Abstract: In the course of a method for the structural analysis of a chemical compound by data signals measured with the chemical compound being compared with calculated data, a first data signal is generated for at least one first compound having a structure which is similar to the assumed structure and has the same first substructure, but a different substituent Sv (instead of the substituent Sa of the compound being studied) in the substitution position; a second data signal is generated which constitutes the difference between the data from a second Sv-substituted compound and an unsubstituted (third) compound; a third data signal is generated which constitutes the difference between the data from a fourth Sa-substituted compound and an unsubstituted compound; a fourth data signal is generated from the first three data signals, and the measured data signal and the fourth data signal are compared with one another.

Abstract: The selectivity of response of resistive gas sensors to specific gases or vapors is improved by the selection of specified gas-sensitive materials which are not previously known for the applications described, which include detection of hydrocarbons in the presence of CO, H.sub.2 S, SO.sub.2, chlorine, NO.sub.2, CO.sub.2 (especially in low concentrations), CFC's, ammonia, free oxygen by determination of partial pressures, and numerous organic gases and vapors.

Abstract: The present invention relates to measurements of contaminants in the soil and other organic or environmental materials, using a biologically relevant chemical analysis that will measure the amount of contaminants in a given sample that may be expected to be absorbed by a human being ingesting the contaminated soil. According to the present invention, environmental samples to be tested are added to a pre-prepared physiological composition of bile salts and lipids. They are thoroughly mixed and then the resulting mixture is separated e.g. by centrifugation. The supernatant is then analyzed for the presence of contaminants and these concentrations are compared to the level of contaminants in the untreated samples. It is important that the bile salts and lipids be thoroughly pre-mixed to form micelles.

Abstract: The invention provides a gas sensor for selective detection of hydrocarbons in low-oxygen gases, having a capacitive element and a gas-permeable sensitive layer as a dielectric. The sensitive layer is a precious-metal-doped zeolite which has a regular crystalline structure made of primary pores whose diameter is in the order of the gas-kinetic diameter of the gas molecules to be detected.

Abstract: A device for determining at least one petroleum characteristic of a geologic sediment sample placed in a boat, said device including a first heater heating said sample in a non-oxidizing atmosphere, a measuring component determining hydrocarbon-containing products released after feeding the sample into said first heater, a second subsequent heater heating said sample in an oxidizing atmosphere, a measuring component determining the amount of CO.sub.2 contained in effluents discharged from the two heaters, said CO.sub.2 measuring means include a cell for measuring continuously CO.sub.2 throughout heating of the first and second heaters and a measuring component determining the amount of CO contained in the effluents discharged from the two heaters, and thereby allowing determination of said petroleum characteristic.

Abstract: A method of determining or predicting a value P.sub.x of a property of a feed X to a steam cracking process or yield of said process, which method comprises measuring the absorption D.sub.ix of said material at more than one wavelength in the region 600-2600 nm, comparing signals indicative of said adsorptions or a mathematical function thereof with signals indicative of absorptions D.sub.im or mathematical function thereof at the same wavelength for a number of standards S in a bank for which the said property or yield P is known, and choosing from the bank at least one standard S.sub.m with property P.sub.m said standard having the smallest average value of the absolute difference at each wavelength i between the signal for the material and the signal for the standard S.sub.m to obtain P.sub.x, with averaging of said properties or yields P.sub.m when more than one standard S.sub.m is chosen. If desired the method can be used as such to control the steam cracking process by comparison of P.sub.

Abstract: A method for the quantitative determination of dissolved oxygen in a liquid fuel includes the steps of doping a sample of the fuel with a preselected concentration of a probe material including a luminophor which exhibits luminescence of wavelength which is quenched by oxygen dissolved in the fuel, illuminating the fuel with light from a coherent light source, such as a laser, of a wavelength which induces the luminescence in the luminophor, and thereafter measuring the change with time of the luminescence from the luminophor in the fuel and determing from the change with time of the luminescence the concentration of oxygen in the fuel.

Abstract: An electrochemical cell is coupled on-line with a mass spectrometer to achieve minimal response time in a system called rapid electrochemical-mass spectrometry (EC/MS). Many large, nonpolar compounds that could not be analyzed by prior ES/MS techniques may now be analyzed. Ionic and polar intermediates and products generated by electrochemical reactions may be probed with very short response times prior to their analysis. Ions are generated by electrochemical oxidation or reduction immediately prior to electrospray release, pneumatic nebulization, or outlet heating. The on-line coupling of an electrochemical cell to electrospray mass spectrometry permits the fast identification of ionic intermediates (both radicals and non-radicals), as well as products generated from electrochemical reactions and from ensuing solution-phase reactions. Neutral compounds that are otherwise difficult to analyze by ordinary electrospray mass spectrometry may now be analyzed. Preferred three-electrode cells are disclosed.

