Abstract: The present invention is a method to identify a refinery solid foulant of unknown composition including the following steps: obtaining a solid foulant sample, removing trapped feed from the sample with a solvent to obtain an insoluble sample, scanning the insoluble sample with a scanning electron microscope and energy dispersive x-rays, performing a thermal gravimetric analysis including an ash test on the insoluble sample to determine the presence of polymer, coke and inorganic elements, performing an elemental analysis on the insoluble sample for the elements carbon, hydrogen, sulfur, nitrogen, halogens, and metals, performing an optical microscopy on the insoluble sample to determine the presence of wax, asphaltenes, anisotropic coke and isotropic coke, and identifying the solid foulant.

Abstract: Systems and methods for minimizing extraneous forces and calculating corrected weights of samples based on buoyancy factors for a thermogravimetric analyzer (TGA). The TGA includes a balance chamber and a furnace configured to heat a sample. A null balance is provided in the balance chamber and is used to measure the sample weight change during heating. The furnace includes a cylinder open at the top to receive a sample. The bottom of the cylinder is closed except for a small hole that allows a thermocouple to pass through. An infrared heat source may be provided to heat the cylinder. The balance chamber can be thermally isolated from the furnace using an actively cooled plate and a system of heat shields disposed between the furnace and balance chamber. A thermocouple disk is further provided to limit gas flow in the furnace and increase reliability of sample weight measurements.

Abstract: Systems and methods for minimizing extraneous forces and calculating corrected weights of samples based on buoyancy factors for a thermogravimetric analyzer (TGA). The TGA includes a balance chamber and a furnace configured to heat a sample. A null balance is provided in the balance chamber and is used to measure the sample weight change during heating. The furnace includes a cylinder open at the top to receive a sample. The bottom of the cylinder is closed except for a small hole that allows a thermocouple to pass through. An infrared heat source may be provided to heat the cylinder. The balance chamber can be thermally isolated from the furnace using an actively cooled plate and a system of heat shields disposed between the furnace and balance chamber. A thermocouple disk is further provided to limit gas flow in the furnace and increase reliability of sample weight measurements.

Abstract: A biosensor apparatus for detecting a binding event between a ligand and receptor. The apparatus includes a biosensor surface and surface-bound two-subunit heterodimer complexes composed of first and second, preferably oppositely charged peptides that together form an .alpha.-helical coiled-coil heterodimer. The first peptide is attached to the biosensor surface, and the second peptide carries the ligand, accessible for binding by a ligand-binding agent. Binding of anti-ligand binding agent to the surface-bound ligand is detected by a suitable detector. A ligand-specific biosensor surface can be readily prepared from a universal template containing the first charged peptide, by addition of a selected ligand attached to the second peptide.

Abstract: A method for determining the susceptibility of a sample of Zircaloy alloy to nodular corrosion. A specimen of such Zircaloy sample is annealed at a temperature within a temperature range bounded at its upper limit by the temperature T.sub.c being the temperature at equilibrium wherein sufficient solute would exist in the (.alpha.-matrix of the particular zircaloy to resist nodular corrosion, and bounded by a lower temperature, such temperature being the temperature of the (.alpha.+precipitate)/(.alpha.+.beta.+precipitate) transus for the particular Zircaloy sample. For Zircaloy-2, such temperature range is from approximately 825.degree. C. to 841.degree. C. The specimen is maintained at such selected temperature within such temperature range for a measured period, and subsequently exposed to steam at a fixed temperature and pressure for a fixed time.

Abstract: Saturation variations are obtained by displacing a first fluid (for example water) that initially saturates a sample (1) coated with resin (2) by injecting therein, through a first end plate or cap (3) and by means of a pump (7), a second fluid (for example oil). The mixture flowing out through an opposite end plate (4) is collected in an initially filled two-phase separator (9) placed on an electronic balance (10). The first excess fluid flows towards a vessel (13), and the progressive accumulation of the second fluid in separator (9) leads to a variation in the total weight. A programmed processor (14) computes permanently the saturation values of the sample with respect to the first and to the second fluid, from the measured weight variations of separator (9). The method and device can be used for laboratory measurements of rock samples for example.

Abstract: A method of compensating for load/environment temperature differential-induced measured load weight error comprises the steps of: providing a load having a load temperature T.sub.L ; providing an environment having an environment temperature T.sub.E, different from the load temperature; subjecting the load to the environment at time t.sub.0 ; measuring the weight w.sub.0 of the load at time t.sub.0 ; measuring the weight w.sub.1 of the load at time t.sub.1 ; and calculating the change in weight .DELTA.w.sub.td of the load, between the time t.sub.0 at which the load is subjected to the environment and the time t.sub.2 at which the load and environment temperatures reach equilibrium, induced by the temperature differential between the load and the environment, from the measured load weights w.sub.0 and w.sub.1. The method further comprises the steps of: measuring the weight w.sub.n of the load at time t.sub.n .gtoreq.t.sub.2 ; and subtracting the temperature differential-induced load weight change .DELTA.w.sub.

Abstract: On a slab-like board formed of a transparent material is closely attached a wedge-shaped transparent cover member provided with a recess in a central inner portion, thereby to form a clearance. The height of the clearance between the recess and the board is configured to decrease continuously or in steps. When an immunological active substance such as a monoclonal antibody is caused to sensitize carrier particles F, and a reagent having the carrier particles F dispersed into a liquid medium mainly composed of the water is mixed with a specimen, the reaction will occur in which the flocculate is formed from plural carrier particles. When this reaction liquid is poured into the clearance through the opening, the reaction liquid penetrates in the direction having a narrower vertical spacing due to surface tension. A single carrier particle unflocculated can move deep within the recess because it is small in diameter, but the flocculate G is trapped on its way and can not move because of its size.

