New polymer syntheses

Summary Various poly(ether sulfide)s were prepared by polycon-densation of 4-mercaptophenol or silylated 4-mercaptophenol with 2,6-dichloropyridine or 3,6-dichloropyridazine. A two step and an one-pot procedure were compared. The poly-(ether-sulfide)s were characterized by elemental analyses, inherent viscosities, ¹³C-NMR spectroscopy, gel-permeation chromatography and DSC-measurements.     

Convective Regime of Filtration Combustion of Energetic Materials in a Cocurrent Flow of Their Combustion Products

The convective regime of filtration combustion of energetic materials in a cocurrent flow of their combustion products is studied using a model with extremely simplified kinetics and heat transfer, which shows instability of the process. It is shown that the more accurate twotemperature model describes a steadystate regime. In this regime, the gas temperature on the hot boundary of the heating zone is well below the combustion temperature, and the solidphase temperature is well below the temperature proposed in recent studies on this topic. It is pointed out that the twotemperature approach is unjustified and intragranular nonisothermicity must be taken into account for convective regimes. It is shown that the threetemperature model, which takes into account this effect, does not give a stable steadystate solution.     

Variable‐temperature IR spectroscopic studies of CO adsorbed on Na‐ZSM‐5 and Na‐Y zeolites

CO interacts with extraframework alkali metal cations (M⁺=) of zeolites to form both M⁺CO and M⁺OC species. By using variabletemperature FTIR spectroscopy, these Cbonded and Obonded species were found to be in a temperaturedependent equilibrium. For the same cation, the difference in interaction energy depends upon the zeolite framework. Thus, for the equilibrium process ZNa⁺=CO ZNa⁺OC, where Z represents the zeolite framework, H ⁰ was found to take the values 3.8 and 2.4 kJ mol^– for CO/NaZSM5 and CO/NaY, respectively. The Cbonded species show always the highest cation–CO interaction energy.     

Synthesis of statistical polydiene networks by reaction of liquid polyenes with telechelic siloxanes

The present investigation concerns the synthesis of statistical networks similar to vulcanized rubber. We have used liquid precursor polymers: polybutadiene (PB) and polyisoprene (PI) with telechelic siloxanes. The reactivity of the polydienes can be classified as follows: PB units 1,2 PI units 3,4 PI units 1,4 0. The network formation is a function of the ratio R = nb, of pendent double bonds/nb. of SiH. For R 1 the networks are rather hard and brittle, for 8 R 10 they are soft and elastic, whereas for R 16 the gels obtained are very soft and sticky.     

On the structure of the activated iron catalyst for ammonia synthesis

The contribution focuses on a brief account of the activation of iron oxide precursors to ammonia synthesis catalysts and discusses the question as to why normal iron is so inferior in catalytic performance compared to ammonia iron. The combination of microstructural analysis with kinetic observations allows the conclusion that the microtexture of ammonia iron is with a platelet morphology different from isotropic iron. The role of all additives in the generation of the platelet form is examined. The presence of oxygen, which was speculated to be beneficial for the reaction under certain conditions, was found to be detrimental for the catalytic performance under the present testing conditions.     

Location of Mn in MnAPO‐11: influence of synthesis from aqueous and non‐aqueous media

MnAPO11 samples were synthesized from aqueous (MnAPO11(A)) and ethylene glycol (MnAPO11(NA)) media. The crystallinity of the samples was more when the synthesis was carried out in ethylene glycol. Chemical and thermogravimetric analyses reveal greater incorporation of Mn in the framework of MnAPO11(NA) than in MnAPO11(A). At least five different types of Mn(II) species are detected in the samples by ESR. The studies suggest that Mn is more homogeneously distributed in MnAPO11(NA) than in MnAPO11(A).     

Studies on electrical conductivity of gamma irradiated polyaniline

Summary de electrical conductivity at surface of -irradiated polyaniline (PAn) has been studied. EPR spectroscopic results indicate that the variation of spin concentration is consistent with the increase of _de. Electrical conductivity (_de) versus temperature (T) characteristics of unirradiated and irradiated PAn were performed, which demonstrate that the unirradiated curve can fit to ln_deT₁, while the irradiated curve fit to ln_deT_1/4.     

Molybdenum nitride for the direct decomposition of NO

The physico-chemical properties of passivated -Mo₂N have been investigated. The material showed high activities for NO direct decomposition: nearly 100% NO conversion and 95% N₂ selectivity were achieved at 450C. The amount of O₂ taken up by -Mo₂N increased with temperature rise and reached 3133.9 molg^–1 at 450C; we conclude that there formation of Mo₂O_xN_y occurred. This oxygen-saturated -Mo₂N material was catalytically active: NO conversion and N₂ selectivity were 89 and 92% at 450C. We found that by means of H₂ reduction at 450C, Mo₂O_xN_y could be reduced back to -Mo₂N and the oxidation/reduction cycle is repeatable; such a behaviour and the high oxygen capacity (3133.9 molg^–1) of -Mo₂N suggest that -Mo₂N is a promising catalytic material for automobile exhaust purification.     

