Pub Date : 1976-09-01Epub Date: 1976-10-01DOI: 10.6028/jres.080A.071
Arnold Wexler
In 1971 Wexler and Greenspan published a formulation for the vapor pressure of water encompassing the temperature range 0 to 100 °C. In this paper a revision is made of that earlier formulation to make it consistent with the definitive experimental value of the vapor pressure of water at its triple point recently obtained by Guildner, Johnson, and Jones. The two formulations are essentially identical at temperatures from 25 to 100 °C. For temperatures below 25 °C the new formulation predicts values that are higher than the 1971 formulation. At the triple point, the vapor pressure given by the new formulation is 611.657 Pa whereas the value given by the 1971 formulation is 611.196 Pa. A table is given of the vapor pressure as a function of temperature at 0.1-deg intervals over the range 0 to 100 °C on the International Practical Temperature Scale of 1968, together with values of the temperature derivative at 1-deg intervals.
1971 年,韦克斯勒和格林斯潘发表了水蒸气压的计算公式,涵盖了 0 到 100 °C 的温度范围。本文对之前的公式进行了修订,使其与 Guildner、Johnson 和 Jones 最近获得的水在三相点时的蒸气压的最终实验值保持一致。这两个公式在 25 至 100 °C 的温度范围内基本相同。在温度低于 25 °C 时,新公式的预测值高于 1971 年的公式。在三相点上,新配方给出的蒸气压为 611.657 Pa,而 1971 年配方给出的值为 611.196 Pa。
{"title":"Vapor Pressure Formulation for Water in Range 0 to 100 °C. A Revision.","authors":"Arnold Wexler","doi":"10.6028/jres.080A.071","DOIUrl":"10.6028/jres.080A.071","url":null,"abstract":"<p><p>In 1971 Wexler and Greenspan published a formulation for the vapor pressure of water encompassing the temperature range 0 to 100 °C. In this paper a revision is made of that earlier formulation to make it consistent with the definitive experimental value of the vapor pressure of water at its triple point recently obtained by Guildner, Johnson, and Jones. The two formulations are essentially identical at temperatures from 25 to 100 °C. For temperatures below 25 °C the new formulation predicts values that are higher than the 1971 formulation. At the triple point, the vapor pressure given by the new formulation is 611.657 Pa whereas the value given by the 1971 formulation is 611.196 Pa. A table is given of the vapor pressure as a function of temperature at 0.1-deg intervals over the range 0 to 100 °C on the International Practical Temperature Scale of 1968, together with values of the temperature derivative at 1-deg intervals.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 5-6","pages":"775-785"},"PeriodicalIF":0.0,"publicationDate":"1976-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312760/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757861","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}
Pub Date : 1976-09-01Epub Date: 1976-10-01DOI: 10.6028/jres.080A.068
L A Guildner, R E Edsinger
The range over which thermodynamic temperatures have been realized by gas thermometry at the NBS has been extended to 730 K. The results are preserved by measuring the corresponding international practical temperatures. The difference between them is expressed as the following polynomial: which is valid in the range 273 to 730 K. The difference found and the estimated uncertainties at the three defining fixed points in the range covered are [Table: see text].
