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81.
In distributed systems, user authentication schemes based on password and smart card are widely used to ensure only authorized access to the protected services. Recently, Chang et al. presented an untraceable dynamic-identity-based user authentication scheme with verifiable-password-update. In this research, we illustrate that Chang et al.’s scheme violates the purpose of dynamic-identity contrary to authors’ claim. We show that once the smart card of an arbitrary user is lost, passwords of all registered users are at risk. Using information from an arbitrary smart card, an adversary can impersonate any user of the system. In addition, its password change phase has loopholes and is misguiding. The scheme has no provision for session key agreement and the smart card lacks any verification mechanism. Then we come-up with an improved remote user authentication scheme with the session key agreement, and show its robustness over related schemes. 相似文献
82.
The electrochemical behavior of Li/V6O13 cells is investigated at room temperature (22 °C) both in liquid electrolyte consisting of oligomeric poly(ethyleneglycol)dimethylether+lithium bis(trifluoromethylsulfonylimide) and composite electrolytes formed by blending the liquid electrolyte with silica nanoparticles (fumed silica). The addition of fumed silica yields a gel-like electrolyte that demonstrates the desirable property of suppressing lithium dendrite growth due to the rigidity and immobility of the electrolyte structure. The lithium/electrolyte interfacial resistance for composite gel electrolytes is less than that for the corresponding base-liquid electrolyte, and the charge-discharge cycle performance and electrochemical efficiency for the Li/V6O13 cell is significantly improved. The effect of fumed silica surface group on the electrochemical performance is discussed; the native hydrophilic silanol surface group appears better than fumed silica that is modified with a hydrophobic octyl surface moiety. 相似文献
83.
Mohammed Mahfooz Khan 《Fuel》1982,61(6):553-556
This Paper deals with a comparative study on the use of gel permeation chromatography (g.p.c.) and vapour pressure osmometry (v.p.o.) to obtain molecular weight data for the hexane-soluble fractions of three H-coal liquids. The use of two types of column packing materials, polyvinylacetate and styrene-divinylbenzene copolymer gels, is described. A successful, preparative use of the polyvinylacetate gel to fractionate the hexane-soluble fraction of H-coal liquid, atmospheric still overhead (ASO), has been established. Molecular weight data obtained by v.p.o. for the benzene-soluble fraction and the pyridine-soluble fraction of the three H-coal liquids are reported. Solvent extraction has been utilized also to find the amount of oil, asphaltenes and asphaltols in the three H-coal liquids. 相似文献
84.
M. Rashid Khan 《Fuel》1989,68(12):1522-1531
Coal devolatilization studies to maximize the yield of condensable products by operating at elevated temperatures and heating rates have been published. The objectives of this study were to investigate the influences of relatively mild operating conditions (e.g. relatively low temperature and pressure) on product quality, by comparing devolatilized products obtained at various temperatures and heating rates. Fixed bed, fluid bed, and entrained flow reactor units were used to obtain pyrolysis products. In addition, literature data on tar yields in various reactor units at a range of temperatures and residence times were surveyed and compared with experimental data. The liquids were characterized by a number of techniques, including field ionization mass spectroscopy (f.i.m.s.), sequential elution solvent chromatography (s.e.s.c.) and elemental analysis. The results demonstrate that the quality and yield of liquids obtained at a rapid heating rate are functions of peak pyrolysis temperature. It was shown that at a rapid heating rate, the yields of heavier polyfunctional groups (i.e. hydrocarbons with greater mean molecular weight) are greater than those obtained in the fixed bed slow heating rate reactor. The liquids generated at a slow heating rate are of lower molecular weight, viscosity, and sulphur content, and of higher H/C atomic ratios compared with the liquids obtained in a rapid heating rate unit. The effect of increasing the maximum pyrolysis temperature (at a constant slow heating rate) was to increase the yield of light gases (mainly H) at the expense of char hydrogen content and char reactivity. The tar yield is not markedly influenced when the peak devolatilization temperature is increased at a relatively slow heating rate. However, the quality (as defined by the H/C (atomic) ratio) of the liquids, and the reactivity (in air) of char, was reduced when the peak pyrolysis temperature was increased. At a rapid heating rate, the primary products, which have many structural characteristics of the parent coal, are devolatilized. The quality of the liquids obtained at a rapid heating rate is, therefore, determined by the devolatilized primary coal fragments evolved at the devolatilization temperature. In a slow heating rate fixed bed unit, however, the primary coal fragments undergo additional cracking reactions which involve stabilization of free radicals by donatable hydrogen. This leads to the formation of low molecular weight hydrocarbons of relatively higher quality. In-situ (both intraparticle or extraparticle) stabilization of reactive coal fragments by donatable hydrogen may lead to a significant improvement in the overall quality of the pyrolysis liquids in a fixed bed system in which time-temperature history is conducive for such reactions. 相似文献
85.
