Attempts to Exchange Iron into H-Y and H-ZSM-5 Zeolites by in situ Formed Chloride-Containing Mobile Species

Three variants of solid-state ion exchange were studied. Iron exchange was found to proceed in the first case, in theFeCl₂+NH₄ZSM-5 FeZSM-5 + NH₄Cl process, even at low exchange capacity (Si/Al = 25).The second, Fe₂O₃ (hematite) + HZ direct reaction does not result in any noticeable interaction for eitherZ = Y or ZSM-5. This process can significantly be promoted by introducing CCl₄ vapor via forming chlorine-containingmobile species. However, the structure of the Y zeolite largely collapses during this treatment, whereas the crystalline state of ZSM-5is preserved.     

Synthesis of D-Glucose-based Azacrown Ethers with Phosphinoxidoalkyl Side Chains and Their Application to an Enantioselective Reaction

Five chiral -D-glucose-based monoaza-15-crown-5 ethers with phosphinoxidoalkyl side chains of one to five carbon atoms (5a–e)have been synthesised. The cation binding ability of the new lariat ethers was evaluated bythe picrate extraction method. The substituents at the nitrogen atom were not a major influenceon the cation extraction ability of the azacrown ether; the compounds showed, however, a significant asymmetric induction as phase transfer catalysts in the Michael addition of2-nitropropane to chalcone (95% ee).     

Dedekind Complete Commutative BCK-algebras

We study Dedekind complete commutative BCK-algebras with the relative cancellation property and their connection with corresponding universal groups. We shall characterize Dedekind orthogonally complete atomic and Archimedean BCK-algebras, generalizing results of Jakubík known for MV-algebras. Finally, we characterize those Dedekind complete and atomic commutative BCK-algebras that are isomorphic to direct products of basic BCK-chains, generalizing a result of Cignoli for MV-algebras.     

Morphological and chemical characterization of weathering products on buried Sasanian glass from central Iraq

This paper discusses the morphological and chemical features of the weathering products on Sasanian glass finds excavated at the ancient Sasanian town of Veh Arda?īr, some 30 km south of Baghdad (Iraq), and dated from the third to the sixth century. All the considered fragments represent soda-lime glass, with MgO contents between 3% and 8%, resulting from the use of soda-rich plant ash as a flux; within this general frame, two productions can be distinguished due to their MgO to K₂O ratio. Four main alteration typologies were observed by visual examination of the excavated samples; these were studied by scanning electron microscopy, energy dispersive X-ray analysis, inductively coupled plasma-mass spectrometry, X-ray diffraction and thermal analysis. Different alteration features were generally observed for samples belonging to the two compositional groups. In particular, samples with higher MgO to K₂O ratios show definitely thinner crusts, associated with alteration plugs going down into the glass. Moreover, gray or black crusts are related to the presence of manganese at significant levels in the original glass.     

Chemically Treated Silver Electrodes for the Determination of Cysteine

 This paper describes the use of Ag/Ag₂S and Ag/AgI ion-selective electrodes by means of chemical pretreatment of a silver wire or tube for the determination of cysteine (RSH) in batch and flow injection analysis (FIA). Received December 15, 2000. Revision July 11, 2001.     

Langmuir–Blodgett films of pyridinium-dicyanomethanide dyes mixtures with photobleachable absorption bands

We report on Langmuir-Blodgett (LB) films characterization of 4-[5-dicyanomethanido)thien-2-y1]-N-(n-hexadecyl)pyridinium (C₁₆H₃₃-PDCNT), and 1-(N-(n-hexadecy]-4-pyridinio)-2-[5-(dicyanomethanido)thien-2-yl]ethene (C₁₆H₃₃-PDCNTE); LB films of the pure compounds and of the mixtures of the two compounds were prepared at 291 K: UV-vis investigation revealed the presence of photobleachable absorption bands, the ones at about 530 nm and 640 nm were due to charge transfer transitions of the monomer of C16H33-PDCNT and C₁₆H₃₃-PDCNTE, respectively; the sharp, photobleachable ones shifted to shorter wavelengths were due to H-aggregates of the two compounds. By changing the molar ratios of the two compounds in the mixtures and in other cases by annealing the LB films, the absorption maxima of the sharp, photobleachable bands due to H-aggregates could be tuned in the range 415–467 nm. These LB films are thus very promising in view of optical data storage applications.