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Gordon, W. A.

Publications and source records attributed to Gordon, W. A..

At least 19 records

Development of a drift-correction procedure for a photoelectric spectrometer

A technique has been developed to automatically correct for drifts in the radiometric sensitivity of the detector channels in a direct-reading emission spectrometer. The method utilizes a 1000 W tungsten-halogen reference lamp to illuminate the detectors through the same optical path as that traversed during the analysis of the sample. Detector channel responses to the light are compared to those for the same light intensity at the time of analytical calibration. This corrects for the drift. It is noted that with the exception of positioning the lamp, the procedure is fully automatic.

Chapman, G. B., II

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

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.

Chapman, G. B., II

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

This paper describes a study of matrix effects related to the chemical form of materials analyzed. The study was made using an arc in argon 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. Among these, 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 pressure of the solid materials placed on the anodes and dissociation reactions of the molecules in the gaseous environment.

Gordon, W. A.

Sample preparation of metal alloys by electric discharge machining

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.

Chapman, G. B., II

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

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.

Gordon, W. A.

Quantitation and detection of vanadium in biologic and pollution materials

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.

Gordon, W. A.

Determination of work functions near melting points of refractory metals by using a direct-current arc.

A direct-current arc in argon at atmospheric pressure was used to determine effective work functions of refractory metals, including tantalum, tungsten, molybdenum, and niobium. The procedure is experimentally advantageous, because surface cleanliness of the specimen is not critical, high vacuum is not required, and the anode-cathode spacing is not critical. The experimental procedure involves striking an arc to a metal wire cathode to form a melted ball having an emitting area defined by its diameter. The literature melting point of the metal is taken as the emitting temperature. By using these parameters and the known arc current, effective work functions were calculated from the Richardson-Dushman equation. The calculated work functions agree with recommended handbook values to within about 0.1 V and have typical repeatabilities of 0.02 V.

Gordon, W. A.

Determination of work functions near melting points of refractory metals by using a direct-current arc

Effective work functions of refractory metals at temperatures near their melting points were determined by using a direct-current arc. A metal wire connected as the cathode was melted by striking an arc discharge in an argon atmosphere. A melted sphere was formed with a definite emitting area which was calculated from the sphere diameter measured after terminating the arc. Effective work functions were calculated from the Richardson-Dushman equation by using this emission area. The procedure is experimentally advantageous because surface cleanliness of the specimen is not critical, high vacuum is not required, and the anode-cathode spacing is not critical.

Gordon, W. A.

Evaluation of some wide dynamic range readout systems for photoelectric integrating spectrometers

Five types of electronic circuits commonly used for readout of currents from photomultiplier tubes were evaluated. This evaluation was conducted to define the experimental limits of achieving the widest possible dynamic range of light detection and concentration measurements in spectrochemical analysis. The circuits evaluated included the photon-counting technique and four dc circuits. These circuits displayed a dynamic range from 3 to about 4.5 decades within a repeatability criterion of 1 percent, or better. The maximum dynamic range allowed by the photomultiplier tube in this application was estimated to be about 6 decades.

Franklin, M. L.

Simplified procedure for emission spectrochemical analysis

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.

Gordon, W. A.

Control apparatus for spectral energy source

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.

Gordon, W. A.