Determination of polycyclic aromatic hydrocarbons in water using nanoporous material prepared from waste avian egg shell
US-2015377752-A1 · Dec 31, 2015 · US
US10241100B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10241100-B2 |
| Application number | US-201414228152-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 27, 2014 |
| Priority date | Mar 27, 2014 |
| Publication date | Mar 26, 2019 |
| Grant date | Mar 26, 2019 |
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A method for determining a first concentration of a first component in an aqueous solution, the surface tension of which is altered by the presence of the first component. The method can include identifying a second concentration of at least one second component in the aqueous solution. The at least one second component can also alter the surface tension of the aqueous solution. The method can further include comparing a plurality of dynamic surface tension measurements of each of a plurality of aqueous test solutions with at least one dynamic surface tension measurement of the aqueous solution to determine the first concentration. The plurality of aqueous test solutions can include the first component at a plurality of concentrations and the at least one second component at the second concentration.
Opening claim text (preview).
What is claimed is: 1. A method comprising: obtaining a first aqueous sample from a well; identifying a background component that alters a surface tension of the first aqueous sample; measuring a concentration of the background component of the first aqueous sample; creating a synthetic aqueous solution comprising the background component at the measured concentration; conducting a plurality of dynamic surface tension measurements with the synthetic aqueous solution comprising a target component at a plurality of pre-determined concentrations; obtaining calibrative dynamic surface tension curves of the synthetic aqueous solution as a function of the concentration of the target component based on the plurality of dynamic surface tension measurements; obtaining a second aqueous sample from the well; determining the concentration of the target component in the second aqueous sample based on the calibrative dynamic surface tension curves. 2. The method according to claim 1 , wherein the background component is selected from the group consisting of an inorganic material, a friction reducer, a scale inhibitor, a biocide, an emulsion breaker, a pour point depressant, a water clarifier, a shale and clay stabilizer, an antifoam, an H2S and O2 scavenger, a corrosion inhibitor, and combinations thereof. 3. The method according to claim 1 , wherein the target component is a surfactant. 4. The method according to claim 1 , wherein the target component is one selected from the group consisting of nonionic surfactants, ionic surfactants, am photeric surfactants, and combinations thereof. 5. The method according to claim 4 , wherein the nonionic surfactant is selected from the group consisting of an ethylene glycol monostearate, a propylene glycol myristate, a glyceryl monostearate, a glyceryl stearate, a polyglyceryl-4-oleate, a sorbitan acylate, a sucrose acylate, a polyethylene glycol (PEG-150) laurate, a polyethylene glycol (PEG-400) monolaurate, a polyoxyethylene monolaurate, a polysorbate, a polyoxyethylene octylphenylether, a polyethylene glycol (PEG-1000) cetyl ether, a polyoxyethylene tridecyl ether, a polypropylene glycol butyl ether, a stearoyl monoisopropanolamide, a polyoxyethylene, a hydrogenated tallow amide, a fatty acid glycerine ester, a sorbitan fatty acid ester, a sucrose fatty acid ester, a polyglycerine fatty acid ester, an alcohol ethylene oxide adduct, a polyoxyethylene alkyl ether, a polyoxyethylene alkyl allyl ether, a polyoxyethylene lanolin alcohol, a polyoxyethylene fatty acid ester, a polyoxyethylene glycerine fatty acid ester, a polyoxyethylene propylene glycol fatty acid ester, a polyoxyethylene sorbitol fatty acid ester, a polyoxyethylene castor oil, a castor oil derivative, a polyoxyethylene lanolin derivative, a polyoxyethylene fatty acid amide, a polyoxyethylene alkyl amine, an alkylpyrrolidone, a glucamide, an alkylpolyglucoside, a monoalkanol amide, a dialkanol amide, a polyoxyethylene alcohol monoamide, a polyoxyethylene alcohol diamide, a alkylamine, and combinations thereof. 6. The method according to claim 1 , wherein the target component is an ionic surfactant. 7. The method according to claim 6 , wherein the ionic surfactant is an anionic surfactant selected from the group consisting of fatty acid soaps, ether carboxylic acids and salts thereof, alkane sulfonate salts, a-olefin sulfonate salts, sulfonate salts of fatty acid esters, alcohol sulfate ester salts, fatty alcohol ether sulfate salts, alcohol phosphate ester salts, fatty alcohol ether phosphate ester salts, condensates of fatty acids and amino acids, collagen hydrolysate derivatives and combinations thereof. 8. The method of claim 1 , wherein determining the concentration of the background component in the second aqueous sample comprises comparing the dynamic surface tension of the second aqueous sample to the calibrative dynamic surface tension curves. 9. The method of claim 1 , wherein determining the concentration based on the calibration curve comprises plotting a linear portion of a slope of each of the dynamic surface tension curves versus concentration of the target component. 10. The method of claim 1 , wherein the aqueous test solution is a synthetic brine matching the ionic concentration of water from the oil well. 11. The method of claim 1 , adjusting the concentration of the target component in the second aqueous sample.
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