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Showing papers on "Antimony published in 1970"



Journal ArticleDOI
TL;DR: Antimony trisulphide was sintered on glass blanks and their electrical and photoconductive properties such as spectral distribution of photoconductivity, currentvoltage characteristics and lux-ampere relationship were presented.
Abstract: Antimony trisulphide was sintered on to glass blanks and their electrical and photoconductive properties such as spectral distribution of photoconductivity, current-voltage characteristics and lux-ampere relationship are presented.

70 citations




Journal ArticleDOI

50 citations


Journal ArticleDOI
TL;DR: In this article, the antimony trifluoride structure was refined to R 0·072 for 370 reflections, with a distorted octahedral co-ordination around an antimony atom.
Abstract: Crystals of antimony trifluoride are orthorhombic, space group C2cm, a= 4·95, b= 7·46, c= 7·26 A, as previously reported. The structure was refined by three-dimensional least-squares methods, to R 0·072 for 370 reflections. Each antimony atom has three close fluorine neighbours with mean Sb–F distances 1·92 A. These SbF3 units are then linked through three fluorine bridges (Sb⋯F 2·61 A) to form a three-dimensional network, with a much distorted octahedral co-ordination around the antimony atom.

43 citations



Journal ArticleDOI
TL;DR: In this article, the substitution of pentavalent arsenic, vanadium, chromium, manganese and antimony for phosphorus in apatites has been investigated, and the results show that vanadium and chromium completely replaced phosphorus in the calcium, strontium and barium fluor- and chlorapatites.

34 citations


Journal ArticleDOI
TL;DR: In this article, lattice strain induced by diffusion of phosphorus, arsenic, antimony and tin into silicon is studied through an X-ray double crystal spectrometer. And the results show that the amount of straining induced by impurity depends both on the size of impurity atoms diffused into silicon and on the impurity concentration.
Abstract: Lattice strains induced by diffusion of phosphorus, arsenic, antimony and tin into silicon are studied through an X-ray double crystal spectrometer. This quantitative experiment gives that the amount of lattice strain induced by diffusion of impurity depends both on the size of impurity atoms diffused into silicon and on the impurity concentration, which agrees with the equation by S. Prussin et al. It also leads to the result as follows; the lattice strain in the diffused layer is compensated in the case of the phosphorus content less than 4×1020 atoms/cm3 by diffusing both tin, whose atomic radius is larger than that of silicon, and phosphorus with smaller radius. Anomaly in the diffraction pattern is also observed in the case of anomalous diffusion of phosphorus under high vapor pressure of phosphorus.

34 citations


Journal ArticleDOI
TL;DR: In this paper, the authors used the laser mass spectrometer to study the vapor composition of various compounds of arsenic and antimony with the elements of Group VIa and showed that in some cases there is a direct correlation between vapor composition and the structure of the condensed phase.
Abstract: The laser mass spectrometer has been used to study the vapor composition of various compounds of arsenic and antimony with the elements of Group VIa. It is shown that in some cases there is a direct correlation between the vapor composition and the structure of the condensed phase. The mechanism of the laser‐induced vaporization is discussed; it is shown that the critical region (or vicinity) can be reached in laser–solid interactions.

30 citations


Journal ArticleDOI
TL;DR: Antimony (III) species in sulphuric acid solutions have been investigated by u.v. spectrophotometry, ion exchange, solvent extraction and polarography as mentioned in this paper.

Journal ArticleDOI
TL;DR: By bombarding samples with 1.1•MeV 4He+ ions and observing the energy spectra of the backscattered ions, it has been possible to determine the concentrations and lattice locations of arsenic and antimony impurities diffused into silicon as mentioned in this paper.
Abstract: By bombarding samples with 1.1‐MeV 4He+ ions and observing the energy spectra of the backscattered ions, it has been possible to determine the concentrations and lattice locations of arsenic and antimony impurities diffused into silicon. For the samples investigated it was found that only 60–75% of the arsenic atoms were in substitutional sites, even at impurity concentrations well below solid solubility. About 90% of the antimony atoms were found to be in substitutional sites.


