Some properties of milled vanadium phosphates

Mechanochemical modification of vanadium phosphates doped with Bi, Zr, Mo has been studied. Milled samples have been investigated by means of XRD, DTA-TG, FTIR, nitrogen adsorption, electrokinetic measurements. It was found that phase composition of the phosphates does not change upon the mechanochemical modification process. Milling in water causes formation of porous materials. Modification of surface results in changes of the electrokinetic and adsorption properties of the milled samples.     

Synthesis and spectral-luminescence properties of 2-(2′-tosylaminophenyl)benzimidazole and its substituted derivatives

Tosylamino-substituted 2-arylbenzimidazoles have blue or green fluorescence in the crystalline state and in toluene at room temperature. The effect of the substituents on the position of the absorption and fluorescence bands and on the strength of the intramolecular hydrogen bond was investigated. An anomalously large Stokesian shift within the limits 8800–11450 cm^¡1 is characteristic for compounds that contain an o-tosylamino group.     

Study of phase equilibria established up to the solidus line in the system Fe2V4O13−WO3

The phase equilibria established up to the solidus line in the system Fe₂V₄O₁₃−WO₃, one of the intersections of the three-component system Fe₂O₃−V₂O₅−WO₃, have been studied. The system appears not to be a real two-component system.

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Zusammenfassung Es wurde eine Untersuchung des Phasengleichgewichtes durchgeführt, welches bezüglich der Solidus-Linie im System Fe₂V₄O₁₃−WO₃, einer der Zwischenbereiche im Dreikomponentensystem Fe₂O₃−V₂O₅−WO₃, nachgewiesen wurde. Dieses System scheint kein echtes Zweikomponentensystem zu sein.

     

Speciation of chromium in mineral waters and salinas by solid-phase extraction and graphite furnace atomic absorption spectrometry

A simple GF-AAS method for speciation analysis of chromium in mineral waters and salinas was developed. Cr(VI) species were separated from Cr(III) by solid-phase extraction with APDC (ammonium pyrrolidinedithiocarbamate). The APDC complexes were formed in the sample solution under proper conditions, adsorbed on Diaion HP-2MG resin and the resin was separated from the sample. After elution with concentrated nitric acid Cr(VI) was determined by GF-AAS. Total chromium was determined by GF-AAS directly in the sample and Cr(III) concentration was calculated as the difference between those results.

The detection limit of the method defined as 3 s of background variation was 0.03 μg l⁻¹ for Cr(VI) and 0.3 μg l⁻¹ for total chromium. RSD for Cr(VI) determination at the concentration of 0.14 μg l⁻¹ was 9%, and for total chromium at the concentration of 5.6 μg l⁻¹ was 5%. The recovery of Cr(VI) was in the range of 94–100%, dependently on type of the sample.

The investigation of recovery of the spiked Cr(VI) showed that at concentration levels near 1 μg l⁻¹ and lower recovery may be reduced significantly even by pure reagents that seem to be free from any reductants.     

Collisional energy transfer in the two-channel decomposition of 1,1,2,2-tetrafluorocyclobutane and 1-methyl-2,2,3,3-tetrafluorocyclobutane, I. Gas/gas collisons

The two-channel thermal decomposition of 1,1,2,2-tetrafluorocyclobutane (TFCB) and 1-methyl-2,2,3,3-tetrafluorocyclobutane (MTFCB) have been studied in the temperature range of 730–805 K at pressures varied from 1.1 Pa up to 4.6 kPa. In the pressure independent range, Arrhenius expressions were obtained for TFCB decomposition into 2 CH₂CF₂ (k₁) and C₂H₄+C₂F₄ (k₂), respectively. The same kinetic equations were determined for the decomposition of MTFCB into C₃H₄F₂+C₂H₂F₂ (k₃) and C₃H₆+C₂F₄(k₄). From the study of the pressure dependence of the homogeneous decomposition rates, the average downward energy transfer values of 1800±200 cm^–1 and 1600±200 cm^–1 were obtained for the TFCB and MTFCB molecules, respectively.     

Configuration of 2-(4-pyridyl)-5-aryloxazole molecules in various states of aggregation

The electronic absorption and emission spectra in the crystals, solutions, vapor, and ethanol-ether (77 °K) were investigated for the series of 2-(4-pyridyl)-5-aryl-substituted oxazoles at various temperatures. The conjugation between the rings of the system was investigated by mass spectrometry. The combination of spectral data shows that the configurations of such molecules both in the ground state and in the excited state depends substantially on the state of aggregation and on the temperature.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 407–412, March, 1986.     

