Abscheidung von Glimmpolymerschichten in einem weiten Metallrezipienten und Untersuchungen zur Struktur

Investigations are reported of growth rate, chemical structure (IR-spectroscopy, mass-spectrometry), thermal stability, surface structure (scanning electron microscopy) of thin polymeric films grown in a gas (Ar-hexamethyldisiloxane-mixture) discharge with a heated cathode, which is situated in the centre of a cylindrical metallic vessel (l = 50 cm, 2r = 30 cm). The discharge conditions are the following: I = 0,25 – 4 A, U = 30 – 100 V, p = 6 – 40 Pa, argon flow rate = 3,8 · 10^?5 mol/min, Ar/HMDS = 1 : 0,7 – 1 : 2,4. The growth rate changes from 2 to 18 nm/min, depending on the discharge conditions. The reproducibility of the growth rate shows deviations smaller than 10%. The films consist of a highly cross linked polymeric material and are stable up to 260°C, the solubility in n-hexane being smaller than 2%. The surface of the thin film (d ～ 10² nm) is smooth. Corrosion resistance to soda lye (0,2% NaOH) has been proved.     

Determination of Busulfan in Tablets by NMR Spectroscopy

A simple NMR spectroscopic method is described for the assay of busulfan in tablets. Methenamine is used as the internal standard and chloroform-d as the solvent. The mean recovery value for the drug from standard mixtures was 99.3 ± 0.182% w/w (n = 5) by the NMR method and 99.2% (n = 2) by the official method. The mean content of busulfan in commercial tablet samples was 99.4 ± 0.16 (range 99.1 – 99.6)% w/w (CV = 0.16%, n = 10) by the NMR method and 99.5 ± 0.17 (range 99.2 – 99.8)% w/w (CV = 0.17%, n = 10) by the official method.     

Получение изотопа С13 методом ректиФикации окиси углерода

A prompt activation technique – detection of the α-particles with surface barrier silicon and solid state track detectors, detection of the γ rays with (GeLi) detector – based on the ¹⁰B(n, α)⁷Li nuclear reaction was applied for boron determination using a time-of-flight technique on the IBR-30 pulsing reactor. The method was used for measurement of the boron concentration and distribution in bean and maize leaves.     

Thermal characterisation of dye-intercalated K-10 montmorillonite ceramics using photoacoustic technique

Thermal diffusivity (TD) measurements were performed on some industrially important dyes – auramine O (AO), malachite green and methylene blue (MB) – adsorbed K-10 montmorillonites using photoacoustic method. The TD value for the dye-adsorbed clay mineral was observed to change with a variation in dye concentration. The contribution of the dye towards TD was also determined. The repeatedly adsorbed samples with MB and AO exhibited a lower TD than the single-adsorbed samples. TD values of sintered MB samples were also obtained experimentally. These sintered samples exhibit a higher TD, although they show a trend similar to that of non-sintered pellets. A variation in dye concentration and sintering temperature can be used for tuning the TD value of the clay mineral to the desired level.     

A Study on Spectro-Analytical Aspects,DNA – Interaction,Photo-Cleavage,Radical Scavenging,Cytotoxic Activities,Antibacterial and Docking Properties of 3 – (1 – (6 – methoxybenzo [d] thiazol – 2 – ylimino) ethyl) – 6 – methyl – 3H – pyran - 2, 4 – dione and its Metal Complexes

