14 research outputs found
Mathematical model of stacked one-sided arrangement of the burners
Paper is aimed at computer simulation of the turbulent methane-air combustion in upgraded U-shaped boiler unit. To reduce the temperature in the flame and hence NOx release every burner output was reduced, but the number of the burners was increased. The subject of studying: complex of characteristics with space-time fields in the upgraded steam boiler E-370 with natural circulation. The flare structure, temperature and concentrations were determined computationally
Biological Homochirality on the Earth, or in the Universe? A Selective Review
The discovery of meteoritic alpha-amino acids with significant enantiomeric excesses of the L-form has suggested that some cosmic factors could serve as the initial source for chiral imbalance of organic compounds delivered to the early Earth. The paper reviews major hypothesis considering the influence of chiral irradiation and chiral combinations of physical fields on the possible ways asymmetric synthesis and transformations of organics could take place within the solar system. They could result in a small enantiomeric imbalance of some groups of compounds. More attention is paid to the hypothesis on parity violation of weak interaction that was supposed to cause homochirality of all primary particles and a more significant homochirality of compounds directly synthesized from the latter in a plasma reactor. The first experiment with material synthesized in a plasma torch resulting from a super-high-velocity impact showed formation of alanine with the excess of L-form between 7 and 25%. The supposed conclusion is that L-amino acids could serve as a starting homochiral biomolecular pool for life to emerge all over the Universe
Critical review on the origin of atmospheric oxygen: Where is organic matter?
In a short note of 1998 Davankov questioned the generally accepted notion that the unique features of the planet Earth, namely, the presence of life and atmospheric oxygen are inseparably bonded as a case and effect. Indeed, photosynthesis in terrestrial and aquatic phototrophs simultaneously produces oxygen and carbohydrates in almost equal amounts. Since the degradation of organic matter through burning or rotting also consumes an equivalent amount of oxygen, the total masses of oxygen and organic material must always remain comparable. This correlation for Earth appears to be drastically distorted in favor of oxygen, thus disproving the still widespread delusion of biogenic origin of atmospheric oxygen. Instead, by analyzing more recent data on the balance between oxygen and organics we arrive at the conclusion that radiolysis of water vapors with the preferential dissipation of hydrogen to space, most probably, was the major source of the free and oxidation-spent oxygen. The present review tries to illuminate the most important uncertainties that still remain to be clarified before an interdisciplinary and scientifically-balanced picture on the evolution of Earth gets settled
Retention parameters in chromatography (IUPAC recommendations 2001)
Contiene :
Part A.Hold-up volume concept in column chromatography
Part B.Retention parameters in gas chromatographyThe paper presents a revision of terms in the IUPAC "Nomenclature for Chromatography", Pure and Applied Chemistry, 65, 819-872, 1993. The terms revised pertain to hold-up volumes in gas, liquid, and supercritical-fluid chromatography, as well as to basic retention parameters, especially in gas chromatography. A number of related and derived definitions are described, including definitions of the terms "chromatographic process" and "chromatographic phase system". A number of the original terms were found to be misleading or superfluous, including such terms as corrected retention time, net retention time, total retention volume (time), and specific retention volume at 0 °C, and their use is strongly discouragedPeer reviewe
Reversible Sorptive Preconcentration of Noble Metals Followed by FI-ICP-MS Determination
In this paper, we propose the combined procedure of noble metal (NM) determination, including fire assay, acid digestion, and reversible dynamic sorptive preconcentration, followed by flow-injection ICP-MS. Reversible preconcentration of all NMs was carried out using micro-column packed new PVBC-VP sorbent and elution with a mixture of thiourea, potassium thiocyanate, and HCl, which recovers Pd, Ir, Pt, and Au by 95% and Ru, and Rh by 90%. The proposed procedure was approved using certified reference materials
New P-Chiral polyfluoroalkyl phosphoramidite ligand in asymmetric transformations catalysed by palladium and copper complexes
The First Example of Coordination of a Tricyclic Hydrophosphorane to Platinum(II). X-ray Crystal Structure of an Unusual Platinated Phosphorane
Enantiomeric-Enriched Ferrocenes: Synthesis, Chiral Resolution, and Mathematic Evaluation of CD-chiral Selector Energies with Ferrocene-Conjugates
Enantiomeric-enriched ferrocene-modified pyrazoles were synthesized via the reaction of the ferrocene alcohol, (S)-FcCH(OH)CH3 (Fc = ferrocenyl), with various pyrazoles in acidic conditions at room temperature within several minutes. X-ray structural data for racemic (R,S)-1N-(3,5-dimethyl pyrazolyl)ethyl ferrocene (1) and its (S)-enantiomer (S)-1 were determined. A series of racemic pyrazolylalkyl ferrocenes was separated into enantiomers by analytical HPLC on β- and γ-cyclodextrins (CD) chiral stationary phases. The quantum chemical calculations of interaction energies of β-CD were carried out for both (R)- and (S)-enantiomers. A high correlation between experimental HPLC data and calculated interaction energies values was obtained
Nitro-imidazoles in ferrocenyl alkylation reaction. Synthesis, enantiomeric resolution and in vitro and in vivo bioeffects
Ferrocenylalkyl nitro-imidazoles (4a-h, 5a-h) were prepared via the regiospecific reaction of the α-(hydroxy)alkyl ferrocenes, FcCHR (OH) (1a–h; Fc = ferrocenyl; R = H, Me, Et, Pr, i-Pr, Ph, ortho-Cl-Ph, ortho-I-Ph), with nitro-imidazoles in aqueous organic medium (H2O-CH2Cl2) at room temperature in the presence of HBF4, within several minutes in good yields. X-ray structural data for racemic (R,S)-1-N-(benzyl ferrocenyl)-2-methyl-4-nitroimidazole (5f) were determined. The resulting enantiomers were resolved into enantiomers by analytical HPLC on modified amylose or cellulose chiral stationary phases. The viabilities of 4b, 4d, 5b, 5c in vitro, and in experiments in vivo antitumor effects of 1-N-ferrocenylethyl-4-nitroimidazole (4b) against murine solid tumor system Ca755 carcinoma were evaluated