Neutron reflection from a helical system

Analytical expressions for neutron reflection and transmission by magnetic mirrors with helical magnetization are derived. Reflectance curves with and without neutron spin flip are presented. Resonant properties of helical systems are studied.     

Spectroscopy of zinc-oxide cathode luminophores

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 54, No. 6, pp. 960–964, June, 1991.     

The reactivity of 3-methyl- and 5-methyl-1-vinylpyrazoles in free-radical polymerization

3-Methyl-l-vinylpyrazole (M3VP) and 5-methyl-1-vinylpyrazole (M5VP) were isolated as individual substances by vacuum rectification of their mixture (M3VP: M5VP 60 40). For each of them the kinetics of free-radical polymerization in MeOH were measured at low conversions. In both cases the rate of polymerization is proportional to 0.5 order with respect to the initiator (AIBN) concentration. On the other hand, a first order of reaction with respect to monomer concentration is observed only when the latter is relatively low (3M). At higher initial concentrations of monomers the order of reaction becomes less than unity. The overall rate of polymerization for M5VP was higher than for M3VP, whereas the initiation rate remained constant in the whole range of monomer concentrations and did not depend on the exact structure of the monomer. The difference in the rates of polymerization observed for M3VP and M5VP is probably connected with the difference in the key parameterk _p/k _t ^1/2 for each of the two isomers. It is concluded that the correct kinetic information about homo- and co-polymerization of M3VP and M5VP cannot be obtained without their adequate separation.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 413–415, February, 1993.     

Sulfide Catalysts Supported on Al2O3: VI. Synthesis of Catalysts with the Use of Binuclear Molybdenum(V) Complexes with Sulfur-Containing Ligands

A new method was developed for the preparation of sulfide catalysts supported on aluminum oxide. The surface assembling of a direct precursor of the active component was used in this method. The method consists in the sequential immobilization of binuclear molybdenum complexes with S-containing ligands on the support surface followed by the immobilization of nickel (cobalt) compounds at the surface molybdenum complexes. The complexation and structure of the resulting complexes in solution and the structure of surface complexes were studied by ⁹⁵Mo and ¹⁷O NMR, IR, and EXAFS spectroscopy. The surface assembling of a direct precursor of the active component of sulfide hydrodesulfurization catalysts was demonstrated using IR and EXAFS spectroscopy. The activity of the resulting catalysts in a model reaction of thiophene hydrogenolysis was comparable to the activity of sulfide catalysts of the metal complex origin and was much higher than the activity of commercial catalysts and catalysts prepared by impregnation.     

The synthesis and characterisation of ferromagnetic CaMn2O4 nanowires.

The synthesis of marokite CaMn(2)O(4) nanowires using a hydrothermal method is reported. Transmission electron microscopy and electron diffraction measurements show that the nanowires are polycrystalline in nature with diameters between 10 and 20 nm and lengths ranging from approximately 100 to 500 nm. Most interestingly, in contrast with the bulk material, magnetization measurements show that these nanowires exhibit ferromagnetic ordering with a Curie temperature (T(C)) of approximately 40 K.     

Sonochemical reactions with mesoporous alumina

Herein, we report the sonochemical reactions with MSU-X mesoporous alumina (m-Al₂O₃) in aqueous solutions. Sonication (f = 20 kHz, I = 30 W cm^?2, W_aq = 0.67 W mL^?1, T = 36–38 °C, Ar) causes significant acceleration of m-Al₂O₃ dissolution in the pH range of 4–11. Moreover, power ultrasound has a dramatic effect on the textural properties and phase composition of m-Al₂O₃. Short-time sonication at pH = 4 leads to the formation of nanorods and nanofibers of boehmite, AlO(OH). Prolonged ultrasonic treatment causes high aspect morphology transformation to aggregated nanosheets in weakly acid solutions or plated nanocrystals in alkaline solutions. Sonochemical products in alkaline medium are composed principally from boehmite and small amounts of bayerite, Al(OH)₃. Silent hydrolysis of m-Al₂O₃ yields boehmite at pH = 4 and bayerite at pH = 11. The effect of ultrasound on the textural properties of mesoporous alumina as well as on the transformation of nanosized bayerite to boehmite can be consistently attributed to the transient strong heating of the liquid shell surrounding the cavitation bubble which caused the chemical processes similar to those occurred during hydrothermal treatment.     

Nonreciprocal cell for neutrons

The effect of nonreciprocal transmission of thermal neutrons (λ = 3–6 Å) through a system of magnetic mirrors with a noncoplanar distribution of the magnetic induction is predicted and observed experimentally. The relative difference between the transmittances for the direct and inverse processes reaches 75%. Thereby, the feasibility of a nonreciprocal cell for spin-1/2 particles is demonstrated.