Change in degree of polyamidation of polycaproamide during orientation stretch

Conclusions The effect of stretch ratio, the ratio of stretch ratios in the cold and hot zones, and of the relative viscosity of polycaproamide on the degree of its breakdown during stretching have been examined.The degree of breakdown decreases if the viscosity stays within the range 3.25–3.35, and the stretch ratio in the cold zone is the maximum possible.Translated from Khimicheskie Volokna, No. 5, pp. 26–27, September–October, 1983.     

Textural and structural studies on nickel hydroxide electrodes. II. Turbostratic nickel (II) hydroxide submitted to electrochemical redox cycling

The textural and structural modifications involved in electrochemical redox cycling of turbostratic nickel (II) hydroxide has been investigated using X-ray diffraction and electron microscopy methods. It was found that during the first cycles, different phenomena compete: redox reactions which occur in the solid state, and ageing reactions via the solution. For the first galvanostatic charge performed at the C/5 rate in 4.5 N KOH, the direct oxidation of (II) to (III) and the ageing of (II) to (II) via the solution followed by the oxidation to (III) are in competition. The study of the discharge mechanism shows that the direct reduction (III)(II) is parallel to the reduction (III)(II) and the ageing of the turbostratic hydroxide via the solution. After the first cycle it was established that the alpha-generated (II) active phase consisted of a mixture of two kinds of particles, the oxidation of which follows two paths: (II)/(III) for the thicker particles and for the thinner (II)/(III), but these latter (II) particles aged via the solution by Oswald ripening and the (II)/(III) couples swung to (II)/(III).     

Possible Ignition of Particles Ejected into the Gap in Explosive Welding of Titanium

Processes that occur in the welding gap during explosive welding are analyzed. It is shown that metal particles flying out into the gap due to the jetformation effect can ignite in shockcompressed air. For most metals, the energy released thereby is small and has no significant influence on weld formation. In titanium welding on large areas, surface sections located far from the place of detonation initiation, which experience a longterm action of a hot air flow, can dissolve a large amount of oxygen and nitrogen. If particles from these sections enter the gap, it can lead to chemical reactions with formation of TiO₂ and TiN by the mechanism of internal combustion. The energy released in the gap per unit area is commensurable with and even greater than the kinetic energy of the accelerated (flyer) plate. Local bulging and rupture of metal observed in practice can be explained by ignition and combustion of gassaturated titanium particles in the welding gap.     

State and prospects of development of domestic equipment for manufacture of needle-punched,nonwoven materials from polymer melts

Conclusions Domestic equipment has been devised for the production of needle-punched nonwoven geotextile materials from second-grade polycaproamide or fibre-forming polypropylene.The geotextile materials produced are promising for use in construction of roads, foundations of buildings, in hydrotechnology, and in land reclamation.Promising trends in the development of equipment for preparing spun nonwoven materials have been noted (light-duty needle-punched or heat-bonded materials, bulky spun articles, etc.).Coworkers of the Kemerovskii and Kamenskii Khimvolokno IAs the Khimtekstil'mash SIA, the VNIISV, the GIPROtyumenneftegaz, the SoyuzdorNII, and the Plastpolimer SIA took part in this work.Translated from Khimicheskie Volokna, No. 4, pp. 8–10, July–August, 1989.     

Defensive steroids from a carrion beetle (Silpha novaboracensis)

Two novel steroids, 3,7-dihydroxy-14-pregn-4-en-15,20-dione (1) and 3,7, 20-trihydroxy-14-pregn-4-en-15-one (4), have been characterized from the rectal gland ofSilpha novaboracensis (Coleoptera: Silphidae). Judging from the function of comparable pregnanes in another species ofSilpha, the compounds may play an antipredator role.Paper No. 81 of the seriesDefense Mechanisms of Arthropods. Paper No. 80 is Eisner, T., Deyrup, M., Jacobs, R., and Meinwald, J.,J. Chem. Ecol. 12:1407–1415.     

Study of the β — α solid-solid transition of isotactic polypropylene by synchrotron radiation

Synopsis The transformation of the -modification into -modification in isotactic polypropylene was investigated by WAXS, DSC and dilatometric methods. The temperature and time dependent WAXS spectra were made by using high-intensity synchrotron radiation. The - transformation was followed by short time exposures. The transformation of the -modification was found to act toward the increase in the total crystallinity.     

Determination of optical purity of substituted β-lactones

An octakis (3-O-butyryl-2,6-di-O-pentyl)--cyclodextrin capillary gas chromatographic column was used to determine the optical purity of seven different -lactones, having substituents in - or -position, and DL-lactide. The resolving power varied from one lactone to another. The optical purity values determined by GC were in agreement with those obtained from NMR spectroscopy or optical rotation.     