The solubility of many salts in water decreases dramatically with temperature in the vicinity of the critical point of pure water. Examples of these salts are sulfates of sodium, potassium, lithium and sodium carbonate. These salts are usually produced during supercritical water oxidation (SCWO) and contribute to fouling. The solubility of Na2CO3 and Na2SO4 has been determined in pure form and in the presence of each other, for the temperature range relevant to SCWO. The experimental procedure was to pass the salt solution through a tube at constant temperature. After a brief initiation period during which no salt sticks to the tube, the salt above the solubility limit deposited on the tube surface. The solution leaving the section was thus at the solubility limit. A rapid decrease in the salt solubility was observed just above the pseudo-critical temperature. For supercritical conditions, the solubility of each salt in the form of a mixture was quite close to the solubility of pure salt. At the highest fluid density considered (480 kg/m3) the presence of Na2CO3 reduces the solubility of Na2SO4, as might be expected from the “common-ion effect”. 相似文献
86.
Raina Aman Qazi Mohammad Saleem Khan Luqman Ali Shah Rizwan Ullah Ayesha Kausar Rozina Khattak 《Polymer-Plastics Technology and Engineering》2020,59(9):928-951
ABSTRACTFabrication of electronic materials from nanocomposite of biopolyesters reinforced with carbon nanotubes can be regarded as the effective alternative for conventional nanocomposites consisting of non-biodegradable polymers. Commercial availability of biopolyester-based nanocomposites is limited because of their high cost compared to other polymers, but the factor of their compostable nature is worthless for environmental protection. Such nanocomposites have potential applications in biodegradable sensors, EMI materials, etc. In this review, the current progress of biopolyester/CNTs nanocomposites in the field of biodegradable electronics is reviewed and also the impact of CNTs dispersion on electrical, thermal and mechanical properties of eco composites is stipulated. 相似文献
87.
Huiquan Wu Mansoor A. Khan Ajaz S. Hussain - Current address: Global Biopharmaceutical Development Sandoz Princeton New Jersey. 《Chemical Engineering Communications》2007,194(6):760-779
FDA's Process Analytical Technology (PAT) initiative provides an unprecedented opportunity for chemical engineers to play significant roles in the pharmaceutical industry. In this article, the authors provide their perspectives on (1) the need for chemical engineering principles in pharmaceutical development for a thorough process understanding; (2) applications of chemical engineering principles to meet the challenges from the semiconductor and pharmaceutical industries; and (3) the integration of chemical engineering practice into the semiconductor and pharmaceutical industries to achieve process understanding and the desired state of quality-by-design. A real-world case study from the semiconductor industry is presented to demonstrate how a classic chemical engineering concept, mixing homogeneity, can be implemented by inducing forced flow to ensure an excellent copper electrochemical plating process performance and to improve product quality substantially. Further, a case study of brake system design is discussed with the concept of Dr. Taguchi's robust engineering design to illustrate how quality-by-design can be achieved through appropriate experimental design, in conjunction with the discussion on the concept of quality-by-design in pharmaceuticals. Third, a case study of freeze-dried sodium ethacrynate is presented to demonstrate the vital importance of controlling the processing factors to achieve the desired product stability. Finally, the problems of the current pharmaceutical manufacturing mode, the opportunities and engineering challenges during implementation of PAT in the pharmaceutical industry, and the role of chemical engineering in implementation of PAT is discussed in detail. 相似文献
88.
[60]Fullerene (C60) was mono-substituted with well-defined poly(methyl methacrylate) (PMMA-b-C60) using the atom transfer radical polymerization (ATRP) technique. The self-assembly behaviors of PMMA-b-C60 in ethyl acetate (EA) and decalin mixtures were studied using laser light scattering (LLS) and transmission electron microscopy (TEM). Homogeneous solutions of PMMA-b-C60 can be obtained in the solvent mixtures containing more than 40 wt% EA, where the molar ratio of decalin to EA is close to 1. For each solvent mixture, unimers coexist with micelles and large aggregates. The sizes of PMMA-b-C60 micelles and aggregates are independent of polymer concentration, confirming that they are produced via the closed association mechanism. For the various solvent mixtures, the weight-averaged molecular weights, Mw of the PMMA-b-C60 aggregates range from 4.1×107 to 12.5×107 g/mol. The hydrodynamic radii of the large aggregate, Rh, vary from 90 to 136 nm, while the z-averaged radii of gyration, Rg, range from 210 to 311 nm. The Rg/Rh value for each solvent mixture is ∼2.3, which is independent of decalin contents in the mixed solvents. The morphological study using the transmission electron microscope suggests that the large aggregates are composed of porous large compound micelles (LCM) in solution. 相似文献
89.
90.
Huong Thi Le Inge D Brouwer Jan Burema Khan Cong Nguyen Frans J Kok 《Nutrition journal》2006,5(1):1-8