Petroleum Analyzer Company, LP

Ingenia Polymers Corporation

Cambridge Viscosity, Inc.

Larry Angelo Spino

Guoxing Yang

David G Anderson

Larry M Youngblood

Scott K Berkhous

Fang Fang

Salvatore D'Uva

Daniel Airey

John Lefas

Viachaslau Urvantsau

David Anthony Malaguti

Sean E Rick

Zach Charlton

Herve Philippe Cleris

George Kalantzakis

George Kalanzakis

An apparatus and method is shown for determining the pumpability limit, freeze point and/or pour point of liquids, particularly fuels, at sub-ambient temperatures. A sample is placed in a viscometer which viscometer is rapidly cooled by a chiller. During cooling, after some measurements of temperature and viscosity, further temperatures and viscosity are approximated using the least squares method, which temperature and viscosity are subsequently measured to determine the pumpability limit. Continuation of the method will also give the freeze point and pour point of the sample being tested.

Viscosity measurement of liquids at subambient temperatures

A thermal oxidation tester is shown for determining thermal stability of a fluid, particularly hydrocarbons when subjected to elevated temperatures. The tendency of the heated fluid to oxidize and (1) form deposits on a surface of a heater tube and (2) form solids therein, are both measured at a given flow rate, temperature and time. The measured results are used to determine whether a fluid sample passes or fails the test. At the beginning of each test, the test sample is aerated with dry air until saturation. Simultaneously, the test equipment is primed to remove pockets of air there from. After each test, the test equipment is flushed to remove the test sample there from.

Auto priming and flushing an apparatus for determining the thermal stability of fluids

A thermal oxidation tester is shown for determining thermal stability of a fluid, particularly hydrocarbons when subjected to elevated temperatures. The tendency of the heated fluid to oxidize and (1) form deposits on a surface of a heater tube and (2) form solids therein, are both measured at a given flow rate, temperature and time. The measured results are used to determine whether a fluid sample passes or fails the test. Sample flow rate is important in the jet fuel thermal oxidation test. Current practice requires manual drop counting or flow confirmation with the use of volumetric glassware. An apparatus is described to precisely measure the flow rate and automatically perform flow rate check using a drip rate method and/or volumetric method.

Drop counter and flow meter for apparatus and method for determining the thermal stability of fluids

A thermal oxidation tester is shown for determining thermal stability of a fluid, particularly hydrocarbons when subjected to elevated temperatures. The tendency of the heated fluid to oxidize and (1) form deposits on a surface of a heater tube and (2) form solids therein, are both measured at a given flow rate, temperature and time. The measured results are used to determine whether a fluid sample passes or fails the test. Results of measurements are recorded in a memory device on one end of the heater tube on which the deposits were made.

Apparatus and method for determining the thermal stability of fluids

A thermal oxidation tester is shown for determining thermal stability of a fluid, particularly hydrocarbons, when subjected to elevated temperatures. The tendency of the heated fluid to oxidize and (1) form deposits on a surface of a heater tube and (2) form solids therein which are both measured at a given flow rate, temperature and time. The measured results are used to determine whether a fluid sample passes or fails the test. Specifically constructed containers used in a thermal oxidation tester are shown. These containers (1) reduce physical contact to hydrocarbon test fuels, (2) reduce exposure to hydrocarbon fuel vapors, (3) reduce environmental impact by reducing chemical spills, and (4) improve overall work flow of test.

Containers used in determining the thermal stability of fuels

A method is described for preparing liquid concentrates of additives for incorporation in polymers, particularly polymers prepared in solution or slurry phase polymerization media. Additive concentrates according to the invention are characterized by a finer dispersion than would result from the direct addition of particulate or granular additives to the same liquid solvent.

Liquid compositions of polymer additives and method for their preparation

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Houston, TX, United States of America

Larry Angelo Spino