Local canted spin behaviour in Co1.4−x Zn x Ge0.4Fe1.2O4 spinels: A macroscopic, mesoscopic and microscopic study

DC magnetization, neutron depolarization and neutron diffraction (with both polarized and unpolarized neutrons) measurements have been reported for the Co_1.1−x Zn _x Ge_0.1Fe_1.2O₁ spinels with x=0.5, 0.6 and 0.7. Neutron depolarization and neutron diffraction measurements confirm the presence of a long range ferrimagnetic ordering of the local canted spins in these ferrite samples. The observed features of low field magnetization have been explained under the framework of thermally activated domain wall movement of ferrimagnetic arrangement of local canted spins. An important role of magnetic anisotropy (due to the presence of Co²⁺ ions) in establishing the magnetic ordering and domain kinetics in these ferrites has been observed.     

Synthesis and luminescence of La2BaZnO5 phosphors

A modified synthesis of La₂BaZnO₅ phosphors activated with rare earths Eu³⁺, Tb³⁺, Pr³⁺ and Sm³⁺, and ns² ion Bi³⁺ is reported. RE₂BaZnO₅ compounds are conventionally prepared by two step solid state reaction. In the first step, carbonates or similar precursors are intimately mixed and heated at 900 °C to decompose the precursors to oxides. To eliminate the unwanted phases like BaRE₂O₄, the resulting powders are reheated at 1100 °C for long time. We prepared La₂BaZnO₅ phosphors activated with various activators by replacing the first step by combustion synthesis. Results on photoluminescence are presented. PL results on Eu³⁺ and Tb³⁺ are in good agreement with the literature reports. PL emission from Sm³⁺, Pr³⁺ and Bi³⁺ had not been reported earlier. Excitation spectrum of Eu³⁺ is dominated by a charge transfer band around 318 nm, while for the other rare earths a band at 240 nm is always present. This is attributed to the host absorption.     

A simple model for a two-stage chemical reaction with diffusion

We analyse the evolution of a two-stage chemical reaction betweentwo neighbouring plumes of reactants. Under the assumption thatthe plumes are approximately Gaussian we derive a system ofordinary differential equations for the total amount, the centroidand the variance of each reactant. We compare the solution ofthese equations with full numerical simulation of the reaction.Excellent agreement is obtained, with solution of the near-Gaussianmodel requiring considerably less computational effort thanthe full simulations. Of key importance is the yield of thereaction, and we discuss this feature in particular.     

Evaluation of bias,precision, and systematic errors in proficiency testing of Cl<Superscript>−</Superscript> and Cu concentration in water

The proficiency testing exercise was conducted to assess the quality of water testing in several laboratories in India. The 11 participants from all over India gathered at one place and attended the workshop organized at NEERI, Nagpur. The test samples were analyzed for Cl⁻ (Chloride) and Cu (Copper) concentration in water. The objective of the study was to determine bias and precision among participants for the analysis of Cl⁻ and Cu concentration. Statistical analysis indicated that most of the measurement results were overestimating the Cl⁻ concentration and underestimating the Cu concentration. The presence of systematic error identified the need for further improvement in determining the Cu concentration in water by the participants.     

Gas-phase deprotonation of arylalkylamines. A collision-induced dissociation study

The collision-induced dissociation (CID) of deprotonated arylalkylamines of general formula R(1)C(6)H(4)CHR(2)CH(2)NR(3)(2) (where R(1) = H, OH, F or NO(2); R(2) = H or OH; R(3) = H or CH(3)) generated by negative chemical ionization with H(2)O and D(2)O as ionizing reagents, is discussed. The negative chemical ionization mass spectra show that, in the absence of a hydroxy group in the aromatic ring, deprotonation takes place at the benzylic position whereas the proton is lost from the OH group when present. The nitro compound forms only M(-.) ions. The CID spectra of the deprotonated molecules show that fragmentations are strongly dependent on the structural features of the molecules, namely the presence or absence of substituents in the aromatic ring or aliphatic chain. Copyright 1999 John Wiley & Sons, Ltd.     

Preparation and characterization of LiAEAlF6:Eu (AE=Mg, Ca, Sr or Ba) phosphors

Wet chemical synthesis of LiAEAlF₆:Eu (AE=Mg, Ca, Sr or Ba) phosphors is described. Formation of single-phase compounds LiCaAlF₆ and LiSrAlF₆ was confirmed by XRD. LiCaAlF₆:Eu and LiSrAlF₆:Eu phosphors exhibited broadband emission corresponding to intraconfigurational transition 4f⁶5d¹→4f⁷(⁸S_7/2). LiMgAlF₆:Eu exhibits a narrow line emission corresponding to ⁶P_J→⁸S_7/2 transition of 4f⁷ configuration besides the band emission. LiBaAlF₆:Eu, on the other hand, was found to yield predominantly line emission.     

Solid state metathesis of CaSO4:Eu2+ phosphor

CaSO₄:Dy, is a well known phosphor for radiation dosimetry using thermoluminescence. CaSO₄:Eu³⁺ and CaSO₄:Eu²⁺ phosphors also find applications in radio-photoluminescence dosimetry and photoluminescent liquid crystal displays (PLLCD), respectively. Various syntheses of these phosphors are known. In this paper solid state metathesis of CaSO₄:Eu using domestic microwave oven is described for the first time. The synthesis is fast, the entire process being completed within few minutes. The phosphor is characterized using XRD and PL techniques.     

Steering in computational science: Mesoscale modelling and simulation

This paper outlines the benefits of computational steering for high performance computing applications. Lattice-Boltzmann mesoscale fluid simulations of binary and ternary amphiphilic fluids in two and three dimensions are used to illustrate the substantial improvements which computational steering offers in terms of resource efficiency and time to discover new physics. We discuss details of our current steering implementations and describe their future outlook with the advent of computational grids.     

空气中激光烧蚀Cu产生等离子体发射光谱的研究

利用Q-开关Nd:YAG激光器产生的1.06 μm、10 ns的脉冲激光聚焦在空气中的Cu靶上,观测了激光诱导的Cu等离子体发射光谱.采用不同的激光能量,分析了波长范围为440 nm到540 nm的空间分辨发射光谱.在局部热力学平衡(LTE)条件近似下,根据谱线的相对强度,得到了等离子体电子温度约在104 K以上,给出了靶面附近电子温度的空间演化规律,并探讨了N(Ⅱ)500.52 nm谱线的谱线强度和半高全宽随激光能量的变化规律.