Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry最新文献

{"title":"Measurement of Melting Point and Radiance Temperature (at Melting Point and at 653 nm) of Hafnium-3 (wt. %) Zirconium by a Pulse Heating Method.","authors":"A Cezairliyan, J L McClure","doi":"10.6028/jres.080A.065","DOIUrl":"10.6028/jres.080A.065","url":null,"abstract":"<p><p>A subsecond duration pulse heating method is used to measure the melting point and radiance temperature (at 653 nm) at the melting point of hafnium containing 3.12 weight percent zirconium. The results yield a value of 2471 K for the melting point on the International Practical Temperature Scale of 1968. The radiance temperature (at 653 nm) of this material at its melting point is 2236 K, and the corresponding normal spectral emittance is 0.39. Estimated inaccuracies are: 10 K in the melting point and in the radiance temperature, and 5 percent in the normal spectral emittance.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"659-662"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293532/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757479","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Calibration of Reflectance Standards.","authors":"W Budde","doi":"10.6028/jres.080A.057","DOIUrl":"10.6028/jres.080A.057","url":null,"abstract":"<p><p>Measurements of the diffuse spectral reflectance are usually not made as direct measurement of the incident and the reflected radiant flux but rather as measurements relative to a standard of known reflectance value. For the calibration of such standards, different methods have been described in the literature: Goniophotometric methods, also called Indicatrix methods or point-by-point methods.Methods based on the Kubelka-Munk theory.Integrating sphere methods according to Taylor, Benford, Sharp-Little, van den Akker, Korte. Various materials such as magnesium oxide, barium sulfate or opal glass are being used as standards. Their suitability as transfer or as working standards will be discussed. The results of comparative measurements between some of these methods will be given.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"585-595"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293524/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37758486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Diffuse Reflectance Spectroscopy; Applications, Standards, and Calibration (With Special Reference to Chromatography).","authors":"R W Frei","doi":"10.6028/jres.080A.055","DOIUrl":"https://doi.org/10.6028/jres.080A.055","url":null,"abstract":"<p><p>The multitude of areas in which diffuse reflectance spectroscopy can be applied has been described in several books and reviews and ranges from color measurements of textiles, pharmaceuticals, building materials, paper and pulp materials etc., to adsorption studies and other basic investigations in physical, inorganic and organic chemistry. The major area of application is still the measurement of color which has become indispensible in the quality control of colored products, dyes and pigments. Color matching practices and techniques with sophisticated instrumentation which can be fully computerized as well as the use of simpler filter instruments for quality control are mentioned. Transferability of reflectance data i.e., color coordinates, depends on the quality of standards particularly when absolute measurements are desired. The difficulty of finding suitable \"white standards\" with good reflection properties at low UV and with a good long term stability is discussed. Similar arguments hold for sphere coating materials. For the measurement of fluorescing surfaces suitable standards are lacking which renders transfer of such data almost impossible. The usefulness of diffuse reflectance techniques to study adsorption phenomena on small particle adsorbents is demonstrated with a malachite green-<i>o</i>-carboxylic acid lactone system studied by Kortüm. This or similar systems could be adopted to the measurement of relative surface areas on certain chromatographic adsorbents yielding more realistic values than the BET-method. The most recent area of application has been in the field of chromatography for the in situ evaluation of chromatographic zones in flat-bed chromatography, electrophoresis and isoelectric focusing. In chromatography, standardization is less problematic since usually relative measurements are sufficient. On the other hand one has to find suitable calibration procedures. The use of the Kubelka-Munk function is often questionable since we are usually not dealing with layers of infinite thickness and below 300 nm the conventional adsorbents such as silica gel, alumina or cellulose are strongly absorbing. Experiences with a new function combining the laws of Kubelka-Munk and Lambert-Beer are therefore presented. The problem is also to find calibration techniques which account for chromatographic parameters. Until recently it was believed that a quantitative evaluation of chromatograms required a number of reference zones to be developed on the same chromatogram. In our experience this is no longer true. A novel calibration technique which utilizes the concept of transferable calibration factors is discussed. With this approach a quantitative evaluation of a chromatogram with only one reference spot is possible. Here again scanning and data acquisition can be fully automated. The application of proper calibration procedures to differential reflectance techniques and the measurement of multi-component systems is briefly menti","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"551-565"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293522/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37758484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Interpretation