Journal ArticleDOI
Kamran Aykan1, Arthur W. Sleight1
TL;DR: In this article, the system U-Sb-O was examined in air up to 1000°C for ternary compounds and the products were characterized by chemical analysis, density determinations, TGA, X-ray diffraction techniques, and magnetic measurements.
Abstract: The system U-Sb-O was examined in air up to 1000°C for ternary compounds. The products were characterized by chemical analysis, density determinations, TGA, X-ray diffraction techniques, and magnetic measurements. The ternary compounds found were USbO5 and USb3O10. All cations are pentavalent in these new compounds, which are crystallographically related to α-UO3 and U3O8.

Journal ArticleDOI
TL;DR: In this article, a phase diagram for the yttrium-antimony system based on thermal, microscopic, chemical and X-ray analyses is proposed, which shows that an inverted peritectic reaction develops as a result of antimony additions, lowering the 1475° C transformation temperature of YSb to 1462° C.
Abstract: A phase diagram is proposed for the yttrium-antimony system based on thermal, microscopic, chemical and X-ray analyses. An inverted peritectic reaction develops as a result of antimony additions, lowering the 1475° C transformation temperature of yttrium to 1462° C. Eutectic reactions occur at 14.5 at. % antimony and 1220° C, and greater than 99.0 at.% antimony and 629° C. There are four compounds in the system. The compound YSb melts congruently at 2310° C while Y 3 Sb and Y 5 Sb 3 result from peritectic reactions at 1240° and 1690° C. The fourth compound, Y 4 Sb 3 , forms peritectically at 2120° C, but decomposes by a eutectoid reaction at 1660° C.

Journal ArticleDOI
TL;DR: In this article, the low energy properties of the odd mass Sb isotopes from A = 115 to A = 125 have been calculated in a semi-microscopic model.

Journal ArticleDOI
TL;DR: The formation of the complexes of trivalent antimony ion with the following ligands has been investigated with pH measurements as mentioned in this paper, and a classification of the ligands with respect to their ability to sequester the cation studied is given.
Abstract: The formation of the complexes of trivalent antimony ion with the following ligands has been investigated with pH measurements: D-tartaric acid, L-tartaric acid, catechol, catechol-3,5-disulfonic acid, 2,3-dihydroxybenzoic acid, mercaptoacetic acid, rac-thiomalic acid, meso-, rac-dithiotartaric acid, and mercapto-ethanol. Using the determined equilibrium constants, a classification of the ligands with respect to their ability to sequester the cation studied is given. In a discussion in which data of the literature are also included the structure of the tartar emetic, the possibility of a volumetric determination of the antimony, some problems concerning the coordination number, and the structure of the complexes are examined.


Journal ArticleDOI
TL;DR: In this article, the infrared spectra of SbF5 and AsF5 suspended in argon and neon matrices have been recorded between 4000 and 100 cm−1.
Abstract: The infrared spectra of SbF5 and AsF5 suspended in argon and neon matrices have been recorded between 4000 and 100 cm−1. The spectra of SbF5 and AsF5 are radically different and show that monomeric SbF5 belongs to symmetry group C4υ rather than to group D3h. The spectral effects induced by forming solid SbF5 from the monomers are understood in terms of associations through Sb–F–Sb fluorine bridge bonds. The behavior is compared with that observed previously for SF4. No evidence for fluorine bridging occurs with AsF5.


Journal ArticleDOI
TL;DR: In this article, the gas-phase laser Raman spectra of phosphorus and arsenic mixed vapours and phosphorus and antimony mixed mixture were investigated as a function of composition and temperature up to 1000 °C.
Abstract: The gas-phase laser Raman spectra of phosphorus and arsenic mixed vapours and phosphorus and antimony mixed vapours are investigated as a function of composition and temperature up to 1000 °C. The data are consistent with the presence of the tetratomic molecules PnAs4–n where n= 0–4. Under our experimental conditions SbP3 is probably the main (mixed) constituent in phosphorus–antimony mixed vapours. The polarization and relative intensity data together with the computed frequencies for As3P, AsP3, and SbP3 proved useful in the assignment of bands to the different molecular species.

