Abstract: Various embodiments of the present disclosure pertain to nanocomposites for detecting hydrocarbons in a geological structure. In some embodiments, the nanocomposites include: a core particle; a polymer associated with the core particle; a sulfur-based moiety associated with the polymer; and a releasable probe molecule associated with the core particle, where the releasable probe molecule is releasable from the core particle upon exposure to hydrocarbons. Additional embodiments of the present disclosure pertain to methods of detecting hydrocarbons in a geological structure by utilizing the nanocomposites of the present disclosure.

Abstract: Various embodiments of the present disclosure pertain to nanocomposites for detecting hydrocarbons in a geological structure. In some embodiments, the nanocomposites include: a core particle; a polymer associated with the core particle; a sulfur-based moiety associated with the polymer; and a releasable probe molecule associated with the core particle, where the releasable probe molecule is releasable from the core particle upon exposure to hydrocarbons. Additional embodiments of the present disclosure pertain to methods of detecting hydrocarbons in a geological structure by utilizing the nanocomposites of the present disclosure.

Abstract: An apparatus and process for simulation of field fluid flow conditions under elevated temperature and pressure conditions of oil and gas production, refining, cooling towers, desalinization. The process involves evaluating inhibitor action in reduction of a specified chemical reaction under simulated field aqueous flow conditions by forming first and second aqueous flow streams having a preset concentration of anions and cations, respectively, for the specified chemical reaction with at least one of these streams having a concentration of the inhibitor to inhibit the specified chemical reaction. These streams are combined to form a single process stream where the specified chemical reaction may take place. The process is repeated with successive reductions in inhibitor until detecting the specified chemical reaction in the process stream.

Abstract: A process for measurement of low levels of phosphonates in brine waters wherein the phosphonate samples are acidified with hydrochloric acid promptly upon removal from an oil or gas well to prevent phosphonate precipitation or adsorption. The hydrochloric acid acidified phosphonate is digested in the presence of an oxidizing agent at elevated temperature and pressure for sufficient time to oxidize substantially all of the phosphonate to orthophosphate. The phosphorous containing compound is extracted with an organic extractant, preferably selected from the group consisting of methyl iso-butyl ketone/cyclohexane mixture and ethyl acetate, followed by color development for absorption spectrophotometry.