通过测量相应的国际实用温度,结果得以保留。它们之间的差值用以下多项式表示: T / K - T 68 / K 68 = - 120 , 887.784 / T 68 2 + 1213.53295 / T 68 - 4.3159552 + 6.44075647 × 10 - 3 T 68 - 3.56638846 × 10 - 6 T 68 2,在 273 至 730 K 范围内有效。
{"title":"Deviation of International Practical Temperatures from Thermodynamic Temperatures in the Temperature Range from 273.16 K to 730 K.","authors":"L A Guildner, R E Edsinger","doi":"10.6028/jres.080A.068","DOIUrl":"10.6028/jres.080A.068","url":null,"abstract":"<p><p>The range over which thermodynamic temperatures have been realized by gas thermometry at the NBS has been extended to 730 K. The results are preserved by measuring the corresponding international practical temperatures. The difference between them is expressed as the following polynomial: <dispformula> <math><mrow><mi>T</mi> <mo>/</mo> <mi>K</mi> <mo>-</mo> <msub><mi>T</mi> <mrow><mn>68</mn></mrow> </msub> <mo>/</mo> <msub><mi>K</mi> <mrow><mn>68</mn></mrow> </msub> <mo>=</mo> <mo>-</mo> <mn>120</mn> <mo>,</mo> <mn>887.784</mn> <mo>/</mo> <msubsup><mi>T</mi> <mrow><mn>68</mn></mrow> <mn>2</mn></msubsup> <mo>+</mo> <mn>1213.53295</mn> <mo>/</mo> <msub><mi>T</mi> <mrow><mn>68</mn></mrow> </msub> <mo>-</mo> <mn>4.3159552</mn> <mo>+</mo> <mn>6.44075647</mn> <mo>×</mo> <msup><mrow><mn>10</mn></mrow> <mrow><mo>-</mo> <mn>3</mn></mrow> </msup> <msub><mi>T</mi> <mrow><mn>68</mn></mrow> </msub> <mo>-</mo> <mn>3.56638846</mn> <mo>×</mo> <msup><mrow><mn>10</mn></mrow> <mrow><mo>-</mo> <mn>6</mn></mrow> </msup> <msubsup><mi>T</mi> <mrow><mn>68</mn></mrow> <mn>2</mn></msubsup> </mrow> </math> </dispformula> which is valid in the range 273 to 730 K. The difference found and the estimated uncertainties at the three defining fixed points in the range covered are [Table: see text].</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 5-6","pages":"703-738"},"PeriodicalIF":0.0,"publicationDate":"1976-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312757/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757426","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}
Pub Date : 1976-09-01Epub Date: 1976-10-01DOI: 10.6028/jres.080A.070
J L Waring, R S Roth, H S Parker, W S Brower
Phase equilibrium diagrams have been constructed from experimental data for the systems Sb2O4-NaSbO3, Sb2O4-KSbO3, and Sb2O4-NaSbO3-NaF. The system Sb2O4-NaSbO3 contains only an intermediate pyrochlore type solid solution with a maximum melting point of 1490 °C at a Na:Sb atom ratio of 3:5. The Sb2O4-KSbO3 system contains in addition to the pyrochlore phase a compound 3K2O • 5Sb2O5 which melts congruently at about 1450 °C and two polymorphs of K2O • 2Sb2O5. The low temperature form of K2O • 2Sb2O5 was found to be monoclinic P21/c with a = 7.178, b = 13.378, c = 11.985 A, β = 124°10'. The melting point of Sb2O4 was found to be 1350 ± 5 °C and NaSbO3 and KSbO3 both melt congruently at 1555 ± 5 °C and 1410 ± 5 °C respectively. The previously reported cubic form of KSbO3 was found to be a K+ deficient phase stabilized by reaction with atmospheric moisture. A similar cubic phase which appears to be a good Na+ ion conductor can be synthesized in the ternary system NaSbO3-Sb2O4-NaF.
