Leaching Stability and Redox Activity of Copper-MFI Zeolites Prepared by Solid-State Transformations: Comparison with Ion-Exchanged and Impregnated Samples.

The catalyst preparation route is well known to affect the copper loading and its electronic state, which influence the properties of the resulting catalyst. Electronic states of copper ions in copper-containing silicalites with the MFI-framework topology obtained by a solid-state transformation S (SST) were studied with using EPR, UV-Vis DR, XRD, H-TPR and chemical differentiating dissolution. They were compared with Cu-ZSM-5 and Cu-MFI (silicalite) prepared via the ion-exchange and incipient wetness impregnation.

One-pot synthesis of sorbitol via hydrolysis-hydrogenation of cellulose in the presence of Ru-containing composites.

The aim of this work was to study the one-pot synthesis of sorbitol via hydrolysis-hydrogenation of cellulose in the presence of Ru-containing composites based on HPWO supported on ZrO and NbO (Ru-PW/ZrO and Ru-PW/NbO). The main parameters impacted the reaction rate and yield of sorbitol, i.e.

Production of biodiesel and succinic acid from the biomass of the microalga Micractinium sp. IC-44.

In this study, a combined approach to produce fatty acid methyl esters (FAMEs) and succinic acid from the biomass of the microalga Micractinium sp. IC-44 using ionic liquids (ILs) was presented. After 22 days of cultivation, the biomass productivity was 0.

One-pot synthesis of formic acid hydrolysis-oxidation of potato starch in the presence of cesium salts of heteropoly acid catalysts.

Solid bifunctional catalysts based on cesium salts of V-containing heteropoly acids (CsHPA: CsHPWVO, CsHSiWVO, CsHPMoVO) and CsHPMoO were used for studying one-pot hydrolysis-oxidation of potato starch to formic acid at 413-443 K and 2 MPa air mixture. It was shown that the optimum process temperature that prevents formic acid from destruction is 423 K. The studies were focused on the influence of the composition of heteropoly anions on the yield and selectivity of formic acid.

Spontaneous Resolution and Super-coiling in Xerogels of the Products of Photo-Induced Formose Reaction.

This work addresses the supramolecular self-organization in the xerogels of formose reaction products. The UV-induced formose reaction was held in over-saturated formaldehyde solutions at 70C without a catalyst. The solutions of the obtained carbohydrates were dried on a glass slide, and the obtained xerogels demonstrated a prominent optical activity, while the initial solutions were optically inactive.

Colloidal Fe , Mn , Co , and Cu Hydroxides Stabilized by Starch as Catalysts of Water Oxidation Reaction with One Electron Oxidant Ru(bpy).

Colloidal catalysts for oxidation of water to dioxygen, which are stable on storage and under the reaction conditions, are synthesized based on Co , Mn , Fe and Cu hydroxides. Stabilization of the colloids with dextrated starch allows the process of hydroxide ageing to be stopped at the stage of the formation of primary nuclei (ca. 2-3 nm from transmission electron microscopy data).

Highly Stable Single-Atom Catalyst with Ionic Pd Active Sites Supported on N-Doped Carbon Nanotubes for Formic Acid Decomposition.

Single-atom catalysts with ionic Pd active sites supported on nitrogen-doped carbon nanotubes have been synthesized with a palladium content of 0.2-0.5 wt %.

Deuterium Oxide Enhances Escherichia coli SOS Response Induced by Genotoxicants.

It has been demonstrated that deuterium oxide enhances the SOS response of Escherichia coli cells induced by chemical genotoxicants and mutagens. This demonstrates that the heavy nonradioactive hydrogen isotope deuterium can be considered to be a comutagen.

Cloning, expression and characterization of the esterase estUT1 from Ureibacillus thermosphaericus which belongs to a new lipase family XVIII.

A new esterase gene from thermophilic bacteria Ureibacillus thermosphaericus was cloned into the pET32b vector and expressed in Escherichia coli BL21(DE3). Alignment of the estUT1 amino acid sequence revealed the presence of a novel canonical pentapeptide (GVSLG) and 41-47% identity to the closest family of the bacterial lipases XIII. Thus the esterase estUT1 from U.