Abstract: A sensor for detecting the presence of a particular chemical by determining the absolute frequency shift in the oscillating frequency of an antibody-coated oscillator. Specific antibodies deposited on a high Q crystal oscillator detect the change in frequency as chemical particulates become trapped by the antibodies and change the effective mass of the crystal. In one embodiment, two oscillating crystals are used, one that has been coated with the antibodies, and one that is uncoated. This permits detection of frequency differences between the oscillating frequencies of the two crystals, thus eliminating pressure, temperature, and humidity corrections that conventionally must be made. The sensor maintains a high specificity by using antibodies that are specifically related to the chemical to be detected, while achieving relatively good sensitivity by using high Q oscillators, such as quartz or sapphire, and eliminating drift problems due to temperature, pressure, and humidity.

Abstract: The invention relates to a piezoelectric biosensor device and also to a method and a system utilizing a piezoelectric biosensor device for detecting metabolic growth requirements, antibiotic responses, and the specific bacterial products of microorganisms. When a microorganism is grown in an appropriate nutrient medium containing a metabolic product responsive polymer, metabolic products of the organism acidify the medium and precipitate a polymer metabolic product complex which deposits or accumulates on the surface of a piezoelectric biosensor device. The mass change on the surface of the device resulting from this deposit produces a change in the resonant frequency of the piezoelectric biosensor device which can be used to determine the growth and type of microorganism.

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: A gravimetric method for determining the iodine adsorption number of carbon black is disclosed. The concentration of an accurately weighed iodine solution is determined by titrating with a standardized titrant and determining the concentration of the iodine solution by the weight of the standardized titrant needed to reach the titration endpoint. An appropriate amount of accurately weighed iodine solution is mixed with an accurately weighed amount of carbon black, and the mixture is equilibrated. The concentration of the resulting supernatant is determined by determining the weight of the standardized titrant needed to reach the titration endpoint. The iodine adsorption number is then determined based on the gravimetrically determined concentrations of the solutions. Preferably, the method is semi-or fully automated, and an apparatus for accomplishing the same is disclosed.

Abstract: The present invention is a method of rapidly and reproducibly checking the quality of zirconium base material welds and heat affected zones. In this method, weldment samples are immersed in an elevated temperature fused salt bath for a time period sufficient, at the bath temperature selected, to produce an essentially black oxide film in acceptable quality welds while producing a scaling oxide in unacceptable welds.

Abstract: An apparatus and method for quantitatively measuring volatiles, solids and solvent extractables is described which provides rapid and accurate determinations using microwave heating, electronic balance weighing and solvent extracting of solubles. The method involves subjecting a weighed sample to microwave drying for a preselected time, reweighing to obtain the dry weight and determine volatile loss, solvent extracting the dried sample to determine fats, oils and other extractables followed by final measurement of residual solids. The apparatus is preferably automated to sequentially actuate the required weighing, microwave heating, solvent extraction, redrying, reweighing and calculation of the percentages of volatiles, solvent solubles and solids. The apparatus and method are particularly suited for analytical uses in the food and dairy industries.

Abstract: Method for measuring particulates in flue gas streams containing chemicals reactive with trace elements in the filters is disclosed which features pretreating the filters with chemicals comparable to those in the process stream whereby the reactions are completed prior to the measurement step, in particular, prior to establishment of the tare weight of said filter.

Abstract: A novel method of determining the portion of a given dairy cow feedstuff which is attributable to non-structural carbohydrates is disclosed. The method includes the steps of analytically determining the percentages of crude protein, lipid and ash in the dry matter concentration of a first feed sample, and in the neutral detergent fiber which has been separated from the soluble matter of a second sample of the same feed, and subtracting the amounts of crude protein, lipid and ash in the neutral detergent fiber from the respective amounts of the same substances in the original sample. The three difference figures are totaled and subtracted from the percentage of the second sample represented by neutral detergent solubles, i.e., 100 minus neutral detergent fiber, thereby providing an accurate indication of the percentage of non-structural carbohydrate in the feedstuff.

Abstract: Means for discriminating the corrosion susceptibility of alloys of zirconium in an environment of a water cooled, nuclear fission reactor.

Abstract: A method of quantitatively determining the amount of exposure of an object to ethylene oxide gas. A pre-weighed ethylene oxide-permeable container, which encloses a predetermined amount of catalyst for the reaction of the ethylene oxide gas to form a liquid, is placed adjacent to the object. The object and container are then exposed to ethylene oxide gas for controlled time and at a known humidity and temperature. The container is then reweighed. The weight gain of the container is a quantitative indication of the amount of exposure to ethylene oxide gas. The test system may be calibrated against its effect in known concentrations of ethylene oxide gas, so that the precise amount of exposure to ethylene oxide gas can be determined.

Abstract: A method for thermogravimetrically analyzing a plastic molding composition comprising carbon black and a vinyl chloride homopolymer or copolymer molding resin to determine the carbon black content wherein the method comprises the steps of compounding the molding composition so that the carbon black is uniformly dispersed therein, heating the molding composition in an inert atmosphere to a temperature sufficient to reproducibly thermally decompose the vinyl chloride homopolymer or copolymer, maintaining the molding composition at the decomposition temperature in an inert atmosphere for a first given time which is long enough so that there is no further significant weight loss, weighing the molding composition to determine the weight loss during the first given time and comparing the weight loss for the first given time with that for samples of known composition analyzed under the same conditions to determined the carbon black content of the molding composition.