Effect of annealing temperature on hardness, thickness and phase structure of carbonitrided 304 stainless steel

Carbonitriding of AISI 304 austenitic stainless steel was performed at a plasma-processing power of 450 W using inductively coupled radio frequency (rf) plasma in a gas mixture of 50% N₂ and 50% C₂H₂. The rate of carbonitriding, microhardness, phase structure of the compound layer, surface microstructure and cross-section morphology were studied before and after the annealing process. At the annealing temperature up to 800°C, the microhardness values of the compound zones decrease, while the associated values of the diffused zones increase. Little change was found in the thickness of the compound and diffused zones when the carbonitrided samples were annealed up to 400°C. However, at a higher annealing temperature, the thicknesses of both zones increase. The γ-Fe austenite is the main crystalline phase that can be detected by X-ray diffraction. As the annealing temperature increases up to 500°C, X-ray spectra show α-Fe and Fe₅C₂ phases. Nitrogen diffuses more deeply from the near surface to the interior of the treated sample as the annealing temperature increases up to 800°C and this might explain the extent of carbonitrided thickness and the enhanced microhardness of the diffused zone.     

Comparative vapour phase FTIR spectra and vibrational assignment of manganese pentacarbonyls derivatives of the type XMn(CO)5: (where X=Br, Cl, I, H, D, CH3, CD3, CF3)

The infrared spectra of pure Mn(CO)(5)X in the region 4000-400 cm(-1) has been obtained in the vapour phase. The observed spectrum has been analyzed to distinguish the fundamental frequencies, the rotational-vibrational and structure, and overtone and combination frequencies. The assignment of the observed vapour phase frequencies to the fundamental modes of vibration has been made on C(4V) symmetry. The weak peaks due to XMn(CO)(4)((13)CO) molecules have been measured and assigned for all molecules. This study provides a comprehensive comparison of these compounds, with all of these data the assignment of frequencies is reviewed and a set of quite unambiguous assignments made. The significant finding in this regards are that, it is not necessary to assume lower than C(4V) symmetry for XMn(CO)(5) as has been done in previous consideration of some infrared spectrum of these compounds.     

Separation of no-carrier-added radioactive scandium from neutron irradiated titanium

In this work, sorption of Ni(II) from aqueous solution to goethite as a function of various water quality parameters and temperature was investigated. The results indicated that the pseudo-second-order rate equation fitted the kinetic sorption well. The sorption of Ni(II) to goethite was strongly dependent on pH and ionic strength. A positive effect of HA/FA on Ni(II) sorption was found at pH < 8.0, whereas a negative effect was observed at pH > 8.0. The Langmuir, Freundlich, and D-R models were applied to simulate the sorption isotherms at three different temperatures of 293.15 K, 313.15 K and 333.15 K. The thermodynamic parameters (ΔH ⁰, ΔS ⁰ and ΔG ⁰) were calculated from the temperature dependent sorption, and the results indicated that the sorption was endothermic and spontaneous. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation or ion exchange with Na⁺/H⁺ on goethite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH.     

Synthesis of 2-boryl-1,3-butadienes from tributylphosphine stabilized zirconacyclopropenes and alkynes

Boryl zirconacycopropenes stabilized with tributylphosphine react with alkynes (terminal and internal) to give predominately 2-boryl-1,3-butadienes, 5, in 40-81% isolated yields. Products 5 are accompanied by 4-boryl-1,3-butadienes in 7-23% when terminal alkynes are inserted. However, the use of an internal alkyne (3-hexyne) gave predominantly 6c.     

Novel addition reactions of titanacycle phosphonates by tuning of Ti(O-i-Pr)4/2i-PrMgCl

Di- or tri-substituted vinylphosphonates, 2-5, can be obtained in a highly regio- and stereoselective manner from 1-alkynylphosphonates, by manipulation of Ti(O-i-Pr)4/2i-PrMgCl.     

Surface observation of solvent-impregnated Nafion membrane with atomic force microscopy

Surface morphology modification of the Nafion 117 membrane has been investigated by atomic force microscopy. The effects of water and methanol on the topography and structure of the surface were studied using the contact and tapping atomic force microscopy modes. Nafion topography considerably changes when samples absorb water. However, samples stored in methanol are characterized by flat surfaces. Surface modification was linked to an expansion phenomenon during the swelling of Nafion by solvents. Tapping-mode phase images showed that ionic and cluster domains are distinguishable from the surface of samples impregnated either in water or methanol.     

Indium tellurium trioxide chloride,InTeO3Cl

The new oxy­chloride InTeO₃Cl was synthesized from a mixture of In₂O₃, InCl₃ and TeO₂. Its structure has been determined from single‐crystal X‐ray diffraction data. The structure is composed of layers separated by a van der Waals gap. The layers consist of edge‐sharing chains of [InO₄Cl₂] octahedra linked through [TeO₃] trigonal pyramids. No free Cl atoms are located between the layers.     

Kinetics of thermal dehydration of some bis-(4-aminosalicylato)-diaquo complexes of transition metal ions

The kinetics of thermal dehydration of bis-(4-aminosalicylato)-diaquo complexes of VO(II), Cu(II), Ni(II), Co(II), Fe(II) and Mn(II), were studied. The activation energies and other kinetic parameters have been evaluated. The observed kinetic parameters indicate a first-order reaction. The activation energy of the thermal dehydration decreases in the order: VO(II) > Cu(II) > Co(II) > Ni(II) > Fe(II) > Mn(II), which is also the order for the covalency in the MO bonds.     

One-pot easy conversion of Baylis-Hillman adducts into carbamates of unsaturated β-amino acids

An easy, one-pot transformation of Baylis-Hillman adducts into carbamates of unsaturated β-amino acids, for example, 2-(aryl(methoxycarbonylamino)methyl)acrylic acid methyl esters 7 and 2-(methoxycarbonyl aminomethyl)-3-arylacrylic acid methyl esters 8 via reaction with the Burgess reagent is described.