Screening and comparative metabolic profiling of high lipid content microalgae strains for application in wastewater treatment.

New strains of green microalgae were isolated and screened for growth and the production of lipids from municipal wastewater. It was shown that the strain Micractinium sp. IC-76 has a biomass productivity of 37.

Cellulose Biorefinery Based on a Combined Catalytic and Biotechnological Approach for Production of 5-HMF and Ethanol.

In this study, a combination of catalytic and biotechnological processes was proposed for the first time for application in a cellulose biorefinery for the production of 5-hydroxymethylfurfural (5-HMF) and bioethanol. Hydrolytic dehydration of the mechanically activated microcrystalline cellulose over a carbon-based mesoporous Sibunt-4 catalyst resulted in moderate yields of glucose and 5-HMF (21.1-25.

Terminology spectrum analysis of natural-language chemical documents: term-like phrases retrieval routine.

Background: This study seeks to develop, test and assess a methodology for automatic extraction of a complete set of 'term-like phrases' and to create a terminology spectrum from a collection of natural language PDF documents in the field of chemistry. The definition of 'term-like phrases' is one or more consecutive words and/or alphanumeric string combinations with unchanged spelling which convey specific scientific meanings. A terminology spectrum for a natural language document is an indexed list of tagged entities including: recognized general scientific concepts, terms linked to existing thesauri, names of chemical substances/reactions and term-like phrases.

Catalytic formation of monosaccharides: from the formose reaction towards selective synthesis.

The formose reaction (FR) has been long the focus of intensive investigations as a simple method for synthesis of complex biologically important monosaccharides and other sugar-like molecules from the simplest organic substrate-formaldehyde. The fundamental importance of the FR is predominantly connected with the ascertainment of plausible scenarios of chemical evolution which could have occurred on the prebiotic Earth to produce the very first molecules of carbohydrates, amino- and nucleic acids, as well as other vitally important substances. The practical importance of studies on the FR is the elaboration of catalytic methods for the synthesis of rare and non-natural monosaccharides and polyols.

Quantitative temperature mapping within an operating catalyst by spatially resolved 27Al NMR.

Spatially resolved NMR is employed to quantitatively map the temperature of a solid catalyst under operating conditions during H(2) oxidation with O(2) over Pt/γ-Al(2)O(3). As this new non-invasive in situ technique utilizes the (27)Al NMR signal of the solid phase, it is suitable for catalyst temperature mapping in both liquid- and gas-phase heterogeneous catalytic processes.

Pyrolysis of heavy hydrocarbons under microwave heating of catalysts and adsorbents.

The main features of high temperature chemical reactions under microwave (MW) heating have been considered. The efficiency of the MW power to heat conversion in a MW cavity is estimated, theoretically and experimentally, for different substances and conditions. The new approaches for MW processing of high-molecular hydrocarbons are proposed: (i) thermal decomposition in contact with microwave absorbing catalyst particles placed into liquid substrate; (ii) cracking of hydrocarbons pre-absorbed inside porous granules under rapid MW heating of adsorbent.

Air detoxification with nanosize TiO2 aerosol tested on mice.

A method for fast air purification using high concentration aerosol of TiO(2) nanoparticles is evaluated in a model chemical catastrophe involving toxic vapors of diisopropyl fluorophosphate (DFP). Mice are used as human model in a closed 100 dm(3) chamber. Exposure of mice to 37 ppm of DFP vapor for 15 min resulted in acute poisoning.

The state of absorbed hydrogen in the structure of reduced copper chromite from the vibration spectra.

The reduction of copper chromite, CuCr(2)O(4), is followed by means of thermogravimetric analysis. The reduced state is studied by means of FT IR spectroscopy, Raman spectroscopy and inelastic neutron scattering. The reduction of copper occurs in two stages: absorption of hydrogen at 250-400 degrees C and dehydration of the reduced state at above 450 degrees C.