The focus of the present work is on the design, synthesis, characterization, DNA-interaction, photo-cleavage, radical scavenging, in-vitro cytotoxicity, antimicrobial, docking and kinetic studies of Cu (II), Cd (II), Ce (IV) and Zr (IV) metal complexes of an imine derivative, 3 – (1 – (6 – methoxybenzo [d] thiazol – 2 – ylimino) ethyl) – 6 – methyl – 3H – pyran – 2, 4 – dione. The investigation of metal ligand interactions for the determination of composition of metal complexes, corresponding kinetic studies and antioxidant activity in solution was carried out by spectrophotometric methods. The synthesized metal complexes were characterized by EDX analysis, Mass, IR, ¹H-NMR, ¹³C-NMR and UV–Visible spectra. DNA binding studies of metal complexes with Calf thymus (CT) DNA were carried out at room temperature by employing UV-Vis electron absorption, fluorescence emission and viscosity measurement techniques. The results revealed that these complexes interact with DNA through intercalation. The results of in vitro antibacterial studies showed the enhanced activity of chelating agent in metal chelated form and thus inferring scope for further development of new therapeutic drugs. Cell viability experiments indicated that all complexes showed significant dose dependent cytotoxicity in selected cell lines. The molecular modeling and docking studies were carried out with energy minimized structures of metal complexes to identify the receptor to metal interactions.     

Investigation of regeneration effect of blue luminescence in NaCl using variable delay optically stimulated luminescence (VD-OSL)

Optically stimulated luminescence (OSL) of pure analytical sodium chloride (NaCl) was studied. Performing series of CW-OSL (continuous wave OSL) readouts it was found that subsequent CW-OSL decay, after some delay, starts from significantly higher intensity level than the final intensity of the previous readout. To study this ‘regeneration effect’ a new type of measurements was implemented – the variable delay OSL (VD-OSL) method. The idea of VD-OSL is explained – it allows to study OSL kinetics at very long time scale. VD-OSL data confirm coexistence of two effects in NaCl – regeneration and fading of the OSL signal. After partial CW-OSL readout, regeneration predominates in the short time scale of the order of 10³ s. Then, fading becomes dominant. The same measurements were applied to commonly used Al₂O₃:C material as well. Nevertheless, the results do not show such behavior at the studied time scale. Theoretical arguments are presented that the regeneration mechanism cannot be explained on the basis of the simple trap model.     

The Arc Cathode Regime: An Approach from Basic Laws

The question is examined whether or not the existence of a cathode mechanism with high power density may be predicted from general physical laws, as well as the order of magnitude of the main cathode parameters of such a discharge. The answer is yes, though – because of many feedbacks and simplifications – the numerical values calculated in this way are not more than crude estimations. Essentially two conditions have to be fulfilled: The first is the dominance of collective electron emission processes, the second is the dominance of Joule heating combined with the limit of stationarity. Both conditions result in similar values of the cathode parameters. In this low-current region (about 10…100 A) the existence of a high-current density cathode mechanism (order of magnitude: 10⁸ A/cm²) is proved, with consequences for all the other parameters, in rough agreement with the results of measurements in arc cathode spots. Thus the typical arc spot regime may be founded theoretically by these argumentations.     

Electrochemical properties and radical anions of carbocycle‐fluorinated quinoxalines and their substituted derivatives

Electrochemical reduction (ECR) and oxidation (ECO) of 5,6,7,8‐tetrafluoroquinoxaline ( 1 ) and its derivatives bearing various substituents R (7‐H ( 2 ), 7,8‐H₂ (3 ), 6‐CF₃ ( 4 ), 6‐Cl ( 5 ), 5,7‐Cl₂ ( 6 ), 5‐NH₂ ( 7 ), 6‐OCH₃ ( 8 ), 6,7‐(OCH₃)₂ ( 9 ), 6,7,8‐(OCH₃)₃ ( 10 ), 5,6,7,8‐(OCH₃)₄ ( 11 ), 6‐OCH₃,7‐N(CH₃)₂ ( 12 ), 6‐N(CH₃)₂ ( 13 ), 6,7‐(N(CH₃)₂)₂ ( 14 ), 5,6,7‐(N(CH₃)₂)₃ ( 15 ), and 7,8‐cyclo‐(=CF‐CF = CF‐CF=) ( 16 )) in the carbocycle have been studied by cyclic voltammetry in MeCN. For 1 – 4 and 7 – 15 , the first reduction peaks have been found to be 1‐electron and reversible, thus corresponding to the formation of their radical anions (RAs), which are long lived at 295 K except those of 4 – 6 and 15 , 16 . Irreversible hydrodechlorination has been observed for 5 and 6 at the first step of their ECR confirmed by EPR detection of corresponding RAs of 2 and 5,7‐H₂ derivative of 1 ( 17 ) at the next steps. Electrochemically generated RAs of 1 – 3 , 7 – 14 , and 17 have been characterized in MeCN by EPR spectroscopy together with DFT calculations at the (U)B3LYP/6‐31 + G(d) level of theory using PCM to describe the solvent. A noticeable alternation of spin density on the –NCCN– moiety of quinoxaline has been observed for all RAs possessing R‐substitution asymmetry. The comparative electron‐accepting ability of 1 – 15 has been analyzed in terms of their experimental reduction peak potentials and the (U)B3LYP/6‐31 + G(d)‐calculated gas‐phase first adiabatic electron affinities (EAs). The differences in electron transfer solvation energies for 1 – 15 have been evaluated on the basis of ECR peaks' potentials and calculated gas‐phase EAs. The ECO of 1 – 5 and 7 – 14 has been found to be irreversible.     

