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Dive into the research topics where John Ronald Sanderson is active.

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Featured researches published by John Ronald Sanderson.


Catalysis Letters | 1994

OLEFIN OLIGOMERIZATION VIA ZEOLITE CATALYSIS

John Frederick Knifton; John Ronald Sanderson; P. Eugene Dai

Oligomerization of terminal and internal long-chain, linear olefins has been successfully demonstrated using large pore zeolites with high silica-to-alumina ratios as catalysts. Both reactant and product selectivities have been demonstrated using 12-membered ring zeolites for the oligomerization of C12–C18 olefins. The catalytic activity of these zeolites decreases in the order faujasite > mordenite > pentasil; the activity of the Y-zeolites depends primarily upon the silica-to-alumina molar ratio, but not on the total acidity. 1-tetradecene oligomerization, followed by oligomer hydrogenation, yields synthetic lubricant base stocks with excellent physical characteristics.


Applied Catalysis A-general | 1997

Phenol/acetone cogeneration via solid acid catalysis

John Frederick Knifton; John Ronald Sanderson

Abstract Phenol/acetone cogeneration via cumene hydroperoxide (CHP) cleavage has been demonstrated using various classes of novel solid acid catalysts. Mineral acid-treated montmorillonite silica-alumina clays, heteropoly acids impregnated into Group IV oxide supports, fluorophosphoric acid and HF-treated oxides, as well as montmorillonite clays modified with heteropoly acids or certain Lewis acids, are each effective. The influence of solid acid structure upon phenol yields has been examined while minimizing by-product acetophenone, 2-methylstyrene, 2-phenyl-2-propanol, mesityl oxide formation, etc. For the more promising candidates, decomposition of 80% CHP solutions in continuous, plug-flow reactor systems, under mild conditions (ca. 60°C at LHSVs≈10) has been realized.


Catalysis Letters | 2001

Tert-butanol dehydration to isobutylene via reactive distillation

John F. Knifton; John Ronald Sanderson; Melvin E. Stockton

Selective tertiary-butanol (tBA) dehydration to isobutylene has been demonstrated using a pressurized reactive distillation unit under mild conditions, wherein the reactive distillation section includes a bed of solid acid catalyst. Feeding tBA to the middle of the distillation section, anhydrous isobutylene product is recovered as an overhead fraction and co-product water as a bottoms fraction. Suitable solid acid catalysts include zeolite Beta, hydrogen-fluoride-treated β-zeolites, and HF-treated montmorillonite clays. Quantitative tert-butanol conversions have been realized.


Archive | 1996

Use of reactive distillation in the dehydration of tertiary butyl alcohol

John Frederick Knifton; John Ronald Sanderson; Melvin E. Stockton


Archive | 1996

Method for the manufacture of methyl tertiary butyl ether from tertiary butyl alcohol and methanol

Rei-Yu Judy Hwan; Mark Elliott Taylor; John Frederick Knifton; Melvin E. Stockton; John Ronald Sanderson


Archive | 1999

Improved glycol purification

John Ronald Sanderson; Edward T. Marquis


Archive | 1994

Conjoint production of ditertiary butyl peroxide and tertiary butyl alcohol from tertiary butyl hydroperoxide

John Ronald Sanderson; John Frederick Knifton


Archive | 2000

METHODS FOR DECOMPOSING ESTERS AND PURIFYING ALCOHOLS

John Frederick Knifton; John Ronald Sanderson; William Alan Smith; James Douglas Goshinska; Mark Allen Mueller


Archive | 1993

Catalytic decomposition of peroxides to purify a methyl tertiary butyl ether recycle stream

John Ronald Sanderson; John Frederick Knifton


Archive | 2004

Purification of solvents used for the purification of alkylene oxide

John Ronald Sanderson; Mark Allan Mueller; James P. Farone

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