Méthode de dosage du nickel métallique en présence de composés oxydés de nickel dans des matières complexes (minerals)

During investigations on the behaviour of metallic nickel in HgCl₂-, KCN- and HCl-containing media, it was noticed in certain cases that nickel metal dissolution was achieved, while a mixture of nickel oxides remained absolutely unaltered.The working conditions were determined, and on the basis of the results obtained two methods have been developed for the determination of metallic nickel in the presence of nickel oxides in complex materials, including ores.These methods are described, in detail and the results of the experiments are given: they show that an accuracy of about 5 % can be obtained.     

The Equilibrium and Kinetic Modelling of the Biosorption of Copper(II) Ions on <Emphasis Type="Italic">Cladophora crispata</Emphasis>

The biosorption of Cu(II) ions on Cladophora crispata was investigated as a function of the initial pH, temperature and initial Cu(II) ion concentration. Algal biomass exhibited the highest Cu(II) uptake capacity at 25C and at the initial pH of 4.5. Equilibrium data fitted very well to both the Langmuir and Freundlich isotherm models. The pseudo second order kinetic model was applied to describe the kinetic data and the rate constants were evaluated in the studied concentration range of Cu(II) ions at all the temperatures studied. The experimental data fitted well to the pseudo second order kinetic model with a high correlation coefficient (R² > 0.99), which indicates that the external mass transfer limitations in the system can be neglected and the chemical sorption is the rate-limiting step. The pseudo second order kinetic constants were also used to calculate the activation energy of Cu(II) biosorption.     

Compact fiber-optic fluorosensor employing light-emitting ultraviolet diodes as excitation sources

A compact fluorosensor using three different ultraviolet light-emission diodes as excitation sources for fiber-optic recording of fluorescence spectra from samples is described. A compact integrated spectrometer with linear array wavelength recording is used, yielding a spectral resolution of about 8 nm. In two system implementations ultraviolet light-emitting diodes at 300, 340 and 395 nm, or at 360, 385 and 410 nm were used as excitation sources with typical emission halfwidths of 12 nm, each combined with a matching long-path colored-glass filter automatically brought into the fluorescence light flow for suppression of reflected light. Spectra from measurements on vegetation, human skin tumors and a rare-earth ion-based thermographic phosphor were recorded to illustrate the system performance.     

Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide

N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide in partial cone conformation was selectively synthesized by appropriately controlling the steric effect during the amidation reactions of N-benzylhexahomotriaza-p-chlorocalix[3]tri(ethyl acetate) in cone or partial cone conformations with use of 1-aminomethylnaphthalene. The conformation was confirmed by (1)H, (13)C, and 2D NMR and X-ray single-crystal analysis. Analyses of the complexes revealed that recognition is strongly affected by Cd(2+), Pb(2+), and F(-) ions.     

Synthesis and Characterization of Eight Arylpentazoles

p‐Nitrophenyl‐, p‐methoxyphenyl‐, p‐hydroxyphenyl‐, p‐t‐butylphenyl‐, p‐HOSO₂‐phenyl‐, ¹⁵N‐p‐N,N‐dimethylaminophenyl‐, ¹⁵N₂‐p‐N,N‐dimethylaminophenyl‐, and dicyanoimidazopentazole were obtained via different synthetic routes. Cesium, barium, potassium, and sodium salts of the arylpentazoles bearing acidic hydrogens were prepared. NMR spectra (¹H, ¹³C) are reported for the arylpentazoles, their corresponding arylazides, and their salts.     

How 10 at% Al Addition in the Ti-V-Zr-Nb High-Entropy Alloy Changes Hydrogen Sorption Properties

Al_0.10Ti_0.30V_0.25Zr_0.10Nb_0.25 was prepared to evaluate the effect of 10% aluminum into the previously reported quaternary alloy, Ti_0.325V_0.275Zr_0.125Nb_0.275. The as-cast quinary alloy formed a single-phase body centered cubic solid solution and transformed into a body centered tetragonal after hydrogenation. The alloy had a storage capacity of 1.6 H/M (2.6 wt.%) with fast absorption kinetics at room temperature, reaching full capacity within the first 10 min. The major improvements of Al addition (10%) were related to the desorption and cycling properties of the material. The temperature for hydrogen release was significantly decreased by around 100 °C, and the quinary alloy showed superior cycling stability and higher reversible storage capacity than its quaternary counterpart, 94% and 85% of their respective initial capacity, after 20 hydrogenation cycles without phase decomposition.     

Crystal Structure of Curcumenol: Evidence of Asymmetric O–H...O (bridged) Hydrogen-Bonded Closed Dimer

Curcumenol, C₁₅H₂₂O₂, was isolated from Globba malaccensis Ridl. The compound was crystallized from ethylacetate/hexane solution in the monoclinic system, space group C2, with cell dimensions a = 16.8467(4) , b = 7.6799(2) , c = 11.8613(10) , = 115.9970(10)°. The molecules form a distorted centrosymmetric dimer linked by hydrogen bonds between the hydroxyl O2 atom and the bridged O1 ether atom (O2...O1(–x+2, y, –z+1), 2.8297(15) ; (O2–H2O–O1), 169(2)°). This is an interesting example of an O–H...O (bridged ether) asymmetric hydrogen-bonded dimer.     

Oriented crosslinked polyethylene pipes by a novel extrusion method

Crosslinking and stretching (2.5 times along the circumferential direction) of the molten polymer during extrusion produced pipes with dominantly circumferential orientation and a lower degree of axial chain orientation. Differential scanning calorimetry (crystallinity and crystal thickness), density measurements (crystallinity), X-ray diffraction (c-axis orientation), infrared dichroism measurements (crystalline and amorphous chain orientation) and contraction measurements (molecular draw ratio) assessed the microstructure of the pipe material. The mechanical properties of the oriented material were assessed by uniaxial tensile tests. The orientation was biaxial with the main orientation in the circumferential direction and a lesser orientation in the axial direction. The maximum degree of circumferential orientation was obtained at the inner wall of the pipe. The lower degree of crosslinking of the core material allowed slippage of chains during the stretching of the molten polymer and it is suggested that this is the cause of the lower degree of orientation of the core material. The oriented pipe material exhibited a 5-10% higher degree of crystallinity and higher crystal thickness than conventionally crosslinked material. The tensile modulus and the tensile strength of the oriented, cross-linked material was greater along the axial direction than along the circumferential direction. The circumferential and axial moduli for the oriented, crosslinked pipe were greater than the corresponding moduli of the non-oriented cross-linked pipe material. Another pipe based on crosslinked PE that were first circumferentially stretched 2.5 times and later axially stretched 10 times (in the molten state) showed, despite the fact that it exhibited pronounced axial orientation almost a balanced tensile modulus (4.3±0.2 GPa) in the axial-circumferential plane. Atomistic modelling showed that the orientational dependence of the density of the amorphous phase is small.     

Synthesis of new monofunctional and oligofunctional oxetane acetals

Derivatives of 3‐ethyl‐3‐(hydroxymethyl)oxetane (trimethylolpropane oxetane), potentially useful in cationic UV‐curable formulations, were prepared by the simple acid‐catalyzed addition of alcohols to 1‐alkenyl ethers. Examples include several difunctional oxetane derivatives along with one fluorinated and one acryloylated oxetane derivative. These new materials may find use as reactive diluents or binders in several applications. A preliminary assessment of the curing was made. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 613–619, 2001