPC Class Codes: C10M 2215/221 Six-membered rings containing nitrogen and carbon only
• CPC Class Codes: C10M 2215/225 the rings containing both nitrogen and oxygen
• CPC Class Codes: C10M 2215/226 Morpholines
• CPC Class Codes: C10M 2215/26 Amines
• CPC Class Codes: C10M 2215/28 Amides; Imides
• CPC Class Codes: C10M 2215/30 Heterocyclic compounds
• CPC Class Codes: C10M 2223/045 Metal containing thio derivatives
• CPC Class Codes: C10N 2010/04 Groups 2 or 12
• CPC Class Codes: C10N 2010/12 Groups 6 or 16

Abstract

Quaternary ammonium thiomolybdates are prepared in a two-phase reaction system by contacting an aqueous solution of a thiomolybdate salt with a solution of a quaternary ammonium salt in a water-immiscible organic solvent. For example, mixing a solution of dicocodimethylammonium chloride in toluene with an aqueous solution of potassium thiomolybdate results in a toluene solution containing dicocodimethylammonium thiomolybdate.

Claims

1. The method of making quaternary ammonium thiomolybdates in a two-phase reaction system which comprises contacting an aqueous solution of a water-soluble thiomolybdate salt with a solution of a quaternary ammonium salt having the formula ##STR3## where R₁, R₂ and R₃ are independently selected from alkyl or alkenyl having from one to about 30 carbon atoms;

R₄ is selected from alkyl or alkenyl having from about 5 to about 30 carbon atoms, and benzyl;

the total number of carbon atoms in R₁, R₂, R₃ and R₄ is between about 20 and about 80;

n is the valence of X; and

X is selected from chlorine, bromine, iodine, sulfate, hydrogen sulfate and lower alkyl sulfate;

in a water-immiscible organic solvent selected from aliphatic hydrocarbons having from about five to about 20 carbon atoms, halogenated aliphatic hydrocarbons having from about one to about two carbon atoms, aromatic hydrocarbons and halogenated aromatic hydrocarbons having from six to about eight carbon atoms, alkyl esters of aliphatic carboxylic acids having from about four to about seven carbon atoms, aliphatic ketones having from about five to about ten carbon atoms, alkyl ethers having from about four to about eight carbon atoms, and mixtures thereof;

wherein the solubility of said quaternary ammonium salt in said organic solvent is at least about five times its solubility in water; and

recovering the quaternary ammonium thiomolybdate produced thereby in the said organic solvent and the by-product salt in the aqueous solution.

2. The method of making quaternary ammonium thiomolybdates in accordance with claim 1 wherein R₁, R₂ and R₃ have from one to about 20 carbon atoms, R₄ has from about 12 to about 20 carbon atoms, and the total number of carbon atoms in R₁, R₂, R₃ and R₄ is between about 25 and about 60.

3. The method of making quaternary ammonium thiomolybdates in accordance with claim 1 wherein the water-soluble thiomolybdate salt is selected from lithium, sodium, potassium, rubidium, cesium, thallium and ammonium thiomolybdate.

4. The method of making quaternary ammonium thiomolybdates in accordance with claim 2 wherein R₁, R₂, R₃ and R₄ are the same.

5. The method of making quaternary ammonium thiomolybdates in accordance with claim 2 wherein R₁ and R₂ are methyl and R₃ has from about 12 to about 20 carbon atoms.

6. The method of making quaternary ammonium thiomolybdates in accordance with claim 2 wherein R₁ is methyl and R₂ and R₃ have from about 12 to about 20 carbon atoms.

7. The method of making quaternary ammonium thiomolybdates in accordance with claim 2 wherein said quaternary ammonium salt is essentially insoluble in water.

8. The method of making quaternary ammonium thiomolybdates in accordance with claim 1 wherein the ratio of the quaternary ammonium salt to the water-soluble thiomolybdate salt is between a mol ratio of about 2:

1 and about a ten percent stoichiometric excess of the water-soluble thiomolybdate salt.

9. The method of making quaternary ammonium thiomolybdates in accordance with claim 1 wherein the solubility of said quaternary ammonium salt in said organic solvent is at least about ten times its solubility in water.

10. The method of making quaternary ammonium thiomolybdates in accordance with claim 1 wherein said product quaternary ammonium thiomolybdate is recovered substantially free of water and by-product salt.