Thomas F Brady

US Patent:

43191282, Mar 9, 1982

Filed:

Feb 5, 1980

Appl. No.:

6/118772

Inventors:

John Dow - Rumson NJ
William A. Oetting - Green Brook NJ
Richard J. Yessian - Martinsville NJ
Thomas J. Brady - Linden NJ

Assignee:

Lockheed Electronics Co., Inc. - Plainfield NJ

International Classification:

B67D 524
G06C 2900
G06F 1556

US Classification:

235 61PD

Abstract:

Microprocessor controlled flow metering apparatus employs mechanically coupled registers driven by a positive displacement or other flow meter to display fluid volume dispensed during a monitored transaction--and as a cumulative total over time. User adjustable electrical switch decades electrically enter computational scale factor variables such as price per gallon and tax rate. The stored program controlled microprocessor computes all desired output variables (fuel cost, tax)--and outputs the variables in predesignated fields onto a printed ticket (invoice) while controlling printer carriage movement and solenoid actuation. In accordance with varying aspects of the invention, mechanical and software security is provided to ensure proper correlation between customer fluid (e. g. , fuel) receipt and billing.

US Patent:

39473740, Mar 30, 1976

Filed:

Jul 16, 1974

Appl. No.:

5/489015

Inventors:

Frank Fred Loffelman - Somerville NJ
Thomas Eugene Brady - Piscataway NJ

Assignee:

American Cyanamid Company - Stamford CT

International Classification:

C11D 754

US Classification:

252102

Abstract:

Halotriazines of the formula: ##SPC1## Where X represents halogen; and R. sub. 1 and R. sub. 2 individually represent halogen, hydroxy, mercapto, alkyl, alkenyl, alkoxy, alkylmercapto, aryl, aryloxy, arylmercapto, di-alkoxyphosphinyl or ##EQU1## where R. sub. 3 and R. sub. 4 individually represent hydrogen, alkyl, alkoxy, cyanoalkyl, hydroxyalkyl, carboxyalkyl, chloroalkyl, alkoxyalkyl, acyloxyalkyl, sulfonalkyl, aryl, haloaryl, sulfoaryl, acylaminoaryl, carbamoylalkyl or arylsulfonyloxyalkyl, or where R. sub. 3 and R. sub. 4 taken together complete a ring structure selected from morpholine, piperazine, piperdine, succinimide, malemide and phthalimide rings; are bleach activators of high activating strength and good storage stability in peroxygen bleaching compositions.