利用实验数据建立了Sb2O4-NaSbO3、Sb2O4-KSbO3和Sb2O4-NaSbO3- naf体系的相平衡图。在Na:Sb原子比为3:5的条件下,Sb2O4-NaSbO3体系仅含中间焦绿盐型固溶体,最大熔点为1490℃。在Sb2O4-KSbO3体系中,除焦绿石相外,还含有在1450℃时完全熔化的化合物3K2O•5Sb2O5和两种K2O•2Sb2O5的多晶相。K2O•2Sb2O5的低温形态为单斜晶型P21/c, a = 7.178, b = 13.378, c = 11.985 a, β = 124°10′。Sb2O4的熔点为1350±5℃,NaSbO3和KSbO3的熔点分别为1555±5℃和1410±5℃。先前报道的立方形式的KSbO3被发现是与大气湿度反应稳定的K+缺乏相。在三元体系NaSbO3-Sb2O4-NaF中可以合成一种类似的立方相,它似乎是Na+离子的良好导体。
{"title":"Phase Equilibria and Crystal Growth in the Alkali Antimonate Systems Sb<sub>2</sub>O<sub>4</sub>-NaSbO<sub>3/</sub> Sb<sub>2</sub>O<sub>4</sub>-KSbO<sub>3/</sub>, and Sb<sub>2</sub>O<sub>4</sub>-NaSbO<sub>3</sub>-NaF.","authors":"J L Waring, R S Roth, H S Parker, W S Brower","doi":"10.6028/jres.080A.070","DOIUrl":"https://doi.org/10.6028/jres.080A.070","url":null,"abstract":"<p><p>Phase equilibrium diagrams have been constructed from experimental data for the systems Sb<sub>2</sub>O<sub>4</sub>-NaSbO<sub>3</sub>, Sb<sub>2</sub>O<sub>4</sub>-KSbO<sub>3</sub>, and Sb<sub>2</sub>O<sub>4</sub>-NaSbO<sub>3</sub>-NaF. The system Sb<sub>2</sub>O<sub>4</sub>-NaSbO<sub>3</sub> contains only an intermediate pyrochlore type solid solution with a maximum melting point of 1490 °C at a Na:Sb atom ratio of 3:5. The Sb<sub>2</sub>O<sub>4</sub>-KSbO<sub>3</sub> system contains in addition to the pyrochlore phase a compound 3K<sub>2</sub>O • 5Sb<sub>2</sub>O<sub>5</sub> which melts congruently at about 1450 °C and two polymorphs of K<sub>2</sub>O • 2Sb<sub>2</sub>O<sub>5</sub>. The low temperature form of K<sub>2</sub>O • 2Sb<sub>2</sub>O<sub>5</sub> was found to be monoclinic P2<sub>1</sub>/c with <i>a</i> = 7.178, <i>b</i> = 13.378, <i>c</i> = 11.985 A, <i>β</i> = 124°10'. The melting point of Sb<sub>2</sub>O<sub>4</sub> was found to be 1350 <i>±</i> 5 °C and NaSbO<sub>3</sub> and KSbO<sub>3</sub> both melt congruently at 1555 ± 5 °C and 1410 ± 5 °C respectively. The previously reported cubic form of KSbO<sub>3</sub> was found to be a K<sup>+</sup> deficient phase stabilized by reaction with atmospheric moisture. A similar cubic phase which appears to be a good Na<sup>+</sup> ion conductor can be synthesized in the ternary system NaSbO<sub>3</sub>-Sb<sub>2</sub>O<sub>4</sub>-NaF.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 5-6","pages":"761-774"},"PeriodicalIF":0.0,"publicationDate":"1976-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312759/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757428","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}
Pub Date : 1976-09-01Epub Date: 1976-10-01DOI: 10.6028/jres.080A.072
C H Corliss, J L Tech
Mean radiative lifetimes for 408 energy levels of neutral iron are revised from our 1967 paper on the basis of comparison with 81 subsequently measured lifetimes. The standard deviation of the ratio of the revised values to the reference lifetimes is 30 percent.
{"title":"Revised Lifetimes of Energy Levels in Neutral Iron.","authors":"C H Corliss, J L Tech","doi":"10.6028/jres.080A.072","DOIUrl":"10.6028/jres.080A.072","url":null,"abstract":"<p><p>Mean radiative lifetimes for 408 energy levels of neutral iron are revised from our 1967 paper on the basis of comparison with 81 subsequently measured lifetimes. The standard deviation of the ratio of the revised values to the reference lifetimes is 30 percent.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 5-6","pages":"787-797"},"PeriodicalIF":0.0,"publicationDate":"1976-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312761/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757862","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}
Pub Date : 1976-09-01Epub Date: 1976-10-01DOI: 10.6028/jres.080A.069
Hans M Roder
The specific heats of saturated liquid ethane, Cσ , have been measured at 106 temperatures in the temperature range 93 to 301 K. The specific heats at constant volume, Cv have been measured at 19 densities ranging from 0.2 to 3.1 times the critical density, at temperatures between 91 and 330 K, with pressures to 33 MPa, at 200 PVT states in all. The uncertainty of most of the measurements is estimated to be less than 2.0 percent. As the critical point is approached the uncertainty rises to about 5.0 percent. The measurements were performed to provide input data for accurate calculations of the thermodynamic properties for ethane. They are believed to be the most comprehensive specific heat measurements available for the liquid and vapor states of ethane.