Abstract: An apparatus for on-line measuring physical property data of hydrocarbon products such as octane number, cetane number, density, vapour pressure and the like or gasoline/alcohol ratio, comprising means for providing (N)IR radiation in a predetermined spectral range; means for transmitting light at selected wavelengths in the (N)IR spectral region; means for delivering light from said transmitting means to a hydrocarbon product line; means for allowing an optical path length in the hydrocarbon product line; means for detecting the light transmitted through the said optical path; means for providing the obtained signal to be input to processing equipment for spectral analysis and correlating the spectral data to the physical property data of hydrocarbon products such as octane number, cetane number, density, vapour pressure and the like or gasoline/alcohol ratio.

Abstract: A method allowing fast assessment of at least one petroleum characteristic of geologic sediments from a sample of these sediments, said method comprising heating the sample in a non-oxidizing atmosphere, and which method comprises different temperature rise stages; determining at least three magnitudes S.sub.1r, S.sub.2a and S.sub.b representative of the quantity of hydrocarbons contained in said sample, and deducing at least one petroleum characteristic of the geologic sediment from these three magnitudes.

Abstract: The present invention is a method to determine the chemical concentration of one or more of a number of the constituent classes of a feed to a catalytic cracking process. These constituent classes which are referred to as "lumps", include 14 different molecular types in 4 different boiling range fractions. A specific lump will include all individual molecular components which are expected to react in a similar way in the catalytic cracking unit.

Abstract: The present invention relates to a method for determining at least one petroleum characteristic of a geologic sediment sample heated in a non-oxidizing atmosphere and an oxidizing atmosphere. The sample is heated to a first temperature value below 200.degree. C. for a predetermined period of time and then to a second temperature value ranging between 600 and 850.degree. C. according to a temperature gradient between 0.2.degree. C. and 50.degree. C./min. Carbon dioxide and carbon monoxide are continuously measured during the temperature stages in order to determine at least one petroleum characteristic, wherein said petroleum characteristic comprises a quantity of organic oxygen, inorganic oxygen, total organic carbon, or inorganic carbon.

Abstract: A method of evaluating at least on type of pollution characteristic in a soil sample contaminated by hydrocarbon compounds, a method wherein the soil sample is first heated in a non-oxidizing atmosphere, then in an oxidizing atmosphere. The method comprises several temperature rise stages from which at least five quantities Q.sub.0, Q.sub.1, Q.sub.2, Q.sub.3 and Q.sub.4 are measured, wherein the quantities represent concentrations of hydrocarbon compounds in the soil sample. At least one type of pollution characteristic of the sample is determined from quantities Q.sub.0, Q.sub.1, Q.sub.2, Q.sub.3 and Q.sub.4.

Abstract: The present invention relates to a process for indicating the presence of organic vapors comprising the steps of determining the color, absorption or emission spectra of a Pt--Pt double-complex salt of platinum or a neutral platinum complex in the absence of organic vapor, exposing said double-complex salt of platinum or a neutral platinum complex to a gaseous environment, determining the color, absorption or emission spectra of said double-complex salt of platinum or a neutral platinum complex after exposure to said gaseous environment, and comparing the color, absorption and/or emission spectra of said double-complex salt of platinum or a neutral platinum complex in the absence of organic vapor with the color, absorption and/or emission spectra of said double-complex salt of platinum or a neutral platinum complex after exposure to said gaseous environment to determine if there is a difference in the color, absorption and/or emission spectra.

Abstract: A method for enhancing detection sensitivity of suspected trace amounts of organic analytes and particularly semivolatile organic analytes extractable from a sample by an organic solvent carrier matrix and subsequent extraction and analysis of said trace organic analytes by SPME wherein the improvement comprises exchanging the organic solvent carrier matrix containing the trace organic analytes for an aqueous carrier matrix before performing SPME fiber extraction and detection of the trace organic analytes.

Abstract: A process for measuring and controlling the concentration of a solution at an aim point of an amide solvent and aramid polymers having aromatic and aliphatic carbon-hydrogen bonds that overlap using a near-infrared analyzer.