Journal ArticleDOI
TL;DR: In this article, the concentration profiles of 20-keV high-temperature ion-implanted antimony into a silicon single crystal were measured by means of radioactivation analysis and the enhanced diffusion was observed.
Abstract: Concentration profiles of 20‐keV high‐temperature ion‐implanted antimony into a silicon single crystal were measured by means of radioactivation analysis and the enhanced diffusion was observed. The concentration profiles were found to be independent of temperature over the range between 500 °C and 800 °C and to be dependent on the dose rate of ion implantation. The diffusion coefficient of antimony is estimated to be about 1.1×10−15 cm2/sec for the dose rate of about 1.2×1012 ions/cm2 sec and about 6.6×10−15 cm2/sec for that of about 7.2×1012 ions/cm2 sec. The measured concentration profiles are in good agreement with the calculated concentration profile. These results are explained on the basis of a vacancy mechanism.




Journal ArticleDOI
TL;DR: In this article, strong base is added to solutions containing complexes of trivalent antimony with aminopolycarboxylates, these ligands are displaced, and oversaturated solutions of antimony (III) hydroxide are formed.
Abstract: If a strong base is added to solutions containing complexes of trivalent antimony with aminopolycarboxylates, these ligands are displaced, and oversaturated solutions of antimony (III) hydroxide are formed. This reaction has been used to investigate the formation of complexes of SbIII with the following ligands: N′-hydroxyethyl-ethylenediamine-N,N,N′-triacetate ion, ethylenediamine-N,N,N′,N′-tetraacetate ion, 1,2-diaminocyclohexane-N,N,N′,N′-tetraacetate ion, and diethylenetriamine-N,N,N′,N″,N″-pentaacetate ion.

Journal ArticleDOI
TL;DR: In this paper, no evidence could be found to support the existence of Sb2S5.121 Sb Mossbauer spectroscopy has been used to study some antimony chalcogenides.
Abstract: 121 Sb Mossbauer spectroscopy has been used to study some antimony chalcogenides: no evidence could be found to support the existence of Sb2S5.

Journal ArticleDOI
TL;DR: In this paper, the internal fields at the palladium, manganese, tin and antimony nuclei in the alloys Pd 2 MnSn and Pd2 MnSb were measured by spin-echo technique.

Patent
Paul C Yates1
30 Nov 1970
TL;DR: In this paper, the authors present a set of solutions of PENTAVALENT ANTIMONY-ALPHA-HYDROXY CARBOXYLIX ACID COMPOUNDS.
Abstract: SOLUTIONS OF PENTAVALENT ANTIMONY-ALPHA-HYDROXY CARBOXYLIX ACID COMPOUNDS OR OF HYDROUS PENTAVALENT ANTIMONY SOLS STABILIZED WITH AN ALPH-HYDROXY CARBOXYLIC ACID IN POLAR ORGANIC SOLVENTS SUITABLE FOR SPINNING OR CASTING ORGANIC POLYMERS ARE USEFUL FOR DISPERSING FLAME-RETARDING PENTAVALENT ANTIMONY COMPOUNDS IN POLYMERIC STRUCTURES.

Patent
15 Jun 1970
TL;DR: In this article, a metathesis reaction in an inert organic solvent between lithium tetrafluoroborate and an alkali metal compound of the formula ZMF6, wherein Z is potassium or sodium and M is as defined above, is described.
Abstract: Lithium compounds of the formula LiMF6 wherein M is arsenic or antimony are prepared by a metathesis reaction in an inert organic solvent between lithium tetrafluoroborate and an alkali metal compound of the formula ZMF6, wherein Z is potassium or sodium and M is as defined above.