{"title":"Measurements of the Specific Heats, <i>C<sub>σ</sub></i> , and <i>C<sub>v</sub></i> of Dense Gaseous and Liquid Ethane<sup />.","authors":"Hans M Roder","doi":"10.6028/jres.080A.069","DOIUrl":"10.6028/jres.080A.069","url":null,"abstract":"<p><p>The specific heats of saturated liquid ethane, <i>C<sub>σ</sub></i> , have been measured at 106 temperatures in the temperature range 93 to 301 K. The specific heats at constant volume, <i>C<sub>v</sub></i> have been measured at 19 densities ranging from 0.2 to 3.1 times the critical density, at temperatures between 91 and 330 K, with pressures to 33 MPa, at 200 PVT states in all. The uncertainty of most of the measurements is estimated to be less than 2.0 percent. As the critical point is approached the uncertainty rises to about 5.0 percent. The measurements were performed to provide input data for accurate calculations of the thermodynamic properties for ethane. They are believed to be the most comprehensive specific heat measurements available for the liquid and vapor states of ethane.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 5-6","pages":"739-759"},"PeriodicalIF":0.0,"publicationDate":"1976-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312758/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757427","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}
Pub Date : 1976-07-01Epub Date: 1976-08-01DOI: 10.6028/jres.080A.058
John B Schutt
Applications for optical diffusers in space projects are presented which include the functions of reflection, transmittance, and collection. These modes encompass such diverse uses as temperature regulation and ozone concentration monitors. Discussed is the cooperative aspect of diffuse reflectance and environmental stability. Magnesium oxide, sodium chloride and barium sulphate are evaluated in some detail. The importance of scene scattering behavior to modeling the earth's radiation budget and in determining thermal inertias of the earth's surface are discussed, because solar albedo serves as the weighting function in the solar input irradiance. Finally, work in the area of canopy reflectance modeling is reviewed with verification data included whenever available. Some knowledge of the bidirectional reflectance properties of vegetation is necessary for identification, acreage computations, and scene transference.
{"title":"Understanding Bidirectional Reflectance and Transmission for Space Applications.","authors":"John B Schutt","doi":"10.6028/jres.080A.058","DOIUrl":"https://doi.org/10.6028/jres.080A.058","url":null,"abstract":"<p><p>Applications for optical diffusers in space projects are presented which include the functions of reflection, transmittance, and collection. These modes encompass such diverse uses as temperature regulation and ozone concentration monitors. Discussed is the cooperative aspect of diffuse reflectance and environmental stability. Magnesium oxide, sodium chloride and barium sulphate are evaluated in some detail. The importance of scene scattering behavior to modeling the earth's radiation budget and in determining thermal inertias of the earth's surface are discussed, because solar albedo serves as the weighting function in the solar input irradiance. Finally, work in the area of canopy reflectance modeling is reviewed with verification data included whenever available. Some knowledge of the bidirectional reflectance properties of vegetation is necessary for identification, acreage computations, and scene transference.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"597-603"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293525/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757474","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}
Pub Date : 1976-07-01Epub Date: 1976-08-01DOI: 10.6028/jres.080A.061
A R Robertson
In an instrument as complex as a spectrophotometer there are many potential sources of error. Because of this it is useful to have available standard materials whose spectral transmittances are known accurately. Periodic measurement of such standards provides a useful indication of whether a spectrophotometer is producing accurate results. If the spectral transmittance functions of these standards are chosen suitably, the measurements can provide diagnostic information to indicate what type of error is occurring. Among the factors that most often lead to errors in spectrophotometry are the slit-width, the wavelength scale, the photometric scale, and stray radiation. Suitable material standards can provide indications of the occurrence of these errors. However it is sometimes difficult to identify a particular error since often several errors will occur at the same time. Several sets of standards for testing spectrophotometers are available or can be constructed easily. Most of these are glass filters, but interference filters, perforated screens, and rotating sectors are also used. Liquid filters have some advantages, especially in the ultraviolet where glass filters absorb too strongly to be useful. However difficulties in preparing and handling liquid filters can introduce uncertainties. It is important that standard materials are insensitive to environmental conditions (such as temperature) and that they are stable over a long period of time. Unfortunately, many of the materials with the most suitable spectral characteristics are least suitable in these respects, and it would be very useful if new and better materials could be developed.