Abstract: A method for determining the amount of photoreactive polynuclear aromatic compound in a sample is described. A sample containing an unknown amount of a photoreactive polynuclear aromatic compound is mixed with a known quantity of a polyhalogenated organic compound and exposed to light of a known wavelength for a known length of time. The quantity of the photoreaction product which results from the light exposure is measured by absorption spectroscopy. Comparison of the absorption measurement to a standard curve allows determination of the concentration of the photoreactive aromatic compound. The simplicity of the method makes it suitable for on-site testing. The method can be used to test for photoreactive compounds in various media, such as soil, aqueous samples, and oil.

Abstract: Halo, azido, and amino cyclodextrin/epichlorohydrin copolymers, methods of preparing the copolymers, and the use of the copolymers for removing aflatoxins and phytoestrogens from a sample, for detecting the presence of aflatoxins and phytoestrogens, and for quantifying aflatoxin and phytoestrogen levels.

Abstract: A process of continuously controlling at least one characteristic of a simulated moving bed para-xylene separation process has been developed. The characteristics controlled may be the purity or the recovery of the para-xylene. The process involves measuring the concentrations of the para-xylene, meta-xylene, ortho-xylene, and ethylbenzene in the pumparound or pusharound stream, calculating the value of the characteristic, and making required adjustments to operating variables according to an algorithm which relates changes in the value of the characteristic to the changes in the concentrations of the components resulting from changes in the operating variables. The process is unique in that the necessary quantity of data to control the separation is rapidly generated, thereby providing increased efficiency, precision, and accuracy.

Abstract: A method and test kit for the detection of hydroxy substituted aromatic compounds using a titanium film (12, 23) which reacts with the compound to change the light absorbance. Preferred films are prepared by reaction of a titanium alkoxide with an aliphatic carboxylic acid. The change in light absorbance of the film is preferably detected with an ultraviolet-visible spectrophotometer. Preferably the film is provided on a transparent slide (22) or on an inside wall of a spectrophotometer cell (10). The cells (10 and 20) are provided with covers (13 and 14) for holding the solution to allow the hydroxy substituted compounds to react with the film.

Abstract: The invention provides a method and an apparatus for measuring asphaltene precipitation in a petroleum product. The inventive method quantifies the precipitation by measuring changes in the petroleum product's conductivity or capacitance. The inventive apparatus comprises a measuring cell adapted to be filled with a petroleum product or a solution of the product and a flocculant, together with an instrument electrically coupled to the measuring cell for measuring the product's or solution's conductivity or capacitance.

Abstract: The invention pertains to an immunoassay method for determining the presence of volatile organic compounds in aqueous, soil and air samples by simultaneously collecting and testing a sample volume suspected to contain such organic compounds. As a major problem in the assay of such materials is their rapid evaporation, the present immunoassay is specifically designed to eliminate or minimize the evaporation of the volatile organic analyte during sample handling as well as during the assay process itself. The immunoassay method is based on an assay vessel which has a lower portion, in which the immunoassay actually takes place, and an inert upper portion, which can hold a sufficiently large volume of sample to prevent or minimize evaporation of the organic compound from the smaller volume in the lower portion.

Abstract: The present invention provides methods, reagents and kits for determining the presence of aromatic ring-containing compounds by immunoassay techniques, including enzyme, fluorescent, chemiluminescent and biosensor immunoassay, as well as radioimmunoassay. Monoclonal and polyclonal antibodies may be used in the practice of the present invention.

Abstract: A method for detecting low level of alkylbenzene or mineral oil impurity in polyol ester lubricants for compressors. This method comprises mixing a mixture of alcohol and water with a sample of the lubricant and then observe the presence or absence of turbidity.

Abstract: A method for the identification of whether a lubricant in a compressor is an alkylbenzene or a naphthenic oil. This method comprises adding 3,3-bis (p-hydroxyphenyl) phthalide and observing whether there is an absence or presence of turbidity.

Abstract: Antibodies are raised against immunogens which include an aromatic ring moiety, preferably the compound 6-aminohexyl-p-tolylacetamide, which immunologically cross-react with small aliphatic organic compounds. These antibodies are useful in immunoassay methods for detecting a class of very small organic molecules such as 1,1-dihaloethylene and 1,1,2-trihaloethylene, whether alone or as a functional group on another molecule. Such antibodies and methods provide important tools for detecting significant environmental pollutants.