On the binding energies and configurations of vacancy and copper–vacancy clusters in bcc Fe–Cu:a computational study

The properties of trapping centres in – as grown – Tl₄GaIn₃S₈ layered single crystals were investigated in the temperature range of 10–300 K using thermoluminescence (TL) measurements. TL curve was analysed to characterize the defects responsible for the observed peaks. Thermal activation energies of the trapping centres were determined using various methods: curve fitting, initial rise and peak shape methods. The results indicated that the peak observed in the low-temperature region composed of many overlapped peaks corresponding to distributed trapping centres in the crystal structure. The apparent thermal energies of the distributed traps were observed to be shifted from ~12 to ~125 meV by increasing the illumination temperature from 10 to 36 K. The analysis revealed that the first-order kinetics (slow retrapping) obeys for deeper level located at 292 meV.     

Simultaneous Determination of Ritodrine and Isoxsuprine Using Coupling Technique of Synchronous Fluorimetry and H-Point Standard Addition Method

Simultaneous determination of two structurally related ß₂ adrenergic receptor agonists namely, Ritodrine HCl (RTH) and Isoxsuprine HCl (ISP) was performed using coupling technique of synchronous fluorimetry and H-point standard addition method. Under optimum conditions, linear determination ranges were 1.48 – 14.80?×?10^?6 mol L^?1 and 1.54 – 15.44?×?10^?6 mol L^?1 for ISP and RTH respectively. RTH and ISP could be determined simultaneously without interference from each other when their concentration ratio varies from 5:1 to 1:5 in the mixed sample. The proposed method was applied to the determination of RTH and ISP in synthetic mixture of pharmaceutical samples, the accuracy and precision of the results were satisfactory.     

Experimental Determination of Ground and Excited State Dipole Moments of N,N-Bis (2, 5-di-tert-butylphenyl)-3, 4:9, 10-perylenebis (dicarboximide) (DBPI) A Photostable Laser Dye

In the present work, the absorption, emission spectra and dipole moments(μ_g, μ_e) of N, N-bis (2, 5-di-tert-butylphenyl)-3, 4:9, 10- perylenebis (dicarboximide) (DBPI) have been studied in solvents of various polarities at room temperature. Using the methods of solvatochromism, the difference between the first excited singlet state (μ_e) and ground state (μ_g) dipole moments was estimated from Lippert – Mataga,, Bakhshiev, Kawski – Chamma – Viallet equations. The change in dipole moment (Δμ) was also calculated using the variation of the Stokes shift with microscopic solvent polarity parameter (E _T ^N ). It was observed that the value of excited singlet state dipole moment is higher (3.53 Debye) than the ground state one (1.92Debye), showing that the excited state of DBPI is more polar than the ground state.     