{"title":"Standardization in Transmission Spectrophotometry in the Visible and Ultraviolet Spectral Regions.","authors":"A R Robertson","doi":"10.6028/jres.080A.061","DOIUrl":"10.6028/jres.080A.061","url":null,"abstract":"<p><p>In an instrument as complex as a spectrophotometer there are many potential sources of error. Because of this it is useful to have available standard materials whose spectral transmittances are known accurately. Periodic measurement of such standards provides a useful indication of whether a spectrophotometer is producing accurate results. If the spectral transmittance functions of these standards are chosen suitably, the measurements can provide diagnostic information to indicate what type of error is occurring. Among the factors that most often lead to errors in spectrophotometry are the slit-width, the wavelength scale, the photometric scale, and stray radiation. Suitable material standards can provide indications of the occurrence of these errors. However it is sometimes difficult to identify a particular error since often several errors will occur at the same time. Several sets of standards for testing spectrophotometers are available or can be constructed easily. Most of these are glass filters, but interference filters, perforated screens, and rotating sectors are also used. Liquid filters have some advantages, especially in the ultraviolet where glass filters absorb too strongly to be useful. However difficulties in preparing and handling liquid filters can introduce uncertainties. It is important that standard materials are insensitive to environmental conditions (such as temperature) and that they are stable over a long period of time. Unfortunately, many of the materials with the most suitable spectral characteristics are least suitable in these respects, and it would be very useful if new and better materials could be developed.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"625-630"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293528/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757475","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}
Pub Date : 1976-07-01Epub Date: 1976-08-01DOI: 10.6028/jres.080A.067
Shu-Sing Chang
The principle of a self-balancing potentiometric system is described. The principle is applied to the modification of an existing manually operated thermo-free, low voltage potentiometer consisting of Diesselhorst ring elements. The modification involves the addition of reed relays which enable the potentiometer voltage to be set by digital signals. By incorporating a digital voltmeter, or an analog-to-digital converter, and a nanovolt amplifier with the modified potentiometer, self-balancing of the potentiometer may be achieved through either hardware logic implementation or direct digital control from a minicomputer. The resolution of this self-balancing potentiometric system for a full scale input of 100 mV is about one to 10 parts in 108. With real-time digital processing of the data, resolution of about 1 nV or better has been achieved for slowly changing input signals. The overall accuracy of the system is better than 10 ppm for voltage measurements and about 1 ppm for voltage ratio or resistance measurements.
