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961.
Vladimir Strezov Artur Ziolkowski Tim J. Evans Peter F. Nelson 《Journal of Thermal Analysis and Calorimetry》2010,100(3):901-907
Ironmaking involves reduction of iron ores to metallic iron using coke, coal or gas as reductants. Although different iron ore reduction processes exist, prior to each reduction type, commonly, the hydroxyl and clay materials present in the iron ores undergo decomposition as a first stage. The mass loss during decomposition of these materials is termed as Loss on Ignition (LOI). The aim of this work is to apply a computer aided thermoanalytical technique to evaluate five different iron ore types during decomposition of the LOI matter and determine associated decomposition temperature ranges and heats of reactions. Fourier Transform Infrared (FTIR) spectroscopy and thermogravimetric analysis (TG) were also incorporated to support the analysis interpretation. Three distinctive temperature ranges of decomposition of iron ore LOI matter were detected. The first region was associated with dehydration of the hygroscopic moisture at a temperature range between 100 and 150 °C. The second region occurred at a temperature range between 260 and 425 °C during which strongly bonded water was released and the OH groups associated with primarily iron oxyhydroxides were fractured. The third range, which occurred at a temperature range of 530 and 605 °C, was related to decomposition of the aluminosilicate clay materials. 相似文献
962.
963.
Zhan C Wang X Wei Z Evans DJ Ru X Zeng X Liu X 《Dalton transactions (Cambridge, England : 2003)》2010,39(46):11255-11262
By using "click" chemistry between a diazide and a diiron model complex armed with two alkynyl groups, two polymeric diiron complexes (Poly-Py and Poly-Ph) were prepared. The two polymeric complexes were investigated using infrared spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermal gravimetric analysis (TGA), M?ssbauer spectroscopy, and cyclic voltammetry (Poly-Py only, due to the insolubility of Poly-Ph). To probe the coordinating mode of the diiron units in the two polymeric complexes, two control complexes (3 and 4) were also synthesised using a monoazide. Complexes 3 and 4 were well characterised and the latter was further crystallographically analysed. It turns out that in both complexes (3 and 4) and the two polymeric diiron complexes, one of the two iron atoms in the diiron unit coordinates with one of the triazole N atoms. Our results revealed that both morphologies and properties of Poly-Py and Poly-Ph are significantly affected by the organic moiety of the diazide. Compared to the protonating behaviour of the complexes 3 and 4, Poly-Py exhibited proton resistance. In electrochemical reduction, potentials for the reduction of the diiron units in Poly-Py and hence its catalytic reduction of proton in acetic acid-DMF shifted by over 400 mV compared to those for complexes 3 and 4. It is likely that the polymeric nature of Poly-Py offers the diiron units a "protective" environment in an acidic medium and more positive reduction potential. 相似文献
964.
Declan Williams Suzanne Ackloo Peihong Zhu Peter Bowden Kenneth R. Evans Christina L. Addison Chris Lock John G. Marshall 《Analytical and bioanalytical chemistry》2010,396(3):1223-1247
The endogenous peptides of human serum may have regulatory functions, have been associated with physiological states, and
their modifications may reveal some mechanisms of disease. In order to correlate levels of specific peptides with disease
alongside internal standards, the polypeptides must first be reliably extracted and identified. Endogenous blood peptides
can be effectively enriched by precipitation of the serum with organic solvents followed by selective extraction of peptides
using aqueous solutions modified with organic solvents. Polypeptides on filter paper were assayed with Coomasie brilliant
blue binding. The polypeptides were resolved by detergent tricine polyacrylamide electrophoresis and visualized by diamine
silver staining. Peptides in the extracts were collected by C18 and analyzed by matrix-assisted laser desorption/ionization
and liquid chromatography–electrospray ionization–tandem mass spectrometry (MS/MS) quadrupole time-of-flight MS/MS. Peptides
were resolved as multiple isotopic peaks in MS mode with mass deviation of 0.1 Da or less and similar accuracy for fragments.
The sensitivity of MS and MS/MS analysis was estimated to be in the picomolar range or less. The peptide composition of the
extracts was dependent on solvent formulation. Multiple peptides from apolipoproteins, complement proteins, coagulation factors,
and many others were identified by X!Tandem with high mass accuracy of peptide ions and fragments from collision-induced dissociation.
