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1.
An experimental study of the thermal decomposition of powdered cellulose and pine sawdust has been performed. The influence of the heating rate on the temperature profiles in the sample and on the solid conversion rate has been studied. A mathematical model without adjustable parameters has been used to calculate the temperature at different points in the solid bed and the average total solid conversion. The experimental results have been compared with those calculated by the model. A good agreement has been obtained for sawdust. Some differences are observed for cellulose at high heating rates, and the influence of the thermal conductivity and the reaction heat on the results has been analysed. 相似文献
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V. A. Dudnikov D. A. Velikanov N. V. Kazak C. R. Michel J. Bartolome A. Arauzo S. G. Ovchinnikov G. S. Patrin 《Physics of the Solid State》2012,54(1):79-83
Temperature and magnetic-field dependences of the static magnetization of polycrystalline cobaltite GdCoO3 have been measured. The magnetic properties of the GdCoO3 sample have been studied in the paramagnetic and antiferromagnetic states. The magnetic phase diagram has been constructed.
The exchange field between the Gd-Gd sublattices and the anisotropy field have been estimated. 相似文献
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Alonso PJ Arauzo AB García-Monforte MA García-Rubio I Martín A Menjón B Rillo C 《Dalton transactions (Cambridge, England : 2003)》2011,40(4):853-861
The homoleptic, square pyramidal organochromium(III) compound [NBu(4)](2)[Cr(C(6)F(5))(5)] (1) reacts with excess organic isocyanides, CNR [R = (t)Bu, 2,6-dimethylphenyl (Xy)], under dissociation of the apical C(6)F(5) ligand to give the more saturated, singly charged complexes [NBu(4)][trans-Cr(C(6)F(5))(4)(CNR)(2)] [R = (t)Bu (2), Xy (3)], containing six monodentate C-donor ligands. These compounds exhibit an axially distorted octahedral structure (single-crystal X-ray diffraction) with the four C(6)F(5) groups defining the equatorial positions and the CNR ligands occupying the axial ones. Compounds 2 and 3 both behave as spin quartet species (S = 3/2) at microscopic level (EPR spectroscopy), their macroscopic magnetic properties depending upon the nature of the terminal R group, as established by magnetisation measurements. When the R substituent is the saturated alkyl group (t)Bu, the compound (2) behaves as a simple paramagnet, with no magnetic interaction between individual Cr(III) centres along the whole temperature range measured (1.8-265 K). By contrast, a weak antiferromagnetic interaction is detected for compound 3 at low temperature with T(N) = 0.19(1) K. Since the closest intermetallic distances are similar in the crystals of 2·CH(2)Cl(2) and 3·1.75CH(2)Cl(2) (ca. 1.1 nm), we conclude that the insaturation of the aromatic Xy group together with the extended intermolecular π-π stacking interactions between Xy rings observed in the crystal lattice of 3·1.75CH(2)Cl(2) (centroid-to-centroid distance: 0.35 nm) favour magnetic interaction between the individual magnetic centres. 相似文献
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Pablo J. Alonso Prof. Dr. Ana B. Arauzo Dr. María Angeles García‐Monforte Dr. Antonio Martín Dr. Babil Menjón Dr. Conrado Rillo Prof. Dr. Milagros Tomás Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(41):11020-11030
Homoleptic perhalophenyl derivatives of divalent nickel complexes with the general formula [NBu4]2[NiII (C6X5)4] [X=F ( 1 ), Cl ( 2 )] have been prepared by low‐temperature treatment of the halo‐complex precursor [NBu4]2[NiBr4] with the corresponding organolithium reagent LiC6X5. Compounds 1 and 2 are electrochemically related by reversible one‐electron exchange processes with the corresponding organometallate(III) compounds [NBu4][NiIII (C6X5)4] [X=F ( 3 ), Cl ( 4 )]. The potentials of the [NiIII (C6X5)4]?/[NiII (C6X5)4]2? couples are +0.07 and ?0.11 V for X=F or Cl, respectively. Compounds 3 and 4 have also been prepared and isolated in good yield by chemical oxidation of 1 or 2 with bromine or the amminium salt [N(C6H4Br‐4)3][SbCl6]. The [NiIII (C6X5)4]? species have SP‐4 structures in the salts 3 and 4 , as established by single‐crystal X‐ray diffraction methods. The [NiII (C6F5)4]2? ion in the parent compound 1 has also been found to exhibit a rather similar SP‐4 structure. According to their SP‐4 geometry, the NiIII compounds (d7) behave as S=1/2 systems both at microscopic (EPR) and macroscopic levels (ac and dc magnetization measurements). The spin Hamiltonian parameters obtained from the analysis of the magnetic behavior of 3 and 4 within the framework of ligand field theory show that the unpaired electron is centered mainly on the metal atom, with >97 % estimated d contribution. Thermal decomposition of 3 and 4 proceeds with formation of the corresponding C6X5? C6X5 coupling compounds. 相似文献
5.
