American Cyanamid Company

Mark Allan Higgins

Arthur Maurice Schiller

Charles Richard Witschonke

Dae Suk Song

Richard Joseph Duffy

John A Sedlak

Amy P Essenfeld

An improved process for the synthesis of esters of 3,5,6-trichlorosalicylic acid in quantitative yield comprises reacting the acid with an alcohol under distillation conditions in the presence of a titanium ester or chelate catalyst, whereby byproduct ether formation from the alcohol is suppressed. The process is especially applicable to a process by which salicylic acid is chlorinated first in concentrated sulfuric acid and then with iodine catalyst to make the trichlorosalicylic acid which is extracted and then reacted with an alcohol and a titanium catalyst to make the ester.

Process for preparing esters of 3,5,6-trichlorosalicyclic acid

A process for inhibiting scale formation using a low molecular weight hydrolyzed polyacrylamide prepared by a process involving simultaneously and continuously charging separate streams of acrylamide monomer, ammonium persulfate (as catalyst) and mercaptoalkanoic acid (as chain transfer agent) to a reaction zone containing water under reflux, the rate of charging being such that the heat of polymerization is sufficient to maintain reflux in the reaction zone without exceeding the capacity of the condenser to remove the heat of reaction, and then reacting the polymer product with sufficient aqueous caustic to hydrolyze from about 60 to 90% of the amide groups in the polymer product.

Low molecular weight hydrolyzed polyacrylamide used as a scale inhibitor

A low molecular weight hydrolyzed polyacrylamide having exceptional effectiveness as a scale-inhibiting agent is prepared by a process involving simultaneously and continuously charging separate streams of acrylamide monomer, ammonium persulfate (as catalyst) and mercaptoalkanoic acid (as chain transfer agent) to a reaction zone containing water under reflux, the rate of charging being such that the heat of polymerization is sufficient to maintain reflux in the reaction zone without exceeding the capacity of the condenser to remove the heat of reaction, and then reacting the polymer product with sufficient aqueous caustic to hydrolyze from about 60 to 90% of the amide groups in the polymer product.

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Gullford, CT, United States of America

Mark Allan Higgins