Many previously unreported posttranslational modifications of peptides including phosphorylations, oxidations, glycosylations,
and others were detected with high mass accuracy and may be of clinical importance. About 4,630 redundant peptides were identified
with 99% confidence separately, and together some 1,251 distinct proteins were identified with 99% confidence or greater using
the Paragon algorithm. 相似文献
965.
Bodzon-Kulakowska A Suder P Drabik A Kotlinska JH Silberring J 《Analytical and bioanalytical chemistry》2010,398(7-8):2939-2942
Glutamine synthetase is a key enzyme which has a regulatory role in the brain glutamate pool. According to previously published proteomic analysis, it was shown that the expression level of this enzyme is affected by morphine administration. In our study, we examined the activity of glutamine synthetase in various structures of rat brain (cortex, striatum, hippocampus and spinal cord) that are biochemically and functionally involved in drug addiction and antinociception caused by morphine. We were not able to observe any significant changes in the enzyme activity between morphine-treated and control samples despite previously reported changes in the expression levels of this enzyme. These findings stressed the fact that changes observed in the expression of particular proteins during proteomic studies may not be correlated with its activity. 相似文献
966.
Anna K. Renfrew Alexander E. Egger Rosario Scopelliti Christian G. Hartinger Paul J. Dyson 《Comptes Rendus Chimie》2010,13(8-9):1144-1150
Metal complexes bearing phosphine ligands are attracting increasing attention for their applications in medicinal chemistry. In particular, organometallic ruthenium-phosphine complexes have been found to exhibit promising antitumour activity. The synthesis, anticancer activity and reactivity of a novel bis-phosphine complex, [Ru(η6-cymene)(PPh2(o-C6H4O)-κ2-P,O)(pta)]Cl (pta = 1,3,5-triaza-7-phosphatricyclo[3.3.1.1.]decane), is presented. The complex appears to exhibit its anticancer effect via a different mechanism to other ruthenium-arene pta complexes with labile co-ligands. 相似文献
967.
Uranium-carbon bond reactivity has been investigated with the bis(tethered silylalkyl) uranium metallocene (η5:κ1-C5Me4SiMe2CH2)2U, 1. Tert-butyl nitrile, tBuCN, inserts into both of the tethered U-C bonds to produce the bis(tethered ketimide) complex [η5:κ1-C5Me4SiMe2CH2C(tBu)N]2U, 2, which has unusually bent U-N-C bond angles. Carbon dioxide also inserts into both U-C bonds of 1 yielding the bis(tethered carboxylate) (C5Me4SiMe2CH2CO2)2U, 3. Neither PhCCPh nor PhCCH insert into the U-C bonds, but PhCCH cleaves the silylalkyl tethers in 1 to generate (C5Me4SiMe3)1? ligands in the complex (C5Me4SiMe3)2U(CCPh)2, 4. 相似文献
968.
The merits and limitations of gas-phase electron diffraction as a technique for determining accurately the structures of small
organic molecules are demonstrated by comparing the molecular structures of five benzene derivatives studied in two different
laboratories. The existence of many possible representations of the structure of a molecule (r
a, r
g, r
α, r
α0, r
e, …), implying differences in the physical meaning of geometrical parameters, is discussed in some detail as it may cause
difficulties in a comparison. Also illustrated are different ways of estimating and expressing uncertainties in the geometrical
parameters from a gas-phase electron diffraction study. 相似文献
969.
Anna Śmiechowska Witold Przychodzeń Jarosław Chojnacki Piotr Bruździak Jacek Namieśnik Agnieszka Bartoszek 《Structural chemistry》2010,21(5):955-964
Adducts of natural allyl, phenethyl, and benzyl isothiocyanates and 2-amino-1-methylbenzimidazole were synthesized. After
optimization of the reaction conditions, the target 2-benzimidazolylthioureas were obtained in reasonable yields. The detailed
molecular and crystal structures of these compounds were characterized by spectroscopic and X-ray methods. Spectral analysis
demonstrated that N-(1-methylbenzimidazolyl)-N′-allylthiourea, N-(1-methylbenzimidazolyl)-N′-benzylthiourea, and N-(1-methylbenzimidazolyl)-N′-phenethylthiourea exist in solution in an unprecedented three tautomeric forms, whose structures were corroborated unambiguously. 相似文献
970.
Yue Zhu Min Pu De-Cai Fang Yong-Qiang Ji Jing He David G. Evans 《Structural chemistry》2010,21(4):817-825