高剥离态74W软X射线谱半连续带研究

在星光—Ⅱ激光装置上，用ＰＥＴ平晶谱仪观测了７４Ｗ高离化度激光等离子体软Ｘ射线发射谱，波长范围是０．３６～０．５２ｎｍ。准确测量和辨认了３ｄｊ－ｎｆｊ（ｎ＝５，６）４条类Ｎｉ共振线及附近类Ｃｕ、类Ｚｎ、类Ｇａ和类Ｇｅ几个电离级１６个半连续带结构谱。实验谱波长测量误差小于０．０００５ｎｍ，与用相对论自旋轨道劈裂跃迁组（ＳＯＳＡ）模型（不可分辨跃迁组（ＵＴＡ）特例）和Ｘα法理论计算结果符合很好。首次提迭加峰平均波长与离子离化度间关系式。     

Characterization of minerals in natural and manufactured sand in Cauvery River belt,Tamilnadu, India

The present study investigates the characterization of minerals in the River Sand (R – Sand) and the Manufactured sand (M-Sand) through FTIR spectroscopic studies. The R – Sand is collected from seven different locations in Cauvery River and M – Sand is collected from eight different manufactures around the Cauvery River belt in Salem, Erode, Tirupur and Namakkal districts of Tamilnadu, India. To extend the effectiveness of the analysis, the samples were subjected to grain size separation to classify the bulk samples into different grain sizes. All the samples were analyzed using FTIR spectrometer. The number of minerals identified with the help of FTIR spectra in overall (bulk) samples of R – Sand is 14 and of M – Sand is 13. The number has been increased while going for grain size separation, i.e., from 14 to 31 for R – Sand and from 13 to 20 for M – Sand. Among all minerals, quartz plays a major role. The relative distribution and the crystallinity nature of quartz have been discussed based on the extinction co-efficient and the crystallinity index values computed. There is no major variation found in M – Sand while going for grain size separation.     

The first second of the Universe

The history of the Universe after its first second is now tested by high quality observations of light element abundances and temperature anisotropies of the cosmic microwave background. The epoch of the first second itself has not been tested directly yet; however, it is constrained by experiments at particle and heavy ion accelerators. Here I attempt to describe the epoch between the electroweak transition and the primordial nucleosynthesis. The most dramatic event in that era is the quark‐hadron transition at 10 μs. Quarks and gluons condense to form a gas of nucleons and light mesons, the latter decay subsequently. At the end of the first second, neutrinos and neutrons decouple from the radiation fluid. The quark‐hadron transition and dissipative processes during the first second prepare the initial conditions for the synthesis of the first nuclei. As for the cold dark matter (CDM), WIMPs (weakly interacting massive particles) – the most popular candidates for the CDM – decouple from the presently known forms of matter, chemically (freeze‐out) at 10 ns and kinetically at 1 ms. The chemical decoupling fixes their present abundances and dissipative processes during and after thermal decoupling set the scale for the very first WIMP clouds.     

Electromagnetic absorption of SRR based double-inverse E-Shaped metamaterial for DCS,EESC, 5G,and WiMAX applications

Herein, a novel double-inverse E-structured resonator metamaterial (MTM) surrounded by split-ring resonators (SRRs) is introduced and proposed. The proposed MTM has working frequency ranges of 1.62 – 1.79 GHz, 2.08 – 2.21 GHz, 4.39 – 4.99 GHz, and 5.65 – 6.09 GHz. In addition, the proposed MTM can be applied in digital cellular system uplinks (DCS) (1.736 GHz), earth exploration-satellite communication (EESC) (2.148 GHz), lower band 5G (4.8 GHz), and WiMAX (5.89 GHz) applications. The electromagnetic radiation reduction performance of the proposed MTM is investigated at 900 MHz and 1800 MHz of GSM cellular bands. The Finite Integration Technique (FIT) based on high-frequency electromagnetic software is utilised for the development of design along with a detailed investigation of the MTM properties. The proposed MTM is formed by developing a double-inverse E-structure in the middle surrounded by SRRs. The resonator structure with SRRs is implemented on an epoxy resin FR4 substrate, which has a compact size of 11.11 × 11.11 mm². The unit cell has a high effective medium ratio of 14.82. Furthermore, the developed MTM shows a negative refractive index region from 3.124 to 6.98 GHz and double-negative region from 3.94 to 4.57 GHz, 5.26 to 5.49 GHz, and 6.29 to 6.88 GHz. In addition, SAR evaluation is also performed to test the competence of utilising the proposed MTM on modern mobile phones. The MTM has an electromagnetic absorption rate of about 44% and 43% at 900 MHz and 1800 MHz, respectively, for 1g whereas about 43% and 44% at 900 MHz and 1800 MHz, respectively, for 10g. Thus, the performance and characteristics of the developed MTM can be utilised for the above-mentioned applications.     

