Møller was right

Direct calculation proves that the total energy-momentum vector derived from the Møller energy-momentum complex from 1958 does not transform like a free 4-vector with respect to the Lorentz transformation. This conforms with the conclusion formulated by Møller himself, but it contradicts the result of the critical analysis of Kovacs. Defects in Kovacs argumentation are found.     

Symmetry of electronic states in garnets

The paper presents the classification of the electronic empty lattice eigenvalues and the classification of the Bloch sums for the garnet structureIa3d (O _h ¹⁰ ) at the symmetry points, H, P, andN of the Brillouin zone. This provides a starting point for the energy band studies of these technologically important materials.The author thanks Dr. V. Frei for useful comments.     

Complex supersymmetry and supersymmetric skyrmion

Starting from the complex supersymmetry and showing that the stabilizing term is directly present in the kinetic term of the vector superfield, we show a possibility to obtain supersymmetric skyrmion.     

160Tb nuclear orientation in yttrium single crystal

First experimental results of¹⁶⁰Tb nuclear orientation in yttrium single crystal matrix are described. The influence of external magnetic field in combination with the crystal field interaction is discussed.     

Hyperfine anomalies and nuclear γ-factors of56Co,57Co and60Co isotopes studied by NMR/ON

The results of NMR/ON measurements on^56,57,60Co isotopes in iron are presented in the paper. To avoid the uncertainties caused by local demagnetizing field inhomogeneities the measurements on two cobalt isotopes in one sample have been carried out. The values of nuclear-factors ratios ⁵⁷/ ⁶⁰=1·805(20), ⁶⁰/ ⁵⁶ = 0·761(20), ⁵⁶/ ⁵⁷ = 0·726(20) and hyperfme anomalies^{56 60} = –0·036(10),^{60 57} = 0·017(10) and^{57 56} = 0·018(10) have been calculated from the experimental results.Dedicated to the 30th anniversary of the Joint Institute for Nuclear Research.     

Cinnamaldehyde hydrogenation using ruthenium-tin catalyst type

Bimetallic ruthenium-tin catalysts were prepared using the sol-gel method and the method of carrier impregnation. Two different procedures were used for their reduction — reduction in hydrogen atmosphere under an increased temperature, and reduction using an aqueous solution of sodium borohydride. Hydrogenation of 3-phenylpropenal (cinnamaldehyde) in tetrahydrofuran at 433 K and the total pressure 7 MPa was used as the model reaction for comparing the catalytic properties of the prepared catalysts. It was demonstrated that a tin addition notably affected catalytic properties of ruthenium in the sense of a selectivity increment related to the production of an unsaturated alcohol.     

Development of piezoelectric immunosensors for measurement of albuminuria

The development of piezoelectric immunosensors for human serum albumin (HSA) is reported. The piezoelectric crystals were modified either with monoclonal antibody AL-01 (direct assay) or with HSA (competitive assay). Measurements were carried out in the flow-through mode. Affinity interaction between albumin and the antibody was characterised. With immobilised antibody and HSA in solution, the kinetic association rate constant k(a) was 18 100 l mol(-1) s(-1) and the dissociation constant k(d) was 0.00369 s(-1). For the opposite arrangement (immobilised HSA), a slower dissociation was observed, k(d) was 0.00085 s(-1). A competitive assay for HSA was developed with working range of 1-5 mug ml(-1) and a total time for one analysis equal to 17 min. Samples of urine were analysed after tenfold dilution. The developed system was successfully evaluated on real samples from diabetic patients and the obtained results correlated well with the standard reflectometric assay of proteins in urine.     

Extraction of microamounts of calcium in the two-phase water-HCl-18-crown-6-nitrobenzene-hydrogen dicarbollylcobaltate system

Summary Extraction of microamounts of calcium by a nitrobenzene solution of hydrogen dicarbollylcobaltate (H⁺B^-) in the presence of 18-crown-6 (18C6, L) has been investigated. The equilibrium data have been explained assuming that the complexes HL⁺, CaL²⁺and CaL are extracted into the organic phase. The values of extraction and stability constants of the complex species in nitrobenzene saturated with water have been determined.