A.I. Figueroa J. Bartolomé J.M. García del Pozo A. Arauzo E. Guerrero P. Téllez F. Bartolomé L.M. García 《Journal of magnetism and magnetic materials》2012
A transverse susceptibility (TS) measurement system based on a simple inverter CMOS cell oscillator cross-coupled to a LC tank is presented. The system has been implemented to operate at a Quantum Design Physical Properties Measurement System (PPMS). We introduce several improvements with respect to similar currently operating TS measurement equipments. The electronics have been redesigned to use CMOS transistors as active devices, which simplifies the circuit design and enlarge the tuning range, thus making the proposed electronic block more feasible, predictable, and precise. Additionally, we propose a newly designed sample holder, which facilitates the procedure to change a sample and improves reproducibility of the circuit. Our design minimizes the thermal leak of the measuring probe by one order of magnitude, allowing to measure from 1.8 K in standard PPMS systems, thanks to the use of a low temperature beryllium–copper coaxial cable instead of the conventional RG402 Cu coaxial cable employed in the insert for the PPMS in similar systems. The data acquisition method is also simplified, so that the measuring sequences are implemented directly in the PPMS controller computer by programming them in the Quantum Design MultiVu software that controls the PPMS. We present the test measurements performed on the system without sample to study the background signal and stability of the circuit. Measurements on a Gd2O3 calibrating sample yield to the estimation of the system sensitivity, which is found to be on the order of 10−6 emu. Finally, measurements on a TmCo2 Laves phase sample with a ferrimagnetic transition temperature around 4 K are described, demonstrating that the developed system is well suited to explore interesting magnetic phenomena at this temperature scale. 相似文献
6.
Dr. Ana Arauzo Prof. Javier A. Cabeza Prof. Israel Fernández Dr. Pablo García-Álvarez Dr. Inés García-Rubio Dr. Carlos J. Laglera-Gándara 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(15):4985-4992
The reactivity of the PGeP germylene 2,2’-bis(di-isopropylphosphanylmethyl)-5,5’-dimethyldipyrromethane-1,1’-diylgermanium(II), Ge(pyrmPiPr2)2CMe2, with late first-row transition metal (Fe-Zn) dichlorides has been investigated. All reactions led to PGeP pincer chloridogermyl complexes. The reactions with FeCl2 and CoCl2 afforded paramagnetic square planar complexes of formula [MCl{κ3P,Ge,P-GeCl(pyrmPiPr2)2CMe2}] (M=Fe, Co). While the iron complex maintained an intermediate spin state (S1; μeff=3.0 μB) over the temperature range 50–380 K, the effective magnetic moment of the cobalt complex varied linearly with temperature from 1.9 μB at 10 K to 3.6 μB at 380 K, indicating a spin crossover behavior that involves S1/2 (predominant at T<180 K) and S3/2 (predominant at T>200 K) species. Both cobalt(II) species were detected by electron paramagnetic resonance at T<20 K. The reaction of Ge(pyrmPiPr2)2CMe2 with [NiCl2(dme)] (dme=dimethoxyethane) gave a square planar nickel(II) complex, [NiCl{κ3P,Ge,P-GeCl(pyrmPiPr2)2CMe2}], whereas the reaction with CuCl2 involved a redox process that rendered a mixture of the germanium(IV) compound GeCl2(pyrmPiPr2)2CMe2 and a binuclear copper(I) complex, [Cu2{μ-κ3P,Ge,P-GeCl(pyrmPiPr2)2CMe2}2], whose metal atoms are in tetrahedral environments. The reaction of the germylene with ZnCl2 led to the tetrahedral derivative [ZnCl{κ3P,Ge,P-GeCl(pyrmPiPr2)2CMe2}]. 相似文献
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Amran AB Majid Aznan Fazli Ismail Muhamad Samudi Yasir Redzuwan Yahaya Ismail Bahari 《Journal of Radioanalytical and Nuclear Chemistry》2013,297(2):277-284