of Diffuse Reflectance Spectra.","authors":"Harry G Hecht","doi":"10.6028/jres.080A.056","DOIUrl":"https://doi.org/10.6028/jres.080A.056","url":null,"abstract":"<p><p>Numerous treatments of the diffuse reflecting properties of scattering media have been described. Many theories give an adequate account of the reflectance for a specific set of conditions for which the model was constructed and the solution tested experimentally. Only those models which are considered to be fairly general are considered here. It is convenient to divide the theories into those based upon continuum models and those based upon statistical models. The continuum models typically describe the scattering and absorbing properties of a given medium in terms of two phenomenological constants. These models may all be regarded as varying levels of approximate solution to the general equation of radiative transfer. This provides a convenient basis for comparison of the various theories. The statistical models are based upon a summation of transmittances and reflectances from individual layers or particles. Thus, some assumptions must be made about the nature of the fundamental units, and the validity of the ultimate result will depend upon how closely these assumptions correspond with reality. Only the statistical models lead to expressions from which absolute absorptivities and scattering coefficients can be calculated and related to the actual particle characteristics. The relationship between the various models will be discussed and the features which typify the absorptivity and scattering coefficient according to each will be compared and related to the available experimental data. This leads to a consideration of the characteristics of appropriate model systems and standards.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"567-583"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293523/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37758485","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Acidic Potassium Dichromate Solutions as Ultraviolet Absorbance Standards.","authors":"R W Burke, R Mavrodineanu","doi":"10.6028/jres.080A.062","DOIUrl":"10.6028/jres.080A.062","url":null,"abstract":"<p><p>The absorbances of five concentrations of potassium dichromate in 0.001 <i>M</i> perchloric acid have been determined at eight wavelengths in the ultraviolet on the National Bureau of Standards Institute for Materials Research high-accuracy spectrophotometer. Four of the wavelengths-235, 257, 313, and 350 nm-correspond to absorbance maxima or minima in the HCrO₄ ^- spectrum and are useful wavelengths for checking the accuracy of the absorbance scale of narrow bandpass spectrophotometers. Although partial dimerization of HCrO₄ ^- to Cr₂O₇ ⁼ produces small positive deviations from Beer's law at these wavelengths, the apparent absorptivities calculated for each concentration are reproducible to one part in a thousand. The estimated uncertainties in the absorptivity values are ± 0.7 percent at 0.1 absorbance (<i>A</i>) and ± 0.2 percent near <i>A</i> = 1. These uncertainties include all known sources of possible systematic error and the 95 percent confidence level for the mean. The remaining four wavelengths used for measurement are near two predicted isosbestic points in the HCr0₄ ^-/Cr₂O₇ ⁼ spectra. The absorptivities at 345 nm are sufficiently independent of concentration that this wavelength can be used for checking absorbance linearity to one part in a thousand over the range <i>A</i> = 0.2-1.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"631-636"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293529/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Structure-Related Optical Characteristics of Thin Metallic Films in the Visible and Ultraviolet.","authors":"H E Bennett,&nbsp;J L Stanford","doi":"10.6028/jres.080A.064","DOIUrl":"https://doi.org/10.6028/jres.080A.064","url":null,"abstract":"Surface irregularities and crystalline order strongly influence both the scattered light and absorption of metallic films. These effects extend through all spectral regions but are particularly important in the visible and ultraviolet. Scattered light arises from several scattering mechanisms. Macroscopic irregularities such as dust, scratches and particulates are typically much less important than are microirregularities only a few tens of angstroms in height but covering the entire surface. For metals such as silver and aluminum, which have plasma edges in the ultraviolet, the excitation of surface plasmons resulting from these microirregularities causes additional incoherently reemitted or “scattered” light. Surface plasmon excitation also causes increased absorption in some wavelength regions. These effects are enhanced by dielectric overcoating layers, which both increase the absorption and scattering and shift the wavelength at which the peak occurs. Surface plasmon excitation is particularly important in the ultraviolet region, where the dielectric overcoating applied to prevent formation of an oxide film on aluminized mirrors, for example, can significantly change the mirror reflectance. Plasmon excitation is made possible by a momentum conserving process associated with material inhomogeneities and hence can presumably be caused by crystalline disorder in the metal surface as well as surface irregularities. If the disorder is present on a sufficiently fine scale, it also affects the band structure of the metal and hence its optical absorption. Examples of the effect of film structure on the