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61.
Deepak K. Pattanayak B. T. Rao T. R. Rama Mohan 《Journal of Sol-Gel Science and Technology》2011,59(3):432-447
This paper reviews selected aspects of research work carried out in bioceramics and bioceramic composites at the Ceramics
Laboratory IIT, Bombay, India. The focus here is in understanding and developing calcium hydroxyapatite (HA) bioceramics and
biocomposites, including calcium hydroxyapatite-titanium (HA-Ti) and calcium hydroxyapatite-polymethylmethacrylate (HA-PMMA).
Research involving apatite-wollastonite (AW) bioglass ceramics and bioceramic composites of AW with titanium as well as with
polymethylmethacrylate will be presented in a future article. HA powders were precipitated from solutions with varying Ca/P
ratios and calcined at a range of temperatures to investigate their structural evolution. HA-Ti composites were prepared by
powder metallurgical processes using HA powders calcined at 400 °C, followed by compaction at 600 MPa and subsequent sintering
at 1,000–1,200 °C. HA-PMMA composites containing up to 40 wt% PMMA were prepared by hot pressing at 150 °C and 150 MPa pressure.
The phases present in the various materials were identified by X-ray diffraction (XRD) and functional groups by FTIR, while
the sample morphologies were investigated by SEM. The bioactivity of the composites was evaluated by soaking them in simulated
body fluid (SBF) for 7 days, to evaluate their apatite-forming ability (a key indicator of bioactivity). The results obtained
are interpreted to aid in the development of “design rules” for the use of such biocomposite materials in specific biomedical
application. 相似文献
62.
Cho DS Gibson SC Bhandari D McNally ME Hoffman RM Cook KD Song L 《Rapid communications in mass spectrometry : RCM》2011,25(23):3575-3580
Batch slurry reactions are widely used in the industrial manufacturing of chemicals, pharmaceuticals, petrochemicals and polymers. However, onsite monitoring of batch slurry reactions is still not feasible in production plants due to the challenge in analyzing heterogeneous samples without complicated sample preparation procedures. In this study, direct analysis in real time mass spectrometry (DART-MS) has been evaluated for the onsite monitoring of a model batch slurry reaction. The results suggested that automation of the sampling process of DART-MS is important to achieve quantitative results. With a sampling technique of manual sample deposition on melting point capillaries followed by automatic sample introduction across the helium beam, relative standard deviation (RSD) of the protonated molecule signals from the reaction product of the model batch slurry reaction ranged from 6 to 30%. This RSD range is improved greatly over a sampling technique of manual sample deposition followed by manual sample introduction where the RSDs are up to 110%. Furthermore, with the semi-automated sampling approach, semi-quantitative analysis of slurry samples has been achieved. Better quantification is expected with a fully automated sampling approach. 相似文献
63.
Tak V Pardasani D Purohit A Dubey DK 《Rapid communications in mass spectrometry : RCM》2011,25(22):3411-3416
The retrospective detection and identification of degradation products of chemical warfare agents are of immense importance in order to prove their spillage and use. A highly sensitive liquid chromatography/electrospray ionization tandem mass spectrometric (LC/ESI-MS/MS) method--using an imidazolium-based tricationic reagent--was developed for the detection and identification of the anionic degradation products of nerve agents. A commercially available solution of 1,3-imidazolium-bis-(1-hexylbenzylimidazolium) trifluoride (IBHBI) formed adducts with alkylphosphonic acids (APAs), allowing detection of the APAs by positive mode ESI-MS. Tandem mass spectrometry was used for the unambiguous identification of the APAs. Parameters influencing the formation and stability of these adduct during mass spectrometric analysis, such as solvent composition, concentration of IBHBI, effect of pH and interferences by salts, were optimized. The absolute limits of detection (0.1 ng) for achieved for the APAs were better than those previously reported, and linear dynamic ranges of 10-2000 ng mL(-1) were achieved. The method was repeatable with a relative standard deviation ≤7.3%. APAs present in aqueous samples provided by the Organization for the Prohibition of Chemical Weapons during the 22(nd) and 24(th) Official Proficiency tests were detected and identified as IBHBI adducts. The added advantage of this method is that low-mass analytes are detected at higher mass, thus obviating the problem with background noise at low mass. 相似文献
64.
A general rate model was employed in concert with a preferential interaction quadratic adsorption isotherm for the characterization of HIC resins and the prediction of solute behavior in these separation systems. The results indicate that both pore and surface diffusion play an important role in protein transport in HIC resins. The simulated and experimental solute profiles were compared for two model proteins, lysozyme and lectin, for both displacement and gradient modes of chromatography. Our results indicate that a modeling approach using the generate rate model and preferential interaction isotherm can accurately predict the shock layer response in both gradient and displacement chromatography in HIC systems. While pore and surface diffusion played a major role and were limiting steps for proteins, surface diffusion was seen to play less of a role for the displacer. The results demonstrate that this modeling approach can be employed to describe the behavior of these non-linear HIC systems, which may have implications for the development of more efficient preparative HIC separations. 相似文献
65.
Sukul PK Asthana D Mukhopadhyay P Summa D Muccioli L Zannoni C Beljonne D Rowan AE Malik S 《Chemical communications (Cambridge, England)》2011,47(43):11858-11860
We report unique and spontaneous formation of hydrogels of perylene derivatives with melamine. The luminescent gel network is formed by H-type aggregation of the perylene core, supramolecularly cross-linked by melamine units. As a result of controlled aggregation in the extended nanofibers, strong exciton fluorescence emission is observed. 相似文献
66.
DNA block copolymer doing it all: from selection to self-assembly of semiconducting carbon nanotubes
67.
Pardasani D Tak V Purohit AK Kanaujia PK Dubey DK 《European journal of mass spectrometry (Chichester, England)》2011,17(1):57-64
Gas chromatography-mass spectrometry (GC-MS) analysis of O,O'-dialkyl methylphosphonites (DAMPs) was carried out with a view to developing a database and understanding the mechanism of fragmentation. DAMPs are included in the list of schedule 2B4 chemicals of the Chemical Weapons Convention. GC-MS analysis of DAMPs and their deuterated analogs revealed that their fragmentations were dominated by α-cleavages, alkenyl radical loss and hydrogen rearrangements. Based on fragment ions of deuterated analogs and density functional theory calculations, the fragmentation routes were rationalized. 相似文献
68.
Set-Valued and Variational Analysis - The epsilon-subdifferential of convex univariate piecewise linear-quadratic (PLQ) functions can be computed in linear worst-case time complexity as the... 相似文献
69.
We study the efficiency of the incomplete enumeration algorithm for linear and branched polymers. There is a qualitative difference
in the efficiency in these two cases. The average time to generate an independent sample of configuration of polymer with
n monomers varies as n
2 for linear polymers for large n, but as exp(cn
α) for branched (undirected and directed) polymers, where 0<α<1. On the binary tree, our numerical studies for n of order 104 gives α = 0.333±0.005. We argue that α =1/3 exactly in this case.
An erratum to this article can be found at . 相似文献
70.
Complexes of the general formula [ReIII(L)Cl(PPh3)2] have been synthesised by reacting H2L and [ReOCl3(PPh3)2] in ethanol. Here H2L represents imines of α-amino acids (glycine, l-alanine, l-valine, l-phenylalanine) derived from salicylaldehyde and naphthaldehyde. The crystal structure of one complex has been determined. The complexes are mononuclear, paramagnetic and display paramagnetic 1H NMR in CDCl3 solution. Their spectral and redox properties are scrutinised. 相似文献