Light scattering by single magnons in FeF3

Scattering of laser light from single magnons has been observed in the canted antiferromagnet FeF₃ as a function of temperature (260 – 360°K) and wave-vector (2 × 10⁵ ? 3 × 10⁴cm^?1). Measured magnon energies ranging up to 3.3 cm^?1 (260°K) and line widths are in good agreement with data from microwave resonance work.     

Soldering of Bi-2223/Ag high temperature superconducting tapes with Sn–Pb–Bi–Ag alloy paste

Soldered joints of Bi-2223/Ag-sheathed high temperature superconducting multifilamentary tapes were fabricated using 63 wt.%Sn–34 wt.%Pb–1 wt.%Bi–2 wt.%Ag paste. The soldered joints were observed by scanning electron microscope (SEM) and X-ray diffraction (XRD). Moreover, the electrical properties of joints were evaluated by current–voltage curves, and the tensile strengths of the joints were also tested. The results show that the soldered joint consists of Ag sheath – Ag₃Sn compound layer – PbSn₂ and Ag₃Sn solder layer – Ag₃Sn compound layer – Ag sheath. The joints are obeyed with Ohms Law and the magnitude of the joint resistance, which deceases with the increase of the overlap length, can reach the order of 10^?8 Ω. The tensile strength of the joints with a brittle fracture mode is a little lower than that of the original tapes.     

Semiconducting properties of CoO thin films

This paper reports electrical properties of CoO thin films of different thickness in the range 0.375 – 7.95 μm. Both electrical conductivity and thermopower were measured at elevated temperatures (1223 – 1423 K) and under controlled oxygen partial pressure (5 − 2.1x10⁴ Pa). It was found that at low p(O₂) the electrical conductivity decreases with film thickness. The activation energy of the electrical conductivity (E_a) in air decreases with the oxide thickness from 0.56 eV at 0.375 μm to 0.52 eV for massive CoO while at low p(O₂)=5 Pa the E_a is independent of the thickness (E_a = 0.46 eV). The reciprocal of the p(O₂) exponent of the electrical conductivity (n_δ) in the range 1223 K – 1373 K is close to four for the 7,95 μm film and is about 3.5–3.7 for the 0.375 μm film. The electrical properties of the CoO thin films are considered assuming different defect structures in the bulk phase and the surface layer.     

Simultaneous enhancement in coercivity and remanence of Nd2Fe14B permanent magnet by grain boundary diffusion process using NdHx

We have successfully developed a Dy-free grain boundary diffusion process with neodymium hydride (NdH_x) alloy to the permanent magnet Nd₂Fe₁₄B powders using hydrogenation – disproportionation – desorption – recombination (HDDR) method. All the diffusion treatments were performed at 700–800 °C for various annealing time under the high vacuum with rotating diffusion method that effectively control the abnormal grain growth. The coercivities of Dy-treated Nd₂Fe₁₄B powders were varied from 9.5 kOe to 13.2 kOe but the remanence was decreased to 8.1 kG (10% reduction) depending on dysprosium hydride (DyH_x) content and diffusion treated time. However, the coercivity and remanence of Dy-free diffusion treated powder have been increased to 12.2 kOe (28.5% enhancement) and 11.1 kG (22% enhancement) at the optimal diffusion treatment (800 °C for 3 h), respectively. This unique simultaneous enhancement is to isolate the magnetic coupling between Nd₂Fe₁₄B grains by creating non-magnetic Nd grain boundaries and enhance the alignment of the Nd₂Fe₁4B hard magnetic phase, fabricated by optimal diffusion conditions.