First-principle study of antimony doping effects on the iron-based superconductor CaFe(Sbx_{x}As1−x_{1-x})2_{2}

We study antimony doping effects in the iron-based superconductor CaFe(Sb$_{x}$As$_{1-x}$)$_{2}$ by using the first-principle calculation. The calculations reveal that the substitution of the doped antimony atom into As of the chainlike As layers is more stable than that in FeAs layers. This prediction can be checked by experiments. Our results suggest that doping homologous elements into the chainlike As layers existing only in novel 112 system is responsible for rising up the critical temperature. We discuss antimony doping effects on the electronic structure. It is found that the calculated band structures with and without the antimony doping are similar to each other within our framework.Comment: 5 pages, 5 figures, 2 table

Thermogravimetric and distillation studies on mercury, antimony and arsenic sulfides

Thermogravimetric studies were made on naturally occurring sulfides of mercury, antimony and arsenic to determine activation energies and Arrhenius rates of reaction in vacuum and in atmospheres of air and nitrogen. Of the three sulfides only antimony showed an appreciable change in rate of reaction for the different test conditions. Distillation results on three flotation concentrates from Alaska mining operations showed that cinnabar (mercury sulfide) could be distilled in a closed system, with over 99 percent recovery of the mercury as metal when the sulfur was reacted with iron. Over 98 percent mercury recovery was obtained from a cinnabar-stibnite (antimony sulfide) concentrate, with less than 1 percent of the antimony distilled from the furnace charge. Cinnabarrealgar-orpiment (arsenic sulfides) could not be separated by distillation and large quantities of soot (condenser residue) formed with the metallic mercury in the condenser

Use of radiation in preparative chemistry

A summary and updating of previous work on the use of radiation chemistry for the preparation of pure materials are presented. Work was chiefly concerned with the reduction of metal salts in solution to the free metal using 2 MeV electrons. Metals deposited from aqueous solution are copper, silver, zinc, cadmium, thallium, tin, lead, antimony, iron, nickel, cobalt, and palladium. Dry organic solvents were evaluated for the deposition of metals based on a study involving deposition of antimony from soltions of antimony (III) chloride. The use of organic liquids for the preparation of anhydrous metal halides is also presented. Reaction mechanisms for both organic liquids and aqueous system are discussed

A speculum of chymical practice: Isaac Newton, Martin Lister (1639 −1712), and the making of telescopic mirrors

In 1674 the natural philosopher and physician Martin Lister published a new method of making glass of antimony for telescopic mirrors, using Derbyshire cawk or barite as a flux. New manuscript evidence reveals that Sir Isaac Newton requested samples of the cawk and antimony from Lister through an intermediary named Nathaniel Johnston. An analysis of Lister’s paper and Johnston’s correspondence and its context reveals insights not only about Newton’s work with telescopic specula but also about his alchemical investigations. Analysing these sources also contributes to our understanding of the nature of correspondence networks in the early ‘scientific revolution’ in England

Effect of Antimony and Cerium on the Formation of Chunky Graphite during Solidification of Heavy-Section Castings of Near-Eutectic Spheroidal Graphite Irons

Thermal analysis is applied to the study of the formation of chunky graphite (CHG) in heavysection castings of spheroidal graphite cast irons. To that aim, near-eutectic melts prepared in one single cast house were poured into molds containing up to four large cubic blocks 30 cm in size. Four melts have been prepared and cast that had a cerium content varying in relation with the spheroidizing alloy used. Postinoculation or addition of antimony was achieved by fixing appropriate amounts of materials in the gating system of each block. Cooling curves recorded in the center of the blocks show that solidification proceeds in three steps: a short primary deposition of graphite followed by an initial and then a bulk eutectic reaction. Formation of CHG could be unambiguously associated with increased recalescence during the bulk eutectic reaction. While antimony strongly decreases the amount of CHG, it appears that the ratio of the contents in antimony and cerium should be higher than 0.8 in order to avoid this graphite degeneracy

Stratabound arsenic and vein antimony mineralisation in Silurian greywackes at Glendinning, south Scotland

Stratiform and disseminated pyrite-arsenopyrite concentrations are overprinted by fracturecontrolled polymetallic mineralisation including stibnite through at least tens of metres of Silurian sediments at Glendinning, near Langholm. Three shallow boreholes were drilled on an anomaly defined by VLF-EM and II? surveys and by antimony values X0 ppm in thin B-C horizon soils. A parallel conductive zone with an accompanying soil anomaly but lacking an IP response was investigated by a fourth hole. The stratabound sulphides form disseminations and bands parallel to the bedding and are particularly concentrated in intraformational breccia units regarded as debris flows, which, together with the presence of smaIl scale slump folds in the greywackes, testify to the existence of an unstable slope during sedimentation. The thickest such unit has a true thickness of 4 m and together with 8 m of adjoining greywackes grades 0.7% As. Phases of fracture-controlled Fe-As-Sb-Pb- Zn-Cu-(?)Hg mineralisation associated with widespread dolomite and quartz veinlets and narrow breccia veins are superimposed on the stratabound mineralisation. Their spatial association with the stratabound mineralisation, the presence of up to 0.33% Sb in the stratiform arsenopyrite and as much as 5% As in the stratiform pyrite, favour a common source for the arsenic and antimony. This source was probably a synsedimentary metal accumulation in a mid or lower fan environment where euxinic conditions periodically developed

The co-pyrolysis of flame retarded high impact polystyrene and polyolefins

The co-pyrolysis of brominated high impact polystyrene (Br-HIPS) with polyolefins using a fixed bed reactor has been investigated, in particular, the effect that different types brominated aryl compounds and antimony trioxide have on the pyrolysis products. The pyrolysis products were analysed using FT-IR, GC-FID, GC-MS, and GC-ECD. Liquid chromatography was used to separate the oils/waxes so that a more detailed analysis of the aliphatic, aromatic, and polar fractions could be carried out. It was found that interaction occurs between Br-HIPS and polyolefins during co-pyrolysis and that the presence of antimony trioxide influences the pyrolysis mass balance. Analysis of the Br-HIPS + polyolefin co-pyrolysis products showed that the presence of polyolefins led to an increase in the concentration of alkyl and vinyl mono-substituted benzene rings in the pyrolysis oil/wax resulting from Br-HIPS pyrolysis. The presence of Br-HIPS also had an impact on the oil/wax products of polyolefin pyrolysis, particularly on the polyethylene oil/wax composition which converted from being a mixture of 1-alkenes and n-alkanes to mostly n-alkanes. Antimony trioxide had very little impact on the polyolefin wax/oil composition but it did suppress the formation of styrene and alpha-methyl styrene and increase the formation of ethylbenzene and cumene during the pyrolysis of the Br-HIPS

Energy Conversion Using New Thermoelectric Generator

During recent years, microelectronics helped to develop complex and varied technologies. It appears that many of these technologies can be applied successfully to realize Seebeck micro generators: photolithography and deposition methods allow to elaborate thin thermoelectric structures at the micro-scale level. Our goal is to scavenge energy by developing a miniature power source for operating electronic components. First Bi and Sb micro-devices on silicon glass substrate have been manufactured with an area of 1cm2 including more than one hundred junctions. Each step of process fabrication has been optimized: photolithography, deposition process, anneals conditions and metallic connections. Different device structures have been realized with different micro-line dimensions. Each devices performance will be reviewed and discussed in function of their design structure.Comment: Submitted on behalf of TIMA Editions (http://irevues.inist.fr/tima-editions