Abstract: A fiber-optic sensor or analytical apparatus and associated method which utilizes the combination of (a) a solid, semi-solid or liquid sensor body which is capable of selectively dissolving the analyte compound to be detected and analyzed into the sensor body from the mixture or environment in which the compound is present and excluding undesired or interfering components, (b) a radiation source for directly radiating the analyte compound molecules to excite same to an elevated energy state, thereby causing the analyte compound itself to luminesce while dissolved in the sensor body, and (c) a radiation detector for detecting and measuring the light emitted from the excited analyte compound molecules when they return to a lower energy state. The selective dissolving sensor body provides a controlled environment in which both the source light directly excites the analyte molecules and the excited molecules emit light which is detected and measured.

Abstract: Detecting the presence of PAC's in the effluent of a combustions system by detecting the presence of a high molecular weight PAC's having five or more rings. A position along the effluent stream is selected at which high molecular weight PAC's may be present. The effluent is illuminated with radiation having a wavelength absorbed by the high molecular weight PAC's in the gas phase. The fluorescence from the illuminated effluent is detected, and analyzed by comparison to the known fluorescence of high molecular weight PAC's in the gas phase to determine the presence of the PAC's in the effluent. The effluent composition may be controlled in response to the detection.

Abstract: A quantitative method including separating a mixture of olefins, aromatics, and saturates by supercritical fluid chromatography to obtain an eluent stream that over a first time period contains a mixture of olefins and saturates, and over a second time period contains aromatics, and passing the eluent first to an ultraviolet absorption detector (UV). Importantly, the eluent is irradiated in the UV detector at a wavelength capable of producing an ultraviolet absorbance response of olefins that is independent of specific olefins present, and preferably is substantially similar to a mass detector response for olefins. From a combination of UV and mass response, the mass of the olefins in the mixture of olefins and saturates can be determined. Thereafter, the eluent is passed to a mass detector whereby the mass of the mixture of saturates and olefins is determined and then the mass of the aromatics is determined.

Abstract: A process to find the stability of mixtures of oils, including that of shale oils, and of distilled fractions of petroleum oils is described, which process may be extended to any mixtures of non-ionic compounds containing a non-polar hydrocarbon moiety and a heteroatomic polar moiety, and such polar and non-polar moieties may lie in the same or different molecules.

Abstract: The present invention provides fluorescence-based methods for sensitively detecting total ADH activity in human sera and selectively measuring the activity of different classes of ADH in human sera and other body fluids and tissues. The present invention also provides highly purified Class I, Class II, and Class III isozymes, and methods for their purifiation. The class of substrates consisting of various naphthaldehydes and quinoline aldehydes provide the requisite sensitivity and selectivity for measurements of the activity of ADH and individual ADH classes. These fluorescence-based methods may serve as a diagnostic aid in disease assessment, in particular, diagnosis of alcohol abuse, alcoholism, alcohol consumption, altered alcohol sensitivity or tolerance.

Abstract: The methods and test kit of the present invention provide a fast, inexpensive, reproducible, simple, and accurate method for optimizing the dosage of an asphaltene dispersant antifouling agent for a given crude oil containing asphaltenes. A method is provided wherein a sample of the crude oil is diluted with a quantity of an aromatic organic solvent. To the diluted crude oil is added a known amount of the antifouling agent being evaluated. A portion of the diluted crude oil containing the antifouling agent is removed and mixed with a quantity of a liquid paraffinic hydrocarbon. The concentration of materials which remain dispersed in the liquid paraffinic hydrocarbon is measured. The inventive methods are useful to evaluate a single dose of an antifouling agent or may be used to simultaneously evaluate a plurality of doses in order to determine which dose is most effective for a given sample of crude oil.

Abstract: Mid-distillate hydrocarbon fuels, preferably having initial boiling points above 350.degree. F., are separated e.g. by prep-HPLC into non-aromatic and aromatic fractions which are used to set 0% aromatics (the non-aromatics) and 100% aromatics (the aromatics) on an NIR spectrophotometer. From NIR aromatic band absorbances of unknown samples, their percent aromatics is determined using this two-point calibration and the Beer-Lambert equation. Preferred NIR bands of 1650-1700 and 2120-2256 exhibit excellent correlation with aromatics content.

Abstract: The diamondoid compound content of a hydrocarbon gas sample stream is measured in a process and apparatus for the controlled precipitation and collection of diamondoid compounds.

