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排序方式: 共有812条查询结果,搜索用时 109 毫秒
1.
A. Ray R. Sriravindrarajah J.-P. Guerbois P. S. Thomas S. Border H. N. Ray J. Haggman P. Joyce 《Journal of Thermal Analysis and Calorimetry》2007,88(1):279-283
The use of supplementary cementitious materials (SCM) is a well established practice worldwide in the manufacture of Portland cement (PC)-based construction materials. While utilisation of industrial by-products has been successful, the potential of mining wastes is yet to receive adequate attention in the context of construction materials. In an expanded form perlite, which is a naturally occurring, hydrated volcanic siliceous glass, is an ideal material as a lightweight aggregate for use in a wide range of construction materials including concrete. The mining and processing of the grades of perlite required for the production of lightweight aggregate results in the creation of a fine grained waste which currently has no economic value. This paper reports preliminary data on the utilisation of waste perlite fines as a SCM in calcium silicate-based construction material and discusses the potential of this mining waste to reduce the environmental impact of the production of conventional cement-based construction materials. 相似文献
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Alexopoulos T Allen C Anderson EW Areti H Banerjee S Beery PD Biswas NN Bujak A Carmony DD Carter T Cole P Choi Y De Bonte RJ Erwin AR Findeisen C Goshaw AT Gutay LJ Hirsch AS Hojvat C Kenney VP Lindsey CS LoSecco JM McMahon T McManus AP Morgan N Nelson KS Oh SH Piekarz J Porile NT Reeves D Scharenberg RP Stampke SR Stringfellow BC Thompson MA Turkot F Walker WD Wang CH Wesson DK 《Physical review letters》1990,64(9):991-994
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Kochocki JA Allison WW Alner GJ Ambats I Ayres DS Balka LJ Barr GD Barrett WL Benjamin D Border P Brooks CB Cobb JH Cockerill DJ Coover K Courant H Dahlin B DasGupta U Dawson JW Edwards VW Fields TH Kirby-Gallagher LM Garcia-Garcia C Giles RH Goodman MC Heller K Heppelman S Hill N Hoftiezer JH Jankowski DJ Johns K Joyce T Kafka T Litchfield PJ Lopez FV Lowe M Mann WA Marshak ML May EN McMaster L Milburn RH Miller W Napier A Oliver WP Pearce GF Perkins DH Peterson EA Price LE Roback D Rosen DB 《Physical review D: Particles and fields》1990,42(9):2967-2973
6.
Mathiazhagan C Molzon WR Cousins RD Konigsberg J Kubic J Melese P Rubin P Slater WE Wagner D Hart GW Kinnison WW Lee DM McKee RJ Milner EC Sanders GH Ziock HJ Arisaka K Knibbe P Urheim J Axelrod S Biery KA Irwin GM Lang K Margulies J Ouimette DA Ritchie JL Trang QH Wojcicki SG Auerbach LB Buchholz P Highland VL McFarlane WK Sivertz M Chapman MD Eckhause M Ginkel JF Hancock AD Joyce D Kane JR Kenney CJ Vulcan WF Welsh RE Whyley RJ Winter RG 《Physical review letters》1989,63(20):2181-2184
7.
A highly sensitive and selective liquid chromatography-mass spectrometry (LC-MS) method has been developed for the determination of epirubicin in serum and cell specimens using daunorubicin as an internal standard. Using atmospheric pressure chemical ionisation (APCI), the epirubicin metabolites were readily distinguishable by their fragmentation pattern in the mass spectrometer. Selected reaction monitoring (SRM) mode was employed for quantitation of epirubicin and the metabolites. Following extraction, chromatography was performed on a C18 column with a mobile phase consisting of water-acetonitrile-formic acid, pH 3.2, with a flow rate of 200 μl/min. The limit of detection (LOD) and the limit of quantitation (LOQ) of this method in serum were determined to be 1.0 and 2.5 ng/ml, respectively. Linearity of the method was verified over the concentration range of 2.5-2000 ng/ml, with a high correlation coefficient (R2 ≥ 0.998). For the extraction procedure, an aliquot of 500 μl serum, spiked with internal standard, was extracted using a chloroform-2-isopropanol (2:1, v/v) mixture. The method has been applied to the analysis of epirubicin in cancer cell samples and the identification of known and unknown metabolites in clinical trial patient serum samples. 相似文献
8.
R. L. S. Devine C. T. Foxon B. A. Joyce J. B. Clegg J. P. Gowers 《Applied Physics A: Materials Science & Processing》1987,44(2):195-200
Beryllium diffusion during MBE growth of (Al, Ga)As layers, (Al, Ga)As/GaAs heterojunctions and GaAs/AlAs superlattices has been studied by electrochemical C-V and secondary ion mass spectrometry (SIMS) concentration profiling, in conjunction with transmission electron microscopy. Diffusion times were comparatively short since they were limited to part of the growth sequence, so non-equilibrium effects had a significant influence. The results are consistent with an interstitial-substitutional mechanism in which lattice site incorporation becomes more difficult with increasing band gap enthalpy. Incorporation involves a kick-out reaction which leads to the observed disordering of the superlattices. 相似文献
9.
A simple and efficient preparation of gramicidin S and its analogues is described. It involves solid-phase peptide synthesis and on-resin macrolactamization without side chain protection, affording cyclic products in high yield and high purity. The high specificity of the cyclization reaction was shown to originate in the formation of a pre-organized conformation of the linear biosynthetic precursor of gramicidin S. This facile method will provide convenient access to the analogues of the natural product for functional optimization to counter microbial resistance. 相似文献
10.
W.John Albery Philip N. Bartlett Andrew J. McMahon 《Journal of Electroanalytical Chemistry》1985,182(1):7-23
Results are reported for the reaction of methylviologen radical cation, MV+ with platinum colloidal particles, studied by stopped flow spectrophotometry. The rate of the reaction depends on the gaseous pretreatment of the particles. For particles reduced by hydrogen, the kinetics are usually first order with respect to MV+. The reaction is also first order in the concentration of platinum, and is inhibited in a first order manner by the product MV2+. This inhibition suggests that MV2+ is adsorbed on the particle surfaces, and this has been confirmed by ac, ring—disc electrode studies on macroscopic platinum electrodes. At high concentrations of MV+ some deviation from first order kinetics is observed. These results are all explained by a kinetic model in which either the desorption of MV2+ or the adsorption of MV+ is the rate limiting process. The rate of consumption of MV+ on an oxidised surface is an order of magnitude faster than that on the reduced surface. Ring—disc studies show that this is because the MV+ is not producing H2 but is reducing the surface oxide. The results are shown to fit a simple model which takes into account this titration of the oxide layer. The model also explains why the rate on partially oxidised surfaces will appear to have an order greater than one in [Pt]. 相似文献