Bending behavior of an electrically activated complex forming hydrogel

Summary The complex forming poly[(ethylene glycol-co-proplene glycol)-g-acrylamide]: polyacrylic acid interpenetrating polymer network hydrogel is able to bend under electric field stimuli. pH, ionic strength gradients and voltage can influence it's bending degree. So we may improve the sample' responsive speed through manipulating those factor in the further study in order to put it into the biomedical application.     

Synthesis and characterization of poly(1-sila-cis-pent-3-enes) substituted with pendant pyridinyl groups

Poly[1-methyl-1-[3-(3-pyridinyl)propyl]-1-sila-cis-pent-3-ene], poly[1-phenyl-1-[3-(3-pyridinyl)propyl)-1-sila-cis-pent-3-ene], and poly[1-phenyl-1-(4-pyridinyl)-1-sila-cis-pent-3-ene] were synthesized by the anionic ring-opening polymerization of 1-methyl-1-[3-(3-pyridinyl)propyl]-1-silacyclopent-3-ene, 1-phenyl-1-[3-(3-pyridinyl)propyl]-1-silacyclopent-3-ene, and 1-phenyl-1-(4-pyridinyl)-1-silacyclopent-3-ene, respectively. These are the first polycarbosilanes which contain heterocyclic pyridine units as side-chain substituents. These polymers were characterized by¹H,¹³C, and²⁹Si NMR as well as by IR and UV spectroscopy. The molecular weight distributions were determined by gel permeation chromatography, glass transition temperatures, by differential seanning calorimetry: (DSC) and thermal behavior, by thermogravimetric analysis. (TGA).     

Silphinene Sesquiterpenes as Model Insect Antifeedants

Silphinene sesquiterpenes are established chrysomelid antifeedants. In this work, nine silphinene analogs, 11-acetoxy-5-angeloyloxysilphinen-3-one (1), 11-acetoxy-5-tigloyloxysilphinen-3-one (2), 11-acetoxy-5-iso- butyryloxysilphinen-3-one (3), 11-hydroxy-5-angeloyloxysilphinen-3-one (4), 11,5-dihydroxysilphinen-3-one (5), 11,5-diacetoxysilphinen-3-one (6), 5,11-diisobutyryloxysilphinen-3-one (7), silphinen-3,5,11-trione (8), and O-methyl-5-epicantabrenolic acid methyl ester (10), and a presilphiperfolane sesquiterpene (9) were tested against several divergent insect species, including the lepidopteran Spodoptera littoralis, the chrysomelid Leptinotarsa decemlineata, and five aphid species, and their antifeedant effects were compared with those of picrotoxinin, a GABA-antagonist, and thymol, an allosteric modulator for insect GABA receptors. All insects tested responded to at least one silphinene analog and/or GABA antagonist. Compound 3 and thymol were effective antifeedants against all species tested except S. littoralis, with varying potencies according to their feeding ecologies. The toxicity of these compounds was species-dependent and did not correlate with their antifeedant effect.     

A study of the acidic and catalytic properties of pure and sulfated zirconia–titania and zirconia–silica mixed oxides

Protonated pyridine (PyH⁺) was not found on ZrO₂ (Z) or ZrO₂–TiO₂ (ZT), but was detected on sulfated oxides (ZS, ZTS) by IR spectroscopy. In contrast, ZrO₂–SiO₂ samples containing about 30–80 mol% ZrO₂ showed Brønsted acidity both in nonsulfated (ZS) and sulfated (ZSS) forms. The total acidity was determined by NH₃TPD. Introduction of sulfate ions increased the sitespecific catalytic activity (TOF) in the conversion of cyclopropane or nhexane. The effect of sulfate ions was more significant on samples rich in zirconia. Results suggest that Zr is homogeneously distributed in ZS samples rich in silica. Zirconiabound dimeric sulfate, generating strong acidity, could not be formed in these preparations due to the absence of fairly large ZrO₂ domains.     

Electrochemical behaviour of viologen-cyclodextrin inclusion complexes. The case of non-alkyl group substituted viologen

The electrochemical behavior of non-alkyl substituted viologen, 4,4-dibenzyl bipyridinium (BzV), 4,4-dicyanophenyl bipyridinium (CyV) and -,-,-cyclodextrin (, , -CD) was studied using cyclic voltammetry and a spectroelectrochemical method. It was found that BzV and Fe(CN) ₆ ^4– formed a charge-transfer (CT) complex with a ratio of 21 and the colour of the solution faded with the addition of an electrolyte. This behaviour is the same as in then-heptyl viologen and ferrocyanide system [1]. BzV, -CD and -CD formed an inclusion complex only in the reduced state, whilst BzV and -CD formed an inclusion complex in both the oxidized and the reduced state. An EC scheme in which a chemical reaction follows an electrochemical reaction was considered to predominate in the BzV and -, -CD systems, while a CE scheme in which a chemical reaction preceded an electrochemical reaction predominated in the BzV and -CD system. On the other hand, CyV was found to form an inclusion complex with -, -, -CD in both the oxidized and the reduced states. therefore a CE scheme was considered to predominate in the CyV--, -, -CD systems.