Abstract: Single or multi-cell reservoir sensors with single illumination sources and one or more detectors per cell unit have an arrangement whereby a gaseous, vapor or liquid sample enters the cell body and interacts with a sensing solution to detect and quantify a given species. Entrance of the sample into the sensor is through an opening in the cell body which may be covered with a membrane to contain the sensing reagent and to presort the species entering the cell. Reservoir cells can be used with organic, inorganic or biochemical sensing materials. A variety of sensors as alcohol, drugs of abuse, organic halides, cyanide and inorganic ions are provided.

Abstract: A hydrocarbon gas detection system utilizes a heat chamber or oven to maintain the system at a temperature that will support cracking of hydrocarbon gases. A gas chamber which is located inside the oven is used to contain the flow of gases under analysis and to pass these gases over a first temperature sensing device. A catalyzing material is associated with the first temperature sensing device, either by placing it very near the temperature sensing device or by coating the temperature sensing device with the catalyzing material. A second temperature sensing device is located inside the heat chamber or oven, either outside the gas chamber, or inside the gas chamber, but separated from the first temperature sensing device. The output of the first and second temperature sensing devices extend outside of the furnace to measurement and/or display instrumentation. With this system, the gas sample under analysis is passed through the gas chamber and brought into contact with the first temperature sensing device.

Abstract: A method is provided for testing the activity of a catalyst for a chemical reaction in which naphthalene is reversibly hydrogenated by gaseous hydrogen into tetralin, which avoids the need to pressurize a test vessel with hydrogen, enables simple apparatus to be used and gives good accuracy. Tetralin and catalyst are introduced into a sealed container, the container is heated to a reaction temperature for a predetermined time, and the amount of naphthalene formed by dehydrogenation is determined. The method is applicable to the measurement of catalyst activity for catalysts used in the production by hydrogenation of coal-derived liquids.

Abstract: Methods and apparatus for analyzing a hydrocarbon sample are provided. The apparatus employs a highly polar column to separate the aromatics from non-aromatic components. The non-aromatic effluent from the highly polar column is passed to a 13X MSCOT column and a first less polar column. In a second configuration the highly polar column is backflushed into a second less polar column. The 13X MSCOT column separates isoparaffins, normal paraffins, and naphthenes by carbon number while the first less polar column individually separates the paraffins and naphthenes. The second less polar column is employed to separate individual aromatics.The method for analyzing a hydrocarbon sample separates the aromatics of the sample from the isoparaffins, normal paraffins, and naphthenes. The isoparaffins, normal paraffins, and naphthenes are then separated and detected by carbon number. Simultaneously, the individual non-aromatic components are separated and detected.

Abstract: A method for measuring the halogenated organic compound content, e.g., polychlorinated biphenyl ("PCB") content, of soil samples may effectively be carried out with an inexpensive, disposable (that is, single-use) field test kit. The method includes contacting a weighted soil sample suspected of containing PCB or some other organohalogen contaminant with a pre-mixture of water and an organic solvent in which water is slightly soluble. The water extracts any inorganic halides which may be present and would adversely affect the accuracy of the test. The organic solvent wets the moist soil sample sufficiently to extract any PCB therein. The resultant organic solvent phase is separated from the soil sample and aqueous phase, dried by passage through a moisture-adsorbent material to remove or at least greatly reduce its moisture content, and analyzed by means of a color-change titration to determine halide content, and thereby the PCB (or other organohalogen) content, of the soil sample.

Abstract: An apparatus, which may be embodied in a disposable field test kit, and a test method serves to measure the halogen (bromine, chlorine, iodine) content, especially the chlorine content, of hydrocarbon liquids. The apparatus includes a sampling device in which a quantity of the hydrocarbon liquid, such as a used oil, is suctioned into a frangible collector such as a capillary tube to control sample size, and the tube is deposited into a flexible container which also contains frangible ampules holding pre-measured quantities of reagents, including a solvent for the sample. The container is squeezed to break the tube and ampules to release their contents in prescribed order. The sample is first solvated, then reacted with an alkali metal reagent which will form halides from halogen material present, extracted into an aqueous phase, titrated, and contacted with a color change indicator which acquires a characteristic color dependent upon the halogen material content.

