Compression curves of the cesium halides using murnaghan logarithmic equation

The pressure derivatives of the adiabatic bulk moduli of the cesium halides are evaluated from the pressure derivatives of their elastic constants C₁₁ and C₁₂. Murnaghan's logarithmic equation is then used to determine the compression curves of these solids. The agreement between the calculated and experimental compression-ratio values for these halides of cesium is good.     

Analytical application of embelin

Summary Embelin is employed as a reagent for the gravimetric individual estimation of alkaline earth metals and magnesium.

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Zusammenfassung Zur gravimetrischen Einzelbestimmung von Magnesium und den Erdalkalien wird Embelin als Reagens empfohlen.

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Part III: Z. analyt. Chem. 185, 216 (1962).     

干涉型光纤法布里-珀罗传感系统抗噪方法的实验研究

对于干涉型光纤法布里-珀罗(FFP)传感系统,外界环境对解调干涉仪的扰动是其主要噪声源之一.在光纤布拉格光栅构成的FFP传感系统中,对比分析了采用参考传感器和参考光源两种抗噪方法.实验结果表明,对于单频和宽带干扰,两种方法均可提高信噪比到40 dB.而且由于采用窄线宽光纤激光器作为参考光源的噪声水平较低,其差分探测结果具有更好的抗噪效果.     

Titrimetric determination of arsenic(III) with potassium dichromate, using redox indicators

Experimental conditions have been established for the accurate direct titrimetric determination of arsenic(III) with potassium dichromate, using ferroin and N-pnenylanthranilic acid as redox indicators. Interferences have been considered.     

Successive complexometric determination of thorium and uranium in sulphuric acid media

A selective analytical extraction method for rapid successive complexometric determination of thorium(IV) and uranium(VI) in sulphuric acid media is described. The method is based on the extraction of thorium and uranium from sulphuric acid media with N-butylaniline or N-benzylaniline in chloroform. Both thorium and uranium are selectively and quantitatively extracted in the presence of ascorbic acid and EDTA. Most cations and anions do not interfere. The reduction of uranium(VI) with sodium dithionite at room temperature is rapid and quantitative and superior to that with ascorbic acid, which reduces uranium(VI) in boiling solution. The method is simple, rapid and accurate, and the experimental conditions are not highly critical.     

Oxidimetric determination of sulphides

Hypoiodite oxidises sulphides much more rapidly than does iodate under comparable experimental conditions. A procedure is reported for the determination of soluble and insoluble sulphides by oxidation to sulphate with hypoiodite. This is an improvement over Bethge's iodate method.     

Comparison of standards in the Karl Fischer method for water determination.

The use of 4-(5-nonyl)pyridine oxide and trioctylamine oxide for the extraction of niobium(V) from different mineral acid solutions is described. The influence of the concentration of the solvents, acids and salting-out agents is discussed. Separations of niobium(V) from tantalum(V) and zirconium(IV) have been achieved.     

Peptides of azascrine

The synthesis of the cis and trans forms of the cyclic dipeptide of O-diazoacetyl-DL-serine is described.     

Photoelectron spectra of substituted benzenes

Photoelectron spectra of several substituted dimethylanilines, nitrobenzenes, acetophenones and nitrosobenzenes have been studied with a view to examine the electronic effects of substituents on the various φ and n levels. The results are discussed in the light of molecular orbital calculations and electronic absorption spectra. Correlation of substituent effects on the IE's with π-electron densities and Hammett substituent constants has enabled rationalization of all available data on mono- and disubstituted benzenes. The IE's generally increase with the electron-withdrawing power of the substituents.     

Thermal decomposition of titanyl oxalates IV. Strontium and calcium titanyl oxalates

Thermal decomposition of strontium titanyl oxalate tetrahydrate and calcium titanyl oxalate hexahydrate have been studied employing TG, DTA, gas and chemical analysis. The decompositions proceed through three major steps: dehydration, decomposition of the oxalate to a carbonate and the decomposition of the carbonate to yield the final products, the metatitanates. The intermediates of the oxalate decomposition are found to be Sr₂Ti₂O_4+x(CO₃)₂-x(CO₂)_x and Ca₂Ti₂O₄(CO₃)₂, respectively. The entrapment of carbon dioxide in the former and the presence of non-equivalent carbonate groups in the latter are substantiated by their i.r. spectra. The penultimate solid residues are poorly crystalline Sr₂Ti₂O₅CO₃ and amorphous Ca₂Ti₂O₅CO₃. Decompositions of these carbonates are accompanied by growth in particle size of the products, SrTiO₃ and CaTiO₃, respectively.