Phase equilibria up to the solidus line in the V2O5−Cr2(MoO4)3 system

Phase equilibria being established in the subsolidus area of the V₂O₅?Cr₂(MoO₄)₃ system at the whole component concentration range have been studied basing on DTA and X-ray phase powder diffraction. It has been established that the system is not a real two-component system in the subsolidus area. The fact has been proved by the presence of fields in that area, where three solid phases remain in mutual equilibrium.     

Carbon-mineral adsorbents prepared by pyrolysis of waste materials in the presence of tetrachloromethane

Natural bentonite spent in the process of plant oil bleaching was used as an initial material for preparation of carbon-mineral adsorbents. The spent bleaching earth was treated using four procedures: T (thermal treatment); H (hydrothermal treatment); C (thermal treatment with addition of CCl4 vapor); M (modification of porous structure). Raw bentonite, RB (raw bleaching earth), and carbon materials prepared using plant oil were compared. The physicochemical characteristics of the adsorbents were determined using different methods: nitrogen adsorption/desorption, XRD, TEM, and MS-TPD. Carbon-mineral adsorbents contain from 5.23 to 19.92% C (w/w) and carbon adsorbents include from 84.2 to 91.18% C (w/w). Parallel processes of organic substance carbonization, porous structure modification, sublimation or evaporation of metal chlorides, and removal of hydrogen chloride take place during pyrolysis of waste mineral materials in the CCl4 atmosphere.     

High-order mode based dispersion compensating modules using spatial mode conversion

High-Order Mode Dispersion Compensating Modules (HOM-DCM) using spatial optical transformations for mode conversion are reviewed. It is shown that mode transformers using this technology can be designed to transform the LP₀₁ mode of SMF fibers to the LP₀₂ mode of specially designed dispersion compensating High-Order Mode Fiber (HOMF), with typical insertion loss of ∼1 dB, and typical extinction ratio to other modes less than -20 dB. The HOMF itself can provide high negative dispersion [typically in the range of 400-600 ps/(nm km)], and high negative dispersion slope, allowing efficient compensation of all types of transmission fiber. Combining two mode transformers with HOMF and possibly trim fiber for fine-tuning, results, for example, in a HOM-DCM that compensates 100 km LEAF? fiber, with Insertion loss < 3.5 dB, and Multi-Path Interference (MPI) < -36 dB. MPI phenomena in HOM-DCMs is characterized, and shown to comprise both coherent and incoherent parts, and to result from both the mode transformers and fiber coupling within the HOMF. MPI values of < -36 dB have been shown to allow error free transmission of 10 Gb/s signals over up to 6000 km. Finally, a number of applications well suited to the properties of HOM-DCMs are reviewed.     

Synthesis and electrochemical study of nitrophenyl derivatives of β‐cyclodextrin

A series of nitrophenyl β‐cyclodextrin derivatives: mono[6‐deoxy‐6‐(4‐nitrobenzamido)]‐per‐ O‐methyl‐β‐cyclodextrin (R₁? Ph? NO₂), mono[6‐deoxy‐6‐(3‐nitrobenzamido)]‐per‐O‐methyl‐β‐cyclodextrin (R₂? Ph? NO₂) and heptakis[6‐deoxy‐6‐(4‐nitrobenzamido)‐2,3‐di‐O‐methyl]‐β‐cyclodextrin [R₃? (Ph? NO₂)₇] were synthesized. Purity and composition of the obtained substances were checked. Electroreduction of nitro groups of the new synthesized compounds was investigated on mercury electrode using cyclic voltammetry and chronocoulometry. The parameters of the reduction processes of ? NO₂ groups of the investigated compounds were found not to be comparable to the reduction of nitrobenzene under the same experimental conditions. Moreover, the electroreduction of nitro groups in these nitrophenyl derivatives was dependent on pH, the type of the studied compound, and slightly on the solvent composition. All the reactants were strongly adsorbed on mercury electrode. In the case of R₃? (Ph? NO₂)₇, its seven nitro groups were reduced practically at the same potential, and no radical anion formation was observed. Copyright © 2007 John Wiley & Sons, Ltd.