Abstract: A simple, on-site, field test method and kit for aromatic contamination in a water sample is provided. In the field test, the water sample is first extracted using an alkyl halide extractant, with a Friedel-Crafts Lewis acid catalyst being added to the resulting extractant phase. A reaction product is thereby produced having a characteristic color indicative of the amount and type of aromatic contamination.

Abstract: A sample of a hydrocarbon oil containing asphaltenes is chromatographically analyzed by forming a mixture of the oil with a weak solvent. The mixture is passed in contact with a column of a stationary phase of fine solid particles of fully functionalized material, followed by a weak solvent. The solvent, after recovery from the column, is analyzed for aromatics by UV-absorption of UV radiation in the range 200 to 400 nm. The absorbance of the UV light by the irradiated eluents across the UV wavelength range is monitored and the integral of absorbance is derived as a function of photon energy across the wavelength range. The magnitude of the derived integral in at least one time interval corresponding with aromatics in the eluent from the stationary phase is measured as an indication of the level of aromatics in the oil sample. The weak solvent may be followed by a strong solvent which, in turn, may be followed by a strong solvent which is modified by the addition of a hydrogen bonding solvent.

Abstract: A sensitive method for the determination of water in the presence of common interferences is presented. The detection system is based on the effect of water on the equilibrium which results from the reaction aryl aldehydes, such as cinnamaldehyde and methanol in the eluent to form cinnamaldehyde dimethylacetal, plus water. This equilibrium is shifted in a catalytic atmosphere of a hydrogen ion form past column reactor. The extent of the shift and the resulting change in absorbance are proportional to the amount of water present.

Abstract: The present invention provides a general assay methodology suitable for the detection of organic analytes which are neither aldehydes nor ketones and for inorganic substances. The methodology utilizes prepared sensitized films of derivatizing agents and specific developer solutions for the selective and controlled formation of light scattering crystals whose presence serves as a qualitative and/or quantitative measure of the individual analyte of interest in the sample.

Abstract: A method for analyzing marker dye present in the parts per million range in gasoline is provided using a solid-phase extraction technique with formation of the colored complex in the extraction column as well as a method for detecting the adulteration of gasoline containing the marker.

Abstract: A chromatographic method for the determination of individual phenols in water by adding a halogenating agent to the water, e.g., using the bromate-bromide reaction to generate tribromide ions which react with the phenols to form bromo-derivatives of the phenols, then to permeate the bromo-derivatives across a membrane, e.g., a silicone rubber membrane, into a liquid extractant, e.g., a dilute aqueous solution of sodium hydroxide and acetonitrile, and then determining the permeated bromo-derivatives in the liquid extractant by chromatography, e.g., by injecting the liquid extractant containing the permeated bromo-derivatives into a reverse phase liquid chromatographic system.

Abstract: A method and/or system for rapidly determining the average composition and characteristics of a hydrocarbon mixture comprising thermally cracking the mixture to form a gaseous product, measuring the ratios or proportions of the individual components in the gaseous product, and comparing the ratios of the components present in the gaseous products with a known property of the hydrocarbon feed mixture and obtaining the average composition and intrinsic properties of the hydrocarbon feed.

Abstract: A very rapid, sensitive method if provided for determination of the potential mutagenicity and/or carcinogenicity of certain petroleum oils by nitration of the oil and comparison of the light absorbance of its nitrated material with that obtained from one or more oils of known mutagenicity and/or carcinogenicity.

Abstract: A process for determining the polarity of a crude oil or heavy fraction thereof in which the retention times are measured when a series of substances is contacted with a chromatographic column of crude oil, the retention times are measured when these substances are contacted with a chromatographic column of a second substance usually non-polar and the relative polarity of the oil determined from the times measured.

Abstract: A sample of a hdyrocarbon oil containing asphaltenes is chromatographically analyzed by forming a mixture of the oil with a weak solvent. The mixture is passed in contact with a column of a stationary phase of find solid particles of fully functionalized material, followed by a weak solvent. The solvent, after recovery from the column, is analyzed for aromatics by UV-absorption of UV radiation in the range 200 to 400 nm. The absorbance of the UV light by the irradiated eluents across the UV wavelength range is monitored and the integral of absorbance is derived as a function of photon energy across the wavelength range. The magnitude of the derived integral in at least one time interval corresponding with at least aromatics in the eluent from the stationary phase is measured as an indication of the level of aromatics in the oil sample. The weak solvent may be followed by a strong solvent which, in turn, may be followed by a strong solvent which is modified by the addition of a hydrogen bonding solvent.