Significant influence of Zn on activation of the C-H bonds of small alkanes by Brønsted acid sites of zeolite.

Herein, we analyze earlier obtained and new data about peculiarities of the H/D hydrogen exchange of small C(1)-n-C(4) alkanes on Zn-modified high-silica zeolites ZSM-5 and BEA in comparison with the exchange for corresponding purely acidic forms of these zeolites. This allows us to identify an evident promoting effect of Zn on the activation of C-H bonds of alkanes by zeolite Brønsted sites. The effect of Zn is demonstrated by observing the regioselectivity of the H/D exchange for propane and n-butane as well as by the increase in the rate and a decrease in the apparent activation energy of the exchange for all C(1)-n-C(4) alkanes upon modification of zeolites with Zn.

On the influence of the metal loading on the structure of carbon-supported PtRu catalysts and their electrocatalytic activities in CO and methanol electrooxidation.

PtRu (1:1) catalysts supported on low surface area carbon of the Sibunit family (S(BET) = 72 m(2) g(-1)) with a metal percentage ranging from 5 to 60% are prepared and tested in a CO monolayer and for methanol oxidation in H(2)SO(4) electrolyte. At low metal percentage small (<2 nm) alloy nanoparticles, uniformly distributed on the carbon surface, are formed. As the amount of metal per unit surface area of carbon increases, particles start coalescing and form first quasi two-dimensional, and then three-dimensional metal nanostructures.

In situ (1)H and (13)C MAS NMR kinetic study of the mechanism of H/D exchange for propane on zeolite H-ZSM-5.

The kinetics of hydrogen (H/D) exchange between Brønsted acid sites of zeolite H-ZSM-5 and variously deuterated propanes (propane-d(8), propane-1,1,1,3,3,3-d(6), propane-2,2-d(2)) have been monitored in situ by (1)H MAS NMR spectroscopy within the temperature range of 503-556 K. The contribution of intramolecular hydrogen transfer to the H/D exchange in the adsorbed propane was estimated by monitoring the kinetics of (13)C-labeled carbon scrambling in propane-2-(13)C in situ with (13)C MAS NMR at 543-573 K. Possible mechanisms of the exchange have been verified on the basis of the analysis of the variation of protium concentration in both the methyl and the methylene groups of propane in dependence of the reaction time.

CF2Cl2 decomposition over nanocrystalline MgO: evidence for long induction periods.

CF(2)Cl(2) has been found to react with nanoscale MgO at 325 degrees C and higher temperatures. In excess of the halocarbon, the reaction results in the formation of MgF(2) as a predominant solid product, with CCl(4), and CO(2) formed as the main gaseous products. The kinetics of the process is characterized by a prolonged induction period, which is as long as 8.

Mechanism studies of the conversion of 13C-labeled n-butane on zeolite H-ZSM-5 by using 13C magic angle spinning NMR spectroscopy and GC-MS analysis.

By using 13C MAS NMR spectroscopy (MAS = magic angle spinning), the conversion of selectively 13C-labeled n-butane on zeolite H-ZSM-5 at 430-470 K has been demonstrated to proceed through two pathways: 1) scrambling of the selective 13C-label in the n-butane molecule, and 2) oligomerization-cracking and conjunct polymerization. The latter processes (2) produce isobutane and propane simultaneously with alkyl-substituted cyclopentenyl cations and condensed aromatic compounds. In situ 13C MAS NMR and complementary ex situ GC-MS data provided evidence for a monomolecular mechanism of the 13C-label scrambling, whereas both isobutane and propane are formed through intermolecular pathways.

Noninvasive in situ visualization of supported catalyst preparations using multinuclear magnetic resonance imaging.

Multinuclear magnetic resonance imaging (MRI) is employed as a new noninvasive tool for monitoring supported catalyst preparation by visualizing precursor transport within the porous support. In particular, liquid phase 31P MRI experiments were used to visualize the dynamics of H3PO4 penetration into an alumina pellet and have revealed a strong interaction of H3PO4 with the support. Solid state 31P MRI was applied to map the distribution of the adsorbed phosphate inside the support after its drying.