Regeneration of spent supported metal catalysts
View Patent ↗A method for regenerating spent supported metal catalysts comprising treating the spent catalyst with an organo-metallic complex forming agent having an ionization constant pK 1 of at least 2.5. The catalyst activity is restored to an activity level near to or greater than the fresh catalyst. The regeneration method is particularly useful for regenerating spent palladium catalysts on an alumina support as utilized for the hydrogenation of ethyl anthraquinone (EAQ) in the production of hydrogen peroxide.
1. A method for regenerating a used supported metal catalyst, comprising:
(a) providing a used metal catalyst comprising a support and at least one catalytically active metal comprising metal particle clusters attached to the support;
(b) contacting the used supported metal catalyst with at least one organo-metallic complexing agent having an ionization constant pK 1 of at least about 2.5; and
(c) breaking down the metal particle clusters and relocating the at least one catalytically active metal as smaller metal particles on the support to yield a regenerated supported metal catalyst.
2. The method of claim 1 wherein the catalytically active metal comprises one or more noble metals selected from the group consisting of supported palladium, platinum, rhenium, gold, osmium, iridium, rhodium, ruthenium, and combinations thereof.
3. The method of claim 1 wherein the catalytically active metal comprises one or more metals selected from the group consisting of nickel, copper, iron, cobalt, zinc, silver, chromium, vanadium, titanium, molybdenum, tungsten, manganese, scandium, aluminum, gallium, indium, tin, antimony, lead, bismuth, sodium, potassium, lithium, beryllium, calcium, magnesium, lanthanum, cerium, and combinations thereof.
4. The method of claim 1 wherein said supported metal catalyst further comprises one or more non-metals or semimetals selected from the group consisting of boron, carbon, nitrogen, oxygen, fluorine, phosphorus, silicon, sulfur, chlorine, germanium, arsenic, selenium, bromine, tellurium, iodine, and combinations thereof.
5. The method of claim 1 wherein said support comprises porous and/or nonporous supports selected from the group consisting of alumina, silica, titania, kieselguhr, diatomaceous earth, bentonite, clay, zirconia, magnesia, zeolites, carbon black, activated carbon, graphite, flouridated carbon, organic polymers, metals, metal alloys, and combinations thereof.
6. The method of claim 1 wherein the organo-metallic complexing agent comprises an organic chelating agent.
7. The method of claim 6 wherein said organic chelating agent comprises one or more aliphatic or aromatic mono, di, arid/or tribasic carboxylic acids.
8. The method of claim 7 wherein said aliphatic or aromatic mono, di, and/or tribasic carboxylic acids are selected from the group consisting of glycolic acid, malonic acid, tartaric acid, citric acid, succinic acid, glutaric acid, glycine, salicylic acid, isophthalic acid, 2-aminobenzoic acid, and their salts.
9. The method of claim 6 wherein said organic chelating agent comprises one or more polymers selected from the group consisting of polyacrylates, polymethacrylates, polyvinybenzoates, polyvinylsulfate, polyvinyl sulfonates, polybiphenol carbonates, polybenizimidazoles, polyvinylpyrrolidone, and polypyridines.
10. The method of claim 6 wherein said organic chelating agent comprises one or more of aliphatic or aromatic amino compounds selected from the group consisting of ethylene diamine, propylene diamine, diethylenetriamine, triethylenetetraamine, diethylenetriamine pentaacetic acid (DTPA), N-(hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA), and their salts.
11. The method of claim 6 wherein said organic chelating agent comprises phosphonate compounds including amine tri(methylanephosphonic acid) (ATMP), 1-Hydroxy-1,1-diphosphonic acid (HEDP), diethylenetriamine penta (methylphosphonic) acid, and their salts.
12. The method of claim 1 where said organo-metallic complexing agent comprises one or more of an oligomeric or polymeric chelating agent containing one or more acid groups.
13. The method of claim 1 further comprising cleaning, drying and calcining the used catalyst before contacting the used catalyst with said organo metallic complexing agent.
14. The method of claim 1 wherein (b) is carried out at a temperature in a range of 0-400° C. and a pressure in a range of 0-10 atmospheres.
15. The method of claim 1 wherein (b) is carried out for a time period in a range of 1-8 hours.
16. A method for regenerating a used catalyst having supported metal catalyst particles comprising:
a) calcining the used catalyst in air; and
b) contacting the calcined catalyst from a) with at least one organo-metallic complexing agent, whereby the used catalyst is regenerated to a catalytic activity level in a range of 90-103% compared to fresh catalyst activity.
17. The method of claim 16 further including cleaning the used catalyst by contacting it with a solvent before calcining.
18. The method of claim 17 wherein the used catalyst is cleaned at a temperature in a range of 10-100° C. and a pressure in a range of 1-20 atmospheres for a time sufficient to clean the surface of the supported catalyst particles.
19. The method of claim 16 wherein the used catalyst is calcined in air at a temperature range of 350-500° C. for a time period in a range of 2-10 hours.
20. The method of claim 16 wherein the calcinced catalyst is contacted with at least one organo-metallic complexing agent at a temperature in a range of 20-400° C. and a pressure in a range of 1-5 atmospheres for a time sufficient to regenerate the catalyst.
21. The method of claim 16 wherein the organo-metallic complexing agent has a pK 1 of at least about 2.5.
22. The method of claim 16 wherein the supported metal catalyst particles comprise one or more noble metals selected from the group consisting of palladium, platinum, rhenium, gold, osmium, iridium, rhodium, ruthenium, and combinations thereof.
23. The method of claim 16 wherein said organo-metallic complexing agent is selected from the group consisting of aliphatic and/or aromatic mono, di, and/or tribasic carboxylic acids, polyacrylates, polymethacrylates, polyvinybenzoates, polyvinylsulfate, polyvinyl sulfonates, polybiphenol carbonates, polybenizimidazoles, polyvinylpyrrolidone, polypyridines, ethylene diaminc, propylene diaminc, diethylenetriamine, triethylenetctraamine, diethylenetriamine pentaccetic acid (DTPA), N-Qiydroxyethyl)-ethylenediaminetriacctic acid (HEDTA), amino tri(methylanephosphonic acid) (ATMP), 1-Hydroxy-1,1-diphosphonic acid (HEDP), diethylenetriamine penta (methylphosphonic) acid, their salts, and combinations thereof.
24. The method of claim 16 wherein the metal catalyst particles are attached to a catalyst support selected from the group consisting of alumina, silica, titania, keiselguhr, distomaceous earth, bentonite, clay, zirconia, magnesia, zeolites, carbon black, activated carbon, graphite, fluoridated carbon, organic polymers, metals, metal alloys, and combinations thereof.
25. A method for regenerating a spent supported metal catalyst comprising:
contacting the spent supported metal catalyst with at least one organo-metallic complexing agent having an ionization constant pK 1 of at least about 2.5 under conditions sufficient to regenerate the spent supported metal catalyst,
wherein the organo-metallic complexing agent comprises an organic chelating agent, wherein said organic chelating agent comprises:
(i) one or more aliphatic or aromatic mono, di, and/or tribasic carboxylic acids selected from the group consisting of glycolic acid, malonic acid, tartaric acid, citric acid, succinic acid, glutaric acid, glycine, salicylic acid, isophthalic acid, 2-aminobenzoic acid, and their salts; and/or
(ii) one or more phosphonate compounds including amine tri(methylanephosphonic acid) (ATMP), 1-Hydroxy-1,1-diphosphonic acid (HEDP), diethylenetriamine penta (methylphosphonic) acid, and their salts.