39,998 research outputs found

    Arc electrode of graphite with ball tip Patent

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    Arc electrode of graphite with tantalum ball ti

    Simplified procedure for emission spectrochemical analysis

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    Procedure involves dissolution of samples to prepare them for analysis, and uses single set of experimental conditions to analyze wide variety of materials and compositions without compromising analysis accuracy. Automated spectrometer alloys per sample analysis time of four minutes after sample dissolution

    Control apparatus for spectral energy source

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    Automatic light-controlling system for dc arc emission spectrographs controls the vaporization rate of the sample and stabilizes the dc arc. The output energy is regulated such that advantage can be taken of the highly sensitive dc arc source without sacrificing the desired precision

    Quantitation and detection of vanadium in biologic and pollution materials

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    A review is presented of special considerations and methodology for determining vanadium in biological and air pollution materials. In addition to descriptions of specific analysis procedures, general sections are included on quantitation of analysis procedures, sample preparation, blanks, and methods of detection of vanadium. Most of the information presented is applicable to the determination of other trace elements in addition to vanadium

    Emission spectrometric arcing procedure with minimal effect of chemical form of sample

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    Matrix effects related to the chemical form of analyzed materials were studied. An arc in argon was used which was buffered with silver chloride. The effect of chemical form was minimal for a variety of metals, oxides, and carbides representing the most refractory compounds and thermally stable metal-containing molecules. Only four of the most refractory materials known showed significant emission depressions due to incomplete volatilization in the arc system. These results are discussed in terms of vapor pressures of the solid materials placed on the anodes and dissociation reactions of the molecules in the gaseous environment

    Automatic data processing for photographic photometry in spectrographic analysis

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    Automatic data processing for photographic photometry in spectrographic analysi

    Phase perturbation measurements through a heated ionosphere

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    High frequency radiowaves incident on an overdense (i.e., HF-frequency penetration frequency) ionosphere produce electron density irregularities. The effect of such ionospheric irregularities on the phase of UHF-radiowaves was determined. For that purpose the phase of radiowaves originating from celestial radio sources was observed with two antennas. The radiosources were chosen such that the line of sight to at least one of the antennas (usually both) passed through the modified volume of the ionosphere. Observations at 430 MHz and at 2380 MHz indicate that natural irregularities have a much stronger effect on the UHF phase fluctuations than the HF-induced irregularities for presently achieved HF-power densities of 20-80 uW/sq m. It is not clear whether some of the effects observed are the result of HF-modification of the ionosphere. Upper limits on the phase perturbations produced by HF-modification are 10 deg at 2380 MHz and 80 deg at 430 MHz

    Sample preparation of metal alloys by electric discharge machining

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    Electric discharge machining was investigated as a noncontaminating method of comminuting alloys for subsequent chemical analysis. Particulate dispersions in water were produced from bulk alloys at a rate of about 5 mg/min by using a commercially available machining instrument. The utility of this approach was demonstrated by results obtained when acidified dispersions were substituted for true acid solutions in an established spectrochemical method. The analysis results were not significantly different for the two sample forms. Particle size measurements and preliminary results from other spectrochemical methods which require direct aspiration of liquid into flame or plasma sources are reported

    Development of a drift-correction procedure for a direct-reading spectrometer

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    A procedure which provides automatic correction for drifts in the radiometric sensitivity of each detector channel in a direct-reading emission spectrometer is described. Such drifts are customarily controlled by the regular analyses of standards, which provide corrections for changes in the excitational, optical, and electronic components of the instrument. This standardization procedure, however, corrects for the optical and electronic drifts. It is a step that must be taken if the time, effort, and cost of processing standards is to be minimized. This method of radiometric drift correction uses a 1,000-W tungsten-halogen reference lamp to illuminate each detector through the same optical path as that traversed during sample analysis. The responses of the detector channels to this reference light are regularly compared with channel response to the same light intensity at the time of analytical calibration in order to determine and correct for drift. Except for placing the lamp in position, the procedure is fully automated and compensates for changes in spectral intensity due to variations in lamp current. A discussion of the implementation of this drift-correction system is included
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