Disappearance of the heat capacity peak of Sc3In around the curie temperature in high magnetic fields

The low temperature (1.3–20.0 K) heat capacity of the weak itinerant electron ferromagnet Sc₃In was measured in magnetic fields up to ～ 10 T. The heat capacity peak observed around T_c = 6.0 K in zero field becomes smaller with increasing fields and at 9.98 T its magnetic entropy is ≈ 18% of the zero field value. Above T_c, the spin fluctuation contribution to the heat capacity, which is enhanced by the magnetic field at lower fields (?5 T), is quenched at higher fields (?5 T). This depression of the spin fluctuation contibution to the heat capacity by the high magnetic fields occurs at lower magnetic fields than had been considered possible heretofore. Our results suggest that the itinerant ferromagnetism is Sc₃In is completely quenched at 12 T.     

A case for large Auger recombination cross sections associated with deep centers in semiconductors

It is argued that the recent quantitative results concerning localized defects in semiconductors (e.g. GaAs) are consistent with the possibility of large Auger-type cross sections associated with recombination at these centers.It is proposed that many of the capture cross sections reported to be in the range 10^?13–10^?16cm², which exhibit only weak temperature dependence, and which do not depend on carrier concentration, might be explained by this mechanism.     

Hydrogen bonding effects on molecular structure: crystallographic studies of barbiturates

X-ray crystal structure determinations show systematic perturbations of the order of 0.01 Å in the oxopyrimidine rings of twelve barbiturate molecules. They appear to be related to the mode of intermolecular NHβO hydrogen bonding.     

Mixed ligand complexes of ruthenium(III), rhodium(III) and iridium(III) with dipicolinic acid and some monobasic bidentate nitrogen,oxygen donor ligands

The trivalent ruthenium, rhodium and iridium complexes of dipicolinic acid and its mixed ligand complexes with several nitrogen, oxygen donor molecules, of types: Na[M(dipic)₂]·2H₂O and [M(dipic)(N-O)]·nH₂O (where M = Ru(III), Rh(III) or Ir(III); dipicH₂ = dipicolinic acid; NOH represents different nitrogen, oxygen donor molecules, viz., picolinic acid, nicotinic acid, isonicotinic acid, glycine, aminophenol, o- or p-aminobenzoic acid), have been synthesized and characterised on the basis of elemental analyses, electrical conductance, magnetic susceptibility measurements and spectral (electronic and infrared) data. The parent dipicolinic acid complexes are found to have a six-coordinate pseudooctahedral structure, whereas for mixed ligand complexes, a polymeric six-coordinate structure has been assigned. Various ligand field and nephelauxetic parameters have also been evaluated.     

An automatic electrometer ranging circuit for a spark-source mass-spectrometer

An auto-ranging circuit which accommodates the erratic nature of the electrometer output signals from a spark-source mass-spectrometer is described briefly.     

The vibrational force field of halogenated aromatic molecules: II. Out-of-plane vibrations of fluoroaromatics

A general quadratic force field is determined for the out-of-plane vibrations of florobenzenes. The force constants for the out-of-plane wagging of both CH and CF bonds decrease by about 10 % for each ortho fluorine substituent. No significant meta dependence could be detected. It is shown that the present field is in excellent accord with the chlorobenzene field of Scherer and with the benzene fields of Whiffen and of Kydd when due allowance is made for differences in coordinate definitions.     

The anisotropic van der waals potential for He-N2

We have calculated the spherical v₀ and anisotropic radial components v₂ and v₄ in the usual Legendre expansion for the rigid rotor He-N₂ potential using the method of Tang and Toennies Potential curves covering the range of internuclear distances from 2.5 to 8.0 Å, which includes the minimum region, arc presented and compared with a recent experimental potential derived from differential total cross sections.     

A computer program system for kinetic analysis of non-isothermal thermogravimetric data: I. Data acquisition and preparation for kinetic analysis

FORTRAN software is described which enables the generation of rate of weight change data (DTG) from percentage weight change measurements (TG), obtained under non-isothermal conditions. The program also transposes this information into the dimensionless extent and rate of reaction at unit temperature intervals by means of a cubic spline interpolation. A simple search routine identifies all DTG spikes in the thermogravimetric record, and the temperature and extent of reaction at which the rate attains its maximum value. This total information serves as input data for the kinetic analysis software to be discussed in part II of this communication. An example of the application of this program to the pyrolysis of bituminous coal is presented.