optical properties of evaporated and sputtered metal films will be given.","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"643-658"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293531/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Nationwide Survey of ⁶⁰Co Teletherapy Dosimetry.","authors":"Marqarete Ehrlich, Garv L Welter","doi":"10.6028/jres.080A.066","DOIUrl":"10.6028/jres.080A.066","url":null,"abstract":"<p><p>The National Bureau of Standards is performing a study of the ability of radiation-therapy departments to deliver prescribed absorbed doses of ⁶⁰Co gamma radiation to a water phantom. Batches of thermoluminescence dosimeters are mailed to participating therapy departments for irradiation under prescribed conditions. Upon return of the dosimeters, the participants' computations are checked and the absorbed dose is evaluated from dosimeter response. The rugged dosimetry system was assembled mainly from commercial components adapted to the present requirements of relatively high flexibility of readout parameters and data-handling techniques, and of relatively high accuracy. The uncertainty in the dose interpretation inherent in the system is estimated to be about 4 percent. In order to illustrate the type of information that can be obtained from such a study, results of the first four mailings involving tests on 114 ⁶⁰Co gamma-ray beams are discussed. They show about 75 percent of the dose interpretations to be within 5 percent of the prescribed absorbed dose, and about 20 percent to be within 5 to 10 percent of this dose. Four dose interpretations showed discrepancies larger than 20 percent. Differences in the computations larger than 1 percent were observed in over one-half of the cases.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"663-668"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293533/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Errors in Spectrophotometry and Calibration Procedures to Avoid Them.","authors":"A G Reule","doi":"10.6028/jres.080A.060","DOIUrl":"10.6028/jres.080A.060","url":null,"abstract":"<p><p>Based on simple principles, spectrophotometry nevertheless demands a lot of precautions to avoid errors. The following properties of spectrophotometers will be discussed together with methods to test them: Spectral properties-wavelength accuracy, bandwidth, stray light; photometric linearity; interactions between sample and instrument-multiple reflections, polarization, divergence, sample wedge, sample tilt, optical path length (refractive index), interferences. Calibration of master instruments is feasible only by complicated procedures. With such a master instrument standards may be calibrated which greatly simplify performance checks of instruments used for practical work. For testing high quality spectrophotometers the use of emission lines and nearly neutral absorbing solid filters as standards seems to be superior, for some kinds of routine instruments the use of absorption bands and liquid filters may be necessary.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"609-624"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293527/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37758488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Some Methods of Luminescence Efficiency Measurements.","authors":"Alfred Bril,&nbsp;A Willy de Jager-Veenis","doi":"10.6028/jres.080A.039","DOIUrl":"https://doi.org/10.6028/jres.080A.039","url":null,"abstract":"<p><p>Methods of absolute and relative radiant and quantum efficiency measurements are described for ultraviolet, visible, cathode-ray, and x-ray excitations. Data on some standard luminescent materials are given.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 3","pages":"401-407"},"PeriodicalIF":0.0,"publicationDate":"1976-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293346/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757627","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The International Practical Temperature Scale of 1968 in the Region 90.188 K to 903.89 K as Maintained at the National Bureau of Standards.","authors":"George T Furukawa, John L Riddle, William R Bigge","doi":"10.6028/jres.080A.053","DOIUrl":"10.6028/jres.080A.053","url":null,"abstract":"<p><p>The reproducibility of the International Practical Temperature Scale of 1968 (IPTS-68) in the region 90.188 K to 903.89 K as maintained at the National Bureau of Standards is discussed. The realizations of the triple point of water, the freezing points of zinc and tin, and the boiling point of oxygen are described. The average of the standard deviations of the resistance measurements at the triple point of water of 213 platinum resistance thermometers received for calibration over a two-year period corresponds to ±0.15 mK. The standard deviations of the resistance ratio <i>R</i>(<i>T</i>)/<i>R</i>(0°C) obtained with check thermometers employed for monitoring the zinc, tin, and oxygen point measurements correspond to ±0.28 mK, ±0.30 mK, and ±0.16 mK, respectively; the results of repeated calibrations with five thermometers show comparable reproducibility at the tin and oxygen points but the reproducibility is worse by a factor of two at the zinc point. When suitably packed for protection from possible mechanical shock platinum resistance thermometers can be shipped by common carrier and retain their calibrations.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 3","pages":"477-504"},"PeriodicalIF":0.0,"publicationDate":"1976-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293354/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37758482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}