Previous studies have shown that the natural radioactivity contained in building materials have significantly influenced the dose rates in dwelling. Exposure to natural radiation in building has been of concerned since almost 80 % of our daily live are spend indoor. Thus, the aim of the study is to assess the radiological risk associated by natural radioactivity in soil based building materials to dwellers. A total of 13 Portland cement, 46 sand and 43 gravel samples obtained from manufacturers or bought directly from local hardware stores in Peninsular of Malaysia were analysed for their radioactivity concentrations. The activity concentrations of 226Ra, 232Th and 40K in the studied building materials samples were found to be in the range of 3.7–359.3, 2.0–370.8 and 10.3–1,949.5 Bq kg?1 respectively. The annual radiation dose rates (μSv year?1) received by dwellers were evaluated for 1 to 50 years of exposure using Resrad-Build Computer Code based on the activity concentration of 226Ra, 232Th and 40K found in the studied building material samples. The rooms modelling were based on the changing parameters of concrete wall thickness and the room dimensions. The annual radiation dose rates to dwellers were found to increase annually over a period of 50 years. The concrete thicknesses were found to have significantly influenced the dose rates in building. The self-absorption occurred when the concrete thickness was thicker than 0.4 m. Results of this study shows that the dose rates received by the dwellers of the building are proportional to the size of the room. In general the study concludes that concrete building materials; Portland cements, sands, and gravels in Peninsular of Malaysia does not pose radiological hazard to the building dwellers. 相似文献
10.
Sudharshan Prabhu Rekha PD Chiu-Chung Young Asif Hameed Shih-Yao Lin Arun AB 《Applied biochemistry and biotechnology》2013,171(4):817-831
Zeaxanthin carotenoids are class of commercially important natural products and diverse biomolecules produced by plants and many microorganisms. Bacteria often produce a cocktail of polar and nonpolar carotenoids limiting their industrial applications. Marine members of the family Flavobacteriaceae are known to produce potential carotenoids such as astaxanthin and zeaxanthin. A few bacterial species have been reported for the predominant production zeaxanthin. Here, we report the molecular identification of the zeaxanthin as a major carotenoid produced by two novel bacteria (YUAB-SO-11 and YUAB-SO-45) isolated from sandy beaches of South West Coast of India and the effect of carbon sources on the production of zeaxanthin. The strains were identified based on the 16S rRNA gene sequencing as a member of genus Muricauda. The closest relatives of YUAB-SO-11 and YUAB-SO-45 were Muricauda aquimarina (JCM 11811T) (98.9 %) and Muricauda olearia (JCM 15563T) (99.2 %), respectively, indicating that both of these strains might represent a novel species. The highest level of zeaxanthin production was achieved (YUAB-SO-11, 1.20?±?0.11 mg g?1) and (YUAB-SO-45, 1.02?±?0.13 mg g?1) when cultivated in marine broth supplemented with 2 % NaCl (pH 7) and incubated at 30 °C. Addition of 0.1 M glutamic acid, an intermediate of citric acid cycle, enhanced the zeaxanthin production as 18 and 14 % by the strains YUAB-SO-11 and YUAB-SO-45 respectively. The zeaxanthin showed in vitro nitric oxide scavenging, inhibition of lipid peroxidation, and 2,2-diphenyl-1-picryl hydrazyl scavenging activities higher than the commercial zeaxanthin. The results of this study suggest that two novel strains YUAB-SO-11 and YUAB-SO-45 belonging to genus Muricauda produce zeaxanthin as a predominant carotenoid, and higher production of zeaxanthin was achieved on glutamic acid supplementation. The pigment showed good in vitro antioxidant activity, which can be exploited further for commercial applications. 相似文献