{"title":"A Self-Balancing Nanovolt Potentiometric System for Thermometry and Calorimetry.","authors":"Shu-Sing Chang","doi":"10.6028/jres.080A.067","DOIUrl":"https://doi.org/10.6028/jres.080A.067","url":null,"abstract":"<p><p>The principle of a self-balancing potentiometric system is described. The principle is applied to the modification of an existing manually operated thermo-free, low voltage potentiometer consisting of Diesselhorst ring elements. The modification involves the addition of reed relays which enable the potentiometer voltage to be set by digital signals. By incorporating a digital voltmeter, or an analog-to-digital converter, and a nanovolt amplifier with the modified potentiometer, self-balancing of the potentiometer may be achieved through either hardware logic implementation or direct digital control from a minicomputer. The resolution of this self-balancing potentiometric system for a full scale input of 100 mV is about one to 10 parts in 10<sup>8</sup>. With real-time digital processing of the data, resolution of about 1 nV or better has been achieved for slowly changing input signals. The overall accuracy of the system is better than 10 ppm for voltage measurements and about 1 ppm for voltage ratio or resistance measurements.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"669-675"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293534/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37757480","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}
Pub Date : 1976-07-01Epub Date: 1976-08-01DOI: 10.6028/jres.080A.059
Gregory J Buffone
Light scattering methods for the physical analysis of synthetic and biological polymers necessitates the use of scattering standards and absolute light scattering measurements. Standardization has not been employed when light scattering has been used to monitor immunochemical reactions using a kinetic or thermodynamic mode. The concentration of a specific protein present in a complex matrix such as urine, serum or cerebrospinal fluid, is measured by reacting the protein of interest with its specific antibody and then measuring the excess light scattering of the solution produced by the formation of antigen antibody complexes. The lack of established light scattering standards in the area of immunochemical measurements makes instrumental quality control difficult and has hindered direct comparison of data among investigators. Both solid and liquid light scattering standards would be necessary to encompass the wide range of instrumentation currently in use. Several solid standards which have been used in the past include reflecting diffusers such as vitrolite, magnesium carbonate crystals with a ground surface, magnesium oxide coatings on magnesium carbonate crystal, casein paint on vitrolite, and solid opal glass transmitting diffusers such as flashed opal glass and solid opal glass. These standards, while applicable to manual light scattering photometers, are not suitable for recently developed automated instrumentation. Liquid standards in the form of Ludox®, solutions of polystyrene, suspensions of small diameter latex spheres and even pure organic solvents could be used more easily with the continuous flow and discrete automated analyzers. The introduction of instrumental standards at this level of analysis would result in improved overall quality control and facilitate data and method comparison between laboratories.
{"title":"Standardization of Light Scattering Measurement in Conjunction With Immunochemical Analysis.","authors":"Gregory J Buffone","doi":"10.6028/jres.080A.059","DOIUrl":"10.6028/jres.080A.059","url":null,"abstract":"<p><p>Light scattering methods for the physical analysis of synthetic and biological polymers necessitates the use of scattering standards and absolute light scattering measurements. Standardization has not been employed when light scattering has been used to monitor immunochemical reactions using a kinetic or thermodynamic mode. The concentration of a specific protein present in a complex matrix such as urine, serum or cerebrospinal fluid, is measured by reacting the protein of interest with its specific antibody and then measuring the excess light scattering of the solution produced by the formation of antigen antibody complexes. The lack of established light scattering standards in the area of immunochemical measurements makes instrumental quality control difficult and has hindered direct comparison of data among investigators. Both solid and liquid light scattering standards would be necessary to encompass the wide range of instrumentation currently in use. Several solid standards which have been used in the past include reflecting diffusers such as vitrolite, magnesium carbonate crystals with a ground surface, magnesium oxide coatings on magnesium carbonate crystal, casein paint on vitrolite, and solid opal glass transmitting diffusers such as flashed opal glass and solid opal glass. These standards, while applicable to manual light scattering photometers, are not suitable for recently developed automated instrumentation. Liquid standards in the form of Ludox<sup>®</sup>, solutions of polystyrene, suspensions of small diameter latex spheres and even pure organic solvents could be used more easily with the continuous flow and discrete automated analyzers. The introduction of instrumental standards at this level of analysis would result in improved overall quality control and facilitate data and method comparison between laboratories.</p>","PeriodicalId":17018,"journal":{"name":"Journal of Research of the National Bureau of Standards. Section A, Physics and Chemistry","volume":"80A 4","pages":"605-608"},"PeriodicalIF":0.0,"publicationDate":"1976-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293526/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37758487","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}
Pub Date : 1976-07-01Epub Date: 1976-08-01DOI: 10.6028/jres.080A.063
R Mavrodineanu
Various characteristics of evaporated metal-on-fused silica filters are discussed in relation to their optical transmission properties. Special metal holders provided with shutters were designed to be used with these filters, and are described in detail. Transmittance measurements, performed in various conditions, are reported and indicate that the evaporated metal-on-fused silica filters might present an acceptable material as transfer standards in spectrophotometry.
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