Hydroisomerization of pentane utilizing Pd exchanged mordenite
AssigneeNorton Company
InventorsJoseph R. Kiovsky, William J. Goyette
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AssigneeNorton Company
InventorsJoseph R. Kiovsky, William J. Goyette
Estimating the term…
Ammonia exchanged large port mordenite, which is subsequently mildly acid leached, and calcined, in which at least 95% of the exchangeable sodium has been removed and having from 0.38 to 0.8 milliequivalents of acid sites at least as strong as 48% sulfuric acid per gram (as measured by titration with butylamine, and employing dicinnamalacetone indicator) has been found to be highly active hydrocarbon isomerization catalyst. Incorporation of noble metal, e.g. palladium, on the catalyst improves the selectivity for isomerization of normal pentane to isopentane for highly active catalysts at high conversion rates.
A method of isomerizing comprising passing a mixture of hydrogen and pentane over Pd exchanged mordenite at a temperature between 450.degree. F. and 550.degree. F., characterized in that said mordenite contain less than 0.2% by weight exchanged sodium, has a silica to alumina ratio of between 10 and 17, contains from 0.38 to 0.8 milliequivalents per gram of acid sites stronger than 48% aqueous sulfuric acid.
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Containing iron group metals, noble metals or copper: noble metals
Catalytic processes: with metals
Chemical or physical processes
Acyclic or carbocyclic compounds
Term ended 4 Nov 1997 (estimated)
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An improved zeolite catalyst of high acidity for reactions such as the isomerization of normal hydrocarbons, and methods of making and using are taught. Other reactions for which highly acid catalysts are desireable are alkylation and cracking of hydrocarbons.
U.S. Pat. Nos. 3,475,345; 3,324,188; and 3,190,939 teach the use of large port hydrogen exchanged mordenite as a catalyst for hydrocarbon isomerization. The first named patent discloses that strong, hot acid leaching followed by mild acid leaching, finally followed by ammonium exchange results in an improved isomerization catalyst as compared to mordenite in which one or more of the 3 steps of the treatment is omitted.
The process of the present invention involves ammonium exchange of large port mordenite followed by mild acid treatment. Such treatment results in a catalyst more active and selective toward hydrocarbon isomerization than previously known mordenite catalysts. Incorporation of a noble metal into the catalyst further improves its selectively.
The starting material in the following example was large port sodium mordenite, made according to the teaching of U.S. Pat. No. 3,436,174, in pelletized form bonded by a silicious bond. The 1/16" pellets contained 6.1% Na.sub.2 0, and the silica to alumina mole ratio was 10.5 to 1.
The sodium zeolite was treated with 3 to 5 normal NH.sub.4 NO.sub.3 solutions until chemical analysis showed a constant 0.27% by weight of Na.sub.2 O (on an anhydrous basis). The product was washed free of NH.sub.4 NO.sub.3 solution by repeated washings with water. Two hundred grams of the washed product was treated by boiling for four hours in 400 ml. of 0.5 normal HC1. After washing free of acid, the product was found to contain 0.23% Na.sub.2 O, and had a silica to alumina ration of 10.7 to 1, after calcination for 24 hours at a maximum temperature of 550.degree. C.
The testing procedure for isomerization employed a 1 to 1 volume mixture of the mordenite pellets with inert fused alumina aggregate. The process conditions were a temperature of the bed of 480.degree. F., pressure of 450 p.s.i.g., hydrogen to normal pentane feed mole ratio of 7/1 and weight hourly space velocity of 1.00 gram of normal C-5 per gram of catalyst per hour.